# Copyright (c) 1966-2018 Johns Hopkins University. Use of this file adheres to the terms specified at https://omim.org/help/agreement.																	
# Generated: 2018-04-09																	
# See end of file for additional documentation on specific fields																	
# Chromosome	Genomic Position Start	Genomic Position End	Cyto Location	Computed Cyto Location		Mim Number	Gene Symbols	Gene Name	Approved Symbol	Entrez Gene ID	Ensembl Gene ID	Comments	Phenotypes	Mouse Gene Symbol/ID	Inheritance	Clinical Synopsis	
chr1	0	27600000	1p36			607413	AD7CNTP	Alzheimer disease neuronal thread protein									
chr1	0	27600000	1p36		%	612367	ALPQTL2	"Alkaline phosphatase, plasma level of, QTL 2"		100196914		linkage with rs1780324	"{Alkaline phosphatase, plasma level of, QTL 2}, 612367 (2)"		NA		
chr1	0	123400000	1p		%	606788	ANON1	"Anorexia nervosa, susceptibility to, 1"		171514			"{Anorexia nervosa, susceptibility to, 1}, 606788 (2)"		NA		
chr1	0	27600000	1p36		%	605462	BCC1	"Basal cell carcinoma, susceptibility to, 1"		100307118		associated with rs7538876	"{Basal cell carcinoma, susceptibility to, 1}, 605462 (2)"		NA		
chr1	0	27600000	1p36		%	606928	BMND3	Bone mineral density QTL 3		246259		?another locus at 3p21	"[Bone mineral density QTL 3], 606928 (2)"		NA		
chr1	0	27600000	1p36		%	155600	"CMM, MLM, DNS"	Cutaneous malignant melanoma/dysplastic nevus	CMM	1243		some linkage studies negative; see 9p	"{Melanoma, cutaneous malignant, 1}, 155600 (2), Autosomal dominant"		AD	"INHERITANCE
- Autosomal dominant 
HEAD & NECK
Eyes
- Intraocular melanoma 
SKIN, NAILS, & HAIR
Skin
- Atypical nevi (>5mm with irregular edge and pigmentation) 
- Numerous nevi 
- Atypical nevi often present in non-sun exposed areas 
NEOPLASIA
- Malignant melanoma "	
chr1	0	20100000	1pter-p36.13		%	115665	"CTRCT8, CCV"	"Cataract, congenital, Volkmann type"	CCV	7792		linked to Rh in Scottish family	"Cataract 8, multiple types, 115665 (2), Autosomal dominant"		AD	"EYES
- Congenital cataract 
- Progressive visual loss 
INHERITANCE
- Autosomal dominant "	
chr1	0	27600000	1p36		#	607872	"DEL1p36, C1DELp36"	Chromosome 1p36 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 1p36 deletion syndrome, 607872 (4), Isolated cases"		IC	"INHERITANCE
- Isolated cases 
GROWTH
Weight
- Obesity (after infancy) 
Other
- Growth retardation, pre- and postnatal 
HEAD & NECK
Head
- Microcephaly 
- Brachycephaly 
- Large anterior fontanel 
- Delayed closure of fontanel 
Face
- Prominent forehead 
- Midface hypoplasia 
- Pointed chin 
- Long philtrum 
Ears
- Asymmetric ears 
- Sensorineural hearing loss 
- Thickened helices 
- Posteriorly rotated ears 
- Low-set ears 
Eyes
- Deep-set eyes 
- Hypermetropia 
- Visual inattentiveness 
- Strabismus 
- Myopia 
- Nystagmus 
- Optic nerve coloboma 
- Epicanthal folds 
- Straight eyebrows 
Nose
- Flat nasal bridge 
- Flat nose 
Mouth
- Cleft lip 
- Cleft palate 
- Submucous cleft 
- Bifid uvula 
- High-arched palate 
CARDIOVASCULAR
Heart
- Dilated cardiomyopathy (infancy) 
- Noncompaction cardiomyopathy 
- Ventricular septal defect 
- Atrial septal defect 
Vascular
- Patent ductus arteriosus 
- Dilated aortic root 
CHEST
Ribs Sternum Clavicles & Scapulae
- Missing ribs 
- Bifid ribs 
- Fused ribs 
ABDOMEN
Gastrointestinal
- Gastroesophageal reflux (infancy) 
- Feeding problems (infancy) 
SKELETAL
- Flexion contractures 
Spine
- Scoliosis 
Hands
- Short fifth finger 
- Fifth finger clinodactyly 
- Brachydactyly 
Feet
- Pes cavus 
- Prominent heels 
- Brachydactyly 
- Short feet 
NEUROLOGIC
Central Nervous System
- Global developmental delay 
- Mental retardation 
- Delayed expressive language 
- Delayed speech 
- Seizures 
- Infantile spasms 
- Hypotonia 
- Hydrocephalus 
- Ventriculomegaly 
- Cerebral atrophy 
- Agenesis of the corpus callosum 
- Pachygyria 
- Polymicrogyria 
Behavioral Psychiatric Manifestations
- Behavioral disorders 
- Hyperphagia 
ENDOCRINE FEATURES
- Hypothyroidism 
LABORATORY ABNORMALITIES
- Partial terminal deletion of short arm of chromosome 1 (1p36) 
MISCELLANEOUS
- Variable phenotype 
- Contiguous gene deletion syndrome 
- Marked variability in the deletion size 
- Most common terminal deletion syndrome 
- Incidence of 1 in 5,000 to 1 in 10,000 
MOLECULAR BASIS
- A contiguous gene syndrome caused by deletion of 2.2 to 10.6Mb of terminal 1p36 "	
chr1	0	46300000	1p36-p34		%	608995	DYX8	"Dyslexia, susceptibility to, 8"	DYX8	406874		between D1S552 and D1S1622	"{Dyslexia, susceptibility to, 8}, 608995 (2), Autosomal dominant, Multifactorial"		"Mu, AD"	"INHERITANCE
- Autosomal dominant 
- Multifactorial 
NEUROLOGIC
Central Nervous System
- Dyslexia 
- Difficulty in spelling 
- Difficulty in phonologic coding 
- Decreased rapid automatized naming (RAN) speed "	
chr1	0	27600000	1pter-p36			131190	"ERPL1, HLM2"	Endogenous retroviral pol gene-like sequence 1 (oncogene HLM2)									
chr1	0	27600000	1p36		%	605225	IBD7	Inflammatory bowel disease 7	IBD7	57042		associated with rs6426833	"{Inflammatory bowel disease 7}, 605225 (2)"				
chr1	0	27600000	1p36		%	612596	MS4	"Multiple sclerosis, susceptibility to, 4"		100271696		associated with rs10492972	"{Multiple sclerosis, susceptibility to, 4}, 612596 (2)"				
chr1	0	27600000	1p36		%	610320	MYP14	Myopia 14	MYP14	100359407		between D1S552 and D1S1622	"Myopia 14, 610320 (2)"				
chr1	0	123400000	1p		%	605606	PSORS7	Psoriasis susceptibility 7	PSORS7	65245			"{Psoriasis susceptibility 7}, 605606 (2)"				
chr1	0	7100000	1p36.3			604008	PTPRZ2	"Protein-tyrosine phosphatase, receptor-type, zeta-2"	PTPRZ2	5804							
chr1	0	94300000	1pter-p22.1			154280	"SAI1, MTS1, TFS1"	Suppression of anchorage independence-1 (malignant transformation suppression-1)	SAI1	6298							
chr1	0	27600000	1p36		#	607317	"SCAR4, SCASI"	"Spinocerebellar ataxia, autosomal recessive 4"	SCASI	260415			"Spinocerebellar ataxia, autosomal recessive 4, 607317 (2), Autosomal recessive"		AR	"INHERITANCE
- Autosomal recessive 
HEAD & NECK
Head
- Microcephaly (in some patients) 
Eyes
- Difficulty reading 
- Overshooting horizontal saccades 
- Macrosaccadic oscillations 
- Increased velocity of larger saccades 
- Nystagmus 
SKELETAL
Feet
- Pes cavus 
MUSCLE, SOFT TISSUES
- Axial hypotonia 
- Distal muscle weakness 
- Distal muscle atrophy 
- Abnormal mitochondria seen on muscle biopsy
NEUROLOGIC
Central Nervous System
- Delayed motor development (in some patients) 
- Intellectual disability, mild (in some patients) 
- Cerebellar ataxia 
- Ataxic gait 
- Frequent falls 
- Abnormal gait 
- Dysarthria 
- Spasticity 
- Pyramidal tract signs 
- Dystonia 
- Hyperreflexia 
- Tremor 
- Extensor plantar responses 
- Myoclonus (in some patients) 
- Fasciculations 
- cerebellar atrophy seen on brain imaging (in some patients)
- Basal ganglia abnormalities (in some patients)
- White matter abnormalities (in some patients) 
Peripheral Nervous System
- Impaired distal sensation 
- Sensorimotor axonal neuropathy 
MISCELLANEOUS
- Variable age at onset (range infancy to adulthood) 
- Variable severity 
- Some patients become wheelchair-bound in adulthood
MOLECULAR BASIS
- Caused by mutation in the vacuolar protein sorting 13, yeast, homolog of, D (VPS13D, 608877.0001)
"	
chr1	925740	944580	1p36.33	1p36.33		616765	"SAMD11, MRS"	Sterile alpha motif domain-containing protein 11	SAMD11	148398	ENSG00000187634			Samd11 (MGI:2446220)			
chr1	944202	959298	1p36.33	1p36.33		610770	"NOC2L, NIR"	"Nucleolar complex-associated protein 2, S. cerevisiae, homolog of"	NOC2L	26155	ENSG00000188976			Noc2l (MGI:1931051)			
chr1	975197	982116	1p36.33	1p36.33		615921	"PERM1, C1orf170"	"PPARGC1-and ESRR-induced regulator, muscle, 1"	PERM1	84808	ENSG00000187642						
chr1	998961	1001051	1p36.31	1p36.33		608060	HES4	"Hairy/enhancer of split, Drosophila, homolog of, 4"	HES4	57801	ENSG00000188290						
chr1	1013466	1014539	1p36.33	1p36.33	*	147571	"ISG15, G1P2, IFI15, IMD38"	ISG15 ubiquitin-like modifier	ISG15	9636	ENSG00000187608		"Immunodeficiency 38, 616126 (3), Autosomal recessive"	Isg15 (MGI:1855694)	AR	"INHERITANCE
- Autosomal recessive 
HEAD & NECK
Face
- Herpetic lesions (in 1 patient) 
SKIN, NAILS, & HAIR
Skin
- Necrotic skin ulcers (in 1 patient) 
NEUROLOGIC
Central Nervous System
- Basal ganglia calcifications 
- Calcification along the cerebral falx 
- Seizures (in one patient) 
- Normal psychomotor development 
IMMUNOLOGY
- Susceptibility to mycobacterial disease 
- Lymphadenopathy subsequent to BCG vaccination 
- Lymphadenitis subsequent to BCG vaccination (in 1 patient) 
- No severe viral infections 
MISCELLANEOUS
- Based on report of 2 Iranian siblings, 1 Turkish patient, and 1 Chinese family (last curated October 2017) 
MOLECULAR BASIS
- Caused by mutation in the ISG15 ubiquitin-like modifier gene (ISG15, 147571.0001)
"	
chr1	1020101	1056118	1pter-p32	1p36.33	*	103320	"AGRN, CMS8"	Agrin	AGRN	375790	ENSG00000188157		"Myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, 615120 (3), Autosomal recessive"	Agrn (MGI:87961)	AR	"INHERITANCE
- Autosomal recessive 
HEAD & NECK
Face
- Facial weakness 
Eyes
- Ptosis 
- Extraocular muscle weakness, mild (1 patient) 
Mouth
- High-arched palate (1 patient) 
RESPIRATORY
- Respiratory insufficiency (1 patient) 
CHEST
External Features
- Narrow thorax 
MUSCLE, SOFT TISSUES
- Muscle weakness, proximal 
- Muscle weakness may affect upper limbs 
- Easy fatigability 
- Inability to run 
- Type II fiber atrophy seen on muscle biopsy 
- Fragmentation of the neuromuscular junction with pre- and postsynaptic defects 
- Small or absent axon terminals 
- Small endplate 
- Decrement of the compound muscle action potential on repetitive stimulation
MISCELLANEOUS
- Onset in early childhood 
- Variable severity 
- Two families have been reported (last curated April 2014) 
MOLECULAR BASIS
- Caused by mutation in the agrin gene (AGRN, 103320.0001)"	
chr1	1167103	1167197	1p36.33	1p36.33		612091	"MIR200B, MIRN200B"	Micro RNA 200B	MIR200B	406984							
chr1	1167862	1167951	1p36.33	1p36.33		612090	"MIR200A, MIRN200A"	Micro RNA 200A	MIR200A	406983							
chr1	1169004	1169086	1p36.33	1p36.33		612094	"MIR429, MIRN429"	Micro RNA 429	MIR429	554210							
chr1	1203507	1207900	1p36.3	1p36.33		603905	"TNFRSF18, AITR, GITR"	"Tumor necrosis factor receptor superfamily, member 18"	TNFRSF18	8784	ENSG00000186891			Tnfrsf18 (MGI:894675)			
chr1	1211325	1216811	1p36	1p36.33	*	600315	"TNFRSF4, TXGP1L, OX40, ACT35, IMD16"	"Tumor necrosis factor receptor superfamily, member 4"	TNFRSF4	7293	ENSG00000186827	mutation identified in 1 IMD16 family	"?Immunodeficiency 16, 615593 (3), Autosomal recessive"	Tnfrsf4 (MGI:104512)	AR	"INHERITANCE
- Autosomal recessive 
SKIN, NAILS, & HAIR
Skin
- Kaposi sarcoma, human herpes virus-8 (HHV8)-associated 
IMMUNOLOGY
- Impaired memory CD4+ T cell response to recall antigens 
NEOPLASIA
- Kaposi sarcoma, HHV-8-associated 
MISCELLANEOUS
- Juvenile onset 
- Kaposi sarcoma lesions may be disseminated 
- One patient has been reported (last curated June 2016) 
MOLECULAR BASIS
- Caused by mutation in the tumor necrosis factor receptor superfamily, member 4 gene (TNFRSF4, 600315.0001)"	
chr1	1216907	1232066	1p36.33	1p36.33		614282	"SDF4, CAB45"	Stromal cell-derived factor 4	SDF4	51150	ENSG00000078808			Sdf4 (MGI:108079)			
chr1	1232248	1235040	1p36.3	1p36.33	*	615291	"B3GALT6, SEMDJL1, EDSSPD2"	"UDP-Gal:beta-Gal beta-1,3-galactosyltransferase polypeptide 6"	B3GALT6	126792	ENSG00000176022		"Ehlers-Danlos syndrome, spondylodysplastic type, 2, 615349 (3), Autosomal recessive; Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures, 271640 (3), Autosomal recessive"	B3galt6 (MGI:2152819)	AR;AR	"INHERITANCE
- Autosomal recessive 
GROWTH
Weight
- Low weight 
HEAD & NECK
Face
- Prominent forehead 
- Flat face 
Eyes
- Prominent eyes 
- Proptosis 
- Blue sclerae 
Mouth
- Long upper lip 
- Cleft palate (rare) 
CHEST
Ribs Sternum Clavicles & Scapulae
- Pectus excavatum (rare) 
SKELETAL
- Large joint laxity 
Spine
- Platyspondyly 
- Kyphoscoliosis 
- Anterior beak of vertebral body 
Pelvis
- Short ilia 
- Hip dislocation 
- Prominent lesser trochanter 
Limbs
- Restricted elbow movement 
- Elbow malalignment 
- Metaphyseal flaring 
- Epiphyseal dysplasia of femoral head 
Hands
- Spatulate finger 
- Finger laxity 
- Hand contracture (rare) 
- Advanced carpal ossification 
- Carpal fusion (rare) 
- Metacarpal shortening 
Feet
- Clubfeet 
SKIN, NAILS, & HAIR
Skin
- Doughy skin 
- Hyperextensible skin 
- Cutis laxa 
Hair
- Sparse hair 
NEUROLOGIC
Central Nervous System
- Hypotonia 
- Developmental delay (rare) 
MOLECULAR BASIS
- Caused by mutation in the UDP-Gal:beta-Gal beta-1,3-galactosyltransferase polypeptide 6 gene (B3GALT6, 615291.0007)"	"INHERITANCE
- Autosomal recessive 
GROWTH
Height
- Dwarfism 
Weight
- Low weight 
HEAD & NECK
Face
- Oval face 
- Flat midface 
- Prominent forehead 
- Micrognathia 
Eyes
- Prominent eyes 
- Blue sclera 
- Myopia 
- Congenital myopia 
- Lens dislocation 
- Proptosis 
Mouth
- Cleft palate (31% of patients) 
- High-arched palate (12% of patients) 
- Long philtrum 
- Long upper lip 
Neck
- Short neck 
CARDIOVASCULAR
Heart
- Atrial septal defect 
- Ventricular septal defect 
- Mitral insufficiency 
- Bicuspid aortic valve 
CHEST
External Features
- Thoracic asymmetry 
Ribs Sternum Clavicles & Scapulae
- Anterior flaring of ribs 
- Cupped ribs 
- 11 pairs of ribs 
SKELETAL
- Joint laxity 
- Joint dislocation 
- Spondyloepimetaphyseal dysplasia 
- Joint contractures 
- Osteoporosis 
- Spontaneous fractures 
Spine
- Progressive kyphoscoliosis 
- Ovoid vertebrae (infancy) 
- Platyspondyly (childhood) 
- Irregular endplates (childhood) 
- Gross spinal malalignment 
- Anterior beak of vertebral body 
- Scoliosis 
Pelvis
- Large, flared iliac wings 
- Hypoplastic iliac body 
- Narrow pubic bones 
- Delayed ossification of femoral capital epiphyses 
- Hip dislocation 
- Hip subluxation 
- Short femoral necks 
- Coxa valga 
- Prominent lesser trochanter 
Limbs
- Genu valga (80% of patients) 
- Radial head dislocation 
- Radial head subluxation 
- Radial bowing 
- Restricted elbow movement 
- Elbow malalignment 
- Short, slender long bones 
- Wide metaphyses 
- Metaphyseal flaring 
- Epiphyseal dysplasia of femoral head 
- Abnormal trabecular pattern 
Hands
- Hypermobile digits 
- Spatulate terminal phalanges (especially thumbs) 
- Short metacarpals 
- Hand contracture (rare) 
- Advanced carpal ossification 
- Carpal fusion (rare) 
Feet
- Talipes equinovarus 
- Pes planus 
- Hallux valgus 
- Metatarsus adductus 
SKIN, NAILS, & HAIR
Skin
- Soft, doughy skin 
- Mild skin hyperextensibility 
- Skin fragility 
- Atrophic scarring 
- Palmar wrinkling 
Nails
- Foreshortened nails 
Hair
- Sparse scalp hair 
NEUROLOGIC
Central Nervous System
- Spinal cord compression 
- Paraplegia 
- Hypotonia 
MISCELLANEOUS
- Common in Afrikaan population, South Africa 
- Death in first-second decade of life secondary to cardio-respiratory compromise 
MOLECULAR BASIS
- Caused by mutation in the UDP-Gal:beta-Gal beta-1,3-galactosyltransferase polypeptide 6 gene (B3GALT6, 615291.0001)"
chr1	1242445	1247217	1p36.33	1p36.33		616593	"FAM132A, C1QDC2, C1QTNF12"	"Family with sequence similarity 132, member A"	C1QTNF12	388581	ENSG00000184163			C1qtnf12 (MGI:1914639)			
chr1	1280435	1292028	1p36.3-p36.2	1p36.33		601328	SCNN1D	"Sodium channel, voltage-gated, type I, delta polypeptide"	SCNN1D	6339	ENSG00000162572						
chr1	1311584	1324686	1p36.33	1p36.33		611354	"CPSF3L, INTS11, RC68"	Cleavage and polyadenylation-specific factor 3-like	INTS11	54973	ENSG00000127054			Ints11 (MGI:1919207)			
chr1	1324756	1328895	1p36.33	1p36.33		615467	"GLTPD1, CPTP"	Glycolipid transfer protein domain-containing protein 1	CPTP	80772	ENSG00000224051			Cptp (MGI:1933107)			
chr1	1331323	1335319	1p36.33	1p36.33		605865	"TAS1R3, T1R3"	"Taste receptor type 1, member 3"	TAS1R3	83756	ENSG00000169962			Tas1r3 (MGI:1933547)			
chr1	1335277	1349141	1p36	1p36.33	*	601365	"DVL1, DRS2"	Dishevelled 1 (homologous to Drosophila dsh)	DVL1	1855	ENSG00000107404		"Robinow syndrome, autosomal dominant 2, 616331 (3), Autosomal dominant"	Dvl1 (MGI:94941)	 AD	"INHERITANCE
- Autosomal dominant 
GROWTH
Height
- Short stature (in some patients) 
HEAD & NECK
Head
- Macrocephaly 
Face
- Frontal bossing 
- High forehead 
- Midface hypoplasia 
- Long philtrum 
- Micrognathia (in some patients) 
Ears
- Conductive hearing loss (in some patients) 
- Sensorineural hearing loss (in some patients) 
- Abnormal ear shape (in some patients) 
- Abnormal ear position (in some patients) 
Eyes
- Hypertelorism 
- Prominent eyes 
Nose
- Short nose 
- Wide, low nasal bridge 
- Anteverted nares 
Mouth
- Triangular mouth 
- Thin upper lip 
- Gingival hyperplasia 
Teeth
- Dental anomalies 
- Malocclusion 
- Dental crowding 
CHEST
Ribs Sternum Clavicles & Scapulae
- Pectus anomalies 
ABDOMEN
External Features
- Umbilical hernia (in some patients) 
GENITOURINARY
External Genitalia (Male)
- Micropenis 
Internal Genitalia (Male)
- Cryptorchidism 
SKELETAL
- Osteosclerosis (in some patients) 
Skull
- Thickened calvaria (in some patients) 
Limbs
- Mesomelia (in some patients) 
- Undertubulated long bones (in some patients) 
Hands
- Brachydactyly 
- Clinodactyly 
- Broad thumbs 
- Hypoplastic distal phalanges 
Feet
- Brachydactyly 
- Broad first toes 
- Hypoplastic distal phalanges 
MISCELLANEOUS
- Onset at birth 
MOLECULAR BASIS
- Caused by mutation in the dishevelled 1 gene (DVL, 601365.0001)"	
chr1	1352688	1363540	1p36.33	1p36.33		617293	"MXRA8, ASP3"	Matrix remodeling-associated protein 8	MXRA8	54587	ENSG00000162576			Mxra8 (MGI:1922011)			
chr1	1373729	1375515	1p36.3	1p36.33		609183	"AURKAIP1, AKIP, AIP"	Aurora kinase A-interacting protein 1	AURKAIP1	54998	ENSG00000175756			Aurkaip1 (MGI:1913327)			
chr1	1385710	1399341	1p36.33	1p36.33		613482	CCNL2	Cyclin L2	CCNL2	81669	ENSG00000221978			Ccnl2 (MGI:1927119)			
chr1	1401895	1407312	1p36.3-p35.2	1p36.33		611833	MRPL20	Mitochondrial ribosomal protein L20	MRPL20	55052	ENSG00000242485			Mrpl20 (MGI:2137221)			
chr1	1435522	1442881	1p36.3	1p36.33		611901	"VWA1, WARP"	von Willebrand factor A domain-containing protein 1	VWA1	64856	ENSG00000179403			Vwa1 (MGI:2179729)			
chr1	1449688	1470157	1p36.33	1p36.33		617227	ATAD3C	"ATPase family, AAA domain-containing, member 3C"	ATAD3C	219293	ENSG00000215915						
chr1	1471731	1509465	1p36.33	1p36.33		612317	"ATAD3B, TOB3, KIAA1273"	"ATPase family, AAA domain-containing, member 3B"	ATAD3B	83858	ENSG00000160072						
chr1	1512142	1534686	1p36.33	1p36.33	*	612316	"ATAD3A, HAYOS"	"ATPase family, AAA domain-containing, member 3A"	ATAD3A	55210	ENSG00000197785	one family with AR inheritance reported	"Harel-Yoon syndrome, 617183 (3), Autosomal recessive, Autosomal dominant"	Atad3a (MGI:1919214)	"AR,?AD"	"INHERITANCE
- Autosomal dominant 
- Autosomal recessive (one family) 
HEAD & NECK
Head
- High forehead 
Face
- Frontal bossing 
- Micrognathia 
- Prognathia (family A) 
- Long face (family A) 
Eyes
- Optic atrophy 
- Deep-set eyes 
- Upslanting palpebral fissures 
- Myopia 
- Nystagmus 
- Esotropia 
Nose
- Small nose 
CARDIOVASCULAR
Heart
- Hypertrophic cardiomyopathy (in some patients) 
CHEST
External Features
- Pectus carinatum 
ABDOMEN
Gastrointestinal
- Feeding difficulties 
SKELETAL
Spine
- Scoliosis 
Pelvis
- Hip dysplasia 
Feet
- Foot deformities 
MUSCLE, SOFT TISSUES
- Hypotonia 
- Distal limb muscle atrophy 
- Mitochondrial respiratory enzymes deficiencies 
NEUROLOGIC
Central Nervous System
- Delayed psychomotor development 
- Intellectual disability 
- Speech delay 
- Inability to walk 
- Ataxia (family A) 
- Axial hypotonia 
- Limb spasticity 
- Absence seizures (family A) 
- Cerebellar atrophy (family A) 
Peripheral Nervous System
- Axonal neuropathy 
LABORATORY ABNORMALITIES
- Increased lactate 
- Methylglutaconic aciduria (in some patients) 
MISCELLANEOUS
- Onset in infancy 
- Five unrelated patients with de novo heterozygous mutations have been reported 
- Two sibs (family A) with a homozygous mutation have been reported (last curated November 2016) 
MOLECULAR BASIS
- Caused by mutation in the ATPase family, AAA domain-containing, member 3A gene (ATAD3A, 612316.0001)"	
chr1	1534777	1540359	1p36.33	1p36.33	*	616101	"TMEM240, C1orf70, SCA21"	Transmembrane protein 240	TMEM240	339453	ENSG00000205090		"Spinocerebellar ataxia 21, 607454 (3), Autosomal dominant"	Tmem240 (MGI:3648074)	 AD	"INHERITANCE
- Autosomal dominant 
HEAD & NECK
Eyes
- Microsaccadic pursuit 
- Slow saccades 
- Square wave jerks 
- Nystagmus 
NEUROLOGIC
Central Nervous System
- Delayed psychomotor development 
- Cognitive impairment 
- Mental retardation 
- Cerebellar ataxia 
- Gait ataxia 
- Limb ataxia 
- Postural tremor 
- Parkinsonism 
- Akinesia 
- Dysarthria 
- Scanning speech 
- Dysgraphia 
- Hyporeflexia 
- Extrapyramidal signs 
- Cogwheel rigidity 
- Tremor 
- Cerebellar atrophy 
Behavioral Psychiatric Manifestations
- Aggression 
- Apathy 
- Impulsivity 
- Executive dysfunction 
MISCELLANEOUS
- Variable age of onset (range 1 to 30 years) 
- Slowly progressive 
MOLECULAR BASIS
- Caused by mutation in the transmembrane protein 240 gene (TMEM240, 616101.0001)"	
chr1	1541672	1574881	1p36.33	1p36.33		617680	SSU72	"Ssu72, S. cerevisiae, homolof of"	SSU72	29101	ENSG00000160075			Ssu72 (MGI:1916241)			
chr1	1613729	1630609	1p36.32	1p36.33		611141	MIB2	"Mindbomb, Drosophila, homolog of, 2"	MIB2	142678	ENSG00000197530			Mib2 (MGI:2679684)			
chr1	1631680	1635637	1p36.3	1p36.33		603321	"MMP23B, MMP22"	Matrix metalloproteinase 23B	MMP23B	8510	ENSG00000189409			Mmp23 (MGI:1347361)			
chr1	1635225	1659618	1p36.3	1p36.33		176873	"CDK11B, CDC2L1, P58, CDK11"	Cyclin-dependent kinase 11B	CDK11B	984	ENSG00000248333						
chr1	1699938	1701807	1p36.3	1p36.33		603320	"MMP23A, MMP21, MIFR"	Matrix metalloproteinase 23A	MMP23A	8511							
chr1	1702382	1724564	1p36.3	1p36.33		116951	"CDK11A, CDC2L2"	Cyclin-dependent kinase 11A	CDK11A	728642	ENSG00000008128			Cdk11b (MGI:88353)			
chr1	1751231	1780508	1p36.33-p36.21	1p36.33		611616	NADK	NAD kinase	NADK	65220	ENSG00000008130			Nadk (MGI:2183149)			
chr1	1785284	1891116	1pter-p31.2	1p36.33	*	139380	"GNB1, MRD42"	"Guanine nucleotide-binding protein, beta polypeptide-1"	GNB1	2782	ENSG00000078369		"Leukemia, acute lymphoblastic, somatic, 613065 (3); Mental retardation, autosomal dominant 42, 616973 (3), Autosomal dominant"	Gnb1 (MGI:95781)	NA;AD		"INHERITANCE
- Autosomal dominant 
GROWTH
Other
- Failure to thrive 
- Poor overall postnatal growth 
HEAD & NECK
Eyes
- Strabismus 
- Nystagmus 
- Impaired smooth pursuit 
- Cortical visual impairment (in some patients) 
Mouth
- Cleft palate (in some patients) 
GENITOURINARY
Kidneys
- Hydronephrosis (in some patients) 
MUSCLE, SOFT TISSUES
- Hypotonia 
NEUROLOGIC
Central Nervous System
- Global developmental delay 
- Intellectual disability 
- Limb hypertonia 
- Seizures, variable types 
- Abnormal EEG 
MISCELLANEOUS
- Onset in infancy 
- Variable features 
- De novo mutation 
MOLECULAR BASIS
- Caused by mutation in the guanine nucleotide-binding protein, beta-1 gene (GNB1, 139380.0001)
"
chr1	1913750	1917293	1p36.33	1p36.33		610171	"CALML6, CAGLP"	Calmodulin-like 6	CALML6	163688	ENSG00000169885						
chr1	2019328	2030752	1p36.3	1p36.33	*	137163	"GABRD, GEFSP5, EIG10, EJM7"	"Gamma-aminobutyric acid (GABA) A receptor, delta"	GABRD	2563	ENSG00000187730		"{Epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to}, 613060 (3), Autosomal dominant; {Epilepsy, idiopathic generalized, 10}, 613060 (3), Autosomal dominant; {Epilepsy, juvenile myoclonic, susceptibility to}, 613060 (3), Autosomal dominant"	Gabrd (MGI:95622)	AD	"INHERITANCE
- Autosomal dominant 
NEUROLOGIC
Central Nervous System
- Seizures, generalized 
- Seizures, generalized, associated with fever 
- Febrile seizures 
- Generalized tonic-clonic seizures 
- Absence seizures 
- Myoclonic seizures 
- Partial seizures 
MISCELLANEOUS
- Highly variable phenotype 
- Onset of febrile seizures typically between 6 months and 6 years of age 
- Simple febrile seizures usually remit by age 6 years 
- Some patients have a more severe phenotype and have febrile and afebrile seizures after childhood (GEFS+) 
- Some patients have juvenile-onset myoclonic epilepsy 
MOLECULAR BASIS
- Susceptibility conferred by mutation in the gamma-aminobutyric acid receptor, delta gene (GABRD, 137163.0001)"	
chr1	2050469	2185398	1p36	1p36.33		176982	"PRKCZ, PKC2"	"Protein kinase C, zeta form"	PRKCZ	5590	ENSG00000067606			Prkcz (MGI:97602)			
chr1	2184456	2212719	1p36.33	1p36.33		615183	"C1orf86, FAAP20"	Chromosome 1 open reading frame 86	FAAP20	199990	ENSG00000162585			Faap20 (MGI:1914763)			
chr1	2228694	2310212	1p36.3	1p36.33-p36.32	*	164780	"SKI, SGS"	Avian sarcoma viral (v-ski) oncogene homolog	SKI	6497	ENSG00000157933	formerly mapped to 1q22-q24	"Shprintzen-Goldberg syndrome, 182212 (3), Autosomal dominant"	Ski (MGI:98310)	AD	"INHERITANCE
- Autosomal dominant 
HEAD & NECK
Head
- Dolichocephaly 
- Microcephaly 
Face
- High, prominent forehead 
- Maxillary hypoplasia 
- Micrognathia 
Ears
- Soft auricles 
- Low-set ears 
- Posteriorly rotated ears 
- Hearing loss, conductive (rare) 
Eyes
- Telecanthus 
- Hypertelorism 
- Proptosis 
- Strabismus 
- Downslanting palpebral fissures 
- Myopia 
- Ptosis 
- Shallow orbits 
Nose
- Upturned nose 
Mouth
- High palate 
- Narrow palate 
- Prominent lateral palatine ridge 
Teeth
- Malocclusion 
CARDIOVASCULAR
Heart
- Mitral valve prolapse 
- Aortic root dilation 
Vascular
- Vertebrobasilar artery tortuosity (rare) 
- Internal carotid artery tortuosity (rare) 
- Pulmonary artery root dilation (rare) 
RESPIRATORY
Airways
- Obstructive apnea 
CHEST
Ribs Sternum Clavicles & Scapulae
- Pectus excavatum 
- Pectus carinatum 
- Thin ribs 
- 13 pairs of ribs (rare) 
ABDOMEN
External Features
- Umbilical hernia 
- Abdominal wall weakness 
Gastrointestinal
- Gastroesophageal reflux (rare) 
GENITOURINARY
External Genitalia (Male)
- Inguinal hernia 
External Genitalia (Female)
- Inguinal hernia 
Internal Genitalia (Male)
- Cryptorchidism (rare) 
SKELETAL
- Joint laxity 
- Joint contractures 
- Osteopenia 
Skull
- Craniosynostosis 
- Large anterior fontanel 
Spine
- C1-C2 vertebral abnormality (fusion or subluxation) 
- Scoliosis 
Limbs
- Bowed long bones (rare) 
- Genu valgum (rare) 
- Radial head dislocation (rare) 
- Wide metaphyses (rare) 
Hands
- Arachnodactyly 
- Camptodactyly 
- Genu recurvatum 
Feet
- Metatarsus adductus 
- Talipes equinovarus 
- Pes planus 
SKIN, NAILS, & HAIR
Skin
- Hyperelastic skin 
MUSCLE, SOFT TISSUES
- Minimal subcutaneous fat 
NEUROLOGIC
Central Nervous System
- Hypotonia 
- Developmental delay 
- Mental retardation 
- Hydrocephalus 
- Arnold-Chiari type I malformation 
MOLECULAR BASIS
- Caused by mutation in the avian sarcoma viral (v-ski) oncogene homolog gene (SKI, 164780.0001)"	
chr1	2300000	20100000	1p36.32-p36.13		%	607671	DYT13	"Dystonia 13, torsion"	DYT13	93983			"Dystonia 13, torsion, 607671 (2), Autosomal dominant"		AD	"INHERITANCE
- Autosomal dominant 
HEAD & NECK
Eyes
- Blepharospasm 
Mouth
- Oromandibular dystonia 
Neck
- Torticollis 
SKELETAL
Limbs
- Upper limb dystonia 
NEUROLOGIC
Central Nervous System
- Cranial dystonia 
- Torsion dystonia 
- Dystonic posturing 
- Rapid, jerky movements 
- Tremor 
- Writer's cramp 
MISCELLANEOUS
- Average age of onset 15 years (range 4 to 40) 
- Focal or segmental onset in cranial-cervical area or upper limbs 
- May progress to other body regions after many years 
- Dopa-unresponsive 
- Relatively mild course 
"	
chr1	2300000	29900000	1p36.32-p35.3		%	606242	KONDS	"Kondoh syndrome (mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism)"		100653373		linked to rs966321 and rs1441834	"Kondoh syndrome, 606242 (2), Autosomal recessive"		AR	"INHERITANCE
- Autosomal recessive 
GROWTH
Height
- Short stature 
Other
- Prenatal-onset growth retardation 
HEAD & NECK
Head
- Microcephaly 
Eyes
- Ptosis 
Nose
- Pear-shaped nose 
- Narrow alae nasi 
- Long philtrum 
Mouth
- Thin upper lip 
SKELETAL
Limbs
- Knee contracture 
Hands
- Polydactyly, preaxial 
- Interphalangeal joint contractures 
SKIN, NAILS, & HAIR
Skin
- Atopic dermatitis 
Hair
- Sparse hair 
- Widow's peak 
- Thick eyebrows 
NEUROLOGIC
Central Nervous System
- Mental retardation"	
chr1	2404801	2412573	1p36.32	1p36.32		602859	"PEX10, NALD, PBD6A, PBD6B"	Peroxisome biogenesis factor 10	PEX10	5192	ENSG00000157911		"Peroxisome biogenesis disorder 6A (Zellweger), 614870 (3), Autosomal recessive; Peroxisome biogenesis disorder 6B, 614871 (3), Autosomal recessive"	Pex10 (MGI:2684988)			
chr1	2412480	2505529	1p36.32	1p36.32		612836	"PLCH2, PLCL4"	"Phospholipase C, eta-2"	PLCH2	9651	ENSG00000149527			Plch2 (MGI:2443078)			
chr1	2508530	2526627	1p36	1p36.32		606162	PANK4	Pantothenate kinase 4	PANK4	55229	ENSG00000157881			Pank4 (MGI:2387466)			
chr1	2528744	2530553	1p36.31	1p36.32		607348	HES5	"Hairy/enhancer of split, Drosophila, homolog of, 5"	HES5	388585	ENSG00000197921			Hes5 (MGI:104876)			
chr1	2556364	2565621	1p36.3-p36.2	1p36.32		602746	"TNFRSF14, HVEM, TR2"	"Tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)"	TNFRSF14	8764	ENSG00000157873			Tnfrsf14 (MGI:2675303)			
chr1	3021481	3022902	1p36.32	1p36.32		608535	"ACTRT2, ARPT2, ARPM2"	Actin-related protein T2	ACTRT2	140625	ENSG00000169717			Actrt2 (MGI:1920603)			
chr1	3068226	3438620	1p36.3	1p36.32		605557	"PRDM16, MEL1, LVNC8, CMD1LL"	PR domain-containing protein 16	PRDM16	63976	ENSG00000142611		"Cardiomyopathy, dilated, 1LL, 615373 (3), Autosomal dominant; Left ventricular noncompaction 8, 615373 (3), Autosomal dominant"	Prdm16 (MGI:1917923)			
chr1	3487941	3624769	1p36.3	1p36.32		604266	"MEGF6, EGFL3"	Multiple epidermal growth factor-like domains 6	MEGF6	1953	ENSG00000162591			Megf6 (MGI:1919351)			
chr1	3560694	3560789	1p36.32	1p36.32		615148	MIR551A	Micro RNA 551A	MIR551A	693135							
chr1	3624991	3630130	1p36.32	1p36.32		611460	"TPRG1L, FAM79A"	Tumor protein p63 regulated 1-like	TPRG1L	127262	ENSG00000158109			Tprgl (MGI:1915058)			
chr1	3630766	3650106	1p36.3	1p36.32		606040	WDR8	WD repeat-containing protein 8	WRAP73	49856	ENSG00000116213			Wrap73 (MGI:1891749)			
chr1	3652564	3736200	1p36	1p36.32		601990	TP73	p53-related protein	TP73	7161	ENSG00000078900	imprinted	?Neuroblastoma (1)	Trp73 (MGI:1336991)			
chr1	3772760	3775981	1p36	1p36.32		615242	"SMIM1, VEL"	Small integral membrane protein 1	SMIM1	388588	ENSG00000235169		"[Blood group, Vel system], 615264 (3), Autosomal recessive"	Smim1 (MGI:1916109)			
chr1	3812080	3857232	1p36.32	1p36.32		616690	"CEP104, GLYBP, KIAA0562, JBTS25"	"Centrosomal protein, 104kD"	CEP104	9731	ENSG00000116198		"Joubert syndrome 25, 616781 (3), Autosomal recessive"	Cep104 (MGI:2687282)			
chr1	3857266	3885428	1p36.3	1p36.32		601883	"DFFB, CAD, DFF2"	"DNA fragmentation factor, 40kD, beta subunit"	DFFB	1677	ENSG00000169598			Dffb (MGI:1196287)			
chr1	4654774	4792517	1p36.32	1p36.32		610972	"AJAP1, SHREW1"	Adherens junction-associated protein 1	AJAP1	55966	ENSG00000196581			Ajap1 (MGI:2685419)			
chr1	5300000	20100000	1p36.31-p36.13			614414	DFNB96	"Deafness, autosomal recessive 96"	DFNB96	100861440		between rs3817914 and rs477558	"Deafness, autosomal recessive 96, 614414 (2), Autosomal recessive"				
chr1	5862807	5992472	1p36	1p36.31		607215	"NPHP4, SLSN4"	Nephrocystin 4	NPHP4	261734	ENSG00000131697		"Nephronophthisis 4, 606966 (3), Autosomal recessive; Senior-Loken syndrome 4, 606996 (3), Autosomal recessive"	Nphp4 (MGI:2384210)			
chr1	5992297	6101192	1p36.3	1p36.31		601142	"KCNAB2, KCNA2B"	"Potassium voltage-gated channel, shaker-related subfamily, beta member 2"	KCNAB2	8514	ENSG00000069424			Kcnab2 (MGI:109239)			
chr1	6101786	6180133	1p36	1p36.31		610771	CHD5	Chromodomain helicase DNA-binding protein 5	CHD5	26038	ENSG00000116254			Chd5 (MGI:3036258)			
chr1	6185019	6199618	1p36.31	1p36.31		180474	"RPL22, EAP"	Ribosomal protein L22	RPL22	6146	ENSG00000116251	fused with AML1 in t(3;21)		Rpl22 (MGI:99262)			
chr1	6206003	6221298	1p36.31	1p36.31		616923	"RNF207, C1orf188"	RING finger protein 207	RNF207	388591	ENSG00000158286			Rnf207 (MGI:2684989)			
chr1	6221192	6235983	1p36	1p36.31		605851	ICMT	Isoprenylcysteine carboxylmethyltransferase	ICMT	23463	ENSG00000116237			Icmt (MGI:1888594)			
chr1	6244191	6245577	1p36.31	1p36.31		609971	HES3	"Hairy/enhancer of split, Drosophila, homolog of, 3"	HES3	390992	ENSG00000173673			Hes3 (MGI:104877)			
chr1	6247345	6260974	1p36.31	1p36.31		614269	GPR153	G protein-coupled receptor 153	GPR153	387509	ENSG00000158292			Gpr153 (MGI:1916157)			
chr1	6264271	6393765	1p36	1p36.31		602587	"ACOT7, BACH, LACH"	Acyl-CoA thioesterase 7	ACOT7	11332	ENSG00000097021			Acot7 (MGI:1917275)			
chr1	6415231	6419918	1p36.31	1p36.31		609970	HES2	"Hairy/enhancer of split, Drosophila, homolog of, 2"	HES2	54626	ENSG00000069812			Hes2 (MGI:1098624)			
chr1	6424775	6461366	1p36.3-p36.1	1p36.31		606351	ESPN	"Espin, mouse, homolog of"	ESPN	83715	ENSG00000187017		"Deafness, autosomal recessive 36, 609006 (3), Autosomal recessive; Deafness, neurosensory, without vestibular involvement, autosomal dominant (3)"	Espn (MGI:1861630)			
chr1	6461150	6466194	1p36.3	1p36.31		603366	"TNFRSF25, TNFRSF12, DR3, LARD"	"Tumor necrosis factor receptor superfamily, member 25"	TNFRSF25	8718	ENSG00000215788			Tnfrsf25 (MGI:1934667)			
chr1	6466091	6520060	1p36	1p36.31		611101	"PLEKHG5, KIAA0720, DSMA4, CMTRIC"	"Pleckstrin homology domain-containing protein, family G, member 5"	PLEKHG5	57449	ENSG00000171680		"Charcot-Marie-Tooth disease, recessive intermediate C, 615376 (3), Autosomal recessive; Spinal muscular atrophy, distal, autosomal recessive, 4, 611067 (3), Autosomal recessive"	Plekhg5 (MGI:2652860)			
chr1	6555277	6579756	1p36	1p36.31		606225	"TAS1R1, T1R1"	"Taste receptor type 1, member 1"	TAS1R1	80835	ENSG00000173662			Tas1r1 (MGI:1927505)			
chr1	6579990	6589279	1p36.3	1p36.31		165270	"ZBTB48, HKR3"	Zinc finger- and BTB domain-containing protein 48	ZBTB48	3104	ENSG00000204859			Zbtb48 (MGI:2140248)			
chr1	6590723	6602897	1p36.31	1p36.31		616262	"KLHL21, KIAA0469"	Kelch-like 21	KLHL21	9903	ENSG00000162413			Klhl21 (MGI:1919288)			
chr1	6624615	6635585	1p36.31	1p36.31		612532	THAP3	THAP domain-containing protein 3	THAP3	90326	ENSG00000041988			Thap3 (MGI:1917126)			
chr1	6634167	6701905	1p36.31-p36.23	1p36.31		614827	DNAJC11	"DNAJ/HSP40 homolog, subfamily C, member 11"	DNAJC11	55735	ENSG00000007923			Dnajc11 (MGI:2443386)			
chr1	6785323	7769705	1p36	1p36.31-p36.23		611501	"CAMTA1, KIAA0833, CANPMR"	Calmodulin-binding transcription activator 1	CAMTA1	23261	ENSG00000171735		"Cerebellar ataxia, nonprogressive, with mental retardation, 614756 (3), Autosomal dominant"	Camta1 (MGI:2140230)			
chr1	7100000	27600000	1p36.2-p36.1			600975	GLC3B	"Glaucoma 3, primary infantile, B"	GLC3B	2728			"Glaucoma 3, primary infantile, B, 600975 (2), Autosomal recessive"				
chr1	7100000	15900000	1p36.2			608543	SCZD12	Schizophrenia 12		619488		max lod at D1S1612	"{Schizophrenia 12}, 181500 (2), Autosomal dominant"				
chr1	7771268	7781431	1p36	1p36.23		603657	VAMP3	Vesicle-associated membrane protein 3	VAMP3	9341	ENSG00000049245			Vamp3 (MGI:1321389)			
chr1	7784284	7845180	1p36.33-p36.21	1p36.23		603427	"PER3, FASPS3"	"Period, Drosophila, homolog of, 3"	PER3	8863	ENSG00000049246	mutation identified in 1 FASPS3 family	"?Advanced sleep phase syndrome, familial, 3, 616882 (3), Autosomal dominant"	Per3 (MGI:1277134)			
chr1	7846344	7913614	1p36.23	1p36.23		604097	UTS2	Urotensin II	UTS2	10911	ENSG00000049247			Uts2 (MGI:1346329)			
chr1	7915870	7943164	1p36	1p36.23		602250	"TNFRSF9, ILA, CD137"	"Tumor necrosis factor receptor superfamily, member 9 (interleukin-activated receptor; Ly63, mouse, homolog of)"	TNFRSF9	3604	ENSG00000049249			Tnfrsf9 (MGI:1101059)			
chr1	7961653	7985281	1p36	1p36.23		602533	"DJ1, PARK7"	Oncogene DJ-1	PARK7	11315	ENSG00000116288		"Parkinson disease 7, autosomal recessive early-onset, 606324 (3), Autosomal recessive"	Park7 (MGI:2135637)			
chr1	8011718	8026332	1p36	1p36.23		608069	"MIG6, RALT"	Mitogen-inducible gene 6	ERRFI1	54206	ENSG00000116285			Errfi1 (MGI:1921405)			
chr1	8318084	8344166	1p36.2-p36.1	1p36.23		605763	"SLC45A1, DNB5, IDDNPF"	"Solute carrier family 45, member 1"	SLC45A1	50651	ENSG00000162426		"Intellectual developmental disorder with neuropsychiatric features, 617532 (3), Autosomal recessive"	Slc45a1 (MGI:2653235)			
chr1	8352403	8826225	1p36.2-p36.1	1p36.23		605226	"RERE, NEDBEH"	RE repeats-encoding gene	RERE	473	ENSG00000142599		"Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart, 616975 (3), Autosomal dominant"	Rere (MGI:2683486)			
chr1	8861001	8878685	1pter-p36.13	1p36.23		172430	"ENO1, PPH, MPB1"	"Enolase-1, alpha"	ENO1	2023	ENSG00000074800		Enolase deficiency (1)	"Eno1b,Eno1 (MGI:95393,MGI:3648653)"			
chr1	8945833	8975091	1p36.33-p36.22	1p36.23		114780	CA6	Carbonic anhydrase VI	CA6	765	ENSG00000131686			Car6 (MGI:1333786)			
chr1	8992533	9026383	1p36.2	1p36.23		610371	"SLC2A7, GLUT7"	"Solute carrier family 2 (facilitated glucose transporter), member 7"	SLC2A7	155184	ENSG00000197241			Slc2a7 (MGI:3650865)			
chr1	9036945	9072226	1p36.2	1p36.23		138230	"SLC2A5, GLUT5"	"Solute carrier family 2 (facilitated glucose transporter), member 5"	SLC2A5	6518	ENSG00000142583			Slc2a5 (MGI:1928369)			
chr1	9151667	9151776	1p36	1p36.22		611172	"MIR34A, MIRN34A"	Micro RNA 34A	MIR34A	407040							
chr1	9234766	9271336	1p36	1p36.22		138090	"H6PD, GDH, G6PDH, CORTRD1"	Hexose-6-phosphate dehydrogenase	H6PD	9563	ENSG00000049239	digenic triallelic mutations with HSD11B1	"Cortisone reductase deficiency 1, 604931 (3), Autosomal recessive"	H6pd (MGI:2140356)			
chr1	9292881	9369531	1p36.22	1p36.22		611657	"SPSB, SSB1"	SPRY domain- and SOCS box-containing 1	SPSB1	80176	ENSG00000171621			Spsb1 (MGI:1921896)			
chr1	9539468	9582772	1p36.22	1p36.22		610816	SLC25A33	"Solute carrier family 25 (mitochondrial carrier), member 33"	SLC25A33	84275	ENSG00000171612			Slc25a33 (MGI:1917806)			
chr1	9629888	9728924	1p36.2	1p36.22		602839	"PIK3CD, APDS, IMD14"	"Phosphatidylinositol 3-kinase, catalytic, 110kD, delta"	PIK3CD	5293	ENSG00000171608		"Immunodeficiency 14, 615513 (3), Autosomal dominant"	Pik3cd (MGI:1098211)			
chr1	9729020	9824525	1p36	1p36.22		611321	"CLSTN1, KIAA0911"	Calsyntenin 1	CLSTN1	22883	ENSG00000171603			Clstn1 (MGI:1929895)			
chr1	9848275	9910321	1p36.22	1p36.22		607758	"CTNNBIP1, ICAT"	"Catenin, beta-interacting protein 1"	CTNNBIP1	56998	ENSG00000178585			Ctnnbip1 (MGI:1915756)			
chr1	9922112	9943426	1p36.22	1p36.22		610458	LZIC	Leucine zipper and CTNNBIP1 domains-containing protein	LZIC	84328	ENSG00000162441			Lzic (MGI:1916401)			
chr1	9942922	9996883	1p36.22	1p36.22		608700	"NMNAT1, NMNAT, PNAT1, LCA9"	Nicotinamide nucleotide adenylyltransferase 1	NMNAT1	64802	ENSG00000173614		"Leber congenital amaurosis 9, 608553 (3), Autosomal recessive"	Nmnat1 (MGI:1913704)			
chr1	10032957	10181238	1p36.3	1p36.22		613565	"UBE4B, UFD2A, KIAA0684"	Ubiquitination factor E4B	UBE4B	10277	ENSG00000130939			Ube4b (MGI:1927086)			
chr1	10210705	10381602	1p36.2	1p36.22		605995	"KIF1B, CMT2A, CMT2A1, NBLST1"	Kinesin family member 1B	KIF1B	23095	ENSG00000054523	mutation identified in 1 CMT2A1 family	"?Charcot-Marie-Tooth disease, type 2A1, 118210 (3), Autosomal dominant; {Neuroblastoma, susceptibility to, 1}, 256700 (3), Autosomal dominant, Isolated cases; Pheochromocytoma, 171300 (3), Autosomal dominant"	Kif1b (MGI:108426)			
chr1	10398991	10420510	1p36.2-p36.13	1p36.22		172200	PGD	6-phosphogluconate dehydrogenase	PGD	5226	ENSG00000142657			Pgd (MGI:97553)			
chr1	10430101	10442814	1p36.22	1p36.22		609130	APITD1	"Apoptosis-inducing, TAF9-like domain 1"	CENPS	378708	ENSG00000175279			Cenps (MGI:1917178)			
chr1	10449718	10452002	1p36	1p36.22		602784	CORT	Cortistatin	CORT	1325	ENSG00000241563			Cort (MGI:109538)			
chr1	10460530	10472555	1p36.3-p36.2	1p36.22		601882	"DFFA, DFF1"	"DNA fragmentation factor, 45kD, alpha subunit"	DFFA	1676	ENSG00000160049			Dffa (MGI:1196227)			
chr1	10474945	10630757	1p36.2	1p36.22		601791	"PEX14, PBD13A"	Peroxisome biogenesis factor 14	PEX14	5195	ENSG00000142655		"Peroxisome biogenesis disorder 13A (Zellweger), 614887 (3), Autosomal recessive"	Pex14 (MGI:1927868)			
chr1	10636603	10796675	1p36.22	1p36.22		609895	"CASZ1, SRG"	Castor zinc finger protein 1	CASZ1	54897	ENSG00000130940			Casz1 (MGI:1196251)			
chr1	11012621	11030527	1p36.2	1p36.22		605078	"TARDBP, TDP43, ALS10"	TAR DNA-binding protein	TARDBP	23435	ENSG00000120948	"pseudogenes on 2, 6, 8, 13, 20"	"Amyotrophic lateral sclerosis 10, with or without FTD, 612069 (3), Autosomal dominant; Frontotemporal lobar degeneration, TARDBP-related, 612069 (3), Autosomal dominant"	Tardbp (MGI:2387629)			
chr1	11026522	11047238	1p36.3-p36.2	1p36.22		605102	MASP2	Mannan-binding lectin serine protease 2	MASP2	10747	ENSG00000009724		"MASP2 deficiency, 613791 (3), Autosomal recessive"	Masp2 (MGI:1330832)			
chr1	11054591	11060052	1p36-p22	1p36.22		182891	"SRM, SPS1"	Spermidine synthase-1	SRM	6723	ENSG00000116649	?pseudogene on 3p14-q21		Srm (MGI:102690)			
chr1	11066612	11099909	1p36.22	1p36.22		605960	"EXOSC10, PMSCL2"	Exosome component 10	EXOSC10	5394	ENSG00000171824			Exosc10 (MGI:1355322)			
chr1	11106530	11273496	1p36.2	1p36.22		601231	"MTOR, FRAP1, SKS"	Mechanistic target of rapamycin	MTOR	2475	ENSG00000198793		"Focal cortical dysplasia, type II, somatic, 607341 (3); Smith-Kingsmore syndrome, 616638 (3), Autosomal dominant"	Mtor (MGI:1928394)			
chr1	11273197	11299571	1p36.3	1p36.22		611632	"UBIAD1, TERE1, SCCD"	UbiA prenyltransferase domain-containing protein 1	UBIAD1	29914	ENSG00000120942		"Corneal dystrophy, Schnyder type, 121800 (3), Autosomal dominant"	Ubiad1 (MGI:1918957)			
chr1	11479154	11537582	1p36.22	1p36.22		611251	"PTCHD2, DISP3, KIAA1337"	Patched domain-containing protein 2	DISP3	57540	ENSG00000204624			Disp3 (MGI:2444403)			
chr1	11648360	11654830	1p36	1p36.22		607112	"FBXO2, FBX2, FBG1, NFB42"	F-box only protein 2	FBXO2	26232	ENSG00000116661			Fbxo2 (MGI:2446216)			
chr1	11654374	11663326	1p36.21	1p36.22		609111	"FBXO44, FBX44, FBX6A, FBG3"	F-box only protein 44	FBXO44	93611	ENSG00000132879			Fbxo44 (MGI:1354744)			
chr1	11664092	11674353	1p36.23	1p36.22		605647	"FBXO6, FBX6, FBG2"	F-box only protein 6	FBXO6	26270	ENSG00000116663			Fbxo6 (MGI:1354743)			
chr1	11674479	11691620	1p36	1p36.22		604094	"MAD2L2, MAD2B, FANCV"	"Mitotic arrest-deficient 2, S. cerevisiae, homolog-like 2"	MAD2L2	10459	ENSG00000116670	mutation identified in 1 FANCV patient; pseudogene on 14q21-q23	"?Fanconi anemia, complementation group V, 617243 (3), Autosomal recessive"	Mad2l2 (MGI:1919140)			
chr1	11686634	11721765	1p36.22	1p36.22		612682	"DRAXIN, C1orf187"	Dorsal repulsive axon guidance protein	DRAXIN	374946	ENSG00000162490			Draxin (MGI:1917683)			
chr1	11785729	11806102	1p36.3	1p36.22		607093	MTHFR	Methylenetetrahydrofolate reductase	MTHFR	4524	ENSG00000177000		"Homocystinuria due to MTHFR deficiency, 236250 (3), Autosomal recessive; {Neural tube defects, susceptibility to}, 601634 (3), Autosomal recessive; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant; {Thromboembolism, susceptibility to}, 188050 (3), Autosomal dominant; {Vascular disease, susceptibility to} (3)"	Mthfr (MGI:106639)			
chr1	11806095	11843143	1p36	1p36.22		602726	CLCN6	Chloride channel 6	CLCN6	1185	ENSG00000011021			Clcn6 (MGI:1347049)			
chr1	11845708	11847782	1p36.2	1p36.22		108780	"NPPA, PND, ANP, ATFB6, ATRST2"	Natriuretic peptide precursor A	NPPA	4878	ENSG00000175206		"Atrial fibrillation, familial, 6, 612201 (3), Autosomal dominant; Atrial standstill 2, 615745 (3), Autosomal recessive"	Nppa (MGI:97367)			
chr1	11857463	11858934	1p36.2	1p36.22		600295	"NPPB, BNP"	Natriuretic peptide precursor B	NPPB	4879	ENSG00000120937						
chr1	11934666	11975541	1p36.3-p36.2	1p36.22		153454	"PLOD1, LH1, LLH, EDSKCL1"	"Procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase)"	PLOD1	5351	ENSG00000083444		"Ehlers-Danlos syndrome, kyphoscoliotic type, 1, 225400 (3), Autosomal recessive"	Plod1 (MGI:99907)			
chr1	11980180	12013514	1p36.2	1p36.22		608507	"MFN2, KIAA0214, CMT2A2A, HMSN6A, CMT2A2B"	Mitofusin 2	MFN2	9927	ENSG00000116688		"Charcot-Marie-Tooth disease, axonal, type 2A2A, 609260 (3), Autosomal dominant; Charcot-Marie-Tooth disease, axonal, type 2A2B, 617087 (3), Autosomal recessive; Hereditary motor and sensory neuropathy VIA, 601152 (3), Autosomal dominant"	Mfn2 (MGI:2442230)			
chr1	12063316	12144212	1p36	1p36.22		153243	"TNFRSF8, CD30, D1S166E"	"Tumor necrosis factor receptor superfamily, member 8 (CD30 antigen; Ki-1 antigen)"	TNFRSF8	943	ENSG00000120949			Tnfrsf8 (MGI:99908)			
chr1	12166947	12209221	1p36.3-p36.2	1p36.22		191191	"TNFRSF1B, TNFR2, TNFBR"	"Tumor necrosis factor receptor superfamily, member 1B"	TNFRSF1B	7133	ENSG00000028137			Tnfrsf1b (MGI:1314883)			
chr1	12500000	15900000	1p36.21			609918	GBD2	Gallbladder disease 2	GBD2	100048905		between D1S1597 and D1S47	"Gallbladder disease 2, 609918 (2)"				
chr1	12567909	12617730	1p36.1	1p36.21		612830	"DHRS3, RETSDR1"	"Short-chain dehydrogenase/reductase family, member 3"	DHRS3	9249	ENSG00000162496			Dhrs3 (MGI:1315215)			
chr1	13474976	13513746	1p36.21	1p36.21		615212	LRRC38	Leucine-rich repeat-containing protein 38	LRRC38	126755	ENSG00000162494			Lrrc38 (MGI:2442845)			
chr1	13583756	13617956	1p36.21	1p36.21		608863	"PDPN, TI1A, T1A2, GP36, OTS8, AGGRUS"	Podoplanin	PDPN	10630	ENSG00000162493			Pdpn (MGI:103098)			
chr1	13698873	13825078	1p36	1p36.21		601196	"PRDM2, RIZ"	PR domain-containing protein 2 (retinoblastoma protein-binding zinc-finger protein RIZ)	PRDM2	7799	ENSG00000116731			Prdm2 (MGI:107628)			
chr1	15409894	15430342	1p36.21	1p36.21		616450	"EFHD2, SWS1"	"EF-hand domain family, member D2"	EFHD2	79180	ENSG00000142634			Efhd2 (MGI:106504)			
chr1	15438441	15449246	1p36.21	1p36.21		601405	"CTRC, CLCR"	Chymotrypsin	CTRC	11330	ENSG00000162438		"{Pancreatitis, chronic, susceptibility to}, 167800 (3), Autosomal dominant"	Ctrc (MGI:1923951)			
chr1	15456727	15472090	1p36.2	1p36.21		609443	"CELA2A, ELA2A"	"Chymotrypsin-like elastase family, member 2A"	CELA2A	63036	ENSG00000142615			Cela2a (MGI:95316)			
chr1	15476100	15491399	1p36.2	1p36.21		609444	"CELA2B, ELA2B"	"Chymotrypsin-like elastase family, member 2B"	CELA2B	51032	ENSG00000215704						
chr1	15491400	15524911	1p36.3-p36.1	1p36.21		602234	"CASP9, APAF3"	"Caspase 9, apoptosis-related cysteine protease"	CASP9	842	ENSG00000132906			Casp9 (MGI:1277950)			
chr1	15571698	15585109	1p36.21	1p36.21		617887	"AGMAT, AUH"	Agmatinase	AGMAT	79814	ENSG00000116771			Agmat (MGI:1923236)			
chr1	15659712	15662029	1p36.1	1p36.21		601966	"RSC1A1, RS1"	"Regulatory solute carrier protein, family 1, member 1"	RSC1A1	6248	ENSG00000215695			Rsc1a1 (MGI:3526447)			
chr1	15681505	15734768	1p36.21	1p36.21		609613	"PLEKHM2, SKIP, KIAA0842"	"Pleckstrin homology domain-containing protein, family M, member 2"	PLEKHM2	23207	ENSG00000116786			Plekhm2 (MGI:1916832)			
chr1	15735087	15741391	1p36.21	1p36.21		610817	SLC25A34	"Solute carrier family 25, member 34"	SLC25A34	284723	ENSG00000162461			Slc25a34 (MGI:2686215)			
chr1	15756169	15786593	1p36.13	1p36.21		607747	"FBLP1, MIGFILIN"	Filamin-binding LIM protein 1	FBLIM1	54751	ENSG00000162458			Fblim1 (MGI:1921452)			
chr1	15847863	15940454	1p36.13	1p36.21-p36.13		613484	"SPEN, MINT, SHARP, HIAA0929"	"SPEN, Drosophila, homolog of"	SPEN	23013	ENSG00000065526			Spen (MGI:1891706)			
chr1	15900000	39600000	1p36.13-p34.3			609122	ANIB3	"Aneurysm, intracranial berry, 3"	ANIB3	497657			"Aneurysm, intracranial berry, 3, 609122 (2), Autosomal dominant"				
chr1	15900000	39600000	1p36.13-p34.3			616055	EA8	"Episodic ataxia, type 8"		104326187		between rs2743201 and rs215791	"Episodic ataxia, type 8, 616055 (2), Autosomal dominant"				
chr1	15900000	34300000	1p36.1-p35			601201	MEMO1	Methylation modifier for class I HLA		7795							
chr1	15939932	15976131	1p36.2-p36.1	1p36.13		604084	"ZBTB17, ZNF151, MIZ1"	Zinc finger- and BTB domain-containing protein 17	ZBTB17	7709	ENSG00000116809			Zbtb17 (MGI:107410)			
chr1	16014027	16019593	1p36.23-p34.3	1p36.13		610692	"HSPB7, CVHSP"	Heat-shock 27kD protein 7	HSPB7	27129	ENSG00000173641			Hspb7 (MGI:1352494)			
chr1	16021990	16034049	1p36	1p36.13		602024	CLCNKA	"Chloride channel, kidney, A"	CLCNKA	1187	ENSG00000186510	11kb from CLCNKB; simultaneous mutation in CLCNKA and CLCNKB	"Bartter syndrome, type 4b, digenic, 613090 (3), Digenic recessive"	Clcnkb (MGI:1930643)			
chr1	16043735	16057325	1p36	1p36.13		602023	CLCNKB	"Chloride channel, kidney, B"	CLCNKB	1188	ENSG00000184908	unequal crossingover with CLCNKA	"Bartter syndrome, type 3, 607364 (3), Autosomal recessive; Bartter syndrome, type 4b, digenic, 613090 (3), Digenic recessive"	Clcnka (MGI:1329026)			
chr1	16124336	16156108	1p36.1	1p36.13		176946	"EPHA2, ECK, CTPP1, CTPA, ARCC2, CTRCT6"	Ephrin receptor EphA2	EPHA2	1969	ENSG00000142627		"Cataract 6, multiple types, 116600 (3), Autosomal dominant"	Epha2 (MGI:95278)			
chr1	16197853	16212699	1p36.13	1p36.13		612496	"ARHGEF19, WGEF"	RHO guanine nucleotide exchange factor 19	ARHGEF19	128272	ENSG00000142632			Arhgef19 (MGI:1925912)			
chr1	16246839	16352490	1p36.23-p36.11	1p36.13		609109	"FBXO42, FBX42, KIAA1332"	F-box only protein 42	FBXO42	54455	ENSG00000037637			Fbxo42 (MGI:1924992)			
chr1	16440671	16460089	1p36.13	1p36.13		611624	NECAP2	NECAP endocytosis-associated protein 2	NECAP2	55707	ENSG00000157191			Necap2 (MGI:1913397)			
chr1	16545938	16546008	Chr.16	1p36.13		189911	"TRNAG1, TRG1"	tRNA glycine-1		7195							
chr1	16562426	16613604	1p36.2	1p36.13		610501	"NBPF1, KIAA1693"	"Neuroblastoma breakpoint family, member 1"	NBPF1	55672		pseudogenes on 3 and 5					
chr1	16740515	16740678	1p36.3	1p36.13		180680	"RNU1A, RNU1"	"RNA, U1A small nuclear"	RNU1-4	6060		?same as A12M2					
chr1	16872582	16872653	1p36	1p36.13		180640	"TRNAE1, TRNE, TRE"	tRNA glutamic acid	TRE-TTC3-1	7193							
chr1	16914081	16972978	1p36.11	1p36.13		615776	"CROCC, ROOTLETIN, KIAA0445"	Ciliary rootlet coiled-coil protein	CROCC	9696	ENSG00000058453			Crocc (MGI:3529431)			
chr1	16974501	16981585	1p36.1-p35	1p36.13		156790	"MFAP2, MAGP, MAGP1"	Microfibrillar-associated protein-2	MFAP2	4237	ENSG00000117122			Mfap2 (MGI:99559)			
chr1	16985957	17011971	1p36	1p36.13		610513	"ATP13A2, PARK9, KRPPD, SPG78"	"ATPase, type 13A2"	ATP13A2	23400	ENSG00000159363	mutation identified in 1 family with CLN12	"Kufor-Rakeb syndrome, 606693 (3), Autosomal recessive; Spastic paraplegia 78, autosomal recessive, 617225 (3), Autosomal recessive"	Atp13a2 (MGI:1922022)			
chr1	17018721	17054169	1p36.1-p35	1p36.13		185470	"SDHB, SDH2, SDHIP, PGL4, CWS2"	"Succinate dehydrogenase complex, subunit B, iron sulfur (Ip)"	SDHB	6390	ENSG00000117118	1 of 2 polypeptides	"Cowden syndrome 2, 612359 (3), Autosomal dominant; Gastrointestinal stromal tumor, 606764 (3), Autosomal dominant, Isolated cases; Paraganglioma and gastric stromal sarcoma, 606864 (3); Paragangliomas 4, 115310 (3), Autosomal dominant; Pheochromocytoma, 171300 (3), Autosomal dominant"	Sdhb (MGI:1914930)			
chr1	17066760	17119452	1p36.13	1p36.13		607935	PADI2	"Peptidylarginine deiminase, type II"	PADI2	11240	ENSG00000117115			Padi2 (MGI:1338892)			
chr1	17205124	17246005	1p36.13	1p36.13		607934	PADI1	"Peptidylarginine deiminase, type I"	PADI1	29943	ENSG00000142623			Padi1 (MGI:1338893)			
chr1	17249078	17284232	1p36.13	1p36.13		606755	"PADI3, UHS1"	"Peptidylarginine deiminase, type III"	PADI3	51702	ENSG00000142619		"Uncombable hair syndrome, 191480 (3), Autosomal recessive"	Padi3 (MGI:1338891)			
chr1	17308194	17364003	1p36.13	1p36.13		605347	"PADI4, PADI5, PAD"	"Peptidylarginine deiminase, type IV"	PADI4	23569	ENSG00000159339		"{Rheumatoid arthritis, susceptibility to}, 180300 (3)"	Padi4 (MGI:1338898)			
chr1	17372195	17401698	1p36.13	1p36.13		610363	"PADI6, PREMBL2"	"Peptidylarginine deiminase, type VI"	PADI6	353238	ENSG00000276747		"Preimplantation embryonic lethality 2, 617234 (3), Autosomal recessive"	Padi6 (MGI:2655198)			
chr1	17513441	17697874	1p36.13	1p36.13		612494	"ARHGEF10L, GRINCHGEF, KIAA1626"	RHO guanine nucleotide exchange factor 10-like protein	ARHGEF10L	55160	ENSG00000074964			Arhgef10l (MGI:1920004)			
chr1	18631005	18748865	1p36.2-p36.12	1p36.13		167410	"PAX7, RMS2"	Paired box homeotic gene-7	PAX7	5081	ENSG00000009709	fused with FKHR in rhabdomyosarcoma	"Rhabdomyosarcoma 2, alveolar, 268220 (3), Autosomal recessive"	Pax7 (MGI:97491)			
chr1	18839598	18859660	1p36	1p36.13		606226	"TAS1R2, T1R2"	"Taste receptor type 1, member 2"	TAS1R2	80834	ENSG00000179002			Tas1r2 (MGI:1933546)			
chr1	18871429	18902798	1p36	1p36.13		606811	"ALDH4A1, ALDH4, P5CDH"	"Aldehyde dehydrogenase 4 family, member A1 (delta-1-pyrroline 5-carboxylate dehydrogenase)"	ALDH4A1	8659	ENSG00000159423		"Hyperprolinemia, type II, 239510 (3), Autosomal recessive"	Aldh4a1 (MGI:2443883)			
chr1	19074505	19214331	1p36.13	1p36.13		609890	"UBR4, ZUBR1, RBAF600, KIAA1307"	Ubiquitin protein ligase E3 component n-recognin 4	UBR4	23352	ENSG00000127481			Ubr4 (MGI:1916366)			
chr1	19215663	19251558	1p36.13	1p36.13		616846	"EMC1, KIAA0090, CAVIPMR"	"Endoplasmic reticulum membrane protein complex, subunit 1"	EMC1	23065	ENSG00000127463		"Cerebellar atrophy, visual impairment, and psychomotor retardation, 616875 (3), Autosomal recessive"	Emc1 (MGI:2443696)			
chr1	19259319	19274167	1p36.13	1p36.13		608478	"AKR7A4, AFAR3"	"Aldo-keto reductase family 7, member A4"	AKR7L	246181							
chr1	19274228	19289361	1p36.13	1p36.13		608477	"AKR7A3, AFAR2"	"Aldo-keto reductase family 7, member A3"	AKR7A3	22977	ENSG00000162482						
chr1	19302707	19312145	1p36.13	1p36.13		603418	"AKR7A2, AKR7, AFAR"	"Aldo-keto reductase family 7, member A2"	AKR7A2	8574	ENSG00000053371	pseudogenes on Xq25 and 1p12		Akr7a5 (MGI:107796)			
chr1	19312245	19332610	1p36.13	1p36.13		614760	PQLC2	PQ loop repeat-containing protein 2	PQLC2	54896	ENSG00000040487			Pqlc2 (MGI:2384837)			
chr1	19338772	19485640	1p36.1	1p36.13		601572	"CAPZB, CAPPB"	"Capping protein (actin filament) muscle Z-line, beta"	CAPZB	832	ENSG00000077549			Capzb (MGI:104652)			
chr1	19596976	19629820	1p36.13	1p36.13		616574	"MINOS1, MIO10, MIC10"	Mitochondrial inner membrane organizing system protein 1	MINOS1	440574	ENSG00000173436			Minos1 (MGI:1913628)			
chr1	19643228	19658455	1p36.13-p36.11	1p36.13		600613	"D1S1733E, DAN"	Differential-screening-selected gene aberrant in neuroblastoma	NBL1	4681	ENSG00000158747	aberrant in some neuroblastomas		Nbl1 (MGI:104591)			
chr1	19665286	19680965	1p36-p35	1p36.13		601109	HTR6	5-hydroxytryptamine (serotonin) receptor-6	HTR6	3362	ENSG00000158748			Htr6 (MGI:1196627)			
chr1	19814028	19815277	1p36.13	1p36.13		617163	RNF186	Ring finger protein 186	RNF186	54546	ENSG00000178828			Rnf186 (MGI:1914075)			
chr1	19881707	19912944	1p36.13	1p36.13		611758	"OTUD3, KIAA0459"	OTU domain-containing protein 3	OTUD3	23252	ENSG00000169914			Otud3 (MGI:1920412)			
chr1	19975430	19980438	1p35	1p36.13		172411	"PLA2G2A, PLA2B, PLA2L, MOM1"	"Phospholipase A2, group IIA, platelets, synovial fluid"	PLA2G2A	5320	ENSG00000188257		"{Colorectal cancer}, 114500 (3), Autosomal dominant"				
chr1	20028348	20091900	1p36-p34	1p36.13		601192	"PLA2G5, FRFB"	"Phospholipase A2, group V"	PLA2G5	5322	ENSG00000127472		"[Fleck retina, familial benign], 228980 (3), Autosomal recessive"	Pla2g5 (MGI:101899)			
chr1	20100000	23600000	1p36.12			612957	B6QTL1	Vitamin B6 plasma level QTL 1		100302718		associated with rs4654748	"{Vitamin B6 plasma level QTL 1}, 612957 (2)"				
chr1	20100000	34300000	1p36.12-p35.1			612627	"BFIS4, BFIC4"	"Seizures, benign familial infantile, 4"		100271922		between D1S2864 and D1S2830	"Seizures, benign familial infantile, 4, 612627 (2)"				
chr1	20112649	20119565	1p36.12	1p36.12		605630	"PLA2G2D, SPLASH"	"Phospholipase A2, group IID"	PLA2G2D	26279	ENSG00000117215			Pla2g2d (MGI:1341796)			
chr1	20139325	20150385	1p35	1p36.12		616793	PLA2G2F	"Phospholipase A2, group IIf"	PLA2G2F	64600	ENSG00000158786			Pla2g2f (MGI:1349661)			
chr1	20183006	20196047	1p36.12	1p36.12		616783	UBXN10	UBX domain protein 10	UBXN10	127733	ENSG00000162543			Ubxn10 (MGI:2443123)			
chr1	20482390	20486234	1p36.12	1p36.12		614986	CAMK2N1	Calcium/calmodulin-dependent protein kinase II inhibitor 1	CAMK2N1	55450	ENSG00000162545			Camk2n1 (MGI:1913509)			
chr1	20499447	20508482	1p36.12	1p36.12		612037	"MUL1, MULAN, C1orf166"	Mitochondrial ubiquitin ligase activator of NFKB1	MUL1	79594	ENSG00000090432			Mul1 (MGI:1915600)			
chr1	20588950	20618907	1p36.2-p35	1p36.12		123920	CDA	Cytidine deaminase	CDA	978	ENSG00000158825			Cda (MGI:1919519)			
chr1	20633454	20651510	1p36	1p36.12		608309	"PINK1, PARK6"	PTEN-induced putative kinase 1	PINK1	65018	ENSG00000158828		"Parkinson disease 6, early onset, 605909 (3), Autosomal recessive"	Pink1 (MGI:1916193)			
chr1	20651766	20661543	1p36.1	1p36.12		602202	"DDOST, OST, OST48, CDG1R"	Dolichyl-diphosphooligosaccharide-protein glycosyltransferase	DDOST	1650	ENSG00000244038	mutation (cmpd het) identified in 1 CDG1R patient	"?Congenital disorder of glycosylation, type Ir, 614507 (3), Autosomal recessive"	Ddost (MGI:1194508)			
chr1	20664013	20718016	1p36.12	1p36.12		605037	"KIF17, KIAA1405"	Kinesin family member 17	KIF17	57576	ENSG00000117245			Kif17 (MGI:1098229)			
chr1	20742676	20787807	1p36.12	1p36.12		616072	"HP1BP3, HP1BP74"	Heterochromatin protein 1-binding protein 3	HP1BP3	50809	ENSG00000127483			Hp1bp3 (MGI:109369)			
chr1	20806291	21176887	1p36.12	1p36.12		603929	"EIF4G3, EIF4GII"	"Eukaryotic translation initiation factor 4-gamma, 3"	EIF4G3	8672	ENSG00000075151			Eif4g3 (MGI:1923935)			
chr1	21217246	21345540	1p36.1	1p36.12		600423	ECE1	Endothelin converting enzyme 1	ECE1	1889	ENSG00000117298	mutation identified in 1 HCAD patient	"?Hirschsprung disease, cardiac defects, and autonomic dysfunction, 613870 (3), Autosomal dominant; {Hypertension, essential, susceptibility to}, 145500 (3), Multifactorial"	Ece1 (MGI:1101357)			
chr1	21436774	21484899	1p36.2	1p36.12		612992	NBPF3	"Neuroblastoma breakpoint family, member 3"	NBPF3	84224	ENSG00000142794						
chr1	21508981	21578411	1p36.1-p34	1p36.12		171760	"ALPL, HOPS, TNSALP"	"Alkaline phosphatase, liver/bone/kidney"	ALPL	249	ENSG00000162551		"Hypophosphatasia, adult, 146300 (3), Autosomal recessive, Autosomal dominant; Hypophosphatasia, childhood, 241510 (3), Autosomal recessive; Hypophosphatasia, infantile, 241500 (3), Autosomal recessive; Odontohypophosphatasia, 146300 (3), Autosomal recessive, Autosomal dominant"	Alpl (MGI:87983)			
chr1	21596220	21669443	1p36.1-p35	1p36.12		600278	RAP1GA1	"RAP1, GTPase activating protein 1"	RAP1GAP	5909	ENSG00000076864			Rap1gap (MGI:109338)			
chr1	21678578	21784145	1p36	1p36.12		617445	"USP48, USP31"	Ubiquitin-specific peptidase 48	USP48	84196	ENSG00000090686			Usp48 (MGI:2158502)			
chr1	21822231	21937296	1p36.1	1p36.12		142461	"HSPG2, PLC, SJS, SJA, SJS1"	Heparan sulfate proteoglycan of basement membrane (perlecan)	HSPG2	3339	ENSG00000142798		"Dyssegmental dysplasia, Silverman-Handmaker type, 224410 (3), Autosomal recessive; Schwartz-Jampel syndrome, type 1, 255800 (3), Autosomal recessive"	Hspg2 (MGI:96257)			
chr1	22052626	22092942	1p36.1	1p36.12		116952	"CDC42, TKS"	"Cell division cycle 42 (GTP-binding protein, 25kD)"	CDC42	998	ENSG00000070831		"Takenouchi-Kosaki syndrome, 616737 (3)"				
chr1	22117304	22143980	1p35	1p36.12		603490	"WNT4, SERKAL"	"Wingless-type MMTV integration site family, member 4"	WNT4	54361	ENSG00000162552	mutation identified in 1 SERKAL family	"Mullerian aplasia and hyperandrogenism, 158330 (3), Autosomal dominant; ?SERKAL syndrome, 611812 (3), Autosomal recessive"	Wnt4 (MGI:98957)			
chr1	22428837	22531156	1p36	1p36.12		612106	"ZBTB40, KIAA0478"	Zinc finger- and BTB domain-containing protein 40	ZBTB40	9923	ENSG00000184677			Zbtb40 (MGI:2682254)			
chr1	22563501	22603593	1p36.12	1p36.12		176945	"EPHA8, EEK, HEK3"	Ephrin receptor EphA8 (eph- and elk-related kinase)	EPHA8	2046	ENSG00000070886			Epha8 (MGI:109378)			
chr1	22636505	22639681	1p36.3-p34.1	1p36.12		120550	C1QA	"Complement component 1, q subcomponent, A chain"	C1QA	712	ENSG00000173372		"C1q deficiency, 613652 (3), Autosomal recessive"	C1qa (MGI:88223)			
chr1	22643616	22648110	1p36.3-p34.1	1p36.12		120575	"C1QC, C1QG"	"Complement component 1, q subcomponent, C chain"	C1QC	714	ENSG00000159189		"C1q deficiency, 613652 (3), Autosomal recessive"	C1qc (MGI:88225)			
chr1	22652980	22661636	1p36.3-p34.1	1p36.12		120570	C1QB	"Complement component 1, q subcomponent, B chain"	C1QB	713	ENSG00000173369		"C1q deficiency, 613652 (3), Autosomal recessive"	C1qb (MGI:88224)			
chr1	22710769	22921499	1p36.1-p35	1p36.12		600997	"EPHB2, EPHT3, DRT, ERK, PCBC, CAPB"	eph tyrosine kinase 3 (ephrin receptor EphB2)	EPHB2	2048	ENSG00000133216		"{Prostate cancer/brain cancer susceptibility, somatic}, 603688 (3)"	Ephb2 (MGI:99611)			
chr1	23019442	23083690	1p36.12	1p36.12		609132	"KDM1A, LSD1, AOF2, BHC110, KIAA0601, CPRF"	Lysine-specific demethylase 1A	KDM1A	23028	ENSG00000004487		"Cleft palate, psychomotor retardation, and distinctive facial features, 616728 (3), Autosomal dominant"	Kdm1a (MGI:1196256)			
chr1	23084022	23177807	1p36	1p36.12		601422	LUZP1	Leucine zipper protein 1	LUZP1	7798	ENSG00000169641			Luzp1 (MGI:107629)			
chr1	23191894	23194728	1p36.3-p34.3	1p36.12		182133	HTR1D	5-hydroxytryptamine (serotonin) receptor-1D	HTR1D	3352	ENSG00000179546			Htr1d (MGI:96276)			
chr1	23304687	23344363	1p36.11	1p36.12		607201	"HNRPR, HNRNPR"	Heterogeneous nuclear ribonucleoprotein R	HNRNPR	10236	ENSG00000125944			Hnrnpr (MGI:1891692)			
chr1	23359447	23369863	1p36	1p36.12		611703	"ZNF436, KIAA1710"	Zinc finger protein 436	ZNF436	80818	ENSG00000125945			Zfp46 (MGI:99192)			
chr1	23380908	23424778	1p36.12	1p36.12		604128	TCEA3	"Transcription elongation factor A, 3"	TCEA3	6920	ENSG00000204219			Tcea3 (MGI:1196908)			
chr1	23428562	23484630	1p36.13	1p36.12		616594	"ASAP3, UPLC1, CENTB6, DDEFL1, ACAP4"	"ARF GTPase-activating protein with SH3 domain, ankyrin repeat, and PH domain 3"	ASAP3	55616	ENSG00000088280			Asap3 (MGI:2684986)			
chr1	23505695	23531249	1p36	1p36.12		600426	E2F2	E2F transcription factor 2	E2F2	1870	ENSG00000007968			E2f2 (MGI:1096341)			
chr1	23557929	23559793	1p36.13-p36.12	1p36.12		600277	ID3	"Inhibitor of DNA binding 3, dominant negative, helix-loop-helix protein"	ID3	3399	ENSG00000117318			Id3 (MGI:96398)			
chr1	23626952	23640567	1p36.1	1p36.11		607305	MDS2	Myelodysplasia syndrome gene 2	MDS2	259283		fused with ETV6 in myelodysplastic syndrome					
chr1	23691778	23696834	1p36.1-p35	1p36.11		604175	"RPL11, DBA7"	Ribosomal protein L11	RPL11	6135	ENSG00000142676		"Diamond-Blackfan anemia 7, 612562 (3), Autosomal dominant"	Rpl11 (MGI:1914275)			
chr1	23743365	23762058	1p36.1	1p36.11		600786	TCEB3	"Transcription elongation factor B (SIII), polypeptide 3 (110kD, elongin A)"	ELOA	6924	ENSG00000011007			Eloa (MGI:1351315)			
chr1	23790788	23795538	1p36.11	1p36.11		616143	"LYPLA2, APT2"	Lysophospholipase II	LYPLA2	11313	ENSG00000011009			Lypla2 (MGI:1347000)			
chr1	23795598	23800803	1p36-p35	1p36.11		606953	GALE	UDP galactose-4-epimerase	GALE	2582	ENSG00000117308		"Galactose epimerase deficiency, 230350 (3), Autosomal recessive"	Gale (MGI:1921496)			
chr1	23801876	23825458	1pter-p33	1p36.11		613898	HMGCL	3-hydroxy-3-methylglutaryl-Coenzyme A lyase	HMGCL	3155	ENSG00000117305		"HMG-CoA lyase deficiency, 246450 (3), Autosomal recessive"	Hmgcl (MGI:96158)			
chr1	23845076	23868368	1p34	1p36.11		612280	FUCA1	"Fucosidase, alpha-L- 1, tissue"	FUCA1	2517	ENSG00000179163	8cM distal to RH; pseudogene on 2q31-q32	"Fucosidosis, 230000 (3), Autosomal recessive"	Fuca1 (MGI:95593)			
chr1	23873074	23913326	1p36	1p36.11		605051	"CNR2, CB2, CX5"	Cannabinoid receptor 2	CNR2	1269	ENSG00000188822			Cnr2 (MGI:104650)			
chr1	23959163	23963461	1p36.11	1p36.11		611882	PNRC2	Proline-rich nuclear receptor coactivator 2	PNRC2	55629	ENSG00000189266			Pnrc2 (MGI:106512)			
chr1	23964346	23980462	1p36.1	1p36.11		605221	"SRSF10, FUSIP1, TASR, TASR1, TASR2"	"Splicine factor, serine/arginine-rich, 10"	SRSF10	10772	ENSG00000188529	"pseudogenes on chr. 9, 12, 20"		Srsf10 (MGI:1333805)			
chr1	24056040	24112174	1p36.11	1p36.11		616832	MYOM3	Myomesin 3	MYOM3	127294	ENSG00000142661			Myom3 (MGI:2685280)			
chr1	24154155	24187294	1p36.11	1p36.11		607404	"IFNLR1, IL28RA"	"Interferon, lambda receptor 1"	IFNLR1	163702	ENSG00000185436			Ifnlr1 (MGI:2429859)			
chr1	24319321	24364481	1p36.11	1p36.11		608317	"GRHL3, SOM, TFCP2L4, VWS2"	Grainyhead-like 3	GRHL3	57822	ENSG00000158055		"Van der Woude syndrome 2, 606713 (3), Autosomal dominant"	Grhl3 (MGI:2655333)			
chr1	24356998	24415532	1p36.11	1p36.11		615826	"STPG1, MAPO2, C1orf201"	Sperm-tail PG-rich repeat-containing protein 1	STPG1	90529	ENSG00000001460			Stpg1 (MGI:1926056)			
chr1	24502350	24537019	1p35.2-p33	1p36.11		605860	"RCAN3, DSCR1L2, MCIP3"	Regulator of calcineurin 3	RCAN3	11123	ENSG00000117602			Rcan3 (MGI:1858220)			
chr1	24643102	24673280	1p36.11	1p36.11		605975	"SRRM1, SRM160"	"Serine/arginine repetitive matrix 1 (ser/arg-related nuclear matrix protein, 160kD)"	SRRM1	10250	ENSG00000133226						
chr1	24899510	24965157	1p36	1p36.11		600210	"RUNX3, CBFA3, PEBP2A3, AML2"	Runt-related transcription factor 3	RUNX3	864	ENSG00000020633			Runx3 (MGI:102672)			
chr1	25222275	25232521	1p36.11	1p36.11		607090	"SYF2, P29"	"SYF2 RNA splicing factor, S. cerevisiae, homolog of"	SYF2	25949	ENSG00000117614			Syf2 (MGI:1915842)			
chr1	25272392	25330444	1p36.2-p34	1p36.11		111680	RHD	Rhesus system D polypeptide	RHD	6007	ENSG00000187010		[Rh-negative blood type] (3)	Rhd (MGI:1202882)			
chr1	25338297	25362360	1p36.11	1p36.11		605348	"TMEM50A, SMP1"	Transmembrane protein 50A	TMEM50A	23585	ENSG00000183726	between RHD and RHCE		Tmem50a (MGI:1919067)			
chr1	25360658	25430192	1p36.2-p34	1p36.11		111700	RHCE	Rhesus system C and E polypeptides	RHCE	6006	ENSG00000188672	?order: C-E-D	"[Blood group, Rhesus], 111690 (3); Rh-null disease, amorph type (3)"	Rhd (MGI:1202882)			
chr1	25430857	25500208	1p36.11	1p36.11		610301	"TMEM57, FLJ10747"	Transmembrane protein 57	MACO1	55219	ENSG00000204178			Tmem57 (MGI:1913396)			
chr1	25543584	25590399	1p36-p35	1p36.11		605747	"LDLRAP1, ARH, FHCB2, FHCB1"	Low density lipoprotein receptor adaptor protein 1	LDLRAP1	26119	ENSG00000157978		"Hypercholesterolemia, familial, autosomal recessive, 603813 (3), Autosomal recessive"	Ldlrap1 (MGI:2140175)			
chr1	25616819	25786206	1p36.13-p35.1	1p36.11		616772	MAN1C1	"Mannosidase, alpha, class 1C, member 1"	MAN1C1	57134	ENSG00000117643			Man1c1 (MGI:2446214)			
chr1	25800175	25818221	1p36-p35	1p36.11		606210	"SELENON, SEPN1, SELN, RSMD1, CFTD"	Selenoprotein N	SELENON	57190	ENSG00000162430		"Muscular dystrophy, rigid spine, 1, 602771 (3), Autosomal recessive; Myopathy, congenital, with fiber-type disproportion, 255310 (3), Autosomal recessive, Autosomal dominant"	Selenon (MGI:2151208)			
chr1	25861483	25876706	1p36.11	1p36.11		607779	"PAQR7, MPRA, PGLP"	"Progestin and ADIPOQ receptor family, member 7"	PAQR7	164091	ENSG00000182749			Paqr7 (MGI:1919154)			
chr1	25884185	25906876	1p36.1-p35	1p36.11		151442	"STMN1, LAP18, SMN"	Stathmin	STMN1	3925	ENSG00000117632			Stmn1 (MGI:96739)			
chr1	25959763	25998163	1p36.11	1p36.11		602344	PAFAH2	Platelet-activating factor acetylhydrolase 2	PAFAH2	5051	ENSG00000158006			Pafah2 (MGI:2140321)			
chr1	26021774	26036463	1p36.1	1p36.11		601738	EXTL1	Exostosin-like 1	EXTL1	2134	ENSG00000158008			Extl1 (MGI:1888742)			
chr1	26038021	26046137	1p36.11	1p36.11		609617	"SLC30A2, ZNT2, TNZD"	"Solute carrier family 30 (zinc transporter), member 2"	SLC30A2	7780	ENSG00000158014		"Zinc deficiency, transient neonatal, 608118 (3), Autosomal dominant"	Slc30a2 (MGI:106637)			
chr1	26051303	26067633	1p36.11	1p36.11		606131	"TRIM63, RNF28, SMRZ, MURF1"	Tripartite motif containing 63	TRIM63	84676	ENSG00000158022			Trim63 (MGI:2447992)			
chr1	26109130	26125547	1p35.3	1p36.11		610785	PDIK1L	PDLIM1-interacting kinase 1-like	PDIK1L	149420	ENSG00000175087			Pdik1l (MGI:2385213)			
chr1	26169896	26170872	1p36.11	1p36.11		616698	"ZNF593, ZT86"	Zinc finger protein 593	ZNF593	51042	ENSG00000142684			Zfp593 (MGI:1915290)			
chr1	26177489	26189883	1p36.11	1p36.11		603272	"CNKSR1, CNK1"	Connector enhancer of KSR 1	CNKSR1	10256	ENSG00000142675			Cnksr1 (MGI:2670958)			
chr1	26189961	26202541	1p35.3	1p36.11		609121	CATSPER4	"Cation channel, sperm-associated, 4"	CATSPER4	378807	ENSG00000188782			Catsper4 (MGI:3043288)			
chr1	26279721	26281521	1p36.11	1p36.11		615679	SH3BGRL3	SH3 domain-binding glutamic acid-rich protein-like protein 3	SH3BGRL3	83442	ENSG00000142669			Sh3bgrl3 (MGI:1920973)			
chr1	26282281	26318264	1p36.11	1p36.11		609151	"UBXN11, SOC"	UBX domain protein 11	UBXN11	91544	ENSG00000158062			Ubxn11 (MGI:1914836)			
chr1	26317919	26320522	1p36.11	1p36.11		114280	"CD52, CDW52"	CD52 molecule	CD52	1043	ENSG00000169442						
chr1	26361631	26374535	1p36.11	1p36.11		616775	"ZNF683, HOBIT"	Zinc finger protein 683	ZNF683	257101	ENSG00000176083						
chr1	26410767	26429727	1p36.11	1p36.11		611043	"LIN28, LIN28A"	"Lin28, C. elegans, homolog of"	LIN28A	79727	ENSG00000131914			Lin28a (MGI:1890546)			
chr1	26432281	26471305	1p36.11	1p36.11		608172	"DHDDS, HDS, RP59, DEDSM"	Dehydrodolichyl diphosphate synthase	DHDDS	79947	ENSG00000117682	mutation identified in 1 CDG1BB patient	"?Congenital disorder of glycosylation, type 1bb, 613861 (3), Autosomal recessive; Developmental delay and seizures with or without movement abnormalities, 617836 (3), Autosomal dominant; Retinitis pigmentosa 59, 613861 (3), Autosomal recessive"	Dhdds (MGI:1914672)			
chr1	26472410	26476641	1p36.1	1p36.11		163910	"HMGN2, HMG17"	High-mobility group nucleosomal binding protein 2	HMGN2	3151	ENSG00000198830						
chr1	26529757	26575028	1p36.1	1p36.11		601684	"RPS6KA1, RSK1"	"Ribosomal protein S6 kinase, 90kD, 1"	RPS6KA1	6195	ENSG00000117676			Rps6ka1 (MGI:104558)			
chr1	26696032	26782109	1p35.3	1p36.11		603024	"ARID1A, C1orf4, B120, SMARCF1, MRD14, CSS2"	"AT rich interactive domain 1A, SWI-like"	ARID1A	8289	ENSG00000117713		"Coffin-Siris syndrome 2, 614607 (3), Autosomal dominant"	Arid1a (MGI:1935147)			
chr1	26787962	26798402	1p36.11	1p36.11		610274	"PIGV, HPMRS1"	"Phosphatidylinositol glycan, class V"	PIGV	55650	ENSG00000060642		"Hyperphosphatasia with mental retardation syndrome 1, 239300 (3), Autosomal recessive"	Pigv (MGI:2442480)			
chr1	26863137	26864456	1p36.11	1p36.11		601290	SFN	Stratifin	SFN	2810	ENSG00000175793			Sfn (MGI:1891831)			
chr1	26890487	26900470	1p36.11	1p36.11		617486	GPATCH3	G-patch domain-containing protein 3	GPATCH3	63906	ENSG00000198746			Gpatch3 (MGI:2442492)			
chr1	26900568	26946870	1p36.11	1p36.11		610325	NUDC	"Nuclear distribution gene C, A. nigulans, homolog of"	NUDC	10726	ENSG00000090273			Nudc (MGI:106014)			
chr1	26911483	26914109	1p36.1	1p36.11		604630	"NR0B2, SHP"	"Nuclear receptor subfamily 0, group B, member 2"	NR0B2	8431	ENSG00000131910		"Obesity, mild, early-onset, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Nr0b2 (MGI:1346344)			
chr1	26949555	26960495	1p36	1p36.11		616758	"KDF1, C1orf172, ECTD12"	Keratinocyte differentiation factor 1	KDF1	126695	ENSG00000175707	mutation identified in 1 ECTD12 family	"?Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type, 617337 (3), Autosomal dominant"	Kdf1 (MGI:1916323)			
chr1	26993662	27000890	1p36.11	1p36.11		616824	TRNP1	TMF1-regulated nuclear protein 1	TRNP1	388610	ENSG00000253368			Trnp1 (MGI:1916789)			
chr1	27098808	27155129	1p36.1-p35	1p36.11		107310	"SLC9A1, NHE1, APNH, LIKNS"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 1 (antiporter, Na+/H+, amiloride sensitive)"	SLC9A1	6548	ENSG00000090020	mutation identified in 1 LIKNS family	"?Lichtenstein-Knorr syndrome, 616291 (3), Autosomal recessive"	Slc9a1 (MGI:102462)			
chr1	27341991	27353931	1p36.11	1p36.11		608042	"SYTL1, SLP1, JFC1"	Synaptotagmin-like protein 1	SYTL1	84958	ENSG00000142765			Sytl1 (MGI:1933365)			
chr1	27355178	27368036	1p36.11	1p36.11		604468	"MAP3K6, MAPKKK6, ASK2"	Mitogen-activated protein kinase kinase kinase 6	MAP3K6	9064	ENSG00000142733			Map3k6 (MGI:1855691)			
chr1	27369109	27374851	1p36.11	1p36.11		604973	"FCN3, HAKA1"	Ficolin 3	FCN3	8547	ENSG00000142748		"Immunodeficiency due to ficolin 3 deficiency, 613860 (3), Autosomal recessive"				
chr1	27392643	27395813	1p36.1-p34.3	1p36.11		600241	GPR3	G protein-coupled receptor-3	GPR3	2827	ENSG00000181773			Gpr3 (MGI:101908)			
chr1	27404225	27490186	1p36.11-p34.3	1p36.11		605875	"WASF2, WAVE2, SCAR2"	WAS protein family member 2	WASF2	10163	ENSG00000158195	?pseudogene on Xp11.21		Wasf2 (MGI:1098641)			
chr1	27534244	27604177	1p36.11	1p36.1-p35.3		615790	"AHDC1, MRD25"	AT-hook DNA-binding motif-containing protein 1	AHDC1	27245	ENSG00000126705		"Xia-Gibbs syndrome, 615829 (3), Autosomal dominant"	Ahdc1 (MGI:2444218)			
chr1	27600000	34300000	1p35			132850	EBVS1	Epstein-Barr virus integration site	EBVS1	1888							
chr1	27612288	27635560	1p36.2-p36.1	1p35.3		164940	"FGR, SRC2"	Oncogene FGR	FGR	2268	ENSG00000000938	same as SRC2		Fgr (MGI:95527)			
chr1	27666060	27672228	1p35	1p35.3		147572	"G1P3, IFI616"	"Interferon, alpha-inducible protein (clone IFI-6-16)"	IFI6	2537	ENSG00000126709						
chr1	27830740	27851671	1p35	1p35.3		602636	"PPP1R8, NIPP1, ARD1"	"Protein phosphatase-1, regulatory subunit-8"	PPP1R8	5511	ENSG00000117751			Ppp1r8 (MGI:2140494)			
chr1	27872530	27886684	1p35.3	1p35.3		617856	"THEMIS2, C1orf38, ICB1"	"Thymocyte selection-associated protein family, member 2"	THEMIS2	9473	ENSG00000130775			Themis2 (MGI:2446213)			
chr1	27891523	27914796	1p35	1p35.3		179836	RPA2	"Replication protein A2, 32kD"	RPA2	6118	ENSG00000117748			Rpa2 (MGI:1339939)			
chr1	27934954	27959156	1p35.3	1p35.3		617737	"SMPDL3B, ASML3B"	"Sphingolyelin phosphodiesterase, acid-like, 3B"	SMPDL3B	27293	ENSG00000130768			Smpdl3b (MGI:1916022)			
chr1	27970343	28088670	1p36	1p35.3		601655	EYA3	"Eyes absent, Drosophila, homolog of, 3"	EYA3	2140	ENSG00000158161			Eya3 (MGI:109339)			
chr1	28147165	28193935	1p35-p34.3	1p35.3		173393	PTAFR	Platelet-activating factor receptor	PTAFR	5724	ENSG00000169403			Ptafr (MGI:106066)			
chr1	28236090	28238104	1p35.3	1p35.3		614981	"ATP1F1, IF1"	ATPase inhibitory factor 1	ATP5IF1	93974	ENSG00000130770			Atpif1 (MGI:1196457)			
chr1	28259451	28282490	1p35.3	1p35.3		607767	"SEST2, HI95"	Sestrin 2	SESN2	83667	ENSG00000130766			Sesn2 (MGI:2651874)			
chr1	28329001	28335966	1p35.3	1p35.3		612384	MED18	Mediator complex subunit 18	MED18	54797	ENSG00000130772			Med18 (MGI:1914469)			
chr1	28369553	28500368	1p35.3	1p35.3		608726	PHACTR4	Phosphatase and actin regulator 4	PHACTR4	65979	ENSG00000204138			Phactr4 (MGI:2140327)			
chr1	28505942	28539195	1p36.1	1p35.3		179710	"CHC1, RCC1"	Regulator of chromosome condensation	RCC1	1104	ENSG00000180198			Rcc1 (MGI:1913989)			
chr1	28505942	28510891	1p36.1	1p35.3		603238	"RNU17D, U17HG"	"RNA, U17d small nucleolar"	SNHG3	8420							
chr1	28507364	28507570	1p36.1	1p35.3		180645	"RNU17A, RNE1"	"RNA, U17a small nucleolar"	SNORA73A	6080		in IVS1 of CHC1					
chr1	28508557	28508761	1p36.1	1p35.3		603239	RNU17B	"RNA, U17b small nucleolar"	SNORA73B	26768							
chr1	28603095	28648706	1p35.3	1p35.3		600773	TAF12	"TAF12 RNA polymerase II, TATA box-binding protein-associated factor, 20kD"	TAF12	6883	ENSG00000120656			Taf12 (MGI:1913714)			
chr1	28668727	28715602	1p35.3	1p35.3		604409	GMEB1	Glucocorticoid modulatory element-binding protein 1	GMEB1	10691	ENSG00000162419			Gmeb1 (MGI:2135604)			
chr1	28736620	28769774	1p35	1p35.3		610640	YTHDF2	YTH N6-methyladenosine RNA-binding protein 2	YTHDF2	51441	ENSG00000198492	fused with AML1 in t(1;21)		Ythdf2 (MGI:2444233)			
chr1	28812141	28863695	1p36.1-p34.3	1p35.3		165195	OPRD1	"Opioid receptor, delta-1"	OPRD1	4985	ENSG00000116329			Oprd1 (MGI:97438)			
chr1	28887090	29120045	1p36.2-p34	1p35.3		130500	"EPB41, EL1"	Erythrocyte surface protein band 4.1	EPB41	2035	ENSG00000159023		"Elliptocytosis-1, 611804 (3)"	Epb41 (MGI:95401)			
chr1	29147737	29182124	1p35.3	1p35.3		601940	"SRSF4, SFRS4, SRp75"	"Splicing factor, serine/arginine-rich, 4"	SRSF4	6429	ENSG00000116350			Srsf4 (MGI:1890577)			
chr1	29192656	29230957	1p35.3	1p35.3		608205	"MECR, NRBF1, DYTOABG"	Mitochondrial trans-2-enoyl-CoA reductase	MECR	51102	ENSG00000116353		"Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, 617282 (3), Autosomal recessive"	Mecr (MGI:1349441)			
chr1	29236515	29326812	1p35.3	1p35.3		602454	"PTPRU, GLEPP1, PTPU2"	"Protein tyrosine phosphatase, receptor type, U"	PTPRU	10076	ENSG00000060656			Ptpru (MGI:1321151)			
chr1	30711276	30723584	1p35	1p35.2		115437	"MATN1, CRTM, CMP"	"Matrilin 1, cartilage matrix protein"	MATN1	4146	ENSG00000162510			Matn1 (MGI:106591)			
chr1	30732467	30757839	1p34	1p35.2		601476	LAPTM5	Lysosomal-associated multispanning membrane protein-5	LAPTM5	7805	ENSG00000162511			Laptm5 (MGI:108046)			
chr1	30869465	30909734	1pter-p22.3	1p35.2		186357	"SDC3, SYND3, SDCN"	Syndecan 3	SDC3	9672	ENSG00000162512		"{Obesity, association with}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Sdc3 (MGI:1349163)			
chr1	30931505	31065716	1p35.2	1p35.2		607204	"PUM1, KIAA0099"	"Pumilio, Drosophila, homolog of, 1"	PUM1	9698	ENSG00000134644			Pum1 (MGI:1931749)			
chr1	31179269	31239886	1p35.2	1p35.2		612871	NKAIN1	Na+/K+ transporting ATPase-interacting 1	NKAIN1	79570	ENSG00000084628			Nkain1 (MGI:1914399)			
chr1	31259567	31296796	1p35.2	1p35.2		607797	"SNRNP40, SPF38, PRPF8BP"	Small nuclear ribonucleoprotein 40kDa (U5)	SNRNP40	9410	ENSG00000060688			Snrnp40 (MGI:1913835)			
chr1	31359594	31373617	1p33-p31	1p35.2		134651	FABP3	"Fatty acid-binding protein 3, muscle"	FABP3	2170	ENSG00000121769			Fabp3 (MGI:95476)			
chr1	31409564	31434679	1p35.2	1p35.2		614549	SERINC2	Serine incorporator 2	SERINC2	347735	ENSG00000168528			Serinc2 (MGI:1919132)			
chr1	31576383	31587685	1p35.2	1p35.2		616064	"TINAGL1, TINAGRP"	Tubulointerstitial nephritis antigen-like protein 1	TINAGL1	64129	ENSG00000142910			Tinagl1 (MGI:2137617)			
chr1	31617699	31632517	1p35.2	1p35.2		602392	"HCRTR1, OX1R"	Hypocretin receptor 1	HCRTR1	3061	ENSG00000121764			Hcrtr1 (MGI:2385650)			
chr1	31629861	31645236	1p34	1p35.2		610033	PEF1	Peflin	PEF1	553115	ENSG00000162517			Pef1 (MGI:1915148)			
chr1	31652246	31704166	1p34	1p35.2		120326	COL16A1	"Collagen XVI, alpha-1 polypeptide"	COL16A1	1307	ENSG00000084636			Col16a1 (MGI:1095396)			
chr1	31727104	31764062	1p35	1p35.2		602683	"ADGRB2, BAI2"	Adhesion G protein-coupled receptor B2	ADGRB2	576	ENSG00000121753			Adgrb2 (MGI:2451244)			
chr1	31906420	31938386	1p35	1p35.2		601584	"PTP4A2, PTP4A, PRL2, HH13"	"Protein tyrosine phosphatase, type 4A, 2"	PTP4A2	8073	ENSG00000184007			Ptp4a2 (MGI:1277117)			
chr1	32013693	32060858	1p32	1p35.2		602489	"KHDRBS1, SAM68"	"KH domain-containing, RNA-binding, signal transduction-associated protein 1"	KHDRBS1	10657	ENSG00000121774			Khdrbs1 (MGI:893579)			
chr1	32108042	32176567	1p35.1	1p35.2		610563	KPNA6	Karyopherin alpha-6	KPNA6	23633	ENSG00000025800			Kpna6 (MGI:1100836)			
chr1	32200385	32205389	1p35.1	1p35.2		610162	"CCDC28B, MGC1203"	Coiled-coil domain-containing protein 28B	CCDC28B	79140	ENSG00000160050		"{Bardet-Biedl syndrome 1, modifier of}, 209900 (3), Autosomal recessive, Digenic recessive"	Ccdc28b (MGI:1913514)			
chr1	32221583	32231603	1p34.1	1p35.2		603911	"EIF3I, EIF3S2, TRIP1"	"Eukaryotic translation initiation factor 3, subunit I"	EIF3I	8668	ENSG00000084623	pseudogene on 7q32		Eif3i (MGI:1860763)			
chr1	32251238	32286166	1p35-p34.3	1p35.2		153390	"LCK, IMD22"	Lymphocyte-specific protein tyrosine kinase	LCK	3932	ENSG00000182866	LCK/TCRB fusion in leukemia; mutation identified in 1 IMD22 patient	"?Immunodeficiency 22, 615758 (3), Autosomal recessive"	Lck (MGI:96756)			
chr1	32292102	32333627	1p34.1	1p35.2-p35.1		601241	"HDAC1, RPD3L1"	Histone deacetylase-1	HDAC1	3065	ENSG00000116478			Hdac1 (MGI:108086)			
chr1	32333828	32336238	1p34	1p35.1		602940	"MARCKSL1, MLP, MRP"	MARCKS-like protein 1	MARCKSL1	65108	ENSG00000175130			Marcksl1 (MGI:97143)			
chr1	32352719	32365264	1p35-p34	1p35.1		607660	"TSSK3, STK22C, STK22D"	Testis-specific serine/threonine kinase 3	TSSK3	81629	ENSG00000162526			Tssk3 (MGI:1929914)			
chr1	32364632	32394460	1p35.1	1p35.1		617518	BSDC1	BSD domain-containing protein 1	BSDC1	55108	ENSG00000160058			Bsdc1 (MGI:1913466)			
chr1	32620817	32651007	1p35.1	1p35.1		615891	"ZBTB8OS, ARCH"	"Zinc finger- and BTB domain-containing protein 8, opposite strand"	ZBTB8OS	339487	ENSG00000176261			Zbtb8os (MGI:1914356)			
chr1	32679905	32703595	1p34.3-p34.1	1p35.1		611750	SYNC1	Syncoilin 1	SYNC	81493				Sync (MGI:1916078)			
chr1	32775237	32818031	1p35	1p35.1		603623	"YARS, CMTDIC, TYRRS, YTS, YRS"	Tyrosyl-tRNA synthetase	YARS	8565	ENSG00000134684		"Charcot-Marie-Tooth disease, dominant intermediate C, 608323 (3), Autosomal dominant"	Yars (MGI:2147627)			
chr1	32816766	32858878	1p34.3	1p35.1		611889	"S100PBP, S100PBPR"	S100P-binding protein	S100PBP	64766	ENSG00000116497			S100pbp (MGI:1921898)			
chr1	32862267	32872491	1p35.1	1p35.1		611906	"FNDC5, FRCP2"	Fibronectin type III domain-containing protein 5	FNDC5	252995	ENSG00000160097			Fndc5 (MGI:1917614)			
chr1	32885964	32894645	1p35-p34.2	1p35.1		142622	"HPCA, DYT2"	"Hippocalcin, 23kD, Ca2+-binding protein"	HPCA	3208	ENSG00000121905		"Dystonia 2, torsion, autosomal recessive, 224500 (3), Autosomal recessive"	Hpca (MGI:1336200)			
chr1	32932497	32965265	1p35.1	1p35.1		610872	"IBRDC3, NKLAM"	IBR domain-containing protein 3	RNF19B	127544	ENSG00000116514			Rnf19b (MGI:1922484)			
chr1	33007939	33036910	1p34	1p35.1		103020	AK2	"Adenylate kinase-2, mitochondrial"	AK2	204	ENSG00000004455		"Reticular dysgenesis, 267500 (3), Autosomal recessive"	Ak2 (MGI:87978)			
chr1	33081109	33162287	1p34.3-p33	1p35.1		608353	"AZIN2, ODC1L, KIAA1945"	Antizyme inhibitor 2	AZIN2	113451	ENSG00000142920			Azin2 (MGI:2442093)			
chr1	33145398	33184773	1p35.1	1p35.1		616755	"TRIM62, DEAR1"	Tripartite motif-containing protein 62	TRIM62	55223	ENSG00000116525			Trim62 (MGI:1914775)			
chr1	33472590	33504252	1p35.1	1p35.1		611315	"ZSCAN20, ZNF31, KOX29"	Zinc finger- and SCAN domain-containing protein 20	ZSCAN20	7579	ENSG00000121903			Zscan20 (MGI:2679268)			
chr1	33513998	34165841	1p35.3	1p35.1		608398	"CSMD2, KIAA1884"	Cub and Sushi multiple domains 2	CSMD2	114784	ENSG00000121904			Csmd2 (MGI:2386401)			
chr1	33860474	33864790	1p35.1	1p35.1		617285	HMGB4	High mobility group box 4	HMGB4	127540	ENSG00000176256			Hmgb4 (MGI:1916567)			
chr1	34300000	39600000	1p34.3			609919	GBD3	Gallbladder disease 3	GBD3	100048906		new D2S255	"Gallbladder disease 3, 609919 (2)"				
chr1	34300000	60800000	1p34-p32			613545	MACST	Macrostomia		100529231		max lod at D1S2797	"Macrostomia, 613545 (2)"				
chr1	34754776	34758512	1p35.1	1p34.3		604493	"GJB5, CX31.1"	"Gap junction protein, beta-5"	GJB5	2709	ENSG00000189280			Gjb5 (MGI:95723)			
chr1	34759740	34763723	1p35.1	1p34.3		605425	"GJB4, CX30.3, EKVP2"	"Gap junction protein, beta-4"	GJB4	127534	ENSG00000189433		"Erythrokeratodermia variabilis et progressiva 2, 617524 (3), Autosomal dominant"	Gjb4 (MGI:95722)			
chr1	34781188	34786365	1p35.1	1p34.3		603324	"GJB3, CX31, DFNA2B, EKVP1"	"Gap junction protein, beta-3"	GJB3	2707	ENSG00000188910	same YAC as GJA4	"Deafness, autosomal dominant 2B, 612644 (3), Autosomal dominant; Deafness, autosomal dominant, with peripheral neuropathy (3); Deafness, autosomal recessive (3); Deafness, digenic, GJB2/GJB3, 220290 (3), Autosomal recessive; Erythrokeratodermia variabilis et progressiva 1, 133200 (3), Autosomal recessive, Autosomal dominant"	Gjb3 (MGI:95721)			
chr1	34792957	34795746	1p35.1	1p34.3		121012	"GJA4, CX37"	"Gap junction protein, alpha-4, 37kD (connexin 37)"	GJA4	2701	ENSG00000187513			Gja4 (MGI:95715)			
chr1	34986164	35031967	14q12	1p34.3		613567	"ZMYM6, ZNF258"	"Zinc finger, MYM-type 6"	ZMYM6	9204	ENSG00000163867			Zmym6 (MGI:106505)			
chr1	35176377	35193173	1p34	1p34.3		605199	"SFPQ, PSF"	"Splicing factor, proline- and glutamine-rich"	SFPQ	6421	ENSG00000116560	fusion gene with TFE3 in RCC		Sfpq (MGI:1918764)			
chr1	35268693	35421943	1p34.3	1p34.3		613568	"ZMYM4, ZNF262, KIAA0425"	"Zinc finger, MYM-type 4"	ZMYM4	9202	ENSG00000146463			Zmym4 (MGI:1915035)			
chr1	35433489	35557602	1p34.3	1p34.3		613535	"KIAA0319L, KIAA1837"	KIAA0319-like	KIAA0319L	79932	ENSG00000142687			AU040320 (MGI:2140475)			
chr1	35557791	35566778	1p34.3	1p34.3		608458	"NCDN, KIAA0607"	Neurochondrin	NCDN	23154	ENSG00000020129			Ncdn (MGI:1347351)			
chr1	35568738	35595590	1p34.3	1p34.3		614428	TFAP2E	Transcription factor AP2-epsilon	TFAP2E	339488	ENSG00000116819			Tfap2e (MGI:2679630)			
chr1	35599540	35641843	1p34.2	1p34.3		602175	PSMB2	"Proteasome subunit, beta type, 2"	PSMB2	5690	ENSG00000126067			Psmb2 (MGI:1347045)			
chr1	35720217	35769984	1p34.3-p34.1	1p34.3		605434	CLASPIN	"Claspin, Xenopus, homolog of"	CLSPN	63967	ENSG00000092853			Clspn (MGI:2445153)			
chr1	35807623	35857889	1p35-p34	1p34.3		607356	"EIF2C4, AGO4, KIAA1567"	"Eukaryotic translation initiation factor 2C, 4 (argonaute 4)"	AGO4	192670	ENSG00000134698			Ago4 (MGI:1924100)			
chr1	35869807	35929609	1p35-p34	1p34.3		606228	"AGO1, EIF2C1, GERP95, EIF2C"	"Argonaute 1, RISC catalytic component"	AGO1	26523	ENSG00000092847			Ago1 (MGI:2446630)			
chr1	35925682	36056469	1p35-p34	1p34.3		607355	"EIF2C3, AGO3"	"Eukaryotic translation initiation factor 2C, subunit 3 (argonaute 3)"	AGO3	192669	ENSG00000126070			Ago3 (MGI:2446634)			
chr1	36088851	36093931	1p35.3-p34.1	1p34.3		610624	"ADPRHL2, ARH3"	ADP-ribosylhydrolase-like 2	ADPRHL2	54936	ENSG00000116863			Adprhl2 (MGI:2140364)			
chr1	36095235	36126206	1p34.3-p32.3	1p34.3		120252	"COL8A2, FECD1, PPCD2"	"Collagen VIII, alpha-2 polypeptide"	COL8A2	1296	ENSG00000171812		"Corneal dystrophy, Fuchs endothelial, 1, 136800 (3), Autosomal dominant; Corneal dystrophy, posterior polymorphous 2, 609140 (3), Autosomal dominant"	Col8a2 (MGI:88464)			
chr1	36136568	36156052	1p34.3	1p34.3		610955	"TRAPPC3, BET3"	"Trafficking protein particle complex, subunit 3"	TRAPPC3	27095	ENSG00000054116			Trappc3 (MGI:1351486)			
chr1	36224411	36305356	1p34.3	1p34.3		603809	"THRAP3, TRAP150"	Thyroid hormone receptor-associated protein 3	THRAP3	9967	ENSG00000054118			Thrap3 (MGI:2442637)			
chr1	36339618	36385926	1p34.3	1p34.3		609437	"STK40, SHIK"	Serine/threonine protein kinase 40	STK40	83931	ENSG00000196182			Stk40 (MGI:1921428)			
chr1	36393419	36397958	1p34.3	1p34.3		617909	LSM10	"Lsm10, U7 small nuclear RNA-associated protein"	LSM10	84967	ENSG00000181817			Lsm10 (MGI:2151045)			
chr1	36417905	36450484	1p34.2	1p34.3		608854	NOR1	Oxidored-nitro domain-containing protein 1	OSCP1	127700	ENSG00000116885			Oscp1 (MGI:1916308)			
chr1	36455760	36464438	1p35-p34.1	1p34.3		611979	MRPS15	Mitochondrial ribosomal protein S15	MRPS15	64960	ENSG00000116898			Mrps15 (MGI:1913657)			
chr1	36466042	36483313	1p35-p34.3	1p34.3		138971	"CSF3R, GCSFR, SCN7"	Colony-stimulating factor-3 receptor (granulocyte)	CSF3R	1441	ENSG00000119535		"Neutropenia, severe congenital, 7, autosomal recessive, 617014 (3), Autosomal recessive"	Csf3r (MGI:1339755)			
chr1	36795526	37034242	1p34-p33	1p34.3		138243	"GRIK3, GLUR7"	"Glutamate receptor, ionotropic, kainate 3"	GRIK3	2899	ENSG00000163873			Grik3 (MGI:95816)			
chr1	37474517	37484376	1p35.3-p33	1p34.3		610562	"ZC3H12A, MCPIP, MCPIP1"	Zinc finger CCCH domain-containing protein 12A	ZC3H12A	80149	ENSG00000163874			Zc3h12a (MGI:2385891)			
chr1	37489959	37514818	1p35.3-p33	1p34.3		611001	"MEAF6, C1orf149, EAF6"	MYST/ESA1-associated factor 6	MEAF6	64769	ENSG00000163875			Meaf6 (MGI:1917338)			
chr1	37534448	37554343	1p34.3	1p34.3		608241	"SNIP1, PMRED"	SMAD nuclear interacting protein 1	SNIP1	79753	ENSG00000163877		"Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501 (3), Autosomal recessive"	Snip1 (MGI:2156003)			
chr1	37556918	37566856	1p35.1	1p34.3		602135	"DNALI1, P28"	"Dynein, axonemal, light intermediate polypeptide 1"	DNALI1	7802	ENSG00000163879			Dnali1 (MGI:1922813)			
chr1	37566811	37595984	1p34.3	1p34.3		609365	"GNL2, NGP1"	Guanine nucleotide-binding protein-like 2	GNL2	29889	ENSG00000134697			Gnl2 (MGI:2385207)			
chr1	37611349	37634922	1p34.3	1p34.3		609595	"RSPO1, FLJ40906"	"Roof plate-specific spondin, mouse, homolog of, 1"	RSPO1	284654	ENSG00000169218		"Palmoplantar hyperkeratosis and true hermaphroditism, 610644 (3), Autosomal recessive; Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal, 610644 (3), Autosomal recessive"	Rspo1 (MGI:2183426)			
chr1	37681569	37692335	1p34.3	1p34.3		614799	C1orf109	Chromosome 1 open reading frame 109	C1orf109	54955	ENSG00000116922			9930104L06Rik (MGI:3041172)			
chr1	37692400	37709718	1p34.3	1p34.3		609977	CDCA8	Cell division cycle-associated protein 8	CDCA8	55143	ENSG00000134690	possible pseudogene on chr.7		Cdca8 (MGI:1196274)			
chr1	37713887	37765151	1p34.3	1p34.3		611123	EPHA10	Ephrin receptor EphA10	EPHA10	284656	ENSG00000183317			Epha10 (MGI:3586824)			
chr1	37802941	37808192	1p34.2	1p34.3		612276	"YRDC, IRIP"	YRDC domain-containing protein	YRDC	79693	ENSG00000196449			Yrdc (MGI:2387201)			
chr1	37809566	37859619	1p33	1p34.3		600172	MTF1	Metal-regulatory transcription factor 1	MTF1	4520	ENSG00000188786			Mtf1 (MGI:101786)			
chr1	37860696	37947094	1p34	1p34.3		147264	INPP5B	"Inositol polyphosphate-5-phosphatase, 75kD"	INPP5B	3633	ENSG00000204084			Inpp5b (MGI:103257)			
chr1	37956974	37990109	1p34.3	1p34.3		605596	"SF3A3, SF3A60, SAP61, PRP9"	"Splicing factor 3A, subunit 3"	SF3A3	10946	ENSG00000183431			Sf3a3 (MGI:1922312)			
chr1	37996764	38005690	1p34	1p34.3		602790	"FHL3, SLIM2"	Four-and-a-half LIM domains-3	FHL3	2275	ENSG00000183386			Fhl3 (MGI:1341092)			
chr1	38012711	38024824	1p34.3	1p34.3		609440	"UTP11L, CGI94"	UTP11-like protein	UTP11	51118	ENSG00000183520			Utp11 (MGI:1914455)			
chr1	38043850	38046777	1p34.1	1p34.3		602479	POU3F1	"POU domain, class 3, transcription factor-1"	POU3F1	5453	ENSG00000185668						
chr1	38838196	38859822	1p34	1p34.3		608267	"RRAGC, RAGC"	RAS-related GTP-binding protein C	RRAGC	64121	ENSG00000116954			Rragc (MGI:1858751)			
chr1	38862489	38873377	1p33-p32.2	1p34.3		606535	MYCBP	MYC-binding protein	MYCBP	26292	ENSG00000214114			Mycbp (MGI:1891750)			
chr1	38874066	38881625	1p34.3	1p34.3		611923	"GJA9, CX59"	"Gap junction protein, alpha-9"	GJA9	81025	ENSG00000131233						
chr1	38991243	39006064	1p34.3	1p34.3		615164	AKIRIN1	Akirin 1	AKIRIN1	79647	ENSG00000174574			Akirin1 (MGI:1915300)			
chr1	39026294	39034635	1p34.2-p33	1p34.3		603847	NDUFS5	"NADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kD"	NDUFS5	4725	ENSG00000168653						
chr1	39084166	39487137	1p32-p31	1p34.3		608271	"MACF1, ACF7, KIAA1251"	Microtubule-actin cross-linking factor 1	MACF1	23499	ENSG00000127603						
chr1	39560812	39576848	1p36-p32	1p34.3		603407	"PABPC4, PABP4, IPABP, APP1"	"Polyadenylate-binding protein, cytoplasmic, 4"	PABPC4	8761	ENSG00000090621			Pabpc4 (MGI:2385206)			
chr1	39623430	39639675	1p34.3	1p34.2		609034	HEYL	Hariy/enhancer of split-related with YRPW motif-like protein	HEYL	26508				Heyl (MGI:1860511)			
chr1	39659120	39672037	1p34.3-p33	1p34.2		610525	"NT5C1A, CN1A, CNI, CN1"	"5'-nucleotidase, cytosolic, IA"	NT5C1A	84618	ENSG00000116981			Nt5c1a (MGI:2155700)			
chr1	39738844	39765697	1p34.2	1p34.2		602435	"PPIE, CYP33"	Peptidyl-prolyl isomerase E	PPIE	10450	ENSG00000084072			Ppie (MGI:1917118)			
chr1	39757181	39788860	1p34.2	1p34.2		602284	"BMP8B, OP2"	Bone morphogenetic protein-8b (osteogenic protein 2)	BMP8B	656	ENSG00000116985						
chr1	39769524	39771347	1p34.2	1p34.2		610289	"OXCT2, FLJ0030"	3-oxoacid CoA transferase 2	OXCT2	64064	ENSG00000198754						
chr1	39841030	39883510	1p34.2	1p34.2		617840	"TRIT1, IPT, COXPD35"	tRNA isopentenyltransferase 1	TRIT1	54802	ENSG00000043514		"Combined oxidative phosphorylation deficiency 35, 617873 (3), Autosomal recessive"	Trit1 (MGI:1914216)			
chr1	39895423	39902014	1p34.3	1p34.2		164850	"MYCL, LMYC"	"Oncogene MYC, lung carcinoma-derived"	MYCL	4610	ENSG00000116990			Mycl (MGI:96799)			
chr1	39955111	39969967	1p34.2	1p34.2		614397	"MFSD2A, MCPH15"	Major facilitator superfamily domain-containing protein 2A	MFSD2A	84879	ENSG00000168389		"Microcephaly 15, primary, autosomal recessive, 616486 (3), Autosomal recessive"	Mfsd2a (MGI:1923824)			
chr1	40040064	40072648	1p34.2	1p34.2		617801	CAP1	Cyclase-associated actin cytoskeleton regulatory protein 1	CAP1	10487	ENSG00000131236			Cap1 (MGI:88262)			
chr1	40072705	40097469	1p32	1p34.2		600722	"PPT1, CLN1"	Palmitoyl-protein thioesterase 1	PPT1	5538	ENSG00000131238		"Ceroid lipofuscinosis, neuronal, 1, 256730 (3), Autosomal recessive"	Ppt1 (MGI:1298204)			
chr1	40161368	40240920	1p32	1p34.2		180610	RLF	Rearranged L-myc fusion sequence	RLF	6018	ENSG00000117000	<800kb from MYCL1		Rlf (MGI:1924705)			
chr1	40258049	40294183	1p34	1p34.2		606480	"ZMPSTE24, FACE1, STE24, MADB"	Zinc metalloproteinase STE24	ZMPSTE24	10269	ENSG00000084073		"Mandibuloacral dysplasia with type B lipodystrophy, 608612 (3), Autosomal recessive; Restrictive dermopathy, lethal, 275210 (3), Autosomal recessive"	Zmpste24 (MGI:1890508)			
chr1	40300486	40317652	1p34.2	1p34.2		120260	"COL9A2, EDM2, STL5"	"Collagen IX, alpha-2 polypeptide"	COL9A2	1298	ENSG00000049089	mutation identified in1 STL5 family	"Epiphyseal dysplasia, multiple, 2, 600204 (3), Autosomal dominant; ?Stickler syndrome, type V, 614284 (3), Autosomal recessive"	Col9a2 (MGI:88466)			
chr1	40373671	40423325	1p34.2	1p34.2		616916	"SMAP2, SMAP1L"	Small ADP-ribosylation factor GTPase-activating protein 2	SMAP2	64744	ENSG00000084070			Smap2 (MGI:1917030)			
chr1	40620679	40692103	1p34.1	1p34.2		611600	"RIMS3, NIM3, KIAA0137"	Protein regulating synaptic membrane exocytosis 3	RIMS3	9783	ENSG00000117016			Rims3 (MGI:2443331)			
chr1	40691569	40771602	1p32	1p34.2		605344	"NFYC, CBFC"	"Nuclear transcription factor Y, gamma"	NFYC	4802	ENSG00000066136			Nfyc (MGI:107901)			
chr1	40757283	40757371	1p34.2	1p34.2		615151	MIR30C1	Micro RNA 30C-1	MIR30C1	407031							
chr1	40784011	40840456	1p34	1p34.2		603537	"KCNQ4, DFNA2A"	"Potassium voltage-gated channel, KQT-like subfamily, member 4"	KCNQ4	9132	ENSG00000117013		"Deafness, autosomal dominant 2A, 600101 (3), Autosomal dominant"	Kcnq4 (MGI:1926803)			
chr1	40861055	40862345	1p35-p34	1p34.2		606815	CITED4	"CBP/P300-interacting transactivator, with glu/asp-rich carboxy terminal domain, 4"	CITED4	163732	ENSG00000179862			Cited4 (MGI:1861694)			
chr1	40979298	41012564	1p34.1	1p34.2		123860	"CTPS1, CTPS, IMD24"	Cytidine 5'-triphosphate synthetase 1	CTPS1	1503	ENSG00000171793		"Immunodeficiency 24, 615897 (3), Autosomal recessive"	Ctps (MGI:1858304)			
chr1	41027198	41242153	1p34	1p34.2		616396	SCMH1	"Sex comb on midleg, Drosophila, homolog of, 1"	SCMH1	22955	ENSG00000010803			Scmh1 (MGI:1352762)			
chr1	41361930	41383590	1p34.1	1p34.2		611457	FOXO6	Forkhead box O6	FOXO6	100132074	ENSG00000204060			Foxo6 (MGI:2676586)			
chr1	41478774	41484698	1p34	1p34.2		131241	EDN2	Endothelin-2	EDN2	1907	ENSG00000127129	vasoactive intestinal contractor (VIC) = mouse and rat equivalent		Edn2 (MGI:95284)			
chr1	41506364	42035924	1p34	1p34.2		606649	"HIVEP3, KRC"	Human immunodeficiency virus type 1 enhancer-binding protein 3	HIVEP3	59269	ENSG00000127124			Hivep3 (MGI:106589)			
chr1	42153420	42155823	1p34-p33	1p34.2		601271	"GUCA2B, UGN"	Guanylate cyclase activator 2B (uroguanylin)	GUCA2B	2981	ENSG00000044012			Guca2b (MGI:1270851)			
chr1	42162690	42164723	1p35-p34	1p34.2		139392	"GUCA2A, GUCA2"	"Guanylate cyclase activator 2A (guanylin 2, intestinal, heat-stable)"	GUCA2A	2980	ENSG00000197273			Guca2a (MGI:102738)			
chr1	42176538	42336804	1p34.2	1p34.2		616035	"FOXJ3, KIAA1041"	Forkhead box J3	FOXJ3	22887	ENSG00000198815			Foxj3 (MGI:2443432)			
chr1	42456340	42473380	1p13.1-p12	1p34.2		609853	PPCS	Phosphopantothenoylcysteine synthetase	PPCS	79717	ENSG00000127125			Ppcs (MGI:1915237)			
chr1	42657769	42681653	1p34.1	1p34.2		606095	PPIH	Peptidyl-prolyl isomerase H	PPIH	10465	ENSG00000171960			Ppih (MGI:106499)			
chr1	42682234	42703802	1p34	1p34.2		154030	"YBX1, NSEP1, YB1, DBPB"	"Y box binding protein 1 (major histocompatibility complex, class II, Y box-binding protein I)"	YBX1	4904	ENSG00000065978			Ybx1 (MGI:99146)			
chr1	42733092	42740253	1p34.2	1p34.2		610036	"CLDN19, HOMG5"	Claudin 19	CLDN19	149461	ENSG00000164007		"Hypomagnesemia 5, renal, with ocular involvement, 248190 (3), Autosomal recessive"	Cldn19 (MGI:3033992)			
chr1	42746334	42767083	1p34	1p34.2		610339	"P3H1, LEPRE1, GROS1, OI8"	Prolyl 3-hydroxylase 1	P3H1	64175	ENSG00000117385		"Osteogenesis imperfecta, type VIII, 610915 (3), Autosomal recessive"	P3h1 (MGI:1888921)			
chr1	42807051	42817387	1p34.2	1p34.2		617853	"SVBP, CCDC23"	Small vasohibin-binding protein	SVBP	374969	ENSG00000177868			Svbp (MGI:1916466)			
chr1	42817104	42844988	1p34	1p34.2		609017	"ERMAP, SC, RD"	Erythroblast membrane-associated protein	ERMAP	114625	ENSG00000164010		"[Blood group, Radin], 111620 (3); [Blood group, Scianna system], 111750 (3)"	Ermap (MGI:1349816)			
chr1	42925374	42959175	1p34.2	1p34.2		138140	"SLC2A1, GLUT1, HTLVR, DYT18, PED, GLUT1DS, EIG12, DYT9, SDCHCN"	"Solute carrier family 2 (facilitated glucose transporter), member 1"	SLC2A1	6513	ENSG00000117394	probably in 1p33	"Dystonia 9, 601042 (3), Autosomal dominant; {Epilepsy, idiopathic generalized, susceptibility to, 12}, 614847 (3), Autosomal dominant; GLUT1 deficiency syndrome 1, infantile onset, severe, 606777 (3), Autosomal recessive, Autosomal dominant; GLUT1 deficiency syndrome 2, childhood onset, 612126 (3), Autosomal dominant; Stomatin-deficient cryohydrocytosis with neurologic defects, 608885 (3), Autosomal dominant"	Slc2a1 (MGI:95755)			
chr1	43164173	43172569	1p35-p33	1p34.2		614443	"EBNA1BP2, EBP2"	EBNA1-binding protein 2	EBNA1BP2	10969	ENSG00000117395			Ebna1bp2 (MGI:1916322)			
chr1	43172329	43254357	1p34.2	1p34.2		614259	WDR65	WD repeat-containing protein 65	CFAP57	149465	ENSG00000243710			Cfap57 (MGI:2686209)			
chr1	43300894	43323109	1p34-p33	1p34.2		600222	"TIE, JTK14, TIE1"	Tyrosine kinase with immunoglobulin and epidermal growth factor homology domains	TIE1	7075	ENSG00000066056			Tie1 (MGI:99906)			
chr1	43336874	43354463	1p34	1p34.2		159530	"MPL, TPOR, MPLV, THCYT2"	"Myeloproliferative leukemia virus, homolog of"	MPL	4352	ENSG00000117400		"Myelofibrosis with myeloid metaplasia, somatic, 254450 (3); Thrombocythemia 2, 601977 (3), Autosomal dominant, Somatic mutation; Thrombocytopenia, congenital amegakaryocytic, 604498 (3), Autosomal recessive"	Mpl (MGI:97076)			
chr1	43358954	43363202	1p34.2-p33	1p34.2		603618	CDC20	"Cell division cycle 20, S. cerevisiae, homolog of"	CDC20	991	ENSG00000117399	pseudogene on 9q13-q21		Cdc20 (MGI:1859866)			
chr1	43363396	43368073	1p34.2	1p34.2		611813	"ELOVL1, SSC1"	Elongation of very long chain fatty acids-like 1	ELOVL1	64834	ENSG00000066322			Elovl1 (MGI:1858959)			
chr1	43383907	43389811	1p34.2	1p34.2		607956	MED8	Mediator complex subunit 8	MED8	112950	ENSG00000159479			Med8 (MGI:1915269)			
chr1	43389883	43454246	1p34.2	1p34.2		615463	"SZT2, KIAA0467, EIEE18"	"Seizure threshold 2, mouse, homolog of"	SZT2	23334	ENSG00000198198		"Epileptic encephalopathy, early infantile, 18, 615476 (3), Autosomal recessive"	Szt2 (MGI:3033336)			
chr1	43522237	43623671	1p32	1p34.2		179590	"PTPRF, LAR, BNAH2"	"Protein tyrosine phosphatase, receptor type, f polypeptide"	PTPRF	5792	ENSG00000142949	mutation identified in 1 BNAH2 family	"?Breasts and/or nipples, aplasia or hypoplasia of, 2, 616001 (3), Autosomal recessive"	Ptprf (MGI:102695)			
chr1	43650125	43705517	1p34.1	1p34.2-p34.1		609764	"KDM4A, JMJD2A, JHDM3A, KIAA0677"	Lysine-specific demethylase 4A	KDM4A	9682	ENSG00000066135			Kdm4a (MGI:2446210)			
chr1	43700000	60800000	1p34.1-p32			178300	PTOS1	"Ptosis, congenital 1, autosomal dominant"	PTOS1	5765			"Ptosis, hereditary congenital, 1, 178300 (2), Autosomal dominant"				
chr1	43707464	43931164	1p34.1	1p34.1		606494	"ST3GAL3, SIAT6, ST3GALII, MRT12, EIEE15"	"ST3 beta-galactoside alpha-2,3-sialyltransferase 3"	ST3GAL3	6487	ENSG00000126091	mutation identified in 1 EIEE15 family	"?Epileptic encephalopathy, early infantile, 15, 615006 (3), Autosomal recessive; Mental retardation, autosomal recessive 12, 611090 (3), Autosomal recessive"	St3gal3 (MGI:1316659)			
chr1	43946805	43968021	1p34.1	1p34.1		610411	"IPO13, IMP13, KIAA0724, RANBP13"	Importin 13	IPO13	9670	ENSG00000117408			Ipo13 (MGI:2385205)			
chr1	43969980	43973370	1p34	1p34.1		603456	"DPH2, DPH2L2"	"DPH2, S. cerevisiae, homolog of"	DPH2	1802	ENSG00000132768			Dph2 (MGI:1914978)			
chr1	43974647	43978299	1p32.3	1p34.1		603717	"ATP6V0B, ATP6F"	"ATPase, H+ transporting, lysosomal 21kD, V0 subunit c''"	ATP6V0B	533	ENSG00000117410			Atp6v0b (MGI:1890510)			
chr1	43979201	43991170	1p33-p32	1p34.1		604013	B4GALT2	"Beta-1,4-galactosyltransferase 2"	B4GALT2	8704	ENSG00000117411			B4galt2 (MGI:1858493)			
chr1	43996482	44031491	1p33	1p34.1		601019	"SLC6A9, GLYT1, GCENSG"	"Solute carrier family 6 (neurotransmitter transporter, glycine), member 9"	SLC6A9	6536	ENSG00000196517		"Glycine encephalopathy with normal serum glycine, 617301 (3), Autosomal recessive"	Slc6a9 (MGI:95760)			
chr1	44043926	44135139	1p34.1	1p34.1		609602	ZNF393	Zinc finger protein-393	KLF17	128209	ENSG00000171872			Klf17 (MGI:2181068)			
chr1	44213443	44220678	1p34.1	1p34.1		605077	"DNMAP1, DMAP1"	DNMT1-associated protein 1	DMAP1	55929	ENSG00000178028			Dmap1 (MGI:1913483)			
chr1	44221069	44355297	1p32	1p34.1		609917	"PRNPIP, PINT1"	Prion protein-interacting protein	ERI3	79033	ENSG00000117419			Eri3 (MGI:2153887)			
chr1	44405159	44651723	1p34.1	1p34.1		616136	RNF220	RING finger protein 220	RNF220	55182	ENSG00000187147			Rnf220 (MGI:1913993)			
chr1	44739703	44767766	1p34.1	1p34.1		604538	"KIF2C, KNSL6, MCAK"	"Kinesin family, member 2C"	KIF2C	11004	ENSG00000142945			Kif2c (MGI:1921054)			
chr1	44775573	44778739	1p34.1-p32	1p34.1		600357	RPS8	Ribosomal protein S8	RPS8	6202	ENSG00000142937			Rps8 (MGI:98166)			
chr1	44782144	44792827	1p33-p32.3	1p34.1		607336	"BEST4, VMD2L2"	Bestrophin 4	BEST4	266675	ENSG00000142959						
chr1	44799951	44805994	1p34.1	1p34.1		602913	"PLK3, CNK, PRK"	Polo-like kinase 3	PLK3	1263	ENSG00000173846	previously assigned to 8p21 by FISH		Plk3 (MGI:109604)			
chr1	44805907	44809751	1p34.1	1p34.1		611713	TCTEX1D4	TCTEX1 domain-containing 4	TCTEX1D4	343521	ENSG00000188396			Tctex1d4 (MGI:3045358)			
chr1	44819843	44842943	1p32	1p34.1		603673	PTCH2	"Patched, Drosophila, homolog of, 2"	PTCH2	8643	ENSG00000117425		"Basal cell carcinoma, somatic, 605462 (3); Basal cell nevus syndrome, 109400 (3), Autosomal dominant; Medulloblastoma, somatic, 155255 (3)"	Ptch2 (MGI:1095405)			
chr1	44850521	44986721	1p34.1	1p34.1		606273	EIF2B3	"Eukaryotic translation initiation factor 2B, subunit 3"	EIF2B3	8891	ENSG00000070785		"Leukoencephalopathy with vanishing white matter, 603896 (3), Autosomal recessive"	Eif2b3 (MGI:1313286)			
chr1	45012132	45015668	1p34	1p34.1		613521	UROD	Uroporphyrinogen decarboxylase	UROD	7389	ENSG00000126088		"Porphyria cutanea tarda, 176100 (3), Autosomal recessive, Autosomal dominant; Porphyria, hepatoerythropoietic, 176100 (3), Autosomal recessive, Autosomal dominant"	Urod (MGI:98916)			
chr1	45329241	45340469	1p34.3-p32.1	1p34.1		604933	"MUTYH, MYH"	"MutY, E. coli, homolog of"	MUTYH	4595	ENSG00000132781		"Adenomas, multiple colorectal, 608456 (3), Autosomal recessive; Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas, 132600 (3), Somatic mutation; Gastric cancer, somatic, 613659 (3)"	Mutyh (MGI:1917853)			
chr1	45339669	45343977	1p34.1	1p34.1		613931	"TOE1, PCH7"	Target of EGR1	TOE1	114034	ENSG00000132773		"Pontocerebellar hypoplasia, type 7, 614969 (3), Autosomal recessive"	Toe1 (MGI:1915526)			
chr1	45343882	45491341	1p32	1p34.1		604746	TESK2	Testis-specific protein kinase 2	TESK2	10420	ENSG00000070759			Tesk2 (MGI:2385204)			
chr1	45500183	45511265	1p34.1	1p34.1		609831	MMACHC	MMACHC gene	MMACHC	25974	ENSG00000132763		"Methylmalonic aciduria and homocystinuria, cblC type, 277400 (3), Autosomal recessive"	Mmachc (MGI:1914346)			
chr1	45511034	45522889	1p34.1	1p34.1		176763	"PRDX1, PRXI, PAGA, NKEFA"	Peroxiredoxin 1	PRDX1	5052	ENSG00000117450	pseudogene PAGB on 9p22	"Methylmalonic aciduria and homocystinuria, cblC type, digenic, 277400 (3), Autosomal recessive"	Prdx1 (MGI:99523)			
chr1	45550778	45570050	1p33-p32	1p34.1		103830	"AKR1A1, ALR"	"Aldo-keto reductase family 1, member A1 (aldehyde reductase)"	AKR1A1	10327	ENSG00000117448			Akr1a1 (MGI:1929955)			
chr1	45583987	45618905	1p34.1	1p34.1		603185	NASP	Nuclear autoantigenic sperm protein	NASP	4678	ENSG00000132780			Nasp (MGI:1355328)			
chr1	45694323	45750812	1p32-p22	1p34.1		147485	IPP	Intracisternal A particle-promoted polypeptide	IPP	3652	ENSG00000197429			Ipp (MGI:96581)			
chr1	45786991	46036123	1p34.1	1p34.1		612257	"MAST2, MAST205, KIAA0807"	Microtubule-associated serine/threonine kinase 2	MAST2	23139	ENSG00000086015			Mast2 (MGI:894676)			
chr1	46040139	46174900	1p34.2	1p34.1		606076	PIK3R3	"Phosphatidylinositol 3-kinase, regulatory, 3"	PIK3R3	8503	ENSG00000117461			Pik3r3 (MGI:109277)			
chr1	46175076	46196488	1p34.1	1p34.1		613170	"TSPAN1, NET1"	Tetraspanin 1	TSPAN1	10103	ENSG00000117472			Tspan1 (MGI:1914055)			
chr1	46188680	46220304	1p34-p33	1p34.1		606822	"POMGNT1, MEB, MDDGA3, MDDGB3, MDDGC3, RP76"	"Protein 0-mannose beta-1,2-N-acetylglucosaminyltransferase"	POMGNT1	55624	ENSG00000085998		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3, 253280 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3, 613151 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3, 613157 (3), Autosomal recessive; Retinitis pigmentosa 76, 617123 (3), Autosomal recessive"	Pomgnt1 (MGI:1915523)			
chr1	46203333	46221255	1p34.1	1p34.1		616129	"LURAP1, LRAP35A"	Leucine-rich adaptor protein 1	LURAP1	541468	ENSG00000171357			Lurap1 (MGI:1915325)			
chr1	46247694	46278476	1p32	1p34.1		603615	"RAD54L, HR54, HRAD54"	"RAD54, S. cerevisiae, homolog-like"	RAD54L	8438	ENSG00000085999		"Adenocarcinoma, colonic, somatic (3); {Breast cancer, invasive ductal}, 114480 (3), Autosomal dominant; Lymphoma, non-Hodgkin, somatic, 605027 (3)"	Rad54l (MGI:894697)			
chr1	46300000	60800000	1p33-p32			612728	BMND14	Bone mineral density quantitative trait locus 14		100294718		associated with rs17131547	"[Bone mineral density QTL 14], 612728 (2)"				
chr1	46300000	84400000	1p33-p31.1			613606	FWS	Forsythe-Wakeling syndrome		100529224		between rs2354462 and rs718883	"Forsythe-Wakeling syndrome, 613606 (2), Autosomal recessive"				
chr1	46300000	50200000	1p33			613857	OFC13	Orofacial cleft 13		100653367		associated with rs3827730	"Orofacial cleft 13, 613857 (2), Autosomal dominant"				
chr1	46300000	50200000	1p33			616392	"SKINTL, SKINTP"	SKINT1-like pseudogene	SKINT1L	391037							
chr1	46303612	46316776	1p34.1	1p33		613844	UQCRH	Ubiquinol-cytochrome c reductase hinge protein	UQCRH	7388	ENSG00000173660	pseudogene on 1p36		Uqcrh-ps1 (MGI:3641869)			
chr1	46340176	46365151	1p33	1p33		615394	NSUN4	"NOP2/SUN RNA methyltransferase family, member 4"	NSUN4	387338	ENSG00000117481			Nsun4 (MGI:1919431)			
chr1	46394266	46413847	1p33	1p33		602935	FAAH	Fatty acid amide hydrolase	FAAH	2166	ENSG00000117480		"{Drug addiction, susceptibility to}, 606581 (3)"	Faah (MGI:109609)			
chr1	46489836	46514225	1p33	1p33		607410	"DMBX1, OTX3"	Diencephalon/mesencephalon homeobox 1	DMBX1	127343	ENSG00000197587			Dmbx1 (MGI:2153518)			
chr1	46545637	46551656	1p33	1p33		611455	"KNCN, KINO, L5"	Kinocilin	KNCN	148930	ENSG00000162456			Kncn (MGI:3614952)			
chr1	46557406	46604310	1p33	1p33		606724	"MKNK1, MNK1"	Mitogen-activated protein kinase-interacting serine/threonine kinase 1	MKNK1	8569	ENSG00000079277			Mknk1 (MGI:894316)			
chr1	46798997	46819348	1p34-p12	1p33		124075	CYP4B1	"Cytochrome P450, subfamily IVB, polypeptide 1"	CYP4B1	1580	ENSG00000142973			Cyp4b1 (MGI:103225)			
chr1	46929173	46941483	1p33	1p33		601310	CYP4A11	"Cytochrome P450, subfamily IVA, polypeptide 11"	CYP4A11	1579	ENSG00000187048			"Cyp4a10,Cyp4a32,Cyp4a31 (MGI:88611,MGI:3717148,MGI:3028580)"			
chr1	46961363	47055431	1p33	1p33		614999	"CYP4X1, CYPIVX1"	"Cytochrome P450, family 4, subfamily X, polypeptide 1"	CYP4X1	260293	ENSG00000186377			Cyp4x1 (MGI:1932403)			
chr1	47137424	47149737	1p33	1p33		615341	CYP4A22	"Cytochrome P450, family 4, subfamily A, polypeptide 22"	CYP4A22	284541	ENSG00000162365			"Cyp4a12a,Cyp4a12b (MGI:3611747,MGI:88612)"			
chr1	47183588	47190098	1p33	1p33		607178	"PDZK1IP1, MAP17"	PDZK1-interacting protein 1	PDZK1IP1	10158	ENSG00000162366	"near SLC in human, mouse, chicken, zebrafish"		Pdzk1ip1 (MGI:1914432)			
chr1	47216289	47232388	1p32	1p33		187040	"TAL1, TCL5, SCL"	T-cell acute lymphocytic leukemia-1	TAL1	6886	ENSG00000162367	proximal to MYCL1	"Leukemia, T-cell acute lymphocytic, somatic, 613065 (3)"	Tal1 (MGI:98480)			
chr1	47250138	47314786	1p33	1p33		181590	"STIL, SIL, MCPH7"	SCL/TAL1-interrupting locus	STIL	6491	ENSG00000123473	within about 250kb of SCL	"Microcephaly 7, primary, autosomal recessive, 612703 (3), Autosomal recessive"	Stil (MGI:107477)			
chr1	47333796	47378838	1p32	1p33		191710	"CMPK1, CMPK, UMPK, UMK, CMK"	"Cytidine monophosphate (UMP-CMP) kinase 1, cytosolic"	CMPK1	51727	ENSG00000162368			Cmpk1 (MGI:1913838)			
chr1	47416071	47418051	1p32	1p33		601094	"FOXE3, FKHL12, ASMD, CTRCT34, ASGD2, AAT11"	Forkhead box E3	FOXE3	2301	ENSG00000186790		"Anterior segment dysgenesis 2, multiple subtypes, 610256 (3), Autosomal recessive; {Aortic aneurysm, familial thoracic 11, susceptibility to}, 617349 (3), Autosomal dominant; Cataract 34, multiple types, 612968 (3)"				
chr1	47436016	47440690	1p34-p32	1p33		602211	"FOXD2, FKHL17, FREAC9"	Forkhead box D2	FOXD2	2306	ENSG00000186564			Foxd2 (MGI:1347471)			
chr1	47760527	47997367	1p33	1p33		614913	"TRABD2B, TIKI2"	TRAB domain-containing protein 2B	TRABD2B	388630	ENSG00000269113			Trabd2b (MGI:3650152)			
chr1	48258642	48472207	1p33	1p33		613947	"SPATA6, SRF1, HASH"	Spermatogenesis-associated protein 6	SPATA6	54558	ENSG00000132122			Spata6 (MGI:1915196)			
chr1	48520156	50023953	1p33	1p33		616476	"AGBL4, CCP6"	ATP/GTP-binding protein-like 4	AGBL4	84871	ENSG00000186094			Agbl4 (MGI:1918244)			
chr1	50048013	50203785	1p34	1p33-p32		168360	"ELAVL4, HUD, PNEM"	"Embryonic lethal, abnormal vision, Drosophila, homolog of, like-4 (Hu antigen D)"	ELAVL4	1996	ENSG00000162374		"Neuropathy, paraneoplastic sensory (1)"	Elavl4 (MGI:107427)			
chr1	50200000	60800000	1p32			606852	"PARK10, AAOPD"	Parkinson disease 10	PARK10	170534		max lod at D1S2652; ?associated with CDCP2	"{Parkinson disease 10}, 606852 (2)"				
chr1	50200000	60800000	1p32			613548	STQTL23	Stature quantitative trait locus 23		100529222		linked to rs628667	"{Stature QTL 23}, 613548 (2)"				
chr1	50417549	50423446	1p33-p32.3	1p32.3		614804	DMRTA2	Doublesex- and MAB3-related transcription factor A2	DMRTA2	63950	ENSG00000142700			Dmrta2 (MGI:2653629)			
chr1	50441262	50960263	1p33	1p32.3		604460	"FAF1, HFAF1"	Fas-associated factor 1	FAF1	11124	ENSG00000185104			Faf1 (MGI:109419)			
chr1	50968694	50974636	1p32	1p32.3		603369	"CDKN2C, INK4C"	Cyclin-dependent kinase inhibitor 2C	CDKN2C	1031	ENSG00000123080			Cdkn2c (MGI:105388)			
chr1	51236272	51273446	1p32-p31	1p32.3		612598	RNF11	Ring finger protein 11	RNF11	26994	ENSG00000123091			Rnf11 (MGI:1352759)			
chr1	51354262	51519322	1p32	1p32.3		600051	EPS15	Epidermal growth factor receptor pathway substrate-15	EPS15	2060	ENSG00000085832			Eps15 (MGI:104583)			
chr1	51616873	51789218	1p34.2-p32.2	1p32.3		606737	"OSBPL9, ORP9"	Oxysterol-binding protein-like protein 9	OSBPL9	114883	ENSG00000117859			Osbpl9 (MGI:1923784)			
chr1	51789191	51878936	1p32.2	1p32.3		602651	NRD1	Nardilysin (N-arginine dibasic convertase)	NRDC	4898	ENSG00000078618			Nrd1 (MGI:1201386)			
chr1	51907955	51990763	1p32-p31	1p32.3		179510	RAB3B	Brain antigen RAB3B	RAB3B	5865	ENSG00000169213			Rab3b (MGI:1917158)			
chr1	52020130	52056170	1p32.3	1p32.3		609448	"TXNDC12, TLP19, ERP18"	Thioredoxin domain-containing protein 12	TXNDC12	51060	ENSG00000117862			Txndc12 (MGI:1913323)			
chr1	52142000	52348663	1p32.3	1p32.3		603755	"ZFYVE9, MADHIP, SARA"	"Zinc finger, FYVE domain containing 9"	ZFYVE9	9372	ENSG00000157077			Zfyve9 (MGI:2652838)			
chr1	52372828	52404470	1p32	1p32.3		601902	"ORC1, ORC1L"	"Origin recognition complex, subunit 1, S. cerevisiae, homolog"	ORC1	4998	ENSG00000085840		"Meier-Gorlin syndrome 1, 224690 (3), Autosomal recessive"	Orc1 (MGI:1328337)			
chr1	52404546	52418319	1p32.3	1p32.3		617031	"PRPF38A, PRP38A"	"Precursor mRNA-processing factor 38, S. cerevisiae, homolog of, A"	PRPF38A	84950	ENSG00000134748			Prpf38a (MGI:1916962)			
chr1	52423274	52553462	1q23.3	1p32.3		613692	"ZCCHC11, KIAA0191"	Zinc finger CCHC domain-containing protein 11	ZCCHC11	23318	ENSG00000134744			Zcchc11 (MGI:2445126)			
chr1	52602370	52609050	1p32	1p32.3		615784	"GPX7, NPGPX"	Glutathione peroxidase 7	GPX7	2882	ENSG00000116157			Gpx7 (MGI:1914555)			
chr1	52686341	52698365	1p32.3	1p32.3		615623	"COA7, RESA1, SELRC1, C1orf163"	Cytochrome C oxidase assembly factor	COA7	65260	ENSG00000162377	mutation identified in 1 COX4D patient	"?Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Coa7 (MGI:1917143)			
chr1	52927228	53051616	1p32	1p32.3		184755	SCP2	Sterol carrier protein-2	SCP2	6342	ENSG00000116171	mutation identified in 1 LKDMN patient	"?Leukoencephalopathy with dystonia and motor neuropathy, 613724 (3), Autosomal recessive"	Scp2 (MGI:98254)			
chr1	53062051	53085501	1p32.3	1p32.3		608661	PODN	Podocan	PODN	127435	ENSG00000174348			Podn (MGI:2674939)			
chr1	53196428	53214196	1p32	1p32.3		600650	"CPT2, IIAE4"	Carnitine palmitoyltransferase II	CPT2	1376	ENSG00000157184	formerly at 1p13	"CPT II deficiency, infantile, 600649 (3), Autosomal recessive; CPT II deficiency, lethal neonatal, 608836 (3), Autosomal recessive; CPT II deficiency, myopathic, stress-induced, 255110 (3), Autosomal recessive, Autosomal dominant; {Encephalopathy, acute, infection-induced, 4, susceptibility to}, 614212 (3), Autosomal recessive, Autosomal dominant"	Cpt2 (MGI:109176)			
chr1	53226891	53238609	1p34-p33	1p32.3		602603	MAGOH	"Mago nashi, Drosophila, homolog of, proliferation-associated"	MAGOH	4116	ENSG00000162385			Magoh (MGI:1330312)			
chr1	53242363	53328148	1p34	1p32.3		602600	"LRP8, APOER2, MCI1"	Low density lipoprotein receptor-related protein 8 (Apolipoprotein E receptor 2)	LRP8	7804	ENSG00000157193		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Lrp8 (MGI:1340044)			
chr1	53459398	53467487	1p32.2	1p32.3		614805	DMRTB1	Doublesex- and MAB3-related transcription factor B1	DMRTB1	63948	ENSG00000143006			Dmrtb1 (MGI:1927125)			
chr1	53506232	53739170	1p32.3	1p32.3		610378	GLIS1	Glis family zinc finger protein 1	GLIS1	148979	ENSG00000174332			Glis1 (MGI:2386723)			
chr1	53765459	53838551	1p32.3	1p32.3		610115	"TMEM48, NDC1"	Transmembrane protein 48	NDC1	55706	ENSG00000058804			Ndc1 (MGI:1920037)			
chr1	53851718	53889830	1p32.3	1p32.3		617521	YIPF1	"YIP1 domain family, member 1"	YIPF1	54432	ENSG00000058799			Yipf1 (MGI:1915532)			
chr1	53894186	53911085	1p33-p32	1p32.3		147892	"DIO1, TXDI1"	"Deiodinase, iodothyronine, type I"	DIO1	1733	ENSG00000211452			Dio1 (MGI:94896)			
chr1	54026680	54053572	1p32.3	1p32.3		617084	"TMEM59, DCF1"	Transmembrane protein 59	TMEM59	9528	ENSG00000116209			Tmem59 (MGI:1929278)			
chr1	54132719	54153180	1p32	1p32.3		612320	CDCP2	Cub domain-containing protein 2	CDCP2	200008	ENSG00000157211	?associated with PARK10		Cdcp2 (MGI:3045328)			
chr1	54200166	54225488	1p32.1	1p32.3		611843	MRPL37	Mitochondrial ribosomal protein L37	MRPL37	51253	ENSG00000116221			Mrpl37 (MGI:1926268)			
chr1	54225430	54413478	1p31.3	1p32.3		607390	SSBP3	Single-stranded DNA-binding protein 3	SSBP3	23648	ENSG00000157216			Ssbp3 (MGI:1919725)			
chr1	54548133	54634743	1p32.3	1p32.3		606803	"ACOT11, THEA, BFIT, BFIT1, BFIT2, KIAA0707"	Acyl-CoA thioesterase 11	ACOT11	26027	ENSG00000162390			Acot11 (MGI:1913736)			
chr1	54715821	54742656	1p31.3	1p32.3		606753	TTC4	Tetratricopeptide repeat domain 4	TTC4	7268	ENSG00000243725	pseudogene on 7p14-p13		Ttc4 (MGI:1919604)			
chr1	54756897	54764552	1p32.2	1p32.3		612036	PARS2	Prolyl-tRNA synthetase 2	PARS2	25973	ENSG00000162396			Pars2 (MGI:2386296)			
chr1	54806062	54842263	1p32.3	1p32.3		616446	"LEXM, C1orf177, LEM"	Lymphocyte expansion molecule	LEXM	163747	ENSG00000162398			Lexm (MGI:2681853)			
chr1	54849626	54887247	1p33-p31.1	1p32.3		606418	"DHCR24, KIAA0018"	24-dehydrocholesterol reductase	DHCR24	1718	ENSG00000116133		"Desmosterolosis, 602398 (3), Autosomal recessive"	Dhcr24 (MGI:1922004)			
chr1	54998943	55008791	1p31	1p32.3		606412	BSND	Barttin	BSND	7809	ENSG00000162399		"Bartter syndrome, type 4a, 602522 (3), Autosomal recessive; Sensorineural deafness with mild renal dysfunction, 602522 (3), Autosomal recessive"	Bsnd (MGI:2153465)			
chr1	55039475	55064852	1p32.3	1p32.3		607786	"PCSK9, NARC1, HCHOLA3, FH3, LDLCQ1"	"Proprotein convertase, subtilisin/kexin-type, 9"	PCSK9	255738	ENSG00000169174		"Hypercholesterolemia, familial, 3, 603776 (3); {Low density lipoprotein cholesterol level QTL 1}, 603776 (3)"	Pcsk9 (MGI:2140260)			
chr1	55066358	55215373	1p32.3	1p32.3		610569	"USP24, KIAA1057"	Ubiquitin-specific protease 24	USP24	23358	ENSG00000162402			Usp24 (MGI:1919936)			
chr1	56494746	56579583	1p32.2	1p32.2		607125	"PLPP3, PPAP2B"	Phospholipid phosphatase 3	PLPP3	8613	ENSG00000162407			Plpp3 (MGI:1915166)			
chr1	56645316	56715334	1p31	1p32.2		600497	"PRKAA2, AMPK"	"Protein kinase, AMP-activated, alpha-2 catalytic subunit"	PRKAA2	5563	ENSG00000162409			Prkaa2 (MGI:1336173)			
chr1	56854769	56918220	1p32	1p32.2		120950	C8A	"Complement component-8, alpha polypeptide"	C8A	731	ENSG00000157131		"C8 deficiency, type I, 613790 (3), Autosomal recessive"	C8a (MGI:2668347)			
chr1	56929209	56974382	1p32	1p32.2		120960	C8B	"Complement component-8, beta polypeptide"	C8B	732	ENSG00000021852		"C8 deficiency, type II, 613789 (3), Autosomal recessive"	C8b (MGI:88236)			
chr1	56994777	58250546	1p32-p31	1p32.2		603448	"DAB1, SCA37"	"Disabled, Drosophila, homolog 1"	DAB1	1600	ENSG00000173406		"Spinocerebellar ataxia 37, 615945 (3), Autosomal dominant"	Dab1 (MGI:108554)			
chr1	58480718	58546798	1p32.3-p32.1	1p32.2-p32.1		617081	"OMA1, MPRP1"	OMA1 zinc metallopeptidase	OMA1	115209	ENSG00000162600			Oma1 (MGI:1914263)			
chr1	58575422	58577493	1p32	1p32.1		137290	"TACSTD2, TROP2, M1S1"	Tumor-associated calcium signal transducer 2	TACSTD2	4070	ENSG00000184292		"Corneal dystrophy, gelatinous drop-like, 204870 (3), Autosomal recessive"	Tacstd2 (MGI:1861606)			
chr1	58654738	58700090	1p32.1	1p32.1		612176	"MYSM1, 2ADUB, KIAA1915"	"MYB-like, SWIRM, and MPN domains-containing protein 1"	MYSM1	114803	ENSG00000162601			Mysm1 (MGI:2444584)			
chr1	58780790	58784112	1p32-p31	1p32.1		165160	JUN	Avian sarcoma virus 17 (v-jun) oncogene homolog	JUN	3725	ENSG00000177606			Jun (MGI:96646)			
chr1	59296404	59762729	1p32.1	1p32.1		611370	"FGGY, FLJ10986"	FGGY carbohydrate kinase domain-containing protein	FGGY	55277	ENSG00000172456			Fggy (MGI:1922828)			
chr1	59814860	59876377	1p32.1	1p32.1		607820	"HOOK1, HK1"	"Hook, Drosophila, homolog of, 1"	HOOK1	51361	ENSG00000134709			Hook1 (MGI:1925213)			
chr1	59893307	59926797	1p31.3-p31.2	1p32.1		601258	CYP2J2	"Cytochrome P450, subfamily IIJ (arachidonic acid epoxygenase), polypeptide 2"	CYP2J2	1573	ENSG00000134716			Cyp2j6 (MGI:1270148)			
chr1	60800000	84400000	1p31			601676	AIR	Acute insulin response		7808			"Acute insulin response, 601676 (2)"				
chr1	60800000	84400000	1p31			610906	ASRT4	"Asthma-related traits, susceptibility to, 4"		100188823		max lod at D1S2890	"{Asthma-related traits, susceptibility to, 4}, 610906 (2)"				
chr1	60800000	106700000	1p31-p21			606215	"AVSD1, AVCD"	"Atrioventricular septal defect, susceptibility to, 1"	AVSD1	7446			"{Atrioventricular septal defect, susceptibility to, 1}, 606215 (2)"				
chr1	60800000	84400000	1p31			615892	OFC14	Orofacial cleft 14		103581096			"Orofacial cleft 14, 615892 (2), Autosomal recessive"				
chr1	60800000	68500000	1p31.3			164750	"OPHLC, C1DUPp31.3, DUP1p31.3"	Omphalocele due to duplication of 1p31.3				duplication of 710kb at 1p31.3	"Omphalocele due to duplication of 1p31.3, 164750 (4), Autosomal dominant"				
chr1	60800000	84400000	1p31			606787	PAOD1	Peripheral arterial occlusive disease 1		171513			"Peripheral arterial occlusive disease 1, 606787 (2)"				
chr1	60800000	84400000	1p31.3-p31.1			612293	"POROK5, DSAP3"	"Porokeratosis 5, disseminated superficial actinic"		100190982		between D1S438 and D1S464	"Porokeratosis 5, disseminated superficial actinic, 612293 (2)"				
chr1	61077256	61462787	1p31.3-p31.2	1p31.3		600727	"NFIA, BRMUTD"	Nuclear factor I/A	NFIA	4774	ENSG00000162599		"Brain malformations with or without urinary tract defects, 613735 (3), Isolated cases"	Nfia (MGI:108056)			
chr1	61681046	61725422	1p31.3	1p31.3		610080	"TM2D1, BBP"	TM2 domain-containing protein 1	TM2D1	83941	ENSG00000162604			Tm2d1 (MGI:2137022)			
chr1	61742465	62163919	1p31.3	1p31.3		603199	"INADL, PATJ"	"INAD, Drosophila, homolog of"	PATJ	10207	ENSG00000132849			Patj (MGI:1277960)			
chr1	62236164	62319413	1p31.3	1p31.3		614612	KANK4	KN motif- and ankyrin repeat domain-containing protein 4	KANK4	163782	ENSG00000132854			Kank4 (MGI:3043381)			
chr1	62436303	62451803	1p32.1-p31.3	1p31.3		603478	USP1	Ubiquitin-specific protease 1	USP1	7398	ENSG00000162607			Usp1 (MGI:2385198)			
chr1	62454725	62688367	1p31.3	1p31.3		615730	"DOCK7, KIAA1771, EIEE23"	Dedicator of cytokinesis 7	DOCK7	85440	ENSG00000116641		"Epileptic encephalopathy, early infantile, 23, 615859 (3), Autosomal recessive"	Dock7 (MGI:1914549)			
chr1	62597486	62606304	1p31	1p31.3		604774	"ANGPTL3, ANGPT5, FHBL2"	Angiopoietin-like 3	ANGPTL3	27329	ENSG00000132855		"Hypobetalipoproteinemia, familial, 2, 605019 (3), Autosomal recessive"	Angptl3 (MGI:1353627)			
chr1	62783764	62865269	1p31.3	1p31.3		611339	"ATG4C, APG4C"	"Autophagy 4, S. cerevisiae, homolog of, C"	ATG4C	84938	ENSG00000125703			Atg4c (MGI:2651854)			
chr1	63323058	63325125	1p31	1p31.3		611539	"FOXD3, AIS1, VAMAS2"	Forkhead box D3	FOXD3	27022	ENSG00000187140		"{Autoimmune disease, susceptibility to, 1}, 607836 (3), Autosomal dominant"	Foxd3 (MGI:1347473)			
chr1	63367589	63438561	1p22.3	1p31.3		604566	"ALG6, CDG1C"	"Alg6, S. cerevisiae, homolog of"	ALG6	29929	ENSG00000088035		"Congenital disorder of glycosylation, type Ic, 603147 (3), Autosomal recessive"	Alg6 (MGI:2444031)			
chr1	63440769	63529394	1p31.3	1p31.3		605494	"ITGB3BP, NRIF3"	"Integrin, beta-3, binding protein of"	ITGB3BP	23421	ENSG00000142856			Itgb3bp (MGI:1914983)			
chr1	63523300	63585400	1p31.3	1p31.3		617632	"EFCAB7, KIAA1799"	EF-hand calcium-binding domain-containing protein 7	EFCAB7	84455	ENSG00000203965			Efcab7 (MGI:2385199)			
chr1	63593275	63660244	1p31	1p31.3		171900	"PGM1, GSD14, CDG1T"	Phosphoglucomutase-1	PGM1	5236	ENSG00000079739	distal to ACADM; formerly 1p22.1	"Congenital disorder of glycosylation, type It, 614921 (3), Autosomal recessive"	Pgm2 (MGI:97565)			
chr1	63774018	64181497	1p31.3	1p31.3		602336	"ROR1, NTRKR1"	Receptor tyrosine kinase-like orphan receptor 1	ROR1	4919	ENSG00000185483	mutation identified in 1 DFNB108 family	"?Deafness, autosomal recessive 108, 617654 (3), Autosomal recessive"	Ror1 (MGI:1347520)			
chr1	64744978	64833410	1p31.3	1p31.3		609953	"RAVER2, KIAA1579"	"Raver2, mouse, homolog of"	RAVER2	55225	ENSG00000162437			Raver2 (MGI:2443623)			
chr1	64833222	65067745	1p31.3	1p31.3		147795	JAK1	Janus kinase 1 (a protein-tyrosine kinase)	JAK1	3716	ENSG00000162434	related gene on 9p24		Jak1 (MGI:96628)			
chr1	65058433	65058507	1p31.3	1p31.3		612511	"MIR101-1, MIRN101-1"	Micro RNA 101-1	MIR101-1	406893		"another locus, MIRN101-2, on 9p24"					
chr1	65147341	65232144	1p31.3	1p31.3		103030	AK3	"Adenylate kinase-3, mitochondrial"	AK4	205	ENSG00000162433			Ak4 (MGI:87979)			
chr1	65264693	65415868	1p32.1-p31.3	1p31.3		608375	"DNAJC6, DJC6, KIAA0473, PARK19"	"DNAJ, E. coli, homolog of, subfamily C, member 6"	DNAJC6	9829	ENSG00000116675		"Parkinson disease 19a, juvenile-onset, 615528 (3), Autosomal recessive; Parkinson disease 19b, early-onset, 615528 (3), Autosomal recessive"	Dnajc6 (MGI:1919935)			
chr1	65420447	65436006	1p31	1p31.3		613461	"LEPROT, OBRGRP"	Leptin receptor overlapping transcript	LEPROT	54741	ENSG00000213625	transcribed in same direction as LEPR		Leprot (MGI:2687005)			
chr1	65420651	65637492	1p31	1p31.3		601007	"LEPR, OBR, LEPRD"	Leptin receptor	LEPR	3953	ENSG00000116678		"Obesity, morbid, due to leptin receptor deficiency, 614963 (3)"	Lepr (MGI:104993)			
chr1	65792509	66374578	1p31	1p31.3		600127	"PDE4B, DPDE4"	"Phosphodiesterase-4B, cAMP-specific (dunce-like phosphodiesterase E4)"	PDE4B	5142	ENSG00000184588			Pde4b (MGI:99557)			
chr1	66533271	66751138	1p31.3	1p31.3		611540	SGIP1	SH3-domain GRB2-like (endophilin)-interacting protein 1	SGIP1	84251	ENSG00000118473			Sgip1 (MGI:1920344)			
chr1	66797740	66801258	1p31.1-p22.3	1p31.3		606413	INSL5	Insulin-like 5	INSL5	10022	ENSG00000172410			Insl5 (MGI:1346085)			
chr1	66924894	66988618	1p31.3	1p31.3		616848	"MEIR1, KIAA1610"	Mesoderm induction-early response protein 1	MIER1	57708	ENSG00000198160			Mier1 (MGI:1918398)			
chr1	66999331	67054422	1p32-p31	1p31.3		610804	"SLC35D1, UGTREL7, KIAA0260, SHNKND"	"Solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1"	SLC35D1	23169	ENSG00000116704		"Schneckenbecken dysplasia, 269250 (3), Autosomal recessive"	Slc35d1 (MGI:2140361)			
chr1	67138638	67259978	1p31.3	1p31.3		607562	"IL23R, IBD17"	Interleukin 23 receptor	IL23R	149233	ENSG00000162594		"{Inflammatory bowel disease 17, protection against}, 612261 (3); {Psoriasis, protection against}, 605606 (3)"	Il23r (MGI:2181693)			
chr1	67307350	67397729	1p31.2	1p31.3		601642	IL12RB2	"Interleukin 12 receptor, beta-2"	IL12RB2	3595	ENSG00000081985			Il12rb2 (MGI:1270861)			
chr1	67407809	67430439	1p31.3	1p31.3		607378	"SERBP1, PAIRBP1"	Serpine1 mRNA-binding protein 1	SERBP1	26135	ENSG00000142864			Serbp1 (MGI:1914120)			
chr1	67685176	67688337	1p34-p12	1p31.3		126335	"DDIT1, GADD45"	DNA damage-inducible transcript-1	GADD45A	1647	ENSG00000116717			Gadd45a (MGI:107799)			
chr1	67701465	67833471	1p31.3	1p31.3		615405	GNG12	"Guanine nucleotide-binding protein, gamma 12"	GNG12	55970	ENSG00000172380			Gng12 (MGI:1336171)			
chr1	67832287	68202986	1p31.3	1p31.3		615406	GNG12AS1	GNG12 antisense RNA 1	GNG12-AS1	100289178							
chr1	68045961	68051630	1p31.3	1p31.3		605193	"DIRAS3, ARHI"	"DIRAS family, GTP-binding RAS-like protein 3"	DIRAS3	9077	ENSG00000162595						
chr1	68098458	68233017	1p31.3	1p31.3		611514	"WLS, GPR177, EVI"	"WNTless, Drosophila, homolog of"	WLS	79971	ENSG00000116729			Wls (MGI:1915401)			
chr1	68428821	68450321	1p31	1p31.3		180069	"RPE65, RP20, LCA2"	"Retinal pigment epithelium-specific protein, 65kD"	RPE65	6121	ENSG00000116745		"Leber congenital amaurosis 2, 204100 (3), Autosomal recessive; Retinitis pigmentosa 20, 613794 (3), Autosomal recessive"	Rpe65 (MGI:98001)			
chr1	68474151	68497220	1p31.2	1p31.3		612002	DEPDC1	DEP domain-containing 1	DEPDC1	55635	ENSG00000024526			Depdc1a (MGI:1923381)			
chr1	68500000	69300000	1p31.2			613008	PBC3	"Biliary cirrhosis, primary, 3"		100303717		associated with rs3790567	"{Biliary cirrhosis, primary, 3}, 613008 (2)"				
chr1	69300000	106700000	1p31.1-p21.1			609727	SPG29	"Spastic paraplegia 29, autosomal dominant"	SPG29	619379		max lod at D1S2865	"Spastic paraplegia 29, autosomal dominant, 609727 (2), Autosomal dominant"				
chr1	69567129	70152425	1p31.1	1p31.1		614453	"LRRC7, DENSIN, KIAA1365"	Leucine-rich repeat-containing protein 7	LRRC7	57554	ENSG00000033122			Lrrc7 (MGI:2676665)			
chr1	69919321	69920316	1p31	1p31.1		602051	PIN1L	"Peptidyl-prolyl cis/trans isomerase, NIMA-interacting-like"	PIN1P1	5301		?transcribed pseudogene					
chr1	70205681	70253051	1p31.1	1p31.1		602010	"SRSF11, SFRS11"	"Splicing factor, serine/arginine-rich, 11"	SRSF11	9295	ENSG00000116754			Srsf11 (MGI:1916457)			
chr1	70259001	70354976	1p31.1	1p31.1		615125	ANKRD13C	Ankyrin repeat domain-containing protein 13C	ANKRD13C	81573	ENSG00000118454			Ankrd13c (MGI:2139746)			
chr1	70353838	70368022	1p31.1	1p31.1		604372	HHLA3	Human endogenous retrovirus-H long terminal repeat-associating 3	HHLA3	11147	ENSG00000197568						
chr1	70411217	70441948	1p31.1	1p31.1		607657	CTH	Cystathionine gamma-lyase	CTH	1491	ENSG00000116761	previously assigned to chr.16	"Cystathioninuria, 219500 (3), Autosomal recessive; Homocysteine, total plasma, elevated (3)"	Cth (MGI:1339968)			
chr1	70852352	71047807	1p31.2	1p31.1		176806	"PTGER3, EP3"	"Prostaglandin E receptor 3, EP3 subtype"	PTGER3	5733	ENSG00000050628			Ptger3 (MGI:97795)			
chr1	71063290	71081288	1p22.1-p21.3	1p31.1		604347	"ZRANB2, ZNF265, ZIS"	Zinc finger RANBP2-type domain-containing protein 2	ZRANB2	9406	ENSG00000132485						
chr1	71402941	72282593	1p31.1	1p31.1		613173	"NEGR1, KILON"	Neuronal growth regulator 1	NEGR1	257194	ENSG00000172260			Negr1 (MGI:2444846)			
chr1	74198211	74208701	1p31.1	1p31.1		603609	"FPGT, GFPP"	Fucose-1-phosphate guanylyltransferase	FPGT	8790	ENSG00000254685			Fpgt (MGI:1922790)			
chr1	74235386	74544431	1p31.1	1p31.1		613932	"TNNI3K, CCDD"	TNNI3-interacting kinase	TNNI3K	51086	ENSG00000116783	mutation identified in 1 CCDD family	"?Cardiac conduction disease with or without dilated cardiomyopathy, 616117 (3), Autosomal dominant"	Tnni3k (MGI:2443276)			
chr1	74705469	74733407	1p31-p22	1p31.1		123691	CRYZ	"Crystallin, zeta (quinone reductase)"	CRYZ	1429	ENSG00000116791			Cryz (MGI:88527)			
chr1	74733151	74766676	1p31.3	1p31.1		611245	TYW3	"tRNA-wybutosine-synthesizing protein 3, S. cerevisiae, homolog of"	TYW3	127253	ENSG00000162623			Tyw3 (MGI:2445040)			
chr1	75128433	75199453	1p31.1	1p31.1		604425	LHX8	LIM homeobox 8	LHX8	431707	ENSG00000162624			Lhx8 (MGI:1096343)			
chr1	75724346	75763678	1p31	1p31.1		607008	"ACADM, MCAD"	"Acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain"	ACADM	34	ENSG00000117054		"Acyl-CoA dehydrogenase, medium chain, deficiency of, 201450 (3), Autosomal recessive"	Acadm (MGI:87867)			
chr1	75786193	75795089	1p31	1p31.1		179080	RABGGTB	"Rab geranylgeranyltransferase, beta subunit"	RABGGTB	5876	ENSG00000137955			Rabggtb (MGI:99537)			
chr1	75796870	75913237	1p31	1p31.1		602105	MSH4	"mutS, E. coli, homolog of, 4"	MSH4	4438	ENSG00000057468			Msh4 (MGI:1860077)			
chr1	76074683	76637315	1p31.1	1p31.1		610133	"ST6GALNAC3, SIAT7C"	"ST6 alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3"	ST6GALNAC3	256435	ENSG00000184005			St6galnac3 (MGI:1341828)			
chr1	76867407	77069166	1p31.1	1p31.1		610134	"ST6GALNAC5, SIAT7E"	"ST6 alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetylgalactosaminide alpha-2,6 sialyltransferase 5"	ST6GALNAC5	81849	ENSG00000117069			St6galnac5 (MGI:1349471)			
chr1	77088980	77219446	1p31.1	1p31.1		605087	"PIGK, GPI8"	"Phosphatidylinositol glycan, class K"	PIGK	10026	ENSG00000142892			Pigk (MGI:1913863)			
chr1	77281907	77559968	1p31	1p31.1		608009	AK5	Adenylate kinase 5	AK5	26289	ENSG00000154027			Ak5 (MGI:2677491)			
chr1	77695986	77759878	1p31.1	1p31.1		615146	"USP33, VDU1"	Ubiquitin-specific protease 33	USP33	23032	ENSG00000077254			Usp33 (MGI:2159711)			
chr1	77779623	77879539	1p31.1	1p31.1		616773	"FAM73A, MIGA1"	"Miga, Drosophila, homolog of, 1"	MIGA1	374986	ENSG00000180488			Miga1 (MGI:1924567)			
chr1	77888514	77948642	1p32-p31	1p31.1		613121	"NEXN, NELIN, CMD1CC, CMH20"	"Nexilin, rat, homolog of"	NEXN	91624	ENSG00000162614		"Cardiomyopathy, dilated, 1CC, 613122 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 20, 613876 (3), Autosomal dominant"	Nexn (MGI:1916060)			
chr1	77944050	77979434	1p31.1	1p31.1		603444	"FUBP1, FUBP, FBP"	Far upstream element-binding protein 1	FUBP1	8880	ENSG00000162613			Fubp1 (MGI:1196294)			
chr1	77979157	78017963	1p31.1	1p31.1		611327	"DNAJB4, HLJ1"	"DNAJ/HSP40 homolog, subfamily B, member 4"	DNAJB4	11080	ENSG00000162616			Dnajb4 (MGI:1914285)			
chr1	78490973	78540700	1p31.1	1p31.1		600563	PTGFR	Prostaglandin F receptor (FP)	PTGFR	5737	ENSG00000122420			Ptgfr (MGI:97796)			
chr1	78620381	78646144	1p31.1	1p31.1		613975	IFI44L	Interferon-induced protein 44-like	IFI44L	10964	ENSG00000137959			Ifi44l (MGI:95975)			
chr1	78648942	78664077	1p31.1	1p31.1		610468	"IFI44, P44"	Interferon-induced protein 44	IFI44	10561	ENSG00000137965			Ifi44 (MGI:2443016)			
chr1	78889763	79006809	1p31.1	1p31.1		616419	"ADGRL4, ETL, ELTD1"	Adhesion G protein-coupled receptor L4	ADGRL4	64123	ENSG00000162618			Adgrl4 (MGI:2655562)			
chr1	81306103	81993931	1p31.1	1p31.1		607018	"ADGRL2, LPHN2, LPHH1, CIRL2, CL2, KIAA0786"	Adhesion G protein-coupled receptor L2	ADGRL2	23266	ENSG00000117114			Adgrl2 (MGI:2139714)			
chr1	84077974	84238497	1p31.1	1p31.1		176892	PRKACB	"Protein kinase, cAMP-dependent, catalytic, beta"	PRKACB	5567	ENSG00000142875			Prkacb (MGI:97594)			
chr1	84398531	84415894	1p22.3	1p31.1-p22.3		608057	"DNASE2B, DLAD"	Deoxyribonuclease II beta	DNASE2B	58511	ENSG00000137976			Dnase2b (MGI:1913283)			
chr1	84400000	94300000	1p22			608035	CMM4	"Melanoma, cutaneous malignant, 4"		474388		between D1S430 and D1S2664	"{Melanoma, cutaneous malignant, 4}, 608035 (2)"				
chr1	84400000	94300000	1p22			611381	KAZA2	"Kala-azar, susceptibility to, 2"		101241898			"{Kala-azar, susceptibility to, 2}, 611381 (2)"				
chr1	84400000	94300000	1p22			191540	UOX	"Urate oxidase, pseudogene"	UOX	391051		nonsense mutations responsible for absence of enzyme in man and hominoid primates	[Urate oxidase deficiency] (1)				
chr1	84498322	84506578	1p22	1p22.3		600874	GNG5	"Guanine nucleotide-binding protein (G protein), gamma 5"	GNG5	2787	ENSG00000174021			"Gng5,Gng5-ps (MGI:3783217,MGI:109164)"			
chr1	84553120	84574479	1p22	1p22.3		600873	"CTBS, CTB"	"Chitobiase, di-N-acetyl-"	CTBS	1486	ENSG00000117151			Ctbs (MGI:1921495)			
chr1	84811600	84893212	1p31.1-p22.3	1p22.3		605106	"LPAR3, EDG7, LPA3"	Lysophosphatidic acid receptor 3	LPAR3	23566	ENSG00000171517			Lpar3 (MGI:1929469)			
chr1	84925582	84997121	1p22	1p22.3		607399	MCOLN2	Mucolipin 2	MCOLN2	255231	ENSG00000153898	incorrectly assigned to chr.3		Mcoln2 (MGI:1915529)			
chr1	85018081	85048901	1p22.3	1p22.3		607400	MCOLN3	Mucolipin 3	MCOLN3	55283	ENSG00000055732			Mcoln3 (MGI:1890500)			
chr1	85265775	85276903	1p22	1p22.3		603517	"BCL10, IMD37"	B-cell leukemia/lymphoma 10	BCL10	8915	ENSG00000142867	mutation identified in 1 IMD37 patient	"?Immunodeficiency 37, 616098 (3), Autosomal recessive; Lymphoma, MALT, somatic, 137245 (3); {Lymphoma, follicular, somatic}, 605027 (3); {Male germ cell tumor, somatic},, 273300 (3); {Mesothelioma, somatic}, 156240 (3); {Sezary syndrome, somatic} (3)"	Bcl10 (MGI:1337994)			
chr1	85318484	85578362	1p22	1p22.3		604743	DDAH1	Dimethylarginine dimethylaminohydrolase-1	DDAH1	23576	ENSG00000153904			Ddah1 (MGI:1916469)			
chr1	85580760	85583966	1p22.3	1p22.3		602369	"CYR61, IGFBP10"	"Cysteine-rich angiogenic inducer, 61 (insulin-like growth factor-binding protein-10)"	CYR61	3491	ENSG00000142871			Cyr61 (MGI:88613)			
chr1	85728506	86157035	1p22.3	1p22.3		610025	COL24A1	"Collagen, type XXIV, alpha-1"	COL24A1	255631	ENSG00000171502			Col24a1 (MGI:1918605)			
chr1	86423882	86456557	1p22.3	1p22.3		604003	CLCA2	Chloride channel accessory 2	CLCA2	9635	ENSG00000137975			Clca2 (MGI:2139758)			
chr1	86468842	86500293	1p22.3	1p22.3		603906	"CLCA1, CACC1"	Chloride channel accessory 1	CLCA1	1179	ENSG00000016490			Clca1 (MGI:1346342)			
chr1	86547075	86580757	1p22.3	1p22.3		616857	"CLCA4, CACC2"	Chloride channel accessory 4	CLCA4	22802	ENSG00000016602			"Clca4b,Clca4a (MGI:2139790,MGI:2139744)"			
chr1	86634275	86655375	1p22.32	1p22.3		604337	CLCA3	Chloride channel accessory 3	CLCA3P	9629							
chr1	86862444	86914576	1p31	1p22.3		606254	"SELENOF, SEP15"	Selenoprotein F	SELENOF	9403	ENSG00000183291			Selenof (MGI:1927947)			
chr1	86914651	87109997	1p22	1p22.3		604844	HS2ST1	Heparan sulfate 2-O-sulfotransferase 1	HS2ST1	9653	ENSG00000153936			Hs2st1 (MGI:1346049)			
chr1	87328467	87348922	1p22.3	1p22.3		603129	LMO4	LIM domain only 4	LMO4	8543	ENSG00000143013			Lmo4 (MGI:109360)			
chr1	88684143	88836254	1p22.2	1p22.2		602549	"PKN2, PRKCL2, PRK2, PAK2"	Protein kinase N2	PKN2	5586	ENSG00000065243			Pkn2 (MGI:109211)			
chr1	88852637	88891943	1p22.2	1p22.2		189963	"GTF2B, TFIIB, TF2B"	General transcription factor IIb	GTF2B	2959	ENSG00000137947			Gtf2b (MGI:2385191)			
chr1	88921043	88992959	1p22.2	1p22.2		610656	"CCBL2, KAT3"	Cysteine conjugate beta-lyase 2	KYAT3	56267	ENSG00000137944			Kyat3 (MGI:2677849)			
chr1	89006676	89022869	1p22.2	1p22.2		600413	GBP3	Guanylate-binding protein 3	GBP3	2635	ENSG00000117226			Gbp2b (MGI:95666)			
chr1	89052303	89065359	1p22.2	1p22.2		600411	GBP1	"Guanylate binding protein 1, interferon-inducible, 67kD"	GBP1	2633	ENSG00000117228						
chr1	89106131	89126158	1p22.2	1p22.2		600412	GBP2	"Guanylate-binding protein 2, interferon-inducible"	GBP2	2634	ENSG00000162645			Gbp2 (MGI:102772)			
chr1	89131750	89176039	1p22.2	1p22.2		612468	GBP7	Guanylate-binding protein 7	GBP7	388646	ENSG00000213512			Gbp7 (MGI:2444421)			
chr1	89181147	89198949	1p22.2	1p22.2		612466	GBP4	Guanylate-binding protein 4	GBP4	115361	ENSG00000162654			Gbp3 (MGI:1926263)			
chr1	89258949	89272860	1p22.2	1p22.2		611467	GBP5	Guanylate-binding protein 5	GBP5	115362	ENSG00000154451			Gbp5 (MGI:2429943)			
chr1	89363876	89388159	1p22.2	1p22.2		612467	GBP6	Guanylate-binding protein 6	GBP6	163351	ENSG00000183347			"Gbp6,Gbp10,Gbp11,Gbp9,Gbp4 (MGI:3605620,MGI:3646307,MGI:97072,MGI:4359647,MGI:2140937)"			
chr1	89522625	89597860	1p22.2	1p22.2		612888	"LRRC8B, TALRRP, KIAA0231"	Leucine-rich repeat-containing protein 8B	LRRC8B	23507	ENSG00000197147			Lrrc8b (MGI:2141353)			
chr1	89615809	89719534	1p22.2	1p22.2		612889	"LRRC8C, FAD158, AD158"	Leucine-rich repeat-containing protein 8C	LRRC8C	84230	ENSG00000171488			Lrrc8c (MGI:2140839)			
chr1	89821013	89936431	1p22.2	1p22.2		612890	"LRRC8D, LRRC5"	Leucine-rich repeat-containing protein 8D	LRRC8D	55144	ENSG00000171492			Lrrc8d (MGI:1922368)			
chr1	89995094	90035530	1p22.2	1p22.2		614601	"ZNF326, ZIRD"	Zinc finger protein 326	ZNF326	284695	ENSG00000162664			Zfp326 (MGI:1927246)			
chr1	90712021	90717236	1p22.3	1p22.2		605212	BARHL2	BARH-like 2	BARHL2	343472	ENSG00000143032			Barhl2 (MGI:1859314)			
chr1	90915297	91022266	1p22.2	1p22.2		614159	"ZNF644, MYP21"	Zinc finger protein 644	ZNF644	84146	ENSG00000122482		"Myopia 21, autosomal dominant, 614167 (3), Autosomal dominant"	Zfp644 (MGI:1277212)			
chr1	91260765	91408007	1p22.2	1p22.2		615684	"HFM1, MER3, POF9"	"Hfm1, ATP-dependent DNA helicase, S. cerevisiae, homolog of"	HFM1	164045	ENSG00000162669		"Premature ovarian failure 9, 615724 (3), Autosomal recessive"	Hfm1 (MGI:3036246)			
chr1	91498967	91525763	1p22	1p22.2-p22.1		603311	"CDC7L1, CDC7"	"Cell division cycle 7, S. Cerevisiae, homolog-like 1"	CDC7	8317	ENSG00000097046			Cdc7 (MGI:1309511)			
chr1	91500000	111200000	1p22.1-p13.3			608653	DFNB32	"Deafness, autosomal recessive 32"	DFNB32	113877		max lod at D1S21401	"Deafness, autosomal recessive 32, 608653 (2), Autosomal recessive"				
chr1	91680342	91906001	1p33-p32	1p22.1		600742	TGFBR3	"Transforming growth factor, beta receptor III (betaglycan, 300kD)"	TGFBR3	7049	ENSG00000069702			Tgfbr3 (MGI:104637)			
chr1	91949370	92014427	1p22.1	1p22.1		602144	"BRDT, SPGF21"	"Bromodomain, testis-specific"	BRDT	676	ENSG00000137948	mutation identified in 1 SPGF21 patient	"?Spermatogenic failure 21, 617644 (3), Autosomal recessive"	Brdt (MGI:1891374)			
chr1	92029975	92063535	1p22.1	1p22.1		617401	"EPHX4, ABHD7"	Epoxide hydrolase 4	EPHX4	253152	ENSG00000172031			Ephx4 (MGI:2686228)			
chr1	92245785	92441935	1p22-p21	1p22.1		601749	"GLML, GVM, VMGLOM"	Glomulin	GLMN	11146	ENSG00000174842		"Glomuvenous malformations, 138000 (3), Autosomal dominant"	Glmn (MGI:2141180)			
chr1	92298964	92388174	1p22.1	1p22.1		611476	"RPAP2, C1orf82"	RNA polymerase II-associated protein 2	RPAP2	79871	ENSG00000122484			Rpap2 (MGI:2141142)			
chr1	92473042	92486875	1p22	1p22.1		600871	"GFI1, ZNF163, SCN2"	Growth factor independent 1	GFI1	2672	ENSG00000162676	mutation identified in 1 SCN2 patient and 1 NICINA patient	"?Neutropenia, nonimmune chronic idiopathic, of adults, 607847 (3), Autosomal dominant; ?Neutropenia, severe congenital 2, autosomal dominant, 613107 (3), Autosomal dominant"	Gfi1 (MGI:103170)			
chr1	92508695	92792412	1p22	1p22.1		602942	"EVI5, NB4S"	Ecotropic viral integration site 5	EVI5	7813	ENSG00000067208			Evi5 (MGI:104736)			
chr1	92831985	92841923	1p22.1	1p22.1		603634	"RPL5, DBA6"	Ribosomal protein L5	RPL5	6125	ENSG00000122406		"Diamond-Blackfan anemia 6, 612561 (3), Autosomal dominant"	Rpl5 (MGI:102854)			
chr1	92832728	92961521	1p22.1	1p22.1		614542	FAM69A	"Family with sequence similarity 69, member A"	FAM69A	388650	ENSG00000154511			Fam69a (MGI:1914516)			
chr1	93079218	93139080	1p22.1	1p22.1		609882	"MTF2, PCL2, M96"	Metal-regulatory transcription factor 2	MTF2	22823	ENSG00000143033			Mtf2 (MGI:105050)			
chr1	93149741	93180688	1p22.1	1p22.1		616876	TMED5	Transmembrane p24 trafficking protein 5	TMED5	50999	ENSG00000117500			Tmed5 (MGI:1921586)			
chr1	93345920	93362591	1p22.1	1p22.1		601482	DR1	"Down-regulator of transcription 1, TBP-binding (negative cofactor 2)"	DR1	1810	ENSG00000117505			Dr1 (MGI:1100515)			
chr1	93448066	93569670	1p22.1	1p22.1		608848	"FNBP1L, TOCA1, C1orf39"	Formin binding protein 1-like	FNBP1L	54874	ENSG00000137942						
chr1	93561740	93847149	1p22.1	1p22.1		604704	"BCAR3, SH2D3B, NSP2"	Breast cancer antiestrogen resistance 3	BCAR3	8412	ENSG00000137936			Bcar3 (MGI:1352501)			
chr1	93869457	93879205	1p22.1	1p22.1		611199	"DNTTIP2, ERBP, FCF2"	DNTT-interacting protein 2	DNTTIP2	30836	ENSG00000067334			Dnttip2 (MGI:1923173)			
chr1	93885198	93910369	1p22.1	1p22.1		601176	"GCLM, GLCLR"	"Glutamate-cysteine ligase, modifier subunit"	GCLM	2730	ENSG00000023909		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Gclm (MGI:104995)			
chr1	93992836	94121148	1p22.1	1p22.1		601691	"ABCA4, ABCR, STGD1, FFM, RP19, CORD3, ARMD2"	"ATP-binding transporter, retina-specific"	ABCA4	24	ENSG00000198691		"Cone-rod dystrophy 3, 604116 (3); Fundus flavimaculatus, 248200 (3), Autosomal recessive; {Macular degeneration, age-related, 2}, 153800 (3), Autosomal dominant; Retinal dystrophy, early-onset severe, 248200 (3), Autosomal recessive; Retinitis pigmentosa 19, 601718 (3), Autosomal recessive; Stargardt disease 1, 248200 (3), Autosomal recessive"	Abca4 (MGI:109424)			
chr1	94168906	94275067	1p22.1	1p22.1		610496	"ARHGAP29, PARG1"	RHO GTPase-activating protein 29	ARHGAP29	9411	ENSG00000137962			Arhgap29 (MGI:2443818)			
chr1	94300000	111200000	1p21.3-p13.3			609913	RP32	Retinitis pigmentosa-32	RP32	641433		max lod at D1S485	"Retinitis pigmentosa 32, 609913 (2)"				
chr1	94300000	106700000	1p21			609822	STQTL7	Stature quantitative trait locus 7		100037265		max lod at D1S1631	"{Stature QTL 7}, 609822 (2)"				
chr1	94300000	111200000	1p21-p13.3			600193	WS2B	"Waardenburg syndrome, type 2B"	WS2B	7488			"Waardenburg syndrome, type 2B, 600193 (2), Autosomal dominant"				
chr1	94418085	94518662	1p22-p21	1p21.3		170995	"ABCD3, PXMP1, PMP70, CBAS5"	"ATP-binding cassette, subfamily D, member 3 (peroxisomal membrane protein 1, 70kD)"	ABCD3	5825	ENSG00000117528	mutation identified in 1 CBAS5 family	"?Bile acid synthesis defect, congenital, 5, 616278 (3), Autosomal recessive"	Abcd3 (MGI:1349216)			
chr1	94529175	94541856	1p22-p21	1p21.3		134390	"F3, TFA"	Coagulation factor III	F3	2152	ENSG00000117525			F3 (MGI:88381)			
chr1	94896948	94927222	1p22-p21	1p21.3		602374	CNN3	"Calponin 3, acidic"	CNN3	1266	ENSG00000117519			Cnn3 (MGI:1919244)			
chr1	94981564	95072973	1p21.3	1p21.3		612866	"ALG14, CMS15"	"Alg14, S. cerevisiae, homolog of"	ALG14	199857	ENSG00000172339	mutation identified in 1 CMSWTA family	"?Myasthenic syndrome, congenital, 15, without tubular aggregates, 616227 (3)"	Alg14 (MGI:1914039)			
chr1	95234154	95247224	1p21.3	1p21.3		615875	"RWDD3, RSUME"	RWD domain-containing protein 3	RWDD3	25950	ENSG00000122481			Rwdd3 (MGI:1920420)			
chr1	96721604	96815048	1p21	1p21.3		608449	"PTBP2, NPTB"	Polypyrimidine tract-binding protein 2	PTBP2	58155	ENSG00000117569			Ptbp2 (MGI:1860489)			
chr1	97077742	97921058	1p22	1p21.3		612779	"DPYD, DPD"	Dihydropyrimidine dehydrogenase	DPYD	1806	ENSG00000188641		"Dihydropyrimidine dehydrogenase deficiency, 274270 (3), Autosomal recessive; 5-fluorouracil toxicity, 274270 (3), Autosomal recessive"	Dpyd (MGI:2139667)			
chr1	98046069	98046170	1p22	1p21.3		614304	"MIR137, MIRN137"	Micro RNA 137	MIR137	406928							
chr1	98661283	98760499	1p21.3	1p21.3		614904	SNX7	Sorting nexin 7	SNX7	51375	ENSG00000162627			Snx7 (MGI:1923811)			
chr1	98890244	99006129	1p21.3	1p21.3		617287	"PLPPR5, LPPR5, PAP2D, PAP2"	Phospholipid phosphatase-related protein 5	PLPPR5	163404	ENSG00000117598			Plppr5 (MGI:1923019)			
chr1	99262955	99309583	1p21.3	1p21.3-p21.2		607813	"PLPPR4, LPPR4, PRG1, KIAA0455"	Phospholipid phosphatase-related protein 4	PLPPR4	9890	ENSG00000117600			Plppr4 (MGI:106530)			
chr1	99645874	99694540	1p21.2	1p21.2		610182	"PALMD, PALML"	Palmdelphin	PALMD	54873	ENSG00000099260			Palmd (MGI:2148896)			
chr1	99708698	99766629	1p21.2	1p21.2		611578	"FRRS1, SDR2"	Ferric chelate reductase 1	FRRS1	391059	ENSG00000156869			Frrs1 (MGI:108076)			
chr1	99850076	99924022	1p21	1p21.2		610860	"AGL, GDE"	"Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogen debranching enzyme)"	AGL	178	ENSG00000162688		"Glycogen storage disease IIIa, 232400 (3), Autosomal recessive; Glycogen storage disease IIIb, 232400 (3), Autosomal recessive"	Agl (MGI:1924809)			
chr1	99968400	100026978	1p21	1p21.2		605632	"SLC35A3, AMRS"	"Solute carrier family 35 (UDP-GlcNAc transporter), member 3"	SLC35A3	23443	ENSG00000117620	mutation identified in 1 family	"?Arthrogryposis, mental retardation, and seizures, 615553 (3), Autosomal recessive"	Slc35a3 (MGI:1917648)			
chr1	100082631	100133094	1p21.2	1p21.2		609321	"SASS6, SAS6, MCPH14"	SAS-6 centriolar assembly protein	SASS6	163786	ENSG00000156876	mutation identified in 1 MCPH14 family	"?Microcephaly 14, primary, autosomal recessive, 616402 (3), Autosomal recessive"	Sass6 (MGI:1920026)			
chr1	100186921	100249863	1p31	1p21.2		248610	"DBT, BCATE2"	Dihydrolipoamide branched chain transacylase (E2 component of branched chain keto acid dehydrogenase complex)	DBT	1629	ENSG00000137992	pseudogene on 3q24	"Maple syrup urine disease, type II, 248600 (3), Autosomal recessive"	Dbt (MGI:105386)			
chr1	100266157	100292768	1p21.2	1p21.2		611286	"RTCD1, RPC"	RNA terminal phosphate cyclase domain-containing protein 1	RTCA	8634	ENSG00000137996			Rtca (MGI:1913618)			
chr1	100345000	100520280	1p21	1p21.2		603504	"CDC14A, DFNB105"	"Cell division cycle 14, S. cerevisiae, homolog A"	CDC14A	8556	ENSG00000079335		"Deafness, autosomal recessive 105, 616958 (3), Autosomal recessive"	Cdc14a (MGI:2442676)			
chr1	100538171	100542026	1p21.2	1p21.2		607468	"GPR88, STRG, COCPMR"	G protein-coupled receptor 88	GPR88	54112	ENSG00000181656	mutation identified in 1 COCPMR family	"?Chorea, childhood-onset, with psychomotor retardation, 616939 (3), Autosomal recessive"	Gpr88 (MGI:1927653)			
chr1	100719639	100739044	1p32-p31	1p21.2		192225	VCAM1	Vascular cell adhesion molecule-1	VCAM1	7412	ENSG00000162692			Vcam1 (MGI:98926)			
chr1	100872371	100895410	1p12-p11	1p21.2		602411	EXTL2	Exostosin-like 2	EXTL2	2135	ENSG00000162694			Extl2 (MGI:1889574)			
chr1	100896075	100996912	1p21.2	1p21.2		611149	"SLC30A7, ZNT7"	"Solute carrier family 30 (zinc transporter), member 7"	SLC30A7	148867	ENSG00000162695			Slc30a7 (MGI:1913750)			
chr1	100975217	101025805	1p21.2	1p21.2		611075	"DPH5, HSPC143"	"DPH5, S. crevisiae, homolog of"	DPH5	51611	ENSG00000117543			Dph5 (MGI:1916990)			
chr1	101236748	101241519	1p21	1p21.2		601974	"S1PR1, EDG1, S1P1"	Sphingosine-1-phosphate receptor 1	S1PR1	1901	ENSG00000170989			S1pr1 (MGI:1096355)			
chr1	101800000	155100000	1p21.1-q21.3			612841	"HYPT5, MUHH2"	Hypotrichosis 5		100302560		max lod at D1S2881	"Hypotrichosis 5, 612841 (2), Autosomal dominant"				
chr1	101800000	111200000	1p21.1-p13.3			611107	MRT4	"Mental retardation, autosomal recessive, 4"	MRT4	100009675		between D2S429 and D1S187	"Mental retardation, autosomal recessive, 4, 611107 (2), Autosomal recessive"				
chr1	101800027	101997233	1p21	1p21.1		607567	"OLFM3, NOE3"	Olfactomedin 3	OLFM3	118427	ENSG00000118733			Olfm3 (MGI:2387329)			
chr1	102876466	103108579	1p21	1p21.1		120280	"COL11A1, STL2"	"Collagen XI, alpha-1 polypeptide"	COL11A1	1301	ENSG00000060718		"Fibrochondrogenesis 1, 228520 (3), Autosomal recessive; {Lumbar disc herniation, susceptibility to}, 603932 (3); Marshall syndrome, 154780 (3), Autosomal dominant; Stickler syndrome, type II, 604841 (3), Autosomal dominant"	Col11a1 (MGI:88446)			
chr1	103554643	103579533	1p21	1p21.1		104660	AMY2B	"Amylase, pancreatic, alpha-2B"	AMY2B	280	ENSG00000240038	distal to NGFB		"Amy2a2,Amy2a3,Amy2a4,Amy2a5 (MGI:3711220,MGI:3714985,MGI:3711258,MGI:88020)"			
chr1	103617331	103625779	1p21	1p21.1		104650	AMY2A	"Amylase, pancreatic, alpha-2A"	AMY2A	279	ENSG00000243480			Amy1 (MGI:88019)			
chr1	103655518	103664550	1p21	1p21.1		104700	AMY1A	"Amylase, salivary, alpha-1A"	AMY1A	276	ENSG00000237763	multiple amylase genes					
chr1	103687414	103696451	1p21	1p21.1		104701	AMY1B	"Amylase, salivary, alpha-1B"	AMY1B	277	ENSG00000174876						
chr1	103745429	103758691	1p21	1p21.1		104702	AMY1C	"Amylase, salivary, alpha-1C"	AMY1C	278	ENSG00000174876						
chr1	106700000	111200000	1p13.3			118943	CYMP	Chymosin pseudogene	CYMP	643160							
chr1	106700000	117200000	1p13			193000	VUR	Vesicoureteral reflux		54113			"Vesicoureteral reflux, 193000 (2), Autosomal dominant"				
chr1	107056644	107059293	1p13.3	1p13.3		608274	PRMT6	Protein arginine N-methyltransferase 6	PRMT6	55170	ENSG00000198890			Prmt6 (MGI:2139971)			
chr1	107139917	107484898	1p13.3	1p13.3		608818	"NTNG1, LMNT1, KIAA0976"	Netrin G1	NTNG1	22854	ENSG00000162631			Ntng1 (MGI:1934028)			
chr1	107571159	107964922	1p13.3	1p13.3		605541	VAV3	Vav3 oncogene	VAV3	10451	ENSG00000134215			Vav3 (MGI:1888518)			
chr1	108134721	108200357	1p36.13	1p13.3		608744	"SLC25A24, SCAMC1"	"Solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24"	SLC25A24	29957	ENSG00000085491		"Fontaine progeroid syndrome, 612289 (3), Autosomal dominant"	Slc25a24 (MGI:1917160)			
chr1	108222463	108244080	1p12	1p13.3		613994	NBPF4	"Neuroblastoma breakpoint family, member 4"	NBPF4	148545	ENSG00000196427						
chr1	108375970	108383613	1p12	1p13.3		613995	NBPF5	"Neuroblastoma breakpoint family, member 5"	NBPF5P	100507044							
chr1	108421495	108471902	1p12	1p13.3		613996	NBPF6	"Neuroblastoma breakpoint family, member 6"	NBPF6	653149	ENSG00000186086						
chr1	108648287	108661525	1p13.3	1p13.3		612178	"HENMT1, C1orf59, HEN1"	"Hen1 methyltransferase, arabidopsis, homolog of"	HENMT1	113802	ENSG00000162639			Henmt1 (MGI:1913965)			
chr1	108875349	108934334	1p13.1	1p13.3		609245	"GPSM2, LGN, PINS, DFNB82, CMCS"	G protein signaling modulator 2	GPSM2	29899	ENSG00000121957		"Chudley-McCullough syndrome, 604213 (3), Autosomal recessive"	Gpsm2 (MGI:1923373)			
chr1	108929507	108963498	1p13.3	1p13.3		617539	"CLCC1, MCLC"	Chloride channel CLIC-like 1	CLCC1	23155	ENSG00000121940			Clcc1 (MGI:2385186)			
chr1	108970210	109042227	1p13.3	1p13.3		615734	"WDR47, NEMITIN, KIAA0893"	WD repeat-containing protein 47	WDR47	22911	ENSG00000085433			Wdr47 (MGI:2139593)			
chr1	109064375	109076001	1p13.3	1p13.3		600774	"TAF13, TAF2K, MRT60"	"TAF13 RNA polymerase II, TATA box-binding protein-associated factor, 18kD"	TAF13	6884	ENSG00000197780		"Mental retardation, autosomal recessive 60, 617432 (3), Autosomal recessive"	Taf13 (MGI:1913500)			
chr1	109113962	109206780	1p13.3	1p13.3		611298	"KIAA1324, EIG121"	KIAA1324 gene	KIAA1324	57535				5330417C22Rik (MGI:1923930)			
chr1	109213892	109238181	1p13	1p13.3		607529	"SARS, SERS, NEDMAS"	Seryl-tRNA synthetase	SARS	6301	ENSG00000031698	mutation identified in 1 NEDMAS family	"?Neurodevelopmental disorder with microcephaly, ataxia, and seizures, 617709 (3), Autosomal recessive"	Sars (MGI:102809)			
chr1	109250018	109275755	1p21	1p13.3		604265	"CELSR2, EGFL2, MEGF3"	Cadherin EGF LAG seven-pass G-type receptor 3 (epidermal growth factor-like 2)	CELSR2	1952	ENSG00000143126			Celsr2 (MGI:1858235)			
chr1	109279553	109283171	1p13.1	1p13.3		613126	"PSRC1, DDA3"	Proline/serine-rich coiled-coil protein 1	PSRC1	84722	ENSG00000134222			Psrc1 (MGI:1913099)			
chr1	109309564	109397944	1p13.3	1p13.3		602458	"SORT1, NT3, LDLCQ6"	Sortilin	SORT1	6272	ENSG00000134243		"[Low density lipoprotein cholesterol level QTL6], 613589 (3), Autosomal dominant"	Sort1 (MGI:1338015)			
chr1	109399030	109426485	1p13	1p13.3		176844	"PSMA5, PSC5"	Proteasome component 5	PSMA5	5686	ENSG00000143106			Psma5 (MGI:1347009)			
chr1	109504174	109509750	1p13.3	1p13.3		615689	"AMIGO1, ALI2, KIAA1163"	Adhesion molecule with Ig-like domain 1	AMIGO1	57463	ENSG00000181754			Amigo1 (MGI:2653612)			
chr1	109539871	109545832	1p13.3	1p13.3		606916	GPR61	G protein-coupled receptor 61	GPR61	83873	ENSG00000156097			Gpr61 (MGI:2441719)			
chr1	109548563	109595842	1p13	1p13.3		139370	"GNAI3, ARCND1"	"Guanine nucleotide-binding protein (G-protein), alpha-inhibiting activity polypeptide-3"	GNAI3	2773	ENSG00000065135		"Auriculocondylar syndrome 1, 602483 (3), Autosomal dominant"	Gnai3 (MGI:95773)			
chr1	109598892	109598966	1p13.3	1p13.3		611189	MIR197	Micro rNA 197	MIR197	406974							
chr1	109603090	109619732	1p13	1p13.3		139340	"GNAT2, ACHM4"	"Guanine nucleotide-binding protein (G-protein), alpha-transducing (transducin) activity polypeptide-2"	GNAT2	2780	ENSG00000134183		"Achromatopsia 4, 613856 (3)"	Gnat2 (MGI:95779)			
chr1	109619812	109632054	1p13.3	1p13.3		102771	"AMPD2, SPG63, PCH9"	"Adenosine monophosphate deaminase-2, isoform L"	AMPD2	271	ENSG00000116337	mutation identified in 1 SPG63 family	"Pontocerebellar hypoplasia, type 9, 615809 (3), Autosomal recessive; ?Spastic paraplegia 63, 615686 (3), Autosomal recessive"	Ampd2 (MGI:88016)			
chr1	109656075	109665500	1p13.3	1p13.3		138333	GSTM4	Glutathione S-transferase M4	GSTM4	2948	ENSG00000168765			Gstm4 (MGI:95862)			
chr1	109668021	109683996	1p13.3	1p13.3		138380	"GSTM2, GST4"	"Glutathione S-transferase M2, muscle"	GSTM2	2946	ENSG00000213366			Gstm7 (MGI:1915562)			
chr1	109687795	109693744	1p13.3	1p13.3		138350	GSTM1	Glutathione S-transferase M1	GSTM1	2944	ENSG00000134184			Gstm2 (MGI:95861)			
chr1	109711750	109718267	1p13.3	1p13.3		138385	GSTM5	Glutathione S-transferase M5	GSTM5	2949	ENSG00000134201	pseudogene on chr.3		Gstm1 (MGI:95860)			
chr1	109733931	109741037	1p13.3	1p13.3		138390	"GSTM3, GST5"	"Glutathione S-transferase M3, brain"	GSTM3	2947	ENSG00000134202			Gstm5 (MGI:1309466)			
chr1	109750079	109764021	1p13.3	1p13.3		614989	"EPS8L3, EPS8R3"	EPS8-like protein 3	EPS8L3	79574	ENSG00000198758			Eps8l3 (MGI:2139743)			
chr1	109910505	109930993	1p21-p13	1p13.3		120420	"CSF1, MCSF"	Colony-stimulating factor-1 (macrophage)	CSF1	1435	ENSG00000184371	incorrectly assigned to chr.5		Csf1 (MGI:1339753)			
chr1	109984764	110023741	1p13.3	1p13.3		607826	"AHCYL1, DCAL, IRBIT"	Adenosylhomocysteine-like 1	AHCYL1	10768	ENSG00000168710			Ahcyl1 (MGI:2385184)			
chr1	110031576	110054640	1p13.3	1p13.3		617918	"STRIP1, FAR11A, FAM40A"	Striatin-interacting protein 1	STRIP1	85369	ENSG00000143093			Strip1 (MGI:2443884)			
chr1	110060374	110070699	1p21-p13	1p13.3		606014	"ALX3, FND1"	Aristaless-like homeobox 3	ALX3	257	ENSG00000156150		"Frontonasal dysplasia 1, 136760 (3), Autosomal recessive"	Alx3 (MGI:1277097)			
chr1	110112439	110113946	1p13.3	1p13.3		611127	UBL4B	Ubiquitin-like 4B	UBL4B	164153	ENSG00000186150			Ubl4b (MGI:1914841)			
chr1	110150513	110202201	1p13.3	1p13.3		610299	"SLC6A17, NTT4, MRT48"	"Solute carrier family 6 (neurotransmitter transporter), member 17"	SLC6A17	388662	ENSG00000197106		"Mental retardation, autosomal recessive 48, 616269 (3), Autosomal recessive"	Slc6a17 (MGI:2442535)			
chr1	110210713	110282648	1p13.3	1p13.3		176265	KCNC4	"Potassium voltage-gated channel, Shaw-related subfamily, member 4"	KCNC4	3749	ENSG00000116396			Kcnc4 (MGI:96670)			
chr1	110338928	110373004	1p13	1p13.3		606077	"RBM15, SPEN, OTT"	"One-twenty two protein (RNA binding motif protein 15; Spen, Drosophila, homolog of)"	RBM15	64783	ENSG00000162775		"Megakaryoblastic leukemia, acute, 606077 (2)"	Rbm15 (MGI:2443205)			
chr1	110401252	110407923	1p13.2	1p13.3		608521	"LAMTOR5, HBXIP, XIP"	"Late endosomal/lysosomal adaptor, mitogen-activated protein kinase and mammalian target of rapamycin activator 5"	LAMTOR5	10542	ENSG00000134248			Lamtor5 (MGI:1915826)			
chr1	110451165	110457353	1p21	1p13.3		606233	"PROK1, PK1, PRK1, EGVEGF"	Prokineticin 1	PROK1	84432	ENSG00000143125			Prok1 (MGI:2180370)			
chr1	110517216	110519174	1p13.1	1p13.3		602420	KCNA10	"Potassium voltage-gated channel, shaker-related subfamily, member 10"	KCNA10	3744	ENSG00000143105			Kcna10 (MGI:3037820)			
chr1	110593579	110631535	1p13.3	1p13.3		176262	"KCNA2, EIEE32"	"Potassium channel, voltage-gated, Shaker-related subfamily, member 2"	KCNA2	3737	ENSG00000177301		"Epileptic encephalopathy, early infantile, 32, 616366 (3), Autosomal dominant"	Kcna2 (MGI:96659)			
chr1	110653559	110675032	1p21-p13.3	1p13.3		176263	KCNA3	"Potassium voltage-gated channel, shaker-related subfamily, member 3"	KCNA3	3738	ENSG00000177272	mapped probably in error to chr.13		Kcna3 (MGI:96660)			
chr1	110871166	110899935	1p21-p13.3	1p13.3		151525	"CD53, MOX44"	CD53 antigen	CD53	963	ENSG00000143119			Cd53 (MGI:88341)			
chr1	110877251	110963961	1p12	1p13.3		615354	"LRIF1, RIF1"	Ligand-dependent nuclear receptor-interacting factor 1	LRIF1	55791	ENSG00000121931			Lrif1 (MGI:2445214)			
chr1	111117169	111140215	1p13.3	1p13.3		613360	"DRAM2, TMEM77, CORD21"	Damage-regulated autophagy modulator 2	DRAM2	128338	ENSG00000156171		"Cone-rod dystrophy 21, 616502 (3), Autosomal recessive"	Dram2 (MGI:1914421)			
chr1	111139382	111185103	1p13.3	1p13.3		616751	CEPT1	Choline/ethanolamine phosphotransferase 1	CEPT1	10390	ENSG00000134255			Cept1 (MGI:2139793)			
chr1	111185968	111204790	1p13.3	1p13.3-p13.2		615111	DENND2D	DENN/MADD domain-containing protein 2D	DENND2D	79961	ENSG00000162777			Dennd2d (MGI:2181193)			
chr1	111200000	115500000	1p13.2			617386	"NR1H5P, FXRB"	"Nuclear receptor subfamily 1, group H, member 5, pseudogene"	NR1H5P	643609							
chr1	111227079	111243439	1p13.3	1p13.2		601526	"CHI3L2, YKL39"	Chitinase 3-like 2	CHI3L2	1117	ENSG00000064886						
chr1	111290851	111320565	1p21.3-p13.1	1p13.2		606080	"CHIA, TSA1902, CHIT2"	"Chitinase, acidic"	CHIA	27159	ENSG00000134216			Chia1 (MGI:1932052)			
chr1	111324662	111353016	1p13.2	1p13.2		614234	"C1orf88, PIFO"	"Chromosome 1 open reading frame 88 (pitchfork, mouse, homolog of)"	PIFO	128344	ENSG00000173947			Pifo (MGI:1923670)			
chr1	111414314	111427776	1p13.2	1p13.2		603578	OVGP1	Oviductal glycoprotein 1	OVGP1	5016	ENSG00000085465			Ovgp1 (MGI:106661)			
chr1	111439889	111449307	1p13.2	1p13.2		611734	"WDR77, MEP50"	WD repeat-containing protein 77	WDR77	79084	ENSG00000116455			Wdr77 (MGI:1917715)			
chr1	111449120	111461917	1p13.2	1p13.2		603270	ATP5F1	"ATP synthase, H+ transporting, mitochondrial FO complex, subunit B, isoform 1"	ATP5PB	515	ENSG00000116459			Atp5f1 (MGI:1100495)			
chr1	111499428	111504120	1p21-p13	1p13.2		600445	ADORA3	Adenosine A3 receptor	ADORA3	140	ENSG00000282608			Adora3 (MGI:104847)			
chr1	111542222	111716694	1p13.3	1p13.2		179520	"RAP1A, KREV1"	RAS-related protein RAP1A	RAP1A	5906	ENSG00000116473	pseudogene on 14q24.3		Rap1a (MGI:97852)			
chr1	111755567	111767576	1p21.1-p13.2	1p13.2		606168	DDX20	DEAD/H box 20	DDX20	11218	ENSG00000064703			Ddx20 (MGI:1858415)			
chr1	111770661	111989576	1p13.3-p13.2	1p13.2		605411	"KCND3, KCND3S, KCND3L, SCA19, SCA22, BRGDA9"	"Potassium voltage-gated channel, Shal-related subfamily, member 3"	KCND3	3752	ENSG00000171385		"Brugada syndrome 9, 616399 (3), Autosomal dominant; Spinocerebellar ataxia 19, 607346 (3), Autosomal dominant"	Kcnd3 (MGI:1928743)			
chr1	112391084	112461163	1p13.2	1p13.2		615100	CTTNBP2NL	CTTNBP2 N terminus-like protein	CTTNBP2NL	55917	ENSG00000143079			Cttnbp2nl (MGI:1933137)			
chr1	112466540	112521287	1p13	1p13.2		601968	"WNT13, XWNT2"	"Wingless-type MMTV integration site family, member 13"	WNT2B	7482	ENSG00000134245			Wnt2b (MGI:1261834)			
chr1	112517443	112619880	1p13	1p13.2		617640	"ST7L, ST7R"	Suppressor of tumorigenicity 7-like protein	ST7L	54879	ENSG00000007341			St7l (MGI:2386964)			
chr1	112619452	112671618	1p13.2	1p13.2		601580	"CAPZA1, CAPPA1"	"Capping protein, muscle Z-line, alpha-1"	CAPZA1	829	ENSG00000116489			Capza1 (MGI:106227)			
chr1	112674311	112702376	1p13.2	1p13.2		610742	"MOV10, KIAA1631"	"Moloney leukemia virus 10, mouse, homolog of"	MOV10	4343	ENSG00000155363			Mov10 (MGI:97054)			
chr1	112701126	112707402	1p13.2	1p13.2		165380	"RHOC, ARHC, ARH9, RHOH9"	"RAS homolog gene family, member C (oncogene RHO H9)"	RHOC	389	ENSG00000155366	incorrectly assigned to chr.5		Rhoc (MGI:106028)			
chr1	112709993	112715327	1p13.2	1p13.2		609957	"PPM1J, PP2CZ, PPP2CZ"	"Protein phosphatase, magnesium-dependent, 1J"	PPM1J	333926	ENSG00000155367			Ppm1j (MGI:1919137)			
chr1	112718960	112727234	1p13.2	1p13.2		617497	"FAM19A3, TAFA3"	"Family with sequence similarity 19, member A3, CC motif chemokine-like"	FAM19A3	284467	ENSG00000184599			Fam19a3 (MGI:3046463)			
chr1	112911846	112956352	1p13.2-p12	1p13.2		600682	"SLC16A1, MCT1, HHF7, MCT1D"	"Solute carrier family 16 (monocarboxylic acid transporters), member 1"	SLC16A1	6566	ENSG00000155380		"Erythrocyte lactate transporter defect, 245340 (3), Autosomal dominant; Hyperinsulinemic hypoglycemia, familial, 7, 610021 (3), Autosomal dominant; Monocarboxylate transporter 1 deficiency, 616095 (3), Autosomal recessive, Autosomal dominant"	Slc16a1 (MGI:106013)			
chr1	113073169	113132259	1p13	1p13.2		608869	"LRIG2, LIG2, KIAA0806, UFS2"	Leucine-rich repeats- and immunoglobulin-like domains-containing protein 2	LRIG2	9860	ENSG00000198799		"Urofacial syndrome 2, 615112 (3), Autosomal recessive"	Lrig2 (MGI:2443718)			
chr1	113390473	113685922	1p21	1p13.2		615943	"MAGI3, KIAA1634"	"Membrane-associated guanylate kinase, WW and PDZ domains-containing, 3"	MAGI3	260425	ENSG00000081026			Magi3 (MGI:1923484)			
chr1	113697201	113759887	1p13	1p13.2		604950	PHTF1	Putative homeodomain transcription factor 1	PHTF1	10745	ENSG00000116793			Phtf1 (MGI:1332671)			
chr1	113761831	113812536	1p13.2	1p13.2		615858	"RSBN1, ROSBIN"	Round spermatid basic protein 1	RSBN1	54665	ENSG00000081019			Rsbn1 (MGI:2444993)			
chr1	113813810	113871760	1p13	1p13.2		600716	"PTPN22, PEP, PTPN8, LYP"	"Protein tyrosine phosphatase, nonreceptor-type 22"	PTPN22	26191	ENSG00000134242		"{Diabetes, type 1, susceptibility to}, 222100 (3), Autosomal recessive; {Rheumatoid arthritis, susceptibility to}, 180300 (3); {Systemic lupus erythematosus susceptibility to}, 152700 (3), Autosomal dominant"	Ptpn22 (MGI:107170)			
chr1	113894193	113905123	1p13.2	1p13.2		607245	"AP4B1, SPG47, CPSQ5"	"Adaptor-related protein complex 4, beta-1 subunit"	AP4B1	10717	ENSG00000134262		"Spastic paraplegia 47, autosomal recessive, 614066 (3), Autosomal recessive"	Ap4b1 (MGI:1337130)			
chr1	113904618	113914085	1p13.3-p13.1	1p13.2		609683	"DCLRE1B, SNM1B, APOLLO"	DNA cross-link repair protein 1B	DCLRE1B	64858	ENSG00000118655			Dclre1b (MGI:2156057)			
chr1	113979390	113982253	1p13.1	1p13.2		610088	"OLFML3, OLF44"	Olfactomedin-like 3	OLFML3	56944	ENSG00000116774			Olfml3 (MGI:1914877)			
chr1	114089291	114153918	1p13.2	1p13.2		607718	SYT6	Synaptotagmin 6	SYT6	148281	ENSG00000134207			Syt6 (MGI:1859544)			
chr1	114392776	114511191	1p13	1p13.2		605769	"TRIM33, TIF1G, RFG7, PTC7"	Tripartite motif-containing protein 33	TRIM33	51592	ENSG00000197323	fused with RET to form PTC7		Trim33 (MGI:2137357)			
chr1	114567556	114581643	1p21-p13.3	1p13.2		605783	"BCAS2, DAM1"	Breast carcinoma amplified sequence 2	BCAS2	10286	ENSG00000116752			Bcas2 (MGI:1915433)			
chr1	114673097	114695617	1p21-p13	1p13.2		102770	"AMPD1, MMDD"	"Adenosine monophosphate deaminase-1, muscle"	AMPD1	270	ENSG00000116748		"Myopathy due to myoadenylate deaminase deficiency, 615511 (3), Autosomal recessive"	Ampd1 (MGI:88015)			
chr1	114704463	114716893	1p13.2	1p13.2		164790	"NRAS, ALPS4, NS6, CMNS, NCMS"	Neuroblastoma RAS viral (v-ras) oncogene homolog	NRAS	4893	ENSG00000213281	cen-CD2-NGFB-NRAS	"Colorectal cancer, somatic, 114500 (3); Epidermal nevus, somatic, 162900 (3); Melanocytic nevus syndrome, congenital, somatic, 137550 (3); Neurocutaneous melanosis, somatic, 249400 (3); Noonan syndrome 6, 613224 (3), Autosomal dominant; ?RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic, 614470 (3); Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200 (3); Thyroid carcinoma, follicular, somatic, 188470 (3)"	Nras (MGI:97376)			
chr1	114716912	114758049	1p22	1p13.2		191510	"CSDE1, D1S155E, UNR"	"Cold-shock domain-containing E1, RNA-binding"	CSDE1	7812	ENSG00000009307	130bp 5' to NRAS		Csde1 (MGI:92356)			
chr1	114769478	114780686	1p13.2	1p13.2		611656	SIKE	Suppressor of IKK-epsilon	SIKE1	80143	ENSG00000052723			Sike1 (MGI:1913891)			
chr1	114854267	114995369	1p13	1p13.2		602162	"SYCP1, SCP1"	Synaptonemal complex protein-1	SYCP1	6847	ENSG00000198765			Sycp1 (MGI:105931)			
chr1	115029823	115035934	1p13	1p13.2		188540	"TSHB, CHNG4"	"Thyroid-stimulating hormone, beta polypeptide"	TSHB	7252	ENSG00000134200	centromeric to NGFB	"Hypothyroidism, congenital, nongoitrous 4, 275100 (3), Autosomal recessive"	Tshb (MGI:98848)			
chr1	115048010	115089500	1p13.2	1p13.2		613133	"TSPAN2, NET3"	Tetraspanin 2	TSPAN2	10100	ENSG00000134198			Tspan2 (MGI:1917997)			
chr1	115285914	115338252	1p13.1	1p13.2		162030	"NGF, NGFB, HSAN5"	"Nerve growth factor, beta"	NGF	4803	ENSG00000134259	same 310kb fragment as TSHB; order: cen-CD2-CD58-ATP1A1-NGF-TSHB-NRAS-tel	"Neuropathy, hereditary sensory and autonomic, type V, 608654 (3), Autosomal recessive"	Ngf (MGI:97321)			
chr1	115641952	115698223	1p13	1p13.1		610132	"VANGL1, STBM2"	Vang-like 1	VANGL1	81839	ENSG00000173218		"Caudal regression syndrome, 600145 (3), Autosomal dominant; {Neural tube defects, susceptibility to}, 182940 (3), Autosomal dominant"	Vangl1 (MGI:2159344)			
chr1	115700002	115768804	1p13.3-p11	1p13.1		114251	CASQ2	"Calsequestrin, fast-twitch, skeletal muscle-2"	CASQ2	845	ENSG00000118729		"Ventricular tachycardia, catecholaminergic polymorphic, 2, 611938 (3), Autosomal recessive"	Casq2 (MGI:1309469)			
chr1	115830776	115841125	1p12-p11	1p13.1		162361	"NHLH2, HEN2"	Nescient helix loop helix 2	NHLH2	4808	ENSG00000177551			Nhlh2 (MGI:97324)			
chr1	115976497	116070053	1p13.1	1p13.1		608275	"SLC22A15, FLIPT1"	"Solute carrier family 22 (organic cation transporter), member 15"	SLC22A15	55356	ENSG00000163393			Slc22a15 (MGI:3607704)			
chr1	116372985	116410258	1p13-p11	1p13.1		182310	ATP1A1	"ATPase, Na+K+ transporting, alpha-1 polypeptide"	ATP1A1	476	ENSG00000163399			Atp1a1 (MGI:88105)			
chr1	116500389	116571092	1p13	1p13.1		153420	"CD58, LFA3"	CD58 antigen (lymphocyte function-associated antigen 3)	CD58	965	ENSG00000116815	?same as MSK1; gene cloned					
chr1	116574397	116667754	1p13	1p13.1		603491	"IGSF3, LCDD"	"Immunoglobulin superfamily, member 3"	IGSF3	3321	ENSG00000143061	mutation identified in 1 LCDD family	"?Lacrimal duct defect, 149700 (3), Autosomal recessive"	Igsf3 (MGI:1926158)			
chr1	116754429	116769228	1p13.1	1p13.1		186990	CD2	"CD2 antigen (p50), sheep red blood cell receptor"	CD2	914	ENSG00000116824			Cd2 (MGI:88320)			
chr1	116909922	116990357	1p13.1-q21.3	1p13.1		601204	"PTGFRN, FPRP"	Prostaglandin F2 receptor negative regulator	PTGFRN	5738	ENSG00000134247			Ptgfrn (MGI:1277114)			
chr1	117060302	117107452	1p13.1	1p13.1		604718	TTF2	"Transcription termination factor, RNA polymerase II"	TTF2	8458	ENSG00000116830			Ttf2 (MGI:1921294)			
chr1	117107710	117121788	1p22	1p13.1		609318	TRIM45	Tripartite motif-containing protein 45	TRIM45	80263	ENSG00000134253			Trim45 (MGI:1918187)			
chr1	117143586	117210984	1p13.1	1p13-p12		608162	"VCTN1, B7H4, B7X, B7S1"	V-set domain containing T cell activation inhibitor 1	VTCN1	79679	ENSG00000134258			Vtcn1 (MGI:3039619)			
chr1	117367392	117528871	1p13	1p12		604345	MAN1A2	"Mannosidase, alpha, class 1A, member 2"	MAN1A2	10905	ENSG00000198162			Man1a2 (MGI:104676)			
chr1	117605981	117628388	1p12	1p12		613952	FAM46C	"Family with sequence similarity 46, member C"	FAM46C	54855	ENSG00000183508			Fam46c (MGI:1921895)			
chr1	117929748	117960425	1p13-p12	1p12		604737	WDR3	WD repeat-containing protein 3	WDR3	10885	ENSG00000065183			Wdr3 (MGI:2443143)			
chr1	117953594	118185268	1p12	1p12		616554	"SPAG17, PF6"	Sperm-associated antigen 17	SPAG17	200162	ENSG00000155761			Spag17 (MGI:1921612)			
chr1	118883042	118989555	1p13	1p12		604127	TBX15	T-box 15	TBX15	6913	ENSG00000092607		"Cousin syndrome, 260660 (3), Autosomal recessive"	Tbx15 (MGI:1277234)			
chr1	119031215	119140787	1p13.3-p13.1	1p12		604733	"WARS2, NEMMLAS"	Tryptophanyl-tRNA synthetase 2	WARS2	10352	ENSG00000116874		"Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, 617710 (3), Autosomal recessive"	Wars2 (MGI:1917810)			
chr1	119361912	119394129	1p13	1p12		605176	"HAO2, HAOX2"	Hydroxyacid oxidase 2	HAO2	51179	ENSG00000116882			Hao2 (MGI:96012)			
chr1	119414930	119423038	1p13.1	1p12		613890	HSD3B2	"Hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase, type 2 (adrenal, gonadal)"	HSD3B2	3284	ENSG00000203859		"Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, 201810 (3), Autosomal recessive"	Hsd3b1 (MGI:96233)			
chr1	119507202	119515057	1p13.1	1p12		109715	HSD3B1	"Hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase, type 1 (placental, peripheral)"	HSD3B1	3283	ENSG00000203857			"Hsd3b6,Hsd3b3,Hsd3b2 (MGI:109598,MGI:96235,MGI:96234)"			
chr1	119711795	119744225	1p12	1p12		606879	"PHGDH, NLS1, PHGDHD"	Phosphoglycerate dehydrogenase	PHGDH	26227	ENSG00000092621		"Neu-Laxova syndrome 1, 256520 (3), Autosomal recessive; Phosphoglycerate dehydrogenase deficiency, 601815 (3), Autosomal recessive"	Phgdh (MGI:1355330)			
chr1	119747995	119768931	1p13-p12	1p12		600234	HMGCS2	"3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2, mitochondrial"	HMGCS2	3158	ENSG00000134240		"HMG-CoA synthase-2 deficiency, 605911 (3), Autosomal recessive"	Hmgcs2 (MGI:101939)			
chr1	119794017	119811579	1p13.1-p12	1p12		609846	REG4	"Regenerating islet-derived family, member 4"	REG4	83998	ENSG00000134193			Reg4 (MGI:1914959)			
chr1	119833729	119844879	1p12	1p12		613997	NBPF7	"Neuroblastoma breakpoint family, member 7"	NBPF7	343505							
chr1	119893532	119896523	1p13-p11	1p12		604779	ADAM30	A disintegrin and metalloproteinase domain 30	ADAM30	11085	ENSG00000134249			Adam30 (MGI:1918328)			
chr1	119911552	120069702	1p13-p11	1p12		600275	"NOTCH2, AGS2, HJCYS"	"Notch, Drosophila, homolog  of, 2"	NOTCH2	4853	ENSG00000134250		"Alagille syndrome 2, 610205 (3), Autosomal dominant; Hajdu-Cheney syndrome, 102500 (3), Autosomal dominant"	Notch2 (MGI:97364)			
chr1	120155941	120176520	1q21.2-q21.3	1p12		604029	"SEC22L1, SEC22B"	"Secretion deficient 22, S. Cerevisiae, homolog-like 1"	SEC22B	9554	ENSG00000265808			Sec22b (MGI:1338759)			
chr1	120400000	123400000	1p11			606190	MNRI	"Meningioma, radiation-induced"		117192			"Meningioma, radiation-induced, 606190 (2)"				
chr1	120415026	120469669	1q21.1	1p11.2		613998	NBPF8	"Neuroblastoma breakpoint family, member 8"	NBPF8	728841							
chr1	120432203	120434108	1q21.1	1p11.2		608609	"C1orf152, COAS3"	Chromosome 1 open reading frame 152	PFN1P2	767846							
chr1	121087344	121097160	1p12	1p11.2		601502	FCGR1B	"Fc fragment of IgG, high affinity Ib, receptor for (CD64)"	FCGR1B	2210	ENSG00000198019						
chr1	121167645	121186895	1p11	1p11.2		614711	FAM72B	"Family with sequence similarity 72, member B"	FAM72B	653820	ENSG00000188610						
chr1	121184966	121392873	1p12	1p11.2		614704	SRGAP2C	SLIT-ROBO Rho GTPase-activating protein 2C	SRGAP2C	653464	ENSG00000171943						
chr1	123400000	248956422	1q			151628	LRE2	LINE retrotransposable element-2				inserted in DMD gene					
chr1	125100000	173000000	1q12-q24			605549	CORD8	Cone-rod dystrophy 8	CORD8	54109			"Cone-rod dystrophy 8, 605549 (2), Autosomal recessive"				
chr1	125100000	155100000	1q12-q21.3			612875	GNRHR2	Gonadotropin-releasing hormone receptor 2	GNRHR2	114814		?processed pseudogene					
chr1	125100000	156600000	1q12-q22			189890	TRNL	tRNA asparagine-like									
chr1	143200000	155100000	1q21			611152	AD13	Alzheimer disease-13		100188837		max lod D1S498	"{Alzheimer disease-13}, 611152 (2)"				
chr1	143200000	156600000	1q21-q22			608781	ASPG3	"Asperger syndrome, susceptibility to, 3"		449015		max lod at D1S484	"{Asperger syndrome susceptibility 3}, 608781 (2)"				
chr1	143200000	165500000	1q21-q23			605833	BMND2	Bone mineral density QTL 2		338027			"[Bone mineral density QTL 2], 605833 (2)"				
chr1	143200000	147500000	1q21.1			612474	"DEL1q21, C1DELq21"	Chromosome 1q21.1 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 1q21.1 deletion syndrome, 612474 (4), Autosomal dominant, Isolated cases"				
chr1	143200000	165500000	1q21-q23			608372	DFNA49	"Deafness, autosomal dominant 49"	DFNA49	317664		max lod at D1S3784 and D1S3786	"Deafness, autosomal dominant 49, 608372 (2), Autosomal dominant"				
chr1	143200000	165500000	1q21-q23			601412	DFNA7	"Deafness, autosomal dominant 7"	DFNA7	1689			"Deafness, autosomal dominant 7, 601412 (2), Autosomal dominant"				
chr1	143200000	147500000	1q21.1			612475	"DUP1q21, C1DUPq21"	Chromosome 1q21.1 duplication syndrome				contiguous gene duplication syndrome	"Chromosome 1q21.1 duplication syndrome, 612475 (4), Autosomal dominant, Isolated cases"				
chr1	143200000	165500000	1q21-q23			614013	"ERVK-7, HERV-KIII, HERV-K102"	"Endogenous retrovirus group K, member 7"	ERVK-7	449619							
chr1	143200000	147500000	1q21.1			613017	NBLST6	"Neuroblastoma, susceptibility to, 6"		100306939		?contiguous gene deletion or duplication disease	"{Neuroblastoma, susceptibility to, 6}, 613017 (2)"				
chr1	143200000	147500000	1q21.1			612970	"NBPF17P, NBPF23"	"Neuroblastoma breakpoint family, member 17, pseudogene"	NBPF17P	401967							
chr1	143200000	155100000	1q21			603935	PSORS4	Psoriasis susceptibility 4	PSORS4	10547			"{Psoriasis susceptibility 4}, 603935 (2)"				
chr1	143200000	155100000	1q21			605642	"PTCPRN, PRN1"	Papillary thyroid carcinoma with papillary renal neoplasia		79052			"Thyroid carcinoma, papillary, with papillary renal neoplasia, 605642 (2)"				
chr1	143200000	155100000	1q21			161900	"RFH1, AORF"	"Renal failure, progressive, with hypertension"		59331			"Nephropathy-hypertension, 161900 (2), Autosomal dominant"				
chr1	143200000	165500000	1q21-q23			613145	SLEB14	"Systemic lupus erythematosus, susceptibility to, 14"		100322878		associated with rs3093061	"{Systemic lupus erythematosus, susceptibility to, 14}, 613145 (2)"				
chr1	143200000	156600000	1q21-q22			182269	SPRR2C	Small proline-rich protein 2C	SPRR2C	6702		prob. pseudogene					
chr1	143200000	147500000	1q21.1			614747	UAQTL6	"Uric acid concentration, serum, quantitative trait locus 6"		100996935		associated with C/T variant at chr1_142697422	"[Uric acid concentration, serum, QTL6], 614747 (2)"				
chr1	143874742	143883732	1q21	1q21.1		601503	FCGR1C	"Fc fragment of IgG, high affinity Ic, receptor for (CD64)"	FCGR1CP	100132417							
chr1	143955363	143973518	1q21.2	1q21.1		616853	FAM72C	"Family with sequence similarity 72, member C"	FAM72C	554282	ENSG00000263513						
chr1	143972638	144069703	1q21.1	1q21.1		614705	SRGAP2D	SLIT-ROBO Rho GTPase-activating protein 2D	SRGAP2D	100996712							
chr1	144372874	144373658	1q21.1	1q21.1		608608	"PPIAL4A, COAS2"	Peptidylprolyl isomerase A (cyclophilin A)-like 4A	PPIAL4E	730262	ENSG00000271567						
chr1	144421385	144459463	1q21.1	1q21.1		610414	"NBPF15, MGC8902"	"Neuroblastoma breakpoint family, member 15"	NBPF15	284565	ENSG00000266338	contains 6 copies of DUF1220 domain					
chr1	144421385	144459463	1q21.1	1q21.1		614005	NBPF16	"Neuroblastoma breakpoint family, member 16"	NBPF15	284565	ENSG00000266338						
chr1	144887190	145095320	1q21.1	1q21.1		614703	SRGAP2B	SLIT-ROBO Rho GTPase-activating protein 2B	SRGAP2B	647135	ENSG00000196369						
chr1	145093804	145112691	1p21	1q21.1		614712	FAM72D	"Family with sequence similarity 72, member D"	FAM72D	728833	ENSG00000215784						
chr1	145287765	145287838	1p36.1	1q21.1		189880	"TRNAN1, TRN1, TRN"	tRNA asparagine	TRN-GTT2-1	7214							
chr1	145289899	145405777	1q21.1	1q21.1		614007	NBPF20	"Neuroblastoma breakpoint family, member 20"	NBPF20	100288142	ENSG00000162825						
chr1	145607959	145670976	1q21.1	1q21.1		612821	GPR89A	G protein-coupled receptor 89A	GPR89A	653519	ENSG00000117262			Gpr89 (MGI:1914799)			
chr1	145670851	145708200	1q21	1q21.1		603831	PDZK1	PDZ domain-containing 1	PDZK1	5174	ENSG00000174827			Pdzk1 (MGI:1928901)			
chr1	145719311	145739287	1q21.1	1q21.1		604463	"CD160, BY55"	CD160 antigen	CD160	11126	ENSG00000117281			Cd160 (MGI:1860383)			
chr1	145823182	145844401	1q21.1	1q21.1		617454	"POLR3C, RPC62, RPC3"	"Polymerase III, RNA, subunit C"	POLR3C	10623	ENSG00000186141			Polr3c (MGI:1921664)			
chr1	145848521	145859080	1q21	1q21.1		605987	PIAS3	Protein inhibitor of activated STAT3	PIAS3	10401	ENSG00000131788			Pias3 (MGI:1913126)			
chr1	145891207	145910188	1q21.1	1q21.1		604042	ITGA10	"Integrin, alpha-10"	ITGA10	8515	ENSG00000143127			Itga10 (MGI:2153482)			
chr1	145911347	145918923	1q21.1	1q21.1		603867	"PEX11B, PEX14B"	Peroxisome biogenesis 11B	PEX11B	8799	ENSG00000131779	mutation identified in 1 PEX14B patient	"?Peroxisome biogenesis disorder 14B, 614920 (3), Autosomal recessive"	Pex11b (MGI:1338882)			
chr1	145921555	145927535	1q12	1q21.1		605313	"RBM8A, RBM8B, TAR, C1DELq21.1, DEL1q21.1"	RNA-binding motif protein 8A	RBM8A	9939	ENSG00000265241	pseudogene on chr.14	"Thrombocytopenia-absent radius syndrome, 274000 (3), Autosomal recessive"	Rbm8a (MGI:1913129)			
chr1	145959036	145978847	1q21.1	1q21.1		617457	POLR3GL	"Polymerase III, RNA, subunit G-like"	POLR3GL	84265	ENSG00000121851			Polr3gl (MGI:1917120)			
chr1	145992425	145996630	1q21	1q21.1		606599	"TXNIP, VDUP1"	Thioredoxin-interacting protein	TXNIP	10628	ENSG00000265972			Txnip (MGI:1889549)			
chr1	146017467	146021821	1q21	1q21.1		608374	"HJV, HFE2A"	Hemojuvelin	HJV	148738	ENSG00000168509	between D1S442 and D1S2347	"Hemochromatosis, type 2A, 602390 (3), Autosomal recessive"	Hfe2 (MGI:1916835)			
chr1	146066317	146144803	1q21.1	1q21.1		614000	NBPF10	"Neuroblastoma breakpoint family, member 10"	NBPF10	100132406	ENSG00000271425						
chr1	146486331	146822033	1q21.1	1q21.1		610813	"HYDIN2, KIAA1864"	"Hydin, mouse, homolog of, 2"	HYDIN2	100288805		duplicated copy 16q22.2					
chr1	146938544	146996092	1q21.1	1q21.1		608607	"NBPF12, COAS1, KIAA1245"	"Neuroblastoma breakpoint family, member 12"	NBPF12	149013	ENSG00000268043						
chr1	147155105	147173365	1q21.1	1q21.1		602741	PRKAB2	"Protein kinase, AMP-activated, noncatalytic, beta-2"	PRKAB2	5565	ENSG00000131791			Prkab2 (MGI:1336185)			
chr1	147173193	147295765	1q21	1q21.1		613039	"CHD1L, ALC1"	Chromodomain helicase DNA-binding protein 1-like	CHD1L	9557	ENSG00000131778			Chd1l (MGI:1915308)			
chr1	147183962	147225797	1q21.1	1q21.1		603957	FMO5	Flavin-containing monooxygenase 5	FMO5	2330	ENSG00000131781			Fmo5 (MGI:1310004)			
chr1	147541500	147626218	1q21	1q21.2		602597	BCL9	B-cell CLL/lymphoma-9	BCL9	607	ENSG00000116128			Bcl9 (MGI:1924828)			
chr1	147626181	147670542	1q21	1q21.2		611471	"ACP6, LPAP, ACPL1"	"Acid phosphatase 6, lysophosphatide"	ACP6	51205	ENSG00000162836			Acp6 (MGI:1931010)			
chr1	147756198	147781126	1q21.2	1q21.2		121013	"GJA5, CX40, ATFB11"	"Gap junction protein, alpha-5, 40kD (connexin 40)"	GJA5	2702	ENSG00000265107		"Atrial fibrillation, familial, 11, 614049 (3), Autosomal dominant; Atrial standstill, digenic (GJA5/SCN5A), 108770 (3), Autosomal dominant"	Gja5 (MGI:95716)			
chr1	147902819	147915286	1q21.1	1q21.2		600897	"GJA8, CX50, CTRCT1, CZP1, CAE1"	Gap junction membrane channel protein alpha-8 (connexin 50)	GJA8	2703	ENSG00000121634		"Cataract 1, multiple types, 116200 (3), Autosomal dominant"	Gja8 (MGI:99953)			
chr1	147928373	147993591	1q21.1	1q21.2		612806	"GPR89B, GPHR"	G protein-coupled receptor 89B	GPR89B	51463	ENSG00000117262			Gpr89 (MGI:1914799)			
chr1	148102045	148152189	1q21.1	1q21.2		614001	NBPF11	"Neuroblastoma breakpoint family, member 11"	NBPF11	200030	ENSG00000263956						
chr1	148531384	148595716	1q21.1	1q21.2		614003	NBPF14	"Neuroblastoma breakpoint, member 14"	NBPF14	25832	ENSG00000270629						
chr1	148808180	149051276	1q21.1	1q21.2		608117	"PDE4DIP, MMGL, KIAA0454, KIAA0477"	Phosphodiesterase 4D-interacting protein	PDE4DIP	9659	ENSG00000178104			Pde4dip (MGI:1891434)			
chr1	149054032	149082310	1q21.1	1q21.2		613999	NBPF9	"Neuroblastoma breakpoint family, member 9"	NBPF9	400818	ENSG00000269713						
chr1	149475897	149556360	1q21.1	1q21.2		614006	NBPF19	"Neuroblastoma breakpoint family, member 19"	NBPF19	101060226	ENSG00000271383						
chr1	149782070	149792517	1q21.2-q21.3	1q21.2		146760	"FCGR1A, IGFR1, CD64"	"Fc fragment of IgG, high affinity Ia, receptor for (CD64)"	FCGR1A	2209	ENSG00000150337		"[IgG receptor I, phagocytic, familial deficiency of] (3)"	Fcgr1 (MGI:95498)			
chr1	149832656	149833051	1q21	1q21.2		142750	"H4FN, H4F2"	"H4 histone, family 2"	HIST2H4A	8370	ENSG00000270882	"100-200 histone genes; some on chromosome 6 and 12, as well as perhaps 7"		Hist1h4b (MGI:2448420)			
chr1	149840686	149841192	1q21	1q21.2		142780	"HIST2H3C, H3F2"	"Histone 2, H3c"	HIST2H3C	126961	ENSG00000203811			H3f3c (MGI:3650546)			
chr1	149842217	149842750	1q21	1q21.2		142720	"HIST2H2AA, H2AFO, H2A"	"Histone 2, H2aa"	HIST2H2AA3	8337	ENSG00000203812			"Hist2h2aa1,Hist2h2aa2 (MGI:96097,MGI:2448283)"			
chr1	149884459	149886681	1q21-q23	1q21.2		601831	"HIST2H2BE, H2B"	"Histone 2, H2be"	HIST2H2BE	8349	ENSG00000184678						
chr1	149886974	149887410	1q21-q23	1q21.2		602797	"HIST2H2AC, H2AFQ"	"Histone 2, H2ac"	HIST2H2AC	8338	ENSG00000184260			Hist2h2ac (MGI:2448316)			
chr1	149887468	149887915	1q21	1q21.2		615014	"HIST2H2AB, H2AB"	"Histone gene cluster 2, H2A histone family, member B"	HIST2H2AB	317772	ENSG00000184270			Hist2h2ab (MGI:2448314)			
chr1	149899581	149900794	1q21.2	1q21.2		613181	BOLA1	"BolA, E. coli, homolog of, 1"	BOLA1	51027	ENSG00000178096			Bola1 (MGI:1916418)			
chr1	149903317	149917881	1q21.2	1q21.2		185860	"SV2A, SV2"	Synaptic vesicle glycoprotein 2A	SV2A	9900	ENSG00000159164			Sv2a (MGI:1927139)			
chr1	149923316	149928251	1q21.2	1q21.2		605593	"SF3B4, SF3B49, SAP49, AFD1"	"Splicing factor 3B, subunit 4"	SF3B4	10262	ENSG00000143368		"Acrofacial dysostosis 1, Nager type, 154400 (3), Autosomal dominant"	Sf3b4 (MGI:109580)			
chr1	149940329	150010775	1q21.2	1q21.2		611748	"OTUD7B, CEZANNE"	OTU domain-containing protein 7B	OTUD7B	56957	ENSG00000264522			Otud7b (MGI:2654703)			
chr1	150067278	150145326	1q21-q22	1q21.2		610035	"VPS45A, VPS45, SCN5"	"Vacuolar protein sorting 45, yeast, homolog of, A"	VPS45	11311	ENSG00000136631		"Neutropenia, severe congenital, 5, autosomal recessive, 615285 (3), Autosomal recessive"	Vps45 (MGI:891965)			
chr1	150149433	150160064	1q21.2	1q21.2		608335	"PLEKHO1, CKIP1"	"Pleckstrin homology domain-containing protein, family O, member 1"	PLEKHO1	51177	ENSG00000023902			Plekho1 (MGI:1914470)			
chr1	150218416	150236155	1q22	1q21.2		609611	"ANP32E, LANPL"	"Acidic leucine-rich nuclear phosphoprotein 32 family, member E"	ANP32E	81611	ENSG00000143401						
chr1	150257257	150265861	1q21	1q21.2		604832	CA14	Carbonic anhydrase XIV	CA14	23632	ENSG00000118298			Car14 (MGI:1344341)			
chr1	150265398	150282178	1p36.13-q31.3	1q21.2		607629	APH1A	"Anterior pharynx defective 1, C. elegans, homolog of, A"	APH1A	51107	ENSG00000117362			Aph1a (MGI:2385110)			
chr1	150282532	150287092	1q21.2	1q21.2		615782	"CIART, CHRONO, GM129"	Circadian-associated repressor of transcription	CIART	148523	ENSG00000159208			Ciart (MGI:2684975)			
chr1	150293841	150308978	1q21	1q21.2		611984	MRPS21	Mitochondrial ribosomal protein S21	MRPS21	54460	ENSG00000266472	9 pseudogenes		Mrps21 (MGI:1913542)			
chr1	150321467	150353227	1q21.2	1q21.2		607301	"PRPF3, HPRP3, RP18"	"Precursor mRNA-processing factor 3, S. cerevisiae, homolog of"	PRPF3	9129	ENSG00000117360		"Retinitis pigmentosa 18, 601414 (3), Autosomal dominant"	Prpf3 (MGI:1918017)			
chr1	150364110	150476565	1q21.3	1q21.2		614695	RPRD2	Regulation of nuclear pre-mRNA domain-containing 2	RPRD2	23248	ENSG00000163125			Rprd2 (MGI:1922387)			
chr1	150487363	150507608	1q21.2	1q21.2		612805	"TARS2, COXPD21"	Threonyl-tRNA synthetase 2	TARS2	80222	ENSG00000143374	mutation identified in one COXPD21 family	"?Combined oxidative phosphorylation deficiency 21, 615918 (3), Autosomal recessive"	Tars2 (MGI:1919057)			
chr1	150508010	150513788	1q21	1q21.2		602201	"ECM1, URBWD"	Extracellular matrix protein-1	ECM1	1893	ENSG00000143369		"Urbach-Wiethe disease, 247100 (3), Autosomal recessive"	Ecm1 (MGI:103060)			
chr1	150515756	150518031	1q21.2	1q21.2		616092	"FALEC, FAL1"	Focally amplified long noncoding RNA in epithelial cancer	FALEC	100874054							
chr1	150549368	150560936	1q21	1q21.2		610113	"ADAMTSL4, TSRC1, ECTOL2"	ADAMTS-like 4	ADAMTSL4	54507	ENSG00000143382		"Ectopia lentis et pupillae, 225200 (3), Autosomal recessive; Ectopia lentis, isolated, autosomal recessive, 225100 (3), Autosomal recessive"	Adamtsl4 (MGI:2389008)			
chr1	150574550	150579737	1q21	1q21.2		159552	MCL1	Myeloid cell leukemia sequence 1 (BCL2-related)	MCL1	4170	ENSG00000143384			Mcl1 (MGI:101769)			
chr1	150600000	155100000	1q21.3			139450	HRM2	Hair morphology 2 (curly hair)		100379199		associated with rs11803731	"Hair, curly, 139450 (2), Autosomal dominant"				
chr1	150622122	150629621	1q21.2	1q21.3		603061	ENSA	"Endosulfine, alpha"	ENSA	2029	ENSG00000143420			Ensa (MGI:1891189)			
chr1	150646224	150697195	1q21.2	1q21.3		612208	"GOLPH3L, GPP34R"	Golgi phosphoprotein 3-like	GOLPH3L	55204	ENSG00000143457			Golph3l (MGI:1917129)			
chr1	150698058	150720909	1q21.3	1q21.3		609824	"HORMAD1, NOHMA"	HORMA domain-containing 1	HORMAD1	84072	ENSG00000143452			Hormad1 (MGI:1915231)			
chr1	150730195	150765956	1q21	1q21.3		116845	CTSS	Cathepsin S	CTSS	1520	ENSG00000163131			Ctss (MGI:107341)			
chr1	150796207	150808440	1q21	1q21.3		601105	CTSK	Cathepsin K	CTSK	1513	ENSG00000143387		"Pycnodysostosis, 265800 (3), Autosomal recessive"	Ctsk (MGI:107823)			
chr1	150809704	150876767	1q21	1q21.3		126110	ARNT	Aryl hydrocarbon receptor nuclear translocator	ARNT	405	ENSG00000143437			Arnt (MGI:88071)			
chr1	150926245	150964743	1q21	1q21.3		604396	SETDB1	"SET domain protein, bifurcated, 1"	SETDB1	9869	ENSG00000143379			Setdb1 (MGI:1934229)			
chr1	150965172	150975002	1q21.3	1q21.3		606920	"CERS2, LASS2"	Ceramide synthase 2	CERS2	29956	ENSG00000143418			Cers2 (MGI:1924143)			
chr1	150982022	150996062	1q21	1q21.3		603319	"ANXA9, ANX31"	Annexin A9 (annexin XXXI)	ANXA9	8416	ENSG00000143412			Anxa9 (MGI:1923711)			
chr1	151008390	151035712	1q21.3	1q21.3		617413	"PRUNE1, DRES17, NMIHBA"	Prune exopolyphosphatase 1	PRUNE1	58497	ENSG00000143363		"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies, 617481 (3), Autosomal recessive"	Prune1 (MGI:1925152)			
chr1	151036320	151047599	1q21.3	1q21.3		611275	"BNIPL, BNIPS, BNIPL1, BNIPL2"	BCL2/adenovirus E1B 19kD protein-interacting protein 2-like	BNIPL	149428	ENSG00000163141			Bnipl (MGI:2384749)			
chr1	151059674	151068496	1q21	1q21.3		604684	"MLLT11, AF1Q"	"Myeloid/lymphoid or mixed-lineage leukemia, translocated to, 11"	MLLT11	10962	ENSG00000213190			Mllt11 (MGI:1929671)			
chr1	151131684	151148407	1q21.3	1q21.3		609294	"SEMA6C, KIAA1869"	Semaphorin 6C	SEMA6C	10500	ENSG00000143434			Sema6c (MGI:1338032)			
chr1	151156628	151159748	1q21.2-q21.3	1q21.3		612112	"TNFAIP8L2, TIPE2"	Tumor necrosis factor-alpha-induced protein 8-like 2	TNFAIP8L2	79626	ENSG00000163154			Tnfaip8l2 (MGI:1917019)			
chr1	151166021	151170296	1q21.3	1q21.3		608095	"SCNM1, MGC3180"	Sodium channel modifier 1	SCNM1	79005	ENSG00000163156			Scnm1 (MGI:1341284)			
chr1	151169985	151176070	1q12	1q21.3		605834	TMOD4	"Tropomodulin 4, muscle"	TMOD4	29765	ENSG00000163157			Tmod4 (MGI:1355285)			
chr1	151176299	151190212	1q21	1q21.3		600607	"VPS72, CFL1, YL1"	"Vacuolar protein sorting 72, yeast, homolog of"	VPS72	6944	ENSG00000163159			Vps72 (MGI:1202305)			
chr1	151197953	151249535	1q22-q24	1q21.3		603275	PIP5K1A	"Phosphatidylinositol-4-phosphate 5-kinase, type I, alpha"	PIP5K1A	8394	ENSG00000143398			Pip5k1a (MGI:107929)			
chr1	151254699	151267478	1q21.3	1q21.3		601648	"PSMD4, S5A, RPN10"	"Proteasome 26S subunit, non-ATPase, 4"	PSMD4	5710	ENSG00000159352			Psmd4 (MGI:1201670)			
chr1	151281554	151291904	1q21.2	1q21.3		610568	"ZNF687, KIAA1441, PDB6"	Zinc finger protein 687	ZNF687	57592	ENSG00000143373	fused with AML1 in t(1;21)	"Paget disease of bone 6, 616833 (3), Autosomal dominant"	Zfp687 (MGI:1925516)			
chr1	151291796	151327714	1q21.1-q21.3	1q21.3		602758	PIK4CB	"Phosphatidylinositol 4-kinase, catalytic, beta polypeptide"	PI4KB	5298	ENSG00000143393			Pi4kb (MGI:1334433)			
chr1	151340639	151347318	1q21.1-q21.3	1q21.3		601863	RFX5	"Regulatory factor X, 5 (influences HLA class II expression)"	RFX5	5993	ENSG00000143390		"Bare lymphocyte syndrome, type II, complementation group C, 209920 (3), Autosomal recessive; Bare lymphocyte syndrome, type II, complementation group E, 209920 (3), Autosomal recessive"				
chr1	151364301	151372733	1q21-q22	1q21.3		604188	"SELENBP1, SP56"	Selenium-binding protein 1	SELENBP1	8991	ENSG00000143416			"Selenbp2,Selenbp1 (MGI:96825,MGI:104859)"			
chr1	151399564	151401935	1q21	1q21.3		602177	PSMB4	"Proteasome subunit, beta type, 4"	PSMB4	5692	ENSG00000159377			Psmb4 (MGI:1098257)			
chr1	151402723	151459464	1q21.3	1q21.3		614787	"POGZ, KIAA0461, MRD37, WHSUS"	POGO transposable element with ZNF domain	POGZ	23126	ENSG00000143442		"White-Sutton syndrome, 616364 (3), Autosomal dominant"	Pogz (MGI:2442117)			
chr1	151540293	151583582	1q21	1q21.3		600087	TUFT1	Tuftelin 1	TUFT1	7286	ENSG00000143367	?mutant in amelogenesis imperfecta		Tuft1 (MGI:109572)			
chr1	151612026	151699082	1q21.3	1q21.3		611541	"SNX27, MRT1"	Sorting nexin 27	SNX27	81609	ENSG00000143376			Snx27 (MGI:1923992)			
chr1	151696651	151716820	1q21	1q21.3		612678	"CELF3, TNRC4, BRUNOL1"	"CUGbp- and ELAV-like family, member 3"	CELF3	11189	ENSG00000159409			Celf3 (MGI:1926034)			
chr1	151759642	151763915	1q21	1q21.3		611824	MRPL9	Mitochondrial ribosomal protein L9	MRPL9	65005	ENSG00000143436			Mrpl9 (MGI:2137211)			
chr1	151762968	151771329	1q21.3	1q21.3		605138	"OAZ3, AZ3"	Ornithine decarboxylase antizyme 3	OAZ3	51686	ENSG00000143450			Oaz3 (MGI:1858170)			
chr1	151800263	151805441	1q21.3	1q21.3		609794	"LINGO4, LRRN6D"	Leucine-rich repeat- and Ig domain-containing NOGO receptor-interacting protein 4	LINGO4	339398	ENSG00000213171			Lingo4 (MGI:2444651)			
chr1	151806070	151832450	1q21	1q21.3		602943	"RORC, RORG, RZRG, IMD42"	RAR-related orphan receptor C	RORC	6097	ENSG00000143365		"Immunodeficiency 42, 616622 (3), Autosomal recessive"	Rorc (MGI:104856)			
chr1	151847100	151853696	1q21.3	1q21.3		615653	"THEM5, ACOT15"	Thioesterase superfamily member 5	THEM5	284486				Them5 (MGI:1913448)			
chr1	151870865	151909884	1q21	1q21.3		606388	CTMP	C-terminal modulator protein	THEM4	117145	ENSG00000159445			Them4 (MGI:1923028)			
chr1	151982909	151994237	1q21	1q21.3		114085	"S100A10, CAL1L"	"S100 calcium-binding protein A10 (annexin II ligand, calpactin I, light polypeptide (p11))"	S100A10	6281	ENSG00000197747	on chr.3 in mouse		S100a10 (MGI:1339468)			
chr1	152032505	152037034	1q21	1q21.3		603114	S100A11	S100 calcium-binding protein A11	S100A11	6282	ENSG00000163191			S100a11-ps (MGI:3645720)			
chr1	152106316	152115453	1q21.3	1q21.3		190370	"TCHH, THH, THL, TRHY, UHS3"	Trichohyalin	TCHH	7062	ENSG00000159450	mutation identified in 1 UHS3 patient	"?Uncombable hair syndrome 3, 617252 (3), Autosomal recessive"				
chr1	152153594	152159227	1q21	1q21.3		613259	RPTN	Repetin	RPTN	126638	ENSG00000215853			Rptn (MGI:1099055)			
chr1	152212075	152224195	1q21.3	1q21.3		616293	HRNR	Hornerin	HRNR	388697	ENSG00000197915						
chr1	152302174	152325202	1q21	1q21.3		135940	"FLG, ATOD2"	Filaggrin	FLG	2312	ENSG00000143631		"{Dermatitis, atopic, susceptibility to, 2}, 605803 (3); Ichthyosis vulgaris, 146700 (3), Autosomal dominant"				
chr1	152348734	152360027	1q21.3	1q21.3		616284	"FLG2, IFPS"	"Filaggrin family, member 2"	FLG2	388698	ENSG00000143520						
chr1	152510843	152512176	1q21	1q21.3		612619	"LCE5A, LEP18"	Late cornified envelope protein 5A	LCE5A	254910	ENSG00000186207						
chr1	152514501	152516009	1q21.3	1q21.3		617426	"CRCT1, NICE1, C1orf42"	Cysteine-rich c-terminal 1	CRCT1	54544	ENSG00000169509						
chr1	152565653	152566769	1q21	1q21.3		612617	"LCE3E, LEP17"	Late cornified envelope protein 3E	LCE3E	353145	ENSG00000185966						
chr1	152579383	152580503	1q21	1q21.3		612616	"LCE3D, LEP16"	Late cornified envelope protein 3D	LCE3D	84648	ENSG00000163202	within intron 2 of LCE3C					
chr1	152600661	152601085	1q21	1q21.3		612615	"LCE3C, LEP15"	Late cornified envelope protein 3C	LCE3C	353144	ENSG00000244057						
chr1	152613810	152614097	1q21	1q21.3		612614	"LCE3B, LEP14"	Late cornified envelope protein 3B	LCE3B	353143	ENSG00000187238						
chr1	152622833	152623102	1q21	1q21.3		612613	"LCE3A, LEP13"	Late cornified envelope protein 3A	LCE3A	353142	ENSG00000185962						
chr1	152663410	152664658	1q21	1q21.3		612612	"LCE2D, LEP12"	Late cornified envelope protein 2D	LCE2D	353141	ENSG00000187223						
chr1	152675314	152676573	1q21	1q21.3		612611	"LCE2C, LEP11"	Late cornified envelope protein 2C	LCE2C	353140	ENSG00000187180						
chr1	152686122	152687400	1q21	1q21.3		612610	"LCE2B, LEP10, XP5"	Late cornified envelope protein 2B	LCE2B	26239	ENSG00000159455						
chr1	152698363	152699441	1q21	1q21.3		612609	"LCE2A, LEP9"	Late cornified envelope protein 2A	LCE2A	353139	ENSG00000187173						
chr1	152709046	152709433	1q21	1q21.3		612618	"LCE4A, LEP8"	Late cornified envelope protein 4A	LCE4A	199834	ENSG00000187170						
chr1	152758029	152762052	1q21	1q21.3		613260	KPRP	Keratinocyte proline-rich protein	KPRP	448834	ENSG00000203786			Kprp (MGI:1920981)			
chr1	152776371	152776968	1q21	1q21.3		612608	"LCE1F, LEP6"	Late cornified envelope protein 1F	LCE1F	353137	ENSG00000240386						
chr1	152786276	152788425	1q21	1q21.3		612607	LCE1E	Late cornified envelope protein 1E	LCE1E	353135	ENSG00000186226						
chr1	152796750	152798180	1q21	1q21.3		612606	"LCE1D, LEP4"	Late cornified envelope protein 1D	LCE1D	353134	ENSG00000172155						
chr1	152804834	152806630	1q21	1q21.3		612605	"LCE1C, LEP3"	Late cornified envelope 1C	LCE1C	353133	ENSG00000197084						
chr1	152811970	152813108	1q21	1q21.3		612604	"LCE1B, LEP2"	Late cornified envelope protein 1B	LCE1B	353132	ENSG00000196734						
chr1	152827472	152828096	1q21	1q21.3		612603	"LCE1A, LEP1"	Late cornified envelope protein 1A	LCE1A	353131	ENSG00000186844						
chr1	152878321	152885046	1q21	1q21.3		601148	"SMCP, MCSP, MCS"	Sperm mitochondria-associated cysteine-rich protein	SMCP	4184	ENSG00000163206						
chr1	152908544	152911885	1q21	1q21.3		147360	IVL	Involucrin	IVL	3713	ENSG00000163207						
chr1	152968754	152972601	1q21	1q21.3		616363	SPRR4	Small proline-rich protein 4	SPRR4	163778	ENSG00000184148						
chr1	152984087	152985813	1q21-q22	1q21.3		182265	SPRR1A	Small proline-rich protein 1A	SPRR1A	6698	ENSG00000169474			Sprr1a (MGI:106660)			
chr1	153001746	153003855	1q21-q22	1q21.3		182271	SPRR3	Small proline-rich protein 3	SPRR3	6707	ENSG00000163209			Sprr3 (MGI:1330237)			
chr1	153031202	153032899	1q21-q22	1q21.3		182266	SPRR1B	Small proline-rich protein 1B	SPRR1B	6699	ENSG00000169469						
chr1	153039724	153041143	1q21.3	1q21.3		617587	SPRR2D	Small proline-rich protein 2D	SPRR2D	6703	ENSG00000163216						
chr1	153056119	153057511	1q21-q22	1q21.3		182267	SPRR2A	Small proline-rich protein 2A	SPRR2A	6700	ENSG00000241794	about 7 SPRR2 genes					
chr1	153070225	153071607	1q21-q22	1q21.3		182268	SPRR2B	Small proline-rich protein 2B	SPRR2B	6701	ENSG00000196805						
chr1	153093134	153094527	1q21.3	1q21.3		617588	SPRR2E	Small proline-rich protein 2E	SPRR2E	6704	ENSG00000203785						
chr1	153112120	153119459	1q21.3	1q21.3		617589	SPRR2F	Small proline-rich protein 2F	SPRR2F	6705	ENSG00000244094						
chr1	153149581	153195376	1q21.3	1q21.3		617590	SPRR2G	Small proline-rich protein 2G	SPRR2G	6706	ENSG00000159516						
chr1	153203429	153205124	1q21	1q21.3		611042	LELP1	Late cornified envelope-like proline-rich 1	LELP1	149018	ENSG00000203784						
chr1	153259634	153262124	1q21	1q21.3		152445	LOR	Loricrin	LOR	4014	ENSG00000203782		"Vohwinkel syndrome with ichthyosis, 604117 (3), Autosomal dominant"				
chr1	153297588	153312974	1q21	1q21.3		608197	PGRPIA	"Peptidoglycan recognition protein, intermediate, alpha"	PGLYRP3	114771	ENSG00000159527			Pglyrp3 (MGI:2685266)			
chr1	153327409	153348843	1q21	1q21.3		608198	PGRPIB	"Peptidoglycan recognition protein, intermediate, beta"	PGLYRP4	57115	ENSG00000163218			Pglyrp4 (MGI:2686324)			
chr1	153357853	153361026	1q12-q22	1q21.3		123886	"S100A9, CAGB, CFAG"	S100 calcium-binding protein A9 (calgranulin B)	S100A9	6280	ENSG00000163220			S100a9 (MGI:1338947)			
chr1	153373707	153375598	1q21	1q21.3		603112	"S100A12, CAAF1, CGRP"	S100 calcium-binding protein A12	S100A12	6283	ENSG00000163221	between S100A8 and S100A9					
chr1	153390031	153422582	1q21	1q21.3		123885	"S100A8, CAGA, CFAG"	S100 calcium-binding protein A8 (calgranulin A)	S100A8	6279	ENSG00000143546	over-expressed in 1q21-linked psoriasis		S100a8 (MGI:88244)			
chr1	153416523	153423224	1q21.3	1q21.3		617427	"S100A7A, S100A15, NICE2"	S100 calcium-binding protein A7A	S100A7A	338324	ENSG00000184330						
chr1	153457743	153460660	1q21	1q21.3		600353	S100A7	S100 calcium-binding protein A7	S100A7	6278	ENSG00000143556						
chr1	153534598	153536240	1q21	1q21.3		114110	"S100A6, CACY"	S100 calcium-binding protein A6 (calcyclin)	S100A6	6277	ENSG00000197956			S100a6 (MGI:1339467)			
chr1	153537113	153543513	1q21	1q21.3		176991	"S100A5, S100D"	S100 calcium-binding protein A5	S100A5	6276	ENSG00000196420			S100a5 (MGI:1338915)			
chr1	153543618	153545805	1q21	1q21.3		114210	"S100A4, CAPL"	"S100 calcium-binding protein A4 (calcium protein, calvasculin, metastasin, murine placental homolog)"	S100A4	6275	ENSG00000196154			S100a4 (MGI:1330282)			
chr1	153547332	153549257	1q21	1q21.3		176992	"S100A3, S100E"	S100 calcium-binding protein A3	S100A3	6274	ENSG00000188015			S100a3 (MGI:1338849)			
chr1	153561107	153565829	1q21	1q21.3		176993	"S100A2, S100L"	S100 calcium-binding protein A2	S100A2	6273	ENSG00000196754						
chr1	153606882	153613167	1p21.3	1q21.3		617437	"S100A16, AAG13"	S100 calcium-binding protein A16	S100A16	140576	ENSG00000188643			S100a16 (MGI:1915110)			
chr1	153614254	153616916	1q21	1q21.3		607986	"S100A14, BCMP84"	S100 Calcium-binding protein A14	S100A14	57402	ENSG00000189334			S100a14 (MGI:1913416)			
chr1	153618798	153634091	1q21	1q21.3		601989	S100A13	S100 calcium-binding protein A13	S100A13	6284	ENSG00000189171			S100a13 (MGI:109581)			
chr1	153628396	153632036	1q21	1q21.3		176940	S100A1	"S100 protein, alpha polypeptide"	S100A1	6271	ENSG00000160678			S100a1 (MGI:1338917)			
chr1	153633981	153646305	1q21.3	1q21.3		614206	"CHTOP, C10orf77, SRAG, FOP"	Chromatin target of PRMT1	CHTOP	26097	ENSG00000160679						
chr1	153658653	153661851	1q22	1q21.3		607007	"SNAPIN, SNAPAP, BLOC1S7, BLOS7"	SNAP-associated protein	SNAPIN	23557	ENSG00000143553			Snapin (MGI:1333745)			
chr1	153678648	153693991	1q21-q22	1q21.3		108960	"NPR1, ANPRA"	Natriuretic peptide receptor A/guanylate cyclase A	NPR1	4881	ENSG00000169418			Npr1 (MGI:97371)			
chr1	153728066	153774807	1q21.3	1q21.3		611347	"INTS3, INT3, SOSSA"	Integrator complex subunit 3	INTS3	65123	ENSG00000143624			Ints3 (MGI:2140050)			
chr1	153774353	153780159	1q21.3	1q21.3		604193	"SLC27A3, FATP3"	"Solute carrier family 27 (fatty acid transporter), member 3"	SLC27A3	11000	ENSG00000143554			Slc27a3 (MGI:1347358)			
chr1	153804906	153923952	1q23.1	1q21.3		614998	"GATAD2B, KIAA1150, p68, MRD18"	GATA zinc finger domain-containing protein 2B	GATAD2B	57459	ENSG00000143614		"Mental retardation, autosomal dominant 18, 615074 (3), Autosomal dominant"	Gatad2b (MGI:2443225)			
chr1	153947671	153958655	1q21.3	1q21.3		608972	"CRTC2, TORC2"	CREB-regulated transcription coactivator 2	CRTC2	200186	ENSG00000160741			Crtc2 (MGI:1921593)			
chr1	153959098	153968183	1q21	1q21.3		604740	"SLC39A1, ZIRTL"	"Solute carrier family 39 (zinc transporter), member 3 (zinc/iron-regulated transporter-like)"	SLC39A1	27173	ENSG00000143570	REc		Slc39a1 (MGI:1353474)			
chr1	153967486	153974363	1q21.3	1q21.3		607138	"CREB3L4, CREB4, AIBZIP"	cAMP responsive element binding protein 3-like 4	CREB3L4	148327	ENSG00000143578			Creb3l4 (MGI:1916603)			
chr1	153974268	153977974	1q21	1q21.3		604671	"JTB, PAR"	Jumping translocation breakpoint	JTB	10899	ENSG00000143543			Jtb (MGI:1346082)			
chr1	153981616	153990643	1q21.3	1q21.3		602672	RAB13	"RAB13, member RAS oncogene family"	RAB13	5872	ENSG00000143545	previously assigned to 12q13 by in situ hybridization		Rab13 (MGI:1927232)			
chr1	153990754	153992154	1q21	1q21.3		603702	"RPS27, MPS1, DBA17"	Ribosomal protein S27	RPS27	6232	ENSG00000185088	mutation identified in 1 DBA17 patient	"?Diamond-Blackfan anemia 17, 617409 (3), Autosomal dominant"				
chr1	154155303	154192134	1q22-q23	1q21.3		191030	"TPM3, NEM1, CFTD, CAPM1"	Tropomyosin 3	TPM3	7170	ENSG00000143549	TRK = chimera of TPM3 and NTRK1; NEM1 to 1q21-q23 by Fd	"CAP myopathy 1, 609284 (3), Autosomal recessive, Autosomal dominant; Myopathy, congenital, with fiber-type disproportion, 255310 (3), Autosomal recessive, Autosomal dominant; Nemaline myopathy 1, autosomal dominant or recessive, 609284 (3), Autosomal recessive, Autosomal dominant"	Tpm3 (MGI:1890149)			
chr1	154206700	154220796	1q21.3	1q21.3		617428	"C1orf43, NS5ATP4, NICE3"	Chromosome 1 open reading frame 43	C1orf43	25912	ENSG00000143612			4933434E20Rik (MGI:1914027)			
chr1	154220171	154271509	1q21.3	1q21.3		616472	"UBAP2L, NICE4"	Ubiquitin-associated protein 2-like	UBAP2L	9898	ENSG00000143569						
chr1	154272562	154275874	1q21.3	1q21.3		605998	"HAX1, SCN3"	HCLS1-associated protein X1	HAX1	10456	ENSG00000143575		"Neutropenia, severe congenital 3, autosomal recessive, 610738 (3), Autosomal recessive"	Hax1 (MGI:1346319)			
chr1	154321058	154325324	1q21.3	1q21.3		606578	AQP10	Aquaporin 10	AQP10	89872	ENSG00000143595						
chr1	154325559	154351303	1q21.3	1q21.3		605867	"ATP8B2, ATPID"	"ATPase, class I, type 8B, member 2"	ATP8B2	57198	ENSG00000143515			Atp8b2 (MGI:1859660)			
chr1	154405192	154469449	1q21.3	1q21.3		147880	"IL6R, IL6RQ, IL6Q"	Interleukin-6 receptor	IL6R	3570	ENSG00000160712	IL6R-like gene on chr.9	"[Interleukin 6, serum level of, QTL], 614752 (3); [Interleukin-6 receptor, soluble, serum level of, QTL], 614689 (3)"	Il6ra (MGI:105304)			
chr1	154467194	154502559	1q21.3	1q21.3		610482	SHE	SH2 domain-containing protein E	SHE	126669	ENSG00000169291			She (MGI:1099462)			
chr1	154548574	154558643	1q21.3	1q21.3		617429	"UBE2Q1, GTAP, NICE5"	Ubiquitin-conjugating enzyme E2Q family member 1	UBE2Q1	55585	ENSG00000160714			Ube2q1 (MGI:1917343)			
chr1	154567780	154584707	1q21	1q21.3		118507	"CHRNB2, EFNL3"	"Cholinergic receptor, nicotinic, beta polypeptide-2"	CHRNB2	1141	ENSG00000160716	linked to AMY in mouse	"Epilepsy, nocturnal frontal lobe, 3, 605375 (3)"	Chrnb2 (MGI:87891)			
chr1	154582056	154631559	1q21.3	1q21.3		146920	"ADAR, DRADA, DSH, DSRAD, IFI4, G1P1, AGS6"	"Adenosine deaminase, RNA-specific"	ADAR	103	ENSG00000160710		"Aicardi-Goutieres syndrome 6, 615010 (3), Autosomal recessive; Dyschromatosis symmetrica hereditaria, 127400 (3), Autosomal dominant"	Adar (MGI:1889575)			
chr1	154697461	154870277	1q21.3	1q21.3		602983	"KCNN3, SK3, SKCA3"	"Potassium channel, calcium-activated, intermediate/small conductance, subfamily N, member 3"	KCNN3	3782	ENSG00000143603			Kcnn3 (MGI:2153183)			
chr1	154924731	154942688	1q21.3	1q21.3		607622	"PMVK, PMK, POROK1"	Phosphomevalonate kinase	PMVK	10654	ENSG00000163344		"Porokeratosis 1, multiple types, 175800 (3), Autosomal dominant"	Pmvk (MGI:1915853)			
chr1	154957025	154961781	1q21.3	1q21.3		606903	PYGO2	"Pygopus, Drosophila, homolog of, 2"	PYGO2	90780	ENSG00000163348			Pygo2 (MGI:1916161)			
chr1	154962297	154974491	1q21	1q21.3		600560	SHC1	SHC (Src homology 2 domain-containing) transforming protein-1	SHC1	6464	ENSG00000160691			Shc1 (MGI:98296)			
chr1	154974641	154979248	1q21.3	1q21.3		116900	"CKS1B, CKS1"	CDC28 protein kinase 1B	CKS1B	1163	ENSG00000173207	previously to 8q21 by FISH		Cks1b (MGI:1889208)			
chr1	154983293	154993110	1q21.3	1q21.3		610595	"FLAD1, FADS, LSMFLAD"	"Flavin adenine dinucleotide synthetase, S. cerevisiae, homolog of"	FLAD1	80308	ENSG00000160688		"Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency, 255100 (3), Autosomal recessive"	Flad1 (MGI:2443030)			
chr1	154993585	154994314	1q22	1q21.3		607377	"LENEP, LEP503"	Lens epithelial protein	LENEP	55891	ENSG00000163352			Lenep (MGI:1930020)			
chr1	155002627	155018524	1q21.3	1q21.3		607646	"ZBTB7B, ZFP67, CKROX, THPOK"	Zinc finger- and BTB domain-containing protein 7B	ZBTB7B	51043	ENSG00000160685			Zbtb7b (MGI:102755)			
chr1	155051271	155062775	1q21.3	1q21.3		605548	"ADAM15, MDC15"	A disintegrin and metalloproteinase domain 15	ADAM15	8751	ENSG00000143537			Adam15 (MGI:1333882)			
chr1	155063736	155069552	1q21-q22	1q21.3		601380	"EFNA4, EPLG4"	eph-related receptor tyrosine kinase ligand 4 (ephrin-A4)	EFNA4	1945	ENSG00000243364			Efna4 (MGI:106643)			
chr1	155078871	155087537	1q21-q22	1q21.3		601381	"EFNA3, EPLG3"	eph-related receptor tyrosine kinase ligand 3 (ephrin A3)	EFNA3	1944	ENSG00000143590			Efna3 (MGI:106644)			
chr1	155127872	155134909	1q21-q22	1q22		191164	"EFNA1, EPLG1, TNFAIP4"	"eph-related receptor tyrosine kinase ligand 1 (tumor necrosis factor, alpha-induced protein 4)"	EFNA1	1942	ENSG00000169242			Efna1 (MGI:103236)			
chr1	155135343	155138857	1q22	1q22		613683	"SLC50A1, RAG1AP1"	"Solute carrier family 50 (sugar transporter), member 1"	SLC50A1	55974	ENSG00000169241			Slc50a1 (MGI:107417)			
chr1	155139890	155140572	1q12-q21	1q22		605951	"DPM3, CDG1O"	Dolichyl-phosphate mannosyltransferase 3	DPM3	54344	ENSG00000179085		"Congenital disorder of glycosylation, type Io, 612937 (3)"	Dpm3 (MGI:1915813)			
chr1	155173380	155184970	1q21	1q22		600986	GENEY	Gene Y	TRIM46	80128	ENSG00000163462			Trim46 (MGI:2673000)			
chr1	155185823	155192914	1q21	1q22		158340	"MUC1, PUM, MCKD1"	"Mucin 1, transmembrane"	MUC1	4582	ENSG00000185499	5cM proximal to SPTA1	"Medullary cystic kidney disease 1, 174000 (3), Autosomal dominant"				
chr1	155195587	155209179	1q21	1q22		188062	"THBS3, TSP3"	Thrombospondin 3	THBS3	7059	ENSG00000169231			Thbs3 (MGI:98739)			
chr1	155208698	155213838	1q21	1q22		600605	"MTX1, MTXN"	Metaxin 1	MTX1	4580	ENSG00000173171	between GBA and TSP3		Mtx1 (MGI:103025)			
chr1	155234447	155244861	1q21	1q22		606463	GBA	"Glucosidase, acid beta"	GBA	2629	ENSG00000177628	pseudogene GBAP ~16kb 3' to GBA	"Gaucher disease, perinatal lethal, 608013 (3), Autosomal recessive; Gaucher disease, type I, 230800 (3), Autosomal recessive; Gaucher disease, type II, 230900 (3), Autosomal recessive; Gaucher disease, type III, 231000 (3), Autosomal recessive; Gaucher disease, type IIIC, 231005 (3), Autosomal recessive; {Lewy body dementia, susceptibility to}, 127750 (3), Autosomal dominant; {Parkinson disease, late-onset, susceptibility to}, 168600 (3), Isolated cases, Multifactorial"	Gba (MGI:95665)			
chr1	155255978	155262384	1q21	1q22		606913	"SCAMP3, PROPIN1"	Secretory carrier membrane protein 3	SCAMP3	10067	ENSG00000116521			Scamp3 (MGI:1346346)			
chr1	155262867	155273528	1p31	1q22		602989	CLK2	CDC-like kinase 2	CLK2	1196	ENSG00000176444	near GDLD and PRKAA2; conflicting assignment 1q21		Clk2 (MGI:1098669)			
chr1	155277426	155289847	1q22	1q22		609973	"HCN3, KIAA1535"	Hyperpolarization-activated cyclic nucleotide-gated potassium channel 3	HCN3	57657	ENSG00000143630			Hcn3 (MGI:1298211)			
chr1	155289292	155301433	1q21	1q22		609712	"PKLR, PK1"	"Pyruvate kinase, liver and RBC type"	PKLR	5313	ENSG00000143627		"Adenosine triphosphate, elevated, of erythrocytes, 102900 (3), Autosomal dominant; Pyruvate kinase deficiency, 266200 (3), Autosomal recessive"	Pklr (MGI:97604)			
chr1	155308747	155320665	1q22	1q22		134629	"FDPS, FPS, POROK9"	Farnesyl diphosphate synthase	FDPS	2224	ENSG00000160752		"Porokeratosis 9, multiple types, 616631 (3), Autosomal dominant"	Fdps (MGI:104888)			
chr1	155320848	155331117	1q22	1q22		617318	"RUSC1, NESCA"	RUN domain- and SH3 domain-containing protein 1	RUSC1	23623	ENSG00000160753			Rusc1 (MGI:1919546)			
chr1	155335260	155563159	1q22	1q22		607999	"ASH1L, KIAA1420, ASH1, MRD52"	"ash1 (absent, small, or homeotic), Drosophila, homolog of"	ASH1L	55870	ENSG00000116539		"Mental retardation, autosomal dominant 52, 617796 (3), Autosomal dominant"	Ash1l (MGI:2183158)			
chr1	155610169	155614966	1q22	1q22		617619	"MSTO1, MMYAT"	"Misato 1, mitochondrial distribution and morphology regulator"	MSTO1	55154	ENSG00000125459		"Myopathy, mitochondrial, and ataxia, 617675 (3), Autosomal recessive, Autosomal dominant"	Msto1 (MGI:2385175)			
chr1	155659441	155689031	1q22	1q22		607860	"YY1AP1, YAP, HCCA2, GRNG"	YY1 associated protein 1	YY1AP1	55249	ENSG00000163374		"Grange syndrome, 602531 (3), Autosomal recessive"				
chr1	155687901	155739009	1q21	1q22		602074	DAP3	Death associated protein 3	DAP3	7818	ENSG00000132676			Dap3 (MGI:1929538)			
chr1	155749657	155859425	1q22	1q22		610393	"GON4L, KIAA1606"	GON4-like protein	GON4L	54856	ENSG00000116580			Gon4l (MGI:1917579)			
chr1	155897807	155911401	1q22	1q22		609591	"RIT1, RIT, ROC1, NS8"	Ric-like protein without CAAX motif 1	RIT1	6016	ENSG00000143622		"Noonan syndrome 8, 615355 (3), Autosomal dominant"	Rit1 (MGI:108053)			
chr1	155941688	155942833	1q22	1q22		609043	"RXFP4, RLN3R2, GPR100, GPCR142"	Relaxin/insulin-like family peptide receptor 4	RXFP4	339403	ENSG00000173080			Rxfp4 (MGI:2182926)			
chr1	155946838	155991261	1q21-q22	1q22		607560	"ARHGEF2, GEFH1, KIAA0651, NEDMHM"	RHO guanine nucleotide exchange factor 2	ARHGEF2	9181	ENSG00000116584	mutation identified in 1 NEDMHM family	"?Neurodevelopmental disorder with midbrain and hindbrain malformations, 617523 (3), Autosomal recessive"	Arhgef2 (MGI:103264)			
chr1	156009047	156020966	1q21-q23	1q22		600867	SSR2	"Signal sequence receptor, beta"	SSR2	6746	ENSG00000163479			Ssr2 (MGI:1913506)			
chr1	156033128	156053824	1q21	1q22		605440	"UBQLN4, A1U, C1orf6"	Ubiquitin 4	UBQLN4	56893	ENSG00000160803			Ubqln4 (MGI:2150152)			
chr1	156054725	156058509	1q22	1q22		610389	"LAMTOR2, MAPBPIP, p14"	"Late endosomal/lysosomal adaptor, MAPK and MTOR activator 2"	LAMTOR2	28956	ENSG00000116586		"Immunodeficiency due to defect in MAPBP-interacting protein, 610798 (3), Autosomal recessive"	Lamtor2 (MGI:1932697)			
chr1	156061148	156070513	1q22	1q22		612942	"RAB25, RAB11C"	Ras-associated protein RAB25	RAB25	57111	ENSG00000132698			Rab25 (MGI:1858203)			
chr1	156072012	156081997	1q22	1q22		611007	MEX3A	"Mex-3, C. elegans, homolog of, A"	MEX3A	92312	ENSG00000254726			Mex3a (MGI:1919890)			
chr1	156082545	156140088	1q21.2	1q22		150330	"LMNA, LMN1, EMD2, FPLD2, CMD1A, HGPS, LGMD1B"	Lamin A/C	LMNA	4000	ENSG00000160789		"Cardiomyopathy, dilated, 1A, 115200 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 2B1, 605588 (3), Autosomal recessive; Emery-Dreifuss muscular dystrophy 2, AD, 181350 (3), Autosomal dominant; Emery-Dreifuss muscular dystrophy 3, AR, 616516 (3), Autosomal recessive; Heart-hand syndrome, Slovenian type, 610140 (3), Autosomal dominant; Hutchinson-Gilford progeria, 176670 (3), Autosomal recessive, Autosomal dominant; Lipodystrophy, familial partial, type 2, 151660 (3), Autosomal dominant; Malouf syndrome, 212112 (3), Autosomal dominant; Mandibuloacral dysplasia, 248370 (3), Autosomal recessive; Muscular dystrophy, congenital, 613205 (3), Autosomal dominant; Muscular dystrophy, limb-girdle, type 1B, 159001 (3), Autosomal dominant; Restrictive dermopathy, lethal, 275210 (3), Autosomal recessive"	Lmna (MGI:96794)			
chr1	156149671	156177750	1q22	1q22		607292	"SEMA4A, SEMB, RP35, CORD10"	Semaphorin 4A	SEMA4A	64218	ENSG00000196189		"Cone-rod dystrophy 10, 610283 (3), Autosomal recessive; Retinitis pigmentosa 35, 610282 (3), Autosomal recessive, Autosomal dominant"	Sema4a (MGI:107560)			
chr1	156193931	156212795	1q22	1q22		610824	SLC25A44	"Solute carrier family 25, member 44"	SLC25A44	9673	ENSG00000160785			Slc25a44 (MGI:2444391)			
chr1	156212987	156240076	1q12	1q22		609176	PMF1	Polyamine-modulated factor 1	PMF1	11243	ENSG00000160783			Pmf1 (MGI:1914287)			
chr1	156241961	156243331	1q25-q31	1q22		112260	BGLAP	Bone gamma-carboxyglutamic acid protein	BGLAP	632	ENSG00000242252			"Bglap3,Bglap2,Bglap (MGI:88157,MGI:88155,MGI:88156)"			
chr1	156243320	156248521	1q22	1q22		614579	PAQR6	"Progestin and ADIPOQ receptor family, member 6"	PAQR6	79957	ENSG00000160781			Paqr6 (MGI:1916207)			
chr1	156249223	156291497	1q21.2	1q22		610962	"SMG5, EST1B, KIAA1089"	"SMG5, C. elegans, homolog of"	SMG5	23381	ENSG00000198952			Smg5 (MGI:2447364)			
chr1	156282912	156292442	1q23.1	1q22		615531	"TMEM79, MATT"	Transmembrane protein 79	TMEM79	84283	ENSG00000163472			Tmem79 (MGI:1919163)			
chr1	156308960	156338414	1q23	1q22		600114	"CCT3, TRIC5"	"Chaperonin-containing TCP1, subunit 3, gamma (TCP1 (t-complex-1) ring complex, polypeptide 5)"	CCT3	7203	ENSG00000163468			Cct3 (MGI:104708)			
chr1	156366043	156385220	1q21.3	1q22		607079	RHBG	"Rhesus blood group, B glycoprotein"	RHBG	57127	ENSG00000132677			Rhbg (MGI:1927379)			
chr1	156420340	156420428	1q22	1q22		611186	"MIR9-1, MIRN9-1"	Micro RNA 9-1	MIR9-1	407046							
chr1	156463720	156500841	1q12-q23	1q22		600663	MEF2D	"MADS box transcription enhancer factor 2, polypeptide D (myocyte enhancer factor 2D)"	MEF2D	4209	ENSG00000116604			Mef2d (MGI:99533)			
chr1	156591765	156599817	1q21	1q22		608862	"NAXE, APOA1BP, AIBP, PEBEL"	NAD(P)HX epimerase	NAXE	128240	ENSG00000163382		"Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 617186 (3), Autosomal recessive"	Naxe (MGI:2180167)			
chr1	156600000	165500000	1q23			605913	BDET	"Bleeding disorder, east Texas type"		85504			"Bleeding disorder, east Texas type, 605913 (2)"				
chr1	156600000	165500000	1q23			157560	"D1S61, D1S111, MS336"	Minisatellite 33.6		7824							
chr1	156641947	156659531	1q23.1	1q23.1		600347	BCAN	Brevican	BCAN	63827	ENSG00000132692			Bcan (MGI:1096385)			
chr1	156668762	156677396	1q23.1	1q23.1		600915	NES	Nestin	NES	10763	ENSG00000132688						
chr1	156699605	156705815	1q21.3	1q23.1		180231	"CRABP2, RBP6"	Cellular retinoic acid-binding protein-2	CRABP2	1382	ENSG00000143320			Crabp2 (MGI:88491)			
chr1	156721890	156728717	1q23.1	1q23.1		611930	ISG20L2	Interferon-stimulated exonuclease gene 20-kD-like 2	ISG20L2	81875	ENSG00000143319			Isg20l2 (MGI:2140076)			
chr1	156737301	156741266	1q21-q22	1q23.1		611836	MRPL24	Mitochondrial ribosomal protein L24	MRPL24	79590	ENSG00000143314			Mrpl24 (MGI:1914957)			
chr1	156742106	156752447	1q21	1q23.1		600339	HDGF	Hepatoma-derived growth factor	HDGF	3068	ENSG00000143321	previously assigned to Chr.X		Hdgf (MGI:1194494)			
chr1	156767481	156800818	1q21	1q23.1		179755	"PRCC, RCCP1"	"Papillary renal cell carcinoma, translocation-associated"	PRCC	5546	ENSG00000143294	t(X;1)(p11;q21); fuses with TFE3 in RCCP	"Renal cell carcinoma, papillary, 605074 (3)"	Prcc (MGI:2137738)			
chr1	156806237	156816852	1q21	1q23.1		604514	"SH2D2A, TSAD"	SH2 domain protein 2A	SH2D2A	9047	ENSG00000027869			Sh2d2a (MGI:1351596)			
chr1	156815749	156881849	1q21-q22	1q23.1		191315	"NTRK1, TRKA, MTC"	"Neurotrophic tyrosine kinase, receptor, type 1"	NTRK1	4914	ENSG00000198400	TRK = chimera of TPM3 and NTRK1	"Insensitivity to pain, congenital, with anhidrosis, 256800 (3), Autosomal recessive; Medullary thyroid carcinoma, familial, 155240 (3), Autosomal dominant"	Ntrk1 (MGI:97383)			
chr1	156840872	156858919	1q21-q23	1q23.1		147671	"INSRR, IRR"	Insulin receptor-related receptor	INSRR	3645	ENSG00000027644			Insrr (MGI:1346037)			
chr1	156893696	156916433	1q23.1	1q23.1		610278	PEAR1	Platelet endothelial aggregation receptor 1	PEAR1	375033	ENSG00000187800			Pear1 (MGI:1920432)			
chr1	157121190	157138590	1q21-q23	1q23.1		164873	"ETV3, PE1"	ets variant gene 3	ETV3	2117	ENSG00000117036			Etv3 (MGI:1350926)			
chr1	157513376	157552532	1q21	1q23.1		605877	IRTA2	Immunoglobulin superfamily receptor translocation-associated gene 2	FCRL5	83416	ENSG00000143297			Fcrl5 (MGI:3053558)			
chr1	157573748	157598079	1q21	1q23.1		605876	IRTA1	Immunoglobulin superfamily receptor translocation-associated gene 1	FCRL4	83417	ENSG00000163518	fused with IGHA1 in multiple myeloma					
chr1	157676480	157700984	1q21.2-q22	1q23.1		606510	FCRH3	Fc receptor-like protein 3	FCRL3	115352	ENSG00000160856						
chr1	157745732	157777471	1q21.2-q22	1q23.1		606509	"SPAP1, SPAP1A, SPAP1B, SPAP1C"	SH2 domain-containing phosphatase anchor protein 1	FCRL2	79368	ENSG00000132704						
chr1	157792248	157820149	1q21.2-q22	1q23.1		606508	"FCRL1, FCRH1"	Fc receptor-like protein 1	FCRL1	115350	ENSG00000163534			Fcrl1 (MGI:2442862)			
chr1	157827070	157841843	1q21-q23	1q23.1		602592	CD5L	CD5 antigen-like (scavenger receptor cysteine rich family)	CD5L	922	ENSG00000073754			Cd5l (MGI:1334419)			
chr1	157993272	158100261	1q23.1	1q23.1		607428	"KIRREL, NEPH1"	Kin of IRRE-like	KIRREL1	55243	ENSG00000183853			Kirrel (MGI:1891396)			
chr1	158178037	158186426	1q21-q23	1q23.1		188410	CD1D	Thymocyte antigen CD1D	CD1D	912	ENSG00000158473			Cd1d1 (MGI:107674)			
chr1	158248328	158258268	1q21-q23	1q23.1		188370	CD1A	Thymocyte antigen CD1A	CD1A	909	ENSG00000158477	"genes A, B, C, D in cluster"					
chr1	158285405	158331530	1q21-q23	1q23.1		188360	CD1B	Thymocyte antigen CD1B	CD1B	910	ENSG00000158485						
chr1	158289772	158294773	1q21-q23	1q23.1		188340	CD1C	Thymocyte antigen CD1C	CD1C	911	ENSG00000158481						
chr1	158353122	158357553	1q21-q23	1q23.1		188411	CD1E	Thymocyte antigen CD1E	CD1E	913	ENSG00000158488						
chr1	158610497	158686714	1q21	1q23.1		182860	"SPTA1, EL2, SPH3, HS3, HPP"	"Spectrin, alpha, erythrocytic-1"	SPTA1	6708	ENSG00000163554	17cM proximal to FY	"Elliptocytosis-2, 130600 (3), Autosomal dominant; Pyropoikilocytosis, 266140 (3), Autosomal recessive; Spherocytosis, type 3, 270970 (3), Autosomal recessive"	Spta1 (MGI:98385)			
chr1	158831302	158849503	1q22	1q23.1		159553	MNDA	Myeloid cell nuclear differentiation antigen	MNDA	4332	ENSG00000163563						
chr1	158931176	159010082	1q21-q23	1q23.1		612677	"PYHIN1, IFIX"	"Pyrin and Hin domain family, member 1"	PYHIN1	149628	ENSG00000163564						
chr1	158999969	159055154	1q22	1q23.1		147586	IFI16	"Interferon, gamma-inducible protein 16"	IFI16	3428	ENSG00000163565			"Ifi209,Ifi208,Ifi207,Ifi206,Ifi205,Ifi204,Ifi203,Ifi214,Ifi213,Ifi211,Mndal,Ifi203-ps (MGI:3041120,MGI:3584522,MGI:3780953,MGI:96429,MGI:96428,MGI:3695276,MGI:3646410,MGI:2442822,MGI:3840117,MGI:2138302,MGI:101847,MGI:2138243)"			
chr1	159059225	159132350	1q22	1q23.1-q23.2		604578	AIM2	Absent in melanoma 2	AIM2	9447	ENSG00000163568			Aim2 (MGI:2686159)			
chr1	159171563	159203312	1q21.2-q22	1q23.2		609743	"CADM3, IGSF4B, TSLL1, NECL1, SYNCAM3"	Cell adhesion molecule 3	CADM3	57863	ENSG00000162706			Cadm3 (MGI:2137858)			
chr1	159204012	159206499	1q23.2	1q23.2		613665	"ACKR1, DARC, FY, GPD, WBCQ1"	Atypical chemokine receptor 1 (Duffy antigen receptor for chemokines)	ACKR1	2532	ENSG00000213088	"by A, 1q22-q23"	"[Blood group, Duffy system], 110700 (3), Autosomal recessive, Autosomal dominant; {Malaria, vivax, protection against}, 611162 (3); [White blood cell count QTL], 611862 (3), Autosomal recessive"	Ackr1 (MGI:1097689)			
chr1	159283887	159308223	1q23	1q23.2		147140	FCER1A	"Fc IgE receptor, alpha polypeptide"	FCER1A	2205	ENSG00000179639			Fcer1a (MGI:95494)			
chr1	159587825	159588870	1q21-q23	1q23.2		104770	"APCS, SAP"	"Amyloid P component, serum"	APCS	325	ENSG00000132703	probably close to CRP	"{?Amyloidosis, secondary, susceptibility to} (1)"	Apcs (MGI:98229)			
chr1	159712288	159714588	1q21-q23	1q23.2		123260	CRP	C-reactive protein	CRP	1401	ENSG00000132693			Crp (MGI:88512)			
chr1	159826688	159837496	1q21	1q23.2		606620	"SLAMF8, BLAME"	"SLAM family, member 8"	SLAMF8	56833	ENSG00000158714			Slamf8 (MGI:1921998)			
chr1	159872363	159900115	1q22-q24	1q23.2		605152	"CCDC19, NESG1"	Coiled-coil domain-containing 19	CFAP45	25790	ENSG00000213085			Cfap45 (MGI:1919120)			
chr1	159918106	159925541	1q21-q25	1q23.2		604634	TAGLN2	Transgelin 2	TAGLN2	8407	ENSG00000158710			Tagln2 (MGI:1312985)			
chr1	159927038	159945660	1q22-q23	1q23.2		609738	"IGSF9, KIAA1355"	"Immunoglobulin superfamily, member 9"	IGSF9	57549	ENSG00000085552			Igsf9 (MGI:2135283)			
chr1	160027671	160031992	1q23.2	1q23.2		610273	PIGM	"Phosphatidylinositol glycan, class M"	PIGM	93183	ENSG00000143315		"Glycosylphosphatidylinositol deficiency, 610293 (3), Autosomal recessive"	Pigm (MGI:1914806)			
chr1	160037466	160070260	1q23.2	1q23.2		602208	"KCNJ10, SESAME"	"Potassium inwardly-rectifying channel, subfamily J, member 10"	KCNJ10	3766	ENSG00000177807		"Enlarged vestibular aqueduct, digenic, 600791 (3), Autosomal recessive; SESAME syndrome, 612780 (3), Autosomal recessive"	Kcnj10 (MGI:1194504)			
chr1	160055000	160090562	1q23.2	1q23.2		600932	"KCNJ9, GIRK3"	"Potassium inwardly-rectifying channel, subfamily J, member 9"	KCNJ9	3765	ENSG00000162728			Kcnj9 (MGI:108007)			
chr1	160091338	160099441	1q23.1	1q23.2		606644	"IGSF8, PGRL, CD81P3"	"Immunoglobulin superfamily, member 8"	IGSF8	93185	ENSG00000162729			Igsf8 (MGI:2154090)			
chr1	160115729	160143590	1q21-q23	1q23.2		182340	"ATP1A2, FHM2, MHP2"	"ATPase, Na+K+ transporting, alpha-2 polypeptide"	ATP1A2	477	ENSG00000018625		"Alternating hemiplegia of childhood 1, 104290 (3), Autosomal dominant; Migraine, familial basilar, 602481 (3), Autosomal dominant; Migraine, familial hemiplegic, 2, 602481 (3), Autosomal dominant"	Atp1a2 (MGI:88106)			
chr1	160151561	160186976	1q21-q32	1q23.2		607321	"ATP1A4, ATP1AL2"	"ATPase, Na+/K+ transporting, alpha-4 polypeptide"	ATP1A4	480	ENSG00000132681			Atp1a4 (MGI:1351335)			
chr1	160190494	160201885	1q21	1q23.2		114250	"CASQ1, VMCQA"	"Calsequestrin, fast-twitch, skeletal muscle-1"	CASQ1	844	ENSG00000143318		"Myopathy, vacuolar, with CASQ1 aggregates, 616231 (3), Autosomal dominant"	Casq1 (MGI:1309468)			
chr1	160205318	160215375	1q21.1	1q23.2		603434	"PEA15, HMAT1, PED"	"Phosphoprotein enriched in astrocytes, 15kD"	PEA15	8682	ENSG00000162734			Pea15a (MGI:104799)			
chr1	160215714	160262559	1q23.2	1q23.2		615820	"DCAF8, WDR42A, GAN2"	DDB1- and CUL4-associated factor 8	DCAF8	50717	ENSG00000132716	mutation identified in 1 GAN2 family	"?Giant axonal neuropathy 2, autosomal dominant, 610100 (3), Autosomal dominant"	Dcaf8 (MGI:91860)			
chr1	160276808	160285150	1q22	1q23.2		600279	"PEX19, PXF, HK33, D1S2223E, PBD12A"	Peroxisome biogenesis factor 19 (peroxisomal farnesylated protein)	PEX19	5824	ENSG00000162735		"Peroxisome biogenesis disorder 12A (Zellweger), 614886 (3), Autosomal recessive"	Pex19 (MGI:1334458)			
chr1	160288586	160343563	1q23-q25	1q23.2		601924	"COPA, AILJK"	"Coatomer protein complex, subunit alpha"	COPA	1314	ENSG00000122218		"{Autoimmune interstitial lung, joint, and kidney disease}, 616414 (3), Autosomal dominant"	Copa (MGI:1334462)			
chr1	160343272	160358951	1q22-q23	1q23.2		605254	NCSTN	Nicastrin	NCSTN	23385	ENSG00000162736		"Acne inversa, familial, 1, 142690 (3), Autosomal dominant"	Ncstn (MGI:1891700)			
chr1	160367070	160372847	1q22	1q23.2		162360	"NHLH1, HEN1"	Nescient helix loop helix 1	NHLH1	4807	ENSG00000171786	closely linked to Sap in mouse		Nhlh1 (MGI:98481)			
chr1	160400573	160428677	1q21-q23	1q23.2		600533	"VANGL2, LTAP"	"Vang-like 2 (loop-tail, mouse, homolog of)"	VANGL2	57216	ENSG00000162738		"Neural tube defects, 182940 (3), Autosomal dominant"	Vangl2 (MGI:2135272)			
chr1	160485029	160523262	1q23.1	1q23.2-q23.3		606446	"SLAMF6, NTBA"	"SLAM family, member 6"	SLAMF6	114836	ENSG00000162739			Slamf6 (MGI:1353620)			
chr1	160500000	165500000	1q23.3			610141	QTV	"QT interval, variation in"		100379215		associated with rs12143842	"[QT interval, variation in], 610141 (2)"				
chr1	160541093	160579515	1q23.3	1q23.3		604513	"CD84, SLAMF5"	CD84 antigen	CD84	8832	ENSG00000066294			Cd84 (MGI:1336885)			
chr1	160608099	160647310	1q22-q23	1q23.3		603492	"SLAMF1, SLAM, CDW150, CD150"	"SLAM family, member 1"	SLAMF1	6504	ENSG00000117090			Slamf1 (MGI:1351314)			
chr1	160678745	160711850	1q21.3-q22	1q23.3		109530	"CD48, BCM1, BLAST1"	CD48 antigen (B-cell membrane protein)	CD48	962	ENSG00000117091			Cd48 (MGI:88339)			
chr1	160739056	160754820	1q23-q24	1q23.3		606625	"SLAMF7, CRACC, CS1"	"SLAM family, member 7"	SLAMF7	57823	ENSG00000026751			Slamf7 (MGI:1922595)			
chr1	160796073	160828255	1q21.3-q22	1q23.3		600684	LY9	T-lymphocyte surface antigen Ly-9	LY9	4063	ENSG00000122224	within 410kb of CD48		Ly9 (MGI:96885)			
chr1	160830159	160862901	1q22	1q23.3		605554	"CD244, NAIL, NKR2B4, SLAMF4"	CD244 antigen	CD244	51744	ENSG00000122223		"{Rheumatoid arthritis, susceptibility to}, 180300 (3)"	Cd244 (MGI:109294)			
chr1	160876539	160885169	1q21.3-q22	1q23.3		609873	"ITLN1, INTL, LFR, HL1"	Intelectin 1	ITLN1	55600	ENSG00000179914			Itln1 (MGI:1333831)			
chr1	160945019	160957377	1q21.3-q22	1q23.3		609874	"ITLN2, HL2"	Intelectin 2	ITLN2	142683	ENSG00000158764						
chr1	160995205	161021342	1q21.2-q21.3	1q23.3		605721	"F11R, JAM1"	F11 receptor (junctional adhesion molecule 1)	F11R	50848	ENSG00000158769			F11r (MGI:1321398)			
chr1	161037630	161038983	1q23.3	1q23.3		616041	"TSTD1, KAT"	Thiosulfate sulfurtransferase (rhodanese)-like domain-containing protein 1	TSTD1	100131187	ENSG00000215845			Tstd1 (MGI:3648482)			
chr1	161039250	161045978	1q22-q23	1q23.3		191523	"USF1, HYPLIP1"	Upstream transcription factor 1	USF1	7391	ENSG00000158773		"{Hyperlipidemia, familial combined, susceptibility to}, 602491 (3)"	Usf1 (MGI:99542)			
chr1	161046941	161069970	1q23.3	1q23.3		614264	ARHGAP30	RHO GTPase-activating protein 30	ARHGAP30	257106	ENSG00000186517			Arhgap30 (MGI:2684948)			
chr1	161070990	161089594	1q23.3	1q23.3		609607	"NECTIN 4, PVRL4, PRR4, EDSS1"	Nectin 4	NECTIN4	81607	ENSG00000143217		"Ectodermal dysplasia-syndactyly syndrome 1, 613573 (3), Autosomal recessive"	Nectin4 (MGI:1918990)			
chr1	161098360	161100347	1q23.3	1q23.3		617375	"KLHDC9, KARCA1"	Kelch domain-containing protein 9	KLHDC9	126823	ENSG00000162755			Klhdc9 (MGI:1916124)			
chr1	161100555	161118075	1q23.3	1q23.3		613466	PFDN2	Prefoldin 2	PFDN2	5202	ENSG00000143256			Pfdn2 (MGI:1276111)			
chr1	161118071	161125445	1q21-q22	1q23.3		604618	NIT1	Nitrilase 1	NIT1	4817	ENSG00000158793			Nit1 (MGI:1350916)			
chr1	161120976	161132782	1q23.3	1q23.3		606841	"DEDD, DEFT"	Death effector domain-containing protein	DEDD	9191	ENSG00000158796			Dedd (MGI:1333874)			
chr1	161132702	161158855	1q23.3	1q23.3		610554	UFC1	Ubiquitin-fold modifier-conjugating enzyme 1	UFC1	51506	ENSG00000143222			Ufc1 (MGI:1913405)			
chr1	161159463	161165751	1q22	1q23.3		604729	"USP21, USP23"	Ubiquitin-specific protease 21	USP21	27005	ENSG00000143258			Usp21 (MGI:1353665)			
chr1	161165823	161178276	1q22	1q23.3		600923	PPOX	Protoporphyrinogen oxidase	PPOX	5498	ENSG00000143224		"Porphyria variegata, 176200 (3), Autosomal dominant"	Ppox (MGI:104968)			
chr1	161171309	161185006	1q23	1q23.3		604014	B4GALT3	"Beta-1,4-galactosyltransferase 3"	B4GALT3	8703	ENSG00000158850			B4galt3 (MGI:1928767)			
chr1	161189728	161202338	1q21-q23	1q23.3		603876	ADAMTS4	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 4 (aggrecanase 1)"	ADAMTS4	9507	ENSG00000158859			Adamts4 (MGI:1339949)			
chr1	161199314	161214394	1q23	1q23.3		602985	NDUFS2	"NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kD"	NDUFS2	4720	ENSG00000158864		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufs2 (MGI:2385112)			
chr1	161215296	161219247	1q23	1q23.3		147139	FCER1G	"Fc fragment of IgE, high affinity I, receptor for, gamma polypeptide"	FCER1G	2207	ENSG00000158869	probably on 1q close to CD32		Fcer1g (MGI:95496)			
chr1	161222292	161223627	1q21-q23	1q23.3		107670	APOA2	Apolipoprotein A-II	APOA2	336	ENSG00000158874		"Apolipoprotein A-II deficiency (3); {Hypercholesterolemia, familial, modifier of}, 143890 (3), Autosomal dominant"	Apoa2 (MGI:88050)			
chr1	161229665	161238622	1q23.1	1q23.3		603881	"NR1I3, CAR, MB67"	"Nuclear receptor subfamily 1, group I, member 3"	NR1I3	9970	ENSG00000143257			Nr1i3 (MGI:1346307)			
chr1	161303593	161309971	1q22	1q23.3		159440	"MPZ, CMT1B, CMTDID, CHM, DSS"	Myelin protein zero	MPZ	4359	ENSG00000158887		"Charcot-Marie-Tooth disease, dominant intermediate D, 607791 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 1B, 118200 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 2I, 607677 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 2J, 607736 (3), Autosomal dominant; Dejerine-Sottas disease, 145900 (3), Autosomal recessive, Autosomal dominant; Neuropathy, congenital hypomyelinating, 605253 (3), Autosomal recessive, Autosomal dominant; Roussy-Levy syndrome, 180800 (3), Autosomal dominant"	Mpz (MGI:103177)			
chr1	161314375	161364750	1q21	1q23.3		602413	"SDHC, PGL3"	"Succinate dehydrogenase complex, subunit C, integral membrane protein, 15kD"	SDHC	6391	ENSG00000143252		"Gastrointestinal stromal tumor, 606764 (3), Autosomal dominant, Isolated cases; Paraganglioma and gastric stromal sarcoma, 606864 (3); Paragangliomas 3, 605373 (3), Autosomal dominant"	Sdhc (MGI:1913302)			
chr1	161364730	161367882	1q23.3	1q23.3		616119	"CFAP126, FLTP"	Cilia- and flagella-associated protein 126	CFAP126	257177	ENSG00000188931			Cfap126 (MGI:1922722)			
chr1	161505414	161524047	1q21-q23	1q23.3		146790	"FCGR2A, IGFR2, CD32"	"Fc fragment of IgG, low affinity IIa, receptor for (CD32)"	FCGR2A	2212	ENSG00000143226	FCG2 and FCG3 within 250kb	"{Lupus nephritis, susceptibility to}, 152700 (3), Autosomal dominant; {Malaria, severe, susceptibility to}, 611162 (3); {Pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis}, 219700 (3), Autosomal recessive"	Fcgr3 (MGI:95500)			
chr1	161524539	161526896	1q	1q23.3		140555	HSPA6	Heat-shock 70kD protein-6 (HSP70B')	HSPA6	3310	ENSG00000173110						
chr1	161541758	161550736	1q23	1q23.3		146740	"FCGR3A, CD16, IGFR3, IMD20"	"Fc fragment of IgG, low affinity III, receptor for (CD16)"	FCGR3A	2214	ENSG00000203747	FCGR2A and FCGR3A within 250kb antigen	"Immunodeficiency 20, 615707 (3), Autosomal recessive"	Fcgr4 (MGI:2179523)			
chr1	161581338	161601219	1q23	1q23.3		612169	"FCGR2C, CD32C"	"Fc fragment of IgG, low affinity IIc, receptor for"	FCGR2C	9103	ENSG00000143226		"Thrombocytopenic purpura, autoimmune, 188030 (1), Autosomal dominant"				
chr1	161606058	161608550	1q	1q23.3		140556	HSPA7	Heat-shock 70kD protein-7 (HSP70B)	HSPA7	3311							
chr1	161623195	161631962	1q23	1q23.3		610665	FCGR3B	"Fc fragment of IgG, low affinity IIIb, receptor for"	FCGR3B	2215	ENSG00000162747		"Neutropenia, alloimmune neonatal (3)"	Fcgr4 (MGI:2179523)			
chr1	161647242	161678653	1q22	1q23.3		604590	"FCGR2B, CD32"	"Fc fragment of IgG, low affinity IIb, receptor for"	FCGR2B	2213	ENSG00000072694		"{Malaria, resistance to}, 611162 (3); {Systemic lupus erythematosus, susceptibility to}, 152700 (3), Autosomal dominant"	Fcgr2b (MGI:95499)			
chr1	161706971	161714351	1q23	1q23.3		606891	FREB	Fc receptor homolog expressed in B cells	FCRLA	84824	ENSG00000132185			Fcrla (MGI:2138647)			
chr1	161721543	161728142	1q23.3	1q23.3		609251	"FCRLB, FCRL2, FREB2, FCRY"	Fc receptor-like protein B	FCRLB	127943	ENSG00000162746			Fcrlb (MGI:3576487)			
chr1	161749767	161757163	1q21-q22	1q23.3		604835	"DUSP1, YVH1"	Dual-specificity phosphatase 12	DUSP12	11266	ENSG00000081721			Dusp12 (MGI:1890614)			
chr1	161766243	161964069	1q22-q23	1q23.3		605537	"ATF6, ACHM7"	Activating transcription factor-6	ATF6	22926	ENSG00000118217		"Achromatopsia 7, 616517 (3), Autosomal recessive"	Atf6 (MGI:1926157)			
chr1	162069790	162370022	1q23.3	1q23.3		605551	"NOS1AP, CAPON, KIAA0464"	Nitric oxide synthase 1 (neuronal) adaptor protein	NOS1AP	9722	ENSG00000198929						
chr1	162373724	162376961	1q23.3	1q23.3		617257	SPATA46	Spermatogenesis-associated protein 46	SPATA46	284680	ENSG00000171722			Spata46 (MGI:1924175)			
chr1	162395265	162412137	1q22	1q23.3		608510	"SH2D1B, EAT2"	SH2 domain-containing 1B	SH2D1B	117157	ENSG00000198574			Sh2d1b1 (MGI:1349420)			
chr1	162497173	162529628	1q23.1	1q23.3		608849	KIS	Kinase-interacting stathmin	UHMK1	127933	ENSG00000152332			Uhmk1 (MGI:1341908)			
chr1	162561439	162599842	1q23.3	1q23.3		602862	"UAP1, SPAG2"	ADP-N-acetylglucosamine pyrophosphorylase 1	UAP1	6675	ENSG00000117143			Uap1 (MGI:1334459)			
chr1	162631264	162786572	1q12-qter	1q23.3		191311	"DDR2, NTRKR3, TKT"	"Discoidin domain receptor family, member 2"	DDR2	4921	ENSG00000162733		"Spondylometaepiphyseal dysplasia, short limb-hand type, 271665 (3), Autosomal recessive"	Ddr2 (MGI:1345277)			
chr1	162790701	162812817	1q23.3	1q23.3		606756	HSD17B7	17-beta-hydroxysteroid dehydrogenase VII	HSD17B7	51478	ENSG00000132196			Hsd17b7 (MGI:1330808)			
chr1	163068605	163076801	1q23.3	1q23.3		602516	RGS4	Regulator of G protein signaling 4	RGS4	5999	ENSG00000117152			Rgs4 (MGI:108409)			
chr1	163142298	163321790	1q23	1q23.3		603276	RGS5	Regulator of G protein signaling-5	RGS5	8490	ENSG00000143248		"[Blood pressure regulation QTL], 145500 (2), Multifactorial"	Rgs5 (MGI:1098434)			
chr1	163321932	163355763	1q23	1q23.3		611772	"NUF2, NUF2R, CDCA1"	"NUF2, S. cerevisiae, homolog of"	NUF2	83540	ENSG00000143228			Nuf2 (MGI:1914227)			
chr1	164559359	164886046	1q23	1q23.3		176310	"PBX1, CAKUHED"	Pre-B cell leukemia transcription factor-1	PBX1	5087	ENSG00000185630	pseudogene PBXP1 on chr.3	"Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay, 617641 (3), Autosomal dominant"	Pbx1 (MGI:97495)			
chr1	165201866	165356714	1q22-q23	1q23.3		600298	"LMX1A, LMX1"	"LIM homeo box transcription factor-1, alpha"	LMX1A	4009	ENSG00000162761			Lmx1a (MGI:1888519)			
chr1	165400921	165445354	1q22-q23	1q23.3		180247	RXRG	"Retinoid X receptor, gamma"	RXRG	6258	ENSG00000143171			Rxrg (MGI:98216)			
chr1	165500000	173000000	1q24			605429	DFNM1	"Deafness, nonsyndromic, modifier 1"	DFNM1	54362			"{Deafness, nonsyndromic, modifier 1}, 605429 (2)"				
chr1	165544240	165563947	1q24.1	1q24.1		615218	LRRC52	Leucine-rich repeat-containing protein 52	LRRC52	440699	ENSG00000162763			Lrrc52 (MGI:1924118)			
chr1	165630872	165656135	1q23	1q24.1		604564	MGST3	"Glutatione S-transferase, microsomal, 3"	MGST3	4259	ENSG00000143198			Mgst3 (MGI:1913697)			
chr1	165662211	165698662	1q22-q23	1q24.1		602733	"ALDH9A1, ALDH9, E3"	"Aldehyde dehydrogenase 9 family, member A1"	ALDH9A1	223	ENSG00000143149			Aldh9a1 (MGI:1861622)			
chr1	165724290	165768921	1q24.1	1q24.1		614123	"TMCO1, CFSMR"	Transmembrane and coiled-coil domains protein 1	TMCO1	54499	ENSG00000143183		"Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome, 213980 (3), Autosomal recessive"	Tmco1 (MGI:1921173)			
chr1	165827494	165911617	1q22-q23.2	1q24.1		609329	"UCK2, TSA903"	Uridine/cytidine kinase 2	UCK2	7371	ENSG00000143179			Uck2 (MGI:1931744)			
chr1	166856509	166876416	1q24-q25	1q24.1		612763	"TADA1L, STAF42"	Transcriptional adaptor 1-like	TADA1	117143	ENSG00000152382			Tada1 (MGI:1196415)			
chr1	166921120	167022213	1q24.1	1q24.1		611368	MAEL	"Maelstrom, Drosophila, homolog of"	MAEL	84944	ENSG00000143194			Mael (MGI:2138453)			
chr1	167052835	167090630	1q24.1	1q24.1		602171	GPA33	Glycoprotein A33	GPA33	10223	ENSG00000143167			Gpa33 (MGI:1891703)			
chr1	167220828	167427344	1q22-q23	1q24.2		164175	"OTF1, OCT1"	Octamer-binding transcription factor-1	POU2F1	5451	ENSG00000143190			Pou2f1 (MGI:101898)			
chr1	167430639	167518609	1q22-q23	1q24.2		186780	"CD247, CD3Z, TCRZ, IMD25"	CD247 antigen	CD247	919	ENSG00000198821	mutation identified in one IMD25 patient	"?Immunodeficiency 25, 610163 (3), Autosomal recessive"	Cd247 (MGI:88334)			
chr1	167630192	167708695	1q24	1q24.2		610579	"RCSD1, CAPZIP"	RCSD domain-containing protein 1	RCSD1	92241	ENSG00000198771			Rcsd1 (MGI:2676394)			
chr1	167721949	167791918	1q24	1q24.2		604376	"MPZL1, PZR"	Myelin protein zero-like 1	MPZL1	9019	ENSG00000197965			Mpzl1 (MGI:1915731)			
chr1	167809079	167916388	1q24	1q24.2		605205	"ADCY10, SAC, HCA2"	"Adenylyl cyclase 10, soluble"	ADCY10	55811	ENSG00000143199		"{Hypercalciuria, absorptive, susceptibility to}, 143870 (3), Autosomal dominant"	Adcy10 (MGI:2660854)			
chr1	167916674	167937068	1q24.2	1q24.2		614737	"BRP44, MPC2"	Brain protein 44	MPC2	25874	ENSG00000143158			Mpc2 (MGI:1917706)			
chr1	167936238	168075842	1q24.2	1q24.2		610494	"DCAF6, IQWD1, NRIP"	DDB1 and CUL4 associated factor 6	DCAF6	55827	ENSG00000143164			Dcaf6 (MGI:1921356)			
chr1	168079541	168137666	1q24.2	1q24.2		612250	GPR161	G protein-coupled receptor 161	GPR161	23432	ENSG00000143147			Gpr161 (MGI:2685054)			
chr1	168178844	168202113	1q23.2	1q24.2		611807	"TIPRL, TIP41, TIP"	TIP41-like protein	TIPRL	261726	ENSG00000143155			Tiprl (MGI:1915087)			
chr1	168281039	168314425	1q23-q24	1q24.2		604614	TBX19	T-box 19	TBX19	9095	ENSG00000143178		"Adrenocorticotropic hormone deficiency, 201400 (3), Autosomal recessive"	Tbx19 (MGI:1891158)			
chr1	168540764	168543996	1q23	1q24.2		604828	"XCL2, SCYC2, SCM1B"	"Chemokine, C motif, ligand 2"	XCL2	6846	ENSG00000143185						
chr1	168574127	168582076	1q23	1q24.2		600250	"XCL1, SCYC1, SCM1, LTN, LPTN"	"Chemokine, C motif, ligand 1 (lymphotactin)"	XCL1	6375	ENSG00000143184			Xcl1 (MGI:104593)			
chr1	168695456	168729203	1q12-q23	1q24.2		125597	DPT	Dermatopontin	DPT	1805	ENSG00000143196			Dpt (MGI:1928392)			
chr1	169106708	169132721	1q22-q25	1q24.2		182330	ATP1B1	"ATPase, Na+K+ transporting, beta-1 polypeptide"	ATP1B1	481	ENSG00000143153		"[Blood pressure regulation QTL], 145500 (2), Multifactorial"	Atp1b1 (MGI:88108)			
chr1	169132529	169367962	1q24	1q24.2		613465	"NME7, MN23H7"	"Nonmetastatic cells 7, protein expressed in"	NME7	29922	ENSG00000143156			Nme7 (MGI:2449121)			
chr1	169463908	169485969	1q23.3	1q24.2		603941	"SLC19A2, THTR1, TRMA, THMD1"	"Solute carrier family 19 (thiamine transporter), member 2"	SLC19A2	10560	ENSG00000117479		"Thiamine-responsive megaloblastic anemia syndrome, 249270 (3), Autosomal recessive"	Slc19a2 (MGI:1928761)			
chr1	169511953	169586629	1q23	1q24.2		612309	"F5, THPH2, RPRGL1"	"Coagulation factor V (proaccelerin, labile factor)"	F5	2153	ENSG00000198734	Order: F5-GRMP-LYAM1-ELAM1 in 300kb segment	"{Budd-Chiari syndrome}, 600880 (3), Autosomal recessive; Factor V deficiency, 227400 (3), Autosomal recessive; {Pregnancy loss, recurrent, susceptibility to, 1}, 614389 (3), Autosomal dominant; {Stroke, ischemic, susceptibility to}, 601367 (3), Multifactorial; Thrombophilia due to activated protein C resistance, 188055 (3), Autosomal dominant; {Thrombophilia, susceptibility to, due to factor V Leiden}, 188055 (3), Autosomal dominant"	F5 (MGI:88382)			
chr1	169588848	169630138	1q23-q25	1q24.2		173610	"SELP, GRMP"	"Selectin P (granulocyte membrane protein, 140kD; antigen CD62)"	SELP	6403	ENSG00000174175	"in same 300kb segment as LYAM1, ELAM1"		Selp (MGI:98280)			
chr1	169690664	169711701	1q23-q25	1q24.2		153240	"SELL, LYAM1, LAM1, LNHR"	Selectin L (lymphocyte adhesion molecule 1)	SELL	6402	ENSG00000188404			Sell (MGI:98279)			
chr1	169722639	169734078	1q23-q25	1q24.2		131210	"SELE, ELAM1"	Selectin E (endothelial leukocyte adhesion molecule-1)	SELE	6401	ENSG00000007908			Sele (MGI:98278)			
chr1	169792523	169794975	1q24.2	1q24.2		615255	"METTL18, C1orf156"	Methyltransferase-like 18	METTL18	92342	ENSG00000171806			Mettl18 (MGI:1917212)			
chr1	169853073	169894266	1q24.2	1q24.2		608192	"SCYL3, PACE1"	"SCY1-like 3, S. cerevisiae, homolog of"	SCYL3	57147	ENSG00000000457			Scyl3 (MGI:1921385)			
chr1	169921325	170085202	1q24.2	1q24.2		601836	"KIFAP3, SMAP"	Kinesin-associated protein 3	KIFAP3	22920	ENSG00000075945			Kifap3 (MGI:107566)			
chr1	170532121	170553833	1q24.2	1q24.2		607983	"GORAB, SCYL1BP1, NTKLBP1, GO"	"Golgin, RAB6-interacting"	GORAB	92344	ENSG00000120370		"Geroderma osteodysplasticum, 231070 (3), Autosomal recessive"	Gorab (MGI:2138271)			
chr1	170662727	170739399	1q24	1q24.2		167420	"PRRX1, PMX1, PHOX1, AGOTC"	Paired-related homeobox gene 1	PRRX1	5396	ENSG00000116132		"Agnathia-otocephaly complex, 202650 (3), Autosomal recessive, Autosomal dominant"	Prrx1 (MGI:97712)			
chr1	171090872	171117818	1q23-q25	1q24.3		136132	"FMO3, TMAU"	Flavin-containing monooxygenase 3	FMO3	2328	ENSG00000007933		"Trimethylaminuria, 602079 (3), Autosomal recessive"	Fmo3 (MGI:1100496)			
chr1	171185207	171212682	1q23-q25	1q24.3		603955	FMO2	"Flavin-containing monooxygenase 2, pulmonary"	FMO2	2327	ENSG00000094963	probably cluster of FMO genes at 1q23-q25		Fmo2 (MGI:1916776)			
chr1	171248470	171285977	1q23-q25	1q24.3		136130	FMO1	"Flavin-containing monooxygenase 1, fetal liver"	FMO1	2326	ENSG00000010932			Fmo1 (MGI:1310002)			
chr1	171314130	171342083	1q23-q25	1q24.3		136131	FMO4	"Flavin-containing monooxygenase 2, adult liver"	FMO4	2329	ENSG00000076258			Fmo4 (MGI:2429497)			
chr1	171485495	171593510	1q24.3	1q24.3		617373	"PRRC2C, KIAA1096"	Proline-rich coiled-coil protein 3C	PRRC2C	23215	ENSG00000117523			Prrc2c (MGI:1913754)			
chr1	171635416	171652632	1q24.3-q25.2	1q24.3		601652	"MYOC, TIGR, GLC1A, JOAG, GPOA"	Myocilin (trabecular meshwork-induced glucocorticoid response protein)	MYOC	4653	ENSG00000034971		"Glaucoma 1A, primary open angle, 137750 (3), Autosomal dominant"	Myoc (MGI:1202864)			
chr1	171700155	171742843	1q24-q25	1q24.3		606909	VAMP24	Vesicle-associated membrane protein 4	VAMP4	8674	ENSG00000117533			Vamp4 (MGI:1858730)			
chr1	171841477	172418465	1q24.3	1q24.3		611445	"DNM3, KIAA0820"	Dynamin 3	DNM3	26052	ENSG00000197959			Dnm3 (MGI:1341299)			
chr1	172138797	172138906	1q24.3	1q24.3		610721	"MIR214, MIRN214"	Micro RNA 214	MIR214	406996							
chr1	172138807	172138887	1q24.3	1q24.3		614722	MIR3120	Micro RNA 3120	MIR3120	100422882		in intron 13 of DNM3 in sense orientation					
chr1	172144534	172144643	1q24.3	1q24.3		610720	"MIR199A2, MIRN199A2"	Micro RNA 199A2	MIR199A2	406977							
chr1	172441456	172444089	1q23-q25	1q24.3		601730	"PIGC, GPI2, GPIBD16, MRT62"	"Phosphatidylinositol glycan, class C"	PIGC	5279	ENSG00000135845		"Glycosylphosphatidylinositol biosynthesis defect 16, 617816 (3)"	Pigc (MGI:1914542)			
chr1	172659007	172666872	1q23	1q24.3		134638	"FASLG, TNFSF6, APT1LG1, FASL, ALPS1B"	"Fas ligand (TNF superfamily, member 6)"	FASLG	356	ENSG00000117560		"Autoimmune lymphoproliferative syndrome, type IB, 601859 (3), Autosomal dominant; {Lung cancer, susceptibility to}, 211980 (3), Autosomal recessive"	Fasl (MGI:99255)			
chr1	173000000	185800000	1q25			611154	AD14	Alzheimer disease 14		100188754		max lod at D1S218	"{Alzheimer disease-14}, 611154 (2)"				
chr1	173000000	185800000	1q25			608526	PDON2	"Periodontitis, aggressive, 2"		406237		between D1S196 and D1S533	"Periodontitis, aggressive, 2, 608526 (2)"				
chr1	173000000	185800000	1q25			611013	RGSL2	Regulator of G protein signaling-like 2				related to AD linked to 1q25					
chr1	173041219	173050962	1q23	1q25.1		603898	"TNFSF18, AITRL, GITRL"	"Tumor necrosis factor ligand superfamily, member 18"	TNFSF18	8995	ENSG00000120337			Tnfsf18 (MGI:2673064)			
chr1	173183728	173462207	1q25	1q25.1		603594	"TNFSF4, GP34, OX4OL"	"Tumor necrosis factor ligand superfamily, member 4"	TNFSF4	7292	ENSG00000117586		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Tnfsf4 (MGI:104511)			
chr1	173477346	173488806	1q25.1	1q25.1		602316	PRDX6	Peroxiredoxin 6	PRDX6	9588	ENSG00000117592			Prdx6 (MGI:894320)			
chr1	173714911	173786825	1q25.1	1q25.1		617679	"KLHL20, KLEIP, KLHLX"	Kelch-like 20	KLHL20	27252	ENSG00000076321			Klhl20 (MGI:2444855)			
chr1	173799549	173824638	1q25.1	1q25.1		611503	CENPL	Centromeric protein L	CENPL	91687	ENSG00000120334			Cenpl (MGI:1917704)			
chr1	173824646	173858543	1q25.1	1q25.1		610956	"DARS2, ASPRS. LBSL"	Aspartyl-tRNA synthetase 2	DARS2	55157	ENSG00000117593		"Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation, 611105 (3), Autosomal recessive"	Dars2 (MGI:2442510)			
chr1	173863898	173868881	1q23.3	1q25.1		608280	GAS5	Growth arrest-specific 5	GAS5	60674							
chr1	173903803	173917377	1q23-q25	1q25.1		107300	"SERPINC1, AT3, AT3D, THPH7"	Antithrombin III	SERPINC1	462	ENSG00000117601	~17cM distal to FY	"Thrombophilia due to antithrombin III deficiency, 613118 (3), Autosomal recessive, Autosomal dominant"	Serpinc1 (MGI:88095)			
chr1	173931083	173993071	1q25.1	1q25.1		609424	"RC3H1, KIAA2025"	Roquin	RC3H1	149041	ENSG00000135870			Rc3h1 (MGI:2685397)			
chr1	174448073	174449544	1q24	1q25.1		604106	GPR52	G protein-coupled receptor 52	GPR52	9293	ENSG00000203737			Gpr52 (MGI:3643278)			
chr1	174999434	175012026	1q24-q25	1q25.1		606186	SIP	SIAH1-interacting protein	CACYBP	27101	ENSG00000116161			Cacybp (MGI:1270839)			
chr1	175012957	175023454	1q23-q25	1q25.1		611978	MRPS14	Mitochondrial ribosomal protein S14	MRPS14	63931	ENSG00000120333			Mrps14 (MGI:1928141)			
chr1	175067857	175148065	1q25.1	1q25.1		617472	TNN	Tenascin N	TNN	63923	ENSG00000120332			Tnn (MGI:2665790)			
chr1	175156985	175193294	1q25.1	1q25.1		616696	KIAA0040	KIAA0040 gene	KIAA0040	9674	ENSG00000235750			4930523C07Rik (MGI:1914897)			
chr1	175320780	175743701	1q24	1q25.1		601995	TNR	"Tenascin R (restrictin, janusin)"	TNR	7143	ENSG00000116147			Tnr (MGI:99516)			
chr1	175944825	176209086	1q24.1	1q25.1-q25.2		608067	"RFWD2, COP1"	Ring finger- and WD repeat domain-containing protein 2	COP1	64326	ENSG00000143207	"pseudogenes on chr. 3, 9, 18"		Cop1 (MGI:1347046)			
chr1	176100000	185800000	1q25.2-q25.3			615492	LINC-COX2	Long intergenic noncoding RNA COX2									
chr1	176855116	177164903	1q25	1q25.2		600904	"ASTN1, ASTN"	Astrotactin 1	ASTN1	460	ENSG00000152092			Astn1 (MGI:1098567)			
chr1	177928787	177984302	1q25.2	1q25.2		612855	"SEC16B, LZTR2, RGPR, SEC16S"	"Sec16, S. cerevisiae, homolog of, B"	SEC16B	89866	ENSG00000120341			Sec16b (MGI:2148802)			
chr1	178093728	178479513	1q25.2	1q25.2		606136	"RASAL2, NGAP"	Ras protein activator-like 2	RASAL2	9462	ENSG00000075391			Rasal2 (MGI:2443881)			
chr1	178725146	178921841	1q25.2	1q25.2		617819	"RALGPS2, FLJ10244"	RAL guanine nucleotide exchange factor with PH domain and SH3 domain-binding motif 2	RALGPS2	55103	ENSG00000116191			Ralgps2 (MGI:1925505)			
chr1	179025803	179076573	1q25	1q25.2		611063	FAM20B	"Family with sequence similarity 20, member B"	FAM20B	9917	ENSG00000116199			Fam20b (MGI:2443990)			
chr1	179081976	179095995	1q25-q31	1q25.2		607555	"TOR3A, ADIR"	"Torsin family 3, member A (ATP-dependent interferon-responsive protein)"	TOR3A	64222	ENSG00000186283			Tor3a (MGI:1353652)			
chr1	179099326	179229692	1q24-q25	1q25.2		164690	"ABL2, ABLL, ARG"	"Abelson murine leukemia viral (v-abl) oncogene homolog 2 (arg, Abelson-related gene)"	ABL2	27	ENSG00000143322	fused with ETV6 in AML	"Leukemia, acute myeloid, with eosinophilia (1)"	Abl2 (MGI:87860)			
chr1	179293713	179358679	1q25	1q25.2		102642	"SOAT1, STAT, ACAT"	Sterol O-acyltransferase 1 (acyl-Coenzyme A: cholesterol acyltransferase 1)	SOAT1	6646	ENSG00000057252			Soat1 (MGI:104665)			
chr1	179550538	179575986	1q25-q31	1q25.2		604766	"PDCN, NPHS2, SRN1"	Podocin	NPHS2	7827	ENSG00000116218	modifies phenotype of NPHS1 mutations to FSGS	"Nephrotic syndrome, type 2, 600995 (3), Autosomal recessive"	Nphs2 (MGI:2157018)			
chr1	179591612	179691271	1q25.2	1q25.2		617748	"TDRD5, TUDOR3"	Tudor domain-containing protein 5	TDRD5	163589	ENSG00000162782			Tdrd5 (MGI:2684949)			
chr1	179727762	179816197	1q24.3	1q25.2		611727	"C1orf76, NDSP"	Neuroblastoma-derived secretory protein	FAM163A	148753	ENSG00000143340			Fam163a (MGI:3618859)			
chr1	179839966	179877805	1q24	1q25.2		614513	"TOR1AIP2, LULL1"	Torsin A-interacting protein 2	TOR1AIP2	163590	ENSG00000169905			Tor1aip2 (MGI:3582695)			
chr1	179882041	179920076	1q24	1q25.2		614512	"TOR1AIP1, LAP1, LAP1B, LGMD2Y"	Torsin A-interacting protein 1	TOR1AIP1	26092	ENSG00000143337	mutation identified in 1 LGMD2Y family	"?Muscular dystrophy, limb-girdle, type 2Y, 617072 (3), Autosomal recessive"	Tor1aip1 (MGI:3582693)			
chr1	179954772	180114879	1q25.2	1q25.2		617870	"CEP350, CAP350, KIAA0480"	Centrosomal protein 350	CEP350	9857	ENSG00000135837			Cep350 (MGI:1921331)			
chr1	180154832	180198033	1q24	1q25.2		603120	QSOX1	Quiescin Q6 sulfhydryl oxidase 1	QSOX1	5768	ENSG00000116260			Qsox1 (MGI:1330818)			
chr1	180228371	180278981	1q25	1q25.2		602146	"LHX4, CPHD4"	LIM homeo box gene 4	LHX4	89884	ENSG00000121454	fused to IGH in ALL	"Pituitary hormone deficiency, combined, 4, 262700 (3), Autosomal dominant"	Lhx4 (MGI:101776)			
chr1	180269662	180502886	1q25.3-q25.3	1q25.2-q25.3		616352	ACBD6	Acyl-CoA-binding domain-containing protein 6	ACBD6	84320	ENSG00000230124			Acbd6 (MGI:1919732)			
chr1	180434795	180436801	1q25.3	1q25.3		610030	VDAC4	Voltage-dependent anion channel 4	VDAC1P4	7418							
chr1	180632009	180890278	1q25.1	1q25.3		605237	"XPR1, SYG1, IBGC6"	Xenotropic and polytropic retrovirus receptor	XPR1	9213	ENSG00000143324		"Basal ganglia calcification, idiopathic, 6, 616413 (3), Autosomal dominant"	Xpr1 (MGI:97932)			
chr1	180972711	181023120	1q25.3	1q25.3		603944	STX6	Syntaxin 6	STX6	10228	ENSG00000135823			Stx6 (MGI:1926235)			
chr1	181033391	181061937	1q25.3	1q25.3		600764	"MR1, HLALS"	"Major histocompatibility complex, class I-related"	MR1	3140	ENSG00000153029			Mr1 (MGI:1195463)			
chr1	181088501	181090842	1q25.3	1q25.3		607177	IER5	Immediate-early response gene 5	IER5	51278	ENSG00000162783			Ier5 (MGI:1337072)			
chr1	181317711	181808083	1q25-q31	1q25.3		601013	"CACNA1E, CACNL1A6"	"Calcium channel, voltage-dependent, alpha 1E subunit"	CACNA1E	777	ENSG00000198216			Cacna1e (MGI:106217)			
chr1	182378092	182392205	1q31	1q25.3		138290	"GLUL, GLNS"	Glutamate-ammonia ligase (glutamine synthase)	GLUL	2752	ENSG00000135821	pseudogene on chr.9	"Glutamine deficiency, congenital, 610015 (3), Autosomal recessive"	Glul (MGI:95739)			
chr1	182447875	182560596	1q25	1q25.3		611012	RGSL1	Regulator of G protein signaling-like 1	RGSL1	353299	ENSG00000121446			Rgsl1 (MGI:2685048)			
chr1	182573633	182589284	1q25	1q25.3		180435	"RNASEL, RNS4, PRCA1, HPC1"	"Ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)"	RNASEL	6041	ENSG00000135828		"Prostate cancer 1, 601518 (3), Autosomal dominant"	Rnasel (MGI:1098272)			
chr1	182598622	182604412	1q25-q31	1q25.3		602514	RGS16	Regulator of G protein signaling-16	RGS16	6004	ENSG00000143333			Rgs16 (MGI:108407)			
chr1	182789448	182830383	1q25	1q25.3		611412	"NPL, C1orf13, C112"	N-acetylneuraminate pyruvate lyase	NPL	80896	ENSG00000135838			Npl (MGI:1921341)			
chr1	182839303	182887981	1q25	1q25.3		603115	"DHX9, DDX9, NDHII"	DEAH (Asp-Glu-Ala-His) box polypeptide 9	DHX9	1660	ENSG00000135829			Dhx9 (MGI:108177)			
chr1	183023459	183145591	1q31	1q25.3		150290	"LAMC1, LAMB2"	"Laminin, gamma-1 (formerly LAMB2)"	LAMC1	3915	ENSG00000135862	"at least 3 genes, ?linked"		Lamc1 (MGI:99914)			
chr1	183186038	183245126	1q25-q31	1q25.3		150292	"LAMC2, LAMNB2, LAMB2T"	"Laminin, gamma-2 (nicein, 100kD; kalinin, 105kD; BM600, 100kD)"	LAMC2	3918	ENSG00000058085		"Epidermolysis bullosa, junctional, Herlitz type, 226700 (3), Autosomal recessive; Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3), Autosomal recessive"	Lamc2 (MGI:99913)			
chr1	183248236	183418498	1q25.3	1q25.3		608701	"NMNAT2, PNAT2, KIAA0479"	Nicotinamide nucleotide adenylyltransferase 2	NMNAT2	23057	ENSG00000157064			Nmnat2 (MGI:2444155)			
chr1	183471992	183554192	1q25	1q25.3		610964	"SMG7, EST1C, KIAA0250"	"SMG7, C. elegans, homolog of"	SMG7	9887	ENSG00000116698			Smg7 (MGI:2682334)			
chr1	183555561	183590920	1q25	1q25.3		608515	NCF2	"Neutrophil cytosolic factor-2, 65kD"	NCF2	4688	ENSG00000116701		"Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3), Autosomal recessive"	Ncf2 (MGI:97284)			
chr1	183626192	183635940	1q25.3	1q25.3		604227	"ARPC5, ARC16"	"Actin-related protein 2/3 complex, subunit 5"	ARPC5	10092	ENSG00000162704			Arpc5 (MGI:1915021)			
chr1	183636046	183928550	1q25.3	1q25.3		605667	"RGL1, RGL"	Ral guanine nucleotide dissociation stimulator-like 1	RGL1	23179	ENSG00000143344			Rgl1 (MGI:107484)			
chr1	183646274	183653312	1q25.3	1q25.3		609908	APOBEC4	"Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 4"	APOBEC4	403314	ENSG00000173627			Apobec4 (MGI:1918531)			
chr1	184051650	184095845	1q25	1q25.3		608756	"TSEN15, SEN15, C1orf19, PCH2F"	"tRNA splicing endonuclease 15, S. cerevisiae, homolog of"	TSEN15	116461	ENSG00000198860		"Pontocerebellar hypoplasia, type 2F, 617026 (3), Autosomal recessive"	Tsen15 (MGI:1913887)			
chr1	185045418	185102607	1q25.3	1q25.3		608985	"RNF2, RING2, RING1B, HIPI3, DING, BAP1"	RING finger protein 2	RNF2	6045	ENSG00000121481			Rnf2 (MGI:1101759)			
chr1	185118084	185157097	1q25	1q25.3		611673	"TRMT1L, C1orf25, TRM1L"	tRNA methyltransferase 1-like	TRMT1L	81627	ENSG00000121486			Trmt1l (MGI:1916185)			
chr1	185292366	185317328	1q25.3	1q25.3		609209	"IVNS1ABP, NS1BP, ND1"	Influenza virus NS1A protein-binding protein	IVNS1ABP	10625	ENSG00000116679			Ivns1abp (MGI:2152389)			
chr1	185734524	186190952	1q24-q25	1q25.3-q31.1		608548	"HMCN1, FBLN6, FIBL6, ARMD1"	Hemicentin (fibulin 6)	HMCN1	83872	ENSG00000143341		"{Macular degeneration, age-related, 1}, 603075 (3), Autosomal dominant"	Hmcn1 (MGI:2685047)			
chr1	185800000	198700000	1q31			120502	BOS2	Branchiootic syndrome 2		64585			"Branchiootic syndrome 2, 120502 (2), Autosomal dominant"				
chr1	185800000	198700000	1q31			612005	CELIAC7	"Celiac disease, susceptibility to, 7"		100301522		associated with rs2816316	"{Celiac disease, susceptibility to, 7}, 612005 (2)"				
chr1	185800000	198700000	1q31			607516	"MGR6, FHM3"	"Migraine, several forms"		317773			"{Migraine with or without aura, susceptibility to, 6}, 607516 (2), Autosomal dominant; {Migraine, familial hemiplegic, 4}, 607516 (2), Autosomal dominant"				
chr1	185800000	236400000	1q31-q42			145260	"PHA2A, PHA2"	Pseudohypoaldosteronism type IIA		7830			"Pseudohypoaldosteronism, type IIA, 145260 (2), Autosomal dominant"				
chr1	185800000	190800000	1q31.1			609454	PSNP2	"Supranuclear palsy, progressive, 2"		619408		between D1S238 and D1S2823	"Supranuclear palsy, progressive, 2, 609454 (2), Autosomal dominant"				
chr1	185800000	198700000	1q31			176780	PVOP1	"Pelvic organ prolapse, susceptibility to, 1"		100312952		associated with rs10911193	"{Pelvic organ prolapse, susceptibility to, 1}, 176780 (2), Autosomal dominant"				
chr1	186296272	186314561	1q24-q25	1q31.1		604283	"PRG4, CACP, MSF, SZP, HAPO"	Proteoglycan 4 (megakaryocyte stimulating factor; hemangiopoietin)	PRG4	10216	ENSG00000116690		"Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3), Autosomal recessive"				
chr1	186311651	186375324	1q25	1q31.1		189940	TPR	Tumor potentiating region (translocated promoter region)	TPR	7175	ENSG00000047410	fused with MET in chemically induced tumor		Tpr (MGI:1922066)			
chr1	186443565	186461107	1q25-q31.1	1q31.1		171490	PDC	"Phosducin, pineal gland"	PDC	5132	ENSG00000116703			Pdc (MGI:98090)			
chr1	186671811	186680426	1q25.2-q25.3	1q31.1		600262	PTGS2	Prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)	PTGS2	5743	ENSG00000073756			Ptgs2 (MGI:97798)			
chr1	186680653	186681445	1q31.1	1q31.1		617650	"PACERR, PTGS2AS1"	"PTGS2 antisense NFKB1 complex-mediated expression regulator RNA, noncoding"	PACERR	103752588							
chr1	186828899	186988980	1q25	1q31.1		600522	"PLA2G4A, PLA2G4"	"Phospholipase A2, group IVA, cytosolic"	PLA2G4A	5321	ENSG00000116711		"Phospholipase A2, group IV A, deficiency of (3)"	Pla2g4a (MGI:1195256)			
chr1	192316991	192367284	1q31.2	1q31.2		612407	RGS21	Regulator of G protein signaling 21	RGS21	431704	ENSG00000253148			Rgs21 (MGI:3645243)			
chr1	192575726	192580028	1q31	1q31.2		600323	"RGS1, IER1, IR20"	Regulator of G-protein signaling 1	RGS1	5996	ENSG00000090104			Rgs1 (MGI:1354694)			
chr1	192809038	192812276	1q31	1q31.2		600861	"RGS2, G0S8"	"G0 to G1 switch regulatory 8, 24kD"	RGS2	5997	ENSG00000116741			Rgs2 (MGI:1098271)			
chr1	193012252	193060139	1q32	1q31.2		610667	"UCHL5, UCH37"	Ubiquitin carboxyl-terminal hydrolase L5	UCHL5	51377	ENSG00000116750			Uchl5 (MGI:1914848)			
chr1	193059421	193091776	1q31	1q31.2		600063	"TROVE2, RO60, SSA2"	"TROVE domain family, member 2"	TROVE2	6738	ENSG00000116747			Trove2 (MGI:106652)			
chr1	193096464	193106534	1q31.2-q31.3	1q31.2		606820	"GLRX2, GRX2"	Glutaredoxin 2	GLRX2	51022	ENSG00000023572			Glrx2 (MGI:1916617)			
chr1	193121957	193254814	1q25-q31	1q31.2		607393	"CDC73, HRPT2, C1orf28"	"Cell division cycle protein 73, S. cerevisiae, homolog of"	CDC73	79577	ENSG00000134371		"Hyperparathyroidism, familial primary, 145000 (3), Autosomal dominant; Hyperparathyroidism-jaw tumor syndrome, 145001 (3), Autosomal dominant; Parathyroid adenoma with cystic changes, 145001 (3), Autosomal dominant; Parathyroid carcinoma, 608266 (3)"	Cdc73 (MGI:2384876)			
chr1	193178729	193186612	1q31	1q31.2		603018	"B3GALT2, GLCT2"	"UDP-galactose:beta-N-acetylglucosamine beta-1,3-galactosyltransferase 2"	B3GALT2	8707	ENSG00000162630			B3galt2 (MGI:1349461)			
chr1	193800000	207100000	1q31.3-q32.1			614826	NYS7	"Nystagmus 7, congenital, autosomal dominant"		101055624		between D1S218 and D1S2655	"Nystagmus 7, congenital, autosomal dominant, 614826 (2), Autosomal dominant"				
chr1	196225778	196608575	1q31.3	1q31.3		610044	"KCNT2, SLICK, EIEE57"	"Potassium channel, subfamily T, member 2"	KCNT2	343450	ENSG00000162687	mutation identified in 1 EIEE57 patient	"?Epileptic encephalopathy, early infantile, 57, 617771 (3), Autosomal dominant"	Kcnt2 (MGI:3036273)			
chr1	196651877	196747503	1q32	1q31.3		134370	"CFH, HF1, HUS, ARMD4, AHUS1"	Complement factor H	CFH	3075	ENSG00000000971		"Basal laminar drusen, 126700 (3), Autosomal dominant; Complement factor H deficiency, 609814 (3), Autosomal recessive, Autosomal dominant; {Hemolytic uremic syndrome, atypical, susceptibility to, 1}, 235400 (3), Autosomal recessive, Autosomal dominant; {Macular degeneration, age-related, 4}, 610698 (3)"	Cfh (MGI:88385)			
chr1	196774799	196794072	1q31-q32.1	1q31.3		605336	"CFHR3, FHR3, HLF4, CFHL3"	Complement factor H-related 3	CFHR3	10878	ENSG00000116785		"{Hemolytic uremic syndrome, atypical, susceptibility to}, 235400 (3), Autosomal recessive, Autosomal dominant; {Macular degeneration, age-related, reduced risk of}, 603075 (3), Autosomal dominant"				
chr1	196819729	196832188	1q31-q32.1	1q31.3		134371	"CFHR1, FHR1, HFL1, CFHL1"	Complement factor H-related 1	CFHR1	3078	ENSG00000244414		"{Hemolytic uremic syndrome, atypical, susceptibility to}, 235400 (3), Autosomal recessive, Autosomal dominant; {Macular degeneration, age-related, reduced risk of}, 603075 (3), Autosomal dominant"	Cfhr1 (MGI:2138169)			
chr1	196888013	196918910	1q31-q32.1	1q31.3		605337	"CFHR4, FHR4, CFHL4"	Complement factor H-related 4	CFHR4	10877	ENSG00000134365						
chr1	196943751	196959327	1q31-q32.1	1q31.3		600889	"CFHR2, FHR2, HFL3, CFHL2"	Complement factor H-related 2	CFHR2	3080	ENSG00000080910	in same 165kb YAC as F13B					
chr1	196975021	197009724	1q32	1q31.3		608593	"CFHR5, CFHL5, FHR5, CFHR5D"	Complement factor H-related 5	CFHR5	81494	ENSG00000134389		"Nephropathy due to CFHR5 deficiency, 614809 (3), Autosomal dominant"				
chr1	197038740	197067266	1q31-q32.1	1q31.3		134580	F13B	"Coagulation factor XIII, B polypeptide"	F13B	2165	ENSG00000143278		"Factor XIIIB deficiency, 613235 (3), Autosomal recessive"	F13b (MGI:88379)			
chr1	197084126	197146693	1q31	1q31.3		605481	"ASPM, MCPH5"	"Abnormal spindle-like, microcephaly-associated"	ASPM	259266	ENSG00000066279		"Microcephaly 5, primary, autosomal recessive, 608716 (3), Autosomal recessive"	Aspm (MGI:1334448)			
chr1	197201461	197478454	1q31-q32.1	1q31.3		604210	"CRB1, RP12, LCA8"	"Crumbs, Drosophila, homolog of, 1"	CRB1	23418	ENSG00000134376		"Leber congenital amaurosis 8, 613835 (3); Pigmented paravenous chorioretinal atrophy, 172870 (3), Autosomal dominant; Retinitis pigmentosa-12, autosomal recessive, 600105 (3), Autosomal recessive"	Crb1 (MGI:2136343)			
chr1	197504747	197782137	1q31.3	1q31.3		613292	"DENND1B, FAM31B, C1orf18"	DENN/MADD domain-containing 1B	DENND1B	163486	ENSG00000213047			Dennd1b (MGI:2447812)			
chr1	197912504	197935475	1q31-q32	1q31.3		606066	LHX9	LIM homeo box gene 9	LHX9	56956	ENSG00000143355			Lhx9 (MGI:1316721)			
chr1	198156977	198322419	1q31.3	1q31.3		606848	NEK7	Never-in-mitosis gene A-related kinase 7	NEK7	140609	ENSG00000151414			Nek7 (MGI:1890645)			
chr1	198638967	198757475	1q31-q32	1q31.3-q32.1		151460	"PTPRC, CD45, LCA"	"Protein tyrosine phosphatase, receptor type, c polypeptide"	PTPRC	5788	ENSG00000081237		"{Hepatitis C virus, susceptibility to}, 609532 (3); Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive, 608971 (3), Autosomal recessive"	Ptprc (MGI:97810)			
chr1	198700000	214400000	1q32			137950	GFND1	Glomerulopathy with fibronectin deposits 1		100689213		max lod at D1S2782	"Glomerulopathy with fibronectin deposits 1, 137950 (2), Autosomal dominant"				
chr1	198700000	236400000	1q32.1-q42			139280	GUK2	Guanylate kinase-2	GUK2	2988		genetic independence of GUK1 and GUK2 unproved					
chr1	198700000	207100000	1q32.1			612381	IBD23	Inflammatory bowel disease 23		100240733		associated with rs3024505	"{Inflammatory bowel disease 23}, 612381 (2)"				
chr1	198700000	214400000	1q32			613164	PARK16	Parkinson disease 16	PARK16	100359403		associated with rs823128	"{Parkinson disease 16}, 613164 (2)"				
chr1	198700000	214400000	1q32			140400	PFHB2	"Progressive familial heart block, type II"		105463127		between D1S70 and D1S505	"Progressive familial heart block, type II, 140400 (2), Autosomal dominant"				
chr1	198858872	198858981	1q31.3	1q32.1		612744	"MIR181B1, MIRN181B1"	Micro RNA 181B1	MIR181B1	406955							
chr1	198859043	198859152	1q31.3	1q32.1		612742	"MIR181A1, MIR213, MIRN181A1"	Micro RNA 181A1	MIR181A1	406995							
chr1	200027601	200177423	1q32.1	1q32.1		604453	"NR5A2, FTF, HB1F"	"Nuclear receptor subfamily 5, group A, member 2 (fetoprotein transcription factor)"	NR5A2	2494	ENSG00000116833			Nr5a2 (MGI:1346834)			
chr1	200551496	200620790	1q31	1q32.1		611279	"KIF14, KIAA0042, MKS12, MCPH20"	Kinesin family member 14	KIF14	9928	ENSG00000118193	mutation identified in 1 MKS12 family	"?Meckel syndrome 12, 616258 (3), Autosomal recessive; Microcephaly 20, primary, autosomal recessive, 617914 (3)"	Kif14 (MGI:1098226)			
chr1	200640806	200669997	1q32.1	1q32.1		615464	"DDX59, OFD5"	DEAD box polypeptide 59	DDX59	83479	ENSG00000118197		"Orofaciodigital syndrome V, 174300 (3), Autosomal recessive"	Ddx59 (MGI:1915247)			
chr1	200738904	200860706	1q32.1	1q32.1		613775	"CAMSAP1L, CAMSAP2, KIAA1078"	Calmodulin-regulated spectrin-associated protein 1-like 1	CAMSAP2	23271	ENSG00000118200			Camsap2 (MGI:1922434)			
chr1	200872954	200874177	1q32.1	1q32.1		602174	GPR25	G protein-coupled receptor-25	GPR25	2848	ENSG00000170128			Gpr25 (MGI:2686146)			
chr1	200969385	201023699	1q31-q32	1q32.1		608322	"KIF21B, KIAA0449"	Kinesin family member 21B	KIF21B	23046	ENSG00000116852			Kif21b (MGI:109234)			
chr1	201039508	201112565	1q32	1q32.1		114208	"CACNA1S, CACNL1A3, CCHL1A3, TTPP1, HOKPP1"	"Calcium channel, voltage-dependent, L type, alpha 1S subunit"	CACNA1S	779	ENSG00000081248	"in mouse, mutation causes muscular dysgenesis"	"Hypokalemic periodic paralysis, type 1, 170400 (3), Autosomal dominant; {Malignant hyperthermia susceptibility 5}, 601887 (3), Autosomal dominant; {Thyrotoxic periodic paralysis, susceptibility to, 1}, 188580 (3), Isolated cases"	Cacna1s (MGI:88294)			
chr1	201134770	201171624	1q41	1q32.1		616877	"TMEM9, TMEM9A, DERM4"	Transmembrane protein 9	TMEM9	252839	ENSG00000116857			Tmem9 (MGI:1913491)			
chr1	201190779	201228951	1q32.1	1q32.1		617309	"IGFN1, EEF1A2BP1"	Immunoglobulin-like and fibronectin type III domains-containing protein 1	IGFN1	91156	ENSG00000163395			Igfn1 (MGI:3045352)			
chr1	201283451	201332992	1q32	1q32.1		601975	PKP1	Plakophilin-1	PKP1	5317	ENSG00000081277		"Ectodermal dysplasia/skin fragility syndrome, 604536 (3)"	Pkp1 (MGI:1328359)			
chr1	201359007	201377827	1q32	1q32.1		191045	"TNNT2, CMH2, CMD1D, RCM3, LVNC6"	"Troponin-T2, cardiac"	TNNT2	7139	ENSG00000118194		"Cardiomyopathy, dilated, 1D, 601494 (3), Autosomal dominant; Cardiomyopathy, familial restrictive, 3, 612422 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 2, 115195 (3), Autosomal dominant; Left ventricular noncompaction 6, 601494 (3), Autosomal dominant"	Tnnt2 (MGI:104597)			
chr1	201380837	201399540	1q25.1-q32.3	1q32.1		602314	LAD1	Ladinin	LAD1	3898	ENSG00000159166			Lad1 (MGI:109343)			
chr1	201403766	201421745	1q31.3	1q32.1		191042	TNNI1	"Troponin-I, skeletal, slow"	TNNI1	7135	ENSG00000159173			Tnni1 (MGI:105073)			
chr1	201464283	201469170	1q31	1q32.1		607054	"PHLDA3, TIH1"	"Pleckstrin homology-like domain, family A, member 3"	PHLDA3	23612	ENSG00000174307			Phlda3 (MGI:1351485)			
chr1	201483529	201507258	1q32	1q32.1		123876	"CSRP1, CSRP"	Cysteine and glycine-rich protein-1	CSRP1	1465	ENSG00000159176			Csrp1 (MGI:88549)			
chr1	201539126	201826973	1q31	1q32.1		611628	"NAV1, POMFIL3, KIAA1151"	Neuron navigator 1	NAV1	89796	ENSG00000134369			Nav1 (MGI:2183683)			
chr1	201808610	201808701	1q32.1	1q32.1		617040	MIR1231	Micro RNA 1231	MIR1231	100302158							
chr1	201888668	201899507	1q32.1	1q32.1		617326	"SHISA4, C1orf40, TMEM58"	"Shisa family, member 4"	SHISA4	149345	ENSG00000198892			Shisa4 (MGI:1924802)			
chr1	201896455	201946587	1q32	1q32.1		602715	"LMOD1, SMLMOD, 1D"	Leiomodin 1	LMOD1	25802	ENSG00000163431			Lmod1 (MGI:2135671)			
chr1	201955490	201970660	1q32	1q32.1		605057	"TIMM17A, TIM17A"	"Translocase of inner mitochondrial membrane 17, yeast, homolog of, A"	TIMM17A	10440	ENSG00000134375			Timm17a (MGI:1343131)			
chr1	201982637	202006146	1q32.1-q32.2	1q32.1		602675	RNPEP	Arginyl aminopeptidase (aminopeptidase B)	RNPEP	6051	ENSG00000176393			Rnpep (MGI:2384902)			
chr1	202010561	202017187	1q32	1q32.1		602191	"ELF3, ESX"	"E74-like factor 3 (ETS domain transcription factor, serine box, epithelial-specific)"	ELF3	1999	ENSG00000163435			Elf3 (MGI:1101781)			
chr1	202118668	202133587	1q32.1	1q32.1		617630	"GPR37L1, ETBRLP2"	G protein-coupled receptor 37-like 1	GPR37L1	9283	ENSG00000170075			Gpr37l1 (MGI:1928503)			
chr1	202133403	202144742	1q32.1	1q32.1		616597	"ARL8A, GIE2"	ADP-ribosylation factor-like 8A	ARL8A	127829	ENSG00000143862			Arl8a (MGI:1915974)			
chr1	202147011	202161587	1q32.1	1q32.1		176889	PTPN7	"Protein tyrosine phosphatase, nonreceptor-type, 7"	PTPN7	5778	ENSG00000143851			Ptpn7 (MGI:2156893)			
chr1	202193989	202319760	1q32	1q32.1		606653	LGR6	Leucine-rich repeat-containing G protein-coupled receptor-6	LGR6	59352	ENSG00000133067			Lgr6 (MGI:2441805)			
chr1	202331656	202341965	1q31	1q32.1		610538	"UBE2T, HSPC150, FANCT"	Ubiquitin-conjugating enzyme E2T	UBE2T	29089	ENSG00000077152		"Fanconi anemia, complementation group T, 616435 (3), Autosomal recessive"	Ube2t (MGI:1914446)			
chr1	202348701	202588568	1q32.1	1q32.1		603768	"PPP1R12B, MYPT2"	"Protein phosphatase 1, regulatory subunit 12B (myosin phosphatase target subunit 2)"	PPP1R12B	4660	ENSG00000077157						
chr1	202590595	202710443	1q32.1	1q32.1		600104	"SYT2, CMS7, MYSPC"	Synaptotagmin-2	SYT2	127833	ENSG00000143858		"Myasthenic syndrome, congenital, 7, presynaptic, 616040 (3), Autosomal dominant"	Syt2 (MGI:99666)			
chr1	202725184	202809469	1q32	1q32.1		605393	"KDM5B, JARID1B, PUT1, PLU1, RBBP2H1A"	Lysine-specific demethylase 5B	KDM5B	10765	ENSG00000117139			Kdm5b (MGI:1922855)			
chr1	202878281	202889256	1q32-q41	1q32.1		603417	"RABIF, RASGFR3, MSS4"	Rab-interacting factor (Ras-specific guanine-releasing factor-3; mammalian suppressor of SEC4)	RABIF	5877	ENSG00000183155			Rabif (MGI:2138605)			
chr1	202891095	202928643	1q32.1	1q32.1		614522	"KLHL12, DKIR"	Kelch-like 12	KLHL12	59349	ENSG00000117153			Klhl12 (MGI:2385619)			
chr1	202940824	202958571	1q32.1	1q32.1		607945	"ADIPOR1, CGI45"	Adiponectin receptor 1	ADIPOR1	51094	ENSG00000159346			Adipor1 (MGI:1919924)			
chr1	202961872	202967275	1q32	1q32.1		608341	"CYB5BR1, NQO3A2, B5R.1"	Cytochrome b5 reductase 1	CYB5R1	51706	ENSG00000159348			Cyb5r1 (MGI:1919267)			
chr1	203026490	203078735	1q32.1	1q32.1		603145	PPFIA4	"Protein-tyrosine phosphatase, receptor-type, F polypeptide-interacting protein alpha 4"	PPFIA4	8497	ENSG00000143847						
chr1	203083128	203086037	1q31-q41	1q32.1		159980	"MYOG, MYF4"	Myogenic factor-4; myogenin	MYOG	4656	ENSG00000122180			Myog (MGI:97276)			
chr1	203127704	203167404	1q32.1	1q32.1		102775	"ADORA1, RDC7"	Adenosine A1 receptor	ADORA1	134	ENSG00000163485			Adora1 (MGI:99401)			
chr1	203167810	203175813	1q32.1	1q32.1		160795	MYBPH	Myosin-binding protein H	MYBPH	4608	ENSG00000133055			Mybph (MGI:1858196)			
chr1	203178930	203186793	1q32.1	1q32.1		601525	"CHI3L1, GP39, YKL40, ASRT7"	Chitinase 3-like 1 (cartilage glycoprotein-39)	CHI3L1	1116	ENSG00000133048		"{Asthma-related traits, susceptibility to, 7}, 611960 (3); {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"	Chil1 (MGI:1340899)			
chr1	203216078	203229731	1q31-q32	1q32.1		600031	"CHIT, CHITD"	Chitotriosidase	CHIT1	1118	ENSG00000133063		"[Chitotriosidase deficiency], 614122 (3), Autosomal recessive"	Chit1 (MGI:1919134)			
chr1	203305535	203309601	1q32	1q32.1		601597	"BTG2, PC3"	B-cell translocation gene 2 (pheochromocytoma cell-3)	BTG2	7832	ENSG00000159388			Btg2 (MGI:108384)			
chr1	203340620	203351428	1q32.1	1q32.1		600245	FMOD	Fibromodulin	FMOD	2331	ENSG00000122176			Fmod (MGI:1328364)			
chr1	203475754	203491351	1q32	1q32.1		601914	PRELP	Proline arginine-rich end leucine-rich repeat protein	PRELP	5549	ENSG00000188783			Prelp (MGI:2151110)			
chr1	203626786	203744080	1q25-q32	1q32.1		108732	"ATP2B4, ATP2B2, PMCA4"	"ATPase, Ca++ transporting, plasma membrane, 4"	ATP2B4	493	ENSG00000058668			Atp2b4 (MGI:88111)			
chr1	203795536	203854127	1q32.1	1q32.1		613513	"ZC3H11A, KIAA0663"	Zinc finger CCCH domain-containing protein 11A	ZC3H11A	9877	ENSG00000257315			Zc3h11a (MGI:1917829)			
chr1	203797522	203801073	1q32.1	1q32.1		613512	ZBED6	Zinc finger BED domain-containing protein 6	ZBED6	100381270	ENSG00000257315	in intron 1 of ZC3H11A		Zbed6 (MGI:3828086)			
chr1	203861584	203871151	1q32	1q32.1		128260	"SNRPE, HYPT11"	Small nuclear ribonucleoprotein polypeptide E	SNRPE	6635	ENSG00000182004		"Hypotrichosis 11, 615059 (3), Autosomal dominant"	Snrpert (MGI:3650419)			
chr1	204073095	204127742	1q32	1q32.1		604748	"SOX13, ICA12"	SRY-box 13	SOX13	9580	ENSG00000143842			Sox13 (MGI:98361)			
chr1	204131060	204152181	1q32.1	1q32.1		609859	"ETNK2, EKI2"	Ethanolamine kinase 2	ETNK2	55224	ENSG00000143845			Etnk2 (MGI:2443760)			
chr1	204154815	204166336	1q32	1q32.1		179820	"REN, HNFJ2"	Renin	REN	5972	ENSG00000143839	~24cM distal to AT3	"[Hyperproreninemia] (3); Hyperuricemic nephropathy, familial juvenile 2, 613092 (3), Autosomal dominant; Renal tubular dysgenesis, 267430 (3), Autosomal recessive"	Ren1 (MGI:97898)			
chr1	204190340	204196490	1q32	1q32.1		603286	"KISS1, HH13"	KISS1 metastasis suppressor	KISS1	3814	ENSG00000170498	mutation identified in 1 HH13 family	"?Hypogonadotropic hypogonadism 13 with or without anosmia, 614842 (3), Autosomal recessive"	Kiss1 (MGI:2663985)			
chr1	204218850	204378376	1q32.1	1q32.1		607771	"PEPP3, KIAA0969"	Phosphatidylinositol 3-phosphate-binding PH domain protein 3	PLEKHA6	22874	ENSG00000143850						
chr1	204398683	204412453	1q32.1	1q32.1		613257	"PPP1R15B, CREP, MSSGM2"	"Protein phosphatase 1, regulatory subunit 15B"	PPP1R15B	84919	ENSG00000158615		"Microcephaly, short stature, and impaired glucose metabolism 2, 616817 (3), Autosomal recessive"	Ppp1r15b (MGI:2444211)			
chr1	204422629	204494814	1q32	1q32.1		602838	PIK3C2B	"Phosphatidylinositol 3-kinase, class 2, beta polypeptide"	PIK3C2B	5287	ENSG00000133056			Pik3c2b (MGI:2685045)			
chr1	204516376	204558119	1q32	1q32.1		602704	MDM4	"Mouse double minute 4, homolog of"	MDM4	4194	ENSG00000198625			Mdm4 (MGI:107934)			
chr1	204617169	204685835	1q32.1	1q32.1		605492	GAC1	Glioma amplification on chromosome 1	LRRN2	10446	ENSG00000170382			Lrrn2 (MGI:106037)			
chr1	204828651	205022821	1q32.1	1q32.1		609145	"NFASC, KIAA0756"	Neurofascin	NFASC	23114	ENSG00000163531			Nfasc (MGI:104753)			
chr1	205042936	205078271	1q32.1	1q32.1		190197	"CNTN2, TAX, TAX1, FAME5"	Contactin 2 (transiently-expressed axonal glycoprotein)	CNTN2	6900	ENSG00000184144	1 family identified with mutation	"?Epilepsy, myoclonic, familial adult, 5, 615400 (3), Autosomal recessive"	Cntn2 (MGI:104518)			
chr1	205086141	205122021	1q32	1q32.1		600697	"RBBP5, RBQ3"	Retinoblastoma-binding protein-5	RBBP5	5929	ENSG00000117222			Rbbp5 (MGI:1918367)			
chr1	205142496	205211598	1q32.1	1q32.1		612666	"DSTYK, KIAA0472, RIP5, DUSTYPK, CAKUT1, SPG23"	Dual serine/threonine and tyrosine protein kinase	DSTYK	25778	ENSG00000133059		"Congenital anomalies of kidney and urinary tract 1, 610805 (3), Autosomal dominant; Spastic paraplegia 23, 270750 (3), Autosomal recessive"	Dstyk (MGI:1925064)			
chr1	205302058	205321790	1q32	1q32.1		608131	"NUAK2, SNARK"	"NUAK family, SNF1-like kinase, 2"	NUAK2	81788	ENSG00000163545			Nuak2 (MGI:1921387)			
chr1	205336063	205357089	1q32.1	1q32.1		614503	KLHDC8A	Kelch domain-containing protein 8A	KLHDC8A	55220	ENSG00000162873			Klhdc8a (MGI:2442630)			
chr1	205381377	205449955	1q32.1	1q32.1		610480	LEMD1	LEM domain-containing protein 1	LEMD1	93273	ENSG00000186007						
chr1	205434885	205456085	1q32.1	1q32.1		615480	"BLACAT1, LINC00912"	"Bladder cancer-associated transcript 1, noncoding"	BLACAT1	101669762							
chr1	205504555	205532792	1q31-q32	1q32.1		169190	"CDK18, PCTK3"	Cyclin-dependent kinase 18	CDK18	5129	ENSG00000117266			Cdk18 (MGI:97518)			
chr1	205607942	205632871	1q32	1q32.1		600246	"ELK4, SAP1"	"ELK4, ETS-domain protein (SRF accessory protein 1)"	ELK4	2005	ENSG00000158711			Elk4 (MGI:102853)			
chr1	205657852	205680501	1q32.1	1q32.1		605097	"SLC45A3, PRST, PCANAP6, IPCA6"	"Solute carrier family 45, member 3 (prostein)"	SLC45A3	85414	ENSG00000158715			Slc45a3 (MGI:1922082)			
chr1	205712818	205750243	1q32.1	1q32.1		611912	"NUCKS1, NUCKS"	Nuclear casein kinase and cyclin-dependent kinase substrate 1	NUCKS1	64710	ENSG00000069275			Nucks1 (MGI:1934811)			
chr1	205767985	205775486	1q32	1q32.1		603949	RAB7L1	RAB7-like 1	RAB29	8934	ENSG00000117280			Rab29 (MGI:2385107)			
chr1	205789092	205813758	1q31-q32	1q32.1		610801	SLC41A1	"Solute carrier family 41, member 1"	SLC41A1	254428	ENSG00000133065			Slc41a1 (MGI:2444823)			
chr1	205813810	205850147	1q32.1	1q32.1		617124	PM20D1	Peptidase M20 domain-containing protein 1	PM20D1	148811	ENSG00000162877			Pm20d1 (MGI:2442939)			
chr1	205913047	205943471	1q32.1	1q32.1		608481	SLC26A9	"Solute carrier family 26 (sulfate transporter), member 9"	SLC26A9	115019	ENSG00000174502			Slc26a9 (MGI:2444594)			
chr1	206009263	206023908	1q31	1q32.1		116890	CTSE	Cathepsin E	CTSE	1510	ENSG00000196188	closely linked to REN		Ctse (MGI:107361)			
chr1	206052722	206102700	1q32.1	1q32.1		616088	"C1orf186, RHEX"	Chromosome 1 open reading frame 186	RHEX	440712	ENSG00000263961						
chr1	206106935	206117049	1q32	1q32.1		600264	"AVPR1B, AVPR3"	Arginine vasopressin receptor-1B	AVPR1B	553	ENSG00000198049			Avpr1b (MGI:1347010)			
chr1	206186178	206205345	1q32	1q32.1		614710	"FAM72A, LMPIP, UGENE"	"Family with sequence similarity 72, member A"	FAM72A	729533	ENSG00000196550			Fam72a (MGI:1919669)			
chr1	206203555	206464442	1q32.1	1q32.1		606524	"SRGAP2, KIAA0456"	"Slit-robo GTPase-activating protein, rho, 2"	SRGAP2	23380	ENSG00000266028			Srgap2 (MGI:109605)			
chr1	206470242	206496889	1q32.1	1q32.1		605048	IKBKE	I-kappa-B kinase-epsilon	IKBKE	9641	ENSG00000263528			Ikbke (MGI:1929612)			
chr1	206507529	206589283	1q32.1	1q32.1		607020	"RASSF5, NORE1"	"Ras association (RalGDS/AF-6) domain family 5 (Nore1, mouse, homolog of)"	RASSF5	83593	ENSG00000266094			Rassf5 (MGI:1926375)			
chr1	206572483	206612550	1q32.1	1q32.1		613709	"EIF2D, HCA56"	Eukaryotic translation initiation factor 2D	EIF2D	1939	ENSG00000143486			Eif2d (MGI:109342)			
chr1	206635535	206655157	1q32.2	1q32.1		603497	DYRK3	Dual-specificity tyrosine phosphorylation-regulated kinase 3	DYRK3	8444	ENSG00000143479			Dyrk3 (MGI:1330300)			
chr1	206684911	206734284	1q32.1	1q32.1		602006	"MAPKAPK2, MK2"	Mitogen-activated protein kinase-activated protein kinase 2	MAPKAPK2	9261	ENSG00000162889			Mapkapk2 (MGI:109298)			
chr1	206767602	206772493	1q31-q32	1q32.1		124092	"IL10, CSIF, GVHDS"	Interleukin-10	IL10	3586	ENSG00000136634		"{Graft-versus-host disease, protection against}, 614395 (3); {HIV-1, susceptibility to}, 609423 (3); {Rheumatoid arthritis, progression of}, 180300 (3)"	Il10 (MGI:96537)			
chr1	206798869	206842980	1q32	1q32.1		605687	IL19	Interleukin 19	IL19	29949	ENSG00000142224			Il19 (MGI:1890472)			
chr1	206865246	206869222	1q32	1q32.1		605619	IL20	Interleukin 20	IL20	50604	ENSG00000162891			Il20 (MGI:1890473)			
chr1	206897403	206904138	1q32	1q32.1		604136	"IL24, ST16, MDA7"	Interleukin 24 (suppression of tumorigenicity 16)	IL24	11009	ENSG00000162892			Il24 (MGI:2135548)			
chr1	206903281	206922032	1q32.2	1q32.1		606015	"FAIM3, TOSO, FCMR"	Fas apoptotic inhibitory molecule 3	FCMR	9214	ENSG00000162894			Fcmr (MGI:1916419)			
chr1	206928521	206946465	1q31-q42	1q32.1		173880	PIGR	Polymeric immunoglobulin receptor	PIGR	5284	ENSG00000162896			Pigr (MGI:103080)			
chr1	206957954	206970656	1q32.3	1q32.1		605484	FCAMR	"Fc fragment of IgA and IgM, receptor for"	FCAMR	83953	ENSG00000162897			Fcamr (MGI:1927803)			
chr1	207018520	207032760	1q32.2	1q32.1		611680	"SARG, C1orf116"	Specifically androgen-regulated gene	C1orf116	79098	ENSG00000182795			AA986860 (MGI:2138143)			
chr1	207043848	207052979	1q32.1	1q32.1		612023	"YOD1, OTUD2, DUBA8"	"YOD1 OTU deubiquitinating enzyme 1, S. cerevisiae, homolog of"	YOD1	55432	ENSG00000180667			Yod1 (MGI:2442596)			
chr1	207053062	207081022	1q31	1q32.1		171835	PFKFB2	"Fructose-2,6-bisphosphatase, cardiac isozyme"	PFKFB2	5208	ENSG00000123836			Pfkfb2 (MGI:107815)			
chr1	207088794	207099992	1q32	1q32.1		120831	C4BPB	"Complement component 4-binding protein, beta polypeptide"	C4BPB	725	ENSG00000123843						
chr1	207104231	207144971	1q32	1q32.2		120830	C4BPA	"Complement component 4-binding protein, alpha polypeptide"	C4BPA	722	ENSG00000123838	same RE fragment as C4BPB					
chr1	207321471	207360965	1q32	1q32.2		125240	"CD55, DAF, CROM, CHAPLE"	CD55 antigen (blood group Cromer)	CD55	1604	ENSG00000196352		"[Blood group Cromer], 613793 (3), Autosomal recessive; Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy, 226300 (3), Autosomal recessive"	"Cd55,Cd55b (MGI:104850,MGI:104849)"			
chr1	207454299	207489894	1q32	1q32.2		120650	"CR2, C3DR, SLEB9, CVID7"	Complement component (3d/Epstein-Barr virus) receptor-2	CR2	1380	ENSG00000117322		"Immunodeficiency, common variable, 7, 614699 (3), Autosomal recessive; {Systemic lupus erythematosus, susceptibility to, 9}, 610927 (3)"	Cr2 (MGI:88489)			
chr1	207496127	207641764	1q32	1q32.2		120620	"CR1, C3BR"	Complement component (3b/4b) receptor-1	CR1	1378	ENSG00000203710		"[Blood group, Knops system], 607486 (3); CR1 deficiency (1); {Malaria, severe, resistance to}, 611162 (3); {?SLE susceptibility} (1)"				
chr1	207645112	207723690	1q32	1q32.2		605886	CR1L	Complement component receptor 1-like	CR1L	1379	ENSG00000197721			Cr1l (MGI:88513)			
chr1	207752037	207795515	1q32	1q32.2		120920	"MCP, CD46, AHUS2"	"Membrane cofactor protein (CD46, trophoblast-lymphocyte cross-reactive antigen)"	CD46	4179	ENSG00000117335		"{Hemolytic uremic syndrome, atypical, susceptibility to, 2}, 612922 (3), Autosomal recessive, Autosomal dominant"	Cd46 (MGI:1203290)			
chr1	207801851	207801938	1q32.2	1q32.2		610784	"MIR29C, MIRN29C"	Micro RNA 29C	MIR29C	407026							
chr1	207886537	207911337	1q32	1q32.2		142230	CD34	CD34 antigen	CD34	947	ENSG00000174059			Cd34 (MGI:88329)			
chr1	208022241	208244319	1q32.2	1q32.2		601054	"PLXNA2, OCT, PLXN2"	Plexin A2 (OCT transmembrane protein)	PLXNA2	5362	ENSG00000076356			Plxna2 (MGI:107684)			
chr1	209432132	209432241	1q32.2	1q32.2		613147	"MIR205, MIRN205"	Micro RNA 205	MIR205	406988							
chr1	209583699	209613938	1q32-q41	1q32.2		614994	"CAMK1G, CLICK3"	Calcium/calmodulin-dependent protein kinase IG	CAMK1G	57172	ENSG00000008118			Camk1g (MGI:2388073)			
chr1	209614869	209652474	1q32	1q32.2		150310	"LAMB3, AI1A"	"Laminin, beta-3 (nicein, 125kD; kalinin, 140kD; BM600, 125kD)"	LAMB3	3914	ENSG00000196878		"Amelogenesis imperfecta, type IA, 104530 (3), Autosomal dominant; Epidermolysis bullosa, junctional, Herlitz type, 226700 (3), Autosomal recessive; Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3), Autosomal recessive"	Lamb3 (MGI:99915)			
chr1	209675324	209676389	1q32-q41	1q32.2		614447	G0S2	G0/G1 switch gene 2	G0S2	50486	ENSG00000123689			G0s2 (MGI:1316737)			
chr1	209686179	209734949	1q32-q41	1q32.2		600713	"HSD11B1, HSD11, HSD11L, CORTRD2"	"Hydroxysteroid, 11-beta, dehydrogenase 1"	HSD11B1	3290	ENSG00000117594	digenic triallelic mutations with H6PD	"Cortisone reductase deficiency 2, 614662 (3), Autosomal dominant"	Hsd11b1 (MGI:103562)			
chr1	209756031	209782322	1q32.3-q41	1q32.2		608255	"TRAF3IP3, T3JAM"	TRAF3-interacting protein 3	TRAF3IP3	80342	ENSG00000009790			Traf3ip3 (MGI:2441706)			
chr1	209785622	209806174	1q32-q41	1q32.2		607199	"IRF6, VWS, LPS, PIT, PPS1, OFC6"	Interferon regulatory factor 6	IRF6	3664	ENSG00000117595	OFC6 in enhancer 5' of IRF6	"{Orofacial cleft 6}, 608864 (3), Isolated cases; Popliteal pterygium syndrome 1, 119500 (3), Autosomal dominant; van der Woude syndrome, 119300 (3), Autosomal dominant"	Irf6 (MGI:1859211)			
chr1	209938164	210171314	1q32.2	1q32.2		610949	"SYT14, SCAR11"	Synaptotagmin 14	SYT14	255928	ENSG00000143469		"Spinocerebellar ataxia, autosomal recessive 11, 614229 (3), Autosomal recessive"	Syt14 (MGI:2444490)			
chr1	210327872	210676297	1q32	1q32.2		605743	"HHAT, MART2, SKI1"	Hedgehog acyltransferase	HHAT	55733	ENSG00000054392			Hhat (MGI:2444681)			
chr1	210678313	211134114	1q32-q41	1q32.2		603305	"KCNH1, EAG, TMBTS, ZLS1"	"Potassium voltage-gated channel, subfamily H, member 1 (ether-a-go-go, drosophila, homolog of)"	KCNH1	3756	ENSG00000143473		"Temple-Baraitser syndrome, 611816 (3), Autosomal dominant; Zimmermann-Laband syndrome 1, 135500 (3), Autosomal dominant"	Kcnh1 (MGI:1341721)			
chr1	211326593	211374945	1q32	1q32.3		602356	TRAF5	TNF receptor-associated factor 5	TRAF5	7188	ENSG00000082512			Traf5 (MGI:107548)			
chr1	211476521	211492916	1q32.3	1q32.3		180040	"RD3, LCA12, C1orf36"	"Retinal degeneration 3, mouse, homolog of"	RD3	343035	ENSG00000198570		"Leber congenital amaurosis 12, 610612 (3), Autosomal recessive"	Rd3 (MGI:1921273)			
chr1	211575038	211578756	1q32.3	1q32.3		609521	"SLC30A1, ZNT1"	"Solute carrier family 30 (zinc transporter), member 1"	SLC30A1	7779	ENSG00000170385			Slc30a1 (MGI:1345281)			
chr1	211658255	211675629	1q32.2-q41	1q32.3		604043	"NEK2, RP67"	Never in mitosis gene a-related kinase 2	NEK2	4751	ENSG00000117650	"pseudogenes on chr. 2, 14, and 22; mutation identified in 1 family"	"?Retinitis pigmentosa 67, 615565 (3), Autosomal recessive"	Nek2 (MGI:109359)			
chr1	211940327	212035659	1q32.3	1q32.3		611350	"INTS7, INT7"	Integrator complex subunit 7	INTS7	25896	ENSG00000143493			Ints7 (MGI:1924315)			
chr1	212035552	212105005	1q32.1-q32.2	1q32.3		610617	"DTL, RAMP, DCAF2, CDT2"	"Denticleless, Drosophila, homolog of"	DTL	51514	ENSG00000143476			Dtl (MGI:1924093)			
chr1	212285536	212361862	1q41	1q32.3		601643	PPP2R5A	"Protein phosphatase-2, regulatory subunit B (B56), alpha isoform"	PPP2R5A	5525	ENSG00000066027			Ppp2r5a (MGI:2388479)			
chr1	212432886	212446378	1q32.3	1q32.3		611874	"NENF, CIR2"	Neuron-derived neurotrophic factor	NENF	29937	ENSG00000117691			Nenf (MGI:1913458)			
chr1	212565333	212620776	1q32.3	1q32.3		603148	ATF3	Activating transcription factor 3	ATF3	467	ENSG00000162772			Atf3 (MGI:109384)			
chr1	212686416	212699984	1p32.3	1q32.3		612470	BATF3	"Basic leucine zipper transcription factor, ATF-like, 3"	BATF3	55509	ENSG00000123685			Batf3 (MGI:1925491)			
chr1	212726152	212798899	1q41	1q32.3		609174	"NSL1, DC8, C1orf48"	"NSL1, MIS12 kinetochore complex component"	NSL1	25936	ENSG00000117697			Nsl1 (MGI:2685830)			
chr1	212856603	212858137	1q31	1q32.3		610864	LQK1	LQK1 protein	FLVCR1-DT	642946							
chr1	212858254	212899362	1q31.3	1q32.3		609144	"FLVCR1, AXPC1, PCARP"	Feline leukemia virus subgroup C receptor 1	FLVCR1	28982	ENSG00000162769		"Ataxia, posterior column, with retinitis pigmentosa, 609033 (3), Autosomal recessive"	Flvcr1 (MGI:2444881)			
chr1	212935542	212992304	1q32.3	1q32.3		610471	VASH2	Vasohibin 2	VASH2	79805	ENSG00000143494			Vash2 (MGI:2444826)			
chr1	213051232	213378752	1q32.3	1q32.3		617517	"RPS6KC1, RPK118"	Ribosomal protein S6 kinase C1	RPS6KC1	26750	ENSG00000136643			Rps6kc1 (MGI:2443419)			
chr1	213924748	213926653	1q41	1q32.3		614635	"LINC00538, YIYA"	Long intergenic noncoding RNA 538	LINC00538	100861504							
chr1	213983238	214041509	1q32.2-q32.3	1q32.3		601546	PROX1	Prospero-related homeo box 1	PROX1	5629	ENSG00000117707			Prox1 (MGI:97772)			
chr1	214281221	214337135	1q41	1q32.3		610663	SMYD2	SET and MYND domain-containing protein 2	SMYD2	56950	ENSG00000143499			Smyd2 (MGI:1915889)			
chr1	214348695	214551680	1q32	1q32-q41		603155	"PTPN14, PEZ, CATLPH"	"Protein tyrosine phosphatase, nonreceptor-type, 14"	PTPN14	5784	ENSG00000152104	mutation identified in 1 CATLPH family	"?Choanal atresia and lymphedema, 613611 (3), Autosomal recessive"	Ptpn14 (MGI:102467)			
chr1	214400000	236400000	1q41-q42			610836	AUTS11	"Autism, susceptibility to, 11"		100188820		"associated with rs12740310, rs3737296, and rs12310279"	"{Autism susceptibility 11}, 610836 (2)"				
chr1	214400000	236400000	1q41-q42			612530	"DEL1q41q42, C1DELq41q42"	Chromosome 1q41-q42 deletion syndrome				contiguous gene deletion of 1.7Mb	"Chromosome 1q41-q42 deletion syndrome, 612530 (4), Isolated cases"				
chr1	214400000	248956422	1q41-q44			615589	OTSC10	Otosclerosis 10	OTSC10	102723100			"Otosclerosis 10, 615589 (2), Autosomal dominant"				
chr1	214400000	223900000	1q41			600332	RMD1	Rippling muscle disease 1	RMD1	6022			"Rippling muscle disease-1, 600332 (2), Autosomal dominant"				
chr1	214603188	214664570	1q32-q41	1q41		600236	"CENPF, CILD31, STROMS"	"Centromere autoantigen F, 400kD"	CENPF	1063	ENSG00000117724		"Stromme syndrome, 243605 (3), Autosomal recessive"	Cenpf (MGI:1313302)			
chr1	215002919	215237092	1q41	1q41		603219	"KCNK2, TREK"	"Potassium channel, subfamily K, member 2"	KCNK2	3776	ENSG00000082482			Kcnk2 (MGI:109366)			
chr1	215567378	215621820	1q41	1q41		613272	KCTD3	Potassium channel tetramerization domain-containing protein 3	KCTD3	51133	ENSG00000136636			Kctd3 (MGI:2444629)			
chr1	215622893	216423395	1q41	1q41		608400	"USH2A, RP39"	Usherin	USH2A	7399	ENSG00000042781		"Retinitis pigmentosa 39, 613809 (3); Usher syndrome, type 2A, 276901 (3), Autosomal recessive"	Ush2a (MGI:1341292)			
chr1	216503245	217137754	1q41	1q41		602969	ESRRG	"Estrogen-related receptor, gamma"	ESRRG	2104	ENSG00000196482			Esrrg (MGI:1347056)			
chr1	217426991	217631111	1q41	1q41		616836	"GPATCH2, GPATC2"	G-patch domain-containing protein 2	GPATCH2	55105	ENSG00000092978			Gpatch2 (MGI:1915019)			
chr1	217631323	217868150	1q41	1q41		611032	"SPATA17, MSRG11"	Spermatogenesis-associated protein 17	SPATA17	128153	ENSG00000162814			Spata17 (MGI:1921967)			
chr1	218285286	218337982	1q41	1q41		611193	RRP15	"Ribosomal RNA-processing 15, S. cerevisiae, homolog of"	RRP15	51018	ENSG00000067533			Rrp15 (MGI:1914473)			
chr1	218345283	218444618	1q41	1q41		190220	"TGFB2, LDS4"	"Transforming growth factor, beta-2"	TGFB2	7042	ENSG00000092969		"Loeys-Dietz syndrome 4, 614816 (3), Autosomal dominant"	Tgfb2 (MGI:98726)			
chr1	219173830	219445120	1q41	1q41		616548	LYPLAL1	Lysophospholipase-like 1	LYPLAL1	127018	ENSG00000143353			Lyplal1 (MGI:2385115)			
chr1	219910394	219960103	1q41	1q41		611146	"SLC30A10, ZNT10, HMNDYT1"	"Solute carrier family 30 (zinc transporter), member 10"	SLC30A10	55532	ENSG00000196660		"Hypermanganesemia with dystonia 1, 613280 (3), Autosomal recessive"	Slc30a10 (MGI:2685058)			
chr1	219968599	220046657	1q41-q42	1q41		138295	"EPRS, PARS"	Glutamyl-prolyl-tRNA synthetase	EPRS	2058	ENSG00000136628			Eprs (MGI:97838)			
chr1	220057481	220089915	1q41	1q41		604053	BPNT1	"3'(2'),5'-bisphosphate nucleotidase 1"	BPNT1	10380	ENSG00000162813			Bpnt1 (MGI:1338800)			
chr1	220094112	220148040	1q41	1q41		612801	"IARS2, CAGSSS"	Isoleucyl-tRNA synthetase 2	IARS2	55699	ENSG00000067704	mutation identified in 1 CAGSSS family	"?Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia, 616007 (3), Autosomal recessive"	Iars2 (MGI:1919586)			
chr1	220117852	220117961	1q41	1q41		610943	"MIR215, MIRN215"	Micro RNA 215	MIR215	406997							
chr1	220118156	220118240	1q41	1q41		610940	"MIR194-1, MIRN194-1"	Micro RNA 194-1	MIR194-1	406969							
chr1	220148267	220272500	1q41	1q41		609275	"RAB3GAP2, RAB3GAP150, p150, KIAA0839, WARBM2"	RAB3 GTPase-activating protein (noncatalytic) subunit 2	RAB3GAP2	25782	ENSG00000118873		"Martsolf syndrome, 212720 (3), Autosomal recessive; Warburg micro syndrome 2, 614225 (3), Autosomal recessive"	Rab3gap2 (MGI:1916043)			
chr1	220528182	220664456	1q41	1q41		606511	"MARK1, KIAA1477"	MAP/microtubule affinity-regulating kinase 1	MARK1	4139	ENSG00000116141			Mark1 (MGI:2664902)			
chr1	220747416	220784814	1q41	1q41		614127	"MOSC2, MARC2"	Molybdenum cofactor sulfurase C-terminal domain-containing protein 2	2-Mar	54996	ENSG00000117791			Marc2 (MGI:1914497)			
chr1	220786696	220814398	1q41	1q41		614126	"MOSC1, MARC1"	Molybdenum cofactor sulfurase C-terminal domain-containing protein 1	1-Mar	64757	ENSG00000186205			Marc1 (MGI:1913362)			
chr1	220879400	220885058	1q41-q42.1	1q41		142995	HLX1	H.20-like homeobox 1	HLX	3142	ENSG00000136630			Hlx (MGI:96109)			
chr1	221701419	221742175	1q41	1q41		608867	"DUSP10, MKP5"	Dual-specificity phosphatase 10	DUSP10	11221	ENSG00000143507			Dusp10 (MGI:1927070)			
chr1	222557901	222590095	1q42	1q41		604903	"TAF1A, RAFI48, SL1"	TATA box-binding protein-associated factor 1A	TAF1A	9015	ENSG00000143498			Taf1a (MGI:109578)			
chr1	222618101	222668011	1q42	1q41		613455	"MIA3, TANGO1, TANGO, KIAA0268"	"Melanoma inhibitory activity family, member 3"	MIA3	375056	ENSG00000154305			Mia3 (MGI:2443183)			
chr1	222668012	222712894	1q41	1q41		612375	AIDA	"Axin interactor, dorsalization-associated"	AIDA	64853	ENSG00000186063			Aida (MGI:1919737)			
chr1	222814513	223005994	1q42	1q41		607502	DISPA	"Dispatched, Drosophila, homolog of, A"	DISP1	84976	ENSG00000154309			Disp1 (MGI:1916147)			
chr1	223108400	223143281	1q41	1q41		603031	"TLR5, TIL3, SLEB1, MELIOS"	Toll-like receptor-5	TLR5	7100	ENSG00000187554		"{Legionnaire disease, susceptibility to}, 608556 (3); {Melioidosis, susceptibility to}, 615557 (3); {Systemic lupus erythematosus, resistance to}, 601744 (3); {Systemic lupus erythematosus, susceptibility to, 1}, 601744 (3)"	Tlr5 (MGI:1858171)			
chr1	223220818	223365270	1q41	1q41		615827	SUSD4	Sushi domain-containing protein 4	SUSD4	55061	ENSG00000143502			Susd4 (MGI:2138351)			
chr1	223701592	223776017	1q41-q42	1q41		114230	CAPN2	"Calpain, large polypeptide L2"	CAPN2	824	ENSG00000162909			Capn2 (MGI:88264)			
chr1	223779892	223845971	1q42.1	1q41		602143	"TP53BP2, ASPP2"	Tumor protein p53-binding protein-2	TP53BP2	7159	ENSG00000143514			Trp53bp2 (MGI:2138319)			
chr1	223900000	236400000	1q42			613058	BCC2	"Basal cell carcinoma, susceptibility to, 2"		100307119		associated with rs801114	"{Basal cell carcinoma, susceptibility to, 2}, 613058 (2)"				
chr1	223900000	236400000	1q42			606554	EA3	"Episodic ataxia, type 3"		780905		max lod at D1S235	"Episodic ataxia, type 3, 606554 (2), Autosomal dominant"				
chr1	223900000	236400000	1q42			143025	HRES1	HTLV-1 related endogenous sequence	HRES1	3272							
chr1	223900000	236400000	1q42			604801	MDC1B	"Muscular dystrophy, congenital, 1B"		53368			"Muscular dystrophy, congenital, 1B, 604801 (2), Autosomal recessive"				
chr1	223900000	236400000	1q42			170000	PEPC	Peptidase C	PEPC	5183		"1q25, 1q32 = conflicting localizations"					
chr1	223900000	230500000	1q42.11-q42.13			180420	RN5S1@	"RNA, 5S cluster 1"	RN5S1@	6025		25-30% at 1q31 (RN5S3@)					
chr1	224114086	224162046	1q42.12	1q42.11		609100	"FBXO28, FBX28, KIAA0483"	F-box only protein 28	FBXO28	23219	ENSG00000143756			Fbxo28 (MGI:1261890)			
chr1	224183207	224193440	1q42.11	1q42.11		615843	"DEGS1, DES1, MLD"	"Delta(4)-desaturase, sphingolipid, 1"	DEGS1	8560	ENSG00000143753			Degs1 (MGI:1097711)			
chr1	224227333	224330188	1q41-q42.2	1q42.11		602426	NVL	Nuclear valosin-containing protein-like	NVL	4931	ENSG00000143748			Nvl (MGI:1914709)			
chr1	224356810	224379451	1q42.11	1q42.11		617483	"CNIH4, CNIH2"	Cornichon family AMPA receptor auxiliary protein 4	CNIH4	29097	ENSG00000143771			Cnih4 (MGI:1925828)			
chr1	224385142	224434766	1q42.13	1q42.11-q42.12		617424	"WDR26, SKDEAS"	WD repeat-containing protein 26	WDR26	80232	ENSG00000162923		"Skraban-Deardorff syndrome, 617616 (3), Autosomal dominant"	Wdr26 (MGI:1923825)			
chr1	224928421	225399293	1q42	1q42.12		603341	"DNAH14, HL18"	"Dynein, axonemal, heavy chain 14"	DNAH14	127602	ENSG00000185842			Dnah14 (MGI:2444525)			
chr1	225401501	225428854	1q42.1	1q42.12		600024	"LBR, PHA"	Lamin B receptor	LBR	3930	ENSG00000143815		"Greenberg skeletal dysplasia, 215140 (3), Autosomal recessive; Pelger-Huet anomaly, 169400 (3), Autosomal dominant; ?Reynolds syndrome, 613471 (3), Autosomal dominant"	Lbr (MGI:2138281)			
chr1	225486828	225660045	1q42.13	1q42.12		609061	"ENAH, ENA, MENA, NDPP1"	"Enabled, Drosophila, homolog of"	ENAH	55740	ENSG00000154380			Enah (MGI:108360)			
chr1	225777812	225790465	1q42.12	1q42.12		600707	"SRP9, ALURBP"	"Signal recognition particle, 9-kD"	SRP9	6726	ENSG00000143742			Srp9 (MGI:1350930)			
chr1	225810073	225845562	1q42.1	1q42.12		132810	EPHX1	"Epoxide hydroxylase 1, microsomal xenobiotic"	EPHX1	2052	ENSG00000143819		"Hypercholanemia, familial, 607748 (3)"	Ephx1 (MGI:95405)			
chr1	225886281	225889145	1q42.1	1q42.12		603037	"LEFTB, LEFTY1"	"Left-right determination, factor B"	LEFTY1	10637	ENSG00000243709			Lefty1 (MGI:107405)			
chr1	225919876	225924339	1q42.13	1q42.12		616406	"PYCR2, HLD10"	Pyrroline-5-carboxylate reductase 2	PYCR2	29920	ENSG00000143811		"Leukodystrophy, hypomyelinating, 10, 616420 (3), Autosomal recessive"	Pycr2 (MGI:1277956)			
chr1	225936597	225941491	1q42.1	1q42.12		601877	"EBAF, TGFB4, LEFTY2, LEFTA, LEFTYA"	"Transforming growth factor, beta-4 (endometrial bleeding-associated factor)"	LEFTY2	7044	ENSG00000143768		Left-right axis malformations (3)	Lefty2 (MGI:2443573)			
chr1	226062706	226072001	1q41	1q42.12		601128	"H3F3A, H3F3"	"H3 histone, family 3A"	H3F3A	3020	ENSG00000163041			"H3f3b,H3f3a (MGI:1101768,MGI:1097686)"			
chr1	226144678	226186721	1q42.1	1q42.12		606809	"ACBD3, GOCAP1, GOLPH1, GCP60"	Acyl-Coenzyme A binding domain containing 3	ACBD3	64746	ENSG00000182827			Acbd3 (MGI:2181074)			
chr1	226223617	226227054	1q42.1	1q42.12		609852	"MIXL1, MIXL, MIX"	MIX1 homeobox-like protein 1	MIXL1	83881	ENSG00000185155			Mixl1 (MGI:1351322)			
chr1	226231148	226310081	1q42.12	1q42.12		609375	LIN9	"Lin9, C. elegans, homolog of"	LIN9	286826	ENSG00000183814			Lin9 (MGI:1919818)			
chr1	226360690	226408099	1q42	1q42.12		173870	"PARP1, ADPRT, PPOL, PARP"	Poly(ADP-ribose) polymerase 1	PARP1	142	ENSG00000143799	?processed pseudogenes on chr.13 and 14		Parp1 (MGI:1340806)			
chr1	226631689	226739295	1q41-q43	1q42.12		147522	ITPKB	"Inositol 1,4,5-trisphosphate 3-kinase B"	ITPKB	3707	ENSG00000143772			Itpkb (MGI:109235)			
chr1	226870571	226903828	1q31-q42	1q42.13		600759	"PSEN2, AD4, STM2, CMD1V"	Presenilin 2	PSEN2	5664	ENSG00000143801		"Alzheimer disease-4, 606889 (3), Autosomal dominant; Cardiomyopathy, dilated, 1V, 613697 (3), Autosomal dominant"	Psen2 (MGI:109284)			
chr1	226939338	226987544	1q42.2	1q42.13		606980	"ADCK3, COQ8, CABC1, SCAR9, ARCA2, COQ10D4"	AARF domain-containing kinase 3	COQ8A	56997	ENSG00000163050		"Coenzyme Q10 deficiency, primary, 4, 612016 (3), Autosomal recessive"	Coq8a (MGI:1914676)			
chr1	226989864	227318501	1q41-q42	1q42.13		603412	"CDC42BPA, PK428, MRCKA"	CDC42-binding protein kinase alpha	CDC42BPA	8476	ENSG00000143776			Cdc42bpa (MGI:2441841)			
chr1	227918655	227947929	1q42	1q42.13		602863	WNT14	"Wingless-type MMTV integration site family, member 14"	WNT9A	7483	ENSG00000143816			Wnt9a (MGI:2446084)			
chr1	228007021	228067112	1q42	1q42.13		606359	WNT3A	"Wingless-type MMTV integration site family, member 3A"	WNT3A	89780	ENSG00000154342			Wnt3a (MGI:98956)			
chr1	228082659	228099211	1q42	1q42.13		103180	ARF1	ADP-ribosylation factor-1	ARF1	375	ENSG00000143761			Arf1 (MGI:99431)			
chr1	228106678	228111745	1q42.13	1q42.13		611859	MRPL55	Mitochondrial ribosomal protein L55	MRPL55	128308	ENSG00000162910			Mrpl55 (MGI:1914462)			
chr1	228140083	228148954	1q32.1-q42	1q42.13		139270	GUK1	Guanylate kinase-1	GUK1	2987	ENSG00000143774			Guk1 (MGI:95871)			
chr1	228149713	228159825	1q42.13	1q42.13		608803	"GJC2, GJA12, CX47, PMLDAR, HLD2, SPG44, LMPH1C"	"Gap junction protein, gamma-2 (47kD)"	GJC2	57165	ENSG00000198835		"Leukodystrophy, hypomyelinating, 2, 608804 (3), Autosomal recessive; Lymphedema, hereditary, IC, 613480 (3), Autosomal dominant; Spastic paraplegia 44, autosomal recessive, 613206 (3), Autosomal recessive"	Gjc2 (MGI:2153060)			
chr1	228165807	228182256	1q42.13	1q42.13		615316	"IBA57, C1orf69, MMDS3, SPG74"	"IBA57, S. cerevisiae, homolog of"	IBA57	200205	ENSG00000181873	mutation identified in 1 MMDS3 family and 1 SPG74 family	"?Multiple mitochondrial dysfunctions syndrome 3, 615330 (3), Autosomal recessive; ?Spastic paraplegia 74, autosomal recessive, 616451 (3), Autosomal recessive"	Iba57 (MGI:3041174)			
chr1	228393671	228406815	1q42.13	1q42.13		607868	TRIM11	Tripartite motif-containing protein 11	TRIM11	81559	ENSG00000154370			Trim11 (MGI:2137355)			
chr1	228406876	228416881	1q42	1q42.13		606123	RNF16	RING finger protein-16	TRIM17	51127	ENSG00000162931			Trim17 (MGI:1861440)			
chr1	228424844	228425324	1q42	1q42.13		602820	"HIST3H3, H3FT, H3T"	"Histone 3, H3"	HIST3H3	8290	ENSG00000168148						
chr1	228457363	228457858	1q42	1q42.13		615015	HIST3H2A	"Histone gene cluster 3, H2A histone"	HIST3H2A	92815	ENSG00000181218			Hist3h2a (MGI:2448458)			
chr1	228458106	228458557	1q42	1q42.13		615046	"HIST3H2BB, H2Bb"	"Histone gene cluster 3, H2B histone family, member B"	HIST3H2BB	128312	ENSG00000196890			Hist3h2bb-ps (MGI:1922442)			
chr1	228487366	228496187	1q42.13	1q42.13		613754	"RNF186, RACO1"	Ring finger protein 187	RNF187	149603	ENSG00000168159			Rnf187 (MGI:1914224)			
chr1	228644646	228746668	1q42	1q42.13		606366	"RHOU, WRCH1"	"Ras homolog gene family, member U"	RHOU	58480	ENSG00000116574			Rhou (MGI:1916831)			
chr1	229271061	229305893	1q42-q43	1q42.13		179511	"RAB4A, RAB4"	Ras-associated protein RAB4A	RAB4A	5867	ENSG00000168118			Rab4a (MGI:105069)			
chr1	229321004	229343794	1q42.13	1q42.13		616762	"CCSAP, CSAP, C1orf96"	"Centriole-, cilia-, and spindle-associated protein"	CCSAP	126731	ENSG00000154429			Ccsap (MGI:1920670)			
chr1	229431244	229434095	1q42.1	1q42.13		102610	"ACTA1, ASMA, NEM3, CFTD1, SHPM"	"Actin, alpha-1, skeletal muscle"	ACTA1	58	ENSG00000143632	mutation identified in 1 SHPM family	"Myopathy, actin, congenital, with cores, 161800 (3), Autosomal recessive, Autosomal dominant; Myopathy, actin, congenital, with excess of thin myofilaments, 161800 (3), Autosomal recessive, Autosomal dominant; Myopathy, congenital, with fiber-type disproportion 1, 255310 (3), Autosomal recessive, Autosomal dominant; ?Myopathy, scapulohumeroperoneal, 616852 (3), Autosomal dominant; Nemaline myopathy 3, autosomal dominant or recessive, 161800 (3), Autosomal recessive, Autosomal dominant"	Acta1 (MGI:87902)			
chr1	229441290	229508341	1q42.13	1q42.13		607613	NUP133	"Nucleoporin, 133kD"	NUP133	55746	ENSG00000069248			Nup133 (MGI:2442620)			
chr1	229516581	229558987	1q42	1q42.13		605454	"ABCB10, MTABC2"	"ATP-binding cassette, subfamily B, member 10"	ABCB10	23456	ENSG00000135776	pseudogene on 15q13-q14		Abcb10 (MGI:1860508)			
chr1	230057788	230282129	1q41-q42	1q42.13		602274	GALNT2	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2	GALNT2	2590	ENSG00000143641			Galnt2 (MGI:894694)			
chr1	230321645	230425927	1q42.13	1q42.13		616791	PGBD5	Piggybac transposable element-derived 5	PGBD5	79605	ENSG00000177614			Pgbd5 (MGI:2429955)			
chr1	230500000	243500000	1q42.2-q43			602759	PCAP	Predisposing for prostate cancer	PCAP	7834			"{Prostate cancer, susceptibility to}, 176807 (2), Autosomal dominant"				
chr1	230500000	243500000	1q42.2-q43			119100	"SHFL1, SHFLD"	Split-hand/foot malformation with long bone deficiency 1		791121		between rs1124110 and rs535043	"Split-hand/foot malformation with long bone deficiency 1, 119100 (2), Autosomal dominant"				
chr1	230642455	230693984	1q42.2	1q42.2		606974	"COG2, LDLC, CDG2Q"	Component of oligomeric golgi complex 2	COG2	22796	ENSG00000135775	mutation identified in 1 CDG2Q patient	"?Congenital disorder of glycosylation, type IIq, 617395 (3), Autosomal recessive"	Cog2 (MGI:1923582)			
chr1	230702522	230714589	1q42-q43	1q42.2		106150	"AGT, SERPINA8"	Angiotensinogen	AGT	183	ENSG00000135744		"{Hypertension, essential, susceptibility to}, 145500 (3), Multifactorial; {Preeclampsia, susceptibility to} (3); Renal tubular dysgenesis, 267430 (3), Autosomal recessive"	Agt (MGI:87963)			
chr1	230747288	230803355	1q42	1q42.2		606401	CAPN9	Calpain 9	CAPN9	10753	ENSG00000135773			Capn9 (MGI:1920897)			
chr1	230979048	231000732	1q42.2	1q42.2		611647	"ARV1, EIEE38"	"ARV1, S. cerevisiae, homolog of"	ARV1	64801	ENSG00000173409		"Epileptic encephalopathy, early infantile, 38, 617020 (3), Autosomal recessive"	Arv1 (MGI:1916115)			
chr1	231162390	231221567	1q42	1q42.2		610584	TRIM67	Tripartite motif-containing protein 67	TRIM67	440730	ENSG00000119283			Trim67 (MGI:3045323)			
chr1	231241172	231277972	1q42	1q42.2		602744	"GNPAT, DHAPAT, RCDP2"	Glyceronephosphate O-acyltransferase	GNPAT	8443	ENSG00000116906		"Rhizomelic chondrodysplasia punctata, type 2, 222765 (3), Autosomal recessive"	Gnpat (MGI:1343460)			
chr1	231332730	231337871	1q42.2	1q42.2		615283	"EXOC8, EXO84, SEC84"	Exocyst complex component 8	EXOC8	149371	ENSG00000116903			Exoc8 (MGI:2142527)			
chr1	231337935	231355028	1q42.2	1q42.2		616086	"SPRTN, DVC1, C1orf124, RJALS"	SprT-like N-terminal domain protein	SPRTN	83932	ENSG00000010072		"Ruijs-Aalfs syndrome, 616200 (3), Autosomal recessive"	Sprtn (MGI:2685351)			
chr1	231363750	231425043	1q42-q43	1q42.2		606425	"EGLN1, PHD2, HIFPH2, C1orf12, ZMYND6, SM20, ECYT3, HALAH"	"Egl9, C. elegans, homolog of, 1"	EGLN1	54583	ENSG00000135766		"Erythrocytosis, familial, 3, 609820 (3), Autosomal dominant; [Hemoglobin, high altitude adaptation], 609070 (3), Autosomal dominant"	Egln1 (MGI:1932286)			
chr1	231528652	231566523	1q41	1q42.2		602964	"TSNAX, TRAX"	Translin-associated factor X	TSNAX	7257	ENSG00000116918			Tsnax (MGI:1855672)			
chr1	231626814	232041271	1q42.1	1q42.2		605210	"DISC1, SCZD9"	Disrupted in schizophrenia 1	DISC1	27185	ENSG00000162946		"{Schizophrenia 9, susceptibility to}, 604906 (3)"	Disc1 (MGI:2447658)			
chr1	231814625	231818516	1q42.1	1q42.2		606271	DISC2	Disrupted in schizophrenia 2	DISC2	27184		noncoding antisense RAN	"Schizophrenia, 181500 (2), Autosomal dominant"				
chr1	232397964	232630490	1q42.2	1q42.2		611609	"SIPA1L2, KIAA1389"	SIPA1-like protein 2	SIPA1L2	57568	ENSG00000116991			Sipa1l2 (MGI:2676970)			
chr1	232984108	233295729	1q42.2	1q42.2		617656	"PCNX2, KIAA0435"	"Pecanex, Drosophila, homolog of, 2"	PCNX2	80003	ENSG00000135749			Pcnx2 (MGI:2445010)			
chr1	233327731	233385147	1q42	1q42.2		614793	"MLK4, KIAA1804"	Mixed-lineage kinase 4	MAP3K21	84451	ENSG00000143674			Map3k21 (MGI:2385307)			
chr1	233614003	233672511	1q42-q43	1q42.2		601745	"KCNK1, TWIK1"	"Potassium channel, subfamily K, member 1"	KCNK1	3775	ENSG00000135750			Kcnk1 (MGI:109322)			
chr1	234373436	234384048	1q42.2	1q42.2		614772	"COA6, C1orf31, CEMCOX4"	Cytochrome c oxidase assembly factor 6	COA6	388753	ENSG00000168275		"Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4, 616501 (3), Autosomal recessive"				
chr1	234391312	234479173	1q42.3	1q42.2		605052	"TARBP1, TRP185"	TAR RNA-binding protein 1	TARBP1	6894	ENSG00000059588			Tarbp1 (MGI:4936930)			
chr1	234604268	234609524	1q42.3	1q42.3		615332	"IRF2BP2, CVID14"	Interferon regulatory factor 2-binding protein 2	IRF2BP2	359948	ENSG00000168264	mutation identified in 1 CVID14 family	"?Immunodeficiency, common variable, 14, 617765 (3), Autosomal dominant"	Irf2bp2 (MGI:2443921)			
chr1	235109340	235128940	1q42.3	1q42.3		601848	"TOMM20, MAS20, KIAA0016"	"Translocase of outer mitochondrial membrane 20, S. cerevisiae, homolog of"	TOMM20	9804	ENSG00000173726			Tomm20 (MGI:1915202)			
chr1	235166894	235328223	1q42.1-q43	1q42.3		609696	"ARID4B, SAP180, RBP1L1, RBBP1L1, BRCAA1"	AT-rich interactive domain-containing protein 4B	ARID4B	51742	ENSG00000054267			Arid4b (MGI:2137512)			
chr1	235328437	235344531	1q43	1q42.3		606982	"GGPS1, GGPPS1"	Geranylgeranyl diphosphate synthase 1	GGPS1	9453	ENSG00000152904			Ggps1 (MGI:1341724)			
chr1	235367359	235448967	1q42-q43	1q42.3		604934	"TBCE, KCS, KCS1, HRD, PEAMO"	Tubulin-specific chaperone E	TBCE	6905	ENSG00000284770		"Encephalopathy, progressive, with amyotrophy and optic atrophy, 617207 (3), Autosomal recessive; Hypoparathyroidism-retardation-dysmorphism syndrome, 241410 (3), Autosomal recessive; Kenny-Caffey syndrome, type 1, 244460 (3), Autosomal recessive"	Tbce (MGI:1917680)			
chr1	235440653	235504480	1q42.3	1q42.3		610194	"B3GALNT2, MGC39558, MDDGA11"	"Beta-1,3-N-acetylgalactosaminyltransferase 2"	B3GALNT2	148789	ENSG00000162885		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11, 615181 (3), Autosomal recessive"	B3galnt2 (MGI:2145517)			
chr1	235547684	235650753	1q42.3	1q42.3		604388	GNG4	"Guanine nucleotide-binding protein, gamma 4"	GNG4	2786	ENSG00000168243			Gng4 (MGI:102703)			
chr1	235661030	235883707	1q42.3	1q42.3		606897	"LYST, CHS1"	Lysosomal trafficking regulator	LYST	1130	ENSG00000143669		"Chediak-Higashi syndrome, 214500 (3), Autosomal recessive"	Lyst (MGI:107448)			
chr1	235975829	236065180	1q43	1q42.3		131390	NID	Nidogen	NID1	4811	ENSG00000116962			Nid1 (MGI:97342)			
chr1	236142528	236213534	1q42-q43	1q42.3		604658	TM7SF1	"Transmembrane 7 superfamily, member 1"	GPR137B	7107	ENSG00000077585			Gpr137b (MGI:1891463)			
chr1	236213063	236282038	1q42.3	1q42.3		615437	ERO1LB	Endoplasmic reticulum oxidoreduction 1-like beta	ERO1B	56605	ENSG00000086619			Ero1lb (MGI:1914725)			
chr1	236394379	236484707	1q42.2-q43	1q42-q43		606603	"EDARADD, ED3, EDA3, ECTD11B, ECTD11A"	EDAR-associated death domain	EDARADD	128178	ENSG00000186197		"Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant, 614940 (3), Autosomal dominant; Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive, 614941 (3), Autosomal recessive"	Edaradd (MGI:1931001)			
chr1	236400000	248956422	1q43-q44			612433	DFNB45	"Deafness, autosomal recessive 45"	DFNB45	449483		between D1S547 and D1S2836	"Deafness, autosomal recessive 45, 612433 (2), Autosomal recessive"				
chr1	236518213	236552980	1q42-q43	1q43		606099	"LGALS8, PCTA1"	"Lectin, galactoside-binding, soluble, 8"	LGALS8	3964	ENSG00000116977			Lgals8 (MGI:1928481)			
chr1	236686453	236764630	1q42-q43	1q43		102573	"ACTN2, CMD1AA, CMH23"	"Actinin, alpha-2"	ACTN2	88	ENSG00000077522		"Cardiomyopathy, dilated, 1AA, with or without LVNC, 612158 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 23, with or without LVNC, 612158 (3), Autosomal dominant"	Actn2 (MGI:109192)			
chr1	236794303	236903980	1q43	1q43		156570	"MTR, HMAG"	5-methyltetrahydrofolate-homocysteine methyltransferase 1	MTR	4548	ENSG00000116984		"Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3), Autosomal recessive; {Neural tube defects, folate-sensitive, susceptibility to}, 601634 (3), Autosomal recessive"	Mtr (MGI:894292)			
chr1	237042207	237833987	1q42.1-q43	1q43		180902	"RYR2, VTSIP, ARVD2, ARVC2"	Ryanodine receptor-2 (cardiac)	RYR2	6262	ENSG00000198626		"Arrhythmogenic right ventricular dysplasia 2, 600996 (3), Autosomal dominant; Ventricular tachycardia, catecholaminergic polymorphic, 1, 604772 (3), Autosomal dominant"	Ryr2 (MGI:99685)			
chr1	237882376	237890921	1q43	1q43		613514	"ZP4, ZPB"	Zona pellucida glycoprotein 4	ZP4	57829	ENSG00000116996						
chr1	239386564	239915449	1q41-q44	1q43		118494	"CHRM3, PBS, EGBRS"	"Cholinergic receptor, muscarinic, 3"	CHRM3	1131	ENSG00000133019	mutation identified in 1 PBS family	"?Prune belly syndrome, 100100 (3), Autosomal recessive"	Chrm3 (MGI:88398)			
chr1	240091884	240475188	1q43	1q43		606373	"FMN2, MRT47"	Formin 2	FMN2	56776	ENSG00000155816		"Mental retardation, autosomal recessive 47, 616193 (3), Autosomal recessive"	Fmn2 (MGI:1859252)			
chr1	240489572	240612371	1q43	1q43		608832	"GREM2, PRDC, STHAG9"	"Gremlin 2 homolog, cystine knot superfamily"	GREM2	64388	ENSG00000180875		"Tooth agenesis, selective, 9, 617275 (3), Autosomal dominant"	Grem2 (MGI:1344367)			
chr1	240775192	241357273	1q43	1q43		602517	RGS7	Regulator of G protein signaling 7	RGS7	6000	ENSG00000182901			Rgs7 (MGI:1346089)			
chr1	241497556	241519784	1q42.1	1q43		136850	"FH, HLRCC, MCUL1, FMRD"	Fumarate hydratase	FH	2271	ENSG00000091483		"Fumarase deficiency, 606812 (3), Autosomal recessive; Leiomyomatosis and renal cell cancer, 150800 (3), Autosomal dominant"	Fh1 (MGI:95530)			
chr1	241531882	241595646	1q43	1q43		603538	KMO	Kynurenine 3-monooxygenase	KMO	8564	ENSG00000117009			Kmo (MGI:2138151)			
chr1	241593149	241640398	1q43	1q43		606695	"OPN3, ECPN"	Opsin 3	OPN3	23596	ENSG00000054277			Opn3 (MGI:1338022)			
chr1	241628863	241635929	1q43	1q43		118825	"CHML, REP2"	Choroideremia-like	CHML	1122	ENSG00000203668			Chml (MGI:101913)			
chr1	241847966	241889938	1q42-q43	1q43		606063	"EXO1, HEX1"	"Exonuclease 1, S. cerevisiae, homolog of"	EXO1	9156	ENSG00000174371			Exo1 (MGI:1349427)			
chr1	241957766	241959061	1q43	1q43		615687	"BECN2, BECN1L1"	Beclin 2	BECN2	441925	ENSG00000196289						
chr1	243124427	243255795	1q44	1q43		613023	"CEP170, KIAA0470"	"Centrosomal protein, 170kD"	CEP170	9859	ENSG00000143702			Cep170 (MGI:1918348)			
chr1	243255417	243503682	1q43-q44	1q43-q44		613524	"SDCCAG8, CCCAP, SLSN7, BBS16"	Serologically defined colon cancer antigen 8	SDCCAG8	10806	ENSG00000054282		"Bardet-Biedl syndrome 16, 615993 (3), Autosomal recessive; Senior-Loken syndrome 7, 613615 (3)"	Sdccag8 (MGI:1924066)			
chr1	243488232	243851078	1q44	1q43-q44		611223	"AKT3, PKBG, MPPH2"	v-Akt murine thymoma viral oncogene homolog 3	AKT3	10000	ENSG00000117020		"Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, 615937 (3), Autosomal dominant"	Akt3 (MGI:1345147)			
chr1	244048938	244057475	1q44	1q44		608433	"ZBTB18, ZNF238, RP58, MRD22"	Zinc finger and BTB domain containing 18	ZBTB18	10472	ENSG00000179456		"Mental retardation, autosomal dominant 22, 612337 (3), Autosomal dominant"	Zbtb18 (MGI:1353609)			
chr1	244408491	244452133	1cen-q12	1q44		103060	ADSS	Adenylosuccinate synthetase (Ade(-)H-complementing)	ADSS	159	ENSG00000035687			Adss (MGI:87948)			
chr1	244452012	244640361	1q44	1q44		617510	"CATSPERE, C10orf101"	"Cation channel, sprem-associated, auxiliary subunit epsilon"	CATSPERE	257044	ENSG00000179397			"Catspere2,Catspere1 (MGI:5589632,MGI:3647531)"			
chr1	244652759	244709033	1q44	1q44		614638	"DESI2, PPPDE1"	Desumoylating isopeptidase 2	DESI2	51029	ENSG00000121644			Desi2 (MGI:1926075)			
chr1	244835305	244845062	1q44	1q44		614698	"COX20, FAM36A"	"Cytochrome c oxidase 20, S. cerevisiae, homolog of"	COX20	116228	ENSG00000203667		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Cox20 (MGI:1913609)			
chr1	244850299	244864524	1q44	1q44		602869	"HNRNPU, HNRPU, SAFA, EIEE54"	Heterogeneous nuclear ribonucleoprotein U	HNRNPU	3192	ENSG00000153187		"Epileptic encephalopathy, early infantile, 54, 617391 (3), Autosomal dominant"	Hnrnpu (MGI:1858195)			
chr1	245154984	245709431	1q44	1q44		614026	KIF26B	Kinesin family member 26B	KIF26B	55083	ENSG00000162849			Kif26b (MGI:2447076)			
chr1	245749339	246507341	1q44	1q44		608783	SMYD3	SET and MYND domain-containing protein 3	SMYD3	64754	ENSG00000185420			Smyd3 (MGI:1916976)			
chr1	246540560	246566262	1q44	1q44		607055	TFB2M	"Transcription factor B2, mitochondrial"	TFB2M	64216	ENSG00000162851			Tfb2m (MGI:107937)			
chr1	246566336	246668586	1q44	1q44		613439	CNST	Consortin	CNST	163882	ENSG00000162852			Cnst (MGI:2445141)			
chr1	246839097	246931977	1q44	1q44		610853	"AHCTF1, ELYS"	AT hook containing transcription factor 1	AHCTF1	25909	ENSG00000153207			Ahctf1 (MGI:1915033)			
chr1	246945546	247008092	1q44	1q44		616348	"ZNF695, SBZF3"	Zinc finger protein 695	ZNF695	57116	ENSG00000197472						
chr1	247121974	247172378	1q44	1q44		194631	ZNF124	Zinc finger protein-124 (HZF-16)	ZNF124	7678	ENSG00000196418			Gm20541 (MGI:5142006)			
chr1	247297412	247333375	1q44	1q44		613911	"ZNF496, NIZP1, ZFP496"	Zinc finger protein 496	ZNF496	84838	ENSG00000162714			Zkscan17 (MGI:2679270)			
chr1	247416155	247449107	1q44	1q44		606416	"NLRP3, CIAS1, FCU, FCAS1, NALP3, PYPAF1, DFNA34, KEFH"	"NLR family, pyrin domain containing 3"	NLRP3	114548	ENSG00000162711		"CINCA syndrome, 607115 (3), Autosomal dominant; Deafness, autosomal dominant 34, with or without inflammation, 617772 (3), Autosomal dominant; Familial cold-induced inflammatory syndrome 1, 120100 (3), Autosomal dominant; Keratoendothelitis fugax hereditaria, 148200 (3), Autosomal dominant; Muckle-Wells syndrome, 191900 (3), Autosomal dominant"	Nlrp3 (MGI:2653833)			
chr1	247672117	247673040	1q44	1q44		611677	OR13G1	"Olfactory receptor, family 13, subfamily G, member 1"	OR13G1	441933	ENSG00000197437			Olfr309 (MGI:3030143)			
chr1	247895586	247896530	1q44	1q44		616729	OR2W3	Olfactory receptor family 2 subfamily W member 3	OR2W3	343171	ENSG00000238243			Olfr322 (MGI:3030156)			
chr1	248739414	248755786	1q44	1q44		617067	LYPD8	LY6/PLAUR domain-containing protein 8	LYPD8	646627	ENSG00000259823			Lypd8 (MGI:1917413)			
chr1	248850003	248860760	1q44	1q44		617758	"ZNF692, AREBP"	Zinc finger protein 692	ZNF692	55657	ENSG00000171163			Zfp692 (MGI:2144276)			
chr1	0	248956422	Chr.1			108420	"SPGF2, ASG"	Spermatogenic failure 2		100653377		inversion of chromosome 1	"Spermatogenic failure 2, 108420 (2), Autosomal dominant"				
chr2	0	12000000	2p25			612396	ALLC	Allantoicase	ALLC	55821	ENSG00000151360	nonfunctional in humans					
chr2	0	23800000	2pter-p24			115800	CTRCT29	"Cataract 29, coralliform"		101867602		between D2S297 and D2S2269	"Cataract 29, coralliform, 115800 (2), Autosomal dominant"				
chr2	0	41500000	2p25-p22			602134	"ETM2, ETM"	"Tremor, hereditary essential, 2"	ETM2	2112		max lod at D2S272	"Essential tremor, hereditary, 2, 602134 (2), Autosomal dominant"				
chr2	0	23800000	2p25-p24			607329	HYT3	"Hypertension, essential, susceptibility to, 3"		387575			"{Hypertension, essential, susceptibility to, 3}, 145500 (2), Multifactorial"				
chr2	0	12000000	2p25			609402	PEE2	Preeclampsia/eclampsia 2		780908			"Preeclampsia/eclampsia 2, 609402 (2)"				
chr2	0	83100000	2p25-p12			101850	PPKP3	"Keratoderma, palmoplantar, punctate type III"				max lod at ACP1 and IGKC	"?Keratoderma, palmoplantar, punctate type 3, 101850 (2), Autosomal dominant"				
chr2	38813	47076	2p25.3	2p25.3		611395	FAM110C	"Family with sequence similarity 110, member C"	FAM110C	642273	ENSG00000184731			Fam110c (MGI:1918813)			
chr2	218135	264865	2p25.3	2p25.3		617314	SH3YL1	SH3 domain- and SYLF domain-containing protein 1	SH3YL1	26751	ENSG00000035115			Sh3yl1 (MGI:1346118)			
chr2	264868	278282	2p25	2p25.3		171500	ACP1	"Acid phosphatase 1, soluble"	ACP1	52	ENSG00000143727			Acp1 (MGI:87881)			
chr2	663876	677467	2p25.3	2p25.3		613220	TMEM18	Transmembrane protein 18	TMEM18	129787	ENSG00000151353						
chr2	1413287	1542726	2p25	2p25.3		606765	"TPO, TPX, TDH2A"	Thyroid peroxidase	TPO	7173	ENSG00000115705		"Thyroid dyshormonogenesis 2A, 274500 (3), Autosomal recessive"	Tpo (MGI:98813)			
chr2	1631886	1744851	2p25.3	2p25.3		605158	"PXDN, D2S448E, KIAA0230, PRG2, PXN, COPOA, ASGD7"	"Peroxidasin, Drosophila, homolog of"	PXDN	7837	ENSG00000130508		"Anterior segment dysgenesis 7, with sclerocornea, 269400 (3), Autosomal recessive"	Pxdn (MGI:1916925)			
chr2	1789112	2331387	2p24	2p25.3		613084	"MYT1L, KIAA1106, MRD39"	Myelin transcription factor 1-like	MYT1L	23040	ENSG00000186487		"Mental retardation, autosomal dominant 39, 616521 (3), Autosomal dominant"	Myt1l (MGI:1100511)			
chr2	3188923	3377931	2p25.2	2p25.3		608998	"EIPR1, TSSC1"	EARP complex and GARP complex interacting protein 1	EIPR1	7260	ENSG00000032389			Eipr1 (MGI:1289332)			
chr2	3379244	3479570	2p25.3	2p25.3		614139	"TRAPPC12, TTC15, PEBAS"	"Trafficking protein particle complex, subunit 12"	TRAPPC12	51112	ENSG00000171853		"Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, 617669 (3), Autosomal recessive"	Trappc12 (MGI:2445089)			
chr2	3497918	3519578	2p25.3	2p25.3		613400	"ADI1, SIPL"	Acireductone dioxygenase 1	ADI1	55256	ENSG00000182551			Adi1 (MGI:2144929)			
chr2	3531812	3558370	2p25	2p25.3		604123	"RNASEH1, PEOB2"	Ribonuclease H1	RNASEH1	246243	ENSG00000171865	pseudogenes on chr. 17 and chr.1	"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2, 616479 (3), Autosomal recessive"	Rnaseh1 (MGI:1335073)			
chr2	3575262	3580918	2p25	2p25.3		603658	"RPS7, DBA8"	Ribosomal protein S7	RPS7	6201	ENSG00000171863		"Diamond-Blackfan anemia 8, 612563 (3), Autosomal dominant"	Rps7 (MGI:1333818)			
chr2	3594831	3644643	2p25.3	2p25.3		612502	"COLEC11, CLK1, 3MC2"	Collectin 11	COLEC11	78989	ENSG00000118004		"3MC syndrome 2, 265050 (3), Autosomal recessive"	Colec11 (MGI:1918943)			
chr2	5692666	5701384	2p25	2p25.2		600898	"SOX11, MRD27"	SRY (sex-determining region Y)-box 11	SOX11	6664	ENSG00000176887		"Mental retardation, autosomal dominant 27, 615866 (3), Autosomal dominant"	Sox11 (MGI:98359)			
chr2	6840416	6866634	2p25.2	2p25.2		611787	CMPK2	"Cytidine monophosphate (UMP-CMP) kinase 2, mitochondrial"	CMPK2	129607	ENSG00000134326			Cmpk2 (MGI:99830)			
chr2	6865732	6898238	2p25.2	2p25.2		607810	"RSAD2, VIPERIN"	Radical S-adenosyl methionine domain containing 2	RSAD2	91543	ENSG00000134321			Rsad2 (MGI:1929628)			
chr2	6900000	16500000	2p25.1-p24.3			609946	DFNB47	"Deafness, neurosensory, autosomal recessive 47"	DFNB47	449489		max lod at D2S1400 and D2S262	"Deafness, neurosensory, autosomal recessive 47, 609946 (2), Autosomal recessive"				
chr2	8681982	8684452	2p25	2p25.1		600386	ID2	"Inhibitor of DNA binding 2, dominant negative"	ID2	3398	ENSG00000115738			Id2 (MGI:96397)			
chr2	8721133	8837638	2p25.1	2p25.1		615759	"KIDINS220, ARMS, SINO"	"Kinase D-interacting substrate, 220kD"	KIDINS220	57498	ENSG00000134313		"Spastic paraplegia, intellectual disability, nystagmus, and obesity, 617296 (3), Autosomal dominant"	Kidins220 (MGI:1924730)			
chr2	8852689	9003749	2p25.1	2p25.1		611949	"MBOAT2, LPCAT4"	Membrane-bound O-acyltransferase domain-containing 2	MBOAT2	129642	ENSG00000143797			Mboat2 (MGI:1914466)			
chr2	9206764	9405682	2p24	2p25.1		603817	"DDEF2, PAP"	Development- and differentiation-enhancing factor 2	ASAP2	8853	ENSG00000151693			Asap2 (MGI:2685438)			
chr2	9405680	9423568	2p25.2	2p25.1		607153	"ITGB1BP1, ICAP1, ICAP1A, ICAP1B"	Integrin cytoplasmic domain-associated protein 1 beta	ITGB1BP1	9270	ENSG00000119185			Itgb1bp1 (MGI:1306802)			
chr2	9488485	9555819	2p25	2p25.1		603639	"ADAM17, TACE, NISBD1"	A disintegrin and metalloproteinase domain 17	ADAM17	6868	ENSG00000151694	mutation identified in 1 NISBD1 family	"?Inflammatory skin and bowel disease, neonatal, 1, 614328 (3), Autosomal recessive"	Adam17 (MGI:1096335)			
chr2	9583966	9631054	2p25.1	2p25.1		609009	TYHAQ	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta isoform"	YWHAQ	10971	ENSG00000134308	pseudogene on chr.22		"Ywhaq,Ywhaq-ps3 (MGI:3650241,MGI:891963)"			
chr2	9843441	9934415	2p25	2p25.1		604904	"RAF1B, RAFI63, SL1"	TATA box-binding protein-associated factor 1B	TAF1B	9014	ENSG00000115750			Taf1b (MGI:109577)			
chr2	9951662	10002283	2p25.1	2p25.1		609786	"GRHL1, LBP32, MGR"	Grainyhead-like 1	GRHL1	29841	ENSG00000134317			Grhl1 (MGI:2182540)			
chr2	10043554	10054835	2p25	2p25.1		603301	"KLF11, TIEG2, FKLF1, FKLF, MODY7"	Kruppel-like factor 11	KLF11	8462	ENSG00000172059		"Maturity-onset diabetes of the young, type VII, 610508 (3)"	Klf11 (MGI:2653368)			
chr2	10122567	10131418	2p25-p24	2p25.1		180390	RRM2	"Ribonucleotide reductase, M2 polypeptide"	RRM2	6241	ENSG00000171848	"pseudogenes on 1p, 1q, Xp"		Rrm2 (MGI:98181)			
chr2	10302123	10427616	2p25.1	2p25.1		600207	HPCAL1	Hippocalcin-like 1	HPCAL1	3241	ENSG00000115756			Hpcal1 (MGI:1855689)			
chr2	10440370	10448553	2p25	2p25.1		165640	ODC1	Ornithine decarboxylase-1	ODC1	4953	ENSG00000115758	pseudogene ODCP on 7q31-qter	"{Colonic adenoma recurrence, reduced risk of}, 114500 (3), Autosomal dominant"	Odc1 (MGI:97402)			
chr2	10570765	10689986	2p25.1	2p25.1		616197	"NOL10, PQBP5"	Nucleolar protein 10	NOL10	79954	ENSG00000115761			Nol10 (MGI:2684913)			
chr2	10783390	10837976	2p25-p24	2p25.1		611099	"PDIA6, ERP5"	"Protein disulfide isomerase, family A, member 6"	PDIA6	10130	ENSG00000143870			Pdia6 (MGI:1919103)			
chr2	10911936	10914224	2p25	2p25.1		603787	"KCNF1, KH1"	"Potassium voltage-gated channel, subfamily F, member 1"	KCNF1	3754	ENSG00000162975			Kcnf1 (MGI:2687399)			
chr2	11179758	11345406	2p24	2p25.1		604002	ROCK2	RHO-associated coiled-coil-containing protein kinase 2	ROCK2	9475	ENSG00000134318			Rock2 (MGI:107926)			
chr2	11481674	11642787	2p25.1	2p25.1		611736	GREB1	GREB1 protein	GREB1	9687	ENSG00000196208			Greb1 (MGI:2149712)			
chr2	11658118	11670205	2p25.1	2p25.1		605538	NTSR2	Neurotensin receptor 2	NTSR2	23620	ENSG00000169006			Ntsr2 (MGI:108018)			
chr2	11677543	11827408	2p21	2p25.1		605518	LPIN1	Lipin 1	LPIN1	23175	ENSG00000134324	related to LSL	"Myoglobinuria, acute recurrent, autosomal recessive, 268200 (3), Autosomal recessive"	Lpin1 (MGI:1891340)			
chr2	12000000	41500000	2p24-p22			610760	CLQTL2	Cholesterol level quantitative trait locus 2		100188817		max lod at D2S1360	"[Cholesterol level QTL 2], 610760 (2)"				
chr2	12000000	23800000	2p24			609800	GEFSP4	"Generalized epilepsy with febrile seizures plus, type 4"		100188796		max lod at D2S305	"Epilepsy, generalized, with febrile seizures plus, type 4, 609800 (2), Autosomal dominant"				
chr2	12000000	23800000	2p24			609271	KTCN4	Keratoconus 4		550624		between D2S305 and D2S2373	"Keratoconus 4, 609271 (2)"				
chr2	14632682	14651915	2p24.3	2p24.3		611234	"FAM84A, NSE1"	"Family with sequence similarity 84, member A"	FAM84A	151354	ENSG00000162981			Fam84a (MGI:2145011)			
chr2	14998066	15561347	2p24-p23	2p24.3		608025	"NBAS, NAG, SOPH, ILFS2"	Neuroblastoma-amplified sequence	NBAS	51594	ENSG00000151779		"Infantile liver failure syndrome 2, 616483 (3), Autosomal recessive; Short stature, optic nerve atrophy, and Pelger-Huet anomaly, 614800 (3), Autosomal recessive"	Nbas (MGI:1918419)			
chr2	15591620	15631110	2p24	2p24.3		601257	DDX1	DEAD/H box-1	DDX1	1653	ENSG00000079785			Ddx1 (MGI:2144727)			
chr2	15920398	15936017	2p24.3	2p24.3		615968	MYCNUT	"MYCN upstream transcript, noncoding"	MYCNUT	103752554							
chr2	15936264	15942458	2p24.1	2p24.3		605374	"MYCNOS, NCYM"	"Oncogene NCYM, opposite strand"	MYCNOS	10408							
chr2	15940437	15947006	2p24.1	2p24.3		164840	"MYCN, NMYC, ODED, MODED"	Oncogene NMYC	MYCN	4613	ENSG00000134323	proximal to APOB	"Feingold syndrome 1, 164280 (3), Autosomal dominant"	Mycn (MGI:97357)			
chr2	16050426	16085688	2p24.3	2p24.3		616132	"GACAT3, LINC01458"	"Gastric cancer-associated transcript 3, noncoding"	GACAT3	104797537							
chr2	17540539	17656438	2p	2p24.2		600817	VSNL1	Visinin-like 1	VSNL1	7447	ENSG00000163032			Vsnl1 (MGI:1349453)			
chr2	17663811	17753832	2p24.2	2p24.2		609387	"SMC6L1, SMC6"	Structural maintenance of chromosomes 6-like 1	SMC6	79677	ENSG00000163029			Smc6 (MGI:1914491)			
chr2	17753686	17785919	2p24.2	2p24.2		612449	GEN1	"GEN1, Drosophila, homolog of"	GEN1	348654	ENSG00000178295			Gen1 (MGI:2443149)			
chr2	17816509	17817797	2p24.2	2p24.2		612209	MSGN1	Mesogenin 1	MSGN1	343930	ENSG00000151379			Msgn1 (MGI:1860483)			
chr2	17877846	17932960	2p24	2p24.2		603888	"KCNS3, KV9.3"	"Potassium voltate-gated channel, delayed-rectifier, subfamily S, member 3"	KCNS3	3790	ENSG00000170745			Kcns3 (MGI:1098804)			
chr2	18554722	18560692	2p24.2	2p24.2		616796	"RDH14, SDR7C4, PAN2"	Retinol dehydrogenase 14	RDH14	57665	ENSG00000240857			Rdh14 (MGI:1920402)			
chr2	18562870	18589579	2p24.2	2p24.2		610526	"NT5C1B, CN1B, AIRP"	"5'-nucleotidase, cytosolic, Ib"	NT5C1B	93034	ENSG00000185013			Nt5c1b (MGI:1918131)			
chr2	19351484	19358610	2p24	2p24.1		608891	"ODD, OSR1"	"ODD-skipped, Drosophila, homolog of"	OSR1	130497	ENSG00000143867			Osr1 (MGI:1344424)			
chr2	19910259	19990122	2p24.1	2p24.1		613602	"WDR35, NAOFEN, KIAA1336, CED2, SRTD7"	WD repeat-containing protein 35	WDR35	57539	ENSG00000118965		"Cranioectodermal dysplasia 2, 613610 (3), Autosomal recessive; Short-rib thoracic dysplasia 7 with or without polydactyly, 614091 (3), Autosomal recessive"	Wdr35 (MGI:1921932)			
chr2	19992051	20012693	2p24-p23	2p24.1		602109	"MATN3, EDM5, HOA, OS2"	Matrilin 3	MATN3	4148	ENSG00000132031	mutation identified in 1 SEMDM family	"Epiphyseal dysplasia, multiple, 5, 607078 (3), Autosomal dominant; {Osteoarthritis susceptibility 2}, 140600 (3), Autosomal dominant; ?Spondyloepimetaphyseal dysplasia, 608728 (3), Autosomal recessive"	Matn3 (MGI:1328350)			
chr2	20200796	20225432	2p24.1	2p24.1		186355	SDC1	Syndecan 1	SDC1	6382	ENSG00000115884	close to NMYC in mouse		Sdc1 (MGI:1349162)			
chr2	20248690	20352427	2p22-p21	2p24.1		607205	"PUM2, KIAA0235"	"Pumilio, Drosophila, homolog of, 2"	PUM2	23369	ENSG00000055917			Pum2 (MGI:1931751)			
chr2	20447070	20449444	2p24.1	2p24.1		165370	"RHOB, ARHB, ARH6, RHOH6"	"RAS homolog gene family, member B (oncogene RHO H6)"	RHOB	388	ENSG00000143878			Rhob (MGI:107949)			
chr2	20552933	20651660	2p24.1	2p24.1		609359	"HS1BP3, FLJ14249, ETM2"	HS1-binding protein 3	HS1BP3	64342	ENSG00000118960			Hs1bp3 (MGI:1913224)			
chr2	20666663	20679242	2p24-p23	2p24.1		604651	GDF7	Growth/differentiation factor 7	GDF7	151449	ENSG00000143869			Gdf7 (MGI:95690)			
chr2	20682488	20823138	2p24.1	2p24.1		613570	"LDAH, C2orf43"	Lipid droplet associated hydrolase	LDAH	60526	ENSG00000118961			Ldah (MGI:1916082)			
chr2	21001428	21044072	2p24	2p24.1		107730	"APOB, FLDB, LDLCQ4"	Apolipoprotein B (including Ag(x) antigen)	APOB	338	ENSG00000084674	1 gene for liver apo-B100 and gut apo-B48; Ag linked	"Hypercholesterolemia, due to ligand-defective apo B, 144010 (3), Autosomal dominant; Hypobetalipoproteinemia, 615558 (3), Autosomal recessive"	Apob (MGI:88052)			
chr2	23687623	23927113	2p24.1-p23.3	2p24.1-p23.3		615347	"ATAD2B, KIAA1240"	"ATPase family, AAA domain-containing, member 2B"	ATAD2B	54454	ENSG00000119778			Atad2b (MGI:2444798)			
chr2	23800000	36300000	2p23.3-p22.3			609955	"GINGF3, HGF3, GGF3"	"Fibromatosis, gingival, 3"	GINGF3	780916		between D2S2221 and D2S1788	"Fibromatosis, gingival, 3, 609955 (2)"				
chr2	24009021	24026774	2p23.3	2p23.3		617845	MFSD2B	Major facilitator superfamily domain-containing protein 2B	MFSD2B	388931	ENSG00000205639			Mfsd2b (MGI:3583946)			
chr2	24029335	24047425	2p23.3	2p23.3		616234	"C2orf44, WDCP"	WD repeat- and coiled-coil-containing protein	WDCP	80304	ENSG00000163026			Wdcp (MGI:3040699)			
chr2	24033204	24067742	2p23.3	2p23.3		600620	"FKBP1B, PKBP1L"	FK506-binding protein 1B	FKBP1B	2281	ENSG00000119782			Fkbp1b (MGI:1336205)			
chr2	24067583	24076443	2p25	2p23.3		607835	"SAP14, SF3B14, P14"	"Spliceosome-associated protein, 14kD"	SF3B6	51639	ENSG00000115128			Sf3b6 (MGI:1913305)			
chr2	24077427	24085766	2p23.3	2p23.3		605171	"TP53I3, PIG3"	Tumor protein p53-inducible protein 3	TP53I3	9540	ENSG00000115129						
chr2	24202863	24360537	2p25	2p23.3		604464	"ITSN2, SH3D1B, SWAP, KIAA1256"	Intersectin 2	ITSN2	50618	ENSG00000198399			Itsn2 (MGI:1338049)			
chr2	24492049	24770701	2p23	2p23.3		602691	"NCOA1, SRC1"	Nuclear receptor coactivator 1	NCOA1	8648	ENSG00000084676			Ncoa1 (MGI:1276523)			
chr2	24790266	24793381	2p23.3	2p23.3		617342	"PRTHD1, C2orf79"	Peptidyl-tRNA hydrolase domain-containing 1	PTRHD1	391356	ENSG00000184924			Ptrhd1 (MGI:1916959)			
chr2	24793114	24822375	2p23.3	2p23.3		611504	CENPO	Centromeric protein O	CENPO	79172	ENSG00000138092			Cenpo (MGI:1923800)			
chr2	24819168	24920016	2p24-p22	2p23.3		600291	"ADCY3, BMIQ19"	Adenylate cyclase-3	ADCY3	109	ENSG00000138031		"{Obesity, susceptibility to, BMIQ19}, 617885 (3)"	Adcy3 (MGI:99675)			
chr2	24943635	24972093	2p23.3	2p23.3		613527	"DNAJC27, RBJ"	"DNAJ/HSP40 homolog, subfamily, C, member 27"	DNAJC27	51277	ENSG00000115137			Dnajc27 (MGI:2443036)			
chr2	25042103	25159136	2p23.3	2p23.3		616797	"EFR3B, KIAA0953"	"Efr3, S. cerevisiae, homolog of, B"	EFR3B	22979	ENSG00000084710			Efr3b (MGI:2444851)			
chr2	25160852	25168850	2p23.3	2p23.3		176830	"POMC, OBAIRH"	Proopiomelanocortin (adrenocorticotropin/beta-lipotropin)	POMC	5443	ENSG00000115138		"Obesity, adrenal insufficiency, and red hair due to POMC deficiency, 609734 (3), Autosomal recessive; {Obesity, early-onset, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Pomc (MGI:97742)			
chr2	25232960	25342589	2p23	2p23.3		602769	"DNMT3A, TBRS"	DNA methyltransferase 3A	DNMT3A	1788	ENSG00000119772		"Acute myeloid leukemia, somatic, 601626 (3); Tatton-Brown-Rahman syndrome, 615879 (3), Autosomal dominant"	Dnmt3a (MGI:1261827)			
chr2	25377242	25673673	2p23-p22	2p23.3		602415	DTNB	"Dystrobrevin, beta"	DTNB	1838	ENSG00000138101			Dtnb (MGI:1203728)			
chr2	25733752	25878515	2p23.3	2p23.3		612991	"ASXL2, KIAA1685, SHAPNS"	Additional sex combs-like 2	ASXL2	55252	ENSG00000143970		"Shashi-Pena syndrome, 617190 (3), Autosomal dominant"	Asxl2 (MGI:1922552)			
chr2	25926585	25982739	2p23	2p23.3		602845	KIF3C	Kinesin family member 3C	KIF3C	3797	ENSG00000084731			Kif3c (MGI:107979)			
chr2	26033859	26137453	2p23.3	2p23.3		612672	RAB10	Ras-associated protein	RAB10	10890	ENSG00000084733			Rab10 (MGI:105066)			
chr2	26190634	26244725	2p23	2p23.3		600890	"HADHA, MTPA"	"Hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/ enoyl-Coenzyme A hydratase (trifunctional protein), alpha subunit"	HADHA	3030	ENSG00000084754		"Fatty liver, acute, of pregnancy, 609016 (3), Autosomal recessive; HELLP syndrome, maternal, of pregnancy, 609016 (3), Autosomal recessive; LCHAD deficiency, 609016 (3), Autosomal recessive; Trifunctional protein deficiency, 609015 (3), Autosomal recessive"	Hadha (MGI:2135593)			
chr2	26244747	26290464	2p23	2p23.3		143450	HADHB	"Hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase /enoyl-Coenzyme A hydratase (trifunctional protein), beta subunit"	HADHB	3032	ENSG00000138029		"Trifunctional protein deficiency, 609015 (3), Autosomal recessive"	Hadhb (MGI:2136381)			
chr2	26346085	26395890	2p23.3	2p23.3		607915	"SELENOI, SELI"	Selenoprotein I	SELENOI	85465	ENSG00000138018			Selenoi (MGI:107898)			
chr2	26401911	26456712	2p23.3	2p23.3		615288	"DRC1, CCDC164, C2orf39, CILD21"	"Dynein regulatory complex, subunit 1, Chlamydomonas, homolog of"	DRC1	92749	ENSG00000157856		"Ciliary dyskinesia, primary, 21, 615294 (3), Autosomal recessive"	Drc1 (MGI:2685906)			
chr2	26457202	26558697	2p23-p22	2p23.3		603681	"OTOF, DFNB9, NSRD9, AUNB1"	Otoferlin	OTOF	9381	ENSG00000115155	symbolized DFNB6 by authors	"Auditory neuropathy, autosomal recessive, 1, 601071 (3), Autosomal recessive; Deafness, autosomal recessive 9, 601071 (3), Autosomal recessive"	Otof (MGI:1891247)			
chr2	26692712	26733419	2p23	2p23.3		603220	"KCNK3, TASK, PPH4"	"Potassium channel, subfamily K, member 3"	KCNK3	3777	ENSG00000171303		"Pulmonary hypertension, primary, 4, 615344 (3), Autosomal dominant"	Kcnk3 (MGI:1100509)			
chr2	26786013	26794588	2p24-p21	2p23.3		117139	CENPA	"Centromere protein A, 17kD"	CENPA	1058	ENSG00000115163			Cenpa (MGI:88375)			
chr2	26848100	26950350	2p23.3	2p23.3		608383	"DPYSL5, CRMP5, CRAM"	Dihydropyrimidinase-like 5	DPYSL5	56896	ENSG00000157851			Dpysl5 (MGI:1929772)			
chr2	26970370	27027218	2p23.3-p23.1	2p23.3		605788	"MAPRE3, EB3, RP3, EBF3"	"Microtubule-associated protein, RP/EB family, member 3"	MAPRE3	22924	ENSG00000084764			Mapre3 (MGI:2140967)			
chr2	27032905	27041696	2p23.3	2p23.3		615301	TMEM214	Transmembrane protein 214	TMEM214	54867	ENSG00000119777			Tmem214 (MGI:1916046)			
chr2	27051422	27070621	2p23.3	2p23.3		615900	"AGBL5, CCP5, RP75"	AATP/GTP-binding protein-like 5	AGBL5	60509	ENSG00000084693		"Retinitis pigmentosa 75, 617023 (3), Autosomal recessive"	Agbl5 (MGI:2441745)			
chr2	27078566	27086402	2p23.3-p23.2	2p23.3		130660	"EMILIN1, EMILIN"	Elastin microfibril interfacer 1	EMILIN1	11117	ENSG00000138080			Emilin1 (MGI:1926189)			
chr2	27086742	27100750	2p23.3-p23.2	2p23.3		614058	KHK	Ketohexokinase (fructokinase)	KHK	3795	ENSG00000138030		"[Fructosuria], 229800 (3), Autosomal recessive"	Khk (MGI:1096353)			
chr2	27099352	27119126	2p23.3	2p23.3		606137	"CGREF1, CGR11"	Cell growth regulator with EF-hand domain 1	CGREF1	10669	ENSG00000138028			Cgref1 (MGI:1915817)			
chr2	27123779	27131113	2p23.3	2p23.3		612195	"ABHD1, LABH1"	Abhydrolase domain-containing 1	ABHD1	84696	ENSG00000143994						
chr2	27130755	27134674	2p23	2p23.3		606395	PREB	Prolactin regulatory element-binding protein	PREB	10113	ENSG00000138073			Preb (MGI:1355326)			
chr2	27148891	27153585	2p24-p23	2p23.3		609635	TCF23	Transcription factor 23	TCF23	150921	ENSG00000163792			Tcf23 (MGI:1934960)			
chr2	27199586	27212341	2p23.3	2p23.3		604024	"SLC5A6, SMVT"	"Solute carrier family 5 (sodium dependent vitamin transporter), member 6"	SLC5A6	8884	ENSG00000138074			Slc5a6 (MGI:2660847)			
chr2	27217389	27243791	2p21	2p23.3		114010	"CAD, CDG1Z, EIEE50"	CAD trifunctional protein of pyrimidine biosynthesis	CAD	790	ENSG00000084774		"Epileptic encephalopathy, early infantile, 50, 616457 (3), Autosomal recessive"	Cad (MGI:1916969)			
chr2	27254571	27275862	2p23.3	2p23.3		602878	"SLC30A3, ZNT3"	"Solute carrier family 30 (zinc transporter), member 3"	SLC30A3	7781	ENSG00000115194			Slc30a3 (MGI:1345280)			
chr2	27275420	27281429	2p23.3	2p23.3		613946	DNAJC5G	"DNAJ/HSP40 homolog, subfamily C, member 5, gamma"	DNAJC5G	285126	ENSG00000163793			Dnajc5g (MGI:3045263)			
chr2	27282428	27307438	2p23.3	2p23.3		606474	"TRIM54, RNF30, MURF3"	Tripartite motif containing 54	TRIM54	57159	ENSG00000138100			Trim54 (MGI:1889623)			
chr2	27307399	27308444	2p23-p21	2p23.3		600945	"UCN, UROC"	Urocortin	UCN	7349	ENSG00000163794			Ucn (MGI:1276123)			
chr2	27309491	27323101	2p23-p21	2p23.3		137960	"MPV17, MTDPS6"	"Mpv17 transgene, mouse, glomerulosclerosis, homolog of"	MPV17	4358	ENSG00000115204		"Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810 (3), Autosomal recessive"	Mpv17 (MGI:97138)			
chr2	27364351	27370456	2p23.3	2p23.3		606687	EIF2B4	"Eukaryotic translation initiation factor 2B, subunit 4"	EIF2B4	8890	ENSG00000115211		"Leukoencephalopathy with vanishing white matter, 603896 (3), Autosomal recessive; Ovarioleukodystrophy, 603896 (3), Autosomal recessive"	Eif2b4 (MGI:95300)			
chr2	27370495	27377532	2p23-p22	2p23.3		605963	SNX17	Sorting nexin 17	SNX17	9784	ENSG00000115234			Snx17 (MGI:2387801)			
chr2	27377230	27380865	2p24.1-p22.3	2p23.3		613598	"ZNF513, RP58"	Zinc finger protein 513	ZNF513	130557	ENSG00000163795	mutation identified in 1 RP58 family	"?Retinitis pigmentosa 58, 613617 (3), Autosomal recessive"	Zfp513 (MGI:2141255)			
chr2	27381198	27409682	2p23.3	2p23.3		605119	"PPM1G, PP2CG"	"Protein phosphatase, magnesium/manganese-dependent, 1G"	PPM1G	5496	ENSG00000115241			Ppm1g (MGI:106065)			
chr2	27427789	27442258	2p23	2p23.3		606010	NRBP	Nuclear receptor-binding protein	NRBP1	29959	ENSG00000115216			Nrbp1 (MGI:2183436)			
chr2	27444372	27489818	2p23.3	2p23.3		607386	"IFT172, SLB, KIAA1179, SRTD10, RP71"	"Intraflagellar transport 172, Chlamydomonas, homolog of"	IFT172	26160	ENSG00000138002		"Retinitis pigmentosa 71, 616394 (3), Autosomal recessive; Short-rib thoracic dysplasia 10 with or without polydactyly, 615630 (3), Autosomal recessive"	Ift172 (MGI:2682064)			
chr2	27491882	27495501	2p23.3	2p23.3		611905	"FNDC4, FRCP1"	Fibronectin type III domain-containing protein 4	FNDC4	64838	ENSG00000115226			Fndc4 (MGI:1917195)			
chr2	27496838	27523688	2p23.3-p23.2	2p23.3		600842	"GCKR, GKRP, FGQTL5"	Glucokinase (hexokinase 4) regulatory protein	GCKR	2646	ENSG00000084734		"[Fasting plasma glucose level QTL 5], 613463 (3)"	Gckr (MGI:1096345)			
chr2	27628647	27650845	2p23.3	2p23.3		611479	"XAB1, MBDIN"	XPA-binding protein	GPN1	11321	ENSG00000198522			Gpn1 (MGI:1921504)			
chr2	27642567	27663839	2p25	2p23.3		612762	"SUPT7L, SUPT7H, SPT7l, KIAA0764, STAF65G"	Suppressor of TY 7-like	SUPT7L	9913	ENSG00000119760			Supt7l (MGI:1919445)			
chr2	27663470	27694979	2p23.3-p23.2	2p23.3		602655	SLC4A1AP	"Solute carrier family 4 (anion exchanger), member 1, adaptor protein"	SLC4A1AP	22950	ENSG00000163798			Slc4a1ap (MGI:1196608)			
chr2	27771716	27779740	2p22	2p23.2		610059	MRPL33	Mitochondrial ribosomal protein L33	MRPL33	9553	ENSG00000243147			Mrpl33 (MGI:2137225)			
chr2	27781363	27890395	2p23.2	2p23.2		611132	RBKS	Ribokinase	RBKS	64080	ENSG00000171174			Rbks (MGI:1918586)			
chr2	27888708	28338900	2p23.2	2p23.2		610497	"BRE, BRCC4, BRCC45"	Brain and reproductive organ-expressed protein	BABAM2	9577	ENSG00000158019			Babam2 (MGI:1333875)			
chr2	28392854	28417311	2p23.2	2p23.2		601575	FOSL2	FOS-like antigen-2	FOSL2	2355	ENSG00000075426			Fosl2 (MGI:102858)			
chr2	28488577	28644134	2p23.2	2p23.2		610179	"PLB1, PLB, FLJ30866"	Phospholipase B1	PLB1	151056	ENSG00000163803			Plb1 (MGI:1922406)			
chr2	28751747	28802939	2p23	2p23.2		600590	"PPP1CB, NSLH2"	"Protein phosphatase-1, catalytic subunit, beta isoform"	PPP1CB	5500	ENSG00000213639		"Noonan syndrome-like disorder with loose anagen hair 2, 617506 (3), Autosomal dominant"	Ppp1cb (MGI:104871)			
chr2	28810833	28850609	2p23.2	2p23.2		614029	"SPDYA, SPY1, RINGOA"	"Speedy, xenopus, homolog of, A"	SPDYA	245711	ENSG00000163806			Spdya (MGI:1918141)			
chr2	28894642	28948219	2p23.2	2p23.2		616195	"WDR43, UTP5, KIAA0007"	WD repeat-containing protein 43	WDR43	23160	ENSG00000163811			Wdr43 (MGI:1919765)			
chr2	29061689	29074260	2p24.1-p23.1	2p23.2		613425	C2orf71	Chromosome 2 open reading frame 71	C2orf71	388939	ENSG00000179270		"Retinitis pigmentosa 54, 613428 (3)"	BC027072 (MGI:2385061)			
chr2	29190991	29921610	2p23	2p23.2-p23.1		105590	"ALK, NBLST3"	Anaplastic lymphoma kinase (Ki-1)	ALK	238	ENSG00000171094		"{Neuroblastoma, susceptibility to, 3}, 613014 (3)"	Alk (MGI:103305)			
chr2	30146567	30160532	2p23.1	2p23.1		609726	YPEL5	Yippee-like 5	YPEL5	51646	ENSG00000119801			Ypel5 (MGI:1916937)			
chr2	30231530	30260032	2p23.1	2p23.1		611763	LBH	"Limb bud and heart development, mouse, homolog of"	LBH	81606	ENSG00000213626			Lbh (MGI:1925139)			
chr2	30447225	30644224	2p23.1	2p23.1		614241	"LCLAT1, ALCAT1, AGPAT8"	Lysocardiolipin acyltransferase 1	LCLAT1	253558	ENSG00000172954			Lclat1 (MGI:2684937)			
chr2	30888517	31138725	2p23.2	2p23.1		608225	GALNT14	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14	GALNT14	79623	ENSG00000158089			Galnt14 (MGI:1918935)			
chr2	31234013	31269450	2p21	2p23.1		605891	EHD3	EH domain-containing 3	EHD3	30845	ENSG00000013016			Ehd3 (MGI:1928900)			
chr2	31334319	31414776	2p23-p22	2p23.1		607633	"XDH, XAN1"	Xanthine dehydrogenase (xanthine oxidase)	XDH	7498	ENSG00000158125		"Xanthinuria, type I, 278300 (3), Autosomal recessive"	Xdh (MGI:98973)			
chr2	31522485	31665650	2p23	2p23.1		607306	SRD5A2	"Steroid-5-alpha-reductase, alpha polypeptide-2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha-2)"	SRD5A2	6716	ENSG00000277893		"Pseudovaginal perineoscrotal hypospadias, 264600 (3), Autosomal recessive"	Srd5a2 (MGI:2150380)			
chr2	31800000	47500000	2p22.3-p21			114580	"CANDF1, CMCT"	"Candidiasis, familial, 1"		117084		between D2S367 and D2S2240	"Candidiasis, familial, 1, autosomal dominant, 114580 (2), Autosomal dominant"				
chr2	31867187	32011051	2p22-p21	2p22.3		611786	"MEMO1, MEMO, C2orf4"	Mediator of cell motility 1	MEMO1	51072	ENSG00000162959			Memo1 (MGI:1924140)			
chr2	32011648	32039839	2p22.3	2p22.3		612032	DPY30	"DPY30, C. elegans, homolog of"	DPY30	84661	ENSG00000162961			Dpy30 (MGI:1913560)			
chr2	32063550	32157636	2p22-p21	2p22.3		604277	"SPAST, SPG4"	Spastin	SPAST	6683	ENSG00000021574		"Spastic paraplegia 4, autosomal dominant, 182601 (3), Autosomal dominant"	Spast (MGI:1858896)			
chr2	32165840	32224378	2p22-p21	2p22.3		611148	"SLC30A6, ZNT6"	"Solute carrier family 30 (zinc transporter), member 6"	SLC30A6	55676	ENSG00000152683			Slc30a6 (MGI:2386741)			
chr2	32224448	32265742	2p22.3	2p22.3		606831	"NLRC4, CARD12, CLAN, IPAF, AIFEC, FCAS4"	"NLR family, caspase recruitment domain-containing 4"	NLRC4	58484	ENSG00000091106	mutation identified in 1 FCAS4 family	"Autoinflammation with infantile enterocolitis, 616050 (3), Autosomal dominant; ?Familial cold autoinflammatory syndrome 4, 616115 (3), Autosomal dominant"	Nlrc4 (MGI:3036243)			
chr2	32277888	32307397	2p22.3	2p22.3		617534	YIPF4	"Yip1 domain family, member 4"	YIPF4	84272	ENSG00000119820			Yipf4 (MGI:1915114)			
chr2	32356906	32618898	2p22-p21	2p22.3		605638	"BIRC6, KIAA1289"	Baculoviral IAP repeat-containing protein-6	BIRC6	57448	ENSG00000115760			Birc6 (MGI:1276108)			
chr2	32532152	32532245	2p22.3	2p22.3		616473	MIR558	Micro RNA 558	MIR558	693143		BIRC6 is host gene					
chr2	32902128	33399508	2p12-q22	2p22.3		150390	LTBP1	Latent transforming growth factor beta binding protein 1	LTBP1	4052	ENSG00000049323			Ltbp1 (MGI:109151)			
chr2	36300000	38300000	2p22.2			602499	MACOM	"Macrophthalmia, colobomatous, with microcornea"					"Macrophthalmia, colobomatous, with microcornea, 602499 (4), Autosomal dominant"				
chr2	36356087	36551134	2p22-p21	2p22.2		606189	CRIM1	Cysteine-rich motor neuron protein 1	CRIM1	51232	ENSG00000150938			Crim1 (MGI:1354756)			
chr2	36552238	36598189	2p22.2	2p22.2		604826	FEZ2	Fasciculation and elongation protein zeta 2	FEZ2	9637	ENSG00000171055			Fez2 (MGI:2675856)			
chr2	36696689	36814793	2p22.2	2p22.2		617693	"VIT, VIT1"	Vitrin	VIT	5212	ENSG00000205221			Vit (MGI:1921449)			
chr2	36837697	36966606	2p22	2p22.2		614765	STRN	"Striatin, calmodulin-binding protein"	STRN	6801	ENSG00000115808			Strn (MGI:1333757)			
chr2	37099209	37157064	2p21	2p22.2		176871	PRKR	"Protein kinase, interferon-inducible double stranded RNA dependent"	EIF2AK2	5610	ENSG00000055332			Eif2ak2 (MGI:1353449)			
chr2	37167819	37196081	2p22.3	2p22.2		617152	SULT6B1	"Sulfotransferase family 6B, member 1"	SULT6B1	391365	ENSG00000138068			Sult6b1 (MGI:1920921)			
chr2	37201628	37231596	2p22.2	2p22.2		612828	"CEBPZ, CBF, NOC1"	"CCAAT/enhancer-binding protein, zeta"	CEBPZ	10153	ENSG00000115816			Cebpz (MGI:109386)			
chr2	37231630	37271364	2p22.2	2p22.2		615898	"NDUFAF7, MIDA"	"NADH dehydrogenase (ubiquinone) complex I, assembly factor 7"	NDUFAF7	55471	ENSG00000003509			Ndufaf7 (MGI:1920944)			
chr2	37250501	37324784	2p21	2p22.2		607077	PRKCN	"Protein kinase C, nu"	PRKD3	23683	ENSG00000115825			Prkd3 (MGI:1922542)			
chr2	37344609	37373321	2p22.2	2p22.2		607065	"QPCT, QC"	Glutaminyl-peptide cyclotransferase	QPCT	25797	ENSG00000115828			Qpct (MGI:1917786)			
chr2	37641881	37672534	2p21	2p22.2		606133	"CDC42EP3, CEP3, BORG2"	CDC42 effector protein 3	CDC42EP3	10602	ENSG00000163171			Cdc42ep3 (MGI:2384718)			
chr2	37920788	38069245	2p22.2	2p22.2		611872	"FAM82A1, FAM82A, RMD2"	"Family with sequence similarity 82, member A1"	RMDN2	151393	ENSG00000115841			Rmdn2 (MGI:2147043)			
chr2	38067602	38076180	2p22-p21	2p22.2		601771	"CYP1B1, GLC3A, ASGD6"	"Cytochrome P450, subfamily I, dioxin-inducible, polypeptide 1"	CYP1B1	1545	ENSG00000138061		"Anterior segment dysgenesis 6, multiple subtypes, 617315 (3); Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3), Autosomal recessive"	Cyp1b1 (MGI:88590)			
chr2	38293956	38378583	2p22.3	2p22.2-p22.1		609368	"ARL3IP2, ATL2"	ADP-ribosylation-like factor 6-interacting protein 2 (atlastin 2)	ATL2	64225	ENSG00000119787			Atl2 (MGI:1929492)			
chr2	38300000	47500000	2p22.1-p21			614227	HNFJ3	"Hyperuricemic nephropathy, familial juvenile, 3"		100689490		between rs372139 and rs896986	"Hyperuricemic nephropathy, familial juvenile, 3, 614227 (2), Autosomal dominant"				
chr2	38563185	38603035	2p22	2p22.1		611208	"HNRNPLL, HNRPLL, SRRF"	Heterogeneous nuclear ribonucleoprotein L-like	HNRNPLL	92906	ENSG00000143889			Hnrnpll (MGI:1919942)			
chr2	38665909	38734766	2p22-p11	2p22.1		137030	"GALM, GLAT"	Galactose mutarotase	GALM	130589	ENSG00000143891			Galm (MGI:2442420)			
chr2	38743598	38751493	2p22-p21	2p22.1		600572	"SRSF7, SFRS7"	"Splicing factor, arginine/serine-rich 7, 35kD"	SRSF7	6432	ENSG00000115875			Srsf7 (MGI:1926232)			
chr2	38778184	38781964	2p22.1	2p22.1		607006	GEMIN6	GEM-associated protein 6	GEMIN6	79833	ENSG00000152147			"Gemin6-ps,Gemin6 (MGI:1914492,MGI:3645567)"			
chr2	38981548	39124958	2p22-p21	2p22.1		182530	"SOS1, GINGF, GF1, HGF, NS4"	"Son of sevenless, Drosophila, homolog of, 1"	SOS1	6654	ENSG00000115904	mutation identified in 1 GINGF1 family	"?Fibromatosis, gingival, 1, 135300 (3), Autosomal dominant; Noonan syndrome 4, 610733 (3), Autosomal dominant"	Sos1 (MGI:98354)			
chr2	39248940	39437311	2p22.1	2p22.1		604921	"MAP4K3, GLK"	Mitogen-activated protein kinase kinase kinase kinase 3	MAP4K3	8491	ENSG00000011566			Map4k3 (MGI:2154405)			
chr2	39736059	39779275	2p22-p21	2p22.1		611751	"THUMPD2, C2orf8"	THUMP domain-containing 2	THUMPD2	80745	ENSG00000138050			Thumpd2 (MGI:1919417)			
chr2	40112116	40512451	2p23-p22	2p22.1		182305	"SLC8A1, NCX1"	"Solute carrier family 8, member 1 (sodium-calcium exchanger-1)"	SLC8A1	6546	ENSG00000183023			Slc8a1 (MGI:107956)			
chr2	41500000	47500000	2p21			606407	"DEL2p21, C2DELp21"	Homozygous 2p21 deletion syndrome				contiguous gene syndrome disrupting SLC3A1 and PREPL genes	"Hypotonia-cystinuria syndrome, 606407 (4), Autosomal recessive"				
chr2	41500000	83100000	2p21-p12			615654	DFNA58	"Deafness, autosomal dominant 58"	DFNA58	100359395		between D2S2259 and D2S2114	"Deafness, autosomal dominant 58, 615654 (2), Autosomal dominant"				
chr2	41500000	47500000	2p21			601694	"LEPQTL1, LSL"	Leptin serum levels quantitative trait locus 1		7839			"[Leptin serum levels QTL1], 601694 (2)"				
chr2	41500000	74800000	2p21-p13			608703	SCA25	Spinocerebellar ataxia 25	SCA25	338435			"Spinocerebellar ataxia 25, 608703 (2), Autosomal dominant"				
chr2	42048020	42058527	2p21	2p21		614150	"PKDCC, VLK, SGK493"	"Protein kinase domain-containing protein, cytoplasmic, mouse, homolog of"	PKDCC	91461	ENSG00000162878			Pkdcc (MGI:2147077)			
chr2	42169337	42332547	2p22-p21	2p21		607442	"EML4, ROPP120"	Echinoderm microtubule associated protein like-4	EML4	27436	ENSG00000143924			Eml4 (MGI:1926048)			
chr2	42335560	42368956	2p21	2p21		605771	"COX7A2L, COX7RP, EB1"	"Cytochrome c oxidase subunit VIIA, polypeptide 2-like"	COX7A2L	9167	ENSG00000115944			Cox7a2l (MGI:106015)			
chr2	42442016	42494096	2p21	2p21		606767	"KCNG3, KV6.3"	"Potassium voltage-gated channel, subfamily G, member 3"	KCNG3	170850	ENSG00000171126			Kcng3 (MGI:2663923)			
chr2	42767086	42801001	2p21	2p21		604521	"HAAO, VCRL1"	"3-hydroxyanthranilate 3,4-dioxygenase"	HAAO	23498	ENSG00000162882		"Vertebral, cardiac, renal, and limb defects syndrome 1, 617660 (3), Autosomal recessive"	Haao (MGI:1349444)			
chr2	43222401	43226605	2p21	2p21		612053	"ZFP36L2, ERF2, TIS11D"	Zinc finger protein 36-like 2	ZFP36L2	678	ENSG00000152518	incorrectly mapped to 6p21.3		Zfp36l2 (MGI:107945)			
chr2	43230835	43596045	2p21	2p21		611800	"THADA, KIAA1767"	Thyroid adenoma-associated gene	THADA	63892	ENSG00000115970			Thada (MGI:3039623)			
chr2	43637299	43767986	2p21	2p21		612723	PLEKHH2	"Pleckstrin homology domain-containing protein, family H, member 2"	PLEKHH2	130271	ENSG00000152527			Plekhh2 (MGI:2146813)			
chr2	43774038	43828319	2p25.1-p24.1	2p21		617083	"DYNC2LI1, D2LIC, LIC3, SRTD15"	"Dynein, cytoplasmic 2, light intermediate chain 1"	DYNC2LI1	51626	ENSG00000138036		"Short-rib thoracic dysplasia 15 with polydactyly, 617088 (3), Autosomal recessive"	Dync2li1 (MGI:1913996)			
chr2	43806153	43838839	2p21	2p21		605459	ABCG5	"ATP-binding cassette, subfamily G, member 5"	ABCG5	64240	ENSG00000138075		"Sitosterolemia, 210250 (3), Autosomal recessive"	Abcg5 (MGI:1351659)			
chr2	43831941	43880050	2p21	2p21		605460	"ABCG8, GBD4"	"ATP-binding cassette, subfamily G, member 8"	ABCG8	64241	ENSG00000143921		"{Gallbladder disease 4}, 611465 (3); Sitosterolemia, 210250 (3), Autosomal recessive"	Abcg8 (MGI:1914720)			
chr2	43886223	43996004	2p21	2p21		607544	"LRPPRC, LRP130, LSFC"	Leucine-rich PPR motif-containing protein	LRPPRC	10128	ENSG00000138095		"Leigh syndrome, French-Canadian type, 220111 (3), Autosomal recessive"	Lrpprc (MGI:1919666)			
chr2	44168802	44247329	2p21	2p21		603770	PPM1B	"Protein phosphatase, magnesium-dependent, 1, beta isoform"	PPM1B	5495	ENSG00000138032	formerly PP2CB		Ppm1b (MGI:101841)			
chr2	44275457	44320823	2p16.3	2p21		104614	"SLC3A1, ATR1, D2H, NBAT"	"Solute carrier family 3 (cystine, dibasic and neutral amino acid transporters), member 1"	SLC3A1	6519	ENSG00000138079		"Cystinuria, 220100 (3), Autosomal recessive, Autosomal dominant"	Slc3a1 (MGI:1195264)			
chr2	44317606	44361861	2p21	2p21		609557	"PREPL, KIAA0436, CMS22"	Prolyl endopeptidase-like	PREPL	9581	ENSG00000138078	mutation identified in 1 CMS22 patient	"?Myasthenic syndrome, congenital, 22, 616224 (3), Autosomal recessive"	Prepl (MGI:2441932)			
chr2	44361713	44772591	2p21	2p21		609559	"CAMKMT, C2orf34"	Calmodulin lysine N-methyltransferase	CAMKMT	79823	ENSG00000143919			Camkmt (MGI:1920832)			
chr2	44941897	44946076	2p21	2p21		603714	"SIX3, HPE2"	"Sine oculis homeo box, Drosophila, homolog of, 3"	SIX3	6496	ENSG00000138083		"Holoprosencephaly 2, 157170 (3), Autosomal dominant; Schizencephaly, 269160 (3)"	Six3 (MGI:102764)			
chr2	45005184	45009644	2p16-p15	2p21		604994	SIX2	"Sine oculis homeo box, Drosophila, homolog of, 2"	SIX2	10736	ENSG00000170577			Six2 (MGI:102778)			
chr2	45651314	46187989	2p21	2p21		176975	"PRKCE, PKCE"	"Protein kinase C, epsilon"	PRKCE	5581	ENSG00000171132			Prkce (MGI:97599)			
chr2	46297401	46386702	2p21-p16	2p21		603349	"EPAS1, MOP2, HIF2A, ECYT4"	Endothelial PAS domain protein 1	EPAS1	2034	ENSG00000116016		"Erythrocytosis, familial, 4, 611783 (3)"	Epas1 (MGI:109169)			
chr2	46511834	46542556	2p21	2p21		617385	"ATP6V1E2, ATP6E1"	"ATPase, H+ transporting, lysosomal, 31kD, V1 subunit E, isoform 1"	ATP6V1E2	90423	ENSG00000250565			Atp6v1e2 (MGI:1922165)			
chr2	46542408	46584687	2p21	2p21		605857	"RHOQ, ARHQ, TC10"	"Ras-homolog gene family, member Q"	RHOQ	23433	ENSG00000119729			Rhoq (MGI:1931553)			
chr2	46581273	46617111	2p21-p16	2p21		600153	PIGF	"Phosphatidylinositol glycan, class F"	PIGF	5281	ENSG00000151665	pseudogene on 5		Pigf (MGI:99462)			
chr2	46617171	46630175	2p21	2p21		604594	"CRIPT, SSMDF"	Cystine-rich PDZ binding protein	CRIPT	9419	ENSG00000119878		"Short stature with microcephaly and distinctive facies, 615789 (3), Autosomal recessive"	Cript (MGI:1929655)			
chr2	46698959	46762787	2p21	2p21		607094	"SOCS5, CIS6, KIAA0671"	Suppressor of cytokine signaling 5	SOCS5	9655	ENSG00000171150	also signals at 3p22		Socs5 (MGI:2385459)			
chr2	46901869	46941854	2p21-p16.3	2p21		607788	"MCFD2, F5F8D2"	Multiple coagulation factor deficiency protein 2	MCFD2	90411	ENSG00000180398		"Factor V and factor VIII, combined deficiency of, 613625 (3)"	Mcfd2 (MGI:2183439)			
chr2	46916128	47076135	2p21	2p21		609332	"TTC7A, TTC7, KIAA1140, MINAT, GIDID"	Tetratricopeptide repeat domain 7A	TTC7A	57217	ENSG00000068724		"Gastrointestinal defects and immunodeficiency syndrome, 243150 (3), Autosomal recessive"	Ttc7 (MGI:1920999)			
chr2	47160081	47176935	2p21	2p21		114182	"CALM2, LQT15"	Calmodulin-2	CALM2	805	ENSG00000143933		"Long QT syndrome 15, 616249 (3), Autosomal dominant"				
chr2	47369147	47387027	2p21	2p21		185535	"EPCAM, ACSTD1, TROP1, M4S1, MIC18, DIAR5, HNPCC8"	Epithelial cellular adhesion molecule	EPCAM	4072	ENSG00000119888	previously assigned to 4q	"Colorectal cancer, hereditary nonpolyposis, type 8, 613244 (3); Diarrhea 5, with tufting enteropathy, congenital, 613217 (3), Autosomal recessive"	Epcam (MGI:106653)			
chr2	47403066	47634500	2p22-p21	2p21-p16		609309	"MSH2, COCA1, FCC1, HNPCC1"	"mutS, E. coli, homolog of, 2"	MSH2	4436	ENSG00000095002		"Colorectal cancer, hereditary nonpolyposis, type 1, 120435 (3), Autosomal dominant; Mismatch repair cancer syndrome, 276300 (3), Autosomal recessive; Muir-Torre syndrome, 158320 (3), Autosomal dominant"	Msh2 (MGI:101816)			
chr2	47500000	61000000	2p16			609958	ASRT3	"Asthma-related traits, susceptibility to, 3"		100188801		max lod at rs2063871	"{Asthma-related traits, susceptibility to, 3}, 609958 (2)"				
chr2	47500000	61000000	2p16			605244	CNC2	"Carney complex, type II"	CNC2	1257			"Carney complex, type II, 605244 (2)"				
chr2	47500000	63900000	2p16-p15			604254	DYX3	"Dyslexia, susceptibility to, 3"	DYX3	11192			"{Dyslexia, susceptibility to, 3}, 604254 (2)"				
chr2	47500000	63900000	2p16-p15			611276	GLC1H	"Glaucoma 1, open angle, H"	GLC1H	399564		between D2S123 AND D2S2165	"Glaucoma 1, open angle, H, 611276 (2)"				
chr2	47500000	61000000	2p16			613549	STQTL24	Stature quantitative trait locus 24		100529223		linked to rs1520446	"{Stature QTL 24}, 613549 (2)"				
chr2	47520774	47570330	2p22-p21	2p16.3		607366	"KCNK12, THIK2"	"Potassium channel, subfamily K, member 12"	KCNK12	56660	ENSG00000184261			Kcnk12 (MGI:2684043)			
chr2	47783081	47806953	2p16	2p16.3		600678	"MSH6, GTBP, HNPCC5"	"MutS, E. coli, homolog of, 6"	MSH6	2956	ENSG00000116062	0.5 Mb from MSH2	"Colorectal cancer, hereditary nonpolyposis, type 5, 614350 (3), Autosomal dominant; Endometrial cancer, familial, 608089 (3); Mismatch repair cancer syndrome, 276300 (3), Autosomal recessive"	Msh6 (MGI:1343961)			
chr2	47806919	47905792	2p21	2p16.3		607871	"FBXO11, FBX11, VIT1, PRMT9"	F-box only protein 11	FBXO11	80204	ENSG00000138081	?2p16		Fbxo11 (MGI:2147134)			
chr2	48314639	48379294	2p22-p16	2p16.3		143089	HTLF	Human T-cell leukemia virus enhancer factor	FOXN2	3344	ENSG00000170802			Foxn2 (MGI:1347478)			
chr2	48530168	48598514	2p16.3	2p16.3		605357	"STON1, STN1, SBLF, SALF"	Stonin 1	STON1	11037	ENSG00000243244			Ston1 (MGI:1924307)			
chr2	48617779	48679608	2p16.3	2p16.3		605358	"GTF2A1L, ALF"	"General transcription factor IIA, 1-like"	GTF2A1L	11036	ENSG00000242441			Gtf2a1l (MGI:1919078)			
chr2	48686773	48755740	2p21	2p16.3		152790	"LHCGR, LHR, LCGR"	Luteinizing hormone/choriogonadotropin receptor	LHCGR	3973	ENSG00000138039		"Leydig cell adenoma, somatic, with precocious puberty, 176410 (3); Leydig cell hypoplasia with hypergonadotropic hypogonadism, 238320 (3), Autosomal recessive; Leydig cell hypoplasia with pseudohermaphroditism, 238320 (3), Autosomal recessive; Luteinizing hormone resistance, female, 238320 (3), Autosomal recessive; Precocious puberty, male, 176410 (3), Autosomal dominant"	Lhcgr (MGI:96783)			
chr2	48953160	49154526	2p21-p16	2p16.3		136435	"FSHR, ODG1"	Follicle stimulating hormone receptor	FSHR	2492	ENSG00000170820		"Ovarian dysgenesis 1, 233300 (3), Autosomal recessive; Ovarian hyperstimulation syndrome, 608115 (3), Autosomal dominant; Ovarian response to FSH stimulation, 276400 (3), Autosomal recessive"	Fshr (MGI:95583)			
chr2	49918504	51032535	2p16.3	2p16.3		600565	"NRXN1, PTHSL2, SCZD17"	Neurexin 1	NRXN1	9378	ENSG00000179915		"Pitt-Hopkins-like syndrome 2, 614325 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 17}, 614332 (3)"	Nrxn1 (MGI:1096391)			
chr2	53669979	53787008	2p16.2	2p16.2		605760	ASB3	Ankyrin repeat-containing SOCS box protein 3	ASB3	51130	ENSG00000115239			Asb3 (MGI:1929749)			
chr2	53767782	53775195	2p16.2	2p16.2		617446	CHAC2	"ChaC, E. coli, homolog of, 2"	CHAC2	494143	ENSG00000143942			Chac2 (MGI:1915294)			
chr2	53786930	53834523	2p16.2	2p16.2		611229	"ERLEC1, C2orf30"	Erlectin (endoplasmic reticulum lectin 1)	ERLEC1	27248	ENSG00000068912			Erlec1 (MGI:1914003)			
chr2	53852912	53860032	2p16	2p16.2		606704	GPR75	G protein-coupled receptor 75	GPR75	10936	ENSG00000119737			Gpr75 (MGI:2441843)			
chr2	53864066	53970839	2p16.2	2p16.2		607705	"PSME4, PA200, KIAA0077"	Proteasome activator subunit 4	PSME4	23198	ENSG00000068878			Psme4 (MGI:2143994)			
chr2	53970837	54305299	2p16.2	2p16.2		102595	"ACYP2, ACYP"	"Acylphosphatase 2, muscle type"	ACYP2	98	ENSG00000170634			Acyp2 (MGI:1922822)			
chr2	54456316	54671445	2p21	2p16.2		182790	SPTBN1	"Spectrin, beta, nonerythrocytic-1 (beta-fodrin)"	SPTBN1	6711	ENSG00000115306			Sptbn1 (MGI:98388)			
chr2	54700000	63900000	2p16.1-p15			612513	"DEL2p16.1-p15, C2DELp161-p15"	Chromosome 2p16.1-p15 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 2p16.1-p15 deletion syndrome, 612513 (4), Isolated cases"				
chr2	54700000	61000000	2p16.1			142335	HBFQTL5	Fetal hemoglobin quantitative trait locus 5	HPFH2	3247		associated with rs11886868	"[Fetal hemoglobin QTL5], 142335 (2), Autosomal dominant"				
chr2	54972188	55137830	2p14-p13	2p16.1		604475	"RTN4, NOGO"	Neurite outgrowth inhibitor (reticulon 4)	RTN4	57142	ENSG00000115310			Rtn4 (MGI:1915835)			
chr2	55231902	55235852	2p16.1	2p16.1		191343	"RPS27A, UBA80, HUBCEP80, CEP80, UBCEP1"	Ribosomal protein S27a	RPS27A	6233	ENSG00000143947			Rps27a (MGI:1925544)			
chr2	55235582	55269313	2p16-p14	2p16.1		603766	MTIF2	Mitochondrial translational initiation factor 2	MTIF2	4528	ENSG00000085760			Mtif2 (MGI:1924034)			
chr2	55287816	55419920	2p16.1	2p16.1		609736	"CCDC88A, KIAA1212, HKRP1, GIRDIN, APE, GIV, PEHOL"	Coiled-coil domain-containing protein 88A	CCDC88A	55704	ENSG00000115355	mutation identified in 1 PEHOL family	"?PEHO syndrome-like, 617507 (3), Autosomal recessive"	Ccdc88a (MGI:1925177)			
chr2	55547291	55618131	2p16.1	2p16.1		610352	"PPP4R3B, PP4R3B, SMEK2, KIAA1387"	"Protein phosphatase 4, regulatory subunit 3, beta"	PPP4R3B	57223	ENSG00000275052			Ppp4r3b (MGI:2144474)			
chr2	55634062	55693909	2p16.1	2p16.1		610316	"PNPT1, OLD35, COXPD13, DFNB70"	Polyribonucleotide nucleotidyltransferase 1	PNPT1	87178	ENSG00000138035		"Combined oxidative phosphorylation deficiency 13, 614932 (3), Autosomal recessive; Deafness, autosomal recessive 70, 614934 (3), Autosomal recessive"	Pnpt1 (MGI:1918951)			
chr2	55865961	55924162	2p16	2p16.1		601548	"EFEMP1, FBNL, DHRD"	EGF-containing fibulin-like extracellular matrix protein 1 (fibrillin-like)	EFEMP1	2202	ENSG00000115380		"Doyne honeycomb degeneration of retina, 126600 (3), Autosomal dominant"	Efemp1 (MGI:1339998)			
chr2	55982966	55983075	2p16.1	2p16.1		615096	MIR217	Micro RNA 217	MIR217	406999							
chr2	55988949	55989058	2p16.1	2p16.1		610944	"MIR216, MIRN216"	Micro RNA 216	MIR216A	406998							
chr2	57907650	58164000	2p16-p15	2p16.1		602169	VRK2	Vaccinia-related kinase-2	VRK2	7444	ENSG00000028116			Vrk2 (MGI:1917172)			
chr2	58159242	58241680	2p16.1	2p16.1		608111	"PHF9, FANCL"	PHD finger protein 9	FANCL	55120	ENSG00000115392		"Fanconi anemia, complementation group L, 614083 (3), Autosomal recessive"	Fancl (MGI:1914280)			
chr2	60451166	60553497	2p16.1	2p16.1		606557	"BCL11A, CTIP1, EVI9, KIAA1809, DILOS"	B-cell CLL/lymphoma 11A	BCL11A	53335	ENSG00000119866		"Dias-Logan syndrome, 617101 (3), Autosomal dominant"	Bcl11a (MGI:106190)			
chr2	60756229	60802085	2p16.1	2p16.1		616865	PAPOLG	"Poly(A) polymerase, gamma"	PAPOLG	64895	ENSG00000115421			Papolg (MGI:2442119)			
chr2	60881494	60928170	2p13-p12	2p16.1		164910	REL	"Oncogene REL, avian reticuloendotheliosis"	REL	5966	ENSG00000162924			Rel (MGI:97897)			
chr2	60940217	61019692	2p16.1	2p16-p15		612787	"PUS10, DOBI"	Pseudouridylate synthase 10	PUS10	150962	ENSG00000162927			Pus10 (MGI:1921717)			
chr2	61017676	61051989	2p15	2p15		601789	"PEX13, ZWS, NALD, PBD11A, PBD11B"	Peroxisome biogenesis factor 13 (peroxin 13)	PEX13	5194	ENSG00000162928		"Peroxisome biogenesis disorder 11A (Zellweger), 614883 (3), Autosomal recessive; Peroxisome biogenesis disorder 11B, 614885 (3), Autosomal recessive"	Pex13 (MGI:1919379)			
chr2	61187454	61470713	2p15	2p15		615295	"USP34, KIAA0570"	Ubiquitin-specific protease 34	USP34	9736	ENSG00000115464			Usp34 (MGI:109473)			
chr2	61477933	61538521	2p16	2p15		602559	"XPO1, CRM1"	Exportin-1 (required for chromosome region maintenance)	XPO1	7514	ENSG00000082898			Xpo1 (MGI:2144013)			
chr2	61800239	61854142	2p15	2p15		613596	"FAM161A, RP28"	"Family with sequence similarity 161, member A"	FAM161A	84140	ENSG00000170264		"Retinitis pigmentosa 28, 606068 (3)"	Fam161a (MGI:1921123)			
chr2	61868126	61888670	2p15	2p15		605142	"CCT4, CCTD, SRB"	"Chaperonin containing T-complex polypeptide 1, subunit 4"	CCT4	10575	ENSG00000115484			Cct4 (MGI:104689)			
chr2	61888722	62136069	2p16-p13	2p15		607238	"COMMD1, MURR1"	Copper metabolism Murr1 domain-containing 1	COMMD1	150684	ENSG00000173163			Commd1 (MGI:109474)			
chr2	62196126	62224730	2p15	2p15		605581	"B3GNT2, B3GNT1, B3GNT"	"Beta-1,3-N-acetylglucosyaminyltransferase 2"	B3GNT2	10678	ENSG00000170340			B3gnt2 (MGI:1889505)			
chr2	62452777	62511893	2p15	2p15		614950	TMEM17	Transmembrane protein 17	TMEM17	200728	ENSG00000186889			Tmem17 (MGI:2144205)			
chr2	62673850	63046486	2p15	2p15		609922	"EHBP1, KIAA0903, HPC12"	EH domain-binding protein 1	EHBP1	23301	ENSG00000115504		"{Prostate cancer, hereditary, 12}, 611868 (3)"	Ehbp1 (MGI:2667252)			
chr2	63050056	63057830	2p13	2p15		600036	OTX1	"Orthodenticle, Drosophila, homolog of, 1"	OTX1	5013	ENSG00000115507			Otx1 (MGI:97450)			
chr2	63119558	63588798	2p15	2p15		613580	"WDPCP, C2orf86, BBS15, CHDTHP"	WD repeat-containing planar cell polarity effector	WDPCP	51057	ENSG00000143951	mutation identified in 1 BBS15 family and 1 CHDTHP patient	"?Bardet-Biedl syndrome 15, 615992 (3), Autosomal recessive; ?Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085 (3), Autosomal recessive"	Wdpcp (MGI:2144467)			
chr2	63588608	63607196	2p16	2p15		154200	MDH1	"Malate dehydrogenase, soluble"	MDH1	4190	ENSG00000014641	proximal to APOB		Mdh1 (MGI:97051)			
chr2	63840963	63891561	2p14-p13	2p15		191760	"UGP2, UGPP2"	Uridyl diphosphate glucose pyrophosphorylase-2	UGP2	7360	ENSG00000169764			Ugp2 (MGI:2183447)			
chr2	63892148	64019421	2p14	2p15-p14		614633	"VPS54, VPS54L, WR"	"Vacuolar protein sorting 54, S. Cerevisiae, homolog of"	VPS54	51542	ENSG00000143952			Vps54 (MGI:2178798)			
chr2	63900000	71300000	2p14-p13.3			610071	HRPT3	Hyperparathyroidism 3		780919		between D2S2368 and D2S358	"Hyperparathyroidism 3, 610071 (2)"				
chr2	63900000	74800000	2p14-p13			612853	RLS7	"Restless legs syndrome, susceptibility to, 7"		100302561		associated with rs2300478	"{Restless legs syndrome 7}, 612853 (2)"				
chr2	64092651	64144470	2p13.3	2p14		614797	PELI1	"Pellino, Drosophila, homolog of, 1"	PELI1	57162	ENSG00000197329			Peli1 (MGI:1914495)			
chr2	64454192	64461382	2p14	2p14		617902	LGALSL	Galectin-like protein	LGALSL	29094	ENSG00000119862						
chr2	64631620	64751085	2p14	2p14		617851	"SERTAD2, TRIPBR2, KIAA0127"	SERTA domain-containing protein 2	SERTAD2	9792	ENSG00000179833			Sertad2 (MGI:1931026)			
chr2	64988444	65023864	2p14	2p14		600229	"SLC1A4, SATT, ASCT1, SPATCCM"	"Solute carrier family 1 (glutamate/neutral amino acid transporter), member 4"	SLC1A4	6509	ENSG00000115902		"Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 (3), Autosomal recessive"	Slc1a4 (MGI:2135601)			
chr2	65056360	65087007	2p14	2p14		616889	"CEP68, KIAA0582"	"Centrosomal protein, 68kD"	CEP68	23177	ENSG00000011523			Cep68 (MGI:2667663)			
chr2	65086853	65130300	2p14	2p14		179508	"RAB1, RAB1A"	"RAB1, member RAS oncogene family"	RAB1A	5861	ENSG00000138069			Rab1a (MGI:97842)			
chr2	65227694	65271252	2p14	2p14		604221	"ACTR2, ARP2"	Actin-related protein 2	ACTR2	10097	ENSG00000138071			Actr2 (MGI:1913963)			
chr2	65307424	65432521	2p14	2p14		609292	SPRED2	Sprouty-related EVH1 domain-containing protein 2	SPRED2	200734	ENSG00000198369			Spred2 (MGI:2150019)			
chr2	66435399	66572758	2p14-p13	2p14		601739	MEIS1	"Meis1, mouse, homolog of"	MEIS1	4211	ENSG00000143995						
chr2	67397309	67410410	2p15-p13	2p14		613196	"ETAA1, ETAA16"	Ewing tumor-associated antigen 1	ETAA1	54465	ENSG00000143971			Etaa1 (MGI:1915395)			
chr2	68042199	68063026	2p13-p12	2p14		606997	"C1D, SUNCOR"	Nuclear DNA-binding protein C1D	C1D	10438	ENSG00000197223	pseudogene on chr.10		C1d (MGI:1927354)			
chr2	68130148	68157559	2q14	2p14		610729	"WDR92, LOC116143, MONAD"	WD repeat-containing protein 92	WDR92	116143	ENSG00000243667			Wdr92 (MGI:2144224)			
chr2	68178856	68252518	2p16-p15	2p14		601302	"PPP3R1, CALNB1"	"Protein phosphatase-3 (formerly 2B), regulatory subunit B (19kD), alpha isoform (calcineurin B, type I)"	PPP3R1	5534	ENSG00000221823			Ppp3r1 (MGI:107172)			
chr2	68365189	68397452	2p	2p14		173570	PLEK	Pleckstrin	PLEK	5341	ENSG00000115956			Plek (MGI:1860485)			
chr2	68400000	74800000	2p13			602966	OFC2	Orofacial cleft-2	OFC2	4964		?relation to TGFA	"Orofacial cleft-2, 602966 (2)"				
chr2	68400000	74800000	2p13			602404	PARK3	Parkinson disease 3	PARK3	5072			"{Parkinson disease 3}, 602404 (2)"				
chr2	68400000	74800000	2p13			189800	"PEE1, PREG1"	Preeclampsia/eclampsia 1	PEE1	5177		?distinct loci at 2p25 and 9p13	"Preeclampsia/eclampsia 1, 189800 (2), Autosomal dominant"				
chr2	68467558	68580161	2p14	2p13.3		611035	"AFPL, C2orf13"	Aprataxin- and PNK-like factor	APLF	200558	ENSG00000169621			Aplf (MGI:1919353)			
chr2	68643587	68655575	2p13.3	2p13.3		607122	"PROKR1, PKR1, GPR73"	Prokineticin receptor 1	PROKR1	10887	ENSG00000169621			Prokr1 (MGI:1929676)			
chr2	68710509	68826844	2p13	2p13.3		610587	"ARHGAP25, KAIA0053"	RHO GTPase-activating protein 25	ARHGAP25	9938	ENSG00000163219			Arhgap25 (MGI:2443687)			
chr2	68860915	68871516	2p13.3	2p13.3		608748	BMP10	Bone morphogenetic protein 10	BMP10	27302	ENSG00000163217			Bmp10 (MGI:1338820)			
chr2	68974572	68980979	2p13.3	2p13.3		606402	"GKN1, CA11"	Gastrokine 1	GKN1	56287	ENSG00000169605			Gkn1 (MGI:1913533)			
chr2	69013143	69249326	2p13.1	2p13.3		606410	"ANTXR1, TEM8, ATR, GAPO"	Anthrax toxin receptor 1	ANTXR1	84168	ENSG00000169604	mutation identified in 1 HCI patient	"GAPO syndrome, 230740 (3), Autosomal recessive; {?Hemangioma, capillary infantile, susceptibility to}, 602089 (3), Autosomal dominant"	Antxr1 (MGI:1916788)			
chr2	69319768	69387253	2p13	2p13.3		138292	"GFPT1, GFAT1, GFPT1L, MSLG, CMS12, CMSTA1"	Glutamine-fructose-6-phosphate transaminase	GFPT1	2673	ENSG00000198380		"Myasthenia, congenital, 12, with tubular aggregates, 610542 (3), Autosomal recessive"	Gfpt1 (MGI:95698)			
chr2	69396112	69439648	2p15-p13	2p13.3		608100	"NFU1, HIRIP, MMDS1"	"NFU1 iron-sulfur cluster scaffold, S. cerevisiae, homolog of"	NFU1	27247	ENSG00000169599		"Multiple mitochondrial dysfunctions syndrome 1, 605711 (3), Autosomal recessive"	Nfu1 (MGI:1913290)			
chr2	69457994	69643844	2p13.3	2p13.3		616405	"AAK1, KIAA1048"	Adaptor protein 2-associated kinase 1	AAK1	22848	ENSG00000115977			Aak1 (MGI:1098687)			
chr2	69643804	69826476	2p13	2p13.3		106491	"ANXA4, ANX4"	Annexin A4 (placental anticoagulant protein II)	ANXA4	307	ENSG00000196975			Anxa4 (MGI:88030)			
chr2	69915040	69942944	2p13	2p13.3		600021	MAD	MAD protein (MAX-binding protein)	MXD1	4084	ENSG00000059728			Mxd1 (MGI:96908)			
chr2	69960088	69962264	2p13.1	2p13.3		611765	"ASPRV1, SASP, TAPS, MUNO"	"Aspartic peptidase, retroviral-like 1"	ASPRV1	151516	ENSG00000244617			Asprv1 (MGI:1915105)			
chr2	70087452	70089202	2p13-p12	2p13.3		601209	PCBP1	Poly(rC)-binding protein-1	PCBP1	5093	ENSG00000169564			Pcbp1 (MGI:1345635)			
chr2	70209443	70248792	2p13	2p13.3		603518	"TIA1, WDM"	TIA1 cytotoxic granule-associated RNA-binding protein	TIA1	7072	ENSG00000116001		"Welander distal myopathy, 604454 (3), Autosomal recessive, Autosomal dominant"	Tia1 (MGI:107914)			
chr2	70258098	70281184	2p13.3	2p13.3		610995	"PCYOX1, PCL1, KIAA0908"	Prenylcysteine oxidase 1	PCYOX1	51449	ENSG00000116005			Pcyox1 (MGI:1914131)			
chr2	70281361	70293770	2p13.3	2p13.3		603542	SNRPG	Small nuclear ribonucleoprotein polypeptide G	SNRPG	6637	ENSG00000143977						
chr2	70295975	70302087	2p13.3	2p13.3		616275	FAM136A	"Family with sequence similarity 136, member A"	FAM136A	84908	ENSG00000035141			Fam136a (MGI:1913738)			
chr2	70447279	70554014	2p13	2p13.3		190170	TGFA	"Transforming growth factor, alpha"	TGFA	7039	ENSG00000163235			Tgfa (MGI:98724)			
chr2	70656783	70768242	2p14-p13	2p13.3		102681	ADD2	"Adducin-2, beta"	ADD2	119	ENSG00000075340			Add2 (MGI:87919)			
chr2	70777309	70790642	2p12	2p13.3		608697	"FIGLA, POF6"	"Factor in germline alpha, mouse, homolog of"	FIGLA	344018	ENSG00000183733		"Premature ovarian failure 6, 612310 (3), Autosomal dominant"	Figla (MGI:1349421)			
chr2	70825247	70860786	2p13	2p13.3		604862	"CD207, LANGERIN, CLEC4K"	CD207 antigen	CD207	50489	ENSG00000116031	mutation identified in 1 patient	"[?Birbeck granule deficiency], 613393 (3)"	Cd207 (MGI:2180021)			
chr2	70900550	70933916	2p13	2p13.3		604295	VAX2	Ventral anterior homeo box 2	VAX2	25806	ENSG00000116035			Vax2 (MGI:1346018)			
chr2	70935867	70965430	2cen-q13	2p13.3		192132	"ATP6B1, VPP3"	"ATPase, H+ transporting, lysosomal, beta polypeptide, 58kD (vacuolar proton pump, subunit 3)"	ATP6V1B1	525	ENSG00000116039		"Renal tubular acidosis with deafness, 267300 (3), Autosomal recessive"	Atp6v1b1 (MGI:103285)			
chr2	70977182	70986676	2p13.3	2p13.3		617009	ANKRD53	Ankyrin repeat domain-containing protein 53	ANKRD53	79998	ENSG00000144031			Ankrd53 (MGI:1922555)			
chr2	71068277	71078867	2p13.3	2p13.3		606828	"NAGK, GNK"	N-acetylglucosamine kinase	NAGK	55577	ENSG00000124357			Nagk (MGI:1860418)			
chr2	71109675	71130287	2p13.3	2p13.3		608419	MCEE	Methylmalonyl-CoA epimerase	MCEE	84693	ENSG00000124370		"Methylmalonyl-CoA epimerase deficiency, 251120 (3), Autosomal recessive"	Mcee (MGI:1920974)			
chr2	71182737	71227109	2p13.3	2p13.3		611018	PAIP2B	Polyadenylate-binding protein-interacting protein 2B	PAIP2B	400961	ENSG00000124374			Paip2b (MGI:2386865)			
chr2	71276592	71435060	2p13.2	2p13.3-p13.2		614349	"ZNF638, NP220"	Zinc finger protein 638	ZNF638	27332	ENSG00000075292			Zfp638 (MGI:1203484)			
chr2	71453153	71686762	2p13.3-p13.1	2p13.2		603009	"DYSF, LGMD2B, MMD1"	Dysferlin	DYSF	8291	ENSG00000135636		"Miyoshi muscular dystrophy 1, 254130 (3), Autosomal recessive; Muscular dystrophy, limb-girdle, type 2B, 253601 (3), Autosomal recessive; Myopathy, distal, with anterior tibial onset, 606768 (3), Autosomal recessive"	Dysf (MGI:1349385)			
chr2	72129237	72147861	2p13.2	2p13.2		605207	"CYP26B1, CYP26A2, P450RAI2, RHFCA"	"Cytochrome P450, subfamily XXVIB, polypeptide 1"	CYP26B1	56603	ENSG00000003137		"Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies, 614416 (3)"	Cyp26b1 (MGI:2176159)			
chr2	72175983	72826041	2p13.2	2p13.2		607880	"EXOC6B, SEC15B, KIAA0919"	Exocyst complex component 6B	EXOC6B	23233	ENSG00000144036			Exoc6b (MGI:1923164)			
chr2	72887382	72892159	2p14-p12	2p13.2		182125	SPR	Sepiapterin reductase	SPR	6697	ENSG00000116096		"Dystonia, dopa-responsive, due to sepiapterin reductase deficiency, 612716 (3), ?Autosomal dominant, Autosomal recessive"	Spr (MGI:103078)			
chr2	72910948	72936690	2p14-p13	2p13.2		600034	EMX1	"Empty spiracles, Drosophila, homolog of, 1"	EMX1	2016	ENSG00000135638	close to VAX2		Emx1 (MGI:95387)			
chr2	72942035	73071835	2p13	2p13.2		615572	SFXN5	Sideroflexin 5	SFXN5	94097	ENSG00000144040			Sfxn5 (MGI:2137681)			
chr2	73073381	73113017	2p13-p12	2p13.2		605536	"RAB11RIP5, RIP11, KIAA0857"	Rab11 family-interacting protein 5	RAB11FIP5	26056	ENSG00000135631			Rab11fip5 (MGI:1098586)			
chr2	73233424	73253021	2p13	2p13.2		605140	CCT7	"Chaperonin containing T-complex polypeptide 1, subunit 7"	CCT7	10574	ENSG00000135624			Cct7 (MGI:107184)			
chr2	73254681	73284448	2p13.2	2p13.2		609108	"FBXO41, FBX41, KIAA1940"	F-box only protein 41	FBXO41	150726	ENSG00000163013			Fbxo41 (MGI:1261912)			
chr2	73290928	73293700	2p13	2p13.2		128992	"EGR4, NGFIC"	Early growth response-4	EGR4	1961	ENSG00000135625			Egr4 (MGI:99252)			
chr2	73385757	73609918	2p13	2p13.1		606844	"ALMS1, ALSS, KIAA0328"	Alstrom syndrome gene	ALMS1	7840	ENSG00000116127		"Alstrom syndrome, 203800 (3), Autosomal recessive"	Alms1 (MGI:1934606)			
chr2	73640722	73642409	2p13.1-p12	2p13.1		606716	"NAT8, TSC510"	N-acetyltransferase 8	NAT8	9027	ENSG00000144035			Nat8 (MGI:1915646)			
chr2	73700508	73701339	2p13.1-p12	2p13.1		608190	"NAT8B, CML2"	N-acetyltransferase 8B	NAT8B	51471	ENSG00000204872			Nat8f1 (MGI:1913366)			
chr2	73729836	73737405	2p13.1	2p13.1		608680	"TPRKB, GAMOS5"	TP53RK-binding protein	TPRKB	51002	ENSG00000144034		"Galloway-Mowat syndrome 5, 617731 (3), Autosomal recessive"	Tprkb (MGI:1917036)			
chr2	73762197	73780156	2p13.1	2p13.1		603092	"DUSP11, PIR1"	"Dual specificity phosphatase-11, RNA/RNP complex-interacting"	DUSP11	8446	ENSG00000144048			Dusp11 (MGI:1919352)			
chr2	73828910	73873660	2p13.1	2p13.1		606247	"STAMBP, AMSH, MICCAP"	STAM binding protein	STAMBP	10617	ENSG00000124356		"Microcephaly-capillary malformation syndrome, 614261 (3), Autosomal recessive"	Stambp (MGI:1917777)			
chr2	73892965	73919652	2p13.1	2p13.1		102545	"ACTG2, ACTA3, VSCM"	"Actin, gamma-2, smooth muscle, enteric"	ACTG2	72	ENSG00000163017		"Visceral myopathy, 155310 (3), Autosomal dominant"	Actg2 (MGI:104589)			
chr2	73926825	73958960	2p13	2p13.1		601465	"DGUOK, DGK, MTDPS3, PEOB4, NCPH"	"Deoxyguanosine kinase, mitochondrial"	DGUOK	1716	ENSG00000114956		"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 (3), Autosomal recessive; Portal hypertension, noncirrhotic, 617068 (3), Autosomal recessive; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4, 617070 (3), Autosomal recessive"	Dguok (MGI:1351602)			
chr2	73982035	74135393	2p13.1	2p13.1		613555	"TET3, KIAA0401"	"TET oncogene family, member 3"	TET3	200424	ENSG00000187605			Tet3 (MGI:2446229)			
chr2	74135400	74147911	2p13.1	2p13.1		613183	"BOLA3, MMDS2"	"BolA, E. coli, homolog of, 3"	BOLA3	388962	ENSG00000163170		"Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia, 614299 (3), Autosomal recessive"	Bola3 (MGI:1925903)			
chr2	74216241	74343406	2p13	2p13.1		606757	"SLC4A5, NBC4"	"Solute carrier family 4, sodium bicarbonate cotransporter, member 5"	SLC4A5	57835	ENSG00000188687			Slc4a5 (MGI:2443220)			
chr2	74361153	74392086	2p13	2p13.1		601143	"DCTN1, HMN7B"	"Dynactin 1 (p150, glued, Drosophila, homolog of)"	DCTN1	1639	ENSG00000204843		"{Amyotrophic lateral sclerosis, susceptibility to}, 105400 (3), Autosomal recessive, Autosomal dominant; Neuropathy, distal hereditary motor, type VIIB, 607641 (3), Autosomal dominant; Perry syndrome, 168605 (3), Autosomal dominant"	Dctn1 (MGI:107745)			
chr2	74425860	74441932	2p13	2p13.1		602288	RTKN	Rhotekin	RTKN	6242	ENSG00000114993			Rtkn (MGI:107371)			
chr2	74455022	74457959	2p13	2p13.1		616456	"INO80B, PAPA1, HMGA1L4"	"INO80 complex, subunit B"	INO80B	83444	ENSG00000115274			Ino80b (MGI:1917270)			
chr2	74458399	74460890	2p12	2p13.1		606961	WBP1	WW domain-binding protein 1	WBP1	23559	ENSG00000239779			Wbp1 (MGI:104710)			
chr2	74461056	74465409	2p13.1	2p13.1		601336	"MOGS, GCS1, CDG2B"	Mannosyl-oligosaccharide glucosidase	MOGS	7841	ENSG00000115275		"Congenital disorder of glycosylation, type IIb, 606056 (3), Autosomal recessive"	Mogs (MGI:1929872)			
chr2	74471957	74472814	2p12	2p13.1		611857	MRPL53	Mitochondrial ribosomal protein L53	MRPL53	116540	ENSG00000204822	pseudogene on 1		Mrpl53 (MGI:1915749)			
chr2	74497516	74503315	2p13	2p13.1		607164	LBX2	Lady bird-like homeo box 2	LBX2	85474	ENSG00000179528			Lbx2 (MGI:1342288)			
chr2	74514468	74517147	2p13.1-p12	2p13.1		604240	"TLX2, HOX11L1"	"T-cell leukemia, homeobox 2"	TLX2	3196	ENSG00000115297			Tlx2 (MGI:1350935)			
chr2	74526647	74529896	2p13	2p13.1		602434	AUP1	Ancient ubiquitous protein 1	AUP1	550	ENSG00000115307			Aup1 (MGI:107789)			
chr2	74529404	74533555	2p12	2p13.1		606441	"HTRA2, OMI, PARK13, PRSS25, MGCA8"	HTRA serine peptidase 2	HTRA2	27429	ENSG00000115317		"3-methylglutaconic aciduria, type VIII, 617248 (3), Autosomal recessive; {Parkinson disease 13}, 610297 (3)"	Htra2 (MGI:1928676)			
chr2	74532257	74555718	2p13.3	2p13.1		607163	LOXL3	Lysyl oxidase-like 3	LOXL3	84695	ENSG00000115318			Loxl3 (MGI:1337004)			
chr2	74549019	74557550	2p13	2p13.1		602919	DOK1	Downstream of tyrosine kinase 1	DOK1	1796	ENSG00000115325			Dok1 (MGI:893587)			
chr2	74654227	74699012	2p13	2p13.1		603706	SEMAW	Semaphorin W	SEMA4F	10505	ENSG00000135622			Sema4f (MGI:1340055)			
chr2	74800000	83100000	2p12			607304	"CTRCT27, CCNP"	"Cataract 27, nuclear progressive"		266979		near D2S2333	"Cataract 27, nuclear progressive, 607304 (2)"				
chr2	74800000	91800000	2p12-p11.2			613564	"DEL2p12p11.2, C2DELp12p11.2"	Chromosome 2p12-p11.2 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 2p12-p11.2 deletion syndrome, 613564 (4)"				
chr2	74800000	83100000	2p12			608394	DFNA43	"Deafness, autosomal dominant 43"	DFNA43	192676		max lod at D2S139	"Deafness, autosomal dominant 43, 608394 (2), Autosomal dominant"				
chr2	74800000	147900000	2p12-q22			139900	HSR	"Hand skill, relative"		338386			"[Handedness], 139900 (2), Autosomal dominant"				
chr2	74800000	83100000	2p12			146970	IGKJ@	Immunoglobulin kappa light chain joining gene cluster		7842		5 genes					
chr2	74800000	83100000	2p12			146980	IGKV@	Immunoglobulin kappa light chain variable gene cluster		3519		25+ genes in 4 classes; orphon gene 1.5Mb telomeric of IGKC					
chr2	74832654	74893353	2p12	2p12		601125	HK2	"Hexokinase-2, muscle"	HK2	3099	ENSG00000159399	no recombination with TGFA		Hk2 (MGI:1315197)			
chr2	74958642	74969731	2p12	2p12		607269	POLE4	"Polymerase, DNA, epsilon-4"	POLE4	56655	ENSG00000115350			Pole4 (MGI:1914229)			
chr2	75046462	75199518	2p11	2p12		162323	"TACR1, TAC1R, NK1R"	Tachykinin receptor 1 (substance P receptor; neurokinin-1 receptor)	TACR1	6869	ENSG00000115353			Tacr1 (MGI:98475)			
chr2	75646782	75662207	2p11.2-q11.2	2p12		611832	"MRPL19, MRPL15, KIAA0104"	Mitochondrial ribosomal protein L19	MRPL19	9801	ENSG00000115364			Mrpl19 (MGI:1926274)			
chr2	75655605	75711641	2p11.2-p11.1	2p12		189901	"C2orf3, TCF9, GCF"	GC factor	GCFC2	6936	ENSG00000005436			Gcfc2 (MGI:2141656)			
chr2	76747722	77522432	2p12	2p12		610870	LRRTM4	Leucine-rich repeat transmembrane protein 4	LRRTM4	80059	ENSG00000176204			Lrrtm4 (MGI:2389180)			
chr2	79025663	79028503	2p12	2p12		609933	"REG3G, PAP1B"	Regenerating islet-derived 3-gamma	REG3G	130120	ENSG00000143954			Reg3g (MGI:109406)			
chr2	79085022	79088023	2p12	2p12		167771	"REGL, PSPS2"	"Regenerating islet-derived, rat, homolog-like (pancreatic stone protein-like; pancreatic thread protein-like)"	REG1B	5968	ENSG00000172023			Reg2 (MGI:97896)			
chr2	79120457	79123418	2p12	2p12		167770	"REG1A, PSPS1, REG"	"Regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein)"	REG1A	5967	ENSG00000115386			Reg1 (MGI:97895)			
chr2	79157005	79159753	2p12	2p12		167805	PAP	Pancreatitis-associated protein	REG3A	5068	ENSG00000172016			Reg3b (MGI:97478)			
chr2	79505053	80648867	2p12-p11.1	2p12		114025	"CTNNA2, CAPR, CTNR"	"Catenin, alpha-2 (cadherin-associated protein, related)"	CTNNA2	1496	ENSG00000066032			Ctnna2 (MGI:88275)			
chr2	80301877	80304427	2p12	2p12		610867	LRRTM1	Leucine-rich repeat transmembrane protein 1	LRRTM1	347730	ENSG00000162951			Lrrtm1 (MGI:2389173)			
chr2	84423522	84459461	2p11.2	2p11.2		611224	"SUCLG1, SUCLA1, MTDPS9"	"Succinate-CoA ligase, alpha subunit"	SUCLG1	8802	ENSG00000163541		"Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria), 245400 (3), Autosomal recessive"	Suclg1 (MGI:1927234)			
chr2	84459571	84819588	2p11.2	2p11.2		603336	"DNAH6, HL2"	"Dynein, axonemal, heavy chain 6"	DNAH6	1768	ENSG00000115423			Dnah6 (MGI:107744)			
chr2	84821649	84881974	2p11.2	2p11.2		614912	"TRABD2A, TIKI1"	TRAB domain-containing protein 2A	TRABD2A	129293	ENSG00000186854						
chr2	84905638	84906674	2p11.2	2p11.2		188399	TMSB10	"Thymosin, beta-10"	TMSB10	9168	ENSG00000034510						
chr2	84971107	85059471	2p11.2	2p11.2		614719	"KCMF1, DEBT91, FIGC"	Potassium channel modulatory factor 1	KCMF1	56888	ENSG00000176407			Kcmf1 (MGI:1921537)			
chr2	85133459	85310387	2p11.2	2p11.2		604652	TCF7L1	Transcription factor 7-like 1	TCF7L1	83439	ENSG00000152284			Tcf7l1 (MGI:1202876)			
chr2	85318017	85328295	2p11.2	2p11.2		603062	"TGOLN2, TGN46, TGN38"	"Trans-golgi network protein 2, 46kD"	TGOLN2	10618	ENSG00000152291						
chr2	85341954	85354697	2p11.2	2p11.2		617597	RETSAT	Retinol saturase	RETSAT	54884	ENSG00000042445			Retsat (MGI:1914692)			
chr2	85354393	85391751	2p11.3	2p11.2		615427	"ELMOD3, RBED1, DFNB88"	ELMO/CED12 domain-containing protein 3	ELMOD3	84173	ENSG00000115459	one family identified with mutation	"?Deafness, autosomal recessive 88, 615429 (3), Autosomal recessive"	Elmod3 (MGI:2445168)			
chr2	85394747	85418466	2cen-q24	2p11.2		153615	CAPG	"Capping protein (actin filament), gelsolin-like"	CAPG	822	ENSG00000042493			Capg (MGI:1098259)			
chr2	85537466	85538885	2p11.2	2p11.2		616350	PARTICL	Promoter of MAT2A antisense radiation-induced circulating long noncoding RNA	PARTICL	100630918		overlaps promoter of MAT2A on opposite strand					
chr2	85538977	85545279	2p11.2	2p11.2		601468	"MAT2A, MATA2, SAMS2"	"Methionine adenosyltransferase II, alpha"	MAT2A	4144	ENSG00000168906			Mat2a (MGI:2443731)			
chr2	85544719	85561533	2p12	2p11.2		137167	"GGCX, VKCFD1"	Gamma-glutamyl carboxylase	GGCX	2677	ENSG00000115486		"Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency, 610842 (3); Vitamin K-dependent clotting factors, combined deficiency of, 1, 277450 (3), Autosomal recessive"	Ggcx (MGI:1927655)			
chr2	85577490	85582032	2p12-p11.2	2p11.2		603177	VAMP8	Vesicle-associated membrane protein 8	VAMP8	8673	ENSG00000118640			Vamp8 (MGI:1336882)			
chr2	85584407	85593387	2p11.2	2p11.2		607029	VAMP5	Vesicle-associated membrane protein 5 (myobrevin)	VAMP5	10791	ENSG00000168899			Vamp5 (MGI:1858622)			
chr2	85593822	85597707	2p11.2	2p11.2		612490	RNF181	Ring finger protein 181	RNF181	51255	ENSG00000168894			Rnf181 (MGI:1913760)			
chr2	85598546	85602698	2p11.2	2p11.2		616757	"TMEM150A, TMEM150"	Transmembrane protein 150A	TMEM150A	129303	ENSG00000168890			Tmem150a (MGI:2385244)			
chr2	85602841	85649283	2p11.2	2p11.2		611594	"USP39, SAD1"	Ubiquitin-specific protease 39	USP39	10713	ENSG00000168883			Usp39 (MGI:107622)			
chr2	85657316	85668740	2p12-p11.2	2p11.2		178640	"SFTPB, SFTB3, SMDP1"	"Pulmonary surfactant-associated protein B, 18kD"	SFTPB	6439	ENSG00000168878		"Surfactant metabolism dysfunction, pulmonary, 1, 265120 (3), Autosomal recessive"	Sftpb (MGI:109516)			
chr2	85694290	85698853	2p12-q11	2p11.2		188855	"GNLY, D2S69E, TLA519"	Granulysin (T-lymphocyte activation gene 519)	GNLY	10578	ENSG00000115523						
chr2	85839132	85889033	2p11.2	2p11.2		604402	"SIAT9, ST3GALV, SPDRS"	Sialyltransferase 9	ST3GAL5	8869	ENSG00000115525		"Salt and pepper developmental regression syndrome, 609056 (3), Autosomal recessive"	St3gal5 (MGI:1339963)			
chr2	86020215	86106154	2p11.2	2p11.2		616404	"POLR1A, RPA194, AFDCIN"	"Polymerase I, RNA, subunit A"	POLR1A	25885	ENSG00000068654		"Acrofacial dysostosis, Cincinnati type, 616462 (3), Autosomal dominant"	Polr1a (MGI:1096397)			
chr2	86106181	86142156	2p11.2	2p11.2		614918	PTCD3	Pentatricopeptide repeat domain-containing protein 3	PTCD3	55037	ENSG00000132300			Ptcd3 (MGI:1917206)			
chr2	86143931	86195769	2p11.2	2p11.2		600378	"IMMT, HMP"	"Inner membrane protein, mitochondrial (mitofilin)"	IMMT	10989	ENSG00000132305	pseudogene on chr.21		Immt (MGI:1923864)			
chr2	86199432	86213797	2p11.2	2p11.2		611841	MRPL35	Mitochondrial ribosomal protein L35	MRPL35	51318	ENSG00000132313	"pseudogenes on 6, 10, and X"		Mrpl35 (MGI:1913473)			
chr2	86213992	86338082	2p11.2	2p11.2		609139	"REEP1, C2orf23, SPG31, HMN5B"	Receptor expression-enhancing protein 1	REEP1	65055	ENSG00000068615	mutation identified in 1 HMN5B family	"?Neuronopathy, distal hereditary motor, type VB, 614751 (3), Autosomal dominant; Spastic paraplegia 31, autosomal dominant, 610250 (3), Autosomal dominant"	Reep1 (MGI:1098827)			
chr2	86440646	86492715	2p11.2	2p11.2		611512	"KDM3A, JMJD1A, JHDM2A, TSGA, KIAA0742"	Lysine-specific demethylase 3A	KDM3A	55818	ENSG00000115548			Kdm3a (MGI:98847)			
chr2	86503429	86563496	2p24	2p11.2		610052	"VPS24, CHMP3, NEDF"	"Vacuolar protein sorting 24, yeast, homolog of"	CHMP3	51652	ENSG00000115561			Chmp3 (MGI:1913950)			
chr2	86603392	86623876	2p11.2	2p11.2		602507	"ZFP103, KF1"	"Zinc finger protein 103, mouse, homolog of"	RNF103	7844	ENSG00000239305			Rnf103 (MGI:109483)			
chr2	86784604	86808395	2p12	2p11.2		186910	CD8A	"CD8 antigen, alpha polypeptide  (p32)"	CD8A	925	ENSG00000153563	distal to IGK	"CD8 deficiency, familial, 608957 (3), Autosomal recessive"	Cd8a (MGI:88346)			
chr2	86815336	86861923	2p12	2p11.2		186730	"CD8B1, CD8B"	"CD8 antigen, beta polypeptide 1 (p37)"	CD8B	926	ENSG00000172116	"pseudogene, CD8B2, on 2q12"		Cd8b1 (MGI:88347)			
chr2	86913576	87013975	2p11.2	2p11.2		612704	"RGPD1, RGP1"	RANBP2-like and GRIP domain-containing protein 1	RGPD1	400966	ENSG00000187627			Ranbp2 (MGI:894323)			
chr2	87010463	87021845	2p11-q11	2p11.2		173340	"PLGLB1, PLGL, PRGB"	Plasminogen-like B1	PLGLB1	5343	ENSG00000183281						
chr2	87757197	87992818	2p11.2	2p11.2		612705	"RGPD2, RGP2"	RANBP2-like and GRIP domain-containing protein 2	RGPD2	729857	ENSG00000185304			Ranbp2 (MGI:894323)			
chr2	88067779	88113383	2p11.2	2p11.2		606846	"SMYD1, BOP, ZMYND18"	SET and MYND domain-containing protein 1	SMYD1	150572	ENSG00000115593			Smyd1 (MGI:104790)			
chr2	88122981	88128130	2p11	2p11.2		134650	FABP1	"Fatty acid-binding protein, liver"	FABP1	2168	ENSG00000163586			Fabp1 (MGI:95479)			
chr2	88170294	88186636	2p11.2	2p11.2		611261	"THNSL2, THS2"	Threonine synthase-like 2	THNSL2	55258	ENSG00000144115			Thnsl2 (MGI:3041254)			
chr2	88446786	88452534	2p11.2	2p11.2		612351	FOXI3	Forkhead box I3	FOXI3	344167	ENSG00000214336			Foxi3 (MGI:3511278)			
chr2	88556739	88627575	2p12	2p11.2		604032	"EIF2AK3, PEK, PERK, WRS"	Eukaryotic translation initiation factor 2-alpha kinase 3	EIF2AK3	9451	ENSG00000172071		"Wolcott-Rallison syndrome, 226980 (3), Autosomal recessive"	Eif2ak3 (MGI:1341830)			
chr2	88691657	88750934	2p11.2	2p11.2		180430	"RPIA, RPI, RPIAD"	Ribose 5-phosphate isomerase A	RPIA	22934	ENSG00000153574	mutation identified in 1 RPAID patient	"?Ribose 5-phosphate isomerase deficiency, 608611 (3), Autosomal recessive"	Rpia (MGI:103254)			
chr2	88832221	88833330	2p12	2p11.2		146780	IGKDEL	Immunoglobulin kappa polypeptide deleting element	IGKDEL	3515							
chr2	88857360	88857682	2p12	2p11.2		147200	"IGKC, IGKCD"	Immunoglobulin kappa constant region	IGKC	3514			"Kappa light chain deficiency, 614102 (3), Autosomal recessive"				
chr2	93900000	242193529	2q			606053	AUTS5	"Autism, susceptibility to, 5"		94313		max lod at D2S188	"{Autism susceptibility 5}, 606053 (2), Autosomal recessive, Autosomal dominant"				
chr2	93900000	108700000	2q11-q12			612006	CELIAC8	"Celiac disease, susceptibility to, 8"		100188870		associated with rs917997 and rs13015714	"{Celiac disease, susceptibility to, 8}, 612006 (2)"				
chr2	93900000	242193529	2q			606963	COPD	"Pulmonary disease, chronic obstructive, severe early-onset"		260431		?SERPINE2	"Pulmonary disease, chronic obstructive, severe early-onset, 606963 (2)"				
chr2	93900000	112200000	2cen-q13			606689	GLC1B	"Glaucoma 1, open angle, B (adult-onset)"	GLC1B	2722			"Glaucoma 1B, primary open angle, adult onset, 606689 (2)"				
chr2	93900000	129100000	2q11-q14			611897	NNO3	Nanophthalmos 3		100187717		max lod at D2S2265	"Nanophthalmos 3, 611897 (2)"				
chr2	95025654	95053991	2cen-q13	2q11.1		188860	MAL	T-lymphocyte maturation-associated protein	MAL	4118	ENSG00000172005			Mal (MGI:892970)			
chr2	95085390	95122026	2p11.2-q11.2	2q11.1		611972	MRPS5	Mitochondrial ribosomal protein S5	MRPS5	64969	ENSG00000144029			Mrps5 (MGI:1924971)			
chr2	95165416	95184316	2q11.2	2q11.1		194500	ZNF2	Zinc finger protein-2	ZNF2	7549	ENSG00000275111			Zfp661 (MGI:1919430)			
chr2	95274447	95291319	2q11.1	2q11.1		617160	"PROM2, PROML2"	Prominin 2	PROM2	150696	ENSG00000155066			Prom2 (MGI:2138997)			
chr2	95297323	95386076	2q11.1	2q11.1		604662	"KCNIP3, KCHIP3, CSEN, DREAM"	Potassium channel-interacting protein 3	KCNIP3	30818	ENSG00000115041			Kcnip3 (MGI:1929258)			
chr2	96021945	96035973	2q11.2	2q11.2		616431	GPAT2	"Glycerol-3-phosphate acyltransferase 2, mitochondrial"	GPAT2	150763	ENSG00000186281			Gpat2 (MGI:2684962)			
chr2	96112874	96116244	2q11.2	2q11.2		104260	"ADRA2B, ADRA2L1, FAME2"	"Adrenergic, alpha-2B-, receptor"	ADRA2B	151	ENSG00000274286		"Epilepsy, myoclonic, familial adult, 2, 607876 (3), Autosomal dominant"	Adra2b (MGI:87935)			
chr2	96143165	96145467	2q11	2q11.2		603068	"DUSP2, PAC1"	Dual-specificity phosphatase-2	DUSP2	1844	ENSG00000158050			Dusp2 (MGI:101911)			
chr2	96184858	96208845	2q11.2	2q11.2		616712	"STARD7, GTT1"	START domain-containing protein 4	STARD7	56910	ENSG00000084090			Stard7 (MGI:2139090)			
chr2	96248513	96266012	2q11	2q11.2		613403	TMEM127	Transmembrane protein 127	TMEM127	55654	ENSG00000135956		"{Pheochromocytoma, susceptibility to}, 171300 (3), Autosomal dominant"	Tmem127 (MGI:1916720)			
chr2	96266145	96274178	2q11.2	2q11.2		604333	"CIAO1, WDR39"	WD repeat-containing protein CIAO1	CIAO1	9391	ENSG00000144021			Ciao1 (MGI:1346998)			
chr2	96274335	96305568	2q11.2	2q11.2		601664	"SNRNP200, ASCC3L1, KIAA0788, RP33"	Small nuclear ribonucleoprotein 200kD (U5)	SNRNP200	23020	ENSG00000144028		"Retinitis pigmentosa 33, 610359 (3), Autosomal dominant"	Snrnp200 (MGI:2444401)			
chr2	96335740	96377094	2q11.2	2q11.2		602332	BRRN1	"Barren, Drosophila, homolog of, 1"	NCAPH	23397	ENSG00000121152			Ncaph (MGI:2444777)			
chr2	96497642	96508156	2p11	2q11.2		617206	"NEURL3, LINCR"	Neuralized E3 ubiquitin protein ligase 3	NEURL3	93082	ENSG00000163121			Neurl3 (MGI:2429944)			
chr2	96536718	96552637	2q11.2	2q11.2		611583	"ARID5A, MRF1"	AT-rich interactive domain-containing protein 5A	ARID5A	10865	ENSG00000196843			Arid5a (MGI:2443039)			
chr2	96593154	96638378	2q11.2	2q11.2		617742	"KANSL3, NSL3, KIAA1310"	"Kat8 regulatory NSL complex, subunit 3"	KANSL3	55683	ENSG00000114982			Kansl3 (MGI:1918055)			
chr2	96705928	96740091	2q11.2	2q11.2		609552	"LMAN2L, VIPL, MRT52"	LMAN2-like protein	LMAN2L	81562	ENSG00000114988	mutation identified in 1 MRT52 family	"?Mental retardation, autosomal recessive, 52, 616887 (3), Autosomal recessive"	Lman2l (MGI:2443010)			
chr2	96760901	96811890	2q11.2	2q11.2		607805	"CNNM4, ACDP4"	Cyclin M4	CNNM4	26504	ENSG00000158158		"Jalili syndrome, 217080 (3), Autosomal recessive"	Cnnm4 (MGI:2151060)			
chr2	96814945	96837108	2q11.2	2q11.2		607804	"CNNM3, ACDP3"	Cyclin M3	CNNM3	26505	ENSG00000168763	previously assigned to 2p12-p11.2		Cnnm3 (MGI:2151055)			
chr2	96837913	96844020	2p11.2-q11.1	2q11.2		610736	"ANKRD23, DARP"	Ankyrin repeat domain-containing protein 23	ANKRD23	200539	ENSG00000163126			Ankrd23 (MGI:1925571)			
chr2	96859735	96870942	5p15.3	2q11.2		604462	"SEMA4C, SEMAF, KIAA1739"	Semaphorin 4C	SEMA4C	54910	ENSG00000168758			Sema4c (MGI:109252)			
chr2	97646057	97648193	2cen-q13	2q11.2		123866	COX5B	"Cytochrome c oxidase, subunit Vb"	COX5B	1329	ENSG00000135940	"7 pseudogenes on 4, 6, 7, 11, 12, 13, and 22"					
chr2	97655938	97664097	2q11.1-q11.2	2q11.2		605144	"ACTR1B, ARP1B, CTRN2"	Actin-related protein 1B	ACTR1B	10120	ENSG00000115073			Actr1b (MGI:1917446)			
chr2	97712029	97744326	2q12	2q11.2		176947	"ZAP70, SRK, ADMIO2, IMD48"	"Zeta-chain associated protein kinase, 70kD (syk-related tyrosine kinase)"	ZAP70	7535	ENSG00000115085		"Autoimmune disease, multisystem, infantile-onset, 2, 617006 (3), Autosomal recessive; Immunodeficiency 48, 269840 (3), Autosomal recessive"	Zap70 (MGI:99613)			
chr2	97756335	97996181	2q11.2	2q11.2		615659	"TMEM131, KIAA0257, CC28"	Transmembrane protein 131	TMEM131	23505	ENSG00000075568			Tmem131 (MGI:1927110)			
chr2	98087131	98330681	2q11.2	2q11.2		614884	"VWA3B, SCAR22"	von Willebrand factor A domain-containing protein 3B	VWA3B	200403	ENSG00000168658	mutation identified in 1 SCAR22 family	"?Spinocerebellar ataxia, autosomal recessive 22, 616948 (3), Autosomal recessive"	Vwa3b (MGI:1918103)			
chr2	98346154	98399153	2q11	2q11.2		600053	"CNGA3, CNG3, ACHM2"	"Cyclic nucleotide-gated channel, alpha-3"	CNGA3	1261	ENSG00000144191		"Achromatopsia 2, 216900 (3), Autosomal recessive"	Cnga3 (MGI:1341818)			
chr2	98444537	98594067	2q11.2	2q11.2		600916	"INPP4A, INPP4"	"Inositol polyphosphate-4-phosphatase, type I, 107kD"	INPP4A	3631	ENSG00000040933			Inpp4a (MGI:1931123)			
chr2	98599322	98608517	2q11.2	2q11.2		613920	"COA5, C2orf64, PET191, CEMCOX3"	Cytochrome c oxidase assembly factor 5	COA5	493753	ENSG00000183513	mutation identified in 1 CEMCOX3 family	"?Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3, 616500 (3), Autosomal recessive"	Coa5 (MGI:1923428)			
chr2	98608547	98618514	2q11.2	2q11.2		617826	"UNC50, UNCL, GMH1"	"Unc50, inner nuclear membrane RNA-binding protein"	UNC50	25972	ENSG00000115446			Unc50 (MGI:1914637)			
chr2	98619105	98731125	2q12	2q11.2		604623	MGAT4A	"Alpha-1,3-mannosyl-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A"	MGAT4A	11320	ENSG00000071073			Mgat4a (MGI:2662992)			
chr2	98997260	99154965	2q11.2	2q11.2		607166	TSGA10	Testis-specific protein 10	TSGA10	80705	ENSG00000135951			Tsga10 (MGI:2685063)			
chr2	99154954	99163156	2q11.2	2q11.2		610284	"LIPT1, LIPT1D"	Lipoyltransferase 1	LIPT1	51601	ENSG00000144182		"Lipoyltransferase 1 deficiency, 616299 (3), Autosomal recessive"	Lipt1 (MGI:3645211)			
chr2	99181078	99199556	2q11.2	2q11.2		611838	"MRPL30, MRPL28"	Mitochondrial ribosomal protein L30	MRPL30	51263	ENSG00000185414			Mrpl30 (MGI:1333820)			
chr2	99242245	99260014	2q11.2	2q11.2		616547	"LYG2, LYSG2"	Lysozyme G-like 2	LYG2	254773	ENSG00000185674			Lyg2 (MGI:2685622)			
chr2	99306183	99336396	2q11.2	2q11.2		612564	"TXNDC9, PHLP3"	Thioredoxin domain-containing protein 9	TXNDC9	10190	ENSG00000115514			Txndc9 (MGI:2138153)			
chr2	99400474	99490122	2q11.2	2q11.2		606134	"REV1L, REV1"	"Rev1, S. cerevisiae, homolog of"	REV1	51455	ENSG00000135945			Rev1 (MGI:1929074)			
chr2	99545860	100142582	2q11.2-q12	2q11.2		601464	LAF4	Lymphoid nuclear protein related to AF4	AFF3	3899	ENSG00000144218			Aff3 (MGI:106927)			
chr2	100391859	100417667	2q11.2	2q11.2		606376	"CHST10, HNK1ST"	Carbohydrate sulfotransferase 10	CHST10	9486	ENSG00000115526			Chst10 (MGI:2138283)			
chr2	100562955	100577471	2q11.2	2q11.2		611678	"PDCL3, PHLP3, VIAF"	Phosducin-like 3	PDCL3	79031	ENSG00000115539			Pdcl3 (MGI:1916083)			
chr2	100820150	100996828	2q13	2q11.2		603347	"NPAS2, MOP4"	Neuronal PAS domain protein 2	NPAS2	4862	ENSG00000170485			Npas2 (MGI:109232)			
chr2	101002228	101019692	2q11.2	2q11.2		617415	RPL31	Ribosomal protein L31	RPL31	6160	ENSG00000071082			Rpl31 (MGI:2149632)			
chr2	101697702	101894689	2q11.2	2q11.2		604666	"MAP4K4, HGK, NIK, KIAA0687"	Mitogen-activated protein kinase kinase kinase kinase 4	MAP4K4	9448	ENSG00000071054			Map4k4 (MGI:1349394)			
chr2	101991804	102028543	2q12-q22	2q11.2		147811	"IL1R2, IL1RB"	"Interleukin-1 receptor, type II"	IL1R2	7850	ENSG00000115590			Il1r2 (MGI:96546)			
chr2	102069637	102179873	2q12	2q11.2-q12.1		147810	"IL1R1, IL1RA"	"Interleukin-1 receptor, type I"	IL1R1	3554	ENSG00000115594			Il1r1 (MGI:96545)			
chr2	102100000	129100000	2q12-q14			147185	"IGKV1OR2-108, IGO1"	Immunoglobulin orphon (transposed element) 1	IGKV1OR2-108	28862							
chr2	102100000	105300000	2q12.1			617071	LNC13	Long noncoding RNA 13									
chr2	102186972	102242909	2q12	2q12.1		604512	"IL1RL2, IL1RRP2"	Interleukin 1 receptor-like 2	IL1RL2	8808	ENSG00000115598			Il1rl2 (MGI:1913107)			
chr2	102311501	102352366	2q11.2	2q12.1		601203	IL1RL1	Interleukin 1 receptor-like 1	IL1RL1	9173	ENSG00000115602			Il1rl1 (MGI:98427)			
chr2	102355800	102398776	2q12	2q12.1		604494	"IL18R1, IL1RRP"	Interleukin 18 receptor 1	IL18R1	8809	ENSG00000115604			Il18r1 (MGI:105383)			
chr2	102418549	102452567	2q12	2q12.1		604509	"IL18RAP, ACPL"	Interleukin 18 receptor accessory protein	IL18RAP	8807	ENSG00000115607			Il18rap (MGI:1338888)			
chr2	102473281	102533973	2q12.1	2q12.1		600531	"SLC9A4, NHE4"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 4"	SLC9A4	389015	ENSG00000180251			Slc9a4 (MGI:105074)			
chr2	102619533	102711349	2q11.2	2q12.1		600530	SLC9A2	"Solute carrier family 9 (sodium/hydrogen exchanger), member 2"	SLC9A2	6549	ENSG00000115616			Slc9a2 (MGI:105075)			
chr2	104854067	104858573	2q12.1	2q12.1		602480	POU3F3	"POU domain, class 3, transcription factor-3"	POU3F3	5455	ENSG00000198914	previously mapped to 3p14.2		Pou3f3 (MGI:102564)			
chr2	105037468	105099959	2q12.1	2q12.1		611975	MRPS9	Mitochondrial ribosomal protein S9	MRPS9	64965	ENSG00000135972			Mrps9 (MGI:1916777)			
chr2	105241742	105243466	2q11.2-q12	2q12.1		604838	GPR45	G protein-coupled receptor 45	GPR45	11250	ENSG00000135973			Gpr45 (MGI:2135882)			
chr2	105249422	105329713	2q12.1	2q12.1-q12.2		606237	"TGFBRAP1, TRAP1"	Transforming growth factor-beta receptor-associated protein 1	TGFBRAP1	9392	ENSG00000135966			Tgfbrap1 (MGI:2447427)			
chr2	105360825	105438772	2q12-q14	2q12.2		602633	"FHL2, DRAL"	Four and a half LIM domains-2 (Down-regulated in rhabdomyosarcoma LIM protein)	FHL2	2274	ENSG00000115641			Fhl2 (MGI:1338762)			
chr2	105744648	105894273	2q12	2q12.2		604930	NCK2	NCK adaptor protein 2	NCK2	8440	ENSG00000071051			Nck2 (MGI:1306821)			
chr2	106063289	106078154	2q14.1-q14.3	2q12.2		611752	"C2orf40, ECRG4"	Esophageal cancer-related gene 4	C2orf40	84417	ENSG00000119147			1500015O10Rik (MGI:1926146)			
chr2	106093302	106194338	2q12	2q12.2		609749	"UXS1, UGD"	UDP-glucuronate decarboxylase 1	UXS1	80146	ENSG00000115652			Uxs1 (MGI:1915133)			
chr2	106382113	106391394	2q12.2	2q12.2		612212	"PLGLA, PRGA"	Plasminogen-like A	PLGLA	285189							
chr2	106404679	106470934	2q12.3-q13	2q12.2		612706	"RGPD3, RGP3"	RANBP2-like and GRIP domain-containing protein 3	RGPD3	653489	ENSG00000153165			Ranbp2 (MGI:894323)			
chr2	106700000	112200000	2q12.3-q13			612710	"RGPD7, RGP7"	RANBP2-like and GRIP domain-containing protein 7									
chr2	106801599	106887409	2q11.2-q12.1	2q12.3		608472	"ST6GALII, KIAA1877"	"Beta-galactoside alpha-2,6-sialyltransferase II"	ST6GAL2	84620	ENSG00000144057			St6gal2 (MGI:2445190)			
chr2	107826920	107892543	2q12.3-q13	2q12.3		612707	"RGPD4, RGP4"	RANBP2-like and GRIP domain-containing protein 4	RGPD4	285190	ENSG00000196862			Ranbp2 (MGI:894323)			
chr2	107986513	108014496	2q12.3	2q12.3		608761	"SLC5A7, CHT1, HMN7A, CMS20"	"Solute carrier family 5 (choline transporter), member 7"	SLC5A7	60482	ENSG00000115665		"Myasthenic syndrome, congenital, 20, presynaptic, 617143 (3), Autosomal recessive; Neuronopathy, distal hereditary motor, type VIIA, 158580 (3), Autosomal dominant"	Slc5a7 (MGI:1927126)			
chr2	108239991	108265607	2q12.2	2q12.3		617151	SULT1C3	"Sulfotransferase family 1C, member 3"	SULT1C3	442038	ENSG00000196228			Sult1c1 (MGI:102928)			
chr2	108288638	108309914	2q11.1-q11.2	2q12.3		602385	SULT1C1	Sulfotransferase 1C1	SULT1C2	6819	ENSG00000198203			Sult1c2 (MGI:1916333)			
chr2	108377910	108388988	2q11.2	2q12.3		608357	SULT1C2	"Sulfotransferase family 1C, member 2"	SULT1C4	27233	ENSG00000198075						
chr2	108448560	108509397	2q12.3	2q12.3		612711	"GCC2, GCC185, KIAA0336"	GRIP and coiled-coil domains-containing protein 2	GCC2	9648	ENSG00000135968			Gcc2 (MGI:1917547)			
chr2	108700000	112200000	2q13			257550	COMA	Cogan-type congenital oculomotor apraxia		266710		independent gene or feature of nephronophthisis	"Oculomotor apraxia, congenital, Cogan-type, 257550 (2), Autosomal recessive"				
chr2	108719445	109842300	2q11-q13	2q13		601181	"RANBP2, NUP358, ANE1, IIAE3"	RAN-binding protein 2	RANBP2	5903	ENSG00000153201		"{Encephalopathy, acute, infection-induced, 3, susceptibility to}, 608033 (3), Autosomal dominant"				
chr2	108894470	108989371	2q11-q13	2q13		604095	"EDAR, DL, ED3, EDA3, HRM1, ECTD10A, ECTD10B"	"Ectodysplasin 1, anhidrotic receptor (downless, mouse, homolog of)"	EDAR	10913	ENSG00000135960		"Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant, 129490 (3), Autosomal dominant; Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900 (3), Autosomal recessive; [Hair morphology 1, hair thickness], 612630 (3)"	Edar (MGI:1343498)			
chr2	109542796	109614205	2q13	2q13		611737	10-Sep	Septin 10	10-Sep	151011	ENSG00000186522	pseudogene on 8q22.1-q12		Sept10 (MGI:1918110)			
chr2	109760593	109857690	2q12.3-q13	2q13		612708	"RGPD5, RGP5, BS63"	RANBP2-like and GRIP domain-containing protein 5	RGPD5	84220	ENSG00000015568			Ranbp2 (MGI:894323)			
chr2	110083869	110118138	2q13	2q13		602022	"MALL, BENE"	"mal, T-cell differentiation protein-like"	MALL	7851	ENSG00000144063			Mall (MGI:2385152)			
chr2	110123335	110205061	2q13	2q13		607100	"NPHP1, NPH1, SLSN1, JBTS4"	Nephrocystin	NPHP1	4867	ENSG00000144061		"Joubert syndrome 4, 609583 (3), Autosomal recessive; Nephronophthisis 1, juvenile, 256100 (3), Autosomal recessive; Senior-Loken syndrome-1, 266900 (3), Autosomal recessive"	Nphp1 (MGI:1858233)			
chr2	110513801	110610902	2q12.3-q13	2q13		612709	"RGPD6, RGP6"	RANBP2-like and GRIP domain-containing protein 6	RGPD6	729540	ENSG00000183054			Ranbp2 (MGI:894323)			
chr2	110637697	110678106	2q14	2q13		602452	BUB1	"Budding uninhibited by benzimidazoles 1, S. cerevisiae, homolog of (mitotic checkpoint gene BUB1)"	BUB1	699	ENSG00000169679		"Colorectal cancer with chromosomal instability, somatic (3)"	Bub1 (MGI:1100510)			
chr2	111120913	111168444	2q13	2q13		603827	"BCL2L11, BIM"	BCL2-like 11	BCL2L11	10018	ENSG00000153094			Bcl2l11 (MGI:1197519)			
chr2	111195865	111495160	2q13	2q13		617144	"MIR4435-2HG, MORRBID"	MIR4435-2 host gene (long noncoding RNA MORRBID)	MIR4435-2HG	541471							
chr2	111766149	111884195	2q13	2q13		608473	"ANAP1, APC1"	"Anaphase-promoting complex, subunit 1"	ANAPC1	64682	ENSG00000153107			Anapc1 (MGI:103097)			
chr2	111898478	112039945	2q14.1	2q13		604705	"MERTK, RP38"	Mer tyrosine kinase protooncogene	MERTK	10461	ENSG00000153208		"Retinitis pigmentosa 38, 613862 (3), Autosomal recessive"	Mertk (MGI:96965)			
chr2	112055222	112119317	2q13	2q13		617203	TMEM87B	Transmembrane protein 87B	TMEM87B	84910	ENSG00000153214			Tmem87b (MGI:1919727)			
chr2	112138384	112254557	2q13	2q13-q14		611551	"FBLN7, TM14"	Fibulin 7	FBLN7	129804	ENSG00000144152			Fbln7 (MGI:1917620)			
chr2	112200000	118100000	2q14.1			612459	BMIQ13	Body mass index quantitative trait locus 13		100233157		associated with rs7566605	"[Body mass index QTL13], 612459 (2)"				
chr2	112200000	147900000	2q14-q22			604288	CMD1H	"Cardiomyopathy, dilated, 1H"	CMD1H	23459			"Cardiomyopathy, dilated, 1H, 604288 (2)"				
chr2	112200000	136100000	2q14-q21			165320	LCO	Liver cancer oncogene					?Hepatocellular carcinoma (1)				
chr2	112200000	136100000	2q14-q21			164755	"VIS1, HIS1"	Viral integration site 1	VIS1	7435							
chr2	112368368	112433644	2q12.3-q13	2q14.1		602752	"RGPD8, RGP8, RANBP2L1"	RANBP2-like and GRIP domain-containing protein 8	RGPD8	727851	ENSG00000169629			Ranbp2 (MGI:894323)			
chr2	112482126	112532645	2q13	2q14.1		608291	TTL	Tubulin-tyrosine ligase	TTL	150465	ENSG00000114999			Ttl (MGI:1916987)			
chr2	112541914	112577152	2q14.1	2q14.1		602000	POLR1B	"Polymerase I, RNA, subunit B"	POLR1B	84172	ENSG00000125630			Polr1b (MGI:108014)			
chr2	112584436	112589039	2q14.1	2q14.1		616978	"CHCHD5, MIC14"	Coiled coil-helix-coiled coil-helix domain-containing protein 5	CHCHD5	84269	ENSG00000125611			Chchd5 (MGI:1913420)			
chr2	112645856	112663824	2q11-q14	2q14.1		137570	"SLC20A1, GLVR1"	"Solute carrier family 20, phosphate transporter, member 1 (Gibbon ape leukemia virus receptor-1)"	SLC20A1	6574	ENSG00000144136			Slc20a1 (MGI:108392)			
chr2	112736348	112764676	2q13	2q14.1		616174	"CKAP2L, RADMIS"	Cytoskeleton-associated protein 2-like	CKAP2L	150468	ENSG00000169607		"Filippi syndrome, 272440 (3), Autosomal recessive"	Ckap2l (MGI:1917716)			
chr2	112773914	112785397	2q14	2q14.1		147760	IL1A	"Interleukin-1, alpha"	IL1A	3552	ENSG00000115008	"within 430kb of IL1B, IL1RN"		Il1a (MGI:96542)			
chr2	112829757	112836842	2q14	2q14.1		147720	IL1B	"Interleukin-1, beta"	IL1B	3553	ENSG00000125538	"within 430kb of IL1RN, IL1A"	"{Gastric cancer risk after H. pylori infection}, 137215 (3), Autosomal dominant"	Il1b (MGI:96543)			
chr2	112908884	112918881	2q12.1	2q14.1		605510	"IL37, IL1F7, FIL1Z, IL1H4, IL1RP1"	Interleukin 37	IL37	27178	ENSG00000125571						
chr2	112978018	112985671	2q13	2q14.1		605542	"IL36G, IL1F9, IL1H1, IL1RP2"	"Interleukin 36, gamma"	IL36G	56300	ENSG00000136688			Il1f9 (MGI:2449929)			
chr2	113005460	113011070	2q13	2q14.1		605509	"IL36A, IL1F6, FIL1E"	"Interleukin 36, alpha"	IL36A	27179	ENSG00000136694			Il1f6 (MGI:1859324)			
chr2	113022090	113052866	2q13	2q14.1		605508	"IL36B, IL1F8, IL1H2, FIL1H"	"Interleukin 36, beta"	IL36B	27177	ENSG00000136696			Il1f8 (MGI:1916927)			
chr2	113058637	113064743	2q13	2q14.1		605507	"IL36RN, IL1F5, FIL1D, IL1HY1, IL1RP3, PSORP, PSORS14"	Interleukin 36 receptor antagonist	IL36RN	26525	ENSG00000136695		"Psoriasis 14, pustular, 614204 (3), Autosomal recessive"	Il1f5 (MGI:1859325)			
chr2	113067969	113075849	2q14	2q14.1		615296	"IL1F10, IL1HY2"	"Interleukin 1 family, member 10"	IL1F10	84639	ENSG00000136697			Il1f10 (MGI:2652548)			
chr2	113099364	113134015	2q14.2	2q14.1		147679	"IL1RN, MVCD4, DIRA"	Interleukin-1 receptor antagonist	IL1RN	3557	ENSG00000136689		"{Gastric cancer risk after H. pylori infection}, 137215 (3), Autosomal dominant; Interleukin 1 receptor antagonist deficiency, 612852 (3), Autosomal recessive; {Microvascular complications of diabetes 4}, 612628 (3)"	Il1rn (MGI:96547)			
chr2	113157398	113203228	2q13	2q14.1		614442	"PSD4, EFA6B, TIC"	Pleckstrin and Sec7 domains-containing protein 4	PSD4	23550	ENSG00000125637			Psd4 (MGI:2674093)			
chr2	113215996	113278920	2q12-q14	2q14.1		167415	PAX8	Paired box homeotic gene-8	PAX8	7849	ENSG00000125618		"Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, 218700 (3), Autosomal dominant"	Pax8 (MGI:97492)			
chr2	113437690	113496203	2q13-q14.1	2q14.1		611079	CBWD2	Cobalamin synthetase W domain-containing protein 2	CBWD2	150472	ENSG00000215126						
chr2	113499083	113501149	2q13-q14.1	2q14.1		611084	FOXD4L1	Forkhead box D4-like 1	FOXD4L1	200350	ENSG00000184492						
chr2	113627217	113643397	2q13	2q14.1		605412	RABL2A	RAB-like 2A	RABL2A	11159	ENSG00000144134			Rabl2 (MGI:1915958)			
chr2	113889933	113961553	2q14.1	2q14.1		604222	"ACTR3, ARP3"	Actin-related protein 3	ACTR3	10096	ENSG00000115091			Actr3 (MGI:1921367)			
chr2	114442357	115845751	2q12.3-q14.2	2q14.1		608209	"DPP10, DPRP3, KIAA1492"	Dipeptidyl peptidase X	DPP10	57628	ENSG00000175497			Dpp10 (MGI:2442409)			
chr2	117814678	117832376	2q14.1	2q14.1		606355	DDX18	DEAD/H box 18	DDX18	8886	ENSG00000088205			Ddx18 (MGI:1914192)			
chr2	118088417	118110030	2q14.1	2q14.1-q14.2		608660	INSIG2	Insulin-induced gene 2	INSIG2	51141	ENSG00000125629			Insig2 (MGI:1920249)			
chr2	118842170	118848182	2q13-q21	2q14.2		131290	EN1	Engrailed-1	EN1	2019	ENSG00000163064			En1 (MGI:95389)			
chr2	118942168	118994663	2q12-q13	2q14.2		604870	MARCO	Macrophage receptor with collagenous structure	MARCO	8685	ENSG00000019169			Marco (MGI:1309998)			
chr2	119156242	119158894	2q14.2	2q14.2		614330	"C1QL2, CTRP10, C1QTNF10"	"Complement component 1, q subcomponent-like 2"	C1QL2	165257	ENSG00000144119			C1ql2 (MGI:3032521)			
chr2	119222475	119265651	2q14.2	2q14.2		609671	"STEAP3, TSAP6, AHMIO2"	Six-transmembrane epithelial antigen of prostate 3	STEAP3	55240	ENSG00000115107	mutation identified in 1 AHMIO2 family	"?Anemia, hypochromic microcytic, with iron overload 2, 615234 (3), Autosomal dominant"	Steap3 (MGI:1915678)			
chr2	119366923	119372550	2q12-q21	2q14.2		125950	DBI	Diazepam-binding inhibitor	DBI	1622	ENSG00000155368	?on 6q21-qter		Dbi (MGI:94865)			
chr2	119439842	119524451	2q14.1	2q14.2		182098	SCTR	Secretin receptor	SCTR	6344	ENSG00000080293			Sctr (MGI:2441720)			
chr2	119759630	119984898	2q14.2	2q14.2		176878	"PTPN4, PTPMEG1"	"Protein-tyrosine phosphatase, nonreceptor-type, 4"	PTPN4	5775	ENSG00000088179			Ptpn4 (MGI:1099792)			
chr2	120013027	120179120	2q14	2q14.2		611730	"EPB41L5, KIAA1548"	Erythrocyte membrane protein band 4.1-like 5	EPB41L5	57669	ENSG00000115109			Epb41l5 (MGI:103006)			
chr2	120252837	120294710	2cen-q13	2q14.2		179551	RALB	RAS-like protein B	RALB	5899	ENSG00000144118			Ralb (MGI:1927244)			
chr2	120346141	120351807	2cen-q13	2q14.2		147390	INHBB	"Inhibin, beta-2"	INHBB	3625	ENSG00000163083			Inhbb (MGI:96571)			
chr2	120735864	120992652	2q14	2q14.2		165230	"GLI2, HPE9, CJS"	GLI-Kruppel family member GLI2 (oncogene GLI2)	GLI2	2736	ENSG00000074047		"Culler-Jones syndrome, 615849 (3), Autosomal dominant; Holoprosencephaly 9, 610829 (3), Autosomal dominant"	Gli2 (MGI:95728)			
chr2	121216586	121285209	2q14	2q14.2		609785	"TFCP2L1, CRTR1, LBP9"	Transcription factor CP2-like 1	TFCP2L1	29842	ENSG00000115112			Tfcp2l1 (MGI:2444691)			
chr2	121337775	121649475	2q14	2q14.2-q14.3		605852	"CLASP1, KIAA0622"	CLIP-associated protein 1	CLASP1	23332	ENSG00000074054			Clasp1 (MGI:1923957)			
chr2	121530879	121531008	2q14.2	2q14.2		601428	"RNU4ATAC, U4ATAC, MOPD1, TALS, RFMN"	"RNA, U4, small nuclear, AT-AC form"	RNU4ATAC	100151683			"Microcephalic osteodysplastic primordial dwarfism, type I, 210710 (3), Autosomal recessive; Roifman syndrome, 616651 (3), Autosomal recessive"				
chr2	121600000	136100000	2q14.3-q21.3			614588	DYT21	Dystonia 21	DYT21	100885773			"Dystonia 21, 614588 (2), Autosomal dominant"				
chr2	121726944	121736926	2q14.3	2q14.3		611970	"NIFK, MKI67IP, NOPP34"	Nucleolar protein interacting with the FHA domain of MKI67	NIFK	84365	ENSG00000155438			Nifk (MGI:1915199)			
chr2	121755544	121767852	2q21.1	2q14.3		600575	TSN	Translin	TSN	7247	ENSG00000211460			Tsn (MGI:109263)			
chr2	124025286	124921200	2q14	2q14.3		610519	"CNTNAP5, CASPR5"	Contactin-associated protein-like 5	CNTNAP5	129684	ENSG00000155052			Cntnap5a (MGI:3643623)			
chr2	126655934	126696674	2q14-q21	2q14.3		110750	"GYPC, GE, GPC"	Glycophorin C	GYPC	2995	ENSG00000136732		"[Blood group, Gerbich], 616089 (3); {Malaria, resistance to}, 611162 (3)"	Gypc (MGI:1098566)			
chr2	127048022	127107326	2q14	2q14.3		601248	"BIN1, AMPHL, CNM2"	Box-dependent MYC-interacting protein-1 (amphiphysin-like)	BIN1	274	ENSG00000136717		"Centronuclear myopathy 2, 255200 (3), Autosomal recessive"	Bin1 (MGI:108092)			
chr2	127257289	127294175	2q21	2q14.3		133510	"ERCC3, XPB, TTD2"	"Excision-repair cross-complementing rodent repair deficiency, complementation group 3"	ERCC3	2071	ENSG00000163161		"Trichothiodystrophy 2, photosensitive, 616390 (3), Autosomal recessive; Xeroderma pigmentosum, group B, 610651 (3), Autosomal recessive"	Ercc3 (MGI:95414)			
chr2	127298668	127387532	2q14.3	2q14.3		609487	"MAP3K2, MEKK2"	Mitogen-activated protein kinase kinase kinase 2	MAP3K2	10746	ENSG00000169967			Map3k2 (MGI:1346873)			
chr2	127418142	127429245	2q13-q14	2q14.3		612283	"PROC, PC, THPH3, THPH4"	Protein C (inactivator of coagulation factors Va and VIIIa)	PROC	5624	ENSG00000115718		"Thrombophilia due to protein C deficiency, autosomal dominant, 176860 (3), Autosomal dominant; Thrombophilia due to protein C deficiency, autosomal recessive, 612304 (3), Autosomal recessive"	Proc (MGI:97771)			
chr2	127535688	127637727	2q21.1	2q14.3		606541	MYO7B	Myosin VIIb	MYO7B	4648	ENSG00000169994			Myo7b (MGI:107709)			
chr2	127638420	127681785	2q14.3	2q14.3		607908	"LIMS2, PINCH2, LGMD2W"	LIM and senescent cell antigen-like domains 2	LIMS2	55679	ENSG00000072163	mutation identified in 1 LGMD2W family	"Muscular dystrophy, limb-girdle, type 2W, 616827 (3), Autosomal recessive"	Lims2 (MGI:2385067)			
chr2	127645863	127652638	2q21	2q14.3		603071	GPR17	G protein-coupled receptor-17	GPR17	2840	ENSG00000144230			Gpr17 (MGI:3584514)			
chr2	127846265	127858154	2q14.3	2q14.3		606017	POLR2D	"Polymerase II, RNA, subunit D"	POLR2D	5433	ENSG00000144231			Polr2d (MGI:1916491)			
chr2	127941216	128028119	2q14.3	2q14.3		609697	SAP130	"Sin3A-associated protein, 130kD"	SAP130	79595	ENSG00000136715			Sap130 (MGI:1919782)			
chr2	128091179	128195676	2q14.3	2q14.3		605897	"UGGT1, HUGT1"	UDP-glucose glycoprotein glucosyltransferase 1	UGGT1	56886	ENSG00000136731			Uggt1 (MGI:2443162)			
chr2	128265479	128318596	2q21	2q14.3		604846	"HS6ST1, HS6ST, HH15"	Heparan sulfate 6-O-sulfotransferase 1	HS6ST1	9394	ENSG00000136720		"{Hypogonadotropic hypogonadism 15 with or without anosmia}, 614880 (3), Autosomal dominant"	Hs6st1 (MGI:1354958)			
chr2	129100000	131700000	2q21.1			612311	ADHD5	"Attention deficit-hyperactivity disorder, susceptibility to, 5"		100190790		max lod at rs985162	"{Attention deficit-hyperactivity disorder, susceptibility to, 5}, 612311 (2)"				
chr2	129100000	147900000	2q21.1-q22			608316	CHDS2	"Coronary heart disease, susceptibility to, 2"		387584			"{Coronary heart disease, susceptibility to, 2}, 608316 (2)"				
chr2	129100000	136100000	2q21			606240	NMTC3	Nonmedullary thyroid carcinoma 3		114568			"{Thyroid carcinoma, nonmedullary, 3}, 606240 (2), Autosomal dominant"				
chr2	129979661	129982737	2q21.1	2q21.1		612909	"RAB6C, WTH3"	Ras-associated protein RAB6C	RAB6C	84084	ENSG00000222014						
chr2	130151391	130182749	2q21.1	2q21.1		610457	"SMPD4, NSMASE3, KIAA1418"	"Sphingomyelin phosphodiesterase 4, neutral membrane"	SMPD4	55627	ENSG00000136699			Smpd4 (MGI:1924876)			
chr2	130181921	130190728	2q21.1	2q21.1		613450	"FAM128B, MOZART2B"	"Family with sequence similarity 128, member B"	MZT2B	80097	ENSG00000152082						
chr2	130337932	130342680	2q21.2	2q21.1		613734	"CCDC115, CCP1, CDG2O"	Coiled-coil domain-containing protein 115	CCDC115	84317	ENSG00000136710		"Congenital disorder of glycosylation, type IIo, 616828 (3), Autosomal recessive"	Ccdc115 (MGI:1916918)			
chr2	130342224	130347960	2q21.1	2q21.1		612981	"IMP4, BXDC4"	"Imp4, S. cerevisiae, homolog of"	IMP4	92856	ENSG00000136718			Imp4 (MGI:106572)			
chr2	130356006	130375408	2q21.1	2q21.1		606587	"PTPN18, BDP1"	"Protein-tyrosine phosphatase, nonreceptor-type, 18"	PTPN18	26469	ENSG00000072135			Ptpn18 (MGI:108410)			
chr2	130592164	130599574	2q21.1	2q21.1		605194	"CFC1, CRYPTIC, HTX2"	Cryptic protein	CFC1	55997	ENSG00000136698		"Heterotaxy, visceral, 2, autosomal, 605376 (3), Autosomal dominant"	Cfc1 (MGI:109448)			
chr2	130836915	131051513	2q22	2q21.1		605216	"ARHGEF4, ASEF"	RHO guanine nucleotide exchange factor 4	ARHGEF4	50649	ENSG00000136002			Arhgef4 (MGI:2442507)			
chr2	131209580	131265253	2q21.1	2q21.1		608914	"POTEE, POTE2"	"POTE ankyrin domain family, member E"	POTEE	445582	ENSG00000188219	5 POTE2 genes within 2Mb segment					
chr2	131469723	131493079	2q21.1	2q21.1		613449	"FAM128A, MOZART2A"	"Family with sequence similarity 128, member A"	MZT2A	653784	ENSG00000173272			Mzt2 (MGI:1922845)			
chr2	131476006	131482933	2q21.1	2q21.1		617878	"TUBA3D, KTCN9"	"Tubulin, alpha-3D"	TUBA3D	113457	ENSG00000075886		"Keratoconus 9, 617928 (3)"				
chr2	131592041	131626428	2q21.1	2q21.1		611266	"POTEKP, ACT, ACTBL3, POTEK, FKSG30"	"POTE ankyrin domain family, member K, pseudogene"	POTEKP	440915							
chr2	132415971	132646595	2q21-q22	2q21.2		602886	GPR39	G protein-coupled receptor-39	GPR39	2863	ENSG00000183840			Gpr39 (MGI:1918361)			
chr2	132643279	132671578	2q21.2	2q21.2		610450	"LYPD1, PHTS"	LY6/PLAUR domain-containing protein 1	LYPD1	116372	ENSG00000150551			Lypd1 (MGI:1919835)			
chr2	132671787	133675181	2q21.2	2q21.2		608789	"NCKAP5, NAP5"	NCK-associated protein 5	NCKAP5	344148	ENSG00000176771			Nckap5 (MGI:2686394)			
chr2	134119921	134454620	2q21	2q21.2-q21.3		601774	MGAT5	"Mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl- glucosaminyltransferase"	MGAT5	4249	ENSG00000152127			Mgat5 (MGI:894701)			
chr2	134918809	134959344	2p14-q21.3	2q21.3		603862	CCNT2	Cyclin T2	CCNT2	905	ENSG00000082258			Ccnt2 (MGI:1920199)			
chr2	135052264	135176666	2q21.3	2q21.3		602536	"RAB3GAP1, WARBM1, P130"	"RAB3 GTPase-activating protein, catalytic subunit"	RAB3GAP1	22930	ENSG00000115839		"Warburg micro syndrome 1, 600118 (3), Autosomal recessive"	Rab3gap1 (MGI:2445001)			
chr2	135164217	135531235	2q21.3	2q21.3		615655	ZRANB3	Zinc finger RANBP2-type domain-containing protein 3	ZRANB3	84083	ENSG00000121988			Zranb3 (MGI:1918362)			
chr2	135665396	135665477	2q21	2q21.3		611774	"MIR128-1, MIRN128-1, MIR128A"	Micro RNA 128-1	MIR128-1	406915							
chr2	135741618	135785062	2q21.3-q22.1	2q21.3		611216	"UBXN4, UBXD2, KIAA2042, ERASIN"	UBX domain protein 4	UBXN4	23190	ENSG00000144224			Ubxn4 (MGI:1915062)			
chr2	135787839	135837194	2q21	2q21.3		603202	"LCT, LAC, LPH"	Lactase (lactase-phlorizin hydrolase)	LCT	3938	ENSG00000115850		"Lactase deficiency, congenital, 223000 (3), Autosomal recessive"	Lct (MGI:104576)			
chr2	135839625	135876476	2q21	2q21.3		601806	MCM6	"Minichromosome maintenance deficient (mis5, S. pombe) 6"	MCM6	4175	ENSG00000076003	mutations in introns 9 and 13	"Lactase persistence/nonpersistence, 223100 (3), Autosomal dominant"	Mcm6 (MGI:1298227)			
chr2	135905880	135985683	2q21.3	2q21.3		603084	"DARS, HBSL, HBSL"	Aspartyl tRNA synthetase	DARS	1615	ENSG00000115866		"Hypomyelination with brainstem and spinal cord involvement and leg spasticity, 615281 (3), Autosomal recessive"	Dars (MGI:2442544)			
chr2	136100000	168900000	2q22-q24			611535	MAFD5	Major affective disorder 5		100188843			"{Major affective disorder 5}, 611535 (2)"				
chr2	136114348	136118154	2q21	2q22.1		162643	"CXCR4, D2S201E, NPY3R, WHIMS"	Chemokine (C-X-C motif) receptor 4 (neuropeptide Y receptor Y3)	CXCR4	7852	ENSG00000121966		"Myelokathexis, isolated (3); WHIM syndrome, 193670 (3), Autosomal dominant"	Cxcr4 (MGI:109563)			
chr2	137964067	138016363	2q22	2q22.1		605238	"HNMT, MRT51"	Histamine N-methyltransferase	HNMT	3176	ENSG00000150540		"{Asthma, susceptibility to}, 600807 (3), Autosomal dominant; Mental retardation, autosomal recessive 51, 616739 (3), Autosomal recessive"	Hnmt (MGI:2153181)			
chr2	138669156	138780240	2q22.1	2q22.1		604635	"NXPH2, NPH2"	Neuroxophilin 2	NXPH2	11249	ENSG00000144227			Nxph2 (MGI:107491)			
chr2	142877625	143042315	2q22.2	2q22.2		605197	"KYNU, KYNUU, VCRL2"	Kynureninase	KYNU	8942	ENSG00000115919	mutation identified in 1 KYNUU family	"?Hydroxykynureninuria, 236800 (3), Autosomal recessive; Vertebral, cardiac, renal, and limb defects syndrome 2, 617661 (3), Autosomal recessive"	Kynu (MGI:1918039)			
chr2	143070972	143768351	2q22.2-q22.3	2q22.2-q22.3		610578	"ARHGAP15, BM046"	Rho GTPase-activating protein 15	ARHGAP15	55843	ENSG00000075884			Arhgap15 (MGI:1923367)			
chr2	143945044	144333068	2q22	2q22.3		610165	GTDC1	Glycosyltransferase-like domain containing 1	GTDC1	79712	ENSG00000121964			Gtdc1 (MGI:2444269)			
chr2	144384374	144520390	2q22	2q22.3		605802	"ZEB2, ZFHX1B, SMADIP1, SIP1"	Zinc finger E box-binding homeobox 2	ZEB2	9839	ENSG00000169554		"Mowat-Wilson syndrome, 235730 (3), Autosomal dominant"	Zeb2 (MGI:1344407)			
chr2	147844516	147930826	2q22.2-q23.3	2q22.3-q23.1		102581	"ACVR2A, ACVR2"	"Activin A receptor, type IIA"	ACVR2A	92	ENSG00000121989			Acvr2a (MGI:102806)			
chr2	147900000	168900000	2q23-q24.3			603964	DFNA16	"Deafness, autosomal dominant 16"	DFNA16	1694			"Deafness, autosomal dominant 16, 603964 (2), Autosomal dominant"				
chr2	147900000	182100000	2q23-q31			605818	DFNB27	"Deafness, autosomal recessive 27"	DFNB27	23713			"Deafness, autosomal recessive 27, 605818 (2), Autosomal recessive"				
chr2	147930396	148021603	2q22-q23	2q23.1		603056	"ORC4, ORC4L"	"Origin recognition complex, subunit 4, S. cerevisiae, homolog of"	ORC4	5000	ENSG00000115947		"Meier-Gorlin syndrome 2, 613800 (3), Autosomal recessive"	Orc4 (MGI:1347043)			
chr2	148021010	148516922	2q23.1	2q23.1		611472	"MBD5, KIAA1461, MRD1"	Methyl-CpG-binding domain protein 5	MBD5	55777	ENSG00000204406		"Mental retardation, autosomal dominant 1, 156200 (3), Autosomal dominant"	Mbd5 (MGI:2138934)			
chr2	148644779	148788490	2q23.1	2q23.1		611000	EPC2	"Enhancer of polycomb, Drosophila, homolog of, 2"	EPC2	26122	ENSG00000135999			Epc2 (MGI:1278321)			
chr2	148875222	149026758	2q23.1	2q23.1-q23.2		604593	"KIF5C, NKHC2, CDCBM2"	Kinesin family member 5C	KIF5C	3800	ENSG00000168280		"Cortical dysplasia, complex, with other brain malformations 2, 615282 (3), Autosomal dominant"	Kif5c (MGI:1098269)			
chr2	149329984	149474147	2q23.1-q23.2	2q23.2		613359	LYPD6	LY6/PLAUR domain-containing protein 6	LYPD6	130574	ENSG00000187123			Lypd6 (MGI:2443848)			
chr2	149569632	149587815	2q23.2	2q23.2		611935	"C2orf25, MMADHC"	Chromosome 2 open reading frame 25	MMADHC	27249	ENSG00000168288		"Homocystinuria, cblD type, variant 1, 277410 (3), Autosomal recessive; Methylmalonic aciduria and homocystinuria, cblD type, 277410 (3), Autosomal recessive; Methylmalonic aciduria, cblD type, variant 2, 277410 (3), Autosomal recessive"	Mmadhc (MGI:1923786)			
chr2	150468192	150487694	2q23.3	2q23.3		602924	"RND3, RHOE, ARHE"	RHO family GTPase 3	RND3	390	ENSG00000115963			Rnd3 (MGI:1921444)			
chr2	151270464	151289915	2q23.3	2q23.3		603525	NMI	NMYC interactor	NMI	9111	ENSG00000123609	previously assigned to 22q13.3		Nmi (MGI:1928368)			
chr2	151357591	151380047	2q23.3	2q23.3		600410	TNFAIP6	"Tumor necrosis factor, alpha-induced protein-6"	TNFAIP6	7130	ENSG00000123610			Tnfaip6 (MGI:1195266)			
chr2	151485333	151734486	2q22	2q23.3		161650	"NEB, NEM2"	Nebulin	NEB	4703	ENSG00000183091		"Nemaline myopathy 2, autosomal recessive, 256030 (3), Autosomal recessive"	Neb (MGI:97292)			
chr2	151800965	151828494	2q23-q24.1	2q23.3		608960	ARL5	ADP-ribosylation factor-like 5	ARL5A	26225	ENSG00000162980			Arl5a (MGI:1922673)			
chr2	151832770	152099166	2q22-q23	2q23.3		601949	"CACNB4, EJM6, EA5, EIG9"	"Calcium channel, voltage-dependent, beta 4 subunit"	CACNB4	785	ENSG00000182389		"{Epilepsy, idiopathic generalized, susceptibility to, 9}, 607682 (3), Autosomal dominant; {Epilepsy, juvenile myoclonic, susceptibility to, 6}, 607682 (3), Autosomal dominant; Episodic ataxia, type 5, 613855 (3), Autosomal dominant"	Cacnb4 (MGI:103301)			
chr2	152116800	152175991	2q23.3	2q23.3		606244	STAM2	Signal-transducing adaptor molecule 2	STAM2	10254	ENSG00000115145			Stam2 (MGI:1929100)			
chr2	152335169	152649833	2q23.3	2q23.3		616285	"FMNL2, KIAA1902"	Formin-like 2	FMNL2	114793	ENSG00000157827			Fmnl2 (MGI:1918659)			
chr2	152651592	152718011	2q23.3	2q23.3		612941	"PRPF40A, HYPA, FNBP3, FBP11"	"Precursor mRNA-processing factor 40, S. cerevisiae, homolog of, A"	PRPF40A	55660	ENSG00000196504			Prpf40a (MGI:1860512)			
chr2	152717692	152761252	2q23.3	2q23.3		616495	"ARL6IP6, AIP6"	ADP-ribosylation factor-like 6-interacting protein 6	ARL6IP6	151188	ENSG00000177917			Arl6ip6 (MGI:1929507)			
chr2	153477337	153478807	2q23	2q23.3		612171	RPRM	Reprimo	RPRM	56475	ENSG00000177519			Rprm (MGI:1915124)			
chr2	153871897	154454176	2q24.1	2q23.3-q24.1		608369	"GALNT13, KIAA1918"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13	GALNT13	114805	ENSG00000144278			Galnt13 (MGI:2139447)			
chr2	154000000	196600000	2q24-q32			612108	FGQTL1	Fasting plasma glucose level QTL 1		100499165		associated with rs560887	"[Fasting plasma glucose level QTL 1], 612108 (2)"				
chr2	154000000	177100000	2q24.1-q31.1			610295	INTLQ2	Intelligence quantitative trait locus 3		100462723			"{Intelligence QTL3}, 610295 (2)"				
chr2	154000000	196600000	2q24-q32			156232	"MMDK, MDK"	"Mesomelic dysplasia, Kantaputra type"		10305			"Mesomelic dysplasia, Kantaputra type, 156232 (2), Autosomal dominant"				
chr2	154000000	158900000	2q24.1			612759	SYNSTH	Synesthesia		100301527		max lod at D2S142	"Synesthesia, 612759 (2)"				
chr2	154698580	154858351	2q24.1	2q24.1		601534	"KCNJ3, GIRK1"	"Potassium inwardly-rectifying channel, subfamily J, member 3"	KCNJ3	3760	ENSG00000162989			Kcnj3 (MGI:104742)			
chr2	156324431	156332774	2q22-q23	2q24.1		601828	"NR4A2, NURR1, NOT, TINUR"	"Nuclear receptor subfamily 4, group A, member 2"	NR4A2	4929	ENSG00000153234			Nr4a2 (MGI:1352456)			
chr2	156435289	156586402	2q24.1	2q24.1		138430	GPD2	Glycerol-3-phosphate dehydrogenase 2 (mitochondrial)	GPD2	2820	ENSG00000115159	pseudogene on 19	"{Diabetes, type 2, susceptibility to}, 125853 (3), Autosomal dominant"	Gpd2 (MGI:99778)			
chr2	157257597	157318490	2q24.2	2q24.1		615129	"GALNT5, GALNACT5"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 5	GALNT5	11227	ENSG00000136542			Galnt5 (MGI:2179403)			
chr2	157318612	157327712	2q24.1	2q24.1		610072	"ERMN, JN, KIAA1189"	Ermin	ERMN	57471	ENSG00000136541			Ermn (MGI:1925017)			
chr2	157412781	157444091	2q11.2	2q24.1		604448	"CYTIP, PSCDBP, HE"	Cytohesin 1 interacting protein	CYTIP	9595	ENSG00000115165			Cytip (MGI:2183535)			
chr2	157526766	157628886	2q24.1	2q24.1		608981	"ACVR1C, ALK7"	"Activin A receptor, type IC"	ACVR1C	130399	ENSG00000123612			Acvr1c (MGI:2661081)			
chr2	157736445	157875895	2q23-q24	2q24.1		102576	"ACVR1, ACVRLK2, ALK2, FOP"	"Activin A receptor, type I"	ACVR1	90	ENSG00000115170		"Fibrodysplasia ossificans progressiva, 135100 (3), Autosomal dominant"	Acvr1 (MGI:87911)			
chr2	157995178	158136153	2q24.1	2q24.1		617340	UPP2	Uridine phosphorylase 2	UPP2	151531	ENSG00000007001			Upp2 (MGI:1923904)			
chr2	158456879	158681428	2q23-q31	2q24.1		604276	PKP4	Plakophilin-4	PKP4	8502	ENSG00000144283			Pkp4 (MGI:109281)			
chr2	158968599	159232658	2q24.2	2q24.2		611397	"TANC1, KIAA1728"	"Tetratricopeptide repeat-, ankyrin repeat-, and coiled-coil-containing protein 1"	TANC1	85461	ENSG00000115183			Tanc1 (MGI:1914110)			
chr2	159315311	159712438	2q23-q24	2q24.2		605683	BAZ2B	"Bromodomain adjacent to zinc finger domain, 2B"	BAZ2B	29994	ENSG00000123636			Baz2b (MGI:2442782)			
chr2	159712456	159768582	2q24.2	2q24.2		613334	7-Mar	Membrane-associated RING-CH finger protein 7	7-Mar	64844	ENSG00000136536			March7 (MGI:1931053)			
chr2	159768627	159798254	2q24	2q24.2		612246	"CD302, DCL1, KIAA0022"	CD302 antigen	CD302	9936	ENSG00000241399			Cd302 (MGI:1913455)			
chr2	159932001	160062614	2q23-q24	2q24.2		604939	"PLA2R1, PLA2R"	Phospholipase A2 receptor 1	PLA2R1	22925	ENSG00000153246			Pla2r1 (MGI:102468)			
chr2	160099665	160200312	2q24.2	2q24.2		147558	"ITGB6, AI1H"	"Integrin, beta-6"	ITGB6	3694	ENSG00000115221		"Amelogenesis imperfecta, type IH, 616221 (3), Autosomal recessive"	Itgb6 (MGI:96615)			
chr2	160272150	160493982	2q24.2	2q24.2		602310	"RBMS1, MSSP, SCR2"	"RNA-binding motif protein, single strand-interacting, 1"	RBMS1	5937	ENSG00000153250			Rbms1 (MGI:1861774)			
chr2	161136954	161236175	2q24.2	2q24.2		603893	"TANK, ITRAF"	TRAF family member-associated NF-Kappa-B activator	TANK	10010	ENSG00000136560			Tank (MGI:107676)			
chr2	161308274	161411716	2q24.2	2q24.2		607173	"PSMD14, POH1, PAD1"	"Proteasome 26S subunit, non-ATPase, 14"	PSMD14	10213	ENSG00000115233			Psmd14 (MGI:1913284)			
chr2	161416093	161425866	2q23-q37	2q24.2		604616	TBR1	"T-box, brain, 1"	TBR1	10716	ENSG00000136535			Tbr1 (MGI:107404)			
chr2	161620962	161985275	2q23-q24	2q24.2		605556	SLC4A10	"Solute carrier family 4 (sodium bicarbonate cotransporter-like), member 10"	SLC4A10	57282	ENSG00000144290			Slc4a10 (MGI:2150150)			
chr2	161992240	162074541	2q23	2q24.2		102720	"DPP4, CD26, ADCP2"	Dipeptidylpeptidase IV (CD26; adenosine deaminase complexing protein-2)	DPP4	1803	ENSG00000197635			Dpp4 (MGI:94919)			
chr2	162142868	162152403	2q36-q37	2q24.2		138030	GCG	Glucagon	GCG	2641	ENSG00000115263		[?Hyperproglucagonemia] (1)				
chr2	162170683	162243556	2q23	2q24.2		600403	"FAP, FAPA"	"Fibroblast activation protein, alpha subunit"	FAP	2191	ENSG00000078098			Fap (MGI:109608)			
chr2	162267078	162318707	2q24	2q24.2		606951	"IFIH1, MDA5, AGS7, SGMRT1"	Interferon induced with helicase C domain 1	IFIH1	64135	ENSG00000115267		"Aicardi-Goutieres syndrome 7, 615846 (3), Autosomal dominant; Singleton-Merten syndrome 1, 182250 (3), Autosomal dominant"	Ifih1 (MGI:1918836)			
chr2	162318762	162377224	2q24.2	2q24.2		607030	GCA	Grancalcin	GCA	25801	ENSG00000115271			Gca (MGI:1918521)			
chr2	162371406	162838816	2q24.2	2q24.2		608169	"KCNH7, ERG3, HERG3, Kv11.3"	"Potassium channel, voltage-gated, subfamily H, member 7"	KCNH7	90134	ENSG00000184611			Kcnh7 (MGI:2159566)			
chr2	162900000	168900000	2q24.3			610155	IDDM19	"Diabetes mellitus, insulin-dependent, 19"				associated with rs1990760	"{Diabetes mellitus, insulin-dependent, 19}, 610155 (2)"				
chr2	163602610	163736154	4q22.1	2q24.3		605295	FIGN	Fidgetin	FIGN	55137	ENSG00000182263			Fign (MGI:1890647)			
chr2	164492405	164622958	2q22-q24	2q24.3		601524	GRB14	Growth factor receptor-bound protein 14	GRB14	2888	ENSG00000115290			Grb14 (MGI:1355324)			
chr2	164680184	164842167	2q24	2q24.3		610318	"COBLL1, COBLR1, KIAA0977"	COBL-like protein 1	COBLL1	22837	ENSG00000082438			Cobll1 (MGI:2442894)			
chr2	164898198	164955720	2q24.3	2q24.3		616526	SLC38A11	"Solute carrier family 38 (amino acid transporter), member 11"	SLC38A11	151258	ENSG00000169507			Slc38a11 (MGI:2443383)			
chr2	165087519	165204294	2q24	2q24.3		182391	SCN3A	"Sodium channel, voltage-gated, type III, alpha polypeptide"	SCN3A	6328	ENSG00000153253			Scn3a (MGI:98249)			
chr2	165208055	165392309	2q23-q24.3	2q24.3		182390	"SCN2A, SCN2A1, BFIC3, EIEE11, BFIS3, BFNIS"	"Sodium channel, voltage-gated, type II, alpha subunit"	SCN2A	6326	ENSG00000136531	4 related genes on chr.2	"Epileptic encephalopathy, early infantile, 11, 613721 (3), Autosomal dominant; Seizures, benign familial infantile, 3, 607745 (3), Autosomal dominant"	Scn2a (MGI:98248)			
chr2	165747802	165796351	2q24-q31	2q24.3		601756	"GALNT3, HHS, HFTC"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3	GALNT3	2591	ENSG00000115339		"Tumoral calcinosis, hyperphosphatemic, familial, 211900 (3), Autosomal recessive"	Galnt3 (MGI:894695)			
chr2	165873361	165953837	2q24.3	2q24.3		612014	"TTC21B, THM1, NPHP12, SRTD4, ATD4"	Tetratricopeptide repeat domain 21B	TTC21B	79809	ENSG00000123607		"Nephronophthisis 12, 613820 (3), Autosomal recessive, Autosomal dominant; Short-rib thoracic dysplasia 4 with or without polydactyly, 613819 (3), Autosomal recessive"	Ttc21b (MGI:1920918)			
chr2	165989159	166149215	2q24	2q24.3		182389	"SCN1A, GEFSP2, SMEI, FEB3A, EIEE6, FHM3"	"Sodium channel, voltage-gated, type I, alpha polypeptide"	SCN1A	6323	ENSG00000144285		"Epilepsy, generalized, with febrile seizures plus, type 2, 604403 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 6 (Dravet syndrome), 607208 (3), Autosomal dominant; Febrile seizures, familial, 3A, 604403 (3), Autosomal dominant; Migraine, familial hemiplegic, 3, 609634 (3), Autosomal dominant"	Scn1a (MGI:98246)			
chr2	166195184	166375986	2q24	2q24.3		603415	"SCN9A, NENA, PN1, FEB3B, GEFSP7, SFNP, HSAN2D"	"Sodium channel, voltage-gated, type IX, alpha subunit"	SCN9A	6335	ENSG00000169432		"{Dravet syndrome, modifier of}, 607208 (3), Autosomal dominant; Epilepsy, generalized, with febrile seizures plus, type 7, 613863 (3), Autosomal dominant; Erythermalgia, primary, 133020 (3), Autosomal dominant; Febrile seizures, familial, 3B, 613863 (3), Autosomal dominant; HSAN2D, autosomal recessive, 243000 (3), Autosomal recessive; Insensitivity to pain, congenital, 243000 (3), Autosomal recessive; Paroxysmal extreme pain disorder,, 167400 (3), Autosomal dominant; Small fiber neuropathy, 133020 (3), Autosomal dominant"	Scn9a (MGI:107636)			
chr2	166403572	166494263	2q21-q23	2q24.3		182392	"SCN7A, SCN6A"	"Sodium channel, voltage-gated, type VII, alpha polypeptide"	SCN7A	6332	ENSG00000136546			Scn7a (MGI:102965)			
chr2	166888486	167259752	2q24.3	2q24.3		609778	"CMYA3, XIRP2"	Cardiomyopathy-associated protein 3	XIRP2	129446	ENSG00000163092			Xirp2 (MGI:2685198)			
chr2	167293059	167870855	2q24.3	2q24.3		603093	B3GALT1	"UDP-GAL:beta-GlcNAc beta-1,3-galactosyltransferase, polypeptide 1"	B3GALT1	8708	ENSG00000172318			B3galt1 (MGI:1349403)			
chr2	167954019	168247594	2q24.3	2q24.3		607648	"STK39, SPAK"	Serine/threonine protein kinase 39	STK39	27347	ENSG00000198648			Stk39 (MGI:1858416)			
chr2	168455861	168775133	2q24.3	2q24.3		615336	"CERS6, LASS6"	Ceramide synthase 6	CERS6	253782	ENSG00000172292			Cers6 (MGI:2442564)			
chr2	168786538	168865338	2q31.1	2q24.3		607496	NOSTRIN	Nitric oxide synthase trafficker	NOSTRIN	115677	ENSG00000163072			Nostrin (MGI:3606242)			
chr2	168865044	168890442	2q31.1	2q24.3		609395	"SPC25, SPBC25"	"SPC25, NDC80 kinetochore complex component"	SPC25	57405	ENSG00000152253			Spc25 (MGI:1913692)			
chr2	168900000	177100000	2q31.1			613681	"DUP2q31.1, C2DUPq31.1"	Chromosome 2q31.1 duplication syndrome				duplication of 9 HOXD genes and MTX2	"Chromosome 2q31.1 duplication syndrome, 613681 (4), Autosomal dominant"				
chr2	168900000	182100000	2q31			600321	IDDM7	Insulin-dependent diabetes mellitus-7	IDDM7	3406			"{Diabetes mellitus, insulin-dependent, 7}, 600321 (2)"				
chr2	168900000	182100000	2q31			611147	PNKD2	Paroxysmal nonkinesigenic dyskinesia 2		100188328		between D2S2188 and D2S364	"Paroxysmal nonkinesigenic dyskinesia 2, 611147 (2), Autosomal dominant"				
chr2	168900000	182100000	2q31			606708	SHFM5	Split-hand/foot malformation 5	SHFM5	171157		between EVX2 and D2S294	"Split-hand/foot malformation 5, 606708 (2)"				
chr2	168901222	168909999	2q24-q32	2q31.1		608058	"G6PC2, IGRP"	"Glucose-6-phosphatase, catalytic, 2"	G6PC2	57818	ENSG00000152254			G6pc2 (MGI:1277193)			
chr2	168915467	169031395	2q24	2q31.1		603201	"ABCB11, BSEP, SPGP, PFIC2, BRIC2"	"ATP-binding cassette, subfamily B, member 11 (bile salt export pump)"	ABCB11	8647	ENSG00000073734		"Cholestasis, benign recurrent intrahepatic, 2, 605479 (3), Autosomal recessive; Cholestasis, progressive familial intrahepatic 2, 601847 (3), Autosomal recessive"	Abcb11 (MGI:1351619)			
chr2	169067034	169096166	2q31.1	2q31.1		612131	"DHRS9, RDHTBE"	"Short-chain dehydrogenase/reductase family, member 9"	DHRS9	10170	ENSG00000073737			Dhrs9 (MGI:2442798)			
chr2	169127108	169362611	2q24-q31	2q31.1		600073	"LRP2, DBS"	Low density lipoprotein-related protein 2	LRP2	4036	ENSG00000081479		"Donnai-Barrow syndrome, 222448 (3), Autosomal recessive"	Lrp2 (MGI:95794)			
chr2	169479495	169506654	2q31	2q31.1		603650	BBS5	BBS gene 5	BBS5	129880	ENSG00000163093		"Bardet-Biedl syndrome 5, 615983 (3), Autosomal recessive"	Bbs5 (MGI:1919819)			
chr2	169509701	169526261	2q31.1	2q31.1		607701	"KLHL41, KBTBD10, SARCOSIN, NEM9"	Kelch-like family member 41	KLHL41	10324	ENSG00000239474		"Nemaline myopathy 9, 615731 (3), Autosomal recessive"	Klhl41 (MGI:2683854)			
chr2	169527879	169573920	2q31.3	2q31.1		617529	"FASTKD1, KIAA1800"	Fast kinase domains 1	FASTKD1	79675	ENSG00000138399			Fastkd1 (MGI:2444596)			
chr2	169584339	169641405	2q31.1	2q31.1		606093	PPIG	Peptidyl-prolyl isomerase G (cyclophilin G)	PPIG	9360	ENSG00000138398			Ppig (MGI:2445173)			
chr2	169798811	169812063	2q31.1	2q31.1		109090	"SSB, LARP3"	Sjogren syndrome antigen B	SSB	6741	ENSG00000138385			Ssb (MGI:98423)			
chr2	169827461	170084130	2q31.1	2q31.1		613831	UBR3	Ubiquitin protein ligase E3 component N-recognin 3	UBR3	130507	ENSG00000144357			Ubr3 (MGI:1861100)			
chr2	170178144	170655163	2q31.1-q31.2	2q31.1		610040	MYO3B	Myosin IIIB	MYO3B	140469	ENSG00000071909			Myo3b (MGI:2448580)			
chr2	170714724	170717987	2q31.1	2q31.1		609391	SP5	Transcription factor Sp5	SP5	389058	ENSG00000204335			Sp5 (MGI:1927715)			
chr2	170813209	170861150	2q31	2q31.1		605363	"GAD1, SCP, CPSQ1"	"Glutamate decarboxylase-1, brain, 67kD"	GAD1	2571	ENSG00000128683	mutation identified in 1 CPSQ1 family	"?Cerebral palsy, spastic quadriplegic, 1, 603513 (3), Autosomal recessive"	Gad1 (MGI:95632)			
chr2	171434165	171491028	2q22.3-q35	2q31.1		612515	"DCAF17, C20orf37"	DDB1- and CUL4-associated factor 17	DCAF17	80067	ENSG00000115827		"Woodhouse-Sakati syndrome, 241080 (3), Autosomal recessive"	Dcaf17 (MGI:1923013)			
chr2	171687408	171750157	2q31.1	2q31.1		603331	"DYNC1I2, DNCI2, IC2"	"Dynein, cytoplasmic-1, intermediate chain-2"	DYNC1I2	1781	ENSG00000077380						
chr2	171783404	171894305	2q24	2q31.1		603667	"SLC25A12, ARALAR, EIEE39"	"Solute carrier family 25 (mitochondrial carrier, Aralar), member 12"	SLC25A12	8604	ENSG00000115840		"Epileptic encephalopathy, early infantile, 39, 612949 (3), Autosomal recessive"	Slc25a12 (MGI:1926080)			
chr2	171922424	171983685	2q31.2-q33.1	2q31.1		603053	HAT1	Histone acetyltransferase-1	HAT1	8520	ENSG00000128708			Hat1 (MGI:96013)			
chr2	171999896	172082429	2q31.1	2q31.1		610267	"METAP1D, MAP1D"	Methionyl aminopeptidase type 1D (mitochondrial)	METAP1D	254042	ENSG00000172878			Metap1d (MGI:1913809)			
chr2	172085479	172089673	2q32	2q31.1		600029	DLX1	Distal-less homeo box-1	DLX1	1745	ENSG00000144355			Dlx1 (MGI:94901)			
chr2	172099437	172102749	2q32	2q31.1		126255	"DLX2, TES1"	Distal-less homeo box-2	DLX2	1746	ENSG00000115844			Dlx2 (MGI:94902)			
chr2	172427353	172506454	2q31.1	2q31.1		147556	ITGA6	"Integrin, alpha-6"	ITGA6	3655	ENSG00000091409		"Epidermolysis bullosa, junctional, with pyloric stenosis, 226730 (3), Autosomal recessive"	Itga6 (MGI:96605)			
chr2	172555372	172672697	2q31.1	2q31.1		602524	PDK1	"Pyruvate dehydrogenase kinase, isoenzyme 1"	PDK1	5163	ENSG00000152256			Pdk1 (MGI:1926119)			
chr2	173075434	173268008	2q31.1	2q31.1		609479	"ZAK, MLTK, MRK, SFMMP, CNM6"	Leucine zipper- and sterile alpha motif-containing kinase	MAP3K20	51776	ENSG00000091436		"Centronuclear myopathy 6 with fiber-type disproportion, 617760 (3), Autosomal recessive; Split-foot malformation with mesoaxial polydactyly, 616890 (3), Autosomal recessive"	Map3k20 (MGI:2443258)			
chr2	173354832	173368989	2q31	2q31.1		609937	"CDCA7, JPO1, ICF3"	Cell division cycle-associated 7	CDCA7	83879	ENSG00000144354		"Immunodeficiency-centromeric instability-facial anomalies syndrome 3, 616910 (3)"	Cdca7 (MGI:1914203)			
chr2	173906458	173965701	2q31	2q31.1		601804	SP3	Sp3 transcription factor	SP3	6670	ENSG00000172845			Sp3 (MGI:1277166)			
chr2	174072446	174248669	2q31.1	2q31.1		611175	"OLA1, GTBP9"	OBG-like ATPase 1	OLA1	29789	ENSG00000138430			Ola1 (MGI:1914309)			
chr2	174348149	174395714	2q31.1	2q31.1		605228	CIR1	CBF1-interacting corepressor	CIR1	9541	ENSG00000138433			Cir1 (MGI:1914185)			
chr2	174395728	174430073	2q31.1	2q31.1		614967	"SCRN3, SES3"	Secernin 3	SCRN3	79634	ENSG00000144306			Scrn3 (MGI:1921866)			
chr2	174559573	174682898	2q31.1	2q31.1		602357	"WIPF1, WASPIP, WIP, WAS2"	"WAS/WASL-interacting protein family, member 1"	WIPF1	7456	ENSG00000115935	mutation identified in 1 WAS2 patient	"?Wiskott-Aldrich syndrome 2, 614493 (3)"	Wipf1 (MGI:2178801)			
chr2	174747591	174764471	2q24-q32	2q31.1		100690	"CHRNA1, ACHRD, CMS1B, CMS1A"	"Cholinergic receptor, nicotinic, alpha polypeptide-1, muscle"	CHRNA1	1134	ENSG00000138435		"Multiple pterygium syndrome, lethal type, 253290 (3), Autosomal recessive; Myasthenic syndrome, congenital, 1A, slow-channel, 601462 (3), Autosomal dominant; Myasthenic syndrome, congenital, 1B, fast-channel, 608930 (3), Autosomal recessive, Autosomal dominant"	Chrna1 (MGI:87885)			
chr2	174799313	175005378	2q31-q32.1	2q31.1		118423	"CHN1, CHN, ARHGAP2, RHOGAP2, DURS2"	"Chimerin 1 (GTPase-activating protein, rho, 2)"	CHN1	1123	ENSG00000128656		"Duane retraction syndrome 2, 604356 (3)"	Chn1 (MGI:1915674)			
chr2	175072249	175168205	2q32	2q31.1		123811	"ATF2, CREB2"	Activating transcription factor 2	ATF2	1386	ENSG00000115966			Atf2 (MGI:109349)			
chr2	175176257	175181761	2q31.1	2q31.1		602736	ATP5G3	"ATP synthase, mitochondrial, C subunit-3"	ATP5MC3	518	ENSG00000154518			Atp5g3 (MGI:2442035)			
chr2	175923861	176002900	2q31	2q31.1		610236	"LNP, KIAA1715"	Lunapark	LNPK	80856	ENSG00000144320			Lnpk (MGI:1918115)			
chr2	176080106	176083961	2q31-q32	2q31.1		142991	EVX2	Even-skipped homeo box-2	EVX2	344191	ENSG00000174279	13kb 5' to HOX4I		Evx2 (MGI:95462)			
chr2	176087486	176095937	2q31-q32	2q31.1		142989	"HOXD13, HOX4I, SPD1, BDSD"	Homeo box-D13	HOXD13	3239	ENSG00000128714	mutation identified in 1 BDSD family	"Brachydactyly, type D, 113200 (3), Autosomal dominant; Brachydactyly, type E, 113300 (3), Autosomal dominant; ?Brachydactyly-syndactyly syndrome, 610713 (3); Syndactyly, type V, 186300 (3), Autosomal dominant; Synpolydactyly 1, 186000 (3), Autosomal dominant"	Hoxd13 (MGI:96205)			
chr2	176099801	176100759	2q31-q32	2q31.1		142988	"HOXD12, HOX4H"	Homeo box-D12	HOXD12	3238	ENSG00000170178	upstream from HOX4A-G		Hoxd12 (MGI:96204)			
chr2	176107355	176109587	2q31-q32	2q31.1		142986	"HOXD11, HOX4F"	Homeo box-D11	HOXD11	3237	ENSG00000128713			Hoxd11 (MGI:96203)			
chr2	176116763	176119941	2q31-q32	2q31.1		142984	"HOXD10, HOX4D"	Homeo box-D10	HOXD10	3236	ENSG00000128710		"Charcot-Marie-Tooth disease, foot deformity of, 192950 (3), Autosomal dominant; Vertical talus, congenital, 192950 (3), Autosomal dominant"	Hoxd10 (MGI:96202)			
chr2	176122684	176124916	2q31-q32	2q31.1		142982	"HOXD9, HOX4C"	Homeo box-D9	HOXD9	3235	ENSG00000128709			Hoxd9 (MGI:96210)			
chr2	176129693	176132694	2q31-q32	2q31.1		142985	"HOXD8, HOX4E"	Homeo box-D8	HOXD8	3234	ENSG00000175879			Hoxd8 (MGI:96209)			
chr2	176150302	176150411	2q31	2q31.1		611576	"MIR10B, MIRN10B"	Micro RNA 10B	MIR10B	406903							
chr2	176150393	176156077	2q31-q32	2q31.1		142981	"HOXD4, HOX4B"	Homeo box-D4	HOXD4	3233	ENSG00000278500			Hoxd4 (MGI:96208)			
chr2	176157162	176173101	2q31-q32	2q31.1		142980	"HOXD3, HOX4A"	Homeo box-D3	HOXD3	3232	ENSG00000128652			Hoxd3 (MGI:96207)			
chr2	176188578	176190906	2q31-q32	2q31.1		142987	"HOXD1, HOX4G"	Homeo box-D1	HOXD1	3231	ENSG00000128645			Hoxd1 (MGI:96201)			
chr2	176269394	176338024	2q31.1	2q31.1		608555	MTX2	Metaxin 2	MTX2	10651	ENSG00000128654			Mtx2 (MGI:1859652)			
chr2	177100000	179700000	2q31.2			612345	DEL2q31	Chromosome 2q31.2 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 2q31.2 deletion syndrome, 612345 (4)"				
chr2	177212693	177223958	2q31.2	2q31.2		605372	"HNRPA3, D10S102, FBRNP"	Heterogeneous nuclear ribonucleoprotein A3	HNRNPA3	220988	ENSG00000170144						
chr2	177230302	177265130	2q31	2q31.2		600492	"NFE2L2, NRF2, IMDDHH"	"Nuclear factor, erythroid-derived 2-like 2"	NFE2L2	4780	ENSG00000116044		"Immunodeficiency, developmental delay, and hypohomocysteinemia, 617744 (3), Autosomal dominant"	Nfe2l2 (MGI:108420)			
chr2	177392742	177543835	2q31	2q31.2		603051	"AGPS, ADHAPS, RCDP3"	Alkylglycerone-phosphate synthase	AGPS	8540	ENSG00000018510		"Rhizomelic chondrodysplasia punctata, type 3, 600121 (3), Autosomal recessive"	Agps (MGI:2443065)			
chr2	177623248	178108338	2q31.2	2q31.2		604961	"PDE11A, PDE11A1, PDE11A2, PDE11A3, PPNAD2"	Phosphodiesterase 11A	PDE11A	50940	ENSG00000128655		"Pigmented nodular adrenocortical disease, primary, 2, 610475 (3), Autosomal dominant"	Pde11a (MGI:3036251)			
chr2	178112408	178129655	2q31.2	2q31.2		608888	RBM45	RNA binding motif protein 45	RBM45	129831	ENSG00000155636			Rbm45 (MGI:2387367)			
chr2	178194464	178399432	2q32.1	2q31.2		606734	"OSBPL6, ORP6"	Oxysterol-binding protein-like protein 6	OSBPL6	114880	ENSG00000079156			Osbpl6 (MGI:2139014)			
chr2	178431413	178451239	2q31.3	2q31.2		603424	"PRKRA, PACT, RAX, DYT16"	"Protein kinase, interferon-inducible double-stranded RNA-dependent activator"	PRKRA	8575	ENSG00000180228		"Dystonia 16, 612067 (3), Autosomal recessive"	Prkra (MGI:1344375)			
chr2	178450591	178467548	2q31.1-q31.3	2q31.2		610219	"PJVK, DFNB59"	Pejvakin	PJVK	494513	ENSG00000204311		"Deafness, autosomal recessive 59, 610220 (3), Autosomal recessive"	Pjvk (MGI:2685847)			
chr2	178463663	178480816	2q31.2	2q31.2		607062	"FKBP7, FKBP23"	FK506-binding protein 7	FKBP7	51661	ENSG00000079150			Fkbp7 (MGI:1336879)			
chr2	178480453	178516323	2q31.2	2q31.2		607774	"PLEKHA3, FAPP1"	"Pleckstrin homology domain-containing protein, family A, member 3"	PLEKHA3	65977	ENSG00000116095			Plekha3 (MGI:1932515)			
chr2	178525988	178807422	2q31	2q31.2		188840	"TTN, CMD1G, TMD, LGMD2J, MPRM, HMERF, SALMY"	Titin	TTN	7273	ENSG00000155657		"Cardiomyopathy, dilated, 1G, 604145 (3); Cardiomyopathy, familial hypertrophic, 9, 613765 (3), Autosomal dominant; Muscular dystrophy, limb-girdle, type 2J, 608807 (3), Autosomal recessive; Myopathy, proximal, with early respiratory muscle involvement, 603689 (3); Salih myopathy, 611705 (3), Autosomal recessive; Tibial muscular dystrophy, tardive, 600334 (3), Autosomal dominant"	Ttn (MGI:98864)			
chr2	178825307	179050130	2q31	2q31.2		616031	"CCDC141, CAMDI"	Coiled-coil domain-containing protein 141	CCDC141	285025	ENSG00000163492			Ccdc141 (MGI:1919735)			
chr2	179441981	179864549	2q31.2-q31.3	2q31.2-q31.3		612344	"ZNF385B, ZFN533"	Zinc finger protein 385B	ZNF385B	151126	ENSG00000144331			Zfp385b (MGI:2444734)			
chr2	179700000	188500000	2q31.3-q32.1			187370	DA10	"Arthrogryposis, distal, type 10"				max lod at D2S364	"Arthrogryposis, distal, type 10, 187370 (2), Autosomal dominant"				
chr2	179860835	179860907	2q31.3	2q31.3		614488	MIR1258	Micro RNA 1258	MIR1258	100302172		on opposite strand from ZNF385B					
chr2	179944875	180007295	2q31.3	2q31.3		615186	"CWC2, KIAA1604, NCM"	"CWC22 spliceosome-associated protein, X. cerevisiae, homolog of"	CWC22	57703	ENSG00000163510			Cwc22 (MGI:2136773)			
chr2	180692103	180916938	2q31.3	2q31.3		615568	"SCHLAP1, PCAT114, LINC00913"	"SWI/SNF complex antagonist associated with prostate cancer 1, noncoding"	SCHLAP1	101669767							
chr2	180980384	181063426	2q32.1	2q31.3		604151	"UBE2E3, UBCH9"	Ubiquitin-conjugating enzyme E2E 3	UBE2E3	10477	ENSG00000170035			Ube2e3 (MGI:107412)			
chr2	181456891	181538927	2q31-q32	2q31.3		192975	"ITGA4, CD49D"	"Integrin, alpha-4 (antigen CD49D, alpha-4 subunit of VLA-4 receptor)"	ITGA4	3676	ENSG00000115232			Itga4 (MGI:96603)			
chr2	181536671	181657106	2q31.3	2q31.3		608381	"CERKL, RP26"	Ceramide kinase-like	CERKL	375298	ENSG00000188452		"Retinitis pigmentosa 26, 608380 (3)"	Cerkl (MGI:3037816)			
chr2	181668294	181680664	2q32	2q31.3		601724	"NEUROD1, NIDDM"	Neurogenic differentiation 1	NEUROD1	4760			"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant; Maturity-onset diabetes of the young 6, 606394 (3)"	Neurod1 (MGI:1339708)			
chr2	181891715	181930737	2q31.3	2q31.3		118990	"SSFA2, CS1"	Sperm-specific antigen 2	SSFA2	6744	ENSG00000138434			Ssfa2 (MGI:1917849)			
chr2	181954240	182131381	2q32.1	2q31.3-q32.1		613240	"PPP1R1C, IPP5"	"Protein phosphatase 1, regulatory subunit 1C"	PPP1R1C	151242	ENSG00000150722			Ppp1r1c (MGI:1923185)			
chr2	182100000	196600000	2q32.1-q32.3			602087	ARVD4	Arrhythmogenic right ventricular dysplasia 4	ARVD4	425			"Arrhythmogenic right ventricular dysplasia 4, 602087 (2), Autosomal dominant"				
chr2	182100000	188500000	2q32.1			612361	SCZD14	Schizophrenia 14		100196913		associated with rs1344706	"{Schizophrenia, susceptibility to, 14}, 612361 (2)"				
chr2	182140034	182523374	2q32.1	2q32.1		171890	PDE1A	Phosphodiesterase-1A	PDE1A	5136	ENSG00000115252			Pde1a (MGI:1201792)			
chr2	182715978	182780024	2p23.1-p22.1	2q32.1		607987	"DNAJC10, ERDJ5, JPDI"	"DNAJ/HSP40 homolog, subfamily C, member 10"	DNAJC10	54431	ENSG00000077232			Dnajc10 (MGI:1914111)			
chr2	182833274	182866769	2q31-q33	2q32.1		605083	"FRZB, FRZB1, SRFP3, OS1"	Frizzled-related protein	FRZB	2487	ENSG00000162998		"{Osteoarthritis susceptibility 1}, 165720 (3), Multifactorial"	Frzb (MGI:892032)			
chr2	182924850	183038857	2q32.1-q32.2	2q32.1		604891	"NCKAP1, NAP1"	NCK-associated protein 1	NCKAP1	10787	ENSG00000061676			Nckap1 (MGI:1355333)			
chr2	183117479	183161683	2q32.1	2q32.1		608140	"NUP35, NP44"	"Nucleoporin, 35kD"	NUP35	129401	ENSG00000163002			Nup35 (MGI:1916732)			
chr2	184598365	184939486	2q32.1	2q32.1		612282	"ZNF804A, C2orf10"	Zinc finger protein 804A	ZNF804A	91752	ENSG00000170396			Zfp804a (MGI:2442949)			
chr2	185738835	185833288	2q32.1	2q32.1		615796	FSIP2	Fibrous sheath-interacting protein 2	FSIP2	401024	ENSG00000188738			Fsip2 (MGI:2664111)			
chr2	186590062	186680901	2q31	2q32.1		193210	"ITGAV, VNRA"	"Integrin, alpha-V (vitronectin receptor, alpha polypeptide)"	ITGAV	3685	ENSG00000138448			Itgav (MGI:96608)			
chr2	187341962	187448303	2q31-q32	2q32.1		114190	"CALCRL, CGRPR, CRLR"	Calcitonin receptor-like	CALCRL	10203	ENSG00000064989			Calcrl (MGI:1926944)			
chr2	187464229	187554504	2q31-q32.1	2q32.1		152310	"TFPI, LACI"	Tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)	TFPI	7035	ENSG00000003436			Tfpi (MGI:1095418)			
chr2	188291668	188595925	2q32.2-q33	2q32.1-q32.2		608165	"GULP1, CED6"	PTB domain-containing engulfment adaptor protein 1	GULP1	51454	ENSG00000144366			Gulp1 (MGI:1920407)			
chr2	188733737	188790103	2q33	2q32.2		606423	DIRC1	Disrupted in renal cancer 1	DIRC1	116093	ENSG00000174325						
chr2	188974372	189012745	2q32.2	2q32.2		120180	"COL3A1, EDSVASC"	"Collagen III, alpha-1 polypeptide"	COL3A1	1281	ENSG00000168542	in same 35kb segment as COL5A2	"Ehlers-Danlos syndrome, vascular type, 130050 (3), Autosomal dominant"	Col3a1 (MGI:88453)			
chr2	189031914	189225300	2q32.2	2q32.2		120190	"COL5A2, EDSCL2"	"Collagen V, alpha-2 polypeptide"	COL5A2	1290	ENSG00000204262	very close to COL3A1	"Ehlers-Danlos syndrome, classic type, 2, 130010 (3), Autosomal dominant"	Col5a2 (MGI:88458)			
chr2	189560589	189580810	2q32	2q32.2		604653	"SLC40A1, SLC11A3, FPN1, IREG1, HFE4"	"Solute carrier family 40 (iron-regulated transporter), member 1"	SLC40A1	30061	ENSG00000138449		"Hemochromatosis, type 4, 606069 (3), Autosomal dominant"	Slc40a1 (MGI:1315204)			
chr2	189674291	189763058	2q32.2	2q32.2		609803	FLJ25415	FLJ25415 gene	ANKAR	150709	ENSG00000151687			Ankar (MGI:2442559)			
chr2	189766266	189784370	2q32.2	2q32.2		610073	ORMDL1	ORM1-like protein 1	ORMDL1	94101	ENSG00000128699	pseudogene on 10p14		Ormdl1 (MGI:2181669)			
chr2	189784084	189877628	2q31-q33	2q32.2		600258	"PMS1, PMSL1, HNPCC3"	"Postmeiotic segregation increased, S. cerevisiae, like 1"	PMS1	5378	ENSG00000064933			Pms1 (MGI:1202302)			
chr2	189879478	190203483	2q32.2	2q32.2		615117	"C2orf88, SMAKAP"	Small membrane protein kinase A-anchoring protein	C2orf88	84281	ENSG00000187699			1700019D03Rik (MGI:1914330)			
chr2	190055699	190062728	2q32.2	2q32.2		601788	"GDF8, MSTN, MSLHP"	Growth differentiation factor-8 (myostatin)	MSTN	2660	ENSG00000138379		"Muscle hypertrophy, 614160 (3)"	Mstn (MGI:95691)			
chr2	190204633	190320044	2q32.2	2q32.2		610690	HIBCH	3-hydroxyisobutyryl-CoA hydrolase	HIBCH	26275	ENSG00000198130		"3-hydroxyisobutryl-CoA hydrolase deficiency, 250620 (3), Autosomal recessive"	Hibch (MGI:1923792)			
chr2	190343469	190371664	2q32	2q32.2		147263	INPP1	Inositol polyphosphate-1-phosphatase	INPP1	3628	ENSG00000151689			Inpp1 (MGI:104848)			
chr2	190408354	190502314	2q32.2	2q32.2		613476	"MFSD6, MMR2"	Major facilitator superfamily domain-containing protein 6	MFSD6	54842	ENSG00000151690			Mfsd6 (MGI:1922925)			
chr2	190454087	190607125	2q32.2	2q32.2		616497	"NEMP2, TMEM194B"	Nuclear envelope integral membrane protein 2	NEMP2	100131211	ENSG00000189362			Nemp2 (MGI:2444113)			
chr2	190648859	190692765	2q32.3-q33	2q32.2		600800	NAB1	"NGFI-A-binding protein, ERG1-binding protein"	NAB1	4664	ENSG00000138386			Nab1 (MGI:107564)			
chr2	190880820	190965551	2q32-q34	2q32.2		138280	"GLS, GLS1"	Glutaminase	GLS	2744	ENSG00000115419			Gls (MGI:95752)			
chr2	190968988	191014249	2q32.2-q32.3	2q32.2		600555	"STAT1, CANDF7, IMD31A, IMD31B, IMD31C"	Signal transducer and activator of transcription-1	STAT1	6772	ENSG00000115415		"Immunodeficiency 31A, mycobacteriosis, autosomal dominant, 614892 (3), Autosomal dominant; Immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive, 613796 (3), Autosomal recessive; Immunodeficiency 31C, autosomal dominant, 614162 (3), Autosomal dominant"	Stat1 (MGI:103063)			
chr2	191029575	191172683	2q32.2-q32.3	2q32.2-q32.3		600558	"STAT4, SLEB11"	Signal transducer and activator of transcription-4	STAT4	6775	ENSG00000138378		"{Systemic lupus erythematosus, susceptibility to, 11}, 612253 (3)"	Stat4 (MGI:103062)			
chr2	191245275	191425388	2q32	2q32.3		606537	MYO1B	Myosin IB	MYO1B	4430	ENSG00000128641			Myo1b (MGI:107752)			
chr2	191678071	191688521	2q32.3	2q32.3		612103	"OBFC2A, SSB2"	Oligonucleotide/oligosaccharide-binding fold-containing protein 2A	NABP1	64859	ENSG00000173559			Nabp1 (MGI:1923258)			
chr2	191834304	191847279	2q32-q33	2q32.3		606728	"CAVIN2, SDPR, SDR"	Caveolae-associated protein 2	CAVIN2	8436	ENSG00000168497			Cavin2 (MGI:99513)			
chr2	191948299	192194932	2q32-q33	2q32.3		605734	"TMEFF2, HPP1, TR"	Transmembrane protein with EGF-like and 2 follistatin-like domains 2	TMEFF2	23671	ENSG00000144339			Tmeff2 (MGI:1861735)			
chr2	192749844	192776898	2q32	2q32.3		605443	PCGEM1	Prostate-specific gene PCGEM1	PCGEM1	64002							
chr2	195737603	196068811	2q33.1	2q32.3		610061	"DNAH7, KIAA0944"	"Dynein, axonemal, heavy chain 7"	DNAH7	56171	ENSG00000118997			"Dnah7c,Dnah7b,Dnah7a (MGI:3639762,MGI:2684953,MGI:2685838)"			
chr2	196133582	196176502	2q32.3	2q32.3		604727	"STK17B, DRAK2"	Serine/threonine protein kinase 17b	STK17B	9262	ENSG00000081320			Stk17b (MGI:2138162)			
chr2	196194369	196593691	2q32.3	2q32.3		617245	"HECW2, NEDL2, KIAA1301, NDHSAL"	"HECT, C2, and WW domains-containing E3 ubiquitin-protein ligase 2"	HECW2	57520	ENSG00000138411		"Neurodevelopmental disorder with hypotonia, seizures, and absent language, 617268 (3), Autosomal dominant"	Hecw2 (MGI:2685817)			
chr2	196600000	202500000	2q33.1			612586	ANIB9	"Aneurysm, intracranial berry, 9"		100271688		associated with rs700651	"{Aneurysm, intracranial berry, 9}, 612586 (2)"				
chr2	196600000	220700000	2q33-q35			177500	CHE2	"Cholinesterase, serum, 2"				linkage to chr. 16 markers?					
chr2	196600000	230100000	2q33-q36			614280	EJM9	"Epilepsy, juvenile myoclonic, susceptibility to, 9"		100750238		max lod at D2S2248	"{Epilepsy, juvenile myoclonic, susceptibility to, 9}, 614280 (2), Autosomal dominant"				
chr2	196600000	208200000	2q33			610439	RLS4	"Restless legs syndrome, susceptibility to, 4"		100188813		between D2S311 and D2S317	"{Restless legs syndrome 4}, 610439 (2)"				
chr2	196763031	196799767	2q33.1	2q33.1		604888	"GTF3C3, TFIIIC102"	"General transcription factor 3C, polypeptide 3"	GTF3C3	9330	ENSG00000119041			Gtf3c3 (MGI:2138383)			
chr2	196833003	196926994	2q33.1	2q33.1		611655	"PGAP1, MRT42"	Post-GPI attachment to proteins 1	PGAP1	80055	ENSG00000197121		"Mental retardation, autosomal recessive 42, 615802 (3), Autosomal recessive"	Pgap1 (MGI:2443342)			
chr2	197391973	197435092	2q33.1	2q33.1		605590	"SF3B1, SF3B155, SAP155, MDS"	"Splicing factor 3B, subunit 1"	SF3B1	23451	ENSG00000115524		"Myelodysplastic syndrome, somatic, 614286 (3)"	Sf3b1 (MGI:1932339)			
chr2	197486583	197500273	2q33.1	2q33.1		118190	"HSPD1, SPG13, HSP60, HLD4"	Heat-shock 60kD protein 1	HSPD1	3329	ENSG00000144381		"Leukodystrophy, hypomyelinating, 4, 612233 (3), Autosomal recessive; Spastic paraplegia 13, autosomal dominant, 605280 (3), Autosomal dominant"	Hspd1 (MGI:96242)			
chr2	197499996	197503462	2q33.1	2q33.1		600141	"HSPE1, HSP10"	Heat-shock 10kD protein	HSPE1	3336	ENSG00000115541			Hspe1 (MGI:104680)			
chr2	197515570	197553698	2q33.1	2q33.1		609361	"MOB4, MOBKL3, PREI3, MOB1, MOB3"	"MOB family, member 4"	MOB4	25843	ENSG00000115540			Mob4 (MGI:104899)			
chr2	197705303	197708389	2q33.1	2q33.1		609728	"MARS2, SPAX3, COXPD25"	Methionyl-tRNA synthetase 2	MARS2	92935	ENSG00000247626	mutation identified in 1 COXPD25 family	"?Combined oxidative phosphorylation deficiency 25, 616430 (3), Autosomal recessive; Spastic ataxia 3, autosomal recessive, 611390 (3), Autosomal recessive"	Mars2 (MGI:2444136)			
chr2	197726878	197786311	2q33	2q33.1		606165	"BOLL, BOULE"	"BOL-like (Boule, Drosophila, homolog of)"	BOLL	66037	ENSG00000152430			Boll (MGI:1922638)			
chr2	197804701	198149883	2q33	2q33.1		600597	"PLDL1, PLCE, PLCL"	Phospholipase C-like 1	PLCL1	5334	ENSG00000115896			Plcl1 (MGI:3036262)			
chr2	199269499	199471265	2q33	2q33.1		608148	"SATB2, KIAA1034, GLSS"	Special AT-rich sequence-binding protein 2	SATB2	23314	ENSG00000119042		"Glass syndrome, 612313 (3), Autosomal dominant"	Satb2 (MGI:2679336)			
chr2	199663331	199851179	2q33.1	2q33.1		614308	"FTCDNL1, FONG"	Formiminotransferase cyclodeaminase N-terminal like	FTCDNL1	348751	ENSG00000226124						
chr2	199955316	199964124	2q33.1	2q33.1		617267	"MAIP1, C2orf47"	Matrix AAA peptidase-interacting protein 1	MAIP1	79568	ENSG00000162972			Maip1 (MGI:1915365)			
chr2	200305880	200482262	2q33.1	2q33.1		613817	"SPATS2L, SGNP"	Spermatogenesis-associated serine-rich protein 2-like	SPATS2L	26010	ENSG00000196141			Spats2l (MGI:1914448)			
chr2	200510197	200584094	2q33.1	2q33.1		612425	"SGOL2, SGO2, TRIPIN"	Shugoshin-like 2	SGO2	151246	ENSG00000163535			"Sgo2a,Sgo2b (MGI:1098767,MGI:3644562)"			
chr2	200585951	200677063	2q33	2q33.1		602841	AOX1	Aldehyde oxidase-1	AOX1	316	ENSG00000138356			Aox1 (MGI:88035)			
chr2	200853008	200864743	2q33	2q33.1		601951	"CLK1, CLK, STY"	CDC-like kinase 1	CLK1	1195	ENSG00000013441			Clk1 (MGI:107403)			
chr2	200870906	200889332	2q33	2q33.1		615811	PPIL3	Peptidyl-prolyl isomerase-like 3	PPIL3	53938	ENSG00000240344			Ppil3 (MGI:1917475)			
chr2	200889326	200903931	2q33	2q33.1		605778	NIF3L1	"Ngg1 interacting factor 3, S. pombe, homolog of, like 1"	NIF3L1	60491	ENSG00000196290			Nif3l1 (MGI:1929485)			
chr2	200910170	200963700	2q33	2q33.1		601182	"ORC2, ORC2L"	"Origin recognition complex, subunit 2, S. cerevisiae, homolog of"	ORC2	4999	ENSG00000115942			Orc2 (MGI:1328306)			
chr2	201071738	201085749	2q31.3	2q33.1		603839	NDUFB3	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 3"	NDUFB3	4709	ENSG00000119013	"pseudogenes on chr. 1, 9, and 14"	"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufb3 (MGI:1913745)			
chr2	201116103	201172687	2q33	2q33.1		603599	"CFLAR, FLIP, CASPER, FLAME1, CASH"	CASP8- and FADD-like apoptosis regulator	CFLAR	8837	ENSG00000003402			Cflar (MGI:1336166)			
chr2	201182880	201229405	2q33-q34	2q33.1		601762	"CASP10, MCH4, ALPS2"	"Caspase 10, apoptosis-related cysteine protease"	CASP10	843	ENSG00000003400		"Autoimmune lymphoproliferative syndrome, type II, 603909 (3), Autosomal dominant; Gastric cancer, somatic, 613659 (3); Lymphoma, non-Hodgkin, somatic, 605027 (3)"				
chr2	201233442	201287710	2q33	2q33.1		601763	"CASP8, MCH5, ALPS2B"	"Caspase 8, apoptosis-related cysteine protease"	CASP8	841	ENSG00000064012	mutation identified in 1 ALPS2B family	"?Autoimmune lymphoproliferative syndrome, type IIB, 607271 (3), Autosomal recessive; {Breast cancer, protection against}, 114480 (3), Autosomal dominant; Hepatocellular carcinoma, somatic, 114550 (3); {Lung cancer, protection against}, 211980 (3), Autosomal recessive"	Casp8 (MGI:1261423)			
chr2	201377206	201451595	2q33-q34	2q33.1		607334	"TRAK2, GRIF1, ALS2CR3, KIAA0549, OIP98"	Gamma-aminobutyric acid receptor-interacting factor 1	TRAK2	66008	ENSG00000115993			Trak2 (MGI:1918077)			
chr2	201451668	201480850	2q33-q34	2q33.1		607333	"STRADB, ILPIP, ALS2CR2"	STE20-related kinase adaptor beta	STRADB	55437	ENSG00000082146	pseudogenes on chromosomes 1 and 9		Stradb (MGI:2144047)			
chr2	201620183	201643528	2q33.2	2q33.1		614423	"TMEM237, ALS2CR4, JBTS14"	Transmembrane protein 237	TMEM237	65062	ENSG00000155755		"Joubert syndrome 14, 614424 (3), Autosomal recessive"	Tmem237 (MGI:2138365)			
chr2	201644873	201700262	2q31	2q33.1		606575	"MPP4, DLG6"	"Membrane protein, palmitoylated 4"	MPP4	58538	ENSG00000082126			Mpp4 (MGI:2386681)			
chr2	201700262	201781171	2q33	2q33.1		606352	"ALS2, ALSJ, PLSJ, IAHSP"	Alsin	ALS2	57679	ENSG00000003393		"Amyotrophic lateral sclerosis 2, juvenile, 205100 (3), Autosomal recessive; Primary lateral sclerosis, juvenile, 606353 (3), Autosomal recessive; Spastic paralysis, infantile onset ascending, 607225 (3), Autosomal recessive"	Als2 (MGI:1921268)			
chr2	201790323	201895549	2q33.1	2q33.1		616147	"CDK15, PFTAIRE2, ALS2CR7"	Cyclin-dependent kinase 15	CDK15	65061	ENSG00000138395			Cdk15 (MGI:3583944)			
chr2	202034586	202038436	2q33	2q33.1		603410	FZD7	"Frizzled, Drosophila, homolog of, 7"	FZD7	8324	ENSG00000155760			Fzd7 (MGI:108570)			
chr2	202206179	202238598	2q32.2-q33	2q33.1		601912	"SUMO1, UBL1, SMT3, OFC10"	Small ubiquitin-like modifier 1	SUMO1	7341	ENSG00000116030	mutation identified in 1 OFC10 patient	"?Orofacial cleft 10, 613705 (3), Isolated cases"	Sumo1 (MGI:1197010)			
chr2	202265715	202303660	2p33.1	2q33.1		616742	"NOP58, NOP5"	"Nop58, S. cerevisiae, homolog of"	NOP58	51602	ENSG00000055044			Nop58 (MGI:1933184)			
chr2	202376309	202567750	2q33	2q33.1-q33.2		600799	"BMPR2, PPH1, POVD1"	"Bone morphogenetic receptor, type II"	BMPR2	659	ENSG00000204217		"Pulmonary hypertension, familial primary, 1, with or without HHT, 178600 (3), Autosomal dominant; Pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated, 178600 (3), Autosomal dominant; Pulmonary venoocclusive disease 1, 265450 (3), Autosomal dominant"	Bmpr2 (MGI:1095407)			
chr2	202878918	202912225	2q33.2	2q33.2		616620	WDR12	WD repeat-containing protein 12	WDR12	55759	ENSG00000138442			Wdr12 (MGI:1927241)			
chr2	202912217	202988260	2q33	2q33.2		607586	"ALS2CR8, CARF"	"Amyotrophic lateral sclerosis 2 chromosome region, candidate 8 (calcium response factor)"	CARF	79800	ENSG00000138380			Carf (MGI:2182269)			
chr2	203013783	203225193	2q33-q34	2q33.2		609816	"NBEAL1, ALS2CR17"	Neurobeachin-like 1	NBEAL1	65065	ENSG00000144426			Nbeal1 (MGI:2444343)			
chr2	203706474	203739755	2q33-q34	2q33.2		186760	CD28	CD28 antigen (Tp44)	CD28	940	ENSG00000178562			Cd28 (MGI:88327)			
chr2	203867787	203873959	2q33	2q33.2		123890	"CTLA4, IDDM12, CELIAC3, ALPS5"	Cytotoxic T-lymphocyte-associated serine esterase-4	CTLA4	1493	ENSG00000163599		"Autoimmune lymphoproliferative syndrome, type V, 616100 (3), Autosomal dominant; {Celiac disease, susceptibility to, 3}, 609755 (3); {Diabetes mellitus, insulin-dependent, 12}, 601388 (3); {Hashimoto thyroiditis}, 140300 (3), Autosomal dominant; {Systemic lupus erythematosus, susceptibility to}, 152700 (3), Autosomal dominant"	Ctla4 (MGI:88556)			
chr2	203936747	203961576	2q33	2q33.2		604558	"ICOS, AILIM, CVID1"	Inducible costimulator	ICOS	29851	ENSG00000163600		"Immunodeficiency, common variable, 1, 607594 (3), Autosomal recessive"	Icos (MGI:1858745)			
chr2	204100000	208200000	2q33.3			610839	"OS4, GOA1"	Osteoarthritis susceptibility 4		100188821		max lod at D2S2358	"{Osteoarthritis susceptibility 4}, 610839 (2)"				
chr2	205682499	205798132	2q34	2q33.3		602070	"NRP2, VEGF1265R2, NPN2"	Neuropilin 2	NRP2	8828	ENSG00000118257			Nrp2 (MGI:1100492)			
chr2	206123078	206159518	2q33-q34	2q33.3		157655	NDUFS1	"NADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kD"	NDUFS1	4719	ENSG00000023228		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufs1 (MGI:2443241)			
chr2	206159593	206162928	2q33-q34	2q33.3		600655	"EEF1B2, EEF1B1"	"Eukaryotic translation elongation factor-1, beta-2"	EEF1B2	1933	ENSG00000114942	pseudogene on chr.15		Eef1b2 (MGI:1929520)			
chr2	206175315	206218046	2q33.3	2q33.3		600239	GPR1	G protein-coupled receptor-1	GPR1	2825	ENSG00000183671	conflicting assignment to 15q21.6		Gpr1 (MGI:2385324)			
chr2	206203375	206266242	2q33.3	2q33.3		617636	GPR1AS	GPR1 antisense RNA	GPR1-AS	101669764							
chr2	206273571	206314437	2q33.3	2q33.3		617059	"ZDBF2, KIAA1571"	Zinc finger DBF domain-containing protein 2	ZDBF2	57683	ENSG00000204186			Zdbf2 (MGI:1921134)			
chr2	206443543	206621129	2q33	2q33.3		603710	"ADAM23, MDC3"	A disintegrin and metalloproteinase domain 23	ADAM23	8745	ENSG00000114948			Adam23 (MGI:1345162)			
chr2	206765387	206796188	2q33.3	2q33.3		612322	"FASTKD2, KIAA0971"	FAST kinase domains 2	FASTKD2	22868	ENSG00000118246	mutation identified in 1 family	"?Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Fastkd2 (MGI:1922869)			
chr2	207074136	207173850	2q32	2q33.3		604865	"KLF7, UKLF"	Kruppel-like factor 7	KLF7	8609	ENSG00000118263			Klf7 (MGI:1935151)			
chr2	207529891	207605988	2q32.3-q34	2q33.3		123810	CREB1	cAMP-response element-binding protein-1	CREB1	1385	ENSG00000118260	fusion gene with EWSR1	"Histiocytoma, angiomatoid fibrous, somatic, 612160 (3)"	Creb1 (MGI:88494)			
chr2	207580630	207626052	2q33.3	2q33.3		615257	"METTL21A, FAM119A"	Methyltransferase-like 21A	METTL21A	151194	ENSG00000144401			Mettl21a (MGI:1914349)			
chr2	207753888	207769562	2q33-q34	2q33.3		601723	FZD5	"Polarity gene 'frizzled,' Drosophila, homolog of"	FZD5	7855	ENSG00000163251			Fzd5 (MGI:108571)			
chr2	208121606	208124588	2q33-q35	2q33.3		123690	"CRYGD, CRYG4, CTRCT4, CACA, CCA3, PCC"	"Crystallin, gamma D"	CRYGD	1421	ENSG00000118231		"Cataract 4, multiple types, 115700 (3), Autosomal dominant"	Crygd (MGI:88524)			
chr2	208128136	208139099	2q33-q35	2q33.3		123680	"CRYGC, CRYG3, CTRCT2, CCL"	"Crystallin, gamma C"	CRYGC	1420	ENSG00000163254		"Cataract 2, multiple types, 604307 (3), Autosomal dominant"	Crygc (MGI:88523)			
chr2	208142572	208146326	2q33-q35	2q33.3		123670	"CRYGB, CRYG2, CTRCT39"	"Crystallin, gamma B"	CRYGB	1419	ENSG00000182187		"Cataract 39, multiple types, autosomal dominant, 615188 (3), Autosomal dominant"	Crygb (MGI:88522)			
chr2	208160739	208163572	2q33-q35	2q33.3		123660	"CRYGA, CRYG1"	"Crystallin, gamma A"	CRYGA	1418	ENSG00000168582			Cryga (MGI:88521)			
chr2	208165346	208190257	2q34	2q33.3		615536	"C2orf80, GONDA1"	Chromosome 2 open reading frame 80	C2orf80	389073	ENSG00000188674			D630023F18Rik (MGI:2138198)			
chr2	208200000	230100000	2q34-q36			185900	"DUP2q35, C2DUPq35, SDTY1, SD1"	"Chromosome 2q35 duplication syndrome (syndactyly, type I)"					"Syndactyly, type 1, with or without craniosynostosis, 185900 (4), Autosomal dominant"				
chr2	208200000	214500000	2q34			601318	IDDM13	Insulin-dependent diabetes mellitus-13	IDDM13	3412			"{Diabetes mellitus, insulin-dependent, 13}, 601318 (2)"				
chr2	208200000	220700000	2q34-q35			607966	SLEN2	"Systemic lupus erythematosus with nephritis, susceptibility to, 2"	SLEN2	192679			"{Systemic lupus erythematosus with nephritis, susceptibility to, 2}, 607966 (2)"				
chr2	208200000	214500000	2q34			186860	TCL4	T-cell leukemia/lymphoma-4	TCL4	6946			"Leukemia/lymphoma, T-cell, 186860 (2)"				
chr2	208236226	208255142	2q33.3	2q34		147700	IDH1	"Isocitrate dehydrogenase, soluble"	IDH1	3417	ENSG00000138413		"{Glioma, susceptibility to, somatic}, 137800 (3)"	Idh1 (MGI:96413)			
chr2	208266177	208358750	2q35	2q34		609414	"PIKFYVE, PIP5K3"	"Phosphatidylinositol kinase, FYVE-finger containing"	PIKFYVE	200576	ENSG00000115020		"Corneal fleck dystrophy, 121850 (3), Autosomal dominant"	Pikfyve (MGI:1335106)			
chr2	208359844	208494505	2q33	2q34		601469	PTHR2	Parathyroid hormone receptor 2	PTH2R	5746	ENSG00000144407			Pth2r (MGI:2180917)			
chr2	209424046	209734117	2q34-q35	2q34		157130	MAP2	Microtubule-associated protein-2	MAP2	4133	ENSG00000078018			Map2 (MGI:97175)			
chr2	209771924	209999299	2q35	2q34		612636	"UNC80, C2orf21, KIAA1843"	"Unc-80 homolog, NALCN activator"	UNC80	285175	ENSG00000144406		"Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, 616801 (3), Autosomal recessive"	Unc80 (MGI:2652882)			
chr2	210002564	210023362	2q32-q33.3	2q34		180480	RPE	Ribulose 5-phosphate 3-epimerase	RPE	6120	ENSG00000197713			Rpe (MGI:1913896)			
chr2	210021420	210171369	2q34	2q34		613833	"KANSL1L, C2orf67, MSL1V2"	KAT8 regulatory NSL complex subunit 1-like	KANSL1L	151050	ENSG00000144445			Kansl1l (MGI:1915941)			
chr2	210187989	210225490	2q34-q35	2q34		609576	"ACADL, LCAD"	"Acyl-Coenzyme A dehydrogenase, long chain"	ACADL	33	ENSG00000115361			Acadl (MGI:87866)			
chr2	210290143	210315170	2q32.1-qter	2q34		160780	MYL1	"Myosin, light polypeptide-1, alkali; skeletal, fast"	MYL1	4632	ENSG00000168530			Myl1 (MGI:97269)			
chr2	210431248	210477617	2q34	2q34		604155	"LANCL1, GPR69A"	LanC-like 1 (G protein-coupled receptor 69A)	LANCL1	10314	ENSG00000115365			Lancl1 (MGI:1336997)			
chr2	210477681	210679106	2q35	2q34		608307	"CPS1, PHN"	"Carbamoyl-phosphate synthetase 1, mitochondrial"	CPS1	1373	ENSG00000021826	urea cycle enzyme	"Carbamoylphosphate synthetase I deficiency, 237300 (3), Autosomal recessive; {Pulmonary hypertension, neonatal, susceptibility to}, 615371 (3); {Venoocclusive disease after bone marrow transplantation} (3)"	Cps1 (MGI:891996)			
chr2	211375716	212538627	2q34	2q34		600543	"ERBB4, HER4, ALS19"	Avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4	ERBB4	2066	ENSG00000178568		"Amyotrophic lateral sclerosis 19, 615515 (3), Autosomal dominant"	Erbb4 (MGI:104771)			
chr2	212999683	213155296	2q34	2q34		606234	"IKZF2, ANF1A2, HELIOS"	Ikaros family zinc finger 2	IKZF2	22807	ENSG00000030419			Ikzf2 (MGI:1342541)			
chr2	213284368	214410500	2q34	2q34		612173	"SPAG16, PF20"	Sperm-associated antigen 16	SPAG16	79582	ENSG00000144451			Spag16 (MGI:1913972)			
chr2	214500000	220700000	2q35			607949	MTBS1	"Mycobacterium tuberculosis, susceptibility to infection by"		404716			"{Tuberculosis, susceptibility to}, 607949 (2)"				
chr2	214500000	220700000	2q35			613016	NBLST5	"Neuroblastoma, susceptibility to, 5"		100306938		"associated with rs6435862, rs3768716"	"{Neuroblastoma, susceptibility to, 5}, 613016 (2)"				
chr2	214500000	230100000	2q35-q36			609153	PSHK2	"Pseudohyperkalemia, familial, 2, due to red cell leak"				max lod at D2S1338	"Pseudohyperkalemia, familial, 2, due to red cell leak, 609153 (2), Autosomal dominant"				
chr2	214725644	214809710	2q34-q35	2q35		601593	BARD1	BRCA1-associated RING domain 1	BARD1	580	ENSG00000138376		"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant"	Bard1 (MGI:1328361)			
chr2	214931541	215138590	2q34	2q35		607800	"ABCA12, ARCI4A, ARCI4B, ICR2B, LI2"	"ATP-binding cassette, subfamily A, member 12"	ABCA12	26154	ENSG00000144452		"Ichthyosis, congenital, autosomal recessive 4A, 601277 (3), Autosomal recessive; Ichthyosis, congenital, autosomal recessive 4B (harlequin), 242500 (3), Autosomal recessive"	Abca12 (MGI:2676312)			
chr2	215311955	215359744	2q35	2q35		601731	"ATIC, PURH, AICAR"	5-aminoimidazole-4-carboxyamide ribonucleotide formyltransferase/IMP cyclohydrolase	ATIC	471	ENSG00000138363		"AICA-ribosiduria due to ATIC deficiency, 608688 (3), Autosomal recessive"	Atic (MGI:1351352)			
chr2	215360439	215436166	2q34	2q35		135600	"FN1, FN, LETS, FNZ, GFND2, SMDCF"	Fibronectin-1	FN1	2335	ENSG00000115414		"Glomerulopathy with fibronectin deposits 2, 601894 (3), Autosomal dominant; Plasma fibronectin deficiency, 614101 (1), Autosomal dominant; Spondylometaphyseal dysplasia, corner fracture type, 184255 (3), Autosomal dominant"	Fn1 (MGI:95566)			
chr2	215939096	216013622	2q35	2q35		609207	"MREG, DSU"	Melanoregulin	MREG	55686	ENSG00000118242			Mreg (MGI:2151839)			
chr2	216031655	216081842	2q35	2q35		605843	"PECR, TERP"	Peroxisomal trans-2-enoyl-CoA reductase	PECR	55825	ENSG00000115425			Pecr (MGI:2148199)			
chr2	216109296	216206292	2q35	2q35		194364	XRCC5	"X-ray repair, complementing defective, repair in Chinese hamster cells-5"	XRCC5	7520	ENSG00000079246	included in YAC contig spanning 2q33-q34		Xrcc5 (MGI:104517)			
chr2	216257861	216372026	2q35	2q35		608208	"MARCH4, RNF174, KIAA1399"	Membrane-associated RING-CH finger protein 4	4-Mar	57574	ENSG00000144583			March4 (MGI:2683550)			
chr2	216412413	216483052	2q34-q36	2q35		606622	"SMARCAL1, HARP, SIOD"	"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A-like"	SMARCAL1	50485	ENSG00000138375		"Schimke immunoosseous dysplasia, 242900 (3), Autosomal recessive"	Smarcal1 (MGI:1859183)			
chr2	216498796	216501466	2q35	2q35		613314	RPL37A	Ribosomal protein L37A	RPL37A	6168	ENSG00000197756			Rpl37a (MGI:98068)			
chr2	216632827	216664435	2q33-q34	2q35		146731	IGFBP2	"Insulin-like growth factor-binding protein-2, 36kD"	IGFBP2	3485	ENSG00000115457			Igfbp2 (MGI:96437)			
chr2	216672104	216695548	2q33-q36	2q35		146734	"IGFBP5, IBP5"	Insulin-like growth factor-binding protein 5	IGFBP5	3488	ENSG00000115461			Igfbp5 (MGI:96440)			
chr2	216859457	216860058	2q35-q36	2q35		190231	TNP1	Transition protein-1	TNP1	7141	ENSG00000118245						
chr2	217799788	218002994	2q35-q36	2q35		600076	"TNS1, TNS"	Tensin 1	TNS1	7145	ENSG00000079308			Tns1 (MGI:104552)			
chr2	218125289	218137252	2q35	2q35		146928	"CXCR2, IL8RB, IL8R2"	"Chemokine, CXC motif, receptor 2"	CXCR2	3579	ENSG00000180871			Cxcr2 (MGI:105303)			
chr2	218162844	218166992	2q35	2q35		146929	"CXCR1, IL8RA"	"Chemokine, CXC motif, receptor 1"	CXCR1	3577	ENSG00000163464		"{AIDS, slow progression to}, 609423 (3)"	Cxcr1 (MGI:2448715)			
chr2	218217093	218254347	2q35	2q35		604224	"ARPC2, ARC34"	"Actin-related protein 2/3 complex, subunit 2"	ARPC2	10109	ENSG00000163466			Arpc2 (MGI:1923959)			
chr2	218259495	218263860	2q35	2q35		610147	"GPBAR1, BG37"	G protein-coupled bile acid receptor 1	GPBAR1	151306	ENSG00000179921			Gpbar1 (MGI:2653863)			
chr2	218264126	218270208	2q35	2q35		603488	AAMP	Angio-associated migratory cell protein	AAMP	14	ENSG00000127837			Aamp (MGI:107809)			
chr2	218270391	218346792	2q35	2q35		609023	"MR1, TAHCCP2, KIPP1184, BRP17, PNKD1, FPD1, PDC, DYT8"	Myofibrillogenesis regulator 1	PNKD	25953	ENSG00000127838		"Paroxysmal nonkinesigenic dyskinesia 1, 118800 (3), Autosomal dominant"	Pnkd (MGI:1930773)			
chr2	218274191	218292576	2q35	2q35		610364	"TMBIM1, RECS1"	Transmembrane BAX inhibitor motif-containing protein 1	TMBIM1	64114	ENSG00000135926			Tmbim1 (MGI:1916910)			
chr2	218381765	218396893	2q35	2q35		600266	"NRAMP1, NRAMP, SLC11A1"	"Solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1"	SLC11A1	6556	ENSG00000018280	within 220 kb of VIL1	"{Buruli ulcer, susceptibility to}, 610446 (3); {Mycobacterium tuberculosis, susceptibility to infection by}, 607948 (3)"	Slc11a1 (MGI:1345275)			
chr2	218398337	218405940	2q34	2q35		605323	"CTDSP1, NLIIF, SCP1"	"C-terminal domain of RNA polymerase II polypeptide A, small phosphatase of, 1"	CTDSP1	58190	ENSG00000144579			Ctdsp1 (MGI:2654470)			
chr2	218402645	218402721	2q35	2q35		612152	"MIR26B, MIRN26B"	Micro RNA 26B	MIR26B	407017							
chr2	218419114	218449524	2q35-q36	2q35		193040	VIL1	Villin-1	VIL1	7429	ENSG00000127831		"Cholestasis, progressive canalicular (1)"	Vil1 (MGI:98930)			
chr2	218568577	218596434	2q35	2q35		612054	"RQCD1, RCD1, CNOT9"	"Required for cell differentiation 1, S. pombe, homolog of"	CNOT9	9125	ENSG00000144580			Cnot9 (MGI:1928902)			
chr2	218637915	218659631	2q34-q35	2q35		604083	ZNF142	Zinc finger protein-142	ZNF142	7701	ENSG00000115568			Zfp142 (MGI:1924514)			
chr2	218659655	218663442	2q33	2q35		603647	"BCS1L, FLNMS, GRACILE, BJS, PTD, MC3DN1"	"bcs1, S. cerevisiae, homolog-like"	BCS1L	617	ENSG00000074582		"Bjornstad syndrome, 262000 (3), Autosomal recessive; GRACILE syndrome, 603358 (3); Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial complex III deficiency, nuclear type 1, 124000 (3), Autosomal recessive"	Bcs1l (MGI:1914071)			
chr2	218663863	218672057	2q35	2q35		616014	"RNF25, AO7"	Ring finger protein 25	RNF25	64320	ENSG00000163481			Rnf25 (MGI:1890215)			
chr2	218672025	218702716	2q35	2q35		607652	"STK36, FU, KIAA1278"	Serine/threonine protein kinase 36	STK36	27148	ENSG00000163482			Stk36 (MGI:1920831)			
chr2	218781732	218815292	2q33-qter	2q35		606530	"CYP27A1, CYP27, CTX"	"Cytochrome P450, subfamily XXVIIA, polypeptide 1 (sterol 27-hydroxylase)"	CYP27A1	1593	ENSG00000135929		"Cerebrotendinous xanthomatosis, 213700 (3), Autosomal recessive"	Cyp27a1 (MGI:88594)			
chr2	218819948	218831802	2q35	2q35		604976	PRKAG3	"Protein kinase, AMP-activated, noncatalytic, gamma 3"	PRKAG3	53632	ENSG00000115592			Prkag3 (MGI:1891343)			
chr2	218859822	218874231	2q35	2q35		604663	WNT6	"Wingless-type MMTV integration site family, member 6"	WNT6	7475	ENSG00000115596			Wnt6 (MGI:98960)			
chr2	218874115	218893930	2q35	2q35		606268	"WNT10A, SSPS, STHAG4, OODD"	"Wingless-type MMTV integration site family, member 10A"	WNT10A	80326	ENSG00000135925		"Odontoonychodermal dysplasia, 257980 (3), Autosomal recessive; Schopf-Schulz-Passarge syndrome, 224750 (3), Autosomal recessive; Tooth agenesis, selective, 4, 150400 (3), Autosomal recessive, Autosomal dominant"	Wnt10a (MGI:108071)			
chr2	218959627	218962154	2q35	2q35		603764	"CDK5R2, NCK5AI"	"Cyclin-dependent kinase 5, regulatory subunit 2"	CDK5R2	8941	ENSG00000171450			Cdk5r2 (MGI:1330828)			
chr2	218981086	218985656	2q36	2q35		607150	FEV	Fifth Ewing sarcoma variant	FEV	54738	ENSG00000163497	fused with EWS in tumors		Fev (MGI:2449712)			
chr2	218990189	218993404	2q34-q36	2q35		600836	"CRYBA2, CTRCT42"	"Crystallin, beta A2"	CRYBA2	1412	ENSG00000163499	mutation identified in 1 CTRCT42 family	"?Cataract 42, 115900 (3), Autosomal dominant"	Cryba2 (MGI:104336)			
chr2	219001644	219001707	2q35	2q35		611173	"MIR375, MIRN375"	Micro RNA 375	MIR375	494324							
chr2	219002845	219043141	2q35	2q35		614270	"CFAP65, CCDC108"	Cilia- and flagella-associated protein 65	CFAP65	255101	ENSG00000181378			Cfap65 (MGI:2444274)			
chr2	219054419	219060515	2q33-q35	2q35		600726	"IHH, BDA1"	Indian hedgehog	IHH	3549	ENSG00000163501		"Acrocapitofemoral dysplasia, 607778 (3), Autosomal recessive; Brachydactyly, type A1, 112500 (3), Autosomal dominant"	Ihh (MGI:96533)			
chr2	219075323	219160864	2q35	2q35		611290	"NHEJ1, XLF"	Nonhomologous end-joining factor 1	NHEJ1	79840	ENSG00000187736		"Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, 611291 (3)"	Nhej1 (MGI:1922820)			
chr2	219206783	219209650	2q35	2q35		613474	"ZFAND2B, AIRAPL"	Zinc finger AN1 domain-containing protein 2B	ZFAND2B	130617	ENSG00000158552			Zfand2b (MGI:1916068)			
chr2	219209765	219219016	2q36	2q35		605452	"ABCB6, MTABC3, MCOPCB7, LAN, DUH3, PSHK2"	"ATP-binding cassette, subfamily B, member 6"	ABCB6	10058	ENSG00000115657		"[Blood group, Langereis system], 111600 (3); Dyschromatosis universalis hereditaria 3, 615402 (3), Autosomal dominant; Microphthalmia, isolated, with coloboma 7, 614497 (3), Autosomal dominant; Pseudohyperkalemia, familial, 2, due to red cell leak, 609153 (3), Autosomal dominant"	Abcb6 (MGI:1921354)			
chr2	219219379	219229687	2q35	2q35		612204	"ATG9A, APG9L1"	"Autophagy 9, S. cerevisiae, homolog of, A"	ATG9A	79065	ENSG00000198925			Atg9a (MGI:2138446)			
chr2	219229756	219236668	2q35	2q35		617541	"ANKZF1, ZNF744"	Ankyrin repeat- and zinc finger domain-containing 1	ANKZF1	55139	ENSG00000163516			Ankzf1 (MGI:1098746)			
chr2	219249710	219254607	2q35	2q35		191110	"TUBA4A, TUBA1, ALS22"	"Tubulin, alpha-4A"	TUBA4A	7277	ENSG00000127824		"Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia, 616208 (3), Autosomal dominant"	Tuba4a (MGI:1095410)			
chr2	219279317	219286899	2q35	2q35		604139	"DNAJB2, HSJ1, HSPF3, DSMA5"	"DnaJ, E. coli, homolog of, subfamily B, member 2 (heat-shock protein, DNAJ-like 1)"	DNAJB2	3300	ENSG00000135924		"Spinal muscular atrophy, distal, autosomal recessive, 5, 614881 (3), Autosomal recessive"	Dnajb2 (MGI:1928739)			
chr2	219289622	219309572	2q35-q36.1	2q35		601773	"PTPRN, IA2"	"Protein tyrosine phosphatase, receptor type N (islet cell antigen 2)"	PTPRN	5798	ENSG00000054356			Ptprn (MGI:102765)			
chr2	219327406	219334534	2q35	2q35		612721	RESP18	Regulated endocrine-specific protein 18	RESP18	389075	ENSG00000182698			Resp18 (MGI:1098222)			
chr2	219372028	219400021	2q35	2q35		611367	"DNPEP, ASPEP, DAP"	Aspartyl aminopeptidase	DNPEP	23549	ENSG00000123992			Dnpep (MGI:1278328)			
chr2	219418376	219426738	2q35	2q35		125660	"DES, CMD1I, MFM1, SCPNK, ARVD7, ARVC7, LGMD2R"	Desmin	DES	1674	ENSG00000175084	1 family with LGMD2R identified with mutation	"Cardiomyopathy, dilated, 1I, 604765 (3); ?Muscular dystrophy, limb-girdle, type 2R, 615325 (3), Autosomal recessive; Myopathy, myofibrillar, 1, 601419 (3), Autosomal recessive, Autosomal dominant; Scapuloperoneal syndrome, neurogenic, Kaeser type, 181400 (3), Autosomal dominant"	Des (MGI:94885)			
chr2	219434214	219493631	2q35	2q35		615950	"SPEG, APEG1, CNM5"	SPEG complex locus	SPEG	10290	ENSG00000072195		"Centronuclear myopathy 5, 615959 (3), Autosomal recessive"	Speg (MGI:109282)			
chr2	219498864	219506995	2q35	2q35		615495	"GMPPA, AAMR"	GDP-mannose pyrophosphorylase A	GMPPA	29926	ENSG00000144591		"Alacrima, achalasia, and mental retardation syndrome, 615510 (3), Autosomal recessive"	Gmppa (MGI:1916330)			
chr2	219514169	219538771	2q35-q36	2q35		606715	"ACCN4, ASIC4, BNAC4"	"Cation channel, amiloride-sensitive, neuronal, 4"	ASIC4	55515	ENSG00000072182			Asic4 (MGI:2652846)			
chr2	219538946	219543764	2q36.1	2q35		610405	"CHPF, CSS2"	Chondroitin polymerizing factor	CHPF	79586	ENSG00000123989			Chpf (MGI:106576)			
chr2	219549407	219571572	2q35	2q35		610991	"OBSL1, KIAA0657, 3M2"	Obscurin-like 1	OBSL1	23363	ENSG00000124006		"3-M syndrome 2, 612921 (3)"				
chr2	219572231	219575712	2q33-q36	2q35		147380	INHA	"Inhibin, alpha"	INHA	3623	ENSG00000123999	proximal to PAX3		Inha (MGI:96569)			
chr2	219597850	219616450	2q36	2q35		607172	"STK11IP, KIAA1898, LIP1"	Serine/threonine kinase 11 interacting protein	STK11IP	114790	ENSG00000144589			Stk11ip (MGI:1918978)			
chr2	219627569	219641979	2q36	2q35		106195	"SLC2C, AE3"	"Anion exchanger 3, neuronal"	SLC4A3	6508	ENSG00000114923			Slc4a3 (MGI:109350)			
chr2	220700000	230100000	2q36			102510	ACRPV	Acropectorovertebral dysplasia (F syndrome)		414058			"Acropectorovertebral dysplasia, 102510 (2), Autosomal dominant"				
chr2	220700000	230100000	2q36			613944	IGAN2	"IgA nephropathy, susceptibility to, 2"		100653384		between D2S1323 and D2S362	"{IgA nephropathy, susceptibility to, 2}, 613944 (2), ?Autosomal dominant"				
chr2	220700000	230100000	2q36.1-q36.3			613238	SPDA3	"Spondyloarthropathy, susceptibility to, 3"		100379218		max lod at D2S2228	"{Spondyloarthropathy, susceptibility to, 3}, 613238 (2)"				
chr2	221418026	221574201	2q36.1	2q36.1		602188	"EPHA4, HEK8, TYRO1"	Ephrin receptor EphA4	EPHA4	2043	ENSG00000116106			Epha4 (MGI:98277)			
chr2	222199886	222298995	2q36.1	2q36.1		606597	"PAX3, WS1, HUP2, CDHS, WS3"	Paired box homeotic gene-3	PAX3	5077	ENSG00000135903		"Craniofacial-deafness-hand syndrome, 122880 (3), Autosomal dominant; Rhabdomyosarcoma 2, alveolar, 268220 (3), Autosomal recessive; Waardenburg syndrome, type 1, 193500 (3), Autosomal dominant; Waardenburg syndrome, type 3, 148820 (3), Autosomal recessive, Autosomal dominant"	Pax3 (MGI:97487)			
chr2	222424051	222562621	2q36.1	2q36.1		612827	"SGPP2, SPP2"	Sphingosine-1-phosphate phosphatase 2	SGPP2	130367	ENSG00000163082			Sgpp2 (MGI:3589109)			
chr2	222571442	222656354	2q36	2q36.1		609690	"FARSLB, FRSB"	"Phenylalanine-tRNA synthetase-like, beta subunit"	FARSB	10056	ENSG00000116120			Farsb (MGI:1346035)			
chr2	222671737	222709929	2q36.1	2q36.1		610268	"MOGAT1, MGAT1, DGAT2L1"	Monoacylglycerol O-acyltransferase 1	MOGAT1	116255	ENSG00000124003			Mogat1 (MGI:1915643)			
chr2	222860933	222944650	2q34-q35	2q36.1		602371	"ACSL3, FACL3, ACS3"	Acyl-CoA synthetase long-chain family member 3	ACSL3	2181	ENSG00000123983			Acsl3 (MGI:1921455)			
chr2	223051929	223055636	2q35-q36	2q36.1		607775	"KCNE4, MIRP3"	"Potassium channel, voltage-gated, ISK-related subfamily, member 4"	KCNE4	23704	ENSG00000152049			Kcne4 (MGI:1891125)			
chr2	223596939	223602498	2q35-q36	2q36.1		118930	"SCG2, CHGC"	Secretogranin II (chromogranin C)	SCG2	7857	ENSG00000171951			Scg2 (MGI:103033)			
chr2	223755329	223837601	2q36.1	2q36.1		615781	"AP1S3, PSORS15"	"Adaptor-related protein complex 1, sigma-3 subunit"	AP1S3	130340	ENSG00000152056		"{Psoriasis 15, pustular, susceptibility to}, 616106 (3), Autosomal dominant"	Ap1s3 (MGI:1891304)			
chr2	223950845	223967713	2q36	2q36.1		611849	"MRPL44, COXPD16"	Mitochondrial ribosomal protein L44	MRPL44	65080	ENSG00000135900	Mutation identified in 1 family	"?Combined oxidative phosphorylation deficiency 16, 615395 (3), Autosomal recessive"	Mrpl44 (MGI:1916413)			
chr2	223975047	224039318	2q33-q35	2q36.1		177010	"PI7, PN1, SERPINE2"	Protease inhibitor 7 (protease nexin I)	SERPINE2	5270	ENSG00000135919	near MYL1; ?COPD susceptibility		Serpine2 (MGI:101780)			
chr2	224300000	225200000	2q36.2			613658	RJBS	Rajab syndrome		100528027		between D2S351 and D2S2390	"Rajab syndrome, 613658 (2), Autosomal recessive"				
chr2	224470149	224585396	2q36	2q36.2		603136	"CUL3, PHA2E"	Cullin 3	CUL3	8452	ENSG00000036257		"Pseudohypoaldosteronism, type IIE, 614496 (3), Autosomal dominant"	Cul3 (MGI:1347360)			
chr2	224765089	225042688	2q36.2	2q36.2		611518	"DOCK10, KIAA0694, ZIZ3"	Dedicator of cytokinesis 10	DOCK10	55619	ENSG00000135905			Dock10 (MGI:2146320)			
chr2	225399709	225703652	2q36.3	2q36.3		615478	"NYPA2, KIAA1486"	Neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 2	NYAP2	57624	ENSG00000144460			Nyap2 (MGI:2443135)			
chr2	226731316	226798789	2q36	2q36.3		147545	IRS1	Insulin receptor substrate-1	IRS1	3667	ENSG00000169047		"{Coronary artery disease, susceptibility to} (3); {Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant"	Irs1 (MGI:99454)			
chr2	226800158	226999209	2q36.3	2q36.3		617515	"RHBDD1, RRP4, RHBDL4"	Rhomboid domain-containing 1	RHBDD1	84236	ENSG00000144468			Rhbdd1 (MGI:1924117)			
chr2	226970292	227164558	2q36-q37	2q36.3		120131	COL4A4	"Collagen IV, alpha-4 polypeptide"	COL4A4	1286	ENSG00000081052	head-to-head with COL4A4 in same YAC	"Alport syndrome, autosomal recessive, 203780 (3), Autosomal recessive; Hematuria, familial benign (3)"	Col4a4 (MGI:104687)			
chr2	227164564	227314791	2q36-q37	2q36.3		120070	COL4A3	"Collagen IV, alpha-3 polypeptide (Goodpasture antigen)"	COL4A3	1285	ENSG00000169031	noncollagenous domain = Goodpasture antigen	"Alport syndrome, autosomal dominant, 104200 (3), Autosomal dominant; Alport syndrome, autosomal recessive, 203780 (3), Autosomal recessive; Hematuria, benign familial, 141200 (3), Autosomal dominant"	Col4a3 (MGI:104688)			
chr2	227325150	227357835	2q36.3	2q36.3		614785	"MFF, C2orf33, EMPF2"	Mitochondrial fission factor	MFF	56947	ENSG00000168958		"Encephalopathy due to defective mitochondrial and peroxisomal fission 2, 617086 (3), Autosomal recessive"				
chr2	227362037	227379305	2q36.3	2q36.3		615404	"TM4SF20, SLI5"	"Transmembrane 4 L6 family, member 20"	TM4SF20	79853	ENSG00000168955		"{Specific language impairment 5}, 615432 (3), Autosomal dominant"	Tm4sf20 (MGI:1913511)			
chr2	227472168	227561221	2q36	2q36.3		600862	"AGFG1, HRB, RIP, RAB"	ADP-ribosylation factor GTPase-activating protein with FG repeats 1	AGFG1	3267	ENSG00000173744			Agfg1 (MGI:1333754)			
chr2	227685209	227718029	2q36.3	2q36.3		606152	"SLC19A3, THMD2, BBGD"	"Solute carrier family 19 (folate transporter), member 3"	SLC19A3	80704	ENSG00000135917		"Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 (3), Autosomal recessive"	Slc19a3 (MGI:1931307)			
chr2	227813841	227817563	2q33-q37	2q36.3		601960	"CCL20, SCYA20, MIP3A, LARC"	"Chemokine, C-C motif, ligand 20"	CCL20	6364	ENSG00000115009			Ccl20 (MGI:1329031)			
chr2	227979953	228181998	2q36	2q36.3		611646	"SPHKAP, SKIP, KIAA1678"	"SPHK1 interactor, AKAP domain containing"	SPHKAP	80309	ENSG00000153820			Sphkap (MGI:1924879)			
chr2	229023972	229271340	2q36.3	2q36.3		612930	"PID1, NYGGF4"	Phosphotyrosine interaction domain-containing 1	PID1	55022	ENSG00000153823			Pid1 (MGI:2138391)			
chr2	229357628	229714569	2q37	2q36.3		607299	DNER	Delta-and notch-like egf-related receptor	DNER	92737	ENSG00000187957			Dner (MGI:2152889)			
chr2	229763836	229923233	2q36.3	2q36.3		604506	"TRIP12, MRD49"	Thyroid hormone receptor interactor 12	TRIP12	9320	ENSG00000153827		"Mental retardation, autosomal dominant 49, 617752 (3), Autosomal dominant"	Trip12 (MGI:1309481)			
chr2	229922490	230013912	2q37.1	2q36.3		609105	"FBXO36, FBX36"	F-box only protein 36	FBXO36	130888	ENSG00000153832			Fbxo36 (MGI:1289192)			
chr2	230100000	242193529	2q37			600430	"BDMR, C2DELq37, DEL2q37"	Chromosome 2q37 deletion syndrome					"Chromosome 2q37 deletion syndrome, 600430 (4), Autosomal dominant"				
chr2	230100000	242193529	2q37.1-q37.3			605934	HPE6	Holoprosencephaly 6		117190			"Holoprosencephaly 6, 605934 (2)"				
chr2	230100000	242193529	2q37			606656	IBGC2	"Basal ganglia calcification, idiopathic, 2"		100874532			"Basal ganglia calcification, idiopathic, 2, 606656 (2)"				
chr2	230100000	234700000	2q37.1			609995	MYP12	Myopia 12	MYP12	664780		max lod at D2S2344	"Myopia 12, 609995 (2)"				
chr2	230100000	234700000	2q37.1			613440	STQTL21	Stature quantitative trait locus 21		100502568		associated with rs6717918	"{Stature QTL 21}, 613440 (2)"				
chr2	230165472	230225728	2q37.1	2q37.1		604457	"SP110, IFI41, IFI75, VODI"	"SP110 nuclear body protein (interferon-induced protein 41, 30kD; interferon-induced protein 75, 52kD)"	SP110	3431	ENSG00000135899		"Hepatic venoocclusive disease with immunodeficiency, 235550 (3), Autosomal recessive; {Mycobacterium tuberculosis, susceptibility to}, 607948 (3)"	"Sp110,Gm15753,Gm16026 (MGI:3783243,MGI:1923364,MGI:3783195)"			
chr2	230327151	230407505	2q37.1	2q37.1		617747	SP140L	Nuclear body protein SP140-like	SP140L	93349	ENSG00000185404						
chr2	230416155	230545601	2q37.1	2q37.1		604585	SP100	Nuclear antigen SP100	SP100	6672	ENSG00000067066						
chr2	230712841	230821074	2q37.1	2q37.1		612174	CAB39	Calcium-binding protein 39	CAB39	51719	ENSG00000135932			Cab39 (MGI:107438)			
chr2	230864597	230879253	2q37	2q37.1		609554	"ITM2C, BRI3"	Integral membrane protein 2C	ITM2C	81618	ENSG00000135916			Itm2c (MGI:1927594)			
chr2	230907317	230961269	2q37	2q37.1		604107	GPR55	G protein-coupled receptor 55	GPR55	9290	ENSG00000135898			Gpr55 (MGI:2685064)			
chr2	231056863	231172826	2q37.1	2q37.1		617842	PSMD1	"Proteasome 26S subunit, non-ATPase, 1"	PSMD1	5707	ENSG00000173692			Psmd1 (MGI:1917497)			
chr2	231108229	231126171	2q36.3-q37.1	2q37.1		601122	HTR2B	5-hydroxytryptamine (serotonin) receptor-2B	HTR2B	3357	ENSG00000135914			Htr2b (MGI:109323)			
chr2	231198545	231394990	2q37.1	2q37.1		617612	"ARMC9, KIAA1868, JBTS30"	Armadillo repeat-containing protein 9	ARMC9	80210	ENSG00000135931		"Joubert syndrome 30, 617622 (3), Autosomal recessive"	Armc9 (MGI:1926045)			
chr2	231395623	231401163	2q37.1	2q37.1		615313	B3GNT7	"Beta-1,3-N-acetylglucosaminyltransferase 7"	B3GNT7	93010	ENSG00000156966			B3gnt7 (MGI:2384394)			
chr2	231454747	231464493	2q12-qter	2q37.1		164035	NCL	Nucleolin	NCL	4691	ENSG00000115053			Ncl (MGI:97286)			
chr2	231460367	231460441	2q12-qter	2q37.1		611133	"SNORD82, RNU82"	"Small nucleolar RNA, C/D box, 82"	SNORD82	25826							
chr2	231519902	231530470	2q37.1	2q37.1		604153	"NMUR1, GPR66, FM3"	Neuromedin U receptor 1	NMUR1	10316	ENSG00000171596			Nmur1 (MGI:1341898)			
chr2	231708524	231713540	2q36-q37	2q37.1		188390	"PTMA, TMSA"	"Prothymosin, alpha (gene sequence 28)"	PTMA	5757	ENSG00000187514						
chr2	231732424	231781326	2q36-q37	2q37.1		602676	"PDE6D, JBTS22"	"Phosphodiesterase 6D, cGMP-specific, rod, delta"	PDE6D	5147	ENSG00000156973	mutation identified in 1 JBTS22 family	"?Joubert syndrome 22, 615665 (3), Autosomal recessive"	Pde6d (MGI:1270843)			
chr2	231781670	231809252	2q37.1	2q37.1		616010	COPS7B	"COP9 signalosome, subunit 7B"	COPS7B	64708	ENSG00000144524			Cops7b (MGI:1349388)			
chr2	231922093	231926404	2q24-qter	2q37.1		600296	NPPC	Natriuretic peptide precursor C	NPPC	4880	ENSG00000163273			Nppc (MGI:97369)			
chr2	231961582	232343967	2q37.2	2q37.1		614184	"DIS3L2, PRLMNS"	"Dis3 mitotic control, S. cerevisiae, homolog-like 2"	DIS3L2	129563	ENSG00000144535		"Perlman syndrome, 267000 (3), Autosomal recessive"	Dis3l2 (MGI:2442555)			
chr2	232378533	232382888	2q37	2q37.1		171800	ALPP	"Alkaline phosphatase, placental (Regan isozyme)"	ALPP	250	ENSG00000163283			Alpi (MGI:1924018)			
chr2	232406841	232410713	2q37	2q37.1		171810	ALPPL2	"Alkaline phosphatase, placental-like 2"	ALPPL2	251	ENSG00000163286			Alppl2 (MGI:108009)			
chr2	232456111	232460744	2q37.1	2q37.1		171740	ALPI	"Alkaline phosphatase, intestinal"	ALPI	248	ENSG00000163295	close to ALPP; proximal to PAX3		Akp3 (MGI:87984)			
chr2	232479826	232487858	2q36-q37	2q37.1		605896	"ECEL1, XCE, DA5D"	Endothelin-converting enzyme-like 1	ECEL1	9427	ENSG00000171551		"Arthrogryposis, distal, type 5D, 615065 (3), Autosomal recessive"	Ecel1 (MGI:1343461)			
chr2	232520462	232525715	2q37.1	2q37.1		613858	"PRSS56, MCOP6"	"Protease, serine, 56"	PRSS56	646960	ENSG00000237412		"Microphthalmia, isolated 6, 613517 (3), Autosomal recessive"	Prss56 (MGI:1916703)			
chr2	232526159	232537906	2q33-q34	2q37.1		100720	"CHRND, ACHRD, SCCMS, CMS3A, CMS3B, CMS3C"	"Cholinergic receptor, nicotinic, delta polypeptide"	CHRND	1144	ENSG00000135902	mutation identified in 1 CMS3A patient and 1 CMS3C family	"Multiple pterygium syndrome, lethal type, 253290 (3), Autosomal recessive; ?Myasthenic syndrome, congenital, 3A, slow-channel, 616321 (3), Autosomal dominant; Myasthenic syndrome, congenital, 3B, fast-channel, 616322 (3), Autosomal recessive; ?Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency, 616323 (3), Autosomal recessive"	Chrnd (MGI:87893)			
chr2	232539726	232546327	2q33-q34	2q37.1		100730	"CHRNG, ACHRG"	"Cholinergic receptor, nicotinic, gamma polypeptide"	CHRNG	1146	ENSG00000196811	tightly linked to CHRND by RE	"Escobar syndrome, 265000 (3), Autosomal recessive; Multiple pterygium syndrome, lethal type, 253290 (3), Autosomal recessive"	Chrng (MGI:87895)			
chr2	232547969	232550589	2q37.1	2q37.1		612972	TIGD1	TIGGER transposable element-derived gene 1	TIGD1	200765	ENSG00000221944						
chr2	232550586	232583644	2q37.1	2q37.1		605895	"EIF4E2, EIF4EL3, 4EHP"	"Eukaryotic translation initiation factor 4E family, member 2"	EIF4E2	9470	ENSG00000135930			Eif4e2 (MGI:1914440)			
chr2	232606056	232682780	2q37.1	2q37.1		611617	EFHD1	"EF-hand domain family, member D1"	EFHD1	80303	ENSG00000115468			Efhd1 (MGI:1921607)			
chr2	232697304	232860576	2q37.1	2q37.1		612003	"GIGYF2, KIAA0642, PARK11"	GRB10-interacting GYF protein 2	GIGYF2	26058	ENSG00000204120		"{Parkinson disease 11}, 607688 (3)"	Gigyf2 (MGI:2138584)			
chr2	232765801	232776564	2q37	2q37.1		603208	"KCNJ13, SVD, LCA16"	"Potassium inwardly-rectifying channel, subfamily J, member 13"	KCNJ13	3769	ENSG00000115474		"Leber congenital amaurosis 16, 614186 (3), Autosomal recessive; Snowflake vitreoretinal degeneration, 193230 (3), Autosomal dominant"	Kcnj13 (MGI:3781032)			
chr2	232878685	233013240	2q37	2q37.1		605991	NGEF	Neuronal guanine nucleotide exchange factor	NGEF	25791	ENSG00000066248			Ngef (MGI:1858414)			
chr2	233032671	233035056	2q37	2q37.1		605528	"NEU2, SIAL2"	Neuraminidase 2	NEU2	4759	ENSG00000115488			Neu2 (MGI:1344417)			
chr2	233059966	233207902	2q36-q37	2q37.1		601582	"INPP5D, SHIP"	"Inositol polyphosphate-5-phosphatase, 145kD"	INPP5D	3635	ENSG00000168918			Inpp5d (MGI:107357)			
chr2	233251570	233295673	2q37.1	2q37.1		610767	"ATG16L1, APG16L, IBD10"	Autophagy 16-like 1	ATG16L1	55054	ENSG00000085978		"{Inflammatory bowel disease (Crohn disease) 10}, 611081 (3)"	Atg16l1 (MGI:1924290)			
chr2	233275725	233276002	2q37.1	2q37.1		615640	SCARNA5	Small Cajal body-specific RNA 5	SCARNA5	677775		within intron 9 of ATG16L1					
chr2	233288675	233288940	2q37.1	2q37.1		615641	SCARNA6	Small Cajal body-specific RNA 6	SCARNA6	677772		within intron 12 of ATG16L1					
chr2	233307662	233347065	2q37.1	2q37.1		181031	"SAG, RP47"	S-antigen; retina and pineal gland (arrestin)	SAG	6295	ENSG00000130561		"Oguchi disease-1, 258100 (3), Autosomal recessive; Retinitis pigmentosa 47, 613758 (3)"	Sag (MGI:98227)			
chr2	233354506	233472097	2q37.1	2q37.1		601826	DGKD	"Diacylglycerol kinase, delta, 130kD"	DGKD	8527	ENSG00000077044			Dgkd (MGI:2138334)			
chr2	233475518	233566788	2q37.1	2q37.1		610570	USP40	Ubiquitin-specific protease 40	USP40	55230	ENSG00000085982			Usp40 (MGI:2443184)			
chr2	233617644	233773298	2q37	2q37.1		606433	UGT1A8	"UDP-glycosyltransferase 1 family, polypeptide A8"	UGT1A8	54576	ENSG00000242366			"Ugt1a9,Ugt1a10 (MGI:3576092,MGI:3580642)"			
chr2	233636476	233773304	2q37	2q37.1		606435	UGT1A10	"UDP-glycosyltransferase 1 family, polypeptide A10"	UGT1A10	54575	ENSG00000242515			"Ugt1a9,Ugt1a10 (MGI:3576092,MGI:3580642)"			
chr2	233671897	233773304	2q37	2q37.1		606434	UGT1A9	"UDP-glycosyltransferase 1 family, polypeptide A9"	UGT1A9	54600	ENSG00000241119			"Ugt1a9,Ugt1a10 (MGI:3576092,MGI:3580642)"			
chr2	233681937	233773298	2q37	2q37.1		606432	UGT1A7	"UDP-glycosyltransferase 1 family, polypeptide A7"	UGT1A7	54577	ENSG00000244122			"Ugt1a9,Ugt1a10 (MGI:3576092,MGI:3580642)"			
chr2	233691674	233773304	2q37	2q37.1		606431	UGT1A6	"UDP-glycosyltransferase 1 family, polypeptide A6"	UGT1A6	54578	ENSG00000167165			"Ugt1a6b,Ugt1a6a (MGI:3580629,MGI:2137698)"			
chr2	233712991	233773298	2q37	2q37.1		606430	UGT1A5	"UDP-glycosyltransferase 1 family, polypeptide A5"	UGT1A5	54579	ENSG00000240224						
chr2	233718791	233773298	2q37	2q37.1		606429	"UGT1A4, UGT1D"	"UDP-glycosyltransferase 1 family, polypeptide A4"	UGT1A4	54657	ENSG00000244474			Ugt1a5 (MGI:3032634)			
chr2	233729126	233773298	2q37	2q37.1		606428	"UGT1A3, UGT1C"	"UDP-glycosyltransferase 1 family, polypeptide A3"	UGT1A3	54659	ENSG00000243135			Ugt1a2 (MGI:3576049)			
chr2	233760272	233773298	2q37	2q37.1		191740	"UGT1A1, UGT1, GNT1, BILIQTL1"	"UDP glycosyltransferase 1 family, polypeptide A1"	UGT1A1	54658	ENSG00000241635		"[Bilirubin, serum level of, QTL1], 601816 (3); Crigler-Najjar syndrome, type I, 218800 (3), Autosomal recessive; Crigler-Najjar syndrome, type II, 606785 (3), Autosomal recessive; [Gilbert syndrome], 143500 (3), Autosomal recessive; Hyperbilirubinemia, familial transient neonatal, 237900 (3), Autosomal recessive"	Ugt1a1 (MGI:98898)			
chr2	233836700	233854565	2q37.1	2q37.1		612667	HJURP	Holliday junction recognition protein	HJURP	55355	ENSG00000123485			Hjurp (MGI:2685821)			
chr2	233917341	234019521	2q37	2q37.1		606678	"TRPM8, TRPP8"	"Transient receptor potential cation channel, subfamily M, member 8"	TRPM8	79054	ENSG00000144481			Trpm8 (MGI:2181435)			
chr2	234050666	234077133	2q37-qter	2q37.1		602637	SPP2	"Secreted phosphoprotein-2, 24kD"	SPP2	6694	ENSG00000072080			Spp2 (MGI:1922646)			
chr2	234493040	234497052	2q37.1	2q37.1		604787	"ARL4C, ARL7"	ADP-ribosylation factor-like 4C	ARL4C	10123	ENSG00000188042			Arl4c (MGI:2445172)			
chr2	234951983	235055713	2q37.1-q37.2	2q37.2		605611	"SH3BP4, BOG25"	SH3 domain-binding protein 4	SH3BP4	23677	ENSG00000130147			Sh3bp4 (MGI:2138297)			
chr2	236165235	236168008	2q36-q37	2q37.2		601135	GBX2	Gastrulation brain homeobox 2	GBX2	2637	ENSG00000168505			Gbx2 (MGI:95668)			
chr2	236537130	236582357	2q37	2q37.3		610376	"ACKR3, CXCR7, CMKOR1, GPR159, RDC1"	Atypical chemokine receptor 3	ACKR3	57007	ENSG00000144476			Ackr3 (MGI:109562)			
chr2	237085440	237098845	2q37.3	2q37.3		616011	"COPS8, CSN8"	"COP9 signalosome, subunit 8"	COPS8	10920	ENSG00000198612			Cops8 (MGI:1915363)			
chr2	237324011	237434821	2q37	2q37.3		120250	"COL6A3, DYT27, BTHLM1, UCMD1"	"Collagen VI, alpha-3 polypeptide"	COL6A3	1293	ENSG00000163359	close to CRBP1	"Bethlem myopathy 1, 158810 (3), Autosomal recessive, Autosomal dominant; Dystonia 27, 616411 (3), Autosomal recessive; Ullrich congenital muscular dystrophy 1, 254090 (3), Autosomal recessive, Autosomal dominant"	Col6a3 (MGI:88461)			
chr2	237486409	237555317	2q37	2q37.3		606526	MLPH	Melanophilin	MLPH	79083	ENSG00000115648		"Griscelli syndrome, type 3, 609227 (3), Autosomal recessive"	Mlph (MGI:2176380)			
chr2	237566573	237567174	2q37.3	2q37.3		602663	"PRLH, PRRP"	Prolactin-releasing hormone	PRLH	51052	ENSG00000071677			Prlh (MGI:3644668)			
chr2	237574321	237591125	2q37.3	2q37.3		602206	RAB17	Ras-associated protein	RAB17	64284	ENSG00000124839			Rab17 (MGI:104640)			
chr2	237627575	237781646	2q37.3	2q37.3		603256	"LRRFIP1, GCF2, TRIP, FLAP1"	Leucine-rich repeat in FLII-interacting protein 1	LRRFIP1	9208	ENSG00000124831			Lrrfip1 (MGI:1342770)			
chr2	237858554	237912116	2q36-q37.1	2q37.3		605153	RAMP1	Receptor activity-modifying protein 1	RAMP1	10267	ENSG00000132329			Ramp1 (MGI:1858418)			
chr2	237966944	238042781	2q37.3	2q37.3		617700	"UBE2F, NCE2"	Ubiquitin-conjugating enzyme E2F	UBE2F	140739	ENSG00000184182			Ube2f (MGI:1915171)			
chr2	238060923	238099412	2q37.3	2q37.3		611056	"SCLY, SCL"	Selenocysteine lyase	SCLY	51540	ENSG00000132330			Scly (MGI:1355310)			
chr2	238159007	238168889	2q37.3	2q37.3		615099	"ERFE, FAM132B, CTRP15"	Erythroferrone	ERFE	151176	ENSG00000178752			Erfe (MGI:3606476)			
chr2	238238266	238240123	2q37.3	2q37.3		610331	HES6	"Hairy/enhancer of split, Drosophila, homolog of, 6"	HES6	55502	ENSG00000144485			Hes6 (MGI:1859852)			
chr2	238244037	238290101	2q37.3	2q37.3		603426	"PER2, FASPS1, KIAA0347"	"Period, Drosophila, homolog of, 2"	PER2	8864	ENSG00000132326		"Advanced sleep phase syndrome, familial, 1, 604348 (3), Autosomal dominant"	Per2 (MGI:1195265)			
chr2	238320488	238400899	2q37.3	2q37.3		607380	"TRAF3IP1, MIPT3, SLSN9"	TNF receptor-associated factor 3-interacting protein 1	TRAF3IP1	26146	ENSG00000204104		"Senior-Loken syndrome 9, 616629 (3), Autosomal recessive"	Traf3ip1 (MGI:1921269)			
chr2	238426927	238452249	2q37	2q37.3		605758	ASB1	Ankyrin repeat-containing SOCS box protein 1	ASB1	51665	ENSG00000065802			Asb1 (MGI:1929735)			
chr2	238848031	238910547	2q37.3	2q37.3		607556	"TWIST2, DERMO1, SETLSS, FFDD3, BBRSAY, AMS"	"Twist, Drosophila, homolog of, 2 (dermis-expressed protein 1, mouse, homolog of)"	TWIST2	117581	ENSG00000233608		"Ablepharon-macrostomia syndrome, 200110 (3), Autosomal dominant; Barber-Say syndrome, 209885 (3), Autosomal dominant; Focal facial dermal dysplasia 3, Setleis type, 227260 (3), Autosomal recessive"	Twist2 (MGI:104685)			
chr2	239048167	239401646	2q37.2	2q37.3		605314	"HDAC4, HDACA"	Histone deacetylase 4	HDAC4	9759	ENSG00000068024			Hdac4 (MGI:3036234)			
chr2	239892449	240025401	2q37.3	2q37.3		603835	NDUFA10	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 10"	NDUFA10	4705	ENSG00000130414		"Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufa10 (MGI:1914523)			
chr2	240138941	240141372	2q37.3	2q37.3		607877	OTOSP	Otospiralin	OTOS	150677	ENSG00000178602			Otos (MGI:2672814)			
chr2	240435697	240468077	2q35-q37	2q37.3		600395	GPC1	Glypican 1	GPC1	2817	ENSG00000063660			Gpc1 (MGI:1194891)			
chr2	240456000	240456088	2q37.3	2q37.3		615209	MIR149	Micro RNA 149	MIR149	406941							
chr2	240568525	240578731	2q37.3	2q37.3		605287	RNPEPL1	Arginyl aminopeptidase-like 1 (aminopeptidase B-like)	RNPEPL1	57140	ENSG00000142327			Rnpepl1 (MGI:1914170)			
chr2	240586715	240599108	2q37.3	2q37.3		605286	"CAPN10, NIDDM1"	Calpain-10	CAPN10	11132	ENSG00000142330		"{Diabetes mellitus, noninsulin-dependent 1}, 601283 (3)"	Capn10 (MGI:1344392)			
chr2	240605407	240631258	2q37.3	2q37.3		602646	GPR35	G protein-coupled receptor-35	GPR35	2859	ENSG00000178623			Gpr35 (MGI:1929509)			
chr2	240691844	240698482	2q34-q37	2q37.3		609789	"AQP12A, AQPX2, AQP12"	Aquaporin 12A	AQP12A	375318	ENSG00000184945			Aqp12 (MGI:2664636)			
chr2	240713763	240820307	2q37	2q37.3		601255	"KIF1A, ATSV, UNC104, SPG30, HSN2C, MRD9"	Kinesin family member 1A	KIF1A	547	ENSG00000130294	incorrectly assigned to chr.9	"Mental retardation, autosomal dominant 9, 614255 (3), Autosomal dominant; Neuropathy, hereditary sensory, type IIC, 614213 (3), Autosomal recessive; Spastic paraplegia 30, autosomal recessive, 610357 (3), Autosomal recessive"	Kif1a (MGI:108391)			
chr2	240868744	240879118	2q36-q37	2q37.3		604285	"AGXT, SPAT"	"Alanine-glyoxylate aminotransferase, liver-specific peroxisomal"	AGXT	189	ENSG00000172482		"Hyperoxaluria, primary, type 1, 259900 (3), Autosomal recessive"	Agxt (MGI:1329033)			
chr2	240997409	241095567	2q37.3	2q37.3		616634	"SNED1, SNEP"	"SUSHI, NIDOGEN, and EGF-like domains protein 1"	SNED1	25992	ENSG00000162804			Sned1 (MGI:3045960)			
chr2	241074393	241102331	2q37.3	2q37.3		615393	"MTERF4, MTERFD2"	Mitochondrial transcription termination factor 4	MTERF4	130916	ENSG00000122085			Mterf4 (MGI:1918355)			
chr2	241106098	241150263	2q37.3	2q37.3		607505	"PASK, KIAA0135"	Pas domain-containing serine-threonine kinase	PASK	23178	ENSG00000115687			Pask (MGI:2155936)			
chr2	241149572	241183649	2q37.3	2q37.3		602877	"PPP1R7, SDS22"	"Protein phosphatase 1, regulatory subunit 7"	PPP1R7	5510	ENSG00000115685			Ppp1r7 (MGI:1913635)			
chr2	241188508	241239601	2q37.3	2q37.3		605096	"TMEM16G, PCANAP5, IPCA5, DTMPP, NGEP"	Transmembrane protein 16G	ANO7	50636	ENSG00000146205			Ano7 (MGI:3052714)			
chr2	241227263	241315841	2q37	2q37.3		142695	"HDLBP, VGL"	High-density lipoprotein-binding protein	HDLBP	3069	ENSG00000115677			Hdlbp (MGI:99256)			
chr2	241315186	241354026	2q37	2q37.3		601506	"SEPT2, NEDD5, DIFF6"	Septin 2	2-Sep	4735	ENSG00000168385			Sept2 (MGI:97298)			
chr2	241356248	241494841	2q37.3	2q37.3		617586	"FARP2, FRG, FIR"	"FERM, ARHGEF, and pleckstrin domain-containing protein 2"	FARP2	9855	ENSG00000006607			Farp2 (MGI:2385126)			
chr2	241494706	241509729	2q37.3	2q37.3		602255	"STK25, SOK1, YSK1"	Serine/threonine protein kinase 25	STK25	10494	ENSG00000115694			Stk25 (MGI:1891699)			
chr2	241558730	241574137	2q37.3	2q37.3		605404	"BOK, BCL2L9"	BCL2-related ovarian killer	BOK	666	ENSG00000176720			Bok (MGI:1858494)			
chr2	241584404	241637542	2q37.3	2q37.3		612533	THAP4	THAP domain-containing protein 4	THAP4	51078	ENSG00000176946			Thap4 (MGI:1914276)			
chr2	241637611	241673856	2q37.3	2q37.3		611338	"ATG4B, APG4B, KIAA0943"	"Autophagy 4, S. cerevisiae, homolog of, B"	ATG4B	23192	ENSG00000168397			Atg4b (MGI:1913865)			
chr2	241675741	241686967	2q37.3	2q37.3		188345	"DTYMK, TYMK, CDC8"	Deoxythymidylate kinase	DTYMK	1841	ENSG00000168393			Dtymk (MGI:108396)			
chr2	241687011	241729480	2q37.3	2q37.3		608525	ING5	Inhibitor of growth-5	ING5	84289	ENSG00000168395			Ing5 (MGI:1922816)			
chr2	241734578	241768815	2q37.3	2q37.3		609186	"D2HGDH, D2HGD"	D-2-hydroxyglutarate dehydrogenase	D2HGDH	728294	ENSG00000180902		"D-2-hydroxyglutaric aciduria, 600721 (3), Autosomal recessive"	D2hgdh (MGI:2138209)			
chr2	241776824	241804286	2q37.3	2q37.3		608237	"GAL3ST2, GP3ST"	Galactose-3-O-sulfotransferase 2	GAL3ST2	64090	ENSG00000154252			"Gal3st2,Gal3st2c,Gal3st2b (MGI:2685834,MGI:3646771,MGI:3711964)"			
chr2	241809064	241817412	2q37.3	2q37.3		608527	NEU4	Neuraminidase 4	NEU4	129807	ENSG00000204099			Neu4 (MGI:2661364)			
chr2	241849880	241858907	2q37.3	2q37.3		600244	"PDCD1, SLEB2"	Programmed cell death 1	PDCD1	5133	ENSG00000188389		"{Multiple sclerosis, disease progression, modifier of}, 126200 (3), Multifactorial; {Systemic lupus erythematosus, susceptibility to, 2}, 605218 (3)"	Pdcd1 (MGI:104879)			
chr2	0	242193529	Chr.2			601136	TSE2	Transsuppressor of expression 2		57324							
chr3	0	90900000	3p			607135	CRCL	Creatinine clearance QTL		261727		in African Americans	"Creatinine clearance QTL, 607135 (2)"				
chr3	0	16300000	3pter-p25			613792	"DEL3pterp25, C3DELpterp25"	3p- syndrome (chromosome 3pter-p25 deletion syndrome)				contiguous gene deletion syndrome	"3p- syndrome, 613792 (4), Autosomal dominant"				
chr3	0	8100000	3p26			609299	HPC5	"Prostate cancer, hereditary, 5"		619402		between D3S1270 and D3S4559	"{Prostate cancer, hereditary, 5}, 176807 (2), Autosomal dominant"				
chr3	0	8100000	3p26			608448	IBD9	Inflammatory bowel disease 9	IBD9	317669			"{Inflammatory bowel disease 9}, 608448 (2)"				
chr3	0	26300000	3p26-p24.2			252350	"MYMY1, MYMY"	Moyamoya disease	MYMY1	50960		max lod at D3S3050	"Moyamoya disease, 252350 (2), Autosomal recessive"				
chr3	0	8100000	3p26			608982	STQTL5	Stature quantitative trait locus 5		619479		max lod between D3S1297 and D3S1304	"{Stature QTL 5}, 608982 (2)"				
chr3	196587	409416	3p26.1	3p26.3		607416	"CHL1, CALL, L1CAM2"	"CHL1, mouse, homolog of (L1 cell adhesion molecule 2)"	CHL1	10752	ENSG00000134121			Chl1 (MGI:1098266)			
chr3	978020	1403609	3p26-p25	3p26.3		607220	"CNTN6, NB3"	Contactin 6	CNTN6	27255	ENSG00000134115			Cntn6 (MGI:1858223)			
chr3	2098802	3059079	3p26-p25	3p26.3-p26.2		607280	CNTN4	Contactin 4	CNTN4	152330	ENSG00000144619			Cntn4 (MGI:1095737)			
chr3	3066323	3110413	3p26-p24	3p26.2		147851	IL5RA	"Interleukin-5 receptor, alpha"	IL5RA	3568	ENSG00000091181			Il5ra (MGI:96558)			
chr3	3126915	3153434	3p25.1	3p26.2		612907	"TRNT1, SIFD, RPEM"	"tRNA nucleotidyltransferase, CCA-adding, 1"	TRNT1	51095	ENSG00000072756	pseudogenes on chromosomes 1 and 22	"Retinitis pigmentosa and erythrocytic microcytosis, 616959 (3), Autosomal recessive; Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay, 616084 (3), Autosomal recessive"	Trnt1 (MGI:1917297)			
chr3	3148489	3179716	3p26.2	3p26.2		609262	"CRBN, MRT2"	Cereblon	CRBN	51185	ENSG00000113851	between D3S3525 and D3S1560	"Mental retardation, autosomal recessive 2, 607417 (3), Autosomal recessive"	Crbn (MGI:1913277)			
chr3	4000000	16300000	3p26.1-p25.1			612976	ARHI2	Age-related hearing impairment 2		100302721		"associated with rs11928865, rs779701, and rs779706"	"{Age-related hearing impairment 2}, 612976 (2)"				
chr3	4034713	4467281	3p26	3p26.1		607939	"SUMF1, FGE"	Sulfatase-modifying factor-1	SUMF1	285362	ENSG00000144455		"Multiple sulfatase deficiency, 272200 (3), Autosomal recessive"	Sumf1 (MGI:1889844)			
chr3	4303303	4320648	3p26	3p26.1		609834	"SETMAR, METNASE"	SET and Mariner transposase domains-containing protein	SETMAR	6419	ENSG00000170364						
chr3	4493347	4847839	3p26.1	3p26.1		147265	"ITPR1, SCA15, SCA16, SCA29"	"Inositol 1,4,5-triphosphate receptor, type 1"	ITPR1	3708	ENSG00000150995		"Gillespie syndrome, 206700 (3), Autosomal recessive, Autosomal dominant; Spinocerebellar ataxia 15, 606658 (3), Autosomal dominant; Spinocerebellar ataxia 29, congenital nonprogressive, 117360 (3), Autosomal dominant"	Itpr1 (MGI:96623)			
chr3	4749191	4751589	3p26.2	3p26.1		611662	EGO	Eosinophil granule ontogeny	EGOT	100126791							
chr3	4979411	4985180	3p26	3p26.1		604256	"BHLHE40, HLHB2, STRA13, DEC1"	"Basic helix-loop-helix family, member E40"	BHLHE40	8553	ENSG00000134107			Bhlhe40 (MGI:1097714)			
chr3	5122244	5180915	3p26.1	3p26.1		616596	"ARL8B, GIE1"	ADP-ribosylation factor-like 8B	ARL8B	55207	ENSG00000134108			Arl8b (MGI:1914416)			
chr3	5187673	5219964	3p26.1	3p26.1		607673	"EDEM, KIAA0212"	ER degradation-enhancing alpha-mannosidase-like protein	EDEM1	9695	ENSG00000134109			Edem1 (MGI:2180139)			
chr3	6861114	7743037	3p26.1	3p26.1		604101	"GRM7, MGLUR7"	"Glutamate receptor, metabotropic, 7"	GRM7	2917	ENSG00000196277			Grm7 (MGI:1351344)			
chr3	8100000	43600000	3p25-p22			607893	OVCAS1	"Ovarian cancer, susceptibility to, 1"		574048		between D3S1597 and D3S3611	"{Ovarian cancer, susceptibility to}, 607893 (2)"				
chr3	8100000	16300000	3p25			602011	"ST11, PETS1"	"Suppression of tumorigenicity 11, pancreas"	ST11	8466			?Pancreatic endocrine tumors (1)				
chr3	8501806	8568124	3p26-p24	3p25.3		604859	LMCD1	LIM and cysteine-rich domains 1	LMCD1	29995	ENSG00000071282			Lmcd1 (MGI:1353635)			
chr3	8619399	8745034	3p26.1-p25.3	3p25.3		617479	"SSUH2, C3orf32, FLS485"	"Ssu2, C. elegans, homolog of"	SSUH2	51066	ENSG00000125046			Ssu2 (MGI:2443733)			
chr3	8733799	8746764	3p25	3p25.3		601253	"CAV3, LGMD1C, LQT9"	Caveolin-3	CAV3	859	ENSG00000182533	within 7-10kb of OXTR	"Cardiomyopathy, familial hypertrophic, 192600 (3), Autosomal dominant; Creatine phosphokinase, elevated serum, 123320 (3), Autosomal dominant; Long QT syndrome 9, 611818 (3), Autosomal dominant; Muscular dystrophy, limb-girdle, type IC, 607801 (3), Autosomal recessive, Autosomal dominant; Myopathy, distal, Tateyama type, 614321 (3), Autosomal dominant; Rippling muscle disease, 606072 (3), Autosomal dominant"	Cav3 (MGI:107570)			
chr3	8750407	8769613	3p26.2	3p25.3		167055	OXTR	Oxytocin receptor	OXTR	5021	ENSG00000180914	3p25 by others; within 7-10kb of CAV3		Oxtr (MGI:109147)			
chr3	8877195	8969248	3p25-p24	3p25.3		605256	RAD18	"Rad18, S. cerevisiae, homolog of"	RAD18	56852	ENSG00000070950			Rad18 (MGI:1890476)			
chr3	8980590	9363445	3p25	3p25.3		606525	"SRGAP3, KIAA0411, MEGAP"	"Slit-robo GTPase-activating protein, rho, 3"	SRGAP3	9901	ENSG00000196220			Srgap3 (MGI:2152938)			
chr3	9397699	9478153	3p25.3	3p25.3		615743	"SETD5, KIAA1757"	SET domain-containing protein 5	SETD5	55209	ENSG00000168137		"Mental retardation, autosomal dominant 23, 615761 (3), Autosomal dominant"	Setd5 (MGI:1920145)			
chr3	9498360	9553801	3p25	3p25.3		610240	LHFPL4	LHFP-like protein 4	LHFPL4	375323	ENSG00000156959			Lhfpl4 (MGI:3057108)			
chr3	9649432	9702393	3p25.3	3p25.3		611089	"MTMR14, C3orf29, HJUMPY"	Myotubularin-related protein 14	MTMR14	64419	ENSG00000163719		"{Centronuclear myopathy, autosomal, modifier of}, 160150 (3), Autosomal dominant"	Mtmr14 (MGI:1916075)			
chr3	9731728	9748014	3p26-p25	3p25.3		602410	"BRPF1, BR140, IDDDFP"	"Bromodomain- and PHD finger-containing protein 1, 140kD"	BRPF1	7862	ENSG00000156983		"Intellectual developmental disorder with dysmorphic facies and ptosis, 617333 (3), Autosomal dominant"	Brpf1 (MGI:1926033)			
chr3	9749943	9788245	3p26.2	3p25.3		601982	OGG1	8-hydroxyguanine DNA glycosylase	OGG1	4968	ENSG00000114026		"Renal cell carcinoma, clear cell, somatic, 144700 (3)"	Ogg1 (MGI:1097693)			
chr3	9757344	9769986	3p25.3	3p25.3		604998	"CAMK1, CAMKI"	Calcium/calmodulin-dependent protein kinase I	CAMK1	8536	ENSG00000134072			Camk1 (MGI:1098535)			
chr3	9779963	9793010	3p25.3	3p25.3		602945	"TADA3, TADA3L, ADA3"	Transcriptional adaptor 3	TADA3	10474	ENSG00000171148			Tada3 (MGI:1915724)			
chr3	9792494	9807104	3p25.3	3p25.3		604226	"ARPC4, ARC20"	"Actin-related protein 2/3 complex, subunit 4"	ARPC4	10093	ENSG00000241553			Arpc4 (MGI:1915339)			
chr3	9836252	9844058	3p25.3	3p25.3		617759	RPUSD3	RNA pseudouridylate synthase domain-containing protein 3	RPUSD3	285367	ENSG00000156990			Rpusd3 (MGI:2141440)			
chr3	9866709	9880253	3p25	3p25.3		612120	"CIDEC, FSP27, CIDE3, FPLD5"	Cell death-inducing DFFA-like effector C	CIDEC	63924	ENSG00000187288	1 patient identified with mutation	"?Lipodystrophy, familial partial, type 5, 615238 (3), Autosomal recessive"	Cidec (MGI:95585)			
chr3	9890586	9894348	3p25.3	3p25.3		616012	"JAGN1, SCN6"	"Jagunal, Drosophila, homolog of, 1"	JAGN1	84522	ENSG00000171135		"Neutropenia, severe congenital, 6, autosomal recessive, 616022 (3), Autosomal recessive"	Jagn1 (MGI:1915017)			
chr3	9902086	9916401	3p25.3	3p25.3		614995	IL17RE	Interleukin 17 receptor E	IL17RE	132014	ENSG00000163701			Il17re (MGI:1889371)			
chr3	9917073	9933626	3p25.3-p24.1	3p25.3		610925	"IL17RC, IL17RL, CANDF9"	Interleukin 17 receptor C	IL17RC	84818	ENSG00000163702		"Candidiasis, familial, 9, 616445 (3), Autosomal recessive"	Il17rc (MGI:2159336)			
chr3	9933787	9945412	3p25.3	3p25.3		607170	"CRELD1, AVSD2"	Cysteine-rich protein with EGF-like domains 1	CRELD1	78987	ENSG00000163703		"Atrioventricular septal defect, partial, with heterotaxy syndrome, 606217 (3), Autosomal dominant; {Atrioventricular septal defect, susceptibility to, 2}, 606217 (3), Autosomal dominant"	Creld1 (MGI:2152539)			
chr3	10026386	10101936	3p25.3	3p25.3		613984	"FANCD2, FANCD, FACD, FAD"	"Fanconi anemia, complementation group D2"	FANCD2	2177	ENSG00000144554		"Fanconi anemia, complementation group D2, 227646 (3), Autosomal recessive"	Fancd2 (MGI:2448480)			
chr3	10115648	10127189	3p25.3	3p25.3		611183	"BRK1, C3orf10, HSPC300"	"BRICK1, SCAR/WAVE actin-nucleating complex subunit"	BRK1	55845	ENSG00000254999			Brk1 (MGI:1915406)			
chr3	10141634	10153669	3p26-p25	3p25.3		608537	VHL	VHL gene	VHL	7428	ENSG00000134086		"Erythrocytosis, familial, 2, 263400 (3), Autosomal recessive; Hemangioblastoma, cerebellar, somatic (3); Pheochromocytoma, 171300 (3), Autosomal dominant; Renal cell carcinoma, somatic, 144700 (3); von Hippel-Lindau syndrome, 193300 (3), Autosomal dominant"	Vhl (MGI:103223)			
chr3	10164878	10243742	3p25.3	3p25.3		603304	IRAK2	Interleukin 1 receptor-associated kinase 2	IRAK2	3656	ENSG00000134070			Irak2 (MGI:2429603)			
chr3	10285749	10292946	3p26-p25	3p25.3		605353	GHRL	Ghrelin	GHRL	51738	ENSG00000157017		"{Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Ghrl (MGI:1930008)			
chr3	10300928	10321187	3p25-p24	3p25.3		600152	"SEC13L1, D3S1231E, SEC13R"	"SEC13, S. cerevisiae, like 1"	SEC13	6396	ENSG00000157020			Sec13 (MGI:99832)			
chr3	10324022	10707961	3p26-p25	3p25.3		108733	"ATP2B2, PMCA2"	"ATPase, Ca++ transporting, plasma membrane, 2"	ATP2B2	491	ENSG00000157087		"{Deafness, autosomal recessive 12, modifier of}, 601386 (3), Autosomal recessive"	Atp2b2 (MGI:105368)			
chr3	10816199	10940732	3p25.3	3p25.3		607952	"SLC6A11, GAT3, GAT4"	"Solute carrier family 6 (neurotransmitter transporter, GABA), member 11"	SLC6A11	6538	ENSG00000132164			Slc6a11 (MGI:95630)			
chr3	10992733	11039248	3p25-p24	3p25.3		137165	"SLC6A1, GABATR, MAE"	"Solute carrier family 6 (neurotransmitter transporter, GABA), member 1"	SLC6A1	6529	ENSG00000157103		"Myoclonic-atonic epilepsy, 616421 (3), Autosomal dominant"	Slc6a1 (MGI:95627)			
chr3	11137092	11263252	3p21-p14	3p25.3		600167	HRH1	"Histamine receptor, subclass H1"	HRH1	3269	ENSG00000196639			Hrh1 (MGI:107619)			
chr3	11272323	11564651	3p25.3	3p25.3		608760	"ATG7, APG7L, GSA7"	"Autophagy 7, S. cerevisiae, homolog of"	ATG7	10533	ENSG00000197548			Atg7 (MGI:1921494)			
chr3	11600000	16300000	3p25.2-p25.1			606661	UVM2	"Melanoma, uveal, susceptibility to, 2"		170593			"{Melanoma, uveal, susceptibility to, 2}, 606661 (2)"				
chr3	11721895	11846918	3p25.2	3p25.2		614948	"TAMM41, RAM41, C3orf31"	"Translocator assembly and maintenance, mitochondrial, S. cerevisiae, homolog of"	TAMM41	132001	ENSG00000144559			Tamm41 (MGI:1916221)			
chr3	12004359	12192031	3p25	3p25.2		600755	SYN2	Synapsin II	SYN2	6854	ENSG00000157152		"{Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"	Syn2 (MGI:103020)			
chr3	12153067	12159350	3p25	3p25.2		601915	TIMP4	Tissue inhibitor of metalloproteinase 4	TIMP4	7079	ENSG00000157150			Timp4 (MGI:109125)			
chr3	12287484	12471053	3p25	3p25.2		601487	"PPARG, PPARG1, PPARG2, CIMT1, GLM1"	"Peroxisome proliferator activated receptor, gamma"	PPARG	5468	ENSG00000132170	"PPARG1, PPARG2 from same gene"	"Carotid intimal medial thickness 1, 609338 (3); {Diabetes, type 2}, 125853 (3), Autosomal dominant; Insulin resistance, severe, digenic, 604367 (3), Autosomal dominant; Lipodystrophy, familial partial, type 3, 604367 (3), Autosomal dominant; [Obesity, resistance to] (3); Obesity, severe, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Pparg (MGI:97747)			
chr3	12484431	12539623	3p25.1	3p25.2		608753	"TSEN2, SEN2, PCH2B"	"tRNA splicing endonuclease 2, S. cerevisiae, homolog of"	TSEN2	80746	ENSG00000154743		"Pontocerebellar hypoplasia type 2B, 612389 (3), Autosomal recessive"	Tsen2 (MGI:2141599)			
chr3	12557013	12583712	3p25	3p25.2		608426	MKRN2	Makorin 2	MKRN2	23609	ENSG00000075975			Mkrn2 (MGI:1914277)			
chr3	12583600	12664200	3p25	3p25.2		164760	"RAF1, CRAF, NS5, CMD1NN"	Oncogene RAF1	RAF1	5894	ENSG00000132155		"Cardiomyopathy, dilated, 1NN, 615916 (3), Autosomal dominant; LEOPARD syndrome 2, 611554 (3); Noonan syndrome 5, 611553 (3), Autosomal dominant"	Raf1 (MGI:97847)			
chr3	12796653	12834817	3p25.2	3p25.2		610403	"CAND2, TIP120B, KIAA0667"	Cullin-associated neddylation -dissociated 2	CAND2	23066	ENSG00000144712			Cand2 (MGI:1914338)			
chr3	12897042	13073409	3p25.2	3p25.2		610166	"IQSEC1, KIAA0763"	IQ motif- and Sec7 domain-containing protein 1	IQSEC1	9922	ENSG00000144711			Iqsec1 (MGI:1196356)			
chr3	13200000	32000000	3p25.1-p23			613530	LGMD1H	"Muscular dystrophy, limb-girdle, type 1H"	LGMD1H	100529230		between D3S1263 and D3S1277	"Muscular dystrophy, limb-girdle, type 1H, 613530 (2), Autosomal dominant"				
chr3	13316229	13420318	3p25.1	3p25.1		607703	"NUP210, GP210, KIAA0906"	"Nucleoporin, 210kD"	NUP210	23225	ENSG00000132182			Nup210 (MGI:1859555)			
chr3	13549124	13638421	3p25-p24	3p25.1		135821	FBLN2	Fibulin-2	FBLN2	2199	ENSG00000163520			Fbln2 (MGI:95488)			
chr3	13818107	13880120	3p25	3p25.1		601570	WNT7A	"Wingless-type MMTV integration site family, member 7A"	WNT7A	7476	ENSG00000154764		"Fuhrmann syndrome, 228930 (3), Autosomal recessive; Ulna and fibula, absence of, with severe limb deficiency, 276820 (3), Autosomal recessive"	Wnt7a (MGI:98961)			
chr3	13937306	14065983	3p25.1	3p25.1		611167	TPRXL	Tetrapeptide repeat homeobox-like	TPRXL	348825							
chr3	14112076	14124870	3p25.1	3p25.1		611077	"CHDH4, MIA40"	Coiled-coil-helix-coiled-coil-helix domain-containing protein 4	CHCHD4	131474	ENSG00000163528			Chchd4 (MGI:1919420)			
chr3	14124939	14143679	3p25	3p25.1		612048	"TMEM43, ARVD5, ARVC5, EDMD7"	Transmembrane protein 43	TMEM43	79188	ENSG00000170876		"Arrhythmogenic right ventricular dysplasia 5, 604400 (3), Autosomal dominant; Emery-Dreifuss muscular dystrophy 7, AD, 614302 (3), Autosomal dominant"	Tmem43 (MGI:1921372)			
chr3	14145144	14178671	3p25	3p25.1		613208	"XPC, XPCC"	XPC gene	XPC	7508	ENSG00000154767		"Xeroderma pigmentosum, group C, 278720 (3), Autosomal recessive"	Xpc (MGI:103557)			
chr3	14178727	14198368	3p25.1	3p25.1		607283	LSM3	LSM3 protein	LSM3	27258	ENSG00000170860			Lsm3 (MGI:1914928)			
chr3	14402575	14489348	3p25-q24	3p25.1		186854	"SLC6A6, TAUT"	"Solute carrier family 6 (neurotransmitter transporter, taurine), member 6"	SLC6A6	6533	ENSG00000131389			Slc6a6 (MGI:98488)			
chr3	14651745	14672658	3p25.1	3p25.1		616735	"CCDC174, HSPC212, IHPM"	Coiled-coil domain-containing protein 174	CCDC174	51244	ENSG00000154781		"Hypotonia, infantile, with psychomotor retardation, 616816 (3), Autosomal recessive"	Ccdc174 (MGI:2444652)			
chr3	14818961	14934564	3p25.1	3p25.1		614788	FGD5	"FYVE, RhoGEF, and PH domain-containing protein 5"	FGD5	152273	ENSG00000154783			Fgd5 (MGI:2443369)			
chr3	14947583	15049278	3p25	3p25.1		601426	"NR2C2, TR4, TAK1"	"Nuclear receptor subfamily 2, group C, member 2"	NR2C2	7182	ENSG00000177463			Nr2c2 (MGI:1352466)			
chr3	15042250	15065336	3p25	3p25.1		611987	MRPS25	Mitochondrial ribosomal protein S25	MRPS25	64432	ENSG00000131368			Mrps25 (MGI:1928140)			
chr3	15070068	15099162	3p25.1	3p25.1		609511	"RBSN,  ZFYVE20"	Rabenosyn 5	RBSN	64145	ENSG00000131381			Rbsn (MGI:1925537)			
chr3	15165361	15205958	3p24.3	3p25.1		612397	"COL6A4P1, DVWA, DIVA, LOC344875"	"Collagen, type VI, alpha 4, pseudogene 1"	COL6A4P1	344875							
chr3	15206225	15252915	3p24	3p25.1		606400	"CAPN7, PALBH"	Calpain 7	CAPN7	23473	ENSG00000131375			Capn7 (MGI:1338030)			
chr3	15254352	15341393	3p25.1	3p25.1		605612	"SH3BP5, SAB"	SH3 domain-binding protein 5	SH3BP5	9467	ENSG00000131370	previously mapped to 1q431		Sh3bp5 (MGI:1344391)			
chr3	15427556	15442612	3p25.1	3p25.1		608315	EAF1	ELL-associated factor 1	EAF1	85403	ENSG00000144597			Eaf1 (MGI:1921677)			
chr3	15450132	15521750	3p25	3p25.1		603033	"COLQ, EAD, CMS5"	Collagenic tail of endplate acetylcholinesterase	COLQ	8292	ENSG00000206561		"Myasthenic syndrome, congenital, 5, 603034 (3), Autosomal recessive"				
chr3	15560703	15601851	3p25.1	3p25.1		604300	"HACL1, HPCL2"	2-hydroxyacyl-CoA lyase 1	HACL1	26061	ENSG00000131373			Hacl1 (MGI:1929657)			
chr3	15601351	15653710	3p25	3p25.1		609019	BTD	Biotinidase	BTD	686	ENSG00000169814		"Biotinidase deficiency, 253260 (3), Autosomal recessive"	Btd (MGI:1347001)			
chr3	15667235	15859812	3p25.1	3p25.1		611122	"ANKRD28, PITK, KIAA0379"	Ankyrin repeat domain-containing protein 28	ANKRD28	23243	ENSG00000206560			Ankrd28 (MGI:2145661)			
chr3	16174321	16248223	3p25.1	3p25.1		615131	"GALNT15, GALNACT15"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 15	GALNT15	117248	ENSG00000131386			Galnt15 (MGI:1926004)			
chr3	16257060	16264988	3p24.3	3p25.1		608959	"DPH3, KTI11, ZCSL2, DELGIP1"	"DPH3, S. cerevisiae, homolog of"	DPH3	285381	ENSG00000154813			Dph3 (MGI:1922658)			
chr3	16300000	54400000	3p24-p21			609954	ASPG4	"Asperger syndrome, susceptibility to, 4"		100188800		max lod at D3S2432	"{Asperger syndrome susceptibility 4}, 609954 (2)"				
chr3	16300000	30800000	3p24			613519	ATOD9	"Dermatitis, atopic, 9"		105463126		max lod at D3S1768	"{Dermatitis, atopic, susceptibility to, 9}, 613519 (2)"				
chr3	16300000	43600000	3p24-p22			608088	HSN1B	"Hereditary sensory neuropathy, type IB"		378888		max lod at D3S2338	"Neuropathy, hereditary sensory, type IB, 608088 (2), Autosomal dominant"				
chr3	16300000	23800000	3p24.3			612401	OS6	Osteoarthritis susceptibility 6		100286836		associated with rs11718863 and rs7639618	"{Osteoarthritis susceptibility 6}, 612401 (2)"				
chr3	16300000	52300000	3p24-p21.2			609649	TRICY1	Trichilemmal cyst 1	TRICY1	94014		max lod at D3S1277	"Trichilemmal cyst 1, 609649 (2), Autosomal dominant"				
chr3	16586791	16605498	3p24	3p24.3		601486	"DAZL, DAZH, SPGYLA"	Deleted in azoospermia-like	DAZL	1618	ENSG00000092345	?founding member of DAZ gene family	"{Spermatogenic failure, susceptibility to} (3)"				
chr3	16802690	17090605	3p25-p24	3p24.3		614276	"PLCL2, KIAA1092"	Phospholipase C-like 2	PLCL2	23228	ENSG00000154822			Plcl2 (MGI:1352756)			
chr3	17157161	17742738	3p24.3	3p24.3		615740	"TBC1D5, KIAA0210"	"TBC1 domain family, member 5"	TBC1D5	9779	ENSG00000131374			Tbc1d5 (MGI:1919488)			
chr3	18345387	18445587	3p23	3p24.3		602075	SATB1	Special AT-rich sequence binding protein-1	SATB1	6304	ENSG00000182568			Satb1 (MGI:105084)			
chr3	19947079	19985174	3p24-p22	3p24.3		179512	"RAB5A, RAB5"	RAS-associated protein RAB5A	RAB5A	5868	ENSG00000144566			Rab5a (MGI:105926)			
chr3	20040031	20154403	3p24	3p24.3		602303	CAF	CREBBP-associated factor	KAT2B	8850	ENSG00000114166			Kat2b (MGI:1343094)			
chr3	20160592	20188142	3p24.3	3p24.3		609168	"SGOL1, SGO, SGO1, CAID"	Shugoshin-like 1	SGO1	151648	ENSG00000129810		"Chronic atrial and intestinal dysrhythmia, 616201 (3), Autosomal recessive"	Sgo1 (MGI:1919665)			
chr3	23203006	23590804	3p24.2	3p24.3		602163	UBE2E2	Ubiquitin-conjugating enzyme E2E 2 (homologous to yeast UBC4/5)	UBE2E2	7325	ENSG00000182247			Ube2e2 (MGI:2384997)			
chr3	23800000	32000000	3p24.2-p23			611634	9-Feb	"Febrile seizures, familial, 9"		100188849		between D3S3727 and D3S3567	"Febrile seizures, familial, 9, 611634 (2), Autosomal dominant"				
chr3	23805892	23891639	3p24.3-p24.2	3p24.2		602916	"UBE2E1, UBCH6"	Ubiquitin-conjugating enzyme E2E 1	UBE2E1	7324	ENSG00000170142			Ube2e1 (MGI:107411)			
chr3	23916544	23924630	3p24.2	3p24.2		604174	"RPL15, DBA12"	Ribosomal protein L15	RPL15	6138	ENSG00000174748	mutation identified in 1 family	"?Diamond-Blackfan anemia 12, 615550 (3), Autosomal dominant"	Rpl15 (MGI:1913730)			
chr3	23945259	23980617	3p24.3	3p24.2		602304	"NR1D2, RVR, BD73"	"Nuclear receptor subfamily 1, group D, member 2"	NR1D2	9975	ENSG00000174738			Nr1d2 (MGI:2449205)			
chr3	24117152	24495280	3p24.3	3p24.2		190160	"THRB, ERBA2, THR1, PRTH"	"Thyroid hormone receptor, beta (avian erythroblastic leukemia viral (v-erb-a) oncogene homolog-2)"	THRB	7068	ENSG00000151090		"Thyroid hormone resistance, 188570 (3), Autosomal dominant; Thyroid hormone resistance, autosomal recessive, 274300 (3), Autosomal recessive; Thyroid hormone resistance, selective pituitary, 145650 (3), Autosomal dominant"	Thrb (MGI:98743)			
chr3	24829322	25597931	3p24	3p24.2		180220	"RARB, HAP, MCOPS12"	"Retinoic acid receptor, beta polypeptide"	RARB	5915	ENSG00000077092	#NAME?	"Microphthalmia, syndromic 12, 615524 (3), Autosomal recessive, Autosomal dominant"	Rarb (MGI:97857)			
chr3	25597904	25664890	3p24	3p24.2		126431	TOP2B	"Topoisomerase (DNA) II, beta, 180kD"	TOP2B	7155	ENSG00000077097			Top2b (MGI:98791)			
chr3	25718943	25790038	3p24	3p24.2		610661	"NGLY1, PNG1, CDDG, CDG1V"	N-glycanase 1	NGLY1	55768	ENSG00000151092		"Congenital disorder of deglycosylation, 615273 (3), Autosomal recessive"	Ngly1 (MGI:1913276)			
chr3	25788282	25794533	3p24.2	3p24.2		610324	"OXSM, KS"	"3-oxoacyl-ACP synthase, mitochondrial"	OXSM	54995	ENSG00000151093			Oxsm (MGI:1918397)			
chr3	27372720	27484419	3p22	3p24.1		603353	"SLC4A7, NBC2, NBC3"	"Solute carrier family 4, sodium bicarbonate cotransporter, member 7"	SLC4A7	9497	ENSG00000033867			Slc4a7 (MGI:2443878)			
chr3	27715948	27722714	3p21.3-p21.2	3p24.1		604615	"EOMES, TBR2"	"Eomesodermin, Xenopus laevis, homolog of"	EOMES	8320	ENSG00000163508	?translocation separating regulatory element from promoter		Eomes (MGI:1201683)			
chr3	28241592	28319775	3p24	3p24.1		615166	"CMC1, C3orf68"	"Cytochrome C oxidase assembly mitochondrial protein 1, S. cerevisiae, homolog of"	CMC1	152100	ENSG00000187118			Cmc1 (MGI:1915149)			
chr3	28322352	28349277	3p24.1	3p24.1		609916	"AZI2, AZ2, NAP1, TILP"	"5-azacytidine-induced gene 2, mouse, homolog of"	AZI2	64343	ENSG00000163512			Azi2 (MGI:1351332)			
chr3	29280859	30010394	3p24-p23	3p24.1		605786	RBMS3	"RNA-binding motif protein, single strand-interacting, 3"	RBMS3	27303	ENSG00000144642			Rbms3 (MGI:2444477)			
chr3	30606471	30694141	3p24.1	3p24.1		190182	"TGFBR2, HNPCC6, AAT3, MFS2, LDS2"	"Transforming growth factor, beta receptor II, 70-80kD"	TGFBR2	7048	ENSG00000163513		"Colorectal cancer, hereditary nonpolyposis, type 6, 614331 (3); Esophageal cancer, somatic, 133239 (3); Loeys-Dietz syndrome 2, 610168 (3), Autosomal dominant"	Tgfbr2 (MGI:98729)			
chr3	30726008	30894660	3p24.1	3p24-p23		615601	GADL1	Glutamate decarboxylase-like 1	GADL1	339896	ENSG00000144644			Gadl1 (MGI:1920998)			
chr3	30800000	54400000	3p23-p21			182280	SCLC1	Small-cell cancer of lung		7864		centromeric to ERBA2	"Small-cell cancer of lung, 182280 (2), Autosomal dominant"				
chr3	31532500	31637621	3p23	3p23		608605	"STT3B, SIMP, CDG1X"	"STT3B, subunit of the oligosaccharyltransferase complex (catalytic)"	STT3B	201595	ENSG00000163527	mutation identified in 1 family	"?Congenital disorder of glycosylation, type Ix, 615597 (3), Autosomal recessive"	Stt3b (MGI:1915542)			
chr3	31660824	31981849	3p25.3-p22	3p23		606738	"OSBPL10, ORP10"	Oxysterol-binding protein-like protein 10	OSBPL10	114884	ENSG00000144645			Osbpl10 (MGI:1921736)			
chr3	32000000	43600000	3p22			614836	HHV8S	"Human herpesvirus 8, susceptibility to"		101056702			"{Human herpesvirus 8, susceptibility to}, 614836 (2)"				
chr3	32106510	32168714	3p22.3	3p22.3		611778	"GPD1L, KIAA0089"	Glycerol-3-phosphate dehydrogenase 1-like	GPD1L	23171	ENSG00000152642		"Brugada syndrome 2, 611777 (3)"	Gpd1l (MGI:1289257)			
chr3	32238678	32370324	3p22.3	3p22.3		607891	"CMTM8, CKLFSF8"	CKLF-like marvel transmembrane domain-containing 8	CMTM8	152189	ENSG00000170293			Cmtm8 (MGI:2447167)			
chr3	32391670	32455527	3p22.3	3p22.3		607890	"CMTM7, CKLFSF7"	CKLF-like marvel transmembrane domain-containing 7	CMTM7	112616	ENSG00000153551			Cmtm7 (MGI:2447166)			
chr3	32481311	32502910	3p22.3	3p22.3		607889	"CMTM6, CKLFSF6"	CKLF-like marvel transmembrane domain-containing 6	CMTM6	54918	ENSG00000091317			Cmtm6 (MGI:2447165)			
chr3	32525970	32570923	3p22.3	3p22.3		615890	"DYNC1LI1, LIC1"	"Dynein, cytoplasmic 1, light intermediate chain 1"	DYNC1LI1	51143	ENSG00000144635			Dync1li1 (MGI:2135610)			
chr3	32951554	32955311	3p24	3p22.3		604836	"CCR4, CKR4, CMKBR4"	Chemokine (C-C) receptor-4	CCR4	1233	ENSG00000183813			Ccr4 (MGI:107824)			
chr3	32996607	33097229	3p21.33	3p22.3		611458	"GLB1, MPS4B"	"Galactosidase, beta-1"	GLB1	2720	ENSG00000170266	3p14.2-p11 excluded	"GM1-gangliosidosis, type I, 230500 (3), Autosomal recessive; GM1-gangliosidosis, type II, 230600 (3), Autosomal recessive; GM1-gangliosidosis, type III, 230650 (3), Autosomal recessive; Mucopolysaccharidosis type IVB (Morquio), 253010 (3), Autosomal recessive"	Glb1 (MGI:88151)			
chr3	33113957	33147772	3p22	3p22.3		605497	"CRTAP, CASP, OI7"	Cartilage-associated protein	CRTAP	10491	ENSG00000170275		"Osteogenesis imperfecta, type VII, 610682 (3), Autosomal recessive"	Crtap (MGI:1891221)			
chr3	33277024	33422697	3p22.3	3p22.3		605652	"FBXL2, FBL2"	F-box and leucine-rich repeat protein 2	FBXL2	25827	ENSG00000153558			Fbxl2 (MGI:1919429)			
chr3	33388335	33440404	3p23	3p22.3		609784	"UBP1, LBP1A, LBP1B"	Upstream binding protein 1	UBP1	7342	ENSG00000153560			Ubp1 (MGI:104889)			
chr3	33496244	33718355	3p22.3	3p22.3		605853	CLASP2	CLIP-associated protein 2	CLASP2	23122	ENSG00000163539			Clasp2 (MGI:1923749)			
chr3	33798570	33869706	3p22.3	3p22.3		608074	"PDCD6IP, AIP1, ALIX, KIAA1375"	Programmed cell death 6-interacting protein	PDCD6IP	10015	ENSG00000170248			Pdcd6ip (MGI:1333753)			
chr3	35744475	35744558	3p22	3p22.3		611769	"MIR128-2, MIR128B, MIRN128-2"	Micro RNA 128-2	MIR128-2	406916							
chr3	36380342	36548006	3p24-p22	3p22.3-p22.2		602317	STAC	SRC homology three (SH3) and cysteine-rich domain	STAC	6769	ENSG00000144681			Stac (MGI:1201400)			
chr3	36400000	39300000	3p22.2			615612	DDH2	Developmental dysplasia of the hip 2		102775567		between rs4481097 and rs4626072	"Developmental dysplasia of the hip 2, 615612 (2), Autosomal dominant"				
chr3	36712421	36764205	3p22.3	3p22.2		613167	"DCLK3, DCK3, CLR"	Doublecortin-like kinase 3	DCLK3	85443	ENSG00000163673			Dclk3 (MGI:3039580)			
chr3	36985865	36993303	3p22.1	3p22.2		607911	"EPM2AIP1, KIAA0766"	EPM2A-interacting protein 1	EPM2AIP1	9852	ENSG00000178567			Epm2aip1 (MGI:1925031)			
chr3	36993349	37050845	3p21.3	3p22.2		120436	"MLH1, COCA2, HNPCC2"	"mutL, E. coli, homolog of, 1"	MLH1	4292	ENSG00000076242		"Colorectal cancer, hereditary nonpolyposis, type 2, 609310 (3); Mismatch repair cancer syndrome, 276300 (3), Autosomal recessive; Muir-Torre syndrome, 158320 (3), Autosomal dominant"	Mlh1 (MGI:101938)			
chr3	37052625	37176816	3p22.2	3p22.2		614043	LRRFIP2	Leucine-rich repeat in FLII-interacting protein 2	LRRFIP2	9209	ENSG00000093167						
chr3	37243190	37366878	3p22-p21.3	3p22.2		602509	GOLGA4	"Golgi autoantigen, golgin subfamily a, 4"	GOLGA4	2803	ENSG00000144674			Golga4 (MGI:1859646)			
chr3	37452321	37819789	3p21.3	3p22.2		603963	ITGA9	"Integrin, alpha-9"	ITGA9	3680	ENSG00000144668			Itga9 (MGI:104756)			
chr3	37969403	37969479	3p22.2	3p22.2		612151	"MIR26A, MIRN26A1"	Micro RNA 26A1	MIR26A1	407015							
chr3	38007495	38029662	3p22-p21.3	3p22.2		602142	"PLCD1, NDNC3"	"Phospholipase C, delta-1"	PLCD1	5333	ENSG00000187091		"Nail disorder, nonsyndromic congenital, 3, (leukonychia), 151600 (3), Autosomal recessive, Autosomal dominant"	Plcd1 (MGI:97614)			
chr3	38038594	38122740	3p22-p21.3	3p22.2		604050	"DLEC1, DLC1"	Deleted in lung and esophageal cancer 1	DLEC1	9940	ENSG00000008226		"Esophageal cancer, 133239 (1), Autosomal dominant; Lung cancer, 211980 (1), Autosomal recessive"	Dlec1 (MGI:2443671)			
chr3	38122709	38137241	3p23-p22	3p22.2		604054	ACAA1	Acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3-oxoacyl-Coenzyme A thiolase)	ACAA1	30	ENSG00000060971			Acaa1a (MGI:2148491)			
chr3	38137438	38143021	3p22-p21.3	3p22.2		602170	"MYD88, MYD88D"	Myeloid differentiation primary response gene 88	MYD88	4615	ENSG00000172936		"Macroglobulinemia, Waldenstrom, somatic, 153600 (3); Pyogenic bacterial infections, recurrent, due to MYD88 deficiency, 612260 (3)"	Myd88 (MGI:108005)			
chr3	38165050	38255487	3p22-p21.3	3p22.2		604046	OSR1	Oxidative stress-responsive 1	OXSR1	9943	ENSG00000172939			Oxsr1 (MGI:1917378)			
chr3	38346759	38453040	3p22-p21.3	3p22.2		604049	XYLB	"Xylulokinase, H. influenzae, homolog of"	XYLB	9942	ENSG00000093217			Xylb (MGI:2142985)			
chr3	38454298	38493141	3p22-p21.3	3p22.2		602730	"ACVR2B, ACTRIIB, HTX4"	"Activin A receptor, type IIB"	ACVR2B	93	ENSG00000114739		"Heterotaxy, visceral, 4, autosomal, 613751 (3)"	Acvr2b (MGI:87912)			
chr3	38496126	38526304	3p22-p21.3	3p22.2		604051	"EXOG, ENDOGL1, ENGL"	"Endo/exonuclease, ENDOG-like"	EXOG	9941	ENSG00000157036			Exog (MGI:2143333)			
chr3	38548060	38649672	3p21	3p22.2		600163	"SCN5A, LQT3, VF1, HB1, SSS1, CMD1E, CDCD2"	"Sodium channel, voltage-gated, type V, alpha polypeptide"	SCN5A	6331	ENSG00000183873		"Atrial fibrillation, familial, 10, 614022 (3), Autosomal dominant; Brugada syndrome 1, 601144 (3), Autosomal dominant; Cardiomyopathy, dilated, 1E, 601154 (3), Autosomal dominant; Heart block, nonprogressive, 113900 (3), Autosomal dominant; Heart block, progressive, type IA, 113900 (3), Autosomal dominant; Long QT syndrome-3, 603830 (3), Autosomal dominant; Sick sinus syndrome 1, 608567 (3), Autosomal recessive; {Sudden infant death syndrome, susceptibility to}, 272120 (3), Autosomal recessive; Ventricular fibrillation, familial, 1, 603829 (3)"	Scn5a (MGI:98251)			
chr3	38697109	38794009	3p22.2	3p22.2		604427	"SCN10A, FEPS2"	"Sodium channel, voltage-gated, type X, alpha subunit"	SCN10A	6336	ENSG00000185313		"Episodic pain syndrome, familial, 2, 615551 (3), Autosomal dominant"	Scn10a (MGI:108029)			
chr3	38845763	39051944	3p22.2	3p22.2		604385	"SCN11A, HSAN7, FEPS3"	"Sodium channel, voltage-gated, type XI, alpha subunit"	SCN11A	11280	ENSG00000168356		"Episodic pain syndrome, familial, 3, 615552 (3), Autosomal dominant; Neuropathy, hereditary sensory and autonomic, type VII, 615548 (3), Autosomal dominant"	Scn11a (MGI:1345149)			
chr3	39051985	39096670	3p21.33	3p22.2		612167	"WDR48, KIAA1449"	WD repeat-containing protein 48	WDR48	57599	ENSG00000114742			Wdr48 (MGI:1914811)			
chr3	39096598	39108362	3p21.3	3p22.2		606867	"GORASP1, GOLPH5, GRASP65, P65"	"Golgi reassembly stacking protein 1, 65kD"	GORASP1	64689	ENSG00000114745			Gorasp1 (MGI:1921748)			
chr3	39141850	39154601	3p22	3p22.2		606458	AXUD1	Axin1 upregulated	CSRNP1	64651	ENSG00000144655			Csrnp1 (MGI:2387989)			
chr3	39183209	39192620	3p22.2	3p22.2		609777	"CMYA1, XIN"	Cardiomyopathy-associated protein 1	XIRP1	165904	ENSG00000168334			Xirp1 (MGI:1333878)			
chr3	39263493	39281734	3pter-p21	3p22.2		601470	"CX3CR1, GPR13, V28"	Chemokine (C-X3-C) receptor 1 (G protein-coupled receptor-13)	CX3CR1	1524	ENSG00000168329		"{Coronary artery disease, resistance to}, 607339 (3); {Macular degeneration, age-related, 12}, 613784 (3); {Rapid progression to AIDS from HIV1 infection}, 609423 (3)"	Cx3cr1 (MGI:1333815)			
chr3	39329705	39333679	3p22	3p22.1		601834	"CCR8, CMKBR8, CMKBRL2, CKRL1"	Chemokine (C-C) receptor 8	CCR8	1237	ENSG00000179934			Ccr8 (MGI:1201402)			
chr3	39383323	39397350	3p22.1	3p22.1		610819	"SLC25A38, SIDBA2"	"Solute carrier family 25, member 38"	SLC25A38	54977	ENSG00000144659		"Anemia, sideroblastic, 2, pyridoxine-refractory, 205950 (3), Autosomal recessive"	Slc25a38 (MGI:2384782)			
chr3	39406688	39412541	3p21.3	3p22.1		150370	"RPSA, LAMR1, LAMBR, ICAS"	Ribosomal protein SA	RPSA	3921	ENSG00000168028		"Asplenia, isolated congenital, 271400 (3), Autosomal dominant"	Rpsa (MGI:105381)			
chr3	39411053	39411206	3p22.1	3p22.1		180646	"SNORA62, RNU108, RNE2"	"Small nucleolar RNA, H/ACA box, 62"	SNORA62	6044							
chr3	39467572	39529496	3p22-p21	3p22.1		600948	MOBP	Myelin-associated oligodendrocyte basic protein	MOBP	4336	ENSG00000168314			Mobp (MGI:108511)			
chr3	39808913	40260320	3p21.33-p21.32	3p22.1		611790	"MYRIP, SLAC2C"	Myosin VIIA- and RAB-interacting protein	MYRIP	25924	ENSG00000170011			Myrip (MGI:2384407)			
chr3	40387155	40428625	3p21.3	3p22.1		603161	"ENTPD3, CD39L3"	Ectonucleoside triphosphate diphosphohydrolase 3	ENTPD3	956	ENSG00000168032			Entpd3 (MGI:1321386)			
chr3	40457291	40462371	3p22.1	3p22.1		617414	RPL14	Ribosomal protein L14	RPL14	9045	ENSG00000188846			Rpl14 (MGI:1914365)			
chr3	41199421	41240452	3p22.1	3p22.1		116806	"CTNNB1, MRD19, EVR7"	"Catenin (cadherin-associated protein), beta 1, 88kD"	CTNNB1	1499	ENSG00000168036		"Colorectal cancer, somatic, 114500 (3); Exudative vitreoretinopathy 7, 617572 (3), Autosomal dominant; Hepatocellular carcinoma, somatic, 114550 (3); Medulloblastoma, somatic, 155255 (3); Mental retardation, autosomal dominant 19, 615075 (3), Autosomal dominant; Ovarian cancer, somatic, 167000 (3); Pilomatricoma, somatic, 132600 (3)"	Ctnnb1 (MGI:88276)			
chr3	41246598	41962439	3p22.1	3p22.1		617010	"ULK4, FAM7C1"	Unc51-like kinase 4	ULK4	54986	ENSG00000168038			Ulk4 (MGI:1921622)			
chr3	42013801	42225889	3p25.3-p24.1	3p22.1		608112	"TRAK1, OIP106, KIAA1042"	"Trafficking protein, kinesin-binding 1"	TRAK1	22906	ENSG00000182606			Trak1 (MGI:1914345)			
chr3	42257823	42266194	3pter-p21	3p22.1		118440	CCK	Cholecystokinin	CCK	885	ENSG00000187094			Cck (MGI:88297)			
chr3	42360765	42411793	3p21.33	3p22.1		612750	LYZL4	Lysozyme-like 4	LYZL4	131375	ENSG00000157093			Lyzl4 (MGI:1916282)			
chr3	42489298	42537572	3p22	3p22.1		192321	VIPR1	Vasoactive intestinal peptide receptor 1	VIPR1	7433	ENSG00000114812	incorrectly assigned to 2q37		Vipr1 (MGI:109272)			
chr3	42547966	42603126	3p22.1	3p22.1		604028	SEC22C	"Secretion deficient 22, S. cerevisiae, homolog of, C"	SEC22C	9117	ENSG00000093183			Sec22c (MGI:2447871)			
chr3	42581839	42594997	3p21	3p22.1		606473	SS18L2	SS18-like gene 2	SS18L2	51188	ENSG00000008324			Ss18l2 (MGI:1349474)			
chr3	42600006	42648740	3p22.1	3p22.1		161565	NKTR	Natural tumor-killer recognition sequence	NKTR	4820	ENSG00000114857	mouse gene close to Cck		Nktr (MGI:97346)			
chr3	42685518	42692445	3p22.1	3p22.1		615340	"KLHL40, SYRP, KBTBD5, NEM8"	Kelch-like 40	KLHL40	131377	ENSG00000157119		"Nemaline myopathy 8, autosomal recessive, 615348 (3)"	Klhl40 (MGI:1919580)			
chr3	42692662	42702848	3p22.1	3p22.1		608116	"HHATL, MBOAT3, C3orf3, KIAA1173"	Hedgehog acyltransferase-like protein	HHATL	57467	ENSG00000010282			Hhatl (MGI:1922020)			
chr3	42809471	42867282	3p21.3	3p22.1		602648	"ACKR2, CCBP2, CMKBR9, D6, CCR9, CCR10"	Atypical chemokine receptor 2	ACKR2	1238	ENSG00000144648			Ackr2 (MGI:1891697)			
chr3	42872191	42876140	3p22-p21.3	3p22.1		602172	"CYP8B1, CYP12"	"Cytochrome P450, subfamily VIIIB, polypeptide 1"	CYP8B1	1582	ENSG00000180432			Cyp8b1 (MGI:1338044)			
chr3	43079228	43106084	3p22.1	3p22.1		614828	"POMGNT2, GTDC2, C3orf39, AGO61, MDDGA8"	"Protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 2"	POMGNT2	84892	ENSG00000144647		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8, 614830 (3), Autosomal recessive"	Pomgnt2 (MGI:2143424)			
chr3	43286511	43351142	3p21	3p22.1		612760	"SNRK, KIAA0096"	SNF-related kinase	SNRK	54861	ENSG00000163788			Snrk (MGI:108104)			
chr3	43366325	43691593	3p22.1	3p22.1-p21.3		613726	"ANO10, TMEM16K, SCAR10"	Anoctamin 10	ANO10	55129	ENSG00000160746		"Spinocerebellar ataxia, autosomal recessive 10, 613728 (3), Autosomal recessive"	Ano10 (MGI:2143103)			
chr3	43600000	54400000	3p21			612007	CELIAC9	"Celiac disease, susceptibility to, 9"		100188871		associated with rs6441961	"{Celiac disease, susceptibility to, 9}, 612007 (2)"				
chr3	43600000	54400000	3p21			606874	HSCR6	"Hirschsprung disease, susceptibility to, 6"		246321			"{Hirschsprung disease, susceptibility to, 6}, 606874 (2)"				
chr3	43600000	50600000	3p21.3			612241	IBD12	Inflammatory bowel disease 12		100188952			"{Inflammatory bowel disease 12}, 612241 (2)"				
chr3	43600000	74100000	3p21-p13			612574	MPVQTL2	Mean platelet volume quantitative trait locus 2		100271868		associated with rs12485738	"[Mean platelet volume QTL2], 612574 (2)"				
chr3	43600000	54400000	3p21			613806	PSC	"Cholangitis, primary sclerosing"		100653366			"Cholangitis, primary sclerosing, 613806 (2)"				
chr3	43600000	50600000	3p21.3			601994	TRR	Transfer RNA arginine		7870							
chr3	43690869	43734370	3p21	3p21.33		604780	"ABHD5, CGI58, IECN2, NCIE2"	Abhydrolase domain containing 5	ABHD5	51099	ENSG00000011198		"Chanarin-Dorfman syndrome, 275630 (3), Autosomal recessive"	Abhd5 (MGI:1914719)			
chr3	44114211	44114309	3p21.32	3p21.32		613394	"MIR138-1, MIRN138-1"	Micro RNA 138-1	MIR138-1	406929							
chr3	44200000	50600000	3p21.31			609815	ZD1	Zygodactyly 1		780914		max lod at D3S2409	"Zygodactyly 1, 609815 (2)"				
chr3	44241885	44337070	3p21.33	3p21.31		614412	"TOPAZ1, C3orf77"	Testis- and ovary-specific PAZ domain protein 1	TOPAZ1	375337	ENSG00000173769			Topaz1 (MGI:3779933)			
chr3	44648740	44660790	3p22-p21	3p21.31		194533	"ZNF35, HF10"	Zinc finger protein-35 (HF.10)	ZNF35	7584	ENSG00000169981			Zfp105 (MGI:1277119)			
chr3	44761716	44853273	3p21.31	3p21.31		617569	"KIF15, KLP2, KNSL7"	"Kinesin family, member 15"	KIF15	56992	ENSG00000163808			Kif15 (MGI:1098258)			
chr3	44874605	44914600	3p22-p21.33	3p21.31		600585	TGM4	"Transglutaminase-4, prostate"	TGM4	7047	ENSG00000163810			Tgm4 (MGI:3027002)			
chr3	44915260	44976184	3p21.31	3p21.31		617150	"ZDHHC3, DHHC3, GODZ"	Zinc finger DHHC domain-containing protein 3	ZDHHC3	51304	ENSG00000163812			Zdhhc3 (MGI:1926134)			
chr3	44975290	45012667	3p21.31	3p21.31		606488	"EXOSC7, RRP42"	Exosome component 7	EXOSC7	23016	ENSG00000075914			Exosc7 (MGI:1913696)			
chr3	45026206	45036072	3p22-p21.3	3p21.31		187520	TNA	Tetranectin (plasminogen-binding protein)	CLEC3B	7123	ENSG00000163815			Clec3b (MGI:104540)			
chr3	45082273	45146421	3p23-p21	3p21.31		611735	"CDCP1, SIMA135"	CUB domain-containing protein 1	CDCP1	64866	ENSG00000163814			Cdcp1 (MGI:2442010)			
chr3	45388563	45548841	3p21.3	3p21.31		604544	"LARS2, PRLTS4, HLASA"	"Leucyl-tRNA synthetase, mitochondrial"	LARS2	23395	ENSG00000011376	mutation identified in 1 HLASA patient	"?Hydrops, lactic acidosis, and sideroblastic anemia, 617021 (3), Autosomal recessive; Perrault syndrome 4, 615300 (3), Autosomal recessive"	Lars2 (MGI:2142973)			
chr3	45594104	45681262	3p21.3	3p21.31		604543	LIMD1	LIM domain-containing protein 1	LIMD1	8994	ENSG00000144791			Limd1 (MGI:1352502)			
chr3	45689240	45745424	3p21.3	3p21.31		606569	"SACM1L, SAC1, KIAA0851"	SAC1 suppressor of actin mutations 1-like	SACM1L	22908	ENSG00000211456			Sacm1l (MGI:1933169)			
chr3	45755448	45796552	3p21.3	3p21.31		605616	"SLC6A20, XT3"	X transporter protein 3	SLC6A20	54716	ENSG00000163817		"Hyperglycinuria, 138500 (3), Autosomal dominant; Iminoglycinuria, digenic, 242600 (3), Autosomal recessive, Digenic recessive"	Slc6a20a (MGI:2143217)			
chr3	45823315	45916036	3p21.3	3p21.31		606568	"LZTFL1, BBS17"	Leucine zipper transcription factor-like 1	LZTFL1	54585	ENSG00000163818		"Bardet-Biedl syndrome 17, 615994 (3), Autosomal recessive"	Lztfl1 (MGI:1934860)			
chr3	45886503	45903176	3p21.3	3p21.31		604738	CCR9	"Chemokine, CC motif, receptor 9"	CCR9	10803	ENSG00000173585			Ccr9 (MGI:1341902)			
chr3	45917898	45995823	3p21.3	3p21.31		607182	"FYCO1, CATC2, CTRCT18"	FYVE and coiled-coil domain containing 1	FYCO1	79443	ENSG00000163820		"Cataract 18, autosomal recessive, 610019 (3), Autosomal recessive"	Fyco1 (MGI:107277)			
chr3	45940687	45948353	3p21	3p21.31		605163	"CXCR6, STRL33, BONZO"	"Chemokine, CXC motif, receptor 6"	CXCR6	10663	ENSG00000172215			Cxcr6 (MGI:1934582)			
chr3	46016989	46086802	3p21.3-p21.1	3p21.31		600552	"XCR1, CCXCR1, GPR5"	"Chemokine, C motif, receptor 1 (G protein-coupled receptor-5)"	XCR1	2829	ENSG00000173578			Xcr1 (MGI:1346338)			
chr3	46201708	46208340	3p21	3p21.31		601159	"CCR1, CMKBR1, CKR1, HM145"	Chemokine (C-C) receptor 1	CCR1	1230	ENSG00000163823			Ccr1 (MGI:104618)			
chr3	46210698	46266705	3p21.3	3p21.31		601268	"CCR3, CKR3, CMKBR3"	Chemokine (C-C) receptor 3	CCR3	1232	ENSG00000183625			Ccr3 (MGI:104616)			
chr3	46353743	46360939	3p21	3p21.31		601267	"CCR2, CMKBR2"	Chemokine (C-C) receptor 2	CCR2	729230	ENSG00000121807		"{HIV infection, susceptibility/resistance to} (3)"	Ccr2 (MGI:106185)			
chr3	46370141	46376205	3p21	3p21.31		601373	"CCR5, CMKBR5, CCCKR5, IDDM22"	Chemokine (C-C) receptor 5	CCR5	1234	ENSG00000160791		"{Diabetes mellitus, insulin-dependent, 22}, 612522 (3); {HIV infection, susceptibility/resistance to} (3); {Hepatitis C virus, resistance to}, 609532 (3); {West nile virus, susceptibility to}, 610379 (3)"	Ccr5 (MGI:107182)			
chr3	46407165	46409522	3p21	3p21.31		608379	CCRL2	"Chemokine, CC motif, receptor-like protein 2"	CCRL2	9034	ENSG00000121797			Ccrl2 (MGI:1920904)			
chr3	46436004	46485233	3p21.31	3p21.31		150210	LTF	Lactotransferrin	LTF	4057	ENSG00000012223			Ltf (MGI:96837)			
chr3	46497994	46500948	3p21.3	3p21.31		607181	"RTP3, TMEM7"	Receptor-transporting protein 3	RTP3	83597	ENSG00000163825						
chr3	46515384	46580098	3p21.3	3p21.31		607180	LRRC2	Leucine-rich repeat-containing 2	LRRC2	79442	ENSG00000163827			Lrrc2 (MGI:1921499)			
chr3	46574554	46582462	3p23-p21	3p21.31		187395	TDGF1	Teratocarcinoma-derived growth factor-1	TDGF1	6997	ENSG00000241186		Forebrain defects (3)	Tdgf1 (MGI:98658)			
chr3	46668994	46693712	3p21.31	3p21.31		612402	ALS2CL	ALS2 C-terminal-like protein	ALS2CL	259173	ENSG00000178038			Als2cl (MGI:2447532)			
chr3	46693777	46710922	3p21	3p21.31		607237	"TMIE, DFNB6"	Transmembrane inner ear-expressed gene	TMIE	259236	ENSG00000181585		"Deafness, autosomal recessive 6, 600971 (3), Autosomal recessive"	Tmie (MGI:2159400)			
chr3	46712115	46717882	3p21.31	3p21.31		607950	PRSS50	"Protease, serine, 50"	PRSS50	29122	ENSG00000283706			Prss50 (MGI:2447303)			
chr3	46857866	46863482	3p	3p21.31		160790	"MYL3, CMH8"	"Myosin, light polypeptide-3, alkali; ventricular, skeletal, slow"	MYL3	4634	ENSG00000160808		"Cardiomyopathy, hypertrophic, 8, 608751 (3), Autosomal dominant"	Myl3 (MGI:97268)			
chr3	46877688	46903798	3p22-p21.1	3p21.31		168468	"PTHR1, PTHR, PFE"	Parathyroid hormone receptor-1	PTH1R	5745	ENSG00000160801		"Chondrodysplasia, Blomstrand type, 215045 (3), Autosomal recessive; Eiken syndrome, 600002 (3), Autosomal recessive; Failure of tooth eruption, primary, 125350 (3), Autosomal dominant; Metaphyseal chondrodysplasia, Murk Jansen type, 156400 (3), Autosomal dominant"	Pth1r (MGI:97801)			
chr3	46979682	47009703	3p22.1-p21.1	3p21.31		614169	"NBEAL2, KIAA0540, GPS, BDPLT4"	Neurobeachin-like 2	NBEAL2	23218	ENSG00000160796		"Gray platelet syndrome, 139090 (3), Autosomal recessive"	Nbeal2 (MGI:2448554)			
chr3	47016407	47164036	3p21.3-p21.2	3p21.31		612778	"SETD2, SET2, HYPB, HBP231, KIAA1732, LLS"	SET domain-containing protein 2	SETD2	29072	ENSG00000181555		"Luscan-Lumish syndrome, 616831 (3), Autosomal dominant"	Setd2 (MGI:1918177)			
chr3	47228025	47282846	3p21.31	3p21.31		607910	KIF9	Kinesin family member 9	KIF9	64147	ENSG00000088727			Kif9 (MGI:1098237)			
chr3	47380981	47413440	3p21.3	3p21.31		606584	"PTPN23, KIAA1471, HDPTP"	"Protein-tyrosine phosphatase, nonreceptor-type, 23"	PTPN23	25930	ENSG00000076201			Ptpn23 (MGI:2144837)			
chr3	47413684	47477125	3p21.31	3p21.31		601510	SCAP	SREBP cleavage-activating protein	SCAP	22937	ENSG00000114650			Scap (MGI:2135958)			
chr3	47495639	47513724	3p21.31	3p21.31		615020	"ELP6, TMEM103, C3orf75"	"Elongator acetyltransferase complex, subunit 6"	ELP6	54859	ENSG00000163832			Elp6 (MGI:1919349)			
chr3	47585887	47781914	3p23-p21	3p21.31		601732	"SMARCC1, BAF155"	"SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily C, member 1"	SMARCC1	6599	ENSG00000173473			Smarcc1 (MGI:1203524)			
chr3	47802908	47850195	3p21.31	3p21.31		616423	"DHX30, DDX30, RETCOR, KIAA0890, NEDMIAL"	DEAH box polypeptide 30	DHX30	22907	ENSG00000132153		"Neurodevelopmental disorder with severe motor impairment and absent language, 617804 (3)"	Dhx30 (MGI:1920081)			
chr3	47850689	48089278	3p21	3p21.31		157132	MAP4	Microtubule-associated protein 4	MAP4	4134	ENSG00000047849			Map4 (MGI:97178)			
chr3	48157177	48188404	3p21	3p21.31		116947	CDC25A	Cell division cycle 25A	CDC25A	993	ENSG00000164045			Cdc25a (MGI:103198)			
chr3	48223346	48225490	3p21.3	3p21.31		600474	"CAMP, FALL39"	Cathelicidin antimicrobial peptide	CAMP	820	ENSG00000164047			Camp (MGI:108443)			
chr3	48241087	48275292	3p21	3p21.31		616702	"ZNF589, SZF1"	Zinc finger protein 589	ZNF589	51385	ENSG00000164048						
chr3	48288401	48302903	3p21.3	3p21.31		608294	NME6	"Nonmetastatic cells 6, protein expressed in"	NME6	10201	ENSG00000172113			Nme6 (MGI:1861676)			
chr3	48372218	48394829	3p21	3p21.31		609075	"FBXW12, FBW12, FBXO35, FBXO12"	F-box and WD40 domain protein 12	FBXW12	285231	ENSG00000164049						
chr3	48403853	48430323	3pter-p14	3p21.31		601053	SEP	SEP transmembrane protein	PLXNB1	5364	ENSG00000164050			Plxnb1 (MGI:2154238)			
chr3	48440237	48444207	3p21.31	3p21.31		615808	"TMA7, HSPC016"	"Translation machinery-associated 7, S. cerevisiae, homolog of"	TMA7	51372	ENSG00000232112			Tma7 (MGI:1913417)			
chr3	48446709	48465654	3p21.3-p21.2	3p21.31		606605	ATRIP	ATR-interacting protein	ATRIP	84126	ENSG00000164053			Atrip (MGI:1925349)			
chr3	48465951	48467644	3p21.3-p21.2	3p21.31		606609	"TREX1, AGS1, CRV, HERNS"	3' repair exonuclease 1	TREX1	11277	ENSG00000213689		"Aicardi-Goutieres syndrome 1, dominant and recessive, 225750 (3), Autosomal recessive, Autosomal dominant; Chilblain lupus, 610448 (3), Autosomal dominant; {Systemic lupus erythematosus, susceptibility to}, 152700 (3), Autosomal dominant; Vasculopathy, retinal, with cerebral leukodystrophy, 192315 (3), Autosomal dominant"	Trex1 (MGI:1328317)			
chr3	48467797	48504825	3p21.3	3p21.31		607290	"SHISA5, SCOTIN"	"Shisa family, member 5"	SHISA5	51246	ENSG00000164054	pseudogene on Xq13.1-q13.3		Shisa5 (MGI:1915044)			
chr3	48517683	48562382	3p22-p21	3p21.31		605320	PFKFB4	"6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4"	PFKFB4	5210	ENSG00000114268			Pfkfb4 (MGI:2687284)			
chr3	48561717	48563767	3p21.3	3p21.31		605902	"UCN2, SRP, UR"	Urocortin II	UCN2	90226	ENSG00000145040			Ucn2 (MGI:2176375)			
chr3	48564072	48595301	3p21.3	3p21.31		120120	"COL7A1, NDNC8"	"Collagen VII, alpha-1 polypeptide"	COL7A1	1294	ENSG00000114270		"EBD inversa, 226600 (3), Autosomal recessive; EBD, Bart type, 132000 (3), Autosomal dominant; EBD, localisata variant (3); Epidermolysis bullosa dystrophica, AD, 131750 (3), Autosomal dominant; Epidermolysis bullosa dystrophica, AR, 226600 (3), Autosomal recessive; Epidermolysis bullosa pruriginosa, 604129 (3), Autosomal recessive, Autosomal dominant; Epidermolysis bullosa, pretibial, 131850 (3), Autosomal recessive, Autosomal dominant; Toenail dystrophy, isolated, 607523 (3), Autosomal dominant; Transient bullous of the newborn, 131705 (3), Autosomal recessive, Autosomal dominant"	Col7a1 (MGI:88462)			
chr3	48598998	48609664	3p21.3	3p21.31		191328	UQCRC1	Ubiquinol-cytochrome c reductase core protein I	UQCRC1	7384	ENSG00000010256	close upstream of COL7A1		Uqcrc1 (MGI:107876)			
chr3	48625722	48635492	3p21.3	3p21.31		610068	SLC26A6	"Solute carrier family 26 (anion transporter), member 6"	SLC26A6	65010	ENSG00000225697			Slc26a6 (MGI:2159728)			
chr3	48636462	48662914	3p24.1-p21.2	3p21.31		604264	"CELSR3, EGFL1, MEGF2"	Cadherin EGF LAG seven-pass G-type receptor 3 (epidermal growth factor-like 1)	CELSR3	1951	ENSG00000008300			Celsr3 (MGI:1858236)			
chr3	48663813	48685940	3p21	3p21.31		606671	"NCKIPSD, AF3P21, SPIN90"	NCK-interacting protein with SH3 domain	NCKIPSD	51517	ENSG00000213672			Nckipsd (MGI:1931834)			
chr3	48688002	48717277	3p21	3p21.31		606992	"IHPK2, IP6K2"	Inositol hexaphosphate kinase 2	IP6K2	51447	ENSG00000068745			Ip6k2 (MGI:1923750)			
chr3	48744600	48847849	3p21.3-p21.2	3p21.31		176910	PRKAR2A	"Protein kinase, cAMP-dependent, regulatory, type II, alpha"	PRKAR2A	5576	ENSG00000114302			Prkar2a (MGI:108025)			
chr3	48856922	48898992	3p21.31	3p21.31		613698	"SLC25A20, CACT, CAC"	"Solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 (carnitine-acylcarnitine translocase)"	SLC25A20	788	ENSG00000178537	pseudogene on 6p12	"Carnitine-acylcarnitine translocase deficiency, 212138 (3), Autosomal recessive"	Slc25a20 (MGI:1928738)			
chr3	48918819	48985540	3p21	3p21.31		605615	"ARIH2, ARI2, TRIAD1"	"Ariadne, Drosophila, homolog of, 2"	ARIH2	10425	ENSG00000177479			Arih2 (MGI:1344361)			
chr3	48989907	49007148	3p21.31	3p21.31		614584	"P4HTM, PH4"	"Prolyl 4-hydroxylase, transmembrane"	P4HTM	54681	ENSG00000178467			P4htm (MGI:1921693)			
chr3	49007061	49015952	3p21.31	3p21.31		606031	WDR6	WD repeat-containing protein 6	WDR6	11180	ENSG00000178252	previously assigned to 15q21 by FISH		Wdr6 (MGI:1930140)			
chr3	49020474	49023494	3p21.31	3p21.31		612911	NDUFAF3	"NADH dehydrogenase 1 alpha subcomplex, assembly factor 3"	NDUFAF3	25915	ENSG00000178057		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufaf3 (MGI:1913956)			
chr3	49020617	49020708	3p21.31	3p21.31		615150	MIR191	Micro RNA 191	MIR191	406966							
chr3	49024324	49029749	3p21.2	3p21.31		146691	"IMPDH2, IMPD2"	"Inosine-5'-monophosphate dehydrogenase, type II"	IMPDH2	3615	ENSG00000178035		"[IMPDH2 enzyme activity, variation in] (3)"	"Impdh2,Impdh2-ps (MGI:3705743,MGI:109367)"			
chr3	49029706	49094372	3p21.31	3p21.31		617387	QRICH1	Glutamine-rich protein 1	QRICH1	54870	ENSG00000198218			Qrich1 (MGI:1916482)			
chr3	49095931	49105128	3p21	3p21.31		603727	"QARS, GLNRS, MSCCA"	Glutaminyl-tRNA synthetase	QARS	5859	ENSG00000172053		"Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, 615760 (3), Autosomal recessive"				
chr3	49108045	49120937	3p21.31	3p21.31		614471	"USP19, KIAA0891"	Ubiquitin-specific protease 19	USP19	10869	ENSG00000172046			Usp19 (MGI:1918722)			
chr3	49121113	49133165	3p21	3p21.31		150325	"LAMB2, LAMS, NPHS5"	"Laminin, beta-2 (laminin S)"	LAMB2	3913	ENSG00000172037		"Nephrotic syndrome, type 5, with or without ocular abnormalities, 614199 (3); Pierson syndrome, 609049 (3), Autosomal recessive"	Lamb2 (MGI:99916)			
chr3	49171119	49176486	3p21.31	3p21.31		613169	"KLHDC8B, CHL"	Kelch domain-containing protein 8B	KLHDC8B	200942	ENSG00000185909		"{Hodgkin lymphoma, susceptibility to}, 236000 (3), Autosomal recessive"	Klhdc8b (MGI:1925517)			
chr3	49274119	49274185	3p21.31	3p21.31		617176	MIR4271	Micro RNA 4271	MIR4271	100422952							
chr3	49277143	49340102	3p21.31	3p21.31		603486	"USP4, UNP"	Ubiquitin-specific protease-4	USP4	7375	ENSG00000114316			Usp4 (MGI:98905)			
chr3	49357170	49358599	3p21.3	3p21.31		138320	"GPX1, GPXD"	Glutathione peroxidase-1	GPX1	2876	ENSG00000233276	?pseudogene on 3p11-p12	"Hemolytic anemia due to glutathione peroxidase deficiency, 614164 (1), Autosomal recessive"	Gpx1 (MGI:104887)			
chr3	49359135	49412096	3p21.3	3p21.31		165390	"RHOA, ARHA, ARH12, RHOH12"	"Ras homolog gene family, member A (oncogene RHO H12)"	RHOA	387	ENSG00000067560			Rhoa (MGI:1096342)			
chr3	49412205	49416475	3p21	3p21.31		600690	TCTA	T-cell leukemia translocation altered gene	TCTA	6988	ENSG00000145022			Tcta (MGI:1918829)			
chr3	49416777	49422677	3p21.2-p21.1	3p21.31		238310	"AMT, NKH, GCE"	Aminomethyltransferase (glycine cleavage system protein T)	AMT	275	ENSG00000145020		"Glycine encephalopathy, 605899 (3), Autosomal recessive"	Amt (MGI:3646700)			
chr3	49422332	49429323	3p21	3p21.31		611516	NICN1	Nicolin 1	NICN1	84276	ENSG00000145029	processed pseudogene on X		Nicn1 (MGI:1913507)			
chr3	49468702	49535617	3p21	3p21.31		128239	"DAG1, DAG, MDDGC9, MDDGA9"	Dystrophin-associated glycoprotein-1	DAG1	1605	ENSG00000173402		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9, 616538 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9, 613818 (3), Autosomal recessive"	Dag1 (MGI:101864)			
chr3	49554488	49671548	3p21.31	3p21.31		604020	"BSN, ZNF231"	"Bassoon, mouse, homolog of"	BSN	8927	ENSG00000164061			Bsn (MGI:1277955)			
chr3	49673101	49683507	3p21	3p21.31		102645	"APEH, D3S48E"	N-acylaminoacyl-peptide hydrolase	APEH	327	ENSG00000164062			Apeh (MGI:88041)			
chr3	49683946	49689522	3p21	3p21.31		142408	"MST1, HGFL"	Macrophage-stimulating-1 (hepatocyte growth factor-like)	MST1	4485	ENSG00000173531			Mst1 (MGI:96080)			
chr3	49688752	49721528	3p21.31	3p21.31		614472	"RNF123, KPC1"	Ring finger protein 123	RNF123	63891	ENSG00000164068			Rnf123 (MGI:2148796)			
chr3	49716833	49719804	3p21.31	3p21.31		615691	"AMIGO3, ALI3"	Adhesion molecule with Ig-like domain 3	AMIGO3	386724	ENSG00000176020			Amigo3 (MGI:2444854)			
chr3	49721475	49723973	3p21.31	3p21.31		615320	"GMPPB, KIAA1851, MDDGA14, MDDGB14, MDDGC14"	GDP-mannose pyrophosphorylase B	GMPPB	29925	ENSG00000173540		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14, 615350 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 14, 615351 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14, 615352 (3), Autosomal recessive"	Gmppb (MGI:2660880)			
chr3	49724294	49786539	3p21.31	3p21.31		606991	"IHPK1, IP6K1, KIAA0263"	Inositol hexaphosphate kinase 1	IP6K1	9807	ENSG00000176095			Ip6k1 (MGI:1351633)			
chr3	49805204	49813957	3p21	3p21.31		191325	"UBE7, UBE1L"	Ubiquitin-activating enzyme-7	UBA7	7318	ENSG00000182179			Uba7 (MGI:1349462)			
chr3	49828594	49856583	3p21.31	3p21.31		605958	"TRAIP, TRIP, RNF206, SCKL9"	TRAF-interacting protein	TRAIP	10293	ENSG00000183763		"Seckel syndrome 9, 616777 (3), Autosomal recessive"	Traip (MGI:1096377)			
chr3	49857980	49870221	3p21.31	3p21.31		614993	"CAMKV, 1G5"	CAM kinase-like vesicle-associated	CAMKV	79012	ENSG00000164076			Camkv (MGI:2384296)			
chr3	49886470	49903636	3p21.3	3p21.31		600168	"MST1R, RON, NPCA3"	Macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	MST1R	4486	ENSG00000164078		"{Nasopharyngeal carcinoma, susceptibility to, 3}, 617075 (3), Autosomal dominant"	Mst1r (MGI:99614)			
chr3	49908868	49930011	3p21.31	3p21.31		611464	"MON1A, SAND1"	"Mon1, S. cerevisiae, homolog of, A"	MON1A	84315	ENSG00000164077			Mon1a (MGI:1920075)			
chr3	49940040	50077251	3p21.3	3p21.31		606886	"RBM6, DEF3"	RNA-binding motif protein 6	RBM6	10180	ENSG00000004534			Rbm6 (MGI:1338037)			
chr3	50088907	50118963	3p21.3	3p21.31		606884	"RMB5, LUCA15"	RNA-binding motif protein 5	RBM5	10181	ENSG00000003756			Rbm5 (MGI:1933204)			
chr3	50155044	50189074	3p21.3	3p21.31		601124	"SEMA3F, SEMA4"	Semaphorin III/F	SEMA3F	6405	ENSG00000001617			Sema3f (MGI:1096347)			
chr3	50191609	50197695	3p21	3p21.31		139330	"GNAT1, CSNBAD3, CSNB1G"	"Guanine nucleotide-binding protein (G protein), alpha-transducing (transducin) activity polypeptide-1"	GNAT1	2779	ENSG00000114349		"Night blindness, congenital stationary, autosomal dominant 3, 610444 (3), Autosomal dominant; Night blindness, congenital stationary, type 1G, 616389 (3), Autosomal recessive"	Gnat1 (MGI:95778)			
chr3	50205245	50221485	3p21.3	3p21.31		604437	"SLC38A3, SN1, G17"	"Solute carrier family 38, member 3"	SLC38A3	10991	ENSG00000188338			Slc38a3 (MGI:1923507)			
chr3	50226687	50259353	3p21	3p21.31		139360	"GNAI2, GNAI2B, GIP"	"Guanine nucleotide-binding protein (G protein), alpha-inhibiting activity polypeptide-2"	GNAI2	2771	ENSG00000114353	"on 12p13-p12, GNAI2L"	"Pituitary ACTH-secreting adenoma (3); Ventricular tachycardia, idiopathic, 192605 (3), Autosomal dominant"	Gnai2 (MGI:95772)			
chr3	50267557	50277170	3p21.3	3p21.31		601281	SEMA5	Semaphorin A(V)	SEMA3B	7869	ENSG00000012171			Sema3b (MGI:107561)			
chr3	50287731	50292594	3p21.3	3p21.31		602725	IFRD2	Interferon-related developmental regulator-2	IFRD2	7866	ENSG00000214706			Ifrd2 (MGI:1316708)			
chr3	50292827	50299467	3p21.3	3p21.31		604038	"HYAL3, LUCA3"	Hyaluronoglucosaminidase 3	HYAL3	8372	ENSG00000186792			Hyal3 (MGI:1330288)			
chr3	50296401	50299420	3p21.3	3p21.31		607073	FUS2	FUS2 gene	NAT6	24142	ENSG00000243477			Nat6 (MGI:1888902)			
chr3	50299888	50312950	3p21.3-p21.2	3p21.31		607071	"HYAL1, MPS9"	Hyaluronoglucosaminidase 1	HYAL1	3373	ENSG00000114378	mutation identified in 1 MPS9 patient	"?Mucopolysaccharidosis type IX, 601492 (3), Autosomal recessive"	Hyal1 (MGI:96298)			
chr3	50317789	50322849	3p21.3	3p21.31		603551	"HYAL2, LUCA2"	Hyaluronoglucosaminidase 2	HYAL2	8692	ENSG00000068001			Hyal2 (MGI:1196334)			
chr3	50324908	50328237	3p21.3	3p21.31		607052	FUS1	FUS1 gene	TUSC2	11334	ENSG00000114383			Tusc2 (MGI:1931086)			
chr3	50329785	50340935	3p21.3	3p21.31		605082	RASSF1	RAS association domain family protein 1	RASSF1	11186	ENSG00000068028	epigenetically inactivated	"Lung cancer, 211980 (2), Autosomal recessive"	Rassf1 (MGI:1928386)			
chr3	50341105	50345745	3p21.3	3p21.31		607070	"ZMYND10, BLU"	Zinc finger MYND domain-containing protein 10	ZMYND10	51364	ENSG00000004838		"Ciliary dyskinesia, primary, 22, 615444 (3), Autosomal recessive"	Zmynd10 (MGI:2387863)			
chr3	50347486	50351054	3p21.3	3p21.31		607072	"NPR2L, NPRL2, FFEVF2"	"Npr2, S. cerevisiae, homolog of"	NPRL2	10641	ENSG00000114388		"Epilepsy, familial focal, with variable foci 2, 617116 (3), Autosomal dominant"	Nprl2 (MGI:1914482)			
chr3	50350694	50368196	3p21.3	3p21.31		607068	"CYB561D2, 101F6"	Cytochrome b-561 domain containing 2	CYB561D2	11068	ENSG00000114395			Cyb561d2 (MGI:1929280)			
chr3	50354748	50359507	3p21.3	3p21.31		607069	"TMEM115, PL6"	Transmembrane protein 115	TMEM115	11070	ENSG00000126062						
chr3	50362612	50504243	3p21.3	3p21.31		607082	"CACNA2D2, KIAA0558"	"Calcium channel, voltage-dependent, alpha-2/delta subunit 2"	CACNA2D2	9254	ENSG00000007402			Cacna2d2 (MGI:1929813)			
chr3	50606453	50611830	3p21.3	3p21.2		602441	"CISH, BACTS2"	Cytokine inducible SH2-containing protein	CISH	1154	ENSG00000114737		"{Bacteremia, susceptibility to}, 614383 (3); {Malaria, susceptibility to}, 611162 (3); {Tuberculosis, susceptibility to}, 607948 (3)"	Cish (MGI:103159)			
chr3	50611861	50649296	3p21.3	3p21.2		602130	"MAPKAP3, 3PK, MDPT3"	Mitogen-activated protein kinase-activated protein kinase-3	MAPKAPK3	7867	ENSG00000114738	mutation identified in 1 MDPT3 family	"?Macular dystrophy, patterned, 3, 617111 (3), Autosomal dominant"	Mapkapk3 (MGI:2143163)			
chr3	50674968	51384197	3p14	3p21.2		603123	DOCK3	Dedicator of cytokinesis 3	DOCK3	1795	ENSG00000088538			Dock3 (MGI:2429763)			
chr3	51385236	51389396	3p21.1	3p21.2		601916	"ARMET, ARP"	"Arginine-rich protein, mutated in early stage tumors"	MANF	7873	ENSG00000145050			Manf (MGI:1922090)			
chr3	51391267	51397907	3p21.1	3p21.2		612602	"RBM15B, OTT3, HUMAGCGB"	RNA-binding motif protein 15B	RBM15B	29890	ENSG00000259956			Rbm15b (MGI:1923598)			
chr3	51394260	51505619	3p21.2	3p21.2		617259	"DCAF1, RIP, VPRBP, KIAA0800"	DDB1- and CUL4-associated factor 1	DCAF1	9730	ENSG00000145041			Dcaf1 (MGI:2445220)			
chr3	51707032	51718615	3p21.2-p21.1	3p21.2		604099	"GRM2, MGLUR2"	"Glutamate receptor, metabotropic, 2"	GRM2	2912	ENSG00000164082			Grm2 (MGI:1351339)			
chr3	51942276	51948866	3p21.3-p21.1	3p21.2		607726	"PARP3, ADPRTL3"	Poly(ADP-ribose) polymerase 3	PARP3	10039	ENSG00000041880			Parp3 (MGI:1891258)			
chr3	51955313	51957503	3p21.1	3p21.2		606917	GPR62	G protein-coupled receptor 62	GPR62	118442	ENSG00000180929			Gpr62 (MGI:3525078)			
chr3	51957453	51967465	3p21.2	3p21.2		608503	"PCBP4, MGC10"	Poly(rC)-binding protein 4	PCBP4	57060	ENSG00000090097			Pcbp4 (MGI:1890471)			
chr3	51983283	51989201	3p21.1	3p21.2		104620	"ACY1, ACY1D"	Aminoacylase-1	ACY1	95	ENSG00000243989		"Aminoacylase 1 deficiency, 609924 (3), Autosomal recessive"	Acy1 (MGI:87913)			
chr3	51993606	51995941	3q29-qter	3p21.2		601832	"RPL29, HIP"	Ribosomal protein L29	RPL29	6159	ENSG00000162244						
chr3	52048918	52056444	3p21	3p21.2		602749	"DUSP7, MKPX, PYST2"	Dual-specificity phosphatase-7	DUSP7	1849	ENSG00000164086			Dusp7 (MGI:2387100)			
chr3	52075232	52154689	3p21.2	3p21.2		614783	"POC1A, PIX2, SOFT"	"POC1 centriolar protein, Chlamydomonas, homolog of, A"	POC1A	25886	ENSG00000164087		"Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis, 614813 (3), Autosomal recessive"	Poc1a (MGI:1917485)			
chr3	52198082	52214326	3p21.1	3p21.2		125290	ALAS1	"Aminolevulinate, delta-, synthase-1"	ALAS1	211	ENSG00000023330			Alas1 (MGI:87989)			
chr3	52221079	52226162	3p21.3	3p21.2		605474	TLR9	Toll-like receptor 9	TLR9	54106	ENSG00000239732			Tlr9 (MGI:1932389)			
chr3	52228609	52239166	3p21.1	3p21.2		607433	"TWF2, PTK9L, A6RP"	"Twinfilin, actin-binding protein, Drosophila, homolog of, 2"	TWF2	11344	ENSG00000247596			Twf2 (MGI:1346078)			
chr3	52245724	52250598	3p21.2	3p21.2		608979	"PPM1M, PP2CE"	"Protein phosphatase 1M (protein phosphatase 2C, eta isoform)"	PPM1M	132160	ENSG00000164088			Ppm1m (MGI:1915155)			
chr3	52254421	52278642	3p21.1	3p21.2		611059	"WDR82, TMEM113"	WD repeat-containing protein 82	WDR82	80335	ENSG00000164091			Wdr82 (MGI:1924555)			
chr3	52268277	52268360	3p21.1	3p21.2		612102	"MIRLET7G, LET7G, MIRNLET7G"	Micro RNA Let7G	MIRLET7G	406890							
chr3	52287557	52295255	3p21	3p21.2		610516	"GLYCTK, GLYCTK1"	Glycerate kinase	GLYCTK	132158	ENSG00000168237		"D-glyceric aciduria, 220120 (3), Autosomal recessive"	Glyctk (MGI:2444085)			
chr3	52313009	52400496	3p21.3	3p21.1		603332	"DNAH1, HL11, DNAHC1, HDHC7, SPGF18, CILD37"	"Dynein, axonemal, heavy chain-1"	DNAH1	25981	ENSG00000114841	mutation identified in 1 CILD37 family	"?Ciliary dyskinesia, primary, 37, 617577 (3), Autosomal recessive; Spermatogenic failure 18, 617576 (3), Autosomal recessive"	Dnah1 (MGI:107721)			
chr3	52401003	52410104	3p21.3	3p21.1		603089	"BAP1, TPDS"	BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)	BAP1	8314	ENSG00000163930		"Tumor predisposition syndrome, 614327 (3), Autosomal dominant"	Bap1 (MGI:1206586)			
chr3	52451090	52454040	3p21.3-p14.3	3p21.1		191040	"TNNC1, CMD1Z, CMH13"	"Troponin-C1, slow"	TNNC1	7134	ENSG00000114854		"Cardiomyopathy, dilated, 1Z, 611879 (3); Cardiomyopathy, hypertrophic, 13, 613243 (3), Autosomal dominant"	Tnnc1 (MGI:98779)			
chr3	52455507	52493071	3p21.1	3p21.1		615507	"NISCH, IRAS, KIAA0975"	Nischarin	NISCH	11188	ENSG00000010322						
chr3	52545351	52685906	3p21	3p21.1		606083	"PBRM1, PB1, BAF180"	"Polybromo 1, chicken, homolog of"	PBRM1	55193	ENSG00000163939			Pbrm1 (MGI:1923998)			
chr3	52685919	52694496	3p21.1	3p21.1		608011	"GNL3, NS, E2IG3"	Guanine nucleotide-binding protein-like 3	GNL3	26354	ENSG00000163938			Gnl3 (MGI:1353651)			
chr3	52705840	52708181	3p21.1	3p21.1		610358	"SPCS1, SPC12"	"Signal peptidase complex, subunit 1, S. cerevisiae, homolog of"	SPCS1	28972	ENSG00000114902			Spcs1 (MGI:1916269)			
chr3	52708448	52770948	3p21.1	3p21.1		601959	"NEK4, STK2, NRK2"	NIMA (never in mitosis gene a)-related kinase 4 (serine/threonine protein kinase-2)	NEK4	6787	ENSG00000114904			Nek4 (MGI:1344404)			
chr3	52777585	52792067	3p21.2-p21.1	3p21.1		147270	ITIH1	"Inter-alpha (globulin) inhibitor, H1 polypeptide"	ITIH1	3697	ENSG00000055957			Itih1 (MGI:96618)			
chr3	52794767	52809008	3p21.2-p21.1	3p21.1		146650	ITIH3	"Inter-alpha (globulin) inhibitor, H3 polypeptide"	ITIH3	3699	ENSG00000162267			Itih3 (MGI:96620)			
chr3	52812989	52830700	3p21.2-p14.1	3p21.1		600564	"ITIH4, PK120, ITIHL1"	"Inter-alpha (globulin) inhibitor, H4 polypeptide"	ITIH4	3700	ENSG00000055955		"{Hypercholesterolemia, susceptibility to}, 143890 (3), Autosomal dominant"	Itih4 (MGI:109536)			
chr3	52833114	52835218	3p21.1	3p21.1		617195	"MUSTN1, MUSTANG"	Musculoskeletal embryonic nuclear protein 1	MUSTN1	389125	ENSG00000272573			Mustn1 (MGI:1913425)			
chr3	52836755	52897580	3p21.1	3p21.1		617189	"TMEM110, STIMATE"	Transmembrane protein 110	STIMATE	375346	ENSG00000213533						
chr3	52899208	53046654	3p21.1	3p21.1		607319	"SFMBT1, RU1"	SCM-like protein with 4 MBT domains 1	SFMBT1	51460	ENSG00000163935			Sfmbt1 (MGI:1859609)			
chr3	53071150	53130468	3p21.1	3p21.1		611908	"RFT1, CDG1N"	"RFT1, S. cerevisiae, homolog of"	RFT1	91869	ENSG00000163933		"Congenital disorder of glycosylation, type In, 612015 (3), Autosomal recessive"	Rft1 (MGI:3607791)			
chr3	53161206	53192716	3p	3p21.1		176977	"PRKCD, CVID9, ALPS3"	"Protein kinase C, delta"	PRKCD	5580	ENSG00000163932	mutation identified in 1 family	"Autoimmune lymphoproliferative syndrome, type III, 615559 (3), Autosomal recessive"	Prkcd (MGI:97598)			
chr3	53224706	53256113	3p14.3	3p21.1		606781	"TKT, SDDHD"	Transketolase	TKT	7086	ENSG00000163931		"Short stature, developmental delay, and congenital heart defects, 617044 (3), Autosomal recessive"	Tkt (MGI:105992)			
chr3	53283422	53347626	3p21.1	3p21.1		607010	"DCP1A, SMIF"	"Decapping enzyme 1, X. cerevisiae, homolog of, A"	DCP1A	55802	ENSG00000272886			Dcp1a (MGI:1923151)			
chr3	53495048	53813150	3p21.1	3p21.1		114206	"CACNA1D, CACNL1A2, CCHL1A2, SANDD, PASNA"	"Calcium channel, voltage-dependent, L type, alpha 1D subunit"	CACNA1D	776	ENSG00000157388		"Primary aldosteronism, seizures, and neurologic abnormalities, 615474 (3), Autosomal dominant; Sinoatrial node dysfunction and deafness, 614896 (3), Autosomal recessive"	Cacna1d (MGI:88293)			
chr3	53846549	53867387	3p21.1	3p21.1		605458	"IL17RB, IL17BR, IL17RH1"	"Interleukin 17, receptor B"	IL17RB	55540	ENSG00000056736			Il17rb (MGI:1355292)			
chr3	53884975	53892014	3p21.31	3p21.1		607916	"SELENOK, SELK, HSPC030"	Selenoprotein K	SELENOK	58515	ENSG00000113811			Selenok (MGI:1931466)			
chr3	54122593	55074556	3p21.1	3p21.1-p14.3		606399	CACNA2D3	"Calcium channel, voltage-dependent, alpha-2/delta subunit 3"	CACNA2D3	55799	ENSG00000157445			Cacna2d3 (MGI:1338890)			
chr3	54400000	122200000	3p14-q13			608586	KTCN3	Keratoconus 3		406215			"Keratoconus 3, 608586 (2)"				
chr3	54632123	54639856	3p14.3	3p14.3		611473	HESRG	Embryonic stem cell-related protein	ESRG	790952							
chr3	55465714	55505260	3p21-p14	3p14.3		164975	WNT5A	"Wingless-type MMTV integration site family, member 5A"	WNT5A	7474	ENSG00000114251		"Robinow syndrome, autosomal dominant 1, 180700 (3), Autosomal dominant"	Wnt5a (MGI:98958)			
chr3	55508310	56468472	3p14.3	3p14.3		617250	"ERC2, CAST, KIAA0378"	"ELKS/RAB6-interacting/CAST family, member 2"	ERC2	26059	ENSG00000187672			Erc2 (MGI:1098749)			
chr3	56620131	56683236	3p14.3	3p14.3		616493	"FAM208A, RAP140, C3orf63, KIAA1105"	"Family with sequence similarity 208, member A"	FAM208A	23272	ENSG00000163946			Fam208a (MGI:1921694)			
chr3	56727417	57079307	3p21-p13	3p14.3		612115	"ARHGEF3, XPLN"	RHO guanine nucleotide exchange factor 3	ARHGEF3	50650	ENSG00000163947			Arhgef3 (MGI:1918954)			
chr3	57060440	57075431	3p21.2-p21.1	3p14.3		609869	"SPATA12, SRG5"	Spermatogenesis-associated protein 12	SPATA12	353324	ENSG00000186451						
chr3	57089981	57170316	3p14.3-p14.2	3p14.3		606807	"IL17RD, SEF, HH18"	"Interleukin 17, receptor D (Sef, zebrafish, homolog of)"	IL17RD	54756	ENSG00000144730		"Hypogonadotropic hypogonadism 18 with or without anosmia, 615267 (3), Autosomal recessive, Autosomal dominant"	Il17rd (MGI:2159727)			
chr3	57197837	57227642	3p21.2-p21.1	3p14.3		601802	"HESX1, RPX, CPHD5"	Homeo box gene expressed in ES cells	HESX1	8820	ENSG00000163666		"Growth hormone deficiency with pituitary anomalies, 182230 (3), Autosomal recessive, Autosomal dominant; Pituitary hormone deficiency, combined, 5, 182230 (3), Autosomal recessive, Autosomal dominant; Septooptic dysplasia, 182230 (3), Autosomal recessive, Autosomal dominant"	Hesx1 (MGI:96071)			
chr3	57227736	57273470	3p21.1-p14.3	3p14.3		604299	"APPL1, APPL, MODY14"	"Adaptor protein containing PH domain, PTB domain, and leucine zipper motif 1"	APPL1	26060	ENSG00000157500		"{Maturity-onset diabetes of the young, type 14}, 616511 (3), Autosomal dominant"	Appl1 (MGI:1920243)			
chr3	57293698	57545202	3p21.1	3p14.3		603340	"DNAH12, DNAHC3, HL19"	"Dynein, heavy chain-5"	DNAH12	201625	ENSG00000174844			Dnah12 (MGI:107720)			
chr3	57556246	57656479	3q21.2	3p14.3		616519	PDE12	Phosphodiesterase 12	PDE12	201626	ENSG00000174840			Pde12 (MGI:2443226)			
chr3	57571362	57597487	3p14.1	3p14.3		601177	"ARF4, ARF2"	ADP-ribosylation factor 4	ARF4	378	ENSG00000168374			Arf4 (MGI:99433)			
chr3	57756228	57930012	3p21.2-p14.3	3p14.3		602701	SLAP	Sarcolemmal-associated protein	SLMAP	7871	ENSG00000163681			Slmap (MGI:1933549)			
chr3	58008399	58172254	3p14.3	3p14.3		603381	"FLNB, SCT, AOI, LRS1"	Filamin B	FLNB	2317	ENSG00000136068		"Atelosteogenesis, type I, 108720 (3), Autosomal dominant; Atelosteogenesis, type III, 108721 (3), Autosomal dominant; Boomerang dysplasia, 112310 (3), Autosomal dominant; Larsen syndrome, 150250 (3), Autosomal dominant; Spondylocarpotarsal synostosis syndrome, 272460 (3), Autosomal recessive"	Flnb (MGI:2446089)			
chr3	58192625	58211002	3p21.1-p14.3	3p14.3		602244	"DNASE1L3, SLEB16"	Deoxyribonuclease I-like 3	DNASE1L3	1776	ENSG00000163687		"Systemic lupus erythematosus 16, 614420 (3), Autosomal recessive"	Dnase1l3 (MGI:1314633)			
chr3	58237501	58294735	3p14.3	3p14.3		616966	ADHB6	Abhydrolase domain-containing protein 6	ABHD6	57406	ENSG00000163686			Abhd6 (MGI:1913332)			
chr3	58306244	58320192	3p14.3	3p14.3		606112	RPP14	"Ribonuclease P, 14kD subunit"	RPP14	11102	ENSG00000163684			Rpp14 (MGI:1914303)			
chr3	58332889	58426126	3p14.3	3p14.3		611450	"PXK, MONAKA"	PXK domain-containing serine/threonine kinase	PXK	54899	ENSG00000168297			Pxk (MGI:1289230)			
chr3	58427629	58433851	3p13-q23	3p14.3		179060	"PDHB, PDHBD"	"Pyruvate dehydrogenase, E1 beta polypeptide"	PDHB	5162	ENSG00000168291		"Pyruvate dehydrogenase E1-beta deficiency, 614111 (3)"	Pdhb (MGI:1915513)			
chr3	58505135	58537201	3p14.3	3p14.3		601641	"ACOX2, BRCACOX, CBAS6"	"Acyl-Coenzyme A oxidase 2, branched chain"	ACOX2	8309	ENSG00000168306		"Bile acid synthesis defect, congenital, 6, 617308 (3), Autosomal recessive"	Acox2 (MGI:1934852)			
chr3	58564111	58627609	3p21.1	3p14.3-p14.2		608295	"FAM107A, DRR1, TU3A"	"Family with sequence similarity 107, member A (downregulated in renal cell carcinoma 1)"	FAM107A	11170	ENSG00000168309			Fam107a (MGI:3041256)			
chr3	58633942	58666842	3p14.2	3p14.2		608619	FAM3D	"Family with sequence similarity 3, member D"	FAM3D	131177	ENSG00000198643			Oit1 (MGI:1201784)			
chr3	59747277	61251473	3p14.2	3p14.2		601153	"FRA3B, FHIT"	Fragile histidine triad gene	FHIT	2272	ENSG00000189283	deleted in RCC		Fhit (MGI:1277947)			
chr3	61561568	62297608	3p14.2	3p14.2		176886	"PTPRG, PTPG"	"Protein tyrosine phosphatase, receptor type, gamma polypeptide"	PTPRG	5793	ENSG00000144724			Ptprg (MGI:97814)			
chr3	62369671	62373514	3p14.2	3p14.2		607414	"FEZF2, ZNF312, FEZL, TOF"	FEZ family zinc finger 2	FEZF2	55079	ENSG00000153266			Fezf2 (MGI:1859823)			
chr3	62398345	62875864	3p21.1	3p14.2		604667	"CADPS, CAPS"	Ca(2+)-dependent activator protein for secretion	CADPS	8618	ENSG00000163618			Cadps (MGI:1350922)			
chr3	63652667	63665216	3p14.2	3p14.2		617832	"SNTN, S100AL, S100A1L"	"Sentan, cilia apical structural protein"	SNTN	132203	ENSG00000188817			Sntn (MGI:3045373)			
chr3	63800000	103100000	3p14.1-q12.3			610948	HYT7	"Hypertension, essential, susceptibility to, 7"		100188825			"{Hypertension, essential, susceptibility to, 7}, 610948 (2)"				
chr3	63833869	63864477	3p14.1	3p14.1		611965	"THOC7, NIF3L1BP1"	"THO complex, subunit 7"	THOC7	80145	ENSG00000163634			Thoc7 (MGI:1913481)			
chr3	63864556	64003461	3p14.1	3p14.1		607640	"ATXN7, SCA7, OPCA3"	Ataxin 7	ATXN7	6314	ENSG00000163635		"Spinocerebellar ataxia 7, 164500 (3), Autosomal dominant"	Atxn7 (MGI:2179277)			
chr3	63911517	63911771	3p14.1	3p14.1		614481	"ATXN7AS1, SCAANT1"	ATXN7 antisense noncoding transcript 1	SCAANT1	100861563							
chr3	64010548	64024009	3p14.1	3p14.1		617857	"PSMD6, KIAA0107"	"Proteasome 26S subunit, non-ATPase, 6"	PSMD6	9861	ENSG00000163636			Psmd6 (MGI:1913663)			
chr3	64093849	64445475	3p14	3p14.1		608501	PRICKLE2	Prickle-like 2	PRICKLE2	166336	ENSG00000163637			Prickle2 (MGI:1925144)			
chr3	64515653	64687999	3p14.3-p14.2	3p14.1		605421	ADAMTS9	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 9"	ADAMTS9	56999	ENSG00000163638			Adamts9 (MGI:1916320)			
chr3	65354230	66038833	3p14.1	3p14.1		602625	"MAGI1, BAIAP1, WWP3, TNRC19"	"Membrane-associated guanylate kinase, WW and PDZ domains-containing, 1"	MAGI1	9223	ENSG00000151276			Magi1 (MGI:1203522)			
chr3	66133609	66380020	3p14.3	3p14.1		611037	"SLC25A26, SAMC, COXPD28"	"Solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26"	SLC25A26	115286	ENSG00000144741		"Combined oxidative phosphorylation deficiency 28, 616794 (3), Autosomal recessive"	Slc25a26 (MGI:1914832)			
chr3	66378796	66501262	3p14	3p14.1		608868	"LRIG1, LIG1"	Leucine-rich repeats- and immunoglobulin-like domains-containing protein 1	LRIG1	26018	ENSG00000144749			Lrig1 (MGI:107935)			
chr3	66998302	67011209	3p14.1	3p14.1		616607	"KBTBD8, TAKRP, KIAA1842"	KELCH repeat- and BTB/POZ domain-containing protein 8	KBTBD8	84541	ENSG00000163376			Kbtbd8 (MGI:2661430)			
chr3	67360459	67654613	3p14.1	3p14.1		603922	SUCLG2	"Succinate-CoA ligase, GDP-forming, beta subunit"	SUCLG2	8801	ENSG00000172340			Suclg2 (MGI:1306824)			
chr3	67991591	68546055	3p14.1	3p14.1		617495	"FAM19A1, TAFA1"	"Family with sequence similarity 19, member A1, CC motif chemokine-like"	FAM19A1	407738	ENSG00000183662			Fam19a1 (MGI:2443695)			
chr3	68731763	68932609	3p14.1	3p14.1		617498	"FAM19A4, TAFA4"	"Family with sequence similarity 19, member A4, CC motif chemokine-like"	FAM19A4	151647	ENSG00000163377			Fam19a4 (MGI:2444563)			
chr3	68975211	69013960	3p14.1	3p14.1		614789	"EOGT, EOGT1, C3orf64, AOS4"	EGF domain-specific O-linked N-acetylglucosamine transferase	EOGT	285203	ENSG00000163378		"Adams-Oliver syndrome 4, 615297 (3), Autosomal recessive"	Eogt (MGI:2141669)			
chr3	69019826	69052332	3p21-p12	3p14.1		601126	TMF1	TATA element modulatory factor 1	TMF1	7110	ENSG00000144747			Tmf1 (MGI:2684999)			
chr3	69084938	69106087	3p14	3p14.1		605709	ARL6IP5	ADP-ribosylation-like factor 6-interacting protein 5	ARL6IP5	10550	ENSG00000144746			Arl6ip5 (MGI:1929501)			
chr3	69108671	69122594	3p14.1	3p14.1		616112	"LMOD3, NEM10"	Leiomodin 3	LMOD3	56203	ENSG00000163380		"Nemaline myopathy 10, 616165 (3), Autosomal recessive"	Lmod3 (MGI:2444169)			
chr3	69168781	69541339	3p14.1	3p14.1		617467	"FRMD4B, GRSP1, KIAA1013"	FERM domain-containing protein 4B	FRMD4B	23150	ENSG00000114541			Frmd4b (MGI:2141794)			
chr3	69739434	69968336	3p14.1-p12.3	3p13		156845	"MITF, WS2A, CMM8, COMMAD"	Microphthalmia-associated transcription factor	MITF	4286	ENSG00000187098		"COMMAD syndrome, 617306 (3), Autosomal recessive; {Melanoma, cutaneous malignant, susceptibility to, 8}, 614456 (3); Tietz albinism-deafness syndrome, 103500 (3), Autosomal dominant; Waardenburg syndrome, type 2A, 193510 (3), Autosomal dominant; Waardenburg syndrome/ocular albinism, digenic, 103470 (3), Autosomal dominant"	Mitf (MGI:104554)			
chr3	69999743	70015300	3p13	3p13		616895	"SAMMSON, LINC01212"	Survival-associated mitochondrial melanoma-specific oncogenic noncoding RNA	SAMMSON	101927152							
chr3	70954713	71583988	3p14.1	3p13		605515	"FOXP1, QRF1"	Forkhead box P1	FOXP1	27086	ENSG00000114861		"Mental retardation with language impairment and with or without autistic features, 613670 (3), Autosomal dominant"				
chr3	71679288	71754772	3p14	3p13		609896	EIF4E3	"Eukaryotic translation initiation factor 4E family, member 3"	EIF4E3	317649	ENSG00000163412			Eif4e3 (MGI:1914142)			
chr3	71753723	71756379	3p21-p14	3p13		605187	"GPR27, SREB1"	G protein-coupled receptor 27	GPR27	2850	ENSG00000170837			Gpr27 (MGI:1202299)			
chr3	71771654	71785205	3p21.1	3p13		607002	"PROK2, PK2, BV8, HH4"	Prokineticin 2	PROK2	60675	ENSG00000163421		"Hypogonadotropic hypogonadism 4 with or without anosmia, 610628 (3), Autosomal dominant"	Prok2 (MGI:1354178)			
chr3	72374592	72446622	3p13	3p13		607535	"RYBP, YEAF1"	Ring1- and YY1-binding protein	RYBP	23429				"Rybp,Rybp-ps (MGI:3648043,MGI:1929059)"			
chr3	72725701	72848474	3p13	3p13		613663	SHQ1	"Shq1, S. cerevisiae, homolog of"	SHQ1	55164	ENSG00000144736			Shq1 (MGI:1919421)			
chr3	72848521	72976916	3p13	3p13		613322	"GXYLT2, GLT8D4"	Glucoside xylosyltransferase 2	GXYLT2	727936	ENSG00000172986			Gxylt2 (MGI:2682940)			
chr3	72996742	73069200	3p13	3p13		613822	"PPP4R2, PP4R2"	"Protein phosphatase 4, regulatory subunit 2"	PPP4R2	151987	ENSG00000163605			Ppp4r2 (MGI:3027896)			
chr3	73061658	73063336	3p14-p13	3p13		613250	EBLN2	Endogenous Borna-like N element-containing protein 2	EBLN2	55096	ENSG00000255423						
chr3	73382429	73624996	3p13	3p13		609729	"PDZRN3, KIAA1095"	PDZ domain-containing ring finger protein 3	PDZRN3	23024	ENSG00000121440			Pdzrn3 (MGI:1933157)			
chr3	74100000	122200000	3p12-q13			606896	DYX5	"Dyslexia, susceptibility to, 5"	DYX5	171089		?same locus as SSD	"{Dyslexia, susceptibility to, 5}, 606896 (2)"				
chr3	74100000	113700000	3p12-q13.2			109720	PBC1	"Biliary cirrhosis, primary, 1"				associated with rs6441286	"Biliary cirrhosis, primary, 1, 109720 (2), Autosomal dominant"				
chr3	74100000	122200000	3p12-q13			608445	SSD	Speech-sound disorder		404713		?same locus as DYX5	"{Speech-sound disorder}, 608445 (2)"				
chr3	74262567	74614447	3p26	3p12.3		601325	"CNTN3, PANG"	Contactin 3 (plasmocytoma-associated neuronal glycoprotein)	CNTN3	5067	ENSG00000113805			Cntn3 (MGI:99534)			
chr3	75906674	77649963	3p12.3	3p12.3		602431	"ROBO2, SAX3, KIAA1568"	"Roundabout, Drosophila, homolog of, 2"	ROBO2	6092	ENSG00000185008		"Vesicoureteral reflux 2, 610878 (3)"	Robo2 (MGI:1890110)			
chr3	78597237	79767997	3p12	3p12.3		602430	"ROBO1, DUTT1, SAX3"	"Roundabout, Drosophila, homolog of, 1"	ROBO1	6091	ENSG00000169855			Robo1 (MGI:1274781)			
chr3	81489698	81761798	3p12	3p12.2		607839	"GBE1, GSD4, APBD"	Glycogen branching enzyme	GBE1	2632			"Glycogen storage disease IV, 232500 (3), Autosomal recessive; Polyglucosan body disease, adult form, 263570 (3), Autosomal recessive"	Gbe1 (MGI:1921435)			
chr3	84958981	86074428	3p12	3p12.1		609938	"CADM2, IGSF4D, SYNCAM2, NECL3"	Cell adhesion molecule 2	CADM2	253559	ENSG00000175161			Cadm2 (MGI:2442722)			
chr3	86937968	86991122	3p12.1	3p12.1		609980	"VGLL3, VGL3"	Vestigial-like 3	VGLL3	389136	ENSG00000206538			Vgll3 (MGI:1920819)			
chr3	87227262	87255547	3p11.2	3p11.2		609512	"CHMP2B, DMT1, VPS2B, ALS17"	"CHMP family, member 2B"	CHMP2B	25978	ENSG00000083937		"Amyotrophic lateral sclerosis 17, 614696 (3), Autosomal dominant; Dementia, familial, nonspecific, 600795 (3), Autosomal dominant"	Chmp2b (MGI:1916192)			
chr3	87259632	87276586	3p11	3p11.2		173110	"POU1F1, PIT1, CPHD1"	"POU domain, class 1, transcription factor 1 (Pit1, growth hormone factor 1)"	POU1F1	5449	ENSG00000064835		"Pituitary hormone deficiency, combined, 1, 613038 (3), Autosomal recessive, Autosomal dominant"	Pou1f1 (MGI:97588)			
chr3	87792766	87994855	3p12	3p11.2-p11.1		182134	"HTR1F, HTR1EL, MR77"	5-hydroxytryptamine receptor 1F	HTR1F	3355	ENSG00000179097			Htr1f (MGI:99842)			
chr3	88051949	88149865	3p12-p11.1	3p11.1		603363	CGGBP1	CGG triplet repeat binding protein 1	CGGBP1	8545	ENSG00000163320			Cggbp1 (MGI:2146370)			
chr3	89107523	89482133	3p11.2	3p11.1		179611	"EPHA3, ETK1, HEK"	Ephrin receptor EphA3 (human embryo kinase 1)	EPHA3	2042	ENSG00000044524			Epha3 (MGI:99612)			
chr3	90900000	122200000	3cen-q13			614012	"ERVK-5, HERV-KII"	"Endogenous retrovirus group K, member 5"	ERVK-5	60358							
chr3	93873036	93974089	3q11.2	3q11.1		176880	"PROS1, THPH5, THPH6"	"Protein S, alpha"	PROS1	5627	ENSG00000184500	pseudogene PROSP contiguous on chr.3	"Thrombophilia due to protein S deficiency, autosomal dominant, 612336 (3), Autosomal dominant; Thrombophilia due to protein S deficiency, autosomal recessive, 614514 (3), Autosomal recessive"	Pros1 (MGI:1095733)			
chr3	93980138	94055677	3q11.2	3q11.1-q11.2		608922	"ARL13B, ARL2L1, JBTS8"	ADP-ribosylation factor-like 13B	ARL13B	200894	ENSG00000169379		"Joubert syndrome 8, 612291 (3), Autosomal recessive"	Arl13b (MGI:1915396)			
chr3	94000000	108200000	3q11.2-q13.12			114200	CAMPD1	Camptodactyly 1		100381210		between D3S2465 and D3S3044	"Camptodactyly 1, 114200 (2), Autosomal dominant"				
chr3	94057921	94063388	3q11.2	3q11.2		616588	DHFRL1	Dihydrofolate reductase-like 1	DHFR2	200895	ENSG00000178700						
chr3	94062904	94131831	3q11.2	3q11.2		617491	NSUN3	"NOP2/SUN RNA methyltransferase family, member 3"	NSUN3	63899	ENSG00000178694			Nsun3 (MGI:2146565)			
chr3	96814580	97761531	3q11.2	3q11.2		600066	"EPHA6, HEK12, EHK2"	Ephrin receptor EphA6	EPHA6	285220	ENSG00000080224			Epha6 (MGI:108034)			
chr3	97762580	97812584	3p12-q13	3q11.2		608845	"ARL6, BBS3, RP55"	ADP-ribosylation factor-like 6	ARL6	84100	ENSG00000113966	mutation identified in 1 RPS55 family	"{Bardet-Biedl syndrome 1, modifier of}, 209900 (3), Autosomal recessive, Digenic recessive; Bardet-Biedl syndrome 3, 600151 (3), Autosomal recessive; ?Retinitis pigmentosa 55, 613575 (3)"	Arl6 (MGI:1927136)			
chr3	97941816	97972450	3q12.1	3q11.2		612049	"MINA, MINA53, MDIG"	MYC-induced nuclear antigen	RIOX2	84864	ENSG00000170854			Riox2 (MGI:1914264)			
chr3	98531898	98534678	3q11.2-q13.1	3q11.2		601166	GPR15	G protein-coupled receptor-15	GPR15	2838	ENSG00000154165			Gpr15 (MGI:1918473)			
chr3	98569836	98593683	3q12	3q11.2		612732	CPOX	Coproporphyrinogen oxidase	CPOX	1371	ENSG00000080819		"Coproporphyria, 121300 (3), Autosomal dominant; Harderoporphyria, 121300 (3), Autosomal dominant"	Cpox (MGI:104841)			
chr3	98732235	98795844	3q12.1	3q12.1		607156	"ST3GAL6, ST3GALVI"	"ST3 beta-galactoside alpha-2,3-sialyltransferase 6"	ST3GAL6	10402	ENSG00000064225			St3gal6 (MGI:1888707)			
chr3	98795969	98901691	3q12.1	3q12.1		608698	"DCBLD2, ESDN"	"Discoidin, CUB, and LCCL domain-containing protein 2"	DCBLD2	131566	ENSG00000057019			Dcbld2 (MGI:1920629)			
chr3	99638595	99796732	3q12-q13.1	3q12.1		120251	COL8A1	"Collagen VIII, alpha-1 polypeptide"	COL8A1	1295	ENSG00000144810			Col8a1 (MGI:88463)			
chr3	99833143	100114512	3q12.1	3q12.1		612993	FILIP1L	Filamin A-interacting protein 1-like	FILIP1L	11259	ENSG00000168386			Filip1l (MGI:1925999)			
chr3	100185823	100194185	3q12	3q12.1		611030	"TMEM30C, CDC50C"	Transmembrane protein 30C	TMEM30CP	644444							
chr3	100260816	100325251	3q12.1-q12.2	3q12.1-q12.2		617687	"TBC1D23, PCH11"	"TBC1 domain family, member 23"	TBC1D23	55773	ENSG00000036054		"Pontocerebellar hypoplasia, type 11, 617695 (3), Autosomal recessive"	Tbc1d23 (MGI:1914831)			
chr3	100334717	100355633	3q12.2	3q12.2		616769	NIT2	Nitrilase family member 2	NIT2	56954	ENSG00000114021			Nit2 (MGI:1261838)			
chr3	100363458	100401397	3q12.2	3q12.2		606081	TOMM70A	"Translocase of outer mitochondrial membrane 70, yeast, homolog of, A"	TOMM70	9868	ENSG00000154174			Tomm70a (MGI:106295)			
chr3	100492618	100577452	3q12.2	3q12.2		616928	"TMEM45A, DERP7, DNAPTP4"	Transmembrane protein 45A	TMEM45A	55076	ENSG00000181458			Tmem45a (MGI:1913122)			
chr3	100609588	100696173	3q12.2	3q12.2		612307	"ADGRG7, GPR128"	Adhesion G protein-coupled receptor G7	ADGRG7	84873	ENSG00000144820			Adgrg7 (MGI:2441732)			
chr3	100709289	100748966	3q11-q12	3q12.2		602498	"TFG, HMSNP, SPG57"	TRK-fused gene	TFG	10342	ENSG00000114354	fused with NR4A3 or NTRK1; mutation identified in 1 SPG57 family	"Hereditary motor and sensory neuropathy, Okinawa type, 604484 (3), Autosomal dominant; ?Spastic paraplegia 57, autosomal recessive, 615658 (3), Autosomal recessive"	Tfg (MGI:1338041)			
chr3	100749328	100993507	3q12	3q12.2		606279	TARSH	Target of Nesh-SH3	ABI3BP	25890	ENSG00000154175						
chr3	101222545	101320574	3q11.2	3q12.3		607056	"IMPG2, IPM200, RP56, VMD5"	Interphotoreceptor matrix proteoglycan 2	IMPG2	50939	ENSG00000081148		"Macular dystrophy, vitelliform, 5, 616152 (3), Autosomal dominant; Retinitis pigmentosa 56, 613581 (3), Autosomal recessive"	Impg2 (MGI:3044955)			
chr3	101324188	101513882	3q12.3	3q12.3		612846	"SENP7, KIAA1707"	"Sentrin-specific protease family, member 7"	SENP7	57337	ENSG00000138468			Senp7 (MGI:1913565)			
chr3	101561835	101566445	3q12.3	3q12.3		615423	"TRMT10C, RG9MTD1, MRPP1, COXPD30"	"tRNA methyltransferase 10, S. cerevisiae, homolog of, C"	TRMT10C	54931	ENSG00000174173		"Combined oxidative phosphorylation deficiency 30, 616974 (3), Autosomal recessive"	Trmt10c (MGI:1196261)			
chr3	101574093	101594464	3q12.3	3q12.3		615210	PCNP	PEST-containing nuclear protein	PCNP	57092	ENSG00000081154			Pcnp (MGI:1923552)			
chr3	101681089	101686718	3q	3q12.3		604180	RPL24	Ribosomal protein L24	RPL24	6152	ENSG00000114391			Rpl24 (MGI:1915443)			
chr3	101723930	101770561	3q12.2	3q12.3		615864	CEP97	"Centrosomal protein, 97kD"	CEP97	79598	ENSG00000182504			Cep97 (MGI:1921451)			
chr3	101827989	101861024	3q13.11	3q12.3		608004	"NFKBIZ, INAP, MAIL, IKBZ"	"Nuclear factor of kappa light chain gene enhancer in B cells inhibitor, zeta"	NFKBIZ	64332	ENSG00000144802			Nfkbiz (MGI:1931595)			
chr3	102385143	102479840	3q12.3	3q12.3		615915	ZPLD1	Zona pellucida-like domain-containing protein 1	ZPLD1	131368	ENSG00000170044			Zpld1 (MGI:2443415)			
chr3	103100000	111600000	3q13.1			600467	MHS4	Malignant hyperthermia susceptibility 4	MHS4	4265			"{Malignant hyperthermia susceptibility 4}, 600467 (2), Autosomal dominant"				
chr3	105366712	105576912	3q13.1-q13.2	3q13.11		601662	ALCAM	Activated leukocyte cell adhesion molecule	ALCAM	214	ENSG00000170017			Alcam (MGI:1313266)			
chr3	105655460	105869551	3q13.11	3q13.11		604491	CBLB	CAS-BR-M murine ecotropic retroviral transforming sequence B	CBLB	868	ENSG00000114423			Cblb (MGI:2146430)			
chr3	107240691	107326963	3q13.12	3q13.12		616619	"DUBR, DUM, LINC0883"	"DPPA2 upstream-binding RNA, noncoding"	DUBR	344595							
chr3	108043093	108094199	3q13.1-q13.2	3q13.12		601028	"CD47, MER6, IAP"	CD47 antigen (Rh-related antigen; integrin-associated protein)	CD47	961	ENSG00000196776			Cd47 (MGI:96617)			
chr3	108160811	108222569	3p12-q13	3q13.12-q13.13		606621	"IFT57, ESRRBL1, HIPPI, OFD18"	"Intraflagellar transport 57, chlamydomonas, homolog of (HIP1 protein interactor)"	IFT57	55081	ENSG00000114446	mutation identified in 1 OFD18 family	"?Orofaciodigital syndrome XVIII, 617927 (3)"	Ift57 (MGI:1921166)			
chr3	108296489	108378284	3q13.13	3q13.13		604371	HHLA2	Human endogenous retrovirus-H long terminal repeat-associating 2	HHLA2	11148	ENSG00000114455						
chr3	108380368	108549461	3q13.13	3q13.13		609929	MYH15	"Myosin, heavy chain 15"	MYH15	22989	ENSG00000144821			Myh15 (MGI:3643515)			
chr3	108545751	108589643	3q13.13	3q13.13		610643	"KIAA1524, p90"	KIAA1524 gene	CIP2A	57650	ENSG00000163507			C330027C09Rik (MGI:2146335)			
chr3	108589489	108694845	3q13.13	3q13.13		608672	"DZIP3, KIAA0675"	DAZ-interacting zinc finger protein 3	DZIP3	9666	ENSG00000198919			Dzip3 (MGI:1917433)			
chr3	108755638	108757282	3q13.13	3q13.13		605645	"RETNLB, RELMB, FIZZ2"	"Resistin-like protein, beta"	RETNLB	84666	ENSG00000163515			Retnlb (MGI:1888505)			
chr3	108822697	108855004	3q13	3q13.13		604962	"TRAT1, TRIM"	T-cell receptor-associated transmembrane adaptor 1	TRAT1	50852	ENSG00000163519			Trat1 (MGI:1924897)			
chr3	108907643	108955194	3q13.1	3q13.13		605128	"GUCA1C, GCAP3"	Guanylate cyclase activator 1C	GUCA1C	9626	ENSG00000138472						
chr3	108958238	109118145	3q13	3q13.13		603205	MORC1	"MORC family CW-type zinc finger 1 (microrchidia, mouse, homolog of)"	MORC1	27136	ENSG00000114487			Morc1 (MGI:1316740)			
chr3	109293787	109316588	3q13.13	3q13.13		614445	"DPPA2, PESCRG1, ECAT15-2"	Developmental pluripotency-associated gene 2	DPPA2	151871	ENSG00000163530			Dppa2 (MGI:2157523)			
chr3	109326140	109339634	3q13.13	3q13.13		614125	DPPA4	Developmental pluripotency-associated gene 4	DPPA4	55211	ENSG00000121570			Dppa4 (MGI:2157525)			
chr3	111071758	111201443	3q13	3q13.13		607147	"NECTIN3, PVRL3, PRR3"	Nectin 3	NECTIN3	25945	ENSG00000177707			Nectin3 (MGI:1930171)			
chr3	111542078	111665995	3q13.13	3q13.1-q13.2		606037	"CD96, TACTILE"	CD96 antigen	CD96	10225	ENSG00000153283		"C syndrome, 211750 (3), Autosomal dominant"	Cd96 (MGI:1934368)			
chr3	111592899	111595334	3q13.2	3q13.13		615246	ZBED2	Zinc finger BED domain-containing protein 2	ZBED2	79413	ENSG00000177494						
chr3	111600000	122200000	3q13.2-q13.33			614655	STUT3	"Stuttering, familial persistent, 3"		100909386		max lod at D3S1310	"Stuttering, familial persistent, 3, 614655 (2)"				
chr3	111674675	111846446	3q13.2	3q13.2		617015	PLCXD1	"Phospholipase C, phosphatidylinositol-specific, X domain-containing protein 2"	PLCXD2	257068	ENSG00000240891			Plcxd2 (MGI:3647874)			
chr3	111732479	111976516	3q13.2	3q13.2		610298	PHLDB2	"Pleckstrin homology-like domain, family B, member 2"	PHLDB2	90102	ENSG00000144824			Phldb2 (MGI:2444981)			
chr3	111998738	112013887	3q13.2	3q13.2		607953	"TAGLN3, NP24, NP22"	Transgelin 3	TAGLN3	29114	ENSG00000144834			Tagln3 (MGI:1926784)			
chr3	112086334	112136378	3q13.2	3q13.2		611956	"C3orf52, TTMP"	Chromosome 3 open reading frame 52	C3orf52	79669	ENSG00000114529			BC016579 (MGI:2384848)			
chr3	112120840	112133955	3q13	3q13.2		607792	"GCET2, HGAL"	Germinal center-expressed transcript 2	GCSAM	257144	ENSG00000174500			Gcsam (MGI:102969)			
chr3	112140897	112294257	3q13.2	3q13.2		612738	SLC9A10	"Solute carrier family 9, member 10"	SLC9C1	285335	ENSG00000172139			Slc9c1 (MGI:2685456)			
chr3	112332223	112362811	3q12-q13	3q13.2		155970	MOX2	MRC OX-2 antigen	CD200	4345	ENSG00000091972			Cd200 (MGI:1196990)			
chr3	112463029	112499756	3q13.2	3q13.2		607925	BTLA	B- and T-lymphocyte attenuator	BTLA	151888	ENSG00000186265			Btla (MGI:2658978)			
chr3	112604385	112641142	3q13.2	3q13.2		608298	"URB, SSG1"	"Urb, mouse, homolog of"	CCDC80	151887	ENSG00000091986			Ccdc80 (MGI:1915146)			
chr3	112922684	112975089	3q13.1	3q13.2		607546	"CD200R1, MOX2R, OX2R"	CD200 receptor 1	CD200R1	131450	ENSG00000163606			Cd200r1 (MGI:1889024)			
chr3	113002443	113019732	3q13.2	3q13.2		617089	"NEPRO, C3orf17"	Nucleolus and neural progenitor protein	NEPRO	25871	ENSG00000163608			Nepro (MGI:2384836)			
chr3	113286929	113441513	3q13.2	3q13.2		617559	"CFAP44, WDR52, SPGF20"	Cilia- and flagella-associated protein 44	CFAP44	55779	ENSG00000206530	mutation identified in 1 SPGF20 patient	"?Spermatogenic failure 20, 617593 (3), Autosomal recessive"	Cfap44 (MGI:1277238)			
chr3	113442717	113515186	3q13.2	3q13.2		613447	"SPICE1, CCDC52"	Spindle- and centriole-associated protein 1	SPICE1	152185	ENSG00000163611			Spice1 (MGI:1196252)			
chr3	113648384	113696656	3q13.2	3q13.2		617568	USF3	"Upstream transcription factor family, member 3"	USF3	205717	ENSG00000176542			Usf3 (MGI:2685454)			
chr3	113700000	117600000	3q13.31			615433	"DEL3q13.31, C13DELq13.31"	Chromosome 3q13.31 deletion syndrome					"Chromosome 3q13.31 deletion syndrome, 615433 (4), Autosomal dominant"				
chr3	113716459	113746298	3q13.2	3q13.31		610834	"NAT13, NAT5, SAN"	N-acetyltransferase 13	NAA50	80218	ENSG00000121579			Naa50 (MGI:1919367)			
chr3	113747018	113812057	3p13	3q13.31		607027	"ATP6V1A1, HO68, ARCL2D"	"ATPase, H+ transporting, lysosomal alpha polypeptide, 70-kD, isoform 1"	ATP6V1A	523	ENSG00000114573		"Cutis laxa, autosomal recessive, type IID, 617403 (3), Autosomal recessive"	Atp6v1a (MGI:1201780)			
chr3	113947900	113998001	3q13.31	3q13.31		617334	"ZDHHC23, NIDD"	Zinc finger DHHC-type containing 23	ZDHHC23	254887	ENSG00000184307			Zdhhc23 (MGI:2685625)			
chr3	114127622	114199406	3q13.3	3q13.31		126451	"DRD3, ETM1, FET1"	Dopamine receptor D3	DRD3	1814	ENSG00000151577		"{Essential tremor, hereditary, 1}, 190300 (3), Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"	Drd3 (MGI:94925)			
chr3	114234630	114237577	3p12-qter	3q13.31		194553	ZNF80	Zinc finger protein-80 (pT17)	ZNF80	7634	ENSG00000174255						
chr3	114291101	114329746	3q13.3	3q13.31		612859	TIGIT	T-cell immunoreceptor with immunoglobulin and ITIM domains	TIGIT	201633	ENSG00000181847			Tigit (MGI:3642260)			
chr3	114314499	115147279	3q13.2	3q13.31		606025	"ZBTB20, ZNF288, DPZF, PRIMS"	Zinc finger and BTB-domain containing 20	ZBTB20	26137	ENSG00000181722		"Primrose syndrome, 259050 (3), Autosomal dominant"	Zbtb20 (MGI:1929213)			
chr3	115623303	115721486	3q13	3q13.31		162060	GAP43	Neuron growth-associated protein 43	GAP43	2596	ENSG00000172020			Gap43 (MGI:95639)			
chr3	115802362	116445537	3q13.2-q21	3q13.31		603241	"LSAMP, LAMP"	Limbic system-associated membrane protein	LSAMP	4045	ENSG00000185565			Lsamp (MGI:1261760)			
chr3	116709787	116717039	3q13.31	3q13.31		616057	"TUSC7, LSAMPAS3, LOC285194"	"Tumor suppressor candidate 7, noncoding"	TUSC7	285194							
chr3	119173577	119205152	3q13.3-q21	3q13.32		602380	UPK1B	Uroplakin 1B	UPK1B	7348	ENSG00000114638			Upk1b (MGI:98912)			
chr3	119211741	119240906	3q13.3	3q13.32		604015	B4GALT4	"Beta-1,4-galactosyltransferase 4"	B4GALT4	8702	ENSG00000121578			B4galt4 (MGI:1928387)			
chr3	119294288	119419475	3q13.3	3q13.32-q13.33		610911	"ARHGAP31, CDGAP, KIAA1204, AOS1"	Rho GTPase-activating protein 31	ARHGAP31	57514	ENSG00000031081		"Adams-Oliver syndrome 1, 100300 (3), Autosomal dominant"	Arhgap31 (MGI:1333857)			
chr3	119468937	119494707	3q13.33	3q13.33		615618	"POGLUT1, CLP46, KTELC1, RUMI, C3orf9, DDD4, LGMD2Z"	Protein O-glucosyltransferase 1	POGLUT1	56983	ENSG00000163389	mutation identified in 1 LGMD2Z family	"Dowling-Degos disease 4, 615696 (3), Autosomal dominant; ?Muscular dystrophy, limb-girdle, type 2Z, 617232 (3), Autosomal recessive"	Poglut1 (MGI:2444232)			
chr3	119498520	119524280	3q13.33	3q13.33		615534	"TIMMDC1, C3orf1"	Translocase of inner mitochondrial membrane domain-containing protein 1	TIMMDC1	51300	ENSG00000113845		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Timmdc1 (MGI:1922139)			
chr3	119523908	119559633	3q21	3q13.33		112203	"CD80, CD28LG, LAB7"	"CD80 antigen (CD28 antigen ligand 1, B7-1 antigen)"	CD80	941	ENSG00000121594			Cd80 (MGI:101775)			
chr3	119579432	119589953	3q13.33	3q13.33		603081	ADPRH	ADP-ribosylarginine hydrolase	ADPRH	141	ENSG00000144843			Adprh (MGI:1098234)			
chr3	119597847	119629810	3q13.2-q13.3	3q13.33		607460	"PLA1A, PSPLA1"	Phosphatidylserine-specific phospholipase A1-alpha	PLA1A	51365	ENSG00000144837			Pla1a (MGI:1934677)			
chr3	119642051	119660589	3q13.3	3q13.33		605823	"POPDC2, POP2"	Popeye domain-containing protein 2	POPDC2	64091	ENSG00000121577			Popdc2 (MGI:1930150)			
chr3	119669524	119677395	3q	3q13.33		604813	COX17	Cytochrome c oxidase assembly protein COX17	COX17	10063	ENSG00000138495	pseudogene on chr. 13?		Cox17 (MGI:1333806)			
chr3	119703021	119767101	3q13.3-q21.1	3q13.33		609910	"MAATS1, AAT1, C3orf15"	MYCBP-associated testis-expressed protein 1	MAATS1	89876	ENSG00000183833			Maats1 (MGI:2443598)			
chr3	119780483	119818484	3q13-q21	3q13.33		603065	"NR1I2, PXR, SXR, PARq"	"Nuclear receptor subfamily 1, group I, member 2"	NR1I2	8856	ENSG00000144852			Nr1i2 (MGI:1337040)			
chr3	119821320	120095822	3q13.3	3q13.33		605004	GSK3B	Glycogen synthase kinase 3-beta	GSK3B	2932	ENSG00000082701			Gsk3b (MGI:1861437)			
chr3	120165480	120285073	3q13.33	3q13.33		610464	"GPR156, GABABL"	G protein-coupled receptor 156	GPR156	165829	ENSG00000175697			Gpr156 (MGI:2653880)			
chr3	120394213	120451070	3q13.3	3q13.33		605547	"FSTL1, FRP, MIR198"	Follistatin-like 1	FSTL1	11167	ENSG00000163430	FSTL1 mRNA can encode a protein or produce an micoRNA		Fstl1 (MGI:102793)			
chr3	120596280	120602410	3q13.33	3q13.33		603840	NDUFB4	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 4"	NDUFB4	4710	ENSG00000065518			"Gm3244,Gm3873,Ndufb4 (MGI:3781422,MGI:3782046,MGI:1915444)"			
chr3	120628167	120682570	3q13.33	3q13.33		607474	"HGD, AKU"	"Homogentisate 1,2-dioxygenase (homogentisate oxidase)"	HGD	3081	ENSG00000113924		"Alkaptonuria, 203500 (3), Autosomal recessive"	Hgd (MGI:96078)			
chr3	120742710	120783133	3q13.33	3q13.33		189962	"GTF2E1, TF2E1"	"General transcription factor IIE, polypeptide 1"	GTF2E1	2960	ENSG00000153767			Gtf2e1 (MGI:1921447)			
chr3	120908202	121424760	3q13.3	3q13.33		609381	"STXBP5L, LLGL4"	Syntaxin-binding protein 5-like	STXBP5L	9515	ENSG00000145087			Stxbp5l (MGI:2443815)			
chr3	121431419	121546005	3q13.3	3q13.33		604419	POLQ	"Polymerase, DNA, theta"	POLQ	10721	ENSG00000051341			Polq (MGI:2155399)			
chr3	121567930	121590621	3q13.3	3q13.33		611164	ARGFX	Arginine-fifty homeobox	ARGFX	503582	ENSG00000186103	pseudogenes on 5q23.2 and 17q11.2					
chr3	121593322	121630291	3q21.1	3q13.33		609107	"FBXO40, FBX40, KIAA1195"	F-box only protein 40	FBXO40	51725	ENSG00000163833			Fbxo40 (MGI:2443753)			
chr3	121631397	121660947	3q13	3q13.33		601306	HCLS1	Hematopoietic cell-specific Lyn substrate 1	HCLS1	3059	ENSG00000180353			Hcls1 (MGI:104568)			
chr3	121663198	121751168	3q13	3q13.33		602500	"GOLGB1, GCP372"	"Golgi autoantigen, golgin subfamily B, 1"	GOLGB1	2804	ENSG00000173230			Golgb1 (MGI:1099447)			
chr3	121769760	121835078	3q13.33	3q13.33		609237	"IQCB1, NPHP5, KIAA0036"	IQ motif-containing protein B1	IQCB1	9657	ENSG00000173226		"Senior-Loken syndrome 5, 609254 (3), Autosomal recessive"	Iqcb1 (MGI:2443764)			
chr3	121835179	121886525	3q13.33	3q13.33		607659	EAF2	ELL-associated factor 2	EAF2	55840	ENSG00000145088			Eaf2 (MGI:2146616)			
chr3	121894323	121944186	3q13.33	3q13.33		602339	"SLC15A2, PEPT2"	"Solute carrier family 15 (H+/peptide transporter), member 2"	SLC15A2	6565	ENSG00000163406			Slc15a2 (MGI:1890457)			
chr3	121987322	122060553	3q21.1	3q13.33		609739	"ILDR1, DFNB42"	Immunoglobulin-like domain-containing receptor 1	ILDR1	286676	ENSG00000145103		"Deafness, autosomal recessive 42, 609646 (3), Autosomal recessive"	Ildr1 (MGI:2146574)			
chr3	122055361	122121142	3q21	3q13.33		601020	"CD86, CD28LG2, LAB72"	"CD86 antigen (CD28 antigen ligand 2, B7-2 antigen)"	CD86	942	ENSG00000114013			Cd86 (MGI:101773)			
chr3	122183682	122286502	3q21.1	3q13.3-q21.1		601199	"CASR, HHC1, PCAR1, FIH, EIG8, HYPOC1"	Calcium-sensing receptor	CASR	846	ENSG00000036828	15cM from RHO	"{Calcium, serum level of} (3); {Epilepsy idiopathic generalized, susceptibility to, 8}, 612899 (3); Hypercalciuric hypercalcemia (3); Hyperparathyroidism, neonatal, 239200 (3), Autosomal recessive, Autosomal dominant; Hypocalcemia, autosomal dominant, 601198 (3), Autosomal dominant; Hypocalcemia, autosomal dominant, with Bartter syndrome, 601198 (3), Autosomal dominant; Hypocalciuric hypercalcemia, type I, 145980 (3), Autosomal dominant"	Casr (MGI:1351351)			
chr3	122200000	129500000	3q21			603165	ATOD1	"Dermatitis, atopic, 1"		64069		max lod at D3S3606	"{Dermatitis, atopic, susceptibility to, 1}, 603165 (2), Autosomal dominant"				
chr3	122200000	155300000	3q21-q25.2			614011	"ERVK-4, HERV-KI"	"Endogenous retrovirus group K, member 4"	ERVK-4	60359							
chr3	122200000	129500000	3q21			613460	"FGQTL6, BWQTL3, PGQTL1"	"Fasting plasma glucose level QTL 6; Birth weight QTL 3; Plasma glucose, 2-hour, QTL 1"		100499168		associated with rs11708067 and rs11708067	"[Birth weight QTL 3], 613460 (2); [Fasting plasma glucose level QTL 6], 613460 (2); [Plasma glucose, 2-hour, QTL 1], 613460 (2)"				
chr3	122200000	149200000	3q21-q24			601682	GLC1C	"Glaucoma 1, open angle, C"	GLC1C	2723			"Glaucoma 1C, primary open angle, 601682 (2), Autosomal dominant"				
chr3	122200000	139000000	3q21-q22			601471	"HCFP1, MBS2"	"Facial paresis, hereditary congenital, 1"	MBS2	7880			"Facial paresis, hereditary congenital, 1, 601471 (2), Autosomal dominant"				
chr3	122200000	129500000	3q21			604316	PSORS5	Psoriasis susceptibility 5	PSORS5	63870			"{Psoriasis susceptibility 5}, 604316 (2)"				
chr3	122325163	122341968	3q21	3q21.1		184600	"CSTA, STFA, STF1, AREI, PSS4"	Cystatin A (stefin A)	CSTA	1475	ENSG00000121552		"Peeling skin syndrome 4, 607936 (3), Autosomal recessive"	"Gm5483,2010005H15Rik,Csta1 (MGI:3524930,MGI:1924020,MGI:3645124)"			
chr3	122384175	122410113	3q21.1	3q21.1		608017	"C3orf28, E2IG5"	E2-induced gene 5	FAM162A	26355	ENSG00000114023			Fam162a (MGI:1917436)			
chr3	122421900	122514938	3q21	3q21.1		600686	"KPNA1, RCH2, SRP1"	"Karyopherin, alpha-1"	KPNA1	3836	ENSG00000114030			Kpna1 (MGI:103560)			
chr3	122527909	122564675	3q21	3q21.1		612065	"PARP9, BAL1, BAL"	Poly(ADP-ribose) polymerase 9	PARP9	83666	ENSG00000138496			Parp9 (MGI:1933117)			
chr3	122564337	122575202	3q21	3q21.1		613143	"DTX3L, BBAP"	DTX3-like	DTX3L	151636	ENSG00000163840	head-to-head with PARP9		Dtx3l (MGI:2656973)			
chr3	122575925	122639046	3q21	3q21.1		612066	"PARP15, BAL3"	Poly(ADP-ribose) polymerase 15	PARP15	165631	ENSG00000173200						
chr3	122680725	122730839	3q21.1	3q21.1		610028	"PARP14, KIAA1268"	Poly(ADP-ribose) polymerase 14	PARP14	54625	ENSG00000173193			Parp14 (MGI:1919489)			
chr3	122795053	122892156	3q21	3q21.1		602773	"DIRC2, RCC4"	Disrupted in renal carcinoma 2	DIRC2	84925	ENSG00000138463	t(2;3)(q35;q21) in renal cell carcinoma	"Renal cell carcinoma, 144700 (1)"	Dirc2 (MGI:2387188)			
chr3	123067008	123162105	3q21.1	3q21.1		616942	"PDIA5, PDIR"	"Protein disulfide isomerase, family A, member 5"	PDIA5	10954	ENSG00000065485			Pdia5 (MGI:1919849)			
chr3	123201926	123274135	3q21.1	3q21.1		612442	"SEC22A, SEC22L2"	"Secretion deficient 22, S. cerevisiae, homolog of, A"	SEC22A	26984	ENSG00000121542			Sec22a (MGI:2447876)			
chr3	123282295	123448987	3q13.2-q21	3q21.1		600293	"ADCY5, FDFM"	Adenylate cyclase-5	ADCY5	111	ENSG00000173175		"Dyskinesia, familial, with facial myokymia, 606703 (3), Autosomal dominant"	Adcy5 (MGI:99673)			
chr3	123491547	123585184	3q21.1	3q21.1		615939	"PTPLB, HACD2"	"Protein tyrosine phosphatase-like (proline instead of catalytic arginine), member B"	HACD2	201562	ENSG00000206527			Hacd2 (MGI:1918007)			
chr3	123612295	123884301	3q21	3q21.1		600922	"MYLK, MLCK, AAT7"	Myosin-light-polypeptide kinase	MYLK	4638	ENSG00000065534	pseudogene on 3p13	"Aortic aneurysm, familial thoracic 7, 613780 (3), Autosomal dominant"	Mylk (MGI:894806)			
chr3	123887382	123961411	3q21.1	3q21.1		617147	CCDC14	Coiled-coil domain-containing protein 14	CCDC14	64770	ENSG00000175455			Ccdc14 (MGI:2443448)			
chr3	123969005	123992169	3q21.1	3q21.1		611757	"ROPN1, ODF6"	Rhophilin-associated tail protein 1	ROPN1	54763	ENSG00000065371			Ropn1 (MGI:1923628)			
chr3	124033340	124726324	3q13	3q21.1-q21.2		604605	"KALRN, HAPIP, DUO, CHDS5"	Kalirin	KALRN	8997	ENSG00000160145		"{Coronary heart disease, susceptibility to, 5}, 608901 (3)"	Kalrn (MGI:2685385)			
chr3	124730365	124749272	3q13	3q21.2		613891	"UMPS, OPRT"	Uridine monophosphate synthetase (orotate phosphoribosyl transferase and orotidine-5'-decarboxylase)	UMPS	7372	ENSG00000114491		"Orotic aciduria, 258900 (3), Autosomal recessive"	Umps (MGI:1298388)			
chr3	124761947	124901410	3q21.2	3q21.2		147561	ITGB5	"Integrin, beta-5"	ITGB5	3693	ENSG00000082781			Itgb5 (MGI:96614)			
chr3	124905441	124934750	3q13.3	3q21.2		612181	MUC13	"Mucin 13, cell surface-associated"	MUC13	56667	ENSG00000173702			Muc13 (MGI:103190)			
chr3	124965709	125055957	3q21.2	3q21.2		614182	"HEG1, KIAA1237"	"Heart of glass, zebrafish, homolog of, 1"	HEG1	57493	ENSG00000173706			Heg1 (MGI:1924696)			
chr3	125225668	125375353	3q21	3q21.2		601897	"ZNF148, ZFP148, GDACCF"	Zinc finger protein-148	ZNF148	7707	ENSG00000163848		"Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies, 617260 (3), Autosomal dominant"	Zfp148 (MGI:1332234)			
chr3	125446643	125520213	3q21.2	3q21.2		605931	SNX4	Sorting nexin 4	SNX4	8723	ENSG00000114520			Snx4 (MGI:1916400)			
chr3	125528857	125595536	3q21.1	3q21.2		606739	"OSBPL11, ORP11"	Oxysterol-binding protein-like protein 11	OSBPL11	114885	ENSG00000144909	previously assigned to chr.8		Osbpl11 (MGI:2146553)			
chr3	126006356	126101549	3q21.2	3q21.2-q21.3		610803	SLC41A3	"Solute carrier family 41, member 3"	SLC41A3	54946	ENSG00000114544			Slc41a3 (MGI:1918949)			
chr3	126103560	126197757	3q21.3	3q21.3		600249	"ALDH1L1, FTHFD"	"Aldehyde dehydrogenase 1 family, member L1"	ALDH1L1	10840	ENSG00000144908			Aldh1l1 (MGI:1340024)			
chr3	126288120	126357392	3q21-q22	3q21.3		606465	"KLF15, KKLF"	Kruppel-like factor 15	KLF15	28999	ENSG00000163884			Klf15 (MGI:1929988)			
chr3	126437347	126475937	3q21.3	3q21.3		615746	ZXDC	ZCD family zinc finger protein C	ZXDC	79364	ENSG00000070476			Zxdc (MGI:1933108)			
chr3	126481164	126517772	3q21.3	3q21.3		613012	"UROC1, UROCD"	Urocanase domain-containing protein 1	UROC1	131669	ENSG00000159650	mutation identified in 1 UROCD patient	"?Urocanase deficiency, 276880 (3), Autosomal recessive"	Uroc1 (MGI:2385332)			
chr3	126524287	126543290	3p21.3	3q21.3		610124	"CHST13, C4ST3"	Carbohydrate sulfotransferase 13	CHST13	166012	ENSG00000180767			Chst13 (MGI:1919047)			
chr3	126607051	126655123	3q21	3q21.3		606235	"TXNRD3, TRXR3, TR2"	Thioredoxin reductase 3	TXNRD3	114112	ENSG00000197763			Txnrd3 (MGI:2386711)			
chr3	126704219	126960419	3q21.3	3q21.3		615634	"CHCHD6, CHCM1"	Coiled-coil-helix-coiled-coil-helix domain-containing protein 6	CHCHD6	84303	ENSG00000159685			Chchd6 (MGI:1913348)			
chr3	126983258	127037391	3q21-qter	3q21.3		601055	"PLXNA1, NOVP, NOV, PLXN1"	Plexin A1 (NOV transmembrane protein)	PLXNA1	5361	ENSG00000114554			Plxna1 (MGI:107685)			
chr3	127598356	127622435	3q21	3q21.3		116945	"MCM2, CDCL1, DFNA70"	"Minichromosome maintenance deficient, S. cerevisiae, 2, homolog of (mitotin)"	MCM2	4171	ENSG00000073111	mutation identified in 1 DFNA70 family	"?Deafness, autosomal dominant 70, 616968 (3), Autosomal dominant"	Mcm2 (MGI:105380)			
chr3	127629158	127672809	3q21.3	3q21.3		616627	"PODXL2, EG"	Podocalyxin-like 2	PODXL2	50512	ENSG00000114631			Podxl2 (MGI:2442488)			
chr3	127672927	127680925	3q21	3q21.3		608308	"ABTB1, BPOZ"	Ankyrin repeat and BTB/POZ domain containing 1	ABTB1	80325	ENSG00000114626			Abtb1 (MGI:1933148)			
chr3	127689061	127823249	3p21.3	3q21.3		609699	"MGLL, MGL, HUK5"	Monoglyceride lipase	MGLL	11343	ENSG00000074416			Mgll (MGI:1346042)			
chr3	128052368	128071682	3q21.3	3q21.3		609213	"SEC61A1, SEC61, HNFJ4"	"Sec61 complex, alpha-1 subunit"	SEC61A1	29927	ENSG00000058262		"Hyperuricemic nephropathy, familial juvenile, 4, 617056 (3), Autosomal dominant"	Sec61a1 (MGI:1858417)			
chr3	128064610	128153913	3q21	3q21.3		603449	"RUVBL1, NMP238, TIP49"	"RUVB, E. coli, homolog-like 1"	RUVBL1	8607	ENSG00000175792			Ruvbl1 (MGI:1928760)			
chr3	128153452	128426192	3q21.3	3q21.3		607695	"EEFSEC, SELB, EFSEC"	"Eukaryotic elongation factor, selenocysteine-tRNA-specific"	EEFSEC	60678	ENSG00000132394			Eefsec (MGI:2137092)			
chr3	128462431	128467247	3q21.3	3q21.3		611337	"DNAJB8, DJ6"	"DNAJ/HSP40 homolog, subfamily B, member 8"	DNAJB8	165721	ENSG00000179407			Dnajb8 (MGI:1922801)			
chr3	128479421	128493186	3q21	3q21.3		137295	"GATA2, DCML, MONOMAC, IMD21"	GATA-binding protein-2	GATA2	2624	ENSG00000179348		"Emberger syndrome, 614038 (3), Autosomal dominant; Immunodeficiency 21, 614172 (3), Autosomal dominant; {Leukemia, acute myeloid, susceptibility to}, 601626 (3), Autosomal dominant; {Myelodysplastic syndrome, susceptibility to}, 614286 (3)"	Gata2 (MGI:95662)			
chr3	128619969	128650875	3q	3q21.3		180470	RPN1	Ribophorin I	RPN1	6184	ENSG00000163902			Rpn1 (MGI:98084)			
chr3	128726135	128814797	3q21	3q21.3		602298	"RAB7, CMT2B, PSN"	Ras-associated protein RAB7	RAB7A	7879	ENSG00000075785		"Charcot-Marie-Tooth disease, type 2B, 600882 (3), Autosomal dominant"	Rab7 (MGI:105068)			
chr3	128879489	128913113	3q26	3q21.3		611103	ACAD9	"Acyl-CoA dehydrogenase family, member 9"	ACAD9	28976	ENSG00000177646		"Mitochondrial complex I deficiency due to ACAD9 deficiency, 611126 (3), Autosomal recessive"	Acad9 (MGI:1914272)			
chr3	129055448	129062410	3q21	3q21.3		173515	GP9	"Glycoprotein IX, platelet"	GP9	2815	ENSG00000169704		"Bernard-Soulier syndrome, type C, 231200 (3), Autosomal recessive"	Gp9 (MGI:1860137)			
chr3	129127415	129161229	3q21.3	3q21.3		612764	"ISY1, KIAA1160"	"ISY1 splicing factor, S. cerevisiae, homolog of"	ISY1	57461	ENSG00000240682						
chr3	129167814	129183966	3q13.3-q24	3q21.3		116955	"ZNF9, CNBP1, DM2, PROMM"	Zinc finger protein-9 (a cellular retroviral nucleic acid-binding protein)	CNBP	7555	ENSG00000169714		"Myotonic dystrophy 2, 602668 (3), Autosomal dominant"	Cnbp (MGI:88431)			
chr3	129249574	129277772	3q21.3	3q21.3		615525	COPG1	"Coatomer protein complex, subunit gamma-1"	COPG1	22820	ENSG00000181789			Copg1 (MGI:1858696)			
chr3	129314770	129316276	3q21.3	3q21.3		602785	"H1FX, H1X"	"H1 histone family, member X"	H1FX	8971	ENSG00000184897			H1fx (MGI:2685307)			
chr3	129430943	129440178	3q21-q22	3q21.3		603574	"MBD4, MED1"	Methyl-CpG-binding domain protein 4	MBD4	8930	ENSG00000129071			Mbd4 (MGI:1333850)			
chr3	129440035	129520506	3q21	3q21.3-q22.1		606045	"IFT122, WDR10, CED1"	"Intraflagellar transport 122, homolog of"	IFT122	55764	ENSG00000163913		"Cranioectodermal dysplasia 1, 218330 (3), Autosomal recessive"	Ift122 (MGI:1932386)			
chr3	129500000	149200000	3q22-q24			611155	AD15	Alzheimer disease 15		100188838		max lod at D3S1579	"{Alzheimer disease-15}, 611155 (2)"				
chr3	129500000	139000000	3q22			606012	DFNA18	"Deafness, autosomal dominant 18"	DFNA18	85507			"Deafness, autosomal dominant 18, 606012 (2), Autosomal dominant"				
chr3	129500000	149200000	3q22-q24			220200	"DWS, C3DELq22q24, DEL3q22q24"	Dandy-Walker syndrome	DWS	1858		ZIC1 and ZIC4 good candidate genes	"Dandy-Walker syndrome, 220200 (4), Isolated cases"				
chr3	129500000	149200000	3q22-q24			608787	OTSC5	Otosclerosis 5	OTSC5	317682		max lod at D3S1569	"Otosclerosis 5, 608787 (2)"				
chr3	129500000	161000000	3q22-q25			173865	PABPL1	Polyadenylate-binding protein-like 1									
chr3	129500000	139000000	3q22			616361	PARK21	Parkinson disease 21		108353827		conflicting mapping on 20pter-p12	"Parkinson disease 21, 616361 (2), Autosomal dominant"				
chr3	129500000	139000000	3q22			606995	SLSN3	Senior-Loken syndrome 3		260432		?allelic with NPHP3	"Senior-Loken syndrome 3, 606995 (2), Autosomal recessive"				
chr3	129528638	129535343	3q21-q24	3q22.1		180380	"RHO, RP4, OPN2, CSNBAD1"	Rhodopsin (opsin 2)	RHO	6010	ENSG00000163914		"Night blindness, congenital stationary, autosomal dominant 1, 610445 (3); Retinitis pigmentosa 4, autosomal dominant or recessive, 613731 (3), Autosomal recessive, Autosomal dominant; Retinitis punctata albescens, 136880 (3), Autosomal recessive, Autosomal dominant"	Rho (MGI:97914)			
chr3	129555212	129606738	3q22	3q22.1		604282	PLXND1	Plexin D1	PLXND1	23129	ENSG00000004399			Plxnd1 (MGI:2154244)			
chr3	129647791	129893602	3q22.1	3q22.1		616242	"TMCC1, KIAA0779"	Transmembrane and coiled-coil domain family 1	TMCC1	23023	ENSG00000172765			Tmcc1 (MGI:2442368)			
chr3	129974392	129977937	3q13.3-q21	3q22.1		613879	TRH	Thyrotropin-releasing hormone	TRH	7200	ENSG00000170893		"Thyrotropin-releasing hormone deficiency, 275120 (1), Autosomal recessive"	Trh (MGI:98823)			
chr3	130212819	130273805	3q21	3q22.1		616612	COL6A4P2	"Collagen, type VI, alpha-4, pseudogene 2"	COL6A4P2	646300							
chr3	130345515	130484845	3q21	3q22.1		611916	"COL6A5, COL29A1"	"Collagen, type VI, alpha-5"	COL6A5	256076	ENSG00000172752			Col6a5 (MGI:3648134)			
chr3	130516708	130678136	3q21	3q22.1		616613	COL6A6	"Collagen, type VI, alpha-6"	COL6A6	131873	ENSG00000206384			Col6a6 (MGI:2444259)			
chr3	130678933	130746851	3q22.1	3q22.1		602610	PIK3R4	"Phosphatidylinositol 3-kinase, regulatory subunit 4"	PIK3R4	30849	ENSG00000196455			Pik3r4 (MGI:1922919)			
chr3	130850499	131016711	3q21-q24	3q22.1		604384	"ATP2C1, BCPM, HHD"	"ATPase, Ca(2+)-sequestering"	ATP2C1	27032	ENSG00000017260		"Hailey-Hailey disease, 169600 (3), Autosomal dominant"	Atp2c1 (MGI:1889008)			
chr3	131026849	131350464	3q21-q22	3q22.1		609779	NEK11	Never in mitosis gene A-related kinase 11	NEK11	79858	ENSG00000114670			Nek11 (MGI:2442276)			
chr3	131381670	131388829	3q22.1	3q22.1		617381	NUDT16	Nudix hydrolase 16	NUDT16	131870	ENSG00000198585			Nudt16 (MGI:1922936)			
chr3	131462200	131503015	3q22.1	3q22.1		607118	"MRPL3, MRL3, COXPD9"	Mitochondrial ribosomal protein L3	MRPL3	11222	ENSG00000114686		"Combined oxidative phosphorylation deficiency 9, 614582 (3), Autosomal recessive"	Mrpl3 (MGI:2137204)			
chr3	131533559	132285695	3q22.1	3q22.1		604208	"CPNE4, CPN4"	Copine IV	CPNE4	131034	ENSG00000196353			Cpne4 (MGI:1921270)			
chr3	132317366	132368764	3q21-q23	3q22.1		171790	ACPP	"Acid phosphatase, prostate"	ACPP	55	ENSG00000014257			Acpp (MGI:1928480)			
chr3	132417659	132539031	3q22.1	3q22.1		614334	"DNAJC13, RME8, KIAA0678"	"DNAJ/HSP40 homolog, subfamily C, member 13"	DNAJC13	23317	ENSG00000138246			Dnajc13 (MGI:2676368)			
chr3	132558137	132660130	3q22.1	3q22.1		614288	ACAD11	"Acyl-CoA dehydrogenase family, member 11"	ACAD11	84129	ENSG00000240303			Acad11 (MGI:2143169)			
chr3	132597236	132602643	3q22	3q22.1		606065	"ACKR4, CCRL1, PPR1"	Atypical chemokine receptor 4	ACKR4	51554	ENSG00000129048			Ackr4 (MGI:2181676)			
chr3	132654445	132679785	3q22	3q22.1		610552	"UBA5, UBE1DC1, EIEE44, SCAR24"	Ubiquitin-like modifier activating enzyme 5	UBA5	79876	ENSG00000081307	mutation identified in 1 SCAR24 family	"Epileptic encephalopathy, early infantile, 44, 617132 (3), Autosomal recessive; ?Spinocerebellar ataxia, autosomal recessive 24, 617133 (3), Autosomal recessive"	Uba5 (MGI:1913913)			
chr3	132680608	132722458	3q22	3q22.1		608002	"NPHP3, NPH3, RHPD1, MKS7"	Nephrocystin 3	NPHP3	27031	ENSG00000113971		"Meckel syndrome 7, 267010 (3), Autosomal recessive; Nephronophthisis 3, 604387 (3), Autosomal recessive; Renal-hepatic-pancreatic dysplasia 1, 208540 (3), Autosomal recessive"	Nphp3 (MGI:1921275)			
chr3	133038287	133397774	3q22.1	3q22.1		617361	"TMEM108, RTLN, KIAA1690"	Transmembrane protein 108	TMEM108	66000	ENSG00000144868			Tmem108 (MGI:1932411)			
chr3	133397881	133475211	3q21-q25	3q22.1		603212	"BFSP2, CP49, CP47, CTRCT12"	"Beaded filament structural protein 2 (cytoskeletal protein, 49 kD)"	BFSP2	8419	ENSG00000170819		"Cataract 12, multiple types, 611597 (3), Autosomal dominant"	Bfsp2 (MGI:1333828)			
chr3	133600604	133661967	3q22.1	3q22.1		607760	"TOPBP1, KIAA0259"	DNA topoisomerase II-binding protein 1	TOPBP1	11073	ENSG00000163781			Topbp1 (MGI:1920018)			
chr3	133661985	133779005	3q21	3q22.1		190000	"TF, TFQTL1"	Transferrin	TF	7018	ENSG00000091513		"Atransferrinemia, 209300 (3), Autosomal recessive"	Trf (MGI:98821)			
chr3	133784032	133821491	3q22.1	3q22.1		616883	"SRPRB, APMCF1"	"Signal recognition particle receptor, beta subunit"	SRPRB	58477	ENSG00000144867			Srprb (MGI:102964)			
chr3	133824234	133895846	3q22.1	3q22.1		615852	RAB6B	Ras-associated protein RAB6B	RAB6B	51560	ENSG00000154917			Rab6b (MGI:107283)			
chr3	133932695	134030075	3q21	3q22.1-q22.2		601460	"SLCO2A1, OATP2A1, PGT, SLC21A2, PHOAR2"	"Solute carrier organic anion transporter family, member 2A1"	SLCO2A1	6578	ENSG00000174640		"Hypertrophic osteoarthropathy, primary, autosomal recessive 2, 614441 (3), Autosomal recessive"	Slco2a1 (MGI:1346021)			
chr3	134157132	134250833	3q22.2	3q22.2		600524	"RYK, RYK1"	RYK receptor-like tyrosine kinase	RYK	6259	ENSG00000163785			Ryk (MGI:101766)			
chr3	134355344	134375416	3q22.2	3q22.2		614658	"AMOTL2, KIAA0989"	Angiomotin-like 2	AMOTL2	51421	ENSG00000114019			Amotl2 (MGI:1929286)			
chr3	134477703	134486022	3q22.2	3q22.2		614484	"ANAPC13, APC13, SWM1"	"Anaphase-promoting complex, subunit 13"	ANAPC13	25847	ENSG00000129055			Anapc13 (MGI:1916260)			
chr3	134485723	134783168	3q22.2	3q22.2		614724	"CEP63, SCKL6"	"Centrosomal protein, 63kD"	CEP63	80254	ENSG00000182923	mutation identified in 1 family	"?Seckel syndrome 6, 614728 (3), Autosomal recessive"	Cep63 (MGI:2158560)			
chr3	134595263	135260466	3q21-q23	3q22.2		600600	"EPHB1, EPHT2, NET"	eph tyrosine kinase 2 (ephrin receptor EphB1)	EPHB1	2047	ENSG00000154928			Ephb1 (MGI:1096337)			
chr3	134599922	134656052	3q21	3q22.2		605739	"KY, MFM7"	Kyphoscoliosis peptidase	KY	339855	ENSG00000174611		"Myopathy, myofibrillar, 7, 617114 (3), Autosomal recessive"	Ky (MGI:96709)			
chr3	135965672	136149614	3q22	3q22.2-q22.3		604944	"PP2R3A, PR72, PR130"	"Protein phosphatase 2, regulatory subunit B'', alpha"	PPP2R3A	5523	ENSG00000073711			Ppp2r3a (MGI:2442104)			
chr3	136148917	136197299	3q22.3	3q22.3		614802	"MSL2, KIAA1585"	"Male-specific lethal 2, Drosophila, homolog of"	MSL2	55167	ENSG00000174579			Msl2 (MGI:1925103)			
chr3	136250324	136330170	3q21-q22	3q22.3		232050	PCCB	"Propionyl Coenzyme A carboxylase, beta polypeptide"	PCCB	5096	ENSG00000114054	pccB complementation group	"Propionicacidemia, 606054 (3), Autosomal recessive"	Pccb (MGI:1914154)			
chr3	136336234	136752411	3q22.3	3q22.3		604358	"STAG1, MRD47"	Stromal antigen 1	STAG1	10274	ENSG00000118007		"Mental retardation, autosomal dominant 47, 617635 (3), Autosomal dominant"	Stag1 (MGI:1098658)			
chr3	136819018	136855891	3q22.3	3q22.3		617812	"SLC35G2, TMEM22"	"Solute carrier family 35, member G2"	SLC35G2	80723	ENSG00000168917			Slc35g2 (MGI:2685365)			
chr3	136862207	136951609	3q21	3q22.3		600508	NCK	Non-catalytic region of tyrosine kinase	NCK1	4690	ENSG00000158092			Nck1 (MGI:109601)			
chr3	137764291	137766333	3q23	3q22.3		604747	SOX14	SRY-box 14	SOX14	8403	ENSG00000168875			Sox14 (MGI:98362)			
chr3	138061984	138115861	3q22.3	3q22.3		617570	"DZIP1L, DZIP2, PKD5"	DAZ-interacting zinc finger protein 1-like	DZIP1L	199221	ENSG00000158163		"Polycystic kidney disease 5, 617610 (3), Autosomal recessive"	Dzip1l (MGI:1919757)			
chr3	138123717	138133309	3p14.3	3q22.3		616709	A4GNT	"Alpha-1,4-N-acetylglucosaminyltransferase"	A4GNT	51146	ENSG00000118017			A4gnt (MGI:2143261)			
chr3	138160987	138174948	3q22.3	3q22.3		607024	DBR1	"Debranching enzyme 1, S. cerevisiae, homolog of"	DBR1	51163	ENSG00000138231			Dbr1 (MGI:1931520)			
chr3	138347647	138405534	3q22.3	3q22.3		608435	"MRAS, RRAS3"	Muscle Ras viral oncogene homolog	MRAS	22808	ENSG00000158186			Mras (MGI:1100856)			
chr3	138434572	138479941	3q22.3	3q22.3		616692	"ESYT3, FAM62C"	Extended synaptotagmin-like protein 3	ESYT3	83850	ENSG00000158220			Esyt3 (MGI:1098699)			
chr3	138494338	138594382	3q22.3	3q22.3		614310	CEP70	"Centrosomal protein, 70kD"	CEP70	80321	ENSG00000114107			Cep70 (MGI:1915371)			
chr3	138608098	138633375	3q22	3q22.3		617535	FAIM	Fax apoptotic inhibitory molecule	FAIM	55179	ENSG00000158234			Faim (MGI:1344387)			
chr3	138652697	138834937	3q22.3	3q22.3		602925	"PIK3CB, PI3KCB"	"Phosphatidylinositol 3-kinase, catalytic, beta"	PIK3CB	5291	ENSG00000051382			Pik3cb (MGI:1922019)			
chr3	138944223	138947139	3q23	3q22.3		605597	"FOXL2, BPES, BPES1, PFRK, POF3"	Forkhead transcription factor FOXL2	FOXL2	668	ENSG00000183770		"Blepharophimosis, epicanthus inversus, and ptosis, type 1, 110100 (3), Autosomal dominant; Blepharophimosis, epicanthus inversus, and ptosis, type 2, 110100 (3), Autosomal dominant; Premature ovarian failure 3, 608996 (3), Autosomal dominant"	Foxl2 (MGI:1349428)			
chr3	139000000	143100000	3q23			612221	STQTL10	Stature quantitative trait locus 10		100270794		associated with rs6440003	"{Stature QTL 10}, 612221 (2)"				
chr3	139344013	139357128	3q23	3q23		605810	"MRPS22, C3orf5, COXPD5"	Mitochondrial ribosomal protein S22	MRPS22	56945	ENSG00000175110		"Combined oxidative phosphorylation deficiency 5, 611719 (3), Autosomal recessive"	Mrps22 (MGI:1928137)			
chr3	139355594	139389679	3q23	3q23		606990	"COPB2, MCPH19"	"Coatomer protein complex, subunit beta-2"	COPB2	9276	ENSG00000184432	mutation identified in 1 MCPH19 family	"?Microcephaly 19, primary, autosomal recessive, 617800 (3), Autosomal recessive"	Copb2 (MGI:1354962)			
chr3	139452883	139476509	3q21-qter	3q23		180280	"RBP2, CRBP2"	"Retinol-binding protein-2, cellular"	RBP2	5948	ENSG00000114113	close to CRBP1		Rbp2 (MGI:97877)			
chr3	139517433	139539828	3q21-q22	3q23		180260	"RBP1, CRBP1"	"Retinol-binding protein-1, cellular"	RBP1	5947	ENSG00000114115	close to CRBP2		Rbp1 (MGI:97876)			
chr3	139560179	139678049	3q23	3q23		608702	"NMNAT3, PNAT3"	Nicotinamide nucleotide adenylyltransferase 3	NMNAT3	349565	ENSG00000163864						
chr3	139935184	140577396	3q23	3q23		611323	CLSTN2	Calsyntenin 2	CLSTN2	64084	ENSG00000158258			Clstn2 (MGI:1929897)			
chr3	140941819	140979942	3q23	3q23		616149	"SLC25A36, PNC2"	"Solute carrier family 25 (mitochondrial carrier, pyrimidine nucleotide transporter), member 36"	SLC25A36	55186	ENSG00000114120			Slc25a36 (MGI:1924909)			
chr3	141051401	141148610	3q23	3q23		611660	"SPSB4, SSB4"	SPRY domain- and SOCS box-containing 4	SPSB4	92369	ENSG00000175093			Spsb4 (MGI:2183445)			
chr3	141324212	141449791	3q23	3q23		612218	ZBTB38	Zinc finger- and BTB domain-containing protein 38	ZBTB38	253461	ENSG00000177311			Zbtb38 (MGI:2442866)			
chr3	141487046	141615362	3q22-q23	3q23		601589	"RASA2, GAP1M"	RAS p21 protein activator 2	RASA2	5922	ENSG00000155903			Rasa2 (MGI:2149960)			
chr3	141738208	141746802	3q22-q24	3q23		603863	"RNF7, ROC2, SAG"	RING finger protein-7 (regulator of cullins 2; sensitive to apoptosis gene)	RNF7	9616	ENSG00000114125			Rnf7 (MGI:1337096)			
chr3	141763123	141818489	3q21-q23	3q23		606987	"GRK7, GPRK7"	G protein-coupled receptor kinase 7	GRK7	131890	ENSG00000114124						
chr3	141876591	141926547	3q22-q23	3q23		601867	ATP1B3	"ATPase, Na+/K+ transporting, beta 3 polypeptide"	ATP1B3	483	ENSG00000069849			Atp1b3 (MGI:107788)			
chr3	141944427	142149543	3q23	3q23		602160	"TFDP2, DP2"	Transcription factor Dp-2 (E2F dimerization partner 2)	TFDP2	7029	ENSG00000114126			Tfdp2 (MGI:107167)			
chr3	142306606	142448061	3q25-q26.1	3q23		607994	"XRN1, SEP1"	Exoribonuclease 1	XRN1	54464	ENSG00000114127			Xrn1 (MGI:891964)			
chr3	142449234	142578825	3q22-q24	3q23		601215	"ATR, FRP1, SCKL1, FCTCS"	Ataxia-telangiectasia and Rad3-related (FRAP-related protein-1)	ATR	545	ENSG00000175054	mutation identified in 1 FCTCS family	"?Cutaneous telangiectasia and cancer syndrome, familial, 614564 (3), Autosomal dominant; Seckel syndrome 1, 210600 (3), Autosomal recessive"	Atr (MGI:108028)			
chr3	142596386	142713663	3q23	3q23		602734	PLS1	Plastin-1	PLS1	5357	ENSG00000120756			Pls1 (MGI:104809)			
chr3	142724423	142807887	3q22-q24	3q23		602343	"TRPC1, TRP1"	Transient receptor potential channel 1	TRPC1	7220	ENSG00000144935	also called Htrp-1		Trpc1 (MGI:109528)			
chr3	142817859	142889202	3q21-q24	3q23		607064	PCOLCE2	Procollagen C-endopeptidase enhancer-2	PCOLCE2	26577	ENSG00000163710			Pcolce2 (MGI:1923727)			
chr3	142961230	142963335	3q23	3q23		614580	PAQR9	"Progestin and ADIPOQ receptor family, member 9"	PAQR9	344838	ENSG00000188582			Paqr9 (MGI:1922802)			
chr3	143001529	143060724	3q23	3q23		617849	"U2SURP, SR140, KIAA0332"	U2 small nuclear ribonucleoprotein-associated SURP domain-containing protein	U2SURP	23350	ENSG00000163714			U2surp (MGI:1915208)			
chr3	143100000	183000000	3q24-q26			610761	HDLCQ5	High density lipoprotein cholesterol level QTL 5		100188818		max lod at D3S3053	"[High density lipoprotein cholesterol level QTL 5], 610761 (2)"				
chr3	143100000	183000000	3q24-q26			606660	UVM1	"Melanoma, uveal, susceptibility to, 1"		170592			"{Melanoma, uveal, susceptibility to, 1}, 606660 (2)"				
chr3	143119775	143124013	3q24	3q24		603798	CHST2	Carbohydrate sulfotransferase-2 (GlcNAc-6-O-sulfotransferase; N-acetylglucosamine-6-O-sulfotransferase)	CHST2	9435	ENSG00000175040	mapped by FISH to 7q31		Chst2 (MGI:1891160)			
chr3	143265221	143848530	3q24	3q24		608396	"SLC9A9, AUTS16"	"Solute carrier family 9 (sodium/hydrogen exchanger), member A9"	SLC9A9	285195	ENSG00000181804	mutation identified in 1 family	"{?Autism susceptibility 16}, 613410 (3)"	Slc9a9 (MGI:2679732)			
chr3	143971797	143992367	3q24	3q24		612200	"C3orf58, DIA1"	Chromosome 3 open reading frame 58	C3orf58	205428	ENSG00000181744			1190002N15Rik (MGI:1916111)			
chr3	146069436	146161494	3q23-q24	3q24		601865	"PLOD2, LH2, TLH, BRKS2"	"Procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2"	PLOD2	5352	ENSG00000152952		"Bruck syndrome 2, 609220 (3), Autosomal recessive"	Plod2 (MGI:1347007)			
chr3	146192334	146251178	3q23	3q24		607612	PLSCR4	Phospholipid scramblase 4	PLSCR4	57088	ENSG00000114698			Plscr4 (MGI:2143267)			
chr3	146391362	146497162	3q23	3q24		607610	PLSCR2	Phospholipid scramblase 2	PLSCR2	57047	ENSG00000163746						
chr3	146515177	146544840	3q23	3q24		604170	"PLSCR1, MMTRA1B"	Phospholipid scramblase 1	PLSCR1	5359	ENSG00000188313			Plscr1 (MGI:893575)			
chr3	147386047	147407475	3q24	3q24		608948	ZIC4	"Zic family, member 4"	ZIC4	84107	ENSG00000174963			Zic4 (MGI:107201)			
chr3	147409393	147416718	3q24	3q24		600470	"ZIC1, CRS6"	"Zic family, member 1"	ZIC1	7545	ENSG00000152977		"Craniosynostosis 6, 616602 (3), Autosomal dominant"	Zic1 (MGI:106683)			
chr3	148697870	148743002	3q21-q25	3q24		106165	"AGTR1, AGTR1A, AT2R1"	Angiotensin receptor 1	AGTR1	185	ENSG00000144891		"{Hypertension, essential}, 145500 (3), Multifactorial; Renal tubular dysgenesis, 267430 (3), Autosomal recessive"	Agtr1a (MGI:87964)			
chr3	148827800	148860186	3q24	3q24		114852	"CPB1, PCPB, PASP"	"Carboxypeptidase B1, tissue"	CPB1	1360	ENSG00000153002			Cpb1 (MGI:1923953)			
chr3	148865255	148897090	3q24	3q24		114851	CPA3	"Carboxypeptidase A3, mast cell"	CPA3	1359	ENSG00000163751			Cpa3 (MGI:88479)			
chr3	148991407	149027668	3q24-q25.1	3q24		603942	"GYG1, GSD15"	Glycogenin 1	GYG1	2992	ENSG00000163754	mutation identified in 1 GSD15 patient	"?Glycogen storage disease XV, 613507 (3), Autosomal recessive; Polyglucosan body myopathy 2, 616199 (3), Autosomal recessive"	Gyg (MGI:1351614)			
chr3	149030063	149086553	3q25.1-q26.1	3q24		603257	"SMARCA3, SNF2L3, HIP116"	"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 3"	HLTF	6596	ENSG00000071794			Hltf (MGI:1196437)			
chr3	149129583	149173195	3q24	3q24		606118	HPS3	HPS gene 3	HPS3	84343	ENSG00000163755		"Hermansky-Pudlak syndrome 3, 614072 (3), Autosomal recessive"	Hps3 (MGI:2153839)			
chr3	149162409	149222044	3q23-q24	3q24-q25		117700	CP	Ceruloplasmin	CP	1356	ENSG00000047457	~15cM from TF	"Cerebellar ataxia, 604290 (3), Autosomal recessive; Hemosiderosis, systemic, due to aceruloplasminemia, 604290 (3), Autosomal recessive; [Hypoceruloplasminemia, hereditary], 604290 (3), Autosomal recessive"	Cp (MGI:88476)			
chr3	149200000	188200000	3q25-q27			608638	ASPG1	"Asperger syndrome, susceptibility to, 1"		431710		max lod with D3S3037	"{Asperger syndrome susceptibility 1}, 608638 (2), Isolated cases, Multifactorial"				
chr3	149200000	188200000	3q25-q27			607373	AUTS8	"Autism, susceptibility to, 8"		282553			"{Autism susceptibility 8}, 607373 (2), Isolated cases, Multifactorial"				
chr3	149200000	183000000	3q25-q26			612008	CELIAC10	"Celiac disease, susceptibility to, 10"		100188872		associated with rs17810546	"{Celiac disease, susceptibility to, 10}, 612008 (2)"				
chr3	149200000	183000000	3q25-q26			615697	ETL6	"Epilepsy, familial temporal lobe, 6"		103106902		between D3S1584 and D3S3520	"Epilepsy, familial temporal lobe, 6, 615697 (2)"				
chr3	149369017	149377780	3q21-q25	3q25.1		191155	"TM4SF1, M3S1, TAAL6"	"Transmembrane-4 superfamily, member 1"	TM4SF1	4071	ENSG00000169908			Tm4sf1 (MGI:104678)			
chr3	149474580	149503393	3q25	3q25.1		606567	"TM4SF4, ILTMP"	"Transmembrane 4 superfamily, member 4"	TM4SF4	7104	ENSG00000169903			Tm4sf4 (MGI:2385173)			
chr3	149517228	149724787	3q24	3q25.1		607392	"WWTR1, TAZ"	WW domain-containing transcription regulator 1	WWTR1	25937	ENSG00000018408			Wwtr1 (MGI:1917649)			
chr3	149738469	149752498	3q25.1	3q25.1		616699	COMMD2	COMM domain-containing protein 2	COMMD2	51122	ENSG00000114744			Commd2 (MGI:1098806)			
chr3	149964903	149970953	3q25.1-q25.2	3q25.1		176590	"PFN2, PFL, D3S1319E"	Profilin-2	PFN2	5217	ENSG00000070087	mapped previously to chr.1		Pfn2 (MGI:97550)			
chr3	149981660	149983365	3q25.1	3q25.1		611365	"TMEM183B, C1orf37DUP"	Transmembrane protein 183B	TMEM183B	653659							
chr3	150408334	150460118	3q25.1	3q25.1		617724	"TSC22D2, KIAA0669"	"TSC22 domain family, member 2"	TSC22D2	9819	ENSG00000196428			Tsc22d2 (MGI:1919283)			
chr3	150541992	150546640	3q25.1	3q25.1		617674	"SERP1, RAMP4"	Stress-associated endoplasmic reticulum protein 1	SERP1	27230	ENSG00000120742			Serp1 (MGI:92638)			
chr3	150546677	150586015	3q25.1	3q25.1		609234	EIF2A	Eukaryotic translation initiation factor 2A	EIF2A	83939	ENSG00000144895			Eif2a (MGI:1098684)			
chr3	150603262	150630446	3q24	3q25.1		607912	"SELENOT, SELT"	Selenoprotein T	SELENOT	51714	ENSG00000198843			Selenot (MGI:1916477)			
chr3	150741122	150763147	3q25	3q25.1		602213	SIAH2	"Seven in absentia, Drosophila, homolog of, 2"	SIAH2	6478	ENSG00000181788			Siah2 (MGI:108062)			
chr3	150926162	150972998	3q21-q25	3q25.1		606397	"CLRN1, USH3A, USH3, RP61"	Clarin 1	CLRN1	7401	ENSG00000163646	frequent in Finland; ?digenic interaction with MYO7A	"Retinitis pigmentosa 61, 614180 (3); Usher syndrome, type 3A, 276902 (3), Autosomal recessive"	Clrn1 (MGI:2388124)			
chr3	151085664	151436676	3q21-q25	3q25.1		611318	"MED12L, NOPAR, KIAA1635"	Mediator complex subunit 12-like	MED12L	116931	ENSG00000144893			Med12l (MGI:2139916)			
chr3	151212114	151279166	3q25.1	3q25.1		610116	"P2RY14, BPR105, KIAA0001"	"Purinergic receptor P2Y, G protein-coupled, 14"	P2RY14	9934	ENSG00000174944			P2ry14 (MGI:2155705)			
chr3	151294085	151316847	3q24	3q25.1		606379	GPR87	G protein-coupled receptor 87	GPR87	53836	ENSG00000138271			Gpr87 (MGI:1934133)			
chr3	151326307	151329548	3q24	3q25.1		606380	GPR86	G protein-coupled receptor 86	P2RY13	53829	ENSG00000181631			P2ry13 (MGI:1921441)			
chr3	151336842	151384811	3q24-q25	3q25.1		600515	"P2RY12, P2Y12, BDPLT8"	"Purinergic receptor P2Y, G protein-coupled, 12"	P2RY12	64805	ENSG00000169313		"Bleeding disorder, platelet-type, 8, 609821 (3), Autosomal recessive"	P2ry12 (MGI:1918089)			
chr3	151435050	151619925	3q25.1	3q25.1		617351	IGSF10	"Immunoglobulin superfamily, member 10"	IGSF10	285313	ENSG00000152580			Igsf10 (MGI:1923481)			
chr3	151814007	151828487	3q21.3-q25.2	3q25.1		600338	"AADAC, DAC"	Arylacetamide deacetylase (esterase)	AADAC	13	ENSG00000114771			Aadac (MGI:1915008)			
chr3	151873642	151884618	3q24-q25.1	3q25.1		606381	"SUCNR1, GPR91"	Succinate receptor 1	SUCNR1	56670	ENSG00000198829			Sucnr1 (MGI:1934135)			
chr3	152243655	152465779	3q25	3q25.1-q25.2		606516	"MBNL1, KIAA0428, EXP"	Muscleblind-like protein	MBNL1	4154	ENSG00000152601			Mbnl1 (MGI:1928482)			
chr3	152834692	152841438	3q25	3q25.2		601167	"P2RY1, P2Y1"	"Purinergic receptor P2Y, G-protein coupled, 1"	P2RY1	5028	ENSG00000169860			P2ry1 (MGI:105049)			
chr3	153162211	153170623	3q25.2	3q25.2		179541	RAP2B	Ras-related protein 2B	RAP2B	5912	ENSG00000181467			Rap2b (MGI:1921262)			
chr3	154121002	154257826	3q25.2	3q25.2		617552	"ARHGEF26, SGEF"	Rho guanine nucleotide exchange factor 26	ARHGEF26	26084	ENSG00000114790			Arhgef26 (MGI:1918053)			
chr3	154271827	154324496	3q25.2	3q25.2		612767	"DHX36, G4R1, RHAU, KIAA1488"	DEAH (Asp-Glu-Ala-His) box polypeptide 36	DHX36	170506	ENSG00000174953			Dhx36 (MGI:1919412)			
chr3	155024123	155183728	3q21-q27	3q25.2		120520	"MME, CD10, CALLA, NEP, CMT2T, SCA43"	Membrane metallo-endopeptidase (common acute lymphocytic leukemia antigen)	MME	4311	ENSG00000196549	mutation identified in 1 SCA43 family	"Charcot-Marie-Tooth disease, axonal, type 2T, 617017 (3), Autosomal recessive, Autosomal dominant; ?Spinocerebellar ataxia 43, 617018 (3), Autosomal dominant"	Mme (MGI:97004)			
chr3	155290231	155293699	3q25.2	3q25.2		616891	"DWORF, LOC100507537"	Dwarf open reading frame		100507537	ENSG00000240045						
chr3	155300000	161000000	3q25.3			613459	BWQTL2	Birth weight quantitative trait locus 2		100502569		associated with rs900400	"[Birth weight QTL 2], 613459 (2)"				
chr3	155458602	155745723	3q25.31	3q25.31		612835	"PLCH1, PLCL3, KIAA1069"	"Phospholipase C, eta-1"	PLCH1	23007	ENSG00000114805			Plch1 (MGI:2683547)			
chr3	155826510	155855357	3q25.31	3q25.31		603690	"SLC33A1, ACATN, AT1, SPG42, CCHLND"	"Solute carrier family 33 (acetyl-CoA transporter), member 1"	SLC33A1	9197	ENSG00000169359		"Congenital cataracts, hearing loss, and neurodegeneration, 614482 (3), Autosomal recessive; Spastic paraplegia 42, autosomal dominant, 612539 (3), Autosomal dominant"	Slc33a1 (MGI:1332247)			
chr3	155869429	155943678	3q24	3q25.31		600358	GMPS	Guanine monophosphate synthetase	GMPS	8833	ENSG00000163655	fusion gene with MLL in AML		Gmps (MGI:2448526)			
chr3	156118215	156542647	3q26.1	3q25.31		601141	"KCNAB1, KCNA1B"	"Potassium voltage-gated channel, shaker-related subfamily, beta member 1"	KCNAB1	7881	ENSG00000169282			Kcnab1 (MGI:109155)			
chr3	156539552	156555199	3q25.31	3q25.31		606213	"SSR3, TRAPG"	"Signal sequence receptor, gamma"	SSR3	6747	ENSG00000114850			Ssr3 (MGI:1914687)			
chr3	156674415	156706769	3q25.31	3q25.31		612480	TIPARP	TCDD-inducible poly(ADP-ribose) polymerase	TIPARP	25976	ENSG00000163659			Tiparp (MGI:2159210)			
chr3	156826286	157047658	3q25.31	3q25.31		613536	LEKR1	"Leucine-, glutamate-, and lysine-rich protein 1"	LEKR1	389170	ENSG00000197980			Lekr1 (MGI:3645902)			
chr3	157146501	157160759	3q25.31	3q25.31		613384	"CCNL1, ANIA6A"	Cyclin L1	CCNL1	57018	ENSG00000163660			Ccnl1 (MGI:1922664)			
chr3	157259741	157503776	3q24-q25	3q25.31-q25.32		609594	"VEPH1, MELT, KIAA1692"	"Ventricular zone-expressed PH domain-containing protein, zebrafish, homolog of, 1"	VEPH1	79674	ENSG00000197415			Veph1 (MGI:1920039)			
chr3	157436790	157443627	3q25	3q25.32		602492	PTX3	Pentraxin-3	PTX3	5806	ENSG00000163661			Ptx3 (MGI:104641)			
chr3	158096010	158106211	3q25-q26	3q25.32		602504	"SHOX2, SHOT, OG12"	Short stature homeo box 2	SHOX2	6474	ENSG00000168779			Shox2 (MGI:1201673)			
chr3	158110051	158544834	3q25.32	3q25.32		613352	"RSRC1, SRRP53"	Arginine/serine-rich coiled-coil protein 1	RSRC1	51319	ENSG00000174891			Rsrc1 (MGI:1914130)			
chr3	158571162	158606459	3q25.1	3q25.32		601402	MLF1	Myeloid leukemia factor-1	MLF1	4291	ENSG00000178053		"Leukemia, acute myeloid, 601626 (1), Autosomal dominant"	Mlf1 (MGI:1341819)			
chr3	158644523	158692571	3q25.32	3q25.32		606639	"GFM1, EFG1, GFM, COXPD1"	Mitochondrial elongation factor G1	GFM1	85476	ENSG00000168827		"Combined oxidative phosphorylation deficiency 1, 609060 (3), Autosomal recessive"	Gfm1 (MGI:107339)			
chr3	158666413	158672721	3q25.3	3q25.32		609305	"LXN, ECI, TCI"	Latexin	LXN	56925	ENSG00000079257			Lxn (MGI:107633)			
chr3	158696891	158732943	3q25.3	3q25.32		605090	"RARRES1, TIG1"	Retinoic acid receptor responder 1	RARRES1	5918	ENSG00000118849			Rarres1 (MGI:1924461)			
chr3	159069251	159266306	3q25	3q25.32		611622	IQCJ	IQ motif-containing protein J	IQCJ	654502	ENSG00000214216			Iqcj (MGI:3644166)			
chr3	159988835	159996018	3p12-q13.2	3q25.33		161560	IL12A	"Interleukin-12A (natural killer cell stimulatory factor-1, cytotoxic lymphocyte maturation factor-1, p35)"	IL12A	3592	ENSG00000168811			Il12a (MGI:96539)			
chr3	160256985	160399531	3q25.33	3q25.33		611177	"IFT80, KIAA1374, WDR56, SRTD2, ATD2"	"Intraflagellar transport 80, Chlamydomonas, homolog of"	IFT80	57560	ENSG00000068885		"Short-rib thoracic dysplasia 2 with or without polydactyly, 611263 (3), Autosomal recessive"	Ift80 (MGI:1915509)			
chr3	160399303	160434961	3q26.1	3q25.33		605575	CAPC	Chromosome-associated protein C	SMC4	10051	ENSG00000113810			Smc4 (MGI:1917349)			
chr3	160435502	160449837	3q26.1	3q25.33		616148	"TRIM59, RNF104, MRF1, IFT80L"	Tripartite motif-containing protein 59	TRIM59	286827	ENSG00000213186			Trim59 (MGI:1914199)			
chr3	160494994	160565587	3q26.1	3q25.33		602970	"KPNA4, QIP1"	Karyopherin alpha-4	KPNA4	3840	ENSG00000186432			Kpna4 (MGI:1100848)			
chr3	160514906	160515235	3q25.33	3q25.33		615644	SCARNA7	Small Cajal body-specific RNA 7	SCARNA7	677767							
chr3	160677159	160678447	3q25.33	3q25.33		614439	"ARL14, ARF7"	ADP-ribosylation factor-like 14	ARL14	80117	ENSG00000179674			Arl14 (MGI:1918869)			
chr3	160755531	161078906	3q26.1	3q25.3-q26.1		611931	"PPM1L, PP2CE"	Protein phosphatase 1-like	PPM1L	151742	ENSG00000163590			Ppm1l (MGI:2139740)			
chr3	161000000	183000000	3q26			109200	"AGA1, MPB"	"Alopecia, androgenetic, 1"		100188784			"Alopecia, androgenetic, 1, 109200 (2), Autosomal dominant"				
chr3	161000000	183000000	3q26			600049	MDS1	Myelodysplasia syndrome-1				cen--EVI1--MDS1--EAP--tel	Myelodysplasia syndrome-1 (3)				
chr3	161000000	183000000	3q26.1-q26.3			606082	MNG3	Multinodular goiter-3		94337			"Goiter, multinodular, 3, 606082 (2)"				
chr3	161000000	183000000	3q26			609257	MYP8	Myopia 8	MYP8	553192			"Myopia 8, 609257 (2), Multifactorial"				
chr3	161083882	161105468	3q25	3q26.1		603094	"B3GALT3, GLCT3, GLOB"	"UDP-galactose:beta-N-acetylglucosamine beta-1,3-galactosyltransferase 3"	B3GALNT1	8706	ENSG00000169255		"[Blood group, P1PK system, P(k) phenotype], 111400 (3); [Blood group, globoside system], 615021 (3)"	B3galnt1 (MGI:1349405)			
chr3	161221289	161253531	3q26.1	3q26.1		611021	NMD3	"NMD3, S. cerevisiae, homolog of"	NMD3	51068	ENSG00000169251			Nmd3 (MGI:2140103)			
chr3	161344783	161373227	3q26.1	3q26.1		610412	"SPTSSB, C3orf57, SSSPTB, ADMP"	"Serine palmitoyltransferase, small subunit B"	SPTSSB	165679	ENSG00000196542			Sptssb (MGI:1913433)			
chr3	164978897	165078494	3q25-q26	3q26.1		609845	SI	Sucrase-isomaltase	SI	6476	ENSG00000090402		"Sucrase-isomaltase deficiency, congenital, 222900 (3), Autosomal recessive"	Sis (MGI:1917233)			
chr3	165186719	165197108	3q26	3q26.1		609679	"SLITRK3, KIAA0848"	"SLIT- and NTRK-like family, member 3"	SLITRK3	22865	ENSG00000121871			Slitrk3 (MGI:2679447)			
chr3	165772902	165837471	3q26.1-q26.2	3q26.1		177400	"BCHE, CHE1"	Butyrylcholinesterase	BCHE	590	ENSG00000114200	"distal to CP, TF"	"Apnea, postanesthetic (3)"	Bche (MGI:894278)			
chr3	167441788	167474131	3q26.1-q26.2	3q26.1		605587	"SERPIN12, PI14, MEPI"	Protease inhibitor 14	SERPINI2	5276	ENSG00000114204			Serpini2 (MGI:1915181)			
chr3	167683892	167735809	3q26.1	3q26.1		609118	"PDCD10, TFAR15, CCM3"	Programmed cell death 10	PDCD10	11235	ENSG00000114209		"Cerebral cavernous malformations 3, 603285 (3)"	Pdcd10 (MGI:1928396)			
chr3	167735643	167825568	3q26	3q26.1		602445	"SERPINI1, PI12"	Protease inhibitor 12	SERPINI1	5274	ENSG00000163536		"Encephalopathy, familial, with neuroserpin inclusion bodies, 604218 (3), Autosomal dominant"	Serpini1 (MGI:1194506)			
chr3	167900000	176000000	3q26.2-q26.31			610422	APMR2	Alopecia-mental retardation syndrome 2		100049544		between D3S1564 and D3S2427	"Alopecia-mental retardation syndrome 2, 610422 (2), Autosomal recessive"				
chr3	167900000	183000000	3q26.2-q26.33			612637	10-Feb	"Febrile seizures, familial, 10"		100271923		between D3S3656 and D3S1232	"Febrile seizures, familial, 10, 612637 (2)"				
chr3	168008671	168095924	3q26.2	3q26.2		606805	"GOLIM4, GOLPH4, GPP130"	Golgi integral membrane protein 4	GOLIM4	27333	ENSG00000173905			Golim4 (MGI:1920374)			
chr3	169083498	169663780	3q26	3q26.2		165215	"MECOM, EVI1, RUSAT2"	MDS1 and EVS1 complex locus	MECOM	2122	ENSG00000085276		"Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, 616738 (3), Autosomal dominant"	Mecom (MGI:95457)			
chr3	169764609	169765059	3q21-q28	3q26.2		602322	"TERC, TRC3, TR, DKCA1, PFBMFT2"	Telomerase RNA component	TERC	7012			"{Aplastic anemia}, 614743 (3), Autosomal dominant; Dyskeratosis congenita, autosomal dominant 1, 127550 (3), Autosomal dominant; {Pulmonary fibrosis, idiopathic, susceptibility to}, 614743 (3), Autosomal dominant"				
chr3	169766920	169769894	3q26.2	3q26.2		608534	ARPM1	Actin-related protein M1	ACTRT3	84517	ENSG00000184378			Actrt3 (MGI:1923902)			
chr3	169772229	169772301	3q26.2	3q26.2		615310	"TRV-AAC1-1, TRNAV24"	Transfer RNA valine (AAC) 1-1	TRV-AAC1-1	100189318							
chr3	169772246	169790454	3q26.2	3q26.2		606042	MYNN	Myoneurin	MYNN	55892	ENSG00000085274			Mynn (MGI:1931415)			
chr3	169966135	169998372	3q26.2	3q26.2		602173	"SEC62, TLOC1, HTP1"	"Sec62, S. cerevisiae, homolog of"	SEC62	7095	ENSG00000008952			Sec62 (MGI:1916526)			
chr3	170222431	170305981	3p25-q27	3q26.2		600539	PRKCI	"Protein kinase C, iota"	PRKCI	5584	ENSG00000163558	pseudogene on X		Prkci (MGI:99260)			
chr3	170357677	170396848	3q26.2	3q26.2		165340	"SKIL, SNO"	SKI-like	SKIL	6498	ENSG00000136603			Skil (MGI:106203)			
chr3	170418864	170434690	3q26.2-q26.3	3q26.2		601326	"CLDN11, OTM, OSP"	Claudin 11 (oligodendrocyte transmembrane protein)	CLDN11	5010	ENSG00000013297			Cldn11 (MGI:106925)			
chr3	170459553	170586073	3q26.2	3q26.2		615720	"SLC7A14, KIAA1613, RP68"	"Solute carrier family 7, member 14"	SLC7A14	57709	ENSG00000013293		"Retinitis pigmentosa 68, 615725 (3), Autosomal recessive"	Slc7a14 (MGI:3040688)			
chr3	170888414	170908636	3q25-q27	3q26.2		605782	EIF5A2	Eukaryotic translation initiation factor 5A2	EIF5A2	56648	ENSG00000163577			Eif5a2 (MGI:1933735)			
chr3	170996340	171026978	3q26.1-q26.3	3q26.2		138160	"SLC2A2, GLUT2"	"Solute carrier family 2 (facilitated glucose transporter), member 2"	SLC2A2	6514	ENSG00000163581		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant; Fanconi-Bickel syndrome, 227810 (3), Autosomal recessive"	Slc2a2 (MGI:1095438)			
chr3	171058413	171460407	3q26.2-q26.3	3q26.2-q26.3		610005	"TNIK, KIAA0551, MRT54"	TRAF2-and NCK-interacting kinase	TNIK	23043	ENSG00000154310		"Mental retardation, autosomal recessive 54, 617028 (3), Autosomal recessive"	Tnik (MGI:1916264)			
chr3	171200000	188200000	3q26.3-q27.3			203650	APMR1	Alopecia-mental retardation syndrome 1				max lod at D3S3583	"Alopecia-mental retardation syndrome 1, 203650 (2), Autosomal recessive"				
chr3	171600403	171810493	3q26	3q26.31		602382	"PLD1, CVDD"	"Phospholipase D1, phosphatidylcholine-specific"	PLD1	5337	ENSG00000075651		"Cardiac valvular defect, developmental, 212093 (3), Autosomal recessive"	Pld1 (MGI:109585)			
chr3	172039627	172400702	3q26	3q26.31		611909	"FNDC3B, FAD104"	Fibronectin domain III-containing protein 3B	FNDC3B	64778	ENSG00000075420			Fndc3b (MGI:1919257)			
chr3	172443290	172448455	3q26.3	3q26.31		601898	"GHSR, GHDP"	Growth hormone secretagogue receptor	GHSR	2693	ENSG00000121853		"Growth hormone deficiency, isolated partial, 615925 (3), Autosomal recessive, Autosomal dominant"	Ghsr (MGI:2441906)			
chr3	172505507	172523506	3q26	3q26.31		603598	"TNFSF10, TRAIL, APO2L"	"Tumor necrosis factor ligand superfamily, member 10"	TNFSF10	8743	ENSG00000121858			Tnfsf10 (MGI:107414)			
chr3	172630644	172711217	3q26.3	3q26.31		613234	"NCEH1, NCEH, KIAA1363"	Neutral cholesterol ester hydrolase 1	NCEH1	57552	ENSG00000144959			Nceh1 (MGI:2443191)			
chr3	172750684	172829272	3q26.1-q26.2	3q26.31		600586	ECT2	Epithelial cell transforming sequence 2 oncogene	ECT2	1894	ENSG00000114346			Ect2 (MGI:95281)			
chr3	172889356	173141267	3q26.3	3q26.31		609856	"SPATA16, SPGF6"	Spermatogenesis-associated protein 16	SPATA16	83893	ENSG00000144962	mutation identified in 1 SPGF6 family	"?Spermatogenic failure 6, 102530 (3), Autosomal recessive"	Spata16 (MGI:1918112)			
chr3	173395898	174291286	3q26.3	3q26.31		600568	NLGN1	Neuroligin 1	NLGN1	22871	ENSG00000169760			Nlgn1 (MGI:2179435)			
chr3	174438533	175810547	3q26.3	3q26.31		608806	NAALADL2	N-acetylated alpha-linked acidic dipeptidase-like 2	NAALADL2	254827	ENSG00000177694	?involved in Cornelia de Lange syndrome		Naaladl2 (MGI:2685867)			
chr3	176000000	192600000	3q26.32-q28			615127	"FAME4, FCMTE4"	"Epilepsy, familial adult myoclonic, 4"		101409188		between D3S3730 and D3S1580	"Epilepsy, myoclonic, familial adult, 4, 615127 (2), Autosomal dominant"				
chr3	177019354	177197356	3q26.32	3q26.32		608628	"TBL1XR1, TBLR1, IRA1, C21, MRD41"	Transducin-beta-like 1 receptor 1	TBL1XR1	79718	ENSG00000177565		"Mental retardation, autosomal dominant 41, 616944 (3), Autosomal dominant; Pierpont syndrome, 602342 (3), Autosomal dominant"	Tbl1xr1 (MGI:2441730)			
chr3	178536297	178844428	3q26.32	3q26.32		605214	KCNMB2	"Potassium channel, calcium-activated, large conductance, subfamily M, beta member 2"	KCNMB2	10242	ENSG00000197584			Kcnmb2 (MGI:1919663)			
chr3	179017222	179071867	3q26.3-q27	3q26.32		606452	WIG1	Wildtype p53-induced gene	ZMAT3	64393	ENSG00000172667			Zmat3 (MGI:1195270)			
chr3	179148113	179240092	3q26.3	3q26.32		171834	"PIK3CA, CLOVE, MCAP, MCM, MCMTC, CWS5"	"Phosphatidylinositol 3-kinase, catalytic, alpha polypeptide"	PIK3CA	5290	ENSG00000121879		"Breast cancer, somatic, 114480 (3); CLOVE syndrome, somatic, 612918 (3); Colorectal cancer, somatic, 114500 (3); Cowden syndrome 5, 615108 (3); Gastric cancer, somatic, 613659 (3); Hepatocellular carcinoma, somatic, 114550 (3); Keratosis, seborrheic, somatic, 182000 (3); Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic, 602501 (3); Nevus, epidermal, somatic, 162900 (3); Nonsmall cell lung cancer, somatic, 211980 (3); Ovarian cancer, somatic, 167000 (3)"	Pik3ca (MGI:1206581)			
chr3	179239748	179267049	3q26.3-q27.1	3q26.32		605222	KCNMB3	"Potassium large conductance calcium-activated channel, subfamily M, beta member 3"	KCNMB3	27094	ENSG00000171121			Kcnmb3 (MGI:3612244)			
chr3	179396087	179451582	3q26.3	3q26.33		610863	"GNB4, CMTD1F"	"Guanine nucleotide-binding protein, beta-4"	GNB4	59345	ENSG00000114450		"Charcot-Marie-Tooth disease, dominant intermediate F, 615185 (3), Autosomal dominant"	Gnb4 (MGI:104581)			
chr3	179562879	179588404	3q26.3	3q26.33		604958	"ACTL6A, BAF53, BAF53A"	Actin-like 6A	ACTL6A	86	ENSG00000136518			Actl6a (MGI:1861453)			
chr3	179588464	179604645	3q26.3	3q26.33		611852	MRPL47	Mitochondrial ribosomal protein L47	MRPL47	57129	ENSG00000136522			Mrpl47 (MGI:1921850)			
chr3	179653144	179789400	3q26.2-q26.3	3q26.33		603591	"USP13, ISOT3"	Ubiquitin-specific protease-13	USP13	8975	ENSG00000058056			Usp13 (MGI:1919857)			
chr3	179794957	180037052	3q26.2-q27	3q26.33		611058	"PEX5L, PEX5R, PXR2B"	Peroxisome biogenesis factor 5-like	PEX5L	51555	ENSG00000114757			Pex5l (MGI:1916672)			
chr3	180614007	180679494	3q26.33	3q26.33		613798	CCDC39	Coiled-coil domain-containing protein 39	CCDC39	339829	ENSG00000284862		"Ciliary dyskinesia, primary, 14, 613807 (3)"	Ccdc39 (MGI:1289263)			
chr3	180912445	180982752	3q28	3q26.33		600819	FXR1	"Fragile X mental retardation, autosomal homolog"	FXR1	8087	ENSG00000114416	pseudogene on 12q12		Fxr1 (MGI:104860)			
chr3	180983708	180989773	3q26.3	3q26.33		608977	"DNAJC19, TIM14"	"DnaJ (Hsp40) homolog, subfamily C, member 19 (translocase of inner mitochondrial membrane 14, yeast, homolog of)"	DNAJC19	131118	ENSG00000205981		"3-methylglutaconic aciduria, type V, 610198 (3), Autosomal recessive"	"Dnajc19-ps,Dnajc19 (MGI:1914963,MGI:3709029)"			
chr3	181056679	181742227	3q26.33	3q26.33		616338	"SOX2OT, NCRNA00043"	"SOX2 overlapping transcript, noncoding"	SOX2-OT	347689							
chr3	181711923	181714435	3q26.3-q27	3q26.33		184429	"SOX2, MCOPS3"	SRY (sex determining region Y)-box 2	SOX2	6657	ENSG00000181449		"Microphthalmia, syndromic 3, 206900 (3), Autosomal dominant; Optic nerve hypoplasia and abnormalities of the central nervous system, 206900 (3), Autosomal dominant"	Sox2 (MGI:98364)			
chr3	182793502	182923009	3q27	3q26.33		605869	"ATP11B, ATPIR"	"ATPase, class VI, type 11B"	ATP11B	23200	ENSG00000058063			Atp11b (MGI:1923545)			
chr3	182938157	182986363	3q26.3	3q26.33		605905	"DCUN1D1, RP42"	DCN1 domain-containing protein 1	DCUN1D1	54165	ENSG00000043093	previously mapped to 6q16		Dcun1d1 (MGI:2150386)			
chr3	183000000	188200000	3q27			605552	"AOMS1, SYNX"	Abdominal obesity-metabolic syndrome QTL1		65076		epistatic gene on 17p12	"Abdominal obesity-metabolic syndrome 1, 605552 (2), Autosomal dominant"				
chr3	183000000	192600000	3q27-q28			605229	SPG14	"Spastic paraplegia 14, autosomal recessive"	SPG14	57309			"Spastic paraplegia 14, autosomal recessive, 605229 (2), Autosomal recessive"				
chr3	183015217	183099586	3q25-q27	3q27.1		609010	"MCCC1, MCCA"	3-Methylcrotonyl-CoA carboxylase 1	MCCC1	56922	ENSG00000078070		"3-Methylcrotonyl-CoA carboxylase 1 deficiency, 210200 (3), Autosomal recessive"	Mccc1 (MGI:1919289)			
chr3	183122214	183162878	3q26.3-q27	3q27.1		605883	DCLAMP	"Lysosome-associated membrane glycoprotein, dendritic cell-specific"	LAMP3	27074	ENSG00000078081			Lamp3 (MGI:2441659)			
chr3	183253206	183273390	3q27.1	3q27.1		615333	B3GNT5	"Beta-1,3-N-acetylglucosaminyltransferase 5"	B3GNT5	84002	ENSG00000176597			B3gnt5 (MGI:2137302)			
chr3	183487527	183555711	3q27.3	3q27.1		614214	"KLHL6, FLJ00029"	Kelch-like 6	KLHL6	89857	ENSG00000172578			Klhl6 (MGI:2686922)			
chr3	183635618	183684518	3q27.1	3q27.1		611295	"KLHL24, KRIP6, EBSSH"	Kelch-like 24	KLHL24	54800	ENSG00000114796		"Epidermolysis bullosa simplex, generalized, with scarring and hair loss, 617294 (3), Autosomal dominant"	Klhl24 (MGI:1923035)			
chr3	183697803	183812624	3q27.1	3q27.1		613373	"YEATS2, KIAA1197"	YEATS domain-containing protein 2	YEATS2	55689	ENSG00000163872			Yeats2 (MGI:2447762)			
chr3	183815875	183825604	3q27	3q27.1		610593	"MAPO6D1, SL21"	MAP6 domain-containing protein 1	MAP6D1	79929	ENSG00000180834			Map6d1 (MGI:3607784)			
chr3	183826487	183884907	3q27	3q27.1		607858	PARL	Presenilin-associated rhomboid-like protein	PARL	55486	ENSG00000175193			Parl (MGI:1277152)			
chr3	183919933	184018009	3q27	3q27.1		605251	"ABCC5, MRP5, MOATC"	"ATP-binding cassette, subfamily C, member 5"	ABCC5	10057	ENSG00000114770			Abcc5 (MGI:1351644)			
chr3	184031543	184039368	3q27	3q27.1		610122	HTR3D	"5-hydroxytryptamine receptor 3, subunit D"	HTR3D	200909	ENSG00000186090						
chr3	184053046	184060672	3q27	3q27.1		610121	HTR3C	5-hydroxytryptamine receptor 3C	HTR3C	170572	ENSG00000178084						
chr3	184097063	184106994	3q27	3q27.1		610123	HTR3E	"5-hydroxytryptamine receptor 3, subunit E"	HTR3E	285242	ENSG00000186038						
chr3	184135021	184145310	3q27	3q27.1		603945	"EIF2B5, LVWM, CACH, CLE"	"Eukaryotic translation initiation factor 2B, subunit 5"	EIF2B5	8893	ENSG00000145191		"Leukoencephalopathy with vanishing white matter, 603896 (3), Autosomal recessive; Ovarioleukodystrophy, 603896 (3), Autosomal recessive"	Eif2b5 (MGI:2446176)			
chr3	184155310	184173613	3q27	3q27.1		601368	"DVL3, DRS3"	Dishevelled 3 (homologous to Drosophila dsh)	DVL3	1857	ENSG00000161202		"Robinow syndrome, autosomal dominant 3, 616894 (3), Autosomal dominant"	Dvl3 (MGI:108100)			
chr3	184174845	184184090	3q28	3q27.1		601024	"AP2M1, CLAPM1"	"Adaptor-related protein complex 2, mu 1 subunit"	AP2M1	1173	ENSG00000161203			Ap2m1 (MGI:1298405)			
chr3	184241404	184241488	3q27.1	3q27.1		611620	"MIR1224, MIRN1224"	Micro RNA 1224	MIR1224	100187716							
chr3	184242328	184258300	3q27	3q27.1		608750	"ALG3, NOT56L, CDGS4, CDG1D"	"Alg3, S. cerevisiae, homolog of"	ALG3	10195	ENSG00000214160		"Congenital disorder of glycosylation, type Id, 601110 (3), Autosomal recessive"	Alg3 (MGI:1098592)			
chr3	184259214	184261462	3q27.1	3q27.1		608721	"CAMK2N2, CAMKIIN"	Calcium/calmodulin-dependent protein kinase II inhibitor 2	CAMK2N2	94032	ENSG00000163888			Camk2n2 (MGI:1920297)			
chr3	184276010	184293030	3q27.1	3q27.1		610145	"ECE2, KIAA0604"	Endothelin-converting enzyme 2	ECE2	9718	ENSG00000145194			Ece2 (MGI:1101356)			
chr3	184299097	184309053	3q27.1	3q27.1		606223	"PSMD2, S2, TRAP2"	"Proteasome 26S subunit, non-APTase, 2"	PSMD2	5708	ENSG00000175166			Psmd2 (MGI:1096584)			
chr3	184314494	184335357	3q27	3q27.1		600495	"EIF4G1, EIF4G, PARK18"	"Eukaryotic translation initiation factor 4 gamma, 1"	EIF4G1	1981	ENSG00000114867	amplified in squamous cell lung cancer	"{Parkinson disease 18}, 614251 (3), Autosomal dominant"	Eif4g1 (MGI:2384784)			
chr3	184346184	184361650	3q26	3q27.1		600570	"CLCN2, EGMA, ECA2, EGI11, EJM8, LKPAT"	Chloride channel-2	CLCN2	1181	ENSG00000114859		"{Epilepsy, idiopathic generalized, susceptibility to, 11}, 607628 (3), Autosomal dominant; {Epilepsy, juvenile absence, susceptibility to, 2}, 607628 (3), Autosomal dominant; {Epilepsy, juvenile myoclonic, susceptibility to, 8}, 607628 (3), Autosomal dominant; Leukoencephalopathy with ataxia, 615651 (3), Autosomal recessive"	Clcn2 (MGI:105061)			
chr3	184361709	184368594	3q28	3q27.1		606023	"POLR2H, RPB8"	"Polymerase II, RNA, subunit H"	POLR2H	5437	ENSG00000163882			Polr2h (MGI:2384309)			
chr3	184371934	184379687	3q26.3-q27	3q27.1		600044	"THPO, MGDF, MPLLG, TPO, THCYT1"	Thrombopoietin (megakaryocyte growth and development factor)	THPO	7066	ENSG00000090534		"Thrombocythemia 1, 187950 (3), Autosomal dominant"	Thpo (MGI:101875)			
chr3	184380072	184389834	3q27	3q27.1		603475	CHRD	Chordin	CHRD	8646	ENSG00000090539	"near THPO, CLCN2, EIF4G1"		Chrd (MGI:1313268)			
chr3	184561798	184582407	3q21-qter	3q27.1		601839	"EPHB3, ETK2"	EPH-like tyrosine kinase-2	EPHB3	2049	ENSG00000182580			Ephb3 (MGI:104770)			
chr3	184710366	184712047	3q13	3q27.1		609267	MAGEF1	"Melanoma antigen, family F, 1"	MAGEF1	64110	ENSG00000177383						
chr3	185190623	185254097	3q27	3q27.2		607037	"EHHADH, PBFE, LBFP, FRTS3"	"Enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase"	EHHADH	1962	ENSG00000113790	mutation identified in 1 family	"?Fanconi renotubular syndrome 3, 615605 (3), Autosomal dominant"	Ehhadh (MGI:1277964)			
chr3	185282937	185489093	3q27	3q27.2		604915	"MAP3K13, LZK"	Mitogen-activated protein kinase kinase kinase 13 (leucine zipper-bearing kinase)	MAP3K13	9175	ENSG00000073803			Map3k13 (MGI:2444243)			
chr3	185507044	185552660	3q27-q28	3q27.2		607365	"LIPH, LAH2, ARWH2, HYPT7"	Lipase H	LIPH	200879	ENSG00000163898		"Hypotrichosis 7, 604379 (3), Autosomal recessive; Woolly hair, autosomal recessive 2 with or without hypotrichosis, 604379 (3), Autosomal recessive"	Liph (MGI:2388029)			
chr3	185586242	185631100	3q27	3q27.2		608261	"SENP2, SMT3IP2, AXAM2, KIAA1331"	"Sentrin-specific protease family, member 2"	SENP2	59343	ENSG00000163904			Senp2 (MGI:1923076)			
chr3	185643130	185825055	3q28	3q27.2		608289	"IGF2BP2, IMP2"	Insulin-like growth factor 2 mRNA-binding protein 2	IGF2BP2	10644	ENSG00000073792		"{Diabetes mellitus, noninsulin-dependent, susceptibility to}, 125853 (3), Autosomal dominant"	Igf2bp2 (MGI:1890358)			
chr3	185914567	185938135	3q26.2-q27	3q27.2		602719	"TRA2B, SFRS10"	"Splicing factor, arginine/serine-rich, 10 (transformer 2, drosophila, homolog of, beta)"	TRA2B	6434	ENSG00000136527			Tra2b (MGI:106016)			
chr3	186046316	186109111	3q28	3q27.2		601600	"ETV5, ERM"	ets variant gene 5 (ets-related molecule)	ETV5	2119	ENSG00000244405			Etv5 (MGI:1096867)			
chr3	186147200	186362233	3q27-q28	3q27.2-q27.3		601854	"DGKG, DAGK3"	"Diacylglycerol kinase, gamma, 90-kD"	DGKG	1608	ENSG00000058866			Dgkg (MGI:105060)			
chr3	186538438	186544450	3q27	3q27.3		123730	"CRYGS, CRYG8, CTRCT20"	"Crystallin, gamma S"	CRYGS	1427	ENSG00000213139		"Cataract 20, multiple types, 116100 (3), Autosomal dominant"	Crygs (MGI:1298216)			
chr3	186570675	186585799	3q27.3	3q27.3		611341	"DNAJB11, HEDJ, DJ9, ABBP2"	"DNAJ/HSP40 homolog, subfamily B, member 11"	DNAJB11	51726	ENSG00000090520			Dnajb11 (MGI:1915088)			
chr3	186612922	186621317	3q27	3q27.3		138680	"AHSG, APMR1"	Alpha-2HS-glycoprotein	AHSG	197	ENSG00000145192	mutation identified in 1 APMR1 family	"?Alopecia-mental retardation syndrome 1, 203650 (3), Autosomal recessive"	Ahsg (MGI:107189)			
chr3	186635827	186653007	3q27	3q27.3		605954	FETUB	Fetuin B	FETUB	26998	ENSG00000090512			Fetub (MGI:1890221)			
chr3	186665951	186678239	3q27	3q27.3		142640	"HRG, THPH11"	Histidine-rich glycoprotein	HRG	3273	ENSG00000113905		"Thrombophilia due to HRG deficiency, 613116 (3), Autosomal dominant; Thrombophilia due to elevated HRG, 613116 (1), Autosomal dominant"				
chr3	186717308	186744409	3q27	3q27.3		612358	"KNG1, KNG"	Kininogen 1	KNG1	3827	ENSG00000113889		"[High molecular weight kininogen deficiency], 228960 (3), Autosomal recessive; [Kininogen deficiency], 228960 (3), Autosomal recessive"	"Kng2,Kng1 (MGI:1097705,MGI:3027157)"			
chr3	186783571	186789896	3q28	3q27.3		601102	EIF4A2	"Eukaryotic translation initiation factor-4A, isoform 2"	EIF4A2	1974	ENSG00000156976	previously 18p11.2 by FISH		Eif4a2 (MGI:106906)			
chr3	186786674	186786851	3q27.3	3q27.3		611334	SNORA81	"Small nucleolar RNA, H/ACA box, 81"	SNORA81	677847		in intron 3 of EIF2A					
chr3	186787298	186787432	3q27.3	3q27.3		180647	"SNORA63, RNU107, RNE3"	"Small nucleolar RNA, H/ACA box, 63"	SNORA63	6043							
chr3	186789891	186806694	3q27	3q27.3		102577	RFC4	"Replication factor C4, 37kD (activator 1, 37kD)"	RFC4	5984	ENSG00000163918			Rfc4 (MGI:2146571)			
chr3	186842673	186858462	3q27	3q27.3		605441	"ADIPOQ, APM1, GBP28, ADIPQTL1"	"Adipocyte-, C1q-, and collagen domain-containing"	ADIPOQ	9370	ENSG00000181092		"Adiponectin deficiency, 612556 (3)"	Adipoq (MGI:106675)			
chr3	186930525	187078552	3q21-q28	3q27.3		109675	SIAT1	"Sialyltransferase-1 (beta-galactoside alpha-2,6-sialyltransferase)"	ST6GAL1	6480	ENSG00000073849			St6gal1 (MGI:108470)			
chr3	187120947	187139522	3q27	3q27.3		607547	RPL39L	Ribosomal protein L39-like	RPL39L	116832	ENSG00000163923						
chr3	187197485	187201464	3q27.3	3q27.3		609137	RTP1	Receptor-transporting protein 1	RTP1	132112	ENSG00000175077			Rtp1 (MGI:2685450)			
chr3	187216084	187293528	3q27-q28	3q27.3		600521	"MASP1, CRARF, 3MC1"	Mannan-binding lectin serine protease-1 (C4/C2 activating component of Ra-reactive factor)	MASP1	5648	ENSG00000127241		"3MC syndrome 1, 257920 (3), Autosomal recessive"				
chr3	187368379	187371583	3q27	3q27.3		609350	RTP4	Receptor-transporting protein 4	RTP4	64108	ENSG00000136514			Rtp4 (MGI:1915025)			
chr3	187668905	187670412	3q28	3q27.3		182450	SST	Somatostatin	SST	6750	ENSG00000157005			Sst (MGI:98326)			
chr3	187698258	187715624	3q27.3	3q27.3		609138	RTP2	Receptor-transporting protein 2	RTP2	344892	ENSG00000198471			Rtp2 (MGI:2685451)			
chr3	187721376	187745724	3q27	3q27.3		109565	BCL6	B-cell CLL/lymphoma-6	BCL6	604	ENSG00000113916		"Lymphoma, B-cell, 109565 (2)"	Bcl6 (MGI:107187)			
chr3	188152151	188890670	3q28	3q27-q28		600700	LPP	Lipoma-preferred-partner gene	LPP	4026	ENSG00000145012	fused with HMGIC in lipoma; fused with MLL in leukemia	"Leukemia, acute myeloid, 601626 (3), Autosomal dominant; Lipoma (3)"	Lpp (MGI:2441849)			
chr3	188200000	192600000	3q28			612009	CELIAC11	"Celiac disease, susceptibility to, 11"		100188873		associated with rs1464510	"{Celiac disease, susceptibility to, 11}, 612009 (2)"				
chr3	188200000	192600000	3q28			614210	LNCR5	Lung cancer susceptibility 5		100682395		associated with rs4488809	"{Lung cancer susceptibility 5}, 614210 (2)"				
chr3	188688780	188688865	3q28	3q28		612154	"MIR28, MIRN28"	Micro RNA 28	MIR28	407020							
chr3	189596745	189897278	3q27	3q28		603273	"TP63, TP73L, KET, EEC3, SHFM4, LMS, RHS, OFC8"	Tumor protein p63 (tumor protein p73-like)	TP63	8626	ENSG00000073282		"ADULT syndrome, 103285 (3), Autosomal dominant; Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3, 604292 (3), Autosomal dominant; Hay-Wells syndrome, 106260 (3), Autosomal dominant; Limb-mammary syndrome, 603543 (3), Autosomal dominant; Orofacial cleft 8, 129400 (3), Autosomal dominant; Rapp-Hodgkin syndrome, 129400 (3), Autosomal dominant; Split-hand/foot malformation 4, 605289 (3), Autosomal dominant"	Trp63 (MGI:1330810)			
chr3	189956727	190122436	3q29	3q28		610341	"P3H2, LEPREL1, MCVD"	Prolyl 3-hydroxylase 2	P3H2	55214	ENSG00000090530		"Myopia, high, with cataract and vitreoretinal degeneration, 614292 (3), Autosomal recessive"	P3h2 (MGI:2146663)			
chr3	190305700	190322445	3q28-q29	3q28		603718	"CLDN1, SEMP1, ILVASC"	Claudin 1	CLDN1	9076	ENSG00000163347		"Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis, 607626 (3), Autosomal recessive"	Cldn1 (MGI:1276109)			
chr3	190387871	190412142	3q27	3q28		603959	"CLDN16, PCLN1, HOMG3"	Claudin 16 (paracellin 1)	CLDN16	10686	ENSG00000113946		"Hypomagnesemia 3, renal, 248250 (3), Autosomal recessive"	Cldn16 (MGI:2148742)			
chr3	190428654	190449875	3q28	3q28		614786	TMEM207	Transmembrane protein 207	TMEM207	131920	ENSG00000198398			Tmem207 (MGI:2685386)			
chr3	190514050	190657196	3q28	3q28		602626	IL1RAP	Interleukin 1 receptor accessory protein	IL1RAP	3556	ENSG00000196083			Il1rap (MGI:104975)			
chr3	190843270	190864199	3q28	3q28		614448	"GMNC, GEMC1"	Geminin coiled-coil domain-containing protein	GMNC	647309	ENSG00000205835			Gmnc (MGI:2685452)			
chr3	191199240	191265614	3q26	3q28		610280	OSTN	Osteocrin	OSTN	344901	ENSG00000188729			Ostn (MGI:2677164)			
chr3	191329081	191398669	3q28	3q28		611051	"CCDC50, C3orf6, DFNA44"	Coiled-coil domain-containing protein 50	CCDC50	152137	ENSG00000152492	mutation identified in 1 DFNA44 family	"?Deafness, autosomal dominant 44, 607453 (3), Autosomal dominant"				
chr3	191461162	191461455	3q28	3q28		615701	"PYDC2, POP2"	Pyrin domain-containing protein 2	PYDC2	152138	ENSG00000253548						
chr3	192139392	192727598	3q28	3q28-q29		601513	"FGF12, FHF1, EIEE47"	Fibroblast growth factor-12	FGF12	2257	ENSG00000114279		"Epileptic encephalopathy, early infantile, 47, 617166 (3), Autosomal dominant"	Fgf12 (MGI:109183)			
chr3	192600000	198295559	3q29			609425	"DEL3q29, MICRODEL3q29"	Chromosome 3q29 microdeletion syndrome				contiguous gene deletion syndrome	"Chromosome 3q29 microdeletion syndrome, 609425 (4), Isolated cases"				
chr3	192600000	198295559	3q29			611936	"DUP3q29, MICRODUP3q29"	Chromosome 3q29 microduplication syndrome				contiguous gene duplication syndrome	"Chromosome 3q29 microduplication syndrome, 611936 (4), Autosomal dominant"				
chr3	193241127	193281638	3q28-q29	3q29		606487	HRASLS	HRAS-like suppressor	HRASLS	57110	ENSG00000127252			Hrasls (MGI:1351473)			
chr3	193398966	193593113	3q29	3q29		609556	ATP13A4	"ATPase, type 13A4"	ATP13A4	84239	ENSG00000127249			Atp13a4 (MGI:1924456)			
chr3	193593143	193697810	3q28-q29	3q29		605290	"OPA1, NTG, NPG, BERHS, MTDPS14"	Optic atrophy 1 gene	OPA1	4976	ENSG00000198836	mutation identified in 1 MTDPS14 family	"Behr syndrome, 210000 (3), Autosomal recessive; {Glaucoma, normal tension, susceptibility to}, 606657 (3); ?Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type), 616896 (3); Optic atrophy 1, 165500 (3), Autosomal dominant; Optic atrophy plus syndrome, 125250 (3), Autosomal dominant"	Opa1 (MGI:1921393)			
chr3	194136141	194138611	3q28-q29	3q29		139605	"HES1, HRY"	"Hairy and enhancer of split, Drosophila, homolog of"	HES1	3280	ENSG00000114315			Hes1 (MGI:104853)			
chr3	194339764	194351386	3q29	3q29		603104	CPN2	"Carboxypeptidase N, polypeptide 2, 83-KD"	CPN2	1370	ENSG00000178772	conflicting assignment to chr.8		Cpn2 (MGI:1919006)			
chr3	194394820	194399265	3q29	3q29		173511	GP5	"Glycoprotein V, platelet"	GP5	2814	ENSG00000178732			Gp5 (MGI:1096363)			
chr3	194402673	194487005	3q26.32	3q29		610232	"ATP13A3, AFURS1"	"ATPase, type 13A3"	ATP13A3	79572	ENSG00000133657			Atp13a3 (MGI:2685387)			
chr3	194640787	194672476	3q29	3q29		610780	LSG1	"Large subunit GTPase 1, S. cerevisiae, homolog of"	LSG1	55341	ENSG00000041802			Lsg1 (MGI:107236)			
chr3	195066969	195271165	3q29	3q29		614552	"XXYLT1, C3orf21"	Xyloside xylosyltransferase 1	XXYLT1	152002	ENSG00000173950			Xxylt1 (MGI:2146443)			
chr3	195274735	195443175	3q29	3q29		607766	"CENTB2, KIAA0041, ACAP2"	"Centaurin, beta-2"	ACAP2	23527	ENSG00000114331			Acap2 (MGI:1925868)			
chr3	195514421	195543400	3q29	3q29		601792	"PPP1R2, IPP2"	"Protein phosphatase-1, regulatory (inhibitor) subunit 2"	PPP1R2	5504	ENSG00000184203	pseudogenes on chr. 5 and 6		Ppp1r2 (MGI:1914099)			
chr3	195568701	195584204	3q26.2-qter	3q29		107740	APOD	Apolipoprotein D	APOD	347	ENSG00000189058			Apod (MGI:88056)			
chr3	195699400	195699496	3q29	3q29		614538	MIR570	Micro RNA 570	MIR570	693155							
chr3	195720881	195733552	3q29	3q29		610360	MUC20	"Mucin 20, cell surface-associated"	MUC20	200958	ENSG00000176945			Muc20 (MGI:2385039)			
chr3	195746764	195811972	3q29	3q29		158372	MUC4	"Mucin 4, tracheobronchial"	MUC4	4585	ENSG00000145113						
chr3	195863363	195909008	3q29	3q29		606994	"TNK2, ACK, ACK1"	"Tyrosine kinase, non-receptor, 2"	TNK2	10188	ENSG00000061938			Tnk2 (MGI:1858308)			
chr3	196018693	196082160	3q29	3q29		190010	"TFRC, TFR, CD71, IMD46"	Transferrin receptor	TFRC	7037	ENSG00000072274		"Immunodeficiency 46, 616740 (3), Autosomal recessive"	Tfrc (MGI:98822)			
chr3	196216511	196233429	3q29	3q29		612084	OSTA	"Organic solute transporter, alpha"	SLC51A	200931	ENSG00000163959			Slc51a (MGI:2146634)			
chr3	196237744	196287751	3q29	3q29		123695	"PCYT1A, CTPCT, PCYT1, SMDCRD"	"Phosphate cytidylyltransferase 1, choline, alpha isoform"	PCYT1A	5130	ENSG00000161217		"Spondylometaphyseal dysplasia with cone-rod dystrophy, 608940 (3), Autosomal recessive"	Pcyt1a (MGI:88557)			
chr3	196291218	196318293	3q29	3q29		617353	"TCTEX1D2, SRTD17"	TCTEX1 domain-containing protein 2	TCTEX1D2	255758	ENSG00000213123		"Short-rib thoracic dysplasia 17 with or without polydactyly, 617405 (3), Autosomal recessive"	Tctex1d2 (MGI:1913311)			
chr3	196347658	196454322	3q29	3q29		616379	"UBXN7, KIAA0794"	UBX domain protein 7	UBXN7	26043	ENSG00000163960			Ubxn7 (MGI:2146388)			
chr3	196468782	196503767	3q29	3q29		612688	RNF168	RING finger protein 168	RNF168	165918	ENSG00000163961		"RIDDLE syndrome, 611943 (3), Autosomal recessive"	Rnf168 (MGI:1917488)			
chr3	196554176	196568673	3q29	3q29		615110	WDR53	WD repeat-containing protein 53	WDR53	348793	ENSG00000185798			Wdr53 (MGI:1916230)			
chr3	196568853	196589058	3q29	3q29		609112	"FBXO45, FBX45"	F-box only protein 45	FBXO45	200933	ENSG00000174013			Fbxo45 (MGI:2447775)			
chr3	196639695	196662003	3q29	3q29		615322	"NRROS, LRRC33"	Negative regulator of oxygen species	NRROS	375387	ENSG00000174004			Nrros (MGI:2445095)			
chr3	196706272	196712293	3q29	3q29		615586	"CEP19, C3orf34, MOSPGF"	"Centrosomal protein, 19kD"	CEP19	84984	ENSG00000174007	mutation identified in 1 family	"Morbid obesity and spermatogenic failure, 615703 (3), Autosomal recessive"	Cep19 (MGI:1914244)			
chr3	196712373	196736006	3q29	3q29		610276	PIGX	"Phosphatidylinositol glycan, class X"	PIGX	54965	ENSG00000163964			Pigx (MGI:1919334)			
chr3	196739856	196832646	3q29	3q29		605022	"PAK2, PAK65"	p21-activated kinase 2	PAK2	5062	ENSG00000180370	deleted in 3q29 microdeletion syndrome		Pak2 (MGI:1339984)			
chr3	196867855	196934713	3q29	3q29		612845	SENP5	"Sentrin-specific protease family, member 5"	SENP5	205564	ENSG00000119231			Senp5 (MGI:2443596)			
chr3	196932728	196942592	3q29	3q29		605133	"NCBP2, CBP20, NIP1"	Nuclear CAP-binding protein 2	NCBP2	22916	ENSG00000114503			Ncbp2 (MGI:1915342)			
chr3	196946342	196969410	3q29	3q29		611671	"PIGZ, SMP3"	"Phosphatidylinositol glycan, class Z"	PIGZ	80235	ENSG00000119227			Pigz (MGI:2443822)			
chr3	197001739	197029815	3q29	3q29		155750	"MFI2, MAP97"	Melanoma-associated antigen p97	MELTF	4241	ENSG00000163975			Meltf (MGI:1353421)			
chr3	197042559	197299271	3q29	3q29		601014	DLG1	"Discs, large, Drosophila, homolog of, 1"	DLG1	1739	ENSG00000075711	deleted in 3q29 microdeletion syndrome		Dlg1 (MGI:107231)			
chr3	197509782	197573322	3q29	3q29		603063	"BDH1, BDH"	3-hydroxybutyrate dehydrogenase 1	BDH1	622	ENSG00000161267			Bdh1 (MGI:1919161)			
chr3	197668866	197749726	3q29	3q29		613516	"RUBCN, RUBICON, KIAA0226, SCAR15"	"RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein"	RUBCN	9711	ENSG00000145016	mutation identified in 1 family	"?Spinocerebellar ataxia, autosomal recessive 15, 615705 (3), Autosomal recessive"	Rubcn (MGI:1915160)			
chr3	197749552	197784445	3q29	3q29		616933	"FYTTD1, UIF"	Forty-two-three domain-containing protein 1	FYTTD1	84248	ENSG00000122068			Fyttd1 (MGI:1917955)			
chr3	197889074	197960110	3q29	3q29		612477	IQCG	IQ motif-containing protein G	IQCG	84223	ENSG00000114473			Iqcg (MGI:1916957)			
chr3	197950189	197955850	3q29-qter	3q29		180468	"RPL35A, DBA5"	Ribosomal protein L35A	RPL35A	6165	ENSG00000182899	previous assignment to chr.18 in error	"Diamond-Blackfan anemia 5, 612528 (3), Autosomal dominant"	Rpl35a (MGI:1928894)			
chr3	197960199	198043719	3q29	3q29		609380	LMLN	Leishmanolysin-like	LMLN	89782	ENSG00000185621			Lmln (MGI:2444736)			
chr4	0	11300000	4p16			600593	"CRSA, CRS3"	"Craniosynostosis, Adelaide type"		7885			"Craniosynostosis, Adelaide type, 600593 (2), ?Autosomal dominant"				
chr4	0	182300000	4p16-q34			603783	INTLQ1	Intelligence quantitative trait locus 1		100462721		"associated with D4S2943, MSX1, and D4S1607"	"{Intelligence QTL1}, 603783 (2)"				
chr4	0	4500000	4p16.3			609456	MDCMP	"Muscular dystrophy, congenital, merosin-positive"		619409		max lod at D4S432	"Muscular dystrophy, congenital, merosin-positive, 609456 (2), Autosomal recessive"				
chr4	0	50000000	4p			603663	MHW1	Mental health wellness 1		10386		at D4S2949	"{Mental health wellness-1}, 603663 (2)"				
chr4	0	35800000	4p16-p15			611863	MNDEC	Microtia with nasolacrimal duct imperforation and eye coloboma		100188855		copy number variant (CNV) association	Microtia with nasolacrimal duct imperforation and eye coloboma (1)				
chr4	0	11300000	4p16			611637	"PLSA1, PLSA"	"Primary lateral sclerosis, adult, 1"		100240702		max lod at D4S2936	"Primary lateral sclerosis, adult, 1, 611637 (2), Autosomal dominant"				
chr4	0	27700000	4p16-p15.2			605480	SLEB3	"Systemic lupus erythematosus, susceptibility to, 3"	SLEB3	64695			"{Systemic lupus erythematosus, susceptibility to, 3}, 605480 (2)"				
chr4	0	35800000	4p16-p15			612335	SPG38	"Spastic paraplegia 38, autosomal dominant"	SPG38	100049707		between D4S432 and D4S1599	"Spastic paraplegia 38, autosomal dominant, 612335 (2), Autosomal dominant"				
chr4	0	4500000	4p16.3			194190	WHS	Wolf-Hirschhorn syndrome				contiguous gene syndrome; critical region 200kb region 1.9Mb from telomere	"Wolf-Hirschhorn syndrome, 194190 (4), Isolated cases"				
chr4	337778	384863	4p16.3	4p16.3		194648	"ZNF141, D4S90, PAPA6"	Zinc finger protein-141 (clone pHZ-44)	ZNF141	7700	ENSG00000131127	1 family identified with mutation	"?Polydactyly, postaxial, type A6, 615226 (3), Autosomal recessive"				
chr4	499199	540195	4p16.3	4p16.3		616918	"PIGG, GPI7, MRT53"	Phosphatidylinositol glycan anchor biosynthesis class G protein	PIGG	54872	ENSG00000174227		"Mental retardation, autosomal recessive 53, 616917 (3), Autosomal recessive"	Pigg (MGI:3576484)			
chr4	587324	670891	4p16.3	4p16.3		180072	"PDE6B, PDEB, RP40, CSNBAD2"	"Phosphodiesterase-6B, cGMP-specific, rod, beta"	PDE6B	5158	ENSG00000133256		"Night blindness, congenital stationary, autosomal dominant 2, 163500 (3), Autosomal dominant; Retinitis pigmentosa-40, 613801 (3), Autosomal recessive"	Pde6b (MGI:97525)			
chr4	672435	674337	4p16.3	4p16.3		601519	"ATP5I, ATP5K"	"ATP synthase, H+ transporting, mitochondrial FO complex, subunit E"	ATP5ME	521	ENSG00000169020						
chr4	674198	682032	4p16.3	4p16.3		160782	MYL5	"Myosin, light polypeptide-5, regulatory"	MYL5	4636	ENSG00000215375						
chr4	705740	770979	4p16.3	4p16.3		617543	"PCGF3, RNF3, RNF3A"	Polycomb group RING finger protein 3	PCGF3	10336	ENSG00000185619			Pcgf3 (MGI:1916837)			
chr4	784956	826156	4p16.3	4p16.3		605032	"CPLX1, CPX1"	Complexin 1	CPLX1	10815	ENSG00000168993			Cplx1 (MGI:104727)			
chr4	849274	932389	4p16	4p16.3		602052	GAK	Cyclin G associated kinase	GAK	2580	ENSG00000178950			Gak (MGI:2442153)			
chr4	932386	958655	4p16.3	4p16.3		616660	TMEM175	Transmembrane protein 175	TMEM175	84286	ENSG00000127419			Tmem175 (MGI:1919642)			
chr4	958883	973559	4p16.3	4p16.3		601207	"DGKQ, DAGK4"	"Diacylglycerol kinase, theta, 110kD"	DGKQ	1609	ENSG00000145214			Dgkq (MGI:102918)			
chr4	979072	993439	4p16.3	4p16.3		610130	"SLC26A1, SAT1, CAON"	"Solute carrier family 26 (sulfate transporter), member 1"	SLC26A1	10861	ENSG00000145217	mutation identified in 1 CAON patient	"?Nephrolithiasis, calcium oxalate, 167030 (3), Autosomal recessive"	Slc26a1 (MGI:2385894)			
chr4	986996	1004556	4p16.3	4p16.3		252800	"IDUA, IDA"	"Iduronidase, alpha-L-"	IDUA	3425	ENSG00000127415		"Mucopolysaccharidosis Ih, 607014 (3), Autosomal recessive; Mucopolysaccharidosis Ih/s, 607015 (3), Autosomal recessive; Mucopolysaccharidosis Is, 607016 (3), Autosomal recessive"	Idua (MGI:96418)			
chr4	1009929	1026897	4p16	4p16.3		605830	FGFRL1	Fibroblast growth factor receptor-like 1	FGFRL1	53834	ENSG00000127418			Fgfrl1 (MGI:2150920)			
chr4	1056247	1113793	4p16.3	4p16.3		612041	"RNF212, ZHP3"	Ring finger protein 212	RNF212	285498	ENSG00000178222		"Recombination rate QTL 1, 612042 (3)"	Rnf212 (MGI:3645767)			
chr4	1166931	1208961	4p16.3	4p16.3		605918	SPON2	Spondin 2	SPON2	10417	ENSG00000159674			Spon2 (MGI:1923724)			
chr4	1211439	1253918	4p16	4p16.3		602618	"CTBP1, HADDTS"	C-terminal binding protein 1	CTBP1	1487	ENSG00000159692		"Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome, 617915 (3)"	Ctbp1 (MGI:1201685)			
chr4	1289850	1340147	4p16.3	4p16.3		606801	"MAEA, EMP"	Macrophage erythroblast attacher	MAEA	10296	ENSG00000090316			Maea (MGI:1891748)			
chr4	1341997	1388048	4p16.3	4p16.3		614632	"UVSSA, KIAA1530, UVSS3"	UV-stimulated scaffold protein A	UVSSA	57654	ENSG00000163945		"UV-sensitive syndrome 3, 614640 (3), Autosomal recessive"	Uvssa (MGI:1918351)			
chr4	1391551	1395993	4p16.3	4p16.3		610203	"CRIPAK, FLJ3443"	Cysteine-rich inhibitor of PAK1	CRIPAK	285464	ENSG00000163945						
chr4	1402931	1406441	4p16.3	4p16.3		617869	"NKX1-1, SAX2"	NK1 homeobox 1	NKX1-1	54729	ENSG00000235608						
chr4	1574054	1684312	4p16.3	4p16.3		617229	"FAM53A, DNTNP"	"Family with sequence similarity 53, member A"	FAM53A	152877	ENSG00000174137			Fam53a (MGI:1919225)			
chr4	1692730	1715875	4p16.3	4p16.3		602422	"SLBP, HBP"	Histone stem-loop binding protein	SLBP	7884	ENSG00000163950			Slbp (MGI:108402)			
chr4	1715951	1721372	4p16.3	4p16.3		615975	TMEM129	Transmembrane protein 129	TMEM129	92305	ENSG00000168936			Tmem129 (MGI:1915616)			
chr4	1721489	1745177	4p16.3	4p16.3		605303	TACC3	"Transforming, acidic, coiled-coil-containing protein 3"	TACC3	10460	ENSG00000013810			Tacc3 (MGI:1341163)			
chr4	1793298	1808871	4p16.3	4p16.3		134934	"FGFR3, ACH"	Fibroblast growth factor receptor-3	FGFR3	2261	ENSG00000068078		"Achondroplasia, 100800 (3), Autosomal dominant; Bladder cancer, somatic, 109800 (3); CATSHL syndrome, 610474 (3), Autosomal recessive, Autosomal dominant; Cervical cancer, somatic, 603956 (3); Colorectal cancer, somatic, 114500 (3); Crouzon syndrome with acanthosis nigricans, 612247 (3), Autosomal dominant; Hypochondroplasia, 146000 (3), Autosomal dominant; LADD syndrome, 149730 (3), Autosomal dominant; Muenke syndrome, 602849 (3), Autosomal dominant; Nevus, epidermal, somatic, 162900 (3); SADDAN, 616482 (3), Autosomal dominant; Spermatocytic seminoma, somatic, 273300 (3); Thanatophoric dysplasia, type I, 187600 (3), Autosomal dominant; Thanatophoric dysplasia, type II, 187601 (3), Autosomal dominant"	Fgfr3 (MGI:95524)			
chr4	1811478	1856246	4p16.3	4p16.3		604407	LETM1	Leucine zipper/EF-hand-containing transmembrane protein 1	LETM1	3954	ENSG00000168924			Letm1 (MGI:1932557)			
chr4	1871395	1982206	4p16.3	4p16.3		602952	"NSD2, WHSC1, MMSET"	Nuclear receptor-binding SET domain protein 2	NSD2	7468	ENSG00000109685			Nsd2 (MGI:1276574)			
chr4	1982713	2041913	4p16.3	4p16.3		606026	WHSC2	WHS candidate 2 gene	NELFA	7469	ENSG00000185049			Nelfa (MGI:1346098)			
chr4	2035609	2043969	4p16.3	4p16.3		614690	C4orf48	chromosome 4 open reading frame 48	C4orf48	401115	ENSG00000243449						
chr4	2059511	2069088	4p16.3	4p16.3		610647	"NAT8L, CML3, NACED"	N-acetyltransferase 8-like	NAT8L	339983	ENSG00000185818	mutation identified in 1 patient	"?N-acetylaspartate deficiency, 614063 (3), Autosomal recessive"	Nat8l (MGI:2447776)			
chr4	2071957	2242163	4p16.2	4p16.3		610887	POLN	"Polymerase, DNA, nu"	POLN	353497	ENSG00000130997						
chr4	2231835	2242163	4p16.3	4p16.3		613430	"HAUS3, DGT3, C4orf15"	"HAUS augmin-like complex, subunit 3"	HAUS3	79441	ENSG00000214367			Haus3 (MGI:2387633)			
chr4	2269584	2418697	4p16	4p16.3		614176	"ZFYVE28, LST2, KIAA1643"	Zinc finger FYVE domain-containing protein 28	ZFYVE28	57732	ENSG00000159733			Zfyve28 (MGI:2684992)			
chr4	2469067	2515858	4p16.3	4p16.3		602850	RNF4	RING finger protein-4	RNF4	6047	ENSG00000063978			Rnf4 (MGI:1201691)			
chr4	2741659	2756375	4p16.3	4p16.3		610669	"TNIP2, ABIN2, FLIP1"	TNFAIP3-interacting protein 2	TNIP2	79155	ENSG00000168884			Tnip2 (MGI:2386643)			
chr4	2793022	2841095	4p16.3	4p16.3		602104	"SH3BP2, CRPM"	SH3-domain binding protein 2	SH3BP2	6452	ENSG00000087266		"Cherubism, 118400 (3), Autosomal dominant"	Sh3bp2 (MGI:1346349)			
chr4	2843856	2930075	4p16.3	4p16.3		102680	ADD1	"Adducin-1, alpha"	ADD1	118	ENSG00000087274		"{Hypertension, essential, salt-sensitive}, 145500 (3), Multifactorial"	Add1 (MGI:87918)			
chr4	2930555	2934858	4p16.3	4p16.3		610977	"TETRAN, TPO1"	Tetracycline transporter-like protein	MFSD10	10227	ENSG00000109736			Mfsd10 (MGI:1915544)			
chr4	2937935	2963505	4p16.3	4p16.3		611526	"NOP14, NOL14, RES425"	"Nop14, S. cerevisiae, homolog of"	NOP14	8602	ENSG00000087269			Nop14 (MGI:1922666)			
chr4	2963503	3040759	4p16.3	4p16.3		137026	"GRK4, GPRK2L, GPRK4"	G protein-coupled receptor kinase 4	GRK4	2868	ENSG00000125388			Grk4 (MGI:95801)			
chr4	3074680	3243959	4p16.3	4p16.3		613004	"HTT, HD, IT15, LOMARS"	Huntingtin	HTT	3064	ENSG00000197386	distal to D4S10	"Huntington disease, 143100 (3), Autosomal dominant; Lopes-Maciel-Rodan syndrome, 617435 (3), Autosomal recessive"	Htt (MGI:96067)			
chr4	3292977	3439912	4p16.2	4p16.3		602512	RGS12	Regulator of G protein signaling 12	RGS12	6002	ENSG00000159788			Rgs12 (MGI:1918979)			
chr4	3441932	3449494	4p16	4p16.3		604552	"HGFAC, HGFA"	Hepatocyte growth factor activator	HGFAC	3083	ENSG00000109758			Hgfac (MGI:1859281)			
chr4	3463305	3501475	4p16.2	4p16.3		610285	"DOK7, C4orf25, CMS10"	Downstream of tyrosine kinase 7	DOK7	285489	ENSG00000175920	mutation identified in 1 FADS family	"?Fetal akinesia deformation sequence, 208150 (3), Autosomal recessive; Myasthenic syndrome, congenital, 10, 254300 (3), Autosomal recessive"	Dok7 (MGI:3584043)			
chr4	3503596	3532496	4p16.3	4p16.3		104225	"LRPAP1, A2MRAP, MYP23"	Low density lipoprotein-related protein-associated protein 1 (alpha-2-macroglobulin receptor-associated protein 1)	LRPAP1	4043	ENSG00000163956		"Myopia 23, autosomal recessive, 615431 (3), Autosomal recessive"	Lrpap1 (MGI:96829)			
chr4	3766568	3768525	4p16.1	4p16.3		104250	"ADRA2C, ADRA2L2"	"Adrenergic, alpha-2C-, receptor"	ADRA2C	152	ENSG00000184160	linked to D4S10	"{Congestive heart failure and beta-blocker response, modifier of} (3)"	Adra2c (MGI:87936)			
chr4	4188725	4226893	4p16.2	4p16.3		607806	OTOP1	Otopetrin 1	OTOP1	133060	ENSG00000163982			Otop1 (MGI:2388363)			
chr4	4267700	4290194	4p16.3	4p16.3		617684	LYAR	"Ly1 antibody-reactive protein, mouse, homolog of"	LYAR	55646	ENSG00000145220			Lyar (MGI:107470)			
chr4	4290196	4321785	4p16.3	4p16.3		616238	"ZBTB49, ZNF509"	Zinc finger- and BTB domain-containing protein 49	ZBTB49	166793	ENSG00000168826			Zbtb49 (MGI:1922329)			
chr4	4386255	4419057	4p16.3	4p16.3		607645	"D4S234E, D4S234"	D4S234E gene	NSG1	27065	ENSG00000168824			Nsg1 (MGI:109149)			
chr4	4859664	4863935	4p16.1	4p16.2		142983	"MSX1, HOX7, HYD1, OFC5, STHAG1, ECTD3"	"Muscle segment homeo box, Drosophila, homolog of, 1 (homeo box 7)"	MSX1	4487	ENSG00000163132		"Ectodermal dysplasia 3, Witkop type, 189500 (3), Autosomal dominant; Orofacial cleft 5, 608874 (3); Tooth agenesis, selective, 1, with or without orofacial cleft, 106600 (3), Autosomal dominant"	Msx1 (MGI:97168)			
chr4	5014585	5019469	4p16.2	4p16.2		607930	"CYTL1, C17"	Cytokine-like protein 1	CYTL1	54360	ENSG00000170891			Cytl1 (MGI:2684993)			
chr4	5562407	5709547	4p16	4p16.2		607261	"EVC2, LBN, WAD"	EVC2 (limbin) gene	EVC2	132884	ENSG00000173040		"Ellis-van Creveld syndrome, 225500 (3), Autosomal recessive; Weyers acrofacial dysostosis, 193530 (3), Autosomal dominant"	Evc2 (MGI:1915775)			
chr4	5711196	5829042	4p16	4p16.2		604831	EVC	EVC gene	EVC	2121	ENSG00000072840	mutation identified in 1 WAD patient	"Ellis-van Creveld syndrome, 225500 (3), Autosomal recessive; ?Weyers acrofacial dysostosis, 193530 (3), Autosomal dominant"	Evc (MGI:1890596)			
chr4	5820763	5893082	4p16.1-p15	4p16.2		602462	"CRMP1, DPYSL1, DRP1"	Collapsin response mediator protein-1	CRMP1	1400	ENSG00000072832			Crmp1 (MGI:107793)			
chr4	6024924	6200590	4p16.2	4p16.1		611195	"JAKMIP1, JAMIP1, MARLIN1"	Janus kinase and microtubule-interacting protein 1	JAKMIP1	152789	ENSG00000152969			Jakmip1 (MGI:1923321)			
chr4	6260367	6303264	4p16.1	4p16.1		606201	"WFS1, WFRS, WFS, DFNA6, DFNA14, DFNA38, WFSL, CTRCT41"	Wolframin	WFS1	7466	ENSG00000109501	mutation identified in 1 CTRCT41 family	"?Cataract 41, 116400 (3), Autosomal dominant; Deafness, autosomal dominant 6/14/38, 600965 (3), Autosomal dominant; {Diabetes mellitus, noninsulin-dependent, association with}, 125853 (3), Autosomal dominant; Wolfram syndrome 1, 222300 (3), Autosomal recessive; Wolfram-like syndrome, autosomal dominant, 614296 (3), Autosomal dominant"	Wfs1 (MGI:1328355)			
chr4	6320577	6563599	4p16	4p16.1		605997	"PPP2R2C, PR52"	"Protein phosphatase 2A, regulatory subunit B, gamma isoform"	PPP2R2C	5522	ENSG00000074211			Ppp2r2c (MGI:2442660)			
chr4	6640090	6642744	4p16.1	4p16.1		616905	"MRFAP1, PAM14, PGR1`"	MORF4 family- associated protein 1	MRFAP1	93621	ENSG00000179010			Mrfap1 (MGI:1914818)			
chr4	6693838	6697169	4p16	4p16.1		600614	S100P	S100 calcium-binding protein P	S100P	6286	ENSG00000163993						
chr4	6716114	6717659	4p16.1	4p16.1		605695	"BLOC1S4, BLOS4, CNO"	"Biogenesis of lysosome-related organelles complex 1, subunit 4"	BLOC1S4	55330	ENSG00000186222			Bloc1s4 (MGI:1929230)			
chr4	6909443	7033117	4p16.1	4p16.1		614855	"TBC1D14, KIAA1322"	"TBC1 domain family, member 14"	TBC1D14	57533	ENSG00000132405			Tbc1d14 (MGI:1098708)			
chr4	7043428	7057951	4p16.1	4p16.1		608790	"TADA2B, ADA2B"	Transcriptional adaptor 2B	TADA2B	93624	ENSG00000173011			Tada2b (MGI:3035274)			
chr4	7058894	7068209	4p16	4p16.1		606173	"GRPEL1, HMGE"	"GrpE, E. coli, homolog of"	GRPEL1	80273	ENSG00000109519			Grpel1 (MGI:1334417)			
chr4	7192606	7742836	4p16.1	4p16.1		606284	"SORCS2, KIAA1329"	SORCS receptor 2	SORCS2	57537	ENSG00000184985			Sorcs2 (MGI:1932289)			
chr4	7758712	7939925	4p16.1	4p16.1		608252	"AFAP1, AFAP, AFAP110"	Actin filament-associated protein 1	AFAP1	60312	ENSG00000196526			Afap1 (MGI:1917542)			
chr4	7965309	8158831	4p16	4p16.1		612544	"ABLIM2, KIAA1808"	"Actin-binding LIM protein family, member 2"	ABLIM2	84448	ENSG00000163995			Ablim2 (MGI:2385758)			
chr4	8005300	8005380	Chr.4	4p16.1		613185	"MIR95, MIRN95"	Micro RNA 95	MIR95	407052							
chr4	8269711	8307110	4p16.1	4p16.1		608785	"HTRA3, PRSP"	HTRA serine peptidase 3	HTRA3	94031	ENSG00000170801			Htra3 (MGI:1925808)			
chr4	8366262	8440724	4p15.3	4p16.1		603402	ACOX3	"Acyl-coenzyme A oxidase 3, pristanoyl"	ACOX3	8310	ENSG00000087008			Acox3 (MGI:1933156)			
chr4	8440773	8512530	4p15	4p16.1		614309	METTL19	Methyltransferase-like 19	TRMT44	152992	ENSG00000155275			Trmt44 (MGI:1926140)			
chr4	8580236	8590022	4p16.1	4p16.1		606921	GPR78	G protein-coupled receptor 78	GPR78	27201	ENSG00000155269						
chr4	8592659	8619760	4p16.1	4p16.1		603105	CPZ	Carboxypeptidase Z	CPZ	8532	ENSG00000109625			Cpz (MGI:88487)			
chr4	8846075	8871816	4p16.1	4p16.1		142992	"HMX1, H6"	Homeo box (H6 family) 1	HMX1	3166	ENSG00000215612		"Oculoauricular syndrome, 612109 (3), Autosomal recessive"	Hmx1 (MGI:107178)			
chr4	9358381	9359973	4p16.1	4p16.1		607011	"USP17L9P, USP17"	"Ubiquitin-specific protease 17-like family member 9, pseudogene"	USP17L9P	391627							
chr4	9771124	10040247	4p16-p15.3	4p16.1		606142	"SLC2A9, GLUT9, UAQTL2"	"Solute carrier family 2 (facilitated glucose transporter), member 9"	SLC2A9	56606	ENSG00000109667		"Hypouricemia, renal, 2, 612076 (3), Autosomal recessive, Autosomal dominant; {Uric acid concentration, serum, QTL 2}, 612076 (3), Autosomal recessive, Autosomal dominant"	Slc2a9 (MGI:2152844)			
chr4	9781633	9784008	4p16.1-p15.3	4p16.1		126453	"DRD5, DRD1B, DRD1L2"	Dopamine receptor D5	DRD5	1816	ENSG00000169676	pseudogenes on 2p11 and 1q21	"{Attention deficit-hyperactivity disorder, susceptibility to}, 143465 (3), Autosomal dominant; {Blepharospasm, primary benign}, 606798 (3), Isolated cases; Dystonia, primary cervical (3)"	Drd5 (MGI:94927)			
chr4	10074338	10117033	4p	4p16.1		604734	WDR1	WD repeat-containing protein 1	WDR1	9948	ENSG00000071127			Wdr1 (MGI:1337100)			
chr4	10439879	10457422	4p16.1	4p16.1		617734	"ZNF518B, KIAA1729"	Zinc finger protein 518B	ZNF518B	85460	ENSG00000178163			Zfp518b (MGI:2140750)			
chr4	10486404	10734852	4p16.1	4p16.1		611434	"CLNK, MIST"	Cytokine-dependent hematopoietic cell linker	CLNK	116449	ENSG00000109684			Clnk (MGI:1351468)			
chr4	11300000	41200000	4p15-p14			608410	BMIQ7	Body mass index quantitative trait locus 7		404683			"{Obesity, susceptibility to, BMIQ7}, 608410 (2)"				
chr4	11300000	35800000	4p15			607221	EPPS	"Epilepsy, partial, with pericentral spikes"		266789			"Epilepsy, partial, with pericentral spikes, 607221 (2)"				
chr4	11300000	21300000	4p15.3			604802	"HDL3, HLN2"	Huntington disease-like 3		53369			"Huntington disease-like 3, 604802 (2), Autosomal recessive"				
chr4	11300000	21300000	4p15.3			612226	STQTL13	Stature quantitative trait locus 13		100270796		associated with rs16896068	"{Stature QTL 13}, 612226 (2)"				
chr4	11393149	11434397	4p15.33	4p15.33		603244	"HS3ST1, 3OST, 3OST1"	Heparan sulfate (glucosamine)3-O-sulfotransferase 1	HS3ST1	9957	ENSG00000002587			Hs3st1 (MGI:1201606)			
chr4	13367722	13484364	4p15.33	4p15.33		612994	"RAB28, CORD18"	Ras-associated protein 28	RAB28	9364	ENSG00000157869		"Cone-rod dystrophy 18, 615374 (3), Autosomal recessive"	Rab28 (MGI:1917285)			
chr4	13540829	13544489	4p16.1	4p15.33		602183	"NKX3-2, BAPX1, SMMD"	"Bagpipe homeo box, Drosophila, homolog of"	NKX3-2	579	ENSG00000109705		"Spondylo-megaepiphyseal-metaphyseal dysplasia, 613330 (3), Autosomal recessive"	Nkx3-2 (MGI:108015)			
chr4	13568737	13627720	4p16.1	4p15.33		616746	"BOD1L1, FAM44A"	BOD1-like protein 1	BOD1L1	259282	ENSG00000038219			Bod1l (MGI:2444804)			
chr4	15002425	15070152	4q32-q33	4p15.32		610605	CPEB2	Cytoplasmic polyadenylation element-binding protein 2	CPEB2	132864	ENSG00000137449			Cpeb2 (MGI:2442640)			
chr4	15468659	15601970	4p15.3	4p15.32		612013	"CC2D2A, KIAA1345, MKS6"	Coiled-coil and C2 domains-containing protein 2A	CC2D2A	57545	ENSG00000048342		"COACH syndrome, 216360 (3), Autosomal recessive; Joubert syndrome 9, 612285 (3), Autosomal recessive; Meckel syndrome 6, 612284 (3), Autosomal recessive"	Cc2d2a (MGI:1924487)			
chr4	15604383	15681543	4p15.33	4p15.32		605655	"FBXL5, FBL5"	F-box and leucine-rich repeat protein 5	FBXL5	26234	ENSG00000118564			Fbxl5 (MGI:2152883)			
chr4	15701865	15774177	4p15.32	4p15.32		600387	BST1	Bone marrow stromal cell antigen 1	BST1	683	ENSG00000109743	previously assigned to 14q32.3		Bst1 (MGI:105370)			
chr4	15778264	15853242	4p15	4p15.32		107270	CD38	CD38 antigen (p45); ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase	CD38	952	ENSG00000004468			Cd38 (MGI:107474)			
chr4	15935568	15938739	4p15.3	4p15.32		607737	"FGFBP1, FGFBP, HBP17"	Fibroblast growth factor-binding protein 1	FGFBP1	9982	ENSG00000137440			Fgfbp1 (MGI:1096350)			
chr4	15960239	15963235	4p16	4p15.32		607713	KSP37	"Killer-specific secretory protein, 37kD"	FGFBP2	83888	ENSG00000137441						
chr4	15968225	16084058	4p15.3	4p15.32		604365	"PROM1, PROML1, AC133, RP41, CORD12, CD133, MCDR2, STGD4"	Prominin 1	PROM1	8842	ENSG00000007062		"Cone-rod dystrophy 12, 612657 (3); Macular dystrophy, retinal, 2, 608051 (3), Autosomal dominant; Retinitis pigmentosa 41, 612095 (3), Autosomal recessive; Stargardt disease 4, 603786 (3)"	Prom1 (MGI:1100886)			
chr4	16160504	16226537	4p15.32	4p15.32		612758	"TAPT1, CMVFR, OCLSBG"	Transmembrane anterior posterior transformation 1	TAPT1	202018	ENSG00000169762		"Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type, 616897 (3), Autosomal recessive"	Tapt1 (MGI:2683537)			
chr4	16501533	16898808	4p15	4p15.32		603450	"LDB2, CLIM1"	LIM domain-binding factor-2	LDB2	9079	ENSG00000169744			Ldb2 (MGI:894670)			
chr4	17486392	17512233	4p15.31	4p15.32		612676	"QDPR, DHPR"	Quinoid dihydropteridine reductase	QDPR	5860	ENSG00000151552		"Hyperphenylalaninemia, BH4-deficient, C, 261630 (3), Autosomal recessive"	Qdpr (MGI:97836)			
chr4	17577303	17607966	4p11-q12	4p15.32		170250	PEPS	Peptidase S	LAP3	51056	ENSG00000002549			Lap3 (MGI:1914238)			
chr4	17614627	17625627	4p15.32	4p15.32		610311	"MED28, EG1, MAGICIN"	Mediator complex subunit 28	MED28	80306	ENSG00000118579			Med28 (MGI:1914249)			
chr4	17810812	17844864	4p15.3	4p15.31		606280	"NCAPG, CAPG"	Non-SMC condensin I complex subunit G	NCAPG	64151	ENSG00000109805			Ncapg (MGI:1930197)			
chr4	17841198	18023286	4p15.3	4p15.31		611799	"LCORL, MLR1"	Ligand-dependent nuclear receptor corepressor-like protein	LCORL	254251	ENSG00000178177			Lcorl (MGI:2651932)			
chr4	20251904	20620560	4p15.2	4p15.31		603746	SLIT2	"Slit, Drosophila, homolog of, 2"	SLIT2	9353	ENSG00000145147			Slit2 (MGI:1315205)			
chr4	20528274	20528383	4p15.31	4p15.31		616770	MIR218-1	Micro RNA 218-1	MIR218-1	407000		within intron of SLIT2					
chr4	20728519	21948750	4p15.3	4p15.3-p15.2		608182	"KCNIP4, KCHIP4"	Kv channel-interacting protein 4	KCNIP4	80333	ENSG00000185774			Kcnip4 (MGI:1933131)			
chr4	22387373	22516057	4p15.2	4p15.2		612303	"ADGRA3, GPR125"	Adhesion G protein-coupled receptor A3	ADGRA3	166647	ENSG00000152990			Adgra3 (MGI:1917943)			
chr4	22692913	22819574	4p15.31	4p15.2		606619	"GBA3, CBGL1"	"Glucosidase, beta, acid 3"	GBA3	57733	ENSG00000249948						
chr4	23792020	24472828	4p15.1	4p15.2		604517	"PPARGC1A, PPARGC1"	"Peroxisome proliferator-activated receptor-gamma, coactivator 1, alpha"	PPARGC1A	10891	ENSG00000109819			Ppargc1a (MGI:1342774)			
chr4	24527463	24584560	4p15.3	4p15.2		603403	"DHX15, DDX15, DBP1, HRH2"	DEAH (Asp-Glu-Ala-His) box polypeptide 15	DHX15	1665	ENSG00000109606			Dhx15 (MGI:1099786)			
chr4	24795462	24800844	4p15.3-p15.1	4p15.2		185490	SOD3	"Superoxide dismutase-3, extracellular"	SOD3	6649	ENSG00000109610		"[Superoxide dismutase, elevated extracellular] (3)"	Sod3 (MGI:103181)			
chr4	24991959	25030791	4p15.2	4p15.2		608301	"LGI2, KIAA1916"	"Leucine-rich gene, glioma-inactivated, 2"	LGI2	55203	ENSG00000153012			Lgi2 (MGI:2180196)			
chr4	25120004	25160581	4p15.2	4p15.2		613009	"SEPSECS, SLA, LP, PCH2D"	O-phosphoserine tRNA-selenocysteine tRNA synthase	SEPSECS	51091	ENSG00000109618		"Pontocerebellar hypoplasia type 2D, 613811 (3), Autosomal recessive"	Sepsecs (MGI:1098791)			
chr4	25234030	25279208	4p15.2	4p15.2		612101	PI4K2B	"Phosphatidylinositol 4-kinase, type 2, beta"	PI4K2B	55300	ENSG00000281028			Pi4k2b (MGI:1914323)			
chr4	25312773	25373175	4p15.2	4p15.2		611792	ZCCHC4	Zinc finger CCHC domain-containing protein 4	ZCCHC4	29063	ENSG00000168228			Zcchc4 (MGI:1926046)			
chr4	25377225	25418497	4p15.2	4p15.2		606947	"ANAPC4, APC4"	"Anaphase-promoting complex, subunit 4"	ANAPC4	29945	ENSG00000053900			Anapc4 (MGI:1098673)			
chr4	25655812	25678747	4p15.31-p15.2	4p15.2		604217	SLC34A2	"Solute carrier family 34 (sodium/phosphate cotransporter), member 2"	SLC34A2	10568	ENSG00000157765		"Pulmonary alveolar microlithiasis, 265100 (3), Autosomal recessive"	Slc34a2 (MGI:1342284)			
chr4	25914191	25929878	4p15.2	4p15.2		617465	"SMIM20, MITRAC7, C4orf52"	Small integral membrane protein 20	SMIM20	389203	ENSG00000250317			Smim20 (MGI:1913528)			
chr4	26163488	26435130	4p15.2	4p15.2		147183	"RBPJ, RBPSUH, IGKJRB1, AOS3"	Recombination signal-binding protein 1 for kappa J region	RBPJ	3516	ENSG00000168214	"pseudogenes at 9q13, 9p13, and 3q25"	"Adams-Oliver syndrome 3, 614814 (3), Autosomal dominant"	Rbpj (MGI:96522)			
chr4	26481395	26490419	4p15.2-p15.1	4p15.2		118444	CCKAR	Cholecystokinin A receptor	CCKAR	886	ENSG00000163394			Cckar (MGI:99478)			
chr4	26860690	27025380	4p15.1	4p15.2		610841	"STIM2, KIAA1482"	Stromal interaction molecule 2	STIM2	57620	ENSG00000109689			Stim2 (MGI:2151156)			
chr4	27700000	58500000	4p15.1-q12			607107	"NPC1, NPCA1"	Nasopharyngeal carcinoma 1		257641		?associated with acyl-CoA thioesterase 7-like	"{Nasopharyngeal carcinoma 1}, 607107 (2)"				
chr4	30719860	31146800	4p15	4p15.1		602988	"PCDH7, BHPCDH"	Protocadherin-7	PCDH7	5099	ENSG00000169851			Pcdh7 (MGI:1860487)			
chr4	35800000	41200000	4p14			614991	UCH1LAS	"Ubiquitin carboxyl-terminal esterase L1, antisense"		101180899							
chr4	36005185	36244832	4p14	4p14		606645	"ARAP2, CENTD1, KIAA0580"	"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2"	ARAP2	116984	ENSG00000047365			Arap2 (MGI:2684416)			
chr4	36281592	36347510	4p14	4p14		616979	DTHD1	Death domain-containing protein 1	DTHD1	401124	ENSG00000197057			Dthd1 (MGI:4937018)			
chr4	37590799	37686402	4p14	4p14		611212	RELL1	Relt-like 1	RELL1	768211	ENSG00000181826			Rell1 (MGI:2140767)			
chr4	37826659	37862937	4p14-q12	4p14		172000	PGM2	Phosphoglucomutase-2	PGM2	55276	ENSG00000169299			Pgm1 (MGI:97564)			
chr4	37891083	38139174	4p15.1-q21	4p14		609850	"TBC1D1, KIAA1108"	"TBC1 domain family, member 1"	TBC1D1	23216	ENSG00000065882			Tbc1d1 (MGI:1889508)			
chr4	37960434	37961009	4p12	4p14		604231	PTTG2	Pituitary tumor-transforming gene 2	PTTG2	10744	ENSG00000250254						
chr4	38664078	38701507	4p14	4p14		609392	"KLF3, BKLF"	Kruppel-like factor 3	KLF3	51274	ENSG00000109787			Klf3 (MGI:1342773)			
chr4	38791054	38806261	4p14	4p14		601194	"TLR1, TIL. LPRS5"	Toll-like receptor-1	TLR1	7096	ENSG00000174125		"{Leprosy, protection against}, 613223 (3); {Leprosy, susceptibility to, 5}, 613223 (3)"	Tlr1 (MGI:1341295)			
chr4	38823679	38857766	4p14	4p14		605403	TLR6	Toll-like receptor 6	TLR6	10333	ENSG00000174130			Tlr6 (MGI:1341296)			
chr4	38868031	38868126	4p14	4p14		615469	"MIR574, MIR574-3p"	Micro RNA 574	MIR574	693159							
chr4	39044673	39143100	4p15.1-p13	4p14		608064	KLHL5	Kelch-like 5	KLHL5	51088	ENSG00000109790			Klhl5 (MGI:1919028)			
chr4	39182403	39285809	4p14-p11	4p14		608151	"WDR19, SRTD5, ATD5, NPHP13, CED4"	WD repeat-containing protein 19	WDR19	57728	ENSG00000157796	mutation identified in 1 CED4 family and 1 SRTD5 family	"?Cranioectodermal dysplasia 4, 614378 (3), Autosomal recessive; Nephronophthisis 13, 614377 (3), Autosomal recessive; Senior-Loken syndrome 8, 616307 (3), Autosomal recessive; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 (3), Autosomal recessive"	Wdr19 (MGI:2443231)			
chr4	39287448	39366380	4p14-p13	4p14		102579	"RFC1, RECC1"	"Replication factor C1, 145kD (activator 1, 145kD)"	RFC1	5981	ENSG00000035928			Rfc1 (MGI:97891)			
chr4	39406852	39451532	4p14	4p14		611135	"KLB, BKL"	"Klotho, beta"	KLB	152831	ENSG00000134962			Klb (MGI:1932466)			
chr4	39454123	39458947	4p13	4p14		603686	RPL9	Ribosomal protein L9	RPL9	6133	ENSG00000163682	pseudogene on Xpter-p21		Rpl9 (MGI:1298373)			
chr4	39459021	39477652	4p14	4p14		607031	"LIAS, PDHLD, HGCLAS"	Lipoic acid synthase	LIAS	11019	ENSG00000121897		"Hyperglycinemia, lactic acidosis, and seizures, 614462 (3), Autosomal recessive"	Lias (MGI:1934604)			
chr4	39498754	39527597	4p15.1	4p14		603370	"UGDH, UDPGDH"	UDP-glucose dehydrogenase	UGDH	7358	ENSG00000109814			Ugdh (MGI:1306785)			
chr4	39698043	39782791	4p14	4p14		602846	HIP2	Huntingtin-interacting protein-2	UBE2K	3093	ENSG00000078140			Ube2k (MGI:1858216)			
chr4	39822862	39977955	4p14	4p14		613200	"PDS5A, KIAA0648, SCC112"	"PDS5, regulator of cohesion maintenance, S. Cerevisiae, homolog of, A"	PDS5A	23244	ENSG00000121892			Pds5a (MGI:1918771)			
chr4	40042916	40057198	4p14-p11	4p14		611963	LOC344967	Acyl-CoA thioesterase 7-like		344967		?associated with nasopharyngeal carcinoma					
chr4	40191010	40244763	4p13	4p14		602037	"ARHH, TTF"	"Ras homolog gene family, member H"	RHOH	399	ENSG00000168421			Rhoh (MGI:1921984)			
chr4	40335328	40355216	4p15.1-p14	4p14		605116	CHRNA9	"Cholinergic receptor, neuronal nicotinic, alpha polypeptide 9"	CHRNA9	55584	ENSG00000174343			Chrna9 (MGI:1202403)			
chr4	40749873	40815728	4p14	4p14		617185	NSUN7	"NOP2/SUN RNA methyltransferase family, member 7"	NSUN7	79730	ENSG00000179299			Nsun7 (MGI:1918168)			
chr4	40810026	41216713	4p14	4p14-p13		602710	"APBB2, FE65L1"	"Amyloid beta A4 precursor protein-binding, family B, member 2 (Fe65-like 1)"	APBB2	323	ENSG00000163697			Apbb2 (MGI:108405)			
chr4	41200000	87100000	4p13-q21			605841	NRCLP2	Narcolepsy 2		100918		max lod at D4S2987	"Narcolepsy 2, 605841 (2)"				
chr4	41256880	41268428	4p14	4p13		191342	"UCHL1, PARK5, SPG79, NDGOA"	Ubiquitin C-terminal esterase L1	UCHL1	7345	ENSG00000154277	mutation identified in 1 PARK5 family	"{?Parkinson disease 5, susceptibility to}, 613643 (3); Spastic paraplegia 79, autosomal recessive, 615491 (3), Autosomal recessive"	Uchl1 (MGI:103149)			
chr4	41359606	41700043	4p13	4p13		617750	"LIMCH1, LMO7B"	LIM and calponin homology domains-containing protein 1	LIMCH1	22998	ENSG00000064042			Limch1 (MGI:1924819)			
chr4	41744081	41748969	4p12	4p13		603851	"PHOX2B, NBPHOX, PMX2B, NBLST2, CCHS"	Paired mesoderm homeo box 2B	PHOX2B	8929	ENSG00000109132		"Central hypoventilation syndrome, congenital, with or without Hirschsprung disease, 209880 (3), Autosomal dominant; Neuroblastoma with Hirschsprung disease, 613013 (3); {Neuroblastoma, susceptibility to, 2}, 613013 (3)"	Phox2b (MGI:1100882)			
chr4	41990501	42087533	4p13	4p13		604604	"SLC30A9, C4orf1, HUEL, BILAPES"	"Solute carrier family 30 (zinc transporter), member 9"	SLC30A9	10463	ENSG00000014824	mutation identified in 1 BILAPES family	"?Birk-Landau-Perez syndrome, 617595 (3), Autosomal recessive"	Slc30a9 (MGI:1923690)			
chr4	42397323	42402486	4p13	4p13		617325	SHISA3	"Shisa family, member 3"	SHISA3	152573	ENSG00000178343			Shisa3 (MGI:3041225)			
chr4	42893265	43030657	4p13	4p13		613283	GRXCR1	"Glutaredoxin, cysteine-rich, 1"	GRXCR1	389207	ENSG00000215203		"Deafness, autosomal recessive 25, 613285 (3), Autosomal recessive"	Grxcr1 (MGI:3577767)			
chr4	44678394	44700680	4p12	4p12		617064	"GUF1, EF4, EIEE40"	"GTPase, S. cerevisiae, homolog of"	GUF1	60558	ENSG00000151806	mutation identified in 1 EIEE40 family	"?Epileptic encephalopathy, early infantile, 40, 617065 (3), Autosomal recessive"	Guf1 (MGI:2140726)			
chr4	44701794	44726633	4p13	4p12		613222	"GNPDA2, GNP2"	Glucosamine-6-phosphate deaminase 2	GNPDA2	132789	ENSG00000163281			Gnpda2 (MGI:1915230)			
chr4	46035768	46124064	4p14-q21.1	4p12		137166	GABRG1	"Gamma-aminobutyric acid (GABA) A receptor, gamma-1"	GABRG1	2565	ENSG00000163285			Gabrg1 (MGI:103156)			
chr4	46243547	46390348	4p13-p12	4p12		137140	GABRA2	"Gamma-aminobutyric acid (GABA) A receptor, alpha-2"	GABRA2	2555	ENSG00000151834		"{Alcohol dependence, susceptibility to}, 103780 (3), Multifactorial"	Gabra2 (MGI:95614)			
chr4	46734826	46909265	4p12	4p12		609811	COX7B2	Cytochrome C oxidase subunit VIIb2	COX7B2	170712	ENSG00000170516						
chr4	46918899	46994406	4p14-q12	4p12		137141	GABRA4	"Gamma-aminobutyric acid (GABA) A receptor, alpha-4"	GABRA4	2557	ENSG00000109158	"cluster with GABRA2, B1, G1; ?involved in autism"		Gabra4 (MGI:95616)			
chr4	46993559	47438408	4p13-p12	4p12		137190	"GABRB1, EIEE45"	"Gamma-aminobutyric acid (GABA) A receptor, beta-1"	GABRB1	2560	ENSG00000163288		"Epileptic encephalopathy, early infantile, 45, 617153 (3), Autosomal dominant"	Gabrb1 (MGI:95619)			
chr4	47450786	47463729	4p12	4p12		616656	COMMD8	COMM domain-containing protein 8	COMMD8	54951	ENSG00000169019			Commd8 (MGI:1343485)			
chr4	47593997	47838105	4p12	4p12		605236	"CORIN, CRN, TMPRSS10, ATC2, PEE5"	"Corin, serine peptidase"	CORIN	10699	ENSG00000145244		"Preeclampsia/eclampsia 5, 614595 (3)"	Corin (MGI:1349451)			
chr4	47935014	48016717	4p12-cen	4p12		123825	"CNGA1, CNCG1, RP49"	"Cyclic nucleotide gated channel, alpha 1"	CNGA1	1259	ENSG00000198515		"Retinitis pigmentosa 49, 613756 (3)"	Cnga1 (MGI:88436)			
chr4	48063503	48135321	4p12	4p12		600058	"TXK, BTKL"	TXK tyrosine kinase	TXK	7294	ENSG00000074966			Txk (MGI:102960)			
chr4	48135782	48269863	4p12	4p12-p11		600583	TEC	tec protein tyrosine kinase	TEC	7006	ENSG00000135605			Tec (MGI:98662)			
chr4	48341474	48426197	4p11	4p11		610492	"SLAIN2, KIAA1458"	"SLAIN motif family, member 2"	SLAIN2	57606	ENSG00000109171			Slain2 (MGI:1923241)			
chr4	48490251	48499350	4p11	4p11		607520	ZAR1	Zygote arrest 1	ZAR1	326340	ENSG00000182223			Zar1 (MGI:2180337)			
chr4	50000000	190214555	4q			603664	MHW2	Mental health wellness 2		50979		at D4S397	"{Mental health wellness-2}, 603664 (2)"				
chr4	50000000	190214555	4q			601454	PSORS3	Psoriasis susceptibility 3	PSORS3	7889			"{Psoriasis susceptibility 3}, 601454 (2)"				
chr4	50000000	190214555	4q			610430	WM2	"Macroglobulinemia, Waldenstrom, susceptibility to, 2"		100188811		between D4S2910 and D4S1539	"{Macroglobulinemia, Waldenstrom, susceptibility to, 2}, 610430 (2)"				
chr4	51800000	65500000	4q12-q13.1			612431	DFNA27	"Deafness, autosomal dominant 27"	DFNA27	23722		max lod at D4S398	"Deafness, autosomal dominant 27, 612431 (2), Autosomal dominant"				
chr4	51800000	69400000	4q12-q13.2			609952	DFNB55	"Deafness, autosomal recessive 55"	DFNB55	494148		max lod at D4S2638	"Deafness, autosomal recessive 55, 609952 (2), Autosomal recessive"				
chr4	51800000	65500000	4q12-q13.1			614329	MRT31	"Mental retardation, autosomal recessive 31"		100852399		between rs11944876 and rs6551838	"Mental retardation, autosomal recessive 31, 614329 (2), Autosomal recessive"				
chr4	51800000	58500000	4q12			609258	MYP9	Myopia 9	MYP9	553194			"Myopia 9, 609258 (2), Multifactorial"				
chr4	51800000	58500000	4q12			106700	TAPVR1	Total anomalous pulmonary venous return 1	TAPVR1	6893		between D4S1630 and D4S3019; ?mutation in KDR	"Total anomalous pulmonary venous return, 106700 (2), Autosomal dominant"				
chr4	51842999	51916836	4q12	4q12		612977	"DCUN1D4, KIAA0276"	DCN1 domain-containing protein 4	DCUN1D4	23142	ENSG00000109184			Dcun1d4 (MGI:2140972)			
chr4	52020694	52038318	4q12	4q12		600900	"SGCB, LGMD2E"	"Sarcoglycan, beta (43kD dystrophin-associated glycoprotein)"	SGCB	6443	ENSG00000163069		"Muscular dystrophy, limb-girdle, type 2E, 604286 (3), Autosomal recessive"	Sgcb (MGI:1346523)			
chr4	52051330	52097304	4q11-q12	4q12		612814	"SPATA18, SPETEX1"	Spermatogenesis-associated protein 18	SPATA18	132671	ENSG00000163071			Spata18 (MGI:1920722)			
chr4	52590959	52659334	4q12	4q12		612849	USP46	Ubiquitin-specific peptidase 46	USP46	64854	ENSG00000109189			Usp46 (MGI:1916977)			
chr4	52712393	52720696	4q12	4q12		614625	"DANCR, ANCR, KIAA0114"	Differentiation-antagonizing noncoding RNA	DANCR	57291							
chr4	52712681	52712746	4q12	4q12		614627	MIR4449	Micro RNA 4449	MIR4449	100616436							
chr4	52713248	52713369	4q12	4q12		614626	SNORA26	"Small nucleolar RNA, H/ACA box, 26"	SNORA26	677810							
chr4	52862327	52866834	4q12	4q12		612404	RASL11B	"RAS-like, family 11, member B"	RASL11B	65997	ENSG00000128045			Rasl11b (MGI:1916189)			
chr4	53377571	53462610	4q12	4q12		607686	FIP1L1	Fip1-like 1	FIP1L1	81608	ENSG00000145216	fused to PDGFRA in hypereosinophilic syndrome					
chr4	53458263	53652524	4q12	4q12		609732	"LNX1, LNX, PDZRN2"	Ligand of numb protein X1	LNX1	84708	ENSG00000072201			Lnx1 (MGI:1278335)			
chr4	53996334	54064689	4q11-q12	4q12		604332	"CHIC2, BTL"	Cysteine-rich hydrophobic domain 2 (Brx-like gene translocated in leukemia)	CHIC2	26511	ENSG00000109220		"{Leukemia, acute myeloid}, 601626 (3), Autosomal dominant"	Chic2 (MGI:1921527)			
chr4	54100080	54101954	4q12	4q12		616253	"GSX2, GSH2"	GS homeobox 2	GSX2	170825	ENSG00000180613			Gsx2 (MGI:95843)			
chr4	54229088	54298246	4q12	4q12		173490	PDGFRA	"Platelet-derived growth factor receptor, alpha polypeptide"	PDGFRA	5156	ENSG00000134853	same 700bp segment as KIT; fused to BCR or FIP1L1	"Gastrointestinal stromal tumor, somatic, 606764 (3); Hypereosinophilic syndrome, idiopathic, resistant to imatinib, 607685 (3), Isolated cases, Somatic mutation"	Pdgfra (MGI:97530)			
chr4	54657927	54740714	4q12	4q12		164920	"KIT, PBT"	Hardy-Zuckerman 4 feline sarcoma (v-kit) oncogene	KIT	3815	ENSG00000157404	same 700bp segment as PDGFRA	"Gastrointestinal stromal tumor, familial, 606764 (3), Autosomal dominant, Isolated cases; Germ cell tumors, somatic, 273300 (3); Leukemia, acute myeloid, 601626 (3), Autosomal dominant; Mast cell disease, 154800 (3), Autosomal dominant; Piebaldism, 172800 (3), Autosomal dominant"	Kit (MGI:96677)			
chr4	55078480	55125594	4q12	4q12		191306	KDR	Kinase insert domain receptor	KDR	3791	ENSG00000128052	?mutant in TAPVR1	"Hemangioma, capillary infantile, somatic, 602089 (3); {Hemangioma, capillary infantile, susceptibility to}, 602089 (3), Autosomal dominant"	Kdr (MGI:96683)			
chr4	55346220	55373099	4q12	4q12		611715	"SRD5A3, SRD5A2L, CDG1Q, KRIZI"	Steroid 5-alpha-reductase 3	SRD5A3	79644	ENSG00000128039		"Congenital disorder of glycosylation, type Iq, 612379 (3), Autosomal recessive; Kahrizi syndrome, 612713 (3), Autosomal recessive"	Srd5a3 (MGI:1930252)			
chr4	55395652	55453396	4q12	4q12		614726	"TMEM165, FT27, CDG2K"	Transmembrane protein 165	TMEM165	55858	ENSG00000134851		"Congenital disorder of glycosylation, type IIk, 614727 (3), Autosomal recessive"	Tmem165 (MGI:894407)			
chr4	55427900	55547137	4q12	4q12		601851	CLOCK	Circadian locomotor output cycles kaput	CLOCK	9575	ENSG00000134852			Clock (MGI:99698)			
chr4	55556522	55592273	4q11	4q12		611676	PDCL2	Phosducin-like 2	PDCL2	132954	ENSG00000163440			Pdcl2 (MGI:1890655)			
chr4	55853647	55905077	4q12	4q12		607879	"EXOC1, SEC3"	Exocyst complex component 1	EXOC1	55763	ENSG00000090989			Exoc1 (MGI:2445020)			
chr4	55948807	56033362	4q12	4q12		611423	"CEP135, KIAA0635, MCPH8"	"Centrosomal protein, 135kD"	CEP135	9662	ENSG00000174799		"Microcephaly 8, primary, autosomal recessive, 614673 (3), Autosomal recessive"	Cep135 (MGI:2681869)			
chr4	56337686	56389417	4q12	4q12		614365	"AASDH, ACSF4"	Aminoadipate-semialdehyde dehydrogenase	AASDH	132949	ENSG00000157426			Aasdh (MGI:2442517)			
chr4	56393361	56435635	4q12	4q12		172450	"PPAT, GPAT"	Phosphoribosylpyrophosphate amidotransferase	PPAT	5471	ENSG00000128059			Ppat (MGI:2387203)			
chr4	56435748	56461367	4q12	4q12		172439	"PAICS, AIRC"	Phosphoribosylaminoimidazole carboxylase	PAICS	10606	ENSG00000128050	bifunctional enzyme; ade-D; 625bp from PPAT		Paics (MGI:1914304)			
chr4	56467595	56503680	4q12	4q12		602122	"SRP72, BMFS1"	"Signal recognition particle, 72kD"	SRP72	6731	ENSG00000174780		"Bone marrow failure syndrome 1, 614675 (3), Autosomal dominant"	Srp72 (MGI:1333795)			
chr4	56505208	56523982	4q12	4q12		612405	ARL9	ADP-ribosylation factor-like 9	ARL9	132946	ENSG00000196503			Arl9 (MGI:1915496)			
chr4	56647987	56681865	4q11-q12	4q12		607275	"HOPX, HOP"	HOP homeobox	HOPX	84525	ENSG00000171476			Hopx (MGI:1916782)			
chr4	56809859	56822209	4q12	4q12		605753	SPINK2	"Serine protease inhibitor, Kazal-type, 2"	SPINK2	6691	ENSG00000128040						
chr4	56907875	56935846	4q12	4q12		600571	"REST, NRSF, WT6, GINGF5, HGF5"	RE1-silencing transcription factor	REST	5978	ENSG00000084093		"Fibromatosis, gingival, 5, 617626 (3), Autosomal dominant; {Wilms tumor 6, susceptibility to}, 616806 (3)"	Rest (MGI:104897)			
chr4	56963343	56977659	4q12	4q12		614919	"NOA1, C4orf14"	Nitric oxide-associated protein 1	NOA1	84273	ENSG00000084092			Noa1 (MGI:1914306)			
chr4	56978639	57031161	4q12	4q12		180661	POL2RB	"Polymerase (RNA) II (DNA directed) polypeptide B, 140kD"	POLR2B	5431	ENSG00000047315			Polr2b (MGI:2388280)			
chr4	57031070	57110384	4q12	4q12		602867	"IGFBP7, MAC25, RAMSVPS"	Insulin-like growth factor-binding protein-7	IGFBP7	3490	ENSG00000163453		"Retinal arterial macroaneurysm with supravalvular pulmonic stenosis, 614224 (3), Autosomal recessive"	Igfbp7 (MGI:1352480)			
chr4	58500000	87100000	4q13-q21			609400	"AIS4, VAMAS5"	"Autoimmune disease, susceptibility to, 4"		619405		between D4S392 and D4S3042	"{Autoimmune disease, susceptibility to, 4}, 609400 (2)"				
chr4	61201255	62078334	4q13.1	4q13.1		616417	"ADGRL3, LPHN3, CIRL3, CL3, LEC3, KIAA0768"	Adhesion G protein-coupled receptor L3	ADGRL3	23284	ENSG00000150471			Adgrl3 (MGI:2441950)			
chr4	64276297	64409509	4q13.1	4q13.1		617242	"TECRL, TERL, SRD5A2L2, GPSN2L, CPVT3"	"Trans-2,3-enoyl-CoA reductase-like protein"	TECRL	253017	ENSG00000205678		"Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021 (3), Autosomal recessive"	Tecrl (MGI:2444966)			
chr4	65319562	65670494	4q13	4q13.1-q13.2		600004	"EPHA5, TYRO4, HEK7"	Ephrin receptor EphA5	EPHA5	2044	ENSG00000145242			Epha5 (MGI:99654)			
chr4	65500000	87100000	4q13.2-q21.3			611630	"ETL3, FMTLE"	"Epilepsy, familial temporal lobe, 3"		100188848		max lod at D4S1517	"Epilepsy, familial temporal lobe, 3, 611630 (2), Autosomal dominant"				
chr4	67468761	67545537	4q12-q13.3	4q13.2		117141	"CENPC1, CENPC"	Centromere autoantigen C1	CENPC	1060	ENSG00000145241	?pseudogene on chr.12		Cenpc1 (MGI:99700)			
chr4	67558696	67607340	4q13.2	4q13.2		604298	"STAP1, BRDG1"	Signal transducing adaptor family member 1	STAP1	26228	ENSG00000035720			Stap1 (MGI:1926193)			
chr4	67615760	67701170	4q13.2	4q13.2		611361	"UBA6, UBE1L2"	Ubiquitin activating enzyme 6	UBA6	55236	ENSG00000033178			Uba6 (MGI:1913894)			
chr4	67737374	67756085	4q21.2	4q13.2		138850	"GNRHR, LHRHR, HH7"	Gonadotropin-releasing hormone receptor	GNRHR	2798	ENSG00000109163	placed at 4q12 or 4q13 by some	"Hypogonadotropic hypogonadism 7 without anosmia, 146110 (3), Autosomal recessive"	Gnrhr (MGI:95790)			
chr4	67910300	67963513	4q13.2	4q13.2		611704	"TMPRSS11A, ECRG1"	"Transmembrane protease, serine 11A"	TMPRSS11A	339967	ENSG00000187054			Tmprss11a (MGI:2684853)			
chr4	68038415	68042510	4q12	4q13.2		608311	GRINL1B	"Glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B"	GCOM2	339970							
chr4	68060609	68063296	4q13.2	4q13.2		610892	"SYT14L, SYTDEP, CHR415SYT"	Synaptotagmin 14-like protein	SYT14P1	401135							
chr4	68310386	68350116	4q13.2	4q13.2		617283	"YTHDC1, KIAA1966"	TYH domain-containing protein 1	YTHDC1	91746	ENSG00000083896			Ythdc1 (MGI:2443713)			
chr4	68447448	68497603	4q13.2	4q13.2		610399	"TMPRSS11E, DESC1"	"Transmembrane protease, serine 11E"	TMPRSS11E	28983	ENSG00000087128			Tmprss11e (MGI:3513175)			
chr4	68537183	68576353	4q13	4q13.2		601903	"UGT2B17, BMND12"	"UDP-glucuronyltransferase, family 2, beta-17"	UGT2B17	7367	ENSG00000197888		"{Bone mineral density QTL 12, osteoporosis}, 612560 (3)"	Ugt2b1 (MGI:1919023)			
chr4	68646596	68670775	4q13	4q13.2		600069	"UGT2B15, UGT2B8"	"UDP-glucuronyltransferase, family 2, beta-15"	UGT2B15	7366	ENSG00000196620						
chr4	68815992	68832037	4q13.2	4q13.2		600070	UGT2B10	"Uridine diphosphate glycosyltransferase 2 family, member B10"	UGT2B10	7365	ENSG00000109181			Ugt2b34 (MGI:2140962)			
chr4	68928458	68951799	4q13	4q13.2		616382	UGT2A3	"Uridine diphosphate glucuronosyltransferase 2 family, member A3"	UGT2A3	79799	ENSG00000135220			Ugt2a3 (MGI:1919344)			
chr4	69051263	69112986	4q13	4q13.2		600068	"UGT2B7, UGT2B9"	"UDP-glucuronyltransferase, family 2, beta-7"	UGT2B7	7364	ENSG00000171234			"Ugt2b36,Ugt2b35 (MGI:3576103,MGI:3576100)"			
chr4	69200189	69224979	4q13.2	4q13.2		603064	UGT2B11	"Uridine diphosphate glycosyltransferase 2 family, member B11"	UGT2B11	10720	ENSG00000213759						
chr4	69280428	69295049	4q13.2	4q13.2		606497	UGT2B28	"Uridine diphosphate glycosyltransferase 2 family, member B28"	UGT2B28	54490	ENSG00000135226			"Ugt2b38,Ugt2b37,Ugt2b5 (MGI:2148239,MGI:2140794,MGI:98900)"			
chr4	69480164	69526013	4q13	4q13.3		600067	"UGT2B4, UGT2B11"	"UDP-glucuronyltransferase, family 2, beta-4"	UGT2B4	7363	ENSG00000156096	cluster in order B7--B4--B15 in 195kb					
chr4	69588416	69653248	4q13	4q13.3		604716	UGT2A1	"Uridine diphosphate glycosyltransferase 2 family, member A1"	UGT2A1	10941	ENSG00000173610			Ugt2a1 (MGI:2149905)			
chr4	69726847	69760711	4q13.3	4q13.3		608436	"SULT1B1, ST1B2"	"Sulfotransferase family 1B, member 1"	SULT1B1	27284	ENSG00000173597			Sult1b1 (MGI:2136282)			
chr4	69841211	69860151	4q13.1	4q13.3		600043	"STE, EST"	"Sulfotransferase, estrogen-preferring"	SULT1E1	6783	ENSG00000109193			Sult1e1 (MGI:98431)			
chr4	69931061	69946569	4q21.1	4q13.3		115450	CSN1	"Casein, alpha"	CSN1S1	1446	ENSG00000126545						
chr4	69955255	69965761	4q21.1	4q13.3		115460	CSN2	"Casein, beta"	CSN2	1447	ENSG00000135222			Csn2 (MGI:88541)			
chr4	69995930	70002455	4q11-q13	4q13.3		184470	STATH	Statherin	STATH	6779	ENSG00000126549						
chr4	70028412	70036537	4q13	4q13.3		142702	"HTN3, HTN2, HIS2"	Histatin-3	HTN3	3347	ENSG00000205649						
chr4	70050414	70058847	4q13	4q13.3		142701	HTN1	Histatin-1	HTN1	3346	ENSG00000126550	3 genes in a 15kb segment					
chr4	70195727	70204575	4q13.3	4q13.3		614843	"ODAM, APIN"	Odontogenic ameloblast-associated protein	ODAM	54959	ENSG00000109205			Odam (MGI:1916842)			
chr4	70238369	70251431	4q13-q21	4q13.3		601695	"CSN3, CNS10, CSNK"	"Casein, kappa"	CSN3	1448	ENSG00000171209			Csn3 (MGI:107461)			
chr4	70383077	70390243	4q13.3	4q13.3		611593	"SMR3B, SMR1B, PRL3, PBII"	"Submaxillary gland androgen-regulated protein 3, mouse, homolog of, B"	SMR3B	10879	ENSG00000171201						
chr4	70397881	70410196	4q13.3	4q13.3		608936	"PROL1, PRL1, BPLP"	Proline-rich lacrimal protein 1	OPRPN	58503	ENSG00000171199						
chr4	70430491	70482996	4q13-q21	4q13.3		158375	MUC7	"Mucin 7, salivary"	MUC7	4589	ENSG00000171195		"{Asthma, protection against}, 600807 (3), Autosomal dominant"				
chr4	70518571	70532742	4q13.3	4q13.3		610912	"AMTN, AI3B"	Amelotin	AMTN	401138	ENSG00000187689	mutation identified in 1 AI3B family	"?Amelogenesis imperfecta, type IIIB, 617607 (3), Autosomal dominant"	Amtn (MGI:1918671)			
chr4	70592257	70607287	4q21	4q13.3		601259	"AMBN, AI1F"	Ameloblastin	AMBN	258	ENSG00000178522	mutation identified in 1 AI1F family	"Amelogenesis imperfecta, type IF, 616270 (3), Autosomal recessive"	Ambn (MGI:104655)			
chr4	70627470	70646818	4q21	4q13.3		606585	"ENAM, AIH2, AI1C"	Enamelin	ENAM	10117	ENSG00000132464		"Amelogenesis imperfecta, type IB, 104500 (3), Autosomal dominant; Amelogenesis imperfecta, type IC, 204650 (3), Autosomal recessive"	Enam (MGI:1333772)			
chr4	70655540	70666630	4q21	4q13.3		147790	IGJ	"Immunoglobulin J polypeptide, linker protein for"	JCHAIN	3512	ENSG00000132465			Jchain (MGI:96493)			
chr4	70688478	70690550	4q21	4q13.3		611614	"UTP3, CRL1, CRLZ1"	"UTP3, S. crevisiae, homolog of"	UTP3	57050	ENSG00000132467			Utp3 (MGI:1919230)			
chr4	70704203	70808621	4q13.3	4q13.3		611194	"RUFY3, SINGAR1, RIPX"	FUN and FYVE domains-containing protein 3	RUFY3	22902	ENSG00000018189			Rufy3 (MGI:106484)			
chr4	70815781	70843273	4q13	4q13.3		604851	GRSF1	G-rich RNA sequence-binding factor 1	GRSF1	2926	ENSG00000132463			Grsf1 (MGI:106479)			
chr4	70993547	71030913	4q13.3-q21.1	4q13.3		125450	DCK	Deoxycytidine kinase	DCK	1633	ENSG00000156136			Dck (MGI:102726)			
chr4	71062645	71572086	4q21	4q13.3		603345	"SLC4A4, NBC1, KNBC"	"Solute carrier family 4, sodium bicarbonate cotransporter, member 4"	SLC4A4	8671	ENSG00000080493		"Renal tubular acidosis, proximal, with ocular abnormalities, 604278 (3), Autosomal recessive"	Slc4a4 (MGI:1927555)			
chr4	71741692	71805519	4q12	4q13.3		139200	"GC, DBP"	Group-specific component (vitamin D-binding protein)	GC	2638	ENSG00000145321	4q13-q21.1 by in situ hybridization		Gc (MGI:95669)			
chr4	72031803	72148200	4q13.2-q13.3	4q13.3		607449	"GPR74, NPFF2, NPGPR"	G protein-coupled receptor 74	NPFFR2	10886	ENSG00000056291			Npffr2 (MGI:1860130)			
chr4	72280968	72568798	4q21	4q13.3		605011	ADAMTS3	"A Disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 3"	ADAMTS3	9508	ENSG00000156140			Adamts3 (MGI:3045353)			
chr4	73054695	73069776	4q21.1	4q13.3		610428	COX18	Cytochrome c oxidase assembly protein COX18	COX18	285521	ENSG00000163626			Cox18 (MGI:2448532)			
chr4	73073965	73259765	4q13.3	4q13.3		615929	"ANKRD17, GTAR"	Ankyrin repeat domain-containing protein 17	ANKRD17	26057	ENSG00000132466			Ankrd17 (MGI:1932101)			
chr4	73404238	73421483	4q11-q13	4q13.3		103600	"ALB, ANALBA, FDAH"	Albumin	ALB	213	ENSG00000163631	linked to GC	"Analbuminemia, 616000 (3); [Dysalbuminemic hyperthyroxinemia], 615999 (3)"	Alb (MGI:87991)			
chr4	73436218	73455784	4q11-q13	4q13.3		104150	"AFP, HPAFP, AFPD"	Alpha-fetoprotein	AFP	174	ENSG00000081051	order: 5'-ALB-3'--5'-AFP-3'	"Alpha-fetoprotein deficiency, 615969 (3), Autosomal recessive; [Hereditary persistence of alpha-fetoprotein], 615970 (3), Autosomal dominant"	Afp (MGI:87951)			
chr4	73481744	73504000	4q11-q13	4q13.3		104145	"AFM, ALBA, ALB2"	Afamin	AFM	173	ENSG00000079557	10kb 3' of AFP		Afm (MGI:2429409)			
chr4	73571549	73620630	4q13.3	4q13.3		612620	RASSF6	"Ras association domain family, member 6"	RASSF6	166824	ENSG00000169435			Rassf6 (MGI:1920496)			
chr4	73740505	73743715	4q12-q13	4q13.3		146930	IL8	Interleukin-8	CXCL8	3576	ENSG00000169429						
chr4	73836555	73838759	4q12-q13	4q13.3		138965	"CXCL6, SCYB6, GCP2"	"Chemokine, C-X-C motif, ligand 6 (granulocyte chemotactic protein-2)"	CXCL6	6372	ENSG00000124875			Cxcl5 (MGI:1096868)			
chr4	73848735	73849252	4q12-q13	4q13.3		188035	"PPBPL1, TGB2"	"Pro-platelet basic protein-like 1 (thromboglobulin, beta-2)"	PPBPP1	728045		"in cluster with PPBP, PF4, and PF4V1"					
chr4	73853295	73854483	4q12-q13	4q13.3		173461	PF4V1	"Platelet factor 4, variant 1 (PF4-like)"	PF4V1	5197	ENSG00000109272	same region as PF4 and IP10					
chr4	73869391	73871301	4q12-q13	4q13.3		155730	"CXCL1, GRO1, MGSA"	"Chemokine, C-X-C, ligand 1 (GRO1 oncogene; melanoma growth stimulating activity, alpha)"	CXCL1	2919	ENSG00000163739	apparently cluster of 3 GRO genes					
chr4	73980824	73982123	4q12-q13	4q13.3		173460	PF4	Platelet factor 4	PF4	5196	ENSG00000163737	6kb from PF4V1		Pf4 (MGI:1888711)			
chr4	73986438	73988189	4q12-q13	4q13.3		121010	"PPBP, CXCL7, SCYB7, CTAP3, TGB"	Pro-platelet basic protein	PPBP	5473	ENSG00000163736	less than 7kb from PF4					
chr4	73995641	73998728	4q12-q13	4q13.3		600324	"CXCL5, SCYB5, ENA78"	"Chemokine, C-X-C motif, ligand 5 (epithelial-derived neutrophil-activating peptide 78)"	CXCL5	6374	ENSG00000163735						
chr4	74036588	74038772	4q12-q13	4q13.3		139111	"CXCL3, GRO3, MIP2B"	"Chemokine, C-X-C motif, ligand 3 (GRO3 oncogene)"	CXCL3	2921	ENSG00000163734			Cxcl2 (MGI:1340094)			
chr4	74054037	74055398	4q13.3	4q13.3		611591	"PPBPP2, PPBPL2"	Pro-platelet basic protein pseudogene 2	PPBPP2	10895							
chr4	74097034	74099279	4q12-q13	4q13.3		139110	"CXCL2, GRO2, MIP2A"	"Chemokine, C-X-C motif, ligand 2 (GRO2 oncogene)"	CXCL2	2920	ENSG00000081041			Cxcl1 (MGI:108068)			
chr4	74123272	74303098	4q13.3	4q13.3		614047	MTHFD2L	"Methylenetetrahydrofolate dehydrogenase 2-like, NADP(+)-dependent"	MTHFD2L	441024	ENSG00000163738			Mthfd2l (MGI:1915871)			
chr4	74365142	74388759	4q13.3	4q13.3		602061	EREG	Epiregulin	EREG	2069	ENSG00000124882			Ereg (MGI:107508)			
chr4	74445097	74455008	4q13-q21	4q13.3		104640	AREG	Amphiregulin	AREG	374	ENSG00000109321			Areg (MGI:88068)			
chr4	74744758	74794717	4q13-q21	4q13.3		600345	BTC	Betacellulin	BTC	685	ENSG00000174808	tightly linked to Areg in mouse		Btc (MGI:99439)			
chr4	74933074	75050114	4q13.3	4q13.3		617688	"PARM1, CIPAR1"	Prostate androgen-regulated mucin-like protein 1	PARM1	25849	ENSG00000169116			Parm1 (MGI:2443349)			
chr4	75300000	87100000	4q21			613509	"DEL4q21, C4DELq21"	Chromosome 4q21 deletion syndrome				contiguous gene deletion if at least 30 genes	"Chromosome 4q21 deletion syndrome, 613509 (4), Isolated cases"				
chr4	75300000	113200000	4q21-q25			134720	FECB	"Fecundity gene, Boorla, of sheep, homolog of"		7892		sheep chr.6					
chr4	75300000	154600000	4q21-q31			608371	OFC4	Orofacial cleft 4		474387			"Orofacial cleft 4, 608371 (2)"				
chr4	75300000	100100000	4q21-q23			609566	PFM3	Parietal foramina 3	PFM3	619475		maximum lod between D4S2986 and D4S421	"Parietal foramina 3, 609566 (2), Autosomal dominant"				
chr4	75479036	75515056	4q21.1	4q21.1		607680	"RCHY1, ZNF363, PIRH2, ARNIP"	"Ring finger and CHY zinc finger domain containing 1, E3 ubiquitin protein ligase"	RCHY1	25898	ENSG00000163743			Rchy1 (MGI:1915348)			
chr4	75513943	75547333	4q21.1	4q21.1		612535	THAP6	THAP domain-containing protein 6	THAP6	152815	ENSG00000174796						
chr4	75554996	75565892	4q21.1	4q21.1		614829	"ODAPH, C4orf26"	Odontogenesis-associated phosphoprotein	ODAPH	152816	ENSG00000174792		"Amelogenesis imperfecta, type IIA4, 614832 (3), Autosomal recessive"	Odaph (MGI:2685891)			
chr4	75576493	75630539	4q21.1	4q21.1		603442	"CDKL2, KKIAMRE, P56"	Cyclin-dependent kinase-like 2	CDKL2	8999	ENSG00000138769			Cdkl2 (MGI:1858227)			
chr4	75724521	75814288	4q21.1	4q21.1		603344	"USO1, TAP, p115"	"USO1 vesicle docking protein, S. cerevisiae, homolog of"	USO1	8615	ENSG00000138768			Uso1 (MGI:1929095)			
chr4	75859871	75902527	4q21.1	4q21.1		602256	PPEF2	"Protein phosphatase, EF hand calcium-binding domain-2"	PPEF2	5470	ENSG00000156194			Ppef2 (MGI:1342304)			
chr4	75910654	75941012	4q21.1	4q21.1		607469	"NAAA, ASAHL"	N-acylethanolamine acid amidase	NAAA	27163	ENSG00000138744			Naaa (MGI:1914361)			
chr4	76001341	76007522	4q21	4q21.1		601704	"CXCL9, MIG, SCYB9"	"Chemokine, C-X-C motif, ligand 9"	CXCL9	4283	ENSG00000138755	close to INP10					
chr4	76011167	76112801	4q21.1	4q21.1		603086	ART3	ADP-ribosyltransferase 3	ART3	419	ENSG00000156219			Art3 (MGI:1202729)			
chr4	76021115	76023535	4q21	4q21.1		147310	"CXCL10, INP10"	"Chemokine, C-X-C motif, ligand 10 (interferon-inducible cytokine IP-10)"	CXCL10	3627	ENSG00000169245	?involved in monocytic leukemia with t(4;11)(q21;q23)		Cxcl10 (MGI:1352450)			
chr4	76033681	76036196	4q21.2	4q21.1		604852	"CXCL11, SCYB11, IP9, SCYB9B"	"Chemokine, C-X-C motif, ligand 11"	CXCL11	6373	ENSG00000169248						
chr4	76114658	76148514	4q21.1	4q21.1		607607	NUP54	"Nucleoporin, 54kD"	NUP54	53371	ENSG00000138750			Nup54 (MGI:1920460)			
chr4	76158736	76213898	4q13-q21	4q21.1		602257	"SCARB2, CD36L2, LIMPII, AMRF, EPM4"	"Scavenger receptor class B, member 2"	SCARB2	950	ENSG00000138760		"Epilepsy, progressive myoclonic 4, with or without renal failure, 254900 (3), Autosomal recessive"	Scarb2 (MGI:1196458)			
chr4	76306025	76311129	4q25-q34	4q21.1		607406	GENEX3414	Genethonin 1	STBD1	8987	ENSG00000118804			Stbd1 (MGI:1261768)			
chr4	76435099	76783252	4q21.1	4q21.1		604570	"SHROOM3, SHRM, KIAA1481"	Shroom family member 3	SHROOM3	57619	ENSG00000138771			Shroom3 (MGI:1351655)			
chr4	76949713	77040153	4q21.1	4q21.1		612887	11-Sep	Septin 11	11-Sep	55752	ENSG00000138758			Sept11 (MGI:1277214)			
chr4	77157203	77170059	4q21.1	4q21.1		603203	CCNG2	Cyclin G2	CCNG2	901	ENSG00000138764			Ccng2 (MGI:1095734)			
chr4	77511752	77611833	4q21	4q21.1		605149	"CXCL13, SCYB13, BCA1, BLC"	"Chemokine, C-X-C motif, ligand 13"	CXCL13	10563	ENSG00000156234			Cxcl13 (MGI:1888499)			
chr4	77862650	77952789	4q21.1	4q21.1		611821	MRPL1	Mitochondrial ribosomal protein L1	MRPL1	65008	ENSG00000169288			Mrpl1 (MGI:2137202)			
chr4	78056967	78544268	4q21	4q21.21		607830	"FRAS1, FRASRS1"	FRAS1 gene	FRAS1	80144	ENSG00000138759		"Fraser syndrome 1, 219000 (3), Autosomal recessive"	Fras1 (MGI:2385368)			
chr4	78551587	78610450	4q21	4q21.21		106490	"ANXA3, ANX3"	Annexin A3 (lipocortin III)	ANXA3	306	ENSG00000138772			Anxa3 (MGI:1201378)			
chr4	78776377	78916364	4q21.21	4q21.21		617648	"BMP2K, BIKE"	BMP2-inducible kinase	BMP2K	55589	ENSG00000138756			Bmp2k (MGI:2155456)			
chr4	78887224	78939427	4q21.21	4q21.21		614577	"PAQR3, RKTG"	"Progestin and ADIPOQ receptor family, member 3"	PAQR3	152559	ENSG00000163291			Paqr3 (MGI:2679683)			
chr4	79827470	79863246	4q21.1	4q21.21		609717	"PCAT4, GDEP"	Prostate cancer-associated transcript 4	PCAT4	118425							
chr4	79901616	80073471	4q21	4q21.21		608041	"ANTXR2, CMG2, HFS"	Anthrax toxin receptor 2	ANTXR2	118429	ENSG00000163297		"Hyaline fibromatosis syndrome, 228600 (3), Autosomal recessive"	Antxr2 (MGI:1919164)			
chr4	80183417	80204328	4q21.21	4q21.21		616639	"PRDM8, EPM10"	PR domain-containing protein 8	PRDM8	56978	ENSG00000152784	mutation identified in 1 EPM10 family	"?Epilepsy, progressive myoclonic, 10, 616640 (3), Autosomal recessive"	Prdm8 (MGI:1924880)			
chr4	80266587	80291016	4q21	4q21.21		165190	"FGF5, TCMGLY"	Fibroblast growth factor-5	FGF5	2250	ENSG00000138675		"Trichomegaly, 190330 (3), Autosomal recessive"	Fgf5 (MGI:95519)			
chr4	81030777	81057624	4p14-q21	4q21.21		112263	BMP3	Bone morphogenetic protein-3	BMP3	651	ENSG00000152785			Bmp3 (MGI:88179)			
chr4	81086873	81217836	4q13.1-q21.1	4q21.21		601591	"PRKG2, PRKGR2"	"Protein kinase, cGMP-dependent, type II"	PRKG2	5593	ENSG00000138669			Prkg2 (MGI:108173)			
chr4	81426392	81471927	4q12-q21	4q21.21		614532	"RASGEF1B, GPIG4"	"RASGEF domain family, member 1B"	RASGEF1B	153020	ENSG00000138670			Rasgef1b (MGI:2443755)			
chr4	82353313	82373995	4q21.1-q21.2	4q21.22		601324	"HNRPD, AUF1, AUF1A"	Heterogeneous nuclear ribonucleoprotein D	HNRNPD	3184	ENSG00000138668			Hnrnpd (MGI:101947)			
chr4	82422563	82430224	4q21.33	4q21.22		607137	"HNRNPDL, HNRPDL, JKTBP, LGMD1G"	Heterogeneous nuclear ribonucleoprotein D-like protein	HNRNPDL	9987	ENSG00000152795		"Muscular dystrophy, limb-girdle, type 1G, 609115 (3), Autosomal dominant"	Hnrnpdl (MGI:1355299)			
chr4	82483169	82562559	4q21.22	4q21.22		617292	"TMEM150C, TTN3"	Transmembrane protein 150C	TMEM150C	441027	ENSG00000249242			Tmem150c (MGI:3041258)			
chr4	82629536	82798856	4q21.1	4q21.22		608370	"SCD4, ACOD4"	Stearoyl-CoA desaturase 4	SCD5	79966	ENSG00000145284						
chr4	82818508	82900570	4q21.22	4q21.22		610257	"SEC31A, SEC31L1, KIAA0905"	"Sec31, yeast, homolog of, A"	SEC31A	22872	ENSG00000138674			Sec31a (MGI:1916412)			
chr4	82900649	82920282	4q21.22	4q21.22		612537	THAP9	THAP domain-containing protein 9	THAP9	79725	ENSG00000168152						
chr4	82924602	83012950	4q21.22	4q21.22		613367	LIN54	"Lin54, C. elegans, homolog of"	LIN54	132660	ENSG00000189308			Lin54 (MGI:2140902)			
chr4	83035085	83075817	4q21.22	4q21.22		616008	"COPS4, CSN4"	"COP9 signalosome, subunit 4"	COPS4	51138	ENSG00000138663			Cops4 (MGI:1349414)			
chr4	83090047	83114757	4q21	4q21.22		607515	PLAC8	Placenta-specific gene 8	PLAC8	51316	ENSG00000145287			Plac8 (MGI:2445289)			
chr4	83138563	83285133	4q21-q22	4q21.22-q21.23		609825	"COQ2, COQ10D1, MSA1"	"CoQ2, S. cerevisiae, homolog of (parahydroxybenzoate-polyprenyltransferase, mitochondrial)"	COQ2	27235	ENSG00000173085		"Coenzyme Q10 deficiency, primary, 1, 607426 (3), Autosomal recessive; {Multiple system atrophy, susceptibility to}, 146500 (3), Autosomal recessive, Autosomal dominant"	Coq2 (MGI:1919133)			
chr4	83292460	83335152	4q21.3	4q21.23		604724	"HPSE, HSE1, HPA"	Heparanase	HPSE	10855	ENSG00000173083			Hpse (MGI:1343124)			
chr4	83407342	83456045	4q21.23	4q21.23		606769	"HELQ, HEL308"	"Helicase, POLQ-like"	HELQ	113510	ENSG00000163312			Helq (MGI:2176740)			
chr4	83455931	83461722	4q21.23	4q21.23		611983	"MRPS18C, MRPS18-1"	Mitochondrial ribosomal protein S18C	MRPS18C	51023	ENSG00000163319	6 pseudogenes		Mrps18c (MGI:1915985)			
chr4	83460938	83485177	4q21.2	4q21.23		611143	"FAM175A, CCDC98, ABRAXAS, ABRA1"	"Family with sequence similarity 175, member A"	ABRAXAS1	84142	ENSG00000163322			Abraxas1 (MGI:1917931)			
chr4	83535633	83605874	4q21.23	4q21.23		610958	"AGPAT9, GPAT3, MAG1"	1-acylglycerol-3-phosphate O-acyltransferase 9	GPAT3	84803	ENSG00000138678			Gpat3 (MGI:3603816)			
chr4	84493282	84498233	4q21.2-q22	4q21.23		602563	"NKX6-1, NKX6A"	"NK6, Drosophila, homolog of, 1"	NKX6-1	4825	ENSG00000163623			Nkx6-1 (MGI:1206039)			
chr4	84582903	84651339	4q21	4q21.23		603548	CDS1	CDP-diacylglycerol synthase 1	CDS1	1040	ENSG00000163624			Cds1 (MGI:1921846)			
chr4	84669536	84966390	4q21	4q21.23		617485	"WDFY3, ALFY, BCHS, MCPH18"	WD repeat- and FYVE domain-containing protein 3	WDFY3	23001	ENSG00000163625	mutation identified in 1 MCPH18 family	"?Microcephaly 18, primary, autosomal dominant, 617520 (3), Autosomal dominant"	Wdfy3 (MGI:1096875)			
chr4	85475130	86002669	4q21	4q21.2-q21.3		610586	"ARHGAP24, RCGAP72, FILGAP"	RHO GTPase-activating protein 24	ARHGAP24	83478	ENSG00000138639			Arhgap24 (MGI:1922647)			
chr4	86012295	86594624	4q21.3	4q21.3		602897	"MAPK10, PRKM10, JNK3"	Mitogen-activated protein kinase 10	MAPK10	5602	ENSG00000109339			Mapk10 (MGI:1346863)			
chr4	86594306	86815175	4q21.3	4q21.3		600267	PTPN13	"Protein tyrosine phosphatase, nonreceptor-type, 13 (APO-1/CD95 (Fas)-associated phosphatase)"	PTPN13	5783	ENSG00000163629	633bp upstream of JNK3		Ptpn13 (MGI:103293)			
chr4	86823467	86849262	4q21.3	4q21.3		613366	"SLC10A6, SOAT"	"Solute carrier family 10 (sodium/bile acid cotransporter family), member 6"	SLC10A6	345274	ENSG00000145283			Slc10a6 (MGI:1923000)			
chr4	86934605	87141053	4q21	4q21.3-q22.1		159557	"AFF1, MLLT2, AF4"	"AF4/FMR2 family, member 1"	AFF1	4299	ENSG00000172493	fuses with ALL1		Aff1 (MGI:1100819)			
chr4	87100000	92800000	4q22.1			613518	ATOD8	"Dermatitis, atopic, 8"		105463125			"{Dermatitis, atopic, susceptibility to, 8}, 613518 (2)"				
chr4	87100000	97900000	4q22			612343	MUSQTL1	Musical aptitude quantitative trait locus 1		100192307		near D4S423 and D4S2460	"[Musical aptitude QTL 1], 612343 (2)"				
chr4	87100000	122800000	4q22-q27			609994	MYP11	Myopia 11	MYP11	594832		max lod at D4S1564	"Myopia 11, 609994 (2)"				
chr4	87160102	87220607	4q22.1	4q22.1		611967	"KLHL8, KIAA1378"	Kelch-like 8	KLHL8	57563	ENSG00000145332			Klhl8 (MGI:2179430)			
chr4	87303788	87322905	4q22.1	4q22.1		612127	"HSD17B13, SCDR9"	17-beta-hydroxysteroid dehydrogenase XIII	HSD17B13	345275	ENSG00000170509			Hsd17b13 (MGI:2140804)			
chr4	87336521	87391302	4q21	4q22.1		612831	"HSD17B11, RETSDR2, PAN1B"	17-beta-hydroxysteroid dehydrogenase XI	HSD17B11	51170	ENSG00000198189			Hsd17b11 (MGI:2149821)			
chr4	87608528	87616872	4q21.3	4q22.1		125485	"DSPP, DPP, DGI1, DFNA39, DTDP2"	Dentin sialophosphoprotein	DSPP	1834	ENSG00000152591		"Deafness, autosomal dominant 39, with dentinogenesis, 605594 (3), Autosomal dominant; Dentin dysplasia, type II, 125420 (3), Autosomal dominant; Dentinogenesis imperfecta, Shields type II, 125490 (3), Autosomal dominant; Dentinogenesis imperfecta, Shields type III, 125500 (3), Autosomal dominant"				
chr4	87650301	87664360	4q21	4q22.1		600980	"DMP1, ARHR, ARHP"	Dentin matrix acidic phosphoprotein	DMP1	1758	ENSG00000152592		"Hypophosphatemic rickets, AR, 241520 (3), Autosomal recessive"	Dmp1 (MGI:94910)			
chr4	87799549	87812448	4q21-q25	4q22.1		147563	IBSP	Integrin-binding sialoprotein (bone sialoprotein II)	IBSP	3381	ENSG00000029559			Ibsp (MGI:96389)			
chr4	87821397	87846816	4q21.1	4q22.1		605912	MEPE	"Matrix, extracellular, phosphoglycoprotein"	MEPE	56955	ENSG00000152595			Mepe (MGI:2137384)			
chr4	87975649	87983410	4q21-q25	4q22.1		166490	"SPP1, OPN"	"Secreted phosphoprotein-1 (osteopontin, bone sialoprotein)"	SPP1	6696	ENSG00000118785			Spp1 (MGI:98389)			
chr4	88007646	88077778	4q21-q23	4q22.1		173910	PKD2	Polycystin-2	PKD2	5311	ENSG00000118762		"Polycystic kidney disease 2, 613095 (3), Autosomal dominant"	Pkd2 (MGI:1099818)			
chr4	88090263	88231625	4q22	4q22.1		603756	"ABCG2, BCRP, ABCP, UAQTL1, GOUT1"	"ATP-binding cassette, subfamily G, member 2"	ABCG2	9429	ENSG00000118777		"[Junior blood group system], 614490 (3); [Uric acid concentration, serum, QTL1], 138900 (3), ?Autosomal dominant"	Abcg2 (MGI:1347061)			
chr4	88257608	88284830	4q22.1	4q22.1		611065	"PPM1K, PP2CM, PTMP, MSUDMV"	"Protein phosphatase, PP2C domain-containing, 1K"	PPM1K	152926	ENSG00000163644	mutation identified in 1 MSUDMV family	"?Maple syrup urine disease, mild variant, 615135 (3)"	Ppm1k (MGI:2442111)			
chr4	88456603	88506169	4q22.2-q22.3	4q22.1		608242	"HERC5, CEB1"	HECT domain and RCC1-like domain 5	HERC5	51191	ENSG00000138646						
chr4	88520977	88523800	4q22.1	4q22.1		610662	"PIGY, HPMRS6"	"Phosphatidylinositol glycan, class Y"	PIGY	84992	ENSG00000255072		"Hyperphosphatasia with mental retardation syndrome 6, 616809 (3), Autosomal recessive"	Pigyl (MGI:1913518)			
chr4	88592422	88709302	4q22.1	4q22.1		605200	HERC3	HECT domain and RCC1-like domain 3	HERC3	8916	ENSG00000138641			Herc3 (MGI:1921248)			
chr4	88695912	88698234	4q21-q22	4q22.1		612203	"NAP1L5, DRLM"	Nucleosome assembly protein 1-like 5	NAP1L5	266812	ENSG00000177432			Nap1l5 (MGI:1923555)			
chr4	88709788	88730102	4q22.1	4q22.1		613300	"FAM13AOS, FAM13A1OS"	FAM13A opposite strand	FAM13A-AS1	285512		overlaps with FAM13A					
chr4	88725953	89111397	4q22.1	4q22.1		613299	"FAM13A, FAM13A1, KIAA0914"	"Family with sequence similarity 13, member A"	FAM13A	10144	ENSG00000138640	overlaps with FAM13AOS					
chr4	89112816	89114900	4q22.1	4q22.1		612973	TIGD2	TIGGER transposable element-derived gene 2	TIGD2	166815	ENSG00000180346			Tigd2 (MGI:1915390)			
chr4	89237665	89308009	4q22.1	4q22.1		611241	"GPRIN3, GRIN3"	G protein-regulated inducer of neurite outgrowth 3	GPRIN3	285513	ENSG00000185477			Gprin3 (MGI:1924785)			
chr4	89724098	89838323	4q21	4q22.1		163890	"SNCA, NACP, PARK1, PARK4"	"Synuclein, alpha (non A4 component of amyloid precursor)"	SNCA	6622	ENSG00000145335		"Dementia, Lewy body, 127750 (3), Autosomal dominant; Parkinson disease 1, 168601 (3), Autosomal dominant; Parkinson disease 4, 605543 (3), Autosomal dominant"	Snca (MGI:1277151)			
chr4	89879538	89954628	4q22.1	4q22.1		601456	"MMRN1, ECM"	Multimerin 1	MMRN1	22915	ENSG00000138722			Mmrn1 (MGI:1918195)			
chr4	92303621	93810414	4q22	4q22.1-q22.2		602368	"GRID2, SCAR18"	"Glutamate receptor, ionotropic, delta-2"	GRID2	2895	ENSG00000152208		"Spinocerebellar ataxia, autosomal recessive 18, 616204 (3), Autosomal recessive"	Grid2 (MGI:95813)			
chr4	93828926	93829990	4q22	4q22.2		601461	"ATOH1, ATH1"	"Atonal, Drosophila, homolog of, 1"	ATOH1	474	ENSG00000172238			Atoh1 (MGI:104654)			
chr4	94207607	94291291	4q22-q23	4q22.3		612761	"SMARCAD1, KIAA1122, ETL1, HEL1, ADERM, BASNS"	"SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily A, DEAD/H box-containing, 1"	SMARCAD1	56916	ENSG00000163104		"Adermatoglyphia, 136000 (3), Autosomal dominant; Basan syndrome, 129200 (3), Autosomal dominant"	Smarcad1 (MGI:95453)			
chr4	94298555	94342875	4q21-q22	4q22.3		602598	"HPGDS, PGDS"	"Prostaglandin D2 synthase, hematopoietic"	HPGDS	27306	ENSG00000163106			Hpgds (MGI:1859384)			
chr4	94451856	94668226	4q22	4q22.3		605904	ENH	Enigma-like LIM domain protein	PDLIM5	10611	ENSG00000163110			Pdlim5 (MGI:1927489)			
chr4	94757976	95158452	4q23-q24	4q22.3		603248	"BMPR1B, ALK6, AMDD, BDA2, BDA1D"	"Bone morphogenetic protein receptor, type IB"	BMPR1B	658	ENSG00000138696		"Acromesomelic dysplasia, Demirhan type, 609441 (3), Autosomal recessive; Brachydactyly, type A1, D, 616849 (3), Autosomal dominant; Brachydactyly, type A2, 112600 (3), Autosomal dominant"	Bmpr1b (MGI:107191)			
chr4	95162503	95549209	4q21-q23	4q22.3		603610	"UNC5C, UNC5H3"	"UNC5, C. elegans, homolog of, C"	UNC5C	8633	ENSG00000182168			Unc5c (MGI:1095412)			
chr4	95840087	95841473	4q22-q23	4q22.3		179061	PDHA2	"Pyruvate dehydrogenase, E1-alpha polypeptide, testis specific form"	PDHA2	5161	ENSG00000163114						
chr4	97900000	100100000	4q23			617478	DNAJB14	"DNAJ/HSP40 homolog, subfamily B, member 14"									
chr4	97900000	100100000	4q23			181600	"TYS, HRZ"	Sclerotylosis	TYS	7303			"Huriez syndrome, 181600 (2), Autosomal dominant"				
chr4	98261375	98443860	4q21-q25	4q23		179502	RAP1GDS1	"RAP1, GTP-GDP dissociation stimulator 1"	RAP1GDS1	5910	ENSG00000138698	fusion partner with NUP98 in ALL	"Lymphocytic leukemia, acute T-cell (3)"	Rap1gds1 (MGI:2385189)			
chr4	98470366	98658660	4q23	4q23		613136	"TSPAN5, NET4"	Tetraspanin 5	TSPAN5	10098	ENSG00000168785			Tspan5 (MGI:1928096)			
chr4	98871683	98930636	4q21-q25	4q23		133440	"EIF4E, EIF4EL1, AUTS19"	Eukaryotic translation initiation factor 4E	EIF4E	1977	ENSG00000151247	pseudogene on 20	"{Autism, susceptibility to, 19}, 615091 (3)"	Eif4e (MGI:95305)			
chr4	98995636	99063108	4q23	4q23		610151	"METAP1, KIAA0094"	Methionyl aminopeptidase 1	METAP1	23173	ENSG00000164024			Metap1 (MGI:1922874)			
chr4	99070977	99088787	4q21-q25	4q23		103710	"ADH5, FDH"	"Alcohol dehydrogenase (class III), chi polypeptide"	ADH5	128	ENSG00000197894			Adh5 (MGI:87929)			
chr4	99123656	99144297	4q22	4q23		103740	ADH4	"Alcohol dehydrogenase (class II), pi polypeptide"	ADH4	127	ENSG00000198099			Adh4 (MGI:1349472)			
chr4	99202637	99219245	4q23-q24	4q23		103735	ADH6	Alcohol dehydrogenase 6 (aldehyde reductase)	ADH6	130	ENSG00000172955						
chr4	99276365	99291027	4q22	4q23		103700	"ADH1A, ADH1"	"Alcohol dehydrogenase IA (class I), alpha polypeptide"	ADH1A	124	ENSG00000187758						
chr4	99306386	99321441	4q22	4q23		103720	"ADH1B, ADH2"	"Alcohol dehydrogenase IB (class I), beta polypeptide"	ADH1B	125	ENSG00000196616		"{Aerodigestive tract cancer, squamous cell, alcohol-related, protection against} (3); {Alcohol dependence, protection against}, 103780 (3), Multifactorial"				
chr4	99336491	99353044	4q22	4q23		103730	"ADH1C, ADH3"	"Alcohol dehydrogenase IC (class I), gamma polypeptide"	ADH1C	126	ENSG00000248144		"{Alcohol dependence, protection against}, 103780 (3), Multifactorial; {Parkinson disease, susceptibility to}, 168600 (3), Isolated cases, Multifactorial"	Adh1 (MGI:87921)			
chr4	99412260	99435509	4q23-q24	4q23		600086	ADH7	Alcohol dehydrogenase-7	ADH7	131	ENSG00000196344			Adh7 (MGI:87926)			
chr4	99546706	99564056	4q23	4q23		616013	"TRMT10A, RG9MTD2, MSSGM1"	"tRNA methyltransferase 10, S. cerevisiae, homolog of, A"	TRMT10A	93587	ENSG00000145331		"Microcephaly, short stature, and impaired glucose metabolism 1, 616033 (3), Autosomal recessive"	Trmt10a (MGI:1920421)			
chr4	99564077	99623996	4q22-q24	4q23		157147	MTP	"Microsomal triglyceride transfer protein, 88kD"	MTTP	4547	ENSG00000138823		"Abetalipoproteinemia, 200100 (3), Autosomal recessive; {Metabolic syndrome, protection against}, 605552 (3), Autosomal dominant"	Mttp (MGI:106926)			
chr4	99636528	99657805	4q23	4q23		617881	"C4orf54, LOC285556, FOPV"	Chromosome 4 open reading frame 54	C4orf54	285556	ENSG00000248713			1110002E22Rik (MGI:1915066)			
chr4	99816823	99872289	4q25-q27	4q23		605768	"DAPP1, BAM32"	Dual adaptor of phosphotyrosine and 3-phosphoinositides 1	DAPP1	27071	ENSG00000070190			Dapp1 (MGI:1347063)			
chr4	99878337	99894545	4q23	4q23		603296	"LAMTOR3, MP1, MAPBP"	"Late endosomal/lysosomal adaptor, mitogen-activated protein kinase and mammalian target of rapamycin activator 3"	LAMTOR3	8649	ENSG00000109270			Lamtor3 (MGI:1929467)			
chr4	99948086	99950354	4q24	4q23		142763	H2AZ	H2AZ histone	H2AFZ	3015	ENSG00000164032			H2afz (MGI:1888388)			
chr4	100100000	138500000	4q24-q28			613340	HWE2	"Epilepsy, hot water, 2"		100415904		between D4S1572 and D4S2277	"Epilepsy, hot water, 2, 613340 (2)"				
chr4	100100000	106700000	4q24			157300	"MGR1, MA"	"Migraine with or without aura, susceptibility to, 1"		192115			"{Migraine with or without aura, susceptibility to, 1}, 157300 (2), Autosomal dominant"				
chr4	100100000	106700000	4q24			615312	OCA5	"Albinism, oculocutaneous, type V"	OCA5	101926885		max lod at D4S961	"Albinism, oculocutaneous, type V, 615312 (2), Autosomal recessive"				
chr4	100185869	100190497	4q24-q25	4q24		607730	"DDIT4L, REDD2"	DNA damage-inducible transcript 4-like	DDIT4L	115265	ENSG00000145358			Ddit4l (MGI:1920534)			
chr4	101023429	101348294	4q24-q25	4q24		114105	"PPP3CA, PPP2B, CALNA, CNA1, IECEE1"	"Protein phosphatase-3 (formerly 2B), catalytic subunit, alpha isoform (calcineurin A alpha)"	PPP3CA	5530	ENSG00000138814		"Epileptic encephalopathy, infantile or early childhood, 1, 617711 (3), Autosomal dominant"	Ppp3ca (MGI:107164)			
chr4	101790481	102074811	4q22-q24	4q24		610292	"BANK1, FLJ20706, BANK"	B-cell scaffold protein with ankyrin repeats 1	BANK1	55024	ENSG00000153064			Bank1 (MGI:2442120)			
chr4	102251040	102345497	4q22-q24	4q24		608732	"SLC39A8, BIGM103, CDG2N"	"Solute carrier family 39 (zinc transporter), member 8"	SLC39A8	64116	ENSG00000138821		"Congenital disorder of glycosylation, type IIn, 616721 (3), Autosomal recessive"	Slc39a8 (MGI:1914797)			
chr4	102501265	102617301	4q23-q24	4q24		164011	"NFKB1, CVID12"	Nuclear factor of kappa light chain gene enhancer in B-cells 1 (p105)	NFKB1	4790	ENSG00000109320		"Immunodeficiency, common variable, 12, 616576 (3), Autosomal dominant"	Nfkb1 (MGI:97312)			
chr4	102631485	102760993	4q22-q25	4q24		609489	"MANBA, MANB1"	"Mannosidase, beta A, lysosomal"	MANBA	4126	ENSG00000109323	linked in mouse to Adl-3	"Mannosidosis, beta, 248510 (3), Autosomal recessive"	Manba (MGI:88175)			
chr4	102794382	102868892	4q24	4q24		602963	"UBE2D3, UBCH5C"	Ubiquitin-conjugating enzyme E2D 3	UBE2D3	7323	ENSG00000109332			Ube2d3 (MGI:1913355)			
chr4	102868977	102892806	4q22-q24	4q24		611507	"CISD2, WFS2, ZCD2, ERIS"	CDGSH iron sulfur domain protein 2	CISD2	493856	ENSG00000145354		"Wolfram syndrome 2, 604928 (3), Autosomal recessive"	Cisd2 (MGI:1914256)			
chr4	102885047	103019738	4q24	4q24		611527	NHEDC1	Na+/H+ exchanger domain-containing protein 1	SLC9B1	150159	ENSG00000164037			Slc9b1 (MGI:1921696)			
chr4	103018032	103077370	4q24	4q24		611789	"NHEDC2, NHA2"	NA+/H+ exchanger domain-containing protein 2	SLC9B2	133308	ENSG00000164038			Slc9b2 (MGI:2140077)			
chr4	103105805	103198408	4q24-q25	4q24		117143	"CENPE, MCPH13"	"Centromere autoantigen E, 312kD"	CENPE	1062	ENSG00000138778	mutation identified in 1 MCPH13 family	"?Microcephaly 13, primary, autosomal recessive, 616051 (3), Autosomal recessive"	Cenpe (MGI:1098230)			
chr4	103589467	103719815	4q25	4q24		162332	"TACR3, NK3R, HH11"	Tachykinin receptor 3	TACR3	6870	ENSG00000169836		"Hypogonadotropic hypogonadism 11 with or without anosmia, 614840 (3), Autosomal recessive"	Tacr3 (MGI:892968)			
chr4	104468305	104494966	4q22-q24	4q24		611645	"CXXC4, IDAX"	CXXC finger protein 4	CXXC4	80319	ENSG00000168772			Cxxc4 (MGI:2442112)			
chr4	105145874	105279802	4q24	4q24		612839	"TET2, KIAA1546, MDS"	"TET oncogene family, member 2"	TET2	54790	ENSG00000168769		"Myelodysplastic syndrome, somatic, 614286 (3)"	Tet2 (MGI:2443298)			
chr4	105369076	105474069	4q25	4q24		609988	"PPA2, SCFI, SCFAI"	"Pyrophosphatase, inorganic, 2"	PPA2	27068	ENSG00000138777	mutation identified in 1 SCFAI family	"?Sudden cardiac failure, alcohol-induced, 617223 (3), Autosomal recessive; Sudden cardiac failure, infantile, 617222 (3), Autosomal recessive"	Ppa2 (MGI:1922026)			
chr4	105682626	105708724	4q24	4q24		611355	"INTS12, INT12"	Integrator complex subunit 12	INTS12	57117	ENSG00000138785			Ints12 (MGI:1919043)			
chr4	105708777	105847725	4q24	4q24		615912	GSTCD	Glutathione S-transferase C-terminal domain-containing protein	GSTCD	79807	ENSG00000138780			Gstcd (MGI:1914803)			
chr4	105895439	105971670	4q24	4q24		610306	"NPNT, POEM"	Nephronectin	NPNT	255743	ENSG00000168743			Npnt (MGI:2148811)			
chr4	106041599	106316703	4q24	4q24		616899	"TBCK, IHPRF3"	TBC1 domain-containing kinase	TBCK	93627	ENSG00000145348		"Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, 616900 (3), Autosomal recessive"	Tbck (MGI:2445052)			
chr4	106315609	106349224	4q24	4q24		603605	"AIMP1, SCYE1, EMAP2, EMAPII, HLD3"	ARS-interacting multifunctional protein 1	AIMP1	9255	ENSG00000164022		"Leukodystrophy, hypomyelinating, 3, 260600 (3), Autosomal recessive"	Aimp1 (MGI:102774)			
chr4	106700000	113200000	4q25			611494	ATFB5	"Atrial fibrillation, familial, 5"		100188842		association with rs2200733 and rs10033464	"{Atrial fibrillation, familial, 5}, 611494 (2)"				
chr4	106700000	113200000	4q25			152430	LGV1	"Longevity 1, QTL"		140802		maximum lod at D4S1564	"[Longevity 1], 152430 (2)"				
chr4	107613665	107720262	4q24	4q25		603262	"PAPSS1, ATPSK1"	3'-phosphoadenosine 5'-phosphosulfate synthase 1 (ATP sulfurylase/APS kinase-1)	PAPSS1	9061	ENSG00000138801			Papss1 (MGI:1330587)			
chr4	107823644	107915046	4q25	4q25		611574	"SGMS2, SMS2"	Sphingomyelin synthase 2	SGMS2	166929	ENSG00000164023			Sgms2 (MGI:1921692)			
chr4	107931548	107953460	4q25	4q25		610670	"CYP2U1, SPG56"	"Cytochrome P450, family 2, subfamily U, polypeptide 1"	CYP2U1	113612	ENSG00000155016		"Spastic paraplegia 56, autosomal recessive, 615030 (3), Autosomal recessive"	Cyp2u1 (MGI:1918769)			
chr4	107989713	108035174	4q22-q26	4q25		601609	"HADHSC, SCHAD, HHF4"	"L-3-hydroxyacyl-CoA dehydrogenase, short chain"	HADH	3033	ENSG00000138796		"3-hydroxyacyl-CoA dehydrogenase deficiency, 231530 (3), Autosomal recessive; Hyperinsulinemic hypoglycemia, familial, 4, 609975 (3), Autosomal recessive"	Hadh (MGI:96009)			
chr4	108047544	108168955	4q23-q25	4q25		153245	LEF1	Lymphoid enhancer-binding factor-1	LEF1	51176	ENSG00000138795		"Sebaceous tumors, somatic (3)"	Lef1 (MGI:96770)			
chr4	108620557	108630483	4q25	4q25		616862	RPL34	Ribosomal protein L34	RPL34	6164	ENSG00000109475			Rpl34-ps2 (MGI:3648994)			
chr4	108742039	108763078	4q25	4q25		614682	AGXT2L1	Alanine-glyoxylate aminotransferase 2-like 1	ETNPPL	64850	ENSG00000164089			Etnppl (MGI:1919010)			
chr4	108808724	109302736	4q25	4q25		610004	"COL25A1, CLAC, CFEOM5"	"Collagen, type XXV, alpha-1 polypeptide"	COL25A1	84570	ENSG00000188517		"Fibrosis of extraocular muscles, congenital, 5, 616219 (3), Autosomal recessive"	Col25a1 (MGI:1924268)			
chr4	109433714	109540458	4q25	4q25		607184	SEC24B	"Sec24-related gene family, member B"	SEC24B	10427	ENSG00000138802			Sec24b (MGI:2139764)			
chr4	109688628	109703472	4q25-q25	4q25		601532	"CASP6, MCH2"	"Caspase 6, apoptosis-related cysteine protease"	CASP6	839	ENSG00000138794			Casp6 (MGI:1312921)			
chr4	109709988	109730085	4q25	4q25		611652	"PLA2G12A, GXII, ROSSY"	"Phospholipase A2, Group XIIA"	PLA2G12A	81579	ENSG00000123739			Pla2g12a (MGI:1913600)			
chr4	109731220	109802224	4q25	4q25		217030	"CFI, FI, AHUS3, ARMD13"	Complement factor I	CFI	3426	ENSG00000205403	40kb distal to EGF	"Complement factor I deficiency, 610984 (3), Autosomal recessive; {Hemolytic uremic syndrome, atypical, susceptibility to, 3}, 612923 (3), Autosomal dominant; {Macular degeneration, age-related, 13, susceptibility to}, 615439 (3), Autosomal dominant"	Cfi (MGI:105937)			
chr4	109815509	109824736	4q25	4q25		606468	"NOLA1, GAR1"	"Nucleolar protein family A, member 1"	GAR1	54433	ENSG00000109534						
chr4	109827993	109844706	4q	4q25		605224	RRH	"Rhodopsin homolog, retinal pigment epithelium-derived (peropsin)"	RRH	10692	ENSG00000180245			Rrh (MGI:1097709)			
chr4	109848181	109872314	4q25	4q25		615004	"LRIT3, FIGLER4, CSNB1F"	"Leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein 3"	LRIT3	345193	ENSG00000183423		"Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058 (3), Autosomal recessive"	Lrit3 (MGI:2685267)			
chr4	109912882	110013078	4q25	4q25		131530	"EGF, URG, HOMG4"	Epidermal growth factor (urogastrone)	EGF	1950	ENSG00000138798	linked to ADH3; cen-ADH3-EGF-IL2-qter	"Hypomagnesemia 4, renal, 611718 (3)"	Egf (MGI:95290)			
chr4	110045850	110199198	4q25	4q25		611546	"ELOVL6, LCE, FACE"	Elongation of very long chain fatty acids-like 6	ELOVL6	79071	ENSG00000170522			Elovl6 (MGI:2156528)			
chr4	110476072	110563336	4q25	4q25		138297	ENPEP	Glutamyl aminopeptidase (aminopeptidase A)	ENPEP	2028	ENSG00000138792			Enpep (MGI:106645)			
chr4	110595512	110615457	4q25	4q25		617286	PANCR	PITX2 adjacent noncoding RNA	PANCR	110231149							
chr4	110617422	110642122	4q25-q26	4q25		601542	"PITX2, IDG2, RIEG1, RGS, IGDS2, ASGD4"	Paired-like homeodomain transcription factor-2	PITX2	5308	ENSG00000164093		"Anterior segment dysgenesis 4, 137600 (3), Autosomal dominant; Axenfeld-Rieger syndrome, type 1, 180500 (3), Autosomal dominant; Ring dermoid of cornea, 180550 (3), Autosomal dominant"	Pitx2 (MGI:109340)			
chr4	110860581	110860646	4q25	4q25		615520	MIR297	Micro RNA 297	MIR297	100126354							
chr4	112231738	112273109	4q25	4q25		610851	"C4orf16, GBAR, 2C18"	Gamma-1 adaptin brefeldin-A resistance protein	AP1AR	55435	ENSG00000138660			Ap1ar (MGI:2384822)			
chr4	112275625	112285902	4q25	4q25		609028	"TIFA, T2BP"	TRAF-interacting protein with forkhead-associated domain	TIFA	92610	ENSG00000145365			Tifa (MGI:2182965)			
chr4	112285994	112442617	4q25	4q25		607347	"ALPK1, LAK, KIAA1527"	Alpha-kinase 1	ALPK1	80216	ENSG00000073331			Alpk1 (MGI:1918731)			
chr4	112513515	112516171	4q25	4q25		606624	"NEUROG2, NGN2, ATOH4"	Neurogenin 2	NEUROG2	63973	ENSG00000178403			Neurog2 (MGI:109619)			
chr4	112636963	112657591	4q25	4q25		612026	"LARP7, PIP7S, ALAZS"	"La ribonucleoprotein domain family, member 7"	LARP7	51574	ENSG00000174720		"Alazami syndrome, 615071 (3), Autosomal recessive"	Larp7 (MGI:107634)			
chr4	112647873	112647940	4q25	4q25		614600	MIR367	Micro RNA 367	MIR367	442912							
chr4	112648003	112648070	4q25	4q25		614599	MIR302D	Micro RNA 302D	MIR302D	442896							
chr4	112648182	112648250	4q25	4q25		614596	MIR302A	Micro RNA 302A	MIR302A	407028							
chr4	112648362	112648429	4q25	4q25		614598	MIR302C	Micro RNA 302C	MIR302C	442895							
chr4	112648484	112648556	4q25	4q25		614597	MIR302B	Micro RNA 302B	MIR302B	442894							
chr4	112706017	113383739	4q25-q27	4q25-q26		106410	"ANK2, LQT4"	"Ankyrin-2, nonerythrocytic"	ANK2	287	ENSG00000145362		"Cardiac arrhythmia, ankyrin-B-related, 600919 (3), Autosomal dominant; Long QT syndrome 4, 600919 (3), Autosomal dominant"				
chr4	113451031	113762176	4q26	4q26		607708	CAMK2D	Calcium/calmodulin-dependent protein kinase II-delta	CAMK2D	817	ENSG00000145349			Camk2d (MGI:1341265)			
chr4	113899928	113980463	4q26	4q26		610010	ARSJ	Arylsulfatase J	ARSJ	79642	ENSG00000180801			Arsj (MGI:2443513)			
chr4	114598401	114687913	4q26	4q26		601291	"UGT8, CGT"	UDP glycosyltransferase 8 (cerebroside synthase)	UGT8	7368	ENSG00000174607			Ugt8a (MGI:109522)			
chr4	114824121	115114132	4q25-q26	4q26		615039	NDST4	N-deacetylase/N-sulfotransferase 4	NDST4	64579	ENSG00000138653			Ndst4 (MGI:1932545)			
chr4	117083553	117085579	4q26	4q26		617505	TRAM1L1	Translocation-associated membrane protein 1-like 1	TRAM1L1	133022	ENSG00000174599			Tram1l1 (MGI:2443503)			
chr4	118280037	118353041	4q25-q26	4q26		606709	"PRSS12, BSSP3, MRT1"	"Protease, serine, 12"	PRSS12	8492	ENSG00000164099		"Mental retardation, autosomal recessive 1, 249500 (3), Autosomal recessive"	Prss12 (MGI:1100881)			
chr4	118685369	118712269	4q26	4q26		616504	"METTL14, KIAA1627"	Methyltransferase-like 14	METTL14	57721	ENSG00000145388			Mettl14 (MGI:2442926)			
chr4	118722822	118838682	4q26	4q26		607186	"SEC24D, KIAA0755, CLCRP2"	"Sec24-related gene family, member D"	SEC24D	9871	ENSG00000150961		"Cole-Carpenter syndrome 2, 616294 (3), Autosomal recessive"	Sec24d (MGI:1916858)			
chr4	119135783	119187788	4q26-q27	4q26		605602	"MYOZ2, CMH16"	Myozenin 2	MYOZ2	51778	ENSG00000172399		"Cardiomyopathy, hypertrophic, 16, 613838 (3), Autosomal dominant"	Myoz2 (MGI:1913063)			
chr4	119212582	119295517	4q26	4q26		617431	"USP53, KIAA1350"	Ubiquitin-specific peptidase 53	USP53	54532	ENSG00000145390			Usp53 (MGI:2139607)			
chr4	119317249	119322160	4q28-q31	4q26		134640	FABP2	"Fatty acid-binding protein, intestinal"	FABP2	2169	ENSG00000145384			Fabp2 (MGI:95478)			
chr4	119494394	119628825	4q26	4q26		603310	PDE5A	Phosphodiesterase 5A	PDE5A	8654	ENSG00000138735			Pde5a (MGI:2651499)			
chr4	119900000	122800000	4q27			611598	"CELIAC6, AIS5"	"Celiac disease, susceptibility to, 6"		100188846			"{Autoimmune disease, susceptibility to, 5}, 611598 (2); {Celiac disease, susceptibility to, 6}, 611598 (2)"				
chr4	119900000	122800000	4q27			612622	IDDM23	"Diabetes mellitus, insulin-dependent, 23"		100271697		associated with rs6534347	"{Diabetes mellitus, insulin-dependent, 23}, 612622 (2)"				
chr4	119900000	130100000	4q27-q28.2			614333	MRT29	"Mental retardation, autosomal recessive 29"		100852393		between rs10518325 and rs10518608	"Mental retardation, autosomal recessive 29, 614333 (2), Autosomal recessive"				
chr4	120059421	120066857	4q27	4q27		601467	MAD2L1	"Mitotic arrest deficient, yeast, homolog-like 1"	MAD2L1	4085	ENSG00000164109	previously mapped to 5q23-q31		Mad2l1 (MGI:1860374)			
chr4	120684905	120922865	4q27	4q27		614161	"PRDM5, BCS2"	PR domain-containing protein 5	PRDM5	11107	ENSG00000138738		"Brittle cornea syndrome 2, 614170 (3), Autosomal recessive"	Prdm5 (MGI:1918029)			
chr4	121029292	121072517	4q27	4q27		616506	"NDNF, C4orf31, NORD"	Neuron-derived neurotrophic factor	NDNF	79625	ENSG00000173376			Ndnf (MGI:1915419)			
chr4	121667996	121696993	4q26-q28	4q27		131230	"ANXA5, ENX2, RPRGL3"	Annexin A5 (endonexin II)	ANXA5	308	ENSG00000164111		"{Pregnancy loss, recurrent, susceptibility to, 3}, 614391 (3), Autosomal dominant"	Anxa5 (MGI:106008)			
chr4	121801316	121817020	4q27	4q27		606180	"EXOSC9, PMSCL1"	Exosome component 9	EXOSC9	5393	ENSG00000123737			Exosc9 (MGI:1355319)			
chr4	121816443	121824000	4q27	4q27		123835	"CCNA, CCN1"	Cyclin A	CCNA2	890	ENSG00000145386			Ccna2 (MGI:108069)			
chr4	121824328	121870496	4q27	4q27		607590	BBS7	BBS7 gene	BBS7	55212	ENSG00000138686		"Bardet-Biedl syndrome 7, 615984 (3), Autosomal recessive"	Bbs7 (MGI:1918742)			
chr4	121875979	121952059	4q27	4q27		602345	"TRPC3, TRP3, SCA41"	"Transient receptor potential cation channel, subfamily C, member 3"	TRPC3	7222	ENSG00000138741	mutation identified in one SCA41 patient	"?Spinocerebellar ataxia 41, 616410 (3), Autosomal dominant"	Trpc3 (MGI:109526)			
chr4	122152332	122362758	4q27	4q27		611565	"KIAA1109, ALKKUCS"	KIAA1109 gene	KIAA1109	84162	ENSG00000138688		"Alkuraya-Kucinskas syndrome, 617822 (3), Autosomal recessive"	4932438A13Rik (MGI:2444631)			
chr4	122378965	122429814	4q27	4q27		614130	"ADAD1, TENR"	"Adenosine deaminase domain-containing protein 1, testis-specific"	ADAD1	132612	ENSG00000164113			Adad1 (MGI:103258)			
chr4	122449478	122456494	4q26-q27	4q27		147680	IL2	Interleukin-2	IL2	3558	ENSG00000109471			Il2 (MGI:96548)			
chr4	122612627	122621056	4q26-q27	4q27		605384	"IL21, CVID11"	Interleukin 21	IL21	59067	ENSG00000138684	mutation identified in 1 CVID11 patient	"?Immunodeficiency, common variable, 11, 615767 (3), Autosomal recessive"	Il21 (MGI:1890474)			
chr4	122700436	122744942	4q27	4q27		610683	"BBS12, FLJ35630, C4orf24"	BBS12 gene	BBS12	166379	ENSG00000181004	1Mb centromeric to BBS	"Bardet-Biedl syndrome 12, 615989 (3), Autosomal recessive"	Bbs12 (MGI:2686651)			
chr4	122800000	154600000	4q28-q31			111800	SF	Stoltzfus blood group		6420		~25cM from MNSs	"[Blood group, Stoltzfus system], 111800 (2)"				
chr4	122826707	122898234	4q25-q27	4q28.1		134920	"FGF2, FGFB"	Fibroblast growth factor-2 (basic)	FGF2	2247	ENSG00000138685	many alternate names		Fgf2 (MGI:95516)			
chr4	122923069	123319449	4q28.1	4q28.1		613940	"SPATA5, SPAF, EHLMRS"	Spermatogenesis-associated protein 5	SPATA5	166378	ENSG00000145375		"Epilepsy, hearing loss, and mental retardation syndrome, 616577 (3), Autosomal recessive"	Spata5 (MGI:1927170)			
chr4	123396790	123403759	4q28.1	4q28.1		602465	SPRY1	"Sprouty, Drosophila, homolog of"	SPRY1	10252	ENSG00000164056			Spry1 (MGI:1345139)			
chr4	125314912	125492931	4q28.1	4q28.1		612411	"FAT4, VMLDS2, HKLLS2"	"FAT tumor suppressor, Drosophila, homolog of, 4"	FAT4	79633	ENSG00000196159		"Hennekam lymphangiectasia-lymphedema syndrome 2, 616006 (3), Autosomal recessive; Van Maldergem syndrome 2, 615546 (3), Autosomal recessive"	Fat4 (MGI:3045256)			
chr4	127623270	127716778	4q28	4q28.1		610621	"INTU, KIAA1284, PDZK6, SRTD20, OFD17"	"Inturned, Drosophila, homolog of"	INTU	27152	ENSG00000164066	mutation identified in 1 SRTD20 patient and 1 OFD17 patient	"?Orofaciodigital syndrome XVII, 617926 (3); ?Short-rib throacic dysplasia 20 with polydactyly, 617925 (3)"	Intu (MGI:2443752)			
chr4	127730371	127774298	4q28.1	4q28.1		610796	"SLC25A31, ANT4, AAC4"	"Solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 31"	SLC25A31	83447	ENSG00000151475			Slc25a31 (MGI:1920583)			
chr4	127880860	127899223	4q27-q28	4q28.1		605031	"PLK4, STK18, SAK, MCCRP2"	Polo-like kinase 4 (serine/threonine protein kinase-18)	PLK4	10733	ENSG00000142731		"Microcephaly and chorioretinopathy, autosomal recessive, 2, 616171 (3), Autosomal recessive"	Plk4 (MGI:101783)			
chr4	127917804	127966031	4q28.1-q28.2	4q28.2		611124	"MFSD8, MGC33302, CLN7, CCMD"	Major facilitator superfamily domain-containing protein 8	MFSD8	256471	ENSG00000164073		"Ceroid lipofuscinosis, neuronal, 7, 610951 (3), Autosomal recessive; Macular dystrophy with central cone involvement, 616170 (3), Autosomal recessive"	Mfsd8 (MGI:1919425)			
chr4	128269236	128288828	4q26	4q28.2		607735	PGRMC2	Progesterone receptor membrane component 2	PGRMC2	10424	ENSG00000164040			Pgrmc2 (MGI:1918054)			
chr4	128809622	128875223	4q28.2	4q28.2		610514	"PHF17, JADE1"	PHD finger protein 17	JADE1	79960	ENSG00000077684			Jade1 (MGI:1925835)			
chr4	128874389	129093606	4q28.2	4q28.2		611399	"SCLT1, CAP1A"	Sodium channel and clathrin linker 1	SCLT1	132320	ENSG00000151466			Sclt1 (MGI:1914411)			
chr4	133149289	133208605	4q28.3	4q28.3		608286	"PCDH10, KIAA1400"	Protocadherin 10	PCDH10	57575	ENSG00000138650			Pcdh10 (MGI:1338042)			
chr4	137518917	137532529	4q31	4q28.3		608287	"PCDH18, KIAA1562"	Protocadherin 18	PCDH18	54510	ENSG00000189184			Pcdh18 (MGI:1920423)			
chr4	138164093	138242348	4q28.3	4q28.3		607933	"SLC7A11, XCT"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 11"	SLC7A11	23657	ENSG00000151012			Slc7a11 (MGI:1347355)			
chr4	138500000	154600000	4q31			609782	AAA2	"Aortic aneurysm, familial abdominal 2"		100505390		max lod at D4S1644	"Aortic aneurysm, familial abdominal 2, 609782 (2)"				
chr4	138500000	154600000	4q31			605428	DFNB26	"Deafness, autosomal recessive 26"	DFNB26	23714			"Deafness, autosomal recessive 26, 605428 (2), Autosomal recessive"				
chr4	138500000	182300000	4q31-q34			609985	PAND3	Panic disorder 3		677663		max lod at D4S413	"Panic disorder 3, 609985 (2)"				
chr4	138500000	182300000	4q31-q34			607857	PSORS9	Psoriasis susceptibility 9	PSORS9	359825		max lod at D4S1597	"{Psoriasis susceptibility 9}, 607857 (2)"				
chr4	138500000	154600000	4q31			612224	STQTL12	Stature quantitative trait locus 12		100301523		associated with rs6854783	"{Stature QTL 12}, 612224 (2)"				
chr4	139015758	139045938	4q31.1	4q31.1		608468	"CCRN4L, CCR4L, CCR4"	Carbon catabolite repression 4-like	NOCT	25819	ENSG00000151014			Noct (MGI:109382)			
chr4	139289916	139302550	4q28.2-q31.1	4q31.1		603844	NDUFC1	"NADH-ubiquinone oxidoreductase 1, subcomplex C1"	NDUFC1	4717	ENSG00000109390			Ndufc1 (MGI:1913627)			
chr4	139301466	139390780	4q31.1	4q31.1		608000	"NAA15, NARG1, NATH, MRD50"	"N-alpha-acetyltransferase 15, NatA auxiliary subunit"	NAA15	80155	ENSG00000164134		"Mental retardation, autosomal dominant 50, 617787 (3), Autosomal dominant"	Naa15 (MGI:1922088)			
chr4	139453231	139475915	4q31.1	4q31.1		605950	"RAB33B, SMC2"	Ras-associated protein RAB33B	RAB33B	83452	ENSG00000172007		"Smith-McCort dysplasia 2, 615222 (3), Autosomal recessive"	Rab33b (MGI:1330805)			
chr4	139495933	139556768	4q31.1	4q31.1		606594	"SETD7, SET7, KIAA1717"	SET domain-containing protein 7	SETD7	80854	ENSG00000145391			Setd7 (MGI:1920501)			
chr4	139665724	139754607	4q28-q31	4q31.1		601733	"MGST2, GST2"	Microsomal glutathione S-transferase 2	MGST2	4258	ENSG00000085871			Mgst2 (MGI:2448481)			
chr4	139716390	140154078	4q28.3	4q31.1		608991	"MAML3, MAM2, KIAA1816"	Mastermind-like 3	MAML3	55534	ENSG00000196782			Maml3 (MGI:2389461)			
chr4	140388452	140427660	4q31.1	4q31.1		601858	CLGN	Calmegin	CLGN	1047	ENSG00000153132			Clgn (MGI:107472)			
chr4	140442256	140499045	4q31.1	4q31.1		610310	LOC152586	LOC152586 gene	MGAT4D	152586	ENSG00000205301			Mgat4d (MGI:1914805)			
chr4	140524145	140553769	4q31.1	4q31.1		610196	ELMOD2	ELMO domain-containing protein 2	ELMOD2	255520	ENSG00000179387			Elmod2 (MGI:2445165)			
chr4	140555769	140568913	4q31	4q31.1		113730	UCP1	"Uncoupling protein 1 (mitochondrial, proton carrier)"	UCP1	7350	ENSG00000109424		"{Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Ucp1 (MGI:98894)			
chr4	141220293	141234696	4q31.1-q31.2	4q31.21		609550	"ZNF330, NOA36"	Zinc finger protein 330	ZNF330	27309	ENSG00000109445			Zfp330 (MGI:1353574)			
chr4	141636595	141733986	4q31	4q31.21		600554	IL15	Interleukin-15	IL15	3600	ENSG00000164136			Il15 (MGI:103014)			
chr4	143336829	143474564	4q13.1	4q31.21		604439	GAB1	Grb2-associated binding protein 1	GAB1	2549	ENSG00000109458			Gab1 (MGI:108088)			
chr4	143513462	143557488	4q31.1-q31.2	4q31.21		603375	"SMARCA5, SNF2H"	"SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 5"	SMARCA5	8467	ENSG00000153147			Smarca5 (MGI:1935129)			
chr4	143577406	143700674	4q31.2	4q31.21		608946	FREM3	FRAS1-related extracellular matrix protein 3	FREM3	166752	ENSG00000183090			Frem3 (MGI:2685641)			
chr4	143870865	143912130	4q28-q31	4q31.21		138590	"GYPE, GPE"	Glycophorin E	GYPE	2996	ENSG00000197465	tandem: 5'-GYPA-GYPB-GYPE-3'; ?4q31.1					
chr4	143995171	144021860	4q28-q31	4q31.21		617923	"GYPB, SS"	Glycophorin B	GYPB	2994	ENSG00000250361		"[Blood group, Ss], 111740 (3); {Malaria, resistance to}, 611162 (3)"				
chr4	144109302	144140853	4q28.2-q31.1	4q31.21		617922	"GYPA, MN, GPA"	Glycophorin A	GYPA	2993	ENSG00000170180		"[Blood group, MNSs system], 111300 (3); {Malaria, resistance to}, 611162 (3)"				
chr4	144645995	144740704	4q28-q32	4q31.21		606178	"HHIP, HIP"	Hedgehog-interacting protein	HHIP	64399	ENSG00000164161			Hhip (MGI:1341847)			
chr4	144967116	145098540	4q31.21	4q31.21		613745	"ANAPC10, DOC1, APC10"	"Anaphase-promoting complex, subunit 10"	ANAPC10	10393	ENSG00000164162			Anapc10 (MGI:1916249)			
chr4	145098003	145129523	4q31	4q31.21		601213	"ABCE1, RNASELI, RNS4I"	"ATP-binding cassette, subfamily E, member 1 (ribonuclease L inhibitor)"	ABCE1	6059	ENSG00000164163			Abce1 (MGI:1195458)			
chr4	145133649	145180018	4q31.2	4q31.21		611744	"OTUD4, KIAA1046, HIN1"	OTD domain-containing protein 4	OTUD4	54726	ENSG00000164164			Otud4 (MGI:1098801)			
chr4	145481305	145559175	4q28	4q31.21		601595	"SMAD1, MADH1, MADR1, BSP1"	"Mothers against decapentaplegic, Drosophila, homolog of, 1"	SMAD1	4086	ENSG00000170365			Smad1 (MGI:109452)			
chr4	145619387	145660034	4q31.1-q31.2	4q31.21		607481	MMAA	MMAA gene	MMAA	166785	ENSG00000151611		"Methylmalonic aciduria, vitamin B12-responsive, 251100 (3), Autosomal recessive"	Mmaa (MGI:1923805)			
chr4	146175682	146204435	4q31.2	4q31.22		607286	LSM6	LSM6 protein	LSM6	11157	ENSG00000164167			Lsm6 (MGI:1925901)			
chr4	146638892	146642470	4q31.2	4q31.22		113725	BRN3B	Brn3b POU domain transcription factor	POU4F2	5458	ENSG00000151615			Pou4f2 (MGI:102524)			
chr4	147480916	147544953	4q31.2	4q31.22-q31.23		131243	"EDNRA, MFDA"	Endothelin receptor type A	EDNRA	1909	ENSG00000151617		"Mandibulofacial dysostosis with alopecia, 616367 (3), Autosomal dominant; {Migraine, resistance to}, 157300 (3), Autosomal dominant"	Ednra (MGI:105923)			
chr4	147617370	147637272	4q31.21	4q31.23		613937	"TMEM184C, TMEM34"	Transmembrane protein 184C	TMEM184C	55751	ENSG00000164168			Tmem184c (MGI:2384562)			
chr4	147635649	147684229	4q31.23	4q31.23		616125	"PRMT9, PRMT10"	Protein arginine methyltransferase 9	PRMT9	90826	ENSG00000164169			Prmt9 (MGI:2142651)			
chr4	147732062	148072780	4q31.2	4q31.23		609746	"ARHGAP10, GRAF2, PSGAP"	RHO GTPase-activating protein 10	ARHGAP10	79658	ENSG00000071205			Arhgap10 (MGI:1925764)			
chr4	148078763	148444697	4q31.1	4q31.23		600983	"NR3C2, MLR, MCR"	"Nuclear receptor subfamily 3, group C, member 2 (mineralocorticoid receptor; aldosterone receptor)"	NR3C2	4306	ENSG00000151623		"Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy, 605115 (3); Pseudohypoaldosteronism type I, autosomal dominant, 177735 (3), Autosomal dominant"	Nr3c2 (MGI:99459)			
chr4	150078273	150257456	4q31.23	4q31.2-q31.3		613166	"DCLK2, DCK2, CLIK2, CL2"	Doublecortin-like kinase 2	DCLK2	166614	ENSG00000170390			Dclk2 (MGI:1918012)			
chr4	150200000	169200000	4q31.3-q32.3			611644	HSCR9	"Hirschsprung disease, susceptibility to, 9"		100188850		between D4S3049 and D4S1566	"{Hirschsprung disease, susceptibility to, 9}, 611644 (2)"				
chr4	150264514	151015726	4q31.3	4q31.3		606453	"LRBA, LBA, CDC4L, CVID8"	"Lipopolysaccharide-responsive, beige-like anchor protein"	LRBA	987	ENSG00000198589		"Immunodeficiency, common variable, 8, with autoimmunity, 614700 (3), Autosomal recessive"	Lrba (MGI:1933162)			
chr4	150581924	150584692	4q31.3	4q31.3		604357	"MAB21L2, MCSKS14"	"MAB21, C. elegans, homolog-like 2"	MAB21L2	10586	ENSG00000181541		"Microphthalmia/coloboma and skeletal dysplasia syndrome, 615877 (3), Autosomal recessive, Autosomal dominant"	Mab21l2 (MGI:1346022)			
chr4	151099572	151104651	4q31.2-q31.3	4q31.3		180478	RPS3A	Ribosomal protein S3a	RPS3A	6189	ENSG00000145425						
chr4	151103826	151103890	4q31.3	4q31.3		603568	"SNORD73A, RNU73"	"Small nucleolar RNA, C/D box 73A"	SNORD73A	8944							
chr4	151120280	151325664	4q31.3	4q31.3		608674	"SH3D19, EBP"	SH3 domain protein 19	SH3D19	152503	ENSG00000109686	fused with AML1 in t(4;21)		Sh3d19 (MGI:1350923)			
chr4	151670655	151761022	4q31.328	4q31.3		603645	"GATB, PET112"	"Glutamyl-tRNA amidotransferase, subunit B"	GATB	5188	ENSG00000059691			Gatb (MGI:2442496)			
chr4	152321257	152536872	4q31.3	4q31.3		606278	"FBXW7, AGO, CDC4"	F-box and WD40 domain protein 7	FBXW7	55294	ENSG00000109670			Fbxw7 (MGI:1354695)			
chr4	153152280	153339321	4q31.3	4q31.3		614141	"TRIM2, KIAA0517, CMT2R"	Tripartite motif-containing protein 2	TRIM2	23321	ENSG00000109654		"Charcot-Marie-Tooth disease, type 2R, 615490 (3), Autosomal recessive"	Trim2 (MGI:1933163)			
chr4	153344648	153415096	4q31.3	4q31.3		611422	MND1	"Meiotic nuclear division 1, S. cerevisiae, homolog of"	MND1	84057	ENSG00000121211			Mnd1 (MGI:1924165)			
chr4	153466345	153637607	4q31.3	4q31.3		616243	"KIAA0922, TMEM131L"	KIAA0922 gene	TMEM131L	23240	ENSG00000121210			Tmem131l (MGI:2443399)			
chr4	153684079	153710642	4q32	4q31.3		603028	"TLR2, TIL4"	Toll-like receptor-2	TLR2	7097	ENSG00000137462		"{Colorectal cancer, susceptibility to}, 114500 (3), Autosomal dominant; {Leprosy, susceptibility to}, 246300 (3), Autosomal dominant; {Mycobacterium tuberculosis, susceptibility to}, 607948 (3)"	Tlr2 (MGI:1346060)			
chr4	153780589	153789075	4q31.3	4q31.3		604157	"SFRP2, SARP1"	Secreted frizzled-related protein 2	SFRP2	6423	ENSG00000145423			Sfrp2 (MGI:108078)			
chr4	154234374	154491724	4q31.3	4q31.3		612486	"DCHS2, CDHJ, PCDHJ"	"Dachsous, Drosophila, homolog of, 2"	DCHS2	54798	ENSG00000197410						
chr4	154534996	154550432	4q31.2-q32.1	4q31.3		605961	"PLRG1, PRL1"	Pleiotropic regulator 1	PLRG1	5356	ENSG00000171566			Plrg1 (MGI:1858197)			
chr4	154562979	154572762	4q28	4q31.3		134830	FGB	"Fibrinogen, beta polypeptide"	FGB	2244	ENSG00000171564	4q31 by A; proximal to GYPB/GYPA	"Afibrinogenemia, congenital, 202400 (3), Autosomal recessive; Dysfibrinogenemia, congenital, 616004 (3); Hypofibrinogenemia, congenital, 202400 (3), Autosomal recessive"	Fgb (MGI:99501)			
chr4	154583125	154590765	4q28	4q31.3		134820	FGA	"Fibrinogen, alpha polypeptide"	FGA	2243	ENSG00000171560		"Afibrinogenemia, congenital, 202400 (3), Autosomal recessive; Amyloidosis, familial visceral, 105200 (3), Autosomal dominant; Dysfibrinogenemia, congenital, 616004 (3); Hypodysfibrinogenemia, congenital, 616004 (3)"	Fga (MGI:1316726)			
chr4	154600000	182300000	4q32-q34			612165	RP29	Retinitis pigmentosa 29	RP29	54110		maximum lod at D4S415	"Retinitis pigmentosa 29, 612165 (2), Autosomal recessive"				
chr4	154600000	163600000	4q32.1-q32.2			613603	"TRIP4q32.1q32.2, C4TRIPq32.1q32.2"	Chromosome 4q32.1-q32.2 triplication syndrome					"Chromosome 4q32.1-q32.2 triplication syndrome, 613603 (4), Autosomal dominant"				
chr4	154604133	154612807	4q28	4q32.1		134850	FGG	"Fibrinogen, gamma polypeptide"	FGG	2266	ENSG00000171557	linked to MN	"Afibrinogenemia, congenital, 202400 (3), Autosomal recessive; Dysfibrinogenemia, congenital, 616004 (3); Hypodysfibrinogenemia, 616004 (3); Hypofibrinogenemia, congenital, 202400 (3), Autosomal recessive"	Fgg (MGI:95526)			
chr4	154740840	154753118	4q31	4q32.1		604863	"LRAT, LCA14"	Lecithin retinol acyltransferase	LRAT	9227	ENSG00000121207		"Leber congenital amaurosis 14, 613341 (3), Autosomal recessive; Retinal dystrophy, early-onset severe, 613341 (3), Autosomal recessive; Retinitis pigmentosa, juvenile, 613341 (3), Autosomal recessive"	Lrat (MGI:1891259)			
chr4	155173513	155217077	4q31	4q32.1		162642	NPY2R	Neuropeptide Y receptor Y2	NPY2R	4887	ENSG00000185149			Npy2r (MGI:108418)			
chr4	155342657	155376969	4q32	4q32.1		610070	ASAP	Aster-associated protein	MAP9	79884	ENSG00000164114			Map9 (MGI:2442208)			
chr4	155666709	155737061	4q32	4q32.1		139396	"GUCY1A3, GUC1A3, GUCSA3, MYMY6"	"Guanylate cyclase 1, soluble, alpha 3"	GUCY1A1	2982	ENSG00000164116		"Moyamoya 6 with achalasia, 615750 (3), Autosomal recessive"	Gucy1a1 (MGI:1926562)			
chr4	155758972	155807641	4q32	4q32.1		139397	"GUCY1B3, GUC1B3, GUCSB3"	"Guanylate cyclase 1, soluble, beta 3"	GUCY1B1	2983	ENSG00000061918			Gucy1b1 (MGI:1860604)			
chr4	155829698	155867302	4q31.3-q32	4q32.1		616693	"ASIC5, HINAC"	Acid-sensing ion channel family member 5	ASIC5	51802	ENSG00000256394			Asic5 (MGI:1929259)			
chr4	155903692	155920405	4q31-q32	4q32.1		191070	"TDO2, TPH2, TRPO, HYPTRP"	Tryptophan oxygenase	TDO2	6999	ENSG00000151790	mutation identified in 1 HYPTRP patient	"[?Hypertryptophanemia], 600627 (3), Autosomal recessive"	Tdo2 (MGI:1928486)			
chr4	155924117	155953895	4q32.1	4q32.1		600550	CTSO	Cathepsin O	CTSO	1519	ENSG00000256043			Ctso (MGI:2139628)			
chr4	156761610	156971393	4q32	4q32.1		608452	PDGFC	Platelet-derived growth factor C	PDGFC	56034	ENSG00000145431			Pdgfc (MGI:1859631)			
chr4	157076124	157172089	4q31.3	4q32.1		138492	"GLRB, HKPX2"	"Glycine receptor, beta subunit"	GLRB	2743	ENSG00000109738		"Hyperekplexia 2, autosomal recessive, 614619 (3)"	Glrb (MGI:95751)			
chr4	157220583	157370582	4q32-q33	4q32.1		138247	"GRIA2, GLUR2"	"Glutamate receptor, ionotropic, AMPA 2"	GRIA2	2891	ENSG00000120251			Gria2 (MGI:95809)			
chr4	158521710	158653371	4q32	4q32.1		606654	"RXFP1, LGR7"	Relaxin/insulin-like family peptide receptor 1	RXFP1	59350	ENSG00000171509			Rxfp1 (MGI:2682211)			
chr4	158666674	158672254	4q32.1	4q32.1		616210	"C4orf46, RCDG1"	Chromosome 4 open reading frame 46	C4orf46	201725	ENSG00000205208			4930579G24Rik (MGI:1923189)			
chr4	158672100	158708712	4q32-qter	4q32.1		231675	"ETFDH, MADD"	Electron transfer flavoprotein:ubiquinone oxidoreductase	ETFDH	2110	ENSG00000171503		"Glutaric acidemia IIC, 231680 (3), Autosomal recessive"	Etfdh (MGI:106100)			
chr4	158709126	158723399	4q31.3	4q32.1		601753	PPID	Peptidylprolyl isomerase D (cyclophilin D)	PPID	5481	ENSG00000171497			Ppid (MGI:1914988)			
chr4	158768994	158908049	4q32.1	4q32.1		612768	"FNIP2, FNIPL, KIAA1450"	Folliculin-interacting protein 2	FNIP2	57600	ENSG00000052795			Fnip2 (MGI:2683054)			
chr4	163109132	163166920	4q32.2	4q32.2		617868	NAF1	Nuclear assembly factor 1 ribonucleoprotein	NAF1	92345	ENSG00000145414			Naf1 (MGI:2682306)			
chr4	163323964	163344831	4q31.3-q32	4q32.2		162641	NPY1R	Neuropeptide Y receptor	NPY1R	4886	ENSG00000164128			Npy1r (MGI:104963)			
chr4	163336967	163352276	4q31-q32	4q32.2		602001	NPY5R	Neuropeptide Y receptor Y5	NPY5R	4889	ENSG00000164129			Npy5r (MGI:108082)			
chr4	163524297	164384049	4q32.2-q32.3	4q32.2-q32.3		613331	1-Mar	Membrane-associated RING-CH finger protein 1	1-Mar	55016	ENSG00000145416			March1 (MGI:1920175)			
chr4	163600000	169200000	4q32.3			611109	CINN	"Cinnamon odor, pleasantness of"		100188835		max lod at AFM295YES	"[Cinnamon odor, pleasantness of], 611109 (2)"				
chr4	163600000	169200000	4q32.3			610239	HDLCQ4	High density lipoprotein cholesterol level QTL 4		100188806		between D4S1597 and D4S1539	"[High density lipoprotein cholesterol level QTL 4], 610239 (2)"				
chr4	164197006	164197710	4q32.3	4q32.3		606877	"ANP32C, PP32R1"	"Acidic leucine-rich nuclear phosphoprotein 32 family, member C"	ANP32C	23520							
chr4	164876987	164899062	4q32.3	4q32.3		615594	"ELA, LOC100506013"	Elabela	APELA	100506013	ENSG00000248329						
chr4	165207617	165323155	4q21.2	4q32.3		605774	"KLHL2, MAYVEN"	Kelch-like 2	KLHL2	11275	ENSG00000109466			Klhl2 (MGI:1924363)			
chr4	165327665	165343163	4q32-q34	4q32.3		607545	"MSMO1, SC4MOL, ERG25, MCCPD"	Methylsterol monooxygenase 1	MSMO1	6307	ENSG00000052802		"Microcephaly, congenital cataract, and psoriasiform dermatitis, 616834 (3), Autosomal recessive"	Msmo1 (MGI:1913484)			
chr4	165378941	165498546	4q32.3	4q32.3		114855	CPE	Carboxypeptidase E	CPE	1363	ENSG00000109472			Cpe (MGI:101932)			
chr4	165873123	166105177	4q32-q33	4q32.3		606742	"TLL1, TLL, ASD6"	Tolloid-like 1	TLL1	7092	ENSG00000038295		"Atrial septal defect 6, 613087 (3), Autosomal dominant"	Tll1 (MGI:106923)			
chr4	166733383	167234868	4q32.3	4q32.3		607989	SPOCK3	"SPARC/osteonectin, CWCV, and KAZAL-like domains proteoglycan 3"	SPOCK3	50859	ENSG00000196104			Spock3 (MGI:1920152)			
chr4	168092524	168187741	4q33	4q32.3		608008	ANXA10	Annexin A10	ANXA10	11199	ENSG00000109511			Anxa10 (MGI:1347090)			
chr4	168216290	168325980	4q32.3	4q32.3		613974	DDX60	DEAD box polypeptide 60	DDX60	55601	ENSG00000137628			Ddx60 (MGI:2384570)			
chr4	168356734	168480513	4q32.3	4q32.3		616725	DDX60L	DEAD box polypeptide 60-like	DDX60L	91351	ENSG00000181381						
chr4	168497038	168928456	4q32.3	4q32.3		608092	"PALLD, KIAA0992, PNCA1"	"Palladin, mouse, homolog of"	PALLD	23022	ENSG00000129116		"{Pancreatic cancer, susceptibility to, 1}, 606856 (3)"	Palld (MGI:1919583)			
chr4	169200000	190214555	4q33-qter			607258	HCA1	"Hypercalciuria, absorptive, 1"		266790			"Hypercalciuria, absorptive, 607258 (2)"				
chr4	169393269	169612628	4q33	4q33		604588	"NEK1, SRTD6, SRPS2A, ALS24"	Never in mitosis gene A-related kinase 1	NEK1	4750	ENSG00000137601	1 patient showed heterozygous NEK2 and DYNC2H1 mutations	"{Amyotrophic lateral sclerosis, susceptibility to, 24}, 617892 (3); Short-rib thoracic dysplasia 6 with or without polydactyly, 263520 (3), Autosomal recessive, Digenic recessive"	Nek1 (MGI:97303)			
chr4	169620520	169723186	4q33	4q33		600580	CLCN3	Chloride channel-3	CLCN3	1182	ENSG00000109572			Clcn3 (MGI:103555)			
chr4	169729467	169757941	4q33	4q33		616614	"HPF1, C4orf27"	Histone parylation factor 1	HPF1	54969	ENSG00000056050			Hpf1 (MGI:1919862)			
chr4	169986596	170033027	4q32.3	4q33		616523	"MFAP3L, KIAA0626"	Microfibrillar-associated protein 3-like	MFAP3L	9848	ENSG00000198948			Mfap3l (MGI:1918556)			
chr4	170060221	170091698	4q32.2	4q33		611754	"AADAT, KAT2"	Alpha-aminoadipate aminotransferase	AADAT	51166	ENSG00000109576			Aadat (MGI:1345167)			
chr4	171812655	173040407	4q34.1	4q34.1		615138	"GALNTL6, GALNACT20"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 6	GALNTL6	442117	ENSG00000174473			Galntl6 (MGI:1913581)			
chr4	173168752	173323966	4q31.1	4q34.1		605005	GALNT7	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 7	GALNT7	51809	ENSG00000109586			Galnt7 (MGI:1349449)			
chr4	173331375	173334443	4q31	4q34.1		163906	"HMGB2, HMG2"	High-mobility group box 2 (high-mobility group (nonhistone chromosomal) protein 2)	HMGB2	3148	ENSG00000164104			Hmgb2 (MGI:96157)			
chr4	173370941	173377531	4q34.1	4q34.1		603378	SAP30	"SIN3-associated polypeptide, 30kD"	SAP30	8819	ENSG00000164105			Sap30 (MGI:1929129)			
chr4	173388147	173519237	4q34.1	4q34.1		603163	SCRG1	Scraptie-responsive gene 1	SCRG1	11341	ENSG00000164106			Scrg1 (MGI:1328308)			
chr4	173526500	173530226	4q33	4q34.1		602407	"HAND2, DHAND2, DHAND"	Heart- and neural crest derivative-expressed 2	HAND2	9464	ENSG00000164107			Hand2 (MGI:103580)			
chr4	173528599	173591254	4q34.1	4q34.1		617240	"HAND2AS1, UPH, DEIN"	"HAND2 antisense RNA 1, noncoding (Upperhand)"	HAND2-AS1	79804							
chr4	173615735	173616841	4q33-q34.1	4q34.1		116960	"MORF4, SEN1, CSRB"	"Mortality factor 4 (senescence-related, cellular, 1)"	MORF4	10934							
chr4	174236657	174284250	4q34.1	4q34.1		605649	"FBXO8, FBX8, FBS"	F-box only protein 8	FBXO8	26269	ENSG00000164117			Fbxo8 (MGI:1354696)			
chr4	174423794	174423863	4q34.1	4q34.1		616274	MIR4276	Micro RNA 4276	MIR4276	100423042							
chr4	174490176	174522897	4q34-q35	4q34.1		601688	"HPGD, PGDH1, PHOAR1"	Hydroxyprostaglandin dehydrogenase 15-(NAD)	HPGD	3248	ENSG00000164120		"Cranioosteoarthropathy, 259100 (3), Autosomal recessive; Digital clubbing, isolated congenital, 119900 (3), Autosomal recessive; Hypertrophic osteoarthropathy, primary, autosomal recessive 1, 259100 (3), Autosomal recessive"	Hpgd (MGI:108085)			
chr4	174642010	174829567	4q33-q34	4q34.1		600421	GLRA3	"Glycine receptor, alpha-3 polypeptide"	GLRA3	8001	ENSG00000145451			Glra3 (MGI:95749)			
chr4	174918357	174978179	4q34	4q34.1		604778	ADAM29	A disintegrin and metalloproteinase domain 29	ADAM29	11086	ENSG00000168594			Adam29 (MGI:2676326)			
chr4	175632936	176002690	4q34	4q34.2		601275	"GPM6A, M6A"	Glycoprotein M6A	GPM6A	2823	ENSG00000150625			Gpm6a (MGI:107671)			
chr4	176065833	176182827	4q34	4q34.2		609005	WDR17	WD repeat-containing protein 17	WDR17	116966	ENSG00000150627			Wdr17 (MGI:1924662)			
chr4	176184573	176195670	4q34.1-q34.2	4q34.2		609879	"SPATA4, TSARG2"	Spermatogenesis-associated protein 4	SPATA4	132851	ENSG00000150628			Spata4 (MGI:1916531)			
chr4	176213672	176277570	4q34.2	4q34.2		615050	ASB5	Ankyrin repeat- and SOCS box-containing protein 5	ASB5	140458	ENSG00000164122			Asb5 (MGI:1923544)			
chr4	176600000	190214555	4q34.3-q35.2			600361	HMSN5	Hereditary motor and sensory neuropathy V		101059903		D4S1552 and D4S2930	"Hereditary motor and sensory neuropathy V, 600361 (2), Autosomal dominant"				
chr4	176600000	186200000	4q34.3-q35.1			613371	SCA30	Spinocerebellar ataxia 30	SCA30	100359393		between rs1397413 and rs2175476; max lod 3.0	"?Spinocerebellar ataxia 30, 613371 (2), Autosomal dominant"				
chr4	176683533	176792744	4q34.3	4q34.3		601528	"VEGFC, VRP, LMPH1D"	Vascular endothelial growth factor C	VEGFC	7424	ENSG00000150630		"Lymphedema, hereditary, ID, 615907 (3), Autosomal dominant"	Vegfc (MGI:109124)			
chr4	177430773	177442502	4q32-q33	4q34.3		613228	AGA	Aspartylglucosaminidase	AGA	175	ENSG00000038002		"Aspartylglucosaminuria, 208400 (3), Autosomal recessive"	Aga (MGI:104873)			
chr4	181447612	182803023	4q35.1	4q34.3-q35.1		610083	"TENM3, ODZ3, TNM3, KIAA1455, MCOPCB9"	Teneurin transmembrane protein 3	TENM3	55714	ENSG00000218336		"Microphthalmia, isolated, with coloboma 9, 615145 (3), Autosomal recessive"	Tenm3 (MGI:1345183)			
chr4	182300000	190214555	4q35-qter			606282	DFNA24	"Deafness, autosomal dominant 24"	DFNA24	23723			"Deafness, autosomal dominant 24, 606282 (2), Autosomal dominant"				
chr4	182300000	190214555	4q35			127600	DKBI	"Dyskeratosis, hereditary benign intraepithelial"		80870			"Dyskeratosis, hereditary benign intraepithelial, 127600 (2), Autosomal dominant"				
chr4	182300000	190214555	4q35			158900	"FSHD1, FSHD1A"	Facioscapulohumeral muscular dystrophy 1				due to D4Z4 macrosatellite repeat on 4q35	"Facioscapulohumeral muscular dystrophy 1, 158900 (4), Autosomal dominant"				
chr4	182890090	182917476	4q35	4q35.1		607638	DCTD	Deoxycytidylate deaminase	DCTD	1635	ENSG00000129187			Dctd (MGI:2444529)			
chr4	183444590	183449063	4q35.1	4q35.1		615914	"CDKN2AIP, CARF"	Cyclin-dependent kinase inhibitor 2A-interacting protein	CDKN2AIP	55602	ENSG00000168564			Cdkn2aip (MGI:1918175)			
chr4	183505049	183512427	4q35.1	4q35.1		604215	"ING2, ING1L"	Inhibitor of growth 2	ING2	3622	ENSG00000168556			Ing2 (MGI:1916510)			
chr4	183659266	183713593	4q35.1	4q35.1		614138	"TRAPPC11, C4orf41, LGMD2S"	"Trafficking protein particle complex, subunit 11"	TRAPPC11	60684	ENSG00000168538		"Muscular dystrophy, limb-girdle, type 2S, 615356 (3), Autosomal recessive"	Trappc11 (MGI:2444585)			
chr4	183796330	184023529	4q35	4q35.1		617359	"STOX2, KIAA1392"	Storkhead box 2	STOX2	56977	ENSG00000173320			Stox2 (MGI:1918319)			
chr4	184088705	184217960	4q35.1	4q35.1		616983	ENPP6	Ectonucleotide pyrophosphatase/phosphodiesterase 6	ENPP6	133121	ENSG00000164303			Enpp6 (MGI:2445171)			
chr4	184382740	184474579	4q35.1	4q35.1		147576	IRF2	Interferon regulatory factor-2	IRF2	3660	ENSG00000168310			Irf2 (MGI:96591)			
chr4	184627695	184649474	4q35	4q35.1		600636	"CASP3, CPP32"	"Caspase 3, apoptosis-related cysteine protease"	CASP3	836	ENSG00000164305			Casp3 (MGI:107739)			
chr4	184649612	184694958	4q35.1	4q35.1		615421	"CCDC111, MYP22"	Coiled-coil domain containing 111	PRIMPOL	201973	ENSG00000164306		"Myopia 22, autosomal dominant, 615420 (3), Autosomal dominant"	Primpol (MGI:3603756)			
chr4	184694064	184734131	4q35.1	4q35.1		611511	"MLF1IP, CENPU, CENP50"	MLF1-interacting protein (centromere protein U)	CENPU	79682	ENSG00000151725			Cenpu (MGI:1919126)			
chr4	184755594	184826592	4q34-q35	4q35.1		152425	"ACSL1, FACL2, FACL1, LACS, ACS1"	Acyl-CoA synthetase long-chain family member 1	ACSL1	2180	ENSG00000151726			Acsl1 (MGI:102797)			
chr4	185018840	185021264	4q35.1	4q35.1		617546	"HELT, HESL, MGN"	HELT basic helix-loop-helix transcription factor	HELT	391723	ENSG00000187821			Helt (MGI:3040955)			
chr4	185143262	185150383	4q35	4q35.1		103220	"SLC25A4, ANT1, T1, PEO3, PEO2, MTDPS12A, PEOA2"	"Solute carrier family 25 (mitochondrial carrier) member 4 (adenine nucleotide translocator-1, skeletal muscle)"	SLC25A4	291	ENSG00000151729		"Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD, 617184 (3), Autosomal dominant; Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR, 615418 (3), Autosomal recessive; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2, 609283 (3), Autosomal dominant"	Slc25a4 (MGI:1353495)			
chr4	185151722	185205442	4q35.1	4q35.1		616047	"CFAP97, HMW, KIAA1430"	Cilia- and flagella-associated protein 97	CFAP97	57587	ENSG00000164323			Cfap97 (MGI:1914006)			
chr4	185399539	185425984	4q35.1	4q35.1		611482	"UFSP2, C4orf20, BHD"	UFM1-specific protease 2	UFSP2	55325	ENSG00000109775	mutation identified in 1 BHD family	"?Hip dysplasia, Beukes type, 142669 (3), Autosomal dominant"	Ufsp2 (MGI:1913679)			
chr4	185445181	185471758	4q35.1	4q35.1		609488	KMHN1	Cancer/testis antigen KM-HN-1	CCDC110	256309	ENSG00000168491			Ccdc110 (MGI:2685018)			
chr4	185500659	185535557	4q35	4q35.1		605889	ALP	Actinin-associated LIM protein	PDLIM3	27295	ENSG00000154553						
chr4	185585443	185956715	4q35.1	4q35.1		616349	"SORBS2, ARGBP2, KIAA0777"	Sorbin and SH3 domains-containing protein 2	SORBS2	8470	ENSG00000154556			Sorbs2 (MGI:1924574)			
chr4	186069154	186085097	4q35	4q35.1		603029	"TLR3, IIAE2"	Toll-like receptor-3	TLR3	7098	ENSG00000164342		"{Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 2}, 613002 (3), Autosomal recessive, Autosomal dominant; {HIV1 infection, resistance to}, 609423 (3)"	Tlr3 (MGI:2156367)			
chr4	186191519	186213462	4q35.1	4q35.1-q35.2		608614	"CYP4V2, BCD"	"Cytochrome P450, family 4, subfamily V, polypeptide 2"	CYP4V2	285440	ENSG00000145476		"Bietti crystalline corneoretinal dystrophy, 210370 (3), Autosomal recessive"	Cyp4v3 (MGI:2142763)			
chr4	186215713	186258476	4q35	4q35.2		229000	"KLKB1, KLK3, PKKD"	Kallikrein B plasma 1 (Fletcher factor)	KLKB1	3818	ENSG00000164344	similar to F11	"Fletcher factor (prekallikrein) deficiency, 612423 (3), Autosomal recessive"	Klkb1 (MGI:102849)			
chr4	186265963	186290726	4q35	4q35.2		264900	F11	Coagulation factor XI (plasma thromboplastin antecedent)	F11	2160	ENSG00000088926	not closely linked to MNS	"Factor XI deficiency, autosomal dominant, 612416 (3); Factor XI deficiency, autosomal recessive, 612416 (3)"	F11 (MGI:99481)			
chr4	186532768	186555566	4q35.1	4q35.2		600665	MTNR1A	Melatonin receptor 1A	MTNR1A	4543	ENSG00000168412			Mtnr1a (MGI:102967)			
chr4	186587782	186726695	4q34-q35	4q35.2		600976	"FAT1, FAT"	"FAT tumor suppressor, Drosophila, homolog of, 1"	FAT1	2195	ENSG00000083857			Fat1 (MGI:109168)			
chr4	187994043	188005049	4q35.2	4q35.2		614572	"ZFP42, REX1"	Zinc finger protein 42	ZFP42	132625	ENSG00000179059			Zfp42 (MGI:99187)			
chr4	189940818	189963203	4q35	4q35.2		601278	"FRG1, FSG1"	Facioscapulohumeral muscular dystrophy region gene-1	FRG1	2483	ENSG00000109536			Frg1 (MGI:893597)			
chr4	190021168	190022664	4q35	4q35.2		615581	"DUX4L9, DUX4C"	Double homeobox 4-like 9	DUX4L9	100288711							
chr4	190024366	190027256	4q35	4q35.2		609032	FRG2	Facioscapulohumeral muscular dystrophy region gene 2	FRG2	448831	ENSG00000205097			"Frg2f8,Frg2f7,Frg2f9,Frg2f2,Frg2f1,Frg2f4,Frg2f3,Frg2f10,Frg2f6,Frg2f11,Frg2f5,Frg2f12,Frg2f13 (MGI:3643940,MGI:3782846,MGI:3782845,MGI:3779576,MGI:3647970,MGI:3779574,MGI:3647962,MGI:3648470,MGI:3644083,MGI:3648177,MGI:3035485,MGI:3643939,MGI:3805017)"			
chr4	190064501	190067863	4q35	4q35.2		614865	DBET	"D4A4 binding element transcript, noncoding"	DBET	100419743							
chr4	190067934	190069218	4q35.2	4q35.2		611442	DUX2	Double homeobox protein 2	DUX4L8	26583		?10q26.3					
chr4	190173700	190185910	4q35	4q35.2		606009	DUX4	Double homeo box protein 4	DUX4	100288687	ENSG00000260596						
chr4	0	190214555	Chr.4			151450	LAG5	Leukocyte antigen group 5		7895			"Neutropenia, neonatal alloimmune (1)"				
chr4	0	190214555	Chr.4			187320	TS13	"Temperature sensitivity complementation, ts13"		7896							
chr5	0	48800000	5p			108800	ASD1	Atrial septal defect 1	ASD1	431		max lod at D5S406	"Atrial septal defect 1, 108800 (2), Autosomal dominant"				
chr5	0	4400000	5p15.33			613059	BCC3	"Basal cell carcinoma, susceptibility to, 3"		100307120			"{Basal cell carcinoma, susceptibility to, 3}, 613059 (2)"				
chr5	0	4400000	5p15.33			613033	GLM8	Glioma susceptibility 8		100316847		associated with rs2736100	"{Glioma susceptibility 8}, 613033 (2)"				
chr5	0	4400000	5p15.33			612571	LNCR3	Lung cancer susceptibility 3		100271687		associated with rs402710 and rs2736100	"{Lung cancer susceptibility 3}, 612571 (2)"				
chr5	0	42500000	5p15.33-p13.1			608850	MCDR3	"Macular dystrophy, retinal, 3"	MCDR3	317668		maximum lod at D5S630	"Macular dystrophy, retinal, 3, 608850 (2), Autosomal dominant"				
chr5	0	48800000	5p			601888	MHS6	Malignant hyperthermia susceptibility 6	MHS6	4266			"{Malignant hyperthermia susceptibility 6}, 601888 (2)"				
chr5	0	15000000	5p15.33-p15.2			612554	MYP16	Myopia 16	MYP16	100270641		max lod at D5S2505	"Myopia 16, 612554 (2)"				
chr5	0	18400000	5p15			613637	TST2	Tuberculin skin test reactivity quantitative trait locus		100526823		max lod at 16:2.70Mb	"[Tuberculin skin test reactivity QTL], 613637 (2)"				
chr5	218222	264815	5p15	5p15.33		600857	"SDHA, SDH1, SDHF, CMD1GG, PGL5"	"Succinate dehydrogenase complex, subunit A, flavoprotein"	SDHA	6389	ENSG00000073578	copy on 3q29	"Cardiomyopathy, dilated, 1GG, 613642 (3); Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial respiratory chain complex II deficiency, 252011 (3), Autosomal recessive; Paragangliomas 5, 614165 (3), Autosomal dominant"	Sdha (MGI:1914195)			
chr5	271620	314973	5p15.33	5p15.33		601057	"PDCD6, ALG2"	Programmed cell death 6	PDCD6	10016	ENSG00000249915			Pdcd6 (MGI:109283)			
chr5	304175	438290	5p15.3	5p15.33		606517	"AHRR, KIAA1234"	Arylhydrocarbon receptor repressor	AHRR	57491	ENSG00000063438			Ahrr (MGI:1333776)			
chr5	443218	467295	5p15.33	5p15.33		608186	"EXOC3, SEC6"	Exocyst complex component 3	EXOC3	11336	ENSG00000180104			Exoc3 (MGI:2443972)			
chr5	471985	524433	5p15.3	5p15.33		182307	"SLC9A3, NHE3, DIAR8"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 3"	SLC9A3	6550	ENSG00000066230	pseudogene on chr.10	"Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive"	Slc9a3 (MGI:105064)			
chr5	612289	663499	5p15.33	5p15.33		616475	"CEP72, KIAA1519"	"Centrosomal protein, 72kD"	CEP72	55722	ENSG00000112877			Cep72 (MGI:1921720)			
chr5	659861	700726	5p15.3	5p15.33		608773	"TPPP, P25, P24"	Tubulin polymerization-promoting protein	TPPP	11076	ENSG00000171368			Tppp (MGI:1920198)			
chr5	892853	919347	5p15.33	5p15.33		604507	"TRIP13, 16E1BP, MVA3"	Thyroid hormone receptor interactor 13	TRIP13	9319	ENSG00000071539		"Mosaic variegated aneuploidy syndrome 3, 617598 (3), Autosomal recessive"	Trip13 (MGI:1916966)			
chr5	1008844	1038811	5p15.3	5p15.33		607852	NKD2	"Naked cuticle, Drosophila, homolog of, 2"	NKD2	85409	ENSG00000145506			Nkd2 (MGI:1919543)			
chr5	1050373	1155886	5p15.3	5p15.33		604879	"SLC12A7, KCC4"	"Solute carrier family 12 (potassium/chloride transporters), member 7"	SLC12A7	10723	ENSG00000113504			Slc12a7 (MGI:1342283)			
chr5	1201594	1225116	5p15.33	5p15.33		608893	"SLC6A19, HND"	"Solute carrier family 6 (neurotransmitter transporter), member 19"	SLC6A19	340024	ENSG00000174358		"Hartnup disorder, 234500 (3), Autosomal recessive; Hyperglycinuria, 138500 (3), Autosomal dominant; Iminoglycinuria, digenic, 242600 (3), Autosomal recessive, Digenic recessive"	Slc6a19 (MGI:1921588)			
chr5	1225354	1246188	5p15.33	5p15.33		610300	"SLC6A18, XTRP2"	"Solute carrier family 6 (neurotransmitter transporter), member 18"	SLC6A18	348932	ENSG00000164363			Slc6a18 (MGI:1336892)			
chr5	1253166	1295046	5p15.33	5p15.33		187270	"TERT, TCS1, EST2, DKCA2, DKCB4, PFBMFT1, CMM9"	Telomerase reverse transcriptase	TERT	7015	ENSG00000164362	deleted in cri du chat	"{Dyskeratosis congenita, autosomal dominant 2}, 613989 (3), Autosomal recessive, Autosomal dominant; {Dyskeratosis congenita, autosomal recessive 4}, 613989 (3), Autosomal recessive, Autosomal dominant; {Leukemia, acute myeloid}, 601626 (3), Autosomal dominant; {Melanoma, cutaneous malignant, 9}, 615134 (3); {Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1}, 614742 (3), Autosomal dominant"	Tert (MGI:1202709)			
chr5	1317743	1345069	5p15.33	5p15.33		612585	"CLPTM1L, CRR9"	CLPTM1-like protein	CLPTM1L	81037	ENSG00000049656			Clptm1l (MGI:2442892)			
chr5	1392789	1445427	5p15.3	5p15.33		126455	"SLC6A3, DAT1, PKDYS"	"Solute carrier family 6 (neurotransmitter transporter, dopamine), member 3"	SLC6A3	6531	ENSG00000142319		"{Nicotine dependence, protection against}, 188890 (3); Parkinsonism-dystonia, infantile, 613135 (3), Autosomal recessive"	Slc6a3 (MGI:94862)			
chr5	1461422	1523976	5p15.33	5p15.33		610472	"AYTL2, LPCAT, LPCAT1"	Acyltransferase-like 2	LPCAT1	79888	ENSG00000153395			Lpcat1 (MGI:2384812)			
chr5	1798384	1801431	5p15.3	5p15.33		611842	MRPL36	Mitochondrial ribosomal protein L36	MRPL36	64979	ENSG00000171421			Mrpl36 (MGI:2137228)			
chr5	1801381	1816050	5pter-p15.33	5p15.33		603848	NDUFS6	"NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kD"	NDUFS6	4726	ENSG00000145494		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	"Gm6415,Ndufs6 (MGI:107932,MGI:3648526)"			
chr5	1877426	1887178	5p15.3	5p15.33		606199	IRX4	Iroquois homeobox protein 4	IRX4	50805	ENSG00000113430			Irx4 (MGI:1355275)			
chr5	2707929	2751654	5p15.3	5p15.33		606198	IRX2	Iroquois homeo box protein 2	IRX2	153572	ENSG00000170561			Irx2 (MGI:1197526)			
chr5	2712590	2715236	5p15.33	5p15.33		615764	LSINCT5	Long stress-induced noncoding transcript 5	LSINCT5	101234261							
chr5	2751939	2758575	5p15.33	5p15.33		610522	CEI	Coordinated expression to IRXA2	C5orf38	153571	ENSG00000186493						
chr5	3595854	3601402	5p15.3	5p15.33		606197	IRX1	Iroquois homeo box protein 1	IRX1	79192	ENSG00000170549			Irx1 (MGI:1197515)			
chr5	5140329	5320303	5p15	5p15.32		607510	ADAMTS16	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 16"	ADAMTS16	170690	ENSG00000145536			Adamts16 (MGI:2429637)			
chr5	6300000	18400000	5p15.31-p15.1			613608	"FAME3, FCMTE3"	"Epilepsy, myoclonic, familial adult, 3"		100529229		between D5S580 and D5S2096	"Epilepsy, myoclonic, familial adult, 3, 613608 (2), Autosomal dominant"				
chr5	6371925	6378525	5p15.31	5p15.31		612382	"MED10, NUT2"	Mediator complex subunit 10	MED10	84246	ENSG00000133398			Med10 (MGI:106331)			
chr5	6437346	6496720	5p15.3	5p15.31		615832	UBE2QL1	Ubiquitin-conjugating enzyme E2Q family-like protein 1	UBE2QL1	134111	ENSG00000215218			Ube2ql1 (MGI:1924230)			
chr5	6582135	6588499	5p15.31	5p15.31		616385	"LINC01018, SRHC"	Long intergenic noncoding RNA 1018	LINC01018	255167							
chr5	6599238	6633359	5p15.31	5p15.31		610916	"NSUN2, TRM4, SAKI, MISU, MRT5"	"NOP2/SUN RNA methyltransferase family, member 2"	NSUN2	54888	ENSG00000037474		"Mental retardation, autosomal recessive 5, 611091 (3), Autosomal recessive"	Nsun2 (MGI:107252)			
chr5	6633321	6669561	5p15	5p15.31		184753	SRD5A1	"Steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)"	SRD5A1	6715	ENSG00000145545	pseudogene on X		Srd5a1 (MGI:98400)			
chr5	6713937	6757047	5p15	5p15.31		605198	"POLS, TRF4, POLK"	"Polymerase, DNA, sigma"	PAPD7	11044	ENSG00000112941			Papd7 (MGI:2682295)			
chr5	7396229	7830080	5p15.3	5p15.31		103071	ADCY2	"Adenylyl cyclase-2, brain"	ADCY2	108	ENSG00000078295			Adcy2 (MGI:99676)			
chr5	7851185	7901123	5p15.3-p15.2	5p15.31		602568	MTRR	Methionine synthase reductase	MTRR	4552	ENSG00000124275		"Homocystinuria-megaloblastic anemia, cbl E type, 236270 (3), Autosomal recessive; {Neural tube defects, folate-sensitive, susceptibility to}, 601634 (3), Autosomal recessive"	Mtrr (MGI:1891037)			
chr5	7859158	7869036	5p15.31	5p15.31		617530	FASTKD3	Fast kinase domains 3	FASTKD3	79072	ENSG00000124279			Fastkd3 (MGI:1916827)			
chr5	9035025	9546120	5p15.2	5p15.31		609297	"SEMA5A, SEMF"	Semaphorin 5a	SEMA5A	9037	ENSG00000112902			Sema5a (MGI:107556)			
chr5	9628996	9630350	5p15	5p15.31		604796	"TRB7, T2R1"	"Taste receptor, family B, member 7"	TAS2R1	50834	ENSG00000169777			Tas2r119 (MGI:2681253)			
chr5	9900000	28900000	5p15.2-p14			606770	"ADIPQTL2, CAQ5"	"Adiponectin, serum level of, QTL 2"		171511		near D5S817	"{Adiponectin, serum level of, QTL2}, 606770 (2)"				
chr5	9900000	23300000	5p15.2-p14.3			610213	ANIB4	"Aneurysm, intracranial berry, 4"	ANIB4	724058		max lod at D5S1954	"Aneurysm, intracranial berry, 4, 610213 (2)"				
chr5	10249920	10266411	5p15.2	5p15.2		610150	"CCT5, KIAA0098, CCTE"	"chaperonin containing TCP1, subunit 5 (epsilon)"	CCT5	22948	ENSG00000150753		"Neuropathy, hereditary sensory, with spastic paraplegia, 256840 (3), Autosomal recessive"	Cct5 (MGI:107185)			
chr5	10277594	10308055	5p15.2	5p15.2		613379	CMBL	Carboxymethylenebutenolidase-like protein	CMBL	134147	ENSG00000164237			Cmbl (MGI:1916824)			
chr5	10353638	10440387	5p15.2	5p15.2		613297	"MARCH6, TEB4, DOA10, KIAA0597"	Membrane-associated RING-CH finger protein 6	6-Mar	10299	ENSG00000145495			March6 (MGI:2442773)			
chr5	10441861	10482806	5p15.2	5p15.2		611756	"ROPN1L, ASP"	ROPN1-like protein	ROPN1L	83853	ENSG00000145491			Ropn1l (MGI:2182357)			
chr5	10679229	10761274	5p15.2	5p15.2		600954	DAP	Death-associated protein	DAP	1611	ENSG00000112977			Dap (MGI:1918190)			
chr5	10971839	11904066	5p15.2	5p15.2		604275	"CTNND2, NPRAP"	"Catenin, delta-2"	CTNND2	1501	ENSG00000169862			Ctnnd2 (MGI:1195966)			
chr5	12574856	12805182	5p15.2	5p15.2		617097	"LINC01194, TAG"	Long intergenic noncoding RNA 1194	LINC01194	404663							
chr5	13690327	14011828	5p15-p14	5p15.2		603335	"DNAH5, HL1, PCD, CILD3"	"Dynein, axonemal, heavy chain 5"	DNAH5	1767	ENSG00000039139		"Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 (3)"	Dnah5 (MGI:107718)			
chr5	14143349	14510203	5p15.1-p14	5p15.2		601893	"TRIO, MRD44"	Triple functional domain	TRIO	7204	ENSG00000038382		"Mental retardation, autosomal dominant 44, 617061 (3), Autosomal dominant"	Trio (MGI:1927230)			
chr5	14660793	14716551	5p15.2	5p15.2		615712	"OTULIN, FAM105B, GUM, AIPDS"	OTU deubiquitinase with linear linkage specificity	OTULIN	90268	ENSG00000154124		"Autoinflammation, panniculitis, and dermatosis syndrome, 617099 (3), Autosomal recessive"	Otulin (MGI:3577015)			
chr5	14704799	14871784	5p15.2-p14.1	5p15.2		605145	"ANKH, HANK, ANK, CMDJ, CCAL2, CPPDD"	"Ank, mouse, homolog of"	ANKH	56172	ENSG00000154122		"Chondrocalcinosis 2, 118600 (3), Autosomal dominant; Craniometaphyseal dysplasia, 123000 (3), Autosomal dominant"	Ank (MGI:3045421)			
chr5	15000000	33800000	5p15.1-p13.3			613969	MYP19	"Myopia 19, autosomal dominant"		100653370		highest lod at D5S419	"Myopia 19, 613969 (2), Autosomal dominant"				
chr5	15000000	18400000	5p15.1			608098	PVNH3	Periventricular nodular heterotopia 3		100302681			"Periventricular nodular heterotopia 3, 608098 (2)"				
chr5	15500195	15939795	5p15.1	5p15.1		605656	"FBXL7, FBL7"	F-box and leucine-rich repeat protein 7	FBXL7	23194	ENSG00000183580			Fbxl7 (MGI:3052506)			
chr5	16067305	16179787	5p15.1	5p15.1		613338	11-Mar	Membrane-associated RING-CH finger protein 11	11-Mar	441061	ENSG00000183654			March11 (MGI:3608327)			
chr5	16451518	16465784	5p15.1	5p15.1		608694	"ZNF622, ZPR9"	Zinc finger protein 622	ZNF622	90441	ENSG00000173545			Zfp622 (MGI:1289282)			
chr5	16473037	16617095	5p15.1	5p15.1		613114	"FAM134B, HSAN2B"	"Family with sequence similarity 134, member B"	RETREG1	54463	ENSG00000154153		"Neuropathy, hereditary sensory and autonomic, type IIB, 613115 (3), Autosomal recessive"	Retreg1 (MGI:1913520)			
chr5	16661906	16936275	5p15.1-p14.3	5p15.1		601481	MYO10	Myosin X	MYO10	4651	ENSG00000145555			Myo10 (MGI:107716)			
chr5	17216822	17276844	5p15.1-p14	5p15.1		605940	"BASP1, CAP23, NAP22"	"Brain-abundant signal protein, membrane-attached, 1"	BASP1	10409	ENSG00000176788			Basp1 (MGI:1917600)			
chr5	18400000	28900000	5p14			157960	MLVI2	Moloney leukemia virus integration site-2		4309							
chr5	19471295	20575885	5p15.2-p15.1	5p14.3		603019	"CDH18, CDH14"	Cadherin 18	CDH18	1016	ENSG00000145526			Cdh18 (MGI:1344366)			
chr5	21750865	22853621	5p14-p13	5p14.3		600562	"CDH12, CDHB"	Cadherin-12 (N-cadherin 2)	CDH12	1010	ENSG00000154162	pseudogene on 5q13 in SMA region		Cdh12 (MGI:109503)			
chr5	22142351	22152271	5p14	5p14.3		176793	PMCHL1	Pro-melanin-concentrating hormone-like 1	PMCHL1	5369							
chr5	23507608	23528596	5p14.2	5p14.2		609760	PRDM9	PR domain-containing protein 9	PRDM9	56979	ENSG00000164256			Prdm9 (MGI:2384854)			
chr5	24487099	24644977	5p14-p13	5p14.2-p14.1		604555	CDH10	Cadherin 10	CDH10	1008	ENSG00000040731			Cdh10 (MGI:107436)			
chr5	26880599	27038581	5p14	5p14.1		609974	CDH9	Cadherin 9	CDH9	1007	ENSG00000113100			Cdh9 (MGI:107433)			
chr5	28900000	42500000	5p13			608906	ADHD4	"Attention deficit-hyperactivity disorder, susceptibility to, 4"		450090			"{Attention deficit-hyperactivity disorder}, 143465 (2), Autosomal dominant"				
chr5	28900000	38400000	5p13.3-p13.2			607004	BDA1B	"Brachydactyly, type A1, locus B"		246260			"Brachydactyly, type A1, B, 607004 (2), Autosomal dominant"				
chr5	28900000	42500000	5p13			613174	"DUP5p13, C5DUPp13"	Chromosome 5p13 duplication syndrome					"Chromosome 5p13 duplication syndrome, 613174 (4), Isolated cases"				
chr5	28900000	67400000	5p13-q12			610262	HYT6	"Hypertension, essential, susceptibility to, 6"		100188808			"{Hypertension, essential, susceptibility to, 6}, 145500 (2), Multifactorial"				
chr5	28900000	42500000	5p13			610170	KYPSC1	Kyphoscoliosis 1		780921			"Kyphoscoliosis 1, 610170 (2)"				
chr5	31193654	31329145	5p15.1-p14	5p13.3		603007	CDH6	Cadherin 6	CDH6	1004	ENSG00000113361			Cdh6 (MGI:107435)			
chr5	31400493	31532174	5p14-p13	5p13.3		608828	"RNASEN, DROSHA, RANSE3L, RN3"	"Ribonuclease III, nuclear"	DROSHA	29102	ENSG00000113360			Drosha (MGI:1261425)			
chr5	31639387	32110931	5p13.2	5p13.3		610697	"PDZD2, PAPIN, PIN1, AIPC"	PDZ domain containing 2	PDZD2	23037	ENSG00000133401			Pdzd2 (MGI:1922394)			
chr5	32124710	32174318	5p13.3	5p13.3		612207	"GOLPH3, GPP34, MIDAS"	Golgi phosphoprotein 3	GOLPH3	64083	ENSG00000113384			Golph3 (MGI:1913879)			
chr5	32227006	32313007	5p13.3	5p13.3		606501	"MTMR12, 3PAP, KIAA1682"	Myotubularin-related protein 12	MTMR12	54545	ENSG00000150712			Mtmr12 (MGI:2443034)			
chr5	32354345	32444760	5p13.3	5p13.3		615635	ZFR	Zinc finger RNA-binding protein	ZFR	51663	ENSG00000056097			Zfr (MGI:1341890)			
chr5	32531777	32604078	5p13.3	5p13.3		600503	"SUB1, PC4, p15"	"Sub1, S. cerevisiae, homolog of"	SUB1	10923	ENSG00000113387			Sub1 (MGI:104811)			
chr5	32689075	32791723	5p14-p12	5p13.3		108962	"NPR3, ANPRC"	Natriuretic peptide receptor C	NPR3	4883	ENSG00000113389		"?Hypertension, salt-resistant (1)"	Npr3 (MGI:97373)			
chr5	33440695	33468090	5p13-cen	5p13.3		187790	TARS	Threonyl-tRNA synthetase	TARS	6897	ENSG00000113407	linked to LARS		Tars (MGI:106314)			
chr5	33523534	33892191	5q35	5p13.3-p13.2		606184	ADAMTS12	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 12"	ADAMTS12	81792	ENSG00000151388			Adamts12 (MGI:2146046)			
chr5	33800000	38400000	5p13.2			612595	MS3	"Multiple sclerosis, susceptibility to, 3"		100271695		associated with rs6897932	"{Multiple sclerosis, susceptibility to, 3}, 612595 (2)"				
chr5	33936385	33938917	5p15.1-p14	5p13.2		609445	"RXFP3, RLN3R1, SALPR, GPCR135"	Relaxin/insulin-like family peptide receptor 3	RXFP3	51289	ENSG00000182631			Rxfp3 (MGI:2441827)			
chr5	33944615	33984674	5p13.3	5p13.2		606202	"SLC45A2, MATP, AIM1, SHEP5, OCA4"	"Solute carrier family 45, member 2"	SLC45A2	51151	ENSG00000164175		"Albinism, oculocutaneous, type IV, 606574 (3); [Skin/hair/eye pigmentation 5, black/nonblack hair], 227240 (3), Autosomal recessive; [Skin/hair/eye pigmentation 5, dark/fair skin], 227240 (3), Autosomal recessive; [Skin/hair/eye pigmentation 5, dark/light eyes], 227240 (3), Autosomal recessive"	Slc45a2 (MGI:2153040)			
chr5	33986985	34008114	5p13.2-q11.1	5p13.2		604489	"AMACR, CBAS4, AMACRD"	Alpha-methylacyl-CoA racemase	AMACR	23600	ENSG00000242110		"Alpha-methylacyl-CoA racemase deficiency, 614307 (3), Autosomal recessive; Bile acid synthesis defect, congenital, 4, 214950 (3), Autosomal recessive"	Amacr (MGI:1098273)			
chr5	34017857	34244723	5p13	5p13.2		612045	"C1ATNF3, CTRP3, CORS26"	C1q- and tumor necrosis factor-related protein 3	C1QTNF3	114899	ENSG00000082196			C1qtnf3 (MGI:1932136)			
chr5	34656302	34832611	5p13.3-p13.2	5p13.2		606586	"RAI14, KIAA1334"	Retinoic acid-induced 14	RAI14	26064	ENSG00000039560			Rai14 (MGI:1922896)			
chr5	34839163	34900510	5p13.2	5p13.2		616344	TTC23L	Tetratricopeptide repeat domain-containing protein 23-like	TTC23L	153657	ENSG00000205838			Ttc23l (MGI:1923027)			
chr5	34905259	34915674	5p13.3-p13.2	5p13.2		603153	RAD1	"RAD1, S. pombe, homolog of"	RAD1	5810	ENSG00000113456			Rad1 (MGI:1316678)			
chr5	34929539	34958963	5p13.2	5p13.2		617048	"DNAJC21, DNAJA5, BMFS3"	"DNAJ/HSP40 homolog, subfamily C, member 21"	DNAJC21	134218	ENSG00000168724		"Bone marrow failure syndrome 3, 617052 (3), Autosomal recessive"	Dnajc21 (MGI:1925371)			
chr5	34998098	35048187	5p13	5p13.2		612471	"AGXT2, AGT2, BAIBA"	Alanine-glyoxylate aminotransferase 2	AGXT2	64902	ENSG00000113492		"[Beta-aminoisobutyric acid, urinary excretion of], 210100 (3), Autosomal recessive"	Agxt2 (MGI:2146052)			
chr5	35048755	35230723	5p13.2	5p13.2		176761	"PRLR, MFAB, HPRL"	Prolactin receptor	PRLR	5618	ENSG00000113494	mutation identified in 1 family with HPRL	"?Hyperprolactinemia, 615555 (3), Autosomal dominant; Multiple fibroadenomas of the breast, 615554 (3), Autosomal dominant"	Prlr (MGI:97763)			
chr5	35617366	35814610	5p13.2	5p13.2		610172	"SPEF2, KPL2, KIAA1770"	Sperm flagellar 2	SPEF2	79925	ENSG00000152582			Spef2 (MGI:2443727)			
chr5	35856848	35879602	5p13	5p13.2		146661	"IL7R, IL7RA, CD127"	Interleukin-7 receptor	IL7R	3575	ENSG00000168685		"Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type, 608971 (3), Autosomal recessive"	Il7r (MGI:96562)			
chr5	35953088	36001054	5p13.2	5p13.2		616383	UGT3A1	"Uridine diphosphate glucuronosyltransferase 3 family, member A1"	UGT3A1	133688	ENSG00000145626			"Ugt3a1,Ugt3a2 (MGI:2145969,MGI:2146055)"			
chr5	36035016	36071357	5p13.2	5p13.2		616384	UGT3A2	"Uridine diphosphate glucuronosyltransferase 3 family, member A2"	UGT3A2	167127	ENSG00000168671						
chr5	36152042	36184040	5p13	5p13.2		601436	SKP2	S-phase kinase-associated protein 2 (p45)	SKP2	6502	ENSG00000145604			Skp2 (MGI:1351663)			
chr5	36192588	36242278	5p13.2	5p13.2		615787	"NADK2, C5orf33, DECRD"	"NAD kinase 2, mitochondrial"	NADK2	133686	ENSG00000152620	mutation identified in 1 DECRD family	"?2,4-dienoyl-CoA reductase deficiency, 616034 (3), Autosomal recessive"	Nadk2 (MGI:1915896)			
chr5	36246918	36301908	6p13.2	5p13.2		616391	RANBP3L	RAN-binding protein 3-like	RANBP3L	202151	ENSG00000164188			Ranbp3l (MGI:2444654)			
chr5	36606354	36688333	5p13	5p13.2		600111	"SLC1A3, EAAT1, EA6"	"Solute carrier family 1 (glial high affinity glutamate transporter), member 3"	SLC1A3	6507	ENSG00000079215		"Episodic ataxia, type 6, 612656 (3), Autosomal dominant"	Slc1a3 (MGI:99917)			
chr5	36876758	37065818	5p13.1	5p13.2		608667	"NIPBL, CDLS1"	Nipped-B-like (delangin)	NIPBL	25836	ENSG00000164190		"Cornelia de Lange syndrome 1, 122470 (3), Autosomal dominant"	Nipbl (MGI:1913976)			
chr5	37063927	37249498	5p13.2	5p13.2		614571	"C5orf42, JBTS17, OFD6"	Chromosome 5 open reading frame 42	CPLANE1	65250	ENSG00000197603		"Joubert syndrome 17, 614615 (3), Autosomal recessive; Orofaciodigital syndrome VI, 277170 (3), Autosomal recessive"	2410089E03Rik (MGI:1920942)			
chr5	37291632	37371125	5p13	5p13.2		606694	"NUP155, KIAA0791, ATFB15"	"Nucleoporin, 155kD"	NUP155	9631	ENSG00000113569	mutation identified in 1 ATFB15 family	"?Atrial fibrillation 15, 615770 (3), Autosomal recessive"	Nup155 (MGI:2181182)			
chr5	37379259	37752671	5p13.2	5p13.2		617233	WDR70	WD repeat-containing protein 70	WDR70	55100	ENSG00000082068			Wdr70 (MGI:1921020)			
chr5	37812676	37840043	5p13.1-p12	5p13.2		600837	"GDNF, HSCR3"	Glial cell line derived neurotrophic factor	GDNF	2668	ENSG00000168621		"Central hypoventilation syndrome, 209880 (3), Autosomal dominant; {Hirschsprung disease, susceptibility to, 3}, 613711 (3), Autosomal dominant; {Pheochromocytoma, modifier of}, 171300 (3), Autosomal dominant"	Gdnf (MGI:107430)			
chr5	38258408	38465479	5p13.2-p13.1	5p13.2-p13.1		617683	"EGFLAM, PIKA, AGRINL"	"EGF-like, fibronectin type III, and laminin G domains-containing protein"	EGFLAM	133584	ENSG00000164318			Egflam (MGI:2146149)			
chr5	38400000	42500000	5p13.1			612262	IBD18	Inflammatory bowel disease 18		100190931		associated with rs1373692	"{Inflammatory bowel disease 18}, 612262 (2)"				
chr5	38474962	38606289	5p13.1	5p13.1		151443	"LIFR, STWS, SWS, SJS2"	Leukemia inhibitory factor receptor	LIFR	3977	ENSG00000113594		"Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, 601559 (3), Autosomal recessive"	Lifr (MGI:96788)			
chr5	38845857	38945578	5p13.1	5p13.1		601743	"OSMR, OSMRB, PLCA1"	Oncostatin M receptor	OSMR	9180	ENSG00000145623		"Amyloidosis, primary localized cutaneous, 1, 105250 (3), Autosomal dominant"	Osmr (MGI:1330819)			
chr5	39105251	39274499	5p13.1	5p13.1		602731	"FYB, SLAP130, ADAP, THC3"	FYN-binding protein	FYB1	2533	ENSG00000082074		"Thrombocytopenia 3, 273900 (3), Autosomal recessive"	Fyb (MGI:1346327)			
chr5	39284143	39364559	5p13	5p13.1		120940	"C9, C9D, ARMD15"	Complement component-9	C9	735	ENSG00000113600		"C9 deficiency, 613825 (3); {Macular degeneration, age-related, 15, susceptibility to}, 615591 (3)"	C9 (MGI:1098282)			
chr5	39371673	39425232	5p13	5p13.1		601236	"DAB2, DOC2"	"Disabled, Drosophila, homolog of, 2 (differentially expressed in ovarian cancer-2)"	DAB2	1601	ENSG00000153071			Dab2 (MGI:109175)			
chr5	40679929	40740935	5p13.1	5p13.1		601586	PTGER4	"Prostaglandin E receptor 4, EP4 subtype"	PTGER4	5734	ENSG00000171522			Ptger4 (MGI:104311)			
chr5	40759378	40798194	5p12	5p13.1		602739	PRKAA1	"Protein kinase, AMP-activated, catalytic, alpha-1"	PRKAA1	5562	ENSG00000132356			Prkaa1 (MGI:2145955)			
chr5	40831327	40835284	5p	5p13.1		604181	RPL37	Ribosomal protein L37	RPL37	6167	ENSG00000145592			Rpl37 (MGI:1914531)			
chr5	40841196	40855353	5p13.1-p12	5p13.1		609986	"CARD6, CINCIN1"	Caspase recruitment domain-containing protein 6	CARD6	84674	ENSG00000132357			Card6 (MGI:3032959)			
chr5	40909251	40984639	5p13	5p13.1		217070	C7	Complement component-7	C7	730	ENSG00000112936		"C7 deficiency, 610102 (3)"	C7 (MGI:88235)			
chr5	41142145	41261485	5p13	5p13.1		217050	C6	Complement component-6	C6	729	ENSG00000039537		"C6 deficiency, 612446 (3); Combined C6/C7 deficiency (3)"	C6 (MGI:88233)			
chr5	41306945	41510627	5p13.1	5p13.1		617016	PLCXD3	"Phospholipase C, phosphatidylinositol-specific, X domain-containing protein 3"	PLCXD3	345557	ENSG00000182836			Plcxd3 (MGI:2442605)			
chr5	41730064	41870688	5p13	5p13.1		601424	"OXCT1, OXCT, SCOT"	3-oxoacid CoA transferase 1	OXCT1	5019	ENSG00000083720		"Succinyl CoA:3-oxoacid CoA transferase deficiency, 245050 (3)"	Oxct1 (MGI:1914291)			
chr5	41918060	42040229	5p12	5p13.1		609090	"FBXO4, FBX4"	F-box only protein 4	FBXO4	26272	ENSG00000151876			Fbxo4 (MGI:2146220)			
chr5	42423774	42721877	5p13-p12	5p13-p12		600946	"GHR, GHIP"	Growth hormone receptor	GHR	2690	ENSG00000112964		"Growth hormone insensitivity, partial, 604271 (3); {Hypercholesterolemia, familial, modifier of}, 143890 (3), Autosomal dominant; Increased responsiveness to growth hormone (3); Laron dwarfism, 262500 (3), Autosomal recessive"	Ghr (MGI:95708)			
chr5	42799879	42812075	5p11	5p12		601484	"SELENOP, SEPP1"	Selenoprotein P	SELENOP	6414	ENSG00000250722			Selenop (MGI:894288)			
chr5	43039079	43040344	5p12	5p12		611296	"ANXA2R, C5orf39, AX2R, AXIIR"	Annexin A2 receptor	ANXA2R	389289	ENSG00000177721						
chr5	43120842	43176323	5p12-p11	5p12		604073	ZNF131	Zinc finger protein -31	ZNF131	7690	ENSG00000172262			Zfp131 (MGI:1919715)			
chr5	43287469	43313511	5p14-p13	5p12		142940	HMGCS1	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1	HMGCS1	3157	ENSG00000112972	"like HMGCR, regulated transcriptionally by steroid"		Hmgcs1 (MGI:107592)			
chr5	43356971	43412390	5p12	5p12		605240	CCL28	"Chemokine, C-C motif, ligand 28"	CCL28	56477	ENSG00000151882			Ccl28 (MGI:1861731)			
chr5	43526266	43557418	5p12	5p12		605184	PAIP1	Polyadenylate-binding protein-interacting protein 1	PAIP1	10605	ENSG00000172239			Paip1 (MGI:2384993)			
chr5	43601091	43705565	5p12	5p12		607878	"NNT, GCCD4"	Nicotinamide nucleotide transhydrogenase	NNT	23530	ENSG00000112992		"Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency, 614736 (3), Autosomal recessive"				
chr5	44301654	44389705	5p13-p12	5p12		602115	FGF10	Fibroblast growth factor-10	FGF10	2255	ENSG00000070193		"Aplasia of lacrimal and salivary glands, 180920 (3), Autosomal dominant; LADD syndrome, 149730 (3), Autosomal dominant"	Fgf10 (MGI:1099809)			
chr5	44808924	44815513	5p12-q11	5p12		611991	MRPS30	Mitochondrial ribosomal protein S30	MRPS30	10884	ENSG00000112996			Mrps30 (MGI:1926237)			
chr5	45254949	45696117	5p12	5p12		602780	"HCN1, BCNG1, EIEE24"	Hyperpolarization-activated cyclic nucleotide-gated potassium channel 1	HCN1	348980	ENSG00000164588		"Epileptic encephalopathy, early infantile, 24, 615871 (3), Autosomal dominant"	Hcn1 (MGI:1096392)			
chr5	48800000	181538259	5q			609657	BSZQTL2	Bone size quantitative trait locus 2		100188794			"{Bone size QTL}, 609657 (2)"				
chr5	50396191	50443298	5q11.1	5q11.1		615669	"EMB, GP70"	Embigin	EMB	133418	ENSG00000170571			Emb (MGI:95321)			
chr5	51383123	51394729	5q	5q11.1		600366	ISL1	"ISL1 transcription factor, LIM/homeodomain (islet-1)"	ISL1	3670	ENSG00000016082	between D5S395 and D5S407; proximal 5q		Isl1 (MGI:101791)			
chr5	52787939	52802616	5q11.2	5q11.2		605757	PELO	"Pelota, Drosophila, homolog of"	PELO	53918	ENSG00000152684			Pelo (MGI:2145154)			
chr5	52788301	52953654	5q11.2	5q11.2		192968	"ITGA1, VLA1"	"Integrin, alpha-1"	ITGA1	3672	ENSG00000213949			Itga1 (MGI:96599)			
chr5	52989325	53094778	5q23-q31	5q11.2		192974	"ITGA2, CD49B, BR, BDPLT9"	"Integrin, alpha-2 (CD49B; alpha-2 subunit of VLA-2 receptor; platelet antigen Br)"	ITGA2	3673	ENSG00000164171		"?Glycoprotein Ia deficiency, 614200 (1), Autosomal dominant"	Itga2 (MGI:96600)			
chr5	53095678	53109771	5q11	5q11.2		603708	"MOCS2, MPTS, MOCODB"	Molybdenum cofactor synthesis-2	MOCS2	4338	ENSG00000164172		"Molybdenum cofactor deficiency B, 252160 (3), Autosomal recessive"	Mocs2 (MGI:1336894)			
chr5	53480337	53487133	5q11.2	5q11.2		136470	"FST, FS"	Follistatin	FST	10468	ENSG00000134363			Fst (MGI:95586)			
chr5	53560609	53683340	5q11.1	5q11.2		602694	"NDUFS4, AQDQ"	"NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kD (NADH-coenzyme Q reductase)"	NDUFS4	4724	ENSG00000164258		"Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufs4 (MGI:1343135)			
chr5	54455600	54456383	5q11.2	5q11.2		604624	"HSPB3, HSPL27, HMN2C, DHMN2C"	Heat-shock 27kD protein 3	HSPB3	8988	ENSG00000169271	mutation identified in 1 HMN2C family	"?Neuronopathy, distal hereditary motor, type IIC, 613376 (3), Autosomal dominant"	Hspb3 (MGI:1928479)			
chr5	54977866	54985585	5q11.2	5q11.2		601521	ESM1	Endothelial cell-specific molecule 1	ESM1	11082	ENSG00000164283			Esm1 (MGI:1918940)			
chr5	55024278	55034131	5q11.2	5q11.2		600784	"GZMK, TRYP2"	Granzyme K	GZMK	3003	ENSG00000113088			Gzmk (MGI:1298232)			
chr5	55102645	55110251	5q11-q12	5q11.2		140050	"GZMA, CTLA3, HFSP"	Granzyme A (Cytotoxic T-lymphocyte-associated serine esterase-3; Hanukah factor serine protease)	GZMA	3001	ENSG00000145649			Gzma (MGI:109266)			
chr5	55160117	55167300	5q11.2	5q11.2		617172	GPX8	Glutathione peroxidase 8	GPX8	493869	ENSG00000164294			Gpx8 (MGI:1916840)			
chr5	55170531	55170621	5q11.2	5q11.2		613131	"MIR449A, MIRN449A"	Micro RNA 449A	MIR449A	554213							
chr5	55170645	55170741	5q11.2	5q11.2		613132	"MIR449B, MIRN449B"	Micro RNA 449B	MIR449B	693123							
chr5	55218790	55227314	5q11.2	5q11.2		614086	IDAS	IDAS	MCIDAS	345643	ENSG00000234602			Mcidas (MGI:3648807)			
chr5	55231151	55233716	5q11.2	5q11.2		607752	"CCNO, UNG2, CILD29"	Cyclin O	CCNO	10309	ENSG00000152669		"Ciliary dyskinesia, primary, 29, 615872 (3), Autosomal recessive"	Ccno (MGI:2145534)			
chr5	55256054	55307721	5q11.2	5q11.2		612720	DHX29	DEAH (Asp-Glu-Ala-His) box polypeptide 29	DHX29	54505	ENSG00000067248			Dhx29 (MGI:2145374)			
chr5	55424841	55535077	5q11.2	5q11.2		607124	"PLPP1, PPAP2A"	Phopshplipid phosphatase 1	PLPP1	8611	ENSG00000067113						
chr5	55625844	55712342	5q11.2	5q11.2		616203	"SLC38A9, URLC11"	"Solute carrier family 38, member 9"	SLC38A9	153129	ENSG00000177058			Slc38a9 (MGI:1918839)			
chr5	55737993	55817145	5q11.2-q12	5q11.2		605281	"DDX4, VASA"	"DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 4 (vasa, Drosophila, homolog of)"	DDX4	54514	ENSG00000152670			Ddx4 (MGI:102670)			
chr5	55840333	55922853	5q11.2	5q11.2		609510	"IL31RA, GLMR, GPL, PLCA2"	Interleukin 31 receptor A	IL31RA	133396	ENSG00000164509	mutation identified in 1 PLCA2 patient	"?Amyloidosis, primary localized cutaneous, 2, 613955 (3), Autosomal dominant"	Il31ra (MGI:2180511)			
chr5	55935094	55994992	5q11	5q11.2		600694	IL6ST	"Interleukin-6 signal transducer (gp130, oncostatin M receptor)"	IL6ST	3572	ENSG00000134352			Il6st (MGI:96560)			
chr5	56099679	56233358	5q11	5q11.2		615189	ANKRD55	Ankyrin repeat domain-containing protein 55	ANKRD55	79722	ENSG00000164512			Ankrd55 (MGI:1924568)			
chr5	56815072	56896151	5q11.2	5q11.2		600982	"MAP3K1, MEKK1, MEKK, SRXY6"	Mitogen-activated protein kinase kinase kinase 1	MAP3K1	4214	ENSG00000095015		"46XY sex reversal 6, 613762 (3), Autosomal dominant"	Map3k1 (MGI:1346872)			
chr5	57173841	57264678	5q11.2	5q11.2		608412	"GPBP1, GPBP"	GC-rich promoter-binding protein 1	GPBP1	65056	ENSG00000062194			Gpbp1 (MGI:1920524)			
chr5	57480015	57482808	5q11.2	5q11.2		614835	ACTBL2	"Actin, beta-like, 2"	ACTBL2	345651	ENSG00000169067			Actbl2 (MGI:2444552)			
chr5	58453981	58460138	5q12-q13	5q11.2		607023	"PLK2, SNK"	Polo-like kinase 2	PLK2	10769	ENSG00000145632			Plk2 (MGI:1099790)			
chr5	58582187	58859393	5q13	5q11.2		612829	RAB3C	Ras-associated protein RAB3C	RAB3C	115827	ENSG00000152932			Rab3c (MGI:1914545)			
chr5	58969037	60524328	5q12	5q11.2-q12.1		600129	"PDE4D, DPDE3, STRK1, ACRDYS2"	"Phosphodiesterase-4D, cAMP-specific (dunce, Drosophila, homolog of, phosphodiesterase-E3)"	PDE4D	5144	ENSG00000113448		"Acrodysostosis 2, with or without hormone resistance, 614613 (3), Autosomal dominant; {Stroke, susceptibility to, 1}, 606799 (3)"				
chr5	59600000	67400000	5q12			615668	"DEL5q12, C5DELq12"	Chromosome 5q12 deletion syndrome					"Chromosome 5q12 deletion syndrome, 615668 (4), Autosomal dominant"				
chr5	59600000	93000000	5q12-q14			611364	EJM4	"Myoclonic epilepsy, juvenile, 4"		100126594		max lod at D5S459	"Myoclonic epilepsy, juvenile, 4, 611364 (2), Autosomal dominant"				
chr5	60487712	60547656	5q12	5q12.1		604991	PART1	Prostate androgen-regulated transcript 1	PART1	25859							
chr5	60596911	60700165	5q12.1	5q12.1		616073	DEPDC1B	DEP domain-containing protein 1B	DEPDC1B	55789	ENSG00000035499			Depdc1b (MGI:2145425)			
chr5	60751788	60844291	5q12.1	5q12.1		614451	ELOVL7	Elongation of very long chain fatty acids-like 6	ELOVL7	79993	ENSG00000164181			Elovl7 (MGI:1921809)			
chr5	60873831	60945077	5q12	5q12.1		609412	"ERCC8, CKN1, CSA, UVSS2"	"Excision repair cross-complementing rodent repair deficiency, complementation group 8"	ERCC8	1161	ENSG00000049167		"Cockayne syndrome, type A, 216400 (3), Autosomal recessive; UV-sensitive syndrome 2, 614621 (3), Autosomal recessive"	Ercc8 (MGI:1919241)			
chr5	60945128	61153036	5q12.1	5q12.1		609653	"NDUFAF2, NDUFA12L, MMTN, B17.2L"	"NADH dehydrogenase 1 alpha subcomplex, assembly factor 2"	NDUFAF2	91942	ENSG00000164182	pseudogene on chr.2	"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufaf2 (MGI:1922847)			
chr5	61332272	61546171	5q12.1	5q12.1		615951	"ZSWIM6, KIAA1577, AFND, NEDMAGA"	Zinc finger SWIM domain-containing protein 6	ZSWIM6	57688	ENSG00000130449		"Acromelic frontonasal dysostosis, 603671 (3), Autosomal dominant; Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, 617865 (3), Autosomal dominant"	Zswim6 (MGI:1914513)			
chr5	62306161	62387183	5q12.1	5q12.1		602591	"KIF2A, CDCBM3"	"Kinesin, heavy chain, 2"	KIF2A	3796	ENSG00000068796		"Cortical dysplasia, complex, with other brain malformations 3, 615411 (3), Autosomal dominant"	Kif2a (MGI:108390)			
chr5	62387952	62403959	5q12.1	5q12.1		612499	"DIMT1L, DIM1, HUSSY5"	Dimethyladenosine transferase 1-like	DIMT1	27292	ENSG00000086189	previously assigned to 8p12		Dimt1 (MGI:1913504)			
chr5	62412745	62628588	5q12.1	5q12.1		610889	"IPO11, RANBP11, SLRN"	Importin 11	IPO11	51194	ENSG00000086200			Ipo11 (MGI:2442377)			
chr5	63960047	63962291	5q11.2-q13	5q12.3		109760	"HTR1A, ADRB2RL1, PFMCD"	5-hydroxytryptamine (serotonin) receptor-1A	HTR1A	3350	ENSG00000178394		"Periodic fever, menstrual cycle dependent, 614674 (3), Autosomal dominant"	Htr1a (MGI:96273)			
chr5	64165310	64372878	5q12.3	5q12.3		616015	"RNF180, RINES"	RING finger protein 180	RNF180	285671	ENSG00000164197			Rnf180 (MGI:1919066)			
chr5	64505946	64612329	5q12.3	5q12.3		610890	"RGS7BP, R7BP"	Regulator of G protein signaling 7-binding protein	RGS7BP	401190	ENSG00000186479			Rgs7bp (MGI:106334)			
chr5	64768917	65018762	5q12.3	5q12.3		617170	"CWC27, SDCCAG10, RPSKA"	"CWC27 spliceosome-associated protein, X. cerevisiae, homolog of"	CWC27	10283	ENSG00000153015		"Retinitis pigmentosa with or without skeletal anomalies, 250410 (3), Autosomal recessive"	Cwc27 (MGI:1914535)			
chr5	65148735	65482662	5q12	5q12.3		605008	ADAMTS6	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 6"	ADAMTS6	11174	ENSG00000049192			Adamts6 (MGI:1347348)			
chr5	65488918	65563193	5p15.2-q12.3	5q12.3		611502	"CEMPK, SOLT"	Centromeric protein K	CENPK	64105	ENSG00000123219			Cenpk (MGI:1926210)			
chr5	65589679	65624359	5q12.3	5q12.3		601747	"TRIM23, ARD1"	Tripartite motif-containing protein 23	TRIM23	373	ENSG00000113595			Trim23 (MGI:1933161)			
chr5	65722195	65829282	5q12.3	5q12.3		611530	"NLN, KIAA1226, AGTBP"	Neurolysin	NLN	57486	ENSG00000123213			Nln (MGI:1923055)			
chr5	65926553	66081022	5q12	5q12.3		606944	"ERBB2IP, ERBIN"	ERBB2 interacting protein	ERBIN	55914	ENSG00000112851			Erbin (MGI:1890169)			
chr5	66144217	66183615	5q11.2-q12.1	5q12.3		609268	"SREK1, SFRS12, SRRp508"	Splicing regulatory glutamine/lysine-rich protein 1	SREK1	140890	ENSG00000153914			Srek1 (MGI:2145245)			
chr5	67182274	67196788	5q12	5q12.3		602226	"CD180, LY64, RP105"	CD180 antigen	CD180	4064	ENSG00000134061			Cd180 (MGI:1194924)			
chr5	67400000	93000000	5q13-q14			607087	"AAT2, FAA2"	"Aortic aneurysm, familial thoracic 2"		252843			"Aortic aneurysm, familial thoracic 2, 607087 (2)"				
chr5	67400000	115900000	5q13-q22			605544	"GINGF2, GGF2, HGF2"	"Fibromatosis, gingival, 2"	GINGF2	64644		formerly GINGF2 used for a locus on 2p16-p13	"Fibromatosis, gingival, 2, 605544 (2)"				
chr5	67400000	77600000	5q13			612306	TSHQTL1	Thyroid-stimulating hormone level QTL 1		100190789		associated with rs4704397	"[Thyroid-stimulating hormone level QTL 1], 612306 (2)"				
chr5	68215736	68301820	5q13	5q13.1		171833	"PIK3R1, GRB1, AGM7, SHORT, IMD36"	"Phosphatidylinositol 3-kinase, regulatory, 1"	PIK3R1	5295	ENSG00000145675	mutation identified in 1 AGM7 family	"?Agammaglobulinemia 7, autosomal recessive, 615214 (3), Autosomal recessive; Immunodeficiency 36, 616005 (3), Autosomal dominant; SHORT syndrome, 269880 (3), Autosomal dominant"	Pik3r1 (MGI:97583)			
chr5	69093948	69131071	5q11.2	5q13.1-q13.2		607819	"SLC30A5, ZNT5, ZTL1"	"Solute carrier family 30 (zinc transporter), member 5"	SLC30A5	64924	ENSG00000145740			Slc30a5 (MGI:1916298)			
chr5	69167009	69178244	5q12	5q13.2		123836	CCNB1	Cyclin B1	CCNB1	891	ENSG00000134057			"Ccnb1,Ccnb1-ps (MGI:88302,MGI:3648694)"			
chr5	69189547	69210356	5q13.2	5q13.2		605607	CENPH	Centromeric protein H	CENPH	64946	ENSG00000153044			Cenph (MGI:1349448)			
chr5	69217745	69230157	5q12.1	5q13.2		611996	MRPS36	Mitochondrial ribosomal protein S36	MRPS36	92259	ENSG00000134056	6 pseudogenes		Mrps36 (MGI:1913378)			
chr5	69234794	69277429	5q13.2	5q13.2		601955	"CDK7, STK1, CAK1"	Cyclin-dependent kinase 7 (homolog of Xenopus MO15 cdk-activating kinase)	CDK7	1022	ENSG00000134058	previously mapped to 2p15-cen		Cdk7 (MGI:102956)			
chr5	69273086	69333069	5q13.2	5q13.2		613781	"CCDC125, KENAE"	Coiled-coil domain-containing protein 125	CCDC125	202243	ENSG00000183323			Ccdc125 (MGI:1923291)			
chr5	69364742	69370012	5q11.2-q13.1	5q13.2		600822	"TAF9, TAF2G, TAFII32"	"TAF9 RNA polymerase II, TATA box-binding protein-associated factor, 32kD"	TAF9	6880	ENSG00000273841			Taf9 (MGI:1888697)			
chr5	69369296	69414800	5q13	5q13.2		603139	RAD17	"RAD17, S. pombe, homolog of"	RAD17	5884	ENSG00000152942			Rad17 (MGI:1333807)			
chr5	69415111	69444021	5q13.1	5q13.2		610572	"MARVELD2, MARVD2, TRIC, DFNB49"	Marvel domain-containing protein 2 (tricellulin)	MARVELD2	153562	ENSG00000152939		"Deafness, autosomal recessive 49, 610153 (3), Autosomal recessive"	Marveld2 (MGI:2446166)			
chr5	69492291	69558103	5q13.1	5q13.2		602876	"OCLN, BLCPMG, PTORCH1"	Occludin	OCLN	100506658	ENSG00000197822		"Pseudo-TORCH syndrome 1, 251290 (3), Autosomal recessive"	Ocln (MGI:106183)			
chr5	70049522	70077594	5q12.2-q13.3	5q13.2		601627	SMN2	"Survival of motor neuron 2, centromeric"	SMN2	6607	ENSG00000205571		"{Spinal muscular atrophy, type III, modifier of}, 253400 (3), Autosomal recessive"	Smn1 (MGI:109257)			
chr5	70900662	70918529	5q12.2-q13.3	5q13.2		603011	"SERF1A, H4F5, SMAM1"	Small EDRK-rich factor 1A	SERF1A	8293	ENSG00000205572			Serf1 (MGI:1337114)			
chr5	70924940	70953014	5q12.2-q13.3	5q13.2		600354	"SMN1, SMA1, SMA2, SMA3, SMA4"	"Survival of motor neuron 1, telomeric"	SMN1	6606	ENSG00000205571		"Spinal muscular atrophy-1, 253300 (3), Autosomal recessive; Spinal muscular atrophy-2, 253550 (3), Autosomal recessive; Spinal muscular atrophy-3, 253400 (3), Autosomal recessive; Spinal muscular atrophy-4, 271150 (3), Autosomal recessive"	Smn1 (MGI:109257)			
chr5	70968482	71025113	5q12.2-q13.3	5q13.2		600355	"BIRC1, NAIP"	Baculoviral IAP repeat-containing 1 (neuronal apoptosis inhibitory protein)	NAIP	4671	ENSG00000249437	?involved in SMA		Naip2 (MGI:1298226)			
chr5	71035123	71109112	5q12.2-q13.3	5q13.2		601748	GTF2H2	"General transcription factor IIH, polypeptide 2 (44kD subunit)"	GTF2H2	2966	ENSG00000145736	2 copies		Gtf2h2 (MGI:1345669)			
chr5	71375784	71385992	5q12-q13	5q13.2		176794	PMCHL2	Pro-melanin-concentrating hormone-like 2	PMCHL2	5370							
chr5	71455614	71578287	5q13	5q13.2		607012	"BDP1, TFNR"	"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB"	BDP1	55814	ENSG00000145734			Bdp1 (MGI:1347077)			
chr5	71587287	71658705	5q12-q13	5q13.2		609014	"MCCC2, MCCB"	3-Methylcrotonyl-CoA carboxylase 2	MCCC2	64087	ENSG00000131844		"3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210 (3), Autosomal recessive"	Mccc2 (MGI:1925288)			
chr5	71719162	71721047	5q13.2	5q13.2		602606	"CARTPT, CART"	Cocaine- and amphetamine-regulated transcript prepropeptide	CARTPT	9607	ENSG00000164326	mutation identified in 1 family	"{?Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Cartpt (MGI:1351330)			
chr5	72107267	72209569	5q13	5q13.2		157129	MAP1B	Microtubule-associated protein-1B	MAP1B	4131	ENSG00000131711			Map1b (MGI:1306778)			
chr5	72219408	72320256	5q13.2	5q13.2		611989	"MRPS27, KIAA0264"	Mitochondrial ribosomal protein S27	MRPS27	23107	ENSG00000113048			Mrps27 (MGI:1919064)			
chr5	72320366	72368394	5q13.2	5q13.2		615484	PTCD2	Pentatricopeptide repeat domain-containing protein 2	PTCD2	79810	ENSG00000049883			Ptcd2 (MGI:1916177)			
chr5	72439898	72507421	5q13.2	5q13.2		610159	"ZNF366, DCSCRIPT"	Zinc finger protein 366	ZNF366	167465	ENSG00000178175			Zfp366 (MGI:2178429)			
chr5	72816590	72914387	5q13.2	5q13.2		602901	"TNPO1, KPNB2, MIP1"	Transportin 1	TNPO1	3842	ENSG00000083312			Tnpo1 (MGI:2681523)			
chr5	72955980	73090521	5q13.2	5q13.2		613438	FCHO2	FCH domain-only protein 2	FCHO2	115548	ENSG00000157107			Fcho2 (MGI:3505790)			
chr5	73173195	73175142	5q13.2	5q13.2		614909	TMEM174	Transmembrane protein 174	TMEM174	134288	ENSG00000164325			Tmem174 (MGI:1915594)			
chr5	73446255	73448526	5q12-q13	5q13.2		601091	"FOXD1, FKHL8"	Forkhead box D1	FOXD1	2297	ENSG00000251493			Foxd1 (MGI:1347463)			
chr5	73552199	73565685	5q12-q13	5q13.2		605787	"ANKRA2, ANKRA"	"Ankyrin repeat-containing protein, family A, member 2"	ANKRA2	57763	ENSG00000164331			Ankra2 (MGI:1915808)			
chr5	73565740	73583376	5q13.2	5q13.2		616194	UTP15	"UTP15, U3 small nucleolar ribonucleoprotein, S. cerevisiae, homolog of"	UTP15	84135	ENSG00000164338			Utp15 (MGI:2145443)			
chr5	73626157	73941992	5q13.2	5q13.2		612790	"RGNEF, p190RHOGEF"	"Rgnef, mouse, homolog of"	ARHGEF28	64283	ENSG00000214944			Arhgef28 (MGI:1346016)			
chr5	74627405	74641423	5q13	5q13.3		605173	"ENC1, PIG10"	Ectodermal-neural cortex 1	ENC1	8507	ENSG00000171617			Enc1 (MGI:109610)			
chr5	74640022	74721287	5q13	5q13.3		606873	HEXB	"Hexosaminidase B, beta polypeptide"	HEXB	3074	ENSG00000049860		"Sandhoff disease, infantile, juvenile, and adult forms, 268800 (3), Autosomal recessive"	Hexb (MGI:96074)			
chr5	74721203	74767370	5q13	5q13.3		606544	EFG2	Elongation factor G2	GFM2	84340	ENSG00000164347			Gfm2 (MGI:2444783)			
chr5	74765428	74776911	5q13.3	5q13.3		612497	"TINP1, NSA2, HUSSY29"	Transforming growth factor-beta-inducible nuclear protein 1	NSA2	10412	ENSG00000164346			Nsa2 (MGI:1913883)			
chr5	74777573	74867993	5q13.3	5q13.3		615769	"FAM169A, SLAP75, KIAA0888"	"Family with sequence similarity 169, member A"	FAM169A	26049	ENSG00000198780			Fam169a (MGI:2444268)			
chr5	75027463	75030898	5q12	5q13.3		616782	GCNT4	"Glucosaminyl (N-acetyl) transferase 4, core 2"	GCNT4	51301	ENSG00000176928			Gcnt4 (MGI:2684919)			
chr5	75336333	75362100	5q13.3-q14	5q13.3		142910	"HMGCR, LDLCQ3"	3-hydroxy-3-methylglutaryl-Coenzyme A reductase; HMG CoA reductase	HMGCR	3156	ENSG00000113161		"[Low density lipoprotein cholesterol level QTL 3] (3); [Statins, attenuated cholesterol lowering by] (3)"	Hmgcr (MGI:96159)			
chr5	75368485	75511980	5q13.3	5q13.3		604677	"COL4A3BP, GPBP, CERT, MRD34"	COL4A3-binding protein (ceramide transporter)	COL4A3BP	10087	ENSG00000113163		"Mental retardation, autosomal dominant 34, 616351 (3), Autosomal dominant"	Col4a3bp (MGI:1915268)			
chr5	75511307	75605819	5q13.1	5q13.3		605650	"POLK, POLQ, DINB1"	"Polymerase, DNA, kappa"	POLK	51426	ENSG00000122008			Polk (MGI:1349767)			
chr5	75674197	75717487	5q13.1	5q13.3		617880	"POC5, C5orf37"	POC5 centriolar protein	POC5	134359	ENSG00000152359			Poc5 (MGI:1914713)			
chr5	75847462	76353938	5q13.3	5q13.3		610291	SV2C	Synaptic vesicle glycoprotein 2C	SV2C	22987	ENSG00000122012			Sv2c (MGI:1922459)			
chr5	76403254	76708131	5q11-q13	5q13.3		605401	IQGAP2	IQ motif-containing GTPase-activating protein-2	IQGAP2	10788	ENSG00000145703			Iqgap2 (MGI:2449975)			
chr5	76615481	76623433	5q13	5q13.3		601919	"F2RL2, PAR3"	Coagulation factor II receptor-like 2 (protease-activated receptor 3)	F2RL2	2151	ENSG00000164220	order: PAR2-PAR1-PAR3		F2rl2 (MGI:1298208)			
chr5	76716042	76735779	5q13	5q13.3		187930	"F2R, CF2R, PAR1"	Coagulation factor II (thrombin) receptor	F2R	2149	ENSG00000181104	within 900kb of GPR11		F2r (MGI:101802)			
chr5	76818976	76835314	5q13	5q13.3		600933	"F2RL1, GPR11, PAR2"	"Coagulation factor II, thrombin, receptor-like 1 (G protein-coupled receptor-11)"	F2RL1	2150	ENSG00000164251	within 900kb of F2R		F2rl1 (MGI:101910)			
chr5	76849952	76952881	5q13.3	5q13.3		610103	S100Z	"S100 calcium-binding protein, zeta"	S100Z	170591	ENSG00000171643			S100z (MGI:2685471)			
chr5	76952854	76981142	5q11.2-q13.3	5q13.3		122559	CRHBP	Corticotropin releasing hormone-binding protein	CRHBP	1393	ENSG00000145708			Crhbp (MGI:88497)			
chr5	77030384	77065233	5q13.3	5q13.3		608464	"AGGF1, VG5Q, HUS84971, FLJ10283"	Angiogenic factor with G patch and FHA domains 1	AGGF1	55109	ENSG00000164252			Aggf1 (MGI:1913799)			
chr5	77076676	77087245	5q13.3	5q13.3		615250	ZBED3	Zinc finger BED domain-containing protein 3	ZBED3	84327	ENSG00000132846			Zbed3 (MGI:1919364)			
chr5	77180251	77428255	5q13	5q13.3		603390	"PDE8B, PPNAD3, ADSD"	Phosphodiesterase 8B	PDE8B	8622	ENSG00000284762		"Pigmented nodular adrenocortical disease, primary, 3, 614190 (3); Striatal degeneration, autosomal dominant, 609161 (3), Autosomal dominant"	Pde8b (MGI:2443999)			
chr5	77426651	77620610	5q13.3	5q13.3-q14.1		617502	WDR41	WD repeat-containing protein 41	WDR41	55255	ENSG00000164253			Wdr41 (MGI:2445123)			
chr5	77600000	93000000	5q14			187260	HBT	"Telangiectasia, hereditary benign"	TELAB1	338411		max lod at D5S641	"Telangiectasia, hereditary benign, 187260 (2), Autosomal dominant"				
chr5	77600000	110200000	5q14.1-q21.3			614622	KTCN5	Keratoconus 5		100885801		between D5S2499 and D5S495	"Keratoconus 5, 614622 (2), Autosomal dominant"				
chr5	77628711	77638696	5q13.3	5q14.1		604529	OTP	"Orthopedia, Drosophila, homolog of"	OTP	23440	ENSG00000171540			Otp (MGI:99835)			
chr5	77691168	77776360	5q14.1	5q14.1		610058	TBCA	Tubulin-specific chaperone A	TBCA	6902	ENSG00000171530			Tbca (MGI:107549)			
chr5	78002325	78294754	5q14.1	5q14.1		603401	"AP3B1, ADTB3A, HPS2"	"Adaptor-related protein complex 3, beta 1 subunit (adaptin, beta-3a)"	AP3B1	8546	ENSG00000132842		"Hermansky-Pudlak syndrome 2, 608233 (3), Autosomal recessive"	Ap3b1 (MGI:1333879)			
chr5	78360502	78480738	5q13.3-q14.1	5q14.1		606911	"SCAMP1, SCAMP37"	Secretory carrier membrane protein 1	SCAMP1	9522	ENSG00000085365			Scamp1 (MGI:1349480)			
chr5	78485214	78770255	5q14.1	5q14.1		609718	"LHFPL2, KIAA0206"	LHFP-like protein 2	LHFPL2	10184	ENSG00000145685			Lhfpl2 (MGI:2145236)			
chr5	78777208	78986086	5q11-q13	5q14.1		611542	"ARSB, MPS6"	Arylsulfatase B	ARSB	411	ENSG00000113273		"Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200 (3), Autosomal recessive"	Arsb (MGI:88075)			
chr5	78997563	79069673	5q12.2-q12.3	5q14.1		605849	"DMGDH, DMGDHD"	Dimethylglycine dehydrogenase	DMGDH	29958	ENSG00000132837		"Dimethylglycine dehydrogenase deficiency, 605850 (3), Autosomal recessive"	Dmgdh (MGI:1921379)			
chr5	79069723	79090073	5q13.1-q13.2	5q14.1		605932	BHMT2	Betaine-homocysteine methyltransferase 2	BHMT2	23743	ENSG00000132840			Bhmt2 (MGI:1891379)			
chr5	79111780	79132289	5q13.1-q13.2	5q14.1		602888	BHMT	Betaine-homocysteine methyltransferase	BHMT	635	ENSG00000145692			Bhmt (MGI:1339972)			
chr5	79236101	79327214	5q13.2	5q14.1		604279	JMY	Junction-mediating and regulatory protein	JMY	133746	ENSG00000152409			Jmy (MGI:1913096)			
chr5	79373823	79513835	5q14.2	5q14.1		604798	"HOMER1, HOMER1B, HOMER1C, HOMER1A"	"Homer, homlog 1 (Drosophila)"	HOMER1	9456	ENSG00000152413			Homer1 (MGI:1347345)			
chr5	79612416	79688242	5q14.1	5q14.1		614121	"PAPD4, GLD2"	Poly(A) polymerase-associated domain-containing protein 4	PAPD4	167153	ENSG00000164329			Papd4 (MGI:2140950)			
chr5	79689338	79800225	5q12-q13	5q14.1		612193	"CMYA5, MYOSPRYN, TRIM76"	Cardiomyopathy-associated protein 5	CMYA5	202333	ENSG00000164309						
chr5	79991295	80083752	5q14.1	5q14.1		600715	THBS4	Thrombospondin IV	THBS4	7060	ENSG00000113296			Thbs4 (MGI:1101779)			
chr5	80111226	80256081	5q14.1	5q14.1		614551	"SERINC5, C5orf12, TPO1"	Serine incorporator 5	SERINC5	256987	ENSG00000164300			Serinc5 (MGI:2444223)			
chr5	80407614	80483378	5q14.1	5q14.1		608880	"ZFYVE16, ENDOFIN, KIAA0305"	Zinc finger FYVE domain-containing protein 16	ZFYVE16	9765	ENSG00000039319			Zfyve16 (MGI:2145181)			
chr5	80626225	80654980	5q11.2-q13.2	5q14.1		126060	DHFR	Dihydrofolate reductase	DHFR	1719	ENSG00000228716		"Megaloblastic anemia due to dihydrofolate reductase deficiency, 613839 (3), Autosomal recessive"	Dhfr (MGI:94890)			
chr5	80654647	80876814	5q11-q12	5q14.1		600887	"MSH3, FAP4"	"mutS, E. coli, homolog of, 3"	MSH3	4437	ENSG00000113318	5' to DHFR	"Endometrial carcinoma, somatic, 608089 (3); Familial adenomatous polyposis 4, 617100 (3), Autosomal recessive"	Msh3 (MGI:109519)			
chr5	80960671	81230161	5q13	5q14.1		606614	RASGRF2	Ras protein-specific guanine nucleotide-releasing factor 2	RASGRF2	5924	ENSG00000113319			Rasgrf2 (MGI:109137)			
chr5	81227594	81266397	5q13.3	5q14.1		123295	CKMT2	"Creatine kinase, mitochondrial-2 (sarcomeric)"	CKMT2	1160	ENSG00000131730			Ckmt2 (MGI:1923972)			
chr5	81309044	81394173	5q14.1	5q14.1		614315	"ACOT12, CACH"	Acyl-CoA thioesterase 12	ACOT12	134526	ENSG00000172497			Acot12 (MGI:1921406)			
chr5	81412806	81751252	5q13.3	5q14.1		607389	SSBP2	Single-stranded DNA-binding protein 2	SSBP2	23635	ENSG00000145687			Ssbp2 (MGI:1914220)			
chr5	81972020	82258501	5q14.2	5q14.1-q14.2		610800	"ATG10, APG10"	"Autophagy 10, S. cerevisiae, homolog of"	ATG10	83734	ENSG00000152348			Atg10 (MGI:1914045)			
chr5	82100000	83500000	5q14.2			614317	VUR4	Vesicoureteral reflux 4		100820757		closest marker rs1501656	"Vesicoureteral reflux 4, 614317 (2)"				
chr5	82273319	82278415	5q14.2	5q14.2		603683	"RPS23, BTDD, MCINS"	Ribosomal protein S23	RPS23	6228	ENSG00000186468		"Brachycephaly, trichomegaly, and developmental delay, 617412 (3), Autosomal dominant"	Rps23 (MGI:1913725)			
chr5	83064203	83064336	5q14.2	5q14.2		611329	SCARNA18	Small cajal body-specific RNA 18	SCARNA18	677765		in intron 1 of TMEM167					
chr5	83077408	83370332	5q13-q14	5q14.2		194363	"XRCC4, SSMED"	"X-ray repair, complementing defective, repair in Chinese hamster cells-4"	XRCC4	7518	ENSG00000152422	between D5S427 and D5S401	"Short stature, microcephaly, and endocrine dysfunction, 616541 (3), Autosomal recessive"	Xrcc4 (MGI:1333799)			
chr5	83471673	83582302	5q12-q14	5q14.2-q14.3		118661	"VCAN, CSPG2, WGN, WGN1, ERVR"	Versican (chondroitin sulfate proteoglycan-2)	VCAN	1462	ENSG00000038427		"Wagner syndrome 1, 143200 (3), Autosomal dominant"	Vcan (MGI:102889)			
chr5	83500000	98900000	5q14.3-q15			612881	PVNH5	Periventricular nodular heterotopia 5				"deletion range 6.3-17Mb, common range 5.8Mb"	"Periventricular nodular heterotopia 5, 612881 (4)"				
chr5	83638197	83721209	5q13-q14.1	5q14.3		115435	"HAPLN1, CRTL1"	Hyaluronan and proteoglycan link protein 1	HAPLN1	1404	ENSG00000145681			Hapln1 (MGI:1337006)			
chr5	86617966	86620765	5q14	5q14.3		603774	COX7C	"Cytochrome C oxidase, subunit VII C"	COX7C	1350	ENSG00000127184	pseudogene on 13q14-q21					
chr5	87267844	87391925	5q13.3	5q14.3		139150	"RASA1, GAP, CMAVM, PKWS"	RAS p21 protein activator 1 (GTPase activating protein)	RASA1	5921	ENSG00000145715		"Basal cell carcinoma, somatic, 605462 (3); Capillary malformation-arteriovenous malformation, 608354 (3), Autosomal dominant; Parkes Weber syndrome, 608355 (3), Autosomal dominant"	Rasa1 (MGI:97860)			
chr5	87311479	87413032	5q13.3-q14	5q14.3		601953	"CCNH, CAK"	Cyclin H	CCNH	902	ENSG00000134480			Ccnh (MGI:1913921)			
chr5	88538265	88691040	5q14.3	5q14.3		616611	"LINC00461, VISC"	Long intergenic noncoding RNA 461	LINC00461	645323							
chr5	88666852	88666938	5q14.3	5q14.3		611187	"MIR9-2, MIRN9-2"	Micro RNA 9-2	MIR9-2	407047							
chr5	88718240	88904104	5q14	5q14.3		600662	"MEF2C, C5DELq14.3, DEL5q14.3"	"MADS box transcription enhancer factor 2, polypeptide C (myocyte enhancer factor 2C)"	MEF2C	4208	ENSG00000081189		"Chromosome 5q14.3 deletion syndrome, 613443 (4), Autosomal dominant; Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations, 613443 (3), Autosomal dominant"	Mef2c (MGI:99458)			
chr5	90393334	90409785	5q14.3	5q14.3		602907	"CETN3, CDC31"	Centrin 3	CETN3	1070	ENSG00000153140			Cetn3 (MGI:1097706)			
chr5	90473928	90514554	5p14.3	5q14.3		617456	"POLR3G, RPC32, RPC7"	"Polymerase III, RNA, subunit G"	POLR3G	10622	ENSG00000113356			Polr3g (MGI:1914736)			
chr5	90558795	91164225	5q14.3	5q14.3		602851	"ADGRV1, GPR98, MASS1, VLGR1, KIAA0686, FEB4, USH2C"	Adhesion G protein-coupled receptor V1	ADGRV1	84059	ENSG00000164199	mutation identified in 1 FEB4 family	"?Febrile seizures, familial, 4, 604352 (3), Autosomal dominant; Usher syndrome, type 2C, 605472 (3), Autosomal recessive; Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472 (3), Autosomal recessive"	Adgrv1 (MGI:1274784)			
chr5	91368631	91383372	5q14.3	5q14.3		612464	"ARRDC3, TLIMP, KIAA1376"	Arrestin domain-containing 3	ARRDC3	57561	ENSG00000113369			Arrdc3 (MGI:2145242)			
chr5	93583336	93594612	5q14	5q15		132890	"NR2F1, TFCOUP1, ERBAL3, EAR3, BBSOAS"	"Nuclear receptor subfamily 2, group F, member 1 (transcription factor COUP 1)"	NR2F1	7025	ENSG00000175745		"Bosch-Boonstra-Schaaf optic atrophy syndrome, 615722 (3), Autosomal dominant"	Nr2f1 (MGI:1352451)			
chr5	94150850	94618603	5q15	5q15		617266	KIAA0825	KIAA0825 gene	KIAA0825	285600	ENSG00000185261			2210408I21Rik (MGI:1919621)			
chr5	94703689	95284574	5q15	5q15		616296	MCTP1	Multiple C2 domains-containing transmembrane protein 1	MCTP1	79772	ENSG00000175471			Mctp1 (MGI:1926021)			
chr5	95463894	95555004	5q15	5q15		614589	"TTC37, KIAA0372"	Tetratricopeptide repeat domain 37	TTC37	9652	ENSG00000198677		"Trichohepatoenteric syndrome 1, 222470 (3), Autosomal recessive"	Ttc37 (MGI:2679923)			
chr5	95555107	95605101	5q15	5q15		610011	ARSK	Arylsulfatase K	ARSK	153642	ENSG00000164291			Arsk (MGI:1924291)			
chr5	95713521	95796366	5q14.3	5q15		607353	"RHOBTB3, KIAA0878"	Rho-related BTB domain-containing protein 3	RHOBTB3	22836	ENSG00000164292			Rhobtb3 (MGI:1920546)			
chr5	95813848	95822872	5q14	5q15		600443	"GLRX, GRX"	Glutaredoxin (thioltransferase)	GLRX	2745	ENSG00000173221			Glrx (MGI:2135625)			
chr5	95885097	95962070	5q15	5q15		601874	ELL2	"Elongation factor, RNA polymerase II, 2"	ELL2	22936	ENSG00000118985			Ell2 (MGI:2183438)			
chr5	96390335	96433280	5q15-q21	5q15		162150	"PCSK1, NEC1, PC1, PC3, BMIQ12"	Proprotein convertase subtilisin/kexin type 1	PCSK1	5122	ENSG00000175426		"Obesity with impaired prohormone processing, 600955 (3), Autosomal recessive; {Obesity, susceptibility to, BMIQ12}, 612362 (3)"	Pcsk1 (MGI:97511)			
chr5	96662036	96774682	5q15-q21	5q15		114090	"CAST, PLACK"	Calpastatin	CAST	831	ENSG00000153113		"Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads, 616295 (3), Autosomal recessive"	Cast (MGI:1098236)			
chr5	96760272	96935982	5q15	5q15		606832	"ERAP1, ALAP, ARTS1, PILSAP, KIAA0525"	Endoplasmic reticulum aminopeptidase 1	ERAP1	51752	ENSG00000164307			Erap1 (MGI:1933403)			
chr5	96875938	96919715	5q15	5q15		609497	"ERAP2, LRAP"	Endoplasmic reticulum aminopeptidase 2	ERAP2	64167	ENSG00000164308						
chr5	96934858	97037512	5q14.2-q15	5q15		151300	LNPEP	Leucyl-cystinyl aminopeptidase	LNPEP	4012	ENSG00000113441			Lnpep (MGI:2387123)			
chr5	97091869	97142815	5q15	5q15		610466	LIX1	"Limb expression 1, mouse, homolog of"	LIX1	167410	ENSG00000145721			Lix1 (MGI:1913893)			
chr5	97160866	97183300	5q15	5q15		617754	"RIOK2, RIO2"	RIO kianse 2	RIOK2	55781	ENSG00000058729			Riok2 (MGI:1914295)			
chr5	98768385	98796493	5q21.1	5q15		612687	"RGMB, DRAGON"	"RGM domain family, member B"	RGMB	285704	ENSG00000174136			Rgmb (MGI:1916049)			
chr5	98855203	98929771	5q15-q21	5q15-q21		602118	"CHD1, PILBOS"	Chromodomain helicase DNA binding protein-1	CHD1	1105	ENSG00000153922		"Pilarowski-Bjornsson syndrome, 617682 (3), Autosomal dominant"	Chd1 (MGI:88393)			
chr5	98900000	110200000	5q21			609570	MGR8	"Migraine, susceptibility to, 8"		100188790			"{Migraine, susceptibility to, 8}, 609570 (2)"				
chr5	100806934	100903284	5q21	5q21.1		602547	"PST, PST1"	Polysialyltransferase	ST8SIA4	7903	ENSG00000113532			St8sia4 (MGI:106018)			
chr5	102233985	102296548	5q21.1	5q21.1		609013	"SLCO4C1, OATP4C1"	"Solute carrier organic anion transporter family, member 4C1"	SLCO4C1	353189	ENSG00000173930			Slco4c1 (MGI:2442784)			
chr5	102371781	102502212	5q21.1	5q21.1		613365	"SLCO6A1, GST"	"Solute carrier organic anion transporter family, member 6A1"	SLCO6A1	133482	ENSG00000205359			Slco6b1 (MGI:1915104)			
chr5	102754782	103031104	5q14-q21	5q21.1		170270	PAM	Peptidylglycine alpha-amidating monooxygenase	PAM	5066	ENSG00000145730			Pam (MGI:97475)			
chr5	103120247	103204910	5q21.1	5q21.1		611648	"HISPPD1, PPIP5K2, VIP2, KIAA0433"	Histidine acid phosphatase domain-containing protein 1	PPIP5K2	23262	ENSG00000145725			Ppip5k2 (MGI:2142810)			
chr5	103258701	103278659	5q21.1	5q21.1		616608	C5orf30	Chromosome 5 open reading frame 30	C5orf30	90355	ENSG00000181751			D1Ertd622e (MGI:1277184)			
chr5	105100000	156300000	5q21.3-q33.2			608970	MDBS2	"Macular dystrophy, butterfly-shaped pigmentary, 2"				between D5S433 and D5S410	"Macular dystrophy, butterfly-shaped pigmentary, 2, 608970 (2), Autosomal dominant"				
chr5	107376888	107670894	5q21.3	5q21.3		601535	"EFNA5, EPLG7, LERK7"	Ephrin A5	EFNA5	1946	ENSG00000184349			Efna5 (MGI:107444)			
chr5	107859032	108382097	5q21.3	5q21.3		609083	"FBXL17, FBL17, FBX13, FBXO13"	F-box and leucine-rich repeat protein 17	FBXL17	64839	ENSG00000145743			Fbxl17 (MGI:1354704)			
chr5	108593483	108594002	5q13-q23	5q21.3		180463	RPS20A	Ribosomal protein S20A	RPS20P3	6225		?pseudogene					
chr5	108746084	109196840	5q21-q22	5q21.3		176942	"FER, TYK3"	fer (fps/fes related) tyrosine kinase	FER	2241	ENSG00000151422			Fer (MGI:105917)			
chr5	109689365	109869624	5q21-q22	5q21.3		154582	"MAN2A1, MANA2"	"Mannosidase, alpha, class 2A, member 1"	MAN2A1	4124	ENSG00000112893			Man2a1 (MGI:104669)			
chr5	110200000	115900000	5q22			613412	EOE2	"Esophagitis, eosinophilic, 2"		100499167		association with rs3806932	"{Esophagitis, eosinophilic, 2}, 613412 (2), Multifactorial"				
chr5	110200000	150400000	5q22.1-q32			610535	GLC1M	"Glaucoma 1, open angle, M"	GLC1M	777643		between D5S2051 and D5S2090	"Glaucoma 1, open angle, M, 610535 (2), Autosomal dominant"				
chr5	110738135	110765173	5q22.1	5q22.1		610826	"SLC25A46, HMSN6B"	"Solute carrier family 25, member 46"	SLC25A46	91137	ENSG00000164209		"Neuropathy, hereditary motor and sensory, type VIB, 616505 (3), Autosomal recessive"	Slc25a46 (MGI:1914703)			
chr5	111070079	111078023	5q22.1	5q22.1		607003	TSLP	Thymic stromal lymphopoietin	TSLP	85480	ENSG00000145777			Tslp (MGI:1855696)			
chr5	111092171	111130501	5q21.3-q22.1	5q22.1		609669	"WDR36, TAWDRP, GLC1G"	WD repeat-containing protein 36	WDR36	134430	ENSG00000134987		"Glaucoma 1, open angle, G, 609887 (3)"	Wdr36 (MGI:1917819)			
chr5	111223652	111498502	5q21-q23	5q22.1		114080	CAMK4	Ca(2+)-calmodulin-dependent protein kinase type IV of brain	CAMK4	814	ENSG00000152495			Camk4 (MGI:88258)			
chr5	111491421	111512596	5q22	5q22.1		607049	STARD4	Start domain-containing protein 4	STARD4	134429	ENSG00000164211			Stard4 (MGI:2156764)			
chr5	111729302	111976930	5q22.1	5q22.1		607332	"C5orf13, P311, PTZ17"	P311 protein	NREP	9315	ENSG00000134986			Nrep (MGI:99444)			
chr5	112141828	112419315	5q22	5q22.1-q22.2		612141	"EPB41L4A, EPB41L4, NBL4"	Erythrocyte membrane protein band 4.1-like 4A	EPB41L4A	64097	ENSG00000129595			Epb41l4a (MGI:103007)			
chr5	112707504	112846238	5q22.2	5q22.2		611731	"APC, GS, FPC, BTPS2"	Adenomatous polyposis coli	APC	324	ENSG00000134982	150kb distal to MCC	"Adenoma, periampullary, somatic (3); Adenomatous polyposis coli, 175100 (3), Autosomal dominant; Brain tumor-polyposis syndrome 2, 175100 (3), Autosomal dominant; Colorectal cancer, somatic, 114500 (3); Desmoid disease, hereditary, 135290 (3), Autosomal dominant; Gardner syndrome, 175100 (3), Autosomal dominant; Gastric cancer, somatic, 613659 (3); Hepatoblastoma, somatic, 114550 (3)"	Apc (MGI:88039)			
chr5	112861187	112893078	5q21-q22	5q22.2		182175	SRP19	Signal recognition particle 19kD	SRP19	6728	ENSG00000153037	within 100kb of APC		Srp19 (MGI:1913634)			
chr5	112876383	112922333	5q22-q23	5q22.2		125265	"REEP5, D5S346, DP1, C5orf18"	Receptor expression-enhancing protein 5	REEP5	7905	ENSG00000129625			Reep5 (MGI:1270152)			
chr5	112891615	112893096	5q22	5q22.2		601079	"ZRSR1, U2AF1RS1"	"Zinc finger-, CCCH domain-, and RNA-binding motif-containing serine/arginine-rich protein 1"	ZRSR2P1	7310							
chr5	112976701	113022194	5q21-q22	5q22.2		609844	DCP2	"Decapping enzyme 2, S. cerevisiae, homolog of"	DCP2	167227	ENSG00000172795			Dcp2 (MGI:1917890)			
chr5	113022098	113488829	5q21	5q22.2		159350	MCC	Mutated in colorectal cancers	MCC	4163	ENSG00000171444		"Colorectal cancer, somatic, 114500 (3)"	Mcc (MGI:96930)			
chr5	113432553	113435030	5q22.2	5q22.2		610709	"TSSK1, STK22D"	Testis-specific serine/threonine kinase 1	TSSK1B	83942	ENSG00000212122	pseudogene on chr22		Tssk1 (MGI:1347557)			
chr5	113513661	113595286	5q22.2	5q22.2		616530	"YTHDC2, CAHL"	YTH domain-containing protein 2	YTHDC2	64848	ENSG00000047188			Ythdc2 (MGI:2448561)			
chr5	114056005	114496499	5q21.2-q22.1	5q22.3		605879	"KCNN2, SK2"	"Potassium channel, calcium-activated, intermediate/small conductance, subfamily N, member 2"	KCNN2	3781	ENSG00000080709						
chr5	115124761	115180545	5q22.3	5q22.3		609317	"TRIM36, RBCC728, ANPH"	Tripartite motif-containing protein 36	TRIM36	55521	ENSG00000152503	mutation identified in 1 ANPH patient	"?Anencephaly, 206500 (3), Autosomal recessive"	Trim36 (MGI:106264)			
chr5	115200246	115262886	5q22.3	5q22.3		602031	PGGT1B	"Protein geranylgeranyltransferase type I, beta subunit"	PGGT1B	5229	ENSG00000164219			Pggt1b (MGI:1917514)			
chr5	115578495	115602478	5q23.1	5q22.3		608321	"TIRP, TRAM"	Toll/interleukin-1 receptor domain-containing protein	TICAM2	353376	ENSG00000243414			Ticam2 (MGI:3040056)			
chr5	115804732	115816707	5q22-q23	5q22.3		603943	CDO1	"Cysteine dioxygenase, type 1"	CDO1	1036	ENSG00000129596			Cdo1 (MGI:105925)			
chr5	115841605	115914080	5q23.1	5q22.3-q23.1		601507	"AP3S1, CLAPS3"	"Adaptor-related protein complex 3, sigma 1 subunit"	AP3S1	1176	ENSG00000177879	previously assigned to chr. 12 by FISH		Ap3s1 (MGI:1337062)			
chr5	115900000	181538259	5q23-q35			181510	SCZD1	"Schizophrenia susceptibility locus, chromosome 5-related"	SCZD1	6377		max lod at D5S820	"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr5	115962453	116027601	5q23.1	5q23.1		610046	LVRN	Laeverin	LVRN	206338	ENSG00000172901			Lvrn (MGI:1921824)			
chr5	116084975	116447434	5q23.1	5q23.1		616704	COMMD10	COMM domain-containing protein 10	COMMD10	51397	ENSG00000145781			Commd10 (MGI:1916706)			
chr5	116443554	116574925	5q23.1	5q23.1		605885	SEMA6A	Semaphorin 6A	SEMA6A	57556	ENSG00000092421			Sema6a (MGI:1203727)			
chr5	119071001	119249431	5q21-q22	5q23.1		605671	DMXL1	DMX-like 1	DMXL1	1657	ENSG00000172869			Dmxl1 (MGI:2443926)			
chr5	119268691	119394603	5q23.1	5q23.1		612111	"TNFAIP8, SCCS2"	Tumor necrosis factor-alpha-induced protein 8	TNFAIP8	25816	ENSG00000145779			Tnfaip8 (MGI:2147191)			
chr5	119452442	119542334	5q23.1	5q23.1		601860	"HSD17B4, PRLTS1"	Hydroxysteroid (17-beta) dehydrogenase 4	HSD17B4	3295	ENSG00000133835		"D-bifunctional protein deficiency, 261515 (3), Autosomal recessive; Perrault syndrome 1, 233400 (3), Autosomal recessive"	Hsd17b4 (MGI:105089)			
chr5	120464221	120794586	5q23.1	5q23.1		615931	"PRR16, LARGEN"	Proline-rich protein 16	PRR16	51334	ENSG00000184838			Prr16 (MGI:1918623)			
chr5	121851954	121852832	5q21.3	5q23.1		608847	FTMT	"Ferritin, mitochondrial"	FTMT	94033	ENSG00000181867			Ftmt (MGI:1914884)			
chr5	121961960	122075623	5q23.1	5q23.1		610479	"SRFBP1, P49"	Serum response factor binding protein 1	SRFBP1	153443	ENSG00000151304			Srfbp1 (MGI:1914472)			
chr5	122063194	122078500	5q23.3-q31.2	5q23.1		153455	"LOX, AAT10"	Lysyl oxidase	LOX	4015	ENSG00000113083		"Aortic aneurysm, familial thoracic 10, 617168 (3), Autosomal dominant"	Lox (MGI:96817)			
chr5	122311353	122464218	5q23.1-q23.3	5q23.2		603779	SNCAIP	Synuclein-alpha-interacting protein (synphilin 1)	SNCAIP	9627	ENSG00000064692			Sncaip (MGI:1915097)			
chr5	122774995	122834538	5q23	5q23.2		605929	SNX2	Sorting nexin 2	SNX2	6643	ENSG00000205302			Snx2 (MGI:1915054)			
chr5	123023382	123036729	5q23.2	5q23.2		123842	PPIC	Peptidyl-prolyl isomerase C	PPIC	5480	ENSG00000168938			Ppic (MGI:97751)			
chr5	123089102	123194265	5q23.2	5q23.2		616982	"PRDM6, PRISM, PDA3"	PR domain-containing protein 6	PRDM6	93166	ENSG00000061455		"Patent ductus arteriosus 3, 617039 (3), Autosomal dominant"	Prdm6 (MGI:2684938)			
chr5	123344884	123423591	5q23.2	5q23.2		613446	"CEP120, CCDC100, SRTD13, JBTS31"	"Centrosomal protein, 120kD"	CEP120	153241	ENSG00000168944		"Joubert syndrome 31, 617761 (3), Autosomal recessive; Short-rib thoracic dysplasia 13 with or without polydactyly, 616300 (3), Autosomal recessive"	Cep120 (MGI:2147298)			
chr5	123512098	123617044	5q23	5q23.2		604253	CSNK1G3	"Casein kinase I, gamma-3"	CSNK1G3	1456	ENSG00000151292			Csnk1g3 (MGI:1917675)			
chr5	126541840	126595389	5q31	5q23.2		107323	"ALDH7A1, ATQ1, EPD, PDE"	"Aldehyde dehydrogenase 7 family, member A1 (antiquitin 1)"	ALDH7A1	501	ENSG00000164904		"Epilepsy, pyridoxine-dependent, 266100 (3), Autosomal recessive"	Aldh7a1 (MGI:108186)			
chr5	126600914	126627251	5q23.2	5q23.2		604924	"RNUXA, PHAX"	"RNA, U small nuclear, export adaptor"	PHAX	51808	ENSG00000164902			Phax (MGI:1891839)			
chr5	126776622	126837019	5q23.2	5q23.2		150340	"LMNB1, ADLD"	Lamin B1	LMNB1	4001	ENSG00000113368		"Leukodystrophy, adult-onset, autosomal dominant, 169500 (3), Autosomal dominant"	Lmnb1 (MGI:96795)			
chr5	126867713	127032401	5q23.2	5q23.2		613333	3-Mar	Membrane-associated RING-CH finger protein 3	3-Mar	115123	ENSG00000173926			March3 (MGI:2443667)			
chr5	127229518	127461221	5q23.2	5q23.2		612453	"MEGF10, KIAA1780, EMARDD"	Multiple epidermal growth factor-like domains 10	MEGF10	84466	ENSG00000145794		"Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399 (3), Autosomal recessive; Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant, 614399 (3), Autosomal recessive"	Megf10 (MGI:2685177)			
chr5	128083790	128189687	5q23.3	5q23.3		600840	"SLC12A2, NKCC1"	"Solute carrier family 12 (sodium/potassium/chloride transporters), member 2"	SLC12A2	6558	ENSG00000064651			Slc12a2 (MGI:101924)			
chr5	128257908	128538041	5q23-q31	5q23.3		612570	"FBN2, CCA, EOMD"	Fibrillin-2	FBN2	2201	ENSG00000138829		"Contractural arachnodactyly, congenital, 121050 (3), Autosomal dominant; Macular degeneration, early-onset, 616118 (3), Autosomal dominant"	Fbn2 (MGI:95490)			
chr5	129460264	129738682	5q31	5q23.3		607513	ADAMTS19	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 19"	ADAMTS19	171019	ENSG00000145808			Adamts19 (MGI:2442875)			
chr5	129903383	130186636	5q31	5q23.3		609963	"CHSY3, CSS3"	Chondroitin sulfate synthase 3	CHSY3	337876	ENSG00000198108			Chsy3 (MGI:1926173)			
chr5	131159282	131165347	5q31.2	5q23.3		601314	"HINT1, PRKCNH1, NMAN"	Histidine triad nucleotide-binding protein 1 (protein kinase C inhibitor 1)	HINT1	3094	ENSG00000169567		"Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 (3), Autosomal recessive"	Hint1 (MGI:1321133)			
chr5	131170913	131205425	5q23.3	5q23.3-q31.1		615831	"LYRM7, MZM1L, MC3DN8"	LYR motif-containing protein 7	LYRM7	90624	ENSG00000186687		"Mitochondrial complex III deficiency, nuclear type 8, 615838 (3), Autosomal recessive"	Lyrm7 (MGI:1922780)			
chr5	131200000	160500000	5q31-q33			608174	AITD2	"Autoimmune thyroid disease, susceptibility to, 2"		387579			"{Autoimmune thyroid disease, susceptibility to, 2}, 608174 (2)"				
chr5	131200000	160500000	5q31-q33			605845	ATOD6	"Dermatitis, atopic, 6"		114477		between D5S436 and D5S643	"{Dermatitis, atopic, susceptibility to, 6}, 605845 (2)"				
chr5	131200000	160500000	5q31-q33			609754	CELIAC2	"Celiac disease, susceptibility to, 2"	CELIAC2	317782			"{Celiac disease, susceptibility to, 2}, 609754 (2)"				
chr5	131200000	150400000	5q31.1-q32			607683	"DFNA52, DFNA42"	"Deafness, autosomal dominant 52"				max lod at D5S2017	"Deafness, autosomal dominant 52, 607683 (2), Autosomal dominant"				
chr5	131200000	145100000	5q31			615649	DFNA54	"Deafness, autosomal dominant 54"	DFNA54	448962		between D5S1972 and D5S410	"Deafness, autosomal dominant 54, 615649 (2), Autosomal dominant"				
chr5	131200000	160500000	5q31-q33			131400	EOS	"Eosinophilia, familial"		7908			"Eosinophilia, familial, 131400 (2), Autosomal dominant"				
chr5	131200000	145100000	5q31			606348	IBD5	Inflammatory bowel disease 5	IBD5	50941			"{Inflammatory bowel disease 5}, 606348 (2)"				
chr5	131200000	153300000	5q31.1-q33.1			605598	IDDM18	Insulin-dependent diabetes mellitus-18	IDDM18	57044		close to IL12B	"{Diabetes mellitus, insulin-dependent, 18}, 605598 (2)"				
chr5	131200000	136900000	5q31.1			147061	IGES	"Immunoglobulin E concentration, serum"	IGES	3478			"{?Allergy and asthma susceptibility}, 147061 (2)"				
chr5	131200000	145100000	5q31			604966	PCDHA@	Protocadherin-alpha gene cluster									
chr5	131200000	145100000	5q31			604967	PCDHB@	Protocadherin-beta gene cluster									
chr5	131200000	145100000	5q31			604968	PCDHG	Protocadherin-gamma gene cluster									
chr5	131200000	145100000	5q31			606263	PDB4	Paget disease of bone 4	PDB4	94003			"Paget disease of bone 4, 606263 (2), Autosomal dominant"				
chr5	131200000	160500000	5q31-q33			248310	PFBI	Plasmodium falciparum blood infection levels		7910			"{Malaria, intensity of infection}, 248310 (2), Autosomal recessive"				
chr5	131200000	153300000	5q31.1-q33.1			612599	PSORS11	Psoriasis susceptibility 11		100271719		associated with rs10045431	"{Psoriasis susceptibility 11}, 612599 (2)"				
chr5	131200000	145100000	5q31			615197	RLS8	"Restless legs syndrome, susceptibility to, 8"		101448072			"{Restless legs syndrome 8}, 615197 (2)"				
chr5	131200000	160500000	5q31-q33			181460	SM1	"Schistosoma mansoni infection, susceptibility/resistance to"		7911			"{Schistosoma mansoni infection, susceptibility/resistance to}, 181460 (2), Autosomal dominant"				
chr5	131423920	131635235	5q31.1	5q31.1		610499	"RAPGEF6, RAGEF2, PDZGEF2"	RAP guanine nucleotide exchange factor 6	RAPGEF6	51735	ENSG00000158987			Rapgef6 (MGI:2384761)			
chr5	131641712	131797062	5q23.3	5q31.1		610594	"FNIP1, KIAA1961"	Folliculin-interacting protein 1	FNIP1	96459	ENSG00000217128			Fnip1 (MGI:2444668)			
chr5	131806989	131945697	5q31.1	5q31.1		616232	MEIKIN	Meiotic kinetochore factor	MEIKIN	728637	ENSG00000239642			Meikin (MGI:1922097)			
chr5	131949972	132012067	5q31	5q31.1		604443	"ACSL6, FACL6, ACS2"	Acyl-CoA synthetase long-chain family member 6	ACSL6	23305	ENSG00000164398		"Myelodysplastic syndrome (3); Myelogenous leukemia, acute (3)"	Acsl6 (MGI:894291)			
chr5	132060653	132063202	5q31.1	5q31.1		147740	IL3	Interleukin-3	IL3	3562	ENSG00000164399	9kb from CSF2; order: cen-5'IL3-5'CF2-qter					
chr5	132073791	132076169	5q31.1	5q31.1		138960	"CSF2, GMCSF"	Colony-stimulating factor-2 (granulocyte-macrophage)	CSF2	1437	ENSG00000164400	order: cen-CSF2-CSF1-FMS-qter		Csf2 (MGI:1339752)			
chr5	132190146	132227862	5q31	5q31.1		600608	"P4HA2, MYP25"	"Procollagen-proline, 2-oxoglutarate-4-dioxygenase, alpha subunit, isoform 2"	P4HA2	8974	ENSG00000072682		"Myopia 25, autosomal dominant, 617238 (3), Autosomal dominant"	P4ha2 (MGI:894286)			
chr5	132257657	132273453	5q31.1	5q31.1		603422	RIL	LIM domain protein ril	PDLIM4	8572	ENSG00000131435		"{Osteoporosis, susceptibility to}, 166710 (3), Autosomal dominant"	Pdlim4 (MGI:1353470)			
chr5	132294383	132344205	5q31	5q31.1		604190	"SLC22A4, OCTN1"	"Solute carrier family 22 (organic cation transporter), member 4"	SLC22A4	6583	ENSG00000197208		"{Rheumatoid arthritis, susceptibility to}, 180300 (3)"	Slc22a4 (MGI:1353479)			
chr5	132369703	132395613	5q31.1	5q31.1		603377	"SLC22A5, OCTN2, CDSP, SCD"	"Solute carrier, family 22 (organic cation transporter), member 5"	SLC22A5	6584	ENSG00000197375		"Carnitine deficiency, systemic primary, 212140 (3), Autosomal recessive"	Slc22a5 (MGI:1329012)			
chr5	132481608	132490788	5q31.1	5q31.1		147575	"IRF1, MAR"	Interferon regulatory factor-1	IRF1	3659	ENSG00000125347		"Gastric cancer, somatic, 613659 (3); Myelodysplastic syndrome, preleukemic (3); Myelogenous leukemia, acute (3); Nonsmall cell lung cancer, somatic, 211980 (3)"	Irf1 (MGI:96590)			
chr5	132539193	132556863	5q31.1	5q31.1		147850	IL5	Interleukin-5	IL5	3567	ENSG00000113525	< 310kb from IL4		Il5 (MGI:96557)			
chr5	132556923	132644620	5q31	5q31.1		604040	"RAD50, NBSLD"	"RAD50, S. cerevisiae, homolog of"	RAD50	10111	ENSG00000113522		"Nijmegen breakage syndrome-like disorder, 613078 (3)"	Rad50 (MGI:109292)			
chr5	132656523	132661108	5q31	5q31.1		147683	"IL13, ALRH, BHR1"	Interleukin-13	IL13	3596	ENSG00000169194		"{Allergic rhinitis, susceptibility to}, 607154 (3); {Asthma, susceptibility to}, 600807 (3), Autosomal dominant"	Il13 (MGI:96541)			
chr5	132673985	132682677	5q31.1	5q31.1		147780	IL4	Interleukin-4	IL4	3565	ENSG00000113520			Il4 (MGI:96556)			
chr5	132688807	132737577	5q31	5q31.1		604683	KIF3A	Kinesin family member 3A	KIF3A	11127	ENSG00000131437			Kif3a (MGI:107689)			
chr5	132750816	132778215	5q31-q33	5q31.1		608418	"SEPT8, KIAA0202"	Septin 8	8-Sep	23176	ENSG00000164402			Sept8 (MGI:894310)			
chr5	132822140	132831626	5q31.1	5q31.1		611179	"SHROOM1, APXL2, KIAA1960"	SHROOM family member 1	SHROOM1	134549	ENSG00000164403			Shroom1 (MGI:1919024)			
chr5	132861180	132866883	5q31.1	5q31.1		601918	GDF9	Growth/differentiation factor 9	GDF9	2661	ENSG00000164404			Gdf9 (MGI:95692)			
chr5	132866626	132868843	5q31.1	5q31.1		612080	"UQCRQ, QPC, MC3DN4"	"Ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kD"	UQCRQ	27089	ENSG00000164405		"Mitochondrial complex III deficiency, nuclear type 4, 615159 (3), Autosomal recessive"	Uqcrq (MGI:107807)			
chr5	132873665	132874889	5q31.1	5q31.1		611373	LEAP2	Liver-expressed antimicrobial peptide 2	LEAP2	116842	ENSG00000164406			Leap2 (MGI:2672795)			
chr5	132875378	132963661	5q31	5q31.1		604417	"AFF4, AF5Q31, CHOPS"	"AF4/FMR2 family, member 4"	AFF4	27125	ENSG00000072364		"CHOPS syndrome, 616368 (3), Autosomal dominant"	Aff4 (MGI:2136171)			
chr5	133051969	133105016	5q31.1-q31.2	5q31.1		601113	HSPA4	Heat-shock 70kD protein-4	HSPA4	3308	ENSG00000170606			Hspa4 (MGI:1342292)			
chr5	133913676	133917268	5q31.1	5q31.1		616333	"WSPAR, lncTCF7"	WNT signaling pathway activating noncoding RNA	WSPAR	105664404							
chr5	133971874	134070986	5q31	5q31.1		604492	VDAC1	Voltage-dependent anion channel 1	VDAC1	7416	ENSG00000213585			Vdac1 (MGI:106919)			
chr5	134114697	134148228	5q31.1	5q31.1		189908	TCF7	"Transcription factor-7, T-cell specific"	TCF7	6932	ENSG00000081059	originally called TCF-1					
chr5	134156390	134177032	5q31	5q31.1		601434	"SKP1, SKP1A, TCEB1L, OCP2"	S-phase kinase-associated protein 1 (p19A)	SKP1	6500	ENSG00000113558	pseudogene on chr.7		Skp1a (MGI:103575)			
chr5	134196251	134226258	5q23-q31	5q31.1		176915	PPP2CA	"Protein phosphatase-2 (formerly 2A), catalytic subunit, alpha isoform"	PPP2CA	5515	ENSG00000113575			Ppp2ca (MGI:1321159)			
chr5	134236119	134372379	5q31	5q31.1		608459	"CDKL3, NKIAMRE"	Cyclin-dependent kinase-like 3	CDKL3	51265	ENSG00000006837			Cdkl3 (MGI:2388268)			
chr5	134371175	134392107	5q23-q31	5q31.1		179095	"UBE2B, RAD6B"	Ubiquitin-conjugating enzyme E2B (RAD6 homolog)	UBE2B	7320	ENSG00000119048		?Male infertility (1)	Ube2b (MGI:102944)			
chr5	134524152	134583229	5q31.1	5q31.1		610515	"PHF15, JADE2, KIAA0239"	PHD finger protein 15	JADE2	23338	ENSG00000043143			Jade2 (MGI:1924151)			
chr5	134601148	134632842	5q31.1	5q31.1		607690	"SAR1B, CMRD, SARA2, ANDD"	"Sar1a, S. cerevisiae, homolog 2"	SAR1B	51128	ENSG00000152700		"Chylomicron retention disease, 246700 (3), Autosomal recessive"	Sar1b (MGI:1913647)			
chr5	134647756	134727910	5q31.1	5q31.1		607183	SEC24A	"Sec24-related gene family, member A"	SEC24A	10802	ENSG00000113615			Sec24a (MGI:1924621)			
chr5	134738479	134752159	5q23	5q31.1		601118	CAMLG	Calcium-modulating cyclophilin ligand	CAMLG	819	ENSG00000164615			Caml (MGI:104728)			
chr5	134758733	134831137	5q31.1	5q31.1		617848	"DDX46, PRP5, KIAA0801"	DEAD box helicase 46	DDX46	9879	ENSG00000145833			Ddx46 (MGI:1920895)			
chr5	134873769	134901632	5q31.1	5q31.1		617778	"TXNDC15, C5orf14, BUG"	Thioredoxin domain-containing protein 15	TXNDC15	79770	ENSG00000113621			Txndc15 (MGI:1916922)			
chr5	134905119	134962645	5q31.2	5q31.1		609836	"PCBD2, DCOH2, DCOHM"	Pterin-4-alpha-carbinolamine dehydratase 2	PCBD2	84105	ENSG00000132570			Pcbd2 (MGI:1919812)			
chr5	134967905	135011706	5q31.1	5q31.1		609120	"CATSPER3, CACRC"	"Cation channel, sperm-associated, 3"	CATSPER3	347732	ENSG00000152705			Catsper3 (MGI:1924106)			
chr5	135027733	135034273	5q31	5q31.1		602149	"PITX1, PTX1, BFT, POTX, CCF, LBNBG"	Paired-like homeodomain transcription factor-1	PITX1	5307	ENSG00000069011		"Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly, 119800 (3), Autosomal dominant; Liebenberg syndrome, 186550 (4), Autosomal dominant"	Pitx1 (MGI:107374)			
chr5	135334380	135401997	5q31.3-q32	5q31.1		610054	"H2AFY, MH2A1"	"H2A histone family, member Y"	H2AFY	9555	ENSG00000113648			H2afy (MGI:1349392)			
chr5	135444213	135447347	5q31.1	5q31.1		609710	"C5orf20, DCNP1"	Dendritic cell nuclear protein 1	DCANP1	140947	ENSG00000251380						
chr5	135448867	135452398	5q31.2	5q31.1		612663	TIFAB	"TRAF-interacting protein with forkhead-associated domain, family member B"	TIFAB	497189	ENSG00000255833			Tifab (MGI:2385852)			
chr5	135534281	135535948	5q23-q31	5q31.1		601726	"NEUROG1, NEUROD3"	Neurogenin 1	NEUROG1	4762	ENSG00000181965			Neurog1 (MGI:107754)			
chr5	135570678	135579278	5q31	5q31.1		604186	"CXCL14, SCYB14, BRAK"	"Chemokine, C-X-C motif, ligand 14"	CXCL14	9547	ENSG00000145824			Cxcl14 (MGI:1888514)			
chr5	135579164	135888636	5q31.1	5q31.1		616150	SLC25A48	"Solute carrier family 25, member 48"	SLC25A48	153328	ENSG00000145832						
chr5	135892245	135895826	5q31.1	5q31.1		146931	IL9	Interleukin-9	IL9	3578	ENSG00000145839			Il9 (MGI:96563)			
chr5	135930296	135941995	5q31.1	5q31.1		609087	"FBXL21, FBL21, FBXL3B, FBL3B"	F-box and leucine-rich repeat protein 21	FBXL21	26223				Fbxl21 (MGI:2442921)			
chr5	135946910	135955033	5q31.1-q32	5q31.1		602882	LECT2	Leukocyte cell-derived chemotaxin 2	LECT2	3950	ENSG00000145826			Lect2 (MGI:1278342)			
chr5	136028894	136063817	5q31	5q31.1		601692	"TGFBI, CSD2, CDGG1, CSD, BIGH3, CDG2, EBMD"	"Transforming growth factor, beta-induced, 68kD"	TGFBI	7045	ENSG00000120708		"Corneal dystrophy, Avellino type, 607541 (3), Autosomal dominant; Corneal dystrophy, Groenouw type I, 121900 (3), Autosomal dominant; Corneal dystrophy, Reis-Bucklers type, 608470 (3); Corneal dystrophy, Thiel-Behnke type, 602082 (3), Autosomal dominant; Corneal dystrophy, epithelial basement membrane, 121820 (3), Autosomal dominant; Corneal dystrophy, lattice type I, 122200 (3), Autosomal dominant; Corneal dystrophy, lattice type IIIA, 608471 (3), Autosomal dominant"	Tgfbi (MGI:99959)			
chr5	136080490	136080597	5q31	5q31.1		614938	"VTRNA2-1, NC886, CBL3, VTRNA2"	Vault RNA 2-1	VTRNA2-1	100126299							
chr5	136132844	136182733	5q31	5q31.1		603110	"MADH5, SMAD5"	"Mothers against decapentaplegic, Drosophila, homolog of, 5"	SMAD5	4090	ENSG00000113658			Smad5 (MGI:1328787)			
chr5	136975297	137499328	5q31	5q31.2		602264	SPOCK	Testican	SPOCK1	6695	ENSG00000152377	previously mapped to chr.21		Spock1 (MGI:105371)			
chr5	137617499	137736089	5q31	5q31.2		605775	"KLHL3, PHA2D"	Kelch-like 3	KLHL3	26249	ENSG00000146021		"Pseudohypoaldosteronism, type IID, 614495 (3), Autosomal recessive, Autosomal dominant"	Klhl3 (MGI:2445185)			
chr5	137751383	137754349	5q31	5q31.2		609409	HNRPA0	Heterogeneous nuclear ribonucleoprotein A0	HNRNPA0	10949	ENSG00000177733			Hnrnpa0 (MGI:1924384)			
chr5	137801192	137810750	5q31	5q31.2		601770	"NPY6R, PP2"	Neuropeptide Y receptor Y6	NPY6R	4888		?nonfunctional pseudogene					
chr5	137867281	137887850	5q31	5q31.2		604103	"MYOT, TTOD, MFM3"	Myotilin (titin immunoglobulin domain protein)	MYOT	9499	ENSG00000120729		"Muscular dystrophy, limb-girdle, type 1A, 159000 (3), Autosomal dominant; Myopathy, myofibrillar, 3, 609200 (3), Autosomal dominant; Myopathy, spheroid body, 182920 (3), Autosomal dominant"	Myot (MGI:1889800)			
chr5	137889410	137942746	5q31	5q31.2		604669	PKD2L2	Polycystin 2-like 2	PKD2L2	27039	ENSG00000078795			Pkd2l2 (MGI:1858231)			
chr5	137937908	138051960	5q31.2	5q31.2		609371	"FAM13B, C5orf5"	"Family with sequence similarity 13, member B"	FAM13B	51306	ENSG00000031003			Fam13b (MGI:2447834)			
chr5	138077366	138092899	5q31.2	5q31.2		606360	WNT8A	"Wingless-type MMTV integration site family, member 8A"	WNT8A	7478	ENSG00000061492			Wnt8a (MGI:107924)			
chr5	138115171	138139470	5q23-q31	5q31.2		603575	"NME5, NM23H5"	"Nonmetastatic cells 5, protein expressed in (nonmetastatic protein 23, homolog 5)"	NME5	8382	ENSG00000112981			Nme5 (MGI:1922783)			
chr5	138139765	138178668	5q31.2	5q31.2		602848	"BRD8, SMAP"	Bromodomain-containing protein 8	BRD8	10902	ENSG00000112983			Brd8 (MGI:1925906)			
chr5	138178727	138187714	5q31	5q31.2		605664	"KIF20A, RAB6KIFL"	Kinesin family member 20A	KIF20A	10112	ENSG00000112984			Kif20a (MGI:1201682)			
chr5	138187647	138213342	5q31.1	5q31.2		603462	"CDC23, APC8"	Cell division cycle 23 (anaphase-promoting complex 8)	CDC23	8697	ENSG00000094880			Cdc23 (MGI:1098815)			
chr5	138252379	138274563	5q31	5q31.2		605710	GFRA3	GDNF family receptor alpha-3	GFRA3	2676	ENSG00000146013			Gfra3 (MGI:1201403)			
chr5	138285264	138338354	5q31	5q31.2		157680	CDC25C	Cell division cycle 25C	CDC25C	995	ENSG00000158402			Cdc25c (MGI:88350)			
chr5	138337534	138349728	5q31.2	5q31.2		609372	"FAM53C, C5orf6"	"Family with sequence similarity 53, member C"	FAM53C	51307	ENSG00000120709			Fam53c (MGI:1913556)			
chr5	138352595	138437026	5q31	5q31.2		609373	"KDM3B, C5orf7, KIAA1082, JMJD1B"	Lysine-specific demethylase 3B	KDM3B	51780	ENSG00000120733			Kdm3b (MGI:1923356)			
chr5	138439000	138446968	5q31	5q31.2		609347	"REEP2, C5orf19, SPG72"	Receptor expression-enhancing protein 2	REEP2	51308	ENSG00000132563	mutation identified in 1 family each SPG72 AR and AD	"?Spastic paraplegia 72, autosomal dominant, 615625 (3), Autosomal recessive, Autosomal dominant; ?Spastic paraplegia 72, autosomal recessive, 615625 (3), Autosomal recessive, Autosomal dominant"	Reep2 (MGI:2385070)			
chr5	138465491	138469314	5q31.1	5q31.2		128990	EGR1	Early growth response-1	EGR1	1958	ENSG00000120738			Egr1 (MGI:95295)			
chr5	138506092	138543299	5q31.1	5q31.2		600285	"ETF1, RF1, ERF1"	Eukaryotic translation termination factor-1	ETF1	2107	ENSG00000120705			Etf1 (MGI:2385071)			
chr5	138554881	138575628	5q31.2	5q31.2		600548	"HSPA9, HSPA9B, MOT2, GRP75, EVPLS, SIDBA4"	Heat-shock 70kD protein-9 (mortalin)	HSPA9	3313	ENSG00000113013		"Anemia, sideroblastic, 4, 182170 (3), Autosomal dominant; Even-plus syndrome, 616854 (3), Autosomal recessive"	Hspa9 (MGI:96245)			
chr5	138753385	138935033	5q31	5q31.2		116805	"CTNNA1, MDPT2"	"Catenin (cadherin-associated protein), alpha 1, 102kD"	CTNNA1	1495	ENSG00000044115		"Macular dystrophy, patterned, 2, 608970 (3), Autosomal dominant"	Ctnna1 (MGI:88274)			
chr5	138869389	138875367	5q31.2	5q31.2		610868	"LRRTM2, KIAA0416"	Leucine-rich repeat transmembrane protein 2	LRRTM2	26045	ENSG00000146006			Lrrtm2 (MGI:2389174)			
chr5	138946719	139198375	5q31	5q31.2		608005	"SIL1, BAP, MSS"	"Sil1, S. cerevisiae, homolog of"	SIL1	64374	ENSG00000120725		"Marinesco-Sjogren syndrome, 248800 (3), Autosomal recessive"	Sil1 (MGI:1932040)			
chr5	139273751	139331676	5q31.2	5q31.2		164015	"MATR3, MPD2, ALS21"	Matrin 3	MATR3	9782	ENSG00000015479		"Amyotrophic lateral sclerosis 21, 606070 (3), Autosomal dominant"	Matr3 (MGI:1298379)			
chr5	139341831	139369719	5q31.2	5q31.2		605604	"PAIP2, PAIP2A"	Polyadenylate-binding protein-interacting protein 2	PAIP2	51247	ENSG00000120727			Paip2 (MGI:1915119)			
chr5	139367195	139384552	5q31.2-q31.3	5q31.2		603790	"SLC23A1, SVCT1"	"Solute carrier family 23 (nucleobase transporter), member 1 (sodium-dependent vitamin C transporter 1)"	SLC23A1	9963	ENSG00000170482	opposite orientation to MATR3		Slc23a1 (MGI:1341903)			
chr5	139387567	139389915	5q31.2	5q31.2		609447	"MZB1, PACAP, MGC29506"	Marginal zone B and B1 cell-specific protein	MZB1	51237	ENSG00000170476			Mzb1 (MGI:1917066)			
chr5	139448553	139462742	5q31	5q31.2		615736	"ECSCR, ECSM2, ARIA"	Endothelial cell surface-expressed chemotaxis and apoptosis regulator	ECSCR	641700	ENSG00000249751			Ecscr (MGI:1915795)			
chr5	139475527	139482789	5q31.2	5q31.2		612374	"TMEM173, STING, MPYS, SAVI"	Transmembrane protein 173	TMEM173	340061	ENSG00000184584		"STING-associated vasculopathy, infantile-onset, 615934 (3), Autosomal dominant"	Tmem173 (MGI:1919762)			
chr5	139561165	139628433	5q31.2	5q31.2		602962	"UBE2D2, UBCH5B, UBC4"	Ubiquitin-conjugating enzyme E2D 2	UBE2D2	7322	ENSG00000131508			Ube2d2a (MGI:1930715)			
chr5	139647298	139683884	5q31.3	5q31.2		612752	CXXC5	CXXC finger protein 5	CXXC5	51523	ENSG00000171604			Cxxc5 (MGI:1914643)			
chr5	139846778	140043674	5q23-q33	5q31.2		603818	NRG2	Neuregulin 2	NRG2	9542	ENSG00000158458			Nrg2 (MGI:1098246)			
chr5	140100000	150400000	5q31.3-q32			601101	"HHT3, ORW3"	"Hereditary hemorrhagic telangiectasia, type 3"		780903			"Telangiectasia, hereditary hemorrhagic, type 3, 601101 (2)"				
chr5	140114122	140119415	5q31	5q31.3		600473	"PURA, PUR1, MRD31"	Purine-rich element binding protein A	PURA	5813	ENSG00000185129		"Mental retardation, autosomal dominant 31, 616158 (3), Autosomal dominant"	Pura (MGI:103079)			
chr5	140245049	140303103	5q31	5q31.3		604897	PFDN1	Prefoldin 1	PFDN1	5201	ENSG00000113068			Pfdn1 (MGI:1914449)			
chr5	140332842	140346602	5q23	5q31.3		126150	"HBEGF, DTR, DTSF, HEGFL"	Heparin-binding EGF-like growth factor (diphtheria toxin receptor)	HBEGF	1839	ENSG00000113070		"{Diphtheria, susceptibility to} (1)"	Hbegf (MGI:96070)			
chr5	140401813	140539855	5q31.3	5q31.3		610500	"ANKHD1, MASK, KIAA1085, VBARP"	Ankyrin repeat and KH domain-containing protein 1	ANKHD1	54882	ENSG00000131503			Ankhd1 (MGI:1921733)			
chr5	140550066	140558092	5q31.3	5q31.3		603819	SRA1	Steroid receptor RNA activator 1	SRA1	10011	ENSG00000213523			Sra1 (MGI:1344414)			
chr5	140558267	140564603	5q31	5q31.3		602711	"APBB3, FE65L2"	"Amyloid beta (A4) precursor protein-binding, family B, member 3"	APBB3	10307	ENSG00000113108			Apbb3 (MGI:108404)			
chr5	140631727	140633700	5q31.1	5q31.3		158120	CD14	CD14 antigen	CD14	929	ENSG00000170458			Cd14 (MGI:88318)			
chr5	140645362	140647784	5q31.2	5q31.3		602137	NDUFA2	"NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 (8kD, B8)"	NDUFA2	4695	ENSG00000131495		"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufa2 (MGI:1343103)			
chr5	140647798	140662479	5q31.3	5q31.3		600549	"IK, RED"	"IK cytokine, downregulator of HLA II"	IK	3550	ENSG00000113141			Ik (MGI:1345142)			
chr5	140670795	140673585	5q31.3	5q31.3		609385	DND1	"Dead end, zebrafish, homolog of, 1"	DND1	373863	ENSG00000256453			Dnd1 (MGI:2447763)			
chr5	140673903	140691726	5q31.3	5q31.3		142810	"HARS, USH3B, CMT2W"	Histidyl-tRNA synthetase	HARS	3035	ENSG00000170445		"Charcot-Marie-Tooth disease, axonal, type 2W, 616625 (3), Autosomal dominant; Usher syndrome type 3B, 614504 (3), Autosomal recessive"	Hars (MGI:108087)			
chr5	140691425	140699317	5q31.3	5q31.3		600783	"HARS2, HARSL, HARSR, HO3, PRLTS2"	Histidyl-tRNA synthetase 2	HARS2	23438	ENSG00000112855	mutation identified in 1 PRLTS2 family	"?Perrault syndrome 2, 614926 (3), Autosomal recessive"	Hars2 (MGI:1918041)			
chr5	140711275	140711372	5q31	5q31.3		612695	"VTRNA1-1, HVG1, VAULTRC1"	Vault RNA 1-1	VTRNA1-1	56664							
chr5	140718925	140719012	5q31	5q31.3		612696	"VTRNA1-2, HVG2, VAULTRC2"	Vault RNA 1-2	VTRNA1-2	56663							
chr5	140726158	140726245	5q31	5q31.3		612697	"VTRNA1-3, HVG3, VAULTRC3"	Vault RNA 1-3	VTRNA1-3	56662							
chr5	140786135	141012343	5q31	5q31.3		606307	PCDHA1	Protocadherin-alpha 1	PCDHA1	56147	ENSG00000204970			Pcdha1 (MGI:2150982)			
chr5	140794858	141012343	5q31	5q31.3		606308	PCDHA2	Protocadherin-alpha 2	PCDHA2	56146	ENSG00000204969			Pcdha2 (MGI:2681880)			
chr5	140801197	141012343	5q31	5q31.3		606309	PCDHA3	Protocadherin-alpha 3	PCDHA3	56145	ENSG00000255408			Pcdha3 (MGI:2447313)			
chr5	140807073	141012343	5q31	5q31.3		606310	PCDHA4	Protocadherin-alpha 4	PCDHA4	56144	ENSG00000204967			Pcdha4 (MGI:1298406)			
chr5	140821775	141012343	5q31	5q31.3		606311	PCDHA5	Protocadherin-alpha 5	PCDHA5	56143	ENSG00000204965			Pcdha5 (MGI:1298371)			
chr5	140827921	141012343	5q31	5q31.3		606312	PCDHA6	Protocadherin-alpha 6	PCDHA6	56142	ENSG00000081842			Pcdha6 (MGI:1298367)			
chr5	140834383	141012343	5q31	5q31.3		606313	PCDHA7	Protocadherin-alpha 7	PCDHA7	56141	ENSG00000204963			Pcdha7 (MGI:1298369)			
chr5	140841321	141012343	5q31	5q31.3		606314	PCDHA8	Protocadherin-alpha 8	PCDHA8	56140	ENSG00000204962						
chr5	140847771	141012343	5q31	5q31.3		606315	PCDHA9	Protocadherin-alpha 9	PCDHA9	9752	ENSG00000204961			Pcdha8 (MGI:2681879)			
chr5	140855882	141012343	5q31	5q31.3		606316	PCDHA10	Protocadherin-alpha 10	PCDHA10	56139	ENSG00000250120			Pcdha9 (MGI:2447322)			
chr5	140867512	141012343	5q31	5q31.3		606317	PCDHA11	Protocadherin-alpha 11	PCDHA11	56138	ENSG00000249158			Pcdha11 (MGI:1298372)			
chr5	140875301	141012343	5q31	5q31.3		606318	PCDHA12	Protocadherin-alpha 12	PCDHA12	56137	ENSG00000251664			Pcdha10 (MGI:1298408)			
chr5	140882268	141012343	5q31	5q31.3		606319	PCDHA13	Protocadherin-alpha 13	PCDHA13	56136	ENSG00000239389			Pcdha12 (MGI:1298370)			
chr5	140926716	141012343	5q31	5q31.3		606320	PCDHAC1	"Protocadherin-alpha, subfamily C, member 1"	PCDHAC1	56135	ENSG00000248383			Pcdhac1 (MGI:1891442)			
chr5	140966161	141012343	5q31	5q31.3		606321	PCDHAC2	"Protocadherin-alpha, subfamily C, member 2"	PCDHAC2	56134	ENSG00000243232			Pcdhac2 (MGI:1891443)			
chr5	141051375	141053961	5q31	5q31.3		606327	PCDHB1	Protocadherin-beta 1	PCDHB1	29930	ENSG00000171815			Pcdhb1 (MGI:2136730)			
chr5	141094606	141097379	5q31	5q31.3		606328	PCDHB2	Protocadherin-beta 2	PCDHB2	56133	ENSG00000112852			Pcdhb2 (MGI:2136735)			
chr5	141100241	141103826	5q31	5q31.3		606329	PCDHB3	Protocadherin-beta 3	PCDHB3	56132	ENSG00000113205			Pcdhb3 (MGI:2136737)			
chr5	141121749	141125622	5q31	5q31.3		606330	PCDHB4	Protocadherin-beta 4	PCDHB4	56131	ENSG00000081818			Pcdhb5 (MGI:2136739)			
chr5	141135205	141138126	5q31	5q31.3		606331	PCDHB5	Protocadherin-beta 5	PCDHB5	26167	ENSG00000113209			Pcdhb10 (MGI:2136745)			
chr5	141150021	141153286	5q31	5q31.3		606332	PCDHB6	Protocadherin-beta 6	PCDHB6	56130	ENSG00000113211			Pcdhb13 (MGI:2136748)			
chr5	141172620	141176375	5q31	5q31.3		606333	PCDHB7	Protocadherin-beta 7	PCDHB7	56129	ENSG00000113212			Pcdhb15 (MGI:2136750)			
chr5	141177789	141180499	5q31	5q31.3		606334	PCDHB8	Protocadherin-beta 8	PCDHB8	56128	ENSG00000120322			Pcdhb16 (MGI:2136752)			
chr5	141181689	141186220	5q31	5q31.3		606345	PCDHB16	Protocadherin-beta 16	PCDHB16	57717	ENSG00000272674			Pcdhb17 (MGI:2136754)			
chr5	141187126	141191537	5q31	5q31.3		606335	PCDHB9	Protocadherin-beta 9	PCDHB9	56127	ENSG00000177839						
chr5	141192378	141195639	5q31	5q31.3		606336	PCHB10	Protocadherin-beta 10	PCDHB10	56126	ENSG00000120324						
chr5	141199774	141203044	5q31	5q31.3		606337	PCDHB11	Protocadherin-beta 11	PCDHB11	56125	ENSG00000197479			Pcdhb21 (MGI:2136759)			
chr5	141208718	141212125	5q31	5q31.3		606338	PCDHB12	Protocadherin-beta 12	PCDHB12	56124	ENSG00000120328			Pcdhb19 (MGI:2136757)			
chr5	141213918	141217420	5q31	5q31.3		606339	PCDHB13	Protocadherin-beta 13	PCDHB13	56123	ENSG00000187372						
chr5	141222325	141226287	5q31	5q31.3		606340	PCDHB14	Protocadherin-beta 14	PCDHB14	56122	ENSG00000120327			Pcdhb20 (MGI:2136758)			
chr5	141245348	141248233	5q31	5q31.3		606341	PCDHB15	Protocadherin-beta 15	PCDHB15	56121	ENSG00000113248			Pcdhb22 (MGI:2136760)			
chr5	141302628	141304062	5q31	5q31.3		608157	"SLC25A2, ORNT2"	"Solute carrier family 25 (mitochondrial carrier, ornithine transporter), member 2"	SLC25A2	83884	ENSG00000120329						
chr5	141318489	141320783	5q31	5q31.3		600573	"TAF7, TAF2F, TAFII55"	"TAF7 RNA polymerase II, TATA box-binding protein-associated factor, 55kD"	TAF7	6879	ENSG00000178913			Taf7 (MGI:1346348)			
chr5	141330684	141512978	5q31	5q31.3		606288	PCDHGA1	"Protocadherin-gamma, subfamily A, member 1"	PCDHGA1	56114	ENSG00000204956			Pcdhga1 (MGI:1935212)			
chr5	141338759	141512978	5q31	5q31.3		606289	PCDHGA2	"Protocadherin-gamma, subfamily A, member 2"	PCDHGA2	56113	ENSG00000081853			Pcdhga2 (MGI:1935214)			
chr5	141344033	141512978	5q31	5q31.3		606290	PCDHGA3	"Protocadherin-gamma, subfamily A, member 3"	PCDHGA3	56112	ENSG00000254245			Pcdhga3 (MGI:1935215)			
chr5	141350260	141512978	5q31	5q31.3		606299	PCDHGB1	"Protocadherin-gamma, subfamily B, member 1"	PCDHGB1	56104	ENSG00000254221			Pcdhgb1 (MGI:1935169)			
chr5	141355024	141512978	5q31	5q31.3		606291	PCDHGA4	"Protocadherin-gamma, subfamily A, member 4"	PCDHGA4	56111	ENSG00000262576			Pcdhga4 (MGI:1935216)			
chr5	141360135	141512978	5q31	5q31.3		606300	PCDHGB2	"Protocadherin-gamma, subfamily B, member 2"	PCDHGB2	56103	ENSG00000253910			Pcdhgb2 (MGI:1935170)			
chr5	141364330	141512978	5q31	5q31.3		606292	PCDHGA5	"Protocadherin-gamma, subfamily A, member 5"	PCDHGA5	56110	ENSG00000253485			Pcdhga5 (MGI:1935217)			
chr5	141370263	141512978	5q31	5q31.3		606301	PCDHGB3	"Protocadherin-gamma, subfamily B, member 3"	PCDHGB3	56102	ENSG00000262209			Pcdhgb8 (MGI:1935200)			
chr5	141374083	141512978	5q31	5q31.3		606293	PCDHGA6	"Protocadherin-gamma, subfamily A, member 6"	PCDHGA6	56109	ENSG00000253731			Pcdhga6 (MGI:1935218)			
chr5	141382738	141512978	5q31	5q31.3		606294	PCDHGA7	"Protocadherin-gamma, subfamily A, member 7"	PCDHGA7	56108	ENSG00000253537			Pcdhga7 (MGI:1935219)			
chr5	141387884	141512978	5q31	5q31.3		603058	PCDHGB4	"Protocadherin-gamma, subfamily B, member 4"	PCDHGB4	8641	ENSG00000253953			Pcdhgb4 (MGI:1935173)			
chr5	141391915	141512978	5q31	5q31.3		606295	PCDHGA8	"Protocadherin-gamma, subfamily A, member 8"	PCDHGA8	9708	ENSG00000253767			Pcdhga8 (MGI:1935221)			
chr5	141398127	141512978	5q31	5q31.3		606302	PCDHGB5	"Protocadherin-gamma, subfamily B, member 5"	PCDHGB5	56101	ENSG00000276547			Pcdhgb5 (MGI:1935196)			
chr5	141402952	141512978	5q31	5q31.3		606296	PCDHGA9	"Protocadherin-gamma, subfamily A, member 9"	PCDHGA9	56107	ENSG00000261934			Pcdhga9 (MGI:1935226)			
chr5	141408202	141512978	5q31	5q31.3		606303	PCDHGB6	"Protocadherin-gamma, subfamily B, member 6"	PCDHGB6	56100	ENSG00000253305			Pcdhgb6 (MGI:1935197)			
chr5	141413175	141512978	5q31	5q31.3		606297	PCDHGA10	"Protocadherin-gamma, subfamily A, member 10"	PCDHGA10	56106	ENSG00000253846			Pcdhga10 (MGI:1935227)			
chr5	141417646	141512980	5q31	5q31.3		606304	PCDHGB7	"Protocadherin-gamma, subfamily B, member 7"	PCDHGB7	56099	ENSG00000254122			Pcdhgb7 (MGI:1935199)			
chr5	141420969	141512978	5q31	5q31.3		606298	PCDHGA11	"Protocadherin-gamma, subfamily A, member 11"	PCDHGA11	56105	ENSG00000253873			Pcdhga11 (MGI:1935228)			
chr5	141430590	141512978	5q31	5q31.3		603059	PCDHGA12	"Protocadherin-gamma, subfamily A, member 12"	PCDHGA12	26025	ENSG00000253159			Pcdhga12 (MGI:1935229)			
chr5	141476001	141512976	5q31	5q31.3		603627	PCDHGC3	"Protocadherin-gamma, subfamily C, member 3"	PCDHGC3	5098	ENSG00000240184			Pcdhgc3 (MGI:1935201)			
chr5	141485173	141512978	5q31	5q31.3		606305	PCDHGC4	"Protocadherin-gamma, subfamily C, member 4"	PCDHGC4	56098	ENSG00000242419			Pcdhgc4 (MGI:1935203)			
chr5	141489240	141512978	5q31	5q31.3		606306	PCDHGC5	"Protocadherin-gamma, subfamily C, member 5"	PCDHGC5	56097	ENSG00000240764			Pcdhgc5 (MGI:1935205)			
chr5	141515015	141619054	5q31	5q31.3		602121	"DIAPH1, DFNA1, LFHL1, SCBMS"	"Diaphanous, Drosophila, homolog of, 1"	DIAPH1	1729	ENSG00000131504		"Deafness, autosomal dominant 1, 124900 (3), Autosomal dominant; Seizures, cortical blindness, microcephaly syndrome, 616632 (3), Autosomal recessive"	Diaph1 (MGI:1194490)			
chr5	141620875	141636855	5q31	5q31.3		605166	HDAC3	Histone deacetylase 3	HDAC3	8841	ENSG00000171720			Hdac3 (MGI:1343091)			
chr5	141636949	141641076	5q31.3	5q31.3		611213	RELL2	Relt-like 2	RELL2	285613	ENSG00000164620			Rell2 (MGI:1918044)			
chr5	141639301	141651442	5q31.3	5q31.3		617555	"FCHSD1, NWK2"	FCH and double SH3 domains protein 1	FCHSD1	89848	ENSG00000197948			Fchsd1 (MGI:2441771)			
chr5	141653400	141682232	5q31.3	5q31.3		606647	"ARAP3, CENTD3"	"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3"	ARAP3	64411	ENSG00000120318			Arap3 (MGI:2147274)			
chr5	141850392	141878409	5q32-q33	5q31.3		603626	"PCDH1, PC42"	Protocadherin 1 (cadherin-like 1)	PCDH1	5097	ENSG00000156453			Pcdh1 (MGI:104692)			
chr5	141923819	141952030	5q31.3	5q31.3		615741	"KIAA0141, DELE"	KIAA0141 gene	DELE1	9812	ENSG00000081791			0610009O20Rik (MGI:1914089)			
chr5	141943584	141959061	5q31	5q31.3		605622	"PCDH12, VECAD2, PCDH12"	"Protocadherin 12 (cadherin, vascular endothelial, 2)"	PCDH12	51294	ENSG00000113555		"Microcephaly, seizures, spasticity, and brain calcification, 605622 (3)"	Pcdh12 (MGI:1855700)			
chr5	141966806	141990290	5q23.3-q31.1	5q31.3		605675	"RNF14, ARA54"	RING finger protein-14	RNF14	9604	ENSG00000013561			Rnf14 (MGI:1929668)			
chr5	142000668	142013054	5q31	5q31.3		601798	"GNPDA1, GNP1, GNPI, KIAA0060"	Glucosamine 6-phosphate deaminase 1	GNPDA1	10007	ENSG00000113552			Gnpda1 (MGI:1347054)			
chr5	142108758	142154442	5q31.3	5q31.3		612050	"NDFIP1, N4WBP5"	NEDD4 family-interacting protein 1	NDFIP1	80762	ENSG00000131507			Ndfip1 (MGI:1929601)			
chr5	142310426	142325054	5q31.3	5q31.3		607984	"SPRY4, HH17"	"Sprouty, Drosophila, homolog of"	SPRY4	81848	ENSG00000187678		"Hypogonadotropic hypogonadism 17 with or without anosmia, 615266 (3), Autosomal dominant"	Spry4 (MGI:1345144)			
chr5	142317619	142318321	5q31.3	5q31.3		617617	SPRY4IT1	"SPRY4 intronic transcript 1, noncoding"	SPRY4-IT1	100642175		in intron 2 of SPRY4					
chr5	142592177	142698069	5q31	5q31.3		131220	"FGF1, FGFA"	Fibroblast growth factor-1 (acidic)	FGF1	2246	ENSG00000113578			Fgf1 (MGI:95515)			
chr5	142770369	143229010	5q31	5q31.3		605370	"ARHGAP26, GRAF"	RHO GTPase-activating protein 26	ARHGAP26	23092	ENSG00000145819		"Leukemia, juvenile myelomonocytic, somatic, 607785 (3)"	Arhgap26 (MGI:1918552)			
chr5	143277930	143435511	5q31	5q31.3		138040	"NR3C1, GCR, GRL, GCRST"	"Nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)"	NR3C1	2908	ENSG00000113580		"Glucocorticoid resistance, 615962 (3), Autosomal dominant"	Nr3c1 (MGI:95824)			
chr5	143812160	143820718	5q32	5q31.3		609961	HLA-HB1	Minor histocompatibility antigen HB-1	HMHB1	57824	ENSG00000158497						
chr5	144158158	144170713	5q32	5q31.3		611483	"YIPF5, SMAP5, YIP1A"	"Yip1 domain family, member 5"	YIPF5	81555	ENSG00000145817			Yipf5 (MGI:1914430)			
chr5	144170722	144485685	5q31.3	5q31.3		613423	"KCTD16, KIAA1317"	Potassium channel tetramerization domain-containing 16	KCTD16	57528	ENSG00000183775			Kctd16 (MGI:1914659)			
chr5	145858537	145931672	5q32	5q32		615762	"GRXCR2, DFNB101"	"Glutaredoxin, cysteine-rich, 2"	GRXCR2	643226	ENSG00000204928	mutation identified in 1 DFNB101 family	"?Deafness, autosomal recessive 101, 615837 (3), Autosomal recessive"	Grxcr2 (MGI:2685697)			
chr5	145936562	146081772	5q32	5q32		613377	"SH3RF2, HEPP1"	SH3 domain-containing RING finger protein 2	SH3RF2	153769	ENSG00000156463			Sh3rf2 (MGI:2444628)			
chr5	146113025	146182786	5q32	5q32		151350	"LARS, LFIS, ILFS1"	Leucyl-tRNA synthetase	LARS	51520	ENSG00000133706	mutation identified in 1 family	"?Infantile liver failure syndrome 1, 615438 (3), Autosomal recessive"	Lars (MGI:1913808)			
chr5	146339023	146340519	5q31	5q32		602460	"POU4F3, BRN3C"	"POU domain, class 4, transcription factor-3"	POU4F3	5459	ENSG00000091010		"Deafness, autosomal dominant 15, 602459 (3), Autosomal dominant"	Pou4f3 (MGI:102523)			
chr5	146447309	146511507	5q31	5q32		605409	"TCERG1, TAF2S, CA150"	Transcription elongation regulator 1 (transcription factor CA150)	TCERG1	10915	ENSG00000113649			Tcerg1 (MGI:1926421)			
chr5	146589503	147081519	5q31-q33	5q32		604325	PPP2R2B	"Protein phosphatase 2, regulatory subunit B, beta"	PPP2R2B	5521	ENSG00000156475		"Spinocerebellar ataxia 12, 604326 (3), Autosomal dominant"	Ppp2r2b (MGI:1920180)			
chr5	147390807	147510055	5q32	5q32		601168	"DPYSL3, ULIP, DRP3"	Dihydropyrimidinase-like 3	DPYSL3	1809	ENSG00000113657			Dpysl3 (MGI:1349762)			
chr5	147585438	147782847	5q32	5q32		611197	"JAKMIP2, JAMIP2, NECC1, KIAA0555"	Janus kinase and microtubule-interacting protein 2	JAKMIP2	9832	ENSG00000176049			Jakmip2 (MGI:1923467)			
chr5	147824579	147839230	5q32	5q32		167790	"SPINK1, PSTI, PCTT, TATI, TCP"	"Serine protease inhibitor, Kazal type I (pancreatic secretory trypsin inhibitor)"	SPINK1	6690	ENSG00000164266		"{Fibrocalculous pancreatic diabetes, susceptibility to}, 608189 (3), Autosomal recessive, Autosomal dominant; Pancreatitis, hereditary, 167800 (3), Autosomal dominant; Tropical calcific pancreatitis, 608189 (3), Autosomal recessive, Autosomal dominant"	Spink1 (MGI:106202)			
chr5	147878710	147882192	5q31-q34	5q32		606531	"SCGB3A2, UGRP1"	"Secretoglobin, family 3A, member 2 (uteroglobin-related protein 1)"	SCGB3A2	117156	ENSG00000164265		"{Asthma, susceptibility to}, 600807 (3), Autosomal dominant"	Scgb3a2 (MGI:2153470)			
chr5	148063971	148137361	5q32	5q32		605010	"SPINK5, LEKTI"	"Serine protease inhibitor, Kazal type, 5"	SPINK5	11005	ENSG00000133710		"Netherton syndrome, 256500 (3), Autosomal recessive"	Spink5 (MGI:1919682)			
chr5	148202793	148215136	5q32	5q32		615868	SPINK6	"Serine peptidase inhibitor, KAZAL-type, 6"	SPINK6	404203	ENSG00000178172						
chr5	148268859	148286209	5q32	5q32		615205	SPINK13	"Serine protease inhibitor, Kazal-type, 13"	SPINK13	153218	ENSG00000214510			Spink13 (MGI:3642511)			
chr5	148312426	148315918	5q32	5q32		617288	"SPINK7, ECRG2"	"Serine peptidase inhibitor, Kazal-type, 7"	SPINK7	84651	ENSG00000145879			Spink7 (MGI:3644691)			
chr5	148323218	148341973	5q33.1	5q32		613511	"SPINK9, LEKTI2"	"Serine protease inhibitor, Kazal-type, 9"	SPINK9	643394	ENSG00000204909						
chr5	148383934	148442835	5q33.1	5q32		608533	"FBXO38, FBX38, MOKA, HMN2D"	F-box only protein 38	FBXO38	81545	ENSG00000145868		"Neuronopathy, distal hereditary motor, type IID, 615575 (3), Autosomal dominant"				
chr5	148451031	148654526	5q31-q33	5q32		602164	HTR4	5-hydroxytryptamine (serotonin) receptor-4	HTR4	3360	ENSG00000164270			Htr4 (MGI:109246)			
chr5	148826592	148828633	5q32-q34	5q32		109690	ADRB2	"Adrenergic, beta-2-, receptor, surface"	ADRB2	154			"{Asthma, nocturnal, susceptibility to}, 600807 (3), Autosomal dominant; Beta-2-adrenoreceptor agonist, reduced response to (3); {Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Adrb2 (MGI:87938)			
chr5	148982149	149063173	5q32	5q32		608206	"SH3TC2, KIAA1985, MNMN"	SH3 domain and tetratricopeptide repeat domain 2	SH3TC2	79628	ENSG00000169247		"Charcot-Marie-Tooth disease, type 4C, 601596 (3), Autosomal recessive; Mononeuropathy of the median nerve, mild, 613353 (3), Autosomal dominant"	Sh3tc2 (MGI:2444417)			
chr5	149141446	149260438	5q32	5q32		611305	"ABLIM3, KIAA0843"	"Actin-binding LIM protein family, member 3"	ABLIM3	22885	ENSG00000173210			Ablim3 (MGI:2442582)			
chr5	149271837	149343636	5q33.1	5q32		614410	AFAP1L1	Actin filament-associated protein 1-like 1	AFAP1L1	134265	ENSG00000157510			Afap1l1 (MGI:2147199)			
chr5	149374266	149404201	5q32-q34	5q32		604627	IL17B	Interleukin 17B	IL17B	27190	ENSG00000127743			Il17b (MGI:1928397)			
chr5	149428917	149429022	5q33.1	5q32		612117	"MIR143, MIRN143"	Micro RNA 143	MIR143	406935							
chr5	149430645	149430732	5q33.1	5q32		611795	"MIR145, MIRN145"	Micro RNA 145	MIR145	406937							
chr5	149495893	149551551	5q32	5q32		600505	CSNK1A1	"Casein kinase-1, alpha-1 polypeptide"	CSNK1A1	1452	ENSG00000113712	previously assigned to 13q13		Csnk1a1 (MGI:1934950)			
chr5	149730251	149857860	5q33	5q32		608886	"PPARGC1B, PGC1B, PERC"	"Peroxisome proliferator-activated receptor-gamma, coactivator 1, beta"	PPARGC1B	133522	ENSG00000155846		"{Obesity, variation in}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Ppargc1b (MGI:2444934)			
chr5	149732824	149732889	5q33.1	5q32		611957	"MIR378, MIRN378"	Micro RNA 378	MIR378A	494327							
chr5	149857955	149944792	5q31.2-q34	5q32		180071	"PDE6A, PDEA, RP43"	"Phosphodiesterase-6A, cGMP-specific, rod, alpha"	PDE6A	5145	ENSG00000132915		"Retinitis pigmentosa 43, 613810 (3)"	Pde6a (MGI:97524)			
chr5	149960736	149987399	5q32-q33.1	5q32		606718	"SLC26A2, DTD, DTDST, D5S1708, EDM4"	"Solute carrier family 26 (sulfate transporter), member 2 (diastrophic dysplasia sulfate transporter)"	SLC26A2	1836	ENSG00000155850	distal to APC	"Achondrogenesis Ib, 600972 (3), Autosomal recessive; Atelosteogenesis, type II, 256050 (3), Autosomal recessive; De la Chapelle dysplasia, 256050 (3), Autosomal recessive; Diastrophic dysplasia, 222600 (3), Autosomal recessive; Diastrophic dysplasia, broad bone-platyspondylic variant, 222600 (3), Autosomal recessive; Epiphyseal dysplasia, multiple, 4, 226900 (3), Autosomal recessive"	Slc26a2 (MGI:892977)			
chr5	150021526	150022052	5q33-qter	5q32		180464	RPS20B	Ribosomal protein S20B	RPS20P4	6226		?pseudogene					
chr5	150053290	150113371	5q32	5q32		164770	"CSF1R, FMS, HDLS"	Colony-stimulating factor-1 receptor; oncogene FMS (McDonough feline sarcoma)	CSF1R	1436	ENSG00000182578	FMS2 is 5' end	"Leukoencephalopathy, diffuse hereditary, with spheroids, 221820 (3), Autosomal dominant"	Csf1r (MGI:1339758)			
chr5	150113838	150155858	5q32	5q32		173410	"PDGFRB, PDGFR, IBGC4, IMF1, PENTT, KOGS"	"Platelet-derived growth factor receptor, beta polypeptide"	PDGFRB	5159	ENSG00000113721	"fusion gene with ETV6, HIP1, RABPT5, or H4 in chronic myeloproliferative disorders"	"Basal ganglia calcification, idiopathic, 4, 615007 (3), Autosomal dominant; Kosaki overgrowth syndrome, 616592 (3), Autosomal dominant; Myeloproliferative disorder with eosinophilia, 131440 (4), Autosomal dominant; Myofibromatosis, infantile, 1, 228550 (3), Autosomal dominant; Premature aging syndrome, Penttinen type, 601812 (3), Autosomal dominant"	Pdgfrb (MGI:97531)			
chr5	150166780	150184557	5q31-q33	5q32		600746	CDX1	Caudal type homeo box transcription factor 1	CDX1	1044	ENSG00000113722	100kb distal to CSF1R		Cdx1 (MGI:88360)			
chr5	150189860	150211071	5q31-q32	5q32		606205	"SLC6A7, PROT"	"Solute carrier family 6 (neurotransmitter transporter, L-proline), member 7"	SLC6A7	6534	ENSG00000011083			Slc6a7 (MGI:2147363)			
chr5	150219490	150289839	5q32	5q32		114078	"CAMK2A, KIAA0968, CAMKA, MRD53"	Calcium/calmodulin-dependent protein kinase II-alpha	CAMK2A	815	ENSG00000070808		"Mental retardation, autosomal dominant 53, 617798 (3), Autosomal dominant"	Camk2a (MGI:88256)			
chr5	150296338	150302961	5q32	5q32		610009	ARSI	Arylsulfatase I	ARSI	340075	ENSG00000183876			Arsi (MGI:2670959)			
chr5	150357638	150400307	5q32-q33.1	5q32-q33		606847	"TCOF1, MFD1, TCS1"	Treacle	TCOF1	6949	ENSG00000070814	prox. to SPARC	"Treacher Collins syndrome 1, 154500 (3), Autosomal dominant"	Tcof1 (MGI:892003)			
chr5	150400000	177100000	5q33.1-q35.2			613269	"FECD5, FCD3"	"Corneal dystrophy, Fuchs endothelial, 5"		100380874		flanked by D5S470 and D5S2108	"Corneal dystrophy, Fuchs endothelial, 5, 613269 (2)"				
chr5	150401636	150412935	5q32	5q33.1		142790	"CD74, DHLAG"	CD74 antigen (invariant polypeptide of major histocompatibility class II antigen-associated)	CD74	972	ENSG00000019582			Cd74 (MGI:96534)			
chr5	150444228	150449755	5q32	5q33.1		130620	"RPS14, EMTB"	Ribosomal protein S14	RPS14	6208	ENSG00000164587		"Macrocytic anemia, refractory, due to 5q deletion, somatic, 153550 (3)"	Rps14 (MGI:98107)			
chr5	150485782	150558210	5q32-q33.3	5q33.1		600853	"NDST1, HSST, MRT46"	N-deacetylase/N-sulfotransferase (heparan sulfate-N-deacetylase/N-sulfotransferase)	NDST1	3340	ENSG00000070614		"Mental retardation, autosomal recessive 46, 616116 (3), Autosomal recessive"	Ndst1 (MGI:104719)			
chr5	150586025	150659229	5q33.1	5q33.1		608155	SYNPO	Synaptopodin	SYNPO	11346	ENSG00000171992			Synpo (MGI:1099446)			
chr5	150660840	150679367	5q31	5q33.1		610735	"MYOZ3, FRP3"	Myozenin 3	MYOZ3	91977	ENSG00000164591			Myoz3 (MGI:2179296)			
chr5	150690789	150701106	5q33.1	5q33.1		612430	RBM22	RNA-binding motif protein 22	RBM22	55696	ENSG00000086589			Rbm22 (MGI:1914060)			
chr5	150708746	150759094	5q33.1	5q33.1		614758	"DCTN4, P62, DYN4"	Dynactin 4	DCTN4	51164	ENSG00000132912			Dctn4 (MGI:1914915)			
chr5	150777945	150796735	5q32	5q33.1		608324	"SMIM3, NID67"	Small integral membrane protein 3	SMIM3	85027	ENSG00000256235			Smim3 (MGI:1917088)			
chr5	150846522	150902401	5q33.1	5q33.1		608212	"IRGM, LRG47, IFI1, IBD19"	"Immunity-related GTPase family, M"	IRGM	345611	ENSG00000237693		"{Inflammatory bowel disease (Crohn disease) 19}, 612278 (3); {Mycobacterium tuberculosis, protection against}, 607948 (3)"	Irgm2 (MGI:1926262)			
chr5	150892957	150904982	5q33.1	5q33.1		612429	ZNF300	Zinc finger protein 300	ZNF300	91975	ENSG00000145908						
chr5	151020411	151028992	5q32-q33.1	5q33.1		138321	GPX3	"Glutathione peroxidase-3, plasma"	GPX3	2878	ENSG00000211445			Gpx3 (MGI:105102)			
chr5	151029942	151087659	5q32-q33.1	5q33.1		607714	"TNIP1, NAF1, KIAA0113"	TNFAIP3-interacting protein 1	TNIP1	10318	ENSG00000145901			Tnip1 (MGI:1926194)			
chr5	151100705	151157881	5q32-q34	5q33.1		114070	"ANXA6, CBP68"	Annexin A6 (calcium-binding protein p68)	ANXA6	309	ENSG00000197043			Anxa6 (MGI:88255)			
chr5	151253051	151270393	5q31.3-q33.1	5q33.1		613109	GM2A	GM2 ganglioside activator protein	GM2A	2760	ENSG00000196743	pseudogene on chr.3	"GM2-gangliosidosis, AB variant, 272750 (3), Autosomal recessive"	Gm2a (MGI:95762)			
chr5	151314977	151347589	5q33.1	5q33.1		608331	"SLC36A2, PAT2"	"Solute carrier family 36 (proton/amino acid symporter), member 2"	SLC36A2	153201	ENSG00000186335		"Hyperglycinuria, 138500 (3), Autosomal dominant; Iminoglycinuria, digenic, 242600 (3), Autosomal recessive, Digenic recessive"	Slc36a2 (MGI:1891430)			
chr5	151411343	151556317	5q31-q33	5q33.1		606561	"SLC36A1, LYAAT1, PAT1"	"Solute carrier family 36 (proton/amino acid symporter), member 1 (lysosomal amino acid transporter 1)"	SLC36A1	206358	ENSG00000123643			Slc36a1 (MGI:2445299)			
chr5	151504091	151594821	5q32-q33	5q33.1		604269	"FAT2, MEGF1, SCA45"	"Fat tumor suppressor, Drosophila, homolog of, 2"	FAT2	2196	ENSG00000086570		"Spinocerebellar ataxia 45, 617769 (3), Autosomal dominant"	Fat2 (MGI:2685369)			
chr5	151661095	151687053	5q31.3-q32	5q33.1		182120	"SPARC, ON, OI17"	"Osteonectin (secreted protein, acidic, cysteine-rich)"	SPARC	6678	ENSG00000113140		"Osteogenesis imperfecta, type XVII, 616507 (3), Autosomal recessive"	Sparc (MGI:98373)			
chr5	151742821	151758648	5q32	5q33.1		602270	"ATOX1, HAH1"	"Antioxidant protein 1 (ATX, yeast, homolog of)"	ATOX1	475	ENSG00000177556			Atox1 (MGI:1333855)			
chr5	151771914	151805353	5q33.1	5q33.1		608431	"G3BP1, G3BP"	GTPase-activating protein SH3 domain-binding protein 1	G3BP1	10146	ENSG00000145907			G3bp1 (MGI:1351465)			
chr5	151822512	151924835	5q32	5q33.1		138491	"GLRA1, STHE, HKPX1"	"Glycine receptor, alpha-1 polypeptide"	GLRA1	2741	ENSG00000145888		"Hyperekplexia, hereditary 1, autosomal dominant or recessive, 149400 (3), Autosomal recessive, Autosomal dominant"	Glra1 (MGI:95747)			
chr5	152391540	152405278	5q33.1	5q33.1		605108	"NMUR2, NMU2R, FM4"	Neuromedin U receptor 2	NMUR2	56923	ENSG00000132911			Nmur2 (MGI:2441765)			
chr5	153490523	153813872	5q33	5q33.2		138248	"GRIA1, GLUR1"	"Glutamate receptor, ionotropic, AMPA 1"	GRIA1	2890	ENSG00000155511			Gria1 (MGI:95808)			
chr5	154038958	154057453	5q32-q33.3	5q33.2		600491	MFAP3	Microfibrillar-associated protein-3	MFAP3	4238	ENSG00000037749			Mfap3 (MGI:1924068)			
chr5	154190734	154420983	5q33.2	5q33.2		608043	"GALNT10, GalNAcT10"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 10	GALNT10	55568	ENSG00000164574			Galnt10 (MGI:1890480)			
chr5	154445956	154461052	5q33.2	5q33.2		610398	SAP30L	SAP30-like protein	SAP30L	79685	ENSG00000164576			Sap30l (MGI:1354709)			
chr5	154474971	154478263	5q33.2	5q33.2		602406	"HAND1, EHAND"	Heart- and neural crest derivatives-expressed 1	HAND1	9421	ENSG00000113196			Hand1 (MGI:103577)			
chr5	154682662	154817606	5q33.2	5q33.2		612059	"LARP1, LARP, KIAA0731"	"La ribonucleoprotein domain family, member 1"	LARP1	23367	ENSG00000155506	incorrectly mapped to chromosome 10		Larp1 (MGI:1890165)			
chr5	154857951	154876791	5q31-q33	5q33.2		603731	"CNOT8, CALIF, POP2"	"CCR4-NOT transcription complex, subunit 8"	CNOT8	9337	ENSG00000155508			Cnot8 (MGI:1916375)			
chr5	154887415	154938215	5q33.2	5q33.2		607005	GEMIN5	GEM-associated protein 5	GEMIN5	25929	ENSG00000082516			Gemin5 (MGI:2449311)			
chr5	154941072	154969410	5q33	5q33.2		611835	MRPL22	Mitochondrial ribosomal protein L22	MRPL22	29093	ENSG00000082515			Mrpl22 (MGI:1333794)			
chr5	155013754	155018131	5q33.1	5q33.2		609184	KIF4B	Kinesin family member 4B	KIF4B	285643	ENSG00000226650						
chr5	155728635	156767787	5q33	5q33.2-q33.3		601411	"SGCD, SGD, LGMD2F, CMD1L"	"Sarcoglycan, delta (35kD dystrophin-associated glycoprotein)"	SGCD	6444	ENSG00000170624	mutant in Syrian hamster cardiomyopathy	"Cardiomyopathy, dilated, 1L, 606685 (3); Muscular dystrophy, limb-girdle, type 2F, 601287 (3), Autosomal recessive"	Sgcd (MGI:1346525)			
chr5	156919281	156963254	5q33.2	5q33.3		610096	"TIMED4, TIM4, SMUCKLER"	T-cell immunoglobulin and mucin domains-containing protein 4	TIMD4	91937	ENSG00000145850			Timd4 (MGI:2445125)			
chr5	157028382	157069632	5q33.2	5q33.3		606518	"HAVCR1, HAVCR"	Hepatitis A virus cellular receptor 1	HAVCR1	26762	ENSG00000113249						
chr5	157085831	157109236	5q33.2	5q33.3		606652	TIM3	T-cell immunoglobulin- and mucin-domain-containing molecule	HAVCR2	84868	ENSG00000135077			Havcr2 (MGI:2159682)			
chr5	157138439	157142909	5q33.3	5q33.3		605045	"MED7, CRSP9, CRSP33"	Mediator complex subunit 7	MED7	9443	ENSG00000155868			Med7 (MGI:1913463)			
chr5	157180895	157255184	5q32	5q33.3		186973	"ITK, EMT, LPFS1"	T-cell-specific tyrosine kinase; homolog of mouse T-cell itk/tsk tyrosine kinase	ITK	3702	ENSG00000113263		"Lymphoproliferative syndrome 1, 613011 (3), Autosomal recessive"	Itk (MGI:96621)			
chr5	157266079	157395597	5q33.3	5q33.3		606323	CYFIP2	Cytoplasmic FMRP interacting protein 2	CYFIP2	26999	ENSG00000055163			Cyfip2 (MGI:1924134)			
chr5	157460018	157474721	5q33	5q33.3		609383	"NIPAL4, ICHYN, ARCI6"	NIPA-like domain-containing 4	NIPAL4	348938	ENSG00000172548		"Ichthyosis, congenital, autosomal recessive 6, 612281 (3), Autosomal recessive"	Nipal4 (MGI:2444671)			
chr5	157477303	157575822	5q32-q33	5q33.3		603640	"ADAM19, MLTNB"	"A disintegrin and metalloproteinase domain-19 (meltrin-beta, mouse, homolog of)"	ADAM19	8728	ENSG00000135074			Adam19 (MGI:105377)			
chr5	157743694	157760708	5q33.3	5q33.3		617910	LSM11	"Lsm11, U7 small nuclear RNA-associated protein"	LSM11	134353	ENSG00000155858			Lsm11 (MGI:1919540)			
chr5	157785742	157859174	5q33.3	5q33.3		607265	"CLINT1, EPN4, EPNR, KIAA0171"	Clathrin interactor 1 (epsin 4)	CLINT1	9685	ENSG00000113282			Clint1 (MGI:2144243)			
chr5	158695914	159099761	5q34	5q33.3		164343	"EBF, OLF1"	Early B-cell factor (olfactory neuronal transcription factor 1)	EBF1	1879	ENSG00000164330			Ebf1 (MGI:95275)			
chr5	159263066	159286039	5q33.3	5q33.3		609867	UBLCP1	Ubiquitin-like domain-containing CTD phosphatase 1	UBLCP1	134510	ENSG00000164332			Ublcp1 (MGI:1933105)			
chr5	159314782	159330472	5q33.3	5q33.3		161561	"IL12B, NKSF2, IMD29"	"Interleukin-12B (natural killer cell stimulatory factor-2, cytotoxic lymphocyte maturation factor-2, p40)"	IL12B	3593	ENSG00000113302	between GLR1 and GABRA1	"Immunodeficiency 29, mycobacteriosis, 614890 (3), Autosomal recessive"	Il12b (MGI:96540)			
chr5	159916732	159989204	5q33	5q33.3		104220	ADRA1B	"Adrenergic, alpha-1B-, receptor"	ADRA1B	147	ENSG00000170214			Adra1b (MGI:104774)			
chr5	160009099	160065544	5q32-q33.2	5q33.3		601963	"TTC1, TPR1"	Tetratricopeptide repeat domain-1	TTC1	7265	ENSG00000113312			Ttc1 (MGI:1914077)			
chr5	160043537	160120700	5q33.3	5q33.3		617823	PWWP2A	PWWP domain-containing protein 2A	PWWP2A	114825	ENSG00000170234			Pwwp2a (MGI:1918052)			
chr5	160187366	160238721	5q23-q35	5q33.3		600422	"FABP6, ILLBP"	"Fatty acid-binding protein 6, ileal (gastrotropin)"	FABP6	2172	ENSG00000170231			Fabp6 (MGI:96565)			
chr5	160393147	160400096	5q33.3	5q33.3		615253	"C5orf54, ZBED8, BUSTER3"	Chromosome 5 open reading frame 54	ZBED8	63920	ENSG00000221886						
chr5	160421806	160428743	5q33	5q33.3		604147	"PTTG1, EAP1, TUTR1"	Pituitary tumor-transforming gene 1	PTTG1	9232	ENSG00000164611			Pttg1 (MGI:1353578)			
chr5	160485351	160485449	5q33.3	5q33.3		610566	"MIR146A, MIRN146A"	Micro RNA 146A	MIR146A	406938							
chr5	160500000	177100000	5q34-q35.2			608036	NIDDM4	"Diabetes mellitus, noninsulin-dependent, 4"		100188782			"{Diabetes mellitus, noninsulin-dependent}, 125853 (2), Autosomal dominant"				
chr5	161288428	161548123	5q34-q35	5q34		600232	"GABRB2, ICEE2"	"Gamma-aminobutyric acid (GABA) A receptor, beta-2"	GABRB2	2561	ENSG00000145864		"Epileptic encephalopathy, infantile or early childhood, 2, 617829 (3), Autosomal dominant"	Gabrb2 (MGI:95620)			
chr5	161685651	161702591	5q31.1-q35	5q34		137143	GABRA6	"Gamma-aminobutyric acid (GABA) A receptor, alpha-6"	GABRA6	2559	ENSG00000145863			Gabra6 (MGI:95618)			
chr5	161847190	161899958	5q34-q35	5q34		137160	"GABRA1, EJM5, ECA4, EIEE19"	"Gamma-aminobutyric acid (GABA) A receptor, alpha-1"	GABRA1	2554	ENSG00000022355	in same 200kb as GABRG2	"{Epilepsy, childhood absence, susceptibility to, 4}, 611136 (3); {Epilepsy, juvenile myoclonic, susceptibility to, 5}, 611136 (3); Epileptic encephalopathy, early infantile, 19, 615744 (3), Autosomal dominant"	Gabra1 (MGI:95613)			
chr5	162067641	162155538	5q34	5q34		137164	"GABRG2, GEFSP3, CAE2, ECA2"	"Gamma-aminobutyric acid (GABA) A receptor, gamma-2"	GABRG2	2566	ENSG00000113327	in alpha/beta/gamma cluster	"{Epilepsy, childhood absence, susceptibility to, 2}, 607681 (3), Autosomal dominant; Epilepsy, generalized, with febrile seizures plus, type 3, 611277 (3), Autosomal dominant; Febrile seizures, familial, 8, 611277 (3), Autosomal dominant"	Gabrg2 (MGI:95623)			
chr5	163437570	163445015	5q32-q34	5q34		601578	CCNG1	Cyclin G1	CCNG1	900	ENSG00000113328			Ccng1 (MGI:102890)			
chr5	163460510	163491944	5q33.2	5q34		600936	HMMR	Hyaluronan-mediated motility receptor (RHAMM)	HMMR	3161	ENSG00000072571		"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant"	Hmmr (MGI:104667)			
chr5	166979065	168264158	5q34	5q34		610119	"TENM2, ODZ2, TNM2, KIAA1127"	Teneurin transmembrane protein 2	TENM2	57451	ENSG00000145934			Tenm2 (MGI:1345184)			
chr5	168292059	168472302	5q34-q35.2	5q34		610533	"WWC1, KIBRA, KIAA0869, MEMRYQTL"	"WW, C2, and coiled-coil domain-containing 1"	WWC1	23286	ENSG00000113645		"[Memory, enhanced, QTL], 615602 (3)"	Wwc1 (MGI:2388637)			
chr5	168486457	168519305	5q34	5q34		107820	"RARS, HLD9"	Arginyl-tRNA synthetase	RARS	5917	ENSG00000113643		"Leukodystrophy, hypomyelinating, 9, 616140 (3), Autosomal recessive"	Rars (MGI:1914297)			
chr5	168555622	168579608	5q35	5q34		606161	PANK3	Pantothenate kinase 3	PANK3	79646	ENSG00000120137			Pank3 (MGI:2387464)			
chr5	168560895	168560972	5q34	5q34		613187	"MIR103-1, MIRN103-1"	Micro RNA 103-1	MIR103A1	406895							
chr5	168661732	169301128	5q35	5q34-q35		603745	"SLIT3, SLIL2, MEGF5"	"Slit, Drosophila, homolog of, 3"	SLIT3	6586	ENSG00000184347			Slit3 (MGI:1315202)			
chr5	168768145	168768254	5q34	5q34		616771	MIR218-2	Micro RNA 218-2	MIR218-2	407001		in intron of SLIT3					
chr5	169000000	181538259	5q35			208100	"AMCN, AMCN1"	"Arthrogryposis multiplex congenital, neurogenic"	AMCN	261			"Arthrogryposis multiplex congenita, neurogenic, 208100 (2), Autosomal recessive"				
chr5	169000000	181538259	5q35			118840	CHR	Chromate resistance (sulfate transport)									
chr5	169583633	169604777	5q35.1	5q35.1		616401	"SPDL1, CCDC99, SPINDLY"	Spindly apparatus coiled-coil protein 1	SPDL1	54908	ENSG00000040275			Spdl1 (MGI:1917635)			
chr5	169637246	170083381	5q35.1	5q35.1		603122	"DOCK2, IMD40"	Dedicator of cytokinesis 2	DOCK2	1794	ENSG00000134516		"Immunodeficiency 40, 616433 (3), Autosomal recessive"	Dock2 (MGI:2149010)			
chr5	170105896	170109724	5q34	5q35.1		601093	"FOXI1, FKHL10, FREAC6"	Forkhead box I1	FOXI1	2299	ENSG00000168269	some patients have digenic mutations with SLC26A4	"Enlarged vestibular aqueduct, 600791 (3), Autosomal recessive"	Foxi1 (MGI:1096329)			
chr5	170246232	170297841	5q33.1-qter	5q35.1		601603	"LCP2, SLP76"	Lymphocyte cytosolic protein-2 (SH2 domain-containing leukocyte protein of 76kD)	LCP2	3937	ENSG00000043462			Lcp2 (MGI:1321402)			
chr5	170378160	170389676	5q34	5q35.1		603951	KCNMB1	"Potassium large conductance calcium-activated channel, subfamily M, beta member 1"	KCNMB1	3779	ENSG00000145936		"{Hypertension, diastolic, resistance to}, 608622 (3), Autosomal dominant"	Kcnmb1 (MGI:1334203)			
chr5	170782840	170814046	5q32-q33	5q35.1		602729	GABRP	"Gamma-aminobutyric acid receptor, pi"	GABRP	2568	ENSG00000094755			Gabrp (MGI:2387597)			
chr5	170861881	171300014	5q34	5q35.1		606141	RANBP17	RAN-binding protein 17	RANBP17	64901	ENSG00000204764			Ranbp17 (MGI:1929706)			
chr5	171309283	171312133	5q35.1	5q35.1		604640	"TLX3, HOX11L2, RNX"	"T-cell leukemia, homeobox 3"	TLX3	30012	ENSG00000164438	activated in T-cell ALL		Tlx3 (MGI:1351209)			
chr5	171387115	171410883	5q35	5q35.1		164040	NPM1	"Nucleophosmin 1 (nucleolar phosphoprotein B23, numatrin)"	NPM1	4869	ENSG00000181163	fused with RARA in APL	"Leukemia, acute myeloid, somatic, 601626 (3)"	Npm1 (MGI:106184)			
chr5	171419662	171457625	5q34	5q35.1		603726	FGF18	Fibroblast growth factor-18	FGF18	8817	ENSG00000156427			Fgf18 (MGI:1277980)			
chr5	171861548	172009603	5q35.1	5q35.1		605651	"FBXW11, FBXW1B, BTRC2, BTRCP2"	F-box and WD40 domain protein 11	FBXW11	23291	ENSG00000072803			Fbxw11 (MGI:2144023)			
chr5	172042069	172188341	5q35.1	5q35.1		603919	"STK10, LOK"	Serine/threonine protein kinase-10	STK10	6793	ENSG00000072786			Stk10 (MGI:1099439)			
chr5	172209644	172283796	5q35	5q35.1		610174	"UBTD2, DCUBP, MGC30022"	Ubiquitin domain-containing protein 2	UBTD2	92181	ENSG00000168246			Ubtd2 (MGI:2444752)			
chr5	172325180	172454522	5q35.1	5q35.1		613293	"SH3PXD2B, TKS4, KIAA1295, FTHS"	SH3 and PX domains-containing protein 2B	SH3PXD2B	285590	ENSG00000174705		"Frank-ter Haar syndrome, 249420 (3), Autosomal recessive"	Sh3pxd2b (MGI:2442062)			
chr5	172641265	172691539	5q31	5q35.1		615893	"NEURL1B, NEUR2"	Neuralized E3 ubiquitin protein ligase 1B	NEURL1B	54492	ENSG00000214357			Neurl1b (MGI:3643092)			
chr5	172768089	172771199	5q34	5q35.1		600714	"DUSP1, CL100, PTPN10"	Dual specificity phosphatase-1	DUSP1	1843	ENSG00000120129			Dusp1 (MGI:105120)			
chr5	172983759	173034896	5q35.1	5q35.1		603931	"ATP6V0E, ATP6H"	"ATPase, H+ transporting, lysosomal 9kD V0 subunit e"	ATP6V0E1	8992	ENSG00000113732	previously mapped to Chr.2		Atp6v0e (MGI:1328318)			
chr5	173020725	173020928	5q35.1	5q35.1		611331	SNORA74B	"Small nucleolar RNA, H/ACA box, 74B"	SNORA74B	677841		in intron 3 of ATP6V0E1					
chr5	173056348	173139287	5q35.1	5q35.1		617109	"CREBRF, LRF, C5orf41"	CREB3 recruitment factor	CREBRF	153222	ENSG00000164463			Crebrf (MGI:1924378)			
chr5	173144441	173164386	5q35.1	5q35.1		603291	"BNIP1, NIP1"	BCL2/adenovirus E1B 19kD protein-interacting protein 1	BNIP1	662	ENSG00000113734			Bnip1 (MGI:109328)			
chr5	173232103	173235320	5q34	5q35.1		600584	"NKX2-5, NKX2E, CSX, CHNG5, VSD3, HLHS2"	NK2 homeobox-5 gene	NKX2-5	1482	ENSG00000183072	near border with 5q35	"Atrial septal defect 7, with or without AV conduction defects, 108900 (3), Autosomal dominant; Conotruncal heart malformations, variable, 217095 (3); Hypoplastic left heart syndrome 2, 614435 (3), Autosomal dominant; Hypothyroidism, congenital nongoitrous, 5, 225250 (3), Autosomal dominant; Tetralogy of Fallot, 187500 (3), Autosomal dominant; Ventricular septal defect 3, 614432 (3), Autosomal dominant"	Nkx2-5 (MGI:97350)			
chr5	173300000	177100000	5q35.2			612886	MENOQ4	"Menopause, natural, age at, QTL4"		100302519		"associated with rs365132, rs7718874, rs402511, rs691141, rs2278493"	"{Menopause, natural, age at, QTL4}, 612886 (2)"				
chr5	173314722	173329502	5q35.1	5q35.2		603665	"STC2, STCRP"	Stanniocalcin 2	STC2	8614	ENSG00000113739			Stc2 (MGI:1316731)			
chr5	173607144	173617071	5q35.2	5q35.2		616745	"BOD1, FAM44B"	Biorientation of chromosomes in cell division 1	BOD1	91272	ENSG00000145919			Bod1 (MGI:1916806)			
chr5	173888327	173960990	5q21	5q35.2		610607	"CPEB4, KIAA1673"	Cytoplasmic polyadenylation element-binding protein 4	CPEB4	80315	ENSG00000113742			Cpeb4 (MGI:1914829)			
chr5	174045603	174109178	5q35.2	5q35.2		616752	"HMP19, NSG2"	"Hypothalamus golgi apparatus-expressed protein, 19kD"	NSG2	51617	ENSG00000170091			Nsg2 (MGI:1202070)			
chr5	174724495	174730898	5q34-q35	5q35.2		123101	"MSX2, CRS2, HOX8"	"msh, Drosophila, homeo box homolog of, 2"	MSX2	4488	ENSG00000120149		"Craniosynostosis 2, 604757 (3), Autosomal dominant; Parietal foramina 1, 168500 (3), Autosomal dominant; Parietal foramina with cleidocranial dysplasia, 168550 (3), Autosomal dominant"	Msx2 (MGI:97169)			
chr5	175440037	175444217	5q35.1	5q35.2		126449	DRD1	Dopamine receptor D1	DRD1	1812	ENSG00000184845	same 300kb fragment as GRL		Drd1 (MGI:99578)			
chr5	175478497	175529741	5q35.2	5q35.2		615569	SFXN1	Sideroflexin 1	SFXN1	94081	ENSG00000164466			Sfxn1 (MGI:2137677)			
chr5	175796538	175884020	5q35.2	5q35.2		605033	"CPLX2, CPX2"	Complexin 2	CPLX2	10814	ENSG00000145920			Cplx2 (MGI:104726)			
chr5	175959530	176034904	5q35.2	5q35.2		606929	"THOC3, TEX1"	"THO complex 3 (Tex1, yeast, homolog of)"	THOC3	84321	ENSG00000051596			Thoc3 (MGI:1920916)			
chr5	176383936	176388926	5q35.2	5q35.2		612861	"NOP15, HSPC111"	"Nop16, S. cerevisiae, homolog of"	NOP16	51491	ENSG00000048162			Nop16 (MGI:107862)			
chr5	176392454	176416568	5q35.2	5q35.2		118970	CLTB	"Clathrin, light polypeptide (Lcb)"	CLTB	1212	ENSG00000175416	previously mapped to chr. 4		Cltb (MGI:1921575)			
chr5	176448327	176510073	5q35.2	5q35.2		616935	"FAF2, ETEA, UBXD8, KIAA0887"	"Fas-associated factor family, member 2"	FAF2	23197	ENSG00000113194			Faf2 (MGI:1923827)			
chr5	176595801	176610129	5q35.2	5q35.2		611239	"GPRIN1, GRIN1, KIAA1893"	G protein-regulated inducer of neurite outgrowth 1	GPRIN1	114787	ENSG00000169258			Gprin1 (MGI:1349455)			
chr5	176620083	176630560	5q35	5q35.2		602569	SNCB	"Synuclein, beta"	SNCB	6620	ENSG00000074317		"Dementia, Lewy body, 127750 (3), Autosomal dominant"	Sncb (MGI:1889011)			
chr5	176810558	176880897	5q35.2	5q35.2		607869	"UNC5A, UNC5H1"	"UNC5, C. elegans, homolog of, A"	UNC5A	90249	ENSG00000113763			Unc5a (MGI:894682)			
chr5	176880868	176899372	5q35.2	5q35.2		142570	HK3	"Hexokinase-3, white cell"	HK3	3101	ENSG00000160883			Hk3 (MGI:2670962)			
chr5	176905004	177022639	5q35	5q35.2		609433	"UIMC1, RAP80"	Ubiquitin interaction motif containing 1	UIMC1	51720	ENSG00000087206			Uimc1 (MGI:103185)			
chr5	177022679	177081188	5q35.2	5q35.2		605308	"ZNF346, JAZ"	Zinc finger protein 346	ZNF346	23567	ENSG00000113761			Zfp346 (MGI:1349417)			
chr5	177086871	177098141	5q35.1-qter	5q35.2		134935	FGFR4	Fibroblast growth factor receptor-4	FGFR4	2264	ENSG00000160867	distal to DRD1	{Cancer progression/metastasis} (3)	Fgfr4 (MGI:95525)			
chr5	177131834	177300212	5q35	5q35.3		606681	"NSD1, ARA267, STO, SOTOS1"	Nuclear receptor binding SET domain protein 1	NSD1	64324	ENSG00000165671	fusion gene with NUP98 in AML	"Leukemia, acute myeloid, 601626 (1), Autosomal dominant; Sotos syndrome 1, 117550 (3), Autosomal dominant"	Nsd1 (MGI:1276545)			
chr5	177301189	177303743	5q35.3	5q35.3		612415	RAB24	Ras-associated protein 24	RAB24	53917	ENSG00000169228			Rab24 (MGI:105065)			
chr5	177303761	177306958	5q35.3	5q35.3		605733	"PRELID1, PRELI, PX19"	PRELI domain-containing protein 1	PRELID1	27166	ENSG00000169230			Prelid1 (MGI:1913744)			
chr5	177305499	177312290	5q35.3	5q35.3		609450	"MXD3, MAD3"	MAX dimerization protein 3	MXD3	83463	ENSG00000213347			Mxd3 (MGI:104987)			
chr5	177357670	177372600	5q35.3	5q35.3		602513	RGS14	Regulator of G protein signaling 14	RGS14	10636	ENSG00000169220			Rgs14 (MGI:1859709)			
chr5	177384430	177412020	5q35	5q35.3		182309	"SLC34A1, SLC17A2, NPT2, NPHLOP1, FRTS2, HCINF2"	"Solute carrier family 34 (sodium phosphate cotransporter), member 1"	SLC34A1	6569	ENSG00000131183	mutation identified in 1 FRTS2 family	"?Fanconi renotubular syndrome 2, 613388 (3), Autosomal recessive; Hypercalcemia, infantile, 2, 616963 (3), Autosomal recessive; Nephrolithiasis/osteoporosis, hypophosphatemic, 1, 612286 (3), Autosomal dominant"	Slc34a1 (MGI:1345284)			
chr5	177400106	177400635	5q35.2	5q35.3		612812	PFN3	Profilin 3	PFN3	345456	ENSG00000196570			Pfn3 (MGI:2178800)			
chr5	177402137	177409575	5q33-qter	5q35.3		610619	"F12, HAF, HAE3"	Coagulation factor XII (Hageman factor)	F12	2161	ENSG00000131187		"Angioedema, hereditary, type III, 610618 (3), Autosomal dominant; Factor XII deficiency, 234000 (3), Autosomal recessive"	F12 (MGI:1891012)			
chr5	177426495	177442848	5q35	5q35.3		600869	"GRK6, GPRK6"	G protein-coupled receptor kinase 6	GRK6	2870	ENSG00000198055			Grk6 (MGI:1347078)			
chr5	177456611	177480367	5q35.3	5q35.3		126660	DBN1	Drebrin-1	DBN1	1627	ENSG00000113758			Dbn1 (MGI:1931838)			
chr5	177483393	177497604	5q35.3	5q35.3		605903	"PDLIM7, ENIGMA"	PDZ and LIM domain 7 (enigma)	PDLIM7	9260	ENSG00000196923			Pdlim7 (MGI:1914649)			
chr5	177501903	177510507	5q35.3	5q35.3		611435	"DOK3, DOKL"	Docking protein 3	DOK3	79930	ENSG00000146094			Dok3 (MGI:1351490)			
chr5	177511576	177517325	5q35.3	5q35.3		608170	"DDX41, ABS, MPLPF"	DEAD/H box 41	DDX41	51428	ENSG00000183258		"{Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to}, 616871 (3), Autosomal dominant"	Ddx41 (MGI:1920185)			
chr5	177519788	177554584	5q35.3	5q35.3		615813	"FAM193B, IRIZIO, KIAA1931"	"Family with sequence similarity 193, member B"	FAM193B	54540	ENSG00000146067						
chr5	177600101	177610346	5q35.2-q35.3	5q35.3		604327	"B4GALT7, XGALT1, XGPT1, EDSSPD1"	"Beta-1,4-galactosyltransferase 7"	B4GALT7	11285	ENSG00000027847		"Ehlers-Danlos syndrome, spondylodysplastic type, 1, 130070 (3), Autosomal recessive"	B4galt7 (MGI:2384987)			
chr5	177992234	177996241	5q	5q35.3		601538	"PROP1, CPHD2"	"Prophet of Pit1, paired-like homeodomain transcription factor"	PROP1	5626	ENSG00000175325		"Pituitary hormone deficiency, combined, 2, 262600 (3), Autosomal recessive"	Prop1 (MGI:109330)			
chr5	178149462	178153959	5q35.3	5q35.3		606470	"NOLA2, NHP2, DKCB2"	"Nucleolar protein family A, member 2"	NHP2	55651	ENSG00000145912		"Dyskeratosis congenita, autosomal recessive 2, 613987 (3), Autosomal recessive"	Nhp2 (MGI:1098547)			
chr5	178207143	178232821	5q35.3	5q35.3		614683	"PHYKPL, AGXT2L2, PHLU"	5-phosphohydroxy-L-lysine phospho-lyase	PHYKPL	85007	ENSG00000175309	mutation identified in 1 PHLU patient	"[?Phosphohydroxylysinuria], 615011 (3)"	Phykpl (MGI:1920197)			
chr5	178237615	178590554	5q35	5q35.3		610043	COL23A1	"Collagen, type XXIII, alpha-1"	COL23A1	91522	ENSG00000050767			Col23a1 (MGI:2653243)			
chr5	178602663	178627052	5q35	5q35.3		607969	CLK4	CDC-like kinase 4	CLK4	57396	ENSG00000113240			Clk4 (MGI:1098551)			
chr5	178711520	178730701	5q35.3	5q35.3		602444	"TCF17, KID1"	Transcription factor-17	ZNF354A	6940	ENSG00000169131			Zfp354a (MGI:103172)			
chr5	178978326	178995122	5q35	5q35.3		604096	"GRM6, MGLUR6, CSNB1B"	"Glutamate receptor, metabotropic, 6"	GRM6	2916	ENSG00000113262		"Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270 (3), Autosomal recessive"	Grm6 (MGI:1351343)			
chr5	179110850	179345429	5q23	5q35.3		604539	"ADAMTS2, NPI, EDSDERMS"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 2 (procollagen I N-proteinase)"	ADAMTS2	9509	ENSG00000087116		"Ehlers-Danlos syndrome, dermatosparaxis type, 225410 (3), Autosomal recessive"	Adamts2 (MGI:1347356)			
chr5	179550550	179610025	5q35.3	5q35.3		610327	RUFY1	RUN and FYVE domains-containing protein 1	RUFY1	80230	ENSG00000176783			Rufy1 (MGI:2429762)			
chr5	179614177	179634783	5q35.3	5q35.3		601035	HNRPH1	Heterogeneous nuclear ribonucleoprotein H	HNRNPH1	3187	ENSG00000169045			Hnrnph1 (MGI:1891925)			
chr5	179678645	179731640	5q35	5q35.3		114217	CANX	Calnexin	CANX	821	ENSG00000127022			Canx (MGI:88261)			
chr5	179732849	179777285	5q35	5q35.3		605424	MAML1	"Mastermind, Drosophila, homolog of, 1"	MAML1	9794	ENSG00000161021			Maml1 (MGI:1890504)			
chr5	179793984	179796511	5q35	5q35.3		246530	LTC4S	Leukotriene C4 synthase	LTC4S	4056	ENSG00000213316		"Leukotriene C4 synthase deficiency, 614037 (1), Autosomal recessive"	Ltc4s (MGI:107498)			
chr5	179797596	179806976	5q35	5q35.3		604561	MGAT4B	"Alpha-1,3-mannosyl-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B"	MGAT4B	11282	ENSG00000161013			Mgat4b (MGI:2143974)			
chr5	179806387	179838077	5q35	5q35.3		601530	"SQSTM1, P62, PDB3, FTDALS3, NADGP, DMRV"	Sequestosome 1	SQSTM1	8878	ENSG00000161011		"Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 (3), Autosomal dominant; Myopathy, distal, with rimmed vacuoles, 617158 (3), Autosomal dominant; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145 (3), Autosomal recessive; Paget disease of bone 3, 167250 (3), Autosomal dominant"	Sqstm1 (MGI:107931)			
chr5	179837265	179858839	5q35.3	5q35.3		617154	"MRNIP, C5orf45"	MRN complex-interacting protein	MRNIP	51149	ENSG00000161010			Mrnip (MGI:1915317)			
chr5	180233593	180292070	5q35	5q35.3		602896	"MAPK9, PRKM9, JNK2"	Mitogen-activated protein kinase 9	MAPK9	5601	ENSG00000050748			Mapk9 (MGI:1346862)			
chr5	180300689	180353386	5q34-q35	5q35.3		603865	"GFPT2, GFAT2"	Glutamine: fructose-6-phosphate amidotransferase 2	GFPT2	9945	ENSG00000131459			Gfpt2 (MGI:1338883)			
chr5	180494372	180578404	5q35.3	5q35.3		608951	"CNOT6, CCR4, KIAA1194"	"CCR4-NOT transcription complex, subunit 6"	CNOT6	57472	ENSG00000113300			Cnot6 (MGI:2144529)			
chr5	180590104	180591486	5q35	5q35.3		606500	"SCGB3A1, HIN1"	"Secretoglobin, family 3A, member 1"	SCGB3A1	92304	ENSG00000161055			Scgb3a1 (MGI:1915912)			
chr5	180601505	180650297	5q35.3	5q35.3		136352	"FLT4, VEGFR3, PCL, LMPH1A"	fms-related tyrosine kinase-4 (vascular endothelial growth factor receptor 3)	FLT4	2324	ENSG00000037280		"Hemangioma, capillary infantile, somatic, 602089 (3); Lymphedema, hereditary, IA, 153100 (3), Autosomal dominant"	Flt4 (MGI:95561)			
chr5	180790540	180815634	5q35	5q35.3		160995	"MGAT1, GLYT1"	"Mannosyl (alpha-1,3-)-glycoprotein beta-1,2, N-acetylglucosaminyltransferase"	MGAT1	4245	ENSG00000131446			Mgat1 (MGI:96973)			
chr5	180843579	180861326	5q35.3	5q35.3		610281	ZFP62	Zinc finger protein 62	ZFP62	643836	ENSG00000196670			Zfp62 (MGI:99662)			
chr5	180899076	180952165	5q35.3	5q35.3		615606	"BTNL8, BTN9.2"	Butyrophilin-like protein 8	BTNL8	79908	ENSG00000113303						
chr5	180988844	181006726	5q35	5q35.3		606192	BTNL3	Butyrophilin-like protein 3	BTNL3	10917	ENSG00000168903						
chr5	181097069	181097141	5q35.3	5q35.3		612995	"TRV-CAC1-2, TRNAV2, TRV2"	Transfer RNA valine (CAC) 1-2	TRV-CAC1-2	7240							
chr5	181188853	181188924	5q35.3	5q35.3		189912	"TRP-TGG3-5, TRNAP3, TRP3"	Transfer RNA-Pro (TGG) 3-5	TRP-TGG3-1	7219							
chr5	181191686	181191757	5q35.3	5q35.3		189913	"TRT-TGT6-1, TRNAT1, TRT1"	Transfer RNA-Thr (TGT) 6-1	TRT-TGT6-1	7236							
chr5	181193923	181218331	5q35.3	5q35.3		609315	"TRIM7, GNIP"	Tripartite motif-containing protein 7	TRIM7	81786	ENSG00000146054			Trim7 (MGI:2137353)			
chr5	181218269	181218341	5q35.3	5q35.3		189921	"TRV-AAC1-4, TRNAV1, TRV1"	Transfer RNA valine (AAC) 1-4	TRV-AAC1-4	7239							
chr5	181221978	181222050	5q35.3	5q35.3		612996	"TRK-CTT2-4, TRNAK2, TRK2"	Transfer RNA lysine (CTT) 2-4	TRK-CTT2-3	790966							
chr5	181223262	181235807	5q35.3	5q35.3		610530	TRIM41	Tripartite motif-containing 41	TRIM41	90933	ENSG00000146063			Trim41 (MGI:2384814)			
chr5	181236927	181243905	5q35.3	5q35.3		176981	"GNB2L1, RACK1"	"Guanine nucleotide-binding protein, beta-2-like 1"	RACK1	10399	ENSG00000204628			Rack1 (MGI:101849)			
chr6	0	7100000	6p25			612558	CLLS4	"Leukemia, chronic lymphocytic susceptibility to, 4"		100270643		associated with rs872071	"{Leukemia, chronic lymphocytic susceptibility to, 4}, 612558 (2)"				
chr6	0	59800000	6p			122550	CSCI	Corticosterone side-chain isomerase		7944		?linked to MHC					
chr6	0	13400000	6pter-p24			612582	"DEL6pter, C6DELpter"	Chromosome 6pter-p24 deletion syndrome					"Chromosome 6pter-p24 deletion syndrome, 612582 (4), Isolated cases"				
chr6	0	25200000	6p25.3-p22.3			610294	INTLQ3	Intelligence quantitative trait locus 3		100462722			"{Intelligence QTL3}, 610294 (2)"				
chr6	0	7100000	6p25			608545	LRSL	Larsen-like syndrome		406214			"Larsen-like syndrome, 608545 (2), Isolated cases"				
chr6	292056	351354	6p25.3	6p25.3		616778	"DUSP22, LMWDSP2, MKPX, VHX, JKAP, JSP1"	Dual-specificity phosphatase 22	DUSP22	56940	ENSG00000112679			Dusp22 (MGI:1915926)			
chr6	391738	411442	6p25-p23	6p25.3		601900	"IRF4, LSIRF, SHEP8"	Interferon regulatory factor-4	IRF4	3662	ENSG00000137265	dysregulated in t(6;14)	"[Skin/hair/eye pigmentation, variation in, 8], 611724 (3)"	Irf4 (MGI:1096873)			
chr6	485137	693140	6p25.3	6p25.3		615329	"EXOC2, SEC5L1, SEC5"	Exocyst complex component 2	EXOC2	55770	ENSG00000112685			Exoc2 (MGI:1913732)			
chr6	655938	656963	6p25.3-p25.1	6p25.3		609713	HUS1B	"Hydroxyurea-sensitive 1, S. pombe, homolog of, B"	HUS1B	135458	ENSG00000188996			Hus1b (MGI:2671003)			
chr6	1312439	1314757	6p25	6p25.3		612788	"FOXQ1, HFH1"	Forkhead box Q1	FOXQ1	94234	ENSG00000164379			Foxq1 (MGI:1298228)			
chr6	1389833	1395596	6p25.3	6p25.3		603250	"FOXF2, FKHL6, FREAC2"	Forkhead box F2	FOXF2	2295	ENSG00000137273			Foxf2 (MGI:1347479)			
chr6	1605530	1607357	6p25	6p25.3		615976	"FOXCUT, LINC01379"	"FOXC1 upstream transcript, noncoding"	FOXCUT	101927703							
chr6	1610445	1613896	6p25	6p25.3		601090	"FOXC1, FKHL7, FREAC3, IRID1, RIEG3, ASGD3"	"Forkhead, Drosophila, homolog-like 7"	FOXC1	2296	ENSG00000054598		"Anterior segment dysgenesis 3, multiple subtypes, 601631 (3), Autosomal dominant; Axenfeld-Rieger syndrome, type 3, 602482 (3), Autosomal dominant"	Foxc1 (MGI:1347466)			
chr6	1623799	2245633	6p25	6p25.3		602884	GMDS	"GDP-mannose 4,6-dehydratase"	GMDS	2762	ENSG00000112699			Gmds (MGI:1891112)			
chr6	2765340	2785744	6p25.2	6p25.2		608196	"WRNIP1, WHIP"	Werner helicase-interacting protein 1	WRNIP1	56897	ENSG00000124535			Wrnip1 (MGI:1926153)			
chr6	2832331	2842048	6pter-p24	6p25.2		130135	"ELANH2, EI"	"Protease inhibitor 2 (anti-elastase), monocyte/neutrophil derived"	SERPINB1	1992	ENSG00000021355			Serpinb1a (MGI:1913472)			
chr6	2887264	2903317	6p25	6p25.2		601799	"PI9, CAP3, SERPINB9"	"Protease inhibitor 9, ovalbumin type"	SERPINB9	5272	ENSG00000170542			Serpinb9 (MGI:106603)			
chr6	2948158	2972164	6p25	6p25.2		173321	"SERPINB6, PI6, PTI, SPI3, DFNB91"	Protease inhibitor 6 (placental thrombin inhibitor)	SERPINB6	5269	ENSG00000124570	mutation identified in 1 DFNB91 family	"?Deafness, autosomal recessive 91, 613453 (3), Autosomal recessive"	Serpinb6a (MGI:103123)			
chr6	2999815	3019875	6p25	6p25.2		160998	"NQO2, NMOR2"	"NAD(P)H dehydrogenase, quinone 2 (NAD(P)H menadione oxidoreductase-1, dioxin-inducible-2)"	NQO2	4835	ENSG00000124588		"{?Breast cancer susceptibility}, 114480 (1), Autosomal dominant"	Nqo2 (MGI:104513)			
chr6	3063840	3115191	6p25.2	6p25.2		603453	"RIPK1, RIP1, RIP"	Receptor-interacting serine/threonine kinase 1	RIPK1	8737	ENSG00000137275			Ripk1 (MGI:108212)			
chr6	3118375	3153598	6p25	6p25.2		603156	BPHL	Biphenyl hydrolase-like	BPHL	670	ENSG00000137274			Bphl (MGI:1915271)			
chr6	3153665	3157548	6p25.2	6p25.2		615101	"TUBB2A, CDCBM5"	"Tubulin, beta-2A"	TUBB2A	7280	ENSG00000137267		"Cortical dysplasia, complex, with other brain malformations 5, 615763 (3), Autosomal dominant"	Tubb2a (MGI:107861)			
chr6	3224260	3227733	6p25.2	6p25.2		612850	"TUBB2B, CDCBM7"	"Tubulin, beta-2B"	TUBB2B	347733	ENSG00000137285	TUBB2A is 70kb telomeric to TUBB2B	"Cortical dysplasia, complex, with other brain malformations 7, 610031 (3), Autosomal dominant"	Tubb2b (MGI:1920960)			
chr6	3254324	3308223	6p25.2	6p25.2		617550	"PSMG4, PAC4, C6orf86"	Proteasome assembly chaperone 4	PSMG4	389362	ENSG00000180822			Psmg4 (MGI:1916916)			
chr6	3268972	3456573	6p25.2	6p25.2		611697	"SLC22A23, C6orf85"	"Solute carrier family 22, member 23"	SLC22A23	63027	ENSG00000137266			Slc22a23 (MGI:1920352)			
chr6	3831900	3851319	6p25.2	6p25.2		614686	"FAM60B, X5L"	"Family with sequence similarity 50, member B"	FAM50B	26240	ENSG00000145945			Fam50b (MGI:1351640)			
chr6	4021328	4064982	6p25.2	6p25.2		602338	"PRPF4B, PRP4"	"Pre-mRNA processing factor 4, yeast, homolog of, B"	PRPF4B	8899	ENSG00000112739			Prpf4b (MGI:109584)			
chr6	4115692	4135596	6p25.2	6p25.2		608024	"ECI2, PECI, DRS1"	Enoyl-CoA delta isomerase 2	ECI2	10455	ENSG00000198721			Eci2 (MGI:1346064)			
chr6	4706158	4955543	6p25.1	6p25.1		603778	CDYL	Chromodomain protein on Y chromosome-like	CDYL	9425	ENSG00000153046			Cdyl (MGI:1339956)			
chr6	4992404	5004062	6p25.1	6p25.1		606117	RPP40	"Ribonuclease P, 40kD subunit"	RPP40	10799	ENSG00000124787			Rpp40 (MGI:1346084)			
chr6	5031028	5260949	6p25.1	6p25.1		613311	"LYRM4, ISD11, C6orf149, COXPD19"	LYR motif-containing protein 4	LYRM4	57128	ENSG00000214113	mutation identified in 1 family	"?Combined oxidative phosphorylation deficiency 19, 615595 (3), Autosomal recessive"	Lyrm4 (MGI:2683538)			
chr6	5261000	5771591	6p25.1	6p25.1		611592	"FARS2, FARS1, COXPD14, SPG77"	"Phenylalanyl-tRNA synthetase 2, mitochondrial"	FARS2	10667	ENSG00000145982		"Combined oxidative phosphorylation deficiency 14, 614946 (3), Autosomal recessive; Spastic paraplegia 77, autosomal recessive, 617046 (3), Autosomal recessive"	Fars2 (MGI:1917205)			
chr6	5997998	6007604	6p25.1	6p25.1		607409	"NRN1, NRN"	Neuritin 1	NRN1	51299	ENSG00000124785			Nrn1 (MGI:1915654)			
chr6	6144077	6320690	6p25-p24	6p25.1		134570	"F13A1, F13A"	"Coagulation factor XIII, A polypeptide"	F13A1	2162	ENSG00000124491		"Factor XIIIA deficiency, 613225 (3), Autosomal recessive; {Myocardial infarction, protection against}, 608446 (3); {Venous thrombosis, protection against}, 188050 (3), Autosomal dominant"	F13a1 (MGI:1921395)			
chr6	6588638	6654982	6p25.1	6p25.1		605241	"LY86, MD1"	Lymphocyte antigen 86	LY86	9450	ENSG00000112799			Ly86 (MGI:1321404)			
chr6	7100000	10600000	6p24.3			119530	"OFC1, CL"	Orofacial cleft-1 (cleft lip with or without cleft palate; isolated cleft palate)	OFC1	4963		probable heterogeneity	"Orofacial cleft-1, 119530 (2), Autosomal dominant"				
chr6	7107596	7251979	6p25	6p24.3		602209	RREB1	RAS-responsive element binding protein-1	RREB1	6239	ENSG00000124782			Rreb1 (MGI:2443664)			
chr6	7281142	7313313	6p24.3	6p24.3		600868	SSR1	"Signal sequence receptor, alpha"	SSR1	6745	ENSG00000124783			Ssr1 (MGI:105082)			
chr6	7326653	7389708	6p25.3-p24.1	6p24.3		608304	"CTAG3, CAGE1"	Cancer/testis antigen 3	CAGE1	285782	ENSG00000164304			Cage1 (MGI:1918463)			
chr6	7389828	7418036	6p24.3	6p24.3		617753	"RIOK1, RIO1"	RIO kinase 1	RIOK1	83732	ENSG00000124784			Riok1 (MGI:1918590)			
chr6	7541574	7586716	6p24	6p24.3		125647	"DSP, KPPS2, PPKS2, DCWHKTA"	Desmoplakin	DSP	1832	ENSG00000096696	splice variants result in DP I and DP II	"Arrhythmogenic right ventricular dysplasia 8, 607450 (3), Autosomal dominant; Cardiomyopathy, dilated, with woolly hair and keratoderma, 605676 (3), Autosomal recessive; Dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis, 615821 (3), Autosomal dominant; Epidermolysis bullosa, lethal acantholytic, 609638 (3), Autosomal recessive; Keratosis palmoplantaris striata II, 612908 (3); Skin fragility-woolly hair syndrome, 607655 (3), Autosomal recessive"	Dsp (MGI:109611)			
chr6	7726098	7881727	6p24-p23	6p24.3		112266	BMP6	Bone morphogenetic protein-6	BMP6	654	ENSG00000153162			Bmp6 (MGI:88182)			
chr6	7881513	7910813	6p25.2	6p24.3		616412	"TXNDC5, ERP46, ENDOPDI, HCC2"	Thioredoxin domain-containing protein 5	TXNDC5	81567	ENSG00000239264			Txndc5 (MGI:2145316)			
chr6	8013566	8064413	6p24.3	6p24.3		607289	"BLOC1S5, BLOS5, MUTED"	"Biogenesis of lysosome-related organelles complex 1, subunit 5"	BLOC1S5	63915	ENSG00000188428			Bloc1s5 (MGI:2178598)			
chr6	8073359	8102594	6p25.1-p23	6p24.3		609206	EEF1E1	"Eukaryotic translation elongation factor 1, epsilon-1"	EEF1E1	9521	ENSG00000124802			Eef1e1 (MGI:1913393)			
chr6	8413065	8436168	6p24.3	6p24.3		610845	"SLC35B3, PAPST2"	"Solute carrier family 25 (3'-phosphoadenosine 5'-phosphosulfate transporter), member B3"	SLC35B3	51000	ENSG00000124786			Slc35b3 (MGI:1913978)			
chr6	8652208	8653845	6p24.3	6p24.3		612210	HULC	Highly upregulated in liver cancer	HULC	728655							
chr6	9850415	10211607	6p24	6p24.3		614287	"OFCC1, MRDS1"	OFC1 candidate gene 1	OFCC1	266553				Ofcc1 (MGI:2658851)			
chr6	10396676	10419896	6p24	6p24.3		107580	"TFAP2A, AP2TF, BOFS"	Transcription factor AP-2 alpha (activating enhancer-binding protein 2 alpha)	TFAP2A	7020	ENSG00000137203		"Branchiooculofacial syndrome, 113620 (3), Autosomal dominant"	Tfap2a (MGI:104671)			
chr6	10404501	10407926	6p24.3	6p24.3		617136	HIPSTR	Long noncoding RNA HIPSTR	TFAP2A-AS2	109729173		overlaps TFAP2A					
chr6	10521282	10629367	6p24-p23	6p24.3-p24.2		600429	"GCNT2, Ii, CTRCT13"	"Glucosaminyl (N-acetyl) transferase 2, I-branching enzyme"	GCNT2	2651	ENSG00000111846	previously assigned to 9q21	"Adult i phenotype without cataract, 110800 (3), Autosomal dominant; [Blood group, Ii], 110800 (3), Autosomal dominant; Cataract 13 with adult i phenotype, 116700 (3), Autosomal recessive"	Gcnt2 (MGI:1100870)			
chr6	10690864	10709781	6p24.2	6p24.2		607811	"PAK1IP1, PIP1"	PAK1-interacting protein	PAK1IP1	55003	ENSG00000111845			Pak1ip1 (MGI:1915333)			
chr6	10722914	10731128	6p24.3	6p24.2		615318	TMEM14C	Transmembrane protein 14C	TMEM14C	51522	ENSG00000111843			Tmem14c (MGI:1913404)			
chr6	10762722	10838953	6p24.2	6p24.2		154235	"MAK, RP62"	Male germ cell-associated kinase	MAK	4117	ENSG00000111837		"Retinitis pigmentosa 62, 614181 (3), Autosomal recessive"	Mak (MGI:96913)			
chr6	10873222	10881864	6p24.2	6p24.2		603716	"GCM2, GCMB, HRPT4"	"Glial cells missing, Drosophila, homolog of, 2"	GCM2	9247	ENSG00000124827		"Hyperparathyroidism 4, 617343 (3), Autosomal dominant; Hypoparathyroidism, familial isolated, 146200 (3), Autosomal dominant"	Gcm2 (MGI:1861438)			
chr6	10886830	10974308	6p24.2	6p24.2		616799	"SYCP2L, C6orf177"	Synaptonemal complex protein 2-like	SYCP2L	221711	ENSG00000153157			Sycp2l (MGI:2685114)			
chr6	10980758	11044390	6p24.2	6p24.2		611814	"ELOVL2, SSC2"	Elongation of very long chain fatty acids-like 2	ELOVL2	54898	ENSG00000197977			Elovl2 (MGI:1858960)			
chr6	11102488	11111837	6p24.1	6p24.2		610524	ERVFRD-1	"Endogenous retrovirus group FRD, member 1"	ERVFRD-1	405754	ENSG00000244476			Synb (MGI:3045308)			
chr6	11183297	11382347	6p24.2	6p24.2		602265	"NEDD9, HEF1, CASL"	"Neural precursor cell expressed, developmentally downregulated 9"	NEDD9	4739	ENSG00000111859			Nedd9 (MGI:97302)			
chr6	11600000	25200000	6p24.1-p22.3			607017	DFNA21	"Deafness, autosomal dominant 21"	DFNA21	192644		previously mapped to 6p21.3	"Deafness, autosomal dominant 21, 607017 (2), Autosomal dominant"				
chr6	11713522	11779627	6p24.1	6p24.1		614348	"C6orf105, ADTRP"	Chromosome 6 open reading frame 105 (androgen-dependent TFPI-regulating protein)	ADTRP	84830	ENSG00000111863			Adtrp (MGI:1924596)			
chr6	12002095	12212033	6p24-p22.3	6p24.1		194540	"HIVEP1, ZNF40"	Human immunodeficiency virus type I enhancer-binding protein-1	HIVEP1	3096	ENSG00000095951			Hivep1 (MGI:96100)			
chr6	12256462	12297193	6p24-p23	6p24.1		131240	"EDN1, ARCND3, QME, HDLCQ7"	Endothelin-1	EDN1	1906	ENSG00000078401		"Auriculocondylar syndrome 3, 615706 (3), Autosomal recessive; {High density lipoprotein cholesterol level QTL 7} (3); Question mark ears, isolated, 612798 (3), Autosomal dominant"	Edn1 (MGI:95283)			
chr6	12716634	13290461	6p24.1	6p24.1		608723	"PHACTR1, KIAA1733"	Phosphatase and actin regulator 1	PHACTR1	221692	ENSG00000112137			Phactr1 (MGI:2659021)			
chr6	13304950	13328582	6p24.1	6p24.1		612655	"TBC1D7, PIG51, TBC7, MGCPH"	"TBC1 domain family, member 7"	TBC1D7	51256	ENSG00000145979		"Macrocephaly/megalencephaly syndrome, autosomal recessive, 248000 (3), Autosomal recessive"	Tbc1d7 (MGI:1914296)			
chr6	13400000	15200000	6p23			611456	ETM3	"Tremor, hereditary essential, 3"		101027378		max lod at D6S1630 and D6S1605	"Essential tremor, hereditary, 3, 611456 (2)"				
chr6	13400000	46200000	6p23-p21			271250	"SCAR3, SCABD"	"Spinocerebellar ataxia, autosomal recessive 3"	SCAR3	85502			"Spinocerebellar ataxia, autosomal recessive 3, 271250 (2), Autosomal recessive"				
chr6	13400000	15200000	6p23			600511	SCZD3	"Schizophrenia susceptibility locus, chromosome 6-related"	SCZD3	6365		?same as DTNBP1; cognitive deficit type	"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr6	13574216	13615157	6p23	6p23		604483	SIRT5	"Sirtuin, S. cerevisiae, homolog 5"	SIRT5	23408	ENSG00000124523			Sirt5 (MGI:1915596)			
chr6	13615326	13632469	6p23	6p23		611533	NOL7	Nucleolar protein 7	NOL7	51406	ENSG00000225921			Nol7 (MGI:1917328)			
chr6	13621497	13711581	6p23	6p23		603854	"RANBP9, RANBPM"	RAN-binding protein 9	RANBP9	10048	ENSG00000010017			Ranbp9 (MGI:1928741)			
chr6	13786548	13814993	6p23	6p23		616952	"MCUR1, CCDC90A, FMP32"	Mitochondrial calcium uniporter regulator 1	MCUR1	63933	ENSG00000050393			Mcur1 (MGI:1923387)			
chr6	14117255	14136917	6p23	6p23		604534	"CD83, HB15, BL11"	CD83 antigen	CD83	9308	ENSG00000112149			Cd83 (MGI:1328316)			
chr6	15200000	30500000	6p22			612368	ALPQTL3	"Alkaline phosphatase, plasma level of, QTL 3"		100196915		linkage with rs9467160	"{Alkaline phosphatase, plasma level of, QTL3}, 612368 (2)"				
chr6	15200000	25200000	6p22.3			615192	BWQTL4	Birth weight quantitative trait locus 4		101448071		associated with rs7756992	"[Birth weight QTL4], 615192 (2)"				
chr6	15200000	25200000	6p22.3			613290	CIHL	"Hearing loss, cisplatin-induced, susceptibility to"		100381207		associated with rs12201199	"{?Hearing loss, cisplatin-induced, susceptibility to}, 613290 (2)"				
chr6	15200000	27100000	6p22.3-p22.2			603209	"CMAHP, CMAH"	Cytidine monophospho-N-acetylneuraminic acid hydroxylase pseudogene	CMAHP	8418		mutation inactivates gene in humans					
chr6	15200000	46200000	6p22-p21			600202	DYX2	"Dyslexia, susceptibility to, 2"				?between D6S105 and TNFB	"{Dyslexia, susceptibility to, 2}, 600202 (2), Autosomal dominant"				
chr6	15200000	30500000	6p22			613015	NBLST4	"Neuroblastoma, susceptibility to, 4"		100306937		"associated with rs6939340, rs4712653, rs9295536"	"{Neuroblastoma, susceptibility to, 4}, 613015 (2)"				
chr6	15200000	36600000	6p22.3-p21.3			608244	OTSC3	Otosclerosis 3	OTSC3	170532			"Otosclerosis 3, 608244 (2), Autosomal dominant"				
chr6	15200000	46200000	6p22.3-p21.1			601431	TRNAA1	tRNA alanine-1	TRA-TGC7-1	7154							
chr6	15245974	15522041	6p24-p23	6p22.3		601594	JMJ	Jumonji	JARID2	3720	ENSG00000008083			Jarid2 (MGI:104813)			
chr6	15522800	15663057	6p22.3	6p22.3		607145	"DTNBP1, HPS7"	Dystrobrevin-binding protein 1 (dysbindin)	DTNBP1	84062	ENSG00000047579		"Hermansky-Pudlak syndrome 7, 614076 (3), Autosomal recessive"	Dtnbp1 (MGI:2137586)			
chr6	16129085	16151014	6p23-p22.3	6p22.3		610082	"MYLIP, MIR"	Myosin regulatory light chain-interacting protein	MYLIP	29116	ENSG00000007944			Mylip (MGI:2388271)			
chr6	16238579	16295548	6p23	6p22.3		139265	"GMPR, GMPR1"	Guanosine monophosphate reductase	GMPR	2766	ENSG00000137198			Gmpr (MGI:1913605)			
chr6	16299111	16761489	6p23	6p22.3		601556	"ATXN1, ATX1, SCA1"	Ataxin-1	ATXN1	6310	ENSG00000124788		"Spinocerebellar ataxia 1, 164400 (3), Autosomal dominant"	Atxn1 (MGI:104783)			
chr6	17281507	17293874	6p22.3	6p22.3		617603	"RBM24, RNPC6"	RNA-binding motif protein 24	RBM24	221662	ENSG00000112183			Rbm24 (MGI:3610364)			
chr6	17615034	17706833	6p22.3	6p22.3		603948	NUP153	"Nucleoporin, 153kD"	NUP153	9972	ENSG00000124789			Nup153 (MGI:2385621)			
chr6	17759182	17987622	6p22.3	6p22.3		605433	KIF13A	Kinesin family member 13A	KIF13A	63971	ENSG00000137177			Kif13a (MGI:1098264)			
chr6	18120486	18122619	6p22.3	6p22.3		608072	"NHLRC1, EPM2A, EPM2B"	NHL repeat-containing 1 gene (malin)	NHLRC1	378884	ENSG00000187566		"Epilepsy, progressive myoclonic 2B (Lafora), 254780 (3), Autosomal recessive"	Nhlrc1 (MGI:2145264)			
chr6	18128310	18155168	6p22.3	6p22.3		187680	"TPMT, TPMTD"	Thiopurine S-methyltransferase	TPMT	7172	ENSG00000137364		"{Thiopurines, poor metabolism of, 1}, 610460 (3), Autosomal recessive"	Tpmt (MGI:98812)			
chr6	18155387	18223852	6p22.3	6p22.3		613081	"KDM1B, LSD2, AOF1"	Lysine-specific demethylase 1B	KDM1B	221656	ENSG00000165097						
chr6	18224168	18264567	6p23	6p22.3		125264	"DEK, D6S231E"	DEK oncogene	DEK	7913	ENSG00000124795	fused with CAN in t(6;9)	"Leukemia, acute nonlymphocytic, 125264 (2)"	Dek (MGI:1926209)			
chr6	19837369	19842199	6p22-p21.3	6p22.3		600581	ID4	"Inhibitor of DNA binding 4, dominant negative helix-loop-helix protein"	ID4	3400	ENSG00000172201			Id4 (MGI:99414)			
chr6	20099683	20212463	6p23	6p22.3		611732	MBOAT1	Membrane-bound O-acetyltransferase domain-containing 1	MBOAT1	154141	ENSG00000172197			Mboat1 (MGI:2387184)			
chr6	20401905	20493713	6p22	6p22.3		600427	E2F3	E2F transcription factor 3	E2F3	1871	ENSG00000112242			E2f3 (MGI:1096340)			
chr6	20534456	21232403	6p22.3	6p22.3		611259	CDKAL1	CDK5 regulatory subunit-associated protein 1-like 1	CDKAL1	54901	ENSG00000145996			Cdkal1 (MGI:1921765)			
chr6	21593740	21598618	6p22.3	6p22.3		184430	SOX4	SRY (sex determining region Y)-box 4	SOX4	6659	ENSG00000124766			Sox4 (MGI:98366)			
chr6	21666412	22195819	6p22.3	6p22.3		616610	"CASC15, LINC00340"	"Cancer susceptibility candidate 15, noncoding"	CASC15	401237							
chr6	22134601	22147192	6p22	6p22.3		616206	NBAT1	"Neuroblastoma-associated transcript 1, noncoding"	NBAT1	729177							
chr6	22287243	22302896	6p22.2-p21.3	6p22.3		176760	PRL	Prolactin	PRL	5617	ENSG00000172179	?between 6cen and GLO1		Prl (MGI:97762)			
chr6	24126185	24147528	6p22	6p22.3		616630	"NRSN1, VMP"	Neurensin 1	NRSN1	140767	ENSG00000152954			Nrsn1 (MGI:894662)			
chr6	24171754	24383291	6p22.1	6p22.3		605755	"DCDC2, RU2, KIAA1154, NPHP19, DFNB66, NSC"	Doublecortin domain-containing protein 2	DCDC2	51473	ENSG00000146038	mutation identified in 1 DFNB66 family	"?Deafness, autosomal recessive 66, 610212 (3), Autosomal recessive; Nephronophthisis 19, 616217 (3), Autosomal recessive; Sclerosing cholangitis, neonatal, 617394 (3), Autosomal recessive"	Dcdc2a (MGI:2652818)			
chr6	24356902	24358283	6p22.1	6p22.3		608211	"KAAG1, RU2AS"	Kidney-associated antigen 1	KAAG1	353219	ENSG00000146049						
chr6	24423968	24495231	6p22.1	6p22.3		602515	"GPLD1, PIGPLD, GPIPLD"	"Phospholipase D1, glycosylphosphatidylinositol-specific"	GPLD1	2822	ENSG00000112293			Gpld1 (MGI:106604)			
chr6	24494968	24537206	6p22	6p22.3		610045	"ALDH5A1, SSADH"	Succinic semialdehyde dehydrogenase	ALDH5A1	7915	ENSG00000112294		"Succinic semialdehyde dehydrogenase deficiency, 271980 (3), Autosomal recessive"	Aldh5a1 (MGI:2441982)			
chr6	24540127	24646154	6p22.2	6p22.3		609269	KIAA0319	KIAA0319 gene	KIAA0319	9856	ENSG00000137261			D130043K22Rik (MGI:3036268)			
chr6	24649976	24666886	6p22.3-p22.1	6p22.3		605764	"TDP2, TTRAP"	Tyrosyl-DNA phosphodiesterase 2	TDP2	51567	ENSG00000111802		"Spinocerebellar ataxia, autosomal recessive 23, 616949 (3), Autosomal recessive"	Tdp2 (MGI:1860486)			
chr6	24667034	24705068	6p22.3	6p22.3		615652	"ACOT13, THEM2"	Acyl-CoA thioesterase 13	ACOT13	55856	ENSG00000112304			Acot13 (MGI:1914084)			
chr6	24774930	24786098	6p22.3	6p22.3		602842	"GMNN, MGORS6"	Geminin	GMNN	51053	ENSG00000112312		"Meier-Gorlin syndrome 6, 616835 (3), Autosomal dominant"	Gmnn (MGI:1927344)			
chr6	24804280	25042287	6p22.3-p21.32	6p22.3		611410	"FAM65B, C6orf32, KIAA0386, PL48, DFNB104"	"Family with sequence similarity 65, member B"	RIPOR2	9750	ENSG00000111913	mutation identified in 1 DFNB104 family	"?Deafness, autosomal recessive 104, 616515 (3), Autosomal recessive"	Ripor2 (MGI:2444879)			
chr6	25279427	25620529	6p22.2	6p22.2		609593	"LRRC16A, LRRC16, CARMIL"	Leucine-rich repeat-containing protein 16A	CARMIL1	55604	ENSG00000079691			Carmil1 (MGI:1915982)			
chr6	25723742	25832107	6p23-p21.3	6p22.2		182308	"SLC17A1, NPT1"	"Solute carrier family 17, sodium phosphate, member-1 (Sodium phosphate transport 1, kidney)"	SLC17A1	6568	ENSG00000124568			Slc17a1 (MGI:103209)			
chr6	25726062	25726561	6p22.2	6p22.2		613499	"HISTH2AA, H2AFR, H2AA"	"Histone gene cluster 1, H2A histone family, member A"	HIST1H2AA	221613	ENSG00000164508			Hist1h2ak (MGI:2448297)			
chr6	25726908	25727344	6p22.2	6p22.2		609904	"HIST1H2BA, TSH2B"	"Histone 1, H2BA"	HIST1H2BA	255626	ENSG00000146047			Hist1h2ba (MGI:2448375)			
chr6	25754672	25781174	6p22-p21.3	6p22.2		604216	SLC17A4	"Solute carrier family 17 (sodium phosphate), member 4"	SLC17A4	10050	ENSG00000146039			Slc17a4 (MGI:2442850)			
chr6	25845099	25874242	6p21.3	6p22.2		611034	"SLC17A3, NPT4, UAQTL4, GOUT4"	"Solute carrier family 17 (sodium phosphate cotransporter), member 3"	SLC17A3	10786	ENSG00000124564		"{Gout susceptibility 4}, 612671 (3), Autosomal dominant; [Uric acid concentration, serum, QTL4], 612671 (3), Autosomal dominant"	Slc17a3 (MGI:2389216)			
chr6	25912753	25930726	6p21.3	6p22.2		611049	"SLC17A2, NPT3"	"Solute carrier family 17 (sodium phosphate cotransporter), member 2"	SLC17A2	10246	ENSG00000112337			Slc17a2 (MGI:2443098)			
chr6	26017031	26017811	6p21.3	6p22.2		142709	"HIST1H1A, H1F1"	"Histone 1, H1a"	HIST1H1A	3024	ENSG00000124610						
chr6	26020489	26020957	6p21.3	6p22.2		602810	"HIST1H3A, H3FA"	"Histone 1, H3a"	HIST1H3A	8350	ENSG00000275714			Hist1h3d (MGI:2448322)			
chr6	26021678	26022049	6p21.3	6p22.2		602822	"HIST1H4A, H4FA"	"Histone 1, H4a"	HIST1H4A	8359	ENSG00000278637			Hist1h4d (MGI:2448423)			
chr6	26026895	26027251	6p21.3	6p22.2		602829	"HIST1H4B, H4FI"	"Histone 1, H4b"	HIST1H4B	8366	ENSG00000278705			Hist4h4 (MGI:2448443)			
chr6	26031588	26032059	6p21.3	6p22.2		602819	"HIST1H3B, H3FL"	"Histone 1, H3fl"	HIST1H3B	8358	ENSG00000274267	in major cluster on 6p		Hist2h3b (MGI:2448351)			
chr6	26033091	26033567	6p21.3	6p22.2		602795	"HIST1H2AB, H2AFM"	"Histone 1, H2ab"	HIST1H2AB	8335	ENSG00000278463			Hist1h2ag (MGI:2448293)			
chr6	26043226	26043656	6p21.3	6p22.2		602803	"HIST1H2BB, H2BFF"	"Histone 1, H2bb"	HIST1H2BB	3018	ENSG00000276410			Hist1h2bb (MGI:2448377)			
chr6	26045410	26045868	6p21.3	6p22.2		602812	"HIST1H3C, H3FC"	"Histone 1, H3c"	HIST1H3C	8352	ENSG00000278272			Hist2h3c1 (MGI:2448355)			
chr6	26055739	26056470	6p21.3	6p22.2		142710	"HIST1H1C, H1F2"	"Histone 1, H1c"	HIST1H1C	3006	ENSG00000187837			Hist1h1c (MGI:1931526)			
chr6	26087280	26096215	6p21.3	6p22.2		613609	"HFE, HLA-H, HFE1, MVCD7, TFQTL2"	Hemochromatosis gene	HFE	3077	ENSG00000010704		"{Alzheimer disease, susceptibility to}, 104300 (3), Autosomal dominant; Hemochromatosis, 235200 (3), Autosomal recessive; {Microvascular complications of diabetes 7}, 612635 (3); {Porphyria cutanea tarda, susceptibility to}, 176100 (3), Autosomal recessive, Autosomal dominant; {Porphyria variegata, susceptibility to}, 176200 (3), Autosomal dominant; [Transferrin serum level QTL2], 614193 (3)"	Hfe (MGI:109191)			
chr6	26103947	26104336	6p21.3	6p22.2		602827	"HIST1H4C, H4FG"	"Histone 1, H4c"	HIST1H4C	8364	ENSG00000197061			Hist2h4 (MGI:2140113)			
chr6	26107411	26108135	6p21.3	6p22.2		142712	"HIST1H1T, H1FT"	"Histone 1, H1t"	HIST1H1T	3010	ENSG00000187475			Hist1h1t (MGI:1888530)			
chr6	26123466	26123903	6p21.3	6p22.2		602847	"HIST1H2BC, H2BFL"	"Histone 1, H2bc"	HIST1H2BC	8347	ENSG00000180596			Hist1h2bg (MGI:2448386)			
chr6	26124144	26124689	6p21.3	6p22.2		602794	"HIST1H2AC, H2AFL"	"Histone 1, H2ac"	HIST1H2AC	8334	ENSG00000180573			Hist1h2ao (MGI:2448302)			
chr6	26156330	26157114	6p21.3	6p22.2		142220	"HIST1H1E, H1F4, RMNS"	"Histone 1, H1e"	HIST1H1E	3008	ENSG00000168298		"Rahman syndrome, 617537 (3), Autosomal dominant"				
chr6	26158007	26171348	6p21.3	6p22.2		602799	"HIST1H2BD, H2BFB"	"Histone 1, H2bd"	HIST1H2BD	3017	ENSG00000158373			Hist3h2ba (MGI:1925553)			
chr6	26183795	26184229	6p21.3	6p22.2		602805	"HIST1H2BE, H2BFH"	"Histone 1, H2be"	HIST1H2BE	8344	ENSG00000274290			Hist1h2bl (MGI:2448403)			
chr6	26188709	26189075	6p21.3	6p22.2		602823	"HIST1H4D, H4FB"	"Histone 1, H4d"	HIST1H4D	8360	ENSG00000277157			Hist1h4m (MGI:2448441)			
chr6	26196783	26199292	6p21.3	6p22.2		602811	"HIST1H3D, H3FB"	"Histone 1, H3d"	HIST1H3D	8351	ENSG00000197409			Hist1h3a (MGI:2668828)			
chr6	26198783	26199292	6p21.3	6p22.2		602792	"HIST1H2AD, H2AFG"	"Histone 1, H2ad"	HIST1H2AD	3013	ENSG00000196866			Hist1h2ab (MGI:2448306)			
chr6	26199558	26199987	6p21.3	6p22.2		602804	"HIST1H2BF, H2BFG"	"Histone 1, H2bf"	HIST1H2BF	8343	ENSG00000277224			Hist1h2be (MGI:2448380)			
chr6	26204644	26205020	6p21.3	6p22.2		602830	"HIST1H4E, H4FJ"	"Histone 1, H4e"	HIST1H4E	8367	ENSG00000276966						
chr6	26216199	26216643	6p21.3	6p22.2		602798	"HIST1H2BG, H2BFA"	"Histone 1, H2bg"	HIST1H2BG	8339	ENSG00000273802			Hist1h2bf (MGI:2448383)			
chr6	26216919	26217482	6p21.3	6p22.2		602786	"HIST1H2AE, H2AFA"	"Histone 1, H2ae"	HIST1H2AE	3012	ENSG00000277075			Hist1h2ai (MGI:2448457)			
chr6	26225154	26225615	6p21.3	6p22.2		602813	"HIST1H3E, H3FD, H3.1"	"Histone 1, H3e"	HIST1H3E	8353	ENSG00000274750	in cluster of 35 histone genes		Hist1h3h (MGI:2448349)			
chr6	26234211	26234987	6p21.3	6p22.2		142210	"HIST1H1D, H1F3"	"Histone 1, H1d"	HIST1H1D	3007	ENSG00000124575			Hist1h1d (MGI:107502)			
chr6	26240425	26240792	6p21.3	6p22.2		602824	"HIST1H4F, H4FC"	"Histone 1, H4f"	HIST1H4F	8361	ENSG00000274618			Hist1h4c (MGI:2448421)			
chr6	26246610	26246976	6p21.3	6p22.2		602832	"HIST1H4G, H4FL"	"Histone 1, H4g"	HIST1H4G	8369	ENSG00000275663						
chr6	26250141	26250606	6p21.3	6p22.2		602816	HIST1H3F	"Histone 1, H3f"	HIST1H3F	8968	ENSG00000277775			Hist1h3i (MGI:2448350)			
chr6	26251650	26252074	6p21.3	6p22.2		602806	"HIST1H2BH, H2BFJ"	"Histone 1, H2bh"	HIST1H2BH	8345	ENSG00000275713			"Hist1h2br,Hist1h2bq (MGI:3710645,MGI:3702051)"			
chr6	26270917	26271383	6p21.3	6p22.2		602815	"HIST1H3G, H3FH"	"Histone 1, H3g"	HIST1H3G	8355	ENSG00000273983			Hist2h3c2 (MGI:2448357)			
chr6	26272975	26273411	6p21.3	6p22.2		602807	"HIST1H2BI, H2BFK"	"Histone 1, H2bi"	HIST1H2BI	8346	ENSG00000278588			Hist1h2bc (MGI:1915274)			
chr6	26285125	26285498	6p21.3	6p22.2		602828	"HIST1H4H, H4FH"	"Histone 1, H4h"	HIST1H4H	8365	ENSG00000158406			Hist1h4k (MGI:2448439)			
chr6	26286525	26286596	6p23-q12	6p22.2		180621	"TRNAM1, TRMI2, TRM2, RNTMT1"	tRNA methionine-1	TRX-CAT1-2	7210							
chr6	26299676	26299748	6p22.3-p21.1	6p22.2		601432	"TRNAR3, TRR3"	tRNA arginine-3	TRR-TCG4-1	7232							
chr6	26365158	26378319	6p22.1	6p22.2		613594	"BTN3A2, BTF4"	"Butyrophilin, subfamily 3, member A2"	BTN3A2	11118	ENSG00000186470						
chr6	26382892	26394873	6p22.1	6p22.2		613591	"BTN2A2, BTF2"	"Butyrophilin, subfamily 2, member A2"	BTN2A2	10385	ENSG00000124508			Btn2a2 (MGI:3606486)			
chr6	26402236	26415215	6p22.1	6p22.2		613593	"BTN3A1, BTF5, CD277"	"Butyrophilin, subfamily 3, member A1"	BTN3A1	11119	ENSG00000026950						
chr6	26421390	26430587	6p22.1	6p22.2		613592	BTN2A3	"Butyrophilin, subfamily 2, member A3"	BTN2A3P	54718							
chr6	26440471	26453414	6p22.1	6p22.2		613595	"BTN3A3, BTF3"	"Butyrophilin, subfamily 3, member A3"	BTN3A3	10384	ENSG00000111801						
chr6	26457903	26476620	6p22.1	6p22.2		613590	"BTN2A1, BTF1"	"Butyrophilin, subfamily 2, member A1"	BTN2A1	11120	ENSG00000112763						
chr6	26499289	26510424	6p22.1	6p22.2		601610	"BTN1A1, BTN"	Butyrophilin	BTN1A1	696	ENSG00000124557			Btn1a1 (MGI:103118)			
chr6	26537497	26537569	6p22.2	6p22.2		615305	TRNAR2	Transfer RNA arginine 2	TRR-ACG1-2	7231							
chr6	26538053	26538125	6p22.2	6p22.2		615306	TRNAV21	Transfer RNA valine 21	TRV-CAC1-6	100189227							
chr6	26634382	26659751	6p22.1	6p22.2		610847	"ZNF322A, ZNF489, ZNF322"	Zinc finger protein 322A	ZNF322	79692	ENSG00000181315			Zfp322a (MGI:2442566)			
chr6	27100000	30500000	6p22.1			612892	STQTL18	Stature quantitative trait locus 18		100302683		associated with rs10946808	"{Stature QTL 18}, 612892 (2)"				
chr6	27132315	27132795	6p22-p21.3	6p22.1		615044	"HIST1H2BJ, H2BJ"	"Histone gene cluster 1, H2B histone family, member J"	HIST1H2BJ	8970	ENSG00000124635			Hist2h2be (MGI:2448415)			
chr6	27133037	27133534	6p22-p21.3	6p22.1		615012	"HIST1H2AG, H2AG, H2AFP"	"Histone gene cluster 1, H2A histone family, member 6"	HIST1H2AG	8969	ENSG00000196787			Hist1h2an (MGI:2448300)			
chr6	27138292	27146857	6p22-p21.3	6p22.1		615045	"HIST1H2BK, H2BK"	"Histone gene cluster 1, H2B histone family, member K"	HIST1H2BK	85236	ENSG00000197903			Hist1h2bk (MGI:2448399)			
chr6	27139308	27139677	6p21.3	6p22.1		602833	"HIST1H4I, H4FM, H4M"	"Histone 1, H4i"	HIST1H4I	8294	ENSG00000276180			Hist1h4h (MGI:2448427)			
chr6	27147081	27147561	6p22-p21.3	6p22.1		615013	"HIST1H2AH, H2AH"	"Histone gene cluster 1, H2A histone family, member H"	HIST1H2AH	85235	ENSG00000274997			Hist1h2ah (MGI:2448295)			
chr6	27235508	27235580	6p22.1	6p22.1		615307	TRNAV12	Transfer RNA valine 12	TRV-AAC5-1	100189014							
chr6	27247700	27256619	6p22-p21.3	6p22.1		607169	"PRSS16, TSSP"	"Protease, serine, 16"	PRSS16	10279	ENSG00000112812			Prss16 (MGI:1859181)			
chr6	27404009	27473117	6p21.3	6p22.1		602277	ZNF184	Zinc finger protein-184	ZNF184	7738	ENSG00000096654			Zfp184 (MGI:1922244)			
chr6	27495813	27495894	6p22.1	6p22.1		189910	"TRS-AGA2-4, TRNAS2, TRS2, TRNS"	Transfer RNA serine (AGA) 2-4	TRS-AGA2-3	23437							
chr6	27505827	27505908	6p22.1	6p22.1		606172	"TRS-TGA4-1, TRNAS3, TRS3"	Transfer RNA serine (TGA) 4-1	TRS-TGA4-1	23540							
chr6	27681105	27681177	6p22.1	6p22.1		615308	TRNAV17	Transfer RNA valine 17	TRV-AAC4-1	100189161							
chr6	27684694	27684767	6p22.1	6p22.1		615309	TRNAT15	Transfer RNA threonine 15	TRT-AGT2-2	100189340							
chr6	27777884	27777955	6p23-q12	6p22.1		180620	"TRNAM2, TRNAMI2, RNTMI2"	tRNA methionine-2	TRX-CAT2-1	7212		2 of 12+ RNTMI genes are on chr. 6					
chr6	27807478	27807930	6p22-p21.3	6p22.1		602800	"HIST1H2BL, H2BFC"	"Histone 1, H2bl"	HIST1H2BL	8340	ENSG00000185130			Hist1h2bj (MGI:2448388)			
chr6	27808198	27808666	6p22-p21.3	6p22.1		602787	"HIST1H2AI, H2AFC"	"Histone 1, H2ai"	HIST1H2AI	8329	ENSG00000196747						
chr6	27810063	27810535	6p22-p21.3	6p22.1		602818	"HIST1H3H, H3FK"	"Histone 1, H3h"	HIST1H3H	8357	ENSG00000278828	in minor cluster on 6p		Hist1h3b (MGI:2448319)			
chr6	27814301	27814739	6p22-p21.3	6p22.1		602791	"HIST1H2AJ, HIST1H2AK, H2AFE"	"Histone 1, H2aj"	HIST1H2AJ	8331	ENSG00000276368			Hist1h2af (MGI:2448309)			
chr6	27815043	27815488	6p22-p21.3	6p22.1		602802	"HIST1H2BM, H2BFE"	"Histone 1, H2bm"	HIST1H2BM	8342	ENSG00000273703			Hist1h2bn (MGI:2448407)			
chr6	27824124	27824479	6p22-p21.3	6p22.1		602826	"HIST1H4J, H4FE"	"Histone 1, H4j"	HIST1H4J	8363	ENSG00000197238			Hist1h4f (MGI:2448425)			
chr6	27831173	27831526	6p22-p21.3	6p22.1		602825	"HIST1H4K, H4FD"	"Histone 1, H4k"	HIST1H4K	8362	ENSG00000273542			Hist1h4j (MGI:2448436)			
chr6	27837879	27838338	6p22-p21.3	6p22.1		602788	"HIST1H2AK, HIST1H2AI, H2AFD"	"Histone 1, H2ak"	HIST1H2AK	8330	ENSG00000275221			Hist1h2ac (MGI:2448287)			
chr6	27838661	27839109	6p22-p21.3	6p22.1		602801	"HIST1H2BN, H2BFD"	"Histone 1, H2bn"	HIST1H2BN	8341	ENSG00000233822			Hist1h2bm (MGI:2448404)			
chr6	27865328	27865797	6p22-p21.3	6p22.1		602793	"HIST1H2AL, H2AFI"	"Histone 1, H2al"	HIST1H2AL	8332	ENSG00000276903			Hist1h2ae (MGI:2448290)			
chr6	27866791	27867580	6p22-p21.3	6p22.1		142711	"HIST1H1B, H1F5"	"Histone 1, H1b"	HIST1H1B	3009	ENSG00000184357	~2Mb centromeric of H1F1 cluster					
chr6	27871844	27872320	6p22-p21.3	6p22.1		602814	"HIST1H3I, H3FF"	"Histone 1, H3i"	HIST1H3I	8354	ENSG00000275379	in cluster of 16 histone genes centromeric of major cluster		Hist1h3e (MGI:2448326)			
chr6	27873147	27873510	6p22-p21.3	6p22.1		602831	"HIST1H4L, H4FK"	"Histone 1, H4l"	HIST1H4L	8368	ENSG00000275126			Hist1h4n (MGI:4843992)			
chr6	27890314	27890791	6p22-p21.3	6p22.1		602817	"HIST1H3J, H3FJ"	"Histone 1, H3j"	HIST1H3J	8356	ENSG00000197153	in 2nd cluster on 6p		Hist1h3g (MGI:2145541)			
chr6	27892698	27893184	6p22-p21.3	6p22.1		602796	"HIST1H2AM, H2AFN"	"Histone 1, H2am"	HIST1H2AM	8336	ENSG00000278677			Hist1h2ad (MGI:2448289)			
chr6	27893424	27893890	6p22-p21.3	6p22.1		602808	"HIST1H2BO, H2BFN"	"Histone 1, H2bo"	HIST1H2BO	8348	ENSG00000274641			Hist1h2bp (MGI:2448409)			
chr6	28080703	28104243	6p21.3	6p22.1		600834	"ZNF165, LD65"	Zinc finger protein-165	ZNF165	7718	ENSG00000197279						
chr6	28141642	28159471	6p21.3	6p22.1		602240	ZNF192	Zinc finger protein-192	ZKSCAN8	7745	ENSG00000198315			Zkscan8 (MGI:1913815)			
chr6	28224701	28233486	6p21.3	6p22.1		602246	ZNF193	Zinc finger protein-193	ZSCAN9	7746	ENSG00000137185						
chr6	28241696	28259257	6p21.33-p21.31	6p22.1		611643	"ZKSCAN4, ZNF307"	Zinc finger with KRAB and SCAN domains 4	ZKSCAN4	387032	ENSG00000187626						
chr6	28267009	28278223	6p22.1	6p22.1		616474	"ZSCAN26, SREZBP"	Zinc finger- and SCAN domain-containing protein 26	ZSCAN26	7741	ENSG00000197062			Zscan26 (MGI:3531417)			
chr6	28324736	28359156	6p22.3-p22.1	6p22.1		610794	ZNF323	Zinc finger protein 323	ZSCAN31	64288	ENSG00000235109						
chr6	28349912	28369176	6p22.1	6p22.1		612791	"ZKSCAN3, ZNF306"	Zinc finger protein with KRAB and SCAN domains 3	ZKSCAN3	80317	ENSG00000189298			Zkscan3 (MGI:1919989)			
chr6	28378820	28399767	6p22.2-p21.3	6p22.1		603978	"ZSCAN12, ZNF96, KIAA0426"	Zinc finger- and SCAN domain-containing protein 12	ZSCAN12	9753	ENSG00000158691			Zscan12 (MGI:1099444)			
chr6	28503295	28515792	6p22.1	6p22.1		607913	GPX6	Glutathione peroxidase 6	GPX6	257202	ENSG00000198704			Gpx6 (MGI:1922762)			
chr6	28526011	28534950	6p22.1	6p22.1		603435	GPX5	Glutathione peroxidase 5 (epididymal)	GPX5	2880	ENSG00000224586			Gpx5 (MGI:104886)			
chr6	28568287	28616176	6p22.1	6p22.1		615254	"SCAND3, ZBED9, BUSTER4, KIAA1925"	SCAN domain-containing protein 3	ZBED9	114821	ENSG00000232040						
chr6	28903001	28923990	6p22	6p22.1		602165	"TRIM27, RFP"	Tripartite motif-containing 27	TRIM27	5987	ENSG00000204713			Trim27 (MGI:97904)			
chr6	29111809	29112883	6p22.1	6p22.1		615016	"OR2J3, C3HEXS"	"Olfactory receptor, family 2, subfamily J, member 3"	OR2J3	442186	ENSG00000204701		"[C3HEX, ability to smell], 615082 (3), Autosomal dominant"				
chr6	29486696	29487955	6p21	6p22.1		607235	"MAS1L, MRG"	MAS1 oncogene-like	MAS1L	116511	ENSG00000204687						
chr6	29555611	29559924	6p21.3	6p22.1		606050	"UBD, FAT10"	Ubiquitin D	UBD	10537	ENSG00000213886			Ubd (MGI:1344410)			
chr6	29586523	29592505	6p21.3	6p22.1		600578	"OR2H3, OLFR2"	"Olfactory receptor, family 2, subfamily H, member 3 (olfactory receptor 2)"	OR2H2	7932	ENSG00000204657	in class I MHC region		Olfr90 (MGI:2177473)			
chr6	29602227	29633134	6p21.3	6p22.1		603540	"GABBR1, GABABR1"	Gamma-aminobutyric acid B receptor 1	GABBR1	2550	ENSG00000204681			Gabbr1 (MGI:1860139)			
chr6	29656980	29672371	6p21.3	6p22.1		159465	"MOG, NRCLP7"	Myelin-oligodendrocyte glycoprotein	MOG	4340	ENSG00000204655	60kb telomeric to HLA-F; mutation identified in 1 NRCLP7 family	"?Narcolepsy 7, 614250 (3), Autosomal dominant"	Mog (MGI:97435)			
chr6	29672391	29681149	6p22.1	6p22.1		612192	"ZFP57, TNDM1"	"Zinc finger protein 57, mouse, homolog of"	ZFP57	346171	ENSG00000204644		"Diabetes mellitus, transient neonatal, 1, 601410 (3)"	Zfp57 (MGI:99204)			
chr6	29723339	29740354	6p21.3	6p22.1		143110	"HLA-F, HLA-CDA12, HLAF"	"Major histocompatibility complex, class I, F"	HLA-F	3134	ENSG00000204642			"Gm11127,Gm7030 (MGI:3779381,MGI:3647514)"			
chr6	29826966	29831129	6p21.3	6p22.1		142871	HLA-G	"HLA-G histocompatibility antigen, class I"	HLA-G	3135	ENSG00000204632		"{Asthma, susceptibility to}, 600807 (2), Autosomal dominant"	H2-M3 (MGI:95915)			
chr6	29942469	29945883	6p21.3	6p22.1		142800	HLA-A	"Major histocompatibility complex, class I, A"	HLA-A	3105	ENSG00000206503		"{Hypersensitivity syndrome, carbamazepine-induced, susceptibility to}, 608579 (3)"	"Gm8909,H2-Bl,H2-Q6,H2-K1,H2-Q7,H2-Q4,H2-Q2,Gm10499,H2-Q1,H2-D1,H2-Q10 (MGI:95935,MGI:95936,MGI:95904,MGI:3702919,MGI:95931,MGI:892004,MGI:95933,MGI:3704134,MGI:95896,MGI:95928,MGI:95929)"			
chr6	29975114	29978402	6p21.3	6p22.1		615797	"HCG9, HCGIX, HCGIX4"	"HLA complex group 9, noncoding"	HCG9	10255							
chr6	30001010	30061188	6p22.1	6p22.1		615714	"ZNRD1AS1, TCTEX4, HTEX4"	ZNRD1 antisense RNA 1	ZNRD1ASP	80862							
chr6	30061239	30064908	6p22.1	6p22.1		607525	"ZNRD1, TCTEX6, HTEX6"	Zinc ribbon domain-containing protein 1	ZNRD1	30834	ENSG00000066379			Znrd1 (MGI:1913386)			
chr6	30066863	30070332	6p21.3	6p22.1		606670	"PPP1R11, TCTEX5"	"Protein phosphatase 1, regulatory subunit 11"	PPP1R11	6992	ENSG00000204619			Ppp1r11 (MGI:1923747)			
chr6	30070265	30080624	6p21.3	6p22.1		607524	"RNF39, HZFW, HZF, LIRF"	Ring finger protein 39	RNF39	80352	ENSG00000204618			Rnf39 (MGI:2156378)			
chr6	30102891	30113105	6p23-p21	6p22.1		609316	"TRIM31, HCGI"	Tripartite motif-containing protein 31	TRIM31	11074	ENSG00000204616			Trim31 (MGI:2385051)			
chr6	30135997	30148772	6p22.1	6p22.1		616976	"TRIM40, RNF35"	Tripartite motif-containing protein 40	TRIM40	135644	ENSG00000204614			Trim40 (MGI:2684881)			
chr6	30151938	30163215	6p21.3	6p22.1		605701	"RNF9, RFB30, HERF1"	RING finger protein-9	TRIM10	10107	ENSG00000204613			Trim10 (MGI:1338757)			
chr6	30184452	30213493	6p21.3	6p22.1		600830	ZNF173	Zinc finger protein-173	TRIM26	7726	ENSG00000234127			Trim26 (MGI:1337056)			
chr6	30326843	30343728	6p22.1-p21.3	6p22.1		605700	"TRIM39, RNF23, TFP"	Tripartite motif-containing 39	TRIM39	56658	ENSG00000204599			Trim39 (MGI:1890659)			
chr6	30345128	30346857	6p21	6p22.1		612524	RPP21	"Ribonuclease P/MRP, 21kD subunit"	RPP21	79897	ENSG00000241370			Rpp21 (MGI:1914926)			
chr6	30489405	30494204	6p21.3	6p22.1		143010	HLA-E	"Major histocompatibility complex, class I, E"	HLA-E	3133	ENSG00000204592			"H2-T23,H2-T-ps (MGI:95957,MGI:2442805)"			
chr6	30500000	36600000	6p21.3			107320	ATPLS	"Antiphospholipid syndrome, familial"		100499532		possible linkage with HLA-DRB1*14	"?Antiphospholipid syndrome, familial, 107320 (2), Autosomal dominant"				
chr6	30500000	40500000	6p21.3-p21.2			153380	CP20	"Lymphocyte cytosolic protein, molecular weight 20kD"		7938							
chr6	30500000	36600000	6p21.3			612862	CTEPH1	"Pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to"		100302516		associated with DPB1*0202	"{Pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to}, 612862 (2)"				
chr6	30500000	36600000	6p21.3			608645	DFNA31	"Deafness, autosomal dominant 31"	DFNA31	347737		between D6S276 and D6S273	"Deafness, autosomal dominant 31, 608645 (2), Autosomal dominant"				
chr6	30500000	46200000	6p21			608816	EJM3	"Epilepsy, juvenile myoclonic 3"		449018			"Epilepsy, juvenile myoclonic 3, 608816 (2)"				
chr6	30500000	32100000	6p21.33			613024	FL1	"Follicular lymphoma, susceptibility to, 1"		100306940		associated with rs6457327	"{Follicular lymphoma, susceptibility to, 1}, 613024 (2)"				
chr6	30500000	36600000	6p21.3			615801	"HCG8, HCGVIII"	HLA complex group 8									
chr6	30500000	36600000	6p21.3			612735	"HLA-DRB3, HLA-DR52"	"Major histocompatibility complex, class II, DR beta-3"	HLA-DRB3	3125							
chr6	30500000	36600000	6p21.3			604519	IBD3	Inflammatory bowel disease 3	IBD3	30829			"{Inflammatory bowel disease 3}, 604519 (2), Autosomal dominant"				
chr6	30500000	36600000	6p21.3			222100	IDDM1	Insulin-dependent diabetes mellitus-1				"linkage or association, with HLA"	"{Diabetes mellitus, insulin-dependent-1}, 222100 (2), Autosomal recessive"				
chr6	30500000	36600000	6p21.3			137100	IGAD1	Immunoglobulin A deficiency	IGAD1	10986			"Immunoglobulin A deficiency, 137100 (2), Autosomal recessive, Autosomal dominant, Isolated cases"				
chr6	30500000	36600000	6p21.3			146820	IGAT	Immune response to synthetic polypeptide--IRGAT		7927		in B/D segment					
chr6	30500000	36600000	6p21.3			147080	IGLP1	Immune response to synthetic polypeptides-1	IGLP1	7925							
chr6	30500000	36600000	6p21.3			147090	IGLP2	Immune response to synthetic polypeptides-2	IGLP2	7926							
chr6	30500000	36600000	6p21.3			146850	ISCW	Immune suppression to streptococcal antigen		7928		HLA-linked					
chr6	30500000	40500000	6p21.3-p21.2			150270	LAP	Laryngeal adductor paralysis		7939		?linkage to HLA and GLO1	"?Laryngeal adductor paralysis, 150270 (2), Autosomal dominant"				
chr6	30500000	46200000	6p21			601086	LATD	"Laterality defects, autosomal dominant"		207115		max lod 2.95 at theta = 0					
chr6	30500000	32100000	6p21.33			612593	LNCR4	Lung cancer susceptibility 4		100271693		associated with rs3117582 and rs3131379	"{Lung cancer susceptibility 4}, 612593 (2)"				
chr6	30500000	36600000	6p21.3			614692	MBNP	"Membranous nephropathy, susceptibility to"		101154649			"{?Membranous nephropathy, susceptibility to}, 614692 (2)"				
chr6	30500000	40500000	6p21.3-p21.2			614644	MPVQTL4	Mean platelet volume quantitative trait locus 4		100887753		associated with rs210134	"Mean platelet volume QTL4, 614644 (2)"				
chr6	30500000	36600000	6p21.3			607085	MYAS1	Myasthenia gravis with thymus hyperplasia		246750			"Myasthenia gravis with thymus hyperplasia, 607085 (2)"				
chr6	30500000	36600000	6p21.3			272370	"NKS1, EC1"	Susceptibility to lysis by alloreactive natural killer cells	NKS1	4819							
chr6	30500000	36600000	6p21.3			161550	NPCA2	"Nasopharyngeal carcinoma, susceptibility to, 2"		100312951		associated with rs2517713 and rs2975042	"{Nasopharyngeal carcinoma, susceptibility to, 2}, 161550 (2)"				
chr6	30500000	36600000	6p21.3			613007	PBC2	"Biliary cirrhosis, primary, 2"		100303716		associated with rs2856683	"{Biliary cirrhosis, primary, 2}, 613007 (2)"				
chr6	30500000	36600000	6p21.3			600089	PBCA	"Pancreatic beta cell, agenesis of"		7962		uniparental disomy	"?Diabetes mellitus, insulin-dependent, neonatal, 600089 (2), Autosomal recessive"				
chr6	30500000	36600000	6p21.3			604809	PBLT	"Panbronchiolitis, diffuse"					"Panbronchiolitis, diffuse, 604809 (2), Multifactorial"				
chr6	30500000	36600000	6p21.3			614590	PDCOS	"Podoconiosis, susceptibility to"		100885774			"{Podoconiosis, susceptibility to}, 614590 (2)"				
chr6	30500000	46200000	6p21			611185	RLS6	"Restless legs syndrome, susceptibility to, 6"		100302512		associated with rs9296249 and rs9357271	"{Restless legs syndrome 6}, 611185 (2)"				
chr6	30500000	36600000	6p21.3			179450	RWS	Ragweed sensitivity		7937		"?linkage or association, with HLA"	"?Ragweed sensitivity, 179450 (2), Autosomal dominant"				
chr6	30500000	36600000	6p21.3			193200	VAMAS6	Vitiligo-associated multiple autoimmune disease susceptibility 6		246319		possible second locus on 1p31.3-p32.2	"{Vitiligo-associated multiple autoimmune disease susceptibility 6}, 193200 (2), Autosomal recessive"				
chr6	30500000	36600000	6p21.3			608710	WG	Wegener granulomatosis		474168			"Wegener granulomatosis, 608710 (2)"				
chr6	30500000	36600000	6p21.3			153600	WM1	"Macroglobulinemia, Waldenstrom, susceptibility to, 1"		100188787		linked to HLA	"{Macroglobulinemia, Waldenstrom, susceptibility to, 1}, 153600 (2), Autosomal dominant"				
chr6	30500000	36600000	6p21.3			603282	ZNF204	Zinc finger protein-204	ZNF204P	7754		?pseudogene					
chr6	30541376	30557593	6p21.3	6p21.33		143024	"GNL1, HSR1"	Guanine nucleotide-binding protein-like 1	GNL1	2794	ENSG00000204590			Gnl1 (MGI:95764)			
chr6	30571392	30591531	6p21.33	6p21.33		603429	"ABCF1, ABC50"	"ATP-binding cassette 50, TNF-alpha stimulated"	ABCF1	23	ENSG00000204574			Abcf1 (MGI:1351658)			
chr6	30584331	30584416	6p21.33	6p21.33		611619	"MIR877, MIRN877"	Micro RNA 877	MIR877	100126314							
chr6	30600399	30618606	6p21.3	6p21.33		603771	"PPP1R10, PNUTS"	"Protein phosphatase 1, regulatory subunit 10"	PPP1R10	5514	ENSG00000204569			Ppp1r10 (MGI:1289273)			
chr6	30617319	30626396	6p21.3	6p21.33		611982	"MRPS18B, MRPS18-2"	Mitochondrial ribosomal protein S18B	MRPS18B	28973	ENSG00000204568	pseudogenes on chromosomes 1 and 2		Mrps18b (MGI:1914223)			
chr6	30626456	30646822	6p21.33	6p21.33		615556	"ATAT1, MEC17, C6orf134"	Alpha-tubulin acetyltransferase 1	ATAT1	79969	ENSG00000137343			Atat1 (MGI:1913869)			
chr6	30653118	30673052	6p21.3	6p21.33		603405	"DHX16, DDX16, DBP2, PRP8"	DEAH (Asp-Glu-Ala-His) box polypeptide 16	DHX16	8449	ENSG00000204560			Dhx16 (MGI:1916442)			
chr6	30676388	30687894	6p21.3	6p21.33		610990	"PPP1R18, KIAA1949"	Protein phosphatase 1 regulatory subunit 18	PPP1R18	170954	ENSG00000146112			Ppp1r18 (MGI:1923698)			
chr6	30699806	30717987	6pter-p21.3	6p21.33		607593	"MDC1, NFBD1, KIAA0170"	Mediator of DNA damage checkpoint protein 1	MDC1	9656	ENSG00000137337			Mdc1 (MGI:3525201)			
chr6	30720200	30725425	6p21.3	6p21.33		191130	"TUBB, TUBB5, M40, CDCBM6, CSCSC1"	"Tubulin, beta polypeptide"	TUBB	203068	ENSG00000196230		"Cortical dysplasia, complex, with other brain malformations 6, 615771 (3), Autosomal dominant; Symmetric circumferential skin creases, congenital, 1, 156610 (3), Autosomal dominant"	Tubb5 (MGI:107812)			
chr6	30727708	30742850	6p21.3	6p21.33		606998	FLOT1	Flotillin 1	FLOT1	10211	ENSG00000137312			Flot1 (MGI:1100500)			
chr6	30743198	30744549	6p21.3	6p21.33		602996	"IER3, DIF2, IEX1, PRG1, GLY96"	Immediate early response-3	IER3	8870	ENSG00000137331			Ier3 (MGI:104814)			
chr6	30880957	30900155	6p21.3	6p21.33		600408	"NEP, EDDR1, NTRK4, TRKE"	Neuroepithelial tyrosine kinase	DDR1	780	ENSG00000204580			Ddr1 (MGI:99216)			
chr6	30908199	30914102	6p21.3	6p21.33		601760	GTF2H4	"General transcription factor IIH, polypeptide 4"	GTF2H4	2968	ENSG00000213780			Gtf2h4 (MGI:1338799)			
chr6	30914207	30926458	6p21.3	6p21.33		612802	"VARS2, KIAA1885, COXPD20"	Valyl-tRNA synthetase 2	VARS2	57176	ENSG00000137411		"Combined oxidative phosphorylation deficiency 20, 615917 (3), Autosomal recessive"	Vars2 (MGI:1916165)			
chr6	30940999	30954220	6p21.3	6p21.33		613928	"DPCR1, C6orf37"	Diffuse panbronchiolitis critical region gene 1	MUCL3	135656	ENSG00000168631			Dpcr1 (MGI:2685476)			
chr6	30983707	30989902	6p21.33	6p21.33		616991	"MUC21, C6orf205"	"Mucin 21, cell surface-associated"	MUC21	394263	ENSG00000204544						
chr6	31005951	31035401	6p21.3	6p21.33		613917	"MUC22, PBMUCL1"	Mucin 22	MUC22	100507679	ENSG00000261272						
chr6	31053449	31059889	6p21.3	6p21.33		613918	"HCG22, PBMUCL2"	HLA complex group 22	HCG22	285834							
chr6	31114830	31140091	6p21.3	6p21.33		613525	"SEEK1, C6orf16, PSORS1C1"	SEEK1 gene	PSORS1C1	170679	ENSG00000204540						
chr6	31115087	31120474	6p21.3	6p21.33		602593	"CDSN, HTSS1, HYPT2, PSS1"	Corneodesmosin	CDSN	1041	ENSG00000204539		"Hypotrichosis 2, 146520 (3), Autosomal dominant; Peeling skin syndrome 1, 270300 (3), Autosomal recessive"				
chr6	31142438	31158237	6p21.3	6p21.33		605310	"CCHCR1, HCR, C6orf18"	Coiled-coil alpha-helical rod protein 1	CCHCR1	54535	ENSG00000204536	?role in psoriasis		Cchcr1 (MGI:2385321)			
chr6	31158523	31164214	6p21.3	6p21.33		600912	"TCF19, SC1"	Transcription factor-19 (SC1)	TCF19	6941	ENSG00000137310			Tcf19 (MGI:103180)			
chr6	31164336	31170692	6p21.3	6p21.33		164177	"POU5F1, OTF3, OCT3"	"Pou domain, class 5, transcription factor 1 (octamer-binding transcription factor 3)"	POU5F1	5460	ENSG00000204531	OTF3L on 12; ?related pseudogene on chr.8		Pou5f1 (MGI:101893)			
chr6	31268748	31272135	6p21.3	6p21.33		142840	"HLA-C, PSORS1"	"Major histocompatibility complex, class I, C"	HLA-C	3107	ENSG00000204525		"{HIV-1 viremia, susceptibility to}, 609423 (3); {Psoriasis susceptibility 1}, 177900 (3), Multifactorial"				
chr6	31353865	31357244	6p21.3	6p21.33		142830	"HLA-B, SPDA1"	"Major histocompatibility complex, class I, B"	HLA-B	3106	ENSG00000234745		"{Abacavir hypersensitivity, susceptibility to} (3); {Drug-induced liver injury due to flucloxacillin} (3); {Spondyloarthropathy, susceptibility to, 1}, 106300 (3), Multifactorial; {Stevens-Johnson syndrome, susceptibility to}, 608579 (3); {Synovitis, chronic, susceptibility to} (3); {Toxic epidermal necrolysis, susceptibility to}, 608579 (3)"				
chr6	31399783	31415314	6p21.3	6p21.33		600169	MICA	MHC class I polypeptide-related sequence A	MICA	100507436	ENSG00000204520						
chr6	31463179	31465808	6p21.3	6p21.33		604676	"HCP5, 6S2650E"	"Major histocompatibility complex, class I, gene P5-1"	HCP5	10866							
chr6	31494880	31511123	6p21.3	6p21.33		602436	MICB	MHC class I polypeptide-related sequence B	MICB	4277	ENSG00000204516			Mill2 (MGI:2179989)			
chr6	31528961	31530230	6p21.3	6p21.33		609624	MCCD1	Mitochondrial coiled-coil domain 1	MCCD1	401250	ENSG00000204511						
chr6	31530218	31542474	6p21.3	6p21.33		142560	"DDX39B, BAT1, D6S81E"	DEAD box polypeptide 39Bipt-1	DDX39B	7919	ENSG00000198563	"5 BATs in 160kb segment including also TNFA, TNFB"		Ddx39b (MGI:99240)			
chr6	31544450	31546847	6p21.3	6p21.33		606853	"ATP6V1G2, ATP6G"	"ATPase, H+ transporting, lysosomal, 13kD, V1 subunit G isoform 2"	ATP6V1G2	534	ENSG00000213760			Atp6v1g2 (MGI:1913487)			
chr6	31546850	31558828	6p21.3	6p21.33		601022	NFKBIL1	Nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1	NFKBIL1	4795	ENSG00000204498		"{Rheumatoid arthritis, susceptibility to}, 180300 (3)"	Nfkbil1 (MGI:1340031)			
chr6	31560549	31574323	6p21.3	6p21.33		153440	"LTA, TNFB"	Lymphotoxin alpha (formerly tumor necrosis factor beta)	LTA	4049	ENSG00000226979	cen-DR-21OH-C4-BF-C2-TNF-LTA-HLA-B	"{Leprosy, susceptibility to, 4}, 610988 (3); {Myocardial infarction, susceptibility to}, 608446 (3); {Psoriatic arthritis, susceptibility to}, 607507 (3)"	Lta (MGI:104797)			
chr6	31575566	31578335	6p21.3	6p21.33		191160	"TNF, TNFA"	Tumor necrosis factor (cachectin)	TNF	7124	ENSG00000232810	5'-LTA--TNF-3' in 7kb segment (pter-cen); 210kb from HLA-B	"{Asthma, susceptibility to}, 600807 (3), Autosomal dominant; {Dementia, vascular, susceptibility to} (3); {Malaria, cerebral, susceptibility to}, 611162 (3); {Migraine without aura, susceptibility to}, 157300 (3), Autosomal dominant; {Septic shock, susceptibility to} (3)"	Tnf (MGI:104798)			
chr6	31580557	31582424	6p21.3	6p21.33		600978	"LTB, TNFC"	Lymphotoxin B	LTB	4050	ENSG00000227507			Ltb (MGI:104796)			
chr6	31586178	31588908	6p21.3-p21.1	6p21.33		109170	"LST1, D6S49E, B144"	Leukocyte-specific transcript 1 (B144 protein)	LST1	7940	ENSG00000204482	10kb 3' from TNFA					
chr6	31588882	31593023	6p21.3	6p21.33		611550	"NCR3, 1C7, NKP30, CD337, MALS"	Natural cytotoxicity triggering receptor 3	NCR3	259197	ENSG00000204475		"{Malaria, mild, susceptibility to}, 609148 (3)"				
chr6	31615208	31617024	6p21.3	6p21.33		601833	"AIF1, IRT1"	Allograft inflammatory factor 1	AIF1	199	ENSG00000204472	part of TNF block		Aif1 (MGI:1343098)			
chr6	31620672	31637779	6p21.3	6p21.33		142580	"PRRC2A, BAT2, D6S51E"	Proline-rich coiled-coil protein 2A	PRRC2A	7916	ENSG00000204469			Prrc2a (MGI:1915467)			
chr6	31639027	31660899	6p21.3	6p21.33		142590	"BAG6, BAT3, D6S52E"	BCL2-associated athanogene 6	BAG6	7917	ENSG00000204463			Bag6 (MGI:1919439)			
chr6	31661228	31666282	6p21.3	6p21.33		142610	"GPANK1, BAT4, D6S54E"	G patch domain- and ankyrin repeats-containing protein 1	GPANK1	7918	ENSG00000204438			Gpank1 (MGI:2148975)			
chr6	31665879	31670069	6p21.3	6p21.33		115441	CSNK2B	"Casein kinase-2, beta polypeptide"	CSNK2B	1460	ENSG00000204435			Csnk2b (MGI:88548)			
chr6	31670950	31672449	6p21.3	6p21.33		610433	"LY6G5B, G5B"	"Lymphocyte antigen 6 complex, locus G5B"	LY6G5B	58496	ENSG00000240053			Ly6g5b (MGI:2385809)			
chr6	31676683	31680372	6p21.3	6p21.33		610434	"LY6G5C, G5C"	"Lymphocyte antigen 6 complex, locus G5C"	LY6G5C	80741	ENSG00000204428			Ly6g5c (MGI:2148974)			
chr6	31686948	31703359	6p21.3	6p21.33		142620	"ABHD16A, BAT5, D6S82E"	Abhydrolase domain-containing 16A	ABHD16A	7920	ENSG00000204427			Abhd16a (MGI:99476)			
chr6	31711975	31714064	6p21.3	6p21.33		610437	"LY6G6E, G6E"	"Lymphocyte antigen 6 complex, locus G6E"	LY6G6E	79136							
chr6	31715355	31717803	6p21.3	6p21.33		606038	"LY6G6D, MEGT1, G6D, C6orf23"	"Lymphocyte antigen 6 complex, locus G6D"	LY6G6D	58530	ENSG00000244355			Ly6g6d (MGI:2148931)			
chr6	31718647	31721733	6p21.3	6p21.33		610435	"LY6G6C, G6C"	"Lymphocyte antigen 6 complex, locus G6C"	LY6G6C	80740	ENSG00000204421			Ly6g6c (MGI:2148930)			
chr6	31720556	31726709	6p21.33	6p21.33		606520	"G6B, C6orf25, THAMY"	G6B protein	MPIG6B	80739	ENSG00000204420	mutation identified in 1 THAMY family	"?Thrombocytopenia, anemia, and myelofibrosis, 617441 (3), Autosomal recessive"	Mpig6b (MGI:2146995)			
chr6	31727036	31730264	6p21.3	6p21.33		604744	DDAH2	Dimethylarginine dimethylaminohydrolase-2	DDAH2	23564	ENSG00000213722			Ddah2 (MGI:1859016)			
chr6	31739947	31762677	6p21.33	6p21.33		603382	"MSH5, POF13"	"MutS, E. coli, homolog of, 5"	MSH5	4439	ENSG00000204410	mutation identified in POF13 family	"?Premature ovarian failure 13, 617442 (3), Autosomal recessive"	Msh5 (MGI:1329021)			
chr6	31764134	31777330	6p21.33	6p21.33		609693	"VWA7, C6orf27, G7C"	von Willebrand factor A domain-containing protein 7	VWA7	80737	ENSG00000204396			Vwa7 (MGI:1306798)			
chr6	31777517	31795934	6p21.3	6p21.33		192150	"VARS, VARS1, G7A, VARS2, NDMSCA"	Valyl-tRNA synthetase	VARS	7407	ENSG00000204394		"Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, 617802 (3), Autosomal recessive"	Vars (MGI:90675)			
chr6	31797391	31806983	6p21.3	6p21.33		607282	"LSM2, C6orf28"	LSM2 protein	LSM2	57819	ENSG00000204392			Lsm2 (MGI:90676)			
chr6	31809618	31815057	6p21.3	6p21.33		140559	HSPA1L	Heat-shock 70kD protein-like-1	HSPA1L	3305	ENSG00000204390			Hspa1l (MGI:96231)			
chr6	31815513	31817941	6p21.3	6p21.33		140550	HSPA1A	Heat-shock 70kD protein-1A	HSPA1A	3303	ENSG00000204389	"also 14q22-q24, chr.21, and at least 1 other chromosome"		Hspa1a (MGI:96244)			
chr6	31827734	31830253	6p21.3	6p21.33		603012	HSPA1B	Heat-shock 70kD protein-1B	HSPA1B	3304	ENSG00000204388			Hspa1a (MGI:96244)			
chr6	31834914	31839765	6p21.3	6p21.33		605447	G8	G8 protein	C6orf48	50854	ENSG00000204387						
chr6	31859051	31862931	6p21.3	6p21.33		608272	"NEU1, NEU, SIAL1"	Neuraminidase 1 (lysosomal sialidase; sialidase 1)	NEU1	4758	ENSG00000204386		"Sialidosis, type I, 256550 (3), Autosomal recessive; Sialidosis, type II, 256550 (3), Autosomal recessive"	Neu1 (MGI:97305)			
chr6	31863191	31879045	6p21.3	6p21.33		606107	"SLC44A4, CTL4, C6orf29, DFNA72"	"Solute carrier family 44, member 4"	SLC44A4	80736	ENSG00000204385	mutation identified in 1 DFNA72 family	"?Deafness, autosomal dominant 72, 617606 (3), Autosomal dominant"	Slc44a4 (MGI:1917379)			
chr6	31879758	31897706	6p21.3	6p21.33		604599	"EHMT2, GAT8, G9A, NG36"	Euchromatic histone-lysine N-methyltransferase 2	EHMT2	10919	ENSG00000204371			Ehmt2 (MGI:2148922)			
chr6	31897784	31945673	6p21.3	6p21.33		613927	"C2, ARMD14"	Complement component-2	C2	717	ENSG00000166278	no crossover with BF	"C2 deficiency, 217000 (3), Autosomal recessive; {Macular degeneration, age-related, 14, reduced risk of}, 615489 (3)"	C2 (MGI:88226)			
chr6	31945943	31952083	6p21.3	6p21.33		138470	"CFB, BF, GBG, AHUS4, ARMD14, CFBD"	Complement factor B	CFB	629	ENSG00000243649	mutation identified in 1 CFBD family	"?Complement factor B deficiency, 615561 (3); {Hemolytic uremic syndrome, atypical, susceptibility to, 4}, 612924 (3), Autosomal dominant; {Macular degeneration, age-related, 14, reduced risk of}, 615489 (3)"	Cfb (MGI:105975)			
chr6	31952086	31959086	6p21.3	6p21.33		154040	RDBP	RD RNA-binding protein	NELFE	7936	ENSG00000204356	between C4 and BF		Nelfe (MGI:102744)			
chr6	31958803	31969851	6p21	6p21.33		600478	"SKIV2L, SKI2, SKI2W, THES2"	"Superkiller viralicidic activity 2, S. cerevisiae, homolog, like"	SKIV2L	6499	ENSG00000204351		"Trichohepatoenteric syndrome 2, 614602 (3), Autosomal recessive"	Skiv2l (MGI:1099835)			
chr6	31969810	31972289	6p21.3	6p21.33		605996	DOM3Z	"DOM3, C. elegans, homolog of, Z"	DXO	1797	ENSG00000204348			Dxo (MGI:1890444)			
chr6	31971174	31981445	6p21.3	6p21.33		604977	STK19	Serine/threonine protein kinase 19	STK19	8859	ENSG00000204344			Stk19 (MGI:1860085)			
chr6	31982056	32002679	6p21.3	6p21.33		120810	"C4A, C4S, C4AD"	Complement component-4A	C4A	720	ENSG00000244731	"order:  HLA-B, C2, BF, C4A, C4B, CYP21, DR"	"[Blood group, Rodgers], 614374 (3); C4a deficiency, 614380 (3), Autosomal recessive"	"C4b,C4a (MGI:98320,MGI:88228)"			
chr6	32014794	32035417	6p21.3	6p21.33		120820	"C4B, C4F, C4BD"	Complement component-4B	C4B	721	ENSG00000224389	10kb from C4S	"C4B deficiency, 614379 (3)"	"C4b,C4a (MGI:98320,MGI:88228)"			
chr6	32038315	32041669	6p21.3	6p21.33		613815	"CYP21A2, CYP21, CA21H"	"Cytochrome P450, subfamily XXIA, polypeptide 2 (steroid 21-hydroxylase)"	CYP21A2	1589	ENSG00000231852	"linked to C2, C4, BF; 2 loci, A and B; only B active; pseudogene CYP21P contiguous on 6p"	"Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910 (3), Autosomal recessive; Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910 (3), Autosomal recessive"	Cyp21a1 (MGI:88591)			
chr6	32041154	32109373	6p21.3	6p21.33-p21.32		600985	"TNXB, TNX, TNXB1, TNXBS, TNXB2, EDSCLL, VUR8"	Tenascin XB	TNXB	7148	ENSG00000168477		"Ehlers-Danlos syndrome, classic-like, 606408 (3), Autosomal recessive; Vesicoureteral reflux 8, 615963 (3), Autosomal dominant"	Tnxb (MGI:1932137)			
chr6	32115267	32128239	6p21.3	6p21.32		600984	"ATF6B, CREBL1"	Activating transcription factor 6 beta	ATF6B	1388	ENSG00000213676			Atf6b (MGI:105121)			
chr6	32128706	32130289	6p21.3	6p21.32		617076	"FKBPL, DIR1, WISP39"	FK506-binding protein-like	FKBPL	63943	ENSG00000204315			Fkbpl (MGI:1932127)			
chr6	32153451	32163680	6p21.3	6p21.32		603298	PPT2	Palmitoyl-protein thioesterase-2	PPT2	9374	ENSG00000221988			Ppt2 (MGI:1860075)			
chr6	32164604	32168284	6p21.32	6p21.32		609897	EGFL8	Epidermal growth factor-like 8	EGFL8	80864	ENSG00000241404			Egfl8 (MGI:1932094)			
chr6	32168205	32178110	6p21.3	6p21.32		603099	"AGPAT1, LPAATA"	1-acylglycerol-3-phosphate O-acyltransferase 1 (lysophosphatidic acid acyltransferase-alpha)	AGPAT1	10554	ENSG00000204310			Agpat1 (MGI:1932075)			
chr6	32178384	32180792	6p21.3	6p21.32		602677	"RNF5, RING5"	RING finger protein-5	RNF5	6048	ENSG00000204308			Rnf5 (MGI:1860076)			
chr6	32180967	32184379	6p21.3	6p21.32		600214	"AGER, RAGE"	Advanced glycosylation end product-specific receptor	AGER	177	ENSG00000204305	"at junction of classes II, III MHC"		Ager (MGI:893592)			
chr6	32184732	32190185	6p21.3	6p21.32		176311	"PBX2, HOX12, G17"	Pre-B-cell leukemia transcription factor-2	PBX2	5089	ENSG00000204304			Pbx2 (MGI:1341793)			
chr6	32194842	32224066	6p21.3	6p21.32		164951	"NOTCH4, INT3"	"Notch, Drosophila, homolog of, 4"	NOTCH4	4855	ENSG00000204301			Notch4 (MGI:107471)			
chr6	32393338	32408878	6p21.3	6p21.32		606000	"BTNL2, SS2"	Butyrophilin-like protein 2	BTNL2	56244	ENSG00000204290		"{Sarcoidosis, susceptibility to, 2}, 612387 (3), Autosomal dominant"	Btnl2 (MGI:1859549)			
chr6	32439841	32445045	6p21.3	6p21.32		142860	HLA-DRA	"Major histocompatibility complex, class II, DR alpha"	HLA-DRA	3122	ENSG00000204287	"1 alpha, 3 different beta chains"		H2-Ea-ps (MGI:95900)			
chr6	32517342	32530315	6p21.3	6p21.32		604776	HLA-DRB5	"Major histocompatibility complex, class II, DR beta-5"	HLA-DRB5	3127	ENSG00000198502			H2-Eb1 (MGI:95901)			
chr6	32578768	32589835	6p21.3	6p21.32		142857	"HLA-DRB1, SS1"	"Major histocompatibility complex, class II, DR beta-1"	HLA-DRB1	3123	ENSG00000196126		"{Multiple sclerosis, susceptibility to, 1}, 126200 (3), Multifactorial; {Sarcoidosis, susceptibility to, 1}, 181000 (3), Autosomal dominant"				
chr6	32637405	32654845	6p21.3	6p21.32		146880	"HLA-DQA1, CELIAC1"	"Major histocompatibility complex, class II, DQ alpha-1"	HLA-DQA1	3117	ENSG00000196735		"{Celiac disease, susceptibility to}, 212750 (3), Autosomal recessive, Multifactorial"	H2-Aa (MGI:95895)			
chr6	32659463	32666688	6p21.3	6p21.32		604305	"HLA-DQB1, CELIAC1"	"Major histocompatibility complex, class II, DQ beta-1"	HLA-DQB1	3119	ENSG00000179344		"{Celiac disease, susceptibility to}, 212750 (3), Autosomal recessive, Multifactorial; {Creutzfeldt-Jakob disease, variant, resistance to}, 123400 (3), Autosomal dominant; {Multiple sclerosis, susceptibility to, 1}, 126200 (3), Multifactorial"	H2-Ab1 (MGI:103070)			
chr6	32741385	32746886	6p21.32	6p21.32		613503	"HLA-DQA2, HLA-DXA"	"Major histocompatibility complex, class II, DQ alpha-2"	HLA-DQA2	3118	ENSG00000237541						
chr6	32756093	32763552	6p21.32	6p21.32		615161	"HLA-DQB2, HLA-DXB"	"Major histocompatibility complex, class II, DQ beta-2"	HLA-DQB2	3120	ENSG00000232629						
chr6	32812762	32817047	6p21.3	6p21.32		600629	HLA-DOB	"Major histocompatibility complex, class II, DO beta"	HLA-DOB	3112	ENSG00000241106			H2-Ob (MGI:95925)			
chr6	32821832	32838822	6p21.3	6p21.32		170261	"TAP2, ABCB3, PSF2, RING11"	"Transporter 2, ATP-binding cassette, subfamily B"	TAP2	6891	ENSG00000204267	tel-TAP1-LMP2-LMP1-TAP2-cen	"Bare lymphocyte syndrome, type I, due to TAP2 deficiency, 604571 (3), Autosomal recessive; Wegener-like granulomatosis (3)"	Tap2 (MGI:98484)			
chr6	32840716	32844934	6p21.3	6p21.32		177046	"PSMB8, LMP7, RING10, JMP, NKJO, ALDD"	"Proteasome subunit, beta type, 8 (large multifunctional protease-7)"	PSMB8	5696	ENSG00000204264	between TAP1 and TAP2	"Autoinflammation, lipodystrophy, and dermatosis syndrome, 256040 (3), Autosomal recessive"	Psmb8 (MGI:1346527)			
chr6	32845208	32853970	6p21.3	6p21.32		170260	"TAP1, ABCB2, RING4, PSF1"	"Transporter 1, ATP-binding cassette, subfamily B"	TAP1	6890	ENSG00000168394	~7kb telomeric to TAP2	"Bare lymphocyte syndrome, type I, 604571 (3), Autosomal recessive"	Tap1 (MGI:98483)			
chr6	32854160	32859850	6p21.3	6p21.32		177045	"PSMB9, LMP2, RING12"	"Proteasome subunit, beta type, 9"	PSMB9	5698	ENSG00000240065	just centromeric to TAP1		Psmb9 (MGI:1346526)			
chr6	32934628	32941069	6p21.3	6p21.32		142856	"HLA-DMB, RING7"	"Major histocompatibility complex, class II, DM beta"	HLA-DMB	3109	ENSG00000242574			"H2-DMb2,H2-DMb1 (MGI:95922,MGI:95923)"			
chr6	32948613	32953121	6p21.3	6p21.32		142855	"HLA-DMA, RING6"	"Major histocompatibility complex, class II, DM alpha"	HLA-DMA	3108	ENSG00000204257			H2-DMa (MGI:95921)			
chr6	32968659	32981504	6p21.3	6p21.32		601540	"BRD2, RING3, FSRG1"	Bromodomain-containing protein 2	BRD2	6046	ENSG00000204256	between HLA-DNA and HLA-DMA		Brd2 (MGI:99495)			
chr6	33004181	33009611	6p21.3	6p21.32		142930	HLA-DNA	"Major histocompatibility complex, class II, DN alpha"	HLA-DOA	3111	ENSG00000204252			H2-Oa (MGI:95924)			
chr6	33064568	33080777	6p21.3	6p21.32		142880	"HLA-DPA1, HLADP"	"Major histocompatibility complex, class II, DP alpha-1"	HLA-DPA1	3113	ENSG00000231389	"2 different alpha, 2 different beta chains"					
chr6	33075925	33089695	6p21.3	6p21.32		142858	HLA-DPB1	"Major histocompatibility complex, class II, DP beta-1"	HLA-DPB1	3115	ENSG00000223865		"{Beryllium disease, chronic, susceptibility to} (3)"				
chr6	33162691	33193008	6p21.3	6p21.32		120290	"COL11A2, DFNA13, DFNB53, FBCG2, OSMEDA, OSMEDB"	"Collagen XI, alpha-2 polypeptide"	COL11A2	1302	ENSG00000204248	45kb centromeric of HLA-DPB2; 3'--5'-cen	"Deafness, autosomal dominant 13, 601868 (3), Autosomal dominant; Deafness, autosomal recessive 53, 609706 (3), Autosomal recessive; Fibrochondrogenesis 2, 614524 (3), Autosomal recessive, Autosomal dominant; Otospondylomegaepiphyseal dysplasia, autosomal dominant, 184840 (3), Autosomal dominant; Otospondylomegaepiphyseal dysplasia, autosomal recessive, 215150 (3), Autosomal recessive"	Col11a2 (MGI:88447)			
chr6	33193584	33200990	6p21.3	6p21.32		180246	RXRB	"Retinoid X receptor, beta"	RXRB	6257	ENSG00000204231			Rxrb (MGI:98215)			
chr6	33200825	33204436	6p21.3	6p21.32		601416	"SLC39A7, D6S2244E, HKE4"	"Solute carrier family 39 (zinc transporter), member 7 (Ke4 gene, mouse, homolog of)"	SLC39A7	7922	ENSG00000112473			Slc39a7 (MGI:95909)			
chr6	33204636	33206830	6p21.3	6p21.32		601417	"HSD17B8, FABGL, D6S2245E, HKE6"	"Hydroxysteroid (17-beta) dehydrogenase 8 (Ke6 gene, mouse, homolog of)"	HSD17B8	7923	ENSG00000204228			H2-Ke6 (MGI:95911)			
chr6	33207834	33207943	6p21.32	6p21.32		611500	"MRI219-1, MIRN219-1"	Micro RNA 219-1	MIR219A1	407002							
chr6	33208508	33212721	6p21.3	6p21.32		602045	"RING1, RNF1"	RING finger protein-1	RING1	6015	ENSG00000204227			Ring1 (MGI:1101770)			
chr6	33250271	33271964	6p21.3	6p21.32		603443	"VPS52, SACM2L"	Vacuolar protein sorting 52 homolog (S. cerevisiae)	VPS52	6293	ENSG00000223501			Vps52 (MGI:1330304)			
chr6	33272074	33276503	6p21.3	6p21.32		180473	RPS18	Ribosomal protein S18	RPS18	6222	ENSG00000231500			Rps18 (MGI:98146)			
chr6	33277139	33278824	6p21.3	6p21.32		603095	B3GALT4	"UDP-galactose:beta-N-acetylglucosamine beta-1,3-galactosyltransferase 4"	B3GALT4	8705	ENSG00000235863			B3galt4 (MGI:1859517)			
chr6	33278206	33289526	6p21.3	6p21.32		611440	"WDR46, BING4"	WD repeat-containing protein 46	WDR46	9277	ENSG00000227057			Wdr46 (MGI:1931871)			
chr6	33291653	33299387	6p21.3	6p21.32		602306	RAB2L	"RAB2, member RAS oncogene family-like"	RGL2	5863	ENSG00000237441			Rgl2 (MGI:107483)			
chr6	33299693	33314386	6p21.3	6p21.32		601962	"TAPBP, TPSN"	TAP-binding protein (tapasin)	TAPBP	6892	ENSG00000231925		"Bare lymphocyte syndrome, type I, 604571 (3), Autosomal recessive"	Tapbp (MGI:1201689)			
chr6	33314404	33317941	6p21.3	6p21.32		611439	"ZBTB22, BING1"	Zinc finger- and BTB domain-containing protein 22	ZBTB22	9278	ENSG00000236104			Zbtb22 (MGI:1931870)			
chr6	33318557	33323015	6p21.3	6p21.32		603186	DAXX	Death-associated protein 6	DAXX	1616	ENSG00000204209			Daxx (MGI:1197015)			
chr6	33391523	33410225	6p21.3	6p21.32		603763	"KIFC1, KNSL2, HSET"	Kinesin family member C1	KIFC1	3833	ENSG00000237649			"Kifc1,Kifc5b (MGI:2137414,MGI:109596)"			
chr6	33410750	33416452	6p21.3	6p21.32		602881	PHF1	PHD finger protein-1	PHF1	5252	ENSG00000112511			Phf1 (MGI:98647)			
chr6	33416541	33418287	6p21.32	6p21.32		616953	"CUTA, ACHAP, C6orf82"	"CutA, E. coli, homolog of"	CUTA	51596	ENSG00000112514			Cuta (MGI:1914925)			
chr6	33420069	33453688	6p21.3	6p21.32		603384	"SYNGAP1, MRD5"	Synaptic Ras GTPase activating protein 1	SYNGAP1	8831	ENSG00000197283		"Mental retardation, autosomal dominant 5, 612621 (3), Autosomal dominant"	Syngap1 (MGI:3039785)			
chr6	33500000	36600000	6p21.31			612893	STQTL19	Stature quantitative trait locus 19		100302684		associated with rs1776897	"{Stature QTL 19}, 612893 (2)"				
chr6	33572545	33580295	6p21.3-p21.2	6p21.31		600516	BAK1	BCL2-antagonist/killer 1	BAK1	578	ENSG00000030110	centromeric to MHC region		Bak1 (MGI:1097161)			
chr6	33621332	33696573	6pter-p21	6p21.31		147267	ITPR3	"Inositol 1,4,5-triphosphate receptor, type 3"	ITPR3	3710	ENSG00000096433		"{Diabetes, type 1, susceptibility to}, 222100 (2), Autosomal recessive"	Itpr3 (MGI:96624)			
chr6	33696760	33711750	6p21.31	6p21.31		614461	"UQCC2, C6orf126, M19"	Ubiquinol-cytochrome c reductase complex assembly factor 2	UQCC2	84300	ENSG00000137288	mutation identified in 1 MC3DN7 patient	"?Mitochondrial complex III deficiency, nuclear type 7, 615824 (3), Autosomal recessive"	Uqcc2 (MGI:1914517)			
chr6	33721475	33755670	6p21	6p21.31		606993	"IHPK3, INSP6K3, IP6K3"	Inositol hexaphosphate kinase 3	IP6K3	117283	ENSG00000161896	pseudogene on 6p24.1		Ip6k3 (MGI:3045325)			
chr6	33771212	33794273	6p21.31	6p21.31		616312	"LEMD2, NET25, CTRCT42"	LEM domain-containing protein 2	LEMD2	221496	ENSG00000161904		"Cataract 46, juvenile-onset, 212500 (3), Autosomal recessive"	Lemd2 (MGI:2385045)			
chr6	33794671	33804015	6p21.3	6p21.31		158270	MLN	Motilin	MLN	4295	ENSG00000096395						
chr6	34018642	34155621	6p21.3	6p21.31		604100	"GRM4, MGLUR4"	"Glutamate receptor, metabotropic, 4"	GRM4	2914	ENSG00000124493			Grm4 (MGI:1351341)			
chr6	34236799	34246230	6p21	6p21.31		600701	"HMGA1, HMGIY"	High-mobility group AT-hook 1	HMGA1	3159	ENSG00000137309		"{Diabetes mellitus, noninsulin-dependent, susceptibility to}, 125853 (3), Autosomal dominant"	"Hmga1,Hmga1b (MGI:96161,MGI:96160)"			
chr6	34246379	34249107	6p21.3	6p21.31		611419	"C6orf1, LBH"	"Chromosome 6, open reading frame 1"	SMIM29	221491	ENSG00000186577	"opposite strand, tail-to-tail with HMGA1"					
chr6	34417453	34426124	6p	6p21.31		603632	"RPS10, DBA9"	Ribosomal protein S10	RPS10	6204	ENSG00000124614		"Diamond-Blackfan anemia 9, 613308 (3), Autosomal dominant"	Rps10 (MGI:1914347)			
chr6	34466060	34536261	6p21	6p21.31		606512	"PACSIN1, KIAA1379"	Protein kinase C and casein kinase substrate in neurons 1	PACSIN1	29993	ENSG00000124507			Pacsin1 (MGI:1345181)			
chr6	34537799	34556332	6p21.3	6p21.31		608144	"SPDEF, PDEF"	SAM pointed domain-containing ETS transcription factor	SPDEF	25803	ENSG00000124664			Spdef (MGI:1353422)			
chr6	34587279	34696849	6p21.31	6p21.31		612217	C6orf106	Chromosome 6 open reading frame 106	C6orf106	64771	ENSG00000196821			D17Wsu92e (MGI:106281)			
chr6	34757093	34773856	6p21.31	6p21.31		603522	SNRPC	Small nuclear ribonucleoprotein polypeptide C	SNRPC	6631	ENSG00000124562						
chr6	34877777	34888070	6p21.31	6p21.31		600772	"TAF11, TAF2I, TAFII28"	"TAF11 RNA polymerase II, TATA box-binding protein-associated factor, 28kD"	TAF11	6882	ENSG00000064995			Taf11 (MGI:1916026)			
chr6	34889260	35097991	6p21.3	6p21.31		608994	"ANKS1, ODIN, KIAA0229"	Ankyrin repeat and sterile alpha motif domains-containing protein 1	ANKS1A	23294	ENSG00000064999			Anks1 (MGI:2446180)			
chr6	35118070	35141409	6p21.3-p21.2	6p21.31		186982	"TCP11, D6S230E"	T-complex homolog tcp-11	TCP11	6954	ENSG00000124678	expressed only in testis at same time as ZNF76 (day 20 after birth)		Tcp11 (MGI:98544)			
chr6	35214046	35253078	6p21.3	6p21.31		614708	SCUBE3	"Signal peptide-, CUB domain-,  and EGF-like domains-containing protein 3"	SCUBE3	222663	ENSG00000146197			Scube3 (MGI:3045253)			
chr6	35259472	35295986	6p21.3-p21.2	6p21.31		194549	"ZNF76, D6S229E"	Zinc finger protein-76 (expressed in testis)	ZNF76	7629	ENSG00000065029	same 300kb fragment as TCP11		Zfp523 (MGI:2687278)			
chr6	35297817	35321770	6p21.31	6p21.31		610094	"DEF6, IBP, SLAT"	"Def6, mouse, homolog of"	DEF6	50619	ENSG00000023892			Def6 (MGI:1346328)			
chr6	35342557	35428190	6p21.2-p21.1	6p21.31		600409	"PPARD, NUC1"	"Peroxisome proliferative activated receptor, delta"	PPARD	5467	ENSG00000112033			Ppard (MGI:101884)			
chr6	35452338	35467105	6p22-p21	6p21.31		613976	"FANCE, FACE"	"Fanconi anemia, complementation group E gene"	FANCE	2178	ENSG00000112039		"Fanconi anemia, complementation group E, 600901 (3), Autosomal recessive"	Fance (MGI:1920025)			
chr6	35468400	35470780	6p21.31	6p21.31		615660	"RPL10A, CSA19"	Ribosomal protein L10A	RPL10A	4736	ENSG00000198755			Rpl10a (MGI:1343877)			
chr6	35473596	35497083	6p21.3	6p21.31		603170	"TEAD3, TEF5, TEAD5"	TEA domain family member 3 (transcriptional enhancer factor 5)	TEAD3	7005	ENSG00000007866			Tead3 (MGI:109241)			
chr6	35497873	35512937	6p21.3	6p21.31		602280	"TULP1, RP14, LCA15"	Tubby-like protein-1	TULP1	7287	ENSG00000112041		"Leber congenital amaurosis 15, 613843 (3), Autosomal recessive; Retinitis pigmentosa 14, 600132 (3), Autosomal recessive"	Tulp1 (MGI:109571)			
chr6	35573584	35728582	6p21.3-p21.2	6p21.31		602623	"FKBP5, FKBP51"	FK506-binding protein 5	FKBP5	2289	ENSG00000096060		"{Major depressive disorder and accelerated response to antidepressant drug treatment}, 608516 (3)"	Fkbp5 (MGI:104670)			
chr6	35794981	35797343	6pter-p21.1	6p21.31		120105	CLPS	"Colipase, pancreatic"	CLPS	1208	ENSG00000137392			Clps (MGI:88421)			
chr6	35805293	35824074	6p21.3	6p21.31		609427	"LHFPL5, TMHS, DFNB67"	LHFP-like protein 5	LHFPL5	222662	ENSG00000197753		"Deafness, autosomal recessive 67, 610265 (3), Autosomal recessive"	Lhfpl5 (MGI:1915382)			
chr6	35833033	35921179	6p21.31	6p21.31		601939	SRPK1	"Protein kinase, serine/arginine-specific, 1"	SRPK1	6732	ENSG00000096063			Srpk1 (MGI:106908)			
chr6	35943513	36024635	6p21.31	6p21.31		608480	"SLC26A8, TAT1, SPGF3"	"Solute carrier family 26 (sulfate transporter), member 8"	SLC26A8	116369	ENSG00000112053		"Spermatogenic failure 3, 606766 (3), Autosomal dominant"	Slc26a8 (MGI:2385046)			
chr6	36027676	36122963	6p21.3-p21.2	6p21.31		600289	"MAPK14, CSBP1"	Mitogen-activated protein kinase 14 (cytokine suppressive anti-inflammatory drug binding protein 1)	MAPK14	1432	ENSG00000112062			Mapk14 (MGI:1346865)			
chr6	36196772	36232789	6p21.31	6p21.31		616856	"BRPF3, KIAA1286"	Bromodomain- and PHD finger-containing protein 3	BRPF3	27154	ENSG00000096070			Brpf3 (MGI:2146836)			
chr6	36242522	36313954	6p21.31	6p21.31		612121	"PNPLA1, ARCI10"	Patatin-like phospholipase domain-containing protein 1	PNPLA1	285848	ENSG00000180316		"Ichthyosis, congenital, autosomal recessive 10, 615024 (3), Autosomal recessive"	Pnpla1 (MGI:3617850)			
chr6	36354220	36387799	6p21	6p21.31		605255	"ETV7, TEL2, TELB"	ETS variant gene 7	ETV7	51513	ENSG00000010030						
chr6	36442766	36491142	6p21.31	6p21.31		615932	KCTD20	Potassium channel tetramerization domain-containing protein 20	KCTD20	222658	ENSG00000112078			Kctd20 (MGI:1914239)			
chr6	36493881	36547515	6p21	6p21.31		606964	"STK38, NDR"	Serine/threonine protein kinase 38	STK38	11329	ENSG00000112079			Stk38 (MGI:2442572)			
chr6	36594312	36604466	6p21	6p21.3-p21.2		603364	"SRSF3, SFRS3, SRP20"	"Splicing factor, arginine/serine-rich, 3"	SRSF3	6428	ENSG00000112081			Srsf3 (MGI:98285)			
chr6	36600000	40500000	6p21.2			615080	AD17	Alzheimer disease 17		101290498		associated with rs75932628T	"Alzheimer disease 17, 615080 (2)"				
chr6	36600000	40500000	6p21.2			616343	TP53COR1	"Tumor protein p53 pathway corepressor 1, noncoding"	TP53COR1	102800311							
chr6	36673620	36675125	6p21.2	6p21.2		617179	PANDAR	Promoter of CDKN1A antisense DNA damage-activated RNA	PANDAR	101154753							
chr6	36676459	36687338	6p21.2	6p21.2		116899	"CDKN1A, WAF1, CIP1, CDKN1"	"Cyclin-dependent kinase inhibitor 1A (p21, Cip1)"	CDKN1A	1026	ENSG00000124762			Cdkn1a (MGI:104556)			
chr6	36740772	36839443	6p21	6p21.2		604209	"CPNE5, CPN5"	Copine V	CPNE5	57699	ENSG00000124772			Cpne5 (MGI:2385908)			
chr6	36834885	36928963	6p21.2	6p21.2		616642	"C6orf89, BRAP, AMFION"	Bombesin receptor-activated protein	C6orf89	221477	ENSG00000198663			BC004004 (MGI:2136782)			
chr6	36854828	36875023	6p21.1	6p21.2		601301	"PPIL1, CYPL1"	Peptidylprolyl isomerase (cyclophilin)-like 1	PPIL1	51645	ENSG00000137168	previously assigned to chr.2		Ppil1 (MGI:1916066)			
chr6	36968134	36987170	6p21.2	6p21.2		610449	"MTCH1, PSAP"	Mitochondrial carrier homolog 1	MTCH1	23787	ENSG00000137409			Mtch1 (MGI:1929261)			
chr6	37005646	37029071	6p21.2	6p21.2		605091	FGD2	"FYVE, RhoGEF, and PH domain-containing protein 2"	FGD2	221472	ENSG00000146192			Fgd2 (MGI:1347084)			
chr6	37170145	37175427	6p21.2	6p21.2		164960	PIM1	Oncogene PIM1	PIM1	5292	ENSG00000137193			Pim1 (MGI:97584)			
chr6	37257703	37332969	6p21.2	6p21.2		616880	"TBC1D22B, C6orf197"	"TBC1 domain family, member 22B"	TBC1D22B	55633	ENSG00000065491			Tbc1d22b (MGI:2681867)			
chr6	37353971	37394737	6p21.3	6p21.2		611685	"RNF8, KIAA0646"	Ring finger protein 8	RNF8	9025	ENSG00000112130			Rnf8 (MGI:1929069)			
chr6	37433130	37482843	6p21.2	6p21.2		616189	"CMTR1, MTR1, ISG95, FTSJD2, KIAA0082"	CAP methyltransferase 1	CMTR1	23070	ENSG00000137200			Cmtr1 (MGI:1921407)			
chr6	37632507	37697989	6p21	6p21.2		609626	"MDGA1, GPIM"	MAM domain-containing glycosylphosphatidylinositol anchor 1	MDGA1	266727	ENSG00000112139			Mdga1 (MGI:1922012)			
chr6	37819530	38154623	6pter-p22.3	6p21.2		607455	"ZFAND3, TEX27"	Zinc finger AN1 domain-containing protein 3	ZFAND3	60685	ENSG00000156639			Zfand3 (MGI:1096572)			
chr6	38168450	38640540	6p21	6p21.2		611237	"BTBD9, KIAA1880"	BTB/POZ domain-containing protein 9	BTBD9	114781	ENSG00000183826			Btbd9 (MGI:1916625)			
chr6	38675924	38703175	6p21.3-p21.2	6p21.2		138750	GLO1	Glyoxalase I	GLO1	2739	ENSG00000124767	~3cM proximal to HLA		Glo1 (MGI:95742)			
chr6	38715328	39030797	6p21	6p21.2		603337	"DNAH8, HDHC9"	"Dynein, axonemal, heavy chain 8"	DNAH8	1769	ENSG00000124721			Dnah8 (MGI:107714)			
chr6	39048780	39091302	6p21	6p21.2		138032	GLP1R	Glucagon-like peptide 1 receptor	GLP1R	2740	ENSG00000112164			Glp1r (MGI:99571)			
chr6	39188970	39229474	6p21	6p21.2		603493	"KCNK5, TASK2"	"Potassium channel, subfamily K, member 5"	KCNK5	8645	ENSG00000164626			Kcnk5 (MGI:1336175)			
chr6	39299000	39314460	6p21.2-p21.1	6p21.2		607370	"KCNK17, TASK4, TALK2"	"Potassium channel, subfamily K, member 17"	KCNK17	89822	ENSG00000124780						
chr6	39314565	39322991	6p21.2-p21.1	6p21.2		607369	"KCNK16, TALK1"	"Potassium channel, subfamily K, member 16"	KCNK16	83795	ENSG00000095981			Kcnk16 (MGI:1921821)			
chr6	39329989	39725422	6p21	6p21.2		613919	KIF6	Kinesin family member 6	KIF6	221458	ENSG00000164627			Kif6 (MGI:1098238)			
chr6	39792365	39904876	6p21.2	6p21.2		606627	"DAAM2, KIAA0381"	Dishevelled-associated activator of morphogenesis 2	DAAM2	23500	ENSG00000146122			Daam2 (MGI:1923691)			
chr6	39904257	39934550	6p21.3	6p21.2		603707	"MOCS1, MOCODA"	Molybdenum cofactor synthesis-1	MOCS1	4337	ENSG00000124615		"Molybdenum cofactor deficiency A, 252150 (3), Autosomal recessive"				
chr6	40378284	40379898	6p21.2-p21.1	6p21.2		615676	"TDRG1, LINC00532"	"Testis development-related gene 1, noncoding"	TDRG1	732253							
chr6	40391588	40587463	6p21.2	6p21.2-p21.1		612808	"LRFN2, SALM1, KIAA1246"	Leucine-rich repeat and fibronectin type III domain-containing protein 2	LRFN2	57497	ENSG00000156564			Lrfn2 (MGI:1917780)			
chr6	40500000	53000000	6p21.1-p12.2			607498	MGR3	"Migraine with or without aura, susceptibility to, 3"		337892		lod 5.78 at D6S452	"{Migraine with or without aura, susceptibility to, 3}, 607498 (2), Autosomal dominant"				
chr6	40500000	46200000	6p21.1			132100	PPR1	Photoparoxysmal response 1		100528023		max lod at D6S2427	"Photoparoxysmal response 1, 132100 (2), Autosomal dominant"				
chr6	41026900	41039198	6p21.1	6p21.1		617464	"UNC5CL, ZUD"	Unc5 family C-terminal-like protein	UNC5CL	222643	ENSG00000124602			Unc5cl (MGI:1923839)			
chr6	41053200	41064890	6p21	6p21.1		604797	APOBEC2	"Apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2"	APOBEC2	10930	ENSG00000124701			Apobec2 (MGI:1343178)			
chr6	41066787	41097786	6p21.2	6p21.1		614393	"OARD1, C6orf130"	O-acyl-ADP-ribose deacylase 1	OARD1	221443	ENSG00000124596			Oard1 (MGI:2146818)			
chr6	41072967	41102406	6p21.3	6p21.1		189903	NFYA	"Transcription factor NF-Y, A subunit"	NFYA	4800	ENSG00000001167			Nfya (MGI:97316)			
chr6	41149096	41158449	6p21.1	6p21.1		609714	"TREML1, TLT1"	Triggering receptor expressed on myeloid cells-like protein 1	TREML1	340205	ENSG00000161911			Treml1 (MGI:1918576)			
chr6	41158505	41163185	6p21.2	6p21.1		605086	TREM2	Triggering receptor expressed on myeloid cells 2	TREM2	54209	ENSG00000095970		"Nasu-Hakola disease, 221770 (3), Autosomal recessive"	Trem2 (MGI:1913150)			
chr6	41189748	41201232	6p21.1	6p21.1		609715	"TREML2, TLT2"	Triggering receptor expressed on myeloid cells-like protein 2	TREML2	79865	ENSG00000112195			Treml2 (MGI:2147038)			
chr6	41208553	41217946	6p21.1	6p21.1		609716	"TREML3, TLT3"	Triggering receptor expressed on myeloid cells-like protein 3	TREML3P	340206							
chr6	41228286	41239385	6p21	6p21.1		614664	"TREML4, TLT4"	Triggering receptor expressed on myeloid cells-like protein 4	TREML4	285852	ENSG00000188056						
chr6	41267384	41286744	6p21.1	6p21.1		605085	TREM1	Triggering receptor expressed on myeloid cells 1	TREM1	54210	ENSG00000124731			Trem1 (MGI:1930005)			
chr6	41335619	41350886	6p21.1	6p21.1		604531	"NCR2, LY95, NKP44"	"Natural cytotoxicity triggering receptor 2 (lymphocyte antigen 95, mouse, homolog of)"	NCR2	9436	ENSG00000096264						
chr6	41546425	41602383	6p21.1	6p21.1		608924	FOXP4	Forkhead box P4	FOXP4	116113	ENSG00000137166			Foxp4 (MGI:1921373)			
chr6	41637019	41654245	6p21	6p21.1		604971	MDFI	MYOD family inhibitor	MDFI	4188	ENSG00000112559			Mdfi (MGI:107687)			
chr6	41683977	41736258	6p21	6p21.1		600744	"TFEB, TCFEB"	Transcription factor EB	TFEB	7942	ENSG00000112561			Tfeb (MGI:103270)			
chr6	41736710	41747400	6p21.3-p21.1	6p21.1		169740	PGC	Preprogastricsin	PGC	5225	ENSG00000096088	cen-PGG-GLO1-HLA		Pgc (MGI:98909)			
chr6	41780761	41787371	6p21.31	6p21.1		611389	"PRICKLE4, C6orf49, OBTP"	"Prickle, Drosophila, homolog of, 4"	PRICKLE4	29964	ENSG00000278224			Prickle4 (MGI:2685785)			
chr6	41787442	41789895	6p21.1	6p21.1		616168	"TOMM6, TOM6"	"Translocase of outer mitochondrial membrane 6, yeast, homolog of"	TOMM6	100188893	ENSG00000214736			Tomm6 (MGI:1913369)			
chr6	41905352	41921146	6p21.1	6p21.1		612915	"MED20, TRFP"	Mediator complex subunit 20	MED20	9477	ENSG00000124641			Med20 (MGI:1929648)			
chr6	41921226	41933045	6p21.1	6p21.1		603871	BYSL	"By the ribosomal protein S6 gene, Drosophila, homolog-like (bystin)"	BYSL	705	ENSG00000112578			Bysl (MGI:1858419)			
chr6	41934932	42048893	6p21	6p21.1		123834	CCND3	Cyclin D3	CCND3	896	ENSG00000112576	pseudogene also on 6p21		Ccnd3 (MGI:88315)			
chr6	42155376	42180082	6p21.1	6p21.1		600364	"GUCA1A, GCAP, COD3, CORD14"	"Guanylate cyclase activator 1A, retina"	GUCA1A	2978	ENSG00000048545		"Cone dystrophy-3, 602093 (3), Autosomal dominant; Cone-rod dystrophy 14, 602093 (3), Autosomal dominant"	Guca1a (MGI:102770)			
chr6	42183283	42194955	6p21.1	6p21.1		602275	"GUCA1B, GCAP2, GUCA2, RP48"	"Guanylate cyclase activator 1B, retina"	GUCA1B	2979	ENSG00000112599		"Retinitis pigmentosa 48, 613827 (3)"	Guca1b (MGI:1194489)			
chr6	42206800	42217894	6p21.1-p12.1	6p21.1		611976	MRPS10	Mitochondrial ribosomal protein S10	MRPS10	55173	ENSG00000048544	"5 pseudogenes on chromosomes 1, 3, and 9"		Mrps10 (MGI:1928139)			
chr6	42224932	42452215	6p21.1	6p21.1		610322	"TRERF1, TREP132"	Transcriptional regulating factor 1	TRERF1	55809	ENSG00000124496			Trerf1 (MGI:2442086)			
chr6	42563904	42693504	6p21.1	6p21.1		609134	"UBR2, C6orf133, KIAA0349"	Ubiquitin-protein ligase E3 component N-recognin 2	UBR2	23304	ENSG00000024048			Ubr2 (MGI:1861099)			
chr6	42694508	42723038	6p21.1-cen	6p21.1		179605	"PRPH2, DS, RP7, PRPH, AVMD, AOFMD, CACD2, MDBS1"	"Peripherin 2, mouse, homolog of"	PRPH2	5961	ENSG00000112619	digenic RP with ROM1	"Choroidal dystrophy, central areolar 2, 613105 (3), Autosomal dominant; Leber congenital amaurosis 18, 608133 (3), Autosomal recessive, Autosomal dominant; Macular dystrophy, patterned, 1, 169150 (3), Autosomal dominant; Macular dystrophy, vitelliform, 3, 608161 (3), Autosomal dominant; Retinitis pigmentosa 7 and digenic, 608133 (3), Autosomal recessive, Autosomal dominant; Retinitis punctata albescens, 136880 (3), Autosomal recessive, Autosomal dominant"	Prph2 (MGI:102791)			
chr6	42744495	42746145	6p21.1	6p21.1		602971	"TBCC, CFC"	Tubulin-specific chaperone C	TBCC	6903	ENSG00000124659			Tbcc (MGI:1919976)			
chr6	42879162	42889895	6p21.1	6p21.1		617417	RPL7L1	Ribosomal protein L7-like 1	RPL7L1	285855	ENSG00000146223			Rpl7l1 (MGI:1913479)			
chr6	42915596	42925837	6p21.3	6p21.1		606817	PTCRA	"Pre-T-cell receptor, alpha-chain precursor"	PTCRA	171558	ENSG00000171611			Ptcra (MGI:104857)			
chr6	42928001	42939286	6pter-p12	6p21.1		610774	"CNPY3, TNRC5, PRAT4A, ERDA5, EIEE60"	"Canopy 3, zebrafish, homolog of"	CNPY3	10695	ENSG00000137161		"Epileptic encephalopathy, early infantile, 60, 617929 (3)"	Cnpy3 (MGI:1919279)			
chr6	42960753	42963879	6p12	6p21.1		606628	GNMT	Glycine N-methyltransferase	GNMT	27232	ENSG00000124713		"Glycine N-methyltransferase deficiency, 606664 (3), Autosomal recessive"	Gnmt (MGI:1202304)			
chr6	42963872	42980223	6p21.1	6p21.1		601498	"PEX6, PXAAA1, PAF2, PBD4A, PDB4B, HMLR2"	Peroxisomal biogenesis factor 6 (peroxisomal AAA-type ATPase 1)	PEX6	5190	ENSG00000124587		"Heimler syndrome 2, 616617 (3), Autosomal recessive; Peroxisome biogenesis disorder 4A (Zellweger), 614862 (3), Autosomal recessive; Peroxisome biogenesis disorder 4B, 614863 (3), Autosomal recessive, Autosomal dominant"	Pex6 (MGI:2385054)			
chr6	42980343	43017085	6p23-q12	6p21.1		143170	"MEA1, MEA"	Male-enhanced antigen 1	MEA1	4201	ENSG00000124733			Mea1 (MGI:96957)			
chr6	42984498	43012344	6p21.1	6p21.1		601646	"PPP2R5D, MRD35"	"Protein phosphatase-2, regulatory subunit B (B56), delta isoform"	PPP2R5D	5528	ENSG00000112640		"Mental retardation, autosomal dominant 35, 616355 (3), Autosomal dominant"	Ppp2r5d (MGI:2388481)			
chr6	43014102	43021297	6p21.1	6p21.1		611248	"KLHDC3, PEAS"	KELCH domain-containing protein 3	KLHDC3	116138	ENSG00000124702			Klhdc3 (MGI:2651568)			
chr6	43021601	43029598	6p21.1	6p21.1		613475	"RRP36, C6orf153"	"Ribosomal RNA-processing factor, 36"	RRP36	88745	ENSG00000124541			Rrp36 (MGI:2385053)			
chr6	43037616	43053944	6p21.1	6p21.1		609577	"CUL7, 3M1"	Cullin 7	CUL7	9820	ENSG00000044090		"3-M syndrome 1, 273750 (3), Autosomal recessive"	Cul7 (MGI:1913765)			
chr6	43054028	43060179	6p21.3	6p21.1		611822	MRPL2	Mitochondrial ribosomal protein L2	MRPL2	51069	ENSG00000112651			Mrpl2 (MGI:1351622)			
chr6	43076267	43161719	6p21.1-p12.2	6p21.1		601890	PTK7	PTK7 protein tyrosine kinase 7	PTK7	5754	ENSG00000112655			Ptk7 (MGI:1918711)			
chr6	43171294	43181505	6p21.1	6p21.1		600589	SRF	Serum response factor	SRF	6722	ENSG00000112658			Srf (MGI:106658)			
chr6	43182169	43224586	6p21.1	6p21.1		607489	"CUL9, PARC, KIAA0708"	Cullin 9	CUL9	23113	ENSG00000112659			Cul9 (MGI:1925559)			
chr6	43295709	43305537	6p21.2-p21.1	6p21.1		604995	"SLC22A7, OAT2"	"Solute carrier family 22 (organic anion transporter), member 7"	SLC22A7	10864	ENSG00000137204			Slc22a7 (MGI:1859559)			
chr6	43336069	43369442	6p21.1	6p21.1		617512	"ZNF318, TZF, ZFP318"	Zinc finger protein 318	ZNF318	24149	ENSG00000171467			Zfp318 (MGI:1889348)			
chr6	43427537	43451993	6p21.1	6p21.1		612509	"ABCC10, MRP7"	"ATP-binding cassette, subfamily C, member 10"	ABCC10	89845	ENSG00000124574			Abcc10 (MGI:2386976)			
chr6	43477522	43506555	6p21.1	6p21.1		612658	"TJAP1, PILT, TJP4"	Tight junction-associated protein 1	TJAP1	93643	ENSG00000137221			Tjap1 (MGI:1921344)			
chr6	43511826	43516989	6p21.2-p21.1	6p21.1		609775	"YIPF3, KLIP1"	"YIP1 domain family, member 3"	YIPF3	25844	ENSG00000137207			Yipf3 (MGI:106280)			
chr6	43517023	43562403	6p22.3	6p21.1		610060	"POLR1C, RPA39, RPA40, RPAC1, RPA5, TCS3, HLD11"	"Polymerase I, RNA, subunit C"	POLR1C	9533	ENSG00000171453		"Leukodystrophy, hypomyelinating, 11, 616494 (3), Autosomal recessive; Treacher Collins syndrome 3, 248390 (3), Autosomal recessive"	Polr1c (MGI:103288)			
chr6	43522329	43576074	6p21.1	6p21.1		607845	"XPO5, KIAA1291"	Exportin 5	XPO5	57510	ENSG00000124571			Xpo5 (MGI:1913789)			
chr6	43576140	43620522	6p21.1-p12	6p21.1		603968	"POLH, XPV"	"Polymerase, DNA, eta"	POLH	5429	ENSG00000170734		"Xeroderma pigmentosum, variant type, 278750 (3), Autosomal recessive"	Polh (MGI:1891457)			
chr6	43620480	43631308	6p21.2-p21.1	6p21.1		607434	GTPBP2	GTP-binding protein 2	GTPBP2	54676	ENSG00000172432			Gtpbp2 (MGI:1860138)			
chr6	43645029	43671010	6p21.1	6p21.1		612648	"RSPH9, CILD12"	"Radial spoke head 9, Chlamydomonas, homolog of"	RSPH9	221421	ENSG00000172426		"Ciliary dyskinesia, primary, 12, 612650 (3)"	Rsph9 (MGI:1922814)			
chr6	43671196	43687811	6p21.3	6p21.1		611981	"MRPS18A, MRPS18-3"	Mitochondrial ribosomal protein S18A	MRPS18A	55168	ENSG00000096080			Mrps18a (MGI:1915815)			
chr6	43770208	43786486	6p12	6p21.1		192240	"VEGF, MVCD1"	Vascular endothelial growth factor	VEGFA	7422	ENSG00000112715		"{Microvascular complications of diabetes 1}, 603933 (3)"	Vegfa (MGI:103178)			
chr6	44113453	44127490	6p21.3	6p21.1		611827	"MRPL14, MRPL32"	Mitochondrial ribosomal protein L14	MRPL14	64928	ENSG00000180992			Mrpl14 (MGI:1333864)			
chr6	44158810	44184401	6p12	6p21.1		604822	CAPN11	Calpain 11	CAPN11	11131	ENSG00000137225			Capn11 (MGI:1352490)			
chr6	44219504	44234150	6p21.2-p21.1	6p21.1		602193	"SLC29A1, ENT1"	"Solute carrier family 29 (nucleoside transporters), member 1 (equilibrative nucleoside transporter-1)"	SLC29A1	2030	ENSG00000112759			Slc29a1 (MGI:1927073)			
chr6	44246165	44253887	6p21.1	6p21.1		140572	"HSP90AB1, HSPCB, HSPC2, HSP90B"	"Heas-shock protein, 90kD, alpha, class B, member 1"	HSP90AB1	3326	ENSG00000096384			Hsp90ab1 (MGI:96247)			
chr6	44254100	44257889	6p12.1-p11.2	6p21.1		610788	"SLC35B2, PAPST1, SLL"	"Solute carrier family 35 (3'-phosphoadenosine 5')-phosphosulfate transporter), member B2"	SLC35B2	347734	ENSG00000157593			Slc35b2 (MGI:1921086)			
chr6	44258165	44265787	6p21.1	6p21.1		604548	"NFKBIE, IKBE"	"Nuclear factor of kappa light chain gene enhancer in B cells inhibitor, epsilon"	NFKBIE	4794	ENSG00000146232			Nfkbie (MGI:1194908)			
chr6	44280159	44297804	6p21.3-cen	6p21.1		186975	TCTE1	T-complex-associated-testis-expressed-1	TCTE1	202500	ENSG00000146221			Tcte1 (MGI:98640)			
chr6	44297849	44313357	6p21.1	6p21.1		612035	"AARS2, KIAA1270, MTALARS, COXPD8, LKENP"	Alanyl-tRNA synthetase 2	AARS2	57505	ENSG00000124608		"Combined oxidative phosphorylation deficiency 8, 614096 (3), Autosomal recessive; Leukoencephalopathy, progressive, with ovarian failure, 615889 (3), Autosomal recessive"	Aars2 (MGI:2681839)			
chr6	44387513	44450423	6p21	6p21.1		602868	CDC5L	"Cell division cycle 5, S. pombe, homolog-like"	CDC5L	988	ENSG00000096401			Cdc5l (MGI:1918952)			
chr6	44809056	45378050	6p21.1	6p21.1		602947	"SUPT3H, SPT3"	"Suppressor of Ty 3, S. cerevisiae, homolog of"	SUPT3H	8464	ENSG00000196284			Supt3 (MGI:1923723)			
chr6	45328316	45551081	6p21	6p21.1		600211	"RUNX2, CBFA1, PEBP2A1, AML3, CCD, CLCD"	Runt-related transcription factor 2	RUNX2	860	ENSG00000124813		"Cleidocranial dysplasia, 119600 (3), Autosomal dominant; Cleidocranial dysplasia, forme fruste, dental anomalies only, 119600 (3), Autosomal dominant; Cleidocranial dysplasia, forme fruste, with brachydactyly, 119600 (3), Autosomal dominant; Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly, 156510 (3), Autosomal dominant"	Runx2 (MGI:99829)			
chr6	45898450	46129808	6p21.1-p12.1	6p21.1		607293	"CLIC5, DFNB103"	Chloride intracellular channel 5	CLIC5	53405	ENSG00000112782	mutation identified in 1 DFNB103 family	"?Deafness, autosomal recessive 103, 616042 (3), Autosomal recessive"	Clic5 (MGI:1917912)			
chr6	46129963	46146698	6p21.1	6p21.1		617000	"ENPP4, NPP4, KIAA0879"	Ectonucleotide pyrophosphatase/phosphodiesterase 4	ENPP4	22875	ENSG00000001561			Enpp4 (MGI:2682634)			
chr6	46159181	46171009	6p21.1	6p21.1		617001	"ENPP5, NPP5"	Ectonucleotide pyrophosphatase/phosphodiesterase 5	ENPP5	59084	ENSG00000112796			Enpp5 (MGI:1933830)			
chr6	46200000	69200000	6p12-q12			609026	"CTRCT28, ARCC1"	Cataract 28		493862			"{Cataract 28, age-related cortical, susceptibility to}, 609026 (2)"				
chr6	46200000	57200000	6p12			164100	"NYS2, NYSA"	"Nystagmus 2, congenital, autosomal dominant"	NYS2	4933			"Nystagmus 2, congenital, autosomal dominant, 164100 (2), Autosomal dominant"				
chr6	46220729	46492066	6p12.3	6p12.3		604876	"RCAN2, ZAKI4, DSCR1L1, MCIP2, CSP2"	Regulator of calcineurin 2	RCAN2	10231	ENSG00000172348			Rcan2 (MGI:1858219)			
chr6	46549579	46652848	6p21.1-p11.2	6p12.3		605994	CYP39A1	"Cytochrome P450, subfamily XXXIXA (oxysterol 7-alpha-hydroxylase), polypeptide 1"	CYP39A1	51302	ENSG00000146233			Cyp39a1 (MGI:1927096)			
chr6	46652914	46678189	6p12.3	6p12.3		613725	"SLC25A27, UCP4"	"Solute carrier family 25, member 17"	SLC25A27	9481	ENSG00000153291			Slc25a27 (MGI:1921261)			
chr6	46680267	46704318	6p12.3	6p12.3		611200	TDRD6	TUDOR domain-containing protein 6	TDRD6	221400	ENSG00000180113			Tdrd6 (MGI:2679727)			
chr6	46700557	46735835	6p21.2-p12	6p12.3		601690	"PLA2G7, PAFAH, PAFAD"	"Phospholipase A2, group VII (platelet-activating factor acetylhydrolase)"	PLA2G7	7941	ENSG00000146070		"{Asthma, susceptibility to}, 600807 (3), Autosomal dominant; {Atopy, susceptibility to}, 147050 (3), Autosomal dominant; Platelet-activating factor acetylhydrolase deficiency, 614278 (3), Autosomal recessive"	Pla2g7 (MGI:1351327)			
chr6	46793356	46845986	6p21.2-p21.1	6p12.3		600388	MEP1A	"Meprin A, alpha"	MEP1A	4224	ENSG00000112818			Mep1a (MGI:96963)			
chr6	46997702	47042362	6p12.3	6p12.3		617430	"ADGRF1, GPR110"	Adhesion G protein-coupled receptor F1	ADGRF1	266977	ENSG00000153292			Adgrf1 (MGI:1924846)			
chr6	47477745	47627262	6p12	6p12.3		604241	"CD2AP, CMS"	CD2-associated protein	CD2AP	23607	ENSG00000198087		"Glomerulosclerosis, focal segmental, 3, 607832 (3)"	Cd2ap (MGI:1330281)			
chr6	47698544	47722020	6p12.3	6p12.3		614268	"ADGRF4, GPR115"	Adhesion G protein-coupled receptor F4	ADGRF4	221393	ENSG00000153294			Adgrf4 (MGI:1925499)			
chr6	47782036	47831087	6p12.3	6p12.3		609042	"OPN5, GRP136, PGR12"	Opsin 5	OPN5	221391	ENSG00000124818			Opn5 (MGI:2662912)			
chr6	47858597	48111131	6p21.3	6p12.3		616908	"PTCHD4, PTCH53, C6orf138"	Patched domain-containing protein 4	PTCHD4	442213	ENSG00000244694			Ptchd4 (MGI:1920485)			
chr6	49430359	49463327	6p21	6p12.3		609058	"MUT, MCM"	Methylmalonyl Coenzyme A mutase	MUT	4594	ENSG00000146085		"Methylmalonic aciduria, mut(0) type, 251000 (3), Autosomal recessive"	Mut (MGI:97239)			
chr6	49463326	49493106	6p12.3	6p12.3		611506	CENPQ	Centromeric protein Q	CENPQ	55166	ENSG00000031691			Cenpq (MGI:1933744)			
chr6	49499957	49528063	6p12.3	6p12.3		614763	GLYATL3	Glycine N-acyltransferase-like 3	GLYATL3	389396	ENSG00000203972			Glyatl3 (MGI:3647683)			
chr6	49605174	49636873	6p21.1-p11	6p12.3		180297	"RHAG, RH50A, OHST"	Rhesus blood group-associated glycoprotein	RHAG	6005	ENSG00000112077		"Anemia, hemolytic, Rh-null, regulator type, 268150 (3), Autosomal dominant; Overhydrated hereditary stomatocytosis, 185000 (3), Autosomal dominant; Rh-mod syndrome (3)"	Rhag (MGI:1202713)			
chr6	49676664	49714197	6p12	6p12.3		187430	"CRISP2, TPX1, TSP1"	Cysteine-rich secretory protein 2	CRISP2	7180	ENSG00000124490			Crisp2 (MGI:98815)			
chr6	49785650	49787339	6p21.1-p12	6p12.3		172270	PGK2	Phosphoglycerate kinase-2 (testicular PGK)	PGK2	5232	ENSG00000170950	pseudogene on chr.12		Pgk2 (MGI:97563)			
chr6	49833938	49877095	6p21.2-p21.1	6p12.3		601193	"CRISP1, AEGL1"	Cysteine-rich secretory protein 1	CRISP1	167	ENSG00000124812			Crisp4 (MGI:1925331)			
chr6	49960291	49964104	6p12	6p12.3		615243	"DEFB114, DEFB14"	"Defensin, beta, 114"	DEFB114	245928	ENSG00000177684						
chr6	50713543	50773032	6p21.1-p12.1	6p12.3		610161	"TFAP2D, TFAP2BL1"	Transcription factor AP2-delta	TFAP2D	83741	ENSG00000008197			Tfap2d (MGI:2153466)			
chr6	50817691	50847618	6p12	6p12.3		601601	"TFAP2B, CHAR, PDA2"	Transcription factor AP-2 beta (activating enhancer-binding protein 2 beta)	TFAP2B	7021	ENSG00000008196		"Char syndrome, 169100 (3), Autosomal dominant; Patent ductus arteriosus 2, 617035 (3), Autosomal dominant"	Tfap2b (MGI:104672)			
chr6	51614684	52087624	6p12.3-p12.2	6p12.3-p12.2		606702	"FCYT, PKHD1, ARPKD, PKD4"	Fibrocystin	PKHD1	5314	ENSG00000170927		"Polycystic kidney disease 4, with or without hepatic disease, 263200 (3), Autosomal recessive"	Pkhd1 (MGI:2155808)			
chr6	51800000	69200000	6p12.2-q12			614345	MRT24	"Mental retardation, autosomal recessive 24"	MRT24	100852402		between rs651733 and rs1508668	"Mental retardation, autosomal recessive 24, 614345 (2), Autosomal recessive"				
chr6	52144348	52144433	6p12.2	6p12.2		611599	"MIR206, MIRN206"	Micro RNA 206	MIR206	406989							
chr6	52146813	52151022	6p12.2	6p12.2		614933	LINCMD1	"Long intergenic noncoding RNA, muscle differentiation 1"	LINCMD1	101154644							
chr6	52148922	52149040	6p12.2	6p12.2		610946	"MIR133B, MIRN133B"	Micro RNA 133B	MIR133B	442890							
chr6	52186386	52190637	6p12.2	6p12.2		603149	"IL17A, IL17, CTLA8"	Interleukin-17a	IL17A	3605	ENSG00000112115	previously mapped to 2q31		Il17a (MGI:107364)			
chr6	52236680	52245688	6p12	6p12.2		606496	"IL17F, ML1, CANDF6"	Interleukin 17F	IL17F	112744	ENSG00000112116	mutation identified in 1 CANDF6 family	"?Candidiasis, familial, 6, autosomal dominant, 613956 (3)"	Il17f (MGI:2676631)			
chr6	52264013	52284880	6p12	6p12.2		602693	MCM3	"Minichromosome maintenance, S. cerevisiae, homolog of, 3"	MCM3	4172	ENSG00000112118			Mcm3 (MGI:101845)			
chr6	52362127	52407776	6p12	6p12.2		607780	"PAQR8, C6orf33, LMPB1, MPRB"	"Progestin and ADIPOQ receptor family, member 8"	PAQR8	85315	ENSG00000170915			Paqr8 (MGI:1921479)			
chr6	52420195	52495784	6p12-p11	6p12.2		608815	"EFHC1, FLJ10466, EJM1, JAE, EJA1"	EF hand domain (C-terminal)-containing 1	EFHC1	114327	ENSG00000096093		"{Epilepsy, juvenile absence, susceptibility to, 1}, 607631 (3), Autosomal dominant; {Myoclonic epilepsy, juvenile, susceptibility to, 1}, 254770 (3), Autosomal dominant"	Efhc1 (MGI:1919127)			
chr6	52497401	52577063	6p12.2	6p12.2		608485	"TRAM2, KIAA0057"	Translocation-associated membrane protein 2	TRAM2	9697	ENSG00000065308			Tram2 (MGI:1924817)			
chr6	52671085	52686587	6p12.2	6p12.2		616870	TMEM14A	Transmembrane protein 14A	TMEM14A	28978	ENSG00000096092			Tmem14a (MGI:1922962)			
chr6	52750086	52763562	6p12.2	6p12.2		138360	"GSTA2, GST2"	Glutathione S-transferase A2	GSTA2	2939	ENSG00000244067						
chr6	52791379	52803966	6p12.2	6p12.2		138359	GSTA1	Glutathione S-transferase A1	GSTA1	2938	ENSG00000243955						
chr6	52831741	52846094	6p12.2	6p12.2		607605	GSTA5	"Glutathione S-transferase, alpha-5"	GSTA5	221357	ENSG00000182793			"Gm10639,Gsta1,Gsta2,Gm3776 (MGI:1095417,MGI:3704339,MGI:95863,MGI:3826440)"			
chr6	52896638	52909798	6p12.2	6p12.2		605449	GSTA3	"Glutathione S-transferase, alpha-3"	GSTA3	2940	ENSG00000174156			Gsta3 (MGI:95856)			
chr6	52977947	52995379	6p12.2	6p12.2		605450	GSTA4	"Glutathione S-transferase, alpha-4"	GSTA4	2941	ENSG00000170899						
chr6	52995619	52995950	6p12.1	6p12.2		606515	"RN7SK, 7SK"	"RNA, 7SK small nuclear"	RN7SK	125050							
chr6	53001298	53061863	6p12.3	6p12.1		612325	"ICK, MRK, KIAA0936, ECO, EJM10"	Intestinal cell kinase	ICK	22858	ENSG00000112144		"Endocrine-cerebroosteodysplasia, 612651 (3), Autosomal recessive; {Epilepsy, juvenile myoclonic, susceptibility to, 10}, 617924 (3)"	Ick (MGI:1934157)			
chr6	53057806	53100872	6p12.3-p11.2	6p12.1		609091	"FBXO9, FBX9"	F-box only protein 9	FBXO9	26268	ENSG00000112146			Fbxo9 (MGI:1918788)			
chr6	53126960	53262802	6p12.1	6p12.1		603715	"GCM1, GCMA"	"Glial cells missing, Drosophila, homolog of, 1"	GCM1	8521	ENSG00000137270			Gcm1 (MGI:108045)			
chr6	53267397	53349178	6p12	6p12.1		611805	"ELOVL5, HELO1, SCA38"	Elongation of very long chain fatty acids-like 5	ELOVL5	60481	ENSG00000012660		"Spinocerebellar ataxia 38, 615957 (3), Autosomal dominant"	Elovl5 (MGI:1916051)			
chr6	53497340	53545128	6p12	6p12.1		606857	"GCLC, GLCLC"	"Glutamate-cysteine ligase, catalytic subunit"	GCLC	2729	ENSG00000001084		"Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency, 230450 (3), Autosomal recessive; {Myocardial infarction, susceptibility to}, 608446 (3)"	Gclc (MGI:104990)			
chr6	53647900	53665853	6p12	6p12.1		610749	"KLHL31, KLHL"	Kelch-like 31	KLHL31	401265	ENSG00000124743			Klhl31 (MGI:3045305)			
chr6	53794496	53924124	6p12.3-p12.2	6p12.1		608195	"LRRC1, LANO"	Leucine-rich repeat-containing protein 1	LRRC1	55227	ENSG00000137269			Lrrc1 (MGI:2442313)			
chr6	54018915	54266324	6p12.1	6p12.1		614106	"MLIP, C6orf142"	Muscular LMNA-interating protein	MLIP	90523	ENSG00000146147			Mlip (MGI:1916892)			
chr6	54307791	54390151	6p12-p11.2	6p12.1		606749	"TINAG, TIN1, TIN2"	Tubulointerstitial nephritis antigen	TINAG	27283	ENSG00000137251			Tinag (MGI:1349477)			
chr6	55106459	55284697	6p12.1	6p12.1		602393	"HCRTR2, OX2R"	Hypocretin receptor 2	HCRTR2	3062	ENSG00000137252			Hcrtr2 (MGI:2680765)			
chr6	55327468	55402492	6p12.1	6p12.1		617837	"GFRAL, GRAL"	GDNF family receptor alpha-like protein	GFRAL	389400	ENSG00000187871			Gfral (MGI:3607786)			
chr6	55753652	55875589	6p12.1	6p12.1		112265	BMP5	Bone morphogenetic protein-5	BMP5	653	ENSG00000112175			Bmp5 (MGI:88181)			
chr6	56056589	56394127	6p12.3-p11.2	6p12.1		610002	COL21A1	"Collagen, type XXI, alpha-1 polypeptide"	COL21A1	81578	ENSG00000124749						
chr6	56457986	56954670	6p12-p11	6p12.1		113810	"DST, BPAG1, DMH, D6S1101, HSAN6, EBSB2"	Dystonin (bullous pemphigoid antigen 1)	DST	667	ENSG00000151914	?mutation identified in 1 HSAN6 family	"Epidermolysis bullosa simplex, autosomal recessive 2, 615425 (3), Autosomal recessive; ?Neuropathy, hereditary sensory and autonomic, type VI, 614653 (3), Autosomal recessive"				
chr6	57088969	57170304	6p12.1	6p12.1		615708	"ZNF451, COASTER"	Zinc finger protein 451	ZNF451	26036	ENSG00000112200			Zfp451 (MGI:2137896)			
chr6	57172305	57185214	6p11.2	6p12.1		603882	BAG2	BCL2-associated athanogene 2	BAG2	9532	ENSG00000112208			Bag2 (MGI:1891254)			
chr6	57186991	57222313	6p11	6p12.1-p11.2		606144	RAB23	Ras-associated protein RAB23	RAB23	51715	ENSG00000112210		"Carpenter syndrome, 201000 (3), Autosomal recessive"	Rab23 (MGI:99833)			
chr6	57200000	59800000	6p11			608173	AITD1	"Autoimmune thyroid disease, susceptibility to, 1"		387578			"{Autoimmune thyroid disease, susceptibility to, 1}, 608173 (2)"				
chr6	57314804	57646851	6p12-p11.1	6p11.2		176636	PRIM2A	"Primase polypeptide 2A, 58kD"	PRIM2	5558	ENSG00000146143			Prim2 (MGI:97758)			
chr6	59800000	170805979	6q			193007	BPPV	"Vertigo, benign paroxysmal positional"		619536		max lod at D6S1556	"Vestibulopathy, familial, 193007 (2), Autosomal dominant"				
chr6	59800000	87300000	6q11-q14			613544	"DEL6q11q14, C6DELq11q14"	Chromosome 6q11-q14 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 6q11-q14 deletion syndrome, 613544 (4), Isolated cases"				
chr6	61542696	62286226	6q11.1	6q11.1		610487	"KHDRBS2, SLM1"	"KH domain-containing, RNA-binding, signal transduction-associated protein 2"	KHDRBS2	202559	ENSG00000112232			Khdrbs2 (MGI:2159649)			
chr6	62700000	69200000	6q12			608905	ADHD3	"Attention deficit-hyperactivity disorder, susceptibility to, 2"		450089			"{Attention deficit-hyperactivity disorder}, 143465 (2), Autosomal dominant"				
chr6	62700000	105000000	6q12-q16			605582	CMD1K	"Cardiomyopathy, dilated, 1K"	CMD1K	65014			"Cardiomyopathy, dilated, 1K, 605582 (2)"				
chr6	62700000	92500000	6q12-q15			614342	MRT30	"Mental retardation, autosomal recessive 30"		100852401		between rs4612125 and rs285651	"Mental retardation, autosomal recessive 30, 614342 (2), Autosomal recessive"				
chr6	63528020	63583587	6q12	6q12		601585	"PTP4A1, HH72, PRL1"	"Protein tyrosine phosphatase, type 4A, 1"	PTP4A1	7803	ENSG00000112245			Ptp4a1 (MGI:1277096)			
chr6	63635801	63715521	6q12	6q12		607789	"PHF3, KIAA0244"	PHD finger protein 3	PHF3	23469	ENSG00000118482			Phf3 (MGI:2446126)			
chr6	63719979	65707224	6q12	6q12		612424	"EYS, RP25"	"Eyes shut, Drosophila, homolog of"	EYS	346007	ENSG00000188107		"Retinitis pigmentosa 25, 602772 (3), Autosomal recessive"				
chr6	68635282	69389510	6q12	6q12-q13		602684	"ADGRB3, BAI3"	Adhesion G protein-coupled receptor B3	ADGRB3	577	ENSG00000135298			Adgrb3 (MGI:2441837)			
chr6	69200000	98900000	6q13-q16.1			611572	OTSC7	Otosclerosis 7	OTSC7	399516		between D6S1036 and D6S300	"Otosclerosis 7, 611572 (2), Autosomal dominant"				
chr6	69200000	164100000	6q13-q26			603175	SCZD5	"Schizophrenia susceptibility locus, chromosome 6q-related"				max lod at D6S1626 and D6S292	"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr6	69675748	69797156	6q13	6q13		612625	"LMBRD1, LMBD1, NESI, MAHCF"	LMBR1 domain-containing protein 1	LMBRD1	55788	ENSG00000168216		"Methylmalonic aciduria and homocystinuria, cblF type, 277380 (3), Autosomal recessive"	Lmbrd1 (MGI:1915671)			
chr6	69866555	70215062	6q12-q14	6q13		120165	"COL19A1, D6S228E, COL9A1L"	"Collagen XIX, alpha-1 polypeptide"	COL19A1	1310	ENSG00000082293			Col19a1 (MGI:1095415)			
chr6	70216039	70303082	6q13	6q13		120210	"COL9A1, EDM6, STL4"	"Collagen IX, alpha-1 polypeptide"	COL9A1	1297	ENSG00000112280	mutation identified in 1 EDM6 family	"?Epiphyseal dysplasia, multiple, 6, 614135 (3), Autosomal dominant; Stickler syndrome, type IV, 614134 (3)"	Col9a1 (MGI:88465)			
chr6	70667770	70862014	6q13	6q13		611372	SMAP1	Small ADP-ribosylation factor GTPase-activating protein 1	SMAP1	60682	ENSG00000112305			Smap1 (MGI:2138261)			
chr6	70861365	70957084	6q13	6q13		607497	"GLCATS, KIAA1963"	UDP-glucuronyltransferase S	B3GAT2	135152	ENSG00000112309			B3gat2 (MGI:2389490)			
chr6	71403550	71403620	6q13	6q13		612329	"MIR30A, MIRN30A"	Micro RNA 30A	MIR30A	407029							
chr6	71886702	72403142	6q12-q13	6q13		606629	"RIMS1, RIM1, RIM, KIAA0340, CORD7"	Regulating synaptic membrane exocytosis 1	RIMS1	22999	ENSG00000079841		"Cone-rod dystrophy 7, 603649 (3)"	Rims1 (MGI:2152971)			
chr6	72621842	73198850	6q14	6q13		607357	"KCNQ5, MRD46"	"Potassium channel, voltage-gated, KQT-like subfamily, member 5"	KCNQ5	56479	ENSG00000185760		"Mental retardation, autosomal dominant 46, 617601 (3), Autosomal dominant"	Kcnq5 (MGI:1924937)			
chr6	73241313	73310364	6q13	6q13		611688	KHDC1	KH homology domain-containing protein 1	KHDC1	80759	ENSG00000135314						
chr6	73353061	73354275	6q13	6q13		611111	"DPPA5, ESG1"	Developmental pluripotency-associated gene 5	DPPA5	340168	ENSG00000203909			Dppa5a (MGI:101800)			
chr6	73362676	73364174	6q13	6q13		611687	"KHDC3L, C6orf221, ECAT1, HYDM2"	"KH domain containing 3-like, subcortical maternal complex member"	KHDC3L	154288	ENSG00000203908		"Hydatidiform mole, recurrent, 2, 614293 (3), Autosomal recessive"	Khdc3 (MGI:1914241)			
chr6	73368554	73369791	6q13	6q13		611689	"OOEP, KHDC2"	"Oocyte-expressed protein, Dog, homolog of"	OOEP	441161	ENSG00000203907			Ooep (MGI:1915218)			
chr6	73394561	73417565	6q12-q13	6q13		606286	"DDX43, HAGE"	DEAD/H box 43	DDX43	55510	ENSG00000080007			Ddx43 (MGI:3642857)			
chr6	73425132	73452319	6q13	6q13		613973	"CGAS, MB21D1, C6orf150"	Cyclic GMP-AMP synthase	CGAS	115004	ENSG00000164430			Mb21d1 (MGI:2442261)			
chr6	73461730	73501455	6q13	6q13		614667	"MTO1, COXPD10"	"Mitochondrial translation optimization 1, S. cerevisiae, homolog of"	MTO1	25821	ENSG00000135297		"Combined oxidative phosphorylation deficiency 10, 614702 (3), Autosomal recessive"	Mto1 (MGI:1915541)			
chr6	73515749	73521031	6q14	6q13		130590	"EEF1A1, EF1A"	"Eukaryotic translation elongation factor-1, alpha-1"	EEF1A1	1915	ENSG00000156508			Eef1a1 (MGI:1096881)			
chr6	73593378	73654013	6q14-q15	6q13		604322	"SLC17A5, SIASD, SLD"	"Solute carrier family 17 (sodium phosphate), member 5"	SLC17A5	26503	ENSG00000119899		"Salla disease, 604369 (3), Autosomal recessive; Sialic acid storage disorder, infantile, 269920 (3), Autosomal recessive"	Slc17a5 (MGI:1924105)			
chr6	73696084	73828316	6q13	6q13		608859	CD109	CD109 antigen	CD109	135228	ENSG00000156535			Cd109 (MGI:2445221)			
chr6	75084325	75206261	6q13-q14.1	6q13-q14		120320	"COL12A1, UCMD2, BTHLM2, EDSMYP"	"Collagen, type XII, alpha-1"	COL12A1	1303	ENSG00000111799	mutation identified in 1 UCMD2 family	"Bethlem myopathy 2, 616471 (3), Autosomal dominant; ?Ullrich congenital muscular dystrophy 2, 616470 (3)"	Col12a1 (MGI:88448)			
chr6	75200000	105000000	6q14-q16			608988	ATFB2	"Atrial fibrillation, familial, 2"		619478		max lod between  D6S286 and D6S1021	"Atrial fibrillation, familial, 2, 608988 (2)"				
chr6	75200000	100000000	6q14-q16.2			600790	"PBCRA, CRAPB"	Progressive bifocal chorioretinal atrophy	PBCRA1	7948			"Chorioretinal atrophy, progressive bifocal, 600790 (2), Autosomal dominant"				
chr6	75200000	83200000	6q14.1			610685	SHFLD2	Split-hand/foot malformation with long bone deficiency 2		791123		between rs623155 and rs1547251	"Split-hand/foot malformation with long bone deficiency 2, 610685 (2)"				
chr6	75237674	75244658	6q12	6q14.1		123996	COX7A2	"Cytochrome c oxidase, subunit VIIa, polypeptide-2, liver"	COX7A2	1347	ENSG00000112695	previously thought to be on chr.4		Cox7a2 (MGI:1316715)			
chr6	75252921	75284915	6q14.1	6q14.1		611028	"TMEM30A, CDC50A"	Transmembrane protein 30A	TMEM30A	55754	ENSG00000112697			Tmem30a (MGI:106402)			
chr6	75291857	75493913	6q14.1	6q14.1		607307	"FILIP, KIAA1275"	Filamin A-interacting protein	FILIP1	27145	ENSG00000118407			Filip1 (MGI:1917848)			
chr6	75601508	75718284	6q13	6q14.1		605003	"SENP6, SSP1, SUSP1"	"Sentrin-specific protease family, member 6"	SENP6	26054	ENSG00000112701			Senp6 (MGI:1922075)			
chr6	75749175	75919536	6q13	6q14.1		600970	"MYO6, DFNA22, DFNB37"	Myosin VI	MYO6	4646	ENSG00000196586		"Deafness, autosomal dominant 22, 606346 (3), Autosomal dominant; Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, 606346 (3), Autosomal dominant; Deafness, autosomal recessive 37, 607821 (3), Autosomal recessive"	Myo6 (MGI:104785)			
chr6	75921113	76072677	6q13-q15	6q14.1		602870	"IMPG1, IPM150, VMD4"	Interphotoreceptor matrix proteoglycan-1	IMPG1	3617	ENSG00000112706		"Macular dystrophy, vitelliform, 4, 616151 (3), Autosomal dominant"	Impg1 (MGI:1926876)			
chr6	77460847	77464021	6q13	6q14.1		182131	HTR1B	5-hydroxytryptamine (serotonin) receptor-1B	HTR1B	3351	ENSG00000135312			Htr1b (MGI:96274)			
chr6	78867485	78979410	6q14.1	6q14.1		615375	"IRAK1BP1, SIMPL"	Interleukin 1 receptor-associated kinase 1-binding protein 1	IRAK1BP1	134728	ENSG00000146243			Irak1bp1 (MGI:1929475)			
chr6	78934418	79078297	6q14	6q14.1		612870	PHIP	Pleckstrin homology domain-interacting protein	PHIP	55023	ENSG00000146247			Phip (MGI:1932404)			
chr6	79201244	79234737	6q14.1	6q14.1		604502	"HMGN3, TRIP7"	High-mobility group nucleosomal binding protein 3 (thyroid hormone receptor interactor 7)	HMGN3	9324	ENSG00000118418						
chr6	79484990	79537429	6q14.1	6q14.1		611408	"LCA5, C6orf152"	Lebercilin	LCA5	167691	ENSG00000135338		"Leber congenital amaurosis 5, 604537 (3)"	Lca5 (MGI:1923032)			
chr6	79631104	79703669	6q14.1	6q14.1		615678	SH3BGRL2	SH3 domain-binding glutamic acid-rich protein-like protein 2	SH3BGRL2	83699	ENSG00000198478			Sh3bgrl2 (MGI:1915350)			
chr6	79914811	79947597	6q14	6q14.1		605512	"ELOVL4, ADMD, STGD2, STGD3, ISQMR, SCA34"	Elongation of very long chain fatty acids 4	ELOVL4	6785	ENSG00000118402		"Ichthyosis, spastic quadriplegia, and mental retardation, 614457 (3), Autosomal recessive; Spinocerebellar ataxia 34, 133190 (3), Autosomal dominant; Stargardt disease 3, 600110 (3), Autosomal dominant"	Elovl4 (MGI:1933331)			
chr6	80004146	80042650	6q13-q21	6q14.1		604092	"TTK, MPS1L1, PYT"	TTK protein kinase	TTK	7272	ENSG00000112742			Ttk (MGI:1194921)			
chr6	80106609	80469087	6q14	6q14.1		248611	"BCKDHB, E1B"	"Branched chain keto acid dehydrogenase E1, beta polypeptide"	BCKDHB	594	ENSG00000083123		"Maple syrup urine disease, type Ib, 248600 (3), Autosomal recessive"	Bckdhb (MGI:88137)			
chr6	82169986	82247753	6q13-q14	6q14.1		606457	IBTK	Inhibitor of Bruton agammaglobulinemia tyrosine kinase	IBTK	25998	ENSG00000005700			Ibtk (MGI:1918677)			
chr6	82363205	82367416	6q14-q15	6q14.1		190920	TPBG	Trophoblast glycoprotein	TPBG	7162	ENSG00000146242			Tpbg (MGI:1341264)			
chr6	82880833	83065840	6q14.1	6q14.1		612495	"UBE2CBP, H10BH"	Ubiquitin-conjugating enzyme E2C-binding protein	UBE3D	90025	ENSG00000118420			Ube2cbp (MGI:1917598)			
chr6	83067665	83171350	6q14.1	6q14.1		616823	"DOPEY1, DOP1, KIAA1117"	DOPEY family member 1	DOPEY1	23033	ENSG00000083097			Dopey1 (MGI:1289294)			
chr6	83150727	83193935	6q12	6q14.1		172100	"PGM3, AGM1, IMD23"	Phosphoglucomutase-3 (N-acetylglucosamine-phosphate mutase 1)	PGM3	5238	ENSG00000013375		"Immunodeficiency 23, 615816 (3), Autosomal recessive"	Pgm3 (MGI:97566)			
chr6	83210388	83431218	6q12	6q14.2		154250	ME1	"Malic enzyme, cytoplasmic"	ME1	4199	ENSG00000065833			Me1 (MGI:97043)			
chr6	83552884	83709407	6q14.2	6q14.2		607923	"SNAP91, AP180, KIAA0656"	"Synaptosomal-associated protein, 91kD"	SNAP91	9892	ENSG00000065609			Snap91 (MGI:109132)			
chr6	83853265	83857514	6q14.2	6q14.2		609891	"RIPPLY2, C6orf59, SCDO6"	"Ripply2, zebrafish, homolog of"	RIPPLY2	134701	ENSG00000203877	mutation identified in 1 SCDO6 family	"?Spondylocostal dysostosis 6, 616566 (3), Autosomal recessive"	Ripply2 (MGI:2685968)			
chr6	83859650	83960426	6q14-q15	6q14.2		608343	"CYB5R4, NCB5OR"	Cytochrome b5 reductase 4	CYB5R4	51167	ENSG00000065615			Cyb5r4 (MGI:2386848)			
chr6	84032620	84146277	6q14.2	6q14.2		615410	"MRAP2, C6orf117, BMIQ18"	Melanocortin 2 receptor accessory protein 2	MRAP2	112609	ENSG00000135324	mutation identified in 1 BMIQ18 individual	"{?Obesity, susceptibility to, BMIQ18}, 615457 (3), Autosomal dominant"	Mrap2 (MGI:3609239)			
chr6	84124240	84227888	6q14.2-q14.3	6q14.2-q14.3		610201	"CEP162, KIAA1009"	"Centrosomal protein, 162kD"	CEP162	22832	ENSG00000135315			Cep162 (MGI:1925343)			
chr6	84666809	84764235	6q14.3	6q14.3		604613	"TBX18, CAKUT2"	T-box 18	TBX18	9096	ENSG00000112837		"Congenital anomalies of kidney and urinary tract 2, 143400 (3), Autosomal dominant"	Tbx18 (MGI:1923615)			
chr6	85449583	85495790	6q14-q21	6q14.3		129190	"NT5E, NT5"	"5' nucleotidase, ecto (CD73)"	NT5E	4907	ENSG00000135318		"Calcification of joints and arteries, 211800 (3), Autosomal recessive"	Nt5e (MGI:99782)			
chr6	85505495	85594155	6q14.3	6q14.3		616105	"SNX14, SCAR20"	Sorting nexin 14	SNX14	57231	ENSG00000135317		"Spinocerebellar ataxia, autosomal recessive 20, 616354 (3), Autosomal recessive"	Snx14 (MGI:2155664)			
chr6	85607783	85643861	6q14.3	6q14.3		616686	"SYNCRIP, NSAP1, GRYRBP, HNRNPQ"	Synaptotagmin-binding cytoplasmic RNA-interacting protein	SYNCRIP	10492	ENSG00000135316			Syncrip (MGI:1891690)			
chr6	85677006	85678732	6q15	6q14.3		613263	"SNHG5, U50HG"	Small nucleolar RNA host gene 5	SNHG5	387066							
chr6	85677293	85677367	6q15	6q14.3		613117	"SNORD50A, RNU50"	"Small nucleolar RNA, C/D box, 50A"	SNORD50A	26799							
chr6	85677588	85677658	6q15	6q14.3		613264	SNORD50B	"Small nucleolar RNA, C/D box"	SNORD50B	692088							
chr6	86936918	87020067	6q14-q15	6q14.3		182132	HTR1E	5-hydroxytryptamine (serotonin) receptor-1E	HTR1E	3354	ENSG00000168830						
chr6	87085497	87095146	6q12-q21	6q14.3		118850	CGA	"Chorionic gonadotropin, alpha polypeptide"	CGA	1081	ENSG00000135346	"shared with LH, FSH, TSH"		Cga (MGI:88390)			
chr6	87155548	87265942	6q14.3	6q14.3		616213	"ZNF292, ZFP292, KIAA0530"	Zinc finger protein 292	ZNF292	23036	ENSG00000188994			Zfp292 (MGI:1353423)			
chr6	87282977	87329277	6q15	6q14-q15		611921	"GJB7, CX25"	"Gap junction protein, beta-7"	GJB7	375519	ENSG00000164411						
chr6	87472924	87512338	6q15	6q15		605634	"SLC35A1, CST, CDG2F"	"Solute carrier family 35 (CMP-sialic acid transporter), member 1"	SLC35A1	10559	ENSG00000164414		"Congenital disorder of glycosylation, type IIf, 603585 (3), Autosomal recessive"	Slc35a1 (MGI:1345622)			
chr6	87513934	87590031	6q16.1	6q15		611524	"RARS2, RARSL, PCH6"	Arginyl-tRNA synthetase 2	RARS2	57038	ENSG00000146282		"Pontocerebellar hypoplasia, type 6, 611523 (3), Autosomal recessive"	Rars2 (MGI:1923596)			
chr6	87590066	87677823	6q15	6q15		604972	"ORC3, ORC3L, LAT"	"Origin recognition complex, subunit 3, S. cerevisiae, homolog of"	ORC3	23595	ENSG00000135336			Orc3 (MGI:1354944)			
chr6	87674859	87702266	6q15	6q15		615165	AKIRIN2	Akirin 2	AKIRIN2	55122	ENSG00000135334			Akirin2 (MGI:1889364)			
chr6	88046906	88066831	6q15-q16.2	6q15		612739	"SPACA1, SAMP32"	Sperm acrosome-associated 1	SPACA1	81833	ENSG00000118434			Spaca1 (MGI:1914902)			
chr6	88139863	88172848	6q14-q15	6q15		114610	CNR1	"Cannabinoid receptor-1, brain"	CNR1	1268	ENSG00000118432			Cnr1 (MGI:104615)			
chr6	88609896	88963628	6q16	6q15		603512	"RNGTT, HCE1, CAP1A"	RNA guanylyltransferase and 5'-phosphatase	RNGTT	8732	ENSG00000111880			Rngtt (MGI:1329041)			
chr6	89080709	89085159	6q15	6q15		606714	"PNRC1, PROL2"	Proline-rich nuclear receptor coactivator 1	PNRC1	10957	ENSG00000146278			Pnrc1 (MGI:1917838)			
chr6	89094817	89165568	6q15	6q15		615913	"PM20D2, ACY1L2"	Peptidase M20 domain-containing 2	PM20D2	135293	ENSG00000146281			Pm20d2 (MGI:2685270)			
chr6	89177503	89231287	6q14-q21	6q15		137161	GABRR1	"Gamma-aminobutyric acid (GABA) A receptor, rho-1"	GABRR1	2569	ENSG00000146276			Gabrr1 (MGI:95625)			
chr6	89254463	89315298	6q14-q21	6q15		137162	GABRR2	"Gamma-aminobutyric acid (GABA) A receptor, rho-2"	GABRR2	2570	ENSG00000111886			Gabrr2 (MGI:95626)			
chr6	89326624	89353154	6q15	6q15		616175	"UBE2J1, UBC6E"	Ubiquitin-conjugating enzyme E2J 1	UBE2J1	51465	ENSG00000198833			Ube2j1 (MGI:1926245)			
chr6	89363508	89412275	6q15-q16	6q15		608268	"RRAGD, RAGD"	RAS-related GTP-binding protein D	RRAGD	58528	ENSG00000025039			Rragd (MGI:1098604)			
chr6	89433177	89633833	6q14-q16	6q15		610583	"ANKRD6, KIAA0957"	Ankyrin repeat domain-containing protein 6	ANKRD6	22881	ENSG00000135299			Ankrd6 (MGI:2154278)			
chr6	89829899	89874435	6q15	6q15		606880	"CASP8AP2, FLASH"	Caspase 8-associated protein 2	CASP8AP2	9994	ENSG00000118412			Casp8ap2 (MGI:1349399)			
chr6	89894468	89896099	6q15	6q15		611924	"GJA10, CX62"	"Gap junction protein, alpha-10"	GJA10	84694	ENSG00000135355			Gja10 (MGI:1339969)			
chr6	89926527	90296907	6q15	6q15		605394	BACH2	BTB and CNC homology 2	BACH2	60468	ENSG00000112182			Bach2 (MGI:894679)			
chr6	90513572	90587300	6q14-q21	6q15		602614	"MAP3K7, TAK1, CSCF, FMD2"	Mitogen-activated protein kinase kinase kinase 7	MAP3K7	6885	ENSG00000135341		"Cardiospondylocarpofacial syndrome, 157800 (3), Autosomal dominant; Frontometaphyseal dysplasia 2, 617137 (3), Autosomal dominant"				
chr6	93240019	93419583	6q16.1	6q16.1		602190	"EPHA7, HEK11"	Ephrin receptor EphA7	EPHA7	2045	ENSG00000135333			Epha7 (MGI:95276)			
chr6	95577496	95609451	6q16	6q16.1		612327	"MANEA, ENDO"	"Mannosidase, endo-alpha"	MANEA	79694	ENSG00000172469			Manea (MGI:2444484)			
chr6	96015968	96215611	6q16	6q16.1		606865	FUT9	Fucosyltransferase 9	FUT9	10690	ENSG00000172461			Fut9 (MGI:1330859)			
chr6	96521825	96555275	6q16.1	6q16.1		613372	"UFL1, KIAA0776, NLBP"	UFM1-specific ligase 1	UFL1	23376	ENSG00000014123			Ufl1 (MGI:1914740)			
chr6	96562524	96618625	6q16.1-q16.3	6q16.1		605126	"FHL5, ACT"	Four-and-a-half LIM domains 5	FHL5	9457	ENSG00000112214			Fhl5 (MGI:1913192)			
chr6	96794121	96837476	6q16.1-q16.3	6q16.1		606915	GPR63	G protein-coupled receptor 63	GPR63	81491	ENSG00000112218			Gpr63 (MGI:2135884)			
chr6	96889310	96897890	6q16.1	6q16.1		611776	"NDUFAF4, HRPAP20, C6orf66"	"NADH dehydrogenase 1 alpha subcomplex, assembly factor 4"	NDUFAF4	29078	ENSG00000123545		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufaf4 (MGI:1915743)			
chr6	97142160	97283436	6q16.1	6q16.1		615614	"MMS22L, C6orf167"	MMS22-like protein	MMS22L	253714	ENSG00000146263			Mms22l (MGI:2684980)			
chr6	98830140	98831699	6q16.1	6q16.1		616328	PNKY	Long intergenic noncoding RNA Pinky		105447646							
chr6	98834703	98838789	6q16	6q16.1		600494	"POU3F2, OCT7"	"POU domain, class 3, transcription factor 2"	POU3F2	5454	ENSG00000184486			Pou3f2 (MGI:101895)			
chr6	98868534	98948005	6q16.1-q16.3	6q16.1-q16.2		605654	"FBXL4, FBL4, MTDPS13"	F-box and leucine-rich repeat protein 4	FBXL4	26235	ENSG00000112234		"Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type), 615471 (3), Autosomal recessive"	Fbxl4 (MGI:2140367)			
chr6	98900000	100000000	6q16.2			616842	"DHS6S1, MCDR1"	"DNase1 hypersensitivity, chromosome 6, site 1"		107305681		upstream of PRDM13 and CCNC	"Macular dystrophy, North Carolina type, 136550 (3), Autosomal dominant"				
chr6	98900000	117900000	6q16.2-q22.1			611944	LMPH1B	"Lymphedema, hereditary, IB"		100188865		max lod at D6S1671	"Lymphedema, hereditary, IB, 611944 (2), Autosomal dominant"				
chr6	99398050	99426305	6q16.2	6q16.2		616653	"PNISR, SRRP130, SFRS18"	PNN-interacting serine/arginine-rich protein	PNISR	25957	ENSG00000132424			Pnisr (MGI:1913875)			
chr6	99542386	99568813	6q21	6q16.2		123838	CCNC	Cyclin C	CCNC	892	ENSG00000112237			Ccnc (MGI:1858199)			
chr6	99606773	99615577	6q16.2	6q16.2		616741	PRDM13	PR domain-containing protein 13	PRDM13	59336	ENSG00000112238			Prdm13 (MGI:2448528)			
chr6	99919909	99994237	6q16.2-q21	6q16.2		606111	"MCHR2, MCH2R, SLT, MCH2"	Melanin-concentrating hormone receptor 2	MCHR2	84539	ENSG00000152034						
chr6	100000000	125800000	6q16.3-q22.31			613828	GEFSP8	"Generalized epilepsy with febrile seizures plus, type 8"		100653381		between D6S962 and D6S287	"Epilepsy, generalized, with febrile seizures plus, type 8, 613828 (2)"				
chr6	100385008	100464928	6q16.3-q21	6q16.3		603128	SIM1	"Single-minded, Drosophila, homolog of, 1"	SIM1	6492	ENSG00000112246		"Obesity, severe, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Sim1 (MGI:98306)			
chr6	100508193	100884454	6q16.3	6q16.3		614217	"ASCC3, p200"	"Activating signal cointegrator 1 complex, subunit 3"	ASCC3	10973	ENSG00000112249			Ascc3 (MGI:1925237)			
chr6	101393707	102070082	6q21	6q16.3		138244	"GRIK2, GLUR6, MRT6"	"Glutamate receptor, ionotropic, kainate 2"	GRIK2	2898	ENSG00000164418		"Mental retardation, autosomal recessive, 6, 611092 (3), Autosomal recessive"	Grik2 (MGI:95815)			
chr6	104682669	104859918	6q21	6q16.3		610876	"HACE1, KIAA1320, SPPRS"	HECT domain- and ankyrin repeat-containing E3 ubiquitin protein ligase 1	HACE1	57531	ENSG00000085382		"Spastic paraplegia and psychomotor retardation with or without seizures, 616756 (3), Autosomal recessive"	Hace1 (MGI:2446110)			
chr6	104936998	105083331	6q21	6q16-q21		611044	LIN28B	"Lin28, C. elegans, homolog of, B"	LIN28B	389421	ENSG00000187772			Lin28b (MGI:3584032)			
chr6	105000000	114200000	6q21			109780	BKMA1	Banded krait minor satellite DNA-1		7951		related to heterogametic sex					
chr6	105000000	114200000	6q21			606325	HTX3	"Heterotaxy, visceral, 3, autosomal"		116629			"?Heterotaxy, visceral, 3, autosomal, 606325 (2)"				
chr6	105000000	114200000	6q21			601666	IDDM15	Insulin-dependent diabetes mellitus-15	IDDM15	3414			"{Diabetes mellitus, insulin-dependent, 15}, 601666 (2)"				
chr6	105000000	114200000	6q21			606460	LGV2	Longevity 2		100329168		associated with rs2802292	"[Longevity 2], 606460 (2)"				
chr6	105000000	114200000	6q21			601349	"MCOPS8, MMEP"	"Microphthalmia, syndromic 8"				translocation with 13q12	"Microphthalmia, syndromic 8, 601349 (2), ?Autosomal dominant"				
chr6	105000000	114200000	6q21			612882	MENAQ2	"Menarche, age at, QTL2"		100302562		associated with rs7759938	"{Menarche, age at, QTL2}, 612882 (2)"				
chr6	105000000	130000000	6q21-q22			608852	PLF	Pulmonary function		450095		close to D6S281	"{Pulmonary function}, 608852 (2)"				
chr6	105096821	105137173	6q21	6q21		604577	"BVES, HBVES, POPDC1, LGMD2X"	Blood vessel epicardial substance	BVES	11149	ENSG00000112276	mutation identified in 1 LGMD2X family	"?Muscular dystrophy, limb-girdle, type 2X, 616812 (3), Autosomal recessive"	Bves (MGI:1346013)			
chr6	105157899	105179982	6q21	6q21		605824	"POPDC3, POP3"	Popeye domain-containing protein 3	POPDC3	64208	ENSG00000132429			Popdc3 (MGI:1930153)			
chr6	105277566	105403123	6q22	6q21		600400	PREP	Prolyl endopeptidase	PREP	5550	ENSG00000085377			Prep (MGI:1270863)			
chr6	106046728	106109938	6q21-q22.1	6q21		603423	"PRDM1, BLIMP1"	PR domain-containing protein 1 (B-lymphocyte-induced maturation protein 1)	PRDM1	639	ENSG00000057657			Prdm1 (MGI:99655)			
chr6	106184475	106325819	6q21	6q21		604261	"ATG5, APG5, APG5L, ASP, SCAR25"	"Autophagy 5, S. cerevisiae, homolog of"	ATG5	9474	ENSG00000057663	mutation identified in one SCAR25 family	"?Spinocerebellar ataxia, autosomal recessive 25, 617584 (3), Autosomal recessive"	Atg5 (MGI:1277186)			
chr6	106360807	106570448	6q21	6q21		601797	"AIM1, ST4"	Absent in melanoma 1	CRYBG1	202	ENSG00000112297			Crybg1 (MGI:109544)			
chr6	106559236	106630920	6q21	6q21		610502	"RTN4IP1, NIMP, OPA10"	Reticulon 4-interacting protein 1	RTN4IP1	84816	ENSG00000130347		"Optic atrophy 10 with or without ataxia, mental retardation, and seizures, 616732 (3), Autosomal recessive"	Rtn4ip1 (MGI:2178759)			
chr6	106629565	106668416	6q21	6q21		617209	"QRSL1, GATA"	Glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like protein 1	QRSL1	55278	ENSG00000130348			Qrsl1 (MGI:1923813)			
chr6	106969830	106976854	6q21	6q21		600074	CD24	CD24 antigen	CD24	100133941	ENSG00000272398	pseudogenes at 15q21-q22; Yq11					
chr6	107065180	107115185	6q21	6q21		616374	"BEND3, KIAA1553"	BEN domain-containing protein 3	BEND3	57673	ENSG00000178409			Bend3 (MGI:2677212)			
chr6	107152556	107459680	6q21	6q21		610564	"PDSS2, DLP1, C6orf210, COQ10D3"	"Prenyl diphosphate synthase, subunit 2"	PDSS2	57107	ENSG00000164494		"Coenzyme Q10 deficiency, primary, 3, 614652 (3), Autosomal recessive"	Pdss2 (MGI:1918615)			
chr6	107490103	107661308	6q21	6q21		613667	"SOBP, JXC1, MRAMS"	"Sine oculis-binding protein, Drosophila, homolog of"	SOBP	55084	ENSG00000112320		"Mental retardation, anterior maxillary protrusion, and strabismus, 613671 (3), Autosomal recessive"	Sobp (MGI:1924427)			
chr6	107867755	107958277	6q21	6q21		608648	"SEC63, PCLD2"	"Sec63, S. cerevisiae, homolog of"	SEC63	11231	ENSG00000025796		"Polycystic liver disease 2, 617004 (3), Autosomal dominant"	Sec63 (MGI:2155302)			
chr6	108041408	108074736	6q21	6q21		607649	"OSTM1, GL, OPTB5"	"Osteopetrosis associated transmembrane protein 1 (grey-lethal, mouse, homolog of)"	OSTM1	28962	ENSG00000081087		"Osteopetrosis, autosomal recessive 5, 259720 (3), Autosomal recessive"	Ostm1 (MGI:2655574)			
chr6	108166057	108188808	6q21	6q21		603849	"NR2E1, TLX"	"Nuclear receptor subfamily 2, group E, member 1 (tailless, Drosophila, homolog of)"	NR2E1	7101	ENSG00000112333			Nr2e1 (MGI:1100526)			
chr6	108211216	108261259	6q21	6q21		605930	SNX3	Sorting nexin 3	SNX3	8724	ENSG00000112335	t(6;13)(q21;q12)		Snx3 (MGI:1860188)			
chr6	108294873	108525783	6q21	6q21		617469	"AFG1L, AFG1, LACE1"	AFG1-like ATPase	AFG1L	246269	ENSG00000135537			Afg1l (MGI:2148801)			
chr6	108559822	108684768	6q21	6q21		602681	"FOXO3A, FOXO3, FKHRL1"	Forkhead box O3A	FOXO3	2309	ENSG00000118689			Foxo3 (MGI:1890081)			
chr6	108986436	109094504	6q21	6q21		606103	"SESN1, SEST1, PA26"	Sestrin 1	SESN1	27244	ENSG00000080546			Sesn1 (MGI:2155278)			
chr6	109366513	109382811	6q21	6q21		603356	"CD164, DFNA66"	CD164 antigen	CD164	8763	ENSG00000135535	mutation identified in 1 DFNA66 family	"?Deafness, autosomal dominant 66, 616969 (3), Autosomal dominant"	Cd164 (MGI:1859568)			
chr6	109444061	109465967	6q16.1	6q21		607129	"MICAL1, NICAL, MICAL"	"Microtubule-associated monooxygenase, calponin and LIM domains-containing 1"	MICAL1	64780	ENSG00000135596			Mical1 (MGI:2385847)			
chr6	109462515	109483236	6q21	6q21		614064	"ZBTB24, PATZ2, ZNF450, KIAA0441, ICF2"	Zinc finger- and BTB domain-containing protein 24	ZBTB24	9841	ENSG00000112365		"Immunodeficiency-centromeric instability-facial anomalies syndrome-2, 614069 (3), Autosomal recessive"	Zbtb24 (MGI:3039618)			
chr6	109492854	109691211	6q21	6q21		615358	AK9	Adenylate kinase 9	AK9	221264	ENSG00000155085			Ak9 (MGI:2685080)			
chr6	109691220	109825430	6q21	6q21		609390	"FIG4, KIAA0274, SAC3, ALS11, YVS, BTOP"	"Fig4, S. cerevisiae, homolog of"	FIG4	9896	ENSG00000112367	mutation identified in 1 BTOP family	"Amyotrophic lateral sclerosis 11, 612577 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 4J, 611228 (3), Autosomal recessive; ?Polymicrogyria, bilateral temporooccipital, 612691 (3), Autosomal recessive; Yunis-Varon syndrome, 216340 (3), Autosomal recessive"	Fig4 (MGI:2143585)			
chr6	109978255	109980719	6q21-q22.1	6q21		600553	GPR6	G protein-coupled receptor-6	GPR6	2830	ENSG00000146360			Gpr6 (MGI:2155249)			
chr6	110099818	110180003	6q21-q22	6q21		605035	"WASF1, WAVE, WAVE1, SCAR1"	WAS protein family member 1	WASF1	8936	ENSG00000112290			Wasf1 (MGI:1890563)			
chr6	110180420	110232219	6q22.1	6q21		605585	"CDC40, PRP17"	"Cell division cycle 40, S. cerevisiae, homolog of"	CDC40	51362	ENSG00000168438			Cdc40 (MGI:1918963)			
chr6	110392179	110415549	6q21	6q21		124450	"DDO, DASOX"	D-aspartate oxidase	DDO	8528	ENSG00000203797			Ddo (MGI:1925528)			
chr6	110424586	110476673	6q21	6q21		608276	"SLC22A16, FLIPT2, CT2"	"Solute carrier family 22 (organic cation transporter), member 16"	SLC22A16	85413	ENSG00000004809			Slc22a16 (MGI:1918090)			
chr6	110609977	110816530	6q21	6q21		614720	"CDK19, KIAA1028"	Cyclin-dependent kinase 19	CDK19	23097	ENSG00000155111			Cdk19 (MGI:1925584)			
chr6	110814620	110895712	6q21-q22	6q21		180980	AMD1	S-adenosylmethionine decarboxylase-1	AMD1	262	ENSG00000123505	pseudogene AMD2 on Xq28		"Amd2,Amd1 (MGI:88004,MGI:1333111)"			
chr6	110958559	110967887	6q21	6q21		611784	"GTF3C6, C6orf51"	"General transcription factor 3C, polypeptide 6"	GTF3C6	112495	ENSG00000155115			Gtf3c6 (MGI:1914621)			
chr6	111087502	111227124	6q21-q22	6q21		607550	"SLC16A10, TAT1"	"Solute carrier family 16 (monocarboxylic acid transporter), member 10"	SLC16A10	117247	ENSG00000112394			Slc16a10 (MGI:1919722)			
chr6	111259278	111280004	6q21	6q21		617331	"MFSD4B, NAGLT1, Kiaa1919"	Major facilitator superfamily domain-containing protein 4B	MFSD4B	91749	ENSG00000173214			Mfsd4b1 (MGI:2143575)			
chr6	111299030	111483714	6q21	6q21		602776	"REV3L, POLZ, REV3"	"Rev-3, yeast, homolog-like (polymerase, DNA, zeta)"	REV3L	5980	ENSG00000009413			Rev3l (MGI:1337131)			
chr6	111555377	111606299	6q21	6q21		607043	"TRAF3IP2, C6orf5, ACT1, CIKS, C6orf4, C6orf6, PSORS13, CANDF8"	TRAF3-interacting protein 2	TRAF3IP2	10758	ENSG00000056972	mutation identified in 1 family with CANDF8	"?Candidiasis, familial, 8, 615527 (3), Autosomal recessive; {Psoriasis susceptibility 13}, 614070 (3)"	Traf3ip2 (MGI:2143599)			
chr6	111660331	111873451	6q21	6q21		137025	FYN	"FYN oncogene related to SRC, FGR, YES"	FYN	2534	ENSG00000010810	proximal 6q21		Fyn (MGI:95602)			
chr6	112052812	112069685	6q22-q23	6q21		603400	"WISP3, PPAC, PPD"	Wnt-1 inducible signaling pathway protein 3	WISP3	8838	ENSG00000112761		"Arthropathy, progressive pseudorheumatoid, of childhood, 208230 (3), Autosomal recessive; Spondyloepiphyseal dysplasia tarda with progressive arthropathy, 208230 (3), Autosomal recessive"	Wisp3 (MGI:2685581)			
chr6	112070656	112087547	6q21	6q21		607345	"TUBE1, TUBE"	"Tubulin, epsilon-1"	TUBE1	51175	ENSG00000074935			Tube1 (MGI:1919174)			
chr6	112107930	112254721	6q21	6q21		600133	"LAMA4, LAMA3, CMD1JJ"	"Laminin, alpha-4"	LAMA4	3910	ENSG00000112769		"Cardiomyopathy, dilated, 1JJ, 615235 (3), Autosomal dominant"	Lama4 (MGI:109321)			
chr6	113857334	113863474	6q22.2	6q21		177061	"MRACKS, MACS, PKCSL"	"Myristoylated alanine-rich protein kinase C substrate (MARCKS, 80K-L)"	MARCKS	4082	ENSG00000277443	monomorphic					
chr6	113936155	113971194	6q21	6q21		605164	HDAC2	Histone deacetylase 2	HDAC2	3066	ENSG00000196591			Hdac2 (MGI:1097691)			
chr6	114055585	114342394	6q22.31	6q21-q22		609407	"HS3ST5, 3OST5"	Heparan sulfate 3-O-sulfotransferase 5	HS3ST5	222537	ENSG00000249853			Hs3st5 (MGI:2441996)			
chr6	114200000	148500000	6q22-q24			609255	5-Feb	"Febrile seizures, familial, 5"	5-Feb	619398		between D6S1572 and D6S472	"Febrile seizures, familial, 5, 609255 (2), Autosomal dominant"				
chr6	114200000	148500000	6q22-q24			606035	FIQTL1	Fasting insulin level quantitative trait locus 1		619503		max lod at D6S1569	"[Fasting insulin level quantitative trait locus 1], 606035 (2)"				
chr6	114200000	138300000	6q22-q23			161950	IGAN1	"IgA nephropathy, susceptibility to, 1"		60498			"{IgA nephropathy, susceptibility to, 1}, 161950 (2), ?Autosomal dominant"				
chr6	114200000	138300000	6q22-q23			604201	SM2	Hepatic fibrosis susceptibility due to Schistosoma mansoni infection		53366		?polymorphism of INFGR1	"{Hepatic fibrosis susceptibility due to Schistosoma mansoni infection}, 604201 (2)"				
chr6	115941030	116100738	6q21-q22.3	6q22.1		606573	"FRK, RAK, GTK"	FYN-related kinase	FRK	2444	ENSG00000111816			Frk (MGI:103265)			
chr6	116118908	116219936	6q21-q22.3	6q22.1		120110	COL10A1	"Collagen X, alpha-1 polypeptide"	COL10A1	1300	ENSG00000123500		"Metaphyseal chondrodysplasia, Schmid type, 156500 (3), Autosomal dominant"	Col10a1 (MGI:88445)			
chr6	116254151	116441260	6q22	6q22.1		605942	"DSE, SART2, EDSMC2"	Dermatan sulfate epimerase	DSE	29940	ENSG00000111817		"Ehlers-Danlos syndrome, musculocontractural type 2, 615539 (3), Autosomal recessive"	Dse (MGI:2443455)			
chr6	116274858	116280116	6q22-q23	6q22.1		604714	"TSPYL1, TSPYL, SIDDT"	Y-encoded testis-specific protein-like	TSPYL1	7259	ENSG00000189241		"Sudden infant death with dysgenesis of the testes syndrome, 608800 (3), Autosomal recessive"	Tspyl1 (MGI:1298395)			
chr6	116461369	116463781	6q22.1	6q22.1		617305	"FAM26F, INAM"	"Family with sequence similarity 26, member F"	CALHM6	441168	ENSG00000188820			Fam26f (MGI:2443082)			
chr6	116496482	116545609	6q22.1	6q22.1		614137	"BET3L, TRAPPC3L"	"Bet3, S. cerevisiae, homolog-like"	TRAPPC3L	100128327	ENSG00000173626			Trappc3l (MGI:3642034)			
chr6	116598183	116633050	6q22.1	6q22.1		612647	"RSPH4A, CILD11"	"Radial spoke head 4, Chlamydomonas, homolog of, A"	RSPH4A	345895	ENSG00000111834		"Ciliary dyskinesia, primary, 11, 612649 (3)"	Rsph4a (MGI:3027894)			
chr6	116677642	116741866	6q22.1	6q22.1		604545	KPNA5	Karyopherin alpha-5	KPNA5	3841	ENSG00000196911						
chr6	116877212	116932162	6q22.2	6q22.1		612659	"RFX6, RFXDC1, MTCHRS"	"Regulatory factor X, 6"	RFX6	222546	ENSG00000185002		"Mitchell-Riley syndrome, 615710 (3), Autosomal recessive"	Rfx6 (MGI:2445208)			
chr6	117265557	117273564	6q21	6q22.1		609979	"VGLL2, VGL2, VITO1"	Vestigial-like 2	VGLL2	245806	ENSG00000170162			Vgll2 (MGI:2447460)			
chr6	117287917	117426064	6q22	6q22.1		165020	"ROS1, MCF3"	Avian UR2 sarcoma virus oncogene (v-ros) homolog 1	ROS1	6098	ENSG00000047936			Ros1 (MGI:97999)			
chr6	117560268	117602541	6q21	6q22.1		606845	"GOPC, PIST, FIG, CAL"	Golgi-associated PDZ and coiled-coil domains-containing protein	GOPC	57120	ENSG00000047932			Gopc (MGI:2149946)			
chr6	117675459	117710726	6q22.31	6q22.1		610463	"NUS1, NGBR, C6orf68, CDG1AA, MRD55"	"Nuclear undecaprenyl pyrophosphate synthase 1, S. cerevisiae, homolog of"	NUS1	116150	ENSG00000153989	mutation identified in 1 CDG1AA family	"?Congenital disorder of glycosylation, type 1aa, 617082 (3), Autosomal recessive; Mental retardation, autosomal dominant 55, with seizures, 617831 (3), Autosomal dominant"	Nus1 (MGI:1196365)			
chr6	118100000	130900000	6q22.3-q23.1			142470	"HBFQTL2, FCP"	Fetal hemoglobin quantitative trait locus 2		7954			"Fetal hemoglobin quantitative trait locus 2, 142470 (2), Autosomal dominant"				
chr6	118548262	118561714	6q22.1	6q22.31		172405	"PLN, PLB, CMD1P, CMH18"	Phospholamban	PLN	5350	ENSG00000198523		"Cardiomyopathy, dilated, 1P, 609909 (3); Cardiomyopathy, hypertrophic, 18, 613874 (3), Autosomal dominant"				
chr6	118813448	118935161	6q22.1-q22.33	6q22.31		610098	"MCM9, MCMDC1, ODG4"	Minichromosome maintenance complex component 9	MCM9	254394	ENSG00000111877		"Ovarian dysgenesis 4, 616185 (3), Autosomal recessive"	Mcm9 (MGI:1918817)			
chr6	118894076	118909170	6q22.31	6q22.31		609189	"ASF1A, CIA"	"Anti-silencing function 1, S. cerevisiae, homolog of, A"	ASF1A	25842	ENSG00000111875			Asf1a (MGI:1913653)			
chr6	119177200	119350618	6q22	6q22.31		604344	MAN1A1	"Mannosidase, alpha, class 1A, member 1"	MAN1A1	4121	ENSG00000111885			Man1a (MGI:104677)			
chr6	121079493	121335383	6q22.31	6q22.31		615867	"TBC1D32, BROMI"	"TBC1 domain family, member 32"	TBC1D32	221322	ENSG00000146350			Tbc1d32 (MGI:2442827)			
chr6	121435576	121449743	5q22.31	6q22.31		121014	"GJA1, CX43, ODDD, SDTY3, ODOD, HSS, AVSD3, HLHS1, CMDR, EKVP3"	"Gap junction protein, alpha-1, 43kD (connexin 43)"	GJA1	2697	ENSG00000152661	pseudogene on chr.5	"Atrioventricular septal defect 3, 600309 (3), Autosomal dominant; Craniometaphyseal dysplasia, autosomal recessive, 218400 (3), Autosomal recessive; Erythrokeratodermia variabilis et progressiva 3, 617525 (3), Autosomal dominant; Hypoplastic left heart syndrome 1, 241550 (3), Autosomal recessive; Oculodentodigital dysplasia, 164200 (3), Autosomal dominant; Oculodentodigital dysplasia, autosomal recessive, 257850 (3), Autosomal recessive; Palmoplantar keratoderma with congenital alopecia, 104100 (3), Autosomal dominant; Syndactyly, type III, 186100 (3), Autosomal dominant"	Gja1 (MGI:95713)			
chr6	122399550	122433118	6q22.3	6q22.31		140581	HSF2	Heat-shock transcription factor 2	HSF2	3298	ENSG00000025156			Hsf2 (MGI:96239)			
chr6	122443347	122471880	6q22.31	6q22.31		614548	"SERINC1, TMS2, KIAA1253"	Serine incorporator 1	SERINC1	57515	ENSG00000111897			Serinc1 (MGI:1926228)			
chr6	122471916	122726372	6q22.31	6q22.31		606914	PKIB	"Protein kinase, cAMP-dependent catalytic, inhibitor beta"	PKIB	5570	ENSG00000135549			Pkib (MGI:101937)			
chr6	122749200	122784076	6q22-q23	6q22.31		602965	"FABP7, FABPB, BLBP"	Fatty acid-binding protein 7	FABP7	2173	ENSG00000164434			Fabp7 (MGI:101916)			
chr6	122788455	122809719	6q22.31	6q22.31		610728	"SMPDL3A, ASML3A"	"Sphingomyelin phosphodiesterase, acid-like, 3A"	SMPDL3A	10924	ENSG00000172594			Smpdl3a (MGI:1931437)			
chr6	122995970	123072919	6q22.31	6q22.31		616945	CLVS2	Clavesin 2	CLVS2	134829	ENSG00000146352			Clvs2 (MGI:2443223)			
chr6	123216338	123637092	6q22-q23	6q22.31		603283	"TRDN, TDN, CPVT5"	Triadin	TRDN	10345	ENSG00000186439		"Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 (3), Autosomal recessive"	Trdn (MGI:1924007)			
chr6	123803841	124825651	6q21	6q22.31		609758	"NKAIN2, TCBA"	Na+/K+ transporting ATPase interacting 2	NKAIN2	154215	ENSG00000188580	fused with SUSP1 in T-cell lymphoma/leukemia		Nkain2 (MGI:1923447)			
chr6	124908242	124963026	6q23	6q22.31		602532	STL	Six-twelve leukemia gene	RNF217-AS1	7955							
chr6	125153728	125264406	6q22.31	6q22.31		604069	"TPD52L1, D53"	Tumor protein D52-like 1	TPD52L1	7164	ENSG00000111907			Tpd52l1 (MGI:1298386)			
chr6	125747638	125762242	6q21	6q22.31		604674	"HEY2, HERP1, GRL"	Hairy/enhancer of split-related with YRPW motif 2	HEY2	23493	ENSG00000135547			Hey2 (MGI:1341884)			
chr6	125780942	125932029	6q22.33	6q22.31-q22.32		609752	"NCOA7, ERAP140"	Nuclear receptor coactivator 7	NCOA7	135112	ENSG00000111912			Ncoa7 (MGI:2444847)			
chr6	125956714	125980243	6q22.33	6q22.32		609998	HINT3	Histidine triad nucleotide-binding protein 3	HINT3	135114	ENSG00000111911			Hint3 (MGI:1914097)			
chr6	126339695	126483319	6q22.32	6q22.32		611264	"CEMPW, C6orf173, CUG2"	Centromeric protein W	CENPW	387103	ENSG00000203760			Cenpw (MGI:1913561)			
chr6	127118670	127199480	6q22.2	6q22.33		610574	"RSPO3, PWTSR, CRISTIN1"	R-spondin family member 3	RSPO3	84870	ENSG00000146374			Rspo3 (MGI:1920030)			
chr6	127263414	127289892	6q22.1-q22.33	6q22.33		612137	RNF146	Ring finger protein 146	RNF146	81847	ENSG00000118518			Rnf146 (MGI:1915281)			
chr6	127288711	127344178	6q22.33	6q22.33		612136	ECHDC1	Enoyl coenzyme A hydratase domain-containing protein 1	ECHDC1	55862	ENSG00000093144			Echdc1 (MGI:1277169)			
chr6	127708193	127918630	6q22.33	6q22.33		613607	"THEMIS, GASP, SPOT, C6orf190"	Thymocyte-expressed molecule involved in selection	THEMIS	387357	ENSG00000172673			Themis (MGI:2443552)			
chr6	127968778	128520673	6q22.2-q22.3	6q22.33		602545	PTPRK	"Protein-tyrosine phosphatase, receptor type, kappa"	PTPRK	5796	ENSG00000152894			Ptprk (MGI:103310)			
chr6	128883140	129516565	6q22-q23	6q22.33		156225	"LAMA2, LAMM"	"Laminin, alpha-2 (merosin)"	LAMA2	3908	ENSG00000196569		"Muscular dystrophy, congenital merosin-deficient, 607855 (3), Autosomal recessive; Muscular dystrophy, congenital, due to partial LAMA2 deficiency, 607855 (3), Autosomal recessive"	Lama2 (MGI:99912)			
chr6	129576144	129710224	6q22-q24	6q22.33		613351	ARHGAP18	RHO GTPase-activating protein 18	ARHGAP18	93663	ENSG00000146376			Arhgap18 (MGI:1921160)			
chr6	130000000	160600000	6q23-q25			607446	BMIQ3	Body mass index quantitative trait locus 3	BMIQ3	337895		max lod at D6S305	"[Body mass index QTL3], 607446 (2)"				
chr6	130000000	138300000	6q23			602067	"CMD1F, CDCD3, LGMD1D"	"Cardiomyopathy, dilated-1F, autosomal dominant"					"Cardiomyopathy, dilated, 1F and limb-girdle muscular dystrophy type 1D, 602067 (2)"				
chr6	130000000	138300000	6q23			609319	HCHGQ1	Hematocrit/hemoglobin quantitative trait locus 1		100381204			"[Hematocrit/hemoglobin quantitative trait locus 1], 609319 (2)"				
chr6	130000000	160600000	6q23-q25			608935	LNCR1	Lung cancer 1		450093		max hlod at D6S2436	"{Lung cancer susceptibility}, 608935 (2)"				
chr6	130000000	148500000	6q23-q24			611536	"MAFD6, BPAD"	Major affective disorder 6		100188844			"{Major affective disorder 6}, 611536 (2)"				
chr6	130000000	148500000	6q23-q24			602154	NTT	Noncoding transcript in T cells		7956							
chr6	130000000	138300000	6q23			180300	RA	"Rheumatoid arthritis, susceptibility to"				associated with SNP rs10499194 and rs6920220	"{Rheumatoid arthritis, susceptibility to}, 180300 (2)"				
chr6	130000000	138300000	6q23			614494	RP63	Retinitis pigmentosa 63	RP63	100862681		between D6S457 and D6S1656	"Retinitis pigmentosa 63, 614494 (2), Autosomal dominant"				
chr6	130000000	138300000	6q23			612378	SLEB13	"Systemic lupus erythematosus, susceptibility to, 13"		100196918		associated with rs5029939	"{Systemic lupus erythematosus, susceptibility to, 13}, 612378 (2)"				
chr6	130000000	142200000	6q23-q24.1			608220	SPG25	"Spastic paraplegia 25, autosomal recessive, with disc herniation"	SPG25	387583			"Spastic paraplegia 25, autosomal recessive, 608220 (2), Autosomal recessive"				
chr6	130827954	131063321	6q22-q23	6q23.1-q23.2		603237	EPB41L2	Erythrocyte membrane protein band 4.1-like 2	EPB41L2	2037	ENSG00000079819			Epb41l2 (MGI:103009)			
chr6	131573158	131584331	6q23	6q23.2		608313	ARG1	"Arginase, liver"	ARG1	383	ENSG00000118520		"Argininemia, 207800 (3), Autosomal recessive"	Arg1 (MGI:88070)			
chr6	131573965	131628238	6q23.2	6q23.2		605042	"MED23, MRT18"	Mediator complex subunit 23	MED23	9439	ENSG00000112282		"Mental retardation, autosomal recessive 18, 614249 (3), Autosomal recessive"	Med23 (MGI:1917458)			
chr6	131637234	131747412	6q22	6q23.2		602182	"ENPP3, PDNP3"	Ectonucleotide pyrophosphatase/phosphodiesterase 3	ENPP3	5169	ENSG00000154269			Enpp3 (MGI:2143702)			
chr6	131808015	131895154	6q22-q23	6q23.2		173335	"ENPP1, PDNP1, NPPS, M6S1, PCA1, ARHR2, COLED"	"Ectonucleotide pyrophosphatase/phosphodiesterase 1 (Ly-41 antigen, mouse, homolog of)"	ENPP1	5167	ENSG00000197594		"Arterial calcification, generalized, of infancy, 1, 208000 (3), Autosomal recessive; Cole disease, 615522 (3), Autosomal dominant; {Diabetes mellitus, non-insulin-dependent, susceptibility to}, 125853 (3), Autosomal dominant; Hypophosphatemic rickets, autosomal recessive, 2, 613312 (3); {Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Enpp1 (MGI:97370)			
chr6	131948175	131951377	6q23.1	6q23.2		121009	"CTGF, NOV2"	Connective tissue growth factor	CTGF	1490	ENSG00000118523	proximal to MYB		Ctgf (MGI:95537)			
chr6	132296054	132401533	6q23.1-q23.3	6q23.2		609000	"MOXD1, MOX"	"Monooxygenase, DBH-like, 1"	MOXD1	26002	ENSG00000079931			Moxd1 (MGI:1921582)			
chr6	132457523	132513471	6q23.2	6q23.2		603217	STX7	Syntaxin 7	STX7	8417	ENSG00000079950			Stx7 (MGI:1858210)			
chr6	132538287	132539335	6q23.2	6q23.2		608282	"TAR3, TA3"	Trace amine receptor 3	TAAR9	134860	ENSG00000237110			Taar9 (MGI:3527454)			
chr6	132552683	132553730	6q23.2	6q23.2		606927	"GPR102, TA5"	G protein-coupled receptor 102	TAAR8	83551	ENSG00000146385			"Taar8c,Taar8b,Taar8a (MGI:2685995,MGI:3527452,MGI:2685076)"			
chr6	132570321	132571358	6q23.2	6q23.2		608923	"TAAR6, TRAR4"	Trace amine-associated receptor 6	TAAR6	319100	ENSG00000146383			Taar6 (MGI:2685074)			
chr6	132588591	132589737	6q23.2	6q23.2		607405	PNR	Putative neurotransmitter receptor	TAAR5	9038	ENSG00000135569			Taar5 (MGI:2685073)			
chr6	132617149	132624274	6q24	6q23.2		604849	"TAAR2, GPR58"	Trace amine-associated receptor 2	TAAR2	9287	ENSG00000146378			Taar2 (MGI:2685071)			
chr6	132644897	132646025	6q23.1	6q23.2		609333	"TAAR1, TA1"	Trace amine-associated receptor 1	TAAR1	134864	ENSG00000146399			Taar1 (MGI:2148258)			
chr6	132680857	132714054	6q23-q24	6q23.2		603570	"VNN1, HDLCQ8"	Vanin 1	VNN1	8876	ENSG00000112299		[High density lipoprotein cholesterol level QTL 8] (3)	Vnn1 (MGI:108395)			
chr6	132722786	132734764	6q23-q24	6q23.2		606592	VNN3	Vanin 3	VNN3	55350	ENSG00000093134						
chr6	132743502	132763488	6q23-q24	6q23.2		603571	VNN2	Vanin 2	VNN2	8875	ENSG00000112303						
chr6	132769367	132798655	6q22.3	6q23.2		613361	C6orf192	Chromosome 6 open reading frame 192	SLC18B1	116843	ENSG00000146409			Slc18b1 (MGI:1923556)			
chr6	132814568	132817563	6q	6q23.2		603660	RPS12	Ribosomal protein S12	RPS12	6206	ENSG00000112306			Rps12 (MGI:98105)			
chr6	133240339	133532119	6q23	6q23.2		603550	"EYA4, DFNA10, CMD1J"	"Eyes absent, Drosophila, homolog of, 4"	EYA4	2070	ENSG00000112319		"Cardiomyopathy, dilated, 1J, 605362 (3); Deafness, autosomal dominant 10, 601316 (3), Autosomal dominant"	Eya4 (MGI:1337104)			
chr6	133502251	133889005	6q23.2	6q23.2		616058	TARID	TCF21 antisense RNA inducing promoter demethylation	TARID	100507308							
chr6	133889120	133895536	6q23-q24	6q23.2		603306	"TCF21, POD1"	Transcription factor-21 (epicardin; podocyte-expressed 1)	TCF21	6943	ENSG00000118526			Tcf21 (MGI:1202715)			
chr6	133987580	134052650	6q23.2	6q23.2		610372	"SLC2A12, GLUT12"	"Solute carrier family 2 (facilitated glucose transporter), member 12"	SLC2A12	154091	ENSG00000146411			Slc2a12 (MGI:3052471)			
chr6	134169245	134318111	6q23	6q23.2		602958	SGK1	Serum/glucocorticoid-regulated kinase 1	SGK1	6446	ENSG00000118515			Sgk1 (MGI:1340062)			
chr6	134700000	138300000	6q23.3			614645	MPVQTL5	Mean platelet volume quantitative trait locus 5		100887752		associated with rs9399137	"Mean platelet volume QTL5, 614645 (2)"				
chr6	134917389	134950121	6q23.2	6q23.3		606467	"ALDH8A1, ALDH12"	"Aldehyde dehydrogenase 8 family, member A1"	ALDH8A1	64577	ENSG00000118514			Aldh8a1 (MGI:2653900)			
chr6	134960377	135054897	6q24	6q23.3		612450	"HBS1L, KIAA1038, ERFS"	HBS1-like protein	HBS1L	10767	ENSG00000112339			Hbs1l (MGI:1891704)			
chr6	135181314	135219172	6q22	6q23.3		189990	MYB	Avian myeloblastosis viral (v-myb) oncogene homolog	MYB	4602	ENSG00000118513		{T-cell acute lymphoblastic leukemia} (3)	Myb (MGI:97249)			
chr6	135283971	135497770	6q23.3	6q23.3		608894	AHI1	Abelson helper integration site 1	AHI1	54806	ENSG00000135541		"Joubert syndrome 3, 608629 (3), Autosomal recessive"	Ahi1 (MGI:87971)			
chr6	135851695	136195570	6q23.3	6q23.3		604645	PDE7B	"Phosphodiesterase 7B, cAMP-specific, high-affinity"	PDE7B	27115	ENSG00000171408			Pde7b (MGI:1352752)			
chr6	136256862	136289850	6q22-q23	6q23.3		612588	"BCLAF1, BTF, KIAA0164"	BCL2-associated transcription factor 1	BCLAF1	9774	ENSG00000029363			Bclaf1 (MGI:1917580)			
chr6	136342280	136550818	6q22-q25	6q23.3		604108	"MAP7, EMAP115"	Microtubule-associated protein-7	MAP7	9053	ENSG00000135525			Map7 (MGI:1328328)			
chr6	136557045	136793097	6q22.33	6q23.3		602448	"MAP3K5, MEKK5, MAPKKK5, ASK1"	Mitogen-activated protein kinase kinase kinase 5	MAP3K5	4217	ENSG00000197442			Map3k5 (MGI:1346876)			
chr6	136821682	136913933	6q23.3	6q23.3		601757	"PEX7, RCDP1, PBD9B"	Peroxisomal biogenesis factor-7	PEX7	5191	ENSG00000112357		"Peroxisome biogenesis disorder 9B, 614879 (3); Rhizomelic chondrodysplasia punctata, type 1, 215100 (3), Autosomal recessive"	Pex7 (MGI:1321392)			
chr6	136922240	136925659	6q23.3	6q23.3		612519	SLC35D3	"Solute carrier family 35, member D3"	SLC35D3	340146	ENSG00000182747			Slc35d3 (MGI:1923407)			
chr6	136999970	137045179	6q23	6q23.3		605620	IL20RA	"Interleukin 20 receptor, alpha"	IL20RA	53832	ENSG00000016402			Il20ra (MGI:3605069)			
chr6	137143819	137173647	6q24.1-q24.2	6q23.3		606648	"IL22BP, IL22RA2"	Interleukin 22-binding protein	IL22RA2	116379	ENSG00000164485			Il22ra2 (MGI:2665114)			
chr6	137197483	137220350	6q23.3	6q23.3		107470	"IFNGR1, IMD27A, IMD27B"	"Immune interferon, receptor for"	IFNGR1	3459	ENSG00000027697		"{H. pylori infection, susceptibility to}, 600263 (3); {Hepatitis B virus infection, susceptibility to}, 610424 (3); Immunodeficiency 27A, mycobacteriosis, AR, 209950 (3), Autosomal recessive; Immunodeficiency 27B, mycobacteriosis, AD, 615978 (3), Autosomal dominant; {Tuberculosis infection, protection against}, 607948 (3); {Tuberculosis, susceptibility to}, 607948 (3)"	Ifngr1 (MGI:107655)			
chr6	137492198	137494393	6q23.3	6q23.3		609323	"OLIG3, BHLHB7"	Oligodendrocyte lineage transcription factor 3	OLIG3	167826	ENSG00000177468			Olig3 (MGI:2149955)			
chr6	137866316	137883313	6q23	6q23.3		191163	"TNFAIP3, A20, OTUD7C, AISBL"	Tumor necrosis factor-alpha-induced protein 3	TNFAIP3	7128	ENSG00000118503		"Autoinflammatory syndrome, familial, Behcet-like, 616744 (3), Autosomal dominant"	Tnfaip3 (MGI:1196377)			
chr6	138088504	138107522	6q23.3	6q23.3		609301	PERP	p53 effector related to PMP22	PERP	64065	ENSG00000112378			Perp (MGI:1929938)			
chr6	138161689	138344662	6q23.3-q24.1	6q23.3-q24.1		617411	"ARFGEF3, BIG3, KIAA1244"	ADP-ribosylation factor guanine nucleotide exchange factor 3	ARFGEF3	57221	ENSG00000112379			Arfgef3 (MGI:106387)			
chr6	138215985	138218489	6q23-q24	6q23.3		605669	"PBOV1, UROC28, UC28"	Prostate and breast cancer overexpressed 1	PBOV1	59351	ENSG00000254440						
chr6	138300000	160600000	6q24-q25			612863	"DEL6q24q25, C6DELq25q25"	Chromosome 6q24-q25 deletion syndrome					"Chromosome 6q25-q25 deletion syndrome, 612863 (4)"				
chr6	138300000	160600000	6q24-q25			606255	STQTL1	Stature quantitative trait locus 1				associated with rs4896582 and rs3748069	"{Stature QTL 1}, 606255 (2)"				
chr6	138403530	138413444	6q24	6q24.1		605825	"C6orf34, SOUL"	"Soul, chicken, homolog of"	HEBP2	23593	ENSG00000051620			Hebp2 (MGI:1860084)			
chr6	138773516	138793318	6q24.1	6q24.1		615353	"CCDC28A, C6orf80"	Coiled-coil domain-containing 28A	CCDC28A	25901	ENSG00000024862			Ccdc28a (MGI:2443508)			
chr6	138904014	138988260	6q23.1-q24.1	6q24.1		614825	"REPS1, NBIA7"	RALBP1-associated EPS domain-containing protein 1	REPS1	85021	ENSG00000135597	mutation identified in 1 NBIA7 family	"?Neurodegeneration with brain iron accumulation 7, 617916 (3), Autosomal recessive"	Reps1 (MGI:1196373)			
chr6	139135111	139180808	6q24.1	6q24.1		607977	"HECA, HDC"	"Headcase, Drosophila, homolog of"	HECA	51696	ENSG00000112406			Heca (MGI:2685715)			
chr6	139372254	139374649	6q23.3	6q24.1		602937	"CITED2, MRG1, P35SRJ, VSD2, ASD8"	"CBP/p300-interacting transactivator, with glu/asp-rich C-terminal domain, 2"	CITED2	10370	ENSG00000164442	?pseudogene on 1q22	"Atrial septal defect 8, 614433 (3), Autosomal dominant; Ventricular septal defect 2, 614431 (3), Autosomal dominant"	Cited2 (MGI:1306784)			
chr6	142074483	142147204	6q21-qter	6q24.1		162341	NMBR	Neuromedin B receptor	NMBR	4829	ENSG00000135577			Nmbr (MGI:1100525)			
chr6	142147161	142220947	6q24.1	6q24.1-q24.2		610902	"C6orf55, SBP1, LIP5, VTA1, DRG1"	SKD1-binding protein 1	VTA1	51534	ENSG00000009844			Vta1 (MGI:1913451)			
chr6	142200000	155200000	6q24.2-q25.2			127500	"DUH1, DUH"	Dyschromatosis universalis hereditaria 1		387570		max lod at D6S1553	"Dyschromatosis universalis hereditaria 1, 127500 (2), Autosomal dominant"				
chr6	142301918	142446265	6q24.1	6q24.2		612243	"ADGRG6, PR126, VIGR, LCCS9"	Adhesion G protein-coupled receptor G6	ADGRG6	57211	ENSG00000112414		"Lethal congenital contracture syndrome 9, 616503 (3), Autosomal recessive"	Adgrg6 (MGI:1916151)			
chr6	142751466	142945755	6q23-q24	6q24.2		143054	"HIVEP2, MRD43"	Human immunodeficiency virus type I enhancer-binding protein-2	HIVEP2	3097	ENSG00000010818		"Mental retardation, autosomal dominant 43, 616977 (3), Autosomal dominant"	Hivep2 (MGI:1338076)			
chr6	143422831	143450749	6q24.2	6q24.2		615388	"ADAT2, TAD2"	"Adenosine deaminase, tRNA-specific, 2"	ADAT2	134637	ENSG00000189007			Adat2 (MGI:1914007)			
chr6	143450780	143490615	6q24.2	6q24.2		603164	"PEX3, PBD10A, PBD10B"	Peroxisomal biogenesis factor-3	PEX3	8504	ENSG00000034693	mutation identified in 1 PBD10B patient	"Peroxisome biogenesis disorder 10A (Zellweger), 614882 (3), Autosomal recessive; ?Peroxisome biogenesis disorder 10B, 617370 (3), Autosomal recessive"	Pex3 (MGI:1929646)			
chr6	143494811	143511882	6q24.2	6q24.2		136820	FUCA2	"Fucosidase, alpha-L- 2, plasma"	FUCA2	2519	ENSG00000001036	linked to PLG		Fuca2 (MGI:1914098)			
chr6	143608179	143831184	6q24.2	6q24.2		608724	"PHACTR2, KIAA0680"	Phosphatase and actin regulator 2	PHACTR2	9749	ENSG00000112419			Phactr2 (MGI:2446138)			
chr6	143940299	144064598	6q24	6q24.2		603044	"PLAGL1, ZAC, LOT1"	Pleomorphic adenoma gene-like 1 (ZAC tumor suppressor)	PLAGL1	5325	ENSG00000118495	relaxed imprinting in TNDM	"{Diabetes mellitus, transient neonatal}, 601410 (1)"	Plagl1 (MGI:1100874)			
chr6	144004915	144008729	6q24	6q24.2		606546	HYMAI	Hydatidiform mole-associated and imprinted transcript	HYMAI	57061							
chr6	144094880	144095616	6q24.2	6q24.2		617847	"SF3B5, SF3B10"	"Splicing factor 3B, subunit 5"	SF3B5	83443	ENSG00000169976			Sf3b5 (MGI:1913375)			
chr6	144140043	144191938	6q24	6q24.2		605014	"STX11, FHL4, HPLH4, HLH4"	Syntaxin-11	STX11	8676	ENSG00000135604		"Hemophagocytic lymphohistiocytosis, familial, 4, 603552 (3), Autosomal recessive"	Stx11 (MGI:1921982)			
chr6	144284954	144853033	6q24	6q24.2		128240	"UTRN, DMDL, DRP1"	Utrophin (homologous to dystrophin)	UTRN	7402	ENSG00000152818	near dy in mouse		Utrn (MGI:104631)			
chr6	145382539	145736020	6q24	6q24.3		607566	"EPM2A, MELF, EPM2"	Laforin	EPM2A	7957	ENSG00000112425		"Epilepsy, progressive myoclonic 2A (Lafora), 254780 (3), Autosomal recessive"	Epm2a (MGI:1341085)			
chr6	145798134	145864408	6q24	6q24.3		609101	"FBXO30, FBX30"	F-box only protein 30	FBXO30	84085	ENSG00000118496			Fbxo30 (MGI:1919115)			
chr6	146027633	146437597	6q24	6q24.3		604473	"GRM1, MGLUR1, GRM1A, SCAR13, SCA44"	"Glutamate receptor, metabotropic, 1"	GRM1	2911	ENSG00000152822		"Spinocerebellar ataxia 44, 617691 (3), Autosomal dominant; Spinocerebellar ataxia, autosomal recessive 13, 614831 (3), Autosomal recessive"	Grm1 (MGI:1351338)			
chr6	146543691	146554955	6q24.3	6q24.3		612906	RAB32	Ras-associated protein RAB32	RAB32	10981	ENSG00000118508			Rab32 (MGI:1915094)			
chr6	146598964	146815461	6q24.3	6q24.3		614630	ADGB	Androglobin	ADGB	79747	ENSG00000118492			Adgb (MGI:3605549)			
chr6	147204183	147390475	6q24.3	6q24.3		604586	STXBP5	Syntaxin-binding protein 5 (tomosyn)	STXBP5	134957	ENSG00000164506			Stxbp5 (MGI:1926058)			
chr6	148193439	148552049	6q24.3	6q24.3-q25.1		607955	"SASH1, KIAA0790"	Sterile alpha motifs- and SH3 domain-containing protein 1	SASH1	23328	ENSG00000111961			Sash1 (MGI:1917347)			
chr6	148500000	160600000	6q25			612114	BMND11	Bone mineral density quantitative trait locus 11		100188884		"associated with rs4870044, rs1038304, and rs1999805"	"[Bone mineral density QTL 11], 612114 (2)"				
chr6	148500000	160600000	6q25			612521	IDDM21	"Diabetes mellitus, insulin-dependent, 21"				associated with rs1738074	"{Diabetes mellitus, insulin-dependent, 21}, 612521 (2)"				
chr6	148500000	170805979	6q25-q27			600883	IDDM8	Insulin-dependent diabetes mellitus-8	IDDM8	3407			"{Diabetes mellitus, insulin-dependent, 8}, 600883 (2)"				
chr6	148500000	164100000	6q25-q26			180020	RCD1	Retinal cone dystrophy-1	RCD1	5953			"?Retinal cone dystrophy-1, 180020 (2), Autosomal dominant"				
chr6	148745890	149076989	6q25.1	6q25.1		610752	UST	Uronyl 2-sulfotransferase	UST	10090	ENSG00000111962			Ust (MGI:2442406)			
chr6	149217923	149411612	6q25	6q25.1		605101	"TAB2, MAP3K7IP2, KIAA0733, CHTD2"	Tak1 (MAP3K7) binding protein 2	TAB2	23118	ENSG00000055208		"Congenital heart defects, nonsyndromic, 2, 614980 (3), Autosomal dominant"	Tab2 (MGI:1915902)			
chr6	149400358	149401045	6q25	6q25.1		608829	"SUMO4, IDDM5"	Small ubiquitin-like modifier 4	SUMO4	387082	ENSG00000177688		"{Diabetes mellitus, insulin-dependent, 5}, 600320 (3)"				
chr6	149447629	149485011	6q25.1	6q25.1		611106	"ZC3H12D, p34, C6orf95"	Zinc finger CCCH domain-containing protein 12D	ZC3H12D	340152	ENSG00000178199			Zc3h12d (MGI:3045313)			
chr6	149504494	149546101	6q24-q25	6q25.1		607609	PPIL4	Peptidyl-prolyl isomerase-like 4	PPIL4	85313	ENSG00000131013			Ppil4 (MGI:1914668)			
chr6	149594872	149649017	6q25.1	6q25.1		606696	KATNA1	"Katanin, p60 subunit, A1"	KATNA1	11104	ENSG00000186625			Katna1 (MGI:1344353)			
chr6	149658152	149718255	6q25.1	6q25.1		603473	LATS1	"Large tumor suppressor, Drosophila, homolog of, 1"	LATS1	9113	ENSG00000131023			Lats1 (MGI:1333883)			
chr6	149724314	149746571	6q24.3	6q25.1		608141	NUP43	"Nucleoporin, 43kD"	NUP43	348995	ENSG00000120253			Nup43 (MGI:1917162)			
chr6	149749694	149811420	6q22.3-q24	6q25.1		176851	PCMT1	Protein-L-isoaspartate (D-aspartate) O-methyltransferase	PCMT1	5110	ENSG00000120265						
chr6	149941937	149949234	6q25	6q25.1		605698	ULBP2	UL16-binding protein 2	ULBP2	80328	ENSG00000131015						
chr6	149963973	149973714	6q25	6q25.1		605697	ULBP1	UL16-binding protein 1	ULBP1	80329	ENSG00000111981			Ulbp1 (MGI:1925027)			
chr6	150018333	150025595	6q24.2-q25.3	6q25.1		611047	RAET1L	Retinoic acid early transcript 1L	RAET1L	154064	ENSG00000155918						
chr6	150061045	150069146	6q25	6q25.1		605699	ULBP3	UL16-binding protein 3	ULBP3	79465	ENSG00000131019						
chr6	150143051	150250391	6q24.3-q25.3	6q25.1		613242	"PPP1R14C, KEPI"	"Protein phosphatase 1, regulatory subunit 14C"	PPP1R14C	81706	ENSG00000198729			Ppp1r14c (MGI:1923392)			
chr6	150368853	150404628	6q24-q25	6q25.1		612025	"IYD, DEHAL1, TDH4"	Iodotyrosine deiodinase	IYD	389434	ENSG00000009765		"Thyroid dyshormonogenesis 4, 274800 (3), Autosomal recessive"	Iyd (MGI:1917587)			
chr6	150865678	151101886	6q25.2	6q25.1		611427	"MTHFD1L, MTC1THFS"	"Methylenetetrahydrofolate dehydrogenase 1-like, NADP(+)-dependent"	MTHFD1L	25902	ENSG00000120254			Mthfd1l (MGI:1924836)			
chr6	151364114	151391704	6q25.1	6q25.1		616595	"ZBTB2, ZNF437, KIAA1483"	Zinc finger- and BTB domain-containing protein 2	ZBTB2	57621	ENSG00000181472			Zbtb2 (MGI:2685949)			
chr6	151404547	151452180	6q25	6q25.1		614917	"RMND1, COXPD11"	"Required for meiotic nuclear division 1, S. cerevisiae, homolog of"	RMND1	55005	ENSG00000155906		"Combined oxidative phosphorylation deficiency 11, 614922 (3), Autosomal recessive"	Rmnd1 (MGI:1913334)			
chr6	151452257	151470100	6q25.1	6q25.1		616332	"ARMT1, C6orf211"	Acidic residue methyltransferase 1	ARMT1	79624	ENSG00000146476			Armt1 (MGI:1920669)			
chr6	151654147	152129603	6q25.1	6q25.1-q25.2		133430	"ESR1, ESR, ESTRR"	Estrogen receptor 1	ESR1	2099	ENSG00000091831		"{Atherosclerosis, susceptibility to} (3); {Breast cancer}, 114480 (1), Autosomal dominant; Estrogen resistance, 615363 (3), Autosomal recessive; {HDL response to hormone replacement, augmented} (3); {Migraine, susceptibility to}, 157300 (3), Autosomal dominant; {Myocardial infarction, susceptibility to}, 608446 (3)"	Esr1 (MGI:1352467)			
chr6	152121683	152637398	6q25	6q25.2		608441	"SYNE1, KIAA0796, KIAA1756, KIAA1262, SCAR8, EDMD4"	Spectrin repeat-containing nuclear envelope protein 1 (nesprin 1)	SYNE1	23345	ENSG00000131018		"Emery-Dreifuss muscular dystrophy 4, autosomal dominant, 612998 (3), Autosomal dominant; Spinocerebellar ataxia, autosomal recessive 8, 610743 (3), Autosomal recessive"	Syne1 (MGI:1927152)			
chr6	152697894	152747174	6q25	6q25.2		616805	"MYCT1, MTLC"	MYC target in myeloid cells 1	MYCT1	80177	ENSG00000120279			Myct1 (MGI:1915882)			
chr6	152750796	152759764	6q26-q27	6q25.2		192320	VIP	Vasoactive intestinal peptide	VIP	7432	ENSG00000146469			Vip (MGI:98933)			
chr6	152970518	152983618	6q25-q26	6q25.2		606013	"FBXO5, FBX5, EMI1"	F-box only protein 5	FBXO5	26271	ENSG00000112029			Fbxo5 (MGI:1914391)			
chr6	154010495	154246866	6q24-q25	6q25.2		600018	OPRM1	"Opioid receptor, mu-1"	OPRM1	4988	ENSG00000112038			Oprm1 (MGI:97441)			
chr6	154405146	154510658	6q25.2	6q25.2		617476	"CNKSR3, CNK3"	"CNKSR family, member 3"	CNKSR3	154043	ENSG00000153721			Cnksr3 (MGI:2674130)			
chr6	154733377	154834243	6q25.2	6q25.2		616024	"SCAF8, KIAA1116"	SR-related C-terminal domain-associated factor 8	SCAF8	22828	ENSG00000213079			Scaf8 (MGI:1925212)			
chr6	155090288	155257722	6q25.2-q25.3	6q25.2-q25.3		604709	TIAM2	T-cell lymphoma invasion and metastasis 2	TIAM2	26230	ENSG00000146426			Tiam2 (MGI:1344338)			
chr6	155200000	160600000	6q25.3			612010	CELIAC12	"Celiac disease, susceptibility to, 12"		100188874		in LD block containing TAGAP	"{Celiac disease, susceptibility to, 12}, 612010 (2)"				
chr6	155229870	155314496	6q25	6q25.3		607033	"TFB1M, CGI75"	"Transcription factor B1, mitochondrial"	TFB1M	51106	ENSG00000029639			Tfb1m (MGI:2146851)			
chr6	155395367	155455902	6q25.1	6q25.3		607105	NOX3	NADPH oxidase 3	NOX3	50508	ENSG00000074771			Nox3 (MGI:2681162)			
chr6	156777846	157210778	6q25.1	6q25.3		614556	"ARID1B, BAF250B, KIAA1235, MRD12, CSS1"	AT-rich interaction domain-containing protein 1B	ARID1B	57492	ENSG00000049618		"Coffin-Siris syndrome 1, 135900 (3), Autosomal dominant"	Arid1b (MGI:1926129)			
chr6	157716045	157945076	6q26.3	6q25.3		605952	"SNX9, SH3PX1"	Sorting nexin 9	SNX9	51429	ENSG00000130340			Snx9 (MGI:1913866)			
chr6	157981855	158099175	6q25.3	6q25.3		609410	"SYNJ2, KIAA0348"	Synaptojanin 2	SYNJ2	8871	ENSG00000078269			Synj2 (MGI:1201671)			
chr6	158109503	158168279	6q25.3	6q25.3		614725	"SERAC1, MEGDEL"	Serine active site-containing protein 1	SERAC1	84947	ENSG00000122335		"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739 (3), Autosomal recessive"	Serac1 (MGI:2447813)			
chr6	158168315	158199343	6q25.3	6q25.3		608780	"GTF2H5, TTD3, TFB5, C6orf175, TTDA"	"General transcription factor IIH, polypeptide 5"	GTF2H5	404672	ENSG00000272047		"Trichothiodystrophy 3, photosensitive, 616395 (3)"	Gtf2h5 (MGI:107227)			
chr6	158536431	158635434	6q25.3	6q25.3		613209	"TMEM181, GPR178, KIAA1423"	Transmembrane protein 181	TMEM181	57583	ENSG00000146433			Tmem181a (MGI:1924356)			
chr6	158636473	158644785	6q25.2-q25.3	6q25.3		601554	TCTEL1	T-complex-associated-testis-expressed 1-like 1	DYNLT1	6993	ENSG00000146425			"Dynlt1c,Dynlt1b,Dynlt1a,Dynlt1f (MGI:3807476,MGI:3780996,MGI:98643,MGI:3807506)"			
chr6	158765740	158819423	6q25.3	6q25.3		123900	"EZR, VIL2, CVL"	Ezrin	EZR	7430	ENSG00000092820	coamplified with MYB		Ezr (MGI:98931)			
chr6	158947011	159000425	6q25.3	6q25.3		615876	"RSPH3, RSHL2, RSP3, CILD32"	"Radial spoke head 3, Chlamydomonas, homolog of"	RSPH3	83861	ENSG00000130363		"Ciliary dyskinesia, primary, 32, 616481 (3), Autosomal recessive"	"Rsph3a,Rsph3b (MGI:1914082,MGI:3630308)"			
chr6	159034467	159045151	6q25.3	6q25.3		609667	TAGAP	T-cell activation GTPase-activating protein	TAGAP	117289	ENSG00000164691			Tagap (MGI:3615484)			
chr6	159169396	159272107	6q25	6q25.3		609991	"FNDC1, AGS8, KIAA1866"	Fibronectin type III domain-containing protein 1	FNDC1	84624	ENSG00000164694						
chr6	159679063	159762528	6q25.3	6q25.3		147460	"SOD2, MNSOD, MVCD6"	"Superoxide dismutase-2, mitochondrial"	SOD2	6648	ENSG00000112096		"{Microvascular complications of diabetes 6}, 612634 (3)"	Sod2 (MGI:98352)			
chr6	159726695	159756318	6q25.3	6q25.3		605442	WTAP	Wilms tumor 1-associating protein	WTAP	9589	ENSG00000146457			Wtap (MGI:1926395)			
chr6	159761956	159779111	6q25.3-q26	6q25.3		100678	ACAT2	Acetyl-Coenzyme A acetyltransferase 2 (acetoacetyl Coenzyme A thiolase)	ACAT2	39	ENSG00000120437	encoded on strand opposite TCP1	"?ACAT2 deficiency, 614055 (1), Isolated cases"	"Acat3,Acat2 (MGI:109182,MGI:87871)"			
chr6	159778497	159789702	6q25.3-q26	6q25.3		186980	TCP1	T-complex locus TCP-1	TCP1	6950	ENSG00000120438	tightly linked to PLG; ~15cM proximal to TCP10; overlap with ACAT2		Tcp1 (MGI:98535)			
chr6	159789811	159798428	6q25.3	6q25.3		611831	MRPL18	Mitochondrial ribosomal protein L18	MRPL18	29074	ENSG00000112110			Mrpl18 (MGI:1914931)			
chr6	159906941	159908075	6q24-q27	6q25.3		165180	MAS1	Oncogene MAS1	MAS1	4142	ENSG00000130368			Mas1 (MGI:96918)			
chr6	159969098	160111503	6q26	6q25.3		147280	"IGF2R, MPRI"	"Insulin-like growth factor-2 receptor (mannose-6-phosphate receptor, cation-independent)"	IGF2R	3482	ENSG00000197081	behaves as a tumor suppressor	"Hepatocellular carcinoma, somatic, 114550 (3)"	Igf2r (MGI:96435)			
chr6	160003290	160007663	6q26	6q25.3		604893	"AIRN, AIR"	"Antisense IGF2R RNA, noncoding"	AIRN	100271873							
chr6	160121807	160160589	6q26	6q25.3		602607	"SLC22A1, OCT1"	"Solute carrier family 22 (organic cation transporter), member 1"	SLC22A1	6580	ENSG00000175003			Slc22a1 (MGI:108111)			
chr6	160216761	160258930	6q26	6q25.3		602608	"SLC22A2, OCT2"	"Solute carrier family 22 (organic cation transporter), member 2"	SLC22A2	6582	ENSG00000112499			Slc22a2 (MGI:1335072)			
chr6	160348372	160454981	6q27	6q25.3		604842	"SLC22A3, EMT"	"Solute carrier family 22 (extraneuronal monoamine transporter), member 3"	SLC22A3	6581	ENSG00000146477			Slc22a3 (MGI:1333817)			
chr6	160466554	160511123	6q26-q27	6q25.3		611682	"LPAL2, APOARGC"	Lipoprotein(a)-like 2	LPAL2	80350							
chr6	160531482	160666374	6q27	6q25-q26		152200	LPA	Apolipoprotein Lp(a)	LPA	4018	ENSG00000198670	absent in mice	"{Coronary artery disease, susceptibility to} (1); [LPA deficiency, congenital] (3)"				
chr6	160600000	170805979	6q26-q27			608219	DFNB38	"Deafness, autosomal recessive 38"	DFNB38	337991			"Deafness, autosomal recessive 38, 608219 (2), Autosomal recessive"				
chr6	160600000	170805979	6q26-q27			614347	MRT28	"Mental retardation, autosomal recessive 28"	MRT28	100852396		between rs6935718 and rs3886091	"Mental retardation, autosomal recessive 28, 614347 (2), Autosomal recessive"				
chr6	160702192	160754053	6q26	6q26		173350	PLG	Plasminogen	PLG	5340	ENSG00000122194	20cM from TCP10A	"Dysplasminogenemia, 217090 (3), Autosomal recessive; Plasminogen deficiency, type I, 217090 (3), Autosomal recessive"	Plg (MGI:97620)			
chr6	160991520	161117384	6q26	6q26		602425	"MAP3K4, MEKK4, MTK1, MAPKKK4"	Mitogen-activated protein kinase kinase kinase 4	MAP3K4	4216	ENSG00000085511			Map3k4 (MGI:1346875)			
chr6	161129979	161274107	6q26	6q26		614795	AGPAT4	1-acylglycerol-3-phosphate O-acyltransferase 4	AGPAT4	56895	ENSG00000026652			Agpat4 (MGI:1915512)			
chr6	161347416	162727801	6q25.2-q27	6q26		602544	"PRKN, PARK2, PDJ, LPRS2"	Parkin	PRKN	5071	ENSG00000185345	shares 5' regulatory region and both 3' UTRs with PACRG	"Adenocarcinoma of lung, somatic, 211980 (3); Adenocarcinoma, ovarian, somatic, 167000 (3); {Leprosy, susceptibility to}, 607572 (3); Parkinson disease, juvenile, type 2, 600116 (3), Autosomal recessive"	Park2 (MGI:1355296)			
chr6	162726869	163315491	6q25-q27	6q26		608427	PACRG	Parkin coregulated gene	PACRG	135138	ENSG00000112530	shares 5' regulatory region and both 3' UTRs with PARK2		Pacrg (MGI:1916560)			
chr6	163413064	163413949	6q26	6q26		615930	"CAHM, LINC00468"	"Colorectal adenocarcinoma hypermethylated gene, noncoding"	CAHM	100526820							
chr6	163414485	163578595	6q26	6q26		609590	"QKI, QK1"	"Quaking, mouse, homolog of"	QKI	9444	ENSG00000112531			Qk (MGI:97837)			
chr6	164100000	170805979	6q27			215400	CHDM	Chordoma				associated with duplication of the T gene	"{Chordoma, susceptibility to}, 215400 (4), Autosomal dominant"				
chr6	164100000	170805979	6q27			616837	HPAT5	"Human pluripotency-associated transcript 5, noncoding"									
chr6	164100000	170805979	6q27			611382	KAZA3	"Kala-azar, susceptibility to, 3"		101241899			"{Kala-azar, susceptibility to, 3}, 611382 (2)"				
chr6	165327286	165988114	6q27	6q27		610652	"PDE10A, IOLOD, ADSD2"	Phosphodiesterase 10A	PDE10A	10846	ENSG00000112541		"Dyskinesia, limb and orofacial, infantile-onset, 616921 (3), Autosomal recessive; Striatal degeneration, autosomal dominant, 616922 (3), Autosomal dominant"	Pde10a (MGI:1345143)			
chr6	166157643	166168668	6q27	6q27		601397	"T, TFT, SAVA"	"Brachyury, mouse, homolog of"	TBXT	6862	ENSG00000164458		"{Neural tube defects, susceptibility to}, 182940 (3), Autosomal dominant; Sacral agenesis with vertebral anomalies, 615709 (3), Autosomal recessive"	T (MGI:98472)			
chr6	166364918	166383012	6q27	6q27		614738	"BRP44L, MPC1, MPYCD"	Brain protein 44-like	MPC1	51660	ENSG00000060762		"Mitochondrial pyruvate carrier deficiency, 614741 (3), Autosomal recessive"	Mpc1 (MGI:1915240)			
chr6	166409363	166862550	6q27	6q27		601685	"RPS6KA2, RSK3"	"Ribosomal protein S6 kinase, 90kD, 2"	RPS6KA2	6196	ENSG00000071242			Rps6ka2 (MGI:1342290)			
chr6	166929508	166956588	6q27	6q27		612944	"RNASET2, RNASE6PL"	Ribonuclease T2	RNASET2	8635	ENSG00000026297		"Leukoencephalopathy, cystic, without megalencephaly, 612951 (3), Autosomal recessive"	"Rnaset2a,Rnaset2b (MGI:3702087,MGI:1915445)"			
chr6	166999316	167042417	6q27	6q27		605392	"FGFR1OP, FOP"	Fibroblast growth factor receptor-1 oncogene partner	FGFR1OP	11116	ENSG00000213066	"fusion gene with ZNF198, CEP1, and FGFR1"	"Myeloproliferative disorder, 605392 (2)"	Fgfr1op (MGI:1922546)			
chr6	167111806	167139140	6q27	6q27		601835	"CCR6, CMKBR6, CKRL3, GPR29, GPRCY4"	Chemokine (C-C) receptor 6	CCR6	1235	ENSG00000112486			Ccr6 (MGI:1333797)			
chr6	167156871	167157830	6q27	6q27		602043	GPR31	G protein-coupled receptor-31	GPR31	2853	ENSG00000120436			Gpr31b (MGI:1354372)			
chr6	167269031	167316013	6q27	6q27		607995	UNC93A	"UNC93, C. elegans, homolog of, A"	UNC93A	54346	ENSG00000112494			"Unc93a,Gm9992 (MGI:1933250,MGI:3712668)"			
chr6	167357355	167384545	6q27	6q27		187020	TCP10	T-complex 10 (a murine tcp homolog)	TCP10	6953	ENSG00000203690						
chr6	167826871	167972022	6q27	6q27		159559	"AFDN, MLLT4, AF6"	Afadin	AFDN	4301	ENSG00000130396			Afdn (MGI:1314653)			
chr6	167999091	168045106	6q27	6q27		603815	"KIF25, KNSL3"	Kinesin family member 25	KIF25	3834	ENSG00000125337						
chr6	168292829	168319753	6q27	6q27		608966	"DACT2, DPR2, DAPPER2"	"Dapper, antagonist of beta-catenin, 2"	DACT2	168002	ENSG00000164488			Dact2 (MGI:1920347)			
chr6	168441150	168667993	6q27	6q27		607223	"SMOC2, SMAP2, DTDP1"	Secreted modular calcium-binding protein 2	SMOC2	64094	ENSG00000112562		"Dentin dysplasia, type I, with microdontia and misshapen teeth, 125400 (3), Autosomal recessive"	Smoc2 (MGI:1929881)			
chr6	169215779	169254113	6q27	6q27		188061	THBS2	Thrombospondin 2	THBS2	7058	ENSG00000186340		"{Lumbar disc herniation, susceptibility to}, 603932 (3)"	Thbs2 (MGI:98738)			
chr6	169702111	169706357	6q27	6q27		616987	C6orf120	Chromosome 6 open reading frame 120	C6orf120	387263	ENSG00000185127			1600012H06Rik (MGI:1915162)			
chr6	169703904	169724009	6q26	6q27		613069	"PHF10, BAF45A"	PHD finger protein 10	PHF10	55274	ENSG00000130024			Phf10 (MGI:1919307)			
chr6	169725487	169751582	6q27	6q27		186977	TCTE3	T-complex-associated-testis-expressed-3	TCTE3	6991	ENSG00000184786			"Gm3448,Gm3417,Tcte3 (MGI:3809205,MGI:98642,MGI:3781595)"			
chr6	169751621	169781583	6q27	6q27		615532	"ERMARD, C6orf70, PVNH6"	Endoplasmic reticulum membrane-associated RNA degradation protein	ERMARD	55780	ENSG00000130023		"?Periventricular nodular heterotopia 6, 615544 (3), Autosomal dominant"	Ermard (MGI:1917317)			
chr6	170290702	170407747	6q26-q27	6q27		612266	"FAM120B, PGCC1, CCPG, KIAA1838"	"Family with sequence similarity 120, member B"	FAM120B	84498	ENSG00000112584			Fam120b (MGI:1914794)			
chr6	170535115	170553328	6q27	6q27		602017	PSMB1	"Proteasome subunit, beta type, 1"	PSMB1	5689	ENSG00000008018	incorrectly assigned to 7p		Psmb1 (MGI:104884)			
chr6	170554332	170572869	6q27	6q27		600075	"TBP, SCA17, HDL4"	TATA box binding protein	TBP	6908	ENSG00000112592		"{Parkinson disease, susceptibility to}, 168600 (3), Isolated cases, Multifactorial; Spinocerebellar ataxia 17, 607136 (3), Autosomal dominant"	Tbp (MGI:101838)			
chr6	170575571	170584691	6q27	6q27		600866	PDCD2	Programmed cell death 2	PDCD2	5134	ENSG00000071994			Pdcd2 (MGI:104643)			
chr6	0	170805979	Chr.6			109180	BEVI	Baboon M7 virus replication		628							
chr6	0	170805979	Chr.6			137010	FEA	F9 embryonic antigen		7959							
chr6	0	170805979	Chr.6			153435	"LAKLG, LAKL"	Lymphokine-activated killer cell ligand	LAKLG	3905							
chr6	0	170805979	Chr.6			158050	MRBC	Monkey RBC receptor		7960							
chr6	0	170805979	Chr.6			187330	TS546	"Temperature sensitivity complementation, cell cycle specific, ts546 cells"		7963							
chr7	0	43300000	7p22-p14			614021	CPVT3	"Ventricular tachycardia, catecholaminergic polymorphic, 3"				between D7S526 and D7S481	"Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021 (2), Autosomal recessive"				
chr7	0	7200000	7p22			605626	ERVK-6	"Endogenous retroviral group K, member 6"	ERVK-6	64006							
chr7	0	7200000	7p22			605635	FHII	"Hyperaldosteronism, familial, type II"		79179			"Hyperaldosteronism, familial, type II, 605635 (2)"				
chr7	0	13700000	7p22.3-p21.3			614238	HYPT10	Hypotrichosis 10		100736251		between D7S1532 and D7S3047	"Hypotrichosis 10, 614238 (2), Autosomal recessive"				
chr7	192938	260773	7p22	7p22.3		611061	"FAM20C, DMP4"	"Family with sequence similarity 20, member C"	FAM20C	56975	ENSG00000177706		"Raine syndrome, 259775 (3), Autosomal recessive"	Fam20c (MGI:2136853)			
chr7	497244	520667	7p22	7p22.3		173430	PDGFA	"Platelet-derived growth factor, alpha polypeptide"	PDGFA	5154	ENSG00000197461			Pdgfa (MGI:97527)			
chr7	549184	727675	7pter-p22	7p22.3		176911	PRKAR1B	"Protein kinase, cAMP-dependent, regulatory, type I, beta"	PRKAR1B	5575	ENSG00000188191			Prkar1b (MGI:97759)			
chr7	726691	786478	7p22.3	7p22.3		614864	"DNAAF5, HEATR2, CILD18"	Dynein axonemal assembly factor 5	DNAAF5	54919	ENSG00000164818		"Ciliary dyskinesia, primary, 18, 614874 (3), Autosomal recessive"	Dnaaf5 (MGI:3616079)			
chr7	815556	874919	7p22.3	7p22.3		607723	"UNC84A, KIAA0810, SUN1"	"UNC84, C. elegans, homolog of, A"	SUN1	23353	ENSG00000164828			Sun1 (MGI:1924303)			
chr7	876553	896433	7p22.3	7p22.3		612056	"GET4, C7orf20, CEE"	"Golgi to ER traffic protein 4, S. cerevisiae, homolog of"	GET4	51608	ENSG00000239857			Get4 (MGI:1914854)			
chr7	897899	955406	7p22.3	7p22.3		608114	CENTA1	"Centaurin, alpha-1"	ADAP1	11033	ENSG00000105963			Adap1 (MGI:2442201)			
chr7	964849	975598	7p22.3	7p22.3		610429	COX19	Cytochrome c oxidase assembly protein Cox19	COX19	90639	ENSG00000240230			Cox19 (MGI:1915283)			
chr7	983154	989639	7p22.3	7p22.3		615967	CYP2W1	"Cytochrome P450, family 2, subfamily W, polypeptide 1"	CYP2W1	54905	ENSG00000073067			Cyp2w1 (MGI:3616076)			
chr7	1022932	1023025	7p22.3	7p22.3		615977	MIR339	Micro RNA 339	MIR339	442907							
chr7	1086806	1093814	7p22	7p22.3		601805	"GPER, CMKRL2, GPR30"	G protein-coupled estrogen receptor 1	GPER1	2852	ENSG00000164850			Gper1 (MGI:1924104)			
chr7	1148849	1160218	7p22.3	7p22.3		610699	"ZFAND2A, AIRAP"	Zinc finger AN1 domain-containing protein 2A	ZFAND2A	90637	ENSG00000178381			Zfand2a (MGI:2140729)			
chr7	1470276	1504381	7p22.3	7p22.3		611345	"INTS1, INT1, KIAA1440"	Integrator complex subunit 1	INTS1	26173	ENSG00000164880			Ints1 (MGI:1915760)			
chr7	1530731	1543042	7p22	7p22.3		600197	"MAFK, NFE2U"	"V-maf avian musculoaponeurotic fibrosarcoma oncogene family, protein K (nuclear factor erythroid 2, ubiquitous subunit)"	MAFK	7975	ENSG00000198517			Mafk (MGI:99951)			
chr7	1567331	1570489	7p22.3	7p22.3		617528	"PSMG3, PAC3"	Proteasome assembly chaperone 3	PSMG3	84262	ENSG00000157778			Psmg3 (MGI:1913756)			
chr7	1666074	1747953	7p22.3	7p22.3		614964	"ELFN1, PPP1R28"	Extracellular leucine-rich repeat and fibronectin type III domain-containing protein 1	ELFN1	392617	ENSG00000225968			Elfn1 (MGI:2442479)			
chr7	1815791	2232970	7p22	7p22.3		602686	"MAD1L1, TXBP181"	"Mitotic arrest-deficient 1, yeast, homolog-like 1"	MAD1L1	8379	ENSG00000002822		"Lymphoma, somatic (3); Prostate cancer, somatic, 176807 (3)"	Mad1l1 (MGI:1341857)			
chr7	2234290	2242197	7p22	7p22.3		606906	"FTSJ2, FJH1"	"FTSJ, E. coli, homolog of, 2"	MRM2	29960	ENSG00000122687			Mrm2 (MGI:1915267)			
chr7	2242221	2251144	7p22	7p22.3		600312	"NUDT1, MTH1"	Nudix-type motif 1	NUDT1	4521	ENSG00000106268			Nudt1 (MGI:109280)			
chr7	2251769	2354476	7p22.3	7p22.3		614905	SNX8	Sorting nexin 8	SNX8	29886	ENSG00000106266			Snx8 (MGI:2443816)			
chr7	2354539	2380744	7p22.2	7p22.3		603917	"EIF3B, EIF3S9, PRT1"	"Eukaryotic translation initiation factor 3, subunit B"	EIF3B	8662	ENSG00000106263			Eif3b (MGI:106478)			
chr7	2403488	2448483	7p22	7p22.3		610129	"CHST12, C4ST2"	Carbohydrate sulfotransferase 12	CHST12	55501	ENSG00000136213			Chst12 (MGI:1929064)			
chr7	2512528	2529176	7p22	7p22.3		602576	"LFNG, SCDO3"	Lunatic fringe	LFNG	3955	ENSG00000106003	mutation identified in 1 SDO3 family	"?Spondylocostal dysostosis 3, autosomal recessive, 609813 (3)"	Lfng (MGI:1095413)			
chr7	2537809	2555757	7p22.3	7p22.3		614506	"BRAT1, BAAT1, C7orf27, RMFSL"	BRCA1-associated ATM activator 1	BRAT1	221927	ENSG00000106009		"Rigidity and multifocal seizure syndrome, lethal neonatal, 614498 (3), Autosomal recessive"	Brat1 (MGI:1891679)			
chr7	2558971	2614733	7p22.3	7p22.3		617631	"IQCE, KIAA1023, PAPA7"	IQ domain-containing protein E	IQCE	23288	ENSG00000106012	mutation identified in 1 PAPA7 family	"?Polydactyly, postaxial, type A7, 617642 (3), Autosomal recessive"	Iqce (MGI:1921489)			
chr7	2679521	2765186	7p22.3	7p22.3		615168	"AMZ1, KIAA1950"	Archaelysin family metallopeptidase 1	AMZ1	155185	ENSG00000174945			Amz1 (MGI:2442258)			
chr7	2728104	2870655	7p22.2	7p22.3-p22.2		604394	GNA12	"Guanine nucleotide-binding protein, alpha-12"	GNA12	2768	ENSG00000146535			Gna12 (MGI:95767)			
chr7	2906074	3043944	7p22	7p22.2		607210	"CARD11, CARMA1, BIMP3, PPBL, BENTA, IMD11A"	Caspase recruitment domain-containing protein 11	CARD11	84433	ENSG00000198286		"B-cell expansion with NFKB and T-cell anergy, 616452 (3), Autosomal dominant; Immunodeficiency 11A, 615206 (3), Autosomal recessive; Immunodeficiency 11B with atopic dermatitis, 617638 (3), Autosomal dominant"	Card11 (MGI:1916978)			
chr7	3301447	4268999	7p22.2	7p22.2		607216	SDK1	"Sidekick, Drosophila, homolog of, 1"	SDK1	221935	ENSG00000146555			Sdk1 (MGI:2444413)			
chr7	4500000	7200000	7p22.1			185100	STBMS1	"Strabismus, susceptibility to, 1"		100188805		max lod at marker 1911/1912	"{Strabismus, susceptibility to, 1}, 185100 (2)"				
chr7	4642283	4771442	7p22.1	7p22.1		616302	"FOXK1, MNF"	Forkhead box K1	FOXK1	221937	ENSG00000164916			Foxk1 (MGI:1347488)			
chr7	4775616	4794394	7p22.1	7p22.1		613653	"AP5Z1, KIAA0415, SPG48"	"Adaptor-related protein complex 5, zeta-1 subunit"	AP5Z1	9907	ENSG00000242802		"Spastic paraplegia 48, autosomal recessive, 613647 (3), Autosomal recessive"	Ap5z1 (MGI:1924908)			
chr7	4799108	4883703	7p22.1	7p22.1		611491	"RADIL, KIAA1849"	RAP GTPase interactor	RADIL	55698	ENSG00000157927			Radil (MGI:2443088)			
chr7	4857737	4861993	7p22.1	7p22.1		607436	"PAPOLB, TPAP"	"Poly(A) polymerase, beta"	PAPOLB	56903	ENSG00000218823			Papolb (MGI:1932115)			
chr7	4892244	4959212	7p22.1	7p22.1		614581	"MMD2, PAQR10"	Monocyte-to-macrophage differentiation-associated protein 2	MMD2	221938	ENSG00000136297			Mmd2 (MGI:1922354)			
chr7	5045820	5069487	7p22.1	7p22.1		608191	RBAK	RB-associated KRAB repressor	RBAK	57786	ENSG00000146587			Rbak (MGI:1927369)			
chr7	5190203	5233854	7p22.2	7p22.1		609225	WIPI2	WD40 repeat protein interacting with phosphoinositides 2	WIPI2	26100	ENSG00000157954			Wipi2 (MGI:1923831)			
chr7	5274310	5304072	7p22.1	7p22.1		609149	"SLC29A4, PMAT, ENT4"	"Solute carrier family 29 (monoamine transporter), member 4"	SLC29A4	222962	ENSG00000164638			Slc29a4 (MGI:2385330)			
chr7	5454447	5513797	7p22.1	7p22.1		609084	"FBXL18, FBL18"	F-box and leucine-rich repeat protein 18	FBXL18	80028	ENSG00000155034			Fbxl18 (MGI:2444450)			
chr7	5527145	5530708	7p22-p12	7p22.1		102630	"ACTB, BRWS1"	"Actin, beta"	ACTB	60	ENSG00000075624	~20 pseudogenes also; mutation identified in twin DJO patients	"Baraitser-Winter syndrome 1, 243310 (3), Autosomal dominant; ?Dystonia, juvenile-onset, 607371 (3), Autosomal dominant"	Actb (MGI:87904)			
chr7	5592804	5606655	7p22	7p22.1		602689	"FSCN1, SNL"	"Fascin homolog 1, actin-bundling protein (singed, Drosophila, homolog-like)"	FSCN1	6624	ENSG00000075618			Fscn1 (MGI:1352745)			
chr7	5620040	5781729	7p22	7p22.1		609948	"RNF216, TRIAD3, ZIN, CAHH"	RING finger protein 216	RNF216	54476	ENSG00000011275		"Cerebellar ataxia and hypogonadotropic hypogonadism, 212840 (3), Autosomal recessive"	Rnf216 (MGI:1344349)			
chr7	5859788	5886362	7p13-p11	7p22.1		164795	OCM	Oncomodulin	OCM	654231	ENSG00000122543			Ocm (MGI:97401)			
chr7	5970924	6009105	7p22	7p22.1		600259	"PMS2, PMSL2, HNPCC4"	"Postmeiotic segregation increased, S. cerevisiae, 2, homolog of"	PMS2	5395	ENSG00000122512		"Colorectal cancer, hereditary nonpolyposis, type 4, 614337 (3); Mismatch repair cancer syndrome, 276300 (3), Autosomal recessive"	Pms2 (MGI:104288)			
chr7	6009250	6023833	7p22	7p22.1		600859	"AIMP2, JTV1"	Aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	AIMP2	7965	ENSG00000106305			Aimp2 (MGI:2385237)			
chr7	6022246	6059228	7p22.1	7p22.1		613635	"EIF2AK1, HRI"	Eukaryotic translation initiation factor 2-alpha kinase 1	EIF2AK1	27102	ENSG00000086232			Eif2ak1 (MGI:1353448)			
chr7	6161778	6272610	7p22.1	7p22.1		605081	"CYTH3, PSCD3, ARNO3, GRP1"	Cytohesin 3	CYTH3	9265	ENSG00000008256			Cyth3 (MGI:1335107)			
chr7	6329408	6348958	7p22.1	7p22.1		616628	"FAM220A, SIPAR, ACPIN1, C7orf70"	"Family with sequence similarity 220, member A"	FAM220A	84792	ENSG00000178397			Fam220a (MGI:1914488)			
chr7	6374494	6403966	7p22.1	7p22.1		602048	"RAC1, MRD48"	Ras-related C3 botulinum toxin substrate 1	RAC1	5879	ENSG00000136238		"Mental retardation, autosomal dominant 48, 617751 (3), Autosomal dominant"	Rac1 (MGI:97845)			
chr7	6409115	6448011	7p22.1	7p22.1		614016	DAGLB	"Diacylglycerol lipase, beta"	DAGLB	221955	ENSG00000164535			Daglb (MGI:2442032)			
chr7	6688432	6706934	7p22-p21	7p22.1		194536	ZNF12	Zinc finger protein-12 (KOX3)	ZNF12	7559	ENSG00000164631			Zfp12 (MGI:99157)			
chr7	7182546	7248650	7p14-p13	7p22.1-p21.3		610555	C1GALT1	"Core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1"	C1GALT1	56913	ENSG00000106392			C1galt1 (MGI:2151071)			
chr7	7200000	16500000	7p21.3-p21.2			616986	LOC105375159	Long intergenic noncoding RNA AC011288.2									
chr7	7200000	28800000	7p21-p15			153880	MDDC	"Macular dystrophy, dominant cystoid"	CYMD	1541		?allelic to RP9	"Macular dystrophy, dominant cystoid, 153880 (2), Autosomal dominant"				
chr7	7338541	7542093	7p21.3	7p21.3		609996	COL28A1	"Collagen, type XXVIII, alpha-1 polypeptide"	COL28A1	340267	ENSG00000215018			Col28a1 (MGI:2685312)			
chr7	7566874	7609143	7p21.3	7p21.3		615359	MIOS	"Missing oocyte/meiosis regulator, Drosophila, homolog of"	MIOS	54468	ENSG00000164654			Mios (MGI:2182066)			
chr7	7636562	7718606	7p22	7p21.3		179837	RPA3	"Replication protein A3, 14kD"	RPA3	6119	ENSG00000106399			Rpa3 (MGI:1915490)			
chr7	7968742	8089079	7p22	7p21.3		614283	"GLCCI1, TSSN1, GCTR"	Glucocorticoid-induced transcript 1	GLCCI1	113263	ENSG00000106415		"{Glucocorticoid therapy, response to}, 614400 (3)"	Glcci1 (MGI:2179717)			
chr7	8113183	8262686	7p22	7p21.3		147625	ICA1	"Islet cell autoantigen 1, 69kD"	ICA1	3382	ENSG00000003147			Ica1 (MGI:96391)			
chr7	8433954	8752962	7p21.3	7p21.3		604639	"NXPH1, NPH1"	Neurexophilin 1	NXPH1	30010	ENSG00000122584			Nxph1 (MGI:107492)			
chr7	10931952	10940185	7p21.3	7p21.3		603833	NDUFA4	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 4"	NDUFA4	4697	ENSG00000189043			Ndufa4 (MGI:107686)			
chr7	11370434	11832197	7p21.3	7p21.3		612249	"THSD7A, KIAA0960"	Thrombospondin type-1 domain-containing protein 7A	THSD7A	221981	ENSG00000005108			Thsd7a (MGI:2685683)			
chr7	12211221	12237263	7p21.3	7p21.3		613413	TMEM106B	Transmembrane protein 106B	TMEM106B	54664	ENSG00000106460			Tmem106b (MGI:1919150)			
chr7	12570362	12653602	7p21.3	7p21.3		613416	"SCIN, KIAA1905"	Scinderin	SCIN	85477	ENSG00000006747			Scin (MGI:1306794)			
chr7	12686826	12690933	7q	7p21.3		604786	ARL4	ADP-ribosylation factor-like 4	ARL4A	10124	ENSG00000122644			Arl4a (MGI:99437)			
chr7	13700000	34900000	7p21.2-p14.3			613576	EDSS2	Ectodermal dysplasia-syndactyly syndrome 2		100505394		between D7S488 and D7S817	"Ectodermal dysplasia-syndactyly syndrome 2, 613576 (2), Autosomal recessive"				
chr7	13700000	16500000	7p21.2			613462	FGQTL4	Fasting plasma glucose level QTL 4		100499169		associated with rs2191349	"[Fasting plasma glucose level QTL 4], 613462 (2)"				
chr7	13891228	13991424	7p22	7p21.2		600541	ETV1	ETS variant gene-1	ETV1	2115	ENSG00000006468	fused with EWS in some Ewing sarcoma		Etv1 (MGI:99254)			
chr7	14145048	14974776	7p21.2	7p21.2		604070	"DGKB, DGK, KIAA0718"	"Diacylglycerol kinase, beta, 90kD"	DGKB	1607	ENSG00000136267			Dgkb (MGI:2442474)			
chr7	15117222	15562014	7p21.2	7p21.2		613738	"AGMO, TMEM195"	Alkylglycerol monooxygenase	AGMO	392636	ENSG00000187546			Agmo (MGI:2442495)			
chr7	15611211	15686682	7p22.1-p21.3	7p21.2		600535	MEOX2	Mesenchyme homeo box 2	MEOX2	4223	ENSG00000106511			Meox2 (MGI:103219)			
chr7	16087526	16502499	7p21.2	7p21.2-p21.1		614631	"ISPD, MDDGA7, MDDGC7"	Isoprenoid synthase domain-containing protein	ISPD	729920	ENSG00000214960		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, 614643 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, 616052 (3), Autosomal recessive"	Ispd (MGI:1923097)			
chr7	16461480	16465848	7p21.2	7p21.2		609675	"SOSTDC1, ECTODIN, USAG1"	Sclerostin domain-containing protein 1	SOSTDC1	25928	ENSG00000171243			Sostdc1 (MGI:1913292)			
chr7	16753725	16784535	7p21.1	7p21.1		613139	"TSPAN13, NET6"	Tetraspanin 13	TSPAN13	27075	ENSG00000106537			Tspan13 (MGI:1913359)			
chr7	16791810	16805113	7p21.3	7p21.1		606358	"AGR2, AG2"	"Anterior gradient 2, Xenopus, homolog of"	AGR2	10551	ENSG00000106541			Agr2 (MGI:1344405)			
chr7	16854710	16881988	7p21.3	7p21.1		609482	"AGR3, BCMP11"	"Anterior gradient 3, Xenopus, homolog of"	AGR3	155465	ENSG00000173467			Agr3 (MGI:2685734)			
chr7	17298651	17346150	7p15	7p21.1		600253	AHR	Aryl hydrocarbon receptor	AHR	196	ENSG00000106546			Ahr (MGI:105043)			
chr7	17790760	17940507	7p21.1	7p21.1		606589	"SNX13, KIAA0713"	Sorting nexin 13	SNX13	23161	ENSG00000071189			Snx13 (MGI:2661416)			
chr7	18026773	18027862	7p21.2	7p21.1		611566	"PRPS1L1, PRPS3"	Phosphoribosylpyrophosphate synthetase 1-like 1	PRPS1L1	221823	ENSG00000229937			Prps1l1 (MGI:1922706)			
chr7	18086941	19002415	7p21-p15	7p21.1		606543	"HDAC9, MITR, HDAC7B, KIAA0744"	Histone deacetylase 9	HDAC9	9734	ENSG00000048052			Hdac9 (MGI:1931221)			
chr7	19113046	19117671	7p21	7p21.1		601622	"TWIST1, ACS3, SCS, CRS1, SWCOS"	"TWIST, Drosophila, homolog of, 1"	TWIST1	7291	ENSG00000122691		"Craniosynostosis 1, 123100 (3), Autosomal dominant; Robinow-Sorauf syndrome, 180750 (3), Autosomal dominant; Saethre-Chotzen syndrome with or without eyelid anomalies, 101400 (3), Autosomal dominant; Sweeney-Cox syndrome, 617746 (3), Autosomal dominant"	Twist1 (MGI:98872)			
chr7	19144781	19145420	7p21.1	7p21.1		617578	"FERD3L, NTWIST, NATO3, PTFB"	"Fer3, Drosophila, homolog of"	FERD3L	222894	ENSG00000146618			Ferd3l (MGI:2150010)			
chr7	19695461	19709036	7p21	7p21.1		608312	TWISTNB	TWIST neighbor	TWISTNB	221830	ENSG00000105849	pseudogene on 6q14.3		Twistnb (MGI:106292)			
chr7	20134654	20217389	7p21.1	7p21.1		612646	MACC1	Metastasis-associated gene in colon cancer 1	MACC1	346389	ENSG00000183742			Macc1 (MGI:2685113)			
chr7	20615621	20757013	7p15.3	7p21.1		611785	ABCB5	"ATP-binding cassette, subfamily B, member 5"	ABCB5	340273	ENSG00000004846			Abcb5 (MGI:1924956)			
chr7	20782273	20786888	7p21	7p21.1		608306	"SP8, BTD"	Transcription factor Sp8	SP8	221833	ENSG00000164651			Sp8 (MGI:2443471)			
chr7	20900000	45400000	7p15-p13			613219	"FGQTL2, BWQTL1"	Fasting plasma glucose level QTL 2; Birth weight QTL 1		100379216		associated with rs4607517	"[Birth weight QTL 1], 613219 (2); [Fasting plasma glucose level QTL 2], 613219 (2)"				
chr7	20900000	28800000	7p15			164865	MYCLK1	Avian myelocytomatosis viral (v-myc) oncogene homolog like 1									
chr7	20900000	28800000	7p15			608367	"MYP17, MYP4"	Myopia 17	MYP17	100359401		previously assigned to 7q36 (MYP4)	"Myopia 17, 608367 (2), Autosomal dominant"				
chr7	20900000	28800000	7p15			612737	STQTL17	Stature quantitative trait locus 17		100301526		associated with rs1635852 and rs849140	"{Stature QTL 17}, 612737 (2)"				
chr7	21428033	21514821	7p15	7p15.3		600540	SP4	Sp4 transcription factor	SP4	6671	ENSG00000105866			Sp4 (MGI:107595)			
chr7	21543214	21901567	7p21	7p15.3		603339	"DNAH11, DNAHC11, CILD7, DNAHBL"	"Dynein, axonemal, heavy chain-11"	DNAH11	8701	ENSG00000105877		"Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3), Autosomal recessive"	Dnah11 (MGI:1100864)			
chr7	21900898	21945923	7p15	7p15.3		609685	"CDCA7L, R1, JPO2"	Cell division cycle-associated protein 7-like	CDCA7L	55536	ENSG00000164649			Cdca7l (MGI:2384982)			
chr7	22725888	22732001	7p21	7p15.3		147620	"IL6, IFNB2, BSF2, HSF, HGF"	"Interleukin-6 (interferon, beta-2)"	IL6	3569	ENSG00000136244		"{Crohn disease-associated growth failure}, 266600 (3), Multifactorial; {Diabetes, susceptibility to},, 222100 (3), Autosomal recessive; {Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to}, 108010 (3), Autosomal dominant; {Kaposi sarcoma, susceptibility to}, 148000 (3), Autosomal dominant; {Rheumatoid arthritis, systemic juvenile}, 604302 (3)"	Il6 (MGI:96559)			
chr7	22812631	22822851	7p15.3	7p15.3		607980	TOMM7	"Translocase of outer mitochondrial membrane 7, yeast, homolog of"	TOMM7	54543	ENSG00000196683			Tomm7 (MGI:1913419)			
chr7	22895847	23014150	7p15.3	7p15.3		610531	"FAM126A, DRCTNNB1A, HLD5"	Hyccin	FAM126A	84668	ENSG00000122591		"Leukodystrophy, hypomyelinating, 5, 610532 (3), Autosomal recessive"	Fam126a (MGI:2149839)			
chr7	23105733	23175420	7p15.3	7p15.3		611119	"KLHL7, RP42, CISS3"	Kelch-like 7	KLHL7	55975	ENSG00000122550		"Cold-induced sweating syndrome 3, 617055 (3), Autosomal recessive; Retinitis pigmentosa 42, 612943 (3), Autosomal dominant"	Klhl7 (MGI:1196453)			
chr7	23246696	23275109	7p15.3	7p15.3		604368	"GPNMB, PLCA3"	Glycoprotein NMB	GPNMB	10457	ENSG00000136235		"Amyloidosis, primary localized cutaneous, 3, 617920 (3), Autosomal recessive"	Gpnmb (MGI:1934765)			
chr7	23298743	23309572	7p15.3	7p15.3		614624	"MALSU1, C7orf30"	Mitochondrial assembly of ribosomal large subunit 1	MALSU1	115416	ENSG00000156928			Malsu1 (MGI:1922843)			
chr7	23310208	23470673	7p15	7p15.3		608259	"IGF2BP3, IMP3, KOC1, VICKZ3"	Insulin-like growth factor 2 mRNA-binding protein 3	IGF2BP3	10643	ENSG00000136231			Igf2bp3 (MGI:1890359)			
chr7	23504779	23532040	7p15.3	7p15.3		602718	TRA2A	"Transformer 2, Drosophila, homolog of"	TRA2A	29896	ENSG00000164548			Tra2a (MGI:1933972)			
chr7	23710139	23832514	7p15.3	7p15.3		605790	STK31	Serine/threonine kinase 31	STK31	56164	ENSG00000196335			Stk31 (MGI:1924735)			
chr7	24284187	24291864	7p15.1	7p15.3		162640	NPY	Neuropeptide Y	NPY	4852	ENSG00000122585			Npy (MGI:97374)			
chr7	24573345	24694085	7p21-p15	7p15.3		606959	"MPP6, VAM1, PALS2"	"Membrane protein, palmitoylated 6"	MPP6	51678	ENSG00000105926			Mpp6 (MGI:1927340)			
chr7	24698354	24762234	7p15	7p15.3		608798	"GSDME, DFNA5"	Gasdermin E	GSDME	1687	ENSG00000105928		"Deafness, autosomal dominant 5, 600994 (3), Autosomal dominant"	Gsdme (MGI:1889850)			
chr7	24796536	24980217	7p15	7p15.3		606732	"OSBPL3, ORP3, KIAA0704"	Oxysterol-binding protein-like protein 3	OSBPL3	26031	ENSG00000070882			Osbpl3 (MGI:1918970)			
chr7	25118650	25125360	7p15.2	7p15.3		123970	"CYCS, CYC, THC4"	"Cytochrome C, somatic"	CYCS	54205	ENSG00000172115		"Thrombocytopenia 4, 612004 (3), Autosomal dominant"	Cycs (MGI:88578)			
chr7	25134696	25180741	7p15.3	7p15.3		616071	C7orf31	Chromosome 7 open reading frame 31	C7orf31	136895	ENSG00000153790			4921507P07Rik (MGI:1918071)			
chr7	25224569	25228485	7p15.3	7p15.3		616984	"NPVF, RFRP, C7orf9"	Neuropeptide VF precursor	NPVF	64111	ENSG00000105954			Npvf (MGI:1926488)			
chr7	25949918	25949985	7p15.2	7p15.2		613786	"MIR148A, MIRN148A"	Micro RNA 148A	MIR148A	406940							
chr7	26152226	26187136	7p15-p14	7p15.2		604135	"NFE2L3, NRF3"	Nuclear factor erythroid 2-like 3	NFE2L3	9603	ENSG00000050344			Nfe2l3 (MGI:1339958)			
chr7	26189919	26200792	7p15	7p15.2		600124	"HNRPA2B1, IBMPFD2"	Heterogeneous nuclear ribonucleoprotein A2/B1	HNRNPA2B1	3181	ENSG00000122566	mutation identified in 1 family	"?Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2, 615422 (3)"	Hnrnpa2b1 (MGI:104819)			
chr7	26201210	26213606	7p15.2	7p15.2		604477	CBX3	Chromobox homolog 3	CBX3	11335	ENSG00000122565			Cbx3 (MGI:108515)			
chr7	26291894	26374329	7p15.2	7p15.2		614780	"SNX10, OPTB8"	Sorting nexin 10	SNX10	29887	ENSG00000086300		"Osteopetrosis, autosomal recessive 8, 615085 (3), Autosomal recessive"	Snx10 (MGI:1919232)			
chr7	26654771	26864742	7p15.2	7p15.2		605215	"SKAP2, SCAP2, SKAP55R"	src kinase associated phosphoprotein 2	SKAP2	8935	ENSG00000005020			Skap2 (MGI:1889206)			
chr7	27092992	27096005	7p15.3	7p15.2		142955	"HOXA1, HOX1F, BSAS"	Homeo box-A1	HOXA1	3198	ENSG00000105991		"Athabaskan brainstem dysgenesis syndrome, 601536 (3); Bosley-Salih-Alorainy syndrome, 601536 (3)"	Hoxa1 (MGI:96170)			
chr7	27100353	27102774	7p15-p14	7p15.2		604685	"HOXA2, MCOHI"	Homeobox A2	HOXA2	3199	ENSG00000105996		"?Microtia with or without hearing impairment (AD), 612290 (3), Autosomal recessive, Autosomal dominant; ?Microtia, hearing impairment, and cleft palate (AR), 612290 (3), Autosomal recessive, Autosomal dominant"	Hoxa2 (MGI:96174)			
chr7	27106189	27153237	7p15-p14.2	7p15.2		142954	"HOXA3, HOX1E"	Homeo box-A3	HOXA3	3200	ENSG00000105997	"homolog of Drosophila zen1, zen2"		Hoxa3 (MGI:96175)			
chr7	27121918	27128759	7p15.2	7p15.2		616068	HOXAAS2	HOXA cluster antisense RNA 2	HOXA-AS2	285943							
chr7	27128506	27130779	7p15-p14.2	7p15.2		142953	"HOXA4, HOX1D"	Homeo box-A4	HOXA4	3201	ENSG00000197576	homolog of Drosophila Dfd		Hoxa4 (MGI:96176)			
chr7	27141051	27143667	7p15-p14.2	7p15.2		142952	"HOXA5, HOX1C"	Homeo box-A5	HOXA5	3202	ENSG00000106004			Hoxa5 (MGI:96177)			
chr7	27145582	27147773	7p15-p14.2	7p15.2		142951	"HOXA6, HOX1B"	Homeo box-A6	HOXA6	3203	ENSG00000106006			Hoxa6 (MGI:96178)			
chr7	27153715	27156676	7p15-p14.2	7p15.2		142950	"HOXA7, HOX1A"	Homeo box-A7	HOXA7	3204	ENSG00000122592	homolog of Drosophila Antp		Hoxa7 (MGI:96179)			
chr7	27162437	27165529	7p15-p14.2	7p15.2		142956	"HOXA9, HOX1G"	Homeo box-A9	HOXA9	3205	ENSG00000078399	homolog of Drosophila Abd-B; fused to NUP98 in myeloid leukemia		Hoxa9 (MGI:96180)			
chr7	27169479	27169562	7p15-p14.2	7p15.2		609688	"MIR196B, MIRN196B"	Micro RNA 196B	MIR196B	442920							
chr7	27170590	27180260	7p15-p14.2	7p15.2		142957	"HOXA10, HOX1H"	Homeo box-A10	HOXA10	3206	ENSG00000253293			Hoxa10 (MGI:96171)			
chr7	27181156	27185215	7p15-p14.2	7p15.2		142958	"HOXA11, HOX1I, RUSAT1"	Homeo box-A11	HOXA11	3207	ENSG00000005073		"Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, 605432 (3), Autosomal dominant"	Hoxa11 (MGI:96172)			
chr7	27185407	27189292	7p15.2	7p15.2		607530	HOXA11AS	"Homeo box A11, antisense"	HOXA11-AS	221883							
chr7	27196879	27200105	7p15-p14.2	7p15.2		142959	"HOXA13, HOX1J"	Homeo box-A13	HOXA13	3209	ENSG00000106031		"Guttmacher syndrome, 176305 (3), Autosomal dominant; Hand-foot-uterus syndrome, 140000 (3), Autosomal dominant"	Hoxa13 (MGI:96173)			
chr7	27200420	27207258	7p15.2	7p15.2		614060	"HOTTIP, NCRNA00213"	HOXA distal transcript antisense RNA	HOTTIP	100316868							
chr7	27242544	27247818	7p15-p14	7p15.2		142996	EVX1	Even-skipped homeo box-1 (homolog of Drosophila)	EVX1	2128	ENSG00000106038	at 5' end of HOX1 cluster		Evx1 (MGI:95461)			
chr7	27525439	27663000	7p15.2	7p15.2		608475	HIBADH	3-hydroxyisobutyrate dehydrogenase	HIBADH	11112	ENSG00000106049			Hibadh (MGI:1889802)			
chr7	27739372	27829766	7p15	7p15.2		605326	"TAX1BP1, TXBP151"	TAX1-binding protein 1	TAX1BP1	8887	ENSG00000106052			Tax1bp1 (MGI:1289308)			
chr7	27830572	28180817	7p15	7p15.2-p15.1		606246	"JAZF1, TIP27"	JAZF1 gene	JAZF1	221895	ENSG00000153814	fused with JJAZ1		Jazf1 (MGI:2141450)			
chr7	28800000	43300000	7p14			610655	HHT4	"Telangiectasia, hereditary hemorrhagic, type 4"		791087		between D7S2252 and D7S510	"Telangiectasia, hereditary hemorrhagic, type 4, 610655 (2), Autosomal dominant"				
chr7	28953357	28958412	7p14.3	7p14.3		613356	"TRIL, KIAA0644"	TLR4 interactor with leucine-rich repeats	TRIL	9865	ENSG00000255690			Tril (MGI:1914123)			
chr7	28995230	29195450	7p15-p14	7p14.3		609780	"CPVL, HVLP"	"Carboxypeptidase, vitellogenic-like"	CPVL	54504	ENSG00000106066			Cpvl (MGI:1918537)			
chr7	29146546	29514334	7p15.3	7p14.3		602857	"CHN2, ARHGAP3, RHOGAP3"	"Chimerin 2 (GTPase-activating protein, rho, 3)"	CHN2	1124	ENSG00000106069			Chn2 (MGI:1917243)			
chr7	29806553	29917065	7p15.1	7p14.3		612432	"WIPF3, CR16"	"WAS/WASL-interacting protein family, member 3"	WIPF3	644150	ENSG00000122574			Wipf3 (MGI:3044681)			
chr7	29920102	29990288	7p14.3-p14.1	7p14.3		614965	"SCRN1, SES1, KIAA0193"	Secernin 1	SCRN1	9805	ENSG00000136193			Scrn1 (MGI:1917188)			
chr7	30010582	30026800	7p15.1	7p14.3		614505	"FKBP14, EDSKSCL2"	FK506-binding protein 14	FKBP14	55033	ENSG00000106080		"Ehlers-Danlos syndrome, kyphoscoliotic type, 2, 614557 (3), Autosomal recessive"	Fkbp14 (MGI:2387639)			
chr7	30028360	30130482	7p21-p11.2	7p14.3		608639	FAPP2	Phosphatidylinositol 4-phosphate adaptor protein 2	PLEKHA8	84725	ENSG00000106086			Plekha8 (MGI:2681164)			
chr7	30284306	30367691	7p15.1	7p14.3		612061	ZNRF2	Zinc finger and ring finger protein 2	ZNRF2	223082	ENSG00000180233			Znrf2 (MGI:1196246)			
chr7	30424526	30478865	7p15-p14	7p14.3		605980	"NOD1, CARD4"	Nucleotide-binding oligomerization domain protein 1	NOD1	10392	ENSG00000106100			Nod1 (MGI:1341839)			
chr7	30496620	30504840	7p15-p14	7p14.3		137170	"GGCT, GCTG, C7orf24"	Gamma-glutamylcyclotransferase	GGCT	79017	ENSG00000006625			Ggct (MGI:95700)			
chr7	30594734	30634032	7p15	7p14.3		600287	"GARS, SMAD1, CMT2D, HMN5"	Glycyl-tRNA synthetase	GARS	2617	ENSG00000106105		"Charcot-Marie-Tooth disease, type 2D, 601472 (3), Autosomal dominant; Neuropathy, distal hereditary motor, type VA, 600794 (3), Autosomal dominant"	Gars (MGI:2449057)			
chr7	30649405	30700102	7p21-p15	7p14.3		602034	"CRHR2, CRFR2"	Corticotropin releasing hormone receptor-2	CRHR2	1395	ENSG00000106113			Crhr2 (MGI:894312)			
chr7	30752134	30757601	7p15.3-p15.2	7p14.3		604854	INMT	Indolethylamine N-methyltransferase	INMT	11185	ENSG00000241644			Inmt (MGI:102963)			
chr7	30911693	30925516	7p14	7p14.3		107776	"AQP1, CHIP28, CO"	"Aquaporin-1 (channel-forming integral protein, 28kD)"	AQP1	358	ENSG00000240583		"[Aquaporin-1 deficiency], 110450 (3); [Blood group, Colton], 110450 (3)"	Aqp1 (MGI:103201)			
chr7	30964020	30979530	7p15-p14	7p14.3		139191	"GHRHR, GHRFR, IGHD1B"	Growth hormone releasing hormone receptor	GHRHR	2692	ENSG00000106128		"Growth hormone deficiency, isolated, type IB, 612781 (3)"	Ghrhr (MGI:95710)			
chr7	31052340	31111478	7p14	7p14.3		102981	"ADCYAP1R1, PACAPR"	Adenylate cyclase activating polypeptide-1 (pituitary) receptor type 1	ADCYAP1R1	117	ENSG00000078549			Adcyap1r1 (MGI:108449)			
chr7	31337460	31340923	7p15-p14	7p14.3		611513	"NEUROD6, ATOH2, MATH2"	Neurogenic differentiation 6	NEUROD6	63974	ENSG00000164600			Neurod6 (MGI:106593)			
chr7	31616776	32428223	7p14.3	7p14.3		602987	"PDE1C, HCAM3"	Phosphodiesterase 1C	PDE1C	5137	ENSG00000154678			Pde1c (MGI:108413)			
chr7	31687016	31710157	7p15	7p14.3		604088	GSBS	G-substrate	PPP1R17	10842	ENSG00000106341		"{Hypercholesterolemia, susceptibility to}, 143890 (3), Autosomal dominant"	Ppp1r17 (MGI:1333876)			
chr7	32485332	32495257	7p14.3	7p14.3		607285	LSM5	LSM5 protein	LSM5	23658	ENSG00000106355			Lsm5 (MGI:1913623)			
chr7	32495425	32588740	7p14.3	7p14.3		612927	"AVL9, KIAA0241"	"AVL9, S. cerevisiae, homolog of"	AVL9	23080	ENSG00000105778			Avl9 (MGI:1926187)			
chr7	32957403	33006930	7p12	7p14.3		616257	"FKBP9, FKBP60, FKBP63"	FK506-binding protein 9	FKBP9	11328	ENSG00000122642			Fkbp9 (MGI:1350921)			
chr7	33014112	33062820	7p15-p14	7p14.3		606224	"NT5C3A, NT5C3, UMPH1, PSN1"	"5' nucleotidase, cytosolic IIIA (uridine 5' monophosphate hydrolase 1)"	NT5C3A	51251	ENSG00000122643	pseudogenes on chr.4 and chr.7	"Anemia, hemolytic, due to UMPH1 deficiency, 266120 (3), Autosomal recessive"	Nt5c3 (MGI:1927186)			
chr7	33094796	33109389	7p14.2	7p14.3		607331	"RP9, PAP1"	"RP9 gene (pim1-associated protein, mouse, homolog of)"	RP9	6100	ENSG00000164610	mutation identified in 1 patient	"?Retinitis pigmentosa 9, 180104 (3), Autosomal dominant"	Rp9 (MGI:2157166)			
chr7	33129243	33637237	7p14	7p14.3		607968	"PTHB1, BBS9"	Parathyroid hormone-responsive B1 gene	BBS9	27241	ENSG00000122507		"Bardet-Biedl syndrome 9, 615986 (3), Autosomal recessive"	Bbs9 (MGI:2442833)			
chr7	33904910	34155871	7p14.3	7p14.3		608699	"BMPER, CV2"	BMP binding endothelial regulator	BMPER	168667	ENSG00000164619		"Diaphanospondylodysostosis, 608022 (3), Autosomal recessive"	Bmper (MGI:1920480)			
chr7	34346511	34834330	7p15-p14	7p14.3		608596	AAA1	Asthma-associated alternatively spliced gene 1	NPSR1-AS1	404744							
chr7	34658238	34878331	7p15-p14	7p14.3		608595	"NPSR1, GPR154, GPRA, VRR1, PGR14, ASRT2"	Neuropeptide S receptor 1	NPSR1	387129	ENSG00000187258		"{Asthma, susceptibility to, 2}, 608584 (3)"	Npsr1 (MGI:2441738)			
chr7	34928880	35038040	7p14.3	7p14.2		613892	"DPY19L1, KIAA0877"	DPY19-like 1	DPY19L1	23333	ENSG00000173852			Dpy19l1 (MGI:1915685)			
chr7	35199935	35254099	7p15-p14	7p14.2		606061	"TBX20, ASD4"	T-box 20	TBX20	57057	ENSG00000164532		"Atrial septal defect 4, 611363 (3)"	Tbx20 (MGI:1888496)			
chr7	35800985	35915762	7p14	7p14.2		603151	"SEPT7, CDC10"	Septin 7	7-Sep	989	ENSG00000122545			Sept7 (MGI:1335094)			
chr7	36153226	36301542	7p14.2	7p14.2		617192	"EEPD1, KIAA1706"	Endonuclease/exonuclease/phosphatase family domain-containing protein 1	EEPD1	80820	ENSG00000122547			Eepd1 (MGI:1914734)			
chr7	36389802	36453790	7p14.2	7p14.2		616027	"ANLN, FSFS8"	Actin-binding protein anillin	ANLN	54443	ENSG00000011426		"Focal segmental glomerulosclerosis 8, 616032 (3), Autosomal dominant"	Anln (MGI:1920174)			
chr7	36509312	36724548	7p14-p12	7p14.2		102593	AOAH	Acyloxyacyl hydrolase (neutrophil)	AOAH	313	ENSG00000136250			Aoah (MGI:1350928)			
chr7	36852905	37449325	7p14	7p14.2-p14.1		606420	"ELMO1, CED12"	Engulfment and cell motility gene 1	ELMO1	9844	ENSG00000155849			Elmo1 (MGI:2153044)			
chr7	37100000	43300000	7p14.1			615455	TRGJ@	T-cell receptor gamma chain joining gene cluster									
chr7	37100000	43300000	7p14.1			615454	TRGV@	T-cell receptor gamma chain variable gene cluster									
chr7	37683559	37743834	7p14.1	7p14.1		609045	"GPR141, PGR13"	G protein -coupled receptor 141	GPR141	353345	ENSG00000187037			Gpr141 (MGI:2672983)			
chr7	37848596	37900400	7p14.1	7p14.1		607421	"NME8, TXNDC3, SPTRX2, CILD6"	NME/NM23 family member 8	NME8	51314	ENSG00000086288		"Ciliary dyskinesia, primary, 6, 610852 (3), Autosomal recessive"	Nme8 (MGI:1920662)			
chr7	37905931	37916922	7p14.1	7p14.1		606570	"SFRP4, FRPHE, PYL"	Secreted frizzled-related protein 4	SFRP4	6424	ENSG00000106483		"Pyle disease, 265900 (3), Autosomal recessive"	Sfrp4 (MGI:892010)			
chr7	38178205	38230670	7p14-p13	7p14.1		611759	"STARD3NL, MENTHO"	STARD3 N-terminal like	STARD3NL	83930	ENSG00000010270			Stard3nl (MGI:1923455)			
chr7	38239576	38276740	7p15-p14	7p14.1		609642	TARP	"T-cell antigen receptor, gamma subunit, alternate reading frame protein"		445347	ENSG00000211689						
chr7	38240023	38249571	7p14.1	7p14.1		615450	TRGC2	T-cell receptor gamma chain constant region 2	TRGC2	6967							
chr7	38260087	38265677	7p14.1	7p14.1		186970	TRGC1	T-cell receptor gamma chain constant region 1	TRGC1	6966							
chr7	38383693	38631566	7p14-p13	7p14.1		600418	AMPH	Amphiphysin	AMPH	273	ENSG00000078053			Amph (MGI:103574)			
chr7	38722974	38909199	7p14.1	7p14.1		605485	VPS41	"Vacuolar protein sorting 41, Yeast, homolog of"	VPS41	27072	ENSG00000006715			Vps41 (MGI:1929215)			
chr7	38977877	39468600	7p14-p13	7p14.1		609062	"POU6F2, WTSL, WT5"	"POU domain, class 6, transcription factor 2"	POU6F2	11281	ENSG00000106536		"{Wilms tumor susceptibility-5}, 601583 (3), Autosomal dominant, Somatic mutation"				
chr7	39622954	39708123	7p22-p15	7p14.1		179550	RALA	"RAS-like protein A (Simian leukemia viral (v-ral) oncogene homolog A, ras-related)"	RALA	5898	ENSG00000006451			Rala (MGI:1927243)			
chr7	39949663	40097133	7p14.1	7p14.1		603309	"CDK13, CDC2L5, CHED, CHDFIDD"	Cyclin-dependent kinase 13	CDK13	8621	ENSG00000065883		"Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360 (3), Autosomal dominant"	Cdk13 (MGI:1916812)			
chr7	40132742	40134651	7p14	7p14.1		609188	"MPLKIP, C7orf11, ABHS, TTDN1, TTD4"	M-phase specific PLK1 interacting protein	MPLKIP	136647	ENSG00000168303		"Trichothiodystrophy 4, nonphotosensitive, 234050 (3), Autosomal recessive"	Mplkip (MGI:1913558)			
chr7	40134886	40860766	7p14	7p14.1		609187	"C7orf10, GA3"	Chromosome 7 open reading frame 10	SUGCT	79783	ENSG00000175600		"Glutaric aciduria III, 231690 (3), Autosomal recessive"	Sugct (MGI:1923221)			
chr7	41685100	41710531	7p15-p13	7p14.1		147290	INHBA	"Inhibin, beta-1"	INHBA	3624	ENSG00000122641			Inhba (MGI:96570)			
chr7	41960948	42237018	7p13	7p14.1		165240	"GLI3, PAPA, PAPB"	GLI-Kruppel family member GLI3 (oncogene GLI3)	GLI3	2737	ENSG00000106571	amplified in glioblastoma	"Greig cephalopolysyndactyly syndrome, 175700 (3), Autosomal dominant; {Hypothalamic hamartomas, somatic}, 241800 (3); Pallister-Hall syndrome, 146510 (3), Autosomal dominant; Polydactyly, postaxial, types A1 and B, 174200 (3), Autosomal dominant; Polydactyly, preaxial, type IV, 174700 (3), Autosomal dominant"	Gli3 (MGI:95729)			
chr7	42916860	42932205	7p13	7p14.1		176842	"PSMA2, PSC2, HC3"	"Proteasome (prosome, macropain) subunit, alpha type, 2"	PSMA2	5683	ENSG00000106588	incorrectly assigned to 6q		Psma2 (MGI:104885)			
chr7	42932339	42937856	7p14	7p14.1		611839	MRPL32	Mitochondrial ribosomal protein L32	MRPL32	64983	ENSG00000106591			Mrpl32 (MGI:2137226)			
chr7	43112579	43566000	7p13	7p14-p13		610384	"HECW1, NEDL1, KIAA0322"	"HECT, C2, and WW domains-containing E3 ubiquitin-protein ligase 1"	HECW1	23072	ENSG00000002746			Hecw1 (MGI:2444115)			
chr7	43583092	43627378	7p13	7p13		604726	"STK17A, DRAK1"	Serine/threonine protein kinase 17A	STK17A	9263	ENSG00000164543						
chr7	43608451	43729540	7p13	7p13		614769	"COA1, C7orf44"	"Cytochrome c oxidase assembly factor 1, S. cerevisiae, homolog of"	COA1	55744	ENSG00000106603						
chr7	43758121	43807341	7p13	7p13		109750	BLVRA	Biliverdin reductase A	BLVRA	644	ENSG00000106605		"Hyperbiliverdinemia, 614156 (3), Autosomal recessive, Autosomal dominant"	Blvra (MGI:88170)			
chr7	43866557	43869545	7p14	7p13		611986	MRPS24	Mitochondrial ribosomal protein S24	MRPS24	64951	ENSG00000062582			Mrps24 (MGI:1928142)			
chr7	43875893	43926410	7p13	7p13		610337	"URGCP, URG4"	Upregulator of cell proliferation	URGCP	55665	ENSG00000106608			Urgcp (MGI:1919296)			
chr7	43997854	44011039	7p13	7p13		617623	"SPDYE1, SPDYB2L2, RINGO1"	"SPEEDY/RINGO cell cycle regulator family, member E1"	SPDYE1	285955	ENSG00000136206						
chr7	44044639	44061912	7p13	7p13		610106	"DBNL, HIP55"	Drebrin-like	DBNL	28988	ENSG00000136279			Dbnl (MGI:700006)			
chr7	44062726	44065586	7p13-p12.3	7p13		612931	"PGAM2, PGAMM, GSD10"	"Phosphoglycerate mutase, muscle form"	PGAM2	5224	ENSG00000164708		"Glycogen storage disease X, 261670 (3), Autosomal recessive"	Pgam2 (MGI:1933118)			
chr7	44072061	44082539	7p13	7p13		606344	POLM	"Polymerase, DNA, mu"	POLM	27434	ENSG00000122678			Polm (MGI:1860191)			
chr7	44114679	44123667	7p13	7p13		600815	POLD2	"Polymerase (DNA directed), delta 2, regulatory subunit, 50kD"	POLD2	5425	ENSG00000106628			Pold2 (MGI:1097163)			
chr7	44138863	44141391	7p13	7p13		613993	"MYL7, MYL2A, MLC2A, MYLC2A"	"Myosin, light chain 7, regulatory"	MYL7	58498	ENSG00000106631			Myl7 (MGI:107495)			
chr7	44143212	44189438	7p15-p13	7p13		138079	"GCK, HHF3"	Glucokinase (hexokinase-4)	GCK	2645	ENSG00000106633	proximal to TCRB	"Diabetes mellitus, noninsulin-dependent, late onset, 125853 (3), Autosomal dominant; Diabetes mellitus, permanent neonatal, 606176 (3), Autosomal recessive, Autosomal dominant; Hyperinsulinemic hypoglycemia, familial, 3, 602485 (3), Autosomal dominant; MODY, type II, 125851 (3), Autosomal dominant"	Gck (MGI:1270854)			
chr7	44217149	44326166	7p14	7p13		607707	"CAMK2B, MRD54"	Calcium/calmodulin-dependent protein kinase II-beta	CAMK2B	816	ENSG00000058404		"Mental retardation, autosomal dominant 54, 617799 (3), Autosomal dominant"	Camk2b (MGI:88257)			
chr7	44382365	44490874	7p13	7p13		610296	"NUDCD3, KIAA1068, NUDCL"	NUDC domain-containing protein 3	NUDCD3	23386	ENSG00000015676			Nudcd3 (MGI:2144158)			
chr7	44512439	44541650	7p13	7p13		608010	NPC1L1	NPC1-like 1	NPC1L1	29881	ENSG00000015520		"[Ezetimibe, nonresponse to] (3)"	Npc1l1 (MGI:2685089)			
chr7	44565416	44574537	7p13	7p13		608023	"DDX56, NOH61"	DEAD/H box 56	DDX56	54606	ENSG00000136271			Ddx56 (MGI:1277172)			
chr7	44577893	44582294	7p22.2	7p13		612038	TMED4	Transmembrane p24 trafficking protein 4	TMED4	222068	ENSG00000158604			Tmed4 (MGI:1915070)			
chr7	44606521	44709069	7p14-p13	7p13		613022	OGDH	"Oxoglutarate dehydrogenase, lipoamide (alpha-ketoglutarate dehydrogenase)"	OGDH	4967	ENSG00000105953		"Alpha-ketoglutarate dehydrogenase deficiency, 203740 (1), Autosomal recessive"	Ogdh (MGI:1098267)			
chr7	44748546	44769880	7p13	7p13		611196	"ZMIZ2, KIAA1886, ZIMP7"	Zinc finger MIZ-domain containing 2	ZMIZ2	83637	ENSG00000122515			Zmiz2 (MGI:106374)			
chr7	44795959	44803122	7p13	7p13		123840	PPIA	Peptidylprolyl isomerase A (cyclophilin A)	PPIA	5478	ENSG00000196262			Ppia (MGI:97749)			
chr7	44876292	44885384	7p13	7p13		608887	PURB	Purine-rich element-binding protein B	PURB	5814	ENSG00000146676			Purb (MGI:1338779)			
chr7	44962660	44979104	7p13	7p13		600642	"MYO1G, HA2, HLA-HA2"	Myosin IG	MYO1G	64005	ENSG00000136286			Myo1g (MGI:1927091)			
chr7	44999745	45076469	7p13	7p13		607929	"C7orf22, CCM2, MGC4067"	Malcavernin	CCM2	83605	ENSG00000136280		"Cerebral cavernous malformations-2, 603284 (3), Autosomal dominant"	Ccm2 (MGI:2384924)			
chr7	45100099	45111746	7p13	7p13		611325	"TBRG4, KIAA0948, CPR2"	Transforming growth factor-beta regulator 4	TBRG4	9238	ENSG00000136270			Tbrg4 (MGI:1100868)			
chr7	45104905	45105041	7p13	7p13		611335	SNORA5C	"Small nucleolar RNA, H/ACA box, 5C"	SNORA5C	677796		in intron 3 of TBRG4					
chr7	45157767	45184249	7p13-p12	7p13		605155	RAMP3	Receptor activity-modifying protein 3	RAMP3	10268	ENSG00000122679			Ramp3 (MGI:1860292)			
chr7	45400000	60100000	7p12-cen			147830	TTIM1	"T-cell tumor invasion and metastasis-1 (invasion-metastasis of neoplasms, chromosome 7 determined)"									
chr7	45574139	45723115	7p13-p12	7p12.3		103072	"ADCY1, DFNB44"	"Adenylate cyclase-1, brain"	ADCY1	107	ENSG00000164742	mutation identified in 1 DFNB44 family	"?Deafness, autosomal recessive 44, 610154 (3), Autosomal recessive"	Adcy1 (MGI:99677)			
chr7	45723786	45769017	7p13	7p12.3		611563	13-Sep	Septin 13	SEPT7P2	641977							
chr7	45888418	45893667	7p14-p12	7p12.3		146730	IGFBP1	Insulin-like growth factor-binding protein-1	IGFBP1	3484	ENSG00000146678			Igfbp1 (MGI:96436)			
chr7	45912244	45921271	7p14-p12	7p12.3		146732	IGFBP3	Insulin-like growth factor-binding protein-3	IGFBP3	3486	ENSG00000146674	tail-to-tail 20kb from IGFBP1		Igfbp3 (MGI:96438)			
chr7	47275153	47582552	7p12.3	7p12.3		606825	"TNS3, TEM6"	Tensin 3	TNS3	64759	ENSG00000136205			Tns3 (MGI:2443012)			
chr7	47774602	47958912	7p13-p12	7p12.3		609721	"PKD1L1, HTX8"	Polycystin 1L1	PKD1L1	168507	ENSG00000158683		"Heterotaxy, visceral, 8, autosomal, 617205 (3), Autosomal recessive"	Pkd1l1 (MGI:2156538)			
chr7	47962979	47979624	7p13-p12	7p12.3		603760	HUS1	"Hydroxyurea-sensitive 1, S. pombe, homolog of"	HUS1	3364	ENSG00000136273			Hus1 (MGI:1277962)			
chr7	48088307	48108745	7p12.3	7p12.3		191730	"UPP1, UP"	Uridine phosphorylase 1	UPP1	7378	ENSG00000183696			Upp1 (MGI:1097668)			
chr7	48171423	48647496	7p12.3	7p12.3		607807	ABCA13	"ATP-binding cassette, subfamily A, member 13"	ABCA13	154664	ENSG00000179869			Abca13 (MGI:2388707)			
chr7	49000000	50500000	7p12.2			613067	ALL2	"Leukemia, acute lymphoblastic, susceptibility to, 2"		100310786		associated with rs11978267	"{Leukemia, acute lymphoblastic, susceptibility to, 2}, 613067 (2)"				
chr7	49773660	49923776	7p12.2	7p12.2		611108	"VWC2, BRORIN"	von Willebrand factor C domain-containing protein 2	VWC2	375567	ENSG00000188730			Vwc2 (MGI:2442987)			
chr7	49846354	50093263	7p12.2	7p12.2		608498	"ZPBP, SP38"	Zona pellucida-binding protein	ZPBP	11055	ENSG00000042813			Zpbp (MGI:1855701)			
chr7	50303452	50405100	7p12	7p12.2		603023	"IKZF1, ZNFN1A1, IK1, LYF1, CVID13"	Ikaros family zinc finger 1	IKZF1	10320	ENSG00000185811	fused with BCL6 in DLBL	"Immunodeficiency, common variable, 13, 616873 (3), Autosomal dominant"	Ikzf1 (MGI:1342540)			
chr7	50437319	50450405	7p12.1	7p12.2		615383	FIGNL1	Fidgetin-like protein 1	FIGNL1	63979	ENSG00000132436			Fignl1 (MGI:1890648)			
chr7	50458435	50565459	7p11	7p12.2-p12.1		107930	DDC	DOPA decarboxylase (aromatic L-amino acid decarboxylase)	DDC	1644	ENSG00000132437		"Aromatic L-amino acid decarboxylase deficiency, 608643 (3), Autosomal recessive"	Ddc (MGI:94876)			
chr7	50500000	98400000	7p12.1-q21			614676	CMH21	"Cardiomyopathy, familial hypertrophic, 21"		100909387		max lod at D7S669	"Cardiomyopathy, hypertrophic, 21, 614676 (2), Autosomal dominant"				
chr7	50590062	50793461	7p12-p11.2	7p12.1		601523	"GRB10, RSS"	Growth factor receptor-bound protein-10	GRB10	2887	ENSG00000106070			Grb10 (MGI:103232)			
chr7	51016211	51316860	7p12	7p12.1		610317	"COBL, KIAA0633"	"Cordon-bleu, mouse, homolog of"	COBL	23242	ENSG00000106078			Cobl (MGI:105056)			
chr7	53900000	98400000	7p11-q21			608658	HPC4	"Prostate cancer, hereditary, 4"		408260			"{Prostate cancer, susceptibility to, 4}, 176807 (2), Autosomal dominant"				
chr7	53900000	58100000	7p11.2			608345	NYS3	"Nystagmus 3, congenital, autosomal dominant"	NYS3	4934		translocation t(7;15)(p11.2;q11.2)	"Nystagmus 3, congenital, autosomal dominant, 608345 (2), Autosomal dominant"				
chr7	53900000	58100000	7p11.2			180860	"SRS, RSS"	Silver-Russell syndrome				maternal uniparental disomy of chromosome 7	"Silver-Russell syndrome, 180860 (4), Isolated cases"				
chr7	54201223	54202420	7p14-p13	7p11.2		600762	"HPVC1, PE5L"	Human papillomavirus E5 central sequence-like 1	HPVC1	3262							
chr7	54752246	54759245	7p11.2	7p11.2		609215	SEC61G	"Sec61 complex, gamma subunit"	SEC61G	23480	ENSG00000132432			"Gm16261,Sec61g,Gm11575,Gm12881,Gm4184 (MGI:3782360,MGI:3649592,MGI:3651892,MGI:3826544,MGI:1202066)"			
chr7	55019020	55208079	7p12.3-p12.1	7p11.2		131550	"EGFR, NISBD2"	Epidermal growth factor receptor	EGFR	1956	ENSG00000146648	same as oncogene ERBB; mutation identified in 1 NISBD2 family	"Adenocarcinoma of lung, response to tyrosine kinase inhibitor in, 211980 (3), Autosomal recessive; ?Inflammatory skin and bowel disease, neonatal, 2, 616069 (3), Autosomal recessive; Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, 211980 (3), Autosomal recessive; {Nonsmall cell lung cancer, susceptibility to}, 211980 (3), Autosomal recessive"	Egfr (MGI:95294)			
chr7	55365447	55433741	7p11.2	7p11.2		612919	"LANCL2, TASP"	LanC-like 2	LANCL2	55915	ENSG00000132434			Lancl2 (MGI:1919085)			
chr7	55434405	55572519	7p11.2	7p11.2		611915	"VOPP1, ECOP, GASP"	"Vesicular, overexpressed in cancer, prosurvival protein 1"	VOPP1	81552	ENSG00000154978			Vopp1 (MGI:2141658)			
chr7	55764796	55773695	7q11.2	7p11.2		604239	"PSPHP1, PSPHL, CO9"	Phosphoserine phosphatase-like (pseudogene)	PSPHP1	8781							
chr7	55793543	55862788	7p11.2	7p11.2		612140	14-Sep	Septin 14	14-Sep	346288	ENSG00000154997			Sept14 (MGI:1921472)			
chr7	55887276	55942224	7p11.2	7p11.2		616181	ZNF713	Zinc finger protein 713	ZNF713	349075	ENSG00000178665						
chr7	55951917	55955340	7p11-q11.21	7p11.2		611980	MRPS17	Mitochondrial ribosomal protein S17	MRPS17	51373	ENSG00000239789	9 pseudogenes		Mrps17 (MGI:1913508)			
chr7	55964576	56000181	7p12	7p11.2		603004	"GBAS, NIPSNAP2"	Glioblastoma amplified sequence	NIPSNAP2	2631	ENSG00000146729			Nipsnap2 (MGI:1278343)			
chr7	56010486	56051603	7p11.2	7p11.2		172480	"PSPH, PSP, PSPHD"	Phosphoserine phosphatase	PSPH	5723	ENSG00000146733		"Phosphoserine phosphatase deficiency, 614023 (3), Autosomal recessive"	Psph (MGI:97788)			
chr7	56051684	56063988	7p11.2	7p11.2		104613	"CCT6A, CCT6, HTR3, TCP20"	"Chaperonin containing T-complex polypeptide 1, subunit 6A"	CCT6A	908	ENSG00000146731			Cct6a (MGI:107943)			
chr7	56064006	56080671	7p11.2	7p11.2		607940	SUMF2	Sulfatase-modifying factor 2	SUMF2	25870	ENSG00000129103			Sumf2 (MGI:1915152)			
chr7	56079926	56093449	7p12-q21	7p11.2		172470	PHKG1	"Phosphorylase kinase, gamma 1, muscle"	PHKG1	5260	ENSG00000164776	presumed pseudogene on 11		Phkg1 (MGI:97579)			
chr7	56101561	56106629	7p11.2	7p11.2		616244	"CHCHD2, PARK22"	Coiled-coil-helix-coiled-coil-helix domain-containing protein 2	CHCHD2	51142	ENSG00000106153		"Parkinson disease 22, autosomal dominant, 616710 (3), Autosomal dominant"	"Chchd2,Chchd2-ps (MGI:1261428,MGI:3649942)"			
chr7	57119573	57139898	7p11.2	7p11.2		617444	"ZNF479, KR19"	Zinc finger protein 479	ZNF479	90827	ENSG00000185177						
chr7	60100000	159345973	7q			145290	HRX	Hyperreflexia		7974		linked to KEL					
chr7	60100000	159345973	7q			252270	"MLSM7, DEL7q, C7DELq"	Monosomy 7 of bone marrow					"Myelodysplasia and leukemia syndrome with monosomy 7, 252270 (4), Autosomal recessive"				
chr7	62100000	77900000	7q11.2			105800	ANIB1	"Aneurysm, intracranial berry, 1"	ANIB1	116833		in or near ELN	"Aneurysm, intracranial berry, 1, 105800 (2), Autosomal dominant"				
chr7	62100000	98400000	7q11.2-q21.3			129900	EEC1	"Ectrodactyly, ectodermal dysplasia, cleft lip/palate, 1"	EEC1	1913			"?EEC syndrome-1, 129900 (2), Autosomal dominant"				
chr7	62100000	77900000	7q11.2			610247	"EOE1, EE"	"Esophagitis, eosinophilic, 1"		100302511		associated with rs2302009	"{Esophagitis, eosinophilic, 1}, 610247 (2), Multifactorial"				
chr7	64665009	64711581	7q11.2	7q11.21		603989	ZNF107	Zinc finger protein-107	ZNF107	51427	ENSG00000196247						
chr7	64794387	64853799	7q11.21-q11.23	7q11.21		604080	ZNF138	Zinc finger protein-138	ZNF138	7697	ENSG00000197008						
chr7	64882492	64932238	7q11.21	7q11.21		604756	"ZNF273, HZF9"	Zinc finger protein 273	ZNF273	10793	ENSG00000198039						
chr7	64974451	64991035	7q11.2	7q11.21		194624	ZNF117	Zinc finger protein-117	ZNF117	51351	ENSG00000152926						
chr7	64990354	65006745	7q11.2	7q11.21		131170	ERV3	Endogenous retroviral sequence-3 (includes zinc finger protein H-plk)	ERV3-1	2086	ENSG00000213462						
chr7	65373798	65401134	7q11.21	7q11.21		603974	ZNF92	Zinc finger protein-92	ZNF92	168374	ENSG00000146757	sequence aligns with sequence on 19p13.1-p12					
chr7	65865771	65959562	7q11.21	7q11.21		608838	VKORC1L1	"Vitamin K epoxide reductase complex, subunit 1-like 1"	VKORC1L1	154807	ENSG00000196715			Vkorc1l1 (MGI:1916818)			
chr7	65960683	65982313	7q21.11	7q11.21		611499	"GUSB, MPS7"	"Glucuronidase, beta-"	GUSB	2990	ENSG00000169919		"Mucopolysaccharidosis VII, 253220 (3), Autosomal recessive"	Gusb (MGI:95872)			
chr7	66075788	66093342	7cen-q11.2	7q11.21		608310	ASL	Argininosuccinate lyase	ASL	435	ENSG00000126522		"Argininosuccinic aciduria, 207900 (3), Autosomal recessive"	Asl (MGI:88084)			
chr7	66114817	66154567	7q21.3-q22	7q11.21		606121	RCP	Calcitonin gene-related peptide receptor component protein	CRCP	27297	ENSG00000241258			Crcp (MGI:1100818)			
chr7	66205271	66360450	7q11.21	7q11.21		603125	TPST1	Tyrosylprotein sulfotransferase 1	TPST1	8460	ENSG00000169902			Tpst1 (MGI:1298231)			
chr7	66628880	66643228	7q11.21	7q11.21		611725	"KCTD7, EPM3, CLN14"	Potassium channel tetramerization domain containing 7	KCTD7	154881	ENSG00000243335		"Epilepsy, progressive myoclonic 3, with or without intracellular inclusions, 611726 (3), Autosomal recessive"	Kctd7 (MGI:2442265)			
chr7	66682090	66811463	7q11.21	7q11.21		609700	"RABGEF1, RABEX5"	RAB guanine nucleotide exchange factor 1	RABGEF1	27342	ENSG00000154710			Rabgef1 (MGI:1929459)			
chr7	66987676	66995695	7q11	7q11.21		607444	"SBDS, SDS"	SBDS gene	SBDS	51119	ENSG00000126524		"{Aplastic anemia, susceptibility to}, 609135 (3); Shwachman-Diamond syndrome, 260400 (3), Autosomal recessive"	Sbds (MGI:1913961)			
chr7	66996804	67239519	7q11.21	7q11.21		611243	TYW1	"tRNA-wybutosine-synthesizing protein 1, S. cerevisiae, homolog of"	TYW1	55253	ENSG00000198874			Tyw1 (MGI:2141161)			
chr7	69598474	70793067	7q11.2	7q11.22		607270	"KIAA0442, MRD26"	KIAA0442 gene	AUTS2	26053	ENSG00000158321	translocation break at 7q11.2	"Mental retardation, autosomal dominant 26, 615834 (3), Autosomal dominant"	Auts2 (MGI:1919847)			
chr7	71132404	71713600	7q11.22	7q11.22		615137	"WBSCR17, GALNTL3, GALNACT17"	Williams-Beuren syndrome chromosome region 17	GALNT17	64409	ENSG00000185274			Galnt17 (MGI:2137594)			
chr7	72700000	77900000	7q11.23			613729	"DEL7q11.23, C7DELq11.23"	"Chromosome 7q11.23 deletion syndrome, distal, 1.2Mb"				contiguous gene deletion syndrome	"Chromosome 7q11.23 deletion syndrome, distal, 1.2Mb, 613729 (4)"				
chr7	72700000	77900000	7q11.23			609757	"DUP7q11.23, C7DUPq11.23"	Chromosome 7q11.23 duplication syndrome					"Chromosome 7q11.23 duplication syndrome, 609757 (4), Autosomal dominant"				
chr7	72700000	77900000	7q11.23			194050	"WBS, WMS, WS, DEL7q11, C7DELq11"	Williams-Beuren syndrome (chromosome 7q11.23 deletion syndrome)				contiguous gene syndrome	"Williams-Beuren syndrome, 194050 (4), Autosomal dominant"				
chr7	72879334	72951439	7q11.23	7q11.23		615753	"POM121, POM121A, KIAA0618"	POM121 transmembrane nucleoporin	POM121	9883	ENSG00000196313			Pom121 (MGI:2137624)			
chr7	72954844	73005931	7q11.23	7q11.23		612550	"TRIM74, TRIM50C"	Tripartite motif-containing protein 74	TRIM74	378108	ENSG00000155428						
chr7	73302515	73308866	7q11.23	7q11.23		615732	"NSUN5, WBSCR20, WBSCR20A"	"NOP2/SUN RNA methyltransferase family, member 5"	NSUN5	55695	ENSG00000130305			Nsun5 (MGI:2140844)			
chr7	73312535	73328081	7q11.23	7q11.23		612548	"TRIM50, TRIM50A"	Tripartite motif-containing protein 50	TRIM50	135892	ENSG00000146755			Trim50 (MGI:2664992)			
chr7	73328151	73358636	7q11.23	7q11.23		604839	FKBP6	FK506-binding protein 6	FKBP6	8468	ENSG00000077800			Fkbp6 (MGI:2137612)			
chr7	73433778	73436119	7q11.23	7q11.23		601766	"FZD9, FZD3"	"Frizzled, Drosophila, homolog of, 9"	FZD9	8326	ENSG00000188763			Fzd9 (MGI:1313278)			
chr7	73440397	73522284	7q11-q21	7q11.23		605681	"BAZ1B, WSTF, WBSCR9"	"Bromodomain adjacent to zinc finger domain, 1B"	BAZ1B	9031	ENSG00000009954			Baz1b (MGI:1353499)			
chr7	73536352	73557734	7q11.23	7q11.23		605846	BCL7B	B-cell CLL/lymphoma 7B	BCL7B	9275	ENSG00000106635			Bcl7b (MGI:1332238)			
chr7	73568943	73578682	7q11.23	7q11.23		605842	TBL2	Transducin-beta-like 2	TBL2	26608	ENSG00000106638			Tbl2 (MGI:1351652)			
chr7	73593193	73624542	7q11.23	7q11.23		605678	"MLXIPL, WBSCR14, MONDOB, CHREBP"	MLX interacting protein-like	MLXIPL	51085	ENSG00000009950			Mlxipl (MGI:1927999)			
chr7	73665345	73672109	7q11.23	7q11.23		610039	"VPS37D, WBSCR24"	"Vacuolar protein sorting 37, yeast, homolog of, D"	VPS37D	155382	ENSG00000176428			Vps37d (MGI:2159402)			
chr7	73683567	73698220	7q11.23	7q11.23		615733	"BUD23, WBSCR22, MERM1"	rRNA methyltransferase and ribosome maturation factor Bud23	BUD23	114049	ENSG00000071462			Bud23 (MGI:1913388)			
chr7	73699204	73719686	7q11.2	7q11.23		186590	"STX1A, STX1"	"Syntaxin 1A, brain"	STX1A	6804	ENSG00000106089			Stx1a (MGI:109355)			
chr7	73735068	73735999	7q11.23	7q11.23		612545	WBSCR26	Williams-Beuren syndrome chromosome region 26	ABHD11-AS1	171022							
chr7	73768996	73770269	7q11	7q11.23		602910	"CLDN3, CPETR2"	Claudin-3 (Clostridium perfringens enterotoxin receptor 2)	CLDN3	1365	ENSG00000165215			Cldn3 (MGI:1329044)			
chr7	73830862	73832692	7q11.23	7q11.23		602909	"CLDN4, CPETR1, CPER"	Claudin 4	CLDN4	1364	ENSG00000189143			Cldn4 (MGI:1313314)			
chr7	73834589	73842526	7q11.23	7q11.23		612546	WBSCR27	Williams-Beuren syndrome chromosome region 27	METTL27	155368	ENSG00000165171			Mettl27 (MGI:1933146)			
chr7	73860847	73865892	7q11.23	7q11.23		612547	WBSCR28	Williams-Beuren syndrome chromosome region 28	TMEM270	135886	ENSG00000175877			Tmem270 (MGI:1923879)			
chr7	74027771	74069906	7q11.2	7q11.23		130160	"ELN, SVAS, ADCL1"	Elastin	ELN	2006	ENSG00000049540		"Cutis laxa, autosomal dominant, 123700 (3), Autosomal dominant; Supravalvar aortic stenosis, 185500 (3), Autosomal dominant"				
chr7	74083776	74122524	7q11.23	7q11.23		601329	LIMK1	LIM domain kinase 1	LIMK1	3984	ENSG00000106683			Limk1 (MGI:104572)			
chr7	74174375	74197100	7q11.23	7q11.23		603431	"EIF4H, WBSCR1, WSCR1"	Eukaryotic translation initiation factor 4H	EIF4H	7458	ENSG00000106682			Eif4h (MGI:1341822)			
chr7	74191197	74191293	7q11.23	7q11.23		615070	MIR590	Micro RNA 590	MIR590	693175							
chr7	74209756	74229833	7q11.23	7q11.23		605719	"LAT2, WBSCR5, LAB, NTAL"	"Linker for activation of T cells family, member 2"	LAT2	7462	ENSG00000086730			Lat2 (MGI:1926479)			
chr7	74231501	74254457	7q11.23	7q11.23		600404	RFC2	"Replication factor C2, 40kD (activator 1, 40kD)"	RFC2	5982	ENSG00000049541			Rfc2 (MGI:1341868)			
chr7	74289436	74405942	7q11.23	7q11.23		603432	"CLIP2, CYLN2, WBSCR4, WSCR4"	CAP-GLY domain-containing linker protein 2	CLIP2	7461	ENSG00000106665	?neurodevelopmental defect of Williams syndrome		Clip2 (MGI:1313136)			
chr7	74453789	74603069	7q11.23	7q11.23		604318	"GTF2IRD1, GTF3, MUSTRD1, WBS"	GTF21 repeat domain-containing protein 1	GTF2IRD1	9569	ENSG00000006704			Gtf2ird1 (MGI:1861942)			
chr7	74657664	74760691	7q11.23	7q11.23		601679	"GTF2I, BAP135, WBS"	"General transcription factor II-I (BTK-associated protein, 135kD)"	GTF2I	2969	ENSG00000263001			Gtf2i (MGI:1202722)			
chr7	74773961	74789375	7q11.23	7q11.23		608512	NCF1	"Neutrophil cytosolic factor-1, 47kD"	NCF1	653361	ENSG00000158517		"Chronic granulomatous disease due to deficiency of NCF-1, 233700 (3), Autosomal recessive"	Ncf1 (MGI:97283)			
chr7	74964692	75031531	7q11.23	7q11.23		617033	"GATSL2, CASTOR2"	GATS protein-like 2	CASTOR2	729438	ENSG00000274070			Gatsl2 (MGI:1933384)			
chr7	75395628	75405612	7q11.23	7q11.23		612549	"TRIM73, TRIM50B"	Tripartite motif-containing protein 73	TRIM73	375593	ENSG00000178809						
chr7	75416780	75486287	7q11.23	7q11.23		615754	"POM121C, POM121-2"	POM121 Transmembrane nucleoporin C	POM121C	100101267	ENSG00000272391			Pom121 (MGI:2137624)			
chr7	75533297	75738975	7q11.23	7q11.23		601767	HIP1	Huntingtin interacting protein-1	HIP1	3092	ENSG00000127946		"{Prostate cancer, progression of}, 176807 (1), Autosomal dominant"	Hip1 (MGI:1099804)			
chr7	75769523	75791582	7q11.2	7q11.23		604697	"CCL26, SCYA26"	"Chemokine, C-C motif, ligand 26"	CCL26	10344	ENSG00000006606						
chr7	75810824	75823355	7q11.23	7q11.23		602495	"CCL24, SCYA24, MPIF2"	"Chemokine, C-C motif, ligand 24"	CCL24	6369	ENSG00000106178			Ccl24 (MGI:1928953)			
chr7	75878991	75888925	7q11.23	7q11.23		615203	RHBDD2	Rhomboid domain-containing protein 2	RHBDD2	57414	ENSG00000005486			Rhbdd2 (MGI:1915612)			
chr7	75915101	75986854	7q11.2	7q11.23		124015	POR	Cytochrome P450 oxidoreductase	POR	5447	ENSG00000127948		"Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3), Autosomal recessive; Disordered steroidogenesis due to cytochrome P450 oxidoreductase, 613571 (3)"	Por (MGI:97744)			
chr7	75986836	75994673	7q11.23	7q11.23		616550	"TMEM120A, TMPIT, NET29"	Transmembrane protein 120A	TMEM120A	83862	ENSG00000189077			Tmem120a (MGI:2686991)			
chr7	75995819	76049343	7q11.23	7q11.23		616695	"STYXL1, MKSTYX, DUSP24"	Serine/threonine/tyrosine-interacting protein-like 1	STYXL1	51657	ENSG00000127952			Styxl1 (MGI:1923821)			
chr7	76048018	76067507	7q11.23	7q11.23		154100	"MDH2, EIEE51"	"Malate dehydrogenase, mitochondrial"	MDH2	4191	ENSG00000146701		"Epileptic encephalopathy, early infantile, 51, 617339 (3), Autosomal recessive"	Mdh2 (MGI:97050)			
chr7	76302557	76304300	7q11.23	7q11.23		602195	"HSPB1, HSP27, CMT2F, HMN2B"	Heat-shock 27kD protein-1	HSPB1	3315	ENSG00000106211		"Charcot-Marie-Tooth disease, axonal, type 2F, 606595 (3), Autosomal dominant; Neuropathy, distal hereditary motor, type IIB, 608634 (3), Autosomal dominant"	Hspb1 (MGI:96240)			
chr7	76326790	76359024	7q11.23	7q11.23		605356	"YWHAG, EIEE56"	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma isoform"	YWHAG	7532	ENSG00000170027		"Epileptic encephalopathy, early infantile, 56, 617665 (3), Autosomal dominant"	Ywhag (MGI:108109)			
chr7	76389328	76410024	7q11.23	7q11.23		607639	SRCRB4D	Protein with 4 group B scavenger receptor cysteine-rich domains	SSC4D	136853	ENSG00000146700			Ssc4d (MGI:1924709)			
chr7	76397523	76442070	7q11.23	7q11.23		182889	"ZP3, ZP3A, ZP3B, OOMD3"	Zona pellucida glycoprotein-3 (sperm receptor)	ZP3	7784	ENSG00000188372		"Oocyte maturation defect 3, 617712 (3), Autosomal dominant"	Zp3 (MGI:99215)			
chr7	76461654	76505994	7q11.23	7q11.23		613141	"DTX2, KIAA1528"	"Deltex, Drosophila, homolog of, 2"	DTX2	113878	ENSG00000091073			Dtx2 (MGI:1921448)			
chr7	76510341	76516520	7q11.23	7q11.23		611887	"UPK3B, UPIIIB, P35"	Uroplakin 3B	UPK3B	105375355	ENSG00000243566						
chr7	76609985	76627302	7q11.2	7q11.23		600587	POMZP3	POM121/ZP3 fusion protein	POMZP3	22932	ENSG00000146707						
chr7	77193370	77199832	7q11.2	7q11.23		605351	FGL2	Fibrinogen-like 2	FGL2	10875	ENSG00000127951			Fgl2 (MGI:103266)			
chr7	77310750	77416418	7q11.23	7q11.23		613552	"GSAP, PION"	Gamma-secretase-activating protein	GSAP	54103	ENSG00000186088			Gsap (MGI:2442259)			
chr7	77537189	77640070	7q11.23	7q11.23		600079	"PTPN12, PTPG1"	"Protein tyrosine phosphatase, nonreceptor-type, 12"	PTPN12	5782	ENSG00000127947		"Colon cancer, somatic, 114500 (3)"	Ptpn12 (MGI:104673)			
chr7	77657659	77697344	7q21	7q11.23		616048	APTR	"Alu-mediated CDKN1A/p21 transcriptional regulator, noncoding"	APTR	100505854							
chr7	77798791	77957503	7q11.23-q21	7q11.23-q21.11		616785	PHTF2	Putative homeodomain transcription factor 2	PHTF2	57157	ENSG00000006576			Phtf2 (MGI:1916020)			
chr7	77900000	98400000	7q21			608950	"MAGI2IT, PR47"	MAGI2 intronic transcript									
chr7	77900000	107800000	7q21-q22			154276	MHS3	Malignant hyperthermia susceptibility 3		7977		?mutation in CACNA2	"{Malignant hyperthermia susceptibility 3}, 154276 (2), Autosomal dominant"				
chr7	77900000	98400000	7q21			612223	STQTL11	Stature quantitative trait locus 11		100270795		associated with rs2282978	"{Stature QTL 11}, 612223 (2)"				
chr7	78017054	79453573	7q21	7q21.11		606382	"MAGI2, AIP1, KIAA0705"	"Membrane-associated guanylate kinase, WW and PDZ domains-containing, 2"	MAGI2	9863	ENSG00000187391		"Nephrotic syndrome 15, 617609 (3), Autosomal recessive"	Magi2 (MGI:1354953)			
chr7	80134823	80219408	7q21	7q21.11		139310	GNAI1	"Guanine nucleotide-binding protein (G protein), alpha-inhibiting activity polypeptide-1"	GNAI1	2770	ENSG00000127955			Gnai1 (MGI:95771)			
chr7	80457290	80512502	7q21.11	7q21.11		139395	"GNAT3, GDCA"	"Guanine nucleotide-binding protein, alpha-transducing activity polypeptide 3"	GNAT3	346562	ENSG00000214415			Gnat3 (MGI:3588268)			
chr7	80602187	80679276	7q21.11	7q21.11		173510	"CD36, CHDS7, BDPLT10"	CD36 antigen (collagen type I)	CD36	948	ENSG00000135218		"{Coronary heart disease, susceptibility to, 7}, 610938 (3); [Macrothrombocytopenia] (1); {Malaria, cerebral, reduced risk of}, 611162 (3); {Malaria, cerebral, susceptibility to}, 611162 (3); Platelet glycoprotein IV deficiency, 608404 (3), Autosomal recessive"	Cd36 (MGI:107899)			
chr7	80742535	80922378	7q21.11	7q21.11		602645	SEMA3C	Semaphorin 3C	SEMA3C	10512	ENSG00000075223			Sema3c (MGI:107557)			
chr7	81699005	81770437	7q21.1	7q21.11		142409	"HGF, DFNB39"	Hepatic growth factor	HGF	3082	ENSG00000019991		"Deafness, autosomal recessive 39, 608265 (3), Autosomal recessive"	Hgf (MGI:96079)			
chr7	81946443	82443805	7q21-q22	7q21.11		114204	"CACNA2, CACNL2A"	"Calcium channel, voltage-dependent, L type, alpha 2/delta subunit"	CACNA2D1	781	ENSG00000153956			Cacna2d1 (MGI:88295)			
chr7	82754004	83164160	7q11.23-q21.1	7q21.11		604918	"PCLO, PCH3"	"Piccolo, mouse, homolog of"	PCLO	27445	ENSG00000186472	mutation identified in 1 PCHD3 family	"?Pontocerebellar hypoplasia, type 3, 608027 (3), Autosomal recessive"	Pclo (MGI:1349390)			
chr7	83363905	83649162	7q21.11	7q21.11		608166	"SEMA3E, SEMAH, KIAA0331"	Semaphorin 3E	SEMA3E	9723	ENSG00000170381	mutation identified in 1 CHARGE patient	"?CHARGE syndrome, 214800 (3), Autosomal dominant"	Sema3e (MGI:1340034)			
chr7	83956845	84515188	7q21.11	7q21.11		603961	"SEMA3A, SEMAD, COLL1, HH16"	Semaphorin 3A	SEMA3A	10371	ENSG00000075213		"{Hypogonadotropic hypogonadism 16 with or without anosmia}, 614897 (3), Autosomal dominant"	Sema3a (MGI:107558)			
chr7	84995191	85187175	7q21.11	7q21.11		609907	SEMA3D	Semaphorin 3D	SEMA3D	223117	ENSG00000153993			Sema3d (MGI:1860118)			
chr7	86643913	86864878	7q21.1-q21.2	7q21.11-q21.12		601115	GRM3	"Glutamate receptor, metabotropic-3"	GRM3	2913	ENSG00000198822			Grm3 (MGI:1351340)			
chr7	86876905	87059713	7q21.12	7q21.12		614048	"KIAA1324L, EIG121L"	KIAA1324-like gene	KIAA1324L	222223	ENSG00000164659			9330182L06Rik (MGI:2443264)			
chr7	87152360	87196331	7q21.12	7q21.12		608491	"DMTF1, DMP1"	Cyclin D-binding MYB-like transcription factor 1	DMTF1	9988	ENSG00000135164			Dmtf1 (MGI:1344415)			
chr7	87196161	87220586	7q21.12	7q21.12		616993	"TMEM243, C7orf23, MMTRAG"	Transmembrane protein 243	TMEM243	79161	ENSG00000135185			Tmem243 (MGI:3606159)			
chr7	87325346	87345491	7q21.12	7q21.12		616403	TP53TG1	TP53 target gene 1	TP53TG1	11257							
chr7	87345634	87399795	7q21.1	7q21.12		606090	"CROT, COT"	Carnitine octanoyltransferase	CROT	54677	ENSG00000005469			Crot (MGI:1921364)			
chr7	87398987	87476721	7q21.1	7q21.12		171060	"ABCB4, PGY3, MDR3, ICP3"	"ATP-binding cassette, subfamily B, member 4 (P-glycoprotein-3/multiple drug resistance-3)"	ABCB4	5244	ENSG00000005471	within 500kb of MDR1	"Cholestasis, intrahepatic, of pregnancy, 3, 614972 (3), Autosomal recessive, Autosomal dominant; Cholestasis, progressive familial intrahepatic 3, 602347 (3), Autosomal recessive; Gallbladder disease 1, 600803 (3), Autosomal recessive, Autosomal dominant"	Abcb4 (MGI:97569)			
chr7	87503862	87713322	7q21.1	7q21.12		171050	"ABCB1, PGY1, MDR1, IBD13, CLCs"	"ATP-binding cassette, subfamily B, member 1 (P-glycoprotein-1/multiple drug resistance-1)"	ABCB1	5243	ENSG00000085563		"{Colchicine resistance}, 120080 (3); {Inflammatory bowel disease 13}, 612244 (3)"	Abcb1a (MGI:97570)			
chr7	87627655	87832297	7q21.12	7q21.12		617295	"RUNDC3B, RPIP9"	RUN domain-containing protein 3B	RUNDC3B	154661	ENSG00000105784			Rundc3b (MGI:2685286)			
chr7	87834498	87876376	7q21.12	7q21.12		610821	SLC25A40	"Solute carrier family 25, member 40"	SLC25A40	55972	ENSG00000075303			Slc25a40 (MGI:2442486)			
chr7	87876228	87909540	7q21.3	7q21.12		604281	"ASK, DBF4"	Activator of S-phase kinase	DBF4	10926	ENSG00000006634			Dbf4 (MGI:1351328)			
chr7	87934142	88202888	7q21	7q21.12		603709	ADAM22	A disintegrin and metalloproteinase domain 22	ADAM22	53616	ENSG00000008277			Adam22 (MGI:1340046)			
chr7	88205114	88226992	7q21.1	7q21.12		182520	"SRI, SCN"	Sorcin (class 4 gene)	SRI	6717	ENSG00000075142			Sri (MGI:98419)			
chr7	88276428	88306912	7q21	7q21.12		611098	"STEAP4, STAMP2, TIARP"	Six-transmembrane epithelial antigen of prostate 4	STEAP4	79689	ENSG00000127954			Steap4 (MGI:1923560)			
chr7	90154374	90164826	7q21	7q21.13		604415	STEAP	Six-transmembrane epithelial antigen of the prostate	STEAP1	26872	ENSG00000164647			Steap1 (MGI:1917608)			
chr7	90211685	90243407	7q21	7q21.13		605094	"STEAP2, STAMP1, IPCA1, PCANAP1"	Six-transmembrane epithelial antigen of prostate 2	STEAP2	261729	ENSG00000157214			Steap2 (MGI:1921301)			
chr7	90346664	90391454	7q21.13	7q21.13		610920	"GTPBP10, OBGH2"	GTP-binding protein 10	GTPBP10	85865	ENSG00000105793			Gtpbp10 (MGI:2385599)			
chr7	90403333	90415953	7q21	7q21.13		611232	CLKDN12	Claudin 12	CLDN12	9069	ENSG00000157224			Cldn12 (MGI:1929288)			
chr7	90595731	91210589	7q21.13	7q21.13		610679	"CDK14, PFTK1, PFTAIRE1, KIAA0834"	Cyclin-dependent kinase 14	CDK14	5218	ENSG00000058091			Cdk14 (MGI:894318)			
chr7	91264467	91268816	7q21	7q21.13		603408	FZD1	"Frizzled, Drosophila, homolog of, 1"	FZD1	8321	ENSG00000157240			Fzd1 (MGI:1196625)			
chr7	91500000	98400000	7q21.2-q21.3			183600	"SHFM1, SHFD1, SHSF1"	Split hand/foot malformation (ectrodactyly) type 1				contiguous gene deletion syndrome	"Split hand/foot malformation 1, 183600 (4), Autosomal dominant"				
chr7	91872875	91880732	7q21.2	7q21.2		602318	MTERF	"Transcription termination factor, mitochondrial"	MTERF1	7978	ENSG00000127989			"Mterf1a,Mterf1b (MGI:1918240,MGI:3704243)"			
chr7	91940866	92112907	7q21-q22	7q21.2		604001	"AKAP9, YOTIAO, AKAP450"	A-kinase anchor protein 9	AKAP9	10142	ENSG00000127914	mutation identified in 1 LQT11 family	"?Long QT syndrome-11, 611820 (3), Autosomal dominant"				
chr7	92112148	92134744	7q21.2-q21.3	7q21.2		601637	"CYP51A1, CYP51"	"Cytochrome P450, family 51, subfamily A, polypeptide 1 (lanosterol 14-alpha-demethylase)"	CYP51A1	1595	ENSG00000001630			Cyp51 (MGI:106040)			
chr7	92198968	92246099	7q11.2-q21	7q21.2		604214	"CCM1, CAM, KRIT1"	KREV interaction trapped 1	KRIT1	889	ENSG00000001631		"Cavernous malformations of CNS and retina, 116860 (3), Autosomal dominant; Cerebral cavernous malformations-1, 116860 (3), Autosomal dominant; Hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations, 116860 (3), Autosomal dominant"	Krit1 (MGI:1930618)			
chr7	92447447	92494630	7q21.2	7q21.2		614518	"GATAD1, ODAG, CMD2B"	GATA zinc finger domain-containing protein 1	GATAD1	57798	ENSG00000157259	mutation identified in 1 GATAD1 family	"?Cardiomyopathy, dilated, 2B, 614672 (3), Autosomal recessive"	Gatad1 (MGI:1914460)			
chr7	92468379	92477914	7q21-q22	7q21.2		604659	"ERVW1, ERVWE1, HERVW"	"Endogenous retroviral family W, member 1 (syncytin)"	ERVW-1	30816	ENSG00000242950						
chr7	92487022	92528530	7q21-q22	7q21.2		602136	"PEX1, ZWS1, PBD1A, PBD1B, HMLR1"	Peroxisome biogenesis factor-1	PEX1	5189	ENSG00000127980		"Heimler syndrome 1, 234580 (3), Autosomal recessive; Peroxisome biogenesis disorder 1A (Zellweger), 214100 (3), Autosomal recessive; Peroxisome biogenesis disorder 1B (NALD/IRD), 601539 (3), Autosomal recessive"	Pex1 (MGI:1918632)			
chr7	92604920	92836626	7q21-q22	7q21.2		603368	"CDK6, PLSTIRE, MCPH12"	Cyclin-dependent kinase 6	CDK6	1021	ENSG00000105810	mutation identified in 1 MCPH12 family	"?Microcephaly 12, primary, autosomal recessive, 616080 (3), Autosomal recessive"	Cdk6 (MGI:1277162)			
chr7	93099512	93118022	7q21	7q21.2		610456	"SAMD9, NFTC, MIRAGE"	Sterile alpha motif domain-containing protein 9	SAMD9	54809	ENSG00000205413		"MIRAGE syndrome, 617053 (3), Autosomal dominant; Tumoral calcinosis, familial, normophosphatemic, 610455 (3), Autosomal recessive"				
chr7	93130053	93148398	7q21.2	7q21.2		611170	"SAMD9L, ATXPC"	Sterile alpha motif domain-containing 9-like	SAMD9L	219285	ENSG00000177409		"Ataxia-pancytopenia syndrome, 159550 (3), Autosomal dominant"	Samd9l (MGI:1343184)			
chr7	93188538	93232292	7q21.2-q21.3	7q21.2		614133	"HEPACAM2, MIKI"	Hepacam family member 2	HEPACAM2	253012	ENSG00000188175			Hepacam2 (MGI:2141520)			
chr7	93232339	93361122	7q21.2-q21.3	7q21.2-q21.3		616465	"VPS50, CCDC132, KIAA1861"	"VPS50, EARP/GARPII complex subunit"	VPS50	55610	ENSG00000004766			Vps50 (MGI:1920538)			
chr7	93424486	93574729	7q21.3	7q21.3		114131	"CALCR, CRT"	Calcitonin receptor	CALCR	799	ENSG00000004948	not deleted in Williams syndrome	"{Osteoporosis, postmenopausal, susceptibility}, 166710 (3), Autosomal dominant"	Calcr (MGI:101950)			
chr7	93483935	93484018	7q21.3	7q21.3		614523	MIR489	Micro RNA 489	MIR489	574442		in intron 4 of CALCR					
chr7	93885396	93890990	7q22	7q21.3		600033	TFPI2	Tissue factor pathway inhibitor-2	TFPI2	7980	ENSG00000105825			Tfpi2 (MGI:108543)			
chr7	93906507	93911264	7q21.3	7q21.3		189970	GNGT1	"Guanine nucleotide-binding protein, gamma-transducing activity polypeptide 1"	GNGT1	2792	ENSG00000127928			Gngt1 (MGI:109165)			
chr7	93921703	93926513	7q21.3	7q21.3		604390	GNG11	"Guanine nucleotide-binding protein, gamma 11"	GNG11	2791	ENSG00000127920			Gng11 (MGI:1913316)			
chr7	93962769	94004381	7q21.3	7q21.3		605456	BET1	Bet1 golgi vesicular membrane-trafficking protein	BET1	10282	ENSG00000105829			Bet1 (MGI:1343104)			
chr7	94394560	94431231	7q22.1	7q21.3		120160	"COL1A2, EDSCV, EDSARTH2"	"Collagen I, alpha-2 polypeptide"	COL1A2	1278	ENSG00000164692	~17cM from CF	"Ehlers-Danlos syndrome, arthrochalasia type, 2, 617821 (3); Ehlers-Danlos syndrome, cardiac valvular type, 225320 (3), Autosomal recessive; imperfecta, type III, 259420 (3), Autosomal dominant; Osteogenesis imperfecta, type II, 166210 (3), Autosomal dominant; Osteogenesis imperfecta, type IV, 166220 (3), Autosomal dominant; {Osteoporosis, postmenopausal}, 166710 (3), Autosomal dominant"	Col1a2 (MGI:88468)			
chr7	94509857	94633464	7q21	7q21.3		611686	"CASD1, C7orf12"	CAS1 domain-containing protein 1	CASD1	64921	ENSG00000127995			Casd1 (MGI:2384865)			
chr7	94585223	94656208	7q21	7q21.3		604149	"SGCE, DYT11"	"Sarcoglycan, epsilon"	SGCE	8910	ENSG00000127990	pseudogene on 2q21; maternally imprinted	"Dystonia-11, myoclonic, 159900 (3), Autosomal dominant"	Sgce (MGI:1329042)			
chr7	94656324	94669694	7q21	7q21.3		609810	"PEG10, KIAA1051"	Paternally expressed gene 10	PEG10	23089	ENSG00000242265			Peg10 (MGI:2157785)			
chr7	94907201	95296414	7q21.3	7q21.3		602468	"PPP1R9A, NRBI, NRB1, KIAA1222"	"Protein phosphatase 1, regulatory subunit 9A (neurabin I)"	PPP1R9A	55607	ENSG00000158528			Ppp1r9a (MGI:2442401)			
chr7	95297675	95324705	7q21.3	7q21.3		168820	"PON1, PON, ESA, MVCD5"	Paraoxonase-1	PON1	5444	ENSG00000005421		"{Coronary artery disease, susceptibility to} (3); {Coronary artery spasm 2, susceptibility to (3); {Microvascular complications of diabetes 5}, 612633 (3); {Organophosphate poisoning, sensitivity to} (3)"	Pon1 (MGI:103295)			
chr7	95359871	95396374	7q21.3	7q21.3		602720	PON3	Paraoxonase-3	PON3	5446	ENSG00000105852			Pon3 (MGI:106686)			
chr7	95404861	95435071	7q21.3	7q21.3		602447	PON2	Paraoxonase-2	PON2	5445	ENSG00000105854		"{Coronary artery disease, susceptibility to} (3)"	Pon2 (MGI:106687)			
chr7	95485438	95544737	7q21-q22	7q21.3		605761	ASB4	Ankyrin repeat-containing SOCS box protein 4	ASB4	51666	ENSG00000005981			Asb4 (MGI:1929751)			
chr7	95583496	95596612	7q21.3-q22.1	7q21.3		602527	PDK4	"Pyruvate dehydrogenase kinase, isoenzyme 4"	PDK4	5166	ENSG00000004799			Pdk4 (MGI:1351481)			
chr7	95772505	96110321	7q21.3-q22.1	7q21.3		603772	DNCI1	"Dynein, cytoplasmic, intermediate chain 1"	DYNC1I1	1780	ENSG00000158560			Dync1i1 (MGI:107743)			
chr7	96120219	96322146	7q21.3	7q21.3		603859	"SLC25A13, CTLN2"	"Solute carrier family 25 (mitochondrial carrier, citrin), member 13"	SLC25A13	10165	ENSG00000004864		"Citrullinemia, adult-onset type II, 603471 (3), Autosomal recessive; Citrullinemia, type II, neonatal-onset, 605814 (3), Autosomal recessive"	Slc25a13 (MGI:1354721)			
chr7	96481625	96709890	7q21.3-q22.1	7q21.3		601285	"SEM!, DSS1"	Proteasome 26S subunit SEM1	SEM1	7979	ENSG00000127922	?gene mutant in SHFM1		Sem1 (MGI:109238)			
chr7	97005977	97011039	7q22	7q21.3		600030	DLX6	Distal-less homeo box-6	DLX6	1750	ENSG00000006377			Dlx6 (MGI:101927)			
chr7	97020389	97024830	7q22	7q21.3		600028	"DLX5, SHFM1D"	Distal-less homeo box-5	DLX5	1749	ENSG00000105880	mutation identified in 1 family	"?Split-hand/foot malformation 1 with sensorineural hearing loss, 220600 (3), Autosomal recessive"	Dlx5 (MGI:101926)			
chr7	97116592	97181762	7q21.3	7q21.3		615773	ACN9	"Acn9, S. cerevisiae, homolog of"	SDHAF3	57001	ENSG00000196636			Sdhaf3 (MGI:1913288)			
chr7	97731958	97740471	7q21-q22	7q21.3		162320	"TAC1, TAC2, NKNA"	Tachykinin 1 (substance K; neurokinin A; neurokinin 2; neuromedin L; neuropeptide gamma; tachykinin 2)	TAC1	6863	ENSG00000006128			Tac1 (MGI:98474)			
chr7	97852116	97928561	7q21-q31	7q21.3		108370	"ASNS, ASNSD"	Asparagine synthetase	ASNS	440	ENSG00000070669	temperature sensitive G1 mutant	"Asparagine synthetase deficiency, 615574 (3), Autosomal recessive"	Asns (MGI:1350929)			
chr7	98106867	98209635	7q21.3-q22.1	7q21.3		610989	"LMTK2, KPI2, BREK, KIAA1079"	Lemur tyrosine kinase 2	LMTK2	22853	ENSG00000164715			Lmtk2 (MGI:3036247)			
chr7	98212253	98212958	7q21	7q21.3		608606	"BHLHA15, MIST1"	"Basic helix-loop-helix family, member A15"	BHLHA15	168620	ENSG00000180535			Bhlha15 (MGI:891976)			
chr7	98215442	98252250	7q21.3	7q21.3		614781	"TECPR1, KIAA1358"	Tectonin beta-propeller repeat-containing 1	TECPR1	25851	ENSG00000205356			Tecpr1 (MGI:1917631)			
chr7	98281666	98322397	7q21.3	7q21.3		615628	BRI3	Brain protein I3	BRI3	25798	ENSG00000164713			Bri3 (MGI:1933174)			
chr7	98291649	98401114	7q21.3-q22.1	7q21.3-q22.1		611877	"BAIAP2L1, IRTKS"	BAI1-associated protein 2-like 1	BAIAP2L1	55971	ENSG00000006453			Baiap2l1 (MGI:1914148)			
chr7	98400000	107800000	7q22			209850	AUTS1	"Autism, susceptibility to, 1"		100188832			"{Autism susceptibility 1}, 209850 (2), Isolated cases, Multifactorial"				
chr7	98400000	132900000	7q22-q32			148750	G7P1	Kinase-like protein									
chr7	98400000	104200000	7q22.1			612130	GAEC1	Gene amplified in esophageal cancer 1		100126794							
chr7	98400000	107800000	7q22			191390	IBD11	Inflammatory bowel disease 11		100529151		associated with MUC3A	"{Inflammatory bowel disease 11}, 191390 (2), Multifactorial"				
chr7	98400000	107800000	7q22			605633	MUC3B	"Mucin 3B, intestinal"	MUC3B	57876							
chr7	98400000	107800000	7q22			608580	MYH16	"Myosin, heavy chain 16, skeletal muscle"	MYH16	84176		inactivated in humans; expressed in masticatory muscles in nonhuman primates					
chr7	98400000	159345973	7q22-qter			162820	"NM, NCR"	"Neutrophil migration, abnormal"	NM	4827			"?Neutrophil chemotactic response, abnormal, 162820 (2), Autosomal dominant"				
chr7	98400000	107800000	7q22			608562	PAPA4	"Polydactyly, postaxial, type A4"		450096		highest lod with D7S1799	"Polydactyly, postaxial, type A4, 608562 (2)"				
chr7	98400000	132900000	7q22-q32			607458	"SCA18, SMNA"	Spinal cerebellar ataxia 18	SCA18	94008		between D7S2418 and D7S1804	"Spinocerebellar ataxia 18, 607458 (2), Autosomal dominant"				
chr7	98617284	98629868	7q21.3-q22.1	7q22.1		600750	NPTX2	Pentraxin II	NPTX2	4885	ENSG00000106236			Nptx2 (MGI:1858209)			
chr7	98878489	99013242	7q21.2-q22.1	7q22.1		603015	TRRAP	Transformation/transcription domain-associated protein	TRRAP	8295	ENSG00000196367			Trrap (MGI:2153272)			
chr7	99027434	99144119	7q21.1-q31.1	7q22.1		605568	SMURF1	SMAD ubiquitination regulatory factor 1	SMURF1	57154	ENSG00000198742			Smurf1 (MGI:1923038)			
chr7	99145466	99219416	7q22.1	7q22.1		614107	KPNA7	Karyopherin alpha 7	KPNA7	402569	ENSG00000185467			Kpna7 (MGI:2141165)			
chr7	99325872	99366261	7q21-q22	7q22.1		604220	"ARPC1A, SOP2L"	"Actin-related protein 2/3 complex, subunit 1A"	ARPC1A	10552	ENSG00000241685			Arpc1a (MGI:1928896)			
chr7	99374253	99394804	7q21-q22	7q22.1		604223	"ARPC1B, ARC41, PLTEID"	"Actin-related protein 2/3 complex, subunit 1B"	ARPC1B	10095	ENSG00000130429		"Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, 617718 (3), Autosomal recessive"	Arpc1b (MGI:1343142)			
chr7	99394672	99408681	7q22.1	7q22.1		607075	"PDAP1, PAP1, PAP"	PDGFA-associated protein 1	PDAP1	11333	ENSG00000106244			Pdap1 (MGI:2448536)			
chr7	99408619	99419615	7q22.1	7q22.1		603477	"BUD31, G10"	"Bud31, S. cerevisiae, homolog of"	BUD31	8896	ENSG00000106245						
chr7	99416738	99438838	7q22.1	7q22.1		614774	"PTCD1, KIAA0632"	Pentatricopeptide repeat domain 1	PTCD1	26024	ENSG00000106246						
chr7	99438911	99457376	7q21-q22	7q22.1		603052	"CPSF4, CPSF30, NEB1"	"Cleavage-polyadenylation specificity factor 4, 30kD"	CPSF4	10898	ENSG00000160917			Cpsf4 (MGI:1861602)			
chr7	99504643	99534105	7q22.1	7q22.1		611272	"ZKSCAN5, ZFP95, KIAA1015"	Zinc finger protein with KRAB and SCAN domains 5	ZKSCAN5	23660	ENSG00000196652			Zkscan5 (MGI:107533)			
chr7	99558421	99576452	7q22.1	7q22.1		617891	"ZNF655, VIK"	Zinc finger protein 655	ZNF655	79027	ENSG00000197343			Zfp655 (MGI:1919861)			
chr7	99648188	99680025	7q22.1	7q22.1		605325	"CYP3A5, P450PCN3"	"Cytochrome P450, subfamily IIIA, polypeptide 5"	CYP3A5	1577	ENSG00000106258		"{Hypertension, salt-sensitive essential, susceptibility to}, 145500 (3), Multifactorial"	"Cyp3a16,Cyp3a11,Cyp3a41b,Cyp3a44,Cyp3a41a (MGI:2449818,MGI:106099,MGI:3714859,MGI:88609,MGI:1858451)"			
chr7	99705036	99735199	7q22.1	7q22.1		605340	CYP3A7	"Cytochrome P450, subfamily IIIA, polypeptide 7"	CYP3A7	1551	ENSG00000160870			Cyp3a13 (MGI:88610)			
chr7	99756959	99784187	7q22.1	7q22.1		124010	CYP3A4	"Cytochrome P450, subfamily IIIA (nifedipine oxidase) polypeptide 4"	CYP3A4	1576	ENSG00000160868						
chr7	99827625	99867137	7q22.1	7q22.1		606534	CYP3A43	"Cytochrome P450, subfamily IIIa, polypeptide 43"	CYP3A43	64816	ENSG00000021461						
chr7	99923268	99929619	7q22.1	7q22.1		611925	"GJC3, CX30.2, CX31.3"	"Gap junction protein, gamma-3"	GJC3	349149	ENSG00000176402			Gjc3 (MGI:2153041)			
chr7	99966726	99976111	7q22.1	7q22.1		194460	"AZGP1, ZAG"	"Alpha-2-glycoprotein, zinc"	AZGP1	563	ENSG00000160862			Azgp1 (MGI:103163)			
chr7	100015551	100045373	7q21-q22	7q22.1		601260	"ZNF36, KOX18"	Zinc finger protein-36 (KOX 18)	ZKSCAN1	7586	ENSG00000106261			Zkscan1 (MGI:1921820)			
chr7	100049773	100065040	7q21-q22	7q22.1		601261	"ZNF38, KOX25"	Zinc finger protein-38 (KOX 25)	ZSCAN21	7589	ENSG00000166529			Zscan21 (MGI:99182)			
chr7	100063846	100082547	7q22.1	7q22.1		194510	ZNF3	Zinc finger protein-3	ZNF3	7551	ENSG00000166526	"?relation to ZNF4, ZNF5; previous assignment to Chr.5"		Zfp113 (MGI:1929116)			
chr7	100088959	100092199	7q22.1	7q22.1		614729	"COPS6, CSN6"	"COP9 signalosome, subunit 6"	COPS6	10980	ENSG00000168090			Cops6 (MGI:1349439)			
chr7	100092727	100101939	7q21.3-q22.1	7q22.1		600592	"MCM7, MCM2"	"Minichromosome maintenance deficient, S. cerevisiae, homolog of, 7"	MCM7	4176	ENSG00000166508			Mcm7 (MGI:1298398)			
chr7	100093559	100093642	7q22.1	7q22.1		612150	"MIR25, MIRN25"	Micro RNA 25	MIR25	407014							
chr7	100093767	100093846	7q22	7q22.1		612984	"MIR93, MIRN9"	Micro RNA 93	MIR93	407050							
chr7	100093992	100094073	7q22	7q22.1		612983	"MIR106B, MIRN106B"	Micro RNA 106B	MIR106B	406900							
chr7	100101412	100107179	7q22.1	7q22.1		602296	"AP4M1, SPG50, CPSQ3"	"Adaptor-related protein complex 4, mu-1 subunit"	AP4M1	9179	ENSG00000221838		"Spastic paraplegia 50, autosomal recessive, 612936 (3), Autosomal recessive"	Ap4m1 (MGI:1337063)			
chr7	100107069	100127207	7q22.1	7q22.1		602955	"TAF6, TAF2E, TAFII80, ALYUS"	"TAF6 RNA polymerase II, TATA box-binding protein-associated factor, 80kD"	TAF6	6878	ENSG00000106290		"Alazami-Yuan syndrome, 617126 (3), Autosomal recessive"	Taf6 (MGI:109129)			
chr7	100119641	100125507	7q22.1	7q22.1		610047	"CNPY4, PRAT4B, MGC40499"	"Canopy 4, zebrafish, homolog of"	CNPY4	245812	ENSG00000166997			Cnpy4 (MGI:1913705)			
chr7	100159241	100168749	7q22	7q22.1		608235	GAL3ST4	Galactose-3-O-sulfotransferase 4	GAL3ST4	79690	ENSG00000197093			Gal3st4 (MGI:1916254)			
chr7	100177562	100219333	7q22	7q22.1		608489	"STAG3, POF8"	Stromalin 3	STAG3	10734	ENSG00000066923		"Premature ovarian failure 8, 615723 (3), Autosomal recessive"	Stag3 (MGI:1355311)			
chr7	100218624	100221488	7q22.1	7q22.1		617012	"PVRIG, CD112R, C7orf15"	Poliovirus receptor-related immunoglobulin domain-containing protein	PVRIG	79037	ENSG00000213413			Pvrig (MGI:5596028)			
chr7	100306797	100322195	7q22.1	7q22.1		617625	"SPDYE3, SPDYB2"	"SPEEDY/RINGO cell cycle regulator family, member E3"	SPDYE3	441272	ENSG00000214300						
chr7	100320639	100336306	7q22.1	7q22.1		605038	"PMS2P1, PMS2L1, PMS3"	Postmeiotic segregation increased 2 pseudogene 1	PMS2P1	5379							
chr7	100358002	100367830	7q22	7q22.1		605342	PILRB	"Paired immunoglobulin-like receptor, beta"	PILRB	29990	ENSG00000121716			"Pilrb1,Pilrb2 (MGI:2450532,MGI:2450535)"			
chr7	100372658	100400098	7q22	7q22.1		605341	PILRA	"Paired immunoglobulin-like receptor, alpha"	PILRA	29992	ENSG00000085514			Pilra (MGI:2450529)			
chr7	100428789	100434125	7q22	7q22.1		611478	"MEPCE, BCDIN3"	Methylphosphate capping enzyme	MEPCE	56257	ENSG00000146834			Mepce (MGI:106477)			
chr7	100466518	100479278	7p21-p15	7q22.1		611914	"TSC22D4, THG1"	"TSC22 domain family, member 4"	TSC22D4	81628	ENSG00000166925			Tsc22d4 (MGI:1926079)			
chr7	100483926	100494801	7q22.1	7q22.1		615477	NYPA1	Neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1	NYAP1	222950	ENSG00000166924			Nyap1 (MGI:2443880)			
chr7	100539210	100568219	7q22.1	7q22.1		604019	"AGFG2, HRBL, RABR"	ADP-ribosylation factor GTPase-activating protein with FG repeats 2	AGFG2	3268	ENSG00000106351			Agfg2 (MGI:2443267)			
chr7	100574034	100574732	7q22	7q22.1		617677	ZASP	ZO2-associated speckle protein		101927655							
chr7	100582489	100601116	7q22	7q22.1		609097	"FBXO24, FBX24"	F-box only protein 24	FBXO24	26261	ENSG00000106336			Fbxo24 (MGI:1918426)			
chr7	100602258	100608174	7q21.3-q22	7q22.1		600270	PCOLCE	Procollagen C-endopeptidase enhancer	PCOLCE	5118	ENSG00000106333			Pcolce (MGI:105099)			
chr7	100620415	100642779	7q22	7q22.1		604720	"TFR2, HFE3"	Transferrin receptor 2	TFR2	7036	ENSG00000106327		"Hemochromatosis, type 3, 604250 (3), Autosomal recessive"	Tfr2 (MGI:1354956)			
chr7	100643096	100656460	7q22	7q22.1		612458	"ACTL6B, BAF53B"	Actin-like 6B	ACTL6B	51412	ENSG00000077080			Actl6b (MGI:1933548)			
chr7	100673739	100679168	7q21	7q22.1		139390	GNB2	"Guanine nucleotide-binding protein, beta polypeptide-2"	GNB2	2783	ENSG00000172354	30-70kb from EPO		Gnb2 (MGI:95784)			
chr7	100679505	100694279	7q22.1	7q22.1		612064	GIGYF1	GRB10-interacting GYF protein 1	GIGYF1	64599	ENSG00000146830			Gigyf1 (MGI:1888677)			
chr7	100706052	100707499	7q22	7q22.1		606113	"POP7, RPP20"	"Processing of precursor 7, S. cerevisiae, homolog of"	POP7	10248	ENSG00000172336			Pop7 (MGI:1921347)			
chr7	100720799	100723699	7q21	7q22.1		133170	"EPO, MVCD2, ECYT5, DBAL"	Erythropoietin	EPO	2056	ENSG00000130427	mutation identified in 1 DBAL family	"?Diamond-Blackfan anemia-like, 617911 (3); Erythrocytosis, familial, 5, 617907 (3), Autosomal dominant; {Microvascular complications of diabetes 2}, 612623 (3)"	Epo (MGI:95407)			
chr7	100733598	100797796	7q22	7q22.1		602372	ZAN	Zonadhesin	ZAN	7455	ENSG00000146839			Zan (MGI:106656)			
chr7	100802564	100827520	7q22	7q22.1		600011	"EPHB4, HTK, MYK1, HFASD"	Ephrin receptor EphB4 (hepatoma transmembrane kinase)	EPHB4	2050	ENSG00000196411		"{Hydrops fetalis, nonimmune, and/or atrial septal defect}, 617300 (3), Autosomal dominant"	Ephb4 (MGI:104757)			
chr7	100826873	100867011	7q22	7q22.1		616861	"SLC12A9, CIP1, CCC6"	"Solute carrier family 12 (potassium/chloride transporter), member 9"	SLC12A9	56996	ENSG00000146828			Slc12a9 (MGI:1933532)			
chr7	100867327	100873453	7q22	7q22.1		602933	"TRIP6, OIP1"	Thyroid hormone receptor interactor-6	TRIP6	7205	ENSG00000087077			Trip6 (MGI:1343458)			
chr7	100874970	100888663	7q22	7q22.1		614469	"SRRT, ARS2"	"Serrate RNA effector molecule, arabidopsis, homolog of"	SRRT	51593	ENSG00000087087			Srrt (MGI:1933527)			
chr7	100888722	100889717	7q22.1	7q22.1		611481	UFSP1	UFM1-specific protease 1	UFSP1	402682	ENSG00000176125			Ufsp1 (MGI:1917490)			
chr7	100889993	100896132	7q22	7q22.1		100740	"ACHE, YT"	Acetylcholinesterase (YT blood group)	ACHE	43	ENSG00000087085	blood group YT (112100) = epitope of ACHE	"[Blood group, Yt system], 112100 (3)"	Ache (MGI:87876)			
chr7	100949053	100968346	7q22	7q22.1		158371	MUC3A	"Mucin 3A, intestinal"	MUC3A	4584	ENSG00000169894			Muc3a (MGI:3588263)			
chr7	100969622	101018948	7q22	7q22.1		604609	"MUC12, MUC11"	Mucin 12	MUC12	10071	ENSG00000205277						
chr7	101020082	101058858	7q22	7q22.1		608424	MUC17	Mucin 17	MUC17	140453	ENSG00000169876						
chr7	101085423	101091741	7q22.1	7q22.1		616996	TRIM56	Tripartite motif-containing protein 56	TRIM56	81844	ENSG00000169871			Trim56 (MGI:2685298)			
chr7	101127088	101139265	7q21.3-q22	7q22.1		173360	"PAI1, PLANH1, SERPINE1"	"Plasminogen activator inhibitor, type I"	SERPINE1	5054	ENSG00000106366		"Plasminogen activator inhibitor-1 deficiency, 613329 (3), Autosomal recessive, Autosomal dominant; {Transcription of plasminogen activator inhibitor, modulator of} (3)"	Serpine1 (MGI:97608)			
chr7	101154397	101161276	7q22.1	7q22.1		603531	"AP1S1, CLAPS1, AP19, MEDNIK"	"Adaptor-related protein complex 1, sigma 1 subunit"	AP1S1	1174	ENSG00000106367		"MEDNIK syndrome, 609313 (3), Autosomal recessive"	Ap1s1 (MGI:1098244)			
chr7	101162508	101169955	7q22	7q22.1		602186	VGF	VGF nerve growth factor inducible	VGF	7425	ENSG00000128564			Vgf (MGI:1343180)			
chr7	101170492	101180275	7q22.1	7q22.1		615783	NAT16	N-acetyltransferase 16	NAT16	375607	ENSG00000167011						
chr7	101192885	101201130	7q22.1	7q22.1		610184	"MOGAT3, MGAT3"	Monoacylglycerol O-acyltransferase 3	MOGAT3	346606	ENSG00000106384						
chr7	101205976	101217729	7q22	7q22.1		603066	"PLOD3, LH3"	"Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 (lysyl hydroxylase 3)"	PLOD3	8985	ENSG00000106397	previously assigned to 7q36	"Lysyl hydroxylase 3 deficiency, 612394 (3), Autosomal recessive"	Plod3 (MGI:1347008)			
chr7	101232091	101238819	7q22.1	7q22.1		615778	CLDN15	Claudin 15	CLDN15	24146	ENSG00000106404			Cldn15 (MGI:1913103)			
chr7	101239611	101245089	7q22.1	7q22.1		609003	"TTC11, FIS1"	Tetratricopeptide repeat domain 11	FIS1	51024	ENSG00000214253			Fis1 (MGI:1913687)			
chr7	101613324	101629295	7q22.1	7q22.1		617177	"MYL10, PLRLC"	Myosin light chain 10	MYL10	93408	ENSG00000106436			Myl10 (MGI:1891705)			
chr7	101815903	102283957	7q22	7q22.1		116896	"CUTL1, CDP"	"Cut, Drosophila, homolog of (CCAAT displacement protein)"	CUX1	1523	ENSG00000257923						
chr7	102284524	102321710	7q22	7q22.1		605300	APS	Adaptor protein containing PH and SH2 domains	SH2B2	10603	ENSG00000160999			Sh2b2 (MGI:1345171)			
chr7	102396356	102426681	7q22.1	7q22.1		617458	"PRKRIP1, C114"	"PRKR-interacting protein 1, IL11-inducible"	PRKRIP1	79706	ENSG00000128563			Prkrip1 (MGI:1914051)			
chr7	102433529	102456820	7q22.1	7q22.1		610929	"ORAI2, MEM142B, C7orf19"	ORAI calcium release-activated calcium modulator 2	ORAI2	80228	ENSG00000160991			Orai2 (MGI:2443195)			
chr7	102456219	102464873	7q22.1	7q22.1		613302	"ALKBH4, ABH4"	"AlkB, E. coli, homolog of, 4"	ALKBH4	54784	ENSG00000160993			Alkbh4 (MGI:1919291)			
chr7	102464882	102473167	7q22.1	7q22.1		615167	"LRWD1, ORCA"	Leucine-rich repeats- and WD repeat domain-containing protein 1	LRWD1	222229	ENSG00000161036			Lrwd1 (MGI:1918985)			
chr7	102473099	102478933	7q22-q31.1	7q22.1		604150	POLR2J	"Polymerase II, RNA, subunit J"	POLR2J	5439	ENSG00000005075			Polr2j (MGI:109582)			
chr7	102579645	102616757	7q22	7q22.1		607943	"RASA4, CAPRI, GAPL, KIAA0538"	Ras p21 protein activator 4	RASA4	10156	ENSG00000105808			Rasa4 (MGI:1858600)			
chr7	102636747	102671728	7q11.2	7q22.1		609881	"POLR2J2, RPB11"	RNA polymerase II polypeptide J-related gene	POLR2J2	246721	ENSG00000228049						
chr7	102810965	103075215	7q22.1	7q22.1		609080	"EBXL13, FBL13"	F-box and leucine-rich repeat protein 13	FBXL13	222235	ENSG00000161040			Fbxl13 (MGI:2443416)			
chr7	102973436	102978666	7q22.1	7q22.1		612133	NFE4	Transcription factor NFE4	NFE4	58160	ENSG00000230257						
chr7	103074880	103099772	7q11.2	7q22.1		611864	"ARMC10, SVH"	Armadillo repeat-containing 10	ARMC10	83787	ENSG00000170632			Armc10 (MGI:1914461)			
chr7	103099575	103149559	7q22.1	7q22.1		612334	NAPEPLD	N-acyl phosphatidylethanolamine-hydrolyzing phospholipase D	NAPEPLD	222236	ENSG00000161048			Napepld (MGI:2140885)			
chr7	103297425	103329901	7q22-q31.1	7q22.1		603131	MPPB	Mitochondrial processing peptidase-beta	PMPCB	9512	ENSG00000105819			Pmpcb (MGI:1920328)			
chr7	103312473	103344872	7q22	7q22.1		605502	"DNAJC2, ZRF1, MPP11"	"DnaJ (Hsp40) homolog, subfamily C, member 2"	DNAJC2	27000	ENSG00000105821			Dnajc2 (MGI:99470)			
chr7	103344404	103369394	7q22.1-q22.3	7q22.1		154365	"PSMC2, MSS1, S7"	"Proteasome 26S subunit, ATPase, 2"	PSMC2	5701	ENSG00000161057			Psmc2 (MGI:109555)			
chr7	103352597	103446176	7q22.1	7q22.1		604943	"SLC26A5, PRES, DFNB61"	"Solute carrier family 26, member 5"	SLC26A5	375611	ENSG00000170615	mutation identified in 1 DFNB61 family	"?Deafness, autosomal recessive 61, 613865 (3), Autosomal recessive"	Slc26a5 (MGI:1933154)			
chr7	103471783	103989515	7q22	7q22.1		600514	"RELN, RL, LIS2, ETL7"	Reelin	RELN	5649	ENSG00000189056		"{Epilepsy, familial temporal lobe, 7}, 616436 (3), Autosomal dominant; Lissencephaly 2 (Norman-Roberts type), 257320 (3), Autosomal recessive"	Reln (MGI:103022)			
chr7	104126340	104208046	7q22.1	7q22.1-q22.2		602331	"ORC5, ORC5L"	"Origin recognition complex, subunit 5, S. cerevisiae, homolog of"	ORC5	5001	ENSG00000164815			Orc5 (MGI:1347044)			
chr7	104328655	104908557	7q22.1	7q22.2-q22.3		609719	LHFPL3	LHFP-like protein 3	LHFPL3	375612				Lhfpl3 (MGI:1925076)			
chr7	104900000	115000000	7q22.3-q31.1			609915	CMD1Q	"Cardiomyopathy, dilated, 1Q"	CMD1Q	664728		between D7S2545 and D7S2554	"Cardiomyopathy, dilated, 1Q, 609915 (2)"				
chr7	104900000	107800000	7q22.3			614646	MPVQTL6	Mean platelet volume quantitative trait locus 6		100887751		associated with rs342293	"Mean platelet volume QTL6, 614646 (2)"				
chr7	104940948	105114084	7q22	7q22.3		608444	"KMT2E, MLL5"	Lysine (K)-specific methyltransferase 2E	KMT2E	55904	ENSG00000005483			Kmt2e (MGI:1924825)			
chr7	105456500	105522257	7q22.3	7q22.3		616261	"PUS7, KIAA1897"	"Pseudouridylate synthase 7, putative"	PUS7	54517	ENSG00000091127			Pus7 (MGI:1925947)			
chr7	105532080	105567683	7q22.3	7q22.3		610089	RINT1	RAD50-interacting protein 1	RINT1	60561	ENSG00000135249			Rint1 (MGI:1916233)			
chr7	105876749	106036430	7q22.3	7q22.3		615610	CDHR3	"Cadherin-related family, member 3"	CDHR3	222256	ENSG00000128536			Cdhr3 (MGI:1916014)			
chr7	106090367	106112646	7q22.3	7q22.3		616665	"SYPL1, SYPL"	Synaptophysin-like 1	SYPL1	6856	ENSG00000008282			Sypl (MGI:108081)			
chr7	106248284	106285191	7q22.2	7q22.3		608764	"NAMPT, PBEF1, VF, PBEF"	Nicotinamide phosphoribosyltransferase	NAMPT	10135	ENSG00000105835			Nampt (MGI:1929865)			
chr7	106865277	106908977	7q22	7q22.3		601232	PIK3CG	"Phosphatidylinositol 3-kinase, catalytic, gamma"	PIK3CG	5294	ENSG00000105851			Pik3cg (MGI:1353576)			
chr7	107044727	107161810	7q22	7q22.3		176912	PRKAR2B	"Protein kinase, cAMP-dependent, regulatory, type II, beta"	PRKAR2B	5577	ENSG00000005249			Prkar2b (MGI:97760)			
chr7	107168960	107202528	7q22.3	7q22.3		616714	HBP1	HMG-box transcription factor 1	HBP1	26959	ENSG00000105856			Hbp1 (MGI:894659)			
chr7	107201743	107564513	7q31	7q22.3		606821	"COG5, GOLTC1, GTC90, CDG2I"	Component of oligomeric golgi complex 5	COG5	10466	ENSG00000164597		"Congenital disorder of glycosylation, type IIi, 613612 (3)"	Cog5 (MGI:2145130)			
chr7	107470056	107476206	7q22-q31.1	7q22.3		601910	GPR22	G protein-coupled receptor-22	GPR22	2845	ENSG00000172209			Gpr22 (MGI:1920260)			
chr7	107660634	107717808	7q31	7q22.3		605646	"SLC26A4, PDS, DFNB4, EVA, TDH2B"	"Solute carrier family 26 (sulfate transporter), member 4"	SLC26A4	5172	ENSG00000091137	some patients have digenic mutations with FOXI1	"Deafness, autosomal recessive 4, with enlarged vestibular aqueduct, 600791 (3), Autosomal recessive; Pendred syndrome, 274600 (3), Autosomal recessive"	Slc26a4 (MGI:1346029)			
chr7	107743696	107764996	7q22.3	7q22.3		606872	"CBLL1, HAKAI, RNF188"	Cas-Br-M murine ectopic retroviral transforming sequence like-1	CBLL1	79872	ENSG00000105879			Cbll1 (MGI:2144842)			
chr7	107765466	107803232	7q22-q31.1	7q22.3-q31.1		126650	"SLC26A3, DRA, CLD"	"Solute carrier family 26 (sulfate transporter), member 3"	SLC26A3	1811	ENSG00000091138	5' and close to PDS	"Diarrhea 1, secretory chloride, congenital, 214700 (3), Autosomal recessive"	Slc26a3 (MGI:107181)			
chr7	107800000	127500000	7q31			611015	AUTS9	"Autism, susceptibility to, 9"				max lod near D7S530	"{Autism, susceptibility to, 9}, 611015 (2)"				
chr7	107800000	127500000	7q31			603678	DFNB14	"Deafness, autosomal recessive 14"	DFNB14	1706		?same as DFNB17	"Deafness, autosomal recessive 14, 603678 (2), Autosomal recessive"				
chr7	107800000	127500000	7q31			603010	DFNB17	"Deafness, autosomal recessive 17"	DFNB17	1709			"Deafness, autosomal recessive 17, 603010 (2), Autosomal recessive"				
chr7	107891106	107921197	7q31-q32	7q31.1		238331	"DLD, LAD, PHE3, DLDD"	"Dihydrolipoamide dehydrogenase (E3 component of pyruvate dehydrogenase complex, 2-oxo-glutarate complex)"	DLD	1738	ENSG00000091140		"Dihydrolipoamide dehydrogenase deficiency, 246900 (3), Autosomal recessive"	Dld (MGI:107450)			
chr7	107923798	108003358	7q31.1-q31.3	7q31.1		150240	"LAMB1, LIS5"	"Laminin, beta-1"	LAMB1	3912	ENSG00000091136		"Lissencephaly 5, 615191 (3), Autosomal recessive"	Lamb1 (MGI:96743)			
chr7	108011661	108130355	7q31.1	7q31.1		616380	LAMB4	"Laminin, beta-4"	LAMB4	22798	ENSG00000091128						
chr7	108147625	108456441	7q31.1-q31.2	7q31.1		601581	NRCAM	Neuronal cell adhesion molecule	NRCAM	4897	ENSG00000091129			Nrcam (MGI:104750)			
chr7	108470421	108528160	7q31	7q31.1		612123	"PNPLA8, MMLA"	Patatin-like phospholipase domain-containing protein 8	PNPLA8	50640	ENSG00000135241	mutation identified in 1 MMLA family	"?Mitochondrial myopathy with lactic acidosis, 251950 (3), Autosomal recessive"	Pnpla8 (MGI:1914702)			
chr7	108562143	108569767	7q31.1	7q31.1		612534	THAP5	THAP domain-containing protein 5	THAP5	168451	ENSG00000177683						
chr7	108569744	108574849	7q31.1	7q31.1		602634	"DNAJB9, MDG1"	"DnaJ, E. coli, homolog of, subfamily B, member 9 (microvascular endothelial differentiation gene-1)"	DNAJB9	4189	ENSG00000128590	previously assigned to chr.14 by FISH		Dnajb9 (MGI:1351618)			
chr7	110662644	111562530	7q31	7q31.1		605977	"IMMP2L, IMP2"	"Inner mitochondrial membrane peptidase, subunit 2, S. cerevisiae, homolog of"	IMMP2L	83943	ENSG00000184903			Immp2l (MGI:2135611)			
chr7	111726107	112206406	7q31	7q31.1		607679	"DOCK4, KIAA0716"	Dedicator of cytokinesis 4	DOCK4	9732	ENSG00000128512			Dock4 (MGI:1918006)			
chr7	112206587	112343933	7q31.1	7q31.1		605465	ZNF277	Zinc finger protein-277	ZNF277	11179	ENSG00000198839			Zfp277 (MGI:1890393)			
chr7	112423143	112477939	7q22-q31	7q31.1		603502	IFRD1	Interferon-related developmental regulator 1	IFRD1	3475	ENSG00000006652			Ifrd1 (MGI:1316717)			
chr7	112819146	112939876	7q31.1	7q31.1		617855	"BMT2, SAMTOR, C7orf60"	"Base methyltransferase of 25S rRNA 2, S. cerevisiae, homolog of"	BMT2	154743	ENSG00000164603			Bmt2 (MGI:2141466)			
chr7	113080412	113087777	7q31	7q31.1		605188	"GPR85, SREB2"	G protein-coupled receptor-85	GPR85	54329	ENSG00000164604			Gpr85 (MGI:1927851)			
chr7	113876826	113919093	7q11.23-q21.11	7q31.1		600917	"PPP1R3A, PPP1R3"	"Protein phosphatase 1, regulatory subunit 3A"	PPP1R3A	5506	ENSG00000154415		"Insulin resistance, severe, digenic, 125853 (3), Autosomal dominant"	Ppp1r3a (MGI:2153588)			
chr7	114086309	114693771	7q31	7q31.1		605317	"FOXP2, SPCH1, TNRC10, CAGH44"	Forkhead box P2	FOXP2	93986	ENSG00000128573		"Speech-language disorder-1, 602081 (3), Autosomal dominant"				
chr7	114922153	115019915	7q31.1	7q31.1-q31.2		614511	"MDFIC, HIC"	MYOD family inhibitor domain-containing protein	MDFIC	29969	ENSG00000135272			Mdfic (MGI:104611)			
chr7	115935147	116159890	7q31.2	7q31.2		604732	"TFEC, TFECL"	Transcription factor EC	TFEC	22797	ENSG00000105967			Tfec (MGI:1333760)			
chr7	116210492	116258785	7q31.2	7q31.2		606085	TES	Testin	TES	26136	ENSG00000135269			Tes (MGI:105081)			
chr7	116499600	116508540	7q31.1	7q31.2		601048	CAV2	Caveolin-2	CAV2	858	ENSG00000105971			Cav2 (MGI:107571)			
chr7	116524784	116561184	7q31.1	7q31.2		601047	"CAV1, BSCL3, CGL3, PPH3, LCCNS"	Caveolin-1	CAV1	857	ENSG00000105974	mutation identified in 1 CGL3 family; mutation identified in 1 LCCNS family	"?Lipodystrophy, congenital generalized, type 3, 612526 (3); ?Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome, 606721 (3), Autosomal dominant; Pulmonary hypertension, primary, 3, 615343 (3), Autosomal dominant"	Cav1 (MGI:102709)			
chr7	116672358	116798385	7q31	7q31.2		164860	"MET, DFNB97, OSFD"	Oncogene MET	MET	4233	ENSG00000105976	mutation identified in 1 DFNB97 family	"?Deafness, autosomal recessive 97, 616705 (3), Autosomal recessive; Hepatocellular carcinoma, childhood type, somatic, 114550 (3); {Osteofibrous dysplasia, susceptibility to}, 607278 (3), Autosomal dominant; Renal cell carcinoma, papillary, 1, familial and somatic, 605074 (3)"	Met (MGI:96969)			
chr7	116862508	116919260	7q31.2-q31.3	7q31.2		601571	"CAPZA2, CAPPA2"	"Capping protein (actin filament) muscle Z-line, alpha 2"	CAPZA2	830	ENSG00000198898			Capza2 (MGI:106222)			
chr7	116953326	117230022	7q31.1	7q31.2		600833	"ST7, TSG7, RAY1, FAM4A1"	Suppressor of tumorigenicity 7 (breast)	ST7	7982	ENSG00000004866			St7 (MGI:1927450)			
chr7	117276630	117323288	7q31	7q31.2		147870	"WNT2, INT1L1"	"Wingless-type MMTV integration site family, member 2"	WNT2	7472	ENSG00000105989	isolated by CMGT with MET		Wnt2 (MGI:98954)			
chr7	117363221	117427522	7q31.3	7q31.2		605797	"ASZ1, ALP1, ANKL1, GASZ"	"Ankyrin repeat, SAM, and basic leucine zipper domain-containing 1"	ASZ1	136991	ENSG00000154438			Asz1 (MGI:1921318)			
chr7	117479962	117668664	7q31.2	7q31.2		602421	"CFTR, ABCC7, CF, MRP7"	"Cystic fibrosis transmembrane conductance regulator (ATP-binding cassette, subfamily C, member 7)"	CFTR	1080	ENSG00000001626	distal and 5' to MET	"{Bronchiectasis with or without elevated sweat chloride 1, modifier of}, 211400 (3), Autosomal dominant; Congenital bilateral absence of vas deferens, 277180 (3), Autosomal recessive; Cystic fibrosis, 219700 (3), Autosomal recessive; {Hypertrypsinemia, neonatal} (3); {Pancreatitis, idiopathic}, 167800 (3), Autosomal dominant; Sweat chloride elevation without CF (3)"	Cftr (MGI:88388)			
chr7	117700000	127500000	7q31.3			606256	STQTL2	Stature quantitative trait locus 2		192143		max lod at D7S195	"{Stature QTL 2}, 606256 (2)"				
chr7	117710647	117873817	7q31	7q31.31		609772	"CTTNBP2, CORTBP2, KIAA1758"	Cortactin-binding protein 2	CTTNBP2	83992	ENSG00000077063			Cttnbp2 (MGI:1353467)			
chr7	118184031	118204038	7q31.31	7q31.31		607288	LSM8	"LSM8, S. cerevisiae, homolog of, U6 small nuclear RNA associated"	LSM8	51691	ENSG00000128534			Lsm8 (MGI:1923772)			
chr7	118224657	118242730	7q31.3	7q31.31		610731	ANKRD7	Ankyrin repeat domain-containing protein 7	ANKRD7	56311	ENSG00000106013			Ankrd7 (MGI:1922446)			
chr7	120273637	120750332	7q31	7q31.31		605410	"KCND2, KIAA1044"	"Potassium voltage-gated channel, Shal-related subfamily, member 2"	KCND2	3751	ENSG00000184408			Kcnd2 (MGI:102663)			
chr7	120787319	120858336	7q31	7q31.31		613138	"TSPAN12, NET2, EVR5"	Tetraspanin 12	TSPAN12	23554	ENSG00000106025		"Exudative vitreoretinopathy 5, 613310 (3), Autosomal dominant"	Tspan12 (MGI:1889818)			
chr7	120950748	120975656	7q31	7q31.31		607493	"ING3, P47ING3"	"Inhibitor of growth family, member 3"	ING3	54556	ENSG00000071243			Ing3 (MGI:1919027)			
chr7	121325366	121341103	7q31.3	7q31.31		606267	WNT16	"Wingless-type MMTV integration site family, member 16"	WNT16	51384	ENSG00000002745			Wnt16 (MGI:2136018)			
chr7	121348850	121396368	7q31.3	7q31.31		608618	FAM3C	"Family with sequence similarity 3, member C"	FAM3C	10447	ENSG00000196937			Fam3c (MGI:107892)			
chr7	121873104	122062035	7q31.3	7q31.32		176891	"PTPRZ1, PTP18"	"Protein-tyrosine phosphatase, receptor-type, zeta-1, polypeptide"	PTPRZ1	5803	ENSG00000106278		"{H. pylori infection, susceptibility to}, 600263 (1)"	Ptprz1 (MGI:97816)			
chr7	122073543	122144289	7q31.3	7q31.32		605113	AASS	Alpha-aminoadipic semialdehyde synthase	AASS	10157	ENSG00000008311		"Hyperlysinemia, 238700 (3), Autosomal recessive; Saccharopinuria, 268700 (1), Autosomal recessive"	Aass (MGI:1353573)			
chr7	122300938	122311854	7q31.32	7q31.32		613301	"FEZF1, FEZ, ZNF312B, HH22"	FEZ family zinc finger protein 1	FEZF1	389549	ENSG00000128610		"Hypogonadotropic hypogonadism 22, with or without anosmia, 616030 (3), Autosomal recessive"	Fezf1 (MGI:1920441)			
chr7	122318423	122886758	7q31.3	7q31.32		609978	"CADPS2, KIAA1591"	Calcium-dependent activator protein for secretion 2	CADPS2	93664	ENSG00000081803			Cadps2 (MGI:2443963)			
chr7	122994704	122995699	7q31	7q31.32		604867	"TAS2R16, T2R16"	"Taste receptor type 2, member 16"	TAS2R16	50833	ENSG00000128519		"{Alcohol dependence, susceptibility to}, 103780 (3), Multifactorial; [Beta-glycopyranoside tasting] (3)"	Tas2r118 (MGI:2681247)			
chr7	123113489	123201835	7q31-q32	7q31.32		606193	"SLC13A1, NAS1"	"Solute carrier family 13 (sodium/sulfate symporters), member 1"	SLC13A1	6561	ENSG00000081800			Slc13a1 (MGI:1859937)			
chr7	123536996	123601650	7q32	7q31.32		601677	"NDUFA5, UQOR13"	"NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 (13kD, B13)"	NDUFA5	4698	ENSG00000128609			Ndufa5 (MGI:1915452)			
chr7	123655806	123664289	7q31.32	7q31.32		608006	"LMOD2, CLMOD"	Leiomodin 2	LMOD2	442721	ENSG00000170807			Lmod2 (MGI:2135672)			
chr7	123681926	123749070	7q31.3	7q31.32		605056	"WASL, NWASP"	Wiskott-Aldrich syndrome gene-like	WASL	8976	ENSG00000106299						
chr7	123763707	123877480	7q31	7q31.32		604510	HYAL4	Hyaluronoglucosaminidase 4	HYAL4	23553	ENSG00000106302			Hyal4 (MGI:1924292)			
chr7	123925231	123971409	7q31	7q31.32		600930	SPAM1	"Sperm adhesion molecule 1 (PH-20 hyaluronidase, zona pellucida binding)"	SPAM1	6677	ENSG00000106304			Hyal5 (MGI:1921718)			
chr7	124743884	124766107	7q31	7q31.33		602583	GPR37	G protein-coupled receptor-37	GPR37	2861	ENSG00000170775			Gpr37 (MGI:1313297)			
chr7	124822385	124929982	7q31.33	7q31.33		606478	"POT1, CMM10, GLM9"	Protection of telomeres 1	POT1	25913	ENSG00000128513		"{Glioma susceptibility 9}, 616568 (3), Autosomal dominant; {Melanoma, cutaneous malignant, susceptibility to, 10}, 615848 (3), Autosomal dominant"	Pot1a (MGI:2141503)			
chr7	126438597	127253292	7q31.3-q32.1	7q31.33		601116	GRM8	"Glutamate receptor, metabotropic-8"	GRM8	2918	ENSG00000179603			Grm8 (MGI:1351345)			
chr7	127500000	132900000	7q32			613063	BCC6	"Basal cell carcinoma, susceptibility to, 6"		100307123		associated with rs157935	"{Basal cell carcinoma, susceptibility to, 6}, 613063 (2)"				
chr7	127500000	132900000	7q32			600676	CATR1	CATR tumorigenic conversion 1	CATR1	856							
chr7	127500000	132900000	7q32			614220	PBC4	"Biliary cirrhosis, primary, 4"		100689215		associated with rs10488631	"Biliary cirrhosis, primary, 4, 614220 (2)"				
chr7	127500000	132900000	7q32			609573	PPR3	Photoparoxysmal response 3		619471		max lod at D7S1804	"Photoparoxysmal response 3, 609573 (2)"				
chr7	127500000	138500000	7q32-q33			613909	SCA32	Spinocerebellar ataxia 32	SCA32	100653368		between rs3847110 and rs2241728	"Spinocerebellar ataxia 32, 613909 (2), Autosomal dominant"				
chr7	127580627	127585599	7q32.1	7q32.1		607418	"GCC1, GCC88"	GRIP and coiled-coil domains-containing protein 1	GCC1	79571	ENSG00000179562			Gcc1 (MGI:1921625)			
chr7	127588351	127591704	7q31.3	7q32.1		103188	ARF5	ADP-ribosylation factor 5	ARF5	381	ENSG00000004059			Arf5 (MGI:99434)			
chr7	127593634	127601796	7q31.3	7q32.1		615800	FSCN3	"Fascin actin-bundling protein 3, testicular"	FSCN3	29999	ENSG00000106328			Fscn3 (MGI:1890386)			
chr7	127610291	127618191	7q32	7q32.1		167413	"PAX4, MODY9, KPD"	Paired box homeotic gene-4	PAX4	5078	ENSG00000106331		"{Diabetes mellitus, ketosis-prone, susceptibility to}, 612227 (3), Autosomal recessive, Autosomal dominant; Diabetes mellitus, type 2, 125853 (3), Autosomal dominant; Maturity-onset diabetes of the young, type IX, 612225 (3)"	Pax4 (MGI:97488)			
chr7	127651988	128092608	7q31.3	7q32.1		602181	"P100, SND1"	EBNA-2 coactivator p100	SND1	27044	ENSG00000197157			Snd1 (MGI:1929266)			
chr7	128027070	128032106	7q32.1	7q32.1		610486	LRRC4	Leucine-rich repeat-containing protein 4	LRRC4	64101	ENSG00000128594			Lrrc4 (MGI:2182081)			
chr7	128241200	128257628	7q31.3	7q32.1		164160	"LEP, OB, LEPD"	Leptin (murine obesity homolog)	LEP	3952	ENSG00000174697	in mouse cen-Cola-2-Met-ob-Cpa-Tcrb-tel	"Obesity, morbid, due to leptin deficiency, 614962 (3), Autosomal recessive"	Lep (MGI:104663)			
chr7	128304172	128343914	7q32.1	7q32.1		612074	"RBM28, ANES"	RNA-binding motif protein 28	RBM28	55131	ENSG00000106344	mutation identified in 1 ANES family	"?Alopecia, neurologic defects, and endocrinopathy syndrome, 612079 (3), Autosomal recessive"	Rbm28 (MGI:2655711)			
chr7	128392276	128409988	7q31.3-q32	7q32.1		146690	"IMPDH1, RP10, LCA11"	"Inosine-5'-monophosphate dehydrogenase, type I"	IMPDH1	3614	ENSG00000106348	pseudogene on 16p13.13	"Leber congenital amaurosis 11, 613837 (3); Retinitis pigmentosa 10, 180105 (3), Autosomal dominant"	Impdh1 (MGI:96567)			
chr7	128455829	128458417	7q32.1	7q32.1		617905	"HILPDA, HIG2"	Hypoxia-inducible lipid droplet-associated protein	HILPDA	29923	ENSG00000135245			Hilpda (MGI:1916823)			
chr7	128739291	128773422	7q32	7q32.1		603420	CALU	Calumenin	CALU	813	ENSG00000128595			Calu (MGI:1097158)			
chr7	128772488	128775789	7q31.3-q32	7q32.1		613522	"OPN1SW, BCP, CBT"	"Blue cone pigment (opsin 1, short-wave-sensitive)"	OPN1SW	611	ENSG00000128617		"Colorblindness, tritan, 190900 (3), Autosomal dominant"	Opn1sw (MGI:99438)			
chr7	128790761	128822132	7q31-q32	7q32.1		611902	"CCDC136, NAG6, KIAA1793"	Coiled-coil domain-containing protein 136	CCDC136	64753	ENSG00000128596			Ccdc136 (MGI:1918128)			
chr7	128830428	128859273	7q32	7q32.1		102565	"FLNC, FLN2, ABPA, ABPL, MFM5, MPD4, CMH26, RCM5"	Filamin C (actin-binding protein-280)	FLNC	2318	ENSG00000128591		"Cardiomyopathy, familial hypertrophic, 26 (3); Cardiomyopathy, familial restrictive 5, 617047 (3), Autosomal dominant; Myopathy, distal, 4, 614065 (3), Autosomal dominant; Myopathy, myofibrillar, 5, 609524 (3), Autosomal dominant"	Flnc (MGI:95557)			
chr7	128870644	128910718	7q32.3	7q32.1		609344	KCP	Kielin/chordin-like protein	KCP	375616	ENSG00000135253			Kcp (MGI:2141640)			
chr7	128937031	128950041	7q32	7q32.1		607218	"IRF5, IBD14, SLEB10"	Interferon regulatory factor 5	IRF5	3663	ENSG00000128604		"{Inflammatory bowel disease 14}, 612245 (3); {Systemic lupus erythematosus, susceptibility to, 10}, 612251 (3)"	Irf5 (MGI:1350924)			
chr7	128954179	129055172	7q32.1	7q32.1		610032	"TNPO3, TRNSR, LGMD1F"	Transportin 3	TNPO3	23534	ENSG00000064419		"Muscular dystrophy, limb-girdle, type 1F, 608423 (3), Autosomal dominant"	Tnpo3 (MGI:1196412)			
chr7	129144715	129169693	7q32.1	7q32.1		610120	"TSPAN33, PEN"	Tetraspanin 33	TSPAN33	340348	ENSG00000158457			Tspan33 (MGI:1919012)			
chr7	129188871	129213547	7q31-q32	7q32.1		601500	"SMOH, SMO, CRJS"	"Smoothened, Drosophila, homolog of"	SMO	6608	ENSG00000128602		"Basal cell carcinoma, somatic, 605462 (3); Curry-Jones syndrome, somatic mosaic, 601707 (3)"	Smo (MGI:108075)			
chr7	129225013	129430210	7q32.1	7q32.1		616520	AHCYL2	Adenosylhomocysteinase-like 2	AHCYL2	23382	ENSG00000158467			Ahcyl2 (MGI:1921590)			
chr7	129434432	129488398	7q32.1	7q32.1		617919	"STRIP2, FAR11B, FAM40B"	Striatin-interacting protein 2	STRIP2	57464	ENSG00000128578						
chr7	129600000	152800000	7q32.2-q36.1			146450	HYSP3	"Hypospadias 3, autosomal"		100689211		between D7S2519 and D7S2442.	"Hypospadias 3, autosomal, 146450 (2), Autosomal dominant, Multifactorial"				
chr7	129611701	129757081	7q32	7q32.2		600879	NRF1	Nuclear respiratory factor 1	NRF1	4899	ENSG00000106459	earlier location = 7q31		Nrf1 (MGI:1332235)			
chr7	129770382	129770491	7q32.2	7q32.2		611607	"MIR182, MIRN182"	Micro RNA 182	MIR182	406958							
chr7	129774691	129774768	7q32.2	7q32.2		611606	"MIR96, MIRN96, DFNA50"	Micro RNA 96	MIR96	407053			"Deafness, autosomal dominant 50, 613074 (3), Autosomal dominant"				
chr7	129774904	129775013	7q32.2	7q32.2		611608	"MIR183, MIRN183"	Micro RNA 183	MIR183	406959							
chr7	129830731	129952959	7q32	7q32.2		601082	"UBE2H, UBCH2, UBC8"	Ubiquitin-conjugating enzyme E2H (homologous to yeast UBC8)	UBE2H	7328	ENSG00000186591			Ube2h (MGI:104632)			
chr7	130070508	130135719	7q32.2	7q32.2		615152	"KLHDC10, SLIM"	KELCH domain-containing protein 10	KLHDC10	23008	ENSG00000128607			Klhdc10 (MGI:1924038)			
chr7	130266862	130289797	7q32	7q32.2		600688	CPA2	"Carboxypeptidase A2, pancreatic"	CPA2	1358	ENSG00000158516			Cpa2 (MGI:3617840)			
chr7	130293133	130324179	7q32	7q32.2		607635	"CPA4, CPA3"	Carboxypeptidase A4	CPA4	51200	ENSG00000128510			Cpa4 (MGI:1919041)			
chr7	130380370	130388107	7q32-qter	7q32.2		114850	CPA1	Carboxypeptidase A	CPA1	1357	ENSG00000091704	both CPA and TRY1 = serine proteases		Cpa1 (MGI:88478)			
chr7	130393770	130441209	7q32	7q32.2		610523	"CEP41, TSGA14, JBTS15"	"Centrosomal protein, 41kD"	CEP41	95681	ENSG00000106477		"Joubert syndrome 15, 614464 (3), Autosomal recessive"	Cep41 (MGI:1891414)			
chr7	130486174	130506296	7q32	7q32.2		601029	"MEST, PEG1"	"Mesoderm specific transcript, mouse, homolog of"	MEST	4232	ENSG00000106484	imprinted maternally		Mest (MGI:96968)			
chr7	130506237	130668757	7q32	7q32.2		604355	COPG2	"Coatomer protein complex, subunit gamma-2"	COPG2	26958	ENSG00000158623			Copg2 (MGI:1858683)			
chr7	130543452	130546899	7q32	7q32.2		610581	"COPG2IT1, CIT1"	"Coatomer protein complex, subunit gamma-2, intronic transcript 1"	COPG2IT1	53844							
chr7	130732553	130734032	7q32.2	7q32.2		609393	"LKF14, BTEB5"	Kruppel-like factor 14	KLF14	136259	ENSG00000266265			Klf14 (MGI:3577024)			
chr7	130800000	132900000	7q32.3			606641	BMIQ1	Body mass index quantitative trait locus 1	BMIQ1	170815		max lod at D7S1804	"[Body mass index QTL1], 606641 (2)"				
chr7	130876746	130876809	7q32.3	7q32.3		610782	"MIR29A, MIRN29A"	Micro RNA 29A	MIR29A	407021							
chr7	130877458	130877538	7q32.3	7q32.3		610783	"MIR29B1, MIRN29B1"	Micro RNA 29B1	MIR29B1	407024							
chr7	131110095	131496638	7q32	7q32.3		605623	MKLN1	Muskelin 1	MKLN1	4289	ENSG00000128585			Mkln1 (MGI:1351638)			
chr7	131500261	131556616	7q32-q33	7q32.3		602632	"PODXL, PCLP"	Podocalyxin-like	PODXL	5420	ENSG00000128567						
chr7	132123331	132648687	7q32.3	7q32.3		604280	PLXNA4	Plexin A4	PLXNA4	91584	ENSG00000221866			Plxna4 (MGI:2179061)			
chr7	132784861	133082157	7q32.3-q33	7q32-q33		613748	CHCHD3	Coiled-coil-helix-coiled-coil-helix domain-containing protein 3	CHCHD3	54927	ENSG00000106554			Chchd3 (MGI:1913325)			
chr7	133253066	134067136	7q31	7q33		608185	"EXOC4, SEC8, KIAA1699"	Exocyst complex component 4	EXOC4	60412	ENSG00000131558			Exoc4 (MGI:1096376)			
chr7	134127351	134282474	7q33	7q33		616478	LRGUK	Leucine-rich repeats- and guanylate kinase domain-containing protein	LRGUK	136332	ENSG00000155530			Lrguk (MGI:1921604)			
chr7	134289336	134320306	7q33	7q33		610923	SLC35B4	"Solute carrier family 35 (UDP-xylose/UDP-N-acetylglucosamine transporter), member B4"	SLC35B4	84912	ENSG00000205060			Slc35b4 (MGI:1931249)			
chr7	134442349	134459238	7q35	7q33		103880	"AKR1B1, ALDR1"	"Aldo-keto reductase family 1, member B1"	AKR1B1	231	ENSG00000085662			Akr1b3 (MGI:1353494)			
chr7	134527591	134541413	7q33	7q33		604707	"AKR1B10, ARL1"	"Aldo-keto reductase family 1, member B10"	AKR1B10	57016	ENSG00000198074			Akr1b8 (MGI:107673)			
chr7	134549096	134579842	7q33	7q33		616336	"AKR1B15, AKR1B10L, AKR1R1B7"	"Aldo-keto reductase family 1, member B15"	AKR1B15	441282	ENSG00000227471						
chr7	134646778	134679815	7q31-q34	7q33		613896	BPGM	"2,3-bisphosphoglycerate mutase"	BPGM	669	ENSG00000172331		"Erythrocytosis due to bisphosphoglycerate mutase deficiency, 222800 (3), Autosomal recessive"	Bpgm (MGI:1098242)			
chr7	134779412	134970728	7q33	7q33		114213	"CALD1, CDM"	Caldesmon-1	CALD1	800	ENSG00000122786						
chr7	134986138	135135781	7q33	7q33		617346	"AGBL3, CCP3"	ATP/GTP-binding protein-like 3	AGBL3	340351	ENSG00000146856			Agbl3 (MGI:1923473)			
chr7	135092302	135170825	7q33	7q33		616980	"C7orf49, MRI"	Chromosome 7 open reading frame 49	CYREN	78996	ENSG00000122783			3110062M04Rik (MGI:1925662)			
chr7	135183837	135211563	7q33	7q33		616303	"WDR91, SORF1"	WD repeat-containing protein 91	WDR91	29062	ENSG00000105875			Wdr91 (MGI:2141558)			
chr7	135231978	135258660	7q31	7q33		609987	STRA8	"Stimulated by retinoic acid 8, mouse, homolog of"	STRA8	346673	ENSG00000146857			Stra8 (MGI:107917)			
chr7	135361794	135510126	7q22-qter	7q33		604911	"CNOT4, NOT4"	"CCR4-NOT transcription complex, subunit 4"	CNOT4	4850	ENSG00000080802			Cnot4 (MGI:1859026)			
chr7	135557913	135648752	7q33	7q33		614352	"NUP205, C7orf14, KIAA0225, NPHS13"	"Nucleoporin, 205kD"	NUP205	23165	ENSG00000155561	mutation identified in 1 NPHS13 family	"?Nephrotic syndrome, type 13, 616893 (3)"	Nup205 (MGI:2141625)			
chr7	135681236	135728203	7q33	7q33		604309	"SLC13A4, SUT1"	"Solute carrier family 13 (sodium/sulfate symporters), member 4 (sulfate transporter 1)"	SLC13A4	26266	ENSG00000164707			Slc13a4 (MGI:2442367)			
chr7	135926754	135977455	7q33	7q33		611050	"LUZP6, MPD6"	Leucine zipper protein 6	LUZP6	767558	ENSG00000267697						
chr7	135926754	135977455	7q33-q35	7q33		606484	MTPN	Myotrophin	MTPN	136319	ENSG00000105887			Mtpn (MGI:99445)			
chr7	136868636	137020254	7q35-q36	7q33		118493	CHRM2	"Cholinergic receptor, muscarinic, 2"	CHRM2	1129	ENSG00000181072			Chrm2 (MGI:88397)			
chr7	136903166	136903293	7q33	7q33		616972	MIR490	Micro RNA 490	MIR490	574443							
chr7	137227340	137343989	7q33	7q33		162095	"PTN, NEGF1"	"Pleiotrophin (heparin binding growth factor 8, neurite growth-promoting factor 1)"	PTN	5764	ENSG00000105894			Ptn (MGI:97804)			
chr7	137384400	137846863	7q32.3-q33	7q33		604072	DGKI	"Diacylglycerol kinase, iota, 130-kD"	DGKI	9162	ENSG00000157680			Dgki (MGI:2443430)			
chr7	137874978	138002100	7q33	7q33		608834	"CREB3L2, BBF2H7"	cAMP response element-binding protein 3-like 2	CREB3L2	64764	ENSG00000182158			Creb3l2 (MGI:2442695)			
chr7	138076431	138118303	7q32-q33	7q33		604741	"AKR1D1, SRD5B1, CBAS2"	"Bile acid synthesis defect, congenital, 2"	AKR1D1	6718	ENSG00000122787		"Bile acid synthesis defect, congenital, 2, 235555 (3), Autosomal recessive"	Akr1d1 (MGI:2384785)			
chr7	138460333	138585587	7q32-q34	7q33-q34		603406	"TRIM24, TIF1, TIF1A, PTC6"	Tripartite motif-containing protein 24 (Transcriptional intermediary factor 1)	TRIM24	8805	ENSG00000122779	fused with RET to form PTC6		Trim24 (MGI:109275)			
chr7	138500000	159345973	7q34-q36			603098	DFNB13	"Deafness, autosomal recessive 13"	DFNB13	1705			"Deafness, autosomal recessive 13, 603098 (2), Autosomal recessive"				
chr7	138500000	159345973	7q34-q36			182960	DHMN1	"Neuronopathy, distal hereditary motor, type I"				between D7S2513 and D7S637	"Neuronopathy, distal hereditary motor, type I, 182960 (2), Autosomal dominant"				
chr7	138500000	159345973	7q34-q36			605727	OTSC2	Otosclerosis 2	OTSC2	93999			"Otosclerosis 2, 605727 (2)"				
chr7	138500000	143400000	7q34			615449	TRBJ@	T-cell receptor beta chain joining gene cluster									
chr7	138500000	143400000	7q34			615446	TRBV@	T-cell receptor beta chain variable gene cluster									
chr7	138591688	138701546	7q34	7q34		611700	SVOPL	SV2-related protein-like	SVOPL	136306	ENSG00000157703			Svopl (MGI:2444335)			
chr7	138706293	138799838	7q33-q34	7q34		605239	"ATP6V0A4, ATP6N1B, VPP2, RTA1C, RTADR"	"ATPase, H+ transporting, lysosomal V0 subunit a isoform 4"	ATP6V0A4	50617	ENSG00000105929		"Renal tubular acidosis, distal, autosomal recessive, 602722 (3)"	Atp6v0a4 (MGI:2153480)			
chr7	138831376	138981625	7q34	7q34		613344	KIAA1549	KIAA1549 gene	KIAA1549	57670	ENSG00000122778			D630045J12Rik (MGI:2669829)			
chr7	139043518	139109718	7q34	7q34		607312	"ZC3HAV1, ZAP, FLJ13288, FLB6421"	Zinc finger CCCH domain-containing antiviral protein 1	ZC3HAV1	56829	ENSG00000105939			Zc3hav1 (MGI:1926031)			
chr7	139133743	139191985	7q34	7q34		617453	"TTC26, IFT56"	Tetratricopeptide repeat domain-containing protein 26	TTC26	79989	ENSG00000105948			Ttc26 (MGI:2444853)			
chr7	139228407	139329420	7q34	7q34		613841	UBN2	Ubinuclein 2	UBN2	254048	ENSG00000157741			Ubn2 (MGI:2444236)			
chr7	139340358	139423456	7q34	7q34		613056	LUC7L2	"Luc7, S. cerevisiae, homolog of, 2"	LUC7L2	51631	ENSG00000146963			Luc7l2 (MGI:2183260)			
chr7	139561569	139777893	7q33-q34	7q34		606868	HIPK2	Homeodomain-interacting protein kinase 2	HIPK2	28996	ENSG00000064393			Hipk2 (MGI:1314872)			
chr7	139778247	140020324	7q34	7q34		274180	"TBXAS1, GHOSAL, CYP5, BDPLT14"	"Thromboxane A synthase 1, platelet"	TBXAS1	6916	ENSG00000059377		"Ghosal hematodiaphyseal syndrome, 231095 (3), Autosomal recessive; ?Thromboxane synthase deficiency, 614158 (1), Autosomal dominant"	Tbxas1 (MGI:98497)			
chr7	140023743	140063720	7q34	7q34		612481	"PARP12, ZC3HDC1, FLJ22693"	"Poly(ADP-ribose) polymerase family, member 12"	PARP12	64761	ENSG00000059378			Parp12 (MGI:2143990)			
chr7	140719326	140924927	7q34	7q34		164757	"BRAF, NS7"	Murine sarcoma viral (v-raf) oncogene homolog B1	BRAF	673	ENSG00000157764	pseudogene BRAF2 on Xq13 or 7q	"Adenocarcinoma of lung, somatic, 211980 (3); Cardiofaciocutaneous syndrome, 115150 (3), Autosomal dominant; Colorectal cancer, somatic (3); LEOPARD syndrome 3, 613707 (3), Autosomal dominant; Melanoma, malignant, somatic (3); Nonsmall cell lung cancer, somatic (3); Noonan syndrome 7, 613706 (3), Autosomal dominant"	Braf (MGI:88190)			
chr7	141006160	141014980	7q32-q34	7q34		611993	MRPS33	Mitochondrial ribosomal protein S33	MRPS33	51650	ENSG00000090263	4 pseudogenes		Mrps33 (MGI:1338046)			
chr7	141551277	141662152	7q34	7q34		610345	"AGK, MULK, MTDPS10, CATC5, CTRCT38"	Acylglycerol kinase	AGK	55750	ENSG00000006530		"Cataract 38, autosomal recessive, 614691 (3), Autosomal recessive; Sengers syndrome, 212350 (3), Autosomal recessive"	Agk (MGI:1917173)			
chr7	141708352	141731270	7q34	7q34		614084	"WEE2, WEE1B"	"Wee1, S. pombe, homolog of, 2"	WEE2	494551	ENSG00000214102			Wee2 (MGI:3027899)			
chr7	141738320	141750487	7q34	7q34		600439	"SSBP1, SSBP"	Single-stranded DNA-binding protein 1	SSBP1	6742	ENSG00000106028			Ssbp1 (MGI:1920040)			
chr7	141764096	141765196	7q31.3-q32	7q34		604868	"TAS2R3, T2R3"	"Taste receptor type 2, member 3"	TAS2R3	50831	ENSG00000127362			Tas2r137 (MGI:3606604)			
chr7	141778488	141779387	7q31.3-q32	7q34		604869	"TAS2R4, T2R4"	"Taste receptor type 2, member 4"	TAS2R4	50832	ENSG00000127364			Tas2r108 (MGI:2681210)			
chr7	141790216	141791365	7q31.3-q32	7q34		605062	"TAS2R5, T2R5"	"Taste receptor type 2, member 5"	TAS2R5	54429	ENSG00000127366						
chr7	141927355	141947008	7q33	7q34		604987	"CLEC5A, CLECSF5, MDL1"	"C-type lectin domain family 5, member A"	CLEC5A	23601	ENSG00000258227			Clec5a (MGI:1345151)			
chr7	141972630	141973772	7q34	7q34		607751	"TAS2R38, T2R61, PTC"	"Taste receptor, type 2, member 38"	TAS2R38	5726	ENSG00000257138		"[Phenylthiocarbamide tasting], 171200 (3), Autosomal dominant"	Tas2r138 (MGI:2681306)			
chr7	141986516	142106746	7q34	7q34		154360	"MGAM, MGA"	Maltase-glucoamylase	MGAM	8972	ENSG00000257335	similar to EST GS1365		Mgam (MGI:1203495)			
chr7	142740234	142753075	7q35	7q34		276000	"PRSS1, TRY1"	"Protease, serine, 1 (trypsin 1)"	PRSS1	5644	ENSG00000204983	8 trypsinogen genes embedded in TCRB locus	"Pancreatitis, hereditary, 167800 (3), Autosomal dominant; Trypsinogen deficiency, 614044 (1), Autosomal recessive"	Try10 (MGI:3687012)			
chr7	142770942	142774563	7q35	7q34		601564	"PRSS2, TRY2"	"Protease, serine, 2 (trypsin 2)"	PRSS2	5645	ENSG00000275896		"{Pancreatitis, chronic, protection against}, 167800 (3), Autosomal dominant"	Prss2 (MGI:102759)			
chr7	142786212	142786223	7q34	7q34		615447	TRBD1	T-cell receptor beta chain diversity gene 1	TRBD1	28637							
chr7	142791693	142793140	7q34	7q34		186930	TRBC1	T-cell receptor beta chain constant region 1	TRBC1	28639							
chr7	142795704	142795719	7q34	7q34		615448	TRBD2	T-cell receptor beta chain diversity gene 2	TRBD2	28636							
chr7	142801040	142802528	7q34	7q34		615445	TRBC2	T-cell receptor beta chain constant region 2	TRBC2	28638							
chr7	142854638	142871092	7q33-q35	7q34		602757	"EPHB6, HEP"	Ephrin receptor EPHB6	EPHB6	2051	ENSG00000106123			Ephb6 (MGI:1096338)			
chr7	142871202	142885744	7q33-q34	7q34		606680	"TRPV6, ECAC2, CAT1, CATL"	"Transient receptor potential cation channel, subfamily V, member 6"	TRPV6	55503	ENSG00000165125			Trpv6 (MGI:1927259)			
chr7	142908100	142933722	7q35	7q34		606679	"TRPV5, ECAC1, CAT2"	"Transient receptor potential cation channel, subfamily V, member 5"	TRPV5	56302	ENSG00000127412			Trpv5 (MGI:2429764)			
chr7	142941113	142962415	7q33	7q34		613883	KEL	Kell blood group	KEL	3792	ENSG00000197993		"[Blood group, Kell], 110900 (3)"	Kel (MGI:1346053)			
chr7	143132080	143139740	7q32-q36	7q34		176720	PIP	Prolactin-inducible protein	PIP	5304	ENSG00000159763			Pip (MGI:102696)			
chr7	143222036	143223078	7q34	7q34		613964	"TAS2R40, T2R40"	"Taste receptor, type 2, member 40"	TAS2R40	259286	ENSG00000221937			Tas2r144 (MGI:2681312)			
chr7	143263428	143269128	7q34	7q34		602321	GSTK1	"Glutathione S-transferase, kappa-1"	GSTK1	373156	ENSG00000197448			Gstk1 (MGI:1923513)			
chr7	143284898	143288048	7q34	7q34		616524	TMEM139	Transmembrane protein 139	TMEM139	135932	ENSG00000178826			Tmem139 (MGI:1924444)			
chr7	143288214	143307695	7q35	7q34		600639	"CASP2, NEDD2, ICH1"	"Caspase 2, apoptosis-related cysteine protease (neural precursor cell expressed, developmentally down-regulated 2)"	CASP2	835	ENSG00000106144			Casp2 (MGI:97295)			
chr7	143316125	143352007	7q35	7q34		118425	CLCN1	"Chloride channel-1, skeletal muscle"	CLCN1	1180	ENSG00000188037		"Myotonia congenita, dominant, 160800 (3), Autosomal dominant; Myotonia congenita, recessive, 255700 (3), Autosomal recessive; Myotonia levior, recessive (3)"	Clcn1 (MGI:88417)			
chr7	143381226	143391110	7q34-q35	7q34		602002	ZYX	Zyxin	ZYX	7791	ENSG00000159840			Zyx (MGI:103072)			
chr7	143390812	143408891	7q32-q36	7q34-q35		179610	"EPHA1, EPHT1"	eph tyrosine kinase 1 (erythropoietin-producing hepatoma amplified sequence; oncogene EPH; ephrin receptor EphA1)	EPHA1	2041	ENSG00000146904			Epha1 (MGI:107381)			
chr7	143400000	159345973	7q35-q36			157570	"D7S437, MS3315"	Minisatellite 33.15									
chr7	143400000	159345973	7q35-q36			600510	"GPDS1, PDS1"	Glaucoma-related pigment dispersion syndrome-1	GPDS1	7986			"Pigment dispersion syndrome, 600510 (2), Autosomal dominant"				
chr7	143400000	159345973	7q35-q36			612514	SLI4	Specific language impairment 4		100233227		associated with rs1723629	"{Specific language impairment 4}, 612514 (2)"				
chr7	143443452	143444408	7q35	7q35		613968	"TAS2R60, T2R60"	"Taste receptor, type 2, member 60"	TAS2R60	338398	ENSG00000185899			Tas2r135 (MGI:2681302)			
chr7	143477872	143478795	7q35	7q35		613965	"TAS2R41, T2R59"	"Taste receptor, type 2, member 41"	TAS2R41	259287	ENSG00000221855			Tas2r126 (MGI:2681273)			
chr7	143620951	143730085	7q35	7q35		616252	"TCAF2, FAM115C, FAM139A"	TRPM8 channel-associated factor 2	TCAF2	285966	ENSG00000170379			Tcaf2 (MGI:2385258)			
chr7	143851367	143902197	7q35	7q35		616251	"TCAF1, FAM115A, KIAA0738"	TRPM8 channel-associated factor 1	TCAF1	9747	ENSG00000198420			Tcaf1 (MGI:1914665)			
chr7	143907151	143988539	7q35	7q35		608497	"OR2F1, OLF3"	"Olfactory receptor, family 2, subfamily F, member 1"	OR2F1	26211	ENSG00000213215			Olfr453 (MGI:3030287)			
chr7	144355395	144380631	7q33-q35	7q35		600888	"ARHGEF5, TIM"	Rho guanine nucleotide exchange factor-5 (oncogene TIM)	ARHGEF5	7984	ENSG00000050327			Arhgef5 (MGI:1858952)			
chr7	144396804	144410421	7q35	7q35		610934	"NOBOX, POF5"	"Newborn ovary homeobox, mouse, homolog of"	NOBOX	135935	ENSG00000106410		"Premature ovarian failure 5, 611548 (3), Autosomal dominant"	Nobox (MGI:108011)			
chr7	144451940	144836423	7q34	7q35		606370	"TPK1, THMD5"	Thiamine pyrophosphokinase	TPK1	27010	ENSG00000196511		"Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), 614458 (3), Autosomal recessive"	Tpk1 (MGI:1352500)			
chr7	146116206	148420997	7q35-q36	7q35-q36		604569	"CNTNAP2, CASPR2, NRXN4, CDFE, AUTS15, PTHSL1"	Contactin-associated protein-like 2	CNTNAP2	26047	ENSG00000174469		"{Autism susceptibility 15}, 612100 (3); Cortical dysplasia-focal epilepsy syndrome, 610042 (3), Autosomal recessive; Pitt-Hopkins like syndrome 1, 610042 (3), Autosomal recessive"	Cntnap2 (MGI:1914047)			
chr7	148200000	159345973	7q36			605967	ACRPS	Acropectoral syndrome		85505			"Acropectoral syndrome, 605967 (2), Autosomal dominant"				
chr7	148200000	159345973	7q36			609636	AD10	Alzheimer disease-10		780912		max lod with D7S798	"Alzheimer disease-10, 609636 (2), Autosomal dominant"				
chr7	148200000	159345973	7q36			611016	AUTS10	"Autism, susceptibility to, 10"				max lod at D7S483	"{Autism, susceptibility to, 10}, 611016 (2)"				
chr7	148698156	148801109	7q36.1	7q36.1		603134	CUL1	Cullin 1	CUL1	8454	ENSG00000055130			Cul1 (MGI:1349658)			
chr7	148807371	148884348	7q35	7q36.1		601573	"EZH2, EZH1, WVS"	"Enhancer of zeste, Drosophila, homolog of, 2"	EZH2	2146	ENSG00000106462	pseudogene on 21q22	"Weaver syndrome, 277590 (3), Autosomal dominant"	Ezh2 (MGI:107940)			
chr7	148941487	148941570	7q36	7q36.1		601824	"RNY5, Y5"	"RNA, Y5 small cytoplasmic"	RNY5	6090							
chr7	148963314	148963409	7q36	7q36.1		601823	"RNY4, Y4"	"RNA, Y4 small cytoplasmic"	RNY4	6086							
chr7	148983754	148983855	7q36	7q36.1		601822	"RNY3, Y3"	"RNA, Y3 small cytoplasmic"	RNY3	6085							
chr7	148987135	148987247	7q36	7q36.1		601821	"RNY1, Y1"	"RNA, Y1 small cytoplasmic"	RNY1	6084							
chr7	149195461	149226247	7q36.1	7q36.1		603397	"ZNF282, HUB1"	Zinc finger protein 282	ZNF282	8427	ENSG00000170265			Zfp282 (MGI:2141413)			
chr7	149239650	149255608	7q36.1	7q36.1		602386	"ZNF212, ZNFC150, ZNF182"	Zinc finger protein 212	ZNF212	7988	ENSG00000170260			Zfp212 (MGI:2682609)			
chr7	149472792	149497831	7q36.1	7q36.1		613914	"ZNF746, PARIS"	Zinc finger protein 746	ZNF746	155061	ENSG00000181220			Zfp746 (MGI:1916478)			
chr7	149764181	149776322	7q36.1	7q36.1		614040	"ZNF467, EZI, ZFP467"	Zinc finger protein 467	ZNF467	168544	ENSG00000181444			Zfp467 (MGI:1916160)			
chr7	149776041	149833964	7q36.1	7q36.1		617356	SSPO	Subcommissural organ spondin	SSPO	23145	ENSG00000197558			Sspo (MGI:2674311)			
chr7	149872967	149880712	7q36	7q36.1		611019	ATP6V0E2	"ATPase, H+ transporting, lysosomal, 9kD, V- subunit E2"	ATP6V0E2	155066	ENSG00000171130			Atp6v0e2 (MGI:1923502)			
chr7	150041354	150045371	7q36.1	7q36.1		615171	LOC100134040	LOC100134040 gene		100134040							
chr7	150329848	150332720	7q36.1	7q36.1		615252	"ZBED6CL, C7orf29"	ZBED6 C terminus-like protein	ZBED6CL	113763	ENSG00000188707						
chr7	150338317	150341684	7q36.1	7q36.1		601973	"RARRES2, TIG2"	Retinoic acid receptor responder 2	RARRES2	5919	ENSG00000106538			Rarres2 (MGI:1918910)			
chr7	150450629	150479394	7q36.1	7q36.1		616962	GIMAP8	"GTPase, IMAP family, member 8"	GIMAP8	155038	ENSG00000171115			Gimap8 (MGI:2685303)			
chr7	150514856	150521072	7q36.1	7q36.1		616961	GIMAP7	"GTPase IMAP family, member 7"	GIMAP7	168537	ENSG00000179144			Gimap7 (MGI:1349657)			
chr7	150567369	150573954	7q36.1	7q36.1		608087	"GIMAP4, IMAP4, IAN1"	"GTPase, IMAP family, member 4"	GIMAP4	55303	ENSG00000133574			Gimap4 (MGI:1349656)			
chr7	150625374	150632647	7q36.1	7q36.1		616960	GIMAP6	"GTPase, IMAP family, member 6"	GIMAP6	474344	ENSG00000133561			Gimap6 (MGI:1918876)			
chr7	150685705	150693640	7q36.1	7q36.1		608085	"GIMAP2, IMAP2"	"GTPase, IMAP family, member 2"	GIMAP2	26157	ENSG00000106560						
chr7	150716556	150724279	7q36.1	7q36.1		608084	"GIMAP1, IMAP1"	"GTPase, IMAP family, member 1"	GIMAP1	170575	ENSG00000213203			Gimap1 (MGI:109368)			
chr7	150737347	150743648	7q36.1	7q36.1		608086	"GIMAP5, IAN4L1, IMAP3"	"GTPase, IMAP family, member 5"	GIMAP5	55340	ENSG00000196329						
chr7	150791286	150801359	7q36.1	7q36.1		610385	LR8	LR8 protein	TMEM176B	28959	ENSG00000106565			Tmem176b (MGI:1916348)			
chr7	150800542	150805119	7q36.1	7q36.1		610334	"TEM176A, HCA112, GS188"	Transmembrane protein 176A	TMEM176A	55365	ENSG00000002933			Tmem176a (MGI:1913308)			
chr7	150824874	150861290	7q31-q32	7q36.1		104610	ABP1	Amiloride-binding protein-1	AOC1	26	ENSG00000002726			Aoc1 (MGI:1923757)			
chr7	150944955	150978313	7q35-q36	7q36.1		152427	"KCNH2, LQT2, HERG, SQT1"	"Potassium voltage-gated channel, subfamily H, member 2 (human ether-a-go-go-related gene)"	KCNH2	3757	ENSG00000055118		"Long QT syndrome 2, 613688 (3), Autosomal dominant; {Long QT syndrome 2, acquired, susceptibility to}, 613688 (3), Autosomal dominant; Short QT syndrome 1, 609620 (3)"	Kcnh2 (MGI:1341722)			
chr7	150991055	151014598	7q36	7q36.1		163729	NOS3	"Nitric oxide synthase 3, endothelial cell"	NOS3	4846	ENSG00000164867		"{Alzheimer disease, late-onset, susceptibility to}, 104300 (3), Autosomal dominant; {Coronary artery spasm 1, susceptibility to} (3); {Hypertension, pregnancy-induced}, 189800 (3), Autosomal dominant; {Hypertension, susceptibility to}, 145500 (3), Multifactorial; {Ischemic stroke, susceptibility to}, 601367 (3), Multifactorial; {Placental abruption} (3)"	Nos3 (MGI:97362)			
chr7	151012208	151028266	7q36.1	7q36.1		612205	"ATG9B, NOS3AS, APG9L2, SONE"	"Autophagy 9, S. cerevisiae, homolog of, B"	ATG9B	285973	ENSG00000181652			Atg9b (MGI:2685420)			
chr7	151028421	151047781	7q35-q36	7q36.1		605464	"ABCB8, MABC1"	"ATP-binding cassette, subfamily B, member 8"	ABCB8	11194	ENSG00000197150			Abcb8 (MGI:1351667)			
chr7	151048291	151052755	7q35	7q36.1		611741	"ACCN3, ASIC3, TNAC1, DRASIC"	"Cation channel, amiloride-sensitive, neuronal 3"	ASIC3	9311	ENSG00000213199			Asic3 (MGI:2159339)			
chr7	151053811	151057964	7q36	7q36.1		123831	"CDK5, LIS7"	Cyclin-dependent kinase 5	CDK5	1020	ENSG00000164885	mutation identified in 1 LIS7 family	"?Lissencephaly 7 with cerebellar hypoplasia, 616342 (3), Autosomal recessive"	Cdk5 (MGI:101765)			
chr7	151058199	151076526	7q35-q36	7q36.1		109280	"SLC4A2, AE2, EPB3L1"	"Solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane protein band 3-like 1)"	SLC4A2	6522	ENSG00000164889			Slc4a2 (MGI:109351)			
chr7	151076620	151080882	7q35	7q36.1		606965	"FASTK, FAST"	Fas-activated serine/threonine kinase	FASTK	10922	ENSG00000164896			Fastk (MGI:1913837)			
chr7	151081084	151083532	7q36.1	7q36.1		614792	"TMUB1, DULP, SB144, C7orf21"	Transmembrane and ubiquitin-like domain-containing protein 1	TMUB1	83590	ENSG00000164897			Tmub1 (MGI:1923764)			
chr7	151085830	151144435	7q36.1	7q36.1		616813	"AGAP3, CENTG3, CRAG"	"ARF GTPase-activating protein with GTPase domain, ankyrin repeat, and pleckstrin homology domain 3"	AGAP3	116988	ENSG00000133612			Agap3 (MGI:2183446)			
chr7	151148008	151167547	7q36	7q36.1		603354	GBX1	Gastrulation brain homeobox 1	GBX1	2636	ENSG00000164900			Gbx1 (MGI:95667)			
chr7	151175697	151187831	7q36.1	7q36.1		615054	"ASB10, GLC1F"	Ankyrin repeat- and SOCS box-containing protein 10	ASB10	136371	ENSG00000146926		"Glaucoma 1, open angle, F, 603383 (3)"	Asb10 (MGI:2152836)			
chr7	151207836	151227373	7q36	7q36.1		612510	"ABCF2, HUSSY18"	"ATP-binding cassette, subfamily F, member 2"	ABCF2	10061	ENSG00000033050			Abcf2 (MGI:1351657)			
chr7	151232488	151238826	7q36.1	7q36.1		608037	"CHPF2, KIAA1402, CSGlcAT"	Chondroitin polymerizing factor 2	CHPF2	54480	ENSG00000033100			Chpf2 (MGI:1917522)			
chr7	151238420	151238537	7q36.1	7q36.1		615245	MIR671	Micro RNA 671	MIR671	768213							
chr7	151238972	151277451	7q35-q36	7q36.1		601737	"SMARCD3, BAF60C"	"SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 3"	SMARCD3	6604	ENSG00000082014			Smarcd3 (MGI:1914243)			
chr7	151341698	151378460	7q36.1	7q36.1		607981	NUB1	Negative regulator of ubiquitin-like proteins 1	NUB1	51667	ENSG00000013374			Nub1 (MGI:1889001)			
chr7	151466011	151519923	7q36	7q36.1		601293	"RHEB, RHEB2"	Ras homolog enriched in brain	RHEB	6009	ENSG00000106615			Rheb (MGI:97912)			
chr7	151556113	151877230	7q36	7q36.1		602743	"PRKAG2, WPWS, CMH6"	"Protein kinase, AMP-activated, noncatalytic, gamma-2"	PRKAG2	51422	ENSG00000106617		"Cardiomyopathy, hypertrophic 6, 600858 (3), Autosomal dominant; Glycogen storage disease of heart, lethal congenital, 261740 (3), Autosomal dominant; Wolff-Parkinson-White syndrome, 194200 (3), ?Autosomal dominant"	Prkag2 (MGI:1336153)			
chr7	151956378	152019933	7q36.1	7q36.1		615133	"GALNTL5, GALNACT19"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	GALNTL5	168391	ENSG00000106648			Galntl5 (MGI:1915159)			
chr7	152025654	152122346	7q36.1	7q36.1		615130	"GALNT11, GALNACT11"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	63917	ENSG00000178234			Galnt11 (MGI:2444392)			
chr7	152134924	152436641	7q36	7q36.1		606833	"KMT2C, MLL3, KIAA1506, KLEFS2"	Lysine (K)-specific methyltransferase 2C	KMT2C	58508	ENSG00000055609		"Kleefstra syndrome 2, 617768 (3), Autosomal dominant"	Kmt2c (MGI:2444959)			
chr7	152646497	152676164	7q36.1	7q36.1		600375	"XRCC2, FANCU"	"X-ray repair, complementing defective, repair in Chinese hamster cells-2"	XRCC2	7516	ENSG00000196584	mutation identified in 1 FANCU patient	"?Fanconi anemia, complementation group U, 617247 (3), Autosomal recessive"	Xrcc2 (MGI:1927345)			
chr7	153747985	154894289	7q36.2	7q36.2		126141	"DPP6, VF2, MRD33"	Dipeptidylpeptidase VI	DPP6	1804	ENSG00000130226		"Mental retardation, autosomal dominant 33, 616311 (3); {Ventricular fibrillation, paroxysmal familial, 2}, 612956 (3), Autosomal dominant"	Dpp6 (MGI:94921)			
chr7	154943689	155003418	7q36	7q36.2		608254	"PAXIP1, PAXIP1L, PTIP"	PAX transcription activation domain-interacting protein 1	PAXIP1	22976	ENSG00000157212						
chr7	155070323	155087391	7q36.1	7q36.2		601305	HTR5A	5-hydroxytryptamine (serotonin) receptor-5A	HTR5A	3361	ENSG00000157219			Htr5a (MGI:96283)			
chr7	155200000	159345973	7q36.3			613959	"SCZD16, C16DUPq36.3, DUP7q36.3"	"Chromosome 7q36.3 duplication syndrome, 362kb"				362kb duplication that includes VIPR2	"Schizophrenia 16, 613959 (4)"				
chr7	155297771	155310234	7q36	7q36.3		602055	INSIG1	Insulin-induced gene 1	INSIG1	3638	ENSG00000186480			Insig1 (MGI:1916289)			
chr7	155356987	155367932	7q36	7q36.3		608450	BLACE	B-cell acute lymphoblastic leukemia-expressed gene	BLACE	338436							
chr7	155458128	155464830	7q36	7q36.3		131310	EN2	Engrailed-2	EN2	2020	ENSG00000164778			En2 (MGI:95390)			
chr7	155501257	155533843	7q36.3	7q36.3		612493	CNPY1	"Canopy 1, zebrafish, homolog of"	CNPY1	285888	ENSG00000146910			Cnpy1 (MGI:2442451)			
chr7	155799983	155812272	7q36	7q36.3		600725	"SHH, HPE3, HLP3, SMMCI, MCOPCB5"	Sonic hedgehog	SHH	6469	ENSG00000164690	separate from TPT1	"Holoprosencephaly 3, 142945 (3), Autosomal dominant; Microphthalmia with coloboma 5, 611638 (3), Autosomal dominant; Schizencephaly, 269160 (3); Single median maxillary central incisor, 147250 (3), Autosomal dominant"	Shh (MGI:98297)			
chr7	156638365	156640653	7q36	7q36.3		610242	C7orf13	Chromosome 7 open reading frame 13	C7orf13	129790		overlaps RNF32 on the opposite strand					
chr7	156640201	156678332	7q36	7q36.3		610241	RNF32	RING finger protein 32	RNF32	140545	ENSG00000105982			Rnf32 (MGI:1861747)			
chr7	156669011	156893207	7q36	7q36.3		605522	"LMBR1, ACHP, C7orf2, PPD2, THYP, LSS"	"Limb region 1, mouse, homolog of"	LMBR1	64327	ENSG00000105983		"Acheiropody, 200500 (3), Autosomal recessive; Hypoplastic or aplastic tibia with polydactyly, 188740 (3), Autosomal dominant; Laurin-Sandrow syndrome, 135750 (3), Autosomal dominant; Polydactyly, preaxial type II, 174500 (3), Autosomal dominant; Syndactyly, type IV, 186200 (3), Autosomal dominant; Triphalangeal thumb, type I, 174500 (3), Autosomal dominant; Triphalangeal thumb-polysyndactyly syndrome, 174500 (3), Autosomal dominant"	Lmbr1 (MGI:1861746)			
chr7	156949721	156973181	7q36	7q36.3		611269	"NOM1, C7orf3"	Nucleolar protein with MIF4G domain 1	NOM1	64434	ENSG00000146909			Nom1 (MGI:1861749)			
chr7	157004852	157010652	7q36	7q36.3		142994	"MNX1, HLXB9, HOXHB9, SCRA1"	Motor neuron and pancreas homeobox 1	MNX1	3110	ENSG00000130675		"Currarino syndrome, 176450 (3), Autosomal dominant"	Mnx1 (MGI:109160)			
chr7	157138951	157269371	7q36.3	7q36.3		614454	"UBE3C, HECTH2, KIAA0010, KIAA10"	Ubiquitin protein ligase E3C	UBE3C	9690	ENSG00000009335			Ube3c (MGI:2140998)			
chr7	157337003	157417438	7q36.3	7q36.3		611332	"DNAJB6, MRJ, DJ4, LGMD1E"	"DNAJ/HSP40 homolog, subfamily B, member 6"	DNAJB6	10049	ENSG00000105993	previously assigned to 11q25	"Muscular dystrophy, limb-girdle, type 1E, 603511 (3), Autosomal dominant"	Dnajb6 (MGI:1344381)			
chr7	157539051	158587801	7q36	7q36.3		601698	"PTPRN2, IAR, ICAAR"	"Protein-tyrosine phosphatase, receptor-type, N, polypeptide 2"	PTPRN2	5799	ENSG00000155093			Ptprn2 (MGI:107418)			
chr7	158631168	158704830	7q36.3	7q36.3		608532	"NCAPG2, CAPG2, MTB"	Non-SMC condensin II complex subunit G2	NCAPG2	54892	ENSG00000146918			Ncapg2 (MGI:1923294)			
chr7	158730996	158829627	7q36.3	7q36.3		616691	"ESYT2, FAM62B"	Extended synaptotagmin-like protein 2	ESYT2	57488	ENSG00000117868			Esyt2 (MGI:1261845)			
chr7	158839244	158958694	7q36.3	7q36.3		615462	"WDR60, SRTD8, SRPS6"	WD repeat containing protein 60	WDR60	55112	ENSG00000126870		"Short-rib thoracic dysplasia 8 with or without polydactyly, 615503 (3), Autosomal recessive"	Wdr60 (MGI:2445085)			
chr7	159028174	159144956	7q36.3	7q36.3		601970	VIPR2	Vasoactive intestinal peptide receptor 2	VIPR2	7434	ENSG00000106018			Vipr2 (MGI:107166)			
chr7	0	159345973	Chr.7			608391	"AIS2, VAMAS3"	"Autoimmune disease, susceptibility to, 2"	AIS2	378426			"{Autoimmune disease, susceptibility to, 2}, 608391 (2)"				
chr7	0	159345973	Chr.7			118880	NHCP2	Nonhistone chromosomal protein-2									
chr8	0	19200000	8p23.3-p22			606129	DBA2	Diamond-Blackfan anemia 2		114086			"Diamond-Blackfan anemia 2, 606129 (2)"				
chr8	0	29000000	8p23-p21			612279	GEFSP6	"Generalized epilepsy with febrile seizures plus, type 6"		100190787		between D8S1706 and D8S549	"Epilepsy, generalized, with febrile seizures plus, type 6, 612279 (2)"				
chr8	0	19200000	8p23-p22			148370	KWE	Keratolytic winter erythema	KWE	3896			"Keratolytic winter erythema, 148370 (2), Autosomal dominant"				
chr8	0	12800000	8p23			609259	MYP10	Myopia 10	MYP10	553195			"Myopia 10, 609259 (2), Multifactorial"				
chr8	0	19200000	8p23-p22			615174	TDH	"L-threonine dehydrogenase, pseudogene"	TDH	157739							
chr8	0	12800000	8p23			606662	WS2C	"Waardenburg syndrome, type 2C"		170594			"Waardenburg syndrome, type 2C, 606662 (2)"				
chr8	406807	469875	8p23.3	8p23.3		609098	"FBXO25, FBX25"	F-box only protein 25	FBXO25	26260	ENSG00000147364			Fbxo25 (MGI:1914072)			
chr8	737604	1708475	8p	8p23.3		605438	"DLGAP2, DAP2"	Discs large associated protein 2	DLGAP2	9228	ENSG00000198010			Dlgap2 (MGI:2443181)			
chr8	1755777	1786569	8p23	8p23.3		607837	"CLN8, EPMR"	CLN8 gene	CLN8	2055	ENSG00000182372		"Ceroid lipofuscinosis, neuronal, 8, 600143 (3), Autosomal recessive; Ceroid lipofuscinosis, neuronal, 8, Northern epilepsy variant, 610003 (3), Autosomal recessive"	Cln8 (MGI:1349447)			
chr8	1823975	1958640	8p23	8p23.3		608136	"ARHGEF10, KIAA0294, SNCV"	Rho guanine nucleotide exchange factor 10	ARHGEF10	9639	ENSG00000104728	mutation identified in 1 SNCV family	"?Slowed nerve conduction velocity, AD, 608236 (3), Autosomal dominant"	Arhgef10 (MGI:2444453)			
chr8	2045042	2145455	8p23.3	8p23.3		603509	MYOM2	Myomesin 2	MYOM2	9172	ENSG00000036448			Myom2 (MGI:1328358)			
chr8	2935352	4995034	8p23	8p23.2		608397	"CSMD1, KIAA1890"	Cub and Sushi multiple domains 1	CSMD1	64478	ENSG00000183117			Csmd1 (MGI:2137383)			
chr8	6300000	12800000	8p23.1			222400	DIH2	"Hernia, congenital diaphragmatic 2"		780899			"Hernia, congenital diaphragmatic 2, 222400 (2), Autosomal recessive"				
chr8	6300000	12800000	8p23.1			612254	SLEB12	"Systemic lupus erythematosus, susceptibility to, 12"		100190928		associated with rs13277113	"{Systemic lupus erythematosus, susceptibility to, 12}, 612254 (2)"				
chr8	6406591	6648504	8p23	8p23.1		607117	MCPH1	Microcephalin	MCPH1	79648	ENSG00000147316	genetic heterogeneity	"Microcephaly 1, primary, autosomal recessive, 251200 (3), Autosomal recessive"	Mcph1 (MGI:2443308)			
chr8	6499650	6563419	8p23	8p23.1		601922	"ANGPT2, ANG2"	Angiopoietin 2	ANGPT2	285	ENSG00000091879	close to MCPH1		Angpt2 (MGI:1202890)			
chr8	6708356	6761502	8p23.1	8p23.1		614796	AGPAT5	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5	55326	ENSG00000155189			Agpat5 (MGI:1196345)			
chr8	6870574	6878006	8p23.1	8p23.1		602056	DEFB1	"Defensin, beta-1"	DEFB1	1672	ENSG00000164825						
chr8	6924693	6926075	8p23.1	8p23.1		600471	"DEFA6, DEF6"	"Defensin, alpha-6, Paneth cell-specific"	DEFA6	1671	ENSG00000164822						
chr8	6935819	6938337	8p23	8p23.1		601157	"DEFA4, DEF4, HP4"	"Defensin, alpha-4, corticostatin"	DEFA4	1669	ENSG00000164821						
chr8	6977648	6980119	8p23.1	8p23.1		125220	"DEFA1, DEF1, MRS"	"Defensin, alpha-1, myeloid-related sequence"	DEFA1	1667	ENSG00000206047						
chr8	7055299	7056738	8p23.1	8p23.1		600472	"DEFA5, DEF5"	"Defensin, alpha-5, Paneth cell-specific"	DEFA5	1670	ENSG00000164816						
chr8	7255242	7260475	8p23.1	8p23.1		613051	FAM90A15	"Family with sequence similarity 90, member A15"	FAM90A15P	389630		copy 1					
chr8	7262865	7268097	8p23.1	8p23.1		613042	FAM90A3	"Family with sequence similarity 90, member A3"	FAM90A3P	389611		copy 2					
chr8	7278109	7283341	8p23.1	8p23.1		613049	FAM90A13	"Family with sequence similarity 90, member A13"	FAM90A13P	441314		copy 4					
chr8	7285731	7290963	8p23.1	8p23.1		613043	FAM90A5	"Family with sequence similarity 90, member A5"	FAM90A5P	441315		copy 5					
chr8	7293353	7298583	8p23.1	8p23.1		613054	FAM90A20	"Family with sequence similarity 90, member A20"	FAM90A20P	728430		copy 6					
chr8	7428887	7430347	8p23.1	8p23.1		606611	"DEFB103A, DEFB3, HBD3, HBP3"	"Defensin, beta 103A"	DEFB103B	55894	ENSG00000177243						
chr8	7447753	7463669	8p23-p22	8p23.1		606560	"SPAG11, HE2, EP2"	Sperm-associated antigen 11	SPAG11B	10407	ENSG00000164871			Spag11b (MGI:3647173)			
chr8	7556137	7559103	8p23.1	8p23.1		613044	FAM90A7	"Family with sequence similarity 90, member A7"	FAM90A7P	441317		copy 8					
chr8	7713782	7719014	8p23.1	8p23.1		613050	FAM90A14	"Family with sequence similarity 90, member A14"	FAM90A14P	645651		copy 12					
chr8	7721428	7726662	8p23.1	8p23.1		613052	FAM90A18	"Family with sequence similarity 90, member A18"	FAM90A18P	441326		copy 13					
chr8	7736724	7741957	8p23.1	8p23.1		613045	FAM90A8	"Family with sequence similarity 90, member A8"	FAM90A8P	441324		copy 15					
chr8	7752019	7757253	8p23.1	8p23.1		613053	FAM90A19	"Family with sequence similarity 90, member A19"	FAM90A19P	728753		copy 17					
chr8	7759667	7764901	8p23.1	8p23.1		613046	FAM90A9	"Family with sequence similarity 90, member A9"	FAM90A9P	441327		copy 18					
chr8	7769583	7771312	8p23.1	8p23.1		613047	FAM90A10	"Family with sequence similarity 90, member A10"	FAM90A10P	441328		copy 19					
chr8	7894564	7896715	8p23.1	8p23.1		602215	"DEFB4A, DEFB4, DEFB2"	"Defensin, beta-4a (formerly defensin, beta-2)"	DEFB4A	1673	ENSG00000171711						
chr8	8027073	8032304	8p23.1	8p23.1		613048	FAM90A12	"Family with sequence similarity 90, member A12"	FAM90A12P	645879		copy 22					
chr8	8317730	8386440	8p23.1	8p23.1		617344	"PRAG1, PRAGMIN, NACK"	PEAK1-related kinase-activating pseudokinase 1	PRAG1	157285	ENSG00000275342			Prag1 (MGI:1196223)			
chr8	8702155	8704106	8p23.1	8p23.1		609203	CLDN23	Claudin 23	CLDN23	137075	ENSG00000253958			Cldn23 (MGI:1919158)			
chr8	8783353	8893620	8p23.1	8p23.1		605352	"MFHAS1, MASL1"	Malignant fibrous histiocytoma-amplified sequences with leucine-rich tandem repeats-1	MFHAS1	9258	ENSG00000147324		"Malignant fibrous histiocytoma, 605352 (2)"	Mfhas1 (MGI:1098644)			
chr8	9136253	9151641	8p23	8p23.1		610541	"PPP1R3B, GL"	"Protein phosphatase 1, regulatory subunit 3B"	PPP1R3B	79660	ENSG00000173281			Ppp1r3b (MGI:2177268)			
chr8	9555229	9782345	Chr.8	8p23.1		603303	TNKS	"TRF1-interacting, ankyrin-related ADP-ribose polymerase (tankyrase)"	TNKS	8658	ENSG00000173273			Tnks (MGI:1341087)			
chr8	9903387	9903471	8p23.1	8p23.1		609327	"MIR124-1, MIR124A"	Micro RNA 124-1	MIR124-1	406907							
chr8	10054223	10428890	8p23.1	8p23.1		601250	MSRA	Peptide methionine sulfoxide reductase	MSRA	4482	ENSG00000175806			Msra (MGI:106916)			
chr8	10525483	10554165	8p23.1	8p23.1		615144	"PRSS55, TSP1"	"Protease, serine, 55"	PRSS55	203074	ENSG00000184647			Prss55 (MGI:1918287)			
chr8	10606348	10655106	8p23	8p23.1		608581	RP1L1	RP1-like protein 1	RP1L1	94137	ENSG00000183638		"Occult macular dystrophy, 613587 (3), Autosomal dominant"	Rp1l1 (MGI:2384303)			
chr8	10723767	10730573	8p22	8p23.1		612202	SOX7	SRY-box 7	SOX7	83595	ENSG00000171056			Sox7 (MGI:98369)			
chr8	10764960	10839898	8p23	8p23.1		606505	PINX1	PIN2-interacting protein 1	PINX1	54984	ENSG00000254093			Pinx1 (MGI:1919650)			
chr8	11284415	11328145	8p23-p22	8p23.1		606260	"MTMR9, MTMR8"	Myotubularin-related protein 9	MTMR9	66036	ENSG00000104643			Mtmr9 (MGI:2442842)			
chr8	11330985	11332185	8p21.3	8p23.1		615199	"SLC35G5, AMAC, AMAC1L2"	"Solute carrier family 35, member G5"	SLC35G5	83650	ENSG00000177710						
chr8	11421463	11475908	8p23-p22	8p23.1		610085	"FAM167A, C8orf13"	"Family with sequence similarity 167, member A"	FAM167A	83648	ENSG00000154319			Fam167a (MGI:3606565)			
chr8	11493990	11564603	8p23-p22	8p23.1		191305	"BLK, MODY11"	BLK nonreceptor tyrosine kinase	BLK	640	ENSG00000136573		"Maturity-onset diabetes of the young, type 11, 613375 (3), Autosomal dominant"	Blk (MGI:88169)			
chr8	11676918	11760001	8p23.1-p22	8p23.1		600576	"GATA4, ASD2, VSD1, TACHD, TOF"	GATA-binding protein-4	GATA4	2626	ENSG00000136574	mutations identified in 1 TACHD family	"Atrial septal defect 2, 607941 (3), Autosomal dominant; Atrioventricular septal defect 4, 614430 (3), Autosomal dominant; ?Testicular anomalies with or without congenital heart disease, 615542 (3), Autosomal dominant; Tetralogy of Fallot, 187500 (3), Autosomal dominant; Ventricular septal defect 1, 614429 (3), Autosomal dominant"	Gata4 (MGI:95664)			
chr8	11769624	11787354	8p23.1	8p23.1		608933	"NEIL2, NEI2"	Endonuclease VIII-like 2	NEIL2	252969	ENSG00000154328			Neil2 (MGI:2686058)			
chr8	11795572	11839308	8p23.1-p22	8p23.1		184420	"FDFT1, DGPT"	Farnesyl-diphosphate farnesyltransferase 1 (squalene synthase)	FDFT1	2222	ENSG00000079459			Fdft1 (MGI:102706)			
chr8	11842523	11868149	8p22	8p23.1		116810	"CTSB, CPSB"	Cathepsin B	CTSB	1508	ENSG00000164733	13q14 by rat probe		Ctsb (MGI:88561)			
chr8	12137167	12138759	8p23.1	8p23.1		610186	"USP17L2, DUB3"	Ubiquitin specific peptidase 17-like family member 2	USP17L2	377630	ENSG00000223443						
chr8	12182103	12195435	8p23.1	8p23.1		616122	FAM86B1	"Family with sequence similarity 86, member B1"	FAM86B1	85002	ENSG00000186523						
chr8	12425400	12436405	8p23.1	8p23.1		616123	FAM86B2	"Family with sequence similarity 86, member B2"	FAM86B2	653333	ENSG00000145002						
chr8	12800000	19200000	8p22			614252	ANIB11	"Aneurysm, intracranial berry, 11"		100750328		max lod at D8S552	"Aneurysm, intracranial berry, 11, 614252 (2)"				
chr8	12800000	19200000	8p22			612030	CHDS9	"Coronary heart disease, susceptibility to, 9"		100188877		max lod at D8S1106	"{Coronary heart disease, susceptibility to, 9}, 612030 (2)"				
chr8	12800000	23500000	8p22-p21.3			612789	DFNB71	"Deafness, autosomal recessive 71"	DFNB71	100302513		max lod at D8S261	"Deafness, autosomal recessive 71, 612789 (2), Autosomal recessive"				
chr8	12800000	54600000	8p22-q11			610099	MPD3	"Myopathy, distal 3"		780920		possible locus on 12q13-q22	"Myopathy, distal 3, 610099 (2), Autosomal dominant"				
chr8	12945673	13029776	8p22	8p22		615666	"KIAA1456, TRM9L"	KIAA1456 gene	TRMT9B	57604	ENSG00000250305			6430573F11Rik (MGI:2442328)			
chr8	13083360	13604615	8p22-p21.3	8p22		604258	DLC1	Deleted in liver cancer 1	DLC1	10395	ENSG00000164741		"Colorectal cancer, somatic, 114500 (3)"	Dlc1 (MGI:1354949)			
chr8	14084834	15238282	8p22	8p22		608113	"SGCZ, ZSG1"	"Sarcoglycan, zeta"	SGCZ	137868	ENSG00000185053			Sgcz (MGI:2388820)			
chr8	15540086	15766648	8p22	8p22		601385	"TUSC3, M33, D8S1992, MRT7, MRT22"	Tumor suppressor candidate 3	TUSC3	7991	ENSG00000104723		"Mental retardation, autosomal recessive 7, 611093 (3), Autosomal recessive"	Tusc3 (MGI:1933134)			
chr8	16107877	16192790	8p22	8p22		153622	"MSR1, SCARA1, SRA"	Macrophage scavenger receptor	MSR1	4481	ENSG00000038945	~11cM distal to LPL	"Barrett esophagus/esophageal adenocarcinoma, 614266 (3)"	Msr1 (MGI:98257)			
chr8	16992824	17002164	8p22-p21.3	8p22		605558	"FGF20, RHDA2"	Fibroblast growth factor-20	FGF20	26281	ENSG00000078579	mutation identified in 1 RHDA2 family	"?Renal hypodysplasia/aplasia 2, 615721 (3), Autosomal recessive"	Fgf20 (MGI:1891346)			
chr8	17027237	17133068	8p22	8p22		610633	"MICU3, EFHA2"	Mitochondrial calcium uptake protein 3	MICU3	286097	ENSG00000155970			Micu3 (MGI:1925756)			
chr8	17221980	17246908	8p22-p21.3	8p22		604913	"CNOT7, CAF1"	"CCR4-NOT transcription complex, subunit 7"	CNOT7	29883	ENSG00000198791			Cnot7 (MGI:1298230)			
chr8	17246891	17333531	8p23-p21	8p22		609927	"VPS37A, HCRP1, SPG53"	Vacuolar protein sorting 37A	VPS37A	137492	ENSG00000155975		"Spastic paraplegia 53, autosomal recessive, 614898 (3), Autosomal recessive"	Vps37a (MGI:1261835)			
chr8	17296127	17413530	8p22	8p22		603562	MTMR7	Myotubularin-related protein 7	MTMR7	9108	ENSG00000003987			Mtmr7 (MGI:1891693)			
chr8	17494348	17570567	8p22	8p22		601872	"SLC7A2, ATRC2, HCAT2"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 2"	SLC7A2	6542	ENSG00000003989			Slc7a2 (MGI:99828)			
chr8	17576432	17643132	8p22-p21.3	8p22		604584	"PDGFRL, PDGRL, PRLTS"	Platelet-derived growth factor receptor-like	PDGFRL	5157	ENSG00000104213		"Colorectal cancer, somatic, 114500 (3); Hepatocellular cancer, somatic, 114550 (3)"	Pdgfrl (MGI:1916047)			
chr8	17864379	17909982	8p22	8p22		605776	"FGL1, HFREP1"	Fibrinogen-like 1	FGL1	2267	ENSG00000104760			Fgl1 (MGI:102795)			
chr8	17922783	18029947	8p22-p21.3	8p22		600299	"PCM1, PTC4"	Pericentriolar material 1	PCM1	5108	ENSG00000078674	fused with RET to form PTC4		Pcm1 (MGI:1277958)			
chr8	18056298	18084997	8p22-p21.3	8p22		613468	"ASAH1, AC, SMAPME"	N-acylsphingosine amidohydrolase (acid ceramidase) 1	ASAH1	427	ENSG00000104763		"Farber lipogranulomatosis, 228000 (3), Autosomal recessive; Spinal muscular atrophy with progressive myoclonic epilepsy, 159950 (3), Autosomal recessive"	Asah1 (MGI:1277124)			
chr8	18170418	18223688	8p23.1-p21.3	8p22		108345	"NAT1, AAC1"	Arylamine N-acetyltransferase-1	NAT1	9	ENSG00000171428			Nat2 (MGI:109201)			
chr8	18386584	18401218	8p23.1-p21.3	8p22		612182	"NAT2, AAC2"	Arylamine N-acetyltransferase-2	NAT2	10	ENSG00000156006	acetylation polymorphism	"[Acetylation, slow], 243400 (3), Autosomal recessive"	Nat1 (MGI:97279)			
chr8	18527302	19086908	8p22	8p22		614440	"PSD3, HCA67, EFA6R"	Pleckstrin and Sec7 domains-containing protein 3	PSD3	23362	ENSG00000156011			Psd3 (MGI:1918215)			
chr8	19200000	29000000	8p21			603013	SCZD6	"Schizophrenia susceptibility locus, chromosome 8p-related"	SCZD6	8400		?neuregulin 1	"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr8	19313442	19396217	8p22	8p21.3		614968	"SH2D4A, SH2A, PPP1R38"	SH2 domain-containing protein 4A	SH2D4A	63898	ENSG00000104611			Sh2d4a (MGI:1919531)			
chr8	19404160	19758028	8p21.3	8p21.3		616615	CSGALNACT1	Chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1	55790	ENSG00000147408			Csgalnact1 (MGI:2442354)			
chr8	19817148	19852082	8p21.3	8p21.3		611353	"INTS10, INT10"	Integrator complex subunit 10	INTS10	55174	ENSG00000104613			Ints10 (MGI:1918135)			
chr8	19939070	19967258	8p22	8p21.3		609708	"LPL, LIPD, HDLCQ11"	Lipoprotein lipase	LPL	4023	ENSG00000175445		"Combined hyperlipidemia, familial, 144250 (3), Autosomal dominant; [High density lipoprotein cholesterol level QTL 11] (3); Lipoprotein lipase deficiency, 238600 (3), Autosomal recessive"	Lpl (MGI:96820)			
chr8	20144854	20183205	8p21.3	8p21.3		193002	"SLC18A1, VMAT1, VAT1, CGAT"	"Solute carrier family 18 (vesicular monoamine), member 1"	SLC18A1	6570	ENSG00000036565			Slc18a1 (MGI:106684)			
chr8	20197192	20226851	8p21.3	8p21.3		606939	"ATP6V1B2, ATP6B2, VPP3, DOOD, ZLS2"	"ATPase, H+ transporting, lysosomal, V1 subunit B, isoform 2"	ATP6V1B2	526	ENSG00000147416		"Deafness, congenital, with onychodystrophy, autosomal dominant, 124480 (3), Autosomal dominant; Zimmermann-Laband syndrome 2, 616455 (3), Autosomal dominant"	Atp6v1b2 (MGI:109618)			
chr8	20246164	20303980	8p22	8p21.3		606551	"LZTS1, F37, FEZ1"	"Leucine zipper, putative tumor suppressor 1"	LZTS1	11178	ENSG00000061337		"Esophageal squamous cell carcinoma, 133239 (3), Autosomal dominant"	Lzts1 (MGI:2684762)			
chr8	21690402	21789295	8p21	8p21.3		601956	"GFRA2, GDNFRB"	GDNF family receptor alpha-2	GFRA2	2675	ENSG00000168546			Gfra2 (MGI:1195462)			
chr8	21908872	21913716	8p21.3	8p21.3		604997	"DOK2, P56DOK"	Docking protein 2	DOK2	9046	ENSG00000147443			Dok2 (MGI:1332623)			
chr8	21919668	22006584	8p21.3	8p21.3		606140	"XPO7, RANBP16, KIAA0745"	Exportin 7	XPO7	23039	ENSG00000130227			Xpo7 (MGI:1929705)			
chr8	22023307	22036907	8p21.3	8p21.3		608073	NPM2	"Nucleophosmin/nucleoplasmin family, member 2"	NPM2	10361	ENSG00000158806			Npm2 (MGI:1890811)			
chr8	22039707	22048808	8p21.3	8p21.3		603725	"FGF17, HH20"	Fibroblast growth factor 17	FGF17	8822	ENSG00000158815		"Hypogonadotropic hypogonadism 20 with or without anosmia, 615270 (3), Autosomal dominant"	Fgf17 (MGI:1202401)			
chr8	22048954	22082526	8p21.1	8p21.3		125305	"EPB49, DMT"	Erythrocyte membrane protein band 49 (dematin)	DMTN	2039	ENSG00000158856			Dmtn (MGI:99670)			
chr8	22106871	22110354	8p21.3	8p21.3		615791	"NUDT18, MTH3"	Nucleoside diphosphate-linked moiety X motif 18	NUDT18	79873	ENSG00000275074			Nudt18 (MGI:2385853)			
chr8	22114418	22133383	8p21.2	8p21.3		602302	"HR, AU, MUHH1, HYPT4"	"Hairless, mouse, homolog of"	HR	55806	ENSG00000168453		"Alopecia universalis, 203655 (3), Autosomal recessive; Atrichia with papular lesions, 209500 (3), Autosomal recessive; Hypotrichosis 4, 146550 (3), Autosomal dominant"	Hr (MGI:96223)			
chr8	22138013	22141950	8p21.3	8p21.3		609349	"REEP4, C8orf20"	Receptor expression-enhancing protein 4	REEP4	80346	ENSG00000168476			Reep4 (MGI:1919799)			
chr8	22146829	22156830	8p21.3	8p21.3		608302	LGI3	"Leucine-rich gene, glioma-inactivated, 3"	LGI3	203190	ENSG00000168481			Lgi3 (MGI:2182619)			
chr8	22161670	22164478	8p21	8p21.3		178620	"SFTPC, SFTP2, SMDP2"	"Surfactant, pulmonary-associated protein C (pulmonary surfactant apoprotein-2, SP-C)"	SFTPC	6440	ENSG00000168484		"Surfactant metabolism dysfunction, pulmonary, 2, 610913 (3), Autosomal dominant"	Sftpc (MGI:109517)			
chr8	22165139	22212325	8p21	8p21.3		112264	"BMP1, OI13"	Bone morphogenetic protein-1	BMP1	649	ENSG00000168487	1kb 3' to SFTP2	"Osteogenesis imperfecta, type XIII, 614856 (3), Autosomal recessive"	Bmp1 (MGI:88176)			
chr8	22244961	22245042	8p21.3	8p21.3		614112	"MIR320A, MIRN320A"	Micro RNA 320A	MIR320A	407037							
chr8	22245103	22251166	8q21	8p21.3		187280	"POLR3D, BN51T, TSBN51"	"Polymerase III, RNA, subunit D"	POLR3D	661	ENSG00000168495			Polr3d (MGI:1914315)			
chr8	22275279	22356865	8p21.3	8p21.3		610312	"PIWIL2, MILI"	PIWI-like 2	PIWIL2	55124	ENSG00000197181			Piwil2 (MGI:1930036)			
chr8	22367229	22434128	8p21.3	8p21.3		608736	"SLC39A14, ZIP14, KIAA0062, HMNDYT2"	"Solute carrier family 39 (zinc transporter), member 14"	SLC39A14	23516	ENSG00000104635		"Hypermanganesemia with dystonia 2, 617013 (3), Autosomal recessive"	Slc39a14 (MGI:2384851)			
chr8	22440969	22541465	Chr.8	8p21.3		114107	"PPP3CC, CALNA3"	"Protein phosphatase-3 (formerly 2B), catalytic subunit, gamma isoform (calcineurin A gamma)"	PPP3CC	5533	ENSG00000120910			Ppp3cc (MGI:107162)			
chr8	22544989	22575494	8p21.3	8p21.3		610795	"SORBS3, SCAM1, SH3D4"	Sorbin and SH3 domains-containing 3	SORBS3	10174	ENSG00000120896			Sorbs3 (MGI:700013)			
chr8	22578740	22598024	8p21.2	8p21.3		609722	"PDLIM2, MYSTIQUE"	PDZ and LIM domain protein 2	PDLIM2	64236	ENSG00000120913			Pdlim2 (MGI:2384850)			
chr8	22604631	22620470	8p21	8p21.3		607359	"CCAR2, DBC1, KIAA1967"	Cell division cycle and apoptosis regulator 2	CCAR2	57805	ENSG00000158941			Ccar2 (MGI:2444228)			
chr8	22620417	22669147	8p21.3	8p21.3		606396	BIN3	Bridging integrator 3	BIN3	55909	ENSG00000147439			Bin3 (MGI:1929883)			
chr8	22687660	22693301	8p23-p21	8p21.3		602419	EGR3	Early growth response 3	EGR3	1960	ENSG00000179388			Egr3 (MGI:1306780)			
chr8	22713250	22941094	8p21.2	8p21.3		612473	"PEPB4, CORK1"	Phosphatidylethanolamine-binding protein 4	PEBP4	157310	ENSG00000134020			Pebp4 (MGI:1920773)			
chr8	22987405	23020196	8p21.2	8p21.3		607352	"RHOBTB2, DBC2, KIAA0717"	Rho-related BTB domain-containing protein 2	RHOBTB2	23221	ENSG00000008853			Rhobtb2 (MGI:2180557)			
chr8	23020132	23069186	8p22-p21	8p21.3		603612	"TNFRSF10B, DR5, TRAILR2"	"Tumor necrosis factor receptor superfamily, member 10B"	TNFRSF10B	8795	ENSG00000120889		"Squamous cell carcinoma, head and neck, 275355 (3), Autosomal recessive"				
chr8	23102813	23117436	8p22-p21	8p21.3		603613	"TNFRSF10C, DCR1, TRAILR3, TRID"	"Tumor necrosis factor receptor superfamily, member 10C"	TNFRSF10C	8794							
chr8	23135587	23164029	8p21	8p21.3		603614	"TNFRSF10D, DCR2, TRAILR4"	"Tumor necrosis factor receptor superfamily, member 10D"	TNFRSF10D	8793	ENSG00000173530						
chr8	23191456	23225166	8p21	8p21.3		603611	"TNFRSF10A, DR4, TRAILR1, APO2"	"Tumor necrosis factor receptor superfamily, member 10A"	TNFRSF10A	8797	ENSG00000104689			Tnfrsf10b (MGI:1341090)			
chr8	23243636	23261999	8p21.3	8p21.3		611130	CHMP7	"CHMP family, member 7"	CHMP7	91782	ENSG00000147457			Chmp7 (MGI:1913922)			
chr8	23296896	23404208	8p21.3-p21.2	8p21.3		606663	LOXL2	Lysyl oxidase-like 2	LOXL2	4017	ENSG00000134013			Loxl2 (MGI:2137913)			
chr8	23429151	23457730	8p21.3	8p21.3		607577	"ENTPD4, LYSAL1, LAP70, KIAA0392"	Ectonucleoside triphosphate diphosphohydrolase 4	ENTPD4	9583	ENSG00000197217			"Entpd4,Entpd4b (MGI:1914714,MGI:5435040)"			
chr8	23528794	23575462	8p21	8p21.2		610387	"SLC25A37, MFRN, MFRN1"	"Solute carrier family 25 (mitochondrial iron carrier), member 37"	SLC25A37	51312	ENSG00000147454			Slc25a37 (MGI:1914962)			
chr8	23678692	23682936	8p21	8p21.2		602041	"NKX3-1, NKX3A, BAPX2"	NK3 homeo box 1	NKX3-1	4824	ENSG00000167034			Nkx3-1 (MGI:97352)			
chr8	23702450	23706597	8p21	8p21.2		611770	"NKX2-6, CSX2, CTHM"	"NK2, Drosophila, homolog of, 6"	NKX2-6	137814	ENSG00000180053		"Conotruncal heart malformations, 217095 (3); Persistent truncus arteriosus, 217095 (3)"	Nkx2-6 (MGI:97351)			
chr8	23841920	23854806	8p21-p11.2	8p21.2		601185	"STC1, STC"	Stanniocalcin 1	STC1	6781	ENSG00000159167			Stc1 (MGI:109131)			
chr8	24294039	24359017	8p12	8p21.2		606188	"ADAM28, MDCL"	A disintegrin and metalloproteinase domain 28	ADAM28	10863	ENSG00000042980			Adam28 (MGI:105988)			
chr8	24384284	24406012	8p12	8p21.2		606393	"ADAMDEC1, DECYSIN"	A disintegrin and metalloproteinase domain-like protein decysin 1	ADAMDEC1	27299	ENSG00000134028			Adamdec1 (MGI:1917650)			
chr8	24440995	24509564	8p12	8p21.2		607310	ADAM7	A disintegrin and metalloproteinase domain 7	ADAM7	8756	ENSG00000069206			Adam7 (MGI:107247)			
chr8	24913760	24919092	8p21	8p21.2		162250	"NEFM, NEF3, NFM"	"Neurofilament protein, medium polypeptide"	NEFM	4741	ENSG00000104722						
chr8	24950954	24956868	8p21	8p21.2		162280	"NEFL, CMT2E, CMT1F, CMTDIG"	"Neurofilament, light polypeptide"	NEFL	4747	ENSG00000277586		"Charcot-Marie-Tooth disease, dominant intermediate G, 617882 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 1F, 607734 (3), Autosomal recessive, Autosomal dominant; Charcot-Marie-Tooth disease, type 2E, 607684 (3), Autosomal dominant"	Nefl (MGI:97313)			
chr8	25184722	25415715	8p21.2	8p21.2		616904	DOCK5	Dedicator of cytokinesis 5	DOCK5	80005	ENSG00000147459			Dock5 (MGI:2652871)			
chr8	25419257	25425039	8p21-p11.2	8p21.2		152760	"GNRH1, LNRH, HH12"	Gonadotropin-releasing hormone-1 (luteinizing-releasing hormone)	GNRH1	2796	ENSG00000147437	mutation identified in 1 HH12 family	"?Hypogonadotropic hypogonadism 12 with or without anosmia, 614841 (3), Autosomal recessive"	Gnrh1 (MGI:95789)			
chr8	25424356	25458467	8p21.2	8p21.2		617265	"KCTD9, BTBD27"	Potassium channel tetramerization domain-containing protein 9	KCTD9	54793	ENSG00000104756			Kctd9 (MGI:2145579)			
chr8	25841729	26045123	8p21.2	8p21.2		609934	EBF2	Early B-cell factor 2	EBF2	64641	ENSG00000221818			Ebf2 (MGI:894332)			
chr8	26383006	26413128	8p21	8p21.2		605368	"BNIP3L, NIX"	BCL2/adenovirus E1B 19-kD protein-interacting protein 3-like	BNIP3L	665	ENSG00000104765			"Bnip3l,Bnip3l-ps (MGI:1332659,MGI:3642435)"			
chr8	26504679	26513966	8p21.2	8p21.2		603970	"PNMA2, MA2, MM2"	Paraneoplastic MA antigen 2	PNMA2	10687	ENSG00000240694			Pnma2 (MGI:2444129)			
chr8	26514192	26658176	8p21	8p21.2		602463	"DPYSL2, DRP2, CRMP2"	Dihydropyrimidinase-like 2	DPYSL2	1808	ENSG00000092964			Dpysl2 (MGI:1349763)			
chr8	26738112	26870993	8p21	8p21.2		104221	ADRA1C	"Adrenergic, alpha-1C-, receptor"	ADRA1A	148	ENSG00000120907	.03cM from NEFL		Adra1a (MGI:104773)			
chr8	27284885	27311318	8p21.1	8p21.2		617007	"TRIM35, MAIR, HLS5, KIAA1098"	Tripartite motif-containing protein 35	TRIM35	23087	ENSG00000104228			Trim35 (MGI:1914104)			
chr8	27311481	27459390	8p22-p11.2	8p21.2		601212	"PTK2B, FAK2, PYK2"	"Protein tyrosine kinase-2, beta (focal adhesion kinase 2)"	PTK2B	2185	ENSG00000120899			Ptk2b (MGI:104908)			
chr8	27459760	27479295	8p21	8p21.2		118502	CHRNA2	"Cholinergic receptor, nicotinic, alpha polypeptide-2"	CHRNA2	1135	ENSG00000120903		"Epilepsy, nocturnal frontal lobe, type 4, 610353 (3), Autosomal dominant"	Chrna2 (MGI:87886)			
chr8	27491001	27597558	8p21-p12	8p21.2-p21.1		132811	EPHX2	"Epoxide hydrolase 2, cytoplasmic"	EPHX2	2053	ENSG00000120915		"{Hypercholesterolemia, familial, due to LDLR defect, modifier of}, 143890 (3), Autosomal dominant"	Ephx2 (MGI:99500)			
chr8	27500000	29000000	8p21.1			240400	"GULOP, GULO"	Gulonolactone (L-) oxidase pseudogene	GULOP	2989			Scurvy (3)				
chr8	27500000	72000000	8p21.1-q13.3			611945	SPG37	Spastic paraplegia 37	SPG37	100049159		max lod at D8S601	"Spastic paraplegia 37, autosomal dominant, 611945 (2), Autosomal dominant"				
chr8	27596916	27615030	8p21-p12	8p21.1		185430	"CLU, CLI, SGP2, TRPM2"	"Clusterin (complement lysis inhibitor, SP-40,40; sulfated glycoprotein 2; testosterone-repressed prostate message-2; apolipoprotein J)"	CLU	1191	ENSG00000120885			Clu (MGI:88423)			
chr8	27633664	27736593	8p21	8p21.1		602728	"SCARA3, MSLR1, CSR"	"Scavenger receptor class A, member 3"	SCARA3	51435	ENSG00000168077			Scara3 (MGI:2444418)			
chr8	27771948	27812429	8p21.1	8p21.1		609353	ESCO2	"Establishment of cohesion 1, S. cerevisiae, homolog of, 2"	ESCO2	157570	ENSG00000171320		"Roberts syndrome, 268300 (3), Autosomal recessive; SC phocomelia syndrome, 269000 (3), Autosomal recessive"	Esco2 (MGI:1919238)			
chr8	27809620	27838094	8p21.1	8p21.1		611210	"PBK, TOPK"	PDZ-binding kinase	PBK	55872	ENSG00000168078			Pbk (MGI:1289156)			
chr8	27869881	27992851	8p21.1	8p21.1		611306	SCARA5	"Scavenger receptor class A, member 5"	SCARA5	286133	ENSG00000168079			Scara5 (MGI:1918395)			
chr8	28090230	28191152	8p21.1	8p21.1		612722	"ELP3, KAT9"	"Elongation protein 3, S. cerevisiae, homolog of"	ELP3	55140	ENSG00000134014			Elp3 (MGI:1921445)			
chr8	28316978	28343354	8p21	8p21.1		601459	"PNOC, PPNOC"	Prepronociceptin	PNOC	5368	ENSG00000168081			Pnoc (MGI:105308)			
chr8	28345584	28386459	8p21.1	8p21.1		609494	"ZNF395, PBF, HDBP2"	Zinc finger protein 395	ZNF395	55893	ENSG00000186918			Zfp395 (MGI:2682318)			
chr8	28428407	28490317	8p21.1	8p21.1		608519	"FBXO16, FBX16"	F-box only protein 16	FBXO16	157574	ENSG00000214050	?8p12		Fbxo16 (MGI:1354706)			
chr8	28494204	28574267	8p21	8p21.1		606143	FZD3	"Frizzled, Drosophila, homolog of, 3"	FZD3	7976	ENSG00000104290			Fzd3 (MGI:108476)			
chr8	28607735	28753689	8p21	8p21.1		605744	"EXTL3, EXTR1, ISDNA"	Exostosin-like 3	EXTL3	2137	ENSG00000012232		"Immunoskeletal dysplasia with neurodevelopmental abnormalities, 617425 (3), Autosomal recessive"	Extl3 (MGI:1860765)			
chr8	28767657	28890225	8p21.1	8p21.1		611352	"INTS9, INT9, RC74"	Integrator complex subunit 9	INTS9	55756	ENSG00000104299			Ints9 (MGI:1098533)			
chr8	29000000	105100000	8p12-q22			611073	AD12	Alzheimer disease 12		100188830		max lod at D8S1119	"{Alzheimer disease 12}, 611073 (2)"				
chr8	29000000	36700000	8p12			612348	THPH9	Thrombophilia due to decreased release of tissue plasminogen activator					?Thrombophilia due to decreased release of tissue plasminogen (1)				
chr8	29067277	29263384	8p12	8p12		607350	"KIF13B, GAKIN, KIAA0639"	Kinesin family member 13B	KIF13B	23303	ENSG00000197892			Kif13b (MGI:1098265)			
chr8	29333061	29350749	8p12-p11	8p12		602747	"DUSP4, MKP2, HVH2"	Dual-specificity phosphatase-4 (MAP kinase phosphatase-2)	DUSP4	1846	ENSG00000120875			Dusp4 (MGI:2442191)			
chr8	30063011	30083207	8p12	8p12		614768	"TMEM66, SARAF"	Transmembrane protein 66	SARAF	51669	ENSG00000133872			Saraf (MGI:1915137)			
chr8	30095405	30137705	8p21.2-p21.1	8p12		607338	LEPROTL1	Leptin receptor overlapping transcript-like 1	LEPROTL1	23484	ENSG00000104660			Leprotl1 (MGI:1915442)			
chr8	30131453	30148767	8p12	8p12		611940	"MBOAT4, GOAT"	Membrane-bound O-acetyltransferase domain-containing 4	MBOAT4	619373	ENSG00000177669			Mboat4 (MGI:2685017)			
chr8	30156296	30183638	8p12-p11	8p12		612963	"DCTN6, WS3, P27"	Dynactin 6	DCTN6	10671	ENSG00000104671			Dctn6 (MGI:1343154)			
chr8	30384500	30572260	8p12-p11	8p12		601558	RBPMS	RNA-binding protein gene with multiple splicing	RBPMS	11030	ENSG00000157110			Rbpms (MGI:1334446)			
chr8	30578317	30658240	8p21-p12	8p12		189964	"GTF2E2, TTD6"	"General transcription factor IIE, polypeptide 2, beta subunit, 34kD"	GTF2E2	2961	ENSG00000197265		"Trichothiodystrophy 6, nonphotosensitive, 616943 (3), Autosomal recessive"	Gtf2e2 (MGI:1915403)			
chr8	30678060	30727998	8p21.1	8p12		138300	GSR	Glutathione reductase	GSR	2936	ENSG00000104687		Hemolytic anemia due to glutathione reductase deficiency (1)	Gsr (MGI:95804)			
chr8	30729130	30767005	8p12-p11.2	8p12		602155	"UBXN8, D8S2298E, REP8"	UBX domain protein 8	UBXN8	7993	ENSG00000104691			Ubxn8 (MGI:1337129)			
chr8	30785609	30812835	8p12-p11.2	8p12		176916	PPP2CB	"Protein phosphatase-2 (formerly 2A), catalytic subunit, beta isoform"	PPP2CB	5516	ENSG00000104695	pseudogene on 16		Ppp2cb (MGI:1321161)			
chr8	30831543	30913011	Chr.8	8p12		605795	TEX15	Testis-expressed gene 15	TEX15	56154	ENSG00000133863			Tex15 (MGI:1934816)			
chr8	31033261	31175870	8p12-p11.2	8p12		604611	"RECQL2, RECQ3, WRN"	"DNA helicase, RecQ-like 2"	WRN	7486	ENSG00000165392		"Werner syndrome, 277700 (3), Autosomal recessive"	Wrn (MGI:109635)			
chr8	31639221	32771715	8p22-p11	8p12		142445	"NRG1, HGL, HRGA, ARIA"	"Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator)"	NRG1	3084	ENSG00000157168		"{?Schizophrenia, susceptibility to}, 603013 (1)"				
chr8	33308101	33473145	8p12	8p12		616931	"FUT10, FUCTX"	Fucosyltransferase 10	FUT10	84750	ENSG00000172728			Fut10 (MGI:2384748)			
chr8	33498464	33513191	8p12	8p12		614426	"TTI2, C8orf41, MRT39"	TELO2-interacting protein 2	TTI2	80185	ENSG00000129696		"Mental retardation, autosomal recessive 39, 615541 (3), Autosomal recessive"	Tti2 (MGI:2384576)			
chr8	33513474	33513577	8p12	8p12		616664	SNORD13	"Small nucleolar RNA, C/D box, 13"	SNORD13	692084							
chr8	35235456	35796549	8p12	8p12		616466	"UNC5D, UNC5H4"	"Unc5. C. elegans, homolog of, D"	UNC5D	137970	ENSG00000156687			Unc5d (MGI:2389364)			
chr8	36700000	45200000	8p11			613523	SCLL	Chromosome 8p11 myeloproliferative syndrome (stem cell leukemia/lymphoma)				translocation of FGFR1 (8p11) and various partners	"Chromosome 8p11 myeloproliferative syndrome, 613523 (4)"				
chr8	36784323	36936124	8p11.23	8p11.23		615215	"KCNU1, SLO3"	"Potassium channel, subfamily U, member 1"	KCNU1	157855	ENSG00000215262			Kcnu1 (MGI:1202300)			
chr8	37695750	37700020	8p11.23	8p11.23		617045	"ZNF703, ZEPPO1, NLZ1"	Zinc finger protein 703	ZNF703	80139	ENSG00000183779			Zfp703 (MGI:2662729)			
chr8	37736578	37757800	8p11.2	8p11.23		611605	"ERLIN2, SPFH2, C8orf2, SPG18"	Endoplasmic reticulum lipid raft-associated protein 2	ERLIN2	11160	ENSG00000147475		"Spastic paraplegia 18, autosomal recessive, 611225 (3), Autosomal recessive"	Erlin2 (MGI:2387215)			
chr8	37762545	37779767	8p11.2	8p11.23		604436	"PROSC, EPVB6D"	"Proline synthetase cotranscribed, bacteria, homolog of"	PLPBP	11212	ENSG00000147471		"Epilepsy, early-onset, vitamin B6-dependent, 617290 (3), Autosomal recessive"	Plpbp (MGI:1891207)			
chr8	37796882	37843985	8p12	8p11.23		606823	"ADGRA2, GPR124, TEM5, KIAA1531"	Adhesion G protein-coupled receptor A2	ADGRA2	25960	ENSG00000020181			Adgra2 (MGI:1925810)			
chr8	37843879	37849912	8p11.23	8p11.23		607013	"BRF2, BRFU, TFIIIB50"	BRF2 subunit of RNA polymerase III transcription initiation factor	BRF2	55290	ENSG00000104221			Brf2 (MGI:1913903)			
chr8	37858946	37899496	8p11.22	8p11.23		608737	"RAB11FIP1, RCP"	RAB11 family-interacting protein 1	RAB11FIP1	80223	ENSG00000156675			Rab11fip1 (MGI:1923017)			
chr8	37962994	37966665	8p12-p11.2	8p11.23		109691	ADRB3	"Adrenergic, beta-3-, receptor"	ADRB3	155	ENSG00000188778		"{Obesity, susceptibility to}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Adrb3 (MGI:87939)			
chr8	38030501	38060364	8p12	8p11.23		602223	"EIF4EBP1, 4EBP1"	Eukaryotic translation initiation factor-4E binding protein-1	EIF4EBP1	1978	ENSG00000187840			Eif4ebp1 (MGI:103267)			
chr8	38104964	38140079	8p11.2	8p11.23		604782	"ASH2L, ASH2L2, ASH2L1"	"ASH2, Drosophila, homolog of"	ASH2L	9070	ENSG00000129691			Ash2l (MGI:1344416)			
chr8	38142699	38151081	8p11.2	8p11.23		600617	STAR	Steroidogenic acute regulatory protein	STAR	6770	ENSG00000147465		"Lipoid adrenal hyperplasia, 201710 (3), Autosomal recessive"	Star (MGI:102760)			
chr8	38163320	38176729	8p11.23	8p11.23		607281	LSM1	LSM1 protein	LSM1	27257	ENSG00000175324			Lsm1 (MGI:1914457)			
chr8	38176587	38213300	8p11.23	8p11.23		603884	"BAG4, SODD"	Bcl2-associated athanogene 4	BAG4	9530	ENSG00000156735			Bag4 (MGI:1914634)			
chr8	38231490	38273921	8p11.23	8p11.23		615003	"DDHD2, KIAA0725, SPG54"	DDHD domain-containing protein 2	DDHD2	23259	ENSG00000085788		"Spastic paraplegia 54, autosomal recessive, 615033 (3), Autosomal recessive"	Ddhd2 (MGI:1919358)			
chr8	38261789	38269434	8p11.23	8p11.23		610626	"PLPP5, PPAPDC1B, HTPAP"	Phospholipid phosphatase 5	PLPP5	84513	ENSG00000147535			Plpp5 (MGI:1919160)			
chr8	38275041	38382271	8p12	8p11.23		607083	"NSD3, WHSC1L1"	Nuclear receptor-binding SET domain protein 3	NSD3	54904	ENSG00000147548	pseudogene on 17q21; fusion partner with NUP98 in AML	"Leukemia, acute myeloid, 601626 (3), Autosomal dominant"	Nsd3 (MGI:2142581)			
chr8	38411137	38468833	8p11.2-p11.1	8p11.23		136350	"FGFR1, FLT2, OGD, KAL2, HH2, HRTFDS, ECCL"	Fibroblast growth factor receptor-1 (fms-related tyrosine kinase-2)	FGFR1	2260	ENSG00000077782	"fused with BCR, CEP1, FOP, FIM in hematologic malignancies"	"Encephalocraniocutaneous lipomatosis, 613001 (3), Somatic mosaicism; Hartsfield syndrome, 615465 (3), Autosomal dominant; Hypogonadotropic hypogonadism 2 with or without anosmia, 147950 (3), Autosomal dominant; Jackson-Weiss syndrome, 123150 (3), Autosomal dominant; Osteoglophonic dysplasia, 166250 (3), Autosomal dominant; Pfeiffer syndrome, 101600 (3), Autosomal dominant; Trigonocephaly 1, 190440 (3), Autosomal dominant"	Fgfr1 (MGI:95522)			
chr8	38728185	38853029	8p11	8p11.22		605301	TACC1	"Transforming, acidic, coiled-coil-containing protein-1"	TACC1	6867	ENSG00000147526			Tacc1 (MGI:2443510)			
chr8	38901234	38973911	Chr.8	8p11.22		607773	"PLEKHA2, TAPP2"	"Pleckstrin homology domain-containing protein, family A, member 2"	PLEKHA2	59339	ENSG00000169499			Plekha2 (MGI:1928144)			
chr8	38974148	38988661	8p11.23	8p11.22		610700	HTRA4	HTRA serine peptidase 4	HTRA4	203100	ENSG00000169495			Htra4 (MGI:3036260)			
chr8	38988807	38997138	8p11.22	8p11.22		610081	"TM2D2, BLP1"	TM2 domain-containing protein 2	TM2D2	83877	ENSG00000169490			Tm2d2 (MGI:1916992)			
chr8	38996766	39105260	8p11.23	8p11.22		602713	"ADAM9, MDC9, MCMP, CORD9"	A disintegrin and metalloproteinase domain 9	ADAM9	8754	ENSG00000168615		"Cone-rod dystrophy 9, 612775 (3)"	Adam9 (MGI:105376)			
chr8	39743734	39838288	8p11.2	8p11.22		601533	"ADAM2, FTNB, PH30, CRYN1, CRYN2"	"A disintegrin and metalloproteinase domain 2 (fertilin, beta)"	ADAM2	2515	ENSG00000104755			Adam2 (MGI:1340894)			
chr8	39913808	39928789	8p12-p11	8p11.21		147435	"IDO1, INDO, IDO"	"Indoleamine 2,3-dioxygenase"	IDO1	3620	ENSG00000131203			Ido1 (MGI:96416)			
chr8	39934954	40016390	8p12	8p11.21		612129	"IDO2, INDOL1"	"Indoleamine 2,3-dioxygenase 2"	IDO2	169355	ENSG00000188676			Ido2 (MGI:2142489)			
chr8	40153467	40155307	8p11.2	8p11.21		607702	"TCIM, C8orf4"	Transcriptional and immune response regulator	TCIM	56892	ENSG00000176907			Tcim (MGI:1916318)			
chr8	41261956	41309470	8p12-p11.1	8p11.21		604156	"SFRP1, FRP, SARP2"	Secreted frizzled-related protein 1	SFRP1	6422	ENSG00000104332			Sfrp1 (MGI:892014)			
chr8	41529204	41545045	8p11.21	8p11.21		610611	"GINS4, SLD5"	GINS complex subunit 4	GINS4	84296	ENSG00000147536			Gins4 (MGI:1923847)			
chr8	41578187	41625000	8p11.21	8p11.21		608143	"AGPAT6, LPAATZ"	1-acylglycerol-3-phosphate O-acyltransferase 6	GPAT4	137964	ENSG00000158669			Gpat4 (MGI:2142716)			
chr8	41645176	41650817	8p11.2	8p11.21		610772	"NKX6-3, NKX6.3"	"NK6, Drosophila, homolog of"	NKX6-3	157848	ENSG00000165066						
chr8	41653224	41896761	8p11.2	8p11.21		612641	"ANK1, SPH1"	"Ankyrin-1, erythrocytic"	ANK1	286	ENSG00000029534		"Spherocytosis, type 1, 182900 (3), Autosomal dominant"	Ank1 (MGI:88024)			
chr8	41929478	42052025	8p11	8p11.21		601408	"KAT6A, MYST3, MOZ, ZNF220, MRD32"	K(lysine) acetyltransferase 6A	KAT6A	7994	ENSG00000083168		"Mental retardation, autosomal dominant 32, 616268 (3), Autosomal dominant"	Kat6a (MGI:2442415)			
chr8	42152945	42171182	8p11.2	8p11.21		610469	"AP3M2, CLA20"	"Adaptor-related protein complex 3, mu-2 subunit"	AP3M2	10947	ENSG00000070718			Ap3m2 (MGI:1929214)			
chr8	42174717	42207723	8p12	8p11.21		173370	"PLAT, TPA"	"Plasminogen activator, tissue type"	PLAT	5327	ENSG00000104368		"Hyperfibrinolysis, familial, due to increased release of PLAT, 612348 (1); Thrombophilia, familial, due to decreased release of PLAT, 612348 (1)"	Plat (MGI:97610)			
chr8	42270726	42332652	8p11.2	8p11.21		603258	"IKBKB, NFKBIKB, IMD15"	"Inhibitor of kappa light polypeptide gene enhancer in B cells, kinase of, beta"	IKBKB	3551	ENSG00000104365		"Immunodeficiency 15, 615592 (3), Autosomal recessive"	Ikbkb (MGI:1338071)			
chr8	42338451	42371812	8p11.2	8p11.21		174760	POLB	"Polymerase (DNA directed), beta"	POLB	5423	ENSG00000070501			Polb (MGI:97740)			
chr8	42373193	42391321	8p11.2-p11.1	8p11.21		605417	DKK4	"Dickkopf, Xenopus, homolog of, 4"	DKK4	27121	ENSG00000104371			Dkk4 (MGI:2385299)			
chr8	42391623	42405936	8p11.2	8p11.21		610029	VDAC3	Voltage-dependent anion channel 3	VDAC3	7419	ENSG00000078668			Vdac3 (MGI:106922)			
chr8	42416461	42542212	8p11.21	8p11.21		158378	"SLC20A2, MLVAR, GLVR2, IBGC1"	"Solute carrier family 20, phosphate transporter, member 2 (murine leukemia virus, amphotropic, receptor for)"	SLC20A2	6575	ENSG00000168575		"Basal ganglia calcification, idiopathic, 1, 213600 (3), Autosomal dominant"	Slc20a2 (MGI:97851)			
chr8	42697375	42737406	8p11.2	8p11.21		118508	CHRNB3	"Cholinergic receptor, nicotinic, beta polypeptide-3"	CHRNB3	1142	ENSG00000147432			Chrnb3 (MGI:106212)			
chr8	42752619	42768785	8p11.21	8p11.21		606888	CHRNA6	"Cholinergic receptor, neuronal nicotinic, alpha polypeptide 6"	CHRNA6	8973	ENSG00000147434			Chrna6 (MGI:106213)			
chr8	42836673	42843330	8p11.21	8p11.21		609520	"THAP1, DYT6"	THAP domain-containing protein 1	THAP1	55145	ENSG00000131931		"Dystonia 6, torsion, 602629 (3), Autosomal dominant"	Thap1 (MGI:1921004)			
chr8	42849636	42897293	8p11.2	8p11.21		614649	"RNF170, SNAX1"	RING finger protein 170	RNF170	81790	ENSG00000120925		"Ataxia, sensory, 1, autosomal dominant, 608984 (3), Autosomal dominant"	Rnf170 (MGI:1924983)			
chr8	42896889	43030538	8p11.21	8p11.21		607825	"HOOK3, HK3"	"Hook, Drosophila, homolog of, 3"	HOOK3	84376	ENSG00000168172			Hook3 (MGI:2443554)			
chr8	43056298	43085787	8p22-q11	8p11.21		134635	FNTA	"Farnesyltransferase, CAAX box, alpha"	FNTA	2339	ENSG00000168522	"related FNTAL1 on 11, FNTAL2 on 13"		Fnta (MGI:104683)			
chr8	43093505	43123179	8p11	8p11.21		615247	"POMK, SGK196, MDDGA12, MDDGC12"	Protein-O-mannose kinase	POMK	84197	ENSG00000185900	mutation in 1 MDDGC12 family has been reported	"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12, 615249 (3), Autosomal recessive; ?Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12, 616094 (3), Autosomal recessive"	Pomk (MGI:1921903)			
chr8	43140448	43202826	8p11.1	8p11.2-p11.1		610453	"HGSNAT, TMEM76, MPS3C, RP73"	Heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT	138050	ENSG00000165102		"Mucopolysaccharidosis type IIIC (Sanfilippo C), 252930 (3), Autosomal recessive; Retinitis pigmentosa 73, 616544 (3), Autosomal recessive"	Hgsnat (MGI:1196297)			
chr8	45200000	145138636	8q			600668	CCAL1	Chondrocalcinosis 1	CCAL1	882			"Chondrocalcinosis with early-onset osteoarthritis, 600668 (2), Autosomal dominant"				
chr8	45200000	145138636	8q			109640	GPB	"Glycerol phosphatase, beta-"									
chr8	45200000	145138636	8q			606789	HBFQTL4	Fetal hemoglobin quantitative trait locus 4		171515			"Fetal hemoglobin quantitative trait locus 4, 606789 (2)"				
chr8	45200000	72000000	8q11.1-q13.3			128700	PAFC	"Preauricular fistulae, congenital"		404715		between D8S532 and D8S279	"?Preauricular fistulae, congenital, 128700 (2), Autosomal dominant"				
chr8	46840885	46855784	8q11.2	8q11.1		609543	BEYLA	BEYLA gene	LINC00293	497634							
chr8	47200000	69600000	8q11.2-q13.2			609197	"GCCD3, FGD3, GCCD2"	Glucocorticoid deficiency 3		619477		between D8S285 and D8S1718	"Glucocorticoid deficiency 3, 609197 (2), Autosomal recessive"				
chr8	47260877	47736000	8q11.21	8q11.21		615384	"SPIDR, KIAA0146"	Scaffolding protein involved in DNA repair	SPIDR	23514	ENSG00000164808			Spidr (MGI:1924834)			
chr8	47736913	47738163	8p11.2-p11.1	8q11.21		116898	CEBPD	"CCAAT/enhancer-binding protein (C/EBP), delta"	CEBPD	1052	ENSG00000221869	earlier mapped to 8q11		Cebpd (MGI:103573)			
chr8	47773107	47960182	8q11	8q11.21		600899	"PRKDC, HYRC1, DNPK1, IMD26"	"Protein kinase, DNA-activated, catalytic polypeptide (hyperradiosensitivity of murine SCID mutation, complementing-1)"	PRKDC	5591	ENSG00000253729		"Immunodeficiency 26, with or without neurologic abnormalities, 615966 (3), Autosomal recessive"	Prkdc (MGI:104779)			
chr8	47960202	47978159	8q11.2	8q11.21		602638	"MCM4, NKGCD, NKCD, IMD54"	"Minichromosome maintenance deficient, S. cerevisiae, homolog of, 4"	MCM4	4173	ENSG00000104738		"Immunodeficiency 54, 609981 (3), Autosomal recessive"	Mcm4 (MGI:103199)			
chr8	47997526	48063541	8q11.21	8q11.21		603001	"UBE2V2, UEV2, DDVIT1, EDPF1, MMS2"	Ubiquitin-conjugating enzyme E2 variant 2	UBE2V2	7336	ENSG00000169139			Ube2v2 (MGI:1917870)			
chr8	48917676	48921439	8q11	8q11.21		602150	"SNAI2, SLUG, WS2D"	"snail, Drosophila, homolog of, 2 (Neural crest transcription factor SLUG)"	SNAI2	6591	ENSG00000019549		"Piebaldism, 172800 (3), Autosomal dominant; Waardenburg syndrome, type 2D, 608890 (3), Autosomal recessive"	Snai2 (MGI:1096393)			
chr8	49909725	50796655	8q11	8q11.21		608714	"SNTG1, SYN4"	"Syntrophin, gamma-1"	SNTG1	54212	ENSG00000147481	implicated in idiopathic scoliosis		Sntg1 (MGI:1918346)			
chr8	51319574	51809444	8q11	8q11.22-q11.23		615904	"PXDNL, PMR1, VPO2"	"Peroxidasin, Drosophila, homolog-like"	PXDNL	137902	ENSG00000147485						
chr8	52110831	52409878	8q11.2	8q11.23		617155	"ST18, ZNF387, KIAA0535"	Suppression of tumorigenicity 18	ST18	9705	ENSG00000147488			St18 (MGI:2446700)			
chr8	52622457	52714465	8q11	8q11.23		606837	"RB1CC1, CC1, KIAA0203"	RB1-inducible coiled-coil 1	RB1CC1	9821	ENSG00000023287		"Breast cancer, somatic, 114480 (3)"	Rb1cc1 (MGI:1341850)			
chr8	52939907	52940893	8q11.23	8q11.23		600730	"NPBWR1, GPR7"	Neuropeptides B and W receptor 1	NPBWR1	2831	ENSG00000183729	previously assigned to 10q11.2-q21.1 by FISH		Npbwr1 (MGI:891989)			
chr8	53225715	53251696	8q11.2	8q11.23		165196	OPRK1	"Opiate receptor, kappa-1"	OPRK1	4986	ENSG00000082556			Oprk1 (MGI:97439)			
chr8	53966553	54022455	8q11.23	8q11.23		601425	"TCEA1, TF2S, GTF2S"	"Transcription elongation factor A, SII, 1"	TCEA1	6917	ENSG00000187735	previously mapped to 3p22-p21.3		Tcea1 (MGI:1196624)			
chr8	54046366	54102016	Chr.8	8q11.23		605599	LYPLA1	Lysophospholipase I	LYPLA1	10434	ENSG00000120992			Lypla1 (MGI:1344588)			
chr8	54135220	54148513	8q11.2-q13	8q11.23		611828	MRPL15	Mitochondrial ribosomal protein L15	MRPL15	29088	ENSG00000137547			Mrpl15 (MGI:1351639)			
chr8	54457934	54460895	8q12-q13	8q11.23		610928	"SOX17, VUR3"	SRY-box 17	SOX17	64321	ENSG00000164736		"Vesicoureteral reflux 3, 613674 (3), Autosomal dominant"	Sox17 (MGI:107543)			
chr8	54509447	54630833	8q11-q13	8q11.2-q12.1		603937	"RP1, ORP1"	Oxygen-regulated photoreceptor protein-1 (retinitis pigmentosa-1)	RP1	6101	ENSG00000104237		"Retinitis pigmentosa 1, 180100 (3), Autosomal recessive, Autosomal dominant"	Rp1 (MGI:1341105)			
chr8	54600000	60600000	8q12.1			612587	ANIB10	"Aneurysm, intracranial berry, 10"		100271689		associated with rs10958409	"{Aneurysm, intracranial berry, 10}, 612587 (2)"				
chr8	54600000	65100000	8q12			608765	IS3	"Scoliosis, isolated, susceptibility to, 3"					"{Scoliosis, isolated, susceptibility to, 3}, 608765 (2)"				
chr8	54600000	72000000	8q12-q13			611046	MTBS2	"Mycobacterium tuberculosis, susceptibility to, 2"		100188829		max lod at D8S1723	"{Mycobacterium tuberculosis, susceptibility to, 2}, 611046 (2)"				
chr8	55773231	55826444	8q11	8q12.1		606461	"TGS1, NCOA6IP, PIMT"	"Trimethylguanosine synthase, S. cerevisiae, homolog of"	TGS1	96764	ENSG00000137574			Tgs1 (MGI:2151797)			
chr8	55876040	56012446	8q13-qter	8q12.1		165120	LYN	Yamaguchi sarcoma viral (v-yes-1) related oncogene homolog	LYN	4067	ENSG00000254087			Lyn (MGI:96892)			
chr8	56068179	56074580	8q12.1	8q12.1		603682	RPS20	Ribosomal protein S20	RPS20	6224	ENSG00000008988			Rps20 (MGI:1914677)			
chr8	56112941	56113981	8q11	8q12.1		190060	MOS	"Oncogene MOS, Moloney murine sarcoma virus"	MOS	4342	ENSG00000172680			Mos (MGI:97052)			
chr8	56160908	56211326	8q12	8q12.1		603026	"PLAG1, SGPA, PSA"	Pleomorphic adenoma gene 1	PLAG1	5324	ENSG00000181690	fused with CTNNB1 in SGPA	"Adenomas, salivary gland pleomorphic, somatic, 181030 (3)"	Plag1 (MGI:1891916)			
chr8	56211637	56218797	8q12	8q12.1		611238	CHCHD7	Coiled-coil-helix-coiled-coil-helix domain-containing protein 7	CHCHD7	79145	ENSG00000170791			Chchd7 (MGI:1913683)			
chr8	56299647	56320775	8q12.1	8q12.1		608989	RDHE2	"Retinal dehydrogenase, epidermal, 2"	SDR16C5	195814	ENSG00000170786			Sdr16c5 (MGI:2668443)			
chr8	56440953	56446733	8q23-q24	8q12.1		131330	PENK	Proenkephalin	PENK	5179	ENSG00000181195			Penk (MGI:104629)			
chr8	56957928	56993873	8q12.1	8q12.1		614010	"IMPAD1, GPAPP, IMPA3"	Inositol monophosphatase domain-containing protein 1	IMPAD1	54928	ENSG00000104331		"Chondrodysplasia with joint dislocations, GPAPP type, 614078 (3), Autosomal recessive"	Impad1 (MGI:1915720)			
chr8	57994508	58149717	8q12.1	8q12.1		611394	"FAM110B, C8orf72"	"Family with sequence similarity 110, member B"	FAM110B	90362	ENSG00000169122			Fam110b (MGI:1916593)			
chr8	58411263	58451507	8q12.1	8q12.1		610686	"UBXN2B, LOC137886, p37"	UBX domain protein 2B	UBXN2B	137886	ENSG00000215114			Ubxn2b (MGI:1915303)			
chr8	58490177	58500160	8q11-q12	8q12.1		118455	"CYP7A1, CYP7"	"Cytochrome P450, subfamily VII (cholesterol 7-alpha-monooxygenase), polypeptide 1"	CYP7A1	1581	ENSG00000167910			Cyp7a1 (MGI:106091)			
chr8	58552923	58582859	8q12.1	8q12.1		602217	"SDCBP, TACIP18, MDA9"	Syndecan-binding protein	SDCBP	6386	ENSG00000137575			Sdcbp (MGI:1337026)			
chr8	58583503	58659844	8q12-q13	8q12.1		603043	"NSMAF, FAN"	Neutral sphingomyelinase activation-associated factor	NSMAF	8439	ENSG00000035681			Nsmaf (MGI:1341864)			
chr8	58805417	59119292	8q12.1	8q12.1		606863	"TOX, KIAA0808"	"Thymus high mobility group box protein, mouse, homolog of"	TOX	9760	ENSG00000198846			Tox (MGI:2181659)			
chr8	60185419	60281422	8q11-q12	8q12.1		114815	"CA8, CALS, CARP, CAMRQ3"	Carbonic anhydrase VIII	CA8	767	ENSG00000178538		"Cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3, 613227 (3), Autosomal recessive"	Car8 (MGI:88253)			
chr8	60516909	60623643	8q12.1	8q12.1-q12.2		179509	"RAB2, RAB2A"	Ras-associated protein RAB2	RAB2A	5862	ENSG00000104388			Rab2a (MGI:1928750)			
chr8	60600000	85900000	8q12.2-q21.2			600257	"DEL8q12q21, C8DELq12q21"	Bor-Duane hydrocephalus contiguous gene syndrome (chromosome 8q12.1-q21.2 deletion syndrome)					"Bor-Duane hydrocephalus contiguous gene syndrome, 600257 (4), Autosomal dominant"				
chr8	60600000	85900000	8q12.2-q21.2			123155	HDCPH1	"Hydrocephalus, autosomal dominant"					"?Hydrocephalus, autosomal dominant, 123155 (2), Autosomal dominant"				
chr8	60678743	60868027	8q12.1	8q12.2		608892	"CHD7, HH5"	Chromodomain helicase DNA binding protein 7	CHD7	55636	ENSG00000171316		"CHARGE syndrome, 214800 (3), Autosomal dominant; Hypogonadotropic hypogonadism 5 with or without anosmia, 612370 (3), Autosomal dominant"	Chd7 (MGI:2444748)			
chr8	60964832	61501644	8q12.2	8q12.2-q12.3		611292	"CLVS1, RLBP1L1, CRALBPL"	Clavesin 1	CLVS1	157807	ENSG00000177182			Clvs1 (MGI:1921688)			
chr8	61500555	61714639	8q12.1	8q12.3		600582	"ASPH, HAAH, FDLAB"	Aspartate beta-hydroxylase (junctin; junctate)	ASPH	444	ENSG00000198363		"Traboulsi syndrome, 601552 (3), Autosomal recessive"	Asph (MGI:1914186)			
chr8	62248941	62999651	8q12.13	8q12.3		612872	NKAIN3	Na+/K+ transporting ATPase-interacting 3	NKAIN3	286183				Nkain3 (MGI:2444830)			
chr8	63015078	63039050	8q12.3	8q12.3		601509	GGH	Gamma-glutamyl hydrolase	GGH	8836	ENSG00000137563			Ggh (MGI:1329035)			
chr8	63059487	63086522	8q13.1-q13.3	8q12.3		600415	"TTPA, TTP1, AVED"	"Tocopherol, alpha, transfer protein"	TTPA	7274	ENSG00000137561		"Ataxia with isolated vitamin E deficiency, 277460 (3), Autosomal recessive"	Ttpa (MGI:1354168)			
chr8	64580237	64583633	8q13	8q12.3		613483	"BHLHE22, BHLHB5, BETA3"	"Basic helix-loop-helix family, member E22"	BHLHE22	27319	ENSG00000180828			Bhlhe22 (MGI:1930001)			
chr8	64586592	64798790	8q21.3	8q12.3		603711	"CYP7B1, CBAS3, SPG5A"	"Cytochrome P450, subfamily VIIB (oxysterol 7-alpha-hydroxylase), polypeptide 1"	CYP7B1	9420	ENSG00000172817		"Bile acid synthesis defect, congenital, 3, 613812 (3), Autosomal recessive; Spastic paraplegia 5A, autosomal recessive, 270800 (3), Autosomal recessive"	Cyp7b1 (MGI:104978)			
chr8	65100000	116700000	8q13-q23			607731	CMT2H	"Charcot-Marie-Tooth disease, axonal, type 2H"		619496		between D8S1807 and D8S548	"Charcot-Marie-Tooth disease, axonal, type 2H, 607731 (2), Autosomal recessive"				
chr8	65100000	72000000	8q13			600383	"DEL8q13, C8DELq13"	Mesomelia-synostoses syndrome (Chromosome 8q13 deletion syndrome)				contiguous gene deletion of SULF1 and SLCO5A1	"Mesomelia-synostoses syndrome, 600383 (4), Autosomal dominant"				
chr8	65100000	72000000	8q13			126800	"DURS1, DUS"	Duane retraction syndrome 1	DURS1	10674			"Duane retraction syndrome 1, 126800 (2), Autosomal dominant"				
chr8	65100000	92300000	8q13-q21			121210	1-Feb	"Febrile seizures, familial, 1"	1-Feb	2233			"Febrile seizures, familial, 1, 121210 (2), Autosomal dominant"				
chr8	65714333	65841733	8q13-q22	8q13.1		171885	"PDE7A, HCP1"	Phosphodiesterase-7A	PDE7A	5150	ENSG00000205268			Pde7a (MGI:1202402)			
chr8	66014977	66101242	8q13.1	8q13.1		613945	DNAJC5B	"DNAJ/HSP40 homolog, subfamily C, member 5, beta"	DNAJC5B	85479	ENSG00000147570			Dnajc5b (MGI:1913576)			
chr8	66112666	66175484	8q13.1	8q13.1		606469	"TRIM55, RNF29, MURF2"	Tripartite motif containing 55	TRIM55	84675	ENSG00000147573			Trim55 (MGI:3036269)			
chr8	66176376	66178644	8q13	8q13.1		122560	CRH	Corticotropin releasing hormone	CRH	1392	ENSG00000147571			Crh (MGI:88496)			
chr8	66432482	66468808	8q13.1	8q13.1		611083	"ADHFE1, HOT, ADH8"	"Alcohol dehydrogenase, iron-containing, 1"	ADHFE1	137872	ENSG00000147576			Adhfe1 (MGI:1923437)			
chr8	66562174	66613248	8q22	8q13.1		159405	MYBL1	Avian myeloblastosis viral (v-myb) oncogene homolog like-1	MYBL1	4603	ENSG00000185697			Mybl1 (MGI:99925)			
chr8	66630252	66667216	8q13	8q13.1		611745	"VCPIP1 VCIP135, KIAA1850"	VCP/p47 complex-interacting protein 1	VCPIP1	80124	ENSG00000175073			Vcpip1 (MGI:1917925)			
chr8	66712417	66862021	8q12.3-q13.1	8q13.1		607591	"SGK3, SGKL, CISK"	Serum/glucocorticoid-regulated kinase 3	SGK3	23678	ENSG00000104205			Sgk3 (MGI:2182368)			
chr8	66870748	66926435	8q13.1	8q13.1		617545	"MCMDC2, C8orf45"	Minichromosome maintenance domain-containing protein 2	MCMDC2	157777	ENSG00000178460			Mcmdc2 (MGI:3045334)			
chr8	66921689	66925540	8q13	8q13.1		612215	"SNHG6, U87HG"	Small nucleolar RNA host gene 6	SNHG6	641638							
chr8	66922473	66922548	8q13	8q13.1		612216	"SNORD87, U87"	"Small nucleolar RNA, C/D box, 87"	SNORD87	641648		within intron 2 of SNHG6					
chr8	66987675	67028550	8q13.1	8q13.1		617720	"PPP1R42, TLRR, LRRC67"	"Protein phosphatase 1, rebulatory subunit 42"	PPP1R42	286187	ENSG00000178125			Ppp1r42 (MGI:1921138)			
chr8	67043078	67062326	8q13.2	8q13.1		604850	"COPS5, JAB1, SGN5"	"COP9, subunit 5"	COPS5	10987	ENSG00000121022			Cops5 (MGI:1349415)			
chr8	67062416	67198002	8q13.2	8q13.1-q13.2		611654	"CSPP1, CSPP, JBTS21"	Centrosome spindle pole-associated protein 1	CSPP1	79848	ENSG00000104218		"Joubert syndrome 21, 615636 (3), Autosomal recessive"	Cspp1 (MGI:2681832)			
chr8	67174297	67343823	8q13	8q13.2		604141	"ARFGEF1, ARFGEP1, BIG1, P200"	ADP-ribosylation factor guanine nucleotide exchange factor 1	ARFGEF1	10565	ENSG00000066777			Arfgef1 (MGI:2442988)			
chr8	67422169	67747113	8q13	8q13.2		609562	"CPA6, CPAH, ETL5, FEB11"	Carboxypeptidase A6	CPA6	57094	ENSG00000165078		"Epilepsy, familial temporal lobe, 5, 614417 (3), Autosomal recessive, Autosomal dominant; Febrile seizures, familial, 11, 614418 (3), Autosomal recessive"	Cpa6 (MGI:3045348)			
chr8	67951917	68237032	8q13.1-q13.2	8q13.2		612139	"PREX2, DEPDC2"	"Phosphatidylinositol 3,4,5-trisphosphate-dependent RAC exchanger 2"	PREX2	80243	ENSG00000046889			Prex2 (MGI:1923385)			
chr8	69466623	69660911	8q13.3	8q13.2-q13.3		610012	"SULF1, KIAA1077"	Sulfatase 1	SULF1	23213	ENSG00000137573			Sulf1 (MGI:2138563)			
chr8	69667045	69835063	8q13.3	8q13.3		613543	"SLCO5A1, OATPRP4, SLC21A15, OATPJ, OATP5A1"	"Solute carrier organic anion transporter family, member 5A1"	SLCO5A1	81796	ENSG00000137571			Slco5a1 (MGI:2443431)			
chr8	70051612	70071326	8q13.3	8q13.3		611781	"PRDM14, PFM11"	PR domain-containing protein 14	PRDM14	63978	ENSG00000147596			Prdm14 (MGI:3588194)			
chr8	70109761	70405389	8q13.2-q13.3	8q13.3		601993	"NCOA2, GRIP1, TIF2, SRC2"	Nuclear receptor coactivator 2	NCOA2	10499	ENSG00000140396			Ncoa2 (MGI:1276533)			
chr8	70573217	70608458	Chr.8	8q13.3		605190	TRAM	Translocating chain-associating membrane protein	TRAM1	23471	ENSG00000067167			Tram1 (MGI:1919515)			
chr8	71197432	71548129	8q13.3	8q13.3		601653	"EYA1, BOR, BOS1, OFC1"	"Eyes absent, Drosophila, homolog of, 1"	EYA1	2138	ENSG00000104313	mutation identified in 1 OFC1 family	"Anterior segment anomalies with or without cataract, 602588 (3), Autosomal dominant; Branchiootic syndrome 1, 602588 (3), Autosomal dominant; Branchiootorenal syndrome 1, with or without cataracts, 113650 (3), Autosomal dominant; ?Otofaciocervical syndrome, 166780 (3), Autosomal dominant"	Eya1 (MGI:109344)			
chr8	71841541	71844495	8q13.3	8q13.3		603628	"MSC, ABF1, MYOR"	Musculin	MSC	9242	ENSG00000178860			Msc (MGI:1333884)			
chr8	72000000	74600000	8q21.11			614230	"DEL8q21.11, C8DELq21.11"	Chromosome 8q21.11 deletion syndrome				"contiguous gene deletion; minimal region (GRCh37, 8:77226464-77766239"	"Chromosome 8q21.11 deletion syndrome, 614230 (4), Autosomal dominant, Isolated cases"				
chr8	72000000	145138636	8q21.1-qter			138480	GLYB	"Glycine auxotroph B, complementation of hamster"	GLYB	2757		gly(-)B					
chr8	72000000	105100000	8q21-q22			258500	OPA6	Optic atrophy 6	OPA6	777778		between D8S1702 and D8S1794	"Optic atrophy 6, 258500 (2), Autosomal recessive"				
chr8	72021250	72094884	8q13	8q21.11		604775	"TRPA1, ANKTM1, FEPS1"	"Transient receptor potential cation channel, subfamily A, member 1 (ankyrin-like protein with transmembrane domains 1)"	TRPA1	8989	ENSG00000104321	mutation identified in 1 FEPS1 family	"?Episodic pain syndrome, familial, 1, 615040 (3), Autosomal dominant"	Trpa1 (MGI:3522699)			
chr8	72537390	72945889	Chr.8	8q21.11		607738	"KCNB2, KV2.2"	"Potassium channel, voltage-gated, shab-related subfamily, member 2"	KCNB2	9312	ENSG00000182674			Kcnb2 (MGI:99632)			
chr8	73008855	73047751	8q13	8q21.11		600951	"TERF1, TRF1"	Telomeric repeat binding factor 1	TERF1	7013	ENSG00000147601			Terf1 (MGI:109634)			
chr8	73290638	73294425	8q	8q21.11		604166	RPL7	Ribosomal protein L7	RPL7	6129	ENSG00000147604	pseudogene on chr.5		Rpl7 (MGI:98073)			
chr8	73294601	73325284	Chr.8	8q21.11		607599	RDH10	Retinol dehydrogenase 10	RDH10	157506	ENSG00000121039			Rdh10 (MGI:1924238)			
chr8	73420368	73747707	8q13-q21.1	8q21.11		605920	STAU2	"Staufen, Drosophila, homolog of, 2"	STAU2	27067	ENSG00000040341			Stau2 (MGI:1352508)			
chr8	73780096	73878909	8q13-q21.1	8q21.11		614277	"UBE2W, UBC16"	Ubiquitin-conjugating enzyme 2W	UBE2W	55284	ENSG00000104343			Ube2w (MGI:1914049)			
chr8	73945137	73972286	Chr.8	8q21.11		600788	TCEB1	"Transcription elongation factor B, polypeptide 1, 15kD (elongin C)"	ELOC	6921	ENSG00000154582			Eloc (MGI:1915173)			
chr8	73976141	73982782	8q21.11	8q21.11		612418	"TMEM70, MC5DN2"	Transmembrane protein 70	TMEM70	54968	ENSG00000175606		"Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3), Autosomal recessive"	Tmem70 (MGI:1915068)			
chr8	73991274	74099806	8q21.11	8q21.11		605243	"LY96, MD2"	Lymphocyte antigen 96	LY96	23643	ENSG00000154589			Ly96 (MGI:1341909)			
chr8	74234699	74321544	8q21	8q21.11		605266	"JPH1, JP1, CMT2K"	Junctophilin 1	JPH1	56704	ENSG00000104369	mutation identified in 1 CMT2K family	"?Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K, 607831 (3), Autosomal recessive, Autosomal dominant"	Jph1 (MGI:1891495)			
chr8	74350382	74488866	8q21.11	8q21.11		606598	"GDAP1, CMT4A, CMT2K, CMTRIA"	Ganglioside-induced differentiation-associated protein 1	GDAP1	54332	ENSG00000104381		"Charcot-Marie-Tooth disease, axonal, type 2K, 607831 (3), Autosomal recessive, Autosomal dominant; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, 607706 (3), Autosomal recessive; Charcot-Marie-Tooth disease, recessive intermediate, A, 608340 (3), Autosomal recessive; Charcot-Marie-Tooth disease, type 4A, 214400 (3), Autosomal recessive"	Gdap1 (MGI:1338002)			
chr8	74700000	83500000	8q21.13			612578	STQTL15	Stature quantitative trait locus 15		100270801		associated with rs2220456	"{Stature QTL 15}, 612578 (2)"				
chr8	74824536	74855043	8q21.13	8q21.13		607076	"PI15, P25TI"	Protease inhibitor 15	PI15	51050	ENSG00000137558			Pi15 (MGI:1934659)			
chr8	75407566	75566842	8q21	8q21.13		605966	HNF4G	Hepatocyte nuclear factor 4-gamma	HNF4G	3174	ENSG00000164749			Hnf4g (MGI:1353604)			
chr8	76681218	76867284	8q21.12	8q21.13		606940	"ZFHX4, ZFH4"	Zinc finger homeobox 4	ZFHX4	79776	ENSG00000091656		"?Ptosis, congenital, 178300 (2), Autosomal dominant"	Zfhx4 (MGI:2137668)			
chr8	76980257	77001043	8q21.1	8q21.13		170993	"PEX2, PAF1, PMP35, PBD5A, PBD5B, PXMP3"	Peroxisome biogenesis factor 2	PEX2	5828	ENSG00000164751		"Peroxisome biogenesis disorder 5A (Zellweger), 614866 (3), Autosomal recessive; Peroxisome biogenesis disorder 5B, 614867 (3), Autosomal recessive"	Pex2 (MGI:107486)			
chr8	78516100	78605266	Chr.8	8q21.13		606059	PKIA	"Protein kinase, cAMP-dependent catalytic, inhibitor alpha"	PKIA	5569	ENSG00000171033			Pkia (MGI:104747)			
chr8	78675869	78806829	8q12-q13	8q21.13		146660	IL7	Interleukin-7	IL7	3574	ENSG00000104432			Il7 (MGI:96561)			
chr8	79610813	79666174	8q21.13	8q21.13		600621	"STMN2, SCGN10, SCG10"	Stathmin-like 2	STMN2	11075	ENSG00000104435			Stmn2 (MGI:98241)			
chr8	79918859	80030270	8q21.1-q21.3	8q21.13		611990	"MRPS28, MRPS35"	Mitochondrial ribosomal protein S28	MRPS28	28957	ENSG00000147586			Mrps28 (MGI:1913480)			
chr8	80034867	80171658	8q21	8q21.13		604068	"TPD52, D52"	Tumor protein D52	TPD52	7163	ENSG00000076554			Tpd52 (MGI:107749)			
chr8	80967809	81112067	Chr.8	8q21.13		605767	PAG	Phosphoprotein associated with glycosphingolipid-enriched microdomains	PAG1	55824	ENSG00000076641			Pag1 (MGI:2443160)			
chr8	81280482	81284776	8q21.13	8q21.13		605168	"FABP5, PAFABP, EFABP"	Fatty acid-binding protein 5	FABP5	2171	ENSG00000164687			Fabp5 (MGI:101790)			
chr8	81440325	81447522	8q21.3-q22.1	8q21.13		170715	PMP2	Peripheral myelin protein-2	PMP2	5375	ENSG00000147588	not involved in CMT4A		Pmp2 (MGI:102667)			
chr8	81478496	81483237	8q21	8q21.13		600434	FABP4	"Fatty acid-binding protein-4, adipocyte"	FABP4	2167	ENSG00000170323			Fabp4 (MGI:88038)			
chr8	81656915	81686353	8q21.13-q21.3	8q21.13		602064	"IMPA1, MRT59"	Inositol(myo)-1(or 4)-monophosphatase-1	IMPA1	3612	ENSG00000133731		"Mental retardation, autosomal recessive 59, 617323 (3), Autosomal recessive"	Impa1 (MGI:1933158)			
chr8	81732452	81759514	8q21.12	8q21.13		610899	"CHMP4C, SNF7-3"	"CHMP family, member 4C"	CHMP4C	92421	ENSG00000164695			Chmp4c (MGI:1913621)			
chr8	81799582	81842325	8q21.13	8q21.13		614903	SNX16	Sorting nexin 16	SNX16	64089	ENSG00000104497			Snx16 (MGI:1921968)			
chr8	84182764	84921843	8q21.2	8q21.2		614648	RALYL	RALY-like protein	RALYL	138046	ENSG00000184672			Ralyl (MGI:1924147)			
chr8	85107087	85146079	8q21.2	8q21.2		617791	"LRRCC1, CLERK, KIAA1764"	Leucine-rich repeat- and coiled-coil domain-containing centrosomal protein 1	LRRCC1	85444	ENSG00000133739			Lrrcc1 (MGI:1918960)			
chr8	85177383	85214517	8q21.2	8q21.2		600967	E2F5	E2F transcription factor 5	E2F5	1875	ENSG00000133740			E2f5 (MGI:105091)			
chr8	85328228	85378153	8q22	8q21.2		114800	CA1	Carbonic anhydrase I	CA1	759	ENSG00000133742			Car1 (MGI:88268)			
chr8	85438826	85449039	8q22	8q21.2		114750	CA3	Carbonic anhydrase III	CA3	761	ENSG00000164879			Car3 (MGI:88270)			
chr8	85463901	85481491	8q22	8q21.2		611492	CA2	Carbonic anhydrase II	CA2	760	ENSG00000104267	"CA1, CA2 linked in monkey and mouse"	"Osteopetrosis, autosomal recessive 3, with renal tubular acidosis, 259730 (3), Autosomal recessive"	Car2 (MGI:88269)			
chr8	86213908	86230374	8q21.3	8q21.3		617256	"SLC7A13, AGT1, XAT2"	"Solute carrier family 7, member 13"	SLC7A13	157724	ENSG00000164893			Slc7a13 (MGI:1921337)			
chr8	86342659	86468353	8q21	8q21.3		602307	"WWP1, TIUL1"	WW domain-containing protein 1	WWP1	11059	ENSG00000123124			Wwp1 (MGI:1861728)			
chr8	86467054	86514347	8q21.3	8q21.3		611871	"FAM82B, RMD1"	"Family with sequence similarity 82, member B"	RMDN1	51115	ENSG00000176623			Rmdn1 (MGI:1913552)			
chr8	86514421	86561497	8q21.3	8q21.3		604207	"CPNE3, CPN3"	Copine III	CPNE3	8895	ENSG00000085719			Cpne3 (MGI:1917818)			
chr8	86573607	86743674	8q21-q22	8q21.3		605080	"CNGB3, ACHM3, ACHM1"	"Cyclic nucleotide-gated channel, beta-3"	CNGB3	54714	ENSG00000170289		"Achromatopsia 3, 262300 (3), Autosomal recessive; Macular degeneration, juvenile, 248200 (3), Autosomal recessive"	Cngb3 (MGI:1353562)			
chr8	88032008	88327487	8q21	8q21.3		602262	MMP16	Matrix metalloproteinase 16 (membrane-inserted)	MMP16	4325	ENSG00000156103			Mmp16 (MGI:1276107)			
chr8	89757746	89791063	8q21.3	8q21.3		603455	"RIPK2, CARDIAK, RIP2, RICK"	Receptor-interacting serine/threonine kinase 2	RIPK2	8767	ENSG00000104312			Ripk2 (MGI:1891456)			
chr8	89901867	89935613	8q21.3	8q21.3		604598	"OSGIN2, C8orf1"	Oxidative stress-induced growth inhibitor family member 2	OSGIN2	734	ENSG00000164823			Osgin2 (MGI:2384798)			
chr8	89933335	89984723	8q21	8q21.3		602667	"NBN, NBS1"	Nibrin	NBN	4683	ENSG00000104320		"Aplastic anemia, 609135 (3); Leukemia, acute lymphoblastic, 613065 (3); Nijmegen breakage syndrome, 251260 (3), Autosomal recessive"	Nbn (MGI:1351625)			
chr8	90001351	90053632	8q21.3	8q21.3		222745	DECR1	"2,4-dienoyl CoA reductase"	DECR1	1666	ENSG00000104325			Decr1 (MGI:1914710)			
chr8	90058607	90082880	8q21.3-q22.1	8q21.3		114050	CALB1	"Calbindin 1, 28kD"	CALB1	793	ENSG00000104327			Calb1 (MGI:88248)			
chr8	90994270	91040974	8q21.2	8q21.3		609864	TMEM55A	Transmembrane protein 55A	PIP4P2	55529	ENSG00000155099			Tmem55a (MGI:1919769)			
chr8	91070195	91087094	8q21.3	8q21.3		612021	"OTUD6B, DUBA5, IDDFSDA"	OTU domain-containing protein 6B	OTUD6B	51633	ENSG00000155100		"Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies, 617452 (3), Autosomal recessive"	Otud6b (MGI:1919451)			
chr8	91954966	92103450	8q22	8q21.3		133435	"RUNX1T1, CBFA2T1, AML1T1, ETO"	"unt-related transcription factor 1, translocated to, 1, cyclin D-related"	RUNX1T1	862	ENSG00000079102	fused with AML1 in t(8;21)		Runx1t1 (MGI:104793)			
chr8	92300000	97900000	8q22.1			151200	"DUP8q22.1, C8DUPq22.1"	Chromosome 8q22.1 duplication syndrome (Leri pleonosteosis)				duplication of 0.9-1.2 Mb on 8q22.1	"Leri pleonosteosis chromosome duplication syndrome, 151200 (4), Autosomal dominant"				
chr8	92300000	105100000	8q22			145701	HTC1	"Hypertrichosis universalis congenita, Ambras type"	HTC1	3341			"?Hypertrichosis universalis congenita, Ambras type, 145701 (2), Autosomal dominant"				
chr8	92300000	97900000	8q22.1			608156	"NMLFS, DEL8q22.1, C8DELq22.1"	Nablus mask-like facial syndrome (chromosome 8q22.1 deletion syndrome)					"Nablus mask-like facial syndrome, 608156 (4), Autosomal dominant, Isolated cases"				
chr8	93700251	93732369	8q22.1	8q22.1		617273	"FAM92A, FAM92A1"	"Family with sequence similarity 92, member A"	FAM92A	137392	ENSG00000188343			Fam92a (MGI:1915349)			
chr8	93754843	93832652	8q21.13-q22.1	8q22.1		609884	"TMEM67, MKS3, JBTS6, NPHP11"	Transmembrane protein 67 (meckelin)	TMEM67	91147	ENSG00000164953		"{Bardet-Biedl syndrome 14, modifier of}, 615991 (3), Autosomal recessive; COACH syndrome, 216360 (3), Autosomal recessive; Joubert syndrome 6, 610688 (3), Autosomal recessive; Meckel syndrome 3, 607361 (3), Autosomal recessive; Nephronophthisis 11, 613550 (3), Autosomal recessive"	Tmem67 (MGI:1923928)			
chr8	93916854	93926067	8q22.1	8q22.1		605993	"PDP1, PPM2C, PDPC"	Pyruvate dehydrogenase phosphatase catalytic subunit 1	PDP1	54704	ENSG00000164951		"Pyruvate dehydrogenase phosphatase deficiency, 608782 (3), Autosomal recessive"	Pdp1 (MGI:2685870)			
chr8	94127161	94217302	8q22.1	8q22.1		603017	"CDH17, CDH16, HPT1"	"Cadherin-17, liver-intestine"	CDH17	1015	ENSG00000079112			Cdh17 (MGI:1095414)			
chr8	94249248	94262344	8q13-q21	8q22.1		600164	GEM	GTP-binding protein overexpressed in skeletal muscle	GEM	2669	ENSG00000164949			Gem (MGI:99844)			
chr8	94371959	94475114	8q21.3-q22	8q22.1		604289	RAD54B	"RAD54, S. cerevisiae, homolog of, B"	RAD54B	25788	ENSG00000265817		"Colon cancer, somatic, 114500 (3); Lymphoma, non-Hodgkin, somatic, 605027 (3)"	Rad54b (MGI:3605986)			
chr8	94427711	94436951	8q22.1	8q22.1		616306	FSBP	Fibrinogen silencer-binding protein	FSBP	100861412	ENSG00000265817			Fsbp (MGI:5301008)			
chr8	94487776	94553517	8q22.1	8q22.1		616447	KIAA1429	KIAA1429 gene	VIRMA	25962	ENSG00000164944			Virma (MGI:1913435)			
chr8	94640998	94707465	8q22.1	8q22.1		612959	"ESRP1, RMB35A"	Epithelial splicing regulatory protein 1	ESRP1	54845	ENSG00000104413			Esrp1 (MGI:1917326)			
chr8	94719707	94793847	8q22.1	8q22.1		613895	DPY19L4	DPY19-like 4	DPY19L4	286148	ENSG00000156162			Dpy19l4 (MGI:2685869)			
chr8	94823289	94894663	8q22.1	8q22.1		611351	"INTS8, INT8"	Integrator complex subunit 8	INTS8	55656	ENSG00000164941			Ints8 (MGI:1919906)			
chr8	94880223	94896670	8q22.1	8q22.1		603775	CCNE2	Cyclin E2	CCNE2	9134	ENSG00000175305			Ccne2 (MGI:1329034)			
chr8	94895767	95118495	8q22.1	8q22.1		612392	"NDUFAF6, C8orf38"	"NADH dehydrogenase (ubiquinone) complex I, assembly factor 6"	NDUFAF6	137682	ENSG00000156170		"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufaf6 (MGI:1924197)			
chr8	94925971	94949386	8q22	8q22.1		606185	"TP53DINP1, P53DINP1"	Tumor protein p53 inducible nuclear protein 1	TP53INP1	94241	ENSG00000164938			Trp53inp1 (MGI:1926609)			
chr8	95133720	95156684	8q22.1	8q22.1		615208	"PLEKHF2, EAPF, PHAFIN2"	"Pleckstrin homology domain-containing protein, family F, member 2"	PLEKHF2	79666	ENSG00000175895			Plekhf2 (MGI:1919051)			
chr8	95244912	95270603	8q22.1	8q22.1		614477	"C8orf37, CORD16, RP64, BBS21"	Chromosome 8 open reading frame 37	C8orf37	157657	ENSG00000156172		"Bardet-Biedl syndrome 21, 617406 (3), Autosomal recessive; Cone-rod dystrophy 16, 614500 (3), Autosomal recessive; Retinitis pigmentosa 64, 614500 (3), Autosomal recessive"	2610301B20Rik (MGI:1914407)			
chr8	96142332	96160791	8q22.1	8q22.1		601147	"GDF6, MCOP4, KFS1, MCOPCB6, LCA17, SYNS4"	Growth/differentiation factor 6	GDF6	392255	ENSG00000156466		"Klippel-Feil syndrome 1, autosomal dominant, 118100 (3), Autosomal dominant; Leber congenital amaurosis 17, 615360 (3), Autosomal recessive; Microphthalmia with coloboma 6, digenic, 613703 (3), Autosomal dominant; Microphthalmia, isolated 4, 613094 (3); Multiple synostoses syndrome 4, 617898 (3), Autosomal dominant"	Gdf6 (MGI:95689)			
chr8	96226675	96235633	8q22	8q22.1		191330	"UQCRB, UQBP, QPC, MC3DN3"	Ubiquinol-cytochrome c reductase binding protein	UQCRB	7381	ENSG00000156467		"Mitochondrial complex III deficiency, nuclear type 3, 615158 (3), Autosomal recessive"	Uqcrb (MGI:1914780)			
chr8	96239397	96261612	8q22.1	8q22.1		616930	"MTERF3, MTERFD1"	"Transcription termination factor 3, mitochondrial"	MTERF3	51001	ENSG00000156469			Mterf3 (MGI:1913660)			
chr8	96261885	96334551	8q22	8q22.1		612792	"PTDSS1, PSS1, KIAA0024, LMHD"	Phosphatidylserine synthase 1	PTDSS1	9791	ENSG00000156471		"Lenz-Majewski hyperostotic dwarfism, 151050 (3), Autosomal dominant"	Ptdss1 (MGI:1276575)			
chr8	96493600	96611808	8q22-q24	8q22.1		142460	"SDC2, HSPG1"	"Syndecan 2 (heparan sulfate proteoglycan 1, cell surface-associated; fibroglycan)"	SDC2	6383	ENSG00000169439			Sdc2 (MGI:1349165)			
chr8	97273485	97277947	8q22	8q22.1		614721	"TSPYL5, KIAA1750"	TSPY-like 5	TSPYL5	85453	ENSG00000180543			Tspyl5 (MGI:2442458)			
chr8	97643971	97730259	8q22-q23	8q22.1		610323	"MTDH, AEG1, LYRIC"	Metadherin	MTDH	92140	ENSG00000147649			Mtdh (MGI:1914404)			
chr8	97775580	97852601	8q22.1	8q22.1		613296	LAPTM4B	"Lysosome-associated protein, transmembrane 4, beta"	LAPTM4B	55353	ENSG00000104341	"pseudogenes on 1q, 3q,3p, 4q, and 7q33-q35"		Laptm4b (MGI:1890494)			
chr8	97869020	98036719	8q22	8q22.1-q22.2		602108	MATN2	Matrilin 2	MATN2	4147	ENSG00000132561			Matn2 (MGI:109613)			
chr8	98041709	98045589	Chr.8	8q22.2		180467	RPL30	Ribosomal protein L30	RPL30	6156	ENSG00000156482			Rpl30 (MGI:98037)			
chr8	98102338	98117189	8q22	8q22.2		602487	"HRSP12, PSP, UK114"	Heat-responsive protein 12	RIDA	10247	ENSG00000132541			Rida (MGI:1095401)			
chr8	98117292	98159840	8q22	8q22.2		602486	"POP1, ANXD2"	"Processing of precursor 1, S. cerevisiae, homolog of"	POP1	10940	ENSG00000104356		"Anauxetic dysplasia 2, 617396 (3), Autosomal recessive"	Pop1 (MGI:1914974)			
chr8	98427021	98430796	8q22	8q22.2		602906	KCNS2	"Potassium voltage-gated channel, delayed-rectifier, subfamily S, member-2"	KCNS2	3788	ENSG00000156486			Kcns2 (MGI:1197011)			
chr8	98433047	98944328	8q22.2	8q22.2		605030	"STK3, MST2, KRS1"	Serine/threonine protein kinase 3	STK3	6788	ENSG00000104375			Stk3 (MGI:1928487)			
chr8	98944402	98952103	8q23	8q22.2		611297	OSR2	Odd-skipped-related 2	OSR2	116039	ENSG00000164920			Osr2 (MGI:1930813)			
chr8	99013084	99877585	8q22-q23	8q22.2		607817	"VPS13B, KIAA0532, COH1"	"Vacuolar protein sorting 13, yeast, homolog of, B"	VPS13B	157680	ENSG00000132549		"Cohen syndrome, 216550 (3), Autosomal recessive"	Vps13b (MGI:1916380)			
chr8	99877994	99894013	8q22-q23	8q22.2		124090	COX6C	"Cytochrome c oxidase, subunit VIc"	COX6C	1345	ENSG00000164919	pseudogene on 16p12		Gm6265 (MGI:3649160)			
chr8	99960935	100106945	8q22.2	8q22.2		615650	RGS22	Regulator of G protein signaling 22	RGS22	26166	ENSG00000132554			Rgs22 (MGI:3613651)			
chr8	100133359	100150568	8q22.3	8q22.2		609110	"FBXO43, EMI2, ERP1, FBX43"	F-box only protein 43	FBXO43	286151	ENSG00000156509			Fbxo43 (MGI:1926053)			
chr8	100150610	100154001	8p22	8q22.2		606033	"POLR2K, RPB12"	"Polymerase II, RNA, subunit K"	POLR2K	5440	ENSG00000147669			Polr2k (MGI:102725)			
chr8	100157868	100241903	8q22	8q22.2		603395	"SPAG1, CILD28"	Sperm-associated antigen-1	SPAG1	6674	ENSG00000104450		"Ciliary dyskinesia, primary, 28, 615505 (3), Autosomal recessive"	Spag1 (MGI:1349387)			
chr8	100500000	105100000	8q22.3			149000	"KTWS, KTS"	Klippel-Trenaunay-Weber syndrome		791122		translocation with 14q13	"Klippel-Trenaunay-Weber syndrome, 149000 (2), Isolated cases"				
chr8	100500000	105100000	8q22.3			613318	MMD2	Miyoshi muscular dystrophy 2		100505381		max lod at D10S2325	"Miyoshi muscular dystrophy 2, 613318 (2)"				
chr8	100702915	100722086	8q22	8q22.3		604679	"PABPC1, PAB1, PABP1, PABP"	"Polyadenylate-binding protein, cytoplasmic, 1"	PABPC1	26986	ENSG00000070756			Pabpc1 (MGI:1349722)			
chr8	100918575	100954067	8q22.3	8q22.3		601288	YWHAZ	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide"	YWHAZ	7534	ENSG00000164924	pseudogene on 2p25		Ywhaz (MGI:109484)			
chr8	101492438	101678103	8q22	8q22.3		608576	"GRHL2, TFCP2L3, DFNA28, ECTDS"	Grainyhead-like 2	GRHL2	79977	ENSG00000083307		"Deafness, autosomal dominant 28, 608641 (3), Autosomal dominant; Ectodermal dysplasia/short stature syndrome, 616029 (3), Autosomal recessive"	Grhl2 (MGI:2182543)			
chr8	101686541	102125080	8q22.2	8q22.3		606722	NCALD	"Neurocalcin, delta"	NCALD	83988	ENSG00000104490			Ncald (MGI:1196326)			
chr8	102204500	102239117	8q23.1	8q22.3		604712	"RRM2B, P53R2, PEOA5, MTDPS8A, MTDPS8B"	"Ribonucleotide reductase M2 B, TP53 inducible"	RRM2B	50484	ENSG00000048392		"Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy), 612075 (3), Autosomal recessive; Mitochondrial DNA depletion syndrome 8B (MNGIE type), 612075 (3), Autosomal recessive; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5, 613077 (3), Autosomal dominant"	Rrm2b (MGI:2155865)			
chr8	102252272	102412688	8q22.3	8q22.3		608413	"UBR5, EDD1, HYD, KIAA0896"	Ubiquitin protein ligase E3 component n-recognin 5	UBR5	51366	ENSG00000104517			Ubr5 (MGI:1918040)			
chr8	102551619	102561016	8q22	8q22.3		182878	ODF1	Outer dense fiber of sperm tails 1	ODF1	4956	ENSG00000155087			Odf1 (MGI:97424)			
chr8	102648776	102655901	8q22.2	8q22.3		601878	"KLF10, TIEG"	Kruppel-like factor 10	KLF10	7071	ENSG00000155090			Klf10 (MGI:1101353)			
chr8	102826301	102864199	8q22.3	8q22.3		607909	"AZIN1, OAZIN"	Antizyme inhibitor 1	AZIN1	51582	ENSG00000155096			Azin1 (MGI:1859169)			
chr8	103021019	103073056	8q22.3	8q22.3		603097	"ATP6V1C1, ATP6C, ATP6D"	"ATPase, H+ transporting, lysosomal, 42-kD, V1 subunit C, isoform 1"	ATP6V1C1	528	ENSG00000155097			Atp6v1c1 (MGI:1913585)			
chr8	103140692	103230304	8q22.3	8q22.3		606602	BAALC	"Brain and acute leukemia gene, cytoplasmic"	BAALC	79870	ENSG00000164929			Baalc (MGI:1928704)			
chr8	103298432	103332865	8q22.3-q23.1	8q22.3		603409	"FZD6, NDNC10"	"Frizzled, Drosophila, homolog of, 6"	FZD6	8323	ENSG00000164930		"Nail disorder, nonsyndromic congenital, 10, (claw-shaped nails), 614157 (3), Autosomal recessive"	Fzd6 (MGI:108474)			
chr8	103371514	103383004	8q22.3	8q22.3		610635	CTHRC1	Collagen triple-helix repeat-containing protein 1	CTHRC1	115908	ENSG00000164932		"Barrett esophagus/esophageal adenocarcinoma, 614266 (3)"	Cthrc1 (MGI:1915838)			
chr8	103398637	103415334	8q21.2	8q22.3		610815	"SLC25A32, MFT, RREI"	"Solute carrier family 25 (mitochondrial carrier, folate), member 32"	SLC25A32	81034	ENSG00000164933	mutation identified in 1 RREI patient	"?Exercise intolerance, riboflavin-responsive, 616839 (3), Autosomal recessive"	Slc25a32 (MGI:1917156)			
chr8	103414713	103443452	8q22.3	8q22.3		616196	"DCAF13, WDSOF1"	DDB1- and CUL4-associated factor 13	DCAF13	25879	ENSG00000164934			Dcaf13 (MGI:2684929)			
chr8	103499933	104254429	8q23	8q22.3		606630	"RIMS2, KIAA0751, RIM2, OBOE"	Regulating synaptic membrane exocytosis-2	RIMS2	9699	ENSG00000176406			Rims2 (MGI:2152972)			
chr8	104339086	104356873	8q22	8q22.3		605933	"TM7SF4, DCSTAMP, FIND"	"Transmembrane 7 superfamily, member 4"	DCSTAMP	81501	ENSG00000164935			Dcstamp (MGI:1923016)			
chr8	104379423	104467073	8q22	8q22.3		613326	"DPYS, DHP"	Dihydropyrimidinase	DPYS	1807	ENSG00000147647		"Dihydropyrimidinuria, 222748 (3), Autosomal recessive"	Dpys (MGI:1928679)			
chr8	105100000	116700000	8q23			612231	CRCS6	"Colorectal cancer, susceptibility to, 6"		100187710		associated with rs16892766	"{Colorectal cancer, susceptibility to, 6}, 612231 (2)"				
chr8	105100000	116700000	8q23			602429	GLC1D	"Glaucoma 1, open angle, D"	GLC1D	2724			"Glaucoma 1D, primary open angle, 602429 (2)"				
chr8	105100000	116700000	8q23			607053	HDLCQ2	High density lipoprotein cholesterol level QTL 2		353127			"[High density lipoprotein cholesterol level QTL 2], 607053 (2)"				
chr8	105100000	145138636	8q23-q24			140300	HT	Hashimoto thyroiditis		140805		?chr.12	"Hashimoto thyroiditis, 140300 (2), Autosomal dominant"				
chr8	105100000	116700000	8q23			612729	LBMQTL1	Lean body mass quantitative trait locus 1		100294719		associated with rs16892496 and rs7832552	"[Lean body mass QTL 1], 612729 (2)"				
chr8	105100000	145138636	8q23-q24			611376	MGS	Mungan syndrome		100126595		between D8S1830 and D8S1799	"Mungan syndrome, 611376 (2), Autosomal recessive"				
chr8	105100000	116700000	8q23			608796	MYMY3	Moyamoya disease 3	MYMY3	493818		max lod at D8S546	"Moyamoya disease 3, 608796 (2)"				
chr8	105318858	105804538	8q23	8q23.1		603693	"ZFPM2, FOG2, DIH3, SRXY9"	"Zinc finger protein, multitype 2 (friend of GATA2)"	ZFPM2	23414	ENSG00000169946		"Diaphragmatic hernia 3, 610187 (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant; 46XY sex reversal 9, 616067 (3), Autosomal dominant"	Zfpm2 (MGI:1334444)			
chr8	106270177	106752693	8q23	8q23.1		605609	OXR1	Oxidation resistance 1	OXR1	55074	ENSG00000164830	?pseudogene on chr.15		Oxr1 (MGI:2179326)			
chr8	106759482	106809072	8q23	8q23.1		609747	"ABRA, STARS"	Actin-binding RHO-activating protein	ABRA	137735	ENSG00000174429			Abra (MGI:2444891)			
chr8	107249481	107498054	8q22	8q23.1		601667	"ANGPT1, ANG1"	Angiopoietin-1	ANGPT1	284	ENSG00000154188			Angpt1 (MGI:108448)			
chr8	107899315	108083684	8q23.1	8q23.1		610575	"RSPO2, CRISTIN2"	"R-spondin family, member 2"	RSPO2	340419	ENSG00000147655			Rspo2 (MGI:1922667)			
chr8	108201742	108248733	8q22-q23	8q23.1		602210	"EIF3E, EIF3S6, INT6"	"Eukaryotic translation initiation factor 3, subunit E (oncogene INT6)"	EIF3E	3646	ENSG00000104408			Eif3e (MGI:99257)			
chr8	108443582	108489187	8q23.1	8q23.1		607722	"EMC2, KIAA0103"	ER membrane protein complex subunit 2	EMC2	9694	ENSG00000104412			Emc2 (MGI:1913986)			
chr8	108606849	108787614	8q23.2	8q23.1		613935	TMEM74	Transmembrane protein 74	TMEM74	157753	ENSG00000164841			Tmem74 (MGI:2443417)			
chr8	109085744	109119784	8q23	8q23.1		188545	TRHR	Thyrotropin-releasing hormone receptor	TRHR	7201	ENSG00000174417		"Thyrotropin-releasing hormone resistance, generalized (3)"	Trhr (MGI:98824)			
chr8	109240918	109334120	8q23	8q23.1		606109	CML66	Immunogenic tumor antigen CML66	NUDCD1	84955	ENSG00000120526			Nudcd1 (MGI:1914679)			
chr8	109362476	109537213	8q23	8q23.1-q23.2		607843	PKHD1L1	PKHD1-like 1	PKHD1L1	93035	ENSG00000205038			Pkhd1l1 (MGI:2183153)			
chr8	109539699	109565995	8q23	8q23.2		605772	"EBAG9, RCAS1, EB9"	Estrogen receptor-binding site-associated antigen 9	EBAG9	9166	ENSG00000147654			Ebag9 (MGI:1859920)			
chr8	109573977	109691790	8q23	8q23.2		611568	"GOLSYN, SYBU, KIAA1472"	Golgi-localized syntaphilin-related protein	SYBU	55638	ENSG00000147642			Sybu (MGI:2442392)			
chr8	109963644	109975846	8q22.3-q24.1	8q23.2		608164	"KCNV1, KV8.1"	"Potassium channel, voltage-gated, subfamily V, member 1"	KCNV1	27012	ENSG00000164794			Kcnv1 (MGI:1914748)			
chr8	112222927	113437498	8q23.3	8q23.3		608399	"CSMD3, KIAA1894"	Cub and Sushi multiple domains 3	CSMD3	114788	ENSG00000164796			Csmd3 (MGI:2386403)			
chr8	115408495	115669636	8q24.12	8q23.3		604386	TRPS1	Zinc finger transcription factor TRPS1	TRPS1	7227	ENSG00000104447		"Trichorhinophalangeal syndrome, type I, 190350 (3), Autosomal dominant; Trichorhinophalangeal syndrome, type III, 190351 (3), Autosomal dominant"	Trps1 (MGI:1927616)			
chr8	116644815	116755822	8q24.11	8q23.3-q24.1		603912	"EIF3H, EIF3S3"	"Eukaryotic translation initiation factor 3, subunit H"	EIF3H	8667	ENSG00000147677			Eif3h (MGI:1915385)			
chr8	116700000	145138636	8q24			612113	BMND10	Bone mineral density quantitative trait locus 10		100188883		associated with rs6469804 and rs6993813	"[Bone mineral density QTL 10], 612113 (2)"				
chr8	116700000	145138636	8q24			610649	BSZQTL3	Bone size quantitative trait locus 3		100188815			"[Bone size quantitative trait locus 3], 610649 (2)"				
chr8	116700000	145138636	8q24			611469	CRCS2	"Colorectal cancer, susceptibility to, 2"		100188841		associated with rs7014346	"{Colorectal cancer, susceptibility to, 2}, 611469 (2)"				
chr8	116700000	145138636	8q24			600131	ECA1	"Epilepsy, childhood absence, 1"	ECA1	50966			"Epilepsy, childhood absence, 1, 600131 (2), Autosomal dominant"				
chr8	116700000	145138636	8q24			600669	EIG1	"Epilepsy, idiopathic generalized, susceptibility to 1"	EGI	1957		?same as EBN2	"{Epilepsy, idiopathic generalized, susceptibility to, 1}, 600669 (2), Autosomal dominant"				
chr8	116700000	145138636	8q24			601068	"FAME1, BAFME1, MEBA"	"Epilepsy, myoclonic, adult familial, 1"	FCMTE1	50968			"Epilepsy, myoclonic, familial adult, 1, 601068 (2), Autosomal dominant"				
chr8	116700000	145138636	8q24			611100	HPC10	"Prostate cancer, hereditary, 10"		100188834		strongest assoc. with rs1447295	"{Prostate cancer, hereditary, 10}, 611100 (2)"				
chr8	116700000	145138636	8q24			167959	HPV18I1	Human papillomavirus type 18 integration site-1	HPV18I1	3260							
chr8	116700000	126300000	8q24.1			275220	THM	Tibial hemimelia		117193			"?Tibial hemimelia, 275220 (2), Autosomal recessive"				
chr8	116700000	126300000	8q24.11-q24.13			150230	"TRPS2, LGCR, LGS"	"Trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome)"				contiguous gene syndrome involving TRPS1 and EXT1	"Trichorhinophalangeal syndrome, type II, 150230 (4), Autosomal dominant"				
chr8	116845933	116874865	8q24	8q24.11		606462	"RAD21, SCC1, NXP1, KIAA0078, CDLS4"	"Rad21, S. pombe, homolog of"	RAD21	5885	ENSG00000164754		"Cornelia de Lange syndrome 4, 614701 (3), Autosomal dominant"	Rad21 (MGI:108016)			
chr8	116950272	117176713	8q24.11	8q24.11		611145	"SLC30A8, ZNT8"	"Solute carrier family 30 (zinc transporter), member 8"	SLC30A8	169026	ENSG00000164756		"{Diabetes mellitus, noninsulin-dependent, susceptibility to}, 125853 (3), Autosomal dominant"	Slc30a8 (MGI:2442682)			
chr8	117520712	117540261	8q24.11	8q24.11		610237	"MED30, TRAP25, THRAP6"	Mediator complex subunit 30	MED30	90390	ENSG00000164758			Med30 (MGI:1917040)			
chr8	117799362	118111818	8q24.11-q24.13	8q24.11		608177	EXT1	Exostosin 1	EXT1	2131	ENSG00000182197	distal to TRPS1	"Chondrosarcoma, 215300 (3), Autosomal recessive; Exostoses, multiple, type 1, 133700 (3), Autosomal dominant"	Ext1 (MGI:894663)			
chr8	118923556	118952143	8q24	8q24.12		602643	"TNFRSF11B, OPG, OCIF, PDB5"	"Tumor necrosis factor receptor superfamily, member 11B (osteoprotegerin)"	TNFRSF11B	4982	ENSG00000164761		"Paget disease of bone 5, juvenile-onset, 239000 (3), Autosomal recessive"	Tnfrsf11b (MGI:109587)			
chr8	118952166	119108454	8q23-q24.1	8q24.12		607620	"COLEC10, CLL1, 3MC3"	Collectin 10	COLEC10	10584	ENSG00000184374		"3MC syndrome 3, 248340 (3), Autosomal recessive"	Colec10 (MGI:3606482)			
chr8	119416311	119424437	8q24.1	8q24.12		164958	NOV	Nephroblastoma overexpressed gene	NOV	4856	ENSG00000136999	proximal to MYC		Nov (MGI:109185)			
chr8	119557076	119673575	8q24.1	8q24.12		601060	"ENPP2, PDNP2"	Ectonucleotide pyrophosphatase/phosphodiesterase 2	ENPP2	5168	ENSG00000136960			Enpp2 (MGI:1321390)			
chr8	119730772	119832857	8q24.12	8q24.12		604912	"TAF2, TAF2B, TAFII150, CIF150, MRT40"	"TAF2 RAN polymerase II, TATA box-binding protein-associated factor, 150kD"	TAF2	6873	ENSG00000064313		"Mental retardation, autosomal recessive 40, 615599 (3), Autosomal recessive"	Taf2 (MGI:2443028)			
chr8	119833940	119855929	8q24.12	8q24.12		613203	"DSCC1, DCC1"	"Defective in sister chromatid cohesion 1, S. cerevisiae, homolog of"	DSCC1	79075	ENSG00000136982			Dscc1 (MGI:1919357)			
chr8	119873654	120056201	8q24.12	8q24.12		612974	"DEPDC6, DEPTOR"	DEP domain-containing protein 6	DEPTOR	64798	ENSG00000155792			Deptor (MGI:2146322)			
chr8	120124466	120373574	8q23	8q24.12		120324	"COL14A1, UND"	"Collagen, type XIV, alpha-1 (undulin)"	COL14A1	7373	ENSG00000187955			Col14a1 (MGI:1341272)			
chr8	120395843	120445406	8q24.12	8q24.12		610200	"MRPL13, RPML13, L13A"	Mitochondrial ribosomal protein L13	MRPL13	28998	ENSG00000172172			Mrpl13 (MGI:2137218)			
chr8	120445397	120523634	8q24.1-q24.3	8q24.12		605927	MTBP	"Mouse double minute 2 homolog, binding protein of"	MTBP	27085	ENSG00000172167			Mtbp (MGI:2146005)			
chr8	120535744	120812068	8q23-q24	8q24.12		600026	"SNT2B1, A1B, SNTB1"	"Syntrophin, beta 1 (dystrophin-associated protein A1, 59kD, basic basic component 1)"	SNTB1	6641	ENSG00000172164			Sntb1 (MGI:101781)			
chr8	121500000	135400000	8q24.13-q24.22			612448	ARHI1	Age-related hearing impairment 1		100233147		between rs3765212 and rs4601326	"{Age-related hearing impairment 1}, 612448 (2)"				
chr8	121500000	130400000	8q24.13-q24.21			614936	PPKP1B	"Keratoderma, palmoplantar, punctate type IB"		101154752		between D8S1804 and D8S1720	"Keratoderma, palmoplantar, punctate type IB, 614936 (2), Autosomal dominant"				
chr8	121613030	121641389	8q24.12	8q24.13		601636	HAS2	Hyaluronan synthase-2	HAS2	3037	ENSG00000170961			Has2 (MGI:107821)			
chr8	121639345	121645324	8q24.13	8q24.13		614353	"HAS2AS1, HASNT"	HAS2 antisense RNA 1	HAS2-AS1	594842							
chr8	123013163	123042422	8q24.13	8q24.13		608813	"DERL1, DER1"	"DER1-like domain family, member 1"	DERL1	79139	ENSG00000136986			Derl1 (MGI:1915069)			
chr8	123248449	123275540	8q	8q24.13		604764	ZHX1	Zinc finger and homeodomain protein 1	ZHX1	11244	ENSG00000165156			Zhx1 (MGI:109271)			
chr8	123319849	123396464	8q24.13	8q24.13		611941	"ATAD2, ANCCA"	"ATPase family, AAA domain-containing, member 2"	ATAD2	29028	ENSG00000156802			Atad2 (MGI:1917722)			
chr8	123497886	123541252	8q24.13	8q24.13		606604	"FBXO32, MAFBX, FLJ32424, ATROGIN1"	F-box only protein 32	FBXO32	114907	ENSG00000156804			Fbxo32 (MGI:1914981)			
chr8	123680793	123737425	8q24.1-q24.2	8q24.13		602573	"ANX13, ISA"	Annexin XIII	ANXA13	312	ENSG00000104537			Anxa13 (MGI:1917037)			
chr8	124306188	124372698	8q24.13	8q24.13		616609	TMEM65	Transmembrane protein 65	TMEM65	157378	ENSG00000164983			Tmem65 (MGI:1922118)			
chr8	124450806	124453025	8q24.13	8q24.13		611244	"TRMT12, TRM12"	"tRNA methyltransferase 12, S. cerevisiae, homolog of"	TRMT12	55039	ENSG00000183665			Trmt12 (MGI:1915510)			
chr8	124474766	124488617	8q24.1	8q24.13		603046	"RNF139, TRC8, RCA1"	RING finger protein 139	RNF139	11236	ENSG00000170881		"Renal cell carcinoma, 144700 (3)"	Rnf139 (MGI:1923091)			
chr8	124539101	124549985	8q13.3	8q24.13		601445	"NDUFB9, UQOR22"	"NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9 (22kD, B22)"	NDUFB9	4715	ENSG00000147684	mutation identified in 1 family	"?Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufb9 (MGI:1913468)			
chr8	124550769	124728506	8q24.1	8q24.13		608486	"MTSS1, MIM, KIAA0429"	Metastasis suppressor 1	MTSS1	9788	ENSG00000170873			Mtss1 (MGI:2384818)			
chr8	124998477	125022282	8q24.1	8q24.13		602019	SQLE	Squalene epoxidase	SQLE	6713	ENSG00000104549			Sqle (MGI:109296)			
chr8	125024259	125091818	8q24.13	8q24.13		610657	"WSHC5, KIAA0196, SPG8, RTSC1"	"WASH complex, subunit 5"	WASHC5	9897	ENSG00000164961		"Ritscher-Schinzel syndrome 1, 220210 (3), Autosomal recessive; Spastic paraplegia 8, autosomal dominant, 603563 (3), Autosomal dominant"	Washc5 (MGI:2146110)			
chr8	125091778	125367124	8q24.13	8q24.13		617246	"NSMCE2, NSE2, MMS21"	"Non-SMC element 2, S. cerevisiae, homolog of"	NSMCE2	286053	ENSG00000156831		"Seckel syndrome 10, 617253 (3), Autosomal recessive"	Nsmce2 (MGI:1915751)			
chr8	125430289	125438404	8q24.13	8q24.13		609461	"TRIB1, TRB1, SKIP1, C8FW"	"Tribbles, Drosophila, homolog of, 1"	TRIB1	10221	ENSG00000173334			Trib1 (MGI:2443397)			
chr8	126300000	130400000	8q24.21			613032	GLM7	Glioma susceptibility 7		101409265		associated with rs55705857	"{Glioma susceptibility 7}, 613032 (2)"				
chr8	126552437	126558497	8q24.21	8q24.21		609483	"FAM84B, BCMP101"	"Family with sequence similarity 84, member B"	FAM84B	157638	ENSG00000168672			Fam84b (MGI:3026924)			
chr8	127013153	127021013	8q24	8q24.21		616043	PCAT1	"Prostate cancer-associated transcript 1, noncoding"	PCAT1	100750225							
chr8	127072693	127082220	8q24.21	8q24.21		617678	"PCAT2, PCA2, CARLO4"	"Prostate cancer-associated transcript 2, noncoding"	PCAT2	103164619							
chr8	127079873	127092594	8q24	8q24.21		615452	"PRNCR1, PCAT8"	Prostate cancer-associated noncoding RNA 1	PRNCR1	101867536							
chr8	127187784	127197626	8q24.21	8q24.21		617703	"CASC19, LINC01245, CARLO6"	"Cancer susceptibility candidate 19, noncoding"	CASC19	103021165							
chr8	127207381	127219267	8q24.21	8q24.21		617705	"CCAT1, CARLO5"	"Colon cancer-associated transcript 1, noncoding"	CCAT1	100507056							
chr8	127244636	127392630	8q24.21	8q24.21		617702	"CASC21, LINC01244, CARLO2"	"Cancer susceptibility candidate 21, noncoding"	CASC21	103021164							
chr8	127289675	127482138	8q24.21	8q24.21		617701	"CASC8, LINC00860, CARLO1"	"Cancer susceptibility candidate 8, noncoding"	CASC8	727677							
chr8	127415611	127417209	8q24.21	8q24.21		615739	"POU5F1B, POU5F1P1, OCT4PG1"	"POU domain, class 5, transcription factor 1B"	POU5F1B	5462	ENSG00000212993						
chr8	127700607	127733966	8q24.21	8q24.21		617704	"CASC11, LINC00990, CARLO7"	"Cancer susceptibility candidate 11, noncoding"	CASC11	100270680							
chr8	127735433	127742950	8q24.12-q24.13	8q24.21		190080	MYC	Avian myelocytomatosis viral (v-myc) oncogene homolog	MYC	4609	ENSG00000136997	cen-5'-3'-ter	"Burkitt lymphoma, 113970 (3), Isolated cases"	Myc (MGI:97250)			
chr8	127794532	128101252	8q24	8q24.21		165140	PVT1	Oncogene PVT-1 (MYC activator)	PVT1	5820							
chr8	129351693	129680238	8q24.21	8q24.21		613040	"CCD26, RAM"	Coiled-coil domain-containing protein 26	CCDC26	137196							
chr8	129705902	129786887	8q24.1-q24.2	8q24.21		608384	"GSDMC, MLZE"	Gasdermin C	GSDMC	56169	ENSG00000147697			"Gsdmc,Gsdmc4,Gsdmc3,Gsdmc2 (MGI:1933176,MGI:3580656,MGI:1921798,MGI:2146102)"			
chr8	130052103	130443847	8q24.1-q24.2	8q24.21-q24.22		605953	"ASAP1, DDEF1"	"Arf GTPase-activating protein with SH3 domain, ankyrin repeat, and PH domain 1"	ASAP1	50807	ENSG00000153317			Asap1 (MGI:1342335)			
chr8	130780299	131041603	8q24.2	8q24.22		103070	"ADCY8, ADCY3"	"Adenylyl cyclase-8, brain"	ADCY8	114	ENSG00000155897			Adcy8 (MGI:1341110)			
chr8	131904087	132013641	8q24.2	8q24.22		611798	"EFR3A, KIAA0143"	"EFR3, S. cerevisiae, homolog of, A"	EFR3A	23167	ENSG00000132294			Efr3a (MGI:1923990)			
chr8	132024219	132059379	8q24	8q24.22		601658	"OC90, PLA2L"	Otoconin 90 (phospholipase A2-like)	OC90	729330	ENSG00000253117	PLA2L = fusion between HHLA1 and OC90		Oc90 (MGI:1313269)			
chr8	132061485	132105264	8q24	8q24.22		604109	HHLA1	Human endogenous retrovirus-H long terminal repeat-associating 1	HHLA1	10086	ENSG00000132297			Hhla1 (MGI:3615329)			
chr8	132120857	132480756	8q24	8q24.22		602232	"KCNQ3, EBN2, BFNC2"	"Potassium voltage-gated channel, KQT-like subfamily, member 3"	KCNQ3	3786	ENSG00000184156		"Seizures, benign neonatal, 2, 121201 (3), Autosomal dominant"	Kcnq3 (MGI:1336181)			
chr8	132570418	132685038	8q24.22	8q24.22		614930	"LRRC6, LRTP, CILD19"	Leucine-rich repeat-containing protein 6	LRRC6	23639	ENSG00000129295		"Ciliary dyskinesia, primary, 19, 614935 (3), Autosomal recessive"	Lrrc6 (MGI:1859553)			
chr8	132866942	133134901	8q24.2-q24.3	8q24.22		188450	"TG, AITD3, TDH3"	Thyroglobulin	TG	7038	ENSG00000042832	distal to MYC	"{Autoimmune thyroid disease, susceptibility to, 3}, 608175 (3); Thyroid dyshormonogenesis 3, 274700 (3), Autosomal recessive"	Tg (MGI:98733)			
chr8	133036727	133103065	8q24.2-q24.3	8q24.22		601099	SLA	Src-like-adaptor	SLA	6503	ENSG00000155926	in intron of TG		Sla (MGI:104295)			
chr8	133054958	133057766	8q24	8q24.22		617440	"PTCSC1, NCRNA00197"	Papillary thyroid carcinoma susceptibility candidate 1 gene	PTCSC1	100302522							
chr8	133190906	133231689	8q24.1-q24.3	8q24.22		603398	WISP1	Wnt-1 inducible signaling pathway protein 1	WISP1	8840	ENSG00000104415			Wisp1 (MGI:1197008)			
chr8	133237170	133297586	8q24.3	8q24.22		605262	"NDRG1, HMSNL, CMT4D"	N-myc downstream-regulated gene 1	NDRG1	10397	ENSG00000104419		"Charcot-Marie-Tooth disease, type 4D, 601455 (3), Autosomal recessive"	Ndrg1 (MGI:1341799)			
chr8	134477787	134713048	8q23-q24	8q24.22		610931	"ZFAT1, ZNF406, AITD3"	Zinc finger gene in autoimmune thyroid disease 1	ZFAT	57623	ENSG00000066827		"{Autoimmune thyroid disease, susceptibility to, 3}, 608175 (3)"	Zfat (MGI:2681865)			
chr8	135457460	135656515	8q24.2	8q24.23		610421	"KHDRBS3, TSTAR, SALP, SLM2, ETOILE"	"KH domain-containing, RNA-binding, signal transduction-associated protein 3"	KHDRBS3	10656	ENSG00000131773			Khdrbs3 (MGI:1313312)			
chr8	138588234	138914086	8q24.2	8q24.2-q24.3		610026	COL22A1	"Collagen, type XXII, alpha-1 polypeptide"	COL22A1	169044	ENSG00000169436			Col22a1 (MGI:1916950)			
chr8	138900000	145138636	8q24.3			616992	"C8orf17, MOST1"	Chromosome 8 open reading frame 17	C8orf17	100507249							
chr8	138900000	145138636	8q24.3			612858	OFC12	Orofacial cleft 12		100302515		associated with rs987525	"Orofacial cleft 12, 612858 (2)"				
chr8	139600837	139703134	8q24.1-q24.3	8q24.3		605874	"KCNK9, TASK3"	"Potassium channel, subfamily K, member 9"	KCNK9	51305	ENSG00000169427		"Birk-Barel mental retardation dysmorphism syndrome, 612292 (3)"	Kcnk9 (MGI:3521816)			
chr8	139727724	140458578	8q24.3	8q24.3		611966	"TRAPPC9, NIBP, KIAA1882, MRT13"	Trafficking protein particle complex 9	TRAPPC9	83696	ENSG00000167632		"Mental retardation, autosomal recessive 13, 613192 (3), Autosomal recessive"	Trappc9 (MGI:1923760)			
chr8	140511297	140517152	8q11-q12	8q24.3		607268	"CHARC1, CHARC15, YCL1"	"Chromatin accessibility complex, subunit 1"	CHRAC1	54108	ENSG00000104472			Chrac1 (MGI:2135796)			
chr8	140520150	140642405	8q24	8q24.3		606229	"AGO2, EIF2C2"	"Argonaute 2, RISC catalytic component"	AGO2	27161	ENSG00000123908			Ago2 (MGI:2446632)			
chr8	140658381	141002078	8q24-qter	8q24.3		600758	"PTK2, FADK"	PTK2 protein tyrosine kinase	PTK2	5747	ENSG00000169398			Ptk2 (MGI:95481)			
chr8	141128561	141195803	8q24.3	8q24.3		617503	"DENND3, KIAA0870"	DENN domain-containing protein 3	DENND3	22898	ENSG00000105339			Dennd3 (MGI:2146009)			
chr8	141356484	141367264	8q24.2-q24.3	8q24.3		601908	GPR20	G protein-coupled receptor-20	GPR20	2843	ENSG00000204882			Gpr20 (MGI:2441803)			
chr8	141391994	141432453	8q24.3	8q24.3		606449	"PTP4A3, PRL3"	"Protein-tyrosine phosphatase, type 4A, 3"	PTP4A3	11156	ENSG00000184489			Ptp4a3 (MGI:1277098)			
chr8	142449702	142545008	8q24	8q24.3		602682	"ADGRB1, BAI1, GDAIF"	Adhesion G protein-coupled receptor B1	ADGRB1	575	ENSG00000181790			Adgrb1 (MGI:1933736)			
chr8	142611043	142614471	8q24	8q24.3		612461	"ARC, KIAA0278"	Activity-regulated cytoskeleton-associated protein	ARC	23237	ENSG00000198576			Arc (MGI:88067)			
chr8	142651500	142669993	8q24	8q24.3		603210	"JRK, JH8"	"Jerky, mouse, homolog of"	JRK	8629	ENSG00000234616			Jrk (MGI:106214)			
chr8	142670307	142682726	8q24.2	8q24.3		602470	PSCA	Prostate stem cell antigen	PSCA	8000	ENSG00000167653			Psca (MGI:1919623)			
chr8	142700080	142704169	8q24.3	8q24.3		615093	LY6K	"Lymphocyte antigen 6 complex, locus K"	LY6K	54742	ENSG00000160886						
chr8	142740943	142742410	8qter	8q24.3		606119	"SLURP1, MDM"	Secreted LY6/uPAR-related protein 1	SLURP1	57152	ENSG00000126233		"Meleda disease, 248300 (3), Autosomal recessive"	Slurp1 (MGI:1930923)			
chr8	142771196	142777847	Chr.8	8q24.3		606110	LYNX1	"Lynx1, mouse, homolog of"	LYNX1	66004	ENSG00000180155			Lynx1 (MGI:1345180)			
chr8	142784881	142786591	8q24-qter	8q24.3		606204	"LY6D, E48"	"Lymphocyte antigen 6 complex, locus D"	LY6D	8581	ENSG00000167656	?pseudogene ono 15q22		Ly6d (MGI:96881)			
chr8	142834800	142846845	8q24.3	8q24.3		602370	GML	Glycosylphosphatidylinositol-anchored molecule-like protein	GML	2765	ENSG00000104499			"Gml,Gml2 (MGI:1341831,MGI:3644767)"			
chr8	142872356	142879819	8q21	8q24.3		610613	"CYP11B1, P450C11, FHI"	"Cytochrome P450, subfamily XIB, polypeptide 1 (11-beta-hydroxylase; corticosteroid methyl-oxidase II (CMO II))"	CYP11B1	1584	ENSG00000160882	chimeric CYP11B1/CYP11B2 gene = anti-Lepore-like	"Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, 202010 (3), Autosomal recessive; Aldosteronism, glucocorticoid-remediable, 103900 (3), Autosomal dominant"	Cyp11b2 (MGI:88584)			
chr8	142910558	142917842	8q21	8q24.3		124080	CYP11B2	"Cytochrome P450, subfamily XIB, polypeptide 2"	CYP11B2	1585	ENSG00000179142		"Aldosterone to renin ratio raised (3); Hypoaldosteronism, congenital, due to CMO I deficiency, 203400 (3), Autosomal recessive; Hypoaldosteronism, congenital, due to CMO II deficiency, 610600 (3), Autosomal recessive; {Low renin hypertension, susceptibility to} (3)"	Cyp11b1 (MGI:88583)			
chr8	143018484	143022409	8q24.3	8q24.3		601384	"LY6E, RIGE, SCA2"	"Lymphocyte antigen 6 complex, locus E (retinoic acid induced gene E)"	LY6E	4061	ENSG00000160932			Ly6e (MGI:106651)			
chr8	143157913	143160635	8q24.3	8q24.3		603625	LY6H	"Lymphocyte antigen 6 complex, locus H"	LY6H	4062	ENSG00000176956			Ly6h (MGI:1346030)			
chr8	143213192	143217169	8q24.3	8q24.3		612757	"GPIHBP1, HYPL1D"	Glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1	GPIHBP1	338328	ENSG00000277494		"Hyperlipoproteinemia, type 1D, 615947 (3), Autosomal recessive"				
chr8	143267436	143276930	8q24.3	8q24.3		165280	"GLI4, HKR4"	GLI-Kruppel family member GLI4 (oncogene HKR4)	GLI4	2738	ENSG00000250571						
chr8	143309323	143359976	8q24.3	8q24.3		606387	TOP1MT	"Topoisomerase I, mitochondrial"	TOP1MT	116447	ENSG00000184428			Top1mt (MGI:1920210)			
chr8	143368826	143384219	8q24.3	8q24.3		601031	"RHPN1, ODF5"	Rhophilin 1	RHPN1	114822	ENSG00000158106			Rhpn1 (MGI:1098783)			
chr8	143428059	143430431	8q24	8q24.3		610303	"MAFA, RIPE3B1, INSDM"	v-MAF avian musculoaponeurotic fibrosarcoma oncogene homolog A	MAFA	389692	ENSG00000182759		"Insulinomatosis and diabetes mellitus, 147630 (3), Autosomal dominant"	Mafa (MGI:2673307)			
chr8	143553386	143563061	8q24.3	8q24.3		617042	"GSDMD, GSDMDC1, DFNA5L"	Gasdermin D	GSDMD	79792	ENSG00000104518			Gsdmd (MGI:1916396)			
chr8	143574584	143578350	8q24.3	8q24.3		611552	NAPRT1	Nicotinate phosphoribosyltransferase domain-containing 1	NAPRT	93100	ENSG00000147813			Naprt (MGI:2442664)			
chr8	143579721	143597674	8q24.3	8q24.3		130592	"EEF1D, EF1D"	"Eukaryotic translation elongation factor 1, delta"	EEF1D	1936	ENSG00000104529			Eef1d (MGI:1913906)			
chr8	143603223	143609613	8q24.3	8q24.3		616408	"PYCRL, PYCR3"	Pyrroline-5-carboxylate reductase-like	PYCR3	65263	ENSG00000104524			Pycrl (MGI:1913444)			
chr8	143612617	143618042	8q24.3	8q24.3		137020	TSTA3	Tissue-specific transplantation antigen-3	TSTA3	7264	ENSG00000104522			Tsta3 (MGI:98857)			
chr8	143723932	143741625	8q24.3	8q24.3		611927	"FAM83H, AI3A"	"Family with sequence similarity 83, member H"	FAM83H	286077	ENSG00000180921		"Amelogenesis imperfecta, type IIIA, 130900 (3), Autosomal dominant"	Fam83h (MGI:2145900)			
chr8	143790919	143815378	8q24.3	8q24.3		607733	"SCRIB, SCRB1, KIAA0147"	"Scribble, Drosophila, homolog of"	SCRIB	23513	ENSG00000180900			Scrib (MGI:2145950)			
chr8	143816343	143830040	8q24.3	8q24.3		604819	"PUF60, FIR, SIAHBP1, VRJS"	"Poly-U-binding splicing factor, 60kD"	PUF60	22827	ENSG00000179950		"Verheij syndrome, 615583 (3), Autosomal dominant"	Puf60 (MGI:1915209)			
chr8	143829775	143840973	8q24.3	8q24.3		615563	NRBP2	Nuclear receptor-binding protein 2	NRBP2	340371	ENSG00000185189						
chr8	143857318	143879042	8q24.3	8q24.3		607553	EPPK1	Epiplakin 1	EPPK1	83481	ENSG00000261150			Eppk1 (MGI:2386306)			
chr8	143915146	143976799	8q24	8q24.3		601282	"PLEC1, PLEC, PLTN, EBS1, LGMD2Q, EBSOG, EBSPA, EBSMD, EBSND"	Plectin 1	PLEC	5339	ENSG00000178209	mutation identified in 1 EBSND family	"Epidermolysis bullosa simplex with muscular dystrophy, 226670 (3), Autosomal recessive; ?Epidermolysis bullosa simplex with nail dystrophy, 616487 (3), Autosomal recessive; Epidermolysis bullosa simplex with pyloric atresia, 612138 (3), Autosomal recessive; Epidermolysis bullosa simplex, Ogna type, 131950 (3), Autosomal dominant; Muscular dystrophy, limb-girdle, type 2Q, 613723 (3), Autosomal recessive"	Plec (MGI:1277961)			
chr8	143945190	143945278	8q24.3	8q24.3		613716	"MIR661, MIRN661"	Micro RNA 661	MIR661	724031							
chr8	143990057	143993414	8q24.3	8q24.3		138251	"GRINA, NMDARA1"	"Glutamate receptor, ionotropic, N-methyl"	GRINA	2907	ENSG00000178719			Grina (MGI:1913418)			
chr8	144010991	144047113	8q24	8q24.3		610874	SPATC1	Spermatogenesis- and centriole-associated 1 (speriolin)	SPATC1	375686	ENSG00000186583			Spatc1 (MGI:1921531)			
chr8	144051265	144064025	8q24.3	8q24.3		614243	"OPLAH, OPLAHD"	5-oxoprolinase (ATP-hydrolyzing)	OPLAH	26873	ENSG00000178814		"5-oxoprolinase deficiency, 260005 (3), Autosomal recessive, Autosomal dominant"	Oplah (MGI:1922725)			
chr8	144064060	144080647	8q24.3	8q24.3		606491	"EXOSC4, RRP41"	Exosome component 4	EXOSC4	54512	ENSG00000178896			Exosc4 (MGI:1923576)			
chr8	144082620	144086215	8q24	8q24.3		603048	"GPAA1, GAA1, GPIBD15"	Glycophosphatidylinositol anchor attachment protein 1	GPAA1	8733	ENSG00000197858		"Glycosylphosphatidylinositol biosynthesis defect 15, 617810 (3)"	Gpaa1 (MGI:1202392)			
chr8	144095034	144097526	8q24.3	8q24.3		123980	"CYC1, MC3DN6"	Cytochrome c1	CYC1	1537	ENSG00000179091		"Mitochondrial complex III deficiency, nuclear type 6, 615453 (3), Autosomal recessive"	Cyc1 (MGI:1913695)			
chr8	144098632	144104247	8q24.3	8q24.3		611885	"SHARPIN, SIPL1"	SHANK-associated RH domain interactor	SHARPIN	81858	ENSG00000179526			Sharpin (MGI:1913331)			
chr8	144104401	144107611	8q24.3	8q24.3		610210	MAF1	"Maf1, S. cerevisiae, homolog of"	MAF1	84232	ENSG00000179632			Maf1 (MGI:1916127)			
chr8	144262045	144291437	8q24	8q24.3		610596	"BOP1, KIAA0124"	Block of proliferation 1	BOP1	23246	ENSG00000261236			Bop1 (MGI:1334460)			
chr8	144265059	144268482	8q24.3	8q24.3		609067	"SCXA, SCX"	"Scleraxis, mouse, homolog of, A"	SCX	642658	ENSG00000260428			Scx (MGI:102934)			
chr8	144291568	144314725	8q24.3	8q24.3		140580	HSF1	Heat-shock transcription factor 1	HSF1	3297	ENSG00000185122			Hsf1 (MGI:96238)			
chr8	144314582	144326918	8q24.3	8q24.3		604900	"DGAT1, ARGP1, DIAR7"	Diacylglycerol O-acyltransferase 1	DGAT1	8694	ENSG00000185000	mutation identified in 1 DIAR7 family	"?Diarrhea 7, 615863 (3), Autosomal recessive"	Dgat1 (MGI:1333825)			
chr8	144330564	144336280	Chr.8	8q24.3		605858	SCRT1	"Scratch, mouse, homolog of"	SCRT1	83482	ENSG00000261678			Scrt1 (MGI:2176606)			
chr8	144355427	144358522	8q24.3	8q24.3		609076	"FBXL6, FBL6, FBL6A"	F-box and leucine-rich repeat protein 6	FBXL6	26233	ENSG00000182325			Fbxl6 (MGI:1354705)			
chr8	144358546	144361285	8q24.3	8q24.3		607882	"SLC52A2, GPR172A, GPCR41, PAR1, FLJ11856, BVVLS2"	"Solute carrier family 52, riboflavin transporter, member 2"	SLC52A2	79581	ENSG00000185803		"Brown-Vialetto-Van Laere syndrome 2, 614707 (3), Autosomal recessive"	Slc52a2 (MGI:1289288)			
chr8	144412413	144417145	8q24.3	8q24.3		607059	"SLC39A4, ZIP4"	"Solute carrier family 36 (zinc transporter), member 4"	SLC39A4	55630	ENSG00000147804		"Acrodermatitis enteropathica, 201100 (3), Autosomal recessive"	Slc39a4 (MGI:1919277)			
chr8	144423600	144428562	8q24.3	8q24.3		611952	VPS28	"Vacuolar protein sorting 28, yeast, homolog of"	VPS28	51160	ENSG00000160948			Vps28 (MGI:1914164)			
chr8	144428779	144444487	8q24.3	8q24.3		604546	"NFKBIL2, IKBR"	Nuclear factor of kappa light chain gene enhancer in B cells inhibitor-like 2	TONSL	4796	ENSG00000160949			Tonsl (MGI:1919999)			
chr8	144449581	144465647	8q24.3	8q24.3		616635	"CYHR1, KIAA0496"	Cysteine- and histidine-rich protein 1	CYHR1	50626	ENSG00000187954			Cyhr1 (MGI:1859320)			
chr8	144466245	144474115	8q24.3	8q24.3		615216	KIFC2	Kinesin family member C2	KIFC2	90990	ENSG00000167702			Kifc2 (MGI:109187)			
chr8	144473731	144476334	8q24.3	8q24.3		603621	FAST1	"Forkhead activin signal transducer 1, Xenopus, homolog of"	FOXH1	8928	ENSG00000160973			Foxh1 (MGI:1347465)			
chr8	144502216	144507173	8q24.3	8q24.3		138200	"GPT, GPT1, AAT1"	Glutamic-pyruvate transaminase (alanine aminotransferase)	GPT	2875	ENSG00000167701			Gpt (MGI:95802)			
chr8	144511283	144517827	8q24.3	8q24.3		603780	"RECQL4, RTS, RECQ4"	"DNA helicase, RecQ-like 4"	RECQL4	9401	ENSG00000160957		"Baller-Gerold syndrome, 218600 (3), Autosomal recessive; RAPADILINO syndrome, 266280 (3), Autosomal recessive; Rothmund-Thomson syndrome, 268400 (3), Autosomal recessive"	Recql4 (MGI:1931028)			
chr8	144529178	144700519	8q24.3	8q24.3		615880	"ARHGAP39, VILSE, KIAA1688"	RHO GTPase-activating protein 39	ARHGAP39	80728	ENSG00000147799			Arhgap39 (MGI:107858)			
chr8	144772223	144787370	8q24.12-q24.13	8q24.3		194526	"ZNF34, KOX32"	Zinc finger protein-34 (KOX32)	ZNF34	80778	ENSG00000196378						
chr8	144789764	144792445	8q	8q24.3		604177	RPL8	Ribosomal protein L8	RPL8	6132	ENSG00000161016			Rpl8 (MGI:1350927)			
chr8	144827508	144848069	8q24	8q24.3		194531	"ZNF7, KOX4"	Zinc finger protein-7 (KOX4)	ZNF7	7553	ENSG00000147789			Zfp7 (MGI:99208)			
chr8	144837977	144853577	8q24.3	8q24.3		608216	"COMMD5, HCARG"	COMM domain-containing protein 5	COMMD5	28991	ENSG00000170619			Commd5 (MGI:1913648)			
chr8	144930357	144950887	8q24	8q24.3		601262	"ZNF16, KOX9"	Zinc finger protein-16 (KOX 9)	ZNF16	7564	ENSG00000170631						
chr8	0	145138636	Chr.8			608392	"AIS3, VAMAS4"	"Autoimmune disease, susceptibility to, 3"	AIS3	378427			"{Autoimmune disease, susceptibility to, 3}, 608392 (2)"				
chr8	0	145138636	Chr.8			147860	IFNB3	"Interferon, beta-3, fibroblast"				previously assigned to 2p23-qter					
chr8	0	145138636	Chr.8			194490	ZNF1	Zinc finger protein-1									
chr9	0	43000000	9p			158170	"DEL9p, C9DELp"	Chromosome 9p deletion syndrome					"Chromosome 9p deletion syndrome, 158170 (4), Autosomal dominant"				
chr9	0	2200000	9p24.3			154230	"DEL9p24.3, C9DELp24.3, SRXY4"	Chromosome 9p24.3 deletion syndrome					"46XY sex reversal 4, 154230 (4)"				
chr9	0	43000000	9p			606613	HDLCQ1	High density lipoprotein cholesterol level QTL 1	HDLCQ1	192144			"[High density lipoprotein cholesterol level QTL 1], 606613 (2)"				
chr9	0	9000000	9p24			614113	MRD2	"Mental retardation, autosomal dominant 2"				2 patients reported with genomic deletion or rearrangement including disruption of DOCK8	"Mental retardation, autosomal dominant 2, 614113 (4), Autosomal dominant"				
chr9	0	19900000	9p24-p22			610438	RLS3	"Restless legs syndrome, susceptibility to, 3"		100188812		associated with rs4626664 and rs1975197	"{Restless legs syndrome 3}, 610438 (2)"				
chr9	14474	30486	9p24.3	9p24.3		613632	"WASHC1, WASH1"	"WASH complex, subunit 1"	WASHC1	100287171	ENSG00000181404	"pseudogenes on 1p, 15q, 16p, Xq/Yq"		Washc1 (MGI:1916017)			
chr9	116230	118416	9q21.11	9p24.3		601092	"FOXD4, FKHL9"	Forkhead box D4	FOXD4	2298	ENSG00000170122			Foxd4 (MGI:1347467)			
chr9	121037	179082	9p24.3	9p24.3		611078	CBWD1	Cobalamin synthetase W domain-containing protein 1	CBWD1	55871	ENSG00000172785			Cbwd1 (MGI:2385089)			
chr9	211295	465259	9p24	9p24.3		611432	DOCK8	Dedicator of cytokinesis 8	DOCK8	81704	ENSG00000107099		"Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3), Autosomal recessive"	Dock8 (MGI:1921396)			
chr9	470290	746105	9p24.3	9p24.3		607704	"KANK1, KANK, ANKRD15, KIAA0172, CPSQ2"	KN motif- and ankyrin repeat domain-containing protein 1	KANK1	23189	ENSG00000107104		"Cerebral palsy, spastic quadriplegic, 2, 612900 (3)"	Kank1 (MGI:2147707)			
chr9	841646	969089	9p24.3	9p24.3		602424	"DMRT1, DMT1"	Double sex and mab-3-related transcription factor-1	DMRT1	1761	ENSG00000137090			Dmrt1 (MGI:1354733)			
chr9	976967	991731	9p24.3	9p24.3		614754	"DMRT3, DMRTA3"	Doublesex-and mab3-related transcription factor 3	DMRT3	58524	ENSG00000064218			Dmrt3 (MGI:2449470)			
chr9	1003236	1057553	9p24.3	9p24.3		604935	DMRT2	Double sex and mab-3-related transcription factor-2	DMRT2	10655	ENSG00000173253			Dmrt2 (MGI:1330307)			
chr9	2015218	2193623	9p24-p23	9p24.3		600014	"SMARCA2, SNF2L2, NCBRS"	"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2"	SMARCA2	6595	ENSG00000080503		"Nicolaides-Baraitser syndrome, 601358 (3), Autosomal dominant"	Smarca2 (MGI:99603)			
chr9	2621773	2656102	9p24	9p24.2		192977	"VLDLR, CAMRQ1"	Very low density lipoprotein receptor	VLDLR	7436	ENSG00000147852		"Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, 224050 (3), Autosomal recessive"	Vldlr (MGI:98935)			
chr9	2717525	2730036	9p24.2	9p24.2		607604	"KCNV2, KV11.1, RCD3B"	"Potassium channel, voltage-gated, subfamily V, member 2"	KCNV2	169522	ENSG00000168263		"Retinal cone dystrophy 3B, 610356 (3), Autosomal recessive"	Kcnv2 (MGI:2670981)			
chr9	2804151	2844129	9p24.2	9p24.2		609960	"KIAA0020, HLA-HA8"	Minor histocompatibility antigen HA-8	PUM3	9933	ENSG00000080608			Pum3 (MGI:106253)			
chr9	3218296	3526528	9p24.2	9p24.2		601337	RFX3	"Regulatory factor X, 3"	RFX3	5991	ENSG00000080298			Rfx3 (MGI:106582)			
chr9	3824126	4310693	9p24.3-p23	9p24.2		610192	"GLIS3, ZNF515, NDH"	GLIS family zinc finger protein 3	GLIS3	169792	ENSG00000107249		"Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3), Autosomal recessive"	Glis3 (MGI:2444289)			
chr9	4490426	4587468	9p24	9p24.2		133550	"SLC1A1, EAAC1, SCZD18, DCBXA"	"Solute carrier family 1, member 1 (high-affinity glutamate transporter; excitatory amino acid carrier 1)"	SLC1A1	6505	ENSG00000106688	mutation identified in 1 SCZD18 family	"Dicarboxylic aminoaciduria, 222730 (3), Autosomal recessive; {?Schizophrenia susceptibility 18}, 615232 (3)"	Slc1a1 (MGI:105083)			
chr9	4600000	19900000	9p24.1-p22.1			613271	"FECD7, FCD4"	"Corneal dystrophy, Fuchs endothelial, 7"		100380875		max lod at D9S256	"Corneal dystrophy, Fuchs endothelial, 7, 613271 (2)"				
chr9	4662293	4665273	9p24.1	9p24.1		611666	"PLPP6, PPAPDC2"	PPAP2 domain-containing protein 2	PLPP6	403313	ENSG00000205808		"Phospholipid phosphatase 6, 611666 (3)"	Plpp6 (MGI:1921661)			
chr9	4679552	4708398	9p24.1	9p24.1		610346	"CDC37L1, HARC, FLJ20639"	CDC37-like 1	CDC37L1	55664	ENSG00000106993			Cdc37l1 (MGI:1914322)			
chr9	4709555	4742042	9p24.1	9p24.1		609290	"AK3, AK3L1"	Adenylate kinase 3	AK3	50808	ENSG00000147853			Ak3 (MGI:1860835)			
chr9	4792833	4861076	9p24.1	9p24.1		611405	"RCL1, RPCL1, RNAC"	RNA terminal phosphate cyclase-like 1	RCL1	10171	ENSG00000120158			Rcl1 (MGI:1913275)			
chr9	4850296	4850374	9p24.1	9p24.1		612512	"MIR101-2, MIRN101-2"	Micro RNA 101-2	MIR101-2	406894		"another locus, MIRN101-1, on 1p31"					
chr9	4985085	5128182	9p24	9p24.1		147796	"JAK2, THCYT3"	Janus kinase 2 (a protein-tyrosine kinase)	JAK2	3717	ENSG00000096968		"{Budd-Chiari syndrome, somatic}, 600880 (3); Erythrocytosis, somatic, 133100 (3); Leukemia, acute myeloid, somatic, 601626 (3); Myelofibrosis, somatic, 254450 (3); Polycythemia vera, somatic, 263300 (3); Thrombocythemia 3, 614521 (3), Autosomal dominant, Somatic mutation"	Jak2 (MGI:96629)			
chr9	4992408	5185706	9p24	9p24.1		606414	INSL6	Insulin-like 6	INSL6	11172	ENSG00000120210			Insl6 (MGI:1351595)			
chr9	5231418	5233966	9p24	9p24.1		600910	INSL4	"Insulin-like 4, placenta"	INSL4	3641	ENSG00000120211						
chr9	5299863	5340914	9pter-q12	9p24.1		179730	RLN1	"Relaxin, H1"	RLN1	6013	ENSG00000107018			Rln1 (MGI:97931)			
chr9	5299863	5339437	9pter-q12	9p24.1		179740	RLN2	"Relaxin, H2"	RLN2	6019	ENSG00000107014						
chr9	5450502	5470566	9p24	9p24.1		605402	"CD274, PDCD1LG1, B7H1"	CD274 molecule	CD274	29126	ENSG00000120217			Cd274 (MGI:1926446)			
chr9	5510437	5571281	9p24.2	9p24.1		605723	"PDCD1L2, PDL2"	Programmed cell death 1 ligand 2	PDCD1LG2	80380	ENSG00000197646			Pdcd1lg2 (MGI:1930125)			
chr9	5629029	5778632	9p24.1	9p24.1		610354	"CIP150, KIAA1432"	"Connexin 43-interacting protein, 150kD"	RIC1	57589	ENSG00000107036			Ric1 (MGI:1924893)			
chr9	5764060	5867090	9p24	9p24.1		611156	"ERMP1, KIAA1815, FXNA"	Endoplasmic reticulum metallopeptidase 1	ERMP1	79956	ENSG00000099219			Ermp1 (MGI:106250)			
chr9	5890908	5909821	9p24.1	9p24.1		605513	"MLANA, MART1"	Melan A	MLANA	2315	ENSG00000120215			Mlana (MGI:108454)			
chr9	6214590	6257982	9p24.1	9p24.1		608678	"IL33, C9orf26, NFEHEV"	Interleukin 33	IL33	90865	ENSG00000137033			Il33 (MGI:1924375)			
chr9	6328348	6331899	9p24.1	9p24.1		617567	TPD52L3	Tumor protein D52-like 3	TPD52L3	89882	ENSG00000170777			Trpd52l3 (MGI:1913995)			
chr9	6413147	6507055	9p24.1-p23	9p24.1		615211	"UHRF2, NIRF"	"Ubiquitin-like protein containing PDH and RING finger domains 2, E3 ubiquitin protein ligase"	UHRF2	115426	ENSG00000147854			Uhrf2 (MGI:1923718)			
chr9	6532463	6645691	9p22	9p24.1		238300	"GLDC, HYGN1, GCSP, GCE, NKH"	"Glycine dehydrogenase (decarboxylating; glycine decarboxylase, glycine cleavage system protein P)"	GLDC	2731	ENSG00000178445		"Glycine encephalopathy, 605899 (3), Autosomal recessive"	Gldc (MGI:1341155)			
chr9	6720862	7175647	9p24.1	9p24.1		605469	"KDM4C, JMJD2C, GASC1, KIAA0780"	Lysine-specific demethylase 4C	KDM4C	23081	ENSG00000107077			Kdm4c (MGI:1924054)			
chr9	7796489	7799805	9p24.1	9p24.1		617261	"TMEM261, DMAC1, C9orf123"	Transmembrane protein 261	DMAC1	90871	ENSG00000137038			Dmac1 (MGI:1914178)			
chr9	8314245	10612840	9p24.3-p23	9p24-p23		601598	"PTPRD, PTPD, HPTP"	"Protein tyrosine phosphatase, receptor type, delta polypeptide"	PTPRD	5789	ENSG00000153707						
chr9	9000000	28000000	9p23-p21.2			613685	DFNB83	"Deafness, autosomal recessive 83"	DFNB83	100359400		between rs4742645 and rs1471364	"Deafness, autosomal recessive 83, 613685 (2), Autosomal recessive"				
chr9	9000000	43000000	9p23-p11			601992	FRDA2	Friedreich ataxia 2	FRDA2	2420			"Friedreich ataxia 2, 601992 (2), Autosomal recessive"				
chr9	9000000	36300000	9p23-p13.3			614208	MRT16	"Mental retardation, autosomal recessive 16"		100689014		between rs10738277 and rs12376565	"Mental retardation, autosomal recessive 16, 614208 (2), Autosomal recessive"				
chr9	12693374	12710265	9p23	9p23		115501	"TYRP1, CAS2, GP75, SHEP11"	Tyrosinase-related protein 1	TYRP1	7306	ENSG00000107165		"Albinism, oculocutaneous, type III, 203290 (3), Autosomal recessive; [Skin/hair/eye pigmentation, variation in, 11 (Melanesian blond hair)], 612271 (3)"	Tyrp1 (MGI:98881)			
chr9	12774993	12823059	9p23	9p23		616130	"LURAP1L, LRAP35B"	Leucine-rich adaptor protein 1-like	LURAP1L	286343	ENSG00000153714			Lurap1l (MGI:106510)			
chr9	13105295	13279712	9p24-p22	9p23		603785	"MPDZ, MUPP1, HYC2"	Multiple PDZ domain protein	MPDZ	8777	ENSG00000107186		"Hydrocephalus, nonsyndromic, autosomal recessive 2, 615219 (3), Autosomal recessive"	Mpdz (MGI:1343489)			
chr9	14081842	14398982	9p24.1	9p23-p22		600728	NFIB	Nuclear factor I/B	NFIB	4781	ENSG00000147862			Nfib (MGI:103188)			
chr9	14200000	33200000	9p22-p21			608652	"DFNA47, DFNB83"	"Deafness, autosomal dominant 47"	DFNA47	246289		between D9S268 and D9S942; possibly allelic to DFNB83	"Deafness, autosomal dominant 47, 608652 (2), Autosomal dominant"				
chr9	14200000	33200000	9p22-p21			247640	LALL	Lymphomatous acute lymphoblastic leukemia		8009			"Leukemia, acute lymphoblastic, 247640 (2), Autosomal recessive"				
chr9	14588796	14693545	9p22.3	9p22.3		614605	"ZDHHC21, DHHC21"	Zinc finger DHHC domain-containing protein 21	ZDHHC21	340481	ENSG00000175893			Zdhhc21 (MGI:1915518)			
chr9	14715081	14724307	9p22	9p22.3		603777	CER1	"Cerebrus 1, Xenopus, homolog of"	CER1	9350	ENSG00000147869			Cer1 (MGI:1201414)			
chr9	14734665	14911652	9p22.3	9p22.3		608944	"FREM1, C9orf154, BNAR, MOTA, TRIGNO2"	FRAS1-related extracellular matrix protein 1	FREM1	158326	ENSG00000164946		"Bifid nose with or without anorectal and renal anomalies, 608980 (3); Manitoba oculotrichoanal syndrome, 248450 (3), Autosomal recessive; Trigonocephaly 2, 614485 (3), Autosomal dominant"	Frem1 (MGI:2670972)			
chr9	15167203	15307359	9p22.3	9p22.3		613574	TTC39B	Tetratricopeptide repeat domain 39B	TTC39B	158219	ENSG00000155158			Ttc39b (MGI:1917113)			
chr9	15422783	15466750	9p22.3	9p22.3		602348	"SNAPC3, SNAP50"	"Small nuclear RNA-activating protein complex, polypeptide 3"	SNAPC3	6619	ENSG00000164975			Snapc3 (MGI:1916338)			
chr9	15464065	15511018	9p22.2	9p22.3		603620	"PSIP1, LEDGF"	PC4- and SFRS1-interacting protein 1	PSIP1	11168	ENSG00000164985			Psip1 (MGI:2142116)			
chr9	16409502	16870787	9p22.1	9p22.3-p22.2		608669	BNC2	Basonuclin 2	BNC2	54796	ENSG00000173068			Bnc2 (MGI:2443805)			
chr9	17134990	17510019	9p22.2	9p22.2		611870	"CNTLN, C9orf101, C9orf39"	Centlein	CNTLN	54875	ENSG00000044459			Cntln (MGI:2443104)			
chr9	17578953	17797128	9p22	9p22.2		604465	"SH3GL2, SH3P4"	"SH3 domain, GRB2-like, 2"	SH3GL2	6456	ENSG00000107295			Sh3gl2 (MGI:700009)			
chr9	17906514	18910949	9p22.1-p21.2	9p22.2-p22.1		609198	ADAMTSL1	ADAMTS-like protein 1	ADAMTSL1	92949	ENSG00000178031			Adamtsl1 (MGI:1924989)			
chr9	18500000	19900000	9p22.1			609790	AD11	Alzheimer disease 11		100188795		between D9S157 and D9S259	"Alzheimer disease-11, 609790 (2)"				
chr9	18927659	19049505	9p22.1	9p22.1		616292	"SAXO1, FAM154A"	Stabilizer of axonemal microtubules 1	SAXO1	158297	ENSG00000155875			Saxo1 (MGI:1923061)			
chr9	19049373	19051024	9p22.1	9p22.1		612194	"RRAGA, RAGA, FIP1"	Ras-related GTP-binding protein A	RRAGA	10670	ENSG00000155876			Rraga (MGI:1915691)			
chr9	19053136	19102941	9p22.1	9p22.1		613433	"HAUS6, DGT6, FAM29A"	"HAUS, augmin-like complex, subunit 6"	HAUS6	54801	ENSG00000147874			Haus6 (MGI:1923389)			
chr9	19063655	19063785	9p22.1	9p22.1		615646	SCARNA8	Small Cajal body-specific RNA 8	SCARNA8	677776							
chr9	19108390	19127605	9p22.1	9p22.1		103195	PLIN2	Perilipin 2	PLIN2	123	ENSG00000147872			Plin2 (MGI:87920)			
chr9	19376255	19380236	9p21	9p22.1		180460	RPS6	Ribosomal protein S6	RPS6	6194	ENSG00000137154			Rps6 (MGI:98159)			
chr9	19408926	19455172	9p22.1	9p22.1		613492	ACER2	Alkaline ceramidase 2	ACER2	340485	ENSG00000177076			Acer2 (MGI:1920932)			
chr9	19507451	20307887	9p22	9p22.1-p21.3		609838	"SLC24A2, NCKX2"	"Solute carrier family 24 (sodium/potassium/calcium exchanger), member 2"	SLC24A2	25769	ENSG00000155886			Slc24a2 (MGI:1923626)			
chr9	19900000	33200000	9p21			611891	AAA3	"Aneurysm, familial abdominal 3"		100188857		associated with rs10757278	"{Aneurysm, familial abdominal 3}, 611891 (2)"				
chr9	19900000	33200000	9p21			611892	ANIB6	"Aneurysm, intracranial berry, 6"		100188858		associated with rs10757278	"{Aneurysm, intracranial berry, 6}, 611892 (2)"				
chr9	19900000	33200000	9p21			613062	BCC5	"Basal cell carcinoma, susceptibility to, 5"		100307122		associated with rs2151280	"{Basal cell carcinoma, susceptibility to, 5}, 613062 (2)"				
chr9	19900000	33200000	9p21			611139	CHDS8	"Coronary heart disease, susceptibility to, 8"		100188836		strongest linkage with dbSNP rs1333049	"{Coronary heart disease, susceptibility to, 8}, 611139 (2)"				
chr9	19900000	25600000	9p21.3			613030	GLM5	Glioma susceptibility 5		100415894		associated with rs4977756	"{Glioma susceptibility 5}, 613030 (2)"				
chr9	19900000	33200000	9p21			612099	"MFT2, TEM"	"Trichoepithelioma, multiple familial, 2"		100188881		max lod at D9S171	"Trichoepithelioma, multiple familial, 2, 612099 (2)"				
chr9	20341664	20622542	9p22	9p21.3		159558	"MLLT3, AF9"	"Myeloid/lymphoid or mixed-lineage leukemia, translocated to, 3"	MLLT3	4300	ENSG00000171843	fuses with ALL1		Mllt3 (MGI:1917372)			
chr9	20658308	20995954	9p21.3	9p21.3		614606	"FOCAD, KIAA1797"	Focadhesin	FOCAD	54914	ENSG00000188352			Focad (MGI:2676921)			
chr9	21003620	21031711	9p21.3	9p21.3		615941	"PTPLAD2, HACD4"	Protein tyrosine phosphatase-like A domain-containing protein 2	HACD4	401494	ENSG00000188921			Hacd4 (MGI:1914025)			
chr9	21077104	21077962	9p21	9p21.3		147640	IFNB1	"Interferon, beta-1, fibroblast"	IFNB1	3456	ENSG00000171855	distal to IFL; ?9p23-p22; IFF duplicate in some		Ifnb1 (MGI:107657)			
chr9	21140631	21141900	9p21	9p21.3		147553	IFNW1	"Interferon, omega-1"	IFNW1	3467	ENSG00000177047	pseudogene IFNWP2; interspersed with IFNA					
chr9	21165636	21166659	9p22	9p21.3		147584	IFNA21	"Interferon, alpha-21"	IFNA21	3452	ENSG00000137080						
chr9	21186617	21187598	9p22	9p21.3		147564	IFNA4	"Interferon, alpha-4"	IFNA4	3441	ENSG00000236637			"Ifnab,Ifna13,Ifna14,Ifna5,Ifna11,Ifna6,Ifna12,Ifna7,Ifna1,Ifna15,Ifna2,Ifna16,Ifna9 (MGI:107659,MGI:3649418,MGI:107666,MGI:107668,MGI:107661,MGI:107662,MGI:2676324,MGI:107663,MGI:3641425,MGI:109210,MGI:1097683,MGI:3649260,MGI:2667155)"			
chr9	21201468	21202204	9p22	9p21.3		147567	IFNA7	"Interferon, alpha-7"	IFNA7	3444	ENSG00000214042						
chr9	21206180	21207142	9p22	9p21.3		147577	IFNA10	"Interferon, alpha-10"	IFNA10	3446	ENSG00000186803						
chr9	21216372	21217310	9p22	9p21.3		147580	IFNA16	"Interferon, alpha-16"	IFNA16	3449	ENSG00000147885						
chr9	21227242	21228221	9p22	9p21.3		147583	IFNA17	"Interferon, alpha-17"	IFNA17	3451	ENSG00000234829						
chr9	21239201	21239978	9p22	9p21.3		147579	IFNA14	"Interferon, alpha-14"	IFNA14	3448	ENSG00000228083						
chr9	21304613	21305312	9p22	9p21.3		147565	IFNA5	"Interferon, alpha-5"	IFNA5	3442	ENSG00000147873						
chr9	21329670	21335431	9p21.3	9p21.3		611201	"KLHL9, KIAA1354"	Kelch-like 9	KLHL9	55958	ENSG00000198642			Klhl9 (MGI:2180122)			
chr9	21350317	21350886	9p22	9p21.3		147566	IFNA6	"Interferon, alpha-6"	IFNA6	3443	ENSG00000120235						
chr9	21367371	21368075	9p22	9p21.3		147578	IFNA13	"Interferon, alpha-13"	IFNA13	3447	ENSG00000233816						
chr9	21384254	21385396	9p22	9p21.3		147562	IFNA2	"Interferon, alpha-2"	IFNA2	3440	ENSG00000188379						
chr9	21409146	21410184	9p22	9p21.3		147568	IFNA8	"Interferon, alpha-8"	IFNA8	3445	ENSG00000120242						
chr9	21440453	21441315	9p22	9p21.3		147660	"IFNA1, IFNA@"	"Interferon, alpha-1"	IFNA1	3439	ENSG00000197919	"very close to IFF by Fd, LD; 15-30 genes"	"Interferon, alpha, deficiency (1)"				
chr9	21454267	21559797	9p21.3	9p21.3		616356	"MIR31HG, LOC554202"	"Micro RNA 31 host gene, noncoding"	MIR31HG	554202							
chr9	21480838	21482312	9p21	9p21.3		615223	"IFNE, INFE1, IFNT1"	"Interferon, epsilon"	IFNE	338376	ENSG00000184995			Ifne (MGI:2667156)			
chr9	21512114	21512184	9p21.3	9p21.3		612155	"MIR31, MIRN31"	Micro RNA 31	MIR31	407035							
chr9	21802635	21865970	9p21	9p21.3		156540	"MTAP, DMSMFH"	Methylthioadenosine phosphorylase	MTAP	4507	ENSG00000099810		"Diaphyseal medullary stenosis with malignant fibrous histiocytoma, 112250 (3), Autosomal dominant"	Mtap (MGI:1914152)			
chr9	21967751	21995042	9p21	9p21.3		600160	"CDKN2A, MTS1, P16, MLM, CMM2"	"Cyclin-dependent kinase inhibitor 2A (p16, inhibits CDK4)"	CDKN2A	1029	ENSG00000147889		"Melanoma and neural system tumor syndrome, 155755 (3), Autosomal dominant; {Melanoma, cutaneous malignant, 2}, 155601 (3), Autosomal dominant; Orolaryngeal cancer, multiple (3); Pancreatic cancer/melanoma syndrome, 606719 (3), Autosomal dominant"	Cdkn2a (MGI:104738)			
chr9	21994790	22121096	9p21	9p21.3		613149	"CDKN2BAS, ANRIL"	CDKN2B antisense RNA	CDKN2B-AS1	100048912							
chr9	22002902	22009312	9p21	9p21.3		600431	"CDKN2B, MTS2, P15, INK4B"	"Cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)"	CDKN2B	1030	ENSG00000147883	tandem with MTS1		Cdkn2b (MGI:104737)			
chr9	22446840	22452472	9p21.3	9p21.3		614803	"DMRTA1, DMRT4"	Doublesex- and MAB3-related transcription factor A1	DMRTA1	63951	ENSG00000176399			Dmrta1 (MGI:2653627)			
chr9	23690098	23850707	9p21	9p21.3		601673	"ELAVL2, HELN1, HUB"	"Embryonic lethal, abnormal vision, Drosophila, homolog of, like-2 (Hu antigen B)"	ELAVL2	1993	ENSG00000107105			Elavl2 (MGI:1100887)			
chr9	25600000	28000000	9p21.2			617651	EMICER1	"EQTN, MOB3B, IFNK, and C9orf72 enhancer RNA I, noncoding"									
chr9	25676388	25678857	9p21	9p21.2		610529	"TUSC1, TSG9"	Tumor suppressor candidate 1	TUSC1	286319	ENSG00000198680			Tusc1 (MGI:2684283)			
chr9	26903369	26947472	9p21.2	9p21.2		603873	"PLAA, PLAP, NDMSBA"	Phospholipase A2-activating protein	PLAA	9373	ENSG00000137055		"Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies, 617527 (3), Autosomal recessive"	Plaa (MGI:104810)			
chr9	26946989	27066133	9p21.2	9p21.2		608040	"IFT74, CCDC2, CMG1, BBS20"	"Intraflagellar transport 74, Chlamydomonas, homolog of"	IFT74	80173	ENSG00000096872	mutation identified in 1 BBS20 patient	"?Bardet-Biedl syndrome 20, 617119 (3), Autosomal recessive"	Ift74 (MGI:1914944)			
chr9	27109140	27230177	9p21	9p21.2		600221	"TEK, TIE2, VMCM, GLC3E"	"TEK tyrosine kinase, endothelial"	TEK	7010	ENSG00000120156		"Glaucoma 3, primary congenital, E, 617272 (3), Autosomal dominant; Venous malformations, multiple cutaneous and mucosal, 600195 (3), Autosomal dominant"	Tek (MGI:98664)			
chr9	27284653	27297138	9p21.2	9p21.2		617653	"EQTN, AFAF, SPACA8, C9orf11"	Equatorin	EQTN	54586	ENSG00000120160			Eqtn (MGI:1915003)			
chr9	27325208	27529851	9p21.2	9p21.2		617652	"MOB3B, MOB1D, MOBKL2B, C9orf35"	MOB kinase activator 3B	MOB3B	79817	ENSG00000120162			Mob3b (MGI:2664539)			
chr9	27524313	27526497	9p21.2	9p21.2		615326	IFNK	"Interferon, kappa"	IFNK	56832	ENSG00000147896			Ifnk (MGI:2683287)			
chr9	27546545	27573865	9p21	9p21.2		614260	"C9orf72, FTDALS1, FTDALS, ALSFTD"	Chromosome 9 open reading frame 72	C9orf72	203228	ENSG00000147894		"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 (3), Autosomal dominant"	3110043O21Rik (MGI:1920455)			
chr9	27937616	29215242	9p21.2-p21.1	9p21.2-p21.1		609793	"LRRN6C, LINGO2, LERN3"	"Leucine-rich repeat protein, neuronal, 6C"	LINGO2	158038	ENSG00000174482			Lingo2 (MGI:2442298)			
chr9	28888878	28888954	9p21.1	9p21.1		616137	MIR873	Micro RNA 873	MIR873	100126316							
chr9	32384602	32450835	9p21.2	9p21.1		100880	"ACO1, IREB1"	"Aconitase, soluble (iron-responsive element-binding protein-1)"	ACO1	48	ENSG00000122729			Aco1 (MGI:87879)			
chr9	32455301	32526323	9p21.1	9p21.1		609631	"DDX58, RIGI, SGMRT2"	DEAD box polypeptide 58	DDX58	23586	ENSG00000107201		"Singleton-Merten syndrome 2, 616298 (3), Autosomal dominant"	Ddx58 (MGI:2442858)			
chr9	32540543	32552627	9p21	9p21.1		609507	"TOPORS, P53BP3, LUN, RP31"	Topoisomerase I-binding arginine/serine-rich protein	TOPORS	10210	ENSG00000197579		"Retinitis pigmentosa 31, 609923 (3)"	Topors (MGI:2146189)			
chr9	32883871	33025130	9p13.3	9p21.1		606350	"APTX, AOA, AOA1"	Aprataxin	APTX	54840	ENSG00000137074		"Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia, 208920 (3), Autosomal recessive"	Aptx (MGI:1913658)			
chr9	33041851	33076715	9p21.1	9p21.1		617811	SMU1	DNA replication regulator and spliceosomal factor SMU1	SMU1	55234	ENSG00000122692			Smu1 (MGI:1915546)			
chr9	33110640	33167357	9p13	9p21.1		137060	"B4GALT1, GGTB2, GT1, GTB, CDG2D"	Glycoprotein-4-beta-galactosyltransferase-2 (EC 2.4.1.22)	B4GALT1	2683	ENSG00000086062		"Congenital disorder of glycosylation, type IId, 607091 (3), Autosomal recessive"	B4galt1 (MGI:95705)			
chr9	33200000	39000000	9p13			609403	PEE3	Preeclampsia/eclampsia 3		780909			"Preeclampsia/eclampsia 3, 609403 (2)"				
chr9	33240163	33248566	9p13.3	9p13.3		613929	"SPINK4, PEC60"	"Serine protease inhibitor, Kazal-type, 4"	SPINK4	27290	ENSG00000122711			Spink4 (MGI:1341848)			
chr9	33252470	33264760	9p12	9p13.3		601497	BAG1	BCL2-associated athanogene	BAG1	573	ENSG00000107262			Bag1 (MGI:108047)			
chr9	33264878	33282068	9p13.3	9p13.3		610900	CHMP5	"CHMP family, member 5"	CHMP5	51510	ENSG00000086065			Chmp5 (MGI:1924209)			
chr9	33290416	33371162	9p13.3	9p13.3		603255	NFX1	"Nuclear transcription factor, X box-binding, protein 1"	NFX1	4799	ENSG00000086102			Nfx1 (MGI:1921414)			
chr9	33383134	33402681	9p13	9p13.3		602974	"AQP7, GLYCQTL"	Aquaporin-7	AQP7	364	ENSG00000165269		"[Glycerol quantitative trait locus], 614411 (3), Autosomal recessive"	Aqp7 (MGI:1314647)			
chr9	33441153	33447632	9p13	9p13.3		600170	AQP3	Aquaporin-3	AQP3	360	ENSG00000165272	incorrectly mapped to chr.7	"[Blood group GIL], 607457 (3)"	Aqp3 (MGI:1333777)			
chr9	33460810	33473942	9p13	9p13.3		611532	"NOL6, NRAP"	Nucleolar protein 6	NOL6	65083	ENSG00000165271			Nol6 (MGI:2140151)			
chr9	33673503	33677419	9p13.3	9p13.3		613531	PTENP1	Phosphatase and tensin homolog pseudogene 1 (functional)	PTENP1	11191							
chr9	33750465	33799230	9p13	9p13.3		613578	"PRSS3, TRY3, T9"	"Protease, serine, 3"	PRSS3	5646	ENSG00000010438			"Try5,Try4 (MGI:102756,MGI:102757)"			
chr9	33817163	33920402	9p22.1	9p13.3		612506	"UBE2R2, UBC3B"	Ubiquitin-conjugating enzyme E2R 2	UBE2R2	54926	ENSG00000107341			Ube2r2 (MGI:1914865)			
chr9	34179004	34252522	9p22-p21	9p13.3		609787	"UBAP1, UBAP"	Ubiquitin-associated protein 1	UBAP1	51271	ENSG00000165006			Ubap1 (MGI:2149543)			
chr9	34252032	34333519	9p13.3	9p13.3		613747	KIF24	Kinesin family member 24	KIF24	347240	ENSG00000186638			Kif24 (MGI:1918345)			
chr9	34329505	34343712	9p13	9p13.3		602852	"NUDT2, APAH1"	Nudix-type motif 1 (AP4A hydrolase-1)	NUDT2	318	ENSG00000164978			Nudt2 (MGI:1913651)			
chr9	34458751	34520988	9p13.3	9p13.3		604366	"DNAI1, CILD1, ICS, PCD"	"Dynein, axonemal, intermediate chain 1"	DNAI1	27019	ENSG00000122735		"Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3), Autosomal recessive"	Dnaic1 (MGI:1916172)			
chr9	34551431	34590385	9p13	9p13.3		118946	CNTFR	Ciliary neurotrophic factor receptor	CNTFR	1271	ENSG00000122756			Cntfr (MGI:99605)			
chr9	34613544	34620522	9p13	9p13.3		607387	"DCTN3, DCTN22"	Dynactin 3	DCTN3	11258	ENSG00000137100			Dctn3 (MGI:1859251)			
chr9	34634721	34637825	9p13	9p13.3		601978	"SIGMAR1, SRBP, ALS16, DSMA2"	Sigma nonopioid intracellular receptor 1	SIGMAR1	10280	ENSG00000147955	mutation identified in 1 ALS16 family and 1 DSMA2 family	"?Amyotrophic lateral sclerosis 16, juvenile, 614373 (3), Autosomal recessive; ?Spinal muscular atrophy, distal, autosomal recessive, 2, 605726 (3), Autosomal recessive"	Sigmar1 (MGI:1195268)			
chr9	34646588	34650597	9p13	9p13.3		606999	GALT	Galactose-1-phosphate uridyltransferase	GALT	2592	ENSG00000213930		"Galactosemia, 230400 (3), Autosomal recessive"	Galt (MGI:95638)			
chr9	34652184	34661901	9p13	9p13.3		600939	"IL11RA, CRSDA"	"Interleukin-11 receptor, alpha"	IL11RA	3590	ENSG00000137070		"Craniosynostosis and dental anomalies, 614188 (3), Autosomal recessive"	"Il11ra1,Gm13305,Gm2002,Il11ra2 (MGI:3780172,MGI:107426,MGI:3801997,MGI:109123)"			
chr9	34661882	34662691	9p13	9p13.3		604833	"CCL27, SCYA27, ILC, CTACK"	"Chemokine, C-C motif, ligand 27"	CCL27	10850	ENSG00000213927			"Gm2506,Gm13306,Ccl27b (MGI:1891389,MGI:3713752,MGI:3780673)"			
chr9	34689569	34691276	9p13	9p13.3		602227	"CCL19, SCYA19, ELC, MIP3B"	"Chemokine, C-C motif, ligand 19"	CCL19	6363	ENSG00000172724			"Ccl19-ps1,Gm12407,Gm13309,Gm21104,Gm2457,Gm2564,Ccl19,Gm2023 (MGI:5434459,MGI:3708691,MGI:1891387,MGI:3780624,MGI:1346316,MGI:3780192,MGI:3693096,MGI:3702000)"			
chr9	34709004	34710166	9p13	9p13.3		602737	"CCL21, SCYA21, SLC"	"Chemokine, C-C motif, ligand 21"	CCL21	6366	ENSG00000137077			"Ccl21c,Gm1987,Gm13304,Gm10591,Ccl21b,Ccl21a,Gm21541 (MGI:1349183,MGI:3711256,MGI:1349182,MGI:5434896,MGI:3710514,MGI:1891386,MGI:3780156)"			
chr9	34989640	34998432	9p13.3	9p13.3		611328	"DNAJB5, KIAA1045, HSC40"	"DNAJ/HSP40 homolog, subfamily B, member 5"	DNAJB5	25822	ENSG00000137094			Dnajb5 (MGI:1930018)			
chr9	35056063	35072741	9p13-p12	9p13.3		601023	"VCP, IBMPFD1, ALS14, CMT2Y"	Valosin-containing protein	VCP	7415	ENSG00000165280		"Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954 (3); Charcot-Marie-Tooth disease, type 2Y, 616687 (3), Autosomal dominant; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320 (3), Autosomal dominant"	Vcp (MGI:99919)			
chr9	35073837	35080015	9p13	9p13.3		602956	"XRCC9, FANCG"	"X-ray repair, complementing defective, in Chinese hamster, 9"	FANCG	2189	ENSG00000221829		"Fanconi anemia, complementation group G, 614082 (3)"	Fancg (MGI:1926471)			
chr9	35085495	35096600	9p13	9p13.3		614730	"PIGO, HPMRS2"	"Phosphatidylinositol glycan, class O"	PIGO	84720	ENSG00000165282		"Hyperphosphatasia with mental retardation syndrome 2, 614749 (3), Autosomal recessive"	Pigo (MGI:1861452)			
chr9	35099775	35103194	9p13.1	9p13.3		608292	STOML2	Stomatin-like protein 2	STOML2	30968	ENSG00000165283			Stoml2 (MGI:1913842)			
chr9	35161968	35405337	Chr.9	9p13.3		605836	"UNC13, MUNC13"	"UNC13, C. elegans, homolog of"	UNC13B	10497	ENSG00000198722			Unc13b (MGI:1342278)			
chr9	35489832	35561897	9p13.1	9p13.3		611053	"RUSC2, KIAA0375, IPORIN, MRT61"	RUN and SH3 domain-containing 2	RUSC2	9853	ENSG00000198853		"Mental retardation, autosomal recessive 61, 617773 (3), Autosomal recessive"	Rusc2 (MGI:2140371)			
chr9	35605283	35610040	9p13	9p13.3		601782	TESK1	Testis-specific protein kinase-1	TESK1	7016	ENSG00000107140			Tesk1 (MGI:1201675)			
chr9	35609978	35618426	9p	9p13.3		107272	"CD72, LYB2"	CD72 antigen	CD72	971	ENSG00000137101			Cd72 (MGI:88345)			
chr9	35649297	35650949	9p13-p12	9p13.3		604964	SIT	SHP2-interacting transmembrane adaptor protein	SIT1	27240	ENSG00000137078			Sit1 (MGI:1889342)			
chr9	35657750	35658017	9p21-p12	9p13.3		157660	"RMRP, RMRPR, CHH"	Mitochondrial RNA-processing endoribonuclease	RMRP	6023			"Anauxetic dysplasia 1, 607095 (3), Autosomal recessive; Cartilage-hair hypoplasia, 250250 (3), Autosomal recessive; Metaphyseal dysplasia without hypotrichosis, 250460 (3), Autosomal recessive"				
chr9	35673808	35681158	9p13.3	9p13.3		603179	"CA9, MN"	Carbonic anhydrase IX	CA9	768	ENSG00000107159	previously assigned to 17q21.2		Car9 (MGI:2447188)			
chr9	35681992	35690055	9p13.2-p13.1	9p13.3		190990	"TPM2, TMSB, AMCD1, DA1, DA2B, NEM4"	"Tropomyosin-2, beta"	TPM2	7169	ENSG00000198467		"Arthrogryposis multiplex congenita, distal, type 1, 108120 (3), Autosomal dominant; Arthrogryposis, distal, type 2B, 601680 (3), Autosomal dominant; CAP myopathy 2, 609285 (3), Autosomal dominant; Nemaline myopathy 4, autosomal dominant, 609285 (3), Autosomal dominant"				
chr9	35697336	35732394	9p	9p13.3		186745	TLN1	Talin 1	TLN1	7094	ENSG00000137076			Tln1 (MGI:1099832)			
chr9	35732319	35737007	9p13.3	9p13.3		606443	"CREB3, LZIP"	cAMP response element-binding protein 3	CREB3	10488	ENSG00000107175			Creb3 (MGI:99946)			
chr9	35736861	35749235	9p13.3	9p13.3		609471	"GBA2, KIAA1605, SPG46"	"Glucosidase, beta, acid 2"	GBA2	57704	ENSG00000070610		"Spastic paraplegia 46, autosomal recessive, 614409 (3), Autosomal recessive"	Gba2 (MGI:2654325)			
chr9	35749279	35753266	9p13.3	9p13.3		615742	"RGP1, KIAA0258"	"RGP1 retrograde golgi transport, S. cerevisiae, homolog of"	RGP1	9827	ENSG00000107185			Rgp1 (MGI:1915956)			
chr9	35752989	35754276	9p13.3	9p13.3		612191	"MSMP, PSMP"	"Microseminoprotein, prostate-associated"	MSMP	692094	ENSG00000215183			Msmp (MGI:3652339)			
chr9	35782085	35809730	9p21-p12	9p13.3		108961	"NPR2, ANPRB, AMDM, ECDM, SNSK"	Natiuretic peptide receptor 2	NPR2	4882	ENSG00000159899		"Acromesomelic dysplasia, Maroteaux type, 602875 (3), Autosomal recessive; Epiphyseal chondrodysplasia, Miura type, 615923 (3), Autosomal dominant; Short stature with nonspecific skeletal abnormalities, 616255 (3), Autosomal dominant"	Npr2 (MGI:97372)			
chr9	35807784	35812271	9p13-p12	9p13.3		605731	"SPAG8, SMP1"	Sperm-associated antigen 8	SPAG8	26206	ENSG00000137098			Spag8 (MGI:3056295)			
chr9	35812959	35815478	9p11.2	9p13.3		609997	HINT2	Histidine triad nucleotide-binding protein 2	HINT2	84681	ENSG00000137133			Hint2 (MGI:1916167)			
chr9	35825816	35865514	9p13.3	9p13.3		616888	"TMEM8B, NGX6, NAG5"	Transmembrane protein 8B	TMEM8B	51754	ENSG00000137103			Tmem8b (MGI:2441680)			
chr9	35909482	35911619	9p13.3	9p13.3		617627	"SPAAR, LINC00961"	Small regulatory polypeptide of amino acid response	SPAAR	158376	ENSG00000235387						
chr9	36036904	36124454	9p13-p12	9p13.3		605227	"RECK, ST15"	Reversion-inducing cysteine-rich protein with kazal motifs (suppressor of tumorigenicity 15)	RECK	8434	ENSG00000122707			Reck (MGI:1855698)			
chr9	36136535	36163912	9p13.3	9p13.3		607141	"GLIPR2, GAPR1, C9orf19"	GLI pathogenesis-related 2	GLIPR2	152007	ENSG00000122694			Glipr2 (MGI:1917770)			
chr9	36169391	36171333	9p13.3	9p13.3		603960	CCIN	Calicin	CCIN	881	ENSG00000185972			Ccin (MGI:3045316)			
chr9	36190854	36212061	9p13.3	9p13.3		118960	CLTA	"Clathrin, light polypeptide (Lca)"	CLTA	1211	ENSG00000122705	previously mapped to 12q23-q24		Clta (MGI:894297)			
chr9	36214440	36277055	9p13.3	9p13.3		603824	"GNE, GLCNE, IBM2, DMRV, NM"	UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	GNE	10020	ENSG00000159921		"Nonaka myopathy, 605820 (3), Autosomal recessive; Sialuria, 269921 (3), Autosomal dominant"	Gne (MGI:1354951)			
chr9	36336397	36487383	9p13	9p13.2		612488	RNF38	Ring finger protein 38	RNF38	152006	ENSG00000137075			Rnf38 (MGI:1920719)			
chr9	36572861	36677682	Chr.9	9p13.2		607025	"MELK, KIAA0175"	Maternal embryonic leucine zipper kinase	MELK	9833	ENSG00000165304			Melk (MGI:106924)			
chr9	36833274	37034478	9p13	9p13.2		167414	"PAX5, BSAP, ALL3"	Paired box homeotic gene-5 (B-cell lineage specific activator protein)	PAX5	5079	ENSG00000196092		"{Leukemia, acute lymphoblastic, susceptibility to, 3}, 615545 (3)"	Pax5 (MGI:97489)			
chr9	37422434	37438951	9cen	9p13.2		604296	"GRHPR, GLXR"	Glyoxylate reductase/hydroxypyruvate reductase	GRHPR	9380	ENSG00000137106		"Hyperoxaluria, primary, type II, 260000 (3), Autosomal recessive"	Grhpr (MGI:1923488)			
chr9	37438101	37465409	9p13.2	9p13.2		616590	"ZBTB5, KIAA0354"	Zinc finger- and BTB domain-containing protein 5	ZBTB5	9925	ENSG00000168795			Zbtb5 (MGI:1924601)			
chr9	37510891	37576458	9p13.1	9p13.2		609092	"FBXO10, FBX10"	F-box only protein 10	FBXO10	26267	ENSG00000147912			Fbxo10 (MGI:2686937)			
chr9	37588412	37592638	9p13.2	9p13.2		616169	"TOMM5, TOM5"	"Translocase of outer mitochondrial membrane 5, yeast, homolog of"	TOMM5	401505	ENSG00000175768						
chr9	37602976	37746903	9p13.2	9p13.2		616919	"FRMPD1, FRMD2, KIAA0967"	FERM and PDZ domains-containing protein 1	FRMPD1	22844	ENSG00000070601			Frmpd1 (MGI:2446274)			
chr9	37779713	37785091	9p13.2	9p13.2		606489	"EXOSC3, RRP40, PCH1B"	Exosome component 3	EXOSC3	51010	ENSG00000107371		"Pontocerebellar hypoplasia, type 1B, 614678 (3), Autosomal recessive"	Exosc3 (MGI:1913612)			
chr9	37900000	69300000	9p13.1-q21.11			612096	OTSC8	Otosclerosis 8	OTSC8	100151644		between D9S970 and D9S1799	"Otosclerosis 8, 612096 (2), Autosomal dominant"				
chr9	37915897	38069212	9p12-p11	9p13.1		600314	SHB	SHB adaptor protein (a Src homology 2 protein)	SHB	6461	ENSG00000107338			Shb (MGI:98294)			
chr9	38392663	38398664	9p13	9p13.1		100670	"ALDH1B1, ALDH5"	"Aldehyde dehydrogenase 1 family, member B1"	ALDH1B1	219	ENSG00000137124			Aldh1b1 (MGI:1919785)			
chr9	38406527	38424446	9p13.1	9p13.1		610413	"IGFBPL1, IGFBPRP4"	Insulin-like growth factor binding protein-like 1	IGFBPL1	347252	ENSG00000137142			Igfbpl1 (MGI:1933198)			
chr9	39000000	61500000	9p12-q12			605388	ACP	"Cerebral palsy, ataxic, autosomal recessive"	CPAT1	60502			"Cerebral palsy, ataxic, autosomal recessive, 605388 (2), Autosomal recessive"				
chr9	39072766	39288302	9p13.1	9p12		610517	"CNTNAP3, KIAA1714"	Contactin-associated protein-like 3	CNTNAP3	79937	ENSG00000106714			Cntnap3 (MGI:3588199)			
chr9	40000000	43000000	9p11			155900	MROS	Melkersson-Rosenthal syndrome	MROS	8011			"?Melkersson-Rosenthal syndrome, 155900 (2), Autosomal dominant"				
chr9	43000000	138394717	9q			609320	HCHGQ2	Hematocrit/hemoglobin quantitative trait locus 2		100381205			"[Hematocrit/hemoglobin quantitative trait locus 2], 609320 (2)"				
chr9	43000000	138394717	9q			607152	SPG19	Spastic paraplegia-19	SPG19	140907			"Spastic paraplegia 19, autosomal dominant, 607152 (2), Autosomal dominant"				
chr9	45500000	61500000	9q12			126330	DNCM	Cytoplasmic membrane DNA		1784		in 9qh					
chr9	61190035	61196279	9q12	9q12		616584	"SPATA31A7, AEP1, FAM75A7, C9orf36"	"Spermatogenesis-associated protein 31, subfamily A, member 7"	SPATA31A7	26165	ENSG00000276040			Spata31 (MGI:1925374)			
chr9	61500000	65000000	9q13			600884	"CMD1B, CMPD1, FDC"	"Cardiomyopathy, dilated-1B, autosomal dominant"	CMD1B	1218			"Cardiomyopathy, dilated 1B, 600884 (2), Autosomal dominant"				
chr9	61500000	99800000	9q13-q22			605749	"CTRCT26, CAAR"	"Cataract 26, multiple types"	CTPL1	81863			"Cataract 26, multiple types, 605749 (2)"				
chr9	61500000	87800000	9q13-q21			190100	"GSM1, GSP"	Geniospasm 1	GSM1	2933			"Geniospasm, 190100 (2), Autosomal dominant"				
chr9	65000000	69300000	9q21.11			613558	"DFNA51, C9DUPq21.11, DUP9q21.11"	"Deafness, autosomal dominant 51 (chromosome 9q21.11 duplication syndrome)"				259kb duplication involving TJP2 and FAM189A2	"Deafness, autosomal dominant 51, 613558 (4), Autosomal dominant"				
chr9	65000000	99800000	9q21-q22			611631	"ETL4, ETOLM"	"Epilepsy, familial temporal lobe, 4"		100144434		between GATA152H04 and D9S253	"Epilepsy, familial temporal lobe, 4, 611631 (2), Autosomal dominant"				
chr9	65000000	87800000	9q21			613088	PVOP2	"Pelvic organ prolapse, susceptibility to, 2"		100312955		between rs4077632 and rs10868525	"{Pelvic organ prolapse, susceptibility to, 2}, 613088 (2)"				
chr9	65737145	65738395	9p11.2	9q21.11		611085	"FOXD4L4, FOXD4L2"	Forkhead box D4-like 4	FOXD4L4	349334	ENSG00000184659						
chr9	66900724	66932140	9q21.11	9q21.11		616290	ZNF658	Zinc finger protein 658	ZNF658	26149	ENSG00000274349			"Gm7145,Zfp735,Zfp616 (MGI:3648947,MGI:1923640,MGI:3650906)"			
chr9	68241865	68300034	9q13	9q21.11		611080	CBWD3	Cobalamin synthetase W domain-containing protein 3	CBWD3	445571	ENSG00000196873						
chr9	68302866	68305083	9q13	9q21.11		611086	FOXD4L3	Forkhead box D4-like 3	FOXD4L3	286380	ENSG00000187559						
chr9	68356583	68531060	9p12-q12	9q21.11		600981	PGM5	Phosphoglucomutase-5	PGM5	5239	ENSG00000154330			Pgm5 (MGI:1925668)			
chr9	68705216	69009175	9q13	9q21.11		602745	"PIP5K1B, STM7, MSS4"	"Phosphatidylinositol-4-phosphate 5-kinase, type I, beta"	PIP5K1B	8395	ENSG00000107242			Pip5k1b (MGI:107930)			
chr9	68780005	68783878	9q21.1	9q21.11		617249	"FAM122A, C9orf42"	"Family with sequence similarity 122, member A"	FAM122A	116224	ENSG00000187866			Fam122a (MGI:1915284)			
chr9	69012528	69014122	9q21.11	9q21.11		176893	"PRKACG, BDPLT19"	"Protein kinase, cAMP-dependent, catalytic, gamma"	PRKACG	5568	ENSG00000165059	mutation identified in 1 BDPLT19 family	"?Bleeding disorder, platelet-type, 19, 616176 (3), Autosomal recessive"				
chr9	69035562	69079076	9q13	9q21.11		606829	"FXN, FRDA, FARR, X25"	Frataxin	FXN	2395	ENSG00000165060		"Friedreich ataxia, 229300 (3), Autosomal recessive; Friedreich ataxia with retained reflexes, 229300 (3), Autosomal recessive"	Fxn (MGI:1096879)			
chr9	69121005	69255207	9q12-q13	9q21.11		607709	"TJP2, ZO2, PFIC4"	Tight junction protein 2	TJP2	9414	ENSG00000119139		"Cholestasis, progressive familial intrahepatic 4, 615878 (3), Autosomal recessive; Hypercholanemia, familial, 607748 (3)"	Tjp2 (MGI:1341872)			
chr9	69324571	69392472	9q13-q21	9q21.12		607710	X123	X123 gene	FAM189A2	9413	ENSG00000135063			Fam189a2 (MGI:2685813)			
chr9	69427531	69673011	9q21.11-q21.12	9q21.12		602414	"APBA1, X11, D9S411E, MINT1, LIN10"	"Amyloid beta A4 precursor protein-binding, family A, member 1"	APBA1	320	ENSG00000107282			Apba1 (MGI:1860297)			
chr9	70043580	70226971	9q21.11	9q21.12		612879	MAMDC2	MAM domain-containing 2	MAMDC2	256691	ENSG00000165072			Mamdc2 (MGI:1918988)			
chr9	70258961	70354872	9q21.11	9q21.12		609386	"SMC5L1, SMC5, KIAA0594"	Structural maintenance of chromosomes 5-like 1	SMC5	23137	ENSG00000198887			Smc5 (MGI:2385088)			
chr9	70384596	70414656	9q13	9q21.12		602902	"BTEB1, BTEB"	Basic transcription element-binding protein 1	KLF9	687	ENSG00000119138			Klf9 (MGI:1333856)			
chr9	70529062	71446949	9q21.12	9q21.12-q21.13		608961	"TRPM3, MLSN2, LTRPC3, KIAA1616"	"Transient receptor potential cation channel, subfamily M, member 3"	TRPM3	80036	ENSG00000083067			Trpm3 (MGI:2443101)			
chr9	70809974	70810083	9q21.11	9q21.12		610942	"MIR204, MIRN204, RDICC"	Micro RNA 204	MIR204	406987		mutation identified in 1 RDICC family	"?Retinal dystrophy and iris coloboma with or without cataract, 616722 (3), Autosomal dominant"				
chr9	71683365	71769531	9q13-q21	9q21.13		605835	TMEM2	Transmembrane protein 2	CEMIP2	23670	ENSG00000135048			Tmem2 (MGI:1890373)			
chr9	72114594	72256044	9q21.13	9q21.13		139260	"GDA, CYPIN"	Guanine deaminase	GDA	9615	ENSG00000119125			Gda (MGI:95678)			
chr9	72351424	72365246	9q13-q21	9q21.13		604761	"ZFAND5, ZNF216"	Zinc finger AN1 domain-containing protein 5	ZFAND5	7763	ENSG00000107372			Zfand5 (MGI:1278334)			
chr9	72521800	72836350	9q13-q21	9q21.13		606706	"TMC1, DFNB7, DFNB11, DFNA36"	Transmembrane channel-like protein 1	TMC1	117531	ENSG00000165091		"Deafness, autosomal dominant 36, 606705 (3), Autosomal dominant; Deafness, autosomal recessive 7, 600974 (3), Autosomal recessive"	Tmc1 (MGI:2151016)			
chr9	72900661	72953316	9q21	9q21.13		100640	ALDH1A1	"Aldehyde dehydrogenase-1 family, member A1, soluble"	ALDH1A1	216	ENSG00000165092			Aldh1a1 (MGI:1353450)			
chr9	73151730	73170392	9q11-q22	9q21.13		151690	"ANXA1, LPC1"	Annexin A1 (lipocortin I)	ANXA1	301	ENSG00000135046			Anxa1 (MGI:96819)			
chr9	74497335	74687200	9q22	9q21.13		601972	"RORB, RZRB"	RAR-related orphan receptor B	RORB	6096	ENSG00000198963			Rorb (MGI:1343464)			
chr9	74722494	74888093	9q22	9q21.13		607009	"TRPM6, CHAK2, HOMG1"	"Transient receptor potential cation channel, subfamily M, member 6"	TRPM6	140803	ENSG00000119121		"Hypomagnesemia 1, intestinal, 602014 (3), Autosomal recessive"	Trpm6 (MGI:2675603)			
chr9	74980793	75028455	9q21.13	9q21.13		616552	"CARNMT1, C9orf41, UPF0586"	Carnosine N-methyltransferase 1	CARNMT1	138199	ENSG00000156017			Carnmt1 (MGI:1914633)			
chr9	75088479	75147197	9q21.13	9q21.13		610180	"OSTF1, OSF, SH3P2"	Osteoclast-stimulating factor 1	OSTF1	26578	ENSG00000134996			Ostf1 (MGI:700012)			
chr9	75890643	76362338	9q21.3	9q21.13		600488	PCSK5	Proprotein convertase subtilisin/kexin type 5	PCSK5	5125	ENSG00000099139	?close to LPC1 on 9q		Pcsk5 (MGI:97515)			
chr9	76385516	76394527	9q21.1	9q21.13		613010	RFK	Riboflavin kinase	RFK	55312	ENSG00000135002			Rfk (MGI:1914688)			
chr9	76441665	76507415	9q13	9q21.13		600391	GCNT1	"Glucosaminyl (N-acetyl) transferase 1, core 2 (beta-1,6-N-acetylglucosaminyltransferase)"	GCNT1	2650	ENSG00000187210			Gcnt1 (MGI:95676)			
chr9	76611375	76906219	9p13	9q21.2		610691	"PRUNE2, BMCC1, KIAA0367"	"PRUNE, Drosophila, homolog of, 2"	PRUNE2	158471	ENSG00000106772			Prune2 (MGI:1925004)			
chr9	76764435	76787568	9q21-q22	9q21.2		604845	"PCA3, DD3"	Prostate cancer antigen 3	PCA3	50652							
chr9	77177352	77421536	9q21	9q21.2		605978	"VPS13A, CHAC"	Vacuolar protein sorting 13A (chorein)	VPS13A	23230	ENSG00000197969		"Choreoacanthocytosis, 200150 (3), Autosomal recessive"	Vps13a (MGI:2444304)			
chr9	77423078	77648315	9q21	9q21.2		604397	GNA14	"Guanine nucleotide-binding protein, alpha-14"	GNA14	9630	ENSG00000156049			Gna14 (MGI:95769)			
chr9	77716273	78031448	9q21	9q21.2		600998	"GNAQ, SWS, CMC1"	"Guanine nucleotide-binding protein (G protein), q"	GNAQ	2776	ENSG00000156052	pseudogene on 2q	"Capillary malformations, congenital, 1, somatic, mosaic, 163000 (3); Sturge-Weber syndrome, somatic, mosaic, 185300 (3)"	Gnaq (MGI:95776)			
chr9	78236061	78278436	9q21.2	9q21.2		617110	"CEP78, CRDHL"	"Centrosomal protein, 78kD"	CEP78	84131	ENSG00000148019		"Cone-rod dystrophy and hearing loss, 617236 (3), Autosomal recessive"	Cep78 (MGI:1924386)			
chr9	78297074	78330092	9q21.31	9q21.2		610936	"PSAT1, PSAT, EPIP, PSATD, NLS2"	Phosphoserine aminotransferase 1	PSAT1	29968	ENSG00000135069	mutation identified in 1 PSATD family	"Neu-Laxova syndrome 2, 616038 (3), Autosomal recessive; ?Phosphoserine aminotransferase deficiency, 610992 (3), Autosomal recessive"	Psat1 (MGI:2183441)			
chr9	78500000	99800000	9q21.3-q22			267700	"FHL1, HPLH1, HLH1"	"Hemophagocytic lymphohistiocytosis, familial, 1"	HPLH1	27259			"Hemophagocytic lymphohistiocytosis, familial, 1, 267700 (2), Autosomal recessive"				
chr9	81583682	81689534	9q21.3	9q21.32		600189	"TLE1, ESG1"	Transducin-like enhancer of split 1 (homolog of Drosophila E(spl))	TLE1	7088	ENSG00000196781	conflicting assignment to chr.19		Tle1 (MGI:104636)			
chr9	82979584	83063171	9q21.32	9q21.32		611344	RASEF	RAS and EF-hand domains-containing protein	RASEF	158158	ENSG00000165105			Rasef (MGI:2448565)			
chr9	83242989	83585796	9q21-q22	9q21.32		607619	"FRMD3, EPB41LO"	FERM domain-containing 3	FRMD3	257019	ENSG00000172159			Frmd3 (MGI:2442466)			
chr9	83622323	83644129	9q21.32	9q21.32		611343	C9orf103	Chromosome 9 open reading frame 103	IDNK	414328	ENSG00000148057			Idnk (MGI:1922981)			
chr9	83659962	83708252	9q21.2-q21.3	9q21.32		605046	"UBQLN1, DA41"	"Ubiquilin 1 (Da41, rat, homolog of)"	UBQLN1	29979	ENSG00000135018			Ubqln1 (MGI:1860276)			
chr9	83739420	83817836	9q21.32	9q21.32		611356	"GKAP1, GKAP42"	G kinase-anchoring protein 1	GKAP1	80318	ENSG00000165113			Gkap1 (MGI:1891694)			
chr9	83832794	83921543	9q21.32	9q21.32		611253	KIF27	Kinesin family member 27	KIF27	55582	ENSG00000165115			Kif27 (MGI:1922300)			
chr9	83938310	83956985	9q21.32	9q21.32		611342	C9orf64	Chromosome 9 open reading frame 64	C9orf64	84267	ENSG00000165118			2210016F16Rik (MGI:1917403)			
chr9	83968082	83980781	9q21.32-q21.33	9q21.32		600712	"HNRNPK, HNRPK, AUKS"	Heterogeneous nuclear ribonucleoprotein K	HNRNPK	3190	ENSG00000165119		"Au-Kline syndrome, 616580 (3), Autosomal dominant"	Hnrnpk (MGI:99894)			
chr9	83969747	83969856	9q21.32	9q21.32		615239	MIR7-1	Micro RNA 7-1	MIR7-1	407043							
chr9	83980358	84004073	9q21.32	9q21.32		610404	"RMI2, BLAP75, C9orf76"	"RecQ-mediated genome instability 1, S. cerevisiae, homolog of"	RMI1	80010	ENSG00000178966			Rmi1 (MGI:1921636)			
chr9	84273122	84368633	9q22.2	9q21.32-q21.33		608269	"SLC28A3, CNT3"	"Solute carrier family (sodium-coupled nucleoside transporter), member 3"	SLC28A3	64078	ENSG00000197506			Slc28a3 (MGI:2137361)			
chr9	84668457	85027069	9q21.33	9q21.33		600456	"NTRK2, TRKB, OBHD, EIEE58"	"Neurotrophic tyrosine kinase, receptor, type 2"	NTRK2	4915	ENSG00000148053		"Epileptic encephalopathy, early infantile, 58, 617830 (3), Autosomal dominant; Obesity, hyperphagia, and developmental delay, 613886 (3), Autosomal dominant"	Ntrk2 (MGI:97384)			
chr9	85546538	85742028	9q21.33	9q21.33		606830	"AGTPBP1, NNA1, KIAA1035, CCP1"	ATP/GTP-binding protein 1	AGTPBP1	23287	ENSG00000135049			Agtpbp1 (MGI:2159437)			
chr9	86026140	86100200	9q21.33	9q21.33		606804	"GOLM1, GOLPH2, GP73, C9orf155"	Golgi membrane protein 1	GOLM1	51280	ENSG00000135052			Golm1 (MGI:1917329)			
chr9	86264545	86282574	9q21.2-q22.1	9q21.33		611006	"ISCA1, HBLD2, HISCA, MMDS5"	"Iron-sulfur cluster assembly 1, S. cerevisiae, homolog of"	ISCA1	81689	ENSG00000135070		"Multiple mitochondrial dysfunctions syndrome 5, 617613 (3), Autosomal recessive"	Isca1 (MGI:1916296)			
chr9	86287732	86354496	9q21.33	9q21.33		613467	"ZCCHC6, TUT7, KIAA1711"	Zinc finger CCHC domain-containing protein 6	ZCCHC6	79670	ENSG00000083223			Zcchc6 (MGI:2387179)			
chr9	86944361	86947188	9q21.3-q22.1	9q21.33		139185	GAS1	Growth arrest-specific gene-1	GAS1	2619	ENSG00000180447			Gas1 (MGI:95655)			
chr9	87497227	87708633	9q34.1	9q21.33		600831	DAPK1	Death-associated protein kinase-1	DAPK1	1612	ENSG00000196730			Dapk1 (MGI:1916885)			
chr9	87725436	87731468	9q21-q22	9q21.33		116880	CTSL	Cathepsin L	CTSL	1514	ENSG00000135047	\'like\' sequence on 10q23-q24					
chr9	87800000	99800000	9q22			608695	JOAG2	"Glaucoma, primary open angle, juvenile-onset, 2"	GLC1J	574078		between D9S1803 and D9S196	"Glaucoma, primary open angle, juvenile-onset, 2, 608695 (2)"				
chr9	87800000	99800000	9q22			610114	STQTL8	Stature quantitative trait locus 8		100037266		between GATA81C04M and ATA18A07M	"{Stature QTL 8}, 610114 (2)"				
chr9	87966440	87974779	9q22.1	9q22.1		610076	"CDK20, CCRK, CDCH, P42"	Cyclin-dependent kinase 20	CDK20	23552	ENSG00000156345			Cdk20 (MGI:2145349)			
chr9	88388381	88478707	9q22.1-q22.3	9q22.1		609936	"SPIN, SPIN1"	Spindlin	SPIN1	10927	ENSG00000106723			Spin1 (MGI:109242)			
chr9	88535087	88584509	9q22.1	9q22.1		615299	"NXNL2, RDCVF2"	Nucleoredoxin-like protein 2	NXNL2	158046	ENSG00000130045			Nxnl2 (MGI:1922374)			
chr9	88991408	89005154	9q22.1-q22.2	9q22.1		601965	"S1PR3, EDG3"	Sphingosine-1-phosphate receptor 3	S1PR3	1903	ENSG00000213694			S1pr3 (MGI:1339365)			
chr9	89005770	89182401	9q22.1	9q22.1		605263	"SHC3, NSHC, RAI, SHCC"	SHC transforming protein 3	SHC3	53358	ENSG00000148082			Shc3 (MGI:106179)			
chr9	89311194	89316702	9q22.2	9q22.2		116901	CKS2	CDC2-associated protein CKS2	CKS2	1164	ENSG00000123975			Cks2 (MGI:1913447)			
chr9	89318472	89367116	9q22.2	9q22.2		607693	"SECISBP2, SBP2"	Selenocysteine insertion sequence-binding protein 2	SECISBP2	79048	ENSG00000187742		"Thyroid hormone metabolism, abnormal, 609698 (3)"	Secisbp2 (MGI:1922670)			
chr9	89360790	89498064	9q22.2	9q22.2		601866	"SEMA4D, SEMAJ, CD100, COLL4"	Semaphorin 4D	SEMA4D	10507	ENSG00000187764			Sema4d (MGI:109244)			
chr9	89605008	89606554	9q22.1-q22.2	9q22.2		604949	"GADD45G, GRP17"	"Growth arrest- and DNA damage-inducible gene 45, gamma"	GADD45G	10912	ENSG00000130222			Gadd45g (MGI:1346325)			
chr9	90609831	90643104	9q22.2	9q22.2		607863	DIRAS2	"DIRAS family, GTP-binding Ras-like protein 2"	DIRAS2	54769	ENSG00000165023			Diras2 (MGI:1915453)			
chr9	90801679	90898559	9q22	9q22.2		600085	SYK	Spleen tyrosine kinase	SYK	6850	ENSG00000165025			Syk (MGI:99515)			
chr9	91213814	91361968	9q22.31	9q22.31		600529	AUH	AU-specific RNA-binding protein (3-methylglutaconyl-CoA hydratase)	AUH	549	ENSG00000148090		"3-methylglutaconic aciduria, type I, 250950 (3), Autosomal recessive"	Auh (MGI:1338011)			
chr9	91409044	91425062	9q22.1-q22.3	9q22.31		605327	"NFIL3, NFIL3A, E4BP4"	"Nuclear factor, interleukin 3-regulated"	NFIL3	4783	ENSG00000165030			Nfil3 (MGI:109495)			
chr9	91722595	91950205	9q22	9q22.31		602337	"ROR2, BDB1, BDB, NTRKR2"	Receptor tyrosine kinase-like orphan receptor 2	ROR2	4920	ENSG00000169071		"Brachydactyly, type B1, 113000 (3), Autosomal dominant; Robinow syndrome, autosomal recessive, 268310 (3), Autosomal recessive"	Ror2 (MGI:1347521)			
chr9	92031133	92115473	9q22.1-q22.3	9q22.31		605712	"SPTLC1, LBC1, SPT1, HSN1, HSAN"	"Serine palmitoyltransferase, long-chain base subunit 1"	SPTLC1	10558	ENSG00000090054		"Neuropathy, hereditary sensory and autonomic, type IA, 162400 (3), Autosomal dominant"	Sptlc1 (MGI:1099431)			
chr9	92210206	92293755	9q21	9q22.31		600709	"IARS, GRIDHH"	Isoleucine-tRNA synthetase	IARS	3376	ENSG00000196305		"Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy, 617093 (3), Autosomal recessive"	Iars (MGI:2145219)			
chr9	92297357	92325993	9q22.32	9q22.31		611534	"NOL8, NOP132"	Nucleolar protein 8	NOL8	55035	ENSG00000198000			Nol8 (MGI:1918180)			
chr9	92325456	92615163	9q22.31	9q22.31		611505	CENPP	Centromeric protein P	CENPP	401541	ENSG00000188312			Cenpp (MGI:1913586)			
chr9	92383270	92404698	9q22.3	9q22.31		602383	"OGN, OIF"	Osteoglycin	OGN	4969	ENSG00000106809			Ogn (MGI:109278)			
chr9	92456204	92482561	9q21.3-q22	9q22.31		608135	"ASPN, PLAP1, OS3"	Asporin	ASPN	54829	ENSG00000106819		"{Lumbar disc degeneration}, 603932 (3); {Osteoarthritis susceptibility 3}, 607850 (3), Autosomal dominant"	Aspn (MGI:1913945)			
chr9	92493546	92536840	9q22.3	9q22.31		603479	ECM2	Extracellular matrix protein-2	ECM2	1842	ENSG00000106823			Ecm2 (MGI:3039578)			
chr9	92711362	92764840	9q22.3	9q22.31		609797	"BICD2, KIAA0699, SMALED2"	"Bicaudal D, Drosophila, homolog of, 2"	BICD2	23299	ENSG00000185963		"Spinal muscular atrophy, lower extremity-predominant, 2, AD, 615290 (3), Autosomal dominant"	Bicd2 (MGI:1924145)			
chr9	92947318	93036235	9q22.31	9q22.31		617554	"FGD3, ZFYVE5"	"FYVE, RhoGEF, and Ph domain-containing protein 3"	FGD3	89846	ENSG00000127084			Fgd3 (MGI:1353657)			
chr9	93058687	93085137	9q22.31	9q22.31		616429	SUSD3	SUSHI domain-containing protein 3	SUSD3	203328	ENSG00000157303			Susd3 (MGI:1913579)			
chr9	93096122	93113294	9q22.32	9q22.31		617726	"CARD19, BINCARD, C9orf89"	Caspase recruitment domain-containing protein 19	CARD19	84270	ENSG00000165233			Card19 (MGI:1915730)			
chr9	93121488	93134303	9q22	9q22.31		602062	NINJ1	Ninjurin	NINJ1	4814	ENSG00000131669			Ninj1 (MGI:1196617)			
chr9	93184155	93327580	9q22.3	9q22.31		606249	"WNK2, PRKWNK2"	WNK lysine deficient protein kinase 2	WNK2	65268	ENSG00000165238			Wnk2 (MGI:1922857)			
chr9	93451695	93566114	9q22.31	9q22.31		612265	"FAM120A, C9orf10, KIAA0183"	"Family with sequence similarity 120, member A"	FAM120A	23196	ENSG00000048828			Fam120a (MGI:2446163)			
chr9	93576626	93679586	9q22	9q22.31		604351	PHF2	PHD finger protein-2	PHF2	5253	ENSG00000197724			Phf2 (MGI:1338034)			
chr9	93951626	93955325	9q12	9q22.32		603260	BARX1	BarH-like homeo box gene 1	BARX1	56033	ENSG00000131668			Barx1 (MGI:103124)			
chr9	94175956	94176035	9q22.32	9q22.32		605386	"MIRLET7A1, LET7A1, MIRNLET7A1"	Micro RNA Let7a1	MIRLET7A1	406881							
chr9	94176346	94176432	9q22.32	9q22.32		612146	"MIRLET7F1, LET7F1, MIRNLET7F1"	Micro RNA Let7f1	MIRLET7F1	406888							
chr9	94178833	94178919	9q22.32	9q22.32		612145	"MIRLET7D, LET7D, MIRNLET7D"	Micro RNA Let7d	MIRLET7D	406886							
chr9	94259265	94303966	9q22.3	9q22.32		603404	ZNF169	Zinc finger protein-169	ZNF169	169841	ENSG00000175787			Zfp169 (MGI:1915161)			
chr9	94558713	94593831	Chr.9	9q22.32		603027	FBP2	"Fructose-1,6-bisphosphatase 2"	FBP2	8789	ENSG00000130957			Fbp2 (MGI:95491)			
chr9	94603132	94640257	9q22.2-q22.3	9q22.32		611570	FBP1	Fructose-bisphosphatase 1	FBP1	2203	ENSG00000165140		"Fructose-1,6-bisphosphatase deficiency, 229700 (3), Autosomal recessive"	Fbp1 (MGI:95492)			
chr9	95085207	95085303	9q22.32	9q22.32		610723	"MIR23B, MIRN23B"	Micro RNA 23B	MIR23B	407011							
chr9	95085444	95085540	9q22.32	9q22.32		610636	"MIR27B, MIRN27B"	Micro RNA 27B	MIR27B	407019							
chr9	95086020	95086087	9q22.32	9q22.32		609705	"MIR189, MIRN24-1"	Micro RNA 24-1	MIR24-1	407012							
chr9	95099053	95317729	9q22.3	9q22.32		613899	"FANCC, FACC"	"Fanconi anemia, complementation group C"	FANCC	2176	ENSG00000158169		"Fanconi anemia, complementation group C, 227645 (3), Autosomal recessive"	Fancc (MGI:95480)			
chr9	95442979	95517056	9q22.3	9q22.32		601309	"PTCH1, NBCCS, BCNS, HPE7"	"Patched, Drosophila, homolog of"	PTCH1	5727	ENSG00000185920		"Basal cell carcinoma, somatic, 605462 (3); Basal cell nevus syndrome, 109400 (3), Autosomal dominant; Holoprosencephaly 7, 610828 (3), Autosomal dominant"	Ptch1 (MGI:105373)			
chr9	95875617	96041091	9q22.32	9q22.32		615667	"ERCC6L2, RAD26L, BMFS2"	ERCC6-like 2	ERCC6L2	375748	ENSG00000182150		"Bone marrow failure syndrome 2, 615715 (3), Autosomal recessive"	Ercc6l2 (MGI:1923501)			
chr9	96235305	96313986	9q22	9q22.32		605573	"HSD17B3, EDH17B3"	Hydroxysteroid (17-beta) dehydrogenase 3	HSD17B3	3293	ENSG00000130948		"Pseudohermaphroditism, male, with gynecomastia, 264300 (3), Autosomal recessive"	Hsd17b3 (MGI:107177)			
chr9	96313436	96383709	9q22.3	9q22.32		609182	"SLC35D2, HFRC1, SQV7L"	"Solute carrier family 35, member D2"	SLC35D2	11046	ENSG00000130958			Slc35d2 (MGI:1917734)			
chr9	96385940	96418638	9q22.32	9q22.32		610160	"ZNF367, AFF29"	Zinc finger protein 367	ZNF367	195828	ENSG00000165244			Zfp367 (MGI:2442266)			
chr9	96492742	96619829	9q22.32-q22.33	9q22.32-q22.33		603505	CDC14B	"Cell division cycle 14, S. cerevisiae, homolog B"	CDC14B	8555	ENSG00000081377			Cdc14b (MGI:2441808)			
chr9	97029676	97039642	9q22.2	9q22.33		603308	"CTSL2, CTSV"	Cathepsin L2	CTSV	1515	ENSG00000136943			Ctsl (MGI:88564)			
chr9	97412019	97496124	9q22.33	9q22.33		611258	"TDRD7, KIAA1529, TRAP, CATC4, CTRCT36"	Tudor domain-containing protein 7	TDRD7	23424	ENSG00000196116		"Cataract 36, 613887 (3), Autosomal recessive"	Tdrd7 (MGI:2140279)			
chr9	97501179	97601742	9q22.3	9q22.33		190930	TMOD	Tropomodulin	TMOD1	7111	ENSG00000136842			Tmod1 (MGI:98775)			
chr9	97633422	97673747	9q22.3-q31	9q22.33		600469	NCBP1	"Nuclear cap binding protein 1, 80kD"	NCBP1	4686	ENSG00000136937	in 500kb of XPA		Ncbp1 (MGI:1891840)			
chr9	97654397	97697408	9q22.3	9q22.33		611153	"XPA, XPAC"	XPA complementing gene	XPA	7507	ENSG00000136936		"Xeroderma pigmentosum, group A, 278700 (3), Autosomal recessive"	Xpa (MGI:99135)			
chr9	97853254	97856714	9q22	9q22.33		602617	"FOXE1, FKHL15, TITF2, TTF2, NMTC4"	Forkhead box E1 (thyroid transcription factor-2)	FOXE1	2304	ENSG00000178919		"Bamforth-Lazarus syndrome, 241850 (3), Autosomal recessive; {Thyroid cancer, nonmedullary, 4}, 616534 (3), Autosomal dominant"	Foxe1 (MGI:1353500)			
chr9	97926790	97944914	9q22	9q22.33		610715	"HEMGN, EDAG"	Hemogen	HEMGN	55363	ENSG00000136929			Hemgn (MGI:2136910)			
chr9	98056676	98083082	9q22.33	9q22.33		605202	"NANS, SAS, SEMDCG"	N-acetylneuraminic acid synthase (sialic acid synthase)	NANS	54187	ENSG00000095380		"Spondyloepimetaphyseal dysplasia, Camera-Genevieve type, 610442 (3), Autosomal recessive"	Nans (MGI:2149820)			
chr9	98072013	98119419	9q22-q31	9q22.33		606556	"TRIM14, KIAA0129"	Tripartite motif-containing protein 14	TRIM14	9830	ENSG00000106785			Trim14 (MGI:1921985)			
chr9	98120974	98192673	9q22.3	9q22.33		602159	"CORO2A, WDR2, IR10"	Coronin 2A	CORO2A	7464	ENSG00000106789			Coro2a (MGI:1345966)			
chr9	98198997	98255720	9q22.3	9q22.33		609871	"TBC1D2, PARIS1"	"TBC1 domain family, member 2"	TBC1D2	55357	ENSG00000095383			Tbc1d2 (MGI:2652885)			
chr9	98288081	98709196	9q22.1	9q22.33		607340	"GABBR2, GPR51, EIEE59, NDPLHS"	Gamma-aminobutyric acid B receptor 2	GABBR2	9568	ENSG00000136928		"Epileptic encephalopathy, early infantile, 59, 617904 (3), Autosomal dominant; Neurodevelopmental disorder with poor language and loss of hand skills, 617903 (3), Autosomal dominant; {Nicotine dependence, protection against}, 188890 (3); {Nicotine dependence, susceptibility to}, 188890 (3)"	Gabbr2 (MGI:2386030)			
chr9	98732008	98796541	9q22.33	9q22.33		615370	"ANKS6, PKDR1, NPHP16"	Ankyrin repeat and sterile alpha motif domains-containing protein 6	ANKS6	203286	ENSG00000165138		"Nephronophthisis 16, 615382 (3), Autosomal recessive"	Anks6 (MGI:1922941)			
chr9	98807698	98850080	9q22	9q22.33		610290	"GALNT12, CRCS1"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 12	GALNT12	79695	ENSG00000119514		"{Colorectal cancer, susceptibility to, 1}, 608812 (3)"	Galnt12 (MGI:2444664)			
chr9	98943391	99070791	9q21-q22	9q22.33		120325	COL15A1	"Collagen XV, alpha-1 polypeptide"	COL15A1	1306	ENSG00000204291			Col15a1 (MGI:88449)			
chr9	99104037	99154191	9q22	9q22.33		190181	"TGFBR1, ALK5, AAT5, LDS1, MSSE"	"Transforming growth factor, beta receptor I (activin A receptor type II-like kinase, 53kD)"	TGFBR1	7046	ENSG00000106799		"Loeys-Dietz syndrome 1, 609192 (3), Autosomal dominant; {Multiple self-healing squamous epithelioma, susceptibility to}, 132800 (3), Autosomal dominant"	Tgfbr1 (MGI:98728)			
chr9	99216424	99221963	9q22	9q22.33		607905	"ALG2, CDGII, CMSTA3, CMS14"	"Alg2, S. cerevisiae, homolog of"	ALG2	85365	ENSG00000119523	mutation identified in 1 CDGII patient	"?Congenital disorder of glycosylation, type Ii, 607906 (3), Autosomal recessive; Myasthenic syndrome, congenital, 14, with tubular aggregates, 616228 (3), Autosomal recessive"	Alg2 (MGI:1914731)			
chr9	99222287	99230618	9q22.33	9q22.33		609214	SEC61B	"Sec61 complex, beta subunit"	SEC61B	10952	ENSG00000106803			Sec61b (MGI:1913462)			
chr9	99800000	105400000	9q31.1			614954	CHDT3	"Congenital heart defects, multiple types, 3"		101154642		max lod at D9S1690	"Congenital heart defects, multiple types, 3, 614954 (2), Autosomal dominant"				
chr9	99800000	114900000	9q31-q32			608026	HNP1	Hypertensive nephropathy		574045			"Hypertensive nephropathy, 608026 (2)"				
chr9	99800000	112100000	9q31			600156	HSCR5	"Hirschsprung disease, susceptibility to, 5"		404720			"{Hirschsprung disease, susceptibility to, 5}, 600156 (2), Autosomal dominant"				
chr9	99800000	112100000	9q31			607853	PAND2	Panic disorder 2		619493		max lod at D9S271	"Panic disorder 2, 607853 (2)"				
chr9	99800000	138394717	9q31-q34			183840	SPDA2	"Spondyloarthropathy, susceptibility to, 2"		791255		max lod at D9S1776	"{Spondyloarthropathy, susceptibility to, 2}, 183840 (2), Autosomal dominant"				
chr9	99821854	99866892	9q22	9q31.1		600542	CSMF	"Chondrosarcoma, extraskeletal myxoid, fused to EWS in"	NR4A3	8013	ENSG00000119508	t(9;17)(q22;q11); t(9;22)(q22;q11-q12)	"Chondrosarcoma, extraskeletal myxoid, 612237 (3)"	Nr4a3 (MGI:1352457)			
chr9	99906632	99974540	9q31	9q31.1		604204	STX17	Syntaxin 17	STX17	55014	ENSG00000136874			Stx17 (MGI:1914977)			
chr9	99979178	100099051	9q31.1	9q31.1		609170	"TXNDC4, KIAA0573"	Thioredoxin domain-containing protein 4	ERP44	23071	ENSG00000023318			Erp44 (MGI:1923549)			
chr9	100099184	100302174	9q31	9q31.1		243305	"INVS, INV, NPHP2, NPH2"	Inversin	INVS	27130	ENSG00000119509		"Nephronophthisis 2, infantile, 602088 (3), Autosomal recessive"	Invs (MGI:1335082)			
chr9	100302074	100352976	9q31.1	9q31.1		616717	TEX10	Testis-expressed gene 10	TEX10	54881	ENSG00000136891			Tex10 (MGI:1344413)			
chr9	100473237	100577635	9q31	9q31.1		603421	"TMEFF1, C9orf2"	Transmembrane protein with EGF-like and 2 follistatin-like domains 1	TMEFF1	8577	ENSG00000241697			Tmeff1 (MGI:1926810)			
chr9	100578078	100588388	9q31	9q31.1		617714	"CAVIN4, MURC"	Caveolae-associated protein 4	CAVIN4	347273	ENSG00000170681			Cavin4 (MGI:1915266)			
chr9	101360416	101385004	9q22.3	9q31.1		602938	BAAT	Bile acid coenzyme A:amino acid N-acyltransferase (glycine N-choloyltransferase)	BAAT	570	ENSG00000136881		"Hypercholanemia, familial, 607748 (3)"	Baat (MGI:106642)			
chr9	101389966	101398636	9q31.1	9q31.1		611854	MRPL50	Mitochondrial ribosomal protein L50	MRPL50	54534	ENSG00000136897	"pseudogenes on 2, 5, and 10"		Mrpl50 (MGI:107329)			
chr9	101398829	101410659	9q22-q31	9q31.1		603132	ZNF189	Zinc finger protein-189	ZNF189	7743	ENSG00000136870			Zfp189 (MGI:2444707)			
chr9	101420559	101435779	9q22.3	9q31.1		612724	ALDOB	"Aldolase B, fructose-bisphosphatase"	ALDOB	229	ENSG00000136872		"Fructose intolerance, hereditary, 229600 (3), Autosomal recessive"	Aldob (MGI:87995)			
chr9	101533848	101563343	9q31.1	9q31.1		607699	"RNF20, BRE1A"	Ring finger protein 20	RNF20	56254	ENSG00000155827			Rnf20 (MGI:1925927)			
chr9	101569351	101738579	9q31.1	9q31.1		606650	"GRIN3A, NR3A"	"Glutamate receptor, ionotropic, N-methyl-D-aspartate 3A"	GRIN3A	116443	ENSG00000198785			Grin3a (MGI:1933206)			
chr9	101591614	101595000	9q31.1	9q31.1		613821	"PPP3R2, PPP3RL, CBLP"	"Protein phosphatase 3, regulatory subunit B, beta"	PPP3R2	5535	ENSG00000188386			Ppp3r2 (MGI:107171)			
chr9	102995310	103018487	9q31.1	9q31.1		604035	CYLC2	Cylicin 2	CYLC2	1539	ENSG00000155833						
chr9	104093759	104141418	Chr.9	9q31.1		605576	CAPE	Chromosome-associated protein E	SMC2	10592	ENSG00000136824			Smc2 (MGI:106067)			
chr9	104747567	104760123	9q31.1	9q31.1		608871	"NIPSNAP3A, TASSC"	"NIPSNAP, C. elegans, homolog of, 3A"	NIPSNAP3A	25934	ENSG00000136783			Nipsnap3b (MGI:1913786)			
chr9	104781001	104928245	9q22-q31	9q31.1		600046	"ABCA1, ABC1, HDLDT1, TGD"	ATP-binding cassette 1	ABCA1	19	ENSG00000165029		"{Coronary artery disease in familial hypercholesterolemia, protection against}, 143890 (3), Autosomal dominant; HDL deficiency, type 2, 604091 (3); Tangier disease, 205400 (3), Autosomal recessive"	Abca1 (MGI:99607)			
chr9	105244604	105439774	9q31.2	9q31.1-q31.2		606105	"SLC44A1, CTL1, CDW92"	"Solute carrier family 44, member 1"	SLC44A1	23446	ENSG00000070214			Slc44a1 (MGI:2140592)			
chr9	105400000	134500000	9q31.2-q34.2			612238	IS4	"Scoliosis, idiopathic, susceptibility to, 4"		100190785		max lod at D9S2157	"{Scoliosis, idiopathic, susceptibility to, 4}, 612238 (2)"				
chr9	105400000	108500000	9q31.2			612883	MENAQ3	"Menarche, age at, QTL3"		100302563		associated with rs2090409	"{Menarche, age at, QTL3}, 612883 (2)"				
chr9	105442182	105552432	9q31	9q31.2		609829	"FSD1NL, FSD1L, MIR1, CCDC10"	FSD1 N-terminus-like protein	FSD1L	83856	ENSG00000106701			Fsd1l (MGI:2442443)			
chr9	105558116	105655949	9q31	9q31.2		607440	"FKTN, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4"	Fukutin	FKTN	2218	ENSG00000106692		"Cardiomyopathy, dilated, 1X, 611615 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4, 253800 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4, 613152 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4, 611588 (3), Autosomal recessive"	Fktn (MGI:2179507)			
chr9	105662456	105663111	9q31	9q31.2		186855	TAL2	T-cell acute lymphocytic leukemia-2	TAL2	6887	ENSG00000186051	33kb from breakpoint in t(7;9)	"Leukemia, T-cell acute lymphocytic, somatic, 613065 (3)"	Tal2 (MGI:99540)			
chr9	105694524	105776610	9q31.2	9q31.2		611236	"TMEM38B, TRICB, OI14"	Transmembrane protein 38B	TMEM38B	55151	ENSG00000095209		"Osteogenesis imperfecta, type XIV, 615066 (3)"	Tmem38b (MGI:1098718)			
chr9	106860153	107013633	9q31.2	9q31.2		617371	"ZNF462, KIAA1803"	Zinc finger protein 462	ZNF462	58499	ENSG00000148143			Zfp462 (MGI:107690)			
chr9	107283235	107332193	9q31.2	9q31.2		600062	RAD23B	"RAD23 (Saccharomyces cerevisiae) homolog of, B"	RAD23B	5887	ENSG00000119318	previously 3p25.1		Rad23b (MGI:105128)			
chr9	107484851	107489719	9q31	9q31.2		602253	"KLF4, EZF, GKLF"	Kruppel-like factor 4	KLF4	9314	ENSG00000136826			Klf4 (MGI:1342287)			
chr9	108854587	108855994	9q31	9q31.3		604304	ACTL7B	Actin-like 7B	ACTL7B	10880	ENSG00000148156			Actl7b (MGI:1343053)			
chr9	108862227	108863754	9q31	9q31.3		604303	ACTL7A	Actin-like 7A	ACTL7A	10881	ENSG00000187003			Actl7a (MGI:1343051)			
chr9	108867516	108934331	9q31	9q31.3		603722	"IKBKAP, IKAP"	"Inhibitor of kappa light polypeptide gene enhancer in B cells, kinase complex-associated protein"	ELP1	8518	ENSG00000070061		"Dysautonomia, familial, 223900 (3), Autosomal recessive"	Ikbkap (MGI:1914544)			
chr9	108942568	109013593	9q31.2	9q31.3		604785	CTNNAL1	"Catenin, alpha-like, 1"	CTNNAL1	8727	ENSG00000119326			Ctnnal1 (MGI:1859649)			
chr9	109046228	109046297	9q31.3	9q31.3		609355	"MIR32, MIRN32"	Micro RNA 32	MIR32	407036							
chr9	109130292	109167290	9q31.3	9q31.3		604574	"FRRS1L, C9orf4, CG6, EIEE37"	Ferric-chelate reductase 1-like	FRRS1L	23732	ENSG00000260230		"Epileptic encephalopathy, early infantile, 37, 616981 (3), Autosomal recessive"	Frrs1l (MGI:2442704)			
chr9	109171973	109320963	9q31-q32	9q31.3		610340	"EPB41L4B, EHM2"	Erythrocyte membrane protein band 4.1-like 4B	EPB41L4B	54566	ENSG00000095203			Epb41l4b (MGI:1859149)			
chr9	109375693	109538394	9q31.3	9q31.3		176877	"PTPN3, PTPH1"	"Protein-tyrosine phosphatase, nonreceptor-type, 3"	PTPN3	5774	ENSG00000070159			Ptpn3 (MGI:105307)			
chr9	110048597	110172511	9q31-q33	9q31.3		604582	"AKAP2, AKAPKL, KIAA0920, PALM2"	A-kinase anchor protein 2	AKAP2	11217	ENSG00000241978	multiple splice variants		Akap2 (MGI:1306795)			
chr9	110243811	110256639	9q31	9q31.3		187700	TXN	Thioredoxin	TXN	7295	ENSG00000136810	incorrectly assigned to 3		Txn1 (MGI:98874)			
chr9	110300899	110337886	9q32	9q31.3		617789	"TXNDC8, SPTRX3"	Thioredoxin domain-containing protein 8	TXNDC8	255220	ENSG00000204193			Txndc8 (MGI:1914652)			
chr9	110365247	110579879	9q32	9q31.3		611691	"SVEP1, POLYDOM, SELOB"	"Sushi, von willebrand factor type A, EGF, and pentraxin domain-containing 1"	SVEP1	79987	ENSG00000165124			Svep1 (MGI:1928849)			
chr9	110668188	110806632	9q31.3-q32	9q31.3		601296	"MUSK, CMS9, FADS"	Receptor tyrosine kinase MuSK	MUSK	4593	ENSG00000030304		"Fetal akinesia deformation sequence, 208150 (3), Autosomal recessive; Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency, 616325 (3), Autosomal recessive"	Musk (MGI:103581)			
chr9	110873251	111039258	9q31.3	9q31.3		602282	"LPAR1, EDG2, LPA1, VZG1"	Lysophosphatidic acid receptor 1	LPAR1	1902	ENSG00000198121			Lpar1 (MGI:108429)			
chr9	111360692	111484744	9q31.3	9q31.3		616694	"KIAA0368, ECM29"	KIAA0368 gene	ECPAS	23392	ENSG00000136813			AI314180 (MGI:2140220)			
chr9	111549721	111599854	9q31.3	9q31.3		601274	"PTGR1, LTB4DH"	Prostaglandin reductase 1	PTGR1	22949	ENSG00000106853			Ptgr1 (MGI:1914353)			
chr9	111661570	111670245	9q31.3	9q31.3		604389	GNG10	"Guanine nucleotide-binding protein, gamma 10"	GNG10	2790	ENSG00000242616			Gng10 (MGI:1336169)			
chr9	111896765	111935373	9q31	9q31.3		602874	"UGCG, GCS"	UDP-glucose ceramide glucosyltransferase	UGCG	7357	ENSG00000148154			Ugcg (MGI:1332243)			
chr9	112100000	127500000	9q32-q33			611488	ARMD10	"Macular degeneration, age-related, 10"		107880065			"Macular degeneration, age-related, 10, 611488 (2)"				
chr9	112100000	127500000	9q32-q33			608762	EIG3	"Epilepsy, idiopathic generalized, susceptibility to 3"		432400			"{Epilepsy, idiopathic generalized, susceptibility to, 3}, 608762 (2), Autosomal recessive"				
chr9	112100000	114900000	9q32			612259	IBD16	"Inflammatory bowel disease 16, susceptibility to"		100190930			"{Inflammatory bowel disease 16}, 612259 (2)"				
chr9	112217714	112333668	Chr.9	9q32		607527	ROD1	Regulator of differentiation 1	PTBP3	9991	ENSG00000119314			Ptbp3 (MGI:1923334)			
chr9	112486967	112665310	3q32	9q32		617390	KIAA1958	KIAA1958 gene	KIAA1958	158405	ENSG00000165185						
chr9	112683947	112718148	9q32	9q32		613273	"INIP, C9orf80, SOSSC"	INST3- and NABP-interacting protein	INIP	58493	ENSG00000148153			Inip (MGI:1913459)			
chr9	112878919	112895537	9q31-q34	9q32		608956	"SLC46A2, TSCOT"	"Solute carrier family 46, member 2"	SLC46A2	57864	ENSG00000119457			Slc46a2 (MGI:1353616)			
chr9	113041814	113056790	9q32	9q32		602951	ZFP37	"Zinc finger protein-37, mouse, homolog of"	ZFP37	7539	ENSG00000136866	?candidate for Nager syndrome		Zfp37 (MGI:99181)			
chr9	113150957	113164141	9q31-q32	9q32		603088	"SLC13A2, COPT2, CTR2"	"Solute carrier family 31 (copper transporter), member 2"	SLC31A2	1318	ENSG00000136867			Slc31a2 (MGI:1333844)			
chr9	113165035	113221360	9q32	9q32		617398	"FKBP15, FKBP133, KIAA0674, WAFL"	FK506-binding protein 15	FKBP15	23307	ENSG00000119321			Fkbp15 (MGI:2444782)			
chr9	113221527	113264491	9q31-q32	9q32		603085	"SLC31A1, COPT1, CTR1"	"Solute carrier family 31 (copper transporter), member 1"	SLC31A1	1317	ENSG00000136868			Slc31a1 (MGI:1333843)			
chr9	113267007	113275588	9q32	9q32		614533	"CDC26, APC12"	"Cell division cycle 26, S. cerevisiae, homolog of"	CDC26	246184	ENSG00000176386	pseudogene on 7q32.1		Cdc26 (MGI:1913690)			
chr9	113275633	113292904	9q31-q33	9q32		607795	"PRPF4, PRP4, HPRP4, RP70"	"Precursor mRNA-processing factor 4, S. cerevisiae, homolog of"	PRPF4	9128	ENSG00000136875		"Retinitis pigmentosa 70, 615922 (3), Autosomal dominant"	Prpf4 (MGI:1917302)			
chr9	113386311	113401337	9q34	9q32		125270	"ALAD, ALADH, PBGS"	"Aminolevulinate, delta-, dehydratase"	ALAD	210	ENSG00000148218	linked to ABO; ORM-ALAD-AK-ABO	"{Lead poisoning, susceptibility to}, 612740 (3), Autosomal recessive; Porphyria, acute hepatic, 612740 (3), Autosomal recessive"	Alad (MGI:96853)			
chr9	113407234	113410748	9q33	9q32		607267	"POLE3, CHARAC17, YBL1"	"Polymerase, DNA, epsilon-3"	POLE3	54107	ENSG00000148229			Pole3 (MGI:1933378)			
chr9	113444031	113597742	9q31-q33	9q32		602189	RGS3	Regulator of G-protein signaling-3	RGS3	5998	ENSG00000138835			Rgs3 (MGI:1354734)			
chr9	113876281	114056594	9q32	9q32		617077	"ZNF618, NEDD10, KIAA1952"	Zinc finger protein 618	ZNF618	114991	ENSG00000157657			Zfp618 (MGI:1919950)			
chr9	114060126	114078471	9q32-q33	9q32		176870	"AMBP, ITIL, ITI, HCP"	"Alpha-1-microglobulin/bikunin precursor (inter-alpha-trypsin inhibitor, light chain; protein HC)"	AMBP	259	ENSG00000106927			Ambp (MGI:88002)			
chr9	114091622	114100089	9q32	9q32		611278	KIF12	Kinesin family member 12	KIF12	113220	ENSG00000136883			Kif12 (MGI:1098232)			
chr9	114154270	114312515	9q32	9q32		608461	"COL27A1, KIAA1870, STLS"	"Collagen, type XXVII, alpha-1"	COL27A1	85301	ENSG00000196739	mutation identified in 1 STLS family	"?Steel syndrome, 615155 (3), Autosomal recessive"	Col27a1 (MGI:2672118)			
chr9	114323022	114326478	9q34.1-q34.3	9q32		138600	"ORM1, AGP1"	Orosomucoid-1 (alpha-1-acid glycoprotein-1)	ORM1	5004	ENSG00000229314	"linked to ABO, AK1, ALAD"					
chr9	114329788	114333255	9q34.1-q34.3	9q32		138610	ORM2	Orosomucoid-2	ORM2	5005	ENSG00000228278						
chr9	114402077	114505499	9q32-q34	9q32		607928	"WHRN, CIP98, KIAA1526, DFNB31, USH2D"	Whirlin	WHRN	25861	ENSG00000095397		"Deafness, autosomal recessive 31, 607084 (3), Autosomal recessive; Usher syndrome, type 2D, 611383 (3), Autosomal recessive"	Whrn (MGI:2682003)			
chr9	114587713	114598871	Chr.9	9q32		607296	"ATP6V1G1, ATP6G1"	"ATPase, H+ transporting, lysosomal, 13kD, V1 subunit G, isoform 1"	ATP6V1G1	9550	ENSG00000136888			Atp6v1g1 (MGI:1913540)			
chr9	114784634	114806127	9q32	9q32		604052	"TNFSF15, TL1, VEGI"	"Tumor necrosis factor ligand superfamily, member 15 (vascular endothelial growth inhibitor)"	TNFSF15	9966	ENSG00000181634			Tnfsf15 (MGI:2180140)			
chr9	114893342	114930673	9q33	9q32-q33		603875	"TNFSF8, CD30L, CD30LG"	"Tumor necrosis factor ligand superfamily, member 8 (CD30 ligand)"	TNFSF8	944	ENSG00000106952			Tnfsf8 (MGI:88328)			
chr9	114900000	127500000	9q33			613207	ASRT8	"Asthma-related traits, susceptibility to, 8"		100415896		associated with rs3789873	"{Asthma-related traits, susceptibility to, 8}, 613207 (2)"				
chr9	115019574	115118256	9q33	9q33.1		187380	"TNC, HXB, DFNA56"	Tenascin C (hexabrachion)	TNC	3371	ENSG00000041982	proximal to ABL	"Deafness, autosomal dominant 56, 615629 (3), Autosomal dominant"	Tnc (MGI:101922)			
chr9	115141817	115402643	9q32	9q33.1		604767	1-Dec	Deleted in esophageal cancer 1	1-Dec	50514	ENSG00000173077		"Esophageal squamous cell carcinoma, 133239 (1), Autosomal dominant"				
chr9	116153751	116402320	9q33.1	9q33.1		176385	PAPPA	Pregnancy-associated plasma protein A	PAPPA	5069	ENSG00000182752			Pappa (MGI:97479)			
chr9	116398156	116400605	9q33.1	9q33.1		610689	DIPAS	"DIPLA1, antisense"	PAPPA-AS1	493913							
chr9	116425224	117415038	9q33.1	9q33.1		612856	"ASTN2, KIAA0634"	Astrotactin 2	ASTN2	23245	ENSG00000148219			Astn2 (MGI:1889277)			
chr9	116687301	116701299	9q31-q34.1	9q33.1		602290	"TRIM32, HT2A, LGMD2H, BBS11"	Tripartite-motif-containing protein 32	TRIM32	22954	ENSG00000119401	mutation identified in 1 BBS11 family	"?Bardet-Biedl syndrome 11, 615988 (3), Autosomal recessive; Muscular dystrophy, limb-girdle, type 2H, 254110 (3), Autosomal recessive"	Trim32 (MGI:1917057)			
chr9	117704174	117717490	9q32-q33	9q33.1		603030	TLR4	Toll-like receptor-4	TLR4	7099	ENSG00000136869			Tlr4 (MGI:96824)			
chr9	119166629	119369460	9q33.1	9q33.1		602865	"BRINP1, DBC1, DBCCR1"	Bone morphogenetic protein/retinoic acid-inducible neural-specific protein 1	BRINP1	1620	ENSG00000078725			Brinp1 (MGI:1928478)			
chr9	120388868	120580169	9q33.3	9q33.2		608201	"CDK5RAP2, KIAA1633, MCPH3"	CDK5 regulatory subunit-associated protein 2	CDK5RAP2	55755	ENSG00000136861		"Microcephaly 3, primary, autosomal recessive, 604804 (3), Autosomal recessive"	Cdk5rap2 (MGI:2384875)			
chr9	120600917	120714486	9q32-q33.3	9q33.2		604268	"MEGF9, EGFL5"	Multiple epidermal growth factor-like domains 9	MEGF9	1955	ENSG00000106780			Megf9 (MGI:1918264)			
chr9	120756975	120793461	9q34	9q33.2		609071	"FBXW2, FBW2, FWD2"	F-box and WD40 domain protein 2	FBXW2	26190	ENSG00000119402			Fbxw2 (MGI:1353435)			
chr9	120816052	120843020	9q33.2	9q33.2		604452	"PSMD5, S5B"	"Proteasome 26S subunit, non-ATPase, 5"	PSMD5	5711	ENSG00000095261			Psmd5 (MGI:1914248)			
chr9	120855650	120902159	9q33.3	9q33.2		609740	PHF19	PHD finger protein 19	PHF19	26147	ENSG00000119403			Phf19 (MGI:1921266)			
chr9	120902392	120929172	9q33-q34	9q33.2		601711	TRAF1	TNF receptor-associated factor 2	TRAF1	7185	ENSG00000056558			Traf1 (MGI:101836)			
chr9	120952334	121075173	9q34.1	9q33.2		120900	"C5, C5D, ECLZB"	Complement component-5	C5	727	ENSG00000106804		"C5 deficiency, 609536 (3); [Eculizumab, poor response to], 615749 (3), Autosomal dominant"	Hc (MGI:96031)			
chr9	121074772	121177609	9q33	9q33.2		605496	"CEP1, CEP110, FAN"	Centrosomal protein 1	CNTRL	11064	ENSG00000119397			Cntrl (MGI:1889576)			
chr9	121178136	121202086	9q33.2	9q33.2		612673	RAB14	Ras-associated protein	RAB14	51552	ENSG00000119396			Rab14 (MGI:1915615)			
chr9	121201482	121332843	9q34	9q33.2		137350	GSN	Gelsolin	GSN	2934	ENSG00000148180	40kb proximal to ABL	"Amyloidosis, Finnish type, 105120 (3), Autosomal dominant"	Gsn (MGI:95851)			
chr9	121338987	121370303	9q34.1	9q33.2		133090	"STOM, EPB72, BND7"	Stomatin (erythrocyte membrane protein band 7.2)	STOM	2040	ENSG00000148175	proximal to ABL		Stom (MGI:95403)			
chr9	121455040	121500026	9q33-q34	9q33.2		104175	"GGTA1P, GGTA1"	"Glycoprotein, alpha-galactosyltransferase-1 pseudogene"	GGTA1P	2681		processed pseudogene GGTA1P on 12q14-q15					
chr9	121566882	121785529	9q33	9q33.2		609205	"DAB2IP, AIP1, KIAA1743"	DAB2-interacting protein	DAB2IP	153090	ENSG00000136848			Dab2ip (MGI:1916851)			
chr9	122132465	122159818	9q33.2-q34.11	9q33.2		603359	NDUFA8	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 8"	NDUFA8	4702	ENSG00000119421			Ndufa8 (MGI:1915625)			
chr9	122185625	122228892	9q33.2	9q33.2		608215	LHX6	LIM homeobox gene 6	LHX6	26468	ENSG00000106852			Lhx6 (MGI:1306803)			
chr9	122264602	122325314	9q32-q34.1	9q33.2		604602	"MRFF, RRF"	"Ribosome-recycling factor, mitochondrial"	MRRF	92399	ENSG00000148187			Mrrf (MGI:1915121)			
chr9	122369905	122395702	9q32-q33.3	9q33.2		176805	"PTGS1, COX1, PGHS1, COX3, PCOX1"	Prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)	PTGS1	5742	ENSG00000095303			Ptgs1 (MGI:97797)			
chr9	122816057	122828655	Chr.9	9q33.2		604421	PDCL	Phosducin-like	PDCL	5082	ENSG00000136940			Pdcl (MGI:1914716)			
chr9	122844564	122905350	9q34	9q33.2		615231	"RC3H2, MNAB"	RING finger and CCCH-type zinc finger domains-containing protein 2	RC3H2	54542	ENSG00000056586			Rc3h2 (MGI:2442789)			
chr9	122931639	123104868	9q33.2-q33.3	9q33.2-q33.3		615882	"RABGAP1, GAPCENA, TBC1D11"	RAB GTPase-activating protein 1	RABGAP1	23637	ENSG00000011454			Rabgap1 (MGI:2385139)			
chr9	123033634	123042750	9q33	9q33.2		601909	GPR21	G protein-coupled receptor-21	GPR21	2844	ENSG00000011454			Gpr21 (MGI:2441890)			
chr9	123109493	123268575	9q34	9q33.3		611138	"STRBP, SPNR, p74"	Spermatid perinuclear RNA-binding protein	STRBP	55342	ENSG00000165209			Strbp (MGI:104626)			
chr9	123354064	123380334	9q33.3	9q33.3		609720	"CRB2, FSGS9, VMCKD"	"Crumbs, Drosophila, homolog of"	CRB2	286204	ENSG00000148204		"Focal segmental glomerulosclerosis 9, 616220 (3), Autosomal recessive; Ventriculomegaly with cystic kidney disease, 219730 (3), Autosomal recessive"	Crb2 (MGI:2679260)			
chr9	123379653	123930157	9q33.2	9q33.3		613633	"DENND1A, KIAA1608"	DENN/MADD domain-containing protein 1A	DENND1A	57706	ENSG00000119522			Dennd1a (MGI:2442794)			
chr9	124011609	124033162	9q33-q34.1	9q33.3		603759	"LHX2, LH2"	LIM/homeodomain protein LHX2	LHX2	9355	ENSG00000106689			Lhx2 (MGI:96785)			
chr9	124257605	124352441	9q33.3-q34.11	9q33.3		604884	NEK6	Never-in-mitosis gene A-related kinase 6	NEK6	10783	ENSG00000119408			Nek6 (MGI:1891638)			
chr9	124353464	124415472	9q34.11-q34.12	9q33.3		604030	PSMB7	"Proteasome subunit, beta-type, 7"	PSMB7	5695	ENSG00000136930			Psmb7 (MGI:107637)			
chr9	124481235	124507419	9q33	9q33.3		184757	"NR5A1, FTZF1, FTZ1, SF1, AD4BP, POF7, SRXY3, SPGF8, SRXX4"	"Nuclear receptor subfamily 5, group A, member 1"	NR5A1	2516	ENSG00000136931		"Adrenocortical insufficiency, 612964 (3), Autosomal dominant; Premature ovarian failure 7, 612964 (3), Autosomal dominant; Spermatogenic failure 8, 613957 (3), Autosomal dominant; 46, XX sex reversal 4, 617480 (3), Autosomal dominant; 46XY sex reversal 3, 612965 (3), Autosomal dominant"	Nr5a1 (MGI:1346833)			
chr9	124517274	124771309	9q33-q34.1	9q33.3		602778	GCNF	Germ cell nuclear factor	NR6A1	2649	ENSG00000148200			Nr6a1 (MGI:1352459)			
chr9	124692441	124692550	9q33.3	9q33.3		612743	"MIR181A2, MIRN181A2"	Micro RNA 181A2	MIR181A2	406954							
chr9	124693709	124693797	9q33.3	9q33.3		612745	"MIR181B2, MIRN181B2"	Micro RNA 181B2	MIR181B2	406956							
chr9	124777157	124814890	9q33.3	9q33.3		615899	OLFML2A	Olfactomedin-like 2A	OLFML2A	169611	ENSG00000185585			Olfml2a (MGI:2444741)			
chr9	124878293	124941406	9q33.3	9q33.3		602502	GOLGA1	"Golgi autoantigen, golgin subfamily A, 1"	GOLGA1	2800	ENSG00000136935			Golga1 (MGI:1924149)			
chr9	125146572	125189938	9q33.3	9q33.3		612725	PPP6C	"Protein phosphatase 6, catalytic subunit"	PPP6C	5537	ENSG00000119414	highly related sequence on Xq22.3		Ppp6c (MGI:1915107)			
chr9	125234847	125241386	9q34	9q33.3		138120	"HSPA5, GRP78"	"Heat-shock 70kD protein-5 (glucose-regulated protein, 78kD)"	HSPA5	3309	ENSG00000044574			Hspa5 (MGI:95835)			
chr9	125261793	125367206	9q33.3	9q33.3		611714	"GAPVD1, RAP6, GAPEX5, KIAA1521"	GTPase-activating protein and VPS9 domains 1	GAPVD1	26130	ENSG00000165219			Gapvd1 (MGI:1913941)			
chr9	125437393	125707233	9q33.3	9q33.3		610558	"MAPKAP1, SIN1, MIP1, JC310"	Mitogen-activated protein kinase-associated protein 1	MAPKAP1	79109	ENSG00000119487			Mapkap1 (MGI:2444554)			
chr9	125747337	125967376	9q33-q34	9q33.3		176312	PBX3	Pre-B-cell leukemia transcription factor-3	PBX3	5090	ENSG00000167081			Pbx3 (MGI:97496)			
chr9	126614442	126701031	9q34.1	9q33.3		602575	"LMX1B, NPS1"	"LIM homeo box transcription factor 1, beta"	LMX1B	4010	ENSG00000136944		"Nail-patella syndrome, 161200 (3), Autosomal dominant"	Lmx1b (MGI:1100513)			
chr9	126860664	126885877	9q33.3	9q33.3		611692	"ZBTB34, KIAA1993"	Zinc finger- and BTB domain-containing protein 34	ZBTB34	403341	ENSG00000177125			Zbtb34 (MGI:2685195)			
chr9	126914773	127223165	9q33.3	9q33.3		614444	"RALGPS1, RALGEF2, KIAA0351"	Ral guanine nucleotide exchange factor with PH domain and SH3 domain-binding motif 1	RALGPS1	9649	ENSG00000136828			Ralgps1 (MGI:1922008)			
chr9	127087348	127122764	9q33.3	9q33.3		605001	"ANGPTL2, ARP2"	Angiopoietin-like 2	ANGPTL2	23452	ENSG00000136859			Angptl2 (MGI:1347002)			
chr9	127397137	127407897	Chr.9	9q33.3		605245	"SLC2A8, GLUT8"	"Solute carrier family 2, (facilitated glucose transporter) member 8"	SLC2A8	29988	ENSG00000136856			Slc2a8 (MGI:1860103)			
chr9	127424373	127446288	9q34	9q33.3		194552	ZNF79	Zinc finger protein-79 (pT7)	ZNF79	7633	ENSG00000196152						
chr9	127447673	127451431	9q33.3	9q33.3		180475	RPL12	Ribosomal protein L12	RPL12	6136	ENSG00000197958			Rpl12 (MGI:98002)			
chr9	127451485	127503500	9q33.3-q34.11	9q33.3-q34.1		610933	"LRSAM1, TAL, RIFLE, CMT2P"	Leucine-rich repeat- and sterile alpha motif-containing 1	LRSAM1	90678	ENSG00000148356		"Charcot-Marie-Tooth disease, axonal, type 2P, 614436 (3), Autosomal recessive, Autosomal dominant"	Lrsam1 (MGI:2684789)			
chr9	127500000	133100000	9q34.1			612557	CLLS3	"Leukemia, chronic lymphocytic, susceptibility to, 3"		100270642		associated with SNP -6531 upstream of DAPK1 promoter	"{Leukemia, chronic lymphocytic, susceptibility to, 3}, 612557 (2)"				
chr9	127500000	138394717	9q34			614623	KTCN6	Keratoconus 6		100885802		max lod at 159cM	"Keratoconus 6, 614623 (2), Autosomal dominant"				
chr9	127505337	127579006	9q34.13	9q34.11		614045	"FAM129B, MINERVA"	"Family with sequence similarity 129, member B"	FAM129B	64855	ENSG00000136830			Fam129b (MGI:2442910)			
chr9	127612206	127692715	9q34.1	9q34.11		602926	"STXBP1, UNC18, EIEE4"	Syntaxin-binding protein 1	STXBP1	6812	ENSG00000136854		"Epileptic encephalopathy, early infantile, 4, 612164 (3), Autosomal dominant"	Stxbp1 (MGI:107363)			
chr9	127731523	127735348	9q34.11	9q34.11		608052	"TOR2A, TORP1"	Torsin 2A	TOR2A	27433	ENSG00000160404			Tor2a (MGI:1353596)			
chr9	127738316	127778768	9q34.11	9q34.11		604722	"SH2D3C, NSP3"	SH2 domain-containing protein 3C	SH2D3C	10044	ENSG00000095370			Sh2d3c (MGI:1351631)			
chr9	127785537	127790781	9q34.1	9q34.11		603251	"CDK9, CDC2L4"	Cyclin-dependent kinase-9	CDK9	1025	ENSG00000136807			Cdk9 (MGI:1328368)			
chr9	127785917	127786006	9q34.11	9q34.11		613405	"MIR2861, MIRN2861, BMND15"	Micro RNA 2861	MIR2861	100422910			"[Bone mineral density QTL 15], 613418 (3), Autosomal recessive, Autosomal dominant"				
chr9	127802857	127814519	9cen-q34	9q34.11		136510	FPGS	Folylpolyglutamate synthetase	FPGS	2356	ENSG00000136877			Fpgs (MGI:95576)			
chr9	127815011	127854772	9q34.1	9q34.11		131195	"ENG, END, HHT1, ORW"	Endoglin	ENG	2022	ENSG00000106991		"Telangiectasia, hereditary hemorrhagic, type 1, 187300 (3), Autosomal dominant"	Eng (MGI:95392)			
chr9	127866479	127885541	9q34.1	9q34.11		103000	AK1	Adenylate kinase-1	AK1	203	ENSG00000106992	"proximal to Ph1 break, 9q34.1; AK1 to ORM = 17cM"	"Hemolytic anemia due to adenylate kinase deficiency, 612631 (3), Autosomal recessive"	Ak1 (MGI:87977)			
chr9	127885320	127906763	9q34.11	9q34.11		610135	"ST6GALNAC6, SIAT7F"	"ST6 alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6"	ST6GALNAC6	30815	ENSG00000160408			St6galnac6 (MGI:1355316)			
chr9	127907885	127917051	9q31	9q34.11		606378	"SIAT7D, SIAT3C"	Sialyltransferase 7D	ST6GALNAC4	27090	ENSG00000136840			St6galnac4 (MGI:1341894)			
chr9	127920885	127931957	9q34.11	9q34.11		612865	"PIP5KL1, PIPKH"	Phosphatidylinositol-4-phosphate-5-kinase-like 1	PIP5KL1	138429	ENSG00000167103			Pip5kl1 (MGI:2448520)			
chr9	127935094	127938483	9q34.11	9q34.11		603564	"DPM2, CDG1U"	"Dolichyl-phosphate mannosyltransferase 2, regulatory subunit"	DPM2	8818	ENSG00000136908		"Congenital disorder of glycosylation, type Iu, 615042 (3), Autosomal recessive"	Dpm2 (MGI:1330238)			
chr9	127940581	127980532	9q34.13	9q34.11		610891	"FAM102A, EEIG1"	"Family with sequence similarity 102, member A"	FAM102A	399665	ENSG00000167106			Fam102a (MGI:2138935)			
chr9	128061232	128067866	9q34.11	9q34.11		610673	"C9orf90, NAIF1"	Nuclear apoptosis-inducing factor 1	NAIF1	203245	ENSG00000171169			Naif1 (MGI:1918504)			
chr9	128120692	128128461	9q34.13	9q34.11		608152	"PTGES2, PGES2, GBF1"	Prostaglandin E synthase 2	PTGES2	80142	ENSG00000148334			Ptges2 (MGI:1917592)			
chr9	128149429	128153454	9q34	9q34.11		600181	"LCN2, NGAL"	Lipocalin 2 (oncogene 24p3)	LCN2	3934	ENSG00000148346			Lcn2 (MGI:96757)			
chr9	128166064	128204382	9q34	9q34.11		611420	"CIZ1, ZNF356, LSFR1, NP94"	CDKN1A-interacting zinc finger protein 1	CIZ1	25792	ENSG00000148337			Ciz1 (MGI:1920234)			
chr9	128203354	128255247	9q34	9q34.11		602377	"DNM1, EIEE31"	Dynamin-1	DNM1	1759	ENSG00000106976		"Epileptic encephalopathy, early infantile, 31, 616346 (3), Autosomal dominant"	Dnm1 (MGI:107384)			
chr9	128244720	128244829	9q34.11	9q34.11		614791	MIR199B	Micro RNA 199B	MIR199B	406978							
chr9	128255828	128276006	9q34.11	9q34.11		602580	"GOLGA2, GM130"	"Golgi autoantigen, golgin subfamily A, 2"	GOLGA2	2801	ENSG00000167110			Golga2 (MGI:2139395)			
chr9	128275363	128288989	9q34.11	9q34.11		616528	"SWI5, SAE3, C9orf119"	SWi5 homologous recombination repair protein	SWI5	375757	ENSG00000175854			Swi5 (MGI:1920181)			
chr9	128309099	128322779	9q34.11	9q34.11		610727	TRUB2	"TRUB pseudouridine synthase, E. coli, homolog of, 2"	TRUB2	26995	ENSG00000167112			Trub2 (MGI:2442186)			
chr9	128322485	128334071	9q34.13	9q34.11		612898	"COQ4, COQ10D7"	"Coenzyme Q4, S. cerevisiae, homolog of"	COQ4	51117	ENSG00000167113		"Coenzyme Q10 deficiency, primary, 7, 616276 (3), Autosomal recessive"	Coq4 (MGI:1098826)			
chr9	128340515	128361469	9q34	9q34.11		604194	"SLC27A4, FATP4, IPS"	"Solute carrier family 27 (fatty acid transporter), member 4"	SLC27A4	10999	ENSG00000167114		"Ichthyosis prematurity syndrome, 608649 (3)"	Slc27a4 (MGI:1347347)			
chr9	128371318	128392015	9q34.11	9q34.11		612693	URM1	"Ubiquitin-related modifier 1, S. cerevisiae, homolog of"	URM1	81605	ENSG00000167118			Urm1 (MGI:1915455)			
chr9	128405993	128437350	9q34.11	9q34.11		616626	CERCAM	Cerebral endothelial cell adhesion molecule	CERCAM	51148	ENSG00000167123			Cercam (MGI:2139134)			
chr9	128455154	128501291	9q34	9q34.11		602015	"ODF2, ODF84"	Outer dense fiber of sperm tails 2	ODF2	4957	ENSG00000136811			Odf2 (MGI:1098824)			
chr9	128504691	128542300	9q34	9q34.11		603371	"GLE1, GLE1L, LCCS, LCCS1"	"Gle1, RNA export mediator, S. cerevisiae, homolog of"	GLE1	2733	ENSG00000119392		"Arthrogryposis, lethal, with anterior horn cell disease, 611890 (3); Lethal congenital contracture syndrome 1, 253310 (3), Autosomal recessive"	Gle1 (MGI:1921662)			
chr9	128552557	128633664	9q33-q34	9q34.11		182810	"SPTAN1, NEAS, EIEE5"	"Spectrin, alpha, nonerythrocytic-1 (alpha-fodrin)"	SPTAN1	6709	ENSG00000197694		"Epileptic encephalopathy, early infantile, 5, 613477 (3), Autosomal dominant"	Sptan1 (MGI:98386)			
chr9	128633652	128656849	9q34.11	9q34.11		613363	"WDR34, SRTD11"	WD repeat-containing protein 34	WDR34	89891	ENSG00000119333		"Short-rib thoracic dysplasia 11 with or without polydactyly, 615633 (3), Autosomal recessive"	Wdr34 (MGI:1919070)			
chr9	128683431	128696395	9q34	9q34.11		600960	SET	SET gene	SET	6418	ENSG00000119335	fused with CAIN in acute undifferentiated leukemia		Set (MGI:1860267)			
chr9	128702496	128720919	9q34.11	9q34.11		610714	PKN3	Protein kinase N3	PKN3	29941	ENSG00000160447			Pkn3 (MGI:2388285)			
chr9	128729785	128772506	9q34.11	9q34.11		617764	"ZER1, ZYG11BL, C9orf60"	Zyg11-related cell cycle regulator	ZER1	10444	ENSG00000160445			Zer1 (MGI:2442511)			
chr9	128787206	128810431	9q34.11	9q34.11		616218	TBC1D13	"TBC1 domain family, member 13"	TBC1D13	54662	ENSG00000107021			Tbc1d13 (MGI:2385326)			
chr9	128818401	128822675	9q34.1	9q34.11		600440	ENDOG	Endonuclease G	ENDOG	2021	ENSG00000167136			Endog (MGI:1261433)			
chr9	128819650	128833308	9q34.11	9q34.11		617614	"SPOUT1, CENP32, C9orf114"	SPOUT domain-containing methyltransferase 1	SPOUT1	51490	ENSG00000198917			Spout1 (MGI:106544)			
chr9	128833112	128882557	9q34.11	9q34.11		600547	CCBL1	Cysteine conjugate beta-lyase 1	KYAT1	883	ENSG00000171097			Kyat1 (MGI:1917516)			
chr9	128882111	128918041	9q34.13	9q34.11		608360	"LRRC8A, KIAA1437, AGM5"	Leucine-rich repeat-containing 8A	LRRC8A	56262	ENSG00000136802	mutation identified in 1 AGM5 patient	"?Agammaglobulinemia 5, 613506 (3), Autosomal dominant"	Lrrc8a (MGI:2652847)			
chr9	128945529	128947732	9q34.11	9q34.11		610746	"DOLK, TMEM15, DK1, SEC59, KIAA1094, CDG1M"	Dolichol kinase	DOLK	22845	ENSG00000175283		"Congenital disorder of glycosylation, type Im, 610768 (3), Autosomal recessive"	Dolk (MGI:2677836)			
chr9	128947692	129007095	9q34.11	9q34.11		615587	"NUP188, KIAA1069"	"Nucleoporin, 188kD"	NUP188	23511	ENSG00000095319			Nup188 (MGI:2446190)			
chr9	129080987	129090437	9q34.1	9q34.11		614516	"DOLPP1, LSFR2"	Dolichyl pyrophosphate phosphatase 1	DOLPP1	57171	ENSG00000167130			Dolpp1 (MGI:1914093)			
chr9	129094793	129110797	9q34.1	9q34.11		600184	"CRAT, CAT1, NBIA8"	Carnitine acetyltransferase	CRAT	1384	ENSG00000095321	mutation identified in 1 NBIA8 patient	"?Neurodegeneration with brain iron accumulation 8, 617917 (3), Autosomal recessive"	Crat (MGI:109501)			
chr9	129110948	129148945	9q34	9q34.11		600756	"PPP2R4, PTPA"	"Protein phosphatase-2A, regulatory subunit B' (PR 53)"	PTPA	5524	ENSG00000119383	proximal to ABL		Ptpa (MGI:1346006)			
chr9	129608883	129636741	9q34.11	9q34.11		613560	"NTMT1, METTL11A, NRMT, C9orf32"	N-terminal X-Pro-Lys N-methyltransferase 1	NTMT1	28989	ENSG00000148335			Ntmt1 (MGI:1913867)			
chr9	129634603	129642168	9q34.11	9q34.11		615051	ASB6	Ankyrin repeat- and SOCS box-containing protein 6	ASB6	140459	ENSG00000148331			Asb6 (MGI:1919573)			
chr9	129665640	129722673	9q34.1	9q34.11		604675	"PRRX2, PRX2"	Paired-related homeo box gene 2	PRRX2	51450	ENSG00000167157			Prrx2 (MGI:98218)			
chr9	129738335	129777578	9q34.3	9q34.11		605172	"PTGES, PGES, PIG12, MGST1L1"	Prostaglandin E synthase	PTGES	9536	ENSG00000148344			Ptges (MGI:1927593)			
chr9	129803142	129811423	9q34	9q34.11		608050	"TOR1B, DQ1"	Torsin 1B	TOR1B	27348	ENSG00000136816	centromeric to TOR1A; pseudogene on chr.2		Tor1b (MGI:1353605)			
chr9	129812941	129824161	9q34	9q34.11		605204	"DYT1, TOR1A"	Torsin A	TOR1A	1861	ENSG00000136827		"{Dystonia-1, modifier of} (3); Dystonia-1, torsion, 128100 (3), Autosomal dominant"	Tor1a (MGI:1353568)			
chr9	129835416	129881837	9q34.11	9q34.11		615143	"USP20, VDU2"	Ubiquitin-specific protease 20	USP20	10868	ENSG00000136878			Usp20 (MGI:1921520)			
chr9	129887186	130053845	9q34	9q34.11		606191	"FNBP1, FBP17"	Formin-binding protein 17	FNBP1	23048	ENSG00000187239	fused with MLL in chronic myeloid leukemia		Fnbp1 (MGI:109606)			
chr9	130172577	130237303	9q34	9q34.11		603315	"FREQ, NCS1"	"Frequenin, Drosophila, homolog of"	NCS1	23413	ENSG00000107130			Ncs1 (MGI:109166)			
chr9	130444706	130501273	9q34.1	9q34.11		603470	"ASS1, ASS"	Argininosuccinate synthetase 1	ASS1	445	ENSG00000130707	"14 pseudogenes on 11 chromosomes, including X and Y and ASSP2 on 6p23-q12"	"Citrullinemia, 215700 (3), Autosomal recessive"	Ass1 (MGI:88090)			
chr9	130579572	130638351	9q34.11-q34.12	9q34.11-q34.12		603536	"FUBP3, FBP3"	FAR upstream element-binding protein 3	FUBP3	8939	ENSG00000107164			Fubp3 (MGI:2443699)			
chr9	130664593	130682996	9q34.1	9q34.12		616458	"PRDM12, HSAN8"	PR domain-containing protein 12	PRDM12	59335	ENSG00000130711		"Neuropathy, hereditary sensory and autonomic, type VIII, 616488 (3), Autosomal recessive"	Prdm12 (MGI:2685844)			
chr9	130693759	130704893	9q34.12	9q34.12		602238	"EXOSC2, RRP4, SHRF"	Exosome component 2	EXOSC2	23404	ENSG00000130713		"Short stature, hearing loss, retinitis pigmentosa, and distinctive facies, 617763 (3), Autosomal recessive"	Exosc2 (MGI:2385133)			
chr9	130713880	130887674	9q34.1	9q34.12		189980	"ABL1, CHDSKM"	Abelson murine leukemia viral (v-abl) oncogene homolog 1	ABL1	25	ENSG00000097007	fusion hybrid gene with BCR1 in CML	"Congenital heart defects and skeletal malformations syndrome, 617602 (3), Autosomal dominant; Leukemia, Philadelphia chromosome-positive, resistant to imatinib (3)"	Abl1 (MGI:87859)			
chr9	130893427	130896811	9q34.12	9q34.12		609795	"QRFP, P518, 26RFA"	Pyroglutamylated FR-amide peptide precursor protein	QRFP	347148	ENSG00000188710			Qrfp (MGI:3630329)			
chr9	130902437	130939067	9q34.1	9q34.12		613357	FIBCD1	Fibrinogene C domain-containing protein 1	FIBCD1	84929	ENSG00000130720			Fibcd1 (MGI:2138953)			
chr9	131009116	131093058	9q33-q34	9q34.12		604349	"LAMC3, OCCM"	"Laminin, gamma-3"	LAMC3	10319	ENSG00000050555		"Cortical malformations, occipital, 614115 (3), Autosomal recessive"	Lamc3 (MGI:1344394)			
chr9	131100000	133100000	9q34.13			171720	ALPQTL1	"Alkaline phosphatase, plasma level of, QTL 1"		100196909		linkage with rs657152	"{Alkaline phosphatase, plasma level of, QTL1}, 171720 (2), ?Autosomal dominant"				
chr9	131125560	131234669	9q34.1	9q34.13		114350	"NUP214, D9S46E, CAN, CAIN"	"Nucleoporin, 214kD"	NUP214	8021	ENSG00000126883	fused with DEK in AML; fused with ABL1 in T-ALL	"Leukemia, T-cell acute lymphoblastic, somatic, 613065 (3); Leukemia, acute myeloid, somatic, 601626 (3)"	Nup214 (MGI:1095411)			
chr9	131502901	131523805	9q34.1	9q34.13		607423	"POMT1, MDDGA1, MDDGB1, MDDGC1"	Protein O-mannosyltransferase 1	POMT1	10585	ENSG00000130714		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1, 613155 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1, 609308 (3), Autosomal recessive"	Pomt1 (MGI:2138994)			
chr9	131523795	131531274	9q34.2	9q34.13		609328	UCK1	Uridine/cytidine kinase 1	UCK1	83549	ENSG00000130717			Uck1 (MGI:98904)			
chr9	131576769	131740067	9q34.3	9q34.13		600303	"RAPGEF1, GRF2, C3G"	RAP guanine nucleotide exchange factor 1	RAPGEF1	2889	ENSG00000107263			Rapgef1 (MGI:104580)			
chr9	131860109	132079886	9q34	9q34.13		605044	"MED27, CRSP8, CRAP34"	Mediator complex subunit 27	MED27	9442	ENSG00000160563			Med27 (MGI:1916225)			
chr9	132261355	132356725	9q34	9q34.13		608465	"SETX, SCAR1, AOA2, ALS4"	Senataxin	SETX	23064	ENSG00000107290		"Amyotrophic lateral sclerosis 4, juvenile, 602433 (3), Autosomal dominant; Spinocerebellar ataxia, autosomal recessive 1, 606002 (3), Autosomal recessive"	Setx (MGI:2443480)			
chr9	132375547	132406850	9q34.13	9q34.13		600777	TTF1	"Transcription termination factor, RNA polymerase I"	TTF1	7270	ENSG00000125482						
chr9	132582605	132590252	9q34	9q34.13		605211	BARHL1	BARH-like 1	BARHL1	56751	ENSG00000125492			Barhl1 (MGI:1859288)			
chr9	132592996	132670400	9q34.13	9q34.13		616533	"DDX31, PPP1R25"	DEAD box polypeptide 31	DDX31	64794	ENSG00000125485			Ddx31 (MGI:2682639)			
chr9	132725573	132878810	9q34.13	9q34.13		615365	AK8	Adenylate kinase 8	AK8	158067	ENSG00000165695			Ak8 (MGI:1916120)			
chr9	132891347	132945268	9q34	9q34.13		605284	"TSC1, LAM"	Hamartin (tuberous sclerosis 1 gene)	TSC1	7248	ENSG00000165699	"linked to ABO, ABL"	"Focal cortical dysplasia, type II, somatic, 607341 (3); Lymphangioleiomyomatosis, 606690 (3); Tuberous sclerosis-1, 191100 (3), Autosomal dominant"	Tsc1 (MGI:1929183)			
chr9	132945544	132991696	9q34.13	9q34.13		604383	"GFI1B, BDPLT17"	Growth factor-independent 1B	GFI1B	8328	ENSG00000165702		"Bleeding disorder, platelet-type, 17, 187900 (3), Autosomal recessive, Autosomal dominant"	Gfi1b (MGI:1276578)			
chr9	133030674	133058502	9q34.2	9q34.13		604890	"GTF3C5, TFIIIC63"	"General transcription factor 3C, polypeptide 5"	GTF3C5	9328	ENSG00000148308			Gtf3c5 (MGI:1917489)			
chr9	133061977	133071862	9q34.3	9q34.13		114840	"CEL, BSSL, CELL, MODY8"	Carboxyl-ester lipase (bile-salt stimulated lipase)	CEL	1056	ENSG00000170835		"Maturity-onset diabetes of the young, type VIII, 609812 (3), Autosomal dominant"	Cel (MGI:88374)			
chr9	133097719	133149219	9q34	9q34.1-q34.2		601619	RALGDS	ral guanine nucleotide dissociation stimulator	RALGDS	5900	ENSG00000160271			Ralgds (MGI:107485)			
chr9	133152947	133163944	9q34	9q34.2		606074	"GBGT1, FS"	"Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (Forssman synthetase)"	GBGT1	26301	ENSG00000148288			Gbgt1 (MGI:2449143)			
chr9	133205278	133223254	9q34	9q34.2		604606	OBP2B	Odorant-binding protein 2B	OBP2B	29989	ENSG00000171102			Obp2a (MGI:2387617)			
chr9	133255175	133275213	9q34	9q34.2		110300	ABO	ABO glycosyltransferase	ABO	28	ENSG00000175164	linked to AK1	"[Blood group, ABO system], 616093 (3)"	Abo (MGI:2135738)			
chr9	133330706	133336209	9q34	9q34.2		185642	SURF6	Surfeit-6	SURF6	6838	ENSG00000148296			Surf6 (MGI:98447)			
chr9	133340900	133348155	9q34	9q34.2		185641	SURF5	Surfeit-5	MED22	6837	ENSG00000148297			Med22 (MGI:98446)			
chr9	133348213	133351424	9q34	9q34.2		185640	"RPL7A, SURF3"	Ribosomal protein L7a (surfeit-3)	RPL7A	6130	ENSG00000148303	in cluster with SURF1		Rpl7a (MGI:1353472)			
chr9	133351804	133356484	9q34	9q34.2		185620	"SURF1, CMT4K"	Surfeit-1	SURF1	6834	ENSG00000148290	"distal to ABL, CAN"	"Charcot-Marie-Tooth disease, type 4K, 616684 (3), Autosomal recessive; Leigh syndrome, due to COX IV deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Surf1 (MGI:98443)			
chr9	133356544	133361164	9q34	9q34.2		185630	SURF2	Surfeit-2	SURF2	6835	ENSG00000148291			Surf2 (MGI:98444)			
chr9	133361448	133377948	9q34	9q34.2		185660	SURF4	Surfeit-4	SURF4	6836	ENSG00000148248			Surf4 (MGI:98445)			
chr9	133406057	133418171	9q34	9q34.2		602930	"REXO4, XPMC2H"	"RNA exonuclease 4, S. cerevisiae, homolog of"	REXO4	57109	ENSG00000148300			Rexo4 (MGI:2684957)			
chr9	133414338	133459402	9q34	9q34.2		604134	"ADAMTS13, VWFCP, TTP"	"A disintegrin-like and metalloprotease with thrombospondin type 1 motif, 13"	ADAMTS13	11093	ENSG00000160323		"Thrombotic thrombocytopenic purpura, familial, 274150 (3), Autosomal recessive"	Adamts13 (MGI:2685556)			
chr9	133459964	133470786	9q34.2	9q34.2		613104	"C9orf7, FLOWER"	"Flower, Drosophila, homolog of"	CACFD1	11094	ENSG00000160325			Cacfd1 (MGI:1924317)			
chr9	133471093	133479153	9q34	9q34.2		606813	SLC2A6	"Solute carrier family 2, member 6"	SLC2A6	11182	ENSG00000160326			Slc2a6 (MGI:2443286)			
chr9	133514585	133524945	9q34.2	9q34.2		615345	"MYMK, TMEM8C"	Myomaker	MYMK	389827	ENSG00000187616		"Carey-Fineman-Ziter syndrome, 254940 (3), Autosomal recessive"	Mymk (MGI:1913389)			
chr9	133532163	133575518	9q34.2	9q34.2		612277	"ADAMTSL2, KIAA0605, GPHYSD1"	ADAMTS-like protein 2	ADAMTSL2	9719	ENSG00000197859		"Geleophysic dysplasia 1, 231050 (3), Autosomal recessive"	Adamtsl2 (MGI:1925044)			
chr9	133636362	133659343	9q34	9q34.2		609312	DBH	Dopamine-beta-hydroxylase	DBH	1621	ENSG00000123454	tightly linked to ABO	"Dopamine beta-hydroxylase deficiency, 223360 (3), Autosomal recessive; [Dopamine-beta-hydroxylase activity levels, plasma] (3)"	Dbh (MGI:94864)			
chr9	133663073	133739957	9q34.2	9q34.2		604455	"SARDH, SARD, SAR"	Sarcosine dehydrogenase	SARDH	1757	ENSG00000123453		"[Sarcosinemia], 268900 (3), Autosomal recessive"	Sardh (MGI:2183102)			
chr9	133761893	133992373	9q34	9q34.2		600428	VAV2	Oncogene VAV2	VAV2	7410	ENSG00000160293			Vav2 (MGI:102718)			
chr9	134030304	134068532	9q34	9q34.2		601541	"RING3L, ORFX"	RING3-like gene (open reading frame X)	BRD3	8019	ENSG00000169925			Brd3 (MGI:1914632)			
chr9	134164439	134164563	9q34.2	9q34.2		601429	"RNU6ATAC, U6ATAC"	"RNA, U6ATAC small nuclear"	RNU6ATAC	100151684							
chr9	134326462	134440585	9q34.3	9q34.2		180245	RXRA	"Retinoid X receptor, alpha"	RXRA	6256	ENSG00000186350	distal to DBH		Rxra (MGI:98214)			
chr9	134641788	134844842	9q34.2-q34.3	9q34.3		120215	"COL5A1, EDSCL1"	"Collagen V, alpha-1 polypeptide"	COL5A1	1289	ENSG00000130635		"Ehlers-Danlos syndrome, classic type, 1, 130000 (3), Autosomal dominant"	Col5a1 (MGI:88457)			
chr9	134864061	134890505	9q34	9q34.3		601624	FCN2	Ficolin (collagen/fibrinogen domain-containing lectin) 2	FCN2	2220	ENSG00000160339						
chr9	134903235	134918002	9q34	9q34.3		601252	FCN1	Ficolin (collagen/fibrinogen domain-containing) 1	FCN1	2219	ENSG00000085265			Fcnb (MGI:1341158)			
chr9	135075242	135121183	Chr.9	9q34.3		605366	"OLFM1, AMY"	Olfactomedin 1	OLFM1	10439	ENSG00000130558			Olfm1 (MGI:1860437)			
chr9	135477649	135488893	9q34.3	9q34.3		614056	"PPP1R26, KIAA0649"	"Protein phosphatase 1, regulatory subunit 26"	PPP1R26	9858	ENSG00000196422			Ppp1r26 (MGI:2685193)			
chr9	135495179	135499914	9q34.3	9q34.3		614502	"C9orf116, PIERCE1"	p53-induced expression in RB-null cells 1	C9orf116	138162	ENSG00000160345			1700007K13Rik (MGI:1916577)			
chr9	135499988	135504672	9q34	9q34.3		611971	MRPS2	Mitochondrial ribosomal protein S2	MRPS2	51116	ENSG00000122140			Mrps2 (MGI:2153089)			
chr9	135521295	135526539	9q34	9q34.3		151675	LCN1	"Lipocalin 1 (protein migrating faster than albumin, tear prealbumin)"	LCN1	3933	ENSG00000160349						
chr9	135544811	135549968	9q34	9q34.3		164320	OBP2A	Odorant-binding protein 2A	OBP2A	29991	ENSG00000122136			Obp2b (MGI:3651927)			
chr9	135561626	135566775	9q34	9q34.3		173310	"PAEP, PP14"	Progestagen-associated endometrial protein (placental protein 14)	PAEP	5047	ENSG00000122133						
chr9	135623655	135641223	9q34.3	9q34.3		613699	"GLT6D1, GT6M7, GLTDC1"	Glycosyltransferase 6 domain-containing 1	GLT6D1	360203	ENSG00000204007			Glt6d1 (MGI:1918353)			
chr9	135663321	135670730	9q34	9q34.3		612903	LCN9	Lipocalin 9	LCN9	392399	ENSG00000148386			Lcn9 (MGI:1924954)			
chr9	135691861	135702111	9q34.3	9q34.3		610224	"SOHLH1, NOHLH, TEB2, ODG5"	Spermatogenesis- and oogenesis-specific basic helix-look-helix protein 1	SOHLH1	402381	ENSG00000165643		"Ovarian dysgenesis 5, 617690 (3), Autosomal recessive"	Sohlh1 (MGI:2684956)			
chr9	135702184	135793146	9q34.3	9q34.3		608167	"KCNT1, KIAA1422, EIEE14, ENFL5"	"Potassium channel, subfamily T, member 1"	KCNT1	57582	ENSG00000107147		"Epilepsy, nocturnal frontal lobe, 5, 615005 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 14, 614959 (3), Autosomal dominant"	Kcnt1 (MGI:1924627)			
chr9	135808486	135907550	9q34.3	9q34.3		613774	CAMSAP1	Calmodulin-regulated spectrin-associated protein 1	CAMSAP1	157922	ENSG00000130559			Camsap1 (MGI:3036242)			
chr9	135932968	135961379	9q34.3	9q34.3		608129	"UBAC1, GBDR1"	Ubiquitin-associated domain-containing protein 1	UBAC1	10422	ENSG00000130560			Ubac1 (MGI:1920995)			
chr9	136006536	136095284	9q34.3	9q34.3		615786	"NACC2, RBB"	"NACC family, member 2, BEN and BTB/POZ domains-containing"	NACC2	138151	ENSG00000148411			Nacc2 (MGI:1915241)			
chr9	136196249	136205128	9q34.3	9q34.3		600577	"LHX3, CPHD3"	LIM/homeodomain protein LHX3	LHX3	8022	ENSG00000107187	"in mouse, close to Notch1; centromeric to ABL"	"Pituitary hormone deficiency, combined, 3, 221750 (3), Autosomal recessive"	Lhx3 (MGI:102673)			
chr9	136206332	136245840	9q34.3	9q34.3		612860	"QSOX2, SOXN"	Quiescin Q6 sulfhydryl oxidase 2	QSOX2	169714	ENSG00000165661			Qsox2 (MGI:2387194)			
chr9	136363955	136373680	9q34.3	9q34.3		607212	"CARD9, CANDF2"	Caspase recruitment domain-containing protein 9	CARD9	64170	ENSG00000187796		"Candidiasis, familial, 2, autosomal recessive, 212050 (3), Autosomal recessive"	Card9 (MGI:2685628)			
chr9	136375568	136400219	9q34.3	9q34.3		602777	"SNAPC4, SNAP190"	"Small nuclear RNA-activating protein complex, polypeptide 4"	SNAPC4	6621	ENSG00000165684			Snapc4 (MGI:2443935)			
chr9	136410572	136423760	9q34.3	9q34.3		613036	"PMPCA, KIAA0123, SCAR2"	"Peptidase, mitochondrial processing, alpha"	PMPCA	23203	ENSG00000165688		"Spinocerebellar ataxia, autosomal recessive 2, 213200 (3), Autosomal recessive"	Pmpca (MGI:1918568)			
chr9	136428614	136439860	9q34.3	9q34.3		613037	"INPP5E, MORMS, JBTS1, CORS1"	"Inositol polyphosphate-5-phosphatase, 72kD"	INPP5E	56623	ENSG00000148384		"Joubert syndrome 1, 213300 (3), Autosomal recessive; Mental retardation, truncal obesity, retinal dystrophy, and micropenis, 610156 (3), Autosomal recessive"	Inpp5e (MGI:1927753)			
chr9	136440095	136484551	9q34.3	9q34.3		612854	"SEC16A, SEC16L, KIAA0310, p250"	"Sec16, S. Cerevisiae, homolog of, A"	SEC16A	9919	ENSG00000148396			Sec16a (MGI:2139207)			
chr9	136494432	136545785	9q34.3	9q34.3		190198	"NOTCH1, TAN1, AOS5, AOVD1"	"Notch, Drosophila, homolog of, 1, translocation-associated"	NOTCH1	4851	ENSG00000148400		"Adams-Oliver syndrome 5, 616028 (3), Autosomal dominant; Aortic valve disease 1, 109730 (3), Autosomal dominant"	Notch1 (MGI:97363)			
chr9	136654752	136672677	9q34.3	9q34.3		608582	EGFL7	Epidermal growth factor-like 7	EGFL7	51162	ENSG00000172889			Egfl7 (MGI:2449923)			
chr9	136670601	136670685	9q34.3	9q34.3		611767	"MIR126, MIRN126"	Micro RNA 126	MIR126	406913							
chr9	136673142	136687458	9q34.3	9q34.3		603100	"AGPAT2, LPAAB, BSCL, BSCL1"	1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase-beta)	AGPAT2	10555	ENSG00000169692		"Lipodystrophy, congenital generalized, type 1, 608594 (3), Autosomal recessive"	Agpat2 (MGI:1914762)			
chr9	136712571	136724717	9q34.3	9q34.3		614543	FAM69B	"Family with sequence similarity 69, member B"	FAM69B	138311	ENSG00000165716			Fam69b (MGI:1927576)			
chr9	136738166	136742958	9q34	9q34.3		612904	LCN10	Lipocalin 10	LCN10	414332	ENSG00000187922			Lcn10 (MGI:1925000)			
chr9	136744016	136748527	9q34	9q34.3		609379	LCN6	Lipocalin 6	LCN6	158062	ENSG00000267206			Lcn6 (MGI:3045364)			
chr9	136754387	136758550	9q34	9q34.3		612902	LCN8	Lipocalin 8	LCN8	138307	ENSG00000204001			Lcn8 (MGI:2135945)			
chr9	136796337	136807740	9q34.3	9q34.3		615955	"CCDC183, KIAA1984"	Coiled-coil domain-containing protein 183	CCDC183	84960	ENSG00000213213			Ccdc183 (MGI:1924308)			
chr9	136807921	136841186	9q34.3	9q34.3		610615	"RABL6, PARF, C9orf86"	RAB-like protein 6	RABL6	55684	ENSG00000196642			Rabl6 (MGI:2442633)			
chr9	136848815	136851042	9q34.3	9q34.3		610167	PHPT1	Phosphohistidine phosphatase 1	PHPT1	29085	ENSG00000054148			Phpt1 (MGI:1922704)			
chr9	136852366	136860798	9q34.3	9q34.3		617208	MAMDC4	MAM domain-containing protein 4	MAMDC4	158056	ENSG00000177943			Mamdc4 (MGI:2685841)			
chr9	136881932	136926614	9q34.3	9q34.3		601895	"TRAF2, TRAP"	TNF receptor-associated factor 2	TRAF2	7186	ENSG00000127191			Traf2 (MGI:101835)			
chr9	136940432	136944773	9q34.3	9q34.3		609072	"FBXW5, FBW5"	F-box and WD40 domain protein 5	FBXW5	54461	ENSG00000159069			Fbxw5 (MGI:1354731)			
chr9	136944869	136946980	9q34.3	9q34.3		120930	C8G	"Complement component-8, gamma polypeptide"	C8G	733	ENSG00000176919			C8g (MGI:88237)			
chr9	136949179	136955504	9q34	9q34.3		612905	LCN12	Lipocalin 12	LCN12	286256	ENSG00000184925			Lcn12 (MGI:1924951)			
chr9	136977503	136981741	9q34.2-q34.3	9q34.3		176803	PTGDS	"Prostaglandin D2 synthase (21kD, brain)"	PTGDS	5730	ENSG00000107317	distal to ABL		Ptgds (MGI:99261)			
chr9	136992417	136993987	9q34.3	9q34.3		616315	"PAXX, C9orf142"	Paralog of XRCC4 and XLF	PAXX	286257	ENSG00000148362			Paxx (MGI:2442831)			
chr9	136994607	136997928	Chr.9	9q34.3		606533	CLIC3	Chloride intracellular channel 3	CLIC3	9022	ENSG00000169583			Clic3 (MGI:1916704)			
chr9	137007233	137028921	9q34	9q34.3		600047	"ABCA2, ABC2"	ATP-binding cassette 2	ABCA2	20	ENSG00000107331			Abca2 (MGI:99606)			
chr9	137030173	137032839	Chr.9	9q34.3		602030	FUT7	"Fucosyltransferase 7 (alpha (1,3) fucosyltransferase)"	FUT7	2529	ENSG00000180549			Fut7 (MGI:107692)			
chr9	137039456	137046223	Chr.9	9q34.3		605798	"NPDC1, CAB1"	"Neural proliferation, differentiation, and control protein 1"	NPDC1	56654	ENSG00000107281			Npdc1 (MGI:1099802)			
chr9	137048097	137054050	9q34	9q34.3		602012	"ENTPD2, CD39L1"	Ectonucleoside triphosphate diphosphohydrolase 2	ENTPD2	954	ENSG00000054179	same cosmid as ABC2		Entpd2 (MGI:1096863)			
chr9	137062126	137070575	9q34.3	9q34.3		612057	"C9orf140, P42.3"	Chromosome 9 open reading frame 140	SAPCD2	89958	ENSG00000186193			Sapcd2 (MGI:1919330)			
chr9	137086926	137109186	9q34.3	9q34.3		604346	"MAN1B1, MRT15"	"Mannosidase, alpha, class 1B member 1"	MAN1B1	11253	ENSG00000177239		"Mental retardation, autosomal recessive 15, 614202 (3), Autosomal recessive"	Man1b1 (MGI:2684954)			
chr9	137110539	137117979	9q34.3	9q34.3		610537	"DPP7, QPP"	Dipeptidyl peptidase VII	DPP7	29952	ENSG00000176978			Dpp7 (MGI:1933213)			
chr9	137139091	137168761	9q34.3	9q34.3		138249	"GRIN1, NMDAR1, NDHMSR, NDHMSD"	"Glutamate receptor, ionotropic, N-methyl D-aspartate 1"	GRIN1	2902	ENSG00000176884		"Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant, 614254 (3), Autosomal dominant; Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive, 617820 (3), Autosomal recessive"	Grin1 (MGI:95819)			
chr9	137168757	137170038	9q34.3	9q34.3		613505	"LRRC26, CAPC"	Leucine-rich repeat-containing protein 26	LRRC26	389816	ENSG00000184709			Lrrc26 (MGI:2385129)			
chr9	137188601	137190369	9q34.3	9q34.3		610882	"SSNA1, NA14"	Sjogren syndrome nuclear autoantigen 1	SSNA1	8636	ENSG00000176101			Ssna1 (MGI:1915725)			
chr9	137174783	137188604	Chr.9	9q34.3		606946	"ANAPC2, APC2, KIAA1406"	"Anaphase-promoting complex, subunit 2"	ANAPC2	29882	ENSG00000176248			Anapc2 (MGI:2139135)			
chr9	137191616	137200710	9q34.3	9q34.3		613354	"TPRN, C9orf75, DFNB79"	Taperin	TPRN	286262	ENSG00000176058		"Deafness, autosomal recessive 79, 613307 (3), Autosomal recessive"	Tprn (MGI:2139535)			
chr9	137204081	137205637	9q34.3	9q34.3		616499	TMEM203	Transmembrane protein 203	TMEM203	94107	ENSG00000187713			Tmem203 (MGI:2443597)			
chr9	137205666	137219360	9q34.3	9q34.3		606073	NR1	NADPH-dependent FMN- and FAD-containing oxidoreductase	NDOR1	27158	ENSG00000188566			Ndor1 (MGI:1926047)			
chr9	137230756	137236553	9q34	9q34.3		609826	"SLC34A3, NPTIIC, HHRH"	"Solute carrier family 34 (sodium/phosphate cotransporter), member 3"	SLC34A3	142680	ENSG00000198569		"Hypophosphatemic rickets with hypercalciuria, 241530 (3), Autosomal recessive"	Slc34a3 (MGI:2159410)			
chr9	137241258	137243706	9q34.3	9q34.3		602660	"TUBB4B, TUBB2C, LCAEOD"	"Tubulin, beta-4B"	TUBB4B	10383	ENSG00000188229		"Leber congenital amaurosis with early-onset deafness, 617879 (3), Autosomal dominant"	Tubb4b (MGI:1915472)			
chr9	137255299	137273547	9q34	9q34.3		611180	"COBRA1, NELFB, KIAA1182"	Cofactor of BRCA1	NELFB	25920	ENSG00000188986			Nelfb (MGI:1931035)			
chr9	137423371	137434405	9q34.3	9q34.3		611255	NOXA1	NADPH oxidase activator 1	NOXA1	10811	ENSG00000188747			Noxa1 (MGI:2449980)			
chr9	137434363	137441709	9q34	9q34.3		616748	ENTPD8	Ectonucleoside triphosphate diphosphohydrolase 8	ENTPD8	377841	ENSG00000188833			Entpd8 (MGI:1919340)			
chr9	137447569	137459333	9q34.3	9q34.3		608137	"NSMF, NELF, HH9"	NMDA receptor synaptonuclear signaling and neuronal migration factor	NSMF	26012	ENSG00000165802		"Hypogonadotropic hypogonadism 9 with or without anosmia, 614838 (3), Autosomal dominant"	Nsmf (MGI:1861755)			
chr9	137459398	137550665	9q34.3	9q34.3		612122	PNPLA7	Patatin-like phospholipase domain containing 7	PNPLA7	375775	ENSG00000130653			Pnpla7 (MGI:2385325)			
chr9	137551856	137552554	9q34.3	9q34.3		611846	"MRPL41, MRPL27"	Mitochondrial ribosomal protein L41	MRPL41	64975	ENSG00000182154			Mrpl41 (MGI:1333816)			
chr9	137554443	137578934	9q34.3	9q34.3		613210	WDR85	WD repeat-containing protein 85	DPH7	92715	ENSG00000148399			Dph7 (MGI:1914478)			
chr9	137582078	137590484	9q34.3	9q34.3		611424	"ZMYND19, MIZIP"	Zinc finger MYND domain-containing protein 19	ZMYND19	116225	ENSG00000165724			Zmynd19 (MGI:1914437)			
chr9	137618991	137836126	9q34.3	9q34.3		607001	"EHMT1, EUHMTASE1, DEL9q34, KLEFS1"	Euchromatic histone methyltransferase 1	EHMT1	79813	ENSG00000181090		"Kleefstra syndrome 1, 610253 (3), Autosomal dominant"	Ehmt1 (MGI:1924933)			
chr9	137877788	138124623	9q34	9q34.3		601012	"CACNA1B, CACNL1A5, DYT23"	"Calcium channel, voltage-dependent, L type, alpha 1B subunit"	CACNA1B	774	ENSG00000148408	mutation identified in 1 DYT23 family	"?Dystonia 23, 614860 (3), Autosomal dominant"	Cacna1b (MGI:88296)			
chr9	0	138394717	Chr.9			187290	H142T	"Temperature sensitivity complementation, H142"		8023							
chr10	0	39800000	10p			603188	BMIQ8	Body mass index quantitative trait locus 8		56694			"{Obesity, susceptibility to, BMIQ8}, 603188 (2)"				
chr10	0	39800000	10p			607499	BULN	"Bulimia nervosa, susceptibility to"		337893		between D10S1430 and D10S1423	"{Bulimia nervosa, susceptibility to}, 607499 (2), Multifactorial"				
chr10	0	6600000	10p15			611384	PFFE1	Plasmodium falciparum fever episodes QTL1		101910199			"{Plasmodium falciparum fever episodes QTL1}, 611384 (2)"				
chr10	0	51100000	10pter-q11			601188	"ST12, PAC1"	"Suppression of tumorigenicity 12, prostate"					"Prostate adenocarcinoma, 601188 (2)"				
chr10	46436	49503	10p15.3	10p15.3		616768	"TUBB8, OOMD2"	"Tubulin, beta 8"	TUBB8	347688	ENSG00000261456		"Oocyte maturation defect 2, 616780 (3), Autosomal recessive, Autosomal dominant"				
chr10	134339	254636	10p14	10p15.3		608668	"ZMYND11, BS69, BRAM1, MRD30"	Zinc finger MYND domain-containing protein 11	ZMYND11	10771	ENSG00000015171		"Mental retardation, autosomal dominant 30, 616083 (3), Autosomal dominant"	Zmynd11 (MGI:1913755)			
chr10	274189	689709	10p15.3	10p15.3		611380	"DIP2C, KIAA0934"	"Disco-interacting protein 2, Drosophila, homolog of, C"	DIP2C	22982	ENSG00000151240			Dip2c (MGI:1920179)			
chr10	806913	931899	10p15.3	10p15.3		616513	"LARP4B, LARP5, KIAA0217"	"La ribonucleoprotein domain family, member 4B"	LARP4B	23185	ENSG00000107929			Larp4b (MGI:106330)			
chr10	1018906	1025858	10p15	10p15.3		615389	"IDI2, IPPI2"	Isopentenyl-diphosphate delta isomerase 2	IDI2	91734	ENSG00000148377						
chr10	1022636	1044200	10p15	10p15.3		615391	IDI2AS1	"IDI2 antisense RNA 1, noncoding"	IDI2-AS1	55853							
chr10	1039418	1056715	10p15	10p15.3		604055	IDI1	Isopentenyl-diphosphate delta isomerase 1	IDI1	3422	ENSG00000067064			Idi1 (MGI:2442264)			
chr10	1177312	1737475	10p15	10p15.3		602065	"ADARB2, RED2"	"Adenosine deaminase, RNA-specific, B2 (homolog of rat BLUE)"	ADARB2	105	ENSG00000185736			Adarb2 (MGI:2151118)			
chr10	3067474	3136804	10p15.3-p15.2	10p15.2		171840	PFKP	"Phosphofructokinase, platelet type"	PFKP	5214	ENSG00000067057			Pfkp (MGI:1891833)			
chr10	3775995	3785280	10p15	10p15.2		602053	"KLF6, COPEB, BCD1, ZF9"	Kruppel-like factor-6	KLF6	1316	ENSG00000067082		"Gastric cancer, somatic, 613659 (3); Prostate cancer, somatic, 176807 (3)"	Klf6 (MGI:1346318)			
chr10	3800000	6600000	10p15.1			612594	MS2	"Multiple sclerosis, susceptibility to, 2"		100271694		associated with rs12722489 and rs2104286	"{Multiple sclerosis, susceptibility to, 2}, 612594 (2)"				
chr10	4824553	4908420	10p15.1	10p15.1		617451	"AKR1E2, HTSP, TAKR"	"Aldo-keto reductase family 1, member E2"	AKR1E2	83592	ENSG00000165568			Akr1e1 (MGI:1914758)			
chr10	4963261	4979966	10p15-p14	10p15.1		600449	"AKR1C1, DDH1, DD1, HAKRC"	"Aldo-keto reductase family 1, member 1 (dihydrodiol dehydrogenase, type 1)"	AKR1C1	1645	ENSG00000187134			Akr1c21 (MGI:1924587)			
chr10	4987774	5018032	10p15-p14	10p15.1		600450	"AKR1C2, DDH2, DD2, HAKRD, SRXY8"	"Aldo-keto reductase family 1, member C2 (dihydrodiol dehydrogenase, type II)"	AKR1C2	1646	ENSG00000151632		"Obesity, hyperphagia, and developmental delay (3); 46XY sex reversal 8, 614279 (3), Autosomal recessive"	Akr1c21 (MGI:1924587)			
chr10	5048765	5107685	10p15-p14	10p15.1		603966	"AKR1C3, HAKRB, DD3"	"Aldo-keto reductase family 1, member C3"	AKR1C3	8644	ENSG00000196139			Akr1c18 (MGI:2145420)			
chr10	5196834	5218946	10p15-p14	10p15.1		600451	"AKR1C4, CHDR, CDR, HAKRA, DD4"	"Aldo-keto reductase family 1, member C4 (chlordecone reductase)"	AKR1C4	1109	ENSG00000198610		"{46XY sex reversal 8, modifier of}, 614279 (3), Autosomal recessive"	Akr1c6 (MGI:1933427)			
chr10	5524888	5526267	10pter-p13	10p15.1		114184	CALML3	Calmodulin-like 3	CALML3	810	ENSG00000178363			Calml3 (MGI:1917655)			
chr10	5638856	5666594	10p15.1	10p15.1		615055	ASB13	Ankyrin repeat- and SOCS box-containing protein 13	ASB13	79754	ENSG00000196372			Asb13 (MGI:2145525)			
chr10	5765221	5813548	10p15	10p15.1		600767	"GDI2, RABGDIB"	GDP dissociation inhibitor 2	GDI2	2665	ENSG00000057608	pseudogene on chr.7		Gdi2 (MGI:99845)			
chr10	5889571	5937594	10p15.1	10p15.1		607222	"FBXO18, FBH1, FBX18"	F-box only protein 18	FBH1	84893	ENSG00000134452			Fbxo18 (MGI:1354699)			
chr10	5948896	5978740	10p15-p14	10p15.1		601070	IL15RA	"Interleukin-15 receptor, alpha"	IL15RA	3601	ENSG00000134470			Il15ra (MGI:104644)			
chr10	6010693	6062369	10p15.1	10p15.1		147730	"IL2RA, CD25, IL2R, IDDM10, IMD41"	"Interleukin-2 receptor, alpha"	IL2RA	3559	ENSG00000134460		"{Diabetes, mellitus, insulin-dependent, susceptibility to, 10}, 601942 (3); Immunodeficiency 41 with lymphoproliferation and autoimmunity, 606367 (3), Autosomal recessive"	Il2ra (MGI:96549)			
chr10	6088985	6117458	10p15.1	10p15.1		606935	"RBM17, SPF45"	RNA binding motif protein 17	RBM17	84991	ENSG00000134453			Rbm17 (MGI:1924188)			
chr10	6144877	6254647	10p15-p14	10p15.1		605319	"PFKFB3, IPFK2"	"6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3"	PFKFB3	5209	ENSG00000170525			Pfkfb3 (MGI:2181202)			
chr10	6393037	6580645	10p15	10p15.1		600448	PRKCQ	"Protein kinase C, theta"	PRKCQ	5588	ENSG00000065675			Prkcq (MGI:97601)			
chr10	6600000	29300000	10p14-p12			604401	ARVD6	Arrhythmogenic right ventricular dysplasia 6		27038			"Arrhythmogenic right ventricular dysplasia 6, 604401 (2)"				
chr10	6600000	12200000	10p14			612230	CRCS5	"Colorectal cancer, susceptibility to, 5"		100188887		associated with rs10795668	"{Colorectal cancer, susceptibility to, 5}, 612230 (2)"				
chr10	6600000	17300000	10p14-p13			601362	"DGCR2, DGS2"	DiGeorge syndrome chromosome region-2		8026			"DiGeorge syndrome/velocardiofacial syndrome complex-2, 601362 (2)"				
chr10	7158623	7411485	10p14	10p14		615392	"SFMBT2, KIAA1617"	SCM-like protein with 4 MBT domains 2	SFMBT2	57713	ENSG00000198879			Sfmbt2 (MGI:2447794)			
chr10	7559269	7666997	10p15	10p14		609783	ITIH5	"Inter-alpha-trypsin inhibitor, heavy chain 5"	ITIH5	80760	ENSG00000123243			Itih5 (MGI:1925751)			
chr10	7703272	7749519	10p15	10p14		146640	ITIH2	"Inter-alpha (globulin) inhibitor, H2 polypeptide"	ITIH2	3698	ENSG00000151655			Itih2 (MGI:96619)			
chr10	7750961	7788026	10p15-p14	10p14		601720	"KIN, KIN17, BTCD"	"Antigenic determinant of recombination protein A, mouse, homolog of"	KIN	22944	ENSG00000151657			Kin (MGI:96676)			
chr10	7788103	7807800	10p15.1	10p14		108729	"ATP5C1, ATP5CL1, ATP5C"	"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide-1"	ATP5F1C	509	ENSG00000165629			Atp5c1 (MGI:1261437)			
chr10	7818503	8016630	10p14	10p14		606576	"TAF3, TAFII140"	"TAF3 RNA polymerase II, TATA box-binding protein-associated factor, 140kD"	TAF3	83860	ENSG00000165632			Taf3 (MGI:2388097)			
chr10	8045419	8075200	10p15	10p14		131320	"GATA3, HDR, HDRS"	GATA-binding protein-3	GATA3	2625	ENSG00000107485		"Hypoparathyroidism, sensorineural deafness, and renal dysplasia, 146255 (3), Autosomal dominant"	Gata3 (MGI:95663)			
chr10	10462514	11336674	10p13	10p14		602538	"CELF2, CUGBP2, ETR3, BRUNOL3"	"CUGbp- and ELAV-like family, member 2"	CELF2	10659	ENSG00000048740			Celf2 (MGI:1338822)			
chr10	11460509	11611788	10p13	10p14		605405	"USP6NL, RNTRE"	USP6 N-terminal-like	USP6NL	9712	ENSG00000148429			Usp6nl (MGI:2138893)			
chr10	11920021	12043169	10p15-p13	10p14		605529	"UPF2, RENT2"	"UPF2 regulator of nonsense transcripts, yeast, homolog of"	UPF2	26019	ENSG00000151461			Upf2 (MGI:2449307)			
chr10	12068916	12123227	10p14	10p14		614984	"DHTKD1, KIAA1630, AMOXAD, CMT2Q"	Dehydrogenase E1 and transketolase domains-containing protein 1	DHTKD1	55526	ENSG00000181192	mutation identified in 1 CMT2Q family	"2-aminoadipic 2-oxoadipic aciduria, 204750 (3), Autosomal recessive; ?Charcot-Marie-Tooth disease, axonal, type 2Q, 615025 (3), Autosomal dominant"	Dhtkd1 (MGI:2445096)			
chr10	12195961	12250589	10p14-p13	10p14-p13		617708	CDC123	Cell division cycle 123	CDC123	8872	ENSG00000151465			Cdc123 (MGI:2138811)			
chr10	12200000	17300000	10p13			606187	AD7	Alzheimer disease 7		114475		max LOD at D10S1423	"Alzheimer disease-7, 606187 (2)"				
chr10	12200000	17300000	10p13			609888	LPRS	"Leprosy, paucibacillary type, susceptibility to"		81861			"{Leprosy, paucibacillary type, susceptibility to}, 609888 (2)"				
chr10	12349513	12835544	10p13	10p13		607957	"CAMK1D, CKLIK"	Calcium/calmodulin-dependent protein kinase I-delta	CAMK1D	57118	ENSG00000183049			Camk1d (MGI:2442190)			
chr10	13100081	13138275	10p15-p14	10p13		602432	"OPTN, GLC1E, FIP2, HYPL, NRP, ALS12"	Optineurin	OPTN	10133	ENSG00000123240		"Amyotrophic lateral sclerosis 12, 613435 (3); Glaucoma 1, open angle, E, 137760 (3), Autosomal dominant; {Glaucoma, normal tension, susceptibility to}, 606657 (3)"	Optn (MGI:1918898)			
chr10	13161553	13211109	10p13	10p13		609357	"MCM10, CNA43"	"Minichromosome maintenance 10, S. cerevisiae, homolog of"	MCM10	55388	ENSG00000065328			Mcm10 (MGI:1917274)			
chr10	13277795	13300129	10pter-p11.2	10p13		602026	"PHYH, PAHX"	Phytanoyl-CoA hydroxylase	PHYH	5264	ENSG00000107537		"Refsum disease, 266500 (3), Autosomal recessive"	Phyh (MGI:891978)			
chr10	13317427	13348297	10p13	10p13		600902	"SEPHS1, SPS1"	Selenophosphate synthetase 1	SEPHS1	22929	ENSG00000086475			Sephs1 (MGI:1923580)			
chr10	13586810	13645343	10p13	10p13		604993	"PRPF18, PRP18"	"Prp18, S. cerevisiae, homolog of"	PRPF18	8559	ENSG00000165630			Prpf18 (MGI:1914479)			
chr10	13638299	14330883	10p13	10p13		616305	"FRMD4A, KIAA1294, CCAFCA"	FERM domain-containing protein 4A	FRMD4A	55691	ENSG00000151474	mutation identified in 1 CCAFCA family	"?Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia, 616819 (3), Autosomal recessive"	Frmd4a (MGI:1919850)			
chr10	14819244	14838072	10p13	10p13		611233	"ARMETL1, CDNF"	Arginine-rich protein mutated in early stage tumors-like 1	CDNF	441549	ENSG00000185267			Cdnf (MGI:3606576)			
chr10	14838159	14871740	10p12.3	10p13		610369	"HSPA14, HSP70L1"	Heat-shock 70kD protein 14	HSPA14	51182	ENSG00000187522			Hspa14 (MGI:1354164)			
chr10	14878782	14904314	10p13	10p13		606503	"SUV39H2, FLJ23414"	"Suppressor of variegation 3-9, Drosophila, homolog of, 2"	SUV39H2	79723	ENSG00000152455			Suv39h2 (MGI:1890396)			
chr10	14897563	14954431	10p	10p13		605988	"DCLRE1C, ARTEMIS, SCIDA"	DNA cross-link repair protein 1C	DCLRE1C	64421	ENSG00000152457		"Omenn syndrome, 603554 (3), Autosomal recessive; Severe combined immunodeficiency, Athabascan type, 602450 (3), Autosomal recessive"	Dclre1c (MGI:2441769)			
chr10	14954227	14988049	10p13	10p13		614174	MEIG1	"Meiosis-expressed gene 1, mouse, homolog of"	MEIG1	644890	ENSG00000197889			Meig1 (MGI:1202878)			
chr10	15097179	15104256	10p13	10p13		606116	RPP38	"Ribonuclease P, 38-kD subunit"	RPP38	10557	ENSG00000152464			Rpp38 (MGI:2443607)			
chr10	15104587	15168709	10p13	10p13		603801	NMT2	N-myristoyltransferase 2	NMT2	9397	ENSG00000152465			Nmt2 (MGI:1202298)			
chr10	15513948	15720334	10p13	10p13		604063	"ITGA8, RHDA1"	"Integrin, alpha-8"	ITGA8	8516	ENSG00000077943		"Renal hypodysplasia/aplasia 1, 191830 (3), Autosomal recessive"	Itga8 (MGI:109442)			
chr10	15778168	15860532	10p13	10p13		611649	"MINDY3, C10orf97, CARP"	MINDY lysine-48 deubiquitinase 3	MINDY3	80013	ENSG00000148481			Mindy3 (MGI:1914210)			
chr10	16436942	16517961	10p12	10p13		604446	PTER	Phosphotriesterase-related protein	PTER	9317	ENSG00000165983			Pter (MGI:107372)			
chr10	16513742	16522004	10p13	10p13		615227	"C1QL3, CTRP13, K100"	"Complement component 1, q subcomponent-like 3"	C1QL3	389941	ENSG00000165985			C1ql3 (MGI:2387350)			
chr10	16590615	16817453	10p13	10p13		179555	RSU1	Ras suppressor protein 1	RSU1	6251	ENSG00000148484			Rsu1 (MGI:103040)			
chr10	16823965	17130491	10p12.1	10p13		602997	"CUBN, IFCR, MGA1"	Cubilin (intrinsic factor-cobalamin receptor)	CUBN	8029	ENSG00000107611		"Megaloblastic anemia-1, Finnish type, 261100 (3), Autosomal recessive"	Cubn (MGI:1931256)			
chr10	17137335	17202070	10p15.1	10p13		602478	"TRDMT1, DMNT2"	tRNA aspartic acid methyltransferase 1 (DNA methyltransferase 2)	TRDMT1	1787	ENSG00000107614			Trdmt1 (MGI:1274787)			
chr10	17228209	17237596	10p13	10p13		193060	"VIM, CTRCT30"	Vimentin	VIM	7431	ENSG00000026025		"Cataract 30, pulverulent, 116300 (3), Autosomal dominant"	Vim (MGI:98932)			
chr10	17315413	17455965	10p12.31	10p12.33		610139	"ST8SIA6, SIAT8F"	"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6"	ST8SIA6	338596	ENSG00000148488			St8sia6 (MGI:2386797)			
chr10	17589958	17617373	10p12.33	10p12.33		610467	"HACD1, PTPLA"	3-hydroxyacyl-CoA dehydratase 1	HACD1	9200	ENSG00000165996			Hacd1 (MGI:1353592)			
chr10	17644124	17716823	10p14-p13	10p12.33		601899	STAM	Signal transducing adaptor molecule	STAM	8027	ENSG00000136738			Stam (MGI:1329014)			
chr10	17809342	17911161	10p13	10p12.33		153618	"MRC1, MMR"	"Mannose receptor, C type 1"	MRC1	4360	ENSG00000260314			Mrc1 (MGI:97142)			
chr10	18140559	18545880	10p12	10p12.33-p12.31		600003	CACNB2	"Calcium channel, voltage-dependent, beta 2 subunit"	CACNB2	783	ENSG00000165995		"Brugada syndrome 4, 611876 (3)"	Cacnb2 (MGI:894644)			
chr10	18512581	18659263	10p12.31	10p12.31		617199	NSUN6	"NOP2/SUN RNA methyltransferase family, member 6"	NSUN6	221078	ENSG00000241058			Nsun6 (MGI:1921705)			
chr10	18659334	18681638	10p12.31	10p12.31		608909	"ARL5B, ARL8"	ADP-ribosylation factor-like 5B	ARL5B	221079	ENSG00000165997			Arl5b (MGI:1923119)			
chr10	19046930	19734477	10p12.31	10p12.31		617715	"MALRD1, C10orf112, DIET1"	MAM and LDL receptor class A domain-containing protein 1	MALRD1	340895	ENSG00000204740			Malrd1 (MGI:1928271)			
chr10	19816214	20289855	10p12.3	10p12.31		606827	"PLXDC2, TEM7R"	Plexin domain containing 2	PLXDC2	84898	ENSG00000120594			Plxdc2 (MGI:1914698)			
chr10	20779972	21174186	10p13-p12	10p12.31		605491	NEBL	Nebulette	NEBL	10529	ENSG00000078114						
chr10	21496561	21496640	10p12.31	10p12.31		615202	MIR1915	Micro RNA 1915	MIR1915	100302129							
chr10	21524615	21743629	10p12	10p12.31		602409	AF10	ALL1 fused gene from chromosome 10	MLLT10	8028	ENSG00000078403	fuses with MLL and HEAB	"Leukemia, acute myeloid, 601626 (3), Autosomal dominant"	Mllt10 (MGI:1329038)			
chr10	21756547	22003762	10p12.31	10p12.31		611207	"DNAJC1, HTJ1"	"DNAJ/HSP40 homolog, subfamily C, member 1"	DNAJC1	64215	ENSG00000136770			Dnajc1 (MGI:103268)			
chr10	22208813	22209982	10p12.3	10p12.31		613249	EBLN1	Endogenous Borna-like N element-containing protein 1	EBLN1	340900	ENSG00000223601						
chr10	22316382	22320316	10p12.2	10p12.2		616700	COMMD3	COMM domain-containing protein 3	COMMD3	23412	ENSG00000148444			Commd3 (MGI:88218)			
chr10	22321209	22331484	10p13	10p12.2		164831	BMI1	Oncogene BMI-1	BMI1	648	ENSG00000168283						
chr10	22345444	22417609	10p12-p11.2	10p12.2		605730	SPAG6	Sperm-associated antigen 6	SPAG6	9576	ENSG00000077327			Spag6l (MGI:1354388)			
chr10	22534836	22714573	10p12.2	10p12.2		603140	"PIP4K2A, PI5P4KA, PIP5K2A"	"Phosphatidylinositol 5-phosphate 4-kinase, type II, alpha"	PIP4K2A	5305	ENSG00000150867			Pip4k2a (MGI:1298206)			
chr10	22928023	23038526	10p12.23	10p12.2		611226	ARMC3	Armadillo repeat-containing protein 3	ARMC3	219681	ENSG00000165309			Armc3 (MGI:1918132)			
chr10	23095497	23122012	10p12	10p12.2		613782	"MSRB2, CBS1"	Methionine sulfoxide reductase B2	MSRB2	22921	ENSG00000148450			Msrb2 (MGI:1923717)			
chr10	23192530	23194251	10p12.3	10p12.2		607194	"PTF1A, PACA, PAGEN2"	"Pancreas transcription factor 1, alpha subunit"	PTF1A	256297	ENSG00000168267		"Pancreatic agenesis 2, 615935 (3), Autosomal recessive; Pancreatic and cerebellar agenesis, 609069 (3), Autosomal recessive"	Ptf1a (MGI:1328312)			
chr10	23439268	23442380	10p12.2	10p12.2		612022	"OTUD1, DUBA7"	OTU domain-containing protein 1	OTUD1	220213	ENSG00000165312			Otud1 (MGI:1918448)			
chr10	23694726	24547847	10p12.2	10p12.2-p12.1		617367	"KIAA1217, SKT"	KIAA1217 gene	KIAA1217	56243	ENSG00000120549			Etl4 (MGI:95454)			
chr10	24583608	24725420	10p12.3	10p12.1		609870	"ARHGAP21, KIAA1424"	"GTPase-activating protein, Rho, 21"	ARHGAP21	57584	ENSG00000107863	pseudogene on chr.6		Arhgap21 (MGI:1918685)			
chr10	24848606	24952643	10p12.1	10p12.1		610751	PRTFDC1	Phosphoribosyl transferase domain-containing protein 1	PRTFDC1	56952	ENSG00000099256						
chr10	24952318	25026663	10p12.1	10p12.1		611260	"THNSL1, TSH1"	Threonine synthase-like 1	THNSL1	79896	ENSG00000185875			Thnsl1 (MGI:2139347)			
chr10	24981978	25062278	10p12.1	10p12.1		611025	"ENKUR, C10orf63"	"Enkurin, TRPC channel-interacting protein"	ENKUR	219670	ENSG00000151023			Enkur (MGI:1918483)			
chr10	25174736	25602228	10p12.1	10p12.1		614573	"GPR158, KIAA1136"	G protein-coupled receptor 158	GPR158	57512	ENSG00000151025			Gpr158 (MGI:2441697)			
chr10	25934072	26212535	10p11.1	10p12.1		606808	"MYO3A, DFNB30"	Myosin IIIA	MYO3A	53904	ENSG00000095777		"Deafness, autosomal recessive 30, 607101 (3), Autosomal recessive"	Myo3a (MGI:2183924)			
chr10	26216306	26304561	10p11.23	10p12.1		138275	GAD2	"Glutamate decarboxylase-2, pancreas"	GAD2	2572	ENSG00000136750			Gad2 (MGI:95634)			
chr10	26697423	26747245	10p12.1	10p12.1		607429	"PDSS1, TPT, COQ1, COQ10D2"	"Prenyl diphosphate synthase, subunit 1"	PDSS1	23590	ENSG00000148459		"Coenzyme Q10 deficiency, primary, 2, 614651 (3), Autosomal recessive"	Pdss1 (MGI:1889278)			
chr10	26746595	26861086	10p11.2	10p12.1		603050	ABI1	ABL-interactor 1	ABI1	10006	ENSG00000136754			Abi1 (MGI:104913)			
chr10	26938194	27100497	10p12.1	10p12.1		610855	"ANKRD26, KIAA1074, THC2"	Ankyrin repeat domain-containing protein 26	ANKRD26	22852	ENSG00000107890		"Thrombocytopenia 2, 188000 (3), Autosomal dominant"	Ankrd26 (MGI:1917887)			
chr10	27110110	27155050	10p14	10p12.1		607472	"YME1L1, YME1L, PAMP, OPA11"	Mitochondrial escape 1-like 1	YME1L1	10730	ENSG00000136758	mutation identified in1 OPA11 family	"?Optic atrophy 11, 617302 (3), Autosomal recessive"	Yme1l1 (MGI:1351651)			
chr10	27154478	27187952	10p12.1	10p12.1		608221	"MASTL, FLJ14813, GWL"	Microtubule-associated serine/threonine kinase-like	MASTL	84930	ENSG00000120539			Mastl (MGI:1914371)			
chr10	27182837	27243541	10p12.1	10p12.1		616618	"ACBD5, KIAA1996"	Acyl-CoA-binding domain-containing protein 5	ACBD5	91452	ENSG00000107897			Acbd5 (MGI:1921409)			
chr10	27398187	27414367	10p12.1	10p12.1		611791	PTCHD3	Patched domain-containing protein 3	PTCHD3	374308	ENSG00000182077			Ptchd3 (MGI:1921925)			
chr10	27504173	27542236	10p12.1	10p12.1		602207	"RAB18, WARBM3"	Ras-associated protein RAB18	RAB18	22931	ENSG00000099246		"Warburg micro syndrome 3, 614222 (3), Autosomal recessive"	Rab18 (MGI:102790)			
chr10	27672873	27745848	10p12.1	10p12.1		601332	"MKX, IFRX, IRXL1"	Mohawk homeobox	MKX	283078	ENSG00000150051			Mkx (MGI:2687286)			
chr10	27812163	27999499	10p12.1	10p12.1		615408	"ARMC4, CILD23"	Armadillo repeat-containing protein 4	ARMC4	55130	ENSG00000169126		"Ciliary dyskinesia, primary, 23, 615451 (3), Autosomal recessive"	Armc4 (MGI:1922184)			
chr10	28050992	28303065	10p12.1	10p12.1		610973	MPP7	"Membrane protein, palmitoylated 7"	MPP7	143098	ENSG00000150054			Mpp7 (MGI:1922989)			
chr10	28532587	28623111	10p12.1-p11.2	10p12.1		615049	"WAC, KIAA1844, DESSH"	WW domain-containing adaptor with coiled-coil region	WAC	51322	ENSG00000095787		"Desanto-Shinawi syndrome, 616708 (3), Autosomal dominant"	Wac (MGI:2387357)			
chr10	28677494	28682938	10p12.3-p11.2	10p12.1		604444	"BAMBI, NMA"	"BMP and activin membrane-bound inhibitor, xenopus, homolog of"	BAMBI	25805	ENSG00000095739			Bambi (MGI:1915260)			
chr10	29300000	59400000	10p11.23-q21.1			607239	DFNB33	"Deafness, autosomal recessive 33"	DFNB33	170508		prev. assignment to chr. 9 an error	"Deafness, autosomal recessive 33, 607239 (2), Autosomal recessive"				
chr10	29457337	29737000	10p11.2	10p11.23		604126	SVIL	Supervillin	SVIL	6840	ENSG00000197321			Svil (MGI:2147319)			
chr10	30012799	30115493	10p11	10p11.23		614398	"KIAA1462, JCAD"	KIAA1462 gene	JCAD	57608	ENSG00000165757			Jcad (MGI:2685174)			
chr10	30309800	30349337	10p11.23	10p11.23		613669	"MTPAP, PAPD1, SPAX4"	Mitochondrial poly(A) polymerase	MTPAP	55149	ENSG00000107951	mutation identified in 1 SPAX4 family	"?Spastic ataxia 4, autosomal recessive, 613672 (3), Autosomal recessive"	Mtpap (MGI:1914690)			
chr10	30434020	30461832	10p11.2	10p11.23		191195	"MAP3K8, COT, EST, TPL2"	Mitogen-activated protein kinase kinase kinase 8 (cancer Osaka thyroid oncogene)	MAP3K8	1326	ENSG00000107968		"Lung cancer, somatic, 211980 (3)"	Map3k8 (MGI:1346878)			
chr10	30606221	30629760	10p11.23	10p11.23		612748	LYZL2	Lysozyme-like 2	LYZL2	119180	ENSG00000151033						
chr10	31100000	34200000	10p11.22			611934	EIG5	"Epilepsy, idiopathic generalized, susceptibility to, 5"		100188861		max lod at D10S1426	"{Epilepsy, idiopathic generalized, susceptibility to, 5}, 611934 (2)"				
chr10	31307716	31320446	10p11.22	10p11.22		616915	ZEB1AS1	"ZEB1 antisense RNA 1, noncoding"	ZEB1-AS1	220930							
chr10	31318494	31529813	10p11.2	10p11.22		189909	"ZEB1, TCF8, NIL2A, PPCD3, FECD6"	Zinc finger E box-binding homeobox 1	ZEB1	6935	ENSG00000148516		"Corneal dystrophy, Fuchs endothelial, 6, 613270 (3); Corneal dystrophy, posterior polymorphous, 3, 609141 (3)"	Zeb1 (MGI:1344313)			
chr10	31805397	31928875	10p12	10p11.22		610577	ARHGAP12	Rho GTPase-activating protein 12	ARHGAP12	94134	ENSG00000165322			Arhgap12 (MGI:1922665)			
chr10	32009009	32056442	10p11.22	10p11.22		602809	"KIF5B, KNS1, UKHC"	Kinesin 1	KIF5B	3799	ENSG00000170759			Kif5b (MGI:1098268)			
chr10	32267715	32378797	10p11	10p11.22		610999	EPC1	"Enhancer of polycomb, Drosophila, homolog of, 1"	EPC1	80314	ENSG00000120616			Epc1 (MGI:1278322)			
chr10	32900317	32958364	10p11.2	10p11.22		135630	"ITGB1, FNRB"	"Integrin, beta-1 (fibronectin receptor, beta polypeptide; antigen CD29 includes MDF2, MSK12)"	ITGB1	3688	ENSG00000150093	pseudogene FNRBL on 19p		Itgb1 (MGI:96610)			
chr10	33177490	33334904	10p12	10p11.22		602069	"NRP1, NRP, VEGF165R"	Neuropilin 1	NRP1	8829	ENSG00000099250			Nrp1 (MGI:106206)			
chr10	34109559	34815324	10p11.21	10p11.22-p11.21		606745	"PARD3, PAR3"	"Partitioning-defective protein 3, C. elegans, homolog of"	PARD3	56288	ENSG00000148498			Pard3 (MGI:2135608)			
chr10	34200000	59400000	10p11.21-q21.1			614990	USH1K	"Usher syndrome, type IK"	USH1K	101180907		max lod at D10S539	"Usher syndrome, type IK, 614990 (2), Autosomal recessive"				
chr10	35008550	35126898	10p11.2-p11.1	10p11.21		603135	CUL2	Cullin 2	CUL2	8453	ENSG00000108094			Cul2 (MGI:1918995)			
chr10	35126829	35212957	10p12.1-p11.2	10p11.21		123812	CREM	cAMP-responsive element modulator	CREM	1390	ENSG00000095794			Crem (MGI:88495)			
chr10	35246980	35572669	10p11.2	10p11.21		612786	"CCNY, CFP1, CCNX, C10orf9"	Cyclin Y	CCNY	219771	ENSG00000108100			Ccny (MGI:1915224)			
chr10	35605409	35608934	10p11.21	10p11.21		611922	"GJD4, CX40.1"	"Gap junction protein, delta-4"	GJD4	219770	ENSG00000177291			Gjd4 (MGI:2444990)			
chr10	35638248	35641433	10p11.2	10p11.21		606146	FZD8	"Frizzled, Drosophila, homolog of, 8"	FZD8	8325	ENSG00000177283			Fzd8 (MGI:108460)			
chr10	37125753	37309297	10p11.21	10p11.21		610856	ANKRD30A	Ankyrin repeat domain-containing protein 30A	ANKRD30A	91074	ENSG00000148513						
chr10	37949571	37976654	10p11.2-q11.2	10p11.21		194528	"ZNF25, KOX19"	Zinc finger protein-25 (KOX 19)	ZNF25	219749	ENSG00000175395			Zfp9 (MGI:99210)			
chr10	38010482	38067833	10q11.2	10p11.1		194521	"ZNF33A, NF11A, KOX2"	Zinc finger protein-33a	ZNF33A	7581	ENSG00000189180						
chr10	38094326	38150292	10p11.1	10p11.1		616085	"ZNF37A, KOX21, ZNF37"	Zinc finger protein 37A	ZNF37A	7587	ENSG00000075407						
chr10	39800000	133797422	10q			608176	AITD4	"Autoimmune thyroid disease, susceptibility to, 4"		387581			"{Autoimmune thyroid disease, susceptibility to, 4}, 608176 (2)"				
chr10	41600000	68800000	10q11.2-q21			610926	STHAG5	"Tooth agenesis, selective, 5"		100188748		D10S604 and D10S568	"Tooth agenesis, selective, 5, 610926 (2)"				
chr10	42574168	42638836	10q11.2	10q11.21		194522	"ZNF33B, ZNF11B, KOX2"	Zinc finger protein-33b	ZNF33B	7582	ENSG00000196693						
chr10	42782505	42834936	10q11.21	10q11.21		611448	"BMS1, BMS1L, KIAA0187, ACC"	"Bms1, ribosome assembly protein, S. cerevisiae, homolog of"	BMS1	9790	ENSG00000165733	mutation identified in one ACC family	"?Aplasia cutis congenita, nonsyndromic, 107600 (3), Autosomal dominant"	Bms1 (MGI:2446132)			
chr10	43077026	43130350	10q11.2	10q11.21		164761	"RET, MEN2A, HSCR1"	RET transforming sequence; oncogene RET	RET	5979	ENSG00000165731		"Central hypoventilation syndrome, congenital, 209880 (3), Autosomal dominant; {Hirschsprung disease, susceptibility to, 1}, 142623 (3), Autosomal dominant; Medullary thyroid carcinoma, 155240 (3), Autosomal dominant; Multiple endocrine neoplasia IIA, 171400 (3), Autosomal dominant; Multiple endocrine neoplasia IIB, 162300 (3), Autosomal dominant; Pheochromocytoma, 171300 (3), Autosomal dominant"	Ret (MGI:97902)			
chr10	43138444	43185307	10q11.22	10q11.21		616616	CSGALNACT2	Chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2	55454	ENSG00000169826			Csgalnact2 (MGI:1926002)			
chr10	43194532	43266918	10q11.21	10q11.21		614531	RASFEF1A	"RASGEF domain family, member 1A"	RASGEF1A	221002	ENSG00000198915			Rasgef1a (MGI:1917977)			
chr10	43371643	43376334	10q11.21	10q11.21		616926	"FXYD4, CHIF"	FXYD domain-containing ion transport regulator 4	FXYD4	53828	ENSG00000150201			Fxyd4 (MGI:1889005)			
chr10	43385616	43409247	10q11.21-q11.22	10q11.21		601037	HNRPF	Heterogeneous nuclear ribonucleoprotein F	HNRNPF	3185	ENSG00000169813			Hnrnpf (MGI:2138741)			
chr10	43554515	43574618	10q11.2	10q11.21		601069	"ZNF239, MOK2"	Zinc finger protein-239	ZNF239	8187	ENSG00000196793	previously 19q13.2-q13.3		Zfp239 (MGI:1306812)			
chr10	43643858	43648877	10q23-q24	10q11.21		194539	"ZNF32, KOX30"	Zinc finger protein-32 (KOX30)	ZNF32	7580	ENSG00000169740			Zfp637 (MGI:2448537)			
chr10	44292087	44385096	10q11.1	10q11.21		600835	"CXCL12, SDF1"	"Chemokine, C-X-C motif, ligand 12 (stromal cell-derived factor 1)"	CXCL12	6387	ENSG00000107562		"{AIDS, resistance to}, 609423 (3)"	Cxcl12 (MGI:103556)			
chr10	44959752	44994723	10q11.21	10q11.21		610559	"RASSF4, AD037"	"Ras association domain family, member 4"	RASSF4	83937	ENSG00000107551			Rassf4 (MGI:2386853)			
chr10	44976260	44978881	10q11.21	10q11.21		611309	"C10orf10, DEPP, FIG"	Chromosome 10 open reading frame 10	DEPP1	11067	ENSG00000165507			8430408G22Rik (MGI:1918730)			
chr10	45000824	45005328	10q11.2	10q11.21		194529	"ZNF22, KOX15"	Zinc finger protein-22 (KOX15)	ZNF22	7570	ENSG00000165512			Zfp422 (MGI:1914505)			
chr10	45374165	45446120	10q11.2	10q11.21		152390	ALOX5	Arachidonate 5-lipoxygenase	ALOX5	240	ENSG00000012779		"{Asthma, diminished response to antileukotriene treatment in}, 600807 (3), Autosomal dominant; {Atherosclerosis, susceptibility to} (3)"	Alox5 (MGI:87999)			
chr10	45454584	45594905	10q11.21	10q11.21-q11.22		613335	8-Mar	Membrane-associated RING-CH finger protein 8	8-Mar	220972	ENSG00000165406			March8 (MGI:1919029)			
chr10	45727199	45792963	10q11.22	10q11.22		613631	"WASHC2C, FAM21C, VPEF, KIAA0592"	"WASH complex, subunit 2C"	WASHC2C	253725	ENSG00000172661			Washc2 (MGI:106463)			
chr10	45972452	46003741	10q11.21-q11.23	10q11.22		605034	TIMM23	"Translocase of inner mitochondrial membrane 23, Yeast, homolog of"	TIMM23	100287932	ENSG00000265354			Timm23 (MGI:1858317)			
chr10	46005087	46030713	10q11.2	10q11.22		601984	"NCOA4, ELE1, PTC3"	Nuclear receptor coactivator 4	NCOA4	8031	ENSG00000266412	fused with RET to form PTC3		Ncoa4 (MGI:1350932)			
chr10	46033304	46046268	10q11.2	10q11.22		157145	"MSMB, HPC13"	"Microseminoprotein, beta"	MSMB	4477	ENSG00000263639		"{Prostate cancer, hereditary, 13}, 611928 (3)"	Msmb (MGI:97166)			
chr10	46458547	46470693	10q11.2-q21.2	10q11.22		601790	"PPYR1, NPY4R, PP1"	Pancreatic polypeptide receptor-1	NPY4R	5540	ENSG00000204174						
chr10	46543973	46557417	10q11.22	10q11.22		611240	"GPRIN2, GRIN2"	G protein-regulated inducer of neurite outgrowth 2	GPRIN2	9721	ENSG00000204175			Gprin2 (MGI:2444560)			
chr10	46578017	46595169	10q11.1	10q11.22		608081	SYT15	Synaptotagmin 15	SYT15	83849	ENSG00000204176			Syt15 (MGI:2442166)			
chr10	46911371	47003828	10q11.2	10q11.22		610630	PTPN20A	"Protein tyrosine phosphatase, nonreceptor-type, 20A"	PTPN20	26095	ENSG00000204179			Ptpn20 (MGI:1196295)			
chr10	46911371	47003828	10q11.2	10q11.22		610631	PTPN20B	"Protein tyrosine phosphatase, nonreceptor-type, 20B"	PTPN20	26095	ENSG00000204179						
chr10	47300223	47313582	10q11.22	10q11.22		601361	"GDF10, BMP3B"	Growth/differentiation factor 10	GDF10	2662	ENSG00000266524			Gdf10 (MGI:95684)			
chr10	47322489	47327587	10q11.22	10q11.22		605120	"GDF2, BMP9, HHT5"	Growth differentiation factor 2 (bone morphogenetic protein 9)	GDF2	2658	ENSG00000263761		"Telangiectasia, hereditary hemorrhagic, type 5, 615506 (3), Autosomal dominant"	Gdf2 (MGI:1321394)			
chr10	47348370	47357874	10q11.2	10q11.22		180290	"RBP3, RP66"	"Retinol-binding protein-3, interstitial"	RBP3	5949	ENSG00000265203	1 family identified with mutation	"?Retinitis pigmentosa 66, 615233 (3), Autosomal recessive"	Rbp3 (MGI:97878)			
chr10	47467992	47991878	10q11.2	10q11.22		602396	ANXA8	Annexin A8	ANXA8	653145	ENSG00000265190			Anxa8 (MGI:1201374)			
chr10	48156558	48274897	10q11.22	10q11.22		613323	FRMPD2	FERM and PDZ domains-containing protein 2	FRMPD2	143162	ENSG00000170324			Frmpd2 (MGI:2685472)			
chr10	48306638	48439359	10q11.2	10q11.22		601158	"MAPK8, PRKM8, JNK1, SAPK1"	Mitogen-activated protein kinase 8	MAPK8	5599	ENSG00000107643			Mapk8 (MGI:1346861)			
chr10	48429830	48656264	10q11	10q11.22-q11.23		610585	ARHGAP22	Rho GTPase-activating protein 22	ARHGAP22	58504	ENSG00000128805			Arhgap22 (MGI:2443418)			
chr10	48600000	51100000	10q11.23			610987	"ASAH2C, ASAH2L"	N-acylsphingosine amidohydrolase 2C									
chr10	48600000	80300000	10q11.23-q22.3			614237	HYPT9	Hypotrichosis 9		100736250		between D10S538 and D10S2327	"Hypotrichosis 9, 614237 (2), Autosomal recessive"				
chr10	48684815	48982955	10q11.22-q11.23	10q11.23		613316	"WDFY4, KIAA1607"	WD repeat- and FYVE domain-containing protein 4	WDFY4	57705	ENSG00000128815			Wdfy4 (MGI:3584510)			
chr10	49364069	49396015	10q11.23	10q11.23		606701	"DRGX, DRG11"	Dorsal root ganglia homeobox	DRGX	644168	ENSG00000165606						
chr10	49454479	49539537	10q11	10q11.23		609413	"ERCC6, CKN2, COFS1, CSB, ARMD5, UVSS1, POF11"	"Excision repair cross complementing rodent repair deficiency, complementation group 6"	ERCC6	2074	ENSG00000225830		"Cerebrooculofacioskeletal syndrome 1, 214150 (3), Autosomal recessive; Cockayne syndrome, type B, 133540 (3), Autosomal recessive; De Sanctis-Cacchione syndrome, 278800 (3), Autosomal recessive; {Lung cancer, susceptibility to}, 211980 (3), Autosomal recessive; {Macular degeneration, age-related, susceptibility to, 5}, 613761 (3); Premature ovarian failure 11, 616946 (3), Autosomal dominant; UV-sensitive syndrome 1, 600630 (3), Autosomal recessive"	Ercc6 (MGI:1100494)			
chr10	49609094	49665103	10q11.2	10q11.23		118490	"CHAT, CMS6"	Choline acetyltransferase	CHAT	1103	ENSG00000070748		"Myasthenic syndrome, congenital, 6, presynaptic, 254210 (3), Autosomal recessive"	Chat (MGI:88392)			
chr10	49610300	49612719	10q11.2	10q11.23		600336	"SLC18A3, VACHT, CMS21"	"Solute carrier family 18 (vesicular acetylcholine), member 3"	SLC18A3	6572	ENSG00000187714		"Myasthenic syndrome, congenital, 21, presynaptic, 617239 (3), Autosomal recessive"	Slc18a3 (MGI:1101061)			
chr10	49734640	49762378	10q11.23	10q11.23		617513	"OGDHL, KIAA1290"	Oxoglutarate dehydrogenase-like protein	OGDHL	55753	ENSG00000197444			Ogdhl (MGI:3616088)			
chr10	49818273	49942026	10q11.23	10q11.23		603501	PARG	Poly(ADP-ribose) glycohydrolase	PARG	8505	ENSG00000227345			Parg (MGI:1347094)			
chr10	50184860	50251563	10q11.23	10q11.23		611202	ASAH2	N-acylsphingosine amidohydrolase 2	ASAH2	56624	ENSG00000188611			Asah2 (MGI:1859310)			
chr10	50305584	50623976	10q11.2	10q11.23		611573	"SGMS1, SMS1, TMEM23, MOB"	Sphingomyelin synthase 1	SGMS1	259230	ENSG00000198964			Sgms1 (MGI:2444110)			
chr10	50991150	52298349	10q11.2	10q11.2-q21.1		176894	"PRKG1, PRKG1B, PRKGR1B, AAT8"	"Protein kinase, cGMP-dependent, regulatory, type I"	PRKG1	5592	ENSG00000185532		"Aortic aneurysm, familial thoracic 8, 615436 (3), Autosomal dominant"	Prkg1 (MGI:108174)			
chr10	51100000	68800000	10q21			613065	ALL1	"Leukemia, acute lymphocytic, susceptibility to, 1"		100310785		associated with rs10821936	"{Leukemia, acute lymphocytic, susceptibility to, 1}, 613065 (2)"				
chr10	51100000	68800000	10q21			612369	ALPQTL4	"Alkaline phosphatase, plasma level of, QTL 4"		100196916		linkage with rs12355784	"{Alkaline phosphatase, plasma level of, QTL4}, 612369 (2)"				
chr10	51100000	68800000	10q21			612255	IBD15	Inflammatory bowel disease 15		100190929		association with rs10761659	"{Inflammatory bowel disease 15}, 612255 (2)"				
chr10	51100000	68800000	10q21			612357	MAFD8	Major affective disorder 8		100196912		associated with rs20994336	"{Major affective disorder-8, susceptibility to}, 612357 (2)"				
chr10	51100000	59400000	10q21.1			612717	MYP15	Myopia 15	MYP15	100294716		max lod at D10S1643	"Myopia 15, 612717 (2), Autosomal dominant"				
chr10	51695485	51699594	10q22-q23	10q21.1		611968	"CSTF2T, KIAA0689"	"Cleavage stimulation factor, 3-prime pre-RNA, subunit 2, 64kD, tau variant"	CSTF2T	23283	ENSG00000177613			Cstf2t (MGI:1932622)			
chr10	52314182	52317656	10q11.2	10q21.1		605189	DKK1	"Dickkopf, Xenopus, homolog of, 1"	DKK1	22943	ENSG00000107984			Dkk1 (MGI:1329040)			
chr10	52764976	52772846	10q11.2-q21	10q21.1		154545	"MBL2, MBL, MBP1, MBL2D, MBPD"	"Mannose-binding lectin 2, soluble (opsonic defect)"	MBL2	4153	ENSG00000165471	near MEN2A	"{Chronic infections, due to MBL deficiency}, 614372 (3), Autosomal dominant"	Mbl2 (MGI:96924)			
chr10	53802770	55629181	10q21-q22	10q21.1		605514	"PCDH15, DFNB23, USH1F"	Protocadherin 15	PCDH15	65217	ENSG00000150275		"Deafness, autosomal recessive 23, 609533 (3), Autosomal recessive; Usher syndrome, type 1D/F digenic, 601067 (3), Autosomal recessive, Digenic recessive; Usher syndrome, type 1F, 602083 (3), Autosomal recessive"	Pcdh15 (MGI:1891428)			
chr10	56357437	56361272	10q21-q22	10q21.1		609177	"ZWINT, SIP30"	ZW10 interacting kinetochore protein	ZWINT	11130	ENSG00000122952			Zwint (MGI:1289227)			
chr10	58191516	58269960	10q21	10q21.1		609851	IPMK	Inositol polyphosphate multikinase	IPMK	253430	ENSG00000151151			Ipmk (MGI:1916968)			
chr10	58269101	58289258	10q21.1	10q21.1		611932	"CISD1, MITONEET"	CDGSH iron sulfur domain protein 1	CISD1	55847	ENSG00000122873			Cisd1 (MGI:1261855)			
chr10	58334978	58370752	10q11.2-q21	10q21.1		602961	"UBE2D1, UBCH5A, UBCH5"	Ubiquitin-conjugating enzyme E2D 1	UBE2D1	7321	ENSG00000072401			Ube2d1 (MGI:2384911)			
chr10	58385142	58399229	10q21	10q21.1		600438	"TFAM, TCF6L2, TCF6L1, TCF6L3, MTTF1, TCF6, MTDPS15"	"Transcription factor A, mitochondrial"	TFAM	7019	ENSG00000108064	mutation identified in 1 MTDPS15 family	"?Mitochondrial DNA depletion syndrome 15 (hepatocerebral type), 617156 (3), Autosomal recessive"	Tfam (MGI:107810)			
chr10	58512902	58831436	10q21.2	10q21.1		614295	"BICC1, BICC, CYSRD"	"Bicaudal C, Drosophila, homolog of, 1"	BICC1	80114	ENSG00000122870		"{Renal dysplasia, cystic, susceptibility to}, 601331 (3), Autosomal dominant"	Bicc1 (MGI:1933388)			
chr10	59650763	59710078	10q21.2	10q21.2		614242	"SLC16A9, MCT9"	"Solute carrier family 16 (monocarboxylic acid transporter), member 9"	SLC16A9	220963	ENSG00000165449			Slc16a9 (MGI:1914109)			
chr10	59736989	59753444	10q21.2	10q21.2		616246	"MRLN, LINC00948"	Myoregulin	MRLN	100507027	ENSG00000227877						
chr10	59788746	59906655	10q21	10q21.2		601985	"CCDC6, D10S170, H4, TST1"	Coiled-coil domain-containing 6	CCDC6	8030	ENSG00000108091	fused with RET to form PTC1		Ccdc6 (MGI:1923801)			
chr10	60026297	60733525	10q21	10q21.2		600465	"ANK3, MRT37"	"Ankyrin-3, node of Ranvier"	ANK3	288	ENSG00000151150	mutation identified in 1 family	"?Mental retardation, autosomal recessive, 37, 615493 (3), Autosomal recessive"	Ank3 (MGI:88026)			
chr10	60778330	60794851	10q21.1	10q21.2		116940	"CDK1, CDC2"	Cyclin-dependent kinase 1	CDK1	983	ENSG00000170312			Cdk1 (MGI:88351)			
chr10	60869437	61001485	10q21.1	10q21.2		607351	"RHOBTB1, KIAA0740"	Rho-related BTB domain-containing protein 1	RHOBTB1	9886	ENSG00000072422			Rhobtb1 (MGI:1916538)			
chr10	61406641	61453449	10q21.2	10q21.2		617803	TMEM26	Transmembrane protein 26	TMEM26	219623	ENSG00000196932			Tmem26 (MGI:2143537)			
chr10	61901253	62096947	10q21.2	10q21.2		608538	"ARID5B, MRF2, DESRT"	AT-rich interaction domain-containing protein 5B	ARID5B	84159	ENSG00000150347			Arid5b (MGI:2175912)			
chr10	62374156	62672010	10q21.2	10q21.2		607818	"ZNF365, UAN"	Zinc finger protein 365	ZNF365	22891	ENSG00000138311		"{Nephrolithiasis, uric acid, susceptibility to}, 605990 (3)"	Zfp365 (MGI:2143676)			
chr10	62800000	73100000	10q21.3-q22.1			604185	HCFP2	"Facial paresis, hereditary congenital, 2"	MBS3	22811			"Facial paresis, hereditary congenital, 2, 604185 (2), Autosomal dominant"				
chr10	62800000	80300000	10q21.3-q22.3			613339	HWE1	"Epilepsy, hot water, 1"		100415903		max lod at D10S412	"Epilepsy, hot water, 1, 613339 (2), Autosomal dominant"				
chr10	62800000	68800000	10q21.3			614996	MSE	Myelinating Schwann cell element		101180900							
chr10	62804755	62808478	10q21.3	10q21.3		611392	"ADO, C10orf22"	2-aminoethanethiol dioxygenase	ADO	84890	ENSG00000181915			Ado (MGI:2685083)			
chr10	62811995	62819166	10q21.1-q22.1	10q21.3		129010	"EGR2, KROX20"	"KROX-20, Drosophila, homolog of (early growth response-2)"	EGR2	1959	ENSG00000122877		"Charcot-Marie-Tooth disease, type 1D, 607678 (3), Autosomal dominant; Dejerine-Sottas disease, 145900 (3), Autosomal recessive, Autosomal dominant; Neuropathy, congenital hypomyelinating, 1, 605253 (3), Autosomal recessive, Autosomal dominant"	Egr2 (MGI:95296)			
chr10	63133246	63155030	10q21.3	10q21.3		616477	"NRBF2, COPR"	Nuclear receptor-binding factor 2	NRBF2	29982	ENSG00000148572			Nrbf2 (MGI:1354950)			
chr10	63167220	63522074	10q21.3	10q21.3		604503	"JMJD1C, TRIP8, KIAA1380"	Jumonji domain-containing protein 1C	JMJD1C	221037	ENSG00000171988			Jmjd1c (MGI:1918614)			
chr10	63521352	63625122	10q21.3	10q21.3		609348	"REEP3, C10orf74"	Receptor expression-enhancing protein 3	REEP3	221035	ENSG00000165476			Reep3 (MGI:88930)			
chr10	65912517	67696216	10q21	10q21.3		607667	"CTNNA3, ARVD13"	"Catenin, alpha-3"	CTNNA3	29119	ENSG00000183230		"Arrhythmogenic right ventricular dysplasia, familial, 13, 615616 (3), Autosomal dominant"	Ctnna3 (MGI:2661445)			
chr10	66926033	67101550	10q21.3	10q21.3		610869	LRRTM3	Leucine-rich repeat transmembrane protein 3	LRRTM3	347731	ENSG00000198739			Lrrtm3 (MGI:2389177)			
chr10	67796664	67838186	10q21.1	10q21.3		606060	"DNAJC12, JDP1, HPANBH4"	"DNAJ/HSP40 homolog, subfamily C, member 12"	DNAJC12	56521	ENSG00000108176		"Hyperphenylalaninemia, mild, non-BH4-deficient, 617384 (3), Autosomal recessive"	Dnajc12 (MGI:1353428)			
chr10	67884668	67918389	10q21.3	10q21.3		604479	"SIRT1, SIR2L1"	"Sirtuin, S. cerevisiae, homolog 1"	SIRT1	23411	ENSG00000096717			Sirt1 (MGI:2135607)			
chr10	68087906	68212016	10q21.1	10q21.3		608517	"MYPN, CMD1DD, CMH22, RCM4, NEM11"	Myopalladin	MYPN	84665	ENSG00000138347		"Cardiomyopathy, dilated, 1KK, 615248 (3), Autosomal dominant; Cardiomyopathy, familial restrictive, 4, 615248 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 22, 615248 (3), Autosomal dominant; Nemaline myopathy 11, autosomal recessive, 617336 (3), Autosomal recessive"	Mypn (MGI:1916052)			
chr10	68230594	68232112	10q21.3-q22.1	10q21.3		609875	"ATOH7, PHPVAR, NCRNA"	"Atonal, Drosophila, homolog of, 7"	ATOH7	220202	ENSG00000179774		"Persistent hyperplastic primary vitreous, autosomal recessive, 221900 (3), Autosomal recessive"	Atoh7 (MGI:1355553)			
chr10	68282659	68332957	10q21.1	10q21.3		612189	"PBLD, MAWBP, MAWDBP"	Phenazine biosynthesis-like protein domain-containing protein	PBLD	64081	ENSG00000108187			Pbld1 (MGI:1915621)			
chr10	68331692	68343195	10q22	10q21.3		602324	"HNRPH3, 2H9"	Heterogeneous nuclear ribonucleoprotein H3	HNRNPH3	3189	ENSG00000096746			Hnrnph3 (MGI:1926462)			
chr10	68341106	68407301	10q21.1	10q21.3		610328	"RUFY2, KIAA1537"	RUN and FYVE domains-containing protein 2	RUFY2	55680	ENSG00000204130			Rufy2 (MGI:1917682)			
chr10	68414063	68472520	10q21.3-q22.1	10q21.3		601810	"DNA2, DNA2L, KIAA0083, PEOA6, SCKL8"	"DNA replication helicase 2, yeast, homolog of"	DNA2	1763	ENSG00000138346	mutation identified in 1 SCKL8 family	"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6, 615156 (3), Autosomal dominant; ?Seckel syndrome 8, 615807 (3), Autosomal recessive"	Dna2 (MGI:2443732)			
chr10	68482332	68527522	10q21.3-q22.1	10q21.3		139080	"SLC25A16, D10S105E, GDA"	"Solute carrier family 25 (mitochondrial carrier), member 16 (Graves disease autoantigen)"	SLC25A16	8034	ENSG00000122912			Slc25a16 (MGI:1920382)			
chr10	68560359	68700793	10q22	10q21.3		607790	"TET1, CXXC6, LCX, KIAA1676"	tet oncogene 1	TET1	80312	ENSG00000138336			Tet1 (MGI:1098693)			
chr10	68721143	68792376	10q21.3	10q21.3		612569	"CCAR1, CARP1"	Cell division cycle and apoptosis regulator 1	CCAR1	55749	ENSG00000060339			Ccar1 (MGI:1914750)			
chr10	68800000	104000000	10q22-q24			608583	ATFB1	"Atrial fibrillation, familial, 1"		406216			"Atrial fibrillation, familial, 1, 608583 (2), Autosomal dominant"				
chr10	68800000	95300000	10q22-q23			611706	MGR12	"Migraine, with or without aura, susceptibility to, 12"		100188851		max lod at 100cM	"{Migraine, with or without aura, susceptibility to, 12}, 611706 (2), Autosomal dominant"				
chr10	68800000	97500000	10q22.1-q24.1			609041	SPG27	"Spastic paraplegia-27, autosomal recessive"	SPG27	414886		between  D10S606 and D10S1758	"Spastic paraplegia 27, autosomal recessive, 609041 (2), Autosomal recessive"				
chr10	68800000	80300000	10q22			611003	SQTL1	Smoking as a quantitative trait locus 1		100188827		near D10S1432	"{Smoking as a quantitative trait locus 1}, 611003 (2)"				
chr10	68827536	68895941	10q22.1	10q22.1		609397	"STOX1, PEE4"	Storkhead box 1	STOX1	219736	ENSG00000165730		"Preeclampsia/eclampsia 4, 609404 (3)"	Stox1 (MGI:2684909)			
chr10	68898816	68956311	10q22.1	10q22.1		610373	"DDX50, GUB"	DEAD/H box 50	DDX50	79009	ENSG00000107625			Ddx50 (MGI:2182303)			
chr10	68956122	68985068	10q21	10q22.1		606357	DDX21	DEAD/H box 21	DDX21	9188	ENSG00000165732			Ddx21 (MGI:1860494)			
chr10	68988720	69016982	10q22.1	10q22.1		609367	KIAA1279	KIAA1279 gene	KIF1BP	26128	ENSG00000198954		"Goldberg-Shprintzen megacolon syndrome, 609460 (3), Autosomal recessive"	Kif1bp (MGI:1919570)			
chr10	69057532	69104810	10q22.1	10q22.1		177040	"SRGN, PRG1, PRG"	Serglycin	SRGN	5552	ENSG00000122862						
chr10	69124152	69174415	10q21.1	10q22.1		605506	"VPS26A, VPS26, HB58"	"Vacuolar protein sorting 26, yeast, homolog of, A"	VPS26A	9559	ENSG00000122958			Vps26a (MGI:1353654)			
chr10	69180203	69209097	10q22.1	10q22.1		605122	SUPV3L1	Suv3-like 1	SUPV3L1	6832	ENSG00000156502			Supv3l1 (MGI:2441711)			
chr10	69220302	69267558	10q22.1	10q22.1		617221	HKDC1	Hexokinase domain-containing protein 1	HKDC1	80201	ENSG00000156510			Hkdc1 (MGI:2384910)			
chr10	69269990	69401881	10q22	10q22.1		142600	"HK1, HKD, HMSNR, RP79"	Hexokinase-1	HK1	3098	ENSG00000156515	10p11.2 conflicting assignment; ?2 loci on chr.10	"Hemolytic anemia due to hexokinase deficiency, 235700 (3), Autosomal recessive; Neuropathy, hereditary motor and sensory, Russe type, 605285 (3), Autosomal recessive; Retinitis pigmentosa 79, 617460 (3), Autosomal dominant"	Hk1 (MGI:96103)			
chr10	69404201	69416917	10q11-q21	10q22.1		162321	"TACR2, TAC2R, NKNAR"	Tachykinin receptor 2 (substance K receptor; neurokinin 2 receptor)	TACR2	6865	ENSG00000075073			Tacr2 (MGI:98477)			
chr10	69451463	69549507	10q22.1	10q22.1		613140	"TSPAN15, NET7"	Tetraspanin 15	TSPAN15	23555	ENSG00000099282			Tspan15 (MGI:1917673)			
chr10	69571439	69573453	10q21.3	10q22.1		604882	"NEUROG3, NGN3, ATOH5"	Neurogenin 3	NEUROG3	50674	ENSG00000122859		"Diarrhea 4, malabsorptive, congenital, 610370 (3), Autosomal recessive"	Neurog3 (MGI:893591)			
chr10	69801834	69959147	10q22	10q22.1		120350	"COL13A1, CMS19"	"Collagen XIII, alpha-1 polypeptide"	COL13A1	1305	ENSG00000197467	~550kb proximal to P4HA	"Myasthenic syndrome, congenital, 19, 616720 (3), Autosomal recessive"	Col13a1 (MGI:1277201)			
chr10	70052600	70112283	10q22.3	10q22.1		616141	H2AFY2	"H2A histone family, member Y2"	H2AFY2	55506	ENSG00000099284			H2afy2 (MGI:3037658)			
chr10	70137980	70146739	10q22.1	10q22.1		611017	TYSND1	Trypsin domain-containing protein 1	TYSND1	219743	ENSG00000156521			Tysnd1 (MGI:1919017)			
chr10	70150203	70170528	10q22.1	10q22.1		607691	"SARA1, SAR1A"	"Sar1a, S. cerevisiae, homolog 1"	SAR1A	56681	ENSG00000079332			Sar1a (MGI:98230)			
chr10	70202829	70233433	10q21.3	10q22.1		179030	PP	Inorganic pyrophosphatase	PPA1	5464	ENSG00000180817			Ppa1 (MGI:97831)			
chr10	70254956	70283693	10q21	10q22.1		607448	NPFF1	Neuropeptide FF1	NPFFR1	64106	ENSG00000148734			Npffr1 (MGI:2685082)			
chr10	70404104	70428617	10q21-q22	10q22.1		602224	"EIF4EBP2, 4EBP2"	Eukaryotic translation initiation factor-4E binding protein-1	EIF4EBP2	1979	ENSG00000148730			Eif4ebp2 (MGI:109198)			
chr10	70431935	70447947	10q22.1	10q22.1		601265	"NODAL, HTX5"	"Nodal, mouse, homolog of"	NODAL	4838	ENSG00000156574		"Heterotaxy, visceral, 5, 270100 (3), Autosomal dominant"	Nodal (MGI:97359)			
chr10	70458541	70568449	10q22.1	10q22.1		614656	"KIAA1274, PALD"	"Paladin, mouse, homolog of"	PALD1	27143	ENSG00000107719			Pald1 (MGI:1351623)			
chr10	70597347	70602787	10q22	10q22.1		170280	"PRF1, HPLH2, FLH2"	Perforin	PRF1	5551	ENSG00000180644	mistakenly assigned to chr.17	"Aplastic anemia, 609135 (3); Hemophagocytic lymphohistiocytosis, familial, 2, 603553 (3), Autosomal recessive; Lymphoma, non-Hodgkin, 605027 (3)"	Prf1 (MGI:97551)			
chr10	70672505	70762440	10q22.1	10q22.1		607506	ADAMTS14	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 14"	ADAMTS14	140766	ENSG00000138316			Adamts14 (MGI:2179942)			
chr10	70771236	70785418	10q22.1	10q22.1		612640	C10orf27	chromosome 10 open reading frame 27	TBATA	219793	ENSG00000166220			Tbata (MGI:1923820)			
chr10	70815919	70881188	10q22.1	10q22.1		603729	"SGPL1, SPL, NPHS14"	Sphingosine-1-phosphate lyase 1	SGPL1	8879	ENSG00000166224		"Nephrotic syndrome 14, 617575 (3), Autosomal recessive"	Sgpl1 (MGI:1261415)			
chr10	70882279	70888785	10q22	10q22.1		126090	"PCBD1, DCOH"	Pterin-4a-carbinolamine dehydratase 1	PCBD1	5092	ENSG00000166228		"Hyperphenylalaninemia, BH4-deficient, D, 264070 (3), Autosomal recessive"	Pcbd1 (MGI:94873)			
chr10	71212534	71302878	10q21-q22	10q22.1		607870	"UNC5B, UNC5H2"	"Unc5, C. elegans, homolog of, B"	UNC5B	219699	ENSG00000107731			Unc5b (MGI:894703)			
chr10	71319252	71363389	10q22.1	10q22.1		612373	"SLC29A3, ENT3, PHID, HCLAP"	"Solute carrier family 29 (nucleoside transporter), member 3"	SLC29A3	55315	ENSG00000198246		"Histiocytosis-lymphadenopathy plus syndrome, 602782 (3), Autosomal recessive"	Slc29a3 (MGI:1918529)			
chr10	71396933	71815946	10q21-q22	10q22.1		605516	"CDH23, USH1D, DFNB12, PITA5"	Cadherin-23 (otocadherin)	CDH23	64072	ENSG00000107736	between D10S529 and D10S573	"Deafness, autosomal recessive 12, 601386 (3), Autosomal recessive; {Pituitary adenoma 5, multiple types}, 617540 (3), Autosomal dominant; Usher syndrome, type 1D, 601067 (3), Autosomal recessive, Digenic recessive; Usher syndrome, type 1D/F digenic, 601067 (3), Autosomal recessive, Digenic recessive"	Cdh23 (MGI:1890219)			
chr10	71747555	71773579	10q22.1	10q22.1		615608	"C10orf54, B7H5"	Chromosome 10 open reading frame 54	VSIR	64115	ENSG00000107738			Vsir (MGI:1921298)			
chr10	71816282	71851374	10q22.1	10q22.1		176801	"PSAP, SAP1"	Prosaposin (sphingolipid activator protein-1)	PSAP	5660	ENSG00000197746		"Combined SAP deficiency, 611721 (3), Autosomal recessive; Gaucher disease, atypical, 610539 (3); Krabbe disease, atypical, 611722 (3), Autosomal recessive; Metachromatic leukodystrophy due to SAP-b deficiency, 249900 (3), Autosomal recessive"	Psap (MGI:97783)			
chr10	71964361	72013563	10q22.1	10q22.1		603799	"CHST3, C6ST, C6ST1, HSD"	Carbohydrate sulfotransferase 3	CHST3	9469	ENSG00000122863		"Spondyloepiphyseal dysplasia with congenital joint dislocations, 143095 (3), Autosomal recessive"	Chst3 (MGI:1858224)			
chr10	72059033	72095312	10q21-q23	10q22.1		607988	"SPOCK2, KIAA0275"	"SPARC/osteonectin, CWCV, and KAZAL-like domains proteoglycan 2"	SPOCK2	9806	ENSG00000107742			Spock2 (MGI:1891351)			
chr10	72096031	72218776	10q22.1	10q22.1		614215	"ASCC1, p50, SMABF2"	"Activating signal cointegrator 1 complex, subunit 1"	ASCC1	51008	ENSG00000138303	mutation identified in 1 SMABF2 family	"Barrett esophagus/esophageal adenocarcinoma, 614266 (3); ?Spinal muscular atrophy with congenital bone fractures 2, 616867 (3), Autosomal recessive"	Ascc1 (MGI:1916340)			
chr10	72215999	72235859	10q22.1	10q22.1		613427	"ANAPC16, MSAG, C10orf104"	"Anaphase-promoting complex, subunit 16"	ANAPC16	119504	ENSG00000166295			Anapc16 (MGI:1289325)			
chr10	72273918	72276035	10q24.33	10q22.1		607729	"DDIT4, REDD1, RTP801"	DNA damage-inducible transcript 4	DDIT4	54541	ENSG00000168209			Ddit4 (MGI:1921997)			
chr10	72332829	72355148	10q22.2	10q22.1		608376	"DNAJB12, DJ10, FLJ0027"	"DNAJ, E. coli, homolog of, subfamily B, member 12"	DNAJB12	54788	ENSG00000148719			Dnajb12 (MGI:1931881)			
chr10	72367325	72626190	10q22.1	10q22.1		605084	"MICU1, CBARA1, MPXPS"	Mitochondrial calcium uptake protein 1	MICU1	10367	ENSG00000107745		"Myopathy with extrapyramidal signs, 615673 (3), Autosomal recessive"	Micu1 (MGI:2384909)			
chr10	72692130	72887693	10q22.1	10q22.1		614197	"MCU, CCDC109A"	Mitochondrial calcium uniporter	MCU	90550	ENSG00000156026			Mcu (MGI:3026965)			
chr10	72893555	72933035	10q21.3	10q22.1		609330	"OIT3, LZP"	"Oncoprotein-induced transcript 3, mouse, homolog of"	OIT3	170392	ENSG00000138315			Oit3 (MGI:1201782)			
chr10	72934761	72955043	10q22.1	10q22.1		611653	"PLA2G12B, GXIIB"	"Phospholipase A2, group XIIB"	PLA2G12B	84647	ENSG00000138308			Pla2g12b (MGI:1917086)			
chr10	73007216	73096973	10q21.3-q23.1	10q22.1		176710	"P4HA1, P4HA"	"Procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 1"	P4HA1	5033	ENSG00000122884			P4ha1 (MGI:97463)			
chr10	73134523	73168094	10q22.2	10q22.2		616464	"ECD, SGT1"	"Ecdysoneless, Drosophila, homolog of"	ECD	11319	ENSG00000122882			Ecd (MGI:1917851)			
chr10	73241953	73247330	10q22.2	10q22.2		611206	"DNAJC9, JDD1, KIAA0974"	"DNAJ/HSP40 homolog, subfamily C, member 9"	DNAJC9	23234	ENSG00000213551			Dnajc9 (MGI:1915326)			
chr10	73248842	73252692	10q22.1	10q22.2		609204	"MRPS16, COXPD2"	Mitochondrial ribosomal protein S16	MRPS16	51021	ENSG00000182180		"Combined oxidative phosphorylation deficiency 2, 610498 (3), Autosomal recessive"	Mrps16 (MGI:1913492)			
chr10	73375100	73414084	10q21.1-q21.2	10q22.2		186360	"ANXA7, SNX"	Annexin A7 (synexin)	ANXA7	310	ENSG00000138279			Anxa7 (MGI:88031)			
chr10	73423578	73433560	10q22.2	10q22.2		614773	"MSS51, ZMYND17"	"MSS51 mitochondrial translational activator, S. cerevisiae, homolog of"	MSS51	118490	ENSG00000166343			Mss51 (MGI:1922093)			
chr10	73436427	73496023	10q21-q22	10q22.2		114106	"PPP3CB, CALNB"	"Protein phosphatase-3 (formerly 2B), catalytic subunit, beta isoform (calcineurin A beta)"	PPP3CB	5532	ENSG00000107758			Ppp3cb (MGI:107163)			
chr10	73631611	73641756	10q22.1	10q22.2		605603	MYOZ1	Myozenin 1 (calsarcin 2)	MYOZ1	58529	ENSG00000177791			Myoz1 (MGI:1929471)			
chr10	73744163	73772174	10q22.2	10q22.2		607185	"SEC24C, KIAA0079"	"Sec24-related gene family, member C"	SEC24C	9632	ENSG00000176986			Sec24c (MGI:1919746)			
chr10	73801910	73811848	10q22	10q22.2		603268	NDST2	N-deacetylase/N-sulfotransferase 2	NDST2	8509	ENSG00000166507	in intron of PCDH15		Ndst2 (MGI:97040)			
chr10	73812500	73874590	10q22	10q22.2		602123	"CAMK2G, CAMKG"	Calcium/calmodulin-dependent protein kinase (CaM kinase) II gamma	CAMK2G	818	ENSG00000148660	in intron of PCDH15		Camk2g (MGI:88259)			
chr10	73909181	73917500	10q24	10q22.2		191840	"PLAU, URK, QPD, BDPLT5"	"Plasminogen activator, urokinase"	PLAU	5328	ENSG00000122861	proximal to HOX11	"{Alzheimer disease, late-onset, susceptibility to}, 104300 (3), Autosomal dominant; Quebec platelet disorder, 601709 (3), Autosomal dominant"	Plau (MGI:97611)			
chr10	73998113	74120159	10q22.1-q23	10q22.2		193065	"VCL, CMD1W, CMH15"	Vinculin	VCL	7414	ENSG00000035403		"Cardiomyopathy, dilated, 1W, 611407 (3); Cardiomyopathy, hypertrophic, 15, 613255 (3), Autosomal dominant"	Vcl (MGI:98927)			
chr10	74120011	74151084	10q22.2	10q22.2		610366	AP3M1	"Adaptor-related protein complex 3, mu-1 subunit"	AP3M1	26985	ENSG00000185009			Ap3m1 (MGI:1929212)			
chr10	74151184	74709302	10q11-q24	10q22.2		102750	ADK	Adenosine kinase	ADK	132	ENSG00000156110		"Hypermethioninemia due to adenosine kinase deficiency, 614300 (3), Autosomal recessive"	Adk (MGI:87930)			
chr10	74824926	75032622	10q22	10q22.2		605880	"KAT6B, MYST4, MORF, GTPTS"	Lysine acetyltransferase 6B	KAT6B	23522	ENSG00000156650		"Genitopatellar syndrome, 606170 (3), Autosomal dominant; SBBYSS syndrome, 603736 (3), Autosomal dominant"				
chr10	75094431	75109220	10q22.2	10q22.2		613191	"DUSP13, TMDP, MDSP"	Dual-specificity phosphatase 13	DUSP13	51207	ENSG00000079393			Dusp13 (MGI:1351599)			
chr10	75099574	75182122	10q22.2	10q22.2		611575	"SAMD8, SMSR"	Sterile alpha motif domain-containing 8	SAMD8	142891	ENSG00000156671			Samd8 (MGI:1914880)			
chr10	75210153	75231447	10q22	10q22.2		193245	VDAC2	Voltage-dependent anion channel 2	VDAC2	7417	ENSG00000165637			Vdac2 (MGI:106915)			
chr10	75279725	75401893	10q22.2	10q22.2		613902	"ZNF503, NOLZ1"	Zinc finger protein 503	ZNF503	84858	ENSG00000165655			Zfp503 (MGI:1353644)			
chr10	75431645	76557374	10q22.3	10q22.2-q22.3		614537	"C10orf11, OCA7"	Chromosome 10 open reading frame 11	LRMDA	83938	ENSG00000148655		"Albinism, oculocutaneous, type VII, 615179 (3), Autosomal recessive"	Lrmda (MGI:1923883)			
chr10	75900000	80300000	10q22.3			608078	SCZD11	"Schizophrenia susceptibility locus, chromosome 10q-related"		404686		between D10S1677 and D10S1753	"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr10	75900000	80300000	10q22.3			607965	SLEN1	"Systemic lupus erythematosus with nephritis, susceptibility to, 1"	SLEN1	192677			"{Systemic lupus erythematosus with nephritis, susceptibility to, 1}, 607965 (2)"				
chr10	75900000	80300000	10q22.3			612388	SS3	"Sarcoidosis, susceptibility to, 3"		100196919		associated with rs2789679 and rs1049550	"{Sarcoidosis, susceptibility to, 3}, 612388 (2)"				
chr10	76869600	77637968	10q22.3	10q22.3		600150	"KCNMA1, SLO, PNKD3, CADEDS"	"Potassium large conductance calcium-activated channel, subfamily M, alpha member 1 (slowpoke, Drosophila, homolog of)"	KCNMA1	3778	ENSG00000156113	mutation identified in 1 CADEDS family	"?Cerebellar atrophy, developmental delay, and seizures, 617643 (3), Autosomal recessive; Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy, 609446 (3), Autosomal dominant"	Kcnma1 (MGI:99923)			
chr10	77790786	77926589	10q23	10q22.3		604090	"DLG5, PDLG, KIAA0583"	"Discs large, Drosophila, homolog of, 5"	DLG5	9231	ENSG00000151208			Dlg5 (MGI:1918478)			
chr10	77975148	78029539	10q22.3	10q22.3		614258	"POLR3A, RPC1, RPC155, ADDH, HLD7"	"Polymerase III, RNA, subunit A"	POLR3A	11128	ENSG00000148606		"Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism, 607694 (3), Autosomal recessive"	Polr3a (MGI:2681836)			
chr10	78033759	78056812	10q22-q23	10q22.3		602412	"RPS24, DBA3"	Ribosomal protein S24	RPS24	6229	ENSG00000138326		"Diamond-blackfan anemia 3, 610629 (3), Autosomal dominant"	Rps24 (MGI:98147)			
chr10	79068993	79316527	10q22.1-q22.3	10q22.3		607159	"RAI17, KIAA1224, ZIMP10"	Retinoic acid-induced gene 17	ZMIZ1	57178	ENSG00000108175			Zmiz1 (MGI:3040693)			
chr10	79347463	79355333	10q22-q23	10q22.3		604486	"PPIF, CYP3"	"Peptidylprolyl-cis-trans-isomerase, mitochondrial"	PPIF	10105	ENSG00000108179			Ppif (MGI:2145814)			
chr10	79555851	79560460	10q22-q23	10q22.3		178642	"SFTPA2, SPA2, COLEC5"	"Surfactant, pulmonary-associated protein A2"	SFTPA2	729238	ENSG00000185303	contiguous with SFTPA1	"Pulmonary fibrosis, idiopathic, 178500 (3), Autosomal dominant"				
chr10	79610938	79615442	10q22.2-q23.1	10q22.3		178630	"SFTPA1, SFTP1"	"Surfactant, pulmonary-associated protein A1"	SFTPA1	653509	ENSG00000122852	contiguous with SFTPA2		Sftpa1 (MGI:109518)			
chr10	79937739	79982235	10q23.3	10q22.3		178635	"SFTPD, SFTP4"	"Surfactant, pulmonary-associated protein D"	SFTPD	6441	ENSG00000133661			Sftpd (MGI:109515)			
chr10	80131682	80145063	10q22.3	10q22.3		612857	PLAC9	Placenta-specific gene 9	PLAC9	219348	ENSG00000189129						
chr10	80153952	80205676	10q22.3-q23.1	10q22.3		602572	"ANXA11, ANX11, ALS23"	Annexin A11 (annexin XI)	ANXA11	311	ENSG00000122359		"Amytrophic lateral sclerosis 23, 617839 (3), Autosomal dominant"	Anxa11 (MGI:108481)			
chr10	80271819	80289677	10q22	10q22.3		610550	"MAT1A, MATA1, SAMS1"	"Methionine adenosyltransferase I, alpha"	MAT1A	4143	ENSG00000151224		"Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency, 250850 (3), Autosomal recessive, Autosomal dominant; Methionine adenosyltransferase deficiency, autosomal recessive, 250850 (3), Autosomal recessive, Autosomal dominant"	Mat1a (MGI:88017)			
chr10	80300000	104000000	10q23-q24			611920	CPROTQ	C-reactive protein QTL		100188860		max lod at D10S1239	"[C-reactive protein QTL], 611920 (2)"				
chr10	80300000	95300000	10q23			612242	"DEL10q23, C10DELq23"	Chromosome 10q22.3-q23.2 deletion syndrome					"Chromosome 10q22.3-q23.2 deletion syndrome, 612242 (4)"				
chr10	80300000	104000000	10q23-q24			612288	IBD20	Inflammatory bowel disease 20		100190788		associated with rs11190140	"{Inflammatory bowel disease 20}, 612288 (2)"				
chr10	80336012	80356786	10q23.1	10q23.1		615154	DYDC1	DPY30 domain-containing protein 1	DYDC1	143241	ENSG00000170788			Dydc1 (MGI:1916746)			
chr10	80407828	80437114	10q23.1	10q23.1		617165	"FAM213A, PAMM"	"Family with sequence similarity 213, member A"	FAM213A	84293	ENSG00000122378			Fam213a (MGI:1917814)			
chr10	81875189	82989978	10q22	10q23.1		605533	NRG3	Neuregulin 3	NRG3	10718	ENSG00000185737			Nrg3 (MGI:1097165)			
chr10	84167227	84172075	10q23.1	10q23.1		617434	HOST2	Long noncoding RNA HOST2	CERNA2	642934							
chr10	84173763	84185293	10q23.1	10q23.1		617775	"C10orf99, CSBF, AP57"	Chromosome 10 open reading frame 99	C10orf99	387695	ENSG00000188373						
chr10	84194634	84219620	10q23.1	10q23.1		609502	"CDHR1, PCDH21, PRCAD, CORD15, RP65"	"Cadherin-related family, member 1"	CDHR1	92211	ENSG00000148600		"Cone-rod dystrophy 15, 613660 (3), Autosomal recessive; Retinitis pigmentosa 65, 613660 (3), Autosomal recessive"	Cdhr1 (MGI:2157782)			
chr10	84231519	84241460	10q23.1	10q23.1		616103	"LRIT1, PAL"	"Leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein 1"	LRIT1	26103	ENSG00000148602	"REc, A"		Lrit1 (MGI:2385320)			
chr10	84243740	84259187	10q23	10q23.1		600342	"RGR, RP44"	Retinal G protein coupled receptor	RGR	5995	ENSG00000148604		"Retinitis pigmentosa 44, 613769 (3)"	Rgr (MGI:1929473)			
chr10	85599554	86366492	10q22	10q23.1-q23.2		610659	"GRID1, KIAA1220"	"Glutamate receptor, inotropic, delta 1"	GRID1	2894	ENSG00000182771			Grid1 (MGI:95812)			
chr10	86264693	86264787	10q23.2	10q23.2		611190	MIR346	Micro RNA 346	MIR346	442911							
chr10	86435255	86521815	10q23.2	10q23.2		610754	"WAPAL, KIAA0261, FOE, WAPL"	"Wings apart-like protein, Drosophila, homolog of"	WAPL	23063	ENSG00000062650			Wapl (MGI:2675859)			
chr10	86653494	86666459	10q23.2	10q23.2		606665	OPN4	Opsin 4	OPN4	94233	ENSG00000122375			Opn4 (MGI:1353425)			
chr10	86664784	86736071	10q22.2-q23.3	10q23.2		605906	"LDB3, ZASP, CYPHER, KIAA01613, MFM4, CMD1C, CMH24, LVNC3"	LIM domain binding 3	LDB3	11155	ENSG00000122367		"Cardiomyopathy, dilated, 1C, with or without LVNC, 601493 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 24, 601493 (3), Autosomal dominant; Left ventricular noncompaction 3, 601493 (3), Autosomal dominant; Myopathy, myofibrillar, 4, 609452 (3), Autosomal dominant"	Ldb3 (MGI:1344412)			
chr10	86755785	86927968	10q22.3	10q23.2		601299	"BMPR1A, ACVRLK3, ALK3"	"Bone morphogenetic protein receptor, type IA"	BMPR1A	657	ENSG00000107779		"Juvenile polyposis syndrome, infantile form, 174900 (3), Autosomal dominant; Polyposis syndrome, hereditary mixed, 2, 610069 (3); Polyposis, juvenile intestinal, 174900 (3), Autosomal dominant"	Bmpr1a (MGI:1338938)			
chr10	86955800	86963259	10q23.2-q23.3	10q23.2		602998	"SNCG, BCSG1"	"Synuclein, gamma (breast cancer-specific gene 1)"	SNCG	6623	ENSG00000173267			Sncg (MGI:1298397)			
chr10	87050201	87095046	10q23.3	10q23.2		138130	GLUD1	Glutamate dehydrogenase-1	GLUD1	2746	ENSG00000148672	pseudogene on Xq26-q28	"Hyperinsulinism-hyperammonemia syndrome, 606762 (3), Autosomal dominant"	Glud1 (MGI:95753)			
chr10	87504465	87553460	10q23	10q23.2		605391	"MINPP1, HIPER1"	Multiple inositol polyphosphate phosphatase 1	MINPP1	9562	ENSG00000107789		"Thyroid carcinoma, follicular, 188470 (3), Autosomal dominant"	Minpp1 (MGI:1336159)			
chr10	87659718	87747704	10q22-q24	10q23.2-q23.3		603005	"PAPSS2, ATPSK2, BCYM4"	3'-phosphoadenosine 5'-phosphosulfate synthase 2	PAPSS2	9060	ENSG00000198682		"Brachyolmia 4 with mild epiphyseal and metaphyseal changes, 612847 (3), Autosomal recessive"	Papss2 (MGI:1330223)			
chr10	87700000	91100000	10q23.31			613006	IDDM24	"Diabetes mellitus, insulin-dependent, 24"		100303715		associated with rs10509540	"{Diabetes mellitus, insulin-dependent, 24}, 613006 (2)"				
chr10	87700000	95300000	10q23.3			609578	RCM2	"Cardiomyopathy, familial restrictive, 2"		619468		max lod at D10S1242	"Cardiomyopathy, familial restrictive, 2, 609578 (2)"				
chr10	87751511	87841358	10q23.31	10q23.31		614452	"ATAD1, THORASE"	"ATPase family, AAA domain-containing, member 1"	ATAD1	84896	ENSG00000138138			Atad1 (MGI:1915229)			
chr10	87859160	87863436	10q23	10q23.31		612105	"KLLN, CWS4"	Killin	KLLN	100144748	ENSG00000227268		"Cowden syndrome 4, 615107 (3)"				
chr10	87863437	87971929	10q23.31	10q23.31		601728	"PTEN, MMAC1, GLM2, CWS1"	Phosphatase and tensin homolog (mutated in multiple advanced cancers 1)	PTEN	5728	ENSG00000171862		"Bannayan-Riley-Ruvalcaba syndrome, 153480 (3), Autosomal dominant; Cowden syndrome 1, 158350 (3), Autosomal dominant; Endometrial carcinoma, somatic, 608089 (3); {Glioma susceptibility 2}, 613028 (3); Lhermitte-Duclos syndrome, 158350 (3), Autosomal dominant; Macrocephaly/autism syndrome, 605309 (3), Autosomal dominant; Malignant melanoma, somatic, 155600 (3); {Meningioma}, 607174 (3), Autosomal dominant; PTEN hamartoma tumor syndrome (3); {Prostate cancer, somatic}, 176807 (3); Squamous cell carcinoma, head and neck, somatic, 275355 (3); VATER association with macrocephaly and ventriculomegaly, 276950 (3), Autosomal recessive"	Pten (MGI:109583)			
chr10	88176051	88584479	10q23.33	10q23.31		609360	"RNLS, C10orf59"	Renalase	RNLS	55328	ENSG00000184719			Rnls (MGI:1915045)			
chr10	88583276	88623160	10q23.31	10q23.31		613921	"LIPJ, LIPL1"	Lipase J	LIPJ	142910	ENSG00000204022						
chr10	88664388	88678814	10q23.31	10q23.31		601980	LIPF	"Lipase F, gastric type"	LIPF	8513	ENSG00000182333			Lipf (MGI:1914967)			
chr10	88706224	88753091	10q23.31	10q23.31		613922	"LIPK, LIPL2"	"Lipase family, member K"	LIPK	643414	ENSG00000204021			Lipk (MGI:2679259)			
chr10	88757225	88783661	10q23.31	10q23.31		613924	"LIPN, LIPL4, ARCI8, LI4"	"Lipase family, member N"	LIPN	643418	ENSG00000204020		"Ichthyosis, congenital, autosomal recessive 8, 613943 (3), Autosomal recessive"	Lipn (MGI:1917416)			
chr10	88802729	88822021	10q23.31	10q23.31		613923	"LIPM, LIPL3"	"Lipase family, member M"	LIPM	340654	ENSG00000173239			Lipm (MGI:1926003)			
chr10	88879367	88923501	10q23	10q23.31		612352	"STAMBPL1, KIAA1373"	STAM-binding protein-like 1	STAMBPL1	57559	ENSG00000138134			Stambpl1 (MGI:1923880)			
chr10	88935073	88991396	10q22-q24	10q23.31		102620	"ACTA2, ACTSA, AAT6, MYMY5"	"Actin, alpha-2, smooth muscle, aorta"	ACTA2	59	ENSG00000107796		"Aortic aneurysm, familial thoracic 6, 611788 (3), Autosomal dominant; Moyamoya disease 5, 614042 (3); Multisystemic smooth muscle dysfunction syndrome, 613834 (3), Autosomal dominant"	Acta2 (MGI:87909)			
chr10	88968428	89017060	10q24.1	10q23.31		134637	"FAS, TNFRSF6, APT1, CD95, ALPS1A"	Fas cell surface death receptor	FAS	355	ENSG00000026103		"Autoimmune lymphoproliferative syndrome, type IA, 601859 (3), Autosomal dominant; {Autoimmune lymphoproliferative syndrome}, 601859 (3), Autosomal dominant; Squamous cell carcinoma, burn scar-related, somatic (3)"	Fas (MGI:95484)			
chr10	89205936	89207313	10q23	10q23.31		604551	CH25H	Cholesterol 25-hydroxylase	CH25H	9023	ENSG00000138135			Ch25h (MGI:1333869)			
chr10	89213568	89252038	10q23.31	10q23.31		613497	"LIPA, CESD"	"Lipase A, lysosomal acid, cholesterol esterase"	LIPA	3988	ENSG00000107798	?close to GOT	"Cholesteryl ester storage disease, 278000 (3), Autosomal recessive; Wolman disease, 278000 (3), Autosomal recessive"	Lipa (MGI:96789)			
chr10	89301948	89309275	10q23.3	10q23.31		147040	"IFIT2, IFI54, G10P2"	Interferon-induced protein with tetratricopeptide repeats 2	IFIT2	3433	ENSG00000119922			Ifit2 (MGI:99449)			
chr10	89327818	89340967	10q23.3	10q23.31		604650	IFIT4	Interferon-induced protein with tetratricopeptide repeats 4	IFIT3	3437	ENSG00000119917			"Ifit3b,Ifit3 (MGI:1101055,MGI:3698419)"			
chr10	89392545	89406486	10q23.3	10q23.31		147690	"IFIT1, IFI56, G10P1, IFNAI1"	Interferon-induced protein with tetratricopeptide repeats 1	IFIT1	3434	ENSG00000185745	10q25-q26 = conflicting site		"Ifit1bl1,Ifit1bl2 (MGI:2148249,MGI:3650685)"			
chr10	89414567	89421001	10q23.31	10q23.31		616135	"IFIT5, RI58, ISG58"	Interferon-induced protein with tetratricopeptide repeats 5	IFIT5	24138	ENSG00000152778						
chr10	89430293	89536028	10q23.3	10q23.31		611910	"SLC16A12, MCT12, CTRCT47"	"Solute carrier family 16 (monocarboxylic acid transporter), member 12"	SLC16A12	387700	ENSG00000152779	mutation identified in 1 CTRCT47 family	"Cataract 47, juvenile, with microcornea, 612018 (3), Autosomal dominant"	Slc16a12 (MGI:2147716)			
chr10	89579496	89645571	10q23	10q23.31		606160	PANK1	Pantothenate kinase 1	PANK1	53354	ENSG00000152782			Pank1 (MGI:1922985)			
chr10	89592746	89592826	10q23.31	10q23.31		613189	"MIR107, MIRN107"	Micro RNA 107	MIR107	406901							
chr10	89701589	89774942	10q22-q24	10q23.31		605498	"MPHOSPH1, MPP1"	M-phase phosphoprotein 1	KIF20B	9585	ENSG00000138182			Kif20b (MGI:2444576)			
chr10	90738692	90857913	10q21-q24	10q23.31		182137	HTR7	"5-hydroxytryptamine (serotonin) receptor-7, adenylate cyclase-coupled"	HTR7	3363	ENSG00000148680			Htr7 (MGI:99841)			
chr10	90871951	90908554	10q23.31	10q23.31		606115	RPP30	"Ribonuclease P, 30kD subunit"	RPP30	10556	ENSG00000148688			Rpp30 (MGI:1859683)			
chr10	90912099	90921274	10q23.31	10q23.31		609599	"ANKRD1, CARP"	Ankyrin repeat domain-containing protein 1	ANKRD1	27063	ENSG00000148677			Ankrd1 (MGI:1097717)			
chr10	91162401	91284330	10q23.32	10q23.32		617407	PCGF5	Polycomb group ring finger protein 5	PCGF5	84333	ENSG00000180628			Pcgf5 (MGI:1923505)			
chr10	91628440	91633100	10q23-q24	10q23.32		602999	"PPP1R3C, PPP1R5"	"Phosphatase 1, regulatory subunit 3C"	PPP1R3C	5507	ENSG00000119938			Ppp1r3c (MGI:1858229)			
chr10	91923769	92030997	10q22-q23	10q23.32		605191	"BTAF1, TAFII170, TAF172, MOT1"	"BTAF1 RNA polymerase II, B-TFIID transcription factor-associated, 170kD (Mot1, S. cerevisiae, homolog of)"	BTAF1	9044	ENSG00000095564			Btaf1 (MGI:2147538)			
chr10	92046691	92291498	10q23.3	10q23.32		610606	"CPEB3, KIAA0940"	Cytoplasmic polyadenylation element-binding protein 3	CPEB3	22849	ENSG00000107864			Cpeb3 (MGI:2443075)			
chr10	92291162	92353963	10q23.3	10q23.32-q23.33		610637	5-Mar	Membrane-associated RING-CH finger protein 5	5-Mar	54708	ENSG00000198060			March5 (MGI:1915207)			
chr10	92451683	92574094	10q23-q25	10q23.33		146680	IDE	Insulin-degrading enzyme	IDE	3416	ENSG00000119912			Ide (MGI:96412)			
chr10	92593067	92655394	10q23.33	10q23.33		148760	"KIF11, KNSL1, MCLMR"	Kinesin family member 11	KIF11	3832	ENSG00000138160		"Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, 152950 (3), Autosomal dominant"	Kif11 (MGI:1098231)			
chr10	92689923	92695650	10q24	10q23.33		604420	"HHEX, PRHX, PRH"	Hematopoietically expressed homeo box	HHEX	3087	ENSG00000152804			Hhex (MGI:96086)			
chr10	92826830	93059493	10q23.33	10q23.33		609672	"EXOC6, SEC15L1, SEC15L, SEC15"	Exocyst complex component 6	EXOC6	54536	ENSG00000138190			Exoc6 (MGI:1351611)			
chr10	93061263	93068696	10q23.3	10q23.33		608428	"CYP26C1, FFDD4"	"Cytochrome P450, subfamily XXVIC, polypeptide 1"	CYP26C1	340665	ENSG00000187553		"Focal facial dermal dysplasia 4, 614974 (3), Autosomal recessive"	Cyp26c1 (MGI:2679699)			
chr10	93073474	93077883	10q23-q24	10q23.33		602239	CYP26A1	"Cytochrome p450, subfamily XXVIA, polypeptide 1"	CYP26A1	1592	ENSG00000095596			Cyp26a1 (MGI:1096359)			
chr10	93306428	93482504	10q24	10q23.33		604603	"MYOF, FER1L3"	Myoferlin	MYOF	26509	ENSG00000138119			Myof (MGI:1919192)			
chr10	93496611	93529093	10q23.33	10q23.33		610000	"CEP55, MARCH"	"Centrosomal protein, 55kD"	CEP55	55165	ENSG00000138180		"Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly, 236500 (3), Autosomal recessive"	Cep55 (MGI:1921357)			
chr10	93566177	93590071	10q23.33	10q23.33		609044	"FFAR4, O3FAR1, GPR120, PGR4, BMIQ10"	Free fatty acid receptor 4	FFAR4	338557	ENSG00000186188		"{Obesity, susceptibility to}, 607514 (3)"	Ffar4 (MGI:2147577)			
chr10	93591835	93601743	10q24	10q23.33		180250	"RBP4, RDCCAS, MCOPCB10"	"Retinol-binding protein-4, interstitial"	RBP4	5950	ENSG00000138207	just centromeric of CYP2C cluster	"Microphthalmia, isolated, with coloboma 10, 616428 (3), Autosomal dominant; Retinal dystrophy, iris coloboma, and comedogenic acne syndrome, 615147 (3), Autosomal recessive"	Rbp4 (MGI:97879)			
chr10	93612587	93665672	10q24	10q23.33		600827	"PDE6C, PDEA2, COD4"	"Phosphodiesterase-6C, cGMP-specific, cone, alpha prime"	PDE6C	5146	ENSG00000095464		"Cone dystrophy 4, 613093 (3), Autosomal recessive"	Pde6c (MGI:105956)			
chr10	93667882	93702958	10q23.33	10q23.33		608866	"C10orf4, FRA10AC1, FRA10A"	Chromosome 10 open reading frame 4	FRA10AC1	118924	ENSG00000148690			Fra10ac1 (MGI:1917817)			
chr10	93757808	93798173	10q24	10q23.33		604619	"LGI1, EPT, ETL1, ADLTE, ADPEAF"	"Leucine-rich gene, glioma-inactivated, 1"	LGI1	9211	ENSG00000108231		"Epilepsy, familial temporal lobe, 1, 600512 (3), Autosomal dominant"	Lgi1 (MGI:1861691)			
chr10	93893950	93914270	10q23.33	10q23.33		617167	"SLC35G1, POST, TMEM20, C10orf60"	"Solute carrier family 35, member G1"	SLC35G1	159371	ENSG00000176273			Slc35g1 (MGI:2444789)			
chr10	93993988	94328391	10q23	10q23.33		608414	"PLCE1, KIAA1516, NPHS3"	"Phospholipase C, epsilon-1"	PLCE1	51196	ENSG00000138193		"Nephrotic syndrome, type 3, 610725 (3), Autosomal recessive"	Plce1 (MGI:1921305)			
chr10	94314906	94362975	10q24	10q23.33		610769	"NOC3L, FAD24"	"Nucleolar complex-associated 3, S. cerevisiae, homolog of"	NOC3L	64318	ENSG00000173145			Noc3l (MGI:1932610)			
chr10	94545766	94613904	10q23.3-q24.2	10q23.33		603946	"HELLS, LSH, ICF4"	"Helicase, lymphoid-specific"	HELLS	3070	ENSG00000119969		"Immunodeficiency-centromeric instability-facial anomalies syndrome 4, 616911 (3), Autosomal recessive"	Hells (MGI:106209)			
chr10	94683493	94736189	10q23.33	10q23.33		601131	CYP2C18	"Cytochrome P450, subfamily IIC, polypeptide 18"	CYP2C18	1562	ENSG00000108242			Cyp2c55 (MGI:1919332)			
chr10	94762680	94855550	10q24.1-q24.3	10q23.33		124020	"CYP2C, CYP2C19"	"Cytochrome P450, subfamily IIC (mephenytoin 4'-hydroxylase)"	CYP2C19	1557	ENSG00000165841	4 genes in order: cen-C18-C19-C9-C8-tel	"Clopidogrel, impaired responsiveness to, 609535 (3), Autosomal recessive; Mephenytoin poor metabolizer, 609535 (3), Autosomal recessive; Omeprazole poor metabolizer, 609535 (3), Autosomal recessive; Proguanil poor metabolizer, 609535 (3), Autosomal recessive"				
chr10	94938657	94989390	10q24	10q23.33		601130	CYP2C9	"Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 9"	CYP2C9	1559	ENSG00000138109		"Tolbutamide poor metabolizer (3); Warfarin sensitivity, 122700 (3), Autosomal dominant"	"Cyp2c65,Cyp2c66 (MGI:1919553,MGI:1917138)"			
chr10	95036771	95069496	10q23.3	10q23.33		601129	CYP2C8	"Cytochrome P450, subfamily IIc, polypeptide 8"	CYP2C8	1558	ENSG00000138115		"Rhabdomyolysis, cerivastatin-induced (3)"	"Cyp2c29,Cyp2c38,Cyp2c39 (MGI:103238,MGI:1306818,MGI:1306819)"			
chr10	95237567	95291147	10q26	10q23.33		605900	"PDLIM1, CLP36, CLIM1"	PDZ and LIM domain protein 1	PDLIM1	9124	ENSG00000107438			Pdlim1 (MGI:1860611)			
chr10	95300000	104000000	10q24			605526	AD6	Alzheimer disease 6		64851			"Alzheimer disease 6, 605526 (2)"				
chr10	95300000	110100000	10q24.1-q25.1			606483	CMTDIA	"Charcot-Marie-Tooth disease, dominant intermediate A"		387574			"Charcot-Marie-Tooth disease, dominant intermediate A, 606483 (2), Autosomal dominant"				
chr10	95300000	104000000	10q24			246560	"SHFM3, SHSF3, DUP10q24, C10DUPq24"	Split-hand/foot malformation 3 (Chromosome 10q24 duplication syndrome)				contiguous gene duplication syndrome	"Split-hand/foot malformation 3, gene duplication syndrome, 246560 (4), Autosomal dominant"				
chr10	95311772	95561438	10q23.3-q24.1	10q24.1		605264	"SORBS1, SH3D5, SH3P12, KIAA1296"	Sorbin and SH3 domain containing 1	SORBS1	10580	ENSG00000095637			Sorbs1 (MGI:700014)			
chr10	95605928	95656900	10q24.3	10q24.1		138250	"ALDH18A1, PYCS, GSAS, ARCL3A, SPG9A, SPG9B, ADCL3"	"Aldehyde dehydrogenase 18 family, member A1 (1-pyrroline-5-carboxylate synthetase)"	ALDH18A1	5832	ENSG00000059573	GOT1 and GSAS in same pathway	"Cutis laxa, autosomal dominant 3, 616603 (3), Autosomal dominant; Cutis laxa, autosomal recessive, type IIIA, 219150 (3), Autosomal recessive, Isolated cases; Spastic paraplegia 9A, autosomal dominant, 601162 (3), Autosomal dominant; Spastic paraplegia 9B, autosomal recessive, 616586 (3), Autosomal recessive"	Aldh18a1 (MGI:1888908)			
chr10	95663395	95694142	10q24.1	10q24.1		613847	"TCTN3, TECT3, C10orf61, OFD4, JBTS18"	"Tectonic family, member 3"	TCTN3	26123	ENSG00000119977		"Joubert syndrome 18, 614815 (3), Autosomal recessive; Orofaciodigital syndrome IV, 258860 (3), Autosomal recessive"	Tctn3 (MGI:1914840)			
chr10	95710900	95877265	10q24	10q24.1		601752	"ENTPD1, CD39, SPG64"	Ectonucleoside triphosphate diphosphohydrolase 1 (CD39 antigen)	ENTPD1	953	ENSG00000138185		"Spastic paraplegia 64, autosomal recessive, 615683 (3), Autosomal recessive"	Entpd1 (MGI:102805)			
chr10	96128905	96205290	10q24.1	10q24.1		617733	"ZNF518A, KIAA0335"	Zinc finger protein 518A	ZNF518A	9849	ENSG00000177853			Zfp518a (MGI:1919922)			
chr10	96189170	96271575	10q23.2	10q24.1		604515	"BLNK, SLP65, AGM4"	"B-cell linker protein (SH2 domain-containing leukocyte protein, 65kD)"	BLNK	29760	ENSG00000095585	mutation identified in 1 AGM4 family	"?Agammaglobulinemia 4, 613502 (3), Autosomal recessive"	Blnk (MGI:96878)			
chr10	96304327	96338563	10q23-q24	10q24.1		187410	"DNTT, TDT"	Terminal deoxynucleotidyltransferase	DNTT	1791	ENSG00000107447			Dntt (MGI:98659)			
chr10	96343215	96359364	10q24	10q24.1		617200	"OPALIN, TMEM10, TMP10"	Oligodendrocytic myelin paranodal and inner loop protein	OPALIN	93377	ENSG00000197430			Opalin (MGI:2657025)			
chr10	96364605	96513925	10q23-q24	10q24.1		606743	"TLL2, KIAA0932"	Tolloid-like 2	TLL2	7093	ENSG00000095587			Tll2 (MGI:1346044)			
chr10	96518109	96587051	10q24.1	10q24.1		616872	"TM9SF3, SMBP"	"Transmembrane 9 superfamily, member 3"	TM9SF3	56889	ENSG00000077147			Tm9sf3 (MGI:1914262)			
chr10	96593311	96720521	10q24.1	10q24.1		607942	"PIK3AP1, BCAP, FLJ35564"	Phosphoinositide 3-kinase adaptor protein 1	PIK3AP1	118788	ENSG00000155629			Pik3ap1 (MGI:1933177)			
chr10	96832259	96986211	10q24.1	10q24.1		607698	"LCOR, MLR2, KIAA1795"	Ligand-dependent nuclear receptor corepressor	LCOR	84458	ENSG00000196233			Lcor (MGI:2443930)			
chr10	96998037	97185925	10q24.1	10q24.1		603742	"SLIT1, SLIL1, MEGF4"	"Slit, Drosophila, homolog of, 1"	SLIT1	6585	ENSG00000187122			Slit1 (MGI:1315203)			
chr10	97222172	97292672	10q24.1	10q24.1		611587	ARHGAP19	RHO GTPase-activating protein 19	ARHGAP19	84986	ENSG00000213390			Arhgap19 (MGI:1918335)			
chr10	97332496	97334700	10q24.1	10q24.1		605006	FRAT2	Frequently rearranged in advanced T-cell lymphomas 2	FRAT2	23401	ENSG00000181274			Frat2 (MGI:2673967)			
chr10	97356700	97401369	10q24.1	10q24.1		617723	"RRP12, KIAA0690"	"Ribosomal RNA-processing protein 12, S. cerevisiae, homolog of"	RRP12	23223	ENSG00000052749			Rrp12 (MGI:2147437)			
chr10	97426124	97433443	10q25.3	10q24.1		172250	PGAM1	"Phosphoglycerate mutase A, nonmuscle form"	PGAM1	5223	ENSG00000171314			Pgam1 (MGI:97552)			
chr10	97435908	97446016	10q24.1	10q24.1		606493	"EXOSC1, CSL4"	Exosome component 1	EXOSC1	51013	ENSG00000171311			Exosc1 (MGI:1913833)			
chr10	97446130	97457369	10q24	10q24.1		616750	"ZDHHC16, APH2"	Zinc finger DHHC domain-containing protein 16	ZDHHC16	84287	ENSG00000171307			Zdhhc16 (MGI:1921418)			
chr10	97458323	97498793	10q24.1	10q24.1		614777	"MMS19, MMS19L"	"MMS19 nucleotide excision repair, S. Cerevisiae, homolog of"	MMS19	64210	ENSG00000155229			Mms19 (MGI:1919449)			
chr10	97498881	97571209	10q24.1-q24.2	10q24.1-q24.2		616388	UBTD1	Ubiquitin domain-containing protein 1	UBTD1	80019	ENSG00000165886			Ubtd1 (MGI:2385092)			
chr10	97572440	97583895	10q23.31-q23.32	10q24.2		610734	"ANKRD2, ARPP"	Ankyrin repeat domain-containing protein 2	ANKRD2	26287	ENSG00000165887			Ankrd2 (MGI:1861447)			
chr10	97584344	97612801	10q24.2	10q24.2		613597	"HOGA1, DHDPSL, HP3"	4-hydroxy-2-oxoglutarate aldolase 1	HOGA1	112817	ENSG00000241935		"Hyperoxaluria, primary, type III, 613616 (3)"	Hoga1 (MGI:1914682)			
chr10	97614552	97634155	10q24.2	10q24.2		617736	"MORN4, RTP, UTA"	MORN repeat-containing protein 4	MORN4	118812	ENSG00000171160			Morn4 (MGI:2449568)			
chr10	97640685	97676433	10q24	10q24.2		609763	PI4K2A	Phosphatidylinositol 4-kinase type 2 alpha	PI4K2A	55361	ENSG00000155252			Pi4k2a (MGI:1934031)			
chr10	97713707	97718151	10q24.2	10q24.2		616970	"MARVELD1, MARVD1"	Marvel domain-containing protein 1	MARVELD1	83742	ENSG00000155254			Marveld1 (MGI:2147570)			
chr10	97737120	97760906	10q24.2	10q24.2		610243	"ZFYVE27, SPG33"	Zinc finger FYVE domain-containing protein 27	ZFYVE27	118813	ENSG00000155256		"Spastic paraplegia 33, autosomal dominant, 610244 (3), Autosomal dominant"	Zfyve27 (MGI:1919602)			
chr10	97766750	97771998	10q24.1	10q24.2		604158	"SFRP5, SARP3"	Secreted frizzled-related protein 5	SFRP5	6425	ENSG00000120057			Sfrp5 (MGI:1860298)			
chr10	97850237	97871577	10q22	10q24.2		614189	"GOLGA7B, C10orf132"	"Golgin A7 family, member B"	GOLGA7B	401647	ENSG00000155265			Golga7b (MGI:1918396)			
chr10	98247685	98268249	10q24	10q24.2		607318	LOXL4	Lysyl oxidate-like 4	LOXL4	84171	ENSG00000138131			Loxl4 (MGI:1914823)			
chr10	98383564	98415220	10q24.2	10q24.2		617889	"PYROXD2, C10orf33, YUEF"	Pyridine nucleotide-disulphide oxidoreductase domain-containing protein 2	PYROXD2	84795	ENSG00000119943			Pyroxd2 (MGI:1921830)			
chr10	98416192	98446962	10q23.1	10q24.2		604982	HPS1	HPS gene 1	HPS1	3257	ENSG00000107521		"Hermansky-Pudlak syndrome 1, 203300 (3), Autosomal recessive"	Hps1 (MGI:2177763)			
chr10	98457076	99235874	10q23-q24	10q24.2		613469	"HPSE2, HPA2, UFS1"	Heparanase 2	HPSE2	60495	ENSG00000172987		"Urofacial syndrome 1, 236730 (3), Autosomal recessive"	Hpse2 (MGI:2685814)			
chr10	99329098	99394329	10q23-q24	10q24.2		607802	"CNNM1, ACDP1"	Cyclin M1 (ancient conserved domain protein 1)	CNNM1	26507	ENSG00000119946			Cnnm1 (MGI:1891366)			
chr10	99396869	99430772	10q24.1-q25.1	10q24.2		138180	"GOT1, ASTQTL1"	"Glutamic-oxaloacetic transaminase-1, soluble (EC 2.6.1.1)"	GOT1	2805	ENSG00000120053	10q26.1 = conflicting localization	"Aspartate aminotransferase, serum level of, QTL1, 614419 (3)"	Got1 (MGI:95791)			
chr10	99532932	99536523	10q24.2	10q24.2		606727	"NKX2C, NK2.3, CSX3"	"NK2, Drosophila, homolog of, C"	NKX2-3	159296	ENSG00000119919			Nkx2-3 (MGI:97348)			
chr10	99610517	99659506	10q24	10q24.2		609767	"SLC25A28, MRS4L, NPD016"	"Solute carrier family 25 (mitochondrial carrier), member 28"	SLC25A28	81894	ENSG00000155287			Slc25a28 (MGI:2180509)			
chr10	99659376	99711244	10q23-q24	10q24.2		616753	"ENTPD7, LALP1"	Ectonucleoside triphosphate diphosphohydrolase 7	ENTPD7	57089	ENSG00000198018			Entpd7 (MGI:2135885)			
chr10	99694792	99732665	10q24	10q24.2		603646	"COX15, CEMCOX2"	"Cytochrome c oxidase, subunit 15"	COX15	1355	ENSG00000014919		"Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 (3), Autosomal recessive; Leigh syndrome due to cytochrome c oxidase deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Cox15 (MGI:1920112)			
chr10	99732200	99756136	10q24	10q24.2		610101	CUTC	"CutC copper transporter, E. coli, homolog of"	CUTC	51076	ENSG00000119929			Cutc (MGI:1913638)			
chr10	99782597	99853740	10q24	10q24.2		601107	"ABCC2, CMOAT"	"ATP-binding cassette, subfamily C, member 2 (canalicular multispecific organic anion transporter)"	ABCC2	1244	ENSG00000023839		"Dubin-Johnson syndrome, 237500 (3), Autosomal recessive"	Abcc2 (MGI:1352447)			
chr10	99875570	100009952	10q24.2	10q24.2		611282	"DNMBP, TUBA, KIAA1010"	Dynamin-binding protein	DNMBP	23268	ENSG00000107554			Dnmbp (MGI:1917352)			
chr10	100042307	100081884	10q24.2	10q24.2		603103	"CPN1, SCPN, CPN"	"Carboxypeptidase N, polypeptide 1, 50-kD"	CPN1	1369	ENSG00000120054		"Carboxypeptidase N deficiency, 212070 (3), Autosomal recessive"	Cpn1 (MGI:2135874)			
chr10	100150089	100186056	10q24.31	10q24.31		611604	"ERLIN1, SPG62"	Endoplasmic reticulum lipid raft-associated protein 1	ERLIN1	10613	ENSG00000107566		"Spastic paraplegia 62, 615681 (3), Autosomal recessive"	Erlin1 (MGI:2387613)			
chr10	100188297	100229609	10q24	10q24.31		600664	"CHUK, IKBKA, NFKBIKA, IKKA, IKK1"	Conserved helix-loop-helix ubiquitous kinase	CHUK	1147	ENSG00000213341		"Cocoon syndrome, 613630 (3)"	Chuk (MGI:99484)			
chr10	100232295	100267680	10q24.31	10q24.31		616120	"CWF19L1, C19L1, SCAR17"	CWF19-like protein 1	CWF19L1	55280	ENSG00000095485		"Spinocerebellar ataxia, autosomal recessive 17, 616127 (3), Autosomal recessive"	Cwf19l1 (MGI:1919752)			
chr10	100237155	100237301	10q24.31	10q24.31		611330	SNORA12	"Small nucleolar RNA, H/ACA box, 12"	SNORA12	677800		in intron 11 of CWF19L1					
chr10	100273277	100286711	10q24.31	10q24.31		609768	"BLOC1S2, BLOS2"	"Biogenesis of lysosome-related organelles complex 1, subunit 2"	BLOC1S2	282991	ENSG00000196072			Bloc1s2 (MGI:1920939)			
chr10	100288144	100347029	10q24-q25	10q24.31		604532	"PKD2L1, PKDL, PKD2L"	Polycystin L	PKD2L1	9033	ENSG00000107593			Pkd2l1 (MGI:1352448)			
chr10	100347014	100364830	10q24.31	10q24.31		604031	SCD	Stearoyl-CoA desaturase	SCD	6319	ENSG00000099194	pseudogene on chr.17		Scd1 (MGI:98239)			
chr10	100373575	100388353	10q24.31	10q24.31		616240	"OLMALINC, LINC00263, OLMALINCAS"	Oligodendrocyte maturation-associated long intergenic noncoding RNA	OLMALINC	90271		OLMALINCAS is on opposite strand overlapping exon 1 of OLMALINC					
chr10	100463054	100483641	10q24	10q24.31		601396	WNT8B	"Wingless-type MMTV integration site family, member 8B"	WNT8B	7479	ENSG00000075290			Wnt8b (MGI:109485)			
chr10	100486645	100519837	10q24.3	10q24.31		610258	"SEC31B, SEC31L2"	"Sec31, yeast, homolog of, B"	SEC31B	25956	ENSG00000075826			Sec31b (MGI:2685187)			
chr10	100523728	100529922	10q23.2-q23.33	10q24.31		602140	NDUFB8	"NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 2 (8kD, AGGG)"	NDUFB8	4714	ENSG00000166136	previously assigned to 12q21		Ndufb8 (MGI:1914514)			
chr10	100535883	100553923	10q24	10q24.31		606615	"HIF1AN, FIH1"	Hypoxia-inducible factor 1-alpha inhibitor	HIF1AN	55662	ENSG00000166135			Hif1an (MGI:2442345)			
chr10	100735708	100829940	10q24.3-q25.1	10q24.31		167409	"PAX2, PAPRS, FSGS7"	Paired box homeotic gene-2	PAX2	5076	ENSG00000075891		"Glomerulosclerosis, focal segmental, 7, 616002 (3), Autosomal dominant; Papillorenal syndrome, 120330 (3), Autosomal dominant"	Pax2 (MGI:97486)			
chr10	100909415	100965133	10q24	10q24.31		610348	"FAM178A, C10orf6"	"Family with sequence similarity 178, member A"	SLF2	55719	ENSG00000119906			Slf2 (MGI:1924968)			
chr10	100977819	100987518	10q24	10q24.31		611848	MRPL43	Mitochondrial ribosomal protein L43	MRPL43	84545	ENSG00000055950			Mrpl43 (MGI:2137229)			
chr10	100987526	100994402	10q24	10q24.31		606075	"TWNK, C10orf2, TWINKLE, PEOA3, IOSCA, MTDPS7, PRLTS5"	Twinkle mtDNA helicase	TWNK	56652	ENSG00000107815	PEO digenic with POLG	"Mitochondrial DNA depletion syndrome 7 (hepatocerebral type), 271245 (3), Autosomal recessive; Perrault syndrome 5, 616138 (3), Autosomal recessive; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3, 609286 (3), Autosomal dominant"	Twnk (MGI:2137410)			
chr10	100997064	101007835	10q24.3	10q24.31		610454	"LZTS2, KIAA1813, LAPSER1"	"Leucine zipper, putative tumor suppressor 2"	LZTS2	84445	ENSG00000107816			Lzts2 (MGI:2385095)			
chr10	101007682	101031156	10q24.3	10q24.31		612971	PDZD7	PDZ domain-containing 7	PDZD7	79955	ENSG00000186862		"{Retinal disease in Usher syndrome type IIA, modifier of}, 276901 (3), Autosomal recessive; Usher syndrome, type IIC, GPR98/PDZD7 digenic, 605472 (3), Autosomal recessive"	Pdzd7 (MGI:3608325)			
chr10	101031238	101041242	10q24.31	10q24.31		615571	SFXN3	Sideroflexin 3	SFXN3	81855	ENSG00000107819			Sfxn3 (MGI:2137679)			
chr10	101089320	101141265	10q24	10q24.31		612734	TD1	TLX1 divergent gene	TLX1NB	100038246							
chr10	101130772	101137788	10q24	10q24.31		186770	"TLX1, HOX11, TCL3"	"T-cell leukemia, homeobox 1"	TLX1	3195	ENSG00000107807	t(7;10) or t(10;4) in T-ALL		Tlx1 (MGI:98769)			
chr10	101200000	110100000	10q24.32-q25.1			614927	ECTD5	"Ectodermal dysplasia 5, hair/nail type"		101101769		between D10S1239 and D10S1264	"Ectodermal dysplasia 5, hair/nail type, 614927 (2), Autosomal recessive"				
chr10	101226975	101228959	10q24	10q24.32		604255	"LBX1, LBX1H"	"Lady bird late, Drosophila, homolog of, 1"	LBX1	10660	ENSG00000138136			Lbx1 (MGI:104867)			
chr10	101353807	101557320	10q24-q25	10q24.32		603482	"BTRC, BTRCP"	Beta-transducin repeat-containing protein	BTRC	8945	ENSG00000166167			Btrc (MGI:1338871)			
chr10	101578881	101588318	10q23	10q24.32		606343	POLL	"Polymerase, DNA, lambda"	POLL	27343	ENSG00000166169			Poll (MGI:1889000)			
chr10	101588287	101609663	10q24.32	10q24.32		616467	DPCD	"Deleted in primary ciliary dyskinesia, mouse, homolog of"	DPCD	25911	ENSG00000166171			Dpcd (MGI:1924407)			
chr10	101610663	101695294	10q24	10q24.32		608071	"FBXW4, DAC, FBW4, FBWD4"	F-box and WD repeat domain containing 4	FBXW4	6468	ENSG00000107829			Fbxw4 (MGI:1354698)			
chr10	101770129	101780368	10q24	10q24.32		600483	"FGF8, HH6"	Fibroblast growth factor-8	FGF8	2253	ENSG00000107831		"Hypogonadotropic hypogonadism 6 with or without anosmia, 612702 (3), Autosomal dominant"	Fgf8 (MGI:99604)			
chr10	101781324	101783412	10q24-q26	10q24.32		606456	NPM3	"Nucleophosmin/nucleoplasmin family, member 3"	NPM3	10360	ENSG00000107833			Npm3 (MGI:894653)			
chr10	101784442	101818708	10q24.1-q24.3	10q24.32		604039	MGEA5	Meningioma-expressed antigen 5	MGEA5	10724	ENSG00000198408			Mgea5 (MGI:1932139)			
chr10	102065366	102068037	10q24.32	10q24.32		607522	"HPS6, RU"	HPS gene 6	HPS6	79803	ENSG00000166189		"Hermansky-Pudlak syndrome 6, 614075 (3), Autosomal recessive"	Hps6 (MGI:2181763)			
chr10	102102099	102120472	10q24-q25	10q24.32		603451	"LDB1, CLIM2, NLI"	LIM domain-binding factor-1	LDB1	8861	ENSG00000198728			Ldb1 (MGI:894762)			
chr10	102120633	102150332	10q24.2-q24.3	10q24.32		617462	"PPRC1, PRC, KIAA0595"	"Peroxisome proliferator-activated receptor-gamma, coactivator-related protein 1"	PPRC1	23082	ENSG00000148840			Pprc1 (MGI:2385096)			
chr10	102152175	102163870	10q24.32	10q24.32		602394	"NOLC1, p130, NOPP140"	Nucleolar and coiled-body phosphoprotein 1	NOLC1	9221	ENSG00000166197						
chr10	102224766	102229588	10q24.32	10q24.32		611815	"ELOVL3, CIG30"	Elongation of very long chain fatty acids-like 3	ELOVL3	83401	ENSG00000119915			Elovl3 (MGI:1195976)			
chr10	102230188	102241473	10q25	10q24.32		602669	"PITX3, CTPP4, CTRCT11, ASGD1"	Paired-like homeodomain transcription factor-3	PITX3	5309	ENSG00000107859		"Anterior segment dysgenesis 1, multiple subtypes, 107250 (3), Autosomal dominant; Cataract 11, multiple types, 610623 (3), Autosomal dominant; Cataract 11, syndromic, 610623 (3), Autosomal dominant"	Pitx3 (MGI:1100498)			
chr10	102245497	102382898	10q24	10q24.32		603698	GBF1	Golgi-specific brefeldin-A resistance factor 1	GBF1	8729	ENSG00000107862			Gbf1 (MGI:1861607)			
chr10	102394109	102402528	10q24	10q24.32		164012	"NFKB2, LYT10, CVID10"	Nuclear factor of kappa light chain gene enhancer in B-cells 2 (p49/p100); oncogene Lyt-10	NFKB2	4791	ENSG00000077150		"Immunodeficiency, common variable, 10, 615577 (3), Autosomal dominant"	Nfkb2 (MGI:1099800)			
chr10	102402616	102420163	10q24	10q24.32		602327	PSD	Pleckstrin and Sec7 domain protein	PSD	5662	ENSG00000059915			Psd (MGI:1920978)			
chr10	102419221	102423137	10q24.32	10q24.32		610287	"FBXL15, JET"	F-box and leucine-rich repeat protein 15	FBXL15	79176	ENSG00000107872			Fbxl15 (MGI:1915681)			
chr10	102423244	102432665	10q24.32	10q24.32		614142	CUEDC2	Cue domain-containing protein 2	CUEDC2	79004	ENSG00000107874			Cuedc2 (MGI:1914366)			
chr10	102436511	102436583	10q24.32	10q24.32		610567	MIR146B	Micro RNA 146B	MIR146B	574447							
chr10	102479228	102502754	10q24.32	10q24.32		605143	"ACTR1A, ARP1"	Actin-related protein 1A	ACTR1A	10121	ENSG00000138107			Actr1a (MGI:1858964)			
chr10	102502800	102633457	10q24-q25	10q24.32		607035	"SUFU, SUFUXL, SUFUH, JBTS32"	Suppressor of fused	SUFU	51684	ENSG00000107882		"Basal cell nevus syndrome, 109400 (3), Autosomal dominant; Joubert syndrome 32, 617757 (3), Autosomal recessive; Medulloblastoma, desmoplastic, 155255 (3), Autosomal recessive, Autosomal dominant; {Meningioma, familial, susceptibility to}, 607174 (3), Autosomal dominant"	Sufu (MGI:1345643)			
chr10	102644494	102658318	10q24.3	10q24.32		606125	"TRIM8, RNF27, GERP"	Tripartite motif-containing 8	TRIM8	81603	ENSG00000171206			Trim8 (MGI:1933302)			
chr10	102673726	102714432	10q23.3	10q24.32		604695	"ARL3, ARFL3"	ADP-ribosylation factor-like 3	ARL3	403	ENSG00000138175			Arl3 (MGI:1929699)			
chr10	102714517	102739189	10q24.32	10q24.32		615570	SFXN2	Sideroflexin 2	SFXN2	118980	ENSG00000156398			Sfxn2 (MGI:2137678)			
chr10	102742707	102816266	10q24.32	10q24.32		611129	"C10orf26, OPAL1"	Chromosome 10 open reading frame 26	WBP1L	54838	ENSG00000166272			Wbp1l (MGI:107577)			
chr10	102830530	102837532	10q24.3	10q24.32		609300	"CYP17A1, CYP17, P450C17"	"Cytochrome P450, family 17, subfamily A, polypeptide 1 (steroid 17-alpha-hydroxylase)"	CYP17A1	1586	ENSG00000148795	at least 2 genes; distal to GOT1	"17-alpha-hydroxylase/17,20-lyase deficiency, 202110 (3), Autosomal recessive; 17,20-lyase deficiency, isolated, 202110 (3), Autosomal recessive"	Cyp17a1 (MGI:88586)			
chr10	102854209	102864960	10q24.32	10q24.32		616600	"BORCS7, C10orf32"	"BLOC1-related complex, subunit 7"	BORCS7	119032	ENSG00000166275			Borcs7 (MGI:1913689)			
chr10	102869452	102901898	10q24	10q24.32		611806	"AS3MT, CYT19"	Arsenic (+3 oxidation state) methyltransferase	AS3MT	57412	ENSG00000214435			As3mt (MGI:1929882)			
chr10	102918292	103087168	10q24.33	10q24.32		607803	"CNNM2, ACDP2, HOMG6, HOMGSMR"	Cyclin M2	CNNM2	54805	ENSG00000148842		"Hypomagnesemia 6, renal, 613882 (3), Autosomal dominant; Hypomagnesemia, seizures, and mental retardation, 616418 (3), Autosomal recessive, Autosomal dominant"	Cnnm2 (MGI:2151054)			
chr10	103088016	103193305	10q24.3	10q24.32-q24.33		600417	"NT5C2, NT5B, PNT5, SPG45"	"5' nucleotidase, cytosolic II"	NT5C2	22978	ENSG00000076685		"Spastic paraplegia 45, autosomal recessive, 613162 (3), Autosomal recessive"	Nt5c2 (MGI:2178563)			
chr10	103302795	103351133	10q24.33	10q24.33		607816	"PCGF6, RNF134, MBLR"	Polycomb group ring finger 6	PCGF6	84108	ENSG00000156374			Pcgf6 (MGI:1918291)			
chr10	103367952	103389064	10q24-q25.2	10q24.33		601787	"TAF5, TAF2D, TAFII100"	"TAF5 RNA polymerase II, TATA box binding protein-associated factor, 100kD"	TAF5	6877	ENSG00000148835			Taf5 (MGI:2442144)			
chr10	103389049	103396512	10q24	10q24.33		615204	"USMG5, DAPIT"	"Upregulated during skeletal muscle growth 5, mouse, homolog of"	ATP5MD	84833	ENSG00000173915			Usmg5 (MGI:1891435)			
chr10	103396614	103446294	10q24.2-q25.1	10q24.33		612333	"PDCD11, ALG4, NFBP, KIAA0185"	Programmed cell death 11	PDCD11	22984	ENSG00000148843			Pdcd11 (MGI:1341788)			
chr10	103446782	103452404	10q24.33	10q24.33		612235	"CALHM2, FAM26B"	Calcium homeostasis modulator 2	CALHM2	51063	ENSG00000138172			Calhm2 (MGI:1919941)			
chr10	103453386	103458890	10q24.33	10q24.33		612234	"CALHM1, FAM26C"	Calcium homeostasis modulator 1	CALHM1	255022	ENSG00000185933	"?Alzheimer disease, 605526"		Calhm1 (MGI:3643383)			
chr10	103493787	103592551	10q25.1	10q24.33		603804	"NEURL1, NEURL, NEUR1"	Neuralized E3 ubiquitin protein ligase 1	NEURL1	9148	ENSG00000107954			Neurl1a (MGI:1334263)			
chr10	103877557	103918286	10q24.33	10q24.33		613128	"STN1, OBFC1, AAF44"	"STN1, CST complex subunit"	STN1	79991	ENSG00000107960		"Cerebroretinal microangiopathy with calcifications and cysts 2, 617341 (3), Autosomal recessive"	Stn1 (MGI:1915581)			
chr10	103967099	104029232	10q24.33-q25.1	10q24.3-q25.1		616563	"SLK, LOSK, KIAA0204"	STE20-like protein kinase	SLK	9748	ENSG00000065613			Slk (MGI:103241)			
chr10	104000000	133797422	10q25-q26			609750	EIG4	"Epilepsy, idiopathic generalized, susceptibility to 4"		780913		between D16S397 and D16S3095	"{Epilepsy, idiopathic generalized, susceptibility to 4}, 609750 (2)"				
chr10	104000000	117300000	10q25			603266	IDDM17	Insulin-dependent diabetes mellitus-17	IDDM17	8691			"{Diabetes mellitus, insulin-dependent, 17}, 603266 (2)"				
chr10	104031287	104085879	10q24.3	10q25.1		113811	"COL17A1, BPAG2, ERED"	"Collagen XVII, alpha-1 polypeptide"	COL17A1	1308	ENSG00000065618		"Epidermolysis bullosa, junctional, localisata variant, 226650 (3), Autosomal recessive; Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3), Autosomal recessive; Epithelial recurrent erosion dystrophy, 122400 (3), Autosomal dominant"				
chr10	104122057	104126384	10q25.1	10q25.1		616527	"SFR1, MEI5, C10orf78"	SWI5-dependent homologous recombination repair protein 1	SFR1	119392	ENSG00000156384			Sfr1 (MGI:1915038)			
chr10	104129887	104232382	10q25.1	10q25.1		617558	"CFAP43, WDR96, C10orf79, SPGF19"	Cilia- and flagella-associated protein 43	CFAP43	80217	ENSG00000197748		"Spermatogenic failure 19, 617592 (3), Autosomal recessive"	Cfap43 (MGI:1289258)			
chr10	104254193	104267463	10q24-q25	10q25.1		605482	GSTO1	"Glutathione S-transferase, omega-1"	GSTO1	9446	ENSG00000148834			Gsto1 (MGI:1342273)			
chr10	104267625	104304947	10q24-q25	10q25.1		612314	GSTO2	"Glutathione S-transferase, omega-2"	GSTO2	119391	ENSG00000065621			Gsto2 (MGI:1915464)			
chr10	104641100	105265241	10q23.3	10q25.1		606285	"SORCS3, KIAA1059"	SORCS receptor 3	SORCS3	22986	ENSG00000156395			Sorcs3 (MGI:1913923)			
chr10	106573662	107181137	10q23.3	10q25.1		606283	SORCS1	SORCS receptor 1	SORCS1	114815	ENSG00000108018			Sorcs1 (MGI:1929666)			
chr10	109864765	109923552	10q25.3	10q25.1		602443	"XPNPEP1, SAMP, XPNPEPL"	X-prolyl aminopeptidase P1	XPNPEP1	7511	ENSG00000108039			Xpnpep1 (MGI:2180003)			
chr10	109996349	110135564	10q24.2-q24.3	10q25.1-q25.2		601568	"ADD3, ADDL, CPSQ3"	"Adducin-3, gamma"	ADD3	120	ENSG00000148700	fusion with NUP98 in T-ALL	"Cerebral palsy, spastic quadriplegic, 3, 617008 (3), Autosomal recessive"	Add3 (MGI:1351615)			
chr10	110207604	110287364	10q25	10q25.2		600020	MXI1	MAX-interacting protein 1	MXI1	4601	ENSG00000119950		"Neurofibrosarcoma (3); {Prostate cancer, susceptibility to}, 176807 (3), Autosomal dominant"	Mxi1 (MGI:97245)			
chr10	110293039	110304968	10q23	10q25.2		603519	"SMNR, SPF30"	Survival motor neuron-related protein	SMNDC1	10285	ENSG00000119953			Smndc1 (MGI:1923729)			
chr10	110497866	110511543	10q25	10q25.2		603069	"DUSP5, HVH3"	Dual-specificity phosphatase-5	DUSP5	1847	ENSG00000138166			Dusp5 (MGI:2685183)			
chr10	110567690	110604633	10q25	10q25.2		606062	"SMC3, CSPG6, HCAP, BAM, CDLS3"	Structural maintenance of chromosomes 3	SMC3	9126	ENSG00000108055		"Cornelia de Lange syndrome 3, 610759 (3), Autosomal dominant"	Smc3 (MGI:1339795)			
chr10	110641932	110839470	10q25.2	10q25.2		613171	RBM20	RNA-binding motif protein 20	RBM20	282996	ENSG00000203867		"Cardiomyopathy, dilated, 1DD, 613172 (3), Autosomal dominant"	Rbm20 (MGI:1920963)			
chr10	110871794	110900005	10q24	10q25.2		608610	PDCD4	Programmed cell death 4	PDCD4	27250	ENSG00000150593			Pdcd4 (MGI:107490)			
chr10	110898729	110919365	10q25.2	10q25.2		613605	"BBIP1, NCRNA00081, BBIP10, BBS18"	BBSome interacting protein 1	BBIP1	92482	ENSG00000214413	mutation identified in 1 BBS18 family	"?Bardet-Biedl syndrome 18, 615995 (3), Autosomal recessive"	Bbip1 (MGI:1913610)			
chr10	110919369	111013666	10q25	10q25.2		602775	"SHOC2, SIAA0862, SOC2, SUR8"	"Suppressor of clear, C. elegans, homolog of"	SHOC2	8036	ENSG00000108061		"Noonan-like syndrome with loose anagen hair, 607721 (3), Autosomal dominant"	Shoc2 (MGI:1927197)			
chr10	111077031	111080906	10q24-q26	10q25.2		104210	"ADRA2A, ADRA2R"	"Adrenergic, alpha-2A-, receptor"	ADRA2A	150	ENSG00000150594			Adra2a (MGI:87934)			
chr10	112149863	112216305	10q24-q26	10q25.2		602395	GPAM	Glycerol-3-phosphate acyltransferase	GPAM	57678	ENSG00000119927			Gpam (MGI:109162)			
chr10	112283655	112305034	10q25.2	10q25.2		602653	TECTB	"Tectorin, beta"	TECTB	6975	ENSG00000119913			Tectb (MGI:109574)			
chr10	112374157	112428379	10q25.1-q25.2	10q25.2		605677	"ACSL5, FACL5, ACS5"	Acyl-CoA synthetase long-chain family member 5	ACSL5	51703	ENSG00000197142			Acsl5 (MGI:1919129)			
chr10	112446987	112949402	10q25.2	10q25.2		614316	"VTI1A, VTI1RP2, MMDS3"	"VTI1, S. cerevisiae, homolog of, A"	VTI1A	143187	ENSG00000151532			Vti1a (MGI:1855699)			
chr10	112950219	113167677	10q25.3	10q25.2-q25.3		602228	"TCF7L2, TCF4"	Transcription factor 7-like 2	TCF7L2	6934	ENSG00000148737		"{Diabetes mellitus, type 2, susceptibility to}, 125853 (3), Autosomal dominant"	Tcf7l2 (MGI:1202879)			
chr10	113100000	133797422	10q25.3-q26.3			102777	"ADORA2L1, ADORA2L"	Adenosine A2 receptor-like 1									
chr10	113550830	113589601	10q25-q26	10q25.3		603924	"HABP2, PHBP, HGFAL, FSAP, NMTC5"	Hyaluronan-binding protein 2	HABP2	3026	ENSG00000148702	mutation identified in 1 NMTC5 family	"{?Thyroid cancer, nonmedullary, 5}, 616535 (3), Autosomal dominant; {Venous thromboembolism, susceptibility to}, 188050 (3), Autosomal dominant"	Habp2 (MGI:1196378)			
chr10	113588823	113664069	10q24-q26	10q25.3		602873	NRAP	Nebulin-related anchoring protein	NRAP	4892	ENSG00000197893			Nrap (MGI:1098765)			
chr10	113679161	113730908	10q25.1-q25.2	10q25.3		601761	"CASP7, MCH3"	"Caspase 7, apoptosis-related cysteine protease"	CASP7	840	ENSG00000165806			Casp7 (MGI:109383)			
chr10	113834723	113854403	10q25.1	10q25.3		609682	"DCLRE1A, SNM1, SNM1A, KIAA0086"	DNA cross-link repair protein 1A	DCLRE1A	9937	ENSG00000198924			Dclre1a (MGI:1930042)			
chr10	114044046	114046907	10q24-q26	10q25.3		109630	"ADRB1, ADRB1R, RHR"	"Adrenergic, beta-1-, receptor"	ADRB1	153	ENSG00000043591	close linkage to ADRA2R	"{Congestive heart failure and beta-blocker response, modifier of} (3); [Resting heart rate], 607276 (3)"	Adrb1 (MGI:87937)			
chr10	114174441	114232668	10q25.3	10q25.3		605796	TDRD1	Tudor domain protein 1	TDRD1	56165	ENSG00000095627			Tdrd1 (MGI:1933218)			
chr10	114280759	114404777	10q25.3	10q25.3		612420	"AFAP1L2, XB130, KIAA1914"	Actin filament-associated protein 1-like protein 2	AFAP1L2	84632	ENSG00000169129			Afap1l2 (MGI:2147658)			
chr10	114431109	114821642	10q25	10q25.3		602330	LIMAB1	LIM actin-binding protein-1	ABLIM1	3983	ENSG00000099204			Ablim1 (MGI:1194500)			
chr10	114821743	114899826	10q25.3	10q25.3		617312	"FAM160B1, KIAA1600"	"Family with sequence similarity 160, member B1"	FAM160B1	57700	ENSG00000151553			Fam160b1 (MGI:2147545)			
chr10	114938192	114977679	10q25.3	10q25.3		610726	"TRUB1, PUS4"	"TRUB pseudouridine synthase, E. coli, homolog of, 1"	TRUB1	142940	ENSG00000165832			Trub1 (MGI:1919383)			
chr10	115093364	115948998	10q26	10q25.3		612869	"ATRNL1, KIAA0534, ALP"	Attractin-like 1	ATRNL1	26033	ENSG00000107518			Atrnl1 (MGI:2147749)			
chr10	116056924	116273644	10q26	10q25.3		601496	"GFRA1, GDNFRA, GDNFR"	"GDNF family receptor, alpha-1"	GFRA1	2674	ENSG00000151892			Gfra1 (MGI:1100842)			
chr10	116545923	116567857	10q26.1	10q25.3		246600	"PNLIP, PNLIPD"	Pancreatic lipase	PNLIP	5406	ENSG00000175535	mutation identified in 1 family	"?Pancreatic lipase deficiency, 614338 (3), Autosomal recessive"	Pnlip (MGI:97722)			
chr10	116590958	116609174	10q25.3	10q25.3		604422	"PNLIPRP1, PLRP1"	Pancreatic lipase-related protein 1	PNLIPRP1	5407	ENSG00000187021			Pnliprp1 (MGI:97723)			
chr10	116620952	116645142	10q25.3	10q25.3		604423	"PNLIPRP2, PLRP2"	Pancreatic lipase-related protein 2	PNLIPRP2	5408	ENSG00000266200			Pnliprp2 (MGI:1336202)			
chr10	116671191	116853271	10q26.12	10q25.3		610701	"HSPA12A, KIAA0417"	Heat-shock 70kD protein 12A	HSPA12A	259217	ENSG00000165868			Hspa12a (MGI:1920692)			
chr10	116883376	117126585	10q25.3	10q25.3		611171	"KIAA1598, SHOOTIN1"	Kiaa1598 gene	SHTN1	57698	ENSG00000187164			Shtn1 (MGI:1918903)			
chr10	117128520	117138300	10q26.1	10q25.3		604294	"VAX1, MCOPS11"	Ventral anterior homeo box 1	VAX1	11023	ENSG00000148704	mutation identified in one MCOPS11 family	"?Microphthalmia, syndromic 11, 614402 (3), Autosomal recessive"	Vax1 (MGI:1277163)			
chr10	117197488	117210298	10q25.3	10q25.3		613655	"KCNK18, TRESK, TRIK, MGR13"	"Potassium channel, subfamily K, member 18"	KCNK18	338567	ENSG00000186795		"{Migraine, with or without aura, susceptibility to, 13}, 613656 (3)"	Kcnk18 (MGI:2685627)			
chr10	117241072	117279429	10q25	10q25.3		193001	"SLC18A2, VAT2, SVMT"	"Solute carrier family 18 (vesicular monoamine), member 2"	SLC18A2	6571	ENSG00000165646			Slc18a2 (MGI:106677)			
chr10	117280488	117375491	10q25.3-q26.11	10q25.3-q26.1		614235	PDZD8	PDZ domain-containing protein 8	PDZD8	118987	ENSG00000165650			Pdzd8 (MGI:2677270)			
chr10	117300000	133797422	10q26			615163	CORD17	Cone-rod dystrophy 17	CORD17	101409267		between D10S1757 and D10S1782	"Cone-rod dystrophy 17, 615163 (2), Autosomal dominant"				
chr10	117300000	133797422	10q26			609625	"DEL10q26, C10q26DEL"	Chromosome 10q26 deletion syndrome					"Chromosome 10q26 deletion syndrome, 609625 (4), Autosomal dominant"				
chr10	117300000	133797422	10q26			131200	ENDO1	"Endometriosis, susceptibility to, 1"		100188863		max lod at D10S587	"{Endometriosis, susceptibility to, 1}, 131200 (2), Autosomal recessive, Multifactorial"				
chr10	117300000	133797422	10q26			609116	RRIS	Respiratory rhythmicity in sleep		497662			"[Respiratory rhythmicity in sleep], 609116 (2)"				
chr10	117484292	117545067	10q26	10q26.11		607637	EMX2OS	EMX2 opposite strand	EMX2OS	196047		non-coding RNA					
chr10	117542444	117549545	10q26.1	10q26.11		600035	EMX2	"Empty spiracles, Drosophila, homolog of, 2"	EMX2	2018	ENSG00000170370	close to VAX1	"Schizencephaly, 269160 (3)"	Emx2 (MGI:95388)			
chr10	118004915	118046920	10q26	10q26.11		608599	"RAB11FIP2, KIAA0941"	RAB11 family-interacting protein 2	RAB11FIP2	22841	ENSG00000107560			Rab11fip2 (MGI:1922248)			
chr10	118046820	118210152	10q26	10q26.11		608598	CASC2	Cancer susceptibility candidate 2	CASC2	255082		head-to-head orientation with RAB11FIP2					
chr10	118593403	118595647	10q25.3-q26	10q26.11		600895	GPR10	G protein-coupled receptor-10	PRLHR	2834	ENSG00000119973			Prlhr (MGI:2135956)			
chr10	119029715	119033731	10q26.11	10q26.11		608226	"NANOS1, NOS1, SPGF12"	"NANOS, Drosophila, homolog of, 1"	NANOS1	340719	ENSG00000188613		"Spermatogenic failure 12, 615413 (3), Autosomal dominant"	Nanos1 (MGI:2669254)			
chr10	119033669	119080883	10q26	10q26.11		602039	"EIF3A, EIF3S10, P167"	"Eukaryotic translation initiation factor 3, subunit A"	EIF3A	8661	ENSG00000107581			Eif3a (MGI:95301)			
chr10	119140912	119165727	10q26.11	10q26.11		615564	"SFXN4, COXPD18"	Sideroflexin 4	SFXN4	119559	ENSG00000183605		"Combined oxidative phosphorylation deficiency 18, 615578 (3), Autosomal recessive"	Sfxn4 (MGI:2137680)			
chr10	119167698	119178864	10q25-q26	10q26.11		604769	"PRDX3, AOP1"	Peroxiredoxin 3 (antioxidant protein 1)	PRDX3	10935	ENSG00000165672			Prdx3 (MGI:88034)			
chr10	119207684	119455618	10q24-qter	10q26.11		600870	"GRK5, GPRK5"	G protein-coupled receptor kinase 5	GRK5	2869	ENSG00000198873			Grk5 (MGI:109161)			
chr10	119573464	119598840	10q	10q26.11		603413	"TIAL1, TIAR, TCBP"	Tia1 cytotoxic granule-associated RNA-binding protein-like 1	TIAL1	7073	ENSG00000151923			Tial1 (MGI:107913)			
chr10	119651369	119677818	10q25.2-q26.2	10q26.11		603883	"BAG3, MFM6"	BCL2-associated athanogene 3	BAG3	9531	ENSG00000151929		"Cardiomyopathy, dilated, 1HH, 613881 (3), Autosomal dominant; Myopathy, myofibrillar, 6, 612954 (3), Autosomal dominant"	Bag3 (MGI:1352493)			
chr10	119704394	119830481	10q26.11	10q26.11		609389	"INPP5F, SAC2, KIAA0966"	Inositol polyphosphate 5-phosphatase F	INPP5F	22876	ENSG00000198825			Inpp5f (MGI:2141867)			
chr10	119829403	119873627	10q26.11	10q26.11		610909	"MCMBP, C10orf119"	Minichromosome maintenance complex-binding protein	MCMBP	79892	ENSG00000197771			Mcmbp (MGI:1920977)			
chr10	119892572	119944657	10q26.11-q26.12	10q26.11-q26.12		617852	SEC23IP	Sec23-interacting protein	SEC23IP	11196	ENSG00000107651			Sec23ip (MGI:2450915)			
chr10	120851174	120909525	10q26	10q26.12		606417	"WDR11, DR11, KIAA1351, BRWD2, HH14"	WD repeat-containing protein 11	WDR11	55717	ENSG00000120008		"Hypogonadotropic hypogonadism 14 with or without anosmia, 614858 (3), Autosomal dominant"	Wdr11 (MGI:1920230)			
chr10	121478329	121598457	10q26	10q26.13		176943	"FGFR2, BEK, CFD1, JWS, TK14, BBDS"	Fibroblast growth factor receptor-2 (bacteria-expressed kinase)	FGFR2	2263	ENSG00000066468		"Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis, 207410 (3), Autosomal dominant; Apert syndrome, 101200 (3), Autosomal dominant; Beare-Stevenson cutis gyrata syndrome, 123790 (3), Autosomal dominant; Bent bone dysplasia syndrome, 614592 (3), Autosomal dominant; Craniofacial-skeletal-dermatologic dysplasia, 101600 (3), Autosomal dominant; Craniosynostosis, nonspecific (3); Crouzon syndrome, 123500 (3), Autosomal dominant; Gastric cancer, somatic, 613659 (3); Jackson-Weiss syndrome, 123150 (3), Autosomal dominant; LADD syndrome, 149730 (3), Autosomal dominant; Pfeiffer syndrome, 101600 (3), Autosomal dominant; Saethre-Chotzen syndrome, 101400 (3), Autosomal dominant; Scaphocephaly and Axenfeld-Rieger anomaly (3); Scaphocephaly, maxillary retrusion, and mental retardation, 609579 (3)"	Fgfr2 (MGI:95523)			
chr10	121957087	121975227	10q26.13	10q26.13		612987	"NSMCE4A, NSE4A"	"Non-SMC element 4, S. cerevisiae, homolog of, A"	NSMCE4A	54780	ENSG00000107672			Nsmce4a (MGI:1915122)			
chr10	121989173	122254544	10q26	10q26.13		605302	TACC2	"Transforming, acidic, coiled-coil-containing protein 2"	TACC2	10579	ENSG00000138162			Tacc2 (MGI:1928899)			
chr10	122374577	122432354	10q25.3-q26.2	10q26.13		607772	"PLEKHA1, TAPP1"	"Pleckstrin homology domain-containing protein, family A, member 1"	PLEKHA1	59338	ENSG00000107679			Plekha1 (MGI:2442213)			
chr10	122454652	122457351	10q26.13	10q26.13		611313	"LOC387715, ARMD8"	LOC387715 gene	ARMS2	387715	ENSG00000254636		"{Macular degeneration, age-related, 8}, 613778 (3)"				
chr10	122461524	122514907	10q25.3-q26.2	10q26.13		602194	"HTRA1, PRSS11, ARMD7, CARASIL, CADASIL2"	HTRA serine peptidase 1	HTRA1	5654	ENSG00000166033		"CARASIL syndrome, 600142 (3), Autosomal recessive; Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2, 616779 (3), Autosomal dominant; {Macular degeneration, age-related, 7}, 610149 (3); {Macular degeneration, age-related, neovascular type}, 610149 (3)"	Htra1 (MGI:1929076)			
chr10	122560664	122643735	10q25.3-q26.1	10q26.13		601969	DMBT1	Deleted in malignant brain tumors 1	DMBT1	1755	ENSG00000187908			Dmbt1 (MGI:106210)			
chr10	122832154	122846174	10q26.13	10q26.13		616644	"CUZD1, ERG1, ITMAP1"	Cub and zona pellucida-like domains 1	CUZD1	50624	ENSG00000138161			Cuzd1 (MGI:1202881)			
chr10	122980039	122990406	10q26.13	10q26.13		611310	"PSTK, C10orf89"	Phosphoseryl-tRNA kinase	PSTK	118672	ENSG00000179988			Pstk (MGI:2685945)			
chr10	122990805	123008849	10q26.13	10q26.13		606238	"IFZF5, ZNFN1A5, PEGASUS"	Ikaros family zinc finger 5	IKZF5	64376	ENSG00000095574			Ikzf5 (MGI:1914393)			
chr10	123008912	123058289	10q25-q26	10q26.13		600301	"ACADSB, SBCAD"	"Acyl-Coenzyme A dehydrogenase, short/branched chain"	ACADSB	36	ENSG00000196177		"2-methylbutyrylglycinuria, 610006 (3), Autosomal recessive"	Acadsb (MGI:1914135)			
chr10	123136050	123137730	10q26.13	10q26.13		613380	"HMX3, NKX5.1"	H6 family homeobox 3	HMX3	340784	ENSG00000188620			Hmx3 (MGI:107160)			
chr10	123142420	123150672	10q25.2-q26.3	10q26.13		600647	HMX2	Homeo box (H6 family) 2	HMX2	3167	ENSG00000188816			Hmx2 (MGI:107159)			
chr10	123154243	123165369	10q24-q26	10q26.13		603719	BUB3	"Budding uninhibited by benzimidazoles 3, S. cerevisiae, homolog of"	BUB3	9184	ENSG00000154473			Bub3 (MGI:1343463)			
chr10	123666354	123697398	10q26.2-q26.3	10q26.13		604847	GPR26	G protein-coupled receptor 26	GPR26	2849	ENSG00000154478			Gpr26 (MGI:2441758)			
chr10	123745635	123944093	10q26.13	10q26.13		617348	"CPXM2, CPX2"	"Carboxypeptidase X, M14 family, member 2"	CPXM2	119587	ENSG00000121898			Cpxm2 (MGI:1926006)			
chr10	124006058	124093683	10q26	10q26.13		608277	"CHST15, BRAG, KIAA0598"	Carbohydrate sulfotransferase 15	CHST15	51363	ENSG00000182022			Chst15 (MGI:1924840)			
chr10	124397302	124418975	10q26	10q26.13		613349	"OAT, GACR"	Ornithine aminotransferase	OAT	4942	ENSG00000065154	pseudogene at Xp11.2	"Gyrate atrophy of choroid and retina with or without ornithinemia, 258870 (3), Autosomal recessive"	Oat (MGI:97394)			
chr10	124461771	124614140	10q26.13	10q26.13		617231	LHPP	Phospholysine phosphohistidine inorganic pyrophosphate phosphatase	LHPP	64077	ENSG00000107902			Lhpp (MGI:1923679)			
chr10	124619293	124744360	10q26.13	10q26.13		617289	"FAM53B, KIAA0140"	"Family with sequence similarity 53, member B"	FAM53B	9679	ENSG00000189319			Fam53b (MGI:1925188)			
chr10	124757830	124791940	10q26.13	10q26.13		617794	"EEF1AKMT2, METTL10"	EEF1A lysine methyltransferase 2	EEF1AKMT2	399818	ENSG00000203791			Eef1akmt2 (MGI:1919346)			
chr10	124801784	124836669	10q26.13	10q26.13		611144	"FAM175B, ABRO1, KIAA0157"	"Family with sequence similarity 175, member B"	ABRAXAS2	23172	ENSG00000165660			Abraxas2 (MGI:1926116)			
chr10	124939488	124987435	10q26.13	10q26.13		611749	"ZRANB1, TRABID"	Zinc finger- and RAN-binding domain-containing protein 1	ZRANB1	54764	ENSG00000019995			Zranb1 (MGI:106441)			
chr10	124987848	125161060	10q26.13	10q26.13		602619	CTBP2	C-terminal-binding protein 2	CTBP2	1488	ENSG00000175029			Ctbp2 (MGI:1201686)			
chr10	125766452	125775820	10q26.13	10q26.2		608416	"MMP21, HTX7"	Matrix metalloproteinase 21	MMP21	118856	ENSG00000154485		"Heterotaxy, visceral, 7, autosomal, 616749 (3), Autosomal recessive"	Mmp21 (MGI:2664387)			
chr10	125784979	125823279	10q25.2-q26.3	10q26.2		606938	UROS	Uroporphyrinogen III synthase	UROS	7390	ENSG00000188690		"Porphyria, congenital erythropoietic, 263700 (3), Autosomal recessive"	Uros (MGI:98917)			
chr10	125823534	125853694	10q25.3-q26.2	10q26.2		611883	"BCCIP, TOK1"	BRCA2- and CDKN1A-interacting protein	BCCIP	56647	ENSG00000107949			Bccip (MGI:1913415)			
chr10	125836339	125881314	10q26	10q26.2		607960	"DHX32, DDX32"	DEAH (Asp-Glu-Ala-His) box polypeptide 32	DHX32	55760	ENSG00000089876			Dhx32 (MGI:2141813)			
chr10	125896222	126009598	10q26.2	10q26.2		611640	FANK1	Fibronectin type III and ankyrin repeat domains 1	FANK1	92565	ENSG00000203780			Fank1 (MGI:1914180)			
chr10	126012384	126388557	10q26.3	10q26.2		602714	"ADAM12, MLTN"	"A disintegrin and metalloproteinase domain 12 (Meltrin-alpha, mouse, homolog of)"	ADAM12	8038	ENSG00000148848			Adam12 (MGI:105378)			
chr10	126424996	126670509	10q26.2	10q26.2		617735	"C10orf90, FATS"	Chromosome 10 open reading frame 90	C10orf90	118611	ENSG00000154493			D7Ertd443e (MGI:1196431)			
chr10	126905408	127452516	10q26.13-q26.3	10q26.2		601403	"DOCK1, DOCK180"	Dedicator of cytokinesis-1	DOCK1	1793	ENSG00000150760			Dock1 (MGI:2429765)			
chr10	127135425	127196572	10q26.2	10q26.2		617129	"FAM196A, C10orf141, INSYN2"	"Family with sequence similarity 196, member A"	FAM196A	642938	ENSG00000188916			Fam196a (MGI:3605068)			
chr10	127549348	127552670	10q26.2	10q26.2		609513	NPS	Neuropeptide S	NPS	594857	ENSG00000214285			Nps (MGI:3642232)			
chr10	127737273	127741185	10q26.2	10q26.2		617202	FOXI2	Forkhead box I2	FOXI2	399823	ENSG00000186766			Foxi2 (MGI:3028075)			
chr10	127907052	128085854	10q26	10q26.2		600926	PTPRE	"Protein tyrosine phosphatase, receptor type, epsilon"	PTPRE	5791	ENSG00000132334			Ptpre (MGI:97813)			
chr10	128096658	128126404	10q25-qter	10q26.2		176741	MKI67	Proliferation-related Ki-67 antigen	MKI67	4288	ENSG00000148773			Mki67 (MGI:106035)			
chr10	128800000	133797422	10q26.3			166760	OMS	Otitis media susceptibility to		619538		"also 19q, 3p"	"{Otitis media, susceptibility to}, 166760 (2)"				
chr10	129467183	129770982	10q26	10q26.3		156569	MGMT	Methylguanine-DNA methyltransferase	MGMT	4255	ENSG00000170430			Mgmt (MGI:96977)			
chr10	129835231	129964273	10q26.3	10q26.3		607407	"EBF3, COE3, HADDS"	Early B-cell factor 3	EBF3	253738	ENSG00000108001		"Hypotonia, ataxia, and delayed development syndrome, 617330 (3), Autosomal dominant"	Ebf3 (MGI:894289)			
chr10	130136374	130182876	10q26.3	10q26.3		612754	"GLRX3, PICOT"	Glutaredoxin 3	GLRX3	10539	ENSG00000108010			Glrx3 (MGI:1353653)			
chr10	131900643	131971534	10q26.3	10q26.3		613992	PPP2R2D	"Protein phosphatase 2, regulatory subunit B, delta"	PPP2R2D	55844	ENSG00000175470			Ppp2r2d (MGI:1289252)			
chr10	131967682	131982012	10q26.3	10q26.3		603293	"BNIP3, NIP3"	BCL2/adenovirus E1B 19-kD protein-interacting protein 3	BNIP3	664	ENSG00000176171			Bnip3 (MGI:109326)			
chr10	132036067	132184851	10q26.1	10q26.3		611198	"JAKMIP3, C10orf39, NECC2, JAMIP3"	Janus kinase and microtubule interacting protein 3	JAKMIP3	282973	ENSG00000188385			Jakmip3 (MGI:1921254)			
chr10	132184982	132205775	10q25.2-q26	10q26.3		608407	"DPYSL4, CRMP3, ULIP4"	Dihydropyrimidinase-like 4	DPYSL4	10570	ENSG00000151640			Dpysl4 (MGI:1349764)			
chr10	132537778	132783479	10q26.3	10q26.3		600106	INPP5A	"Inositol polyphosphate-5-phosphatase, 40kD"	INPP5A	3632	ENSG00000068383			Inpp5a (MGI:2686961)			
chr10	132782228	132786032	10q26	10q26.3		605955	"NKX6-2, NKX6B, NKX6.2, SPAX8"	"NK6 transcription factor related, locus 2 (Drosophila)"	NKX6-2	84504	ENSG00000148826		"Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy, 617560 (3), Autosomal recessive"	Nkx6-2 (MGI:1352738)			
chr10	133070928	133131674	10q26.3	10q26.3		612302	"ADGRA1, GPR123, KIAA1828"	Adhesion G protein-coupled receptor A1	ADGRA1	84435	ENSG00000197177			Adgra1 (MGI:1277167)			
chr10	133160431	133226411	10q26.3	10q26.3		616237	"KNDC1, RASGEF2, KIAA1768"	Kinase noncatalytic C-lobe domain-containing protein 1	KNDC1	85442	ENSG00000171798			Kndc1 (MGI:1923734)			
chr10	133230273	133231557	10q26	10q26.3		604130	UTF1	Undifferentiated embryonic cell transcription factor 1	UTF1	8433	ENSG00000171794			Utf1 (MGI:1276125)			
chr10	133237903	133241929	10q26.3	10q26.3		607158	"VENTX, VENTX2, HPX42B"	VENT homeobox	VENTX	27287	ENSG00000151650						
chr10	133262415	133276902	10q26.3	10q26.3		602267	"ADAM8, CD156"	A disintegrin and metalloprotease domain 8	ADAM8	101	ENSG00000151651			Adam8 (MGI:107825)			
chr10	133278629	133312336	10q26.3	10q26.3		617817	"TUBGCP2, GCP2, GRIP103, SPC97, ALP4"	Tubulin-gamma complex-associated protein 2	TUBGCP2	10844	ENSG00000130640			Tubgcp2 (MGI:1921487)			
chr10	133325422	133336982	10q26.3	10q26.3		604647	"CALY, DRD1IP"	Calcyon neuron-specific vesicular protein	CALY	50632	ENSG00000130643			Caly (MGI:1915816)			
chr10	133347339	133352682	10q26.3	10q26.3		609776	PRAP1	Proline-rich acidic protein 1	PRAP1	118471	ENSG00000165828			Prap1 (MGI:893573)			
chr10	133352772	133358030	10q26.3	10q26.3		617725	"FUOM, FUCU"	Fucose mutarotase	FUOM	282969	ENSG00000148803			Fuom (MGI:1916314)			
chr10	133362479	133373403	10q26.2-q26.3	10q26.3		602292	"ECHS1, SCEH, ECHS1D"	"Enoyl-CoA hydratase, short-chain, 1, mitochondrial"	ECHS1	1892	ENSG00000127884		"Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3), Autosomal recessive"	Echs1 (MGI:2136460)			
chr10	133379236	133391695	10q26.3	10q26.3		615853	"PAOX, PAO"	Polyamine oxidase	PAOX	196743	ENSG00000148832			Paox (MGI:1916983)			
chr10	133420665	133424616	10q26.3	10q26.3		610447	"SPRN, SHADOO, SHO"	Shadow of prion protein	SPRN	503542	ENSG00000203772			Sprn (MGI:3582583)			
chr10	133527362	133539115	10q24.3-qter	10q26.3		124040	"CYP2E, CYP2E1, P450C2E"	"Cytochrome P450, subfamily IIE, ethanol-inducible"	CYP2E1	1571	ENSG00000130649			Cyp2e1 (MGI:88607)			
chr10	133553899	133568274	10q26.3	10q26.3		611486	"SYCE1, POF12, SPGF15"	Synaptonemal complex central element protein 1	SYCE1	93426	ENSG00000171772	mutation identified in 1 POF12 and 1 SPGF15 family	"?Premature ovarian failure 12, 616947 (3), Autosomal recessive; ?Spermatogenic failure 15, 616950 (3), Autosomal recessive"	Syce1 (MGI:1921325)			
chr11	0	31000000	11p15-p14			606528	"DEL11p15p14, C11DELp15p14"	Chromosome 11p15-p14 deletion syndrome (homozygous)				contiguous gene deletion syndrome	"Chromosome 11p15-p14 deletion syndrome, 606528 (4), Autosomal recessive"				
chr11	0	22000000	11p15			611010	"GINGF4, HGF4, GGF4"	"Fibromatosis, gingival, 4"	GINGF4	100124414		between D11S1984 and D11S1338	"Fibromatosis, gingival, 4, 611010 (2)"				
chr11	0	53400000	11p			604499	HYPLIP2	"Hyperlipidemia, combined, 2"		28515			"Hyperlipidemia, combined, 2, 604499 (2)"				
chr11	0	22000000	11p15			235000	"IH, HHP"	"Hemihyperplasia, isolated"		100188864		epigenetic or uniparental disomy	"Hemihypertrophy, 235000 (2), Autosomal dominant"				
chr11	0	2800000	11p15.5			147510	"IRDN, ILPR"	Insulin-related DNA polymorphism (insulin-related VNTR)									
chr11	0	22000000	11p15			609470	LVNC2	Left ventricular noncompaction 2		619411		max lod at D11S902	"Left ventricular noncompaction 2, 609470 (2)"				
chr11	0	22000000	11p15			616792	NBLST7	"Neuroblastoma, susceptibility to, 7"		107181289		associated with rs2168101	"{Neuroblastoma, susceptibility to, 7}, 616792 (2)"				
chr11	0	53400000	11p			600165	NNO1	Nanophthalmos 1	NNO1	23691			"Nanophthalmos-1, 600165 (2), Autosomal dominant"				
chr11	0	2800000	11p15.5			607967	SLEN3	"Systemic lupus erythematosus with nephritis, susceptibility to, 3"	SLEN3	282849			"{Systemic lupus erythematosus with nephritis, susceptibility to, 3}, 607967 (2)"				
chr11	0	48800000	11pter-p11.2			186710	TP250	T-cell activation antigen p250									
chr11	187880	194574	11p15.5	11p15.5		610176	"SCGB1C1, RYD5"	"Secretoglobin, family 1C, member 1"	SCGB1C1	147199	ENSG00000188076						
chr11	196760	200257	11p15.5	11p15.5		608356	"ODF3, SHIPPO1"	Outer dense fiber of sperm tails 3	ODF3	113746	ENSG00000177947			Odf3 (MGI:1916537)			
chr11	202923	207421	11p15.5	11p15.5		615417	"BET1L, GS15"	BET1-like protein	BET1L	51272	ENSG00000177951			Bet1l (MGI:1913128)			
chr11	207510	215174	11p15.5	11p15.5		609146	RIC8A	"Ric8, C. elegans, homolog of, A"	RIC8A	60626	ENSG00000177963			Ric8a (MGI:2141866)			
chr11	215029	236949	11p15.5	11p15.5		604481	"SIRT3, SIR2L3"	"Sirtuin, S. cerevisiae, homolog 3"	SIRT3	23410	ENSG00000142082			Sirt3 (MGI:1927665)			
chr11	236807	252983	11p15.5	11p15.5		603481	"PSMD13, S11"	"Proteasome 26S subunit, non-ATPase, 13"	PSMD13	5719	ENSG00000185627			Psmd13 (MGI:1345192)			
chr11	278364	285941	11p15.5	11p15.5		609650	"NALP6, PYPAF5"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 6"	NLRP6	171389	ENSG00000174885			Nlrp6 (MGI:2141990)			
chr11	287759	295687	11p15.5	11p15.5		617032	"PGGHG, ATHL1"	Protein-glucosylgalactosylhydroxylysine glucosidase	PGGHG	80162	ENSG00000142102			Pgghg (MGI:2444047)			
chr11	298199	299525	11p15.5	11p15.5		614757	"IFITM5, OI5"	Interferon-induced transmembrane protein 5	IFITM5	387733	ENSG00000206013		"Osteogenesis imperfecta, type V, 610967 (3), Autosomal dominant"	Ifitm5 (MGI:1934923)			
chr11	308106	309409	11p15.5	11p15.5		605578	IFITM2	Interferon-induced transmembrane protein 1	IFITM2	10581	ENSG00000185201			Ifitm2 (MGI:1933382)			
chr11	313990	315271	11p15.5	11p15.5		604456	"IFITM1, IFI17, LEU13"	Interferon-induced transmembrane protein 1	IFITM1	8519							
chr11	319672	320913	11p15.5	11p15.5		605579	IFITM3	Interferon-induced transmembrane protein 3	IFITM3	10410	ENSG00000142089		"{Influenza, severe, susceptibility to}, 614680 (3)"	Ifitm3 (MGI:1913391)			
chr11	392598	404907	11p15	11p15.5		605561	PKP3	Plakophilin-3	PKP3	11187	ENSG00000184363			Pkp3 (MGI:1891830)			
chr11	405715	417453	11p15.5	11p15.5		605478	SIGIRR	Single immunoglobulin domain-containing IL1R-related protein	SIGIRR	59307	ENSG00000185187			Sigirr (MGI:1344402)			
chr11	448214	491399	11p15.5	11p15.5		612793	"PTDSS2, PSS2"	Phosphatidylserine synthase 2	PTDSS2	81490	ENSG00000174915			Ptdss2 (MGI:1351664)			
chr11	494511	507282	11p15.5	11p15.5		173320	"RNH1, RNH"	Ribonuclease/angiogenin inhibitor 1	RNH1	6050	ENSG00000023191			Rnh1 (MGI:1195456)			
chr11	532241	535566	11p15.5	11p15.5		190020	HRAS	Harvey rat sarcoma viral (v-Ha-ras) oncogene homolog	HRAS	3265	ENSG00000174775	pseudogene HRASP on X	"{Bladder cancer, somatic}, 109800 (3); Congenital myopathy with excess of muscle spindles, 218040 (3), Autosomal dominant, Isolated cases; Costello syndrome, 218040 (3), Autosomal dominant, Isolated cases; {Nevus sebaceous or woolly hair nevus, somatic}, 162900 (3); Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200 (3); {Spitz nevus or nevus spilus, somatic}, 137550 (3); {Thyroid carcinoma, follicular, somatic}, 188470 (3)"	Hras (MGI:96224)			
chr11	560970	564024	11p15.5	11p15.5		143023	"RASSF7, C11orf13, HRC1"	"RAS association domain family, member 7"	RASSF7	8045	ENSG00000099849	29kb 5' to HRAS1; divergently transcribed		Rassf7 (MGI:1914235)			
chr11	568088	568197	11p15.5	11p15.5		612982	"MIR210, MIRN210"	Micro RNA 210	MIR210	406992							
chr11	576445	612221	11p15.5	11p15.5		611780	"PHRF1, KIAA1542"	PHD and RING finger domain-containing protein 1	PHRF1	57661	ENSG00000070047			Phrf1 (MGI:2141847)			
chr11	612554	615998	11p15.5	11p15.5		605047	"IRF7, IRF7A, IRF7B, IRF7C, IRF7H, IMD39"	Interferon regulatory factor 7	IRF7	3665	ENSG00000185507	mutation identified in 1 family	"?Immunodeficiency 39, 616345 (3), Autosomal recessive"	Irf7 (MGI:1859212)			
chr11	616564	625066	11p15.5	11p15.5		606839	"CDHR5, MUCDHL"	"Cadherin-related family, member 5"	CDHR5	53841	ENSG00000099834			Cdhr5 (MGI:1919290)			
chr11	626094	627691	11p15.5	11p15.5		182099	SCT	Secretin	SCT	6343	ENSG00000070031						
chr11	637304	640705	11p15.5	11p15.5		126452	DRD4	Dopamine receptor D4	DRD4	1815	ENSG00000069696	proximal to HRAS	"{Attention deficit-hyperactivity disorder}, 143465 (3), Autosomal dominant; Autonomic nervous system dysfunction (3); [Novelty seeking personality], 601696 (1), ?Autosomal dominant"	Drd4 (MGI:94926)			
chr11	644219	695753	11p15.5	11p15.5		602635	"DEAF1, SPN, ZMYND5, MRD24"	"Deaf1, Drosophila, homolog of"	DEAF1	10522	ENSG00000177030	mutation identified in 1 DYSEIDD family	"?Dyskinesia, seizures, and intellectual developmental disorder, 617171 (3), Autosomal recessive; Mental retardation, autosomal dominant 24, 615828 (3), Autosomal dominant"	Deaf1 (MGI:1858496)			
chr11	706119	727726	11p15	11p15.5		614988	"EPS8L2, EPS8R2, DFNB106"	EPS8-like protein 2	EPS8L2	64787	ENSG00000177106		"Deafness autosomal recessive 106, 617637 (3), Autosomal recessive"	Eps8l2 (MGI:2138828)			
chr11	747431	765023	11p15.5-p15.4	11p15.5		602063	TALDO1	Transaldolase-1	TALDO1	6888	ENSG00000177156	pseudogene on chr.1	"Transaldolase deficiency, 606003 (3), Autosomal recessive"	Taldo1 (MGI:1274789)			
chr11	787109	790125	11p15.5	11p15.5		608213	"CEND1, BM88"	Cell cycle exit and neuronal differentiation 1	CEND1	51286	ENSG00000184524			Cend1 (MGI:1929898)			
chr11	790474	798280	11p15.5	11p15.5		609302	"SLC25A22, GC1, EIEE3"	"Solute carrier family 25 (mitochondrial carrier, glutamate), member 22"	SLC25A22	79751	ENSG00000177542		"Epileptic encephalopathy, early infantile, 3, 609304 (3), Autosomal recessive"	Slc25a22 (MGI:1915517)			
chr11	799178	809866	11p15.5	11p15.5		605247	"PIDD1, LRDD"	p53-induced death domain protein 1	PIDD1	55367	ENSG00000177595			Pidd1 (MGI:1889507)			
chr11	809935	812875	11p15.5	11p15.5		180530	RPLP2	"Ribosomal phosphoprotein, large, P2"	RPLP2	6181	ENSG00000177600			Rplp2 (MGI:1914436)			
chr11	818889	825572	11p15.5	11p15.5		609059	"PNPLA2, TTS2, ATGL"	Patatin-like phospholipase domain-containing protein 2	PNPLA2	57104	ENSG00000177666		"Neutral lipid storage disease with myopathy, 610717 (3), Autosomal recessive"	Pnpla2 (MGI:1914103)			
chr11	825557	831990	11p15.5	11p15.5		614177	"EFCAB4A, CRACR2B"	EF-hand calcium-binding domain-containing protein 4A	CRACR2B	283229	ENSG00000177685			Cracr2b (MGI:2446129)			
chr11	832951	838834	11p15.5	11p15.5		602243	"CD151, PETA3, SFA1, MER2"	CD151 antigen	CD151	977	ENSG00000177697		"[Blood group, Raph], 179620 (3); Nephropathy with pretibial epidermolysis bullosa and deafness, 609057 (3)"	Cd151 (MGI:1096360)			
chr11	839720	842528	11p15	11p15.5		601189	"POLR2L, RPB10"	"Polymerase II, RNA, subunit L"	POLR2L	5441	ENSG00000177700			Polr2l (MGI:1913741)			
chr11	842823	867115	11p15.5	11p15.5		602644	"TSPAN4, TM4SF7, NAG2"	Tetraspanin 4	TSPAN4	7106	ENSG00000214063			Tspan4 (MGI:1928097)			
chr11	867858	915057	11p15.5	11p15.5		615692	"CHID1, SICLP"	Chitinase domain-containing protein 1	CHID1	66005	ENSG00000177830			Chid1 (MGI:1915288)			
chr11	925808	1012244	11p15.5	11p15.5		607242	"AP2A2, KIAA0899"	"Adaptor-related protein complex 2, alpha-2 subunit"	AP2A2	161	ENSG00000183020			Ap2a2 (MGI:101920)			
chr11	1012823	1036705	11p15.5-p15.4	11p15.5		158374	MUC6	"Mucin 6, gastric"	MUC6	4588	ENSG00000184956	order: tel-HRAS-MUC6-MUC2-MUC5AC-MUC5B-IGF2-cen		Muc6 (MGI:2663233)			
chr11	1074874	1110507	11p15.5	11p15.5		158370	MUC2	"Mucin 2, intestinal/tracheal"	MUC2	4583	ENSG00000198788			Muc2 (MGI:1339364)			
chr11	1157952	1201137	11p15.5	11p15.5		158373	"MUC5AC, MUC5"	"Mucin 5, subtypes A and C, tracheobronchial/gastric"	MUC5AC	4586	ENSG00000215182			Muc5ac (MGI:104697)			
chr11	1223064	1262175	11p15	11p15.5		600770	MUC5B	"Mucin 5, subtype B, tracheobronchial"	MUC5B	727897	ENSG00000117983		"{Pulmonary fibrosis, idiopathic, susceptibility to}, 178500 (3), Autosomal dominant"	Muc5b (MGI:1921430)			
chr11	1274367	1309661	11p15.5	11p15.5		606277	TOLLIP	Toll-interacting protein	TOLLIP	54472	ENSG00000078902			Tollip (MGI:1891808)			
chr11	1389898	1462688	11p15.5	11p15.5		609236	"BRSK2, SAD1, PEN11B"	BR serine/threonine kinase 2	BRSK2	9024	ENSG00000174672			Brsk2 (MGI:1923020)			
chr11	1469447	1486778	11p15.5	11p15.5		611969	HCCA2	HCCA2 gene	MOB2	81532	ENSG00000182208			Mob2 (MGI:1919891)			
chr11	1554050	1572838	11p15.5	11p15.5		602038	"DUSP8, HVH8"	Dual specificity phosphatase-8	DUSP8	1850	ENSG00000184545	pseudogene on 10q11.2		Dusp8 (MGI:106626)			
chr11	1584341	1585282	11p15.5	11p15.5		148022	"KRTAP5-1, KRN1L"	Keratin associated protein 5-1	KRTAP5-1	387264	ENSG00000205869						
chr11	1752751	1763991	11p15.5	11p15.5		116840	"CTSD, CPSD, CLN10"	Cathepsin D (lysosomal aspartyl protease)	CTSD	1509	ENSG00000117984		"Ceroid lipofuscinosis, neuronal, 10, 610127 (3), Autosomal recessive"	Ctsd (MGI:88562)			
chr11	1827483	1837520	11p15.5	11p15.5		607719	SYT8	Synaptotagmin 8	SYT8	90019	ENSG00000149043			Syt8 (MGI:1859867)			
chr11	1839002	1841679	11p15.5	11p15.5		191043	"TNNI2, AMCD2B, DA2B, FSSV"	"Troponin I, fast-twitch skeletal muscle isoform"	TNNI2	7136	ENSG00000130598		"Arthrogryposis multiplex congenita, distal, type 2B, 601680 (3), Autosomal dominant"	Tnni2 (MGI:105070)			
chr11	1852969	1892262	11p15.5	11p15.5		153432	LSP1	Lymphocyte-specific protein pp52	LSP1	4046	ENSG00000130592			Lsp1 (MGI:96832)			
chr11	1919550	1938705	11p15.5	11p15.5		600692	"TNNT3, AMCD2B, DA2B, FSSV"	"Troponin-T3, skeletal, fast"	TNNT3	7140	ENSG00000130595		"Arthrogryposis, distal, type 2B, 601680 (3), Autosomal dominant"	Tnnt3 (MGI:109550)			
chr11	1947271	2013175	11p15.5	11p15.5		600789	"RPL23L, L23MRP, MRPL23"	Ribosomal protein L23-like (L23 mitochondrial-related protein)	MRPL23	6150	ENSG00000214026			Mrpl23 (MGI:1196612)			
chr11	1995175	2001465	11p15.5	11p15.5		103280	"H19, D11S813E, ASM1, BWS, WT2"	H19 gene	H19	283120		same 200kb fragment as IGF2	"Beckwith-Wiedemann syndrome, 130650 (3), Autosomal dominant; Silver-Russell syndrome, 180860 (3), Isolated cases; Wilms tumor 2, 194071 (3), Autosomal dominant, Somatic mutation"				
chr11	1996758	1996830	11p15.5	11p15.5		615509	MIR675	Micro RNA 675	MIR675	100033819							
chr11	1998744	2003508	11p15.5	11p15.5		616186	ICR1	H19-IGF2-imprinting control region		105259599			"Beckwith-Wiedemann syndrome, 130650 (3), Autosomal dominant"				
chr11	2129111	2149602	11p15.5	11p15.5		147470	"IGF2, GRDF"	"Insulin-like growth factor-2, or somatomedin A"	IGF2	3481	ENSG00000167244	mutation identified in 1 GRDF family	"?Growth restriction, severe, with distinctive facies, 616489 (3), Autosomal dominant"	Igf2 (MGI:96434)			
chr11	2140511	2148665	11p15.5	11p15.5		610146	"IGF2AS, PEG8"	"Insulin-like growth factor II, antisense"	IGF2-AS	51214							
chr11	2159778	2161208	11p15.5	11p15.5		176730	"INS, MODY10, IDDM2"	Insulin	INS	3630	ENSG00000254647	5'--INS-12.6kb-IGF2--3'; cen-HBBC-10cM-INS-2cM-HRAS1-3cM-TH	"Diabetes mellitus, insulin-dependent, 2, 125852 (3), Autosomal dominant; Diabetes mellitus, permanent neonatal, 606176 (3), Autosomal recessive, Autosomal dominant; Hyperproinsulinemia, 616214 (3), Autosomal dominant; Maturity-onset diabetes of the young, type 10, 613370 (3), Autosomal dominant"	Ins2 (MGI:96573)			
chr11	2163928	2174080	11p15.5	11p15.5		191290	"TH, TYH"	Tyrosine hydroxylase	TH	7054	ENSG00000180176	distal to HRAS1	"Segawa syndrome, recessive, 605407 (3), Autosomal recessive"	Th (MGI:98735)			
chr11	2268497	2270951	11p15.5	11p15.5		601886	ASCL2	"Achaete-scute complex, Drosophila, homolog-like 2"	ASCL2	430	ENSG00000183734			Ascl2 (MGI:96920)			
chr11	2295639	2303048	11p15.5	11p15.5		611033	C11orf21	Chromosome 11 open reading frame 21	C11orf21	29125	ENSG00000110665						
chr11	2299479	2318200	11p15.5	11p15.5		603853	"TSPAN32, PHEMX, TSSC6"	Tetraspanin 32	TSPAN32	10077	ENSG00000064201	not imprinted		Tspan32 (MGI:1350360)			
chr11	2376176	2397418	11p	11p15.5		186845	"CD81, TAPA1, CVID6"	CD81 antigen (target of antiproliferative antibody-1)	CD81	975	ENSG00000110651		"Immunodeficiency, common variable, 6, 613496 (3), Autosomal recessive"	Cd81 (MGI:1096398)			
chr11	2398411	2403877	11p15.5	11p15.5		603852	TSSC4	Tumor-suppressing subchromosomal transferable fragment cDNA 4	TSSC4	10078	ENSG00000184281	not imprinted		Tssc4 (MGI:1861712)			
chr11	2403961	2423423	11p15.5	11p15.5		604600	"TRPM5, MTR1"	"Transient receptor potential cation channel, subfamily M, member 5 (MLSN1- and TRP-related gene 1)"	TRPM5	29850	ENSG00000070985	maternal allele imprinted		Trpm5 (MGI:1861718)			
chr11	2444990	2849109	11p15.5	11p15.5-p15.4		607542	"KCNQ1, KCNA9, LQT1, KVLQT1, ATFB3, SQT2"	"Potassium voltage-gated channel, KQT-like subfamily, member 1"	KCNQ1	3784	ENSG00000053918		"Atrial fibrillation, familial, 3, 607554 (3), Autosomal dominant; Jervell and Lange-Nielsen syndrome, 220400 (3), Autosomal recessive; Long QT syndrome 1, 192500 (3), Autosomal dominant; {Long QT syndrome 1, acquired, susceptibility to}, 192500 (3), Autosomal dominant; Short QT syndrome 2, 609621 (3), Autosomal dominant"	Kcnq1 (MGI:108083)			
chr11	2608327	2699997	11p15.5	11p15.5		604115	"KCNQ1OT1, LIT1"	KCNQ1-overlapping transcript 1	KCNQ1OT1	10984			"Beckwith-Wiedemann syndrome, 130650 (3), Autosomal dominant"				
chr11	2800000	11700000	11p15.4			616121	"GVINP1, VLIG1"	"GTPase, very large interferon-inducible, pseudogene 1"	GVINP1	387751							
chr11	2870032	2872104	11p15.5	11p15.4		610980	KCNQ1DN	KCNQ1 downstream neighbor	KCNQ1DN	55539							
chr11	2883217	2885803	11p15.5	11p15.4		600856	"CDKN1C, KIP2, BWS, IMAGE"	"Cyclin-dependent kinase inhibitor 1C (p57, Kip2)"	CDKN1C	1028	ENSG00000129757	rare cause of BWS	"Beckwith-Wiedemann syndrome, 130650 (3), Autosomal dominant; IMAGE syndrome, 614732 (3), Autosomal dominant"				
chr11	2887343	2905503	11p15.5	11p15.4		603240	"SLC22A1LS, ORCTL2S, BWSCR1B"	"Solute carrier family 22, member 1-like-antisense"	SLC22A18AS	5003	ENSG00000254827						
chr11	2899720	2925245	11p15.5	11p15.4		602631	"SLC22A1L, BWSCR1A, IMPT1"	"Solute carrier family 22, member 1-like (Beckwith-Wiedemann region 1A; organic-cation transporter-like 2)"	SLC22A18	5002	ENSG00000110628		"Breast cancer, somatic, 114480 (3); Lung cancer, somatic, 211980 (3); Rhabdomyosarcoma, somatic, 268210 (3)"	Slc22a18 (MGI:1336884)			
chr11	2928272	2929419	11p15.5	11p15.4		602131	"PHLDA2, TSSC3, IPL, BRW1C"	"Pleckstrin homology-like domain, family A, member 2"	PHLDA2	7262	ENSG00000181649			Phlda2 (MGI:1202307)			
chr11	2944429	2992376	11p15.5	11p15.4		601651	"NAP1L4, NAP2L, NAP2"	Nucleosome assembly protein 1-like 4	NAP1L4	4676	ENSG00000205531			Nap1l4 (MGI:1316687)			
chr11	3000921	3057450	11p15.5	11p15.4		123859	CARS	Cysteinyl-tRNA synthetase	CARS	833	ENSG00000110619			Cars (MGI:1351477)			
chr11	3087115	3165351	11p15.4	11p15.4		606733	"OSBPL5, ORP5, KIAA1534"	Oxysterol-binding protein-like protein 5	OSBPL5	114879	ENSG00000021762			Osbpl5 (MGI:1930265)			
chr11	3217943	3218812	11p15.5	11p15.4		607234	"MRGPRG, MRGG"	"MAS-related G protein-coupled receptor family, member G"	MRGPRG	386746	ENSG00000182170			Mrgprg (MGI:3033145)			
chr11	3227652	3232385	11p15.4	11p15.4		607232	"MRGPRE, MRGE"	"Mas-related G protein-coupled receptor family, member E"	MRGPRE	116534	ENSG00000184350			Mrgpre (MGI:2441884)			
chr11	3357926	3379221	11p15.5	11p15.4		602187	ZNF195	Zinc finger protein-195	ZNF195	7748	ENSG00000005801						
chr11	3380960	3409147	11p15.5	11p15.4		608999	TSSC2	Tumor-suppressing subtransferable fragment candidate gene 2	TSSC2	650368							
chr11	3638502	3642391	11p15	11p15.4		610625	ART5	ADP-ribosyltransferase 5	ART5	116969	ENSG00000167311			Art5 (MGI:107948)			
chr11	3645109	3665515	11p15	11p15.4		601625	ART1	ADP-ribosyltransferase 1	ART1	417	ENSG00000129744			Art1 (MGI:107511)			
chr11	3665586	3673628	11p15.5	11p15.4		606372	CHRNA10	"Cholinergic receptor, neuronal nicotinic, alpha polypeptide 10"	CHRNA10	57053	ENSG00000129749			Chrna10 (MGI:3609260)			
chr11	3675009	3797791	11p15	11p15.4		601021	NUP98	"Nucleoporin, 98kD"	NUP98	4928	ENSG00000110713	"fused with HOXA9, NSD1, NSD3, PMX1, HOXC13, DDX10, TOP1, HOXD11 in myeloid leukemia"		Nup98 (MGI:109404)			
chr11	3797723	3826370	11p15.5	11p15.4		615187	"PGAP2, FRAG1, HPMRS3, MRT17, MRT21"	Post-GPI attachment to proteins 2	PGAP2	27315	ENSG00000148985		"Hyperphosphatasia with mental retardation syndrome 3, 614207 (3), Autosomal recessive"				
chr11	3826977	3840982	11p15.5-p15.4	11p15.4		179505	ARHG	"ras homolog gene family, member G (rho G)"	RHOG	391	ENSG00000177105			Rhog (MGI:1928370)			
chr11	3855702	4093209	11p15.5	11p15.4		605921	"STIM1, TAM1, IMD10, STRMK"	Stromal interaction molecule 1	STIM1	6786	ENSG00000167323		"Immunodeficiency 10, 612783 (3), Autosomal recessive; Myopathy, tubular aggregate, 1, 160565 (3), Autosomal dominant; Stormorken syndrome, 185070 (3), Autosomal dominant"	Stim1 (MGI:107476)			
chr11	4094684	4138924	11p15.5	11p15.4		180410	RRM1	"Ribonucleotide reductase, M1 polypeptide"	RRM1	6240	ENSG00000167325			Rrm1 (MGI:98180)			
chr11	4384896	4393695	11p15.5	11p15.4		109092	"TRIM21, SSA1, RO52"	Tripartite motif-containing protein 21	TRIM21	6737	ENSG00000132109			Trim21 (MGI:106657)			
chr11	4598671	4608258	11p15.4	11p15.4		613184	"TRIM68, SS56, GC109"	Tripartite motif-containing protein 68	TRIM68	55128	ENSG00000167333	incorrectly assigned to 2p24 by FISH		Trim68 (MGI:2142077)			
chr11	4643925	4655487	11p15.4	11p15.4		611267	"OR51E1, DGPCR, PSGR2"	"Olfactory receptor, family 51, subfamily E, member 1"	OR51E1	143503	ENSG00000180785			Olfr558 (MGI:3030392)			
chr11	4680170	4697845	11p15.4	11p15.4		611268	"OR51E2, PSGR"	"Olfactory receptor, family 51, subfamily E, member 2"	OR51E2	81285	ENSG00000167332			Olfr78 (MGI:2157548)			
chr11	4988190	4992428	11p15	11p15.4		605470	MMP26	Matrix metalloproteinase 26 (matrilysin 2)	MMP26	56547	ENSG00000167346						
chr11	5225465	5227070	11p15.5	11p15.4		141900	HBB	Hemoglobin beta	HBB	3043	ENSG00000244734	pseudogene HBBP1 between HBG and HBD loci	"Delta-beta thalassemia, 141749 (3), Autosomal dominant; Erythremias, beta- (3); Heinz body anemias, beta-, 140700 (3), Autosomal dominant; Hereditary persistence of fetal hemoglobin, 141749 (3), Autosomal dominant; {Malaria, resistance to}, 611162 (3); Methemoglobinemias, beta- (3); Sickle cell anemia, 603903 (3), Autosomal recessive; Thalassemia-beta, dominant inclusion-body, 603902 (3); Thalassemias, beta-, 613985 (3)"	"Hbb-bt,Hbb-bs (MGI:5474850,MGI:5474852)"			
chr11	5232828	5234627	11p15.5	11p15.4		142000	HBD	Hemoglobin delta	HBD	3045	ENSG00000223609		"Thalassemia due to Hb Lepore (3); Thalassemia, delta- (3)"				
chr11	5244553	5245545	11p15.4	11p15.4		616308	"BGLT3, LINC01083"	"Beta-globin locus transcript 3, noncoding"	BGLT3	103344929							
chr11	5248271	5249856	11p15.5	11p15.4		142200	HBG1	"Hemoglobin, gamma A"	HBG1	3047	ENSG00000213934		"Fetal hemoglobin quantitative trait locus 1, 141749 (3), Autosomal dominant"				
chr11	5253190	5254780	11p15.5	11p15.4		142250	"HBG2, TNCY"	"Hemoglobin, gamma G"	HBG2	3048	ENSG00000196565		"Cyanosis, transient neonatal, 613977 (3), Autosomal dominant; Fetal hemoglobin quantitative trait locus 1, 141749 (3), Autosomal dominant"	Hbb-y (MGI:96027)			
chr11	5268349	5270142	11p15.5	11p15.4		142100	HBE1	Hemoglobin epsilon	HBE1	3046	ENSG00000213931			Hbb-bh1 (MGI:96024)			
chr11	5269924	5304185	11p15.5	11p15.4		152424	LCRB	Locus control region beta		109580095			"Thalassemia, Hispanic gamma-delta-beta, 613985 (3)"				
chr11	5507299	5509984	11p15	11p15.4		605473	UBQLN3	Ubiquilin 3	UBQLN3	50613	ENSG00000175520			Ubqln3 (MGI:3045291)			
chr11	5590905	5685108	11p15	11p15.4		608487	"TRIM5, RNF88"	Tripartite motif-containing protein 5	TRIM5	85363	ENSG00000132256			"Trim5,Trim12c (MGI:4821183,MGI:3646853)"			
chr11	5596100	5612957	11p15	11p15.4		607564	TRIM6	Tripartite motif-containing protein 6	TRIM6	117854	ENSG00000121236			Trim6 (MGI:2137352)			
chr11	5619943	5644397	11p15.4-p15.3	11p15.4		605684	"TRIM34, RNF21, IFP1"	Tripartite motif-containing 34 (RING finger protein-21)	TRIM34	53840	ENSG00000258659						
chr11	5689586	5710862	11p15	11p15.4		606559	"TRIM22, STAF50"	Tripartite motif-containing protein 22	TRIM22	10346	ENSG00000132274						
chr11	6259673	6272126	11p15.5-p15.4	11p15.4		118445	"CCKBR, GASR"	Cholecystokinin B receptor	CCKBR	887	ENSG00000110148			Cckbr (MGI:99479)			
chr11	6390413	6394997	11p15.4-p15.1	11p15.4		607608	"SMPD1, NPD"	"Sphingomyelin phosphodiesterase-1, acid lysosomal"	SMPD1	6609	ENSG00000166311		"Niemann-Pick disease, type A, 257200 (3), Autosomal recessive; Niemann-Pick disease, type B, 607616 (3), Autosomal recessive"	Smpd1 (MGI:98325)			
chr11	6395123	6419829	11p15	11p15.4		602709	"APBB1, FE65"	"Amyloid beta A4 precursor protein-binding, family B, member-1"	APBB1	322	ENSG00000166313			Apbb1 (MGI:107765)			
chr11	6431037	6441023	11p15.5-p15.4	11p15.4		142290	HPX	Hemopexin	HPX	3263	ENSG00000110169			Hpx (MGI:105112)			
chr11	6448612	6474458	11p15.4	11p15.4		605493	"TRIM3, RNF22, BERP"	Tripartite motif-containing 3	TRIM3	10612	ENSG00000110171			Trim3 (MGI:1860040)			
chr11	6474682	6481478	11p15.4	11p15.4		601638	"ARFIP2, POR1"	ADP-ribosylation factor-interacting protein 2	ARFIP2	23647	ENSG00000132254			Arfip2 (MGI:1924182)			
chr11	6481446	6484680	11p15.5-p15.2	11p15.4		607388	"FXC1, TIMM10B"	"Fracture callus 1, rat, homolog of"	TIMM10B	26515	ENSG00000132286			Timm10b (MGI:1315196)			
chr11	6497295	6572024	11p15.4	11p15.4		617277	"DHND1, FLJ00251"	Dynein heavy chain domain 1	DNHD1	144132	ENSG00000179532			Dnhd1 (MGI:1924755)			
chr11	6514829	6603677	11p15.4	11p15.4		615818	"RRP8, NML, KIAA0409"	"Ribosomal RNA processing protein 8, homolog of"	RRP8	23378	ENSG00000132275			Rrp8 (MGI:1914251)			
chr11	6603707	6610873	11p15.5-p15.4	11p15.4		602366	"ILK, P59"	Integrin-linked kinase	ILK	3611	ENSG00000166333			Ilk (MGI:1195267)			
chr11	6610816	6612243	11p15.3	11p15.4		600475	"TAF10, TAF2H, TAF2A"	"TAF10 RNA polymerase II, TATA box-binding protein-associated factor, 30kD"	TAF10	6881	ENSG00000166337			Taf10 (MGI:1346320)			
chr11	6612765	6619460	11p15.5	11p15.4		607998	"TPP1, CLN2, SCAR7"	Tripeptidyl peptidase 1	TPP1	1200	ENSG00000166340		"Ceroid lipofuscinosis, neuronal, 2, 204500 (3), Autosomal recessive; Spinocerebellar ataxia, autosomal recessive 7, 609270 (3), Autosomal recessive"	Tpp1 (MGI:1336194)			
chr11	6621323	6655848	11p15.4	11p15.4		603057	"DCHS1, PCDH16, FIB1, CDH19, VMLDS1, MVP2"	"Dachsous, Drosophila, homolog of, 1"	DCHS1	8642	ENSG00000166341		"Mitral valve prolapse 2, 607829 (3), Autosomal dominant; Van Maldergem syndrome 1, 601390 (3), Autosomal recessive"	Dchs1 (MGI:2685011)			
chr11	6680384	6683400	11p15.5-p15.4	11p15.4		611830	MRPL17	Mitochondrial ribosomal protein L17	MRPL17	63875	ENSG00000158042			Mrpl17 (MGI:1351608)			
chr11	6794524	6795907	11p15	11p15.4		608495	"OR6A2, OR6A1"	"Olfactory receptor, family 6, subfamily A, member 2"	OR6A2	8590	ENSG00000184933			Olfr2 (MGI:97432)			
chr11	6845682	6846635	11p15.4	11p15.4		608493	OR10A1	"Olfactory receptor, family 10, subfamily A, member 1"	OR10A5	144124	ENSG00000166363			Olfr713 (MGI:3030547)			
chr11	6891573	6892499	11p15.4	11p15.4		608494	OR2D2	"Olfactory receptor, family 2, subfamily D, member 2"	OR2D2	120776	ENSG00000166368			"Olfr715,Olfr715b (MGI:3647188,MGI:3030549)"			
chr11	6926360	6991143	11p15.4	11p15.4		605016	ZNF215	Zinc finger protein-215	ZNF215	7762	ENSG00000149054						
chr11	6993481	7020366	11p15.4	11p15.4		605015	ZNF214	Zinc finger protein-214	ZNF214	7761	ENSG00000149050						
chr11	7020445	7089024	11p15.4	11p15.4		609665	"NLRP1, NALP14, NOD5"	"NLR family, pyrin domain containing 1"	NLRP14	338323	ENSG00000158077			Nlrp14 (MGI:1924108)			
chr11	7088933	7091147	11p15	11p15.4		605444	"RBMXL2, HNRNPGT, HNRPGT"	"RNA-binding motif protein, X chromosome, like 2"	RBMXL2	27288	ENSG00000170748			Rbmxl2 (MGI:1923822)			
chr11	7238783	7470031	11p15.4	11p15.4		613528	SYT9	Synaptotagmin 9	SYT9	143425	ENSG00000170743			Syt9 (MGI:1926373)			
chr11	7665094	7678568	11p15.4	11p15.4		608342	CYB5R2	Cytochrome b5 reductase 2	CYB5R2	51700	ENSG00000166394			Cyb5r2 (MGI:2444415)			
chr11	7959020	7965426	11p15	11p15.4		609662	"NLRP10, NALP10, PYNOD, NOD8"	"NLR family, pyrin domain containing 10"	NLRP10	338322	ENSG00000182261			Nlrp10 (MGI:2444084)			
chr11	7987319	7996170	11p15.4	11p15.4		603914	"EIF3F, EIF3S5"	"Eukaryotic translation initiation factor 3, subunit F"	EIF3F	8665	ENSG00000175390			Eif3f (MGI:1913335)			
chr11	8019179	8106106	11p15.4	11p15.4		601197	"TUB, RDOB"	"Tubby, mouse, homolog of"	TUB	7275	ENSG00000166402	mutation identified in 1 RDOB family	"?Retinal dystrophy and obesity, 616188 (3), Autosomal recessive"	Tub (MGI:2651573)			
chr11	8092964	8169093	11p15.4	11p15.4		610509	RIC3	"Resistance to inhibitors of cholinesterase 3, C. elegans, homolog of"	RIC3	79608	ENSG00000166405			Ric3 (MGI:2443887)			
chr11	8224303	8268634	11p15	11p15.4		186921	"LMO1, RBTN1, RHOM1"	LIM domain only 1 (rhombotin 1)	LMO1	4004	ENSG00000166407		"Leukemia, T-cell acute lymphoblastic, 186921 (2)"	Lmo1 (MGI:102812)			
chr11	8335028	8594288	11p15.3	11p15.4		607670	STK33	Serine/threonine protein kinase 33	STK33	65975	ENSG00000130413			Stk33 (MGI:2152419)			
chr11	8612036	8683216	11p15.4	11p15.4		612000	"TRIM66, TIF1D, KIAA0298"	Tripartite motif-containing protein 66	TRIM66	9866	ENSG00000166436			Trim66 (MGI:2152406)			
chr11	8682447	8689871	11p15	11p15.4		603637	RPL27A	Ribosomal protein L27a	RPL27A	6157	ENSG00000166441			Rpl27a (MGI:1347076)			
chr11	8685438	8685568	11p15.4	11p15.4		611333	"SNORA3B, SNORA45"	"Small nucleolar RNA, H/ACA box 3B"	SNORA3B	677826							
chr11	8693351	8910950	11p15	11p15.4		140750	"ST5, HTS1"	Suppression of tumorigenicity-5	ST5	6764	ENSG00000166444			St5 (MGI:108517)			
chr11	8911116	8920078	11p15.3	11p15.4		609191	"AKIP1, BCA3, C11orf17"	Protein kinase A-interacting protein 1	AKIP1	56672	ENSG00000166452			Akip1 (MGI:3041226)			
chr11	8980575	9004650	11p15.3	11p15.4		613125	NRIP3	Nuclear receptor-interacting protein 3	NRIP3	56675	ENSG00000175352			Nrip3 (MGI:1925843)			
chr11	9019499	9091606	11p15.4	11p15.4		611747	SCUBE2	"Signal peptide-, CUB domain-, and EGF-like domains-containing protein 2"	SCUBE2	57758	ENSG00000175356			Scube2 (MGI:1928765)			
chr11	9138824	9265325	11p15.4	11p15.4		617278	"DENND5A, RAB6IP1, KIAA1091, EIEE49"	DENN domain-containing protein 5A	DENND5A	23258	ENSG00000184014		"Epileptic encephalopathy, early infantile, 49, 617281 (3), Autosomal recessive"	Dennd5a (MGI:1201681)			
chr11	9384621	9448126	Chr.11	11p15.4		605586	"IPO7, RANBP7"	Importin 7	IPO7	10527	ENSG00000205339			Ipo7 (MGI:2152414)			
chr11	9460964	9528523	11p15.4-p15.3	11p15.4		603433	"ZNF143, SBF"	Zinc finger protein-143	ZNF143	7702	ENSG00000166478			Zfp143 (MGI:1277969)			
chr11	9573680	9589766	11p15.3-p15.1	11p15.4		193525	WEE1	"wee1+, S. pombe, homolog of"	WEE1	7465	ENSG00000166483			Wee1 (MGI:103075)			
chr11	9664076	9752990	11p15	11p15.4		604762	SWAP70	Switch-associated protein 70	SWAP70	23075	ENSG00000133789			Swap70 (MGI:1298390)			
chr11	9778666	10294206	11p15	11p15.4		607697	"SBF2, MTMR13, CMT4B2"	SET binding factor 2 (myotubularin-related 13)	SBF2	81846	ENSG00000133812		"Charcot-Marie-Tooth disease, type 4B2, 604563 (3), Autosomal recessive"	Sbf2 (MGI:1921831)			
chr11	10304979	10307401	11p15.4	11p15.4		103275	ADM	Adrenomedullin	ADM	133	ENSG00000148926			Adm (MGI:108058)			
chr11	10450320	10507578	11pter-p13	11p15.4		102772	AMPD3	"Adenosine monophosphate deaminase-3, isoform E"	AMPD3	272	ENSG00000133805		"[AMP deaminase deficiency, erythrocytic], 612874 (3), Autosomal recessive"	Ampd3 (MGI:1096344)			
chr11	10511677	10541226	11p15	11p15.4		616641	"RNF141, ZNF230"	RING finger protein 141	RNF141	50862	ENSG00000110315			Rnf141 (MGI:1914400)			
chr11	10557865	10568817	Chr.11	11p15.4		605702	LYVE1	Lymphatic vessel endothelial hyaluronan receptor 1	LYVE1	10894	ENSG00000133800			Lyve1 (MGI:2136348)			
chr11	10573090	10693987	11p15.4-p15.3	11p15.4		604673	"MRVI1, IRAG"	"Murine retrovirus integration site 1, homolog of"	MRVI1	10335	ENSG00000072952			Mrvi1 (MGI:1338023)			
chr11	10750986	10779754	11p15.3	11p15.4		609366	"SH2BP1, KIAA0155, p150"	SH2 domain-binding protein 1	CTR9	9646	ENSG00000198730			Ctr9 (MGI:109345)			
chr11	10797045	10809034	11p15	11p15.4		602325	"EIF4G2, DAP5"	Eukaryotic translation initiation factor 4G-like 1	EIF4G2	1982	ENSG00000110321			Eif4g2 (MGI:109207)			
chr11	10852703	10858072	11p15.3	11p15.4		615251	"ZBED5, BUSTER1"	Zinc finger BED domain-containing protein 5	ZBED5	58486	ENSG00000236287			Zbed5 (MGI:1919220)			
chr11	11270873	11622013	11p15.3	11p15.4		615136	"GALNT18, GALNACT18, GALNTL4"	UPD-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 18	GALNT18	374378	ENSG00000110328			Galnt18 (MGI:2446239)			
chr11	11841422	11959324	11p15.3	11p15.3		614460	USP47	Ubiquitin-specific protease 47	USP47	55031	ENSG00000170242			Usp47 (MGI:1922246)			
chr11	11962995	12009826	11p15.1	11p15.3		605416	"DKK3, RIG"	"Dickkopf, Xenopus, homolog of, 3"	DKK3	27122	ENSG00000050165			Dkk3 (MGI:1354952)			
chr11	12110575	12263789	11p15.3	11p15.3		608881	"MICAL2, KIAA0750"	"Microtubule-associated monooxygenase, calponin and LIM domains-containing 2"	MICAL2	9645	ENSG00000133816			Mical2 (MGI:2444947)			
chr11	12286899	12362139	11p15.3	11p15.3		612355	"MICALCL, EBITEIN1"	MICAL C terminus-like protein	MICALCL	84953	ENSG00000133816			Micalcl (MGI:1918127)			
chr11	12376440	12535355	11p15	11p15.3		608120	PARVA	"Parvin, alpha"	PARVA	55742	ENSG00000197702			Parva (MGI:1931144)			
chr11	12674421	12944736	11p15.2	11p15.3		189967	"TEAD1, TCF13, REF1"	TEA domain family member 1	TEAD1	7003	ENSG00000187079		"Sveinsson chorioretinal atrophy, 108985 (3), Autosomal dominant"	Tead1 (MGI:101876)			
chr11	13009422	13012105	11p15.2	11p15.3		614713	RASSF10	"Ras association domain family, member 10"	RASSF10	644943	ENSG00000189431			Rassf10 (MGI:1925998)			
chr11	13276551	13387267	11p15	11p15.3		602550	"ARNTL, BMAL1, TIC"	Aryl hydrocarbon receptor nuclear translocator-like	ARNTL	406	ENSG00000133794			Arntl (MGI:1096381)			
chr11	13387995	13463296	11p15.2	11p15.3		615933	BTBD10	BTB/POZ domain-containing protein 10	BTBD10	84280	ENSG00000148925			Btbd10 (MGI:1916065)			
chr11	13492044	13496174	11p15.3-p15.1	11p15.3		168450	PTH	Parathyroid hormone	PTH	5741	ENSG00000152266	~9cM distal to CALC1; distal to MYOD	"Hypoparathyroidism, autosomal dominant, 146200 (3), Autosomal dominant; Hypoparathyroidism, autosomal recessive, 146200 (3), Autosomal dominant"	Pth (MGI:97799)			
chr11	13668658	13732345	11p15.2	11p15.3		616107	"FAR1, MLSTD2, PFCRD"	Fatty acyl CoA reductase 1	FAR1	84188	ENSG00000197601		"Peroxisomal fatty acyl-CoA reductase 1 disorder, 616154 (3), Autosomal recessive"	Far1 (MGI:1914670)			
chr11	13962636	14268132	Chr.11	11p15.2		604989	SPON1	"F-spondin, Rat, homolog of"	SPON1	10418	ENSG00000262655			Spon1 (MGI:2385287)			
chr11	14277919	14364505	11pter-p15.5	11p15.2		600098	"RRAS2, TC21"	Related Ras viral oncogene homolog 2	RRAS2	22800	ENSG00000133818		Ovarian carcinoma (3)	Rras2 (MGI:1914172)			
chr11	14457502	14499894	11p15.2	11p15.2		600959	"COPB1, COPB"	"Coatomer protein complex, subunit beta 1"	COPB1	1315	ENSG00000129083			Copb1 (MGI:1917599)			
chr11	14504875	14643633	11p15.1	11p15.2		602854	"PSMA1, PROS30"	"Proteasome subunit, alpha-type, 1"	PSMA1	5682	ENSG00000129084			Psma1 (MGI:1347005)			
chr11	14643690	14874138	11p15	11p15.2		602047	PDE3B	"Phosphodiesterase-3B, cGMP-inhibited"	PDE3B	5140	ENSG00000152270			Pde3b (MGI:1333863)			
chr11	14878004	14898914	11p15.2	11p15.2		608713	CYP2R1	"Cytochrome P450, subfamily IIR, polypeptide 1 (vitamin D 25-hydroxylase)"	CYP2R1	120227	ENSG00000186104		"Rickets due to defect in vitamin D 25-hydroxylation, 600081 (3), Autosomal recessive"	Cyp2r1 (MGI:2449771)			
chr11	14966667	14972360	11p15.2-p15.1	11p15.2		114130	"CALCA, CALC1"	"Calcitonin/calcitonin-related polypeptide, alpha"	CALCA	796	ENSG00000110680	same 220kb fragment as CALCB					
chr11	15073599	15078630	11p15.2-p15.1	11p15.2		114160	"CALCB, CALC2"	"Calcitonin-related polypeptide, beta"	CALCB	797	ENSG00000175868			Calca (MGI:2151253)			
chr11	15111415	15269674	11p15.2	11p15.2		610668	INSC	"Inscuteable, Drosophila, homolog of"	INSC	387755	ENSG00000188487			Insc (MGI:1917942)			
chr11	15966448	16476387	11p15.3-p15.2	11p15.2		607257	SOX6	SRY-box 6	SOX6	55553	ENSG00000110693			Sox6 (MGI:98368)			
chr11	16777296	17014422	11p15.1	11p15.2-p15.1		612686	PLEKHA7	"Pleckstrin homology domain-containing protein, family A, member 7"	PLEKHA7	144100	ENSG00000166689			Plekha7 (MGI:2445094)			
chr11	17074391	17077672	11p	11p15.1		180476	RPS13	Ribosomal protein S13	RPS13	6207	ENSG00000110700			Rps13 (MGI:1915302)			
chr11	17086574	17207995	11p15.1	11p15.1		603601	"PIK3C2A, CPK"	"Phosphatidylinositol 3-kinase, class 2, alpha"	PIK3C2A	5286	ENSG00000011405			Pik3c2a (MGI:1203729)			
chr11	17260336	17349979	11p15-p14	11p15.1		608020	"NUCB2, NEFA"	Nucleobindin 2	NUCB2	4925	ENSG00000070081			Nucb2 (MGI:1858179)			
chr11	17351761	17377320	11p15.1	11p15.1		613714	B7H6	B7 homolog 6	NCR3LG1	374383	ENSG00000188211						
chr11	17385245	17389330	11p15.1	11p15.1		600937	"KCNJ11, BIR, PHHI, HHF2, TNDM3, MODY13"	"Potassium inwardly-rectifying channel, subfamily J, member 11"	KCNJ11	3767	ENSG00000187486	4.5kb 3' of SUR	"Diabetes mellitus, transient neonatal, 3, 610582 (3), Autosomal dominant; {Diabetes mellitus, type 2, susceptibility to}, 125853 (3), Autosomal dominant; Diabetes, permanent neonatal, with or without neurologic features, 606176 (3), Autosomal recessive, Autosomal dominant; Hyperinsulinemic hypoglycemia, familial, 2, 601820 (3), Autosomal recessive; Maturity-onset diabetes of the young, type 13, 616329 (3), Autosomal dominant"	Kcnj11 (MGI:107501)			
chr11	17392884	17476848	11p15.1	11p15.1		600509	"ABCC8, SUR, PHHI, SUR1, HHF1, TNDM2"	"ATP-binding cassette, subfamily C, member 8 (sulfonylurea receptor)"	ABCC8	6833	ENSG00000006071		"Diabetes mellitus, noninsulin-dependent, 125853 (3), Autosomal dominant; Diabetes mellitus, permanent neonatal, 606176 (3), Autosomal recessive, Autosomal dominant; Diabetes mellitus, transient neonatal 2, 610374 (3); Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3), Autosomal recessive, Autosomal dominant; Hypoglycemia of infancy, leucine-sensitive, 240800 (3), Autosomal dominant"	Abcc8 (MGI:1352629)			
chr11	17493894	17544415	11p15.1	11p15.1		605242	"USH1C, DFNB18A"	Harmonin (Usher syndrome 1C gene)	USH1C	10083	ENSG00000006611	Acadian and Samaritan variety	"Deafness, autosomal recessive 18A, 602092 (3), Autosomal recessive; Usher syndrome, type 1C, 276904 (3), Autosomal recessive"	Ush1c (MGI:1919338)			
chr11	17547372	17645943	11p14.3	11p15.1		604487	"OTOG, OTGN, DFNB18B"	Otogelin	OTOG	340990	ENSG00000188162		"Deafness, autosomal recessive 18B, 614945 (3), Autosomal recessive"	Otog (MGI:1202064)			
chr11	17719562	17722130	11p15.4	11p15.1		159970	"MYOD1, MYF3"	Myogenic factor-3	MYOD1	4654	ENSG00000129152	"proximal to CALCA, HBB, BWS, PTH; ?11p14.3"		Myod1 (MGI:97275)			
chr11	17734809	17783054	11p15	11p15.1		176258	"KCNC1, EPM7"	"Potassium voltage-gated channel, Shaw-related subfamily, member 1"	KCNC1	3746	ENSG00000129159		"Epilepsy, progressive myoclonic 7, 616187 (3), Autosomal dominant"	Kcnc1 (MGI:96667)			
chr11	17788047	18013161	11p14	11p15.1		606051	"SERGEF, DELGEF"	Secretion-regulating guanine nucleotide exchange factor	SERGEF	26297	ENSG00000129158			Sergef (MGI:1351630)			
chr11	18020536	18040787	11p15.3-p14	11p15.1		191060	"TPH1, TPH"	Tryptophan hydroxylase 1 (tryptophan-5-monooxygenase)	TPH1	7166	ENSG00000129167			Tph1 (MGI:98796)			
chr11	18120954	18138479	11p15.1	11p15.1		607229	"MRGPRX3, MRGX3"	"Mas-related G protein-coupled receptor family, member X3"	MRGPRX3	117195	ENSG00000179826			"Mrgpra9,Mrgpra1,Mrgpra2b,Mrgpra2a (MGI:3033148,MGI:3033095,MGI:3033098,MGI:3821888)"			
chr11	18172836	18174279	11p15.1	11p15.1		607230	"MRGPRX4, MRGX4"	"Mas-related G protein-coupled receptor family, member X4"	MRGPRX4	117196	ENSG00000179817			Mrgprx1 (MGI:3033139)			
chr11	18231354	18236836	11p15.1	11p15.1		104752	SAA4	"Serum amyloid A4, constitutive"	SAA4	6291	ENSG00000148965						
chr11	18238232	18248673	11p15.1	11p15.1		104751	SAA2	Serum amyloid A2	SAA2	6289	ENSG00000134339	pseudogene = SAA3					
chr11	18266224	18269976	11p15.1	11p15.1		104750	SAA1	Serum amyloid A1	SAA1	6288	ENSG00000173432			"Saa2,Saa1 (MGI:98221,MGI:98222)"			
chr11	18278669	18322497	11p15-p13	11p15.1		607521	"HPS5, RU2, KIAA1017"	"HPS gene 5 (ruby-eye 2, mouse, homolog of)"	HPS5	11234	ENSG00000110756		"Hermansky-Pudlak syndrome 5, 614074 (3), Autosomal recessive"	Hps5 (MGI:2180307)			
chr11	18322268	18367042	11p15.1-p14	11p15.1		189972	GTF2H1	"General transcription factor IIH, polypeptide 1 (62kD subunit)"	GTF2H1	2965	ENSG00000110768	within 50kb of LDHA		Gtf2h1 (MGI:1277216)			
chr11	18394388	18408217	11p15.4	11p15.1		150000	"LDHA, LDH1, GSD11"	Lactate dehydrogenase A	LDHA	3939	ENSG00000134333		"Glycogen storage disease XI, 612933 (3), Autosomal recessive"	Ldha (MGI:96759)			
chr11	18412297	18451245	11p15.5-p15.3	11p15.1		150150	"LDHC, LDH3"	Lactate dehydrogenase C	LDHC	3948	ENSG00000166796	closely linked to LDHB in other species; in man syntenic with LDHA; ?close to LDHA		Ldhc (MGI:96764)			
chr11	18480310	18526955	11p15.2-p15.1	11p15.1		601387	TSG101	Tumor susceptibility gene 101	TSG101	7251	ENSG00000074319		"Breast cancer, somatic, 114480 (3)"	Tsg101 (MGI:106581)			
chr11	18529605	18588837	11p15.2-p15.1	11p15.1		610985	"UEVLD, UEV3, ATTP"	Ubiquitin E2 variant and lactate/malate dehydrogenase domains-containing protein	UEVLD	55293	ENSG00000151116			Uevld (MGI:1860490)			
chr11	18727927	18792720	11p15.2-p15.1	11p15.1		176879	"PTPN5, STEP"	"Protein tyrosine phosphatase, nonreceptor-type, 5 (striatum-enriched)"	PTPN5	84867	ENSG00000110786			Ptpn5 (MGI:97807)			
chr11	18933812	18935001	11p15.1	11p15.1		607227	"MRGPRX1, MRGX1"	"Mas-related G protein-coupled receptor family, member X1"	MRGPRX1	259249	ENSG00000170255			Mrgprb2 (MGI:2441674)			
chr11	19054454	19060680	11p15.1	11p15.1		607228	"MRGPRX2, MRGX2"	"Mas-related G protein-coupled receptor family, member X2"	MRGPRX2	117194	ENSG00000183695			"Mrgprx2,Mrgprb1 (MGI:3033115,MGI:3588270)"			
chr11	19117098	19176419	11p15.1	11p15.1		612815	"ZDHHC13, HIP14L"	Zinc finger DHHC domain-containing protein 13	ZDHHC13	54503	ENSG00000177054			Zdhhc13 (MGI:1919227)			
chr11	19182029	19210570	11p15.1	11p15.1		600824	"CSRP3, CRP3, CLP, CMD1M, CMH12"	Cysteine- and glycine-rich protein 3	CSRP3	8048	ENSG00000129170	mutation identified in 1 CMD1M family	"?Cardiomyopathy, dilated, 1M, 607482 (3); Cardiomyopathy, hypertrophic, 12, 612124 (3), Autosomal dominant"	Csrp3 (MGI:1330824)			
chr11	19224062	19241654	11p15.1	11p15.1		612047	E2F8	E2F transcription factor 8	E2F8	79733	ENSG00000129173			E2f8 (MGI:1922038)			
chr11	19345199	20121600	11p15.1	11p15.1		607026	"NAV2, RAINB1, KIAA1419"	Neuron navigator 2	NAV2	89797	ENSG00000166833			Nav2 (MGI:2183691)			
chr11	20363684	20383782	11p15.1	11p15.1		605628	"HTATIP2, TIP30, CC3"	"HIV-1 TAT-interacting protein 2, 30kD"	HTATIP2	10553	ENSG00000109854			Htatip2 (MGI:1859271)			
chr11	20599399	20655063	11p15.2-p15.1	11p15.1		604159	"SLC6A5, GLYT2, HKPX3"	"Solute carrier family 6 (neurotransmitter transporter, glycine), member 5"	SLC6A5	9152			"Hyperekplexia 3, 614618 (3), Autosomal recessive, Autosomal dominant"	Slc6a5 (MGI:105090)			
chr11	20669550	21575685	11p15.2-p15.1	11p15.1		602319	NELL1	Nel-like 1	NELL1	4745	ENSG00000165973			Nell1 (MGI:2443902)			
chr11	22000000	43400000	11p14.3-p12			185440	ST2	Suppression of tumorigenicity-2	ST2	6761							
chr11	22000000	31000000	11p14			613636	TST1	"Tuberculin skin test reactivity, absence of"		100526790		at chr11:26.37M	"[Tuberculin skin test reactivity, absence of], 613636 (2)"				
chr11	22192484	22283366	11p14.3	11p14.3		608662	"ANO5, TMEM16E, GDD1, LGMD2L"	Anoctamin 5	ANO5	203859	ENSG00000171714		"Gnathodiaphyseal dysplasia, 166260 (3), Autosomal dominant; Miyoshi muscular dystrophy 3, 613319 (3), Autosomal recessive; Muscular dystrophy, limb-girdle, type 2L, 611307 (3), Autosomal recessive"	Ano5 (MGI:3576659)			
chr11	22338120	22379502	11p14.3	11p14.3		607563	"SLC17A6, VGLUT2, DNPI"	"Solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6"	SLC17A6	57084	ENSG00000091664			Slc17a6 (MGI:2156052)			
chr11	22622532	22625840	11p15	11p14.3		613897	FANCF	"Fanconi anemia, complementation group F"	FANCF	2188	ENSG00000183161		"Fanconi anemia, complementation group F, 603467 (3)"	Fancf (MGI:3689889)			
chr11	22627757	22885929	11p15.2-p14.3	11p14.3		602835	GAS2	Growth arrest-specific 2	GAS2	2620	ENSG00000148935			Gas2 (MGI:95657)			
chr11	24496487	25082639	11p14-p13	11p14.3		608178	LUZP2	Leucine zipper protein 2	LUZP2	338645	ENSG00000187398			Luzp2 (MGI:1889615)			
chr11	26189122	26667906	11p14	11p14.3-p14.2		610110	"ANO3, TMEM16C, C11orf25, DYT24"	Anoctamin 3	ANO3	63982	ENSG00000134343		"Dystonia 24, 615034 (3), Autosomal dominant"	Ano3 (MGI:3613666)			
chr11	26200000	63600000	11p14.2-q12.3			612642	DFNA59	"Deafness, autosomal dominant 59"	DFNA59	100271924		between D22S929 and D11S480	"Deafness, autosomal dominant 59, 612642 (2), Autosomal dominant"				
chr11	26667018	26723355	11p14.2	11p14.2		612455	"SLC5A12, SMCT2"	"Solute carrier family 5 (sodium/glucose cotransporter), member 12"	SLC5A12	159963	ENSG00000148942			Slc5a12 (MGI:2138890)			
chr11	26994080	26997086	11p14.2	11p14.2		617085	FIBIN	"Fin bud initiation factor, zebrafish, homolog of"	FIBIN	387758	ENSG00000176971			Fibin (MGI:1914856)			
chr11	27040704	27127806	11p14.2	11p14.2		603312	"BBOX1, BBOX"	"Butyrobetaine-gamma, 2-oxoglutarate dioxygenase 1"	BBOX1	8424	ENSG00000129151			Bbox1 (MGI:1891372)			
chr11	27200000	31000000	11p14.1			612321	"DCDC5, KIAA1493"	Doublecortin domain-containing protein 5									
chr11	27200000	48800000	11p14.1-p11.2			613364	SPG41	Spastic paraplegia 41	SPG41	100359402		max lod 2.36; between D11S1324 and D11S1993	"?Spastic paraplegia 41, autosomal dominant, 613364 (2), Autosomal dominant"				
chr11	27338513	27363247	11p14.1	11p14.1		612324	CCDC34	Coiled-coil domain-containing protein 34	CCDC34	91057	ENSG00000109881			Ccdc34 (MGI:1915451)			
chr11	27365960	27472774	11p14.1	11p14.1		606666	"LGR4, GPR48, BNMD17"	Leucine-rich repeat-containing G protein-coupled receptor 4	LGR4	55366	ENSG00000205213	previously mapped to 5q34-q35.1	"{Bone mineral density, low, susceptibility to}, 615311 (3)"	Lgr4 (MGI:1891468)			
chr11	27494417	27506778	11p14.1	11p14.1		612332	"LIN7C, VELI3, MALS3"	"Lin7, C. elegans, homolog of, C"	LIN7C	55327	ENSG00000148943			Lin7c (MGI:1330839)			
chr11	27506851	27698170	11p14	11p14.1		611468	"BDNFAS, BDNFOS"	BDNF antisense RNA	BDNF-AS	497258							
chr11	27654892	27722057	11p13	11p14.1		113505	"BDNF, BULN2, ANON2"	Brain-derived neurotrophic factor	BDNF	627	ENSG00000176697	homeology with NRF3 on 12p; at p14 boundary	"{Anorexia nervosa, susceptibility to}, 610269 (3); {Bulimia nervosa, age of onset of weight loss in}, 607499 (3), Multifactorial; Central hypoventilation syndrome, congenital, 209880 (3), Autosomal dominant; {Memory impairment, susceptibility to} (3); {Obsessive-compulsive disorder, protection against}, 164230 (3), Autosomal dominant"	Bdnf (MGI:88145)			
chr11	27888170	27891091	11p14.1	11p14.1		140575	"HSP90AA2, HSPCAL3"	"Heat-shock protein, 90kD, alpha, class A, member 2"	HSP90AA2P	3324							
chr11	28020615	28108198	11p14	11p14.1		611271	KIF18A	Kinesin family member 18A	KIF18A	81930	ENSG00000121621			Kif18a (MGI:2446977)			
chr11	28056814	28056909	11p14.1	11p14.1		612330	"MIR610, MIRN610"	Micro RNA 610	MIR610	693195							
chr11	30009740	30017029	11q13.4-q14.1	11p14.1		176266	"KCNA4, KCNA8"	"Potassium voltage-gated channel, shaker-related subfamily, member 4"	KCNA4	3739	ENSG00000182255	other map to 11p		Kcna4 (MGI:96661)			
chr11	30231015	30235276	11p13	11p14.1		136530	"FSHB, HH24"	"Follicle-stimulating hormone, beta polypeptide"	FSHB	2488	ENSG00000131808	distal to AN2	"Hypogonadotropic hypogonadism 24 without anosmia, 229070 (3), Autosomal recessive"	Fshb (MGI:95582)			
chr11	30323098	30338457	11p14.1-p13	11p14.1		612295	C11orf46	Chromosome 11 open reading frame 46	ARL14EP	120534	ENSG00000152219			Arl14ep (MGI:1926020)			
chr11	30384492	30586994	11p14-p13	11p14.1		600911	"MPPED2, C11orf8, D11S302E, 239FB"	Metallophosphoesterase domain-containing protein 2	MPPED2	744	ENSG00000066382			Mpped2 (MGI:1924265)			
chr11	30863602	31369809	11p13	11p14-p13		608062	DCDC1	Doublecortin domain-containing protein 1	DCDC1	341019	ENSG00000170959						
chr11	31000000	63600000	11p13-q12			607644	"CANDF3, CANDN1, FCNC"	"Candidiasis, familial, 3"	CANDN1	338434		between D11S1312 and D11S4191	"Candidiasis, familial, 3, 607644 (2), Autosomal dominant"				
chr11	31000000	36400000	11p13			616902	"DEL11p13, C11DELp13"	"Chromosome 11p13 deletion syndrome, distal"					"Chromosome 11p13 deletion syndrome, distal, 616902 (4), Autosomal dominant"				
chr11	31000000	36400000	11p13			194072	"DEL11p13, C11DELp13, WAGR"	"Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome (chromosome 11p13 deletion syndrome)"				deletion of WT1 and PAX6 genes	"Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, 194072 (4), Autosomal dominant, Somatic mutation"				
chr11	31000000	43400000	11p13-p12			609941	DFNB51	"Deafness, autosomal recessive 51"	DFNB51	448963		max lod at D11S4102	"Deafness, autosomal recessive 51, 609941 (2), Autosomal recessive"				
chr11	31000000	36400000	11p13			117100	"ECT, BECTS"	Centrotemporal epilepsy		100379198		previously assigned to 15q14	"Centrotemporal epilepsy, 117100 (2), Isolated cases"				
chr11	31000000	43400000	11p13-p12			605750	EVR3	Exudative vitreoretinopathy 3	EVR3	81864			"Exudative vitreoretinopathy 3, 605750 (2), Autosomal dominant"				
chr11	31000000	85900000	11p13-q14.1			614344	MRT23	"Mental retardation, autosomal recessive 23"	MRT23	100852398		between rs604518 and rs10899421	"Mental retardation, autosomal recessive 23, 614344 (2), Autosomal recessive"				
chr11	31000000	36400000	11p13			609256	MYP7	Myopia 7	MYP7	553190			"Myopia 7, 609256 (2), Multifactorial"				
chr11	31000000	43400000	11p13-p12			612469	"WAGRO, DEL11p14p12"	"Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome"				contiguous gene deletion syndrome	"WAGRO syndrome, 612469 (4)"				
chr11	31369829	31432834	11p13	11p13		611072	DPH4	"DPH4, S. cerevisiae, homolog of"	DNAJC24	120526	ENSG00000170946			Dnajc24 (MGI:1919522)			
chr11	31432398	31509643	11p13	11p13		612323	"IMMP1L, IMP1"	"Inner mitochondrial membrane peptidase, subunit 1, S. cerevisiae, homolog of"	IMMP1L	196294	ENSG00000148950			Immp1l (MGI:1913791)			
chr11	31509728	31784524	11p13	11p13		606985	"ELP4, PAX6NEB, AN2"	"Elongation protein 4, S. cerevisiae, homolog of"	ELP4	26610	ENSG00000109911	mutation identified in 1 AN2 patient	"?Aniridia 2, 617141 (3), Autosomal dominant"	Elp4 (MGI:1925016)			
chr11	31784791	31817960	11p13	11p13		607108	"PAX6, AN2, MGDA, FVH1, ASGD5"	Paired box homeotic gene-6	PAX6	5080	ENSG00000007372	"mutation identified in 1 patient each with MDGA, COLBN, or COLB"	"Aniridia, 106210 (3), Autosomal dominant; Anterior segment dysgenesis 5, multiple subtypes, 604229 (3); Cataract with late-onset corneal dystrophy, 106210 (3), Autosomal dominant; ?Coloboma of optic nerve, 120430 (3), Autosomal dominant; ?Coloboma, ocular, 120200 (3), Autosomal dominant; Foveal hypoplasia 1, 136520 (3), Autosomal dominant; Keratitis, 148190 (3), Autosomal dominant; ?Morning glory disc anomaly, 120430 (3), Autosomal dominant; Optic nerve hypoplasia, 165550 (3), Autosomal dominant"	Pax6 (MGI:97490)			
chr11	32090930	32105725	11p13	11p13		602735	RCN1	Reticulocalbin 1	RCN1	5954	ENSG00000049449			Rcn1 (MGI:104559)			
chr11	32387774	32435538	11p13	11p13		607102	"WT1, NPHS4"	Wilms tumor-1	WT1	7490	ENSG00000184937	clumped: pter-FSHB-AN2-WT1-CAT	"Denys-Drash syndrome, 194080 (3), Autosomal dominant, Somatic mutation; Frasier syndrome, 136680 (3), Autosomal dominant, Somatic mutation; Meacham syndrome, 608978 (3); Mesothelioma, somatic, 156240 (3); Nephrotic syndrome, type 4, 256370 (3), Autosomal dominant; Wilms tumor, type 1, 194070 (3), Autosomal dominant, Somatic mutation"	Wt1 (MGI:98968)			
chr11	32435517	32458768	11p13	11p13		607899	"WT1AS, WIT1"	WT1 antisense RNA	WT1-AS	51352							
chr11	32583766	32602872	11p13	11p13		609641	"EIF3M, PCID1, B5, GA17"	"Eukaryotic translation initiation factor 3, subunit M"	EIF3M	10480	ENSG00000149100			Eif3m (MGI:1351744)			
chr11	32602079	32794657	11p13	11p13		612328	CCDC73	Coiled-coil domain-containing protein 73	CCDC73	493860	ENSG00000186714			Ccdc73 (MGI:3606488)			
chr11	32829755	32858122	11p13	11p13		611690	"PRRG4, PRGP4, TMG4"	Proline-rich gamma-carboxyglutamic acid protein 4	PRRG4	79056	ENSG00000135378			Prrg4 (MGI:2442211)			
chr11	33015863	33033581	11p13	11p13		612294	"DEPDC7, TR2"	DEP domain-containing protein 7	DEPDC7	91614	ENSG00000121690			Depdc7 (MGI:2139258)			
chr11	33076149	33079453	11p14.1-p13	11p13		612296	LOC283267	LOC283267 gene	LINC00294	283267							
chr11	33084583	33161490	11p13	11p13		600367	CSTF3	"Cleavage stimulation factor, 3' pre-RNA, subunit 3, 77kD"	CSTF3	1479	ENSG00000176102			Cstf3 (MGI:1351825)			
chr11	33256671	33357022	11p13	11p13		604424	"HIPK3, PKY, DYRK6"	Homeodomain-interacting protein kinase-3	HIPK3	10114	ENSG00000110422			Hipk3 (MGI:1314882)			
chr11	33376568	33674101	11p13	11p13		612297	"C11orf41, G2"	Chromosome 11 open reading frame 41	KIAA1549L	25758	ENSG00000110427			D430041D05Rik (MGI:2181743)			
chr11	33703009	33736478	11p13	11p13		107271	"CD59, MIC11"	CD59 antigen (p18-20)	CD59	966	ENSG00000085063	in mouse Ly-6 = multigene complex	"Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy, 612300 (3), Autosomal recessive"	Cd59b (MGI:1888996)			
chr11	33740943	33774524	11p13	11p13		609089	"FBXO3, FBX3, FBA"	F-box only protein 3	FBXO3	26273	ENSG00000110429			Fbxo3 (MGI:1929084)			
chr11	33858575	33892288	11p13	11p13		180385	"LMO2, RBTNL1, RHOM2, TTG2"	LIM domain only 2 (rhombotin-like 1)	LMO2	4005	ENSG00000135363	3rd rhombotin gene not on 11	"Leukemia, acute T-cell, 180385 (2)"	Lmo2 (MGI:102811)			
chr11	34051662	34102609	11p13	11p13		601178	"CAPRIN1, M11S1, GPIAP1, GRIP137"	Cell cycle associated protein 1	CAPRIN1	4076	ENSG00000135387			Caprin1 (MGI:1858234)			
chr11	34105563	34146910	11p13	11p13		609221	"NAT10, ALP, KIAA1709"	N-acetyltransferase 10	NAT10	55226	ENSG00000135372			Nat10 (MGI:2138939)			
chr11	34438924	34472059	11p13	11p13		115500	CAT	Catalase	CAT	847	ENSG00000121691	cen-CAT-WT1-AN2-pter	"Acatalasemia, 614097 (3)"	Cat (MGI:88271)			
chr11	34478790	34513799	11p15-p13	11p13		605169	"ELF5, ESE2"	E74-like factor 5 (epithelium-specific ETS factor 2)	ELF5	2001	ENSG00000135374						
chr11	34621040	34663287	11p12	11p13		605439	"EHF, ESE3"	ETS homologous factor	EHF	26298	ENSG00000135373			Ehf (MGI:1270840)			
chr11	34882294	34916410	11p13	11p13		612491	"APIP, CGI29, MMRP19"	APAF1-interacting protein	APIP	51074	ENSG00000149089			Apip (MGI:1926788)			
chr11	34915828	34996127	11p13	11p13		608769	"PDHX, PDX1, E3BP, PDHXD"	"Pyruvate dehydrogenase complex, lipoyl-containing component X"	PDHX	8050	ENSG00000110435		"Lacticacidemia due to PDX1 deficiency, 245349 (3), Autosomal recessive"	Pdhx (MGI:1351627)			
chr11	35138869	35232401	11pter-p13	11p13		107269	"CD44, MDU2, MDU3, MIC4, IN"	CD44 antigen (homing function)	CD44	960	ENSG00000026508		"[Blood group, Indian system], 609027 (3)"	Cd44 (MGI:88338)			
chr11	35251204	35420062	11p13-p12	11p13		600300	"SLC1A2, EAAT2, EIEE41"	"Solute carrier family 1 (glial high affinity glutamate transporter), member 2"	SLC1A2	6506	ENSG00000110436		"Epileptic encephalopathy, early infantile, 41, 617105 (3), Autosomal dominant"	Slc1a2 (MGI:101931)			
chr11	35618186	35620872	11p13	11p13		612206	FJX1	"Four-jointed box, Drosophila, homolog of, 1"	FJX1	24147	ENSG00000179431			Fjx1 (MGI:1341907)			
chr11	35662691	35811052	11p13	11p13		612298	"TRIM44, AN3"	Tripartite motif-containing protein 44	TRIM44	54765	ENSG00000166326	mutation identified in 1 AN3 family	"?Aniridia 3, 617142 (3), Autosomal dominant"	Trim44 (MGI:1931835)			
chr11	36272291	36289448	11p13	11p13		612299	COMM9	COMM domain-containing protein 9	COMMD9	29099	ENSG00000110442			Commd9 (MGI:1923751)			
chr11	36296174	36465203	11p13-p12	11p13-p12		611728	"PRR5L, PROTOR2, FLJ14213"	Proline-rich protein 5-like	PRR5L	79899	ENSG00000135362			Prr5l (MGI:1919696)			
chr11	36400000	43400000	11p12			611739	BMND8	Bone mineral density QTL 8		100188854		between D11S1392 and D11S4102	"{Osteoporosis}, 166710 (2), Autosomal dominant"				
chr11	36400000	53400000	11p12-p11			610898	PSNP3	"Supranuclear palsy, progressive, 3"		100038248			"Supranuclear palsy, progressive, 3, 610898 (2)"				
chr11	36483766	36510312	11p12	11p12		602355	TRAF6	TNF receptor-associated factor 6	TRAF6	7189	ENSG00000175104			Traf6 (MGI:108072)			
chr11	36510365	36579761	11p13	11p12		179615	RAG1	Recombination activating gene-1	RAG1	5896	ENSG00000166349	assignment to 14 in error	"Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity, 609889 (3); Combined cellular and humoral immune defects with granulomas, 233650 (3), Autosomal recessive; Omenn syndrome, 603554 (3), Autosomal recessive; Severe combined immunodeficiency, B cell-negative, 601457 (3), Autosomal recessive"	Rag1 (MGI:97848)			
chr11	36591942	36598278	11p13	11p12		179616	RAG2	Recombination activating gene-2	RAG2	5897	ENSG00000175097	assignment to 14 in error	"Combined cellular and humoral immune defects with granulomas, 233650 (3), Autosomal recessive; Omenn syndrome, 603554 (3), Autosomal recessive; Severe combined immunodeficiency, B cell-negative, 601457 (3), Autosomal recessive"	Rag2 (MGI:97849)			
chr11	40107065	41460418	11p12	11p12		608817	"LRRC4C, NGL1, KIAA1580"	Leucine rich repeat containing 4C (netrin-G1 ligand)	LRRC4C	57689	ENSG00000148948			Lrrc4c (MGI:2442636)			
chr11	43311954	43344529	11p12	11p12		609774	"API5, AAC11"	Apoptosis inhibitor 5	API5	8539	ENSG00000166181			Api5 (MGI:1888993)			
chr11	43400000	53400000	11p11			609630	CLLS1	"Leukemia, chronic lymphocytic, susceptibility to, 1"		100188791			"{Leukemia, chronic lymphocytic, susceptibility to, 1}, 609630 (2)"				
chr11	43400000	48800000	11p11.2			616229	"OI16, C16DELp11.2, DEL16p11.2"	"Osteogenesis imperfecta, type XVI (chromosome 11p11.2 deletion syndrome, 91.3kb)"					"Osteogenesis imperfecta, type XVI, 616229 (4), Autosomal recessive"				
chr11	43400000	48800000	11p11.2			601224	PSS	Potocki-Shaffer syndrome				contiguous gene syndrome caused by deletion of 11p11.2	"Potocki-Shaffer syndrome, 601224 (4)"				
chr11	43400000	48800000	11p11.2			191270	TYRL	Tyrosinase-like	TYRL	7300							
chr11	43880806	43920274	11p11.12	11p11.2		610603	"ALKBH3, PCA1, DEPC1, ABH3"	"AlkB, E. coli, homolog of, 3"	ALKBH3	221120	ENSG00000166199			Alkbh3 (MGI:1916363)			
chr11	44066117	44084236	11p11	11p11.2		608405	"ACCS, ACS, PHACS"	1-aminocyclopropane-1-carboxylate synthase	ACCS	84680	ENSG00000110455			Accs (MGI:1919717)			
chr11	44095548	44245429	11p12-p11	11p11.2		608210	"EXT2, SSMS"	Exostosin 2	EXT2	2132	ENSG00000151348	mutation identified in 1 SSMS family	"Exostoses, multiple, type 2, 133701 (3), Autosomal dominant; ?Seizures, scoliosis, and macrocephaly syndrome, 616682 (3), Autosomal recessive"	Ext2 (MGI:108050)			
chr11	44260727	44310165	11p11.2	11p11.2		605420	"ALX4, PFM2, FPP, FND2, CRS5"	"Aristaless-like 4, mouse, homolog of"	ALX4	60529	ENSG00000052850		"{Craniosynostosis 5, susceptibility to}, 615529 (3), Autosomal dominant; Frontonasal dysplasia 2, 613451 (3), Autosomal recessive; Parietal foramina 2, 609597 (3), Autosomal dominant"	Alx4 (MGI:108359)			
chr11	44565590	44620362	11p11.2	11p11.2		600623	"CD82, SAR2, KAI1, ST6"	CD82 antigen	CD82	3732	ENSG00000085117		"{Prostate cancer, susceptibility to}, 176807 (2), Autosomal dominant"	Cd82 (MGI:104651)			
chr11	44932347	44951305	11p11.2	11p11.2		617867	"TP53I11, PIG11"	Tumor protein p53-inducible protein 11	TP53I11	9537	ENSG00000175274			Trp53i11 (MGI:2670995)			
chr11	45094012	45235123	11p11.2	11p11.2		616347	"PRDM11, PFM8"	PR domain-containing protein 11	PRDM11	56981	ENSG00000019485			Prdm11 (MGI:2685553)			
chr11	45240301	45286332	Chr.11	11p11.2		607716	"SYT13, KIAA1427"	Synaptotagmin 13	SYT13	57586	ENSG00000019505			Syt13 (MGI:1933945)			
chr11	45647688	45665655	11p11.2-p11.1	11p11.2		603797	"CHST1, KSGAL6ST"	Carbohydrate sulfotransferase-1	CHST1	8534	ENSG00000175264			Chst1 (MGI:1924219)			
chr11	45804071	45813015	11p11.2	11p11.2		605881	"SLC35C1, FUCT1, CDG2C"	"Solute carrier family 35, member C1 (GDP-Fucose transporter 1)"	SLC35C1	55343	ENSG00000181830		"Congenital disorder of glycosylation, type IIc, 266265 (3), Autosomal recessive"	Slc35c1 (MGI:2443301)			
chr11	45847117	45883247	Chr.11	11p11.2		603732	CRY2	Cryptochrome 2	CRY2	1408	ENSG00000121671			Cry2 (MGI:1270859)			
chr11	45885495	45906464	11p12-p11.2	11p11.2		604641	"MAPK8IP1, IB1"	Mitogen-activated protein kinase 8-interacting protein 1	MAPK8IP1	9479	ENSG00000121653		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant"	Mapk8ip1 (MGI:1309464)			
chr11	45909668	45918122	11p12-p11.2	11p11.2		603360	"PEX16, PBD8A, PBD8B"	Peroxisome biogenesis factor 16	PEX16	9409			"Peroxisome biogenesis disorder 8A (Zellweger), 614876 (3), Autosomal recessive; Peroxisome biogenesis disorder 8B, 614877 (3), Autosomal recessive"	Pex16 (MGI:1338829)			
chr11	45921620	45929095	11p11.2	11p11.2		609709	"GYLTL1B, LARGE2"	Glycosyltransferase-like 1B	LARGE2	120071	ENSG00000165905			Large2 (MGI:2443769)			
chr11	45929318	46121433	11p11.2	11p11.2		608325	"PHF21A, BHC80, KIAA1696"	PHD finger protein 21A	PHF21A	51317	ENSG00000135365			Phf21a (MGI:2384756)			
chr11	46277637	46321421	11p11.2	11p11.2		616215	"CREB3L1, OASIS"	cAMP response element-binding protein 3-like 1	CREB3L1	90993	ENSG00000157613			Creb3l1 (MGI:1347062)			
chr11	46332904	46380553	11p11.2	11p11.2		601441	DGKZ	"Diacylglycerol kinase, zeta, 104kD"	DGKZ	8525	ENSG00000149091			Dgkz (MGI:1278339)			
chr11	46380783	46383836	11p11.2	11p11.2		162096	"MDK, NEGF2"	Midkine (neurite growth-promoting factor 2)	MDK	4192	ENSG00000110492			Mdk (MGI:96949)			
chr11	46384791	46386607	11p12-p11.2	11p11.2		118495	CHRM4	"Cholinergic receptor, muscarinic, 4"	CHRM4	1132	ENSG00000180720			Chrm4 (MGI:88399)			
chr11	46396411	46594068	11p11.2	11p11.2		611359	"AMBRA1, KIAA1736"	Activating molecule in beclin 1-regulated autophagy	AMBRA1	55626	ENSG00000110497			Ambra1 (MGI:2443564)			
chr11	46603026	46617893	11p11.2	11p11.2		615086	HARBI1	Harbinger transposase-derived gene 1	HARBI1	283254	ENSG00000180423			Harbi1 (MGI:2443194)			
chr11	46617275	46676018	11p11.2	11p11.2		615088	"ATG13, KIAA0652, PARATARG8"	"Autophagy 13, S. cerevisiae, homolog of"	ATG13	9776	ENSG00000175224			Atg13 (MGI:1196429)			
chr11	46677074	46700664	11p12-q12	11p11.2		602732	"ARHGAP1, RHOGAP1, CDC42GAP"	RHO GTPase-activating protein 1	ARHGAP1	392	ENSG00000175220			Arhgap1 (MGI:2445003)			
chr11	46700766	46705915	11p11.2	11p11.2		616454	"ZNF408, EVR6, RP72"	Zinc finger protein 408	ZNF408	79797	ENSG00000175213	mutation identified in 1 EVR6 family	"?Exudative vitreoretinopathy 6, 616468 (3), Autosomal dominant; Retinitis pigmentosa 72, 616469 (3), Autosomal recessive"	Zfp408 (MGI:2685857)			
chr11	46719165	46739507	11p11-q12	11p11.2		176930	"F2, THPH1, RPRGL2"	Coagulation factor II (thrombin)	F2	2147	ENSG00000180210		"Dysprothrombinemia, 613679 (3), Autosomal recessive; Hypoprothrombinemia, 613679 (3), Autosomal recessive; {Pregnancy loss, recurrent, susceptibility to, 2}, 614390 (3), Autosomal dominant; {Stroke, ischemic, susceptibility to}, 601367 (3), Multifactorial; Thrombophilia due to thrombin defect, 188050 (3), Autosomal dominant"	F2 (MGI:88380)			
chr11	46743533	46846307	11p11.2	11p11.2		611142	"CKAP5, CHTOG, MSPS, KIAA0097"	Cytoskeleton-associated protein 5	CKAP5	9793	ENSG00000175216			Ckap5 (MGI:1923036)			
chr11	46854714	46918621	11p12-p11.2	11p11.2		604270	"LRP4, MEGF7, CLSS, SOST2, CMS17"	Low density lipoprotein receptor-related protein 4	LRP4	4038	ENSG00000134569	mutation identified in 1 CMS17 family	"Cenani-Lenz syndactyly syndrome, 212780 (3), Autosomal recessive; ?Myasthenic syndrome, congenital, 17, 616304 (3), Autosomal recessive; Sclerosteosis 2, 614305 (3), Autosomal recessive, Autosomal dominant"	Lrp4 (MGI:2442252)			
chr11	47164297	47177124	11p11.2-p11.12	11p11.2		606908	"ARFGAP2, ZNF289"	ADP-ribosylation factor GTPase-activating protein 2	ARFGAP2	84364	ENSG00000149182			Arfgap2 (MGI:1924288)			
chr11	47177520	47186458	11p11	11p11.2		606513	PACSIN3	Protein kinase C and casein kinase substrate in neurons 3	PACSIN3	29763	ENSG00000165912			Pacsin3 (MGI:1891410)			
chr11	47214941	47239217	11p12-p11	11p11.2		600811	DDB2	"Damage-specific DNA binding protein 2, 48kD"	DDB2	1643	ENSG00000134574		"Xeroderma pigmentosum, group E, DDB-negative subtype, 278740 (3), Autosomal recessive"	Ddb2 (MGI:1355314)			
chr11	47239301	47248846	11p11.2	11p11.2		171650	ACP2	"Acid phosphatase 2, lysosomal"	ACP2	53	ENSG00000134575		"?Lysosomal acid phosphatase deficiency, 200950 (1), Autosomal recessive"	Acp2 (MGI:87882)			
chr11	47248299	47269032	11p11.2	11p11.2		602423	"NR1H3, LXRA"	"Nuclear receptor subfamily 1, group H, member 3"	NR1H3	10062	ENSG00000025434			Nr1h3 (MGI:1352462)			
chr11	47269375	47330030	11p11.2	11p11.2		603584	"MADD, DENN"	MAP kinase-activating death domain (differentially expressed in normal and neoplastic cells)	MADD	8567	ENSG00000110514			Madd (MGI:2444672)			
chr11	47331405	47352701	11p11.2	11p11.2		600958	"MYBPC3, CMH4, CMD1MM, LVNC10"	"Myosin-binding protein C, cardiac"	MYBPC3	4607	ENSG00000134571		"Cardiomyopathy, dilated, 1MM, 615396 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 4, 115197 (3), Autosomal dominant; Left ventricular noncompaction 10, 615396 (3), Autosomal dominant"	Mybpc3 (MGI:102844)			
chr11	47354857	47395639	11p11.2	11p11.2		165170	"SPI1, SFPI1"	Oncogene SPI1	SPI1	6688	ENSG00000066336			Spi1 (MGI:98282)			
chr11	47407131	47416500	11p11.2	11p11.2		608735	"SLC39A13, ZIP13, EDSSPD3"	"Solute carrier family 39 (zinc transporter), member 13"	SLC39A13	91252	ENSG00000165915		"Ehlers-Danlos syndrome, spondylodysplastic type, 3, 612350 (3), Autosomal recessive"	Slc39a13 (MGI:1915677)			
chr11	47418768	47426472	11p13-p12	11p11.2		186852	"PSMC3, TBP1"	"Proteasome (prosome, macropain) 26S subunit, ATPase, 3"	PSMC3	5702	ENSG00000165916			Psmc3 (MGI:1098754)			
chr11	47437756	47449177	11p11.2-p11.1	11p11.2		601592	"RAPSN, CMS1D, CMS11, FADS"	"Receptor-associated protein of the synapse, 43kD"	RAPSN	5913	ENSG00000165917		"Fetal akinesia deformation sequence, 208150 (3), Autosomal recessive; Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency, 616326 (3), Autosomal recessive"	Rapsn (MGI:99422)			
chr11	47465932	47565568	11p11	11p11.2		601074	"CELF1, CUGBP1, NAB50, BRUNOL2, CUGBP"	"CUGbp and ELAV-like family, member 1"	CELF1	10658	ENSG00000149187						
chr11	47572196	47579014	11p11.2	11p11.2		617645	"KBTBD4, HSPC252, BKLHD4"	KELCH repeat- and BTB/POZ domain-containing protein 4	KBTBD4	55709	ENSG00000123444			Kbtbd4 (MGI:1914386)			
chr11	47579009	47584562	11p11.11	11p11.2		603846	NDUFS3	"NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kD"	NDUFS3	4722	ENSG00000213619		"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufs3 (MGI:1915599)			
chr11	47589663	47596335	11p11.2	11p11.2		614911	"C1QTNF4, CTRP4"	C1q- and tumor necrosis factor-related protein 4	C1QTNF4	114900	ENSG00000172247			C1qtnf4 (MGI:1914695)			
chr11	47604308	47642653	11q12.1	11p11.2		613221	MTCH2	Mitochondrial carrier homolog 2	MTCH2	23788	ENSG00000109919			Mtch2 (MGI:1929260)			
chr11	47659167	47715381	11p11.2	11p11.2		617345	"AGBL2, CCP2"	ATP/GTP-binding protein-like 2	AGBL2	79841	ENSG00000165923			Agbl2 (MGI:2443254)			
chr11	47716493	47767477	11p11.2	11p11.2		615265	"FNBP4, FBP30, KIAA1014"	Formin-binding protein 4	FNBP4	23360	ENSG00000109920			Fnbp4 (MGI:1860513)			
chr11	47778082	47848543	11p11.2	11p11.2		607614	"NUP160, KIAA0197"	"Nucleoporin, 160kD"	NUP160	23279	ENSG00000030066			Nup160 (MGI:1926227)			
chr11	47980503	48170841	11p11.2	11p11.2		600925	"PTPRJ, DEP1"	"Protein tyrosine phosphatase, receptor type, J polypeptide"	PTPRJ	5795	ENSG00000149177		"Colon cancer, somatic, 114500 (3)"	Ptprj (MGI:104574)			
chr11	49145093	49208669	11p11.2	11p11.12		600934	"FOLH1, FOLH, PSM, PSMA"	Folate hydrolase 1 (prostate-specific membrane antigen)	FOLH1	2346	ENSG00000086205	?pseudogene on 11q14					
chr11	54603068	54603997	11p11.12	11q11		614273	OR4C46	"Olfactory receptor, family 4, subfamily C, member 46"	OR4C46	119749	ENSG00000185926			Olfr1258 (MGI:3031092)			
chr11	55800000	77400000	11q12.1-q13.5			135610	FNL2	Fibronectin-like-2									
chr11	55800000	66100000	11q12-q13.1			612795	PURAQTL1	Polyunsaturated fatty acids plasma level QTL1		100302559		associated with rs174537	"[Polyunsaturated fatty acids plasma level QTL1], 612795 (2)"				
chr11	55800000	63600000	11q12			608687	"SCA20, DUP11q12, C11DUPq12"	"Spinocerebellar ataxia 20 (chromosome 11q12 duplication syndrome, 260kb)"				contiguous gene duplication syndrome	"Spinocerebellar ataxia 20, 608687 (4), Autosomal dominant"				
chr11	55935455	55936399	11q12.1	11q12.1		608496	"OR5I1, OLF1"	"Olfactory receptor, family 5, subfamily I, member 1"	OR5I1	10798	ENSG00000167825			Olfr152 (MGI:1313139)			
chr11	55993680	55994624	11q12.1	11q12.1		608492	OR5F1	"Olfactory receptor, family 5, subfamily F, member 1"	OR5F1	338674	ENSG00000149133						
chr11	57181746	57191713	11q12.1	11q12.1		615213	LRRC55	Leucine-rich repeat-containing protein 55	LRRC55	219527	ENSG00000183908			Lrrc55 (MGI:2685197)			
chr11	57233576	57237452	11q12	11q12.1		600052	"APLNR, AGTRL1, APJ"	Apelin receptor	APLNR	187	ENSG00000134817			Aplnr (MGI:1346086)			
chr11	57299628	57324951	11q12	11q12.1		607104	"TNKS1BP1, TAB182, KIAA1741"	"Tankyrase 1-binding protein 1, 182kD"	TNKS1BP1	85456	ENSG00000149115			Tnks1bp1 (MGI:2446193)			
chr11	57325984	57335876	11q12	11q12.1		604328	"SSRP1, FACT"	Structure-specific recognition protein 1	SSRP1	6749	ENSG00000149136			Ssrp1 (MGI:107912)			
chr11	57335942	57372398	11q12	11q12.1		600843	"P2RX3, P2X3"	"Purinergic receptor P2X, ligand-gated ion channel, 3"	P2RX3	5024	ENSG00000109991			P2rx3 (MGI:1097160)			
chr11	57376768	57381149	11cen-q12	11q12.1		606814	"PRG3, MBPH"	Proteoglycan 3	PRG3	10394	ENSG00000156575			Prg3 (MGI:1858200)			
chr11	57386786	57390656	11cen-q12	11q12.1		605601	"PRG2, MBP"	Proteoglycan 2	PRG2	5553	ENSG00000186652			Prg2 (MGI:103294)			
chr11	57460536	57477538	11q12.1	11q12.1		610462	"RTN4RL2, NGRH1, NGR2"	Reticulon 4 receptor-like 2	RTN4RL2	349667	ENSG00000186907			Rtn4rl2 (MGI:2669796)			
chr11	57484530	57516560	11p11.2-p11.1	11q12.1		603733	"SLC43A1, LAT3, POV1"	"Solute carrier family 43 (L-type amino acid transporter), member 1"	SLC43A1	8501	ENSG00000149150			Slc43a1 (MGI:1931352)			
chr11	57528462	57542504	11q12.1-q12.3	11q12.1		602251	"TIMM10, TIM10A, TIM10"	"Translocase of inner mitochondrial membrane 10, yeast, homolog of"	TIMM10	26519	ENSG00000134809			Timm10 (MGI:1353429)			
chr11	57536840	57550273	11q12.1	11q12.1		613664	"SMTNL1, CHASM"	Smoothelin-like 1	SMTNL1	219537	ENSG00000214872			Smtnl1 (MGI:1915928)			
chr11	57551654	57568329	11q12	11q12.1		603890	"UBE2L6, UBCH8"	Ubiquitin-conjugating enzyme E2L 6	UBE2L6	9246	ENSG00000156587			Ube2l6 (MGI:1914500)			
chr11	57597553	57614852	11q11-q13.1	11q12.1		606860	"C1NH, HAE1, HAE2, SERPING1"	Complement component-1 inhibitor	SERPING1	710	ENSG00000149131		"Angioedema, hereditary, types I and II, 106100 (3), Autosomal recessive, Autosomal dominant; Complement component 4, partial deficiency of, 120790 (3), Autosomal dominant"	Serping1 (MGI:894696)			
chr11	57641197	57641285	11q12	11q12.1		610175	"MIR130A, MIRN130A"	Micro RNA 130A	MIR130A	406919							
chr11	57645086	57649943	11q12.1	11q12.1		609725	YPEL4	Yippee-like 4	YPEL4	219539	ENSG00000166793			Ypel4 (MGI:3605071)			
chr11	57657743	57661864	11q12.1	11q12.1		608757	"CLP1, HEAB, PCH10"	"Cleavage and polyadenylation factor I subunit 1, yeast, homolog of"	CLP1	10978	ENSG00000172409		"Pontocerebellar hypoplasia, type 10, 615803 (3), Autosomal recessive"	Clp1 (MGI:2138968)			
chr11	57668001	57701186	11q12.1	11q12.1		614586	"ZDHHC5, DHHC5, ZNF375, KIAA1748"	Zinc finger DHHC domain-containing protein 5	ZDHHC5	25921	ENSG00000156599			Zdhhc5 (MGI:1923573)			
chr11	57703708	57712526	11q12.1	11q12.1		612385	MED19	Mediator complex subunit 19	MED19	219541	ENSG00000156603			Med19 (MGI:1914234)			
chr11	57712522	57740972	11cen-q22.3	11q12.1		616715	TMX2	Thioredoxin-related transmembrane protein 2	TMX2	51075	ENSG00000213593			Tmx2 (MGI:1914208)			
chr11	57741249	57743553	11q12.1	11q12.1		607914	"SELENOH, SELH"	Selenoprotein H	SELENOH	280636	ENSG00000211450			Selenoh (MGI:1919907)			
chr11	57761761	57819179	11q11	11q12.1		601045	"CTNND1, CTNND, BCDS2"	"Catenin (cadherin-associated protein), delta 1"	CTNND1	1500	ENSG00000198561		"Blepharocheilodontic syndrome 2, 617681 (3), Autosomal dominant"	Ctnnd1 (MGI:105100)			
chr11	58526870	58578238	11q12.1	11q12.1		605390	LPXN	Leupaxin	LPXN	9404	ENSG00000110031			Lpxn (MGI:2147677)			
chr11	58622672	58625732	11q12.2	11q12.1		118945	CNTF	Ciliary neurotrophic factor	CNTF	1270	ENSG00000242689			Cntf (MGI:88439)			
chr11	58708756	58731973	11q12.1	11q12.1		607424	"GLYAT, ACGNAT, CAT"	Glycine-N-acyltransferase	GLYAT	10249	ENSG00000149124			Glyat (MGI:2147502)			
chr11	58834064	58905839	11q12.1	11q12.1		614762	GLYATL2	Glycine N-acyltransferase-like 2	GLYATL2	219970	ENSG00000156689						
chr11	58905397	58957073	11q12.1	11q12.1		614761	GLYATL1	Glycine-N-acyltransferase-like 1	GLYATL1	92292	ENSG00000166840						
chr11	59107184	59127414	11q12.1	11q12.1		615584	"FAM111B, POIKTMP"	"Family with sequence similarity 111, member B"	FAM111B	374393	ENSG00000189057		"Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis, 615704 (3), Autosomal dominant"				
chr11	59142745	59155038	11q12.1	11q12.1		615292	"FAM111A, KIAA1895, KCS2, GCLEB"	"Family with sequence similarity 111, member A"	FAM111A	63901	ENSG00000166801		"Gracile bone dysplasia, 602361 (3), Autosomal dominant; Kenny-Caffey syndrome, type 2, 127000 (3), Autosomal dominant"	Fam111a (MGI:1915508)			
chr11	59171429	59208586	11q12.1	11q12.1		616110	"DTX4, RNF155, KIAA0937"	"Deltex, Drosoophila, homolog of, 4"	DTX4	23220	ENSG00000110042			Dtx4 (MGI:2672905)			
chr11	59208509	59213020	11q12.1	11q12.1		610390	"MPEG1, MPG1"	Macrophage expressed gene 1	MPEG1	219972	ENSG00000197629			Mpeg1 (MGI:1333743)			
chr11	59364458	59365393	11q12.1	11q12.1		615702	OR5AN1	"Olfactory receptor, family 5, subfamily AN, member 1"	OR5AN1	390195	ENSG00000176495			Olfr1434 (MGI:3031268)			
chr11	59574397	59616143	11q12.1	11q12.1		167040	OSBP	Oxysterol-binding protein	OSBP	5007	ENSG00000110048			Osbp (MGI:97447)			
chr11	59636715	59669037	11q12.1	11q12.1		614660	"PATL1, PAT1B"	"Protein associated with topoisomerase II, S. cerevisiae, homolog of, 1"	PATL1	219988	ENSG00000166889			Patl1 (MGI:2147679)			
chr11	59755058	59805881	11q12.1	11q12.1		600876	"STX3, STX3A"	Syntaxin 3	STX3	6809	ENSG00000166900			Stx3 (MGI:103077)			
chr11	59806134	59810871	11q12-q13.1	11q12.1		611829	MRPL16	Mitochondrial ribosomal protein L16	MRPL16	54948	ENSG00000166902			Mrpl16 (MGI:2137219)			
chr11	59829267	59845500	11q13	11q12.1		609342	"GIF, IF"	Gastric intrinsic factor	GIF	2694	ENSG00000134812		"Intrinsic factor deficiency, 261000 (3), Autosomal recessive"	Gif (MGI:1202394)			
chr11	59852807	59866567	11q11-q12	11q12.1		189905	"TCN1, TC1"	Transcobalamin I	TCN1	6947	ENSG00000134827						
chr11	60056627	60071115	11q12-q13	11q12.1		606498	"MS4A3, HTM4, CD20L"	"Membrane-spanning 4-domains, subfamily A, member 3"	MS4A3	932	ENSG00000149516			Ms4a3 (MGI:2158468)			
chr11	60088260	60098466	11q13	11q12.1		147138	"MS4A2, FCER1B"	"Membrane-spanning 4-domains, subfamily A, member 2 (Fc fragment of IgE, high affinity I, receptor for, beta polypeptide)"	MS4A2	2206	ENSG00000149534		"{Atopy, susceptibility to}, 147050 (3), Autosomal dominant"	Ms4a2 (MGI:95495)			
chr11	60171606	60184665	11q12-q13	11q12.2		606548	"MS4A6A, MS4A6"	"Membrane-spanning 4-domains, subfamily A, member 6A"	MS4A6A	64231	ENSG00000110077			Ms4a6d (MGI:1916024)			
chr11	60201252	60243123	11q12-q13.1	11q12.2		608401	MS4A4E	"Membrane-spanning 4-domains, subfamily A, member 4E"	MS4A4E	643680	ENSG00000214787						
chr11	60280540	60308971	11q12-q13	11q12.2		606547	"MS4A4A, MS4A4"	"Membrane-spanning 4-domains, subfamily A, member 4A"	MS4A4A	51338	ENSG00000110079			Ms4a4a (MGI:3643932)			
chr11	60334881	60340967	11q12-q13.1	11q12.2		608402	MS4A6E	"Membrane-spanning 4-domains, subfamily A, member 6E"	MS4A6E	245802	ENSG00000166926						
chr11	60378484	60395953	11q12-q13	11q12.2		606502	"MS4A7, CFFM4"	"Membrane-spanning 4-domains, subfamily A, member 7"	MS4A7	58475	ENSG00000166927			Ms4a7 (MGI:1918846)			
chr11	60429588	60447791	11q12-q13	11q12.2		606499	"MS4A5, TETM4, CD20L2"	"Membrane-spanning 4-domains, subfamily A, member 5"	MS4A5	64232	ENSG00000166930			Ms4a5 (MGI:2670985)			
chr11	60455808	60470751	11q13	11q12.2		112210	"MS4A1, CD20, CVID5"	"Membrane-spanning 4-domains, subfamily A, member 1"	MS4A1	931	ENSG00000156738		"Immunodeficiency, common variable, 5, 613495 (3), Autosomal recessive"	Ms4a1 (MGI:88321)			
chr11	60492742	60507429	11q12-q13	11q12.2		606550	MS4A12	"Membrane-spanning 4-domains, subfamily A, member 12"	MS4A12	54860	ENSG00000071203			Ms4a12 (MGI:2685812)			
chr11	60699573	60715810	11q12-q13	11q12.2		606549	MS4A8B	"Membrane-spanning 4-domains, subfamily A, member 8B"	MS4A8	83661	ENSG00000166959			Ms4a8a (MGI:1927657)			
chr11	60785331	60801304	11q12-q13.1	11q12.2		608403	MS4A10	"Membrane-spanning 4-domains, subfamily A, member 10"	MS4A10	341116	ENSG00000172689			Ms4a10 (MGI:1917076)			
chr11	60841955	60851087	11q12	11q12.2		611293	"CCDC86, CYCLON"	Coiled-coil domain-containing protein 86	CCDC86	79080	ENSG00000110104			Ccdc86 (MGI:1277220)			
chr11	60850924	60855970	11q12.2	11q12.2		604837	"PTGDR2, GPR44"	Prostaglandin D2 receptor 2	PTGDR2	11251	ENSG00000183134			Ptgdr2 (MGI:1330275)			
chr11	60867541	60875692	11q12.2	11q12.2		195000	"ZP1, OOMD1"	Zona pellucida glycoprotein 1	ZP1	22917	ENSG00000149506		"Oocyte maturation defect 1, 615774 (3), Autosomal recessive"	Zp1 (MGI:103073)			
chr11	60890546	60906588	11q12.2	11q12.2		608330	"PRPF19, PRP19, PSO4, NMP200"	"Precursor mRNA-processing factor 19, S. cerevisiae, homolog of"	PRPF19	27339	ENSG00000110107			Prpf19 (MGI:106247)			
chr11	60924440	60937158	11q12.2	11q12.2		617363	"TMEM132A, KIAA1583"	Transmembrane protein 132A	TMEM132A	54972	ENSG00000006118			Tmem132a (MGI:2147810)			
chr11	60937082	60952080	11q12	11q12.2		610408	"SLC15A3, PHT2"	"Solute carrier family 15 (oligopeptide transporter), member 3"	SLC15A3	51296	ENSG00000110446			Slc15a3 (MGI:1929691)			
chr11	60971640	61020376	Chr.11	11q12.2		186720	"CD6, TP120"	CD6 antigen	CD6	923	ENSG00000013725			Cd6 (MGI:103566)			
chr11	61093962	61127851	11q13	11q12.2		153340	"CD5, LEU1"	CD5 antigen (p56-62)	CD5	921	ENSG00000110448			Cd5 (MGI:88340)			
chr11	61130255	61161443	11q12.2	11q12.2		610038	VPS37C	"Vacuolar protein sorting 37, yeast, homolog of, C"	VPS37C	55048	ENSG00000167987			Vps37c (MGI:2147661)			
chr11	61222348	61231694	11q13	11q12.2		169720	PGA4	Pepsinogen A4	PGA4	643847	ENSG00000229183						
chr11	61241175	61251443	11q13	11q12.2		169730	PGA5	Pepsinogen A5	PGA5	5222	ENSG00000256713	pter-5'HRAS--5'INS--cen					
chr11	61258285	61295315	11q11	11q12.2		611115	"VWC1, URG11"	von Willebrand factor C and EGF domain-containing protein	VWCE	220001	ENSG00000167992			Vwce (MGI:1919018)			
chr11	61299446	61333211	11q12-q13	11q12.2		600045	DDB1	"Damage-specific DNA binding protein 1, 127kD"	DDB1	1642	ENSG00000167986			Ddb1 (MGI:1202384)			
chr11	61333181	61353425	11q12.2	11q12.2		615844	DAK	"Dihydroxyacetone kinase 2, S. cerevisiae, homolog of"	TKFC	26007	ENSG00000149476			Tkfc (MGI:2385084)			
chr11	61362000	61378223	11q12.2	11q12.2		614459	"TMEM138, JBTS16"	Transmembrane protein 138	TMEM138	51524	ENSG00000149483		"Joubert syndrome 16, 614465 (3), Autosomal recessive"	Tmem138 (MGI:1920232)			
chr11	61391981	61398862	11q12.2	11q12.2		613277	"TMEM216, JBTS2, CORS2, MKS2"	Transmembrane protein 216	TMEM216	51259	ENSG00000187049		"Joubert syndrome 2, 608091 (3), Autosomal recessive; Meckel syndrome 2, 603194 (3), Autosomal recessive"	Tmem216 (MGI:1920020)			
chr11	61430124	61446766	11q13.1	11q12.2		613019	"SDHAF2, SDH5, PGL2"	Succinate dehydrogenase complex assembly factor 2	SDHAF2	54949	ENSG00000167985		"Paragangliomas 2, 601650 (3), Autosomal dominant"	Sdhaf2 (MGI:1913322)			
chr11	61513715	61588403	11q13	11q12.2		604146	SYT7	Synaptotagmin 7	SYT7	9066	ENSG00000011347			Syt7 (MGI:1859545)			
chr11	61680183	61747001	11q12.2	11q12.2		614015	"DAGLA, KIAA0659"	"Diacylglycerol lipase, alpha"	DAGLA	747	ENSG00000134780			Dagla (MGI:2677061)			
chr11	61752616	61788517	11q12-q13.1	11q12.2		608329	"C11orf9, KIAA0954"	Chromosome 11 open reading frame 9	MYRF	745	ENSG00000124920			Myrf (MGI:2684944)			
chr11	61789129	61792612	11q12	11q12.2		617615	"TMEM258, C11orf10"	Transmembrane protein 258	TMEM258	746	ENSG00000134825			Tmem258 (MGI:1916288)			
chr11	61792636	61797243	11q12	11q12.2		600393	FEN1	Flap structure-specific endonuclease 1	FEN1	2237	ENSG00000168496			Fen1 (MGI:102779)			
chr11	61799624	61817056	11q12-q13.1	11q12.2		606148	FADS1	Fatty acid desaturase 1	FADS1	3992	ENSG00000149485			Fads1 (MGI:1923517)			
chr11	61816202	61867353	11q12-q13.1	11q12.2		606149	FADS2	Fatty acid desaturase 2	FADS2	9415	ENSG00000134824			Fads2 (MGI:1930079)			
chr11	61873522	61892223	11q12-q13.1	11q12.2		606150	FADS3	Fatty acid desaturase 3	FADS3	3995	ENSG00000221968			Fads3 (MGI:1928740)			
chr11	61946721	61964464	11q13	11q12.3		607854	"BEST1, VMD2, ARB, RP50"	Bestrophin 1	BEST1	7439	ENSG00000167995		"Bestrophinopathy, autosomal recessive, 611809 (3); Macular dystrophy, vitelliform, 2, 153700 (3), Autosomal dominant; Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma, 193220 (3), Autosomal dominant; Retinitis pigmentosa, concentric, 613194 (3); Retinitis pigmentosa-50, 613194 (3); Vitreoretinochoroidopathy, 193220 (3), Autosomal dominant"	Best1 (MGI:1346332)			
chr11	61964284	61967659	11q12-q13	11q12.3		134770	"FTH1, FTHL6, HFE5"	"Ferritin, heavy polypeptide 1"	FTH1	2495	ENSG00000167996	mutation identified in 1 family	"?Hemochromatosis, type 5, 615517 (3), Autosomal dominant"	Fth1 (MGI:95588)			
chr11	62123972	62155473	11q12.3	11q12.3		604411	INCENP	Inner centromere protein	INCENP	3619	ENSG00000149503			Incenp (MGI:1313288)			
chr11	62190237	62193536	11q12.3	11q12.3		615060	"SCGB1D1, LPNA"	"Secretoglobin, family 1D, member 1"	SCGB1D1	10648	ENSG00000168515	previously mapped to 15q12-q13					
chr11	62208667	62213938	11q12.3	11q12.3		604398	"SCGB2A1, MGB2, LPNC"	"Secretoglobin, family 2A, member 1 (mammaglobin 2)"	SCGB2A1	4246	ENSG00000124939						
chr11	62242251	62244807	11q12.3	11q12.3		615061	"SCGB1D2, LPNB"	"Secretoglobin, family 1D, member 2"	SCGB1D2	10647	ENSG00000124935	previously mapped to 10q23					
chr11	62270129	62273159	11q12.3-q13.1	11q12.3		605562	"MGB1, SCGB2A2"	"Mammaglobin 1 (secretoglobin, family 2A, member 2)"	SCGB2A2	4250	ENSG00000110484						
chr11	62296281	62299063	11q12.3	11q12.3		615062	"SCGB1D4, IIS"	"Secretoglobin, family 1D, member 4"	SCGB1D4	404552	ENSG00000197745						
chr11	62419034	62423205	11q12.3-q13.1	11q12.3		192020	"SCGB1A1, UGB, CC10, CCSP"	"Secretoglobin, family 1A, member 1 (uteroglobin)"	SCGB1A1	7356	ENSG00000149021			Scgb1a1 (MGI:98919)			
chr11	62433541	62546859	11q12-q13	11q12.3		103390	AHNAK	AHNAK nucleoprotein (desmoyokin)	AHNAK	79026	ENSG00000124942			Ahnak (MGI:1316648)			
chr11	62559600	62573987	11q12.3	11q12.3		130593	"EEF1G, EF1G"	"Eukaryotic translation elongation factor 1, gamma"	EEF1G	1937	ENSG00000254772			Eef1g (MGI:1914410)			
chr11	62593202	62601839	11q12-q13.1	11q12.3		603947	"MTA2, MTA1L1"	Metastasis-associated protein 2	MTA2	9219	ENSG00000149480			Mta2 (MGI:1346340)			
chr11	62612740	62615119	11q13	11q12.3		180721	"ROM1, ROSP1, RP7"	Rod outer segment membrane protein-1	ROM1	6094	ENSG00000149489	digenic RP with RDS	"Retinitis pigmentosa 7, digenic, 608133 (3), Autosomal recessive, Autosomal dominant"	Rom1 (MGI:97998)			
chr11	62615295	62622174	11q12-q13	11q12.3		606374	"B3GAT3, GLCATI, JDSCD"	"Beta-1,3-glucuronyltransferase 3"	B3GAT3	26229	ENSG00000149541	pseudogene on chr.3	"Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects, 245600 (3), Autosomal recessive"	B3gat3 (MGI:1919977)			
chr11	62624825	62646725	11q13-qter	11q12.3		104160	"GANAB, PKD3"	Neutral alpha-glucosidase AB	GANAB	23193	ENSG00000089597		"Polycystic kidney disease 3, 600666 (3), Autosomal dominant"	Ganab (MGI:1097667)			
chr11	62646847	62653301	11q12.3	11q12.3		611349	"INTS5, INT5, KIAA1698"	Integrator complex subunit 5	INTS5	80789	ENSG00000185085			Ints5 (MGI:1923578)			
chr11	62665252	62667450	11q12.3	11q12.3		617897	"CSKMT, METTL12"	Citrate synthase lysine methyltransferase	CSKMT	751071	ENSG00000214756						
chr11	62671653	62673689	11q12.3	11q12.3		616097	"UQCC3, C11orf83, MC3DN9"	Ubiquinol-cytochrome C reductase complex assembly factor 3	UQCC3	790955	ENSG00000204922	mutation identified in 1 MC3DN9 patient	"?Mitochondrial complex III deficiency, nuclear type 9, 616111 (3), Autosomal recessive"	Uqcc3 (MGI:2147553)			
chr11	62676497	62679116	11q12.3	11q12.3		616378	"UBXN1, SAKS1"	UBX domain protein 1	UBXN1	51035	ENSG00000162191			Ubxn1 (MGI:1289301)			
chr11	62690261	62709618	11q13	11q12.3		606158	"BSCL2, SPG17, HMN5, PELD"	Seipin	BSCL2	26580	ENSG00000168000		"Encephalopathy, progressive, with or without lipodystrophy, 615924 (3), Autosomal recessive; Lipodystrophy, congenital generalized, type 2, 269700 (3), Autosomal recessive; Neuropathy, distal hereditary motor, type VA, 600794 (3), Autosomal dominant; Silver spastic paraplegia syndrome, 270685 (3), Autosomal dominant"	Bscl2 (MGI:1298392)			
chr11	62761538	62766714	11q13.1	11q12.3		602013	POLR2G	Polymerase (RNA) II (DNA directed) polypeptide G	POLR2G	5436	ENSG00000168002			Polr2g (MGI:1914960)			
chr11	62792124	62805491	11q12-q13	11q12.3		602647	"NXF1, TAP, MEX67"	Nuclear RNA export factor 1	NXF1	10482	ENSG00000162231			Nxf1 (MGI:1858330)			
chr11	62806859	62832090	11q12.3	11q12.3		603189	"STX5, STX5A"	Syntaxin 5	STX5	6811	ENSG00000162236			Stx5a (MGI:1928483)			
chr11	62851977	62855884	11q13	11q12.3		603222	"UHG, U22HG"	U22 host gene	SNHG1	23642							
chr11	62852909	62853034	11q13	11q12.3		603223	RNU22	"RNA, U22 small nucleolar"	SNORD22	9304							
chr11	62853325	62853392	11q13	11q12.3		603230	RNU31	"RNA, U31 small nucleolar"	SNORD31	9298							
chr11	62853662	62853731	11q13	11q12.3		603229	RNU30	"RNA, U30 small nucleolar"	SNORD30	9299							
chr11	62853903	62853967	11q13	11q12.3		603228	RNU29	"RNA, U29 small nucleolar"	SNORD29	9297							
chr11	62854620	62854694	11q13	11q12.3		603227	RNU28	"RNA, U28 small nucleolar"	SNORD28	9300							
chr11	62855011	62855082	11q13	11q12.3		603226	RNU27	"RNA, U27 small nucleolar"	SNORD27	9301							
chr11	62855291	62855365	11q13	11q12.3		603225	RNU26	"RNA, U26 small nucleolar"	SNORD26	9302							
chr11	62855564	62855630	11q13	11q12.3		603224	RNU25	"RNA, U25 small nucleolar"	SNORD25	9303							
chr11	62856011	62888882	11q13	11q12.3		158070	"SLC3A2, MDU1, NACAE"	"Solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2"	SLC3A2	6520	ENSG00000168003	prob. 11q13		Slc3a2 (MGI:96955)			
chr11	62908674	62921860	11q13	11q12.3		118510	CHRM1	"Cholinergic receptor, muscarinic, 1"	CHRM1	1128	ENSG00000168539			Chrm1 (MGI:88396)			
chr11	62976596	62985022	11q13.1-q13.2	11q12.3		607582	"SLC22A6, OAT1, PAHT"	"Solute carrier family 22 (organic anion transporter), member 6"	SLC22A6	9356	ENSG00000197901			Slc22a6 (MGI:892001)			
chr11	62992823	63015844	Chr.11	11q12.3		607581	"SLC22A8, OAT3"	"Solute carrier family 22 (organic anion transporter), member 8"	SLC22A8	9376	ENSG00000149452			Slc22a8 (MGI:1336187)			
chr11	63079939	63144220	11q12.3	11q12.3		611698	SLC22A24	"Solute carrier family 22, member 24"	SLC22A24	283238	ENSG00000197658			Slc22a19 (MGI:2442751)			
chr11	63162263	63243522	11q12.3	11q12.3		610792	UST6	Organic anion transporter UST6	SLC22A25	387601	ENSG00000196600			"Slc22a29,Slc22a28,Slc22a27,Slc22a30 (MGI:2442750,MGI:3645714,MGI:3605624,MGI:3042283)"			
chr11	63268256	63311982	11q12.3	11q12.3		607580	"SLC22A10, OAT5"	"Solute carrier family 22 (organic anion/cation transporter), member 10"	SLC22A10	387775	ENSG00000184999						
chr11	63368870	63410877	11q12.3	11q12.3		607579	"SLC22A9, OAT4, UST3"	"Solute carrier family 22 (organic anion/cation transporter), member 9"	SLC22A9	114571	ENSG00000149742						
chr11	63506051	63516773	11q13	11q12.3		606096	LGALS12	"Lectin, galactoside-binding, soluble, 12"	LGALS12	85329	ENSG00000133317			Lgals12 (MGI:1929094)			
chr11	63536800	63546457	11q23	11q12.3		605092	"RARRES3, TIG3"	Retinoic acid receptor responder 3	RARRES3	5920	ENSG00000133321						
chr11	63552758	63565071	11q12.3	11q12.3		613866	HRASLS2	HRAS-like suppressor 2	HRASLS2	54979	ENSG00000133328						
chr11	63574461	63616925	11q12.3-q13.1	11q12.3-q13.1		613867	"PLA2G16, HRASLS3, HRSL3, HREV107"	"Phospholipase A2, group XVI"	PLA2G16	11145	ENSG00000176485			Pla2g16 (MGI:2179715)			
chr11	63600000	77400000	11q13			617697	CUPID2	"CCND1 upstream intergenic DNA repair 2, noncoding"									
chr11	63600000	110600000	11q13-q22			133220	ESA4	Esterase-A4	ESA4	2090							
chr11	63600000	77400000	11q13			611958	HPC14	"Prostate cancer, hereditary, 14"		100188867		associated with rs7931342	"{Prostate cancer, hereditary, 14}, 611958 (2)"				
chr11	63600000	77400000	11q13			600319	IDDM4	Insulin-dependent diabetes mellitus-4	IDDM4	3403			"{Diabetes mellitus, insulin-dependent, 4}, 600319 (2)"				
chr11	63600000	77400000	11q13			166750	"OTDD, DEL11q13, C11DELq13"	Otodental dysplasia (chromosome 11q13 deletion syndrome)				between rs9666584 and rs41408348	"Otodental dysplasia chromosome deletion syndrome, 166750 (4), Autosomal dominant"				
chr11	63600000	77400000	11q13			169710	PGA3	Pepsinogen A3	PGA3	643834	ENSG00000229859						
chr11	63600000	77400000	11q13			165110	SEA	Oncogene SEA (S13 avian erythroblastosis)	SEA	6395							
chr11	63600000	77400000	11q13			607088	SMAR	"Spinal muscular atrophy, chronic distal, autosomal recessive"		246751		no mutations found in IGHMBP2	"Spinal muscular atrophy, chronic distal, autosomal recessive, 607088 (2), Autosomal recessive"				
chr11	63600000	77400000	11q13			191181	ST3	"Suppression of tumorigenicity-3 (tumor-suppressor gene, HELA cell type)"	ST3	6762			"Cervical carcinoma, 191181 (2)"				
chr11	63624081	63671973	11q13.1	11q13.1		609369	"ATL3, HSN1F"	Atlastin 3	ATL3	25923	ENSG00000184743		"Neuropathy, hereditary sensory, type IF, 615632 (3), Autosomal dominant"	Atl3 (MGI:1924270)			
chr11	63681314	63759890	11q13	11q13.1		604249	"RTN3, NSPL2"	Reticulon 3	RTN3	10313	ENSG00000133318	pseudogene on chr.4		Rtn3 (MGI:1339970)			
chr11	63759891	63768641	11q13	11q13.1		615699	C11orf95	Chromosome 11 open reading frame 95	C11orf95	65998	ENSG00000188070			2700081O15Rik (MGI:1919667)			
chr11	63838927	63911019	11q12-q13	11q13.1		600526	"MARK2, EMK1"	MAP/microtubule affinity-regulating kinase 2	MARK2	2011	ENSG00000072518			Mark2 (MGI:99638)			
chr11	63911220	63916843	11q13.1	11q13.1		616019	RCOR2	Rest corepressor 2	RCOR2	283248	ENSG00000167771			Rcor2 (MGI:1859854)			
chr11	63974606	63976542	11q13	11q13.1		123870	COX8A	"Cytochrome c oxidase, subunit VIIIA"	COX8A	1351	ENSG00000176340	mutation identified in 1 COX4D patient	"?Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Cox8a (MGI:105959)			
chr11	63985852	63998419	11q13.1	11q13.1		608337	"OTUB1, OTU1, OTB1"	OTU domain-containing ubiquitin aldehyde-binding protein 1	OTUB1	55611	ENSG00000167770						
chr11	63998553	64166651	11q13.1	11q13.1		610400	"MACROD1, LRP16"	Macro domain-containing 1	MACROD1	28992	ENSG00000133315			Macrod1 (MGI:2147583)			
chr11	64035969	64127288	11q12-q13	11q13.1		604806	FLRT1	Fibronectin-like domain-containing leucine-rich transmembrane protein-1	FLRT1	23769	ENSG00000126500			Flrt1 (MGI:3026647)			
chr11	64185271	64204547	11q13	11q13.1		605063	"STIP1, HOP"	Stress-induced phosphoprotein 1	STIP1	10963	ENSG00000168439			Stip1 (MGI:109130)			
chr11	64206661	64223890	11q12	11q13.1		607901	"KIND3, URP2, MIG2B, FERMT3"	Kindlin 3	FERMT3	83706	ENSG00000149781		"Leukocyte adhesion deficiency, type III, 612840 (3), Autosomal recessive"	Fermt3 (MGI:2147790)			
chr11	64223798	64226253	11q13	11q13.1		610470	TRPT1	Transfer RNA phosphotransferase 1	TRPT1	83707	ENSG00000149743			Trpt1 (MGI:1333115)			
chr11	64230280	64234280	11q13	11q13.1		604189	"DANJC4, HSPF2"	"DnaJ, E. coli, homolog of, subfamily C, member 4 (heat-shock 40kD protein 2)"	DNAJC4	3338	ENSG00000110011			Dnajc4 (MGI:1927346)			
chr11	64234583	64239263	11q13	11q13.1		601398	"VEGFB, VRF"	Vascular endothelial growth factor B	VEGFB	7423	ENSG00000173511			Vegfb (MGI:106199)			
chr11	64240940	64244134	11q13.1-q13.3	11q13.1		186946	FKBP2	"FK506-binding protein-2, 13kD"	FKBP2	2286	ENSG00000173486			Fkbp2 (MGI:95542)			
chr11	64244478	64246940	11q13	11q13.1		601140	"PPP1R14B, PLCB3N, PNG"	"Protein phosphatase 1, regulatory subunit 14B"	PPP1R14B	26472	ENSG00000173457			Ppp1r14b (MGI:107682)			
chr11	64251522	64269451	11q13	11q13.1		600230	PLCB3	"Phospholipase C, beta 3 (phosphatidylinositol-specific)"	PLCB3	5331	ENSG00000149782	within 900kb of MEN1		Plcb3 (MGI:104778)			
chr11	64269827	64284703	11q13.1	11q13.1		603167	"BAD, BCL2L8"	BCL1 antagonist of cell death	BAD	572	ENSG00000002330			Bad (MGI:1096330)			
chr11	64291301	64300030	11q13	11q13.1		605720	"KCNK4, TRAAK"	"Potassium channel, subfamily K, member 4"	KCNK4	50801	ENSG00000182450			Kcnk4 (MGI:1298234)			
chr11	64300390	64304766	11q13.1	11q13.1		617511	"CATSPERZ, TEX40"	"Cation channel, sperm-associated, auxiliary subunit zeta"	CATSPERZ	25858	ENSG00000219435			Catsperz (MGI:1914327)			
chr11	64305527	64316742	11q12	11q13.1		601998	"ESRRA, ESRL1"	"Estrogen-related receptor, alpha"	ESRRA	2101	ENSG00000173153						
chr11	64318087	64321822	11q13	11q13.1		606583	"PRDX5, AOEB166"	Peroxiredoxin 5	PRDX5	25824	ENSG00000126432			Prdx5 (MGI:1859821)			
chr11	64340202	64357533	11q13.1	11q13.1		611205	"CCDC88B, GIPIE"	Coiled-coil domain-containing protein 88B	CCDC88B	283234	ENSG00000168071			Ccdc88b (MGI:1925567)			
chr11	64359152	64372214	11q13.1	11q13.1		603606	"RPS6KA4, RSKB, MSK2"	"Ribosomal protein S6 kinase, 90kD, 4"	RPS6KA4	8986	ENSG00000162302			Rps6ka4 (MGI:1930076)			
chr11	64555600	64572874	11q13	11q13.1		607097	"SLC22A11, OAT4"	"Solute carrier family 22 (organic anion/cation transporter), member 11"	SLC22A11	55867	ENSG00000168065						
chr11	64590809	64603249	11q13	11q13.1		607096	"SLC22A12, OAT4L, URAT1"	"Solute carrier family 22 (urate transporter), member 12"	SLC22A12	116085	ENSG00000197891		"Hypouricemia, renal, 220150 (3), Autosomal recessive"	Slc22a12 (MGI:1195269)			
chr11	64606173	64723187	11q13	11q13.1		600566	NRXN2	Neurexin 2	NRXN2	9379	ENSG00000110076			Nrxn2 (MGI:1096362)			
chr11	64726910	64745480	11q13	11q13.1		605577	"RASGRP2, CDC25L"	Ras guanyl nucleotide-releasing protein 2	RASGRP2	10235	ENSG00000068831	mutation identified in 1 BDPLT18 family	"?Bleeding disorder, platelet-type, 18, 615888 (3), Autosomal recessive"	Rasgrp2 (MGI:1333849)			
chr11	64746388	64760714	11q13	11q13.1		608455	PYGM	"Phosphorylase, glycogen, muscle"	PYGM	5837	ENSG00000068976		"McArdle disease, 232600 (3), Autosomal recessive"	Pygm (MGI:97830)			
chr11	64764603	64778843	11q13	11q13.1		601516	"SF1, ZNF162, D11S636, ZFM1"	Splicing factor 1 (zinc finger protein-162)	SF1	7536	ENSG00000168066						
chr11	64786913	64803253	11q13	11q13.1		603166	"MAP4K2, RAB8IP, GCK"	Mitogen-activating protein kinase kinase kinase kinase 2 (RAB8-interacting protein; germinal center kinase)	MAP4K2	5871	ENSG00000168067			Map4k2 (MGI:1346883)			
chr11	64803513	64811293	11q13	11q13.1		613733	MEN1	Menin	MEN1	4221	ENSG00000133895	linked distal to PYGM	"Adrenal adenoma, somatic (3); Angiofibroma, somatic (3); Carcinoid tumor of lung (3); Lipoma, somatic (3); Multiple endocrine neoplasia 1, 131100 (3), Autosomal dominant; Parathyroid adenoma, somatic (3)"	Men1 (MGI:1316736)			
chr11	64823808	64844685	11q13	11q13.1		613991	"CDC42BPG, MRCKG"	"CDC42-binding protein kinase, gamma"	CDC42BPG	55561	ENSG00000171219			Cdc42bpg (MGI:2652845)			
chr11	64852726	64879712	11q13	11q13.1		605888	EHD1	EH domain-containing 1 protein	EHD1	10938	ENSG00000110047			Ehd1 (MGI:1341878)			
chr11	64891136	64891245	11q13.1	11q13.1		610939	"MIR192, MIRN192"	Micro RNA 192	MIR192	406967							
chr11	64891354	64891438	11q13.1	11q13.1		610941	"MIR194-2, MIRN194-2"	Micro RNA 194-2	MIR194-2	406970							
chr11	64894531	64917249	11q13.1	11q13.1		616225	"ATG2A, KIAA0404"	"Autophagy 2, S. cerevisiae, homolog of, A"	ATG2A	23130	ENSG00000110046			Atg2a (MGI:1916291)			
chr11	64917552	64934477	11q13	11q13.1		601644	PPP2R5B	"Protein phosphatase-2, regulatory subunit B (B56), beta isoform"	PPP2R5B	5526	ENSG00000068971			Ppp2r5b (MGI:2388480)			
chr11	64934470	64938130	11q13.1	11q13.1		609651	"GPHA2, GPA2"	"Glycoprotein hormone, alpha-2"	GPHA2	170589	ENSG00000149735			Gpha2 (MGI:2156541)			
chr11	64938229	64972097	11q13.1	11q13.1		617130	"MAJIN, C11orf85"	Membrane-anchored junction protein	MAJIN	283129	ENSG00000168070			Majin (MGI:1923913)			
chr11	64987944	64997044	11q13.1	11q13.1		614983	"BATF2, SARI"	"Basic leucine zipper transcription factor, ATF-like 2"	BATF2	116071	ENSG00000168062			Batf2 (MGI:1921731)			
chr11	65014112	65022184	11q13	11q13.1		601175	ARL2	ADP=ribosylation factor-like 2	ARL2	402	ENSG00000213465			Arl2 (MGI:1928393)			
chr11	65027407	65040571	11q13	11q13.1		605964	SNX15	Sorting nexin 15	SNX15	29907	ENSG00000110025			Snx15 (MGI:1916274)			
chr11	65044817	65059019	11q12	11q13.1		602640	"NAALADL1, I100"	N-acetylated alpha-linked acidic dipeptidase-like 1	NAALADL1	10004	ENSG00000168060			Naaladl1 (MGI:2685810)			
chr11	65061008	65084142	11q13.1	11q13.1		609374	"CDCA5, SORORIN"	Cell division cycle-associated protein 5 (sororin)	CDCA5	113130	ENSG00000146670			Cdca5 (MGI:1915099)			
chr11	65096114	65111859	11q13.1	11q13.1		615738	"VPS51, ANG2"	"Vacuolar protein sorting 51, S. cerevisiae, homolog of"	VPS51	738	ENSG00000149823			Vps51 (MGI:1915755)			
chr11	65111853	65116234	11q13	11q13.1		603414	"TM7SF2, ANG1"	"Transmembrane 7 superfamily, member 2"	TM7SF2	7108	ENSG00000149809			Tm7sf2 (MGI:1920416)			
chr11	65116402	65117737	11q13	11q13.1		604575	"ZNHIT2, C11orf5, FON"	Zinc finger HIT domain containing protein 2	ZNHIT2	741	ENSG00000174276			Znhit2 (MGI:1352481)			
chr11	65120626	65122199	11q13	11q13.1		134690	FAU	Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV) ubiquitously expressed (fox derived)	FAU	2197	ENSG00000149806			Fau (MGI:102547)			
chr11	65122182	65127368	11q13	11q13.1		606866	"MRPL49, NOF1"	Mitochondrial ribosomal protein L49	MRPL49	740	ENSG00000149792			Mrpl49 (MGI:108180)			
chr11	65127278	65135177	11q13	11q13.1		608046	"SYVN1, HRD1, KIAA1810"	Synovial apoptosis inhibitor 1	SYVN1	84447	ENSG00000162298			Syvn1 (MGI:1921376)			
chr11	65170153	65173665	11q13.1	11q13.1		614030	"SPDYC, RINGOC"	"Speedy, xenopus, homolog of, C"	SPDYC	387778	ENSG00000204710						
chr11	65181214	65212005	11q13	11q13.1		114220	"CAPN1, SPG76"	"Calpain, large polypeptide L1"	CAPN1	823	ENSG00000014216		"Spastic paraplegia 76, autosomal recessive, 616907 (3), Autosomal recessive"	Capn1 (MGI:88263)			
chr11	65213839	65242756	11q13.1	11q13.1		611696	"SLC22A20, OAT6"	"Solute carrier family 22, member 20"	SLC22A20P	440044							
chr11	65314817	65322428	11q12-q13	11q13.1		606132	"CDC42EP2, CEP2, BORG1"	CDC42 effector protein 2	CDC42EP2	10435	ENSG00000149798			Cdc42ep2 (MGI:1929744)			
chr11	65333753	65354259	11q13	11q13.1		601671	"DPF2, REQ, UBID4"	"D4, zinc, and double PHD fingers family, member 2"	DPF2	5977	ENSG00000133884			Dpf2 (MGI:109529)			
chr11	65375191	65383700	11q13.1	11q13.1		610825	SLC25A45	"Solute carrier family 25, member 45"	SLC25A45	283130	ENSG00000162241			Slc25a45 (MGI:2147731)			
chr11	65422797	65445539	11q13.1	11q13.1		612769	"NEAT1, TNCRNA"	Noncoding nuclear-enriched abundant transcript 1	NEAT1	283131							
chr11	65497737	65506515	11q13.1	11q13.1		607924	"MALAT1, PRO1073"	Metastasis-associated lung adenocarcinoma transcript 1	MALAT1	378938		fused with TFEB in renal tumors					
chr11	65525076	65538710	11q13	11q13.1		607982	"SCYL1, NTKL, SCAR21"	SCY1-like 1	SCYL1	57410	ENSG00000142186		"Spinocerebellar ataxia, autosomal recessive 21, 616719 (3), Autosomal recessive"	Scyl1 (MGI:1931787)			
chr11	65538558	65558388	11q12	11q13.1		602090	"LTBP3, LTBP2, DASS, GPHYSD3"	Latent transforming growth factor beta binding protein-3	LTBP3	4054	ENSG00000168056		"Dental anomalies and short stature, 601216 (3), Autosomal recessive; Geleophysic dysplasia 3, 617809 (3), Autosomal dominant"	Ltbp3 (MGI:1101355)			
chr11	65572348	65574197	11q13.1	11q13.1		616128	"FAM89B, MTVR, LRAP25"	"Family with sequence similarity 89, member B"	FAM89B	23625	ENSG00000176973			Fam89b (MGI:106595)			
chr11	65592854	65595995	11q13	11q13.1		603940	KCNK7	"Potassium channel, subfamily K, member 7"	KCNK7	10089	ENSG00000173338			Kcnk7 (MGI:1341841)			
chr11	65597754	65614248	11q13.1-q13.3	11q13.1		600050	"MAP3K11, MLK3, PTK1, SPRK"	Mitogen-activated protein kinase kinase kinase 11	MAP3K11	4296	ENSG00000173327			Map3k11 (MGI:1346880)			
chr11	65614310	65637438	11q13.1	11q13.1		617657	PCNX3	"Pecanex, Drosophila, homolog of, 3"	PCNX3	399909	ENSG00000197136			Pcnx3 (MGI:1861733)			
chr11	65638106	65650929	11q13.3	11q13.1		602180	"SIPA1, SPA1"	Signal-induced proliferation-associated gene-1	SIPA1	6494	ENSG00000213445			Sipa1 (MGI:107576)			
chr11	65653595	65662971	11q12-q13	11q13.1		164014	"RELA, NFKB3"	v-rel avian reticuloendotheliosis viral oncogene homolog A (nuclear factor of kappa light polypeptide gene enhancer in B-cells 3 (p65))	RELA	5970	ENSG00000173039			Rela (MGI:103290)			
chr11	65712001	65719605	11q13	11q13.1		601409	"KAT5, HTATIP, TIP60, ESA1, PLIP"	K(lysine) acetyltransferase 5	KAT5	10524	ENSG00000172977			Kat5 (MGI:1932051)			
chr11	65717672	65720937	11q13.2	11q13.1		610330	"RNASEH2C, AYP1, FLJ20974, AGS3"	"Ribonuclease H2, subunit C"	RNASEH2C	84153	ENSG00000172922		"Aicardi-Goutieres syndrome 3, 610329 (3), Autosomal recessive"	Rnaseh2c (MGI:1915459)			
chr11	65773897	65780590	11q13.1	11q13.1		614367	"AP5B1, DKFZp761E198"	"Adaptor-related protein complex 5, beta-1 subunit"	AP5B1	91056	ENSG00000254470			Ap5b1 (MGI:2685808)			
chr11	65787033	65797218	11q13	11q13.1		602313	OVOL1	"Ovo, Drosophila, homolog-like, 1"	OVOL1	5017	ENSG00000172818			Ovol1 (MGI:1330290)			
chr11	65854810	65858332	11q13	11q13.1		601442	CFL1	Cofilin 1 (non-muscle)	CFL1	1072	ENSG00000172757			Cfl1 (MGI:101757)			
chr11	65860243	65867652	11q13	11q13.1		606591	MUS81	"Mus81, S. cerevisiae, homolog of"	MUS81	80198	ENSG00000172732			Mus81 (MGI:1918961)			
chr11	65866440	65872933	11q13	11q13.1		604633	"EFEMP2, FBLN4, UPH1, ARCL1B"	EGF-containing fibulin-like extracellular matrix protein 2 (fibulin 4)	EFEMP2	30008	ENSG00000172638		"Cutis laxa, autosomal recessive, type IB, 614437 (3), Autosomal recessive"	Efemp2 (MGI:1891209)			
chr11	65879812	65883740	11q13.1	11q13.1		602364	CTSW	Cathepsin W	CTSW	1521	ENSG00000172543			Ctsw (MGI:1338045)			
chr11	65883739	65888538	11q13.1	11q13.1		608296	"FIBP, TROFAS"	"Fibroblast growth factor, acidic, intracellular binding protein"	FIBP	9158	ENSG00000172500		"Thauvin-Robinet-Faivre syndrome, 617107 (3), Autosomal recessive"	Fibp (MGI:1926233)			
chr11	65890403	65891634	11q13.1	11q13.1		605360	DIPA	Delta antigen-interacting protein A	CCDC85B	11007	ENSG00000175602			Ccdc85b (MGI:2147607)			
chr11	65892135	65900525	11q13	11q13.1		136515	FOSL1	FOS-like antigen-1	FOSL1	8061	ENSG00000175592			Fosl1 (MGI:107179)			
chr11	65919256	65921576	11q13.1	11q13.1		602289	DRAP1	DR1-associated protein 1	DRAP1	10589	ENSG00000175550			Drap1 (MGI:1913806)			
chr11	65961688	65980135	Chr.11	11q13.1		605941	"SART1, HOMS1"	Squamous cell carcinoma antigen recognized by T cells 1	SART1	9092	ENSG00000175467			Sart1 (MGI:1309453)			
chr11	66002078	66004148	11q13.1	11q13.1		603811	"BANF1, BAF, NGPS"	Barrier to autointegration factor 1	BANF1	8815	ENSG00000175334		"Nestor-Guillermo progeria syndrome, 614008 (3), Autosomal recessive"	Banf1 (MGI:1346330)			
chr11	66011990	66013504	11q13	11q13.1		601891	CST6	Cystatin-M	CST6	1474	ENSG00000175315			Cst6 (MGI:1920970)			
chr11	66016751	66026517	11q13.1	11q13.1		606389	"CATSPER1, CATSPER, SPGF7"	"Cation channel, sperm-associated, 1"	CATSPER1	117144	ENSG00000175294		"Spermatogenic failure 7, 612997 (3), Autosomal recessive"	Catsper1 (MGI:2179947)			
chr11	66040764	66049179	11q13	11q13.1		608234	"GAL3ST3, GAL3ST2"	Galactose-3-O-sulfotransferase 3	GAL3ST3	89792	ENSG00000175229			Gal3st3 (MGI:3617843)			
chr11	66052344	66068910	Chr.11	11q13.1		605591	"SF3B2, SF3B145, SAP145"	"Splicing factor 3B, subunit 2"	SF3B2	10992	ENSG00000087365			Sf3b2 (MGI:2441856)			
chr11	66070275	66244746	11q13.1	11q13.1-q13.2		607492	"PACS1, SHMS, MRD17"	Phosphofurin acidic cluster sorting protein 1	PACS1	55690	ENSG00000175115		"Schuurs-Hoeijmakers syndrome, 615009 (3), Autosomal dominant"	Pacs1 (MGI:1277113)			
chr11	66257293	66267860	11q12-q13	11q13.2		611729	"KLC2, SPOAN"	"Kinesin, light chain 2"	KLC2	64837	ENSG00000174996		"Spastic paraplegia, optic atrophy, and neuropathy, 609541 (3), Autosomal recessive"	Klc2 (MGI:107953)			
chr11	66268525	66277491	11q13.1	11q13.2		612565	RAB1B	Ras-associated protein RAB1B	RAB1B	81876	ENSG00000174903			Rab1b (MGI:1923558)			
chr11	66278200	66284213	11q13.2	11q13.2		611288	"CNIH2, CNIL"	"Cornichon, Drosophila, homolog of, 2"	CNIH2	254263	ENSG00000174871			Cnih2 (MGI:1277225)			
chr11	66284579	66289166	11q13	11q13.2		611484	"YIF1A, YIF1"	"Yip1-interacting factor, S. cerevisiae, homolog of, A"	YIF1A	10897	ENSG00000174851			Yif1a (MGI:1915340)			
chr11	66314486	66317043	11q13	11q13.2		606064	"CD248, TEM1"	CD248 antigen	CD248	57124	ENSG00000174807			Cd248 (MGI:1917695)			
chr11	66337332	66345124	11q13.1-q13.2	11q13.2		606259	BRMS1	Breast cancer metastasis suppressor 1	BRMS1	25855	ENSG00000174744			Brms1 (MGI:2388804)			
chr11	66345371	66347689	11q13.2	11q13.2		605517	"B4GAT1, B3GNT1, IGNT, IGAT, MDDGA13"	"Beta-1,4glucuronyltransferase 1"	B4GAT1	11041	ENSG00000174684		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13, 615287 (3), Autosomal recessive"	B4gat1 (MGI:1919680)			
chr11	66362520	66372475	11q13	11q13.2		602110	"SLC29A2, HNP36, DER12"	"Solute carrier family 29 (nucleoside transporters), member 2 (hydrophobic nucleolar protein, 36kD)"	SLC29A2	3177	ENSG00000174669			Slc29a2 (MGI:1345278)			
chr11	66408921	66426706	11q13	11q13.2		608554	"NPAS4, NXF"	Neuronal PAS domain protein 4	NPAS4	266743	ENSG00000174576			Npas4 (MGI:2664186)			
chr11	66435074	66438859	11q13.3	11q13.2		611826	MRPL11	Mitochondrial ribosomal protein L11	MRPL11	65003	ENSG00000174547			Mrpl11 (MGI:2137215)			
chr11	66466326	66477336	11q13.2	11q13.2		609827	PELI3	"Pellino, Drosophila, homolog of, 3"	PELI3	246330	ENSG00000174516			Peli3 (MGI:1924963)			
chr11	66480012	66509658	11q12-q13.1	11q13.2		606818	DPP3	Dipeptidyl peptidase III	DPP3	10072	ENSG00000254986			Dpp3 (MGI:1922471)			
chr11	66510647	66533612	11q13	11q13.2		209901	BBS1	BBS1 gene	BBS1	582	ENSG00000174483		"Bardet-Biedl syndrome 1, 209900 (3), Autosomal recessive, Digenic recessive"	Bbs1 (MGI:1277215)			
chr11	66546394	66563328	11q13-q14	11q13.2		102574	"ACTN3, ACTN3D"	"Actinin, alpha-3"	ACTN3	89	ENSG00000248746		"[Alpha-actinin-3 deficiency], 617749 (3); [Sprinting performance], 617749 (3)"				
chr11	66563462	66568575	11q13.1	11q13.2		603539	"CTSF, CLN13"	Cathepsin F	CTSF	8722	ENSG00000174080		"Ceroid lipofuscinosis, neuronal, 13, Kufs type, 615362 (3), Autosomal recessive"	Ctsf (MGI:1861434)			
chr11	66593161	66606018	11q13	11q13.2		603864	CCS	Copper chaperone for superoxide dismutase	CCS	9973	ENSG00000173992			Ccs (MGI:1333783)			
chr11	66616581	66629933	11q13	11q13.2		612409	"RBM14, PSP2, COAA, SIP"	RNA-binding motif protein 14	RBM14	10432	ENSG00000239306			Rbm14 (MGI:1929092)			
chr11	66638616	66668384	11q13	11q13.2		602571	RBM4. LARK	"RNA-binding motif protein-4 (lark, Drosophila, homolog of)"	RBM4	5936	ENSG00000173933			Rbm4 (MGI:1100865)			
chr11	66682495	66729360	11q13	11q13.2		604985	"SPTBN2, SCA5, SCAR14"	"Spectrin, beta, nonerythrocytic, 2"	SPTBN2	6712	ENSG00000173898		"Spinocerebellar ataxia 5, 600224 (3), Autosomal dominant; Spinocerebellar ataxia, autosomal recessive 14, 615386 (3), Autosomal recessive"	Sptbn2 (MGI:1313261)			
chr11	66744735	66843515	11q13.2	11q13.2		616109	C11orf80	Chromosome 11 open reading frame 80	C11orf80	79703	ENSG00000173715			Gm960 (MGI:2685806)			
chr11	66843411	66846531	11q13	11q13.2		605385	RCE1	Ras converting CAAX endopeptidase 1	RCE1	9986	ENSG00000173653			Rce1 (MGI:1336895)			
chr11	66848521	66958417	11q13.4-q13.5	11q13.2		608786	PC	Pyruvate carboxylase	PC	5091	ENSG00000173599		"Pyruvate carboxylase deficiency, 266150 (3), Autosomal recessive"	Pcx (MGI:97520)			
chr11	66857086	66860474	11q13.1	11q13.2		612810	"LRFN4, SALM3"	Leucine-rich repeat and fibronectin type III domain-containing protein 4	LRFN4	78999	ENSG00000173621			Lrfn4 (MGI:2385612)			
chr11	67006772	67050862	11q13.2	11q13.2		606436	"SYT12, SRG1"	Synaptotagmin 12	SYT12	91683	ENSG00000173227			Syt12 (MGI:2159601)			
chr11	67056817	67072016	11q14.3	11q13.2		605781	"RHOD, ARHD, RHOHP1"	"Ras homolog gene family, member D"	RHOD	29984	ENSG00000173156			Rhod (MGI:108446)			
chr11	67119268	67258081	Chr.11	11q13.2		605657	"FBXL11, FBL11"	F-box and leucine-rich repeat protein-11	KDM2A	22992	ENSG00000173120			Kdm2a (MGI:1354736)			
chr11	67266399	67286557	11cen-q13	11q13.2		109635	ADRBK1	"Adrenergic, beta, receptor kinase-1"	GRK2	156	ENSG00000173020			Grk2 (MGI:87940)			
chr11	67289290	67302483	11q13.2	11q13.2		615126	ANKRD13D	Ankyrin repeat domain-containing protein 13D	ANKRD13D	338692	ENSG00000172932			Ankrd13d (MGI:1915673)			
chr11	67303447	67312606	11q13.2	11q13.2		606780	SSH3	"Slingshot, Drosophila, homolog of, 3"	SSH3	54961	ENSG00000172830			Ssh3 (MGI:2683546)			
chr11	67350764	67353595	11q13	11q13.2		611525	"POLD4, POLDS, P12"	"Polymerase, DNA-directed, delta 4"	POLD4	57804	ENSG00000175482			Pold4 (MGI:1916995)			
chr11	67364167	67374176	11q13.3	11q13.2		607672	"CLCF1, BSF3, CLC, CISS2"	Cardiotrophin-like cytokine	CLCF1	23529	ENSG00000175505		"Cold-induced sweating syndrome 2, 610313 (3), Autosomal recessive"	Clcf1 (MGI:1930088)			
chr11	67391951	67398411	11q13.1-q13.2	11q13.2		603761	"RAD9A, RAD9"	"RAD9, S. pombe, homolog of"	RAD9A	5883	ENSG00000172613			Rad9a (MGI:1328356)			
chr11	67398180	67401904	11q13	11q13.2		176875	"PPP1CA, PPP1A"	"Protein phosphatase-1, catalytic subunit, alpha isoform"	PPP1CA	5499	ENSG00000172531			Ppp1ca (MGI:103016)			
chr11	67403717	67410089	11q13.1	11q13.2		610831	"TBC1D10C, CARABIN"	"TBC1 domain family, member 10C"	TBC1D10C	374403	ENSG00000175463			Tbc1d10c (MGI:1922072)			
chr11	67415677	67425606	11q13	11q13.2		613368	"CARNS1, ATPGD1, KIAA1394"	Carnosine synthase 1	CARNS1	57571	ENSG00000172508			Carns1 (MGI:2147595)			
chr11	67435509	67437681	11q13.3	11q13.2		601577	"PTPRCAP, LPAP"	"Protein tyrosine phosphatase, receptor type, c polypeptide-associated protein"	PTPRCAP	5790	ENSG00000213402			Ptprcap (MGI:97811)			
chr11	67438046	67443820	11q13.2	11q13.2		609849	CORO1B	Coronin 1B	CORO1B	57175	ENSG00000172725			Coro1b (MGI:1345963)			
chr11	67452405	67461773	11q13.1	11q13.2		608965	"CABP4, CRSD, CSNB2B"	Calcium-binding protein 4	CABP4	57010	ENSG00000175544		"Cone-rod synaptic disorder, congenital nonprogressive, 610427 (3), Autosomal recessive"	Cabp4 (MGI:1920910)			
chr11	67468178	67491107	11q13.3	11q13.2		605555	"AIP, XAP2, ARA9, PITA1"	Aryl hydrocarbon receptor-interacting protein	AIP	9049	ENSG00000110711		"Pituitary adenoma 1, multiple types, 102200 (3), Autosomal dominant, Somatic mutation; Pituitary adenoma predisposition, 102000 (3), Autosomal dominant"	Aip (MGI:109622)			
chr11	67518946	67523427	11q13.1	11q13.2		607314	"CABP2, DFNB93"	Calcium-binding protein 2	CABP2	51475	ENSG00000167791		"Deafness, autosomal recessive 93, 614899 (3), Autosomal recessive"	Cabp2 (MGI:1352749)			
chr11	67583594	67586652	11q13	11q13.2		134660	"GSTP1, GST3"	Glutathione S-transferase pi	GSTP1	2950	ENSG00000084207	formerly called GST1		"Gstp2,Gstp-ps,Gstp1 (MGI:95865,MGI:3782108,MGI:95864)"			
chr11	67606851	67612540	11q13	11q13.2		161015	"NDUFV1, UQOR1"	"NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kD"	NDUFV1	4723	ENSG00000167792		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufv1 (MGI:107851)			
chr11	67631302	67639559	11q13.1-q13.2	11q13.2		604648	TBX10	T-box 10	TBX10	347853	ENSG00000167800			Tbx10 (MGI:1261436)			
chr11	67642550	67650828	11q13.2	11q13.2		614413	"ACY3, HCBP1"	Aminoacylase 3	ACY3	91703	ENSG00000132744			Acy3 (MGI:1918920)			
chr11	67662161	67681223	Chr.11	11q13.2		601917	"ALDH3B2, ALDH8"	"Aldehyde dehydrogenase 3 family, member B2"	ALDH3B2	222	ENSG00000132746						
chr11	67991099	68004124	11q13	11q13.2		608204	"UNC93B1, IIAE1"	"UNC93, C. elegans, homolog of, B1"	UNC93B1	81622	ENSG00000110057		"{Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 1}, 610551 (3)"	Unc93b1 (MGI:1859307)			
chr11	68008546	68029281	Chr.11	11q13.2		600466	"ALDH3B1, ALDH7"	"Aldehyde dehydrogenase 3 family, member B1"	ALDH3B1	221	ENSG00000006534			Aldh3b1 (MGI:1914939)			
chr11	68030616	68036646	11q13	11q13.2		602141	NDUFS8	"NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kD (NADH-coenzyme Q reductase)"	NDUFS8	4728	ENSG00000110717	previously assigned to 3q28	"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufs8 (MGI:2385079)			
chr11	68038994	68053845	11q13.4-q13.5	11q13.2		604592	"TCIRG1, TIRC7, OC116, OPTB1"	T-cell immune regulator 1	TCIRG1	10312	ENSG00000110719		"Osteopetrosis, autosomal recessive 1, 259700 (3), Autosomal recessive"	Tcirg1 (MGI:1350931)			
chr11	68052858	68121390	11q13.2	11q13.2		118491	"CHKA, CHK"	"Choline kinase, alpha"	CHKA	1119	ENSG00000110721			Chka (MGI:107760)			
chr11	68154862	68213898	11q13	11q13.2		610881	"KMT5B, SUV420H1, CGI85, MRD51"	Lysine methyltransferase 5B	KMT5B	51111	ENSG00000110066		"Mental retardation, autosomal dominant 51, 617788 (3), Autosomal dominant"	Kmt5b (MGI:2444557)			
chr11	68261334	68272000	11q13	11q13.2		610880	C11orf24	Chromosome 11 open reading frame 24	C11orf24	53838	ENSG00000171067			1810055G02Rik (MGI:1919306)			
chr11	68298865	68449274	11q13.4	11q13.2		603506	"LRP5, BMND1, LRP7, LR3, OPPG, VBCH2, OPTA1, EVR4, PCLD4"	Low density lipoprotein receptor-related protein-5	LRP5	4041	ENSG00000162337		"[Bone mineral density variability 1], 601884 (3), Autosomal dominant; Exudative vitreoretinopathy 4, 601813 (3), Autosomal recessive, Autosomal dominant; Hyperostosis, endosteal, 144750 (3), Autosomal dominant; Osteopetrosis, autosomal dominant 1, 607634 (3), Autosomal dominant; Osteoporosis-pseudoglioma syndrome, 259770 (3), Autosomal recessive; {Osteoporosis}, 166710 (3), Autosomal dominant; Osteosclerosis, 144750 (3), Autosomal dominant; Polycystic liver disease 4 with or without kidney cysts, 617875 (3), Autosomal dominant; van Buchem disease, type 2, 607636 (3), Autosomal dominant"	Lrp5 (MGI:1278315)			
chr11	68460717	68615333	11q13	11q13.2		610879	"SAPS3, PP6R3, C11orf23, KIAA1558"	"SAPS domain family, member 3"	PPP6R3	55291	ENSG00000110075			Ppp6r3 (MGI:1921807)			
chr11	68684474	68691174	11q13.3-q13.5	11q13.2		137035	"GAL, GALN, GLNN, ETL8"	Galanin	GAL	51083	ENSG00000069482	mutation identified in 1 ETL8 family	"?Epilepsy, familial temporal lobe, 8, 616461 (3), Autosomal dominant"	Gal (MGI:95637)			
chr11	68700000	75500000	11q13.3-q13.4			194633	ZNF126	Zinc finger protein-126 (HZF-2)									
chr11	68706673	68751563	11q13.2-q13.3	11q13.3		604374	"MTL5, TESMIN"	"Metallothionein-like 5, testis-specific"	TESMIN	9633	ENSG00000132749			Tesmin (MGI:1340029)			
chr11	68754619	68844409	11q13	11q13.3		600528	CPT1A	"Carnitine palmitoyltransferase I, liver"	CPT1A	1374	ENSG00000110090		"CPT deficiency, hepatic, type IA, 255120 (3), Autosomal recessive"	Cpt1a (MGI:1098296)			
chr11	68891275	68903834	11q13.2	11q13.3		611834	MRPL21	Mitochondrial ribosomal protein L21	MRPL21	219927	ENSG00000197345			Mrpl21 (MGI:2660674)			
chr11	68903850	68940600	11q13.2-q13.4	11q13.3		600502	"IGHMBP2, SMUBP2, CATF1, SMARD1, HMN6, CMT2S"	Immunoglobulin mu binding protein 2	IGHMBP2	3508	ENSG00000132740		"Charcot-Marie-Tooth disease, axonal, type 2S, 616155 (3), Autosomal recessive; Neuronopathy, distal hereditary motor, type VI, 604320 (3), Autosomal recessive"	Ighmbp2 (MGI:99954)			
chr11	68980020	68980985	11q13.2	11q13.3		607231	"MRGPRD, MRGD"	"Mas-related G protein-coupled receptor family, member D"	MRGPRD	116512	ENSG00000172938			Mrgprd (MGI:3033142)			
chr11	69004374	69013670	11q13.2	11q13.3		607233	"MRGPRF, MRGF, RTA"	"Mas-related G protein-coupled receptor family, member F"	MRGPRF	116535	ENSG00000172935			Mrgprf (MGI:2384823)			
chr11	69048875	69090603	11q13.2	11q13.3		612163	"TPCN2, TPC2, SHEP10"	Two-pore segment channel 2	TPCN2	219931	ENSG00000162341		"[Skin/hair/eye pigmentation 10, blond/brown hair], 612267 (3)"	Tpcn2 (MGI:2385297)			
chr11	69294137	69297286	11q13.1	11q13.3		605625	MYEOV	Myeloma overexpressed gene	MYEOV	26579	ENSG00000172927						
chr11	69485560	69493542	11q13	11q13.3		617696	"CUPID1, LINC01488, BRCAT8"	"CCND1 upstream intergenic DNA repair 1, noncoding"	LINC01488	101928292							
chr11	69641104	69654473	11q13	11q13.3		168461	"CCND1, PRAD1, BCL1"	Cyclin D1	CCND1	595	ENSG00000110092	pseudogene on 11q13	"{Colorectal cancer, susceptibility to}, 114500 (3), Autosomal dominant; {Multiple myeloma, susceptibility to}, 254500 (3), Somatic mutation; {von Hippel-Lindau syndrome, modifier of}, 193300 (3), Autosomal dominant"	Ccnd1 (MGI:88313)			
chr11	69665562	69675396	11q13	11q13.3		607224	"ORAOV1, TAOS1"	Oral cancer overexpressed gene 1	ORAOV1	220064	ENSG00000149716			Oraov1 (MGI:1919534)			
chr11	69698237	69704337	11q13.1	11q13.3		603891	FGF19	Fibroblast growth factor 19	FGF19	9965	ENSG00000162344			Fgf15 (MGI:1096383)			
chr11	69771015	69775402	11q13	11q13.3		164980	"FGF4, HSTF1"	Fibroblast growth factor-4 (heparin secretory transforming protein-1; Kaposi sarcoma oncogene)	FGF4	2249	ENSG00000075388	coamplified with FGF3 in melanoma		Fgf4 (MGI:95518)			
chr11	69809967	69819423	11q13	11q13.3		164950	"FGF3, INT2"	Fibroblast growth factor-3 (oncogene INT2)	FGF3	2248	ENSG00000186895	35kb 5' to HST1	"Deafness, congenital with inner ear agenesis, microtia, and microdontia, 610706 (3), Autosomal recessive"	Fgf3 (MGI:95517)			
chr11	70078301	70189544	11q13	11q13.3		610108	"ANO1, TMEM16A, FLJ10261"	"Anoctamin 1, calcium activated chloride channel"	ANO1	55107	ENSG00000131620			Ano1 (MGI:2142149)			
chr11	70203162	70207401	11q13.3	11q13.3		602457	FADD	FAS-associating protein with death domain	FADD	8772	ENSG00000168040		"Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations, 613759 (3), Autosomal recessive"	Fadd (MGI:109324)			
chr11	70270686	70384500	11q13.3	11q13.3		611054	"PPFIA1, LIP1"	"Protein-tyrosine phosphatase, receptor-type, F polypeptide-interacting protein alpha-1"	PPFIA1	8500	ENSG00000131626			Ppfia1 (MGI:1924750)			
chr11	70398505	70436583	11q13	11q13.3		164765	"CTTN, EMS1"	Cortactin	CTTN	2017	ENSG00000085733	amplified in breast cancer and squamous cell cancer		Cttn (MGI:99695)			
chr11	70467855	71252723	11q13.3-q13.4	11q13.3-q13.4		603290	"SHANK2, CORTBP1, AUTS17"	SH3 and multiple ankyrin repeat domains 2	SHANK2	22941	ENSG00000162105		"{Autism susceptibility 17}, 613436 (3)"	Shank2 (MGI:2671987)			
chr11	71434410	71448430	11q12-q13	11q13.4		602858	"DHCR7, SLOS"	Delta-7-dehydrocholesterol reductase	DHCR7	1717	ENSG00000172893		"Smith-Lemli-Opitz syndrome, 270400 (3), Autosomal recessive"	Dhcr7 (MGI:1298378)			
chr11	71453170	71501537	11q13.2	11q13.4		608285	NADSYN1	NAD synthetase 1	NADSYN1	55191	ENSG00000172890			Nadsyn1 (MGI:1926164)			
chr11	71548419	71549606	11q13.5	11q13.4		148021	"KRTAP5-9, KRN1"	Keratin associated protein 5-9	KRTAP5-9	3846	ENSG00000254997						
chr11	71787510	71801233	11q13.4	11q13.4		616124	FAM86C1	"Family with sequence similarity 86, member C1"	FAM86C1	55199	ENSG00000158483						
chr11	71997943	72002918	11q13.4	11q13.4		604113	IL18BP	Interleukin 18-binding protein	IL18BP	10068	ENSG00000137496			Il18bp (MGI:1333800)			
chr11	72002863	72080692	11q13	11q13.4		164009	NUMA1	Nuclear mitotic apparatus protein-1	NUMA1	4926	ENSG00000137497	fused with RARA in APL	"Leukemia, acute promyelocytic, somatic, 612376 (3)"	Numa1 (MGI:2443665)			
chr11	72080330	72110781	11q13.3-q13.4	11q13.4		612414	"LRTOMT, LRTOMT1, LRTOMT2, DFNB63"	Leucine-rich transmembrane O-methyltransferase	LRTOMT	220074	ENSG00000284844		"Deafness, autosomal recessive 63, 611451 (3), Autosomal recessive"	Tomt (MGI:3769724)			
chr11	72097291	72103386	11q13.4	11q13.4		613510	"LAMTOR1, C11orf59, PDRO"	"Late endosomal/lysosomal adaptor, mitogen-activated protein kinase and mammalian target of rapamycin activator 1"	LAMTOR1	55004	ENSG00000149357			Lamtor1 (MGI:1913758)			
chr11	72106375	72112779	11q13.4	11q13.4		614717	"ANAPC15, APC15"	"Anaphase-promoting complex, subunit 15"	ANAPC15	25906	ENSG00000110200						
chr11	72135709	72139891	11q13.4	11q13.4		602469	FOLR3	Folate receptor 3	FOLR3	2352	ENSG00000110203						
chr11	72189557	72196322	11q13.3-q13.5	11q13.4		136430	FOLR1	"Folate receptor-1, adult"	FOLR1	2348	ENSG00000110195	telomeric of FGF3	"Neurodegeneration due to cerebral folate transport deficiency, 613068 (3), Autosomal recessive"	Folr1 (MGI:95568)			
chr11	72216772	72221949	11q13.3-q13.5	11q13.4		136425	FOLR2	Folate receptor-2 (fetal)	FOLR2	2350	ENSG00000165457	23kb from FOLR1		Folr2 (MGI:95569)			
chr11	72223860	72239146	11q23	11q13.4		600829	"INPPL1, OPSMD"	Inositol polyphosphate phosphatase-like 1	INPPL1	3636	ENSG00000165458		"Opsismodysplasia, 258480 (3), Autosomal recessive"	Inppl1 (MGI:1333787)			
chr11	72239076	72244175	11q13.3-q13.4	11q13.4		602753	"PHOX2A, ARIX, CFEOM2"	Paired-like (astraless) homeobox 2a	PHOX2A	401	ENSG00000165462		"Fibrosis of extraocular muscles, congenital, 2, 602078 (3), Autosomal recessive"	Phox2a (MGI:106633)			
chr11	72292424	72434683	11q13.4	11q13.4		616254	"CLPB, SKD3, MEGCANN, MGCA7"	Caseinolytic peptidase B	CLPB	81570	ENSG00000162129		"3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 (3), Autosomal recessive"	Clpb (MGI:1100517)			
chr11	72576139	72674452	11q13.4	11q13.4		602658	PDE2A	Phosphodiesterase 2A	PDE2A	5138	ENSG00000186642			Pde2a (MGI:2446107)			
chr11	72615062	72615129	11q13.4	11q13.4		615017	"MIR139, MIR139-3p"	Micro RNA 139	MIR139	406931							
chr11	72685068	72752388	11q13.4	11q13.4		606646	"ARAP1, CENTD2, KIAA0782"	"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1"	ARAP1	116985	ENSG00000186635			Arap1 (MGI:1916960)			
chr11	72754728	72793704	11q13	11q13.4		617382	STARD10	START domain-containing protein 10	STARD10	10809	ENSG00000214530			Stard10 (MGI:1860093)			
chr11	72836742	73142681	11q13.4	11q13.4		617556	"FCHSD2, KIAA0769, NWK"	FCH and double SH3 domains protein 2	FCHSD2	9873	ENSG00000137478			Fchsd2 (MGI:2448475)			
chr11	73200415	73246742	11q13.5	11q13.4		600041	"P2RY2, P2Y2, P2U"	"Purinergic receptor P2Y, G-protein coupled, 2"	P2RY2	5029	ENSG00000175591			P2ry2 (MGI:105107)			
chr11	73264502	73298624	11q13.5	11q13.4		602451	"P2RY6, P2Y6"	"Pyrimidinergic receptor P2Y, G protein-coupled, 6"	P2RY6	5031	ENSG00000171631			P2ry6 (MGI:2673874)			
chr11	73305960	73369379	11q13.4	11q13.4		617043	"ARHGEF17, RHOGEF17, TEM4, KIAA0337"	Rho guanine nucleotide exchange factor 17	ARHGEF17	9828	ENSG00000110237			Arhgef17 (MGI:2673002)			
chr11	73376359	73397473	11q13.4	11q13.4		611211	"RELT, TNFRSF19L"	Receptor expressed in lymphoid tissues	RELT	84957	ENSG00000054967			Relt (MGI:2443373)			
chr11	73400477	73598188	11q13.4	11q13.4		616316	"RAM168A, TCRP1, KIAA0280"	"Family with sequence similarity 168, member A"	FAM168A	23201	ENSG00000054965			Fam168a (MGI:2442372)			
chr11	73646177	73662818	11q13-q14.1	11q13.4		607651	"PLEKHB1, PHR1, KPL1"	"Pleckstrin homology domain-containing protein, family B, member 1"	PLEKHB1	58473	ENSG00000021300			Plekhb1 (MGI:1351469)			
chr11	73675637	73761155	11q13.4	11q13.4		179513	"RAB6A, RAB6"	Oncogene RAB6	RAB6A	5870	ENSG00000175582	previously assigned to 2q14-q21		Rab6a (MGI:894313)			
chr11	73787871	73864610	11q13.2	11q13.4		611853	MRPL48	Mitochondrial ribosomal protein L48	MRPL48	51642	ENSG00000175581	pseudogene on 6		Mrpl48 (MGI:1289321)			
chr11	73870257	73876900	11q13.4	11q13.4		608016	"CHCHD8, E2IG2"	Coiled-coil-helix-coiled-coil-helix domain containing 8	COA4	51287	ENSG00000181924			Coa4 (MGI:1915435)			
chr11	73950318	73970286	11q13.3	11q13.4		610263	"DNAJB13, TSARG6, CILD34"	"DNAJ/HSP40 homolog, subfamily B, member 13"	DNAJB13	374407	ENSG00000187726		"Ciliary dyskinesia, primary, 34, 617091 (3), Autosomal recessive"	Dnajb13 (MGI:1916637)			
chr11	73974670	73982871	11q13	11q13.4		601693	"UCP2, BMIQ4"	Uncoupling protein-2	UCP2	7351	ENSG00000175567		"{Obesity, susceptibility to, BMIQ4}, 607447 (3)"	Ucp2 (MGI:109354)			
chr11	74000280	74009236	11q13	11q13.4		602044	UCP3	Uncoupling protein-3	UCP3	7352	ENSG00000175564		"{Obesity, severe, and type II diabetes}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Ucp3 (MGI:1099787)			
chr11	74012577	74171209	11q13.4	11q13.4		615944	"C2CD3, OFD14"	C2 calcium-dependent domain-containing protein 3	C2CD3	26005	ENSG00000168014	mutation identified in 1 OFD14 patient and 1 OFD14 fetus	"?Orofaciodigital syndrome XIV, 615948 (3), Autosomal recessive"	C2cd3 (MGI:2142166)			
chr11	74171062	74254702	11q13.4	11q13.4		611117	PPME1	Protein phosphatase methylesterase 1	PPME1	51400	ENSG00000214517			Ppme1 (MGI:1919840)			
chr11	74259922	74311675	11q12	11q13.4		608987	P4HA3	"Procollagen-proline, 2-oxoglutarate-4-dioxygenase, alpha subunit, isoform 3"	P4HA3	283208	ENSG00000149380			P4ha3 (MGI:2444049)			
chr11	74330311	74398750	11q13.4	11q13.4		611610	PGM2L1	Phosphoglucomutase 2-like 1	PGM2L1	283209	ENSG00000165434			Pgm2l1 (MGI:1918224)			
chr11	74454840	74467728	11q13-q14	11q13.4		604433	"KCNE3, HOKPP, HYPP"	"Potassium voltage-gated channel, ISK-related subfamily, member 3"	KCNE3	10008	ENSG00000175538		"Brugada syndrome 6, 613119 (3)"	Kcne3 (MGI:1891124)			
chr11	74490510	74493712	11q13.4	11q13.4		617659	LIPT2	Lipoyl(octanoyl) transferase 2	LIPT2	387787	ENSG00000175536		"Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, 617668 (3), Autosomal recessive"	Lipt2 (MGI:1914414)			
chr11	74696427	74731384	11q13.4	11q13.4		613127	"CHRDL2, CHL2, BNF1"	Chordin-like 2	CHRDL2	25884	ENSG00000054938			Chrdl2 (MGI:1916371)			
chr11	74840909	74949186	11q13.3	11q13.4		609788	XRRA1	X-ray radiation resistance-associated 1	XRRA1	143570	ENSG00000166435			Xrra1 (MGI:2181647)			
chr11	74988904	75007697	11q13.5	11q13.4		604617	"NEU3, SIAL3"	Neuraminidase 3 (membrane sialidase; sialidase 3)	NEU3	10825	ENSG00000162139			Neu3 (MGI:1355305)			
chr11	75150986	75206399	Chr.11	11q13.4		604988	"SLC21A9, OATPB"	"Solute carrier family 21 (organic anion transporter), member 9"	SLCO2B1	11309	ENSG00000137491			Slco2b1 (MGI:1351872)			
chr11	75260121	75351830	11q13	11q13.4		107940	ARRB1	"Arrestin, beta 1"	ARRB1	408	ENSG00000137486			Arrb1 (MGI:99473)			
chr11	75335091	75335185	11q13	11q13.4		613755	"MIR326, MIRN326"	Micro RNA 326	MIR326	442900							
chr11	75399490	75422301	11q13.3-q13.5	11q13.4		600454	RPS3	Ribosomal protein S3	RPS3	6188	ENSG00000149273			Rps3 (MGI:1350917)			
chr11	75400390	75400537	11q13.3-q13.5	11q13.4		600455	RNU15A	"RNA, U15a small nucleolar"	SNORD15A	6079		processed from intron of RPS3					
chr11	75434639	75525915	11q13.4-q13.5	11q13.4-q13.5		609632	"GDPD5, GDE2, PP1665"	Glycerophosphodiester phosphodiesterase domain-containing protein 3	GDPD5	81544	ENSG00000158555			Gdpd5 (MGI:2686926)			
chr11	75500000	77400000	11q13.5			613064	ATOD7	"Dermatitis, atopic, 7"		100310755		associated with rs7927894	"{Dermatitis, atopic, susceptibility to, 7}, 613064 (2)"				
chr11	75562055	75572803	11q13.5	11q13.5		600943	"SERPINH1, SERPINH2, PPROM, CBP2, CBP1, OI10"	"Serpin peptidase inhibitor, clade H, member 1"	SERPINH1	871	ENSG00000149257		"Osteogenesis imperfecta, type X, 613848 (3), Autosomal recessive; {Preterm premature rupture of the membranes, susceptibility to}, 610504 (3)"	Serpinh1 (MGI:88283)			
chr11	75586913	75668723	11q13.5	11q13.5		601783	"MAP6, MTAP6, STOP, KIAA1878"	Microtubule-associated protein 6	MAP6	4135	ENSG00000171533			Map6 (MGI:1201690)			
chr11	75717818	75732957	11q13.5	11q13.5		610270	"MOGAT2, MGAT2"	Monoacylglycerol O-acyltransferase 2	MOGAT2	80168	ENSG00000166391			Mogat2 (MGI:2663253)			
chr11	75768732	75801535	11q13.5	11q13.5		606983	DGAT2	Diacylglycerol O-acyltransferase 2	DGAT2	84649	ENSG00000062282			Dgat2 (MGI:1915050)			
chr11	75815166	76144237	11q13	11q13.5		602493	UVRAG	UV radiation resistance-associated gene	UVRAG	7405	ENSG00000198382			Uvrag (MGI:1925860)			
chr11	76186325	76210841	11q13.5	11q13.5		603699	WNT11	"Wingless-type MMTV integration site family, member 11"	WNT11	7481	ENSG00000085741			Wnt11 (MGI:101948)			
chr11	76349955	76380964	11q13.5	11q13.5		607374	PRKRIR	"PRKR inhibitor, repressor of"	THAP12	5612	ENSG00000137492			Thap12 (MGI:1920231)			
chr11	76444927	76553030	11q13.4-q13.5	11q13.5		608574	"EMSY, C11orf30"	EMSY gene	EMSY	56946	ENSG00000158636	100kb from GARP		Emsy (MGI:1924203)			
chr11	76657440	76670940	11q13.5	11q13.5		137207	"LRRC32, GARP, D11S833E"	Leucine rich repeat containing 32	LRRC32	2615	ENSG00000137507			Lrrc32 (MGI:93882)			
chr11	76782312	76798153	11q13.5	11q13.5		608015	"TSKU, E2IG4, TSK"	Tsukushin	TSKU	25987	ENSG00000182704			Tsku (MGI:2443855)			
chr11	76860872	77026796	11q13.5	11q13.5		617036	"ACER3, APHC, PHCA, PLDECO"	Alkaline ceramidase 3	ACER3	55331	ENSG00000078124	mutation identified in 1 PLDECO family	"?Leukodystrophy, progressive, early childhood-onset, 617762 (3), Autosomal recessive"	Acer3 (MGI:1913440)			
chr11	77034340	77041972	11q14	11q13.5		615315	B3GNT6	"Beta-1,3-N-acetylglucosaminyltransferase 6"	B3GNT6	192134	ENSG00000198488			B3gnt6 (MGI:3039603)			
chr11	77066944	77126154	11q14	11q13.5		602537	"CAPN5, HTRA3, VRNI"	Calpain 5	CAPN5	726	ENSG00000149260		"Vitreoretinopathy, neovascular inflammatory, 193235 (3), Autosomal dominant"	Capn5 (MGI:1100859)			
chr11	77102839	77103330	11q13.4-q14.1	11q13.5		164340	OMP	Olfactory marker protein	OMP	4975	ENSG00000254550			Omp (MGI:97436)			
chr11	77128191	77215240	11q13.5	11q13.5		276903	"MYO7A, USH1B, DFNB2, DFNA11"	Myosin VIIA	MYO7A	4647	ENSG00000137474		"Deafness, autosomal dominant 11, 601317 (3), Autosomal dominant; Deafness, autosomal recessive 2, 600060 (3), Autosomal recessive; Usher syndrome, type 1B, 276900 (3), Autosomal recessive"	Myo7a (MGI:104510)			
chr11	77322014	77514956	11q13-q14	11q13.5-q14.1		602590	PAK1	p21/CDC42/RAC1-activated kinase 1	PAK1	5058	ENSG00000149269			Pak1 (MGI:1339975)			
chr11	77400000	93000000	11q14			610888	GCRG224	Gastric cancer-related gene 224		360219							
chr11	77400000	110600000	11q14-q22			612017	IHPS3	"Pyloric stenosis, infantile hypertrophic, 3"		100188876		max lod at rs541821	"Pyloric stenosis, infantile hypertrophic, 3, 612017 (2)"				
chr11	77400000	97400000	11q14-q21			603342	SCZD2	"Schizophrenia susceptibility locus, chromosome 11-related"	SCZD2	6378			"{?Schizophrenia}, 181500 (2), Autosomal dominant"				
chr11	77400000	93000000	11q14			607279	SLEH1	"Systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1"	SLEH1	170682			"{Systemic lupus erythematosus with hemolytic anemia}, 607279 (2)"				
chr11	77589629	77610355	11q14	11q14.1		609914	"AQP11, AQPX1"	Aquaporin 11	AQP11	282679	ENSG00000178301			Aqp11 (MGI:1913583)			
chr11	77616150	77637805	11q13.5-q14.1	11q14.1		602158	"CLNS1A, CLNS1B"	"Chloride channel, nucleotide-sensitive, 1A"	CLNS1A	1207	ENSG00000074201	CLNS1B on 6p12.1-q13 = pseudogene?		Clns1a (MGI:109638)			
chr11	77660008	77872231	11q13	11q14.1		608522	"HBXAP, RSF1"	Hepatitis B virus X-associated protein	RSF1	51773	ENSG00000048649			Rsf1 (MGI:2682305)			
chr11	77874417	77994670	11q14.1	11q14.1		611348	"INTS4, INT4"	Integrator complex subunit 4	INTS4	92105	ENSG00000149262			Ints4 (MGI:1917164)			
chr11	78063860	78068356	11q13.5	11q14.1		601926	THRSP	"Thyroid hormone responsive SPOT14, rat, homolog of"	THRSP	7069	ENSG00000151365			Thrsp (MGI:109126)			
chr11	78068346	78080218	11q14.1	11q14.1		603845	NDUFC2	"NADH-ubiquinone oxidoreductase 1, subunit C2"	NDUFC2	4718	ENSG00000151366			Ndufc2 (MGI:1344370)			
chr11	78100941	78139652	11pter-p15.5	11q14.1		608103	"ALG8, CDG1H, PCLD3"	"Alg8, S. cerevisiae, homolog of"	ALG8	79053	ENSG00000159063		"Congenital disorder of glycosylation, type Ih, 608104 (3), Autosomal recessive; Polycystic liver disease 3 with or without kidney cysts, 617874 (3)"	Alg8 (MGI:2141959)			
chr11	78215289	78417821	11q13.4-q13.5	11q14.1		606203	GAB2	GRB2-associated binding protein 2	GAB2	9846	ENSG00000033327			Gab2 (MGI:1333854)			
chr11	78435960	78574863	11q14.1	11q14.1		612803	"NARS2, COXPD24"	Asparaginyl-tRNA synthetase 2	NARS2	79731	ENSG00000137513		"Combined oxidative phosphorylation deficiency 24, 616239 (3), Autosomal recessive"	Nars2 (MGI:2142075)			
chr11	78653282	79441018	11q14.1	11q14.1		610084	"TENM4, ODZ4, TNM4, DOC4, KIAA1302, ETM5"	Teneurin transmembrane protein 4	TENM4	26011	ENSG00000149256		"Essential tremor, hereditary, 5, 616736 (3), Autosomal dominant"	Tenm4 (MGI:2447063)			
chr11	82822939	82901739	11q14	11q14.1		176785	"PRCP, PCP"	Prolylcarboxypeptidase (angiotensinase C)	PRCP	5547	ENSG00000137509			Prcp (MGI:1919711)			
chr11	82973132	83071922	11q12-q14	11q14.1		605693	RAB30	Ras-associated protein RAB30	RAB30	27314	ENSG00000137502			Rab30 (MGI:1923235)			
chr11	83157094	83185793	11q14.1	11q14.1		608876	"PCF11, KIAA0824"	"PCF11, yeast, homolog of"	PCF11	51585	ENSG00000165494			Pcf11 (MGI:1919579)			
chr11	83455008	85628534	11q21	11q14.1		603583	DLG2	"Discs large, Drosophila, homolog of, 2 (channel-associated protein of synapses, 110kD)"	DLG2	1740	ENSG00000150672			Dlg2 (MGI:1344351)			
chr11	85628572	85636539	11q14.1	11q14.1		615533	TMEM126B	Transmembrane protein 126B	TMEM126B	55863	ENSG00000171204		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Tmem126b (MGI:1915722)			
chr11	85647918	85656552	11q14.1-q21	11q14.1		612988	"TMEM126A, OPA7"	Transmembrane protein 126A	TMEM126A	84233	ENSG00000171202		"Optic atrophy 7, 612989 (3), Autosomal recessive"	Tmem126a (MGI:1913521)			
chr11	85694220	85811181	11q14	11q14.1		612880	"SYTL2, SLP2, SLP2A, EXO4, KIAA1597"	Synaptotagmin-like 2	SYTL2	54843	ENSG00000137501			Sytl2 (MGI:1933366)			
chr11	85957170	86069880	11q14	11q14.2		603025	"PICALM, CALM, CLTH, LAP"	Phosphatidylinositol-binding clathrin assembly protein	PICALM	8301	ENSG00000073921	fuses with AF10 in t(10;11)	"Leukemia, acute myeloid, somatic, 601626 (3)"	Picalm (MGI:2385902)			
chr11	86244383	86285419	11q14.2-q22.3	11q14.2		605984	"EED, WAIT1, COGIS"	"Embryonic ectoderm development protein, mouse, homolog of"	EED	8726	ENSG00000074266		"Cohen-Gibson syndrome, 617561 (3), Autosomal dominant"	Eed (MGI:95286)			
chr11	86302210	86345942	11q14.2	11q14.2		614908	"HIKESHI, C11orf73, HLD13"	Hikeshi	HIKESHI	51501	ENSG00000149196		"Leukodystrophy, hypomyelinating, 13, 616881 (3), Autosomal recessive"	Hikeshi (MGI:96738)			
chr11	86441107	86674745	11cen-q22.3	11q14.2		604626	ME3	Malic enzyme 3	ME3	10873	ENSG00000151376			Me3 (MGI:1916679)			
chr11	86945674	86955397	11q14-q21	11q14.2		604579	"FZD4, EVR1"	"Frizzled, Drosophila, homolog of, 4"	FZD4	8322	ENSG00000174804		"Exudative vitreoretinopathy 1, 133780 (3), Autosomal dominant; Retinopathy of prematurity, 133780 (3), Autosomal dominant"	Fzd4 (MGI:108520)			
chr11	87037843	87328833	11q14.2	11q14.2		616360	"TMEM135, PMP52"	Transmembrane protein 135	TMEM135	65084	ENSG00000166575			Tmem135 (MGI:1920009)			
chr11	87809489	88175503	11q13.5-q22.3	11q14.2		606281	RAB38	"Ras-family, member RAB38"	RAB38	23682	ENSG00000123892			Rab38 (MGI:1919683)			
chr11	88293591	88337786	11q14.1-q14.3	11q14.2		602365	"CTSC, CPPI, PALS, PLS, HMS, PDON1, JPD"	Cathepsin C	CTSC	1075	ENSG00000109861		"Haim-Munk syndrome, 245010 (3), Autosomal recessive; Papillon-Lefevre syndrome, 245000 (3), Autosomal recessive; Periodontitis 1, juvenile, 170650 (3), Autosomal recessive"	Ctsc (MGI:109553)			
chr11	88504575	89065962	11q14.2-q14.3	11q14.2-q14.3		604102	"GRM5, MGLUR5"	"Glutamate receptor, metabotropic, 5"	GRM5	2915	ENSG00000168959			Grm5 (MGI:1351342)			
chr11	89177564	89295758	11q14-q21	11q14.3		606933	"TYR, SHEP3, CMM8, OCA1A, ATN"	Tyrosinase	TYR	7299	ENSG00000077498		"Albinism, oculocutaneous, type IA, 203100 (3), Autosomal recessive; Albinism, oculocutaneous, type IB, 606952 (3); {Melanoma, cutaneous malignant, susceptibility to, 8}, 601800 (3); [Skin/hair/eye pigmentation 3, blue/green eyes], 601800 (3); [Skin/hair/eye pigmentation 3, light/dark/freckling skin], 601800 (3); Waardenburg syndrome/albinism, digenic, 103470 (3), Autosomal dominant"	Tyr (MGI:98880)			
chr11	89324352	89589610	11q14.2-q21	11q14.3		605261	"NOX4, RENOX"	NADPH oxidase 4	NOX4	50507	ENSG00000086991			Nox4 (MGI:1354184)			
chr11	89637579	89698717	11p13-p11.1	11q14.3		609020	"FOLH1B, PSMAL, GCP3"	Folate hydrolase 1B	FOLH1B	219595							
chr11	89766435	89808574	11p11.12-q12	11q14.3		606124	RNF18	RING finger protein-18	TRIM49	57093	ENSG00000168930						
chr11	90085949	90087130	11q14.3	11q14.3		613696	"UBTFL1, HMGPI"	Upstream binding transcription factor (RNA polymerase I)-like 1	UBTFL1	642623	ENSG00000255009						
chr11	90131692	90193576	11q14.3-q21	11q14.3		611636	NAALAD2	N-acetylated alpha-linked acidic dipeptidase 2	NAALAD2	10003	ENSG00000077616			Naalad2 (MGI:1919810)			
chr11	92224635	92896472	11q14.3-q21	11q14.3		612483	FAT3	"FAT tumor suppressor, Drosophila, homolog of, 3"	FAT3	120114	ENSG00000165323			Fat3 (MGI:2444314)			
chr11	92969622	92986240	11q21-q22	11q14.3		600804	MTNR1B	Melatonin receptor 1B	MTNR1B	4544	ENSG00000134640		"{Diabetes mellitus, type 2, susceptibility to}, 125853 (3), Autosomal dominant"	Mtnr1b (MGI:2181726)			
chr11	93000000	110600000	11q21-q22			613233	FGQTL3	Fasting plasma glucose level QTL 3		100379217		associated with rs10830963	"[Fasting plasma glucose level QTL 3], 613233 (2)"				
chr11	93144170	93386037	11q14.3	11q21		613760	"SLC36A4, PAT4"	"Solute carrier family 36, member 4"	SLC36A4	120103	ENSG00000180773			Slc36a4 (MGI:2442595)			
chr11	93329078	93438469	11q21	11q21		617148	"DEUP1, CCDC67"	Deuterosome assembly protein 1	DEUP1	159989	ENSG00000165325			Deup1 (MGI:2443026)			
chr11	93478471	93553978	11q21	11q21		609477	"C11orf75, FN5"	"FN5, pufferfish, homolog of"	SMCO4	56935	ENSG00000166002						
chr11	93661649	93730380	11q21	11q21		617728	"CEP295, KIAA1731"	"Centrosomal protein, 295kD"	CEP295	85459	ENSG00000166004			Cep295 (MGI:2442521)			
chr11	93730193	93741536	11q21	11q21		612823	"TAF1D, RAFI41, JOSD3"	TATA box-binding protein-associated factor 1D	TAF1D	79101	ENSG00000166012			Taf1d (MGI:1922566)			
chr11	93741593	93763101	11q21	11q21		615810	"C11orf54, PTOD012"	Chromosome 11 open reading frame 54	C11orf54	28970	ENSG00000182919			4931406C07Rik (MGI:1918234)			
chr11	93784238	93813329	11q21	11q21		603810	"MED17, CRSP6, CRSP77, TRAP80, DRIP80"	Mediator complex subunit 17	MED17	9440	ENSG00000042429		"Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3), Autosomal recessive"	Med17 (MGI:2182585)			
chr11	94128927	94185595	11q21	11q21		608420	"PANX1, PX1"	Pannexin 1	PANX1	24145	ENSG00000110218			Panx1 (MGI:1860055)			
chr11	94305636	94307691	11q21	11q21		615737	FOLR4	Folate receptor 4	IZUMO1R	390243	ENSG00000183560			Izumo1r (MGI:1929185)			
chr11	94377310	94401422	11q21	11q21		605569	"GPR83, GIR, GPR72"	G protein-coupled receptor 83	GPR83	10888	ENSG00000123901			Gpr83 (MGI:95712)			
chr11	94415569	94512700	11q21	11q21		600814	"MRE11A, MRE11, ATLD"	"Meiotic recombination 11, S. cerevisiae, homolog A of"	MRE11	4361	ENSG00000020922		"Ataxia-telangiectasia-like disorder 1, 604391 (3), Autosomal recessive"	Mre11a (MGI:1100512)			
chr11	94543850	94549897	11q21	11q21		104230	"FUT4, FCT3A, CD15"	"Fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific)"	FUT4	2526	ENSG00000196371			Fut4 (MGI:95594)			
chr11	94567307	94621420	11q12	11q21		610315	"PIWIL4, HIWI2, MIWI2"	PIWI-like 4	PIWIL4	143689	ENSG00000134627			Piwil4 (MGI:3041167)			
chr11	94706417	94876752	11q21	11q21		614657	"AMOTL1, JEAP"	Angiomotin-like 1	AMOTL1	154810	ENSG00000166025			Amotl1 (MGI:1922973)			
chr11	94973680	94999513	11q21	11q21		609766	JMJD2D	Jumonji domain-containing protein 2D	KDM4D	55693	ENSG00000186280			Kdm4d (MGI:3606484)			
chr11	95025257	95027595	11q21	11q21		616581	"KDM4E, JMJD2E"	Lysine-specific demethylase 4E	KDM4E	390245	ENSG00000235268						
chr11	95066876	95071226	11q22	11q21		603269	"SRSF8, SFRS2B, SRp46"	"Splicing factor, arginine/serine-rich, 8"	SRSF8	10929	ENSG00000263465						
chr11	95165512	95232540	11q21	11q21		607768	SEST3	Sestrin 3	SESN3	143686	ENSG00000149212			Sesn3 (MGI:1922997)			
chr11	95790460	95832692	11q21	11q21		607951	"CEP57, PIG8, TSP57, KIAA0092, MVA2"	Centrosomal protein 57kD	CEP57	9702	ENSG00000166037		"Mosaic variegated aneuploidy syndrome 2, 614114 (3), Autosomal recessive"	Cep57 (MGI:1915551)			
chr11	95832879	95924206	11q22	11q21		603557	"MTMR2, CMT4B1"	Myotubularin-related protein 2	MTMR2	8898	ENSG00000087053		"Charcot-Marie-Tooth disease, type 4B1, 601382 (3), Autosomal recessive"	Mtmr2 (MGI:1924366)			
chr11	95976592	96343307	11q21	11q21		607537	"MAML2, MAM3"	Mastermind-like 2	MAML2	84441	ENSG00000184384	t(11;19)	Mucoepidermoid salivary gland carcinoma (3)				
chr11	96341437	96341525	11q21	11q21		615372	MIR1260B	Micro RNA 1260B	MIR1260B	100422991							
chr11	96389993	96393562	11q21	11q21		603211	"JRKL, HHMJG"	"Jerky, mouse, homolog-like"	JRKL	8690	ENSG00000183340			Jrkl (MGI:1924782)			
chr11	97400000	135086622	11q22-qter			105580	ANC	Anal canal carcinoma		8066		3p22 also deleted	"?Anal canal carcinoma, 105580 (2), Autosomal dominant"				
chr11	99020903	100358884	11q21-q22.2	11q22.1		607219	"CNTN5, NB2"	Contactin 5	CNTN5	53942	ENSG00000149972			Cntn5 (MGI:3042287)			
chr11	100687239	100993944	11q22.1	11q22.1		615936	"ARHGAP42, GRAF3"	Rho GTPase-activating protein 42	ARHGAP42	143872	ENSG00000165895			Arhgap42 (MGI:1918794)			
chr11	101029623	101130680	11q22	11q22.1		607311	PGR	Progesterone receptor	PGR	5241	ENSG00000082175	11q13 = earlier regionalization	"?Progesterone resistance, 264080 (2), Autosomal recessive"	Pgr (MGI:97567)			
chr11	101451469	101583927	11q21-q22	11q22.1		603652	"TRPC6, TRP6, FSGS2"	Transient receptor potential channel-6	TRPC6	7225	ENSG00000137672		"Glomerulosclerosis, focal segmental, 2, 603965 (3)"	Trpc6 (MGI:109523)			
chr11	101890673	101917049	11q22	11q22.1		607666	ANGPTL5	Angiopoietin-like 5	ANGPTL5	253935	ENSG00000187151						
chr11	101915014	102001064	11q22.1	11q22.1		614634	KIAA1377	KIAA1377 gene	CEP126	57562	ENSG00000110318			Cep126 (MGI:2680221)			
chr11	102109956	102233422	11q13	11q22.1		606608	"YAP1, COB1"	"Yes-associated protein 1, 65kD"	YAP1	10413	ENSG00000137693		"Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation, 120433 (3), Autosomal dominant"	Yap1 (MGI:103262)			
chr11	102317372	102339402	11q22-q23	11q22.2		601721	"API2, HAIP1"	Apoptosis inhibitor-2	BIRC3	330	ENSG00000023445	fused with MALT1 in MALT lymphoma		Birc3 (MGI:1197007)			
chr11	102347181	102378669	11q22-q23	11q22.2		601712	"API1, HIAP2"	Apoptosis inhibitor-1	BIRC2	329	ENSG00000110330			Birc2 (MGI:1197009)			
chr11	102396324	102453043	11q22.1	11q22.2		606356	"TMEM123, PORIMIN"	Transmembrane protein 123	TMEM123	114908	ENSG00000152558			Tmem123 (MGI:1919179)			
chr11	102520507	102530752	11q21-q22	11q22.2		178990	MMP7	"Matrix metalloproteinase 7 (matrilysin, uterine)"	MMP7	4316	ENSG00000137673			Mmp7 (MGI:103189)			
chr11	102576834	102625331	11q22.3-q23	11q22.2		604629	"MMP20, AI2A2"	Matrix metalloproteinase-20 (enamelysin)	MMP20	9313	ENSG00000137674		"Amelogenesis imperfecta, type IIA2, 612529 (3), Autosomal recessive"	Mmp20 (MGI:1353466)			
chr11	102711794	102724966	11q21-q22	11q22.2		120355	"MMP8, CLG1"	Matrix metalloproteinase 8 (neutrophil collagenase)	MMP8	4317	ENSG00000118113			Mmp8 (MGI:1202395)			
chr11	102770501	102780627	11q22.3-q23	11q22.2		185260	"MMP10, STMY2"	Matrix metalloproteinase 10 (stromelysin 2)	MMP10	4319	ENSG00000166670			Mmp10 (MGI:97007)			
chr11	102789909	102798234	11q22-q23	11q22.2		120353	"MMP1, CLG"	Matrix metalloproteinase 1 (interstitial collagenase)	MMP1	4312	ENSG00000196611		"COPD, rate of decline of lung function in, 606963 (3); {Epidermolysis bullosa dystrophica, autosomal recessive, modifier of}, 226600 (3), Autosomal recessive"	Mmp1a (MGI:1933846)			
chr11	102835796	102843688	11q23	11q22.2		185250	"MMP3, STMY1, CHDS6"	"Matrix metalloproteinase 3 (stromelysin 1, progelatinase)"	MMP3	4314	ENSG00000149968		"{Coronary heart disease, susceptibility to, 6}, 614466 (3)"	Mmp3 (MGI:97010)			
chr11	102862728	102875033	11q22.2-q22.3	11q22.2		601046	MMP12	Matrix metalloproteinase 12 (macrophage elastase)	MMP12	4321	ENSG00000262406			Mmp12 (MGI:97005)			
chr11	102942991	102955733	11q22.3	11q22.2		600108	"MMP13, CLG3, MANDP1, MDST"	Matrix metalloproteinase 13 (collagenase 3)	MMP13	4322	ENSG00000137745		"Metaphyseal anadysplasia 1, 602111 (3), Autosomal dominant; Metaphyseal dysplasia, Spahr type, 250400 (3), Autosomal recessive; Spondyloepimetaphyseal dysplasia, Missouri type, 602111 (3), Autosomal dominant"	Mmp13 (MGI:1340026)			
chr11	103050683	103092214	11q22.3	11q22.3		616522	"DCUN1D5, SCCRO5"	DCN1 domain-containing protein 5	DCUN1D5	84259	ENSG00000137692			Dcun1d5 (MGI:1924113)			
chr11	103109430	103479862	11q22.3	11q22.3		603297	"DYNC2H1, DNCH2, DHC2, ATD3, SRPS2B, SRTD3"	"Dynein, cytoplasmic-2, heavy chain-1"	DYNC2H1	79659	ENSG00000187240	1 patient showed heterozygous NEK2 and DYNC2H1 mutations	"Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 (3), Autosomal recessive, Digenic recessive"	Dync2h1 (MGI:107736)			
chr11	103907185	104164298	11q22.3	11q22.3		609673	"PDGFD, SCDGFB, IEGF"	Platelet-derived growth factor D	PDGFD	80310	ENSG00000170962			Pdgfd (MGI:1919035)			
chr11	104885717	104898669	11q22.3	11q22.3		608633	"CASP12, CASP12P1"	"Caspase 12, apoptosis-related cysteine protease"	CASP12	100506742	ENSG00000204403		"{Sepsis, susceptibility to} (3)"				
chr11	104942865	104968597	11q22.2-q22.3	11q22.3		602664	CASP4	"Caspase 4, apoptosis-related cysteine protease"	CASP4	837	ENSG00000196954			Casp4 (MGI:107700)			
chr11	104994234	105023901	11q22.2-q22.3	11q22.3		602665	CASP5	"Caspase 5, apoptosis-related cysteine protease"	CASP5	838	ENSG00000137757						
chr11	105025507	105035590	11q22.2-q22.3	11q22.3		147678	"CASP1, IL1BC"	"Caspase 1, apoptosis-related cysteine protease (interleukin-1, beta convertase)"	CASP1	834	ENSG00000137752			Casp1 (MGI:96544)			
chr11	105040217	105045415	11q22	11q22.3		615680	"CARD16, COP1"	Caspase recruitment domain-containing protein 16	CARD16	114769	ENSG00000204397						
chr11	105080452	105101491	11q22	11q22.3		609490	INCA	Inhibitory caspase recruitment domain protein	CARD17	440068	ENSG00000255221						
chr11	105137720	105139733	11q22.3	11q22.3		605354	"CARD18, ICEBERG"	Caspase recruitment domain-containing protein 18	CARD18	59082	ENSG00000255501						
chr11	105609539	105982091	11q22-q23	11q22.3		138246	"GRIA4, GLUR4, NEDSGA"	"Glutamate receptor, ionotropic, AMPA 4"	GRIA4	2893	ENSG00000152578		"Neurodevelopmental disorder with or without seizures and gait abnormalities, 617864 (3), Autosomal dominant"	Gria4 (MGI:95811)			
chr11	106077564	106098691	11q22.3	11q22.3		607756	AASDHPPT	Alpha-aminoadipate semialdehyde dehydrogenase-phosphopantetheinyl transferase	AASDHPPT	60496	ENSG00000149313			Aasdhppt (MGI:1914868)			
chr11	106674011	107018444	11q21-q22	11q22.3		601244	"GUCY1A2, GUC1A2"	"Guanylate cyclase 1, soluble, alpha 2"	GUCY1A2	2977	ENSG00000152402			Gucy1a2 (MGI:2660877)			
chr11	107502725	107565739	11q22.3	11q22.3		613306	"ALKBH8, ABH8"	"AlkB, E. coli, homolog of, 8"	ALKBH8	91801	ENSG00000137760			Alkbh8 (MGI:1914917)			
chr11	107591008	107666778	11q22.3	11q22.3		615456	ELMOD1	ELMO/CED12 domain-containing protein 1	ELMOD1	55531	ENSG00000110675			Elmod1 (MGI:3583900)			
chr11	107707374	107712060	11q22-q23	11q22.3		602203	SLN	Sarcolipin	SLN	6588	ENSG00000170290						
chr11	108008732	108107775	11q22-q23	11q22.3		601741	"CUL5, VACM1"	Cullin-5 (vasopressin-activated calcium-mobilizing receptor-1)	CUL5	8065	ENSG00000166266			Cul5 (MGI:1922967)			
chr11	108116704	108148821	11q22.3-q23.1	11q22.3		607809	ACAT1	Acetyl-Coenzyme A acetyltransferase-1 (acetoacetyl Coenzyme A thiolase)	ACAT1	38	ENSG00000075239	cluster: cen-STMY2-CLG-STMY1-ter	"Alpha-methylacetoacetic aciduria, 203750 (3), Autosomal recessive"	Acat1 (MGI:87870)			
chr11	108155279	108222637	11q22.3	11q22.3		601448	"NPAT, E14"	"Nuclear protein, ataxia-telangiectasia locus"	NPAT	4863	ENSG00000149308			Npat (MGI:107605)			
chr11	108222483	108369098	11q22.3	11q22.3		607585	"ATM, ATA, AT1"	"Ataxia-telangiectasia mutated (includes complementation groups A, C, D, and E)"	ATM	472	ENSG00000149311		"Ataxia-telangiectasia, 208900 (3), Autosomal recessive; {Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant; Lymphoma, B-cell non-Hodgkin, somatic (3); Lymphoma, mantle cell, somatic (3); T-cell prolymphocytic leukemia, somatic (3)"	Atm (MGI:107202)			
chr11	108505430	108607513	11q22.3	11q22.3		612878	"EXPH5, SLAC2B, KIAA0624"	Exophilin 5	EXPH5	23086	ENSG00000110723		"Epidermolysis bullosa, nonspecific, autosomal recessive, 615028 (3), Autosomal recessive"	Exph5 (MGI:2443248)			
chr11	108665024	108940929	11q22-q23	11q22.3		601235	DDX10	DEAD/H box-10 (RNA helicase)	DDX10	1662	ENSG00000178105	400kb telomeric to ATM; pseudogene on 9q21-q22; fused with NUP98 in AML		Ddx10 (MGI:1924841)			
chr11	110092424	110171840	11q22.3	11q22.3		615001	"ZC3H12C, MCPIP3"	Zinc finger CCCH domain-containing protein 12C	ZC3H12C	85463	ENSG00000149289			Zc3h12c (MGI:3026959)			
chr11	110174879	110296711	11q23	11q22.3		179410	"RDX, DFNB24"	Radixin	RDX	5962	ENSG00000137710		"Deafness, autosomal recessive 24, 611022 (3), Autosomal recessive"	Rdx (MGI:97887)			
chr11	110429936	110464883	11q22	11q22.3		103260	"FDX1, ADX"	Ferredoxin-1 (adrenodoxin)	FDX1	2230	ENSG00000137714	pseudogene on 20q11-q12		Fdx1 (MGI:103224)			
chr11	110600000	130900000	11q23-q24			612629	ADIPQTL4	"Adiponectin, serum level of, quantitative trait locus locus 4"		100271698		between D11S925 and D11S968	"{Adiponectin, serum level of, QTL4}, 612629 (2)"				
chr11	110600000	121300000	11q23			609354	BMND5	Bone mineral density QTL 5		554315		between D11S901 and D11S925	"[Bone mineral density QTL 5], 609354 (2)"				
chr11	110600000	121300000	11q23			612232	CRCS7	"Colorectal cancer, susceptibility to, 7"		100187711		associated with rs3802842	"{Colorectal cancer, susceptibility to, 7}, 612232 (2)"				
chr11	110600000	112700000	11q23.1			132860	EBVM1	Epstein-Barr virus modification site-1									
chr11	110600000	121300000	11q23			137580	GTS	Gilles de la Tourette syndrome				"several loci suspected (e.g., 17q25)"	"Tourette syndrome, 137580 (2), Autosomal dominant"				
chr11	110600000	121300000	11q23			147791	JBS	Jacobsen syndrome				contiguous gene deletion syndrome	"Jacobsen syndrome, 147791 (4), Isolated cases"				
chr11	110600000	121300000	11q23			613387	NAFLD2	"Fatty liver disease, nonalcoholic, susceptibility to, 2"		100462725		"associated with rs2854116, rs2854117"	"{Fatty liver disease, nonalcoholic, susceptibility to, 2}, 613387 (2), Multifactorial"				
chr11	110600000	121300000	11q23			188025	TCPT	"Thrombocytopenia, Paris-Trousseau type (deletion 11q23 syndrome)"				contiguous gene deletion of 11q23	"?Thrombocytopenia, Paris-Trousseau type, 188025 (4), Isolated cases"				
chr11	110600000	121300000	11q23			603040	TSG11	Tumor suppressor gene on chromosome 11		50970			"{Nonsmall cell lung cancer}, 603040 (2)"				
chr11	110600000	114600000	11q23.1-q23.2			194632	ZNF125	Zinc finger protein-125 (HZF-3)									
chr11	111293388	111305047	11q23	11q23.1		615693	COLCA1	Colorectal cancer-associated gene 1	COLCA1	399948							
chr11	111298348	111308734	11q23	11q23.1		615694	COLCA2	Colorectal cancer-associated gene 2	COLCA2	120376	ENSG00000214290	opposite strand from COLCA1		Colca2 (MGI:2685530)			
chr11	111352250	111379670	11q23.1	11q23.1		601206	"POU2AF1, OBF1"	"POU domain, class 2, associating factor 1"	POU2AF1	5450	ENSG00000110777			Pou2af1 (MGI:105086)			
chr11	111383827	111514733	11q23	11q23.1		605673	"BTG4, PC3B"	B-cell translocation gene 4	BTG4	54766	ENSG00000137707			Btg4 (MGI:1860140)			
chr11	111512937	111513020	11q23.1	11q23.1		611374	MIR34B	Micro RNA 34B	MIR34B	407041							
chr11	111513438	111513514	11q23.1	11q23.1		611375	MIR34C	Micro RNA 34C	MIR34C	407042							
chr11	111602390	111726916	11q23.1	11q23.1		608973	"SIK2, KIAA0781"	Salt-inducible kinase 2	SIK2	23235	ENSG00000170145			Sik2 (MGI:2445031)			
chr11	111690272	111766444	11q22-q24	11q23.1		603113	PPP2R1B	"Protein phosphatase 2, structural/regulatory subunit A, beta"	PPP2R1B	5519	ENSG00000137713		"Lung cancer, 211980 (3), Autosomal recessive"	Ppp2r1b (MGI:1920949)			
chr11	111776095	111871580	11q23	11q23.1		606941	"ALG9, DIBD1, CDG1L, GIKANIS"	"Alg9, yeast, homolog of"	ALG9	79796	ENSG00000086848		"Congenital disorder of glycosylation, type Il, 608776 (3), Autosomal recessive; Gillessen-Kaesbach-Nishimura syndrome, 263210 (3), Autosomal recessive"	Alg9 (MGI:1924753)			
chr11	111908619	111913212	11q22.3-q23.1	11q23.1		123590	"CRYAB, CRYA2, CTPP2, CMD1II, CTRCT16, MFM2"	"Crystallin, alpha B"	CRYAB	1410	ENSG00000109846		"Cardiomyopathy, dilated, 1II, 615184 (3), Autosomal dominant; Cataract 16, multiple types, 613763 (3), Autosomal recessive, Autosomal dominant; Myopathy, myofibrillar, 2, 608810 (3), Autosomal dominant; Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related, 613869 (3), Autosomal recessive"	Cryab (MGI:88516)			
chr11	111912735	111914092	11q22-q23	11q23.1		602179	HSPB2	Heat-shock 27kD protein-2	HSPB2	3316	ENSG00000170276			Hspb2 (MGI:1916503)			
chr11	111927143	112022649	11q23.1	11q23.1		610493	"DIXDC1, CCD1, KIAA1735"	DIX domain-containing protein 1	DIXDC1	85458	ENSG00000150764			Dixdc1 (MGI:2679721)			
chr11	112024813	112064277	11q23.1	11q23.1		608770	"DLAT, PDCE2"	Dihydrolipoamide S-acetyltransferase	DLAT	1737	ENSG00000150768		"Pyruvate dehydrogenase E2 deficiency, 245348 (3), Autosomal recessive"	Dlat (MGI:2385311)			
chr11	112086823	112095800	11q23	11q23.1		602690	"SDHD, PGL1, CWS3"	"Succinate dehydrogenase complex, subunit D, integral membrane protein"	SDHD	6392	ENSG00000204370		"Carcinoid tumors, intestinal, 114900 (3), Autosomal dominant; Cowden syndrome 3, 615106 (3); Merkel cell carcinoma, somatic (3); Mitochondrial complex II deficiency, 252011 (3), Autosomal recessive; Paraganglioma and gastric stromal sarcoma, 606864 (3); Paragangliomas 1, with or without deafness, 168000 (3), Autosomal dominant; Pheochromocytoma, 171300 (3), Autosomal dominant"	Sdhd (MGI:1914175)			
chr11	112143250	112164116	11q22.2-q22.3	11q23.1		600953	"IL18, IGIF"	Interleukin-18	IL18	3606	ENSG00000150782			Il18 (MGI:107936)			
chr11	112167371	112172555	Chr.11	11q23.1		605791	TEX12	Testis-expressed gene 12	TEX12	56158	ENSG00000150783			Tex12 (MGI:1913904)			
chr11	112175484	112218928	11q22.3-q23.1	11q23.1		611740	"BCO2, BCDO2"	Beta-carotene oxygenase 2	BCO2	83875	ENSG00000197580			Bco2 (MGI:2177469)			
chr11	112226364	112233972	11q22.3-q23.3	11q23.1		612719	PTS	6-pyruvoyltetrahydropterin synthase	PTS	5805	ENSG00000150787		"Hyperphenylalaninemia, BH4-deficient, A, 261640 (3), Autosomal recessive"	Pts (MGI:1338783)			
chr11	112248152	112260859	11q23.2	11q23.1		611904	"C11orf34, PLET1"	Chromosome 11 open reading frame 34	PLET1	349633	ENSG00000188771			Plet1 (MGI:1923759)			
chr11	112961246	113278435	11q23.1	11q23.2		116930	"NCAM1, MSK39"	Neural cell adhesion molecule 1	NCAM1	4684	ENSG00000149294	"defective in ""staggerer"" in mice"		Ncam1 (MGI:97281)			
chr11	113314528	113385951	11q23.2	11q23.2		610732	"TTC12, TPARM"	Tetratricopeptide repeat domain 12	TTC12	54970	ENSG00000149292			Ttc12 (MGI:2444588)			
chr11	113386013	113400417	11q23.2	11q23.2		608774	ANKK1	Ankyrin repeat and kinase domain containing 1	ANKK1	255239	ENSG00000170209		"Dopamine receptor D2, reduced brain density of (3)"	Ankk1 (MGI:3045301)			
chr11	113409594	113475278	11q23.1	11q23.2		126450	DRD2	Dopamine receptor D2	DRD2	1813	ENSG00000149295	11q22-q23 junction; 150kb 5' to NCAM; centromeric to APOA1; telomeric to STMY1		Drd2 (MGI:94924)			
chr11	113687545	113709810	11q23.3	11q23.2		606751	TMPRSS5	"Transmembrane protease, serine 5"	TMPRSS5	80975	ENSG00000166682			Tmprss5 (MGI:1933407)			
chr11	113733182	113773762	11q23.2	11q23.2		603954	ZW10	"Zeste-white 10, Drosophila, homolog of"	ZW10	9183	ENSG00000086827			Zw10 (MGI:1349478)			
chr11	113797874	113875569	11q23	11q23.2		610748	"USP28, KIAA1515"	Ubiquitin-specific protease 28	USP28	57646	ENSG00000048028			Usp28 (MGI:2442293)			
chr11	113898922	113949118	11q23.1	11q23.2		604654	HTR3B	5-hydroxytryptamine receptor 3B	HTR3B	9177	ENSG00000149305			Htr3b (MGI:1861899)			
chr11	113975074	113990312	11q23.1-q23.2	11q23.2		182139	HTR3	5-hydroxytryptamine (serotonin) receptor-3	HTR3A	3359	ENSG00000166736			Htr3a (MGI:96282)			
chr11	114059575	114256769	11q23.1	11q23.2		176797	"ZBTB16, ZNF145, PLZF"	Zinc finger- and BTB domain-containing protein 16 (promyelocytic leukemia zinc finger)	ZBTB16	7704	ENSG00000109906	fused with RARA in APL of t(11;17) type	"Leukemia, acute promyelocytic, PL2F/RARA type (3); Skeletal defects, genital hypoplasia, and mental retardation, 612447 (3), Autosomal recessive"	Zbtb16 (MGI:103222)			
chr11	114295812	114312515	11q23.1	11q23.2		600008	NNMT	Nicotinamide N-methyltransferase	NNMT	4837	ENSG00000166741		"Homocysteine plasma level, 600008 (2)"	Nnmt (MGI:1099443)			
chr11	114400528	114410609	11q23.1-q23.2	11q23.2		612413	RBM7	RNA-binding motif protein 7	RBM7	10179	ENSG00000076053			Rbm7 (MGI:1914260)			
chr11	114439385	114450278	11q23.1-q23.2	11q23.2		607149	"REXO2, RFN"	"RNA exonuclease 2, S. cerevisiae, homolog of"	REXO2	25996	ENSG00000076043			Rexo2 (MGI:1888981)			
chr11	114600000	130900000	11q23.3-q24			607086	"AAT1, FAA1"	"Aortic aneurysm, familial thoracic 1"		252842			"Aortic aneurysm, familial thoracic 1, 607086 (2)"				
chr11	114600000	121300000	11q23.3			605201	"HDLCQ14, HYLAP"	High density lipoprotein cholesterol level quantitative trait locus 14		56801			"High density lipoprotein cholesterol level QTL14, 605201 (2)"				
chr11	115173624	115504522	11q23.2	11q23.3		605686	"CADM1, IGSF4, TSLC1"	Cell adhesion molecule 1	CADM1	23705	ENSG00000182985			Cadm1 (MGI:1889272)			
chr11	116778188	116789271	11q23.3	11q23.3		603901	"ZPR1, ZNF259"	ZPR1 zinc finger protein	ZPR1	8882	ENSG00000109917			Zpr1 (MGI:1330262)			
chr11	116789369	116792419	11q23	11q23.3		606368	APOA5	Apolipoprotein A-V	APOA5	116519	ENSG00000110243	"proximal to APOA1, APOC3, APOA4"	"Hyperchylomicronemia, late-onset, 144650 (3), Autosomal dominant; {Hypertriglyceridemia, susceptibility to}, 145750 (3), Autosomal dominant"	Apoa5 (MGI:1913363)			
chr11	116820701	116823294	11q23	11q23.3		107690	APOA4	Apolipoprotein A-IV	APOA4	337	ENSG00000110244	12 kb 3' to APOA1		Apoa4 (MGI:88051)			
chr11	116829891	116833073	11q23	11q23.3		107720	"APOC3, HALP2"	Apolipoprotein C-III	APOC3	345	ENSG00000110245	2.6kb 3' to APOA1	"Apolipoprotein C-III deficiency, 614028 (3)"				
chr11	116835750	116837949	11q23	11q23.3		107680	APOA1	Apolipoprotein A-I	APOA1	335	ENSG00000118137		"Amyloidosis, 3 or more types, 105200 (3), Autosomal dominant; ApoA-I and apoC-III deficiency, combined (3); Corneal clouding, autosomal recessive (3); Hypoalphalipoproteinemia, 604091 (3)"	Apoa1 (MGI:88049)			
chr11	116843401	117098452	11q23.3	11q23.3		614776	"SIK3, KIAA0999"	Salt-inducible kinase 3	SIK3	23387	ENSG00000160584			Sik3 (MGI:2446296)			
chr11	117144283	117178172	11q23	11q23.3		602508	PAFAH1B2	"Platelet-activating factor acetylhydrolase, isoform Ib, beta subunit"	PAFAH1B2	5049	ENSG00000168092			Pafah1b2 (MGI:108415)			
chr11	117179222	117197444	11q23.3	11q23.3		617551	SIDT2	"SID1 transmembrane family, member 2"	SIDT2	51092	ENSG00000149577			Sidt2 (MGI:2446134)			
chr11	117199293	117207464	11q23.2	11q23.3		600818	"TAGLN, SMCC, SM22"	Transgelin	TAGLN	6876	ENSG00000149591			Tagln (MGI:106012)			
chr11	117201155	117232524	11q23.3	11q23.3		604872	"PCSK7, PC8, PC7, LPC"	"Proprotein convertase, subtilisin/kexin-type, 7"	PCSK7	9159	ENSG00000160613			Pcsk7 (MGI:107421)			
chr11	117285685	117316255	11q23.3	11q23.3		604252	"BACE1, BACE"	"Beta-site amyloid beta A4 precursor protein-cleaving enzyme (secretase, beta; memapsin 2)"	BACE1	23621	ENSG00000186318			Bace1 (MGI:1346542)			
chr11	117291345	117292169	11q23.3	11q23.3		614263	BACE1AS	BACE1 antisense RNA	BACE1-AS	100379571							
chr11	117316345	117413265	11q23.3	11q23.3		614848	"CEP164, KIAA1052"	"Centrosomal protein, 164kD"	CEP164	22897	ENSG00000110274		"Nephronophthisis 15, 614845 (3), Autosomal recessive"	Cep164 (MGI:2384878)			
chr11	117427771	117797260	11q23	11q23.3		611782	"DSCAML1, KIAA1132"	Down syndrome cell adhesion molecule-like 1	DSCAML1	57453	ENSG00000177103			Dscaml1 (MGI:2150309)			
chr11	117820074	117828091	11q23	11q23.3		601814	"FXYD2, ATP1G1, HOMG2"	"FXYD domain-containing ion transport regulator 2 (sodium-potassium-ATPase, gamma polypeptide)"	FXYD2	486	ENSG00000137731		"Hypomagnesemia 2, renal, 154020 (3), Autosomal dominant"				
chr11	117836975	117877485	Chr.11	11q23.3		606683	FXYD6	FXYD domain-containing ion transport regulator 6	FXYD6	53826	ENSG00000137726			Fxyd6 (MGI:1890226)			
chr11	117900640	117929452	11q23	11q23.3		610050	"TMPRSS13, MSPL, MSPS"	"Transmembrane protein, serine 13"	TMPRSS13	84000	ENSG00000137747			Tmprss13 (MGI:2682935)			
chr11	117986390	118001482	11q23.3	11q23.3		146933	"IL10RA, IL10R, IBD28"	"Interleukin-10 receptor, alpha"	IL10RA	3587	ENSG00000110324		"Inflammatory bowel disease 28, early onset, autosomal recessive, 613148 (3), Autosomal recessive"	Il10ra (MGI:96538)			
chr11	118077011	118125504	11q23.3	11q23.3		606565	TMPRSS4	"Transmembrane protease, serine 4"	TMPRSS4	56649	ENSG00000137648			Tmprss4 (MGI:2384877)			
chr11	118133376	118152914	11q23	11q23.3		608256	"SCN4B, LQT10, ATFB17"	"Sodium channel, voltage-gated, type IV, beta subunit"	SCN4B	6330	ENSG00000177098		"Atrial fibrillation, familial, 17, 611819 (3), Autosomal dominant; Long QT syndrome-10, 611819 (3), Autosomal dominant"	Scn4b (MGI:2687406)			
chr11	118162803	118176621	11q23	11q23.3		601327	"SCN2B, ATFB14"	"Sodium channel, voltage-gated, type II, beta polypeptide"	SCN2B	6327	ENSG00000149575		"Atrial fibrillation, familial, 14, 615378 (3), Autosomal dominant"	Scn2b (MGI:106921)			
chr11	118193726	118225093	11q23	11q23.3		609770	"AMICA1, JAML"	"Adhesion molecule, interacts with CXADR antigen 1"	JAML	120425	ENSG00000160593			Jaml (MGI:2685484)			
chr11	118226689	118252367	11q23.3	11q23.3		611707	MPZL3	Myelin protein zero-like 3	MPZL3	196264	ENSG00000160588			Mpzl3 (MGI:2442647)			
chr11	118253415	118264535	11q24	11q23.3		604873	"MPZL2, EVA1, EVA"	Myelin protein zero-like 2	MPZL2	10205	ENSG00000149573			Mpzl2 (MGI:1289160)			
chr11	118304579	118316174	11q23	11q23.3		186830	"CD3E, IMD18"	"CD3E antigen, epsilon polypeptide (TiT3 complex)"	CD3E	916	ENSG00000198851		"Immunodeficiency 18, 615615 (3), Autosomal recessive; Immunodeficiency 18, SCID variant, 615615 (3), Autosomal recessive"	Cd3e (MGI:88332)			
chr11	118339073	118342743	11q23	11q23.3		186790	"CD3D, T3D, IMD19"	"CD3D antigen, delta polypeptide (TiT3 complex)"	CD3D	915	ENSG00000167286	3 CD3 genes in 50kb	"Immunodeficiency 19, 615617 (3), Autosomal recessive"	Cd3d (MGI:88331)			
chr11	118344343	118353781	11q23	11q23.3		186740	"CD3G, IMD17"	"CD3G antigen, gamma polypeptide (TiT3 complex)"	CD3G	917	ENSG00000160654		"Immunodeficiency 17, CD3 gamma deficient, 615607 (3), Autosomal recessive"	Cd3g (MGI:88333)			
chr11	118359580	118399210	Chr.11	11q23.3		603753	"UBE4A, UFD2, E4"	Ubiquitination factor E4A	UBE4A	9354	ENSG00000110344			Ube4a (MGI:2154580)			
chr11	118401388	118409846	11q22.3	11q23.3		617473	ATP5JG	"ATP synthase, H+ transporting, mitochondrial F0 complex, subunit G"	ATP5MG	10632	ENSG00000167283			Atp5l (MGI:1351597)			
chr11	118436489	118526831	11q23	11q23.3		159555	"KMT2A, MLL, HRX, HTRX1, WDSTS"	Lysine (K)-specific methyltransferase 2E	KMT2A	4297	ENSG00000118058	"fuses with ENL, AF4, AF9, GMPS"	"Leukemia, myeloid/lymphoid or mixed-lineage, 159555 (2), Autosomal dominant; Wiedemann-Steiner syndrome, 605130 (3), Autosomal dominant"	Kmt2a (MGI:96995)			
chr11	118531087	118546597	11q23.3	11q23.3		613934	TMEM25	Transmembrane protein 25	TMEM25	84866	ENSG00000149582			Tmem25 (MGI:1918937)			
chr11	118572386	118603032	11q23.3	11q23.3		600820	"ARCN1, SRMMD"	Archain 1	ARCN1	372	ENSG00000095139	60kb telomeric to MLL	"Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay, 617164 (3), Autosomal dominant"	Arcn1 (MGI:2387591)			
chr11	118606295	118658037	11q23.3	11q23.3		612834	"PHLDB1, LL5A, KIAA0638"	"Pleckstrin homology-like domain, family B, member 1"	PHLDB1	23187	ENSG00000019144			Phldb1 (MGI:2143230)			
chr11	118658231	118679671	11q23	11q23.3		275360	"TREH, TREHD"	Trehalase	TREH	11181	ENSG00000118094		"Trehalase deficiency, 612119 (3), Autosomal recessive"	Treh (MGI:1926230)			
chr11	118747762	118791695	11q23.3	11q23.3		600326	"DDX6, HLR2"	"DEAD/H box-6 (RNA helicase, 54kD)"	DDX6	1656	ENSG00000110367			Ddx6 (MGI:104976)			
chr11	118883765	118896270	11q23.3	11q23.3		601613	"CXCR5, BLR1"	"Chemokine, CXC motif, receptor 5"	CXCR5	643	ENSG00000160683			Cxcr5 (MGI:103567)			
chr11	118896139	118926071	11q23.3	11q23.3		609004	BCL9L	B-cell CLL/lymphoma 9-like	BCL9L	283149	ENSG00000186174			Bcl9l (MGI:1933114)			
chr11	118956297	118958558	11q23.3	11q23.3		611558	"UPK2, UP2, UPII"	Uroplakin 2	UPK2	7379	ENSG00000110375			Upk2 (MGI:98913)			
chr11	118971397	118981600	11q23.3	11q23.3		615755	"FOXR1, FOXN5"	Forkhead box R1	FOXR1	283150	ENSG00000176302			Foxr1 (MGI:2685961)			
chr11	119015711	119018346	11q23.3	11q23.3		180465	RPS25	Ribosomal protein S25	RPS25	6230	ENSG00000118181			Rps25 (MGI:1922867)			
chr11	119018468	119023673	11q23.3	11q23.3		610971	TRAPPC4	"Trafficking protein particle complex, subunit 4 (synbindin)"	TRAPPC4	51399	ENSG00000196655			Trappc4 (MGI:1926211)			
chr11	119024350	119030905	11q23	11q23.3		602671	"SLC37A4, G6PT1"	"Solute carrier family 37 (glucose-6-phosphate transporter), member 4"	SLC37A4	2542	ENSG00000137700		"Glycogen storage disease Ib, 232220 (3), Autosomal recessive; Glycogen storage disease Ic, 232240 (3), Autosomal recessive"	Slc37a4 (MGI:1316650)			
chr11	119044184	119057245	Chr.11	11q23.3		601746	HYOU1	Hypoxia-upregulated 1	HYOU1	10525	ENSG00000149428			Hyou1 (MGI:108030)			
chr11	119067751	119081977	11q23.3	11q23.3		608549	"VPS11, HLD12"	"Vacuolar protein sorting 11, yeast, homolog of"	VPS11	55823	ENSG00000160695		"Leukodystrophy, hypomyelinating, 12, 616683 (3), Autosomal recessive"	Vps11 (MGI:1918982)			
chr11	119084863	119093548	11q23.3	11q23.3		609806	"HMBS, PBGD, UPS"	Hydroxymethylbilane synthase	HMBS	3145	ENSG00000256269		"Porphyria, acute intermittent, 176000 (3), Autosomal dominant; Porphyria, acute intermittent, nonerythroid variant, 176000 (3), Autosomal dominant"	Hmbs (MGI:96112)			
chr11	119093873	119095466	11q23.2-q23.3	11q23.3		601772	H2AX	H2AX histone	H2AFX	3014	ENSG00000188486			H2afx (MGI:102688)			
chr11	119096502	119102074	11q23.3	11q23.3		191350	"DPAGT1, DPAGT2, DGPT, CDG1J, CMSTA2, CMS13"	Dolichyl-phosphate N-acetylglucosamine phosphotransferase	DPAGT1	1798	ENSG00000172269		"Congenital disorder of glycosylation, type Ij, 608093 (3), Autosomal recessive; Myasthenic syndrome, congenital, 13, with tubular aggregates, 614750 (3), Autosomal recessive"	Dpagt1 (MGI:1196396)			
chr11	119106751	119118346	11q23.3	11q23.3		617582	"C2CD2L, TMEM24"	C2 calcium-dependent domain-containing protein 2-like	C2CD2L	9854	ENSG00000172375			C2cd2l (MGI:1919014)			
chr11	119121522	119135054	Chr.11	11q23.3		607099	MIZF	MBD2-interaction zinc finger protein	HINFP	25988	ENSG00000172273			Hinfp (MGI:2429620)			
chr11	119149039	119162665	11q23.3	11q23.3		607784	"ABCG4, WHITE2"	"ATP-binding cassette, subfamily G, member 4"	ABCG4	64137	ENSG00000172350			Abcg4 (MGI:1890594)			
chr11	119168333	119184015	11q23.3	11q23.3		611947	"NLRX1, NOD9, CLR11.3"	NLR family member X1	NLRX1	79671	ENSG00000160703			Nlrx1 (MGI:2429611)			
chr11	119185456	119190222	11q23	11q23.3		607146	"PDZD3, IKEPP"	PDZ domain-containing 3	PDZD3	79849	ENSG00000172367			Pdzd3 (MGI:2429554)			
chr11	119206275	119308148	11q23.3	11q23.3		165360	"CBL, CBL2, NSLL"	Cas-Br-M ecotropic retroviral transforming sequence (Oncogene CBL2)	CBL	867	ENSG00000110395	mutation identified in 1 JMML family	"?Juvenile myelomonocytic leukemia, 607785 (3), Autosomal dominant, Somatic mutation; Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia, 613563 (3), Autosomal dominant"	Cbl (MGI:88279)			
chr11	119305758	119317129	11q23.3	11q23.3		155735	"MCAM, MUC18, CD146"	Melanoma adhesion molecule	MCAM	4162	ENSG00000076706			Mcam (MGI:1933966)			
chr11	119334499	119337313	11q23	11q23.3		606130	RNF26	RING finger protein-26	RNF26	79102	ENSG00000173456			Rnf26 (MGI:2388131)			
chr11	119338933	119346672	11q23.3	11q23.3		608752	"C1QTNF5, CTRP5, LORD"	C1q- and tumor necrosis factor-related protein 5	C1QTNF5	114902	ENSG00000223953		"Retinal degeneration, late-onset, autosomal dominant, 605670 (3), Autosomal dominant"	C1qtnf5 (MGI:2385958)			
chr11	119338933	119346672	11q23	11q23.3		606227	"MFRP, MCOP5, NNO2"	Membrane-type frizzled-related protein	MFRP	83552	ENSG00000235718		"Microphthalmia, isolated 5, 611040 (3), Autosomal recessive; Nanophthalmos 2, 609549 (3)"	Mfrp (MGI:2385957)			
chr11	119417940	119424984	11q23.3	11q23.3		188230	THY1	Thy-1 T-cell antigen	THY1	7070	ENSG00000154096			Thy1 (MGI:98747)			
chr11	119638097	119728724	11q23-q24	11q23.3		600644	"NECTIN1, PVRL1, HVEC, PVRR1, PRR1, ED4, OFC7, CLPED1"	Nectin 1	NECTIN1	5818	ENSG00000110400		"Cleft lip/palate-ectodermal dysplasia syndrome, 225060 (3), Autosomal recessive; Orofacial cleft 7, 225060 (3), Autosomal recessive"	Nectin1 (MGI:1926483)			
chr11	120111274	120138154	11q23.3	11q23.3		610658	"TRIM29, ATDC"	Tripartite motif-containing protein 29	TRIM29	23650	ENSG00000137699			Trim29 (MGI:1919419)			
chr11	120236639	120319943	11q23.3	11q23.3		607394	"POU2F3, OCT11"	"POU domain, class 2, transcription factor 3"	POU2F3	25833	ENSG00000137709			Pou2f3 (MGI:102565)			
chr11	120336275	120489935	11q23.3	11q23.3		604763	"ARHGEF12, LARG, KIAA0382"	"Rho guanine nucleotide exchange factor 12, leukemia-associated"	ARHGEF12	23365	ENSG00000196914	fused with MLL in AML		Arhgef12 (MGI:1916882)			
chr11	120511745	120988804	11q22.3	11q23.3		600282	GRIK4	"Glutamate receptor, ionotropic, kainate 4"	GRIK4	2900	ENSG00000149403			Grik4 (MGI:95817)			
chr11	121024071	121090775	11q23.3	11q23.3		610451	"LRRC35, EL"	Leucine-rich repeat-containing protein 35	TBCEL	219899	ENSG00000154114			Tbcel (MGI:1925543)			
chr11	121102665	121190805	11q22-q24	11q23.3		602574	"TECTA, DFNA8, DFNA12, DFNB21"	"Tectorin, alpha"	TECTA	7007	ENSG00000109927		"Deafness, autosomal dominant 8/12, 601543 (3), Autosomal dominant; Deafness, autosomal recessive 21, 603629 (3), Autosomal recessive"	Tecta (MGI:109575)			
chr11	121292678	121313409	11q23.3	11q23.3-q24.1		602286	"SC5DL, ERG3"	Sterol C5-desaturase-like	SC5D	6309	ENSG00000109929		"Lathosterolosis, 607330 (3), Autosomal recessive"	Sc5d (MGI:1353611)			
chr11	121300000	135086622	11q24-q25			612161	ANIB7	"Aneurysm, intracranial berry, 7"		100188885		between rs618176 and rs1940033	"Aneurysm, intracranial berry, 7, 612161 (2)"				
chr11	121300000	124000000	11q24.1			612559	CLLS5	"Leukemia, chronic lymphocytic susceptibility to, 5"		100270644		associated with rs735665	"{Leukemia, chronic lymphocytic susceptibility to, 5}, 612559 (2)"				
chr11	121300000	130900000	11q24			609670	MGR9	"Migraine with aura, susceptibility to, 9"		100415943		max lod at GATA64D03	"{Migraine with aura, susceptibility to, 9}, 609670 (2)"				
chr11	121300000	130900000	11q24			609469	NEDE	"Nephropathy, progressive, with deafness"		619410		max lod at D11S4464	"Nephropathy, progressive, with deafness, 609469 (2)"				
chr11	121452202	121633761	11q23.2-q24.2	11q24.1		602005	"SORL1, LR11, SORLA"	"Sortilin-related receptor, L(DLR class) A repeats-containing"	SORL1	6653	ENSG00000137642			Sorl1 (MGI:1202296)			
chr11	122028328	122422870	11q24.1	11q24.1		615965	"MIR100HG, AGD1"	"MIR100-LET7A2 cluster host gene, noncoding"	MIR100HG	399959							
chr11	122099756	122099843	11q24.1	11q24.1		610104	"MIR125B1, MIRN125B1"	Micro RNA 125B-1	MIR125B1	406911							
chr11	122115353	122116214	11q24.1	11q24.1		608853	"BLID, BRCC@"	BH3-like motif-containing cell death inducer	BLID	414899	ENSG00000259571	distal to SORL1					
chr11	122146521	122146592	11q24.1	11q24.1		612142	"MIRLET7A2, LET7A2, MIRNLET7A2"	Micro RNA let7a2	MIRLET7A2	406882							
chr11	122152228	122152307	11q24.1	11q24.1		613186	"MIR100, MIRN100"	Micro RNA 100	MIR100	406892							
chr11	122655689	122814478	11q24.1	11q24.1		609201	"UBASH3B, STS1, KIAA1959, P70"	Ubiquitin-associated and SH3 domain-containing protein B	UBASH3B	84959	ENSG00000154127			Ubash3b (MGI:1920078)			
chr11	122838418	122872642	11q22-q23	11q24.1		612597	CRTAM	Cytotoxic and regulatory T-cell molecule	CRTAM	56253	ENSG00000109943			Crtam (MGI:1859822)			
chr11	122881639	122963861	11q24.1	11q24.1		617594	"C11orf63, JHY"	Chromosome 11 open reading frame 63	JHY	79864	ENSG00000109944			Jhy (MGI:1918239)			
chr11	122977648	122981670	11q24.1	11q24.1		611074	BSX1	"Brain-specific homeobox, mouse, homolog of"	BSX	390259	ENSG00000188909			Bsx (MGI:2669849)			
chr11	123057491	123062365	11q23.3-q25	11q24.1		600816	"HSPA8, HSP73"	Heat-shock 70kD protein-8 (HSP73)	HSPA8	3312	ENSG00000109971			Hspa8 (MGI:105384)			
chr11	123072005	123195304	11q24.1	11q24.1		611693	"CLMP, ASAM, ACAM, CSBS"	Coxsackievirus- and adenovirus receptor-like membrane protein	CLMP	79827	ENSG00000166250		"Congenital short bowel syndrome, 615237 (3), Autosomal recessive"	Clmp (MGI:1918816)			
chr11	123629186	123654606	11q23.3	11q24.1		608214	"SCN3B, SCNB3, BRGDA7, ATFB16"	"Sodium channel, voltage-gated, type III, beta subunit"	SCN3B	55800	ENSG00000166257		"Atrial fibrillation, familial, 16, 613120 (3), Autosomal dominant; Brugada syndrome 7, 613120 (3), Autosomal dominant"	Scn3b (MGI:1918882)			
chr11	123723926	123741682	11q23.3	11q24.1		603430	ZNF202	Zinc finger protein-202	ZNF202	7753	ENSG00000166261			Zfp202 (MGI:1933401)			
chr11	124115403	124146911	11q23	11q24.2		602929	"VWA5A, LOH11CR2A, BCSC1"	von Willebrand factor A domain-containing protein 5A	VWA5A	4013	ENSG00000110002			Vwa5a (MGI:1915026)			
chr11	124611556	124620355	11q24.2	11q24.2		608422	"PANX3, PX3"	Pannexin 3	PANX3	116337	ENSG00000154143			Panx3 (MGI:1918881)			
chr11	124622845	124635925	11q24.2	11q24.2		610614	"TBRG1, NIAM"	Transforming growth factor-beta regulator 1	TBRG1	84897	ENSG00000154144			Tbrg1 (MGI:1100877)			
chr11	124635788	124676302	11q24	11q24.2		610079	"SIAE, AIS6"	Sialic acid acetylesterase	SIAE	54414	ENSG00000110013		"{Autoimmune disease, susceptibility to, 6}, 613551 (3)"	Siae (MGI:104803)			
chr11	124739932	124747205	11q24	11q24.2		602350	NRGN	Neurogranin	NRGN	4900	ENSG00000154146						
chr11	124747471	124752271	11q24	11q24.2		606011	"VSIG2, CTXL"	V-set and immunoglobulin domains-containing protein 2	VSIG2	23584	ENSG00000019102			Vsig2 (MGI:1928009)			
chr11	124753122	124762326	11q24.2	11q24.2		614281	ESAM	Endothelial cell adhesion molecule	ESAM	90952	ENSG00000149564			Esam (MGI:1916774)			
chr11	124865408	124881473	11q23-q25	11q24.2		608630	"ROBO3, RBIG1, RIG1, HGPPS1"	"Roundabout, Drosophila, homolog of, 3"	ROBO3	64221	ENSG00000154134		"Gaze palsy, familial horizontal, with progressive scoliosis, 1, 607313 (3), Autosomal recessive"	Robo3 (MGI:1343102)			
chr11	124884217	124897934	11q24.2	11q24.2		607528	ROBO4	"Roundabout, Drosophila, homolog of, 4"	ROBO4	54538	ENSG00000154133			Robo4 (MGI:1921394)			
chr11	124919243	124936411	11q24	11q24.2		611642	"HEPACAM, MLC2A, MLC2B"	Hepatocyte cell adhesion molecule	HEPACAM	220296	ENSG00000165478		"Megalencephalic leukoencephalopathy with subcortical cysts 2A, 613925 (3), Autosomal recessive; Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation, 613926 (3), Autosomal dominant"	Hepacam (MGI:1920177)			
chr11	124919249	124920676	11q24.2	11q24.2		611641	HEPN1	Cancer susceptibility gene HEPN1	HEPN1	641654	ENSG00000221932						
chr11	125111996	125433388	11q24-q25	11q24.2		613066	"PKNOX2, PREP2"	PBX/Knotted 1 homeobox 2	PKNOX2	63876	ENSG00000165495			Pknox2 (MGI:2445415)			
chr11	125445744	125496309	11q24.2	11q24.2		604825	FEZ1	Fasciculation and elongation protein zeta 1	FEZ1	9638	ENSG00000149557			Fez1 (MGI:2670976)			
chr11	125569215	125584688	11q23	11q24.2		605170	"EI24, PIG8, EPG4"	Etoposide-induced 1.4 mRNA	EI24	9538	ENSG00000149547			Ei24 (MGI:108090)			
chr11	125592794	125622758	11q23.3	11q24.2		601134	"STT3A, ITM1, TMC"	"STT3A, subunit of the oligosaccharyltransferase complex (catalytic)"	STT3A	3703	ENSG00000134910	mutation identified in 1 family	"?Congenital disorder of glycosylation, type Iw, 615596 (3), Autosomal recessive"	Stt3a (MGI:105124)			
chr11	125624909	125676255	11q22-q23	11q24.2		603078	"CHEK1, CHK1"	"Checkpoint kinase 1, S. pombe, homolog of"	CHEK1	1111	ENSG00000149554			Chek1 (MGI:1202065)			
chr11	125672333	125680897	11p12-q13	11q24.2		102525	ACRV1	Acrosomal vesicle protein-1	ACRV1	56	ENSG00000134940			Acrv1 (MGI:104590)			
chr11	125746292	125749847	11q24	11q24.2		606861	PATE	Prostate- and testis-expressed gene	PATE1	160065	ENSG00000171053			Pate1 (MGI:4936886)			
chr11	125883613	125900645	11q24.2	11q24.2		610693	"HYLS1, FLJ32915"	HYLS1 gene	HYLS1	219844	ENSG00000198331		"Hydrolethalus syndrome, 236680 (3), Autosomal recessive"	Hyls1 (MGI:1924082)			
chr11	125893484	125903277	11q24.2	11q24.2		616283	"PUS3, MRT55"	Pseudouridylate synthase 3	PUS3	83480	ENSG00000110060	mutation identified in 1 MRT55 family	"?Mental retardation, autosomal recessive 55, 617051 (3), Autosomal recessive"	Pus3 (MGI:1914299)			
chr11	125903375	125923403	11q24	11q24.2		607663	GRTH	Gonadotropin-regulated testicular RNA helicase	DDX25	29118	ENSG00000109832			Ddx25 (MGI:1353582)			
chr11	125956812	126063334	11q24.2	11q24.2		608707	"CDON, CDO, HPE11"	Cell adhesion molecule-related/downregulated by oncogenes	CDON	50937	ENSG00000064309		"Holoprosencephaly 11, 614226 (3), Autosomal dominant, Isolated cases"	Cdon (MGI:1926387)			
chr11	126202093	126211691	11q24.2	11q24.2		617488	RPUSD4	RNA pseudouridylate synthase domain-containing protein 4	RPUSD4	84881	ENSG00000165526			Rpusd4 (MGI:1919239)			
chr11	126211413	126264539	11q24.2	11q24.2		616587	FAM118B	"Family with sequence similarity 118, member B"	FAM118B	79607	ENSG00000197798			Fam118b (MGI:1924483)			
chr11	126255150	126268981	11q23-q24	11q24.2		182180	"SRPRA, SRPR, DP"	"Signal recognition particle receptor, alpha subunit"	SRPRA	6734	ENSG00000182934			Srpr (MGI:1914648)			
chr11	126269039	126278131	11q24.2	11q24.2		613622	FOXRED1	FAD-dependent oxidoreductase domain-containing protein 1	FOXRED1	55572	ENSG00000110074		"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Foxred1 (MGI:2446262)			
chr11	126283086	126294932	11q23-q24	11q24.2		606252	"TIRAP, BACTS1"	TIR domain-containing adaptor protein	TIRAP	114609	ENSG00000150455		"{Bacteremia, protection against}, 614382 (3); {Malaria, protection against}, 611162 (3); {Pneumococcal disease, invasive, protection against}, 610799 (3); {Tuberculosis, protection against}, 607948 (3)"	Tirap (MGI:2152213)			
chr11	126303751	126350004	11q24.2	11q24.2		610534	"DCPS, HINT5, DCS1, ARS"	"Decapping enzyme, scavenger"	DCPS	28960	ENSG00000110063		"Al-Raqad syndrome, 616459 (3), Autosomal recessive"	Dcps (MGI:1916555)			
chr11	126355644	126414640	11q24.2	11q24.2		104240	"ST3GAL4, SIAT4C, SIAT4, CGS23, NANTA3"	"ST3 beta-galactoside alpha-2,3-sialyltransferase 4"	ST3GAL4	6484	ENSG00000110080			St3gal4 (MGI:1316743)			
chr11	126423492	127003459	11q24.2	11q24.2		607761	"KIRREL3, NEPH2, KIAA1867, KIRRE, MRD4"	Kin of IRRE-like 3	KIRREL3	84623	ENSG00000149571		"Mental retardation, autosomal dominant 4, 612581 (3)"	Kirrel3 (MGI:1914953)			
chr11	128458760	128587592	11q23.3	11q24.3		164720	ETS1	Avian erythroblastosis virus E26 (v-ets) oncogene homolog-1	ETS1	2113	ENSG00000134954	shown by HSR; 19cM distal to THY1; Ewing sarcoma breakpoint region-2 splices to EWSR1		Ets1 (MGI:95455)			
chr11	128685262	128813266	11q24	11q24.3		193067	"FLI1, BDPLT21"	Friend leukemia virus integration 1	FLI1	2313	ENSG00000151702	fused with EWS in Ewing sarcoma	"Bleeding disorder, platelet-type, 21, 617443 (3), Autosomal recessive, Autosomal dominant"	Fli1 (MGI:95554)			
chr11	128691671	128696022	11q24.1	11q24.3		615815	"SENCR, lncRNA9"	Smooth muscle- and endothelial cell-enriched migration/differentiation-associated long noncoding RNA	SENCR	100507392							
chr11	128838013	128867372	11q24	11q24.3		600359	"KCNJ1, ROMK1"	"Potassium inwardly-rectifying channel, subfamily J, member 1"	KCNJ1	3758	ENSG00000151704		"Bartter syndrome, type 2, 241200 (3), Autosomal recessive"	Kcnj1 (MGI:1927248)			
chr11	128891331	128921162	11q24	11q24.3		600734	"KCNJ5, GIRK4, KATP1, LQT13"	"Potassium inwardly-rectifying channel, subfamily J, member 5"	KCNJ5	3762	ENSG00000120457		"Hyperaldosteronism, familial, type III, 613677 (3), Autosomal dominant; Long QT syndrome 13, 613485 (3), Autosomal dominant"	Kcnj5 (MGI:104755)			
chr11	128934731	128944232	11q24	11q24.3		605426	"TP53AIP1, P53AIP1"	Tumor protein p53-regulated apoptosis-inducing protein 1	TP53AIP1	63970	ENSG00000120471						
chr11	128965059	129279166	11q24.3	11q24.3		608541	"ARHGAP32, RICS, GRIT, p200RHOGAP, p250GAP"	Rho GTPase activating protein 32	ARHGAP32	9743	ENSG00000134909			Arhgap32 (MGI:2450166)			
chr11	129295202	129296614	11q23.1-q23.2	11q24.3		194630	ZNF123	Zinc finger protein-123 (HZF-1)	ZNF123P	100188891							
chr11	129375236	129452278	11q25	11q24.3		604823	BARX2	BarH-like homeo box gene 2	BARX2	8538	ENSG00000043039			Barx2 (MGI:109617)			
chr11	129863772	129895595	11q24-q25	11q24.3		164013	NFRKB	Nuclear factor related to kappa B-binding protein	NFRKB	4798	ENSG00000170322	most telomeric 11q marker		Nfrkb (MGI:2442410)			
chr11	130069820	130144810	11q24	11q24.3		104776	APLP2	Amyloid beta (A4) precursor-like protein-2	APLP2	334	ENSG00000084234			Aplp2 (MGI:88047)			
chr11	130159786	130210361	11q24-q25	11q24.3		606797	"ST14, MTSP1, ARCI11"	Suppression of tumorigenicity 14	ST14	6768	ENSG00000149418		"Ichthyosis, congenital, autosomal recessive 11, 602400 (3), Autosomal recessive"	St14 (MGI:1338881)			
chr11	130404922	130428992	11q25	11q24.3		605175	"ADAMTS8, METH2"	"A disintegrin-like and metalloproteinase with thrombospondin type-1 motif, 8"	ADAMTS8	11095	ENSG00000134917			Adamts8 (MGI:1353468)			
chr11	130448875	130478214	11q24.3	11q24.3		607509	ADAMTS15	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 15"	ADAMTS15	170689	ENSG00000166106			Adamts15 (MGI:2449569)			
chr11	130900000	135086622	11q25-qter			604060	DFNB20	"Deafness, autosomal recessive 20"	DFNB20	1713			"Deafness, autosomal recessive 20, 604060 (2), Autosomal recessive"				
chr11	130900000	135086622	11q25			602782	"HJCD, HCLAP"	Histiocytosis with joint contractures and sensorineural deafness					"Histiocytosis-lymphadenopathy plus syndrome, 602782 (3), Autosomal recessive"				
chr11	131370307	132336821	11q25	11q25		607938	"NTM, HNT"	Neurotrimin	NTM	50863	ENSG00000182667			Ntm (MGI:2446259)			
chr11	132403360	133532611	11q25	11q25		600632	OPCML	Opioid-binding protein/cell adhesion molecule-like	OPCML	4978	ENSG00000183715		"{Ovarian cancer, somatic}, 167000 (3)"	Opcml (MGI:97397)			
chr11	133835929	133845537	11q25	11q25		609805	SPATA19	Spermatogenesis-associated protein 19	SPATA19	219938	ENSG00000166118			Spata19 (MGI:1922719)			
chr11	133908563	133956959	11q25	11q25		613773	"IGSF9B, KIAA1030"	"Immunoglobulin superfamily, member 9B"	IGSF9B	22997	ENSG00000080854			Igsf9b (MGI:2685354)			
chr11	134068924	134151756	11q25	11q25		606871	JAM3	Junctional adhesion molecule 3	JAM3	83700	ENSG00000166086		"Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, 613730 (3), Autosomal recessive"	Jam3 (MGI:1933825)			
chr11	134152441	134225453	11q25	11q25		609276	"NCAPD3, CAPD3, KIAA0056"	Non-SMC condensin II complex subunit D3	NCAPD3	23310	ENSG00000151503			Ncapd3 (MGI:2142989)			
chr11	134224604	134247791	11q25	11q25		610027	VPS26B	"Vacuolar protein sorting 26, yeast, homolog of, B"	VPS26B	112936	ENSG00000151502			Vps26b (MGI:1917656)			
chr11	134248264	134253406	11q25	11q25		613739	"THYN1, HSPC144, THY28"	Thymocyte nuclear protein 1	THYN1	29087	ENSG00000151500			Thyn1 (MGI:1925112)			
chr11	134253537	134265857	11q25	11q25		604773	ACAD8	"Acyl-CoA dehydrogenase family, member 8"	ACAD8	27034	ENSG00000151498		"Isobutyryl-CoA dehydrogenase deficiency, 611283 (3)"	Acad8 (MGI:1914198)			
chr11	134378503	134411985	11q25	11q25		151290	"B3GAT1, GLCATP, CD57, HNK1"	"Beta-1,3-glucuronyltransferase 1"	B3GAT1	27087	ENSG00000109956			B3gat1 (MGI:1924148)			
chr11	0	135086622	Chr.11			606049	AOCH	"Acromegaloid features, overgrowth, cleft palate, and hernia"		93956		"pericentric inversion (46,XY,inv(11)(p15.3;q23.3))"	"Acromegaloid features, overgrowth, cleft palate, and hernia, 606049 (2)"				
chr12	0	35500000	12p			107920	KAR	Aromatic alpha-keto acid reductase				?same as MDH1					
chr12	0	10000000	12p13.3			612372	MAFD9	Major affective disorder 9		100196917		associated with rs1006737	"{Major affective disorder-9, susceptibility to}, 612372 (2)"				
chr12	0	35500000	12p			601803	PKS	Pallister-Killian syndrome					"Pallister-Killian syndrome, 601803 (4), Somatic mosaicism"				
chr12	66793	178459	12p13.33	12p13.33		612118	"IQSEC3, KIAA1110"	IQ motif- and SEC7 domain-containing protein 3	IQSEC3	440073	ENSG00000120645			Iqsec3 (MGI:2677208)			
chr12	190076	214204	12p13	12p13.33		603080	SLC6A12	"Solute carrier family 6 (neurotransmitter transporter, betaine/GABA), member 12"	SLC6A12	6539	ENSG00000111181			Slc6a12 (MGI:95628)			
chr12	220620	262929	12p13.3	12p13.33		615097	"SLC6A13, GAT2, GAT3"	"Solute carrier family 6 (neurotransmitter transporter, GABA), member 13"	SLC6A13	6540	ENSG00000010379			Slc6a13 (MGI:95629)			
chr12	280056	389454	12p11	12p13.33		180202	"KDM5A, JARID1A, RBP2, RBBP2"	Lysine(K)-specific demethylase 5A	KDM5A	5927	ENSG00000073614			Kdm5a (MGI:2136980)			
chr12	460376	561891	12p13.3	12p13.33		612220	B4GALNT3	"Beta-1,4-N-acetylgalactosaminyltransferase 3"	B4GALNT3	283358	ENSG00000139044			B4galnt3 (MGI:3041155)			
chr12	564295	663740	12p13	12p13.33		607297	NINJ2	Nerve injury-induced protein 2	NINJ2	4815	ENSG00000171840			Ninj2 (MGI:1352751)			
chr12	752592	911451	12p13	12p13.33		605232	"WNK1, PRKWNK1, KDP, PHA2C, HSAN2, HSN2"	WNK lysine deficient protein kinase 1	WNK1	65125	ENSG00000060237		"Neuropathy, hereditary sensory and autonomic, type II, 201300 (3), Autosomal recessive; Pseudohypoaldosteronism, type IIC, 614492 (3), Autosomal dominant"	Wnk1 (MGI:2442092)			
chr12	911027	991194	12p13-p12.2	12p13.33		600392	RAD52	"RAD52, yeast, homolog of"	RAD52	5893	ENSG00000002016			Rad52 (MGI:101949)			
chr12	1529855	1647212	12p13.3	12p13.33		606361	WNT5B	"Wingless-type MMTV integration site family, member 5B"	WNT5B	81029	ENSG00000111186			Wnt5b (MGI:98959)			
chr12	1559640	1594189	12p13.33	12p13.33		609081	"FBXL14, FBL14"	F-box and leucine-rich repeat protein 14	FBXL14	144699	ENSG00000171823			Fbxl14 (MGI:2141676)			
chr12	1691026	1788678	12p13.31	12p13.33		607946	"ADIPOR2, FLJ21432"	Adiponectin receptor 2	ADIPOR2	79602	ENSG00000006831			Adipor2 (MGI:93830)			
chr12	1791956	1922605	12p13.3	12p13.33		608171	"CACNA2D4, RCD4"	"Calcium channel, voltage-dependent, alpha-2/delta subunit 4"	CACNA2D4	93589	ENSG00000151062		"Retinal cone dystrophy 4, 610478 (3), Autosomal recessive"	Cacna2d4 (MGI:2442632)			
chr12	1941590	2004534	12p13.33	12p13.33		609843	"DCP1B, DCP1"	"Decapping enzyme 1, S. cerevisiae, homolog of"	DCP1B	196513	ENSG00000151065			Dcp1b (MGI:2442404)			
chr12	1969551	2697948	12p13.3	12p13.33		114205	"CACNA1C, CACNL1A1, CCHL1A1, TS"	"Calcium channel, voltage-dependent, L type, alpha 1C subunit"	CACNA1C	775	ENSG00000151067		"Brugada syndrome 3, 611875 (3); Timothy syndrome, 601005 (3), Autosomal dominant"	Cacna1c (MGI:103013)			
chr12	2794941	2805422	12p13.33	12p13.33		600611	"FKBP4, FKBP52"	FK506-binding protein 4	FKBP4	2288	ENSG00000004478			Fkbp4 (MGI:95543)			
chr12	2812620	2859906	12p13.33	12p13.33		617421	"ITFG2, FGGAP1"	Integrin-alpha FG-GAP repeat-containing protein 2	ITFG2	55846	ENSG00000111203			Itfg2 (MGI:1915450)			
chr12	2857679	2877154	12p13	12p13.33		602341	"FOXM1, FKHL16, HFH11"	Forkhead box M1	FOXM1	2305	ENSG00000111206			Foxm1 (MGI:1347487)			
chr12	2876257	2889524	12p13.33	12p13.33		614085	"RHNO1, RHINO, C12orf32"	"Rad9-, Rad1-, and Hus1-interacting nuclear orphan 1"	RHNO1	83695	ENSG00000171792						
chr12	2890866	2941139	12p13	12p13.33		604730	TULP3	Tubby-like protein 3	TULP3	7289	ENSG00000078246			Tulp3 (MGI:1329045)			
chr12	2959311	3040675	12p13.3-p13.2	12p13.33		601714	"TEAD4, TCF13L1, RTEF1"	"TEA domain family, member 4"	TEAD4	7004	ENSG00000197905			Tead4 (MGI:106907)			
chr12	3077354	3286563	12p13.32	12p13.33-p13.32		613137	"TSPAN9, NET5"	Tetraspanin 9	TSPAN9	10867	ENSG00000011105			Tspan9 (MGI:1924558)			
chr12	3381348	3593972	12p13.3	12p13.32		610086	"PRMT8, HRMT1L3, HRMT1L4"	Protein arginine methyltransferase 8	PRMT8	56341	ENSG00000111218			Prmt8 (MGI:3043083)			
chr12	3613365	3753217	12p13.32	12p13.32		614178	"EFCAB4B, CRACR2A"	EF-hand calcium-binding domain-containing protein 4B	CRACR2A	84766	ENSG00000130038			Cracr2a (MGI:2685919)			
chr12	3808860	3873470	12p13.3	12p13.32		616706	"PARP11, ARTD11"	"Poly(ADP-ribose) polymerase family, member 11"	PARP11	57097	ENSG00000111224			Parp11 (MGI:2141505)			
chr12	4273735	4305355	12p13	12p13.32		123833	"CCND2, MPPH3"	Cyclin D2	CCND2	894	ENSG00000118971		"Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3, 615938 (3), Autosomal dominant"	Ccnd2 (MGI:88314)			
chr12	4321192	4360027	12p13.3	12p13.32		610775	"TIGAR, C12orf5"	TP53-induced glycolysis and apoptosis regulator	TIGAR	57103	ENSG00000078237			Tigar (MGI:2442752)			
chr12	4368226	4379727	12p13.3	12p13.32		605380	"FGF23, ADHR, HPDR2, PHPTC"	Fibroblast growth factor 23	FGF23	8074	ENSG00000118972		"Hypophosphatemic rickets, autosomal dominant, 193100 (3), Autosomal dominant; Osteomalacia, tumor-induced (1); Tumoral calcinosis, hyperphosphatemic, familial, 211900 (3), Autosomal recessive"	Fgf23 (MGI:1891427)			
chr12	4434141	4445798	12p13	12p13.32		134921	FGF6	Fibroblast growth factor-6	FGF6	2251	ENSG00000111241			Fgf6 (MGI:95520)			
chr12	4487729	4538507	12p13.3	12p13.32		616082	C12orf4	Chromosome 12 open reading frame 4	C12orf4	57102	ENSG00000047621			D6Wsu163e (MGI:107893)			
chr12	4538783	4560046	12p13.2-p13.1	12p13.32		603070	"RAD51AP1, PIR51"	Rad51-associated protein 1	RAD51AP1	10635	ENSG00000111247			Rad51ap1 (MGI:1098224)			
chr12	4590071	4613887	12p13.32	12p13.32		609181	DYRK4	Dual-specificity tyrosine phosphorylation-regulated kinase 4	DYRK4	8798	ENSG00000010219			Dyrk4 (MGI:1330292)			
chr12	4649097	4687553	12p	12p13.32		603834	NDUFA9	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 9"	NDUFA9	4704	ENSG00000139180		"Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufa9 (MGI:1913358)			
chr12	4720585	4772725	12p13.3	12p13.32		606250	GALNT8	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 8	GALNT8	26290	ENSG00000130035						
chr12	4806876	4851926	12p13	12p13.32		176257	KCNA6	"Potassium voltage-gated channel, shaker-related subfamily, member 6"	KCNA6	3742	ENSG00000130035			Kcna6 (MGI:96663)			
chr12	4909906	4918255	12p13	12p13.32		176260	"KCNA1, AEMK, EA1"	"Potassium voltage-gated channel, shaker-related subfamily, member 1"	KCNA1	3736	ENSG00000111262	close to VWF	"Episodic ataxia/myokymia syndrome, 160120 (3), Autosomal dominant"	Kcna1 (MGI:96654)			
chr12	5043918	5046787	12p13	12p13.32		176267	"KCNA5, ATFB7"	"Potassium voltage-gated channel, shaker-related subfamily, member 5"	KCNA5	3741	ENSG00000130037		"Atrial fibrillation, familial, 7, 612240 (3), Autosomal dominant"	Kcna5 (MGI:96662)			
chr12	5432113	5495298	12p13	12p13.31		162660	NTF3	Neurotrophin-3	NTF3	4908	ENSG00000185652			Ntf3 (MGI:97380)			
chr12	5560240	5948789	12p13	12p13.31		610109	"ANO2, TMEM16B, C12orf3"	Anoctamin 2	ANO2	57101	ENSG00000047617			Ano2 (MGI:2387214)			
chr12	5948873	6124674	12p13.3	12p13.31		613160	"VWF, F8VWF"	Coagulation factor VIII VWF (von Willebrand factor)	VWF	7450	ENSG00000110799	pseudogene on chr. 22	"von Willebrand disease, type 1, 193400 (3), Autosomal dominant; von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3), Autosomal recessive, Autosomal dominant; von Willibrand disease, type 3, 277480 (3), Autosomal recessive"	Vwf (MGI:98941)			
chr12	6199706	6238270	12p13	12p13.31		143030	"CD9, MIC3"	CD9 antigen (p24)	CD9	928	ENSG00000010278			Cd9 (MGI:88348)			
chr12	6310435	6328505	12p13.31	12p13.31		611743	"PLEKHG6, MYOGEF"	"Pleckstrin homology domain-containing protein, family G, member 6"	PLEKHG6	55200	ENSG00000008323			Plekhg6 (MGI:2682298)			
chr12	6328756	6342116	12p13.2	12p13.31		191190	"TNFRSF1A, TNFR1, TNFAR, FPF, MS5"	"Tumor necrosis factor receptor superfamily, member 1A"	TNFRSF1A	7132	ENSG00000067182		"{Multiple sclerosis, susceptibility to, 5}, 614810 (3); Periodic fever, familial, 142680 (3), Autosomal dominant"	Tnfrsf1a (MGI:1314884)			
chr12	6346842	6377356	12p13	12p13.31		600228	"SCNN1A, BESC2"	"Sodium channel, nonvoltage-gated 1, alpha"	SCNN1A	6337	ENSG00000111319		"Bronchiectasis with or without elevated sweat chloride 2, 613021 (3), Autosomal dominant; Pseudohypoaldosteronism, type I, 264350 (3), Autosomal recessive"	Scnn1a (MGI:101782)			
chr12	6375367	6391570	12p13	12p13.31		600979	"LTBR, TNFCR"	Lymphotoxin-beta receptor (tumor necrosis factor C receptor)	LTBR	4055	ENSG00000111321	tightly linked to TNFR1 in mouse		Ltbr (MGI:104875)			
chr12	6444866	6451717	12p13	12p13.31		186711	"CD27, TNFRSF7, S152. LPFS2"	CD27 antigen	CD27	939	ENSG00000139193		"Lymphoproliferative syndrome 2, 615122 (3), Autosomal recessive"	Cd27 (MGI:88326)			
chr12	6451655	6472005	12p13.3	12p13.31		607081	TAPBPR	TAP-binding protein-related protein	TAPBPL	55080	ENSG00000139192			Tapbpl (MGI:2384853)			
chr12	6462236	6470898	12p13.31	12p13.31		185880	"VAMP1, SYB1, SPAX1"	Vesicle-associated membrane protein-1 (synaptobrevin-1)	VAMP1	6843	ENSG00000139190		"Spastic ataxia 1, autosomal dominant, 108600 (3), Autosomal dominant"	Vamp1 (MGI:1313276)			
chr12	6492149	6493304	12p13.3-p13.1	12p13.31		611855	"MRPL51, MRP64"	Mitochondrial ribosomal protein L51	MRPL51	51258	ENSG00000111639			Mrpl51 (MGI:1913743)			
chr12	6494131	6531965	12p13.31	12p13.31		615638	"NCAPD2, CNAP1, KIAA0159"	Non-SMC condensin I complex subunit D2	NCAPD2	9918	ENSG00000010292			Ncapd2 (MGI:1915548)			
chr12	6510221	6510550	12p13.31	12p13.31		615639	SCARNA10	Small cajal body-specific RNA 10	SCARNA10	692148		in intron 4 of NCAPD2					
chr12	6534516	6538374	12p13.31-p13.1	12p13.31		138400	"GAPDH, GAPD"	Glyceraldehyde-3-phosphate dehydrogenase	GAPDH	2597	ENSG00000111640	pseudogene on Xp21-q11		"Gapdh,Gapdh-ps15 (MGI:5434255,MGI:95640)"			
chr12	6539527	6556096	12p13.31	12p13.31		610495	IFFO1	Intermediate filament family orphan 1	IFFO1	25900	ENSG00000010295			Iffo1 (MGI:2444516)			
chr12	6556869	6568331	12p13	12p13.31		164031	NOL1	"Nucleolar protein 1, 120kD"	NOP2	4839	ENSG00000111641			Nop2 (MGI:107891)			
chr12	6570081	6607438	12p13	12p13.31		603277	"CHD4, SIHIWES"	Chromodomain helicase DNA-binding protein-4	CHD4	1108	ENSG00000111642		"Sifrim-Hitz-Weiss syndrome, 617159 (3), Autosomal dominant"	Chd4 (MGI:1344380)			
chr12	6618834	6636130	12p13	12p13.31		606926	"LPAR5, GPR92, GPR93, LPA5"	Lysophosphatidic acid receptor 5	LPAR5	57121	ENSG00000184574			Lpar5 (MGI:2685918)			
chr12	6650537	6663142	12p13.31	12p13.31		608524	ING4	Inhibitor of growth-4	ING4	51147	ENSG00000111653			Ing4 (MGI:107307)			
chr12	6666476	6689571	12p12	12p13.31		609951	"ZNF384, CIZ, CAGH1, NMP4"	Zinc finger protein 384	ZNF384	171017	ENSG00000126746			Zfp384 (MGI:2443203)			
chr12	6689704	6700842	12p13.31	12p13.31		616065	"PIANP, PANP, LEDA1"	PILR-alpha-associated neural protein	PIANP	196500	ENSG00000139200			Pianp (MGI:2441908)			
chr12	6723983	6731874	12p13.31	12p13.31		616009	"COPS7A, CSN7"	"COP9 signalosome, subunit 7A"	COPS7A	50813	ENSG00000111652			Cops7a (MGI:1349400)			
chr12	6747991	6753469	12p13	12p13.31		601401	MLF2	Myeloid leukemia factor-2	MLF2	8079	ENSG00000089693			Mlf2 (MGI:1353554)			
chr12	6766316	6770951	12p13.31	12p13.31		168440	PTMS	Parathymosin	PTMS	5763	ENSG00000159335	previously assigned to 17q12-q22					
chr12	6772482	6778454	12p13.32	12p13.31		153337	LAG3	Lymphocyte activation gene-3	LAG3	3902	ENSG00000089692			Lag3 (MGI:106588)			
chr12	6789471	6820809	12p13.31	12p13.31		186940	CD4	CD4 antigen (p55)	CD4	920	ENSG00000010610	CD = \'cluster of differentiation\' = nomenclature of leukocyte differentiation antigens	"OKT4 epitope deficiency, 613949 (3)"	Cd4 (MGI:88335)			
chr12	6828372	6839853	12p13	12p13.31		610342	"P3H3, LEPREL2"	Prolyl 3-hydroxylase 3	P3H3	10536	ENSG00000110811			P3h3 (MGI:1315208)			
chr12	6840853	6847394	12p13	12p13.31		139130	"GNB3, CSNB1H"	"Guanine nucleotide-binding protein, beta polypeptide-3"	GNB3	2784	ENSG00000111664		"{Hypertension, essential, susceptibility to}, 145500 (3), Multifactorial; Night blindness, congenital stationary, type 1H, 617024 (3), Autosomal recessive"	Gnb3 (MGI:95785)			
chr12	6852120	6866631	12p13	12p13.31		601447	"USP5, ISOT"	Ubiquitin-specific protease-5 (ubiquitin isopeptidase T)	USP5	8078	ENSG00000111667			Usp5 (MGI:1347343)			
chr12	6866833	6870945	12p13	12p13.31		190450	"TPI1, TPID"	Triosephosphate isomerase-1	TPI1	7167	ENSG00000111669		"Hemolytic anemia due to triosephosphate isomerase deficiency, 615512 (3), Autosomal recessive"	Tpi1 (MGI:98797)			
chr12	6870934	6873356	12p13.31	12p13.31		611658	"SPSB2, SSB2"	SPRY domain- and SOCS box-containing 2	SPSB2	84727	ENSG00000111671			Spsb2 (MGI:1315199)			
chr12	6914449	6923695	12p13	12p13.31		131360	ENO2	"Enolase-2, gamma, neuronal"	ENO2	2026	ENSG00000111674			Eno2 (MGI:95394)			
chr12	6924462	6942320	12p13.31	12p13.31		607462	"ATN1, DRPLA, HRS, NOD"	Atrophin 1	ATN1	1822	ENSG00000111676		"Dentatorubro-pallidoluysian atrophy, 125370 (3), Autosomal dominant"	Atn1 (MGI:104725)			
chr12	6943437	6946002	12p13	12p13.31		615140	"C12orf57, C10, TEMTYS"	Chromosome 12 open reading frame 57	C12orf57	113246	ENSG00000111678		"Temtamy syndrome, 218340 (3), Autosomal recessive"	Grcc10 (MGI:1315201)			
chr12	6943815	6943877	12p13.31	12p13.31		617876	"RNU7-1, RNU7"	"RNA, U7 small nuclear, 1"	RNU7-1	100147744							
chr12	6946576	6961315	12p13	12p13.31		176883	PTPN6	"Protein tyrosine phosphatase, nonreceptor-type, 6"	PTPN6	5777	ENSG00000111679			Ptpn6 (MGI:96055)			
chr12	6963698	6963765	12p13.31	12p13.31		612092	"MIR200C, MIRN200C"	Micro RNA 200C	MIR200C	406985							
chr12	6964096	6964190	12p13.31	12p13.31		612093	"MIR141, MIRN141"	Micro RNA 141	MIR141	406933							
chr12	6965351	6970752	12p13	12p13.31		610704	"PHB2, REA"	Prohibitin 2	PHB2	11331	ENSG00000215021			Phb2 (MGI:102520)			
chr12	6967336	6967605	12p13.31	12p13.31		615642	SCARNA12	Small Cajal body-specific RNA 12	SCARNA12	677777							
chr12	6970780	6997427	12p13	12p13.31		611531	"EMG1, NEP1, C2F, BWCNS"	"Essential for mitotic growth 1, S. cerevisiae, homolog of"	EMG1	10436	ENSG00000126749		"Bowen-Conradi syndrome, 211180 (3), Autosomal recessive"	Emg1 (MGI:1315195)			
chr12	6976184	7018537	12p13.31	12p13.31		611950	"LPCAT3, MBOAT5, NESSY"	Lysophosphatidylcholine acyltransferase 3	LPCAT3	10162	ENSG00000111684			Lpcat3 (MGI:1315211)			
chr12	7060660	7071031	12p13	12p13.31		120580	"C1S, EDSPD2"	"Complement component-1, s subcomponent"	C1S	716	ENSG00000182326		"C1s deficiency, 613783 (3); Ehlers-Danlos syndrome, periodontal type, 2, 617174 (3), Autosomal dominant"	"C1s2,C1s1 (MGI:1355312,MGI:3644269)"			
chr12	7080208	7092606	12p13	12p13.31		613785	"C1R, EDSPD1"	"Complement component-1, r subcomponent"	C1R	715	ENSG00000159403		"Ehlers-Danlos syndrome, periodontal type, 1, 130080 (3), Autosomal dominant"	"C1rb,C1ra (MGI:3779804,MGI:1355313)"			
chr12	7094549	7109277	12p13.31	12p13.31		608974	"C1RL, CLSPA, C1RLP"	Complement component C1r-like protein	C1RL	51279	ENSG00000139178			C1rl (MGI:2660692)			
chr12	7119105	7130271	12p13.31	12p13.31		611866	"RBP5, CRBP3"	Retinol-binding protein 5	RBP5	83758	ENSG00000139194						
chr12	7130370	7158944	12p13	12p13.31		611324	"CLSTN3, KIAA0726"	Calsyntenin 3	CLSTN3	9746	ENSG00000139182			Clstn3 (MGI:2178323)			
chr12	7188684	7218573	12p13.3	12p13.31		600414	"PEX5, PXR1, PTS1R, PBD2A, PBD2B, RCDP5"	Peroxisome biogenesis factor 5	PEX5	5830	ENSG00000139197		"Peroxisome biogenesis disorder 2A (Zellweger), 214110 (3), Autosomal recessive; Peroxisome biogenesis disorder 2B, 202370 (3), Autosomal recessive; Rhizomelic chondrodysplasia punctata, type 5, 616716 (3), Autosomal recessive"	Pex5 (MGI:1098808)			
chr12	7304331	7328372	12p13.31	12p13.31		614360	ACSM4	"Acyl-CoA synthetase medium-chain family, member 4"	ACSM4	341392	ENSG00000215009			Acsm4 (MGI:2681844)			
chr12	7320509	7444184	12p13.3	12p13.31		606079	"CD164L1, CD163B, M160"	CD164 antigen-like 1	CD163L1	283316	ENSG00000177675						
chr12	7470810	7503817	12p13.3	12p13.31		605545	CD163	CD163 antigen (hemoglobin scavenger receptor)	CD163	9332	ENSG00000177575			Cd163 (MGI:2135946)			
chr12	7649399	7670598	12p13.1	12p13.31		600130	"APOBEC1, BEDP"	"Apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1"	APOBEC1	339	ENSG00000111701			Apobec1 (MGI:103298)			
chr12	7689781	7695792	12p13.1	12p13.31		606522	"GDF3, KFS3, MCOPCB6, MCOP7"	Growth differentiation factor 3	GDF3	9573	ENSG00000184344		"Klippel-Feil syndrome 3, autosomal dominant, 613702 (3); Microphthalmia with coloboma 6, 613703 (3), Autosomal dominant; Microphthalmia, isolated 7, 613704 (3), Autosomal dominant"	Gdf3 (MGI:95686)			
chr12	7711453	7717558	12p13.31	12p13.31		608408	DPPA3	Developmental pluripotency-associated gene 3	DPPA3	359787	ENSG00000187569						
chr12	7729244	7751599	12p13.2-p12.3	12p13.31		606677	"CLEC4C, CLECSF11, DLEC, BDCA2"	"C-type lectin domain family 4, member C"	CLEC4C	170482	ENSG00000198178			Clec4b1 (MGI:1917060)			
chr12	7789395	7796060	12p13.31	12p13.31		607937	NANOG	Homeobox transcription factor NANOG	NANOG	79923	ENSG00000111704			Nanog (MGI:1919200)			
chr12	7812511	7891195	12p13.3	12p13.31		611039	"SLC2A14, GLUT14"	"Solute carrier family 2 (facilitated glucose transporter), member 14"	SLC2A14	144195	ENSG00000173262						
chr12	7919227	7936295	12p13.3	12p13.31		138170	"SLC2A3, GLUT3"	"Solute carrier family 2 (facilitated glucose transporter), member 3"	SLC2A3	6515	ENSG00000059804	pseudogene SLC2A3P on 5q34		Slc2a3 (MGI:95757)			
chr12	8056843	8066470	12p13.31	12p13.31		605246	"C3AR1, C3AR"	Complement component 3a receptor 1	C3AR1	719	ENSG00000171860			C3ar1 (MGI:1097680)			
chr12	8082210	8097776	12p13.31	12p13.31		611623	"NECAP1, EIEE21"	NECAP endocytosis-associated protein 1	NECAP1	25977	ENSG00000089818	mutation identified in 1 EIEE21 family	"?Epileptic encephalopathy, early infantile, 21, 615833 (3), Autosomal recessive"	Necap1 (MGI:1914852)			
chr12	8102901	8138606	12p13	12p13.31		605306	"CLEC4A, CLECSF6, DCIR, DDB27"	"C-type lectin domain family 4, member A"	CLEC4A	50856	ENSG00000111729			Clec4a2 (MGI:1349412)			
chr12	8221259	8227617	12p13.31	12p13.31		613041	FAM90A1	"Family with sequence similarity 90, member A1"	FAM90A1	55138	ENSG00000171847	other family members on chr. 8		Fam90a1b (MGI:1921682)			
chr12	8455994	8478329	12p13.31-p31.2	12p13.31		613579	"CLEC6A, CLEC4N"	"C-type lectin domain family 6, member A"	CLEC6A	93978	ENSG00000205846			Clec4n (MGI:1861231)			
chr12	8513491	8522365	12p13	12p13.31		609964	"CLEC4D, CLECSF8, CLEC6"	"C-type lectin domain family 4, member D"	CLEC4D	338339	ENSG00000166527			Clec4d (MGI:1298389)			
chr12	8533304	8541326	12p13	12p13.31		609962	"CLEC4E, MINCLE"	"C-type lectin domain family 4, member E"	CLEC4E	26253	ENSG00000166523			Clec4e (MGI:1861232)			
chr12	8602165	8612969	12p13	12p13.31		605257	"AICDA, AID, HIGM2"	Activation-induced cytidine deaminase	AICDA	57379	ENSG00000111732		"Immunodeficiency with hyper-IgM, type 2, 605258 (3), Autosomal recessive"	Aicda (MGI:1342279)			
chr12	8645942	8662887	12p13.1-p12.3	12p13.31		601103	"MFAP5, MAGP2, AAT9"	Microfibril-associated protein 5	MFAP5	8076	ENSG00000197614		"Aortic aneurysm, familial thoracic 9, 616166 (3), Autosomal dominant"	Mfap5 (MGI:1354387)			
chr12	8681676	8783097	12p13.31	12p13.31		614054	"RIMKLB, NAAGS"	"Ribosomal modification protein RimK-like family, member B"	RIMKLB	57494	ENSG00000166532			Rimklb (MGI:1918325)			
chr12	8822471	8887201	12p13.31	12p13.31		610627	A2ML1	Alpha-2-macroglobulin-like 1	A2ML1	144568	ENSG00000166535						
chr12	8914663	8941466	12p13.31	12p13.31		602978	"PHC1, EDR1, HPH1, RAE28, MCPH11"	Polyhomeotic-like 1	PHC1	1911	ENSG00000111752	mutations identified in 1 family	"?Microcephaly 11, primary, autosomal recessive, 615414 (3), Autosomal recessive"	Phc1 (MGI:103248)			
chr12	8940360	8949760	12p13	12p13.31		154540	M6PR	"Mannose-6-phosphate receptor, cation-dependent"	M6PR	4074	ENSG00000003056			M6pr (MGI:96904)			
chr12	8950043	9215656	12p13.31	12p13.31		604874	"KLRG1, MAFA, MAFAL"	"Killer cell lectin-like receptor, subfamily G, member 1"	KLRG1	10219	ENSG00000139187			Klrg1 (MGI:1355294)			
chr12	9067707	9116228	12p13.3-p12.3	12p13.31		103950	"A2M , A2MD"	Alpha-2-macroglobulin	A2M	2	ENSG00000175899	cluster of genes	"Alpha-2-macroglobulin deficiency, 614036 (1), Autosomal dominant; {Alzheimer disease, susceptibility to}, 104300 (3), Autosomal dominant"	A2m (MGI:2449119)			
chr12	9140729	9208369	12p13-p12.2	12p13.31		176420	PZP	Pregnancy zone protein	PZP	5858	ENSG00000126838						
chr12	9417690	9448171	12p13	12p13.31		601151	"DDX12, CHLR2"	DEAD/H box-12	DDX12P	440081							
chr12	9595273	9607900	12p13-p12	12p13.31		602890	"KLRB1, NKRP1A"	"Killer cell lectin-like receptor, subfamily B, member 1"	KLRB1	3820	ENSG00000111796			"Klrb1b,Klrb1c,Klrb1a (MGI:107538,MGI:107539,MGI:107540)"			
chr12	9669707	9699554	12p13	12p13.31		605659	"CLEC2D, LLT1"	"C-type lectin domain family 2, member D"	CLEC2D	29121	ENSG00000069493						
chr12	9715859	9733434	12p13.31	12p13.31		607467	"CLECL1, DCAL1"	C-type lectin-like 1	CLECL1	160365	ENSG00000184293						
chr12	9752485	9760900	12p13-p12	12p13.31		107273	CD69	"CD69 antigen (p60, early T-cell activation antigen)"	CD69	969	ENSG00000110848			Cd69 (MGI:88343)			
chr12	9827302	9845004	12p13.2-p12.3	12p13.31		605029	KLRF1	"Killer cell lectin-like receptor, subfamily F, member 1"	KLRF1	51348	ENSG00000150045						
chr12	9852368	9869858	12p13-p12	12p13.31		603242	"CLEC2B, CLECSF2, AICL"	"C-type lectin domain family 2, member B"	CLEC2B	9976	ENSG00000110852						
chr12	9882732	9932429	12p13.31	12p13.31		612087	CLEC2A	"C-type lectin domain family 2, member A"	CLEC2A	387836	ENSG00000188393			Clec2f (MGI:3522133)			
chr12	9951315	9995208	12p13	12p13.31		612088	"CLEC12A, MICL"	"C-type lectin domain family 12, member A"	CLEC12A	160364	ENSG00000172322			Clec12a (MGI:3040968)			
chr12	9986118	10001893	12p13	12p13.3-p13.2		606783	"CLEC2B, CLEC2"	"C-type lectin domain family 1, member B"	CLEC1B	51266	ENSG00000165682			Clec1b (MGI:1913287)			
chr12	10000000	27600000	12p13.2-p11.23			610143	DFNB62	"Deafness, autosomal recessive 62"	DFNB62	692220		between D12S358 and D12S1042	"Deafness, autosomal recessive 62, 610143 (2), Autosomal recessive"				
chr12	10000000	113900000	12p13.2-q24.1			601458	IBD2	Inflammatory bowel disease 2	IBD2	3378		mainly ulcerative colitis	"{Inflammatory bowel disease 2}, 601458 (2)"				
chr12	10000000	12600000	12p13.2			168710	PCS	Parotid proline-rich salivary protein Pc				linked to PRB2					
chr12	10000000	12600000	12p13.2			613967	"TAS2R45, T2R45"	"Taste receptor, type 2, member 45"	TAS2R45	259291	ENSG00000255374						
chr12	10006137	10018799	12p13.2	12p13.2		617573	CLEC12B	"C-type lectin domain family 12, member B"	CLEC12B	387837	ENSG00000256660			Clec12b (MGI:1918433)			
chr12	10030676	10066029	12p13.31	12p13.2		612252	"CLEC9A, DNGR1"	"C-type lectin domain family 9, member A"	CLEC9A	283420	ENSG00000197992			Clec9a (MGI:2444608)			
chr12	10069503	10099064	12p13	12p13.2		606782	"CLEC1A, CLEC1"	"C-type lectin domain family 1, member A"	CLEC1A	51267	ENSG00000150048			Clec1a (MGI:2444151)			
chr12	10116776	10130268	12p13.2-p12.3	12p13.2		606264	"CLEC7A, CLECSF12, DECTIN1, CANDF4"	"C-type lectin domain family 7, member A"	CLEC7A	64581	ENSG00000172243	in natural killer gene complex	"{Aspergillosis, susceptibility to}, 614079 (3); Candidiasis, familial, 4, autosomal recessive, 613108 (3), Autosomal recessive"	Clec7a (MGI:1861431)			
chr12	10158299	10172190	12p13-p12	12p13.2		602601	"OLR1, LOX1"	"Low density lipoprotein, oxidized, receptor 1"	OLR1	4973	ENSG00000173391		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Olr1 (MGI:1261434)			
chr12	10212845	10223127	12p12.3	12p13.2		607420	"GABARAPL1, GEC1"	GABA-A receptor-associated protein-like protein 1	GABARAPL1	23710	ENSG00000139112			Gabarapl1 (MGI:1914980)			
chr12	10238382	10329606	12p13.2-p12.3	12p13.2		602894	"KLRD1, CD94"	"Killer cell lectin-like receptor, subfamily D, member 1"	KLRD1	3824	ENSG00000134539			Klrd1 (MGI:1196275)			
chr12	10372352	10390053	12p13.2-p12.3	12p13.2		611817	"KLRK1, NKG2D"	"Kill cell lectin-like receptor, subfamily K, member 1"	KLRK1	22914	ENSG00000213809						
chr12	10407383	10409756	12p13.2-p12.3	12p13.2		602893	"KLRC4, NKG2F, D12S2489E"	"Killer cell lectin-like receptor, subfamily C, member 4"	KLRC4	8302	ENSG00000183542						
chr12	10412314	10420594	12p13.2-p12.3	12p13.2		602892	"KLRC3, NKG2E"	"Killer cell lectin-like receptor, subfamily C, member 3"	KLRC3	3823	ENSG00000205810						
chr12	10430598	10435992	12p13.2-p12.3	12p13.2		602891	"KLRC2, NKG2C"	"Killer cell lectin-like receptor, subfamily C, member 2"	KLRC2	3822	ENSG00000205809						
chr12	10441672	10454684	12p13.2-p12.3	12p13.2		161555	"KLRC1, NKG2, NKG2A"	"Killer cell lectin-like receptor, subfamily C, member 1"	KLRC1	3821	ENSG00000134545	family of at least 3 genes on 12		Klrc1 (MGI:1336161)			
chr12	10588477	10599834	12p13-p12	12p13.2		604274	"KLRA1, LY49L"	"Killer cell lectin-like receptor, subfamily A, member 1"	KLRA1P	10748		?functional					
chr12	10618922	10674317	12p13.2	12p13.2		611433	"STYK1, NOK"	Serine/threonine/tyrosine kinase 1	STYK1	55359	ENSG00000060140			Styk1 (MGI:2141396)			
chr12	10699076	10723441	12p13.1	12p13.2		603437	"CSDA, DBPA"	Cold-shock domain protein A	YBX3	8531	ENSG00000060138			Ybx3 (MGI:2137670)			
chr12	10801531	10802626	12p13	12p13.2		604793	"TRB4, T2R7"	"Taste receptor, family B, member 4"	TAS2R7	50837	ENSG00000121377			Tas2r130 (MGI:2681278)			
chr12	10806050	10806979	12p13	12p13.2		604794	"TRB5, T2R8"	"Taste receptor, family B, member 5"	TAS2R8	50836	ENSG00000121314						
chr12	10809093	10810167	12p13	12p13.2		604795	"TRB6, T2R9"	"Taste receptor, family B, member 6"	TAS2R9	50835	ENSG00000121381						
chr12	10825345	10826268	12p13	12p13.2		604791	"TRB2, T2R10"	"Taste receptor, family B, member 2"	TAS2R10	50839	ENSG00000121318			Tas2r114 (MGI:2681218)			
chr12	10845848	10849475	Chr.12	12p13.2		605359	"PROL4, LPRP"	"Proline rich 4, lacrimal"	PRR4	11272	ENSG00000111215						
chr12	10880960	11171622	12p13.2	12p13.2		168730	PRH1	"Proline-rich protein HaeIII, subfamily-1"	PRH1	5554	ENSG00000231887	"Pa, Db, PIF alleles"					
chr12	10907925	10909561	12p13	12p13.2		604792	"TRB3, T2R13"	"Taste receptor, family B, member 3"	TAS2R13	50838	ENSG00000212128			Tas2r121 (MGI:2681259)			
chr12	10929235	10934844	12p13.2	12p13.2		168790	PRH2	"Proline-rich protein HaeIII, subfamily-2"	PRH2	5555	ENSG00000134551	Pr allele					
chr12	10938253	10939206	12p13	12p13.2		604790	"TRB1, T2R14"	"Taste receptor, family B, member 1"	TAS2R14	50840	ENSG00000212127			Tas2r140 (MGI:2681298)			
chr12	10985912	10986911	12p13.2	12p13.2		609627	"TAS2R50, T2R50, TAS2R51, T2R51"	"Taste receptor, type 2, member 50"	TAS2R50	259296	ENSG00000212126						
chr12	10995961	10998303	12p13.2	12p13.2		613962	"TAS2R20, T2R56"	"Taste receptor, type 2, member 20"	TAS2R20	259295	ENSG00000255837						
chr12	11021618	11022619	12p13	12p13.2		613961	"TAS2R19, T2R19, T2R48"	"Taste receptor, type 2, member 19"	TAS2R19	259294	ENSG00000212124						
chr12	11030386	11031406	12p13.2	12p13.2		612669	"TAS2R31, TAS2R44, T2R53"	"Taste receptor, type 2, member 31"	TAS2R31	259290	ENSG00000256436			Tas2r136 (MGI:2681304)			
chr12	11061364	11062293	12p13.2	12p13.2		612774	"TAS2R46, T2R46, T2R54"	"Taste receptor, type 2, member 46"	TAS2R46	259292	ENSG00000226761			Tas2r120 (MGI:2681256)			
chr12	11091286	11092312	12p13.2	12p13.2		612668	"TAS2R43, T2R52"	"Taste receptor, type 2, member 43"	TAS2R43	259289	ENSG00000255374						
chr12	11133284	11134243	12p13.2	12p13.2		613963	"TAS2R30, T2R30, T2R47"	"Taste receptor, type 2, member 30"	TAS2R30	259293	ENSG00000256188	previously assigned to chr.1					
chr12	11185992	11186936	12p13	12p13.2		613966	"TAS2R42, T2R42, T2R55"	"Taste receptor, type 2, member 42"	TAS2R42	353164	ENSG00000186136			Tas2r131 (MGI:2681280)			
chr12	11265913	11269706	12p13.2	12p13.2		168840	PRB3	"Proline-rich protein BstNI, subfamily-3 (parotid salivary glycoprotein)"	PRB3	5544	ENSG00000197870	G1 allele					
chr12	11307080	11310434	12p13.2	12p13.2		180990	PRB4	"Proline-rich protein BstNI, subfamily-4"	PRB4	5545	ENSG00000230657	"Po, CON1, CON2 alleles"					
chr12	11351822	11355589	12p13.2	12p13.2		180989	PRB1	"Proline-rich protein BstNI, subfamily-1"	PRB1	5542	ENSG00000251655						
chr12	11391539	11395563	12p13.2	12p13.2		168810	PRB2	"Proline-rich protein BstNI, subfamily-2 (parotid size variant)"	PRB2	653247	ENSG00000121335	Ps allele					
chr12	11649600	11895401	12p13	12p13.2		600618	"ETV6, TEL, THC5"	ETS variant gene-6 (TEL oncogene)	ETV6	2120	ENSG00000139083	fused to PDGFRB or AML1 in leukemia	"Leukemia, acute myeloid, somatic, 601626 (3); Thrombocytopenia 5, 616216 (3), Autosomal dominant"	Etv6 (MGI:109336)			
chr12	12049843	12099694	12p12	12p13.2		606126	BCLG	Apoptosis regulator BCLG	BCL2L14	79370	ENSG00000121380			Bcl2l14 (MGI:1914063)			
chr12	12116024	12267021	12p13.3-p11.2	12p13.2		603507	"LRP6, ADCAD2, STHAG7"	Low density lipoprotein receptor-related protein 6	LRP6	4040	ENSG00000070018		"{Coronary artery disease, autosomal dominant, 2}, 610947 (3), Autosomal dominant; Tooth agenesis, selective, 7, 616724 (3), Autosomal dominant"	Lrp6 (MGI:1298218)			
chr12	12357077	12471220	12p13.2	12p13.2		616598	"BORCS5, LOH12CR1, MYRLYSIN"	"BLOC1-related complex, subunit 5"	BORCS5	118426	ENSG00000165714			Borcs5 (MGI:1915024)			
chr12	12473281	12562513	12p12	12p13.2		607175	"DUSP16, MKP7, KIAA1700"	Dual-specificity phosphatase 16	DUSP16	80824	ENSG00000111266			Dusp16 (MGI:1917936)			
chr12	12611832	12645107	12p13	12p13.1		603476	CREBL2	Cyclic AMP response element-binding protein-like 2	CREBL2	1389	ENSG00000111269			Crebl2 (MGI:1889385)			
chr12	12659690	12717785	12p13.2-p12.3	12p13.1		602927	GPR19	G protein-coupled receptor-19	GPR19	2842	ENSG00000183150			Gpr19 (MGI:892973)			
chr12	12717269	12722382	12p13	12p13.1		600778	"CDKN1B, KIP1, CDKN4, MEN4"	"Cyclin-dependent kinase inhibitor 1B (p27, Kip1)"	CDKN1B	1027	ENSG00000111276		"Multiple endocrine neoplasia, type IV, 610755 (3), Autosomal dominant"	Cdkn1b (MGI:104565)			
chr12	12725916	12791465	12p13.2	12p13.1		612456	"APOLD1, VERGE"	Apolipoprotein L domain-containing 1	APOLD1	81575	ENSG00000178878			Apold1 (MGI:2685921)			
chr12	12813345	12829980	12p13.1	12p13.1		615428	DDX47	DEAD box polypeptide 47	DDX47	51202	ENSG00000213782			Ddx47 (MGI:1915005)			
chr12	12891021	12913665	12p13.1	12p13.1		604138	"GPRC5A, RAI3, RAIG1"	"G protein-coupled receptor, family C, group 5, member A"	GPRC5A	9052	ENSG00000013588			Gprc5a (MGI:1891250)			
chr12	12940517	12955907	12p13.3	12p13.1		607437	GPRC5D	"G protein-coupled receptor, family C, group 5, member D"	GPRC5D	55507	ENSG00000111291			Gprc5d (MGI:1935037)			
chr12	12974863	13000308	Chr.12	12p13.1		605826	"HEBP1, HBP"	Heme-binding protein 1	HEBP1	50865	ENSG00000013583			Hebp1 (MGI:1333880)			
chr12	13044380	13083448	12p13.1	12p13.1		617838	"FAM234B, KIAA1467"	"Family with sequence similarity 234, member B"	FAM234B	57613	ENSG00000084444			Fam234b (MGI:1921775)			
chr12	13196667	13216773	12p12.3	12p13.1		602333	"EMP1, TMP"	Epithelial membrane protein-1	EMP1	2012	ENSG00000134531			Emp1 (MGI:107941)			
chr12	13537336	13982011	12p12	12p13.1		138252	"GRIN2B, NMDAR2B, MRD6, EIEE27"	"Glutamate receptor, ionotropic, N-methyl D-aspartate 2B"	GRIN2B	2904	ENSG00000273079		"Epileptic encephalopathy, early infantile, 27, 616139 (3), Autosomal dominant; Mental retardation, autosomal dominant 6, 613970 (3), Autosomal dominant"	Grin2b (MGI:95821)			
chr12	14254913	14255485	12p13.1	12p13.1		139180	"GNAI2P1, GNAI2L, GNAI2A"	"Guanine nucleotide-binding protein (G protein), alpha-inhibiting, polypeptide 2 pseudogene 1"	GNAI2P1	2772							
chr12	14365631	14502934	12p13.1	12p13.1		613644	"ATF7IP, AM, MCAF, MCAF1"	Activating transcription factor 7-interacting protein	ATF7IP	55729	ENSG00000171681			Atf7ip (MGI:1858965)			
chr12	14612631	14696624	12p12	12p12.3		601330	"GUCY2C, GUC2C, DIAR6, MECIL"	Guanylate cyclase 2C (heat stable enterotoxin receptor)	GUCY2C	2984	ENSG00000070019		"Diarrhea 6, 614616 (3), Autosomal dominant; Meconium ileus, 614665 (3), Autosomal recessive"	Gucy2c (MGI:106903)			
chr12	14770719	14771130	12p13.1	12p12.3		615069	HIST4H4	"Histone gene cluster 4, H4 histone"	HIST4H4	121504	ENSG00000197837			Hist1h4i (MGI:2448432)			
chr12	14825568	14843532	12p13-p12	12p12.3		110600	"ART4, DO, DOK1"	ADP-ribosyltransferase-4 (Dombrock blood group)	ART4	420	ENSG00000111339		"[Blood group, Dombrock], 616060 (3)"	Art4 (MGI:1202710)			
chr12	14880863	14886061	12p13.1-p12.3	12p12.3		154870	MGP	Matrix Gla protein	MGP	4256	ENSG00000111341		"Keutel syndrome, 245150 (3), Autosomal recessive"	Mgp (MGI:96976)			
chr12	14942014	14961769	12p12.3	12p12.3		602843	"ARHGDIB, GDID4, D4"	Rho GDP dissociation inhibitor (GDI) beta	ARHGDIB	397	ENSG00000111348			Arhgdib (MGI:101940)			
chr12	14973021	14981864	12p13	12p12.3		601190	"PDE6H, RCD3, ACHM6"	"Phosphodiesterase 6H, cGMP-specific, cone, gamma"	PDE6H	5149	ENSG00000139053		"Achromatopsia 6, 610024 (3), Autosomal recessive, Autosomal dominant; Retinal cone dystrophy 3, 610024 (3), Autosomal recessive, Autosomal dominant"	Pde6h (MGI:1925850)			
chr12	15107781	15221476	12p12	12p12.3		612664	RERG	Ras-like and estrogen-regulated growth inhibitor	RERG	85004	ENSG00000134533			Rerg (MGI:2665139)			
chr12	15322256	15598330	12p13-p12	12p12.3		600579	"PTPRO, GLEPP1, NPHS6"	"Protein tyrosine phosphatase, receptor type, O"	PTPRO	5800	ENSG00000151490		"Nephrotic syndrome, type 6, 614196 (3), Autosomal recessive"	Ptpro (MGI:1097152)			
chr12	15620140	15789575	12p12.3	12p12.3		600206	"EPS8, DFNB102"	Epidermal growth factor receptor pathway substrate-8	EPS8	2059	ENSG00000151491	mutation identified in 1 DFNB102 family	"?Deafness, autosomal recessive 102, 615974 (3), Autosomal recessive"	Eps8 (MGI:104684)			
chr12	15882353	15903477	12p12.3	12p12.3		605986	"STRAP, UNRIP, MAWD"	Serine/threonine kinase receptor-associated protein	STRAP	11171	ENSG00000023734	previously assigned to 12q		Strap (MGI:1329037)			
chr12	16347141	16377188	Chr.12	12p12.3		138330	"MGST1, GST12"	Microsomal glutathione S-transferase 1	MGST1	4257	ENSG00000008394	pseudogene at 12q13-q14		Mgst1 (MGI:1913850)			
chr12	16548371	16610232	12p13	12p12.3		180386	"LMO3, RBTNL2, RHOM3"	LIM domain only 3 (rhombotin-like 2)	LMO3	55885	ENSG00000048540	expressed mainly in brain					
chr12	16988746	16990627	12p12	12p12.3		601435	"SKP1P2, SKP1B"	S-phase kinase-associated protein 1 pseudogene 2 (p19B)	SKP1P2	728622							
chr12	18242945	18716860	12p12	12p12.3		609001	PIK3C2G	"Phosphatidylinositol 3-kinase, class 2, gamma"	PIK3C2G	5288	ENSG00000139144			Pik3c2g (MGI:1203730)			
chr12	18645528	18738058	12p12.3	12p12.3		608075	"PLCZ1, SPGF17"	"Phospholipase C, zeta-1"	PLCZ1	89869	ENSG00000139151	mutation identified in 1 SPGF17 family	"?Spermatogenic failure 17, 617214 (3), Autosomal recessive"	Plcz1 (MGI:2150308)			
chr12	18738110	18739187	12p12	12p12.3		608722	"CAPZA3, CAPPA3"	"Capping protein, actin, alpha-3"	CAPZA3	93661	ENSG00000177938			Capza3 (MGI:106221)			
chr12	19129679	19376399	12p12	12p12.3		607770	"PEPP2, KIAA1686"	Phosphatidylinositol 3-phosphate-binding PH domain protein 2	PLEKHA5	54477	ENSG00000052126			Plekha5 (MGI:1923802)			
chr12	19800000	26300000	12p12.2-p12.1			608742	HYT4	"Hypertension, essential, susceptibility to, 4"		444980			"{Hypertension, essential, susceptibility to, 4}, 145500 (2), Multifactorial"				
chr12	20369244	20688578	12p12.2	12p12.2		123805	"PDE3A, HTNB"	"Phosphodiesterase 3A, cGMP-inhibited"	PDE3A	5139	ENSG00000172572		"Hypertension and brachydactyly syndrome, 112410 (3), Autosomal dominant"	Pde3a (MGI:1860764)			
chr12	20681799	20753385	12p12	12p12.2		613389	"SLCO1C1, OATPF, OATP14, SLC21A14"	"Solute carrier organic anion transporter family, member 1C1"	SLCO1C1	53919	ENSG00000139155			Slco1c1 (MGI:1889679)			
chr12	20810703	20916910	12p12.2	12p12.2		605495	"SLCO1B3, OATP8, OATP1B3, SLC21A8, HBLRR"	"Solute carrier organic anion transporter family, member 1B3"	SLCO1B3	28234	ENSG00000111700	HBLRR digenic with SLCO1B1	"Hyperbilirubinemia, Rotor type, digenic, 237450 (3), Digenic recessive"	Slco1b2 (MGI:1351899)			
chr12	21131193	21239795	12p12	12p12.1		604843	"SLCO1B1, LST1, OATP2, OATPC, OATP1B1, HBLRR"	"Solute carrier organic anion transporter family, member 1B1"	SLCO1B1	10599	ENSG00000134538	HBLRR digenic with SLCO1B3	"Hyperbilirubinemia, Rotor type, digenic, 237450 (3), Digenic recessive"				
chr12	21264599	21403662	12p12	12p12.1		602883	"SLC21A3, OATP"	"Solute carrier family 21 (organic anion transporter), member 3"	SLCO1A2	6579	ENSG00000084453			Slco1a5 (MGI:1351865)			
chr12	21354959	21379979	12p12.3-p12.1	12p12.1		147940	IAPP	Islet amyloid polypeptide (diabetes-associated peptide; amylin)	IAPP	3375	ENSG00000121351			Iapp (MGI:96382)			
chr12	21437603	21471251	12p12.1	12p12.1		617220	"PYROXD1, MFM8"	Pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1	PYROXD1	79912	ENSG00000121350		"Myopathy, myofibrillar, 8, 617258 (3), Autosomal recessive"	Pyroxd1 (MGI:2676395)			
chr12	21468909	21501668	12p12-p11	12p12.1		600537	"RECQL, RECQL1"	"RecQ helicase-like (DNA helicase, RecQ-like 1)"	RECQL	5965	ENSG00000004700			Recql (MGI:103021)			
chr12	21501175	21518402	12p12.1	12p12.1		615078	"GOLT1B, GOT1B, GCT2"	Golgi transport 1B	GOLT1B	51026	ENSG00000111711			Golt1b (MGI:1914214)			
chr12	21531526	21604857	12p12.2	12p12.1		138571	GYS2	"Glycogen synthase-2, liver"	GYS2	2998	ENSG00000111713		"Glycogen storage disease 0, liver, 240600 (3), Autosomal recessive"	Gys2 (MGI:2385254)			
chr12	21635341	21657970	12p12.2-p12.1	12p12.1		150100	"LDHB, LDHBD"	Lactate dehydrogenase B	LDHB	3945	ENSG00000111716		"[Lactate dehydrogenase-B deficiency], 614128 (3)"	Ldhb (MGI:96763)			
chr12	21764954	21775592	12p11.23	12p12.1		600935	KCNJ8	"Potassium inwardly-rectifying channel, subfamily J, member 8"	KCNJ8	3764	ENSG00000121361			Kcnj8 (MGI:1100508)			
chr12	21797388	21941862	12p12.1	12p12.1		601439	"ABCC9, SUR2, CMD1O, ATFB12, CANTU"	"ATP-binding cassette, subfamily C, member 9 (sulfonylurea receptor 2)"	ABCC9	10060	ENSG00000069431		"Atrial fibrillation, familial, 12, 614050 (3), Autosomal dominant; Cardiomyopathy, dilated, 1O, 608569 (3); Hypertrichotic osteochondrodysplasia, 239850 (3), Autosomal dominant"	Abcc9 (MGI:1352630)			
chr12	22046173	22065673	12p12.1	12p12.1		603316	CMAS	Cytidine monophosphate N-acetylneuraminic acid synthetase	CMAS	55907	ENSG00000111726			Cmas (MGI:1337124)			
chr12	22193390	22334713	12p12.1-p11.2	12p12.1		601123	SIAT8	"Sialyltransferase-8 (alpha-N-acetylneuraminate: alpha-2,8-sialyltransferase, GD3 synthase)"	ST8SIA1	6489	ENSG00000111728			St8sia1 (MGI:106011)			
chr12	22625141	22690673	12p12.1-p11.2	12p12.1		609858	"ETNK1, EKI1"	Ethanolamine kinase 1	ETNK1	55500	ENSG00000139163			Etnk1 (MGI:1922570)			
chr12	23529498	24562700	12p12.1	12p12.1		604975	"SOX5, LAMSHF"	SRY-box 5	SOX5	6660	ENSG00000134532	some LAMSHF patients have 12p12 deletions	"Lamb-Shaffer syndrome, 616803 (3), Autosomal dominant"	Sox5 (MGI:98367)			
chr12	24810023	24949458	12p12	12p12.1		113520	"BCAT1, BCT1"	"Branched chain aminotransferase-1, cytosolic"	BCAT1	586	ENSG00000060982		?Hyperleucinemia-isoleucinemia or hypervalinemia (1)	Bcat1 (MGI:104861)			
chr12	24917701	24918383	12p12.1-p11.2	12p12.1		609860	DADR	DAD1-related gene	DAD1P1	56286							
chr12	25052100	25108334	12p12.1	12p12.1		602003	"LRMP, JAW1"	Lymphoid-restricted membrane protein	LRMP	4033	ENSG00000118308			Lrmp (MGI:108424)			
chr12	25107056	25195161	12p12.1	12p12.1		616906	"CASC1, LAS1, PPP1R54"	Cancer susceptibility candidate 1	CASC1	55259	ENSG00000118307			Casc1 (MGI:2444480)			
chr12	25204788	25251002	12p12.1	12p12.1		190070	"KRAS, KRAS2, RASK2, NS, CFC2, RALD"	Kirsten rat sarcoma-2 viral (v-Ki-ras2) oncogene homolog	KRAS	3845	ENSG00000133703	pseudogene KRAS1P on 6p12-p11	"Arteriovenous malformation of the brain, somatic, 108010 (3); Bladder cancer, somatic, 109800 (3); Breast cancer, somatic, 114480 (3); Cardiofaciocutaneous syndrome 2, 615278 (3); Gastric cancer, somatic, 137215 (3); Leukemia, acute myeloid, 601626 (3), Autosomal dominant; Lung cancer, somatic, 211980 (3); Noonan syndrome 3, 609942 (3), Autosomal dominant; Pancreatic carcinoma, somatic, 260350 (3); RAS-associated autoimmune leukoproliferative disorder, 614470 (3), Autosomal dominant; Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200 (3)"	Kras (MGI:96680)			
chr12	25476081	25648603	12p12.1	12p12.1		617254	"LMNTD1, IFLTD1, LMNARS1, PAS1C1"	Lamin tail domain-containing protein 1	LMNTD1	160492	ENSG00000152936			Lmntd1 (MGI:1921321)			
chr12	25958231	26079891	12p12.1	12p12.1		608231	"RASSF8, C12orf2"	"RAS association domain family, member 8"	RASSF8	11228	ENSG00000123094			Rassf8 (MGI:1918573)			
chr12	26120025	26125069	12p12.1-p11.23	12p12.1		606200	"BHLHE41, BHLHB3, DEC2, SHARP1"	"Basic helix-loop-helix domain-containing protein, member E41"	BHLHE41	79365	ENSG00000123095		"[Short sleeper], 612975 (3), Autosomal dominant"				
chr12	26121950	26234776	12p11.2	12p12.1		601599	"SSPN, KRAG"	Sarcospan (Kirsten-ras associated gene)	SSPN	8082	ENSG00000123096			Sspn (MGI:1353511)			
chr12	26300000	51100000	12p11.23-q13.12			602096	AD5	"Alzheimer disease, familial, type 5"	AD5	8081			"Alzheimer disease-5, 602096 (2), Autosomal dominant"				
chr12	26300000	54500000	12p11.2-q13.1			615022	ARCI7	"Ichthyosis, congenital, autosomal recessive 7"		101202686		between D12S345 and D12S390	"Ichthyosis, congenital, autosomal recessive 7, 615022 (2), Autosomal recessive"				
chr12	26300000	67300000	12p11.2-q14			606257	STQTL3	Stature quantitative trait locus 3		282549		max lod at D12S398 and D12S10990	"{Stature QTL 3}, 606257 (2)"				
chr12	26300000	57700000	12p11-q13			615390	VUR7	Vesicoureteral reflux 7		102095631		max lod at D12S1048	"Vesicoureteral reflux 7, 615390 (2)"				
chr12	26335336	26833197	12p11	12p11.23		600144	"ITPR2, ANHD"	"Inositol 1,4,5-triphosphate receptor, type 2"	ITPR2	3709	ENSG00000123104	mutation has been identified in 1 ANHD family	"?Anhidrosis, isolated, with normal sweat glands, 106190 (3), Autosomal recessive"	Itpr2 (MGI:99418)			
chr12	26905170	26938337	12p11.23	12p11.23		615079	"ASUN, MAT89BB, GCT1"	"Asunder, spermatogenesis regulator"	INTS13	55726	ENSG00000064102			Ints13 (MGI:1918427)			
chr12	26966523	27014426	12q11-q12	12p11.23		605181	TM7SF3	"Transmembrane 7 superfamily, member 3"	TM7SF3	51768	ENSG00000064115			Tm7sf3 (MGI:1914873)			
chr12	27022521	27030672	12p11.23	12p11.23		603800	"MED21, SURB7, SRB7"	Mediator complex subunit 21	MED21	9412	ENSG00000152944			Med21 (MGI:1347064)			
chr12	27244144	27325958	12p12.3	12p11.23		615836	"STK38L, NDR2, KIAA0965"	Serine/threonine protein kinase 38-like protein	STK38L	23012	ENSG00000211455			Stk38l (MGI:1922250)			
chr12	27332853	27425812	12p11.23	12p11.23		614517	"ARNTL2, BMAL2, CLIF"	Aryl hydrocarbon receptor nuclear translocator-like protein 2	ARNTL2	56938	ENSG00000029153			Arntl2 (MGI:2684845)			
chr12	27696518	27697595	12p11.22	12p11.22		610848	REP15	Rab15 effector protein	REP15	387849	ENSG00000174236			Rep15 (MGI:1913782)			
chr12	27710772	27756303	12q21.1-q21.3	12p11.22		611995	"MRPS35, MRPS28"	Mitochondrial ribosomal protein S35	MRPS35	60488	ENSG00000061794	3 pseudogenes		Mrps35 (MGI:2385255)			
chr12	27958083	27972863	12p12.1-p11.2	12p11.22		168470	"PTHLH, BDE2"	Parathyroid hormone-like hormone	PTHLH	5744	ENSG00000087494		"Brachydactyly, type E2, 613382 (3), Autosomal dominant; Humoral hypercalcemia of malignancy (1)"	Pthlh (MGI:97800)			
chr12	28190426	28550165	12p11.22	12p11.22		617366	CCDC91	Coiled-coil domain-containing protein 91	CCDC91	55297	ENSG00000123106			Ccdc91 (MGI:1914265)			
chr12	29149002	29335616	12p11.23	12p11.22		616156	"FAR2, MLSTD1"	Fatty acyl CoA reductase 2	FAR2	55711	ENSG00000064763			Far2 (MGI:2687035)			
chr12	29336543	29381209	12p11.22	12p11.22		612236	"ERGIC2, CDA14, PTX1"	Endoplasmic reticulum-golgi intermediate compartment protein 2	ERGIC2	51290	ENSG00000087502			Ergic2 (MGI:1914706)			
chr12	29500812	29784758	12p11.22	12p11.22		615855	TMTC1	Transmembrane and tetratricopeptide repeat domains-containing protein 1	TMTC1	83857	ENSG00000133687			Tmtc1 (MGI:3039590)			
chr12	30628980	30695994	12p11.2	12p11.21		605600	"IPO8, RANBP8"	Importin 8	IPO8	10526	ENSG00000133704			Ipo8 (MGI:2444611)			
chr12	30709551	30754992	12p11.21	12p11.21		610375	"CAPRIN2, C1QDC1, EEG1, KIAA1873"	"Caprin family, member 2"	CAPRIN2	65981	ENSG00000110888			Caprin2 (MGI:2448541)			
chr12	31073844	31104798	12p11	12p11.21		601150	"DDX11, CHLR1, KRG2"	DEAD/H box-11 (CHL1-related helicase gene-1)	DDX11	1663	ENSG00000013573		"Warsaw breakage syndrome, 613398 (3), Autosomal recessive"	Ddx11 (MGI:2443590)			
chr12	31280583	31326224	12p11	12p11.21		615027	"SINHCAF, FAM60A"	SIN3-HDAC complex associated factor	SINHCAF	58516	ENSG00000139146			Fam60a (MGI:1929091)			
chr12	31382222	31591017	12p11.21	12p11.21		617279	DENND5B	DENN domain-containing protein 5B	DENND5B	160518	ENSG00000170456			Dennd5b (MGI:2444273)			
chr12	31647159	31673113	12p11.21	12p11.21		615256	"ETFBKMT, METTL20, C12orf72"	Electron transfer flavoprotein beta-subunit lysine methyltransferase	ETFBKMT	254013	ENSG00000139160			Etfbkmt (MGI:2443575)			
chr12	31791184	31792240	12p11.21	12p11.21		616134	H3F3C	"H3 histone, family 3C"	H3F3C	440093	ENSG00000188375			Gm12657 (MGI:3651714)			
chr12	32106772	32383636	12p11.2-p11.1	12p11.21		602204	BICD1	"Bicaudal-D, Drosophila, homolog of, 1"	BICD1	636	ENSG00000151746	second homolog on 9q		Bicd1 (MGI:1101760)			
chr12	32399522	32646049	12p11.2	12p11.21		611104	"FGD4, FRABIN, CMT4H"	"FYVE, RhoGEF, and PH domain-containing protein 4"	FGD4	121512	ENSG00000139132		"Charcot-Marie-Tooth disease, type 4H, 609311 (3), Autosomal recessive"	Fgd4 (MGI:2183747)			
chr12	32679199	32745649	12p11.21	12p11.21		603850	"DNM1L, DRP1, DVLP, DYMPLE, EMPF1, OPA5"	Dynamin 1-like	DNM1L	10059	ENSG00000087470		"Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1, 614388 (3), Autosomal recessive, Autosomal dominant; Optic atrophy 5, 610708 (3), Autosomal dominant"	Dnm1l (MGI:1921256)			
chr12	32725246	32756457	12p11.21	12p11.21		610957	"YARS2, TYRRS, MLASA2"	Tyrosyl-tRNA synthetase 2	YARS2	51067	ENSG00000139131		"Myopathy, lactic acidosis, and sideroblastic anemia 2, 613561 (3), Autosomal recessive"	Yars2 (MGI:1917370)			
chr12	32790745	32896845	12p11	12p11.21		602861	"PKP2, ARVD9"	Plakophilin-2	PKP2	5318	ENSG00000057294	pseudogene on 12p13	"Arrhythmogenic right ventricular dysplasia 9, 609040 (3), Autosomal dominant"	Pkp2 (MGI:1914701)			
chr12	34022280	34035295	12p11.1	12p11.1		603313	"ALG10, KCR1"	"Alg10, S. cerevisiae, homolog of"	ALG10	84920	ENSG00000139133		"{Long QT syndrome, acquired, reduced susceptibility to}, 613688 (3), Autosomal dominant"	Alg10b (MGI:2146159)			
chr12	35500000	133275309	12q			179010	"IHPS1, IHPS"	"Pyloric stenosis, infantile hypertrophic 1"					"Pyloric stenosis, infantile hypertrophic 1, 179010 (2), Autosomal dominant, Multifactorial"				
chr12	37800000	92200000	12q12-q21			102300	RLS1	"Restless legs syndrome, susceptibility to, 1"		192142		between D12S1044 and D12S78	"{Restless legs syndrome 1}, 102300 (2), Autosomal dominant"				
chr12	39293227	39443389	12q12	12q12		608283	"KIF21A, KIAA1708, FEOM1, CFEOM1, CFEOM3B"	Kinesin family member 21A	KIF21A	55605	ENSG00000139116		"Fibrosis of extraocular muscles, congenital, 1, 135700 (3), Autosomal dominant; Fibrosis of extraocular muscles, congenital, 3B, 135700 (3), Autosomal dominant"	Kif21a (MGI:109188)			
chr12	39530964	39651332	12q11-q12	12q12		601081	"ABCD2, ALDR, ALDL1"	"ATP-binding cassette, subfamily D, member 2"	ABCD2	225	ENSG00000173208			Abcd2 (MGI:1349467)			
chr12	39755020	40106084	12q12	12q12		611036	"SLC2A13, HMIT"	"Solute carrier family 2 (facilitated glucose transporter), member 13"	SLC2A13	114134	ENSG00000151229			Slc2a13 (MGI:2146030)			
chr12	40224889	40369284	12q12	12q12		609007	"LRRK2, PARK8"	Leucine-rich repeat kinase 2 (dardarin)	LRRK2	120892	ENSG00000188906		"{Parkinson disease 8}, 607060 (3), Autosomal dominant"	Lrrk2 (MGI:1913975)			
chr12	40393393	40570756	12q12	12q12		612170	MUC19	"Mucin 19, oligomeric"	MUC19	283463							
chr12	40692428	41072411	12q11-q12	12q12		600016	"CNTN1, MYPCN"	Contactin 1	CNTN1	1272	ENSG00000018236	mutation identified in 1 MYPCN family	"?Myopathy, congenital, Compton-North, 612540 (3), Autosomal recessive"	Cntn1 (MGI:105980)			
chr12	41188447	41574589	12q12	12q12		609730	PDZRN4	PDZ domain-containing ring finger protein 4	PDZRN4	29951	ENSG00000165966			Pdzrn4 (MGI:3056996)			
chr12	42081844	42144870	12q12	12q12		613321	"GXYLT1, GLT8D3"	Glucoside xylosyltransferase 1	GXYLT1	283464	ENSG00000151233			Gxylt1 (MGI:2684933)			
chr12	42157103	42238372	12q12	12q12		607534	YAF2	YY1-associated factor 2	YAF2	10138	ENSG00000015153						
chr12	42312085	42326129	12q12	12q12		610750	"ZCRB1, MADP1"	Zinc finger CCHC domain- and RNA-binding motif-containing protein 1	ZCRB1	85437	ENSG00000139168	"possible pseudogenes on chr16, X, and 6"		Zcrb1 (MGI:1914447)			
chr12	42326125	42448620	12q12	12q12		608150	PPHLN1	Periphilin 1	PPHLN1	51535	ENSG00000134283			Pphln1 (MGI:1917029)			
chr12	42458337	42589769	12q12	12q12		608500	"PRICKLE1, RILP, EPM1B"	Prickle-like 1	PRICKLE1	144165	ENSG00000139174		"Epilepsy, progressive myoclonic 1B, 612437 (3), Autosomal recessive"	Prickle1 (MGI:1916034)			
chr12	43352842	43551970	12q11	12q12		611681	ADAMTS20	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 20"	ADAMTS20	80070	ENSG00000173157			Adamts20 (MGI:2660628)			
chr12	43758908	43789542	12q12	12q12		606883	"IRAK4, REN64, IPD1"	Interleukin 1 receptor-associated kinase 4	IRAK4	51135	ENSG00000198001		"IRAK4 deficiency, 607676 (3); Invasive pneumococcal disease, recurrent isolated, 1, 610799 (3)"	Irak4 (MGI:2182474)			
chr12	43793722	43806374	12q12	12q12		610932	"TWF1, PTK9"	"Twinfilin, Drosophila, homolog of, 1"	TWF1	5756	ENSG00000151239			Twf1 (MGI:1100520)			
chr12	44508274	44921847	12q13.11-q13.12	12q12		602320	NELL2	Nel-like 2	NELL2	4753	ENSG00000184613			Nell2 (MGI:1858510)			
chr12	45215986	45440403	12q12	12q12		608663	"ANO6, TMEM16F, SCTS, BDPLT7"	Anoctamin 6	ANO6	196527	ENSG00000177119		"Scott syndrome, 262890 (3), Autosomal recessive"	Ano6 (MGI:2145890)			
chr12	45729705	45908039	12q12	12q12		609539	"ARID2, BAF200, KIAA1557, CSS6"	AT-rich interaction domain-containing protein 2	ARID2	196528	ENSG00000189079		"Coffin-Siris syndrome 6, 617808 (3), Autosomal dominant"	Arid2 (MGI:1924294)			
chr12	45919130	45992039	12q12-q13.11	12q12		603668	"SCAF11, SFRS2IP, SIP1, CASP11, SRRP129"	SR-related C-terminal domain-associated factor 11	SCAF11	9169	ENSG00000139218	previously assigned to 21q22.3		Scaf11 (MGI:1919443)			
chr12	46000000	57700000	12q13			613061	BCC4	"Basal cell carcinoma, susceptibility to, 4"		100307121		associated with rs11170164	"{Basal cell carcinoma, susceptibility to, 4}, 613061 (2)"				
chr12	46000000	57700000	12q13			616182	CMTS	"Chronic mountain sickness, susceptibility to"		105180377			"{Chronic mountain sickness, susceptibility to}, 616182 (2)"				
chr12	46000000	67300000	12q13-q14			607841	DFNA48	"Deafness, autosomal dominant 48"					"Deafness, autosomal dominant 48, 607841 (2), Autosomal dominant"				
chr12	46000000	92200000	12q13-q21			600808	ENUR2	"Enuresis, nocturnal, 2"	ENUR2	2032			"Enuresis, nocturnal, 2, 600808 (2), Autosomal dominant"				
chr12	46000000	57700000	12q13			167960	HPV18I2	Human papillomavirus type 18 integration site-2	HPV18I2	3261		on 8 near MYC in HeLa					
chr12	46000000	71100000	12q13.11-q15			614346	MRT25	"Mental retardation, autosomal recessive 25"	MRT25	100852403		between rs4760658 and rs1882033	"Mental retardation, autosomal recessive 25, 614346 (2), Autosomal recessive"				
chr12	46000000	67300000	12q13-q14			604681	PABPL2	Poly(A)-binding protein-like 2				?pseudogenes on 3q and 13q					
chr12	46000000	57700000	12q13			184100	SPDT	"Spondyloepiphyseal dysplasia tarda, autosomal dominant"		103875461			"Spondyloepiphyseal dysplasia tarda, autosomal dominant, 184100 (2), Autosomal dominant"				
chr12	46183054	46269424	12q13.11	12q13.11		608490	SLC38A1	"Solute carrier family 38 (amino acid transporter), member 1"	SLC38A1	81539	ENSG00000111371			Slc38a1 (MGI:2145895)			
chr12	46358187	46372861	12q13.11	12q13.11		605180	"SLC38A2, ATA2, KIAA1382"	"Solute carrier family 38, member 2"	SLC38A2	54407	ENSG00000134294			Slc38a2 (MGI:1915010)			
chr12	46764760	46832421	12q13	12q13.11		608065	"SLC38A4, NAT3, ATA3"	"Solute carrier family 38 (amino acid transporter), member 4"	SLC38A4	55089	ENSG00000139209			Slc38a4 (MGI:1916604)			
chr12	47075706	47080825	12q13.11	12q13.11		615690	"AMIGO2, ALI1"	Adhesion molecule with Ig-like domain 2	AMIGO2	347902	ENSG00000139211			Amigo2 (MGI:2145995)			
chr12	47661931	47706060	12q13.11	12q13.11		611477	RPAP3	RNA polymerase II-associated protein 3	RPAP3	79657	ENSG00000005175			Rpap3 (MGI:1277218)			
chr12	47709733	47725571	12q13.1	12q13.11		606720	"ENDOU, PP11"	Endonuclease polyU-specific	ENDOU	8909	ENSG00000111405			Endou (MGI:97746)			
chr12	47753618	47782752	12q13	12q13.11		612187	HRG1	Heme-responsive gene 1	SLC48A1	55652	ENSG00000211584			Slc48a1 (MGI:1914989)			
chr12	47734669	47759105	Chr.12	12q13.11		606057	EPAC	cAMP-regulated guanine nucleotide exchange factor I	RAPGEF3	10411	ENSG00000079337			Rapgef3 (MGI:2441741)			
chr12	47782709	47820611	Chr.12	12q13.11		606542	"HDAC7A, HDAC7"	Histone deacetylase 7A	HDAC7	51564	ENSG00000061273			Hdac7 (MGI:1891835)			
chr12	47841536	47905030	12q12-q14	12q13.11		601769	VDR	"Vitamin D (1,25-dihydroxyvitamin D3) receptor"	VDR	7421	ENSG00000111424		"?Osteoporosis, involutional, 166710 (1), Autosomal dominant; Rickets, vitamin D-resistant, type IIA, 277440 (3), Autosomal recessive"	Vdr (MGI:103076)			
chr12	47972964	48006211	12q13.11-q13.2	12q13.11		120140	COL2A1	"Collagen II, alpha-1 polypeptide"	COL2A1	1280	ENSG00000139219		"Achondrogenesis, type II or hypochondrogenesis, 200610 (3), Autosomal dominant; Avascular necrosis of the femoral head, 608805 (3), Autosomal dominant; Czech dysplasia, 609162 (3), Autosomal dominant; Epiphyseal dysplasia, multiple, with myopia and deafness, 132450 (3), Autosomal dominant; Kniest dysplasia, 156550 (3), Autosomal dominant; Legg-Calve-Perthes disease, 150600 (3), Autosomal dominant; Osteoarthritis with mild chondrodysplasia, 604864 (3), Autosomal dominant; Platyspondylic skeletal dysplasia, Torrance type, 151210 (3), Autosomal dominant; SED congenita, 183900 (3), Autosomal dominant; SMED Strudwick type, 184250 (3), Autosomal dominant; Spondyloepiphyseal dysplasia, Stanescu type, 616583 (3), Autosomal dominant; Spondyloperipheral dysplasia, 271700 (3), Autosomal dominant; Stickler sydrome, type I, nonsyndromic ocular, 609508 (3), Autosomal dominant; Stickler syndrome, type I, 108300 (3), Autosomal dominant; Vitreoretinopathy with phalangeal epiphyseal dysplasia (3)"	Col2a1 (MGI:88452)			
chr12	48042892	48106307	12q13.1	12q13.11		612157	SENP1	"Sentrin-specific protease family, member 1"	SENP1	29843	ENSG00000079387			Senp1 (MGI:2445054)			
chr12	48105252	48146403	12q13.3	12q13.11		610681	"PFKM, GSD7"	"Phosphofructokinase, muscle type"	PFKM	5213	ENSG00000152556	incorrectly assigned to chr.1	"Glycogen storage disease VII, 232800 (3), Autosomal recessive"	Pfkm (MGI:97548)			
chr12	48147787	48157594	12q13	12q13.11		615053	ASB8	Ankyrin repeat- and SOCS box-containing protein 8	ASB8	140461	ENSG00000177981			Asb8 (MGI:1925791)			
chr12	48334379	48351413	12q13.11	12q13.11		613906	ZNF641	Zinc finger protein 641	ZNF641	121274	ENSG00000167528			Zfp641 (MGI:2442788)			
chr12	48472664	48473059	12q13.11	12q13.11		606878	"ANP32D, PP32R2"	"Acidic leucine-rich nuclear phosphoprotein 32 family, member D"	ANP32D	23519	ENSG00000139223						
chr12	48567683	48571882	12q13	12q13.11		149750	LALBA	"Lactalbumin, alpha"	LALBA	3906	ENSG00000167531			Lalba (MGI:96742)			
chr12	48653210	48682251	12q13.11	12q13.11		615488	"KANSL2, NSL2, C12orf41"	"KAT8 regulatory NSL complex, subunit 2"	KANSL2	54934	ENSG00000139620			Kansl2 (MGI:1916862)			
chr12	48654381	48654517	12q13.11	12q13.11		615487	"SNORA2C, SNORA34, ACA34, MIR1291"	"Small nucleolar RNA, H/ACA box, 34"	SNORA2C	677815		MIR1291 in intron of SNORA34					
chr12	48688457	48716997	12q11-q13.3	12q13.11-q13.12		143055	"CCNT1, CCNT"	Cyclin T1	CCNT1	904	ENSG00000129315			Ccnt1 (MGI:1328363)			
chr12	48766190	48789095	12q12-q13	12q13.12		600294	"ADCY6, LCCS8"	Adenylate cyclase-6	ADCY6	112	ENSG00000174233	mutation identified in 1 LCCS8 family	"?Lethal congenital contracture syndrome 8, 616287 (3), Autosomal recessive"	Adcy6 (MGI:87917)			
chr12	48814431	48828942	12q13	12q13.12		601958	CACNB3	"Calcium channel, voltage-dependent, beta 3 subunit"	CACNB3	784	ENSG00000167535			Cacnb3 (MGI:103307)			
chr12	48829755	48852173	12q13.12	12q13.12		612172	"DDX23, PRP28"	Dead box polypeptide 23	DDX23	9416	ENSG00000174243			Ddx23 (MGI:1921601)			
chr12	48857132	48865869	12q13.12	12q13.12		609038	"RND1, RHO6"	Rho family GTPase 1	RND1	27289	ENSG00000172602			Rnd1 (MGI:2444878)			
chr12	48904109	48921575	12q13.12	12q13.12		611088	"CCDC65, CILD27"	Coiled-coil domain-containing protein 65	CCDC65	85478	ENSG00000139537		"Ciliary dyskinesia, primary, 27, 615504 (3), Autosomal recessive"	Ccdc65 (MGI:2146001)			
chr12	48921958	48925546	12q13	12q13.12		610571	"FKBP11, FKBP19"	FK506-binding protein 11	FKBP11	51303	ENSG00000134285			Fkbp11 (MGI:1913370)			
chr12	48930251	48957525	12q13	12q13.12		103190	ARF3	ADP-ribosylation factor-3	ARF3	377	ENSG00000134287			Arf3 (MGI:99432)			
chr12	48965339	48979586	12q13	12q13.12		601906	"WNT10B, SHFM6, STHAG8"	"Wingless-type MMTV integration site family, member 10B"	WNT10B	7480	ENSG00000169884		"Split-hand/foot malformation 6, 225300 (3), Autosomal recessive; Tooth agenesis, selective, 8, 617073 (3), Autosomal dominant"	Wnt10b (MGI:108061)			
chr12	48978452	48982612	12q12-q13	12q13.12		164820	"WNT1, INT1, OI15, BMND16"	"Wingless-type MMTV integration site family, member 1 (oncogene INT1)"	WNT1	7471	ENSG00000125084		"Osteogenesis imperfecta, type XV, 615220 (3), Autosomal recessive; {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, 615221 (3)"	Wnt1 (MGI:98953)			
chr12	48995148	49001772	12q13.1	12q13.12		610588	"DDN, KIAA0749"	Dendrin	DDN	23109	ENSG00000181418			Ddn (MGI:108101)			
chr12	49002271	49018974	12q13.1	12q13.12		602742	PRKAG1	"Protein kinase, AMP-activated, noncatalytic, gamma-1"	PRKAG1	5571	ENSG00000181929			Prkag1 (MGI:108411)			
chr12	49018974	49060883	12q13.12	12q13.12		602113	"KMT2D, MLL2, ALR, KABUK1"	Lysine (K)-specific methyltransferase 2D	KMT2D	8085	ENSG00000167548		"Kabuki syndrome 1, 147920 (3), Autosomal dominant"	Kmt2d (MGI:2682319)			
chr12	49086655	49094818	12q13.1	12q13.12		605423	"DHH, SRXY7, GDXYM"	Desert hedgehog	DHH	50846	ENSG00000139549		"46XY partial gonadal dysgenesis, with minifascicular neuropathy, 607080 (3); 46XY sex reversal 7, 233420 (3), Autosomal recessive"	Dhh (MGI:94891)			
chr12	49096550	49110899	12q13.12	12q13.12		610007	"LMBR1L, LIMR, KIAA1174"	Limb region 1 homolog-like	LMBR1L	55716	ENSG00000139636			Lmbr1l (MGI:1289247)			
chr12	49127781	49131520	12q13.12	12q13.12		602530	TUBA1B	"Tubulin, alpha-1B"	TUBA1B	10376	ENSG00000123416			Tuba1b (MGI:107804)			
chr12	49184794	49189323	12q12-q14	12q13.12		602529	"TUBA1A, TUBA3, LIS3"	"Tubulin, alpha-1A"	TUBA1A	7846	ENSG00000167552		"Lissencephaly 3, 611603 (3), Autosomal dominant"	Tuba1a (MGI:98869)			
chr12	49295125	49298697	12q12-q13	12q13.12		170710	PRPH	Peripherin	PRPH	5630	ENSG00000135406		"{Amyotrophic lateral sclerosis, susceptibility to}, 105400 (3), Autosomal recessive, Autosomal dominant"	Prph (MGI:97774)			
chr12	49332408	49337194	12q13	12q13.12		615229	"C1QL4, CTRP11"	"Complement component 1, q subcomponent-like 4"	C1QL4	338761	ENSG00000186897			C1ql4 (MGI:3579909)			
chr12	49366904	49527440	12q13.2	12q13.12		611667	"SPATS2, SPATA10, P59SCR, SCR59"	Spermatogenesis-associated serine-rich protein 2	SPATS2	65244	ENSG00000123352			Spats2 (MGI:1919822)			
chr12	49538540	49558311	12q13	12q13.12		604527	"KCNH3, BEC1"	"Potassium voltage-gated channel, subfamily H (eag-related), member 3"	KCNH3	23416	ENSG00000135519			Kcnh3 (MGI:1341723)			
chr12	49558293	49568232	12q13.12	12q13.12		609504	"MCRS1, MSP58, MCRS2"	"Microspherule protein 1 (microspherule protein 2, included)"	MCRS1	10445	ENSG00000187778			Mcrs1 (MGI:1858420)			
chr12	49636498	49707413	12q13	12q13.12		616288	"FMNL3, FRL2"	Formin-like 3	FMNL3	91010	ENSG00000161791			Fmnl3 (MGI:109569)			
chr12	49741509	49764933	12q13.12	12q13.12		600748	"TMBIM6, TEGT"	Transmembrane BAX inhibitor motif-containing protein 6	TMBIM6	7009	ENSG00000139644			Tmbim6 (MGI:99682)			
chr12	49791138	49828749	12q13.12	12q13.12		615104	"NCKAP5L, KIAA1602"	NCK-associated protein 5-like	NCKAP5L	57701	ENSG00000167566			Nckap5l (MGI:3609653)			
chr12	49866895	49903976	12q13	12q13.12		604306	"FAIM2, LFG, NMP35"	FAS apoptotic inhibitory molecule 2	FAIM2	23017	ENSG00000135472			Faim2 (MGI:1919643)			
chr12	49950740	49958880	12q13	12q13.12		107777	AQP2	Aquaporin-2 (collecting duct)	AQP2	359	ENSG00000167580		"Diabetes insipidus, nephrogenic, 125800 (3), Autosomal recessive, Autosomal dominant"	Aqp2 (MGI:1096865)			
chr12	49961495	49965681	12q13	12q13.12		600442	"AQP5, PPKB"	Aquaporin-5	AQP5	362	ENSG00000161798		"Palmoplantar keratoderma, Bothnian type, 600231 (3), Autosomal dominant"	Aqp5 (MGI:106215)			
chr12	49972836	49977138	12q13	12q13.12		601383	"AQP6, AQP2L"	"Aquaporin-6, kidney specific"	AQP6	363	ENSG00000086159			Aqp6 (MGI:1341204)			
chr12	49989161	50033205	12q13.12	12q13.12		604980	"RCGAP1, MGCRACGAP, CYK4"	"GTPase-activating protein, Rac, 1"	RACGAP1	29127	ENSG00000161800			Racgap1 (MGI:1349423)			
chr12	50057636	50083621	12q12	12q13.12		602866	ACCN2	"Cation channel, amiloride-sensitive, neuronal, 2"	ASIC1	41	ENSG00000110881			Asic1 (MGI:1194915)			
chr12	50085199	50100710	12q13-q14	12q13.12		601735	"SMARCD1, BAF60A"	"SW1/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1"	SMARCD1	6602	ENSG00000066117			Smarcd1 (MGI:1933623)			
chr12	50103818	50111319	12q12-q13	12q13.12		138420	"GPD1, HTGTI"	"Glycerol-3-phosphate dehydrogenase, soluble"	GPD1	2819	ENSG00000167588		"Hypertriglyceridemia, transient infantile, 614480 (3), Autosomal recessive"	Gpd1 (MGI:95679)			
chr12	50111980	50120456	12q13.12	12q13.12		614478	"COX14, C12orf62"	Cytochrome c oxidase assembly protein COX14	COX14	84987	ENSG00000178449	mutation identified in 1 Cox4 deficient family	"?Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Cox14 (MGI:1913629)			
chr12	50129305	50167532	12q13.12	12q13.12		615335	"CERS5, LASS5, TRH4"	Ceramide synthase 5	CERS5	91012	ENSG00000139624			Cers5 (MGI:1919199)			
chr12	50175779	50283569	12q13	12q13.12		608364	"LIMA1, EPLIN, SREBP3"	LIM domain and actin-binding protein 1	LIMA1	51474	ENSG00000050405			Lima1 (MGI:1920992)			
chr12	50504984	50748666	12q13.12	12q13.12		611379	"DIP2B, KIAA1463"	"Disco-interacting protein 2, Drosophila, homolog of, B"	DIP2B	57609	ENSG00000066084		"Mental retardation, FRA12A type, 136630 (3), Autosomal dominant"	Dip2b (MGI:2145977)			
chr12	50763681	50821161	12q13	12q13.12		123803	"ATF1, TREB36"	Activating transcription factor 1	ATF1	466	ENSG00000123268	"fused with EWS in soft tissue clear cell sarcoma, with FUS in angiomatoid fibrous histiocytoma"		"Atf1,Atf1-ps (MGI:3037720,MGI:1298366)"			
chr12	50952262	51028334	12q13	12q13.12		600523	"SLC11A2, NRAMP2, DCT1, DMT1, AHMIO1"	Solute carrier family 11 (proton-coupled divalent metal ion transporter) member 2	SLC11A2	4891	ENSG00000110911		"Anemia, hypochromic microcytic, with iron overload 1, 206100 (3), Autosomal recessive"	Slc11a2 (MGI:1345279)			
chr12	51093755	51173142	12q13	12q13.12-q13.13		189889	TFCP2	"Transcription factor CP2, alpha globin"	TFCP2	7024	ENSG00000135457			Tfcp2 (MGI:98509)			
chr12	51281037	51324679	12q13.13	12q13.13		605936	BIN2	Bridging integrator 2	BIN2	51411	ENSG00000110934	previously mapped to 4q22.1		Bin2 (MGI:3611448)			
chr12	51328442	51346678	12q13	12q13.13		130120	"CELA1, ELA1"	"Chymotrypsin-like elastase family, member 1"	CELA1	1990	ENSG00000139610	on proximal 12p		Cela1 (MGI:95314)			
chr12	51351869	51391954	12q13	12q13.13		605148	"GALNT6, GalNAcT6"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 6	GALNT6	11226	ENSG00000139629			Galnt6 (MGI:1891640)			
chr12	51391316	51515762	Chr.12	12q13.13		605024	"SLC4A8, NBC3"	"Solute carrier family 4 (sodium bicarbonate cotransporter), member 8"	SLC4A8	9498	ENSG00000050438			Slc4a8 (MGI:1928745)			
chr12	51589957	51812863	12q13	12q13.13		600702	"SCN8A, CIAT, EIEE13, BFIS5"	"Sodium channel, voltage gated, type VIII, alpha polypeptide"	SCN8A	6334	ENSG00000196876	mutation identified in 1 CIAT family	"?Cognitive impairment with or without cerebellar ataxia, 614306 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 13, 614558 (3), Autosomal dominant; Seizures, benign familial infantile, 5, 617080 (3), Autosomal dominant"	Scn8a (MGI:103169)			
chr12	51906912	51923360	12q11-q14	12q13.13		601284	"ACVRL1, ACVRLK1, ALK1, HHT2"	"Activin A receptor, type II-like kinase 1"	ACVRL1	94	ENSG00000139567		"Telangiectasia, hereditary hemorrhagic, type 2, 600376 (3), Autosomal dominant"	Acvrl1 (MGI:1338946)			
chr12	51951666	51997078	12q13	12q13.13		601300	"ACVR1B, ACVRLK4, ALK4"	"Activin A receptor, type IB"	ACVR1B	91	ENSG00000135503		"Pancreatic cancer, somatic (3)"	Acvr1b (MGI:1338944)			
chr12	52006944	52015888	12q13.13	12q13.13		612027	"GRASP, TAMALIN"	GRP1-associated scaffold protein	GRASP	160622	ENSG00000161835			Grasp (MGI:1860303)			
chr12	52022831	52059506	12q13	12q13.13		139139	"NR4A1, HMR, NP10, GFRP1"	"Nuclear receptor subfamily 4, group A, member 1"	NR4A1	3164	ENSG00000123358			Nr4a1 (MGI:1352454)			
chr12	52069922	52077494	12q13.13	12q13.13		615089	"ATG101, C12orf44"	Autophagy-related protein 101	ATG101	60673	ENSG00000123395			Atg101 (MGI:1915368)			
chr12	52168995	52191999	12q13.13	12q13.13		611161	"KRT80, KB20"	Keratin 80	KRT80	144501	ENSG00000167767			Krt80 (MGI:1921377)			
chr12	52233169	52252666	12q12-q14	12q13.13		148059	KRT7	Keratin 7	KRT7	3855	ENSG00000135480			Krt7 (MGI:96704)			
chr12	52270506	52309162	12q13	12q13.13		601928	"KRT86, KRTHB6, HB6"	Keratin 86	KRT86	3892	ENSG00000170442		"Monilethrix, 158000 (3), Autosomal dominant"	Krt86 (MGI:109362)			
chr12	52285912	52291514	12q13	12q13.13		602153	"KRT81, KRTHB1, HB1"	Keratin 81	KRT81	3887	ENSG00000205426		"Monilethrix, 158000 (3), Autosomal dominant"	Krt81 (MGI:1928858)			
chr12	52314300	52321397	12q13	12q13.13		602765	"KRT83, KRTHB3, HB3, MNLIX, EKVP5"	Keratin 83	KRT83	3889	ENSG00000170523		"Erythrokeratodermia variabilis et progressiva 5, 617756 (3), Autosomal recessive; Monilethrix, 158000 (3), Autosomal dominant"	Krt83 (MGI:3690448)			
chr12	52360005	52367524	12q13	12q13.13		602767	"KRT85, KRTHB5, HB5, ECTD4"	Keratin 85	KRT85	3891	ENSG00000135443		"Ectodermal dysplasia 4, hair/nail type, 602032 (3), Autosomal recessive"				
chr12	52377664	52386976	12q13.13	12q13.13		602766	"KRT84, KRTHB4, HB4"	Keratin 84	KRT84	3890	ENSG00000161849			Krt84 (MGI:96700)			
chr12	52393950	52406391	12q13.13	12q13.13		601078	"KRT82, KRTHB2, HB2"	Keratin 82	KRT82	3888	ENSG00000161850			Krt82 (MGI:2149248)			
chr12	52424069	52434325	12q13	12q13.13		609025	"KRT75, K6HF, PFB"	Keratin 75	KRT75	9119	ENSG00000170454		"{Pseudofolliculitis barbae, susceptibility to}, 612318 (3)"	Krt75 (MGI:1923500)			
chr12	52446650	52452125	12q13	12q13.13		148042	"KRT6B, PC4"	Keratin 6B	KRT6B	3854	ENSG00000185479		"Pachyonychia congenita 4, 615728 (3)"	"Krt6a,Krt6b (MGI:1333768,MGI:1100845)"			
chr12	52468515	52473784	12q13.13	12q13.13		612315	"KRT6C, PPKNEFD"	Keratin 6C	KRT6C	286887	ENSG00000170465		"Palmoplantar keratoderma, nonepidermolytic, focal or diffuse, 615735 (3), Autosomal dominant"				
chr12	52487173	52493396	12q13	12q13.13		148041	"KRT6A, PC3"	Keratin 6A	KRT6A	3853	ENSG00000205420		"Pachyonychia congenita 3, 615726 (3)"				
chr12	52514574	52520458	12q13	12q13.13		148040	"KRT5, DDD1"	Keratin 5	KRT5	3852	ENSG00000186081		"Dowling-Degos disease 1, 179850 (3), Autosomal dominant; Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3), Autosomal dominant; Epidermolysis bullosa simplex, Koebner type, 131900 (3), Autosomal dominant; Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3), Autosomal dominant; Epidermolysis bullosa simplex, recessive 1, 601001 (3), Autosomal recessive; Epidermolysis bullosa simplex-MCR, 609352 (3); Epidermolysis bullosa simplex-MP, 131960 (3), Autosomal dominant"	Krt5 (MGI:96702)			
chr12	52543908	52553146	12q13	12q13.13		608245	"KRT71, K6IRS1, KRT6IRS1, HYPT13"	Keratin 71	KRT71	112802	ENSG00000139648	mutation identified in 1 HYPT13 family	"?Hypotrichosis 13, 615896 (3), Autosomal dominant"	Krt71 (MGI:1861586)			
chr12	52565818	52573824	12q13	12q13.13		608248	"KRT74, K6IRS4, KRT6IRS4, HTSS2, HYPT3, ADWH"	Keratin 74	KRT74	121391	ENSG00000170484	mutation identified in 1 HYPT3 family and ECTD7 family	"?Ectodermal dysplasia 7, hair/nail type, 614929 (3), Autosomal recessive; ?Hypotrichosis 3, 613981 (3), Autosomal dominant; Woolly hair, autosomal dominant, 194300 (3), Autosomal dominant"				
chr12	52585588	52602899	12q13	12q13.13		608246	"KRT72, K6IRS2, KRT6IRS2"	Keratin 72	KRT72	140807	ENSG00000170486			Krt72 (MGI:2146034)			
chr12	52601812	52620132	12q13	12q13.13		608247	"KRT73, K6IRS3, KRT6IRS3"	Keratin 73	KRT73	319101	ENSG00000186049			Krt73 (MGI:3607712)			
chr12	52644557	52652174	12q11-q13	12q13.13		600194	"KRT2, KRT2A, KRT2E"	Keratin 2	KRT2	3849	ENSG00000172867		"Ichthyosis bullosa of Siemens, 146800 (3), Autosomal dominant"				
chr12	52674735	52680406	12q13	12q13.13		139350	"KRT1, EPPK, NEPPK, EHK"	Keratin 1	KRT1	3848	ENSG00000167768	close to Hox-3 in mouse; class II keratin	"Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive, Autosomal dominant; Ichthyosis histrix, Curth-Macklin type, 146590 (3), Autosomal dominant; Ichthyosis, cyclic, with epidermolytic hyperkeratosis, 607602 (3), Autosomal dominant; Keratosis palmoplantaris striata III, 607654 (3); Palmoplantar keratoderma, epidermolytic, 144200 (3), Autosomal dominant; Palmoplantar keratoderma, nonepidermolytic, 600962 (3), Autosomal dominant"	Krt1 (MGI:96698)			
chr12	52689611	52703523	12q13.13	12q13.13		611158	"KRT77, K1B"	Keratin 77	KRT77	374454	ENSG00000189182			Krt77 (MGI:3588209)			
chr12	52768154	52777344	12q13.13	12q13.13		616671	"KRT76, K76, KRT2P"	"Keratin 76, type II"	KRT76	51350	ENSG00000185069			Krt76 (MGI:1924305)			
chr12	52789684	52805734	12q13	12q13.13		148043	KRT3	Keratin 3	KRT3	3850	ENSG00000186442		"Meesmann corneal dystrophy, 122100 (3), Autosomal dominant"				
chr12	52806542	52814115	12q13	12q13.13		123940	"KRT4, CYK4, WSN1"	Keratin 4	KRT4	3851	ENSG00000170477	class II keratin	"White sponge nevus 1, 193900 (3), Autosomal dominant"	Krt4 (MGI:96701)			
chr12	52821446	52834292	12q13.13	12q13.13		611160	"KRT79,  KRT6L, K6L"	Keratin 79	KRT79	338785	ENSG00000185640			Krt79 (MGI:2385030)			
chr12	52837803	52848993	12q13.13	12q13.13		611159	"KRT78, K5B"	Keratin 78	KRT78	196374	ENSG00000170423			Krt78 (MGI:1917529)			
chr12	52897186	52949865	12q13	12q13.13		148060	KRT8	Keratin 8	KRT8	3856	ENSG00000170421		"Cirrhosis, cryptogenic, 215600 (3), Autosomal recessive; {Cirrhosis, noncryptogenic, susceptibility to}, 215600 (3), Autosomal recessive"	Krt8 (MGI:96705)			
chr12	52948870	52952900	12q13	12q13.13		148070	KRT18	Keratin 18	KRT18	3875	ENSG00000111057	"contiguous to KRT8, type II heteromer partner"	"Cirrhosis, cryptogenic, 215600 (3), Autosomal recessive; {Cirrhosis, noncryptogenic, susceptibility to}, 215600 (3), Autosomal recessive"	Krt18 (MGI:96692)			
chr12	53006257	53042214	12q13.13	12q13.13		603928	EIF4B	Eukaryotic translation initiation factor 4B	EIF4B	1975	ENSG00000063046			Eif4b (MGI:95304)			
chr12	53046979	53064378	12q13.13	12q13.13		607717	"TNS2, TENC1, C1TEN, KIAA1075"	Tensin 2	TNS2	23371	ENSG00000111077			Tns2 (MGI:2387586)			
chr12	53097651	53102343	Chr.12	12q13.13		146735	IGFBP6	Insulin-like growth factor-binding protein-6	IGFBP6	3489	ENSG00000167779			Igfbp6 (MGI:96441)			
chr12	53103489	53124538	12q13	12q13.13		601311	"SOAT2, ACACT2"	Sterol O-acyltransferase 2	SOAT2	8435	ENSG00000167780			Soat2 (MGI:1332226)			
chr12	53157662	53181662	12q13.13	12q13.13		616569	"CSAD, CSD, PCAP"	Cysteine sulfinic acid decarboxylase	CSAD	51380	ENSG00000139631			Csad (MGI:2180098)			
chr12	53191317	53207374	12q13.13	12q13.13		147559	ITGB7	"Integrin, beta-7"	ITGB7	3695	ENSG00000139626			Itgb7 (MGI:96616)			
chr12	53210565	53232255	12q13	12q13.13		180190	RARG	"Retinoic acid receptor, gamma polypeptide"	RARG	5916	ENSG00000172819			Rarg (MGI:97858)			
chr12	53268256	53293642	12q13	12q13.13		604143	"ESPL1, ESP1"	Extra spindle poles-like 1	ESPL1	9700	ENSG00000135476	prev. mapping to chr.8		Espl1 (MGI:2146156)			
chr12	53295450	53299449	12q12	12q13.13		604899	"PFDN5, MM1"	Prefoldin 5	PFDN5	5204	ENSG00000123349			Pfdn5 (MGI:1928753)			
chr12	53299685	53307180	12q13	12q13.13		611366	"C12orf10, MYG1"	Chromosome 12 open reading frame 10	C12orf10	60314	ENSG00000139637			Myg1 (MGI:1929864)			
chr12	53307455	53321627	12q13	12q13.13		605378	"AAAS, AAA"	Aladin	AAAS	8086	ENSG00000094914		"Achalasia-addisonianism-alacrimia syndrome, 231550 (3), Autosomal recessive"	Aaas (MGI:2443767)			
chr12	53326574	53344792	12q13.13	12q13.13		606633	"SP7, OSX, OI12"	Transcription factor Sp7	SP7	121340	ENSG00000170374	mutation identified in 1 OI12 patient	"?Osteogenesis imperfecta, type XII, 613849 (3), Autosomal recessive"	Sp7 (MGI:2153568)			
chr12	53380194	53416445	12q13.1	12q13.13		189906	SP1	Sp1 transcription factor	SP1	6667	ENSG00000185591			Sp1 (MGI:98372)			
chr12	53423854	53431671	12q13	12q13.13		600956	"AMHR2, AMHR"	"Anti-Mullerian hormone receptor, type II"	AMHR2	269	ENSG00000135409		"Persistent Mullerian duct syndrome, type II, 261550 (3), Autosomal recessive"	Amhr2 (MGI:105062)			
chr12	53441648	53446642	12q13.13	12q13.13		610459	"PRR13, TXR1"	Proline-rich protein 13	PRR13	54458	ENSG00000205352						
chr12	53452101	53481161	12q13.12-q13.13	12q13.13		601210	PCBP2	Poly(rC)-binding protein-2	PCBP2	5094	ENSG00000197111			Pcbp2 (MGI:108202)			
chr12	53479668	53501204	12q13	12q13.13		600447	"MAP3K12, ZPK"	Mitogen-activated protein kinase kinase kinase 12	MAP3K12	7786	ENSG00000139625			Map3k12 (MGI:1346881)			
chr12	53500920	53506430	12p12.1-q13.1	12q13.13		605053	TARBP2	TAR RNA-binding protein 2	TARBP2	6895	ENSG00000139546	pseudogene on 8q22-qter		Tarbp2 (MGI:103027)			
chr12	53507855	53626414	Chr.12	12q13.13		606371	ATF7	Activating transcription factor 7	ATF7	11016	ENSG00000170653			Atf7 (MGI:2443472)			
chr12	53665159	53677545	Chr.12	12q13.13		603193	ATP5G2	"ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C, isoform 2"	ATP5MC2	517	ENSG00000135390			Atp5g2 (MGI:1915192)			
chr12	53938791	53946543	12q13	12q13.13		142976	"HOXC13, HOX3G, ECTD9"	Homeo box-C13	HOXC13	3229	ENSG00000123364	fused with NUP98 in AML	"Ectodermal dysplasia 9, hair/nail type, 614931 (3), Autosomal recessive"	Hoxc13 (MGI:99560)			
chr12	53954867	53956605	12q13	12q13.13		142975	"HOXC12, HOX3F"	Homeo box-C12	HOXC12	3228	ENSG00000123407			Hoxc12 (MGI:96194)			
chr12	53962307	53974955	12q13.13	12q13.13		611400	HOTAIR	Hox transcript antisense RNA	HOTAIR	100124700							
chr12	53973125	53976418	Chr.12	12q13.13		605559	HOXC11	Homeo box-C11	HOXC11	3227	ENSG00000123388			Hoxc11 (MGI:96193)			
chr12	53985161	53990278	Chr.12	12q13.13		605560	HOXC10	Homeo box-C10	HOXC10	3226	ENSG00000180818			Hoxc10 (MGI:96192)			
chr12	53991737	53991846	12q13	12q13.13		609687	"MIR196A2, MIRN196A2"	Micro RNA 196A2	MIR196A2	406973							
chr12	54000118	54003336	12q13	12q13.13		142971	"HOXC9, HOX3B"	Homeo box-C9	HOXC9	3225	ENSG00000180806			Hoxc9 (MGI:96199)			
chr12	54009105	54012762	12q13	12q13.13		142970	"HOXC8, HOX3A"	Homeo box-C8	HOXC8	3224	ENSG00000037965			Hoxc8 (MGI:96198)			
chr12	54016851	54056029	12q13	12q13.13		142974	"HOXC4, HOX3E"	Homeo box-C4	HOXC4	3221	ENSG00000198353			Hoxc4 (MGI:96195)			
chr12	54016851	54035360	12q13	12q13.13		142973	"HOXC5, HOX3D"	Homeo box-C5	HOXC5	3222	ENSG00000172789			Hoxc5 (MGI:96196)			
chr12	54016851	54030822	12q13	12q13.13		142972	"HOXC6, HOX3C"	Homeo box-C6	HOXC6	3223	ENSG00000197757			Hoxc6 (MGI:96197)			
chr12	54121273	54188993	12q	12q13.13		607753	SMUG1	Single-strand-selective monofunctional uracil-DNA glycosylase 1	SMUG1	23583	ENSG00000123415			Smug1 (MGI:1918976)			
chr12	54230945	54280130	12q13.13	12q13.13		604478	"CBX5, HP1"	Chromobox homolog 5	CBX5	23468	ENSG00000094916			Cbx5 (MGI:109372)			
chr12	54280689	54287087	12q13.1	12q13.13		164017	"HNRNPA1, IBMPFD3, ALS20"	Heterogeneous nuclear ribonucleoprotein A1	HNRNPA1	3178	ENSG00000135486	mutation identified in 1 family with IBMPFD3	"Amyotrophic lateral sclerosis 20, 615426 (3), Autosomal dominant; ?Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3, 615424 (3), Autosomal dominant"				
chr12	54292106	54301036	12q13	12q13.13		601490	NFE2	"Nuclear factor, erythroid-derived 2, 45kD"	NFE2	4778	ENSG00000123405			Nfe2 (MGI:97308)			
chr12	54325089	54351850	12q13.13	12q13.13		615472	"COPZ1, COPZ"	"Coatomer protein complex, subunit zeta-1"	COPZ1	22818	ENSG00000111481			Copz1 (MGI:1929063)			
chr12	54337215	54337313	12q13.13	12q13.13		613787	"MIR148B, MIRN148B"	Micro RNA 148B	MIR148B	442892							
chr12	54362444	54365223	12q13.13	12q13.13		606383	GPR84	G protein-coupled receptor 84	GPR84	53831	ENSG00000139572			Gpr84 (MGI:1934129)			
chr12	54369128	54391609	12q13.13	12q13.13		609124	"ZNF385A, ZNF385, RZF, HZF"	Zinc finger protein 385A	ZNF385A	25946	ENSG00000161642			Zfp385a (MGI:1352495)			
chr12	54395260	54419265	12q11-q13	12q13.13		135620	"ITGA5, FNRA, VLA5A"	"Integrin, alpha-5 (fibronectin receptor, alpha subunit; very late activation protein-5, alpha subunit)"	ITGA5	3678	ENSG00000161638			Itga5 (MGI:96604)			
chr12	54455951	54473601	12q13.2	12q13.13		617484	"GTSF1, FAM112B"	Gametocyte-specific factor 1	GTSF1	121355	ENSG00000170627			Gtsf1 (MGI:1921424)			
chr12	54497710	54543114	12q13.1	12q13.1-q13.2		141180	HEM1	Hematopoietic protein-1	NCKAP1L	3071	ENSG00000123338			Nckap1l (MGI:1926063)			
chr12	54549392	54579238	12q13	12q13.2		171891	"PDE1B1, PDES1B, PDE1B"	Phosphodiesterase-1B	PDE1B	5153	ENSG00000123360			Pde1b (MGI:97523)			
chr12	54579239	54588658	12q13.2	12q13.2		613246	"PPP1R1A, IPP1, I1"	"Protein phosphatase 1, regulatory subunit 1A"	PPP1R1A	5502	ENSG00000135447			Ppp1r1a (MGI:1889595)			
chr12	54630838	54634878	12q13	12q13.2		607360	LACRT	Lacritin	LACRT	90070	ENSG00000135413						
chr12	54644590	54648492	12q13.1	12q13.2		606634	DCD	Dermcidin	DCD	117159	ENSG00000161634						
chr12	54854514	54858392	12q13.2	12q13.2		610857	SBEM	Small breast epithelial mucin	MUCL1	118430	ENSG00000172551						
chr12	54948018	54984745	12q13.2	12q13.2		615664	"TESPA1, KIAA0748"	Thymocyte-expressed positive selection-associated protein 1	TESPA1	9840	ENSG00000135426			Tespa1 (MGI:1914846)			
chr12	55019944	55030016	12q13	12q13.2		611635	"NEUROD4, MATH3"	Neurogenic differentiation 4	NEUROD4	58158	ENSG00000123307			Neurod4 (MGI:108055)			
chr12	55684567	55716036	12q13	12q13.2		600536	ITGA7	"Integrin, alpha-7"	ITGA7	3679	ENSG00000135424		"Muscular dystrophy, congenital, due to ITGA7 deficiency, 613204 (3), Autosomal recessive"	Itga7 (MGI:102700)			
chr12	55716033	55719706	12q13-q14	12q13.2		601444	GCN5L1	"GCN5 (general control of amino-acid synthesis, yeast, homolog)-like 1"	BLOC1S1	2647	ENSG00000135441			Bloc1s1 (MGI:1195276)			
chr12	55720366	55724741	12q13-q14	12q13.2		601617	RDH5	Retinol dehydrogenase-5	RDH5	5959	ENSG00000135437		"Fundus albipunctatus, 136880 (3), Autosomal recessive, Autosomal dominant"	Rdh5 (MGI:1201412)			
chr12	55725442	55729672	12q12-q13	12q13.2		155740	"CD63, MLA1"	CD63 antigen (melanoma 1 antigen)	CD63	967	ENSG00000135404			Cd63 (MGI:99529)			
chr12	55743277	55757193	12q13.13	12q13.2		603936	"GDF11, BMP11"	Growth/differentiation factor 11	GDF11	10220	ENSG00000135414			Gdf11 (MGI:1338027)			
chr12	55752462	55817755	12q13	12q13.2		610049	"SARNP, CIP29, HCC1, HSPC316"	SAP domain-containing ribonucleoprotein	SARNP	84324	ENSG00000205323	fused with MLL in AML		Sarnp (MGI:1913368)			
chr12	55818021	55821174	12q13.2	12q13.2		610074	ORMDL2	ORM1-like protein 2	ORMDL2	29095	ENSG00000123353	pseudogene on 8q22.1		Ormdl2 (MGI:1914094)			
chr12	55820959	55829635	12q13.1-q13.2	12q13.2		606092	"DRIP78, HDJ3"	"Dopamine receptor-interacting protein, 78kD"	DNAJC14	85406	ENSG00000135392			Dnajc14 (MGI:1921580)			
chr12	55835429	55842982	12q14	12q13.2		601807	"MMP19, MMP18, CODA"	Matrix metalloproteinase-19	MMP19	4327	ENSG00000123342	triplication in upstream regulatory region	"Cavitary optic disc anomalies, 611543 (3), Autosomal dominant"	Mmp19 (MGI:1927899)			
chr12	55931090	55954022	12q13.3	12q13.2		125855	"DGKA, DAGK1"	"Diacylglycerol kinase, alpha, 80kD"	DGKA	1606	ENSG00000065357			Dgka (MGI:102952)			
chr12	55954104	55966711	12q13-q14	12q13.2		155550	"SILV, D12S53E, PMEL17"	"Silver, mouse, homolog of"	PMEL	6490	ENSG00000185664			Pmel (MGI:98301)			
chr12	55966768	55972788	12q13	12q13.2		116953	CDK2	Cyclin-dependent kinase 2	CDK2	1017	ENSG00000123374			Cdk2 (MGI:104772)			
chr12	55973912	55996682	12q13	12q13.2		179514	RAB5B	Ras-associated protein RAB5B	RAB5B	5869	ENSG00000111540			Rab5b (MGI:105938)			
chr12	55992546	56005524	Chr.12	12q13.2		606887	SUOX	Sulfite oxidase	SUOX	6821	ENSG00000139531		"Sulfite oxidase deficiency, 272300 (3), Autosomal recessive"	Suox (MGI:2446117)			
chr12	56007646	56038434	12q13	12q13.2		606239	"IKZF4, ZNFN1A4, EOS, KIAA1782"	Ikaros family zinc finger 4	IKZF4	64375	ENSG00000123411			Ikzf4 (MGI:1343139)			
chr12	56041854	56044696	12q	12q13.2		603701	"RPS26, DBA10"	Ribosomal protein S26	RPS26	6231	ENSG00000197728		"Diamond-Blackfan anemia 10, 613309 (3), Autosomal dominant"	Rps26 (MGI:1351628)			
chr12	56080024	56103506	12q13	12q13.2		190151	"ERBB3, LCCS2"	Transformation gene ERBB-3	ERBB3	2065	ENSG00000065361		"Lethal congenital contractural syndrome 2, 607598 (3), Autosomal recessive"	Erbb3 (MGI:95411)			
chr12	56104318	56113909	12q13	12q13.2		602145	PA2G4	"Proliferation-associated 2G4, 38kD"	PA2G4	5036	ENSG00000170515	family of genes on 7 chromosomes		Pa2g4 (MGI:894684)			
chr12	56116589	56117831	12q13.2	12q13.2		613315	"RPL41, HG12"	Ribosomal protein L41	RPL41	6171	ENSG00000229117						
chr12	56128201	56144675	12q13.2	12q13.2		616670	"ESYT1, MBC2, FAM62A"	Extended synaptotagmin-like protein 1	ESYT1	23344	ENSG00000139641			Esyt1 (MGI:1344426)			
chr12	56152419	56157986	12q13.13	12q13.2		609930	"MYL6B, MLC1SA"	"Myosin, light chain 6B, alkali, smooth muscle and nonmuscle, slow"	MYL6B	140465	ENSG00000196465			Myl6b (MGI:1917789)			
chr12	56158260	56161581	12q13.2	12q13.2		609931	MYL6	"Myosin light chain 6, alkali, smooth muscle and nonmuscle"	MYL6	4637	ENSG00000092841			Myl6 (MGI:109318)			
chr12	56162358	56189573	12q13-q14	12q13.2		601734	"SMARCC2, BAF170"	"SW1/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2"	SMARCC2	6601	ENSG00000139613			Smarcc2 (MGI:1915344)			
chr12	56200000	57700000	12q13.3			614375	AAA4	"Aortic aneurysm, familial abdominal, 4"		100859927		associated with rs1466535	"Aortic aneurysm, familial abdominal, 4, 614375 (2)"				
chr12	56222011	56229857	12q13.3	12q13.3		612104	"OBFC2B, SSB1"	Oligonucleotide/oligosaccharide-binding fold-containing protein 2B	NABP2	79035	ENSG00000139579			Nabp2 (MGI:1917167)			
chr12	56230035	56237849	12q13.3	12q13.3		608730	"SLC39A5, MYP24"	"Solute carrier family 39 (zinc transporter), member 5"	SLC39A5	283375	ENSG00000139540		"Myopia 24, autosomal dominant, 615946 (3), Autosomal dominant"	Slc39a5 (MGI:1919336)			
chr12	56271698	56300390	12q13.2-q13.3	12q13.3		118950	CS	"Citrate synthase, mitochondrial"	CS	1431	ENSG00000062485			Cs (MGI:88529)			
chr12	56309841	56316347	12q15	12q13.3		605861	"CNPY4, TMEM4, MSAP"	"Canopy 2, zebrafish, homolog of"	CNPY2	10330	ENSG00000257727			Cnpy2 (MGI:1928477)			
chr12	56316222	56334052	12q13.3	12q13.3		617447	"PAN2, USP52, KIAA0710"	PABP-dependent poly(A) nuclease 2	PAN2	9924	ENSG00000135473			Pan2 (MGI:1918984)			
chr12	56334158	56340409	12q13.2	12q13.3		605580	"IL23A, SGRF, P19, IL23P19"	"Interleukin 23, p19 subunit"	IL23A	51561	ENSG00000110944			Il23a (MGI:1932410)			
chr12	56341596	56360252	12q13.2	12q13.3		600556	"STAT2, IMD44"	Signal transducer and activator of transcription 2	STAT2	6773	ENSG00000170581		"Immunodeficiency 44, 616636 (3), Autosomal recessive"	Stat2 (MGI:103039)			
chr12	56360570	56362798	12q13.3	12q13.3		107760	"APOF, LTIP"	Apolipoprotein F	APOF	319	ENSG00000175336			Apof (MGI:104539)			
chr12	56416372	56449464	12q12-q13	12q13.3		603887	"TIMELESS, TIM, TIM1"	"Timeless, Drosophila, homolog of"	TIMELESS	8914	ENSG00000111602			Timeless (MGI:1321393)			
chr12	56449501	56456552	12q13	12q13.3		154050	"MIP, AQP0, CTRCT15"	Major intrinsic protein of lens fiber	MIP	4284	ENSG00000135517	slightly distal to AQP2	"Cataract 15, multiple types, 615274 (3), Autosomal dominant"	Mip (MGI:96990)			
chr12	56470943	56488413	12q13	12q13.3		606365	"GLS2, GA"	"Glutaminase, liver"	GLS2	27165	ENSG00000135423			Gls2 (MGI:2143539)			
chr12	56520405	56596195	12q13.3	12q13.3		602387	"RBMS2, SCR3"	"RNA-binding motif protein, single strand interacting, 2"	RBMS2	5939	ENSG00000076067			Rbms2 (MGI:1861776)			
chr12	56595595	56636815	12q24.3-qter	12q13.3		605682	BAZ2A	"Bromodomain adjacent to zinc finger domain, 2A"	BAZ2A	11176	ENSG00000076108			Baz2a (MGI:2151152)			
chr12	56638174	56646067	12p13-qter	12q13.3		102910	"ATP5B, ATPSB"	"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide"	ATP5F1B	506	ENSG00000110955			Atp5b (MGI:107801)			
chr12	56663340	56689574	12q13.3	12q13.3		607061	"PTGES3, P23, CPGES"	Prostaglandin E synthase 3	PTGES3	10728	ENSG00000110958			"Ptges3,Ptges3-ps (MGI:1929282,MGI:3704271)"			
chr12	56712426	56726274	12q23-q24.1	12q13.3		601234	NACA	Nascent-polypeptide-associated complex alpha polypeptide	NACA	4666	ENSG00000196531			Naca (MGI:106095)			
chr12	56731579	56752361	12q13	12q13.3		176635	PRIM1	"Primase, polypeptide-1, 49kD"	PRIM1	5557	ENSG00000198056			Prim1 (MGI:97757)			
chr12	56752448	56787789	12q13	12q13.3		606623	HSE	3-alpha-hydroxysteroid epimerase	HSD17B6	8630	ENSG00000025423			Hsd17b6 (MGI:1351670)			
chr12	56923153	56934404	12q13.3	12q13.3		609769	"SDR9C7, SDRO, ARCI13"	Short chain dehydrogenase/reductase family 9C member 7	SDR9C7	121214	ENSG00000170426		"Ichthyosis, congenital, autosomal recessive 13, 617574 (3), Autosomal recessive"	Sdr9c7 (MGI:1917311)			
chr12	57009996	57016559	12q13-q21	12q13.3		162330	"TAC3, NKNB, HH10"	"Tachykinin 3 (neuromedin K, neurokinin B)"	TAC3	6866	ENSG00000166863		"Hypogonadotropic hypogonadism 10 with or without anosmia, 614839 (3), Autosomal recessive"	Tac2 (MGI:98476)			
chr12	57028516	57050764	12q13-q15	12q13.3		601478	MYO1A	Myosin IA	MYO1A	4640	ENSG00000166866			Myo1a (MGI:107732)			
chr12	57055642	57088702	12q13.3	12q13.3		616496	"NEMP1, TMEM194A"	Nuclear envelope integral membrane protein 1	NEMP1	23306	ENSG00000166881			Nemp1 (MGI:2446113)			
chr12	57088893	57095475	12q13.3-q14.1	12q13.3		602381	NAB2	NGFIA-binding protein-2	NAB2	4665	ENSG00000166886			Nab2 (MGI:107563)			
chr12	57095403	57111412	12q13	12q13.3		601512	STAT6	"Signal transducer and activator of transcription-6, interleukin-4 induced"	STAT6	6778	ENSG00000166888			Stat6 (MGI:103034)			
chr12	57128400	57213376	12q13.1-q13.3	12q13.3		107770	"LRP1, A2MR, KPA"	Low density lipoprotein-related protein-1 (alpha-2-macroglobulin receptor)	LRP1	4035	ENSG00000123384	mutation identified in 1 KPA family	"?Keratosis pilaris atrophicans, 604093 (3), Autosomal recessive"	Lrp1 (MGI:96828)			
chr12	57216794	57226448	12q13.3	12q13.3		604637	"NXPH4, NPH4"	Neuroexophilin 4	NXPH4	11247	ENSG00000182379			Nxph4 (MGI:1336197)			
chr12	57229572	57234934	12q13	12q13.3		138450	"SHMT2, GLYA"	Serine hydroxymethyltransferase	SHMT2	6472	ENSG00000182199	glycine A auxotroph		Shmt2 (MGI:1277989)			
chr12	57243452	57251192	12q13.3	12q13.3		615521	"STAC3, NAM"	SH3 and cystein-rich domains 3	STAC3	246329	ENSG00000185482		"Native American myopathy, 255995 (3), Autosomal recessive"	Stac3 (MGI:3606571)			
chr12	57434684	57452061	12q13.1	12q13.3		601233	INHBC	"Inhibin, beta C"	INHBC	3626	ENSG00000175189			Inhbc (MGI:105932)			
chr12	57455290	57458012	12q13.3	12q13.3		612031	INHBE	"Inhibin, beta E"	INHBE	83729	ENSG00000139269			Inhbe (MGI:109269)			
chr12	57460134	57472450	12q13.2-q13.3	12q13.3		165220	GLI	Glioma-associated oncogene homolog (zinc finger protein)	GLI1	2735	ENSG00000111087			Gli1 (MGI:95727)			
chr12	57472254	57488813	12q14	12q13.3		610576	ARHGAP9	Rho GTPase-activating protein 9	ARHGAP9	64333	ENSG00000123329			Arhgap9 (MGI:2143764)			
chr12	57487952	57516654	12q13.3	12q13.3		156560	"MARS, MTRNS, METRS, ILLD, CMT2U"	Methioninyl-tRNA synthetase	MARS	4141	ENSG00000166986		"Charcot-Marie-Tooth disease, axonal, type 2U, 616280 (3), Autosomal dominant; Interstitial lung and liver disease, 615486 (3), Autosomal recessive"	Mars (MGI:1345633)			
chr12	57516587	57520516	12q13.1-q13.2	12q13.3		126337	"DDIT3, GADD153, CHOP10"	DNA-damage-inducible transcript-3	DDIT3	1649	ENSG00000175197	fused with FUS in myxoid liposarcoma	"Myxoid liposarcoma, 613488 (1)"	Ddit3 (MGI:109247)			
chr12	57519162	57519258	12q13.3	12q13.3		614489	MIR616	Micro RNA 616	MIR616	693201							
chr12	57530049	57547330	12q13.3	12q13.3		607376	"DCTN2, DCTN50"	Dynactin 2	DCTN2	10540	ENSG00000175203			Dctn2 (MGI:107733)			
chr12	57549991	57586632	12q13	12q13.3		602821	"KIF5A, NKHC, SPG10, NEIMY, ALS25"	Kinesin family member 5A	KIF5A	3798	ENSG00000155980		"{Amyotrophic lateral sclerosis, susceptibility to, 25}, 617921 (3); Myoclonus, intractable, neonatal, 617235 (3), Autosomal dominant; Spastic paraplegia 10, autosomal dominant, 604187 (3), Autosomal dominant"	Kif5a (MGI:109564)			
chr12	57591158	57603427	12q13.3	12q13.3		617104	"PIP4K2C, PIP5K2C"	"Phosphatidylinositol 5-phosphate 4-kinase, type II, gamma"	PIP4K2C	79837	ENSG00000166908			Pip4k2c (MGI:2152214)			
chr12	57604326	57609803	12q13.3	12q13.3		613142	DTX3	"Deltex, Drosophila, homolog of, 3"	DTX3	196403	ENSG00000178498			Dtx3 (MGI:2135752)			
chr12	57610179	57617244	12q13.11	12q13.3		610215	"ARHGEF25, GEFT"	Rho guanine nucleotide exchange factor 25	ARHGEF25	115557	ENSG00000240771			Arhgef25 (MGI:1277173)			
chr12	57623408	57633238	12q13.3	12q13.3		601873	"B4GALNT1, GALGT, GALNACT, SPG26"	"Beta-1,4-N-acetylgalactosaminyltransferase 1"	B4GALNT1	2583	ENSG00000135454		"Spastic paraplegia 26, autosomal recessive, 609195 (3), Autosomal recessive"	B4galnt1 (MGI:1342057)			
chr12	57693954	57721556	12q13	12q13.3-q14.1		609677	OS9	Amplified in osteosarcoma 9	OS9	10956	ENSG00000135506			Os9 (MGI:1924301)			
chr12	57700000	67300000	12q14			177700	GLC1P	"Glaucoma 1, open angle, P"				caused by 300kb duplication	"Glaucoma 1, open angle, P, 177700 (4), Autosomal dominant"				
chr12	57700000	67300000	12q14			614354	PRO2268	PRO2268 gene		55390							
chr12	57723764	57742200	12q14.1	12q14.1		605476	"AGAP2, CENTG1, PIKE"	"ARF-GAP with GTP-binding protein-like, ankyrin repeat, and pleckstrin homology domains 2"	AGAP2	116986	ENSG00000135439			Agap2 (MGI:3580016)			
chr12	57744988	57748242	12q13-q14	12q14.1		181035	"TSPAN31, SAS"	Tetraspanin 31	TSPAN31	6302	ENSG00000135452			Tspan31 (MGI:1914375)			
chr12	57747726	57752446	12q14	12q14.1		123829	"CDK4, CMM3"	Cyclin-dependent kinase 4	CDK4	1019	ENSG00000135446		"{Melanoma, cutaneous malignant, 3}, 609048 (3), Autosomal dominant"	Cdk4 (MGI:88357)			
chr12	57755097	57760409	12q14.1	12q14.1		613336	9-Mar	Membrane-associated RING-CH finger protein 9	9-Mar	92979	ENSG00000139266			March9 (MGI:2446144)			
chr12	57762333	57767192	12q13.1-q13.3	12q14.1		609506	"CYP27B1, VDD1, PDDR"	"Cytochrome P450, subfamily XXVIIB, polypeptide 1"	CYP27B1	1594	ENSG00000111012		"Vitamin D-dependent rickets, type I, 264700 (3), Autosomal recessive"	Cyp27b1 (MGI:1098274)			
chr12	57768567	57772130	12q13	12q14.1		604466	METTL1	Methyltransferase-like 1	METTL1	4234	ENSG00000037897			Mettl1 (MGI:1339986)			
chr12	57772599	57782540	12q14.1	12q14.1		615258	"EEF1AKMT3, METTL21B, FAM119B"	EEF1A lysine methyltransferase 3	EEF1AKMT3	25895	ENSG00000123427			Eef1akmt3 (MGI:3645330)			
chr12	57782744	57802855	12q13-q14	12q14.1		604723	"TSFM, COXPD3"	"Ts translation elongation factor, mitochondrial"	TSFM	10102	ENSG00000123297		"Combined oxidative phosphorylation deficiency 3, 610505 (3), Autosomal recessive"	Tsfm (MGI:1913649)			
chr12	57797375	57818703	12q14	12q14.1		613397	AVIL	Advillin	AVIL	10677	ENSG00000135407			Avil (MGI:1333798)			
chr12	57824608	57824691	12q14.1	12q14.1		613057	"MIR26A2, MIRN26A2"	Micro RNA 26A2	MIR26A2	407016							
chr12	58872154	58920537	12q13.2	12q14.1		608870	"LIRG3, LIG3"	Leucine-rich repeats- and immunoglobulin-like domains-containing protein 3	LRIG3	121227	ENSG00000139263			Lrig3 (MGI:2443955)			
chr12	59595933	59789854	12q13	12q14.1		603654	"SLC16A7, MCT2"	"Solute carrier family 16 (monocarboxylic acid transporters), member 7"	SLC16A7	9194	ENSG00000118596			Slc16a7 (MGI:1330284)			
chr12	61708247	62260103	12q14.1	12q14.1		617496	"FAM19A2, TAFA2"	"Family with sequence similarity 19, member A2, CC motif chemokine-like"	FAM19A2	338811	ENSG00000198673			Fam19a2 (MGI:2143691)			
chr12	62260339	62409720	12q14.1	12q14.1		604731	USP15	Ubiquitin-specific protease 15	USP15	9958	ENSG00000135655			Usp15 (MGI:101857)			
chr12	62466816	62598955	12q14.1	12q14.1		616822	"MON2, KIAA1040"	"Mon2, S. cerevisiae, homolog of"	MON2	23041	ENSG00000061987			Mon2 (MGI:1914324)			
chr12	62603685	62603768	12q14.1	12q14.1		612148	"MIRLET7I, LET7I, MIRNLET7I"	Micro RNA Let7i	MIRLET7I	406891							
chr12	62643981	62934884	12q14.1-q14.2	12q14.1-q14.2		616016	"PPM1H, KIAA1157"	"Protein phosphatase, magnesium/manganese-dependent, 1H"	PPM1H	57460	ENSG00000111110			Ppm1h (MGI:2442087)			
chr12	62700000	64700000	12q14.2			610908	AUTS13	"Autism, susceptibility to, 13"		100188317		linkage with rs1445442	"{Autism susceptibility 13}, 610908 (2)"				
chr12	63142758	63152809	12q14-q15	12q14.2		600821	AVPR1A	Arginine vasopressin receptor-1A	AVPR1A	552	ENSG00000166148			Avpr1a (MGI:1859216)			
chr12	63558912	63669200	12q14.2	12q14.2		613893	"DPY19L2, SPGF9"	DPY19-like 2	DPY19L2	283417	ENSG00000177990	pseudogene on 7p14.3	"Spermatogenic failure 9, 613958 (3), Autosomal recessive"	Dpy19l2 (MGI:2444662)			
chr12	63779802	63809557	12q14.2	12q14.2		605862	"RXYLT1, TMEM5, MDDGA10"	Ribitol xylosyltransferase 1	RXYLT1	10329	ENSG00000118600		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 (3), Autosomal recessive"	Tmem5 (MGI:2384919)			
chr12	63843910	64147862	12q14.2	12q14.2		606523	"SRGAP1, KIAA1304, NMTC2"	"Slit-robo GTPase-activating protein, rho, 1"	SRGAP1	57522	ENSG00000196935		"{Thyroid cancer, nonmedullary, 2}, 188470 (3), Autosomal dominant"	Srgap1 (MGI:2152936)			
chr12	64186311	64222295	12q14.2	12q14.2		617420	C12orf66	Chromosome 12 open reading frame 66	C12orf66	144577	ENSG00000174206			BC048403 (MGI:2670984)			
chr12	64452059	64502118	12q14.2	12q14.2		604834	"TBK1, NAK, FTDALS4, IIAE8"	TANK-binding kinase 1	TBK1	29110	ENSG00000183735		"{Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8}, 617900 (3), Autosomal dominant; Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 (3), Autosomal dominant"	Tbk1 (MGI:1929658)			
chr12	64610512	64697566	12q14.1	12q14.2		607019	RASSF3	Ras association domain family protein 3	RASSF3	283349	ENSG00000153179			Rassf3 (MGI:2179722)			
chr12	64700000	67300000	12q14.3			611547	STQTL9	Stature quantitative trait locus 9				associated with rs1042725	"{Stature QTL 9}, 611547 (2)"				
chr12	64713441	64759445	12q14	12q14.3		607664	"GNS, G6S"	N-acetylglucosamine-6-sulfatase	GNS	2799	ENSG00000135677		"Mucopolysaccharidosis type IIID, 252940 (3), Autosomal recessive"	Gns (MGI:1922862)			
chr12	64759496	64881021	12q14.3	12q14.3		615077	"TBC1D30, KIAA0984"	"TBC1 domain family, member 30"	TBC1D30	23329	ENSG00000111490			Tbc1d30 (MGI:1921944)			
chr12	65050623	65121565	Chr.12	12q14.3		605186	WIF1	WNT inhibitory factor 1	WIF1	11197	ENSG00000156076			Wif1 (MGI:1344332)			
chr12	65169570	65248360	12q14	12q14.3		607844	"LEMD3, MAN1"	LEM domain-containing 3	LEMD3	23592	ENSG00000174106		"Buschke-Ollendorff syndrome, 166700 (3), Autosomal dominant; Osteopoikilosis with or without melorheostosis, 166700 (3), Autosomal dominant"	Lemd3 (MGI:3580376)			
chr12	65278592	65466906	12q14.3	12q14.3		613719	"MSRB3, DFNB74"	Methionine sulfoxide reductase B3	MSRB3	253827	ENSG00000174099		"Deafness, autosomal recessive 74, 613718 (3), Autosomal recessive"	Msrb3 (MGI:2443538)			
chr12	65824459	65966290	12q14.3	12q14.3		600698	"HMGA2, HMGIC, BABL"	High-mobility group AT-hook 2	HMGA2	8091	ENSG00000149948	"fusion partners with RAD51B, ALDH2, COX6C, HEI10 in uterine leiomyomas"	"Leiomyoma, uterine, somatic, 150699 (1)"				
chr12	66123068	66130752	12q14.3	12q14.3		616998	LLPH	"LLP, Aplysia, homolog of"	LLPH	84298	ENSG00000139233			"Llph-ps1,Llph-ps2,Llph (MGI:3649506,MGI:1913475,MGI:3642864)"			
chr12	66136935	66170071	12q14.3	12q14.3		616874	"TMBIM4, GAAP"	Transmembrane BAX inhibitor motif-containing protein 4	TMBIM4	51643	ENSG00000155957			Tmbim4 (MGI:1915462)			
chr12	66189197	66254621	12q14.3	12q14.3		604459	"IRAK3, IRAKM, ASRT5"	Interleukin 1 receptor-associated kinase 3	IRAK3	11213	ENSG00000090376		"{Asthma susceptibility 5}, 611064 (3)"	Irak3 (MGI:1921164)			
chr12	66302544	66343642	12q13	12q14.3		614539	"HELB, HDHB"	"Helicase, DNA, B"	HELB	92797	ENSG00000127311			Helb (MGI:2152895)			
chr12	66347430	67069264	12q14.3	12q14.3		604597	"GRIP1, FRASRS3"	Glutamate receptor-interacting protein 1	GRIP1	23426	ENSG00000155974		"Fraser syndrome 3, 617667 (3), Autosomal recessive"	Grip1 (MGI:1921303)			
chr12	67269280	67314691	12q14.3-q15	12q14-q15		607727	"CAND1, TIP120A, TIP120, KIAA0829"	Cullin-associated neddylation-dissociated protein 1	CAND1	55832	ENSG00000111530			Cand1 (MGI:1261820)			
chr12	67300000	71100000	12q15			612639	IBD26	Inflammatory bowel disease 26		100271838		associated with rs1558744	"{Inflammatory bowel disease 26}, 612639 (2)"				
chr12	67648731	67665404	12q14	12q15		603496	DYRK2	Dual-specificity tyrosine phosphorylation-regulated kinase 2	DYRK2	8445	ENSG00000127334			Dyrk2 (MGI:1330301)			
chr12	68154769	68159740	12q14	12q15		147570	"IFNG, IFG, IFI"	"Interferon, gamma"	IFNG	3458	ENSG00000111537	"3 introns; none in IFF, IFL"	"{AIDS, rapid progression to}, 609423 (3); {Aplastic anemia}, 609135 (3); {Hepatitis C virus, response to therapy of}, 609532 (3); {TSC2 angiomyolipomas, renal, modifier of}, 613254 (3), Autosomal dominant; {Tuberculosis, protection against}, 607948 (3)"	Ifng (MGI:107656)			
chr12	68201348	68225790	12q15	12q15		605679	"IL26, AK155"	Interleukin 26	IL26	55801	ENSG00000111536						
chr12	68248244	68253500	12q15	12q15		605330	"IL22, IL21, ILTIF"	Interleukin 22	IL22	50616	ENSG00000127318			"Il22,Iltifb (MGI:1355307,MGI:2151139)"			
chr12	68294565	68332413	12q15	12q15		613813	MDM1	Mouse double minute 1 homolog	MDM1	56890	ENSG00000111554			Mdm1 (MGI:96951)			
chr12	68610838	68660604	12q14	12q15		179530	RAP1B	RAS-related protein RAP1B	RAP1B	5908	ENSG00000127314			Rap1b (MGI:894315)			
chr12	68686950	68745813	12q15	12q15		607617	"NUP107, NUP84, NPHS11"	"Nucleoporin, 107kD"	NUP107	57122	ENSG00000111581		"Nephrotic syndrome, type 11, 616730 (3), Autosomal recessive"	Nup107 (MGI:2143854)			
chr12	68808148	68845543	12q14.3-q15	12q15		164785	"MDM2, ACTFS"	"Mouse double minute 2, homolog of (p53-binding protein)"	MDM2	4193	ENSG00000135679		"{Accelerated tumor formation, susceptibility to}, 614401 (3)"	Mdm2 (MGI:96952)			
chr12	68842192	68963239	12q15	12q15		114860	CPM	Carboxypeptidase M	CPM	1368	ENSG00000135678			Cpm (MGI:1917824)			
chr12	69239536	69274357	Chr.12	12q15		604979	"CPSF6, CFIM"	"Cleavage and polyadenylation specific factor 6, 68kD subunit"	CPSF6	11052	ENSG00000111605			Cpsf6 (MGI:1913948)			
chr12	69348353	69354232	12q15	12q15		153450	LYZ	Lysozyme	LYZ	4069	ENSG00000090382		"Amyloidosis, renal, 105200 (3), Autosomal dominant"	"Lyz1,Lyz2 (MGI:96902,MGI:96897)"			
chr12	69359704	69427076	12q13-q15	12q15		602116	"YEATS4, GAS41"	YEATS domain-containing protein 4	YEATS4	8089	ENSG00000127337			Yeats4 (MGI:1927224)			
chr12	69470348	69579792	12q15	12q15		607743	"FRS2, FRS1A, SNT1"	Fibroblast growth factor receptor substrate 2	FRS2	10818	ENSG00000166225			Frs2 (MGI:1100860)			
chr12	69585427	69601576	Chr.12	12q15		605139	"CCT2, CCTB"	"Chaperonin containing T-complex polypeptide 1, subunit 2"	CCT2	10576	ENSG00000166226			Cct2 (MGI:107186)			
chr12	69608563	69611161	12q15	12q15		610846	"LRRC10, HRLRRP"	Leucine-rich repeat-containing protein 10	LRRC10	376132	ENSG00000198812			Lrrc10 (MGI:2448063)			
chr12	69643507	69738363	12q14.2-q15	12q15		607337	"BEST3, VMD2L3"	Bestrophin 3	BEST3	144453	ENSG00000127325			Best3 (MGI:3580298)			
chr12	70242992	70354992	12q15	12q15		604909	"CNOT2, NOT2"	"CCR4-NOT transcription complex, subunit 2"	CNOT2	4848	ENSG00000111596			Cnot2 (MGI:1919318)			
chr12	70366219	70434291	12q14.1-q15	12q15		605223	KCNMB4	"Potassium large conductance calcium-activated channel, subfamily M, beta member 4"	KCNMB4	27345	ENSG00000135643			Kcnmb4 (MGI:1913272)			
chr12	70515870	70637439	12q15-q21	12q15		176882	PTPRB	"Protein tyrosine phosphatase, receptor type, beta polypeptide"	PTPRB	5787	ENSG00000127329			Ptprb (MGI:97809)			
chr12	70638072	70920803	12q15	12q15		602853	"PTPRR, PCPTP1"	"Protein-tyrosine phosphatase, receptor type, R"	PTPRR	5801	ENSG00000153233			Ptprr (MGI:109559)			
chr12	71100000	108600000	12q21-q23			612715	DUH2	Dyschromatosis universalis hereditaria 2		100301525		between rs1921045 and rs2373584	"Dyschromatosis universalis hereditaria 2, 612715 (2)"				
chr12	71100000	108600000	12q21-q23			603221	MYP3	"Myopia, high grade, 3, autosomal dominant"	MYP3	8782			"Myopia-3, 603221 (2), Autosomal dominant"				
chr12	71100000	92200000	12q21			169900	PEPB	Peptidase B	PEPB	5182							
chr12	71125092	71157998	12q14.1-q21.1	12q21.1		600769	"TSPAN8, TM4SF3"	Tetraspanin 8	TSPAN8	7103	ENSG00000127324			Tspan8 (MGI:2384918)			
chr12	71439769	71586309	12q15-q23	12q21.1		606667	"GPR49, LGR5"	G protein-coupled receptor-49	LGR5	8549	ENSG00000139292			Lgr5 (MGI:1341817)			
chr12	71663896	71680647	12q21.1	12q21.1		612531	THAP2	THAP domain-containing protein 2	THAP2	83591	ENSG00000173451			Thap2 (MGI:1914066)			
chr12	71754862	71793475	12q21.1	12q21.1		612398	"RAB21, KIAA0118"	RAB-associated protein RAB21	RAB21	23011	ENSG00000080371			Rab21 (MGI:894308)			
chr12	71839706	71926848	12q21.1	12q21.1		612662	TBC1D15	"TBC1 domain family, member 15"	TBC1D15	64786	ENSG00000121749			Tbc1d15 (MGI:1913937)			
chr12	71938845	72032440	12q21.1	12q21.1		607478	"TPH2, NTPH, ADHD7"	Tryptophan hydroxylase 2	TPH2	121278	ENSG00000139287		"{Attention deficit-hyperactivity disorder, susceptibility to, 7}, 613003 (3); {Unipolar depression, susceptibility to}, 608516 (3)"	Tph2 (MGI:2651811)			
chr12	72087287	72666661	12q15-q21	12q21.1		606950	TRHDE	Thyrotropin-releasing hormone-degrading ectoenzyme	TRHDE	29953	ENSG00000072657			Trhde (MGI:2384311)			
chr12	74537770	74541451	12q21	12q21.1		615579	ATXN7L3B	Ataxin 7-like 3B	ATXN7L3B	552889	ENSG00000253719			Atxn7l3b (MGI:1914971)			
chr12	75040077	75209747	12q21.1	12q21.1		176256	KCNC2	"Potassium voltage-gated channel, Shaw-related subfamily, member 2"	KCNC2	3747	ENSG00000166006	previously on 19q13.3-q13.4		Kcnc2 (MGI:96668)			
chr12	75275978	75390936	12q15	12q21.1-q21.2		607724	CAPS2	Calcyphosine 2	CAPS2	84698	ENSG00000180881			Caps2 (MGI:2441980)			
chr12	75331833	75370389	12q21	12q21.2		610395	GLIPR1L1	GLIPR1-like protein 1	GLIPR1L1	256710	ENSG00000173401			"Glipr1l1,Glipr1l3 (MGI:1916536,MGI:3620621)"			
chr12	75391069	75432687	12q21	12q21.2		610394	GLIPR1L2	GLIPR1-like protein 2	GLIPR1L2	144321	ENSG00000180481			Glipr1l2 (MGI:1914787)			
chr12	75480732	75501935	12q21	12q21.2		602692	"GLIPR1, GLIPR, RTVP1"	Glioma pathogenesis-related protein 1	GLIPR1	11010	ENSG00000139278			Glipr1 (MGI:1920940)			
chr12	75497638	75511637	12q21.2	12q21.2		612817	KRR1	"KRR1, yeast, homolog of"	KRR1	11103	ENSG00000111615			Krr1 (MGI:1289274)			
chr12	76025446	76031775	12q15-q21.2	12q21.2		605335	"PHLDA1, TDAG51"	"Pleckstrin homology-like domain, family A, member 1"	PHLDA1	22822	ENSG00000139289			Phlda1 (MGI:1096880)			
chr12	76044744	76085032	12q21.2	12q21.2		164060	"NAP1L1, NAP1L"	Nucleosome assembly protein 1-like 1	NAP1L1	4673	ENSG00000187109			Nap1l1 (MGI:1855693)			
chr12	76344485	76348441	12q21.2	12q21.2		610148	"BBS10, C12orf58, FLJ23560"	BBS10 gene	BBS10	79738	ENSG00000179941		"Bardet-Biedl syndrome 10, 615987 (3), Autosomal recessive"	Bbs10 (MGI:1919019)			
chr12	76351796	76559808	12p	12q21.2		606736	"OSBPL8, ORP8, KIAA1451"	Oxysterol-binding protein-like protein 8	OSBPL8	114882	ENSG00000091039			Osbpl8 (MGI:2443807)			
chr12	76764073	76853700	12q14-q15	12q21.2		607799	"ZDHHC17, HIP14"	Zinc finger DHHC domain-containing protein 17	ZDHHC17	23390	ENSG00000186908			Zdhhc17 (MGI:2445110)			
chr12	76858714	76879039	12q21.1	12q21.2		601871	"CSRP2, LMO5"	"Cysteine and glycine-rich protein-2 (LIM domain only 5, smooth muscle)"	CSRP2	1466	ENSG00000175183	pseudogene on 3q21.1		Csrp2 (MGI:1202907)			
chr12	77021245	77065579	12q21.3	12q21.2		612046	E2F7	E2F transcription factor 7	E2F7	144455	ENSG00000165891			E2f7 (MGI:1289147)			
chr12	77571855	78213011	12q21.1	12q21.2		611629	"NAV3, POMFIl1, KIAA0938"	Neuron navigator 3	NAV3	89795	ENSG00000067798			Nav3 (MGI:2183703)			
chr12	78863992	79452007	12cen-q21	12q21.2		185605	SYT1	Synaptotagmin-1	SYT1	6857	ENSG00000067715			Syt1 (MGI:99667)			
chr12	79584873	79691096	12q21	12q21.2		601936	"PAWR, PAR4"	"PRKC, apoptosis, WT1, regulator"	PAWR	5074	ENSG00000177425			Pawr (MGI:2149961)			
chr12	79773562	79935763	12q15-q21.2	12q21.2-q21.3		602021	"PPP1R12A, MYPT1"	"Protein phosphatase 1, regulatory subunit 12A (myosin phosphatase target subunit 1)"	PPP1R12A	4659	ENSG00000058272			Ppp1r12a (MGI:1309528)			
chr12	80130376	80379089	12q21.31	12q21.31		614925	"OTOGL, C12orf64, DFNB84B"	Otogelin-like protein	OTOGL	283310	ENSG00000165899		"Deafness, autosomal recessive 84B, 614944 (3), Autosomal recessive"	Otogl (MGI:3647600)			
chr12	80424260	80680272	12q21.2	12q21.31		603317	"PTPRQ, PTPGMC1, DFNB84A, DFNA73"	"Protein-tyrosine phosphatase, receptor-type, Q"	PTPRQ	374462	ENSG00000139304	mutation identified in 1 DFNA73 family	"Deafness, autosomal dominant 73, 617663 (3), Autosomal dominant; Deafness, autosomal recessive 84A, 613391 (3), Autosomal recessive"	Ptprq (MGI:1096349)			
chr12	80707628	80709477	12q21	12q21.31		159991	"MYF6, CNM3"	Myogenic factor-6	MYF6	4618	ENSG00000111046	"6.5kb upstream from MYF5; both prob. 12q15, by H"	"Centronuclear myopathy 3, 614408 (3), Autosomal dominant"	Myf6 (MGI:97253)			
chr12	80716928	80719667	12q21	12q21.31		159990	MYF5	Myogenic factor-5	MYF5	4617	ENSG00000111049			Myf5 (MGI:97252)			
chr12	80792519	80937914	12q21.31	12q21.31		603380	"LIN7A, VELI1, MALS1"	"Lin7, C. elegans, homolog of, A"	LIN7A	8825	ENSG00000111052			Lin7a (MGI:2135609)			
chr12	81078017	81256758	12q21.31	12q21.31		614356	ACSS3	"Acyl-CoA synthetase short-chain family, member 3"	ACSS3	79611	ENSG00000111058			Acss3 (MGI:2685720)			
chr12	82686951	83134867	12q21.31	12q21.31		615856	TMTC2	Transmembrane and tetratricopeptide repeat domains-containing protein 2	TMTC2	160335	ENSG00000179104			Tmtc2 (MGI:1914057)			
chr12	84859487	84912828	12q21.3-q21.4	12q21.31		607971	"SLC6A15, SBAT1"	"Solute carrier family 6 (neurotransmitter transporter), member 15"	SLC6A15	55117	ENSG00000072041			Slc6a15 (MGI:2143484)			
chr12	85280257	85301783	12q21.3-q22	12q21.31		601527	"ALX1, CART1, FND3"	Aristaless-like homeobox 1 (cartilage homeoprotein 1)	ALX1	8092	ENSG00000180318	mutation identified in 1 FND3 patient	"?Frontonasal dysplasia 3, 613456 (3)"	Alx1 (MGI:104621)			
chr12	85800702	85836539	12q21.31	12q21.31		610383	"RASSF9, PAMCI, PCIP1"	"Ras association domain family, member 9"	RASSF9	9182	ENSG00000198774			Rassf9 (MGI:2384307)			
chr12	85874294	85882991	12q21	12q21.31		162650	NTS	Neurotensin	NTS	4922	ENSG00000133636			Nts (MGI:1328351)			
chr12	85972280	86839005	12q21	12q21.31-q21.32		607385	GNTIVH	"UDP-N-acetylglucosamine:alpha-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IV"	MGAT4C	25834	ENSG00000182050			Mgat4c (MGI:1914819)			
chr12	88049012	88142215	12q21.3	12q21.32		610142	"CEP290, KIAA0373, 3H11AG, JBTS5, SLSN6, LCA10, BBS14"	"Centrosomal protein, 290kD"	CEP290	80184	ENSG00000198707	mutation identified in 1 BBS14 family	"?Bardet-Biedl syndrome 14, 615991 (3), Autosomal recessive; Joubert syndrome 5, 610188 (3), Autosomal recessive; Leber congenital amaurosis 10, 611755 (3); Meckel syndrome 4, 611134 (3), Autosomal recessive; Senior-Loken syndrome 6, 610189 (3), Autosomal recessive"	Cep290 (MGI:2384917)			
chr12	88142295	88199886	12q21.32	12q21.32		617218	"TMTC3, SMILE, LIS8"	Transmembrane and tetratricopeptide repeat domains-containing protein 3	TMTC3	160418	ENSG00000139324		"Lissencephaly 8, 617255 (3), Autosomal recessive"	Tmtc3 (MGI:3036255)			
chr12	88492792	88580472	12q22	12q21.32		184745	"KITLG, MGF, SF, SCF, SHEP7, FPHH, DCUA, DFNA69"	"KIT ligand (mast cell growth factor; steel, mouse, homolog of)"	KITLG	4254	ENSG00000049130	associated with dbSNP rs12821256	"Deafness, autosomal dominant 69, unilateral or asymmetric, 616697 (3), Autosomal dominant; Hyperpigmentation with or without hypopigmentation, 145250 (3), Autosomal dominant; [Skin/hair/eye pigmentation 7, blond/brown hair], 611664 (3)"	Kitl (MGI:96974)			
chr12	88600000	92200000	12q21.33			121400	CNA1	"Cornea plana 1, autosomal dominant"	CNA1	1255		between D12S82 and D12S351	"Cornea plana 1, autosomal dominant, 121400 (2), Autosomal dominant"				
chr12	88600000	92200000	12q21.33			612868	PACD	"Corneal dystrophy, posterior amorphous"				contiguous gene deletion syndrome	"Corneal dystrophy, posterior amorphous, 612868 (4), Autosomal dominant"				
chr12	89347824	89352858	12q21.33	12q21.33		602748	"DUSP6, MKP3, PYST1, HH19"	Dual-specificity phosphatase-6	DUSP6	1848	ENSG00000139318		"Hypogonadotropic hypogonadism 19 with or without anosmia, 615269 (3), Autosomal dominant"	Dusp6 (MGI:1914853)			
chr12	89419717	89526261	12q21.33	12q21.33		614784	"POC1B, PIX1, CORD20"	"POC1 centriolar protein, Chlamydomonas, homolog of, B"	POC1B	282809	ENSG00000139323		"Cone-rod dystrophy 20, 615973 (3), Autosomal recessive"	Poc1b (MGI:1918511)			
chr12	89519411	89524805	12q21.3-q22	12q21.33		603565	"GALNT4, GalNAcT4"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 4	GALNT4	8693	ENSG00000257594			Galnt4 (MGI:894692)			
chr12	89588048	89709352	12q21-q23	12q21.33		108731	"ATP2B1, PMCA1"	"ATPase, Ca++ transporting, plasma membrane, 1"	ATP2B1	490	ENSG00000070961			Atp2b1 (MGI:104653)			
chr12	90963678	91005025	12q21	12q21.33		601657	"EPYC, DSPG3"	Epiphycan	EPYC	1833	ENSG00000083782			Epyc (MGI:107942)			
chr12	91050490	91058353	12q22	12q21.33		603288	"KERA, CNA2"	Keratocan	KERA	11081	ENSG00000139330		"Cornea plana 2, autosomal recessive, 217300 (3), Autosomal recessive"	Kera (MGI:1202398)			
chr12	91103454	91111764	12q21.3-q22	12q21.33		600616	"LUM, LDC"	Lumican	LUM	4060	ENSG00000139329			Lum (MGI:109347)			
chr12	91143276	91183123	12q21.3	12q21.33		125255	"DCN, CSCD"	Decorin	DCN	1634	ENSG00000011465	conflicting assignments to 12q23 and 12q13.2	"Corneal dystrophy, congenital stromal, 610048 (3), Autosomal dominant"	Dcn (MGI:94872)			
chr12	92140277	92145896	12q22	12q21.33		109580	BTG1	"B-cell translocation gene 1, anti-proliferative"	BTG1	694	ENSG00000133639			Btg1 (MGI:88215)			
chr12	92200000	108600000	12q22-q23.3			608096	"ETL2, FTLE"	"Epilepsy, familial temporal lobe"		619399		max lod at D12S1706	"Epilepsy, familial temporal lobe, 2, 608096 (2), Autosomal dominant"				
chr12	92200000	103500000	12q22-q23.2			608520	MDD1	Major depressive disorder		431708		max lod with D12S1706	"Major depressive disorder 1, 608516 (2)"				
chr12	92420085	92432998	12q22	12q22		616989	CLLU1OS	"Chronic lymphocytic leukemia upregulated 1, opposite strand"	CLLU1OS	574016	ENSG00000205057						
chr12	92421530	92431001	12q22	12q22		616988	CLLU1	Chronic lymphocytic leukemia upregulated gene 1	CLLU1	574028							
chr12	92772508	92975227	12q22	12q22		605070	EEA1	Early endosome antigen 1	EEA1	8411				Eea1 (MGI:2442192)			
chr12	93408311	93442335	12q22	12q22		603679	"UBE2N, UBCHBEN; UBC13"	Ubiquitin-conjugating enzyme E2N	UBE2N	7334	ENSG00000177889			Ube2n (MGI:1934835)			
chr12	93467489	93503771	12q22	12q22		611847	"MRPL42, MRPL31, MRPS32"	Mitochondrial ribosomal protein L42	MRPL42	28977	ENSG00000198015			Mrpl42 (MGI:1333774)			
chr12	93565627	93571397	12q22	12q22		617269	SOCS2AS1	SOCS2 antisense RNA 1	SOCS2-AS1	144481							
chr12	93677341	93894839	12q21.33-q23.1	12q22		603454	"CRADD, RAIDD, MRT34"	Caspase and RIP adaptor with death domain	CRADD	8738	ENSG00000169372		"Mental retardation, autosomal recessive 34, with variant lissencephaly, 614499 (3), Autosomal recessive"	Cradd (MGI:1336168)			
chr12	94265651	94460615	12q22	12q22		615847	"CEP83, CCDC41, NPHP18"	"Centrosomal protein, 83kD"	CEP83	51134	ENSG00000173588		"Nephronophthisis 18, 615862 (3), Autosomal recessive"	Cep83 (MGI:1924298)			
chr12	94148722	94307674	Chr.12	12q22		604259	VESPR	Virus-encoded semaphorin protein receptor	PLXNC1	10154	ENSG00000136040			Plxnc1 (MGI:1890127)			
chr12	94567123	94650561	12q22	12q22		617459	TMCC3	"Transmembrane and coiled-coil domain family, member 3"	TMCC3	57458	ENSG00000057704			Tmcc3 (MGI:2442900)			
chr12	94834397	94834512	12q22	12q22		614384	MIR492	Micro RNA 492	MIR492	574449		within KRT19					
chr12	94971327	95003712	12q22	12q22		614530	NDUFA12	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 12"	NDUFA12	55967	ENSG00000184752		"Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufa12 (MGI:1913664)			
chr12	95020228	95073627	12q22	12q22		601529	"NR2C1, TR2"	"Nuclear receptor subfamily 2, group C, member 1"	NR2C1	7181	ENSG00000120798			Nr2c1 (MGI:1352465)			
chr12	95076748	95217463	12q22	12q22		613520	"FGD6, ZFYVE24"	"FYVE, RhoGEF, and ph domain-containing protein 6"	FGD6	55785	ENSG00000180263			Fgd6 (MGI:1261419)			
chr12	95474045	95515838	12q22	12q22		601870	"METAP2, p67"	Methionine aminopeptidase 2	METAP2	10988	ENSG00000111142			Metap2 (MGI:1929701)			
chr12	95516559	95551528	12q22	12q22		610993	USP44	Ubiquitin-specific protease 44	USP44	84101	ENSG00000136014			Usp44 (MGI:3045318)			
chr12	95657806	95791205	12q22-q23	12q22		610401	NTN4	Netrin 4	NTN4	59277	ENSG00000074527			Ntn4 (MGI:1888978)			
chr12	95800000	133275309	12q23-q24			613096	SPG36	Spastic paraplegia-36	SPG36	791228		between D12S360 and D12S354	"Spastic paraplegia 36, autosomal dominant, 613096 (2), Autosomal dominant"				
chr12	95858930	95866459	12q23.1	12q23.1		603541	SNRPF	Small nuclear ribonucleoprotein polypeptide F	SNRPF	6636	ENSG00000139343			Snrpf (MGI:1917128)			
chr12	95972661	95996364	12q22-q23	12q23.1		609457	"HAL, HSTD"	Histidine ammonia-lyase (histidase)	HAL	3034	ENSG00000084110		"[Histidinemia], 235800 (3), Autosomal recessive, Autosomal dominant"	Hal (MGI:96010)			
chr12	96000752	96043519	12q22	12q23.1		151570	LTA4H	Leukotriene A4 hydrolase	LTA4H	4048	ENSG00000111144			Lta4h (MGI:96836)			
chr12	96194381	96269834	12q23	12q23.1		600247	"ELK3, SAP2, ERP"	"ELK3, ETS-domain protein (SRF accessory protein 2)"	ELK3	2004	ENSG00000111145			Elk3 (MGI:101762)			
chr12	96278260	96400587	12q23.1	12q23.1		603440	"CDK17, PCTK2, PCTAIRE2"	Cyclin-dependent kinase 17	CDK17	5128	ENSG00000059758			Cdk17 (MGI:97517)			
chr12	96907221	96953690	12q22	12q23.1		600372	NEDD1	"Neural precursor cell expressed, developmentally down-regulated 1"	NEDD1	121441	ENSG00000139350			Nedd1 (MGI:97293)			
chr12	97462775	97565014	12q21	12q23.1		607045	"RMST, NCRMS, NCRNA00054"	Rhabdomyosarcoma 2-associated transcript	RMST	196475							
chr12	98515572	98550378	12q22	12q23.1		188380	"TMPO, LAP2"	Thymopoietin	TMPO	7112	ENSG00000120802			Tmpo (MGI:106920)			
chr12	98593624	98601999	12q23	12q23.1		600370	"SLC25A3, PHC"	"Solute carrier family 25 (mitochondrial carrier), member 3"	SLC25A3	5250	ENSG00000075415		"Mitochondrial phosphate carrier deficiency, 610773 (3)"	Slc25a3 (MGI:1353498)			
chr12	98613403	98645050	12q23	12q23.1		609861	IKIP	I-kappa-B kinase-interacting protein	IKBIP	121457	ENSG00000166130			Ikbip (MGI:1914704)			
chr12	98645140	98735432	12q23	12q23.1		602233	APAF1	Apoptotic protease activating factor 1	APAF1	317	ENSG00000120868			Apaf1 (MGI:1306796)			
chr12	98729903	99984772	12q23.1	12q23.1		607815	"ANKS1B, EB1"	Ankyrin repeat and sterile alpha motif domain-containing protein 1B	ANKS1B	56899	ENSG00000185046			Anks1b (MGI:1924781)			
chr12	100267139	100341723	12q23.1	12q23.1		616365	"SCYL2, CVAK104, KIAA1360"	SCY1-like protein 2	SCYL2	55681	ENSG00000136021			Scyl2 (MGI:1289172)			
chr12	100357078	100422058	12q23	12q23.1		607557	"SLC17A8, VGLUT3, DFNA25"	"Solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 (vesicular glutamate transporter 3)"	SLC17A8	246213	ENSG00000179520		"Deafness, autosomal dominant 25, 605583 (3), Autosomal dominant"	Slc17a8 (MGI:3039629)			
chr12	100473772	100563866	12q23.1	12q23.1		603826	"NR1H4, FXR, RIP14, PFIC5"	Nuclear receptor subfamily 1 group H member 4	NR1H4	9971	ENSG00000012504		"Cholestasis, progressive familial intrahepatic, 5, 617049 (3), Autosomal recessive"	Nr1h4 (MGI:1352464)			
chr12	100573660	100628287	12q23.1	12q23.1		617224	"GAS2L3, G2L3"	Growth arrest-specific 2-like 3	GAS2L3	283431	ENSG00000139354			Gas2l3 (MGI:1918780)			
chr12	100717456	101128640	12q23	12q23.1		610111	"TMEM16D, FLJ34272"	Transmembrane protein 16D	ANO4	121601	ENSG00000151572			Ano4 (MGI:2443344)			
chr12	101156215	101210273	12q22-q23	12q23.1-q23.2		608044	"SLC5A8, AIT, SMCT"	"Solute carrier family (iodide transporter), member 8"	SLC5A8	160728	ENSG00000256870			Slc5a8 (MGI:2384916)			
chr12	101200000	103500000	12q23.2			614985	"HELLPAR, lncHELLP"	HELLP syndrome-associated long noncoding RNA	HELLPAR	101101692							
chr12	101280126	101386618	12q23.2-q23.3	12q23.2		612822	"UTP20, DRIM"	"UTP20, S. cerevisiae, homolog of"	UTP20	27340	ENSG00000120800			Utp20 (MGI:1917933)			
chr12	101393119	101407819	12q23.2	12q23.2		603425	ARL1	ADP-ribosylation factor-like 1	ARL1	400	ENSG00000120805			Arl1 (MGI:99436)			
chr12	101475275	101486996	12q22	12q23.2		612568	SPIC	SPIC transcription factor	SPIC	121599	ENSG00000166211			Spic (MGI:1341168)			
chr12	101594848	101695840	12q23.2	12q23.2		160794	"MYBPC1, LCCS4"	"Myosin-binding protein C, slow type"	MYBPC1	4604	ENSG00000196091		"Arthrogryposis, distal, type 1B, 614335 (3), Autosomal dominant; Lethal congenital contracture syndrome 4, 614915 (3), Autosomal recessive"	Mybpc1 (MGI:1336213)			
chr12	101697638	101752037	12q23.2	12q23.2		616747	"CHPT1, CPT, CPT1"	Choline phosphotransferase 1	CHPT1	56994	ENSG00000111666			Chpt1 (MGI:2384841)			
chr12	101728647	101739720	12q23	12q23.2		604759	"SYCP3, SCP3, COR1, SPGF4, RPRGL4"	Synaptonemal complex protein 3	SYCP3	50511	ENSG00000139351		"Pregnancy loss, recurrent, 4, 270960 (3), Autosomal dominant; Spermatogenic failure 4, 270960 (3), Autosomal dominant"	Sycp3 (MGI:109542)			
chr12	101745496	101830866	12q23.3	12q23.2		607840	"GNPTAB, GNPTA"	"N-acetylglucosamine-1-phosphate transferase, alpha/beta subunits"	GNPTAB	79158	ENSG00000111670	conflicting assignment to 4q	"Mucolipidosis II alpha/beta, 252500 (3), Autosomal recessive; Mucolipidosis III alpha/beta, 252600 (3), Autosomal recessive"	Gnptab (MGI:3643902)			
chr12	101877326	101923622	12q23.2	12q23.2		610776	DRAM1	Damage-regulated autophagy modulator 1	DRAM1	55332	ENSG00000136048			Dram1 (MGI:1918962)			
chr12	102073961	102120130	12q23.2	12q23.2		609264	"NUP37, p37"	"Nucleoporin, 37kD"	NUP37	79023	ENSG00000075188			Nup37 (MGI:1919964)			
chr12	102120170	102197519	12q23	12q23.2		613687	"C12orf48, AROM, PARPBP"	Chromosome 12 open reading frame 48	PARPBP	55010	ENSG00000185480			Parpbp (MGI:1922567)			
chr12	102196458	102199539	12q23-q24	12q23.2		176795	PMCH	Pro-melanin-concentrating hormone	PMCH	5367	ENSG00000183395			Pmch (MGI:97629)			
chr12	102395859	102481838	12q22-q24.1	12q23.2		147440	IGF1	"Insulin-like growth factor-1, or somatomedin C"	IGF1	3479	ENSG00000017427		"Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747 (3), Autosomal recessive"	Igf1 (MGI:96432)			
chr12	102836884	102958409	12q24.1	12q23.2		612349	"PAH, PKU1"	Phenylalanine hydroxylase	PAH	5053	ENSG00000171759	close to IGF1	"[Hyperphenylalaninemia, non-PKU mild], 261600 (3), Autosomal recessive; Phenylketonuria, 261600 (3), Autosomal recessive"	Pah (MGI:97473)			
chr12	102957673	102960515	12q22-q23	12q23.2		100790	"ASCL1, ASH1"	"Achaete-scute complex, Drosophila, homolog-like 1"	ASCL1	429	ENSG00000139352	distal to PAH and proximal to TRA1	"Central hypoventilation syndrome, congenital, 209880 (3), Autosomal dominant; Haddad syndrome, 209880 (3), Autosomal dominant"	Ascl1 (MGI:96919)			
chr12	103746314	103841238	12q22-q23.1	12q23.3		611076	"NT5DC3, TU12B1TY, GNN"	5' nucleotidase domain-containing protein 3	NT5DC3	51559	ENSG00000111696			Nt5dc3 (MGI:3513266)			
chr12	103930333	103947929	12q23.3	12q23.3		191175	"HSP90B1, TRA1, GRP94, GP96"	"Heat-shock protein, 90kD, beta, 1"	HSP90B1	7184	ENSG00000166598			Hsp90b1 (MGI:98817)			
chr12	103965814	103988877	12q24.1	12q23.3		601423	TDG	Thymine-DNA glycosylase	TDG	6996	ENSG00000139372			"Tdg,Tdg-ps (MGI:108247,MGI:3645587)"			
chr12	104064457	104108953	12q23.3	12q23.3		607926	"HCFC2, HCF2"	Host cell factor C2	HCFC2	29915	ENSG00000111727			Hcfc2 (MGI:1915183)			
chr12	104117079	104138261	12q23.3	12q23.3		189904	NFYB	"Transcription factor NF-Y, B subunit"	NFYB	4801	ENSG00000120837			Nfyb (MGI:97317)			
chr12	104215778	104350306	12q23-q24.1	12q23.3		601112	"TXNRD1, TXNR"	Thioredoxin reductase-1	TXNRD1	7296	ENSG00000198431			Txnrd1 (MGI:1354175)			
chr12	104303731	104305204	12q23-q24.1	12q23.3		612986	"EID3, NSMCE4B, NSE4B"	E1A-like inhibitor of differentiation 3	EID3	493861	ENSG00000255150			Eid3 (MGI:1913591)			
chr12	104456913	104762013	12q23	12q23.3		610128	"CHST11, C4ST1"	Carbohydrate sulfotransferase 11	CHST11	50515	ENSG00000171310			Chst11 (MGI:1927166)			
chr12	104802552	104958743	12q23.3	12q23.3		610802	SLC41A2	"Solute carrier family 41, member 2"	SLC41A2	84102	ENSG00000136052			Slc41a2 (MGI:2442940)			
chr12	105019783	105084608	12q23.3	12q23.3		613584	ALDH1L2	"Aldehyde dehydrogenase 1 family, member L2"	ALDH1L2	160428	ENSG00000136010			Aldh1l2 (MGI:2444680)			
chr12	105107713	105169133	12q23.3	12q23.3		615748	"WASHC4, KIAA1033, SWIP, MRT43"	"WASH complex, subunit 4"	WASHC4	23325	ENSG00000136051	mutation identified in 1 MRT43 family	"?Mental retardation, autosomal recessive 43, 615817 (3), Autosomal recessive"	Washc4 (MGI:2441787)			
chr12	105173296	105236229	12q24.1	12q23.3		606231	"APPL2, FLJ10659"	"Adaptor protein, phosphotyrosine interaction, PH domain, and leucine zipper-containing protein 2"	APPL2	55198	ENSG00000136044			Appl2 (MGI:2384914)			
chr12	106063346	106140032	12q23.3	12q23.3		608130	"NUAK1, ARK5,  KIAA0537"	"NUAK family, SNF1-like kinase, 1"	NUAK1	9891	ENSG00000074590			Nuak1 (MGI:1925226)			
chr12	106357657	106510197	12q23.3	12q23.3		614366	"POLR3B, RPC2, C128, HLD8"	"Polymerase III, RNA, subunit B"	POLR3B	55703	ENSG00000013503		"Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism, 614381 (3), Autosomal recessive"	Polr3b (MGI:1917678)			
chr12	106774555	106889315	12q23.3	12q23.3		609147	RIC8B	"Ric8, C. elegans, homolog of, B"	RIC8B	55188	ENSG00000111785			Ric8b (MGI:2682307)			
chr12	106972855	106987165	12q23.3	12q23.3		616929	"MTERF2, MTERFD3"	"Transcription termination factor 2, mitochondrial"	MTERF2	80298	ENSG00000120832			Mterf2 (MGI:1921488)			
chr12	106991363	107093871	12q23-q24.1	12q23.3		601933	"CRY1, PHLL1, DSPD"	Cryptochrome 1 (photolyase-like)	CRY1	1407	ENSG00000008405		"{Delayed sleep phase disorder, susceptibility to}, 614163 (3), Autosomal dominant"	Cry1 (MGI:1270841)			
chr12	107732865	107761271	12q23-q24.1	12q23.3		605780	"PRDM4, PFM1"	PR domain-containing protein 4	PRDM4	11108	ENSG00000110851			Prdm4 (MGI:1920093)			
chr12	108288043	108339346	12q24.1	12q23.3		602351	CMKLR1	Chemokine-like receptor 1	CMKLR1	1240	ENSG00000174600			Cmklr1 (MGI:109603)			
chr12	108522213	108561388	12q24.1	12q23.3		611684	"SART3, P100, KIAA0156, TIP110"	Squamous cell carcinoma antigen recognized by T cells 3	SART3	9733	ENSG00000075856			Sart3 (MGI:1858230)			
chr12	108561462	108569383	12q24.1	12q23.3		611911	"ISCU, HML"	"Iron-sulfur cluster scaffold, E. coli, homolog of"	ISCU	23479	ENSG00000136003		"Myopathy with lactic acidosis, hereditary, 255125 (3), Autosomal recessive"	Iscu (MGI:1913633)			
chr12	108600000	133275309	12q24			612011	CELIAC13	"Celiac disease, susceptibility to, 13"		100188875		associated with rs3184504	"{Celiac disease, susceptibility to, 13}, 612011 (2)"				
chr12	108600000	133275309	12q24			608447	CIMT	Carotid intimal medial thickness		404677		161cM from pter; near SCARB1	"Carotid intimal medial thickness, 608447 (2)"				
chr12	108600000	133275309	12q24			607411	PDA1	Patent ductus arteriosus		100996949			"{Patent ductus arteriosus, susceptibility to}, 607411 (2), Autosomal recessive"				
chr12	108600000	120300000	12q24.1-q24.2			175850	"POROK2, PPPD1"	"Porokeratosis 2, palmar, plantar, and disseminated"		100196910		between D12S1613 and D12S1341	"Porokeratosis 2, palmar, plantar, and disseminated, 175850 (2), Autosomal dominant"				
chr12	108600000	133275309	12q24			608437	SLEB4	"Systemic lupus erythematosus, susceptibility to, 4"		404714			"{Systemic lupus erythematosus, susceptibility to, 4}, 608437 (2)"				
chr12	108600000	113900000	12q24.1			609261	STUT2	"Stuttering, familial persistent, 2"		100049543		max lod with PAH	"Stuttering, familial persistent, 2, 609261 (2)"				
chr12	108621894	108633893	12q24	12q24.11		600738	"SELPLG, PSGL1"	Selectin P ligand	SELPLG	6404	ENSG00000110876			Selplg (MGI:106689)			
chr12	108645108	108759954	12q24.1	12q24.11		605269	CORO1C	Coronin 1C	CORO1C	23603	ENSG00000110880			Coro1c (MGI:1345964)			
chr12	108782689	108857605	12q24.11	12q24.11		606778	"SSH1, KIAA1298"	"Slingshot, Drosophila, homolog of, 1"	SSH1	54434	ENSG00000084112			Ssh1 (MGI:2686240)			
chr12	108880029	108901042	12q24	12q24.11		124050	"DAO, DAMOX"	D-amino-acid oxidase	DAO	1610	ENSG00000110887	tightly linked to SCA2	"{Schizophrenia}, 181500 (2), Autosomal dominant"	Dao (MGI:94859)			
chr12	108908128	109021239	12q24.1	12q24.11		611699	SVOP	SV2-related protein	SVOP	55530	ENSG00000166111			Svop (MGI:1915916)			
chr12	109023088	109088025	12q23-q24	12q24.11		612492	USP30	Ubiquitin-specific protease 30	USP30	84749	ENSG00000135093			Usp30 (MGI:2140991)			
chr12	109088187	109093630	12q23.3	12q24.11		610602	"ALKBH2, ABH2"	"AlkB, E. coli, homolog of, 2"	ALKBH2	121642	ENSG00000189046			Alkbh2 (MGI:2141032)			
chr12	109097593	109110992	12q23-q24.1	12q24.11		191525	"UNG, DGU, HIGM5"	Uracil-DNA glycosylase	UNG	7374	ENSG00000076248		"Immunodeficiency with hyper IgM, type 5, 608106 (3), Autosomal recessive"	Ung (MGI:109352)			
chr12	109112665	109268225	12q24.1	12q24.11		601557	"ACACB, ACCB, ACC2"	"Acetyl-Coenzyme A carboxylase, beta"	ACACB	32	ENSG00000076555			Acacb (MGI:2140940)			
chr12	109277977	109309405	12q24.1	12q24.11		609429	FOXN4	Forkhead box N4	FOXN4	121643	ENSG00000139445			Foxn4 (MGI:2151057)			
chr12	109388276	109448370	12q24.11	12q24.11		614636	MYO1H	Myosin IH	MYO1H	283446	ENSG00000174527			Myo1h (MGI:1914674)			
chr12	109448654	109477543	12q24.11	12q24.11		613421	KCTD10	Potassium channel tetramerization domain-containing 10	KCTD10	83892	ENSG00000110906			Kctd10 (MGI:2141207)			
chr12	109477409	109543627	12q24.11	12q24.11		608047	"UBE3B, BPIDS, KOS"	Ubiquitin-protein ligase E3B	UBE3B	89910	ENSG00000151148		"Kaufman oculocerebrofacial syndrome, 244450 (3), Autosomal recessive"	Ube3b (MGI:1891295)			
chr12	109553714	109573579	12q24	12q24.11		607568	MMAB	MMAB gene	MMAB	326625	ENSG00000139428		"Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type, 251110 (3), Autosomal recessive"	Mmab (MGI:1924947)			
chr12	109573460	109597269	12q24	12q24.11		251170	"MVK, MVLK, POROK3"	Mevalonate kinase	MVK	4598	ENSG00000110921		"Hyper-IgD syndrome, 260920 (3), Autosomal recessive; Mevalonic aciduria, 610377 (3), Autosomal recessive; Porokeratosis 3, multiple types, 175900 (3), Autosomal dominant"	Mvk (MGI:107624)			
chr12	109783086	109833406	12q24.1	12q24.11		605427	"TRPV4, VROAC, HMSN2C, CMT2C, SPSMA, SSQTL1, SMAL, BCYM3"	"Transient receptor potential cation channel, subfamily V, member 4 (vanilloid receptor-related osmotically activated channel)"	TRPV4	59341	ENSG00000111199	mutation identified in 1 ANFH2 family	"?Avascular necrosis of femoral head, primary, 2, 617383 (3), Autosomal dominant; Brachyolmia type 3, 113500 (3), Autosomal dominant; Digital arthropathy-brachydactyly, familial, 606835 (3), Autosomal dominant; Hereditary motor and sensory neuropathy, type IIc, 606071 (3), Autosomal dominant; Metatropic dysplasia, 156530 (3), Autosomal dominant; Parastremmatic dwarfism, 168400 (3), Autosomal dominant; SED, Maroteaux type, 184095 (3), Autosomal dominant; Scapuloperoneal spinal muscular atrophy, 181405 (3), Autosomal dominant; [Sodium serum level QTL 1], 613508 (3); Spinal muscular atrophy, distal, congenital nonprogressive, 600175 (3), Autosomal dominant; Spondylometaphyseal dysplasia, Kozlowski type, 184252 (3), Autosomal dominant"	Trpv4 (MGI:1926945)			
chr12	109850942	109880487	12q24.11	12q24.11		608949	GLTP	Glycolipid transfer protein	GLTP	51228	ENSG00000139433			Gltp (MGI:1929253)			
chr12	109880666	109918068	12q24.1	12q24.11		612654	TCHP	Trichoplein	TCHP	84260	ENSG00000139437			Tchp (MGI:1925082)			
chr12	109999168	110039431	12q24.11	12q24.11		615123	ANKRD13A	Ankyrin repeat domain-containing protein 13A	ANKRD13A	88455	ENSG00000076513			Ankrd13a (MGI:1915670)			
chr12	110124334	110218794	12q24.13	12q24.11		605489	"IFT81, DV1, CDV1R, SRTD19"	"Intraflagellar transport 81, Chlamydomonas, homolog of"	IFT81	28981	ENSG00000122970		"Short-rib thoracic dysplasia 19 with or without polydactyly 19, 617895 (3), Autosomal recessive"	Ift81 (MGI:1098597)			
chr12	110281226	110351092	12q23-q24.1	12q24.11		108740	"ATP2A2, ATP2B, DAR"	"ATPase, Ca++ transporting, slow-twitch, cardiac muscle-2"	ATP2A2	488	ENSG00000174437		"Acrokeratosis verruciformis, 101900 (3), Autosomal dominant; Darier disease, 124200 (3), Autosomal dominant"	Atp2a2 (MGI:88110)			
chr12	110372899	110403729	12q24.11	12q24.11		606949	"ANAPC7, APC7"	"Anaphase-promoting complex, subunit 7"	ANAPC7	51434	ENSG00000196510			Anapc7 (MGI:1929711)			
chr12	110434889	110450410	12q24.11	12q24.11		604225	"ARPC3, ARC21"	"Actin-related protein 2/3 complex, subunit 3"	ARPC3	10094	ENSG00000111229			Arpc3 (MGI:1928375)			
chr12	110501650	110534631	12q24	12q24.11		608368	RAD9B	"RAD9, S. pombe, homolog of, A"	RAD9B	144715	ENSG00000151164			Rad9b (MGI:2385231)			
chr12	110533244	110583258	12q24.1	12q24.11		609668	"PPTC7, TAPP2C"	"PTC7 protein phosphatase, S. cerevisiae, homolog of"	PPTC7	160760	ENSG00000196850			Pptc7 (MGI:2444593)			
chr12	110614026	110649129	12q24.1	12q24.11		609863	"TECT1, JBTS13"	"Tectonic family, member 1"	TCTN1	79600	ENSG00000204852		"Joubert syndrome 13, 614173 (3), Autosomal recessive"	Tctn1 (MGI:3603820)			
chr12	110648685	110704944	12q24.11	12q24.11		611227	"HVCN1, HV1, VSOP"	Hydrogen voltage-gated channel 1	HVCN1	84329	ENSG00000122986			Hvcn1 (MGI:1921346)			
chr12	110708368	110742977	12q24.1-q24.2	12q24.11		176914	PPP1CC	"Protein phosphatase-1, catalytic subunit, gamma isoform"	PPP1CC	5501	ENSG00000186298			Gm5601 (MGI:3647492)			
chr12	110910818	110920599	12q23-q24.3	12q24.11		160781	"MYL2, CMH10"	"Myosin, light polypeptide-2, regulatory, cardiac, slow"	MYL2	4633	ENSG00000111245		"Cardiomyopathy, hypertrophic, 10, 608758 (3), Autosomal dominant"	Myl2 (MGI:97272)			
chr12	111360650	111369120	12q24.12	12q24.12		614239	"FAM109A, SES1, IPIP27A"	"Family with sequence similarity 109, member A"	PHETA1	144717	ENSG00000198324			Fam109a (MGI:2442708)			
chr12	111405106	111451622	12q24	12q24.12		605093	"SH2B3, LNK"	SH2B adaptor protein 3	SH2B3	10019	ENSG00000111252		"Erythrocytosis, somatic, 133100 (3); Myelofibrosis, somatic, 254450 (3); Thrombocythemia, somatic, 187950 (3)"	Sh2b3 (MGI:893598)			
chr12	111452213	111599675	12q24	12q24.12		601517	"ATXN2, ATX2, SCA2, ASL13"	Ataxin-2	ATXN2	6311	ENSG00000204842		"{Amyotrophic lateral sclerosis, susceptibility to, 13}, 183090 (3), Autosomal dominant; {Parkinson disease, late-onset, susceptibility to}, 168600 (3), Isolated cases, Multifactorial; Spinocerebellar ataxia 2, 183090 (3), Autosomal dominant"	Atxn2 (MGI:1277223)			
chr12	111642145	111686022	12q24	12q24.12		604986	"BRAP, BRAP2, IMP"	BRCA1-associated protein	BRAP	8315	ENSG00000089234			Brap (MGI:1919649)			
chr12	111686052	111757106	12q24.1	12q24.12		611181	ACAD10	"Acyl-CoA dehydrogenase family, member 10"	ACAD10	80724	ENSG00000111271			Acad10 (MGI:1919235)			
chr12	111766886	111809984	12q24.2	12q24.12		100650	ALDH2	"Aldehyde dehydrogenase 2 family, mitochondrial"	ALDH2	217	ENSG00000111275		"Alcohol sensitivity, acute, 610251 (3), Autosomal dominant; {Esophageal cancer, alcohol-related, susceptibility to} (3); {Hangover, susceptibility to}, 610251 (3), Autosomal dominant; {Sublingual nitroglycerin, susceptibility to poor response to} (3)"	Aldh2 (MGI:99600)			
chr12	111841977	111902224	12q24.12-q24.13	12q24.12-q24.13		606723	"MAPKAPK5, PRAK"	Mitogen-activated protein kinase-activated protein kinase 5	MAPKAPK5	8550	ENSG00000089022			Mapkapk5 (MGI:1333110)			
chr12	112013339	112023219	Chr.12	12q24.13		602287	"C12orf8, ERP28, ERP29"	Endoplasmic reticulum lumenal protein 28	ERP29	10961	ENSG00000089248			Erp29 (MGI:1914647)			
chr12	112026688	112108830	12q24.13	12q24.13		612755	"MDM20, C12orf30"	"Mitochondrial distribution and morphology 20, yeast, homolog of"	NAA25	80018	ENSG00000111300			Naa25 (MGI:2442563)			
chr12	112125544	112153603	12q24.13	12q24.13		613197	"TRAFD1, FLN29"	TRAF-type zinc finger domain-containing 1	TRAFD1	10906	ENSG00000135148			Trafd1 (MGI:1923551)			
chr12	112405180	112418849	12q	12q24.13		603703	RPL6	Ribosomal protein L6	RPL6	6128	ENSG00000089009			"Rpl6l,Rpl6 (MGI:108057,MGI:3647789)"			
chr12	112418897	112509917	12q24.1	12q24.13		176876	"PTPN11, PTP2C, SHP2, NS1, JMML, METCDS"	"Protein tyrosine phosphatase, nonreceptor-type, 11"	PTPN11	5781	ENSG00000179295		"LEOPARD syndrome 1, 151100 (3), Autosomal dominant; Leukemia, juvenile myelomonocytic, somatic, 607785 (3); Metachondromatosis, 156250 (3), Autosomal dominant; Noonan syndrome 1, 163950 (3), Autosomal dominant"	Ptpn11 (MGI:99511)			
chr12	112575096	112898880	12q24.1	12q24.13		612159	"RPH3A, KIAA0985"	Rabphilin 3A	RPH3A	22895	ENSG00000089169			Rph3a (MGI:102788)			
chr12	112906776	112932189	12q24.2	12q24.13		164350	"OAS1, OIAS"	"2',5'-oligoadenylate synthetase-1"	OAS1	4938	ENSG00000089127		"{Diabetes mellitus, type 1, susceptibility to}, 222100 (3), Autosomal recessive; {Viral infection, susceptibility to} (3)"	"Oas1g,Oas1a (MGI:2180860,MGI:97429)"			
chr12	112938432	112973250	12q24.2	12q24.13		603351	OAS3	"2',5'-oligoadenylate synthetase-3"	OAS3	4940	ENSG00000111331			Oas3 (MGI:2180850)			
chr12	112978465	113011722	12q24.2	12q24.13		603350	OAS2	"2',5'-oligoadenylate synthetase-2"	OAS2	4939	ENSG00000111335			Oas2 (MGI:2180852)			
chr12	113056710	113098027	12q24	12q24.13		602582	DTX1	"Deltex, Drosophila, homolog of, 1"	DTX1	1840	ENSG00000135144			Dtx1 (MGI:1352744)			
chr12	113096514	113136247	12q23-q24	12q24.13		604118	"RASAL1, RASAL"	Ras protein activator-like 1	RASAL1	8437	ENSG00000111344			Rasal1 (MGI:1330842)			
chr12	113157172	113185478	12q22-q23	12q24.13		611665	"DDX54, DP97"	Dead/H Box 54	DDX54	79039	ENSG00000123064			Ddx54 (MGI:1919240)			
chr12	113221428	113298588	12q24.1	12q24.13		609666	"TPCN1, TPC1, KIAA1169"	Two-pore segment channel 1	TPCN1	53373	ENSG00000186815			Tpcn1 (MGI:2182472)			
chr12	113298765	113335167	12q24	12q24.13		609841	"SLC8B1, SLC24A6, NCKX6"	Solute carrier family 8 member B1	SLC8B1	80024	ENSG00000089060			Slc8b1 (MGI:2180781)			
chr12	113392444	113403886	12q24.13	12q24.13		182128	"SDS, SDH"	Serine dehydratase	SDS	10993	ENSG00000135094			Sds (MGI:98270)			
chr12	113462888	113472071	12q24.31-q24.32	12q24.13		605992	LHX5	LIM homeo box protein 5	LHX5	64211	ENSG00000089116			Lhx5 (MGI:107792)			
chr12	113816737	113966370	12q24.13-q24.21	12q24.13-q24.21		616444	"RBM19, KIAA0682"	RNA-binding motif protein 19	RBM19	9904	ENSG00000122965			Rbm19 (MGI:1921361)			
chr12	113900000	133275309	12q24.2-q24.3			614422	"CTRCT37, CCA5"	Cataract 37		100861439		between D12S1718 and D12S1723	"Cataract 37, autosomal dominant, 614422 (2), Autosomal dominant"				
chr12	113900000	120300000	12q24.2			601407	NIDDM2	"Diabetes mellitus, noninsulin-dependent, 2"	NIDDM2	4813		no mutations found in HNF1A	"Diabetes mellitus, noninsulin-dependent, 2, 601407 (2)"				
chr12	113900000	133275309	12q24.2-q24.3			603416	"RPL21P1, ALFN1, HALF1"	Ribosomal protein L21 pseudogene 1	RPL21P1	6145							
chr12	114353910	114408707	12q24.1	12q24.21		601620	TBX5	T-box 5	TBX5	6910	ENSG00000089225		"Holt-Oram syndrome, 142900 (3), Autosomal dominant"	Tbx5 (MGI:102541)			
chr12	114670253	114684163	12q24.1	12q24.21		601621	TBX3	T-box 3	TBX3	6926	ENSG00000135111		"Ulnar-mammary syndrome, 181450 (3), Autosomal dominant"	Tbx3 (MGI:98495)			
chr12	115958575	116277218	12q24	12q24.21		608771	"MED13L, THRAP2, PROSIT240, TRAP240L, KIAA1025, MRFACD"	Mediator complex subunit 13-like	MED13L	23389	ENSG00000123066		"Mental retardation and distinctive facial features with or without cardiac defects, 616789 (3), Autosomal dominant; Transposition of the great arteries, dextro-looped 1, 608808 (3), Autosomal dominant"	Med13l (MGI:2670178)			
chr12	116856143	116881426	12q24.2	12q24.22		603447	"HRK, DP5"	Harakiri	HRK	8739	ENSG00000135116						
chr12	116910948	117032497	12q24.23	12q24.22		609073	"FBXW8, FBW8, FBXW6, FBW6, FBXO29, FBX29"	F-box and WD40 domain protein 8	FBXW8	26259	ENSG00000174989			Fbxw8 (MGI:1923041)			
chr12	117038922	117099489	12q24.2	12q24.22		611585	"TESC, TSC"	"Tescalcin, mouse, homolog of"	TESC	54997	ENSG00000088992			Tesc (MGI:1930803)			
chr12	117143472	117190494	12q24.23	12q24.22		609095	"FBXO21, FBX21, KIAA0875"	F-box only protein 21	FBXO21	23014	ENSG00000135108			Fbxo21 (MGI:1924223)			
chr12	117208141	117361801	12q24.2-q24.31	12q24.22		163731	NOS1	"Nitric oxide synthase 1, neuronal"	NOS1	4842	ENSG00000089250			Nos1 (MGI:97360)			
chr12	117453011	117968556	12q24.2	12q24.22-q24.23		610737	KSR2	Kinase suppressor of RAS 2	KSR2	283455	ENSG00000171435			Ksr2 (MGI:3610315)			
chr12	118016660	118033563	12q24.2-q24.3	12q24.23		600407	RFC5	"Replication factor C5, 36.5kD (activator 1, 36.5kD)"	RFC5	5985	ENSG00000111445			Rfc5 (MGI:1919401)			
chr12	118135883	118145587	12q24.23	12q24.23		604591	"PEBP1, PBP, RKIP"	Phosphatidylethanolamine-binding protein 1	PEBP1	5037	ENSG00000089220			Pebp1 (MGI:1344408)			
chr12	118149800	118372949	12q24.23	12q24.23		616711	"TAOK3, JIK, DPK"	TAO kinase 3	TAOK3	51347	ENSG00000135090			Taok3 (MGI:3041177)			
chr12	118981494	119163050	12q24.23	12q24.23		613103	"SRRM4, KIAA1853, NSR100"	Serine/arginine repetitive matrix protein 4	SRRM4	84530	ENSG00000139767			Srrm4 (MGI:1916205)			
chr12	119178789	119194745	12q24	12q24.23		608014	"HSPB8, H11, E2IG1, DHMN2, CMT2L, HMN2A"	Heat-shock 22-kD protein 8	HSPB8	26353	ENSG00000152137		"Charcot-Marie-Tooth disease, axonal, type 2L, 608673 (3), Autosomal dominant; Neuropathy, distal hereditary motor, type IIA, 158590 (3), Autosomal dominant"	Hspb8 (MGI:2135756)			
chr12	119667863	119681623	12q24.1	12q24.23		602740	PRKAB1	"Protein kinase, AMP-activated, noncatalytic, beta-1"	PRKAB1	5564	ENSG00000111725			Prkab1 (MGI:1336167)			
chr12	119685789	119877317	12q24.1-q24.3	12q24.23		605629	"CIT, STK21, CRIK, MCPH17"	Citron rho-interacting serine/threonine kinase	CIT	11113	ENSG00000122966		"Microcephaly 17, primary, autosomal recessive, 617090 (3), Autosomal recessive"	Cit (MGI:105313)			
chr12	119989805	120094494	12q24.23	12q24.23		617002	"BICDL1, BICDR1, CCDC64"	BICD family-like cargo adaptor 1	BICDL1	92558	ENSG00000135127			Bicdl1 (MGI:1922915)			
chr12	120095093	120117468	12q24.23	12q24.23		604199	RAB35	Ras-associated protein Rab35	RAB35	11021	ENSG00000111737			Rab35 (MGI:1924657)			
chr12	120127209	120194709	12q24.2	12q24.23		605614	GCN1L1	"General control of amino acid synthesis 1, yeast, homolog-like 1"	GCN1	10985	ENSG00000089154			Gcn1l1 (MGI:2444248)			
chr12	120196699	120201210	Chr.12	12q24.23		180510	RPLP0	"Ribosomal phosphoprotein, large, P0"	RPLP0	6175	ENSG00000089157			Rplp0 (MGI:1927636)			
chr12	120210438	120265770	12q24	12q24.23		602505	PXN	Paxillin	PXN	5829	ENSG00000089159			Pxn (MGI:108295)			
chr12	120290638	120313241	12q24.31	12q24.23-q24.31		604482	"SIRT4, SIR2L4"	"Sirtuin, S. cerevisiae, homolog 4"	SIRT4	23409	ENSG00000089163			Sirt4 (MGI:1922637)			
chr12	120300000	125400000	12q24.31			612573	MPVQTL1	Mean platelet volume quantitative trait locus 1		100271867		associated with rs7961894	"[Mean platelet volume QTL1], 612573 (2)"				
chr12	120322110	120327788	12q23-q24.1	12q24.31		172410	"PLA2G1B, PLA2A, PLA2, PPLA2"	"Phospholipase A2, group IB, pancreas"	PLA2G1B	5319	ENSG00000170890			Pla2g1b (MGI:101842)			
chr12	120339661	120369179	12q24.1-q24.31	12q24.31		603328	MSI1	"Musashi, Drosophila, homolog of, 1"	MSI1	4440	ENSG00000135097			Msi1 (MGI:107376)			
chr12	120438089	120440741	12q24.2	12q24.31		602072	"COX6A1, CMTRID"	"Cytochrome c oxidase, subunit VIa, polypeptide-1"	COX6A1	1337	ENSG00000111775	pseudogenes on chr.7 and chr.6	"Charcot-Marie-Tooth disease, recessive intermediate D, 616039 (3), Autosomal recessive"	Cox6a1 (MGI:103099)			
chr12	120443960	120446411	12q24.31	12q24.31		614943	"TRIAP1, HSPC132"	TP53-regulated inhibitor of apoptosis 1	TRIAP1	51499	ENSG00000170855			Triap1 (MGI:1916326)			
chr12	120446437	120463752	12q24.31	12q24.31		617210	GATC	"Glutamyl-tRNA amidotransferase, subunit C"	GATC	283459	ENSG00000257218			Gatc (MGI:1923776)			
chr12	120461667	120469754	12q24.31	12q24.31		601943	"SRSF9, SFRS9, SRp30c"	"Splicing factor, serine/arginine-rich, 9"	SRSF9	8683	ENSG00000111786			Srsf9 (MGI:104896)			
chr12	120469856	120498494	12q24.2	12q24.31		601562	"DYNLL1, DNCL1, DLC1, PIN"	"Dynein, light chain, LC8-type 1"	DYNLL1	8655	ENSG00000088986	possible pseudogene on 14q24		Dynll1 (MGI:1861457)			
chr12	120490337	120495945	12q24.31	12q24.31		616207	"NRAV, DYNLL1AS1"	"Negative regulator of antiviral response, noncoding"	NRAV	100506668		overlaps intron 1 of DYNLL1 in antisense orientation					
chr12	120503278	120534612	12q24.31	12q24.31		616359	COQ5	"Coq5, S. cerevisiae, homolog of"	COQ5	84274	ENSG00000110871			Coq5 (MGI:1098643)			
chr12	120534328	120577593	12q24.31	12q24.31		615998	"RNF10, KIAA0262"	RING finger protein 10	RNF10	9921	ENSG00000022840			Rnf10 (MGI:1859162)			
chr12	120579044	120581451	12q24.31	12q24.31		609992	"POP5, HSPC004"	"Processing of precursor 5, S. cerevisiae, homolog of"	POP5	51367	ENSG00000167272			Pop5 (MGI:2151221)			
chr12	120687123	120701863	12q24.31	12q24.31		613802	"MLEC, KIAA0152"	Malectin	MLEC	9761	ENSG00000110917			Mlec (MGI:1924015)			
chr12	120725737	120740007	12q22-qter	12q24.31		606885	"ACADS, SCAD"	"Acyl-Coenzyme A dehydrogenase, C-2 to C-3 short chain"	ACADS	35	ENSG00000122971		"Acyl-CoA dehydrogenase, short-chain, deficiency of, 201470 (3), Autosomal recessive"	Acads (MGI:87868)			
chr12	120762509	120904351	12q24.31	12q24.31		608240	"SPPL3, IMP2"	Signal peptide peptidase-like 3	SPPL3	121665	ENSG00000157837			Sppl3 (MGI:1891433)			
chr12	120977682	121002511	12q24.2	12q24.31		142410	"HNF1A, TCF1, MODY3, IDDM20"	HNF1 homeobox B	HNF1A	6927	ENSG00000135100		"Diabetes mellitus, insulin-dependent, 20, 612520 (3); {Diabetes mellitus, insulin-dependent}, 222100 (3), Autosomal recessive; {Diabetes mellitus, noninsulin-dependent, 2}, 125853 (3), Autosomal dominant; Hepatic adenoma, somatic, 142330 (3); MODY, type III, 600496 (3), Autosomal dominant; Renal cell carcinoma, 144700 (3)"	Hnf1a (MGI:98504)			
chr12	121018881	121039241	12q24.2	12q24.31		603281	"OASL, TRIP14"	"2',5'-oligoadenylate synthetase-like"	OASL	8638	ENSG00000135114			Oasl1 (MGI:2180849)			
chr12	121132818	121188031	12q24	12q24.31		602566	"P2RX7, P2X7"	"Purinergic receptor P2X, ligand-gated ion channel, 7"	P2RX7	5027	ENSG00000089041			P2rx7 (MGI:1339957)			
chr12	121209860	121234105	12q24.32	12q24.31		600846	"P2RX4, P2X4"	"Purinergic receptor P2X, ligand-gated ion channel, 4"	P2RX4	5025	ENSG00000135124			P2rx4 (MGI:1338859)			
chr12	121237691	121298307	12q24.2	12q24.31		615002	"CAMKK2, KIAA0787, CAMKKB"	"Calcium/calmodulin-dependent protein kinase kinase 2, beta"	CAMKK2	10645	ENSG00000110931			Camkk2 (MGI:2444812)			
chr12	121308244	121354208	Chr.12	12q24.31		606948	"ANAPC5, APC5"	"Anaphase-promoting complex, subunit 5"	ANAPC5	51433	ENSG00000089053			Anapc5 (MGI:1929722)			
chr12	121400082	121424351	12q23-q24.1	12q24.31		608299	"RNF34, RFI"	Ring finger protein 34	RNF34	80196	ENSG00000170633			Rnf34 (MGI:2153340)			
chr12	121402287	121582267	12q24.31	12q24.31		609078	"KDM2B, FBXL10, FBL10, CXXC2, JHDM1B"	Lysine-specific demethylase 2B	KDM2B	84678	ENSG00000089094			Kdm2b (MGI:1354737)			
chr12	121626549	121642039	12q24	12q24.31		610277	"ORAI1, TMEM142A, CRACM1, IMD9, TAM2"	ORAI calcium release-activated calcium modulator 1	ORAI1	84876	ENSG00000276045		"Immunodeficiency 9, 612782 (3), Autosomal recessive; Myopathy, tubular aggregate, 2, 615883 (3), Autosomal dominant"	Orai1 (MGI:1925542)			
chr12	121712751	121782067	12q24.31	12q24.31		616551	TMEM120B	Transmembrane protein 120B	TMEM120B	144404	ENSG00000188735			Tmem120b (MGI:3603158)			
chr12	121803664	121832655	12q24.31	12q24.31		611055	"SETD1B, SET1B, KIAA1076"	SET domain-containing protein 1B	SETD1B	23067	ENSG00000139718						
chr12	121839526	121888610	12q24-qter	12q24.31		609695	HPD	4-hydroxyphenylpyruvate dioxygenase	HPD	3242	ENSG00000158104		"Hawkinsinuria, 140350 (3), Autosomal dominant; Tyrosinemia, type III, 276710 (3), Autosomal recessive"	Hpd (MGI:96213)			
chr12	121888730	121917864	12q24.2-q24.3	12q24.31		603146	PSMD9	"Proteasome 26S subunit, non-ATPase, 9"	PSMD9	5715	ENSG00000110801			Psmd9 (MGI:1914401)			
chr12	122021885	122062043	12q24.1	12q24.31		601406	"BCL7A, BCL7"	B-cell CLL/lymphoma-7A	BCL7A	605	ENSG00000110987		"B-cell non-Hodgkin lymphoma, high-grade (3)"	Bcl7a (MGI:1924295)			
chr12	122078727	122147346	12q21.31	12q24.31		608090	"MLXIP, MONDOA, KIAA0867"	MLX-interacting protein	MLXIP	22877	ENSG00000175727			Mlxip (MGI:2141183)			
chr12	122172029	122174198	12q24.31	12q24.31		609509	IL31	Interleukin 31	IL31	386653	ENSG00000204671						
chr12	122203680	122208951	12q24.31	12q24.31		605864	B3GNT4	"Beta-1,3-N-acetylglucosaminyltransferase 4"	B3GNT4	79369	ENSG00000176383			B3gnt4 (MGI:2680208)			
chr12	122207661	122227533	12q24.31	12q24.31		605219	"SMAC, DIABLO, DFNA64"	Second mitochondria-derived activator of caspase	DIABLO	56616	ENSG00000184047		"Deafness, autosomal dominant 64, 614152 (3), Autosomal dominant"	Diablo (MGI:1913843)			
chr12	122229560	122266822	12q24.31	12q24.31		610034	"VPS33A, MPSPS"	"Vacuolar protein sorting 33, yeast, homolog of, A"	VPS33A	65082	ENSG00000139719		"Mucopolysaccharidosis-plus syndrome, 617303 (3), Autosomal recessive"	Vps33a (MGI:1924823)			
chr12	122271431	122422955	12q24.3	12q24.31		179838	"CLIP1, RSN, CYLN1, CLIP170"	CAP-GLY domain containing linker protein 1	CLIP1	6249	ENSG00000130779			Clip1 (MGI:1928401)			
chr12	122471598	122501183	12q24.31	12q24.31		616381	ZCCHC8	Zinc finger CCHC domain-containing protein 8	ZCCHC8	55596	ENSG00000033030			Zcchc8 (MGI:1917900)			
chr12	122527105	122626408	12q24.31	12q24.31		607363	"KNTC1, ROD, KIAA0166"	Kinetochore-associated protein 1	KNTC1	9735	ENSG00000184445	previously assigned to chr.17		Kntc1 (MGI:2673709)			
chr12	122701292	122703356	12q24.31	12q24.31		609163	"HCAR2, GPR109A, HM74A"	Hydroxycarboxylic acid receptor 2	HCAR2	338442	ENSG00000182782			Hcar2 (MGI:1933383)			
chr12	122714755	122716891	12q24.31	12q24.31		606039	"HCAR3, GPR109B, HM74, PUMAG"	Hydroxycarboxylic acid receptor 3	HCAR3	8843	ENSG00000255398						
chr12	122727605	122730581	12q24.31	12q24.31		606923	"HCAR1, GPR81, TAGPCR"	Hydroxycarboxylic acid receptor 1	HCAR1	27198	ENSG00000196917			Hcar1 (MGI:2441671)			
chr12	122752820	122771063	12q24.31	12q24.31		604550	"DENR, DRP"	Density-regulated protein	DENR	8562	ENSG00000139726			Denr (MGI:1915434)			
chr12	122773620	122827384	12q24.31	12q24.31		613481	"CCDC62, ERAP75"	Coiled-coil domain-containing protein 62	CCDC62	84660	ENSG00000130783			Ccdc62 (MGI:2684996)			
chr12	122834497	122862960	12q24.2-q24.3	12q24.31		605613	"HIP1R, HIP12"	Huntingtin-interacting protein 1-related protein	HIP1R	9026	ENSG00000130787			Hip1r (MGI:1352504)			
chr12	122865327	122896164	12q24.31	12q24.31		610037	VPS37B	"Vacuolar protein sorting 37, yeast, homolog of, B"	VPS37B	79720	ENSG00000139722			Vps37b (MGI:1916724)			
chr12	122917323	122975159	12q24	12q24.31		605453	ABCB9	"ATP-binding cassette, subfamily B, member 9"	ABCB9	23457	ENSG00000150967			Abcb9 (MGI:1861729)			
chr12	122980059	122982912	12q24.31	12q24.31		607668	ARL6IP4	ADP-ribosylation-like factor 6 interacting protein 4	ARL6IP4	51329	ENSG00000182196			Arl6ip4 (MGI:1929500)			
chr12	123233296	123257958	12q24.31	12q24.31		613541	"C12orf65, COXPD7, SPG55"	Chromosome 12 open reading frame 65	C12orf65	91574	ENSG00000130921		"Combined oxidative phosphorylation deficiency 7, 613559 (3), Autosomal recessive; Spastic paraplegia 55, autosomal recessive, 615035 (3), Autosomal recessive"	2810006K23Rik (MGI:1919900)			
chr12	123152323	123244013	Chr.12	12q24.31		605501	"MPHOSPH9, MPP9"	M-phase phosphoprotein 9	MPHOSPH9	10198	ENSG00000051825			Mphosph9 (MGI:2443138)			
chr12	123260969	123272315	12q24.31	12q24.31		602198	"CDK2AP1, DOC1"	CDK-associated protein 1 (deleted in oral cancer-1)	CDK2AP1	8099	ENSG00000111328			Cdk2ap1 (MGI:1202069)			
chr12	123289108	123365208	12q24.31	12q24.31		614274	SBNO1	"Strawberry notch, Drosophila, homolog of, 1"	SBNO1	55206	ENSG00000139697			Sbno1 (MGI:2384298)			
chr12	123409889	123436732	12q24.31	12q24.31		614093	"RILPL2, RLP2"	RAB-interacting lysosomal protein-like 2	RILPL2	196383	ENSG00000150977			Rilpl2 (MGI:1933112)			
chr12	123471072	123533717	12q24.31	12q24.31		614092	"RILPL1, RLP1, GOSPEL"	RAB-interacting lysosomal protein-like 1	RILPL1	353116	ENSG00000188026			Rilpl1 (MGI:1922945)			
chr12	123621022	123633775	12q24.31	12q24.31		606686	"EIF2B1, EIF2BA"	"Eukaryotic translation initiation factor 2B, subunit 1"	EIF2B1	1967	ENSG00000111361		"Leukoencephalopathy with vanishing white matter, 603896 (3), Autosomal recessive"	Eif2b1 (MGI:2384802)			
chr12	123633738	123662603	12q24.31	12q24.31		601750	"GTF2H3, TFB4"	"General transcription factor IIH, polypeptide 3"	GTF2H3	2967	ENSG00000111358			Gtf2h3 (MGI:1277143)			
chr12	123671107	123708404	12q24.31	12q24.31		613846	"TCTN2, TECT2, MKS8, JBTS24"	"Tectonic family, member 2"	TCTN2	79867	ENSG00000168778	mutation identified in 1 MKS8 family	"Joubert syndrome 24, 616654 (3), Autosomal recessive; ?Meckel syndrome 8, 613885 (3), Autosomal recessive"	Tctn2 (MGI:1915228)			
chr12	123712317	123761754	12q24.3	12q24.31		611716	"ATP6V0A2, WSS, ARCL2A"	"ATPase, H+ transporting, lysosomal, V0 subunit A2"	ATP6V0A2	23545	ENSG00000185344		"Cutis laxa, autosomal recessive, type IIA, 219200 (3), Autosomal recessive; Wrinkly skin syndrome, 278250 (3), Autosomal recessive"	Atp6v0a2 (MGI:104855)			
chr12	123761994	123935719	12q24.31	12q24.31		605884	DNAH10	"Dynein, axonemal, heavy chain 10"	DNAH10	196385	ENSG00000197653	previously assigned to 13q14		Dnah10 (MGI:1860299)			
chr12	123973214	124015438	12q24.2	12q24.31		617890	"ZNF664, ZFOC1"	Zinc finger protein 664	ZNF664	144348	ENSG00000179195			Zfp664 (MGI:2442505)			
chr12	124289163	124316023	12q24.31	12q24.31		615927	"FAM101A, CFM2"	"Family with sequence similarity 101, member A"	RFLNA	144347	ENSG00000178882			Rflna (MGI:1920371)			
chr12	124324410	124567463	12q24	12q24.31		600848	"NCOR2, SMRT"	Nuclear receptor corepressor 2	NCOR2	9612	ENSG00000196498			Ncor2 (MGI:1337080)			
chr12	124777627	124863972	12q24.31	12q24.31		601040	"SCARB1, CD36L1, CLA1, HDLQTL6"	"Scavenger receptor class B, member 1 (CD36 antigen-like 1)"	SCARB1	949	ENSG00000073060		"[High density lipoprotein cholesterol level QTL6], 610762 (3)"	Scarb1 (MGI:893578)			
chr12	124911644	124915040	12q24.3	12q24.31		191340	UBC	Ubiquitin C	UBC	7316	ENSG00000150991			Ubc (MGI:98889)			
chr12	124946823	124989124	12q24.31	12q24.31		617362	"DHX37, KIAA1517"	DEAH box polypeptide 37	DHX37	57647	ENSG00000150990			Dhx37 (MGI:3028576)			
chr12	124993647	125051844	12q24.31	12q24.31		615627	BRI3BP	BRI3-binding protein	BRI3BP	140707	ENSG00000184992			Bri3bp (MGI:1924059)			
chr12	125025442	125027422	12q24.31	12q24.31		615622	"THRIL, LINC1992, BRI3BPAS1"	TNF- and HNRNPL-related immunoregulatory long noncoding RNA	THRIL	102659353							
chr12	125065366	125143332	12q24.31	12q24.31		614364	"AACS, ACSF1"	Acetoacetyl-CoA synthetase	AACS	65985	ENSG00000081760			Aacs (MGI:1926144)			
chr12	128793193	128823995	12q24.32	12q24.33		615806	"SLC15A4, PHT1, PTR4"	"Solute carrier family 15 (oligopeptide transporter), member 4"	SLC15A4	121260	ENSG00000139370			Slc15a4 (MGI:2140796)			
chr12	129071725	129903666	12q24.3	12q24.33		611257	"TMEM132D, KIAA1944, MOLT"	Transmembrane protein 132D	TMEM132D	121256	ENSG00000151952			Tmem132d (MGI:3044963)			
chr12	130162458	130165739	12q24.33	12q24.33		606147	FZD10	"Frizzled, Drosophila, homolog of, 10"	FZD10	11211	ENSG00000111432			Fzd10 (MGI:2136761)			
chr12	130396132	130716360	12q24.33	12q24.33		611602	"RIMBP2, KIAA0318"	RIMS-binding protein 2	RIMBP2	23504	ENSG00000060709			Rimbp2 (MGI:2443235)			
chr12	130337886	130412707	Chr.12	12q24.33		605571	PIWIL1	"Piwi, Drosophila, homolog of"	PIWIL1	9271	ENSG00000125207			Piwil1 (MGI:1928897)			
chr12	130789599	130839273	12q24.33	12q24.33		132350	"STX2, EPIM, STX2C, STX2B, STX2A"	Epimorphin (syntaxin 2)	STX2	2054	ENSG00000111450			Stx2 (MGI:108059)			
chr12	130871878	130877677	12q24.3	12q24.33		601179	"RAN, ARA24"	Ras-related nuclear protein	RAN	5901	ENSG00000132341			Ran (MGI:1333112)			
chr12	130953906	131141468	12q24.33	12q24.33		613639	"ADGRD1, GPR133, PGR25"	Adhesion G protein-coupled receptor D1	ADGRD1	283383	ENSG00000111452			Adgrd1 (MGI:3041203)			
chr12	131711086	131799737	12q24.33	12q24.33		601945	"SFSWAP, SFRS8, SWAP"	"Splicing factor, suppressor-of-white-apricot family"	SFSWAP	6433	ENSG00000061936			Sfswap (MGI:101760)			
chr12	131828392	131851770	12q24.33	12q24.33		602285	MMP17	Matrix metalloproteinase 17	MMP17	4326	ENSG00000198598			Mmp17 (MGI:1346076)			
chr12	131894733	131923161	12q24.3	12q24.33		603168	"ULK1, UNC51"	UNC51-like kinase 1	ULK1	8408	ENSG00000177169			Ulk1 (MGI:1270126)			
chr12	131929199	131944039	12q24.33	12q24.33		608109	"PUS1, MLASA1"	Pseudourine synthase 1	PUS1	80324	ENSG00000177192		"Myopathy, lactic acidosis, and sideroblastic anemia 1, 600462 (3), Autosomal recessive"	Pus1 (MGI:1929237)			
chr12	131949919	132080465	12q24.33	12q24.33		606265	"EP400, TNRC12, KIAA1498"	p400 SWI2/SNF2-related protein	EP400	57634	ENSG00000183495			Ep400 (MGI:1276124)			
chr12	132144420	132152472	12q24.33	12q24.33		612819	"NOC4L, NOC4"	"Nucleolar complex-associated protein 4, S. cerevisiae, homolog of"	NOC4L	79050	ENSG00000184967			Noc4l (MGI:2140843)			
chr12	132196371	132329318	12q24.33	12q24.33		606251	"GALNT9, GALNACT9"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 9	GALNT9	50614	ENSG00000182870	REc		Galnt9 (MGI:2677965)			
chr12	132471570	132476637	12q24.3	12q24.33		601932	MUC8	"Mucin 8, tracheobronchial"	MUC8	100129528							
chr12	132618779	132623735	12q24.33	12q24.33		600844	"P2RX2, P2X2, DFNA41"	"Purinergic receptor P2X, ligand-gated ion channel, 2"	P2RX2	22953	ENSG00000187848		"Deafness, autosomal dominant 41, 608224 (3), Autosomal dominant"	P2rx2 (MGI:2665170)			
chr12	132623757	132687523	12q24.3	12q24.33		174762	"POLE1, CRCS12, FILS"	"Polymerase (DNA directed), epsilon-1"	POLE	5426	ENSG00000177084		"{Colorectal cancer, susceptibility to, 12}, 615083 (3), Autosomal dominant; FILS syndrome, 615139 (3), Autosomal recessive"	Pole (MGI:1196391)			
chr12	132687605	132704990	12q24.33	12q24.33		617399	PXMP2	Peroxisomal membrane protein 2	PXMP2	5827	ENSG00000176894			Pxmp2 (MGI:107487)			
chr12	132710806	132722736	12q24.33	12q24.33		614939	PGAM5	"Phosphogycerate mutase family, member 5"	PGAM5	192111	ENSG00000247077			Pgam5 (MGI:1919792)			
chr12	132725666	132761887	12q24.33	12q24.33		616062	"ANKLE2, LEM4, KIAA0692, MCPH16"	Ankyrin repeat- and LEM domain-containing protein 2	ANKLE2	23141	ENSG00000176915	mutation identified in 1 MCPH16 family	"?Microcephaly 16, primary, autosomal recessive, 616681 (3), Autosomal recessive"	Ankle2 (MGI:1261856)			
chr12	132768908	132829130	Chr.12	12q24.33		602581	GOLGA3	"Golgi autoantigen, golgin subfamily A, 3"	GOLGA3	2802	ENSG00000090615			Golga3 (MGI:96958)			
chr12	132840351	132887617	12q24.33	12q24.33		605209	CHFR	Checkpoint protein with FHA and ring-finger domains	CHFR	55743	ENSG00000072609			Chfr (MGI:2444898)			
chr12	132986347	133027101	12q24.33	12q24.33		194537	ZNF26	Zinc finger protein-26 (KOX20)	ZNF26	7574	ENSG00000198393						
chr12	133079469	133107673	12q24.32-q24.33	12q24.33		604082	ZNF140	Zinc finger protein-140	ZNF140	7699	ENSG00000196387						
chr12	133130627	133159464	12q13-qter	12q24.33		194538	"ZNF10, KOX1"	Zinc finger protein-10 (KOX 1)	ZNF10	7556	ENSG00000256223	same 300kb fragment as ZNF26					
chr12	133181408	133207111	12q24.3	12q24.33		604753	ZNF268	Zinc finger protein 268	ZNF268	10795	ENSG00000090612						
chr12	0	133275309	Chr.12			191120	TUBAL1	"Tubulin, alpha-like-1"									
chr13	0	27200000	13pter-q12.13			610158	"FECD2, FCD1"	"Corneal dystrophy, Fuchs endothelial, 2"		100188278		max lod at D13S1304	"Corneal dystrophy, Fuchs endothelial, 2, 610158 (2), Autosomal dominant"				
chr13	4600000	10100000	13p12			180450	RNR1	Ribosomal RNA-1	RNR1	6052							
chr13	17700000	114364328	13q			604595	"CLQTL1, CLF"	Cholesterol level quantitative trait locus 1		54501			"[Cholesterol level QTL 1], 604595 (2)"				
chr13	18900000	22600000	13q12.11			612312	ADHD6	"Attention deficit-hyperactivity disorder, susceptibility to, 6"		100190791		max lod at rs1974047	"{Attention deficit-hyperactivity disorder, susceptibility to, 6}, 612312 (2)"				
chr13	18900000	54700000	13q12-q14			605844	ATOD5	"Dermatitis, atopic, 5"		117188		max lod at D13S218	"{Dermatitis, atopic, susceptibility to, 5}, 605844 (2)"				
chr13	18900000	22600000	13q12.11			609384	"CFEOM3C, FEOM4"	"Fibrosis of extraocular muscles, congenital, 3C"					"Fibrosis of extraocular muscles, congenital, 3C, 609384 (2), Autosomal dominant"				
chr13	18900000	31600000	13q12			608557	MCI2	"Myocardial infarction, susceptibility to, 2"		100233226		defined by 4-SNP haplotype HapA	"{Myocardial infarction, susceptibility to, 2}, 608557 (2)"				
chr13	19173769	19181851	13q11	13q12.11		602528	TUBA2	"Tubulin, alpha 2"	TUBA3C	7278	ENSG00000198033						
chr13	19422876	19561573	13q12.11	13q12.11		606791	"TPTE2, TPIP"	Transmembrane phosphoinositide 3-phosphatase and tensin homolog 2	TPTE2	93492	ENSG00000132958			Tpte (MGI:2446460)			
chr13	19633647	19673458	13q12.11	13q12.11		611626	"MPHOSPH8, TWA3"	M-phase phosphoprotein 8	MPHOSPH8	54737	ENSG00000196199			Mphosph8 (MGI:1922589)			
chr13	19674751	19783035	13q12.11	13q12.11		612408	"PSPC1, PSP1"	Paraspeckle component 1	PSPC1	55269	ENSG00000121390			Pspc1 (MGI:1913895)			
chr13	19823481	19863635	13q12.11	13q12.11		616443	"ZMYM5, ZNF237, ZNF198L1"	"Zinc finger, MYM-type 5"	ZMYM5	9205	ENSG00000132950			Zmym5 (MGI:3041170)			
chr13	19957405	20091844	13q12.11	13q12.11		602221	"ZMYM2, ZNF198, RAMP, FIM"	"Zinc finger, MYM-type 2"	ZMYM2	7750	ENSG00000121741			Zmym2 (MGI:1923257)			
chr13	20138251	20161326	13q11	13q12.11		121015	"GJA3, CX46, CZP3, CAE3, CTRCT14"	"Gap junction protein, alpha-3, 46kD (connexin 46)"	GJA3	2700	ENSG00000121743		"Cataract 14, multiple types, 601885 (3), Autosomal dominant"	Gja3 (MGI:95714)			
chr13	20187462	20192974	13q11-q12	13q12.11		121011	"GJB2, CX26, DFNB1A, PPK, DFNA3A, KID, HID"	"Gap junction protein, beta-2, 26kD (connexin 26)"	GJB2	2706	ENSG00000165474		"Bart-Pumphrey syndrome, 149200 (3), Autosomal dominant; Deafness, autosomal dominant 3A, 601544 (3), Autosomal dominant; Deafness, autosomal recessive 1A, 220290 (3), Autosomal recessive; Hystrix-like ichthyosis with deafness, 602540 (3), Autosomal dominant; Keratitis-ichthyosis-deafness syndrome, 148210 (3), Autosomal dominant; Keratoderma, palmoplantar, with deafness, 148350 (3), Autosomal dominant; Vohwinkel syndrome, 124500 (3), Autosomal dominant"	Gjb2 (MGI:95720)			
chr13	20221961	20232394	13q12	13q12.11		604418	"GJB6, CX30, DFNA3B, DFNB1B, ECTD2, HED2"	"Gap junction protein, beta-6 (connexin-30)"	GJB6	10804	ENSG00000121742		"Deafness, autosomal dominant 3B, 612643 (3), Autosomal dominant; Deafness, autosomal recessive 1B, 612645 (3), Autosomal recessive; Deafness, digenic GJB2/GJB6, 220290 (3), Autosomal recessive; Ectodermal dysplasia 2, Clouston type, 129500 (3), Autosomal dominant"	Gjb6 (MGI:107588)			
chr13	20403666	20525872	13q12.11	13q12.11		609877	CRYL1	"Crystallin, lambda-1"	CRYL1	51084	ENSG00000165475			Cryl1 (MGI:1915881)			
chr13	20566445	20691436	13q12.1	13q12.11		600595	"IFT88, D13S1056E, TG737"	"Intraflagellar transport 88, Chlamydomonas, homolog of"	IFT88	8100	ENSG00000032742			Ift88 (MGI:98715)			
chr13	20701104	20723099	13p11	13q12.11		607587	IL17D	Interleukin 17D	IL17D	53342	ENSG00000172458	?associated with Hodgkin lymphoma		Il17d (MGI:2446510)			
chr13	20728930	20773957	13q12.11	13q12.11		617793	"EEF1AKMT1, N6AMT2"	EEF1A lysine methyltransferase 1	EEF1AKMT1	221143	ENSG00000150456			Eef1akmt1 (MGI:1915293)			
chr13	20973035	21061582	13q11-q12	13q12.11		604861	LATS2	"Large tumor suppressor, Drosophila, homolog of, 2"	LATS2	26524	ENSG00000150457			Lats2 (MGI:1354386)			
chr13	21140513	21149084	13q12.11	13q12.11		602949	SAP18	"Sin3-associated polypeptide, 18kD"	SAP18	10284	ENSG00000150459			"Sap18b,Sap18 (MGI:3704317,MGI:1277978)"			
chr13	21176232	21179083	13q12.11	13q12.11		611997	MRP63	Mitochondrial ribosomal protein 63	MRPL57	78988	ENSG00000173141	10 pseudogenes		Mrpl57 (MGI:1915090)			
chr13	21492688	21604215	13q12.11	13q12.11		610632	"MICU2, EFHA1"	Mitochondrial calcium uptake protein 2	MICU2	221154	ENSG00000165487			Micu2 (MGI:1915764)			
chr13	21671075	21704500	13q11-q12	13q12.11		600921	"FGF9, SYNS3"	Fibroblast growth factor-9 (glia-activating factor)	FGF9	2254	ENSG00000102678		"Multiple synostoses syndrome 3, 612961 (3), Autosomal dominant"	Fgf9 (MGI:104723)			
chr13	22600000	24900000	13q12.12			614166	MYP20	"Myopia 20, autosomal dominant"		100682326		associated with rs9318086	"Myopia 20, autosomal dominant, 614166 (2)"				
chr13	23160307	23325164	13q12	13q12.12		608896	"SGCG, LGMD2C, DMDA1, SCG3"	"Sarcoglycan, gamma (35kD dystrophin-associated glycoprotein)"	SGCG	6445	ENSG00000102683		"Muscular dystrophy, limb-girdle, type 2C, 253700 (3), Autosomal recessive"	Sgcg (MGI:1346524)			
chr13	23328822	23433727	13q12	13q12.12		604490	"SACS, ARSACS"	Sacsin	SACS	26278	ENSG00000151835		"Spastic ataxia, Charlevoix-Saguenay type, 270550 (3), Autosomal recessive"				
chr13	23570247	23676104	13q12.11-q12.3	13q12.12		606122	"TAJ, TROY"	Toxicity and JNK inducer	TNFRSF19	55504	ENSG00000127863			Tnfrsf19 (MGI:1352474)			
chr13	23730188	23889447	13q12	13q12.12		602241	"MIPEP, COXPD31"	Mitochondrial intermediate peptidase	MIPEP	4285	ENSG00000027001		"Combined oxidative phosphorylation deficiency 31, 617228 (3), Autosomal recessive"	Mipep (MGI:1917728)			
chr13	23888886	23892103	13q12.12	13q12.12		617122	"C1QTNF9BAS1, PCOTH"	C1QTNF9B antisense RNA 1	PCOTH	542767	ENSG00000205861						
chr13	23891098	23897501	13q12.12	13q12.12		614148	"C1QTNF9B, CTRP9B"	C1q- and tumor necrosis factor-related protein 9B	C1QTNF9B	387911	ENSG00000205863			C1qtnf9 (MGI:3045252)			
chr13	23979625	24307073	13q12.12	13q12.12		613324	"SPATA13, ASEF2"	Spermatogenesis-associated protein 13	SPATA13	221178	ENSG00000182957			Spata13 (MGI:104838)			
chr13	24307165	24322530	13q12.12	13q12.12		614285	"C1QTNF9A, CTRP9, C1QTNF9"	C1q- and tumor necrosis factor-related protein 9A	C1QTNF9	338872	ENSG00000240654						
chr13	24420929	24512992	13q11	13q12.12		607519	"PARP4, ADPRTL1, VPARP, KIAA0177"	Poly(ADP-ribose) polymerase 4	PARP4	143	ENSG00000102699			Parp4 (MGI:2685589)			
chr13	24680410	24711784	13q12.1-q12.3	13q12.12		182360	"ATP12A, ATP1AL1"	"ATPase, H+/K+ transporting, nongastric, alpha polypeptide"	ATP12A	479	ENSG00000075673			Atp12a (MGI:1926943)			
chr13	24747640	24888815	13q12.1	13q12.12		605793	RNF17	RING finger protein-17	RNF17	56163	ENSG00000132972			Rnf17 (MGI:1353419)			
chr13	24882273	24922888	13q12.2	13q12.12-q12.13		609279	"CENPJ, CPAP, MCPH6, SCKL4"	Centromeric protein J	CENPJ	55835	ENSG00000151849	mutation identified in 1 SCKL4 family	"Microcephaly 6, primary, autosomal recessive, 608393 (3), Autosomal recessive; ?Seckel syndrome 4, 613676 (3), Autosomal recessive"	Cenpj (MGI:2684927)			
chr13	25161678	25172450	13q12.13	13q12.13		614659	"FAM123A, AMER2"	"Family with sequence similarity 123, member A (APC membrane recruitment protein 2)"	AMER2	219287	ENSG00000165566			Amer2 (MGI:1919375)			
chr13	25246200	25287565	13q12	13q12.13		603561	MTMR6	Myotubularin-related protein 6	MTMR6	9107	ENSG00000139505			Mtmr6 (MGI:2145637)			
chr13	25301083	25349794	13q12.1	13q12.13		607615	"NUP58, NUPL1, KIAA0410"	Nucleoporin 58kDa	NUP58	9818	ENSG00000139496			Nupl1 (MGI:1919094)			
chr13	25372010	26025850	13q12	13q12.13		605870	"ATP8A2, ATPIB, CAMRQ4"	"ATPase, class I, type 8A, member 2"	ATP8A2	51761	ENSG00000132932		"?Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4, 615268 (3), Autosomal recessive"	Atp8a2 (MGI:1354710)			
chr13	26044596	26051059	13q12.13	13q12.13		617324	"SHISA2, C13orf13, TMEM46"	"Shisa family, member 2"	SHISA2	387914	ENSG00000180730			Shisa2 (MGI:2444716)			
chr13	26132114	26223084	13q12.11	13q12.13		604242	RNF6	RING finger protein-6	RNF6	6049	ENSG00000127870		"Esophageal carcinoma, somatic, 133239 (3)"	Rnf6 (MGI:1921382)			
chr13	26254103	26405237	13q12	13q12.13		603184	CDK8	Cyclin-dependent kinase 8	CDK8	1024	ENSG00000132964			Cdk8 (MGI:1196224)			
chr13	26539138	26688944	13q12	13q12.13		605068	"WASF3, WAVE3, SCAR3"	WAS protein family member 3	WASF3	10810	ENSG00000132970			Wasf3 (MGI:2658986)			
chr13	26755199	26760785	13q12	13q12.13		600752	GPR12	G protein-coupled receptor-12	GPR12	2835	ENSG00000132975			Gpr12 (MGI:101909)			
chr13	27066149	27171895	13q12.13	13q12.13		603091	"USP12, UBH1"	Ubiquitin-specific protease 12	USP12	219333	ENSG00000152484			Usp12 (MGI:1270128)			
chr13	27200000	39500000	13q12.2-q13			157900	"MBS, MBS1"	Moebius syndrome	MBS1	4156			"?Moebius syndrome, 157900 (2), Autosomal dominant, Isolated cases"				
chr13	27251554	27256567	13q12.2	13q12.2		603636	"RPL21, HYPT12"	Ribosomal protein L21	RPL21	6144	ENSG00000122026		"Hypotrichosis 12, 615885 (3), Autosomal dominant"	Rpl21 (MGI:1278340)			
chr13	27270326	27273766	13q12.2	13q12.2		612403	RASL11A	"RAS-like, family 11, member A"	RASL11A	387496	ENSG00000122035			Rasl11a (MGI:1916145)			
chr13	27424543	27435708	13q12.3-q13.1	13q12.2		600860	"GTF3A, TFIIIA"	General transcription factor IIIA	GTF3A	2971	ENSG00000122034			Gtf3a (MGI:1913846)			
chr13	27545912	27621105	13q12.2	13q12.2		609733	"LNX2, PDZRN1"	Ligand of numb protein X2	LNX2	222484	ENSG00000139517			Lnx2 (MGI:2155959)			
chr13	27620742	27667421	13q12.2	13q12.2		613715	"POLR1D, RPA16, RPAC2, TCS2"	"Polymerase I, RNA, subunit D"	POLR1D	51082	ENSG00000186184		"Treacher Collins syndrome 2, 613717 (3), Autosomal recessive, Autosomal dominant"	Polr1d (MGI:108403)			
chr13	27792642	27793951	13q12.2	13q12.2		616542	"GSX1, GSH1"	GS homeobox 1	GSX1	219409	ENSG00000169840			Gsx1 (MGI:95842)			
chr13	27919981	27926313	13q12.1	13q12.2		600733	"PDX1, IPF1, MODY4, PAGEN1"	Pancreas/duodenum homeobox protein 1	PDX1	3651	ENSG00000139515		"{Diabetes mellitus, type II, susceptibility to}, 125853 (3), Autosomal dominant; MODY, type IV, 606392 (3); Pancreatic agenesis 1, 260370 (3), Autosomal recessive"	Pdx1 (MGI:102851)			
chr13	27960917	27969367	13q12.3	13q12.2		600297	"CDX2, CDX3"	Caudal type homeo box transcription factor 2	CDX2	1045	ENSG00000165556			Cdx2 (MGI:88361)			
chr13	27978105	27988636	13q12.2	13q12.2		615804	URAD	Ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase	URAD	646625	ENSG00000183463			Urad (MGI:3647519)			
chr13	28003273	28100591	13q12	13q12.2		136351	FLT3	fms-related tyrosine kinase-3	FLT3	2322	ENSG00000122025		"Leukemia, acute lymphoblastic, somatic, 613065 (3); Leukemia, acute myeloid, reduced survival in, somatic, 601626 (3); Leukemia, acute myeloid, somatic, 601626 (3)"	Flt3 (MGI:95559)			
chr13	28135020	28295337	13q12.2	13q12.2		617448	PAN3	PABP-dependent poly(A) nuclease 3	PAN3	255967	ENSG00000152520			Pan3 (MGI:1919837)			
chr13	28300345	28495127	13q12	13q12.3		165070	FLT1	fms-related tyrosine kinase-1 (vascular endothelial growth factor/vascular permeability factor receptor)	FLT1	2321	ENSG00000102755	150kb from FLT3		Flt1 (MGI:95558)			
chr13	28659003	28678956	13q12.3	13q12.3		613386	"POMP, UMP1"	Proteasome maturation protein	POMP	51371	ENSG00000132963		"Keratosis linearis with ichthyosis congenita and sclerosing keratoderma, 601952 (3), Autosomal recessive"	Pomp (MGI:1913787)			
chr13	28700079	28719012	13q12.3	13q12.3		616764	SLC46A3	"Solute carrier family 46, member 3"	SLC46A3	283537	ENSG00000139508			Slc46a3 (MGI:1918956)			
chr13	29509409	29595687	13q12.3	13q12.3		104615	"SLC7A1, ATRC1"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 1"	SLC7A1	6541	ENSG00000139514	distal to ATP1AL1		Slc7a1 (MGI:88117)			
chr13	29764407	29850682	13q12-q13	13q12.3		604711	UBL3	Ubiquitin-like 3	UBL3	5412	ENSG00000122042			Ubl3 (MGI:1344373)			
chr13	30200025	30307500	13q12.3	13q12.3		614764	KATNAL1	Katanin p60 subunit A-like 1	KATNAL1	84056	ENSG00000102781			Katnal1 (MGI:2387638)			
chr13	30457915	30617596	13q12	13q12.3		163905	"HMGB1, HMG1"	High-mobility group box 1 (high-mobility group (nonhistone chromosomal) protein 1)	HMGB1	3146	ENSG00000189403						
chr13	30617678	30660769	13q12.3	13q12.3		617470	USPL1	Ubiquitin-specific peptidase-like 1	USPL1	10208	ENSG00000132952			Uspl1 (MGI:2442342)			
chr13	30713477	30764427	13q12	13q12.3		603700	"ALOX5AP, FLAP"	Arachidonate 5-lipoxygenase-activating protein	ALOX5AP	241	ENSG00000132965		"{Stroke, susceptibility to}, 601367 (3), Multifactorial"	Alox5ap (MGI:107505)			
chr13	31134973	31162387	13q12.3	13q12.3		610703	"HSPH1, HSP105, KIAA0201"	Heat-shock 105/110kD protein 1	HSPH1	10808	ENSG00000120694			Hsph1 (MGI:105053)			
chr13	31199974	31332275	13q12.3	13q12.3		610308	"B3GLCT, B3GALTL, B3GTL"	Beta 3-glucosyltransferase	B3GLCT	145173	ENSG00000187676		"Peters-plus syndrome, 261540 (3), Autosomal recessive"	B3glct (MGI:2685903)			
chr13	31600000	54700000	13q13-q14.3			600631	ENUR1	"Enuresis, nocturnal, 1"	ENUR1	2031			"Enuresis, nocturnal, 1, 600631 (2), Autosomal dominant"				
chr13	31600000	33400000	13q13.1			612089	HPRHP	Hypophosphatemic rickets and hyperparathyroidism		100188880		?due to altered KLOTHO expression	"Hypophosphatemic rickets and hyperparathyroidism, 612089 (2), Autosomal dominant"				
chr13	31739541	31802871	13q13.1	13q13.1		606655	"LGR8, GREAT"	Leucine-rich repeat-containing G protein-coupled receptor 8	RXFP2	122042	ENSG00000133105			Rxfp2 (MGI:2153463)			
chr13	32031299	32299121	13q13.1	13q13.1		614818	"FRY, C13orf14"	"Furry, Drosophila, homolog of"	FRY	10129	ENSG00000073910			Fry (MGI:2443895)			
chr13	32315479	32399671	13q12.3	13q13.1		600185	"BRCA2, FANCD1, BROVCA2, GLM3, PNCA2"	BRCA2 gene	BRCA2	675	ENSG00000139618		"{Breast cancer, male, susceptibility to}, 114480 (3), Autosomal dominant; {Breast-ovarian cancer, familial, 2}, 612555 (3), Autosomal dominant; Fanconi anemia, complementation group D1, 605724 (3), Autosomal recessive; {Glioblastoma 3}, 613029 (3), Autosomal recessive; {Medulloblastoma}, 155255 (3), Autosomal recessive, Autosomal dominant; {Pancreatic cancer 2}, 613347 (3); {Prostate cancer}, 176807 (3), Autosomal dominant; Wilms tumor, 194070 (3), Autosomal dominant, Somatic mutation"	Brca2 (MGI:109337)			
chr13	32432487	32542709	13q13.1	13q13.1		615788	"N4BP2L2, PFAAP5"	NEDD4-binding protein 2-like 2	N4BP2L2	10443	ENSG00000244754			N4bp2l2 (MGI:2687207)			
chr13	32586426	32778019	13q12.3	13q13.1		605333	AS3	Androgen-induced prostate proliferative shutoff-associated protein	PDS5B	23047	ENSG00000083642			Pds5b (MGI:2140945)			
chr13	33016062	33066144	13q12	13q13.1		604824	"KL, KLOTHO"	Klotho	KL	9365	ENSG00000133116		"{Coronary artery disease, susceptibility to} (3); Tumoral calcinosis, hyperphosphatemic, 211900 (3), Autosomal recessive"	Kl (MGI:1101771)			
chr13	33103134	33676834	13q12.3	13q13.1-q13.2		609866	"STARD13, DLC2"	Start domain-containing protein 13	STARD13	90627	ENSG00000133121			Stard13 (MGI:2385331)			
chr13	33818068	33973945	13q12.3-q13	13q13.2		600405	RFC3	"Replication factor C3, 38kD (activator 1, 38kD)"	RFC3	5983	ENSG00000133119			Rfc3 (MGI:1916513)			
chr13	34900000	39500000	13q13.3			612796	IBD27	Inflammatory bowel disease 27		100302059			"{Inflammatory bowel disease 27}, 612796 (2)"				
chr13	34900000	72800000	13q13.3-q21			263450	PAPA5	"Polydactyly, postaxial, type A5"		101241897		between D13S1288 and D13S632	"Polydactyly, postaxial, type A5, 263450 (2), Autosomal recessive"				
chr13	34942286	35672736	13q13.2	13q13.3		604889	NBEA	Neurobeachin	NBEA	26960	ENSG00000172915	site of FRA13A		Nbea (MGI:1347075)			
chr13	35473788	35476694	13q13	13q13.3		601280	MAB21L1	mab-21 (C. elegans)-like 1	MAB21L1	4081	ENSG00000180660			Mab21l1 (MGI:1333773)			
chr13	35768651	36132019	13q13	13q13.3		604742	"DCLK1, DCAMKL1, CLICK1, CL1, KIAA0369"	Doublecortin-like kinase 1	DCLK1	9201	ENSG00000133083			Dclk1 (MGI:1330861)			
chr13	36168207	36214614	13q13.3	13q13.3		616066	SOHLH2	Spermatogenesis- and oogenesis-specific basic helix-loop-helix protein 2	SOHLH2	54937	ENSG00000120669						
chr13	36301637	36370179	13q12.3	13q13.3		607111	SPG20	Spartin	SPART	23111	ENSG00000133104		"Troyer syndrome, 275900 (3), Autosomal recessive"				
chr13	36430487	36442881	13q12.3-q13	13q13.3		604036	CCNA1	Cyclin A1	CCNA1	8900	ENSG00000133101			Ccna1 (MGI:108042)			
chr13	36819201	36829602	13q14	13q13.3		601861	RFXAP	Regulatory factor X-associated protein	RFXAP	5994	ENSG00000133111		"Bare lymphocyte syndrome, type II, complementation group D, 209920 (3), Autosomal recessive"	Rfxap (MGI:2180854)			
chr13	36844830	36920720	13q12-q14	13q13.3		603295	"MADH9, SMAD9, MADH6, PPH2"	"Mothers against decapentaplegic, Drosophila, homolog of, 9"	SMAD9	4093	ENSG00000120693		"Pulmonary hypertension, primary, 2, 615342 (3), Autosomal dominant"	Smad9 (MGI:1859993)			
chr13	36949769	36999366	13q13.3	13q13.3		604565	ALG5	"Alg5, S. cerevisiae, homolog of"	ALG5	29880	ENSG00000120697			Alg5 (MGI:1913498)			
chr13	37000372	37009613	13q13.1	13q13.3		606019	"EXOSC8, OIP2, RRP43, PCH1C"	Exosome component 8	EXOSC8	11340	ENSG00000120699		"Pontocerebellar hypoplasia, type 1C, 616081 (3), Autosomal recessive"	Exosc8 (MGI:1916889)			
chr13	37009311	37059713	13q13.3	13q13.3		613417	"FAM48A, P38IP, C13orf19"	"Family with sequence similarity 48, member A"	SUPT20H	55578	ENSG00000102710						
chr13	37562581	37598843	13q13.3	13q13.3		608777	"POSTN, OSF2, PN"	Periostin	POSTN	10631	ENSG00000133110			Postn (MGI:1926321)			
chr13	37632062	37870424	13q13.1-q13.2	13q13.3		603651	"TRPC4, TRP4"	"Transient receptor potential cation channel, subfamily C, member 4"	TRPC4	7223	ENSG00000133107			Trpc4 (MGI:109525)			
chr13	38349770	38363006	13q13.3	13q13.3		610553	"UFM1, HLD14"	Ubiquitin-fold modifier 1	UFM1	51569	ENSG00000120686		"Leukodystrophy, hypomyelinating, 14, 617899 (3), Autosomal recessive"	Ufm1 (MGI:1915140)			
chr13	38687035	38887130	13q13.3	13q13.3		608945	"FREM2, FRASRS2"	FRAS1-related extracellular matrix protein 2	FREM2	341640	ENSG00000150893		"Fraser syndrome 2, 617666 (3), Autosomal recessive"	Frem2 (MGI:2444465)			
chr13	38965924	38990858	13q13	13q13.3		608327	"STOML3, SRO"	Stomatin-like protein 3	STOML3	161003	ENSG00000133115			Stoml3 (MGI:2388072)			
chr13	39342891	39603218	13q12	13q13.3-q14.1		606710	LHFP	Lipoma HMGIC fusion partner	LHFPL6	10186	ENSG00000183722			Lhfp (MGI:1920048)			
chr13	39500000	54700000	13q14			606643	BMIQ2	Body mass index quantitative trait locus 2	BMIQ2	192149		max lod at D13S257	"[Body mass index QTL2], 606643 (2)"				
chr13	39500000	54700000	13q14			612110	BMND9	Bone mineral density quantitative trait locus 9		100188882		associated with rs9594759	"[Bone mineral density QTL 9], 612110 (2)"				
chr13	39500000	54700000	13q14			109543	"CLLS2, D13S25, DBM"	"Leukemia, chronic lymphocytic, susceptibility to, 2"		8101		>530kb telomeric to RB1	"{Leukemia, chronic lymphocytic, susceptibility to, 2}, 109543 (2), Autosomal dominant"				
chr13	39500000	54700000	13q14			613884	"DEL13q14, C13DELq14"	Chromosome 13q14 deletion syndrome					"Chromosome 13q14 deletion syndrome, 613884 (4), Autosomal dominant, Isolated cases"				
chr13	39500000	54700000	13q14			109350	GER	Gastroesophageal reflux		59330			"Gastroesophageal reflux, 109350 (2), Autosomal dominant"				
chr13	39500000	44600000	13q14.11			613407	LPRS6	"Leprosy, susceptibility to, 6"		100499166		associated with rs9533634 and rs3764147	"{Leprosy, susceptibility to, 6}, 613407 (2)"				
chr13	39500000	54700000	13q14			601499	"RIEG2, RGS2"	"Rieger syndrome, type 2"	RIEG2	6012			"Rieger syndrome, type 2, 601499 (2), Autosomal dominant"				
chr13	39500000	54700000	13q14			607584	SPG24	"Spastic paraplegia 24, autosomal recessive"	SPG24	338090			"Spastic paraplegia 24, autosomal recessive, 607584 (2), Autosomal recessive"				
chr13	39500000	54700000	13q14			194370	XRS	X-ray sensitivity		8102							
chr13	39655626	39791664	13q13.3	13q14.11		606977	"COG6, COD2, KIAA1134, CDG2L, SHNS"	Component of oligomeric golgi complex 6	COG6	57511	ENSG00000133103		"Congenital disorder of glycosylation, type IIl, 614576 (3), Autosomal recessive; Shaheen syndrome, 615328 (3), Autosomal recessive"	Cog6 (MGI:1914792)			
chr13	40555663	40666596	13q14.1	13q14.11		136533	"FOXO1A, FKHR"	Forkhead box O1A (forkhead in rhabdomyosarcoma)	FOXO1	2308	ENSG00000150907	chimeric with PAX3 in t(2;13); fuses with PAX3	"Rhabdomyosarcoma, alveolar, 268220 (3), Autosomal recessive"	Foxo1 (MGI:1890077)			
chr13	40729295	40771210	13q13.3	13q14.11		611992	MRPS31	Mitochondrial ribosomal protein S31	MRPS31	10240	ENSG00000102738	4 pseudogenes		Mrps31 (MGI:1913153)			
chr13	40789410	40812459	13q14	13q14.11		603861	"SLC25A15, ORNT1, HHH"	"Solute carrier family 25 (mitochondrial carrier), member 15 (ornithine transporter 1)"	SLC25A15	10166	ENSG00000102743	with deficiency of factors VII and X in 3 unrelated cases	"Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3), Autosomal recessive"	Slc25a15 (MGI:1342274)			
chr13	40931918	41061383	13q14.11	13q14.11		189973	"ELF1, RIA1, EFTUD1"	E74-like factor 1	ELF1	1997	ENSG00000120690			Elf1 (MGI:107180)			
chr13	41061256	41084011	13q14.11	13q14.11		604981	"WBP4, FBP21"	WW domain-containing binding protein 4	WBP4	11193	ENSG00000120688			Wbp4 (MGI:109568)			
chr13	41127572	41132799	13q14.11	13q14.11		617738	KBTBD6	Kelch repeat- and BTB domain-containing protein 6	KBTBD6	89890	ENSG00000165572			Kbtbd6 (MGI:3643058)			
chr13	41189833	41194583	13q14.11	13q14.11		617739	KBTBD7	Kelch repeat- and BTB domain-containing protein 7	KBTBD7	84078	ENSG00000120696			Kbtbd7 (MGI:2685141)			
chr13	41216368	41312037	13q14.1-q14.3	13q14.11		604601	MTRF1	"Translational release factor, mitochondrial, 1"	MTRF1	9617	ENSG00000120662			Mtrf1 (MGI:2384815)			
chr13	41457405	41470876	13q12-q14	13q14.11		610077	RGC32	Response gene to complement 32	RGCC	28984	ENSG00000102760			Rgcc (MGI:1913464)			
chr13	41566824	41961745	13q14.11	13q14.11		617509	"VWA8, KIAA0564"	von Willebrand factor A domain-containing protein 8	VWA8	23078	ENSG00000102763			Vwa8 (MGI:1919008)			
chr13	42040035	42256583	13q14.11	13q14.11		604071	DGKH	"Diacylglycerol kinase, eta, 130kD"	DGKH	160851	ENSG00000102780			Dgkh (MGI:2444188)			
chr13	42271469	42323266	13q14.11	13q14.11		604696	"AKAP11, AKAP220"	A-kinase anchor protein 11	AKAP11	11215	ENSG00000023516			Akap11 (MGI:2684060)			
chr13	42562735	42608012	13q14	13q14.11		602642	"TNFSF11, OPGL, TRANCE, OPTB2"	"Tumor necrosis factor ligand superfamily, member 11 (osteoprotegerin ligand)"	TNFSF11	8600	ENSG00000120659		"Osteopetrosis, autosomal recessive 2, 259710 (3), Autosomal recessive"	Tnfsf11 (MGI:1100089)			
chr13	42886387	42992311	13q13.3	13q14.11		607441	EPSTI1	Epithelial stromal interaction 1	EPSTI1	94240	ENSG00000133106			Epsti1 (MGI:1915168)			
chr13	43023225	43109169	13q14.1	13q14.11		615339	"DNAJC15, MCJ"	"DNAJ/HSP40 homolog, subfamily C, member 15"	DNAJC15	29103	ENSG00000120675			Dnajc15 (MGI:1913398)			
chr13	43213132	43786979	13q14.11	13q14.11		610914	"ENOX1, CNOX"	ECTO-NOX disulfide-thiol exchanger 1	ENOX1	55068	ENSG00000120658			Enox1 (MGI:2444896)			
chr13	43821958	43880022	13q14.11	13q14.11		613408	CCDC122	Coiled-coil domain-containing protein 122	CCDC122	160857	ENSG00000151773			Ccdc122 (MGI:1918358)			
chr13	43879177	43893931	13q14.11	13q14.11		613409	"LACC1, C13orf31"	Laccase (multicopper reductase) domain-containing protein 1	LACC1	144811	ENSG00000179630			Lacc1 (MGI:2445077)			
chr13	44432142	44576824	13q14	13q14.11		607715	"TSC22D1, TSC22"	"TSC22 domain family, member 1"	TSC22D1	8848	ENSG00000102804			Tsc22d1 (MGI:109127)			
chr13	44939248	44989482	13q14	13q14.12		604354	"NUFIP1, NUFIP"	Nuclear fragile X mental retardation protein-interacting protein 1	NUFIP1	26747	ENSG00000083635	pseudogene on 6q12		Nufip1 (MGI:1351474)			
chr13	45119829	45284104	13q14.12-q14.13	13q14.12-q14.13		189969	"GTF2F2, TF2F2, RAP30"	"General transcription factor IIF, polypeptide 2, 30kD"	GTF2F2	2963	ENSG00000188342			Gtf2f2 (MGI:1915955)			
chr13	45333470	45341283	13q12-q14	13q14.13		600763	"TPT1, HRF"	"Tumor protein, translationally-controlled 1"	TPT1	7178	ENSG00000133112			Tpt1 (MGI:104890)			
chr13	45393315	45434015	13q14.11	13q14.13		610793	"SLC25A30, KMCP1"	"Solute carrier family 25 (mitochondrial carrier, kidney), member 30"	SLC25A30	253512	ENSG00000174032			Slc25a30 (MGI:1914804)			
chr13	45464894	45536697	13q14.12	13q14.13		606975	"COG3, SEC34"	Component of oligomeric golgi complex 3	COG3	83548	ENSG00000136152			Cog3 (MGI:2450151)			
chr13	45780269	45851710	13q14.12	13q14.13		615609	SIAH3	"SIAH E3 ubiquitin protein ligase family, member 3"	SIAH3	283514	ENSG00000215475			Siah3 (MGI:2685758)			
chr13	45954464	46052793	13q14.13	13q14.13		616453	"ZC3H13, KIAA0853"	Zinc finger CCCH domain-containing protein 13	ZC3H13	23091	ENSG00000123200						
chr13	46053065	46105075	13q14.11	13q14.13		603101	"CPB2, CPU, TAFI"	"Carboxypeptidase B2, plasma (carboxypeptidase U)"	CPB2	1361	ENSG00000080618			Cpb2 (MGI:1891837)			
chr13	46125922	46182323	13q14.1-q14.3	13q14.13		153430	LCP1	Lymphocyte cytosolic protein-1 (plasmin)	LCP1	3936	ENSG00000136167			Lcp1 (MGI:104808)			
chr13	46553160	46753040	13q14	13q14.1-q14.2		610368	"LRCH1, KIAA1016"	Leucine-rich repeats and calponin homology domain-containing 1	LRCH1	23143	ENSG00000136141			Lrch1 (MGI:2443390)			
chr13	46700000	46700000	13q14.2-q14.1			608049	AUTS3	"Autism, susceptibility to, 3"		387577			"{Autism susceptibility 3}, 608049 (2), Isolated cases, Multifactorial"				
chr13	46771255	46797699	13q14.11	13q14.2		133280	ESD	Esterase D; S-formylglutathione hydrolase	ESD	2098	ENSG00000139684	"proximal to RB1, WND"		"Esd,Esd-ps (MGI:3781082,MGI:95421)"			
chr13	46831541	46897075	13q14-q21	13q14.2		182135	HTR2A	5-hydroxytryptamine (serotonin) receptor-2A	HTR2A	3356	ENSG00000102468		"{Alcohol dependence, susceptibility to}, 103780 (3), Multifactorial; {Anorexia nervosa, susceptibility to}, 606788 (3); {Major depressive disorder, response to citalopram therapy in}, 608516 (3); {Obsessive-compulsive disorder, susceptibility to}, 164230 (3), Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant; {Seasonal affective disorder, susceptibility to}, 608516 (3)"	Htr2a (MGI:109521)			
chr13	47942655	48001325	13q14.2	13q14.2		603921	"SUCLA2, MTDPS5"	"Succinate-CoA ligase, ADP-forming, beta subunit"	SUCLA2	8803	ENSG00000136143		"Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria), 612073 (3), Autosomal recessive"	Sucla2 (MGI:1306775)			
chr13	48037566	48052741	13q14.2	13q14.2		615792	"NUDT15, MTH2, NUDT15D"	Nucleoside diphosphate-linked moiety X motif 15	NUDT15	55270	ENSG00000136159		"{Thiopurines, poor metabolism of, 2}, 616903 (3), Autosomal dominant"	Nudt15 (MGI:2443366)			
chr13	48075727	48095140	13q14.2	13q14.2		605718	"MED4, DRIP36, HSPC126"	"Mediator of RNA polymerase II transcription, subunit 4, S. cerevisiae, homolog of"	MED4	29079	ENSG00000136146			Med4 (MGI:1914631)			
chr13	48233137	48262095	13q14	13q14.2		603904	"ITM2B, BRI, ABRI, FBD, RDGCA"	Integral membrane protein 2B (BRI gene)	ITM2B	9445	ENSG00000136156	mutation identified in 1 RDGCA family	"Dementia, familial British, 176500 (3), Autosomal dominant; Dementia, familial Danish, 117300 (3), Autosomal dominant; ?Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities, 616079 (3), Autosomal dominant"	Itm2b (MGI:1309517)			
chr13	48303746	48481889	13q14.1-q14.2	13q14.2		614041	RB1	Retinoblastoma-1	RB1	5925	ENSG00000139687		"Bladder cancer, somatic, 109800 (3); Osteosarcoma, somatic, 259500 (3); Retinoblastoma, 180200 (3), Autosomal dominant, Somatic mutation; Retinoblastoma, trilateral, 180200 (3), Autosomal dominant, Somatic mutation; Small cell cancer of the lung, somatic, 182280 (3)"	Rb1 (MGI:97874)			
chr13	48400896	48444703	13q14.12-q14.2	13q14.2		609239	"LPAR6, P2RY5, P2Y5, LAH3, ARWH1, HYPT8"	Lysophosphatidic acid receptor 6	LPAR6	10161	ENSG00000139679	in intron 17 of RB gene	"Hypotrichosis 8, 278150 (3), Autosomal recessive; Woolly hair, autosomal recessive 1, with or without hypotrichosis, 278150 (3), Autosomal recessive"	Lpar6 (MGI:1914418)			
chr13	48488962	48535996	13q14.3	13q14.2		603524	"RCBTB2, CHC1L"	RCC1 domain- and BTB domain-containing protein 2	RCBTB2	1102	ENSG00000136161			Rcbtb2 (MGI:1917200)			
chr13	48653710	48711225	13q14	13q14.2		605666	"CYSLTR2, CYSLT2"	Cysteinyl leukotriene receptor 2	CYSLTR2	57105	ENSG00000152207			Cysltr2 (MGI:1917336)			
chr13	48975240	49209778	13q14.2	13q14.2		615794	"FNDC3A, KIAA0970, HUGO"	Fibronectin type III domain-containing protein 3A	FNDC3A	22862	ENSG00000102531			Fndc3a (MGI:1196463)			
chr13	49220337	49222376	13q14-q21	13q14.2		602885	"MLNR, GPR38"	Motilin receptor	MLNR	2862	ENSG00000102539						
chr13	49308649	49444850	13q14.2	13q14.2		612175	CAB39L	Calcium-binding protein 39-like protein	CAB39L	81617	ENSG00000102547			Cab39l (MGI:1914081)			
chr13	49444292	49495002	13q14	13q14.2		607865	"SETDB2, CLLD8"	"SET domain protein, bifurcated, 2"	SETDB2	83852	ENSG00000136169			Setdb2 (MGI:2685139)			
chr13	49495609	49528991	13q14.1	13q14.2		607796	"PHF11, NYREN34"	PHD finger protein 11	PHF11	51131	ENSG00000136147			"Phf11b,Phf11c,Phf11d,Phf11a (MGI:3645789,MGI:1277133,MGI:1918441,MGI:3648476)"			
chr13	49531943	49585586	13q14	13q14.2		607867	"RCBTB1, CLLD7, GLP, RDEOA"	RCC1 domain- and BTB domain-containing protein 1	RCBTB1	55213	ENSG00000136144		"Retinal dystrophy with or without extraocular anomalies, 617175 (3), Autosomal recessive"	Rcbtb1 (MGI:1918580)			
chr13	49628298	49633871	13q14.3	13q14.2		609351	"ARL11, ARLTS1"	ADP-ribosylation factor-like 11	ARL11	115761	ENSG00000152213			Arl11 (MGI:2444054)			
chr13	49660675	49691486	13q14.2	13q14.2		617335	EBPL	Emopamil-binding protein-like	EBPL	84650	ENSG00000123179			Ebpl (MGI:1915427)			
chr13	49699306	49792920	13q14.3	13q14.2		601892	KPNA3	Karyopherin (importin) alpha-3	KPNA3	3839	ENSG00000102753			Kpna3 (MGI:1100863)			
chr13	49912701	49936500	13q14	13q14.2		607866	"CLLD6, C13orf1"	Chronic lymphocytic leukemia deletion region gene 6	SPRYD7	57213	ENSG00000123178			Spryd7 (MGI:1913924)			
chr13	49982548	50125540	13q14	13q14.2		605766	"DLEU2, LEU2, BCMSUN"	Deleted in lymphocytic leukemia 2	DLEU2	8847							
chr13	49997006	50018466	13q14.3	13q14.2		605661	"TRIM13, RFP2, LEU5"	Tripartite motif-containing protein 13	TRIM13	10206	ENSG00000204977			Trim13 (MGI:1913847)			
chr13	50015253	50020921	13q14.3	13q14.2		607947	"KCNRG, DLTET"	Potassium channel regulator	KCNRG	283518	ENSG00000198553			Kcnrg (MGI:2685591)			
chr13	50048972	50049060	13q14.3	13q14.2		609704	"MIR16-1, MIRN16-1"	Micro RNA 16-1	MIR16-1	406950							
chr13	50049118	50049200	13q14.3	13q14.2		609703	"MIR15A, MIRN15A"	Micro RNA 15A	MIR15A	406948							
chr13	50082168	50528642	13q14	13q14.2-q14.3		605765	"DLEU1, LEU1"	Deleted in lymphocytic leukemia 1	DLEU1	10301							
chr13	50300000	54700000	13q14.3			612894	STQTL20	Stature quantitative trait locus 20		100302685		associated with rs3118914	"{Stature QTL 20}, 612894 (2)"				
chr13	50909677	50970461	13q14.1	13q14.3		610326	"RNASEH2B, DLEU8, FLJ11712, AGS2"	"Ribonuclease H2, subunit B"	RNASEH2B	79621	ENSG00000136104		"Aicardi-Goutieres syndrome 2, 610181 (3), Autosomal recessive"	Rnaseh2b (MGI:1914403)			
chr13	50994510	51066156	13q14.3	13q14.3		603695	GUCY1B2	"Guanylate cyclase 1, soluble, beta-2"	GUCY1B2	2974							
chr13	51353170	51453332	13q14.3	13q14.3		604331	"INTS6, DDX26, DICE1"	Integrator complex subunit 6	INTS6	26512	ENSG00000102786			Ints6 (MGI:1202397)			
chr13	51584193	51766798	13q14.3	13q14.3		610418	WDFY2	WD repeat- and FYVE domain-containing protein 2	WDFY2	115825	ENSG00000139668			Wdfy2 (MGI:2442811)			
chr13	51767992	51804161	13q14.3	13q14.3		616163	"DHRS12, SDR40C1"	"Short-chain dehydrogenase reductase family, member 12"	DHRS12	79758	ENSG00000102796						
chr13	51907819	51910752	13q14-q21	13q14.3		608857	CTAGE3	Cutaneous T-cell lymphoma-associated antigen 3	CTAGE3P	220112							
chr13	51932668	52012129	13q14.3-q21.1	13q14.3		606882	"ATP7B, WND"	"ATPase, Cu++ transporting, beta polypeptide"	ATP7B	540	ENSG00000123191		"Wilson disease, 277900 (3), Autosomal recessive"	Atp7b (MGI:103297)			
chr13	52012386	52029647	13q14.3	13q14.3		613666	"ALG11, KIAA1266, CDG1P"	"Alg11, S. cerevisiae, homolog of"	ALG11	440138	ENSG00000253710		"Congenital disorder of glycosylation, type Ip, 613661 (3), Autosomal recessive"	Alg11 (MGI:2142632)			
chr13	52064761	52129091	13q14.3	13q14.3		616731	NEK5	Never in mitosis gene A-related kinase 5	NEK5	341676	ENSG00000197168			Nek5 (MGI:2142824)			
chr13	52132642	52159860	13q14.2	13q14.3		604044	NEK3	Never in mitosis gene A-related kinase 3	NEK3	4752	ENSG00000136098			Nek3 (MGI:1344371)			
chr13	52377166	52406493	13q14.3	13q14.3		616821	"THSD1, TMTSP"	Thrombospondin type 1 domain-containing protein 1	THSD1	55901	ENSG00000136114			Thsd1 (MGI:1929096)			
chr13	52412601	52450677	13q14.3	13q14.3		610903	"VPS36, EAP45"	"Vacuolar protein sorting 36, S. cerevisiae, homolog of"	VPS36	51028	ENSG00000136100			Vps36 (MGI:1917410)			
chr13	52455359	52476630	13q14	13q14.3		611569	"CKAP2, TMAP, LB1"	Cytoskeleton-associated protein 2	CKAP2	26586	ENSG00000136108			Ckap2 (MGI:1931797)			
chr13	52652690	52700755	13q14.3	13q14.3		604098	"SUGT1, SGT1"	"Suppressor of G2 allele of Skp1, S. Cerevisiae, homolog of"	SUGT1	10910	ENSG00000165416			Sugt1 (MGI:1915205)			
chr13	52703263	52739811	13q14-q21	13q14.3		605147	"LECT1, CHM1"	Leukocyte cell derived chemotaxin 1 (chondromodulin)	CNMD	11061	ENSG00000136110			Cnmd (MGI:1341171)			
chr13	52843973	52848639	13q14.3	13q14.3		603580	PCDH8	Protocadherin 8	PCDH8	5100	ENSG00000136099			Pcdh8 (MGI:1306800)			
chr13	53028740	53052060	13q14.3	13q14.3		614061	"OLFM4, GC1, GW112"	Olfactomedin 4	OLFM4	10562	ENSG00000102837			Olfm4 (MGI:2685142)			
chr13	54700000	72800000	13q21			613289	ATXN8	Ataxin 8	ATXN8	724066		CAG repeat results in polyglutamine expansion protein	"Spinocerebellar ataxia 8, 608768 (3), Autosomal dominant"				
chr13	54700000	101100000	13q21-q32			602085	PAPA2	"Postaxial polydactyly, type A2"		8103			"Postaxial polydactyly, type A2, 602085 (2), Autosomal dominant"				
chr13	54700000	72800000	13q21			607134	SLI3	"Specific language impairment QTL, 3"		780906		max with D13S1317	"Specific language impairment QTL, 3, 607134 (2)"				
chr13	57630103	57728930	13q21.1	13q21.1		611760	"PCDH17, PCDH68"	Protocadherin 17	PCDH17	27253	ENSG00000118946			Pcdh17 (MGI:2684924)			
chr13	59665582	60163984	13q21.2	13q21.2		614567	"DIAPH3, DIA2, DRF3, AUNA1, NSDAN"	"Diaphanous, Drosophila, homolog of, 3"	DIAPH3	81624	ENSG00000139734		"Auditory neuropathy, autosomal dominant, 1, 609129 (3), Autosomal dominant"	Diaph3 (MGI:1927222)			
chr13	60396456	60573878	13q21.2	13q21.2		614392	TDRD3	Tudor domain-containing protein 3	TDRD3	81550	ENSG00000083544			Tdrd3 (MGI:2444023)			
chr13	61409684	61415521	13q21.2	13q21.2		614449	"PCDH20, PCDH13"	Protocadherin 20	PCDH20	64881	ENSG00000280165			Pcdh20 (MGI:2443376)			
chr13	66302833	67230335	13q21.1	13q21.32		603581	PCDH9	Protocadherin 9	PCDH9	5101	ENSG00000184226			Pcdh9 (MGI:1306801)			
chr13	69700592	70108492	13q21	13q21.33		605332	KLHL1	Kelch-like 1	KLHL1	57626	ENSG00000150361			Klhl1 (MGI:2136335)			
chr13	70107212	70139752	13q21	13q21.33		603680	"ATXN8OS, SCA8, KLHL1AS"	Ataxin 8 opposite strand	ATXN8OS	6315		due to CTG repeat in untranslated DNA	"Spinocerebellar ataxia 8, 608768 (3), Autosomal dominant"				
chr13	71437965	71868067	13q22	13q21.33		603803	DACH	"Dachshund, Drosophila, homolog of"	DACH1	1602	ENSG00000276644			Dach1 (MGI:1277991)			
chr13	72708356	72727799	13q21.33-q22.1	13q21.33		613448	"C13orf37, MOZART1"	Mitotic spindle-organizing protein associated with a ring of gamma-tubulin	MZT1	440145	ENSG00000204899			Mzt1 (MGI:1924039)			
chr13	72727738	72756197	13q22.1	13q21.33		610510	"BORA, C13orf34"	Aurora borealis	BORA	79866	ENSG00000136122			Bora (MGI:1924994)			
chr13	72755401	72782127	13q21-q22	13q21.33		607533	"DIS3, KIAA1008"	"Dis3, S. pombe, homolog of"	DIS3	22894	ENSG00000083520			Dis3 (MGI:1919912)			
chr13	72782022	73016453	13q21-q22	13q21.3-q22.1		607532	"PIBF1, JBTS33"	Progesterone-induced blocking factor 1	PIBF1	10464	ENSG00000083535		"Joubert syndrome 33, 617767 (3), Autosomal recessive"	Pibf1 (MGI:1261910)			
chr13	72800000	78500000	13q22			142700	DDH1	Developmental dysplasia of the hip 1		780896			"Developmental dysplasia of the hip 1, 142700 (2), Multifactorial"				
chr13	72800000	101100000	13q22-q32			167870	PAND1	Panic disorder syndrome 1		387572			"Panic disorder syndrome 1, 167870 (2), ?Autosomal dominant"				
chr13	73686011	74168294	13q22	13q22.1		607531	"KLF12, AP2REP"	Kruppel-like factor 12	KLF12	11278	ENSG00000118922			Klf12 (MGI:1333796)			
chr13	75284663	75483143	13q22.2	13q22.2		612465	"TBC1D4, AS160, KIAA0603, NIDDM5"	"TPC1 domain family, member 4"	TBC1D4	9882	ENSG00000136111		"{Diabetes mellitus, noninsulin-dependent, 5}, 616087 (3)"	Tbc1d4 (MGI:2429660)			
chr13	75525213	75549438	13q22	13q22.2		612377	COMMD6	COMM domain-containing protein 6	COMMD6	170622	ENSG00000188243						
chr13	75549479	75606019	13q22	13q22.2		603090	UCHL3	Ubiquitin carboxyl-terminal esterase L3	UCHL3	7347	ENSG00000118939			Uchl3 (MGI:1355274)			
chr13	75620433	75859869	13q21-q22	13q22.2		604362	"LMO7, FBXO20, FBX20, KIAA0858"	LIM domain only 7	LMO7	4008	ENSG00000136153			Lmo7 (MGI:1353586)			
chr13	76880168	76886404	13q21	13q22.3		610521	"KCTD12, PFET1, KIAA1778, C13orf2"	Potassium channel tetramerization domain-containing protein 12	KCTD12	115207	ENSG00000178695			Kctd12 (MGI:2145823)			
chr13	76928450	76929089	13q22	13q22.3		602543	"TNFRSF11B, OPG, OCIF"	"Tumor necrosis factor receptor superfamily, member 11B"	BTF3P11	690							
chr13	76948558	76958641	13q22.3	13q22.3		615275	"ACOD1, IRG1"	Aconitate decarboxylase 1	ACOD1	730249	ENSG00000102794			Acod1 (MGI:103206)			
chr13	76991923	77002516	13q22.3	13q22.3		608102	CLN5	CLN5 gene	CLN5	1203	ENSG00000102805		"Ceroid lipofuscinosis, neuronal, 5, 256731 (3), Autosomal recessive"	Cln5 (MGI:2442253)			
chr13	76992596	77027195	13q22	13q22.3		605653	"FBXL3A, FBL3A, FBL3"	F-box and leucine-rich repeat protein 3A	FBXL3	26224	ENSG00000005812			Fbxl3 (MGI:1354702)			
chr13	77044656	77327097	13q22	13q22.3		610392	"MYCBP2, PAM, KIAA0916"	Myc-binding protein 2	MYCBP2	23077	ENSG00000005810			Mycbp2 (MGI:2179432)			
chr13	77535673	77645262	13q22	13q22.3		604112	SCEL	Sciellin	SCEL	8796	ENSG00000136155			Scel (MGI:1891228)			
chr13	77697673	77764241	13q22.3	13q22.3		610491	SLAIN1	"SLAIN motif family, member 1"	SLAIN1	122060	ENSG00000139737			Slain1 (MGI:2145578)			
chr13	77895480	77975722	13q22	13q22.3		131244	"EDNRB, HSCR2, ABCDS, WS4A"	Endothelin receptor type B	EDNRB	1910	ENSG00000136160	?piebald lethal in mouse	"ABCD syndrome, 600501 (3), Autosomal recessive; {Hirschsprung disease, susceptibility to, 2}, 600155 (3), Autosomal dominant; Waardenburg syndrome, type 4A, 277580 (3), Autosomal recessive, Autosomal dominant"	Ednrb (MGI:102720)			
chr13	78500000	109600000	13q31-q33			193003	NYS4	"Nystagmus 4, congenital, autosomal dominant"	NYS4	317685			"Nystagmus 4, congenital, autosomal dominant, 193003 (2), Autosomal dominant"				
chr13	78599091	78603559	13q21.1-q22	13q31.1		601632	"POU4F1, BRN3A"	"POU domain, class 4, transcription factor 1"	POU4F1	5457	ENSG00000152192			Pou4f1 (MGI:102525)			
chr13	78614285	78659178	13q31.1	13q31.1		615906	"RNF219, C13orf7"	Ring finger protein 219	RNF219	79596	ENSG00000152193			Rnf219 (MGI:1919736)			
chr13	79480721	79556076	13q22.2	13q31.1		610041	"NDFIP2, N4WBP5A, KIAA1165"	NEDD4 family-interacting protein 2	NDFIP2	54602	ENSG00000102471			Ndfip2 (MGI:1923523)			
chr13	80011076	80026662	13q31.1	13q31.1		615230	LNCR13Q1	Long noncoding RNA on 13q (TCONS_00021856)	LINC01080	101515984							
chr13	80335975	80341114	13q31.1	13q31.1		602466	"SPRY2, IGAN3"	"Sprouty, Drosophila, homolog of, 2"	SPRY2	10253	ENSG00000136158	mutation identified in 1 IGAN3 family	"{?IgA nephropathy, susceptibility to, 3}, 616818 (3), Autosomal dominant"	Spry2 (MGI:1345138)			
chr13	83877204	83882392	13q31	13q31.1		609678	"SLITRK1, KIAA1910, TTM"	"SLIT- and NTRK-like family, member 1"	SLITRK1	114798	ENSG00000178235	mutation identified in 1 TTM patient	"Tourette syndrome, 137580 (3), Autosomal dominant; ?Trichotillomania, 613229 (3), Autosomal dominant, Multifactorial"	Slitrk1 (MGI:2679446)			
chr13	85792786	85799347	13q31	13q31.1		609681	"SLITRK6, DFNMYP"	"SLIT- and NTRK-like family, member 6"	SLITRK6	84189	ENSG00000184564		"Deafness and myopia, 221200 (3), Autosomal recessive"	Slitrk6 (MGI:2443198)			
chr13	87671231	87679618	13q31	13q31.2		609680	"SLITRK5, KIAA0918"	"SLIT- and NTRK-like family, member 5"	SLITRK5	26050	ENSG00000165300			Slitrk5 (MGI:2679448)			
chr13	89400000	97500000	13q31.3-q32.1			610840	MMVP3	"Mitral valve prolapse, myxomatous 3"		100034705		max lod at D13S132	"Mitral valve prolapse, myxomatous 3, 610840 (2), Autosomal dominant"				
chr13	89400000	94400000	13q31.3			609572	PPR2	Photoparoxysmal response 2		780910		max lod at D13S1230	"Photoparoxysmal response 2, 609572 (2)"				
chr13	91347819	91354574	13q31.3	13q31.3		609415	"MIR17HG, MIRH1, MIHG1, MIRHG1, C13orf25, FGLDS2"	Micro RNA 17 host gene	MIR17HG	407975			"Feingold syndrome 2, 614326 (3), Autosomal dominant"				
chr13	91350604	91350687	13q31.3	13q31.3		609416	"MIR17, MIR91, MIRN17"	Micro RNA 17	MIR17	406952		within C13orf25; sequence encodes 2 micro RNAs					
chr13	91350750	91350820	13q31.3	13q31.3		609417	"MIR18A, MIRN18A"	Micro RNA 18A	MIR18A	406953		within C13orf25					
chr13	91350890	91350971	13q31.3	13q31.3		609418	"MIR19A, MIRN19A"	Micro RNA 19A	MIR19A	406979		within C13orf25					
chr13	91351064	91351134	13q31.3	13q31.3		609420	"MIR20A, MIRN20A"	Micro RNA 20A	MIR20A	406982		within C13orf25					
chr13	91351191	91351277	13q31.3	13q31.3		609419	"MIR19B1, MIRN19B1"	Micro RNA 19B1	MIR19B1	406980		within C13orf25					
chr13	91351313	91351390	13q31.3	13q31.3		609422	"MIR92A1, MIR92-1, MIRN92-1"	Micro RNA 92A1	MIR92A1	407048		within C13orf25					
chr13	91398618	92867236	13q32	13q31.3		602446	GPC5	Glypican 5	GPC5	2262	ENSG00000179399			Gpc5 (MGI:1194894)			
chr13	93226807	94408019	13q32	13q31.3-q32.1		604404	"GPC6, OMIMD1"	Glypican 6	GPC6	10082	ENSG00000183098		"Omodysplasia 1, 258315 (3), Autosomal recessive"	Gpc6 (MGI:1346322)			
chr13	94400000	101100000	13q32			614629	KTCN7	Keratoconus 7		100887822		max lod at D13S159	"Keratoconus 7, 614629 (2), Autosomal dominant"				
chr13	94400000	101100000	13q32			156600	"MCOR, C13DELq32, DEL13q32"	"Microcoria, congenital (chromosome 13q32 deletion syndrome)"				35-80kb deletion encompassing TGDS and GPR180	"Microcoria, congenital, 156600 (4), Autosomal dominant"				
chr13	94400000	101100000	13q32			603176	SCZD7	"Schizophrenia susceptibility locus, chromosome 13q-related"	SCZD7	8401			"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr13	94400000	101100000	13q32			609903	SLEB5	"Systemic lupus erythematosus, susceptibility to, 5"		100188798		max lod at D13S892	"{Systemic lupus erythematosus, susceptibility to, 5}, 609903 (2)"				
chr13	94400000	109600000	13q32-q33			606258	STQTL4	Stature quantitative trait locus 4		282550		max lod at D13S779 and D13S797	"{Stature QTL 4}, 606258 (2)"				
chr13	94437303	94549412	13q31-q32	13q32.1		191275	"DCT, TYRP2"	Dopachrome tautomerase (dopachrome delta-isomerase; tyrosinase-related protein 2)	DCT	1638	ENSG00000080166			Dct (MGI:102563)			
chr13	94574053	94596274	13q32.1	13q32.1		616146	"TGDS, SDR2E1, CATMANS"	"TDP-glucose 4,6-dehydratase"	TGDS	23483	ENSG00000088451		"Catel-Manzke syndrome, 616145 (3), Autosomal recessive"	Tgds (MGI:1923605)			
chr13	94601849	94634644	13q31	13q32.1		607787	"GPR180, ITR"	G protein-coupled receptor 180	GPR180	160897	ENSG00000152749			Gpr180 (MGI:1930949)			
chr13	94709621	94712542	13q31-q32	13q32.1		604974	SOX21	SRY-box 21	SOX21	11166	ENSG00000125285			Sox21 (MGI:2654070)			
chr13	95019828	95301445	13q32	13q32.1		605250	"ABCC4, MRP4, MOATB"	"ATP-binding cassette, subfamily C, member 4"	ABCC4	10257	ENSG00000125257			Abcc4 (MGI:2443111)			
chr13	95433587	95579755	13q32.1	13q32.1		617579	"CLDN10, OSPL, CPETRL3, HELIX"	Claudin 10	CLDN10	9071	ENSG00000134873		"HELIX syndrome, 617671 (3), Autosomal recessive"	Cldn10 (MGI:1913101)			
chr13	95578201	95644705	13q31	13q32.1		608671	"DZIP1, KIAA0996"	DAZ-interacting zinc finger protein 1	DZIP1	22873	ENSG00000134874			Dzip1 (MGI:1914311)			
chr13	95677138	95794988	13q32	13q32.1		601184	"DNAJC3, PRKRI, P58, ACPHD"	"DnaJ, E. coli, homolog of, subfamily C, member 3 (protein kinase inhibitor p58)"	DNAJC3	5611	ENSG00000102580	mutation identified in 1 ACPHD family	"?Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, 616192 (3), Autosomal recessive"	Dnajc3 (MGI:107373)			
chr13	95801579	96053481	13q32.1	13q32.1		605898	"UGGT2, HUGT2"	UDP-glucose glycoprotein glucosyltransferase 2	UGGT2	55757	ENSG00000102595			Uggt2 (MGI:1913685)			
chr13	96090633	96839561	13q32-q33	13q32.1		609401	HS6ST3	Heparan sulfate 6-O-sulfotransferase 3	HS6ST3	266722	ENSG00000185352			Hs6st3 (MGI:1354960)			
chr13	96985718	96994729	13q32.1	13q32.1		606922	GPR80	G protein-coupled receptor 80	OXGR1	27199	ENSG00000165621			Oxgr1 (MGI:2685145)			
chr13	97434220	97467997	13q34	13q32.1		179540	RAP2A	"RAP2, member of RAS oncogene family (K-rev)"	RAP2A	5911	ENSG00000125249			Rap2a (MGI:97855)			
chr13	97953640	98024295	13q32.2	13q32.2		602008	"IPO5, RANBP5, KPNB3"	Importin 5	IPO5	3843	ENSG00000065150			Ipo5 (MGI:1917822)			
chr13	98142561	98449772	13q32.2	13q32.2		602654	"FARP1, CDEP"	"FERM, ARHGEF, and pleckstrin domain-containing protein 1"	FARP1	10160	ENSG00000152767			Farp1 (MGI:2446173)			
chr13	98450198	98577150	13q31.2-q32.3	13q32.2		604984	"STK24, MST3, MST3B"	Serine/threonine protein kinase 24	STK24	8428	ENSG00000102572			Stk24 (MGI:2385007)			
chr13	98683800	98752674	13q33-q34	13q32.2-q32.3		600544	"SLC15A1, HPECT1"	"Solute carrier family 15 (oligopeptide transporter), member 1"	SLC15A1	6564	ENSG00000088386			Slc15a1 (MGI:1861376)			
chr13	98793486	99086405	13q32.3	13q32.3		607325	"ZIZ1, KIAA1058"	Zizimin 1	DOCK9	23348	ENSG00000088387			Dock9 (MGI:106321)			
chr13	99254712	99262497	13q32	13q32.3		602042	GPR18	G protein-coupled receptor-18	GPR18	2841	ENSG00000125245			Gpr18 (MGI:107859)			
chr13	99294272	99307494	13q32.3	13q32.3		605741	"GPR183, EBI2"	G protein-coupled receptor 183	GPR183	1880	ENSG00000169508			Gpr183 (MGI:2442034)			
chr13	99501373	99564047	13q32.3	13q32.3		604678	TM9SF2	"Transmembrane 9 superfamily, member 2"	TM9SF2	9375	ENSG00000125304			Tm9sf2 (MGI:1915309)			
chr13	99606663	99909458	13q32	13q32.3		609686	"CLYBL, CLB"	Citrate lyase beta-like	CLYBL	171425	ENSG00000125246			Clybl (MGI:1916884)			
chr13	99962963	99971908	13q32.3	13q32.3		617896	"ZIC5, OPR"	"Zic family, member 5"	ZIC5	85416	ENSG00000139800			Zic5 (MGI:1929518)			
chr13	99981755	99986772	13q32	13q32.3		603073	"ZIC2, HPE5"	"ZIC family, member 2"	ZIC2	7546	ENSG00000043355		"Holoprosencephaly 5, 609637 (3), Autosomal dominant"	Zic2 (MGI:106679)			
chr13	100089014	100530436	13q32	13q32.3		232000	PCCA	"Propionyl Coenzyme A carboxylase, alpha polypeptide"	PCCA	5095	ENSG00000175198		"Propionicacidemia, 606054 (3), Autosomal recessive"	Pcca (MGI:97499)			
chr13	100530163	100588791	13q32.3	13q32.3		613378	"A2LD1, GGACT"	AIG1-like domain-containing protein 1	GGACT	87769	ENSG00000134864			Ggact (MGI:2385008)			
chr13	101053773	101417205	13q33.11	13q32.3-q33.1		611549	"NALCN, IHPRF1, CLIFAHDD"	"Sodium leak channel, nonselective"	NALCN	259232	ENSG00000102452		"Congenital contractures of the limbs and face, hypotonia, and developmental delay, 616266 (3), Autosomal dominant; Hypotonia, infantile, with psychomotor retardation and characteristic facies 1, 615419 (3), Autosomal recessive"	Nalcn (MGI:2444306)			
chr13	101100000	114364328	13q33.1-q34			610361	OFC9	Orofacial cleft 9		100462724		associated with rs1830756	"Orofacial cleft 9, 610361 (2)"				
chr13	101452592	101720856	13q33	13q33.1		604234	"ITGBL1, TIED"	"Integrin, beta-like 1"	ITGBL1	9358	ENSG00000198542			Itgbl1 (MGI:2443439)			
chr13	101720854	102402427	13q34	13q33.1		601515	"FGF14, FHF4, SCA27"	Fibroblast growth factor-14	FGF14	2259	ENSG00000102466		"Spinocerebellar ataxia 27, 609307 (3), Autosomal dominant"	Fgf14 (MGI:109189)			
chr13	102596935	102679957	13q32-q33	13q33.1		190470	TPP2	Tripeptidyl peptidase II	TPP2	7174	ENSG00000134900			Tpp2 (MGI:102724)			
chr13	102678781	102704310	13q33.1	13q33.1		615259	"METTL21C, C13orf39"	Methyltransferase-like 21C	METTL21C	196541	ENSG00000139780			Mettl21c (MGI:3611450)			
chr13	102784280	102799053	13q33	13q33.1		611613	"KDELC1, EP58"	KDEL motif-containing 1	KDELC1	79070	ENSG00000134901			Kdelc1 (MGI:1919300)			
chr13	102845840	102876000	13q33	13q33.1		133530	"ERCC5, XPG, COFS3"	"Excision-repair, complementing defective, in Chinese hamster, number 5"	ERCC5	2073	ENSG00000134899		"Cerebrooculofacioskeletal syndrome 3, 616570 (3), Autosomal recessive; Xeroderma pigmentosum, group G, 278780 (3), Autosomal recessive; Xeroderma pigmentosum, group G/Cockayne syndrome, 278780 (3), Autosomal recessive"	Ercc5 (MGI:103582)			
chr13	103043997	103066845	13q33	13q33.1		601295	"SLC10A2, NTCP2, PBAM"	"Solute carrier family 10 (sodium/bile acid cotransporter family), member 2"	SLC10A2	6555	ENSG00000125255		"Bile acid malabsorption, primary, 613291 (3), Autosomal recessive"	Slc10a2 (MGI:1201406)			
chr13	104200000	106400000	13q33.2			614318	VUR5	Vesicoureteral reflux 5		100820760		nearest marker rs4476030	"Vesicoureteral reflux 5, 614318 (2)"				
chr13	105459054	105505680	13q34	13q33.2		607415	"DAOAAS, G30"	DAOA antisense RAN	DAOA-AS1	282706							
chr13	105465866	105491033	13q34	13q33.2		607408	"DAOA, G72"	D-amino acid oxidase activator	DAOA	267012	ENSG00000182346		"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr13	106489730	106535039	13q33	13q33.3		600527	"EFNB2, EPLG5, LERK5, HTKL"	eph-related receptor tyrosine kinase ligand 5 (ephrin-B2)	EFNB2	1948	ENSG00000125266			Efnb2 (MGI:105097)			
chr13	106543313	106568165	13q33.3	13q33.3		614046	ARGLU1	Arginine- and glutamate-rich protein 1	ARGLU1	55082	ENSG00000134884			Arglu1 (MGI:2442985)			
chr13	108207441	108218367	13q22-q34	13q33.3		601837	"LIG4, LIG4S"	"Ligase IV, DNA, ATP-dependent"	LIG4	3981	ENSG00000174405		"LIG4 syndrome, 606593 (3), Autosomal recessive; {Multiple myeloma, resistance to}, 254500 (3), Somatic mutation"	Lig4 (MGI:1335098)			
chr13	108268239	108308483	13q32-q34	13q33.3		603969	"TNFSF13B, BLYS, BAFF"	"Tumor necrosis factor ligand superfamily, member 13B"	TNFSF13B	10673	ENSG00000102524			Tnfsf13b (MGI:1344376)			
chr13	108495728	109208006	13q33.3	13q33.3		615479	"MYO16, MYAP3, KIAA0865"	Myosin XVI	MYO16	23026	ENSG00000041515			Myo16 (MGI:2685951)			
chr13	109600000	114364328	13q34			614211	DFNA33	"Deafness, autosomal dominant 33"	DFNA33	29779		maximum lod at D13S285	"Deafness, autosomal dominant 33, 614211 (2), Autosomal dominant"				
chr13	109753836	109786566	13q34	13q34		600797	IRS2	Insulin receptor substrate 2	IRS2	8660	ENSG00000185950		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant"	Irs2 (MGI:109334)			
chr13	110148957	110307156	13q34	13q34		120130	"COL4A1, POREN1, HANAC, ICH, BSVD, RATOR"	"Collagen IV, alpha-1 polypeptide"	COL4A1	1282	ENSG00000187498	mutation identified in 1 RATOR family	"Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, 611773 (3), Autosomal dominant; Brain small vessel disease with or without ocular anomalies, 607595 (3), Autosomal dominant; {Hemorrhage, intracerebral, susceptibility to}, 614519 (3); Porencephaly 1, 175780 (3), Autosomal dominant; ?Retinal arteries, tortuosity of, 180000 (3), Autosomal dominant; Schizencephaly, 269160 (3)"	Col4a1 (MGI:88454)			
chr13	110307266	110513208	13q34	13q34		120090	"COL4A2, POREN2, ICH"	"Collagen IV, alpha-2 polypeptide"	COL4A2	1284	ENSG00000134871		"{Hemorrhage, intracerebral, susceptibility to}, 614519 (3); Porencephaly 2, 614483 (3), Autosomal dominant"	Col4a2 (MGI:88455)			
chr13	110615459	110639995	13q34	13q34		615910	CARKD	Carbohydrate kinase domain-containing protein	NAXD	55739	ENSG00000213995			Naxd (MGI:1913353)			
chr13	110641409	110713600	13q34	13q34		612800	"CARS2, COXPD27"	Cysteinyl-tRNA synthetase 2	CARS2	79587	ENSG00000134905		"Combined oxidative phosphorylation deficiency 27, 616672 (3), Autosomal recessive"	Cars2 (MGI:1919191)			
chr13	110712622	110721073	13q34	13q34		601566	ING1	Inhibitor of growth 1	ING1	3621	ENSG00000153487		"Squamous cell carcinoma, head and neck, somatic, 275355 (3)"	Ing1 (MGI:1349481)			
chr13	111114618	111305733	13q34	13q34		605477	"ARHGEF7, PIXB, COOL1"	"Rho guanine nucleotide exchange factor 7 (PAK-interacting exchange factor, beta)"	ARHGEF7	8874	ENSG00000102606			Arhgef7 (MGI:1860493)			
chr13	112067598	112071705	13q34	13q34		602148	SOX1	SRY (sex determining region Y)-box 1	SOX1	6656	ENSG00000182968			Sox1 (MGI:98357)			
chr13	112485004	112606468	13q34	13q34		617818	"TUBGCP3, GCP3, GRIP104, SPC98, ALP6"	Tubulin-gamma complex-associated protein 3	TUBGCP3	10426	ENSG00000126216			Tubgcp3 (MGI:2183752)			
chr13	112690033	112887167	13q34	13q34		605868	"ATP11A, ATPIS, ATPIH"	"ATPase, class VI, type 11A"	ATP11A	23250	ENSG00000068650			Atp11a (MGI:1354735)			
chr13	112894377	113099738	13q34	13q34		609499	"MCF2L, OST, KIAA0362"	MCF2-like protein	MCF2L	23263	ENSG00000126217			Mcf2l (MGI:103263)			
chr13	113105772	113120680	13q34	13q34		613878	F7	Coagulation factor VII	F7	2155	ENSG00000057593		"Factor VII deficiency, 227500 (3), Autosomal recessive; {Myocardial infarction, decreased susceptibility to}, 608446 (3)"	F7 (MGI:109325)			
chr13	113122798	113149528	13q34	13q34		613872	F10	Coagulation factor X	F10	2159	ENSG00000126218		"Factor X deficiency, 227600 (3), Autosomal recessive"	F10 (MGI:103107)			
chr13	113155863	113172385	13q34	13q34		176895	"PROZ, PZ"	Protein Z	PROZ	8858	ENSG00000126231		"[Protein Z deficiency], 614024 (3)"	Proz (MGI:1860488)			
chr13	113165001	113209466	13q34	13q34		613713	PCID2	PCI domain-containing protein 2	PCID2	55795	ENSG00000126226			Pcid2 (MGI:2443003)			
chr13	113208192	113267107	13q34	13q34		603137	CUL4A	Cullin 4A	CUL4A	8451	ENSG00000139842			Cul4a (MGI:1914487)			
chr13	113297153	113323425	13q34	13q34		153330	LAMP1	Lysosome-associated membrane protein-1	LAMP1	3916	ENSG00000185896			Lamp1 (MGI:96745)			
chr13	113421939	113453523	13q31	13q34		610620	"ADPRHL1, ARH2"	ADP-ribosylhydrolase-like 1	ADPRHL1	113622	ENSG00000153531			Adprhl1 (MGI:2442168)			
chr13	113490737	113550228	13q34	13q34		617134	"TMCO3, C13orf11"	Transmembrane and coiled-coil domains protein 3	TMCO3	55002	ENSG00000150403			Tmco3 (MGI:2444946)			
chr13	113584687	113641472	13q34	13q34		189902	"TFDP1, DP1, DRTF1"	Transcription factor Dp-1	TFDP1	7027	ENSG00000198176	pseudogene on 1q32.3		Tfdp1 (MGI:101934)			
chr13	113645770	113735663	13q34	13q34		180381	"GRK1, RHOK, RK"	G protein-dependent receptor kinase 1 (rhodopsin kinase)	GRK1	6011	ENSG00000185974		"Oguchi disease-2, 613411 (3)"	Grk1 (MGI:1345146)			
chr13	113648803	113658197	13q34	13q34		137217	ATP4B	"ATPase, H+, K+ transporting, beta"	ATP4B	496	ENSG00000186009			Atp4b (MGI:88114)			
chr13	113820548	113864102	13q34	13q34		600441	"GAS6, AXLLG, AXSF"	Growth arrest-specific 6	GAS6	2621	ENSG00000183087			Gas6 (MGI:95660)			
chr13	113977782	114132622	13q34	13q34		605182	RASA3	Ras p21 protein activator 3	RASA3	22821	ENSG00000185989			Rasa3 (MGI:1197013)			
chr13	114234844	114272722	13q34	13q34		603461	"CDC16, APC6"	"Cell division cycle 16, S. cerevisiae, homolog of"	CDC16	8881	ENSG00000130177			Cdc16 (MGI:1917207)			
chr13	114281583	114305816	13q34	13q34		605530	"UPF3A, RENT3A"	"UPF3 regulator of nonsense transcripts, yeast, homolog of, A"	UPF3A	65110	ENSG00000169062			Upf3a (MGI:1914281)			
chr13	114314334	114327327	13q34	13q34		616327	"CHAMP1, ZNF828, C13orf8, KIAA1802, MRD40"	Chromosome alignment-maintaining phosphoprotein 1	CHAMP1	283489	ENSG00000198824		"Mental retardation, autosomal dominant 40, 616579 (3), Autosomal dominant"	Champ1 (MGI:1196398)			
chr14	3600000	8000000	14p12			180451	RNR2	Ribosomal RNA-2	RNR2	6053							
chr14	8000000	37400000	14p11.2-q13			606771	"ADIPQTL3, CAQ14"	"Adiponectin, serum level of, quantitative trait locus 3"		171512		between D14S608 and D14S599	"{Adiponectin, serum level of, QTL3}, 606771 (2)"				
chr14	17200000	57600000	14q11-q22			613457	"DEL14q11q22, C14DELq11q22"	Chromosome 14q11-q22 deletion syndrome				contiguous gene syndrome	"Chromosome 14q11-q22 deletion syndrome, 613457 (4), Isolated cases"				
chr14	17200000	32900000	14q11-q12			606675	IBD4	Inflammatory bowel disease 4	IBD4	50608			"{Inflammatory bowel disease 4}, 606675 (2)"				
chr14	17200000	24100000	14q11			617833	ZFHX2AS1	ZFHX2 antisense RNA 1	ZFHX2-AS1	109729160							
chr14	18200000	32900000	14q11.2-q12			609965	DFNA53	"Deafness, autosomal dominant 53"	DFNA53	353347		max lod at D14S1280	"Deafness, autosomal dominant 53, 609965 (2), Autosomal dominant"				
chr14	18200000	37400000	14q11.2-q13			144110	HHPP	Hyperhidrosis palmaris et plantaris		100861529		between D14S283 and D14S264	"Hyperhidrosis palmaris et plantaris, 144110 (2), Autosomal dominant"				
chr14	18200000	32900000	14q11.2-q12			611095	"MRT9, MRT26"	"Mental retardation, autosomal recessive, 9/26"	MRT9	100101424		between rs1998463 and rs243286	"Mental retardation, autosomal recessive, 9/26, 611095 (2), Autosomal recessive"				
chr14	18200000	24100000	14q11.2			612851	NRCLP5	Narcolepsy 5		100302514		"associated with rs1154155, rs12587781, rs1263646"	"{Narcolepsy 5}, 612851 (2)"				
chr14	18200000	32900000	14q11.2-q12			610420	PAURT1	"Preauricular tag, isolated, autosomal dominant, 1"		101669760		between D14S990 and D14S264	"Preauricular tag, isolated, autosomal dominant, 1, 610420 (2), Autosomal dominant"				
chr14	18200000	24100000	14q11.2			605463	RSCIS	"Radiation sensitivity/chromosome instability syndrome, autosomal dominant"		64239			"Radiation sensitivity/chromosome instability syndrome, autosomal dominant (1)"				
chr14	18200000	32900000	14q11.2-q12			610234	SPD3	Synpolydactyly 3		780922		max lod at D14S264	"Synpolydactyly 3, 610234 (2)"				
chr14	18200000	24100000	14q11.2			615443	TRAJ@	T-cell receptor alpha chain joining gene cluster									
chr14	18200000	24100000	14q11.2			615442	TRAV@	T-cell receptor alpha chain variable gene cluster									
chr14	18200000	24100000	14q11.2			615460	TRDD@	T-cell receptor delta chain diversity gene cluster									
chr14	18200000	24100000	14q11.2			615461	TRDJ@	T-cell receptor delta chain joining gene cluster									
chr14	18200000	24100000	14q11.2			615459	TRDV@	T-cell receptor delta chain variable gene cluster									
chr14	20311367	20333311	14q11.1	14q11.2		608249	"C14orf18, HEI10"	Human enhancer of invasion 10	CCNB1IP1	57820	ENSG00000100814			Ccnb1ip1 (MGI:2685134)			
chr14	20343040	20357903	14q11.2	14q11.2		607725	"PARP2, ADPRTL2, ADPRT2"	Poly(ADP-ribose) polymerase 2	PARP2	10038	ENSG00000129484			Parp2 (MGI:1341112)			
chr14	20343070	20343410	14q11.2	14q11.2		608513	"RPPH1, H1RNA"	"Ribonuclease P, RNA component H1"	RPPH1	85495							
chr14	20365666	20413539	14q11.2	14q11.2		601686	"TEP1, TP1"	Telomerase-associated protein-1	TEP1	7011	ENSG00000129566			Tep1 (MGI:109573)			
chr14	20447047	20455107	14q11.2-q12	14q11.2		610107	"OSGEP, FLJ20411, GAMOS3"	O-sialoglycoprotein endopeptidase	OSGEP	55644	ENSG00000092094		"Galloway-Mowat syndrome 3, 617729 (3), Autosomal recessive"	Osgep (MGI:1913496)			
chr14	20455130	20457771	14q12	14q11.2		107748	"APEX, APE"	APEX nuclease (multifunctional DNA repair enzyme)	APEX1	328	ENSG00000100823			Apex1 (MGI:88042)			
chr14	20469378	20478005	14q13.1	14q11.2		164050	"PNP, NP"	Purine nucleoside phosphorylase	PNP	4860	ENSG00000198805	centromeric to TCRA	"Immunodeficiency due to purine nucleoside phosphorylase deficiency, 613179 (3), Autosomal recessive"	"Pnp,Pnp2 (MGI:3712328,MGI:97365)"			
chr14	20556092	20560930	14q11.2	14q11.2		614014	RNAE9	"Ribonuclease A family, 9"	RNASE9	390443	ENSG00000188655			Rnase9 (MGI:3057273)			
chr14	20609335	20609406	14q11	14q11.2		189930	"TRNAP1, TRP1"	tRNA proline-1	TRP-AGG2-5	7217							
chr14	20610131	20610212	14q11-q12	14q11.2		189932	"TRL-AAG2-1, TRNAL1, TRL1"	tRNA leucine (AAG) 2-1	TRL-AAG2-3	7207							
chr14	20613400	20613471	14q11-q12	14q11.2		189931	"TRNAP2, TRP2"	tRNA proline-2	TRP-AGG2-6	7218							
chr14	20613789	20613861	14q11-q12	14q11.2		189933	"TRNAT2, TRT2"	tRNA threonine-2	TRT-TGT3-1	7237							
chr14	20684176	20694185	14q11.2	14q11.2		105850	"ANG, RNASE5, ALS9"	Angiogenin	ANG	283	ENSG00000214274	proximal to TCRA/TCRD	"Amyotrophic lateral sclerosis 9, 611895 (3)"	Ang (MGI:88022)			
chr14	20684212	20700601	14q11.2	14q11.2		601030	"RNASE4, RNS4"	"Ribonuclease, RNase A family, 4"	RNASE4	6038	ENSG00000258818			Rnase4 (MGI:1926217)			
chr14	20722390	20748379	14q11.2	14q11.2		611580	"FAM12A, HE3A"	"Family with sequence similarity 12, member A"	EDDM3A	10876	ENSG00000181562						
chr14	20768426	20770947	14q11.2	14q11.2		611582	"FAM12B, HE3B"	"Family with sequence similarity 12, member B"	EDDM3B	64184	ENSG00000181552			Eddm3b (MGI:2684921)			
chr14	20780955	20782466	14q11.2	14q11.2		601981	RNASE6	"Ribonuclease, RNase A family, k6"	RNASE6	6039	ENSG00000169413			Rnase6 (MGI:1925666)			
chr14	20801355	20802876	14q11.2	14q11.2		180440	"RNASE1, RNS1"	"Ribonuclease, RNase A family, 1 (pancreatic)"	RNASE1	6035	ENSG00000129538			Rnase1 (MGI:97919)			
chr14	20891402	20892347	14q11.2	14q11.2		131398	"RNASE3, RNS3, ECP"	"Ribonuclease, RNase A family, 3 (eosinophil cationic protein)"	RNASE3	6037	ENSG00000169397						
chr14	20955470	20956434	14q11.2	14q11.2		131410	"RNASE2, RNS2, EDN"	"Ribonuclease, RNase A family, 2, liver (eosinophil-derived neurotoxin)"	RNASE2	6036	ENSG00000169385			"Rnase2a,Rnase2b (MGI:1890465,MGI:1858598)"			
chr14	20989805	20997034	14q11.2	14q11.2		616091	"METTL17, METT11D1"	Methyltransferase-like 17	METTL17	64745	ENSG00000165792			Mettl17 (MGI:1098577)			
chr14	20999254	21001874	14q11.2	14q11.2		612166	"SLC39A2, ZIP2"	"Solute carrier family 39 (zinc transporter), member 2"	SLC39A2	29986	ENSG00000165794			Slc39a2 (MGI:2684326)			
chr14	21016762	21070871	14q11.2	14q11.2		605272	NDRG2	N-myc downstream-regulated gene 2	NDRG2	57447	ENSG00000165795			Ndrg2 (MGI:1352498)			
chr14	21024261	21036351	14q11.2	14q11.2		616956	"TPPP2, p18"	"Tubulin polymerization-promoting protein family, member 2"	TPPP2	122664	ENSG00000179636			Tppp2 (MGI:2684923)			
chr14	21042225	21044232	14q11.2	14q11.2		612484	RNASE7	Ribonuclease A family 7	RNASE7	84659	ENSG00000165799						
chr14	21057821	21058454	14q11.2	14q11.2		612485	RNASE8	"Ribonuclease A family, 8"	RNASE8	122665	ENSG00000173431						
chr14	21061275	21090247	14q11.2	14q11.2		610018	"SOLO, FLJ10357"	SOLO gene	ARHGEF40	55701	ENSG00000165801			Arhgef40 (MGI:2685515)			
chr14	21090045	21104720	14q11	14q11.2		605036	ZNF219	Zinc finger protein-219	ZNF219	51222	ENSG00000165804			Zfp219 (MGI:1917140)			
chr14	21209135	21269478	14q11.2	14q11.2		164020	"HNRNPC, HNRPC"	Heterogeneous nuclear ribonucleoprotein C	HNRNPC	3183	ENSG00000092199			Hnrnpc (MGI:107795)			
chr14	21287976	21351315	14q11	14q11.2		605446	"RPGRIP1, LCA6, CORD13"	Retinitis pigmentosa GTPase regulator-interacting protein	RPGRIP1	57096	ENSG00000092200		"Cone-rod dystrophy 13, 608194 (3); Leber congenital amaurosis 6, 613826 (3)"	Rpgrip1 (MGI:1932134)			
chr14	21351471	21384265	14q11.2	14q11.2		605012	"SUPT16H, SPT16"	"Suppressor of ty 16, S. cerevisiae, homolog of"	SUPT16H	11198	ENSG00000092201			Supt16 (MGI:1890948)			
chr14	21385193	21437297	14q11.2	14q11.2		610528	"CHD8, DUPLIN, KIAA1564, AUTS18"	Chromodomain helicase DNA-binding protein 8	CHD8	57680	ENSG00000100888		"{Autism, susceptibility to, 18}, 615032 (3), Autosomal dominant"	Chd8 (MGI:1915022)			
chr14	21459019	21476972	14q11.1-q11.2	14q11.2		607466	RAB2B	Ras-associated protein RAB2B	RAB2B	84932	ENSG00000129472			Rab2b (MGI:1923588)			
chr14	21477175	21499176	14q11.2	14q11.2		614032	"TOX4, LCP1, KIAA0737"	TOX high mobility group box family member 4	TOX4	9878	ENSG00000092203			Tox4 (MGI:1915389)			
chr14	21498130	21511374	14q11.1	14q11.2		612472	"METTL3, IME4"	Methyltransferase-like 3	METTL3	56339	ENSG00000165819			Mettl3 (MGI:1927165)			
chr14	21521079	21537215	14q11.1-q12	14q11.2		602219	"SALL2, HSAL2, COLB"	Sal-like 2	SALL2	6297	ENSG00000165821	mutation identified in 1 COLB family	"?Coloboma, ocular, autosomal recessive, 216820 (3), Autosomal recessive"	Sall2 (MGI:1354373)			
chr14	22462931	22466576	14q11.2	14q11.2		186810	TRDC	T-cell receptor delta chain constant region	TRDC	28526		in midst of TCRA					
chr14	22547505	22552131	14q11.2	14q11.2		186880	"TRAC, TRCA, TRA, IMD7"	T-cell receptor alpha	TRAC	28755		cen--V-C--ter	"Immunodeficiency 7, TCR-alpha/beta deficient, 615387 (3), Autosomal recessive"				
chr14	22564906	22589236	14q11-q12	14q11.2		600243	DAD1	Defender against cell death 1	DAD1	1603	ENSG00000129562			Dad1 (MGI:101912)			
chr14	22766521	22771788	14q11.2	14q11.2		601066	OXA1L	Oxidase (cytochrome c) assembly 1-like	OXA1L	5018	ENSG00000155463			Oxa1l (MGI:1916339)			
chr14	22773221	22819810	14q11.2	14q11.2		603593	"SLC7A7, LPI"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 7"	SLC7A7	9056	ENSG00000155465		"Lysinuric protein intolerance, 222700 (3), Autosomal recessive"	Slc7a7 (MGI:1337120)			
chr14	22829861	22835036	14q11.2	14q11.2		611856	MRPL52	Mitochondrial ribosomal protein L52	MRPL52	122704	ENSG00000172590			Mrpl52 (MGI:1916086)			
chr14	22836532	22847599	14q11-q12	14q11.2		600754	"MMP14, WNCHRS"	Matrix metalloproteinase 14 (membrane-inserted)	MMP14	4323	ENSG00000157227	mutation identified in 1 family	"?Winchester syndrome, 277950 (3)"	Mmp14 (MGI:101900)			
chr14	22871612	22881712	14q11.2	14q11.2		609921	"LRP10, LRP9"	Low density lipoprotein receptor-related protein 10	LRP10	26020	ENSG00000197324			Lrp10 (MGI:1929480)			
chr14	22883164	22887679	14q11.2	14q11.2		616955	REM2	RRAD- and GEM-like GTPase 2	REM2	161253	ENSG00000139890			Rem2 (MGI:2155260)			
chr14	22946227	22957141	14q11.2	14q11.2		613431	"HAUS4, C14orf94"	"HAUS augmin-like complex, subunit 4"	HAUS4	54930	ENSG00000092036			Haus4 (MGI:1261794)			
chr14	23016542	23035219	14q11.2	14q11.2		600306	"PSMB5, LMPX"	"Proteasome subunit, beta type, 5"	PSMB5	5693	ENSG00000100804			Psmb5 (MGI:1194513)			
chr14	23042166	23044059	14q11.2	14q11.2		611137	PSMB11	"Proteasome subunit, beta-type, 11"	PSMB11	122706	ENSG00000222028			Psmb11 (MGI:1921152)			
chr14	23058563	23095613	14q11.2	14q11.2		604562	"ACIN1, KIAA0670"	Acinus	ACIN1	22985	ENSG00000100813			Acin1 (MGI:1891824)			
chr14	23117305	23119610	14q11.2	14q11.2		600749	"CEBPE, CRP1"	"CCAAT/enhancer-binding protein (C/EBP), epsilon"	CEBPE	1053	ENSG00000092067		"Specific granule deficiency, 245480 (3), Autosomal recessive"	Cebpe (MGI:103572)			
chr14	23125294	23183659	14q11.2	14q11.2		604235	"SLC7A8, LAT2"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 8"	SLC7A8	23428	ENSG00000092068			Slc7a8 (MGI:1355323)			
chr14	23273634	23286099	11q11.2	14q11.2		608119	"HOMEZ, KIAA1443"	Homeodomain leucine zipper-containing factor	HOMEZ	57594	ENSG00000215271			Homez (MGI:2678023)			
chr14	23306761	23311758	14q11.2-q12	14q11.2		601931	"BCL2L2, BCLW"	BCL2-like 2	BCL2L2	599	ENSG00000129473			Bcl2l2 (MGI:108052)			
chr14	23320187	23326184	14q11.2-q13	14q11.2		602279	"PABPN1, PABP2, PAB2"	"Poly(A)-binding protein, nuclear 1"	PABPN1	8106	ENSG00000100836		"Oculopharyngeal muscular dystrophy, 164300 (3), Autosomal dominant"	Pabpn1 (MGI:1859158)			
chr14	23346303	23354990	14q11.2	14q11.2		611461	"SLC22A17, NGALR, BOIT, BOCT, NGALR2, NGALR3"	"Solute carrier family 22, organic cation transporter, member 17"	SLC22A17	51310	ENSG00000092096			Slc22a17 (MGI:1926225)			
chr14	23356399	23365632	14q11.2-q12	14q11.2		609906	EFS	Embryonal FYN-associated substrate	EFS	10278	ENSG00000100842			Efs (MGI:105311)			
chr14	23372808	23376402	14q11.2	14q11.2		605658	"IL25, IL17E"	Interleukin 25	IL25	64806	ENSG00000166090			Il25 (MGI:2155888)			
chr14	23376431	23379771	14q11.2	14q11.2		607888	"CMTM5, CKLFSF5"	CKLF-like marvel transmembrane domain-containing 5	CMTM5	116173	ENSG00000166091			Cmtm5 (MGI:2447164)			
chr14	23381989	23408276	14q12	14q11.2		160710	"MYH6, ASD3, MYHCA, CMD1EE, CMH14, SSS3"	"Myosin, heavy polypeptide-6, cardiac muscle, alpha"	MYH6	4624	ENSG00000197616		"Atrial septal defect 3, 614089 (3); Cardiomyopathy, dilated, 1EE, 613252 (3); Cardiomyopathy, hypertrophic, 14, 613251 (3), Autosomal dominant; {Sick sinus syndrome 3}, 614090 (3)"	Myh6 (MGI:97255)			
chr14	23388595	23388665	14q12	14q11.2		611116	"MIR208A, MIRN208A, MIR208, MIRN208"	Micro RNA 208A	MIR208A	406990							
chr14	23412737	23435685	14q12	14q11.2		160760	"MYH7, CMH1, MPD1, CMD1S, SPMM, SPMD"	"Myosin, heavy polypeptide-7, cardiac muscle, beta"	MYH7	4625	ENSG00000092054	5'-B-4.5kb-A-3'	"Cardiomyopathy, dilated, 1S, 613426 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 1, 192600 (3), Autosomal dominant; Laing distal myopathy, 160500 (3), Autosomal dominant; Left ventricular noncompaction 5, 613426 (3), Autosomal dominant; Myopathy, myosin storage, autosomal dominant, 608358 (3), Autosomal dominant; Myopathy, myosin storage, autosomal recessive, 255160 (3), Autosomal recessive; Scapuloperoneal syndrome, myopathic type, 181430 (3), Autosomal dominant"	Myh7 (MGI:2155600)			
chr14	23415449	23417594	14q11.2	14q11.2		616096	MHRT	"Myosin heavy chain-associated RNA transcript, noncoding"	MHRT	104564225							
chr14	23417986	23418062	14q11.2	14q11.2		613613	"MIR208B, MIRN208B"	Micro RNA 208B	MIR208B	100126336							
chr14	23469688	23478192	14q11.2	14q11.2		610777	"NGDN, NGD"	Neuroguidin	NGDN	25983	ENSG00000129460			Ngdn (MGI:1916216)			
chr14	23511759	23559580	14q11.2	14q11.2		611612	THTPA	Thiamine triphosphatase	THTPA	79178	ENSG00000259431			Thtpa (MGI:2446078)			
chr14	23520854	23556314	14q11.2	14q11.2		617828	"ZFHX2, ZFH5, ZNF409, KIAA1056, KIAA1762, MARSIS"	Zinc finger homeobox 2	ZFHX2	85446	ENSG00000136367	mutation identified in 1 MARSIS family	"?Marsili syndrome, 147430 (3), Autosomal dominant"	Zfhx2 (MGI:2686934)			
chr14	23630114	23645638	14q11.2	14q11.2		615194	"DHRS2, HEP27"	"Short-chain dehydrogenase/reductase family, member 2"	DHRS2	10202	ENSG00000100867						
chr14	23938730	23955111	14q11.2	14q11.2		616925	"DHRS4AS1, AS1DHRS4, C14orf67"	"DDHRS4 antisense RNA 1, noncoding"	DHRS4-AS1	55449							
chr14	23953734	23969278	14q11.2	14q11.2		611596	"DHRS4, NRDR"	"Short-chain dehydrogenase/reductase family, member 4"	DHRS4	10901	ENSG00000157326			Dhrs4 (MGI:90169)			
chr14	23969873	24006407	14q11.2	14q11.2		615196	DHRS4L2	"Short-chain dehydrogenase/reductase family, member 4-like 2"	DHRS4L2	317749	ENSG00000187630						
chr14	24007008	24051376	14q11.2	14q11.2		615195	DHRS4L1	"Short-chain dehydrogenase/reductase family, member 4-like 1"	DHRS4L1	728635	ENSG00000225766						
chr14	24051996	24069727	14q11.2	14q11.2		614716	LRRC16B	Leucine-rich repeat-containing protein 16B	CARMIL3	90668	ENSG00000186648			Carmil3 (MGI:2448573)			
chr14	24069832	24078099	14q11.2	14q11.2		605688	CPNE6	Copine VI	CPNE6	9362	ENSG00000100884			Cpne6 (MGI:1334445)			
chr14	24078685	24115013	14q11.1-q11.2	14q11-q12		162080	"NRL, D14S46E, RP27"	Neural retina leucine zipper	NRL	4901	ENSG00000129535		"Retinal degeneration, autosomal recessive, clumped pigment type (3); Retinitis pigmentosa 27, 613750 (3), Autosomal dominant"	Nrl (MGI:102567)			
chr14	24094130	24104131	14q11.2-q12	14q11-q12		614095	"PCK2, PEPCK2"	"Phosphoenolpyruvate carboxykinase 2, mitochondrial"	PCK2	5106	ENSG00000100889		"PEPCK deficiency, mitochondrial, 261650 (1), Autosomal recessive"	Pck2 (MGI:1860456)			
chr14	24100000	57600000	14q12-q22			602086	ARVD3	Arrhythmogenic right ventricular dysplasia 3	ARVD3	424		?distinct from ARVD1	"Arrhythmogenic right ventricular dysplasia 3, 602086 (2), Autosomal dominant"				
chr14	24100000	32900000	14q12			600792	DFNB5	"Deafness, autosomal recessive 5"	DFNB5	1697			"Deafness, autosomal recessive 5, 600792 (2), Autosomal recessive"				
chr14	24100000	50400000	14q12-q21			611252	SPG32	Spastic paraplegia-32	SPG32	724107		between D14S264 and D14S978	"Spastic paraplegia 32, autosomal recessive, 611252 (2), Autosomal recessive"				
chr14	24114696	24125241	14q11.2	14q12		613317	"DCAF11, WDR23"	DDB1- and CUL4-associated factor 11	DCAF11	80344	ENSG00000100897			Dcaf11 (MGI:90168)			
chr14	24131465	24132848	14q12	14q12		612028	"FITM1, FIT1"	Fat storage-inducing transmembrane protein 1	FITM1	161247	ENSG00000139914			Fitm1 (MGI:1915930)			
chr14	24136157	24138966	14q11.2	14q12		600654	"PSME1, IFI5111"	Proteasome activator subunit-1	PSME1	5720	ENSG00000092010			Psme1 (MGI:1096367)			
chr14	24143364	24146645	14q11.2	14q12		602161	PSME2	Proteasome activator subunit-2	PSME2	5721	ENSG00000100911			Psme2 (MGI:1096365)			
chr14	24146874	24160660	14q11.2	14q12		612487	"RNF31, ZIBRA"	Ring finger protein 31	RNF31	55072	ENSG00000092098			Rnf31 (MGI:1934704)			
chr14	24161212	24166564	14q11.2	14q12		147574	"ISGF3, ISGF3G"	"Interferon-stimulated gene transcription factor 3, gamma, 48kD"	IRF9	10379	ENSG00000213928			Irf9 (MGI:107587)			
chr14	24171930	24180407	14q11.2-q12	14q12		608193	"REC8L1, REC8"	"Rec8, S. pombe, homolog of"	REC8	9985	ENSG00000100918			Rec8 (MGI:1929645)			
chr14	24205523	24208361	14q11.2	14q12		610711	"TSSK4, TSSK5"	Testis-specific serine/threonine kinase 4	TSSK4	283629	ENSG00000139908			Tssk4 (MGI:1918349)			
chr14	24209580	24213829	14q12	14q12		610051	"CHMP4A, SNF7"	"CHMP family, member 4A"	CHMP4A	29082	ENSG00000254505						
chr14	24216850	24232369	14q12	14q12		603171	NEDD8	"Neural precursor cel expressed, developmentally downregulated 8"	NEDD8	4738	ENSG00000129559			Nedd8 (MGI:97301)			
chr14	24232421	24239241	14q11-q21	14q12		610781	GMPR2	Guanosine monophosphate reductase 2	GMPR2	51292	ENSG00000100938			Gmpr2 (MGI:1917903)			
chr14	24239640	24242673	14q12	14q12		604319	"TINF2, TIN2, DKCA3"	TRF1-interacting nuclear factor 2	TINF2	26277	ENSG00000092330		"Dyskeratosis congenita, autosomal dominant 3, 613990 (3), Autosomal dominant; Revesz syndrome, 268130 (3), Autosomal dominant"	Tinf2 (MGI:107246)			
chr14	24249113	24263209	14q11.2	14q12		190195	"TGM1, ICR2, ARCI1"	"Transglutaminase-1 (K polypeptide epidermal type I, protein-glutamine gamma-glutamyltransferase)"	TGM1	7051	ENSG00000092295		"Ichthyosis, congenital, autosomal recessive 1, 242300 (3), Autosomal recessive"	Tgm1 (MGI:98730)			
chr14	24265537	24271626	14q11.2	14q12		601905	RABGGTA	"Rab geranylgeranyltransferase, alpha subunit"	RABGGTA	5875	ENSG00000100949			Rabggta (MGI:1860443)			
chr14	24290597	24299832	14q21.3	14q12		610410	DHRS1	"Short-chain dehydrogenase/reductase family, member 1"	DHRS1	115817	ENSG00000157379			Dhrs1 (MGI:1196314)			
chr14	24310150	24312052	14q11.2-q12	14q12		605773	"LTB4R2, BLTR2, BLT2"	Leukotriene B4 receptor 2	LTB4R2	56413	ENSG00000213906			Ltb4r2 (MGI:1888501)			
chr14	24311498	24318035	14q11.2-q12	14q12		601531	"LTB4R, CMKRL1, P2RY7, BLTR"	"Leukotriene b4 receptor (purinergic receptor P2Y, G protein-coupled, 7; chemokine receptor-like 1)"	LTB4R	1241	ENSG00000213903			Ltb4r1 (MGI:1309472)			
chr14	24318348	24335070	14q11.2	14q12		600292	ADCY4	Adenylate cyclase-4	ADCY4	196883	ENSG00000129467			Adcy4 (MGI:99674)			
chr14	24336020	24340035	14q11.2	14q12		605817	"RIPK3, RIP3"	Receptor-interacting serine/threonine kinase 3	RIPK3	11035	ENSG00000129465			Ripk3 (MGI:2154952)			
chr14	24366910	24379603	Chr.14	14q12		602699	NFATC4	"Nuclear factor of activated T cells, cytoplasmic, calcineurin-dependent 4"	NFATC4	4776	ENSG00000100968			Nfatc4 (MGI:1920431)			
chr14	24426531	24429524	14q12	14q12		612978	CBLN3	Precerebellin 3	CBLN3	643866	ENSG00000139899			Cbln3 (MGI:1889286)			
chr14	24439764	24442904	14q12	14q12		616162	SDR39U1	"Short-chain dehydrogenase/reductase family 39U, member 1"	SDR39U1	56948	ENSG00000100445			Sdr39u1 (MGI:1916876)			
chr14	24505354	24508264	14q11.2	14q12		118938	CMA1	"Chymase-1, mast cell"	CMA1	1215	ENSG00000092009			Cma1 (MGI:96941)			
chr14	24573517	24576259	14q11.2	14q12		116830	CTSG	Cathepsin G	CTSG	1511	ENSG00000100448			Ctsg (MGI:88563)			
chr14	24606479	24609762	14q11.2	14q12		116831	"GZMH, CTSGL2"	Granzyme H (cathepsin G-like 2)	GZMH	2999	ENSG00000100450			"Gzmd,Gzme,Gzmf,Gzmg (MGI:109253,MGI:109255,MGI:109265,MGI:109254)"			
chr14	24630953	24634268	14q11.2	14q12		123910	"GZMB, CTLA1, CSPB"	Granzyme B (cytotoxic T-lymphocyte-associated serine esterase-1; cathepsin G-like 1)	GZMB	3002	ENSG00000100453						
chr14	24809653	25050296	14q12	14q12		607958	"STXBP6, AMISYN, HSPC156"	Syntaxin-binding protein 6	STXBP6	29091	ENSG00000168952			Stxbp6 (MGI:2384963)			
chr14	26445882	26597753	14q12	14q12		602157	NOVA1	NOVA alternative splicing regulator 1	NOVA1	4857	ENSG00000139910			Nova1 (MGI:104297)			
chr14	28767071	28770276	14q13	14q12		164874	"FOXG1, FOXG1B, FKHL1, FKH2, QIN, BF1"	Forkhead box G1B	FOXG1	2290	ENSG00000176165		"Rett syndrome, congenital variant, 613454 (3), Autosomal dominant"	Foxg1 (MGI:1347464)			
chr14	29576478	29927804	14q12	14q12		605435	"PRKD1, PRKCM, PKD, CHDED"	Protein kinase D1	PRKD1	5587	ENSG00000184304		"Congenital heart defects and ectodermal dysplasia, 617364 (3), Autosomal dominant"	Prkd1 (MGI:99879)			
chr14	30559122	30620063	14q12	14q12		611299	"G2E3, KIAA1333"	G2/M phase-specific E3 ubiquitin ligase	G2E3	55632	ENSG00000092140			G2e3 (MGI:2444298)			
chr14	30874495	30890617	14q12-q13	14q12		603196	"COCH, DFNA9"	Cochlin	COCH	1690	ENSG00000100473		"Deafness, autosomal dominant 9, 601369 (3), Autosomal dominant"	Coch (MGI:1278313)			
chr14	30893798	31026400	14q12	14q12		614766	"STRN3, SG2NA"	"Striatin, calmodulin-binding protein 3"	STRN3	29966	ENSG00000196792			Strn3 (MGI:2151064)			
chr14	31025105	31096449	14q12	14q12		607243	"AP4S1, CPSQ6, SPG52"	"Adaptor-related protein complex 4, sigma-1 subunit"	AP4S1	11154	ENSG00000100478		"Spastic paraplegia 52, autosomal recessive, 614067 (3), Autosomal recessive"	Ap4s1 (MGI:1337065)			
chr14	31482943	31487944	14q12	14q12		610118	GPR33	G protein-coupled receptor 33	GPR33	2856	ENSG00000214943			Gpr33 (MGI:1277106)			
chr14	31561384	31861292	14q12	14q12		613621	"NUBPL, IND1"	Nucleotide-binding protein-like protein	NUBPL	80224	ENSG00000151413		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Nubpl (MGI:1924076)			
chr14	32072587	32159727	14q12	14q12		602680	"ARHGAP5, RHOGAP5"	RHO GTPase-activating protein 5	ARHGAP5	394	ENSG00000100852			Arhgap5 (MGI:1332637)			
chr14	32203609	32833998	14q	14q12		604691	"ADAP6, ADAP100"	A-kinase anchor protein 6	AKAP6	9472	ENSG00000151320			Akap6 (MGI:3050566)			
chr14	32900000	37400000	14q13			609408	HPE8	Holoprosencephaly 8		619406		between D14S49 and D14S1014	"Holoprosencephaly 8, 609408 (2)"				
chr14	32900000	50400000	14q13-q21			608831	RLS2	"Restless legs syndrome, susceptibility to, 2"		450097		max lod at D14S288	"{Restless legs syndrome 2}, 608831 (2)"				
chr14	32934784	33804175	14q13	14q13.1		609430	"NPAS3, MOP6"	Neuronal PAS domain protein 3	NPAS3	64067	ENSG00000151322			Npas3 (MGI:1351610)			
chr14	33924214	33951077	14q13.1	14q13.1		606426	"EGLN3, PHD3, HIFP4H3"	"Egl9, C. elegans, homolog of, 3"	EGLN3	112399	ENSG00000129521			Egln3 (MGI:1932288)			
chr14	34432937	34462261	14q13.1	14q13.1		613540	"SPTSSA, C14orf147, SSSPTA"	"Serine palmitoyltransferase, small subunit, A"	SPTSSA	171546	ENSG00000165389			Sptssa (MGI:1913399)			
chr14	34561092	34630182	14q13.1	14q13.1		606098	SNX6	Sorting nexin 6	SNX6	58533	ENSG00000129515			Snx6 (MGI:1919433)			
chr14	34710381	34714822	14q12	14q13.1		601443	"CFL2, NEM7"	"Cofilin 2, muscle"	CFL2	1073	ENSG00000165410		"Nemaline myopathy 7, autosomal recessive, 610687 (3), Autosomal recessive"	Cfl2 (MGI:101763)			
chr14	34752730	34875646	14q12-q13	14q13.1-q13.2		605680	BAZ1A	"Bromodomain adjacent to zinc finger domain, 1A"	BAZ1A	11177	ENSG00000198604			Baz1a (MGI:1309478)			
chr14	34982897	35029566	14q13.2	14q13.2		604857	SRP54	"Signal recognition particle, 54kD"	SRP54	6729	ENSG00000100883			"Srp54a,Srp54b (MGI:3714357,MGI:1346087)"			
chr14	35085466	35122661	14q13.2	14q13.2		615902	"PPP2RC2, G5PR"	"Protein phosphatase 2, regulatory subunit B-double prime, gamma"	PPP2R3C	55012	ENSG00000092020			Ppp2r3c (MGI:1930009)			
chr14	35122302	35274077	14q13	14q13.2		609947	KIAA0391	KIAA0391 gene	KIAA0391	9692	ENSG00000100890			1110008L16Rik (MGI:1913382)			
chr14	35278557	35317478	14q13	14q13.2		602855	"PSMA6, PROS27, P27K"	"Proteasome subunit, alpha-type, 6"	PSMA6	5687	ENSG00000100902		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Psma6 (MGI:1347006)			
chr14	35401509	35404753	14q13	14q13.2		164008	"NFKBIA, IKBA"	"Nuclear factor of kappa light chain gene enhancer in B-cells inhibitor, alpha"	NFKBIA	4792	ENSG00000100906		"Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, 612132 (3), Autosomal dominant"	Nfkbia (MGI:104741)			
chr14	35534041	35537053	14q13.2	14q13.2		614027	"INSM2, IA6"	Insulinoma-associated 2	INSM2	84684	ENSG00000168348			Insm2 (MGI:1930787)			
chr14	35538351	35809322	14q13.2	14q13.2		608884	"RALGAPA1, GARNL1, TULIP1, GRIPE, KIAA0884"	"Ral GTPase activating protein, alpha subunit 1 (catalytic)"	RALGAPA1	253959	ENSG00000174373	pseudogene on 9q31.1		Ralgapa1 (MGI:1931050)			
chr14	36100000	43000000	14q13.3-q21.1			604461	HPV6AI1	Human papillomavirus type 6A integration site 1	HPV6AI1	3259		previously assigned to 10q24					
chr14	36135709	36176650	14q13.3	14q13.3		614821	PTCSC3	PTCSC3 gene	PTCSC3	100886964							
chr14	36298557	36320675	14q13.3	14q13.3		609431	MBIP	MAP3K12-binding inhibitory protein	MBIP	51562	ENSG00000151332			Mbip (MGI:1918320)			
chr14	36473287	36519520	14q13.3	14q13.3		617860	"SFTA3, SPH"	Surfactant-associated protein 3	SFTA3	253970	ENSG00000229415						
chr14	36516396	36520224	14q13	14q13.3		600635	"NKX2-1, TITF1, NKX2A, TTF1, NMTC1"	NK2 homeobox 1	NKX2-1	7080	ENSG00000136352		"Chorea, hereditary benign, 118700 (3), Autosomal dominant; Choreoathetosis, hypothyroidism, and neonatal respiratory distress, 610978 (3), Autosomal dominant; {Thyroid cancer, nonmedullary, 1}, 188550 (3), Autosomal dominant"	Nkx2-1 (MGI:108067)			
chr14	36580010	36582613	14q12-q13	14q13.3		603245	"NKX2-8, NKX2H, NKX2.8"	NK2 homeobox 8	NKX2-8	26257	ENSG00000136327			Nkx2-9 (MGI:1270158)			
chr14	36657567	36677806	14q12-q13	14q13.3		167416	"PAX9, STHAG3"	Paired box gene 9	PAX9	5083	ENSG00000198807		"Tooth agenesis, selective, 3, 604625 (3), Autosomal dominant"	Pax9 (MGI:97493)			
chr14	36677317	37172659	14q11.2	14q13.3		607571	"SLC25A21, ODC"	"Solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21"	SLC25A21	89874	ENSG00000183032			Slc25a21 (MGI:2445059)			
chr14	37197887	37579206	14q13	14q13.3-q21.1		606850	MIPOL1	MIPOL1 gene	MIPOL1	145282	ENSG00000151338			Mipol1 (MGI:1920740)			
chr14	37589551	37595119	14q13	14q21.1		602294	"FOXA1, HNF3A"	"Forkhead box A1 (hepatocyte nuclear factor-3, alpha)"	FOXA1	3169	ENSG00000129514			Foxa1 (MGI:1347472)			
chr14	38207998	38213062	14q13	14q21.1		182451	SSTR1	Somatostatin receptor-1	SSTR1	6751	ENSG00000139874			Sstr1 (MGI:98327)			
chr14	38253999	38256369	14q21.1	14q21.1		616845	CLEC14A	"C-type lectin domain family 14, member A"	CLEC14A	161198	ENSG00000176435			Clec14a (MGI:1914114)			
chr14	39031918	39103527	14q21.1	14q21.1		610511	"SEC23A, CLSD"	"Sec23, S. cerevisiae, homolog of, A"	SEC23A	10484	ENSG00000100934		"Craniolenticulosutural dysplasia, 607812 (3), Autosomal recessive"	Sec23a (MGI:1349635)			
chr14	39114260	39136972	14q21.1	14q21.1		602595	"GEMIN2, SIP1"	GEM-associated protein 2	GEMIN2	8487	ENSG00000092208			Gemin2 (MGI:1913853)			
chr14	39147810	39170429	14q21.1	14q21.1		610397	"TRAPPC6B, TPC6, NEDMEBA"	"Trafficking protein particle complex, subunit 6B"	TRAPPC6B	122553	ENSG00000182400		"Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy, 617862 (3)"	Trappc6b (MGI:1925482)			
chr14	39175182	39183217	Chr.14	14q21.1		603154	"PNN, DRS"	Pinin	PNN	5411	ENSG00000100941			Pnn (MGI:1100514)			
chr14	39233915	39388512	14q	14q21.1		602132	"MGEA, MEA6"	Meningioma-expressed antigen 6	MIA2	4253	ENSG00000150527	?pseudogenes on other chromosomes					
chr14	39396372	39432499	14q13.3	14q21.1		609103	"FBXO33, FBX33, BMND12"	F-box only protein 33	FBXO33	254170	ENSG00000165355			Fbxo33 (MGI:1917861)			
chr14	41606855	41904548	14q21.2	14q21.1		612811	"LRFN5, SALM5"	Leucine-rich repeat and fibronectin type III domain-containing protein 5	LRFN5	145581	ENSG00000165379			Lrfn5 (MGI:2144814)			
chr14	43000000	57600000	14q21.2-q22.3			607501	"MGR4, MGOA"	"Migraine without aura, susceptibility to, 4"		338342		between D14S976 and D14S978	"{Migraine without aura, susceptibility to, 4}, 607501 (2), Autosomal dominant"				
chr14	44504148	44507295	14q21.3	14q21.2		611779	"FSCB, C14orf155"	Fibrous sheath cabyr-binding protein	FSCB	84075	ENSG00000189139						
chr14	44962189	45074430	14q21.2	14q21.2		617618	"TOGARAM1, FAM179B, KIAA0423"	TOG array regulator of axonemal microtubules 1	TOGARAM1	23116	ENSG00000198718			Togaram1 (MGI:2684313)			
chr14	45084098	45115600	14q21.2	14q21.2		614907	PRPF39	"Precursor mRNA-processing factor 39, S. cerevisiae, homolog of"	PRPF39	55015	ENSG00000185246			Prpf39 (MGI:104602)			
chr14	45115291	45134528	14q21.2	14q21.2		186947	"FKBP3, FKBP25"	FK506-binding protein 3	FKBP3	2287	ENSG00000100442			Fkbp3 (MGI:1353460)			
chr14	45135938	45200889	14q21.3	14q21.2		609644	"FANCM, KIAA1596"	FANCM gene	FANCM	57697	ENSG00000187790			Fancm (MGI:2442306)			
chr14	46836517	47675315	14q21	14q21.3		611128	MDGA2	MAM domain-containing glycosylphosphatidylinositol anchor 2	MDGA2	161357	ENSG00000139915			Mdga2 (MGI:2444706)			
chr14	49570983	49598709	14q	14q21.3		603633	"RPS29, DBA13"	Ribosomal protein S29	RPS29	6235	ENSG00000213741		"Diamond-Blackfan anemia 13, 615909 (3), Autosomal dominant"	Rps29 (MGI:107681)			
chr14	49586579	49586877	14q22.1	14q21.3		612177	"RN7SL1, 7SL, 7L1A"	"RNA, 7SL, cytoplasmic 1"	RN7SL1	6029							
chr14	49618687	49620684	Chr.14	14q21.3		180469	"RPL36AL, RPL36A"	Ribosomal protein L36a-like	RPL36AL	6166	ENSG00000165502			Rpl36al (MGI:1913733)			
chr14	49620770	49623480	14q21	14q21.3		602616	"MGAT2, CDGS2, CDG2A"	"Mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyl- transferase"	MGAT2	4247	ENSG00000168282		"Congenital disorder of glycosylation, type IIa, 212066 (3), Autosomal recessive"	Mgat2 (MGI:2384966)			
chr14	49625173	49635229	14q21.3	14q21.3		612517	"KTU, C14orf104, CILD10"	"Kintoun, Medaka, homolog of"	DNAAF2	55172	ENSG00000165506		"Ciliary dyskinesia, primary, 10, 612518 (3)"	Dnaaf2 (MGI:1923566)			
chr14	49643551	49688416	14q13-q21	14q21.3		602670	"POLE2, DPE2"	"Polymerase, DNA, epsilon-2"	POLE2	5427	ENSG00000100479			Pole2 (MGI:1197514)			
chr14	49690461	49753151	14q21.3	14q21.3		611281	KLHDC1	KELCH domain-containing protein 1	KLHDC1	122773	ENSG00000197776			Klhdc1 (MGI:2672853)			
chr14	49767607	49786384	14q21.3	14q21.3		611280	"KLHDC2, HCLP1"	KELCH domain-containing protein 2	KLHDC2	23588	ENSG00000165516			Klhdc2 (MGI:1916804)			
chr14	49782082	49853202	14q22	14q21.3		608378	"NEMF, SDCCAG1"	Nuclear export mediator factor	NEMF	9147	ENSG00000165525			Nemf (MGI:1918305)			
chr14	49853615	49853913	14q22.1	14q21.3		612180	RN7SL3	"RNA, 7SL, cytoplasmic 3"	RN7SL3	378707							
chr14	49862550	49862848	14q22.1	14q21.3		612179	"RN7SL2, 7L1C"	"RNA, 7SL, cytoplasmic 2"	RN7SL2	378706							
chr14	49893017	49897053	14q21.3	14q21.3		600464	ARF6	ADP-ribosylation factor 6	ARF6	382	ENSG00000165527			Arf6 (MGI:99435)			
chr14	50100455	50116578	14q21.3	14q21.3		615260	"VCPKMT, METTL21D, C14orf138"	Valosin-containing protein lysine methyltransferase	VCPKMT	79609	ENSG00000100483			Vcpkmt (MGI:2684917)			
chr14	50117118	50231692	14q21	14q21.3		601247	"SOS2, NS9"	"Son of sevenless, Drosophila, homolog of, 2"	SOS2	6655	ENSG00000100485		"Noonan syndrome 9, 616559 (3), Autosomal dominant"	Sos2 (MGI:98355)			
chr14	50242433	50312228	14q22.1	14q21.3		609584	"L2HGDH, C14orf160, L2HGA"	L-2-hydroxyglutarate dehydrogenase	L2HGDH	79944	ENSG00000087299		"L-2-hydroxyglutaric aciduria, 236792 (3), Autosomal recessive"	L2hgdh (MGI:2384968)			
chr14	50329403	50397403	14q21.3	14q21.3		603441	"CDKL1, KKIALRE, p42"	Cyclin-dependent kinase-like 1	CDKL1	8814	ENSG00000100490			Cdkl1 (MGI:1918341)			
chr14	50400000	67400000	14q22-q23			115650	"CTRCT32, CTAA1, CAP, CTPP5"	"Cataract 32, multiple types"	CTAA1	1483		between D14S980 and D14S1069	"Cataract 32, multiple types, 115650 (2), Autosomal dominant"				
chr14	50400000	57600000	14q22.1-q22.3			609640	"FRIASS, DEL14q22, C14DELq22"	Frias syndrome				deletion spans 4.1 Mb on 14q22.1-q22.3	"Frias syndrome, 609640 (4), Autosomal dominant"				
chr14	50400000	73300000	14q22.1-q24.2			255500	MYP18	Myopia 18	MYP18	100359406		between D14S984 and D14S999	"Myopia 18, 255500 (2), Autosomal recessive"				
chr14	50533081	50633067	14q11-q21	14q22.1		606439	"ATL1, SPG3A, HSN1D"	Atlastin GTPase 1	ATL1	51062	ENSG00000198513		"Neuropathy, hereditary sensory, type ID, 613708 (3), Autosomal dominant; Spastic paraplegia 3A, autosomal dominant, 182600 (3), Autosomal dominant"	Atl1 (MGI:1921241)			
chr14	50418491	50561125	Chr.14	14q22.1		604923	"MAP4K5, MAPKKKK5"	Mitogen-activated protein kinase kinase kinase kinase-5	MAP4K5	11183	ENSG00000012983			Map4k5 (MGI:1925503)			
chr14	50633103	50668352	14q13-q23	14q22.1		607203	"WW45, SAV"	"WW domain-containing protein, 45kD"	SAV1	60485	ENSG00000151748			Sav1 (MGI:1927144)			
chr14	50719762	50831139	14q22.1	14q22.1		608684	"NIN, KIAA1565, SCKL7"	Ninein	NIN	51199	ENSG00000100503	mutation identified in 1 SCKL7 family	"?Seckel syndrome 7, 614851 (3), Autosomal recessive"	Nin (MGI:105108)			
chr14	50905216	50944529	14q22.1	14q22.1		613741	PYGL	"Phosphorylase, glycogen, liver"	PYGL	5836	ENSG00000100504		"Glycogen storage disease VI, 232700 (3), Autosomal recessive"	Pygl (MGI:97829)			
chr14	50975260	51105172	14q21-q24	14q22.1		606555	"TRIM9, SPRING, KIAA0282"	Tripartite motif-containing protein 9	TRIM9	114088	ENSG00000100505			Trim9 (MGI:2137354)			
chr14	51240167	51257654	14q22.1	14q22.1		610527	"TXNDC1, TMX"	Thioredoxin domain-containing 1	TMX1	81542	ENSG00000139921			Tmx1 (MGI:1919986)			
chr14	51489099	51730726	14q22.1	14q22.1		614555	"FRMD6, WILLIN, C14orf31"	FERM domain-containing protein 6	FRMD6	122786	ENSG00000139926			Frmd6 (MGI:2442579)			
chr14	51847130	51969799	14q21	14q22.1		606981	GNG2	"Guanine nucleotide-binding protein, gamma-2"	GNG2	54331	ENSG00000186469			Gng2 (MGI:102705)			
chr14	51989509	52004701	14q22.1	14q22.1		610858	"C14orf166, CGI99"	Chromosome 14 open reading frame 166	RTRAF	51637	ENSG00000087302			Rtraf (MGI:1915295)			
chr14	52004801	52069227	Chr.14	14q22.1		605399	NID2	Nidogen 2	NID2	22795	ENSG00000087303			Nid2 (MGI:1298229)			
chr14	52267255	52276723	14q22.1	14q22.1		604687	"PTGDR, AS1, ASRT1"	Prostaglandin D2 receptor	PTGDR	5729	ENSG00000168229		"{Asthma, susceptibility to, 1}, 607277 (3)"	Ptgdr (MGI:102966)			
chr14	52314297	52328605	14q22	14q22.1		176804	PTGER2	"Prostaglandin E receptor 2, EP2 subtype, 53kD"	PTGER2	5732	ENSG00000125384		"{Asthma, aspirin-induced, susceptibility to}, 208550 (3), Autosomal recessive"	Ptger2 (MGI:97794)			
chr14	52430589	52552582	14q22.1	14q22.1		616179	"TXNDC16, KIAA1344"	Thioredoxin domain-containing protein 16	TXNDC16	57544	ENSG00000087301			Txndc16 (MGI:1917811)			
chr14	52639914	52695930	14q22.1	14q22.1		615435	"ERO1L, ERO1LA"	Endoplasmic reticulum oxidoreduction 1-like	ERO1A	30001	ENSG00000197930			Ero1l (MGI:1354385)			
chr14	52707156	52727997	14q22.1	14q22.1		602708	PSMC6	"Proteasome 26S subunit, ATPase, 6"	PSMC6	5706	ENSG00000100519	previously assigned to 12q15 by FISH		Psmc6 (MGI:1914339)			
chr14	52730158	52774988	14q22.1	14q22.1		615814	STYX	Serine/threonine/tyrosine-interacting protein	STYX	6815	ENSG00000198252			Styx (MGI:1891150)			
chr14	52775192	52791667	14q22.1	14q22.1		616510	"GNPNAT1, GNA1"	Glucosamine-phosphate N-acetyltransferase 1	GNPNAT1	64841	ENSG00000100522			Gnpnat1 (MGI:1858963)			
chr14	52857270	52951096	14q22.1	14q22.1		607746	"FERMT2, PLEKHC1, MIG2, UNC112, KIND2"	"Fermitin family, Drosophila, homolog of, 2"	FERMT2	10979	ENSG00000073712			Fermt2 (MGI:2385001)			
chr14	53036739	53153327	14q22.1	14q22.1		614603	"DDHD1, PAPLA1, KIAA1705, SPG28"	DDHD domain-containing protein 1	DDHD1	80821	ENSG00000100523		"Spastic paraplegia 28, autosomal recessive, 609340 (3), Autosomal recessive"	Ddhd1 (MGI:2150302)			
chr14	53600000	55000000	14q22.2			612589	CRCS8	"Colorectal cancer, susceptibility to, 8"		100271690		associated with rs4444235	"{Colorectal cancer, susceptibility to, 8}, 612589 (2)"				
chr14	53949735	53956890	14q22.2	14q22.2		112262	"BMP4, BMP2B1, BMP2B, MCOPS6, OFC11"	Bone morphogenetic protein-4	BMP4	652	ENSG00000125378		"Microphthalmia, syndromic 6, 607932 (3), Autosomal dominant; Orofacial cleft 11, 600625 (3)"	Bmp4 (MGI:88180)			
chr14	54396867	54420217	14q22	14q22.2		123832	CDKN3	Cyclin-dependent kinase inhibitor 3 (CDK2-associated dual specificity phosphatase)	CDKN3	1033	ENSG00000100526			Cdkn3 (MGI:1919641)			
chr14	54426928	54441429	14q22.2	14q22.2		611287	"CNIH, TGAM77"	"Cornichon, Drosophila, homolog of"	CNIH1	10175	ENSG00000100528			Cnih1 (MGI:1277202)			
chr14	54474490	54489025	14q22.2	14q22.2		601713	"GMFB, GMF"	"Glia maturation factor, beta"	GMFB	2764	ENSG00000197045			Gmfb (MGI:1927133)			
chr14	54509868	54539309	14q22.1	14q22.2		606138	"GCRRF1, CGR19"	Cell growth regulator with ring finger domain 1	CGRRF1	10668	ENSG00000100532			Cgrrf1 (MGI:1916368)			
chr14	54567096	54793314	14q22.2	14q22.2		610747	"SAMD4A, SMAUG1, KIAA1053"	Sterile alpha motif domain-containing 4A	SAMD4A	23034	ENSG00000020577			Samd4 (MGI:1921730)			
chr14	54842004	54902823	14q22.1-q22.2	14q22.2		600225	"GCH1, DYT5, HPABH4B"	GTP cyclohydrolase 1	GCH1	2643	ENSG00000131979		"Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, 128230 (3), Autosomal recessive, Autosomal dominant; Hyperphenylalaninemia, BH4-deficient, B, 233910 (3), Autosomal recessive"	Gch1 (MGI:95675)			
chr14	54938937	55027105	14q22.2	14q22.2-q22.3		608126	"WDHD1, AND1"	WD repeat and HMG-box DNA binding protein 1	WDHD1	11169	ENSG00000198554			Wdhd1 (MGI:2443514)			
chr14	55027125	55049488	14q22.3	14q22.3		616337	"SOCS4, SOCS7"	Suppressor of cytokine signaling 4	SOCS4	122809	ENSG00000180008			Socs4 (MGI:1914546)			
chr14	55051643	55070193	14q22.3	14q22.3		617226	"MAP1IP1L, MISS"	Mitogen-activated protein kinase 1-interacting protein 1-like protein	MAPK1IP1L	93487	ENSG00000168175			Mapk1ip1l (MGI:2444022)			
chr14	55129216	55145429	14q21-q22	14q22.3		153619	"LGALS3, MAC2, GALBP"	"Lectin, galactose-binding, soluble, 3"	LGALS3	3958	ENSG00000131981	assigned earlier to 1p13		Lgals3 (MGI:96778)			
chr14	55148115	55191677	14q22.3	14q22.3		617859	"DLGAP5, DLG7, HURP, KIAA0008"	Discs large-associated protein 5	DLGAP5	9787	ENSG00000126787			Dlgap5 (MGI:2183453)			
chr14	55229192	55229935	14q24.3	14q22.3		600012	"UBE2L1, UBCL, UBC4"	Ubiquitin-conjugating enzyme E2L 1	UBE2L1	283556							
chr14	55271302	55353610	14q22.2	14q22.3		609104	"FBXO34, FBX34"	F-box only protein 34	FBXO34	55030	ENSG00000178974			Fbxo34 (MGI:1926188)			
chr14	55366390	55411857	14q22.3	14q22.3		613515	"ATG14, ATG14L, KIAA0831, BARKOR"	"Autophagy 14, S. cerevisiae, homolog of"	ATG14	22863	ENSG00000126775			Atg14 (MGI:1261775)			
chr14	55580206	55684583	14q22	14q22.3		600381	"KTN1, CG1"	Kinectin	KTN1	3895	ENSG00000126777						
chr14	56118328	56301585	14q21	14q22.3		614798	PELI2	"Pellino, Drosophila, homolog of, 2"	PELI2	57161	ENSG00000139946			Peli2 (MGI:1891445)			
chr14	56579791	56660628	14q22.3	14q22.3		617449	"TMEM260, C14orf101, SHDRA"	Transmembrane protein 260	TMEM260	54916	ENSG00000070269		"Structural heart defects and renal anomalies syndrome, 617478 (3), Autosomal recessive"	Tmem260 (MGI:2443219)			
chr14	56800706	56810475	14q22.3	14q22.3		600037	"OTX2, MCOPS5, CPHD6"	"Orthodenticle, Drosophila, homolog of, 2"	OTX2	5015	ENSG00000165588		"Microphthalmia, syndromic 5, 610125 (3), Autosomal dominant; Pituitary hormone deficiency, combined, 6, 613986 (3), Autosomal dominant; Retinal dystrophy, early-onset, with or without pituitary dysfunction, 610125 (3), Autosomal dominant"	Otx2 (MGI:97451)			
chr14	57202475	57268898	14q22.3	14q22.3		604469	"EXOC5, SEC10L1"	Exocyst complex component 5	EXOC5	10640	ENSG00000070367			Exoc5 (MGI:2145645)			
chr14	57268887	57298741	14q22.3	14q22.3		614368	"AP5M1, MUDENG, MUD, C14orf108"	"Adaptor-related protein complex 5, mu-1 subunit"	AP5M1	55745	ENSG00000053770			Ap5m1 (MGI:1921635)			
chr14	57600000	67400000	14q23			612162	ANIB8	"Aneurysm, intracranial berry, 8"		100188886		associated with rs767603	"Aneurysm, intracranial berry, 8, 612162 (2)"				
chr14	57600000	67400000	14q23			606972	EIG2	"Epilepsy, idiopathic generalized, susceptibility to, 2"		353124			"{Epilepsy, idiopathic generalized, susceptibility to, 2}, 606972 (2)"				
chr14	58244804	58272008	14q23	14q23.1		176843	PSMA3	"Proteasome (prosome, macropain) subunit, alpha type, 3"	PSMA3	5684	ENSG00000100567			Psma3 (MGI:104883)			
chr14	58298384	58373732	14q23.1	14q23.1		180201	"ARID4A, RBP1, RBBP1"	AT-rich interactive domain-containing protein 4A	ARID4A	5926	ENSG00000032219			Arid4a (MGI:2444354)			
chr14	58408493	58427613	14q21	14q23.1		607384	"TIMM9, TIM9"	"Translocase of inner mitochondrial membrane 9, yeast, homolog of"	TIMM9	26520	ENSG00000100575			Timm9 (MGI:1353436)			
chr14	58427384	58548830	14q23.1	14q23.1		610178	"KIAA0586, TALPID3, JBTS23, SRTD14"	KIAA0586 gene	KIAA0586	9786	ENSG00000100578		"Joubert syndrome 23, 616490 (3), Autosomal recessive; Short-rib thoracic dysplasia 14 with polydactyly, 616546 (3), Autosomal recessive"	2700049A03Rik (MGI:1924217)			
chr14	58634067	58648320	14q22.3	14q23.1		607861	"DACT1, DPR1, DAPPER1, FRODO, TBS2"	"Dapper, antagonist of beta-catenin, 1"	DACT1	51339	ENSG00000165617	mutation identified in 1 TBS2 family	"?Townes-Brocks syndrome 2, 617466 (3), Autosomal dominant"	Dact1 (MGI:1891740)			
chr14	59188656	59371404	14q23.1	14q23.1		606626	"DAAM1, KIAA0666"	Dishevelled-associated activator of morphogenesis 1	DAAM1	23002	ENSG00000100592			Daam1 (MGI:1914596)			
chr14	59452772	59465635	14q23.1	14q23.1		607970	GPR135	G protein-coupled receptor 135	GPR135	64582	ENSG00000181619			Gpr135 (MGI:2676315)			
chr14	59472610	59505265	14q23.1	14q23.1		614811	"L3HYPDH, C14orf149"	"L-3-hydroxyproline dehydratase, trans"	L3HYPDH	112849	ENSG00000126790			L3hypdh (MGI:1914467)			
chr14	59484442	59505406	14q23.1	14q23.1		611176	"JKAMP, C24orf100, JAMP"	JNK1/MAPK8-associated membrane protein	JKAMP	51528	ENSG00000050130			Jkamp (MGI:1915057)			
chr14	59595975	59871287	14q21-q22	14q23.1		600865	"RTN1, NSP"	Reticulon 1 (neuroendocrine-specific protein)	RTN1	6252	ENSG00000139970			Rtn1 (MGI:1933947)			
chr14	60144118	60169863	14q23.1	14q23.1		612833	"DHRS7, RETSDR4"	"Short-chain dehydrogenase/reductase family, member 7"	DHRS7	51635	ENSG00000100612			Dhrs7 (MGI:1913625)			
chr14	60245751	60299086	14q23.1	14q23.1		606108	"PPM1A, PP2CA"	"Protein phosphatase, magnesium/manganese-dependent, 1A"	PPM1A	5494	ENSG00000100614			Ppm1a (MGI:99878)			
chr14	60435953	60499773	14q23.1	14q23.1		617307	"C14orf39, SIX6OS1"	Chromosome 14 open reading frame 39	C14orf39	317761	ENSG00000179008			4930447C04Rik (MGI:1923051)			
chr14	60509219	60511806	14q23	14q23.1		606326	"SIX6, ODRMD"	"Sine oculis homeo box, Drosophila, homolog of, 6"	SIX6	4990	ENSG00000184302		"Optic disc anomalies with retinal and/or macular dystrophy, 212550 (3), Autosomal recessive"	Six6 (MGI:1341840)			
chr14	60644698	60649488	14q23	14q23.1		601205	"SIX1, BOS3, DFNA23"	"Sine oculis homeo box, Drosophila, homolog of, 1"	SIX1	6495	ENSG00000126778		"Branchiootic syndrome 3, 608389 (3), Autosomal dominant; Deafness, autosomal dominant 23, 605192 (3), Autosomal dominant"	Six1 (MGI:102780)			
chr14	60709537	60724320	14q23	14q23.1		606342	SIX4	"Sine oculis homeo box, Drosophila, homolog of, 4"	SIX4	51804	ENSG00000100625			Six4 (MGI:106034)			
chr14	60734734	60969880	14q23	14q23.1		602659	"MNAT1, MAT1"	Menage a trois 1	MNAT1	4331	ENSG00000020426			Mnat1 (MGI:106207)			
chr14	60971440	60981689	14q23.1	14q23.1		611023	"TRMT5, TRM5, KIAA1393, COXPD26"	"tRNA methyltransferase 5, S. cerevisiae, homolog of"	TRMT5	57570	ENSG00000126814		"Combined oxidative phosphorylation deficiency 26, 616539 (3), Autosomal recessive"	Trmt5 (MGI:1923607)			
chr14	60981113	61083732	14q23.1	14q23.1		616518	"SLC38A6, SNAT6"	"Solute carrier family 38 (amino acid transporter), member 6"	SLC38A6	145389	ENSG00000139974			Slc38a6 (MGI:3648156)			
chr14	61187304	61550979	14q22-q23	14q23.1		605437	"PRKCH, PKCL, PRKCL"	"Protein kinase C, eta"	PRKCH	5583	ENSG00000027075		"{Cerebral infarction, susceptibility to}, 601367 (3), Multifactorial"	Prkch (MGI:97600)			
chr14	61277369	61281811	14q23.1	14q23.1		611029	"TMEM30B, CDC50B"	Transmembrane protein 30B	TMEM30B	161291	ENSG00000182107			Tmem30b (MGI:2442082)			
chr14	61600000	64300000	14q23.2			609113	TELM	"Telomere length, mean leukocyte"		550641		"suggestive QTL on 12, 10q, 3p"	"[Telomere length, mean leukocyte], 609113 (2)"				
chr14	61681040	61695822	14q23.2	14q23.2		614528	HIF1AAS1	HIF1A antisense RNA 1	HIF1A-AS1	100750246							
chr14	61695400	61748258	14q21-q24	14q23.2		603348	"HIF1A, MOP1"	"Hypoxia-inducible factor 1, alpha subunit"	HIF1A	3091	ENSG00000100644			Hif1a (MGI:106918)			
chr14	61747038	61749088	14q23.2	14q23.2		614529	HIF1AAS2	HIF1A antisense RNA 2	HIF1A-AS2	100750247							
chr14	61762356	61796427	14q23.2	14q23.2		600591	"SNAPC1, SNAP43"	"Small nuclear RNA-activating protein complex, polypeptide 1"	SNAPC1	6617	ENSG00000023608			Snapc1 (MGI:1922877)			
chr14	61812155	62112824	14q23.1	14q23.2		610950	"SYT16, STREP14"	Synaptotagmin 16	SYT16	83851	ENSG00000139973			Syt16 (MGI:2673872)			
chr14	62706572	63045237	14q23.2	14q23.2		605716	KCNH5	"Potassium voltage-gated channel, subfamily H, member 5"	KCNH5	27133	ENSG00000140015			Kcnh5 (MGI:3584508)			
chr14	63204383	63293511	14q23.2	14q23.2		607653	"RHOJ, ARHJ, TCL"	"Ras homolog gene family, member J"	RHOJ	57381	ENSG00000126785			Rhoj (MGI:1931551)			
chr14	63312834	63318878	14q23.2	14q23.2		609652	"GPHB5, GPB5"	"Glycoprotein hormone, beta-5"	GPHB5	122876	ENSG00000179600			Gphb5 (MGI:2156540)			
chr14	63371355	63543394	14q23.1	14q23.2		601647	PPP2R5E	"Protein phosphatase-2, regulatory subunit B (B56), epsilon isoform"	PPP2R5E	5529	ENSG00000154001	incorrectly assigned to 7p12-p11.2 by FISH		Ppp2r5e (MGI:1349473)			
chr14	63684215	63728107	14q22.1	14q23.2		612826	"SGPP1, SPPASE1"	Sphingosine-1-phosphate phosphatase 1	SGPP1	81537	ENSG00000126821			Sgpp1 (MGI:2135760)			
chr14	63761903	64226448	14q23	14q23.2		608442	"SYNE2, NUANCE, KIAA1011, EDMD5"	Spectrin repeat-containing nuclear envelope protein 2 (nesprin 2)	SYNE2	23224	ENSG00000054654		"Emery-Dreifuss muscular dystrophy 5, autosomal dominant, 612999 (3), Autosomal dominant"	Syne2 (MGI:2449316)			
chr14	64226711	64338630	14q	14q23.2-q23.3		601663	ESR2	Estrogen receptor-2 (ER beta)	ESR2	2100	ENSG00000140009			Esr2 (MGI:109392)			
chr14	64388040	64460006	14q24	14q23.3		172460	"MTHFD1, MTHFC, CIMAH"	Methylenetetrahydrofolate dehydrogenase 1	MTHFD1	4522	ENSG00000100714	trifunctional protein	"Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia, 617780 (3), Autosomal recessive; {Neural tube defects, folate-sensitive, susceptibility to}, 601634 (3), Autosomal recessive"	Mthfd1 (MGI:1342005)			
chr14	64449105	64505212	14q23-q24	14q23.3		194541	"ZBTB25, ZNF46, KUP"	Zinc finger and BTB domain containing 25	ZBTB25	7597	ENSG00000089775			Zbtb25 (MGI:99197)			
chr14	64465498	64474502	14q23.3	14q23.3		604688	"AKAP5, AKAP79"	A-kinase anchor protein 5	AKAP5	9495	ENSG00000179841			Akap5 (MGI:2685104)			
chr14	64504573	64533689	14q23.3	14q23.3		616578	ZBTB1	Zinc finger- and BTB domain-containing protein 1	ZBTB1	22890	ENSG00000126804			Zbtb1 (MGI:2442326)			
chr14	64540467	64543236	14q24.1	14q23.3		140560	HSPA2	Heat-shock 70kD protein-2	HSPA2	3306	ENSG00000126803			Hspa2 (MGI:96243)			
chr14	64744105	64879888	14q23.3	14q23.3		182870	"SPTB, SPH2, EL3, HS2"	"Spectrin, beta, erythrocytic"	SPTB	6710	ENSG00000070182		"Anemia, neonatal hemolytic, fatal and near-fatal (3); Elliptocytosis-3 (3); Spherocytosis, type 2, 616649 (3), Autosomal dominant"	Sptb (MGI:98387)			
chr14	64914360	64935367	14q23.3	14q23.3		608577	"CHURC1, CHCH, C14orf52"	Churchill domain-containing 1	CHURC1	91612	ENSG00000258289			Churc1 (MGI:1923684)			
chr14	64939151	64942904	14q24.1	14q23.3		138319	GPX2	"Glutathione peroxidase-2, gastrointestinal"	GPX2	2877	ENSG00000176153			Gpx2 (MGI:106609)			
chr14	64986788	65062651	14q23-q24	14q23.3		134636	FNTB	"Farnesyltransferase, CAAX box, beta"	FNTB	2342	ENSG00000257365	related FNTBL1 on 9		Fntb (MGI:1861305)			
chr14	65006100	65102694	14q23	14q23.3		154950	MAX	MAX protein	MAX	4149	ENSG00000125952	interacts with MYC	"{Pheochromocytoma, susceptibility to}, 171300 (3), Autosomal dominant"	Max (MGI:96921)			
chr14	65410591	65744121	14q23	14q23.3		602589	FUT8	Fucosyltransferase 8	FUT8	2530	ENSG00000033170			Fut8 (MGI:1858901)			
chr14	66507406	67735830	14q24	14q23.3-q24.1		603930	"GPHN, GPH, KIAA1385, GEPH, MOCODC"	Gephyrin	GPHN	10243	ENSG00000171723		"Molybdenum cofactor deficiency C, 615501 (3), Autosomal recessive"	Gphn (MGI:109602)			
chr14	67241294	67336060	14q23.3	14q23.3		606958	"MPP5, PALS1"	"Membrane protein, palmitoylated 5"	MPP5	64398	ENSG00000072415			Mpp5 (MGI:1927339)			
chr14	67337863	67360002	14q24	14q23.3		609398	"ATP6V1D, ATP6M"	"ATPase, H+ transporting, lysosomal, 34-kD, V1 subunit D"	ATP6V1D	51382	ENSG00000100554			Atp6v1d (MGI:1921084)			
chr14	67386978	67412199	14q23.3	14q23.3-q24.1		608007	PLEK2	Pleckstrin 2	PLEK2	26499	ENSG00000100558			Plek2 (MGI:1351466)			
chr14	67589305	67600301	14q11-q24	14q24.1		600154	PIGH	"Phosphatidylinositol glycan, class H"	PIGH	5283	ENSG00000100564			Pigh (MGI:99463)			
chr14	67619861	67651719	14q24.1-q24.3	14q24.1		107830	ARG2	Arginase II	ARG2	384	ENSG00000081181			Arg2 (MGI:1330806)			
chr14	67651148	67674884	14q24.1	14q24.1		603207	"VTI1B, VTI1, VTI1L"	"Vti1, S. cerevisiae, homolog of, B"	VTI1B	10490	ENSG00000100568			Vti1b (MGI:1855688)			
chr14	67676799	67695792	14q23.3	14q24.1		607849	"RDH11, PSDR1, RALR1, RDJCSS"	Retinol dehydrogenase 11	RDH11	51109	ENSG00000072042	mutation identified in 1 RDJCSS family	"?Retinal dystrophy, juvenile cataracts, and short stature syndrome, 616108 (3), Autosomal recessive"	Rdh11 (MGI:102581)			
chr14	67701885	67734450	14q23.3	14q24.1		608830	"RDH12, LCA13"	Retinol dehydrogenase 12	RDH12	145226	ENSG00000139988	near RDH11	"Leber congenital amaurosis 13, 612712 (3), Autosomal recessive"	Rdh12 (MGI:1925224)			
chr14	67728891	67817292	14q24.1	14q24.1		612012	"ZFYVE26, KIAA0321, SPG15"	Zinc finger FYVE domain-containing protein 26	ZFYVE26	23503	ENSG00000072121		"Spastic paraplegia 15, autosomal recessive, 270700 (3), Autosomal recessive"	Zfyve26 (MGI:1924767)			
chr14	67819778	68683117	14q23.3-q24	14q24.1		602948	RAD51L1	"RAD51. S. cerevisiae, homolog of, like 1"	RAD51B	5890	ENSG00000182185	fused with HMGA2 in uterine leiomyoma		Rad51b (MGI:1099436)			
chr14	68787654	68796242	14q22-q24	14q24.1		601064	"ZFP36L1, BRF1, ERF1"	"Zinc finger protein 36, C3H type-like 1 (butyrate response factor 1; EGF-response factor 1)"	ZFP36L1	677	ENSG00000185650			Zfp36l1 (MGI:107946)			
chr14	68874122	68979365	14q24.1	14q24.1		102575	"ACTN1, BDPLT15"	"Actinin, alpha-1"	ACTN1	87	ENSG00000072110		"Bleeding disorder, platelet-type, 15, 615193 (3), Autosomal dominant"	Actn1 (MGI:2137706)			
chr14	69050919	69153392	14q24.1-q24.2	14q24.1		603812	"DCAF5, WDR22, BCRP2, D14S1461E"	DDB1- and CUL4-associated factor 5	DCAF5	8816	ENSG00000139990			Dcaf5 (MGI:2444785)			
chr14	69191476	69244019	14q24.1	14q24.1		616940	"EXD2, EXDL2"	Exonuclease 3'-to-5' domain-containing protein 2	EXD2	55218	ENSG00000081177			Exd2 (MGI:1922485)			
chr14	69259545	69379903	14q24.1	14q24.1		615132	"GALNT16, GALNACT16, GALNTL1, KIAA1130"	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 16	GALNT16	57452	ENSG00000100626			Galnt16 (MGI:1917754)			
chr14	69380122	69398303	14q24.1	14q24.1		601191	ERH	"Enhancer of rudimentary, Drosophila, homolog of"	ERH	2079	ENSG00000100632	possible pseudogene on 7q34		Erh (MGI:108089)			
chr14	69611592	69715143	14q24.1	14q24.1		616761	"SUSD6, DRAGO, KIAA0247"	SUSHI domain-containing protein 6	SUSD6	9766	ENSG00000100647			Susd6 (MGI:2444661)			
chr14	69767086	69772004	14q24.2	14q24.1		600914	"SRSF5, SFRS5, SRp40"	"Splicing factor, serine/arginine-rich, 5"	SRSF5	6430	ENSG00000100650						
chr14	69775834	69797288	14q24.1	14q24.1		182396	"SLC10A1, NTCP1"	"Solute carrier family 10 (sodium/bile acid cotransporter family), member 1"	SLC10A1	6554	ENSG00000100652			Slc10a1 (MGI:97379)			
chr14	69879387	70032365	14q24.1	14q24.2		608488	"SMOC1, OAS"	SPARC-related modular calcium-binding 1	SMOC1	64093	ENSG00000198732		"Microphthalmia with limb anomalies, 206920 (3), Autosomal recessive"	Smoc1 (MGI:1929878)			
chr14	70366495	70417089	14q24.2	14q24.2		609411	"SYNJ2BP, OMP25, ARIP2"	Synaptojanin 2-binding protein	SYNJ2BP	55333	ENSG00000213463			Synj2bp (MGI:1344347)			
chr14	70452156	70459904	14q24.1	14q24.2		603713	ADAM21	A disintegrin and metalloproteinase domain 21	ADAM21	8747	ENSG00000139985			Adam21 (MGI:1861229)			
chr14	70520816	70564741	14q24.1	14q24.2		603712	ADAM20	A disintegrin and metalloproteinase domain 20	ADAM20	8748	ENSG00000134007			"Adam20,Adam25,Adam39 (MGI:3045694,MGI:1345157,MGI:2152342)"			
chr14	70641786	70675359	14q24.2	14q24.2		610488	"TTC9, KIAA0227"	Tetratricopeptide repeat domain-containing protein 9	TTC9	23508	ENSG00000133985			Ttc9 (MGI:1916730)			
chr14	70722525	70809261	14q24.3-q31	14q24.2		600136	"MAP3K9, MLK1"	Mitogen-activated protein kinase kinase kinase 9	MAP3K9	4293	ENSG00000006432			Map3k9 (MGI:2449952)			
chr14	70907404	71115381	14q24.2	14q24.2		617655	"PCNX1, KIAA0995"	"Pecanex, Drosophila, homolog of, 1"	PCNX1	22990	ENSG00000100731			Pcnx (MGI:1891924)			
chr14	71320417	71741228	14q24.2	14q24.2		617504	"SIPA1L1, E6TP1, KIAA0440"	SIPA1-like protein 1	SIPA1L1	26037	ENSG00000197555			Sipa1l1 (MGI:2443679)			
chr14	71867396	72632477	14q24.3	14q24.2		603894	RGS6	Regulator of G protein signaling 6	RGS6	9628	ENSG00000182732			Rgs6 (MGI:1354730)			
chr14	72609031	72894115	14q24.3-q31.1	14q24.2		601672	"DPF3, CERD4"	"D4, zinc and double PHD fingers, family 3"	DPF3	8110	ENSG00000205683			Dpf3 (MGI:1917377)			
chr14	72926331	72962097	14q24.2	14q24.2		616372	"DCAF4, WDR21, WDR21A"	DDB1- and CUL4-associated factor 4	DCAF4	26094	ENSG00000119599			Dcaf4 (MGI:1921078)			
chr14	72969444	73027211	14q22-q24	14q24.2		605471	"ZFYVE1, ZNFN2A1, DFCP1, TAFF1"	Zinc finger FYVE type-containing protein 1	ZFYVE1	53349	ENSG00000165861			Zfyve1 (MGI:3026685)			
chr14	73058512	73121413	14q24.2	14q24.2		612427	"RBM25, RED120"	RNA-binding motif protein 25	RBM25	58517	ENSG00000119707						
chr14	73136434	73223690	14q24.3	14q24.2		104311	"PSEN1, AD3, ACNINV3"	Presenilin 1	PSEN1	5663	ENSG00000080815	mutation identified in 1 ACNINV3 family	"?Acne inversa, familial, 3, 613737 (3), Autosomal dominant; Alzheimer disease, type 3, 607822 (3), Autosomal dominant; Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822 (3), Autosomal dominant; Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822 (3), Autosomal dominant; Cardiomyopathy, dilated, 1U, 613694 (3), Autosomal dominant; Dementia, frontotemporal, 600274 (3), Autosomal dominant; Pick disease, 172700 (3), Autosomal dominant, Isolated cases"	Psen1 (MGI:1202717)			
chr14	73235840	73274639	14q24.2	14q24.2		617785	"PAPLN, PPN"	"Papilin, proteoglycan-like sulfated glycoprotein"	PAPLN	89932	ENSG00000100767			Papln (MGI:2386139)			
chr14	73275209	73458579	14q24.3	14q24.2-q24.3		603728	"NUMB, S171"	"Numb, Drosophila, homolog of"	NUMB	8650	ENSG00000133961			Numb (MGI:107423)			
chr14	73300000	78800000	14q24.3			613085	GLC3C	"Glaucoma 3, primary congenital, C"	GLC3C	399565		between D14S61 and D14S1000	"Glaucoma 3, primary congenital, C, 613085 (2)"				
chr14	73300000	89300000	14q24.3-q31			601208	IDDM11	Insulin-dependent diabetes mellitus-11	IDDM11	3410			"{Diabetes mellitus, insulin-dependent, 11}, 601208 (2)"				
chr14	73300000	78800000	14q24.3			614628	KTCN8	Keratoconus 8		100885803		between rs1074501 and rs755212	"Keratoconus 8, 614628 (2), Autosomal dominant"				
chr14	73300000	78800000	14q24.3			612083	MUSTQTL1	Muscle strength quantitative trait locus 1		100192311			"Muscle strength quantitative trait locus 1, 612083 (2)"				
chr14	73490933	73493400	14q24.3	14q24.3		611919	"RIOX1, C14orf169, NO66, MAPJD"	Ribosomal oxygenase 1	RIOX1	79697	ENSG00000170468			Riox1 (MGI:1919202)			
chr14	73493020	73543798	14q24.3	14q24.3		614313	ACOT1	Acyl-CoA thioesterase 1	ACOT1	641371	ENSG00000184227			Acot3 (MGI:2159619)			
chr14	73567619	73575657	14q24.3	14q24.3		609972	"ACOT2, PTE2, MTE1"	Acyl-CoA thioesterase 2	ACOT2	10965	ENSG00000119673			Acot2 (MGI:2159605)			
chr14	73591705	73595765	14q24.3	14q24.3		614314	ACOT4	Acyl-CoA thioesterase 4	ACOT4	122970	ENSG00000177465	?pseudogene on 19q13.12		Acot4 (MGI:2159621)			
chr14	73612275	73619928	14q24.3	14q24.3		614267	ACOT6	Acyl-CoA thioesterase 6	ACOT6	641372	ENSG00000205669						
chr14	73644874	73703727	14q24.3	14q24.3		610062	"DNAL1, C14orf168, CILD16"	"Dynein, axonemal, light chain 1"	DNAL1	83544	ENSG00000119661		"Ciliary dyskinesia, primary, 16, 614017 (3), Autosomal recessive"	Dnal1 (MGI:1921462)			
chr14	73711782	73714424	14q24.3	14q24.3		604010	"PNMA1, MA1"	Paraneoplastic MA antigen 1	PNMA1	9240	ENSG00000176903			Pnma1 (MGI:2180564)			
chr14	73851830	73885464	14q24	14q24.3		608642	ZADH1	Zinc-binding alcohol dehydrogenase domain-containing protein 1	PTGR2	145482	ENSG00000140043			Ptgr2 (MGI:1916372)			
chr14	73949933	73963459	14q24.3	14q24.3		614647	"COQ6, CGI10, COQ10D6"	"Coq6, S. cerevisiae, homolog of"	COQ6	51004	ENSG00000119723		"Coenzyme Q10 deficiency, primary, 6, 614650 (3), Autosomal recessive"	Coq6 (MGI:1924408)			
chr14	73957915	74019331	14q24	14q24.3		603162	"ENTPD5, CD39L4"	Ectonucleoside triphosphate diphosphohydrolase 5	ENTPD5	957	ENSG00000187097			Entpd5 (MGI:1321385)			
chr14	74057661	74084492	14q24.3	14q24.3		603178	"ALDH6A1, MMSDH"	"Aldehyde dehydrogenase 6 family, member A1 (methylmalonate semialdehyde dehydrogenase)"	ALDH6A1	4329	ENSG00000119711		"Methylmalonate semialdehyde dehydrogenase deficiency, 614105 (3), Autosomal recessive"	Aldh6a1 (MGI:1915077)			
chr14	74239471	74262737	14q24.3	14q24.3		142993	"CHX10, HOX10, MCOP2, MCOPCB3"	C. elegans ceh-10 homeo domain-containing homolog	VSX2	338917	ENSG00000119614		"Microphthalmia with coloboma 3, 610092 (3); Microphthalmia, isolated 2, 610093 (3)"	Vsx2 (MGI:88401)			
chr14	74285276	74303063	14q24.3	14q24.3		603214	"ABCD4, PXMP1L, P79R, PMP69, MAHCJ"	"ATP-binding cassette, subfamily D, member 4 (peroxisomal membrane protein 1-like)"	ABCD4	5826	ENSG00000119688		"Methylmalonic aciduria and homocystinuria, cblJ type, 614857 (3), Autosomal recessive"	Abcd4 (MGI:1349217)			
chr14	74405892	74477079	14q24.3	14q24.3		609999	"SYNDIG1L, TMEM90A, CAPUCIN"	Synapse differentiation-induced gene 1-like	SYNDIG1L	646658	ENSG00000183379			Syndig1l (MGI:2685107)			
chr14	74479939	74493380	14q24.3	14q24.3		601015	"NPC2, HE1"	Epididymal secretory protein HE1	NPC2	10577	ENSG00000119655		"Niemann-pick disease, type C2, 607625 (3), Autosomal recessive"	Npc2 (MGI:1915213)			
chr14	74493719	74495567	14q24.3	14q24.3		615317	"ISCA2, MMDS4"	"Iron-sulfur cluster assembly 2, S. cerevisiae, homolog of"	ISCA2	122961	ENSG00000165898		"Multiple mitochondrial dysfunctions syndrome 4, 616370 (3), Autosomal recessive"	Isca2 (MGI:1921566)			
chr14	74498182	74612592	14q24	14q24.3		602091	"LTBP2, LTBP3, GLC3D, MSPKA, WMS3"	Latent transforming growth factor beta binding protein-2	LTBP2	4053	ENSG00000119681	mutation identified in 1 WMS3 family	"Glaucoma 3, primary congenital, D, 613086 (3); Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, 251750 (3), Autosomal recessive; ?Weill-Marchesani syndrome 3, recessive, 614819 (3), Autosomal recessive"	Ltbp2 (MGI:99502)			
chr14	74661251	74713117	14q24.3	14q24.3		615380	"AREL1, KIAA0317"	Apoptosis-resistant E3 ubiquitin protein ligase 1	AREL1	9870	ENSG00000119682			Arel1 (MGI:1915747)			
chr14	74853032	74876662	14q24.3	14q24.3		615094	PROX2	Prospero-related homeobox 2	PROX2	283571	ENSG00000119608			Prox2 (MGI:1920672)			
chr14	74881890	74903746	14q24.3	14q24.3		126063	DLST	Dihydrolipoamide S-succinyltransferase (E2 component of 2-oxo-glutarate complex)	DLST	1743	ENSG00000119689			Dlst (MGI:1926170)			
chr14	74941829	74955763	14q24-q31	14q24.3		601121	"PGF, PLGF"	"Placental growth factor, vascular endothelial growth factor-related protein"	PGF	5228	ENSG00000119630			Pgf (MGI:105095)			
chr14	75002908	75009590	14q24	14q24.3		606454	EIF2B2	"Eukaryotic translation initiation factor 2B, subunit 2"	EIF2B2	8892	ENSG00000119718		"Leukoencephalopathy with vanishing white matter, 603896 (3), Autosomal recessive; Ovarioleukodystrophy, 603896 (3), Autosomal recessive"	Eif2b2 (MGI:2145118)			
chr14	75013763	75051531	14q24.3	14q24.3		604395	"MLH3, HNPCC7"	Mismatch repair gene MLH3	MLH3	27030	ENSG00000119684		"Colorectal cancer, hereditary nonpolyposis, type 7, 614385 (3); Colorectal cancer, somatic, 114500 (3); {Endometrial cancer, susceptibility to}, 608089 (3)"	Mlh3 (MGI:1353455)			
chr14	75053220	75069482	14q24.3	14q24.3		600875	"ACYP1, ACYPE"	"Acylphosphatase, erythrocyte"	ACYP1	97	ENSG00000119640			Acyp1 (MGI:1913454)			
chr14	75081378	75127636	14q24.3	14q24.3		609798	"NEK9, NERCC1, LCCS10, APUG, NC"	Never in mitosis gene A-related kinase 9	NEK9	91754	ENSG00000119638	mutation identified in 1 APUG family	"?Arthrogryposis, Perthes disease, and upward gaze palsy, 614262 (3), Autosomal recessive; Lethal congenital contracture syndrome 10, 617022 (3), Autosomal recessive; Nevus comedonicus, somatic, 617025 (3)"	Nek9 (MGI:2387995)			
chr14	75131467	75176645	14q24.3	14q24.3		605406	"TMED10, TMP21"	Transmembrane p24 trafficking protein 10	TMED10	10972	ENSG00000170348			"Tmed10,Tmed10-ps (MGI:3782198,MGI:1915831)"			
chr14	75278777	75282233	14q24.3	14q24.3		164810	FOS	FBJ murine osteosarcoma viral (v-fos) oncogene homolog (oncogene FOS)	FOS	2353	ENSG00000170345			Fos (MGI:95574)			
chr14	75426691	75472700	14q24.3	14q24.3		608657	JDP2	JUN dimerization protein 2	JDP2	122953	ENSG00000140044			Jdp2 (MGI:1932093)			
chr14	75522440	75546991	14q24	14q24.3		612476	"BATF, BATF1, SFA2"	"Basic leucine zipper transcription factor, ATF-like"	BATF	10538	ENSG00000156127			Batf (MGI:1859147)			
chr14	75578596	75648168	14q24.3	14q24.3		610865	"FLVCR2, C14orf58, CCT, PVHH, EPV"	Feline leukemia virus subgroup C receptor 2	FLVCR2	55640	ENSG00000119686		"Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, 225790 (3), Autosomal recessive"	Flvcr2 (MGI:2384974)			
chr14	75650889	75661194	14q24	14q24.3		604576	"ERG28, C14orf1"	Ergosterol biosynthesis 28 homolog	ERG28	11161	ENSG00000133935			Erg28 (MGI:1915571)			
chr14	75661207	75955081	14q24.3	14q24.3		612268	"TTLL5, STAMP, KIAA0998, CORD19"	"Tubulin tyrosine ligase-like family, member 5"	TTLL5	23093	ENSG00000119685		"Cone-rod dystrophy 19, 615860 (3), Autosomal recessive"	Ttll5 (MGI:2443657)			
chr14	75958060	75983010	14q24	14q24.3		190230	"TGFB3, ARVD1, RNHF, LDS5"	"Transforming growth factor, beta-3"	TGFB3	7043	ENSG00000119699		"Arrhythmogenic right ventricular dysplasia 1, 107970 (3), Autosomal dominant; Loeys-Dietz syndrome 5, 615582 (3), Autosomal dominant"	Tgfb3 (MGI:98727)			
chr14	75985752	76084072	14q24.3	14q24.3		614068	"IFT43, C14orf179, CED3, SRTD18, RP81"	"Intraflagellar transport 43, Chlamydomonas, homolog of"	IFT43	112752	ENSG00000119650	mutation identified in 1 CED3 family and 1 RP81 family	"?Cranioectodermal dysplasia 3, 614099 (3), Autosomal recessive; ?Retinitis pigmentosa 81, 617871 (3), Autosomal recessive; Short-rib thoracic dysplasia 18 with polydactyly, 617866 (3), Autosomal recessive"	Ift43 (MGI:1923661)			
chr14	76371346	76501838	14q24.3	14q24.3		602167	"ESRRB, ESRL2, DFNB35"	Estrogen-related receptor beta	ESRRB	2103	ENSG00000119715		"Deafness, autosomal recessive 35, 608565 (3), Autosomal recessive"	Esrrb (MGI:1346832)			
chr14	77024542	77028698	14q24.3	14q24.3		611720	"IRF2BPL, C14orf4, EAP1"	Interferon regulatory factor 2-binding protein like	IRF2BPL	64207	ENSG00000119669			Irf2bpl (MGI:2442463)			
chr14	77098234	77117286	14q24.3	14q24.3		616995	"CIPC, KIAA1737"	Clock-interacting pacemaker	CIPC	85457	ENSG00000198894			Cipc (MGI:1919185)			
chr14	77265490	77271311	14q24	14q24.3		605304	NGB	Neuroglobin	NGB	58157	ENSG00000165553			Ngb (MGI:2151886)			
chr14	77274955	77320884	14q24.3	14q24.3		607439	"POMT2, MDDGA2, MDDGB2, MDDGC2"	Putative protein O-mannosyltransferase 2	POMT2	29954	ENSG00000009830		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2, 613156 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2, 613158 (3), Autosomal recessive"	Pomt2 (MGI:2444430)			
chr14	77320886	77331596	14q24.3	14q24.3		603758	"GSTZ1, MAAI, MAAID"	"Glutathione S-transferase, zeta-1 (maleylacetoacetate isomerase)"	GSTZ1	2954	ENSG00000100577		"[Maleylacetoacetate isomerase deficiency], 617596 (3), Autosomal recessive"	Gstz1 (MGI:1341859)			
chr14	77426674	77457726	14q24.3	14q24.3		613401	"VIPAS39, VIPAR, SPE39, C14orf133"	"VPS33B-interacting protein, apical-basolateral polarity regulator, spe-39 homolog"	VIPAS39	63894	ENSG00000151445		"Arthrogryposis, renal dysfunction, and cholestasis 2, 613404 (3), Autosomal recessive"	Vipas39 (MGI:2144805)			
chr14	77457876	77469471	14q24.3	14q24.3		608466	"AHSA1, AHA1"	Activator of heat-shock 90kD protein ATPase 1	AHSA1	10598	ENSG00000100591			Ahsa1 (MGI:2387603)			
chr14	77474393	77498866	14q24.3	14q24.3		612684	"ISM2, THSD3, TAIL1"	"Isthmin 2, zebrafish, homolog of"	ISM2	145501	ENSG00000100593						
chr14	77505996	77616766	14q24.3-q31	14q24.3		605713	"SPTLC2, KIAA0526, SPT2, LCB2, HSN1C, NSAN1C"	"Serine palmitoyltransferase, long-chain base subunit 2"	SPTLC2	9517	ENSG00000100596		"Neuropathy, hereditary sensory and autonomic, type IC, 613640 (3), Autosomal dominant"	Sptlc2 (MGI:108074)			
chr14	77672403	77708037	14q24	14q24.3		605345	"ALKBH1, ALKB"	"AlkB, E. coli, homolog of, 1"	ALKBH1	8846	ENSG00000100601			Alkbh1 (MGI:2384034)			
chr14	77708070	77717597	14q24.3	14q24.3		610211	"SLIRP, C14orf156"	SRA stem loop-interacting RNA-binding protein	SLIRP	81892	ENSG00000119705			Slirp (MGI:1916394)			
chr14	77717598	77761155	14q24.3	14q24.3		603055	"SKIIP, SKIP, SNW1, BX42"	SKI-interacting protein	SNW1	22938	ENSG00000100603			Snw1 (MGI:1913604)			
chr14	77979903	79868289	14q24.3-q31.1	14q24.3-q31.1		600567	NRXN3	Neurexin 3	NRXN3	9369	ENSG00000021645						
chr14	78800000	89300000	14q31			275000	GRD1	"Graves disease, susceptibility to, 1"		100312954		associated with rs2268458	"{Graves disease, susceptibility to, 1}, 275000 (2), Autosomal recessive"				
chr14	78800000	89300000	14q31			614187	HPPD	"Hypertelorism, preauricular sinus, punctal pits, and deafness"		100682260			"Hypertelorism, preauricular sinus, punctal pits, and deafness, 614187 (2), Autosomal dominant"				
chr14	80197524	80231053	14q24.3	14q31.1		601413	"DIO2, TXDI2, D2"	"Deiodinase, iodothyronine, type II"	DIO2	1734	ENSG00000211448			Dio2 (MGI:1338833)			
chr14	80954988	81146301	14q31	14q31.1		603372	"TSHR, CHNG1"	Thyroid-stimulating hormone receptor	TSHR	7253	ENSG00000165409		"Hyperthyroidism, familial gestational, 603373 (3); Hyperthyroidism, nonautoimmune, 609152 (3), Autosomal dominant, Isolated cases; Hypothyroidism, congenital, nongoitrous, 1, 275200 (3), Autosomal recessive; Thyroid adenoma, hyperfunctioning, somatic (3); Thyroid carcinoma with thyrotoxicosis (3)"	Tshr (MGI:98849)			
chr14	81175451	81221230	14q31.1	14q31.1		600520	"GTF2A1, TF2A1"	"General transcription factor IIA, alpha/beta subunits"	GTF2A1	2957	ENSG00000165417			Gtf2a1 (MGI:1933277)			
chr14	81260649	81436463	14q13.1	14q31.1		608467	"STON2, STN2, STNB"	Stonin 2	STON2	85439	ENSG00000140022			Ston2 (MGI:1918272)			
chr14	81471546	81533860	14q31	14q31.1		602329	SEL1L	"Suppressor of lin 12 (sel-1), C. elegans, homolog of"	SEL1L	6400	ENSG00000071537			Sel1l (MGI:1329016)			
chr14	85527371	85628695	14q24-q32	14q31.3		604807	FLRT2	Fibronectin-like domain-containing leucine-rich transmembrane protein-2	FLRT2	23768	ENSG00000185070			Flrt2 (MGI:3603594)			
chr14	87933013	87993664	14q31	14q31.3		606890	GALC	Galactosylceramidase	GALC	2581	ENSG00000054983		"Krabbe disease, 245200 (3), Autosomal recessive"	Galc (MGI:95636)			
chr14	88005123	88014810	14q31-q32.1	14q31.3		604620	"GPR65, TDAG8"	G protein-coupled receptor 65	GPR65	8477	ENSG00000140030			Gpr65 (MGI:108031)			
chr14	88180107	88326911	14q31	14q31.3		605873	"KCNK10, TREK2"	"Potassium channel, subfamily K, member 10"	KCNK10	54207	ENSG00000100433			Kcnk10 (MGI:1919508)			
chr14	88385637	88470349	14q31.3	14q31.3		609868	"SPATA7, HSD3, LCA3"	Spermatogenesis-associated protein 7	SPATA7	55812	ENSG00000042317		"Leber congenital amaurosis 3, 604232 (3); Retinitis pigmentosa, juvenile, autosomal recessive, 604232 (3)"	Spata7 (MGI:2144877)			
chr14	88465777	88554778	14q31.3	14q31.3		603271	"PTPN21, PTPD1"	"Protein-tyrosine phosphatase, nonreceptor-type, 21"	PTPN21	11099	ENSG00000070778			Ptpn21 (MGI:1344406)			
chr14	88562908	88613508	14q31.3	14q31.3		613279	"ZC3H14, SUT2, MRT56"	Zinc finger CCCH domain-containing protein 14	ZC3H14	79882	ENSG00000100722		"Mental retardation, autosomal recessive 56, 617125 (3), Autosomal recessive"	Zc3h14 (MGI:1919824)			
chr14	88824152	88877995	14q32.1	14q31.3		608132	"TTC8, BBS8, RP51"	Tetratricopeptide repeat domain 8	TTC8	123016	ENSG00000165533	mutation identified in 1 RP51 family	"Bardet-Biedl syndrome 8, 615985 (3), Autosomal recessive; ?Retinitis pigmentosa 51, 613464 (3), Autosomal recessive"	Ttc8 (MGI:1923510)			
chr14	89156171	89619149	14q24.3-q31	14q31.3-q32.1		602628	"FOXN3, CHES1"	Forkhead box N3	FOXN3	1112	ENSG00000053254						
chr14	89300000	107043718	14q32			608318	CHDS4	"Coronary heart disease, susceptibility to, 4"		387585		highest LOD with D14S1426	"{Coronary heart disease, susceptibility to, 4}, 608318 (2)"				
chr14	89300000	107043718	14q32			123270	CKBE	"Creatine kinase, ectopic expression"	CKBE	1156		"linked to IGH, PI; ?same locus as CKBB"	"[Creatine kinase, brain type, ectopic expression of], 123270 (2)"				
chr14	89300000	107043718	14q32			616604	"DUP14q32, C14DUPq32"	"Chromosome 14q32 duplication syndrome, 700kB"				heterozygous germline duplication of 700kb	"{Myeloproliferative neoplasms, familial, susceptibility to}, 616604 (4), Autosomal dominant"				
chr14	89300000	107043718	14q32			608875	GEVQ1	"Gene expression, variation in, quantitative trait locus on chromosome 14"		474334			"{Gene expression, variation in, QTL}, 608875 (2)"				
chr14	89300000	107043718	14q32			164210	HFM	Hemifacial microsomia		170474			"Hemifacial microsomia, 164210 (2), Autosomal dominant"				
chr14	89300000	107043718	14q32			608149	KAOGS	Kagami-Ogata syndrome				uniparental isodisomy of imprinted region of chromosome 14	"Kagami-Ogata syndrome, 608149 (4), Isolated cases"				
chr14	89300000	107043718	14q32			251600	MCOP1	"Microphthalmia, isolated 1"		8113			"Microphthalmia, isolated 1, 251600 (2), Autosomal recessive"				
chr14	89300000	95800000	14q32.1			107410	"SERPINA2P, PIL, ATR, ARGS"	"Serpin peptidase inhibitor, clade A, member 2, pseudogene"	SERPINA2	390502	ENSG00000258597	?pseudogene					
chr14	89300000	107043718	14q32			616222	TEMPS	Temple syndrome (maternal uniparental disomy chromosome 14)					"Temple syndrome, 616222 (4), Isolated cases"				
chr14	89954922	90044767	14q31-q32	14q32.11		607198	TDP1	Tyrosyl-DNA phosphodiesterase 1	TDP1	55775	ENSG00000042088		"Spinocerebellar ataxia, autosomal recessive with axonal neuropathy, 607250 (3)"	Tdp1 (MGI:1920036)			
chr14	90061764	90185856	14q24.1-q24.3	14q32.11		607367	"KCNK13, THIK1"	"Potassium channel, subfamily K, member 13"	KCNK13	56659	ENSG00000152315			Kcnk13 (MGI:2384976)			
chr14	90256549	90272624	14q32.11	14q32.11		602706	"PSMC1, S4"	"Proteasome 26S subunit, ATPase, 1"	PSMC1	5700	ENSG00000100764	previously assigned to 19p13.3 by FISH		Psmc1 (MGI:106054)			
chr14	90396982	90408274	14q24-q31	14q32.11		114180	"CALM1, PHKD, CPVT4, LQT14"	"Calmodulin-1 (phosphorylase kinase, delta)"	CALM1	801	ENSG00000198668		"Long QT syndrome 14, 616247 (3), Autosomal dominant; Ventricular tachycardia, catecholaminergic polymorphic, 4, 614916 (3), Autosomal dominant"				
chr14	90868121	91060648	14q31-q32	14q32.11		603607	"RPS6KA5, MSK1"	"Ribosomal protein S6 kinase, 90kD, 5"	RPS6KA5	9252	ENSG00000100784			Rps6ka5 (MGI:1920336)			
chr14	91232531	91264580	14q31	14q32.11		601404	"GPR68, OGR1, AI2A6"	G protein-coupled receptor 68	GPR68	8111	ENSG00000119714		"Amelogenesis imperfecta, hypomaturation type, IIA6, 617217 (3), Autosomal recessive"	Gpr68 (MGI:2441763)			
chr14	91271322	91417843	14q32.11	14q32.11-q32.12		611204	"CCDC88C, HKRP2, DAPLE, KIAA1509, HYC, SCA40"	Coiled-coil domain-containing protein 88C	CCDC88C	440193	ENSG00000015133	mutation identified in 1 SCA40 family	"Hydrocephalus, nonsyndromic, autosomal recessive, 236600 (3), Autosomal recessive; ?Spinocerebellar ataxia 40, 616053 (3), Autosomal dominant"	Ccdc88c (MGI:1915589)			
chr14	91457480	91510553	14q32.12	14q32.12		610351	"PPP4R3A, SMEK1, PP4R3A, KIAA2010"	"Protein phosphatase 4, regulatory subunit 3, alpha"	PPP4R3A	55671	ENSG00000100796			Ppp4r3a (MGI:1915984)			
chr14	91580773	91732085	14q32.12	14q32.12		611169	"CATSPERB, C14orf161"	"Cation channel, sperm-associated, beta"	CATSPERB	79820	ENSG00000133962			Catsperb (MGI:2443988)			
chr14	91869410	91947701	14q32.1	14q32.12		604580	"FBLN5, ARMD3, ADCL2, ARCL1A, HNARMD"	Fibulin 5	FBLN5	10516	ENSG00000140092		"Cutis laxa, autosomal dominant 2, 614434 (3); Cutis laxa, autosomal recessive, type IA, 219100 (3), Autosomal recessive; Macular degeneration, age-related, 3, 608895 (3), Autosomal dominant; Neuropathy, hereditary, with or without age-related macular degeneration, 608895 (3), Autosomal dominant"	Fbln5 (MGI:1346091)			
chr14	91965990	92040133	14q31-q32	14q32.12		604505	"TRIP11, TRIP230, CEV14, ACG1A"	Thyroid hormone receptor interactor 11	TRIP11	9321	ENSG00000100815		"Achondrogenesis, type IA, 200600 (3), Autosomal recessive"	Trip11 (MGI:1924393)			
chr14	92058551	92106620	14q32.12	14q32.12		607047	"ATXN3, MJD, SCA3"	Ataxin-3 (josephin)	ATXN3	4287	ENSG00000066427		"Machado-Joseph disease, 109150 (3), Autosomal dominant"	Atxn3 (MGI:1099442)			
chr14	92116122	92121808	14q32.12	14q32.12		603837	NDUFB1	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 1"	NDUFB1	4707	ENSG00000183648			Ndufb1-ps (MGI:3780865)			
chr14	92322580	92501480	14q32	14q32.12		609840	"SLC24A4, NCKX4, SHEP6, AI2A5"	"Solute carrier family 24 (sodium/potassium/calcium exchanger), member 4"	SLC24A4	123041	ENSG00000140090		"Amelogenesis imperfecta, type IIA5, 615887 (3), Autosomal recessive; [Skin/hair/eye pigmentation 6, blond/brown hair], 210750 (3), Autosomal recessive; [Skin/hair/eye pigmentation 6, blue/green eyes], 210750 (3), Autosomal recessive"	Slc24a4 (MGI:2447362)			
chr14	92703806	92748701	14q32.1	14q32.12		602620	"LGMN, PRSC1"	"Legumain (protease, cysteine, 1)"	LGMN	5641	ENSG00000100600			Lgmn (MGI:1330838)			
chr14	92794230	92839962	14q	14q32.12		606918	"GOLGA5, RFG5"	"Golgi autoantigen, golgin subfamily A, 5"	GOLGA5	9950	ENSG00000066455	fused with RET to form PTC5		Golga5 (MGI:1351475)			
chr14	92922593	92935292	14q32	14q32.12		118910	CHGA	"Chromogranin A, parathyroid secretory protein-1"	CHGA	1113	ENSG00000100604			Chga (MGI:88394)			
chr14	92936913	93115918	14q32.12	14q32.12		601838	"ITPK1, ITRPK1"	"Inositol 1,3,4-trisphosphate 5/6-kinase"	ITPK1	3705	ENSG00000100605			Itpk1 (MGI:2446159)			
chr14	93182195	93184903	14q32.12	14q32.12		609485	"MOAP1, MAP1, PNMA4"	Modulator of apoptosis 1	MOAP1	64112	ENSG00000165943			Moap1 (MGI:1915555)			
chr14	93202891	93207113	14q32.12	14q32.12		617436	"GON7, C14orf142"	"Gon7, S. cerevisiae, homolog of"	GON7	84520	ENSG00000170270			Gon7 (MGI:4845848)			
chr14	93207055	93229214	14q32.12	14q32.12		613816	UBR7	Ubiquitin protein ligase E3 component N-recognin 7	UBR7	55148	ENSG00000012963			Ubr7 (MGI:1913872)			
chr14	93237549	93333091	14q32.1	14q32.12		610386	"BTBD7, FUP1"	BTB/POX domain-containing protein 7	BTBD7	55727	ENSG00000011114			Btbd7 (MGI:1917858)			
chr14	93333218	93710472	14q32.12	14q32.12		616884	UNC79	"Unc79, C. elegans, homolog of"	UNC79	57578	ENSG00000133958			Unc79 (MGI:2684729)			
chr14	93347190	93348353	14q32.12	14q32.12		616855	COX8C	"Cytochrome c oxidase, subunit 8c"	COX8C	341947	ENSG00000187581						
chr14	93718297	93789028	14q32.12	14q32.12		613851	"PRIMA1, PRIMA"	Proline-rich membrane anchor 1	PRIMA1	145270	ENSG00000175785			Prima1 (MGI:1926097)			
chr14	93934152	93976738	14q32.12	14q32.12		605759	ASB2	Ankyrin repeat-containing SOCS box protein 2	ASB2	51676	ENSG00000100628			Asb2 (MGI:1929743)			
chr14	94015599	94048929	14q32.12	14q32.12		608338	"OTUB2, OTU2, OTB2, C14orf137"	OTU domain-containing ubiquitin aldehyde-binding protein 2	OTUB2	78990	ENSG00000089723			Otub2 (MGI:1915399)			
chr14	94050921	94081211	14q32	14q32.12		606181	DDX24	DEAD/H box 24	DDX24	57062	ENSG00000089737			Ddx24 (MGI:1351337)			
chr14	94110732	94116698	14q32	14q32.12		600009	IFI27	"Interferon, alpha-inducible protein-27"	IFI27	3429	ENSG00000165949						
chr14	94127780	94129619	14q32.12	14q32.12		611319	"IFI27L2, FAM14A, ISG12B"	Interferon alpha inducible protein 27 like 2	IFI27L2	83982	ENSG00000119632						
chr14	94174311	94279734	14q32.13	14q32.12-q32.13		616790	"PPP4R4, PP4R4, KIAA1622"	"Protein phosphatase 4, regulatory subunit 4"	PPP4R4	57718	ENSG00000119698			Ppp4r4 (MGI:1921771)			
chr14	94280459	94293352	14q32.1	14q32.13		605271	"SERPINA10, ZPI"	"Serine (or cysteine) proteinase inhibitor, clade A, member 10 (protein Z-dependent protease inhibitor precursor)"	SERPINA10	51156	ENSG00000140093			Serpina10 (MGI:2667725)			
chr14	94304247	94323350	14q32.1	14q32.13		122500	"CBG, SERPINA6"	Corticosteroid-binding globulin	SERPINA6	866	ENSG00000170099		"Corticosteroid-binding globulin deficiency, 611489 (3), Autosomal recessive, Autosomal dominant"	Serpina6 (MGI:88278)			
chr14	94376746	94390691	14q32.1	14q32.13		107400	"SERPINA1, PI, AAT"	"Alpha-1-antitrypsin (serpin peptidase inhibitor, clade A, member 1)"	SERPINA1	5265	ENSG00000197249		"Emphysema due to AAT deficiency, 613490 (3), Autosomal recessive; Emphysema-cirrhosis, due to AAT deficiency, 613490 (3), Autosomal recessive; Hemorrhagic diathesis due to antithrombin Pittsburgh, 613490 (3), Autosomal recessive; {Pulmonary disease, chronic obstructive, susceptibility to}, 606963 (1)"	"Serpina1e,Serpina1c,Serpina1d,Serpina1a,Serpina1b (MGI:891971,MGI:891970,MGI:891968,MGI:891969,MGI:891967)"			
chr14	94462720	94476332	14q32	14q32.13		615677	"SERPINA9, GCET1, CENTERIN"	"Serpin peptidase inhibitor, clade A, member 9"	SERPINA9	327657	ENSG00000170054			Serpina9 (MGI:1919157)			
chr14	94481650	94517843	14q32.1	14q32.13		617471	"SERPINA12, VASPIN"	"Serpin peptidase inhibitor, clade A, member 12 (vaspin)"	SERPINA12	145264	ENSG00000165953			Serpina12 (MGI:1915304)			
chr14	94561419	94569912	14q31-q32.1	14q32.13		147935	"SERPINA4, KST, PI4"	"Serpin peptidase inhibitor, clade A, member 4"	SERPINA4	5267	ENSG00000100665	"in cluster with related AAT, AACT, CBG, PCI"					
chr14	94581368	94593119	14q32.1	14q32.13		601841	"SERPNA5, PCI"	"Serpin peptidase inhibitor, clade A, member 5 (protein C inhibitor)"	SERPINA5	5104	ENSG00000188488			Serpina5 (MGI:107817)			
chr14	94612376	94624052	14q32.1	14q32.13		107280	"SERPINA3, AACT, ACT"	Alpha-1-antichymotrypsin	SERPINA3	12	ENSG00000196136	220kb from PI	"Alpha-1-antichymotrypsin deficiency (3); Cerebrovascular disease, occlusive (3)"	"Serpina3m,Serpina3n,Serpina3k,Serpina3c (MGI:98378,MGI:105045,MGI:102848,MGI:98377)"			
chr14	94768222	94770161	14q32.1	14q32.13		138890	"GSC, SAMS"	Goosecoid	GSC	145258	ENSG00000133937		"Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities, 602471 (3), Autosomal recessive"	Gsc (MGI:95841)			
chr14	95086227	95158262	14q31	14q32.13		606241	"DICER1, HERNA, KIAA0928, MNG1, RMSE2"	"Dicer, Drosophila, homolog of, 1"	DICER1	23405	ENSG00000100697		"Goiter, multinodular 1, with or without Sertoli-Leydig cell tumors, 138800 (3), Autosomal dominant; Pleuropulmonary blastoma, 601200 (3), Autosomal dominant; Rhabdomyosarcoma, embryonal, 2, 180295 (3)"	Dicer1 (MGI:2177178)			
chr14	95181938	95319907	14q32.13	14q32.13		611121	"CLMN, KIAA1188"	Calmin	CLMN	79789	ENSG00000165959			Clmn (MGI:2136957)			
chr14	95407265	95516692	14q32.13	14q32.13		610861	"SYNE3, C14orf49"	Spectrin repeat-containing nuclear envelope protein 3 (nesprin 3)	SYNE3	161176	ENSG00000176438			Syne3 (MGI:2442408)			
chr14	95534985	95544717	14q32	14q32.13		609588	"GLRX5, C14orf87, PRO1238, FLB4739, PRSA, SIDBA3, SPAHGC"	Glutaredoxin 5	GLRX5	51218	ENSG00000182512		"Anemia, sideroblastic, 3, pyridoxine-refractory, 616860 (3), Autosomal recessive; Spasticity, childhood-onset, with hyperglycinemia, 616859 (3), Autosomal recessive"	Glrx5 (MGI:1920296)			
chr14	95652096	95673451	14q32.1	14q32.13		604412	"TCL6, TNG1, TNG2"	T-cell leukemia/lymphoma 6	TCL6	27004							
chr14	95686416	95692642	14q32.1	14q32.13		603769	"TCL1B, TML1"	T-cell lymphoma/leukemia 1B	TCL1B	9623	ENSG00000213231		"Leukemia/lymphoma, T-cell, 603769 (2)"				
chr14	95694159	95714195	14q32.1	14q32.13		186960	"TCL1A, TCL1"	T-cell lymphoma/leukemia 1A	TCL1A	8115	ENSG00000100721		"Leukemia/lymphoma, T-cell, 186960 (2)"	Tcl1 (MGI:1097166)			
chr14	95876391	95925570	14q32	14q32.2		615719	"TUNAR, TUNA, LINC00617"	TCL1 upstream neural differentiation-associated RNA	TUNAR	100507043							
chr14	96204797	96244328	14q32.1-q32.2	14q32.2		113503	BDKRB2	Bradykinin receptor B2	BDKRB2	624	ENSG00000168398			Bdkrb2 (MGI:102845)			
chr14	96256209	96264762	14q32.1-q32.2	14q32.2		600337	BDKRB1	Bradykinin receptor B1	BDKRB1	623	ENSG00000100739			Bdkrb1 (MGI:88144)			
chr14	96279201	96363400	14q32.2	14q32.2		616226	ATG2B	"Autophagy 2, S. cerevisiae, homolog of, B"	ATG2B	55102	ENSG00000066739			Atg2b (MGI:1923809)			
chr14	96363451	96387289	14q32.2	14q32.2		616605	"GSKIP, C14orf129"	GSK3B-interacting protein	GSKIP	51527	ENSG00000100744			Gskip (MGI:1914037)			
chr14	96392087	96489426	14q32.2	14q32.2		615364	AK7	Adenylate kinase 7	AK7	122481	ENSG00000140057			Ak7 (MGI:1926051)			
chr14	96502375	96567115	14q32.1-q32.2	14q32.2		605553	"PAPOLA, PAP"	Poly(A) polymerase	PAPOLA	10914	ENSG00000090060			Papola (MGI:109301)			
chr14	96797346	96881613	14q32	14q32.2		602168	"VRK1, PCH1A"	Vaccinia-related kinase-1	VRK1	7443	ENSG00000100749		"Pontocerebellar hypoplasia type 1A, 607596 (3), Autosomal recessive"	Vrk1 (MGI:1261847)			
chr14	99169286	99271712	14q32.1	14q32.2		606558	"BCL11B, CTIP2, IMD49"	C-cell CLL/lymphoma 11B	BCL11B	64919	ENSG00000127152	mutation identified in 1 IMD49 patient	"?Immunodeficiency 49, 617237 (3), Autosomal dominant"	Bcl11b (MGI:1929913)			
chr14	99397745	99486457	14q32.2	14q32.2		615671	SETD3	SET domain-containing protein 3	SETD3	84193	ENSG00000183576			Setd3 (MGI:1289184)			
chr14	99481401	99511514	14q32	14q32.2		603544	CCNK	Cyclin K	CCNK	8812	ENSG00000090061			Ccnk (MGI:1276106)			
chr14	99684261	99727320	14q32.1	14q32.2		604087	"CYP46A1, CYP46"	"Cytochrome P450, family 46, subfamily A, polypeptide 1 (cholesterol 24-hydroxylase)"	CYP46A1	10858	ENSG00000036530			Cyp46a1 (MGI:1341877)			
chr14	99737698	99942059	14q32	14q32.2		602033	"EML1, EMAPL, EMAP, BH"	Echinoderm microtubule associated protein like 1	EML1	2009	ENSG00000066629		"Band heterotopia, 600348 (3), Autosomal recessive"	Eml1 (MGI:1915769)			
chr14	99971453	100144235	14q32.2	14q32.2		616912	EVL	ENAH/VASP-like protein	EVL	51466	ENSG00000196405			Evl (MGI:1194884)			
chr14	100146415	100166885	14q32.2	14q32.2		610862	"DEGS2, DES2"	"Delta(4)-desaturase, sphingolipid, 2"	DEGS2	123099	ENSG00000168350			Degs2 (MGI:1917309)			
chr14	100238764	100279033	14q	14q32.2		600013	"YY1, GADEVS"	YY1 transcription factor	YY1	7528	ENSG00000100811		"Gabriele-de Vries syndrome, 617557 (3), Autosomal dominant"	Yy1 (MGI:99150)			
chr14	100277985	100306546	14q32	14q32.2		615064	"SLC25A29, CACL, ORNT3"	"Solute carrier family 25 (carnitine/acylcarnitine translocase), member 29"	SLC25A29	123096	ENSG00000197119			Slc25a29 (MGI:2444911)			
chr14	100323336	100330420	14q32.31	14q32.2		609911	"HDMCP, C14orf68"	Hepatocellular carcinoma-downregulated mitochondrial carrier protein	SLC25A47	283600	ENSG00000140107			Slc25a47 (MGI:2144766)			
chr14	100333787	100376342	14q32.31	14q32.2		191050	"WARS, HMN9"	Tryptophanyl-tRNA synthetase	WARS	7453	ENSG00000140105		"Neuronopathy, distal hereditary motor, type IX, 617721 (3)"	Wars (MGI:104630)			
chr14	100726864	100738223	14q32	14q32.2		176290	"DLK1, PREF1, FA1"	"Delta, Drosophila, homolog-like 1"	DLK1	8788	ENSG00000185559			Dlk1 (MGI:94900)			
chr14	100826107	100861025	14q32.3	14q32.2		605636	"MEG3, GTL2"	Maternally expressed gene 3	MEG3	55384		100kb from DLK1					
chr14	100880654	100884846	14q32.2	14q32.2		611896	"RTL1, PEG11"	Retrotransposon-like gene 1	RTL1	388015	ENSG00000254656			Rtl1 (MGI:2656842)			
chr14	100881006	100881119	14q32.31	14q32.2		611708	"MIR431, MIRN431"	Micro RNA 431	MIR431	574038							
chr14	100881885	100881977	14q32.31	14q32.2		611711	"MIR433, MIRN433"	Micro RNA 433	MIR433	574034							
chr14	100882978	100883074	14q32.31	14q32.2		611709	"MIR127, MIRN127"	Micro RNA 127	MIR127	406914							
chr14	100884701	100884782	14q32.31	14q32.2		611710	"MIR136, MIRN136"	Micro RNA 136	MIR136	406927							
chr14	100889648	100999112	14q32	14q32.2-q32.3		613648	MEG8	Maternally expressed gene 8	MEG8	79104							
chr14	100897919	100897995	14q32	14q32.2		613649	SNORD112	"Small nucleolar, C/D box, 112"	SNORD112	692215		located in an intron of MEG8					
chr14	100911138	100911212	14q32.31	14q32.31		612553	"MIR370, MIRN370"	Micro RNA 370	MIR370	442915							
chr14	100924820	100924889	14q32	14q32.31		613650	SNORD113-1	"Small nucleolar RNA, C/D box, 113-1"	SNORD113-1	767561							
chr14	100949832	100949902	14q32	14q32.31		613651	SNORD114-1	"Small nucleolar RNA, C/D box, 114-1"	SNORD114-1	767577							
chr14	101022065	101022131	14q32.31	14q32.31		616358	MIR379	Micro RNA 379	MIR379	494328							
chr14	101025016	101025076	14q32	14q32.31		613654	"MIR380, MIRN380"	Micro RNA 380	MIR380	494329							
chr14	101029633	101029713	14q32.31	14q32.31		616036	MIR494	Micro RNA 494	MIR494	574452							
chr14	101033754	101033835	14q32.31	14q32.31		615149	MIR551A	Micro RNA 495	MIR495	574453							
chr14	101039689	101039754	14q32.31	14q32.31		610983	"MIR376C, MIR368"	Micro RNA 368C	MIR376C	442913							
chr14	101040068	101040147	14q32.31	14q32.31		610960	"MIR376A-2, MIRN376A-2"	Micro RNA 376A-2	MIR376A2	664615							
chr14	101040435	101040534	14q32.31	14q32.31		610961	"MIR376B, MIRN376B"	Micro RNA 376b	MIR376B	574435							
chr14	101040781	101040848	14q32.31	14q32.31		610959	"MIR376A-1, MIRN376A-1"	Micro RNA 376A-1	MIR376A1	494325							
chr14	101046454	101046537	14q32.31	14q32.31		615037	MIR487B	Micro RNA 487B	MIR487B	664616							
chr14	101054686	101054758	14q32.31	14q32.31		610164	MIR134	Micro RNA 134	MIR134	406924							
chr14	101055418	101055490	14q32.31	14q32.31		615385	MIR485	Micro RNA 485	MIR485	574436							
chr14	101065299	101065377	14q32.31	14q32.31		614057	"MIR409, MIRN409"	Micro RNA 409	MIR409	574413							
chr14	101065597	101065666	14q32.31	14q32.31		611794	"MIR369, MIR369-3, MIRN369-3"	Micro RNA 369	MIR369	442914							
chr14	101065911	101065990	14q32.31	14q32.31		615036	MIR410	Micro RNA 410	MIR410	574434							
chr14	101066723	101066800	14q32.31	14q32.31		616376	MIR656	Micro RNA 656	MIR656	724026							
chr14	101552220	101560421	14q32	14q32.31		608523	DIO3OS	"Deiodinase, iodothyronine, type 3, opposite strand"	DIO3OS	64150							
chr14	101561350	101563451	14q32	14q32.31		601038	"DIO3, TXDI3"	"Deiodinase, iodothyronine, type 3"	DIO3	1735	ENSG00000197406			Dio3 (MGI:1306782)			
chr14	101760572	101927991	14q32.31	14q32.31		601645	PPP2R5C	"Protein phosphatase-2, regulatory subunit B (B56), gamma isoform"	PPP2R5C	5527	ENSG00000078304	pseudogene on 3p21					
chr14	101964527	102050797	14q32	14q32.31		600112	"DYNC1H1, DNCL, DNECL, CMT20, MRD13, SMALED1"	"Dynein, cytoplasmic-1, heavy chain-1"	DYNC1H1	1778	ENSG00000197102		"Charcot-Marie-Tooth disease, axonal, type 20, 614228 (3), Autosomal dominant; Mental retardation, autosomal dominant 13, 614563 (3), Autosomal dominant; Spinal muscular atrophy, lower extremity-predominant 1, AD, 158600 (3), Autosomal dominant"	Dync1h1 (MGI:103147)			
chr14	102080737	102139748	14q32.2	14q32.31		140571	"HSP90AA1, HSPCA, HSPC1, HSP90A, HSP89A, HSPCAL4, LAP2"	"Heat-shock protein, 90kD, alpha, class A, member 1"	HSP90AA1	3320	ENSG00000080824			Hsp90aa1 (MGI:96250)			
chr14	102139365	102224685	14q32.31	14q32.31		617741	WDR20	WD repeat-containing protein 20	WDR20	91833	ENSG00000140153			Wdr20 (MGI:1916891)			
chr14	102224449	102305199	14q32	14q32.31		605762	"RAGE, MOK"	Renal tumor antigen	MOK	5891	ENSG00000080823			Mok (MGI:1336881)			
chr14	102348281	102362915	14q32.31	14q32.31		613362	CINP	CDK2-interacting protein	CINP	51550	ENSG00000100865			Cinp (MGI:1914486)			
chr14	102362911	102502480	14q32.31	14q32.31		615000	"TECPR2, KIAA0329, SPG49"	Tectonin beta-propeller repeat-containing protein 2	TECPR2	9895	ENSG00000196663		"Spastic paraplegia 49, autosomal recessive, 615031 (3), Autosomal recessive"	Tecpr2 (MGI:2144865)			
chr14	102592592	102730575	Chr.14	14q32.31-q32.32		607675	"RCOR, COREST, KIAA0071"	REST corepressor	RCOR1	23186	ENSG00000089902			Rcor1 (MGI:106340)			
chr14	102777478	102911499	14q32.32	14q32.32		601896	"TRAF3, CD40BP, LAP1, CAP1, CRAF1, IIAE5"	TNF receptor-associated factor 3	TRAF3	7187	ENSG00000131323	mutation identified in 1 IIAE5 patient	"{?Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 5}, 614849 (3)"	Traf3 (MGI:108041)			
chr14	102922429	102933596	14q32	14q32.32		605799	AMN	"Amnionless, mouse, homolog of"	AMN	81693	ENSG00000166126		"Megaloblastic anemia-1, Norwegian type, 261100 (3), Autosomal recessive"	Amn (MGI:1934943)			
chr14	102932378	103057404	14q32.3	14q32.32		614062	"CDC42BPB, MRCKB"	"CDC42-binding protein kinase, beta"	CDC42BPB	9578	ENSG00000198752			Cdc42bpb (MGI:2136459)			
chr14	103121174	103137438	14q32	14q32.32		603300	TNFAIP2	"Tumor necrosis factor, alpha-induced protein-2"	TNFAIP2	7127	ENSG00000185215			Tnfaip2 (MGI:104960)			
chr14	103334001	103345024	14q32.3	14q32.32		601710	EIF5	Eukaryotic translation initiation factor 5	EIF5	1983	ENSG00000100664			Eif5 (MGI:95309)			
chr14	103385363	103503830	14q32.3	14q32.32-q32.33		602678	MARK3	MAP/microtubule affinity-regulating kinase-3	MARK3	4140	ENSG00000075413			Mark3 (MGI:1341865)			
chr14	103500000	107043718	14q32.33			144120	IGHR	Immunoglobulin heavy chain regulator					"?Hyperimmunoglobulin G1 syndrome, 144120 (2), Autosomal dominant"				
chr14	103519657	103522858	14q32	14q32.33		123280	"CKB, CKBB, BCK"	"Creatine kinase, brain type"	CKB	1152	ENSG00000166165	distal to PI and AACT; closely linked to AKT1 and IGH; proximal to IGH		Ckb (MGI:88407)			
chr14	103562956	103592186	14q32.33	14q32.33		616003	"APOPT1, APOP"	"Apoptogenic protein 1, mitochondrial"	APOPT1	84334	ENSG00000256053		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Apopt1 (MGI:1915270)			
chr14	103629187	103701550	14q32.3	14q32.33		600025	"KLC1, KNS2, KNS2A"	"Kinesin, light chain 1"	KLC1	3831	ENSG00000126214			Klc1 (MGI:107978)			
chr14	103697610	103715485	14q32.3	14q32.33		600675	"XRCC3, CMM6"	"X-ray-repair, complementing defective, repair in Chinese hamster cells-3"	XRCC3	7517	ENSG00000126215		"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant; {Melanoma, cutaneous malignant, 6}, 613972 (3)"	Xrcc3 (MGI:1921585)			
chr14	103715743	103733667	14q32.33	14q32.33		613504	"ZFYVE21, ZF21"	Zinc finger FYVE domain-containing protein 21	ZFYVE21	79038	ENSG00000100711			Zfyve21 (MGI:1915770)			
chr14	103912287	103921565	14q32.33	14q32.33		604573	"C14orf2, MP68"	"MP68, rat, homolog of"	ATP5MPL	9556	ENSG00000156411			2010107E04Rik (MGI:1917507)			
chr14	104117404	104117513	14q32.33	14q32.33		611899	"MIR203, MIRN203"	Micro RNA 203	MIR203A	406986							
chr14	104138722	104180897	14q32.33	14q32.33		613231	"KIF26A, KIAA1236"	Kinesin family member 26A	KIF26A	26153	ENSG00000066735			Kif26a (MGI:2447072)			
chr14	104689605	104719609	14q32.33	14q32.33		610982	"INF2, FSGS5, C14orf173, CMTDIE"	Inverted formin 2	INF2	64423	ENSG00000203485		"Charcot-Marie-Tooth disease, dominant intermediate E, 614455 (3), Autosomal dominant; Glomerulosclerosis, focal segmental, 5, 613237 (3)"	Inf2 (MGI:1917685)			
chr14	104724196	104747324	14q32.33	14q32.33		612498	"ADSSL1, MPD5"	Adenylosuccinate synthase-like 1	ADSSL1	122622	ENSG00000185100		"Myopathy, distal, 5, 617030 (3), Autosomal recessive"	Adssl1 (MGI:87947)			
chr14	104769348	104795742	14q32.3	14q32.33		164730	"AKT1, CWS6"	Murine thymoma viral (v-akt) oncogene homolog-1	AKT1	207	ENSG00000142208	proximal to IGH	"Breast cancer, somatic, 114480 (3); Colorectal cancer, somatic, 114500 (3); Cowden syndrome 6, 615109 (3); Ovarian cancer, somatic, 167000 (3); Proteus syndrome, somatic, 176920 (3); {Schizophrenia, susceptibility to}, 181500 (2), Autosomal dominant"	Akt1 (MGI:87986)			
chr14	104800596	104804711	14q32.33	14q32.33		613915	"ZBTB42, ZNF925, LCCS6"	Zinc finger- and BTB domain-containing protein 42	ZBTB42	100128927	ENSG00000179627	mutation identified in 1 LCCS6 family	"?Lethal congenital contracture syndrome 6, 616248 (3), Autosomal recessive"	Zbtb42 (MGI:3644133)			
chr14	105009572	105021087	14q32.33	14q32.33		612270	"CDCA4, HEPP"	Cell division cycle-associated protein 4	CDCA4	55038	ENSG00000170779			Cdca4 (MGI:1919213)			
chr14	105049388	105065549	14q32.3	14q32.33		606167	"GPR132, G2A"	G protein-coupled receptor-132	GPR132	29933	ENSG00000183484			Gpr132 (MGI:1890220)			
chr14	105140980	105168823	14q32	14q32.33		602570	JAG2	Jagged 2	JAG2	3714	ENSG00000184916			Jag2 (MGI:1098270)			
chr14	105209285	105315576	14q32.33	14q32.33		604902	"BRF1, TAF3C, GTF3B, TF3B90, CFDS"	"BRF1, S. cerevisiae, homolog of (TATA box-binding protein-associated factor 3C)"	BRF1	2972	ENSG00000185024		"Cerebellofaciodental syndrome, 616202 (3), Autosomal recessive"	Brf1 (MGI:1919558)			
chr14	105300717	105398146	14q32.33	14q32.33		610423	"PACS2, KIAA0602"	Phosphofurin acidic cluster sorting protein 2	PACS2	23241	ENSG00000179364			Pacs2 (MGI:1924399)			
chr14	105419848	105470728	14q32.3	14q32.33		603526	MTA1	Metastasis-associated gene 1	MTA1	9112	ENSG00000182979			Mta1 (MGI:2150037)			
chr14	105472937	105480169	14q32.3	14q32.33		601183	"CRIP2, CRP2"	Cysteine-rich intestinal protein 2	CRIP2	1397	ENSG00000182809						
chr14	105486919	105488788	14q32.33	14q32.33		123875	"CRIP1, CRIP"	Cysteine-rich intestinal protein 1	CRIP1	1396	ENSG00000213145	previously assigned to 7q11.23		Crip1 (MGI:88501)			
chr14	105586436	106879843	14q32.33	14q32.33		146910	IGHD@	Immunoglobulin heavy chain diversity gene cluster	IGH	3492		many genes					
chr14	105586436	106879843	14q32.33	14q32.33		147010	IGHJ@	Immunoglobulin heavy chain joining gene cluster	IGH	3492		more than 4 genes					
chr14	105586436	106879843	14q32.33	14q32.33		147070	IGHV@	"Immunoglobin heavy polypeptide, variable gene cluster"	IGH	3492		"~250 genes; orientation: cen-PI-D14S1-IGH-IGHV--qter; 3' centromeric, 5' telomeric; IgM telomeric to IgG"					
chr14	105586936	105588393	14q32.33	14q32.33		147000	IGHA2	Constant region of heavy chain of IgA2	IGHA2	3494							
chr14	105600065	105601726	14q32.33	14q32.33		147180	IGHE	Constant region of heavy chain of IgE	IGHE	3497		pseudogene IGHEP1 nearby; IGHEP2 on chr.9					
chr14	105624475	105626064	14q32.33	14q32.33		147130	IGHG4	Constant region of heavy chain of IgG4	IGHG4	3503							
chr14	105643202	105644788	14q32.33	14q32.33		147110	IGHG2	Constant region of heavy chain of IgG2	IGHG2	3501		5'-G2-17kb-G4-3'; closeness of IGG3 and IGG1 known from Lepore-like myeloma protein	"IgG2 deficiency, selective (3)"				
chr14	105707167	105708663	14q32.33	14q32.33		146900	IGHA1	Constant region of heavy chain of IgA1	IGHA1	3493		Fused with IRTA1 in multiple myeloma					
chr14	105741472	105743069	14q32.33	14q32.33		147100	IGHG1	Constant region of heavy chain of IgG1	IGHG1	3500							
chr14	105765913	105771404	14q32.33	14q32.33		147120	IGHG3	Constant region of heavy chain of IgG3	IGHG3	3502							
chr14	105838400	105845676	14q32.33	14q32.33		147170	IGHD	Constant region of heavy chain of IgD	IGHD	3495							
chr14	105851965	105856216	14q32.33	14q32.33		147020	"IGHM, MU, AGM1"	Constant region of heavy chain of IgM	IGHM	3507			"Agammaglobulinemia 1, 601495 (3), Autosomal recessive"				
chr14	105914358	105914388	14q32.33	14q32.33		611937	"IGHD3-3, DXP4"	Immunoglobulin heavy chain diversity gene 3-3	IGHD3-3	28501							
chr14	105917978	105932641	14q32.33	14q32.33		616623	"KIAA0125, FAM30A, C14orf110"	"KIAA0125 gene, noncoding"	FAM30A	9834							
chr14	106268605	106269060	14q32.33	14q32.33		611939	"IGHV3-23, IGHV323, DP47, VH26"	Immunoglobulin heavy chain variable gene 3-23	IGHV3-23	28442							
chr14	0	107043718	Chr.14			151020	LCH	Lentil agglutinin-binding									
chr14	0	107043718	Chr.14			608251	PHOBS	"Phobia, specific"		404684			"Phobia, specific, 608251 (2)"				
chr14	0	107043718	Chr.14			616606	RC14S	Ring chromosome 14 syndrome					"Ring chromosome 14 syndrome, 616606 (4), Isolated cases"				
chr15	4200000	9700000	15p12			180452	RNR3	Ribosomal RNA-3	RNR3	6054							
chr15	19000000	25500000	15q11			608636	AUTS4	"Autism, susceptibility to, 4"					"{Autism susceptibility 4}, 608636 (2), Autosomal dominant"				
chr15	19000000	33400000	15q11-q13			607202	"CELIAC5, GSES"	"Celiac disease, susceptibility to, 5"		338332		in homogeneous Finnish population	"{Celiac disease, susceptibility to, 5}, 607202 (2)"				
chr15	19000000	33400000	15q11-q13			609745	GLC1I	"Glaucoma 1, open angle, I"	GLC1I	497188		max lod at GABRB3	"Glaucoma 1, open angle, I, 609745 (2)"				
chr15	19000000	101991189	15q11-qter			122460	HCVS	Human coronavirus sensitivity	HCVS	3063							
chr15	19000000	101991189	15q			604329	HYT2	"Hypertension, essential, susceptibility to, 2"		50986			"{Hypertension, essential, susceptibility to, 2}, 145500 (2), Multifactorial"				
chr15	19000000	27800000	15q11-q12			146990	IGHDY2	Immunoglobulin heavy chain diversity region-2		3496		?functional					
chr15	19000000	101991189	15q			214900	"LCS1, CHLS"	Cholestasis-lymphedema syndrome	LCS1	84565			"Cholestasis-lymphedema syndrome, 214900 (2), Autosomal recessive"				
chr15	19000000	67200000	15q11-q22			107254	MIC12	Antigen identified by monoclonal antibody 30.2A8	MIC12	4273		"in myoblasts, but not myotubes"					
chr15	19000000	27800000	15q11-q12			108990	MIC7	Attached cell antigen 28.3.7	MIC7	4270							
chr15	19000000	33400000	15q11-q13			603857	"MRKN3AS, ZNF127AS"	MKRN3 antisense RNA	MKRN3-AS1	10108							
chr15	19000000	49200000	15q11-q21.1			613328	RCHTS	Roifman-Chitayat syndrome		100462676		?1p36.23-p33	"?Roifman-Chitayat syndrome, 613328 (2), Autosomal recessive"				
chr15	20500000	25500000	15q11.2			615656	"DEL15q11.2, C15DELq11.2"	Chromosome 15q11.2 deletion syndrome				deleted region spans 300-500kb between BP1 and BP2	"Chromosome 15q11.2 deletion syndrome, 615656 (4), Autosomal dominant"				
chr15	20500000	27800000	15q11.2-q12			609179	MGR7	"Migraine with aura, susceptibility to, 7"		553992		between D15S113 and D15S1019	"{Migraine with aura, susceptibility to, 7}, 609179 (2)"				
chr15	20669467	20756150	15q11.2	15q11.2		601889	"NBEAP1, BCL8"	Neurobeachin pseudogene 1	NBEAP1	606							
chr15	22786224	22829788	15q11.1	15q11.2		608145	"NIPA1, SPG6"	Nonimprinted gene in Prader-Willi syndrome/Angelman syndrome chromosome region 1	NIPA1	123606	ENSG00000170113		"Spastic paraplegia 6, autosomal dominant, 600363 (3), Autosomal dominant"	Nipa1 (MGI:2442058)			
chr15	22838640	22868383	15q11.2	15q11.2		608146	NIPA2	Nonimprinted gene in Prader-Willi syndrome/Angelman syndrome chromosome region 2	NIPA2	81614	ENSG00000140157			Nipa2 (MGI:1913918)			
chr15	22867051	22980905	15q11	15q11.2		606322	"CYFIP1, KIAA0068"	Cytoplasmic FMRP interacting protein 1	CYFIP1	23191	ENSG00000273749			Cyfip1 (MGI:1338801)			
chr15	22983025	23039672	15q11.2	15q11.2		608147	"TUBGCP5, GCP5, KIAA1899"	Tubulin-gamma complex-associated protein 5	TUBGCP5	114791	ENSG00000275835			Tubgcp5 (MGI:2178836)			
chr15	23565306	23568019	15q11-q13	15q11.2		603856	"MKRN3, ZFP127, ZNF127, CPPB2"	Makorin 3	MKRN3	7681	ENSG00000179455	expressed only from paternal allele	"Precocious puberty, central, 2, 615346 (3), Autosomal dominant"	Mkrn3 (MGI:2181178)			
chr15	23643548	23647845	15q11.2	15q11.2		605283	"MAGEL2, NDNL1, SHFYNG"	MAGE-like 2	MAGEL2	54551	ENSG00000254585		"Schaaf-Yang syndrome, 615547 (3), Autosomal dominant"	Magel2 (MGI:1351648)			
chr15	23685406	23687302	15q11-q13	15q11.2		602117	NDN	Necdin	NDN	4692	ENSG00000182636		"Prader-Willi syndrome, 176270 (3), Isolated cases"	Ndn (MGI:97290)			
chr15	24164776	24169947	15q11.2	15q11.2		611217	PWRN2	Prader-Willi region noncoding RNA 2	PWRN2	791115							
chr15	24558156	24587779	15q11.2	15q11.2		611215	PWRN1	Prader-Willi region noncoding RNA 1	PWRN1	791114							
chr15	24675393	24683445	15q11.2	15q11.2		610922	"NPAP1, C15orf2"	Nuclear pore associated protein 1	NPAP1	23742	ENSG00000185823						
chr15	24823607	25419461	15q11.2	15q11.2		616259	"SNHG14, LNCAT, UBE3AATS"	Small nucleolar RNA host gene 14	SNHG14	104472715							
chr15	24823607	24978722	15q12	15q11.2		182279	SNRPN	Small nuclear ribonucleoprotein polypeptide N	SNRPN	6638	ENSG00000128739		"Prader-Willi syndrome, 176270 (3), Isolated cases"	Snrpn (MGI:98347)			
chr15	24984859	24988231	15q11-q13	15q11.2		600162	"D15S226E, PAR5"	Prader-Willi/Angelman syndrome-5	PWAR5	8123		paternally imprinted					
chr15	25051475	25051571	15q11.2	15q11.2		605436	"SNORD116-1, PWCR1"	"Small nucleolar RNA, C/D box, 116-1"	SNORD116-1	100033413							
chr15	25116544	25122475	15q11-q13	15q11.2		601491	IPW	Imprinted in Prader-Willi syndrome	IPW	3653							
chr15	25135641	25138052	15q11-q13	15q11.2		600161	"D15S227E, PAR1"	Prader-Willi/Angelman region-1	PWAR1	145624		paternally imprinted					
chr15	25170722	25170803	15q11.2	15q11.2		609837	"SNORD115-1, RNHBII52"	"Small nucleolar RNA, C/D box, 115-1"	SNORD115-1	338433							
chr15	25337233	25439380	15q11-q13	15q11.2		601623	"UBE3A, ANCR"	Ubiquitin protein ligase E3A	UBE3A	7337	ENSG00000114062	same location as PWS	"Angelman syndrome, 105830 (3), Isolated cases"	Ube3a (MGI:105098)			
chr15	25500000	27800000	15q12			610321	HPC7	"Prostate cancer, hereditary, 7"		100188809			"{Prostate cancer, hereditary, 7}, 610321 (2)"				
chr15	25500000	44500000	15q12-q15			605738	MCOPCB2	"Microphthalmia, isolated, with coloboma 2"		80771			"Microphthalmia with coloboma 2, 605738 (2)"				
chr15	25672240	25865143	15q11-q13	15q12		605855	"ATP10A, ATP10C, ATPVC"	"ATPase, class V, type 10A"	ATP10A	57194	ENSG00000206190			Atp10a (MGI:1330809)			
chr15	26543545	26773787	15q11.2-q12	15q12		137192	"GABRB3, ECA5, EIEE43"	"Gamma-aminobutyric acid (GABA) A receptor, beta-3"	GABRB3	2562	ENSG00000166206		"{Epilepsy, childhood absence, susceptibility to, 5}, 612269 (3); Epileptic encephalopathy, early infantile, 43, 617113 (3), Autosomal dominant"	Gabrb3 (MGI:95621)			
chr15	26866718	26949209	15q11.2-q12	15q12		137142	GABRA5	"Gamma-aminobutyric acid (GABA) A receptor, alpha-5"	GABRA5	2558	ENSG00000186297	100kb from GABRB3		Gabra5 (MGI:95617)			
chr15	26971281	27541118	15q11.2-q12	15q12		600233	GABRG3	"Gamma-aminobutyric acid (GABA) A receptor, gamma-3"	GABRG3	2567	ENSG00000182256	cen--G3--A5--B3		Gabrg3 (MGI:95624)			
chr15	27719007	28099341	15q11.2-q12	15q12-q13		611409	"OCA2, P, PED, D15S12, BOCA, EYCL3, HCL3, SHEP1"	"Pink-eye dilution, murine, homolog of (oculocutaneous albinism II)"	OCA2	4948	ENSG00000104044	?hypopigmentation in PWS and AS	"Albinism, brown oculocutaneous, 203200 (3), Autosomal recessive; Albinism, oculocutaneous, type II, 203200 (3), Autosomal recessive; [Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3), Autosomal recessive; [Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3), Autosomal recessive"	Oca2 (MGI:97454)			
chr15	27800000	44500000	15q13-q15			109710	B2MR	Beta-2-microglobulin regulator	B2MR	568							
chr15	27800000	42500000	15q13.1-q15.1			608646	CILD4	"Ciliary dyskinesia, primary, 4"		408257		between D15S1012 and D15S1048	"Ciliary dyskinesia, primary, 4, 608646 (2)"				
chr15	27800000	33400000	15q13			613025	SCZD13	Schizophrenia 13		100329170		associated with deletion at 15q13.3	"{Schizophrenia, susceptibility to, 13}, 613025 (2)"				
chr15	27800000	33400000	15q13			208500	"SRTD1, ATD1"	Short-rib thoracic dysplasia 1 with or without polydactyly	ATD	465			"Short-rib thoracic dysplasia 1 with or without polydactyly, 208500 (2), Autosomal recessive"				
chr15	28111036	28322172	15q13.1	15q13.1		605837	"HERC2, SHEP1, MRT38"	HECT domain and RCC1-like domain 2	HERC2	8924	ENSG00000128731	mutations in intron 4	"Mental retardation, autosomal recessive 38, 615516 (3), Autosomal recessive; [Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3), Autosomal recessive; [Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3), Autosomal recessive"	Herc2 (MGI:103234)			
chr15	28885478	29118314	15q	15q13.1		602712	APBA2	"Amyloid beta A4 precursor protein-binding, family A, member 2"	APBA2	321	ENSG00000034053			Apba2 (MGI:1261791)			
chr15	29268148	29269815	15q13.1	15q13.1		608243	"NSMCE3, NDNL2, MAGEG1, LICS"	"NSE3 homolog, SMC5-SMC6 complex component"	NSMCE3	56160	ENSG00000185115		"Lung disease, immunodeficiency, and chromosome breakage syndrome, 617241 (3), Autosomal recessive"	Nsmce3 (MGI:1913897)			
chr15	29699366	29968923	15q13	15q13.1		601009	TJP1	Tight junction protein 1 (zona occludens 1)	TJP1	7082	ENSG00000104067			Tjp1 (MGI:98759)			
chr15	30626147	30649181	15q13.2	15q13.2		616310	"ARHGAP11B, FAM7B1"	RHO GTPase-activating protein 11B	ARHGAP11B	89839	ENSG00000285077						
chr15	30900000	33400000	15q13.3			612001	"DEL15q13.3, MICRODEL15q13.3"	Chromosome 15q13.3 microdeletion syndrome					"Chromosome 15q13.3 microdeletion syndrome, 612001 (4)"				
chr15	30903851	30943107	15q13.2-q13.3	15q13.3		613534	"FAN1, MTMR15, KIAA1018, KMIN"	FANCD2/FANCI-associated nuclease 1	FAN1	22909	ENSG00000198690		"Interstitial nephritis, karyomegalic, 614817 (3), Autosomal recessive"	Fan1 (MGI:3045266)			
chr15	31001060	31161272	15q13-q14	15q13.3		603576	"TRPM1, MLSN1, CSNB1C"	"Transient receptor potential cation channel, subfamily M, member 1 (melastatin)"	TRPM1	4308	ENSG00000134160		"Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216 (3)"	Trpm1 (MGI:1330305)			
chr15	31065031	31065140	15q13.3	15q13.3		613753	"MIR211, MIRN211"	Micro RNA 211	MIR211	406993							
chr15	31326854	31435664	15q12	15q13.3		605328	"KLF13, RFLAT1, FKLF2"	Kruppel-like factor 13	KLF13	51621	ENSG00000169926			Klf13 (MGI:1354948)			
chr15	31475397	31870671	15q13.3	15q13.3		612024	"OTUD7A, OTUD7, C16orf15, CEZANNE2"	OTU domain-containing protein 7A	OTUD7A	161725	ENSG00000169918			Otud7a (MGI:2158505)			
chr15	32030461	32172520	15q14	15q13.3		118511	CHRNA7	"Cholinergic receptor, nicotinic, alpha polypeptide-7"	CHRNA7	1139	ENSG00000175344			Chrna7 (MGI:99779)			
chr15	32615143	32639936	15q13.2	15q13.3		610589	"ARHGAP11A, KIAA0013"	RHO GTPase-activating protein 11A	ARHGAP11A	9824	ENSG00000198826			Arhgap11a (MGI:2444300)			
chr15	32641612	32697097	15q11-q15	15q13.3		173120	"SCG5, SGNE1"	Secretogranin V (7B2 protein )	SCG5	6447	ENSG00000166922			Scg5 (MGI:98289)			
chr15	32718003	32734668	15q13-q15	15q13.3		603054	"GREM1, CKTSF1B1"	"Gremlin 1 homolog, cystine knot superfamily"	GREM1	26585	ENSG00000166923			Grem1 (MGI:1344337)			
chr15	32765543	33194764	15q13-q14	15q13.3		136535	"FMN, LD"	Formin (limb deformity)	FMN1	342184	ENSG00000248905			Fmn1 (MGI:101815)			
chr15	33310772	33866102	15q14-q15	15q13-q14		180903	RYR3	Ryanodine receptor-3	RYR3	6263	ENSG00000198838			Ryr3 (MGI:99684)			
chr15	33400000	39800000	15q14			616898	"DEL15q14, C15DELq14"	Chromosome 15q14 deletion syndrome					"Chromosome 15q14 deletion syndrome, 616898 (4), Autosomal dominant"				
chr15	33400000	39800000	15q14			604827	"EIG7, EJM2"	"Epilepsy, idiopathic generalized, susceptibility to, 7"	EJM2	50715		?role of CHRNA7	"{Epilepsy, idiopathic generalized, susceptibility to, 7}, 604827 (2), Autosomal recessive; Epilepsy, juvenile myoclonic, 604827 (2), Autosomal recessive"				
chr15	33968313	34065093	15q26	15q14		118496	CHRM5	"Cholinergic receptor, muscarinic, 5"	CHRM5	1133	ENSG00000184984			Chrm5 (MGI:109248)			
chr15	33851784	34074876	Chr.15	15q14		605265	AVEN	Cell death regulator AVEN	AVEN	57099	ENSG00000169857			Aven (MGI:1921518)			
chr15	34140673	34210095	15q14	15q14		616235	"KATNBL1, C15orf29"	"Katanin, p80 subunit, B-like 1"	KATNBL1	79768	ENSG00000134152			Katnbl1 (MGI:1919675)			
chr15	34224996	34230164	15q14	15q14		616245	"EMC4, TMEM85, PIG17"	ER membrane protein complex subunit 4	EMC4	51234	ENSG00000128463			Emc4 (MGI:1915282)			
chr15	34229995	34338063	15q13-q14	15q14		604878	"SLC12A6, KCC3A, KCC3B, KCC3, ACCPN"	"Solute carrier family 12 (potassium/chloride transporters), member 6"	SLC12A6	9990	ENSG00000140199		"Agenesis of the corpus callosum with peripheral neuropathy, 218000 (3), Autosomal recessive"	Slc12a6 (MGI:2135960)			
chr15	34341715	34343160	15q14-q15	15q14		606471	"NOLA3, NOP10, DKCB1"	"Nucleolar protein family A, member 3"	NOP10	55505	ENSG00000182117		"Dyskeratosis congenita, autosomal recessive 1, 224230 (3), Autosomal recessive"	Nop10 (MGI:1913431)			
chr15	34358887	34367195	15q14	15q14		612039	"AGPAT7, AYTL3"	1-acylglycerol-3-phosphate O-acyltransferase 7	LPCAT4	254531	ENSG00000176454			Lpcat4 (MGI:2138993)			
chr15	34379067	34437465	15q14	15q14		616180	"GOLGA8A, KIAA0855"	"Golgin A8 family, member A"	GOLGA8A	23015	ENSG00000175265						
chr15	34525275	34583650	15q14	15q14		609619	"GOLGA8B, KIAA0855"	"Golgi autoantigen, golgin subfamily A, 8B"	GOLGA8B	440270	ENSG00000215252						
chr15	34751745	34754954	15q14	15q14		607058	"GJD2, GJA9, CX36"	"Gap junction protein, delta-2 (connexin 36)"	GJD2	57369	ENSG00000159248			Gjd2 (MGI:1334209)			
chr15	34788095	34795725	15q14	15q14		102540	"ACTC1, CMD1R, CMH11, ASD5, LVNC4"	"Actin, alpha, cardiac muscle"	ACTC1	70	ENSG00000159251		"Atrial septal defect 5, 612794 (3), Autosomal dominant; Cardiomyopathy, dilated, 1R, 613424 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 11, 612098 (3), Autosomal dominant; Left ventricular noncompaction 4, 613424 (3), Autosomal dominant"	Actc1 (MGI:87905)			
chr15	34856350	34969793	15q14	15q14		610548	"AQR, IBP160, KIAA0560"	"Aquarius, mouse, homolog of"	AQR	9716	ENSG00000021776			Aqr (MGI:1276102)			
chr15	36579602	36810259	15q14	15q14		615626	C15orf41	Chromosome 15 open reading fram 41	C15orf41	84529	ENSG00000186073		"Dyserythropoietic anemia, congenital, type Ib, 615631 (3), Autosomal recessive"	BC052040 (MGI:3026886)			
chr15	36891020	37101298	15q14-q25	15q14		601740	"MEIS2, MRG1, CPCMR"	"Meis1, mouse, homolog of, 2"	MEIS2	4212	ENSG00000134138		"Cleft palate, cardiac defects, and mental retardation, 600987 (3), Autosomal dominant"	Meis2 (MGI:108564)			
chr15	38252086	38357248	15q13.2	15q14		609291	"SPRED1, NFLS"	Sprouty-related EVH1 domain-containing protein 1	SPRED1	161742	ENSG00000166068		"Legius syndrome, 611431 (3), Autosomal dominant"	Spred1 (MGI:2150016)			
chr15	38454126	38487709	15q14	15q14		616142	FAM98B	"Family with sequence similarity 98, member B"	FAM98B	283742	ENSG00000171262			Fam98b (MGI:1915465)			
chr15	38488096	38564805	15q15	15q14		603962	RASGRP1	Ras guanyl nucleotide releasing protein-1	RASGRP1	10125	ENSG00000172575			Rasgrp1 (MGI:1314635)			
chr15	39581078	39598917	15q15	15q14		188060	THBS1	Thrombospondin 1	THBS1	7057	ENSG00000137801			Thbs1 (MGI:98737)			
chr15	39597280	39782837	15q14	15q14		615795	"FSIP1, HSD10"	Fibrous sheath-interacting protein 1	FSIP1	161835	ENSG00000150667			Fsip1 (MGI:1918563)			
chr15	39795048	39920938	15q14-q15	15q14-q15		612183	GPR176	G protein-coupled receptor 176	GPR176	11245	ENSG00000166073			Gpr176 (MGI:2685858)			
chr15	39800000	44500000	15q15			605419	SCZD10	Schizophrenia 10	SCZD10	63944		between D15S1042 and D15S659	"{Schizophrenia 10}, 605419 (2), Autosomal dominant"				
chr15	39934100	40036152	15q15.1	15q15.1		609280	"EIF2AK4, GCN2, KIAA1338, PVOD2"	Eukaryotic translation initiation factor 2-alpha kinase 4	EIF2AK4	440275	ENSG00000128829		"Pulmonary venoocclusive disease 2, 234810 (3), Autosomal recessive"	Eif2ak4 (MGI:1353427)			
chr15	40035689	40039201	15q22	15q15.1		600708	SRP14	Signal recognition particle 14kD (homologous Alu RNA-binding protein)	SRP14	6727	ENSG00000140319			Srp14 (MGI:107169)			
chr15	40087889	40108883	15q14	15q15.1		606266	BMF	BCL2-modifying factor	BMF	90427	ENSG00000104081			Bmf (MGI:2176433)			
chr15	40161008	40221135	15q15	15q15.1		602860	"BUB1B, BUBR1, MVA1"	"Budding uninhibited by benzimidazoles 1, S. cerevisiae, homolog of, beta"	BUB1B	701	ENSG00000156970		"Colorectal cancer, somatic, 114500 (3); Mosaic variegated aneuploidy syndrome 1, 257300 (3), Autosomal recessive; [Premature chromatid separation trait], 176430 (3), Autosomal dominant"	Bub1b (MGI:1333889)			
chr15	40239090	40277486	15q15.1	15q15.1		608110	PAK6	p21-activated kinase 6	PAK6	56924	ENSG00000137843			Pak6 (MGI:2679420)			
chr15	40285495	40307972	15q15	15q15.1		604114	PLCB2	"Phospholipase C, beta-2"	PLCB2	5330	ENSG00000137841		Platelet PLC beta-2 deficiency (1)	Plcb2 (MGI:107465)			
chr15	40354358	40375988	Chr.15	15q15.1		607503	"DISPB, KIAA1742"	"Dispatched, Drosophila, homolog of, B"	DISP2	85455	ENSG00000140323			Disp2 (MGI:2388733)			
chr15	40382720	40394287	15q15.1	15q15.1		614718	"KNSTRN, C15orf23, SKAP"	Kinetochore-localized astrin/SPAG5 binding protein	KNSTRN	90417	ENSG00000128944			Knstrn (MGI:1289298)			
chr15	40405484	40435947	15q14-q15	15q15.1		607036	IVD	Isovaleryl Coenzyme A dehydrogenase	IVD	3712	ENSG00000128928		"Isovaleric acidemia, 243500 (3), Autosomal recessive"	Ivd (MGI:1929242)			
chr15	40439720	40468241	15q15.1	15q15.1		613880	"BAHD1, KIAA0945"	BROMO-adjacent homology domain-containing protein 1	BAHD1	22893	ENSG00000140320			Bahd1 (MGI:2139371)			
chr15	40470960	40473157	15q14	15q15.1		608429	"CHST14, D4ST1, ATCS, EDSMC1"	Carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14	CHST14	113189	ENSG00000169105		"Ehlers-Danlos syndrome, musculocontractural type 1, 601776 (3), Autosomal recessive"	Chst14 (MGI:1919386)			
chr15	40594011	40664341	15q15.1	15q15.1		609173	"KNL1, CASC5, AF15Q14, KIAA1570, D40, MCPH4"	Kinetochore scaffold 1	KNL1	57082	ENSG00000137812		"Microcephaly 4, primary, autosomal recessive, 604321 (3), Autosomal recessive"	Knl1 (MGI:1923714)			
chr15	40694773	40732339	15q15.1	15q15.1		179617	"RAD51A, RECA, MRMV2, FANCR"	"RAD51, S. cerevisiae, homolog of, A (E. coli RecA homolog)"	RAD51	5888	ENSG00000285396	mutation identified in 1 FANCR patient	"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant; ?Fanconi anemia, complementation group R, 617244 (3), Autosomal dominant; Mirror movements 2, 614508 (3), Autosomal dominant"	Rad51 (MGI:97890)			
chr15	40735883	40755335	15q15.1	15q15.1		611873	"FAM82A2, FAM82C, RMD3, PTPIP51"	"Family with sequence similarity 82, member A2"	RMDN3	55177	ENSG00000137824			Rmdn3 (MGI:1915059)			
chr15	40764086	40767712	15q15.1	15q15.1		602437	"GCHFR, GFRP"	GTP cyclohydrolase I feedback regulatory protein	GCHFR	2644	ENSG00000137880			Gchfr (MGI:2443977)			
chr15	40767447	40807477	15q15.1	15q15.1		616844	DNAJC17	"DNAJ/HSP40 homolog, subfamily C, member 17"	DNAJC17	55192	ENSG00000104129			Dnajc17 (MGI:1916658)			
chr15	40815444	40828792	15q15.1	15q15.1		613256	"PPP1R14D, GBPI1"	"Protein phosphatase 1, regulatory subunit 14D"	PPP1R14D	54866	ENSG00000166143			Ppp1r14d (MGI:1919362)			
chr15	40894409	40903974	15q15.1	15q15.1		608551	VPS18	"Vacuolar protein sorting 18, yeast, homolog of"	VPS18	57617	ENSG00000104142			Vps18 (MGI:2443626)			
chr15	40929332	40939059	15q21.1	15q15.1		605185	"DLL4, AOS6"	Delta-like 4	DLL4	54567	ENSG00000128917		"Adams-Oliver syndrome 6, 616589 (3), Autosomal dominant"	Dll4 (MGI:1859388)			
chr15	40942136	40956518	15q15.1	15q15.1		614587	CHAC1	"ChaC, E. coli, homolog of, 1"	CHAC1	79094	ENSG00000128965			Chac1 (MGI:1916315)			
chr15	40978879	41117777	15q15.1	15q15.1		610169	"INO80, INOC1"	INO80 complex subunit	INO80	54617	ENSG00000128908			Ino80 (MGI:1915392)			
chr15	41231155	41281886	15q13.3	15q15.1		606988	CHP	Calcineurin B homologous protein	CHP1	11261	ENSG00000187446			Chp1 (MGI:1927185)			
chr15	41332693	41381049	15q15.1	15q15.1		612818	"NUSAP1, ANKT, NUSAP"	Nucleolar and spindle-associated protein 1	NUSAP1	51203	ENSG00000137804			Nusap1 (MGI:2675669)			
chr15	41387348	41402500	15q13.3	15q15.1		606934	"NDUFAF1, CIA30, CGI65"	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, assembly factor 1"	NDUFAF1	51103	ENSG00000137806		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufaf1 (MGI:1916952)			
chr15	41417103	41483562	15q15.1	15q15.1		611633	"RTF1, KIAA0252"	"RTF1, S. cerevisiae, homolog of"	RTF1	23168	ENSG00000137815			Rtf1 (MGI:1309480)			
chr15	41493857	41503558	15q14-q21	15q15.1		147521	ITPKA	"Inositol 1,4,5-trisphosphate 3-kinase A"	ITPKA	3706	ENSG00000137825			Itpka (MGI:1333822)			
chr15	41503638	41513886	15q15.1-q21.1	15q15.1		151520	"LTK, TYK1"	Leukocyte tyrosine kinase	LTK	4058	ENSG00000062524			Ltk (MGI:96840)			
chr15	41517175	41544276	15q15.1	15q15.1		611475	"RPAP1, KIAA1403"	RNA polymerase II-associated protein 1	RPAP1	26015	ENSG00000103932			Rpap1 (MGI:1916175)			
chr15	41559021	41579337	15q15.1	15q15.1		600341	TYRO3	TYRO3 protein tyrosine kinase	TYRO3	7301	ENSG00000092445			Tyro3 (MGI:104294)			
chr15	41621224	41769942	15q15	15q15.1		616061	"MGA, KIAA0518"	MAX dimerization protein MGA	MGA	23269	ENSG00000174197			Mga (MGI:1352483)			
chr15	41774433	41827854	15q13	15q15.1		616786	"MAPKBP1, JNKBP1, NPHP20"	Mitogen-activated protein kinase-binding protein 1	MAPKBP1	23005	ENSG00000137802		"Nephronophthisis 20, 617271 (3), Autosomal recessive"	Mapkbp1 (MGI:1347004)			
chr15	41848145	41894076	15q21	15q15.1		605916	"SPTBN5, BSPECV"	"Spectrin, beta, non-erythrocytic 5"	SPTBN5	51332	ENSG00000137877			Sptbn5 (MGI:2685200)			
chr15	41838812	41848147	Chr.15	15q15.1		606088	PLA2G4B	"Phospholipase A2, group IVB"	PLA2G4B	100137049	ENSG00000243708			Pla2g4b (MGI:2384819)			
chr15	41899439	41972556	15q11.1	15q15.1		605892	EHD4	EH domain-containing 4	EHD4	30844	ENSG00000103966			Ehd4 (MGI:1919619)			
chr15	42067561	42094558	15q15	15q15.1		612864	PLA2G4D	"Phospholipase A2, Group IVD"	PLA2G4D	283748	ENSG00000159337			Pla2g4d (MGI:1925640)			
chr15	42158700	42208330	15q15.1	15q15.1		612188	"VPS39, VAM6, TLP, KIAA0770"	"Vacuolar protein sorting 39, yeast, homolog of"	VPS39	23339	ENSG00000166887			Vps39 (MGI:2443189)			
chr15	42273657	42353665	15q15.1-q15.2	15q15.1		104180	GANC	Neutral alpha-glucosidase C	GANC	2595	ENSG00000214013			Ganc (MGI:1923301)			
chr15	42359499	42412316	15q15.1-q21.1	15q15.1		114240	"CAPN3, CANP3"	"Calpain, large polypeptide L3"	CAPN3	825	ENSG00000092529		"Muscular dystrophy, limb-girdle, type 2A, 253600 (3), Autosomal recessive"	Capn3 (MGI:107437)			
chr15	42491243	42533060	15q21-q22	15q15.1-q15.2		602534	SNAP23	"Synaptosomal-associated protein, 23kD"	SNAP23	8773	ENSG00000092531			Snap23 (MGI:109356)			
chr15	42548812	42569993	15q15.2	15q15.2		613429	"HAUS2, CEP27"	"HAUS augmin-like complex, subunit 2"	HAUS2	55142	ENSG00000137814			Haus2 (MGI:1913546)			
chr15	42575609	42720997	15q15	15q15.2		614642	"STARD9, KIAA1300"	START domain-containing protein 9	STARD9	57519	ENSG00000159433			Stard9 (MGI:3045258)			
chr15	42723543	42737132	15q15	15q15.2		607465	"CDAN1, CDA1, CDAN1A"	Codanin 1	CDAN1	146059	ENSG00000140326		"Dyserythropoietic anemia, congenital, type Ia, 224120 (3), Autosomal recessive"	Cdan1 (MGI:1916218)			
chr15	42738973	42920994	15q15.2	15q15.2		611695	"TTBK2, SCA11"	Tau tubulin kinase 2	TTBK2	146057	ENSG00000128881		"Spinocerebellar ataxia 11, 604432 (3), Autosomal dominant"	Ttbk2 (MGI:2155779)			
chr15	42942896	43106087	15q15-q21.1	15q15.2		605981	"UBR1, JBS"	Ubiquitin-protein ligase E3-alpha	UBR1	197131	ENSG00000159459		"Johanson-Blizzard syndrome, 243800 (3), Autosomal recessive"	Ubr1 (MGI:1277977)			
chr15	43185117	43197176	Chr.15	15q15.2		607089	"CCNDBP1, GCIP"	Cyclin D-type-binding protein 1	CCNDBP1	23582	ENSG00000166946			Ccndbp1 (MGI:109595)			
chr15	43197226	43225855	15q15	15q15.2		177070	"EPB42, SPH5"	Erythrocyte surface protein band 4.2	EPB42	2038	ENSG00000166947		"Spherocytosis, type 5, 612690 (3)"	Epb42 (MGI:95402)			
chr15	43232594	43266856	15q15.2	15q15.2		603805	"TGM5, TGX, PSS2"	Transglutaminase 5	TGM5	9333	ENSG00000104055		"Peeling skin syndrome 2, 609796 (3), Autosomal recessive"	Tgm5 (MGI:1921426)			
chr15	43276276	43302254	15q15.2	15q15.2-q15.3		606776	"TGM7, TGMZ"	Transglutaminase 7	TGM7	116179	ENSG00000159495			Tgm7 (MGI:2151164)			
chr15	43300000	44500000	15q15.3			611102	"DEL15q15.3, C15DELq15.3"	Chromosome 15q15.3 deletion syndrome					"Deafness and male infertility, 611102 (4), Autosomal recessive"				
chr15	43300000	44500000	15q15.3			134600	"FRTS1, FRTS, RFS"	Fanconi renotubular syndrome		65211			"Fanconi renotubular syndrome 1, 134600 (2), Autosomal dominant"				
chr15	43300000	59000000	15q15.3-q22.1			601228	"HMPS1, CRAC1, CRCS4, DUP15q, C15DUPq"	"Polyposis syndrome, mixed, hereditary 1"				duplication of 40kb of 15q resulting in overexpression of GREM1	"{Colorectal cancer, susceptibility to, 4}, 601228 (4), Autosomal dominant; Polyposis syndrome, mixed hereditary 1, 601228 (4), Autosomal dominant"				
chr15	43327775	43330621	15q15.3	15q15.3		611246	"LCMT2, TYW4, KIAA0547"	Leucine carboxyl methyltransferase 2	LCMT2	9836	ENSG00000168806			Lcmt2 (MGI:1353659)			
chr15	43371058	43409770	15q15	15q15.3		609610	"TUBGCP4, GCP4, MCCRP3"	Tubulin-gamma complex-associated protein 4	TUBGCP4	27229	ENSG00000137822		"Microcephaly and chorioretinopathy, autosomal recessive, 3, 616335 (3), Autosomal recessive"	Tubgcp4 (MGI:1196293)			
chr15	43403063	43510727	15q15-q21	15q15.3		605230	"TP53BP1, 53BP1"	Tumor protein p53-binding protein-1	TP53BP1	7158	ENSG00000067369			Trp53bp1 (MGI:1351320)			
chr15	43517607	43531619	15q13-qter	15q15.3		600178	"MAP1A, MAP1L"	Microtubule-associated protein 1A	MAP1A	4130	ENSG00000166963			Map1a (MGI:1306776)			
chr15	43533461	43590271	15q15.3	15q15.3		610979	"PPIP5K1, HISPPD2A, IPS1, KIAA0377"	Diphosphoinositol pentakisphosphate kinase 1	PPIP5K1	9677	ENSG00000168781			Ppip5k1 (MGI:2443281)			
chr15	43592856	43599405	15q15	15q15.3		123290	"CKMT1B, CKMT1"	"Creatine kinase, mitochondrial 1B"	CKMT1B	1159	ENSG00000237289	centromeric to CKMT1A		Ckmt1 (MGI:99441)			
chr15	43599562	43618799	15q15	15q15.3		606440	"STRC, DFNB16"	Stereocilin	STRC	161497	ENSG00000242866		"Deafness, autosomal recessive 16, 603720 (3), Autosomal recessive"	Strc (MGI:2153816)			
chr15	43630561	43648883	15q15.1-q15.3	15q15.3		607249	CATSPER2	"Cation channel, sperm-associated, 2"	CATSPER2	117155	ENSG00000166762	in region with tandem duplication containing a CATSPER2 pseudogene		Catsper2 (MGI:2387404)			
chr15	43692643	43699221	15q15	15q15.3		613415	CKMT1A	"Creatine kinase, mitochondrial 1A"	CKMT1A	548596	ENSG00000223572	telomeric to CKMT1B		Ckmt1 (MGI:99441)			
chr15	43746391	43772605	15q15	15q15.3		602046	GRP58	"Glucose regulated protein, 58kD"	PDIA3	2923	ENSG00000167004			Pdia3 (MGI:95834)			
chr15	43772599	43777303	15q15.3	15q15.3		609885	ELL3	"Elongation factor, RNA polymerase II, 3"	ELL3	80237	ENSG00000128886			Ell3 (MGI:2673679)			
chr15	43777095	43796088	15q14.3	15q15.3		605054	"SERF2, H4F5REL"	Small EDRK-rich factor 2	SERF2	10169	ENSG00000140264			Serf2 (MGI:1337041)			
chr15	43794173	43800096	15q15.3	15q15.3		614550	SERINC4	Serine incorporator 4	SERINC4	619189	ENSG00000184716			Serinc4 (MGI:2441842)			
chr15	43800420	43802588	15q15.3	15q15.3		612784	HYPK	Huntingtin-interacting protein K	HYPK	25764	ENSG00000242028			Hypk (MGI:1914943)			
chr15	43804534	43824752	15q15-q12	15q15.3		600215	MFAP1	Microfibrillar-associated protein-1	MFAP1	4236	ENSG00000140259			"Mfap1a,Mfap1b (MGI:3694697,MGI:1914782)"			
chr15	43870760	44195293	15q15.3	15q15.3		616309	FRMD5	FERM domain-containing protein 5	FRMD5	84978	ENSG00000171877			Frmd5 (MGI:2442557)			
chr15	44500000	58800000	15q21			105600	"CDAN3, CDA3"	"Congenital dyserythropoietic anemia, type III"	CDAN3	981			"Dyserythropoietic anemia, congenital, type III, 105600 (2), Autosomal dominant"				
chr15	44500000	67200000	15q21-q22			605728	"CTRCT25, CCSSO"	Cataract 25		80770			"Cataract 25, 605728 (2)"				
chr15	44537067	44562802	15q15.3	15q21.1		603910	"EIF3J, EIF3S1"	"Eukaryotic translation initiation factor 3, subunit J"	EIF3J	8669	ENSG00000104131			"Eif3j2,Eif3j1 (MGI:1925905,MGI:3704486)"			
chr15	44562695	44663677	15q21.1	15q21.1		610844	"SPG11, KIAA1840, FLJ21439, ALS5, CMT2X"	Spastascin	SPG11	80208	ENSG00000104133		"Amyotrophic lateral sclerosis 5, juvenile, 602099 (3), Autosomal recessive; Charcot-Marie-Tooth disease, axonal, type 2X, 616668 (3), Autosomal recessive; Spastic paraplegia 11, autosomal recessive, 604360 (3), Autosomal recessive"	Spg11 (MGI:2444989)			
chr15	44665731	44711405	15q21.1	15q21.1		614661	"PATL2, PAT1A, OOMD4"	"Protein associated with topoisomerase II, S. Cerevisiae, homolog of"	PATL2	197135	ENSG00000229474		"Oocyte maturation defect 4, 617743 (3), Autosomal recessive"	Patl2 (MGI:1914828)			
chr15	44711486	44718158	15q21-q22	15q21.1		109700	"B2M, IMD43"	Beta-2-microglobulin	B2M	567	ENSG00000166710	mutation identified in 1 FVA family	"?Amyloidosis, familial visceral, 105200 (3), Autosomal dominant; Immunodeficiency 43, 241600 (3), Autosomal recessive"	B2m (MGI:88127)			
chr15	44736361	44767828	15q21.1	15q21.1		616017	"TRIM69, TRIF, RNF36"	Tripartite motif-containing protein 69	TRIM69	140691	ENSG00000185880			Trim69 (MGI:1918178)			
chr15	44956673	44979222	15q21.1	15q21.1		617131	"TERB2, C15orf43"	Telomere repeat-binding bouquet formation protein 2	TERB2	145645	ENSG00000167014			Terb2 (MGI:1921651)			
chr15	45023103	45075088	15q15.3	15q21.1		182500	"SORD, SORD1"	Sorbitol dehydrogenase	SORD	6652	ENSG00000140263		"?Cataract, congenital, 182500 (2)"	Sord (MGI:98266)			
chr15	45092647	45114160	15q15.3	15q21.1		606759	"DUOX2, THOX2, TDH6"	Dual oxidase 2 (thyroid oxidase 2)	DUOX2	50506	ENSG00000140279		"Thyroid dyshormonogenesis 6, 607200 (3), Autosomal recessive"	Duox2 (MGI:3036280)			
chr15	45114320	45118105	15q15	15q21.1		612772	"DUOXA2, TDH5"	Dual oxidase maturation factor 2	DUOXA2	405753	ENSG00000140274	head-to-head with DUOX2	"Thyroid dyshormonogenesis 5, 274900 (3), Autosomal recessive"	Duoxa2 (MGI:1914061)			
chr15	45117365	45129937	15q15	15q21.1		612771	DUOXA1	Dual oxidase maturation factor 1	DUOXA1	90527	ENSG00000140254	tail-to-tail with DUOXA2		Duoxa1 (MGI:2384861)			
chr15	45129993	45165577	15q15.3	15q21.1		606758	"DUOX1, THOX1"	Dual oxidase 1 (thyroid oxidase 1)	DUOX1	53905	ENSG00000137857			Duox1 (MGI:2139422)			
chr15	45167213	45201174	15q21.1	15q21.1		617313	SHF	SH2 domain-containing adaptor protein F	SHF	90525	ENSG00000138606			Shf (MGI:3613669)			
chr15	45252229	45275933	15q15	15q21.1		606208	"SLC28A2, CNT2, SPNT1"	"Solute carrier family 28 (sodium-coupled nucleoside transporter), member 2"	SLC28A2	9153	ENSG00000137860			Slc28a2 (MGI:1913105)			
chr15	45361123	45402316	15q21.1	15q21.1		602360	"GATM, AGAT, CCDS3"	L-arginine:glycine amidinotransferase	GATM	2628	ENSG00000171766		"Cerebral creatine deficiency syndrome 3, 612718 (3), Autosomal recessive"	Gatm (MGI:1914342)			
chr15	45430528	45433448	15q21.1	15q21.1		608409	NMES1	Normal mucosa of esophagus-specific gene 1	C15orf48	84419	ENSG00000166920			AA467197 (MGI:3034182)			
chr15	45479612	45523754	15q21.1	15q21.1		602095	"SLC30A4, ZNT4"	"Solute carrier family 30 (zinc transporter), member 4"	SLC30A4	7782	ENSG00000104154			Slc30a4 (MGI:1345282)			
chr15	45511135	45556729	15q21.1	15q21.1		611314	"HMGN2P46, C15orf21"	High mobility group nucleosomal binding domain 2 pseudogene 46	HMGN2P46	283651							
chr15	45587122	45609715	15q15	15q21.1		604310	"BLOC1S6, BLOS6, PLDN, PA, HPS9"	"Biogenesis of lysosome-related organelles complex 1, subunit 6"	BLOC1S6	26258	ENSG00000104164	mutation identified in 1 HPS9 patient	"?Hermansky-pudlak syndrome 9, 614171 (3), Autosomal recessive"	Bloc1s6 (MGI:1927580)			
chr15	45631147	45691293	15q21.1	15q21.1		617658	"SQOR, SQRDL"	Sulfide quinone oxidoreductase	SQOR	58472	ENSG00000137767			Sqor (MGI:1929899)			
chr15	47184097	47774222	15q21.1	15q21.1		609295	"SEMA6D, KIAA1479"	Semaphorin 6D	SEMA6D	80031	ENSG00000137872			Sema6d (MGI:2387661)			
chr15	48120971	48142391	15q21.1	15q21.1		609802	"SLC24A5, NCKX5, SHEP4, OCA6"	"Solute carrier family 24 (sodium/potassium/calcium exchanger), member 5"	SLC24A5	283652	ENSG00000188467		"Albinism, oculocutaneous, type VI, 113750 (3), Autosomal recessive; [Skin/hair/eye pigmentation 4, fair/dark skin], 113750 (3), Autosomal recessive"	Slc24a5 (MGI:2677271)			
chr15	48206300	48304077	15q15-q21.1	15q21.1		600839	"SLC12A1, NKCC2"	"Solute carrier family 12 (sodium/potassium/chloride transporters), member 1"	SLC12A1	6557	ENSG00000074803		"Bartter syndrome, type 1, 601678 (3), Autosomal recessive"	Slc12a1 (MGI:103150)			
chr15	48329990	48343372	15q15-q21.1	15q21.1		601266	DUT	dUTP pyrophosphatase	DUT	1854	ENSG00000128951			Dut (MGI:1346051)			
chr15	48408305	48645787	15q21.1	15q21.1		134797	"FBN1, MFS1, WMS2, SSKS, GPHYSD2, ACMICD, ECTOL1, MFLS"	Fibrillin-1	FBN1	2200	ENSG00000166147		"Acromicric dysplasia, 102370 (3), Autosomal dominant; Ectopia lentis, familial, 129600 (3), Autosomal dominant; Geleophysic dysplasia 2, 614185 (3), Autosomal dominant; MASS syndrome, 604308 (3); Marfan lipodystrophy syndrome, 616914 (3), Autosomal dominant; Marfan syndrome, 154700 (3), Autosomal dominant; Stiff skin syndrome, 184900 (3), Autosomal dominant; Weill-Marchesani syndrome 2, dominant, 608328 (3), Autosomal dominant"	Fbn1 (MGI:95489)			
chr15	48662533	48811903	15q21.1	15q21.1		613529	"CEP152, KIAA0912, MCPH9, SCKL5"	"Centrosomal protein, 152kD"	CEP152	22995	ENSG00000103995		"Microcephaly 9, primary, autosomal recessive, 614852 (3), Autosomal recessive; Seckel syndrome 5, 613823 (3), Autosomal recessive"	Cep152 (MGI:2139083)			
chr15	48823736	48963443	15q21.1	15q21.1		617372	"SHC4, RALP, SHCD"	SHC transforming protein 4	SHC4	399694	ENSG00000185634			Shc4 (MGI:2655364)			
chr15	48878092	48880182	15q21.1-q21.2	15q21.1		605894	"EID1, CRI1, C15orf3"	EP300-interacting inhibitor of differentiation 1	EID1	23741	ENSG00000255302			Eid1 (MGI:1889651)			
chr15	48988637	49046562	15q21.1	15q21.1		615756	"SECISBP2L, SBP2L, KIAA0256"	Selenocysteine insertion sequence-binding protein 2-like	SECISBP2L	9728	ENSG00000138593			Secisbp2l (MGI:1917604)			
chr15	49125273	49155656	15q21.2	15q21.1		604508	"TRIP15, SGN2, COPS2"	Thyroid hormone receptor interactor-15	COPS2	9318	ENSG00000166200						
chr15	49155758	49367882	Chr.15	15q21.1-q21.2		137028	"GALK2, GK2"	Galactokinase-2	GALK2	2585	ENSG00000156958			Galk2 (MGI:1917226)			
chr15	49423177	49487325	15q15-q21.1	15q21.2		148180	FGF7	Fibroblast growth factor-7 (keratinocyte growth factor)	FGF7	2252	ENSG00000140285			Fgf7 (MGI:95521)			
chr15	50182195	50236391	15q21.2	15q21.2		603247	"SLC27A2, FACVL1, VLACS"	"Solute carrier family 27 (fatty acid transporter), member 2 (fatty acid CoA ligase, very long-chain 1)"	SLC27A2	11001	ENSG00000140284			Slc27a2 (MGI:1347099)			
chr15	50241944	50266048	15q21-q22	15q21.2		142704	HDC	Histidine decarboxylase	HDC	3067	ENSG00000140287		"{Gilles de la Tourette syndrome, susceptibility to}, 137580 (3), Autosomal dominant"	Hdc (MGI:96062)			
chr15	50277191	50359305	15q21.2	15q21.2		600610	"GABPB, BABPB2, GABPB1, E4TF1B, NRF2B1"	"GA-binding protein transcription factor, beta subunit"	GABPB1	2553	ENSG00000104064			Gabpb1 (MGI:95611)			
chr15	50424358	50501082	15q21.2	15q21.2		603158	"USP8, HUMORF8, PITA4"	Ubiquitin-specific protease 8	USP8	9101	ENSG00000138592		"Pituitary adenoma 4, ACTH-secreting, somatic, 219090 (3)"	Usp8 (MGI:1934029)			
chr15	50557157	50686814	15q21	15q21.2		605692	"TRPM7, LTRPC7, CHAK, ALSPDC"	"Transient receptor potential cation channel, subfamily M, member 7"	TRPM7	54822	ENSG00000092439		"{Amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to}, 105500 (3), Autosomal dominant"	Trpm7 (MGI:1929996)			
chr15	50702265	50765712	15q15.3	15q21.2		608238	"SPPL2A, IMP3"	Signal peptide peptidase-like 2A	SPPL2A	84888	ENSG00000138600			Sppl2a (MGI:1913802)			
chr15	50908568	51005899	15q21.2	15q21.2		607244	"AP4E1, SPG51, CPSQ4, STUT1"	"Adaptor-related protein complex 4, epsilon-1 subunit"	AP4E1	23431	ENSG00000081014		"Spastic paraplegia 51, autosomal recessive, 613744 (3), Autosomal recessive; Stuttering, familial persistent, 1, 184450 (3), Autosomal dominant"	Ap4e1 (MGI:1336993)			
chr15	51056595	51105275	15q21.2	15q21.2		616438	"TNFAIP8L3, TIPE3"	Tumor necrosis factor-alpha-induced protein 8-like 3	TNFAIP8L3	388121	ENSG00000183578			Tnfaip8l3 (MGI:2685363)			
chr15	51208056	51338597	15q21.1	15q21.2		107910	"CYP19A1, CYP19, ARO"	"Cytochrome P450, family 19, subfamily A, polypeptide 1 (aromatization of androgens)"	CYP19A1	1588	ENSG00000137869	close to CYP11 in mouse	"Aromatase deficiency, 613546 (3); Aromatase excess syndrome, 139300 (3), Autosomal dominant"	Cyp19a1 (MGI:88587)			
chr15	51341503	51413364	15q21.2	15q21.2		608603	"GLDN, CRGL2, LCCS11"	Gliomedin	GLDN	342035	ENSG00000186417		"Lethal congenital contracture syndrome 11, 617194 (3), Autosomal recessive"	Gldn (MGI:2388361)			
chr15	51447723	51622832	15q21.2	15q21.2		612186	"DMXL2, RC3, KIAA0856, PEPNS, DFNA71"	DMX-like 2	DMXL2	23312	ENSG00000104093	mutation identified in 1 PEPNS family and 1 DFNA71 family	"?Deafness, autosomal dominant 71, 617605 (3), Autosomal dominant; ?Polyendocrine-polyneuropathy syndrome, 616113 (3), Autosomal recessive"	Dmxl2 (MGI:2444630)			
chr15	51681352	51721025	15q21.3	15q21.2		611796	SCG3	Secretogranin III	SCG3	29106	ENSG00000104112			Scg3 (MGI:103032)			
chr15	51751560	51816362	15q21.1-q21.2	15q21.2		602928	TMOD2	"Tropomodulin 2, neuronal"	TMOD2	29767	ENSG00000128872			Tmod2 (MGI:1355335)			
chr15	51829627	51912137	15q21.1-q21.2	15q21.2		605112	TMOD3	Tropomodulin 3	TMOD3	29766	ENSG00000138594			Tmod3 (MGI:1355315)			
chr15	51938023	51971800	15q15.3	15q21.2		610507	"LEO1, RDL"	"LEO1 RNA polymerase II associated factor, S. cerevisiae, homolog of"	LEO1	123169	ENSG00000166477			Leo1 (MGI:2685031)			
chr15	52109262	52112774	15q21	15q21.2		606910	BCL2L10	BCL2-like 10	BCL2L10	10017	ENSG00000137875			Bcl2l10 (MGI:1330841)			
chr15	52120925	52191367	15q21.2	15q21.2		604447	"GNB5, GB5, IDDCA, LADCI"	"Guanine nucleotide-binding protein, beta-5"	GNB5	10681	ENSG00000069966		"Intellectual developmental disorder with cardiac arrhythmia, 617173 (3), Autosomal recessive; Language delay and ADHD/cognitive impairment with or without cardiac arrhythmia, 617182 (3), Autosomal recessive"	Gnb5 (MGI:101848)			
chr15	52192317	52295797	15q21	15q21.2		610022	MYO5C	Myosin Vc	MYO5C	55930	ENSG00000128833			Myo5c (MGI:2442485)			
chr15	52307282	52529049	15q21	15q21.2		160777	"MYO5A, MYH12, GS1"	Myosin Va	MYO5A	4644	ENSG00000197535		"Griscelli syndrome, type 1, 214450 (3), Autosomal recessive"	Myo5a (MGI:105976)			
chr15	52547044	52569445	Chr.15	15q21.2		605487	"ARPP19, ARPP16"	"cAMP-regulated phosphoprotein, 19kD"	ARPP19	10776	ENSG00000128989			Arpp19 (MGI:1891691)			
chr15	52755052	52790263	15q21.1-q21.2	15q21.3		604164	"ONECUT1, HNF6A, HNF6"	"One cut domain, family member 1 (hepatocyte nuclear factor 6-alpha)"	ONECUT1	3175	ENSG00000169856			Onecut1 (MGI:1196423)			
chr15	53513740	53762877	15q21.3	15q21.3		613214	"WDR72, AI2A3"	WD repeat-containing protein 72	WDR72	256764	ENSG00000166415		"Amelogenesis imperfecta, type IIA3, 613211 (3), Autosomal recessive"	Wdr72 (MGI:3583957)			
chr15	53837572	54628607	15q21.3	15q21.3		614568	UNC13C	"Unc13, C. elegans, homolog of, C"	UNC13C	440279	ENSG00000137766			Unc13c (MGI:2149021)			
chr15	55181313	55197032	15q21.3	15q21.3		613262	"RSL24D1, RLP24"	Ribosomal protein L24 domain-containing protein 1	RSL24D1	51187	ENSG00000137876			Rsl24d1 (MGI:2681840)			
chr15	55202965	55291337	15q21	15q21.3		603868	"RAB27A, RAM, GS2"	Ras-associated protein RAB27A	RAB27A	5873	ENSG00000069974		"Griscelli syndrome, type 2, 607624 (3), Autosomal recessive"	Rab27a (MGI:1861441)			
chr15	55318934	55355647	15q21-q22	15q21.3		604122	PIGB	"Phosphatidylinositol glycan, class B"	PIGB	9488	ENSG00000069943			Pigb (MGI:1891825)			
chr15	55355222	55408509	15q21.3	15q21.3		611326	"CCPG1, KIAA1254, CPR8"	Cell cycle progression 1	CCPG1	9236	ENSG00000260916			Ccpg1 (MGI:1196419)			
chr15	55417754	55508233	15q21	15q21.3		608706	"DNAAF4, DYX1C1, DYXC1, DYX1, CILD25"	"Dynein, axonemal, assembly factor 4"	DNAAF4	161582	ENSG00000256061	not confirmed by some studies	"Ciliary dyskinesia, primary, 25, 615482 (3), Autosomal recessive; {Dyslexia, susceptibility to, 1}, 127700 (3), Autosomal dominant"	Dyx1c1 (MGI:1914935)			
chr15	55611539	55743123	15q21.3	15q21.3		613261	PRTG	"Protogenin, chicken, homolog of"	PRTG	283659	ENSG00000166450			Prtg (MGI:2444710)			
chr15	55826916	55993745	15q	15q21.3		602278	NEDD4	"Neural precursor cell expressed, developmentally downregulated-4"	NEDD4	4734	ENSG00000069869						
chr15	56090532	56247653	15q21.3	15q21.3		612660	"RFX7, RFXDC2"	"Regulatory factor X, 7"	RFX7	64864	ENSG00000181827			Rfx7 (MGI:2442675)			
chr15	56428730	56465136	15q21.3	15q21.3		610766	"MNS1, FLJ11222"	Meiosis-specific nuclear structural protein 1	MNS1	55329	ENSG00000138587			Mns1 (MGI:107933)			
chr15	56918089	57292594	15q21	15q21.3		600480	"TCF12, HTF4, CRS3"	"Transcription factor-12 (HTF4, helix-loop-helix transcription factors-4)"	TCF12	6938	ENSG00000140262		"Craniosynostosis 3, 615314 (3), Autosomal dominant"	Tcf12 (MGI:101877)			
chr15	57376457	57550726	15q21.2-q21.3	15q21.3		607856	"CGNL1, FLJ14957, KIAA1749"	Cingulin-like 1	CGNL1	84952	ENSG00000128849			Cgnl1 (MGI:1915428)			
chr15	57591903	57685363	15q21.3-q22.1	15q21.3		614071	"GUP, GCOM1, MYOZAP"	GRINL1A complex locus upstream gene	MYZAP	100820829	ENSG00000263155			Myzap (MGI:2142908)			
chr15	57706520	57717556	15q22.1	15q21.3		606485	"POLR2M, GDOWN, GRINL1A"	"Polymerase II, RNA, subunit M"	POLR2M	81488	ENSG00000255529			Polr2m (MGI:107282)			
chr15	57953423	58065922	15q21.3	15q21.3		603687	"ALDH1A2, RALDH2"	"Aldehyde dehydrogenase 1 family, member A2 (retinaldehyde dehydrogenase 2)"	ALDH1A2	8854	ENSG00000128918			Aldh1a2 (MGI:107928)			
chr15	58138168	58185910	15q22	15q21.3		602914	AQP9	Aquaporin 9	AQP9	366	ENSG00000103569			Aqp9 (MGI:1891066)			
chr15	58410456	58568951	15q21.3	15q21.3		151670	"LIPC, HL, LIPH, HDLCQ12"	"Lipase C, hepatic"	LIPC	3990	ENSG00000166035		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant; Hepatic lipase deficiency, 614025 (3), Autosomal recessive; [High density lipoprotein cholesterol level QTL 12], 612797 (3)"	Lipc (MGI:96216)			
chr15	58595203	58749977	15q21.3	15q21.3		602192	"ADAM10, MADM, RAK, AD18"	A disintegrin and metalloprotease domain 10	ADAM10	102	ENSG00000137845		"{Alzheimer disease 18, susceptibility to}, 615590 (3); Reticulate acropigmentation of Kitamura, 615537 (3), Autosomal dominant"	Adam10 (MGI:109548)			
chr15	58800000	78000000	15q22-q24			611274	GLC1N	"Glaucoma 1, open angle, N"	GLC1N	777645		max lod at D15S125	"Glaucoma 1, open angle, N, 611274 (2)"				
chr15	58800000	72400000	15q22-q23			612632	USH1H	"Usher syndrome, type 1H"	USH1H	100271837		max lod at D15S980	"Usher syndrome, type 1H, 612632 (2)"				
chr15	58987587	59097418	15q22.1-q22.2	15q22.1-q22.2		605840	RNF111	Ring finger protein 111	RNF111	54778	ENSG00000157450			Rnf111 (MGI:1934919)			
chr15	59105084	59125044	15q22.2	15q22.2		602755	CCNB2	Cyclin B2	CCNB2	9133	ENSG00000157456			Ccnb2 (MGI:88311)			
chr15	59135968	59372871	15q21-q22	15q22.2		601479	"MYO1E, MYO1C, FSGS6"	Myosin IE	MYO1E	4643	ENSG00000157483		"Glomerulosclerosis, focal segmental, 6, 614131 (3), Autosomal recessive"	Myo1e (MGI:106621)			
chr15	59611782	59620010	15q21.3	15q22.2		606836	GCNT3	"Glucosaminyl (N-acetyl) transferase 3, mucin-type"	GCNT3	9245	ENSG00000140297			Gcnt3 (MGI:1919327)			
chr15	59638061	59657540	15q22.2	15q22.2		600519	"GTF2A2, TF2A2"	"General transcription factor IIA, gamma subunit"	GTF2A2	2958	ENSG00000140307	"pseudogenes on chr. 1, 8, 9"		Gtf2a2 (MGI:1933289)			
chr15	59659145	59689533	15q22.2	15q22.2		603292	"BNIP2, NIP2"	BCL2/adenovirus E1B 19kD protein-interacting protein 2	BNIP2	663	ENSG00000140299			Bnip2 (MGI:109327)			
chr15	60347150	60398024	15q21-q22	15q22.2		151740	"ANXA2, ANX2L4, LPC2D, LIP2"	Annexin A2 (lipocortin I)	ANXA2	302	ENSG00000182718	pseudogenes ANX2P1 on 4q21-q31; ANX2P2 on 9p13; ANX2P3 on 10q24-q22		Anxa2 (MGI:88246)			
chr15	60419608	60479159	15q21.3	15q22.2		610835	NARG2	NMDA receptor-regulated 2	ICE2	79664	ENSG00000128915	pseudogenes on chr.4 and chr.3		Ice2 (MGI:2135947)			
chr15	60488283	61229302	15q21-q22	15q22.2		600825	RORA	RAR-related orphan receptor A	RORA	6095	ENSG00000069667			Rora (MGI:104661)			
chr15	61852388	62060464	15q22.1	15q22.2		608879	"VPS13C, KIAA1421, PARK23"	"Vacuolar protein sorting 13, yeast, homolog of, C"	VPS13C	54832	ENSG00000129003		"Parkinson disease 23, autosomal recessive, early onset, 616840 (3), Autosomal recessive"	Vps13c (MGI:2444207)			
chr15	62066976	62070916	15q21.3	15q22.2		610343	"C2CD4A, NLF1"	C2 calcium-dependent domain containing 4A	C2CD4A	145741	ENSG00000198535			C2cd4a (MGI:3645763)			
chr15	62163534	62165731	15q21.3	15q22.2		610344	"C2CD4B, NLF2"	C2 calcium-dependent domain containing 4B	C2CD4B	388125	ENSG00000205502			C2cd4b (MGI:1922947)			
chr15	62390522	62844630	15q22.2	15q22.2		607349	"TLN2, KIAA0320"	Talin 2	TLN2	83660	ENSG00000171914			Tln2 (MGI:1917799)			
chr15	62823956	62824040	15q22.2	15q22.2		615845	MIR190A	Micro RNA 190A	MIR190A	406965							
chr15	63042638	63071914	15q22.1	15q22.2		191010	"TPM1, CMH3, CMD1Y , LVNC9"	"Tropomyosin 1, alpha"	TPM1	7168	ENSG00000140416		"Cardiomyopathy, dilated, 1Y, 611878 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 3, 115196 (3), Autosomal dominant; Left ventricular noncompaction 9, 611878 (3), Autosomal dominant"				
chr15	63121799	63142064	15q22.1	15q22.2		608440	LACTB	"Lactamase, beta"	LACTB	114294	ENSG00000103642			Lactb (MGI:1933395)			
chr15	63153339	63157541	15q22.2	15q22.2		612055	RPS27L	Ribosomal protein S27-like	RPS27L	51065	ENSG00000185088			Rps27l (MGI:1915191)			
chr15	63189528	63267775	15q22.2	15q22.2		613532	RAB8B	Ras-associated protein RAB8B	RAB8B	51762	ENSG00000166128			Rab8b (MGI:2442982)			
chr15	63277549	63309125	15q22.2	15q22.2		607630	APH1B	"Anterior pharynx defective 1, C. elegans, homolog of, B"	APH1B	83464	ENSG00000138613			Aph1b (MGI:3522097)			
chr15	63321377	63382165	15q22	15q22.2		603263	CA12	Carbonic anhydrase XII	CA12	771	ENSG00000074410		"Hyperchlorhidrosis, isolated, 143860 (3), Autosomal recessive"	Car12 (MGI:1923709)			
chr15	63504510	63594639	15q22.3	15q22.31		604728	USP3	Ubiquitin-specific protease 3	USP3	9960	ENSG00000140455			Usp3 (MGI:2152450)			
chr15	63594793	63603431	15q22.1	15q22.31		609088	"FBXL22, FBL22"	F-box and leucine-rich repeat protein 22	FBXL22	283807	ENSG00000197361						
chr15	63608617	63833947	15q22.31	15q22.31		605109	"HERC1, MDFPMR"	HECT domain and RCC1-like domain 1	HERC1	8925	ENSG00000103657		"Macrocephaly, dysmorphic facies, and psychomotor retardation, 617011 (3), Autosomal recessive"	Herc1 (MGI:2384589)			
chr15	63907035	64046469	15q22.31	15q22.31		616567	"DAPK2, DRP1"	Death-associated protein kinase 2	DAPK2	23604	ENSG00000035664			Dapk2 (MGI:1341297)			
chr15	64094065	64144233	15q22.3	15q22.31		601272	"SNX1, SNX1A"	Sorting nexin 1	SNX1	6642	ENSG00000028528			Snx1 (MGI:1928395)			
chr15	64155814	64163154	15q21-q22	15q22.31		123841	"PPIB, CYPB, OI9"	Peptidyl-prolyl isomerase B	PPIB	5479	ENSG00000166794		"Osteogenesis imperfecta, type IX, 259440 (3), Autosomal recessive"	Ppib (MGI:97750)			
chr15	64165516	64356258	15q22.1-q22.31	15q22.31		606274	CSNK1G1	"Casein kinase I, gamma-1"	CSNK1G1	53944	ENSG00000169118			Csnk1g1 (MGI:2660884)			
chr15	64364993	64387686	15q22.1	15q22.31		610696	"PAF, OEATC1, KIAA0101"	"PCNA-associated factor, 15kD"	PCLAF	9768	ENSG00000166803			Pclaf (MGI:1915276)			
chr15	64387803	64455302	15q22.31	15q22.31		604501	"TRIP4, ASC1, SMABF1, MDCDC"	Thyroid hormone receptor interactor 4	TRIP4	9325	ENSG00000103671	mutation identified in 1 MDCDC family	"?Muscular dystrophy, congenital, Davignon-Chauveau type, 617066 (3), Autosomal recessive; Spinal muscular atrophy with congenital bone fractures 1, 616866 (3), Autosomal recessive"	Trip4 (MGI:1928469)			
chr15	64460349	64686067	15q22.31	15q22.31		617474	"ZNF609, KIAA0295"	Zinc finger ptoein 609	ZNF609	23060	ENSG00000180357			Zfp609 (MGI:2674092)			
chr15	64687573	64703280	15q22.31	15q22.31		604152	OAZ2	Ornithine decarboxylase antizyme 2	OAZ2	4947	ENSG00000180304			Oaz2 (MGI:109492)			
chr15	64815629	64827172	15q22.31	15q22.31		610953	"PIF1, PIF"	"Pif1, S. cerevisiae, homolog of"	PIF1	80119	ENSG00000140451			Pif1 (MGI:2143057)			
chr15	64963020	64989945	15q21-q22	15q22.31		608181	"ACP33, MAST, SPG21"	"Acidic cluster protein, 33kD, (maspardin)"	SPG21	51324	ENSG00000090487		"Mast syndrome, 248900 (3), Autosomal recessive"	Spg21 (MGI:106403)			
chr15	65001511	65029638	15q22.31	15q22.31		611766	"MTFMT, COXPD15"	Mitochondrial methionyl-tRNA formyltransferase	MTFMT	123263	ENSG00000103707		"Combined oxidative phosphorylation deficiency 15, 614947 (3), Autosomal recessive"	Mtfmt (MGI:1916856)			
chr15	65045369	65053396	15q21	15q22.31		612085	OSTB	"Organic solute transporter, beta"	SLC51B	123264	ENSG00000186198			Slc51b (MGI:3582052)			
chr15	65076815	65079937	15q22.31	15q22.31		613727	"KBTBD13, NEM6"	Kelch repeat and BTB/POZ domains-containing protein 13	KBTBD13	390594	ENSG00000234438		"Nemaline myopathy 6, autosomal dominant, 609273 (3), Autosomal dominant"	Kbtbd13 (MGI:1921742)			
chr15	65117378	65133835	15q22.31	15q22.31		608138	PDCD7	Programmed cell death 7	PDCD7	10081	ENSG00000090470			Pdcd7 (MGI:1859170)			
chr15	65148218	65185419	15q22.31	15q22.31		615611	CLPX	Caseinolytic mitochondrial matrix peptidase chaperone subunit	CLPX	10845	ENSG00000166855			Clpx (MGI:1346017)			
chr15	65195998	65213141	15q22	15q22.31		603489	CILP	Cartilage intermediate layer protein	CILP	8483			"{Lumbar disc disease, susceptibility to}, 603932 (3)"	Cilp (MGI:2444507)			
chr15	65296050	65296166	15q22.31	15q22.31		180691	"RNU5A, RNU5"	"RNA, U5A small nuclear"	RNU5A-1	26831							
chr15	65327126	65378039	15q22.3-q23	15q22.31		604184	PUNC	Putative neuronal cell adhesion molecule	IGDCC3	9543	ENSG00000174498			Igdcc3 (MGI:1202390)			
chr15	65381483	65423071	15q22.31	15q22.31		616810	"IGDCC4, NOPE, KIAA1628"	"Immunoglobulin superfamily, DCC subclass, member 4"	IGDCC4	57722	ENSG00000103742			Igdcc4 (MGI:1858497)			
chr15	65442462	65517712	15q22	15q22.31		606819	DPP8	Dipeptidyl peptidase 8	DPP8	54878	ENSG00000074603			Dpp8 (MGI:1921638)			
chr15	65530488	65578354	15q22.31	15q22.31		615940	"PTPLAD1, BIND1, HACD3"	Protein tyrosine phosphatase-like A domain-containing protein 1	HACD3	51495	ENSG00000074696			Hacd3 (MGI:1889341)			
chr15	65611312	65660994	15q22	15q22.31		603617	"SLC24A1, NCKX1, CSNB1D"	"Solute carrier family 24 (sodium/potassium/calcium exchanger), member 1"	SLC24A1	9187	ENSG00000074621		"Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830 (3), Autosomal recessive"	Slc24a1 (MGI:2384871)			
chr15	65655233	65792292	15q22.31	15q22.31		600382	DENND4A	DENN/MADD domain containing 4A	DENND4A	10260	ENSG00000174485			Dennd4a (MGI:2142979)			
chr15	65869458	65891990	15q21.3-q22.31	15q22.31		605570	RAB11A	"Ras family, member RAB11A"	RAB11A	8766	ENSG00000103769			Rab11a (MGI:1858202)			
chr15	65889716	66253736	15q22.31	15q22.31		612454	"MEGF11, KIAA1781"	Multiple epidermal growth factor-like domains 11	MEGF11	84465	ENSG00000157890			Megf11 (MGI:1920951)			
chr15	66293256	66333897	15q22.31	15q22.31		614183	"DIS3L, DIS3L1, KIAA1955"	"Dis3 mitotic control, S. cerevisiae, homolog-like"	DIS3L	115752	ENSG00000166938			Dis3l (MGI:2143272)			
chr15	66334973	66387272	15q22.3	15q22.31		610716	TIPIN	Timeless-interacting protein	TIPIN	54962	ENSG00000075131			Tipin (MGI:1921571)			
chr15	66386872	66491543	15q21	15q22.31		176872	"MAP2K1, PRKMK1, MKK1, MEK1, CFC3"	Mitogen-activated protein kinase kinase 1	MAP2K1	5604	ENSG00000169032	pseudogene on 8p21	"Cardiofaciocutaneous syndrome 3, 615279 (3)"	Map2k1 (MGI:1346866)			
chr15	66489747	66497814	15q22.31	15q22.31		605979	"SNAPC5, SNAP19"	"Small nuclear RNA-activating protein complex, polypeptide 5"	SNAPC5	10302	ENSG00000174446			Snapc5 (MGI:1914282)			
chr15	66499314	66504854	15q	15q22.31		180479	RPL4	Ribosomal protein L4	RPL4	6124	ENSG00000174444			Rpl4 (MGI:1915141)			
chr15	66505082	66549484	15q22.3	15q22.31		609984	ZWILCH	"Zwilch, Drosophila, homolog of"	ZWILCH	55055	ENSG00000174442			Zwilch (MGI:1915264)			
chr15	66547467	66565978	15q22.31	15q22.31		617060	"LCTL, KLG, KLPH"	Lactase-like protein	LCTL	197021	ENSG00000188501			Lctl (MGI:2183549)			
chr15	66702109	66781999	15q21-q22	15q22.31		602931	"SMAD6, MADH6, AOVD2"	"Mothers against decapentaplegic, Drosophila, homolog of, 6"	SMAD6	4091	ENSG00000137834		"Aortic valve disease 2, 614823 (3), Autosomal dominant; {Craniosynostosis 7, susceptibility to}, 617439 (3), Autosomal dominant"	Smad6 (MGI:1336883)			
chr15	66900000	67000000	15q22.32			612579	STQTL16	Stature quantitative trait locus 16		100270802		associated with rs8038652	"{Stature QTL 16}, 612579 (2)"				
chr15	67065856	67195194	15q22.3	15q22.33		603109	"SMAD3, MADH3, LDS3"	"Mothers against decapentaplegic, Drosophila, homolog of, 3"	SMAD3	4088	ENSG00000166949		"Loeys-Dietz syndrome 3, 613795 (3), Autosomal dominant"	Smad3 (MGI:1201674)			
chr15	67200000	101991189	15q23-q26.3			607248	GLM4	Glioma susceptibility 4		338030		max lod at D15S130	"{Glioma susceptibility 4}, 607248 (2)"				
chr15	67200674	67255197	15q22.33-q23	15q23		614888	"AAGAB, p34, PPKP1A, PPKP1, KPPP1"	Alpha- and gamma-adaptin-binding protein	AAGAB	79719	ENSG00000103591		"Keratoderma, palmoplantar, punctate type IA, 148600 (3), Autosomal dominant"	Aagab (MGI:1914189)			
chr15	67254771	67501803	15q22.31	15q23		612523	"IQCH, NYDSP5"	IQ motif-containing protein H	IQCH	64799	ENSG00000103599			Iqch (MGI:1925500)			
chr15	67542682	67807116	15q23	15q23		602520	"MAP2K5, PRKMK5, MEK5, MAPKK5"	Mitogen-activated protein kinase kinase 5	MAP2K5	5607	ENSG00000137764			Map2k5 (MGI:1346345)			
chr15	67819703	67834560	15q23	15q23		611273	"LBXCOR1, CORL1"	"LBX1 corepressor 1, mouse, homolog of"	SKOR1	390598	ENSG00000188779						
chr15	67839939	67840044	15q23	15q23		180692	"RNU6-1, RNU6A, RNU6"	"RNA, U6 small nuclear 1"	RNU6-1	26827							
chr15	68054178	68191463	15q22	15q23		603566	"PIAS1, DDXBP1, GBP"	"protein inhibitor of activated STAT, 1"	PIAS1	8554	ENSG00000033800			Pias1 (MGI:1913125)			
chr15	68206991	68229741	15q21-q23	15q23		606725	"CLN6, CLN4A"	CLN6 gene	CLN6	54982	ENSG00000128973		"Ceroid lipofuscinosis, neuronal, 6, 601780 (3), Autosomal recessive; Ceroid lipofuscinosis, neuronal, Kufs type, adult onset, 204300 (3), Autosomal recessive"	Cln6 (MGI:2159324)			
chr15	68277802	68295864	15q23	15q23		613539	"FEM1B, KIAA0396"	"Fem1, C. elegans, homolog of, B"	FEM1B	10116	ENSG00000169018			Fem1b (MGI:1335087)			
chr15	68297432	68432311	15q23	15q23		604789	ITGA11	"Integrin, alpha-11"	ITGA11	22801	ENSG00000137809			Itga11 (MGI:2442114)			
chr15	68518372	68727805	15q23	15q23		605002	"CORO2B, CLIPINC"	Coronin 2B	CORO2B	10391	ENSG00000103647			Coro2b (MGI:2444283)			
chr15	68778534	68820921	15q22.3-q23	15q23		600832	"ANP32A, PHAP1"	"Acidic (leucine-rich) nuclear phosphoprotein 32 family, member A"	ANP32A	8125	ENSG00000140350						
chr15	68930499	69057160	15q23	15q23		606572	NOX5	NADPH oxidase 5	NOX5	79400	ENSG00000255346						
chr15	68930499	68946810	15q22	15q23		609399	SPESP1	Sperm equatorial segment protein 1	SPESP1	246777	ENSG00000258484			Spesp1 (MGI:1913962)			
chr15	69080849	69095823	15q23	15q23		616492	"EWSAT1, LINC00277"	"Ewing sarcoma-associated transcript 1, noncoding"	EWSAT1	283673							
chr15	69160554	69272208	15q23	15q23		612134	"GLCE, HSEPI, KIAA0836"	Glucuronic acid epimerase	GLCE	26035	ENSG00000138604			Glce (MGI:2136405)			
chr15	69284133	69407636	15q23	15q23		607781	"PAQR5, MPRG"	"Progestin and ADIPOQ receptor family, member 5"	PAQR5	54852	ENSG00000137819			Paqr5 (MGI:1921340)			
chr15	69414245	69448426	15q23	15q23		605064	"KIF23, KNSL5, MKLP1"	Kinesin family member 23	KIF23	9493	ENSG00000137807			Kif23 (MGI:1919069)			
chr15	69452819	69455544	Chr.15	15q23		180520	RPLP1	"Ribosomal phosphoprotein, Large, P1"	RPLP1	6176	ENSG00000137818						
chr15	69561719	69571439	15q23	15q23		616387	DRAIC	"Downregulated RNA in androgen-independent cells, noncoding"	DRAIC	145837							
chr15	69592199	69695749	15q23	15q23		616273	PCAT29	"Prostate cancer-associated transcript 29, noncoding"	PCAT29	104472713							
chr15	70047789	70098170	15q22	15q23		600190	"TLE3, ESG"	"Transducin-like enhancer of split 3, homolog of Drosophila a E(spl)"	TLE3	7090	ENSG00000140332			Tle3 (MGI:104634)			
chr15	70654553	70778822	15q24	15q23		612516	"UACA, NUCLING"	Uveal autoantigen with coiled-coil domains and ankyrin repeats	UACA	55075	ENSG00000137831			Uaca (MGI:1919815)			
chr15	70831523	70854264	15q23	15q23		611300	"LARP6, ACHN"	"La ribonucleoprotein domain family, member 6"	LARP6	55323	ENSG00000166173			Larp6 (MGI:1914807)			
chr15	70881341	70892432	15q23	15q23		612538	THAP10	THAP domain-containing protein 10	THAP10	56906	ENSG00000129028						
chr15	71115615	71783382	15q23	15q23		614476	"THSD4, ADAMTSL6"	Thrombospondin type-1 domain-containing 4	THSD4	79875	ENSG00000187720			Thsd4 (MGI:2672033)			
chr15	71810547	71818258	15q23	15q23		604485	"NR2E3, PNR, ESCS, RP37"	"Nuclear receptor subfamily 2, group E, member 3"	NR2E3	10002	ENSG00000278570	near BBS4	"Enhanced S-cone syndrome, 268100 (3), Autosomal recessive; Retinitis pigmentosa 37, 611131 (3), Autosomal recessive, Autosomal dominant"	Nr2e3 (MGI:1346317)			
chr15	71822290	72118576	15q22-q23	15q23		604875	MYO9A	Myosin IXa	MYO9A	4649	ENSG00000066933			Myo9a (MGI:107735)			
chr15	72114257	72143687	15q23	15q23		608659	"SENP8, NEDP1, DEN1"	"Sentrin-specific protease family, member 8"	SENP8	123228	ENSG00000166192			Senp8 (MGI:1918849)			
chr15	72199028	72231623	15q22	15q23		179050	"PKM, PKM2, PK3, THBP1"	"Pyruvate kinase, muscle"	PKM	5315	ENSG00000067225			Pkm (MGI:97591)			
chr15	72284726	72320183	15q24	15q23		612681	"CELF6, BRUNOL6"	"CUGbp- and ELAV-like family, member 6"	CELF6	60677	ENSG00000140488						
chr15	72343434	72376472	15q23-q24	15q23		606869	"HEXA, TSD"	"Hexosaminidase A, alpha polypeptide"	HEXA	3073	ENSG00000213614	on 15q+ in APL	"GM2-gangliosidosis, several forms, 272800 (3), Autosomal recessive; [Hex A pseudodeficiency], 272800 (3), Autosomal recessive; Tay-Sachs disease, 272800 (3), Autosomal recessive"	Hexa (MGI:96073)			
chr15	72400000	88500000	15q24-q25			612274	CILD8	"Ciliary dyskinesia, primary, 8"		100190786		max lod at D15S154	"Ciliary dyskinesia, primary, 8, 612274 (2)"				
chr15	72400000	78000000	15q24			603204	ENFL2	"Epilepsy, nocturnal frontal lobe, type 2"		50971		some ENFL not on 20q or 15q	"Epilepsy, nocturnal frontal lobe, type 2, 603204 (2), Autosomal dominant"				
chr15	72400000	78000000	15q24			602685	MRST	"Mental retardation, severe, with spasticity and tapetoretinal degeneration"		8126			"Mental retardation, severe, with spasticity and tapetoretinal degeneration, 602685 (2)"				
chr15	72474325	72586554	15q24	15q24.1		605624	"ARIH1, ARI, UBCH7BP"	"Ariadne, Drosophila, homolog of, 1"	ARIH1	25820	ENSG00000166233			Arih1 (MGI:1344363)			
chr15	72686178	72738475	15q22.3-q23	15q24.1		600374	BBS4	BBS4 gene	BBS4	585	ENSG00000140463		"Bardet-Biedl syndrome 4, 615982 (3), Autosomal recessive"	Bbs4 (MGI:2143311)			
chr15	72751366	72783784	15q24.1	15q24.1		611861	ADPGK	ADP-dependent glucokinase	ADPGK	83440	ENSG00000159322			Adpgk (MGI:1919391)			
chr15	73051714	73305205	15q22.3-q23	15q24.1		601907	"NEO1, NGN"	"Neogenin, chicken, homolog of, 1"	NEO1	4756	ENSG00000067141			Neo1 (MGI:1097159)			
chr15	73319858	73369263	15q24-q25	15q24.1		605206	"HCN4, SSS2"	Hyperpolarization-activated cyclic nucleotide-gated potassium channel 4	HCN4	10021	ENSG00000138622		"Brugada syndrome 8, 613123 (3); Sick sinus syndrome 2, 163800 (3), Autosomal dominant"	Hcn4 (MGI:1298209)			
chr15	73560002	73633411	15q24.1	15q24.1		612820	"NPTN, SDFR1, GP55, NP55, GP65, NP65"	Neuroplastin	NPTN	27020	ENSG00000156642						
chr15	73566937	73569542	15q24.1	15q24.1		615176	NPTNIT1	"NPTN intronic transcript 1, noncoding"	NPTN-IT1	101241892							
chr15	73683965	73714517	15q23-q24	15q24.1		605715	"CD276, B7H3"	CD276 molecule	CD276	80381	ENSG00000103855			Cd276 (MGI:2183926)			
chr15	73735430	73753169	15q24.1	15q24.1		617128	"C15orf59, INSYN1"	Chromosome 15 open reading frame 59	C15orf59	388135	ENSG00000205363			6030419C18Rik (MGI:2442108)			
chr15	73917467	73928247	15q24.1	15q24.1		616800	LOXL1AS1	LOXL1 antisense RNA 1	LOXL1-AS1	100287616							
chr15	73926457	73952140	15q24.1	15q24.1		153456	"LOXL1, LOXL"	Lysyl oxidase-like 1	LOXL1	4016	ENSG00000129038		"{Exfoliation syndrome, susceptibility to}, 177650 (3), Autosomal dominant"	Loxl1 (MGI:106096)			
chr15	73983217	73994635	15q22	15q24.1		608326	"STOML1, STORP"	Stomatin-like protein 1	STOML1	9399	ENSG00000067221			Stoml1 (MGI:1916356)			
chr15	73994672	74047818	15q22	15q24.1		102578	"PML, MYL"	"Promyelocytic leukemia, inducer of"	PML	5371	ENSG00000140464	fused with RARA in APL	"Leukemia, acute promyelocytic, PML/RARA type (3)"	Pml (MGI:104662)			
chr15	74069856	74082549	15q22	15q24.1		610288	"GOLGA6, GLP"	"Golgi autoantigen, golgin subfamily A, 6"	GOLGA6A	342096	ENSG00000159289						
chr15	74100313	74141825	15q24.1	15q24.1		614179	"ISLR2, LINX, KIAA1464"	Immunoglobulin superfamily containing leucine-rich repeat 2	ISLR2	57611	ENSG00000167178			Islr2 (MGI:2444277)			
chr15	74173745	74176870	15q23-q24	15q24.1		602059	ISLR	Immunoglobulin superfamily containing leucine-rich repeat	ISLR	3671	ENSG00000129009			Islr (MGI:1349645)			
chr15	74179465	74212266	15q24.1	15q24.1		610745	"STRA6, MCOPS9, MCOPCB8"	"Stimulated by retinoic acid 6, mouse, homolog of"	STRA6	64220	ENSG00000137868		"Microphthalmia, isolated, with coloboma 8, 601186 (3), Autosomal recessive; Microphthalmia, syndromic 9, 601186 (3), Autosomal recessive"	Stra6 (MGI:107742)			
chr15	74337761	74367739	15q24.1	15q24.1		118485	"CYP11A1, P450SCC"	"Cytochrome P450, subfamily XIA, polypeptide 1 (cholesterol side chain cleavage enzyme)"	CYP11A1	1583	ENSG00000140459		"Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3)"	Cyp11a1 (MGI:88582)			
chr15	74409283	74433958	15q24.1	15q24.1		607961	"SEMA7A, SEMAL, SEMAK1, CDW108, JMH"	Semaphorin 7A	SEMA7A	8482	ENSG00000138623		"[Blood group, John-Milton-Hagen system], 614745 (3)"	Sema7a (MGI:1306826)			
chr15	74445976	74461828	15q22.3-q23	15q24.1		609748	UBL7	Ubiquitin-like 7	UBL7	84993	ENSG00000138629			Ubl7 (MGI:1916709)			
chr15	74541176	74598130	15q24	15q24.1		612457	"ARID3B, DRIL2, BDP"	AT-rich interactive domain-containing protein 3B	ARID3B	10620	ENSG00000179361			Arid3b (MGI:1930768)			
chr15	74598475	74645417	15q24	15q24.1		602990	CLK3	CDC-like kinase 3	CLK3	1198	ENSG00000179335			Clk3 (MGI:1098670)			
chr15	74630557	74696433	15q24.1	15q24.1		609842	"EDC3, YJDC, MRT50"	"Enhancer of mRNA decapping 3, S. cerevisiae, homolog of"	EDC3	80153	ENSG00000179151	mutation identified in 1 MRT50 family	"?Mental retardation, autosomal recessive 50, 616460 (3), Autosomal recessive"	Edc3 (MGI:2142951)			
chr15	74719541	74725609	15q24.1	15q24.1		108330	"CYP1A1, CYP1"	"Cytochrome P450, subfamily I, aromatic compound-inducible, polypeptide 1"	CYP1A1	1543	ENSG00000140465	head-to-head with CYP1A2		Cyp1a1 (MGI:88588)			
chr15	74748842	74756599	15q24.1	15q24.1		124060	CYP1A2	"Cytochrome P450, subfamily I, aromatic compound-inducible, polypeptide 2"	CYP1A2	1544	ENSG00000140505	23.3kb from CYP1A1		Cyp1a2 (MGI:88589)			
chr15	74782083	74803197	15q23-q25	15q24.1		124095	CSK	c-src tyrosine kinase	CSK	1445	ENSG00000103653			Csk (MGI:88537)			
chr15	74836115	74843210	15q24.1	15q24.1		613472	ULK3	UNC51-like kinase 3	ULK3	25989	ENSG00000140474			Ulk3 (MGI:1918992)			
chr15	74843729	74873378	Chr.15	15q24.1		606912	SCAMP2	Secretory carrier membrane protein 2	SCAMP2	10066	ENSG00000140497			Scamp2 (MGI:1346518)			
chr15	74890004	74899456	15q22-qter	15q24.1		154550	"MPI, PMI1, CDG1B"	Mannosephosphate isomerase (phosphomannose isomerase 1)	MPI	4351	ENSG00000178802		"Congenital disorder of glycosylation, type Ib, 602579 (3), Autosomal recessive"	Mpi (MGI:97075)			
chr15	74920274	74938153	15q25	15q24.2		603773	COX5A	"Cytochrome C oxidase, subunit Va"	COX5A	9377	ENSG00000178741	pseudogene on 14q22		Cox5a (MGI:88474)			
chr15	74995534	75021494	15q23	15q24.2		613766	SCAMP5	Secretory carrier membrane protein 5	SCAMP5	192683	ENSG00000198794			Scamp5 (MGI:1928948)			
chr15	75023543	75060179	15q24.2	15q24.2		609854	PPCDC	Phosphopantothenoylcysteine decarboxylase	PPCDC	60490	ENSG00000138621			Ppcdc (MGI:1914062)			
chr15	75335995	75341926	15q24.2	15q24.2		616701	COMMD4	COMM domain-containing protein 4	COMMD4	54939	ENSG00000140365			Commd4 (MGI:1913449)			
chr15	75346637	75355250	15q24.2	15q24.2		608844	"NEIL1, NEI1, FPG1"	Endonuclease VIII-like 1	NEIL1	79661	ENSG00000140398			Neil1 (MGI:1920024)			
chr15	75354325	75368679	15q11-q13	15q24.2		154580	"MAN2C1, MANA"	"Mannosidase, alpha, class 2C, member 1"	MAN2C1	4123	ENSG00000140400			Man2c1 (MGI:1920994)			
chr15	75369378	75455818	15q24	15q24.2		607776	"SIN3A, WITKOS"	"Sin3, yeast, homolog of, A"	SIN3A	25942	ENSG00000169375		"Witteveen-Kolk syndrome, 613406 (3), Autosomal dominant"	Sin3a (MGI:107157)			
chr15	75467120	75579290	15q24.2	15q24.2		600768	PTPN9	"Protein-tyrosine phosphatase, nonreceptor-type, 9"	PTPN9	5780	ENSG00000169410			Ptpn9 (MGI:1928376)			
chr15	75639084	75640322	15q24	15q24.2		612980	"IMP3, MRPS4, BRMS2"	"Imp3, S. cerevisiae, homolog of"	IMP3	55272	ENSG00000177971			Imp3 (MGI:1916119)			
chr15	75674321	75712847	15q24.2	15q24.2		601172	"CSPG4, MCSPG, MSK16, NG2"	Chondroitin sulfate proteoglycan	CSPG4	1464	ENSG00000173546			Cspg4 (MGI:2153093)			
chr15	75843285	75901046	15q23	15q24.2		612501	"UBE2Q2, LOC92912"	Ubiquitin-conjugating enzyme E2Q 2	UBE2Q2	92912	ENSG00000140367			Ube2q2 (MGI:2388672)			
chr15	75903858	75935267	15q23	15q24.2		609096	"FBXO22, FBX22"	F-box only protein 22	FBXO22	26263	ENSG00000167196			Fbxo22 (MGI:1926014)			
chr15	75933218	76069829	15q24.1	15q24.2		610894	"NRG4, HRG4"	Neuregulin 4	NRG4	145957	ENSG00000169752			Nrg4 (MGI:1933833)			
chr15	76216227	76311468	15q23-q25	15q24.2-q24.3		608053	"ETFA, GA2, MADD"	"Electron transfer flavoprotein, alpha polypeptide"	ETFA	2108	ENSG00000140374		"Glutaric acidemia IIA, 231680 (3), Autosomal recessive"	Etfa (MGI:106092)			
chr15	76348184	76905456	15q24	15q24.3		611611	"SCAPER, KIAA1454"	S-phase cyclin A-associated protein in the endoplasmic reticulum	SCAPER	49855	ENSG00000140386			Scaper (MGI:1925976)			
chr15	76931620	76950259	15q23	15q24.3		602584	"RCN2, ERC55"	"Reticulocalbin 2, EF-hand calcium binding domain (endoplasmic reticulum calcium-binding protein, 55kD)"	RCN2	5955	ENSG00000117906			Rcn2 (MGI:1349765)			
chr15	76994679	77037474	15q24-q25.1	15q24.3		606347	"PSTPIP1, PSTPIP, CD2BP1, PAPAS"	Proline-serine-threonine phosphatase-interacting protein 1	PSTPIP1	9051	ENSG00000140368		"Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, 604416 (3), Autosomal dominant"	Pstpip1 (MGI:1321396)			
chr15	77044016	77071227	15q24.3	15q24.3		613134	TSPAN3	Tetraspanin 3	TSPAN3	10099	ENSG00000140391			Tspan3 (MGI:1928098)			
chr15	77100828	77420698	15q24.3	15q24.3		614248	"PEAK1, KIAA2002"	Pseudopodium-enriched atypical kinase 1	PEAK1	79834	ENSG00000173517			Peak1 (MGI:2442366)			
chr15	77420650	77519898	15q24	15q24.3		605534	HMG20A	High mobility group protein 20A	HMG20A	10363	ENSG00000140382			Hmg20a (MGI:1914117)			
chr15	77613023	77820899	15q24	15q24.3		609791	"LRRN6A, LERN1, LINGO1"	"Leucine-rich repeat protein, neuronal, 6A"	LINGO1	84894	ENSG00000169783			Lingo1 (MGI:1915522)			
chr15	78000000	88500000	15q25			614294	"DEL15q25, C15DELq25"	Chromosome 15q25 deletion syndrome				"chr15:82,889,423-83,552,890, NCBI36"	"Chromosome 15q25 deletion syndrome, 614294 (4), Autosomal dominant"				
chr15	78000000	101991189	15q25-q26			606451	DFNA30	"Deafness, autosomal dominant 30"	DFNA30	23719			"Deafness, autosomal dominant 30, 606451 (2), Autosomal dominant"				
chr15	78000000	93800000	15q25.1-q26.1			607728	"POROK4, DSAP2"	"Porokeratosis 4, disseminated superficial actinic"		353147		between D15S1023 and D15S1030	"Porokeratosis 4, disseminated superficial actinic, 607728 (2)"				
chr15	78104605	78131975	15q24	15q25.1		605564	"CIB2, KIP2"	Calcium- and integrin-binding protein 2	CIB2	10518	ENSG00000136425		"Deafness, autosomal recessive 48, 609439 (3), Autosomal recessive; Usher syndrome, type IJ, 614869 (3), Autosomal recessive"	Cib2 (MGI:1929293)			
chr15	78149361	78170541	15q25.1-q25.2	15q25.1		601149	IDH3A	Isocitrate dehydrogenase 3 (NAD+) alpha	IDH3A	3419	ENSG00000166411			Idh3a (MGI:1915084)			
chr15	78167467	78234706	12q23-q24	15q25.1		614362	"ACSBG1, BG, BG1, KIAA0631"	"Acyl-CoA synthetase, bubble gum family, member 1"	ACSBG1	23205	ENSG00000103740			Acsbg1 (MGI:2385656)			
chr15	78340323	78348229	15q24	15q25.1		180230	"CRABP1, RBP5"	Cellular retinoic acid-binding protein-1	CRABP1	1381	ENSG00000166426	distal to APL breakpoint		Crabp1 (MGI:88490)			
chr15	78437430	78501455	15q25.1	15q25.1		147582	IREB2	Iron-responsive element-binding protein-2	IREB2	3658	ENSG00000136381			Ireb2 (MGI:1928268)			
chr15	78507563	78537372	15q25.1	15q25.1		614681	AGPHD1	Aminoglycoside phosphotransferase domain-containing protein 1	HYKK	123688	ENSG00000188266			Hykk (MGI:2443139)			
chr15	78540404	78549261	15q25.1	15q25.1		176846	"PSMA4, PSC9, HC9"	"Proteasome subunit, alpha-type, 4"	PSMA4	5685	ENSG00000041357			Psma4 (MGI:1347060)			
chr15	78565519	78595268	15q25.1	15q25.1		118505	"CHRNA5, LNCR2"	"Cholinergic receptor, neuronal nicotinic, alpha polypeptide-5"	CHRNA5	1138	ENSG00000169684		"{Lung cancer susceptibility 2}, 612052 (3); {Nicotine dependence, susceptibility to}, 612052 (3)"	Chrna5 (MGI:87889)			
chr15	78593051	78621294	15q25.1	15q25.1		118503	"CHRNA3, LNCR2, PAOD2"	"Cholinergic receptor, neuronal nicotinic, alpha polypeptide-3"	CHRNA3	1136	ENSG00000080644		"{Lung cancer susceptibility 2}, 612052 (3)"	Chrna3 (MGI:87887)			
chr15	78623281	78655585	15q24	15q25.1		118509	CHRNB4	"Cholinergic receptor, neuronal nicotinic, beta polypeptide-4"	CHRNB4	1143	ENSG00000117971			Chrnb4 (MGI:87892)			
chr15	78759202	78811475	15q25.1	15q25.1		605009	ADAMTS7	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 7"	ADAMTS7	11173	ENSG00000136378			Adamts7 (MGI:1347346)			
chr15	78872780	78897738	15q24	15q25.1		607303	"MORF4L1, MRG15"	Mortality factor 4-like 1	MORF4L1	10933	ENSG00000185787			Morf4l1 (MGI:1096551)			
chr15	78921749	78945097	15q24-q25	15q25.1		116820	CTSH	Cathepsin H	CTSH	1512	ENSG00000103811			Ctsh (MGI:107285)			
chr15	79209787	79209870	15q25.1	15q25.1		613146	"MIR184, MIRN184, KTCNCT, EDICT"	Micro RNA 184	MIR184	406960			"EDICT syndrome, 614303 (3), Autosomal dominant"				
chr15	79843546	79897284	15q25.1	15q25.1		604197	MTHFS	"5,10-methenyltetrahydrofolate synthetase"	MTHFS	10588	ENSG00000136371			"Mthfsl,Mthfs (MGI:1340032,MGI:3780550)"			
chr15	79960889	79971300	15q24.3	15q25.1		601056	BCL2A1	BCL2-related protein A1	BCL2A1	597	ENSG00000140379			"Bcl2a1d,Bcl2a1b,Bcl2a1a (MGI:102687,MGI:1278325,MGI:1278326)"			
chr15	80059567	80138392	15q25.1	15q25.1		610183	"ZFAND6, ZA20D3, AWP1"	Zinc finger AN1 domain-containing protein 6	ZFAND6	54469	ENSG00000086666			Zfand6 (MGI:1929510)			
chr15	80152822	80186581	15q23-q25	15q25.1		613871	FAH	Fumarylacetoacetase	FAH	2184	ENSG00000103876		"Tyrosinemia, type I, 276700 (3), Autosomal recessive"	Fah (MGI:95482)			
chr15	80404349	80597936	15q24	15q25.1		606036	"ARNT2, WEDAS"	Aryl hydrocarbon receptor nuclear translocator 2	ARNT2	9915	ENSG00000172379	mutation identified in 1 WEDAS family	"?Webb-Dattani syndrome, 615926 (3), Autosomal recessive"	Arnt2 (MGI:107188)			
chr15	80779342	80951770	15q24	15q25.1		608366	KIAA1199	KIAA1199 gene	CEMIP	57214	ENSG00000103888			Cemip (MGI:2443629)			
chr15	80947325	80989877	Chr.15	15q25.1		607783	"MESDC2, MESD, BOCA, KIAA0081"	Mesoderm development candidate gene 2	MESD	23184	ENSG00000117899			Mesd (MGI:1891421)			
chr15	81000953	81004003	15q25.1	15q25.1		615466	MESDC1	Mesoderm development candidate 1	TLNRD1	59274	ENSG00000140406			Tlnrd1 (MGI:1891420)			
chr15	81196877	81312762	15q26.1	15q25.1		603035	"IL16, LCF"	Interleukin 16	IL16	3603	ENSG00000172349			Il16 (MGI:1270855)			
chr15	81312665	81324182	15q26	15q25.1		607050	STARD5	Start domain-containing protein 5	STARD5	80765	ENSG00000172345			Stard5 (MGI:2156765)			
chr15	81331104	81374155	15q25.1	15q25.1		617196	TMC3	Transmembrane channel-like protein 3	TMC3	342125	ENSG00000188869			Tmc3 (MGI:2669033)			
chr15	82041777	82046142	15q25.2	15q25.2		611008	"MEX3B, RKHD3"	"Mex-3, C. elegans, homolog of, B"	MEX3B	84206	ENSG00000183496			Mex3b (MGI:1918252)			
chr15	82130219	82262762	15q25.2	15q25.2		617538	"EFL1, RIA1, EFTUD1, FAM42A"	Elongation factor-like GTPase 1	EFL1	79631	ENSG00000140598			Efl1 (MGI:2141969)			
chr15	82536749	82540563	15q	15q25.2		180472	"RPS17, RPS17L1, RPS17L2, DBA4"	Ribosomal protein S17	RPS17	6218	ENSG00000182774	previously on chr.11; pseudogenes on 5q33-qter and 17q	"Diamond-Blackfan anemia 4, 612527 (3), Autosomal dominant"	Rps17 (MGI:1309526)			
chr15	82543200	82648015	15q25.2	15q25.2		607342	CPEB1	Cytoplasmic polyadenylation element-binding protein 1	CPEB1	64506	ENSG00000214575			Cpeb1 (MGI:108442)			
chr15	82659280	82709907	15q25.2	15q25.2		602166	"AP3B2, NAPTB, EIEE48"	"Adaptor-related protein complex 3, beta 2 subunit"	AP3B2	8120	ENSG00000103723		"Epileptic encephalopathy, early infantile, 48, 617276 (3), Autosomal recessive"	Ap3b2 (MGI:1100869)			
chr15	82755944	82756070	15q25.2	15q25.2		612675	"SCARNA15, ACA45"	Small cajal body-specific RNA 15	SCARNA15	677778							
chr15	82809627	82834860	15q25.2	15q25.2		612393	"WHAMM, KIAA1971"	"Was protein homolog associated with actin, golgi membranes, and microtubules"	WHAMM	123720	ENSG00000156232			Whamm (MGI:2142282)			
chr15	82836945	82986175	15q24.3	15q25.2		604799	"HOMER2, HOMER2B, HOMER2A, DFNA68"	"Homer, homolog 2 (Drosophila)"	HOMER2	9455	ENSG00000103942	mutation identified in 1 DFNA68 family	"?Deafness, autosomal dominant 68, 616707 (3), Autosomal dominant"	Homer2 (MGI:1347354)			
chr15	82986202	82991056	15q25.2	15q25.2		614547	"FAM103A1, RAM"	"Family with sequence similarity 103, member A1"	RAMMET	83640	ENSG00000169612			Fam103a1 (MGI:1914398)			
chr15	83107485	83145402	15q24-q26	15q25.2		606562	TM6SF1	"Transmembrane 6 superfamily, member 1"	TM6SF1	53346	ENSG00000136404			Tm6sf1 (MGI:1933209)			
chr15	83112737	83208017	15q25	15q25.2		616643	"HRP3, HDGFRP3"	Hepatoma-derived growth factor-related protein 3	HDGFL3	50810	ENSG00000166503			Hdgfl3 (MGI:1352760)			
chr15	83255883	83284715	15q25.1	15q25.2		601930	BNC1	Basonuclin	BNC1	646	ENSG00000169594			Bnc1 (MGI:1097164)			
chr15	83447122	83618742	15q24	15q25.2		603362	SH3GL3	SH3-domain GRB2-like 3	SH3GL3	6457	ENSG00000140600			Sh3gl3 (MGI:700011)			
chr15	83654085	84039841	15q25.2	15q25.2		609199	"ADAMTSL3, KIAA1233"	ADAMTS-like protein 3	ADAMTSL3	57188	ENSG00000156218			Adamtsl3 (MGI:3028499)			
chr15	84631459	84642462	15q25.2	15q25.2		610417	SCAND2	SCAN domain-containing 2	SCAND2P	54581							
chr15	84641494	84654342	15q25.2	15q25.2		616144	"WDR73, HSPC264, GAMOS1"	WD repeat-containing protein 73	WDR73	84942	ENSG00000177082		"Galloway-Mowat syndrome 1, 251300 (3), Autosomal recessive"	Wdr73 (MGI:1919218)			
chr15	84655128	84658610	15q22-qter	15q25.2		162340	NMB	Neuromedin B	NMB	4828	ENSG00000197696			Nmb (MGI:1915289)			
chr15	84700000	93800000	15q25.3-q26.1			609893	"CHNG3, RTSH"	"Hypothyroidism, congenital, nongoitrous, 3"		780915		max lod at D15S655	"Hypothyroidism, congenital, nongoitrous, 3, 609893 (2)"				
chr15	84700000	98000000	15q25.3-q26.2			608691	MDD2	Major depressive disorder 2		431709			"Major depressive disorder 2, 608516 (2)"				
chr15	84748555	84806431	15q25.3	15q25.3		613624	"ZNF592, KIAA0211"	Zinc finger protein 592	ZNF592	9640	ENSG00000166716			Zfp592 (MGI:2443541)			
chr15	84816679	84873481	15q25.2	15q25.3		617608	"ALPK3, MIDORI, KIAA1330"	Alpha kinase 3	ALPK3	57538	ENSG00000136383			Alpk3 (MGI:2151224)			
chr15	84884349	84975648	15q25-q26	15q25.3		606207	"SLC28A1, CNT1"	"Solute carrier family 28 (sodium-coupled nucleoside transporter), member 1"	SLC28A1	9154	ENSG00000156222			Slc28a1 (MGI:3605073)			
chr15	84980512	85139144	15q25.3-q26.1	15q25.3		602972	PDE8A	Phosphodiesterase 8A	PDE8A	5151	ENSG00000073417			Pde8a (MGI:1277116)			
chr15	85380615	85749357	15q24-q25	15q25.3		604686	"AKAP13, HT31, LBC, BRX"	A-kinase anchor protein 13	AKAP13	11214	ENSG00000170776			Akap13 (MGI:2676556)			
chr15	86079638	87031475	15q25.3	15q25.3		615496	"AGBL1, CCP4, FECD8"	ATP/GTP-binding protein-like 1	AGBL1	123624	ENSG00000273540		"Corneal dystrophy, Fuchs endothelial, 8, 615523 (3), Autosomal dominant"	Agbl1 (MGI:3646469)			
chr15	87859748	88256795	15q25	15q25.3		191316	"NTRK3, TRKC"	"Neurotrophic tyrosine kinase, receptor, type 3"	NTRK3	4916	ENSG00000140538			Ntrk3 (MGI:97385)			
chr15	88459477	88467401	15q24-q25	15q25.3		611851	MRPL46	Mitochondrial ribosomal protein L46	MRPL46	26589	ENSG00000259494			Mrpl46 (MGI:1914558)			
chr15	88467452	88480766	15q25	15q25.3		611977	MRPS11	Mitochondrial ribosomal protein S11	MRPS11	64963	ENSG00000181991			Mrps11 (MGI:1915244)			
chr15	88500000	101991189	15q26-qter			612626	"DEL15q26qter, C15DELq26qter"	Chromosome 15q26-qter deletion syndrome				contiguous gene deletion syndrome	"Chromosome 15q26-qter deletion syndrome, 612626 (4), Isolated cases"				
chr15	88500000	93800000	15q26.1			142340	"DIH1, HCD"	"Hernia, congenital diaphragmatic 1"	DIH1	1732			"Hernia, congenital diaphragmatic 1, 142340 (2), Multifactorial"				
chr15	88500000	101991189	15q26			600318	IDDM3	Insulin-dependent diabetes mellitus-3	IDDM3	3402			"{Diabetes mellitus, insulin-dependent, 3}, 600318 (2)"				
chr15	88500000	101991189	15q26-qter			614846	LVSKS	Levy-Shanske syndrome (tetrasomy 15q26)					"Levy-Shanske syndrome, 614846 (4)"				
chr15	88500000	101991189	15q26.1-qter			166800	"OTSC1, OTS"	Otosclerosis 1	OTSC1	5012			"Otosclerosis 1, 166800 (2), Autosomal dominant"				
chr15	88500000	101991189	15q26			609289	VVS	"Syncope, familial vasovagal"		105031671			"Syncope, familial vasovagal, 609289 (2), Autosomal dominant"				
chr15	88501923	88546702	15q25.3	15q26.1		608727	DET1	"De-etiolated 1, Arabidopsis, homolog of"	DET1	55070	ENSG00000140543			Det1 (MGI:1923625)			
chr15	88604600	88632280	15q26.1	15q26.1		610177	"ISG20L1, AEN"	Interferon-stimulated exonuclease gene 20kD-like 1	AEN	64782	ENSG00000181026			Aen (MGI:1915298)			
chr15	88635613	88656343	15q26	15q26.1		604533	"ISG20, HEM45"	"Interferon-stimulated gene, 20kD"	ISG20	3669	ENSG00000172183			Isg20 (MGI:1928895)			
chr15	88803441	88875353	15q26.1	15q26.1		155760	"ACAN, AGC1, CSPG1, MSK16, SEDK, SSOAOD"	"Aggrecan (chondroitin sulfate proteoglycan-1, large aggregating proteoglycan, antigen identifies by monoclonal antibody A0122)"	ACAN	176	ENSG00000157766	mutation identified in 1 SEDK family and 1 SEMDAG family	"Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, 165800 (3), Autosomal dominant; ?Spondyloepimetaphyseal dysplasia, aggrecan type, 612813 (3), Autosomal recessive; ?Spondyloepiphyseal dysplasia, Kimberley type, 608361 (3), Autosomal dominant"				
chr15	88898682	88913468	15q25	15q26.1		602281	MFGE8	Milk fat globule-EGF factor 8	MFGE8	4240	ENSG00000140545			Mfge8 (MGI:102768)			
chr15	89088149	89202359	15q26.1	15q26.1		612196	"ABHD2, LABH2"	Abhydrolase domain-containing 2	ABHD2	11057	ENSG00000140526			Abhd2 (MGI:1914344)			
chr15	89209866	89223178	15q26	15q26.1		180090	RLBP1	"Retinaldehyde-binding protein-1, cellular"	RLBP1	6017	ENSG00000140522		"Bothnia retinal dystrophy, 607475 (3), Autosomal recessive; Fundus albipunctatus, 136880 (3), Autosomal recessive, Autosomal dominant; Newfoundland rod-cone dystrophy, 607476 (3); Retinitis punctata albescens, 136880 (3), Autosomal recessive, Autosomal dominant"	Rlbp1 (MGI:97930)			
chr15	89243953	89317131	15q25-q26	15q26.1		611360	"FANCI, KIAA1794"	FANCI gene	FANCI	55215	ENSG00000140525		"Fanconi anemia, complementation group I, 609053 (3), Autosomal recessive"	Fanci (MGI:2384790)			
chr15	89316304	89334794	15q25	15q26.1		174763	"POLG, POLG1, POLGA, PEO, SANDO, SCAE, MTDPS4A, MTDPS4B, MIRAS"	"Polymerase (DNA directed), gamma"	POLG	5428	ENSG00000140521	PEO also digenic with C10orf2	"Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700 (3), Autosomal recessive; Mitochondrial DNA depletion syndrome 4B (MNGIE type), 613662 (3), Autosomal recessive; Mitochondrial recessive ataxia syndrome (includes SANDO and SCAE), 607459 (3), Autosomal recessive; Progressive external ophthalmoplegia, autosomal dominant 1, 157640 (3), Autosomal dominant; Progressive external ophthalmoplegia, autosomal recessive 1, 258450 (3), Autosomal recessive"	Polg (MGI:1196389)			
chr15	89368016	89368105	15q26.1	15q26.1		611188	"MIR9-3, MIRN9-3"	Micro RNA 9-3	MIR9-3	407051							
chr15	89471406	89496612	15q25	15q26.1		605381	"RHCG, RHGK"	Rhesus blood group-associated kidney homolog	RHCG	51458	ENSG00000140519			Rhcg (MGI:1888517)			
chr15	89575586	89628022	15q26.1	15q26.1		613298	"C15orf42, TRESLIN"	Treslin	TICRR	90381	ENSG00000140534			Ticrr (MGI:1924261)			
chr15	89627969	89663085	15q26.1	15q26.1		611254	"KIF7, HLS2, ACLS, JBTS12, AGBK"	Kinesin family member 7	KIF7	374654	ENSG00000166813	mutation identified in 1 HLS2 family and 1 AGBK family	"Acrocallosal syndrome, 200990 (3), Autosomal recessive; ?Al-Gazali-Bakalinova syndrome, 607131 (3), Autosomal recessive; ?Hydrolethalus syndrome 2, 614120 (3), Autosomal recessive; Joubert syndrome 12, 200990 (3), Autosomal recessive"	Kif7 (MGI:1098239)			
chr15	89664364	89679416	15q26	15q26.1		170290	"PLIN1, PLIN, FPLD4"	Perilipin 1	PLIN1	5346	ENSG00000166819		"Lipodystrophy, familial partial, type 4, 613877 (3), Autosomal dominant"	Plin1 (MGI:1890505)			
chr15	89681530	89690783	15q26.1	15q26.1		603866	PEX11A	Peroxisome biogenesis factor 11A	PEX11A	8800	ENSG00000166821			Pex11a (MGI:1338788)			
chr15	89734771	89751308	15q26.1	15q26.1		608689	MESP1	Mesoderm posterior bHLH transcription factor 1	MESP1	55897	ENSG00000166823			Mesp1 (MGI:107785)			
chr15	89776357	89778753	15q26.1	15q26.1		605195	"MESP2, SCDO2"	Mesoderm posterior bHLH transcription factor 2	MESP2	145873	ENSG00000188095		"Spondylocostal dysostosis 2, autosomal recessive, 608681 (3)"	Mesp2 (MGI:1096325)			
chr15	89784894	89814851	15q25-q26	15q26.1		151530	"ANPEP, PEPN, CD13"	"Alanyl (membrane) aminopeptidase (aminopeptidase N, aminopeptidase M, microsomal aminopeptidase, CD13, p150)"	ANPEP	290	ENSG00000166825			Anpep (MGI:5000466)			
chr15	89830598	89894384	15q26.1	15q26.1		602416	AP3S2	"Adaptor-related protein complex 3, sigma-2 subunit"	AP3S2	10239	ENSG00000157823			Ap3s2 (MGI:1337060)			
chr15	89896531	89912989	15q26.1	15q26.1		615543	"C15orf38, ARPIN"	Chromosome 15 open reading frame 38	ARPIN	348110	ENSG00000242498			Arpin (MGI:1917670)			
chr15	90083977	90102553	15q26.1	15q26.1		147650	"IDH2, IDPM, D2HGA2"	"Isocitrate dehydrogenase, mitochondrial"	IDH2	3418	ENSG00000182054		"D-2-hydroxyglutaric aciduria 2, 613657 (3)"	Idh2 (MGI:96414)			
chr15	90184919	90229659	15q26.1	15q26.1		617029	SEMA4B	Semaphorin 4B	SEMA4B	10509	ENSG00000185033			Sema4b (MGI:107559)			
chr15	90230244	90265758	15q25.3-q26.1	15q26.1		602293	"CIB, KIP"	Calcium- and integrin-binding protein (kinase-interacting protein)	CIB1	10519	ENSG00000185043			Cib1 (MGI:1344418)			
chr15	90265662	90272210	15q26.1	15q26.1		616718	NGRN	Neurite outgrowth-associated protein	NGRN	51335	ENSG00000182768			Ngrn (MGI:1933212)			
chr15	90388240	90502242	15q26	15q26.1		603379	"IQGAP1, SAR1"	"RASGAP-like with IQ motifs (sar1, S. pombe, homolog of)"	IQGAP1	8826	ENSG00000140575	amplified in gastric cancer		Iqgap1 (MGI:1352757)			
chr15	90529885	90645344	15q26.1	15q26.1		608986	"CRTC3, TORC3"	CREB-regulated transcription coactivator 3	CRTC3	64784	ENSG00000140577			Crtc3 (MGI:1917711)			
chr15	90717326	90815461	15q26.1	15q26.1		604610	"RECQL3, RECQ2, BLM, BS"	"DNA helicase, RecQ-like 3"	BLM	641	ENSG00000197299		"Bloom syndrome, 210900 (3), Autosomal recessive"	Blm (MGI:1328362)			
chr15	90868591	90883457	15q25-q26	15q26.1		136950	"FURIN, PACE, FUR, PCSK3"	Furin (paired basic amino acid cleaving enzyme)	FURIN	5045	ENSG00000140564	less than 1.1kb 5' to FES		Furin (MGI:97513)			
chr15	90884420	90895775	15q26.1	15q26.1		190030	FES	"Oncogene FES, feline sarcoma virus"	FES	2242	ENSG00000182511			Fes (MGI:95514)			
chr15	90902217	90922584	15q25	15q26.1		600988	"MAN2A2, MANA2X"	"Mannosidase, alpha-, type II, isozyme X"	MAN2A2	4122	ENSG00000196547			Man2a2 (MGI:2150656)			
chr15	90930179	90954092	15q25-q26	15q26.1		611219	"UNC45A, SMAP1, GCUNC45"	"UNC45, C. elegans, homolog of, A"	UNC45A	55898	ENSG00000140553			Unc45a (MGI:2142246)			
chr15	90966037	90994650	15q26.1	15q26.1		603484	PRC1	Protein regulating cytokinesis 1	PRC1	9055	ENSG00000198901			Prc1 (MGI:1858961)			
chr15	90998415	91022838	15q26.1	15q26.1		608552	VPS33B	"Vacuolar protein sorting 33, yeast, homolog of, B"	VPS33B	26276	ENSG00000184056		"Arthrogryposis, renal dysfunction, and cholestasis 1, 208085 (3), Autosomal recessive"	Vps33b (MGI:2446237)			
chr15	91099587	91302564	15q26.1	15q26.1		185861	"SV2B, KIAA0735"	Synaptic vesicle glycoprotein 2B	SV2B	9899	ENSG00000185518			Sv2b (MGI:1927338)			
chr15	91853707	92172434	15q26	15q26.1		612435	"SLCO3A1, OATPD, OATP3A1"	"Solute carrier organic anion transporter family, member 3A1"	SLCO3A1	28232	ENSG00000176463			Slco3a1 (MGI:1351867)			
chr15	92393886	92468727	15q26	15q26.1		602546	STX	Sialyltransferase X	ST8SIA2	8128	ENSG00000140557			St8sia2 (MGI:106020)			
chr15	92900320	93028006	15q26	15q26.1		602119	"CHD2, EEOC"	Chromodomain helicase DNA binding protein-2	CHD2	1106	ENSG00000173575		"Epileptic encephalopathy, childhood-onset, 615369 (3), Autosomal dominant"	Chd2 (MGI:2448567)			
chr15	93043405	93089213	15q26.1	15q26.1		607362	RGMA	"RGM domain family, member A (repulsive guidance molecule)"	RGMA	56963	ENSG00000182175			Rgma (MGI:2679262)			
chr15	94231537	94483951	15q26.2	15q26.2		616297	MCTP2	Multiple C2 domains-containing transmembrane protein 2	MCTP2	55784	ENSG00000140563			Mctp2 (MGI:2685335)			
chr15	96325927	96340262	15q26.1-q26.2	15q26.2		107773	"NR2F2, TFCOUP2, ARP1, CHTD4"	"Nuclear receptor subfamily 2, group F, member 2 (transcription factor COUP 2)"	NR2F2	7026	ENSG00000185551		"Congenital heart defects, multiple types, 4, 615779 (3), Autosomal dominant"	Nr2f2 (MGI:1352452)			
chr15	96783406	96785614	15q26.2	15q26.2		613948	"SPATA8, SRG8"	Spermatogenesis-associated protein 8	SPATA8	145946	ENSG00000185594						
chr15	98648538	98964529	15q25-q26	15q26.3		147370	IGF1R	Insulin-like growth factor-1 receptor	IGF1R	3480	ENSG00000140443		"Insulin-like growth factor I, resistance to, 270450 (3), Autosomal recessive, Autosomal dominant"	Igf1r (MGI:96433)			
chr15	99105068	99136585	Chr.15	15q26.3		606087	DMN	Desmuslin	SYNM	23336	ENSG00000182253			Synm (MGI:2661187)			
chr15	99565546	99716487	15q26	15q26.3		600660	"MEF2A, ADCAD1"	"MADS box transcription enhancer factor 2, polypeptide A (myocyte enhancer factor 2A)"	MEF2A	4205	ENSG00000068305		"{Coronary artery disease, autosomal dominant, 1}, 608320 (3), Autosomal dominant"	Mef2a (MGI:99532)			
chr15	99971437	100342923	15q24	15q26.3		607511	"ADAMTS17, WMS4"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 17"	ADAMTS17	170691	ENSG00000140470		"Weill-Marchesani 4 syndrome, recessive, 613195 (3), Autosomal recessive"	Adamts17 (MGI:3588195)			
chr15	100400394	100544981	15q26.3	15q26.3		615276	"CERS3, LASS3, ARCI9"	Ceramide synthase 3	CERS3	204219	ENSG00000154227		"Ichthyosis, congenital, autosomal recessive 9, 615023 (3), Autosomal recessive"	Cers3 (MGI:2681008)			
chr15	100566913	100603031	15q26	15q26.3		610350	"LINS1, WINS1, FLJ10583, MRT27"	"Lines, Drosophila, homolog of, 1"	LINS1	55180	ENSG00000140471		"Mental retardation, autosomal recessive 27, 614340 (3), Autosomal recessive"	Lins1 (MGI:1919885)			
chr15	100602549	100651700	15q26.3	15q26.3		615052	ASB7	Ankyrin repeat- and SOCS box-containing protein 7	ASB7	140460	ENSG00000183475			Asb7 (MGI:2152835)			
chr15	100879691	100916625	15q26	15q26.3		600463	"ALDH1A3, ALDH6, MCOP8"	"Aldehyde dehydrogenase 1 family, member A3"	ALDH1A3	220	ENSG00000184254		"Microphthalmia, isolated 8, 615113 (3), Autosomal recessive"	Aldh1a3 (MGI:1861722)			
chr15	100919016	101072889	15q26.3	15q26.3		610986	LRRK1	Leucine-rich repeat kinase 1	LRRK1	79705	ENSG00000154237			Lrrk1 (MGI:2142227)			
chr15	101175722	101251931	15q26.3	15q26.3		608183	"CHSY1, KIAA0990, TPBS"	Carbohydrate synthase 1	CHSY1	22856	ENSG00000131873		"Temtamy preaxial brachydactyly syndrome, 605282 (3), Autosomal recessive"	Chsy1 (MGI:2681120)			
chr15	101270908	101277519	15q26.3	15q26.3		607918	"SELENOS, SEPS1, SELS, VIMP, ADO15"	Selenoprotein S	SELENOS	55829	ENSG00000131871			Selenos (MGI:95994)			
chr15	101281509	101295281	15q26.3	15q26.3		603521	SNRPA1	Small nuclear ribonucleoprotein polypeptide A'	SNRPA1	6627	ENSG00000131876			Snrpa1 (MGI:1916231)			
chr15	101303927	101489983	15q26	15q26.3		167405	"PCSK6, PACE4, SPC4"	Proprotein convertase subtilisin/kexin type 6	PCSK6	5046	ENSG00000140479			Pcsk6 (MGI:102897)			
chr15	101632976	101652390	15q26.3	15q26.3		610014	"TM2D3, BLP2"	TM2 domain-containing protein 3	TM2D3	80213	ENSG00000184277			Tm2d3 (MGI:1915884)			
chr15	0	101991189	Chr.15			120340	COL1AR	"Collagen I, alpha, receptor"	COL1AR	1279							
chr16	0	16700000	16p13			608903	ADHD1	"Attention deficit-hyperactivity disorder, susceptibility to, 1"		450087		max lod at D16S3114	"{Attention deficit-hyperactivity disorder}, 143465 (2), Autosomal dominant"				
chr16	0	16700000	16p13			608558	BMIQ5	Body mass index quantitative trait locus 5	BMIQ5	449016		near D16S404 and D16S764	"[Body mass index QTL5], 608558 (2)"				
chr16	0	16700000	16pter-p13			607339	CHDS1	"Coronary heart disease, susceptibility to, 1"		338334			"{Coronary heart disease, susceptibility to}, 607339 (2)"				
chr16	0	7800000	16p13.3			610543	"DEL16p13.3, RSTSS"	Chromosome 16p13.3 deletion syndrome (Rubinstein-Taybi deletion syndrome)				contiguous gene deletion syndrome	"Chromosome 16p13.3 deletion syndrome, 610543 (4)"				
chr16	0	7800000	16p13.3			613458	"DUP16p13.3, C16DUPq13.3"	Chromosome 16p13.3 duplication syndrome				contiguous gene duplication syndrome	"Chromosome 16p13.3 duplication syndrome, 613458 (4), Autosomal dominant, Isolated cases"				
chr16	0	7800000	16pter-p13.3			141750	"HBHR, ATR1"	"Alpha-thalassemia/mental retardation syndrome, type 1"				contiguous gene syndrome involving deletion of HBA1 and HBA2	"Alpha-thalassemia/mental retardation syndrome, type 1, 141750 (4), Autosomal dominant"				
chr16	0	36800000	16p			606668	IBD8	Inflammatory bowel disease 8	IBD8	170595			"{Inflammatory bowel disease 8}, 606668 (2)"				
chr16	0	28500000	16p13-p12			610260	IHPS2	"Pyloric stenosis, infantile hypertrophic, 2"		780923			"Pyloric stenosis, infantile hypertrophic, 2, 610260 (2)"				
chr16	0	7800000	16p13.3			156850	MCOPCT1	Microphthalmia with cataract 1		8130		proximal to HBA1	"Microphthalmia with cataract 1, 156850 (2), Autosomal dominant"				
chr16	0	7800000	16p13.3			600273	PKDTS	"Polycystic kidney disease, infantile severe, with tuberous sclerosis"				contiguous gene syndrome caused by deletion of TSC2 and PKD1	"Polycystic kidney disease, infantile severe, with tuberous sclerosis, 600273 (4), Autosomal dominant"				
chr16	46978	53631	16p13.3	16p13.3		606007	"POLR3K, RPC11"	"Polymerase III, RNA, subunit K"	POLR3K	51728	ENSG00000161980			Polr3k (MGI:1914255)			
chr16	58058	76354	16p13.3	16p13.3		614403	"RHBDF1, IRHOM1, DIST1"	"Rhomboid 5, Drosophila, homolog of, 1"	RHBDF1	64285	ENSG00000007384			Rhbdf1 (MGI:104328)			
chr16	77018	85850	16pter-p13.3	16p13.3		156565	"MPG, MDG"	N-methylpurine DNA glycosylase	MPG	4350	ENSG00000103152	75kb upstream of HBZ		Mpg (MGI:97073)			
chr16	85800	138697	16p13.3	16p13.3		600928	"NPRL3, CGTHBA, FFEVF3"	Nitrogen permease regulator-like 3	NPRL3	8131	ENSG00000103148		"Epilepsy, familial focal, with variable foci 3, 617118 (3), Autosomal dominant"	Nprl3 (MGI:109258)			
chr16	142421	154510	16pter-p13.3	16p13.3		142310	HBZ	"Hemoglobin, zeta"	HBZ	3050	ENSG00000130656			Hba-x (MGI:96019)			
chr16	165973	166767	16p13.3	16p13.3		609639	HBM	Hemoglobin mu	HBM	3042	ENSG00000206177	?functional					
chr16	172846	173709	16pter-p13.3	16p13.3		141850	"HBA2, HBH"	Hemoglobin alpha-2	HBA2	3040	ENSG00000188536		"Erythrocytosis (3); Heinz body anemia, 140700 (3), Autosomal dominant; Hemoglobin H disease, nondeletional, 613978 (3); Hypochromic microcytic anemia (3); Thalassemia, alpha-, 604131 (3)"	"Hba-a1,Hba-a2 (MGI:96016,MGI:96015)"			
chr16	176650	177521	16pter-p13.3	16p13.3		141800	"HBA1, HBH"	Hemoglobin alpha-1	HBA1	3039	ENSG00000206172	"1, 2, or 3 loci; 5'-zeta-pseudozeta-pseudoalpha-alpha-2-alpha-1-3'"	"Erythremias, alpha- (3); Heinz body anemias, alpha-, 140700 (3), Autosomal dominant; Hemoglobin H disease, nondeletional, 613978 (3); Methemoglobinemias, alpha- (3); Thalassemias, alpha-, 604131 (3)"	"Hba-a1,Hba-a2 (MGI:96016,MGI:96015)"			
chr16	180333	181178	16pter-p13.3	16p13.3		142240	HBQ1	Hemoglobin theta-1	HBQ1	3049	ENSG00000086506			Hbq1b (MGI:3613460)			
chr16	188968	229481	16p13.3	16p13.3		607782	LUC7L	"Luc7, S. cerevisiae, homolog of"	LUC7L	55692	ENSG00000007392			Luc7l (MGI:1914228)			
chr16	268300	275942	16p13.3	16p13.3		603895	RS11	Regulator of G protein signaling 11	RGS11	8786	ENSG00000076344			Rgs11 (MGI:1354739)			
chr16	283136	287214	16p13.3	16p13.3		608012	"PDIA2, PDIP"	"Protein disulfide isomerase, family A, member 2"	PDIA2	64714	ENSG00000185615			Pdia2 (MGI:1916441)			
chr16	287439	355225	16p13.3	16p13.3		603816	"AXIN1, AXIN"	Axis inhibitor 1	AXIN1	8312	ENSG00000103126	hypermethylation of AXIN1 promoter seen in 1 CDUP patient	"?Caudal duplication anomaly, 607864 (3); Hepatocellular carcinoma, somatic, 114550 (3)"	Axin1 (MGI:1096327)			
chr16	367383	370568	16p13.3	16p13.3		604853	"MRPL28, MAAT1"	Mitochondrial ribosomal protein L28	MRPL28	10573	ENSG00000086504			Mrpl28 (MGI:1915861)			
chr16	396754	400753	16p13.3	16p13.3		601818	NME4	"Non-metastatic cells 4, protein expressed in"	NME4	4833	ENSG00000103202			Nme4 (MGI:1931148)			
chr16	401857	412486	16p13.3	16p13.3		615839	"DECR2, PDCR"	"2,4-dienoyl-CoA reductase 2, peroxisomal"	DECR2	26063	ENSG00000242612			Decr2 (MGI:1347059)			
chr16	425620	522484	16p13.3	16p13.3		608738	"RAB11FIP3, EFERIN, KIAA0665"	RAB11 family-interacting protein 3	RAB11FIP3	9727	ENSG00000090565			Rab11fip3 (MGI:2444431)			
chr16	527793	554635	16p13.3	16p13.3		603267	SOLH	"Small optic lobes, Drosophila, homolog of"	CAPN15	6650	ENSG00000103326	conflicting localization to Xq24		Capn15 (MGI:1355075)			
chr16	569967	584135	16p13.3	16p13.3		605754	PIGQ	Phosphatidylinositol glycan anchor biosynthesis class Q protein	PIGQ	9091	ENSG00000007541			Pigq (MGI:1333114)			
chr16	631011	634115	16p13.3	16p13.3		608021	"WFIKKN1, WFIKKN"	"WAP, follistatin, immunoglobulin, Kunitz, and NTR domains-containing protein 1"	WFIKKN1	117166	ENSG00000127578			Wfikkn1 (MGI:2670967)			
chr16	668082	674173	16p13.3	16p13.3		613889	"RHOT2, MIRO2, ARHT2"	"Ras homolog gene family, member T2"	RHOT2	89941	ENSG00000140983			Rhot2 (MGI:2384892)			
chr16	675665	678270	16p13.3	16p13.3		603264	"RHBDL, RRP"	"Rhomboid, Drosophila, homolog of"	RHBDL1	9028	ENSG00000103269			Rhbdl1 (MGI:2384891)			
chr16	680110	682767	16p13.3	16p13.3		607207	"STUB1, CHIP, SCAR16"	STIP1 homologous and U box-containing protein 1	STUB1	10273	ENSG00000103266		"Spinocerebellar ataxia, autosomal recessive 16, 615768 (3), Autosomal recessive"	Stub1 (MGI:1891731)			
chr16	692499	707852	16p13.3	16p13.3		609082	"FBXL16, FBL16, C16orf22"	F-box and leucine-rich repeat protein 16	FBXL16	146330	ENSG00000127585			Fbxl16 (MGI:2448488)			
chr16	715172	719654	16p13.3	16p13.3		610998	METRN	Meteorin	METRN	79006	ENSG00000103260			Metrn (MGI:1917333)			
chr16	722577	726879	16p13.3	16p13.3		614666	"CCDC78, C16orf25, CNM4"	Coiled-coil domain-containing protein 78	CCDC78	124093	ENSG00000162004	mutation identified in 1 CNM4 family	"?Centronuclear myopathy 4, 614807 (3), Autosomal dominant"	Ccdc78 (MGI:2685784)			
chr16	729752	741037	16p13.3	16p13.3		611118	"NARFL, IOP1"	Nuclear prelamin A recognition factor-like	NARFL	64428	ENSG00000103245			Narfl (MGI:1914813)			
chr16	760764	768864	16p13.3	16p13.3		601051	MSLN	Mesothelin	MSLN	10232	ENSG00000102854			Msln (MGI:1888992)			
chr16	788621	798073	16p13.3	16p13.3		613201	"CHTF18, CHL12, CTF18"	"Chromosome transmission fidelity factor 18, S. cerevisiae, homolog of"	CHTF18	63922	ENSG00000127586			Chtf18 (MGI:2384887)			
chr16	798040	800732	16p13.3	16p13.3		607298	GNG13	"Guanine nucleotide-binding protein, gamma-13"	GNG13	51764	ENSG00000127588			Gng13 (MGI:1925616)			
chr16	853631	981612	16p13.3	16p13.3		611761	"LMF1, TMEM112"	Lipase maturation factor 1	LMF1	64788	ENSG00000103227		"Lipase deficiency, combined, 246650 (3), Autosomal recessive"	Lmf1 (MGI:1923733)			
chr16	981807	986978	16p13.3	16p13.3		605923	SOX8	SRY-box 8	SOX8	30812	ENSG00000005513			Sox8 (MGI:98370)			
chr16	1072755	1081453	16p13.3	16p13.3		182455	SSTR5	Somatostatin receptor-5	SSTR5	6755	ENSG00000162009		"Somatostatin analog, resistance to (3)"	Sstr5 (MGI:894282)			
chr16	1088225	1096305	16p13.3	16p13.3		614147	"C1QTNF8, CTRP8"	C1q- and tumor necrosis factor-related protein 8	C1QTNF8	390664	ENSG00000184471						
chr16	1153240	1221771	16p13.3	16p13.3		607904	"CACNA1H, EIG6, ECA6, HALD4"	"Calcium channel, voltage-dependent, T type, alpha-1H subunit"	CACNA1H	8912	ENSG00000196557		"{Epilepsy, childhood absence, susceptibility to, 6}, 611942 (3); {Epilepsy, idiopathic generalized, susceptibility to, 6}, 611942 (3); Hyperaldosteronism, familial, type IV, 617027 (3), Autosomal dominant"	Cacna1h (MGI:1928842)			
chr16	1221650	1226453	16p13.3	16p13.3		609341	"TPSG1, TMT"	"Tryptase, gamma-1"	TPSG1	25823	ENSG00000116176			Tpsg1 (MGI:1349391)			
chr16	1228335	1230183	16p13.3	16p13.3		191081	"TPSB2, TPS2"	"Tryptase, beta 2"	TPSB2	64499	ENSG00000197253			Tpsb2 (MGI:96942)			
chr16	1240676	1242553	16p13.3	16p13.3		191080	"TPSAB1, TPS1"	"Tryptase, alpha/beta-1"	TPSAB1	7177	ENSG00000172236			Tpsb2 (MGI:96942)			
chr16	1256271	1258492	16p13.3	16p13.3		609272	"TPSD1, MCP7L1"	"Tryptase, delta-1"	TPSD1	23430	ENSG00000095917						
chr16	1309152	1327017	16p13.3	16p13.3		601661	UBE2I	Ubiquitin-conjugating enzyme E2I (homologous to yeast UBC9)	UBE2I	7329	ENSG00000103275			Ube2i (MGI:107365)			
chr16	1333604	1349440	16p13.3	16p13.3		604009	"BAIAP3, BAP3"	BAI1-associated protein 3	BAIAP3	8938	ENSG00000007516			Baiap3 (MGI:2685783)			
chr16	1349239	1351871	16p13.3	16p13.3		617058	TSR3	"TSR3, aminocarboxypropyl transferase ribosome maturation factor"	TSR3	115939	ENSG00000007520			Tsr3 (MGI:1915577)			
chr16	1351898	1363350	16p	16p13.3		607838	GNPTAG	"N-acetylglucosamine-1-phosphotransferase, gamma subunit"	GNPTG	84572	ENSG00000090581		"Mucolipidosis III gamma, 252605 (3), Autosomal recessive"	Gnptg (MGI:2147006)			
chr16	1363204	1414748	16p13.3	16p13.3		617463	"UNKL, ZC3H5L, C16orf28"	Unkempt family-like zinc finger	UNKL	64718	ENSG00000059145			Unkl (MGI:1921404)			
chr16	1444932	1475083	16p13	16p13.3		602727	"CLCN7, CLC7, OPTA2, OPTB4"	Chloride channel-7	CLCN7	1186	ENSG00000103249		"Osteopetrosis, autosomal dominant 2, 166600 (3), Autosomal dominant; Osteopetrosis, autosomal recessive 4, 611490 (3)"	Clcn7 (MGI:1347048)			
chr16	1485938	1488908	16p13.3	16p13.3		613442	PTX4	"Pentraxin 4, long"	PTX4	390667	ENSG00000251692			Ptx4 (MGI:1915759)			
chr16	1493344	1510458	16p13.3	16p13.3		611140	"TELO2, TEL2, CLK2, KIAA0683, HCLK2, YHFS"	"Telomere maintenance 2, S. cerevisiae, homolog of"	TELO2	9894	ENSG00000100726		"You-Hoover-Fong syndrome, 616954 (3), Autosomal recessive"	Telo2 (MGI:1918968)			
chr16	1510426	1612107	16p13.3	16p13.3		614620	"IFT140, KIAA0590, SRTD9, MZSDS, RP80"	"Intraflagellar transport 140, Chlamydomonas, homolog of"	IFT140	9742	ENSG00000187535		"Retinitis pigmentosa 80, 617781 (3), Autosomal recessive; Short-rib thoracic dysplasia 9 with or without polydactyly, 266920 (3), Autosomal recessive"	Ift140 (MGI:2146906)			
chr16	1528740	1555579	16p13.3	16p13.3		611002	"TMEM204, C16orf30, CLP24"	Transmembrane protein 204	TMEM204	79652	ENSG00000131634			Tmem204 (MGI:3039635)			
chr16	1706182	1770316	16p13.3	16p13.3		605431	"MAPK8IP3, SYD2, JSAP1, JIP3"	Mitogen-activated protein kinase 8-interacting protein 3	MAPK8IP3	23162	ENSG00000138834			Mapk8ip3 (MGI:1353598)			
chr16	1770319	1771749	16q13	16p13.3		601817	"NME3, NM23H3"	"Nonmetastatic cells 3, protein expressed in"	NME3	4832	ENSG00000103024			Nme3 (MGI:1930182)			
chr16	1771888	1773150	16q13-q21	16p13.3		611994	"MRPS34, MRPS12, COXPD32"	Mitochondrial ribosomal protein S34	MRPS34	65993	ENSG00000074071		"Combined oxidative phosphorylation deficiency 32, 617664 (3), Autosomal recessive"	Mrps34 (MGI:1930188)			
chr16	1773221	1776713	16p13.3	16p13.3		610886	EME2	"Essential meiotic endonuclease 1, S. pombe, homolog of, 2"	EME2	197342	ENSG00000197774			Eme2 (MGI:1919889)			
chr16	1776711	1782579	16p13.3	16p13.3		611659	"SPSB3, SSB3"	SPRY domain- and SOCS box-containing 3	SPSB3	90864	ENSG00000162032			Spsb3 (MGI:1891471)			
chr16	1782922	1789190	16p13.3	16p13.3		610779	"NUBP2, CFD1"	Nucleotide-binding protein 2	NUBP2	10101	ENSG00000095906			Nubp2 (MGI:1347072)			
chr16	1790412	1794907	16p13.3	16p13.3		601489	"IGFALS, ALS, ACLSD"	"Insulin-like growth factor-binding protein, acid-labile subunit"	IGFALS	3483	ENSG00000099769		"Acid-labile subunit, deficiency of, 615961 (3)"	Igfals (MGI:107973)			
chr16	1809102	1827193	16p13	16p13.3		138760	"HAGH, GLO2"	Hydroxyacyl glutathione hydrolase; glyoxalase II	HAGH	3029	ENSG00000063854		"[Glyoxalase II deficiency], 614033 (1), Autosomal dominant"	Hagh (MGI:95745)			
chr16	1827223	1840206	16p13.3	16p13.3		616320	"FAHD1, FLJ36880"	Fumarylacetoacetate hydrolase domain-containing protein 1	FAHD1	81889	ENSG00000180185			Fahd1 (MGI:1915886)			
chr16	1833982	1872177	16p13.3	16p13.3		617670	"MEIOB, SPGF22"	Meiosis-specific protein with OB domains	MEIOB	254528	ENSG00000162039	mutation identified in one SPGF22 family	"?Spermatogenic failure 22, 617706 (3), Autosomal recessive"	Meiob (MGI:1922428)			
chr16	1938228	1943325	16p13.3	16p13.3		606216	"MSRB1, SEPX1, SELX"	Methionine sulfoxide reductase B1	MSRB1	51734	ENSG00000198736			Msrb1 (MGI:1351642)			
chr16	1944570	1955122	16p13.3	16p13.3		617416	RPL3L	Ribosomal protein L3-like	RPL3L	6123	ENSG00000140986			Rpl3l (MGI:1913461)			
chr16	1959515	1961974	16p13.3	16p13.3		603843	NDUFB10	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 10"	NDUFB10	4716	ENSG00000140990			Ndufb10 (MGI:1915592)			
chr16	1962060	1964825	16p13.3	16p13.3		603624	RPS2	Ribosomal protein S2	RPS2	6187	ENSG00000140988			Rps2 (MGI:105110)			
chr16	1972062	1978749	16p13.3	16p13.3		605915	TBL3	Transducin-beta-like 3	TBL3	10607	ENSG00000183751			Tbl3 (MGI:2384863)			
chr16	1978916	1984026	16p13	16p13.3		611256	NOXO1	NADPH oxidase organizer 1	NOXO1	124056	ENSG00000196408			Noxo1 (MGI:1919143)			
chr16	1984148	1987748	16p13.3-p13.12	16p13.3		600924	"GFER, ERV1, ALR"	"Growth factor, erv1, S. cerevisiae, homolog of (augmenter of liver regeneration)"	GFER	2671	ENSG00000127554		"Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay, 613076 (3)"	Gfer (MGI:107757)			
chr16	1989944	1994274	16pter	16p13.3		603927	SYNGR3	Synaptogyrin 3	SYNGR3	9143	ENSG00000127561			Syngr3 (MGI:1341881)			
chr16	1997651	2009820	16p13.3	16p13.3		617508	ZNF598	Zinc finger protein 598	ZNF598	90850	ENSG00000167962			Zfp598 (MGI:2670965)			
chr16	2019519	2020754	16p13.3	16p13.3		607997	"NPW, PPNPW, PPL8"	Neuropeptide W	NPW	283869	ENSG00000183971			Npw (MGI:2685781)			
chr16	2026867	2039025	16p13.3	16p13.3		606553	"SLC9A3R2, SIP1, NHERF2"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulatory factor 2"	SLC9A3R2	9351	ENSG00000065054			Slc9a3r2 (MGI:1890662)			
chr16	2039814	2047871	16p13.3-p13.2	16p13.3		602656	"NTHL1, OCTS3, FAP3"	"Endonuclease III, E. coli, homolog of"	NTHL1	4913	ENSG00000065057		"Familial adenomatous polyposis 3, 616415 (3), Autosomal recessive"	Nthl1 (MGI:1313275)			
chr16	2047803	2088719	16p13.3	16p13.3		191092	"TSC2, LAM"	Tuberin (tuberous sclerosis 2 gene)	TSC2	7249	ENSG00000103197	somatic mutation identified in 1 FCORD2 patient	"?Focal cortical dysplasia, type II, somatic, 607341 (3); Lymphangioleiomyomatosis, somatic, 606690 (3); Tuberous sclerosis-2, 613254 (3), Autosomal dominant"	Tsc2 (MGI:102548)			
chr16	2088707	2135897	16p13.3-p13.12	16p13.3		601313	PKD1	Polycystin-1	PKD1	5310	ENSG00000008710		"Polycystic kidney disease 1, 173900 (3), Autosomal dominant"	Pkd1 (MGI:97603)			
chr16	2090194	2090283	16p13.3	16p13.3		611621	"MIR1225, MIRN1225"	Micro RNA 1225	MIR1225	100188847							
chr16	2148143	2154164	16p13.3	16p13.3		605455	RAB26	RAS-associated protein RAB26	RAB26	25837	ENSG00000167964			Rab26 (MGI:2443284)			
chr16	2155777	2178128	16p13.3	16p13.3		606692	"TRAF7, RFWD1"	TNF receptor-associated factor 7	TRAF7	84231	ENSG00000131653			Traf7 (MGI:3042141)			
chr16	2177182	2196505	16p13.3	16p13.3		612184	"CASKIN1, KIAA1306"	CASK-interacting protein 1	CASKIN1	57524	ENSG00000167971			Caskin1 (MGI:2442952)			
chr16	2204627	2209453	16p13.3	16p13.3		612190	"MLST8, GBL, LST8, WAT1, POP3"	MTOR-associated protein LST8	MLST8	64223	ENSG00000167965			Mlst8 (MGI:1929514)			
chr16	2211601	2214820	16p13.3	16p13.3		172280	PGP	Phosphoglycolate phosphatase	PGP	283871	ENSG00000184207	no recombination with PKD1		Pgp (MGI:1914328)			
chr16	2223487	2235741	16p13.3	16p13.3		603022	"E4F1, E4F"	E4F transcription factor 1	E4F1	1877	ENSG00000167967			E4f1 (MGI:109530)			
chr16	2239871	2251600	16p13.3	16p13.3		600305	"ECI1, DCI"	Enoyl-CoA delta isomerase 1	ECI1	1632	ENSG00000167969			Eci1 (MGI:94871)			
chr16	2275877	2340745	16p13.3	16p13.3		601615	"ABCA3, ABC3, SMDP3"	ATP-binding cassette-3	ABCA3	21	ENSG00000167972		"Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3), Autosomal recessive"	Abca3 (MGI:1351617)			
chr16	2429390	2458857	16p13.3	16p13.3		600227	"CCNF, FBX1"	Cyclin F	CCNF	899	ENSG00000162063			Ccnf (MGI:102551)			
chr16	2471498	2474144	16p13.3	16p13.3		602349	NTN2L	"Netrin-2, chicken, homolog of, like"	NTN3	4917	ENSG00000162068			Ntn3 (MGI:1341188)			
chr16	2475103	2509668	16p13.3	16p13.3		613577	"TBC1D24, KIAA1171, FIME, EIEE16, DOORS, DFNB86, DFNA65"	"TBC1 domain family, member 24"	TBC1D24	57465	ENSG00000162065		"DOORS syndrome, 220500 (3), Autosomal recessive; Deafness , autosomal recessive 86, 614617 (3), Autosomal recessive; Deafness, autosomal dominant 65, 616044 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 16, 615338 (3), Autosomal recessive; Myoclonic epilepsy, infantile, familial, 605021 (3), Autosomal recessive"	Tbc1d24 (MGI:2443456)			
chr16	2513725	2520222	16p13.3	16p13.3		108745	"ATP6V0C, ATP6L, ATP6C"	"ATPase, H+ transporting, lysosomal, 16kD, V0 subunit c"	ATP6V0C	527	ENSG00000185883			Atp6v0c (MGI:88116)			
chr16	2530034	2531407	16p13.3	16p13.3		611113	"CEMP1, CP23"	Cementum protein 1	CEMP1	752014	ENSG00000205923						
chr16	2537963	2603189	16p13.3	16p13.3		605213	"PDPK1, PDK1"	3-phosphoinositide-dependent protein kinase 1	PDPK1	5170	ENSG00000140992			Pdpk1 (MGI:1338068)			
chr16	2682493	2709029	16p13.3	16p13.3		611285	KCTD5	Potassium channel tetramerization domain-containing protein 5	KCTD5	54442	ENSG00000167977			Kctd5 (MGI:1916509)			
chr16	2750902	2771411	Chr.16	16p13.3		606032	"SRRM2, SRM300, KIAA0324"	"Serine/arginine repetitive matrix 2 (ser/arg-rich splicing factor-related nuclear matrix protein, 300kD)"	SRRM2	23524	ENSG00000167978						
chr16	2771413	2777295	16p13.3	16p13.3		600787	"TCEB2, ELOB"	"Transcription elongation factor B, polypeptide 2"	ELOB	6923	ENSG00000103363						
chr16	2783952	2787758	16p13.3	16p13.3		613797	"PRSS33, EOS"	"Protease, serine, 33"	PRSS33	260429	ENSG00000103355			Prss33 (MGI:2661234)			
chr16	2817162	2821721	16p13.3	16p13.3		608159	"PRSS21, ESP1"	"Protease, serine, 21 (testisin)"	PRSS21	10942	ENSG00000007038			Prss21 (MGI:1916698)			
chr16	2852726	2858629	16p13.3	16p13.3		609343	PRSS22	"Protease, serine, 22"	PRSS22	64063	ENSG00000005001			Prss22 (MGI:1918085)			
chr16	2964215	2968382	16p13.3	16p13.3		609899	"KREMEN2, KRM2"	Kringle domain-containing transmembrane protein 2	KREMEN2	79412	ENSG00000131650			Kremen2 (MGI:1920266)			
chr16	2969244	2973488	16p13.3	16p13.3		614578	PAQR4	"Progestin and ADIPOQ receptor family, member 4"	PAQR4	124222	ENSG00000162073			Paqr4 (MGI:1923748)			
chr16	2972790	2980538	16p13.3	16p13.3		602474	"PKMYT1, MYT1"	"Protein kinase, membrane-associated tyrosine/threonine, 1"	PKMYT1	9088	ENSG00000127564			Pkmyt1 (MGI:2137630)			
chr16	3012455	3014504	16p13.3	16p13.3		615799	CLDN9	Claudin 9	CLDN9	9080	ENSG00000213937			Cldn9 (MGI:1913100)			
chr16	3014711	3018186	16p13.3	16p13.3		615798	CLDN6	Claudin 6	CLDN6	9074	ENSG00000184697			Cldn6 (MGI:1859284)			
chr16	3020311	3022382	16p13.3	16p13.3		605914	"TNFRSF12A, FN14, TWEAKR"	"Tumor necrosis factor receptor superfamily, member 12A"	TNFRSF12A	51330	ENSG00000006327			Tnfrsf12a (MGI:1351484)			
chr16	3024018	3027754	16p13.3	16p13.3		615403	"THOC6, FSAP35, BBIS"	THO complex subunit 6	THOC6	79228	ENSG00000131652		"Beaulieu-Boycott-Innes syndrome, 613680 (3), Autosomal recessive"	Thoc6 (MGI:2677480)			
chr16	3027709	3036984	16p13.3	16p13.3		617003	"BICDL2, BICDR2, CCDC64B"	BICD family-like cargo adaptor 2	BICDL2	146439	ENSG00000162069			Bicdl2 (MGI:2388267)			
chr16	3045962	3060728	16p13.3	16p13.3		608482	"MMP25, MMP20A"	Matrix metalloproteinase 25	MMP25	64386	ENSG00000008516			Mmp25 (MGI:2443938)			
chr16	3065311	3069818	16p13.3	16p13.3		606001	"IL32, NK4"	Interleukin 32	IL32	9235	ENSG00000008517						
chr16	3112561	3120516	16p13.3	16p13.3		603436	"ZNF205, ZNF210"	Zinc finger protein-205	ZNF205	7755	ENSG00000122386			Zfp13 (MGI:99159)			
chr16	3135055	3142803	16p13.3	16p13.3		608387	"ZNF213, CR53"	Zinc finger protein 213	ZNF213	7760	ENSG00000085644			Zfp213 (MGI:3053094)			
chr16	3188203	3206558	16p13	16p13.3		603232	"OR1F1, OLFMF"	"Olfactory receptor, family 1, subfamily F, member 1"	OR1F1	4992	ENSG00000168124						
chr16	3222324	3236220	16p13	16p13.3		603231	ZNF200	Zinc finger protein-200	ZNF200	7752	ENSG00000010539						
chr16	3242027	3256775	16p13	16p13.3		608107	"MEFV, MEF, FMF"	Pyrin (marenostrin)	MEFV	4210	ENSG00000103313	between D16S80 and D16S283	"Familial Mediterranean fever, AD, 134610 (3), Autosomal dominant; Familial Mediterranean fever, AR, 249100 (3), Autosomal recessive"	Mefv (MGI:1859396)			
chr16	3283182	3301648	16p13.3	16p13.3		604191	ZNF263	Zinc finger protein 263	ZNF263	10127	ENSG00000006194			Zfp263 (MGI:1921370)			
chr16	3298807	3305438	16p13	16p13.3		612969	"TIGD7, SANCHO"	Tigger transposable element-derived gene 7	TIGD7	91151	ENSG00000140993						
chr16	3305405	3322998	16pter-p11	16p13.3		601473	ZNF75A	Zinc finger protein-75A	ZNF75A	7627	ENSG00000162086						
chr16	3401189	3409363	16p13.3	16p13.3		603900	ZNF174	Zinc finger protein-174	ZNF174	7727	ENSG00000103343			Zfp174 (MGI:2686600)			
chr16	3432421	3443536	16p13.3	16p13.3		614685	ZNF597	Zinc finger protein 597	ZNF597	146434	ENSG00000167981			Zfp597 (MGI:1918313)			
chr16	3443610	3486962	16p13.3	16p13.3		614246	"NAA60, NAT15"	"N-alpha-acetyltransferase 60, NatF catalytic subunit"	NAA60	79903	ENSG00000122390			Naa60 (MGI:1922013)			
chr16	3500930	3539047	16p13	16p13.3		616787	"CLUAP1, QILIN, FAP22, KIAA0643"	Clusterin-associated protein 1	CLUAP1	23059	ENSG00000103351			Cluap1 (MGI:1924029)			
chr16	3539032	3577781	16p13.3	16p13.3		615648	NLRC3	"NLR family, Caspase recruitment domain-containing 3"	NLRC3	197358	ENSG00000167984			Nlrc3 (MGI:2444070)			
chr16	3579652	3611638	16p13.3	16p13.3		613278	"SLX4, BTBD12, MUS312, KIAA1784, KIAA1987, FANCP"	"Slx4, S. cerevisiae, homolog of"	SLX4	84464	ENSG00000188827		"Fanconi anemia, complementation group P, 613951 (3), Autosomal recessive"	Slx4 (MGI:106299)			
chr16	3611736	3665471	16p13.3	16p13.3		125505	"DNASE1, DNL1"	Deoxyribonuclease I	DNASE1	1773	ENSG00000213918		"{Systemic lupus erythematosus, susceptibility to}, 152700 (3), Autosomal dominant"	Dnase1 (MGI:103157)			
chr16	3658036	3717596	16p13.3	16p13.3		606219	"TRAP1, HSP75, HSP90L"	Tumor necrosis factor receptor-associated protein 1	TRAP1	10131	ENSG00000126602			Trap1 (MGI:1915265)			
chr16	3725053	3880726	16p13.3	16p13.3		600140	"CREBBP, CBP, RSTS1"	CREB binding protein	CREBBP	1387	ENSG00000005339	fusion partner with MORF in AML; fusion partner with MLL in therapy-related acute leukemia; fusion partner with MOZ in AML	"Rubinstein-Taybi syndrome 1, 180849 (3), Autosomal dominant"	Crebbp (MGI:1098280)			
chr16	3953386	4116184	16p13.3	16p13.3		603302	ADCY9	Adenylate cyclase-9	ADCY9	115	ENSG00000162104			Adcy9 (MGI:108450)			
chr16	4189373	4242252	16p13.3	16p13.3		604992	SRL	Sarcalumenin	SRL	6345	ENSG00000185739			Srl (MGI:2146620)			
chr16	4257185	4272999	16p13	16p13.3		600743	TFAP4	Transcription factor AP-4 (activating enhancer-binding protein 4)	TFAP4	7023	ENSG00000090447			Tfap4 (MGI:103239)			
chr16	4314760	4339596	16p13.3	16p13.3		608539	"GLIS2, NPHP7"	GLIS family zinc finger protein 2	GLIS2	84662	ENSG00000126603		"Nephronophthisis 7, 611498 (3)"	Glis2 (MGI:1932535)			
chr16	4340248	4351398	16p13.3	16p13.3		614336	"PAM16, MAGMAS, SMDMDM"	"Presequence translocase-associated motor 16, S. cerevisiae, homolog of"	PAM16	51025	ENSG00000217930		"Spondylometaphyseal dysplasia, Megarbane-Dagher-Melike type, 613320 (3), Autosomal recessive"	Pam16 (MGI:1913699)			
chr16	4354541	4416960	16p13.3	16p13.3		611668	"CORO7, POD1, CRN7"	Coronin 7	CORO7	79585	ENSG00000262246			Coro7 (MGI:1926135)			
chr16	4371847	4383527	16p13.3	16p13.3		608843	VASN	Vasorin	VASN	114990	ENSG00000168140			Vasn (MGI:2177651)			
chr16	4425804	4456774	16p13.3	16p13.3		608382	"DNAJA3, TID1"	"DNAJ, E. coli, homolog of, subfamily A, member 3"	DNAJA3	9093	ENSG00000103423			Dnaja3 (MGI:1933786)			
chr16	4474696	4510346	16p13.3	16p13.3		141251	HMOX2	Heme oxygenase 2	HMOX2	3163	ENSG00000103415			Hmox2 (MGI:109373)			
chr16	4510674	4538814	16p13.3	16p13.3		610503	C16orf5	Chromosome 16 open reading frame 5	CDIP1	29965	ENSG00000089486			Cdip1 (MGI:1913876)			
chr16	4616492	4690973	16p13.3	16p13.3		607559	"MGRN1, KIAA0544"	"Mahogunin, ring finger 1"	MGRN1	23295	ENSG00000102858			Mgrn1 (MGI:2447670)			
chr16	4688929	4695858	16p13.3	16p13.3		617338	"NUDT16L1, SDOS"	Nudix hydrolase 16-like 1	NUDT16L1	84309	ENSG00000168101			Nudt16l1 (MGI:1914161)			
chr16	4696509	4734376	16p13.3	16p13.3		617310	ANKS3	Ankyrin repeat and sterile alpha motif domains-containing protein 3	ANKS3	124401	ENSG00000168096			Anks3 (MGI:1919865)			
chr16	4777589	4791609	16p13.3	16p13.3		611562	"SEPT12, SPGF10"	Septin 12	12-Sep	124404	ENSG00000140623		"Spermatogenic failure 10, 614822 (3), Autosomal dominant"	Sept12 (MGI:1918339)			
chr16	4796961	4802949	16p13.3	16p13.3		614574	"ROGDI, KTZS"	"Rogdi, Drosophila, homolog of"	ROGDI	79641	ENSG00000067836		"Kohlschutter-Tonz syndrome, 226750 (3), Autosomal recessive"	Rogdi (MGI:1913299)			
chr16	4803202	4848031	16p13.3	16p13.3		610660	"GLYR1, NP60"	Glyoxylate reductase 1 homolog	GLYR1	84656	ENSG00000140632			Glyr1 (MGI:1921272)			
chr16	4846664	4882400	16p13.3	16p13.3		609771	UBN1	Ubinuclein 1	UBN1	29855	ENSG00000118900			Ubn1 (MGI:1891307)			
chr16	4882506	4937134	16p13	16p13.3		602871	PPL	Periplakin	PPL	5493	ENSG00000118898			Ppl (MGI:1194898)			
chr16	5024843	5033940	16p13.3	16p13.3		607985	"NAGPA, UCE"	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA	51172	ENSG00000103174			Nagpa (MGI:1351598)			
chr16	5071808	5087378	16p13.3	16p13.3		605907	"ALG1, HMAT1, HMT1, CDG1K"	"Alg1, yeast, homolog of (beta-1,4 mannosyltransferase)"	ALG1	56052	ENSG00000033011		"Congenital disorder of glycosylation, type Ik, 608540 (3), Autosomal recessive"	Alg1 (MGI:2384774)			
chr16	5084297	5097819	16p13.3	16p13.3		615263	"EEF2KMT, FAM86A"	Eukaryotic elongation factor 2 lysine methyltransferase	EEF2KMT	196483	ENSG00000118894			Eef2kmt (MGI:1917761)			
chr16	5239751	7713342	16p13	16p13.3		605104	"RBFOX1, 2BP1, FOX1, HRNBP1"	"RNA-binding protein FOX1, C. elegans, homolog of, 1"	RBFOX1	54715	ENSG00000078328			Rbfox1 (MGI:1926224)			
chr16	7800000	10400000	16p13.2			616863	"DEL16p13.2, C16DELp13.2"	Chromosome 16p13.2 deletion syndrome					"Chromosome 16p13.2 deletion syndrome, 616863 (4), Autosomal dominant"				
chr16	8526548	8590192	16p13.3	16p13.2		611579	TMEM114	Transmembrane protein 114	TMEM114	283953	ENSG00000232258			Tmem114 (MGI:1921970)			
chr16	8621639	8673564	16p13.2	16p13.2		615261	"METTL22, C16orf68"	Methyltransferase-like 22	METTL22	79091				Mettl22 (MGI:2384301)			
chr16	8674586	8784574	16p13.3	16p13.2		137150	"ABAT, GABAT"	4-aminobutyrate aminotransferase	ABAT	18	ENSG00000183044		"GABA-transaminase deficiency, 613163 (3), Autosomal recessive"	Abat (MGI:2443582)			
chr16	8797812	8849336	16p13.3-p13.2	16p13.2		601785	"PMM2, CDG1A"	Phosphomannomutase 2	PMM2	5373	ENSG00000140650		"Congenital disorder of glycosylation, type Ia, 212065 (3), Autosomal recessive"	Pmm2 (MGI:1859214)			
chr16	8852941	8869011	16p13.2	16p13.2		616885	"CARHSP1, CRHSP24"	Calcium-regulated heat-stable protein 1	CARHSP1	23589	ENSG00000153048			Carhsp1 (MGI:1196368)			
chr16	8892093	8963911	16p13.3	16p13.2		602519	"USP7, HAUSP"	"Ubiquitin-specific protease-7, herpes virus-associated"	USP7	7874	ENSG00000187555	previously reported to map to 3p21		Usp7 (MGI:2182061)			
chr16	9753403	10182927	16p13	16p13.2		138253	"GRIN2A, NMDAR2A, FESD, LKS"	"Glutamate receptor, ionotropic, N-methyl D-aspartate 2A"	GRIN2A	2903	ENSG00000183454		"Epilepsy, focal, with speech disorder and with or without mental retardation, 245570 (3), Autosomal dominant"	Grin2a (MGI:95820)			
chr16	10385998	10483642	16p13.13	16p13.2-p13.1		613645	"ATF7IP2, MCAF2"	Activating transcription factor 7-interacting protein 2	ATF7IP2	80063	ENSG00000166669			"Gm24392,Atf7ip2 (MGI:5454169,MGI:1922579)"			
chr16	10400000	12500000	16p13.13			617901	"DEXI, MYLE"	Dexamethasone-induced gene									
chr16	10528421	10580715	16p13.2	16p13.13		602334	"EMP2, NPHS10"	Epithelial membrane protein 2	EMP2	2013	ENSG00000213853		"Nephrotic syndrome, type 10, 615861 (3), Autosomal recessive"	Emp2 (MGI:1098726)			
chr16	10743163	10769350	16p13.1	16p13.13		600280	"NUBP1, NBP"	Nucleotide-binding protein 1	NUBP1	4682	ENSG00000103274			Nubp1 (MGI:1347073)			
chr16	10866207	10941561	16p13	16p13.13		600005	"CIITA, MHC2TA, C2TA"	Class II major histocompatibility complex transactivator	CIITA	4261	ENSG00000179583		"Bare lymphocyte syndrome, type II, complementation group A, 209920 (3), Autosomal recessive; {Rheumatoid arthritis, susceptibility to}, 180300 (3)"	Ciita (MGI:108445)			
chr16	10944487	11193271	16p13.13	16p13.13		611303	"CLEC16A, KIAA0350"	"C-type lectin domain family 16, member A"	CLEC16A	23274	ENSG00000038532			Clec16a (MGI:1921624)			
chr16	11254416	11256181	16p13.2	16p13.13		603597	"SOCS1, SSI1, CIS1, CISH1"	Suppressor of cytokine signaling 1	SOCS1	8651	ENSG00000185338			Socs1 (MGI:1354910)			
chr16	11267856	11269302	16p13.3	16p13.13		190232	TNP2	Transition protein-2 (during histone to protamine replacement)	TNP2	7142	ENSG00000178279	in 13kb segment with PRM1 and PRM2					
chr16	11275635	11276479	16p13.3	16p13.13		182890	PRM2	Sperm protamine P2	PRM2	5620	ENSG00000122304	in same 4.8kb fragment as PRM2					
chr16	11280835	11281334	16p13.3	16p13.13		182880	PRM1	Sperm protamine P1	PRM1	5619	ENSG00000175646	16q21 = conflicting localization					
chr16	11345437	11351762	16p13.13	16p13.13		612426	"C16orf75, RMI2, BLAP18"	"BLM-associated protein, 18kD"	RMI2	116028	ENSG00000175643			Rmi2 (MGI:2685383)			
chr16	11547721	11636376	16p13.3-p12	16p13.13		603795	"LITAF, CMT1C"	LPS-induced TNFA factor	LITAF	9516	ENSG00000189067		"Charcot-Marie-Tooth disease, type 1C, 601098 (3), Autosomal dominant"	Litaf (MGI:1929512)			
chr16	11668432	11679158	16p13	16p13.13		603032	SNN	Stannin	SNN	8303	ENSG00000184602			Snn (MGI:1276549)			
chr16	11679079	11742877	16p13.13	16p13.13		617792	"TXNDC11, EFP1"	Thioredoxin domain-containing protein 11	TXNDC11	51061	ENSG00000153066			Txndc11 (MGI:1923620)			
chr16	11819829	11828831	16p13.13	16p13.13		613746	BCAR4	Breast cancer antiestrogen resistance 4	BCAR4	400500							
chr16	11834195	11851584	16p13	16p13.13		615874	"RSL1D1, CSIG, PBK1"	Ribosomal L1 domain-containing protein 1	RSL1D1	26156	ENSG00000171490			Rsl1d1 (MGI:1913659)			
chr16	11868127	11916661	16p13.1	16p13.13		139259	GSPT1	G1 to S phase transition-1	GSPT1	2935	ENSG00000103342			Gspt1 (MGI:1316728)			
chr16	11965106	11968067	16p13.1	16p13.13		109545	"TNFRSF17, BCMA"	"Tumor necrosis factor receptor superfamily, member 17 (B-cell maturation factor)"	TNFRSF17	608	ENSG00000048462			Tnfrsf17 (MGI:1343050)			
chr16	12659798	12803886	16p13.12	16p13.12		615603	CPPED1	Calcineurin-like phosphoesterase domain-containing protein 1	CPPED1	55313	ENSG00000103381			Cpped1 (MGI:2443300)			
chr16	12901618	13563426	16p13.12	16p13.12		613346	"SHISA9, CKAMP44"	"Shisa family, member 9"	SHISA9	729993	ENSG00000237515			Shisa9 (MGI:1919805)			
chr16	13920136	13952347	16p13.3-p13.13	16p13.12		133520	"ERCC4, XPF, FANCQ, XFEPS"	"Excision-repair, complementing defective, in Chinese hamster, number 4"	ERCC4	2072	ENSG00000175595	mutation identified in 1 XFEPS patient	"Fanconi anemia, complementation group Q, 615272 (3), Autosomal recessive; ?XFE progeroid syndrome, 610965 (3); Xeroderma pigmentosum, group F, 278760 (3), Autosomal recessive; Xeroderma pigmentosum, type F/Cockayne syndrome, 278760 (3), Autosomal recessive"	Ercc4 (MGI:1354163)			
chr16	14071071	14266778	16p13.1	16p13.12		609463	"MKL2, MRTFB"	MKL1/myocardin-like 2	MKL2	57496	ENSG00000186260			Mkl2 (MGI:3050795)			
chr16	14303966	14304048	16p13.12	16p13.12		614734	MIR193B	Micro RNA 193B	MIR193B	574455							
chr16	14309284	14309370	16p13.12	16p13.12		614735	MIR365A	Micro RNA 365A	MIR365A	100126355							
chr16	14435699	14630285	16p13.12	16p13.12		604212	"PARN, DAN, DKCB6, PFBMFT4"	Polyadenylate-specific ribonuclease	PARN	5073	ENSG00000140694		"Dyskeratosis congenita, autosomal recessive 6, 616353 (3), Autosomal recessive; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, 616371 (3), Autosomal dominant"	Parn (MGI:1921358)			
chr16	14672547	14694661	16p13.1-p12	16p13.12		603603	"PLA2G10, SPLA2, GXSPLA2"	"Phospholipase A2, group X"	PLA2G10	8399	ENSG00000069764			Pla2g10 (MGI:1347522)			
chr16	14833785	14896156	16p13.11	16p13.11		609157	NOMO1	Nodal modulator 1	NOMO1	23420	ENSG00000103512			Nomo1 (MGI:2385850)			
chr16	14937442	14952059	16p13.1	16p13.11		606406	NPIP	Nuclear pore complex-interacting protein	NPIPA1	9284	ENSG00000183426						
chr16	14974590	15153342	16p13.11	16p13.11		614244	"PDXDC1, KIAA0251"	Pyridoxal-dependent decarboxylase domain-containing protein 1	PDXDC1	23042	ENSG00000179889			Pdxdc1 (MGI:1920909)			
chr16	15037852	15056078	16p13.11	16p13.11		615367	NTAN1	N-terminal asparagine amidase	NTAN1	123803	ENSG00000157045			Ntan1 (MGI:108471)			
chr16	15060021	15094334	16p12	16p13.11		605121	"RRN3, TIFIA"	"RRN3, S. cerevisiae, homolog of"	RRN3	54700	ENSG00000085721			Rrn3 (MGI:1925255)			
chr16	15594368	15643165	16p13.13	16p13.11		614593	"MARF1, KIAA0430, LKAP"	Meiosis regulator and mRNA stability factor 1	MARF1	9665	ENSG00000166783			Marf1 (MGI:2444505)			
chr16	15643266	15726352	16p13.1	16p13.11		609449	"NDE1, NUDE, LIS4, MHAC"	nudE neurodevelopment protein 1	NDE1	54820	ENSG00000072864	mutation identified in 1 MHAC family	"Lissencephaly 4 (with microcephaly), 614019 (3), Autosomal recessive; ?Microhydranencephaly, 605013 (3), Autosomal recessive"	Nde1 (MGI:1914453)			
chr16	15703134	15857031	16p13.13-p13.12	16p13.11		160745	"MYH11, AAT4, FAA4"	"Myosin, heavy polypeptide-11, smooth muscle"	MYH11	4629	ENSG00000133392	fused with CBFB by inversion in acute myelomonocytic leukemia	"Aortic aneurysm, familial thoracic 4, 132900 (3), Autosomal dominant"	Myh11 (MGI:102643)			
chr16	15865718	15888648	16p13.11	16p13.11		617149	"FOPNL, FOR20, C16orf63"	FGFR1OP N-terminal domain-like protein	FOPNL	123811	ENSG00000133393			Fopnl (MGI:1913336)			
chr16	15949576	16143073	16p13.1	16p13.11		158343	"ABCC1, MRP1, MRP"	"ATP-binding cassette, subfamily C, member 1 (multidrug resistance-associated protein 1)"	ABCC1	4363	ENSG00000103222			Abcc1 (MGI:102676)			
chr16	16149564	16223616	16p13.1	16p13.11		603234	"ABCC6, ARA, ABC34, MLP1, PXE, GACI2"	"ATP-binding cassette, subfamily C, member 6"	ABCC6	368	ENSG00000091262		"Arterial calcification, generalized, of infancy, 2, 614473 (3), Autosomal recessive; Pseudoxanthoma elasticum, 264800 (3), Autosomal recessive; Pseudoxanthoma elasticum, forme fruste, 177850 (3), Autosomal dominant"	Abcc6 (MGI:1351634)			
chr16	16232531	16294810	16p13.11	16p13.11		609159	NOMO3	Nodal modulator 3	NOMO3	408050	ENSG00000103226			Nomo1 (MGI:2385850)			
chr16	16700000	28500000	16p12			136570	"DEL16p12.1, C16DELp12.1"	"Chromosome 16p12.1 deletion syndrome, 520kb"				between 21.85-22.37 Mb	"Chromosome 16p12.1 deletion syndrome, 520kb, 136570 (4)"				
chr16	16700000	35300000	16p12-p11.2			608105	EPRPDC	"Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp"		574044		between D16S3133 and D16S3131	"Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp, 608105 (2), Autosomal recessive"				
chr16	16700000	28500000	16p12			611247	"MAFD4, BPAD"	Major affective disorder 4		100126593		max lod at D16S769	"Major affective disorder 4, 611247 (2)"				
chr16	16700000	28500000	16p12.3-p12.1			602594	RP22	Retinitis pigmentosa-22	RP22	6114			"Retinitis pigmentosa 22, 602594 (2)"				
chr16	17102323	17470880	16p13.1	16p12.3		608124	"XYLT1, XT1, DBQD2"	Xylosyltransferase 1	XYLT1	64131	ENSG00000103489		"Desbuquois dysplasia 2, 615777 (3), Autosomal recessive; {Pseudoxanthoma elasticum, modifier of severity of}, 264800 (3), Autosomal recessive"	Xylt1 (MGI:2451073)			
chr16	18499923	18562142	16p12.3	16p12.3		609158	NOMO2	Nodal modulator 2	NOMO2	283820	ENSG00000185164			Nomo1 (MGI:2385850)			
chr16	18782954	18790333	16p	16p12.3		603674	RPS15A	Ribosomal protein S15a	RPS15A	6210	ENSG00000134419			Rps15a (MGI:2389091)			
chr16	18791666	18801677	16p12-p11.2	16p12.3		607669	"ARL6IP1, KIAA0069, SPG61"	ADP-ribosylation factor-like 6 interacting protein 1	ARL6IP1	23204	ENSG00000170540	mutation identified in 1 family	"?Spastic paraplegia 61, autosomal recessive, 615685 (3), Autosomal recessive"	Arl6ip1 (MGI:1858943)			
chr16	18804852	18926427	16p12	16p12.3		607032	"SMG1, LIP, KIAA0421"	"SMG1, C. elegans, homolog of"	SMG1	23049	ENSG00000157106			Smg1 (MGI:1919742)			
chr16	18983933	19063941	16p12.3	16p12.3		617198	TMC7	Transmembrane channel-like protein 7	TMC7	79905	ENSG00000170537			Tmc7 (MGI:2443317)			
chr16	19067594	19080094	16p13.1-p12	16p12.3		601683	"COQ7, CLK1, COQ10D8"	"COQ7, S. cerevisiae, homolog of"	COQ7	10229	ENSG00000167186	mutation identified in 1 COQ10D8 patient	"?Coenzyme Q10 deficiency, primary, 8, 616733 (3), Autosomal recessive"	Coq7 (MGI:107207)			
chr16	19410538	19499112	16p12.3	16p12.3		617197	TMC5	Transmembrane channel-like protein 5	TMC5	79838	ENSG00000103534			Tmc5 (MGI:1921674)			
chr16	19501692	19522144	16p12-p11.2	16p12.3		605943	"GDE1, MIR16"	Glycerophosphodiester phosphodiesterase 1	GDE1	51573	ENSG00000006007			Gde1 (MGI:1891827)			
chr16	19523856	19553407	16p12.3	16p12.3		609544	"CCP110, CP110, KIAA0419"	"Centrosomal coiled-coil protein, 110kD"	CCP110	9738	ENSG00000103540			Ccp110 (MGI:2141942)			
chr16	19858970	19886044	16p12.3-p12.1	16p12.3		605948	"GPRC5B, RAIG2"	"G protein-coupled receptor, family C, group 5, member B"	GPRC5B	51704	ENSG00000167191			Gprc5b (MGI:1927596)			
chr16	20309573	20327804	16p12.3	16p12.3		602977	GP2	"Glycoprotein 2, zymogen granule membrane"	GP2	2813	ENSG00000169347	previously assigned to chr.9		Gp2 (MGI:1914383)			
chr16	20333050	20356300	16p12.3	16p12.3		191845	"UMOD, HNFJ1, FJHN, MCKD2, ADMCKD2"	"Uromodulin (uromucoid, Tamm-Horsfall glycoprotein)"	UMOD	7369	ENSG00000169344		"Glomerulocystic kidney disease with hyperuricemia and isosthenuria, 609886 (3); Hyperuricemic nephropathy, familial juvenile 1, 162000 (3), Autosomal dominant; Medullary cystic kidney disease 2, 603860 (3)"	Umod (MGI:102674)			
chr16	20409533	20441332	16p12.3	16p12.3		614361	ACSM5	"Acyl-CoA synthetase medium-chain family, member 5"	ACSM5	54988	ENSG00000183549			Acsm5 (MGI:2444086)			
chr16	20451460	20487668	16p12.3	16p12.3		614358	ACSM2A	"Acyl-CoA synthetase medium-chain family, member 2A"	ACSM2A	123876	ENSG00000183747			Acsm2 (MGI:2385289)			
chr16	20536757	20576375	16p12.3	16p12.3		614359	"ACSM2B, HXMA"	"Acyl-CoA synthetase medium-chain family, member 2B"	ACSM2B	348158	ENSG00000066813						
chr16	20623234	20697787	16p12.3	16p12.3		614357	"ACSM1, MACS1"	"Acyl-CoA synthetase medium-chain family, member 1"	ACSM1	116285	ENSG00000166743			Acsm1 (MGI:2152200)			
chr16	20730588	20741963	16p12.3	16p12.3		616662	THUMPD1	THUMP domain-containing protein 1	THUMPD1	55623	ENSG00000066654			Thumpd1 (MGI:2444479)			
chr16	20742439	20797810	16p13.11	16p12.3		145505	"ACSM3, SAH"	Acyl-CoA synthetase medium-chain family member 3	ACSM3	6296	ENSG00000005187		"{?Hypertension, essential} (1)"	Acsm3 (MGI:99538)			
chr16	20854924	20900357	16p12.3	16p12.3		616167	"DCUN1D3, SCCRO3"	DCN1 domain-containing protein 3	DCUN1D3	123879	ENSG00000188215			Dcun1d3 (MGI:2679003)			
chr16	20899625	20925005	16p12.3	16p12.3		614709	LYRM1	LYR motif-containing protein 1	LYRM1	57149	ENSG00000102897			Lyrm1 (MGI:1921169)			
chr16	20933110	21159536	16p12	16p12.3		603334	"DNAH3, DNAHC3B"	"Dynein, axonemal, heavy chain 3"	DNAH3	55567	ENSG00000158486			Dnah3 (MGI:2683040)			
chr16	21158348	21180615	16p12.3	16p12.3		611304	TMEM159	Transmembrane protein 159	TMEM159	57146	ENSG00000011638			Tmem159 (MGI:1925752)			
chr16	21197449	21214509	16p12	16p12.3-p12.2		182888	ZP2	Zona pellucida glycoprotein 2	ZP2	7783	ENSG00000103310			Zp2 (MGI:99214)			
chr16	21200000	35300000	16p12.2-p11.2			613604	"DEL16p12.1p11.2, C16DELp12.1p11.2"	Chromosome 16p12.2-p11.2 deletion syndrome				17.1-8.7 Mb contiguous gene deletion syndrome	"Chromosome 16p12.2-p11.2 deletion syndrome, 613604 (4), Isolated cases"				
chr16	21200000	52600000	16p12.2-q12.1			611096	"MRT10, MRT20"	611096	MRT10	100101425		"between rs724466 and rs3901517, rs7197568 and rs71972227"	"Mental retardation, autosomal recessive 10/20, 611096 (2), Autosomal recessive"				
chr16	21233694	21252428	16p12.2	16p12.2		609901	"ANKS4B, HARP, FLJ38819"	Ankyrin repeat and sterile alpha motif domain-containing protein 4B	ANKS4B	257629	ENSG00000175311			Anks4b (MGI:1919324)			
chr16	21258517	21303135	16p13.11-p12.3	16p12.2		123740	"CRYM, DFNA40"	"Crystallin, mu"	CRYM	1428	ENSG00000103316		"Deafness, autosomal dominant 40, 616357 (3), Autosomal dominant"	Crym (MGI:102675)			
chr16	21597220	21657472	16p12.2	16p12.2		609388	"METTL9, DREV"	Methyltransferase-like 9	METTL9	51108	ENSG00000197006			Mettl9 (MGI:1914862)			
chr16	21641283	21652665	16p13	16p12.2		606222	"IGSF6, DORA"	"Immunoglobulin superfamily, member 6"	IGSF6	10261	ENSG00000140749			Igsf6 (MGI:1891393)			
chr16	21664132	21762624	16p12.2	16p12.2		607038	"OTOA, DFNB22"	Otoancorin	OTOA	146183	ENSG00000155719		"Deafness, autosomal recessive 22, 607039 (3), Autosomal recessive"	Otoa (MGI:2149209)			
chr16	21953063	21983659	16p12	16p12.2		191329	"UQCRC2, MC3DN5"	Ubiquinol-cytochrome c reductase core protein II	UQCRC2	7385	ENSG00000140740		"Mitochondrial complex III deficiency, nuclear type 5, 615160 (3), Autosomal recessive"	Uqcrc2 (MGI:1914253)			
chr16	22206270	22288744	Chr.16	16p12.2		606968	EEF2K	Elongation factor 2 kinase	EEF2K	29904	ENSG00000103319			Eef2k (MGI:1195261)			
chr16	22297374	22335102	16p12.2	16p12.2		617815	"POLR3E, SIN, KIAA1452"	"Polymerase III, RNA, subunit E"	POLR3E	55718	ENSG00000058600			Polr3e (MGI:1349452)			
chr16	22345935	22374616	16p13.1-p12	16p12.2		117340	CDR2	"Cerebellar degeneration-related antigen-2, 62kD"	CDR2	1039	ENSG00000140743			Cdr2 (MGI:1100885)			
chr16	22814165	22916337	16p12	16p12.2		604056	"HS3ST2, 30ST2"	Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 2	HS3ST2	9956	ENSG00000122254			Hs3st2 (MGI:1333802)			
chr16	23182718	23216878	16p13-p12	16p12.2		600761	"SCNN1G, PHA1, BESC3"	"Sodium channel, nonvoltage-gated 1, gamma"	SCNN1G	6340	ENSG00000166828	same 400kb fragment as SCNN1B	"Bronchiectasis with or without elevated sweat chloride 3, 613071 (3), Autosomal dominant; Liddle syndrome, 177200 (3), Autosomal dominant; Pseudohypoaldosteronism, type I, 264350 (3), Autosomal recessive"	Scnn1g (MGI:104695)			
chr16	23278230	23381298	16p13-p12	16p12.2		600760	"SCNN1B, BESC1"	"Sodium channel, nonvoltage-gated 1, beta"	SCNN1B	6338	ENSG00000168447		"Bronchiectasis with or without elevated sweat chloride 1, 211400 (3), Autosomal dominant; Liddle syndrome, 177200 (3), Autosomal dominant; Pseudohypoaldosteronism, type I, 264350 (3), Autosomal recessive"	Scnn1b (MGI:104696)			
chr16	23388492	23453214	16p	16p12.2		606978	"COG7, CDG2E"	Component of oligomeric golgi complex 7	COG7	91949	ENSG00000168434		"Congenital disorder of glycosylation, type IIe, 608779 (3)"	Cog7 (MGI:2685013)			
chr16	23522012	23557374	16p13.1-p11.2	16p12.2		612799	"EARS2, KIAA1970, COXPD12"	Glutamyl-tRNA synthetase 2	EARS2	124454	ENSG00000103356		"Combined oxidative phosphorylation deficiency 12, 614924 (3), Autosomal recessive"	Ears2 (MGI:1914667)			
chr16	23581011	23596328	16p12.3-p12.1	16p12.2		603836	NDUFAB1	"NADH-ubiquinone oxidoreductase 1, alpha/beta subcomplex, 1"	NDUFAB1	4706	ENSG00000004779			"Ndufab1,Ndufab1-ps (MGI:1917566,MGI:4936891)"			
chr16	23603161	23641356	16p12	16p12.2		610355	"PALB2, FANCN, PNCA3"	Partner and localizer of BRCA2	PALB2	79728	ENSG00000083093		"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant; Fanconi anemia, complementation group N, 610832 (3); {Pancreatic cancer, susceptibility to, 3}, 613348 (3)"	Palb2 (MGI:3040695)			
chr16	23641365	23676206	16p12.2	16p12.2		612962	"DCTN5, p25"	Dynactin 5	DCTN5	84516	ENSG00000166847			Dctn5 (MGI:1891689)			
chr16	23678771	23690366	16p12.2	16p12.2		602098	"PLK1, STPK13"	Polo-like kinase 1	PLK1	5347	ENSG00000166851			Plk1 (MGI:97621)			
chr16	23690303	23713499	16p12.2	16p12.2		604034	ERN2	Endoplasmic reticulum-to-nucleus signaling 2	ERN2	10595	ENSG00000134398			Ern2 (MGI:1349436)			
chr16	23835978	24220610	16p11.2	16p12.2-p12.1		176970	"PRKCB1, PKCB"	"Protein kinase C, beta 1 polypeptide"	PRKCB	5579	ENSG00000166501			Prkcb (MGI:97596)			
chr16	24200000	35300000	16p12.1-p11.2			157700	"MMVP1, MVP, PMV"	"Mitral valve prolapse, myxomatous 1"	MMVP1	50951			"Mitral valve prolapse, myxomatous 1, 157700 (2), Autosomal dominant"				
chr16	24255552	24362415	16p13.1-p12	16p12.1		606403	CACNG3	"Calcium channel, voltage-dependent, gamma-3 subunit"	CACNG3	10368	ENSG00000006116			Cacng3 (MGI:1859165)			
chr16	24539586	24572862	16p12-p11.2	16p12.1		600938	RBBP6	Retinoblastoma-binding protein-6	RBBP6	5930	ENSG00000122257			Rbbp6 (MGI:894835)			
chr16	24610208	24826226	16p12	16p12.1		610739	"TNRC6A, GW182, KIAA1460"	Trinucleotide repeat-containing gene 6A	TNRC6A	27327	ENSG00000090905			Tnrc6a (MGI:2385292)			
chr16	24845862	24911627	16p12.1	16p12.1		610238	"SLC5A11, KST1, SGLT6, SMIT2"	"Solute carrier family 5 (sodium/glucose cotransporter), member 11"	SLC5A11	115584	ENSG00000158865			Slc5a11 (MGI:1919316)			
chr16	24919383	25015600	16p12.2	16p12.1		608293	"ARHGAP17, RICH1"	RHO GTPase-activating protein 17	ARHGAP17	55114	ENSG00000140750			Arhgap17 (MGI:1917747)			
chr16	25111701	25178230	16p12.3-p12.1	16p12.1		610286	LCMT1	Leucine carboxyl methyltransferase 1	LCMT1	51451	ENSG00000205629			Lcmt1 (MGI:1353593)			
chr16	25216916	25228931	16p12-p11.2	16p12.1		603750	AQP8	Aquaporin 8	AQP8	343	ENSG00000103375			Aqp8 (MGI:1195271)			
chr16	25692025	26137687	16p11.2	16p12.1		604059	"HS3ST4, 30ST4"	Heparan sulfate D-glucosaminyl 3-O-sulfotransferase 4	HS3ST4	9951	ENSG00000182601			Hs3st4 (MGI:1333792)			
chr16	27203485	27222304	16p12.1	16p12.1		611917	JMJD5	Jumonji domain-containing protein 5	KDM8	79831	ENSG00000155666			Kdm8 (MGI:1924285)			
chr16	27224993	27268791	16p12.1	16p12.1		617263	"NSMCE1, NSE1"	"Non-SMC element 1, S. cerevisiae, homolog of"	NSMCE1	197370	ENSG00000169189			Nsmce1 (MGI:1914961)			
chr16	27313667	27364777	16p12.1-p11.2	16p12.1		147781	"IL4R, IL4RA"	Interleukin-4 receptor	IL4R	3566	ENSG00000077238		"{AIDS, slow progression to}, 609423 (3); {Atopy, susceptibility to}, 147050 (3), Autosomal dominant"	Il4ra (MGI:105367)			
chr16	27402161	27452042	16p11	16p12.1		605383	"IL21R, IMD56"	Interleukin 21 receptor	IL21R	50615	ENSG00000103522	fusion partner with BCL6	"[IgE, elevated level of], 147050 (3), Autosomal dominant; Immunodeficiency 56, 615207 (3), Autosomal recessive"	Il21r (MGI:1890475)			
chr16	27460612	27549929	16p12.1	16p12.1		603246	GTF3C1	"General transcription factor 3C, polypeptide 1"	GTF3C1	2975	ENSG00000077235			Gtf3c1 (MGI:107887)			
chr16	27550127	27780370	16p12.1	16p12.1		616650	"KATNIP, KIAA0556"	Katanin-interacting protein	KIAA0556	23247	ENSG00000047578		"Joubert syndrome 26, 616784 (3), Autosomal recessive"	D430042O09Rik (MGI:2442760)			
chr16	27787528	28063508	16p12.1	16p12.1		617161	GSG1L	GSG1-like protein	GSG1L	146395	ENSG00000169181			Gsg1l (MGI:2685483)			
chr16	28097975	28212030	16p12.1	16p12.1		608411	"XPO6, EXP6, KIAA0370"	Exportin 6	XPO6	23214	ENSG00000169180			Xpo6 (MGI:2429950)			
chr16	28466652	28492301	16p12.1	16p12.1		607042	"CLN3, BTS"	Battenin	CLN3	1201	ENSG00000188603		"Ceroid lipofuscinosis, neuronal, 3, 204200 (3), Autosomal recessive"	Cln3 (MGI:107537)			
chr16	28494648	28498969	16p11.2	16p12.1		605220	"APOBR, APOB48R"	Apolipoprotein B receptor	APOBR	55911	ENSG00000184730			Apobr (MGI:2176230)			
chr16	28499361	28526729	16p11	16p12.1-p11.2		608273	"IL27, IL30"	Interleukin 27	IL27	246778	ENSG00000197272			Il27 (MGI:2384409)			
chr16	28500000	35300000	16p11.2			613444	"BMIQ16, DEL16p.11.2, C16DELp11.2"	"Chromosome 16p11.2 deletion syndrome, 220kb"					"[Body mass index QTL16], 613444 (4); Chromosome 16p11.2 deletion syndrome, 220kb, 613444 (4)"				
chr16	28500000	35300000	16p11.2			611913	"DEL16p11.2, C16DELp11.2, AUTS14A"	"Chromosome 16p11.2 deletion syndrome, 593kb"					"{Autism susceptibility 14A}, 611913 (2); Chromosome 16p11.2 deletion syndrome, 593kb, 611913 (4)"				
chr16	28500000	35300000	16p11.2			614671	"DUP16p11.2, C16DUPp11.2, AUTS14B"	Chromosome 16p11.2 duplication syndrome					"{Autism, susceptibility to, 14B}, 614671 (2); Chromosome 16p11.2 duplication syndrome, 614671 (4)"				
chr16	28500000	36800000	16p11			615835	INV16p11	Chromosome 16p11 inversion (0.45Mb)									
chr16	28537340	28539173	16p11.2	16p11.2		614812	"NUPR1, COM1, p8"	"Nuclear protein, transcriptional regulator, 1"	NUPR1	26471	ENSG00000176046			Nupr1 (MGI:1891834)			
chr16	28553914	28591789	16p11.2	16p11.2		613374	"CCDC101, STAF36"	Coiled-coil domain-containing protein 101	SGF29	112869	ENSG00000176476			Sgf29 (MGI:1922815)			
chr16	28591942	28597085	16p12.1-p11.2	16p11.2		601292	"SULT1A2, STP2"	"Sulfotransferase family 1A, phenol-preferring, member 2"	SULT1A2	6799	ENSG00000197165	45kb from STP1					
chr16	28605586	28623585	16p12.1-p11.2	16p11.2		171150	"SULT1A1, STP1, STP, PST"	"Sulfotransferase family 1A, phenol-preferring, member 1"	SULT1A1	6817	ENSG00000196502						
chr16	28688557	28735729	16p11.2	16p11.2		603916	"EIF3C, EIF3S8"	"Eukaryotic translation initiation factor 3, subunit C"	EIF3C	8663	ENSG00000184110			Eif3c (MGI:1926966)			
chr16	28823047	28837236	16p11	16p11.2		607931	"ATXN2L, A2D"	Ataxin 2-like	ATXN2L	11273	ENSG00000168488	pseudogene at 7p21		Atxn2l (MGI:2446242)			
chr16	28842410	28859561	16p11.2	16p11.2		602389	"TUFM, EFTU, COXPD4"	"Tu translation elongation factor, mitochondrial"	TUFM	7284	ENSG00000178952	pseudogene on chr.17	"Combined oxidative phosphorylation deficiency 4, 610678 (3), Autosomal recessive"	Tufm (MGI:1923686)			
chr16	28846599	28874212	16p11.2	16p11.2		608937	"SH2B1, SH2B, KIAA1299"	SH2B adaptor protein 1	SH2B1	25970	ENSG00000178188			Sh2b1 (MGI:1201407)			
chr16	28878487	28904508	16p12	16p11.2		108730	"ATP2A1, SERCA1"	"ATPase, Ca++ transporting, fast-twitch, 1"	ATP2A1	487	ENSG00000196296		"Brody myopathy, 601003 (3), Autosomal recessive"	Atp2a1 (MGI:105058)			
chr16	28904420	28925210	16p11.2	16p11.2		611869	RABEP2	RAB GTPase-binding effector protein 2	RABEP2	79874	ENSG00000177548			Rabep2 (MGI:1917564)			
chr16	28931734	28939346	16p11.2	16p11.2		107265	"CD19, CVID3"	CD19 antigen	CD19	930	ENSG00000177455		"Immunodeficiency, common variable, 3, 613493 (3), Autosomal recessive"	Cd19 (MGI:88319)			
chr16	28950991	28966464	16p11.2	16p11.2		614525	"NFATC2IP, NIP45"	NFATC2-interacting protein	NFATC2IP	84901	ENSG00000176953			Nfatc2ip (MGI:1329015)			
chr16	28973998	28984768	16p11.2	16p11.2		612583	"SPNS1, SPIN1"	"Spinster, Drosophila, homolog of, 1"	SPNS1	83985	ENSG00000169682			Spns1 (MGI:1920908)			
chr16	28984825	28990782	16p11.2	16p11.2		602354	"LAT, IMD52"	Linker for activation of T cells	LAT	27040	ENSG00000213658		"Immunodeficiency 52, 617514 (3), Autosomal recessive"	Lat (MGI:1342293)			
chr16	29453587	29454963	16p11.2	16p11.2		613182	BOLA2	"BolA, E. coli, homolog of, 2"	BOLA2	552900	ENSG00000183336						
chr16	29454500	29458223	16p11.2	16p11.2		615823	"SLX1B, GIYD2"	"SLX1 structure-specific endonuclease subunit, S. cerevisiae, homolog of, B"	SLX1B	79008	ENSG00000181625			Slx1b (MGI:1915220)			
chr16	29459885	29464979	16p11.2	16p11.2		615819	SULT1A4	"Sulfotransferase family 1A, cytosolic, phenol-preferring, member 4"	SULT1A4	445329	ENSG00000213648						
chr16	29662949	29670875	16p11.2	16p11.2		182160	"SPN, LSN, CD43"	Sialophorin (leukosialin)	SPN	6693	ENSG00000197471			Spn (MGI:98384)			
chr16	29670587	29698698	16p11.2	16p11.2		606248	QPRT	Quinolinate phosphoribosyltransferase	QPRT	23475	ENSG00000103485			Qprt (MGI:1914625)			
chr16	29760803	29781647	16p11.2	16p11.2		617311	"ZG16, ZG16A, JCLN1"	"Zymogen granule protein, 16-kD"	ZG16	653808	ENSG00000174992			Zg16 (MGI:1916286)			
chr16	29790712	29805542	16p11.2	16p11.2		603213	"KIF22, KNSL4, KID, OBP, SEMDJL2"	Kinesin family member 22	KIF22	3835	ENSG00000079616		"Spondyloepimetaphyseal dysplasia with joint laxity, type 2, 603546 (3), Autosomal dominant"	Kif22 (MGI:109233)			
chr16	29806080	29811182	16p11.2	16p11.2		600999	"MAZ, ZF87, PUR1"	MYC-associated zinc finger protein	MAZ	4150	ENSG00000103495			Maz (MGI:1338823)			
chr16	29812087	29815919	16p11.2	16p11.2		614386	"PRRT2, PKC, DYT10, EKD1, BFIS2, BFIC2, ICCA"	Proline-rich transmembrane protein 2	PRRT2	112476	ENSG00000167371		"Convulsions, familial infantile, with paroxysmal choreoathetosis, 602066 (3), Autosomal dominant; Episodic kinesigenic dyskinesia 1, 128200 (3), Autosomal dominant; Seizures, benign familial infantile, 2, 605751 (3), Autosomal dominant"	Prrt2 (MGI:1916267)			
chr16	29816206	29822494	16p11.2	16p11.2		612033	"PAGR1, C16orf53, PA1"	PAXIP1-associated glutamate-rich protein 1	PAGR1	79447	ENSG00000280789			Pagr1a (MGI:1914528)			
chr16	29820393	29848038	16p13.1-p11.2	16p11.2		605088	"MVP, LRP"	"Major vault protein, rat, homolog of"	MVP	9961	ENSG00000013364			Mvp (MGI:1925638)			
chr16	29871158	29899572	16p11.2	16p11.2		616667	"SEZ6L2, BSRPA"	SEZ6-like protein 2	SEZ6L2	26470	ENSG00000174938			Sez6l2 (MGI:2385295)			
chr16	29906334	29926231	16p11.2	16p11.2		608947	"KCTD13, POLDIP1, FKSG86"	Potassium channel tetramerization domain-containing 13	KCTD13	253980	ENSG00000174943			Kctd13 (MGI:1923739)			
chr16	29973866	29992260	16p13.1-p12	16p11.2		613199	"TAOK2, TAO2, KIAA0881, PSK, PSK1"	Tao kinase 2	TAOK2	9344	ENSG00000149930			Taok2 (MGI:1915919)			
chr16	29992320	29996095	16p11.2	16p11.2		603365	HIRIP3	HIRA-interacting protein 3	HIRIP3	8479	ENSG00000149929			Hirip3 (MGI:2142364)			
chr16	30005513	30023279	16p11.2	16p11.2		604567	DOC2A	"Double C2-like domain-containing protein, alpha"	DOC2A	8448	ENSG00000149927			Doc2a (MGI:109446)			
chr16	30024422	30053025	16p11.2	16p11.2		615175	FAM57B	"Family with sequence similarity 57, member B"	FAM57B	83723	ENSG00000149926			Fam57b (MGI:1916202)			
chr16	30053089	30070419	16p11.2	16p11.2		103850	"ALDOA, GSD12"	"Aldolase A, fructose-bisphosphatase"	ALDOA	226	ENSG00000149925	pseudogenes on 3 and 10	"Glycogen storage disease XII, 611881 (3), Autosomal recessive"	Aldoa (MGI:87994)			
chr16	30075975	30085376	16p12-p11	16p11.2		602035	"PPP4C, PP4, PPX"	"Protein phosphatase 4, catalytic subunit"	PPP4C	5531	ENSG00000149923			Ppp4c (MGI:1891763)			
chr16	30085792	30091926	16p11.2	16p11.2		602427	"TBX6, SCDO5"	T-box 6	TBX6	6911	ENSG00000149922		"Spondylocostal dysostosis 5, 122600 (3), Autosomal recessive, Autosomal dominant"	Tbx6 (MGI:102539)			
chr16	30092313	30096215	16p11.2	16p11.2		609724	YPEL3	Yippee-like 3	YPEL3	83719	ENSG00000090238			Ypel3 (MGI:1913340)			
chr16	30104809	30113556	16p11.2	16p11.2		616318	"GDPD3, GDE7"	Glycerophosphodiester phosphodiesterase domain-containing protein 3	GDPD3	79153	ENSG00000102886			Gdpd3 (MGI:1915866)			
chr16	30114104	30123308	16p11.2	16p11.2		601795	"MAPK3, PRKM3, ERK1"	Mitogen-activated protein kinase 3	MAPK3	5595	ENSG00000102882			Mapk3 (MGI:1346859)			
chr16	30183409	30189075	16p11.2	16p11.2		605000	"CORO1A, TACO, CLIPINA, IMD8"	Coronin 1A	CORO1A	11151	ENSG00000102879		"Immunodeficiency 8, 615401 (3), Autosomal recessive"	Coro1a (MGI:1345961)			
chr16	30193842	30197565	16p11.2	16p11.2		615822	"SLX1A, GIYD1"	"SLX1 structure-specific endonuclease subunit, S. cerevisiae, homolog of, A"	SLX1A	548593	ENSG00000132207			Slx1b (MGI:1915220)			
chr16	30199227	30204328	16p11.2	16p11.2		600641	"SULT1A3, STM"	"Sulfotransferase family 1A, phenol-preferring, member 3"	SULT1A3	6818	ENSG00000261052						
chr16	30350765	30355360	16p11.2	16p11.2		604470	CD2BP2	CD2 antigen-binding protein 2	CD2BP2	10421	ENSG00000169217			Cd2bp2 (MGI:1917483)			
chr16	30357100	30370465	16p11.2	16p11.2		613620	TBC1D10B	"TBC1 domain family, member 10B"	TBC1D10B	26000	ENSG00000169221			Tbc1d10b (MGI:1915699)			
chr16	30370933	30377990	16p11.2	16p11.2		617378	"MYLPF, MLC2B, MRLC2, MYL11"	"Myosin light chain, phosphorylatable, fast skeletal muscle"	MYLPF	29895	ENSG00000180209			Mylpf (MGI:97273)			
chr16	30378132	30382849	16p11.2	16p11.2		612897	"SEPT1, DIFF6"	Septin 1	1-Sep	1731	ENSG00000180096			Sept1 (MGI:1858916)			
chr16	30423697	30430051	16p11.2	16p11.2		615840	DCTPP1	dCTP pyrophosphatase 1	DCTPP1	79077	ENSG00000179958			Dctpp1 (MGI:1913672)			
chr16	30443624	30445974	16p11.2	16p11.2		606218	"SEPHS2, SPS2"	Selenophosphate synthetase 2	SEPHS2	22928	ENSG00000179918			Sephs2 (MGI:108388)			
chr16	30472661	30523184	16p11.2	16p11.2		153370	"ITGAL, CD11A, LFA1A"	"Integrin, alpha-L (antigen CD11A (p180), lymphocyte function-associated antigen-1, alpha polypeptide)"	ITGAL	3683	ENSG00000005844			Itgal (MGI:96606)			
chr16	30650701	30656439	16p11.2	16p11.2		617423	PRR14	Proline-rich protein 14	PRR14	78994	ENSG00000156858			Prr14 (MGI:2384565)			
chr16	30658430	30670809	16p11.2	16p11.2		608601	"FBRS, FBS1"	Fibrosin	FBRS	64319	ENSG00000156860			Fbrs (MGI:104648)			
chr16	30699140	30740128	16p11.2	16p11.2		611421	"SRCAP, SWR1, KIAA0309, FLHS"	SNF2-related CBP activator protein	SRCAP	10847	ENSG00000080603		"Floating-Harbor syndrome, 136140 (3), Autosomal dominant"	Srcap (MGI:2444036)			
chr16	30748298	30761175	16p12.1-p11.2	16p11.2		172471	"PHKG2, GSD9C"	"Phosphorylase kinase, gamma 2 (testis/liver)"	PHKG2	5261	ENSG00000156873		"Cirrhosis due to liver phosphorylase kinase deficiency (3); Glycogen storage disease IXc, 613027 (3), Autosomal recessive"	Phkg2 (MGI:1916211)			
chr16	30761611	30800230	16p11.2	16p11.2		607700	"RNF40, BRE1B, RBP95, KIAA0661"	Ring finger protein 40	RNF40	9810	ENSG00000103549			Rnf40 (MGI:2142048)			
chr16	30834040	30894715	16p11	16p11.2		605847	BCL7C	B-cell CLL/lymphoma 7C	BCL7C	9274	ENSG00000099385			Bcl7c (MGI:1332237)			
chr16	30895823	30903559	16p11.2-p11.1	16p11.2		600435	"CTF1, CT1"	Cardiotrophin 1	CTF1	1489	ENSG00000150281			Ctf1 (MGI:105115)			
chr16	30923054	30948782	16p11.2	16p11.2		609085	"FBXL19, FBL19"	F-box and leucine-rich repeat protein 19	FBXL19	54620	ENSG00000099364			Fbxl19 (MGI:3039600)			
chr16	30949083	30954937	16p11.2	16p11.2		610930	"ORAI3, TMEM142C"	ORAI calcium release-activated calcium modulator 3	ORAI3	93129	ENSG00000175938			Orai3 (MGI:3039586)			
chr16	30956617	30984663	16p11.2	16p11.2		611052	"SETD1A, SET1A, SET1, KIAA0339"	SET domain-containing protein 1A	SETD1A	9739	ENSG00000099381			Setd1a (MGI:2446244)			
chr16	30985188	30989151	16p12-p11.2	16p11.2		607764	"HSD3B7, CBAS1"	3-beta-hydroxy-delta-5-C27-steroid oxidoreductase	HSD3B7	80270	ENSG00000099377		"Bile acid synthesis defect, congenital, 1, 607765 (3), Autosomal recessive"	Hsd3b7 (MGI:2141879)			
chr16	30989255	31010637	16p11.2	16p11.2		601485	"STX1B, GEFSP9"	Syntaxin 1B	STX1B	112755	ENSG00000099365		"Generalized epilepsy with febrile seizures plus, type 9, 616172 (3), Autosomal dominant"	Stx1b (MGI:1930705)			
chr16	31033094	31040167	16p11.2	16p11.2		186591	"STX4, STX4A"	Syntaxin 4	STX4	6810	ENSG00000103496			Stx4a (MGI:893577)			
chr16	31060842	31074319	16p11.2	16p11.2		617103	ZNF668	Zinc finger protein 668	ZNF668	79759	ENSG00000167394			Zfp668 (MGI:2442943)			
chr16	31083423	31089651	16p11.2	16p11.2		610561	"PRSS53, POL3S"	"Protease, serine, 53"	PRSS53	339105	ENSG00000151006			Prss53 (MGI:2652890)			
chr16	31090841	31094998	16p11.2	16p11.2		608547	"VKORC1, VKOR, VKCFD2, FLJ00289"	"Vitamin K epoxide reductase complex, subunit 1"	VKORC1	79001	ENSG00000167397		"Vitamin K-dependent clotting factors, combined deficiency of, 2, 607473 (3); Warfarin resistance, 122700 (3), Autosomal dominant"	Vkorc1 (MGI:106442)			
chr16	31108293	31117650	16p11.2	16p11.2		614901	"BCKDK, BDK, BCKDKD"	Branched-chain alpha-keto acid dehydrogenase kinase	BCKDK	10295	ENSG00000103507		"Branched-chain ketoacid dehydrogenase kinase deficiency, 614923 (3)"	Bckdk (MGI:1276121)			
chr16	31117663	31131392	16p11.2	16p11.2		609912	"KAT8, MYST1, MOF"	K(lysine) acetyltransferase 8	KAT8	84148	ENSG00000103510			Kat8 (MGI:1915023)			
chr16	31131432	31135761	16p11.2	16p11.2		600823	PRSS8	"Protease, serine, 8 (prostasin)"	PRSS8	5652	ENSG00000052344			Prss8 (MGI:1923810)			
chr16	31138925	31150093	16p11.2	16p11.2		610560	PRSS36	"Protease, serine, 36"	PRSS36	146547	ENSG00000178226			Prss36 (MGI:1924863)			
chr16	31180109	31194870	16p11.2	16p11.2		137070	"FUS, TLS, ALS6, ETM4"	"Fusion, derived from 12-16 translocation, malignant liposarcoma"	FUS	2521	ENSG00000089280	"fused with DDIT3 in myxoid liposarcoma, with ERG in leukemia, and ATF1 in angiomatoid fibrous histiocytoma"	"Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia, 608030 (3); Essential tremor, hereditary, 4, 614782 (3), Autosomal dominant"				
chr16	31201485	31202775	16p12-p11.2	16p11.2		606838	"PYCARD, TMS1, ASC"	PYD and CARD domain-containing protein (target of methylation-induced silencing 1)	PYCARD	29108	ENSG00000103490			Pycard (MGI:1931465)			
chr16	31214020	31225655	16p11.2	16p11.2		613288	"TRIM72, MG53"	Tripartite motif-containing protein 72	TRIM72	493829	ENSG00000177238			Trim72 (MGI:3612190)			
chr16	31215961	31217092	16p12.1	16p11.2		615700	"PYDC1, POP1, PYC1, ASC2"	Pyrin domain-containing protein 1	PYDC1	260434	ENSG00000169900						
chr16	31259966	31332891	16p11.2	16p11.2		120980	"ITGAM, CR3A, CD11B, MAC1A, SLEB6"	"Integrin, alpha-M (complement component receptor-3, alpha; antigen CD11B (p170); macrophage antigen, alpha polypeptide)"	ITGAM	3684	ENSG00000169896	?in same restriction fragment as LFA1A	"{Systemic lupus erythematous, association with susceptibility to, 6}, 609939 (3)"	Itgam (MGI:96607)			
chr16	31355133	31382996	16p11.2	16p11.2		151510	"ITGAX, CD11C"	"Integrin, alpha-X (antigen CD11C (p150), alpha polypeptide)"	ITGAX	3687	ENSG00000140678			Itgax (MGI:96609)			
chr16	31393222	31426512	16p11.2	16p11.2		602453	"ITGAD, CD11D"	"Integrin, alpha D"	ITGAD	3681	ENSG00000156886			Itgad (MGI:3578624)			
chr16	31427730	31428427	16p11.2	16p11.2		602009	COX6A2	"Cytochrome c oxidase, subunit 6A2"	COX6A2	1339	ENSG00000156885			Cox6a2 (MGI:104649)			
chr16	31458272	31467166	16p11.2	16p11.2		615549	"ARMC5, AIMAH2"	Armadillo repeat-containing protein 5	ARMC5	79798	ENSG00000140691		"ACTH-independent macronodular adrenal hyperplasia 2, 615954 (3), Autosomal dominant, Somatic mutation"	Armc5 (MGI:2384586)			
chr16	31472154	31477959	16p11.2	16p11.2		602353	"TGFB1I1, ARA55, HIC5"	"Transforming growth factor, beta-1-induced 1"	TGFB1I1	7041	ENSG00000140682			Tgfb1i1 (MGI:102784)			
chr16	31482534	31490769	16p11.2	16p11.2		182381	"SLC5A2, SGLT2"	"Solute carrier family 5 (sodium/glucose cotransporter), member 2"	SLC5A2	6524	ENSG00000140675		"Renal glucosuria, 233100 (3), Autosomal recessive, Autosomal dominant"	Slc5a2 (MGI:2181411)			
chr16	31527851	31528803	16p11.2	16p11.2		605821	"ERAF, EDRF, AHSP"	Erythroid-associated factor (alpha-hemoglobin stabilizing protein)	AHSP	51327	ENSG00000169877						
chr16	31873757	31917950	Chr.16	16p11.2		604752	"ZNF267, HZF2"	Zinc finger protein-167	ZNF267	10308	ENSG00000185947			D3Ertd254e (MGI:1098769)			
chr16	32673527	32678620	16p13	16p11.2		617482	TP53TG3	TP53 target gene 3	TP53TG3	24150	ENSG00000183632						
chr16	36800000	74100000	16q11-q22			610753	AA2	Alopecia areata 2		100034703		max lod at D16S415	"Alopecia areata 2, 610753 (2), Autosomal recessive, Autosomal dominant"				
chr16	36800000	74100000	16q11.1-q22			126900	DUPC1	Dupuytren contracture 1		780895		max lod at D16S415	"Dupuytren contracture 1, 126900 (2), Autosomal dominant"				
chr16	36800000	90338345	16q			610707	PSORS8	Psoriasis susceptibility 8	PSORS8	140454		proximal to D16S3034	"{Psoriasis susceptibility 8}, 610707 (2)"				
chr16	36800000	90338345	16q			606711	SLI1	"Specific language impairment QTL, 1"		171013			"Specific language impairment QTL, 1, 606711 (2), Multifactorial"				
chr16	36800000	90338345	16q			194090	WT3	Wilms tumor-3		8136		loss of heterozygosity	"Wilms tumor, type 3, 194090 (2), Autosomal dominant"				
chr16	46578590	46621401	16q11.2	16q11.2		611027	"SHCBP1, PAL"	SHC SH2 domain-binding protein 1	SHCBP1	79801	ENSG00000171241			Shcbp1 (MGI:1338802)			
chr16	46657978	46689231	16q11.2	16q11.2		601501	"VPS35, MEM3, PARK17"	"Vacuolar protein sorting 35, yeast, homolog of"	VPS35	55737	ENSG00000069329		"{Parkinson disease 17}, 614203 (3), Autosomal dominant"	Vps35 (MGI:1890467)			
chr16	46689645	46698393	16q12	16q11.2		607213	"ORC6, ORC6L"	"Origin recognition complex, subunit 6, S. cerevisiae, homolog of"	ORC6	23594	ENSG00000091651		"Meier-Gorlin syndrome 3, 613803 (3), Autosomal recessive"	Orc6 (MGI:1929285)			
chr16	46702281	46763245	16q11.2	16q11.2		612147	"MYLK3, MLCK"	Myosin light chain kinase 3	MYLK3	91807	ENSG00000140795			Mylk3 (MGI:2443063)			
chr16	46884379	46931296	16q12.1	16q11.2		138210	"GPT2, ALT2, MRT49"	Glutamate pyruvate transaminase 2	GPT2	84706	ENSG00000166123		"Mental retardation, autosomal recessive 49, 616281 (3), Autosomal recessive"	Gpt2 (MGI:1915391)			
chr16	46955361	46973713	16q12.1	16q11.2		611322	"DNAJA2, DJ3, CPR3"	"DNAJ/HSP40 homolog, subfamily A, member 2"	DNAJA2	10294	ENSG00000069345			Dnaja2 (MGI:1931882)			
chr16	47000000	52600000	16q12.1			602639	"STHAG2, HYD2"	"Tooth agenesis, selective, 2"	HYD2	8137			"Tooth agenesis, selective, 2, 602639 (2)"				
chr16	47000000	79200000	16q12.1-q23.1			614668	STUT4	"Stuttering, familial persistent, 4"		100909385		max lod at D16S3043	"Stuttering, familial persistent, 4, 614668 (2)"				
chr16	47081519	47144024	16q11	16q12.1		607974	NEOT2	Neuropilin and tolloid like 2	NETO2	81831	ENSG00000171208			Neto2 (MGI:1921763)			
chr16	47154386	47461273	16q12.1	16q12.1		611803	"ITFG1, TIP"	Integrin-alpha FG-gap repeat-containing protein 1	ITFG1	81533	ENSG00000129636			Itfg1 (MGI:106419)			
chr16	47461130	47701522	16q12-q13	16q12.1		172490	PHKB	"Phosphorylase kinase, beta polypeptide"	PHKB	5257	ENSG00000102893		"Phosphorylase kinase deficiency of liver and muscle, autosomal recessive, 261750 (3), Autosomal recessive"	Phkb (MGI:97578)			
chr16	48082972	48146769	16q12.1	16q12.1		607041	"ABCC12, MRP9"	"ATP-binding cassette, subfamily C, member 12"	ABCC12	94160	ENSG00000140798			Abcc12 (MGI:2441679)			
chr16	48164841	48249972	16q12.1	16q12.1		607040	"ABCC11, MRP8, EWWD, WW"	"ATP-binding cassette, subfamily C, member 11"	ABCC11	85320	ENSG00000121270		"[Axillary odor, variation in], 117800 (3), Autosomal dominant; [Colostrum secretion, variation in], 117800 (3), Autosomal dominant; [Earwax, wet/dry], 117800 (3), Autosomal dominant"				
chr16	48244166	48362998	16q12.1	16q12.1		617774	"LONP2, PLON, PSLON"	"LON peptidase 2, peroxisomal"	LONP2	83752	ENSG00000102910			Lonp2 (MGI:1914137)			
chr16	48354580	48448434	16q12	16q12.1		602212	SIAH1	"Seven in absentia, Drosophila, homolog of, 1"	SIAH1	6477	ENSG00000196470			Siah1a (MGI:108064)			
chr16	49277916	49281830	16q12.1	16q12.1		600432	CLN1	Precerebellin 1	CBLN1	869	ENSG00000102924			Cbln1 (MGI:88281)			
chr16	49487530	49857918	16q12	16q12.1		604557	"ZNF423, ZFP423, OAZ, KIAA0760, NPHP14, JBTS19"	Zinc finger protein 423	ZNF423	23090	ENSG00000102935		"Joubert syndrome 19, 614844 (3), Autosomal recessive, Autosomal dominant; Nephronophthisis 14, 614844 (3), Autosomal recessive, Autosomal dominant"	Zfp423 (MGI:1891217)			
chr16	50025205	50037087	16q12.1	16q12.1		616869	"CNEP1R1, NEP1R1, TMEM188"	C-terminal domain nuclear envelope phosphatase 1 regulatory subunit 1	CNEP1R1	255919	ENSG00000205423			Cnep1r1 (MGI:1921981)			
chr16	50065940	50107271	16q12.1	16q12.1		614951	"HEATR3, SYO1"	HEAT repeat-containing protein 3	HEATR3	55027	ENSG00000155393			Heatr3 (MGI:2444491)			
chr16	50246137	50318134	16q12-q13	16q12.1		600385	ADCY7	Adenylate cyclase-7	ADCY7	113	ENSG00000121281			Adcy7 (MGI:102891)			
chr16	50548329	50649248	16q12	16q12.1		607851	NKD1	"Naked cuticle, Drosophila, homolog of, 1"	NKD1	85407	ENSG00000140807			Nkd1 (MGI:2135954)			
chr16	50666299	50681352	16q12.1	16q12.1		613281	"SNX20, SLIC1"	Sorting nexin 20	SNX20	124460	ENSG00000167208			Snx20 (MGI:1918857)			
chr16	50693586	50733076	16q12	16q12.1		605956	"NOD2, CARD15, IBD1, CD, YAOS, BLAUS"	Nucleotide-binding oligomerization domain protein 2	NOD2	64127	ENSG00000167207		"Blau syndrome, 186580 (3), Autosomal dominant; {Inflammatory bowel disease 1, Crohn disease}, 266600 (3), Multifactorial; {Psoriatic arthritis, susceptibility to}, 607507 (2); {Yao syndrome}, 617321 (3), Multifactorial"	Nod2 (MGI:2429397)			
chr16	50742025	50801934	16q12-q13	16q12.1		605018	"CYLD, CDMT, EAC, MFT1, KIAA0849, BRSS"	CYLD gene	CYLD	1540	ENSG00000083799	behaves as tumor suppressor	"Brooke-Spiegler syndrome, 605041 (3), Autosomal dominant; Cylindromatosis, familial, 132700 (3), Autosomal dominant; Trichoepithelioma, multiple familial, 1, 601606 (3), Autosomal dominant"	Cyld (MGI:1921506)			
chr16	51135974	51151271	16q12.1	16q12.1		602218	"SALL1, HSAL1, TBS"	Sal-like 1	SALL1	6299	ENSG00000103449		"Townes-Brocks branchiootorenal-like syndrome, 107480 (3), Autosomal dominant; Townes-Brocks syndrome 1, 107480 (3), Autosomal dominant"	Sall1 (MGI:1889585)			
chr16	53054981	53327501	16q12.2	16q12.2		616936	"CHD9, CREMM, PRIC320, KIAA0308"	Chromodomain helicase DNA-binding protein 9	CHD9	80205	ENSG00000177200			Chd9 (MGI:1924001)			
chr16	53434419	53491647	16q12.2	16q12.2		180203	RBL2	Retinoblastoma-like 2	RBL2	5934	ENSG00000103479			Rbl2 (MGI:105085)			
chr16	53491039	53504410	16q12.2	16q12.2		608483	"AKTIP, FTS, FT1"	AKT_interacting protein	AKTIP	64400	ENSG00000166971			Aktip (MGI:3693832)			
chr16	53599238	53703937	16q12.2	16q12.2		610937	"RPGRIP1L, KIAA1005, JBTS7, MKS5"	RPGRIP1-like	RPGRIP1L	23322	ENSG00000103494		"COACH syndrome, 216360 (3), Autosomal recessive; Joubert syndrome 7, 611560 (3), Autosomal recessive; Meckel syndrome 5, 611561 (3), Autosomal recessive"	Rpgrip1l (MGI:1920563)			
chr16	53703962	54114466	16q12.2	16q12.2		610966	"FTO, GDFD, BMIQ14"	Fat mass- and obesity-associated gene	FTO	79068	ENSG00000140718		"Growth retardation, developmental delay, facial dysmorphism, 612938 (3), Autosomal recessive; {Obesity, susceptibility to, BMIQ14}, 612460 (3), Autosomal recessive"	Fto (MGI:1347093)			
chr16	54283299	54286771	16q12.2	16q12.2		612985	"IRX3, IRXB1"	Iroquois homeobox protein 3	IRX3	79191	ENSG00000177508			Irx3 (MGI:1197522)			
chr16	54918862	54929188	16q12.2	16q12.2		615624	CRNDE	"Colorectal neoplasia differentially expressed gene, noncoding"	CRNDE	643911							
chr16	54931198	54934484	16q11.2-q13	16q12.2		606195	"IRX5, HMMS"	Iroquois homeo box protein 5	IRX5	10265	ENSG00000176842		"Hamamy syndrome, 611174 (3), Autosomal recessive"				
chr16	55323759	55330759	16q11.2-q13	16q12.2		606196	"IRX6, IRX7"	Iroquois homeo box protein 6	IRX6	79190	ENSG00000159387			Irx6 (MGI:1927642)			
chr16	55478829	55506690	16q13	16q12.2		120360	"MMP2, CLG4A, MONA"	"Matrix metalloproteinase 2 (gelatinase A, 72kD type IV collagenase)"	MMP2	4313	ENSG00000087245	"near MT1,2"	"Multicentric osteolysis, nodulosis, and arthropathy, 259600 (3), Autosomal recessive"	Mmp2 (MGI:97009)			
chr16	55509000	55586669	16q12.2	16q12.2		612040	"LPCAT1, AYTL1"	Lysophosphatidylcholine acyltransferase 2	LPCAT2	54947	ENSG00000087253			Lpcat2 (MGI:3606214)			
chr16	55655629	55706191	16q12.2	16q12.2		163970	"SLC6A2, NAT1, NET1"	"Solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2, cocaine- and antidepressant-sensitive"	SLC6A2	6530	ENSG00000103546		"Orthostatic intolerance, 604715 (3)"	Slc6a2 (MGI:1270850)			
chr16	55802850	55833162	16q13-q22.1	16q12.2		114835	"CES1, SES1"	Carboxylesterase 1 (monocyte/macrophage serine esterase 1)	CES1	1066	ENSG00000198848		Carboxylesterase 1 deficiency (3)	Ces1d (MGI:2148202)			
chr16	56000000	66600000	16q13-q21			605746	ANMA	Anisomastia		80871			"Anisomastia, 605746 (2)"				
chr16	56000000	70800000	16q13-q22.1			611031	EKD2	Episodic kinesigenic dyskinesia 2		100124415		max lod at D16S503	"Episodic kinesigenic dyskinesia 2, 611031 (2), Autosomal dominant"				
chr16	56191338	56357443	16q13	16q13		139311	"GNAO1, EIEE17, NEDIM"	"Guanine nucleotide-binding protein (G protein), alpha-activating activity"	GNAO1	2775	ENSG00000087258	close to MT1 in mouse	"Epileptic encephalopathy, early infantile, 17, 615473 (3), Autosomal dominant; Neurodevelopmental disorder with involuntary movements, 617493 (3), Autosomal dominant"	Gnao1 (MGI:95775)			
chr16	56361451	56425537	16q21	16q13		603243	"AMFR, GP78"	Autocrine motility factor receptor	AMFR	267	ENSG00000159461			Amfr (MGI:1345634)			
chr16	56429135	56451348	16q12.2	16q13		604978	"NUDT21, CPSF5, CFIM25"	Nudix hydrolase 21	NUDT21	11051	ENSG00000167005			Nudt21 (MGI:1915469)			
chr16	56451479	56477494	16q13	16q13		615857	OGFOD1	2-oxoglutarate- and iron-dependent oxygenase domain-containing protein 1	OGFOD1	55239	ENSG00000087263			Ogfod1 (MGI:2442978)			
chr16	56470402	56520095	16q21	16q13		606151	"BBS2, RP74"	Bardet-Biedl syndrome 2	BBS2	583	ENSG00000125124		"Bardet-Biedl syndrome 2, 615981 (3), Autosomal recessive; Retinitis pigmentosa 74, 616562 (3), Autosomal recessive"	Bbs2 (MGI:2135267)			
chr16	56565048	56568956	Chr.16	16q13		606206	"MT4, MTIV"	Metallothionein 4	MT4	84560	ENSG00000102891						
chr16	56589336	56591087	16q13	16q13		139255	"MT3, GIFB"	Metallothionein 3 (growth inhibitory factor (neurotrophic))	MT3	4504	ENSG00000087250						
chr16	56608532	56609496	16q13	16q13		156360	"MT2A, MT2"	Metallothionein 2A	MT2A	4502	ENSG00000125148	pseudogene MT2P1 on 4cen-q21					
chr16	56617460	56618817	16q13	16q13		156358	MT1L	Metallothionein 1L	MT1L	4500							
chr16	56625672	56627111	16q13	16q13		156351	MT1E	Metallothionein 1E (functional)	MT1E	4493	ENSG00000169715						
chr16	56632621	56633985	16q13	16q13		156357	MT1K	Metallothionein 1K	MT1M	4499							
chr16	56635738	56637085	16q13	16q13		156356	MT1J	Metallothionein 1J	MT1JP	4498							
chr16	56638665	56640086	16q13	16q13		156350	MT1A	Metallothionein 1A (functional)	MT1A	4489	ENSG00000205362	proximal to FRA16B					
chr16	56651898	56653203	16q13	16q13		156349	MT1B	Metallothionein 1B (functional)	MT1B	4490	ENSG00000169688						
chr16	56657942	56659302	16q13	16q13		156352	MT1F	Metallothionein 1F (functional)	MT1F	4494	ENSG00000198417						
chr16	56666734	56668064	16q13	16q13		156353	MT1G	Metallothionein 1G	MT1G	4495	ENSG00000125144						
chr16	56669813	56671128	16q13	16q13		156354	MT1H	Metallothionein 1H	MT1H	4496	ENSG00000205358						
chr16	56676115	56677876	16q13	16q13		156355	MT1I	Metallothionein 1I	MT1IP	644314							
chr16	56682469	56684195	16q13	16q13		156359	MT1X	Metallothionein 1X	MT1X	4501	ENSG00000187193						
chr16	56730104	56844949	16q13	16q13		614351	"NUP93, NIC96, KIAA0095, NPHS12"	"Nucleoporin, 93kD"	NUP93	9688	ENSG00000102900		"Nephrotic syndrome, type 12, 616892 (3), Autosomal recessive"	Nup93 (MGI:1919055)			
chr16	56858517	56858600	16q13	16q13		613395	"MIR138-2, MIRN138-2"	Micro RNA 138-2	MIR138-2	406930							
chr16	56865206	56915849	16q13	16q13		600968	"SLC12A3, NCCT, TSC"	"Solute carrier family 12 (sodium/potassium/chloride transporters), member 3"	SLC12A3	6559	ENSG00000070915		"Gitelman syndrome, 263800 (3), Autosomal recessive"	Slc12a3 (MGI:108114)			
chr16	56932089	56943880	16q12.2-q13	16q13		608070	"HERPUD1, MIF1, HERP, KIAA0025"	"Homocysteine- and endoplasmic reticulum stress-inducible protein, ubiquitin-like domain-containing, 1"	HERPUD1	9709	ENSG00000051108			Herpud1 (MGI:1927406)			
chr16	56961922	56983843	16q21	16q13		118470	"CETP, HDLCQ10"	"Cholesteryl ester transfer protein, plasma"	CETP	1071	ENSG00000087237		"[High density lipoprotein cholesterol level QTL 10], 143470 (3), Autosomal dominant; Hyperalphalipoproteinemia, 143470 (3), Autosomal dominant"				
chr16	56989484	57083523	16q13	16q13		613537	NLRC5	"NLR family, caspase recruitment domain-containing 5"	NLRC5	84166	ENSG00000140853			Nlrc5 (MGI:3612191)			
chr16	57092542	57147965	16q13	16q13		604206	"CPNE2, CPN2"	Copine II	CPNE2	221184	ENSG00000140848			Cpne2 (MGI:2387578)			
chr16	57152465	57186340	16q13	16q13		617766	"FAM192A, NIP30, C16orf94"	"Family with sequence similarity 192, member A"	FAM192A	80011	ENSG00000172775			Fam192a (MGI:1919637)			
chr16	57186136	57240474	16q13	16q13		616585	"RSPRY1, KIAA1972, SEMDFA"	RING finger- and SPRY domain-containing protein 11	RSPRY1	89970	ENSG00000159579		"Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, 616723 (3), Autosomal recessive"	Rspry1 (MGI:1914860)			
chr16	57245125	57253632	16q13	16q13		615407	"ARL2BP, BART"	ADP ribosylation factor-like 2-binding protein	ARL2BP	23568	ENSG00000102931		"Retinitis pigmentosa with or without situs inversus, 615434 (3), Autosomal recessive"	Arl2bp (MGI:1349429)			
chr16	57256096	57284671	16q13	16q13		600340	"PLLP, PMLP, TM4SF11"	Plasma membrane proteolipid (plasmolipin)	PLLP	51090	ENSG00000102934			Pllp (MGI:1915051)			
chr16	57300000	74100000	16q21-q22			616648	OPA8	Optic atrophy 8	OPA8	106783499		max lod at D16S752	"Optic atrophy 8, 616648 (2), Autosomal dominant"				
chr16	57358782	57366189	16q13	16q21		602957	"CCL22, SCYA22"	"Chemokine, C-C motif, ligand 22"	CCL22	6367	ENSG00000102962			Ccl22 (MGI:1306779)			
chr16	57372457	57385047	16q	16q21		601880	"CX3CL1, SCYD1, NTT, NTN"	"Chemokine, C-X3-C motif, ligand 1 (fractalkine; neurotactin)"	CX3CL1	6376	ENSG00000006210			Cx3cl1 (MGI:1097153)			
chr16	57396075	57416062	16q13	16q21		601520	"CCL17, SCYA17, TARC"	"Chemokine, C-C motif, ligand 17"	CCL17	6361	ENSG00000102970			Ccl17 (MGI:1329039)			
chr16	57428168	57447527	16q21	16q21		608943	CIAPIN1	Cytokine-induced apoptosis inhibitor 1 (anamorsin)	CIAPIN1	57019	ENSG00000005194			Ciapin1 (MGI:1922083)			
chr16	57447424	57461274	16q13	16q21		612837	"COQ9, C16orf49, COQ10D5"	"Coq9, S. cerevisiae, homolog of"	COQ9	57017	ENSG00000088682		"Coenzyme Q10 deficiency, primary, 5, 614654 (3), Autosomal recessive"	Coq9 (MGI:1915164)			
chr16	57462638	57472008	16q13-q21	16q21		180663	POLR2C	"Polymerase (RNA) II (DNA directed) polypeptide C, 33kD"	POLR2C	5432	ENSG00000102978			Polr2c (MGI:109299)			
chr16	57471921	57487138	16q13	16q21		608333	DOK4	Docking protein 4	DOK4	55715	ENSG00000125170			Dok4 (MGI:2148865)			
chr16	57529338	57578181	16q21	16q21		616965	"ADGRG5, GPR114"	Adhesion G protein-coupled receptor G5	ADGRG5	221188	ENSG00000159618			Adgrg5 (MGI:2685955)			
chr16	57619534	57665038	16q13	16q21		604110	"ADGRG1, GPR56, TM7XN1, BFPP, BPPR"	Adhesion G protein-coupled receptor G1	ADGRG1	9289	ENSG00000205336		"Polymicrogyria, bilateral frontoparietal, 606854 (3), Autosomal recessive; Polymicrogyria, bilateral perisylvian, 615752 (3)"	Adgrg1 (MGI:1340051)			
chr16	57735601	57757249	16q21	16q21		602703	"KATNB1, LIS6"	"Katanin, p80 subunit, B1"	KATNB1	10300	ENSG00000140854		"Lissencephaly 6, with microcephaly, 616212 (3), Autosomal recessive"	Katnb1 (MGI:1921437)			
chr16	57758216	57863052	16q13-q21	16q21		604535	KIFC3	Kinesin family member C3	KIFC3	3801	ENSG00000140859			Kifc3 (MGI:109202)			
chr16	57882339	57971115	16q13	16q21		600724	"CNGB1, CNCG3L, CNCG2, RP45"	"Cyclic nucleotide gated channel, beta 1"	CNGB1	1258	ENSG00000070729		"Retinitis pigmentosa 45, 613767 (3), Autosomal recessive"				
chr16	57976434	57988115	16q13	16q21		610264	TEPP	Testis-prostate-placenta-expressed protein	TEPP	374739	ENSG00000159648			Tepp (MGI:1920657)			
chr16	57999598	58021622	16q13	16q21		613276	"USB1, C16orf57, PN"	U6 small nuclear RNA biogenesis phosphodiesterase 1	USB1	79650	ENSG00000103005		"Poikiloderma with neutropenia, 604173 (3), Autosomal recessive"	Usb1 (MGI:2142454)			
chr16	58025565	58046900	16q13-q21	16q21		602261	MMP15	Matrix metalloproteinase 15	MMP15	4324	ENSG00000102996			Mmp15 (MGI:109320)			
chr16	58113587	58129424	16q21	16q21		617906	"CFAP20, BUG22, C16orf80, FSAP23"	Cilia- and flagella-associated protein 20	CFAP20	29105	ENSG00000070761			Cfap20 (MGI:107428)			
chr16	58157902	58197919	16p13.3-p13.2	16q21		115442	CSNK2A2	"Casein kinase-2, alpha-prime polypeptide"	CSNK2A2	1459	ENSG00000070770			Csnk2a2 (MGI:88547)			
chr16	58196861	58283835	16q21	16q21		616070	CCDC113	Coiled-coil domain-containing protein 113	CCDC113	29070	ENSG00000103021			Ccdc113 (MGI:3606076)			
chr16	58392393	58406143	16q21	16q21		610610	"GINS3, PSF3"	GINS complex subunit 3	GINS3	64785	ENSG00000181938			Gins3 (MGI:1926083)			
chr16	58463644	58515402	16q21-q22.3	16q21		614463	"NDRG4, SMAP8, KIAA1180"	NMYC downstream-regulated gene 4	NDRG4	65009	ENSG00000103034			Ndrg4 (MGI:2384590)			
chr16	58515478	58521989	16q21	16q21		616424	SETD6	SET domain-containing protein 6	SETD6	79918	ENSG00000103037			Setd6 (MGI:1913333)			
chr16	58519945	58629885	16q21	16q21		604917	"CNOT1, NOT1"	"CCR4-NOT transcription complex, subunit 1"	CNOT1	23019	ENSG00000125107			Cnot1 (MGI:2442402)			
chr16	58665108	58684776	16q21	16q21		614236	"SLC38A7, SNAT7"	"Solute carrier family 38 (amino acid transporter), member 7"	SLC38A7	55238	ENSG00000103042			Slc38a7 (MGI:2679005)			
chr16	58707130	58734356	16q21	16q21		138150	GOT2	"Glutamic-oxaloacetic transaminase-2, mitochondrial (EC 2.6.1.1)"	GOT2	2806	ENSG00000125166	?pseudogenes on 12 and 1		Got2 (MGI:95792)			
chr16	61640397	62036834	16q21-q22.1	16q21		603008	CDH8	Cadherin-8	CDH8	1006	ENSG00000150394			Cdh8 (MGI:107434)			
chr16	64943752	65126111	16q21-q22.1	16q21		600023	"CDH11, CAD11"	"Cadherin-11 (OB-cadherin, osteoblast)"	CDH11	1009	ENSG00000140937			Cdh11 (MGI:99217)			
chr16	66366606	66404785	16q22.1	16q21		601120	CDH5	Cadherin-5	CDH5	1003	ENSG00000179776			Cdh5 (MGI:105057)			
chr16	66427296	66495287	16q21	16q21		612051	"BEAN, SCA31"	"Brain-expressed, associated with NEDD4"	BEAN1	146227	ENSG00000166546		"Spinocerebellar ataxia 31, 117210 (3), Autosomal dominant"	Bean1 (MGI:1929597)			
chr16	66508002	66550411	16q22	16q21		188250	"TK2, MTDPS2, PEOB3"	"Thymidine kinase, mitochondrial"	TK2	7084	ENSG00000166548	mutation identified in 1 PEOB3 family	"Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560 (3), Autosomal recessive; ?Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3, 617069 (3), Autosomal recessive"	Tk2 (MGI:1913266)			
chr16	66552562	66566286	16q23	16q21		616074	"CKLF, HSPC224"	Chemokine-like factor	CKLF	51192	ENSG00000217555			Cklf (MGI:1922708)			
chr16	66566390	66579134	16q22	16q21		607884	"CMTM1, CKLFSF1"	CKLF-like marvel transmembrane domain-containing 1	CMTM1	113540	ENSG00000089505						
chr16	66579447	66588274	16q22	16q21		607885	"CMTM2, CKLFSF2"	CKLF-like marvel transmembrane domain-containing 2	CMTM2	146225	ENSG00000140932			Cmtm2b (MGI:2447311)			
chr16	66598177	66696706	16q22	16q21-q22		607887	"CMTM4, CKLFSF4"	CKLF-like marvel transmembrane domain-containing 4	CMTM4	146223	ENSG00000183723			Cmtm4 (MGI:2142888)			
chr16	66600000	74100000	16q22			606179	ANBC	Aneurysmal bone cysts		114293		t(16:17); ?defect at 17p13	"Aneurysmal bone cysts, 606179 (2)"				
chr16	66600000	74100000	16q22			613055	ATFB8	"Atrial fibrillation, familial, 8"		100306979		associated with rs7193343	"Atrial fibrillation, familial, 8, 613055 (2)"				
chr16	66600000	74100000	16q22			614541	"C16DELq22, DEL16q22"	Chromosome 16q22 deletion syndrome					"Chromosome 16q22 deletion syndrome, 614541 (4), Isolated cases"				
chr16	66600000	70800000	16q22.1			612590	CRCS9	"Colorectal cancer, susceptibility to, 9"		100329169		associated with rs9929218	"{Colorectal cancer, susceptibility to, 9}, 612590 (2)"				
chr16	66600000	74100000	16q22			604901	NAIC	North American Indian childhood cirrhosis					"North American Indian childhood cirrhosis, 604901 (2)"				
chr16	66600000	79200000	16q22.1-q23.1			611571	OTSC4	Otosclerosis 4	OTSC4	286751		between D16S3107 and D16S3097	"{Otosclerosis 4}, 611571 (2), Autosomal dominant"				
chr16	66600000	70800000	16q22.1			600223	SCA4	Spinocerebellar ataxia 4					"Spinocerebellar ataxia 4, 600223 (2), Autosomal dominant"				
chr16	66603995	66613891	16q22	16q22.1		607886	"CMTM3, CKLFSF3"	CKLF-like marvel transmembrane domain-containing 3	CMTM3	123920	ENSG00000140931			Cmtm3 (MGI:2447162)			
chr16	66754409	66801619	16q22.1	16q22.1		617332	"TERB1, CCDC79"	Telomere repeat-binding bouquet formation protein 1	TERB1	283847	ENSG00000249961			Terb1 (MGI:2443187)			
chr16	66802877	66830976	16q22	16q22.1		603385	"NAE1, APPBP1"	NEDD8 activating enzyme E1 subunit 1	NAE1	8883	ENSG00000159593			Nae1 (MGI:2384561)			
chr16	66844378	66854148	16q21-q23	16q22.1		114770	CA7	Carbonic anhydrase VII	CA7	766	ENSG00000168748			Car7 (MGI:103100)			
chr16	66880360	66891100	16q22.1	16q22.1		615499	"PDP2, KIAA1348"	Pyruvate dehydrogenase phosphatase catalytic subunit 2	PDP2	57546	ENSG00000172840			Pdp2 (MGI:1918878)			
chr16	66908121	66918983	16q22.1	16q22.1		603118	CDH16	Cadherin-16	CDH16	1014	ENSG00000166589			Cdh16 (MGI:106671)			
chr16	66921678	66925535	16q22	16q22.1		179503	RRAD	Ras-related associated with diabetes	RRAD	6236	ENSG00000166592			Rrad (MGI:1930943)			
chr16	66932054	66934422	16q22.1	16q22.1		614778	"FAM96B, MIP18"	"Family with sequence similarity 96, member B"	FAM96B	51647	ENSG00000166595			Fam96b (MGI:1915773)			
chr16	66934443	66945095	16q22.1	16q22.1		605278	CES2	Carboxylesterase 2	CES2	8824	ENSG00000172831			Ces2h (MGI:3648740)			
chr16	66961228	66975151	16q21	16q22.1		605279	"CES3, ES31"	Carboxylesterase 3	CES3	23491	ENSG00000172828			"Ces3a,Ces3b (MGI:102773,MGI:3644960)"			
chr16	67029146	67101057	16q22	16q22.1		121360	"CBFB, PEBP2B"	"Core-binding factor, beta subunit"	CBFB	865	ENSG00000067955	inv(16)(p13;q22); fuses to MYH11	"Myeloid leukemia, acute, M4/M4Eo subtype, somatic, 601626 (1)"	Cbfb (MGI:99851)			
chr16	67154184	67159908	16q22	16q22.1		603500	TRADD	TNRF1-associated death domain protein	TRADD	8717	ENSG00000102871			Tradd (MGI:109200)			
chr16	67159987	67164173	16q22.1	16q22.1		609077	"FBXL8, FBL8"	F-box and leucine-rich repeat protein 8	FBXL8	55336	ENSG00000135722			Fbxl8 (MGI:1354697)			
chr16	67163384	67169944	16q21-q22.1	16q22.1		602438	"HSF4, CTM, CTRCT5"	Heat-shock transcription factor 4	HSF4	3299	ENSG00000102878		"Cataract 5, multiple types, 116800 (3), Autosomal dominant"	Hsf4 (MGI:1347058)			
chr16	67170496	67175736	16q21-q23	16q22.1		605235	"NOL3, NOP, MYC, ARC, FCM"	Nucleolar protein 3	NOL3	8996	ENSG00000140939		"Myoclonus, familial cortical, 614937 (3), Autosomal dominant"	Nol3 (MGI:1925938)			
chr16	67184378	67190203	16q22.1	16q22.1		614117	"EXOC3L1, EXOC3L"	Exocyst complex component 3-like 1	EXOC3L1	283849	ENSG00000179044			Exoc3l (MGI:3041195)			
chr16	67192159	67198917	16q22.1	16q22.1		600659	E2F4	"E2F transcription factor 4, p107/p130-binding"	E2F4	1874	ENSG00000205250			E2f4 (MGI:103012)			
chr16	67202320	67202394	16q22.1	16q22.1		613701	"MIR328, MIRN328"	Micro RNA 328	MIR328	442901							
chr16	67199124	67204028	Chr.16	16q22.1		606422	ELMO3	Engulfment and cell motility gene 3	ELMO3	79767	ENSG00000102890			Elmo3 (MGI:2679007)			
chr16	67229388	67247521	16q22	16q22.1		606881	"FHOD1, FHOS"	Formin homology 2 domain-containing 1	FHOD1	29109	ENSG00000135723						
chr16	67247548	67272203	16q22.1	16q22.1		600477	"SLC9A5, NHE5"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 5"	SLC9A5	6553	ENSG00000135740			Slc9a5 (MGI:2685542)			
chr16	67277819	67289499	16q22.1	16q22.1		609526	PLEKHG4	"Pleckstrin homology domain containing, family G (puratrophin 1)"	PLEKHG4	25894	ENSG00000196155			Plekhg4 (MGI:2142544)			
chr16	67389806	67393534	16q22.1	16q22.1		616957	"TPPP3, p20"	"Tubulin polymerization-promoting protein family, member 3"	TPPP3	51673	ENSG00000159713			Tppp3 (MGI:1915221)			
chr16	67431132	67437552	16q22	16q22.1		614232	"HSD11B2, HSD11K, AME"	Hydroxysteroid (11-beta) dehydrogenase 2	HSD11B2	3291	ENSG00000176387		"Apparent mineralocorticoid excess, 218030 (3), Autosomal recessive"	Hsd11b2 (MGI:104720)			
chr16	67438013	67481185	16q22	16q22.1		607028	ATP6V0D1	"ATPase, H=transporting lysosomal, 38kD, V0 subunit D, isoform 1"	ATP6V0D1	9114	ENSG00000159720			Atp6v0d1 (MGI:1201778)			
chr16	67482570	67483812	16q22	16q22.1		602311	"AGRP, ART, AGRT"	"Agouti-related transcript, mouse, homolog of"	AGRP	181	ENSG00000159723		"{Leanness, inherited} (3); {Obesity, late-onset}, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Agrp (MGI:892013)			
chr16	67562406	67639184	16q22.1	16q22.1		604167	"CTCF, MRD21"	CCCTC-binding factor	CTCF	10664	ENSG00000102974		"Mental retardation, autosomal dominant 21, 615502 (3), Autosomal dominant"	Ctcf (MGI:109447)			
chr16	67644939	67657568	16q22.1	16q22.1		610859	"CARMIL2, RLTPR"	Capping protein regulator and myosin 1 linker 2	CARMIL2	146206	ENSG00000159753			Carmil2 (MGI:2685431)			
chr16	67657511	67660831	16q22.1	16q22.1		609377	"ACD, PTOP, PIP1, TINT1"	"Acd, mouse, homolog of"	ACD	65057	ENSG00000102977	mutation has been identified in 1 DKCA7 and 1 DKCB7 family	"?Dyskeratosis congenita, autosomal dominant 6, 616553 (3), Autosomal recessive, Autosomal dominant; ?Dyskeratosis congenita, autosomal recessive 7, 616553 (3), Autosomal recessive, Autosomal dominant"	Acd (MGI:87873)			
chr16	67723065	67806651	16q22.1	16q22.1		614031	"RANBP10, KIAA1464"	Ran-binding protein 10	RANBP10	57610	ENSG00000141084			Ranbp10 (MGI:1921584)			
chr16	67806572	67828067	16q22.1	16q22.1		607720	"TSNAXIP1, TXI1"	Translin-associated factor X-interacting protein 1	TSNAXIP1	55815	ENSG00000102904			Tsnaxip1 (MGI:1919486)			
chr16	67828156	67847457	16q22.1	16q22.1		611510	CENPT	Centromere protein T	CENPT	80152	ENSG00000102901			Cenpt (MGI:2443939)			
chr16	67842309	67844194	16q22.1	16q22.1		609119	"THAP11, RONIN"	THAP domain-containing protein 11	THAP11	57215	ENSG00000168286			Thap11 (MGI:1930964)			
chr16	67873022	67884513	16q22.1	16q22.1		606030	"EDC4, RCD8, GE1, HEDL5"	Enhancer of mRNA decapping 4	EDC4	23644	ENSG00000038358			Edc4 (MGI:2446249)			
chr16	67893271	67929677	16q22.1	16q22.1		177015	PSKH1	Putative serine kinase H1	PSKH1	5681	ENSG00000159792			Pskh1 (MGI:3528383)			
chr16	67929569	67931874	16q22.1	16q22.1		118888	CTRL	Chymotrypsin-like protease	CTRL	1506	ENSG00000141086			Ctrl (MGI:88558)			
chr16	67934503	67936876	16q22.1	16q22.1		176847	"MECL1, LMP10, PSMB10"	Proteosome subunit MECL1	PSMB10	5699	ENSG00000205220	3.1kb from LCAT		Psmb10 (MGI:1096380)			
chr16	67939883	67944111	16q22.1	16q22.1		606967	LCAT	Lecithin-cholesterol acyltransferase	LCAT	3931	ENSG00000213398	very close to HP	"Fish-eye disease, 136120 (3), Autosomal recessive; Norum disease, 245900 (3), Autosomal recessive"	Lcat (MGI:96755)			
chr16	67943473	67968693	16q22.1	16q22.1		604119	"SLC12A4, KCC1"	"Solute carrier family 12 (potassium/chloride transporters), member 4"	SLC12A4	6560	ENSG00000124067			Slc12a4 (MGI:1309465)			
chr16	67975662	67980548	16q22.1	16q22.1		609926	"DPEP3, MBD3"	Dipeptidase 3	DPEP3	64180	ENSG00000141096			Dpep3 (MGI:1919104)			
chr16	67987389	68000643	16q22.1	16q22.1		609925	"DPEP2, MBD2"	Dipeptidase 2	DPEP2	64174	ENSG00000167261			Dpep2 (MGI:2442042)			
chr16	68021273	68023866	16q22.1	16q22.1		607618	"DDX28, MDDX28"	DEAD/H box 28	DDX28	55794	ENSG00000182810			Ddx28 (MGI:1919236)			
chr16	68022943	68079322	16q22.1	16q22.1		609707	"DUS2L, DUS2"	Dihydrouridine synthase 2-like	DUS2	54920	ENSG00000167264			Dus2 (MGI:1913619)			
chr16	68225967	68236232	16q22.1	16q22.1		612960	"ESRP2, RBM35B"	Epithelial splicing regulatory protein 2	ESRP2	80004	ENSG00000103067			Esrp2 (MGI:1924661)			
chr16	68085365	68229258	Chr.16	16q22.1		602698	NFATC3	"Nuclear factor of activated T cells, cytoplasmic, calcineurin-dependent 3"	NFATC3	4775	ENSG00000072736			Nfatc3 (MGI:103296)			
chr16	68245343	68261061	16q22.1	16q22.1		609362	"LYPLA3, LLPL, ACS, LPLA2"	Lysophospholipase 3	PLA2G15	23659	ENSG00000103066			Pla2g15 (MGI:2178076)			
chr16	68264509	68301822	Chr.16	16q22.1		605641	SLC7A6	"Solute carrier family 7 (y+L-type amino acid transporter), member 6"	SLC7A6	9057	ENSG00000103064			Slc7a6 (MGI:2142598)			
chr16	68310950	68360875	16q22.1	16q22.1		610087	"PRMT7, KIAA1933, SBIDDS"	Protein arginine N-methyltransferase 7	PRMT7	54496	ENSG00000132600		"Short stature, brachydactyly, intellectual developmental disability, and seizures, 617157 (3), Autosomal recessive"	Prmt7 (MGI:2384879)			
chr16	68530248	68576071	16q22.1	16q22.1		609451	"ZFP90, NK10, KIAA1954"	"Zinc finger protein 90, mouse, homolog of"	ZFP90	146198	ENSG00000184939			Zfp90 (MGI:104786)			
chr16	68644835	68727572	16q22.1	16q22.1		114021	"CDH3, CDHP, PCAD, HJMD"	Cadherin-3 (P-cadherin)	CDH3	1001	ENSG00000062038	in mouse tightly linked to ECAD	"Ectodermal dysplasia, ectrodactyly, and macular dystrophy, 225280 (3), Autosomal recessive; Hypotrichosis, congenital, with juvenile macular dystrophy, 601553 (3), Autosomal recessive"	Cdh3 (MGI:88356)			
chr16	68737289	68835541	16q22.1	16q22.1		192090	"CDH1, UVO, LCAM, ECAD, BCDS1"	Cadherin-1 (E-cadherin; uvomorulin)	CDH1	999	ENSG00000039068	near LCAT	"Blepharocheilodontic syndrome 1, 119580 (3), Autosomal dominant; {Breast cancer, lobular}, 114480 (3), Autosomal dominant; Endometrial carcinoma, somatic, 608089 (3); Gastric cancer, familial diffuse, with or without cleft lip and/or palate, 137215 (3), Autosomal dominant; Ovarian carcinoma, somatic, 167000 (3); {Prostate cancer, susceptibility to}, 176807 (3), Autosomal dominant"	Cdh1 (MGI:88354)			
chr16	69105563	69118718	16q22.1	16q22.1		602428	HAS3	Hyaluronan synthase 3	HAS3	3038	ENSG00000103044			Has3 (MGI:109599)			
chr16	69118008	69132589	16q22.1	16q22.1		613202	"CHTF8, CTF8"	"Chromosome transmission fidelity factor 8, S. cerevisiae, homolog of"	CHTF8	54921	ENSG00000168802			Chtf8 (MGI:2443370)			
chr16	69132595	69169033	16q22	16q22.1		607456	"UTP4, CIRH1A, TEX292, KIAA1988"	"Utp4, S. cerevisiae, homolog of"	UTP4	84916	ENSG00000141076			Utp4 (MGI:1096573)			
chr16	69187146	69309051	16q22-q23	16q22.1		600027	"SNTB2, SNT2B2, SNTL"	"Syntrophin, beta-2"	SNTB2	6645	ENSG00000168807			Sntb2 (MGI:101771)			
chr16	69311383	69325042	16q22	16q22.1		609982	"VPS4A, VPS4"	"Vacuolar protein sorting 4, yeast, homolog of, A"	VPS4A	27183	ENSG00000132612			Vps4a (MGI:1890520)			
chr16	69328620	69339622	16q22.1	16q22.1		606979	"COG8, DOR1, CDG2H"	Component of oligomeric golgi complex 8	COG8	84342	ENSG00000272617		"Congenital disorder of glycosylation, type IIh, 611182 (3)"	Cog8 (MGI:2142885)			
chr16	69355560	69386003	16q22.1	16q22.1		602027	"TERF2, TRF2"	Telomeric repeat-binding factor-2	TERF2	7014	ENSG00000132604			Terf2 (MGI:1195972)			
chr16	69424594	69466263	16q22.1	16q22.1		611964	"CYB5B, CYPB5M"	"Cytochrome b5, type B (outer mitochondrial membrane)"	CYB5B	80777	ENSG00000103018			Cyb5b (MGI:1913677)			
chr16	69565951	69704665	16q22.1	16q22.1		604708	"NFAT5, KIAA0827, NFATL1, TONEBP"	Nuclear factor of activated T cells 5	NFAT5	10725	ENSG00000102908			Nfat5 (MGI:1859333)			
chr16	69709400	69726667	16q22.1	16q22.1		125860	"NQO1, DIA4, NMOR1"	"NAD(P)H dehydrogenase, quinone 1 (diaphorase-4)"	NQO1	1728	ENSG00000181019		"{Benzene toxicity, susceptibility to} (3); {Breast cancer, poor survival after chemotherapy for} (3); {Leukemia, post-chemotherapy, susceptibility to} (3)"	Nqo1 (MGI:103187)			
chr16	69762283	69941740	16q21	16q22.1		602308	WWP2	WW domain-containing protein 2	WWP2	11060	ENSG00000198373			Wwp2 (MGI:1914144)			
chr16	69933080	69933179	16q22.1	16q22.1		611894	"MIR140, MIRN140"	Micro RNA 140	MIR140	406932							
chr16	69950231	69968477	16q22.1	16q22.1		616571	CLEC18A	"C-type lecting domain family 18, member A"	CLEC18A	348174	ENSG00000157322						
chr16	70113625	70163630	16q22.1	16q22.1		617835	"PDPR, KIAA1990"	Pyruvate dehydrogenase phosphatase regulatory subunit	PDPR	55066	ENSG00000090857			Pdpr (MGI:2442188)			
chr16	70173321	70187146	16q22.1	16q22.1		616573	CLEC18C	"C-type lectin domain family 18, member C"	CLEC18C	283971	ENSG00000157335						
chr16	70250230	70251929	16q22.1	16q22.1		606490	"EXOSC6, MTR3"	Exosome component 6	EXOSC6	118460	ENSG00000223496			Exosc6 (MGI:1919794)			
chr16	70252294	70289508	16q22	16q22.1		601065	"AARS, CMT2N, EIEE29"	Alanyl-tRNA synthetase	AARS	16	ENSG00000090861		"Charcot-Marie-Tooth disease, axonal, type 2N, 613287 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 29, 616339 (3), Autosomal recessive"	Aars (MGI:2384560)			
chr16	70289766	70335212	Chr.16	16q22.1		605812	"DDX19, DBP5"	DEAD/H box 19	DDX19B	11269	ENSG00000157349			Ddx19b (MGI:2148251)			
chr16	70480568	70523553	16q22.1	16q22.1		606976	"COG4, COD1, CDG2J"	Component of oligomeric golgi complex 4	COG4	25839	ENSG00000103051		"Congenital disorder of glycosylation, type IIj, 613489 (3), Autosomal recessive"	Cog4 (MGI:2142808)			
chr16	70523787	70577667	16q22.1	16q22.1		605592	"SF3B3, SF3B130, SAP130"	"Splicing factor 3B, subunit 3"	SF3B3	23450	ENSG00000189091			Sf3b3 (MGI:1289341)			
chr16	70579894	70660681	16q22.1	16q22.1		612081	"IL34, C16orf77"	Interleukin 34	IL34	146433	ENSG00000157368			Il34 (MGI:1923777)			
chr16	70661203	70686050	16q22.1	16q22.1		616951	"MTSS1L, ABBA1"	Metastasis suppressor 1-like protein	MTSS1L	92154	ENSG00000132613			Mtss1l (MGI:3039591)			
chr16	70687438	70801175	16q22.1	16q22.1-q22.2		604632	"VAC14, TAX1BP2, TRX, SNDC"	"Vac14, S. cerevisiae, homolog of"	VAC14	55697	ENSG00000103043		"Striatonigral degeneration, childhood-onset, 617054 (3), Autosomal recessive"	Vac14 (MGI:2157980)			
chr16	70802083	71230721	16q22.2	16q22.2		610812	"HYDIN, HYDIN1, CILD5"	"Hydin, mouse, homolog of"	HYDIN	54768	ENSG00000157423	duplicated copy on 1q21.1	"Ciliary dyskinesia, primary, 5, 608647 (3), Autosomal recessive"	Hydin (MGI:2389007)			
chr16	71282299	71290177	16q22.2	16q22.2		616190	"CMTR2, MTR2, FTSJD1"	CAP methyltransferase 2	CMTR2	55783	ENSG00000180917			Cmtr2 (MGI:2384580)			
chr16	71358712	71390437	16q22.1	16q22.2		114051	CALB2	"Calbindin 2, 29kD (calretinin)"	CALB2	794	ENSG00000172137			Calb2 (MGI:101914)			
chr16	71447596	71462251	16q22	16q22.2		194527	"ZNF23, KOX16"	Zinc finger protein-32 (KOX16)	ZNF23	7571	ENSG00000167377			Zfp612 (MGI:2443465)			
chr16	71474072	71489350	16q22	16q22.2		194525	"ZNF19, KOX12"	Zinc finger protein-19 (KOX12)	ZNF19	7567	ENSG00000157429	"?16q23, 19q13"					
chr16	71566850	71577094	16q22.1-q22.3	16q22.2		613018	TAT	"Tyrosine aminotransferase, soluble"	TAT	6898	ENSG00000198650		"Tyrosinemia, type II, 276600 (3), Autosomal recessive"	Tat (MGI:98487)			
chr16	71626152	71641964	16q22.2	16q22.2		614094	MARVELD3	Marvel domain-containing protein 3	MARVELD3	91862	ENSG00000140832			Marveld3 (MGI:1920858)			
chr16	71644923	71724700	16q22.3	16q22.2		611066	"PHLPPL, PHLPP2"	PH domain and leucine-rich repeat protein phosphatase-like	PHLPP2	23035	ENSG00000040199			Phlpp2 (MGI:2444928)			
chr16	71728999	71809072	16q23	16q22.2		603533	"AP1G1, ADTG, CLAPG1"	"Adaptor-related protein complex 1, gamma 1 subunit (adaptin, gamma)"	AP1G1	164	ENSG00000166747			Ap1g1 (MGI:101919)			
chr16	71845990	71857332	16q22.2	16q22.2		614301	"ATXN1L, BOAT1"	Ataxin 1-like (brother of ataxin 1)	ATXN1L	342371	ENSG00000224470			Atxn1l (MGI:3694797)			
chr16	71894407	71930638	16q22.2	16q22.2		616434	"IST1, KIAA0174"	"Increased sodium tolerance 1, yeast, homolog of"	IST1	9798	ENSG00000182149			Ist1 (MGI:1919205)			
chr16	71929537	72000400	16q22	16q22.2		607895	PKD1L3	Polycystin 1-like 3	PKD1L3	342372	ENSG00000277481			Pkd1l3 (MGI:2664670)			
chr16	72008743	72025416	16q22	16q22.2		126064	"DHODH, URA1, POADS"	Dihydroorotate dehydrogenase	DHODH	1723	ENSG00000102967		"Miller syndrome, 263750 (3), Autosomal recessive"	Dhodh (MGI:1928378)			
chr16	72044260	72094315	16q22.2	16q22.2		617722	"TXNL4B, DLP, DIM2"	Thioredoxin-like 4B	TXNL4B	54957	ENSG00000140830			Txnl4b (MGI:2443724)			
chr16	72054591	72061055	16q22.1	16q22.2		140100	HP	Haptoglobin	HP	3240	ENSG00000257017	just distal to fra16q22.1	"[Anhaptoglobinemia], 614081 (3); [Hypohaptoglobinemia], 614081 (3)"	Hp (MGI:96211)			
chr16	72063225	72077245	16q22.1	16q22.2		140210	HPR	Haptoglobin-related locus	HPR	3250	ENSG00000261701	2.2kb 3' to HP; multiple tandem genes in blacks					
chr16	72093664	72112911	16q21-q22	16q22.2		605584	"DHX38, DDX38, PRP16"	"DEAH (Asp-Glu-Ala-His) box polypeptide 38 (PRP6, S. cerevisiae, homolog of)"	DHX38	9785	ENSG00000140829			Dhx38 (MGI:1927617)			
chr16	72782884	73058634	16q22.3-q23.1	16q22.2-q22.3		104155	"ZFHX3, ATBF1"	Zinc finger homeobox 3	ZFHX3	463	ENSG00000140836		"{Prostate cancer, susceptibility to, somatic}, 176807 (3)"	Zfhx3 (MGI:99948)			
chr16	72800000	79200000	16q22.3-q23.1			608932	KTCN2	Keratoconus 2		450092			"Keratoconus 2, 608932 (2)"				
chr16	73092348	73093773	16q22.3	16q22.3		615613	"HCCAT5, HTA"	Hepatocellular carcinoma-associated transcript 5	HCCAT5	283902							
chr16	74100000	84100000	16q23			612727	BMND13	Bone mineral density quantitative trait locus 13		100294717		associated with rs16945612	"[Bone mineral density QTL 13], 612727 (2)"				
chr16	74100000	84100000	16q23			608462	HSCR8	"Hirschsprung disease, susceptibility to, 8"		404719			"{Hirschsprung disease, susceptibility to, 8}, 608462 (2)"				
chr16	74296774	74306287	16q23-q24	16q23.1		157970	"PSMD7, MOV34"	"Proteasome 25S subunit, non-ATPase, 7 (Moloney leukemia virus-34 proviral integration homolog)"	PSMD7	5713	ENSG00000103035			Psmd7 (MGI:1351511)			
chr16	74408630	74422247	16q22.3	16q23.1		616572	CLEC18B	"C-type lectin domain family 18, member B"	CLEC18B	497190	ENSG00000140839			Clec18a (MGI:2672935)			
chr16	74447426	74607143	16q22-q23	16q23.1		600753	GLG1	Golgi apparatus protein 1	GLG1	2734	ENSG00000090863			Glg1 (MGI:104967)			
chr16	74621395	74666891	16q23.1	16q23.1		614151	"RFWD3, FANCW"	RING finger and WD repeat domains-containing protein 3	RFWD3	55159	ENSG00000168411	mutation identified in 1 FANCW patient	"?Fanconi anemia, complementation group W, 617784 (3), Autosomal recessive"	Rfwd3 (MGI:2384584)			
chr16	74671854	74701147	16q23.1	16q23.1		615153	MLKL	Mixed lineage kinase domain-like protein	MLKL	197259	ENSG00000168404			Mlkl (MGI:1921818)			
chr16	74712954	74774830	16q23	16q23.1		611026	"FA2H, FAAH, FAXDC1, FAH1, SCS7, SPG35"	Fatty acid 2-hydroxylase	FA2H	79152	ENSG00000103089		"Spastic paraplegia 35, autosomal recessive, 612319 (3), Autosomal recessive"	Fa2h (MGI:2443327)			
chr16	74873567	74985145	16q23.1	16q23.1		617418	"WDR59, KIAA1923"	WD repeat-containing protein 59	WDR59	79726	ENSG00000103091			Wdr59 (MGI:2442115)			
chr16	74999016	75110993	16q23.1	16q23.1		612060	"ZNRF1, NIN283"	Zinc finger and ring finger protein 1	ZNRF1	84937	ENSG00000186187			Znrf1 (MGI:2177308)			
chr16	75111859	75116794	Chr.16	16q23.1		607490	LDHD	D-lactate dehydrogenase	LDHD	197257	ENSG00000166816			Ldhd (MGI:106428)			
chr16	75126284	75172233	16q23.1	16q23.1		617230	"ZFP1, ZNF475"	"Zinc finger protein 1, mouse, homolog of"	ZFP1	162239	ENSG00000184517			Zfp1 (MGI:99154)			
chr16	75218985	75224926	16q23.2-q23.3	16q23.1		118890	CTRB1	Chymotrypsinogen B1	CTRB1	1504	ENSG00000168925	HP-7cM-TAT-9cM-CTRB					
chr16	75228186	75268052	16q23.1	16q23.1		602941	"BCAR1, CRKAS, CAS"	Breast cancer antiestrogen resistance 1	BCAR1	9564	ENSG00000050820			Bcar1 (MGI:108091)			
chr16	75293709	75433488	16q22.2-q22.3	16q23.1		608108	"CFDP1, CP27, BCNT"	Craniofacial development protein 1	CFDP1	10428	ENSG00000153774			Cfdp1 (MGI:1344403)			
chr16	75473123	75495429	16q22	16q23.1		605294	"CHST6, MCDC1"	"Carbohydrate sulfotransferase-6 (GlcNAc-6-sulfotransferase, corneal)"	CHST6	4166	ENSG00000183196		"Macular corneal dystrophy, 217800 (3), Autosomal recessive"	Chst5 (MGI:1931825)			
chr16	75528529	75535169	16q22	16q23.1		604817	CHST5	"Carbohydrate sulfotransferase-5 (GlcNAc-6-O-sulfotransferase, intestinal)"	CHST5	23563	ENSG00000135702						
chr16	75538116	75556285	16q23.1	16q23.1		614949	"TMEM231, JBTS20, MKS11"	Transmembrane protein 231	TMEM231	79583	ENSG00000205084		"Joubert syndrome 20, 614970 (3), Autosomal recessive; Meckel syndrome 11, 615397 (3), Autosomal recessive"	Tmem231 (MGI:2685024)			
chr16	75566350	75577880	16q22.3-q24.1	16q23.1		607452	GABARAPL2	GABA-A receptor-associated protein-like protein 2	GABARAPL2	11345	ENSG00000034713			Gabarapl2 (MGI:1890602)			
chr16	75596878	75623322	16q22.2-q22.3	16q23.1		604230	ADAT1	"Adenosine deaminase, tRNA-specific, 1"	ADAT1	23536	ENSG00000065457			Adat1 (MGI:1353631)			
chr16	75627723	75647686	16q22.2-q22.3	16q23.1		601421	"KARS, CMTRIB, DFNB89"	Lysyl-tRNA synthetase	KARS	3735	ENSG00000065427	mutation identified in 1 CMTRIB patient	"?Charcot-Marie-Tooth disease, recessive intermediate, B, 613641 (3), Autosomal recessive; Deafness, autosomal recessive 89, 613916 (3), Autosomal recessive"	Kars (MGI:1934754)			
chr16	75647736	75657441	16q23.1	16q23.1		605061	"TERF2IP, RAP1"	"Telomeric repeat binding factor 2, interacting protein"	TERF2IP	54386	ENSG00000166848			Terf2ip (MGI:1929871)			
chr16	76277216	76563609	16q22	16q23.1		610518	"CNTNAP4, CASPR4, KIAA1763"	Contactin-associated protein-like 4	CNTNAP4	85445	ENSG00000152910			Cntnap4 (MGI:2183572)			
chr16	77190918	77199645	16q23.1	16q23.1		608954	"MON1B, SRG1, KIAA0872"	"Mon1, S. cerevisiae, homolog of, B"	MON1B	22879	ENSG00000103111			Mon1b (MGI:1923231)			
chr16	77282127	77435113	16q23	16q23.1		607512	"ADAMTS18, MMCAT"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 18"	ADAMTS18	170692	ENSG00000140873		"Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458 (3), Autosomal recessive"	Adamts18 (MGI:2442600)			
chr16	78022545	78032105	16q23	16q23.1		613588	"CLEC3A, CLECSF1"	"C-type lectin domain family 3, member A"	CLEC3A	10143	ENSG00000166509			Clec3a (MGI:2685642)			
chr16	78099412	79212666	16q23.3-q24.1	16q23.1-q23.2		605131	"WWOX, FOR, SCAR12, EIEE28"	WW domain-containing oxidoreductase	WWOX	51741	ENSG00000186153		"Epileptic encephalopathy, early infantile, 28, 616211 (3), Autosomal recessive; Esophageal squamous cell carcinoma, somatic, 133239 (3); Spinocerebellar ataxia, autosomal recessive 12, 614322 (3), Autosomal recessive"	Wwox (MGI:1931237)			
chr16	79202623	79601951	16q22-q23	16q23.2		177075	"MAF, CCA4, CTRCT21, AYGRP"	v-Maf avian musculoaponeurotic fibrosarcoma oncogene homolog	MAF	4094	ENSG00000178573		"Ayme-Gripp syndrome, 601088 (3), Autosomal dominant; Cataract 21, multiple types, 610202 (3), Autosomal dominant"	Maf (MGI:96909)			
chr16	79721311	79770531	16q23.2	16q23.2		616264	"MAFTRR, lincMAF4"	"MAF transcriptional regulator FNA, noncoding"	MAFTRR	102467146							
chr16	80540258	80550810	16q23.3	16q23.2		607168	"DYNLRB2, DNCL2B"	"Dynein, light chain, roadblock-type 2"	DYNLRB2	83657	ENSG00000168589			Dynlrb2 (MGI:1922715)			
chr16	81006497	81033106	16q23.2	16q23.2		611509	CENPN	Centromere protein N	CENPN	55839	ENSG00000166451			Cenpn (MGI:1919405)			
chr16	81035852	81047345	16q23.2	16q23.2		614693	"ATMIN, ASCIZ, KIAA0431"	ATM interactor	ATMIN	23300	ENSG00000166454			Atmin (MGI:2682328)			
chr16	81081946	81096374	16q24	16q23.2		238330	"GCSH, NKH"	Glycine cleavage system H protein	GCSH	2653	ENSG00000140905		"Glycine encephalopathy, 605899 (3), Autosomal recessive"	Gcsh (MGI:1915383)			
chr16	81100878	81220369	16q23.2	16q23.2		607894	"PKD1L2, PC1L2, KIAA1879"	Polycystin 1-like 2	PKD1L2	114780	ENSG00000166473			Pkd1l2 (MGI:2664668)			
chr16	81238447	81291141	16q21-q23	16q23.2		605748	"BCO1, BCMO1, BCDO"	Beta-carotene oxygenase 1	BCO1	53630	ENSG00000135697	mutation identified in 1 HCVAD patient	"?Hypercarotenemia and vitamin A deficiency, autosomal dominant, 115300 (3), Autosomal dominant"	Bco1 (MGI:1926923)			
chr16	81314940	81380197	16q24.1	16q23.2		605379	"GAN, GAN1"	Gigaxonin	GAN	8139	ENSG00000261609		"Giant axonal neuropathy-1, 256850 (3), Autosomal recessive"	Gan (MGI:1890619)			
chr16	81445169	81711761	16q24	16q23.2-q23.3		610112	"CMIP, KIAA1694, TCMIP"	C-MAF-inducing protein	CMIP	80790	ENSG00000153815			Cmip (MGI:1921690)			
chr16	81600000	84100000	16q23.3			613836	ADIPQTL5	"Adiponectin, serum level of, quantitative trait locus 5"		100653375		associated with rs3865188	"{Adiponectin, serum level of, QTL5], 613836 (2)"				
chr16	81779257	81962692	16q24.1	16q23.3		600220	"PLCG2, FCAS3, APLAID"	"Phospholipase C, gamma 2"	PLCG2	5336	ENSG00000197943		"Autoinflammation, antibody deficiency, and immune dysregulation syndrome, 614878 (3), Autosomal dominant; Familial cold autoinflammatory syndrome 3, 614468 (3), Autosomal dominant"	Plcg2 (MGI:97616)			
chr16	81997645	82011525	16q23.3	16q23.3		616164	SDR42E1	"Short-chain dehydrogenase/reductase family 42E, member 1"	SDR42E1	93517	ENSG00000184860			Sdr42e1 (MGI:1921282)			
chr16	82035252	82098533	16q24.1-q24.2	16q23.3		109685	"HSD17B2, EDH17B2"	Hydroxysteroid (17-beta) dehydrogenase 2	HSD17B2	3294	ENSG00000086696			Hsd17b2 (MGI:1096386)			
chr16	82148161	82170223	Chr.16	16q23.3		605500	"MPHOSPH6, MPP"	M-phase phosphoprotein 6	MPHOSPH6	10200	ENSG00000135698			Mphosph6 (MGI:1915783)			
chr16	82626793	83796609	16q24.2-q24.3	16q23.3		601364	"CDH13, CDHH"	"Cadherin-13 (H-cadherin, heart)"	CDH13	1012	ENSG00000140945			Cdh13 (MGI:99551)			
chr16	83807902	83813001	16q23.3	16q23.3		604553	HSBP1	Heat-shock factor-binding protein 1	HSBP1	3281	ENSG00000230989			Hsbp1 (MGI:1915446)			
chr16	83899124	83916181	16q24	16q23.3		606761	"MLYCD, MCD"	Malonyl-CoA decarboxylase	MLYCD	23417	ENSG00000103150		"Malonyl-CoA decarboxylase deficiency, 248360 (3), Autosomal recessive"	Mlycd (MGI:1928485)			
chr16	83953221	83966331	16q23.3	16q23.3		607975	"OSGIN1, OKL38"	Oxidative stress-induced growth inhibitor 1	OSGIN1	29948	ENSG00000140961			Osgin1 (MGI:1919089)			
chr16	84009666	84043371	16q23.3	16q23.3		615585	"SLC38A8, FVH2"	"Solute carrier family 38 (amino acid transporter), member 8"	SLC38A8	146167	ENSG00000166558		"Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3), Autosomal recessive"	Slc38a8 (MGI:2685433)			
chr16	84053760	84116942	16q24	16q23.3-q24.1		603355	"MBTPS1, S1P"	"Membrane-bound transcription factor protease, site 1"	MBTPS1	8720	ENSG00000140943			Mbtps1 (MGI:1927235)			
chr16	84100000	87000000	16q24.1			607687	HDLC3	"High density lipoprotein cholesterol, low serum, 3"		353125			"{High density lipoprotein cholesterol, low serum, 3}, 607687 (2)"				
chr16	84100000	90338345	16q24			613547	STQTL22	Stature quantitative trait locus 22		100529227		linked to rs299956 and rs2076962	"{Stature QTL 22}, 613547 (2)"				
chr16	84145259	84178760	16q24.1	16q24.1		613190	"DNAAF1, LRRC50, ODA7, CILD13"	"Dynein, axonemal, assembly factor 1"	DNAAF1	123872	ENSG00000154099		"Ciliary dyskinesia, primary, 13, 613193 (3), Autosomal recessive"	Dnaaf1 (MGI:1915520)			
chr16	84177846	84187069	16q24	16q24.1		604905	"TAF1C, TAFI110, SL1"	TATA box-binding protein-associated factor 1C	TAF1C	9013	ENSG00000103168			Taf1c (MGI:109576)			
chr16	84221134	84239749	16q24.1	16q24.1		607603	"KCNG4, KV6.3, KV6.4"	"Potassium channel, voltage-gated, subfamily G, member 4"	KCNG4	93107	ENSG00000168418			Kcng4 (MGI:1913983)			
chr16	84292232	84329850	16q24.3	16q24.1		605322	"WFDC1, PS20"	"WAP four-disulfide core domain-1, mouse, homolog of"	WFDC1	58189	ENSG00000103175			Wfdc1 (MGI:1915116)			
chr16	84368522	84465776	16q24.1	16q24.1		613082	"ATP2C2, SPCA2, KIAA0703"	"ATPase, Ca(2+)-transporting, type 2C, member 2"	ATP2C2	9914	ENSG00000064270			Atp2c2 (MGI:1916297)			
chr16	84565595	84618095	16q24.1	16q24.1		606748	"COTL1, CLP"	Coactosin-like protein 1	COTL1	23406	ENSG00000103187	"pseudogenes on 15, 17, and Y"		Cotl1 (MGI:1919292)			
chr16	84699948	84779921	16q24.1	16q24.1		609818	"USP10, KIAA0190"	Ubiquitin-specific protein 10	USP10	9100	ENSG00000103194			Usp10 (MGI:894652)			
chr16	84819980	84909509	16q24.1	16q24.1		612434	CRISPLD2	"Cysteine-rich secretory protein, LCCL domain-containing, 2"	CRISPLD2	83716	ENSG00000103196			Crispld2 (MGI:1926142)			
chr16	84974459	85011534	16q24.1	16q24.1		614604	"ZDHHC7, DHHC7"	Zinc finger DHHC domain-containing protein 7	ZDHHC7	55625	ENSG00000153786			Zdhhc7 (MGI:2142662)			
chr16	85027708	85094229	16q24.1	16q24.1		611675	KIAA0513	KIAA0513 gene	KIAA0513	9764	ENSG00000135709			6430548M08Rik (MGI:2443793)			
chr16	85098351	85112507	16q24.1	16q24.1		617274	FAM92B	"Family with sequence similarity 92, member B"	FAM92B	339145	ENSG00000153789			Fam92b (MGI:3588213)			
chr16	85169511	85676205	16q24.1	16q24.1		616886	"GSE1, KIAA0182"	GSE1 coiled-coil protein	GSE1	23199	ENSG00000131149			Gse1 (MGI:1098275)			
chr16	85677673	85688981	16q24.1	16q24.1		610609	"GINS2, PSF2"	GINS complex subunit 2	GINS2	51659	ENSG00000131153			Gins2 (MGI:1921019)			
chr16	85778623	85799554	16q24.1	16q24.1		604886	"EMC8, NOC4"	ER membrane protein complex subunit 8	EMC8	10328	ENSG00000131148			Emc8 (MGI:1343095)			
chr16	85799566	85807002	16q22-qter	16q24.1		123864	"COX4I1, COX4"	"Cytochrome c oxidase, subunit IV, isoform 1"	COX4I1	1327	ENSG00000131143			Cox4i1 (MGI:88473)			
chr16	85899167	85922605	16q24.1	16q24.1		601565	"IRF8, ICSBP1, IMD32A, IMD32B"	Interferon regulatory factor 8	IRF8	3394	ENSG00000140968		"Immunodeficiency 32A, mycobacteriosis, autosomal dominant, 614893 (3), Autosomal dominant; Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, 614894 (3), Autosomal recessive"	Irf8 (MGI:96395)			
chr16	86196180	86199719	16q24.1	16q24.1		614978	TCONS00024492	Long noncoding RNA TCONS_00024492	LINC01082	100506542							
chr16	86225579	86286246	16q24.1	16q24.1		614977	"LINC01081, TCONS00024764"	Long intergenic non-protein coding RNA 1081	LINC01081	101154687							
chr16	86474524	86508859	16q24.1	16q24.1		614975	"FENDRR, FOXF1AS1, TCONS_00024240"	FOXF1 adjacent noncoding developmental regulatory RNA	FENDRR	400550		partial overlap with FOXF1 promoter					
chr16	86510526	86514463	16q24	16q24.1		601089	"FOXF1, FKHL5, ACDMPV"	Forkhead box F1	FOXF1	2294	ENSG00000103241		"Alveolar capillary dysplasia with misalignment of pulmonary veins, 265380 (3), Autosomal dominant"	Foxf1 (MGI:1347470)			
chr16	86530175	86555839	16q24.1	16q24.1		616820	MTHFSD	Methenyltetrahydrofolate synthetase domain-containing protein	MTHFSD	64779	ENSG00000103248			Mthfsd (MGI:2679252)			
chr16	86567250	86568932	16q24.3	16q24.1		602402	"FOXC2, FKHL14, MFH1"	Forkhead box C2	FOXC2	2303	ENSG00000176692		"Lymphedema-distichiasis syndrome, 153400 (3), Autosomal dominant; Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400 (3), Autosomal dominant"	Foxc2 (MGI:1347481)			
chr16	86578508	86581697	16q24.1	16q24.1		603252	"FOXL1, FKHL11, FREAC7, FKH6"	Forkhead box L1	FOXL1	2300	ENSG00000176678			Foxl1 (MGI:1347469)			
chr16	87326986	87392106	16q24.3	16q24.2		609102	"FBXO31, FBX31, FBXO14, FBX14, MRT45"	F-box only protein 31	FBXO31	79791	ENSG00000103264	mutation identified in 1 MRT45 family	"?Mental retardation, autosomal recessive 45, 615979 (3), Autosomal recessive"	Fbxo31 (MGI:1354708)			
chr16	87392194	87404773	16q24.2	16q24.2		609604	"MAP1LC3B, LC3B"	"Microtubule-associated protein 1, light chain 3, beta"	MAP1LC3B	81631	ENSG00000140941			Map1lc3b (MGI:1914693)			
chr16	87601834	87698155	16q24.3	16q24.2		605268	"JPH3, JP3, HDL2"	Junctophilin 3	JPH3	57338	ENSG00000154118	mutation identified in 1 HDL2 family	"?Huntington disease-like 2, 606438 (3), Autosomal dominant"	Jph3 (MGI:1891497)			
chr16	87830015	87869498	16q24.3	16q24.2		600182	"SLC7A5, D16S469E, MPE16"	"Solute carrier family 7, member 5"	SLC7A5	8140	ENSG00000103257			Slc7a5 (MGI:1298205)			
chr16	87888012	87936574	16q24.3	16q24.2		114761	"CA5A, CA5AD"	Carbonic anhydrase VA (mitochondrial)	CA5A	763	ENSG00000174990	pseudogene on 16p	"Hyperammonemia due to carbonic anhydrase VA deficiency, 615751 (3), Autosomal recessive"	Car5a (MGI:101946)			
chr16	87949215	88077317	16q24	16q24.2		611564	"BANP, SMAR1"	BTG3-associated nuclear protein	BANP	54971	ENSG00000172530			Banp (MGI:1889023)			
chr16	88424804	88440756	16q24	16q24.2		612078	"ZNF469, KIAA1858, BCS1"	Zinc finger protein 469	ZNF469	84627	ENSG00000225614		"Brittle cornea syndrome 1, 229200 (3), Autosomal recessive"	Zfp469 (MGI:2684868)			
chr16	88451781	88535165	16q24.3	16q24.2		601950	"ZFPM1, FOG, FOG1"	"Zinc finger protein, multitype 1 (friend of GATA1)"	ZFPM1	161882	ENSG00000179588			Zfpm1 (MGI:1095400)			
chr16	88638592	88640473	16q24	16q24.2		604628	IL17C	Interleukin 17C	IL17C	27189	ENSG00000124391			Il17c (MGI:2446486)			
chr16	88643288	88651083	16q24	16q24.2		608508	CYBA	"Cytochrome b-245, alpha polypeptide"	CYBA	1535	ENSG00000051523		"Chronic granulomatous disease, autosomal, due to deficiency of CYBA, 233690 (3), Autosomal recessive"	Cyba (MGI:1316658)			
chr16	88651934	88663152	16q24.3	16q24.2		603236	"MVD, MPD, POROK7"	Mevalonate pyrophosphate decarboxylase	MVD	4597	ENSG00000167508		"Porokeratosis 7, multiple types, 614714 (3), Autosomal dominant"	Mvd (MGI:2179327)			
chr16	88677681	88686473	16q24.3	16q24.2		612741	"SNAI3, SNAIL3, SMUC, ZFP293"	"SNAIL, Drosophila, homolog of, 3"	SNAI3	333929	ENSG00000185669			Snai3 (MGI:1353563)			
chr16	88696494	88706420	16q24.2-q24.3	16q24.2-q24.3		617178	RNF166	RING finger protein 166	RNF166	115992	ENSG00000158717			Rnf166 (MGI:1915968)			
chr16	88700000	90338345	16q24.3			612525	IHPS5	"Pyloric stenosis, infantile hypertrophic, 5"		100270639		between rs7197068 and rs750740	"Pyloric stenosis, infantile hypertrophic, 5, 612525 (2)"				
chr16	88715337	88785219	16q24.3	16q24.3		611184	"PIEZO1, FAM38A, MIB, DHS, LMPH3"	PIEZO1 ion channel	PIEZO1	9780	ENSG00000103335		"Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema, 194380 (3), Autosomal dominant; Lymphedema, hereditary, III, 616843 (3), Autosomal recessive"	Piezo1 (MGI:3603204)			
chr16	88803777	88809257	16q24.3	16q24.3		605525	CDT1	Chromatin licensing and DNA replication factor 1	CDT1	81620	ENSG00000167513		"Meier-Gorlin syndrome 4, 613804 (3), Autosomal recessive"	Cdt1 (MGI:1914427)			
chr16	88809468	88811933	16q24.3	16q24.3		102600	"APRT, APRTD"	Adenine phosphoribosyltransferase	APRT	353	ENSG00000198931	"telomeric to GALNS, transcribed in same cen-tel direction"	"Adenine phosphoribosyltransferase deficiency, 614723 (3), Autosomal recessive"	Aprt (MGI:88061)			
chr16	88813733	88856969	16q24.3	16q24.3		612222	"GALNS, MPS4A"	Galactosamine (N-acetyl)-6-sulfate sulfatase	GALNS	2588	ENSG00000141012	centromeric to APRT	"Mucopolysaccharidosis IVA, 253000 (3), Autosomal recessive"	Galns (MGI:1355303)			
chr16	88856219	88862685	16q22.1-q22.2	16q24.3		610970	TRAPPC2L	Trafficking protein particle complex 2-like	TRAPPC2L	51693	ENSG00000167515			Trappc2l (MGI:1916295)			
chr16	88874854	88977148	16q24	16q24.3		603870	"CBFA2T3, MTGR2, MTG16"	"Core-binding factor, alpha subunit 2, translocated to, 3"	CBFA2T3	863	ENSG00000129993			Cbfa2t3 (MGI:1338013)			
chr16	89093808	89160555	16q24.3	16q24.3		614245	ACSF3	Acyl-CoA synthetase family member 3	ACSF3	197322	ENSG00000176715		"Combined malonic and methylmalonic aciduria, 614265 (3)"	Acsf3 (MGI:2182591)			
chr16	89171754	89195491	16q24.3	16q24.3		114019	"CDH15, CDH14, CDH3, MRD3"	"Cadherin-15, M-cadherin (myotubule)"	CDH15	1013	ENSG00000129910	tightly linked to Aprt in mouse	"Mental retardation, autosomal dominant 3, 612580 (3)"	Cdh15 (MGI:106672)			
chr16	89267618	89490560	16q24.3	16q24.3		611192	"ANKRD11, ANCO1, KBGS"	Ankyrin repeat domain-containing protein 11	ANKRD11	29123	ENSG00000167522		"KBG syndrome, 148050 (3), Autosomal dominant"	Ankrd11 (MGI:1924337)			
chr16	89508378	89557767	16q24.3	16q24.3		602783	"PGN, SPG7, CMAR, CAR"	Paraplegin	SPG7	6687	ENSG00000197912		"Spastic paraplegia 7, autosomal recessive, 607259 (3), Autosomal recessive, Autosomal dominant"	Spg7 (MGI:2385906)			
chr16	89560656	89566828	16q24.3	16q24.3		113703	"RPL13, BBC1, D16S44E"	Ribosomal protein L13	RPL13	6137	ENSG00000167526			"Rpl13-ps6,Rpl13 (MGI:3642685,MGI:105922)"			
chr16	89575767	89597245	16q24.3	16q24.3		605689	CPNE7	Copine VII	CPNE7	27132	ENSG00000178773			Cpne7 (MGI:2142747)			
chr16	89613307	89641539	16q24.3	16q24.3		179780	"DPEP1, RDP, MDP, MBD1"	Dipeptidase 1	DPEP1	1800	ENSG00000015413			Dpep1 (MGI:94917)			
chr16	89644430	89657784	16q24.3	16q24.3		164010	"CHMP1A, PCOLN3, PRSM1, PCH8"	"CHMP family, member 1A"	CHMP1A	5119	ENSG00000131165		"Pontocerebellar hypoplasia, type 8, 614961 (3), Autosomal recessive"	Chmp1a (MGI:1920159)			
chr16	89657743	89670457	16q24.3	16q24.3		615409	"SPATA33, C16orf55"	Spermatogenesis-associated protein 33	SPATA33	124045	ENSG00000167523			Spata33 (MGI:2444920)			
chr16	89686611	89696363	16q24	16q24.3		603464	"CDK10, PISSLRE, ALSAS"	Cyclin-dependent kinase 10	CDK10	8558	ENSG00000185324		"Al Kaissi syndrome, 617694 (3), Autosomal recessive"	Cdk10 (MGI:2448549)			
chr16	89720367	89740924	16q24.3	16q24.3		608460	ZFP276	Zinc finger protein 276	ZNF276	92822	ENSG00000158805			Zfp276 (MGI:1888495)			
chr16	89737548	89816657	16q24.3	16q24.3		607139	"FANCA, FACA, FA1, FA, FAA"	"Fanconi anemia, complementation group A"	FANCA	2175	ENSG00000187741	linkage heterogeneity	"Fanconi anemia, complementation group A, 227650 (3), Autosomal recessive"	Fanca (MGI:1341823)			
chr16	89873585	89911383	16q24.3	16q24.3		612326	"TCF25, NULP1, KIAA1049"	Transcription factor 25	TCF25	22980	ENSG00000141002			Tcf25 (MGI:1914105)			
chr16	89917878	89920976	16q24.3	16q24.3		155555	"MC1R, SHEP2, CMM5"	Melanocortin-1 receptor (alpha melanocyte-stimulating hormone receptor)	MC1R	4157	ENSG00000258839		"{Albinism, oculocutaneous, type II, modifier of}, 203200 (3), Autosomal recessive; [Analgesia from kappa-opioid receptor agonist, female-specific], 613098 (3); {Melanoma, cutaneous malignant, 5}, 613099 (3); [Skin/hair/eye pigmentation 2, blond hair/fair skin], 266300 (3), Autosomal recessive; [Skin/hair/eye pigmentation 2, red hair/fair skin], 266300 (3), Autosomal recessive; {UV-induced skin damage}, 266300 (3), Autosomal recessive"	Mc1r (MGI:99456)			
chr16	89922008	89936096	16q24.3	16q24.3		602661	"TUBB3, TUBB4, CFEOM3A, CDCBM1"	"Tubulin, beta-3"	TUBB3	10381	ENSG00000258947		"Cortical dysplasia, complex, with other brain malformations 1, 614039 (3), Autosomal dominant; Fibrosis of extraocular muscles, congenital, 3A, 600638 (3), Autosomal dominant"	Tubb3 (MGI:107813)			
chr16	89972579	90000786	16q24	16q24.3		603020	"AFG3L1, AFG3"	"ATPase family gene 3, yeast, homolog of"	AFG3L1P	172	ENSG00000223959						
chr16	90019628	90044970	16q24.3	16q24.3		605178	"GAS8, GAS11, CILD33"	Growth arrest-specific 8	GAS8	2622	ENSG00000141013		"Ciliary dyskinesia, primary, 33, 616726 (3), Autosomal recessive"	Gas8 (MGI:1202386)			
chr16	90028907	90029900	16q24.3	16q24.3		605179	"GAS8-AS1, C16orf3, EID1"	GAS8 antisense RNA 1	GAS8-AS1	750							
chr16	90039760	90047782	16q24.3	16q24.3		615805	"URAHP, URAH"	"Urate (hydroxyiso-) hydrolase, pseudogene"	URAHP	100130015							
chr16	0	90338345	Chr.16			133290	ESB3	Esterase-B3	ESB3	2097							
chr16	0	90338345	Chr.16			138060	GRLL1	Glucocorticoid receptor-like 1	NR3C1P1	2910							
chr16	0	90338345	Chr.16			147573	IFNR	Interferon production regulator	IFNR	3466							
chr16	0	90338345	Chr.16			247980	LIPB	"Lipase B, lysosomal acid"	LIPB	3989							
chr16	0	90338345	Chr.16			118870	NHCP1	Nonhistone chromosomal protein-1	NHCP1	4805							
chr16	0	90338345	Chr.16			125260	"VDI, DIPI"	Vesicular stomatitis virus defective interfering particle repressor	VDI	7420							
chr17	0	10800000	17p13			608631	ASPG2	"Asperger syndrome, susceptibility to, 2"		431711		breakpoints between CHRNE and GP1BA	"{Asperger syndrome susceptibility 2}, 608631 (2), Isolated cases, Multifactorial"				
chr17	0	3400000	17p13.3			113721	BCPR	Breast cancer-related regulator of TP53					Breast cancer (1)				
chr17	0	25100000	17p			215500	CACD1	"Choroidal dystrophy, central areolar 1"					"Choroidal dystrophy, central areolar 1, 215500 (2), Autosomal recessive"				
chr17	0	10800000	17p13			601202	"CTRCT24, CTAA2"	"Cataract 24, anterior polar"	CTAA2	1484			"Cataract 24, anterior polar, 601202 (2), Autosomal dominant"				
chr17	0	3400000	17p13.3			615674	DDD3	Dowling-Degos disease 3		102997065		max lod at D17S1529	"Dowling-Degos disease 3, 615674 (2), Autosomal dominant"				
chr17	0	3400000	17p13.3			613215	"DUP17p13.3, C17DUPp13.3"	Chromosome 17p13.3 duplication syndrome				includes LIS1 and/or YWHAE	"Chromosome 17p13.3 duplication syndrome, 613215 (4)"				
chr17	0	3400000	17p13.3			247200	"MDLS, MDS, MDCR, DEL17p13.3, C17DELp13.3"	Miller-Dieker lissencephaly syndrome (chromosome 17p13.3 deletion syndrome)					"Miller-Dieker lissencephaly syndrome, 247200 (4), Autosomal dominant"				
chr17	0	16100000	17p13.3-p12			616964	MSPC	"Palmoplantar carcinoma, multiple self-healing"				between rs8065368 and rs2322788	"Palmoplantar carcinoma, multiple self-healing, 616964 (2)"				
chr17	0	10800000	17p13			605779	NDNC7	"Nail disorder, nonsyndromic congenital, 7 (onychodysplasia, isolated congenital)"		81866			"Nail disorder, nonsyndromic congenital, 7, 605779 (2), Autosomal dominant"				
chr17	0	10800000	17p13.3-p13.1			612576	"SHFLD3, DUP17p13.3, C17DUPp13.3"	Split-hand/foot malformation with long bone deficiency 3				max lod at or near D17S1533; contiguous gene duplication syndrome	"Split-hand/foot malformation with long bone deficiency 3, 612576 (4), Autosomal dominant"				
chr17	0	10800000	17p13			613498	SXGQTL1	Sex hormone-binding globulin circulating level quantitative trait locus 1		100528025		associated with rs1799941	"[Sex hormone-binding globulin circulating level QTL 1], 613498 (2)"				
chr17	146804	181629	17p13.3	17p13.3		604568	DOC2B	"Double C2-like domain-containing protein, beta"	DOC2B	8447	ENSG00000272636			Doc2b (MGI:1100497)			
chr17	212148	386266	17p13.3	17p13.3		604881	"RPH3AL, NOC2"	Rabphilin 3A-like	RPH3AL	9501	ENSG00000181031			Rph3al (MGI:1923492)			
chr17	439977	445939	17p13.3	17p13.3		615928	"FAM101B, CFM1"	"Family with sequence similarity 101, member B"	RFLNB	359845	ENSG00000183688			Rflnb (MGI:1923816)			
chr17	508667	714855	17p13.3	17p13.3		615850	"VPS53, HCCS1, PCH2E"	"Vacuolar protein sorting 53, S. cerevisiae, homolog of"	VPS53	55275	ENSG00000141252		"Pontocerebellar hypoplasia, type 2E, 615851 (3), Autosomal recessive"	Vps53 (MGI:1915549)			
chr17	732545	742967	17p13.3	17p13.3		611627	"FAM57A, CT120"	"Family with sequence similarity 57, member A"	FAM57A	79850	ENSG00000167695			Fam57a (MGI:2151840)			
chr17	744420	752867	17p13.3	17p13.3		606969	"GEMIN4, NEDMCR"	"Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities"	GEMIN4	50628	ENSG00000179409		"Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities, 617913 (3), Autosomal recessive"	Gemin4 (MGI:2449313)			
chr17	782328	792508	17p13.3	17p13.3		612600	"RNMTL1, HC90"	RNA methyltransferase-like 1	MRM3	55178	ENSG00000171861			Mrm3 (MGI:1914640)			
chr17	799312	979765	17p13.3	17p13.3		612895	NXN	Nucleoredoxin	NXN	64359	ENSG00000167693			Nxn (MGI:109331)			
chr17	996892	1002182	17p13.3	17p13.3		607251	"TIMM22, TIM22"	"Translocase of inner mitochondrial membrane 22, yeast, homolog of"	TIMM22	29928	ENSG00000177370			Timm22 (MGI:1929742)			
chr17	1003517	1229711	17p13.3	17p13.3		600365	ABR	Active BCR-related gene	ABR	29	ENSG00000159842			Abr (MGI:107771)			
chr17	1270563	1271270	17p13.3	17p13.3		615416	"BHLHA9, BHLHF42, MSSD, CCSPD"	"Basic helix-loop-helix family, member A9"	BHLHA9	727857	ENSG00000205899	mutation identified in 1 CCSPD family	"?Camptosynpolydactyly, complex, 607539 (3), Autosomal recessive; Syndactyly, mesoaxial synostotic, with phalangeal reduction, 609432 (3), Autosomal recessive"	Bhlha9 (MGI:2444198)			
chr17	1279662	1300986	17p13.3	17p13.3		612211	"TUSC5, LOST1"	Tumor suppressor candidate 5	TRARG1	286753	ENSG00000184811			Tusc5 (MGI:3029307)			
chr17	1344538	1400261	17p13.3	17p13.3		605066	"YWHAE, MDCR, MDS"	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform"	YWHAE	7531	ENSG00000108953			Ywhae (MGI:894689)			
chr17	1421352	1456266	17p13.3	17p13.3		164762	CRK	Avian sarcoma virus CT10 (v-crk) oncogene homolog	CRK	1398	ENSG00000167193			Crk (MGI:88508)			
chr17	1464185	1492706	17p13	17p13.3		606538	MYO1C	Myosin IC	MYO1C	4641	ENSG00000197879			Myo1c (MGI:106612)			
chr17	1494574	1516887	17p13.3	17p13.3		607875	"INPP5K, SKIP, MDCCAID"	Inositol polyphosphate-5-phosphatase K	INPP5K	51763	ENSG00000132376		"Muscular dystrophy, congenital, with cataracts and intellectual disability, 617404 (3), Autosomal recessive"	Inpp5k (MGI:1194899)			
chr17	1517988	1562815	17p13.3	17p13.3		600174	"PITPNA, PITPN"	"Phosphotidylinositol transfer protein, alpha"	PITPNA	5306	ENSG00000174238			Pitpna (MGI:99887)			
chr17	1569253	1630013	17p13.3	17p13.3		610791	"SLC43A2, LAT4"	"Solute carrier family 43 (L-type amino acid transporter, member 2"	SLC43A2	124935	ENSG00000167703			Slc43a2 (MGI:2442746)			
chr17	1633857	1645788	17p13.3	17p13.3		607873	"SCARF1, SREC, KIAA0149"	"Scavenger receptor class F, member 1"	SCARF1	8578	ENSG00000074660			Scarf1 (MGI:2449455)			
chr17	1646149	1650097	17p13.3	17p13.3		607848	RILP	RAB-interacting lysosomal protein	RILP	83547	ENSG00000167705			Rilp (MGI:2144271)			
chr17	1650628	1684881	17p13.3	17p13.3		607300	"PRPF8, PRPC8, RP13"	"Precursor mRNA-processing factor 8, S. cerevisiae, homolog of"	PRPF8	10594	ENSG00000174231		"Retinitis pigmentosa 13, 600059 (3), Autosomal dominant"	Prpf8 (MGI:2179381)			
chr17	1713902	1713986	17p13.3	17p13.3		612077	"MIR22, MIRN22"	Micro RNA 22	MIR22	407004							
chr17	1716522	1738598	17p13.3	17p13.3		614218	"WDR81, CAMRQ2"	WD repeat-containing protein 81	WDR81	124997	ENSG00000167716		"Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2, 610185 (3), Autosomal recessive"	Wdr81 (MGI:2681828)			
chr17	1742807	1755264	17pter-p12	17p13.3		613168	"PLI, SERPINF2"	Alpha-2-plasmin inhibitor	SERPINF2	5345	ENSG00000167711		"Alpha-2-plasmin inhibitor deficiency, 262850 (3), Autosomal recessive"	Serpinf2 (MGI:107173)			
chr17	1761924	1777573	17p13.3	17p13.3		172860	"SERPINF1, PEDF, OI6"	"Serpin peptidase inhibitor, clade F, member 1"	SERPINF1	5176	ENSG00000132386	same region as RP13	"Osteogenesis imperfecta, type VI, 613982 (3)"	Serpinf1 (MGI:108080)			
chr17	1829970	1899553	17p13.3	17p13.3		179835	RPA1	"Replication protein A1, 70kD"	RPA1	6117	ENSG00000132383			Rpa1 (MGI:1915525)			
chr17	1934676	2025344	17p13.3	17p13.3		610461	"RTN4RL1, NGRH2, NGR3"	Reticulon 4 receptor-like 1	RTN4RL1	146760	ENSG00000185924			Rtn4rl1 (MGI:2661375)			
chr17	2030111	2043430	17p13.3	17p13.3		603527	"DPH1, DPH2L1, OVCA1, DEDSSH"	"DPH1, S. cerevisiae, homolog of (ovarian cancer gene 1)"	DPH1	1801	ENSG00000108963		"Developmental delay with short stature, dysmorphic features, and sparse hair, 616901 (3), Autosomal recessive"	Dph1 (MGI:2151233)			
chr17	2041982	2043430	17p13.3	17p13.3		607896	OVCA2	Ovarian cancer-associated gene 2	OVCA2	124641	ENSG00000262664			Ovca2 (MGI:2179725)			
chr17	2049907	2050007	17p13.3	17p13.3		610016	"MIR132, MIRN132"	Micro RNA 132	MIR132	406921							
chr17	2050270	2050379	17p13.3	17p13.3		613487	"MIR212, MIRN212"	Micro RNA 212	MIR212	406994							
chr17	2055098	2059686	17p13.3	17p13.3		603825	HIC1	Hypermethylated in cancer	HIC1	3090	ENSG00000177374			Hic1 (MGI:1338010)			
chr17	2059838	2303835	17p13.3	17p13.3		610963	"SMG6, EST1A, KIAA0732"	"SMG6, C. elegans, homolog of"	SMG6	23293	ENSG00000070366			Smg6 (MGI:2144117)			
chr17	2303370	2325266	17p13.3	17p13.3		606477	SRR	Serine racemase	SRR	63826	ENSG00000167720			Srr (MGI:1351636)			
chr17	2322677	2337383	17p13.3	17p13.3		611214	"TSR1, KIAA1401"	"TSR1, 20S r RNA accumulation, S. cerevisiae, homolog of"	TSR1	55720	ENSG00000167721			Tsr1 (MGI:2144566)			
chr17	2336491	2381073	17p13.3	17p13.3		611418	"SGSM2, KIAA0397"	Small G protein signaling modulator 2	SGSM2	9905	ENSG00000141258			Sgsm2 (MGI:2144695)			
chr17	2384059	2400963	17p13.3	17p13.3		603039	"MNT, ROX"	MAX-binding protein	MNT	4335	ENSG00000070444			Mnt (MGI:109150)			
chr17	2593209	2685616	17p13.3	17p13.3		601545	"PAFAH1B1, LIS1"	"Platelet-activating factor acetylhydrolase, isoform 1B, alpha subunit"	PAFAH1B1	5048	ENSG00000007168		"Lissencephaly 1, 607432 (3), Isolated cases; Subcortical laminar heterotopia, 607432 (3), Isolated cases"	Pafah1b1 (MGI:109520)			
chr17	2689385	2711786	17p13.3	17p13.3		616184	"CLUH, CLU1, KIAA0664"	"Clustered mitochondria, D. discoideum, homolog of"	CLUH	23277	ENSG00000132361			Cluh (MGI:1921398)			
chr17	3092057	3092995	17p13.3	17p13.3		164342	"OR1D2, OLFR1"	"Olfactory receptor, family 1, subfamily D, member 2"	OR1D2	4991	ENSG00000184166	cluster of 16 genes in 350kb		Olfr412 (MGI:3030246)			
chr17	3400000	10800000	17p13.2-p13.1			614341	MRT33	"Mental retardation, autosomal recessive 33"		100852394		between rs1367950 and rs1826925	"Mental retardation, autosomal recessive 33, 614341 (2), Autosomal recessive"				
chr17	3440010	3513851	17p13.2	17p13.2		617673	SPATA22	Spermatogenesis-associated protein 22	SPATA22	84690	ENSG00000141255			Spata22 (MGI:2685728)			
chr17	3473645	3502533	17pter-p13	17p13.2		608034	ASPA	Aspartoacylase (aminoacylase-2)	ASPA	443	ENSG00000108381		"Canavan disease, 271900 (3), Autosomal recessive"	Aspa (MGI:87914)			
chr17	3510501	3557994	17p13	17p13.2		607066	"TRPV3, OLMS, FNEPPK2"	"Transient receptor potential cation channel, subfamily V, member 3"	TRPV3	162514	ENSG00000167723	mutation identified in 1 FNEPPK2 family	"Olmsted syndrome, 614594 (3), Autosomal dominant; ?Palmoplantar keratoderma, nonepidermolytic, focal 2, 616400 (3), Autosomal dominant"	Trpv3 (MGI:2181407)			
chr17	3565445	3609410	17p13	17p13.2		602076	"TRPV1, VR1"	"Transient receptor potential cation channel, subfamily V, member 1 (vanilloid receptor 1; capsaicin receptor)"	TRPV1	7442	ENSG00000196689			Trpv1 (MGI:1341787)			
chr17	3608261	3636321	17p13	17p13.2		605060	"SHPK, CARKL"	Sedoheptulokinase	SHPK	23729	ENSG00000197417		"[Sedoheptulokinase deficiency], 617213 (3), Autosomal recessive"	Shpk (MGI:1921887)			
chr17	3636467	3663102	17p13	17p13.2		606272	CTNS	Cystinosin	CTNS	1497	ENSG00000040531	?3 allelic forms	"Cystinosis, atypical nephropathic, 219800 (3), Autosomal recessive; Cystinosis, late-onset juvenile or adolescent nephropathic, 219900 (3), Autosomal recessive; Cystinosis, nephropathic, 219800 (3), Autosomal recessive; Cystinosis, ocular nonnephropathic, 219750 (3), Autosomal recessive"	Ctns (MGI:1932872)			
chr17	3662892	3668678	17p13	17p13.2		616484	"TAX1BP3, TIP1"	TAX1-binding protein 3	TAX1BP3	30851	ENSG00000213977			Tax1bp3 (MGI:1923531)			
chr17	3714624	3803765	17p13	17p13.2		604682	"ITGAE, CD103"	"Integrin, alpha-E"	ITGAE	3682	ENSG00000083457			Itgae (MGI:1298377)			
chr17	3806747	3846250	17p13.2	17p13.2		616624	"NCBP3, C17orf85"	Nuclear cap-binding protein 3	NCBP3	55421	ENSG00000074356			Ncbp3 (MGI:1914124)			
chr17	3896590	3916665	17p13.3	17p13.2		600845	"P2RX1, P2X1"	"Purinergic receptor P2X, ligand-gated ion channel, 1"	P2RX1	5023	ENSG00000108405			P2rx1 (MGI:1098235)			
chr17	3923868	3964463	17p13.3	17p13.2		601929	"ATP2A3, SERCA3"	"ATPase, Ca(2+)-transporting, ubiquitous"	ATP2A3	489	ENSG00000074370			Atp2a3 (MGI:1194503)			
chr17	4163817	4263994	17p13.2	17p13.2		607927	"ANKFY1, ANKHZN, KIAA1255"	Ankyrin repeats- and FYVE domain-containing protein 1	ANKFY1	51479	ENSG00000185722			Ankfy1 (MGI:1337008)			
chr17	4269216	4366673	17p13.2	17p13.2		601569	UBE2G	"Ubiquitin-conjugating enzyme E2G (UBC7, C. elegans, homolog of)"	UBE2G1	7326	ENSG00000132388	possible pseudogene on 1q42		Ube2g1 (MGI:1914378)			
chr17	4433923	4488203	17p13.2	17p13.2		611701	SPNS3	"Spinster, Drosophila, homolog of, 3"	SPNS3	201305	ENSG00000182557			Spns3 (MGI:1924827)			
chr17	4498842	4539036	17p13.2	17p13.2		612584	SPNS2	"Spinster, Drosophila, homolog of, 2"	SPNS2	124976	ENSG00000183018			Spns2 (MGI:2384936)			
chr17	4538895	4555385	17p13.3	17p13.2		604885	"MYBBP1A, P160"	MYB-binding protein 1A	MYBBP1A	10514	ENSG00000132382			Mybbp1a (MGI:106181)			
chr17	4556926	4560919	17p13.2	17p13.2		612341	GGT6	Gamma-glutamyltransferase 6	GGT6	124975	ENSG00000167741			Ggt6 (MGI:1918772)			
chr17	4630918	4641672	17p13.3	17p13.2		152392	ALOX15	Arachidonate 15-lipoxygenase	ALOX15	246	ENSG00000161905			Alox15 (MGI:87997)			
chr17	4671383	4704336	17p13.3	17p13.2		609455	"PELP1, MNAR"	"Proline-, glutamic acid-, and leucine-rich protein 1"	PELP1	27043	ENSG00000141456			Pelp1 (MGI:1922523)			
chr17	4710493	4721499	17p13	17p13.2		107941	ARRB2	"Arrestin, beta 2"	ARRB2	409	ENSG00000141480			Arrb2 (MGI:99474)			
chr17	4731407	4733609	17p13.2	17p13.2		612383	MED11	Mediator complex subunit 11	MED11	400569	ENSG00000161920			Med11 (MGI:1913422)			
chr17	4733528	4739927	17p13	17p13.2		605398	CXCL16	CXC chemokine ligand-16	CXCL16	58191	ENSG00000161921			Cxcl16 (MGI:1932682)			
chr17	4740014	4746118	17p13.2	17p13.2		614312	"ZMYND15, SPGF14"	Zinc finger MYND-containing protein 15	ZMYND15	84225	ENSG00000141497	mutation identified in 1 SPGF14 family	"?Spermatogenic failure 14, 615842 (3), Autosomal recessive"	Zmynd15 (MGI:3603821)			
chr17	4771891	4783210	17p13.3	17p13.2		604657	TM4SF5	"Transmembrane 4 superfamily, member 5"	TM4SF5	9032	ENSG00000142484			Tm4sf5 (MGI:1922854)			
chr17	4796143	4798502	17p13.2	17p13.2		600307	"PSMB6, LMPY"	"Proteasome subunit, beta-type, 6"	PSMB6	5694	ENSG00000142507			Psmb6 (MGI:104880)			
chr17	4807100	4823431	17p13.1	17p13.2		602384	PLD2	Phospholipase D2	PLD2	5338	ENSG00000129219			Pld2 (MGI:892877)			
chr17	4833339	4898060	17p13.1	17p13.2		609426	"MINK1, MINK"	Misshapen/nik-related kinase 1	MINK1	50488	ENSG00000141503			Mink1 (MGI:1355329)			
chr17	4897768	4905018	17p13-p12	17p13.2		100725	"CHRNE, SCCMS, CMS4A, CMS4B, CMS4C"	"Cholinergic receptor, nicotinic, epsilon polypeptide"	CHRNE	1145	ENSG00000108556		"Myasthenic syndrome, congenital, 4A, slow-channel, 605809 (3), Autosomal recessive, Autosomal dominant; Myasthenic syndrome, congenital, 4B, fast-channel, 616324 (3), Autosomal recessive; Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency, 608931 (3), Autosomal recessive"	Chrne (MGI:87894)			
chr17	4932274	4935029	17pter-p12	17p13.2		606672	"GP1BA, BSS, BDPLT1, VWDP, BDPLT3"	"Glycoprotein Ib, platelet, alpha polypeptide"	GP1BA	2811	ENSG00000185245		"Bernard-Soulier syndrome, type A1 (recessive), 231200 (3), Autosomal recessive; Bernard-Soulier syndrome, type A2 (dominant), 153670 (3), Autosomal dominant; {Nonarteritic anterior ischemic optic neuropathy, susceptibility to}, 258660 (3), Autosomal recessive; von Willebrand disease, platelet-type, 177820 (3), Autosomal dominant"	Gp1ba (MGI:1333744)			
chr17	4937129	4940250	17p13.3	17p13.2		604165	"SLC25A11, SLC20A4, OGC"	"Solute carrier family 25 (mitochondrial carrier; oxoglutarate carrier), member 11"	SLC25A11	8402	ENSG00000108528			Slc25a11 (MGI:1915113)			
chr17	4940007	4945222	17p13.2	17p13.2		610431	"RNF167, RING105"	RING finger protein 167	RNF167	26001	ENSG00000108523			Rnf167 (MGI:1917760)			
chr17	4945649	4949087	17p13.3	17p13.2		176610	"PFN1, ALS18"	Profilin-1	PFN1	5216	ENSG00000108518		"Amyotrophic lateral sclerosis 18, 614808 (3)"	Pfn1 (MGI:97549)			
chr17	4949181	4957130	17pter-p12	17p13.2		131370	"ENO3, GSD13"	"Enolase-3, beta, muscle"	ENO3	2027	ENSG00000108515	mutation identified in 1 GSD13 patient	"?Glycogen storage disease XIII, 612932 (3), Autosomal recessive"	Eno3 (MGI:95395)			
chr17	4959225	4967836	17p13.2	17p13.2		610056	SPAG7	Sperm-associated antigen 7	SPAG7	9552	ENSG00000091640			Spag7 (MGI:107380)			
chr17	4967991	4988280	17p13.2	17p13.2		611508	"CAMTA2, KIAA0909"	Calmodulin-binding transcription activator 2	CAMTA2	23125	ENSG00000108509			Camta2 (MGI:2135957)			
chr17	4988129	5006092	17p13	17p13.2		617374	"INCA1, HSD45"	"Inhibitor of CDK, cyclin A1-interacting protein 1"	INCA1	388324	ENSG00000196388			Inca1 (MGI:2144284)			
chr17	4997947	5028398	17p13.2	17p13.2		603060	"KIF1C, LTXS1, KIAA0706, SPAX2"	Kinesin family member 1C	KIF1C	10749	ENSG00000129250		"Spastic ataxia 2, autosomal recessive, 611302 (3), Autosomal recessive"	Kif1c (MGI:1098260)			
chr17	5032601	5035431	17p13.2	17p13.2		607883	"SLC52A1, GPR172B, GPCR42, PAR2, FLJ10060, RBFVD"	"Solute carrier family 52, riboflavin transporter, member 1"	SLC52A1	55065	ENSG00000132517		"Riboflavin deficiency, 615026 (3), Autosomal dominant"				
chr17	5078458	5096373	17pter-p12	17p13.2		194480	ZFP3	Zinc finger protein-3	ZFP3	124961	ENSG00000180787	probably in cluster with ZNF29 proximal to TP53		Zfp3 (MGI:99177)			
chr17	5105733	5123115	17p13.2	17p13.2		616463	"ZNF232, ZSCAN11"	Zinc finger protein 232	ZNF232	7775	ENSG00000167840						
chr17	5116437	5175031	17p13	17p13.2		604334	"USP6, TRE2"	Ubiquitin-specific protease 6	USP6	9098	ENSG00000129204						
chr17	5208919	5234859	17p13.2	17p13.2		614406	"SCIMP, C17orf87"	SLP adaptor- and CSK-interacting membrane protein	SCIMP	388325	ENSG00000161929			Scimp (MGI:3610314)			
chr17	5282262	5386339	17p13	17p13.2		603616	"RABEP1, RABPT5"	RAB GTPase-binding effector protein 1	RABEP1	9135	ENSG00000029725	fused to PDGFRB in CMML		Rabep1 (MGI:1860236)			
chr17	5384832	5419738	17p13	17p13.2		602552	NUP88	"Nucleoporin, 88-kD"	NUP88	4927	ENSG00000108559			Nup88 (MGI:104900)			
chr17	5419640	5433019	17p13	17p13.2		617299	"RPAIN, RIP"	RPA-interacting protein	RPAIN	84268	ENSG00000129197			Rpain (MGI:1916973)			
chr17	5432778	5439150	17p13.3	17p13.2		601269	"C1QBP, HABP1, COXPD33"	Complement component C1q binding protein (hyaluronic acid-binding protein 1)	C1QBP	708	ENSG00000108561		"Combined oxidative phosphorylation deficiency 33, 617713 (3), Autosomal recessive"	C1qbp (MGI:1194505)			
chr17	5440911	5469059	17p13.2	17p13.2		614405	DHX33	DEAH box polypeptide 33	DHX33	56919	ENSG00000005100			Dhx33 (MGI:2445102)			
chr17	5471250	5486229	17p13.2	17p13.2		610304	DERL2	"DER1-like domain family, member 2"	DERL2	51009	ENSG00000072849			Derl2 (MGI:2151483)			
chr17	5486373	5490813	17p13.2	17p13.2		609178	MIS12	"Mis12, S. pombe, homolog of"	MIS12	79003	ENSG00000167842			Mis12 (MGI:1914389)			
chr17	5501398	5584511	17p13	17p13.2		606636	"NLRP1, NALP1, KIAA0926, DEFCAP, CARD7, SLEV1, VAMAS1, MSPC, AIADK"	"NLR family, pyrin domain containing 1"	NLRP1	22861	ENSG00000091592		"Autoinflammation with arthritis and dyskeratosis, 617388 (3), Autosomal recessive, Autosomal dominant; Palmoplantar carcinoma, multiple self-healing, 615225 (3), Autosomal dominant; {Vitiligo-associated multiple autoimmune disease susceptibility 1}, 606579 (3)"	Nlrp1b (MGI:3582959)			
chr17	6423736	6435198	17p13.1	17p13.2		604392	"AIPL1, LCA4"	Arylhydrocarbon-interacting receptor protein-like 1	AIPL1	23746	ENSG00000129221	LCA1 due to GUCY2D mutation also on 17p13.1	"Cone-rod dystrophy, 604393 (3), Autosomal recessive; Leber congenital amaurosis 4, 604393 (3), Autosomal recessive; Retinitis pigmentosa, juvenile, 604393 (3), Autosomal recessive"	Aipl1 (MGI:2148800)			
chr17	6444414	6451064	17p13.2	17p13.2		617611	"PIMREG, RCS1, FAM64A"	PICALM-interacting mitotic regulator	PIMREG	54478	ENSG00000129195			Pimreg (MGI:1924434)			
chr17	6451262	6556556	17p13.1	17p13.2-p13.1		608921	"PITPNM3, NIR1, CORD5"	"Phosphatidylinositol transfer protein, membrane-associated, 3"	PITPNM3	83394	ENSG00000091622		"Cone-rod dystrophy 5, 600977 (3), Autosomal dominant"	Pitpnm3 (MGI:2685726)			
chr17	6500000	10800000	17p13.1			613776	"DEL17p13.1, C17DELp13.1"	Chromosome 17p13.1 deletion syndrome				contiguous gene deletion syndrome	"Chromosome 17p13.1 deletion syndrome, 613776 (4), Autosomal dominant"				
chr17	6578150	6640926	17p13.1	17p13.1		617112	"KIAA0753, OFIP, OFD15"	KIAA0753 gene	KIAA0753	9851	ENSG00000198920	mutation identified in 1 OFD15 patient	"?Orofaciodigital syndrome XV, 617127 (3), Autosomal recessive"	4933427D14Rik (MGI:1921727)			
chr17	6640901	6644540	17p13.1	17p13.1		616967	"TXNDC17, TRP14, TXNL5"	Thioredoxin domain-containing protein 17	TXNDC17	84817	ENSG00000129235			Txndc17 (MGI:1289248)			
chr17	6684712	6713420	17p13-p12	17p13.1		608305	"SLC13A5, NACT, EIEE25"	"Solute carrier family 13 (sodium-dependent citrate transporter), member 5"	SLC13A5	284111	ENSG00000141485		"Epileptic encephalopathy, early infantile, 25, 615905 (3), Autosomal recessive"	Slc13a5 (MGI:3037150)			
chr17	6755407	6775646	17p13.2	17p13.1		606717	XAF1	XIAP-associated factor 1	XAF1	54739	ENSG00000132530			Xaf1 (MGI:3772572)			
chr17	6776232	6787645	17p13.2	17p13.1		609106	"FBXO39, FBX39"	F-box protein 39	FBXO39	162517	ENSG00000177294			Fbxo39 (MGI:3505735)			
chr17	6799980	6831740	17p13.1	17p13.1		609002	TEKT1	Tektin 1	TEKT1	83659	ENSG00000167858			Tekt1 (MGI:1333819)			
chr17	6993790	7010735	17p13.1	17p13.1		152391	ALOX12	Arachidonate 12-lipoxygenase	ALOX12	239	ENSG00000108839	pseudogene also on chr.17		Alox12 (MGI:87998)			
chr17	7012416	7014532	17p13.1	17p13.1		617098	RNASEK	Ribonuclease K	RNASEK	440400	ENSG00000219200			Rnasek (MGI:106369)			
chr17	7014736	7017523	17p13.1	17p13.1		617215	"C17orf49, BAP18"	Chromosome 17 open reading frame 49	C17orf49	124944	ENSG00000258315			0610010K14Rik (MGI:1915609)			
chr17	7017614	7017700	17p13.1	17p13.1		610718	"MIR195, MIRN195"	Micro RNA 195	MIR195	406971							
chr17	7017910	7018021	17p13.1	17p13.1		615672	MIR497	Micro RNA 497	MIR497	574456							
chr17	7023049	7029641	17p13.1	17p13.1		608992	"BCL6B, BAZF"	B-cell lymphoma 6B	BCL6B	255877	ENSG00000161940			Bcl6b (MGI:1278332)			
chr17	7041629	7044410	17p13.2	17p13.1		615765	"SLC16A11, MCT11"	"Solute carrier family 16, member 11"	SLC16A11	162515	ENSG00000174326			Slc16a11 (MGI:2663709)			
chr17	7074536	7080306	17p13.1	17p13.1		605999	"CLEC10A, CLECSF14, MGL, HML, CD301"	"C-type lectin domain family 10, member A"	CLEC10A	10462	ENSG00000132514			"Clec10a,Mgl2 (MGI:2385729,MGI:96975)"			
chr17	7101321	7115537	17p	17p13.1		108361	ASGR2	Asialoglycoprotein receptor-2	ASGR2	433	ENSG00000161944			Asgr2 (MGI:88082)			
chr17	7173430	7179563	17p13-p11	17p13.1		108360	ASGR1	Asialoglycoprotein receptor-1	ASGR1	432	ENSG00000141505			Asgr1 (MGI:88081)			
chr17	7189889	7220049	17p13.1	17p13.1		602887	"DLG4, PSD95, SAP90"	"Discs large, Drosophila, homolog of, 4"	DLG4	1742	ENSG00000132535			Dlg4 (MGI:1277959)			
chr17	7217124	7225266	17p13	17p13.1		609575	"ACADVL, VLCAD"	"Acyl-Coenzyme A dehydrogenase, very long chain"	ACADVL	37	ENSG00000072778		"VLCAD deficiency, 201475 (3), Autosomal recessive"	Acadvl (MGI:895149)			
chr17	7225340	7234543	17p13.1	17p13.1		602151	DVL2	Dishevelled 2	DVL2	1856	ENSG00000004975			Dvl2 (MGI:106613)			
chr17	7235027	7239655	17p13	17p13.1		612910	PHF23	PHD finger protein 23	PHF23	79142	ENSG00000040633			Phf23 (MGI:1925496)			
chr17	7240418	7242433	17p13.1	17p13.1		605125	GABARAP	GABA-A receptor-associated protein	GABARAP	11337	ENSG00000170296			Gabarap (MGI:1861742)			
chr17	7243586	7251939	17p13.1	17p13.1		610684	"CTDNEP1, DULLARD"	C-terminal domain nuclear envelope phosphatase 1	CTDNEP1	23399	ENSG00000175826			Ctdnep1 (MGI:1914431)			
chr17	7251736	7259939	17p13.1	17p13.1		615019	"ELP5, DERP6, C17orf81"	"Elongator acetyltransferase complex, subunit 5"	ELP5	23587	ENSG00000170291			Elp5 (MGI:1859017)			
chr17	7281734	7288047	17p13	17p13.1		138190	"SLC2A4, GLUT4"	"Solute carrier family 2 (facilitated glucose transporter), member 4"	SLC2A4	6517	ENSG00000181856			Slc2a4 (MGI:95758)			
chr17	7288251	7294556	17p13.1	17p13.1		611447	"YBX2, MSY2, CSDA3, DBPC"	Y box-binding protein 2	YBX2	51087	ENSG00000006047			Ybx2 (MGI:1096372)			
chr17	7306998	7312462	17p13-p12	17p13.1		600187	EIF5A	Eukaryotic translation initiation factor-5A	EIF5A	1984	ENSG00000132507			Eif5a (MGI:106248)			
chr17	7312658	7315338	17p13.1	17p13.1		601935	GPS2	G protein pathway suppressor 2	GPS2	2874	ENSG00000132522			Gps2 (MGI:1891751)			
chr17	7315631	7329318	17p13.1	17p13.1		615865	"NEURL4, KIAA1787"	Neuralized E3 ubiquitin protein ligase 4	NEURL4	84461	ENSG00000215041			Neurl4 (MGI:1921092)			
chr17	7351888	7354943	17p13.2	17p13.1		609848	"KCTD11, REn"	Potassium channel tetramerization domain-containing protein 11	KCTD11	147040	ENSG00000213859			Kctd11 (MGI:2448712)			
chr17	7336505	7354943	Chr.17	17p13.1		607763	"CENTB1, KIAA0050, ACAP1"	"Centaurin, beta-1"	ACAP1	9744	ENSG00000072818			Acap1 (MGI:2388270)			
chr17	7354967	7357218	17p13.1	17p13.1		617814	TMEM95	Transmembrane protein 95	TMEM95	339168	ENSG00000182896			Tmem95 (MGI:3779488)			
chr17	7380558	7389963	17p13.1	17p13.1		608076	TNK1	"Tyrosine kinase, nonreceptor, 1"	TNK1	8711	ENSG00000174292			Tnk1 (MGI:1930958)			
chr17	7389726	7394842	17p13.1	17p13.1		607611	PLSCR3	Phospholipid scramblase 3	PLSCR3	57048	ENSG00000187838			Plscr3 (MGI:1917560)			
chr17	7402973	7404137	17p13.1	17p13.1		617779	"TMEM256, C17orf61"	Transmembrane protein 256	TMEM256	254863	ENSG00000205544			Tmem256 (MGI:1916436)			
chr17	7405491	7419863	Chr.17	17p13.1		606479	"NLGN2, KIAA1366"	Neuroligin 2	NLGN2	57555	ENSG00000169992			Nlgn2 (MGI:2681835)			
chr17	7420359	7421631	17p13.1	17p13.1		615116	"SPEM1, C17orf83"	Spermatid maturation protein 1	SPEM1	374768	ENSG00000181323			Spem1 (MGI:1921538)			
chr17	7435442	7437678	17p13.1	17p13.1		613936	"TMEM102, CBAP"	Transmembrane protein 102	TMEM102	284114	ENSG00000181284			Tmem102 (MGI:1921591)			
chr17	7438272	7444931	17q21	17p13.1		601514	"FGF11, FHF3"	Fibroblast growth factor-11	FGF11	2256	ENSG00000161958			Fgf11 (MGI:109167)			
chr17	7445086	7457612	17p12-p11	17p13.1		100710	"CHRNB1, ACHRB, SCCMS, CMS2A, CMS2C"	"Cholinergic receptor, nicotinic, beta polypeptide-1, muscle"	CHRNB1	1140	ENSG00000170175	mutation identified in 1 CMS2C family	"Myasthenic syndrome, congenital, 2A, slow-channel, 616313 (3), Autosomal dominant; ?Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency, 616314 (3), Autosomal recessive"	Chrnb1 (MGI:87890)			
chr17	7459365	7484248	17p13.1	17p13.1		612308	"ZBTB4, KIAA1538"	Zinc finger and BTB domain-containing 4	ZBTB4	57659	ENSG00000174282			Zbtb4 (MGI:1922830)			
chr17	7484378	7514617	17p13.1	17p13.1		180660	"POLR2A, RPOL2"	"Polymerase (RNA) II (DNA directed) polypeptide A, 220kD"	POLR2A	5430				Polr2a (MGI:98086)			
chr17	7549057	7557889	17p13.3	17p13.1		602695	"TNFSF12, TWEAK, APO3L, DR3LG"	"Tumor necrosis factor ligand superfamily, member 12"	TNFSF12	8742	ENSG00000239697			Tnfsf12 (MGI:1196259)			
chr17	7558291	7561607	17p13.1	17p13.1		604472	"TNFSF13, APRIL, TALL2"	"Tumor necrosis factor ligand superfamily, member 13"	TNFSF13	8741	ENSG00000161955			Tnfsf13 (MGI:1916833)			
chr17	7561991	7571968	17p13.1	17p13.1		612844	SENP3	"Sentrin-specific protease family, member 3"	SENP3	26168	ENSG00000161956			Senp3 (MGI:2158736)			
chr17	7572705	7579005	17p13	17p13.1		602641	"EIF4A1, DDX2A"	"Eukaryotic translation initiation factor 4A, isoform 1"	EIF4A1	1973	ENSG00000161960			Eif4a1 (MGI:95303)			
chr17	7579486	7582110	17p13	17p13.1		153634	CD68	Macrophage antigen CD68 (macrosialin)	CD68	968	ENSG00000129226			Cd68 (MGI:88342)			
chr17	7583646	7588211	17p13.1-p12	17p13.1		604041	"MPDU1, SL15, CDGIF"	Mannose-P-dolichol utilization defect 1	MPDU1	9526	ENSG00000129255		"Congenital disorder of glycosylation, type If, 609180 (3), Autosomal recessive"	Mpdu1 (MGI:1346040)			
chr17	7588179	7590169	17p13	17p13.1		601297	"SOX15, SOX20"	SRY (sex-determining region Y)-box 15	SOX15	6665	ENSG00000129194			Sox15 (MGI:98363)			
chr17	7591229	7614896	17p13.1	17p13.1		605339	FXR2	"Fragile X mental retardation, autosomal homolog-2"	FXR2	9513	ENSG00000129245			Fxr2 (MGI:1346074)			
chr17	7614063	7633382	17p13-p12	17p13.1		182205	"SHBG, ABP"	Sex hormone-binding globulin (androgen binding protein)	SHBG	6462	ENSG00000129214			Shbg (MGI:98295)			
chr17	7626233	7627877	17p13.1	17p13.1		611463	"SAT2, SSAT2"	Spermidine/spermine N(1)-acetyltransferase 2	SAT2	112483	ENSG00000141504			Sat2 (MGI:1916465)			
chr17	7646626	7657770	17p	17p13.1		182331	"ATP1B2, AMOG"	"ATPase, Na+K+ transporting, beta-2 polypeptide"	ATP1B2	482	ENSG00000129244			Atp1b2 (MGI:88109)			
chr17	7668401	7687549	17p13.1	17p13.1		191170	"TP53, P53, LFS1 , BCC7"	Tumor protein p53	TP53	7157	ENSG00000141510		"Adrenal cortical carcinoma, 202300 (3), Autosomal recessive; {Basal cell carcinoma 7}, 614740 (3); Breast cancer, 114480 (3), Autosomal dominant; Choroid plexus papilloma, 260500 (3), Autosomal dominant; Colorectal cancer, 114500 (3), Autosomal dominant; {Glioma susceptibility 1}, 137800 (3), Autosomal dominant, Somatic mutation; Hepatocellular carcinoma, 114550 (3), Somatic mutation; Li-Fraumeni syndrome, 151623 (3), Autosomal dominant; Nasopharyngeal carcinoma, 607107 (3); Osteosarcoma, 259500 (3), Autosomal recessive; Pancreatic cancer, 260350 (3), Autosomal dominant, Somatic mutation, Multifactorial"	Trp53 (MGI:98834)			
chr17	7686070	7703501	17p13	17p13.1		612661	"WRAP53, TCAB1, WDR79, DKCB3"	WD repeat-containing protein antisense to TP53	WRAP53	55135	ENSG00000141499		"Dyskeratosis congenita, autosomal recessive 3, 613988 (3), Autosomal recessive"	Wrap53 (MGI:2384933)			
chr17	7705201	7711374	17p13.1-p11.2	17p13.1		602297	"EFNB3, EPLG8, LERK8, EFL6"	Ephrin B3	EFNB3	1949	ENSG00000108947			Efnb3 (MGI:109196)			
chr17	7717353	7833743	17p13	17p13.1		603333	"DNAH2, DNAHC2"	"Dynein, axonemal, heavy chain-2"	DNAH2	146754	ENSG00000183914			Dnah2 (MGI:107731)			
chr17	7834209	7854795	17p13.1	17p13.1		611577	"KDM6B, JMJD3, KIAA0346"	Lysine-specific demethylase 6B	KDM6B	23135	ENSG00000132510			Kdm6b (MGI:2448492)			
chr17	7854885	7856098	17p13.1	17p13.1		617813	TMEM88	Transmembrane protein 88	TMEM88	92162	ENSG00000167874			Tmem88 (MGI:1914270)			
chr17	7884763	7912756	17p13	17p13.1		602120	CHD3	Chromodomain helicase DNA binding protein-3	CHD3	1107	ENSG00000170004			Chd3 (MGI:1344395)			
chr17	7921858	7930345	17p13.1	17p13.1		604111	"KCNAB3, KCNA3B"	"Potassium voltage-gated channel, shaker-related subfamily, beta member 3"	KCNAB3	9196	ENSG00000170049			Kcnab3 (MGI:1336208)			
chr17	7930344	7931998	17p13	17p13.1		610969	"TRAPPC1, MUM2, BET5"	"Trafficking protein particle complex, subunit 1"	TRAPPC1	58485	ENSG00000170043			Trappc1 (MGI:1098727)			
chr17	7932053	7949918	17p13.1	17p13.1		611425	"CNTROB, LIP8"	Centrosomal BRCA2-interacting protein	CNTROB	116840	ENSG00000170037			Cntrob (MGI:2443290)			
chr17	8002669	8020339	17p13.1	17p13.1		600179	"GUCY2D, GUC2D, LCA1, CORD6, RCD2, CACD1"	"Guanylate cyclase 2D, membrane, retina-specific"	GUCY2D	3000	ENSG00000132518	mutation identified in 1 CACD1 family	"?Central areolar choroidal dystrophy 1, 215500 (3), Autosomal recessive; Cone-rod dystrophy 6, 601777 (3), Autosomal dominant; Leber congenital amaurosis 1, 204000 (3), Autosomal recessive"	Gucy2e (MGI:105123)			
chr17	8039039	8049133	17p13.1	17p13.1		603697	ALOX15B	"Arachidonate 15-lipoxygenase, second type"	ALOX15B	247	ENSG00000179593			Alox8 (MGI:1098228)			
chr17	8072635	8087702	17p13.1	17p13.1		603741	"ALOX12B, ARCI2"	"Archidonate 12-lipoxygenase, R type"	ALOX12B	242	ENSG00000179477		"Ichthyosis, congenital, autosomal recessive 2, 242100 (3), Autosomal recessive"	Alox12b (MGI:1274782)			
chr17	8095899	8118915	17p13.1	17p13.1		607206	"ALOXE3, ARCI3"	Arachidonate lipoxygenase 3	ALOXE3	59344	ENSG00000179148		"Ichthyosis, congenital, autosomal recessive 3, 606545 (3), Autosomal recessive"	Aloxe3 (MGI:1345140)			
chr17	8119154	8119226	17p13.1	17p13.1		189918	"TRNAK1, TRK1, TRK-TTT3-4"	Transfer RNA lysine (TTT) 3-4	TRK-TTT3-5	7206							
chr17	8119751	8119822	17p13.1	17p13.1		189919	"TRNAQ1, TRQ1"	tRNA glutamine-1	TRQ-CTG1-5	7228							
chr17	8120313	8120394	17p13.1	17p13.1		189920	"TRNAL2, TRL2"	tRNA leucine-2	TRL-TAG1-1	7208							
chr17	8120589	8126031	17p13.2	17p13.1		608059	"HES7, SCDO4"	"Hairy/enhancer of split, Drosophila, homolog of, 7"	HES7	84667	ENSG00000179111		"Spondylocostal dysostosis 4, autosomal recessive, 613686 (3), Autosomal recessive"	Hes7 (MGI:2135679)			
chr17	8120924	8121011	17p13.1	17p13.1		610406	"TRNAR1, TRR1"	tRNA arginine-1	TRR-TCT2-1	7230							
chr17	8125745	8125815	17p13.1	17p13.1		610407	"TRNAG2, TRG2"	tRNA glycine-2	TRG-GCC2-6	7196		at least 8 copies in this region					
chr17	8140469	8156359	17p12	17p13.1		602260	"PER, RIGUI"	"Period, Drosophila, homolog of"	PER1	5187	ENSG00000179094			Per1 (MGI:1098283)			
chr17	8159146	8162974	17p12	17p13.1		185881	"VAMP2, SYB2"	Vesicle-associated membrane protein-2 (synaptobrevin-2)	VAMP2	6844	ENSG00000220205			Vamp2 (MGI:1313277)			
chr17	8172459	8176410	17p13.1	17p13.1		616183	"TMEM107, MKS13, JBTS29"	Transmembrane protein 107	TMEM107	84314	ENSG00000179029	mutation identified in 1 JBTS29	"?Joubert syndrome 29, 617562 (3), Autosomal recessive; Meckel syndrome 13, 617562 (3), Autosomal recessive; Orofaciodigital syndrome XVI, 617563 (3), Autosomal recessive"	Tmem107 (MGI:1914160)			
chr17	8173452	8173587	17p13.1	17p13.1		616663	"SNORD118, LCC"	"Small nucleolar RNA,  C/D box, 118"	SNORD118	727676			"Leukoencephalopathy, brain calcifications, and cysts, 614561 (3), Autosomal recessive"				
chr17	8188332	8190245	17p13.1	17p13.1		616599	"BORCS6, C17orf59, LYSPERSIN"	"BLOC1-related complex, subunit 6"	BORCS6	54785	ENSG00000196544			Borcs6 (MGI:1919173)			
chr17	8204730	8210766	17p13.1	17p13.1		604970	"STK12, ARK2, AIK2, AIM1"	Serine/threonine protein kinase 12	AURKB	9212	ENSG00000178999			Aurkb (MGI:107168)			
chr17	8224820	8248094	17p13.1	17p13.1		613129	"CTC1, CRMCC, C17orf68, AAF132"	Conserved telomere maintenance component 1	CTC1	80169	ENSG00000178971		"Cerebroretinal microangiopathy with calcifications and cysts, 612199 (3), Autosomal recessive"	Ctc1 (MGI:1916214)			
chr17	8247595	8270490	Chr.17	17p13.1		602133	"PFAS, FGARAT"	phosphoribosylformylglycinamidine synthase (FGAR amidotransferase)	PFAS	5198	ENSG00000178921			Pfas (MGI:2684864)			
chr17	8287762	8295688	17p13.1	17p13.1		610818	SLC25A35	"Solute carrier family 25, member 35"	SLC25A35	399512	ENSG00000125434			Slc25a35 (MGI:1919248)			
chr17	8288496	8290091	17p13.1	17p13.1		607954	"RANGRF, MOG1"	RAN guanine nucleotide release factor	RANGRF	29098	ENSG00000108961			Rangrf (MGI:1889073)			
chr17	8310237	8322515	17p13.1	17p13.1		608504	"ARGEF15, KIAA0915"	Rho guanine nucleotide exchange factor 15	ARHGEF15	22899	ENSG00000198844			Arhgef15 (MGI:3045246)			
chr17	8339839	8346047	17p13.1	17p13.1		610097	"ODF4, OPPO1"	Outer dense fiber of sperm tails 4	ODF4	146852	ENSG00000184650			Odf4 (MGI:2182079)			
chr17	8377515	8383249	17p	17p13.1		603704	"RPL26, DBA11"	Ribosomal protein L26	RPL26	6154	ENSG00000161970	mutation identified in 1 family	"?Diamond-Blackfan anemia 11, 614900 (3), Autosomal dominant"	Rpl26 (MGI:106022)			
chr17	8435851	8472743	Chr.17	17p13.1		607538	NUDEL	Nude-like protein (endooligopeptidase A)	NDEL1	81565	ENSG00000166579			Ndel1 (MGI:1932915)			
chr17	8474204	8631368	17p13	17p13.1		160776	MYH10	"Myosin, heavy polypeptide-10, non-muscle"	MYH10	4628	ENSG00000133026			Myh10 (MGI:1930780)			
chr17	8747531	8759427	17p13.1	17p13.1		617628	SPDYE4	"SPEEDY/RINGO cell cycle regulator family, member E4"	SPDYE4	388333	ENSG00000183318						
chr17	8802722	8870002	17p13.1	17p13.1		611462	"PIK3R6, C17orf38"	"Phosphatidylinositol 3-kinase, regulatory subunit 6"	PIK3R6	146850	ENSG00000276231			Pik3r6 (MGI:2144613)			
chr17	8878915	8965711	17p13.1	17p13.1		611317	"PIK3R5, p101"	"Phosphatidylinositol 3-kinase, regulatory subunit 5"	PIK3R5	23533	ENSG00000141506		"Ataxia-oculomotor apraxia 3, 615217 (3), Autosomal recessive"	Pik3r5 (MGI:2443588)			
chr17	9021541	9243999	17p13.1	17p13.1		601614	"NTN1, NTN1L"	"Netrin 1, mouse, homolog of"	NTN1	9423	ENSG00000065320			Ntn1 (MGI:105088)			
chr17	9250470	9575957	17p12	17p13.1		604203	STX8	Syntaxin 8	STX8	9482	ENSG00000170310			Stx8 (MGI:1890156)			
chr17	9576626	9643458	17p13.1	17p13.1		609804	"WDR16, WDRPUH"	WD repeat-containing protein 16	CFAP52	146845	ENSG00000166596			Cfap52 (MGI:1919110)			
chr17	9771433	9791296	17p13.1	17p13.1		616161	"DHRS7C, SDR32C2"	"Short-chain dehydrogenase reductase family, member 7C"	DHRS7C	201140	ENSG00000184544			Dhrs7c (MGI:1915710)			
chr17	9825507	9894162	17p13.3	17p13.1		603659	GLP2R	Glucagon-like peptide 2 receptor	GLP2R	9340	ENSG00000065325			Glp2r (MGI:2136733)			
chr17	9897709	9905366	17p13.1	17p13.1		179618	RCV1	Recoverin	RCVRN	5957	ENSG00000109047			Rcvrn (MGI:97883)			
chr17	9910608	10198550	17p	17p13.1		603127	GAS7	Growth arrest-specific 7	GAS7	8522	ENSG00000007237			Gas7 (MGI:1202388)			
chr17	10300865	10373004	17p13.1-p12	17p13.1		603487	MYH13	"Myosin, heavy polypeptide 13, skeletal muscle"	MYH13	8735	ENSG00000006788			Myh13 (MGI:1339967)			
chr17	10390324	10421949	17p13.1	17p13.1		160741	"MYH8, DA7"	"Myosin, heavy polypeptide-8, skeletal muscle, perinatal"	MYH8	4626	ENSG00000133020		"Carney complex variant, 608837 (3); Trismus-pseudocamptodactyly syndrome, 158300 (3), Autosomal dominant"	Myh8 (MGI:1339712)			
chr17	10443057	10469558	17p13.1	17p13.1		160742	MYH4	"Myosin, heavy polypeptide-4, skeletal muscle"	MYH4	4622	ENSG00000264424			Myh4 (MGI:1339713)			
chr17	10492306	10518718	17p13.1	17p13.1		160730	MYH1	"Myosin, heavy polypeptide-1, skeletal muscle, adult"	MYH1	4619	ENSG00000109061	cluster = 6 genes in 500kb		Myh1 (MGI:1339711)			
chr17	10521147	10549699	17p13.1	17p13.1		160740	"MYH2, MYPOP"	"Myosin, heavy polypeptide-2, skeletal muscle, adult"	MYH2	4620	ENSG00000125414		"Proximal myopathy and ophthalmoplegia, 605637 (3), Autosomal recessive, Autosomal dominant"	Myh2 (MGI:1339710)			
chr17	10628525	10678346	17p13.1	17p13.1		160720	"MYH3, DA2A, DA2B, DA8"	"Myosin, heavy polypeptide-3, skeletal muscle, embryonic"	MYH3	4621	ENSG00000109063		"Arthrogryposis, distal, type 2A, 193700 (3), Autosomal dominant; Arthrogryposis, distal, type 2B, 601680 (3), Autosomal dominant; Arthrogryposis, distal, type 8, 178110 (3), Autosomal dominant"	Myh3 (MGI:1339709)			
chr17	10672473	10697567	17p13-p12	17p13.1		603644	"SCO1, SCOD1"	SCO1 cytochrome c oxidase assembly protein	SCO1	6341	ENSG00000133028		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Sco1 (MGI:106362)			
chr17	10800000	16100000	17p12			605572	AOMS2	Abdominal obesity-metabolic syndrome QTL2		65077		second QTL on 3q27	"Abdominal obesity-metabolic syndrome, 605572 (2), Autosomal dominant"				
chr17	10800000	33500000	17p12-q11.2			613392	DFNB85	"Deafness, autosomal recessive 85"	DFNB85	100359399		between rs230884 and rs12603885	"Deafness, autosomal recessive 85, 613392 (2), Autosomal recessive"				
chr17	10800000	42800000	17p12-q21.2			614928	ECTD6	"Ectodermal dysplasia 6, hair/nail type"		101101770		between D17S839 and D17S1299	"Ectodermal dysplasia 6, hair/nail type, 614928 (2), Autosomal recessive"				
chr17	10800000	22700000	17p12-p11.2			616652	YUHAL	Yuan-Harel-Lupski syndrome				contiguous gene duplication syndrome	"Yuan-Harel-Lupski syndrome, 616652 (4), Autosomal dominant"				
chr17	10822474	10838100	17p13.1	17p12		612068	PIRT	Phosphoinositide-interacting regulator of transient receptor potential channels	PIRT	644139	ENSG00000233670			Pirt (MGI:2443635)			
chr17	11241422	11564062	17p12	17p12		617327	SHISA6	"Shisa family, member 6"	SHISA6	388336	ENSG00000188803			Shisa6 (MGI:2685725)			
chr17	11598430	11970167	17p12	17p12		603330	"DNAH9, DNAH17L, DNEL1"	"Dynein, axonemal, heavy chain 9"	DNAH9	1770	ENSG00000007174			Dnah9 (MGI:1289279)			
chr17	11957432	12021521	17p13-p12	17p12		194524	"ZNF18, KOX11"	Zinc finger protein-18 (KOX11)	ZNF18	7566	ENSG00000154957			Zkscan6 (MGI:1289293)			
chr17	12020817	12143830	17p11.2	17p12		601335	"SERK1, PRKMK4, MAPKK4, JNKK1"	SAPK/ERK kinase-1	MAP2K4	6416	ENSG00000065559			Map2k4 (MGI:1346869)			
chr17	12665889	12768948	17p11.2	17p12		606127	MYOCD	Myocardin	MYOCD	93649	ENSG00000141052			Myocd (MGI:2137495)			
chr17	12789511	12991643	17p12	17p12		617716	"ARHGAP44, RICH2, KIAA0672"	RHO GTPase-activating protein 44	ARHGAP44	9912	ENSG00000006740			Arhgap44 (MGI:2144423)			
chr17	12991611	13018063	17p11	17p12		605367	"ELAC2, HPC2, COXPD17"	"elaC, E. coli, homolog 2"	ELAC2	60528	ENSG00000006744	at ~365cR	"Combined oxidative phosphorylation deficiency 17, 615440 (3), Autosomal recessive; {Prostate cancer, hereditary, 2, susceptibility to}, 614731 (3)"	Elac2 (MGI:1890496)			
chr17	13494031	13601941	17p12-p11.2	17p12		604057	"HS3ST3A1, 30ST3A1"	Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 3A1	HS3ST3A1	9955	ENSG00000153976			Hs3st3a1 (MGI:1333861)			
chr17	14069401	14208678	17p12-p11.2	17p12		602125	COX10	"Cytochrome c oxidase, subunit X"	COX10	1352	ENSG00000006695		"Leigh syndrome due to mitochondrial COX4 deficiency, 256000 (3), Autosomal recessive, Mitochondrial; Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Cox10 (MGI:1917633)			
chr17	14301049	14349405	17p12-p11.2	17p12		604058	"HS3ST3B1, 30ST3B1"	Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 3B1	HS3ST3B1	9953	ENSG00000125430			Hs3st3b1 (MGI:1333853)			
chr17	15229776	15265372	17p11.2	17p12		601097	"PMP22, CMT1A, CMT1E, DSS, CIDP"	Peripheral myelin protein-22	PMP22	5376	ENSG00000109099	mutation identified in 1 CIDP family	"Charcot-Marie-Tooth disease, type 1A, 118220 (3), Autosomal dominant; Charcot-Marie-Tooth disease, type 1E, 118300 (3), Autosomal dominant; Dejerine-Sottas disease, 145900 (3), Autosomal recessive, Autosomal dominant; ?Neuropathy, inflammatory demyelinating, 139393 (3), ?Autosomal dominant; Neuropathy, recurrent, with pressure palsies, 162500 (3), Autosomal dominant; Roussy-Levy syndrome, 180800 (3), Autosomal dominant"	Pmp22 (MGI:97631)			
chr17	15303810	15343681	17p12	17p12		612683	TEKT3	Tektin 3	TEKT3	64518	ENSG00000125409			Tekt3 (MGI:1918312)			
chr17	15627965	15684310	17p11.2	17p12		609505	"TRIM16, EBBP"	Tripartite motif-containing protein 16	TRIM16	10626	ENSG00000221926			Trim16 (MGI:2137356)			
chr17	15675475	15675642	17p13-p12	17p12		194535	ZNF29	Zinc finger protein-29 (KOX26)	ZNF29P	7577		proximal to TP53					
chr17	15927781	15975895	17p12-p11.2	17p12		600446	ADORA2B	Adenosine A2b receptor	ADORA2B	136	ENSG00000170425	incorrectly put on 10		Adora2b (MGI:99403)			
chr17	15976559	15999691	17p12	17p12		614535	"ZSWIM7, SWS1"	Zinc finger SWIM domain-containing protein 7	ZSWIM7	125150	ENSG00000214941			Zswim7 (MGI:1916997)			
chr17	15999379	16045427	17p12	17p12		613814	"TTC19, MC3DN2"	Tetratricopeptide repeat domain 19	TTC19	54902	ENSG00000011295		"Mitochondrial complex III deficiency, nuclear type 2, 615157 (3), Autosomal recessive"	Ttc19 (MGI:1920045)			
chr17	16030093	16216474	11p11.2	17p12-p11		600849	NCOR1	Nuclear receptor corepressor 1	NCOR1	9611	ENSG00000141027			Ncor1 (MGI:1349717)			
chr17	16100000	25100000	17p11			608904	ADHD2	"Attention deficit-hyperactivity disorder, susceptibility to, 2"		450088			"{Attention deficit-hyperactivity disorder}, 143465 (2), Autosomal dominant"				
chr17	16100000	22700000	17p11.2			607354	"IS2, AIS2"	"Scoliosis, idiopathic 2"		282552		between D17S947 and D17S798	"Scoliosis, idiopathic 2, 607354 (2)"				
chr17	16100000	22700000	17p11.2			610883	PTLS	Potocki-Lupski syndrome				contiguous gene syndrome	"Potocki-Lupski syndrome, 610883 (4), Isolated cases"				
chr17	16100000	22700000	17p11.2-p11.2			604547	VWSM	Van der Woude syndrome modifier		100917							
chr17	16217194	16351799	17p12-p11.2	17p11.2		605947	"PIGL, CHIME"	"Phosphatidylinositol glycan, class L"	PIGL	9487	ENSG00000108474		"CHIME syndrome, 280000 (3), Autosomal recessive"	Pigl (MGI:2681271)			
chr17	16342533	16353497	17p11.2	17p11.2		608139	"CENPV, P30"	Centromere protein V	CENPV	201161	ENSG00000166582			Cenpv (MGI:1920389)			
chr17	16380792	16382744	17p12-p11.1	17p11.2		191339	UBB	Ubiquitin B	UBB	7314	ENSG00000170315		"Cleft palate, isolated, 119540 (2), Autosomal dominant"				
chr17	16415541	16437002	Chr.17	17p11.2		606676	"TRPV2, VRL1"	"Transient receptor potential cation channel, subfamily V, member 2"	TRPV2	51393	ENSG00000187688			Trpv2 (MGI:1341836)			
chr17	16939083	16972087	17p11.2	17p11.2		604907	"TNFRSF13B, TACI, CVID2"	"Tumor necrosis factor receptor superfamily, member 13B"	TNFRSF13B	23495	ENSG00000240505		"Immunodeficiency, common variable, 2, 240500 (3), Autosomal recessive, Autosomal dominant; Immunoglobulin A deficiency 2, 609529 (3)"	Tnfrsf13b (MGI:1889411)			
chr17	17042437	17192647	17p11.2	17p11.2		612935	"MPRIP, MRIP, KIAA0864, RIP3, P116RIP"	Myosin phosphatase Rho-interacting protein	MPRIP	23164	ENSG00000133030			Mprip (MGI:1349438)			
chr17	17200989	17206904	17p11.2	17p11.2		614960	"PLD6, ZUC"	"Phospholipase D family, member 6"	PLD6	201164	ENSG00000179598						
chr17	17206945	17237190	17p11.2	17p11.2		607273	"FLCN, BHD"	Folliculin	FLCN	201163	ENSG00000154803		"Birt-Hogg-Dube syndrome, 135150 (3), Autosomal dominant; Colorectal cancer, somatic, 114500 (3); Pneumothorax, primary spontaneous, 173600 (3), Autosomal dominant; Renal carcinoma, chromophobe, somatic, 144700 (3)"	Flcn (MGI:2442184)			
chr17	17246623	17281302	17p11.2	17p11.2		604665	"COPS3, SGN3"	"COP9 signalosome, subunit 3"	COPS3	8533	ENSG00000141030			Cops3 (MGI:1349409)			
chr17	17303365	17347662	17p11.2	17p11.2		605292	"NT5M, DNT2"	"Deoxyribonucleotidase, mitochondrial (5' nucleotidase, mitochondrial)"	NT5M	56953	ENSG00000205309			Nt5m (MGI:1917127)			
chr17	17476985	17493219	17p11.2	17p11.2		609878	"MED9, MED25, FLJ10193"	"Mediator of RNA polymerase II transcription, subunit 9, S. cerevisiae, homolog of"	MED9	55090	ENSG00000141026			Med9 (MGI:2183151)			
chr17	17494436	17496394	17p11.2	17p11.2		605550	"RASD1, DEXRAS1"	"Ras protein, dexamethasone-induced, 1"	RASD1	51655	ENSG00000108551			Rasd1 (MGI:1270848)			
chr17	17505560	17591986	17p11.2	17p11.2		602391	"PEMT, PEMPT"	Phosphatidylethanolamine N-methyltransferase	PEMT	10400	ENSG00000133027			Pemt (MGI:104535)			
chr17	17681375	17811452	17p11.2	17p11.2		607642	"RAI1, SMCR, SMS"	Retinoic acid-induced gene 1	RAI1	10743	ENSG00000108557		"Smith-Magenis syndrome, 182290 (3), Autosomal dominant, Isolated cases"	Rai1 (MGI:103291)			
chr17	17811348	17837016	17p11.2	17p11.2		184756	SREBF1	Sterol regulatory element binding transcription factor 1	SREBF1	6720	ENSG00000072310			Srebf1 (MGI:107606)			
chr17	17813835	17813930	17p11.2	17p11.2		613486	"MIR33B, MIRN33B"	Micro RNA 33B	MIR33B	693120							
chr17	17843507	17972469	17p11.2	17p11.2		615519	TOM1L2	TOM1-like 2	TOM1L2	146691	ENSG00000175662			Tom1l2 (MGI:2443306)			
chr17	18015058	18039167	17p11.2	17p11.2		608918	"ATPAF2, ATP12, MC5DN1"	"ATP synthase, mitochondrial F1 complex, assembly factor 2"	ATPAF2	91647	ENSG00000171953	mutation identified in 1 MC5DN1 patient	"?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, 604273 (3), Autosomal recessive"	Atpaf2 (MGI:2180561)			
chr17	18039296	18068404	17p11.2	17p11.2		617699	"GID4, VID2, C17orf39"	"GID complex, subunit 4"	GID4	79018	ENSG00000141034			Gid4 (MGI:1914021)			
chr17	18087866	18107984	17p11.2	17p11.2		602986	DRG2	Developmentally regulated GTP-binding protein 2	DRG2	1819	ENSG00000108591			Drg2 (MGI:1342307)			
chr17	18108705	18180243	17p11.2	17p11.2		602666	"MYO15A, DFNB3"	Myosin XVA	MYO15A	51168	ENSG00000091536		"Deafness, autosomal recessive 3, 600316 (3), Autosomal recessive"	Myo15 (MGI:1261811)			
chr17	18183552	18209953	17p11.2	17p11.2		613303	"ALKBH5, ABH5"	"AlkB, E. coli, homolog of, 5"	ALKBH5	54890	ENSG00000091542			Alkbh5 (MGI:2144489)			
chr17	18225592	18244874	17p12-p11.2	17p11.2		600966	"LLGL1, DLG4"	"Lethal giant larvae, Drosophila, homolog of, 1"	LLGL1	3996	ENSG00000131899			Llgl1 (MGI:102682)			
chr17	18244814	18258915	17p11.2	17p11.2		600362	FLII	"Flightless-I, Drosophila, homolog of"	FLII	2314	ENSG00000177731			Flii (MGI:1342286)			
chr17	18260533	18265789	17p11.2	17p11.2		615498	"MEIF2, SMCR7, MID49"	Mitochondrial elongation factor 2	MIEF2	125170	ENSG00000177427			Mief2 (MGI:2144199)			
chr17	18269957	18315091	17p12-p11.2	17p11.2		601243	TOP3A	"Topoisomerase (DNA) III, alpha"	TOP3A	7156	ENSG00000177302			Top3a (MGI:1197527)			
chr17	18315279	18328055	17p11.2	17p11.2		617074	SMCR8	"Smith-Magenis syndrome chromosome region, candidate gene 8"	SMCR8	140775	ENSG00000176994			Smcr8 (MGI:2444720)			
chr17	18327859	18363562	17p11.2	17p11.2		182144	SHMT1	Serine hydroxymethyltransferase (soluble)	SHMT1	6470	ENSG00000176974	?role in Smith-Magenis syndrome		Shmt1 (MGI:98299)			
chr17	18497089	18503284	17p13.1-q25	17p11.2		600719	NOS2B	Nitric oxide synthase 2B	NOS2P2	201288							
chr17	18744012	18779348	17p12	17p11.2		611679	FBXW10	F-box and WD40 domain protein 10	FBXW10	10517	ENSG00000171931			Fbxw10 (MGI:3052463)			
chr17	18856298	18931286	17p12-p11.2	17p11.2		603762	"PRPSAP2, PAP41"	Phosphoribosylpyrophosphate synthetase-associated protein 2	PRPSAP2	5636	ENSG00000141127			Prpsap2 (MGI:2384838)			
chr17	19188015	19188231	17p11.2	17p11.2		180710	RNU3	"RNA, U3 small nuclear"	SNORD3A	780851		deleted in Smith-Magenis syndrome					
chr17	19335371	19378192	17p11.2	17p11.2		614144	"B9D1, MKSR1, MKS9, JBTS27"	B9 domain-containing protein 1	B9D1	27077	ENSG00000108641	mutation identified in 1 MKS9 patient	"Joubert syndrome 27, 617120 (3), Autosomal recessive; ?Meckel syndrome 9, 614209 (3), Autosomal recessive"	B9d1 (MGI:1351471)			
chr17	19237376	19336714	Chr.17	17p11.2		607263	"EPN2, KIAA1065"	Epsin 2	EPN2	22905	ENSG00000072134			Epn2 (MGI:1333766)			
chr17	19377720	19383543	17p11.2	17p11.2		602521	"MAPK7, PRKM7, ERK5"	Mitogen-activated protein kinase 7 (extracellular signal-regulated kinase 5)	MAPK7	5598	ENSG00000166484			Mapk7 (MGI:1346347)			
chr17	19383441	19387218	17p11.2	17p11.2		600596	MFAP4	Microfibrillar-associated protein-4	MFAP4	4239	ENSG00000166482			Mfap4 (MGI:1342276)			
chr17	19406978	19417275	17p11.2	17p11.2		601237	"RNF112, ZNF179, BFP"	RING finger protein 112	RNF112	7732	ENSG00000128482			Rnf112 (MGI:106611)			
chr17	19533853	19579032	17p11.2	17p11.2		609832	"SLC47A1, MATE1, FLJ10847"	"Solute carrier family 47, member 1"	SLC47A1	55244	ENSG00000142494			Slc47a1 (MGI:1914723)			
chr17	19648145	19677595	17p11.2	17p11.2		609523	"ALDH3A2, ALDH10, SLS, FALDH"	"Aldehyde dehydrogenase 3 family, member A2 (fatty aldehyde dehydrogenase)"	ALDH3A2	224	ENSG00000072210		"Sjogren-Larsson syndrome, 270200 (3), Autosomal recessive"	Aldh3a2 (MGI:1353452)			
chr17	19678312	19719597	17p11.2	17p11.2		609833	"SLC47A2, MATE2, FLJ31196, MATE2K"	"Solute carrier family 47, member 2"	SLC47A2	146802	ENSG00000180638						
chr17	19737983	19748432	17p11.2	17p11.2		100660	"ALDH3A1, ALDH3"	"Aldehyde dehydrogenase 3 family, member A1"	ALDH3A1	218	ENSG00000108602			Aldh3a1 (MGI:1353451)			
chr17	19770827	19867925	17p11.2	17p11.2		608650	"ULK2, KIAA0623, UNC51.2"	UNC51-like kinase 2	ULK2	9706	ENSG00000083290			Ulk2 (MGI:1352758)			
chr17	19904301	19977855	17p11.1	17p11.2		604694	AKAP10	A-kinase anchor protein 10	AKAP10	11216	ENSG00000108599		"{Cardiac conduction defect, susceptibility to}, 115080 (3), Autosomal dominant"	Akap10 (MGI:1890218)			
chr17	20009300	20319025	17p11.2	17p11.2		608793	"SPECC1, HCMOGT1, NSP"	Sperm antigen with calponin homology and coiled-coil domains 1	SPECC1	92521	ENSG00000128487			Specc1 (MGI:2442356)			
chr17	20999592	21043408	17p11.2	17p11.2		612116	"USP22, KIAA1064"	Ubiquitin-specific protease 22	USP22	23326	ENSG00000124422			Usp22 (MGI:2144157)			
chr17	21123367	21192029	17p11.2	17p11.2		616160	"DHRS7B, SDR32C1"	"Short-chain dehydrogenase reductase family, member 7B"	DHRS7B	25979	ENSG00000109016			Dhrs7b (MGI:2384931)			
chr17	21284655	21315239	17q11.2	17p11.2		602315	"PRKMK3, MAPKK3, MEK3"	"Protein kinase, mitogen-activated, kinase-3"	MAP2K3	5606	ENSG00000034152			Map2k3 (MGI:1346868)			
chr17	21376386	21419869	17p11.2-p11.1	17p11.2		602323	"KCNJ12, KCNJN1"	"Potassium inwardly-rectifying channel, subfamily J, member 12"	KCNJ12	3768	ENSG00000184185			Kcnj12 (MGI:108495)			
chr17	21692522	21705699	17p11.2	17p11.2		613236	"KCNJ18, KIR2.6, TTPP2"	"Potassium channel, inwardly rectifying, subfamily J, member 18"	KCNJ18	100134444	ENSG00000260458		"{Thyrotoxic periodic paralysis, susceptibility to, 2}, 613239 (3), Isolated cases"				
chr17	22406018	22413740	17p11.2	17p11.2		605160	"PRG4, FLJ36000"	p53-responsive gene 4		284124							
chr17	22523110	22524664	17p11.2	17p11.2		616985	"MTRNR2L1, HN1"	MTRNR2-like 1	MTRNR2L1	100462977	ENSG00000256618						
chr17	25100000	33500000	17q11			609378	AUTS6	"Autism, susceptibility to, 6"		554314		max lod at D17S1800	"{Autism susceptibility 6}, 609378 (2)"				
chr17	25100000	33500000	17q11			606601	"ERVE1, HERVE1"	"Endogenous retroviral sequence E, 1"	ERVE-1	85314							
chr17	25100000	83257441	17q			603918	HYT1	"Hypertension, essential, susceptibility to, 1"		117191		~18cM distal to ACE	"{Hypertension, essential, susceptibility to, 1}, 145500 (2), Multifactorial"				
chr17	27294020	27313630	17q11.1	17q11.1		610091	"WSB1, SWIP1"	WD repeat- and SOCS box-containing protein 1	WSB1	26118	ENSG00000109046			Wsb1 (MGI:1926139)			
chr17	27400000	33500000	17q11.2			601395	"CCL3L1, SCYA3L1, LD78"	"Chemokine, C-C motif, ligand 3-like 1"	CCL3L1	6349	ENSG00000276085	varies in copy number 1-10	"{HIV/AIDS, susceptibility to}, 609423 (3)"				
chr17	27400000	33500000	17q11.2			613675	"DEL17q11.2, C17DELq11.2"	"Chromosome 17q11.2 deletion syndrome, 1.4Mb (NF1 microdeletion syndrome)"					"Chromosome 17q11.2 deletion syndrome, 1.4Mb, 613675 (4), Autosomal dominant"				
chr17	27400000	72900000	17q11.2-q24			154275	MHS2	Malignant hyperthermia susceptibility 2	MHS2	4264		?due to mutation in SCN4A	"{Malignant hyperthermia susceptibility 2}, 154275 (2), Autosomal dominant"				
chr17	27400000	33500000	17q11.2			612575	MPVQTL3	Mean platelet volume quantitative trait locus 3		100271869		associated with rs2138852	"[Mean platelet volume QTL3], 612575 (2)"				
chr17	27456440	27626437	17q11.2	17q11.2		601132	"KSR, KSR1"	Kinase suppressor of RAS	KSR1	8844	ENSG00000141068			Ksr1 (MGI:105051)			
chr17	27631147	27649559	17q11.2	17q11.2		601879	LGALS9	"Lectin, galactoside-binding, soluble, 9"	LGALS9	3965	ENSG00000168961						
chr17	27651442	27664654	17p13.1-q25	17q11.2		600720	NOS2C	Nitric oxide synthase 2C	NOS2P1	645740							
chr17	27756765	27800528	17cen-q11.2	17q11.2		163730	"NOS2A, NOS2"	"Nitric oxide synthase 2A, inducible, hepatocytes"	NOS2	4843	ENSG00000007171	?cluster of 3 NOS2 genes	"{Hypertension, susceptibility to}, 145500 (2), Multifactorial; {Malaria, resistance to}, 611162 (3)"	Nos2 (MGI:97361)			
chr17	28226562	28228059	17q11	17q11.2		606637	PYY2	"Peptide YY, 2"	PYY2	23615							
chr17	28247443	28248288	17q11	17q11.2		606638	PPY2	Pancreatic polypeptide 2	PPY2P	23614							
chr17	28319040	28328684	17q11.2	17q11.2		612912	"TMEM97, MAC30"	Transmembrane protein 97	TMEM97	27346	ENSG00000109084			Tmem97 (MGI:1916321)			
chr17	28328324	28335488	17p11.1	17q11.2		614394	IFT20	"Intraflagellar transport 20, chlamydomonas, homolog of"	IFT20	90410	ENSG00000109083			Ift20 (MGI:1915585)			
chr17	28335521	28347008	17q22-q23	17q11.2		191161	TNFAIP1	"Tumor necrosis factor, alpha-induced protein-1 (endothelial)"	TNFAIP1	7126	ENSG00000109079			Tnfaip1 (MGI:104961)			
chr17	28346627	28357588	17q11.2	17q11.2		611519	"POLDIP2, PDIP38"	Polymerase delta-interacting protein 2	POLDIP2	26073	ENSG00000004142			Poldip2 (MGI:1915061)			
chr17	28357580	28363682	17q11.2	17q11.2		616815	"TMEM199, VMA12, VPH2, C17orf32, CDG2P"	Transmembrane protein 199	TMEM199	147007	ENSG00000244045		"Congenital disorder of glycosylation, type IIp, 616829 (3), Autosomal recessive"	Tmem199 (MGI:2144113)			
chr17	28364267	28365150	17q11.2	17q11.2		610975	"SEBOX, OG9"	"Skin-, embryo-, brain-, and oocyte-specific homeobox"	SEBOX	645832	ENSG00000274529			Sebox (MGI:108012)			
chr17	28367276	28370351	17q11	17q11.2		193190	"VTN, VNT"	"Vitronectin (serum spreading factor, somatomedin B, complement S-protein)"	VTN	7448	ENSG00000109072			Vtn (MGI:98940)			
chr17	28371661	28401044	17q11	17q11.2		607732	"SARM, KIAA0524"	Sterile alpha and heat/armadillo motifs-containing protein	SARM1	23098	ENSG00000004139			Sarm1 (MGI:2136419)			
chr17	28394641	28406629	17q11.1	17q11.2		611672	"SLC46A1, HCP1, PCFT"	"Solute carrier family 46 (folate transporter), member 1"	SLC46A1	113235	ENSG00000076351		"Folate malabsorption, hereditary, 229050 (3), Autosomal recessive"	Slc46a1 (MGI:1098733)			
chr17	28473356	28497780	17p11.1-q11.1	17q11.2		604148	"SLC13A2, NADC1"	"Solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2"	SLC13A2	9058	ENSG00000007216			Slc13a2 (MGI:1276558)			
chr17	28506210	28538899	17q11-q12	17q11.2		600838	"FOXN1, WHN"	Forkhead box N1 (winged helix nude)	FOXN1	8456	ENSG00000109101		"T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3), Autosomal recessive"	Foxn1 (MGI:102949)			
chr17	28546706	28552662	17q11.2	17q11.2		604011	"UNC119, HRG4, IMD13"	"Unc119, C. elegans, homolog of (human retinal gene 4)"	UNC119	9094	ENSG00000109103	mutation identified in 1 IMD13 family and CORD family	"?Cone-rod dystrophy (3); ?Immunodeficiency 13, 615518 (3), Autosomal dominant"	Unc119 (MGI:1328357)			
chr17	28553387	28571868	17q11.2	17q11.2		610271	PIGS	"Phosphatidylinositol glycan, class S"	PIGS	94005	ENSG00000087111			Pigs (MGI:2687325)			
chr17	28573114	28576962	17cen-q12	17q11.2		103870	ALDOC	"Aldolase C, fructose-bisphosphatase"	ALDOC	230	ENSG00000109107			Aldoc (MGI:101863)			
chr17	28577564	28599037	17q11.2	17q11.2		615562	"SPAG5, MAP126, ASTRIN"	Sperm-associated antigen 5	SPAG5	10615	ENSG00000076382			Spag5 (MGI:1927470)			
chr17	28648355	28662188	17q11.2	17q11.2		602934	SDF2	Stromal cell-derived factor-2	SDF2	6388	ENSG00000132581			Sdf2 (MGI:108019)			
chr17	28662182	28702683	17q11.2	17q11.2		601333	SUPT6H	"Suppressor of Ty, S.cerevisiae, 6 homolog of"	SUPT6H	6830	ENSG00000109111			Supt6 (MGI:107726)			
chr17	28703196	28712064	17q11.2	17q11.2		617376	PROCA1	Proline-rich cyclin A1-interacting protein	PROCA1	147011	ENSG00000167525			Proca1 (MGI:1918274)			
chr17	28714280	28718439	17q11.1	17q11.2		610917	"RAB34, RAH"	Ras-associated protein 34	RAB34	83871	ENSG00000109113			Rab34 (MGI:104606)			
chr17	28719981	28724355	17q11	17q11.2		602326	RPL23A	Ribosomal protein L23a	RPL23A	6147	ENSG00000198242						
chr17	28727898	28742765	17q11.1	17q11.2		609799	"NEK8, JCK, NPHP9, RHPD2"	Never in mitosis gene A-related kinase 8	NEK8	284086	ENSG00000160602	mutations identified in 1 family with NPHP9	"?Nephronophthisis 9, 613824 (3); Renal-hepatic-pancreatic dysplasia 2, 615415 (3), Autosomal recessive"	Nek8 (MGI:1890646)			
chr17	28744003	28750957	17q11.2	17q11.2		602464	"TRAF4, MLN62, CART1"	TNF receptor-associated factor 4	TRAF4	9618	ENSG00000076604			Traf4 (MGI:1202880)			
chr17	28854956	28861066	17q11.2	17q11.2		607435	"ERAL1, ERAL1A, ERAL1B, PRLTS6"	ERA G-protein-like 1	ERAL1	26284	ENSG00000132591		"Perrault syndrome 6, 617565 (3), Autosomal recessive"	Eral1 (MGI:1889295)			
chr17	28861368	28861439	17q11.2	17q11.2		612071	"MIR451, MIRN451"	Micro RNA 451	MIR451A	574411							
chr17	28861532	28861617	17q11.2	17q11.2		612070	"MIR144, MIRN144"	Micro RNA 144	MIR144	406936							
chr17	28879334	28897735	17q11-q12	17q11.2		131560	"FLOT2, M17S1, ECS1, ESA1"	Flotillin 2 (epidermal surface antigen 1)	FLOT2	2319	ENSG00000132589	~180kb centromeric to NF1		Flot2 (MGI:103309)			
chr17	28897780	28903070	17q11.2	17q11.2		616157	"DHRS13, SDR7C5"	"Short-chain dehydrogenase reductase family, member 13"	DHRS13	147015	ENSG00000167536			Dhrs13 (MGI:1917701)			
chr17	28954904	29006439	17q11.2	17q11.2		616666	"SEZ6, BSRPC"	"Seizure-related 6, mouse, homolog of"	SEZ6	124925	ENSG00000063015			Sez6 (MGI:104745)			
chr17	29073509	29180388	17q11.2	17q11.2		610067	"MYO18A, SPR210"	Myosin XVIIIA	MYO18A	399687	ENSG00000196535			Myo18a (MGI:2667185)			
chr17	29073520	29075608	17q11.2	17q11.2		609517	"TIAF1, MYO18A, MYSPDZ, MAJN, SPR210, KIAA0216"	TGFB1-induced antiapoptotic factor 1	TIAF1	9220	ENSG00000221995						
chr17	29246856	29254493	17q11.1-q12	17q11.2		123610	"CRYBA1, CRYB1, CTRCT10"	"Crystallin, beta A1"	CRYBA1	1411	ENSG00000108255	centromeric to NF1	"Cataract 10, multiple types, 600881 (3), Autosomal dominant"	Cryba1 (MGI:88518)			
chr17	29255835	29294147	17q11.2	17q11.2		609356	"NUFIP2, KIAA1321, PIG1"	Nuclear fragile X mental retardation protein-interacting protein 2	NUFIP2	57532	ENSG00000108256			Nufip2 (MGI:1915814)			
chr17	29390924	29551903	17q11.2	17q11.2		610266	"TAOK1, PSK2, TAO1, MARKK"	TAO kinase 1	TAOK1	57551	ENSG00000160551			Taok1 (MGI:1914490)			
chr17	29573468	29589591	17p11.2	17q11.2		608434	GIT1	G protein-coupled receptor kinase-interacting protein 1	GIT1	28964	ENSG00000108262			Git1 (MGI:1927140)			
chr17	29589768	29615005	17q11.2	17q11.2		615124	ANKRD13B	Ankyrin repeat domain-containing protein 13B	ANKRD13B	124930	ENSG00000198720			Ankrd13b (MGI:2144501)			
chr17	29625937	29930238	17q11.2	17q11.2		606779	"SSH2, KIAA1725"	"Slingshot, Drosophila, homolog of, 2"	SSH2	85464	ENSG00000141298			Ssh2 (MGI:2679255)			
chr17	30116806	30186474	17q11.2	17q11.2		616173	"NSRP1, NSRP70, CCDC55"	Nuclear speckle splicing regulatory protein 1	NSRP1	84081	ENSG00000126653			Nsrp1 (MGI:2144305)			
chr17	30194318	30235967	17q11.1-q12	17q11.2		182138	"SLC6A4, HTT, OCD1"	"Solute carrier family 6 (neurotransmitter transporter, serotonin), member 4"	SLC6A4	6532	ENSG00000108576		"{Anxiety-related personality traits}, 607834 (3); {Obsessive-compulsive disorder}, 164230 (3), Autosomal dominant"	Slc6a4 (MGI:96285)			
chr17	30248194	30292165	17q11.2	17q11.2		602403	"BLMH, BMH"	Bleomycin hydrolase	BLMH	642	ENSG00000108578			Blmh (MGI:1345186)			
chr17	30378923	30469656	17p11.1-q11.1	17q11.2		603102	CPD	Carboxypeptidase D	CPD	1362	ENSG00000108582			Cpd (MGI:107265)			
chr17	30477401	30526813	17q11	17q11.2		604026	"GOSR1, GOS28, GS28"	Golgi snap receptor complex member 1	GOSR1	9527	ENSG00000108587			Gosr1 (MGI:1858260)			
chr17	30782683	30824759	17q11.2	17q11.2		614853	"CRLF3, CYTOR4, CRLM9, CREME9"	Cytokine receptor-like factor 3	CRLF3	51379	ENSG00000176390			Crlf3 (MGI:1860086)			
chr17	30830829	30895868	17q11.2	17q11.2		609534	"ATAD5, C17orf41, FRAG1, FLJ12735"	"ATPase family, AAA domain containing 5"	ATAD5	79915	ENSG00000176208			Atad5 (MGI:2442925)			
chr17	30898982	30907628	17q11.2	17q11.2		616422	"TEFM, C17orf42"	"Transcription elongation factor, mitochondrial"	TEFM	79736	ENSG00000172171			Tefm (MGI:1915800)			
chr17	30921735	30959397	17q11.2	17q11.2		608635	"ADAP2, CENTA2"	ArfGAP with dual PH domains 2	ADAP2	55803	ENSG00000184060			Adap2 (MGI:2663075)			
chr17	30968641	30999910	17q11	17q11.2		611358	"RNF135, MMFD"	Ring finger protein 135	RNF135	84282	ENSG00000181481		"Macrocephaly, macrosomia, facial dysmorphism syndrome, 614192 (3)"	Rnf135 (MGI:1919206)			
chr17	31094926	31377676	17q11.2	17q11.2		613113	"NF1, VRNF, WSS, NFNS"	"Neurofibromin (neurofibromatosis, type I)"	NF1	4763	ENSG00000196712		"Leukemia, juvenile myelomonocytic, 607785 (3), Autosomal dominant, Somatic mutation; Neurofibromatosis, familial spinal, 162210 (3), Autosomal dominant; Neurofibromatosis, type 1, 162200 (3), Autosomal dominant; Neurofibromatosis-Noonan syndrome, 601321 (3), Autosomal dominant; Watson syndrome, 193520 (3), Autosomal dominant"	Nf1 (MGI:97306)			
chr17	31294649	31297361	17q11.2	17q11.2		164345	"OMG, OMGP"	Oligodendrocyte-myelin glycoprotein	OMG	4974	ENSG00000126861	within the NF1 gene		Omg (MGI:106586)			
chr17	31303769	31314148	17q11.2	17q11.2		158381	"EVI2B, EVDB"	Ecotropic viral integration site 2B	EVI2B	2124	ENSG00000185862	within the NF1 gene		"Evi2,Evi2b (MGI:5439444,MGI:1890682)"			
chr17	31316409	31321748	17q11.2	17q11.2		158380	"EVI2A, EVI2, EVDA"	Ecotropic viral integration site 2A	EVI2A	2123	ENSG00000126860	within the NF1 gene		Evi2a (MGI:95458)			
chr17	31391623	31538216	17q11.2	17q11.2		611999	"RAB11FIP4, KIAA1821"	RAB11 family-interacting protein 4	RAB11FIP4	84440	ENSG00000131242			Rab11fip4 (MGI:2442920)			
chr17	31559995	31560082	17q11.2	17q11.2		614733	MIR193A	Micro RNA 193A	MIR193A	406968							
chr17	31937009	32001044	17q11.2	17q11.2		606245	"JJAZ1, KIAA0160"	JJAZ1 gene	SUZ12	23512	ENSG00000178691			Suz12 (MGI:1261758)			
chr17	32007871	32053499	17q11.2	17q11.2		616558	LRRC37B	Leucine-rich repeat-containing protein 37B	LRRC37B	114659	ENSG00000185158						
chr17	32142453	32253373	17q11.2	17q11.2		613888	"RHOT1, MIRO1, ARHT1"	"Ras homolog gene family, member T1"	RHOT1	55288	ENSG00000126858			Rhot1 (MGI:1926078)			
chr17	32350137	32381884	17q11.2	17q11.2		603428	ZNF207	Zinc finger protein-207	ZNF207	7756	ENSG00000010244	mapped by FISH to 6p21.3		Zfp207 (MGI:1340045)			
chr17	32444462	32483318	17q11.2	17q11.2		604449	"PSMD11, S9"	"Proteasome 26S subunit, non-ATPase, 11"	PSMD11	5717	ENSG00000108671			Psmd11 (MGI:1916327)			
chr17	32485027	32491255	17q11.2	17q11.2		603460	"CDK5R1, p35"	"Cyclin-dependent kinase 5, regulatory subunit 1"	CDK5R1	8851	ENSG00000176749			Cdk5r1 (MGI:101764)			
chr17	32492521	32877172	17q11-q12	17q11.2		606539	"MYO1D, KIAA0727"	Myosin ID	MYO1D	4642	ENSG00000176658			Myo1d (MGI:107728)			
chr17	32927909	32941648	17q11.2	17q11.2		615949	"TMEM98, NNO4"	Transmembrane protein 98	TMEM98	26022	ENSG00000006042		"Nanophthalmos 4, 615972 (3), Autosomal dominant"	Tmem98 (MGI:1923457)			
chr17	32991863	32997876	17q12	17q11.2		612749	"SPACA3, LYZL3, SLLP1, LYC3, ALLP17"	Sperm acrosome-associated 3	SPACA3	124912	ENSG00000141316			Spaca3 (MGI:1922872)			
chr17	33013086	34156805	17q11.2-q12	17q11-q12		601784	"ACCN1, BNC1, MDEG"	"Amiloride-sensitive cation channel 1, neuronal (degenerin)"	ASIC2	40	ENSG00000108684			Asic2 (MGI:1100867)			
chr17	33500000	39800000	17q12			603782	"CCL4L, SCYA4L, LAG1"	"Chemokine, C-C motif, ligand 4-like"	CCL4L1	388372	ENSG00000276070						
chr17	33500000	39800000	17q12			614527	"DEL17q12, C17DELq12"	Chromosome 17q12 deletion syndrome					"Chromosome 17q12 deletion syndrome, 614527 (4), Autosomal dominant"				
chr17	33500000	39800000	17q12			614526	"DUP17q12, C17DUPq12"	Chromosome 17q12 duplication syndrome					"Chromosome 17q12 duplication syndrome, 614526 (4), Autosomal dominant"				
chr17	33500000	39800000	17q12			611955	HPC11	"Prostate cancer, hereditary, 11"				associated with rs4430796 and rs7501939	"{Prostate cancer, hereditary, 11}, 611955 (2)"				
chr17	33500000	39800000	17q12			614221	PBC5	"Biliary cirrhosis, primary, 5"		100689212		associated with rs9303277	"Biliary cirrhosis, primary, 5, 614221 (2)"				
chr17	33500000	52100000	17q12-q21			601363	WT4	Wilms tumor-4		8151			"Wilms tumor, type 4, 601363 (2), Autosomal dominant"				
chr17	34255276	34257202	17q11.2-q12	17q12		158105	"CCL2, SCYA2, MCP1, MCAF"	"Small inducible cytokine A2 (monocyte chemotactic protein, homologous to mouse Sig-je)"	CCL2	6347	ENSG00000108691		"{Coronary artery disease, modifier of} (3); {HIV-1, resistance to}, 609423 (3); {Mycobacterium tuberculosis, susceptibility to}, 607948 (3); {Spina bifida, susceptibility to}, 182940 (3), Autosomal dominant"	Ccl12 (MGI:108224)			
chr17	34270215	34272241	17q11.2-q12	17q12		158106	"CCL7, SCYA7, MCP3"	"Chemokine, C-C motif, ligand 5"	CCL7	6354	ENSG00000108688	close to ERBB2					
chr17	34285667	34288179	17q21.1-q21.2	17q12		601156	"CCL11, SCYA11"	"Chemokine, C-C motif, ligand 11"	CCL11	6356	ENSG00000172156		"{Asthma, susceptibility to}, 600807 (3), Autosomal dominant; {HIV1, resistance to}, 609423 (3)"	Ccl11 (MGI:103576)			
chr17	34319046	34321401	17q11.2	17q12		602283	"CCL8, SCYA8"	"Chemokine, C-C motif, ligand 8"	CCL8	6355	ENSG00000108700						
chr17	34356451	34358609	17q11.2	17q12		601391	"CCL13, SCYA13, NCC1"	"Chemokine, C-C motif, ligand 13"	CCL13	6357	ENSG00000181374			Ccl2 (MGI:98259)			
chr17	34360327	34363232	Chr.17	17q12		182281	"CCL1, SCYA1"	"Chemokine, C-C motif, ligand 1"	CCL1	6346	ENSG00000108702			Ccl1 (MGI:98258)			
chr17	34580748	34639317	17q12	17q12		616178	TMEM132E	Transmembrane protein 132E	TMEM132E	124842	ENSG00000181291			Tmem132e (MGI:2685490)			
chr17	34927858	34981221	17q12	17q12		610730	"CCT6B, CCTZ2"	"Chaperonin containing T-complex polypeptide 1, subunit 6B"	CCT6B	10693	ENSG00000132141			Cct6b (MGI:1329013)			
chr17	34980497	35005827	17q11.2-q12	17q12		600940	LIG3	"Ligase III, DNA, ATP-dependent"	LIG3	3980	ENSG00000005156			Lig3 (MGI:109152)			
chr17	35009111	35089328	17q12	17q12		609735	RFFL	Ring finger and FYVE-like domain containing 1 (rififylin)	RFFL	117584	ENSG00000092871			Rffl (MGI:1914588)			
chr17	35099791	35119868	17q11	17q12		602954	"RAD51D, RAD51L3, BROVCA4"	"RAD51, S. cerevisiae, homolog of, D"	RAD51D	5892	ENSG00000185379		"{Breast-ovarian cancer, familial, susceptibility to, 4}, 614291 (3)"	Rad51d (MGI:1261809)			
chr17	35147792	35189344	17q11	17q12		611220	"UNC45B, SMUNC45, CTRCT43"	"UNC45, C. elegans, homolog of, B"	UNC45B	146862	ENSG00000141161	mutation identified in 1 CTRCT43 family	"?Cataract 43, 616279 (3), Autosomal dominant"	Unc45b (MGI:2443377)			
chr17	35243035	35273654	17q12	17q12		614952	SLFN5	"Schlafen family, member 5"	SLFN5	162394	ENSG00000166750			Slfn5 (MGI:1329004)			
chr17	35350304	35373913	17q12	17q12		614953	SLFN11	"Schlafen family, member 11"	SLFN11	91607	ENSG00000172716						
chr17	35407170	35433309	17q12	17q12		614955	SLFN12	"Schlafen family, member 12"	SLFN12	55106	ENSG00000172123						
chr17	35435095	35522292	17q12	17q12		614957	SLFN13	"Schlafen family, member 13"	SLFN13	146857	ENSG00000154760			"Slfn8,Slfn9 (MGI:2672859,MGI:2445121)"			
chr17	35474905	35537860	17q12	17q12		614956	SLFN12L	"Schlafen family, member 12-like"	SLFN12L	100506736	ENSG00000205045			"Slfn3,Slfn4 (MGI:1329005,MGI:1329010)"			
chr17	35545731	35560840	17q12	17q12		614958	"SLFN14, BDPLT20"	"Schlafen family, member 14"	SLFN14	342618	ENSG00000236320		"Bleeding disorder, platelet-type, 20, 616913 (3), Autosomal dominant"	Slfn14 (MGI:2684866)			
chr17	35574794	35578636	17q12	17q12		601758	"PEX12, PBD3A"	Peroxisome biogenesis factor 12	PEX12	5193	ENSG00000108733		"Peroxisome biogenesis disorder 3A (Zellweger), 614859 (3), Autosomal recessive; Peroxisome biogenesis disorder 3B, 266510 (3), Autosomal recessive"	Pex12 (MGI:2144177)			
chr17	35587262	35726416	17q11.2-q12	17q12		601025	"AP2B1, CLAPB1, ADTB2"	"Adaptor-related protein complex 2, beta 1 subunit"	AP2B1	163	ENSG00000006125						
chr17	35731659	35743520	17q12	17q12		612128	"RASL10B, RRP17"	"Ras-like, family 10, member B"	RASL10B	91608	ENSG00000270885			Rasl10b (MGI:2685575)			
chr17	35744510	35752877	17q12	17q12		611398	"GAS2L2, GAR17"	Growth arrest-specific 2-like 2	GAS2L2	246176	ENSG00000270765			Gas2l2 (MGI:3652048)			
chr17	35756248	35795706	17q11.2	17q12		608417	MMP28	Matrix metalloproteinase 28	MMP28	79148	ENSG00000271447			Mmp28 (MGI:2153062)			
chr17	35809454	35847241	17q11.1-q11.2	17q12		601574	"TAF15, TAF2N, RBP56"	"TAF15 RNA polymerase II, TATA box-binding protein-associated factor, 68kD"	TAF15	8148	ENSG00000270647	fusion gene with CSMF	"Chondrosarcoma, extraskeletal myxoid, 612237 (1)"	Taf15 (MGI:1917689)			
chr17	35871490	35880372	17q11.2-q12	17q12		187011	"CCL5, SCYA5, D17S136E, TCP228"	"Chemokine, C-C motif, ligand 5"	CCL5	6352	ENSG00000271503		"{HIV-1 disease, delayed progression of} (3); {HIV-1 disease, rapid progression of} (3)"	Ccl5 (MGI:98262)			
chr17	35918079	35931820	17q11.2	17q12		612896	RDM1	RAD52 motif-containing protein 1	RDM1	201299	ENSG00000278023			Rdm1 (MGI:1913849)			
chr17	35934517	35943709	17q11.2	17q12		612751	LYZL6	Lysozyme-like 6	LYZL6	57151	ENSG00000275722			Lyzl6 (MGI:1916694)			
chr17	35976492	35983619	17q11.2	17q12		601394	"CCL16, SCYA16, NCC4"	"Chemokine, C-C motif, ligand 16"	CCL16	6360	ENSG00000275152						
chr17	35983655	35986727	17q11.2	17q12		601392	"CCL14, SCYA14, NCC2"	"Chemokine, C-C motif, ligand 14"	CCL14	6358	ENSG00000276409						
chr17	35997581	36002037	17q11.2	17q12		601393	"CCL15, SCYA15, NCC3, LKN1"	"Chemokine, C-C motif, ligand 15"	CCL15	6359	ENSG00000275718						
chr17	36013055	36018178	17q12	17q12		602494	"CCL23, SCYA23"	"Chemokine, C-C motif, ligand 23"	CCL23	6368	ENSG00000274736						
chr17	36064271	36071480	17q11.2	17q12		603757	"CCL18, SCYA18, PARC, AMAC1, DCCK1"	"Chemokine, C-C motif, ligand 18"	CCL18	6362	ENSG00000275385	"in 47kb, CCL18-CCL3-CCL4"					
chr17	36088255	36090159	17q12	17q12		182283	"CCL3, SCYA3, MIP1A"	"Chemokine, C-C motif, ligand 3"	CCL3	6348	ENSG00000277632	"in 47kb, CCL18-CCL3-CCL4"	"{HIV infection, resistance to}, 609423 (2)"				
chr17	36103826	36105620	17q12	17q12		182284	"CCL4, SCYA4, ACT2, MIP1B, AT744.1"	"Chemokine, C-C motif, ligand 4"	CCL4	6351	ENSG00000275302			Ccl4 (MGI:98261)			
chr17	36165680	36176623	17q12	17q12		610144	"TBC1D3B, PRC17"	"TBC1 domain family, member 3B"	TBC1D3B	414059	ENSG00000274808						
chr17	36211062	36212877	17q12	17q12		610757	CCL4L2	"Chemokine, CC motif, ligand 4-like 2"	CCL4L2	9560	ENSG00000276070						
chr17	36322241	36334758	17q12	17q12		610810	TBC1D3G	"TBC1 domain family, member 3G"	TBC1D3G	101060321	ENSG00000260287						
chr17	36377474	36388451	17q12	17q12		610811	TBC1D3H	"TBC1 domain family, member 3H"	TBC1D3H	729877	ENSG00000274226						
chr17	36428611	36439522	17q12	17q12		610809	TBC1D3F	"TBC1 domain family, member 3F"	TBC1D3F	84218	ENSG00000275954						
chr17	36486626	36499309	17q12	17q12		604500	"ZNHIT3, TRIP3, PEHO"	Zinc finger HIT domain-containing protein 3	ZNHIT3	9326	ENSG00000273611		"PEHO syndrome, 260565 (3), Autosomal recessive"	Znhit3 (MGI:3051596)			
chr17	36495635	36535456	17q12	17q12		617379	"MYO19, MYOHD1"	Myosin XIX	MYO19	80179	ENSG00000278259			Myo19 (MGI:1913446)			
chr17	36534761	36539302	17q12	17q12		610275	"PIGW, HPMRS5"	"Phosphatidylinositol glycan, class W"	PIGW	284098	ENSG00000277161		"Glycosylphosphatidylinositol biosynthesis defect 11, 616025 (3), Autosomal recessive"	Pigw (MGI:1917575)			
chr17	36544887	36589847	17q12-q21.1	17q12		612275	"GGNBP2, DIF3, LCRG1, LZK1"	Gametogenetin-binding protein 2	GGNBP2	79893	ENSG00000278311			Ggnbp2 (MGI:2387356)			
chr17	36591795	36600803	17q12	17q12		616159	"DHRS11, SDR24C1"	"Short-chain dehydrogenase reductase family, member 11"	DHRS11	79154	ENSG00000278535			Dhrs11 (MGI:2652816)			
chr17	36937474	36944614	17q12	17q12		601999	"LHX1, LIM1"	LIM/homeodomain protein LHX1	LHX1	3975	ENSG00000273706	previously mapped to 11p13-p12 by FISH		Lhx1 (MGI:99783)			
chr17	36948874	37056870	17q11.2-q12	17q12		608463	"AATF, CHE1"	Apoptosis-antagonizing transcription factor	AATF	26574	ENSG00000275700			Aatf (MGI:1929608)			
chr17	37084991	37406821	17q21	17q12		200350	"ACACA, ACAC, ACC1, ACACAD"	"Acetyl-Coenzyme A carboxylase, alpha"	ACACA	31	ENSG00000278540	proximal to q21.33; others put at 17q12	"Acetyl-CoA carboxylase deficiency, 613933 (1), Autosomal recessive"	Acaca (MGI:108451)			
chr17	37406876	37479724	17q12-q21	17q12		602276	"TADA2L, TADA2A, ADA2A"	Transcriptional adaptor 2A	TADA2A	6871	ENSG00000276234			Tada2a (MGI:2144471)			
chr17	37488560	37513500	Chr.17	17q12		606618	"DUSP14, MKP6"	Dual-specificity phosphatase 14	DUSP14	11072	ENSG00000276023			Dusp14 (MGI:1927168)			
chr17	37514796	37609495	Chr.17	17q12		607291	"AP1GBP1, SYNG"	Adaptor-related protein complex 1 gamma subunit-binding protein 1	SYNRG	11276	ENSG00000275066			Synrg (MGI:1354742)			
chr17	37609738	37643463	17q21.1	17q12		612500	"DDX52, ROK1, HUSSY19"	DEAD box polypeptide 52	DDX52	11056	ENSG00000278053			Ddx52 (MGI:1925644)			
chr17	37686430	37745077	17q12	17q12		189907	"HNF1B, TCF2, HNF2, MODY5, FJHN, HPC11"	HNF1 homeobox B (transcription factor 2)	HNF1B	6928	ENSG00000275410		"Diabetes mellitus, noninsulin-dependent, 125853 (3), Autosomal dominant; {Renal cell carcinoma}, 144700 (3); Renal cysts and diabetes syndrome, 137920 (3), Autosomal dominant"	Hnf1b (MGI:98505)			
chr17	38004032	38014907	17q12	17q12		610807	TBC1D3D	"TBC1 domain family, member 3D"	TBC1D3D	101060389	ENSG00000274419						
chr17	38057692	38068633	17q12	17q12		610806	TBC1D3C	"TBC1 domain family, member 3C"	TBC1D3C	414060	ENSG00000274808						
chr17	38118407	38138867	17q12	17q12		610808	TBC1D3E	"TBC1 domain family, member 3E"	TBC1D3E	102723859	ENSG00000273513						
chr17	38181475	38192554	17q12	17q12		607741	"TBC1D3, PRC17, TBC1D3A"	TBC1D3 gene	TBC1D3	729873	ENSG00000274512						
chr17	38297022	38323217	17q21.31	17q12		611850	MRPL45	Mitochondrial ribosomal protein L45	MRPL45	84311	ENSG00000278845	pseudogenes on 2 and 17		Mrpl45 (MGI:1914286)			
chr17	38325609	38343809	17q12	17q12		614515	"GPR179, GPR158L, GPR158L1, CSNB1E"	G protein-coupled receptor 179	GPR179	440435	ENSG00000277399		"Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3), Autosomal recessive"	Gpr179 (MGI:2443409)			
chr17	38419285	38512391	17q12	17q12		610590	"ARHGAP23, KIAA1501"	RHO GTPase-activating protein 23	ARHGAP23	57636	ENSG00000275832			Arhgap23 (MGI:3697726)			
chr17	38530014	38607165	17q12	17q12		610786	"SRCIN1, SNIP, KIAA1684"	Src kinase signaling inhibitor 1	SRCIN1	80725	ENSG00000277363			Srcin1 (MGI:1933179)			
chr17	38671702	38674933	17q12	17q12		617795	"EPOP, C17orf96"	Elongin BC- and polycomb repressive complex 2-associated protein	EPOP	100170841	ENSG00000273604			Epop (MGI:2143991)			
chr17	38705619	38729802	17q21	17q12		600328	"MLLT6, AF17"	"Myeloid/lymphoid or mixed-lineage leukemia, translocated to, 6"	MLLT6	4302	ENSG00000275023			Mllt6 (MGI:1935145)			
chr17	38730256	38735604	17q12	17q12		611933	"CISD3, MINER2"	CDGSH iron sulfur domain protein 3	CISD3	284106	ENSG00000277972			"Cisd3b,Cisd3 (MGI:5012452,MGI:101788)"			
chr17	38733896	38749816	17q12	17q12		600346	"RNF110, ZNF144, MEL18"	Ring finger protein 110 (zinc finger protein-144)	PCGF2	7703	ENSG00000277258	previously assigned to 12q22		Pcgf2 (MGI:99161)			
chr17	38752712	38764230	17q12	17q12		602176	PSMB3	"Proteasome subunit, beta type, 3"	PSMB3	5691	ENSG00000277791	previously assigned to 2q35		Psmb3 (MGI:1347014)			
chr17	38765690	38799904	17q12	17q12		603261	"PIP4K2B, PIP5P4KB, PIP5K2B"	"Phosphatidylinositol 5-phosphate 4-kinase, type II, beta"	PIP4K2B	8396	ENSG00000276293			Pip4k2b (MGI:1934234)			
chr17	38850067	38853799	17q	17q12		603662	RPL23	Ribosomal protein L23	RPL23	9349	ENSG00000125691			Rpl23 (MGI:1929455)			
chr17	38869858	38921769	17q21	17q12		602920	"LASP1, MLN50"	LIM and SH3 protein 1	LASP1	3927	ENSG00000002834	fused to MLL in AML		Lasp1 (MGI:109656)			
chr17	38925167	38929383	17q12	17q12		617544	LINC00672	Long intergenic noncoding RNA 672	LINC00672	100505576							
chr17	38936277	38967475	17q12	17q12		609498	FBXO47	F-box only protein 47	FBXO47	494188	ENSG00000204952			Fbxo47 (MGI:1920223)			
chr17	39063302	39151648	17q21.1	17q12		606826	"PLXDC1, TEM7"	Plexin domain containing 1	PLXDC1	57125	ENSG00000161381			Plxdc1 (MGI:1919574)			
chr17	39173455	39197702	17q21-q22	17q12		114207	"CACNB1, CACNLB1, CCHLB1"	"Calcium channel, voltage-dependent, beta 1 subunit"	CACNB1	782	ENSG00000067191			Cacnb1 (MGI:102522)			
chr17	39200282	39204729	17q11	17q12		180466	RPL19	Ribosomal protein L19	RPL19	6143	ENSG00000108298			Rpl19 (MGI:98020)			
chr17	39252643	39402658	17q21.2	17q12		609086	"FBXL20, FBL20, FBL2, SCR"	F-box and leucine-rich repeat protein 20	FBXL20	84961	ENSG00000108306			Fbxl20 (MGI:1919444)			
chr17	39404284	39451280	17q12	17q12		604311	"MED1, PPARBP, PBP, TRAP220"	Mediator complex subunit 1 (peroxisome proliferator-activated receptor-binding protein)	MED1	5469	ENSG00000125686			Med1 (MGI:1100846)			
chr17	39461485	39567559	17q21	17q12		615514	"CDK12, CRKRS, CRK7, KIAA0904"	Cyclin-dependent kinase 12	CDK12	51755	ENSG00000167258			Cdk12 (MGI:1098802)			
chr17	39603767	39607921	17q12	17q12		601725	NEUROD2	Neurogenic differentiation 2	NEUROD2	4761	ENSG00000171532			Neurod2 (MGI:107755)			
chr17	39637079	39664200	17q11-q21	17q12		607048	"STARD3, MLN64"	Start domain-containing protein 3	STARD3	10948	ENSG00000131748			Stard3 (MGI:1929618)			
chr17	39665345	39666553	17q12	17q12		604488	"TCAP, LGMD2G, CMH25"	Telethonin	TCAP	8557	ENSG00000173991		"Cardiomyopathy, hypertrophic, 25, 607487 (3), Autosomal dominant; Muscular dystrophy, limb-girdle, type 2G, 601954 (3), Autosomal recessive"	Tcap (MGI:1330233)			
chr17	39667980	39670474	17q12	17q12		171190	"PNMT, PENT"	Phenylethanolamine N-methyltransferase	PNMT	5409	ENSG00000141744			Pnmt (MGI:97724)			
chr17	39671121	39688069	17q12	17q12		611801	"PGAP3, PERLD1, CAB2, MGC9753, HPMRS4"	Post-GPI attachment to proteins 3	PGAP3	93210	ENSG00000161395		"Hyperphosphatasia with mental retardation syndrome 4, 615716 (3), Autosomal recessive"	Pgap3 (MGI:2444461)			
chr17	39688083	39728661	17q21.1	17q12		164870	"ERBB2, NGL, NEU, HER2"	Avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 2 (neuro/glioblastoma derived oncogene homolog)	ERBB2	2064	ENSG00000141736		"Adenocarcinoma of lung, somatic, 211980 (3); Gastric cancer, somatic, 613659 (3); Glioblastoma, somatic, 137800 (3); Ovarian cancer, somatic (3)"	Erbb2 (MGI:95410)			
chr17	39728499	39730562	17q12	17q12		611802	"MIEN1, C17orf37, RDX12"	Migration and invasion enhancer 1	MIEN1	84299	ENSG00000141741			Mien1 (MGI:1913678)			
chr17	39737900	39747284	17q21-q22	17q12		601522	GRB7	Growth factor receptor-bound protein 7	GRB7	2886	ENSG00000141738			Grb7 (MGI:102683)			
chr17	39757714	39864187	17q21	17q12-q21		606221	"IKZF3, ZNFN1A3, AIOLOS"	Ikaros family zinc finger 3	IKZF3	22806	ENSG00000161405			Ikzf3 (MGI:1342542)			
chr17	39800000	52100000	17q21			611403	ASRT6	"Asthma-related traits, susceptibility to, 6"		100188840		strongly associated with rs7216389	"{Asthma-related traits, susceptibility to, 6}, 611403 (2)"				
chr17	39800000	52100000	17q21			610676	AUTS7	"Autism, susceptibility to, 7"		100188816		max lod at D17S2180	"{Autism susceptibility 7}, 610676 (2)"				
chr17	39800000	59500000	17q21-q22			610997	HPC9	"Prostate cancer, hereditary, 9"		100188826		max LOD at D17S1820	"{Prostate cancer, hereditary, 9}, 610997 (2)"				
chr17	39800000	59500000	17q21-q22			608474	MYP5	Myopia 5	MYP5	404682		between D17S787 and D17S1811	"Myopia 5, 608474 (2), Autosomal dominant"				
chr17	39800000	59500000	17q21-q22			168860	"PTLAH, FPAH"	Patella aplasia or hypoplasia	PTLAH	8830			"Patella aplasia or hypoplasia, 168860 (2), Autosomal dominant"				
chr17	39868163	39877895	17q12-q21	17q21.1		608499	"ZPBP2, ZPBPL"	Zona pellucida-binding protein 2	ZPBP2	124626	ENSG00000186075			Zpbp2 (MGI:1916626)			
chr17	39904594	39918649	17q21	17q21.1		611221	"GSDMB, GSDML"	Gasdermin B	GSDMB	55876	ENSG00000073605						
chr17	39921040	39927803	17q21.1	17q21.1		610075	ORMDL3	ORM1-like protein 3	ORMDL3	94103	ENSG00000172057			Ormdl3 (MGI:1913862)			
chr17	39962972	39977765	17q12	17q21.1		611218	"GSDMA, GSDM1, GSDM"	Gasdermin A	GSDMA	284110	ENSG00000167914			Gsdma (MGI:1889509)			
chr17	39980767	39997959	17q21.1	17q21.1		617676	"PSMD3, RPN3"	"Proteasome 26S subunit, non-ATPase, 3"	PSMD3	5709	ENSG00000108344			Psmd3 (MGI:98858)			
chr17	40015360	40017812	17q11.2-q12	17q21.1		138970	"CSF3, GCSF"	Colony-stimulating factor-3 (granulocyte)	CSF3	1440	ENSG00000108342			Csf3 (MGI:1339751)			
chr17	40019096	40054741	17q21.1	17q21.1		607000	"MED24, TRAP100, KIAA0130"	Mediator complex subunit 24	MED24	9862	ENSG00000008838			Med24 (MGI:1344385)			
chr17	40062192	40093866	17q11.2	17q21.1		190120	"THRA, ERBA1, THRA1, CHNG6"	"Thyroid hormone receptor, alpha (oncogene ERBA1)"	THRA	7067	ENSG00000126351		"Hypothyroidism, congenital, nongoitrous, 6, 614450 (3), Autosomal dominant"	Thra (MGI:98742)			
chr17	40092783	40100724	17q11.2	17q21.1		602408	"NR1D1, THRAL, EAR1"	"Nuclear receptor 1, subfamily D, member 1 (thyroid hormone receptor, alpha-1-like)"	NR1D1	9572	ENSG00000126368			Nr1d1 (MGI:2444210)			
chr17	40121408	40136789	17q21.1	17q21.1		614801	MSL1	"Male-specific lethal 1, Drosophila, homolog of"	MSL1	339287	ENSG00000188895			Msl1 (MGI:1921276)			
chr17	40140253	40172177	17q12-q21.3	17q21.1		606504	"MLN51, CASC3"	MLN51 gene	CASC3	22794	ENSG00000108349			Casc3 (MGI:2179723)			
chr17	40200000	42800000	17q21.2			612380	IBD22	Inflammatory bowel disease 22		100240732		associated with rs744166	"{Inflammatory bowel disease 22}, 612380 (2)"				
chr17	40219303	40284135	17q21.2	17q21.2		609692	"WIRE, WICH"	WASP-interacting protein-related protein	WIPF2	147179	ENSG00000171475			Wipf2 (MGI:1924462)			
chr17	40287877	40303160	17q21.2	17q21.2		602627	"CDC6, CDC18L, MGORS5"	"Cell division cycle 6, S. cerevisiae, homolog of"	CDC6	990	ENSG00000094804	mutation identified in 1 MGORS5 patient	"?Meier-Gorlin syndrome 5, 613805 (3), Autosomal recessive"	Cdc6 (MGI:1345150)			
chr17	40309170	40357642	17q21.1	17q21.2		180240	RARA	"Retinoic acid receptor, alpha polypeptide"	RARA	5914	ENSG00000131759	fused with MYL in APL	"Leukemia, acute promyelocytic, 612376 (1)"	Rara (MGI:97856)			
chr17	40360651	40364692	17q21.1	17q21.2		607425	"GJD3, GJC1, CX31.9"	"Gap junction protein, delta-3 (31.9kD)"	GJD3	125111	ENSG00000183153			Gjd3 (MGI:2384150)			
chr17	40388520	40417949	17q21-q22	17q21.2		126430	"TOP2A, TOP2"	"Topoisomerase (DNA) II, alpha, 170kD"	TOP2A	7153	ENSG00000131747		"DNA topoisomerase II, resistance to inhibition of, by amsacrine (3)"	Top2a (MGI:98790)			
chr17	40443423	40457729	17q12-q21	17q21.2		146733	IGFBP4	Insulin-like growth factor-binding protein-4	IGFBP4	3487	ENSG00000141753			Igfbp4 (MGI:96439)			
chr17	40475827	40501680	17q12-q21	17q21.2		608385	"TNS4, CTEN"	Tensin 4	TNS4	84951	ENSG00000131746			Tns4 (MGI:2144377)			
chr17	40553768	40565483	17q12-q21.2	17q21.2		600242	"CCR7, CMKBR7, EBI1"	Chemokine (C-C) receptor 7 (Epstein-Barr virus induced gene 1)	CCR7	1236	ENSG00000126353			Ccr7 (MGI:103011)			
chr17	40627719	40647850	17q21.2	17q21.2		603111	"SMARCE1, BAF57, CSS5"	"SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily E, member 1"	SMARCE1	6605	ENSG00000073584		"Coffin-Siris syndrome 5, 616938 (3), Autosomal dominant; {Meningioma, familial, susceptibility to}, 607174 (3), Autosomal dominant"	Smarce1 (MGI:1927347)			
chr17	40694245	40703749	17q11.2	17q21.2		607742	"KRT24, FLJ20261"	Keratin 24	KRT24	192666	ENSG00000167916			Krt24 (MGI:1922956)			
chr17	40748020	40755541	17q21.2	17q21.2		616646	"KRT25, K25, KRT24IRS1, ARWH3"	"Keratin 25, type I"	KRT25	147183	ENSG00000204897		"Woolly hair, autosomal recessive 3, 616760 (3), Autosomal recessive"	Krt25 (MGI:1918060)			
chr17	40766237	40772158	17q21.2	17q21.2		616675	"KRT26, K25, K25B, K25IRS2"	"Keratin 26, type I"	KRT26	353288	ENSG00000186393			Krt26 (MGI:2444913)			
chr17	40776807	40782533	17q21.2	17q21.2		616676	"KRT27, KRT25C, K25IRS3"	"Keratin 27, type I"	KRT27	342574	ENSG00000171446			Krt27 (MGI:1339999)			
chr17	40792195	40799958	17q21.2	17q21.2		616677	"KRT28, K25D, K25IRS4"	"Keratin 28, type I"	KRT28	162605	ENSG00000173908			Krt28 (MGI:1918093)			
chr17	40818116	40822620	17q21-q22	17q21.2		148080	"KRT10, EHK, BCIE, BIE"	Keratin 10	KRT10	3858	ENSG00000186395	in cluster of class I keratins	"Epidermolytic hyperkeratosis, 113800 (3), Autosomal recessive, Autosomal dominant; Ichthyosis with confetti, 609165 (3), Autosomal dominant; Ichthyosis, cyclic, with epidermolytic hyperkeratosis, 607602 (3), Autosomal dominant"				
chr17	40861177	40867209	17q12	17q21.2		601687	KRT12	Keratin 12	KRT12	3859	ENSG00000187242		"Meesmann corneal dystrophy, 122100 (3), Autosomal dominant"	Krt12 (MGI:96687)			
chr17	40875888	40885242	17q12-q21	17q21.2		608218	"KRT20, CD20, KRT21"	Keratin 20	KRT20	54474	ENSG00000171431			Krt20 (MGI:1914059)			
chr17	40922695	40937642	17q21.2	17q21.2		606194	KRT23	Keratin 23	KRT23	25984	ENSG00000108244			Krt23 (MGI:2148866)			
chr17	40958416	40966891	17q21.2	17q21.2		616678	KRT39	"Keratin 38, type I"	KRT39	390792	ENSG00000196859			Krt39 (MGI:3588208)			
chr17	40977715	40987134	17q21.2	17q21.2		616679	"KRT40, KA36"	"Keratin 40, type I"	KRT40	125115	ENSG00000204889			Krt40 (MGI:3629968)			
chr17	41026025	41027201	17q12-q21	17q21.2		608822	"KRTAP-15, KAP1.5"	Keratin-associated protein 1-5	KRTAP1-5	83895	ENSG00000221852			Krtap1-4 (MGI:3651229)			
chr17	41029676	41030124	17q12-q21	17q21.2		608821	"KRTAP1-4, KAP1.4"	Keratin-associated protein 1-4	KRTAP1-4	728255	ENSG00000204887						
chr17	41033883	41034854	17q12-q21	17q21.2		608820	"KRTAP1-3, KAP1.3, KAP1.2, KAP1.9"	Keratin-associated protein 1-3	KRTAP1-3	81850	ENSG00000221880			Krtap9-3 (MGI:1922836)			
chr17	41040558	41041460	17q12-q21	17q21.2		608819	"KRTAP1-1, KAP1.1, KAP1.7, KAP1.6"	Keratin-associated protein 1-1	KRTAP1-1	81851	ENSG00000188581			Krtap1-3 (MGI:3650443)			
chr17	41345703	41350811	17q12-q21	17q21.2		602761	"KRT33A, KRTHA3A, HA3I"	Keratin 33A	KRT33A	3883	ENSG00000006059						
chr17	41363493	41369799	17q12-q21	17q21.2		602762	"KRT33B, KRTHA3A, HA3II"	Keratin 33B	KRT33B	3884	ENSG00000131738						
chr17	41377664	41383815	17q12-q21	17q21.2		602763	"KRT34, KRTHA4, HA4"	Keratin 34	KRT34	3885	ENSG00000131737			Krt34 (MGI:1309994)			
chr17	41393723	41397591	17q12-q21	17q21.2		601077	"KRT31, KRTHA1, HA1"	Keratin 31	KRT31	3881	ENSG00000094796			"Krt33b,Krt33a,Krt31 (MGI:1919138,MGI:1309993,MGI:1309991)"			
chr17	41420556	41424569	17q12-q21	17q21.2		604541	"KRT37, KRTHA7, HA7"	Keratin 37	KRT37	8688	ENSG00000108417						
chr17	41436368	41441343	17q12-q21	17q21.2		604542	"KRT38,  KRTHA8, HA8"	Keratin 38	KRT38	8687	ENSG00000171360						
chr17	41459512	41469251	17q12-q21	17q21.2		602760	"KRT32, KRTHA2, HA2"	Keratin 32	KRT32	3882	ENSG00000108759			Krt32 (MGI:1309995)			
chr17	41476688	41482742	17q12-q21	17q21.2		602764	"KRT35, KRTHA5"	Keratin 35	KRT35	3886	ENSG00000197079			Krt35 (MGI:1858899)			
chr17	41486135	41489863	17q12-q21	17q21.2		604540	"KRT36, KRTHA6, HA6"	Keratin 36	KRT36	8689	ENSG00000126337			Krt36 (MGI:109364)			
chr17	41500980	41505612	17q21.2	17q21.2		148065	"KRT13, WSN2"	Keratin 13	KRT13	3860	ENSG00000171401	"in same PFGE fragment as KRT10, KRT15"	"White sponge nevus 2, 615785 (3), Autosomal dominant"	Krt13 (MGI:101925)			
chr17	41513744	41521923	17q21-q22	17q21.2		148030	KRT15	Keratin 15	KRT15	3866		tightly linked to Hox-2 in mouse		Krt15 (MGI:96689)			
chr17	41523616	41528388	17q21-q22	17q21.2		148020	KRT19	Keratin 19	KRT19	3880	ENSG00000171345	probably 17q21-q22		Krt19 (MGI:96693)			
chr17	41565840	41572057	17q12-q21	17q21.2		607606	"KRT9, EPPK"	Keratin 9	KRT9	3857	ENSG00000171403		"Palmoplantar keratoderma, epidermolytic, 144200 (3), Autosomal dominant"				
chr17	41582278	41586894	17q12-q21	17q21.2		148066	KRT14	Keratin 14	KRT14	3861	ENSG00000186847		"Dermatopathia pigmentosa reticularis, 125595 (3), Autosomal dominant; Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3), Autosomal dominant; Epidermolysis bullosa simplex, Koebner type, 131900 (3), Autosomal dominant; Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3), Autosomal dominant; Epidermolysis bullosa simplex, recessive 1, 601001 (3), Autosomal recessive; Naegeli-Franceschetti-Jadassohn syndrome, 161000 (3), Autosomal dominant"	Krt14 (MGI:96688)			
chr17	41609777	41612826	17q12-q21	17q21.2		148067	"KRT16, FNEPPK, PC1"	Keratin 16	KRT16	3868	ENSG00000186832	probably 17q21-q22	"Pachyonychia congenita 1, 167200 (3), Autosomal dominant; Palmoplantar keratoderma, nonepidermolytic, focal, 613000 (3), Autosomal dominant"	Krt16 (MGI:96690)			
chr17	41619439	41624629	17q12-q21	17q21.2		148069	"KRT17, PC2, PCHC1"	Keratin 17	KRT17	3872	ENSG00000128422	~5' to KRT16; probably 17q21-q22	"Pachyonychia congenita 2, 167210 (3), Autosomal dominant; Steatocystoma multiplex, 184500 (3), Autosomal dominant"	Krt17 (MGI:96691)			
chr17	41712325	41715968	17q21	17q21.2		137250	"GAS, GAST"	Gastrin	GAST	2520	ENSG00000184502			Gast (MGI:104768)			
chr17	41722638	41734645	17q21.2-q21.3	17q21.2		600947	"HAP1, HLP, HAP2"	Huntingtin-associated protein 1 (neuroan 1)	HAP1	9001	ENSG00000173805			Hap1 (MGI:1261831)			
chr17	41754606	41786767	17q21	17q21.2		173325	"JUP, DP3, PDGB, ARVD12"	Junction plakoglobin	JUP	3728	ENSG00000173801	incorrectly mapped to 7; close to BRCA1	"Arrhythmogenic right ventricular dysplasia 12, 611528 (3), Autosomal dominant; Naxos disease, 601214 (3), Autosomal recessive"	Jup (MGI:96650)			
chr17	41801951	41812709	17q21.2	17q21.2		617419	"P3H4, SC65, LEPREL4"	Proyly 3-hydroxylase 4	P3H4	10609	ENSG00000141696			P3h4 (MGI:1913430)			
chr17	41812709	41823216	17q21.2	17q21.2		607063	"FKBP10, FKBP65, OI11, BRKS1"	FK506-binding protein 10	FKBP10	60681	ENSG00000141756		"Bruck syndrome 1, 259450 (3), Autosomal recessive; Osteogenesis imperfecta, type XI, 610968 (3), Autosomal recessive"	Fkbp10 (MGI:104769)			
chr17	41835684	41848367	17q21.2	17q21.2		608778	"KLHL10, SPGF11"	Kelch-like 10	KLHL10	317719	ENSG00000161594		"Spermatogenic failure 11, 615081 (3), Autosomal dominant"	Klhl10 (MGI:2181067)			
chr17	41866915	41930541	17q21.1	17q21.2		108728	ACLY	ATP citrate lyase	ACLY	47	ENSG00000131473			Acly (MGI:103251)			
chr17	41930593	41966516	17q21.2	17q21.2		617095	"TTC25, CILD35"	Tetratricopeptide repeat domain-containing protein 25	TTC25	83538	ENSG00000204815		"Ciliary dyskinesia, primary, 35, 617092 (3), Autosomal recessive"	Ttc25 (MGI:1921657)			
chr17	41966740	41977739	17q21	17q21.2		123830	"CNP, CNP1"	"2', 3' cyclic nucleotide 3' phosphohydrolase"	CNP	1267	ENSG00000173786	flanked by THRA1 and NGFR		Cnp (MGI:88437)			
chr17	41976420	42021370	17q11-q23	17q21.2		601964	"DANJC7, TTC2, TPR2"	"DnaJ, E. coli, homolog of, subfamily C, member 7 (tetratricopeptide repeat domain 2)"	DNAJC7	7266	ENSG00000168259			Dnajc7 (MGI:1928373)			
chr17	42017575	42025640	17q21.1	17q21.2		604497	"NKIRAS2, KBRAS2"	NFKB inhibitor-interacting Ras-like protein 2	NKIRAS2	28511	ENSG00000168256			Nkiras2 (MGI:1919216)			
chr17	42101403	42112732	17q21.2	17q21.2		608588	"DHX58, LGP2, D11LGP2"	DEAH (Asp-Glu-Ala-His) box polypeptide 58	DHX58	79132	ENSG00000108771			Dhx58 (MGI:1931560)			
chr17	42113110	42121408	17q21	17q21.2		602301	"KAT2A, GCN5L2, GCN5"	K(lysine) acetyltransferase 2A	KAT2A	2648	ENSG00000108773			Kat2a (MGI:1343101)			
chr17	42122737	42123352	17q21.3	17q21.2		608344	HSPB9	Heat-shock 27kD protein 9	HSPB9	94086	ENSG00000260325			Hspb9 (MGI:1922732)			
chr17	42124975	42155043	17q21.2	17q21.2		604037	"RAB5C, RABL"	Ras-associated protein RAB5c	RAB5C	5878	ENSG00000108774			Rab5c (MGI:105306)			
chr17	42184059	42185451	17q21	17q21.2		602358	"HCRT, OX, NRCLP1"	Hypocretin	HCRT	3060	ENSG00000161610	mutation identified in 1 NRCLP1 patient	"?Narcolepsy 1, 161400 (3), Autosomal dominant"	Hcrt (MGI:1202306)			
chr17	42199176	42288436	17q11.2	17q21.2		604260	STAT5B	Signal transducer and activator of transcription 5B	STAT5B	6777	ENSG00000173757	fused with RARA in PML	"Growth hormone insensitivity with immunodeficiency, 245590 (3); Leukemia, acute promyelocytic, somatic, 102578 (3)"	Stat5b (MGI:103035)			
chr17	42287546	42311942	17q21.2	17q21.2		601511	"STAT5A, STAT5, MGF"	Signal transducer and activator of transcription 5a	STAT5A	6776	ENSG00000126561			Stat5a (MGI:103036)			
chr17	42313323	42388502	17q21	17q21.2		102582	"STAT3, APRF, HIES, ADMIO1"	Signal transducer and activator of transcription-3 (acute-phase response factor)	STAT3	6774	ENSG00000168610		"Autoimmune disease, multisystem, infantile-onset, 1, 615952 (3), Autosomal dominant; Hyper-IgE recurrent infection syndrome, 147060 (3), Autosomal dominant"	Stat3 (MGI:103038)			
chr17	42402448	42423319	17q21	17q21.2		603198	"CAVIN1, PTRF"	Caveolae-associated protein 1	CAVIN1	284119	ENSG00000177469		"Lipodystrophy, congenital generalized, type 4, 613327 (3), Autosomal recessive"	Cavin1 (MGI:1277968)			
chr17	42458843	42522578	17q21	17q21.2		192130	"ATP6V0A1, ATP6N1A, VPP1"	"ATPase, H+ transporting, lysosomal, V0 subunit A1"	ATP6V0A1	535	ENSG00000033627			Atp6v0a1 (MGI:103286)			
chr17	42534237	42544448	17q21	17q21.2		609701	"NAGLU, MPS3B, CMT2V"	"N-acetylglucosaminidase, alpha-"	NAGLU	4669	ENSG00000108784	mutation identified in 1 CMT2V family	"?Charcot-Marie-Tooth disease, axonal, type 2V, 616491 (3), Autosomal dominant; Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920 (3), Autosomal recessive"	Naglu (MGI:1351641)			
chr17	42552557	42555213	17q21.2	17q21.2		109684	"HSD17B1, EDH17B2"	Estradiol 17-beta-dehydrogenase-1	HSD17B1	3292	ENSG00000108786			Hsd17b1 (MGI:105077)			
chr17	42562073	42566280	17q12-q21	17q21.2		609855	"COASY, NBIA6"	Coenzyme A synthase	COASY	80347	ENSG00000068120		"Neurodegeneration with brain iron accumulation 6, 615643 (3), Autosomal recessive"	Coasy (MGI:1918993)			
chr17	42567059	42573202	17q21.1	17q21.2		602976	"MLX, TCFL4"	MAX-like protein X	MLX	6945	ENSG00000108788			Mlx (MGI:108398)			
chr17	42572309	42577830	17q21.2	17q21.2		608665	"PSMC3IP, TBPIP, GT198, HOP2, ODG3"	PSMC3-interacting protein	PSMC3IP	29893	ENSG00000131470		"Ovarian dysgenesis 3, 614324 (3), Autosomal recessive"	Psmc3ip (MGI:1098610)			
chr17	42579507	42609426	17q21.2	17q21.2		616498	FAM134C	"Family with sequence similarity 134, member C"	RETREG3	162427	ENSG00000141699			Retreg3 (MGI:1915248)			
chr17	42609339	42615237	17q21	17q21.2		191135	"TUBG1, CDCBM4"	"Tubulin, gamma 1"	TUBG1	7283	ENSG00000131462		"Cortical dysplasia, complex, with other brain malformations 4, 615412 (3), Autosomal dominant"	Tubg1 (MGI:101834)			
chr17	42659247	42667005	17q21	17q21.2		605785	TUBG2	"Tubulin, gamma 2"	TUBG2	27175	ENSG00000037042	pseudogene on chr. 7		Tubg2 (MGI:2144208)			
chr17	42679401	42681826	17q21.2	17q21.2		600240	"CCR10, GPR2"	Chemokine (C-C) receptor 10	CCR10	2826	ENSG00000184451			Ccr10 (MGI:1096320)			
chr17	42679766	42699992	17q21	17q21.2		602346	"CNTNAP1, CASPR, P190"	Contactin-associated protein 1	CNTNAP1	8506	ENSG00000108797		"Lethal congenital contracture syndrome 7, 616286 (3), Autosomal recessive"	Cntnap1 (MGI:1858201)			
chr17	42700274	42745095	17q21.1-q21.3	17q21.2		601674	EZH1	"Enhancer of zeste, Drosophila, homolog of, 1"	EZH1	2145	ENSG00000108799			Ezh1 (MGI:1097695)			
chr17	42761193	42763040	17q12-q21.1	17q21.2		605154	RAMP2	Receptor activity-modifying protein 2	RAMP2	10266	ENSG00000131477			Ramp2 (MGI:1859650)			
chr17	42773435	42779599	17q21.3	17q21.2		610907	"VPS25, FAP20"	"Vacuolar protein sorting 25, S. cerevisiae, homolog of"	VPS25	84313	ENSG00000131475			Vps25 (MGI:106354)			
chr17	42779700	42797065	17q21-q22	17q21.2		601844	"WNK4, PRKWNK4, PHA2B"	WNK lysine deficient protein kinase 4	WNK4	65266	ENSG00000126562		"Pseudohypoaldosteronism, type IIB, 614491 (3), Autosomal dominant"	Wnk4 (MGI:1917097)			
chr17	42797617	42798724	17q21.31	17q21.2		614775	"COA3, CCDC56"	Cytochrome c oxidase assembly factor 3	COA3	28958	ENSG00000183978			Coa3 (MGI:1098757)			
chr17	42800000	46800000	17q21.31			613533	"DUP17q21.31, C17DUPq21.31"	Chromosome 17q21.31 duplication syndrome				contiguous gene duplication syndrome	"Chromosome 17q21.31 duplication syndrome, 613533 (4)"				
chr17	42800000	52100000	17q21.3			603279	ERDA1	"Expanded repeat domain, CAG/CTG, 1"	ERDA1	9030		no apparent pathology					
chr17	42800000	59500000	17q21.31-q22			615162	MRT35	"Mental retardation, autosomal recessive 35"		101409266		between rs4792947 and rs11079258	"Mental retardation, autosomal recessive 35, 615162 (2), Autosomal recessive"				
chr17	42810131	42824315	17q21	17q21.31		604378	BECN1	Beclin 1	BECN1	8678	ENSG00000126581			Becn1 (MGI:1891828)			
chr17	42833141	42843759	17q12-q21	17q21.31		605129	"PSME3, PA28G"	Proteasome activator subunit 3	PSME3	10197	ENSG00000131467			Psme3 (MGI:1096366)			
chr17	42844582	42850711	17q21	17q21.31		602268	"AOC2, RAO"	"Amine oxidase, copper-containing, 2"	AOC2	314	ENSG00000131480			Aoc2 (MGI:2668431)			
chr17	42851181	42858129	17q21	17q21.31		603735	"AOC3, HPAO, VAP1"	"Amine oxidase, copper-containing 3"	AOC3	8639	ENSG00000131471			Aoc3 (MGI:1306797)			
chr17	42900796	42914432	17q21	17q21.31		613742	"G6PC, G6PT"	"Glucose-6-phosphatase, catalytic"	G6PC	2538	ENSG00000131482		"Glycogen storage disease Ia, 232200 (3), Autosomal recessive"	G6pc (MGI:95607)			
chr17	42950525	42964497	17q21.31	17q21.31		613212	AARSD1	Alanyl-tRNA synthetase domain-containing 1	AARSD1	80755	ENSG00000266967			Aarsd1 (MGI:1916934)			
chr17	42998272	43002958	17q21.1-q21.2	17q21.31		607526	"RPL27, DBA16"	Ribosomal protein L27	RPL27	6155	ENSG00000131469	mutation identified in 1 DBA16 patient	"?Diamond-Blackfan anemia 16, 617408 (3), Autosomal dominant"	Rpl27 (MGI:98036)			
chr17	43006724	43014458	17q21	17q21.31		600735	IFI35	Interferon-induced protein-35	IFI35	3430	ENSG00000068079			Ifi35 (MGI:1917360)			
chr17	43014604	43022441	17q21	17q21.31		604631	VAT1	Vesicle amine transport protein 1	VAT1	10493	ENSG00000108828			Vat1 (MGI:1349450)			
chr17	43025240	43032040	17q21	17q21.31		601555	"RND2, ARHN, RHO7"	"Ras homolog gene family, member N (GTP-binding protein Rho7)"	RND2	8153	ENSG00000108830			Rnd2 (MGI:1338755)			
chr17	43044294	43125482	17q21	17q21.31		113705	"BRCA1, PSCP, BROVCA1, PNCA4, FANCS"	Breast cancer-1 gene	BRCA1	672	ENSG00000012048		"{Breast-ovarian cancer, familial, 1}, 604370 (3), Autosomal dominant, Multifactorial; Fanconi anemia, complementation group S, 617883 (3), Autosomal recessive; {Pancreatic cancer, susceptibility to, 4}, 614320 (3)"	Brca1 (MGI:104537)			
chr17	43170309	43211688	17q21.1	17q21.31		166945	"NBR1, M17S2"	"Neighbor of BRCA1 gene 1 (membrane component, chromosome 17, surface marker 2)"	NBR1	4077	ENSG00000188554			Nbr1 (MGI:108498)			
chr17	43233789	43233976	17q21-q22	17q21.31		180690	"RNU2-1, RNU2"	"RNA, U2 small nuclear, 1"	RNU2-1	6066							
chr17	43398984	43401135	17q12-q21	17q21.31		600732	"ARL4D, ARF4L"	ADP-ribosylation factor-like 4D	ARL4D	379	ENSG00000175906			Arl4d (MGI:1933155)			
chr17	43483864	43544786	17q21.31	17q21.31		600396	"DHX8, DDX8, HRH1"	DEAH (Asp-Glu-Ala-His) box polypeptide 8	DHX8	1659	ENSG00000067596			Dhx8 (MGI:1306823)			
chr17	43527842	43546431	17q21	17q21.31		600711	ETV4	"ETS variant gene-4 (E1A enhancer-binding protein, E1AF)"	ETV4	2118	ENSG00000175832			Etv4 (MGI:99423)			
chr17	43640388	43661976	17q21	17q21.31		600147	"MEOX1, MOX1, KFS2"	"Mesenchyme homeo box 1 (Mox1, mouse, homolog of)"	MEOX1	4222	ENSG00000005102		"Klippel-Feil syndrome 2, 214300 (3), Autosomal recessive"	Meox1 (MGI:103220)			
chr17	43753730	43758787	17q12-q21	17q21.31		605740	"SOST, VBCH, CDD, SOST1"	Sclerostin	SOST	50964	ENSG00000167941		"Craniodiaphyseal dysplasia, autosomal dominant, 122860 (3), Autosomal dominant; Sclerosteosis 1, 269500 (3), Autosomal recessive; Van Buchem disease, 239100 (3), Autosomal recessive"	Sost (MGI:1921749)			
chr17	43766120	43778999	17q21	17q21.31		600183	"DUSP3, VHR"	Dual specificity phosphatase-3 (vaccinia virus phosphatase VH1-related)	DUSP3	1845	ENSG00000108861			Dusp3 (MGI:1919599)			
chr17	43800798	43833193	17q12-q21	17q21.31		601114	"MPP3, DLG3"	"Membrane protein, palmitoylated-3 (MAGUK p55 subfamily member 3)"	MPP3	4356	ENSG00000161647			Mpp3 (MGI:1328354)			
chr17	43847096	43863638	17q21.31	17q21.31		610520	"CD300LG, TREM4, CLM9"	"CD300 antigen-like family, member G"	CD300LG	146894	ENSG00000161649			Cd300lg (MGI:1289168)			
chr17	43875356	43909710	17q12-q21	17q21.31		600723	"MPP2, DLG2"	"Membrane protein, palmitoylated-2 (MAGUK p55 subfamily member 2)"	MPP2	4355	ENSG00000108852			Mpp2 (MGI:1858257)			
chr17	43940801	43944211	17q12-q21	17q21.31		167780	PPY	Pancreatic polypeptide	PPY	5539	ENSG00000108849	"in rat, close to GH"		Ppy (MGI:97753)			
chr17	43952732	44004468	17q21	17q21.31		600781	PYY	Peptide YY	PYY	5697	ENSG00000131096	10kb from PPY		Pyy (MGI:99924)			
chr17	44004545	44009067	17q21.31	17q21.31		608300	NAGS	N-acetylglutamate synthase	NAGS	162417	ENSG00000161653		"N-acetylglutamate synthase deficiency, 237310 (3), Autosomal recessive"	Nags (MGI:2387600)			
chr17	44034634	44067618	17q21.31	17q21.31		611793	LSM12	"LSM12, S. cerevisiae, homolog of"	LSM12	124801	ENSG00000161654			Lsm12 (MGI:1919592)			
chr17	44070699	44076343	17q21	17q21.31		611045	"G6PC3, UGRP, SCN4"	"Glucose-6-phosphatase, catalytic, 3"	G6PC3	92579	ENSG00000141349		"Dursun syndrome, 612541 (3), Autosomal recessive; Neutropenia, severe congenital 4, autosomal recessive, 612541 (3), Autosomal recessive"	G6pc3 (MGI:1915651)			
chr17	44076752	44123650	17q21	17q21.31		605315	HDAC5	Histone deacetylase 5	HDAC5	10014	ENSG00000108840			Hdac5 (MGI:1333784)			
chr17	44170705	44179082	17q21.31	17q21.31		615056	ASB16	Ankyrin repeat- and SOCS box-containing protein 16	ASB16	92591	ENSG00000161664			Asb16 (MGI:2654437)			
chr17	44205032	44221625	17q21.3	17q21.31		600673	"UBTF, UBF, CONDBA"	"Upstream binding transcription factor, RNA polymerase I"	UBTF	7343	ENSG00000108312		"Neurodegeneration, childhood-onset, with brain atrophy, 617672 (3), Autosomal dominant"	Ubtf (MGI:98512)			
chr17	44226960	44230549	17q21-q22	17q21.31		600739	SHCL1	SHC (Src homology 2 domain-containing) transforming protein-like 1	SHC1P2	6466							
chr17	44248389	44268160	17q21-q22	17q21.31		109270	"SLC4A1, AE1, EPB3, SPH4, SAO, CHC"	"Solute carrier family 4, anion exchanger, member 1 (erythrocyte membrane protein band 3, Diego blood group)"	SLC4A1	6521	ENSG00000004939		"[Blood group, Diego], 110500 (3); [Blood group, Froese], 601551 (3); [Blood group, Swann], 601550 (3); [Blood group, Waldner], 112010 (3); [Blood group, Wright], 112050 (3); Cryohydrocytosis, 185020 (3), Autosomal dominant; [Malaria, resistance to], 611162 (3); Ovalocytosis, SA type, 166900 (3), Autosomal dominant; Renal tubular acidosis, distal, AD, 179800 (3), Autosomal dominant; Renal tubular acidosis, distal, AR, 611590 (3), Autosomal recessive; Spherocytosis, type 4, 612653 (3), Autosomal dominant"	Slc4a1 (MGI:109393)			
chr17	44308558	44318669	17q21.3	17q21.31		605448	"RUNDC3A, RPIP8"	RUN domain contain 3A	RUNDC3A	10900	ENSG00000108309			Rundc3a (MGI:1858752)			
chr17	44319624	44324869	17q21.31	17q21.31		610820	"SLC25A39, CGI69"	"Solute carrier family 25, member 39"	SLC25A39	51629	ENSG00000013306			Slc25a39 (MGI:1196386)			
chr17	44345085	44353105	17q21.32	17q21.31		138945	"GRN, CLN11"	Granulin	GRN	2896	ENSG00000030582		"Aphasia, primary progressive, 607485 (3), Autosomal dominant; Ceroid lipofuscinosis, neuronal, 11, 614706 (3), Autosomal recessive; Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485 (3), Autosomal dominant"	Grn (MGI:95832)			
chr17	44372180	44389600	17q21.32	17q21.31		607759	"ITGA2B, GP2B, CD41B, GT, BDPLT2, BDPLT16"	"Integrin, alpha-2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41B)"	ITGA2B	3674	ENSG00000005961	3' to GP3A; BAK platelet antigen	"Bleeding disorder, platelet-type, 16, autosomal dominant, 187800 (3), Autosomal dominant; Glanzmann thrombasthenia, 273800 (3), Autosomal recessive; Thrombocytopenia, neonatal alloimmune, BAK antigen related (3)"	Itga2b (MGI:96601)			
chr17	44395276	44503601	17q21.31	17q21.31		614396	"GPATCH8, KIAA0553"	G-patch domain-containing protein 8	GPATCH8	23131	ENSG00000186566			Gpatch8 (MGI:1918667)			
chr17	44557443	44561261	17q21.1	17q21.31		600667	FZD2	"Frizzled, Drosophila, homolog of, 2"	FZD2	2535	ENSG00000180340			Fzd2 (MGI:1888513)			
chr17	44656393	44677085	17q21.31	17q21.31		616934	"MEIOC, C17orf104"	Meiosis-specific protein with coiled-coil domain	MEIOC	284071	ENSG00000180336			Meioc (MGI:2686410)			
chr17	44708580	44752731	17q21	17q21.31		611661	"DBF4B, DRF1, ASKL1"	"DBF4, S. cerevisiae, homolog of, B"	DBF4B	80174	ENSG00000161692						
chr17	44759150	44781845	17q21.3	17q21.31		155120	"ADAM11, MDC"	A disintegrin and metalloproteinase domain 11	ADAM11	4185	ENSG00000073670			Adam11 (MGI:1098667)			
chr17	44850286	44899624	17q21.31	17q21.31		603892	"EFTUD2, KIAA0031, MFDGA"	Elongation factor Tu GTP-binding domain-containing 2	EFTUD2	9343	ENSG00000108883		"Mandibulofacial dysostosis, Guion-Almeida type, 610536 (3), Autosomal dominant"	Eftud2 (MGI:1336880)			
chr17	44899711	44903678	17q21.31	17q21.31		614677	"CCDC103, SMH, PR46B, CILD17"	Coiled-coil domain-containing protein 103	CCDC103	388389	ENSG00000167131		"Ciliary dyskinesia, primary, 17, 614679 (3), Autosomal recessive"	Ccdc103 (MGI:1920543)			
chr17	44905625	44915551	17q21	17q21.31		137780	"GFAP, ALXDRD"	Glial fibrillary acidic protein	GFAP	2670	ENSG00000131095		"Alexander disease, 203450 (3), Autosomal dominant"	Gfap (MGI:95697)			
chr17	44924710	44947745	17q21.31	17q21.31		614570	KIF18B	Kinesin family member 18B	KIF18B	146909	ENSG00000186185			Kif18b (MGI:2446979)			
chr17	44959692	44968275	17q21	17q21.31		611586	"C1QL1, CRF, C1QRF"	"Complement component 1, q subcomponent-like 1"	C1QL1	10882	ENSG00000131094			C1ql1 (MGI:1344400)			
chr17	45061298	45109015	17q21.31	17q21.31		160993	"NMT1, NMT"	N-myristoyltransferase 1	NMT1	4836	ENSG00000136448			Nmt1 (MGI:102579)			
chr17	45147316	45152100	Chr.17	17q21.31		607328	"CLP1, HIS1"	Cardiac lineage protein 1	HEXIM1	10614	ENSG00000186834			Hexim1 (MGI:2385923)			
chr17	45159947	45170039	17q21.32	17q21.31		615695	HEXIM2	Hexamethylene bis acetamide-inducible protein 2	HEXIM2	124790	ENSG00000168517			Hexim2 (MGI:1918309)			
chr17	45220267	45247321	17q21	17q21.31		604656	"FMNL, C17orf1B"	Formin-like	FMNL1	752	ENSG00000184922						
chr17	45263118	45317063	17q21	17q21.31		604655	"MAP3K14, NIK, HSNIK"	Mitogen-activated protein kinase kinase kinase-14	MAP3K14	9020	ENSG00000006062			Map3k14 (MGI:1858204)			
chr17	45393901	45432915	17q21	17q21.31		610591	"ARHGAP27, CAMGAP1"	RHO GTPase-activating protein 27	ARHGAP27	201176	ENSG00000159314			Arhgap27 (MGI:1916903)			
chr17	45434261	45490779	17q21.3	17q21.31		611466	"PLEKHM1, AP162, KIAA0356, OPTB6"	"Pleckstrin homology domain-containing protein, family M, member 1"	PLEKHM1	9842	ENSG00000225190		"Osteopetrosis, autosomal recessive 6, 611497 (3)"	Plekhm1 (MGI:2443207)			
chr17	45784279	45835827	17q12-q22	17q21.31		122561	"CRHR1, CRHR"	Corticotropin releasing hormone receptor 1	CRHR1	1394	ENSG00000120088			Crhr1 (MGI:88498)			
chr17	45844889	45847071	17q21.31	17q21.31		608284	IMP5	Intramembrane protease 5	SPPL2C	162540	ENSG00000185294			Sppl2c (MGI:3045264)			
chr17	45894381	46028333	17q21.1	17q21.31		157140	"MAPT, MTBT1, DDPAC, MSTD"	Microtubule-associated protein tau	MAPT	4137	ENSG00000186868	see 6p21	"Dementia, frontotemporal, with or without parkinsonism, 600274 (3), Autosomal dominant; {Parkinson disease, susceptibility to}, 168600 (3), Isolated cases, Multifactorial; Pick disease, 172700 (3), Autosomal dominant, Isolated cases; Supranuclear palsy, progressive, 601104 (3), Autosomal dominant; Supranuclear palsy, progressive atypical, 260540 (3), Autosomal recessive"	Mapt (MGI:97180)			
chr17	45999249	45999693	17q21.1	17q21.31		607067	STH	Saitohin	STH	246744	ENSG00000256762	in intron 9 of TAU					
chr17	46027334	46225373	17q21.31	17q21.31		612452	"KANSL1, KIAA1267, MSL1V1, KDVS"	KAT8 regulatory NSL complex subunit 1	KANSL1	284058	ENSG00000120071		"Koolen-De Vries syndrome, 610443 (3), Autosomal dominant"	Kansl1 (MGI:1923969)			
chr17	46295130	46337793	17q21.31-q21.32	17q21.31		616555	LRRC37A	Leucine-rich repeat-containing protein 37A	LRRC37A	9884	ENSG00000176681						
chr17	46512709	47049127	17q21.31-q21.32	17q21.31-q21.32		616556	LRRC37A2	Leucine-rich repeat-containing protein 37A2	LRRC37A2	474170	ENSG00000238083						
chr17	46590668	46757463	17q21-q22	17q21.31		601633	NSF	N-ethylmaleimide-sensitive factor	NSF	4905	ENSG00000073969			Nsf (MGI:104560)			
chr17	46762505	46818759	17q21	17q21.31-q21.32		165330	"WNT3, INT4, TETAMS"	"Wingless-type MMTV integration site family, member 3"	WNT3	7473	ENSG00000108379	mutation identified in 1 TETAMS family	"?Tetra-amelia syndrome, 273395 (3), Autosomal recessive"	Wnt3 (MGI:98955)			
chr17	46833200	46886729	17q21	17q21.32		602864	WNT15	"Wingless-type MMTV integration site family, member 15"	WNT9B	7484	ENSG00000158955			Wnt9b (MGI:1197020)			
chr17	46923107	46975518	17q21	17q21.32		604027	"GOSR2, GS27, EPM6"	Golgi snap receptor complex member 2	GOSR2	9570	ENSG00000108433		"Epilepsy, progressive myoclonic 6, 614018 (3), Autosomal recessive"	Gosr2 (MGI:1927204)			
chr17	47117696	47189338	17q12-q23.2	17q21.32		116946	CDC27	Cell division cycle 27	CDC27	996	ENSG00000004897	between ERBB2 and PRKCA		Cdc27 (MGI:102685)			
chr17	47209016	47227649	17q21.32	17q21.32		160770	MYL4	"Myosin, light polypeptide-4, alkali, atrial, embryonic"	MYL4	4635	ENSG00000198336	mutation identified in 1 ATFB18 family	"?Atrial fibrillation, familial, 18, 617280 (3), Autosomal dominant"	Myl4 (MGI:97267)			
chr17	47253841	47312710	17q21.32	17q21.32		173470	"ITGB3, GP3A, GT, BDPLT2, BDPLT16"	"Integrin, beta-3 (platelet glycoprotein IIIa; antigen CD61)"	ITGB3	3690	ENSG00000259207	in same 260kb fragment as GP2B; PL(A) platelet antigen	"Bleeding disorder, platelet-type, 16, autosomal dominant, 187800 (3), Autosomal dominant; Glanzmann thrombasthenia, 273800 (3), Autosomal recessive; {Myocardial infarction, susceptibility to}, 608446 (3); Purpura, posttransfusion (3); Thrombocytopenia, neonatal alloimmune (3)"	Itgb3 (MGI:96612)			
chr17	47522949	47623275	17q21	17q21.32		606793	"NPEPPS, PSA, MP100"	"Aminopeptidase, puromycin-sensitive"	NPEPPS	9520	ENSG00000141279			Npepps (MGI:1101358)			
chr17	47649837	47683637	17q21	17q21.32		602738	KPNB1	Karyopherin beta-1	KPNB1	3837	ENSG00000108424			Kpnb1 (MGI:107532)			
chr17	47694064	47712062	17q21.32	17q21.32		608476	"TBKBP1, PROSAPIP2, KIAA0775"	TBK1-binding protein 1	TBKBP1	9755	ENSG00000198933			Tbkbp1 (MGI:1920424)			
chr17	47733243	47746118	17q21.3	17q21.32		604895	"TBX21, TBET"	T-box 21	TBX21	30009	ENSG00000073861		"Asthma and nasal polyps, 208550 (3), Autosomal recessive; {Asthma, aspirin-induced, susceptibility to}, 208550 (3), Autosomal recessive"	Tbx21 (MGI:1888984)			
chr17	47807366	47821821	17q21.2	17q21.32		606735	"OSBPL7, ORP7"	Oxysterol-binding protein-like protein 7	OSBPL7	114881	ENSG00000006025			Osbpl7 (MGI:1918490)			
chr17	47823271	47831540	17q21.3	17q21.32		611825	"MRPL10, MRPL8"	Mitochondrial ribosomal protein L10	MRPL10	124995	ENSG00000159111			Mrpl10 (MGI:1333801)			
chr17	47837680	47841332	17q21.3	17q21.32		614966	"SCRN2, SES2"	Secernin 2	SCRN2	90507	ENSG00000141295			Scrn2 (MGI:1343092)			
chr17	47896031	47932270	17q21.32	17q21.32		601801	SP2	Transcription factor Sp2	SP2	6668	ENSG00000167182			Sp2 (MGI:1926162)			
chr17	47941522	47949307	17q21.32	17q21.32		603287	PNPO	Pyridoxamine 5'-phosphate oxidase	PNPO	55163	ENSG00000108439		"Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3), Autosomal recessive"	Pnpo (MGI:2144151)			
chr17	47967903	47981785	17q21.31	17q21.32		608202	CDK5RAP3	CDK5 regulatory subunit-associated protein 3	CDK5RAP3	80279	ENSG00000108465			Cdk5rap3 (MGI:1933126)			
chr17	48026166	48048085	17q21.32	17q21.32		615526	COPZ2	"Coatomer protein complex, subunit zeta-2"	COPZ2	51226	ENSG00000005243			Copz2 (MGI:1929008)			
chr17	48037160	48037246	17q21.32	17q21.32		613788	"MIR152, MIRN152"	Micro RNA 152	MIR152	406943							
chr17	48048304	48061544	17q21.3	17q21.32		163260	"NFE2L1, NRF1"	"Nuclear factor, erythroid-derived 2-like 1"	NFE2L1	4779	ENSG00000082641			Nfe2l1 (MGI:99421)			
chr17	48107532	48123600	17q21.32	17q21.32		614906	SNX11	Sorting nexin 11	SNX11	29916	ENSG00000002919			Snx11 (MGI:1921729)			
chr17	48133437	48430249	17q21.32	17q21.32		604969	"SKAP1, SCAP1, SKAP55"	"SRC kinase-associated phosphoprotein 1, 55kD"	SKAP1	8631	ENSG00000141293			Skap1 (MGI:1925723)			
chr17	48529444	48530909	17q21-q22	17q21.32		142968	"HOXB1, HOX2I, HCFP3"	Homeo box-B1	HOXB1	3211	ENSG00000120094		"Facial paresis, hereditary congenital, 3, 614744 (3), Autosomal recessive"	Hoxb1 (MGI:96182)			
chr17	48542654	48545030	17q21-q22	17q21.32		142967	"HOXB2, HOX2H"	Homeo box-B2	HOXB2	3212	ENSG00000173917			Hoxb2 (MGI:96183)			
chr17	48548869	48590271	17q21-q22	17q21.32		142966	"HOXB3, HOX2G"	Homeo box-B3	HOXB3	3213	ENSG00000120093			Hoxb3 (MGI:96184)			
chr17	48575506	48578380	17q21-q22	17q21.32		142965	"HOXB4, HOX2F"	Homeo box-B4	HOXB4	3214	ENSG00000182742			Hoxb4 (MGI:96185)			
chr17	48579837	48579946	17q21	17q21.32		610173	MIR10A	Micro RNA 10A	MIR10A	406902							
chr17	48591256	48593740	17q21-q22	17q21.32		142960	"HOXB5, HOX2A"	Homeo box-B5	HOXB5	3215	ENSG00000120075			Hoxb5 (MGI:96186)			
chr17	48595735	48604991	17q21-q22	17q21.32		142961	"HOXB6, HOX2B"	Homeo box-B6	HOXB6	3216	ENSG00000108511			Hoxb6 (MGI:96187)			
chr17	48607231	48611020	17q21-q22	17q21.32		142962	"HOXB7, HOX2C"	Homeo box-B7	HOXB7	3217	ENSG00000260027			Hoxb7 (MGI:96188)			
chr17	48612345	48619530	17q21-q22	17q21.32		142963	"HOXB8, HOX2D"	Homeo box-B8	HOXB8	3218	ENSG00000120068			Hoxb8 (MGI:96189)			
chr17	48621155	48626472	17q21-q22	17q21.32		142964	"HOXB9, HOX2E"	Homeo box-B9	HOXB9	3219	ENSG00000170689			Hoxb9 (MGI:96190)			
chr17	48632489	48632558	17q21-q22	17q21.32		608632	"MIR196A1, MIRN196A1"	Micro RNA 196A1	MIR196A1	406972							
chr17	48720801	48724757	17q21.3	17q21.32		610787	"HOXBAS5, PRAC2"	HOXB cluster antisense RNA 5	PRAC2	360205	ENSG00000229637						
chr17	48721718	48722519	17q21.3	17q21.32		609819	PRAC1	"Prostate, rectum, and colon gene"	PRAC1	84366	ENSG00000159182						
chr17	48724762	48728748	17q21.2	17q21.32		604607	HOXB13	Homeo box B13	HOXB13	10481	ENSG00000159184			Hoxb13 (MGI:107730)			
chr17	48762230	48817246	17q21.32	17q21.32		610849	TTLL6	"Tubulin tyrosine ligase-like family, member 6"	TTLL6	284076	ENSG00000170703			Ttll6 (MGI:2683461)			
chr17	48892785	48895870	Chr.17	17q21.32		603192	ATP5G1	"ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C, isoform 1"	ATP5MC1	516	ENSG00000159199			Atp5g1 (MGI:107653)			
chr17	48908368	48929059	17q21.32	17q21.32		611362	"UBE2Z, USE1"	Ubiquitin-conjugating enzyme E2Z	UBE2Z	65264	ENSG00000159202			Ube2z (MGI:1343160)			
chr17	48930095	48944841	17q21.32	17q21.32		610904	"SNF8, VPS22, EAP30"	"SNF8, S. cerevisiae, homolog of"	SNF8	11267	ENSG00000159210			Snf8 (MGI:1343161)			
chr17	48958555	48968592	17q21.3-q22	17q21.32		137240	GIP	Gastric inhibitory polypeptide	GIP	2695	ENSG00000159224			Gip (MGI:107504)			
chr17	48997411	49056144	17q21.3	17q21.32		608288	"IGF2BP1, IMP1, CRDBP, ZBP1"	Insulin-like growth factor 2 mRNA-binding protein 1	IGF2BP1	10642	ENSG00000159217			Igf2bp1 (MGI:1890357)			
chr17	49120346	49170721	17q21.2	17q21.32		111730	"B4GALGT2, GALGT2, SD"	"Beta-1,4-N-acetyl-galactosaminyl transferase 2"	B4GALNT2	124872	ENSG00000167080			B4galnt2 (MGI:1342058)			
chr17	49206233	49210573	17q21	17q21.32		139391	GNGT2	"Guanine nucleotide-binding protein, gamma-transducing activity polypeptide 2"	GNGT2	2793	ENSG00000167083			Gngt2 (MGI:893584)			
chr17	49210226	49223224	17q21.3	17q21.32		606363	NESH	NESH protein	ABI3	51225	ENSG00000108798			Abi3 (MGI:1913860)			
chr17	49289205	49362472	17q21.32	17q21.32-q21.33		613907	"ZNF652, KIAA0924"	Zinc finger protein 652	ZNF652	22834	ENSG00000198740			Zfp652 (MGI:2442221)			
chr17	49404047	49414904	17q21	17q21.33		176705	PHB	Prohibitin	PHB	5245	ENSG00000167085		"{Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant"	Phb (MGI:97572)			
chr17	49495292	49515019	17q21-q22	17q21.33		162010	"NGFR, TNFRSF16"	Nerve growth factor receptor	NGFR	4804	ENSG00000064300	"distal to APL breakpoint, q21; < 0.5mb from HOX2"		Ngfr (MGI:97323)			
chr17	49575935	49583809	17q21.33	17q21.33		604636	"NXPH3, NPH3"	Neuroexophilin 3	NXPH3	11248	ENSG00000182575			Nxph3 (MGI:1336188)			
chr17	49598883	49678162	17q21.33	17q21.33		602650	SPOP	Speckle-type POZ protein	SPOP	8405	ENSG00000121067			Spop (MGI:1343085)			
chr17	49700933	49708172	17q21.33	17q21.33		610790	"SLC35B1, UGTREL1"	"Solute carrier family 35, member B1"	SLC35B1	10237	ENSG00000121073			Slc35b1 (MGI:1343133)			
chr17	49788618	49829095	17q21.32	17q21.33		609880	"KAT7, MYST2, HBO1"	K(lysine) acetyltransferase 7	KAT7	11143	ENSG00000136504			Kat7 (MGI:2182799)			
chr17	49838308	49848016	17q21.3	17q21.33		607833	"RAC4, PPTC, HK1"	Tachykinin 4	TAC4	255061	ENSG00000176358						
chr17	49968969	49974958	17q21.3-q22	17q21.33		601911	"DLX4, DLX7, DLX8, OFC15"	Distal-less homeo box-4	DLX4	1748	ENSG00000108813	mutation identified in 1 OFC15 family	"?Orofacial cleft 15, 616788 (3), Autosomal dominant"	Dlx4 (MGI:94904)			
chr17	49990004	49995223	17q21.3-q22	17q21.33		600525	"DLX3, TDO, AI4"	Distal-less homeo box-3	DLX3	1747	ENSG00000064195		"Amelogenesis imperfecta, type IV, 104510 (3), Autosomal dominant; Trichodontoosseous syndrome, 190320 (3), Autosomal dominant"	Dlx3 (MGI:94903)			
chr17	50055967	50090484	17q21.33	17q21.33		605025	"ITGA3, CD49C, GAPB3, ILNEB"	"Integrin, alpha-3"	ITGA3	3675	ENSG00000005884		"Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital, 614748 (3), Autosomal recessive"	Itga3 (MGI:96602)			
chr17	50094736	50111368	17q21.33	17q21.33		602525	PDK2	"Pyruvate dehydrogenase kinase, isoenzyme 2"	PDK2	5164	ENSG00000005882			Pdk2 (MGI:1343087)			
chr17	50133734	50151026	17q21.33	17q21.33		603325	"PPP1R9B, SPINO"	"Protein phosphatase 1, regulatory subunit 9B"	PPP1R9B	84687	ENSG00000108819			Ppp1r9b (MGI:2387581)			
chr17	50165516	50175931	17q12-q21.33	17q21.33		600119	"SGCA, ADL, DAG2, LGMD2D, DMDA2"	"Sarcoglycan, alpha (50kD dystrophin-associated glycoprotein; adhalin)"	SGCA	6442	ENSG00000108823		"Muscular dystrophy, limb-girdle, type 2D, 608099 (3), Autosomal recessive"	Sgca (MGI:894698)			
chr17	50171427	50172475	17q21.33	17q21.33		608101	HILS1	Spermatid-specific linker histone H1-like protein	HILS1	373861							
chr17	50184095	50201648	17q21.31-q22	17q21.33		120150	"COL1A1, OI1, OI2, OI3, OI4, EDSARTH1"	"Collagen I, alpha-1 polypeptide"	COL1A1	1277	ENSG00000108821	fused with PDGFB in DFPB	"{Bone mineral density variation QTL, osteoporosis}, 166710 (3), Autosomal dominant; Caffey disease, 114000 (3), Autosomal dominant; Ehlers-Danlos syndrome, arthrochalasia type, 1, 130060 (3), Autosomal dominant; Osteogenesis imperfecta, type I, 166200 (3), Autosomal dominant; Osteogenesis imperfecta, type II, 166210 (3), Autosomal dominant; Osteogenesis imperfecta, type III, 259420 (3), Autosomal dominant; Osteogenesis imperfecta, type IV, 166220 (3), Autosomal dominant"	Col1a1 (MGI:88467)			
chr17	50346031	50361184	17q21.3-q22	17q21.33		608125	"XYLT2, XT2, SOS"	Xylosyltransferase 2	XYLT2	64132	ENSG00000015532		"{Pseudoxanthoma elasticum, modifier of severity of}, 264800 (3), Autosomal recessive; Spondyloocular syndrome, 605822 (3), Autosomal recessive"	Xylt2 (MGI:2444797)			
chr17	50367866	50373200	17q21.3-q22	17q21.33		611837	MRPL27	Mitochondrial ribosomal protein L27	MRPL27	51264	ENSG00000108826			Mrpl27 (MGI:2137224)			
chr17	50373219	50381478	17q21.3	17q21.33		610885	EME1	"Essential meiotic endonuclease 1, S. pombe, homolog of, 1"	EME1	146956	ENSG00000154920			Eme1 (MGI:3576783)			
chr17	50381232	50397552	17q21.33	17q21.33		614854	"LRRC59, p34"	Leucine-rich repeat-containing protein 59	LRRC59	55379	ENSG00000108829			Lrrc59 (MGI:2138133)			
chr17	50426157	50474844	17q21.33	17q21.33		610465	"ACSF2, FLJ20920"	Acyl-CoA synthetase family member 2	ACSF2	80221	ENSG00000167107			Acsf2 (MGI:2388287)			
chr17	50464491	50469880	17q21.33	17q21.33		602178	CHAD	Chondroadherin	CHAD	1101	ENSG00000136457			Chad (MGI:1096866)			
chr17	50507777	50531501	17q21	17q21.33		609835	"MYCBPAP, AMAP1"	MYCBP-associated protein	MYCBPAP	84073	ENSG00000136449			Mycbpap (MGI:2388726)			
chr17	50532686	50543749	Chr.17	17q21.33		607264	EPN3	Epsin 3	EPN3	55040	ENSG00000049283			Epn3 (MGI:1919139)			
chr17	50547088	50555851	17q21.33	17q21.33		613939	"SPATA20, SSP411"	Spermatogenesis-associated protein 20	SPATA20	64847	ENSG00000006282			Spata20 (MGI:2183449)			
chr17	50560932	50629624	17q22	17q21.33		604065	"CACNA1G, SCA42"	"Calcium channel, voltage-dependent, T type, alpha-1G subunit"	CACNA1G	8913	ENSG00000006283		"Spinocerebellar ataxia 42, 616795 (3), Autosomal dominant"	Cacna1g (MGI:1201678)			
chr17	50634842	50691703	17q22	17q21.33		604323	"ABCC3, CMOAT2, MRP3, MLP2"	"ATP-binding cassette, sub-family C, member 3"	ABCC3	8714	ENSG00000108846			Abcc3 (MGI:1923658)			
chr17	50719543	50756212	17q21.3	17q21.33		609434	"LUC7L3, CROP, LUC7A"	"Luc7, S. cerevisiae, homolog of, 3"	LUC7L3	51747	ENSG00000108848			Luc7l3 (MGI:1914934)			
chr17	50834649	50842352	17q21.3	17q21.33		610895	"WFIKKN2, WFIKKNRP"	"WAP, fillistatin, immunoglobulin, Kunitz, and NTR domains-containing protein 2"	WFIKKN2	124857	ENSG00000173714			Wfikkn2 (MGI:2669209)			
chr17	50862222	50867977	17q21	17q21.33		605523	"TOB1, TOB"	"Transducer of ERBB2, 1"	TOB1	10140	ENSG00000141232			Tob1 (MGI:1349721)			
chr17	50962173	51120864	17q21.33	17q21.33		605430	"SPAG9, SYD1, KIAA0516"	Sperm-associated antigen 9	SPAG9	9043	ENSG00000008294			Spag9 (MGI:1918084)			
chr17	51153558	51162088	17q21.3	17q21.33		156490	"NME1, NM23"	"Non-metastatic cells 1, protein (NM23A) expressed in"	NME1	4830	ENSG00000239672		"Neuroblastoma, 256700 (3), Autosomal dominant, Isolated cases"	Nme1 (MGI:97355)			
chr17	51165434	51171743	17q21.3	17q21.33		156491	NME2	"Non-metastatic cells 2, protein (NM23) expressed in"	NME2	4831	ENSG00000243678			Nme2 (MGI:97356)			
chr17	51260535	51297932	17q21.33	17q21.33		612816	UTP18	"UTP18, S. cerevisiae, homolog of"	UTP18	51096	ENSG00000011260			Utp18 (MGI:1923402)			
chr17	51630312	52160016	17q21.33-q22	17q21-q22		604642	"CA10, CARPX"	Carbonic anhydrase X	CA10	56934	ENSG00000154975			Car10 (MGI:1919855)			
chr17	52100000	59500000	17q22			151441	BCL5	B-cell CLL/lymphoma-5	BCL5	603							
chr17	53822877	53825211	17q22	17q22		615142	KIF2B	Kinesin family member 2B	KIF2B	84643	ENSG00000141200			Kif2b (MGI:1920720)			
chr17	54900690	54961966	17q22	17q22		604701	TOM1L1	TOM1-like 1	TOM1L1	10040	ENSG00000141198			Tom1l1 (MGI:1919193)			
chr17	54951897	54968784	17q22	17q22		603648	COX11	"Cytochrome c oxidase, subunit 11"	COX11	1353	ENSG00000166260	pseudogene on 6p23-p22		Cox11 (MGI:1917052)			
chr17	54968727	55164284	17q22	17q22		610415	"STXBP4, SYNIP"	Syntaxin-binding protein 4	STXBP4	252983	ENSG00000166263			Stxbp4 (MGI:1342296)			
chr17	55264959	55325175	17q22	17q22		142385	HLF	Hepatic leukemia factor	HLF	3131	ENSG00000108924			Hlf (MGI:96108)			
chr17	55392612	55421979	17q22	17q22		604467	"MMD, MMD1, PAQR11"	Monocyte-to-macrophage differentiation-associated protein	MMD	23531	ENSG00000108960			Mmd (MGI:1914718)			
chr17	55719626	55732120	17q22	17q22		616334	TMEM100	Transmembrane protein 100	TMEM100	55273	ENSG00000166292			Tmem100 (MGI:1915138)			
chr17	55750978	55845000	17q21-q22	17q22		606055	PCTP	Phosphatidylcholine transfer protein	PCTP	58488	ENSG00000141179			Pctp (MGI:107375)			
chr17	56593698	56595589	17q22	17q22		602991	"NOG, SYM1, SYNS1A"	"Noggin, mouse, homolog of"	NOG	9241	ENSG00000183691		"Brachydactyly, type B2, 611377 (3), Autosomal dominant; Multiple synostoses syndrome 1, 186500 (3), Autosomal dominant; Stapes ankylosis with broad thumbs and toes, 184460 (3), Autosomal dominant; Symphalangism, proximal, 1A, 185800 (3), Autosomal dominant; Tarsal-carpal coalition syndrome, 186570 (3), Autosomal dominant"	Nog (MGI:104327)			
chr17	56834098	56869566	17q22	17q22		601440	"DGKE, NPHS7, AHUS7"	"Diacylglycerol kinase, epsilon, 64-kD"	DGKE	8526	ENSG00000153933		"{Hemolytic uremic syndrome, atypical, susceptibility to, 7}, 615008 (3), Autosomal recessive; Nephrotic syndrome, type 7, 615008 (3), Autosomal recessive"	Dgke (MGI:1889276)			
chr17	56887908	56914047	17q23.1	17q22		600453	"TRIM25, ZNF147, EFP"	Tripartite motif-containing 25	TRIM25	7706	ENSG00000121060	300kb from MPO		Trim25 (MGI:102749)			
chr17	56938198	56961049	17q22-q23	17q22		600272	"COIL, CLN80"	Coilin p80	COIL	8161	ENSG00000121058			Coil (MGI:104842)			
chr17	57085191	57121348	Chr.17	17q22		602449	"AKAP1, AKAP149, SAKAP84"	"A-kinase anchor protein 1, 149kD"	AKAP1	8165	ENSG00000121057			Akap1 (MGI:104729)			
chr17	57255850	57684688	17q22	17q22		607897	MSI2	"Musashi, Drosophila, homolog of, 2"	MSI2	124540	ENSG00000153944			Msi2 (MGI:1923876)			
chr17	57838925	57850071	17q22-q23	17q22		611985	MRPS23	Mitochondrial ribosomal protein S23	MRPS23	51649	ENSG00000181610			Mrps23 (MGI:1928138)			
chr17	57971546	57988263	17q22	17q22		606747	"VEZF1, ZNF161"	Vascular endothelial zinc finger 1	VEZF1	7716	ENSG00000136451			Vezf1 (MGI:1313291)			
chr17	58000918	58007345	17q21.3-q22	17q22		600812	"SRSF1, SFRS1, ASF, SF2, SRp30a"	"Splicing factor, arginine/serine-rich 1 (splicing factor 2, alternate splicing factor)"	SRSF1	6426	ENSG00000136450			Srsf1 (MGI:98283)			
chr17	58083418	58090256	17q23.2	17q22		608942	"DYNLL2, DLC2"	"Dynein, light chain, LC8-type 2"	DYNLL2	140735	ENSG00000264364			Dynll2 (MGI:1915347)			
chr17	58192723	58205173	17q23.1	17q22		131399	"EPX, EPXD"	Eosinophil peroxidase	EPX	8288	ENSG00000121053		"[Eosinophil peroxidase deficiency], 261500 (3), Autosomal recessive"	Epx (MGI:107569)			
chr17	58205435	58219604	17q23	17q22		609883	"MKS1, MKS, BBS13, JBTS28"	MKS1 gene	MKS1	54903	ENSG00000011143	frequent in Finland	"Bardet-Biedl syndrome 13, 615990 (3), Autosomal recessive; Joubert syndrome 28, 617121 (3), Autosomal recessive; Meckel syndrome 1, 249000 (3), Autosomal recessive"	Mks1 (MGI:3584243)			
chr17	58238425	58268517	17q23.1	17q22		150205	LPO	Lactoperoxidase	LPO	4025	ENSG00000167419			Lpo (MGI:1923363)			
chr17	58269855	58280934	17q23.1	17q22		606989	MPO	Myeloperoxidase	MPO	4353	ENSG00000005381	translocated in t(15;17)(q22;q11.2)	"{Alzheimer disease, susceptibility to}, 104300 (3), Autosomal dominant; {Lung cancer, protection against, in smokers} (3); Myeloperoxidase deficiency, 254600 (3), Autosomal recessive"	Mpo (MGI:97137)			
chr17	58301226	58329029	17q23.2	17q22		610764	"BZRAP1, PRAX1, RIMBP1, KIAA0612"	Benzodiazapine receptor (peripheral)-associated protein 1	TSPOAP1	9256	ENSG00000005379			Tspoap1 (MGI:2450877)			
chr17	58331231	58331317	17q22	17q22		615657	MIR142	Micro RNA 142	MIR142	406934							
chr17	58352499	58418893	17q23.2	17q22		612482	"RNF43, RNF124, SSPCS"	Ring finger protein 43	RNF43	54894	ENSG00000108375		"Sessile serrated polyposis cancer syndrome, 617108 (3), Autosomal dominant"	Rnf43 (MGI:2442609)			
chr17	58489531	58518108	Chr.17	17q22		603559	MTMR4	Myotubularin-related protein 4	MTMR4	9110	ENSG00000108389			Mtmr4 (MGI:2180699)			
chr17	58520249	58540817	17q23	17q22		603696	"SEPT4, PNUTL2"	Septin 4	4-Sep	5414	ENSG00000108387			Sept4 (MGI:1270156)			
chr17	58556676	58692054	17q22	17q22		605792	"TEX14, SPGF23"	Testis-expressed gene 14	TEX14	56155	ENSG00000121101	mutation identified in 1 SPGF23 family	"?Spermatogenic failure 23, 617707 (3), Autosomal recessive"	Tex14 (MGI:1933227)			
chr17	58692139	58734341	17q22	17q22		602774	"RAD51C, FANCO, BROVCA3"	"RAD51, S. cerevisiae, homolog of, C"	RAD51C	5889	ENSG00000108384		"{Breast-ovarian cancer, familial, susceptibility to, 3}, 613399 (3); Fanconi anemia, complementation group O, 613390 (3), Autosomal recessive"	Rad51c (MGI:2150020)			
chr17	58968009	59106963	17q22-q23	17q22		605073	"TRIM37, MUL, KIAA0898"	Tripartite motif-containing 37	TRIM37	4591	ENSG00000108395		"Mulibrey nanism, 253250 (3), Autosomal recessive"	Trim37 (MGI:2153072)			
chr17	59109858	59155438	17q22	17q22		616674	"SKA2, FAM33A"	"Spindle- and kinetochore-associated complex, subunit 2"	SKA2	348235	ENSG00000182628			Ska2 (MGI:1913390)			
chr17	59151135	59151220	17q22	17q22		615675	"MIR301A, MIR301"	Micro RNA 301A	MIR301A	407027							
chr17	59155354	59206708	17q22	17q22		615920	PRR11	Proline-rich protein 11	PRR11	55771	ENSG00000068489			Prr11 (MGI:2444496)			
chr17	59210009	59215249	17q22	17q22		613175	"C17orf71, SMG8"	Chromosome 17 open reading frame 71	SMG8	55181	ENSG00000167447			Smg8 (MGI:1921383)			
chr17	59220466	59275969	17q23.2	17q22		616317	"GDPD1, GDE4"	Glycerophosphodiester phosphodiesterase domain-containing protein 1	GDPD1	284161	ENSG00000153982			Gdpd1 (MGI:1913819)			
chr17	59331691	59401733	17q23.2	17q22		609723	YPEL2	Yippee-like 2	YPEL2	388403	ENSG00000175155			Ypel2 (MGI:1925114)			
chr17	59500000	64600000	17q23			609656	BSZQTL	Bone size quantitative trait locus 1		100188793			"{Bone size QTL}, 609656 (2)"				
chr17	59500000	63100000	17q23.1-q23.2			613355	"DEL17q23.1q23.2, C17DELq23.1q23.2"	Chromosome 17q23.1-q23.2 deletion syndrome					"Chromosome 17q23.1-q23.2 deletion syndrome, 613355 (4), Isolated cases"				
chr17	59500000	63100000	17q23.1-q23.2			613618	"DUP17q23.1q23.2, C17DUPq23.1q23.2"	Chromosome 17q23.1-q23.2 duplication syndrome				2.2 Mb contiguous gene duplication syndrome	"Chromosome 17q23.1-q23.2 duplication syndrome, 613618 (4), Autosomal dominant"				
chr17	59500000	83257441	17q23-qter			170200	PEPE	Peptidase E	PEPE	5185							
chr17	59565524	59608351	17q23.3	17q23.1		607570	"DHX40, DDX40"	DEAH (Asp-Glu-Ala-His) box polypeptide 40	DHX40	79665	ENSG00000108406			Dhx40 (MGI:1914737)			
chr17	59619688	59696955	17q23	17q23.1		118955	"CLTC, MRD56"	"Clathrin, heavy polypeptide (Hc)"	CLTC	1213	ENSG00000141367	fusion gene with TFE3 in renal adenocarcinoma	"Mental retardation, autosomal dominant 56, 617854 (3)"	Cltc (MGI:2388633)			
chr17	59697305	59707625	17q23.1	17q23.1		608625	"PTRH2, BIT1, IMNEPD"	Peptidyl-tRNA hydrolase 2	PTRH2	51651	ENSG00000141378		"Infantile-onset multisystem neurologic, endocrine, and pancreatic disease, 616263 (3), Autosomal recessive"	Ptrh2 (MGI:2444848)			
chr17	59707464	59842254	17q23.1	17q23.1		611753	"VMP1, TMEM49, EPG3"	Vacuole membrane protein 1	VMP1	81671	ENSG00000062716			Vmp1 (MGI:1923159)			
chr17	59841265	59841336	17q23.1	17q23.1		611020	"MIR21, MIRN21"	Micro RNA 21	MIR21	406991							
chr17	59859466	59892947	Chr.17	17q23.1		607344	"TUBD1, TUBD"	"Tubulin, delta-1"	TUBD1	51174	ENSG00000108423			Tubd1 (MGI:1891826)			
chr17	59893045	59950425	17q23.1	17q23.1		608938	"RPS6KB1, S6K1"	"Ribosomal protein S6 kinase, 70kD"	RPS6KB1	6198	ENSG00000108443			Rps6kb1 (MGI:1270849)			
chr17	59952361	59964755	17q23.1	17q23.1		615172	RNFT1	"RING finger protein, transmembrane 1"	RNFT1	51136	ENSG00000189050			Rnft1 (MGI:1924142)			
chr17	60083565	60088466	17q23	17q23.1		615772	"LNCDC, LOC615638"	"Long noncoding RNA, dendritic cell"	WFDC21P	645638							
chr17	60149935	60179020	17q23	17q23.1		114760	"CA4, RP17"	Carbonic anhydrase IV	CA4	762	ENSG00000167434		"Retinitis pigmentosa 17, 600852 (3), Autosomal dominant"	Car4 (MGI:1096574)			
chr17	60177230	60422469	17q22	17q23.1-q23.2		607740	"USP32, USP10"	Ubiquitin-specific protease 32	USP32	84669	ENSG00000170832			Usp32 (MGI:2144475)			
chr17	60200000	76800000	17q23.2-q25.1			612967	BMIQ15	Body mass index quantitative trait locus 15		100302719		associated with rs228883 and rs1005651	"[Body mass index QTL 15], 612967 (2)"				
chr17	60443148	60526239	17q22-q23	17q23.2		605324	"APPBP2, PAT1"	Amyloid beta precursor protein-binding protein 2	APPBP2	10513	ENSG00000062725			Appbp2 (MGI:1914134)			
chr17	60600182	60666279	17q22-q23	17q23.2		605100	"PPM1D, WIP1, IDDGIP"	"Protein phosphatase, magnesium-dependent, 1, delta isoform"	PPM1D	8493	ENSG00000170836	amplified in breast cancer	"Breast cancer, somatic, 114480 (3); Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold, 617450 (3), Autosomal dominant"	Ppm1d (MGI:1858214)			
chr17	61399895	61409465	17q23	17q23.2		600747	TBX2	T-box 2	TBX2	6909	ENSG00000121068			Tbx2 (MGI:98494)			
chr17	61452417	61485109	17q21-q22	17q23.2		601719	"TBX4, ICPPS"	T-box 4	TBX4	9496	ENSG00000121075		"Ischiocoxopodopatellar syndrome, 147891 (3), Autosomal dominant"	Tbx4 (MGI:102556)			
chr17	61679185	61864119	17q22	17q23.2		605882	"BRIP1, BACH1, FANCJ"	BRCA1-associated C-terminal helicase 1	BRIP1	83990	ENSG00000136492	?or 17q23	"Breast cancer, early-onset, 114480 (3), Autosomal dominant; Fanconi anemia, complementation group J, 609054 (3)"	Brip1 (MGI:2442836)			
chr17	61865366	61928031	17q23.2	17q23.2		611346	"INTS2, INT2, KIAA1287"	Integrator complex subunit 2	INTS2	57508	ENSG00000108506			Ints2 (MGI:1917672)			
chr17	61942604	62065982	17q22-q23	17q23.2		603808	"MED13, THRAP1, TRAP240"	Mediator complex subunit 13	MED13	9969	ENSG00000108510			Med13 (MGI:3029632)			
chr17	62470907	62615480	17q23.2	17q23.2		608439	TLK2	Tousled-like kinase 2	TLK2	11011	ENSG00000146872			Tlk2 (MGI:1346023)			
chr17	62627400	62693600	17q23.2	17q23.2		612264	"MRC2, ENDO180, UPARAP, CD280"	"Mannose receptor, C-type, 2"	MRC2	9902	ENSG00000011028			Mrc2 (MGI:107818)			
chr17	62701313	62808380	17q23.2	17q23.2		613337	10-Mar	Membrane-associated RING-CH finger protein 10	10-Mar	162333	ENSG00000173838			March10 (MGI:2443469)			
chr17	62966522	63427705	17q23.3	17q23.2-q23.3		615047	"TANC2, KIAA1636"	"Tetratricopeptide repeat-, ankyrin repeat-, and coiled-coil-containing protein 2"	TANC2	26115	ENSG00000170921			Tanc2 (MGI:2444121)			
chr17	63432302	63446360	17q11-qter	17q23.3		600019	CYB561	Cytochrome b-561	CYB561	1534	ENSG00000008283			Cyb561 (MGI:103253)			
chr17	63477060	63498379	17q23	17q23.3		106180	"ACE, DCP1, ACE1, MVCD3, ICH"	Angiotensin I converting enzyme (dipeptidyl carboxypeptidase-1)	ACE	1636	ENSG00000159640		"[Angiotensin I-converting enzyme, benign serum increase] (3); {Microvascular complications of diabetes 3}, 612624 (3); {Myocardial infarction, susceptibility to} (3); Renal tubular dysgenesis, 267430 (3), Autosomal recessive; {SARS, progression of} (3); {Stroke, hemorrhagic}, 614519 (3)"	Ace (MGI:87874)			
chr17	63523333	63548976	17q23.3	17q23.3		608168	"KCNH6, HERG2"	"Potassium channel, voltage-gated, subfamily H, member 6"	KCNH6	81033	ENSG00000173826			Kcnh6 (MGI:2684139)			
chr17	63600871	63608364	17q22-q24.2	17q23.3		612958	"TACO1, CCDC44"	Translational activator of mitochondrially encoded cytochrome c oxidase subunit I	TACO1	51204	ENSG00000136463		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Taco1 (MGI:1917457)			
chr17	63622208	63696309	17q23.3	17q23.3		602539	"MAP3K3, MEKK3, MAPKKK3"	Mitogen-activated kinase kinase kinase 3	MAP3K3	4215	ENSG00000198909			Map3k3 (MGI:1346874)			
chr17	63702831	63741969	17q23.3	17q23.3		608626	"STRADA, STRAD, LYK5"	STE20-related kinase adaptor alpha	STRADA	92335	ENSG00000266173		"Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087 (3), Autosomal recessive"	Strada (MGI:1919399)			
chr17	63773855	63819316	17q23.3	17q23.3		613369	"DDX42, RHELP"	DEAD (Asp-Glu-Ala-Asp) box polypeptide 42	DDX42	11325	ENSG00000198231			Ddx42 (MGI:1919297)			
chr17	63827409	63832026	17q24-q25	17q23.3		601681	"PSMC5, TRIP1"	"Proteasome (prosome, macropain) 26S subunit, ATPase, 5"	PSMC5	5705	ENSG00000087191			Psmc5 (MGI:105047)			
chr17	63832080	63842990	17q23-q24	17q23.3		601736	"SMARCD2, BAF60B, SGD2"	"SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily d, member 2"	SMARCD2	6603	ENSG00000108604		"Specific granule deficiency 2, 617475 (3), Autosomal recessive"	Smarcd2 (MGI:1933621)			
chr17	63857015	63864378	17q23.3	17q23.3		612756	TCAM1	Testicular cell adhesion molecule 1	TCAM1P	146771							
chr17	63872011	63873728	17q22-q24	17q23.3		118820	"CSH2, CSB"	Chorionic somatomammotropin B	CSH2	1443	ENSG00000213218						
chr17	63880211	63881941	17q22-q24	17q23.3		139240	"GH2, GHV"	Growth hormone-2	GH2	2689	ENSG00000136487						
chr17	63894907	63896660	17q22-q24	17q23.3		150200	"CSH1, CSA, PL"	Chorionic somatomammotropin hormone-1	CSH1	1442	ENSG00000136488		[Placental lactogen deficiency] (1)				
chr17	63909596	63911327	17q22-q24	17q23.3		603515	"CSHL1, CSL"	Chorionic somatomammotropin hormone-like 1	CSHL1	1444	ENSG00000204414			Gh (MGI:95707)			
chr17	63917192	63918851	17q22-q24	17q23.3		139250	"GH1, GHN, IGHD1B"	Growth hormone-1	GH1	2688	ENSG00000259384	5'-GH1-CSHP1-CSH1-GH2-CSH2-3'	"Growth hormone deficiency, isolated, type IA, 262400 (3), Autosomal recessive; Growth hormone deficiency, isolated, type IB, 612781 (3); Growth hormone deficiency, isolated, type II, 173100 (3), Autosomal dominant; Kowarski syndrome, 262650 (3), Autosomal recessive"				
chr17	63928735	63932353	17q23	17q23.3		147245	"CD79B, IGB, B29, AGM6"	CD79B antigen	CD79B	974	ENSG00000007312		"Agammaglobulinemia 6, 612692 (3), Autosomal recessive"	Cd79b (MGI:96431)			
chr17	63938553	63972917	17q23.1-q25.3	17q23.3		603967	"SCN4A, HYPP, NAC1A, HOKPP2, CMS16"	"Sodium channel, voltage-gated, type IV, alpha polypeptide"	SCN4A	6329	ENSG00000007314	21.5kb from GH1	"Hyperkalemic periodic paralysis, type 2, 170500 (3), Autosomal dominant; Hypokalemic periodic paralysis, type 2, 613345 (3), Autosomal dominant; Myasthenic syndrome, congenital, 16, 614198 (3), Autosomal recessive; Myotonia congenita, atypical, acetazolamide-responsive, 608390 (3), Autosomal dominant; Paramyotonia congenita, 168300 (3), Autosomal dominant"	Scn4a (MGI:98250)			
chr17	64002594	64020633	17q23-q25	17q23.3		146630	ICAM2	Intercellular adhesion molecule-2	ICAM2	3384	ENSG00000108622			Icam2 (MGI:96394)			
chr17	64039141	64132468	17q23.3	17q23.3		604033	"ERN1, IRE1, IRE1A"	Endoplasmic reticulum-to-nucleus signaling 1	ERN1	2081	ENSG00000178607			Ern1 (MGI:1930134)			
chr17	64319414	64413843	17q23	17q23.3		173445	PECAM1	Platelet/endothelial cell adhesion molecule (CD31 antigen)	PECAM1	5175	ENSG00000261371			Pecam1 (MGI:97537)			
chr17	64477784	64497065	17q23-q24	17q23.3		604983	"POLG2, POLGB, PEOA4"	"Polymerase, DNA, gamma-2"	POLG2	11232	ENSG00000256525		"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, 610131 (3), Autosomal dominant"	Polg2 (MGI:1354947)			
chr17	64498253	64507037	17q23-q25	17q23.3		180630	"DDX5, HLR1, G17P1"	"DEAD/H box-5 (RNA helicase, 68kD)"	DDX5	1655	ENSG00000108654	near BRCA1		Ddx5 (MGI:105037)			
chr17	64542281	64662267	17q23.3-q24.1	17q23.3-q24.1		605532	SMURF2	SMAD-specific E3 ubiquitin protein ligase 2	SMURF2	64750	ENSG00000108854			Smurf2 (MGI:1913563)			
chr17	64600000	72900000	17q24			115660	"CTRCT7, CCA1"	Cataract 7	CCA1	878			"Cataract 7, 115660 (2), Autosomal dominant"				
chr17	64600000	72900000	17q24			616425	SRXY10	"46,XY sex reversal 10"				deletion of 32.5kb XYSR regulatory region upstream of SOX9	"46XY sex reversal 10, 616425 (4), Autosomal dominant"				
chr17	64854133	64919490	17q24.1	17q24.1		616557	LRRC37A3	Leucine-rich repeat-containing protein 37A3	LRRC37A3	374819	ENSG00000176809						
chr17	65009288	65056801	17q24.3	17q24.1		604406	GNA13	"Guanine nucleotide-binding protein, alpha-13"	GNA13	10672	ENSG00000120063			Gna13 (MGI:95768)			
chr17	65137337	65227702	17q23-q24	17q24.1		604067	"RGS9, PERRS"	Regulator of G protein signaling 9	RGS9	8787	ENSG00000108370		"Bradyopsia, 608415 (3)"	Rgs9 (MGI:1338824)			
chr17	65528562	65561621	17q24	17q24.1		604025	"AXIN2, ODCRCS"	"Axis inhibitor 2 (conductin, mouse, homolog of)"	AXIN2	8313	ENSG00000168646		"Colorectal cancer, somatic, 114500 (3); Oligodontia-colorectal cancer syndrome, 608615 (3), Autosomal dominant"	Axin2 (MGI:1270862)			
chr17	66200000	72900000	17q24.2-q24.3			135400	"HTGH, DEL17q24"	"Hypertrichosis terminalis, generalized, with or without gingival hyperplasia (chromosome 17q24 microdeletion syndrome)"					"Hypertrichosis terminalis, generalized, with or without gingival hyperplasia, 135400 (4), Autosomal recessive"				
chr17	66212028	66229437	17q23-qter	17q24.2		138700	APOH	Apolipoprotein H (beta-2-glycoprotein I)	APOH	350	ENSG00000091583			Apoh (MGI:88058)			
chr17	66302639	66810743	17q22-q23.2	17q24.2		176960	"PRKCA, PKCA"	"Protein kinase C, alpha polypeptide"	PRKCA	5578	ENSG00000154229	cen-COL1A1-PKCA-GH1	"Pituitary tumor, invasive (3)"	Prkca (MGI:97595)			
chr17	66877272	66885277	17q24	17q24.2		606405	CACNG5	"Calcium channel, voltage-dependent, gamma-5 subunit"	CACNG5	27091	ENSG00000075429			Cacng5 (MGI:2157946)			
chr17	67044535	67056796	17q24	17q24.2		114209	"CACNG1, CACNLG"	"Calcium channel, voltage-dependent, gamma-1 subunit"	CACNG1	786	ENSG00000108878			Cacng1 (MGI:1206582)			
chr17	67070437	67245988	17q24.2	17q24.2		606699	"HELZ, KIAA0054, HUMORF5"	Helicase with zinc finger domain	HELZ	9931	ENSG00000198265			Helz (MGI:1925705)			
chr17	67337915	67366626	17q24.2	17q24.2		604450	"PSMD12, P55, STISS"	"Proteasome 26S subunit, non-ATPase, 12"	PSMD12	5718	ENSG00000197170		"Stankiewicz-Isidor syndrome, 617516 (3), Autosomal dominant"	Psmd12 (MGI:1914247)			
chr17	67377280	67697262	17q24.2	17q24.2		605134	"PITPNC1, RDGBB"	"Phosphatidylinositol transfer protein, cytoplasmic, 1"	PITPNC1	26207	ENSG00000154217						
chr17	67717832	67744207	17q24.2	17q24.2		615366	NOL11	Nucleolar protein 11	NOL11	25926	ENSG00000130935			Nol11 (MGI:1916229)			
chr17	67825516	67984377	17q24	17q24.2		601819	"BPTF, FALZ, FAC1, NURF301, NEDDFL"	Bromodomain PHD finger transcription factor	BPTF	2186	ENSG00000171634		"Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, 617755 (3), Autosomal dominant"	Bptf (MGI:2444008)			
chr17	68035601	68046858	17q23-q24	17q24.2		600685	"KPNA2, RCH1, QIP2"	Karyopherin alpha-2	KPNA2	3838	ENSG00000182481			Kpna2 (MGI:103561)			
chr17	68205485	68257163	17q24.2	17q24.2		615169	AMZ2	Archaelysin family metallopeptidase 2	AMZ2	51321	ENSG00000196704						
chr17	68259181	68452004	17q24.2	17q24.2		610008	"ARSG, KIAA1001"	Arylsulfatase G	ARSG	22901	ENSG00000141337			Arsg (MGI:1921258)			
chr17	68413622	68551315	17q23-q24	17q24.2		188830	"PRKAR1A, TSE1, CNC1, CAR, PPNAD1, ACRDYS1"	"Protein kinase, cAMP-dependent, regulatory, type I, alpha"	PRKAR1A	5573	ENSG00000108946	fused with RET to form PTC2	"Acrodysostosis 1, with or without hormone resistance, 101800 (3), Autosomal dominant; Adrenocortical tumor, somatic (3); Carney complex, type 1, 160980 (3), Autosomal dominant; Myxoma, intracardiac, 255960 (3), Autosomal dominant; Pigmented nodular adrenocortical disease, primary, 1, 610489 (3), Autosomal dominant"	Prkar1a (MGI:104878)			
chr17	68530275	68600953	17q24.2	17q24.2		611062	"FAM20A, AIGFS, AI1G"	"Family with sequence similarity 20, member A"	FAM20A	54757	ENSG00000108950		"Amelogenesis imperfecta, type IG (enamel-renal syndrome), 204690 (3), Autosomal recessive"	Fam20a (MGI:2388266)			
chr17	68867284	68955425	17q24.2	17q24.2		612505	"ABCA8, KIAA0822"	"ATP-binding cassette, subfamily A, member 8"	ABCA8	10351	ENSG00000141338			Abca8b (MGI:1351668)			
chr17	68974631	69078977	17q24.2	17q24.2		612507	ABCA9	"ATP-binding cassette, subfamily A, member 9"	ABCA9	10350	ENSG00000154258			Abca9 (MGI:2386796)			
chr17	69062043	69141926	17q24.2	17q24.2-q24.3		612504	ABCA6	"ATP-binding cassette, subfamily A, member 6"	ABCA6	23460	ENSG00000154262			Abca6 (MGI:1923434)			
chr17	69100000	76800000	17q24.3-q25.1			261800	PRBNS	Pierre Robin syndrome		100301572		between D17S795 and D17S929	"Pierre Robin syndrome, 261800 (2), Autosomal recessive"				
chr17	69100000	76800000	17q24.3-q25.1			278850	"SRXX2, DUP17q24.3"	46XX sex reversal 2				duplication or triplication of 68kb XXSR regulatory region upstream of SOX9	"46XX sex reversal 2, 278850 (4), Autosomal dominant"				
chr17	69100000	72900000	17q24.3			614834	TTPP3	"Thyrotoxic periodic paralysis, susceptibility to, 3"		112272595		associated with rs312691	"{Thyrotoxic periodic paralysis, susceptibility to, 3}, 614834 (2)"				
chr17	69148006	69244814	17q24.2	17q24.3		612508	ABCA10	"ATP-binding cassette, subfamily A, member 10"	ABCA10	10349	ENSG00000154263						
chr17	69244434	69327181	17q24.2	17q24.3		612503	"ABCA5, KIAA1888"	"ATP-binding cassette, subfamily A, member 5"	ABCA5	23461	ENSG00000154265			Abca5 (MGI:2386607)			
chr17	69414696	69553860	17q24.3	17q24.3		601254	"MAP2K6, PRKMK6, MKK6, MEK6, MAPKK6"	Mitogen-activated protein kinase kinase 6	MAP2K6	5608	ENSG00000108984			Map2k6 (MGI:1346870)			
chr17	70075224	70135607	17q25	17q24.3		605722	"KCNJ16, KIR5.1"	"Potassium channel, inwardly rectifying, subfamily J, member 16"	KCNJ16	3773	ENSG00000153822			Kcnj16 (MGI:1314842)			
chr17	70169534	70180043	17q23.1-q24.2	17q24.3		600681	"KCNJ2, HHIRK1, KIR2.1, IRK1, LQT7, SQT3, ATFB9"	"Potassium channel, inwardly rectifying, subfamily J, member 2"	KCNJ2	3759	ENSG00000123700		"Andersen syndrome, 170390 (3), Autosomal dominant; Atrial fibrillation, familial, 9, 613980 (3), Autosomal dominant; Short QT syndrome 3, 609622 (3)"	Kcnj2 (MGI:104744)			
chr17	72121019	72126419	17q24.3-q25.1	17q24.3		608160	"SOX9, CMD1, SRA1"	SRY (sex-determining region Y)-box 9	SOX9	6662	ENSG00000125398		"Acampomelic campomelic dysplasia, 114290 (3), Autosomal dominant; Campomelic dysplasia, 114290 (3), Autosomal dominant; Campomelic dysplasia with autosomal sex reversal, 114290 (3), Autosomal dominant"	Sox9 (MGI:98371)			
chr17	72403321	72592803	17q24.3	17q24.3		617079	"LINC00673, HILNC75, SLNCR, LUCAIR1"	Long intergenic noncoding RNA 673	LINC00673	100499467							
chr17	72645945	73092713	17q24.3-q25.1	17q24.3-q25.1		616508	"SLC39A11, ZIP11, C17orf26"	"Solute carrier family 39 (zinc transporter), member 11"	SLC39A11	201266	ENSG00000133195			Slc39a11 (MGI:1917056)			
chr17	72900000	83257441	17q25			602197	CDR3	Cerebellar degeneration-related autoantigen-3		8163							
chr17	72900000	83257441	17q25			614163	DSPS	"Delayed sleep phase syndrome, susceptibility to"				associated with rs28936679 in AANAT	"{Delayed sleep phase syndrome, susceptibility to}, 614163 (2), Autosomal dominant"				
chr17	72900000	83257441	17q25			603411	EPR1	Effector cell protease receptor 1									
chr17	72900000	83257441	17q25.1-q25.3			614149	NDNC9	"Nail disorder, nonsyndromic congenital, 9 (anonychia-onycholysis)"		100682325		max lod at D17S1301	"Nail disorder, nonsyndromic congenital, 9, 614149 (2), Autosomal recessive"				
chr17	73165020	73171954	17q24	17q25.1		182452	SSTR2	Somatostatin receptor-2	SSTR2	6752	ENSG00000180616			Sstr2 (MGI:98328)			
chr17	73193033	73208506	17q25.1	17q25.1		606973	"COG1, LDLB, KIAA1381, CDG2G"	Component of oligomeric golgi complex 1	COG1	9382	ENSG00000166685		"Congenital disorder of glycosylation, type IIg, 611209 (3)"	Cog1 (MGI:1333873)			
chr17	73283623	73312003	17q24-q25	17q25.1		605468	"CDC42EP4, BORG4"	CDC42 effector protein 4 (binder of Rho GTPases 4)	CDC42EP4	23580	ENSG00000179604			Cdc42ep4 (MGI:1929760)			
chr17	73334383	73644480	17q25.1	17q25.1		607217	"SDK2, KIAA1514"	"Sidekick, Drosophila, homolog of, 2"	SDK2	54549	ENSG00000069188			Sdk2 (MGI:2443847)			
chr17	74203655	74209879	17q	17q25.1		604182	RPL38	Ribosomal protein L38	RPL38	6169	ENSG00000172809			Rpl38 (MGI:1914921)			
chr17	74213556	74262019	17q25.1	17q25.1		608855	TTYH2	"Tweety, Drosophila, homolog of, 2"	TTYH2	94015	ENSG00000141540			Ttyh2 (MGI:2157091)			
chr17	74274209	74314883	17q25	17q25.1		605483	"DNAI2, CILD9"	"Dynein, axonemal, intermediate chain 2"	DNAI2	64446	ENSG00000171595		"Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 (3)"	Dnaic2 (MGI:2685574)			
chr17	74367505	74372599	17q25.1	17q25.1		609046	"GPR142, PGR2"	G protein-coupled receptor 142	GPR142	350383	ENSG00000257008			Gpr142 (MGI:2668437)			
chr17	74431349	74451657	17q25.1-q25.3	17q25.1		605949	"GPRC5C, RAIG3"	"G protein-coupled receptor, family C, group 5, member C"	GPRC5C	55890	ENSG00000170412			Gprc5c (MGI:1917605)			
chr17	74466372	74484797	17q24	17q25.1		606790	"CMRF35H, CMRF35H9"	CMRF35H antigen	CD300A	11314	ENSG00000167851			Cd300a (MGI:2443411)			
chr17	74521173	74531473	17q25.1	17q25.1		610705	"CD300LB, TREM5, IREM3"	"CD300 antigen-like family, member B"	CD300LB	124599	ENSG00000178789			Cd300lb (MGI:2685099)			
chr17	74534358	74546170	17q22-q24	17q25.1		606786	"CMRF35, CMRF35A"	CMRF35 antigen	CD300C	10871	ENSG00000167850			"Cd300c2,Cd300c (MGI:2153249,MGI:3032626)"			
chr17	74557228	74567511	17q25.1	17q25.1		616560	CD300H	CD300H antigen		100130520	ENSG00000284690						
chr17	74579364	74592282	17q25.1	17q25.1		616301	"CD300LD, CD300D"	"CD300 antigen-like family, member D"	CD300LD	100131439	ENSG00000204345			"Cd300ld,Cd300ld3,Cd300ld4,Cd300ld5 (MGI:3702661,MGI:2687214,MGI:2442358,MGI:3702658)"			
chr17	74609882	74623957	17q25.1	17q25.1		609801	"CD300E, CD300LE, IREM2, CLM2"	CD300E antigen	CD300E	342510	ENSG00000186407			Cd300e (MGI:2387602)			
chr17	74671116	74747334	17q25.1	17q25.1		609956	RAB37	Pas-associated protein RAB37	RAB37	326624	ENSG00000172794			Rab37 (MGI:1929945)			
chr17	74694307	74712999	17q25.1	17q25.1		609807	"CD300LF, IGSF13, IREM1, CLM1"	"CD300 antigen-like family, member F"	CD300LF	146722	ENSG00000186074			Cd300lf (MGI:2442359)			
chr17	74748611	74769359	17q25.1	17q25.1		604990	"SLC9A3R1, EBP50, NHERF1, NPHLOP2"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulatory factor 1"	SLC9A3R1	9368	ENSG00000109062		"Nephrolithiasis/osteoporosis, hypophosphatemic, 2, 612287 (3), Autosomal dominant"	Slc9a3r1 (MGI:1349482)			
chr17	74842020	74860842	17q25	17q25.1		138254	"GRIN2C, NMDAR2C"	"Glutamate receptor, ionotropic, N-methyl D-aspartate 2C"	GRIN2C	2905	ENSG00000161509			Grin2c (MGI:95822)			
chr17	74862496	74873030	17q24-q25	17q25.1		103270	"FDXR, ADXR, ANOA"	Ferredoxin reductase (adrenodoxin reductase)	FDXR	2232	ENSG00000161513		"Auditory neuropathy and optic atrophy, 617717 (3), Autosomal recessive"	Fdxr (MGI:104724)			
chr17	74916082	74923262	17q24-q25	17q25.1		607696	"SANS, USH1G"	Scaffold protein containing ankyrin repeats and SAM domain	USH1G	124590	ENSG00000182040	?allelic to DFNA20	"Usher syndrome, type 1G, 606943 (3), Autosomal recessive"	Ush1g (MGI:2450757)			
chr17	74922954	74933912	17q25.3	17q25.1		607827	OTOP2	Otopetrin 2	OTOP2	92736	ENSG00000183034			Otop2 (MGI:2388365)			
chr17	74935801	74949992	17q25.3	17q25.1		607828	OTOP3	Otopetrin 3	OTOP3	347741	ENSG00000182938			Otop3 (MGI:1916852)			
chr17	74950741	74972804	17q25.1	17q25.1		605752	"HID1, 17orf28, DMC1"	HID1 domain-containing protein 1	HID1	283987	ENSG00000167861			Hid1 (MGI:2445087)			
chr17	75012663	75021260	17q25.1	17q25.1		603000	"ICT1, DS1"	Immature colon carcinoma transcript 1	MRPL58	3396	ENSG00000167862			Mrpl58 (MGI:1915822)			
chr17	75032566	75065888	17q25.1	17q25.1		613422	"KCTD2, KIAA0176"	Potassium channel tetramerization domain-containing 2	KCTD2	23510	ENSG00000180901			Kctd2 (MGI:1917632)			
chr17	75130224	75131964	17q23-q25	17q25.1		191720	"NT5C, UMPH2, DNT1"	"5', 3' nucleotidase, cytosolic"	NT5C	30833	ENSG00000125458			Nt5c (MGI:1354954)			
chr17	75205435	75235758	17q25	17q25.1		170285	"NUP85, PCNT1, PCNT"	Nucleoporin 85kD	NUP85	79902	ENSG00000125450			Nup85 (MGI:3046173)			
chr17	75261667	75266375	17q23-q25	17q25.1		611974	"MRPS7, COXPD34"	Mitochondrial ribosomal protein S7	MRPS7	51081	ENSG00000125445	mutation identified in 1 COXPD34 family	"?Combined oxidative phosphorylation deficiency 34, 617872 (3), Autosomal recessive"	Mrps7 (MGI:1354367)			
chr17	75225463	75262392	Chr.17	17q25.1		606006	"GGA3, KIAA0154"	"Golgi associated, gamma adaptin ear containing, ARF binding protein 3"	GGA3	23163	ENSG00000125447			Gga3 (MGI:2384159)			
chr17	75266227	75271291	17q25.1	17q25.1		612072	"MIF4GD, SLIP1"	MIF4G domain-containing protein	MIF4GD	57409	ENSG00000125457			Mif4gd (MGI:1916924)			
chr17	75272979	75289957	17q25.3	17q25.1		606521	"SLC25A19, DNC, MUP1, MCPHA, THMD3, THMD4"	"Solute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19"	SLC25A19	60386	ENSG00000125454		"Microcephaly, Amish type, 607196 (3), Autosomal recessive; Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), 613710 (3), Autosomal recessive"	Slc25a19 (MGI:1914533)			
chr17	75318075	75405708	17q24-q25	17q25.1		108355	GRB2	Growth factor receptor-bound protein 2	GRB2	2885	ENSG00000177885			Grb2 (MGI:95805)			
chr17	75500259	75515582	17q25.1	17q25.1		612185	"CASKIN2, KIAA1139"	CASK-interacting protein 2	CASKIN2	57513	ENSG00000177303			Caskin2 (MGI:2157062)			
chr17	75516507	75524738	17q25.1	17q25.1		608755	"TSEN54, SEN54, PCH2A, PCH4, PCH5"	"tRNA splicing endonuclease 54, S. cerevisiae, homolog of"	TSEN54	283989	ENSG00000182173	mutation identified in 1 PCH5 patient	"Pontocerebellar hypoplasia type 2A, 277470 (3), Autosomal recessive; Pontocerebellar hypoplasia type 4, 225753 (3), Autosomal recessive; ?Pontocerebellar hypoplasia type 5, 610204 (3), Autosomal recessive"	Tsen54 (MGI:1923515)			
chr17	75626844	75667201	17q25	17q25.1		603781	"RECQL5, RECQ5"	"DNA helicase, RecQ-like 5"	RECQL5	9400	ENSG00000108469			Recql5 (MGI:2156841)			
chr17	75667115	75708061	17q25.1	17q25.1		610218	"SAP30BP, HTRP, HCNGP, HTRG"	SAP30-binding protein	SAP30BP	29115	ENSG00000161526			Sap30bp (MGI:1927479)			
chr17	75721327	75757818	17q11-qter	17q25.1		147557	ITGB4	"Integrin, beta-4"	ITGB4	3691	ENSG00000132470		"Epidermolysis bullosa of hands and feet, 131800 (3), Autosomal dominant; Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3), Autosomal recessive; Epidermolysis bullosa, junctional, with pyloric atresia, 226730 (3), Autosomal recessive"	Itgb4 (MGI:96613)			
chr17	75757936	75765198	17q24	17q25.1		604313	GALK1	Galactokinase-1	GALK1	2584	ENSG00000108479		"Galactokinase deficiency with cataracts, 230200 (3), Autosomal recessive"	Galk1 (MGI:95730)			
chr17	75776433	75779934	17q25	17q25.1		601058	H3F3B	"H3 histone, family 3B (H3.3B)"	H3F3B	3021	ENSG00000132475			"H3f3b,H3f3a (MGI:1101768,MGI:1097686)"			
chr17	75784770	75825804	17q25.1	17q25.1		616375	"UNK, UNKEMPT, ZC3H5, KIAA1753"	Unkempt family zinc finger protein	UNK	85451	ENSG00000132478			Unk (MGI:2442456)			
chr17	75827224	75844716	17q25.1	17q25.1		608897	"UNC13D, MUNC13-4, HPLH3, HLH3, FHL3"	"UNC13, C. elegans, homolog of, D"	UNC13D	201294	ENSG00000092929		"Hemophagocytic lymphohistiocytosis, familial, 3, 608898 (3)"	Unc13d (MGI:1917700)			
chr17	75845698	75856435	17q25	17q25.1		606962	"WBP2, DFNB107"	WW domain-binding protein 2	WBP2	23558	ENSG00000132471		"Deafness, autosomal recessive 107, 617639 (3), Autosomal recessive"	Wbp2 (MGI:104709)			
chr17	75874163	75878598	17q24-q25	17q25.1		611041	"TRIM47, GOA"	Tripartite motif-containing protein 47	TRIM47	91107	ENSG00000132481			Trim47 (MGI:1917374)			
chr17	75898642	75905099	17q23-q25	17q25.1		611844	MRPL38	Mitochondrial ribosomal protein L38	MRPL38	64978	ENSG00000204316			Mrpl38 (MGI:1926269)			
chr17	75909573	75938231	17q25.1	17q25.1		616807	"FGF1, ALB"	FAS-binding factor 1	FBF1	85302	ENSG00000188878			Fbf1 (MGI:1922033)			
chr17	75941506	75979433	17q25.1	17q25.1		609751	"ACOX1, ACOX, SCOX"	"Acyl-Coenzyme A oxidase 1, palmitoyl"	ACOX1	51	ENSG00000161533		"Peroxisomal acyl-CoA oxidase deficiency, 264470 (3), Autosomal recessive"	Acox1 (MGI:1330812)			
chr17	75979216	76000585	17q25.1	17q25.1		613130	"TEN1, C17orf106"	"TEN1, CST complex subunit"	TEN1	100134934	ENSG00000257949			Ten1 (MGI:1916785)			
chr17	76000905	76005998	17q22-qter	17q25.1		123828	CDK3	Cyclin-dependent kinase 3	CDK3	1018	ENSG00000250506	distal to BRCA1					
chr17	76006844	76027451	17q25	17q25.1		601590	EVPL	Envoplakin	EVPL	2125	ENSG00000167880			Evpl (MGI:107507)			
chr17	76038774	76072525	17q25.1	17q25.1		604858	SRP68	"Signal recognition particle, 68kD"	SRP68	6730	ENSG00000167881			Srp68 (MGI:1917447)			
chr17	76070823	76077540	17q25.3	17q25.1		603691	"GALR2, GALNR2"	Galanin receptor 2	GALR2	8811	ENSG00000182687			Galr2 (MGI:1337018)			
chr17	76079181	76082803	17q25.3	17q25.1		610935	"LGICZ1, ZAC, L2"	"Ligand-gated ion channel, zinc-activated, 1"	ZACN	353174	ENSG00000186919						
chr17	76080992	76103786	17q25.1	17q25.1		608163	"EXOC1, EX070, KIAA1067"	Exocyst complex component 7	EXOC7	23265	ENSG00000182473			Exoc7 (MGI:1859270)			
chr17	76136332	76141298	17q22-q25	17q25.1		602291	"FOXJ1, FKHL13, HFH4"	Forkhead box J1	FOXJ1	2302	ENSG00000129654			Foxj1 (MGI:1347474)			
chr17	76310735	76354201	17q24-q25	17q25.1		601249	PRPSAP1	Phosphoribosyl pyrophosphate synthetase-associated protein-1	PRPSAP1	5635	ENSG00000161542			Prpsap1 (MGI:1915013)			
chr17	76382976	76387859	17q25.2	17q25.1		603730	SPHK1	Sphingosine kinase	SPHK1	8877	ENSG00000176170			Sphk1 (MGI:1316649)			
chr17	76389457	76453233	17q25.1	17q25.1		617649	"UBE2O, KIAA1734"	Ubiquitin-conjugating enzyme E2O	UBE2O	63893	ENSG00000175931			Ube2o (MGI:2444266)			
chr17	76453350	76470796	17q25	17q25.1		600950	"AANAT, SNAT"	Arylalkylamine N-acetyltransferase	AANAT	15	ENSG00000129673			Aanat (MGI:1328365)			
chr17	76470892	76501439	17p25.1	17q25.1		614404	"RHBDF2, IRHOM2, TOC"	"Rhomboid 5, Drosophila, homolog of, 2"	RHBDF2	79651	ENSG00000129667		"Tylosis with esophageal cancer, 148500 (3), Autosomal dominant"	Rhbdf2 (MGI:2442473)			
chr17	76527347	76557691	17q25	17q25.1		608759	"CYGB, HGB, STAP"	Cytoglobin	CYGB	114757	ENSG00000161544			Cygb (MGI:2149481)			
chr17	76527585	76555338	17q22	17q25.1		610598	"PRCD, RP36"	"PRCD, Dog, homolog of"	PRCD	768206	ENSG00000214140		"Retinitis pigmentosa 36, 610599 (3)"				
chr17	76565378	76586127	17q25.1	17q25.1		610137	"ST6GALNAC2, SIAT7B, SAITL1"	"ST6 alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2"	ST6GALNAC2	10610	ENSG00000070731			St6galnac2 (MGI:107553)			
chr17	76617768	76643837	17q25.1	17q25.1		610138	"ST6GALNAC1, SIAT7A, STYI"	"ST6 alpha-N-aetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1"	ST6GALNAC1	55808	ENSG00000070526			St6galnac1 (MGI:1341826)			
chr17	76712829	76726798	17q25	17q25.1		604914	"JMJD6, PSR"	Jumonji domain containing 6 (phosphatidylserine receptor)	JMJD6	23210	ENSG00000070495			Jmjd6 (MGI:1858910)			
chr17	76725875	76733880	17q25.1	17q25.1		615262	"METTL23, C17orf95, MRT44"	Methyltransferase-like 23	METTL23	124512	ENSG00000181038		"Mental retardation, autosomal recessive 44, 615942 (3), Autosomal recessive"	Mettl23 (MGI:1921569)			
chr17	76734114	76737410	17q25	17q25.1		600813	"SRSF2, SFRS2, SC35"	Serine/arginine-rich splicing factor 2	SRSF2	6427	ENSG00000161547			Srsf2 (MGI:98284)			
chr17	76868485	76950388	17q25.3	17q25.2		612441	MGAT5B	"Alpha-1,6-mannosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase isozyme B"	MGAT5B	146664	ENSG00000167889			Mgat5b (MGI:3606200)			
chr17	77088642	77217100	17q25.1-q25.2	17q25.2-q25.3		601504	SEC14L	"SEC14, S. cerevisiae, like"	SEC14L1	6397	ENSG00000129657			Sec14l1 (MGI:1921386)			
chr17	77200000	83257441	17q25.3			605805	ATOD4	"Dermatitis, atopic, 4"				maximum lod at D17S1290	"{Dermatitis, atopic, susceptibility to, 4}, 605805 (2)"				
chr17	77200000	83257441	17q25.3			612239	IS5	"Scoliosis, idiopathic, susceptibility to, 5"		100190985		between D17S1806 and 17qter	"{Scoliosis, idiopathic, susceptibility to, 5}, 612239 (2)"				
chr17	77281409	77500595	17q25	17q25.3		604061	"SEPT9, MSF, MSF1, NAPB"	Septin 9	9-Sep	10801	ENSG00000184640		"Amyotrophy, hereditary neuralgic, 162100 (3), Autosomal dominant; Leukemia, acute myeloid, therapy-related (1); Ovarian carcinoma (1)"	Sept9 (MGI:1858222)			
chr17	77958852	78108834	17q25.3	17q25.3		610741	"TNRC6C, KIAA1582"	Trinucleotide repeat-containing gene 6C	TNRC6C	57690	ENSG00000078687			Tnrc6c (MGI:2443265)			
chr17	78108774	78132426	17q25	17q25.3		605828	"TMC6, EVER1, EV1"	Transmembrane channel-like 6	TMC6	11322	ENSG00000141524		"Epidermodysplasia verruciformis, 226400 (3), Autosomal recessive"	Tmc6 (MGI:1098686)			
chr17	78129297	78142967	17q25	17q25.3		605829	"TMC8, EVER2, EV2"	Transmembrane channel-like 8	TMC8	147138	ENSG00000167895	previously mapped to 2p24-p21	"Epidermodysplasia verruciformis, 226400 (3), Autosomal recessive"	Tmc8 (MGI:2669037)			
chr17	78168544	78172927	17q25	17q25.3		603926	SYNGR2	Synaptogyrin 2	SYNGR2	9144	ENSG00000108639	"pseudogene on 15q11; near EV1, EV2, TK1"		Syngr2 (MGI:1328324)			
chr17	78174078	78187203	17q25.2-q25.3	17q25.3		188300	TK1	Thymidine kinase-1	TK1	7083	ENSG00000167900			Tk1 (MGI:98763)			
chr17	78214195	78225634	17q25	17q25.3		603352	API4	Apoptosis inhibitor 4	BIRC5	332	ENSG00000089685			Birc5 (MGI:1203517)			
chr17	78356776	78360078	17q25.3	17q25.3		604176	"SOCS3, SSI3, CIS3"	Suppressor of cytokine signaling 3	SOCS3	9021	ENSG00000184557			Socs3 (MGI:1201791)			
chr17	78378617	78424658	17q25.3	17q25.3		614942	PGS1	Phosphatidylglycerophosphate synthase 1	PGS1	9489	ENSG00000087157			Pgs1 (MGI:1921701)			
chr17	78423696	78577435	17q25	17q25.3		610063	"DNAH17, DNEL2"	"Dynein, axonemal, heavy chain 17"	DNAH17	8632	ENSG00000187775			Dnah17 (MGI:1917176)			
chr17	78674046	78782341	17q25	17q25.3		182115	"CYTH1, D17S811E, SEC7"	Cytohesin 1	CYTH1	9267	ENSG00000108669			Cyth1 (MGI:1334257)			
chr17	78787380	78840839	17q25.3	17q25.3		612543	"USP36, KIAA1453"	Ubiquitin-specific protease 36	USP36	57602	ENSG00000055483			Usp36 (MGI:1919594)			
chr17	78852976	78925389	17q25	17q25.3		188825	TIMP2	Tissue inhibitor of metalloproteinase-2	TIMP2	7077	ENSG00000035862			Timp2 (MGI:98753)			
chr17	78971252	78979978	17q25	17q25.3		600626	LGALS3BP	"Lectin, galactoside-binding, soluble, 3 binding protein (galectin 6 binding protein)"	LGALS3BP	3959	ENSG00000108679			Lgals3bp (MGI:99554)			
chr17	78991715	79009816	17q25.3	17q25.3		613165	"CANT1, SCAN1, DBQD1, EDM7"	Calcium-activated nucleotidase 1	CANT1	124583	ENSG00000171302		"Desbuquois dysplasia 1, 251450 (3), Autosomal recessive; Epiphyseal dysplasia, multiple, 7, 617719 (3), Autosomal recessive"	Cant1 (MGI:1923275)			
chr17	79022933	79049787	17q25	17q25.3		610365	"C1QTNF1, GIP"	C1q- and tumor necrosis factor-related protein 1	C1QTNF1	114897	ENSG00000173918			C1qtnf1 (MGI:1919254)			
chr17	79074811	79088602	17q25.3	17q25.3		611898	"NAGLUEB, FLJ21865"	"N-acetylglucosaminidase, endo-beta"	ENGASE	64772	ENSG00000167280			Engase (MGI:2443788)			
chr17	79089344	79665599	17q25.3	17q25.3		616999	"RBFOX3, FOX3, NEUN, HRNBP3"	"RNA-binding protein FOX1, C. Elegans, homolog of, 3"	RBFOX3	146713	ENSG00000167281						
chr17	79730918	79742925	17q25.3	17q25.3		616997	ENPP7	Ectonucleotide pyrophosphatase/phosphodiesterase 7	ENPP7	339221	ENSG00000182156			Enpp7 (MGI:3027917)			
chr17	79776253	79787649	17q25	17q25.3		602770	"CBX2, M33, SRXY5"	"Chromobox homolog 2, Drosophila polycomb class"	CBX2	84733	ENSG00000173894	mutation identified in 1 SRXY5 patient	"?46XY sex reversal 5, 613080 (3), Autosomal recessive"	Cbx2 (MGI:88289)			
chr17	79794376	79797115	17q25.3	17q25.3		617354	"CBX8, PC3"	Chromobox homolog 8	CBX8	57332	ENSG00000141570			Cbx8 (MGI:1353589)			
chr17	79833155	79839413	17q25.3	17q25.3		603079	"CBX4, PC2"	"Chromobox homolog 4, Drosophila polycomb class"	CBX4	8535	ENSG00000141582			Cbx4 (MGI:1195985)			
chr17	79932342	80035874	17q25.3	17q25.3		616637	TBC1D16	"TBC1 domain family, member 16"	TBC1D16	125058	ENSG00000167291			Tbc1d16 (MGI:2652878)			
chr17	80036631	80100612	17q25.3	17q25.3		613799	"CCDC40, KIAA1640"	Coiled-coil domain-containing protein 40	CCDC40	55036	ENSG00000141519		"Ciliary dyskinesia, primary, 15, 613808 (3)"	Ccdc40 (MGI:2443893)			
chr17	80101525	80119881	17q25.2-q25.3	17q25.3		606800	GAA	"Glucosidase, acid alpha-"	GAA	2548	ENSG00000171298	distal to TK1	"Glycogen storage disease II, 232300 (3), Autosomal recessive"	Gaa (MGI:95609)			
chr17	80135213	80147182	17q25.3	17q25.3		608546	"DDX48, EIF4A3, MUK34, NMP265, KIAA0111, RCPS"	DEAD/H Box 48	EIF4A3	9775	ENSG00000141543		"Robin sequence with cleft mandible and limb anomalies, 268305 (3), Autosomal recessive"	Eif4a3 (MGI:1923731)			
chr17	80169991	80209330	17q25.3	17q25.3		607211	"CARD14, CARMA2, BIMP2, PSORS2, PSS1, PRP"	Caspase recruitment domain-containing protein 14	CARD14	79092	ENSG00000141527		"Pityriasis rubra pilaris, 173200 (3), Autosomal dominant; Psoriasis 2, 602723 (3), Autosomal dominant"	Card14 (MGI:2386258)			
chr17	80200667	80220399	17q25.3	17q25.3		605270	"SGSH, MPS3A, SFMD"	N-sulfoglucosamine sulfohydrolase (sulfamidase)	SGSH	6448	ENSG00000181523		"Mucopolysaccharidosis type IIIA (Sanfilippo A), 252900 (3), Autosomal recessive"	Sgsh (MGI:1350341)			
chr17	80220286	80253508	17q25	17q25.3		610117	SLC26A11	"Solute carrier family 26 (sulfate transporter), member 11"	SLC26A11	284129	ENSG00000181045			Slc26a11 (MGI:2444589)			
chr17	80260819	80398785	17q25	17q25.3		613768	"RNF213, ALO17, KIAA1618, MYMY2"	Ring finger protein 213	RNF213	57674	ENSG00000173821		"{Moyamoya disease 2, susceptibility to}, 607151 (3)"	Rnf213 (MGI:1289196)			
chr17	80466832	80476603	17q25.1-q25.2	17q25.3		602367	"NPTX1, NP1"	"Pentraxin I, neuronal"	NPTX1	4884	ENSG00000171246			Nptx1 (MGI:107811)			
chr17	80544824	80966372	17q25.3	17q25.3		607130	"RPTOR, RAPTOR, KIAA1303"	Regulatory-associated protein of MTOR	RPTOR	57521	ENSG00000141564			Rptor (MGI:1921620)			
chr17	80991840	81000132	17q25.3	17q25.3		610901	CHMP6	"CHMP family, member 6"	CHMP6	79643	ENSG00000176108			Chmp6 (MGI:3583942)			
chr17	81035130	81117431	17q25	17q25.3		605475	"BAIAP2, IRSP53"	BAI1-associated protein 2	BAIAP2	10458	ENSG00000175866			Baiap2 (MGI:2137336)			
chr17	81117294	81166071	17q25.3	17q25.3		605276	"AATK, AATYK"	Apoptosis-associated tyrosine kinase	AATK	9625	ENSG00000181409			Aatk (MGI:1197518)			
chr17	81125882	81125948	17q25.3	17q25.3		614059	"MIR338, MIRN338"	Micro RNA 338	MIR338	442906							
chr17	81189592	81222988	17q25.3	17q25.3		613479	"AZI1, ZA1, KIAA1118"	"5-azacytidine-induced gene 1, mouse, homolog of"	CEP131	22994	ENSG00000141577			Cep131 (MGI:107440)			
chr17	81244810	81295432	17q25.3	17q25.3		616525	SLC38A10	"Solute carrier family 38 (amino acid transporter), member 10"	SLC38A10	124565	ENSG00000157637			Slc38a10 (MGI:1919305)			
chr17	81395430	81466331	17q25.3	17q25.3		617646	"BAHCC1, BAHD2, KIAA1447"	BAH domain- and coiled-coil domain-containing protein 1	BAHCC1	57597	ENSG00000266074			Bahcc1 (MGI:2679272)			
chr17	81509970	81512865	17q25.3	17q25.3		102560	"ACTG1, DFNA20, DFNA26, BRWS2"	"Actin, gamma-1"	ACTG1	71	ENSG00000184009		"Baraitser-Winter syndrome 2, 614583 (3), Autosomal dominant; Deafness, autosomal dominant 20/26, 604717 (3), Autosomal dominant"	Actg1 (MGI:87906)			
chr17	81513018	81537129	17q25	17q25.3		607643	"FSCN2, RFSN, RP30"	"Fascin, sea urchin, homolog of, 2"	FSCN2	25794	ENSG00000186765	within 200kb of ACTG1	"Retinitis pigmentosa 30, 607921 (3)"	Fscn2 (MGI:2443337)			
chr17	81539884	81552402	17q25.3	17q25.3		611301	"C17orf70, FAAP100"	Chromosome 17 open reading frame 70	FAAP100	80233	ENSG00000185504			Faap100 (MGI:1919135)			
chr17	81556884	81637152	17qter	17q25.3		606590	"NPL4, KIAA1499"	"Npl4, S. cerevisiae, homolog of"	NPLOC4	55666	ENSG00000182446			Nploc4 (MGI:2679787)			
chr17	81650458	81663417	17q25	17q25.3		180073	"PDE6G, PDEG, RP57"	"Phosphodiesterase-6G, cGMP-specific, rod, gamma"	PDE6G	5148	ENSG00000185527		"Retinitis pigmentosa 57, 613582 (3), Autosomal recessive"	Pde6g (MGI:97526)			
chr17	81666696	81673906	17q25.3	17q25.3		614271	CCDC137	Coiled-coil domain-containing protein 137	CCDC137	339230	ENSG00000185298			Ccdc137 (MGI:1914541)			
chr17	81683931	81702120	17q25	17q25.3		604375	"HGS, HRS"	Human growth factor-regulated tyrosine kinase substrate	HGS	9146	ENSG00000185359			Hgs (MGI:104681)			
chr17	81703369	81707525	17q25-qter	17q25.3		602375	"MRPL12, RPML12"	"Ribosomal protein, mitochondrial, L12"	MRPL12	6182	ENSG00000262814			Mrpl12 (MGI:1926273)			
chr17	81712235	81721015	17q25.3	17q25.3		606794	"SLC25A10, DIC"	"Solute carrier family 25 (mitochondrial carrier), member 10 (dicarboxylate ion carrier)"	SLC25A10	1468	ENSG00000183048			Slc25a10 (MGI:1353497)			
chr17	81804077	81814012	17q25	17q25.3		138033	GCGR	Glucagon receptor	GCGR	2642	ENSG00000215644		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant"	Gcgr (MGI:99572)			
chr17	81822360	81833293	17q25.3	17q25.3		616514	"FAM195B, MCRIP1"	"Family with sequence similarity 194, member B"	MCRIP1	348262	ENSG00000225663			Mcrip1 (MGI:2384752)			
chr17	81843157	81860667	17q25	17q25.3		176790	"P4HB, PROHB, CLCRP1"	"Procollagen-proline, 2-oxoglutarate-4-dioxygenase, beta polypeptide"	P4HB	5034	ENSG00000185624		"Cole-Carpenter syndrome 1, 112240 (3), Autosomal dominant"	P4hb (MGI:97464)			
chr17	81867718	81871405	17q25.3	17q25.3		601925	"ARHGDIA, GDIA1, NPHS8"	Rho GDP dissociation inhibitor (GDI) alpha	ARHGDIA	396	ENSG00000141522		"Nephrotic syndrome, type 8, 615244 (3), Autosomal recessive"	Arhgdia (MGI:2178103)			
chr17	81887834	81891621	17q25.3	17q25.3		604171	"ALYREF, THOC4, ALY, BEF"	ALY/REF export factor	ALYREF	10189	ENSG00000183684						
chr17	81890789	81900532	17q25.3	17q25.3		614534	"ANAPC11, APC11"	Anaphase-promoting complex subunit 11	ANAPC11	51529	ENSG00000141552			Anapc11 (MGI:1913406)			
chr17	81902108	81902904	17q25.3	17q25.3		607996	"NPB, PPL7"	Neuropeptide B	NPB	256933	ENSG00000183979			Npb (MGI:2387153)			
chr17	81911938	81918181	17q25.3	17q25.3		606212	"SIRT7, SIR2L7"	"Sirtuin 7 (Sir2, S. cerevisiae, homolog of, 7)"	SIRT7	51547	ENSG00000187531			Sirt7 (MGI:2385849)			
chr17	81918268	81927710	17q25	17q25.3		602020	MAFG	"v-maf avian musculoaponeurotic fibrosarcoma oncogene family, protein G"	MAFG	4097	ENSG00000197063			Mafg (MGI:96911)			
chr17	81932383	81937327	17q25.3	17q25.3		179035	"PYCR1, PRO3, ARCL2B, ARCL3B"	Pyrroline-5-carboxylate reductase-1	PYCR1	5831	ENSG00000183010		"Cutis laxa, autosomal recessive, type IIB, 612940 (3), Autosomal recessive; Cutis laxa, autosomal recessive, type IIIB, 614438 (3)"	Pycr1 (MGI:2384795)			
chr17	81952506	81961180	17q25.3	17q25.3		609847	NOTUM	"Notum, Drosophila, homolog of"	NOTUM	147111	ENSG00000185269			Notum (MGI:1924833)			
chr17	81977545	82017668	17q25	17q25.3		606236	"ASPSCR1, RCC17, ASPL, ASPS"	"Alveolar soft-part sarcoma chromosome region, candidate 1"	ASPSCR1	79058	ENSG00000169696	t(X;17)(p11.2;q25)	"Alveolar soft-part sarcoma, 606243 (3)"	Aspscr1 (MGI:1916188)			
chr17	82018702	82022929	17q25.3	17q25.3		615128	"STRA13, CENPX, FAAP10, MHF2, D9"	Stimulated by retinoic acid 13	CENPX	201254	ENSG00000169689			Cenpx (MGI:894324)			
chr17	82031655	82034203	17q25.3	17q25.3		602050	RAC3	"Ras-related C3 botulinum toxin substrate-3 (rho family, small GTP-binding protein Rac3)"	RAC3	5881	ENSG00000169750			Rac3 (MGI:2180784)			
chr17	82035880	82037696	17q25.3	17q25.3		608347	"DCXR, P34H, PNTSU"	Dicarbonyl/L-xylulose reductase	DCXR	51181	ENSG00000169738		"[Pentosuria], 260800 (3), Autosomal recessive"	Dcxr (MGI:1915130)			
chr17	82047901	82051773	17q25	17q25.3		602578	RFNG	Radical fringe	RFNG	5986	ENSG00000169733			Rfng (MGI:894275)			
chr17	82051464	82058060	17q25.3	17q25.3		601934	GPS1	G protein pathway suppressor 1	GPS1	2873	ENSG00000169727			Gps1 (MGI:2384801)			
chr17	82078337	82098302	17q25	17q25.3		600212	FASN	Fatty acid synthase	FASN	2194	ENSG00000169710			Fasn (MGI:95485)			
chr17	82239018	82273741	17q25	17q25.3		600864	"CSNK1D, ASPS, FASPS2"	"Casein kinase-1, delta"	CSNK1D	1453	ENSG00000141551		"Advanced sleep-phase syndrome, familial, 2, 615224 (3), Autosomal dominant"	Csnk1d (MGI:1355272)			
chr17	82314864	82320828	17q25.2-q25.3	17q25.3		186820	CD7	CD7 antigen (p41)	CD7	924	ENSG00000173762			Cd7 (MGI:88344)			
chr17	82321023	82334044	17q25.2-q25.3	17q25.3		602602	"SECTM1, K12"	Secreted and transmembrane 1	SECTM1	6398	ENSG00000141574			Sectm1a (MGI:2384805)			
chr17	82359246	82363775	17q25.3	17q25.3		615647	TEX19	Testis-expressed gene 19	TEX19	400629	ENSG00000182459			Tex19.2 (MGI:1918206)			
chr17	82374276	82375585	17q25.3	17q25.3		600896	"GPR14, UTR2, UTR"	G protein-coupled receptor-14 (urotensin II receptor)	UTS2R	2837	ENSG00000181408			Uts2r (MGI:2183450)			
chr17	82519717	82604606	17q25	17q25.3		147685	"FOXK2, ILF1"	Forkhead box K2 (interleukin enhancer-binding factor 1)	FOXK2	3607	ENSG00000141568			Foxk2 (MGI:1916087)			
chr17	82614561	82648534	17q25.3	17q25.3		609226	"WDR45B, WIPI3, WDR45L"	WD repeat domain 45B	WDR45B	56270	ENSG00000141580			Wdr45b (MGI:1914090)			
chr17	82716705	82728016	17q25	17q25.3		611683	FN3KRP	Fructosamine 3-kinase-related protein	FN3KRP	79672	ENSG00000141560			Fn3krp (MGI:2679256)			
chr17	82735575	82751196	17q25.3	17q25.3		608425	FN3K	Fructosamine 3-kinase	FN3K	64122	ENSG00000167363			Fn3k (MGI:1926834)			
chr17	82752047	82943185	17q25	17q25.3		604649	"TBCD, PEBAT"	Tubulin-specific chaperone D	TBCD	6904	ENSG00000141556		"Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum, 617193 (3), Autosomal recessive"	Tbcd (MGI:1919686)			
chr17	82829433	82840054	17q25.3	17q25.3		610226	"ZNF750, FLJ13841"	Zinc finger protein 750	ZNF750	79755	ENSG00000141579		"Seborrhea-like dermatitis with psoriasiform elements, 610227 (3)"	Zfp750 (MGI:2442210)			
chr17	82942148	83051844	17q25.3	17q25.3		615337	B3GNTL1	"Beat-1,3-N-acetylglucosaminyltransferase-like 1"	B3GNTL1	146712	ENSG00000175711			B3gntl1 (MGI:2441705)			
chr17	83079690	83095125	17q25.3	17q25.3		616241	METRNL	Meteorin-like protein	METRNL	284207	ENSG00000176845			Metrnl (MGI:2384806)			
chr17	0	83257441	Chr.17			138110	G6PDL	Glucose-6-phosphate dehydrogenase-like									
chr17	0	83257441	Chr.17			610064	ODS1	"Opioid dependence, susceptibility to, 1"		100188802			"{Opioid dependence, susceptibility to, 1}, 610064 (2)"				
chr18	0	15400000	18p11.3-p11.2			104000	AA1	Alopecia areata 1		100034700		max lod at D18S967	"Alopecia areata 1, 104000 (2), Multifactorial"				
chr18	0	18500000	18p			146390	"DEL18p, C18DELp"	Chromosome 18p deletion syndrome					"Chromosome 18p deletion syndrome, 146390 (4), Autosomal dominant"				
chr18	0	7200000	18p11.32-p11.31			609647	DFNB46	"Deafness, neurosensory, autosomal recessive 46"	DFNB46	449488		between D18S59 and D18S391	"Deafness, autosomal recessive 46, 609647 (2), Autosomal recessive"				
chr18	0	18500000	18p11			607488	DYT15	"Dystonia-15, myoclonic"	DYT15	317714			"Dystonia-15, myoclonic, 607488 (2), Autosomal dominant"				
chr18	0	18500000	18p			602124	DYT7	"Dystonia-7 (torsion dystonia, adult-onset, focal)"	DYT7	1866			"Dystonia-7, torsion, 602124 (2), Autosomal dominant"				
chr18	0	15400000	18pter-p11.21			131150	ERV1	Oncogene ERV1; endogenous retrovirus-1									
chr18	0	18500000	18p11			612354	IBD21	Inflammatory bowel disease 21		100192312		associated with rs2542151	"{Inflammatory bowel disease 21}, 612354 (2), Autosomal dominant"				
chr18	0	18500000	18p			125480	"MAFD1, BPAD, MD1"	Major affective disorder 1	MAFD1	4095		?also 18q	"{Major affective disorder 1}, 125480 (2), Autosomal dominant"				
chr18	0	7200000	18p11.3			614343	MRT19	"Mental retardation, autosomal recessive 19"	MRT19	100852395		between rs4606805 and rs1787846	"Mental retardation, autosomal recessive 19, 614343 (2), Autosomal recessive"				
chr18	0	7200000	18p11.3			612353	"POROK6, DSAP4"	Porokeratosis 6		100196911		between telomere and D18S391	"Porokeratosis 6, multiple types, 612353 (2), Autosomal dominant"				
chr18	0	18500000	18p			603206	SCZD8	"Schizophrenia susceptibility locus, chromosome 18-related"	SCZD8	8806			"{Schizophrenia}, 181500 (2), Autosomal dominant"				
chr18	0	18500000	18p			614290	TET18P	Tetrasomy 18p					"Tetrasomy 18p, 614290 (4)"				
chr18	158482	213738	18p	18p11.32		607274	"USP14, TGT"	Ubiquitin-specific protease 14	USP14	9097	ENSG00000101557			Usp14 (MGI:1928898)			
chr18	214347	268058	18p11.32	18p11.32		606930	"THOC1, HPR1"	THO complex 1 (nuclear matrix protein p84)	THOC1	9984	ENSG00000079134			Thoc1 (MGI:1919668)			
chr18	319354	500728	18p11.32	18p11.32		607621	"COLEC12, SRCL, CLP1"	Collectin 12	COLEC12	81035	ENSG00000158270			Colec12 (MGI:2152907)			
chr18	580342	582019	18p11.32	18p11.32		603187	"CETN1, CEN1"	Centrin-1	CETN1	1068	ENSG00000177143			Cetn1 (MGI:1347086)			
chr18	596997	650297	18p11.3	18p11.32		616990	CLUL1	Clusterin-like protein 1	CLUL1	27098	ENSG00000079101						
chr18	657583	673577	18p11.32	18p11.32		188350	"TYMS, TS, TMS"	Thymidylate synthase	TYMS	7298	ENSG00000176890	<50 kb from YES1		Tyms (MGI:98878)			
chr18	670319	712663	18p11.32	18p11.32		607427	"ENOSF1, RTS"	Enolase superfamily member 1	ENOSF1	55556	ENSG00000132199						
chr18	721591	812845	18p11.3	18p11.32		164880	YES1	Oncogene YES-1	YES1	7525	ENSG00000176105	<50 kb from TYMS		Yes1 (MGI:99147)			
chr18	904383	912171	18p11	18p11.32		102980	ADCYAP1	Adenylate cyclase activating polypeptide-1 (pituitary)	ADCYAP1	116	ENSG00000141433			Adcyap1 (MGI:105094)			
chr18	2655886	2805016	18p11.32	18p11.32		614982	"SMCHD1, KIAA0650, BAMS"	Structural maintenance of chromosomes flexible hinge domain-containing protein 1	SMCHD1	23347	ENSG00000101596		"Bosma arhinia microphthalmia syndrome, 603457 (3), Autosomal dominant; Fascioscapulohumeral muscular dystrophy 2, digenic, 158901 (3)"	Smchd1 (MGI:1921605)			
chr18	2900000	7200000	18p11.31			160700	MYP2	"Myopia, high grade, autosomal dominant 1"	MYP2	4658			"Myopia-2, 160700 (2), Autosomal dominant"				
chr18	2916993	3013314	18p	18p11.31		605519	LPIN2	Lipin 2	LPIN2	9663	ENSG00000101577		"Majeed syndrome, 609628 (3)"	Lpin2 (MGI:1891341)			
chr18	3066806	3220107	18p11.31	18p11.31		603508	"MYOM1, SKELEMIN"	Myomesin 1	MYOM1	8736	ENSG00000101605			Myom1 (MGI:1341430)			
chr18	3262112	3278283	18p11.31	18p11.31		609211	"MYL12B, MRLC2"	"Myosin, light chain 12B, regulatory"	MYL12B	103910	ENSG00000118680			Myl12a (MGI:1914518)			
chr18	3411926	3458411	18p11.3	18p11.31		602630	"TGIF1, HPE4"	TG-interacting factor 1	TGIF1	7050	ENSG00000177426		"Holoprosencephaly 4, 142946 (3), Autosomal dominant"	Tgif1 (MGI:1194497)			
chr18	3496031	4455440	18p11.31	18p11.31		605445	"DLGAP1, DAP1, DLGAP1A, DLGAP1B"	Discs large-associated protein 1	DLGAP1	9229	ENSG00000170579			Dlgap1 (MGI:1346065)			
chr18	5142910	5197751	18p11.31	18p11.31		616427	C18orf42	Chromosome 18 open reading frame 42	AKAIN1	642597	ENSG00000231824			Akain1 (MGI:2444600)			
chr18	5289018	5297052	18p11.21	18p11.31		602126	"ZFP161, ZF5"	Zinc finger protein-161	ZBTB14	7541	ENSG00000198081			Zbtb14 (MGI:1195345)			
chr18	5392275	5630662	18p11.3	18p11.31		605331	"EPB41L3, DAL1"	Erythrocyte membrane protein band 4.1-like 3	EPB41L3	23136	ENSG00000082397			Epb41l3 (MGI:103008)			
chr18	5954702	6414918	18p11.31	18p11.31		617135	L3MBTL4	L3MBT-like 4	L3MBTL4	91133	ENSG00000154655			L3mbtl4 (MGI:2444889)			
chr18	6729717	6915715	18p11.31	18p11.31		610592	"ARHGAP28, KIAA1314"	RHO GTPase-activating protein 28	ARHGAP28	79822	ENSG00000088756			Arhgap28 (MGI:2147003)			
chr18	6941743	7117813	18p11.31	18p11.31		150320	"LAMA1, PTBHS"	"Laminin, alpha-1"	LAMA1	284217	ENSG00000101680		"Poretti-Boltshauser syndrome, 615960 (3), Autosomal recessive"	Lama1 (MGI:99892)			
chr18	7200000	39500000	18p11.23-q12.2			107200	ANIC	"Anosmia, isolated congenital"		550625		max lod at D18S1108	"Anosmia, isolated congenital, 107200 (2), Autosomal dominant"				
chr18	7200000	15400000	18p11.2			606616	"DYX6, DYXQTL18"	"Dyslexia, susceptibility to, 6"	DYX6	266691			"{Dyslexia, susceptibility to, 6}, 606616 (2)"				
chr18	7200000	15400000	18p11.2			609253	6-Feb	"Febrile seizures, familial, 6"	6-Feb	619397		max lod at D18S1158	"Febrile seizures, familial, 6, 609253 (2), Autosomal dominant"				
chr18	7200000	8500000	18p11.23			612410	PSORS10	Psoriasis susceptibility 10	PSORS10	503613		between D18S63 and D18S967	"{Psoriasis susceptibility 10}, 612410 (2)"				
chr18	7567315	8406860	18p11.2	18p11.23		176888	"PTPRM, PTPRL1, RPTPM"	"Protein tyrosine phosphatase, receptor type, mu polypeptide"	PTPRM	5797	ENSG00000173482			Ptprm (MGI:102694)			
chr18	8609427	8639382	18p11.22	18p11.22		616448	RAB12	Ras-associated protein RAB12	RAB12	201475	ENSG00000206418			Rab12 (MGI:894284)			
chr18	8695855	8707620	18p11.22	18p11.22		616131	"GACAT2, MTCL1AS1"	"Gastric cancer-associated transcript 2, noncoding"	GACAT2	100287082							
chr18	8706053	8832777	18p11.22	18p11.22		615766	"MTCL1, KIAA0802"	Microtubule crosslinking factor 1	MTCL1	23255	ENSG00000168502			Mtcl1 (MGI:1915867)			
chr18	9102629	9134344	18p11.31-p11.2	18p11.22		600532	NDUFV2	"NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kD"	NDUFV2	4729	ENSG00000178127	pseudogene on 19q13.3-qter	"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufv2 (MGI:1920150)			
chr18	9136752	9285984	18p11.22	18p11.22		610616	"ANKRD12, ANCO1, KIAA0874"	Ankyrin repeat domain-containing protein 12	ANKRD12	23253	ENSG00000101745			Ankrd12 (MGI:1914357)			
chr18	9334766	9402419	18p11.3-p11.2	18p11.22		605049	"TWSG1, TSG"	"Twisted gastrulation, Drosophila, homolog of"	TWSG1	57045	ENSG00000128791			Twsg1 (MGI:2137520)			
chr18	9475531	9538107	18p11	18p11.22		605801	"RALBP1, RLIP76"	RALA-binding protein 1	RALBP1	10928	ENSG00000017797			Ralbp1 (MGI:108466)			
chr18	9546790	9615272	18p11.22	18p11.22		604908	"PPP4R1, PP4R1"	"Protein phosphatase 4, regulatory subunit 1"	PPP4R1	9989	ENSG00000154845			Ppp4r1 (MGI:1917601)			
chr18	9708186	9862555	18p11.3	18p11.22		605694	RAB31	Ras-associated protein RAB31	RAB31	11031	ENSG00000168461			Rab31 (MGI:1914603)			
chr18	9885725	9888158	18p11.22	18p11.22		617790	"TXNDC2, SPTRX1"	Thioredoxin domain-containing protein 2	TXNDC2	84203	ENSG00000168454			Txndc2 (MGI:2389312)			
chr18	9913957	9960020	18p11.22	18p11.22		605703	"VAPA, VAP33"	Vesicle-associated membrane protein-associated protein A	VAPA	9218	ENSG00000101558			Vapa (MGI:1353561)			
chr18	10454627	10488700	18p11	18p11.22		607479	"APCDD1, HHS, HYPT1, HTS"	Adenomatosis polyposis coli down-regulated 1	APCDD1	147495	ENSG00000154856		"Hypotrichosis 1, 605389 (3), Autosomal dominant"	Apcdd1 (MGI:3513977)			
chr18	10525875	10552768	18p11.22	18p11.22		603216	NAPG	"N-ethylmaleimide-sensitive factor attachment protein, gamma"	NAPG	8774	ENSG00000134265			Napg (MGI:104561)			
chr18	10670236	11149584	18p11.22	18p11.22-p11.21		613629	"PIEZO2, FAM38B, DA5, DA3, MWKS, DAIPT"	PIEZO-type mechanosensitive ion channel component 2	PIEZO2	63895	ENSG00000154864	mutation identified in 1 MWKS patient	"Arthrogryposis, distal, type 3, 114300 (3), Autosomal dominant; Arthrogryposis, distal, type 5, 108145 (3), Autosomal dominant; Arthrogryposis, distal, with impaired proprioception and touch, 617146 (3), Autosomal recessive; ?Marden-Walker syndrome, 248700 (3), Autosomal dominant"	Piezo2 (MGI:1918781)			
chr18	11689014	11885684	18p11.21	18p11.21		139312	"GNAL, DYT25"	"Guanine nucleotide-binding protein, alpha-subunit, olfactory type"	GNAL	2774	ENSG00000141404		"Dystonia 25, 615073 (3), Autosomal dominant"	Gnal (MGI:95774)			
chr18	11851389	11854448	18p11	18p11.21		606486	"CHMP1B, C10orf2"	"CHMP family, member 1B"	CHMP1B	57132	ENSG00000255112			Chmp1b (MGI:1914314)			
chr18	11883470	11908796	18p11.2	18p11.21		611900	MPPE1	Metallophosphoesterase 1	MPPE1	65258	ENSG00000154889			Mppe1 (MGI:2661311)			
chr18	11981427	12030885	18p11.2	18p11.21		605922	IMPA2	Myo-inositol monophosphatase 2	IMPA2	3613	ENSG00000141401			Impa2 (MGI:2149728)			
chr18	12254318	12277594	18p11.21	18p11.21		604440	CIDEA	Cell death-inducing DFFA-like effector A	CIDEA	1149	ENSG00000176194			Cidea (MGI:1270845)			
chr18	12307668	12329825	18p11.21	18p11.21		615103	"TUBB6, FPVEPD"	"Tubulin, beta-6"	TUBB6	84617	ENSG00000176014	mutation identified in 1 FPVEPD family	"?Facial palsy, congenitla, with ptosis and velopharyngeal dysfunction, 617732 (3), Autosomal dominant"	Tubb6 (MGI:1915201)			
chr18	12328943	12377308	18p11	18p11.21		604581	"AFG3L2, SCA28, SPAX5"	ATPase family gene 3-like 2	AFG3L2	10939	ENSG00000141385		"Spastic ataxia 5, autosomal recessive, 614487 (3), Autosomal recessive; Spinocerebellar ataxia 28, 610246 (3), Autosomal dominant"	Afg3l2 (MGI:1916847)			
chr18	12407895	12432237	18p11.21	18p11.21		616545	"PRELID3A, SLMO1, C18orf43"	PRELI domain-containing protein 3A	PRELID3A	10650	ENSG00000141391			Prelid3a (MGI:2442865)			
chr18	12658738	12725739	18p11.21	18p11.21		609702	"PSMG2, TNFSF5IP1, HCCA3, CLAST3, PAC2"	"Proteasome (prosome, macropain) assembly chaperone 1"	PSMG2	56984	ENSG00000128789			Psmg2 (MGI:1922901)			
chr18	12785477	12884350	18p11.3-p11.2	18p11.21		176887	"PTPN2, PTPT"	"Protein tyrosine phosphatase, nonreceptor-type, 2"	PTPN2	5771	ENSG00000175354			Ptpn2 (MGI:97806)			
chr18	12947983	12987664	18p11.21	18p11.21		609263	"SEH1L, SEH1, SEC13L"	Seh1-like protein	SEH1L	81929	ENSG00000085415			Seh1l (MGI:1919374)			
chr18	12991300	13125052	18p11.21	18p11.21		616426	"CEP192, PPP1R62, KIAA1569"	"Centrosomal protein, 192kD"	CEP192	55125	ENSG00000101639			Cep192 (MGI:1918049)			
chr18	13217603	13652753	18p11.2	18p11.21		606571	C18orf1	Chromosome 18 open reading frame 1	LDLRAD4	753	ENSG00000168675			Ldlrad4 (MGI:1277150)			
chr18	13726644	13764555	18p11.23-p11.22	18p11.21		603514	"RNMT, MET"	RNA guanine-7-methyltransferase	RNMT	8731	ENSG00000101654			Rnmt (MGI:1915147)			
chr18	13825543	13826861	18p11.2	18p11.21		600042	MC5R	Melanocortin-5 receptor	MC5R	4161	ENSG00000176136			Mc5r (MGI:99420)			
chr18	13882041	13915706	18p11.2	18p11.21		607397	MC2R	Melanocortin-2 receptor (ACTH receptor)	MC2R	4158	ENSG00000185231		"Glucocorticoid deficiency, due to ACTH unresponsiveness, 202200 (3), Autosomal recessive"	Mc2r (MGI:96928)			
chr18	14748239	14855464	18p11.21	18p11.21		616565	ANKRD30B	Ankyrin repeat domain-containing protein 30B	ANKRD30B	374860	ENSG00000180777						
chr18	18500000	80373285	18q			601808	DEL18q	Chromosome 18q deletion syndrome					"Chromosome 18q deletion syndrome, 601808 (4), Autosomal dominant"				
chr18	18500000	80373285	18q			143850	OHDS	Orthostatic hypotensive disorder of Streeten		50948			"Orthostatic hypotensive disorder of Streeten, 143850 (2), Autosomal dominant"				
chr18	20949739	21111850	18q11.1	18q11.1		601702	ROCK1	RHO-associated coiled-coil-containing protein kinase 1	ROCK1	6093	ENSG00000067900			Rock1 (MGI:107927)			
chr18	21242224	21528502	18q11.1	18q11.1-q11.2		617782	"GREB1L, C18orf6, KIAA1772, RHDA3"	GREB1-like protein	GREB1L	80000	ENSG00000141449		"Renal hypodysplasia/aplasia 3, 617805 (3)"	Greb1l (MGI:3576497)			
chr18	21500000	39500000	18q11.2-q12.2			613930	APMR3	Alopecia-mental retardation syndrome 3		100653369		between D18S866 and D18S811	"Alopecia-mental retardation syndrome 3, 613930 (2), Autosomal recessive"				
chr18	21529280	21600735	18q11.2	18q11.2		609674	"ESCO1, ECO1, CTF, ESO1, EFO1, KIAA1911"	"Establishment of cohesion 1, S. cerevisiae, homolog of, 1"	ESCO1	114799	ENSG00000141446			Esco1 (MGI:1925055)			
chr18	21612268	21630246	18q11.2	18q11.2		601063	SNRPD1	Small nuclear ribonucleoprotein polypeptide D1	SNRPD1	6632	ENSG00000167088			Snrpd1 (MGI:98344)			
chr18	21650896	21704804	18q11.1	18q11.2		612197	"ABHD3, LABH3"	Abhydrolase domain-containing 3	ABHD3	171586	ENSG00000158201			Abhd3 (MGI:2147183)			
chr18	21740792	21870956	18q11.2	18q11.2		608677	"MIB1, MIB, DIP1, KIAA1323, LVNC7"	"Mindbomb, Drosophila, homolog of, 1"	MIB1	57534	ENSG00000101752		"Left ventricular noncompaction 7, 615092 (3), Autosomal dominant"	Mib1 (MGI:2443157)			
chr18	21825697	21825784	18q11.2	18q11.2		610254	MIR133A1	Micro RNA 133A1	MIR133A1	406922							
chr18	21829003	21829087	18q11.2	18q11.2		610252	MIR1-2	Micro RNA 1-2	MIR1-2	406905							
chr18	22169436	22202527	18q11.1-q11.2	18q11.2		601656	"GATA6, AVSD5, ASD9, PACHD"	GATA-binding protein-6	GATA6	2627	ENSG00000141448		"Atrial septal defect 9, 614475 (3), Autosomal dominant; Atrioventricular septal defect 5, 614474 (3), Autosomal dominant; Pancreatic agenesis and congenital heart defects, 600001 (3), Autosomal dominant; Persistent truncus arteriosus, 217095 (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant"	Gata6 (MGI:107516)			
chr18	22914120	23026485	18q11.2	18q11.2		604124	"RBBP8, RIM, SCKL2, JWDS"	Retinoblastoma-binding protein 8	RBBP8	5932	ENSG00000101773		"Jawad syndrome, 251255 (3), Autosomal recessive; Pancreatic carcinoma, somatic (3); Seckel syndrome 2, 606744 (3), Autosomal recessive"	Rbbp8 (MGI:2442995)			
chr18	23237251	23437968	18q11.2	18q11.2		615430	"TMEM241, C18orf45"	Transmembrane protein 241	TMEM241	85019	ENSG00000134490			Tmem241 (MGI:2442435)			
chr18	23452822	23483139	18q11.2	18q11.2		603579	"RIOK3, SUDD"	RIO kinase 3	RIOK3	8780	ENSG00000101782			Riok3 (MGI:1914128)			
chr18	23506183	23586616	18q11-q12	18q11.2		607623	"NPC1, NPC"	NPC1 gene	NPC1	4864	ENSG00000141458	some families not linked to 18; type D prob. allelic	"Niemann-Pick disease, type C1, 257220 (3), Autosomal recessive; Niemann-Pick disease, type D, 257220 (3), Autosomal recessive"	Npc1 (MGI:1097712)			
chr18	23689442	23955065	18q11.2	18q11.2		600805	"LAMA3, LOCS"	"Laminin, alpha-3 (nicein, 150kD; kalinin, 165kD; BM600, 150kD; epiligrin)"	LAMA3	3909	ENSG00000053747		"Epidermolysis bullosa, generalized atrophic benign, 226650 (3), Autosomal recessive; Epidermolysis bullosa, junctional, Herlitz type, 226700 (3), Autosomal recessive; Laryngoonychocutaneous syndrome, 245660 (3), Autosomal recessive"	Lama3 (MGI:99909)			
chr18	24138955	24161599	18q12.2	18q11.2		612135	"CABYR, FSP2"	Calcium-binding tyrosine phosphorylation-regulated protein	CABYR	26256	ENSG00000154040			Cabyr (MGI:1918382)			
chr18	24162044	24397881	18q11-q12	18q11.2		606730	"OSBPL1A, ORP1"	Oxysterol-binding protein-like protein 1A	OSBPL1A	114876	ENSG00000141447			Osbpl1a (MGI:1927551)			
chr18	24426644	24453530	18q11.2-q12.1	18q11.2		615319	IMPACT	Impact RWD domain protein	IMPACT	55364	ENSG00000154059			Impact (MGI:1098233)			
chr18	24460628	24479956	18q11.2	18q11.2		606792	"HRH4, HH4R"	Histamine receptor H4	HRH4	59340	ENSG00000134489			Hrh4 (MGI:2429635)			
chr18	25061923	25352249	18q11.2	18q11.2		610974	"ZNF521, EHZF, EVI3"	Zinc finger protein 521	ZNF521	25925	ENSG00000198795			Zfp521 (MGI:95459)			
chr18	26016252	26091216	18q11.2	18q11.2		600192	"SS18, SSXT, SYT"	"Synovial sarcoma translocation, chromosome 18"	SS18	6760	ENSG00000141380	5' SYST/3' SSRC in t(X;18)	"Sarcoma, synovial (1)"	Ss18 (MGI:107708)			
chr18	26133846	26193354	18q11.2	18q11.2		617841	"PSMA8, PSMA7L"	"Proteasome subunit, alpha-type, 8"	PSMA8	143471	ENSG00000154611			Psma8 (MGI:1920927)			
chr18	26226444	26391684	18q11.2	18q11.2		601689	"TAF4B, TAF2C2, TAFII105, SPGF13"	"TAF4b RNA polymerase II, TATA box-binding protein-associated factor, 105kD"	TAF4B	6875	ENSG00000141384	mutation identified in 1 SPGF13 family	"?Spermatogenic failure 13, 615841 (3), Autosomal recessive"	Taf4b (MGI:2152345)			
chr18	26454909	26657511	18q11.2	18q11.2		613420	"KCTD1, SENS"	Potassium channel tetramerization domain-containing 1	KCTD1	284252	ENSG00000134504		"Scalp-ear-nipple syndrome, 181270 (3), Autosomal dominant"	Kctd1 (MGI:1918269)			
chr18	26687620	26703637	18q11.2	18q11.2		617647	"PCAT18, LINC01092"	"Prostate cancer-associated transcript 18, noncoding"	PCAT18	728606							
chr18	26852037	26865802	18q11.2-q12.1	18q11.2		600308	"AQP4, MIWC"	Aquaporin-4	AQP4	361	ENSG00000171885			Aqp4 (MGI:107387)			
chr18	26908753	27185363	18q11.2	18q11.2		610191	"CHST9, GalNAc4ST2"	Carbohydrate sulfotransferase 9	CHST9	83539	ENSG00000154080			Chst9 (MGI:1918617)			
chr18	27932877	28177445	18q11.2	18q12.1		114020	"CDH2, NCAD"	"Cadherin 2 (cadherin, neuronal type; N-cadherin)"	CDH2	1000	ENSG00000170558			Cdh2 (MGI:88355)			
chr18	30989364	31042814	18q12.1	18q12.1		600271	"DSC3, DSC4"	Desmocollin-3	DSC3	1825	ENSG00000134762	mutation identified in 1 HYPTSV family	"?Hypotrichosis and recurrent skin vesicles, 613102 (3), Autosomal recessive"	Dsc3 (MGI:1194993)			
chr18	31065973	31102431	18q12.1	18q12.1		125645	"DSC2, DSC3, ARVD11"	Desmocollin-2	DSC2	1824	ENSG00000134755		"Arrhythmogenic right ventricular dysplasia 11, 610476 (3), Autosomal recessive, Autosomal dominant; Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair, 610476 (3), Autosomal recessive, Autosomal dominant"	Dsc2 (MGI:103221)			
chr18	31129235	31162855	18q12.1	18q12.1		125643	DSC1	Desmocollin-1	DSC1	1823	ENSG00000134765			Dsc1 (MGI:109173)			
chr18	31318088	31359245	18q12.1-q12.2	18q12.1		125670	"DSG1, PPKS1, SPPK1, EPKHE"	Desmoglein-1	DSG1	1828	ENSG00000134760	pemphigus foliaceous antigen	"Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, 615508 (3), Autosomal recessive; Keratosis palmoplantaris striata I, AD, 148700 (3), Autosomal dominant"	"Dsg1a,Dsg1b (MGI:94930,MGI:2664357)"			
chr18	31376776	31415790	18q12	18q12.1		607892	"DSG4, LAH, HYPT6"	Desmoglein 4	DSG4	147409	ENSG00000175065		"Hypotrichosis 6, 607903 (3), Autosomal recessive"	Dsg4 (MGI:2661061)			
chr18	31447768	31478711	18q12.1-q12.2	18q12.1		169615	DSG3	Desmoglein-3 (pemphigus vulgaris antigen)	DSG3	1830	ENSG00000134757			Dsg3 (MGI:99499)			
chr18	31498003	31549007	18q12.1-q12.2	18q12.1		125671	"DSG2, ARVD10, ARVC10, CMD1BB"	Desmoglein-2	DSG2	1829	ENSG00000046604		"Arrhythmogenic right ventricular dysplasia 10, 610193 (3), Autosomal dominant; Cardiomyopathy, dilated, 1BB, 612877 (3)"	Dsg2 (MGI:1196466)			
chr18	31591766	31599023	18q11.2-q12.1	18q12.1		176300	"TTR, PALB"	Transthyretin (prealbumin)	TTR	7276	ENSG00000118271		"Amyloidosis, hereditary, transthyretin-related, 105210 (3), Autosomal dominant; Carpal tunnel syndrome, familial, 115430 (3), Autosomal dominant; [Dystransthyretinemic hyperthyroxinemia], 145680 (3), Autosomal dominant"	Ttr (MGI:98865)			
chr18	31621035	31724669	18q11	18q12.1		604017	B4GALT6	"Beta-1,4-galactosyltransferase 6"	B4GALT6	9331	ENSG00000118276			B4galt6 (MGI:1928380)			
chr18	31759695	31760879	18q12.1	18q12.1		616153	"SLC25A52, MCART2"	"Solute carrier family 25, member 52"	SLC25A52	147407	ENSG00000141437						
chr18	31829172	31943127	18q12.1	18q12.1		614136	"TRAPPC8, KIAA1012"	"Trafficking protein particle complex, subunit 8"	TRAPPC8	22878	ENSG00000153339			Trappc8 (MGI:2443008)			
chr18	32018481	32090755	18q12.1	18q12.1		610432	"RNF125, TRAC1, TNORS"	RING finger protein 125	RNF125	54941	ENSG00000101695		"Tenorio syndrome, 616260 (3), Autosomal dominant"				
chr18	32091854	32131560	18q12.1	18q12.1		616319	"RNF138, NARF"	RING finger protein 138	RNF138	51444	ENSG00000134758			Rnf138 (MGI:1929211)			
chr18	32190023	32222606	18q12.2-q12.3	18q12.1		600389	MEP1B	"Meprin A, beta"	MEP1B	4225	ENSG00000141434			Mep1b (MGI:96964)			
chr18	32672672	32773010	18q12.1	18q12.1		613772	"KLHL14, PRINTOR, KIAA1384"	Kelch-like 14	KLHL14	57565	ENSG00000197705			Klhl14 (MGI:1921249)			
chr18	33578576	33751194	18q12.1	18q12.1		615115	"ASXL3, KIAA1713, BRPS"	Additional sex combs-like 3	ASXL3	80816	ENSG00000141431		"Bainbridge-Ropers syndrome, 615485 (3)"	Asxl3 (MGI:2685175)			
chr18	33851099	34224956	18q12.1	18q12.1		603577	"NOL4, NOLP"	Nucleolar protein 4	NOL4	8715	ENSG00000101746			Nol4 (MGI:2441684)			
chr18	34493289	34891843	18q12.1-q12.2	18q12.1		601239	"DTNA, D18S892E, DRP3, LVNC1"	"Dystobrevin, alpha (dystrophin-related protein 3)"	DTNA	1837	ENSG00000134769		"Left ventricular noncompaction 1, with or without congenital heart defects, 604169 (3), Autosomal dominant"	Dtna (MGI:106039)			
chr18	34976927	35143469	18q12	18q12.1-q12.2		605789	"MAPRE2, EB2, RP1, CSCSC2"	"Microtubule-associated protein, RP/EB family, member 2"	MAPRE2	10982	ENSG00000166974		"Symmetric circumferential skin creases, congenital, 2, 616734 (3), Autosomal dominant"				
chr18	35100000	45900000	18q12.2-q12.3			605293	OPA4	Optic atrophy 4	OPA4	58156			"Optic atrophy 4, 605293 (2)"				
chr18	35240703	35258432	18q12	18q12.2		609601	ZNF397	Zinc finger protein-397	ZNF397	84307	ENSG00000186812			Zfp397 (MGI:1916506)			
chr18	35290271	35310765	18q12	18q12.2		604754	"ZNFEB, ZNF271"	Epstein-Barr virus-induced zinc finger protein	ZNF271P	10778							
chr18	35332207	35344466	18q12	18q12.2		194534	ZNF24	Zinc finger protein-24 (KOX17)	ZNF24	7572	ENSG00000172466			Zfp24 (MGI:1929704)			
chr18	35366696	35377336	18q12	18q12.2		609600	ZNF396	Zinc finger protein-396	ZNF396	252884	ENSG00000186496						
chr18	35654568	35711833	18q12.1	18q12.2		602273	GALNT1	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 1	GALNT1	2589	ENSG00000141429			Galnt1 (MGI:894693)			
chr18	35904817	35904925	18q12.2	18q12.2		612698	"MIR187, MIRN187"	Micro RNA 187	MIR187	406963							
chr18	35982384	36067593	18q12	18q12.2		610347	"RPRD1A, P15RS, FLJ10656"	Regulation of nuclear pre-mRNA domain-containing protein 1A	RPRD1A	55197	ENSG00000141425			Rprd1a (MGI:2385066)			
chr18	36129873	36177930	18q12.2	18q12.2		616054	"ELP2, STATIP1, MRT58"	"Elongator acetyltransferase complex, subunit 2"	ELP2	55250	ENSG00000134759		"Mental retardation, autosomal recessive 58, 617270 (3), Autosomal recessive"	Elp2 (MGI:1889642)			
chr18	36187209	36268721	18q12.2	18q12.2		613274	"MOCOS, MCS, XAN2"	Molybdenum cofactor sulfurase	MOCOS	55034	ENSG00000075643		"Xanthinuria, type II, 603592 (3), Autosomal recessive"	Mocos (MGI:1915841)			
chr18	36297695	36780219	18q12.2	18q12.2		609691	"FHOD3, FHOS2, KIAA1695"	Formin homology-2 domain-containing protein 3	FHOD3	80206	ENSG00000134775			Fhod3 (MGI:1925847)			
chr18	36828816	37232126	18q12.2	18q12.2		616480	"KIAA1328, HINDERIN"	Hinderin	KIAA1328	57536	ENSG00000150477			AW554918 (MGI:2147376)			
chr18	37243039	37566036	18q12	18q12.2		612679	"CELF4, BRUNOL4"	"CUGbp- and ELAV-like family, member 4"	CELF4	56853	ENSG00000101489			Celf4 (MGI:1932407)			
chr18	39500000	45900000	18q12.3			614319	VUR6	Vesicoureteral reflux 6		100820763		closest marker rs1054986	"Vesicoureteral reflux 6, 614319 (2)"				
chr18	41955197	42084605	18q12.3	18q12.3		602609	PIK3C3	"Phosphatidylinositol 3-kinase, class 3"	PIK3C3	5289	ENSG00000078142			Pik3c3 (MGI:2445019)			
chr18	42743217	43115691	18q12.3	18q12.3		609592	"RIT2, RIN, ROC2"	Ric-like protein without CAAX motif 2	RIT2	6014	ENSG00000152214			Rit2 (MGI:108054)			
chr18	43267891	43277649	18q12.3	18q12.3		600103	SYT4	Synaptotagmin-4	SYT4	6860	ENSG00000132872			Syt4 (MGI:101759)			
chr18	44680071	45068509	18q12.31	18q12.3		611060	"SETBP1, KIAA0437, SEB, MRD29"	SET-binding protein 1	SETBP1	26040	ENSG00000152217	fused with NUP98 in ALL	"Mental retardation, autosomal dominant 29, 616078 (3), Autosomal dominant; Schinzel-Giedion midface retraction syndrome, 269150 (3), Autosomal dominant"	Setbp1 (MGI:1933199)			
chr18	45202957	45683685	18q12.1-q21.1	18q12.3		601611	"SLC14A2, UT2, UTR"	"Solute carrier family 14 (urea transporter), member 2"	SLC14A2	8170	ENSG00000132874			Slc14a2 (MGI:1351653)			
chr18	45724122	45752519	18q11-q12	18q12.3		613868	"SLC14A1, JK, UTE, UT1"	"Solute carrier family 14 (urea transporter), member 1 (Kidd blood group)"	SLC14A1	6563	ENSG00000141469	previous suggestion of chr.7 or chr.2	"[Blood group, Kidd], 111000 (3)"	Slc14a1 (MGI:1351654)			
chr18	45800585	45967338	18q12.3-q21.1	18q12.3-q21.1		615068	"EPG5, KIAA1632, HEEW1, VICIS"	"Ectopic P-granules autophagy protein 5, C. elegans, homolog of"	EPG5	57724	ENSG00000152223		"Vici syndrome, 242840 (3), Autosomal recessive"	Epg5 (MGI:1918673)			
chr18	45900000	63900000	18q21			606640	ALS3	Amyotrophic lateral sclerosis 3	ALS3	253			"Amyotrophic lateral sclerosis 3, 606640 (2), Autosomal dominant"				
chr18	45900000	63900000	18q21.1-q21.3			600624	"CORD1, CRD1"	"Cone rod dystrophy 1, autosomal dominant"	CORD1	1319			"Cone-rod retinal dystrophy-1, 600624 (2), Autosomal dominant"				
chr18	45900000	63900000	18q21			601941	IDDM6	Insulin-dependent diabetes mellitus-6	IDDM6	3405			"{Diabetes mellitus, insulin-dependent, 6}, 601941 (2)"				
chr18	45900000	63900000	18q21			182090	SSAV1	Simian sarcoma-associated virus-1/Gibbon ape leukemia virus		6739							
chr18	45983535	46072326	18q21.1	18q21.1		616046	"PSTPIP2, MAYP"	Proline/serine/threonine phosphatase-interacting protein 2	PSTPIP2	9050	ENSG00000152229			Pstpip2 (MGI:1335088)			
chr18	46084143	46104232	18q12-q21	18q21.1		164360	"ATP5A1, ATPM, ATP5A, ORM, MC5DN4, COXPD22"	"ATP synthase, H+ transporting (ATPase, mitochondrial)"	ATP5F1A	498	ENSG00000152234	"pseudogenes on chr. 2, chr. 9, and chr.16; mutation identified in 1 MC5DN4 family and 1 COXPD22 family"	"?Combined oxidative phosphorylation deficiency 22, 616045 (3), Autosomal recessive; ?Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3), Autosomal recessive"	Atp5a1 (MGI:88115)			
chr18	46104331	46128332	18q21.1	18q21.1		608775	"HAUS1, CCDC5, HEIC"	"HAUS augmin-like complex, subunit 1"	HAUS1	115106	ENSG00000152240	"pseudogenes on 5, 8, and X"		Haus1 (MGI:2385076)			
chr18	46476971	46657114	18q12-q21	18q21.1		613072	"LOXHD1, DFNB77"	Lipoxygenase homology domains-containing 1	LOXHD1	125336	ENSG00000167210		"Deafness, autosomal recessive 77, 613079 (3), Autosomal recessive"				
chr18	46679117	46757168	18q21.1	18q21.1		607162	SIAT8E	Sialyltransferase 8E	ST8SIA5	29906	ENSG00000101638			St8sia5 (MGI:109243)			
chr18	46917549	47104794	18q21.1	18q21.1		614697	KATNAL2	"Katanin, p60 subunit, A-like protein 2"	KATNAL2	83473	ENSG00000167216			Katnal2 (MGI:1924234)			
chr18	47155018	47176373	18q21.1	18q21.1		609382	"IER3IP1, MEDS"	Immediate-early response 3-interacting protein 1	IER3IP1	51124	ENSG00000134049		"Microcephaly, epilepsy, and diabetes syndrome, 614231 (3), Autosomal recessive"	Ier3ip1 (MGI:1913441)			
chr18	47206176	47249523	18q21.1	18q21.1		617138	"SKOR2, FUSSEL18, CORL2"	SKI family transcriptional corepressor 2	SKOR2	652991	ENSG00000215474			Skor2 (MGI:3645984)			
chr18	47833094	47931187	18q21	18q21.1		601366	"MADH2, JV18, SMAD2"	"Mothers against decapentaplegic, Drosophila, homolog of, 2"	SMAD2	4087	ENSG00000175387			Smad2 (MGI:108051)			
chr18	48026885	48412638	18q21	18q21.1		616591	"ZBTB7C, APM1"	Zinc finger- and BTB domain-containing protein 7C	ZBTB7C	201501	ENSG00000184828			Zbtb7c (MGI:2443302)			
chr18	48539055	48863216	18q21.1	18q21.1		613178	"KIAA0427, CTIF"	KIAA0427 gene	CTIF	9811	ENSG00000134030			Ctif (MGI:2685518)			
chr18	48919852	48950710	18q21.1	18q21.1		602932	"SMAD7, MADH7, CRCS3"	"Mothers against decapentaplegic, Drosophila, homolog of, 7"	SMAD7	4092	ENSG00000101665		"{Colorectal cancer, susceptibility to, 3}, 612229 (3)"	Smad7 (MGI:1100518)			
chr18	49041473	49460732	18q12-q21.1	18q21.1		607461	"DYM, FLJ90130, DMC, SMC"	Dymeclin	DYM	54808	ENSG00000141627		"Dyggve-Melchior-Clausen disease, 223800 (3), Autosomal recessive; Smith-McCort dysplasia, 607326 (3), Autosomal recessive"	Dym (MGI:1918480)			
chr18	49488480	49492564	18q	18q21.1		603661	RPL17	Ribosomal protein L17	RPL17	6139	ENSG00000265681			"Rpl17-ps8,Rpl17 (MGI:2448270,MGI:3802129)"			
chr18	49560698	49592907	18q21.1	18q21.1		603684	"LIPG, EL, EDL"	"Lipase G, endothelial"	LIPG	9388	ENSG00000101670			Lipg (MGI:1341803)			
chr18	49783503	49813880	18q21.1	18q21.1		604770	ACAA2	Acetyl-CoA acyltransferase 2	ACAA2	10449	ENSG00000167315			Acaa2 (MGI:1098623)			
chr18	49814022	49814442	18q21.1	18q21.1		615645	SCARNA17	Small Cajal body-specific RNA 17	SCARNA17	677769							
chr18	49822785	50195080	18q21	18q21.1		606540	"MYO5B, KIAA1119"	Myosin VB	MYO5B	4645	ENSG00000167306		"Microvillus inclusion disease, 251850 (3), Autosomal recessive"	Myo5b (MGI:106598)			
chr18	50227192	50266521	18q21.1	18q21.1		614759	"CCDC11, HTX6"	Coiled-coil domain-containing protein 11	CFAP53	220136	ENSG00000172361		"Heterotaxy, visceral, 6, autosomal recessive, 614779 (3), Autosomal recessive"	Cfap53 (MGI:1921703)			
chr18	50266881	50281773	18q21.1	18q21.1		156535	"MBD1, PCM1"	Methyl=CpG binding domain protein 1 (protein containing methyl-CpG binding domain 1)	MBD1	4152	ENSG00000141644			Mbd1 (MGI:1333811)			
chr18	50375021	50394167	18q21.1	18q21.1		616673	"SKA1, C18orf24"	"Spindle- and kinetochore-associated complex, subunit 1"	SKA1	220134	ENSG00000154839			Ska1 (MGI:1913718)			
chr18	50559771	50731825	18q12-q21	18q21.1-q21.2		176949	"MAPK4, PRKM4, ERK3"	Mitogen-activated protein kinase 4	MAPK4	5596	ENSG00000141639			Mapk4 (MGI:2444559)			
chr18	50700000	56200000	18q21.2			611014	HYT8	"Hypertension, essential, susceptibility to, 8"		100188321		associated with rs1941958 and rs1893379	"{Hypertension, essential, susceptibility to, 8}, 611014 (2)"				
chr18	50795119	50825412	18q21	18q21.2		608080	"MRO, B29"	Maestro	MRO	83876	ENSG00000134042			Mro (MGI:2152817)			
chr18	50878701	50949794	18q21	18q21.2		154270	ME2	"Malic enzyme, mitochondrial"	ME2	4200	ENSG00000082212	10cM distal to F13A; previously mapped to chr.6		Me2 (MGI:2147351)			
chr18	50968016	50988119	18q21	18q21.2		608079	"ELAC1, D29"	"Elac, E. coli, homolog of, 1"	ELAC1	55520	ENSG00000141642			Elac1 (MGI:1890495)			
chr18	51030212	51085041	18q21.1	18q21.2		600993	"SMAD4, MADH4, DPC4, JIP, MYHRS"	"Mothers against decapentaplegic, Drosophila, homolog of, 4"	SMAD4	4089	ENSG00000141646		"Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome, 175050 (3), Autosomal dominant; Myhre syndrome, 139210 (3), Autosomal dominant; Pancreatic cancer, somatic, 260350 (3); Polyposis, juvenile intestinal, 174900 (3), Autosomal dominant"	Smad4 (MGI:894293)			
chr18	51174549	51197680	18q21.2	18q21.2		611005	"MEX3C, RKHD2"	"Mex-3, C. elegans, homolog of, C"	MEX3C	51320	ENSG00000176624			Mex3c (MGI:2652843)			
chr18	52340171	53535902	18q21.3	18q21.2		120470	"DCC, MRMV1, HGPPS2"	Deleted in colorectal carcinoma	DCC	1630	ENSG00000187323		"Colorectal cancer, somatic, 114500 (3); Esophageal carcinoma, somatic, 133239 (3); Gaze palsy, familial horizontal, with progressive scoliosis, 2, 617542 (3), Autosomal recessive; Mirror movements 1 and/or agenesis of the corpus callosum, 157600 (3), Autosomal dominant"	Dcc (MGI:94869)			
chr18	54151600	54224787	18q21	18q21.2		603547	MBD2	Methyl-CpG-binding domain protein 2	MBD2	8932	ENSG00000134046			Mbd2 (MGI:1333813)			
chr18	54269478	54321265	18q21.1	18q21.2		605252	"POLI, RAD30B"	"Polymerase, DNA, iota"	POLI	11201	ENSG00000101751			Poli (MGI:1347081)			
chr18	54324591	54358461	18q21	18q21.2		607051	STARD6	Start domain-containing protein 6	STARD6	147323	ENSG00000174448			Stard6 (MGI:2156774)			
chr18	54357913	54382034	18q21	18q21.2		613258	"C18orf54, LAS2"	Chromosome 18 open reading frame 54	C18orf54	162681	ENSG00000166845			4930503L19Rik (MGI:1922045)			
chr18	54901508	54959538	18q21.2	18q21.2		616909	CCDC68	Coiled-coil domain-containing protein 68	CCDC68	80323	ENSG00000166510			Ccdc68 (MGI:3612676)			
chr18	55222330	55635992	18q21.2	18q21.2		602272	"TCF4, SEF2, ITF2, PTHS, FECD3"	Transcription factor-4 (immunoglobulin transcription factor-2)	TCF4	6925	ENSG00000196628		"Corneal dystrophy, Fuchs endothelial, 3, 613267 (3), Autosomal dominant; Pitt-Hopkins syndrome, 610954 (3), Autosomal dominant"	Tcf4 (MGI:98506)			
chr18	56200000	63900000	18q21.3			212200	CNSN	Carnosinemia (carnosinase)		8173			"Carnosinemia, 212200 (2), Autosomal recessive"				
chr18	56602821	56638688	18q21.31	18q21.31		603049	"TXNL1, TXNL"	Thioredoxin-like 1	TXNL1	9352	ENSG00000091164			Txnl1 (MGI:1860078)			
chr18	56651358	57029804	18q21.3	18q21.31		613473	"WDR7, TRAG, KIAA0541"	WD repeat-containing protein 7	WDR7	23335	ENSG00000091157			Wdr7 (MGI:1860197)			
chr18	57054558	57072118	18q21.2	18q21.31		615173	LINC-ROR	"Long intergenic noncoding RNA, regulator of reprogramming"	LINC-ROR	100885779							
chr18	57435684	57491297	18q21.1-q21.2	18q21.31		604894	"ONECUT2, OC2"	"One cut domain, family member 2"	ONECUT2	9480	ENSG00000119547			Onecut2 (MGI:1891408)			
chr18	57544840	57586736	18q21.3	18q21.31		612386	"FECH, FCE"	Ferrochelatase	FECH	2235	ENSG00000066926		"Protoporphyria, erythropoietic, autosomal recessive, 177000 (3), Autosomal recessive"	Fech (MGI:95513)			
chr18	57600655	57621944	18q21.1-q21.3	18q21.31		108410	"NARS, ASNRS"	Asparaginyl-tRNA synthetase	NARS	4677	ENSG00000134440			Nars (MGI:1917473)			
chr18	57646425	57803821	18q21	18q21.31		602397	"ATP8B1, FIC1, BRIC, PFIC1, ICP1"	"ATPase, class I, type 8B, member 1"	ATP8B1	5205	ENSG00000081923		"Cholestasis, benign recurrent intrahepatic, 243300 (3), Autosomal recessive; Cholestasis, intrahepatic, of pregnancy, 1, 147480 (3), Autosomal dominant; Cholestasis, progressive familial intrahepatic 1, 211600 (3), Autosomal recessive"	Atp8b1 (MGI:1859665)			
chr18	58044233	58401539	18q21	18q21.31		606384	"NEDD4L, KIAA0439, RSP5, PVNH7"	Ubiquitin protein ligase NEDD4-like	NEDD4L	23327	ENSG00000049759		"Periventricular nodular heterotopia 7, 617201 (3), Autosomal dominant"	Nedd4l (MGI:1933754)			
chr18	58451073	58451157	18q21	18q21.31		609582	"MIR122A, MIRN122A"	Micro RNA 122A	MIR122	406906							
chr18	58671385	58753805	18q21	18q21.32		604860	"MALT1, MLT, IMD12"	Mucosa-associated lymphoid tissue lymphoma translocation gene 1	MALT1	10892	ENSG00000172175	fused with API2 in MALT lymphoma	"Immunodeficiency 12, 615468 (3), Autosomal recessive"	Malt1 (MGI:2445027)			
chr18	59219187	59230773	18q21	18q21.32		137260	GRP	Gastrin-releasing peptide	GRP	2922	ENSG00000134443	mammalian equivalent of bombesin		Grp (MGI:95833)			
chr18	59267034	59273392	18q21.3	18q21.32		601881	"RAX, RX, MCOP3"	Retina and anterior neural fold homeobox gene	RAX	30062	ENSG00000134438		"Microphthalmia, isolated 3, 611038 (3), Autosomal recessive"	Rax (MGI:109632)			
chr18	59327822	59359275	18q21.3-q22	18q21.32		601567	"LMAN1, ERGIC53, F5F8D, MCFD1"	"Lectin, mannose-binding, 1"	LMAN1	3998	ENSG00000074695		"Combined factor V and VIII deficiency, 227300 (3), Autosomal recessive"	Lman1 (MGI:1917611)			
chr18	59430938	59698180	18q21.32	18q21.32		612753	"CCBE1, KIAA1983, HKLLS1"	Collagen and calcium-binding EGF domain-containing protein 1	CCBE1	147372	ENSG00000183287		"Hennekam lymphangiectasia-lymphedema syndrome 1, 235510 (3), Autosomal recessive"	Ccbe1 (MGI:2445053)			
chr18	59899959	59904305	18q21.32	18q21.32		604959	"PMAIP1, APR, NOXA"	Phorbol-12-myristate-13-acetate-induced protein 1	PMAIP1	5366	ENSG00000141682						
chr18	60371330	60372767	18q22	18q21.32		155541	MC4R	Melanocortin-4 receptor	MC4R	4160	ENSG00000166603		"Obesity, autosomal dominant, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial"	Mc4r (MGI:99457)			
chr18	61333581	61555772	18q22-q23	18q21.33		605807	CDH20	Cadherin 20	CDH20	28316	ENSG00000101542			Cdh20 (MGI:1346069)			
chr18	61808066	61894419	18q21.33	18q21.33		616512	RNF152	Ring finger protein 152	RNF152	220441	ENSG00000176641			Rnf152 (MGI:2443787)			
chr18	62044223	62187117	18q21.33	18q21.33		606097	"PIGN, MCAHS1"	"Phosphatidylinositol glycan, class N"	PIGN	23556	ENSG00000197563		"Multiple congenital anomalies-hypotonia-seizures syndrome 1, 614080 (3), Autosomal recessive"	Pign (MGI:1351629)			
chr18	62325286	62388095	18q22.1	18q21.33		603499	"TNFRSF11A, RANK, ODFR, FEO, OPTB7, PDB2"	"Tumor necrosis factor receptor superfamily, member 11A"	TNFRSF11A	8792	ENSG00000141655		"Osteolysis, familial expansile, 174810 (3), Autosomal dominant; Osteopetrosis, autosomal recessive 7, 612301 (3); {Paget disease of bone 2, early-onset}, 602080 (3), Autosomal dominant"	Tnfrsf11a (MGI:1314891)			
chr18	62715438	62980442	18q21.33	18q21.33		609396	"PHLPP1, SCOP, KIAA0606"	PH domain and leucine-rich repeat protein phosphatase	PHLPP1	23239	ENSG00000081913			Phlpp1 (MGI:2138327)			
chr18	63123345	63320279	18q21.3	18q21.33		151430	BCL2	B-cell CLL/lymphoma-2	BCL2	596	ENSG00000171791	most frequent hematologic malignancy t(14;18)(q32;q21)	"Leukemia/lymphoma, B-cell, 2 (3)"	Bcl2 (MGI:88138)			
chr18	63327735	63367272	18q21.3	18q21.33		136440	"KDSR, FVT1, EKVP4"	3-ketodihydrosphingosine reductase	KDSR	2531	ENSG00000119537	~10kb 5' to BCL2	"Erythrokeratodermia variabilis et progressiva 4, 617526 (3), Autosomal recessive"	Kdsr (MGI:1918000)			
chr18	63389189	63422518	18q21.3	18q21.33		609983	"VPS4B, SKD1"	"Vacuolar protein sorting 4, yeast, homolog of, B"	VPS4B	9525	ENSG00000119541			Vps4b (MGI:1100499)			
chr18	63476910	63505084	18q21.3	18q21.33		154790	"PI5, SERPINB5"	Protease inhibitor 5 (maspin)	SERPINB5	5268	ENSG00000206075	in cluster of serpins		Serpinb5 (MGI:109579)			
chr18	63519163	63569328	18q21.3	18q21.33		615662	SERPINB12	"Serpin peptidase inhibitor, clade (ovalbumin), member 12"	SERPINB12	89777	ENSG00000166634			Serpinb12 (MGI:1919119)			
chr18	63586653	63599198	18q21.3	18q21.33		604445	"SERPINB13, PI13, HURPIN"	Protease inhibitor 13	SERPINB13	5275	ENSG00000197641			Serpinb13 (MGI:3042250)			
chr18	63637258	63644318	18q21.3	18q21.33		600518	"SERPINB4, SCCA2"	"Serpin peptidase inhibitor, clade B (ovalbumin), member 4 (squamous cell carcinoma antigen 2)"	SERPINB4	6318	ENSG00000206073			Serpinb3a (MGI:3573933)			
chr18	63655196	63661962	18q21.3	18q21.33		600517	"SERPINB3, SCCA1"	"Serpin peptidase inhibitor, clade B (ovalbumin), member 3 (squamous cell carcinoma antigen 1)"	SERPINB3	6317	ENSG00000057149			Serpinb3d (MGI:2683295)			
chr18	63702303	63723892	18q21.3	18q21.33		615682	SERPINB11	"Serpin peptidase inhibitor, clade B (ovalbumin), member 11"	SERPINB11	89778	ENSG00000206072			Serpinb11 (MGI:1914207)			
chr18	63753046	63805375	18q21.3	18q21.33		603357	"SERPINB7, MEGSIN, PPKN"	"Serpin peptidase inhibitor, clade B (ovalbumin), member 7"	SERPINB7	8710	ENSG00000166396		"Palmoplantar keratoderma, Nagashima type, 615598 (3), Autosomal recessive"	Serpinb7 (MGI:2151053)			
chr18	63887704	63903889	18q21.3	18q21.3-q22.1		173390	"SERPINB2, PAI2, PLANH2"	"Serpin peptidase inhibitor, clade B (ovalbumin), member 2 (Plasminogen activator inhibitor, type II (arginine-serpin))"	SERPINB2	5055	ENSG00000197632	600kb telomeric to BCL2		Serpinb2 (MGI:97609)			
chr18	63900000	75400000	18q22			609334	"DUP18pDEL18q, DUP18qDEL18p"	Chromosome 18 pericentric inversion					"Chromosome 18 pericentric inversion, 609334 (4)"				
chr18	63900000	75400000	18q22.1-q22.3			602401	ECTD8	"Ectodermal dysplasia 8, hair/tooth/nail type"		101101768		between D18S857 and D18S815	"Ectodermal dysplasia 8, hair/tooth/nail type, 602401 (2), Autosomal recessive"				
chr18	63907968	63936110	18q21.3	18q22.1		602058	"SERPINB10, PI10"	"Protease inhibitor 10, ovalbumin type (bomapin)"	SERPINB10	5273	ENSG00000242550			Serpinb10 (MGI:2138648)			
chr18	63949258	63969328	18q21.3	18q22.1		612086	HMSD	"Minor histocompatibility antigen, serpin domain-containing"	HMSD	284293	ENSG00000221887						
chr18	63970027	64019778	18q21.3	18q22.1		601697	"SERPINB8, PI8, CAP2, PSS5"	"Serpin family B, member 8"	SERPINB8	5271	ENSG00000166401		"Peeling skin syndrome 5, 617115 (3), Autosomal recessive"	Serpinb8 (MGI:894657)			
chr18	64080008	64149025	18q22.1	18q22.1		617489	LINC00305	Long intergenic noncoding RNA 305	LINC00305	221241							
chr18	65750251	65885135	18q22-q23	18q22.1		605806	CDH7	Cadherin-7	CDH7	1005	ENSG00000081138			Cdh7 (MGI:2442792)			
chr18	66501186	66604240	18q22-q23	18q22.1		603016	"CDH19, CDH7"	Cadherin 19	CDH19	28513	ENSG00000071991			Cdh19 (MGI:3588198)			
chr18	67506581	67516729	18q21-q22	18q22.1		611125	"DSEL, C18orf4, NCAG1"	Dermatan sulfate epimerase-like	DSEL	92126	ENSG00000171451			Dsel (MGI:2442948)			
chr18	68673687	68715172	18q22.1	18q22.1		616102	"TMX3, TXNDC10, KIAA1830"	Thioredoxin-related transmembrane protein 3	TMX3	54495	ENSG00000166479			Tmx3 (MGI:2442418)			
chr18	69860227	69962085	18q22.3	18q22.2		605397	"DNAM1, CD226"	DNAX accessory molecule 1	CD226	10666	ENSG00000150637			Cd226 (MGI:3039602)			
chr18	70003803	70205725	18q22.2	18q22.2		610436	"RTTN, MSSP"	Rotatin	RTTN	25914	ENSG00000176225		"Microcephaly, short stature, and polymicrogyria with seizures, 614833 (3), Autosomal recessive"	Rttn (MGI:2179288)			
chr18	70288900	70330198	18q21.1	18q22.2		605118	"SOCS6, SSI4, STAT4, CIS4"	Suppressor of cytokine signaling 6	SOCS6	9306	ENSG00000170677			Socs6 (MGI:1924885)			
chr18	72533719	72638484	18q22.3	18q22.3		600433	CBLN2	Cerebellin 2 precursor	CBLN2	147381	ENSG00000141668			Cbln2 (MGI:88282)			
chr18	72742313	72867671	18q22-q23	18q22.3		607973	"NETO1, BCTL1"	Neuropilin and tolloid like 1	NETO1	81832	ENSG00000166342			Neto1 (MGI:2180216)			
chr18	74073342	74147864	18q22.3	18q22.3		609093	"FBXO15, FBX15"	F-box only protein 15	FBXO15	201456	ENSG00000141665			Fbxo15 (MGI:1354755)			
chr18	74148510	74158968	18q22.3	18q22.3		615180	"TIMM21, TIM21"	"Translocase of inner mitochondrial membrane 21, yeast, homolog of"	TIMM21	29090	ENSG00000075336			Timm21 (MGI:1920595)			
chr18	74253291	74292015	18q23	18q22.3		613218	"CYB5A, MCB5"	Cytochrome b5	CYB5A	1528	ENSG00000166347	"pseudogenes on X, 14q, 20p; mutation identified in 1 MET5 patient"	"?Methemoglobinemia, type IV, 250790 (3), Autosomal recessive"	Cyb5a (MGI:1926952)			
chr18	74435727	74464645	18q22.3	18q22.3		614544	FAM69C	"Family with sequence similarity 69, member C"	FAM69C	125704	ENSG00000187773			Fam69c (MGI:3041188)			
chr18	74496264	74523453	18q23	18q22.3		169800	PEPA	Peptidase A	CNDP2	55748	ENSG00000133313			Cndp2 (MGI:1913304)			
chr18	74534456	74585024	18q22.3	18q22.3		609064	"CNDP1, CN1"	Carnosine dipeptidase 1	CNDP1	84735	ENSG00000150656			Cndp1 (MGI:2451097)			
chr18	74590474	75065671	18q22.3	18q22.3		615894	ZNF407	Zinc finger protein 407	ZNF407	55628	ENSG00000215421			Zfp407 (MGI:2685179)			
chr18	75210754	75289949	18q22.3	18q22.3		614427	"TSHZ1, TSH1, CAA"	Teashirt zinc finger homeobox 1	TSHZ1	10194	ENSG00000179981		"Aural atresia, congenital, 607842 (3), Autosomal dominant"	Tshz1 (MGI:1346031)			
chr18	76357681	76495254	18q23	18q23		615114	"ZNF516, KIAA0222"	Zinc finger protein 516	ZNF516	9658	ENSG00000101493			Zfp516 (MGI:2443957)			
chr18	76822549	76970731	18q22-q23	18q23		604760	ZNF236	Zinc finger protein-236	ZNF236	7776	ENSG00000130856			Zfp236 (MGI:1926950)			
chr18	76978832	77133707	18q22-qter	18q23		159430	MBP	Myelin basic protein	MBP	4155	ENSG00000197971	"defective in ""shiverer,"" neurologic mutant in mouse"		Mbp (MGI:96925)			
chr18	77250051	77270141	18q23	18q23		600377	"GALR1, GALNR1, GALNR"	Galanin receptor 1	GALR1	2587	ENSG00000166573			Galr1 (MGI:1096364)			
chr18	78980274	78998968	18q23	18q23		605079	SALL3	Sal-like 3	SALL3	27164	ENSG00000256463			Sall3 (MGI:109295)			
chr18	79069274	79378390	18q22.3-qter	18q23		614446	ATP9B	"ATPase, class II, type 9B"	ATP9B	374868	ENSG00000166377			Atp9b (MGI:1354757)			
chr18	79395771	79529322	18q23	18q23		600489	NFATC1	"Nuclear factor of activated T cells, cytoplasmic, calcineurin-dependent 1"	NFATC1	4772	ENSG00000131196			Nfatc1 (MGI:102469)			
chr18	79679800	79754509	18q23	18q23		604927	"CTDP1, FCP1, CCFDN"	"C-terminal domain of RNA polymerase II subunit A, phosphatase of, subunit 1"	CTDP1	9150	ENSG00000060069		"Congenital cataracts, facial dysmorphism, and neuropathy, 604168 (3), Autosomal recessive"	Ctdp1 (MGI:1926953)			
chr18	79972866	80033934	18q23	18q23		611595	"TXNL4A, DIM1, BMKS"	Thioredoxin-like 4A	TXNL4A	10907	ENSG00000141759		"Burn-McKeown syndrome, 608572 (3), Autosomal recessive"	Txnl4a (MGI:1351613)			
chr18	80109030	80140345	18q23	18q23		617422	"ADNP2, KIAA0863"	Activity-dependent neuroprotector homeobox 2	ADNP2	22850	ENSG00000101544			Adnp2 (MGI:2448562)			
chr18	80157231	80247513	18q23	18q23		608976	PARD6G	"partitioning-defective protein 6, C. elegans, homolog of"	PARD6G	84552	ENSG00000178184			Pard6g (MGI:2135606)			
chr19	0	12600000	19p13.3-p13.2			108725	"ATHS, ALP"	Atherosclerosis susceptibility (lipoprotein associated)	ATHS	470		closely linked to LDLR; may be LDLR	"{Atherosclerosis, susceptibility to}, 108725 (2), Autosomal dominant"				
chr19	0	58617616	19pter-q13			120050	CXB3S	Coxsackie virus B3 sensitivity	CXB3S	1526							
chr19	0	26200000	19p			600209	EXT3	"Exostoses, multiple, 3"	EXT3	2133			"Exostoses, multiple, type 3, 600209 (2), Autosomal dominant"				
chr19	0	6900000	19p13.3			602477	2-Feb	"Febrile seizures, familial, 2"	2-Feb	2234			"Febrile seizures, familial, 2, 602477 (2), Autosomal dominant"				
chr19	0	19900000	19pter-p13.1			614233	"FPH1, MUH, HPP"	"Hyperpigmentation, familial progressive, 1"					"Hyperpigmentation, familial progressive, 1, 614233 (2)"				
chr19	0	19900000	19p13			606674	IBD6	Inflammatory bowel disease 6	IBD6	50942			"{Inflammatory bowel disease 6}, 606674 (2)"				
chr19	0	6900000	19p13.3			181800	"IS1, AIS"	Adolescent idiopathic scoliosis		260402			"Scoliosis, idiopathic 1, 181800 (2), Autosomal dominant"				
chr19	0	6900000	19p13.3			605305	"KIR2DL5A, KIR2DL5"	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A"	KIR2DL5A	57292							
chr19	0	6900000	19p13.3			601846	MDRV	Muscular dystrophy with rimmed vacuoles	MDRV	4195			"Muscular dystrophy with rimmed vacuoles, 601846 (2), Autosomal dominant"				
chr19	0	19900000	19p13			607508	MGR5	"Migraine with or without aura, susceptibility to, 5"		387576			"{Migraine with or without aura, susceptibility to, 5}, 607508 (2), Autosomal dominant"				
chr19	0	19900000	19p13			615830	PPNAD4	"Pigmented nodular adrenocortical disease, primary, 4"				duplication of 294kb to 2.7Mb on 19p13	"Pigmented nodular adrenocortical disease, primary, 4, 615830 (4), Autosomal dominant"				
chr19	0	19900000	19p13			605364	PSORS6	Psoriasis susceptibility 6	PSORS6	63869			"{Psoriasis susceptibility 6}, 605364 (2)"				
chr19	281039	291434	19p13.3	19p13.3		607126	"PLPP2, PPAP2C"	Phospholipid phosphatase 2	PLPP2	8612	ENSG00000141934			Plpp2 (MGI:1354945)			
chr19	362056	376692	19p13.3	19p13.3		609503	THEG	"Testicular haploid expressed gene, mouse, homolog of"	THEG	51298	ENSG00000105549			Theg (MGI:1338756)			
chr19	405434	409169	19p13.3	19p13.3		610336	"C2CD4C, NLF3, KIAA1957"	C2 calcium-dependent domain containing 4C	C2CD4C	126567	ENSG00000183186			C2cd4c (MGI:2685084)			
chr19	416582	461010	19p13.3	19p13.3		605217	"SHC2, SHCB, SCK"	SHC transforming protein 2	SHC2	25759	ENSG00000129946			Shc2 (MGI:106180)			
chr19	496489	505342	19p13.3	19p13.3		102670	MACAM1	Mucosal addressin cell adhesion molecule-1	MADCAM1	8174	ENSG00000099866						
chr19	531719	542087	19p13.3	19p13.3		116948	CDC34	Cell division cycle 34	CDC34	997	ENSG00000099804			Cdc34 (MGI:102657)			
chr19	544033	549919	19p13.3	19p13.3		600311	GZMM	Granzyme M (lymphocyte met-ase 1)	GZMM	3004	ENSG00000197540			Gzmm (MGI:99549)			
chr19	571276	583492	19p13.3	19p13.3		109480	BSG	Basigin (blood group OK)	BSG	682	ENSG00000172270		"[Blood group, OK], 111380 (3)"	Bsg (MGI:88208)			
chr19	589892	617158	19p13.3	19p13.3		602781	"HCN2, BCNG2"	Hyperpolarization-activated cyclic nucleotide-gated potassium channel 2	HCN2	610	ENSG00000099822			Hcn2 (MGI:1298210)			
chr19	617220	633567	19p13.3	19p13.3		601778	"POLRMT, APOLMT"	Polymerase (RNA) mitochondrial (DNA directed)	POLRMT	5442	ENSG00000099821			Polrmt (MGI:1915843)			
chr19	639894	643702	19p13.3	19p13.3		605831	FGF22	Fibroblast growth factor 22	FGF22	27006	ENSG00000070388			Fgf22 (MGI:1914362)			
chr19	647525	663232	19p13.3	19p13.3		615177	RNF126	RING finger protein 126	RNF126	55658	ENSG00000070423			Rnf126 (MGI:1917544)			
chr19	676388	683391	19p13	19p13.3		605343	"FSTL3, FLRG"	Follistatin-like 3	FSTL3	10272	ENSG00000070404			Fstl3 (MGI:1890391)			
chr19	708952	748329	19p13.3	19p13.3		608134	"PALM, KIAA0270"	Paralemmin	PALM	5064	ENSG00000099864			Palm (MGI:1261814)			
chr19	748412	764318	19p13.3	19p13.3		615289	"MISP, C19orf21"	Mitotic spindle-positioning protein	MISP	126353	ENSG00000099812			Misp (MGI:1926156)			
chr19	797391	812326	19p13.3	19p13.3		600693	"PTBP1, PTB, HNRNPI"	Polypyrimidine tract-binding protein 1	PTBP1	5725	ENSG00000011304	pseudogene on chr. 14		Ptbp1 (MGI:97791)			
chr19	810965	824243	19p13.3	19p13.3		610391	"PLPPR3, LPPR3, LPR3, PRG2"	Phospholipid phosphatase-related protein 3	PLPPR3	79948	ENSG00000129951			Plppr3 (MGI:2388640)			
chr19	827825	832017	19p13.3	19p13.3		162815	"AZU1, CAP37"	Azurocidin-1 (cationic antimicrobial protein-37)	AZU1	566	ENSG00000172232	5\(rm-AZU1-8kb-PR3-3kb-ELAN-3'					
chr19	840964	848174	19p13.3	19p13.3		177020	"PRTN3, AGP7"	"Proteinase-3 (serine proteinase, neutrophil, Wegener granulomatosis autoantigen)"	PRTN3	5657	ENSG00000196415			Prtn3 (MGI:893580)			
chr19	850996	856249	19p13.3	19p13.3		130130	"ELANE, ELA2, SCN1"	"Elastase, neutrophil-expressed"	ELANE	1991	ENSG00000197561		"Neutropenia, cyclic, 162800 (3), Autosomal dominant; Neutropenia, severe congenital 1, autosomal dominant, 202700 (3), Autosomal dominant"	Elane (MGI:2679229)			
chr19	859658	863568	19p13.3	19p13.3		134350	"CFD, ADN"	Complement factor D	CFD	1675	ENSG00000197766		"Complement factor D deficiency, 613912 (3), Autosomal recessive"	Cfd (MGI:87931)			
chr19	916692	921014	19p13.3	19p13.3		604161	"KISS1R, GPR54, HH8, CPPB1"	KISS1 receptor	KISS1R	84634	ENSG00000116014	mutation identified in 1 CPPB1 patient	"Hypogonadotropic hypogonadism 8 with or without anosmia, 614837 (3), Autosomal recessive; ?Precocious puberty, central, 1, 176400 (3), Autosomal dominant"	Kiss1r (MGI:2148793)			
chr19	925732	975933	19p13.3	19p13.3		603265	DRIL1	"Dead ringer, Drosophila, homolog-like 1"	ARID3A	1820	ENSG00000116017			Arid3a (MGI:1328360)			
chr19	1009650	1021141	19p13.3	19p13.3		611011	"TMEM259, C19orf6"	Transmembrane protein 259 (membralin)	TMEM259	91304	ENSG00000182087			Tmem259 (MGI:2177957)			
chr19	1026274	1039067	19p13.3	19p13.3		602373	CNN2	Calonin 2	CNN2	1265	ENSG00000064666	previously assigned to 21q11.1		Cnn2 (MGI:105093)			
chr19	1040102	1065571	19p13.3	19p13.3		605414	"ABCA7, ABCX, AD9"	"ATP-binding cassette, subfamily A, member 7"	ABCA7	10347	ENSG00000064687		"{Alzheimer disease 9, susceptibility to}, 608907 (3), Autosomal dominant"	Abca7 (MGI:1351646)			
chr19	1065922	1087830	19p13.3	19p13.3		601155	"HMHA1, HLA-HA1, KIAA0223"	Minor histocompatibility antigen HA-1	ARHGAP45	23526	ENSG00000180448			Arhgap45 (MGI:1917969)			
chr19	1086578	1095391	19p13.3	19p13.3		180664	POLR2E	"Polymerase (RNA) II (DNA directed) polypeptide E, 25kD"	POLR2E	5434	ENSG00000099817			Polr2e (MGI:1913670)			
chr19	1103925	1106788	19p13.3	19p13.3		138322	"GPX4, SMDS"	Glutathione peroxidase-4 (phospholipid hydroperoxidase)	GPX4	2879	ENSG00000167468		"Spondylometaphyseal dysplasia, Sedaghatian type, 250220 (3), Autosomal recessive"	Gpx4 (MGI:104767)			
chr19	1107633	1174282	19p13.3	19p13.3		615729	"SBNO2, KIAA0963"	"Strawberry notch, Drosophila, homolog of, 2"	SBNO2	22904	ENSG00000064932			Sbno2 (MGI:2448490)			
chr19	1205798	1228434	19p13.3	19p13.3		602216	"STK11, PJS, LKB1"	Serine/threonine protein kinase-11	STK11	6794	ENSG00000118046		"Melanoma, malignant, somatic (3); Pancreatic cancer, 260350 (3), Autosomal dominant, Somatic mutation, Multifactorial; Peutz-Jeghers syndrome, 175200 (3), Autosomal dominant; Testicular tumor, somatic, 273300 (3)"	Stk11 (MGI:1341870)			
chr19	1241749	1244824	19p13.3	19p13.3		603150	ATP5D	"ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit"	ATP5F1D	513	ENSG00000099624			Atp5d (MGI:1913293)			
chr19	1248551	1259142	19p13.3	19p13.3		606700	MIDN	"Midnolin, mouse, homolog of"	MIDN	90007	ENSG00000167470			Midn (MGI:1890222)			
chr19	1269265	1274809	19p13.3	19p13.3		602649	CIRBP	Cold-inducible RNA-binding protein	CIRBP	1153	ENSG00000099622			Cirbp (MGI:893588)			
chr19	1282816	1301430	19p13.3	19p13.3		602756	"EFNA2, EPLG6, LERK6"	Ephrin A2	EFNA2	1943	ENSG00000099617			Efna2 (MGI:102707)			
chr19	1383883	1395588	19p13	19p13.3		601825	"NDUFS7, PSST"	"NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kD (NADH-coenzyme Q reductase)"	NDUFS7	374291	ENSG00000115286		"Leigh syndrome, 256000 (3), Autosomal recessive, Mitochondrial"	Ndufs7 (MGI:1922656)			
chr19	1397025	1401569	19p13.3	19p13.3		601240	"GAMT, CCDS2"	Guanidinoacetate methyltransferase	GAMT	2593	ENSG00000130005		"Cerebral creatine deficiency syndrome 2, 612736 (3), Autosomal recessive"	Gamt (MGI:1098221)			
chr19	1438363	1440496	19p	19p13.3		180535	"RPS15, RIG"	Ribosomal protein S15	RPS15	6209	ENSG00000115268			Rps15 (MGI:98117)			
chr19	1446267	1473243	19p13.3	19p13.3		612034	"APC2, APCL, SOTOS3"	APC2 gene	APC2	10297	ENSG00000115266	mutation identified in 1 SOTOS3 family	"?Sotos syndrome 3, 617169 (3), Autosomal recessive"	Apc2 (MGI:1346052)			
chr19	1481427	1490873	19p13.3	19p13.3		600487	PCSK4	Proprotein convertase subtilisin/kexin type 4	PCSK4	54760	ENSG00000115257			Pcsk4 (MGI:97514)			
chr19	1491004	1497926	19p13.3	19p13.3		609346	"REEP6, DP1L1, TB2L1, C19orf32, RP77"	Receptor expression-enhancing protein 6	REEP6	92840	ENSG00000115255		"Retinitis pigmentosa 77, 617304 (3), Autosomal recessive"	Reep6 (MGI:1917585)			
chr19	1554668	1568057	19p13.3	19p13.3		611009	"MEX3D, RKHD1, TINO, KIAA2031"	"Mex-3, C. elegans, homolog of, D"	MEX3D	399664	ENSG00000181588			Mex3d (MGI:2681847)			
chr19	1576670	1592760	19p13.3	19p13.3		603573	MBD3	Methyl-CpG-binding domain protein 3	MBD3	53615	ENSG00000071655			Mbd3 (MGI:1333812)			
chr19	1597154	1605483	19p13.3	19p13.3		609711	UQCR	"Ubiquinol-cytochrome c reductase, 6.4kD subunit"	UQCR11	10975	ENSG00000127540			Uqcr11 (MGI:1913844)			
chr19	1609283	1652545	19p13.3	19p13.3		147141	"TCF3, E2A, AGM8"	Transcription factor-3 (E2A immunoglobulin enhancer-binding factors E12/E47)	TCF3	6929	ENSG00000071564		"Agammaglobulinemia 8, autosomal dominant, 616941 (3), Autosomal dominant"	Tcf3 (MGI:98510)			
chr19	1753662	1775444	19p13.3	19p13.3		611294	"ONECUT3, OC3"	One cut homeobox 3	ONECUT3	390874	ENSG00000205922						
chr19	1782067	1812275	19p13.3	19p13.3		605866	"ATP8B3, ATPIK"	"ATPase, class I, type 8B, member 3"	ATP8B3	148229	ENSG00000130270			Atp8b3 (MGI:1914581)			
chr19	1815245	1848682	19p13.3	19p13.3		609614	"REXO1, REX1, ELOABP1, TCEB3BP1"	"RNA exonuclease 1, S. cerevisiae, homolog of"	REXO1	57455	ENSG00000079313			Rexo1 (MGI:1914182)			
chr19	1816158	1816237	19p13.3	19p13.3		615201	MIR1909	Micro RNA 1909	MIR1909	100302210							
chr19	1852398	1863564	19p13.3	19p13.3		606139	"KLF16, BTEB4, DRRF"	Kruppel-like factor 16	KLF16	83855	ENSG00000129911						
chr19	1905213	1913446	19p13.3	19p13.3		615302	"ADAT3, TAD3, MRT36"	"Adenosine deaminase, tRNA-specific, 3"	ADAT3	113179	ENSG00000213638		"Mental retardation, autosomal recessive 36, 615286 (3), Autosomal recessive"	Adat3 (MGI:1924344)			
chr19	1905213	1926016	19p13.3	19p13.3		613764	SCAMP4	Secretory carrier membrane protein 4	SCAMP4	113178	ENSG00000227500			Scamp4 (MGI:1928947)			
chr19	1941148	1981337	19p13.3	19p13.3		602214	CSNK1G2	"Casein kinase 1, gamma-2"	CSNK1G2	1455	ENSG00000133275			Csnk1g2 (MGI:1920014)			
chr19	2037470	2051277	19p13.3	19p13.3		605069	"MKNK2, MNK2, GPRK7"	Mitogen-activated protein kinase-interacting serine/threonine kinase-2	MKNK2	2872	ENSG00000099875			Mknk2 (MGI:894279)			
chr19	2100987	2151625	19p13.3	19p13.3		607246	"AP3D1, HPS10"	"Adaptor-related protein complex 3, delta-1 subunit"	AP3D1	8943	ENSG00000065000	mutation identified in 1 HPS10 patient	"?Hermansky-Pudlak syndrome 10, 617050 (3), Autosomal recessive"	Ap3d1 (MGI:107734)			
chr19	2163962	2232577	19p13.3	19p13.3		607375	"DOT1L, DOT1, KIAA1814"	"Dot1, yeast, homolog of"	DOT1L	84444	ENSG00000104885			Dot1l (MGI:2143886)			
chr19	2229951	2236723	19p13.3	19p13.3		617834	"PLEKHJ1, GNRPX"	"Pleckstrin homology domain-containing protein, family J, member 1"	PLEKHJ1	55111	ENSG00000104886			Plekhj1 (MGI:1925920)			
chr19	2236816	2248678	19p13.3-p13.2	19p13.3		600796	"SF3A2, SAP62, PRP11"	"Splicing factor 3a, subunit 2, 66kD"	SF3A2	8175	ENSG00000104897						
chr19	2249278	2252072	19p13.3-p13.2	19p13.3		600957	"AMH, MIF"	Anti-Mullerian hormone	AMH	268	ENSG00000104899		"Persistent Mullerian duct syndrome, type I, 261550 (3), Autosomal recessive"	Amh (MGI:88006)			
chr19	2252250	2260812	19p13.3	19p13.3		608743	"JSRP1, JP45"	Junctional sarcoplasmic reticulum protein 1	JSRP1	126306	ENSG00000167476			Jsrp1 (MGI:1916700)			
chr19	2269485	2273487	19p13.3	19p13.3		601579	OAZ1	Ornithine decarboxylase antizyme 1	OAZ1	4946	ENSG00000104904			Oaz1 (MGI:109433)			
chr19	2289774	2308156	19p13.3	19p13.3		609792	"LRRN6B, LINGO3, LERN2"	"Leucine-rich repeat protein, neuronal, 6B"	LINGO3	645191	ENSG00000220008			Lingo3 (MGI:3609246)			
chr19	2321520	2328629	19p13.3	19p13.3		607287	LSM7	LSM7 protein	LSM7	51690	ENSG00000130332			Lsm7 (MGI:1913344)			
chr19	2328570	2355101	19p13.3	19p13.3		608239	"SNPPL2B, IMP4, KIAA1532"	Signal peptide peptidase-like 2B	SPPL2B	56928	ENSG00000005206			Sppl2b (MGI:1920468)			
chr19	2385253	2426260	19p13.3	19p13.3		610477	TMPRSS9	"Transmembrane protease, serine 9"	TMPRSS9	360200	ENSG00000178297			Tmprss9 (MGI:3612246)			
chr19	2425623	2427915	19p13.3	19p13.3		607383	TIMM13	"Translocase of inner mitochondrial membrane 13, yeast, homolog of"	TIMM13	26517	ENSG00000099800			Timm13 (MGI:1353432)			
chr19	2428164	2456967	19p13.3	19p13.3		150341	"LMNB2, LMN2, EPM9"	Lamin B2	LMNB2	84823	ENSG00000176619	mutation identified in 1 EPM9 family	"?Epilepsy, progressive myoclonic, 9, 616540 (3), Autosomal recessive; {Lipodystrophy, partial, acquired, susceptibility to}, 608709 (3), Autosomal dominant"	Lmnb2 (MGI:96796)			
chr19	2476124	2478258	19p13.3	19p13.3		604948	"GADD45B, MYD118"	"Growth arrest- and DNA damage-inducible gene 45, beta"	GADD45B	4616	ENSG00000099860			Gadd45b (MGI:107776)			
chr19	2714566	2721391	19p13.3	19p13.3		607862	"DIRAS1, RIG"	"DIRAS family, GTP-binding Ras-like protein 1"	DIRAS1	148252	ENSG00000176490			Diras1 (MGI:2183442)			
chr19	2732523	2740075	19p13.3	19p13.3		612168	"SLC39A3, ZIP3"	"Solute carrier family 39, zinc transporter, member 3"	SLC39A3	29985	ENSG00000141873			Slc39a3 (MGI:2147269)			
chr19	2754713	2783355	19p13	19p13.3		603419	"SGTA, SGT"	"Small glutamine-rich tetratricopeptide repeat-containing protein, alpha"	SGTA	6449	ENSG00000104969			Sgta (MGI:1098703)			
chr19	2785459	2813603	19p13.3	19p13.3		601117	THOP1	Thimet oligopeptidase-1	THOP1	7064	ENSG00000172009			Thop1 (MGI:1354165)			
chr19	2933217	2944970	19p	19p13.3		194551	ZNF77	Zinc finger protein-77 (pT1)	ZNF77	58492	ENSG00000175691						
chr19	2977409	2995183	19p13.3	19p13.3		612399	"TLE6, GRG6, PREMBL"	Transducin-like enhancer of split 6	TLE6	79816	ENSG00000104953		"Preimplantation embryonic lethality, 616814 (3), Autosomal recessive"	Tle6 (MGI:2149593)			
chr19	2997637	3047634	19p13.3	19p13.3		601041	"TLE2, ESG2"	Transducin-like enhancer of split 2 (homolog of Drosophila E(spl))	TLE2	7089	ENSG00000065717			Tle2 (MGI:104635)			
chr19	3052909	3063106	19p13.3	19p13.3		600188	AES	Amino-terminal enhancer of split	AES	166	ENSG00000104964			Aes (MGI:95806)			
chr19	3094409	3124001	19p13	19p13.3		139313	"GNA11, HHC2, HYPOC2"	"Guanine nucleotide-binding protein, Gq class, GNA11"	GNA11	2767	ENSG00000088256		"Hypocalcemia, autosomal dominant 2, 615361 (3), Autosomal dominant; Hypocalciuric hypercalcemia, type II, 145981 (3), Autosomal dominant"	Gna11 (MGI:95766)			
chr19	3136031	3163768	19p13	19p13.3		139314	"GNA15, GNA16"	Guanine nucleotide-binding protein (G protein) alpha 15 (Gq class)	GNA15	2769	ENSG00000060558			Gna15 (MGI:95770)			
chr19	3178737	3180331	19p13.3	19p13.3		603751	"S1PR4, EDG6, S1P4"	Sphingosine-1-phosphate receptor 4	S1PR4	8698	ENSG00000125910			S1pr4 (MGI:1333809)			
chr19	3224675	3297075	19p13	19p13.3		612680	"CELF5, BRUNOL5"	"CUGbp- and ELAV-like family, member 5"	CELF5	60680	ENSG00000161082			Celf5 (MGI:2442333)			
chr19	3359562	3469216	19p13.3	19p13.3		600729	NFIC	Nuclear factor I/C (CCAAT-binding transcription factor)	NFIC	4782	ENSG00000141905	order: cen-NFIX-NFIC-tel		Nfic (MGI:109591)			
chr19	3490820	3500939	19p13.3	19p13.3		611262	"DOHH, HLRC1"	Deoxyhypusine hydroxylase	DOHH	83475	ENSG00000129932			Dohh (MGI:1915964)			
chr19	3506262	3536756	19p13.3	19p13.3		603619	"HCDH, FZR"	"CDH1/HCT1, S. cerevisiae, homolog of"	FZR1	51343	ENSG00000105325			Fzr1 (MGI:1926790)			
chr19	3538269	3557591	19p13.3	19p13.3		617745	"MFSD12, PP3501"	Major facilitator superfamily domain-containing protein 12	MFSD12	126321	ENSG00000161091			Mfsd12 (MGI:3604804)			
chr19	3572915	3579082	19p13.3	19p13.3		605535	"HMG20B, BRAF35"	High mobility group protein 20B	HMG20B	10362	ENSG00000064961			Hmg20b (MGI:1341190)			
chr19	3585530	3593540	19p13.3	19p13.3		608792	"GIPC3, DFNB15, DFNB72, DFNB95"	GAIP C-terminus-interacting protein 3	GIPC3	126326	ENSG00000179855		"Deafness, autosomal recessive 15, 601869 (3), Autosomal recessive"	Gipc3 (MGI:2387006)			
chr19	3594505	3608748	19p13.3	19p13.3		188070	"TBXA2R, BDPLT13"	Thromboxane A2 receptor	TBXA2R	6915	ENSG00000006638		"{Bleeding disorder, platelet-type, 13, susceptibility to}, 614009 (3), Autosomal dominant"	Tbxa2r (MGI:98496)			
chr19	3630180	3700491	19p13.3	19p13.3		606102	"PIP5K1C, LCCS3"	"Phosphatidylinositol-4-phosphate 5-kinase, type I, gamma"	PIP5K1C	23396	ENSG00000186111		"Lethal congenital contractural syndrome 3, 611369 (3), Autosomal recessive"	Pip5k1c (MGI:1298224)			
chr19	3708336	3750812	19p13.3	19p13.3		612689	"TJP3, ZO3"	Tight junction protein 3	TJP3	27134	ENSG00000105289			Tjp3 (MGI:1351650)			
chr19	3750772	3761695	19p13.3	19p13.3		604262	"APBA3, X11L2, MINT3"	"Amyloid beta A4 precursor protein-binding, family A, member 3"	APBA3	9546	ENSG00000011132			Apba3 (MGI:1888527)			
chr19	3762666	3767564	19p13.3	19p13.3		611858	MRPL54	Mitochondrial ribosomal protein L54	MRPL54	116541	ENSG00000183617			Mrpl54 (MGI:1913297)			
chr19	3769088	3772220	19p13.3	19p13.3		610362	"RAX2, RAXL1, QRX, CORD11, ARMD6"	Retina and anterior neural fold homeobox 2	RAX2	84839	ENSG00000173976	mutation identified in 1 ARMD6 patient	"Cone-rod dystrophy 11, 610381 (3), Autosomal dominant; ?Macular degeneration, age-related, 6, 613757 (3)"				
chr19	3777968	3801811	19p13.3	19p13.3		600038	"MATK, HYL, CTK"	Megakaryocyte-associated tyrosine kinase	MATK	4145	ENSG00000007264			Matk (MGI:99259)			
chr19	3880619	3928081	19p13.3	19p13.3		608179	"ATCAY, CLAC, KIAA1872"	Caytaxin	ATCAY	85300	ENSG00000167654		"Ataxia, cerebellar, Cayman type, 601238 (3), Autosomal recessive"	Atcay (MGI:2448730)			
chr19	3958452	3971122	19q13.3	19p13.3		603289	ZIPK	ZIP kinase	DAPK3	1613	ENSG00000167657			Dapk3 (MGI:1203520)			
chr19	3976055	3985462	19pter-q12	19p13.3		130610	"EEF2, EF2, SCA26"	Eukaryotic translation elongation factor-2	EEF2	1938	ENSG00000167658	mutation identified in 1 family	"?Spinocerebellar ataxia 26, 609306 (3), Autosomal dominant"	Eef2 (MGI:95288)			
chr19	4007597	4039385	19p13.3	19p13.3		605989	"PIAS4, PIASY"	Protein inhibitor of activated STAT4	PIAS4	51588	ENSG00000105229			Pias4 (MGI:2136940)			
chr19	4043303	4066944	19p13.3	19p13.3		605878	"ZBTB7A, FBI1, LRF"	Zinc finger and BTB domain containing 7A	ZBTB7A	51341	ENSG00000178951			Zbtb7a (MGI:1335091)			
chr19	4090320	4124183	19p13.3	19p13.3		601263	"MAP2K2, PRKMK2, MEK2, MKK2, CFC4"	Mitogen-activated protein kinase kinase 2	MAP2K2	5605	ENSG00000126934	previously assigned to 7q32	"Cardiofaciocutaneous syndrome 4, 615280 (3)"	Map2k2 (MGI:1346867)			
chr19	4153600	4173053	19p13.3	19p13.3		611998	"CREB3L3, CREBH"	cAMP responsive element-binding protein 3-like 3	CREB3L3	84699	ENSG00000060566			Creb3l3 (MGI:2384786)			
chr19	4174108	4182603	19p13.3	19p13.3		606211	"SIRT6, SIR2L6"	"Sirtuin 6 (Sir2, S. cerevisiae, homolog of, 6)"	SIRT6	51548	ENSG00000077463			Sirt6 (MGI:1354161)			
chr19	4229195	4237538	19p13.3	19p13.3		605816	EBI3	Epstein-Barr virus-induced gene 3	EBI3	10148	ENSG00000105246			Ebi3 (MGI:1354171)			
chr19	4278600	4290722	19p13.3	19p13.3		610481	SHD	SH2 domain-containing protein D	SHD	56961	ENSG00000105251			Shd (MGI:1099461)			
chr19	4292226	4302438	19p13.3	19p13.3		614715	"TMIGD2, IGPR1"	Transmembrane and immunoglobulin domains-containing protein 2 `	TMIGD2	126259	ENSG00000167664						
chr19	4304593	4323845	19p13.3	19p13.3		609828	"FSD1, GLFND"	Fibronectin type 3 and SPRY domains-containing protein 1	FSD1	79187	ENSG00000105255			Fsd1 (MGI:1934858)			
chr19	4324042	4338876	19p13.3	19p13.3		607881	"STAP2, BKS"	Signal-transducing adaptor protein 2	STAP2	55620	ENSG00000178078			Stap2 (MGI:2147039)			
chr19	4360366	4400567	19p13.3	19p13.3		601768	"SH3GL1, EEN"	SH3 domain GRB2-like 1 (Extra 11-19 leukemia fusion gene)	SH3GL1	6455	ENSG00000141985		"Leukemia, acute myeloid, 601626 (1), Autosomal dominant"	Sh3gl1 (MGI:700010)			
chr19	4402595	4448321	19p13.3	19p13.3		601246	"CHAF1A, CAF1B, CAF1P150"	"Chromatin assembly factor I, subunit A"	CHAF1A	10036	ENSG00000167670			Chaf1a (MGI:1351331)			
chr19	4445005	4458758	19p13	19p13.3		611946	"UBXN6, UBXD1"	UBX domain protein 6	UBXN6	80700	ENSG00000167671			Ubxn6 (MGI:1913780)			
chr19	4472195	4502219	19p13.3	19p13.3		617884	"HDGFL2, HDGFRP2"	Hepatoma-derived growth factor-like protein 2	HDGFL2	84717	ENSG00000167674			Hdgfl2 (MGI:1194492)			
chr19	4502179	4520284	19p13.3	19p13.3		613247	"PLIN4, KIAA1881"	Perilipin 4	PLIN4	729359	ENSG00000167676			Plin4 (MGI:1929709)			
chr19	4522530	4535195	19p13.3	19p13.3		613248	"PLIN5, LSDP5"	Perilipin 5	PLIN5	440503	ENSG00000214456			Plin5 (MGI:1914218)			
chr19	4537214	4540023	19p13.3	19p13.3		611289	"LRG1, LRG"	Leucine-rich alpha-2-glycoprotein 1	LRG1	116844	ENSG00000171236			Lrg1 (MGI:1924155)			
chr19	4542587	4581483	19p13.3	19p13.3		608873	SEMA6B	Semaphorin 6B	SEMA6B	10501	ENSG00000167680			Sema6b (MGI:1202889)			
chr19	4657544	4670402	19p13.3	19p13.3		606746	"C19orf10, SF20, IL25"	Stroma-derived growth factor 20	MYDGF	56005	ENSG00000074842			Mydgf (MGI:2156020)			
chr19	4724069	4724140	19p13.3	19p13.3		615303	TRNAG3	Transfer RNA glycine 3	TRG-TCC1-1	7197							
chr19	4724634	4724706	19p13.3	19p13.3		615304	TRNAV32	Transfer RNA valine 32	TRV-CAC3-1	100189416							
chr19	4791715	4795558	19p13.3	19p13.3		613538	FEM1A	"Fem1, C. elegans, homolog of, A"	FEM1A	55527	ENSG00000141965			Fem1a (MGI:1335089)			
chr19	4815923	4831741	19p13.3	19p13.3		607601	"TICAM1, TRIF, IIAE6"	TIR domain-containing adaptor molecule 1	TICAM1	148022	ENSG00000127666		"{Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6}, 614850 (3), Autosomal recessive, Autosomal dominant"	Ticam1 (MGI:2147032)			
chr19	4838333	4867767	19p13.3	19p13.3		602702	"PLIN3, M6PRBP1, TIP47"	Perilipin 3	PLIN3	10226	ENSG00000105355			Plin3 (MGI:1914155)			
chr19	4903079	4962153	19p13.3	19p13.3		607990	"UHRF1, ICBP90, NP95"	Ubiquitin-like protein containing PHD and RING finger domains 1	UHRF1	29128	ENSG00000276043			Uhrf1 (MGI:1338889)			
chr19	4969086	5153602	19p13.3	19p13.3		609765	"KDM4B, JMJD2B, KIAA0876"	Lysine-specific demethylase 4B	KDM4B	23030	ENSG00000127663			Kdm4b (MGI:2442355)			
chr19	5205502	5340802	19p13.3	19p13.3		601576	PTPRS	"Protein tyrosine phosphatase, receptor type, sigma"	PTPRS	5802	ENSG00000105426			Ptprs (MGI:97815)			
chr19	5455414	5456855	19p13.3	19p13.3		612063	"ZNRF4, SPERIZIN"	Zinc finger and ring finger protein 4	ZNRF4	148066	ENSG00000105428			Znrf4 (MGI:1341258)			
chr19	5558166	5568033	19p13.3	19p13.3		615241	TINCR	Terminal differentiation-induced noncoding RNA	TINCR	257000							
chr19	5586992	5622926	19p13.3	19p13.3		608066	"SAFB2, KIAA0138"	Scaffold attachment factor B2	SAFB2	9667	ENSG00000130254			Safb2 (MGI:2146808)			
chr19	5623034	5668477	19p13.3-p13.2	19p13.3		602895	"SAFB, HET"	Scaffold attachment factor B	SAFB	6294	ENSG00000160633			Safb (MGI:2146974)			
chr19	5678413	5680895	19p13.3	19p13.3		616658	"C19orf70, MIC13, QIL1"	Chromosome 19 open reading frame 70	C19orf70	125988	ENSG00000174917			2410015M20Rik (MGI:2442174)			
chr19	5690260	5691666	19p13.3	19p13.3		617893	RPL36	Ribosomal protein L36	RPL36	25873	ENSG00000130255			Rpl36-ps12 (MGI:3782787)			
chr19	5691833	5720451	19p13.2	19p13.3		605490	"LONP1, PRSS15, LON, CODASS"	"lon peptidase 1, mitochondrial"	LONP1	9361	ENSG00000196365		"CODAS syndrome, 600373 (3), Autosomal recessive"	Lonp1 (MGI:1921392)			
chr19	5720155	5778733	19p13.3	19p13.3		617490	"CATSPERD, TMEM146"	"Cation channel, sperm-associated, auxiliary subunit delta"	CATSPERD	257062	ENSG00000174898			Catsperd (MGI:2147030)			
chr19	5805386	5828323	19p13.3	19p13.3		602018	"NRTN, NTN"	Neurturin	NRTN	4902	ENSG00000171119			Nrtn (MGI:108417)			
chr19	5830625	5840018	19p13.3	19p13.3		136836	FUT6	"Fucosyltransferase 6 (alpha (1,3) fucosyltransferase)"	FUT6	2528	ENSG00000156413	"in cluster with FUT3, FUT5"	"Fucosyltransferase 6 deficiency, 613852 (3)"				
chr19	5842887	5851473	19p13.3	19p13.3		111100	"FUT3, LE"	Fucosyltransferase 3	FUT3	2525	ENSG00000171124	cen-FUT5-23kb-FUT3-14kb-FUT6-ter	"[Blood group, Lewis] (3)"				
chr19	5865825	5870539	19p13.3	19p13.3		136835	FUT5	"Fucosyltransferase 5 (alpha (1,3) fucosyltransferase)"	FUT5	2527	ENSG00000130383	cen-FUT5-FUT3-FUT6-ter					
chr19	5891275	5904012	19p13.3	19p13.3		612638	NDUFA11	"NADH-dehydrogenase 1 alpha subcomplex, 11"	NDUFA11	126328	ENSG00000174886		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	"Ndufa11,Gm4943 (MGI:3645174,MGI:1917125)"			
chr19	5904840	5910251	19p13.3	19p13.3		617204	VMAC	Vimentin-type intermediate filament-associated coiled-coil protein	VMAC	400673	ENSG00000187650			Vmac (MGI:2146912)			
chr19	5913643	5916210	19p13.3	19p13.3		114212	CAPS	Calcyphosine	CAPS	828	ENSG00000105519						
chr19	5916138	5978308	19p13.3	19p13.3		603327	RANBP3	RAN-binding protein-3	RANBP3	8498	ENSG00000031823			Ranbp3 (MGI:1919060)			
chr19	5993163	6110652	19p13.3-p13.2	19p13.3		142765	RFX2	Regulatory factor (trans-acting) 2 (influences HLA class II expression)	RFX2	5990	ENSG00000087903			Rfx2 (MGI:106583)			
chr19	6135632	6193102	19p13.3	19p13.3		614363	"ACSBG2, BGR"	"Acyl-CoA synthetase, bubblegum family, member 2"	ACSBG2	81616	ENSG00000130377			Acsbg2 (MGI:3587728)			
chr19	6210380	6279947	19p13.3	19p13.3		159556	"MLLT1, ENL"	"Myeloid/lymphoid or mixed-lineage leukemia, translocated to, 1"	MLLT1	4298	ENSG00000130382	fuses with ALL1		Mllt1 (MGI:1927238)			
chr19	6306141	6360367	19p13.3	19p13.3		613491	ACER1	Alkaline ceraminidase 1	ACER1	125981	ENSG00000167769			Acer1 (MGI:2181962)			
chr19	6361451	6368903	19p13.3	19p13.3		601119	"CLPP, PRLTS3, DFNB81"	"ATP-dependent protease ClpAP, E. coli, proteolytic subunit, homolog of"	CLPP	8192	ENSG00000125656		"Perrault syndrome 3, 614129 (3), Autosomal recessive"	Clpp (MGI:1858213)			
chr19	6372432	6375249	19p13.3	19p13.3		613305	"ALKBH7, ABH7"	"AlkB, E. coli, homolog of, 7"	ALKBH7	84266	ENSG00000125652			Alkbh7 (MGI:1913650)			
chr19	6375147	6375915	19p13.3	19p13.3		602921	PSPN	Persephin	PSPN	5623	ENSG00000125650			Pspn (MGI:1201684)			
chr19	6379568	6393279	19p13.3	19p13.3		189968	"GTF2F1, RAP74"	"General transcription factor IIF, polypeptide 1 (74kD subunit)"	GTF2F1	2962	ENSG00000125651			Gtf2f1 (MGI:1923848)			
chr19	6413103	6424810	19p13.3	19p13.3		603445	"KHSRP, KSRP, FUBP2, FBP2"	KH-type splicing regulatory protein	KHSRP	8570	ENSG00000088247			Khsrp (MGI:1336214)			
chr19	6426036	6436266	19p13.3	19p13.3		610822	SLC25A41	"Solute carrier family 25, member 41"	SLC25A41	284427	ENSG00000181240			Slc25a41 (MGI:2144215)			
chr19	6463776	6467220	19p13.3	19p13.3		609737	CRB3	"Crumbs, Drosophila, homolog of, 3"	CRB3	92359	ENSG00000130545						
chr19	6467203	6481807	19p13.3	19p13.3		613634	DENND1C	DENN/MADD domain-containing protein 1C	DENND1C	79958	ENSG00000205744			Dennd1c (MGI:1918035)			
chr19	6494318	6502847	19p13.3	19p13.3		602662	"TUBB4A, DYT4, HLD6"	"Tubulin, beta-4A"	TUBB4A	10382	ENSG00000104833		"Dystonia 4, torsion, autosomal dominant, 128101 (3), Autosomal dominant; Leukodystrophy, hypomyelinating, 6, 612438 (3), Autosomal dominant"	Tubb4a (MGI:107848)			
chr19	6530998	6535927	19p13.3	19p13.3		606182	TNFSF9	"Tumor necrosis factor ligand superfamily, member 9"	TNFSF9	8744	ENSG00000125657						
chr19	6581645	6591151	19p13	19p13.3		602840	"TNFSF7, CD70, CD27L"	"Tumor necrosis factor ligand superfamily, member 7 (CD70 antigen)"	CD70	970	ENSG00000125726			Cd70 (MGI:1195273)			
chr19	6658125	6670594	19p13.3	19p13.3		604520	"TNFSF14, HVEML"	"Tumor necrosis factor ligand superfamily, member 14"	TNFSF14	8740	ENSG00000125735			Tnfsf14 (MGI:1355317)			
chr19	6677834	6720681	19p13.3-p13.2	19p13.3		120700	"C3, ARMD9, AHUS5"	Complement component-3	C3	718	ENSG00000125730	LE ~7cM in males vs. C3 RFLP	"C3 deficiency, 613779 (3), Autosomal recessive; {Hemolytic uremic syndrome, atypical, susceptibility to, 5}, 612925 (3), Autosomal dominant; {Macular degeneration, age-related, 9}, 611378 (3)"	C3 (MGI:88227)			
chr19	6739681	6751525	19p13.3	19p13.3		604504	"TRIP10, CIP4"	Thyroid hormone receptor interactor 10	TRIP10	9322	ENSG00000125733			Trip10 (MGI:2146901)			
chr19	6772667	6857365	19p13.3-p13.2	19p13.3		164875	"VAV1, VAV"	Oncogene VAV1	VAV1	7409	ENSG00000141968	close to INSR		Vav1 (MGI:98923)			
chr19	6887548	6940452	19p13.3	19p13.3-p13.2		600493	"ADGRE1, EMR1"	Adhesion G protein-coupled receptor E1	ADGRE1	2015	ENSG00000174837			Adgre1 (MGI:106912)			
chr19	6900000	50900000	19p13.2-q13.3			164953	"LPSA, D19S381E"	"Oncogene liposarcoma (DNA segment, single copy, expressed, probes MC15, MC6)"		8177			Liposarcoma (1)				
chr19	6900000	12600000	19p13.2			614223	NRCLP6	Narcolepsy 6		100689216		associated with rs2305795	"Narcolepsy 6, 614223 (2)"				
chr19	6900000	19900000	19p13.2-p13.1			607324	PAPA3	"Polydactyly, postaxial, type A3"		338333		between D19S1165 and D19S929	"Polydactyly, postaxial, type A3, 607324 (2)"				
chr19	6900000	12600000	19p13.2			184700	"PCOS1, PCO1, PCO"	Polycystic ovary syndrome 1	PCOS1	5120		max lod at D19S884	"Polycystic ovary syndrome 1, 184700 (2), Autosomal dominant"				
chr19	6900000	12600000	19p13.2			603386	TCO	"Thyroid carcinoma, nonmedullary, with cell oxyphilia"		50975			"Thyroid carcinoma, nonmedullary, with cell oxyphilia, 603386 (2)"				
chr19	6952499	6990845	19p13.3	19p13.2		612305	"ADGRE4P, EMR4, GPR127, EMR4P, FIRE"	"Adhesion G protein-coupled receptor E4, pseudogene"	ADGRE4P	326342							
chr19	7049339	7051734	19p13.2	19p13.2		607964	MBD3L2	Methyl-CpG binding domain protein 3-like 2	MBD3L2	125997	ENSG00000230522			Mbd3l2 (MGI:2158460)			
chr19	7112254	7294404	19p13.2	19p13.2		147670	"INSR, HHF5"	Insulin receptor	INSR	3643	ENSG00000171105	1 gene for alpha and beta subunits	"Diabetes mellitus, insulin-resistant, with acanthosis nigricans, 610549 (3); Hyperinsulinemic hypoglycemia, familial, 5, 609968 (3), Autosomal dominant; Leprechaunism, 246200 (3), Autosomal recessive; Rabson-Mendenhall syndrome, 262190 (3), Autosomal recessive"	Insr (MGI:96575)			
chr19	7348900	7476989	19p13.2	19p13.2		616432	"ARHGEF18, KIAA0521, RP78"	Rho guanine nucleotide exchange factor 18	ARHGEF18	23370	ENSG00000268861		"Retinitis pigmentosa 78, 617433 (3), Autosomal recessive"	Arhgef18 (MGI:2142567)			
chr19	7476869	7494976	19p13.3	19p13.2		607583	PEX11G	Peroxisome biogenesis factor 11G	PEX11G	92960	ENSG00000104883			Pex11g (MGI:1920905)			
chr19	7522609	7534008	19p13.3-p13.2	19p13.2		605248	"MCOLN1, ML4"	Mucolipin 1	MCOLN1	57192	ENSG00000090674		"Mucolipidosis IV, 252650 (3), Autosomal recessive"	Mcoln1 (MGI:1890498)			
chr19	7534151	7561766	19p13.3	19p13.2		603197	"PNPLA6, NTE, SPG39, NTEMND, BNHS, LNMS, OMCS"	Patatin-like phospholipase domain-containing protein 6	PNPLA6	10908	ENSG00000032444	mutation identified in 1 LMNS family	"Boucher-Neuhauser syndrome, 215470 (3), Autosomal recessive; ?Laurence-Moon syndrome, 245800 (3), Autosomal recessive; Oliver-McFarlane syndrome, 275400 (3), Autosomal recessive; Spastic paraplegia 39, autosomal recessive, 612020 (3), Autosomal recessive"	Pnpla6 (MGI:1354723)			
chr19	7595901	7618309	19p13.2	19p13.2		612685	"CAMSAP3, NEZHA, KIAA1543"	Calmodulin-regulated spectrin-associated protein 3	CAMSAP3	57662	ENSG00000076826			Camsap3 (MGI:1916947)			
chr19	7619524	7629552	19p13.2	19p13.2		610850	XAB2	XPA-binding protein 2	XAB2	56949	ENSG00000076924			Xab2 (MGI:1914689)			
chr19	7629784	7631623	19p13.2	19p13.2		614770	"PET100, C19orf79"	"PET100, S. cerevisiae, homolog of"	PET100	100131801	ENSG00000229833		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Pet100 (MGI:3615306)			
chr19	7637100	7647873	19p13.3-p13.2	19p13.2		601717	"STXBP2, UNC18B, FHL5"	Syntaxin binding protein 2	STXBP2	6813	ENSG00000076944		"Hemophagocytic lymphohistiocytosis, familial, 5, 613101 (3)"	Stxbp2 (MGI:107370)			
chr19	7669085	7670453	19p13.2	19p13.2		605565	"RETN, RSTN, FIZZ3"	Resistin	RETN	56729	ENSG00000104918		"{Diabetes mellitus, noninsulin-dependent, susceptibility to}, 125853 (3), Autosomal dominant; {Hypertension, insulin resistance-related, susceptibility to}, 125853 (3), Autosomal dominant"	Retn (MGI:1888506)			
chr19	7677056	7679832	19p13.3	19p13.2		609565	MCEMP1	Mast cell-expressed membrane protein 1	MCEMP1	199675	ENSG00000183019			Mcemp1 (MGI:1916439)			
chr19	7688756	7702754	19p13.3	19p13.2		151445	"FCER2, FCE2, CD23, CLEC4J"	"Fc fragment of IgE, low affinity II, receptor for (CD23A)"	FCER2	2208	ENSG00000104921			Fcer2a (MGI:95497)			
chr19	7728956	7732180	19p13.3	19p13.2		616256	"CLEC4G, LSECTIN"	"C-type lectin domain family 4, member G"	CLEC4G	339390	ENSG00000182566			Clec4g (MGI:1923113)			
chr19	7739992	7747608	19p13.3	19p13.2		604672	"CD209, CDSIGN"	CD209 antigen	CD209	30835	ENSG00000090659		"{Dengue fever, protection against}, 614371 (3); {HIV type 1, susceptibility to}, 609423 (3); {Mycobacterium tuberculosis, susceptibility to}, 607948 (3)"	Cd209e (MGI:2157948)			
chr19	7763051	7770558	19p13.3	19p13.2		605872	"CLEC4M, CD209L, LSIGN, DCSIGNR"	"C-type lectin domain family 4, member M"	CLEC4M	10332	ENSG00000104938		"SARS infection, protection against, 605872 (2)"	Cd209a (MGI:2157942)			
chr19	7888504	7902022	19p13.2	19p13.2		612891	LRRC8E	Leucine-rich repeat-containing protein 8E	LRRC8E	80131	ENSG00000171017			Lrrc8e (MGI:1919517)			
chr19	7903779	7914482	19p13.2	19p13.2		603014	"MAP2K7, PRKMK7, MKK7, JNKK2, MAPKK7"	Mitogen-activated protein kinase kinase 7	MAP2K7	5609	ENSG00000076984			Map2k7 (MGI:1346871)			
chr19	7920308	7923250	19p13.2	19p13.2		605076	"SNAPC2, SNAP45"	"Small nuclear RNA-activating protein complex, polypeptide 2"	SNAPC2	6618	ENSG00000104976			Snapc2 (MGI:1914861)			
chr19	7924495	7926165	19p13.2	19p13.2		600135	"CTXN1, CTXN"	Cortexin 1	CTXN1	404217	ENSG00000178531			Ctxn1 (MGI:88566)			
chr19	7926717	7943822	19p13.3-p13.2	19p13.2		605058	TIMM44	"Translocase of inner mitochondrial membrane 44, yeast, homolog of"	TIMM44	10469	ENSG00000104980			Timm44 (MGI:1343262)			
chr19	7958572	8005644	19p13.2	19p13.2		603466	"ELAVL1, HUR"	"Embryonic lethal, abnormal vision, Drosophila, homolog-like 1"	ELAVL1	1994	ENSG00000066044			Elavl1 (MGI:1100851)			
chr19	8052317	8062662	19p13.2	19p13.2		602565	"CCL25, SCYA25, TECK"	"Chemokine, C-C motif, ligand 25"	CCL25	6370	ENSG00000131142			Ccl25 (MGI:1099448)			
chr19	8209328	8262432	19p13.2	19p13.2		615334	"CERS4, LASS4, TRH1"	Ceramide synthase 4	CERS4	79603	ENSG00000090661			Cers4 (MGI:1914510)			
chr19	8302126	8308355	19p13.2	19p13.2		606475	"CD320, 8D6, 8D6A, TCBLR"	CD320 molecule	CD320	51293	ENSG00000167775		"Methylmalonic aciduria, transient, due to transcobalamin receptor defect, 613646 (3)"	Cd320 (MGI:1860083)			
chr19	8308602	8321412	19p13.2	19p13.2		602139	NDUFA7	"NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 7 (14.5kD, B14.5a)"	NDUFA7	4701	ENSG00000267855	previously assigned to 20p13		Ndufa7 (MGI:1913666)			
chr19	8321499	8322395	19p13.2	19p13.2		603685	"RPS28, DBA15"	Ribosomal protein S28	RPS28	6234	ENSG00000233927		"Diamond Blackfan anemia 15 with mandibulofacial dysostosis, 606164 (3), Autosomal dominant"	Rps28 (MGI:1859516)			
chr19	8322583	8343261	19p13.2	19p13.2		614611	KANK3	KN motif- and ankyrin repeat domain-containing protein 3	KANK3	256949	ENSG00000186994			Kank3 (MGI:1098615)			
chr19	8364126	8374374	19p13.3	19p13.2		605910	"ANGPTL4, PGAR, HFARP, FIAF, TGQTL"	Angiopoietin-like 4	ANGPTL4	51129	ENSG00000167772		"Plasma triglyceride level QTL, low, 615881 (3), Autosomal dominant"	Angptl4 (MGI:1888999)			
chr19	8390320	8404433	19p13.2	19p13.2		604198	"RAB11B, NDAGSCW"	Ras-associated protein RAB11B	RAB11B	9230	ENSG00000185236		"Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter, 617807 (3)"	Rab11b (MGI:99425)			
chr19	8413271	8439020	19p13.2	19p13.2		613332	2-Mar	Membrane-associated RING-CH finger protein 2	2-Mar	51257	ENSG00000099785			March2 (MGI:1925915)			
chr19	8444574	8489117	19p13.3-p13.2	19p13.2		160994	"HNRPM, HNRPM4, NAGR1"	Heterogeneous nuclear ribonucleoprotein M	HNRNPM	4670	ENSG00000099783			Hnrnpm (MGI:1926465)			
chr19	8520789	8577446	19p13.3-p13.2	19p13.2		601480	MYO1F	Myosin IF	MYO1F	4542	ENSG00000142347			Myo1f (MGI:107711)			
chr19	8580239	8610734	19p13.3-p13.2	19p13.2		608990	"ADAMTS10, WMS1"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 10"	ADAMTS10	81794	ENSG00000142303		"Weill-Marchesani syndrome 1, recessive, 277600 (3), Autosomal recessive"	Adamts10 (MGI:2449112)			
chr19	8842592	8843339	19p13.2	19p13.2		607963	MBD3L1	Methyl-CpG binding domain protein 3-like 1	MBD3L1	85509	ENSG00000170948			Mbd3l1 (MGI:1920753)			
chr19	8848839	9010389	19p13.2	19p13.2		606154	"MUC16, CA125"	Mucin 16	MUC16	94025	ENSG00000181143						
chr19	9140379	9163418	19p13	19p13.2		613864	"ZNF317, KIAA1588"	Zinc finger protein 317	ZNF317	57693	ENSG00000130803			Zfp317 (MGI:107775)			
chr19	9213849	9214870	19p13.2	19p13.2		611538	"OR7D4, OR19B"	"Olfactory receptor, family 7, subfamily D, member 4"	OR7D4	125958	ENSG00000174667			Olfr39 (MGI:1313142)			
chr19	9291139	9309713	19p13.2	19p13.2		609571	"ZNF699, FLJ38144"	Zinc finger protein 699	ZNF699	374879	ENSG00000196110						
chr19	9363019	9382616	19p13	19p13.2		601276	ZNF177	Zinc finger protein 177	ZNF177	7730	ENSG00000188629						
chr19	9412425	9435577	19p13.2	19p13.2		604751	"ZNF266, HZF1"	Zinc finger protein-266	ZNF266	10781	ENSG00000174652			Zfp266 (MGI:1924769)			
chr19	9565656	9584543	19p	19p13.2		194628	"ZNF121, D19S204"	Zinc finger protein-121 (clone ZHC32)	ZNF121	7675	ENSG00000197961						
chr19	9810266	9820527	19p13.2	19p13.2		609079	"FBXL12, FBL12"	F-box and leucine-rich repeat protein 12	FBXL12	54850	ENSG00000127452			Fbxl12 (MGI:1354738)			
chr19	9827879	9830120	19p13.2	19p13.2		606849	"UBL5, HUB1"	Ubiquitin-like 5	UBL5	59286	ENSG00000198258	pseudogene on 17p11.2		Ubl5 (MGI:1913427)			
chr19	9835206	9849688	19p13	19p13.2		601052	"PIN1, DOD"	"Peptidyl-prolyl cis/trans isomerase, NIMA-interacting"	PIN1	5300	ENSG00000127445			Pin1 (MGI:1346036)			
chr19	9853717	9936551	19p13.2	19p13.2		617492	"OLFM2, NOE2"	Olfactomedin 2	OLFM2	93145	ENSG00000105088			Olfm2 (MGI:3045350)			
chr19	9959560	10010531	19p13.2	19p13.2		120216	COL5A3	"Collagen, type V, alpha-3 polypeptide"	COL5A3	50509	ENSG00000080573			Col5a3 (MGI:1858212)			
chr19	10013248	10022277	19p13	19p13.2		608575	"RDH8, PRRDH"	Retinol dehydrogenase 8	RDH8	50700	ENSG00000080511			Rdh8 (MGI:2685028)			
chr19	10086118	10093251	19p13.2	19p13.2		616808	"C19orf66, RYDEN"	Chromosome 19 open reading frame 66	C19orf66	55337	ENSG00000130813			A230050P20Rik (MGI:2441788)			
chr19	10092336	10106406	19p13.2	19p13.2		609336	"ANGPTL6, AGF"	Angiopoietin-like 6	ANGPTL6	83854	ENSG00000130812			Angptl6 (MGI:1917976)			
chr19	10106222	10112002	19p13	19p13.2		607793	"PPAN, SSF1"	"Peter pan, Drosophila, homolog of"	PPAN	56342	ENSG00000130810	fuses with P2RY11		Ppan (MGI:2178445)			
chr19	10111520	10115388	19p13	19p13.2		602697	P2RY11	"Purinergic receptor P2Y, G protein-coupled, 11"	P2RY11	5032	ENSG00000244165	fuses with PPAN					
chr19	10115013	10119923	19p13.2	19p13.2		603913	"EIF3G, EIF3S4"	"Eukaryotic translation initiation factor 3, subunit G"	EIF3G	8666	ENSG00000130811			Eif3g (MGI:1858258)			
chr19	10133343	10195134	19p13.3-p13.2	19p13.2		126375	"DNMT1, MCMT, HSN1E, ADCADN"	DNA methyltransferase 1	DNMT1	1786	ENSG00000130816		"Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121 (3), Autosomal dominant; Neuropathy, hereditary sensory, type IE, 614116 (3), Autosomal dominant"	Dnmt1 (MGI:94912)			
chr19	10221432	10231271	19p13.2	19p13.2		605111	"S1PR2, EDG5, DFNB68"	Sphingosine-1-phosphate receptor 2	S1PR2	9294	ENSG00000267534		"Deafness, autosomal recessive 68, 610419 (3), Autosomal recessive"	S1pr2 (MGI:99569)			
chr19	10251961	10260059	19p13.2	19p13.2		611823	MRPL4	Mitochondrial ribosomal protein L4	MRPL4	51073	ENSG00000105364			Mrpl4 (MGI:2137210)			
chr19	10270840	10286614	19p13.3-p13.2	19p13.2		147840	ICAM1	Intercellular adhesion molecule-1	ICAM1	3383	ENSG00000090339	close to Ldlr in mouse	"{Malaria, cerebral, susceptibility to}, 611162 (3)"	Icam1 (MGI:96392)			
chr19	10286966	10288583	19p13.3	19p13.2		614088	"ICAM4, CD242, LW"	Intracellular adhesion molecule 4	ICAM4	3386	ENSG00000105371	"close to C3, LU"	"[Blood group, Landsteiner-Wiener], 111250 (3)"	Icam4 (MGI:1925619)			
chr19	10289350	10296777	19p13.2	19p13.2		601852	"ICAM5, TLCN, TLN"	Intercellular adhesion molecule 5 (telencephalin)	ICAM5	7087	ENSG00000105376			Icam5 (MGI:109430)			
chr19	10304802	10309556	19p13.2	19p13.2		611639	"ZGLP1, GLP1"	Zinc finger GATA-like protein 1	ZGLP1	100125288	ENSG00000220201			Zglp1 (MGI:3696042)			
chr19	10310210	10316014	19p13.2	19p13.2		614585	"FDX1L, FDX2"	Ferredoxin 1-like protein	FDX2	112812	ENSG00000267673			Fdx1l (MGI:1915415)			
chr19	10316211	10333637	19p13.2	19p13.2		609950	"RAVER1, KIAA1978"	"Raver1, mouse, homolog of"	RAVER1	125950	ENSG00000161847			Raver1 (MGI:1919016)			
chr19	10333775	10339833	19p13.3-p13.2	19p13.2		146631	"ICAM3, CDW50"	Intercellular adhesion molecule-3	ICAM3	3385	ENSG00000076662						
chr19	10350527	10380571	19p13.2	19p13.2		176941	"TYK2, IMD35"	Tyrosine kinase 2	TYK2	7297	ENSG00000105397		"Immunodeficiency 35, 611521 (3), Autosomal recessive"	Tyk2 (MGI:1929470)			
chr19	10391127	10403594	19p13.2	19p13.2		605065	CDC37	"Cell division cycle 37, S. cerevisiae, homolog of"	CDC37	11140	ENSG00000105401			Cdc37 (MGI:109531)			
chr19	10416772	10469630	19p13.2	19p13.2		600126	"PDE4A, DPDE2"	"Phosphodiesterase-4A, cAMP-specific (dunce, Drosophila, homolog phosphodiesterase E2)"	PDE4A	5141	ENSG00000065989			Pde4a (MGI:99558)			
chr19	10486119	10503377	19p13.2	19p13.2		606016	"KEAP1, KIAA0132"	Kelch-like ECH-associated protein 1	KEAP1	9817	ENSG00000079999			Keap1 (MGI:1858732)			
chr19	10512741	10517991	19p13.2	19p13.2		605146	"S1PR5, EDG8"	Sphingosine-1-phosphate receptor 5	S1PR5	53637	ENSG00000180739			S1pr5 (MGI:2150641)			
chr19	10543893	10553422	19p13.2	19p13.2		611340	"ATG4D, APG4D, AUTL4"	"Autophagy 4, S. cerevisiae, homolog of, D"	ATG4D	84971	ENSG00000130734			Atg4d (MGI:2444308)			
chr19	10566461	10568978	19p13	19p13.2		600927	CDKN2D	"Cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)"	CDKN2D	1032	ENSG00000129355	possible tumor suppressor		Cdkn2d (MGI:105387)			
chr19	10572670	10587314	19p13.2	19p13.2		607309	"AP1M2, MU1B"	"Adaptor-related protein complex 1, mu-2 subunit"	AP1M2	10053	ENSG00000129354			Ap1m2 (MGI:1336974)			
chr19	10602444	10644558	19p13.1	19p13.2		606106	"SLC44A2, CTL2"	"Solute carrier family 44, member 2"	SLC44A2	57153	ENSG00000129353			Slc44a2 (MGI:1915932)			
chr19	10654260	10692418	19p13	19p13.2		603182	"ILF3, NF90, DRBP76, MPHOSPH4, NFAR"	Interleukin enhancer-binding factor 3	ILF3	3609	ENSG00000129351			Ilf3 (MGI:1339973)			
chr19	10701435	10713366	19p13.2	19p13.2		609615	"QTRT1, TGT"	Queuine tRNA-ribosyltransferase 1	QTRT1	81890	ENSG00000213339			Qtrt1 (MGI:1931441)			
chr19	10718052	10831909	19p13.2	19p13.2		602378	"DNM2, CMTDIB, CMTDI1, CMT2M, LCCS5"	Dynamin-2	DNM2	1785	ENSG00000079805	1 LCCS5 family identified with mutation	"Centronuclear myopathy 1, 160150 (3), Autosomal dominant; Charcot-Marie-Tooth disease, axonal type 2M, 606482 (3), Autosomal dominant; Charcot-Marie-Tooth disease, dominant intermediate B, 606482 (3), Autosomal dominant; Lethal congenital contracture syndrome 5, 615368 (3), Autosomal recessive"	Dnm2 (MGI:109547)			
chr19	10817425	10817495	19p13.2	19p13.2		610719	"MIR199A1, MIRN199A1"	Micro RNA 199A1	MIR199A1	406976							
chr19	10832066	10836306	19p13.2	19p13.2		605395	"TMED1, IL1RL1LG"	Transmembrane p24 trafficking protein 1 (interleukin-1 receptor-like 1 ligand)	TMED1	11018	ENSG00000099203			Tmed1 (MGI:106201)			
chr19	10871576	10923077	19p13.2	19p13.2		603934	"CARM1, PRMT4"	Coactivator-associated arginine methyltransferase 1	CARM1	10498	ENSG00000142453			Carm1 (MGI:1913208)			
chr19	10922184	10929011	19p13.2	19p13.2		617522	YIPF2	"YIP1 domain family, member 2"	YIPF2	78992	ENSG00000130733			Yipf2 (MGI:1922016)			
chr19	10928735	10930253	19p13.2	19p13.2		617380	"TIMM29, C19orf52"	Translocase of inner mitochondrial membrane 29	TIMM29	90580	ENSG00000142444			Timm29 (MGI:1917023)			
chr19	10960921	11062281	19p13.2	19p13.2		603254	"SMARCA4, BRG1, RTPS2, MRD16, CSS4"	"SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4"	SMARCA4	6597	ENSG00000127616		"Coffin-Siris syndrome 4, 614609 (3), Autosomal dominant; {Rhabdoid tumor predisposition syndrome 2}, 613325 (3), Autosomal dominant"	Smarca4 (MGI:88192)			
chr19	11089361	11133829	19p13.2	19p13.2		606945	"LDLR, FHC, FH, LDLCQ2"	Low density lipoprotein receptor	LDLR	3949	ENSG00000130164	~20cM distal to C3	"Hypercholesterolemia, familial, 143890 (3), Autosomal dominant; LDL cholesterol level QTL2, 143890 (3), Autosomal dominant"	Ldlr (MGI:96765)			
chr19	11145493	11155996	19p13.2	19p13.2		609394	"SPC24, SPBC24"	"SPC24, NDC80 kinetochore complex component"	SPC24	147841	ENSG00000161888			Spc24 (MGI:1914879)			
chr19	11164266	11197566	19p13.2	19p13.2		614610	"KANK2, ANKRD25, KIAA1518, PPKWH, NPHS16"	KN motif- and ankyrin repeat domain-containing protein 2	KANK2	25959	ENSG00000197256		"Nephrotic syndrome 16, 617783 (3), Autosomal recessive; Palmoplantar keratoderma and woolly hair, 616099 (3), Autosomal recessive"	Kank2 (MGI:2384568)			
chr19	11199292	11262500	19p13.2	19p13.2		614194	"DOCK6, KIAA1395, AOS2"	Dedicator of cytokinesis 6	DOCK6	57572	ENSG00000130158		"Adams-Oliver syndrome 2, 614219 (3), Autosomal recessive"	Dock6 (MGI:1914789)			
chr19	11239618	11241942	19p13.2	19p13.2		616223	"ANGPTL8, C19orf80, LIPASIN"	Angiopoietin-like protein 8	ANGPTL8	55908	ENSG00000130173	within intron of DOCK6		Angptl8 (MGI:3643534)			
chr19	11296138	11326995	9q34	19p13.2		617580	"TSPAN16, TM4SF16"	Tetraspanin 16	TSPAN16	26526	ENSG00000130167						
chr19	11322045	11339667	19p13.2	19p13.2		604350	"RAD3D, GOV"	"Ras family, member RAB3D"	RAB3D	9545	ENSG00000105514			Rab3d (MGI:97844)			
chr19	11342511	11346458	19p13.2	19p13.2		613771	TMEM205	Transmembrane protein 205	TMEM205	374882	ENSG00000105518			Tmem205 (MGI:3045495)			
chr19	11374706	11376950	19p13.2	19p13.2		614536	"SWSAP1, ZSWIM7AP1, C19orf39"	SWIM-type zinc finger domain-containing protein 7-associated protein 1	SWSAP1	126074	ENSG00000173928			Swsap1 (MGI:1914212)			
chr19	11377204	11384341	19p13.3-p13.2	19p13.2		133171	EPOR	Erythropoietin receptor	EPOR	2057	ENSG00000187266		"[Erythrocytosis, familial, 1], 133100 (3), Autosomal dominant"	Epor (MGI:95408)			
chr19	11394055	11419341	19p13.2	19p13.2		616743	RGL3	Ral guanine nucleotide dissociation stimulator-like 3	RGL3	57139	ENSG00000205517			Rgl3 (MGI:1918996)			
chr19	11420604	11435781	19p13.2	19p13.2		615956	"CCDC151, CILD30"	Coiled-coil domain-containing protein 151	CCDC151	115948	ENSG00000198003		"Ciliary dyskinesia, primary, 30, 616037 (3), Autosomal recessive"	Ccdc151 (MGI:1924859)			
chr19	11435256	11450967	19p13.2-p13.1	19p13.2		177060	"PRKCSH, G19P1, PCLD1"	Protein kinase C substrate 80K-H	PRKCSH	5589	ENSG00000130175		"Polycystic liver disease 1, 174050 (3), Autosomal dominant"	Prkcsh (MGI:107877)			
chr19	11451325	11481045	19p13.2	19p13.2		603458	"ELAVL3, HUC, PLE21"	"Embryonic lethal, abnormal vision, Drosophila, homolog-like 3"	ELAVL3	1995	ENSG00000196361	centromeric to ELAVL1		Elavl3 (MGI:109157)			
chr19	11483426	11505922	19p13.2	19p13.2		611371	"ZNF653, ZIP67"	Zinc finger protein 653	ZNF653	115950	ENSG00000161914			Zfp653 (MGI:2442362)			
chr19	11505915	11529171	19p13.2	19p13.2		608388	"SITPEC, ECSIT"	"Signaling intermediate in toll pathway, evolutionarily conserved"	ECSIT	51295	ENSG00000130159			Ecsit (MGI:1349469)			
chr19	11538716	11550322	19p13.2	19p13.2		600806	"CNN1, SMCC"	Calponin 1	CNN1	1264	ENSG00000130176			Cnn1 (MGI:104979)			
chr19	11574659	11579007	19p13.3-p13.1	19p13.2		171640	"ACP5, SPENCDI"	"Acid phosphatase 5, tartrate resistant"	ACP5	54	ENSG00000102575	incorrectly assigned to 15 by A	"Spondyloenchondrodysplasia with immune dysregulation, 607944 (3), Autosomal recessive"				
chr19	11575254	11619158	19p13.2	19p13.2		612248	ZNF627	Zinc finger protein 627	ZNF627	199692	ENSG00000198551			Zfp867 (MGI:2681848)			
chr19	11887772	11980221	19p13.2	19p13.2		194543	ZNF69	Zinc finger protein-69 (Cos5)	ZNF69	7620	ENSG00000198429	previously assigned to 22q11.2					
chr19	12131349	12140406	19p13.3-p13.2	19p13.2		194557	"ZNF20, KOX13"	Zinc finger protein-14 (KOX 6)	ZNF20	7568	ENSG00000132010						
chr19	12163046	12189880	19p13.2-p13.12	19p13.2		604078	ZNF136	Zinc finger protein-136	ZNF136	7695	ENSG00000196646						
chr19	12224685	12294898	19p13.2	19p13.2		194542	"ZNF44, KOX7"	Zinc finger protein-44 (KOX7)	ZNF44	51710	ENSG00000197857	previously assigned to 16p11					
chr19	12429705	12441111	19p13.2	19p13.2		606697	ZK1	Zinc finger protein ZK1	ZNF443	10224	ENSG00000180855			Zfp709 (MGI:2384299)			
chr19	12600000	13800000	19p13.13			613638	"DEL19p13.13, C19DELp13.13, DUP19p13.13, C19DUPp13.13"	Chromosome 19p13.13 deletion syndrome (Chromosome 19p13.13 duplication syndrome)				contiguous gene syndrome	"Chromosome 19p13.13 deletion syndrome, 613638 (4); Chromosome 19p13.13 duplication syndrome, 613638 (4)"				
chr19	12600000	24200000	19p13.1-p12			603985	ZNF103	Zinc finger protein-103									
chr19	12600000	24200000	19p13.1-p12			603987	ZNF105	Zinc finger protein-105									
chr19	12600000	24200000	19p13.1-p12			603988	ZNF106	Zinc finger protein-106									
chr19	12600000	24200000	19p13.1-p12			603991	ZNF109	Zinc finger protein-109									
chr19	12600000	24200000	19p13.1-p12			603992	ZNF110	Zinc finger protein-110									
chr19	12600000	24200000	19p13.1-p12			603993	ZNF111	Zinc finger protein-111									
chr19	12600000	24200000	19p13.1-p12			603995	ZNF113	Zinc finger protein-113				?13q21					
chr19	12600000	24200000	19p13.1-p12			603997	ZNF118	Zinc finger protein-118				?13q21					
chr19	12600000	24200000	19p13.1-p12			603998	ZNF119	Zinc finger protein-119									
chr19	12600000	24200000	19p13.1-p12			603999	ZNF120	Zinc finger protein-120									
chr19	12600000	24200000	19p13.1-p12			604000	ZNF122	Zinc finger protein-122									
chr19	12600000	24200000	19p13.1-p12			603976	ZNF94	Zinc finger protein-94									
chr19	12646507	12666776	19cen-q12	19p13.13		609458	"MAN2B1, MANB"	"Mannosidase, alpha, class 2B, member 1"	MAN2B1	4125	ENSG00000104774		"Mannosidosis, alpha-, types I and II, 248500 (3), Autosomal recessive"	Man2b1 (MGI:107286)			
chr19	12666803	12675831	19p13.13	19p13.13		616850	"WDR83, MORG1"	WD repeat-containing protein 83	WDR83	84292	ENSG00000123154			Wdr83 (MGI:1915086)			
chr19	12671954	12681886	19p13.12-p13.11	19p13.13		600944	DHPS	Deoxyhypusine synthase	DHPS	1725	ENSG00000095059			Dhps (MGI:2683592)			
chr19	12688915	12696899	19p13.2	19p13.13		609074	"FBXW9, FBW9"	F-box and WD40 domain protein 9	FBXW9	84261	ENSG00000132004			Fbxw9 (MGI:1915878)			
chr19	12699193	12723995	19p13.13	19p13.13		603002	"TNPO2, TRN2, KPNB2B"	Transportin 2	TNPO2	30000	ENSG00000105576			Tnpo2 (MGI:2384849)			
chr19	12737458	12748323	19q13.3	19p13.13		601913	"ASNA1, ARSA1"	"arsA arsenite transporter, ATP-binding, E. coli, homolog of, 1"	ASNA1	439	ENSG00000198356			Asna1 (MGI:1928379)			
chr19	12751690	12758457	19p13.2-p13.12	19p13.13		607335	"BEST2, VMD2L1"	Bestrophin 2	BEST2	54831	ENSG00000039987			Best2 (MGI:2387588)			
chr19	12763001	12778483	19p13.13	19p13.13		607824	"HOOK2, HK2"	"Hook, Drosophila, homolog of, 2"	HOOK2	29911	ENSG00000095066			Hook2 (MGI:2181664)			
chr19	12791495	12793310	19p13.2	19p13.13		165161	JUNB	jun B proto-oncogene	JUNB	3726	ENSG00000171223			Junb (MGI:96647)			
chr19	12796819	12801909	19p13.2	19p13.13		600538	"PRDX2, PRX2, TDPX1, PTX1, NKEFB"	Peroxiredoxin 2	PRDX2	7001	ENSG00000167815	prev. mapped to chr.13		Prdx2 (MGI:109486)			
chr19	12802053	12813647	19p13.13	19p13.13		606034	"RNASEH2A, RNHIA, AGS4"	"Ribonuclease H2, large subunit"	RNASEH2A	10535	ENSG00000104889		"Aicardi-Goutieres syndrome 4, 610333 (3), Autosomal recessive"	Rnaseh2a (MGI:1916974)			
chr19	12825476	12835427	19p13	19p13.13		609553	RTBDN	Retbindin	RTBDN	83546	ENSG00000132026			Rtbdn (MGI:2443686)			
chr19	12833930	12874952	19p13.2	19p13.13		612256	"MAST1, SAST, KIAA0973"	Microtubule-associated serine/threonine kinase 1	MAST1	22983	ENSG00000105613			Mast1 (MGI:1861901)			
chr19	12875210	12881520	19p13.2-q13.4	19p13.13		126350	"DNASE2, DNL"	"Deoxyribonuclease II, lysosomal"	DNASE2	1777	ENSG00000105612			Dnase2a (MGI:1329019)			
chr19	12884421	12887202	19p13.13-p13.12	19p13.13		600599	"KLF1, EKLF, INLU, HBFQTL6, CDAN4"	"Kruppel-like factor 1, erythroid"	KLF1	10661	ENSG00000105610		"Blood group--Lutheran inhibitor, 111150 (3); Dyserythropoietic anemia, congenital, type IV, 613673 (3), Autosomal dominant; [Hereditary persistence of fetal hemoglobin], 613566 (3)"	Klf1 (MGI:1342771)			
chr19	12891128	12915344	19p13.2	19p13.13		608801	GCDH	Glutaryl-Coenzyme A dehydrogenase	GCDH	2639	ENSG00000105607		"Glutaricaciduria, type I, 231670 (3), Autosomal recessive"	Gcdh (MGI:104541)			
chr19	12898228	12919673	19p13.13	19p13.13		611487	"SYCE2, CESC1"	Synaptonemal complex central element protein 2	SYCE2	256126	ENSG00000161860			Syce2 (MGI:1919096)			
chr19	12938599	12944489	19p13.2	19p13.13		109091	"CALR, SSA"	Sicca syndrome antigen A (autoantigen Ro; calreticulin)	CALR	811	ENSG00000179218	"distal to C3, near LDLR"	"Myelofibrosis, somatic, 254450 (3); Thrombocythemia, somatic, 187950 (3)"	Calr (MGI:88252)			
chr19	12945813	12953642	19p13.2	19p13.13		600061	"RAD23A, HHR23A"	"RAD23, S. cerevisiae, homolog of, A"	RAD23A	5886	ENSG00000179262			Rad23a (MGI:105126)			
chr19	12954155	12957253	19p13.13	19p13.13		605162	"GADD45GIP1, PRG6, CRIF1"	Growth arrest- and DNA damage-inducible DABB45G-interacting protein	GADD45GIP1	90480	ENSG00000179271			Gadd45gip1 (MGI:1914947)			
chr19	12969617	12974752	19p13.2-p13.13	19p13.13		609068	"DAND5, CER2, CERL2, DANTE, COCO"	"DAN domain family, member 5"	DAND5	199699	ENSG00000179284			Dand5 (MGI:1344365)			
chr19	12995511	13098795	19p13.3	19p13.13		164005	"NFIX, NF1A, SOTOS2, MRSHSS"	Nuclear factor I/X (CCAAT-binding transcription factor)	NFIX	4784	ENSG00000008441		"Marshall-Smith syndrome, 602535 (3), Autosomal dominant; Sotos syndrome 2, 614753 (3), Autosomal dominant"	Nfix (MGI:97311)			
chr19	13097165	13103750	19p13.2-p13.1	19p13.13		151440	LYL1	Lymphoblastic leukemia derived sequence-1	LYL1	4066	ENSG00000104903		"Leukemia, T-cell acute lymphoblastoid, 151440 (2)"	Lyl1 (MGI:96891)			
chr19	13104899	13117566	19p13.3	19p13.13		611669	"TRMT1, TRM1"	"tRNA methyltransferase 1, S. cerevisiae, homolog of"	TRMT1	55621	ENSG00000104907			Trmt1 (MGI:1289155)			
chr19	13116847	13141146	19p13.13	19p13.13		610672	"NACC1, BTBD14B, NECFM"	"Nucleus accumbens-associated protein 1, BEN and BTB/POZ domains-containing"	NACC1	112939	ENSG00000160877		"Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination, 617393 (3), Autosomal dominant"	Nacc1 (MGI:1914080)			
chr19	13144057	13150373	19p13.2	19p13.13		603765	"STX10, SYN10"	Syntaxin 10	STX10	8677	ENSG00000104915						
chr19	13206441	13506459	19p13	19p13.13		601011	"CACNA1A, CACNL1A4, SCA6, EIEE42"	"Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit"	CACNA1A	773	ENSG00000141837		"Epileptic encephalopathy, early infantile, 42, 617106 (3), Autosomal dominant; Episodic ataxia, type 2, 108500 (3), Autosomal dominant; Migraine, familial hemiplegic, 1, 141500 (3), Autosomal dominant; Migraine, familial hemiplegic, 1, with progressive cerebellar ataxia, 141500 (3), Autosomal dominant; Spinocerebellar ataxia 6, 183086 (3), Autosomal dominant"	Cacna1a (MGI:109482)			
chr19	13764491	13774281	19p13.2	19p13.13		615105	"MRI1, MRDI"	"Methylthioribose-1-phosphate isomerase, S. cerevisiae, homolog of"	MRI1	84245	ENSG00000037757			Mri1 (MGI:1915123)			
chr19	13836286	13836358	19p13.12	19p13.12		610724	"MIR24-2, MIRN24-2"	Micro RNA 24-2	MIR24-2	407013							
chr19	13836439	13836516	19p13.12	19p13.12		612153	"MIR27, MIRN27A"	Micro RNA 27A	MIR27A	407018							
chr19	13836586	13836658	19p13.13	19p13.12		607962	"MIR23A, MIRN23A"	Micro RNA 23a	MIR23A	407010							
chr19	13862062	13880756	19p13.13	19p13.12		608229	"NANOS3, NOS3"	"Nanos, Drosophila, homolog of, 3"	NANOS3	342977	ENSG00000187556			Nanos3 (MGI:2675387)			
chr19	13874698	13874807	19p13.3	19p13.12		612746	"MIR181C, MIRN181C"	Micro RNA 181C	MIR181C	406957							
chr19	13906142	13930879	19p13.12	19p13.12		610055	"CC2D1A, MRT3"	Coiled-coil and C2 domain-containing 1A	CC2D1A	54862	ENSG00000132024		"Mental retardation, autosomal recessive 3, 608443 (3), Autosomal recessive"	Cc2d1a (MGI:2384831)			
chr19	13961529	14007513	19p13.1	19p13.12		600006	RFX1	Regulatory factor (trans-acting) 1 (influences HLA class II expression)	RFX1	5989	ENSG00000132005			Rfx1 (MGI:105982)			
chr19	14028147	14031557	19p13.3	19p13.12		606855	"RLN3, H3, RXN3"	Relaxin 3	RLN3	117579	ENSG00000171136			Rln3 (MGI:2158015)			
chr19	14031739	14052918	19p13.11	19p13.12		605350	"TCCR, WSX1"	T-cell cytokine receptor	IL27RA	9466	ENSG00000104998			Il27ra (MGI:1355318)			
chr19	14091687	14117746	19p13.1	19p13.12		601639	PRKACA	"Protein kinase, cAMP-dependent, catalytic, alpha"	PRKACA	5566	ENSG00000072062		"Cushing syndrome, ACTH-independent adrenal, somatic, 615830 (3)"	Prkaca (MGI:97592)			
chr19	14119508	14136627	19p13.13	19p13.12		609190	ASF1B	"Anti-silencing function 1, S. cerevisiae, homolog of, B"	ASF1B	55723	ENSG00000105011			Asf1b (MGI:1914179)			
chr19	14147736	14206244	19p13.3	19p13.12		616416	"ADGRL1, LPHN1, CIRL1, CL1, LEC2, KIAA0821"	Adhesion G protein-coupled receptor L1	ADGRL1	22859	ENSG00000072071			Adgrl1 (MGI:1929461)			
chr19	14381143	14408724	19p13.1	19p13.12		601211	"ADGRE5, CD97"	Adhesion G protein-coupled receptor E5	ADGRE5	976	ENSG00000123146			Adgre5 (MGI:1347095)			
chr19	14433353	14471866	19p12	19p13.12		601032	"PKN1, PRKCL1, PRK1, PAK1"	Protein kinase N1	PKN1	5585	ENSG00000123143			Pkn1 (MGI:108022)			
chr19	14472465	14475361	19p13.1	19p13.12		176802	PTGER1	"Prostaglandin E receptor 1, EP1 subtype, 42kD"	PTGER1	5731	ENSG00000160951			Ptger1 (MGI:97793)			
chr19	14477758	14496148	19p13.1	19p13.12		605072	"RGS19IP1, C19orf3, GIPC"	Regulator of G-protein signaling 19 interacting protein 1	GIPC1	10755	ENSG00000123159			Gipc1 (MGI:1926252)			
chr19	14514763	14530596	19p13.2	19p13.12		604572	"DNAJB1, HSPF1"	"DnaJ, E. coli, homolog of, subfamily B, member 1 (heat-shock 40kD protein 1)"	DNAJB1	3337	ENSG00000132002			Dnajb1 (MGI:1931874)			
chr19	14527751	14565979	19p13.12	19p13.12		610057	"TECR, GPSN2, TER, SC2, MRT14"	"Trans-2,3-enoyl-CoA reductase"	TECR	9524	ENSG00000099797		"Mental retardation, autosomal recessive 14, 614020 (3), Autosomal recessive"	Tecr (MGI:1915408)			
chr19	14566077	14572076	19p13.12-p13.11	19p13.12		603842	NDUFB7	"NADH-ubiquinone oxidoreductase 1 beta subcomplex, 7"	NDUFB7	4713	ENSG00000099795			Ndufb7 (MGI:1914166)			
chr19	14580776	14612026	19p13.12	19p13.12		616838	CLEC17A	"C-type lectin domain family 17, member A"	CLEC17A	388512	ENSG00000187912						
chr19	14600174	14674917	19p13.1	19p13.12		606101	EMR3	"EGF-like module-containing, mucin-like hormone receptor 3"	ADGRE3	84658	ENSG00000131355						
chr19	14689786	14733745	19p13.1	19p13.12		611811	"ZNF333, KIAA1806"	Zinc finger protein 333	ZNF333	84449	ENSG00000160961						
chr19	14732696	14778540	19p13.1	19p13.12		606100	"ADGRE2, EMR2, VBU"	Adhesion G protein-coupled receptor E2	ADGRE2	30817	ENSG00000127507		"Vibratory urticaria, 125630 (3), Autosomal dominant"				
chr19	14950032	15010642	19p13.12	19p13.12		600637	"SLC1A6, EAAT4"	"Solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6"	SLC1A6	6511	ENSG00000105143			Slc1a6 (MGI:1096331)			
chr19	15049479	15058292	19p13.1	19p13.12		605848	"CASP14, ARCI12"	"Caspase 14, apoptosis-related cysteine protease"	CASP14	23581	ENSG00000105141		"Ichthyosis, congenital, autosomal recessive 12, 617320 (3), Autosomal recessive"	Casp14 (MGI:1335092)			
chr19	15107363	15114987	19p13.12	19p13.12		617377	SYDE1	"Synapse defective Rho GTPase, C. elegans, homolog of, 1"	SYDE1	85360	ENSG00000105137			Syde1 (MGI:1918959)			
chr19	15114973	15125798	19p13.1	19p13.12		605770	"ILVBL, AHAS"	"IlvB-like (acetolactate synthase, bacterial, homolog of)"	ILVBL	10994	ENSG00000105135			Ilvbl (MGI:1351911)			
chr19	15159632	15200980	19p13.2-p13.1	19p13.12		600276	"NOTCH3, CADASIL1, CASIL, IMF2, LMNS"	"Notch, Drosophila, homolog of, 3"	NOTCH3	4854	ENSG00000074181	mutation identified in 1 IMF2 family	"Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1, 125310 (3), Autosomal dominant; Lateral meningocele syndrome, 130720 (3), Autosomal dominant; ?Myofibromatosis, infantile 2, 615293 (3), Autosomal dominant"	Notch3 (MGI:99460)			
chr19	15226918	15233452	19p13.12	19p13.12		617400	"EPHX3, ABHD9"	Epoxide hydrolase 3	EPHX3	79852	ENSG00000105131			Ephx3 (MGI:1919182)			
chr19	15236835	15332542	19p13.1	19p13.12		608749	"BRD4, CAP, HUNK1"	Bromodomain-containing protein 4	BRD4	23476	ENSG00000141867	fused with NUT					
chr19	15353520	15379814	19p13.12	19p13.12		604692	"AKAP8, AKAP95"	A-kinase anchor protein 8	AKAP8	10270	ENSG00000105127			Akap8 (MGI:1928488)			
chr19	15380047	15419120	19p13.12-p13.11	19p13.12		609475	"AKAP8L, HA95, NAKAP, HAP95"	A-kinase anchor protein 8-like protein	AKAP8L	26993	ENSG00000011243			Akap8l (MGI:1860606)			
chr19	15451623	15464580	19p13.12	19p13.12		616561	RASAL3	Ras protein activator-like 3	RASAL3	64926	ENSG00000105122			Rasal3 (MGI:2444128)			
chr19	15468644	15479503	19p13.12	19p13.12		608199	PGRPL	"Peptidoglycan recognition protein, long"	PGLYRP2	114770	ENSG00000161031			Pglyrp2 (MGI:1928099)			
chr19	15508486	15552316	19p13.12	19p13.12		611495	"CYP4F22, ARCI5, LI3"	"Cytochrome P450, family 4, subfamily F, polypeptide 22"	CYP4F22	126410	ENSG00000171954		"Ichthyosis, congenital, autosomal recessive 5, 604777 (3), Autosomal recessive"	Cyp4f39 (MGI:2445210)			
chr19	15615206	15629637	19p13.1	19p13.12		611545	CYP4F8	"Cytochrome P450, family 4, subfamily F, polypeptide 8"	CYP4F8	11283	ENSG00000186526			Cyp4f15 (MGI:2146921)			
chr19	15640896	15661605	19p13.2	19p13.12		601270	"CYP4F3, LTB4H"	"Cytochrome P450, subfamily IVF, polypeptide 3"	CYP4F3	4051	ENSG00000186529			Cyp4f13 (MGI:2158641)			
chr19	15673017	15698818	19p13.1	19p13.12		611485	CYP4F12	"Cytochrome P450, family 4, subfamily F, polypeptide 12"	CYP4F12	66002	ENSG00000186204			Cyp4f14 (MGI:1927669)			
chr19	15828946	15836320	19p13.12	19p13.12		617500	"UCA1, LINC00178, CUDR"	Urothelial cancer-associated gene 1	UCA1	652995							
chr19	15878023	15898119	19p13.12	19p13.12		604426	CYP4F2	"Cytochrome P450, family 4, subfamily F, polypeptide 2"	CYP4F2	8529	ENSG00000186115			Cyp4f18 (MGI:1919304)			
chr19	15912369	15934865	19p13.1	19p13.12		611517	CYP4F11	"Cytochrome P450, family 4, subfamily F, polypeptide 11"	CYP4F11	57834	ENSG00000171903			Cyp4f40 (MGI:3645508)			
chr19	16067506	16103004	19p13.1	19p13.12-p13.11		600317	TPM4	Tropomyosin 4	TPM4	7171	ENSG00000167460						
chr19	16111679	16133634	19p13.2-cen	19p13.11		165040	"RAB8A, MEL"	Ras-associated protein RAB8A (oncogene MEL)	RAB8A	4218	ENSG00000167461			Rab8a (MGI:96960)			
chr19	16185183	16192045	19p13.12	19p13.11		614554	"FAM32A, OTAG12"	"Family with sequence similarity 32, member A"	FAM32A	26017	ENSG00000105058			Fam32a (MGI:1915172)			
chr19	16197853	16235344	19p13.12	19p13.11		603535	"AP1M1, AP47, CLAPM2"	"Adaptor-related protein complex 1, mu 1 subunit"	AP1M1	8907	ENSG00000072958			Ap1m1 (MGI:102776)			
chr19	16324825	16328661	19p13.1	19p13.11		602016	"KLF2, LKLF"	Kruppel-like factor 2	KLF2	10365	ENSG00000127528			Klf2 (MGI:1342772)			
chr19	16355243	16472011	19p13.11	19p13.11		616826	"EPS15L1, EPS15R"	EPS15-like protein 1	EPS15L1	58513	ENSG00000127527			Eps15l1 (MGI:104582)			
chr19	16479056	16496191	19p13.12	19p13.11		611414	"CALR3, CRT2, CMH19"	Calreticulin 3	CALR3	125972	ENSG00000269058	mutation identified in 1 CMH19 patient	"?Cardiomyopathy, hypertrophic, 19, 613875 (3), Autosomal dominant"	Calr3 (MGI:1920566)			
chr19	16574906	16628203	19p13.11	19p13.11		605043	"MED26, CRSP7, CRSP70"	Mediator complex subunit 26	MED26	9441	ENSG00000105085			Med26 (MGI:1917875)			
chr19	16661126	16689019	19p13.11	19p13.11		611235	"TMEM38A, TRICA"	Transmembrane protein 38A	TMEM38A	79041	ENSG00000072954			Tmem38a (MGI:1921416)			
chr19	16719525	16817962	19p13.11	19p13.11		616250	NWD1	NACHT domain- and WD repeat-containing protein 1	NWD1	284434	ENSG00000188039			Nwd1 (MGI:2442268)			
chr19	16829386	16880354	19p13.11	19p13.11		607777	"SIN3B, KIAA0700"	"Sin3, yeast, homolog of, B"	SIN3B	23309	ENSG00000127511			Sin3b (MGI:107158)			
chr19	16888859	16892599	19p12	19p13.11		602779	"F2RL3, PAR4"	"Coagulation factor II, thrombin, receptor-like 3 (protease-activated receptor-4)"	F2RL3	9002	ENSG00000127533			F2rl3 (MGI:1298207)			
chr19	16892946	17026817	19p13.11	19p13.11		608841	"CPAMD8, KIAA1283, ASGD8"	Complement component 3- and pregnancy zone protein-like alpha-2-macroglobin domain-containing protein 8	CPAMD8	27151	ENSG00000160111		"Anterior segment dysgenesis 8, 617319 (3), Autosomal recessive"				
chr19	17049760	17075605	19p13.11	19p13.11		613434	"HAUS8, DGT4, HICE1"	"HAUS augmin-like complex, subunit 8"	HAUS8	93323	ENSG00000131351			Haus8 (MGI:1923728)			
chr19	17075780	17213294	19p13.1	19p13.11		602129	"MYO9B, MYR5, CELIAC4"	Myosin IXB	MYO9B	4650	ENSG00000099331		"{Celiac disease, susceptibility to, 4}, 609753 (3)"	Myo9b (MGI:106624)			
chr19	17231884	17245341	19p13.1	19p13.11		132880	"NR2F6, ERBAL2, EAR2"	"Nuclear receptor subfamily 2, group F, member 6"	NR2F6	2063	ENSG00000160113			Nr2f6 (MGI:1352453)			
chr19	17250020	17264795	19p13.1	19p13.11		611810	"USHBP1, MCC2"	USH1C-binding protein 1	USHBP1	83878	ENSG00000130307			Ushbp1 (MGI:1922920)			
chr19	17267375	17279352	19p13.11	19p13.11		612766	"C10orf62, MERIT40, NBA1"	Chromosome 19 open reading frame 62	BABAM1	29086	ENSG00000105393			Babam1 (MGI:1915501)			
chr19	17302806	17306842	19p13.1	19p13.11		611840	MRPL34	Mitochondrial ribosomal protein L34	MRPL34	64981	ENSG00000130312			Mrpl34 (MGI:2137227)			
chr19	17323222	17334833	19p13.11	19p13.11		610216	"TMEM16H, KIAA1623"	Transmembrane protein 16H	ANO8	57719	ENSG00000074855			Ano8 (MGI:2687327)			
chr19	17334981	17342730	19p13.11	19p13.11		608536	"GTPBP3, MSS1, COXPD23"	GTP-binding protein 3	GTPBP3	84705	ENSG00000130299		"Combined oxidative phosphorylation deficiency 23, 616198 (3), Autosomal recessive"	Gtpbp3 (MGI:1917609)			
chr19	17351447	17377348	19p13.2	19p13.11		607647	"PLVAP, PV1"	Plasmalemma vesicle-associated protein	PLVAP	83483	ENSG00000130300			Plvap (MGI:1890497)			
chr19	17402938	17405647	19p13.2	19p13.11		600534	BST2	Bone marrow stromal cell antigen	BST2	684	ENSG00000130303						
chr19	17455424	17460915	19p13.11	19p13.11		608791	"NXNL1, RDCVF, TXNL6, LOC115861"	Nucleoredoxin-like protein 1	NXNL1	115861	ENSG00000171773			Nxnl1 (MGI:1924446)			
chr19	17468744	17506168	19p13.1	19p13.11		600691	"SLC27A1, FATP, FATP1"	"Solute carrier family 27, member 1"	SLC27A1	376497	ENSG00000130304			Slc27a1 (MGI:1347098)			
chr19	17511622	17521290	19p13.2	19p13.11		604951	PGLS	6-phosphogluconolactonase	PGLS	25796	ENSG00000130313			Pgls (MGI:1913421)			
chr19	17523300	17556754	19p13.11	19p13.11		609967	BCNP1	B-cell novel protein 1	FAM129C	199786	ENSG00000167483			Fam129c (MGI:3686743)			
chr19	17555593	17583161	19p13.11	19p13.11		617531	"COLGALT1, GLT25D1"	Collagen beta(1-0)galactosyltransferase 1	COLGALT1	79709	ENSG00000130309			Colgalt1 (MGI:1924348)			
chr19	17601327	17688343	19p13.3	19p13.11		609894	"UNC13A, KIAA1032"	"UNC13, C. elegans, homolog of, A"	UNC13A	23025	ENSG00000130477			Unc13a (MGI:3051532)			
chr19	17719451	17734514	19p13.11	19p13.11		607573	"MAP1S, BPY2IP1, VCY2IP1, C19orf5"	Microtubule-associated protein 1S	MAP1S	55201	ENSG00000130479			Map1s (MGI:2443304)			
chr19	17747717	17788567	19p13.11	19p13.11		613437	FCHO1	FCH domain-only protein 1	FCHO1	23149	ENSG00000130475			Fcho1 (MGI:1921265)			
chr19	17794827	17813575	19p	19p13.11		605863	"TMEM3, B3GNT3"	"Transmembrane protein 3 (beta-1,3-N-acetylglucosaminyltransferase 3)"	B3GNT3	10331	ENSG00000179913			B3gnt3 (MGI:2152535)			
chr19	17816512	17821573	19p13.2	19p13.11		146738	INSL3	"Insulin-like 3, Leydig cell"	INSL3	3640	ENSG00000248099		"Cryptorchidism, 219050 (3), Autosomal dominant"	Insl3 (MGI:108427)			
chr19	17824781	17848070	19p13.1	19p13.11		600173	"JAK3, JAKL"	"Janus kinase 3 (Janus kinase, leukocyte)"	JAK3	3718	ENSG00000105639		"SCID, autosomal recessive, T-negative/B-positive type, 600802 (3), Autosomal recessive"	Jak3 (MGI:99928)			
chr19	17859877	17863323	19p	19p13.11		604178	RPL18A	Ribosomal protein L18a	RPL18A	6142	ENSG00000105640			Rpl18a (MGI:1924058)			
chr19	17871393	17895174	19p13.2-p12	19p13.11		601843	"SLC5A5, NIS, TDH1"	"Solute carrier family 5 (sodium iodide symporter), member-5"	SLC5A5	6528	ENSG00000105641		"Thyroid dyshormonogenesis 1, 274400 (3), Autosomal recessive"	Slc5a5 (MGI:2149330)			
chr19	18058993	18099026	19p13.1	19p13.11		601604	"IL12RB1, IMD30"	"Interleukin-12 receptor, beta-1"	IL12RB1	3594	ENSG00000096996		"Immunodeficiency 30, 614891 (3), Autosomal recessive"	Il12rb1 (MGI:104579)			
chr19	18097763	18151691	19p13.11	19p13.11		612258	"MAST3, KIAA0561"	Microtubule-associated serine/threonine kinase 3	MAST3	23031	ENSG00000099308			Mast3 (MGI:2683541)			
chr19	18153177	18170532	19q13.2-q13.4	19p13.11		603157	"PIK3R2, MPPH1"	"Phosphatidylinositol 3-kinase, regulatory subunit 2"	PIK3R2	5296	ENSG00000105647		"Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1, 603387 (3), Autosomal dominant"	Pik3r2 (MGI:1098772)			
chr19	18173779	18178123	19p13.11	19p13.11		604664	"IFI30, GILT"	Interferon-gamma-inducible protein 30	IFI30	10437	ENSG00000216490			Ifi30 (MGI:2137648)			
chr19	18193229	18196741	19p13.11	19p13.11		616133	MPV17L2	MPV17-like protein 2	MPV17L2	84769	ENSG00000254858			Mpv17l2 (MGI:2681846)			
chr19	18196783	18204063	19p13.1-p12	19p13.11		179490	RAB3A	RAS-associated protein RAB3A	RAB3A	5864	ENSG00000105649			Rab3a (MGI:97843)			
chr19	18207960	18248199	19p13.1	19p13.11		600128	"PDE4C, DPDE1"	"Phosphodiesterase-4C, cAMP-specific (dunce, Drosophila, homolog phosphodiesterase E1)"	PDE4C	5143	ENSG00000285188	between JUND (proximal) and RAB3A (distal)		Pde4c (MGI:99556)			
chr19	18279693	18281655	19p13.1-p12	19p13.11		165162	JUND	jun D proto-oncogene	JUND	3727	ENSG00000130522			Jund (MGI:96648)			
chr19	18306229	18323190	19p13.11	19p13.11		607284	LSM4	LSM4 protein	LSM4	25804	ENSG00000130520			Lsm4 (MGI:1354692)			
chr19	18340572	18369952	19p13.11	19p13.11		610694	"PGPEP1, PCP, PGP"	Pyroglutamyl peptidase I	PGPEP1	54858	ENSG00000130517			Pgpep1 (MGI:1913772)			
chr19	18382169	18389176	19p13.2-p13.1	19p13.11		605312	"GDF15, PLAB, PDF, MIC1"	"Growth/differentiation factor-15 (bone morphogenetic protein, placental)"	GDF15	9518	ENSG00000130513			Gdf15 (MGI:1346047)			
chr19	18391136	18397644	19p13.2-p12	19p13.11		607518	"LRRC25, MAPA"	Leucine rich repeat containing 25	LRRC25	126364	ENSG00000175489			Lrrc25 (MGI:2445284)			
chr19	18418718	18434561	19p13.1	19p13.11		607391	SSBP4	Single-stranded DNA-binding protein 4	SSBP4	170463	ENSG00000130511			Ssbp4 (MGI:1924150)			
chr19	18434387	18438648	19p13.1	19p13.11		611670	"ISYNA1, IPS"	Myoinositol 1-phosphate synthase A1	ISYNA1	51477	ENSG00000105655	pseudogene on 4p15		Isyna1 (MGI:1919030)			
chr19	18442662	18522126	19p13.1	19p13.11		600284	ELL	ELL gene (11-19 lysine-rich leukemia gene)	ELL	8178	ENSG00000105656			Ell (MGI:109377)			
chr19	18531751	18544076	19p12	19p13.11		604840	"FKBP8, FKBP38"	FK506-binding protein 8	FKBP8	23770	ENSG00000105701	pseudogene on 1q32		Fkbp8 (MGI:1341070)			
chr19	18557761	18569386	19p13.11	19p13.11		615178	"KXD1, C10orf50"	KXDL motif-containing protein 1	KXD1	79036	ENSG00000105700			Kxd1 (MGI:1922870)			
chr19	18563765	18577459	19p13.1-p12	19p13.11		191321	UBA52	Ubiquitin A-52 residue ribosomal protein fusion product 1	UBA52	7311	ENSG00000221983			Uba52-ps (MGI:3644625)			
chr19	18593224	18606849	19p12	19p13.11		604237	"CRLF1, CISS1"	Cytokine-like factor 1	CRLF1	9244	ENSG00000006016		"Cold-induced sweating syndrome 1, 272430 (3), Autosomal recessive"	Crlf1 (MGI:1340030)			
chr19	18612871	18621039	19p12	19p13.11		617096	"TMEM59L, BSMAP"	Transmembrane protein 59-like	TMEM59L	25789	ENSG00000105696			Tmem59l (MGI:1915187)			
chr19	18683614	18782332	19p13	19p13.11		607536	"CRTC1, MECT1, KIAA0616, FLJ14027"	CREB-regulated transcription coactivator 1	CRTC1	23373	ENSG00000105662	t(11;19)	Mucoepidermoid salivary gland carcinoma (3)	Crtc1 (MGI:2142523)			
chr19	18782772	18791304	19p13.1	19p13.11		600310	"COMP, EDM1, MED, PSACH"	Cartilage oligomeric matrix protein	COMP	1311	ENSG00000105664		"Epiphyseal dysplasia, multiple, 1, 132400 (3), Autosomal dominant; Pseudoachondroplasia, 177170 (3), Autosomal dominant"	Comp (MGI:88469)			
chr19	18831404	18868231	19p13.2-p13.11	19p13.11		601430	"UPF1, RENT1, HUPF1"	"Upf1, yeast, homolog of"	UPF1	5976	ENSG00000005007			Upf1 (MGI:107995)			
chr19	18868545	18896726	19p12	19p13.11		606919	"CERS1, LASS1, UOG1, EPM8"	Ceramide synthase 1	CERS1	10715	ENSG00000223802	mutation identified in 1 EPM8 family	"?Epilepsy, progressive myoclonic, 8, 616230 (3), Autosomal recessive"	Cers1 (MGI:2136690)			
chr19	18868545	18896143	19p12	19p13.11		602880	"GDF1, DTGA3, DORV, RAI"	Growth/differentiation factor 1	GDF1	2657	ENSG00000223802		"Double-outlet right ventricle, 217095 (3); Right atrial isomerism, 208530 (3), Autosomal recessive; Tetralogy of Fallot, 187500 (3), Autosomal dominant; Transposition of great arteries, dextro-looped 3, 613854 (3), Autosomal dominant"	Gdf1 (MGI:95683)			
chr19	18899510	18919402	19p13.11	19p13.11		606942	COPE	"Cotamer protein complex, subunit epsilon"	COPE	11316	ENSG00000105669			Cope (MGI:1891702)			
chr19	18929200	18941257	19p13.11	19p13.11		604800	HOMER3	"Homer, homolog 3 (Drosophila)"	HOMER3	9454	ENSG00000051128			Homer3 (MGI:1347359)			
chr19	18990886	19034051	19p13.11	19p13.11		607993	"SUGP2, SRFS14, KIAA0365"	SURP and G-patch domains-containing protein 2	SUGP2	10147	ENSG00000064607			Sugp2 (MGI:2678085)			
chr19	19063960	19113029	19p13.11	19p13.11		610823	SLC25A42	"Solute carrier family 25, member 42"	SLC25A42	284439	ENSG00000181035			Slc25a42 (MGI:1920345)			
chr19	19145566	19170288	19p12	19p13.11		600661	MEF2B	"MADS box transcription enhancer factor 2, polypeptide B (myocyte enhancer factor 2B)"	MEF2B	100271849	ENSG00000213999			Mef2b (MGI:104526)			
chr19	19176903	19192590	19p13.11	19p13.11		616601	"BORCS8, MEF2BNB"	"BLOC1-related complex, subunit 8"	BORCS8	729991	ENSG00000254901			Borcs8 (MGI:1919618)			
chr19	19192198	19201868	19p12	19p13.11		603200	RFXANK	"Regulatory factor X, ankyrin repeat-containing"	RFXANK	8625	ENSG00000064490		"MHC class II deficiency, complementation group B, 209920 (3), Autosomal recessive"	Rfxank (MGI:1333865)			
chr19	19211972	19252251	19p12	19p13.11		600826	"CSPG3, NCAN"	Chondroitin sulfate proteoglycan 3 (neurocan)	NCAN	1463	ENSG00000130287			Ncan (MGI:104694)			
chr19	19264364	19273264	19p12	19p13.11		606563	"TM6SF2, KIAA1926"	"Transmembrane 6 superfamily, member 2"	TM6SF2	53345	ENSG00000213996			Tm6sf2 (MGI:1933210)			
chr19	19276512	19320511	19p13.11	19p13.11		607992	"SUGP1, SF4"	SURP and G-patch domains-containing protein 1	SUGP1	57794	ENSG00000105705			Sugp1 (MGI:1917866)			
chr19	19320606	19358753	19p13.11	19p13.11		614560	"MAU2, SCC4, KIAA0892"	"MAU2 chromatid cohesion factor, C. elegans, homolog of"	MAU2	23383	ENSG00000129933			Mau2 (MGI:1921799)			
chr19	19385802	19508931	19q13.11	19p13.11		614997	GATAD2A	GATA zinc finger domain-containing protein 2A	GATAD2A	54815	ENSG00000167491			Gatad2a (MGI:2384585)			
chr19	19514218	19515659	19p13.11	19p13.11		610712	"TSSK6, SSTK, TSSK4"	Testis-specific serine/threonine kinase 6	TSSK6	83983	ENSG00000178093			Tssk6 (MGI:2148775)			
chr19	19516209	19528203	19p13.2-p13.1	19p13.11		609435	"NDUFA13, GRIM19"	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 13"	NDUFA13	51079	ENSG00000186010		"{Thyroid carcinoma, Hurthle cell}, 607464 (3)"	Ndufa13 (MGI:1914434)			
chr19	19538264	19546658	19p13.11	19p13.11		612419	CILP2	Cartilage intermediate layer protein 2	CILP2	148113	ENSG00000160161			Cilp2 (MGI:1915959)			
chr19	19561706	19618915	19p13.11	19p13.11		608127	PBX4	Pre-B-cell leukemia transcription factor 4	PBX4	80714	ENSG00000105717			Pbx4 (MGI:1931321)			
chr19	19623654	19628394	19p12	19p13.11		605110	"LPAR2, EDG4"	Lysophosphatidic acid receptor 2	LPAR2	9170	ENSG00000064547			Lpar2 (MGI:1858422)			
chr19	19629472	19643666	19p12-p11	19p13.11		609694	GMIP	GEM-interacting protein	GMIP	51291	ENSG00000089639			Gmip (MGI:1926066)			
chr19	19668069	19683505	19p13.1-p12	19p13.11		603983	ZNF101	Zinc finger protein-101	ZNF101	94039	ENSG00000181896						
chr19	19710471	19733111	19p13.3-p13.2	19p13.11		194556	"ZNF14, KOX6"	Zinc finger protein-14 (KOX 6)	ZNF14	7561	ENSG00000105708			"Zfp976,Zfp975 (MGI:3648690,MGI:3036263)"			
chr19	19756370	19776412	19p13.11	19p13.11		617117	LINC00663	Long intergenic noncoding RNA 663	LINC00663	284440							
chr19	19865829	19893483	19p13	19p13.11		606954	ZNF253	Zinc finger protein 253	ZNF253	56242	ENSG00000256771			Zfp65 (MGI:107769)			
chr19	19900912	19935572	19p13.1-p12	19p12		603975	ZNF93	Zinc finger protein-93	ZNF93	81931	ENSG00000184635			Zfp457 (MGI:2664334)			
chr19	20077993	20127089	19p13.1-p12	19p12		603973	ZNF90	Zinc finger protein-90	ZNF90	7643	ENSG00000213988						
chr19	20531229	20565820	19p13.1-p12	19p12		603984	"ZNF737, ZNF102"	Zinc finger protein-737	ZNF737	100129842	ENSG00000237440						
chr19	20923226	20950696	19p13.1-p12	19p12		603899	ZNF85	Zinc finger protein-85	ZNF85	7639	ENSG00000105750						
chr19	21724040	21767627	19p13.1-p12	19p12		603982	ZNF100	Zinc finger protein-100	ZNF100	163227	ENSG00000197020						
chr19	21804948	21852094	19p13.1-p12	19p12		603972	ZNF43	Zinc finger protein-43	ZNF43	7594	ENSG00000198521			Zfp458 (MGI:3040691)			
chr19	21939765	22010942	19p13.1-p12	19p12		603977	"ZNF208, ZNF95"	Zinc finger protein-208	ZNF208	7757	ENSG00000160321			Zfp619 (MGI:1917477)			
chr19	22052447	22091102	19p12	19p12		606957	ZNF257	Zinc finger protein 257	ZNF257	113835	ENSG00000197134						
chr19	22391096	22422345	19p12	19p12		603980	ZNF98	Zinc finger protein-98	ZNF98	148198	ENSG00000197360						
chr19	22752182	22784170	19p12	19p12		603981	ZNF99	Zinc finger protein-99	ZNF99	7652	ENSG00000213973						
chr19	23305003	23395559	19p13.1-p12	19p12		603971	ZNF91	Zinc finger protein-91	ZNF91	7644	ENSG00000167232			Zfp869 (MGI:1914119)			
chr19	24033404	24129967	19p13.12-p13.11	19p12		604768	"ZNF254, ZNF91L"	Zinc finger protein-254	ZNF254	9534	ENSG00000213096						
chr19	26200000	58617616	19q			601764	"BFIS1, BFIC1"	Benign familial infantile seizures		8181			"Seizures, benign familial infantile, 1, 601764 (2), Autosomal dominant"				
chr19	26200000	58617616	19q			607592	HPCQTL19	Prostate cancer aggressiveness quantitative trait locus on chromosome 19		347747		D19S902	"{Prostate cancer aggressiveness QTL}, 176807 (2), Autosomal dominant"				
chr19	26200000	58617616	19q			606712	SLI2	"Specific language impairment QTL, 2"		171014			"Specific language impairment QTL, 2, 606712 (2), Multifactorial"				
chr19	28100000	31900000	19q12			606875	HSCR7	"Hirschsprung disease, susceptibility to, 7"		246322			"{Hirschsprung disease, susceptibility to, 7}, 606875 (2)"				
chr19	29207259	29213228	19q12	19q12		191327	UQCRFS1	"Ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1"	UQCRFS1	7386	ENSG00000169021			Uqcrfs1 (MGI:1913944)			
chr19	29606262	29617254	19q12	19q12		606114	"RPP29, POP4"	"Ribonuclease P, 29kD subunit"	POP4	10775	ENSG00000105171			Pop4 (MGI:1913411)			
chr19	29665419	29675476	19q11	19q12		615200	"PLEKHF1, LAPF, PHAFIN1"	"Pleckstrin homolog domain-containing protein, family F, member 1"	PLEKHF1	79156	ENSG00000166289			Plekhf1 (MGI:1919537)			
chr19	29698885	29715788	19q12	19q12		614297	"C19orf12, NBIA4, SPG43"	Chromosome 19 open reading frame 12	C19orf12	83636	ENSG00000131943	mutation identified in 1 SPG43 family	"Neurodegeneration with brain iron accumulation 4, 614298 (3), Autosomal recessive; ?Spastic paraplegia 43, autosomal recessive, 615043 (3), Autosomal recessive"	1600014C10Rik (MGI:1919494)			
chr19	29811993	29824316	19q13.1	19q12		123837	CCNE1	Cyclin E1	CCNE1	898	ENSG00000105173			Ccne1 (MGI:88316)			
chr19	29923643	30016611	19q12	19q12		603494	"URI1, NNX3, RMP"	Prefoldin-like chaperone URI1	URI1	8725	ENSG00000105176			Uri1 (MGI:1342294)			
chr19	31149869	31349524	19q13.11	19q12		614119	"TSHZ3, KIAA1474"	Teashirt zinc finger homeobox 3	TSHZ3	57616	ENSG00000121297			Tshz3 (MGI:2442819)			
chr19	31900000	58617616	19q13			100070	"AAA1, AAA"	"Aortic aneurysm, familial abdominal 1"		100329167		near D19S416	"Aortic aneurysm, familial abdominal 1, 100070 (2), Autosomal dominant"				
chr19	31900000	58617616	19q13			608542	ANIB2	"Aneurysm, intracranial berry, 2"	ANIB2	449013		between D19S245 and D19S246	"Aneurysm, intracranial berry, 2, 608542 (2)"				
chr19	31900000	58617616	19q13			609376	"CTRCT35, CATCN1"	Cataract 35		619404		max lod at D19S416	"Cataract 35, congenital nuclear, 609376 (2), Autosomal recessive"				
chr19	31900000	35100000	19q13.11			613026	"DEL19q13.11d, C19DELq13.11d"	"Chromosome 19q13.11 deletion syndrome, distal"				contiguous gene syndrome	"Chromosome 19q13.11 deletion syndrome, distal, 613026 (4), Autosomal dominant"				
chr19	31900000	35100000	19q13.11			617219	"DEL19q13.11p, C19DELq13.11p"	"Chromosome 19q13.11 deletion syndrome, proximal"					"Chromosome 19q13.11 deletion syndrome, proximal, 617219 (4), Autosomal dominant"				
chr19	31900000	58617616	19q13.1-qter			129150	E11S	Echo 11 sensitivity	E11S	1878							
chr19	31900000	58617616	19q13			611907	EA7	"Episodic ataxia, type 7"		100188859		between rs1366444 and rs952108	"Episodic ataxia, type 7, 611907 (2), Autosomal dominant"				
chr19	31900000	58617616	19q13			600757	OFC3	Orofacial cleft-3	OFC3	4965		?role of BCL3	"Orofacial cleft-3, 600757 (2), ?Autosomal dominant"				
chr19	31900000	35100000	19q13.11			617932	RHPN2	Rhophilin 2									
chr19	31900000	58617616	19q13			614746	UAQTL5	"Uric acid concentration, serum, quantitative trait locus 5"		100996934		associated with rs150414818	"[Uric acid concentration, serum, QTL5], 614746 (2)"				
chr19	32405748	32485892	19q13.11	19q13.11		613894	DPY19L3	DPY19-like 3	DPY19L3	147991	ENSG00000178904			Dpy19l3 (MGI:2443952)			
chr19	32581187	32587451	19q13.11	19q13.11		604583	"PDCD5, TFAR19"	Programmed cell death 5	PDCD5	9141	ENSG00000105185			"Pdcd5,Pdcd5-ps (MGI:3782009,MGI:1913538)"			
chr19	32675406	32678299	19q13.11	19q13.11		607814	"RGS9BP, R9AP, RGS9, PERRS"	Regulator of G protein signaling 9-binding protein	RGS9BP	388531	ENSG00000186326		"Bradyopsia, 608415 (3)"	Rgs9bp (MGI:2384418)			
chr19	32830510	32870956	19q13.1	19q13.11		604144	"SLC7A9, CSNU3"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 9"	SLC7A9	11136	ENSG00000021488		"Cystinuria, 220100 (3), Autosomal recessive, Autosomal dominant"	Slc7a9 (MGI:1353656)			
chr19	32875924	32972028	19q13.11	19q13.11		615470	"CEP89, CCDC123, CEP123, FLJ14640"	"Centrosomal protein, 89kD"	CEP89	84902	ENSG00000121289			Cep89 (MGI:1919390)			
chr19	32972211	32977494	19q13.11	19q13.11		610884	"C19orf40, FAAP24"	"Chromosome 19 open reading frame 40 (Fanconi anemia-associated protein, 24kD"	FAAP24	91442	ENSG00000131944			Faap24 (MGI:2142208)			
chr19	33194692	33208866	19q12-q13.2	19q13.11		603159	LRP3	Low density lipoprotein receptor related protein 3	LRP3	4037	ENSG00000130881			Lrp3 (MGI:3584516)			
chr19	33208663	33225849	19q13.11	19q13.11		607959	"SLC7A10, ASC1"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 10"	SLC7A10	56301	ENSG00000130876			Slc7a10 (MGI:1858261)			
chr19	33299933	33302563	19q13.1	19q13.11		116897	"CEBPA, CEBP"	"CCAAT/enhancer-binding protein (C/EBP), alpha"	CEBPA	1050	ENSG00000245848	germline mutation identified in 1 AML family	"?Leukemia, acute myeloid, 601626 (3), Autosomal dominant; Leukemia, acute myeloid, somatic, 601626 (3)"	Cebpa (MGI:99480)			
chr19	33373668	33382685	19q13.11	19q13.11		138972	"CEBPG, GPE1BP"	"CCAAT/enhancer-binding protein, gamma"	CEBPG	1054	ENSG00000153879			Cebpg (MGI:104982)			
chr19	33386948	33521892	19cen-q13.11	19q13.11		613230	PEPD	Peptidase D (prolidase)	PEPD	5184	ENSG00000124299	closely linked to APOC2	"Prolidase deficiency, 170100 (3), Autosomal recessive"	Pepd (MGI:97542)			
chr19	33621954	33773508	19q13.1	19q13.11		610190	"CHST8, GALNAC4ST1, PSS3"	Carbohydrate sulfotransferase 8	CHST8	64377	ENSG00000124302	mutation has been identified in 1 PSS3 family	"?Peeling skin syndrome 3, 616265 (3), Autosomal recessive"	Chst8 (MGI:1916197)			
chr19	33795539	33815760	19q13.11	19q13.11		615240	KCTD15	Potassium channel tetramerization domain-containing protein 15	KCTD15	79047	ENSG00000153885			Kctd15 (MGI:2385276)			
chr19	34172446	34229514	19q13.11	19q13.11		610677	"LSM14A, RAP55"	LSM14A protein	LSM14A	26065	ENSG00000257103			Lsm14a (MGI:1914320)			
chr19	34353329	34402412	19q13.1	19q13.11		172400	GPI	Glucose phosphate isomerase; neuroleukin	GPI	2821	ENSG00000105220		"Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency, 613470 (3), Autosomal recessive"	Gpi1 (MGI:95797)			
chr19	34404397	34426167	19q13.11	19q13.11		615661	"PDCD2L, MGC13096"	Programmed cell death 2-like protein	PDCD2L	84306	ENSG00000126249			Pdcd2l (MGI:1915329)			
chr19	34428175	34469892	19q12	19q13.11		613295	"UBA2, SAE2"	Ubiquitin-like modifier-activating enzyme 2	UBA2	10054	ENSG00000126261			Uba2 (MGI:1858313)			
chr19	34481932	34509146	19q13.12	19q13.11		614790	WTIP	WT1-interacting protein	WTIP	126374	ENSG00000142279			Wtip (MGI:2141920)			
chr19	34590624	34594584	19q13.11	19q13.11		615063	SCGB2B2	"Secretoglobin, family 2B, member 2"	SCGB2B2	284402	ENSG00000205209						
chr19	34734193	34746482	19q13.2	19q13.11		606741	ZNF181	Zinc finger protein-181	ZNF181	339318	ENSG00000197841						
chr19	35030687	35040448	19q13.1	19q13.11		600235	"SCN1B, GEFSP1, BRGDA5, ATFB13, EIEE52"	"Sodium channel, voltage-gated, type I, beta polypeptide"	SCN1B	6324	ENSG00000105711		"Atrial fibrillation, familial, 13, 615377 (3), Autosomal dominant; Brugada syndrome 5, 612838 (3); Cardiac conduction defect, nonspecific, 612838 (3); Epilepsy, generalized, with febrile seizures plus, type 1, 604233 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 52, 617350 (3), Autosomal recessive"	Scn1b (MGI:98247)			
chr19	35040505	35066572	19q11-q13.2	19q13.11		142440	HPN	Hepsin	HPN	3249	ENSG00000105707			Hpn (MGI:1196620)			
chr19	35115817	35124323	19q13.12	19q13.12		604996	"FXYD3, PLML, MAT8"	FXYD domain-containing ion transport regulator 3	FXYD3	5349	ENSG00000089356			Fxyd3 (MGI:107497)			
chr19	35124512	35135273	19q13.11	19q13.12		608303	"LGI4, AMCNMY"	"Leucine-rich gene, glioma-inactivated, 4"	LGI4	163175	ENSG00000153902		"Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468 (3), Autosomal recessive"	Lgi4 (MGI:2180197)			
chr19	35137205	35143054	19q13.1	19q13.12		602359	"FXYD1, PLM"	FXYD domain-containing ion transport regulator 1 (phospholemman)	FXYD1	5348	ENSG00000266964			Fxyd1 (MGI:1889273)			
chr19	35143249	35154301	19q13.12	19q13.12		606684	FXYD7	FXYD domain-containing ion transport regulator 7	FXYD7	53822	ENSG00000221946			Fxyd7 (MGI:1889006)			
chr19	35154721	35169884	19q13.12	19q13.12		606669	FXYD5	FXYD domain-containing ion transport regulator 5	FXYD5	53827	ENSG00000089327			Fxyd5 (MGI:1201785)			
chr19	35248655	35267963	19q13.12	19q13.12		616582	LSR	Lipolysis-stimulated lipoprotein receptor	LSR	51599	ENSG00000105699			Lsr (MGI:1927471)			
chr19	35268977	35279820	19q13.1	19q13.12		600390	"USF2, FIP"	"Upstream transcription factor 2, c-fos interacting"	USF2	7392	ENSG00000105698			Usf2 (MGI:99961)			
chr19	35282345	35285142	19q13	19q13.12		606464	"HAMP, LEAP1, HEPC, HFE2B"	Hepcidin antimicrobial peptide	HAMP	57817	ENSG00000105697	digenic form with HAMP and HFE mutations	"Hemochromatosis, type 2B, 613313 (3), Autosomal recessive"				
chr19	35292085	35313806	19q13.1	19q13.12		159460	"MAG, GMA, SPG75"	Myelin-associated glycoprotein	MAG	4099	ENSG00000105695		"Spastic paraplegia 75, autosomal recessive, 616680 (3), Autosomal recessive"	Mag (MGI:96912)			
chr19	35329165	35347360	19q13.1	19q13.12		107266	CD22	CD22 antigen	CD22	933	ENSG00000012124			Cd22 (MGI:88322)			
chr19	35351541	35352463	19q13.1	19q13.12		603820	"FFAR1, GPR40"	Free fatty acid receptor 1	FFAR1	2864	ENSG00000126266			Ffar1 (MGI:2684079)			
chr19	35358105	35360490	19q13.1	19q13.12		603821	"FFAR3, GPR41"	Free fatty acid receptor 3	FFAR3	2865	ENSG00000185897			Ffar3 (MGI:2685324)			
chr19	35371094	35372452	19q13.1	19q13.12		603822	GPR42	G protein-coupled receptor-42	GPR42	2866	ENSG00000126251						
chr19	35447964	35451766	19q13.1	19q13.12		603823	"FFAR2, GPR43"	Free fatty acid receptor 2	FFAR2	2867	ENSG00000126262			Ffar2 (MGI:2441731)			
chr19	35487323	35490530	19q13.1	19q13.12		617212	KDAP	Keratinocyte differentiation-associated protein	KRTDAP	388533	ENSG00000188508			Krtdap (MGI:1928282)			
chr19	35497216	35513677	19q13.1	19q13.12		617211	DMKN	Dermokine	DMKN	93099	ENSG00000161249			Dmkn (MGI:1920962)			
chr19	35523366	35528370	19q13.1	19q13.12		609969	SBSN	Suprabasin	SBSN	374897	ENSG00000189001			Sbsn (MGI:2446326)			
chr19	35533411	35545318	19q13.1	19q13.12		609169	"GAPDHS, GAPD2"	"Glyceraldehyde-3-phosphate dehydrogenase, spermatogenic"	GAPDHS	26330	ENSG00000105679	9.5 Mbp prox. to APOE		Gapdhs (MGI:95653)			
chr19	35550192	35563657	19q13.1	19q13.12		137216	"ATP4A, ATP6A"	"ATPase, H+, K+ transporting, alpha"	ATP4A	495	ENSG00000105675			Atp4a (MGI:88113)			
chr19	35612743	35625348	19q13.12	19q13.12		613432	"HAUS5, DGT5, KIAA0841"	"HAUS augmin-like complex, subunit 5"	HAUS5	23354	ENSG00000249115			Haus5 (MGI:1919159)			
chr19	35629015	35637685	19q13.12	19q13.12		613232	RBM42	RNA-binding motif protein 42	RBM42	79171	ENSG00000126254			Rbm42 (MGI:1915285)			
chr19	35641174	35644870	19q13.1	19q13.12		609358	"ETV2, ETSRP71"	ETS variant gene 2	ETV2	2116	ENSG00000105672			Etv2 (MGI:99253)			
chr19	35648222	35658783	19q13.1	19q13.12		124089	COX6B1	"Cytochrome c oxidase, subunit VIb polypeptide 1 (ubiquitous)"	COX6B1	1340	ENSG00000126267		"Mitochondrial complex IV deficiency, 220110 (3), Autosomal recessive, Mitochondrial"	Cox6b1 (MGI:107460)			
chr19	35666515	35678484	19q13.1	19q13.12		611557	"UPK1A, UPIA"	Uroplakin 1A	UPK1A	11045	ENSG00000105668			Upk1a (MGI:98911)			
chr19	35704480	35717047	19q13.1	19q13.12		605859	"ZBTB32, FAXF, TZFP, ROG"	Zinc finger- and BTB domain-containing protein 32	ZBTB32	27033	ENSG00000011590			Zbtb32 (MGI:1891838)			
chr19	35717817	35738879	19q13.1	19q13.12		606834	"KMT2B, MLL4, KIAA0304, DYT28"	Lysine (K)-specific methyltransferase 2B	KMT2B	9757	ENSG00000272333		"Dystonia 28, childhood-onset, 617284 (3), Autosomal dominant"	Kmt2b (MGI:109565)			
chr19	35738800	35742449	19q13.12	19q13.12		614143	"IGFLR1, TMEM149"	IGF-like family receptor 1	IGFLR1	79713	ENSG00000126246			Igflr1 (MGI:3655979)			
chr19	35742526	35745441	19q13.2	19q13.12		601080	"U2AF1L4, U2AF1RS3"	U2 small nuclear RNA auxillary factor 1-like 4	U2AF1L4	199746	ENSG00000161265						
chr19	35745576	35747518	19q13.1	19q13.12		607632	"PSENEN, PEN2, ACNINV2"	"Presenilin enhancer 2, C. elegans, homolog of"	PSENEN	55851	ENSG00000205155		"Acne inversa, familial, 2, with or without Dowling-Degos disease, 613736 (3), Autosomal dominant"	Psenen (MGI:1913590)			
chr19	35754565	35757028	19q13.13	19q13.12		610695	"HSPB6, HSP20"	Heat-shock 27kD protein 6	HSPB6	126393	ENSG00000004776			Hspb6 (MGI:2685325)			
chr19	35775514	35788821	19q13.12	19q13.12		614902	"ARHGAP33, TCGAP"	Rho GTPase-activating protein 33	ARHGAP33	115703	ENSG00000004777			Arhgap33 (MGI:2673998)			
chr19	35799986	35813298	19q13.12	19q13.12		616377	"PRODH2, HYPDH"	Proline dehydrogenase (oxidase) 2	PRODH2	58510	ENSG00000250799			Prodh2 (MGI:1929093)			
chr19	35825371	35851992	19q13.1	19q13.12		602716	"NPHS1, NPHN"	Nephrin	NPHS1	4868	ENSG00000161270		"Nephrotic syndrome, type 1, 256300 (3), Autosomal recessive"	Nphs1 (MGI:1859637)			
chr19	35851634	35867145	19q13.1	19q13.12		607762	"KIRREL2, NEPH3, NLG1, FILTRIN"	Kin or IRRE-like 2 (nephrin-like 3)	KIRREL2	84063	ENSG00000126259			Kirrel2 (MGI:2442334)			
chr19	35868444	35879796	19q13.2	19q13.12		104775	"APLP1, APLP"	Amyloid beta (A4) precursor-like protein-1	APLP1	333	ENSG00000105290			Aplp1 (MGI:88046)			
chr19	35902364	35904270	19q13.1	19q13.12		604089	DAP10	DNAX-activation protein 10	HCST	10870	ENSG00000126264			Hcst (MGI:1344360)			
chr19	35904400	35908308	19q13.1	19q13.12		604142	"TYROBP, PLOSL, DAP12"	TYRO protein tyrosine kinase-binding protein	TYROBP	7305	ENSG00000011600		"Nasu-Hakola disease, 221770 (3), Autosomal recessive"	Tyrobp (MGI:1277211)			
chr19	35937119	35945194	19q13.2	19q13.12		612809	"LRFN3, SALM4"	Leucine-rich repeat and fibronectin type III domain-containing protein 3	LRFN3	79414	ENSG00000126243			Lrfn3 (MGI:2442512)			
chr19	35995187	35996317	19q12-q13.2	19q13.12		612848	SDHAF1	Succinate dehydrogenase complex assembly factor 1	SDHAF1	644096	ENSG00000205138		"Mitochondrial complex II deficiency, 252011 (3), Autosomal recessive"	Sdhaf1 (MGI:1915582)			
chr19	36003298	36008792	19q13.12	19q13.12		615535	"SYNE4, NESP4, C19orf46, DFNB76"	Spectrin repeat-containing nuclear envelope protein 4	SYNE4	163183	ENSG00000181392		"Deafness, autosomal recessive 76, 615540 (3), Autosomal recessive"	Syne4 (MGI:2141950)			
chr19	36009115	36014242	19q13.12	19q13.12		613304	"ALKBH6, ABH6"	"AlkB, E. coli, homolog of, 6"	ALKBH6	84964	ENSG00000239382			Alkbh6 (MGI:2142037)			
chr19	36014659	36032894	19q13	19q13.12		607382	"CLIP3, CLIPR59"	"CAP-GLY domain-containing linker protein 3, 607382 (3)"	CLIP3	25999	ENSG00000105270			Clip3 (MGI:1923936)			
chr19	36034984	36054761	19q13.12	19q13.12		612536	THAP8	THAP domain-containing protein 8	THAP8	199745	ENSG00000161277						
chr19	36054880	36111144	19q13.12	19q13.12		613583	"WDR62, C19orf14, MCPH2"	WD repeat-containing protein 62	WDR62	284403	ENSG00000075702		"Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, 604317 (3), Autosomal recessive"	Wdr62 (MGI:1923696)			
chr19	36111179	36113710	19q13.1	19q13.12		616442	OVOL3	ovo-like 3	OVOL3	728361	ENSG00000105261			Ovol3 (MGI:2388075)			
chr19	36113708	36115303	19q12	19q13.12		180662	POLR2I	"Polymerase (RNA) II (DNA directed) polypeptide I, 14.5kD"	POLR2I	5438	ENSG00000105258			Polr2i (MGI:1917170)			
chr19	36114948	36125947	19q13.11-q13.12	19q13.12		601303	CKAP1	Cytoskeleton-associated protein 1	TBCB	1155	ENSG00000105254			Tbcb (MGI:1913661)			
chr19	36139925	36150352	19q13.12	19q13.12		114170	"CAPNS1, CAPN4"	"Calpain, small polypeptide"	CAPNS1	826	ENSG00000126247			Capns1 (MGI:88266)			
chr19	36150921	36152868	19q13.12	19q13.12		123995	"COX7A1, COX7AM"	"Cytochrome c oxidase, subunit VIIa, polypeptide-1, muscle"	COX7A1	1346	ENSG00000161281			Cox7a1 (MGI:1316714)			
chr19	36182059	36215083	19q13.12	19q13.12		614275	ZNF565	Zinc finger protein 565	ZNF565	147929	ENSG00000196357			Zfp84 (MGI:107780)			
chr19	36214601	36238773	19q13.1	19q13.12		601505	"ZNF146, OZF"	Zinc finger protein-146	ZNF146	7705	ENSG00000167635			Zfp146 (MGI:1347092)			
chr19	36510686	36528487	19q13.12	19q13.12		613749	"ZNF260, PEX1"	Zinc finger protein 260	ZNF260	339324	ENSG00000254004			Zfp260 (MGI:1347071)			
chr19	36605304	36628596	19q13.13	19q13.12		609516	"ZNF382, KS1"	Zinc finger protein 382	ZNF382	84911	ENSG00000161298			Zfp382 (MGI:3588204)			
chr19	36636620	36666852	19q13.4	19q13.12		608640	"ZNF461, GIOT1"	Zinc finger protein-461	ZNF461	92283	ENSG00000197808						
chr19	36916328	36997931	19q13.12	19q13.12		617566	"ZNF568, ZFP568"	Zinc finger protein 568	ZNF568	374900	ENSG00000198453						
chr19	37007814	37130366	19q13.12	19q13.12		617216	"ZNF420, APAK"	Zinc finger protein 420	ZNF420	147923	ENSG00000197050			Zfp420 (MGI:2444666)			
chr19	37312836	37364454	19q13.12	19q13.12		165250	HKR1	GLI-Kruppel family member HKR1 (oncogene HKR1)	HKR1	284459	ENSG00000181666						
chr19	37411141	37469262	19q13.12	19q13.12		613904	ZNF569	Zinc finger protein 569	ZNF569	148266	ENSG00000196437			Zfp74 (MGI:107784)			
chr19	37551370	37614178	19q13.13	19q13.12		613903	ZNF540	Zinc finger protein 540	ZNF540	163255	ENSG00000171817						
chr19	37631008	37656260	19q13.12	19q13.12		617317	"ZFP30, ZNF745, KIAA0961"	"Zinc finger protein 30, mouse, homolog of"	ZFP30	22835	ENSG00000120784			Zfp30 (MGI:99178)			
chr19	37906821	38208371	19q13.1	19q13.1-q13.2		616655	"SIPA1L3, SPAL3, SPAR3, KIAA0545, CTRCT45"	SIPA1-like protein 3	SIPA1L3	23094	ENSG00000105738	mutation identified in 1 CTRCT45 family	"?Cataract 45, 616851 (3), Autosomal recessive"	Sipa1l3 (MGI:1921456)			
chr19	38200000	58617616	19q13.2-q13.4			603855	CFM1	Cystic fibrosis modifier-1	CFM1	10167			"{Meconium ileus in cystic fibrosis, susceptibility to}, 603855 (2)"				
chr19	38200000	50900000	19q13.2-q13.3			611097	MRT11	"Mental retardation, autosomal recessive, 11"	MRT11	100101426		between rs2109075 and rs8101149	"Mental retardation, autosomal recessive, 11, 611097 (2), Autosomal recessive"				
chr19	38200000	42900000	19q13.2			227050	TEC	Transient erythroblastopenia of childhood		100124696			"Transient erythroblastopenia of childhood, 227050 (2), Autosomal recessive"				
chr19	38200000	50900000	19q13.2-q13.3			165060	"TRNAU1, TRSP"	Transfer RNA selenocysteine 1 (anticodon UCA)	TRU-TCA1-1	7234		pseudogene on 22					
chr19	38211005	38229713	19q13.13-q13.2	19q13.2		601670	"DPF1, NEUD4"	"D4, zinc, and double PHD fingers family, member 1"	DPF1	8193	ENSG00000011332			Dpf1 (MGI:1352748)			
chr19	38251236	38256590	19q13.1	19q13.2		608153	"PPP1R14A, CPI17"	"Protein phosphatase 1, regulatory subunit 14A"	PPP1R14A	94274	ENSG00000167641			Ppp1r14a (MGI:1931139)			
chr19	38264457	38292613	19q13.1	19q13.2		605124	"SPINT2, HAI2, DIAR3"	"Serine protease inhibitor, Kunitz-type, 2 (hepatocyte growth factor activator inhibitor 2; bikunin, placental)"	SPINT2	10653	ENSG00000167642		"Diarrhea 3, secretory sodium, congenital, syndromic, 270420 (3), Autosomal recessive"	Spint2 (MGI:1338031)			
chr19	38319843	38329013	19q13.1	19q13.2		603939	"KCNK6, TWIK2, TOSS"	"Potassium channel, subfamily K, member 6"	KCNK6	9424	ENSG00000099337			Kcnk6 (MGI:1891291)			
chr19	38335562	38370948	19q13.1	19q13.2		613452	CATSPERG	"Cation channel, sperm-associated, gamma"	CATSPERG	57828	ENSG00000099338			"Catsperg2,Catsperg1 (MGI:2443617,MGI:1923968)"			
chr19	38374549	38383823	19q13.2	19q13.2		617844	PSMD8	"Proteasome 26S subunit, non-ATPase, 8"	PSMD8	5714	ENSG00000099341			Psmd8 (MGI:1888669)			
chr19	38384346	38388602	19q13.2	19q13.2		609966	GGN	"Gametogenetin, mouse, homolog of"	GGN	199720	ENSG00000179168			Ggn (MGI:2181461)			
chr19	38390060	38399883	19q13.13	19q13.2		609293	SPRED3	Sprouty-related EVH1 domain-containing protein 3	SPRED3	399473	ENSG00000188766			Spred3 (MGI:2142186)			
chr19	38409054	38426304	19q13.1	19q13.2		607320	RASGRP4	Ras guanyl nucleotide-releasing protein 4	RASGRP4	115727	ENSG00000171777			Rasgrp4 (MGI:2386851)			
chr19	38433699	38587563	19q13.1	19q13.2		180901	"RYR1, MHS, CCO"	"Ryanodine receptor-1, skeletal"	RYR1	6261	ENSG00000196218		"Central core disease, 117000 (3), Autosomal recessive, Autosomal dominant; King-Denborough syndrome, 145600 (3), Autosomal dominant; {Malignant hyperthermia susceptibility 1}, 145600 (3), Autosomal dominant; Minicore myopathy with external ophthalmoplegia, 255320 (3), Autosomal recessive; Neuromuscular disease, congenital, with uniform type 1 fiber, 117000 (3), Autosomal recessive, Autosomal dominant"	Ryr1 (MGI:99659)			
chr19	38587639	38618034	19q13.1-q13.4	19q13.2		601983	"MAP4K1, HPK1"	Mitogen-activated protein kinase kinase kinase kinase 1	MAP4K1	11184	ENSG00000104814			Map4k1 (MGI:1346882)			
chr19	38619071	38636958	19q13.2	19q13.2		609596	"EIF3K, PLAC24, EIF3S12"	"Eukaryotic translation initiation factor 3, subunit K"	EIF3K	27335	ENSG00000178982			Eif3k (MGI:1921080)			
chr19	38647615	38730531	19q13	19q13.2		604638	"ACTN4, FSGS1, FSGS"	"Actinin, alpha-4"	ACTN4	81	ENSG00000130402		"Glomerulosclerosis, focal segmental, 1, 603278 (3), Autosomal dominant"	Actn4 (MGI:1890773)			
chr19	38730047	38744473	19q13	19q13.2		608839	CAPN12	Calpain 12	CAPN12	147968	ENSG00000182472			Capn12 (MGI:1891369)			
chr19	38770967	38773516	19q13.2	19q13.2		600615	LGALS7	"Lectin, galactoside-binding, soluble, 7 (galectin 7)"	LGALS7	3963	ENSG00000205076			Lgals7 (MGI:1316742)			
chr19	38789209	38791753	19q13.2	19q13.2		617139	LGALS7B	"Lectin, galactoside-binding, soluble, 7B"	LGALS7B	653499	ENSG00000205076			Lgals7 (MGI:1316742)			
chr19	38801670	38813613	19q13.2	19q13.2		602518	LGALS4	"Lectin, galactoside-binding, soluble, 4"	LGALS4	3960	ENSG00000171747			Lgals4 (MGI:107536)			
chr19	38815421	38831856	19q13	19q13.2		600696	ECH1	"Enoyl Coenzyme A hydratase 1, peroxisomal"	ECH1	1891	ENSG00000104823			Ech1 (MGI:1858208)			
chr19	38836377	38852338	19q13.2	19q13.2		603083	"HNRNPL, HNRPL"	Heterogeneous nuclear riboprotein 1	HNRNPL	3191	ENSG00000104824			Hnrnpl (MGI:104816)			
chr19	38878554	38899861	19q	19q13.2		604480	"SIRT2, SIR2L, SIR2L2"	"Sirtuin, S. cerevisiae, homolog 2"	SIRT2	22933	ENSG00000068903			Sirt2 (MGI:1927664)			
chr19	38899502	38908893	19q13.1	19q13.2		604495	"NFKBIB, IKBB, TRIP9"	"Nuclear factor of kappa light chain gene enhancer in B cells inhibitor, beta"	NFKBIB	4793	ENSG00000104825			Nfkbib (MGI:104752)			
chr19	38908170	38914370	19q13.2	19q13.2		617634	CCER2	Coiled-coil glutamate-rich protein 2	CCER2	643669	ENSG00000262484			Ccer2 (MGI:3645242)			
chr19	38915263	38930895	19q13.2	19q13.2		612804	SARS2	Seryl-tRNA synthetase 2	SARS2	54938	ENSG00000104835		"Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis, 613845 (3), Autosomal recessive"	Sars2 (MGI:1919234)			
chr19	38930707	38933019	19q13.1	19q13.2		603021	"MRPS12, RPSM12"	"Ribosomal protein, mitochondrial, S12"	MRPS12	6183	ENSG00000128626			Mrps12 (MGI:1346333)			
chr19	38941400	38975812	19q13.2	19q13.2		609094	"FBXO17, FBX17, FBX26, FBG4"	F-box only protein 17	FBXO17	115290	ENSG00000269190			Fbxo17 (MGI:1354707)			
chr19	39007063	39032595	19q13.2	19q13.2		609099	"FBXO27, FBX27, FBG5"	F-box only protein 27	FBXO27	126433	ENSG00000161243			Fbxo27 (MGI:2685007)			
chr19	39083010	39112073	19q13.2	19q13.2		610490	"PAPL, FLJ16165"	"Purple acid phosphatase, long form"	ACP7	390928	ENSG00000183760			Acp7 (MGI:2142121)			
chr19	39125779	39179405	19q13.2	19q13.2		605451	PAK4	p21-activated kinase 4	PAK4	10298	ENSG00000130669			Pak4 (MGI:1917834)			
chr19	39196963	39201881	19q13.2	19q13.2		615901	"NCCRP1, FBXO50"	"Nonspecific cytotoxic cell receptor protein 1, zebrafish, homolog of"	NCCRP1	342897	ENSG00000188505			Nccrp1 (MGI:2685009)			
chr19	39243605	39245076	19q13.13	19q13.2		607402	"IFNL3, IL28B"	"Interferon, lambda 3"	IFNL3	282617	ENSG00000197110		"{Hepatitis C virus infection, response to therapy of}, 609532 (3)"	"Ifnl2,Ifnl3 (MGI:3647279,MGI:2450574)"			
chr19	39246313	39248855	19q13.13	19q13.2		615090	IFNL4	"Interferon, lambda-4"	IFNL4	101180976	ENSG00000272395						
chr19	39268516	39270091	19q13.13	19q13.2		607401	"IFNL2, IL28A"	"Interferon, lambda 2"	IFNL2	282616	ENSG00000183709						
chr19	39296324	39298671	19q13.13	19q13.2		607403	"IFNL1, IL29"	"Interferon, lambda 1"	IFNL1	282618	ENSG00000182393						
chr19	39306816	39320866	19q13.2	19q13.2		612807	"LRFN1, SALM2, KIAA1484"	Leucine-rich repeat and fibronectin type III domain-containing protein 1	LRFN1	57622	ENSG00000128011			Lrfn1 (MGI:2136810)			
chr19	39328356	39336085	19q13.2	19q13.2		604104	GMFG	"Glia maturation factor, gamma"	GMFG	9535	ENSG00000130755			"Gmfg,Gmfg-ps (MGI:1927135,MGI:3704264)"			
chr19	39385628	39391194	19q13.2	19q13.2		610506	"PAF1, PD2"	"PAF1 RNA polymerase II-associated factor, S. cerevisiae, homolog of"	PAF1	54623	ENSG00000006712			Paf1 (MGI:1923988)			
chr19	39391302	39400636	19q13.2	19q13.2		612914	"MED29, IXL"	Mediator complex subunit 29	MED29	55588	ENSG00000063322			Med29 (MGI:1914474)			
chr19	39406846	39409411	19q13.1	19q13.2		190700	"ZFP36, TTP"	"Zfp36, mouse, homolog of"	ZFP36	7538	ENSG00000128016			Zfp36 (MGI:99180)			
chr19	39412581	39428414	19q13.1	19q13.2		611893	"PLEKHG2, CLG, LDAMD"	"Pleckstrin homology domain-containing protein, family G, member 2"	PLEKHG2	64857	ENSG00000090924		"Leukodystrophy and acquired microcephaly with or without dystonia, 616763 (3), Autosomal recessive"	Plekhg2 (MGI:2141874)			
chr19	39433136	39436019	19q	19q13.2		603675	RPS16	Ribosomal protein S16	RPS16	6217	ENSG00000105193			Rps16 (MGI:98118)			
chr19	39445545	39476669	19q13.1-q13.2	19q13.2		602102	"SUPT5H, SPT5"	"Suppressor of Ty 5, S. cerevisiae, homolog of"	SUPT5H	6829	ENSG00000196235			Supt5 (MGI:1202400)			
chr19	39480411	39493784	19q13.2	19q13.2		607381	"TIMM50, TIM50, MGCA9"	"Translocase of inner mitochondrial membrane 50, yeast, homolog of"	TIMM50	92609	ENSG00000105197		"3-methylglutaconic aciduria, type IX, 617698 (3), Autosomal recessive"	Timm50 (MGI:1913775)			
chr19	39498916	39508480	19q13	19q13.2		602768	"DLL3, SCDO1"	"Delta, Drosophila, homolog of"	DLL3	10683	ENSG00000090932		"Spondylocostal dysostosis 1, autosomal recessive, 277300 (3), Autosomal recessive"	Dll3 (MGI:1096877)			
chr19	39515112	39520685	19q13.13	19q13.2		607919	"SELENOV, SELV"	Selenoprotein V	SELENOV	348303	ENSG00000186838			Selenov (MGI:3608324)			
chr19	39538805	39540197	19q13.2	19q13.2		609773	"EID2, CRI2"	EP300-interacting inhibitor of differentiation 2	EID2	163126	ENSG00000176396			Eid2 (MGI:2681174)			
chr19	39602410	39607473	19q13.1	19q13.2		608717	"LGALS13, GAL13, PP13"	"Lectin, galactoside-binding, soluble, 13"	LGALS13	29124	ENSG00000105198						
chr19	39704305	39709447	19q13.2	19q13.2		607260	PPL13	Placental protein 13-like protein	LGALS14	56891	ENSG00000006659						
chr19	39731252	39738028	19q13.1	19q13.2		153310	CLC	Charcot-Leyden crystal protein	CLC	1178	ENSG00000105205						
chr19	39825346	39834232	19q12-q13.11	19q13.2		604556	"DYRK1B, MIRK, AOMS3"	Dual-specificity tyrosine phosphorylation-regulated kinase 1B	DYRK1B	9149	ENSG00000105204		"Abdominal obesity-metabolic syndrome 3, 615812 (3), Autosomal dominant"	Dyrk1b (MGI:1330302)			
chr19	39834452	39846413	19q13.2	19q13.2		134795	FBL	Fibrillarin	FBL	2091	ENSG00000105202			Fbl (MGI:95486)			
chr19	39863322	39934625	19q13.2	19q13.2		617553	FCGBP	Fc fragment of IgG-binding protein	FCGBP	8857	ENSG00000275395			Fcgbp (MGI:2444336)			
chr19	39971004	39981763	19q13.11-q13.13	19q13.2		602707	"PSMC4, TBP7, S6"	"Proteasome 26S subunit, ATPase, 4"	PSMC4	5704	ENSG00000013275			Psmc4 (MGI:1346093)			
chr19	40191656	40215574	19q13.1-q13.2	19q13.2		600137	"MAP3K10, MLK2, MST"	Mitogen-activated protein kinase kinase kinase 10	MAP3K10	4294	ENSG00000130758			Map3k10 (MGI:1346879)			
chr19	40230316	40285530	19q13.1-q13.2	19q13.2		164731	"AKT2, HIHGHH"	Murine thymoma viral (v-akt) homolog-2	AKT2	208	ENSG00000105221		"Diabetes mellitus, type II, 125853 (3), Autosomal dominant; Hypoinsulinemic hypoglycemia with hemihypertrophy, 240900 (3), Autosomal dominant"	Akt2 (MGI:104874)			
chr19	40348394	40378489	19q13.2	19q13.2		615698	"PLD3, HUK4, SCA46"	"Phospholipase D family, member 3"	PLD3	23646	ENSG00000105223	mutation identified in 1 SCA46 family	"?Spinocerebellar ataxia 46, 617770 (3), Autosomal dominant"	Pld3 (MGI:1333782)			
chr19	40379270	40390864	19q13.2	19q13.2		611712	HIPK4	Homeodomain-interacting protein kinase 4	HIPK4	147746	ENSG00000160396			Hipk4 (MGI:2685008)			
chr19	40393761	40414717	19q13.1-q13.2	19q13.2		605725	"PRX, CMT4F"	Periaxin	PRX	57716	ENSG00000105227		"Charcot-Marie-Tooth disease, type 4F, 614895 (3), Autosomal recessive; Dejerine-Sottas disease, 145900 (3), Autosomal recessive, Autosomal dominant"	Prx (MGI:108176)			
chr19	40422500	40426024	19q13.2	19q13.2		617850	"SERTAD1, TRIPBR1"	SERTA domain-containing protein 1	SERTAD1	29950	ENSG00000197019			Sertad1 (MGI:1913438)			
chr19	40440840	40444374	19q13.1	19q13.2		612125	"SERTAD3, RBT1"	SERTA domain-containing 3	SERTAD3	29946	ENSG00000167565			Sertad3 (MGI:2180697)			
chr19	40447783	40465817	19q13.13-q13.2	19q13.2		600941	"BLVRB, BVRB, FLR"	Biliverdin reductase B	BLVRB	645	ENSG00000090013			Blvrb (MGI:2385271)			
chr19	40467152	40576458	19q13.13	19q13.2		606214	"SPTBN4, QV, CMND"	"Spectrin, beta, nonerythrocytic, 4 (quivering, mouse, homolog of)"	SPTBN4	57731	ENSG00000160460	mutation identified in 1 CMND patient	"?Myopathy, congenital, with neuropathy and deafness, 617519 (3), Autosomal recessive"	Sptbn4 (MGI:1890574)			
chr19	40576850	40591398	19q13.2	19q13.2		617322	"SHKBP1, SB1"	SH3KBP1-binding protein 1	SHKBP1	92799	ENSG00000160410			Shkbp1 (MGI:2385803)			
chr19	40592887	40629819	19q13.1-q13.2	19q13.2		604710	"LTBP4, LTBP4S, LTBP4L, ARCL1C"	Latent transforming growth factor-beta-binding protein 4	LTBP4	8425	ENSG00000090006		"Cutis laxa, autosomal recessive, type IC, 613177 (3), Autosomal recessive"	Ltbp4 (MGI:1321395)			
chr19	40665904	40690657	19q13.13-q13.2	19q13.2		604018	"NUMBL, NUMBR, NBL"	"Numb, Drosophila, homolog-like"	NUMBL	9253	ENSG00000105245			Numbl (MGI:894702)			
chr19	40691528	40716884	19q13.1	19q13.2		615567	"COQ8B, ADCK4, NPHS9"	Coenzyme Q8B	COQ8B	79934	ENSG00000123815		"Nephrotic syndrome, type 9, 615573 (3), Autosomal recessive"	Coq8b (MGI:1924139)			
chr19	40717102	40740859	19q13.2	19q13.2		606476	ITPKC	"Inositol 1,4,5-trisphosphate 3-kinase C"	ITPKC	80271	ENSG00000086544		"{Kawasaki disease, susceptibility to}, 611775 (3)"	Itpkc (MGI:2442554)			
chr19	40750853	40765391	19q13.1	19q13.2		182285	SNRPA	Small nuclear ribonucleoprotein polypeptide A	SNRPA	6626	ENSG00000077312						
chr19	40775176	40777492	19q13.32-q13.33	19q13.2		601340	MIA	Melanoma inhibitory activity	MIA	8190	ENSG00000261857			Mia (MGI:109615)			
chr19	40778218	40796943	19q13.2-q13.3	19q13.2		612945	RAB4B	Ras-associated protein RAB4B	RAB4B	53916	ENSG00000167578			Rab4b (MGI:105071)			
chr19	40799142	40808440	19q13.2	19q13.2		606424	"EGLN2, PHD1, HIFPH1"	"Egl9, C. elegans, homolog of, 2"	EGLN2	112398	ENSG00000269858			Egln2 (MGI:1932287)			
chr19	40843537	40850446	19q13.2	19q13.2		122720	"CYP2A6, CYP2A3, CYP2A, P450C2A"	"Cytochrome P450, subfamily IIA, phenobarbital-inducible, polypeptide 6"	CYP2A6	1548	ENSG00000255974		"Coumarin resistance, 122700 (3), Autosomal dominant; {Lung cancer, resistance to}, 211980 (3), Autosomal recessive; {Nicotine addiction, protection from}, 188890 (3)"	"Cyp2a4,Cyp2a5 (MGI:88597,MGI:88596)"			
chr19	40875438	40885950	19q13.2	19q13.2		608054	CYP2A7	"Cytochrome P450, subfamily IIA, polypeptide 7"	CYP2A7	1549	ENSG00000198077			"Cyp2a4,Cyp2a5 (MGI:88597,MGI:88596)"			
chr19	40890825	40900507	19q13.2	19q13.2		601133	CYP2G1	"Cytochrome P450, subfamily IIG, polypeptide 1"	CYP2G1P	22952							
chr19	40991298	41018395	19q13.2	19q13.2		123930	"CYP2B6, CYP2B, EFVM"	"Cytochrome P450, family 2, subfamily B, polypeptide 6"	CYP2B6	1555	ENSG00000197408	same NotI fragment as CYP2A	"{Efavirenz central nervous system toxicity, susceptibility to}, 614546 (3); Efavirenz, poor metabolism of, 614546 (3)"	Cyp2b10 (MGI:88598)			
chr19	41088450	41096194	19q13.2	19q13.2		608055	CYP2A13	"Cytochrome P450, subfamily IIA, polypeptide 13"	CYP2A13	1553	ENSG00000197838			"Cyp2a4,Cyp2a5 (MGI:88597,MGI:88596)"			
chr19	41114291	41128380	19q13.2	19q13.2		124070	CYP2F1	"Cytochrome P450, subfamily IIF, polypeptide 1"	CYP2F1	1572	ENSG00000197446	"CYP2A, CYP2B, CYP2F1 in 240kb"		Cyp2f2 (MGI:88608)			
chr19	41193206	41207538	19q13.2	19q13.2		611529	CYP2S1	"Cytochrome P450, family 2, subfamily S, polypeptide 1"	CYP2S1	29785	ENSG00000167600			Cyp2s1 (MGI:1921384)			
chr19	41219198	41261766	19q13.1-q13.2	19q13.2		109135	AXL	AXL transforming sequence (a receptor tyrosine kinase)	AXL	558	ENSG00000167601			Axl (MGI:1347244)			
chr19	41262475	41307782	19q13.2	19q13.2		605800	"HNRNPUL1, HNRPUL1, E1BAP5"	Heterogeneous nuclear ribonucleoprotein U-like 1	HNRNPUL1	11100	ENSG00000105323			Hnrnpul1 (MGI:2443517)			
chr19	41330322	41353882	19q13.1	19q13.2		190180	"TGFB1, DPD1, CED"	"Transforming growth factor, beta-1"	TGFB1	7040	ENSG00000105329		"Camurati-Engelmann disease, 131300 (3), Autosomal dominant; {Cystic fibrosis lung disease, modifier of}, 219700 (3), Autosomal recessive"	Tgfb1 (MGI:98725)			
chr19	41354416	41364533	19q13.2	19q13.2		611951	"B9D2, MKS10, JBTS34"	B9 domain-containing protein 2	B9D2	80776	ENSG00000123810	mutation identified in 1 MKS10 family	"Joubert syndrome 34, 614175 (3), Autosomal recessive; ?Meckel syndrome 10, 614175 (3), Autosomal recessive"	B9d2 (MGI:2387643)			
chr19	41386369	41397350	19q13.2	19q13.2		606492	"EXOSC5, RRP46"	Exosome component 5	EXOSC5	56915	ENSG00000077348			Exosc5 (MGI:107889)			
chr19	41397788	41425004	19q13.1-q13.2	19q13.2		608348	"BCKDHA, MSUD1"	"Branched chain keto acid dehydrogenase E1, alpha polypeptide"	BCKDHA	593	ENSG00000248098		"Maple syrup urine disease, type Ia, 248600 (3), Autosomal recessive"	Bckdha (MGI:107701)			
chr19	41425358	41429023	19q13.2	19q13.2		615357	"B3GNT8, BGALT15, B3GALT7"	"Beta-1,3-galactosyltransferase 8"	B3GNT8	374907	ENSG00000177191			B3gnt8 (MGI:2385269)			
chr19	41431317	41447821	19q13.2	19q13.2		617262	ATP5SL	ATP5S-like protein	DMAC2	55101	ENSG00000105341			Dmac2 (MGI:1913599)			
chr19	41708584	41730432	19q13.2	19q13.2		114890	"CEACAM5, CEA"	Carcinoembryonic antigen-related cell adhesion molecule 5	CEACAM5	1048	ENSG00000105388	proximal to PSG cluster in 1.1-1.2Mb segment					
chr19	41755519	41772210	19q13.2	19q13.2		163980	"CEACAM6, NCA"	Carcinoembryonic antigen-related cell adhesion molecule 6 (non-specific crossreacting antigen)	CEACAM6	4680	ENSG00000086548	in CEA cluster					
chr19	41844742	41852329	19q13.2	19q13.2		614806	DMRTC2	Doublesex- and MAB3-related transcription factor C2	DMRTC2	63946	ENSG00000142025			Dmrtc2 (MGI:1918491)			
chr19	41859917	41871415	19q13.2	19q13.2		603474	"RPS19, DBA, DBA1"	Ribosomal protein S19	RPS19	6223	ENSG00000105372		"Diamond-Blackfan anemia 1, 105650 (3), Autosomal dominant"	Rps19 (MGI:1333780)			
chr19	41877119	41881371	19q13.2	19q13.2		112205	"CD79A, IGA"	CD79A antigen (immunoglobulin-associated alpha)	CD79A	973	ENSG00000105369		"Agammaglobulinemia 3, 613501 (3), Autosomal recessive"	Cd79a (MGI:101774)			
chr19	41883199	41907451	19q13.13	19q13.2		601855	"ARHGEF1, LBCL2"	"Rho guanine nucleotide exchange factor, 115-kD"	ARHGEF1	9138	ENSG00000076928			Arhgef1 (MGI:1353510)			
chr19	41956680	41959375	19q13.2	19q13.2		604925	PRA1	Prenylated RAB acceptor 1	RABAC1	10567	ENSG00000105404			Rabac1 (MGI:1201692)			
chr19	41966581	41994275	19q12-q13.2	19q13.2		182350	"ATP1A3, DYT12, RDP, AHC2, CAPOS"	"ATPase, Na+K+ transporting, alpha-3 polypeptide"	ATP1A3	478	ENSG00000105409		"Alternating hemiplegia of childhood 2, 614820 (3), Autosomal dominant; CAPOS syndrome, 601338 (3), Autosomal dominant; Dystonia-12, 128235 (3), Autosomal dominant"	Atp1a3 (MGI:88107)			
chr19	41998315	42071803	19q13.2	19q13.2		600283	GRIK5	"Glutamate receptor, ionotropic, kainate 5"	GRIK5	2901	ENSG00000105737			Grik5 (MGI:95818)			
chr19	42086109	42197930	19q13.2	19q13.2		164176	"POU2F2, OTF2, OCT2"	"POU domain, class 2, transcription factor 2"	POU2F2	5452	ENSG00000028277			Pou2f2 (MGI:101897)			
chr19	42198592	42220151	19q13.2	19q13.2		617078	"DEDD2, FLAME3"	Death effector domain-containing protein 2	DEDD2	162989	ENSG00000160570			Dedd2 (MGI:1914629)			
chr19	42220270	42227052	19q13.2	19q13.2		614387	"ZNF526, KIAA1951"	Zinc finger protein 526	ZNF526	116115	ENSG00000167625			Zfp526 (MGI:2445181)			
chr19	42247560	42255163	19q13.1	19q13.2		611888	"ERF, PE2, CRS4, CHYTS"	ETS2 repressor factor	ERF	2077	ENSG00000105722		"Chitayat syndrome, 617180 (3), Autosomal dominant; Craniosynostosis 4, 600775 (3), Autosomal dominant"	Erf (MGI:109637)			
chr19	42268536	42295795	19q13.2	19q13.2		612082	"CIC, KIAA0306, MRD45"	"Capicua, Drosophila, homolog of"	CIC	23152	ENSG00000079432		"Mental retardation, autosomal dominant 45, 617600 (3), Autosomal dominant"	Cic (MGI:1918972)			
chr19	42297032	42302799	19q13.1	19q13.2		603074	PAFAH1B3	"Platelet-activating factor acetylhydrolase, isoform Ib, gamma subunit"	PAFAH1B3	5050	ENSG00000079462			Pafah1b3 (MGI:108414)			
chr19	42325608	42378768	19q12	19q13.2		604267	"MEGF8, EGFL4, CRPT2"	Multiple epidermal growth factor-like domains 8	MEGF8	1954	ENSG00000105429		"Carpenter syndrome 2, 614976 (3), Autosomal recessive"	Megf8 (MGI:2446294)			
chr19	42387018	42390317	19q13	19q13.2		611764	CNFN	Cornifelin	CNFN	84518	ENSG00000105427			Cnfn (MGI:1919633)			
chr19	42401506	42427425	19q13.1-q13.2	19q13.2		151750	"LIPE, LHS, FPLD6"	"Lipase E, hormone-sensitive"	LIPE	3991	ENSG00000079435		"Lipodystrophy, familial partial, type 6, 615980 (3), Autosomal recessive"	Lipe (MGI:96790)			
chr19	42428537	42443047	19q11	19q13.2		611387	"CXCL17, VCC1, DMC"	Chemokine (C-X-C motif) ligand 17	CXCL17	284340	ENSG00000189377			Cxcl17 (MGI:2387642)			
chr19	42507305	42528508	19q13.2	19q13.2		109770	"CEACAM1, BGP"	Carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein)	CEACAM1	634	ENSG00000079385	in CEA cluster		"Ceacam1,Ceacam2 (MGI:1347246,MGI:1347245)"			
chr19	42580242	42595156	19q13.2	19q13.2		615747	"CEACAM8, CD66B, CGM6"	Carcinoembryonic antigen-related cell adhesion molecule 8	CEACAM8	1088	ENSG00000124469						
chr19	42721641	42740515	19q13.2	19q13.2		176392	PSG3	Pregnancy-specific beta-1-glycoprotein-3	PSG3	5671	ENSG00000221826						
chr19	42752686	42765691	19q13.2	19q13.2		176397	PSG8	Pregnancy-specific beta-1-glycoprotein-8	PSG8	440533	ENSG00000124467						
chr19	42836996	42855717	19q13.2	19q13.2		176399	"PSG10, PSG12"	Pregnancy-specific beta-1-glycoprotein-10	PSG10P	653492							
chr19	42866460	42879821	19q13.2	19q13.2		176390	"PSG1, PSBG1, B1G1, SP1"	Pregnancy-specific beta-1-glycoprotein-1	PSG1	5669	ENSG00000231924	distal to CEA					
chr19	42902081	42917923	19q13.2	19q13.31		176395	PSG6	Pregnancy-specific beta-1-glycoprotein-6	PSG6	5675	ENSG00000170848						
chr19	42924131	42937177	19q13.2	19q13.31		176396	PSG7	Pregnancy-specific beta-1-glycoprotein-7	PSG7	5676	ENSG00000221878						
chr19	43007656	43026478	19q13.2	19q13.31		176401	"PSG11, PSG13, PSG14"	Pregnancy-specific beta-1-glycoprotein-11	PSG11	5680	ENSG00000243130						
chr19	43064209	43082740	19q13.2	19q13.31		176391	"PSG2, PSBG2"	Pregnancy-specific beta-1-glycoprotein-2	PSG2	5670	ENSG00000242221						
chr19	43167742	43186535	19q13.2	19q13.31		176394	PSG5	Pregnancy-specific beta-1-glycoprotein-5	PSG5	5673	ENSG00000204941						
chr19	43192701	43205773	19q13.2	19q13.31		176393	PSG4	Pregnancy-specific beta-1-glycoprotein-4	PSG4	5672	ENSG00000243137						
chr19	43253281	43269562	19q13.2	19q13.31		176398	"PSG9, PSG11"	Pregnancy-specific beta-1-glycoprotein-9	PSG9	5678	ENSG00000183668						
chr19	43349055	43349547	19q13.2	19q13.31		605157	PRG1	p53-responsive gene 1		23574							
chr19	43353658	43366062	19q13.2	19q13.31		162860	"NB1, PRV1, CD177, HNA2A"	Neutrophil-specific antigen 1	CD177	57126	ENSG00000204936			Cd177 (MGI:1916141)			
chr19	43388610	43418614	19q13.31	19q13.31		612665	"TEX101, SGRG, TES101RP"	Testis-expressed gene 101	TEX101	83639	ENSG00000131126			Tex101 (MGI:1930791)			
chr19	43460793	43465678	19q13.1-q13.2	19q13.31		609484	LYPD3	LY6/PLAUR domain-containing protein 3	LYPD3	27076	ENSG00000124466			Lypd3 (MGI:1919684)			
chr19	43506718	43527255	19q13.32	19q13.31		608451	"ETHE1, HSCO, D83198"	ETHE1 gene	ETHE1	23474	ENSG00000105755		"Ethylmalonic encephalopathy, 602473 (3), Autosomal recessive"	Ethe1 (MGI:1913321)			
chr19	43543311	43575577	19q13.2	19q13.31		194360	"XRCC1, SCAR26"	"X-ray-repair, complementing defective, repair in Chinese hamster cells-1"	XRCC1	7515	ENSG00000073050	mutation identified in 1 SCAR26 patient	"?Spinocerebellar ataxia, autosomal recessive 26, 617633 (3), Autosomal recessive"	Xrcc1 (MGI:99137)			
chr19	43622367	43641983	19q13.2	19q13.31		609744	"CADM4, IGSF4C, TSLL2, NECL4, SYNCAM4"	Cell adhesion molecule 4	CADM4	199731	ENSG00000105767			Cadm4 (MGI:2449088)			
chr19	43646094	43670345	19q13	19q13.31		173391	"PLAUR, URKR"	"Plasminogen activator, urokinase, receptor"	PLAUR	5329	ENSG00000011422			Plaur (MGI:97612)			
chr19	43727991	43755035	19q13.31	19q13.31		613176	"C19orf61, SMG9, HBMS"	Chromosome 19 open reading frame 61	SMG9	56006	ENSG00000105771		"Heart and brain malformation syndrome, 616920 (3), Autosomal recessive"	Smg9 (MGI:1919247)			
chr19	43766532	43782138	19q13.2	19q13.31		602754	"KCNN4, KCA4, SK4, DHS2"	"Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4"	KCNN4	3783	ENSG00000104783		"Dehydrated hereditary stomatocytosis 2, 616689 (3), Autosomal dominant"	Kcnn4 (MGI:1277957)			
chr19	43912623	43935314	19q13.2	19q13.31		194554	"ZNF45, ZNF13, KOX5"	Zinc finger protein-45	ZNF45	7596	ENSG00000124459						
chr19	43967005	43998325	19q13.2-q13.32	19q13.31		604086	ZNF155	Zinc finger protein-155	ZNF155	7711	ENSG00000204920						
chr19	44025323	44033109	19q13.2	19q13.31		617357	ZNF222	Zinc finger protein 222	ZNF222	7673	ENSG00000159885						
chr19	44094328	44109830	19q13.2-qter	19q13.31		194555	"ZNF224, ZNF255, BMZF2, KOX22, ZNF27"	Zinc finger protein-224	ZNF224	7767	ENSG00000267680						
chr19	44141529	44160308	19q13.31	19q13.31		604750	"ZNF234, ZNF269, HZF4"	Zinc finger protein 234	ZNF234	10780	ENSG00000263002						
chr19	44286347	44305706	19q13.2	19q13.31		604749	"ZFP93, ANF270, HZF6"	"Zinc finger protein 93, mouse, homolog of"	ZNF235	9310	ENSG00000159917			Zfp235 (MGI:1929117)			
chr19	44326552	44367214	19p13.1-p12	19q13.31		603994	ZNF112	Zinc finger protein-112	ZNF112	7771	ENSG00000062370			Zfp112 (MGI:1929115)			
chr19	44474427	44500538	19q13.2	19q13.31		606740	ZNF180	Zinc finger protein-180	ZNF180	7733	ENSG00000167384			Zfp180 (MGI:1923701)			
chr19	44643797	44666160	19q13.2-q13.3	19q13.31		173850	"PVR, PVS"	Polio virus receptor	PVR	5817	ENSG00000073008						
chr19	44699150	44710713	19q13.31	19q13.31-q13.32		614591	"CEACAM16, CEAL2, DFNA4B"	Carcinoembryonic antigen-related cell adhesion molecule 16	CEACAM16	388551	ENSG00000213892		"Deafness, autosomal dominant 4B, 614614 (3), Autosomal dominant"	Ceacam16 (MGI:2685615)			
chr19	44742619	44760043	19q13	19q13.32		109560	BCL3	B-cell CLL/lymphoma-3	BCL3	602	ENSG00000069399		"Leukemia/lymphoma, B-cell, 3, 109560 (2)"	Bcl3 (MGI:88140)			
chr19	44777854	44800645	19q13.2	19q13.32		608453	CBLC	CAS-BR-M murine ecotropic retroviral transforming sequence C	CBLC	23624	ENSG00000142273			Cblc (MGI:1931457)			
chr19	44809058	44821420	19q13.2	19q13.32		612773	"LU, AU, BCAM"	B-cell adhesion molecule	BCAM	4059	ENSG00000187244	linked to SE	"[Blood group, Auberger system], 111200 (3); [Blood group, Lutheran null], 247420 (3), Autosomal recessive; [Blood group, Lutheran system], 111200 (3)"	Bcam (MGI:1929940)			
chr19	44846135	44889227	19q13.2	19q13.32		600798	"NECTIN2, PVRL2, HVEB, PVRR2, PRR2"	Nectin 2	NECTIN2	5819	ENSG00000130202			Nectin2 (MGI:97822)			
chr19	44891219	44903688	19q13.2	19q13.32		608061	"TOMM40, TOM40, PEREC1"	"Translocase of outer mitochondrial membrane 40, yeast, homolog of"	TOMM40	10452	ENSG00000130204			Tomm40 (MGI:1858259)			
chr19	44905748	44909394	19q13.2	19q13.32		107741	"APOE, AD2, LPG, LDLCQ5"	Apolipoprotein E	APOE	348	ENSG00000130203	possible 2nd locus for AD2 on chr.19	"Alzheimer disease-2, 104310 (3), Autosomal dominant; {Coronary artery disease, severe, susceptibility to}, 617347 (3); Hyperlipoproteinemia, type III, 617347 (3); Lipoprotein glomerulopathy, 611771 (3); {?Macular degeneration, age-related}, 603075 (3), Autosomal dominant; Sea-blue histiocyte disease, 269600 (3), Autosomal recessive"	Apoe (MGI:88057)			
chr19	44914246	44919348	19q13.2	19q13.32		107710	APOC1	Apolipoprotein C-I	APOC1	341	ENSG00000130208						
chr19	44942237	44945495	19q13.2	19q13.32		600745	APOC4	Apolipoprotein C-IV	APOC4	346	ENSG00000267467	555bp upstream of APOC2		Apoc4 (MGI:87878)			
chr19	44945981	44949564	19q13.2	19q13.32		608083	APOC2	Apolipoprotein C-II	APOC2	344	ENSG00000234906		"Hyperlipoproteinemia, type Ib, 207750 (3), Autosomal recessive"	Apoc2 (MGI:88054)			
chr19	44954584	44993345	19q13.3	19q13.32		604783	CLPTM1	Cleft lip and palate-associated transmembrane protein 1	CLPTM1	1209	ENSG00000104853			Clptm1 (MGI:1927155)			
chr19	45001448	45038197	19q13.32	19q13.32		604758	"RELB, IREL, IMD53"	v-rel avian reticuloendotheliosis viral oncogene homolog B	RELB	5971	ENSG00000104856	mutation identified in 1 IMD53 family	"?Immunodeficiency 53, 617585 (3), Autosomal recessive"	Relb (MGI:103289)			
chr19	45071499	45076587	19q13.32	19q13.32		613226	"ZNF296, ZFP296, ZNF342"	Zinc finger protein 296	ZNF296	162979	ENSG00000170684			Zfp296 (MGI:1926956)			
chr19	45075716	45091523	19q13.32	19q13.32		607419	GEMIN7	GEM-associated protein 7	GEMIN7	79760	ENSG00000142252			Gemin7 (MGI:1916981)			
chr19	45162927	45179265	19q13.32	19q13.32		610396	TRAPPC6A	"Trafficking protein particle complex, subunit 6A"	TRAPPC6A	79090	ENSG00000007255			Trappc6a (MGI:1914341)			
chr19	45178744	45202714	19q13	19q13.32		609762	"BLOC1S3, BLOS3, HPS8"	"Biogenesis of lysosome-related organelles complex 1, subunit 3"	BLOC1S3	388552	ENSG00000189114		"Hermansky-Pudlak syndrome 8, 614077 (3), Autosomal recessive"	Bloc1s3 (MGI:2678952)			
chr19	45212376	45234210	19q13.32	19q13.32		616927	"EXOC3L2, XTP7"	Exocyst complex component 3-like 2	EXOC3L2	90332	ENSG00000283632			Exoc3l2 (MGI:1921713)			
chr19	45251257	45305282	19q13.2	19q13.32		606495	"MARK4, KIAA1860, MARKL1"	Map/microtubule affinity-regulating kinase-4	MARK4	57787	ENSG00000007047			Mark4 (MGI:1920955)			
chr19	45306412	45322976	19q13	19q13.32		123310	"CKM, CKMM"	"Creatine kinase, muscle type"	CKM	1158	ENSG00000104879			Ckm (MGI:88413)			
chr19	45340739	45351547	19q13.2-q13.3	19q13.32		601334	"KLC3, KLC2L"	"Kinesin, light chain, 3"	KLC3	147700	ENSG00000104892			Klc3 (MGI:1277971)			
chr19	45349836	45370646	19q13.2-q13.3	19q13.32		126340	"ERCC2, EM9, XPD, COFS2, TTD1"	"Excision repair cross complementing rodent repair deficiency, complementation group-2"	ERCC2	2068	ENSG00000104884	< 250kb from ERCC1; mutation identified in 1 COFS2 patient	"?Cerebrooculofacioskeletal syndrome 2, 610756 (3), Autosomal recessive; Trichothiodystrophy 1, photosensitive, 601675 (3), Autosomal recessive; Xeroderma pigmentosum, group D, 278730 (3), Autosomal recessive"	Ercc2 (MGI:95413)			
chr19	45379633	45406348	19q13.32	19q13.32		607463	"PPP1R13L, RAI, IASPP, NKIP1"	"Protein phosphatase 1, regulatory subunit 13-like"	PPP1R13L	10848	ENSG00000104881			Ppp1r13l (MGI:3525053)			
chr19	45406208	45410765	19q13.2-q13.3	19q13.32		107325	"CD3EAP, ASE1, PAF49"	CD3-epsilon-associated protein	CD3EAP	10849	ENSG00000117877			Cd3eap (MGI:1917583)			
chr19	45407332	45478865	19q13.2-q13.3	19q13.32		126380	"ERCC1, UV20, COFS4"	"Excision repair cross complementing rodent repair deficiency, complementation group-1"	ERCC1	2067	ENSG00000012061	distal to CKM	"Cerebrooculofacioskeletal syndrome 4, 610758 (3), Autosomal recessive"	Ercc1 (MGI:95412)			
chr19	45467994	45475178	19q13.3	19q13.32		164772	FOSB	Oncogene FOS-B	FOSB	2354	ENSG00000125740			Fosb (MGI:95575)			
chr19	45485287	45497054	19q13.3	19q13.32		603183	"RTN2, NSPL1, SPG12"	Reticulon-2	RTN2	6253	ENSG00000125744		"Spastic paraplegia 12, autosomal dominant, 604805 (3), Autosomal dominant"	Rtn2 (MGI:107612)			
chr19	45507429	45526988	19q13.2-q13.3	19q13.32		601703	VASP	Vasodilator-stimulated phosphoprotein	VASP	7408	ENSG00000125753			Vasp (MGI:109268)			
chr19	45527766	45584863	19q13.2-q13.3	19q13.32		606580	"OPA3, MGA3"	OPA3 gene	OPA3	80207	ENSG00000125741		"3-methylglutaconic aciduria, type III, 258501 (3), Autosomal recessive; Optic atrophy 3 with cataract, 165300 (3), Autosomal dominant"	Opa3 (MGI:2686271)			
chr19	45589763	45602207	19q13.2-q13.3	19q13.32		600551	GPR4	G protein-coupled receptor-4	GPR4	2828	ENSG00000177464			Gpr4 (MGI:2441992)			
chr19	45609395	45645628	19q13.32	19q13.32		617494	"EML2, EMAP2, ELP70"	Echinoderm microtubule-associated protein-like 2	EML2	24139	ENSG00000125746			Eml2 (MGI:1919455)			
chr19	45668186	45683723	19q13.3	19q13.32		137241	"GIPR, PGQTL2"	Gastric inhibitory polypeptide receptor	GIPR	2696	ENSG00000010310		"[Plasma glucose, 2-hour, QTL 2], 137241 (2)"	Gipr (MGI:1352753)			
chr19	45687453	45692315	19q13.32	19q13.32		601061	SNRPD2	Small nuclear ribonucleoprotein polypeptide D2	SNRPD2	6633	ENSG00000125743			Snrpd2 (MGI:98345)			
chr19	45710628	45733170	19q13.3	19q13.32		609117	"FBXO46, FBX46"	F-box only protein 46	FBXO46	23403	ENSG00000177051			Fbxo46 (MGI:2444918)			
chr19	45764784	45769238	19q13.3	19q13.32		600963	"SIX5, DMAHP, BOR2"	"Sine oculis homeo box, Drosophila, homolog of, 5"	SIX5	147912	ENSG00000177045		"Branchiootorenal syndrome 2, 610896 (3)"	Six5 (MGI:106220)			
chr19	45769708	45782556	19q13.2-q13.3	19q13.32		605377	"DMPK, DM, DMK"	Dystrophia myotonica-protein kinase	DMPK	1760	ENSG00000104936	distal to APOLP2; distal to CKM	"Myotonic dystrophy 1, 160900 (3), Autosomal dominant"	Dmpk (MGI:94906)			
chr19	45783005	45792801	19q13.3	19q13.32		609857	"DMWD, DMRN9"	Dystrophia myotonica WD repeat-containing protein	DMWD	1762	ENSG00000185800			Dmwd (MGI:94907)			
chr19	45795709	45815346	19q13.3	19q13.32		607548	RSHL1	Radial spokehead-like 1	RSPH6A	81492	ENSG00000104941			Rsph6a (MGI:1927643)			
chr19	45815441	45863289	19q13.3	19q13.32		602388	SPK	Symplekin	SYMPK	8189	ENSG00000125755			Sympk (MGI:1915438)			
chr19	45864259	45873796	19q13.2-q13.4	19q13.32		602295	"FOXA3, HNF3G"	"Forkhead box A3 (hepatocyte nuclear factor-3, gamma)"	FOXA3	3171	ENSG00000170608			Foxa3 (MGI:1347477)			
chr19	45883606	45886169	19q13.32	19q13.32		615331	IRF2BP1	Interferon regulatory factor 2-binding protein 1	IRF2BP1	26145	ENSG00000170604			Irf2bp1 (MGI:2442159)			
chr19	45890019	45902618	19q13.32	19q13.32		617861	MYPOP	"MYB-related transcription factor, partner of profilin"	MYPOP	339344	ENSG00000176182			Mypop (MGI:2446472)			
chr19	45913213	45914777	19q13.32	19q13.32		608228	"NANOS2, NOS2"	"Nanos, Drosophila, homolog of, 2"	NANOS2	339345	ENSG00000188425			Nanos2 (MGI:2676627)			
chr19	45933733	45973398	19q13.3	19q13.32		601991	"NOVA2, ANOVA"	NOVA alternative splicing regulator 2	NOVA2	4858	ENSG00000104967			Nova2 (MGI:104296)			
chr19	46019152	46023297	19q13	19q13.32		604963	"PGRP, PGRPS"	Peptidoglycan recognition protein	PGLYRP1	8993	ENSG00000008438			Pglyrp1 (MGI:1345092)			
chr19	46039747	46041015	19p13.3	19q13.32		610547	IGFL4	IGF-like family member 4	IGFL4	444882	ENSG00000204869						
chr19	46078512	46215361	19p13.3	19q13.32		610545	IGFL2	IGF-like family member 2	IGFL2	147920	ENSG00000204866						
chr19	46119777	46127100	19p13.3	19q13.32		610546	IGFL3	IGF-like family member 3	IGFL3	388555	ENSG00000188624			Igfl3 (MGI:2685426)			
chr19	46229751	46231242	19p13.3	19q13.32		610544	IGFL1	IGF-like family member 1	IGFL1	374918	ENSG00000188293						
chr19	46297045	46343432	19q13.2	19q13.32		609976	"HIF3A, IPAS"	"Hypoxia-inducible factor 3, alpha subunit"	HIF3A	64344	ENSG00000124440			Hif3a (MGI:1859778)			
chr19	46346993	46390974	19q13.3	19q13.32		600658	"PPP5C, PP5"	"Protein phosphatase-5, catalytic subunit"	PPP5C	5536	ENSG00000011485			Ppp5c (MGI:102666)			
chr19	46410328	46413661	19q13.2-q13.32	19q13.32		614145	"CCDC8, 3M3"	Coiled-coil domain-containing protein 8	CCDC8	83987	ENSG00000169515		"3-M syndrome 3, 614205 (3), Autosomal recessive"	Ccdc8 (MGI:3612184)			
chr19	46601073	46610781	19q13.2-q13.3	19q13.32		114183	CALM3	Calmodulin-3	CALM3	808	ENSG00000160014						
chr19	46610039	46625096	19q13.3	19q13.32		600022	PTGIR	Prostaglandin I2 (prostacyclin) receptor (IP)	PTGIR	5739	ENSG00000160013			Ptgir (MGI:99535)			
chr19	46647563	46661137	19q13.3	19q13.32		611112	DACT3	"Dapper, antagonist of beta-catenin, 3"	DACT3	147906	ENSG00000197380			Dact3 (MGI:3654828)			
chr19	46674315	46717126	19q13.3	19q13.32		607074	"PRKD2, PKD2"	Protein kinase D2	PRKD2	25865	ENSG00000105287			Prkd2 (MGI:2141917)			
chr19	46719508	46746474	19q13.32	19q13.32		614767	"STRN4, ZIN"	"Striatin, calmodulin-binding protein 4"	STRN4	29888	ENSG00000090372			Strn4 (MGI:2142346)			
chr19	46746014	46758574	19q13.3	19q13.32		606596	"FKRP, MDC1C, LGMD2I, MDDGA5, MDDGB5, MDDGC5"	Fukutin-related protein	FKRP	79147	ENSG00000181027		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, 613153 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5, 606612 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5, 607155 (3), Autosomal recessive"	Fkrp (MGI:2447586)			
chr19	46759684	46788621	19q13.3	19q13.32		109190	"SLC1A5, RDRC, M7V1, M7VS1"	"Solute carrier family 1 (neutral amino acid transporter), member 5 (receptor for RD114/simian type D retroviruses)"	SLC1A5	6510	ENSG00000105281			Slc1a5 (MGI:105305)			
chr19	46838157	46850994	19q13.2-q13.3	19q13.32		602242	"AP2S1, CLAPS2, AP17, HHC3"	"Adaptor-related protein complex 2, sigma 1 subunit"	AP2S1	1175	ENSG00000042753		"Hypocalciuric hypercalcemia, type III, 600740 (3), Autosomal dominant"	Ap2s1 (MGI:2141861)			
chr19	46918566	47005076	19q13.2-q13.4	19q13.32		605277	"GRLF1, P190A"	Glucocorticoid receptor DNA-binding factor 1	ARHGAP35	2909	ENSG00000160007			Arhgap35 (MGI:1929494)			
chr19	47019843	47045774	19q13.2-q13.3	19q13.32		603346	"NPAS1, MOP5"	Neuronal PAS domain protein 1	NPAS1	4861	ENSG00000130751			Npas1 (MGI:109205)			
chr19	47130793	47210635	19q13.32	19q13.32		613294	"SAE1, SUA1, AOS1"	"SUMO1-activating enzyme, subunit 1"	SAE1	10055	ENSG00000142230			Sae1 (MGI:1929264)			
chr19	47220821	47232997	19q	19q13.32		605854	PUMA	p53-upregulated modulator of apoptosis	BBC3	27113	ENSG00000105327			Bbc3 (MGI:2181667)			
chr19	47309846	47322069	19q13.3-q13.4	19q13.32		113995	"C5AR1, C5R1, C5AR"	Complement component 5a receptor 1	C5AR1	728	ENSG00000197405			C5ar1 (MGI:88232)			
chr19	47331613	47342079	19q13.4	19q13.32		609949	"C5AR2, GPF77, C5L2"	Complement component 5a receptor 2	C5AR2	27202	ENSG00000134830			C5ar2 (MGI:2442013)			
chr19	47349280	47382703	19q13.32	19q13.32		615475	"DHX34, KIAA0134"	DEAH box polypeptide 34	DHX34	9704	ENSG00000134815			Dhx34 (MGI:1918973)			
chr19	47428016	47472049	19q13.32	19q13.32		601901	"SLC8A2, NCX2"	"Solute carrier family 8, member 2 (sodium-calcium exchanger 2)"	SLC8A2	6543	ENSG00000118160			Slc8a2 (MGI:107996)			
chr19	47475140	47486791	19q13.4	19q13.32		615620	"KPTN, 2E4, MRT41"	Kaptin	KPTN	11133	ENSG00000118162		"Mental retardation, autosomal recessive 41, 615637 (3), Autosomal recessive"	Kptn (MGI:1890380)			
chr19	47487633	47515257	19q13.3	19q13.32-q13.33		603215	"NAPA, SNAPA"	"N-ethylmaleimide-sensitive factor attachment protein, alpha"	NAPA	8775	ENSG00000105402			Napa (MGI:104563)			
chr19	47608195	47703276	19q13.3	19q13.33		605690	GLTSCR1	Glioma tumor suppressor candidate region gene 1	BICRA	29998	ENSG00000063169			Bicra (MGI:2154263)			
chr19	47713343	47743133	19q13.3	19q13.33		605890	EHD2	EH domain-containing 2	EHD2	30846	ENSG00000024422			Ehd2 (MGI:2154274)			
chr19	47745535	47757065	19q13.3	19q13.33		605691	GLTSCR2	Glioma tumor suppressor candidate region gene 2	NOP53	29997	ENSG00000105373			Nop53 (MGI:2154441)			
chr19	47778571	47784680	19q13.3	19q13.33		603235	"SELENOW, SEPW1"	Selenoprotein W	SELENOW	6415	ENSG00000178980			Selenow (MGI:1100878)			
chr19	47801242	47803603	19q13.32	19q13.33		611166	TPRX1	Tetrapeptide repeat homeobox 1	TPRX1	284355	ENSG00000178928						
chr19	47821839	47843329	19q13.3	19q13.33		602225	"CRX, CORD2, CRD, LCA7"	Cone-rod homeo box-containing gene	CRX	1406	ENSG00000105392		"Cone-rod retinal dystrophy-2, 120970 (3), Autosomal dominant; Leber congenital amaurosis 7, 613829 (3)"	Crx (MGI:1194883)			
chr19	47870465	47886396	19q13.3	19q13.33		125263	"SULT2A1, STD"	"Sulfotransferase family 2A, dehydroepiandrosterone-preferring, member 1 (DHEA sulfotransferase)"	SULT2A1	6822	ENSG00000105398			"Sult2a4,Sult2a3,Sult2a1,Sult2a6,Sult2a5 (MGI:98430,MGI:3645854,MGI:3648915,MGI:3648378,MGI:3645873)"			
chr19	47967257	47992169	19q13.32	19q13.33		612213	BSPH1	Bovine seminal plasma protein-like 1	BSPH1	100131137	ENSG00000188334			Bsph1 (MGI:2685613)			
chr19	47994650	48025152	19q13.33	19q13.33		607443	ELSPBP1	Epididymal sperm binding protein 1	ELSPBP1	64100	ENSG00000169393						
chr19	48029382	48048341	19q13.33	19q13.33		607315	"CABP5, CABP3"	Calcium-binding protein 5	CABP5	56344	ENSG00000105507			Cabp5 (MGI:1352746)			
chr19	48047842	48111382	19q13.3	19q13.33		603602	PLA2G4C	"Phospholipase A2, group IVC"	PLA2G4C	8605	ENSG00000105499			Pla2g4c (MGI:1196403)			
chr19	48115444	48170602	19q13.2-q13.3	19q13.33		126391	LIG1	"Ligase I, DNA, ATP-dependent"	LIG1	3978	ENSG00000105486		DNA ligase I deficiency (3)	Lig1 (MGI:101789)			
chr19	48203147	48256263	19q13.3	19q13.33		609051	"CARD8, TUCAN, KIAA0955, NDPP1"	Caspase recruitment domain-containing protein 8	CARD8	22900	ENSG00000105483						
chr19	48270098	48287607	19q13.33	19q13.33		603996	ZNF114	Zinc finger protein-114	ZNF114	163071	ENSG00000178150						
chr19	48296451	48322792	19q13.3	19q13.33		615038	"CCDC114, CILD20"	Coiled-coil domain-containing protein 114	CCDC114	93233	ENSG00000105479		"Ciliary dyskinesia, primary, 20, 615067 (3), Autosomal recessive"	Ccdc114 (MGI:2446120)			
chr19	48325371	48330553	19q13.3	19q13.33		602335	EMP3	Epithelial membrane protein 3	EMP3	2014	ENSG00000142227			Emp3 (MGI:1098729)			
chr19	48364266	48376376	19q13.3	19q13.33		608373	SYNGR4	Synaptogyrin 4	SYNGR4	23546	ENSG00000105467			Syngr4 (MGI:1928903)			
chr19	48382569	48391552	19q13.33	19q13.33		131235	"KDELR1, ERD2, HDEL"	KDEL endoplasmic reticulum protein retention receptor 1	KDELR1	10945	ENSG00000105438			Kdelr1 (MGI:1915387)			
chr19	48394874	48444936	19q13.1-qter	19q13.33		602717	"GRIN2D, NMDAR2D, EIEE46"	"Glutamate receptor, ionotropic, N-methyl-D-aspartate 2D"	GRIN2D	2906	ENSG00000105464		"Epileptic encephalopathy, early infantile, 46, 617162 (3), Autosomal dominant"	Grin2d (MGI:95823)			
chr19	48445772	48453906	19q13.3	19q13.33		610597	"GRWD1, GRWD, KIAA1942"	Glutamate-rich WD repeat-containing protein 1	GRWD1	83743	ENSG00000105447			Grwd1 (MGI:2141989)			
chr19	48469207	48482313	19q13	19q13.33		602488	"CYTH2, PSCD2, ARNO, PSCD2L"	Cytohesin 2	CYTH2	9266	ENSG00000105443			Cyth2 (MGI:1334255)			
chr19	48552171	48599426	19q13.3	19q13.33		604125	"SULT2B1, ARCI14"	"Sulfotransferase family 2B, member 1"	SULT2B1	6820	ENSG00000088002		"Ichthyosis, congenital, autosomal recessive 14, 617571 (3), Autosomal recessive"	Sult2b1 (MGI:1926342)			
chr19	48606742	48607713	19q13.33	19q13.33		609932	"SPACA4, SAMP14"	Sperm acrosome-associated protein 4	SPACA4	171169	ENSG00000177202			Spaca4 (MGI:1916613)			
chr19	48615326	48619417	19q	19q13.33		604179	RPL18	Ribosomal protein L18	RPL18	6141	ENSG00000063177			Rpl18 (MGI:98003)			
chr19	48619290	48630406	19q13.2	19q13.33		607092	SPHK2	Sphingosine kinase 2	SPHK2	56848	ENSG00000063176			Sphk2 (MGI:1861380)			
chr19	48630559	48637549	19q13.3	19q13.33		124097	DBP	D site of albumin promoter binding protein	DBP	1628	ENSG00000105516			Dbp (MGI:94866)			
chr19	48637941	48646311	19q13.2-q13.3	19q13.33		604644	"CA11, CARP2"	Carbonic anhydrase XI	CA11	770	ENSG00000063180			Car11 (MGI:1336193)			
chr19	48695970	48705933	19q13.3	19q13.33		182100	"FUT2, SE, B12QTL1"	Fucosyltransferase-2 (secretor)	FUT2	2524	ENSG00000176920	"H, SE = alpha-L-fucosyltransferases; from common ancestral genes; tightly linked to FUT1"	"[Bombay phenotype] (3); {Norwalk virus infection, resistance to} (3); {Vitamin B12 plasma level QTL1}, 612542 (3)"	Fut2 (MGI:109374)			
chr19	48712440	48719897	19q13.33	19q13.33		610349	"MAMSTR, MASTR"	MEF2-activating SAP transcriptional regulator	MAMSTR	284358	ENSG00000176909			Mamstr (MGI:1921740)			
chr19	48720584	48740832	19q13.33	19q13.33		609623	"RASIP1, RAIN"	Ras-interacting protein 1	RASIP1	54922	ENSG00000105538			Rasip1 (MGI:1917153)			
chr19	48740887	48746908	19q13.33	19q13.33		609278	"IZUMO1, MGC34799"	Izumo sperm-egg fusion protein 1	IZUMO1	284359	ENSG00000182264			Izumo1 (MGI:1920706)			
chr19	48748010	48755389	19q13.3	19q13.33		211100	"FUT1, H, HH"	Fucosyltransferase-1 (Bombay phenotype)	FUT1	2523	ENSG00000174951	SE tightly linked	"[Bombay phenotype], 616754 (3), Autosomal recessive"	Fut1 (MGI:109375)			
chr19	48755558	48758329	19q13	19q13.33		609436	FGF21	Fibroblast growth factor 21	FGF21	26291	ENSG00000105550			Fgf21 (MGI:1861377)			
chr19	48795061	48811062	19q13	19q13.33		113530	"BCAT2, BCT2"	"Branched chain aminotransferase-2, mitochondrial"	BCAT2	587	ENSG00000105552		?Hypervalinemia or hyperleucine-isoleucinemia (1)	Bcat2 (MGI:1276534)			
chr19	48813013	48836687	19q13.33	19q13.33		612832	"HSD17B14, DHRS10, RETSDR3"	17-beta-hydroxysteroid dehydrogenase XIV	HSD17B14	51171	ENSG00000087076			Hsd17b14 (MGI:1913315)			
chr19	48837091	48868626	19q13.33	19q13.33		607769	"PLEKHA4, PEPP1"	"Pleckstrin homology domain-containing protein, family A, member 4"	PLEKHA4	57664	ENSG00000105559			Plekha4 (MGI:1916467)			
chr19	48872391	48876061	19q13.2	19q13.33		611048	"PPP1R15A, GADD34"	"Protein phosphatase 1, regulatory subunit 15A"	PPP1R15A	23645	ENSG00000087074			Ppp1r15a (MGI:1927072)			
chr19	48880816	48900220	19q13.1	19q13.33		602309	TULP2	Tubby-like protein-2	TULP2	7288	ENSG00000104804			Tulp2 (MGI:1861600)			
chr19	48900049	48923282	19q13.2-q13.4	19q13.33		601323	NUCB1	Nucleobindin 1	NUCB1	4924	ENSG00000104805			Nucb1 (MGI:97388)			
chr19	48954824	48961797	19q13.3-q13.4	19q13.33		600040	BAX	BCL2-associated X protein	BAX	581	ENSG00000087088		"Colorectal cancer, somatic, 114500 (3); T-cell acute lymphoblastic leukemia, somatic, 613065 (3)"	Bax (MGI:99702)			
chr19	48963940	48966878	19q13.3-q13.4	19q13.33		134790	"FTL, NBIA3, LFTD"	"Ferritin, light chain"	FTL	2512	ENSG00000087086		"Hyperferritinemia-cataract syndrome, 600886 (3), Autosomal dominant; L-ferritin deficiency, dominant and recessive, 615604 (3), Autosomal recessive, Autosomal dominant; Neurodegeneration with brain iron accumulation 3, 606159 (3), Autosomal dominant"	"Ftl1,Ftl1-ps2 (MGI:5434102,MGI:95589)"			
chr19	48968124	48993352	19q13.3	19q13.33		138570	"GYS1, GYS"	Glycogen synthase	GYS1	2997	ENSG00000104812		"Glycogen storage disease 0, muscle, 611556 (3), Autosomal recessive"	Gys1 (MGI:101805)			
chr19	48993447	49015994	19q13.3	19q13.33		604788	"RUVBL2, TIP48, ECP51"	"RUVB, E. coli, homolog-like 2 (TATA box-binding protein-interacting protein)"	RUVBL2	10856	ENSG00000183207			Ruvbl2 (MGI:1342299)			
chr19	49015979	49017089	19q13.32	19q13.33		152780	"LHB, HH23"	"Luteinizing hormone, beta polypeptide"	LHB	3972	ENSG00000104826	"beta chains of FSH, TSH on 11p, 1p, respectively"	"Hypogonadotropic hypogonadism 23 with or without anosmia, 228300 (3), Autosomal recessive"	Lhb (MGI:96782)			
chr19	49022868	49024374	19q13.32	19q13.33		118860	CGB	"Chorionic gonadotropin, beta polypeptide"	CGB3	1082	ENSG00000104827	at least 5 genes					
chr19	49035568	49036933	19q13.33	19q13.33		608823	CGB1	"Chorionic gonadotropin, beta polypeptide 1"	CGB1	114335	ENSG00000267631						
chr19	49054273	49057247	19q13.33	19q13.33		608826	"CGB7, CGB6"	"Chorionic gonadotropin, beta polypeptide 7"	CGB7	94027	ENSG00000196337						
chr19	49058283	49065075	19q13.3	19q13.33		162662	"NTF4 , NTF5, NT5, NT4, GLC1O"	Neurotrophin-4 (neurotrophin-4/5)	NTF4	4909	ENSG00000225950	"3 genes, ? functional, also on 19"	"Glaucoma 1, open angle, 1O, 613100 (3)"	Ntf5 (MGI:97381)			
chr19	49067417	49072940	19q13.3	19q13.33		176268	KCNA7	"Potassium voltage-gated channel, shaker-related subfamily, member 7"	KCNA7	3743	ENSG00000104848			Kcna7 (MGI:96664)			
chr19	49085139	49108612	19q13.3	19q13.33		180740	"SNRP70, U1RNP, RNPU1Z, RPU1"	"Small nuclear ribonucleoprotein, U1 subunit, 70kD"	SNRNP70	6625	ENSG00000104852			Snrnp70 (MGI:98341)			
chr19	49114338	49118463	19q13.33	19q13.33		612331	"LIN7B, VELI2, MALS2"	"Lin7, C. elegans, homolog of, B"	LIN7B	64130	ENSG00000104863			Lin7b (MGI:1330858)			
chr19	49119388	49151029	19q13.33	19q13.33		603144	"PPFIA3, LPNA3"	"Protein tyrosine phosphatase, receptor type, f polypeptide (liprin-alpha-3)"	PPFIA3	8541	ENSG00000177380			Ppfia3 (MGI:1924037)			
chr19	49151197	49155463	19q13.3	19q13.33		142705	HRC	Histidine-rich calcium-binding protein	HRC	3270	ENSG00000130528						
chr19	49157740	49211840	19q13.32	19q13.33		606936	"TRPM4, PFHB1B"	"Transient receptor potential cation channel, subfamily M, member 4"	TRPM4	54795	ENSG00000130529		"Progressive familial heart block, type IB, 604559 (3), Autosomal dominant"	Trpm4 (MGI:1915917)			
chr19	49289631	49332319	19q13.33	19q13.33		607972	"SLC6A16, NT5"	"Solute carrier family 6 (neurotransmitter transporter), member 16"	SLC6A16	28968	ENSG00000063127			Slc6a16 (MGI:2685930)			
chr19	49334960	49340607	19p13-q13.4	19q13.33		151523	CD37	Leukocyte surface antigen CD37	CD37	951	ENSG00000104894			Cd37 (MGI:88330)			
chr19	49340594	49362456	19q13.3	19q13.33		601729	"TEAD2, TEF4"	TEA domain family member 2	TEAD2	8463	ENSG00000074219			Tead2 (MGI:104904)			
chr19	49360519	49375131	19q13.33	19q13.33		605418	"DKKL1, SGY1, SGY"	Dickkopf-like 1	DKKL1	27120	ENSG00000104901			Dkkl1 (MGI:1354963)			
chr19	49422413	49423440	19q13.33	19q13.33		608386	"PTH2, TIP39"	Parathyroid hormone 2	PTH2	113091	ENSG00000142538			Pth2 (MGI:2152297)			
chr19	49429397	49441550	19q13	19q13.33		605208	"SLC17A7, BNPI, VGLUT1"	"Solute carrier family 17, (sodium-dependent inorganic phosphate cotransporter), member 7"	SLC17A7	57030	ENSG00000104888			Slc17a7 (MGI:1920211)			
chr19	49446292	49452391	19q13.33	19q13.33		611480	"PIH1D1, NOP17"	PIH1 domain-containing protein 1	PIH1D1	55011	ENSG00000104872			Pih1d1 (MGI:1916095)			
chr19	49453215	49471049	19q13.33	19q13.33		613358	ALDH16A1	"Aldehyde dehydrogenase 16 family, member A1"	ALDH16A1	126133	ENSG00000161618			Aldh16a1 (MGI:1916998)			
chr19	49474171	49487036	19q13.33	19q13.33		600007	"FLT3LG, FLG3L"	FMS-related tyrosine kinase 3 ligand	FLT3LG	2323	ENSG00000090554			Flt3l (MGI:95560)			
chr19	49496364	49499711	19q	19q13.33		180471	RPS11	Ribosomal protein S11	RPS11	6205	ENSG00000142534			Rps11 (MGI:1351329)			
chr19	49500784	49500867	19q13.33	19q13.33		611114	"MIR150, MIRN150"	Micro RNA 150	MIR150	406942							
chr19	49512278	49526427	19q13.3	19q13.33		601437	FCGRT	"Fc fragment of IgG, receptor, transporter, alpha"	FCGRT	2217	ENSG00000104870			Fcgrt (MGI:103017)			
chr19	49555467	49580571	19q13.33	19q13.33		616759	NOSIP	Nitric oxide synthase-interacting protein	NOSIP	51070	ENSG00000142546			Nosip (MGI:1913644)			
chr19	49580616	49591007	19q13.33	19q13.33		604429	"PRRG2, PRGP2"	Proline-rich gamma-carboxyglutamic acid protein 2	PRRG2	5639	ENSG00000126460			Prrg2 (MGI:1929596)			
chr19	49591176	49626438	19q13.33	19q13.33		616633	"PRR12, KIAA1205"	Proline-rich protein 12	PRR12	57479	ENSG00000126464			Prr12 (MGI:2679002)			
chr19	49635291	49640142	19q13.3-qter	19q13.33		165090	RRAS	Oncogene RRAS	RRAS	6237	ENSG00000126458			Rras (MGI:98179)			
chr19	49640480	49658648	19q13.3	19q13.33		617264	SCAF1	SR-related C-terminal domain-associated factor 1	SCAF1	58506	ENSG00000126461						
chr19	49659568	49665874	19q13.3-q13.4	19q13.33		603734	"IRF3, IIAE7"	Interferon regulatory factor 3	IRF3	3661	ENSG00000126456		"{Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7}, 616532 (3), Autosomal dominant"	Irf3 (MGI:1859179)			
chr19	49664833	49673915	19q13.3	19q13.33		610837	BCL2L12	BCL2-like 12	BCL2L12	83596	ENSG00000126453			Bcl2l12 (MGI:1922986)			
chr19	49676165	49688449	19q13	19q13.33		602950	"PRMT1, HRMT1L2, IR1B4"	Protein arginine methyltransferase 1	PRMT1	3276	ENSG00000126457			Prmt1 (MGI:107846)			
chr19	49690671	49713730	19q13.33	19q13.33		608846	"CPT1C, SPG73"	Carnitine palmitoyltransferase IC	CPT1C	126129	ENSG00000169169	mutation identified in 1 SPG73 family	"?Spastic paraplegia 73, autosomal dominant, 616282 (3), Autosomal dominant"	Cpt1c (MGI:2446526)			
chr19	49766922	49807113	19q13.3	19q13.33		601026	"AP2A1, CLAPA1, ADTAA"	"Adaptor-related protein complex 2, alpha 1 subunit"	AP2A1	160	ENSG00000196961	match to PAC AC006942		Ap2a1 (MGI:101921)			
chr19	49806865	49817375	19q13	19q13.33		610622	"FUZ, NTD"	"Fuzzy, Drosophila, homolog of"	FUZ	80199	ENSG00000010361		"Neural tube defects, 182940 (3), Autosomal dominant"	Fuz (MGI:1917550)			
chr19	49818278	49840383	19q13.3	19q13.33		610197	"MED25, PTOV2, ARC92, CMT2B2, BVSYS"	"Mediator of RNA polymerase II transcription, subunit 25, S. cerevisiae, homolog of"	MED25	81857	ENSG00000104973	mutation identified in 1 CMT2B2 family	"Basel-Vanagait-Smirin-Yosef syndrome, 616449 (3), Autosomal recessive; ?Charcot-Marie-Tooth disease, type 2B2, 605589 (3), Autosomal recessive"	Med25 (MGI:1922863)			
chr19	49848553	49860743	19q13.3-q13.4	19q13.33		610195	"PTOV1, ACID2"	Prostate tumor overexpressed gene 1	PTOV1	53635	ENSG00000104960			Ptov1 (MGI:1933946)			
chr19	49861202	49867564	19q13.4	19q13.33		605610	"PNKP, PNK, MCSZ, EIEE10, AOA4"	Polynucleotide kinase 3' phosphatase	PNKP	11284	ENSG00000039650		"Ataxia-oculomotor apraxia 4, 616267 (3), Autosomal recessive; Microcephaly, seizures, and developmental delay, 613402 (3), Autosomal recessive"	Pnkp (MGI:1891698)			
chr19	49877424	49888749	19q13.33	19q13.33		616659	TBC1D17	"TBC1 domain family, member 17"	TBC1D17	79735	ENSG00000104946			Tbc1d17 (MGI:2449973)			
chr19	49889653	49929538	19q13.3-q13.4	19q13.33		609742	"IL4I1, FIG1"	Interleukin 4-induced gene 1	IL4I1	259307	ENSG00000104951			"Gm21948,Il4i1 (MGI:5439399,MGI:109552)"			
chr19	49906824	49929730	19q13.33	19q13.33		605815	"NUP62, SNDI, IBSN"	"Nucleoporin, 62-kD"	NUP62	23636	ENSG00000213024		"Striatonigral degeneration, infantile, 271930 (3), Autosomal recessive"	Nup62 (MGI:1351500)			
chr19	49928701	49933935	19q13.3	19q13.33		606398	"ATF5, ATFX"	Activating transcription factor 5	ATF5	22809	ENSG00000169136			Atf5 (MGI:2141857)			
chr19	49948824	49961171	19q13.3-q13.4	19q13.33		607157	SIGLEC11	Sialic acid-binding immunoglobulin-like lectin 11	SIGLEC11	114132	ENSG00000161640	pseudogene 8kb upstream					
chr19	50025892	50048775	19q13.33	19q13.33		617908	"ZNF473, ZFP100, KIAA1141"	Zinc finger protein 473	ZNF473	25888	ENSG00000142528			Zfp473 (MGI:2442697)			
chr19	50188185	50310543	19q13.33	19q13.33		608568	"MYH14, KIAA2034, DFNA4A, PNMHH"	"Myosin, heavy chain 14, nonmuscle"	MYH14	79784	ENSG00000105357	mutation identified in 1 PNMHH family	"Deafness, autosomal dominant 4A, 600652 (3), Autosomal dominant; ?Peripheral neuropathy, myopathy, hoarseness, and hearing loss, 614369 (3), Autosomal dominant"	Myh14 (MGI:1919210)			
chr19	50311941	50333514	19q13.3-q13.4	19q13.33		176264	"KCNC3, SCA13"	"Potassium voltage-gated channel, Shaw-related subfamily, member 3"	KCNC3	3748	ENSG00000131398		"Spinocerebellar ataxia 13, 605259 (3), Autosomal dominant"	Kcnc3 (MGI:96669)			
chr19	50358471	50369330	19q13.33	19q13.33		605631	"NAPA, NAP1, SNAPA"	Napsin A	NAPSA	9476	ENSG00000131400			Napsa (MGI:109365)			
chr19	50376422	50383027	19q13.3	19q13.33		600380	"NR1H2, UNR"	"Nuclear receptor subfamily 1, group H, member 2 (ubiquitously-expressed nuclear receptor)"	NR1H2	7376	ENSG00000131408			Nr1h2 (MGI:1352463)			
chr19	50384290	50418017	19q13.3-q13.4	19q13.33		174761	"POLD1, CRCS10, MDPL"	"Polymerase (DNA directed), delta 1, catalytic subunit"	POLD1	5424	ENSG00000062822		"{Colorectal cancer, susceptibility to, 10}, 612591 (3), Autosomal dominant; Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, 615381 (3), Autosomal dominant"	Pold1 (MGI:97741)			
chr19	50418937	50431052	19q13.3-q13.4	19q13.33		606802	SPIB	SPIB transcription factor	SPIB	6689	ENSG00000269404			Spib (MGI:892986)			
chr19	50432902	50466325	19q13.33	19q13.33		160793	"MYBPC2, MYBPCF"	"Myosin-binding protein C, fast type"	MYBPC2	4606	ENSG00000086967			Mybpc2 (MGI:1336170)			
chr19	50476476	50505904	19q13.33	19q13.33		614545	"EMC10, C19orf63, HSS1, HSM1"	ER membrane protein complex subunit 10	EMC10	284361	ENSG00000161671			Emc10 (MGI:1916933)			
chr19	50505996	50511354	19q13.33	19q13.33		615324	JOSD2	Josephin domain-containing protein 2	JOSD2	126119	ENSG00000161677			Josd2 (MGI:1913374)			
chr19	50621976	50658113	19q	19q13.33		600327	SYT3	Synaptotagmin-3	SYT3	84258	ENSG00000213023			Syt3 (MGI:99665)			
chr19	50659256	50719782	19q13.33	19q13.33		604999	"SHANK1, SSTRIP"	SH3 and multiple ankyrin repeat domains 1	SHANK1	50944	ENSG00000161681			Shank1 (MGI:3613677)			
chr19	50723347	50725723	19q13.3	19q13.33		604713	"CLEC11A, SCGF, LSLCL"	"C-type lectin domain family 11, member A"	CLEC11A	6320	ENSG00000105472			Clec11a (MGI:1298219)			
chr19	50770463	50771731	19q13.3	19q13.33		603195	GPR32	G protein-coupled receptor-32	GPR32	2854	ENSG00000142511						
chr19	50790414	50795223	19q13	19q13.33		606362	"ACPT, AI1J"	"Acid phosphatase, testicular"	ACP4	93650	ENSG00000142513		"Amelogenesis imperfecta, type IJ, 617297 (3), Autosomal recessive"	Acp4 (MGI:3644563)			
chr19	50819145	50823786	19q13.4	19q13.33		147910	"KLK1, KLKR"	Kallikrein 1	KLK1	3816	ENSG00000167748	~10cM distal to APOC2	"[Kallikrein, decreased urinary activity of], 615953 (3)"				
chr19	50825288	50834336	19q13.4	19q13.33		610601	KLK15	Kallikrein-related peptidase 15	KLK15	55554	ENSG00000174562			Klk15 (MGI:2447533)			
chr19	50854914	50860763	19q13.4	19q13.33		176820	"KLK3, APS, PSA"	Kallikrein-related peptidase 3	KLK3	354	ENSG00000142515	"probably with cluster KLK1, KLK2"		"Klk1b21,Klk1b9,Klk1b11,Klk1b22,Klk1b8,Klk1,Klk1b5,Klk1b26,Klk1b3,Klk1b24,Klk1b4,Klk1b1,Klk1b16,Klk1b27 (MGI:102850,MGI:95293,MGI:95291,MGI:892019,MGI:892018,MGI:97320,MGI:97322,MGI:892023,MGI:892022,MGI:892021,MGI:892020,MGI:891982,MGI:891980,MGI:891981)"			
chr19	50873432	50880566	19q13.4	19q13.33		147960	KLK2	Kallikrein-related peptidase 2	KLK2	3817	ENSG00000167751	12kb from APS					
chr19	50900000	58617616	19q13.4-qter			102699	AAVS1	Adeno-associated virus integration site-1	AAVS1	17							
chr19	50900000	58617616	19q13.4			611959	HPC15	"Prostate cancer, hereditary, 15"		100188868		associated with rs2735839	"{Prostate cancer, hereditary, 15}, 611959 (2)"				
chr19	50900000	58617616	19q13.4			604937	"KIR2DL2, NKAT6"	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2"	KIR2DL2	3803							
chr19	50900000	58617616	19q13.4			615727	KIR2DL5B	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B"	KIR2DL5B	553128							
chr19	50900000	58617616	19q13.4			604952	KIR2DS1	"Killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 1"	KIR2DS1	3806							
chr19	50900000	58617616	19q13.4			604953	"KIR2DS2, NKAT5"	"Killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2"	KIR2DS2	100132285							
chr19	50900000	58617616	19q13.4			604954	"KIR2DS3, NKAT7"	"Killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 3"	KIR2DS3	3808							
chr19	50900000	58617616	19q13.4			604956	"KIR2DS5, NKAT9, CD158G"	"Killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 5"	KIR2DS5	3810							
chr19	50900000	58617616	19q13.4			604818	"LILRA3, LIR4, ILT6, HM43"	"Leukocyte immunoglobulin-like receptor, subfamily A, member 3"	LILRA3	11026							
chr19	50900000	58617616	19q13.4			612884	MENOQ2	"Menopause, natural, age at, QTL2"		100302517		"associated with rs1172822, rs2384687, rs1551562, rs897798"	"{Menopause, natural, age at, QTL2}, 612884 (2)"				
chr19	50906351	50910744	19q13.4	19q13.41		603767	"KLK4, EMSP1, PRSS17, AI2A1"	Kallikrein-related peptidase 4	KLK4	9622	ENSG00000167749		"Amelogenesis imperfecta, type IIA1, 204700 (3), Autosomal recessive"	Klk4 (MGI:1861379)			
chr19	50943298	50953087	19q13.4	19q13.41		605643	"KLK5, SCTE, KLKL2"	Kallikrein-related peptidase 5	KLK5	25818	ENSG00000167754			Klk5 (MGI:1915918)			
chr19	50958630	50969672	19q13.4	19q13.41		602652	"KLK6, PRSS9, ZYME"	Kallikrein-related peptidase 6	KLK6	5653	ENSG00000167755			Klk6 (MGI:1343166)			
chr19	50976478	50984063	19q13.41	19q13.41		604438	"LKL7, PRSS6, SCCE"	Kallikrein-related peptidase 7	KLK7	5650	ENSG00000169035			Klk7 (MGI:1346336)			
chr19	50996007	51001701	19q13.4	19q13.41		605644	"KLK8, TADG14, PRSS19"	Kallikrein-related peptidase 8	KLK8	11202	ENSG00000129455			Klk8 (MGI:1343327)			
chr19	51002512	51009633	19q13.4	19q13.41		605504	"KLK9, KLKL3"	Kallikrein-related peptidase 9	KLK9	284366	ENSG00000213022			Klk9 (MGI:1921082)			
chr19	51012743	51020174	19q13.4	19q13.41		602673	"KLK10, PRSSL1, NES1"	Kallikrein-related peptidase 10	KLK10	5655	ENSG00000129451			Klk10 (MGI:1916790)			
chr19	51022230	51028033	19q13.4	19q13.41		604434	"KLK11, PRSS20, TLSP"	Kallikrein-related peptidase 11	KLK11	11012	ENSG00000167757			Klk11 (MGI:1929977)			
chr19	51028953	51035649	19q13.4	19q13.41		605539	"KLK12, KLKL5"	Kallikrein-related peptidase 12	KLK12	43849	ENSG00000186474			Klk12 (MGI:1916761)			
chr19	51055625	51065109	19q13.4	19q13.41		605505	"KLK13, KLKL4"	Kallikrein-related peptidase 13	KLK13	26085	ENSG00000167759			Klk13 (MGI:3615275)			
chr19	51077494	51084209	19q13.4	19q13.41		606135	KLK14	Kallikrein-related peptidase 14	KLK14	43847	ENSG00000129437			Klk14 (MGI:2447564)			
chr19	51097605	51108389	19q13.33	19q13.41		612694	"CTU1, ATPBD3"	Cytothiouridylase subunit 1	CTU1	90353	ENSG00000142544			Ctu1 (MGI:2385277)			
chr19	51124879	51140479	19q13.4	19q13.41		605640	SIGLEC9	Sialic acid-binding immunoglobulin-like lectin 9	SIGLEC9	27180	ENSG00000129450			Siglece (MGI:1932475)			
chr19	51142259	51153525	19q13.3	19q13.41		604410	"SIGLEC7, AIRM1"	Sialic acid-binding immunoglobulin-like lectin 7	SIGLEC7	27036	ENSG00000168995						
chr19	51211053	51240018	19q13.3-q13.4	19q13.41		159590	CD33	CD33 antigen (gp67)	CD33	945	ENSG00000105383						
chr19	51331535	51342123	19q13.41	19q13.41		617740	VSIG10L	V-set and immunoglobulin domains-containing protein 10-like	VSIG10L	147645	ENSG00000186806			Vsig10l (MGI:1922940)			
chr19	51345154	51366417	19q13.3	19q13.41		130410	"ETFB, MADD"	"Electron transfer flavoprotein, beta polypeptide"	ETFB	2109	ENSG00000105379		"Glutaric acidemia IIB, 231680 (3), Autosomal recessive"	Etfb (MGI:106098)			
chr19	51379908	51387955	19q13.4	19q13.41		154045	"LIM2, MP19, CTRCT19"	"Lens intrinsic protein 2, 19kD"	LIM2	3982	ENSG00000105370	same cosmid as ETFB	"Cataract 19, multiple types, 615277 (3), Autosomal recessive"	Lim2 (MGI:104698)			
chr19	51410020	51417802	19q13.4	19q13.41		606091	SIGLEC10	Sialic acid-binding immunoglobulin-like lectin 10	SIGLEC10	89790	ENSG00000142512			Siglecg (MGI:2443630)			
chr19	51450996	51458453	19q13.33-q13.41	19q13.41		605639	"SIGLEC8, SAF2, SIGLEC8L"	Sialic acid-binding immunoglobulin-like lectin 8	SIGLEC8	27181	ENSG00000105366			Siglecf (MGI:2681107)			
chr19	51491226	51501788	19q13.4	19q13.41		606094	"SIGLEC12, SIGLECL1, S2V, SLG"	Sialic acid-binding immunoglobulin-like lectin 12	SIGLEC12	89858	ENSG00000254521						
chr19	51517818	51531855	19q13.3	19q13.41		604405	"SIGLEC6, CD33L, CD33L1, OBBP1"	Sialic acid-binding immunoglobulin-like lectin 6	SIGLEC6	946	ENSG00000105492						
chr19	51571236	51589737	19q13.4	19q13.41		601139	"ZNF175, OTK18"	Zinc finger protein-175	ZNF175	7728	ENSG00000105497			Zfp715 (MGI:1917180)			
chr19	51610966	51630473	19q13.3	19q13.41		604200	"SIGLEC5, CD33L2, OBBP2"	Sialic acid-binding Ig-like lectin 5	SIGLEC5	8778	ENSG00000105501						
chr19	51692611	51692680	19q13.41	19q13.41		614510	MIR99B	Micro RNA 99B	MIR99B	407056							
chr19	51692785	51692863	19q13.41	19q13.41		611250	"MIRLET7E, LET7E"	Micro RNA Let7e	MIRLET7E	406887							
chr19	51693253	51693338	19q13.33	19q13.41		611191	"MIR125A, MIRN125A"	Micro RNA 125A	MIR125A	406910							
chr19	51713111	51723991	19q13.3-q13.4	19q13.41		601463	HAS1	Hyaluronan synthase 1	HAS1	3036	ENSG00000105509			Has1 (MGI:106590)			
chr19	51745769	51751896	19q13.4	19q13.41		136537	FPR1	Formyl peptide receptor-1	FPR1	2357	ENSG00000171051			Fpr1 (MGI:107443)			
chr19	51752025	51770525	19q13.3-q13.4	19q13.41		136538	"FPR2, FPRL1, FPRH1, LXA4R, HM63"	Formyl peptide receptor 2	FPR2	2358	ENSG00000171049			Fpr2 (MGI:1278319)			
chr19	51795145	51826206	19q13.3-q13.4	19q13.41		136539	"FPR3, FPRL2, FPRH2"	Formyl peptide receptor 3	FPR3	2359	ENSG00000187474						
chr19	51889234	51905051	19q13.41	19q13.41		611903	ZNF649	Zinc finger protein 649	ZNF649	65251	ENSG00000198093						
chr19	51964339	51986855	19q13.41	19q13.41		605422	"ZNF350, ZBRK1"	Zinc finger protein 350	ZNF350	59348	ENSG00000256683						
chr19	52189801	52226424	19q13.4	19q13.41		605983	"PPP2R1A, MRD36"	"Protein phosphatase 2, structural/regulatory subunit A, alpha"	PPP2R1A	5518	ENSG00000105568		"Mental retardation, autosomal dominant 36, 616362 (3), Autosomal dominant"	Ppp2r1a (MGI:1926334)			
chr19	52297168	52325926	19q13.41	19q13.41		613910	ZNF480	Zinc finger protein 480	ZNF480	147657	ENSG00000198464						
chr19	52392751	52418407	19q13.41	19q13.41		615580	"ZNF528, KIAA1827"	Zinc finger protein 528	ZNF528	84436	ENSG00000167555						
chr19	52596683	52600151	19q13.3-q13.4	19q13.41		604079	ZNF137	Zinc finger protein-137	ZNF137P	7696							
chr19	52612363	52690580	19q13.3-q13.4	19q13.41		194558	ZNF83	Zinc finger protein-83	ZNF83	55769	ENSG00000167766						
chr19	52838531	52857648	19q13.4	19q13.41		616841	ZNF468	Zinc finger protein 468	ZNF468	90333	ENSG00000204604						
chr19	52859490	52897726	19q13.3-q13.4	19q13.41		606427	ZNF320	Zinc finger protein 320	ZNF320	162967	ENSG00000204604						
chr19	53066613	53103433	19q13.3-q13.4	19q13.41-q13.42		600398	ZNF160	Zinc finger protein-160	ZNF160	90338	ENSG00000170949						
chr19	53503818	53580268	19q13.3-q13.4	19q13.42		606043	"ZNF331, ZNF463"	Zinc finger protein-331	ZNF331	55422	ENSG00000130844						
chr19	53601113	53637056	19q13.42	19q13.42		611165	DPRX	Divergent-paired related homeobox	DPRX	503834	ENSG00000204595	many pseudogenes					
chr19	53707452	53707538	19q13.42	19q13.42		615908	MIR520C	Micro RNA 520C	MIR520C	574476							
chr19	53713346	53713433	19q13.42	19q13.42		614247	"MIR519D, MIRN519D"	Micro RNA 519D	MIR519D	574480							
chr19	53722165	53722254	19q13.42	19q13.42		616272	MIR520G	Micro RNA 520G	MIR520G	574484							
chr19	53742511	53742598	19q13.42	19q13.42		614755	MIR520H	Micro RNA 520H	MIR520H	574493							
chr19	53787674	53787740	19q13.41	19q13.42		612043	MIR371A	Micro RNA 371A	MIR371A	442916							
chr19	53787889	53787955	19q13.41	19q13.42		612044	"MIR372, MIRN372"	Micro RNA 372	MIR372	442917							
chr19	53788704	53788772	19q13.41	19q13.42		611954	"MIR373, MIRN373"	Micro RNA 373	MIR373	442918							
chr19	53793583	53824402	19q13.4	19q13.42		609648	"NLRP12, NALP12, PYPAF7, RNO, FCAS2"	"NLR family, pyrin domain containing 12"	NLRP12	91662	ENSG00000142405		"Familial cold autoinflammatory syndrome 2, 611762 (3), Autosomal dominant"	Nlrp12 (MGI:2676630)			
chr19	53865583	53876434	19q13.33-q13.4	19q13.42		609959	MYADM	Myeloid-associated differentiation marker	MYADM	91663	ENSG00000179820			Myadm (MGI:1355332)			
chr19	53882183	53907646	19q13.4	19q13.42		176980	"PRKCG, PKCC, PKCG, SCA14"	"Protein kinase C, gamma polypeptide"	PRKCG	5582	ENSG00000126583		"Spinocerebellar ataxia 14, 605361 (3), Autosomal dominant"	Prkcg (MGI:97597)			
chr19	53909424	53943943	19q13.4	19q13.42		606899	CACNG7	"Calcium channel, voltage-dependent, gamma-7 subunit"	CACNG7	59284	ENSG00000105605			Cacng7 (MGI:1932374)			
chr19	53963035	53990214	19q13.4	19q13.42		606900	CACNG8	"Calcium channel, voltage-dependent, gamma-8 subunit"	CACNG8	59283	ENSG00000142408			Cacng8 (MGI:1932376)			
chr19	53991148	54012665	19q13.4	19q13.42		606898	CACNG6	"Calcium channel, voltage-dependent, gamma-6 subunit"	CACNG6	59285	ENSG00000130433			Cacng6 (MGI:1859168)			
chr19	54040824	54063965	19q13.4	19q13.42		616804	"VSTM1, SIRL1"	V-SET and transmembrane domains-containing protein 1	VSTM1	284415	ENSG00000189068						
chr19	54069894	54081364	19q13.4	19q13.42		616802	TARM1	T cell-interacting activating receptor on myeloid cells 1	TARM1	441864	ENSG00000248385			Tarm1 (MGI:2442280)			
chr19	54094667	54102685	19q13.4	19q13.42		606862	OSCAR	Osteoclast-associated receptor	OSCAR	126014	ENSG00000170909			Oscar (MGI:2179720)			
chr19	54102337	54106973	19q13.42	19q13.42		603832	NDUFA3	"NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 3"	NDUFA3	4696	ENSG00000170906			Ndufa3 (MGI:1913341)			
chr19	54115409	54131718	19q13.4	19q13.42		606419	"PRPF31, PRP31, RP11"	"Precursor RNA-processing factor 31, S. cerevisiae, homolog of"	PRPF31	26121	ENSG00000105618		"Retinitis pigmentosa 11, 600138 (3), Autosomal dominant"	Prpf31 (MGI:1916238)			
chr19	54137688	54155707	19q13.4	19q13.42		604910	"CNOT3, NOT3"	"CCR4-NOT transcription complex, subunit 3"	CNOT3	4849	ENSG00000088038			Cnot3 (MGI:2385261)			
chr19	54160094	54173249	19q13.42	19q13.42		617181	TMC4	Transmembrane channel-like protein 4	TMC4	147798	ENSG00000167608			Tmc4 (MGI:2669035)			
chr19	54173411	54189881	19q13.4	19q13.42		606048	"MBOAT7, BB1, LENG4, MRT57"	Membrane bound O-acyltransferase domain containing 7	MBOAT7	79143	ENSG00000125505		"Mental retardation, autosomal recessive 57, 617188 (3), Autosomal recessive"	Mboat7 (MGI:1924832)			
chr19	54189969	54194535	19q13.4	19q13.42		608754	"TSEN34, PCH2C, LENG5, SEN34"	"tRNA splicing endonuclease 34, S. cerevisiae, homolog of"	TSEN34	79042	ENSG00000170892	mutation identified in 1 PCH2C patient	"?Pontocerebellar hypoplasia type 2C, 612390 (3)"	Tsen34 (MGI:1913328)			
chr19	54200556	54207646	19q13.4	19q13.42		603631	RPS9	Ribosomal protein S9	RPS9	6203	ENSG00000170889			Rps9 (MGI:1924096)			
chr19	54216277	54223086	19q13.4	19q13.42		604820	"LILRB3, LIR3, ILT5, HL9"	"Leukocyte immunoglobulin-like receptor, subfamily B, member 3"	LILRB3	11025	ENSG00000204577			"Pira1,Lilra6,Pira2,Gm14548,Pira6,Gm15448,Pirb (MGI:1195970,MGI:1195974,MGI:3705216,MGI:1195971,MGI:894311,MGI:3709645,MGI:1195969)"			
chr19	54250404	54257307	19q13.2	19q13.42		604814	"LILRB5, LIR8"	"Leukocyte immunoglobulin-like receptor, subfamily B, member 5"	LILRB5	10990	ENSG00000105609						
chr19	54273820	54281177	19q13.4	19q13.42		604815	"LILRB2, LIR2, ILT4, MIR10"	"Leukocyte immunoglobulin-like receptor, subfamily B, member 2"	LILRB2	10288	ENSG00000131042						
chr19	54307069	54313138	19q13.4	19q13.42		606047	"LILRA9, ILT11, CD85F, LIR9"	"Leukocyte immunoglobulin-like receptor, subfamily A, member 5"	LILRA5	353514	ENSG00000187116			Lilra5 (MGI:3647196)			
chr19	54333184	54339168	19q13.42	19q13.42		607517	"LILRA4, ILT7"	"Leukocyte immunoglobulin-like receptor, subfamily A, member 4"	LILRA4	23547	ENSG00000239961						
chr19	54353623	54370555	19q13.4	19q13.42		602992	LAIR1	Leukocyte-associated immunoglobulin-like receptor 1	LAIR1	3903	ENSG00000167613			Lair1 (MGI:105492)			
chr19	54415430	54436718	19q13.4	19q13.42		605784	TTYH1	"Tweety, Drosophila, homolog of, 1"	TTYH1	57348	ENSG00000167614			Ttyh1 (MGI:1889007)			
chr19	54447620	54462045	19q13.42	19q13.42		616575	"LENG8, KIAA1932"	Leukocyte receptor cluster gene 8	LENG8	114823	ENSG00000167615			Leng8 (MGI:2142195)			
chr19	54465024	54473289	19q13.42	19q13.42		609171	"CDC42EP5, CEP5, BORG3"	CDC42 effector protein 5	CDC42EP5	148170	ENSG00000167617			Cdc42ep5 (MGI:1929745)			
chr19	54502796	54510692	19q13.42	19q13.42		602993	"LIAR2, CD306"	Leukocyte-associated immunoglobulin-like receptor 2	LAIR2	3904	ENSG00000167618						
chr19	54572996	54587559	19q13.4	19q13.42		604812	"LILRA2, LIR7, ILT1"	"Leukocyte immunoglobulin-like receptor, subfamily A, member 2"	LILRA2	11027	ENSG00000239998						
chr19	54593575	54602380	19q13.2	19q13.42		604810	"LILRA1, LIR6"	"Leukocyte immunoglobulin-like receptor, subfamily A, member 1"	LILRA1	11024	ENSG00000104974						
chr19	54616929	54637924	19q13.4	19q13.42		604811	"LILRB1, LIR1, ILT2, MIR7, CD85"	"Leukocyte immunoglobulin-like receptor, subfamily B, member 1"	LILRB1	10859	ENSG00000104972						
chr19	54662523	54670358	19q13.4	19q13.42		604821	"LILRB4, LIR5, ILT3, HM18"	"Leukocyte immunoglobulin-like receptor, subfamily B, member 4"	LILRB4	11006	ENSG00000186818			"Lilrb4a,Lilr4b (MGI:102701,MGI:102702)"			
chr19	54724446	54736535	19q13.4	19q13.42		610095	"KIR3KL3, KIRC1, KIR3DL7, KIR44"	"Killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3"	KIR3DL3	115653	ENSG00000242019			"Kir3dl2,Kir3dl1 (MGI:2652397,MGI:3612791)"			
chr19	54738508	54753051	19q13.4	19q13.42		604938	"KIR2DL3, NKAT2"	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3"	KIR2DL3	3804	ENSG00000243772						
chr19	54769207	54784325	19q13.4	19q13.42		604936	"KIR2DL1, NKAT1"	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1"	KIR2DL1	3802	ENSG00000125498						
chr19	54786361	54790417	19q13.4	19q13.42		610604	"KIR3DP1, CD158C, KIRX, KIR48, KIR2DS6"	"Killer cell immunoglobulin-like receptor, three domains, pseudogene"	KIR3DP1	548594		functional in some individuals					
chr19	54803611	54814516	19q13.4	19q13.42		604945	"KIR2DL4, KIR103AS"	"Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4"	KIR2DL4	3805	ENSG00000189013						
chr19	54816437	54830777	19q13.4	19q13.42		604946	"KIR3DL1, NKAT3, NKB1, AMB11, KIR3DS1"	"Killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1"	KIR3DL1	3811	ENSG00000167633		"{AIDS, delayed/rapid progression to}, 609423 (3)"				
chr19	54832675	54848568	19q13.4	19q13.42		604955	"KIR2DS4, NKAT8"	"Killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 4"	KIR2DS4	3809	ENSG00000221957						
chr19	54850319	54867214	19q13.4	19q13.42		604947	"KIR3DL2, NKAT4"	"Killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2"	KIR3DL2	3812	ENSG00000240403						
chr19	54874092	54891419	19q13.4	19q13.42		147045	FCAR	"Fc fragment of IgA, receptor for"	FCAR	2204	ENSG00000186431						
chr19	54906062	54938210	19q13.42	19q13.42		604530	"NCR1, LY94, NKP46"	"Natural cytotoxicity triggering receptor 1 (lymphocyte antigen 94, mouse, homolog of)"	NCR1	9437	ENSG00000189430			Ncr1 (MGI:1336212)			
chr19	54923508	54965183	19q13.4	19q13.42		609661	"NALP7, NOD12, PYPAF3, HYDM"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 7"	NLRP7	199713	ENSG00000167634		"Hydatidiform mole, recurrent, 1, 231090 (3), Autosomal recessive"				
chr19	54965278	55001141	19q13.4	19q13.42		609364	"NALP2, PAN1, PYPAF2"	"NACHT-, leucine-rich repeat-, and PYD-containing 2"	NLRP2	55655	ENSG00000022556			Nlrp2 (MGI:3041206)			
chr19	55013704	55038263	19q13.4	19q13.42		605546	"GP6, GPIV, BDPLT11"	"Glycoprotein VI, platelet"	GP6	51206	ENSG00000088053		"Bleeding disorder, platelet-type, 11, 614201 (3), Autosomal recessive"	Gp6 (MGI:1889810)			
chr19	55075852	55087922	19q13.4	19q13.42		614987	"EPS8L1, EPS8R1"	EPS8-like protein 1	EPS8L1	54869	ENSG00000131037			Eps8l1 (MGI:1914675)			
chr19	55090912	55117599	19q13.3-q13.4	19q13.42		613245	"PPP1R12C, MBS85"	"Protein phosphatase 1, regulatory subunit 12C"	PPP1R12C	54776	ENSG00000125503			Ppp1r12c (MGI:1924258)			
chr19	55132697	55149353	19q13.4	19q13.42		191041	"TNNT1, ANM, NEM5"	"Troponin-T1, skeletal, slow"	TNNT1	7138	ENSG00000105048		"Nemaline myopathy 5, Amish type, 605355 (3), Autosomal recessive"	Tnnt1 (MGI:1333868)			
chr19	55151766	55157731	19q13.4	19q13.42		191044	"TNNI3, CMH7, CMD2A, RCM1, CMD1FF"	"Troponin-I, cardiac"	TNNI3	7137	ENSG00000129991	mutation identified in 1 CMD2A family	"Cardiomyopathy, dilated, 1FF, 613286 (3); ?Cardiomyopathy, dilated, 2A, 611880 (3), Autosomal recessive; Cardiomyopathy, familial restrictive, 1, 115210 (3), Autosomal dominant; Cardiomyopathy, hypertrophic, 7, 613690 (3), Autosomal dominant"	Tnni3 (MGI:98783)			
chr19	55158660	55166721	19q13.4	19q13.42		614566	"DNAAF3, PF22, DAB1, CILD2"	"Dynein, axonemal, assembly factor 3"	DNAAF3	352909	ENSG00000167646		"Ciliary dyskinesia, primary, 2, 606763 (3), Autosomal recessive"	Dnaaf3 (MGI:3588207)			
chr19	55173094	55180440	19q13.42	19q13.42		600782	SYT5	Synaptotagmin-5	SYT5	6861	ENSG00000129990			Syt5 (MGI:1926368)			
chr19	55181246	55209505	19q13.4	19q13.42		602510	PTPRH	"Protein tyrosine phosphatase, receptor type, H"	PTPRH	5794	ENSG00000080031			Ptprh (MGI:3026877)			
chr19	55226633	55229263	19q13.42	19q13.42		617806	TMEM86B	Transmembrane protein 86B	TMEM86B	255043	ENSG00000180089			Tmem86b (MGI:1915505)			
chr19	55229778	55258669	19q13.42	19q13.42		610875	"SAPS1, PP6R1, KIAA1115"	"SAPS domain family, member 1"	PPP6R1	22870	ENSG00000105063			Ppp6r1 (MGI:2442163)			
chr19	55262221	55280422	19q13.42	19q13.42		612939	HSPBP1	Heat-shock 70kD protein-binding protein 1	HSPBP1	23640	ENSG00000133265			Hspbp1 (MGI:1913495)			
chr19	55284100	55312561	19q13.4	19q13.42		609235	"BRSK1, KIAA1811"	BR serine/threonine kinase 1	BRSK1	84446	ENSG00000160469			Brsk1 (MGI:2685946)			
chr19	55308868	55334042	19q13.42	19q13.42		617291	"TMEM150B, DRAM3, TTN2, TMEM224"	Transmembrane protein 150B	TMEM150B	284417	ENSG00000180061			Tmem150b (MGI:2679718)			
chr19	55339852	55348120	19q13.42	19q13.42		613198	SUV420H2	"Suppressor of variegation 4-20, Drosophila, homolog of, 2"	KMT5C	84787	ENSG00000133247			Kmt5c (MGI:2385262)			
chr19	55364381	55370462	19q13.3-q13.4	19q13.42		147681	IL11	Interleukin-11	IL11	3589	ENSG00000095752			Il11 (MGI:107613)			
chr19	55385931	55403247	19q13.4	19q13.42		603638	RPL28	Ribosomal protein L28	RPL28	6158	ENSG00000108107			Rpl28 (MGI:101839)			
chr19	55401281	55408438	19q13.42	19q13.42		610309	"UBE2S, EPF5, E2EPF"	Ubiquitin-conjugating enzyme E2S	UBE2S	27338	ENSG00000108106			Ube2s (MGI:1925141)			
chr19	55428737	55442862	19q13.42	19q13.42		617328	SHISA7	"Shisa family, member 7"	SHISA7	729956	ENSG00000187902			Shisa7 (MGI:3605641)			
chr19	55452977	55461681	19q13.42	19q13.42		612928	ISOC2	Isochorismatase domain-containing 2	ISOC2	79763	ENSG00000063241			Isoc2a (MGI:3609243)			
chr19	55476331	55484486	19q13.4	19q13.42		610671	"ZNF628, ZEC"	Zinc finger protein 628	ZNF628	89887	ENSG00000197483			Zfp628 (MGI:2665174)			
chr19	55591370	55599702	19q13.42	19q13.42		609133	"FIZ1, FLJ14768"	FLT3-interacting zinc finger protein 1	FIZ1	84922	ENSG00000179943			Fiz1 (MGI:1344336)			
chr19	55641025	55643469	19q13.42	19q13.42		617888	ZNF580	Zinc finger protein 580	ZNF580	51157	ENSG00000213015			Zfp580 (MGI:1916242)			
chr19	55647392	55653160	19q13.42	19q13.42		613478	CCDC106	Coiled-coil domain-containing protein 106	CCDC106	29903	ENSG00000173581			Ccdc106 (MGI:2385900)			
chr19	55654049	55674715	19q13.42	19q13.42		191318	"U2AF2, U2AF65"	U2 small nuclear RNA auxiliary factor 2	U2AF2	11338	ENSG00000063244			U2af2 (MGI:98886)			
chr19	55675194	55695766	19q13	19q13.42		607262	EPN1	Epsin 1	EPN1	29924	ENSG00000063245			Epn1 (MGI:1333763)			
chr19	55708431	55738401	19q13.4	19q13.42		609663	"NALP9, NOD6"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 9"	NLRP9	338321	ENSG00000185792			Nlrp9b (MGI:2675377)			
chr19	55757297	55763420	19q13.4	19q13.42		612601	"RFPL4A, RNF210"	Ret finger protein-like 4A	RFPL4A	342931	ENSG00000223638						
chr19	55785396	55836761	19q13.4	19q13.42-q13.43		609664	"NALP11, PYPAF7, NOD17"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 11"	NLRP11	204801	ENSG00000179873						
chr19	55836577	55881854	19q13.4	19q13.43		609645	"NALP4, PAN2, PYPAF4"	"NACHT domain-, leucine-rich repeat-c and PYD-containing protein 4"	NLRP4	147945	ENSG00000160505			"Nlrp4c,Nlrp4e (MGI:3056600,MGI:1890518)"			
chr19	55891691	55932335	19q13.4	19q13.43		609660	"NALP13, NOD14"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 13"	NLRP13	126204	ENSG00000173572						
chr19	55947831	55988628	19q13.4	19q13.43		609659	"NALP8, NOD16, PAN4"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 8"	NLRP8	126205	ENSG00000179709						
chr19	55999725	56061809	19q13	19q13.43		609658	"NALP5, MATER"	"NACHT domain-, leucine-rich repeat-, and PYD-containing protein 5"	NLRP5	126206	ENSG00000171487			Nlrp5 (MGI:1345193)			
chr19	56132508	56160892	19q13.43	19q13.43		607874	"ZNF444, EZF2"	Zinc finger protein 444	ZNF444	55311	ENSG00000167685			Zfp444 (MGI:1923365)			
chr19	56176019	56185774	19q13.4	19q13.43		611178	"GALP, ALARIN"	Galanin-like peptide (GALP precursor protein)	GALP	85569	ENSG00000197487			Galp (MGI:2663979)			
chr19	56382750	56393600	19q13.43	19q13.43		615600	ZNF582	Zinc finger protein 582	ZNF582	147948	ENSG00000018869						
chr19	56438511	56478064	19q13.4	19q13.43		611024	"ZNF667, MIPU1"	Zinc finger protein 667	ZNF667	63934	ENSG00000198046			Zfp667 (MGI:2442757)			
chr19	56536789	56559191	19q13.4	19q13.43		616798	ZFP28	Zinc finger protein 28	ZFP28	140612	ENSG00000196867			Zfp28 (MGI:99175)			
chr19	56595258	56624480	19q13.4	19q13.43		194545	ZNF71	Zinc finger protein-71 (Cos26)	ZNF71	58491	ENSG00000197951	previously assigned to 22q11.2					
chr19	56810076	56840725	19q13.4	19q13.43		601483	PEG3	Paternally expressed gene 3	PEG3	5178	ENSG00000198300			Peg3 (MGI:104748)			
chr19	57151725	57167487	19q13.43	19q13.43		611168	DUXA	Double homeobox A	DUXA	503835	ENSG00000258873	many pseudogenes					
chr19	57191499	57222845	19q13.4	19q13.43		604668	ZNF264	Zinc finger protein-264	ZNF264	9422	ENSG00000083844						
chr19	57230316	57235549	19q13.43	19q13.43		603495	"AURKC, STK13, AIE2, SPGF5"	Aurora kinase C	AURKC	6795	ENSG00000105146		"Spermatogenic failure 5, 243060 (3), Autosomal recessive"	Aurkc (MGI:1321119)			
chr19	57279966	57294067	19q13.4	19q13.43		604755	"ZNF272, HZF8, ZNF460"	Zinc finger protein-272	ZNF460	10794	ENSG00000197714						
chr19	57320496	57330775	19q13.43	19q13.43		616847	ZNF543	Zinc finger protein 543	ZNF543	125919	ENSG00000178229						
chr19	57351252	57359897	19q13.43	19q13.43		613840	ZNF304	Zinc finger protein 304	ZNF304	57343	ENSG00000131845						
chr19	57455173	57456738	19q13.4	19q13.43		605234	"VN1R1, V1RL1"	Vomeronasal 1 receptor 1	VN1R1	57191	ENSG00000178201						
chr19	57487710	57494679	19q13.43	19q13.43		617410	ZNF419	Zinc finger protein 419	ZNF419	79744	ENSG00000105136						
chr19	57614218	57624716	19q13.4	19q13.43		604076	ZNF134	Zinc finger protein-134	ZNF134	7693	ENSG00000213762						
chr19	57633166	57644045	19q13.4	19q13.43		601856	ZNFC25	Zinc finger protein-C2H2-25	ZNF211	10520	ENSG00000121417						
chr19	57651496	57679151	19q13.43	19q13.43		613419	"ZSCAN4, ZNF494"	Zinc finger- and SCAN domain-containing protein 4	ZSCAN4	201516	ENSG00000180532						
chr19	57696274	57709210	19q13.4	19q13.43		604085	ZNF154	Zinc finger protein-154	ZNF154	7710	ENSG00000179909						
chr19	57940832	57947708	19q13	19q13.43		606956	ZNF256	Zinc finger protein 256	ZNF256	10172	ENSG00000152454						
chr19	57977052	58003345	19q13.4	19q13.43		613905	"ZNF606, ZNF328, KIAA1852"	Zinc finger protein 606	ZNF606	80095	ENSG00000166704			Zfp606 (MGI:1914620)			
chr19	58059226	58069754	19q13.4	19q13.43		604077	ZNF135	Zinc finger protein-135	ZNF135	7694	ENSG00000176293						
chr19	58182988	58213561	19q13.4	19q13.43		605467	ZNF274	Zinc finger protein-274	ZNF274	10782	ENSG00000171606			"Zfp369,Zfp110 (MGI:1890378,MGI:2176229)"			
chr19	58278951	58295887	19q13.43	19q13.43		194532	ZNF8	Zinc finger protein-8	ZNF8	7554	ENSG00000278129	previously assigned to 20q13		Zfp128 (MGI:2389445)			
chr19	58326999	58342345	19q13.43	19q13.43		165260	"ZSCAN22, HKR2"	Zinc finger- and SCAN domain-containing protein 22	ZSCAN22	342945	ENSG00000182318			Zscan22 (MGI:2443312)			
chr19	58346805	58353498	19cen-q13.2	19q13.43		138670	A1BG	"Glycoprotein, alpha-1B"	A1BG	1	ENSG00000121410	order:  C3-SE-LU-A1BG		A1bg (MGI:2152878)			
chr19	58387268	58394803	19q13.4	19q13.43		603630	RPS5	Ribosomal protein S5	RPS5	6193	ENSG00000083845			Rps5 (MGI:1097682)			
chr19	58432813	58440221	19q13.4	19q13.43		604074	ZNF132	Zinc finger protein-132	ZNF132	7691	ENSG00000131849						
chr19	58467044	58473577	19q13.43	19q13.43		617477	"ZNF324, ZF5128"	Zinc finger protein 324	ZNF324	25799	ENSG00000083812			Zfp324 (MGI:2444641)			
chr19	58498332	58512064	19q13.43	19q13.43		603314	"SLC27A5, FATP5, VLACSR, VLCSH2"	"Solute carrier family 27 (fatty acid transporter), member 5"	SLC27A5	10998	ENSG00000083807			Slc27a5 (MGI:1347100)			
chr19	58544468	58550721	19q13.4	19q13.43		601742	"TRIM28, KAP1, TIF1B"	Tripartite motif-containing protein 28	TRIM28	10155	ENSG00000130726			Trim28 (MGI:109274)			
chr19	58551565	58555623	19q	19q13.43		610893	"CHMP2A, VPS2A, VPS2, BC2"	"CHMP family, member 2A"	CHMP2A	27243	ENSG00000130724			Chmp2a (MGI:1916203)			
chr19	58555711	58558975	19q13.43	19q13.43		603173	"UBE2M, UBC12"	Ubiquitin-conjugating enzyme E2M	UBE2M	9040	ENSG00000130725			Ube2m (MGI:108278)			
chr19	58561916	58574477	19q13.2-q13.4	19q13.43		194550	"ZNF42, MZF1"	Zinc finger protein-42 (myeloid-specific retinoic acid responsive)	MZF1	7593	ENSG00000099326			Mzf1 (MGI:107457)			
chr19	0	58617616	Chr.19			603979	ZNF97	Zinc finger protein-97									
chr20	0	28100000	20p			607116	AD8	Alzheimer disease 8		353128		?related to CST3	"Alzheimer disease 8, 607116 (2)"				
chr20	0	5100000	20p13			608031	ALS7	Amyotrophic lateral sclerosis 7	ALS7	406238		max lod at D20S103	"Amyotrophic lateral sclerosis 7, 608031 (2)"				
chr20	0	28100000	20p			605804	ATOD3	"Dermatitis, atopic, 3"		117187		max lod at D20S115	"{Dermatitis, atopic, susceptibility to, 3}, 605804 (2)"				
chr20	0	25700000	20pter-p11.2			608559	BMIQ6	Body mass index quantitative trait locus 6	BMIQ6	449017		near D20S482 and D20S851	"[Body mass index QTL6], 608559 (2)"				
chr20	0	5100000	20p13			611242	RLS5	"Restless legs syndrome, susceptibility to, 5"		100188839		max lod at D20S849	"{Restless legs syndrome 5}, 611242 (2)"				
chr20	325570	330227	20p13	20p13		601947	"SOX12, SOX22"	SRY (sex-determining region Y)-box 12	SOX12	6666	ENSG00000177732			Sox12 (MGI:98360)			
chr20	346725	359704	20p13	20p13		610666	NRSN2	Neurensin 2	NRSN2	80023	ENSG00000125841			Nrsn2 (MGI:2684969)			
chr20	380628	397558	20p13	20p13		607898	"TRIB3, NIPK, SINK, C20orf97, SKIP3"	"Tribbles, Drosophila, homolog of, 3"	TRIB3	57761	ENSG00000101255			Trib3 (MGI:1345675)			
chr20	408049	432138	20p13	20p13		610924	"RBCK1, HOIL1, PGBM1, PBMEI"	RANBP-type and C3HC4-type zinc finger-containing 1	RBCK1	10616	ENSG00000125826		"Polyglucosan body myopathy 1 with or without immunodeficiency, 615895 (3), Autosomal recessive"	Rbck1 (MGI:1344372)			
chr20	435476	462552	20p13	20p13		611663	"TBC1D20, C20orf140, WARBM4"	"TBC1 domain family, member 20"	TBC1D20	128637	ENSG00000125875		"Warburg micro syndrome 4, 615663 (3), Autosomal recessive"	Tbc1d20 (MGI:1914481)			
chr20	472497	543837	20p13	20p13		115440	"CSNK2A1, CK2A1, OCNDS"	"Casein kinase-2, alpha-1 polypeptide"	CSNK2A1	1457	ENSG00000101266	pseudogene on 11p15	"Okur-Chung neurodevelopmental syndrome, 617062 (3), Autosomal dominant"	Csnk2a1 (MGI:88543)			
chr20	603992	610265	20p13	20p13		601010	TCF15	Transcription factor-15 (basic helix-loop-helix)	TCF15	6939	ENSG00000125878			Tcf15 (MGI:104664)			
chr20	646614	653369	20p13	20p13		617583	"SRXN1, SRX"	Sulfiredoxin 1	SRXN1	140809	ENSG00000271303			Srxn1 (MGI:104971)			
chr20	760079	776014	20p13	20p13		613350	"SLC52A3, C20orf54, RFT2, BVVLS1"	"Solute carrier family 52, riboflavin transporter, member 3"	SLC52A3	113278	ENSG00000101276	mutation identified in 1 FZLD family	"Brown-Vialetto-Van Laere syndrome 1, 211530 (3), Autosomal recessive; ?Fazio-Londe disease, 211500 (3), Autosomal recessive"	Slc52a3 (MGI:1916948)			
chr20	833696	846278	20p13	20p13		611393	"FAM110A, C20orf55"	"Family with sequence similarity 110, member A"	FAM110A	83541	ENSG00000125898			Fam110a (MGI:1921097)			
chr20	869898	916367	20p13	20p13		603705	"ANGPT4, ANG4"	Angiopoietin 4	ANGPT4	51378	ENSG00000101280	no ANGT3 in human		Angpt4 (MGI:1336887)			
chr20	958451	1002263	20p13	20p13		610573	"RSPO4, CRISTIN4"	"R-spondin family, member 4"	RSPO4	343637	ENSG00000101282		"Anonychia congenita, 206800 (3), Autosomal recessive"	Rspo4 (MGI:1924467)			
chr20	1113228	1172245	20p13	20p13		617858	"PSMF1, PI31"	Proteasome inhibitor subunit 1	PSMF1	9491	ENSG00000125818			Psmf1 (MGI:1346072)			
chr20	1266290	1309326	20p13	20p13		604942	SNPH	Syntaphilin	SNPH	9751	ENSG00000101298			Snph (MGI:2139270)			
chr20	1309908	1329234	20p13	20p13		617358	"SDCBP2, SITAC, ST2, SITAC18"	Syndecan-binding protein 2	SDCBP2	27111	ENSG00000125775			Sdcbp2 (MGI:2385156)			
chr20	1368976	1393171	20p13	20p13		186945	"FKBP1A, FKBP12"	"FK506-binding protein-1A, 12kD"	FKBP1A	2280	ENSG00000088832			Fkbp1a (MGI:95541)			
chr20	1442161	1467792	20p	20p13		606610	P47	"p47, rat, homolog of"	NSFL1C	55968	ENSG00000088833			Nsfl1c (MGI:3042273)			
chr20	1629151	1686515	20p13	20p13		605466	"SIRPG, SIRPB2"	"Signal regulatory protein, gamma"	SIRPG	55423	ENSG00000089012						
chr20	1894166	1939894	20p13	20p13		602461	SHPS1	SHP substrate-1	SIRPA	140885	ENSG00000198053			Sirpa (MGI:108563)			
chr20	1978755	1994284	20p13	20p13		131340	"PDYN, SCA23"	Prodynorphin	PDYN	5173	ENSG00000101327		"Spinocerebellar ataxia 23, 610245 (3), Autosomal dominant"	Pdyn (MGI:97535)			
chr20	2098020	2148554	20p13	20p13		609370	"STK35, CLIK1"	Serine/threonine kinase 35	STK35	140901	ENSG00000125834			Stk35 (MGI:1914583)			
chr20	2295966	2341078	20q12	20p13		600238	"TGM3, UHS2"	"Transglutaminase-3 (E polypeptide, protein-glutamine-gamma-glutamyl transferase)"	TGM3	7053	ENSG00000125780	mutation identified in 1 UHS2 patient	"?Uncombable hair syndrome 2, 617251 (3), Autosomal recessive"	Tgm3 (MGI:98732)			
chr20	2380907	2432752	20p13-p12.2	20p13		613900	"TGM6, TG6, TGY, SCA35"	Transglutaminase 6	TGM6	343641	ENSG00000166948		"Spinocerebellar ataxia 35, 613908 (3), Autosomal dominant"	Tgm6 (MGI:3044321)			
chr20	2461634	2470852	20p13	20p13		182282	"SNRPB, CCMS"	Small nuclear ribonucleoprotein polypeptides B and B1	SNRPB	6628	ENSG00000125835		"Cerebrocostomandibular syndrome, 117650 (3), Autosomal dominant"	Snrpb (MGI:98342)			
chr20	2536606	2641783	20p13	20p13		606707	TMC2	Transmembrane channel-like protein 2	TMC2	117532	ENSG00000149488			Tmc2 (MGI:2151017)			
chr20	2652531	2658392	20p13	20p13		614154	"NOP56, SCA36"	"Nop56, S. cerevisiae, homolog of"	NOP56	10528	ENSG00000101361		"Spinocerebellar ataxia 36, 614153 (3), Autosomal dominant"	Nop56 (MGI:1914384)			
chr20	2652776	2652841	20p13	20p13		614155	"MIR1292, MIRN1292"	Micro RNA 1292	MIR1292	100302138							
chr20	2658389	2664222	20p13	20p13		604526	"IDH3B, RP46"	"Isocitrate dehydrogenase 3, beta subunit"	IDH3B	3420	ENSG00000101365		"Retinitis pigmentosa 46, 612572 (3)"	Idh3b (MGI:2158650)			
chr20	2692877	2760107	20p13	20p13		609935	"EBF4, KIAA1442"	Early B-cell factor 4	EBF4	57593	ENSG00000088881			Ebf4 (MGI:2385972)			
chr20	2840696	2866731	20p13	20p13		608550	VPS16	"Vacuolar protein sorting 18, yeast, homolog of"	VPS16	64601	ENSG00000215305			Vps16 (MGI:2136772)			
chr20	2864194	3038668	20p13	20p13		176884	"PTPRA, PTPA, PTPRL2, LRP"	"Protein tyrosine phosphatase, receptor type, alpha polypeptide"	PTPRA	5786	ENSG00000132670			Ptpra (MGI:97808)			
chr20	3039060	3045895	20p13	20p13		602352	GNRH2	Gonadotropin-releasing hormone-2	GNRH2	2797	ENSG00000125787						
chr20	3046028	3048249	20p13	20p13		611988	"MRPS26, MRPS13"	Mitochondrial ribosomal protein S26	MRPS26	64949	ENSG00000125901			Mrps26 (MGI:1333830)			
chr20	3068870	3072516	20p13	20p13		167050	OXT	Oxytocin-neurophysin I	OXT	5020	ENSG00000101405	12kb from ARVP		Oxt (MGI:97453)			
chr20	3082555	3093520	20p13	20p13		192340	"AVP, AVRP, VP"	"Arginine vasopressin (neurophysin II, antidiuretic hormone)"	AVP	551	ENSG00000101200	distal 20p	"Diabetes insipidus, neurohypophyseal, 125700 (3), Autosomal dominant"	Avp (MGI:88121)			
chr20	3146518	3159885	20p13	20p13		614272	FASTKD5	Fast kinase domain-containing protein 5	FASTKD5	60493	ENSG00000215251			Fastkd5 (MGI:2139469)			
chr20	3162616	3173596	20p13	20p13		610484	"PROSAPIP1, KIAA0552"	Proline-rich synapse-associated protein-interacting protein 1	LZTS3	9762	ENSG00000088899			Lzts3 (MGI:2656976)			
chr20	3190349	3204696	20p13	20p13		616177	"DDRGK1, UFBP1, C20orf116, SEMDSH"	DDRGK domain-containing protein 1	DDRGK1	65992	ENSG00000198171		"Spondyloepimetaphyseal dysplasia, Shohat type, 602557 (3), Autosomal recessive"	Ddrgk1 (MGI:1924256)			
chr20	3208867	3227448	20p	20p13		147520	"ITPA, EIEE35"	Inosine triphosphatase-A	ITPA	3704	ENSG00000125877		"Epileptic encephalopathy, early infantile, 35, 616647 (3), Autosomal recessive; [Inosine triphosphatase deficiency], 613850 (3)"	Itpa (MGI:96622)			
chr20	3227416	3241483	20p13-p12	20p13		610206	"SLC4A11, BTR1, NABC1, CHED, CDPD, FECD4"	"Solute carrier family 4 (sodium borate cotransporter), member 11"	SLC4A11	83959	ENSG00000088836		"Corneal dystrophy, Fuchs endothelial, 4, 613268 (3); Corneal endothelial dystrophy and perceptive deafness, 217400 (3), Autosomal recessive; Corneal endothelial dystrophy, autosomal recessive, 217700 (3), Autosomal recessive"	Slc4a11 (MGI:2138987)			
chr20	3249301	3407661	20p13	20p13		614146	C20orf194	Chromosome 20 open reading frame 194	C20orf194	25943	ENSG00000088854			4930402H24Rik (MGI:1923029)			
chr20	3471017	3651121	20p13	20p13		603130	"ATRN, MGCA"	"Attractin (mahogany, mouse, homolog of)"	ATRN	8455	ENSG00000088812			Atrn (MGI:1341628)			
chr20	3667964	3682689	20p13	20p13		607114	ADAM33	A disintegrin and metalloproteinase domain 33	ADAM33	80332	ENSG00000149451			Adam33 (MGI:1341813)			
chr20	3686969	3712557	20p13	20p13		600751	"SIGLEC1, SN, CD169"	Sialic acid-binding immunoglobulin-like lectin 1 (sialoadhesin)	SIGLEC1	6614	ENSG00000088827			Siglec1 (MGI:99668)			
chr20	3732669	3753110	20p13	20p13		610702	HSPA12B	Heat-shock 70kD protein 12B	HSPA12B	116835	ENSG00000132622			Hspa12b (MGI:1919880)			
chr20	3777503	3781465	20p13	20p13		610674	"C20orf28, CLAMP, SPEF1"	Sperm flagellar protein 1	SPEF1	25876	ENSG00000101222			Spef1 (MGI:3513546)			
chr20	3783850	3786689	20p13	20p13		117140	CENPB	Centromeric protein B	CENPB	1059	ENSG00000125817			Cenpb (MGI:88376)			
chr20	3786771	3806120	20p13	20p13		116949	CDC25B	Cell division cycle 25B	CDC25B	994	ENSG00000101224			Cdc25b (MGI:99701)			
chr20	3820523	3825306	20p13	20p13		614824	"AP5S1, C20orf29"	"Adaptor-related protein complex 5, sigma-1 subunit"	AP5S1	55317	ENSG00000125843			Ap5s1 (MGI:1916846)			
chr20	3846798	3876122	20p13	20p13		609676	"MAVS, VISA, IPS1, CARDIF, KIAA1271"	Mitochondrial antiviral signaling protein	MAVS	57506	ENSG00000088888			Mavs (MGI:2444773)			
chr20	3888822	3933086	20p13-p12.3	20p13		606157	"PANK2, NBIA1, PKAN, HARP"	Pantothenate kinase 2	PANK2	80025	ENSG00000125779		"HARP syndrome, 607236 (3), Autosomal recessive; Neurodegeneration with brain iron accumulation 1, 234200 (3), Autosomal recessive"	Pank2 (MGI:1921700)			
chr20	3917493	3917570	20p13	20p13		613188	"MIR103-2, MIRN103-2"	Micro RNA 103-2	MIR103A2	406896							
chr20	3927308	4015590	20p13-p12.1	20p13		612489	"RNF24, G1L"	Ring finger protein 24	RNF24	11237	ENSG00000101236			Rnf24 (MGI:1261771)			
chr20	4148778	4187746	20p13	20p13		615854	"SMOX, SMO, PAO1, C20orf16, PAOH"	Spermine oxidase	SMOX	54498	ENSG00000088826			Smox (MGI:2445356)			
chr20	4220630	4249011	20p13	20p13		104219	"ADRA1D, ADRA1A"	"Adrenergic, alpha-1D-, receptor"	ADRA1D	146	ENSG00000171873	incorrectly assigned to 5q		Adra1d (MGI:106673)			
chr20	4686093	4701589	20pter-p12	20p13		176640	"PRNP, PRIP, KURU, CJD"	Prion protein (p27-30)	PRNP	5621	ENSG00000171867	pter-PRNP-SCG1-BMP2A-PAX1-cen	"Cerebral amyloid angiopathy, PRNP-related, 137440 (3), Autosomal dominant; Creutzfeldt-Jakob disease, 123400 (3), Autosomal dominant; Gerstmann-Straussler disease, 137440 (3), Autosomal dominant; Huntington disease-like 1, 603218 (3), Autosomal dominant; Insomnia, fatal familial, 600072 (3), Autosomal dominant; {Kuru, susceptibility to}, 245300 (3); Prion disease with protracted course, 606688 (3), Autosomal dominant"	Prnp (MGI:97769)			
chr20	4721853	4728461	20pter-p12	20p13		604263	"PRND, DPL"	"Prion gene complex, downstream (doppel)"	PRND	23627	ENSG00000171864			"Prn,Prnd (MGI:1346999,MGI:97767)"			
chr20	4852355	5010292	20p13-p12	20p13		603791	"SLC23A2, SVCT2"	"Solute carrier family 23 (nucleobase transporters), member 2 (sodium-dependent vitamin C transporter 2)"	SLC23A2	9962	ENSG00000089057			Slc23a2 (MGI:1859682)			
chr20	5064876	5113090	20p13	20p13-p12		617019	"TMEM230, C20orf30"	Transmembrane protein 230	TMEM230	29058	ENSG00000089063			Tmem230 (MGI:1917862)			
chr20	5100000	9200000	20p12.3			611738	BMND7	Bone mineral density QTL 7		100188853		most significant association with haplotype C	"{Osteoporosis}, 166710 (2), Autosomal dominant"				
chr20	5100000	9200000	20p12.3			612592	CRCS11	"Colorectal cancer, susceptibility to, 11"		100271692		associated with rs961253	"{Colorectal cancer, susceptibility to, 11}, 612592 (2)"				
chr20	5100000	17900000	20p12			608696	"GLC1K, JOAG3"	"Glaucoma 1K, primary open angle, juvenile-onset"	GLC1K	574077		between D20S189 and D20S104	"Glaucoma 1K, primary open angle, juvenile-onset, 608696 (2)"				
chr20	5100000	17900000	20p12			610065	SLEB7	"Systemic lupus erythematosus, susceptibility to, 7"		100188803			"{Systemic lupus erythematosus, susceptibility to, 7}, 610065 (2)"				
chr20	5114952	5126621	20p12	20p12.3		176740	"PCNA, ATLD2"	Proliferating cell nuclear antigen	PCNA	5111	ENSG00000132646	pseudogenes on X and 6; mutation identified in one ATLD2 family	"?Ataxia-telangiectasia-like disorder 2, 615919 (3), Autosomal recessive"	Pcna (MGI:97503)			
chr20	5126760	5197886	20p13	20p12.3		603549	CDS2	CDP-diacylglycerol synthase 2	CDS2	8760	ENSG00000101290			Cds2 (MGI:1332236)			
chr20	5298851	5316731	20p13	20p12.3		607123	"PROKR2, PKR2, GPR73L1, HH3"	Prokineticin receptor 2	PROKR2	128674	ENSG00000101292		"Hypogonadotropic hypogonadism 3 with or without anosmia, 244200 (3), Autosomal dominant"	Prokr2 (MGI:2181363)			
chr20	5544433	5611045	20p12.3	20p12.3		614124	"GPCPD1, GDE5, KIAA1434"	"Glycerophosphocholine phosphodiesterase GDE1, S. cerevisiae, homolog of"	GPCPD1	56261	ENSG00000125772			Gpcpd1 (MGI:104898)			
chr20	5911327	5925360	20pter-p12	20p12.3		118920	"CHGB, SCG1"	Chromogranin B (secretogranin B)	CHGB	1114	ENSG00000089199			Chgb (MGI:88395)			
chr20	5950651	6000940	20p13-p12.3	20p12.3		608187	"MCM8, POF10"	Minichromosome maintenance complement component 8	MCM8	84515	ENSG00000125885	mutation identified in 1 POF10 family	"?Premature ovarian failure 10, 612885 (3), Autosomal recessive"	Mcm8 (MGI:1913884)			
chr20	6005937	6040052	20p13-p12.3	20p12.3		608188	"CRLS1, GCD10, C20orf155"	Cardiolipin synthase 1	CRLS1	54675	ENSG00000088766			Crls1 (MGI:1913836)			
chr20	6074844	6123608	20p13	20p12.3		607900	"KIND1, URP1, C20orf42"	Kindlin 1	FERMT1	55612	ENSG00000101311		"Kindler syndrome, 173650 (3), Autosomal recessive"	Fermt1 (MGI:2443583)			
chr20	6768097	6780279	20p12	20p12.3		112261	"BMP2, BMP2A, BDA2, SSFSC"	Bone morphogenetic protein-2	BMP2	650	ENSG00000125845		"Brachydactyly, type A2, 112600 (3), Autosomal dominant; {HFE hemochromatosis, modifier of}, 235200 (3), Autosomal recessive; Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies, 617877 (3), Autosomal dominant"	Bmp2 (MGI:88177)			
chr20	7882983	7940445	20p12	20p12.3		605023	"HAO1, GOX1"	Hydroxyacid oxidase 1	HAO1	54363	ENSG00000101323			Hao1 (MGI:96011)			
chr20	7977352	8019828	20p12.3	20p12.3		616766	TMX4	Thioredoxin-related transmembrane protein 4	TMX4	56255	ENSG00000125827			Tmx4 (MGI:106558)			
chr20	8132264	8884899	20p12	20p12.3		607120	"PLCB1, KIAA0581, PLCB1A, PLCB1B, EIEE12"	"Phospholipase C, beta-1"	PLCB1	23236	ENSG00000182621		"Epileptic encephalopathy, early infantile, 12, 613722 (3), Autosomal recessive"	Plcb1 (MGI:97613)			
chr20	9068709	9480815	20p12	20p12.3-p12.2		600810	"PLCB4, ARCND2"	"Phospholipase C, beta 4"	PLCB4	5332	ENSG00000101333		"Auriculocondylar syndrome 2, 614669 (3), Autosomal recessive, Autosomal dominant"	Plcb4 (MGI:107464)			
chr20	9514357	9530523	20p12.2	20p12.2		614641	"LAMP5, BADLAMP"	Lysosome-associated membrane protein 5	LAMP5	24141	ENSG00000125869			Lamp5 (MGI:1923411)			
chr20	10218797	10307419	20p11.2	20p12.2		600322	"SNAP25, CMS18"	"Synaptosomal-associated protein, 25kD"	SNAP25	6616	ENSG00000132639	mutation identified in 1 CMS18 patient	"?Myasthenic syndrome, congenital, 18, 616330 (3), Autosomal dominant"	Snap25 (MGI:98331)			
chr20	10404779	10434238	20p12	20p12.2		604896	"MKKS, HMCS, KMS, MKS, BBS6"	McKusick-Kaufman syndrome gene	MKKS	8195	ENSG00000125863		"Bardet-Biedl syndrome 6, 605231 (3), Autosomal recessive; McKusick-Kaufman syndrome, 236700 (3), Autosomal recessive"	Mkks (MGI:1891836)			
chr20	10435135	10628137	20p12.2	20p12.2		615958	"SLX4IP, C20orf94"	SLX4-interacting protein	SLX4IP	128710	ENSG00000149346			Slx4ip (MGI:1921493)			
chr20	10637683	10674045	20p12	20p12.2		601920	"JAG1, AGS1, AHD"	Jagged 1	JAG1	182	ENSG00000101384	mutation identified in 1 DFNCDPE family	"Alagille syndrome 1, 118450 (3), Autosomal dominant; ?Deafness, congenital heart defects, and posterior embryotoxon (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant"	Jag1 (MGI:1095416)			
chr20	11890722	11926594	20p12.2	20p12.2		615566	"BTBD3, KIAA0952"	BTB/POZ domain-containing protein 3	BTBD3	22903	ENSG00000132640						
chr20	13008953	13169102	20p12.3-p12.1	20p12.1		611120	"SPTLC3, SPTLC2L"	"Serine palmitoyltransferase, long-chain base subunit 3"	SPTLC3	55304	ENSG00000172296			Sptlc3 (MGI:2444678)			
chr20	13104759	13638935	20p12.1	20p12.1		608270	"TASP1, C20orf13"	Threonine aspartase 1	TASP1	55617	ENSG00000089123			Tasp1 (MGI:1923062)			
chr20	13221770	13326733	20p12.1	20p12.1		615793	"ISM1, ISM"	"Isthmin 1, angiogenesis inhibitor"	ISM1	140862	ENSG00000101230			Ism1 (MGI:2442963)			
chr20	13785025	13821579	20p12.1	20p12.1		612360	"NDUFAF5, C20orf7"	"NADH dehydrogenase (ubiquinone) complex I, assembly factor T"	NDUFAF5	79133	ENSG00000101247		"Mitochondrial complex 1 deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufaf5 (MGI:1916737)			
chr20	13848585	13995332	20p12.1	20p12.1		614289	SEL1L2	Suppressor of Lin12-like 2	SEL1L2	80343	ENSG00000101251						
chr20	13995499	16053196	20p12	20p12.1		611567	"MACROD2, C2orf133"	Macro domain-containing 2	MACROD2	140733	ENSG00000172264			Macrod2 (MGI:1920149)			
chr20	14322984	14337846	20p11	20p12.1		604808	"FLRT3, HH21"	Fibronectin-like domain-containing leucine-rich transmembrane protein-3	FLRT3	23767	ENSG00000125848		"Hypogonadotropic hypogonadism 21 with anosmia, 615271 (3), Autosomal dominant"	Flrt3 (MGI:1918686)			
chr20	16729963	16741771	20p12.1	20p12.1		603520	SNRPB2	Small nuclear ribonucleoprotein polypeptide B-double prime	SNRPB2	6629	ENSG00000125870			Snrpb2 (MGI:104805)			
chr20	16748352	16752163	20p11	20p12.1		606067	OTOR	Otoraplin	OTOR	56914	ENSG00000125879			Otor (MGI:1888678)			
chr20	17226106	17484577	20p11.2	20p12.1		162151	"PCSK2, NEC2, PC2"	Proprotein convertase subtilisin/kexin type 2	PCSK2	5126	ENSG00000125851			Pcsk2 (MGI:97512)			
chr20	17493904	17569219	20p12.1-p11.23	20p12.1		603307	"BFSP1, CP115, CTRCT33"	Beaded filament structural protein-1 (filensin)	BFSP1	631	ENSG00000125864		"Cataract 33, multiple types, 611391 (3), Autosomal recessive, Autosomal dominant"	Bfsp1 (MGI:101770)			
chr20	17569172	17608241	20p12.1	20p12.1		609114	"DSTN, ADF"	Destrin	DSTN	11034	ENSG00000125868			Dstn (MGI:1929270)			
chr20	17613677	17682282	20p12-p11.2	20p12.1		601418	"RRBP1, ES130"	Ribosome binding protein-1	RRBP1	6238	ENSG00000125844						
chr20	17900000	47800000	20p11.2-q13.12			612406	DYT17	"Dystonia-17, primary torsion"	DYT17	100216344		between D20S472 and D20S911	"Dystonia-17, primary torsion, 612406 (2), Autosomal recessive"				
chr20	17941595	17968990	20p11	20p11.23		605937	SNX5	Sorting nexin 5	SNX5	27131	ENSG00000089006			Snx5 (MGI:1916428)			
chr20	17968593	17991121	20p11.23	20p11.23		615076	"MGME1, C20orf72, MTDPS11"	Mitochondrial genome maintenance exonuclease 1	MGME1	92667	ENSG00000125871		"Mitochondrial DNA depletion syndrome 11, 615084 (3), Autosomal recessive"	Mgme1 (MGI:1921778)			
chr20	18024151	18059187	20p11.23	20p11.23		616441	"OVOL2, ZNF339, PPCD1"	ovo-like 2	OVOL2	58495	ENSG00000125850		"Corneal dystrophy, posterior polymorphous, 1, 122000 (3), Autosomal dominant"	Ovol2 (MGI:1338039)			
chr20	18137854	18143168	20p11.23	20p11.23		614771	PET117	"PET117, S. cerevisiae, homolog of"	PET117	100303755	ENSG00000232838			Pet117 (MGI:5295678)			
chr20	18142223	18188386	20p11.23	20p11.23		617501	"KAT14, CRP2BP, CSRP2BP, ATAC2"	Lysine acetyltransferase 14	KAT14	57325	ENSG00000149474			Kat14 (MGI:1917264)			
chr20	18288227	18316995	20p11.2	20p11.23		604075	ZNF133	Zinc finger protein-133	ZNF133	7692	ENSG00000125846						
chr20	18467388	18484647	20p11.23	20p11.23		617455	"POLR3F, RPC39, RPC6"	"Polymerase III, RNA, subunit F"	POLR3F	10621	ENSG00000132664			Polr3f (MGI:1924086)			
chr20	18486539	18497249	20p11.2	20p11.23		602908	"RBBP9, BOG"	Retinoma-binding protein 9	RBBP9	10741	ENSG00000089050			Rbbp9 (MGI:1347074)			
chr20	18507481	18561414	20p11.2	20p11.23		610512	"SEC23B, CDAN2, HEMPAS, CWS7"	"Sec23, S. cerevisiae, homolog of, B"	SEC23B	10483	ENSG00000101310		"Cowden syndrome 7, 616858 (3), Autosomal dominant; Dyserythropoietic anemia, congenital, type II, 224100 (3), Autosomal recessive"	Sec23b (MGI:1350925)			
chr20	18587892	18763916	20p11	20p11.23		610996	"DTD1, C20orf88"	"D-tyrosyl-tRNA deacylase 1, S. cerevisiae, homolog of"	DTD1	92675	ENSG00000125821			Dtd1 (MGI:1913294)			
chr20	19212645	19722896	20p13	20p11.23		609839	"SLC24A3, NCKX3"	"Solute carrier family 24 (sodium/potassium/calcium exchanger), member 3"	SLC24A3	57419	ENSG00000185052			Slc24a3 (MGI:2137513)			
chr20	19757609	20002458	20p11.22	20p11.23		610222	"RIN2, MACS"	RAS and RAB interactor 2	RIN2	54453	ENSG00000132669		"Macrocephaly, alopecia, cutis laxa, and scoliosis, 613075 (3), Autosomal recessive"	Rin2 (MGI:1921280)			
chr20	20017289	20033628	20p11.2	20p11.23		610833	"NAT5, NAT3"	N-acetyltransferase 5	NAA20	51126	ENSG00000173418			Naa20 (MGI:1915127)			
chr20	20034360	20056045	20p11.2	20p11.23		610952	"CRNKL1, CRN"	Crooked neck pre-mRNA splicing factor-like 1	CRNKL1	51340	ENSG00000101343			Crnkl1 (MGI:1914127)			
chr20	20368120	20370948	20p11.2	20p11.23		600010	"INSM1, IA1"	Insulinoma-associated 1	INSM1	3642	ENSG00000173404			Insm1 (MGI:1859980)			
chr20	21087603	21106357	20p11.23	20p11.23		614992	LINC00237	Long intergenic noncoding RNA 237	LINC00237	105372556							
chr20	21125974	21246621	20p11.23	20p11.23		615757	"KIZ, KIZUNA, C20orf19, RP69"	Kizuna centrosomal protein	KIZ	55857	ENSG00000088970		"Retinitis pigmentosa 69, 615780 (3), Autosomal recessive"	Kiz (MGI:2684960)			
chr20	21300000	22300000	20p11.22			612421	AGA3	"Alopecia, androgenetic, 3"		100217387		associated with rs1160312	"Alopecia, androgenetic, 3, 612421 (2)"				
chr20	21303283	21389824	20p11.2-p11.1	20p11.22		608851	XRN2	Exoribonuclease 2	XRN2	22803	ENSG00000088930			Xrn2 (MGI:894687)			
chr20	21395366	21397408	20p11	20p11.22		607808	"NKX2-4, NKX2D"	NK2 homeobox 4	NKX2-4	644524	ENSG00000125816			Nkx2-4 (MGI:97349)			
chr20	21511009	21514025	20p11	20p11.22		604612	"NKX2-2, NKX2B"	"NK2, homeobox 2"	NKX2-2	4821	ENSG00000125820			Nkx2-2 (MGI:97347)			
chr20	21705658	21718485	20p11.2	20p11.22		167411	"PAX1, OFC2"	Paired box homeotic gene-1	PAX1	5075	ENSG00000125813	mutation identified in 1 family	"?Otofaciocervical syndrome 2, 615560 (3), Autosomal recessive"	Pax1 (MGI:97485)			
chr20	22581003	22585462	20p11	20p11.21		600288	"FOXA2, HNF3B"	"Forkhead box A2 (hepatic nuclear factor-3, beta)"	FOXA2	3170	ENSG00000125798			Foxa2 (MGI:1347476)			
chr20	23035419	23036676	20p11.2	20p11.21		182454	SSTR4	Somatostatin receptor-4	SSTR4	6754	ENSG00000132671			Sstr4 (MGI:105372)			
chr20	23045632	23049663	20p11.2	20p11.21		188040	"THBD, THRM, AHUS6, THPH12"	Thrombomodulin	THBD	7056	ENSG00000178726		"{Hemolytic uremic syndrome, atypical, susceptibility to, 6}, 612926 (3), Autosomal dominant; Thrombophilia due to thrombomodulin defect, 614486 (3)"	Thbd (MGI:98736)			
chr20	23076553	23086829	20p11.21	20p11.21		120577	"C1QR1, CD93, C1QR"	"Complement component 1, q subcomponent, receptor 1"	CD93	22918	ENSG00000125810			Cd93 (MGI:106664)			
chr20	23350735	23354771	20p12-p11.2	20p11.21		605811	"NXT1, MTR2"	NTF2-related export protein 1	NXT1	29107	ENSG00000132661			Nxt1 (MGI:1929619)			
chr20	23361584	23375398	20p11.21	20p11.21		613842	"GZF1, ZNF336, JLSM"	GDNF-inducible zinc finger protein 1	GZF1	64412	ENSG00000125812		"Joint laxity, short stature, and myopia, 617662 (3), Autosomal recessive"	Gzf1 (MGI:1921783)			
chr20	23374518	23421518	20p11.21	20p11.21		611270	"NAPB, SNAPB"	"N-ethylmaleimide-sensitive factor attachment protein, beta"	NAPB	63908	ENSG00000125814			Napb (MGI:104562)			
chr20	23450403	23452844	20p11.21	20p11.21		609731	"CST11, CST8L"	Cystatin 11	CST11	140880	ENSG00000125831			Cst11 (MGI:1925490)			
chr20	23564731	23568748	20p11.2	20p11.21		616536	CST9L	Cystatin 9-like	CST9L	128821	ENSG00000101435			Cst9 (MGI:1340053)			
chr20	23602409	23605972	20p11.2	20p11.21		616543	"CST9, CLM"	Cystatin 9	CST9	128822	ENSG00000173335						
chr20	23627896	23638047	20p11.2	20p11.21		604312	"CST3, ARMD11"	Cystatin C	CST3	1471	ENSG00000101439	proximal to 20p11.2	"Cerebral amyloid angiopathy, 105150 (3), Autosomal dominant; {Macular degeneration, age-related, 11}, 611953 (3)"	Cst3 (MGI:102519)			
chr20	23685639	23689024	20p11.2	20p11.21		123857	CST4	Cystatin S	CST4	1472	ENSG00000101441						
chr20	23747552	23750936	20p11.2	20p11.21		123855	CST1	Cystatin SN	CST1	1469	ENSG00000170373						
chr20	23823766	23826674	20p11.2	20p11.21		123856	CST2	Cystatin SA	CST2	1470	ENSG00000170369						
chr20	23875934	23879742	20p11.21	20p11.21		123858	CST5	Cystatin D	CST5	1473	ENSG00000170367			Cst10 (MGI:1930004)			
chr20	23985052	23989133	20p11.1	20p11.21		612338	"GGTLC1, GGTL6, GGTLA4"	"Gamma-glutamyltransferase, light chain 1"	GGTLC1	92086	ENSG00000149435						
chr20	24469198	24666616	20p11.21	20p11.21		614311	"SYNDIG1, TMEM90B"	Synapse differentiation-induced gene 1	SYNDIG1	79953	ENSG00000101463			Syndig1 (MGI:3702158)			
chr20	24949229	24959927	20p11.2	20p11.21		603253	"CST7, CMAP"	Cystatin 7	CST7	8530	ENSG00000077984			Cst7 (MGI:1298217)			
chr20	24962924	24992929	20p11.2	20p11.21		615884	"APMAP, C20orf3, BSCV"	Adipocyte plasma membrane-associated protein	APMAP	57136	ENSG00000101474			Apmap (MGI:1919131)			
chr20	25006229	25058181	20p11.23-p11.21	20p11.21		614355	"ACSS1, ACECS1"	"Acyl-CoA synthetase short-chain family, member 1"	ACSS1	84532	ENSG00000154930			Acss1 (MGI:1915988)			
chr20	25069939	25082378	20p11.2	20p11.21		605020	"VSX1, RINX, KTCN1, CAASDS"	"Visual system homeo box gene 1, zebrafish, homolog of"	VSX1	30813	ENSG00000100987	mutation identified in 1 CAASDS family	"?Craniofacial anomalies and anterior segment dysgenesis syndrome, 614195 (3); Keratoconus 1, 148300 (3), Autosomal dominant"	Vsx1 (MGI:1890816)			
chr20	25195669	25228074	20q11.2	20p11.21		603160	"ENTPD6, CD39L2"	Ectonucleoside triphosphate diphosphohydrolase 6	ENTPD6	955	ENSG00000197586			Entpd6 (MGI:1202295)			
chr20	25248038	25298011	20p11.2-p11.1	20p11.21		138550	PYGB	"Phosphorylase, glycogen, brain"	PYGB	5834	ENSG00000100994			Pygb (MGI:97828)			
chr20	25294742	25390981	20p11.21	20p11.21		613599	"ABHD12, PHARC"	Abhydrolase domain-containing protein 12	ABHD12	26090	ENSG00000100997		"Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, 612674 (3), Autosomal recessive"	Abhd12 (MGI:1923442)			
chr20	25407469	25448567	20p11.21	20p11.21		610608	"GINS1, PSF1, KIAA0186, IMD55"	GINS complex subunit 1	GINS1	9837	ENSG00000101003		"Immunodeficiency 55, 617827 (3), Autosomal recessive"	Gins1 (MGI:1916520)			
chr20	25612934	25624011	20p11	20p11.21		610763	"NANP, HDHD4"	N-acetylneuraminic acid phosphatase	NANP	140838	ENSG00000170191			Nanp (MGI:1914561)			
chr20	28100000	64444167	20q11-q13			610261	HYT5	"Hypertension, essential, susceptibility to, 5"		100188807			"{Hypertension, essential, susceptibility to, 5}, 145500 (2), Multifactorial"				
chr20	28100000	64444167	20q11-q13			617352	MBCS	Mulchandani-Bhoj-Conlin syndrome				maternal uniparental disomy of imprinted region	"Mulchandani-Bhoj-Conlin syndrome, 617352 (3)"				
chr20	28100000	64444167	20q11-q13			608029	"SCAR6, CLA3"	"Spinocerebellar ataxia, autosomal recessive 6"	CLA3	1167		between D20S471 and D20S119	"Spinocerebellar ataxia, autosomal recessive 6, 608029 (2), Autosomal recessive"				
chr20	30400000	39000000	20q11.2			612263	CMM7	"Melanoma, cutaneous malignant, susceptibility to, 7"		100190932		between rs910873 and rs1885120	"{Melanoma, cutaneous malignant, 7}, 612263 (2)"				
chr20	30400000	43100000	20q11.2-q12			601308	"MLRL, MTS"	Myeloid leukemia-related locus (myeloid tumor suppressor)		8201							
chr20	31368617	31373922	20q11	20q11.21		607650	"DEFB118, C20orf63, ESC42"	"Defensin, beta, 118"	DEFB118	117285	ENSG00000131068						
chr20	31377162	31390648	20q11.1	20q11.21		615997	"DEFB119, DEFB120, DEFB20"	"Defensin, beta, 119"	DEFB119	245932	ENSG00000180483			Defb19 (MGI:2385955)			
chr20	31404844	31418521	20q11.1	20q11.21		616075	"DEFB121, DEFB21"	"Defensin, beta, 121"	DEFB121	245934	ENSG00000204548						
chr20	31421438	31429179	20q11.1	20q11.21		616077	"DEFB122, DEFB22"	"Defensin, beta, 122, pseudogene"	DEFB122	245935							
chr20	31440518	31450256	20q11.1	20q11.21		616076	"DEFB123, DEFB23"	"Defensin, beta, 123"	DEFB123	245936	ENSG00000180424						
chr20	31475272	31484904	20q11.21	20q11.21		610388	"REM1, GES"	RRAD- and GEM-like GTPase 1	REM1	28954	ENSG00000088320			Rem1 (MGI:1097696)			
chr20	31514409	31569566	20q11.21	20q11.21		607106	"HM13, SPP"	Minor histocompatibility 13 (signal peptide peptidase)	HM13	81502	ENSG00000101294			H13 (MGI:95886)			
chr20	31605282	31606514	20q11	20q11.21		600349	ID1	"Inhibitor of DNA binding 1, dominant negative"	ID1	3397	ENSG00000125968			Id1 (MGI:96396)			
chr20	31637855	31645008	20q11.21	20q11.21		607976	COX4I2	"Cytochrome c oxidase, subunit IV, isoform 2"	COX4I2	84701	ENSG00000131055		"Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, 612714 (3), Autosomal recessive"	Cox4i2 (MGI:2135755)			
chr20	31664451	31723998	20q11.21	20q11.21		600039	"BCL2L1, BCLX, BCLXL, BCLXS"	BCL2-like 1	BCL2L1	598	ENSG00000171552			Bcl2l1 (MGI:88139)			
chr20	31739100	31801801	20q11.2	20q11.21		605917	"C20orf1, P100"	"Proliferation-associated nuclear protein, 100kD"	TPX2	22974	ENSG00000088325			Tpx2 (MGI:1919369)			
chr20	31819374	31834696	20q13.3	20q11.21		606566	"MYLK2, MLCK"	Myosin light chain kinase 2	MYLK2	85366	ENSG00000101306		"Cardiomyopathy, hypertrophic, 1, digenic, 192600 (3), Autosomal dominant"	Mylk2 (MGI:2139434)			
chr20	31844299	31845616	20q11.1-q11.2	20q11.21		602939	"FOXS1, FKHL18, FREAC10"	Forkhead box S1	FOXS1	2307	ENSG00000179772			Foxs1 (MGI:95546)			
chr20	31845577	31870743	20q11.21	20q11.21		616776	"DUSP15, VHY"	Dual-specificity phosphatase 15	DUSP15	128853	ENSG00000149599			Dusp15 (MGI:1934928)			
chr20	31944954	31952079	20q11	20q11.21		610789	"PDRG1, PDRG, C20orf126"	P53 and DNA damage-regulated 1	PDRG1	81572	ENSG00000088356			Pdrg1 (MGI:1915809)			
chr20	32052187	32101855	20q11-q12	20q11.21		142370	HCK	Hemopoietic cell kinase	HCK	3055	ENSG00000101336			Hck (MGI:96052)			
chr20	32109505	32167257	20q11.21	20q11.21		617727	"TM9SF4, KIAA0255"	"Transmembrane 9 superfamily, member 4"	TM9SF4	9777	ENSG00000101337			Tm9sf4 (MGI:2139220)			
chr20	32192503	32207742	20q11.21	20q11.21		604866	PLAGL2	Pleomorphic adenoma gene-like 2	PLAGL2	5326	ENSG00000126003			Plagl2 (MGI:1933165)			
chr20	32207888	32238663	20q11.21	20q11.21		607491	"POFUT1, OFUCT1, KIAA0180, DDD2"	Protein O-fucosyltransferase 1	POFUT1	23509	ENSG00000101346		"Dowling-Degos disease 2, 615327 (3), Autosomal dominant"	Pofut1 (MGI:2153207)			
chr20	32277650	32335010	20q11.21	20q11.21		603754	"KIF3B, KIAA0359"	Kinesin family member 3B	KIF3B	9371	ENSG00000101350			Kif3b (MGI:107688)			
chr20	32358061	32439318	20q11.21	20q11.21		612990	"ASXL1, KIAA0978, BOPS, MDS"	Additional sex combs-like 1	ASXL1	171023	ENSG00000171456		"Bohring-Opitz syndrome, 605039 (3), Autosomal dominant; Myelodysplastic syndrome, somatic, 614286 (3)"	Asxl1 (MGI:2684063)			
chr20	32702690	32744007	20q11.21	20q11.21		616703	COMMD7	COMM domain-containing protein 7	COMMD7	149951	ENSG00000149600			Commd7 (MGI:1914197)			
chr20	32762384	32809355	20q11.2	20q11.21		602900	"DNMT3B, ICF1"	DNA methyltransferase 3B	DNMT3B	1789	ENSG00000088305		"Immunodeficiency-centromeric instability-facial anomalies syndrome 1, 242860 (3), Autosomal recessive"	Dnmt3b (MGI:1261819)			
chr20	32819779	32850404	20q11.1-q11.23	20q11.21		603108	"MAPRE1, EB1"	"Microtubule-associated protein, RP/EB family, member 1"	MAPRE1	22919	ENSG00000101367			Mapre1 (MGI:891995)			
chr20	32983772	33004448	20q11.2	20q11.21		613942	"SUN5, TSARG4, SPAG4L, SPGF16"	Sad1 and Unc84 domain-containing protein 5	SUN5	140732	ENSG00000167098		"Spermatogenic failure 16, 617187 (3), Autosomal recessive"	Sun5 (MGI:1923657)			
chr20	33007577	33023708	20q11	20q11.21		614108	"BPIFB2, BPIL1"	"BPI fold-containing protein, family B, member 2"	BPIFB2	80341	ENSG00000078898			Bpifb2 (MGI:1913807)			
chr20	33031647	33044107	20q11	20q11.21		614110	"BPIFB6, BPIL3"	"BPI fold-containing protein, family B, member 6"	BPIFB6	128859	ENSG00000167104			Bpifb6 (MGI:2684965)			
chr20	33055330	33073636	20q11.21	20q11.21		615717	"BPIFBP3, RYA3"	"BPI fold-containing protein, family B, member 3"	BPIFB3	359710	ENSG00000186190			Bpifb3 (MGI:2675077)			
chr20	33081511	33111750	20q11.21	20q11.21		615718	"BPIFB4, RY2G5"	"BPI fold-containing protein, family B, member 4"	BPIFB4	149954	ENSG00000186191			Bpifb4 (MGI:2685852)			
chr20	33193604	33210461	20q11.21	20q11.21		607627	BASE	Breast cancer- and salivary gland-expressed gene	BPIFA4P	317716							
chr20	33235995	33243308	20q11	20q11.21		607412	"BPIFA1, PLUNC, SPLUNC1"	"BPI fold-containing protein, family A, member 1"	BPIFA1	51297	ENSG00000198183			Bpifa1 (MGI:1338036)			
chr20	33358838	33403029	20q11.2	20q11.21		608200	CDK5RAP1	CDK5 regulatory subunit-associated protein 1	CDK5RAP1	51654	ENSG00000101391			Cdk5rap1 (MGI:1914221)			
chr20	33407956	33443891	20q11.2	20q11.21		601017	"SNTA1, SNT1, TACIP1, LQT12"	"Syntrophin, alpha-1"	SNTA1	6640	ENSG00000101400		"Long QT syndrome 12, 612955 (3), Autosomal dominant"	Snta1 (MGI:101772)			
chr20	33490069	33650030	20q11.2	20q11.21-q11.22		603672	"CBFA2T2, MTGR1, EHT"	"Core-binding factor, runt domain, alpha subunit 2, translocated to, 2 (ETO homolog on chromosome 20)"	CBFA2T2	9139	ENSG00000078699			Cbfa2t2 (MGI:1333833)			
chr20	33500000	35800000	20q11.22			612228	STQTL14	Stature quantitative trait locus 14		100270797		associated with rs6060373	"{Stature QTL 14}, 612228 (2)"				
chr20	33657086	33674457	20q11.22	20q11.22		612478	"NECAB3, EFCBP3, NIP1, APBA2BP, XB51, STIP3"	N-terminal EF-hand calcium-binding protein 3	NECAB3	63941	ENSG00000125967			Necab3 (MGI:1861721)			
chr20	33675485	33686403	20q11.2	20q11.22		189971	E2F1	E2F transcription factor-1	E2F1	1869	ENSG00000101412			E2f1 (MGI:101941)			
chr20	33702743	33720329	20q11.22	20q11.22		616397	"PXMP4, PMP24"	Peroxisomal membrane protein 4	PXMP4	11264	ENSG00000101417			Pxmp4 (MGI:1891701)			
chr20	33811303	33854366	20q11.21	20q11.22		610897	"CHMP4B, SNF7, CTPP3, CTRCT31"	"CHMP family, member 4B"	CHMP4B	128866	ENSG00000101421		"Cataract 31, multiple types, 605387 (3), Autosomal dominant"	Chmp4b (MGI:1922858)			
chr20	34186492	34269343	20q11.2	20q11.22		600201	"ASIP, AGTIL, SHEP9"	"Agouti, mouse, signaling protein"	ASIP	434	ENSG00000101440		"[Skin/hair/eye pigmentation 9, brown/nonbrown eyes], 611742 (3); [Skin/hair/eye pigmentation 9, dark/light hair], 611742 (3)"	a (MGI:87853)			
chr20	34235011	34311975	20cen-q13.1	20q11.22		180960	"AHCY, SAHH"	S-adenosylhomocysteine hydrolase	AHCY	191	ENSG00000101444	~13cM from ADA	"Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase, 613752 (3), Autosomal recessive"	Ahcy (MGI:87968)			
chr20	34363234	34511772	20q11.22-q11.23	20q11.22		606409	"ITCH, AIP4, NAPP1, ADMFD"	"Itchy, mouse, homolog of"	ITCH	83737	ENSG00000078747		"Autoimmune disease, multisystem, with facial dysmorphism, 613385 (3), Autosomal recessive"	Itch (MGI:1202301)			
chr20	34516383	34540957	20q12-q13.11	20q11.22		607167	"DYNLRB1, DNCL2A, DNLC2A"	"Dynein, light chain, roadblock type, 1"	DYNLRB1	83658	ENSG00000125971			Dynlrb1 (MGI:1914318)			
chr20	34546822	34560344	20cen-q13	20q11.22		601242	"MAP1ALC3, MAP1BLC3"	"Microtubule-associated proteins 1A and 1B, light chain 3"	MAP1LC3A	84557	ENSG00000101460			Map1lc3a (MGI:1915661)			
chr20	34560541	34677284	20q11.22	20q11.22		608528	"PIGU, CDC91L1"	Phosphatidylinositol glycan anchor biosynthesis class U protein	PIGU	128869	ENSG00000101464			Pigu (MGI:3039607)			
chr20	34704307	34713438	20q11.2	20q11.22		617549	"TP53INP2, PIGU, DOR, C20orf110"	Tumor protein p53-inducible nuclear protein 2	TP53INP2	58476	ENSG00000078804			Trp53inp2 (MGI:1915978)			
chr20	34714773	34825648	20q11	20q11.22		605299	"NCOA6, ASC2, RAP250, NRC, PRIP"	Nuclear receptor coactivator 6	NCOA6	23054	ENSG00000198646						
chr20	34844719	34872857	20q11.2	20q11.22		612342	"GGT7, GGTL3, GGTL5, GGT4"	Gamma-glutamyltransferase 7	GGT7	2686	ENSG00000131067			Ggt7 (MGI:1913385)			
chr20	34874941	34927965	20q11.22	20q11.22		605832	"ACSS2, ACS"	Acetyl-CoA synthetase short-chain family member 2	ACSS2	55902	ENSG00000131069			Acss2 (MGI:1890410)			
chr20	34928432	34956026	20q11.2	20q11.22		601002	"GSS, GSHS"	Glutathione synthetase	GSS	2937	ENSG00000100983		"Glutathione synthetase deficiency, 266130 (3), Autosomal recessive; Hemolytic anemia due to glutathione synthetase deficiency, 231900 (3), Autosomal recessive"	Gss (MGI:95852)			
chr20	34955834	35002436	20q11.22	20q11.22		609928	"MYH7B, MYH14, KIAA1512"	"Myosin, heavy chain 7B, cardiac muscle, beta"	MYH7B	57644	ENSG00000078814			Myh7b (MGI:3710243)			
chr20	34990375	34990496	20q11.22	20q11.22		613614	"MIR499, MIRN499"	Micro RNA 499	MIR499A	574501							
chr20	35002403	35092834	20q11.23	20q11.22		608430	"TRPC4AP, TRUSS"	TRPC4-associated protein	TRPC4AP	26133	ENSG00000100991			Trpc4ap (MGI:1930751)			
chr20	35115356	35147357	20q11.22	20q11.22		610302	EDEM2	Endoplasmic reticulum degradation-enhancing alpha-mannosidase-like protein 2	EDEM2	55741	ENSG00000088298			Edem2 (MGI:1915540)			
chr20	35171936	35215988	20q11.2	20q11.22		600646	"PROCR, EPCR, CCCA, CCD41"	Protein C receptor	PROCR	10544	ENSG00000101000			Procr (MGI:104596)			
chr20	35226735	35277000	20q11.2	20q11.22		604871	MMP25	Matrix metalloproteinase 24	MMP24	10893	ENSG00000125966			Mmp24 (MGI:1341867)			
chr20	35278905	35284815	20q11.2	20q11.22		602912	"EIF6, EIF3A, ITGB4BP"	Eukaryotic translation initiation factor 6	EIF6	3692	ENSG00000242372			Eif6 (MGI:1196288)			
chr20	35302565	35412141	20q11.22	20q11.22		611797	"UQCC, CBP3, BFZB, C20orf44"	Ubiquinol-cytochrome C reductase complex chaperone	UQCC1	55245	ENSG00000101019			Uqcc1 (MGI:1929472)			
chr20	35433346	35454745	20q11.2	20q11.22		601146	"GDF5, CDMP1, SYNS2, OS5, BDA1C, SYM1B"	Growth/differentiation factor-5 (cartilage-derived morphogenetic protein-1)	GDF5	8200	ENSG00000125965	mutation identified in 1 AMDHT family	"?Acromesomelic dysplasia, Hunter-Thompson type, 201250 (3), Autosomal recessive; Brachydactyly, type A1, C, 615072 (3), Autosomal recessive, Autosomal dominant; Brachydactyly, type A2, 112600 (3), Autosomal dominant; Brachydactyly, type C, 113100 (3), Autosomal dominant; Chondrodysplasia, Grebe type, 200700 (3), Autosomal recessive; Du Pan syndrome, 228900 (3), Autosomal recessive; Multiple synostoses syndrome 2, 610017 (3), Autosomal dominant; {Osteoarthritis-5}, 612400 (3); Symphalangism, proximal, 1B, 615298 (3)"	Gdf5 (MGI:95688)			
chr20	35455136	35517530	20q11.2	20q11.22		609689	"CEP2, CEP250, CNAP1"	Centrosomal protein 2	CEP250	11190	ENSG00000126001			Cep250 (MGI:108084)			
chr20	35542028	35557633	20q11.22	20q11.22		616971	"ERGIC3, C2orf47"	Endoplasmic reticulum-golgi intermediate compartment protein 3	ERGIC3	51614	ENSG00000125991			Ergic3 (MGI:1913616)			
chr20	35615855	35621093	20q11.2	20q11.22		603038	SPAG4	Sperm-associated antigen-4	SPAG4	6676	ENSG00000061656			Spag4 (MGI:2444120)			
chr20	35626030	35664955	20q11.22	20q11.22		604205	"CPNE1, CPN1"	Copine I	CPNE1	8904	ENSG00000214078			Cpne1 (MGI:2386621)			
chr20	35648924	35664955	20q11.2	20q11.22		607179	"RBM12, KIAA0765, SCZD19"	RNA-binding motif protein 12	RBM12	10137	ENSG00000244462		"{Schizophrenia 19, susceptibility to}, 617629 (3), Autosomal dominant"	Rbm12 (MGI:1922960)			
chr20	35668687	35699364	20q11.22	20q11.22		603485	"NFS1, NIFS"	Nitrogen fixation gene 1	NFS1	9054	ENSG00000244005			Nfs1 (MGI:1316706)			
chr20	35703608	35742335	20q11.22	20q11.22		604739	"RBM39, CAPER, RNPC2"	RNA binding motif protein 39	RBM39	9584	ENSG00000131051			Rbm39 (MGI:2157953)			
chr20	35772000	35950371	20q11.1-q11.23	20q11.22-q11.23		610335	"PHF20, GLEA2, HCA58"	PHD finger protein 20	PHF20	51230	ENSG00000025293			Phf20 (MGI:2444148)			
chr20	35953616	35955358	20q11.23	20q11.23		610416	"SCAND1, RAZ1, SDP1"	SCAN domain-containing 1	SCAND1	51282	ENSG00000171222			Scand1 (MGI:1343132)			
chr20	36045617	36050959	20q11.23	20q11.23		617037	"NORAD, LINC00657"	Noncoding RNA activated by DNA damage	NORAD	647979							
chr20	36064890	36232798	20q11.2-q12	20q11.23		602879	"EPB41L1, MRD11"	Erythrocyte membrane protein band 4.1-like 1	EPB41L1	2036	ENSG00000088367	mutation identified in 1 patient	"?Mental retardation, autosomal dominant 11, 614257 (3)"	Epb41l1 (MGI:103010)			
chr20	36236135	36256940	20q11.23	20q11.23		617365	"AAR2, C20orf4"	"Aar2 splicing factor, S. cerevisiae, homolog of"	AAR2	25980	ENSG00000131043			Aar2 (MGI:1915545)			
chr20	36306322	36528636	20q11.23	20q11.23		616191	"DLGAP4, SAPAP4, KIAA0964"	Discs LARGE-associated protein 4	DLGAP4	22839	ENSG00000080845	noncoding RNAs transcribed from intron 1 are expressed in all tissues		Dlgap4 (MGI:2138865)			
chr20	36541483	36549822	20q11.23	20q11.23		609905	"MYL9, MLC2"	"Myosin light chain 9, regulatory"	MYL9	10398	ENSG00000101335			Myl9 (MGI:2138915)			
chr20	36573472	36593951	20q11.2-q12	20q11.23		607294	TGIF2	Transforming growth factor-beta-induced factor 2	TGIF2	60436	ENSG00000118707			Tgif2 (MGI:1915299)			
chr20	36612518	36646215	20q11.23	20q11.23		606577	"SLA2, SLAP2"	SRC-like adaptor 2	SLA2	84174	ENSG00000101082			Sla2 (MGI:1925049)			
chr20	36651765	36746137	20q11.21-q11.23	20q11.23		605273	NDRG3	N-myc downstream-regulated gene 3	NDRG3	57446	ENSG00000101079			Ndrg3 (MGI:1352499)			
chr20	36751790	36773826	20q11.23	20q11.23		609175	"DSN1, C20orf172"	"DSN1 homolog, MIS12 kinetochore complex component"	DSN1	79980	ENSG00000149636			Dsn1 (MGI:1914184)			
chr20	36890881	36951842	20q11.2	20q11.23		606754	"SAMHD1, AGS5, DCIP, CHBL2"	SAM domain- and HD domain-containing protein 1	SAMHD1	25939	ENSG00000101347	mutation identified in 1 CHBL2 family	"Aicardi-Goutieres syndrome 5, 612952 (3), Autosomal recessive; ?Chilblain lupus 2, 614415 (3), Autosomal dominant"	Samhd1 (MGI:1927468)			
chr20	36996348	37096214	20q11.2	20q11.23		116957	"RBL1, CP107"	Retinoblastoma-like 1 (p107)	RBL1	5933	ENSG00000080839			Rbl1 (MGI:103300)			
chr20	37179045	37241622	20q12-q13.1	20q11.23		180490	RPN2	Ribophorin II	RPN2	6185	ENSG00000118705			Rpn2 (MGI:98085)			
chr20	37251085	37261816	20q11.2	20q11.23		139190	"GHRH, GHRF"	Growth hormone releasing hormone (somatocrinin)	GHRH	2691	ENSG00000118702		Gigantism due to GHRF hypersecretion (1); ?Isolated growth hormone deficiency due to defect in GHRF (1)	Ghrh (MGI:95709)			
chr20	37344684	37405431	20q12-q13	20q11.23		190090	"SRC, ASV, SRC1, THC6"	"Protooncogene SRC, Rous sarcoma"	SRC	6714	ENSG00000197122	mutation identified in 1 THC6 family	"Colon cancer, advanced, somatic, 114500 (3); ?Thrombocytopenia 6, 616937 (3), Autosomal dominant"	Src (MGI:98397)			
chr20	37517416	37527930	20q11.2-q12	20q11.23		613110	"BLCAP, BC10"	Bladder cancer-associated protein	BLCAP	10904	ENSG00000166619			Blcap (MGI:1858907)			
chr20	37521205	37523689	20q11.2-q12	20q11.23		603106	NNAT	Neuronatin	NNAT	4826	ENSG00000053438			Nnat (MGI:104716)			
chr20	37693954	37872128	20q11.2-q12	20q11.23		611537	"CTNNBL1, NAP"	"Catenin, beta-like, 1"	CTNNBL1	56259	ENSG00000132792			Ctnnbl1 (MGI:1913892)			
chr20	37903096	37945349	20q11.23	20q11.23		616537	"VSTM2L, C20orf102"	V-SET and transmembrane domains-containing protein 2-like	VSTM2L	128434	ENSG00000132821			Vstm2l (MGI:2685537)			
chr20	37983006	38033467	20q11.23	20q11.23		614425	"TTI1, KIAA0406"	TELO2-interacting protein 1	TTI1	9675	ENSG00000101407			Tti1 (MGI:1922675)			
chr20	38033461	38092365	20q11.23	20q11.23		614694	"RPRD1B, CREPT"	Regulation of nuclear pre-mRNA domain-containing protein 1B	RPRD1B	58490	ENSG00000101413			Rprd1b (MGI:1917720)			
chr20	38127386	38166577	20q11.2-q12	20q11.23		190196	TGM2	"Transglutaminase-2 (C polypeptide, protein-glutamine-gamma-glutamyltransferase)"	TGM2	7052	ENSG00000198959			Tgm2 (MGI:98731)			
chr20	38304149	38337504	20q11.23-q12	20q11.23		109195	BPI	Bactericidal/permeability-increasing protein	BPI	671	ENSG00000101425			Bpi (MGI:3045315)			
chr20	38346410	38377010	20q11.23-q12	20q11.23		151990	LBP	Lipopolysaccharide-binding protein	LBP	3929	ENSG00000129988			Lbp (MGI:1098776)			
chr20	38581194	38588462	20q11.23	20q11.23		611396	"ADIG, SMAF1"	Adipogenin	ADIG	149685	ENSG00000182035						
chr20	38724461	38729371	20q11.23	20q11.23		616440	"SLC32A1, VGAT, VIAAT"	"Solute carrier family 32 (GABA vesicular transporter), member 1"	SLC32A1	140679	ENSG00000101438			Slc32a1 (MGI:1194488)			
chr20	38805692	38923023	20q11.22-q12	20q11.23		613275	"PPP1R16B, TIMAP, KIAA0823"	"Protein phosphatase 1, regulatory subunit 16B"	PPP1R16B	26051	ENSG00000101445			Ppp1r16b (MGI:2151841)			
chr20	39000000	51200000	20q12-q13.1			603694	NIDDM3	Noninsulin-dependent diabetes mellitus 3		50982			"{Diabetes mellitus, noninsulin-dependent}, 125853 (2), Autosomal dominant"				
chr20	39000000	47800000	20q12-q13.12			613938	PSMNSW	"Parasomnia, sleepwalking type"		100653383		between 55.6 and 61.4 cM	"Parasomnia, sleepwalking type, 613938 (2), Autosomal dominant, Multifactorial"				
chr20	40004460	40008528	20q11.23	20q12		617038	"LINC01370, HILNC25"	Long intergenic noncoding RNA 1370	LINC01370	100505663							
chr20	40685847	40689239	20q11.2-q13.1	20q12		608968	"MAFB, KRML, MCTO, DURS3"	"v-MAF musculoaponeurotic fibrosarcoma oncogene family, protein B"	MAFB	9935	ENSG00000204103		"Duane retraction syndrome 3, 617041 (3), Autosomal dominant; Multicentric carpotarsal osteolysis syndrome, 166300 (3), Autosomal dominant"	Mafb (MGI:104555)			
chr20	41028817	41124486	20q12-q13.1	20q12		126420	TOP1	Topoisomerase (DNA) I	TOP1	7150	ENSG00000198900	pseudogenes on chr.1 and 22	"DNA topoisomerase I, camptothecin-resistant (3)"	Top1 (MGI:98788)			
chr20	41137518	41175720	20q12-q13.1	20q12		172420	"PLCG1, PLC1"	"Phospholipase C, gamma 1 (formerly subtype 148)"	PLCG1	5335	ENSG00000124181			Plcg1 (MGI:97615)			
chr20	41178448	41317639	20q12	20q12		609598	"ZHX3, KIAA0395"	Zinc finger and homeodomain protein-3	ZHX3	23051	ENSG00000174306			Zhx3 (MGI:2444772)			
chr20	41340778	41360584	20q	20q12		605520	LPIN3	Lipin 3	LPIN3	64900	ENSG00000132793			Lpin3 (MGI:1891342)			
chr20	41402100	41618493	20q11.23-q12	20q12		616114	"CHD6, CHD5, RIGB"	Chromodomain helicase DNA-binding protein 6	CHD6	84181	ENSG00000124177			Chd6 (MGI:1918639)			
chr20	42029958	43189916	20q12-q13.1	20q12-q13		608712	"PTPRT, KIAA0283"	"Protein-tyrosine phosphatase, receptor-type, T"	PTPRT	11122	ENSG00000196090			Ptprt (MGI:1321152)			
chr20	43100000	64444167	20q13			608878	GEVQ2	"Gene expression, variation in, quantitative trait locus on chromosome 20"		474333			"{Gene expression, variation in, QTL}, 608878 (2)"				
chr20	43100000	43500000	20q13.11			603388	GRD2	"Graves disease, susceptibility to, 2"		50976			"{Graves disease, susceptibility to, 2}, 603388 (2)"				
chr20	43100000	64444167	20q13			608656	HPC3	"Prostate cancer, hereditary, 3"		408259			"{Prostate cancer, susceptibility to, 3}, 176807 (2), Autosomal dominant"				
chr20	43100000	64444167	20q13			612566	IBD24	Inflammatory bowel disease 24		100270798		associated with rs2315008 and rs4809330	"{Inflammatory bowel disease 24}, 612566 (2)"				
chr20	43100000	64444167	20q13			612950	PSORS12	Psoriasis susceptibility 12				associated with rs495337	"{Psoriasis susceptibility 12}, 612950 (2)"				
chr20	43100000	64444167	20q13			610066	SLEB8	"Systemic lupus erythematosus, susceptibility to, 8"		100188804			"{Systemic lupus erythematosus, susceptibility to, 8}, 610066 (2)"				
chr20	43457863	43463604	20q13.11	20q13.11		601944	"SRSF6, SFRS6, SRp55"	"Splicing factor, serine/arginine-rich, 6"	SRSF6	6431	ENSG00000124193			Srsf6 (MGI:1915246)			
chr20	43507679	43541894	20q12	20q13.12		608802	"L3MBTL, L3MBTL1, KIAA0681"	L3MBT-like	L3MBTL1	26013	ENSG00000185513			L3mbtl1 (MGI:2676663)			
chr20	43558994	43585632	20q13.2	20q13.12		607589	SGK2	Serum/glucocorticoid-regulated kinase 2	SGK2	10110	ENSG00000101049			Sgk2 (MGI:1351318)			
chr20	43590612	43647295	20q13.12	20q13.12		617094	IFT52	"Intraflagellar transport 52, Chlamydomonas, homolog of"	IFT52	51098	ENSG00000101052		"Short-rib thoracic dysplasia 16 with or without polydactyly, 617102 (3), Autosomal recessive"	Ift52 (MGI:2387217)			
chr20	43667018	43716495	20q13.1	20q13.12		601415	"MYBL2, BMYB"	v-myb avian myeloblastosis viral oncogene homolog-like 2	MYBL2	4605	ENSG00000101057			Mybl2 (MGI:101785)			
chr20	43914851	44069615	20q13.12	20q13.12		611163	"TOX2, GCX1, C20orf100"	TOX high mobility group box family member 2	TOX2	84969	ENSG00000124191			Tox2 (MGI:3611233)			
chr20	44111696	44187945	20q12	20q13.12		605267	"JPH2, JP2, CMH17"	Junctophilin 2	JPH2	57158	ENSG00000149596		"Cardiomyopathy, hypertrophic, 17, 613873 (3), Autosomal dominant"	Jph2 (MGI:1891496)			
chr20	44302837	44311251	20q13.12	20q13.12		612029	"FIT2, C20orf142"	Fat-inducing transcript 2	FITM2	128486	ENSG00000197296			Fitm2 (MGI:2444508)			
chr20	44355800	44432844	20q12-q13.1	20q13.12		600281	"HNF4A, TCF14, MODY1, FRTS4"	"Hepatocyte nuclear factor 4, alpha (transcription factor-14)"	HNF4A	3172	ENSG00000101076		"{Diabetes mellitus, noninsulin-dependent}, 125853 (3), Autosomal dominant; Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, 616026 (3), Autosomal dominant; MODY, type I, 125850 (3), Autosomal dominant"	Hnf4a (MGI:109128)			
chr20	44496220	44522115	20q13.1-q13.3	20q13.12		607165	"SERINC3, TDE1"	Serine incorporator 3	SERINC3	10955	ENSG00000132824			Serinc3 (MGI:1349457)			
chr20	44531780	44619036	20q	20q13.12		604932	PKIG	"Protein kinase, cAMP-dependent catalytic, inhibitor gamma"	PKIG	11142	ENSG00000168734			Pkig (MGI:1343086)			
chr20	44619518	44651757	20q13.11	20q13.12		608958	ADA	Adenosine deaminase	ADA	100	ENSG00000196839		"Adenosine deaminase deficiency, partial, 102700 (3), Autosomal recessive, Somatic mosaicism; Severe combined immunodeficiency due to ADA deficiency, 102700 (3), Autosomal recessive, Somatic mosaicism"	Ada (MGI:87916)			
chr20	44714203	44728040	20q12-q13	20q13.12		603399	WISP2	Wnt-1 inducible signaling pathway protein 2	WISP2	8839	ENSG00000064205			Wisp2 (MGI:1328326)			
chr20	44745604	44752312	20q12-q13	20q13.12		607368	"KCNK15, TASK5"	"Potassium channel, subfamily K, member 15"	KCNK15	60598	ENSG00000124249			Kcnk15 (MGI:2675209)			
chr20	44751803	44810337	20q13.3	20q13.12		611601	RIMS4	Protein regulating synaptic membrane exocytosis 4	RIMS4	140730	ENSG00000101098			Rims4 (MGI:2674366)			
chr20	44885598	44908531	20q13.1	20q13.12		601289	YWHAB	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide"	YWHAB	7529	ENSG00000166913			Ywhab (MGI:1891917)			
chr20	44942129	44960472	20q13.12	20q13.12		616049	"TOMM34, TOM34"	"Translocase of outer mitochondrial membrane 34, yeast, homolog of"	TOMM34	10953	ENSG00000025772			Tomm34 (MGI:1914395)			
chr20	44966469	45079976	20q13.2	20q13.12		604965	"STK4, MST1, KRS2, TIIAC"	Serine/threonine protein kinase 4	STK4	6789	ENSG00000101109		"T-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations, 614868 (3)"	Stk4 (MGI:1929004)			
chr20	45091213	45101111	20q13.12	20q13.12		602905	"KCNS1, KV9.1"	"Potassium channel, voltage-gated, delayed-rectifier, subfamily S, member 1"	KCNS1	3787	ENSG00000124134			Kcns1 (MGI:1197019)			
chr20	45109451	45116320	20q12-q13.2	20q13.12		605161	"WFDC5, PRG5, WAP1"	WAP 4-disulfide core domain 5	WFDC5	149708	ENSG00000175121			Wfdc5 (MGI:2384800)			
chr20	45123425	45124464	20q12-q13.1	20q13.12		609872	"WFDC12, WAP2, SWAM2"	Wap 4-disulfide core domain 12	WFDC12	128488	ENSG00000168703						
chr20	45174898	45176543	20q12-q13	20q13.12		182257	PI3	"Protease inhibitor 3, skin derived (SKALP)"	PI3	5266	ENSG00000124102						
chr20	45206963	45209772	20q12-q13.1	20q13.12		182140	"SEMG1, SEMG"	Semenogelin	SEMG1	6406	ENSG00000124233						
chr20	45221368	45224457	20q12-q13.1	20q13.12		182141	SEMG2	Semenogelin II	SEMG2	6407	ENSG00000124157						
chr20	45252238	45254563	20q13.12	20q13.12		107285	"SLPI, HUSI"	Secretory leukocyte protease inhibitor	SLPI	6590	ENSG00000124107			Slpi (MGI:109297)			
chr20	45293445	45308565	20q13.1-q13.2	20q13.12		603897	MATN4	Matrilin 4	MATN4	8785	ENSG00000124159			Matn4 (MGI:1328314)			
chr20	45306835	45319676	20q13.12	20q13.12		616104	"RBPJL, RBPL, SUHL"	RBPJ-like protein	RBPJL	11317	ENSG00000124232			Rbpjl (MGI:1196616)			
chr20	45325287	45348423	20q12-q13	20q13.12		600017	SDC4	"Syndecan 4 (amphiglycan, ryudocan)"	SDC4	6385	ENSG00000124145			Sdc4 (MGI:1349164)			
chr20	45361936	45376801	20q13.12	20q13.12		612979	SYS1	"Sys1 golgi-localized integral membrane protein, S. cerevisiae, homolog of"	SYS1	90196	ENSG00000204070			Sys1 (MGI:1913710)			
chr20	45373879	45378549	20q13.12	20q13.12		617316	TP53TG5	TP53 target gene 5	TP53TG5	27296	ENSG00000124251			Trp53tg5 (MGI:1920853)			
chr20	45405992	45410609	20q12	20q13.12		611453	"DBNDD2, HSMNP1"	Dysbindin domain-containing 2	DBNDD2	55861	ENSG00000244274			Dbndd2 (MGI:106562)			
chr20	45416066	45426244	20q13.12	20q13.12		610272	"PIGT, NDAP, PNH2, MCAHS3"	"Phosphatidylinositol glycan, class T"	PIGT	51604	ENSG00000124155	mutation identified in 1 PNH2 family	"Multiple congenital anomalies-hypotonia-seizures syndrome 3, 615398 (3), Autosomal recessive; ?Paroxysmal nocturnal hemoglobinuria 2, 615399 (3), Autosomal dominant, Somatic mutation"	Pigt (MGI:1926178)			
chr20	45469753	45481531	20q13.12	20q13.12		617548	"WFDC2, HE4, WAP5"	WAP 4-disulfide core domain 2	WFDC2	10406	ENSG00000101443			Wfdc2 (MGI:1914951)			
chr20	45512460	45515623	20q12-q13.1	20q13.12		613941	SPINT3	"Serin protease inhibitor, Kunitz-type, 3"	SPINT3	10816	ENSG00000101446						
chr20	45540625	45547425	20q13.2	20q13.12		609031	"SPINLW1, EPPIN, WAP7"	Serine protease inhibitor-like protein with Kunitz and WAP domains 1	EPPIN	57119	ENSG00000101448			Wfdc6a (MGI:2684968)			
chr20	45791936	45811426	20q13.12	20q13.12		611388	"DNTTIP1, TDIF1, C20orf167"	"Deoxynucleotidyltransferase, terminal, interacting protein 1"	DNTTIP1	116092	ENSG00000101457			Dnttip1 (MGI:1923483)			
chr20	45812575	45816956	20q13.12	20q13.12		605574	"UBE2C, UBCH10"	Ubiquitin-conjugating enzyme E2C	UBE2C	11065	ENSG00000175063			Ube2c (MGI:1915862)			
chr20	45823213	45833328	20q12-q13.11	20q13.12		191039	TNNC2	"Troponin C2, fast"	TNNC2	7125	ENSG00000101470			Tnnc2 (MGI:98780)			
chr20	45841720	45857408	20q13.1	20q13.12		608123	"ACOT8, PTE1"	Acyl-CoA thioesterase 8	ACOT8	10005	ENSG00000101473			Acot8 (MGI:2158201)			
chr20	45890143	45898819	20q13.1	20q13.12		613111	"CTSA, PPGB, GSL, NGBE, GLB2"	Cathepsin A (protective protein for beta-galactosidase)	CTSA	5476	ENSG00000064601		"Galactosialidosis, 256540 (3), Autosomal recessive"	Ctsa (MGI:97748)			
chr20	45898619	45912363	20q12-q13.1	20q13.12		172425	"PLTP, HDLCQ9"	Phospholipid transfer protein	PLTP	5360	ENSG00000100979		[High density lipoprotein cholesterol level QTL 9] (3)	Pltp (MGI:103151)			
chr20	45948652	45972909	20q11.2-q13.1	20q13.12		610827	"ZNF335, NIF1, NIF2, MCPH10"	Zinc finger protein 335	ZNF335	63925	ENSG00000198026	mutation identified in 1 MCPH10 family	"?Microcephaly 10, primary, autosomal recessive, 615095 (3), Autosomal recessive"	Zfp335 (MGI:2682313)			
chr20	46008907	46016560	20q11.2-q13.1	20q13.12		120361	"MMP9, CLG4B, MANDP2"	"Matrix metalloproteinase 9 (gelatinase B, 92kD type IV collagenase)"	MMP9	4318	ENSG00000100985		"Metaphyseal anadysplasia 2, 613073 (3)"	Mmp9 (MGI:97011)			
chr20	46021689	46060149	20q12-q13.1	20q13.12		606726	"SLC12A5, KCC2, KIAA1176, EIEE34, EIG14"	"Solute carrier family 12, (potassium-chloride transporter) member 5"	SLC12A5	57468	ENSG00000124140		"{Epilepsy, idiopathic generalized, susceptibility to, 14}, 616685 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 34, 616645 (3), Autosomal recessive"	Slc12a5 (MGI:1862037)			
chr20	46060984	46089940	20q13.1	20q13.12		616825	"NCOA5, CIA"	Nuclear receptor coactivator 5	NCOA5	57727	ENSG00000124160			Ncoa5 (MGI:2385165)			
chr20	46118241	46129744	20q12-q13.2	20q13.12		109535	"CD40, TNFRSF5"	CD40 antigen	CD40	958	ENSG00000101017		"Immunodeficiency with hyper-IgM, type 3, 606843 (3), Autosomal recessive"	Cd40 (MGI:88336)			
chr20	46173732	46308497	20q13.1	20q13.12		609920	CDH22	Cadherin 22	CDH22	64405	ENSG00000149654			Cdh22 (MGI:1341843)			
chr20	46366044	46407050	20q13	20q13.12		606421	"ELMO2, CED12, VMPI"	Engulfment and cell motility gene 2	ELMO2	63916	ENSG00000062598		"Vascular malformation, primary intraosseous, 606893 (3), Autosomal recessive"	Elmo2 (MGI:2153045)			
chr20	46557822	46684484	20q12-q13.1	20q13.12		606411	"SLC13A3, NADC3"	"Solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3"	SLC13A3	64849	ENSG00000158296			Slc13a3 (MGI:2149635)			
chr20	46684364	46689636	20q13.12	20q13.12		608679	"TP53RK, PRPK, GAMOS4"	TP53-regulating kinase	TP53RK	112858	ENSG00000172315		"Galloway-Mowat syndrome 4, 617730 (3), Autosomal recessive"	"Trp53rkb,Trp53rka (MGI:1918294,MGI:1914050)"			
chr20	46708357	46736346	20q13.1	20q13.12		606145	"SLC2A10, GLUT10, ATS"	"Solute carrier family 2 (facilitated glucose transporter), member 10"	SLC2A10	81031	ENSG00000197496		"Arterial tortuosity syndrome, 208050 (3), Autosomal recessive"	Slc2a10 (MGI:2156687)			
chr20	46894623	47188843	20q13.1	20q13.12		601654	EYA2	"Eyes absent, Drosophila, homolog of, 2"	EYA2	2139	ENSG00000064655			Eya2 (MGI:109341)			
chr20	47209213	47357779	20q13.12	20q13.12		615713	"ZMYND8, PRKCBP1"	Zinc finger MYND domain-containing protein 8	ZMYND8	23613	ENSG00000101040			Zmynd8 (MGI:1918025)			
chr20	47501856	47656876	20q12	20q13.12		601937	"NCOA3, AIB1, TNRC14"	Nuclear receptor coactivator 3 (amplified in breast cancer-1)	NCOA3	8202	ENSG00000124151			Ncoa3 (MGI:1276535)			
chr20	47654568	47786615	20q13.12	20q13.12		610013	"SULF2, KIAA1247"	Sulfatase 2	SULF2	55959	ENSG00000196562			Sulf2 (MGI:1919293)			
chr20	48624251	48827882	20q13.13	20q13.13		606905	"PREX1, KIAA1415"	"Phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 1"	PREX1	57580	ENSG00000124126			Prex1 (MGI:3040696)			
chr20	48921720	49036692	20q13.13	20q13.13		605371	"ARFGEF2, BIG2, PVNH2"	"ADP-ribosylation factor guanine nucleotide-exchange factor 2, brefeldin A-inhibited"	ARFGEF2	10564	ENSG00000124198		"Periventricular heterotopia with microcephaly, 608097 (3), Autosomal recessive"	Arfgef2 (MGI:2139354)			
chr20	49046245	49096959	20q13	20q13.13		601342	"CSE1L, CAS"	"Chromosome segregation-1, yeast, homolog of, like"	CSE1L	1434	ENSG00000124207			Cse1l (MGI:1339951)			
chr20	49113338	49219294	20q13.1	20q13.13		601716	"STAU1, STAU"	"Staufen, Drosophila, homolog of, 1"	STAU1	6780	ENSG00000124214			Stau1 (MGI:1338864)			
chr20	49219294	49244076	20q13.13	20q13.13		616621	"DDX27, RHLP"	DEAD box polypeptide 27	DDX27	55661	ENSG00000124228			Ddx27 (MGI:2385884)			
chr20	49363876	49484032	20q13.2	20q13.13		600397	"KCNB1, EIEE26"	"Potassium voltage-gated channel, Shab-related subfamily, member 1"	KCNB1	3745	ENSG00000158445		"Epileptic encephalopathy, early infantile, 26, 616056 (3), Autosomal dominant"	Kcnb1 (MGI:96666)			
chr20	49503873	49568169	20q13.11-q13.13	20q13.13		601699	"PTGIS, CYP8A1, PGIS, CYP8"	Prostaglandin I2 synthase	PTGIS	5740	ENSG00000124212		"Hypertension, essential, 145500 (3), Multifactorial"	Ptgis (MGI:1097156)			
chr20	49632944	49713883	20q13.1-q13.2	20q13.13		604016	B4GALT5	"Beta-1,4-galactosyltransferase 5"	B4GALT5	9334	ENSG00000158470	previously mapped to chr.11		B4galt5 (MGI:1927169)			
chr20	49812712	49892241	20q13.13	20q13.13		612730	"SLC9A8, NHE8, KIAA0939"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 8"	SLC9A8	23315	ENSG00000197818			Slc9a8 (MGI:1924281)			
chr20	49903390	49915542	20q13.1-q13.2	20q13.13		607662	"SPATA2, KIAA0757"	Spermatogenesis-associated protein 2	SPATA2	9825	ENSG00000158480			Spata2 (MGI:2146885)			
chr20	49936376	49953884	20q13	20q13.13		612451	"RNF114, ZNF313"	Ring finger protein 114	RNF114	55905	ENSG00000124226			Rnf114 (MGI:1933159)			
chr20	49982975	49988885	20q13.1	20q13.13		604238	SNAI1	"Snail 1, Drosophila, homolog of"	SNAI1	6615	ENSG00000124216	pseudogene on 2q34		Snai1 (MGI:98330)			
chr20	50081123	50115958	20q13.2	20q13.13		602995	"UBE2V1, UEV1"	Ubiquitin-conjugating enzyme E2 variant 1	UBE2V1	7335	ENSG00000244687			Ube2v1 (MGI:1913839)			
chr20	50123736	50153797	20q13.2	20q13.13		610994	"TMEM189, KUA"	Transmembrane protein 189	TMEM189	387521	ENSG00000240849			Tmem189 (MGI:2142624)			
chr20	50190582	50192689	20q13.1	20q13.13		189965	"CEBPB, TCF5"	"CCAAT/enhancer-binding protein (C/EBP), beta (transcription factor-5)"	CEBPB	1051	ENSG00000172216			Cebpb (MGI:88373)			
chr20	50510320	50584761	20q13.1-q13.2	20q13.13		176885	"PTPN1, PTP1B"	"Protein tyrosine phosphatase, nonreceptor-type, 1"	PTPN1	5770	ENSG00000196396	20pter-q12 by REa	"{Insulin resistance, susceptibility to}, 125853 (3), Autosomal dominant"	Ptpn1 (MGI:97805)			
chr20	50731543	50753740	20q13.13	20q13.13		608975	PARD6B	"Partitioning-defective protein 6, C. elegans, homolog of, beta"	PARD6B	84612	ENSG00000124171			Pard6b (MGI:2135605)			
chr20	50794893	50877735	20q13.13	20q13.13		607471	BCAS4	Breast carcinoma amplified sequence 4	BCAS4	55653	ENSG00000124243						
chr20	50888917	50931212	20q13.13	20q13.13		611386	"ADNP, ADNP1, KIAA0784, HVDAS, MRD28"	Activity-dependent neuroprotector homeobox	ADNP	23394	ENSG00000101126		"Helsmoortel-van der Aa syndrome, 615873 (3), Autosomal dominant"	Adnp (MGI:1338758)			
chr20	50934854	50958563	20q13.13	20q13.13		603503	"DPM1, MPDS, CDGIE"	"Dolichyl-phosphate mannosyltransferase 1, catalytic subunit"	DPM1	8813	ENSG00000000419		"Congenital disorder of glycosylation, type Ie, 608799 (3), Autosomal recessive"	Dpm1 (MGI:1330239)			
chr20	51003655	51023175	20q13	20q13.13		603788	"KCNG1, KH2"	"Potassium voltage-gated channel, subfamily G, member 1"	KCNG1	3755	ENSG00000026559			Kcng1 (MGI:3616086)			
chr20	51200000	64444167	20q13.2-q13.3			610248	DFNB65	"Deafness, autosomal recessive 65"	DFNB65	692219		max lod at D20S840	"Deafness, autosomal recessive 65, 610248 (2), Autosomal recessive"				
chr20	51200000	64444167	20q13.2-q13.3			130180	"EEGV1, EEGL"	Electroencephalographic variant pattern 1	EEGV1	1940							
chr20	51386956	51562856	20q13.2-q13.3	20q13.2		600490	"NFATC2, NFATP"	"Nuclear factor of activated T cells, cytoplasmic, calcineurin-dependent 2"	NFATC2	4773	ENSG00000101096			Nfatc2 (MGI:102463)			
chr20	51782716	51802522	20q13.13-q13.2	20q13.2		607343	"SALL4, HSAL4"	sal-like 4	SALL4	57167	ENSG00000101115		"Duane-radial ray syndrome, 607323 (3), Autosomal dominant; IVIC syndrome, 147750 (3), Autosomal dominant"	Sall4 (MGI:2139360)			
chr20	52972308	53495329	20q13.2	20q13.2		614118	TSHZ2	Teashirt zinc finger homeobox 2	TSHZ2	128553	ENSG00000182463			Tshz2 (MGI:2153084)			
chr20	53567064	53608968	20q13.2	20q13.2		602967	ZNF217	Zinc finger protein-217	ZNF217	7764	ENSG00000171940			Zfp217 (MGI:2685408)			
chr20	53943537	54070764	20q13.2	20q13.2		602968	"BCAS1, NABC1"	Breast carcinoma amplified sequence	BCAS1	8537	ENSG00000064787			Bcas1 (MGI:1924210)			
chr20	54145730	54174031	20q13.2-q13.3	20q13.2		126065	"CYP24A1, CYP24, HCINF1"	"Cytochrome P450, family 24, subfamily A, polypeptide 1 (vitamin D 24-hydroxylase)"	CYP24A1	1591	ENSG00000019186		"Hypercalcemia, infantile, 1, 143880 (3), Autosomal recessive"	Cyp24a1 (MGI:88593)			
chr20	54207962	54219952	20q13.2	20q13.2		604898	"PFDN4, C1"	Prefoldin 4	PFDN4	5203	ENSG00000101132			Pfdn4 (MGI:1923512)			
chr20	54475471	54651170	20q13.2	20q13.2		608334	DOK5	Docking protein 5	DOK5	55816	ENSG00000101134			Dok5 (MGI:1924079)			
chr20	55997356	56005471	20q13.2	20q13.2		615029	CBLN4	Precerebellin 4	CBLN4	140689	ENSG00000054803			Cbln4 (MGI:2154433)			
chr20	56248731	56249814	20q13.2	20q13.2		155540	"MC3R, BMIQ9"	Melanocortin-3 receptor	MC3R	4159	ENSG00000124089		"{Mycobacterium tuberculosis, protection against}, 607948 (3); {Obesity, severe, susceptibility to, BMIQ9}, 602025 (3)"	Mc3r (MGI:96929)			
chr20	56369388	56392336	20q13.2-q13.3	20q13.2		603072	"AURKA, STK15, AURORA2, BTAK, ARK1, STK6, AIK"	Aurora kinase A	AURKA	6790	ENSG00000087586		"{Colon cancer, susceptibility to}, 114500 (3), Autosomal dominant"	Aurka (MGI:894678)			
chr20	56392370	56404525	20q13.2	20q13.2-q13.3		600369	CSTF1	"Cleavage stimulation factor, 3' pre-RNA, subunit 1, 50kD"	CSTF1	1477	ENSG00000101138			Cstf1 (MGI:1914587)			
chr20	56400000	64444167	20q13.31-q13.33			612929	MTBS3	"Mycobacterium tuberculosis, susceptibility to, 3"		100302686		associated with rs3827103	"{Mycobacterium tuberculosis, susceptibility to, 3}, 612929 (2)"				
chr20	56629301	56639282	20q13.2	20q13.31		601602	TFAP2C	Transcription factor AP-2 gamma (activating enhancer-binding protein 2 gamma)	TFAP2C	7022	ENSG00000087510			Tfap2c (MGI:106032)			
chr20	57168752	57266650	20q13.1-q13.3	20q13.31		112267	BMP7	Bone morphogenetic protein-7 (osteogenic protein-1)	BMP7	655	ENSG00000101144			Bmp7 (MGI:103302)			
chr20	57329756	57343992	20q13.2-q13.3	20q13.31		605114	SPO11	"Spo11, S. cerevisiae, homolog of"	SPO11	23626	ENSG00000054796			Spo11 (MGI:1349669)			
chr20	57391397	57409332	20q13.31	20q13.31		612428	"RBM38, RNPC1"	RNA-binding motif protein 38	RBM38	55544	ENSG00000132819			Rbm38 (MGI:1889294)			
chr20	57495964	57525651	20q13.2	20q13.31		607022	"CTCFL, BORIS"	CCCTC-binding factor-like protein	CTCFL	140690	ENSG00000124092			Ctcfl (MGI:3652571)			
chr20	57561080	57566460	20q13.31	20q13.31		614168	"PCK1, PCKDC"	Phosphoenolpyruvate carboxykinase-1 (soluble)	PCK1	5105	ENSG00000124253	mutation identified in 1 PCKDC family	"?Phosphoenolpyruvate carboxykinase deficiency, cytosolic, 261680 (3), Autosomal recessive"	Pck1 (MGI:97501)			
chr20	57603845	57620575	20q13.31	20q13.31		606750	"ZBP1, C20orf183, DLM1"	Z-DNA binding protein 1 (tumor stroma and activated macrophage protein DLM1)	ZBP1	81030	ENSG00000124256			Zbp1 (MGI:1927449)			
chr20	57648391	57711535	20q13	20q13.31		606564	"PMEPA1, TMEPAI"	"Prostate transmembrane protein, androgen-induced"	PMEPA1	56937	ENSG00000124225			Pmepa1 (MGI:1929600)			
chr20	58309714	58367506	20q13.3	20q13.32		612966	RAB22A	Ras-associated protein RAB22A	RAB22A	57403	ENSG00000124209			Rab22a (MGI:105072)			
chr20	58389118	58451100	20q13.3	20q13.32		605704	"VAPB, VAPC, ALS8"	Vesicle-associated membrane protein-associated protein B	VAPB	9217	ENSG00000124164		"Amyotrophic lateral sclerosis 8, 608627 (3), Autosomal dominant; Spinal muscular atrophy, late-onset, Finkel type, 182980 (3), Autosomal dominant"	Vapb (MGI:1928744)			
chr20	58651252	58679525	20q13.32	20q13.32		603666	"STX16, SYN16"	Syntaxin 16	STX16	8675	ENSG00000124222		"Pseudohypoparathyroidism, type IB, 603233 (3), Autosomal dominant"	Stx16 (MGI:1923396)			
chr20	58817614	58817693	20q13.3	20q13.32		610945	"MIR296, MIRN296"	Micro RNA 296	MIR296	407022							
chr20	58818225	58818312	20q13.32	20q13.32		614914	MIR298	Micro RNA 298	MIR298	100126296							
chr20	58818917	58850902	20q13.2	20q13.32		610540	"GNASAS1, GNASAS, SANG, NESPAS"	GNAS antisense RNA 1	GNAS-AS1	149775			"Pseudohypoparathyroidism, type IB, 603233 (3), Autosomal dominant"				
chr20	58839680	58911195	20q13.2	20q13.32		139320	"GNAS, GNAS1, GPSA, POH, PHP1B, PHP1A, AHO, PHP1C, PITA3"	"GNAS complex locus (guanine nucleotide binding protein (G protein), alpha stimulating activity polypeptide 1)"	GNAS	2778	ENSG00000087460		"ACTH-independent macronodular adrenal hyperplasia, 219080 (3), Isolated cases; McCune-Albright syndrome, somatic, mosaic, 174800 (3); Osseous heteroplasia, progressive, 166350 (3), Autosomal dominant; Pituitary adenoma 3, multiple types, somatic, 617686 (3); Pseudohypoparathyroidism Ia, 103580 (3), Autosomal dominant; Pseudohypoparathyroidism Ib, 603233 (3), Autosomal dominant; Pseudohypoparathyroidism Ic, 612462 (3), Autosomal dominant; Pseudopseudohypoparathyroidism, 612463 (3), Autosomal dominant"	Gnas (MGI:95777)			
chr20	58981207	58995132	20q13	20q13.32		605297	"TH1L, TH1"	"TH1, Drosophila, homolog of"	NELFCD	51497	ENSG00000101158			Nelfcd (MGI:1926424)			
chr20	58995186	59007253	20q13	20q13.32		603169	CTSZ	Cathepsin Z	CTSZ	1522	ENSG00000101160			Ctsz (MGI:1891190)			
chr20	59016025	59026653	20q13.3	20q13.32		612901	TUBB1	"Tubulin, beta-1"	TUBB1	81027	ENSG00000101162		"Macrothrombocytopenia, autosomal dominant, TUBB1-related, 613112 (3), Autosomal dominant"	Tubb1 (MGI:107814)			
chr20	59028677	59032366	20q13.3	20q13.32		606153	"ATP5E, MC5DN3"	"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit"	ATP5F1E	514	ENSG00000124172	pseudogene on 4q25; mutation identified in 1 MC5DN3 patient	"?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, 614053 (3)"				
chr20	59300414	59325991	20q13.2-q13.3	20q13.32		131242	"EDN3, WS4B, HSCR4"	Endothelin-3	EDN3	1908	ENSG00000124205		"Central hypoventilation syndrome, congenital, 209880 (3), Autosomal dominant; {Hirschsprung disease, susceptibility to, 4}, 613712 (3), Autosomal dominant; Waardenburg syndrome, type 4B, 613265 (3), Autosomal recessive, Autosomal dominant"	Edn3 (MGI:95285)			
chr20	59577496	59849828	20q13.32	20q13.32-q13.33		608725	"PHACTR3, SCAPININ"	Phosphatase and actin regulator 3	PHACTR3	116154	ENSG00000087495			Phactr3 (MGI:1921439)			
chr20	59700000	64444167	20q13.33			613031	GLM6	Glioma susceptibility 6		100415895		associated with rs6010620	"{Glioma susceptibility 6}, 613031 (2)"				
chr20	59863276	59933699	20q13.33	20q13.33		604105	"SYCP2, SCP2"	Synaptonemal complex protein 2	SYCP2	10388	ENSG00000196074			Sycp2 (MGI:1933281)			
chr20	59936831	59940296	20q13.3	20q13.33		603326	"PPP1R3D, PPP1R6"	"Protein phosphatase 1, regulatory subunit 3D"	PPP1R3D	5509	ENSG00000132825			Ppp1r3d (MGI:1917664)			
chr20	59957763	60037970	20q13.33	20q13.33		617685	CDH26	Cadherin 26	CDH26	60437	ENSG00000124215			Cdh26 (MGI:2685856)			
chr20	61252425	61940616	20q13.3	20q13.33		603006	CDH4	Cadherin 4	CDH4	1002	ENSG00000179242			Cdh4 (MGI:99218)			
chr20	61974797	62065809	20q13.33	20q13.33		601796	"TAF4, TAF2C1, TAFII130, TAF2C"	"TAF4 RNA polymerase II, TATA box-binding protein-associated factor, 135kD"	TAF4	6874	ENSG00000130699			Taf4 (MGI:2152346)			
chr20	62136726	62143457	20q13.33	20q13.33		606607	PSMA7	"Proteasome subunit, alpha-type, 7"	PSMA7	5688	ENSG00000101182			Psma7 (MGI:1347070)			
chr20	62143719	62182509	20q13.3	20q13.33		606472	"SS18L1, KIAA0693, CREST"	SS18-like gene 1	SS18L1	26039	ENSG00000184402			Ss18l1 (MGI:2444061)			
chr20	62182745	62203567	20q13.33	20q13.33		610919	"GTPBP5, OBGH1"	GTP-binding protein 5	MTG2	26164	ENSG00000101181			Mtg2 (MGI:106565)			
chr20	62213844	62220266	20q13.33	20q13.33		604525	"HRH3, GPCR97"	Histamine receptor H3	HRH3	11255	ENSG00000101180			Hrh3 (MGI:2139279)			
chr20	62238484	62296212	20q	20q13.33		606731	"OSBPL2, ORP2, KIAA0772, DNFA67"	Oxysterol-binding protein-like protein 2	OSBPL2	9885	ENSG00000130703		"Deafness, autosomal dominant 67, 616340 (3), Autosomal dominant"	Osbpl2 (MGI:2442832)			
chr20	62302060	62308861	20q13.33	20q13.33		610650	"ADRM1, ARM1, RPN13"	Adhesion-regulating molecule 1	ADRM1	11047	ENSG00000130706			Adrm1 (MGI:1929289)			
chr20	62309059	62367317	20q13.2-q13.3	20q13.33		601033	LAMA5	"Laminin, alpha-5"	LAMA5	3911	ENSG00000130702			Lama5 (MGI:105382)			
chr20	62386274	62388519	20q13.3	20q13.33		180477	RPS21	Ribosomal protein S21	RPS21	6227	ENSG00000171858			Rps21 (MGI:1913731)			
chr20	62463496	62475969	20q13.2-q13.3	20q13.33		611496	"GATA5, CHTD5"	GATA-binding protein 5	GATA5	140628	ENSG00000130700		"Congenital heart defects, multiple types, 5, 617912 (3), Autosomal recessive, Autosomal dominant"	Gata5 (MGI:109497)			
chr20	62554305	62554375	20q13.33	20q13.33		609326	MIR1-1	Micro RNA 1-1	MIR1-1	406904							
chr20	62564911	62565012	20q13.33	20q13.33		610255	MIR133A2	Micro RNA 133A2	MIR133A2	406923							
chr20	62642057	62690721	20q13.33	20q13.33		612436	"SLCO4A1, OATPE, OATP4A1"	"Solute carrier organic anion transporter family, member 4A1"	SLCO4A1	28231	ENSG00000101187			Slco4a1 (MGI:1351866)			
chr20	62708769	62762770	20q13	20q13.33		162651	NTSR1	Neurotensin receptor	NTSR1	4923	ENSG00000101188			Ntsr1 (MGI:97386)			
chr20	62796404	62801737	20q13.33	20q13.33		611157	"MRGBP, C20orf20"	MRG/MORF4L-binding protein	MRGBP	55257	ENSG00000101189			Mrgbp (MGI:1920497)			
chr20	62817061	62841158	20q13.3	20q13.33		120270	"COL9A3, EDM3, IDD"	"Collagen IX, alpha-3 polypeptide"	COL9A3	1299	ENSG00000092758		"Epiphyseal dysplasia, multiple, 3, with or without myopathy, 600969 (3), Autosomal dominant; {Intervertebral disc disease, susceptibility to}, 603932 (3)"	Col9a3 (MGI:894686)			
chr20	62877737	62937951	20q13.33	20q13.33		604140	"DATF1, DIO1"	Death-associated transcription factor 1	DIDO1	11083	ENSG00000101191			Dido1 (MGI:1344352)			
chr20	62938088	62948474	20q13.33	20q13.33		611625	"GID8, C20orf11, TWA1"	"GID complex, subunit 8"	GID8	54994	ENSG00000101193			Gid8 (MGI:1923675)			
chr20	62952646	62968596	20q13.3	20q13.33		612107	"SLC17A9, C20orf59, POROK8"	"Solute carrier family 17, member 9"	SLC17A9	63910	ENSG00000101194		"Porokeratosis 8, disseminated superficial actinic type, 616063 (3), Autosomal dominant"	Slc17a9 (MGI:1919107)			
chr20	63005978	63007034	20q13	20q13.33		609331	"BHLHE23, BHLHB4"	"Basic helix-loop-helix family, member E23"	BHLHE23	128408	ENSG00000125533			Bhlhe23 (MGI:2153710)			
chr20	63095492	63102318	20q13.33	20q13.33		610557	"HAR1B, HAR1R"	Highly accelerated region gene 1B	HAR1B	768097							
chr20	63101291	63104385	20q13.33	20q13.33		610556	"HAR1A, HAR1F"	Highly accelerated region gene 1A	HAR1A	768096							
chr20	63195428	63216185	20q13.33	20q13.33		616529	YTHDF1	YTH N6-methyladenosine RNA-binding protein 1	YTHDF1	54915	ENSG00000149658			Ythdf1 (MGI:1917431)			
chr20	63235882	63240506	20q13.3	20q13.33		605737	"BIRC7, MLIAP, KIAP, LIVIN"	Baculoviral IAP repeat-containing protein 7	BIRC7	79444	ENSG00000101197			Birc7 (MGI:2676458)			
chr20	63240779	63256405	20q13.33	20q13.33		612873	NKAIN4	Na+/K+ transporting ATPase-interacting 4	NKAIN4	128414	ENSG00000101198			Nkain4 (MGI:1915372)			
chr20	63272784	63289792	20q13.33	20q13.33		608377	ARFGAP1	ADP-ribosylation factor GTPase-activating protein 1	ARFGAP1	55738	ENSG00000101199			Arfgap1 (MGI:2183559)			
chr20	63343309	63375470	20q13.2-q13.3	20q13.33		118504	"CHRNA4, ENFL1"	"Cholinergic receptor, nicotinic, alpha polypeptide-4"	CHRNA4	1137	ENSG00000101204		"Epilepsy, nocturnal frontal lobe, 1, 600513 (3), Autosomal dominant; {Nicotine addiction, susceptibility to}, 188890 (3)"	Chrna4 (MGI:87888)			
chr20	63400207	63472676	20q13.3	20q13.33		602235	"KCNQ2, EBN1, EIEE7, BFNS1"	"Potassium voltage-gated channel, KQT-like subfamily, member 2"	KCNQ2	3785	ENSG00000075043		"Epileptic encephalopathy, early infantile, 7, 613720 (3), Autosomal dominant; Myokymia, 121200 (3), Autosomal dominant; Seizures, benign neonatal, 1, 121200 (3), Autosomal dominant"	Kcnq2 (MGI:1309503)			
chr20	63488011	63499314	20q13	20q13.33		602959	"EEF1A2, EIEE33, MRD38"	"Eukaryotic translation elongation factor-1, alpha-2"	EEF1A2	1917	ENSG00000101210		"Epileptic encephalopathy, early infantile, 33, 616409 (3), Autosomal dominant; Mental retardation, autosomal dominant 38, 616393 (3), Autosomal dominant"	Eef1a2 (MGI:1096317)			
chr20	63528412	63537369	20q13.3	20q13.33		602004	"PTK6, BRK"	Protein-tyrosine kinase 6	PTK6	5753	ENSG00000101213			Ptk6 (MGI:99683)			
chr20	63539923	63547503	20q13.33	20q13.33		617797	"SRMS, C20orf148"	Src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites	SRMS	6725	ENSG00000125508			Srms (MGI:101865)			
chr20	63558085	63574238	20q13.3	20q13.33		611265	"PRIC285, PDIP1, KIAA1769"	"Peroxisomal proliferator-activated receptor alpha-interacting cofactor complex, 285kD subunit"	HELZ2	85441	ENSG00000130589			Helz2 (MGI:2385169)			
chr20	63587593	63627100	20q13.33	20q13.33		607451	"GMEB2, KIAA1269"	Glucocorticoid modulatory element-binding protein 2	GMEB2	26205	ENSG00000101216			Gmeb2 (MGI:2652836)			
chr20	63639704	63653609	20q13.3	20q13.33		608362	"STMN3, SCLIP"	Stathmin-like 3	STMN3	50861	ENSG00000197457			Stmn3 (MGI:1277137)			
chr20	63657809	63696252	20q13.3	20q13.33		608833	"RTEL1, C20orf41, NHL, KIAA1088, DKCB5, DKCA4, PFBMFT3"	Regulator of telomere elongation helicase 1	RTEL1	51750	ENSG00000258366		"Dyskeratosis congenita, autosomal dominant 4, 615190 (3), Autosomal recessive, Autosomal dominant; Dyskeratosis congenita, autosomal recessive 5, 615190 (3), Autosomal recessive, Autosomal dominant; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3, 616373 (3), Autosomal dominant"	Rtel1 (MGI:2139369)			
chr20	63696650	63698697	20q13	20q13.33		603361	"TNFRSF6B, DCR3"	"Tumor necrosis factor receptor superfamily, member 6b (decoy receptor 3)"	TNFRSF6B	8771	ENSG00000243509						
chr20	63698641	63708012	20q13.33	20q13.33		604699	"ARFRP1, ARP"	ADP-ribosylation factor-related protein 1	ARFRP1	10139	ENSG00000101246			Arfrp1 (MGI:1923938)			
chr20	63735700	63739106	20q13.3	20q13.33		609809	"LIME1, LIME"	LCK-interacting transmembrane adaptor 1	LIME1	54923	ENSG00000203896			Lime1 (MGI:1919949)			
chr20	63743667	63832331	20q13.33	20q13.33		614639	"ZBTB46, BZEL"	Zinc finger- and BTB domain-containing protein 46	ZBTB46	140685	ENSG00000130584			Zbtb46 (MGI:1919397)			
chr20	63865227	63891544	20q13.2-q13.3	20q13.33		603747	TPD52L2	Tumor protein D52-like 2	TPD52L2	7165	ENSG00000101150			Tpd52l2 (MGI:1913564)			
chr20	63895101	63936030	20q13.33	20q13.33		611203	"DNAJC5, DNAJC5A, CSP, CLN4B"	"DNAJ/HSP40 homolog, subfamily C, member 5"	DNAJC5	80331	ENSG00000101152		"Ceroid lipofuscinosis, neuronal, 4, Parry type, 162350 (3), Autosomal dominant"	Dnajc5 (MGI:892995)			
chr20	63939828	63956446	20q13.33	20q13.33		610866	"UCKL1, UCK1L, URKL1"	Uridine/cytidine kinase-like 1	UCKL1	54963	ENSG00000198276			Uckl1 (MGI:1915806)			
chr20	63956702	63969869	20q13.33	20q13.33		617886	"ZNF512B, KIAA1196"	Zinc finger protein 512B	ZNF512B	57473	ENSG00000196700			Zfp512b (MGI:2685478)			
chr20	63981077	64033099	20q13.33	20q13.33		613979	"PRPF6, PRP6, ANT1, TOM, C20orf14"	"Precursor mRNA-processing factor 6, S. cerevisiae, homolog of"	PRPF6	24148	ENSG00000101161		"Retinitis pigmentosa 60, 613983 (3), Autosomal dominant"	Prpf6 (MGI:1922946)			
chr20	64047725	64049625	20q13.33	20q13.33		601618	"SOX18, HLTS, HLTRS"	"SOX18, mouse, homolog of"	SOX18	54345	ENSG00000203883		"Hypotrichosis-lymphedema-telangiectasia syndrome, 607823 (3), Autosomal recessive; Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome, 137940 (3), Autosomal dominant"	Sox18 (MGI:103559)			
chr20	64073180	64080003	20q13.3	20q13.33		605071	"RGS19, GAIP"	Regulator of G protein signaling 19	RGS19	10287	ENSG00000171700			Rgs19 (MGI:1915153)			
chr20	64080081	64100642	20q13.33	20q13.33		602548	"OPRL1, NOP"	Opioid receptor-like 1	OPRL1	4987	ENSG00000125510			Oprl1 (MGI:97440)			
chr20	64105829	64106830	20q13.3	20q13.33		600731	GPR8	G protein-coupled receptor-8	NPBWR2	2832	ENSG00000125522	related sequence on 14					
chr20	64164473	64242252	20q13.3	20q13.33		600379	"MYT1, PLPB1"	Myelin transcription factor 1	MYT1	4661	ENSG00000196132			Myt1 (MGI:1100535)			
chr20	0	64444167	Chr.20			151310	"HTL, LEUT, HLT"	"Leucine transport, high"	HTL	3343							
chr21	0	15000000	21p13-q11			610838	AUTS12	"Autism, susceptibility to, 12"		100188314		max lod at D21S1437	"{Autism susceptibility 12}, 610838 (2)"				
chr21	3100000	7000000	21p12			180453	RNR4	Ribosomal RNA-4	RNR4	6055							
chr21	7000000	10900000	21p11.2			605167	"BAGE1, BAGE"	"BAGE family, member 1"	BAGE	574		previously assigned to chr.13					
chr21	7000000	10900000	21p11.2			617777	BAGE3	"BAGE family, member 3"	BAGE3	85318							
chr21	10413531	10491614	21p11.2	21p11.2		617776	BAGE2	"BAGE family, member 2"	BAGE2	85319							
chr21	10521513	10606269	21p	21p11.2		604336	TPTE	Transmembrane phosphatase with tensin homology	TPTE	7179	ENSG00000274391						
chr21	13000000	15000000	21q11.2			609039	NRCLP3	Narcolepsy 3		494446		max lod at D21S1245	"Narcolepsy 3, 609039 (2), Autosomal dominant"				
chr21	13000000	15000000	21q11.2			159595	"TAM, MST"	"Myeloproliferative syndrome, transient (transient abnormal myelopoiesis)"		8205			"Leukemia, transient, of Down syndrome, 159595 (2)"				
chr21	13610080	13641584	21q11.2	21q11.2		607549	"POTED, ANKRD21, POTE"	"POTE ankyrin domain family, member D"	POTED	317754	ENSG00000166351						
chr21	14108812	14210952	21q11.2	21q11.2		609252	"LIPI, LPDL, PRED5"	Lipase I	LIPI	149998	ENSG00000188992		"{Hypertriglyceridemia, susceptibility to}, 145750 (3), Autosomal dominant"	Lipi (MGI:2443868)			
chr21	14273798	14301385	21q11.2	21q11.2		608835	ABCC13	"ATP-binding cassette, subfamily C, member 13"	ABCC13	150000							
chr21	14371114	14383187	21q11.1	21q11.2		601100	STCH	"Stress 70 protein chaperone, microsome-associated, p60"	HSPA13	6782	ENSG00000155304			Hspa13 (MGI:1309463)			
chr21	14485227	14583401	21q11.2	21q11.2		607978	"SAMSN1, HACS1"	"SAM domain, SH3 domain, and nuclear localization signals 1"	SAMSN1	64092	ENSG00000155307			Samsn1 (MGI:1914992)			
chr21	14961234	15065902	21q11	21q11.2-q21.1		602490	"NRIP1, RIP140"	Nuclear receptor interacting protein 1 (receptor interacting protein 140)	NRIP1	8204	ENSG00000180530			Nrip1 (MGI:1315213)			
chr21	15000000	30200000	21q21			602097	USH1E	"Usher syndrome-1E, autosomal recessive, severe"	USH1E	7396			"Usher syndrome, type 1E, 602097 (2), Autosomal recessive"				
chr21	16070487	16631726	21q21.1	21q21.1		615964	"MIR99AHG, MONC, LINC00478"	"MIR99A-LET7C cluster host gene, noncoding"	MIR99AHG	388815							
chr21	16539088	16539168	21q21.1	21q21.1		614509	MIR99A	Micro RNA 99A	MIR99A	407055							
chr21	16539827	16539910	21q21.1	21q21.1		612144	"MIRLET7C, MIRNLET7C, LET7C"	Micro RNA Let7c	MIRLET7C	406885							
chr21	16590236	16590324	21q21.1	21q21.1		610105	"MIR125B2, MIRN125B2"	Micro RNA 125B-2	MIR125B2	406912							
chr21	17512905	17636212	21q11.2	21q21.1		602621	"CXADR, CAR"	Coxsackie virus and adenovirus receptor	CXADR	1525	ENSG00000154639	pseudogenes on chr.15 and chr.18		Cxadr (MGI:1201679)			
chr21	17593649	17612949	21q11.2-q21.1	21q21.1		605674	"BTG3, ANA, TOB5"	B-cell translocation gene 3	BTG3	10950	ENSG00000154640			Btg3 (MGI:109532)			
chr21	17819328	18267370	21q21	21q21.1		607247	CHODL	Chondrolectin	CHODL	140578	ENSG00000154645			Chodl (MGI:2179069)			
chr21	18269106	18403805	21q21	21q21.1		606635	"PRSS7, ENTK"	"Protease, serine, 7 (enterokinase)"	TMPRSS15	5651	ENSG00000154646		"Enterokinase deficiency, 226200 (3), Autosomal recessive"	Tmprss15 (MGI:1197523)			
chr21	20998295	21543328	21q21	21q21.1		602040	NCAM2	"Cell adhesion molecule, neural, 2"	NCAM2	4685	ENSG00000154654			Ncam2 (MGI:97282)			
chr21	25573979	25574043	21q21.3	21q21.3		609337	"MIR155, BIC, MIRN155"	Micro RNA 155	MIR155	406947							
chr21	25585655	25607857	21q11.2-q21	21q21.3		611845	"MRPL39, MRPL5"	Mitochondrial ribosomal protein L39	MRPL39	54148	ENSG00000154719			Mrpl39 (MGI:1351620)			
chr21	25607549	25717561	21q21.2	21q21.3		606870	"JAM2, VEJAM"	Junctional adhesion molecule 2	JAM2	58494	ENSG00000154721			Jam2 (MGI:1933820)			
chr21	25724479	25735653	21q21.3	21q21.3		603152	"ATP5J, ATP5"	"ATP synthase, H+ transporting, mitochondrial F0 complex, subunit F6"	ATP5PF	522	ENSG00000154723			Atp5j (MGI:107777)			
chr21	25734946	25772459	21q21-q22.1	21q21.3		600609	"GABPA, E4TF1A"	"GA-binding protein transcription factor, alpha subunit, 60kD"	GABPA	2551	ENSG00000154727			Gabpa (MGI:95610)			
chr21	25880549	26171127	21q21	21q21.3		104760	"APP, AAA, CVAP, AD1"	Amyloid beta (A4) precursor protein	APP	351	ENSG00000142192	proximal to SOD; very distal q21 or boundary with q22	"Alzheimer disease 1, familial, 104300 (3), Autosomal dominant; Cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants, 605714 (3), Autosomal dominant"	App (MGI:88059)			
chr21	26393634	26569251	21q21.3	21q21.3		616021	"CYYR1AS1, CYYR1-AS1"	CYRR1 antisense RNA 1	CYYR1-AS1	100996571							
chr21	26466208	26573403	21q21.3	21q21.3		616020	CYYR1	Cysteine/tyrosine-rich protein 1	CYYR1	116159	ENSG00000166265			Cyyr1 (MGI:2152187)			
chr21	26836286	26845408	21q21.2	21q21.3		605174	"ADAMTS1, METH1"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 1"	ADAMTS1	9510	ENSG00000154734			Adamts1 (MGI:109249)			
chr21	26917911	26967757	21q21-q22	21q21.3		605007	"ADAMTS5, ADAMTS11"	"A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 5 (aggrecanase 2)"	ADAMTS5	11096	ENSG00000154736			Adamts5 (MGI:1346321)			
chr21	28439660	28885372	21q21.3	21q21.3		614553	N6AMT1	"N6 adenine-specific DNA methyltransferase 1, putative"	N6AMT1	29104	ENSG00000156239			N6amt1 (MGI:1915018)			
chr21	28928143	28992987	21q22.11	21q21.3		613083	"LTN1, RNF160, KIAA0714"	Listerin E3 ubiquitin protein ligase 1	LTN1	26046	ENSG00000198862			Ltn1 (MGI:1926163)			
chr21	29005758	29019370	21q22.1	21q21.3		617843	"RWDD2B, C21orf6"	RWD domain-containing protein 2B	RWDD2B	10069	ENSG00000156253			Rwdd2b (MGI:1858215)			
chr21	29024616	29054487	21q21.3	21q21.3		604735	"USP16, UBPM"	Ubiquitin-specific protease 16	USP16	10600	ENSG00000156256			Usp16 (MGI:1921362)			
chr21	29056321	29073796	21q21.3	21q21.3		617786	"CCT8, KIAA0002"	"Chaperonin containing T-complex polypeptide 1, subunit 8"	CCT8	10694	ENSG00000156261			Cct8 (MGI:107183)			
chr21	29077470	29175888	21q21	21q21.3		611110	"TAK1L, C21orf7"	TAK1-like	MAP3K7CL	56911	ENSG00000156265						
chr21	29298794	29361895	21q22.1	21q21.3		602751	BACH1	BTB and CNC homology 1	BACH1	571	ENSG00000156273			Bach1 (MGI:894680)			
chr21	29536932	29940051	21q22	21q21.3		138245	"GRIK1, GLUR5"	"Glutamate receptor, ionotropic, kainate 1"	GRIK1	2897	ENSG00000171189			Grik1 (MGI:95814)			
chr21	30165922	30166652	21q21.3	21q21.3		617005	CLDN17	Claudin 17	CLDN17	26285	ENSG00000156282			Cldn17 (MGI:2652030)			
chr21	30200000	46709983	21q22			611515	7-Feb	"Febrile seizures, familial, 7"	7-Feb	100049160		max lod at D21S1910	"Febrile seizures, familial, 7, 611515 (2)"				
chr21	30200000	46709983	21q22			609428	TUKLS	Tukel syndrome		574049		max lod at D21S1259	"Tukel syndrome, 609428 (2), Autosomal recessive"				
chr21	30214005	30216150	21q22.11	21q22.11		611231	CLDN8	Claudin 8	CLDN8	9073	ENSG00000156284			Cldn8 (MGI:1859286)			
chr21	30396073	30396821	21q22.11	21q22.11		608718	KRTAP13-1	Keratin-associated protein 13-1	KRTAP13-1	140258	ENSG00000198390			Krtap13-1 (MGI:2146359)			
chr21	30880643	30881554	21q22.11	21q22.11		600064	"KRTAP11-1, HACL1"	Keratin-associated protein 11-1	KRTAP11-1	337880	ENSG00000182591			Krtap11-1 (MGI:99447)			
chr21	31118417	31559976	21q22.1	21q22.11		600687	TIAM1	T-cell lymphoma invasion and metastasis 1	TIAM1	7074	ENSG00000156299			Tiam1 (MGI:103306)			
chr21	31659621	31668930	21q22.1	21q22.11		147450	"SOD1, ALS1"	"Superoxide dismutase-1, soluble"	SOD1	6647	ENSG00000142168	mid q22.1	"Amyotrophic lateral sclerosis 1, 105400 (3), Autosomal recessive, Autosomal dominant"	Sod1 (MGI:98351)			
chr21	31668986	31732117	21q22.11	21q22.11		616023	"SCAF4, KIAA1172"	SR-related C-terminal domain-associated factor 4	SCAF4	57466	ENSG00000156304			Scaf4 (MGI:2146350)			
chr21	31873314	32004063	21q22	21q22.11		606532	HUNK	Hormonally upregulated NEU-associated kinase	HUNK	30811	ENSG00000142149			Hunk (MGI:1347352)			
chr21	32291812	32314783	21q22.1	21q22.11		609196	"MRAP, FALP, C21orf61, GCCD2, FGD2"	Melanocortin 2 receptor accessory protein	MRAP	56246	ENSG00000170262		"Glucocorticoid deficiency 2, 607398 (3), Autosomal recessive"	Mrap (MGI:1924287)			
chr21	32311018	32393002	21q22.1	21q22.11		608865	"URB1, NPA1, C21orf108, KIAA0539"	URB1 ribosome biogenesis 1 homolog (S. cerevisiae)	URB1	9875	ENSG00000142207			Urb1 (MGI:2146468)			
chr21	32574840	32585544	21q22.1	21q22.11		608365	TCP10L	T-complex protein 10-like	TCP10L	140290	ENSG00000242220						
chr21	32599353	32612870	21q22.11	21q22.11		615494	"C21orf59, CILD26"	Chromosome 21 open reading frame 59	CFAP298	56683	ENSG00000159079		"Ciliary dyskinesia, primary, 26, 615500 (3), Autosomal recessive"	1110004E09Rik (MGI:1915251)			
chr21	32628758	32731246	21q22.2	21q22.11		604297	"SYNJ1, PARK20, EIEE53"	Synaptojanin 1	SYNJ1	8867	ENSG00000159082		"Epileptic encephalopathy, early infantile, 53, 617389 (3), Autosomal recessive; Parkinson disease 20, early-onset, 615530 (3), Autosomal recessive"	Synj1 (MGI:1354961)			
chr21	32733898	32771857	21q22.11	21q22.11		617621	"PAXBP1, GCFC1, C21orf66"	PAX3- and PAX7-binding protein 1	PAXBP1	94104	ENSG00000159086			Paxbp1 (MGI:1914617)			
chr21	33025907	33029195	21q22.11	21q22.11		606386	"OLIG2, PRKCBP2"	Oligodendrocyte lineage transcription factor 2	OLIG2	10215	ENSG00000205927			Olig2 (MGI:1355331)			
chr21	33070143	33072421	21q22.11	21q22.11		606385	OLIG1	Oligodendrocyte lineage transcription factor 1	OLIG1	116448	ENSG00000184221			Olig1 (MGI:1355334)			
chr21	33229894	33264512	21q22.1	21q22.11		602376	"IFNAR2, IMD45"	"Interferon, alpha, beta, and omega, receptor 2"	IFNAR2	3455	ENSG00000159110	mutation identified in 1 IMD45 family	"{Hepatitis B virus, susceptibility to}, 610424 (3); ?Immunodeficiency 45, 616669 (3), Autosomal recessive"	Ifnar2 (MGI:1098243)			
chr21	33266359	33297233	21q22.1	21q22.11		123889	"CRFB4, IBD25"	"Cytokine receptor, family II, member 4"	IL10RB	3588	ENSG00000243646	35kb distal to IFNAR; D21S58	"{Hepatitis B virus, susceptibility to}, 610424 (3); Inflammatory bowel disease 25, early onset, autosomal recessive, 612567 (3), Autosomal recessive"	Il10rb (MGI:109380)			
chr21	33324442	33360360	21q22.1	21q22.11		107450	IFNAR1	"Interferon, alpha, beta and omega, receptor 1"	IFNAR1	3454	ENSG00000142166			Ifnar1 (MGI:107658)			
chr21	33402895	33437520	21q22.1-q22.2	21q22.11		147569	"IFNGR2, IFNGT1, IFGR2, IMD28"	Interferon gamma receptor-2 (interferon gamma transducer 1)	IFNGR2	3460	ENSG00000159128		"Immunodeficiency 28, mycobacteriosis, 614889 (3), Autosomal recessive"	Ifngr2 (MGI:107654)			
chr21	33432485	33480008	21q22.11	21q22.11		617894	"TMEM50B, C21orf4"	Transmembrane protein 50B	TMEM50B	757	ENSG00000142188			Tmem50b (MGI:1925225)			
chr21	33503930	33542891	21q22.1	21q22.11		138440	"GART, PRGS, PGFT"	Phosphoribosylglycinamide formyltransferase (phosphoribosylglycinamide synthetase; phosphoribosylaminoimidazole synthetase)	GART	2618	ENSG00000159131	"multifunctional protein: Ade(-)C, Ade(-)G, GART"		Gart (MGI:95654)			
chr21	33543037	33577513	21q22.1-q22.2	21q22.11		182465	"SON, TOKIMS"	SON DNA-binding protein	SON	6651	ENSG00000159140		"ZTTK syndrome, 617140 (3), Autosomal dominant"	Son (MGI:98353)			
chr21	33577550	33588707	21q22.1	21q22.11		611428	"DONSON, C21orf60, MISSLA, MIMIS"	Downstream neighbor of SON	DONSON	29980	ENSG00000159147		"Microcephaly, short stature, and limb abnormalities, 617604 (3), Autosomal recessive; Microcephaly-micromelia syndrome, 251230 (3), Autosomal recessive"	Donson (MGI:1890621)			
chr21	33589340	33641853	21q22.1	21q22.11		603920	CRYZL1	"Crystallin, zeta-like 1"	CRYZL1	9946	ENSG00000205758			Cryzl1 (MGI:1913859)			
chr21	33642399	33899860	21q22.1-q22.2	21q22.11		602442	"ITSN1, SH3D1A, SH3P17"	Intersectin 1 (SH3 domain protein-1A)	ITSN1	6453	ENSG00000205726			Itsn1 (MGI:1338069)			
chr21	33903452	33915853	21q22.1-q22.2	21q22.11		600828	ATP5O	"ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit (oligomycin sensitivity conferring protein)"	ATP5PO	539	ENSG00000241837			Atp5o (MGI:106341)			
chr21	34073522	34143033	21q21.3-q22.1	21q22.11		611973	MRPS6	Mitochondrial ribosomal protein S6	MRPS6	64968	ENSG00000243927			Mrps6 (MGI:2153111)			
chr21	34073522	34106261	21q22	21q22.11		600444	SLC5A3	"Solute carrier family 5 (inositol transporter), member 3"	SLC5A3	6526	ENSG00000198743	?role in Down syndrome		Slc5a3 (MGI:1858226)			
chr21	34364023	34371140	21q22.1	21q22.11		603796	"KCNE2, MIRP1, LQT6, ATFB4"	"Potassium voltage-gated channel, Isk-related family, member 2"	KCNE2	9992	ENSG00000159197		"Atrial fibrillation, familial, 4, 611493 (3); Long QT syndrome 6, 613693 (3), Autosomal dominant"	Kcne2 (MGI:1891123)			
chr21	34446687	34512274	21q22.1-q22.2	21q22.12		176261	"KCNE1, JLNS, LQT5, JLNS2"	"Potassium voltage-gated channel, Isk-related subfamily, member 1"	KCNE1	3753	ENSG00000180509		"Jervell and Lange-Nielsen syndrome 2, 612347 (3), Autosomal recessive; Long QT syndrome 5, 613695 (3), Autosomal dominant"				
chr21	34516441	34615141	21q22.1-q22.2	21q22.12		602917	"RCAN1, DSCR1, MCIP1, CSP1"	Regulator of calcineurin 1	RCAN1	1827	ENSG00000159200			Rcan1 (MGI:1890564)			
chr21	34668952	34718226	21q22.12	21q22.12		615321	"CLIC6, CLIC1L"	Chloride intracellular channel 6	CLIC6	54102	ENSG00000159212			Clic6 (MGI:2146607)			
chr21	34787800	35049333	21q22.3	21q22.12		151385	"RUNX1, CBFA2, AML1"	Runt-related transcription factor 1 (aml1 oncogene)	RUNX1	861	ENSG00000159216		"Leukemia, acute myeloid, 601626 (3), Autosomal dominant; Platelet disorder, familial, with associated myeloid malignancy, 601399 (3), Autosomal dominant"	Runx1 (MGI:99852)			
chr21	35720714	35720807	21q22.12	21q22.12		616090	MIR802	Micro RNA 802	MIR802	768219							
chr21	36069923	36073176	21q22.12	21q22.12		114830	CBR1	Carbonyl reductase 1	CBR1	873	ENSG00000159228			Cbr1 (MGI:88284)			
chr21	36134900	36146561	21q22.2	21q22.12		603608	CBR3	Carbonyl reductase 3	CBR3	874	ENSG00000159231			Cbr3 (MGI:1309992)			
chr21	36156780	36294273	21q22.2	21q22.12		604803	"DOPEY2, 21orf5, KIAA0933"	Dopey family member 2	DOPEY2	9980	ENSG00000142197			Dopey2 (MGI:1917278)			
chr21	36320188	36376645	21q22.12	21q22.12		610078	"MORC3, NXP2"	MORC family CW-type zinc finger 3	MORC3	23515	ENSG00000159256			Morc3 (MGI:2136841)			
chr21	36380144	36416826	21q22.2	21q22.12-q22.13		601245	CAF1A	"Chromatin assembly factor I, p60 subunit"	CHAF1B	8208	ENSG00000159259			Chaf1b (MGI:1314881)			
chr21	36400000	46709983	21q22.13-qter			609876	BMND6	Bone mineral density QTL 6		100188797		max lod at D21S1446	"[Bone mineral density QTL 6], 609876 (2)"				
chr21	36400000	38300000	21q22.13			609633	"MAFD3, BPEO"	Major affective disorder 3		100188792		max lod at D21S1252	"{Major affective disorder 3, early onset}, 609633 (2)"				
chr21	36460620	36576568	21q22.3	21q22.13		605608	"CLDN14, DFNB29"	Claudin 14	CLDN14	23562	ENSG00000159261		"Deafness, autosomal recessive 29, 614035 (3), Autosomal recessive"	Cldn14 (MGI:1860425)			
chr21	36699116	36750218	21q22.2	21q22.13		600892	SIM2	"Single-minded, Drosophila, homolog of, 2"	SIM2	6493	ENSG00000159263			Sim2 (MGI:98307)			
chr21	36748624	36990393	21q22.1	21q22.13		609018	"HLCS, HCS"	Holocarboxylase synthetase	HLCS	3141	ENSG00000159267		"Holocarboxylase synthetase deficiency, 253270 (3), Autosomal recessive"	Hlcs (MGI:894646)			
chr21	37006149	37019658	21q22.2	21q22.13		609892	"DSCR6, RIPPLY3"	Down syndrome critical region gene 6	RIPPLY3	53820	ENSG00000183145			Ripply3 (MGI:2181192)			
chr21	37065363	37073157	21q22.1-q22.2	21q22.13		605938	"PIGP, DSCR5, EIEE55"	"Phosphatidylinositol glycan, class P"	PIGP	51227	ENSG00000185808	mutation identified one EIEE55 family	"?Epileptic encephalopathy, early infantile, 55, 617599 (3), Autosomal recessive"	Pigp (MGI:1860433)			
chr21	37073183	37203117	21q22.2	21q22.13		602259	"TTC3, TPRD"	Tetratricopeptide repeat domain 3	TTC3	7267	ENSG00000182670			Ttc3 (MGI:1276539)			
chr21	37223419	37268107	21q22.2	21q22.13		605298	"DSCR3, DSCRA"	Down syndrome critical region gene 3	VPS26C	10311	ENSG00000157538			Dscr3 (MGI:1206040)			
chr21	37365572	37515375	21q22.1	21q22.13		600855	"DYRK1A, MNBH, MNB, MRD7"	"Dual specificity tyrosine-(Y)-phosphorylation regulated kinase-1A (\'minibrain\', Drosophila, homolog of)"	DYRK1A	1859	ENSG00000157540	?triplicate state responsible for mental defect in Down syndrome	"Mental retardation, autosomal dominant 7, 614104 (3), Autosomal dominant"	Dyrk1a (MGI:1330299)			
chr21	37624222	37916437	21q22.1	21q22.13		600877	"KCNJ6, GIRK2, KCNJ7, KPLBS"	"Potassium inwardly-rectifying channel, subfamily J, member 6"	KCNJ6	3763	ENSG00000157542		"Keppen-Lubinsky syndrome, 614098 (3), Autosomal dominant"	Kcnj6 (MGI:104781)			
chr21	38054010	38121359	21q22.2	21q22.13		604829	"DSCR4, DSCRB"	Down syndrome critical region gene 4	DSCR4	10281							
chr21	38121450	38156510	21q22.2	21q22.13		613396	"DSCR8, MMA1"	Down syndrome critical region gene 8	DSCR8	84677							
chr21	38229914	38303125	21q22.2	21q22.1-q22.2		602106	KCNJ15	"Potassium inwardly-rectifying channel, subfamily J, member 15"	KCNJ15	3772	ENSG00000157551			Kcnj15 (MGI:1310000)			
chr21	38367260	38661779	21q22.3	21q22.2		165080	ERG	"Erythroblastosis virus E26, avian, (v-ets) oncogene related"	ERG	2078	ENSG00000157554	"fused with EWS in Ewing sarcoma, with FUS in leukemia"		Erg (MGI:95415)			
chr21	38739020	38773476	21q22.2-q22.3	21q22.2		611723	C21orf24	Chromosome 21 open reading frame 24	LINC00114	400866							
chr21	38805306	38824954	21q22.3	21q22.2		164740	ETS2	Oncogene ETS-2	ETS2	2114	ENSG00000157557	proximal q22.3		Ets2 (MGI:95456)			
chr21	39175445	39183513	21q22.3	21q22.2		605296	"PSMG1, DSCR2, C21LRP"	"Proteasome (prosome, macropain) assembly chaperone 1"	PSMG1	8624	ENSG00000183527			Psmg1 (MGI:1860263)			
chr21	39184175	39321594	21q22.2-q22.3	21q22.2		617824	"BRWD1, WRD9, C21orf107"	Bromodomain and WD repeat domain-containing protein 1	BRWD1	54014	ENSG00000185658			Brwd1 (MGI:1890651)			
chr21	39342314	39349120	21q22.3	21q22.2		163920	"HMGN1, HMG14"	High-mobility group nucleosomal binding protein 1	HMGN1	3150	ENSG00000205581			Hmgn1 (MGI:96120)			
chr21	39380243	39428527	21q22.3	21q22.2		602915	"WRB, CHD5"	Tryptophan-rich basic protein	WRB	7485	ENSG00000182093			Wrb (MGI:2136882)			
chr21	39445864	39515505	21q22.3	21q22.2		602230	SH3GBR	SH3 domain binding glutamic acid-rich protein	SH3BGR	6450	ENSG00000185437						
chr21	39612939	39662888	21q22.3	21q22.2		604066	"B3GALT5, GLCT5"	"UDP-galactose:beta-N-acetylglucosamine beta-1,3-galactosyltransferase 5"	B3GALT5	10317	ENSG00000183778			B3galt5 (MGI:2136878)			
chr21	39632464	39802095	21q22.2	21q22.2		610638	JAM4	Junctional adhesion molecule 4	IGSF5	150084	ENSG00000183067			Igsf5 (MGI:1919308)			
chr21	39867420	39929396	21q22.3	21q22.2		601629	PCP4	Purkinje cell protein 4	PCP4	5121	ENSG00000183036			Pcp4 (MGI:97509)			
chr21	40010998	40847138	21q22.2-q22.3	21q22.2		602523	DSCAM	Down syndrome cell adhesion molecule	DSCAM	1826	ENSG00000171587			Dscam (MGI:1196281)			
chr21	41167800	41282533	21q22.3	21q22.2-q22.3		605668	"BACE2, ALP56, DRAP"	Beta-site amyloid beta A4 precursor protein-cleaving enzyme 2 (Down syndrome region aspartic protease)	BACE2	25825	ENSG00000182240			Bace2 (MGI:1860440)			
chr21	41175230	41185238	21q22.3	21q22.2		613770	PLAC4	Placenta-specific gene 4	PLAC4	191585							
chr21	41200000	46709983	21q22.3			190685	"DCR, DSCR"	Down syndrome chromosome region				many genes are involved in this phenotype	"Down syndrome, 190685 (4), Isolated cases"				
chr21	41200000	46709983	21q22.3			236100	HPE1	"Holoprosencephaly-1, alobar"	HPE1	3244			"Holoprosencephaly 1, 236100 (2), Autosomal dominant, Isolated cases"				
chr21	41304228	41357726	21q22	21q22.3		608617	FAM3B	"Family with sequence similarity 3, member B"	FAM3B	54097	ENSG00000183844			Fam3b (MGI:1270150)			
chr21	41361943	41408942	21q22.3	21q22.3		147890	MX2	Myxovirus (influenza) resistance-2	MX2	4600	ENSG00000183486						
chr21	41420328	41459213	21q22.3	21q22.3		147150	"MX1, MX, IFI78"	Myxovirus (influenza) resistance-1 (interferon induced protein p78)	MX1	4599	ENSG00000157601						
chr21	41464550	41508157	21q22.3	21q22.3		602060	TMPRSS2	"Transmembrane protease, serine 2"	TMPRSS2	7113	ENSG00000184012			Tmprss2 (MGI:1354381)			
chr21	41739368	41767088	21q22.3	21q22.3		605706	"RIPK4, NKRD3, DIK, PPS2"	Receptor-interacting serine-threonine kinase 4	RIPK4	54101	ENSG00000183421		"Popliteal pterygium syndrome, Bartsocas-Papas type, 263650 (3), Autosomal recessive"	Ripk4 (MGI:1919638)			
chr21	41798224	41879481	21q22.3	21q22.3		617692	"PRDM15, ZNF298"	PR domain-containing protein 15	PRDM15	63977	ENSG00000141956			Prdm15 (MGI:1930121)			
chr21	41885109	41953967	21q22.3	21q22.3		617581	"C2CD2, TMEM24L, C21orf25"	C2 calcium-dependent domain-containing protein 2	C2CD2	25966	ENSG00000157617			C2cd2 (MGI:1891883)			
chr21	41986830	42010417	21q22.3	21q22.3		616485	"ZBTB21, ZNF295, KIAA1227"	Zinc finger- and BTB domain-containing protein 21	ZBTB21	49854	ENSG00000173276			Zbtb21 (MGI:1927240)			
chr21	42062958	42142995	21q22.3	21q22.3		613859	UMODL1	Uromodulin-like 1	UMODL1	89766	ENSG00000177398			Umodl1 (MGI:1929785)			
chr21	42199688	42304386	21q22.3	21q22.3		603076	"ABCG1, ABC8, WHITE1"	"ATP-binding cassette, subfamily G, member 1 (white, Drosophila, homolog of)"	ABCG1	9619	ENSG00000160179			Abcg1 (MGI:107704)			
chr21	42311666	42315595	21q22.3	21q22.3		600633	"TFF3, ITF"	Trefoil factor 3 (intestinal)	TFF3	7033	ENSG00000160180			Tff3 (MGI:104638)			
chr21	42346356	42351098	21q22.3	21q22.3		182590	"TFF2, SML1"	Trefoil factor 2 (spasmolytic protein-1)	TFF2	7032	ENSG00000160181	within 230kb of BCEI		Tff2 (MGI:1306805)			
chr21	42362281	42366534	21q22.3	21q22.3		113710	"TFF1, BCEI"	"Trefoil factor 1 (breast cancer, estrogen-inducible sequence expressed in)"	TFF1	7031	ENSG00000160182			Tff1 (MGI:88135)			
chr21	42371886	42396845	21q22.3	21q22.3		605511	"TMPRSS3, ECHOS1, DFNB8, DFNB10"	"Transmembrane protease, serine 3"	TMPRSS3	64699	ENSG00000160183		"Deafness, autosomal recessive 8/10, 601072 (3), Autosomal recessive"	Tmprss3 (MGI:2155445)			
chr21	42403861	42447679	21q22.3	21q22.3		605736	UBASH3A	Ubiquitin-associated and SH3 domain-containing protein A	UBASH3A	53347	ENSG00000160185			Ubash3a (MGI:1926074)			
chr21	42472485	42496353	21q22.3	21q22.3		609314	"RSPH1, TSGA2, TSA2, CILD24"	"Radial spoke head 1, Chlamydomonas, homolog of"	RSPH1	89765	ENSG00000160188		"Ciliary dyskinesia, primary, 24, 615481 (3), Autosomal recessive"	Rsph1 (MGI:1194909)			
chr21	42499631	42581439	21q22.3	21q22.3		608094	"SLC37A1, G3PP"	"Solute carrier family 37 (glycerol-3-phosphate transporter), member 1"	SLC37A1	54020	ENSG00000160190			Slc37a1 (MGI:2446181)			
chr21	42653751	42775508	21q22.3	21q22.3		602973	"PDE9A, HSPDE9A2"	Phosphodiesterase 9A	PDE9A	5152	ENSG00000160191			Pde9a (MGI:1277179)			
chr21	42843074	42891694	21q22.3	21q22.3		605924	WDR4	WD repeat-containing protein 4	WDR4	10785	ENSG00000160193			Wdr4 (MGI:1889002)			
chr21	42893267	42911395	21q22.3	21q22.3		602184	NDUFV3	"NADH-ubiquinone oxidoreductase flavoprotein 3, 10kD"	NDUFV3	4731	ENSG00000160194			Ndufv3 (MGI:1890894)			
chr21	42974509	43033930	21q22.3	21q22.3		602100	PKNOX1	PBX/knotted 1 homeo box 1	PKNOX1	5316	ENSG00000160199			Pknox1 (MGI:1201409)			
chr21	43053189	43076860	21q22.3	21q22.3		613381	CBS	Cystathionine beta-synthase	CBS	875	ENSG00000160200	subtelomeric	"Homocystinuria, B6-responsive and nonresponsive types, 236200 (3), Autosomal recessive; Thrombosis, hyperhomocysteinemic, 236200 (3), Autosomal recessive"	Cbs (MGI:88285)			
chr21	43092955	43108290	21q22.3	21q22.3		191317	U2AF1	U2(RNU2) small nuclear RNA auxillary factor 1	U2AF1	7307	ENSG00000160201						
chr21	43169007	43172809	21q22.3	21q22.3		123580	"CRYAA, CRYA1, CTRCT9"	"Crystallin, alpha A"	CRYAA	1409	ENSG00000160202		"Cataract 9, multiple types, 604219 (3), Autosomal recessive, Autosomal dominant"	Cryaa (MGI:88515)			
chr21	43414489	43427131	21q22.3	21q22.3		605705	"SIK1, SNF1LK, MSK, EIEE30"	Salt-inducible kinase 1	SIK1	150094	ENSG00000142178		"Epileptic encephalopathy, early infantile, 30, 616341 (3), Autosomal dominant"				
chr21	43453986	43659498	21q22.3	21q22.3		604554	HSF2BP	Heat-shock transcription factor 2-binding protein	HSF2BP	11077	ENSG00000160207			Hsf2bp (MGI:1921627)			
chr21	43659550	43696078	21q22	21q22.3		610654	"RRP1B, KIAA0179, NNP1L"	"Ribosomal RNA-processing protein 1, S. cerevisiae, homolog of, B"	RRP1B	23076	ENSG00000160208			Rrp1b (MGI:1919712)			
chr21	43719096	43762306	21q22.3	21q22.3		179020	"PDXK, PNK, PKH"	Pyridoxal kinase	PDXK	8566	ENSG00000160209			Pdxk (MGI:1351869)			
chr21	43773664	43776374	21q22.3	21q22.3		601145	"CSTB, STFB, EPM1, PME, EPM1A, ULD"	Cystatin B (stefin B)	CSTB	1476	ENSG00000160213		"Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800 (3), Autosomal recessive"	Cstb (MGI:109514)			
chr21	43865159	43987593	21q22.3	21q22.3		614794	"AGPAT3, LPAAT3"	1-acylglycerol-3-phosphate O-acyltransferase 3	AGPAT3	56894	ENSG00000160216			Agpat3 (MGI:1336186)			
chr21	44012324	44106551	21q22.3	21q22.3		602103	"TMEM1, EHOC1"	Transmembrane protein 1	TRAPPC10	7109	ENSG00000160218	near PWP2H		Trappc10 (MGI:1336209)			
chr21	44107322	44131180	21q22.3	21q22.3		601475	"PWP2H, PWP2"	"PWP2 periodic tryptophan protein, yeast, homolog of"	PWP2	5822	ENSG00000241945						
chr21	44133611	44145722	21q22.3	21q22.3		601659	"ES1, HES1, GT335, C21orf33"	"ES1, zebrafish, protein, homolog of"	GATD3A	8209	ENSG00000160221			D10Jhu81e (MGI:1351861)			
chr21	44216978	44241003	21q22.3	21q22.3		605717	"ICOSLG, B7H2, GL50, B7RP1"	Inducible T-cell co-stimulator ligand	ICOSLG	23308	ENSG00000160223			Icosl (MGI:1354701)			
chr21	44246338	44262215	21q22.3	21q22.3		606588	DNMT3L	DNA methyltransferase 3-like protein	DNMT3L	29947	ENSG00000142182			Dnmt3l (MGI:1859287)			
chr21	44285837	44298218	21q22.3	21q22.3		607358	"AIRE, APECED, APS1"	Autoimmune regulator	AIRE	326	ENSG00000160224		"Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, 240300 (3), Autosomal recessive, Autosomal dominant"	Aire (MGI:1338803)			
chr21	44300033	44327380	21q22.3	21q22.3		171860	PFKL	"Phosphofructokinase, liver type"	PFKL	5211	ENSG00000141959		Hemolytic anemia due to phosphofructokinase deficiency (1)	Pfkl (MGI:97547)			
chr21	44328943	44339416	21q22.3	21q22.3		603191	"C21orf2, SMDAX, RDMS"	Chromosome 21 open reading frame 2	C21orf2	755	ENSG00000160226		"Retinal dystrophy with macular staphyloma, 617547 (3), Autosomal recessive; Spondylometaphyseal dysplasia, axial, 602271 (3), Autosomal recessive"	1810043G02Rik (MGI:1915134)			
chr21	44350111	44443080	21q22.3	21q22.3		603749	"TRPM2, TRPC7, KNP3"	"Transient receptor potential cation channel, subfamily M, member 2"	TRPM2	7226	ENSG00000142185			Trpm2 (MGI:1351901)			
chr21	44455485	44462195	21q22.3	21q22.3		617620	"LRRC3, C21orf102, C21orf30"	Leucine-rich repeat-containing protein 3	LRRC3	81543	ENSG00000160233			Lrrc3 (MGI:2447899)			
chr21	44497891	44711579	21q22.3	21q22.3		612920	"TSPEAR, C21orf29, DFNB98"	Thrombospondin-type laminin G domain and EAR repeats	TSPEAR	54084	ENSG00000175894	mutation identified in 1 DFNB98 family	"?Deafness, autosomal recessive 98, 614861 (3), Autosomal recessive"	Tspear (MGI:2671932)			
chr21	44768579	44801835	21q22.3	21q22.3		603124	"UBE2G2, UBC7"	Ubiquitin-conjugating enzyme E2G 2	UBE2G2	7327	ENSG00000184787			Ube2g2 (MGI:1343188)			
chr21	44805616	44818128	21q22.3	21q22.3		602231	"SUMO3, SMT3H1"	Small ubiquitin-like modifier 3	SUMO3	6612	ENSG00000184900			Sumo3 (MGI:1336201)			
chr21	44849584	44873902	21q22.3	21q22.3		603784	"PTTG1IP, C21orf1, C21orf3, PBF"	Pituitary tumor-transforming gene 1 protein-interacting protein	PTTG1IP	754	ENSG00000183255			Pttg1ip (MGI:2652132)			
chr21	44885948	44928872	21q22.3	21q22.3		600065	"ITGB2, CD18, LCAMB, LAD"	"Integrin, beta-2 (antigen CD18 (p95), lymphocyte function-associated antigen-1; macrophage antigen, beta polypeptide)"	ITGB2	3689	ENSG00000160255	"common subunit for CR3, LFA1, and P150,95"	"Leukocyte adhesion deficiency, 116920 (3), Autosomal recessive"	Itgb2 (MGI:96611)			
chr21	44989863	44994085	21q22.3	21q22.3		610259	"LINC00163, NCRNA00163, NLC1A"	Long intergenic nonprotein coding RNA 163	LINC00163	727699							
chr21	44999207	45004726	21q22.3	21q22.3		617191	"PICSAR, LINC00162, NLC1C"	p38-inhibited cutaneous squamous cell carcinoma-associated long intergenic noncoding RNA	PICSAR	378825							
chr21	45074577	45226562	21q22.3	21q22.3		601218	"ADARB1, RED1"	"Adenosine deaminase, RNA-specific, B1 (RED1, rat, homolog of)"	ADARB1	104	ENSG00000197381			Adarb1 (MGI:891999)			
chr21	45263927	45287913	21q22.3	21q22.3		610249	"POFUT2, C21Orf80, KIAA0958"	Protein O-fucosyltransferase 2	POFUT2	23275	ENSG00000186866			Pofut2 (MGI:1916863)			
chr21	45405136	45513719	21q22.3	21q22.3		120328	"COL18A1, KNO1"	"Collagen XVIII, alpha-1 polypeptide"	COL18A1	80781	ENSG00000182871		"Knobloch syndrome, type 1, 267750 (3), Autosomal recessive"	Col18a1 (MGI:88451)			
chr21	45502516	45563139	21q22.3	21q22.3		600424	"SLC19A1, FOLT"	"Solute carrier family 19 (folate transporter), member 1"	SLC19A1	6573	ENSG00000173638			Slc19a1 (MGI:103182)			
chr21	45643724	45942453	21q22.3	21q22.3		608502	PCBP3	Poly(rC)-binding protein 3	PCBP3	54039	ENSG00000183570			Pcbp3 (MGI:1890470)			
chr21	45981748	46005048	21q22.3	21q22.3		120220	"COL6A1, BTHLM1, UCHMD1"	"Collagen VI, alpha-1 polypeptide"	COL6A1	1291	ENSG00000142156		"Bethlem myopathy 1, 158810 (3), Autosomal recessive, Autosomal dominant; Ullrich congenital muscular dystrophy 1, 254090 (3), Autosomal recessive, Autosomal dominant"	Col6a1 (MGI:88459)			
chr21	46098070	46132848	21q22.3	21q22.3		120240	"COL6A2, BTHLM1, UCMD1"	"Collagen VI, alpha-2 polypeptide"	COL6A2	1292	ENSG00000142173	mutation identified in 1 MYSCL family	"Bethlem myopathy 1, 158810 (3), Autosomal recessive, Autosomal dominant; ?Myosclerosis, congenital, 255600 (3), Autosomal recessive; Ullrich congenital muscular dystrophy 1, 254090 (3), Autosomal recessive, Autosomal dominant"	Col6a2 (MGI:88460)			
chr21	46135980	46156481	21q22.3	21q22.3		606806	FTCD	Formiminotransferase cyclodeminase	FTCD	10841	ENSG00000160282		"Glutamate formiminotransferase deficiency, 229100 (3), Autosomal recessive"	Ftcd (MGI:1339962)			
chr21	46161147	46185162	21q22.3	21q22.3		612412	C21orf56	Chromosome 21 open reading frame 56	SPATC1L	84221	ENSG00000160284			Spatc1l (MGI:1923823)			
chr21	46188445	46228823	21q22.3	21q22.3		600909	"LSS, OSC, CTRCT44"	Lanosterol synthase	LSS	4047	ENSG00000160285		"Cataract 44, 616509 (3), Autosomal recessive"	Lss (MGI:1336155)			
chr21	46235124	46286296	21q22.3	21q22.3		603294	"MCM3AP, MAP80, GANP"	"Minichromosome maintenance 3-associated protein, 80-kD"	MCM3AP	8888	ENSG00000160294			Mcm3ap (MGI:1930089)			
chr21	46286055	46314187	21q22.3	21q22.3		617461	"YBEY, C21orf57"	YBEY metallopeptidase	YBEY	54059	ENSG00000182362			Ybey (MGI:2656825)			
chr21	46324121	46445768	21q22.3	21q22.3		605925	"PCNT, PCNT2, KEN, SCKL4, MOPD2"	Pericentrin	PCNT	5116	ENSG00000160299		"Microcephalic osteodysplastic primordial dwarfism, type II, 210720 (3), Autosomal recessive"				
chr21	46458941	46571225	21q22.3	21q22.3		607711	"DIP2, KIAA0184"	"Disco-interacting protein 2, Drosophila, homolog of"	DIP2A	23181	ENSG00000160305	previously mapped to Chr.2		Dip2a (MGI:2385920)			
chr21	46598617	46605242	21q22.2-q22.3	21q22.3		176990	S100B	"S100 calcium-binding protein, beta (neural)"	S100B	6285	ENSG00000160307			S100b (MGI:98217)			
chr21	46635155	46665684	21q22.3	21q22.3		601961	"HRMT1L1, PRMT2"	"HMT1 (hnRNP methyltransferase, S. cerevisiae)-like 1"	PRMT2	3275	ENSG00000160310			Prmt2 (MGI:1316652)			
chr21	0	46709983	Chr.21			109670	BAS	"Beta-adrenergic stimulation, response to"		8213							
chr21	0	46709983	Chr.21			143460	HTOR	5-hydroxytryptamine oxygenase regulator	HTOR	3349							
chr22	4300000	9400000	22p12			180454	RNR5	Ribosomal RNA-5	RNR5	6056							
chr22	11474776	11479642	22p	22p11.2		194547	ZNF73	Zinc finger protein-73 (Cos12)	ZNF73	105379427							
chr22	15000000	25500000	22q11			125520	ACF	Asymmetric crying facies (Cayler cardiofacial syndrome)		387569			"Cayler cardiofacial syndrome, 125520 (2), Autosomal dominant"				
chr22	15000000	25500000	22q11			115470	"CECR, CES"	Cat eye syndrome				partial tetrasomy of 22q11	"Cat eye syndrome, 115470 (4), Autosomal dominant"				
chr22	15000000	37200000	22q11-q12			151626	"LRE1, L1.2"	Line-1.2 retrotransposable element									
chr22	15690025	15721630	22q11.1	22q11.1		608913	"POTEH, POTE22, ACTBL1"	"POTE ankyrin domain family, member H"	POTEH	23784	ENSG00000198062						
chr22	16195708	16198039	22p	22q11.1		194546	ZNF72	Zinc finger protein-72 (Cos8)	ZNF72P	100287084							
chr22	16783411	16825411	22q11.1	22q11.1		611674	"XKR3, XTES, XRG3"	"X Kell blood group precursor-related family, member 3"	XKR3	150165	ENSG00000172967						
chr22	17084958	17115693	22q11.22-q11.23	22q11.1		605461	"IL17RA, IL17R, IMD51"	Interleukin 17 receptor A	IL17RA	23765	ENSG00000177663		"Immunodeficiency 51, 613953 (3), Autosomal recessive"	Il17ra (MGI:107399)			
chr22	17178789	17221853	22q11.2	22q11.1		607575	"CECR1, PAN, SNEDS"	"Cat eye syndrome chromosome region, candidate 1"	ADA2	51816	ENSG00000093072	mutation identified in 1 SNEDS family	"Polyarteritis nodosa, childhood-onset, 615688 (3), Autosomal recessive; ?Sneddon syndrome, 182410 (3), Autosomal recessive"				
chr22	17359948	17558154	22q11.2	22q11.1-q11.2		607576	"CECR2, KIAA1740"	"Cat eye syndrome chromosome region, candidate 2"	CECR2	27443	ENSG00000099954			Cecr2 (MGI:1923799)			
chr22	17400000	25500000	22q11.2			611867	"DEL22q11.2, C22DELq11.2"	"Chromosome 22q11.2 deletion syndrome, distal"					"Chromosome 22q11.2 deletion syndrome, distal, 611867 (4)"				
chr22	17400000	25500000	22q11.2			609029	DER22t11-22	Emanuel syndrome (supernumerary der(22)t(11;22) syndrome)					"Emanuel syndrome, 609029 (4), Inherited chromosomal imbalance"				
chr22	17400000	25500000	22q11.2			613700	DER22t8-22	Supernumerary der(22)t(8;22) syndrome					"Supernumerary der(22)t(8-22) syndrome, 613700 (4)"				
chr22	17400000	29200000	22q11.21-q12.1			608264	DFNB40	"Deafness, autosomal recessive 40"	DFNB40	379003			"Deafness, autosomal recessive 40, 608264 (2), Autosomal recessive"				
chr22	17400000	25500000	22q11.2			608363	DUP22q11.2	Chromosome 22q11.2 microduplication syndrome				contiguous gene microduplication syndrome	"Chromosome 22q11.2 microduplication syndrome, 608363 (4), Autosomal dominant, Isolated cases"				
chr22	17400000	25500000	22q11.2			600436	GSTT1	"Glutathione S-transferase, theta-1"	GSTT1	2952							
chr22	17400000	25500000	22q11.2			147230	IGLJ@	Immunoglobulin lambda light chain joining gene cluster		8217		nine J-C duplexes					
chr22	17400000	25500000	22q11.2			147240	IGLV@	Immunoglobulin lambda light chain variable gene cluster		3546		many genes					
chr22	17562469	17592255	22q11.2	22q11.21		609303	"SLC25A18, GC2"	"Solute carrier family 25 (mitochondrial carrier, glutamate), member 18"	SLC25A18	83733	ENSG00000182902			Slc25a18 (MGI:1919053)			
chr22	17592135	17628821	22q11.2	22q11.21		108746	"ATP6V1E1, ATP6E, ARCL2C"	"ATPase, H+ transporting, lysosomal, 31kD, V1 subunit E isoform 1"	ATP6V1E1	529	ENSG00000131100		"Cutis laxa, autosomal recessive, type IIC, 617402 (3), Autosomal recessive"	Atp6v1e1 (MGI:894326)			
chr22	17734139	17774664	22q11.2	22q11.21		601997	BID	BH3-interacting domain death agonist	BID	637	ENSG00000015475			Bid (MGI:108093)			
chr22	17787648	18024558	22q11.21	22q11.21		608882	"MICAL3, KIAA1364"	"Microtubule-associated monooxygenase, calponin and LIM domains-containing 3"	MICAL3	57553	ENSG00000243156			Mical3 (MGI:2442733)			
chr22	17980867	17980960	22q11.21	22q11.21		616205	MIR648	Micro RNA 648	MIR648	693233		in intron 1 of MICAL3					
chr22	18077919	18091030	22q11.21	22q11.21		608666	"PEX26, PBD7A, PBD7B"	Peroxisome biogenesis factor 26	PEX26	55670	ENSG00000215193		"Peroxisome biogenesis disorder 7A (Zellweger), 614872 (3), Autosomal recessive; Peroxisome biogenesis disorder 7B, 614873 (3), Autosomal recessive"	Pex26 (MGI:1921293)			
chr22	18110686	18131730	22q11	22q11.21		605742	"TUBA8, TUBAL2, CDCBM8"	"Tubulin, alpha 8"	TUBA8	51807	ENSG00000183785		"Cortical dysplasia, complex, with other brain malformations 8, 613180 (3), Autosomal recessive"	Tuba8 (MGI:1858225)			
chr22	18149854	18177396	22q11.2	22q11.21		607057	"USP18, UBP43, ISG43, PTORCH2"	Ubiquitin-specific protease 18	USP18	11274	ENSG00000184979		"Pseudo-TORCH syndrome 2, 617397 (3), Autosomal recessive"	Usp18 (MGI:1344364)			
chr22	18516334	18518164	22q11.2	22q11.21		612340	GGTLC3	"Gamma-glutamyltransferase, light chain 3"	GGTLC3	728226	ENSG00000274252						
chr22	18606123	18611918	22q11.21	22q11.21		612699	"RIMBP3, RIMBP3A, KIAA1666"	RIMS-binding protein 3	RIMBP3	85376	ENSG00000275793			Rimbp3 (MGI:2685449)			
chr22	18906222	18912087	22q11	22q11.21		601279	DGCR6	DiGeorge syndrome critical region 6	DGCR6	8214	ENSG00000183628						
chr22	18912773	18936552	22q11.2	22q11.21		606810	"PRODH, PRODH2, SCZD4"	Proline dehydrogenase (proline oxidase)	PRODH	5625	ENSG00000100033		"Hyperprolinemia, type I, 239500 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 4}, 600850 (3), Autosomal dominant"	Prodh (MGI:97770)			
chr22	19036281	19122453	22q11.2	22q11.21		600594	"DGCR2, IDD"	DiGeorge critical region gene 2 (integral membrane protein deleted in DiGeorge syndrome)	DGCR2	9993	ENSG00000070413			Dgcr2 (MGI:892866)			
chr22	19130278	19144725	22q11.2	22q11.21		601755	"ESS2, DGSI, DGCR14"	"Ess2 splicing factor, Xenopus, homolog of"	ESS2	8220	ENSG00000100056			Dgcr14 (MGI:107854)			
chr22	19130807	19132622	22q11.21	22q11.21		610710	"TSSK2, STK22B"	Testis-specific serine/threonine kinase 2	TSSK2	23617	ENSG00000206203			Tssk2 (MGI:1347559)			
chr22	19148990	19150282	22q11.21	22q11.21		601845	"GSC2, GSCL"	Goosecoid homeobox 2	GSC2	2928	ENSG00000063515			Gsc2 (MGI:892006)			
chr22	19175574	19178862	22q11	22q11.21		190315	"SLC25A1, SLC20A3, CTP, D2L2AD"	"Solute carrier family 25 (mitochondrial citrate transporter), member 1"	SLC25A1	6576	ENSG00000100075		"Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3), Autosomal recessive"				
chr22	19179472	19291715	22q11.2	22q11.21		601273	"CLTCL1, CLTD"	"Clathrin, heavy polypeptide-like 1"	CLTCL1	8218	ENSG00000070371						
chr22	19253120	19253468	22q11	22q11.21		601225	"DVL, DVL1"	"Dishevelled, Drosophila, homolog-like"	DVL1P1	8215							
chr22	19330700	19431695	22q11	22q11.21		600237	"HIRA, TUPLE1"	"Histone cell cycle regulation defective, S. cerevisiae, homolog of, A (Tup-like enhancer of split 1)"	HIRA	7290	ENSG00000100084	?role in CATCH22		Hira (MGI:99430)			
chr22	19431901	19436077	22q11.21	22q11.21		605089	"MRPL40, NLVCF, MRPL22"	Mitochondrial ribosomal protein L40	MRPL40	64976	ENSG00000185608			Mrpl40 (MGI:1332635)			
chr22	19449940	19479214	22q11.2	22q11.21		601754	UFD1L	Ubiquitin fusion degradation 1-like	UFD1	7353	ENSG00000070010	?role in CATCH22		Ufd1 (MGI:109353)			
chr22	19479293	19520611	22q11.2	22q11.21		603465	"CDC45L, CDC45L2, MGORS7"	"Cell division cycle 45, S. Cerevisiae, homolog-like"	CDC45	8318	ENSG00000093009		"Meier-Gorlin syndrome 7, 617063 (3), Autosomal recessive"	Cdc45 (MGI:1338073)			
chr22	19523023	19527544	22q11.2	22q11.21		602101	"CLDN5, TMVCF, AWAL"	Claudin-5 (transmembrane protein deleted in velocardiofacial syndrome)	CLDN5	7122	ENSG00000184113			Cldn5 (MGI:1276112)			
chr22	19714463	19723321	22q11.2	22q11.21		602724	"SEPT5, PNUTL1, CDCREL"	Septin 5	5-Sep	5413	ENSG00000184702	just 5' of GP1BB		Sept5 (MGI:1195461)			
chr22	19723542	19724773	22q11.2	22q11.21		138720	"GP1BB, BS, BDPLT1"	"Glycoprotein Ib, platelet, beta polypeptide"	GP1BB	2812	ENSG00000203618		"Bernard-Soulier syndrome, type B, 231200 (3), Autosomal recessive; Giant platelet disorder, isolated, 231200 (3), Autosomal recessive"	Gp1bb (MGI:107852)			
chr22	19756702	19783592	22q11.2	22q11.21		602054	"TBX1, DGS, CTHM, CAFS, TGA, DORV, VCFS, DGCR"	T-box 1	TBX1	6899	ENSG00000184058		"Conotruncal anomaly face syndrome, 217095 (3); DiGeorge syndrome, 188400 (3), Autosomal dominant; Tetralogy of Fallot, 187500 (3), Autosomal dominant; Velocardiofacial syndrome, 192430 (3), Autosomal dominant"	Tbx1 (MGI:98493)			
chr22	19788410	19854938	22q11.2	22q11.21		610778	"GNB1L, WDR14"	"Guanine nucleotide-binding protein, beta-1-like"	GNB1L	54584	ENSG00000185838			Gnb1l (MGI:1338057)			
chr22	19875517	19941991	22q11.2	22q11.21		606448	"TXNRD2, TRXR2, SELZ, GCCD5"	Thioredoxin reductase 2	TXNRD2	10587	ENSG00000184470	mutation identified in 1 GCCD5 family	"?Glucocorticoid deficiency 5, 617825 (3), Autosomal recessive"	Txnrd2 (MGI:1347023)			
chr22	19941739	19969974	22q11.2	22q11.21		116790	COMT	Catechol-O-methyltransferase	COMT	1312	ENSG00000093010		"{Panic disorder, susceptibility to}, 167870 (3), ?Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"	Comt (MGI:88470)			
chr22	19966726	20016801	22q11	22q11.21		602269	ARVCF	Armadillo repeat gene deleted in VCFS	ARVCF	421	ENSG00000099889	?role in VCFS		Arvcf (MGI:109620)			
chr22	20016999	20067163	22q11.2	22q11.21		616830	"TANGO2, C22orf25, MECRCN"	"Transport and golgi organization 2, Drosophila, homolog of"	TANGO2	128989	ENSG00000183597		"Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, 616878 (3), Autosomal recessive"	Tango2 (MGI:101825)			
chr22	20033138	20033219	22q11.21	22q11.21		615576	MIR185	Micro RNA 185	MIR185	406961		within first intron of C22orf25					
chr22	20080231	20111876	22q11.2	22q11.21		609030	DGCR8	DiGeorge syndrome critical region gene 8	DGCR8	54487	ENSG00000128191			Dgcr8 (MGI:2151114)			
chr22	20111865	20117294	22q11.21	22q11.21		611151	"TRMT2A, HTF9C"	"tRNA methyltransferase 2, S. cerevisiae, homolog of, A"	TRMT2A	27037	ENSG00000099899			Trmt2a (MGI:96270)			
chr22	20115937	20127356	22q11.21	22q11.21		601180	"RANBP1, HTF9A"	RAN-binding protein 1	RANBP1	5902	ENSG00000099901			Ranbp1 (MGI:96269)			
chr22	20131840	20148006	22q11.21	22q11.21		608784	"ZDHHC8, ZNF378, KIAA1292"	Zinc finger DHHC domain-containing protein 8	ZDHHC8	29801	ENSG00000099904			Zdhhc8 (MGI:1338012)			
chr22	20241414	20268292	22q11	22q11.21		605566	"RTN4R, NOGOR"	NOGO receptor (reticulon 4 receptor)	RTN4R	65078	ENSG00000040608		"{Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"	Rtn4r (MGI:2136886)			
chr22	20314237	20320104	22q11	22q11.21		609459	DGCR6L	DiGeorge syndrome critical region gene 6-like	DGCR6L	85359	ENSG00000128185						
chr22	20394114	20408462	22q11.2	22q11.21		194548	ZNF74	Zinc finger protein-74 (Cos52)	ZNF74	7625	ENSG00000185252						
chr22	20424583	20437858	22q11	22q11.21		613619	"SCARF2, SREC2, VDEGS"	"Scavenger receptor class F, member 2"	SCARF2	91179	ENSG00000244486		"Van den Ende-Gupta syndrome, 600920 (3), Autosomal recessive"	Scarf2 (MGI:1858430)			
chr22	20507541	20587631	22q11.2	22q11.21		607372	"MED15, PCQAP, TIG1, ARC105"	Mediator complex subunit 15	MED15	51586	ENSG00000099917						
chr22	20707690	20858811	22q11.21	22q11.21		600286	"PI4KA, PIK4CA, PMGYCHA"	"Phosphatidylinositol 4-kinase, catalytic, alpha"	PI4KA	5297	ENSG00000241973		"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, 616531 (3), Autosomal recessive"	Pi4ka (MGI:2448506)			
chr22	20774094	20787719	22q11	22q11.21		142360	"HCF2, HC2, SERPIND1, THPH10"	Heparin cofactor II	SERPIND1	3053	ENSG00000099937	proximal to BCR	"Thrombophilia due to heparin cofactor II deficiency, 612356 (3), Autosomal dominant"	Serpind1 (MGI:96051)			
chr22	20859003	20891213	22q11.2	22q11.21		604202	"SNAP29, CEDNIK"	"Synaptosomal-associated protein, 29kD"	SNAP29	9342	ENSG00000099940		"Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome, 609528 (3), Autosomal recessive"	Snap29 (MGI:1914724)			
chr22	20917406	20953748	22q11	22q11.21		602007	CRKL	v-crk avian sarcoma virus CT10 oncogene homolog-like	CRKL	1399	ENSG00000099942			Crkl (MGI:104686)			
chr22	20965129	20981359	22q11.21	22q11.21		617298	"AIFM3, AIFL"	"Apoptosis-inducing factor, mitochondria-associated, 3"	AIFM3	150209	ENSG00000183773			Aifm3 (MGI:1919418)			
chr22	20982268	20999036	22q11.1-q11.2	22q11.21		600574	"LZTR1, SWNTS2, NS10"	Leucine-zipper-like regulator-1	LZTR1	8216	ENSG00000099949		"Noonan syndrome 10, 616564 (3), Autosomal dominant; {Schwannomatosis-2, susceptibility to}, 615670 (3), Autosomal dominant"	Lztr1 (MGI:1914113)			
chr22	21009698	21028012	22q11	22q11.21		608077	"P2RXL1, P2XM, P2X6"	Purinergic receptor P2X-like 1	P2RX6	9127	ENSG00000099957			P2rx6 (MGI:1337113)			
chr22	21028717	21032557	22q11.2	22q11.21		603752	"SLC7A4, CAT4"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 4"	SLC7A4	6545	ENSG00000099960			Slc7a4 (MGI:2146512)			
chr22	21207971	21283022	22q11.1	22q11.21		137181	GGT2	Gamma-glutamyltransferase-2	GGT2	728441	ENSG00000133475		"[Gamma-glutamyltransferase, familial high serum], 137181 (2)"				
chr22	21383750	21389168	22q11.21	22q11.21		612700	RIMBP3B	RIMS-binding protein 3B	RIMBP3B	440804	ENSG00000274600			Rimbp3 (MGI:2685449)			
chr22	21417402	21451462	22q11.2	22q11.21		607712	"HIC2, HRG22, KIAA1020"	Hypermethylated in cancer 2	HIC2	23119	ENSG00000169635			Hic2 (MGI:1929869)			
chr22	21545665	21551460	22q11.21	22q11.21		612701	RIMBP3C	RIMS-binding protein 3C	RIMBP3C	150221	ENSG00000183246			Rimbp3 (MGI:2685449)			
chr22	21549446	21624033	22q11.2-q13.1	22q11.21		603721	"UBE2L3, UBCH7"	Ubiquitin-conjugating enzyme E2L 3	UBE2L3	7332	ENSG00000185651	pseudogenes on 12q12 and 19q13.1-q13.2		Ube2l3 (MGI:109240)			
chr22	21642252	21644298	22q11.2	22q11.21		607551	SDF2L1	Stromal cell-derived factor 2-like 1	SDF2L1	23753	ENSG00000128228			Sdf2l1 (MGI:2149842)			
chr22	21653303	21653384	22q11.21-q11.22	22q11.21		613682	"MIR130B, MIRN130B"	Micro RNA 130B	MIR130B	406920							
chr22	21665983	21698282	22q11.21	22q11.21		607588	"PPIL2, CYP60"	Peptidyl-prolyl isomerase-like 2	PPIL2	23759	ENSG00000100023			Ppil2 (MGI:2447857)			
chr22	21697535	21735833	22q11.2	22q11.21-q11.22		608082	YPEL1	Yippee-like 1	YPEL1	29799	ENSG00000100027	pseudogene on 9p24.3		Ypel1 (MGI:1913303)			
chr22	21759656	21867679	22q11.2	22q11.22		176948	"MAPK1, PRKM1, ERK2"	Mitogen-activated protein kinase 1	MAPK1	5594	ENSG00000100030			Mapk1 (MGI:1346858)			
chr22	21954358	21982842	22q11	22q11.22		603582	TOP3B	"Topoisomerase, DNA, III, beta"	TOP3B	8940	ENSG00000100038			Top3b (MGI:1333803)			
chr22	22244779	22245514	22q11.2	22q11.22		605141	"VPREB1, IGI, VPREB"	Pre-B lymphocyte gene 1	VPREB1	7441	ENSG00000169575			"Vpreb1,Vpreb2 (MGI:98936,MGI:98937)"			
chr22	22547695	22559360	22q11.22	22q11.22		606021	"PRAME, MAPE, OIP4"	Preferentially expressed antigen in melanoma	PRAME	23532	ENSG00000185686						
chr22	22644619	22647897	22q11.2	22q11.22		612339	"GGTLC2, GGTL4"	"Gamma-glutamyltransferase, light chain 2"	GGTLC2	91227	ENSG00000100121						
chr22	22822775	22822870	22q11.22	22q11.22		615379	MIR650	Micro RNA 650	MIR650	723778							
chr22	22895374	22895693	22q11.2	22q11.22		147220	"IGLC1, IGLC"	Constant region of lambda light chains	IGLC1	3537		several genes					
chr22	23059407	23180047	22q11.2	22q11.22-q11.23		605663	"RSPH14, RTDR1"	"Radial spoke head 14, Chlamydomonas, homolog of"	RSPH14	27156	ENSG00000100218			Rsph14 (MGI:1918486)			
chr22	23070348	23125036	22q11.2	22q11.22-q11.23		139160	GNAZ	"Guanine nucleotide-binding protein (G protein), alpha z polypeptide"	GNAZ	2781	ENSG00000128266			Gnaz (MGI:95780)			
chr22	23145297	23169284	22q11.2	22q11.23		605662	RAB36	"Ras family, member 36"	RAB36	9609	ENSG00000100228			Rab36 (MGI:1924127)			
chr22	23180364	23318036	22q11.21	22q11.23		151410	"BCR, CML, PHL, ALL"	Breakpoint cluster region	BCR	613	ENSG00000186716	Ph1=t(9;22) (q34.1;q11.21); fused with ABL in CML	"Leukemia, acute lymphocytic, somatic, 613065 (3); Leukemia, chronic myeloid, somatic, 608232 (3)"	Bcr (MGI:88141)			
chr22	23573124	23580547	22q11.21	22q11.23		146770	"IGLL1, IGO, IGL5, VPREB2, AGM2"	Immunoglobulin lambda-like polypeptide 1 (immunoglobulin omega peptide)	IGLL1	3543	ENSG00000128322	between BCR2 and BCR4; distal to IGLC	"Agammaglobulinemia 2, 613500 (3), Autosomal recessive"	Igll1 (MGI:96529)			
chr22	23690860	23699175	22q11.2	22q11.23		612214	"RGL4, RGR"	Ral guanine nucleotide dissociation stimulator-like 4	RGL4	266747	ENSG00000159496						
chr22	23741583	23751091	22q11.2	22q11.23		194544	ZNF70	Zinc finger protein-70 (Cos17)	ZNF70	7621	ENSG00000187792						
chr22	23752742	23754442	22q11	22q11.23		605017	VPREB3	Pre-B-lymphocyte gene 3	VPREB3	29802	ENSG00000128218			Vpreb3 (MGI:98938)			
chr22	23765833	23767971	22q11.23	22q11.23		615903	"CHCHD10, FTDALS2, SMAJ, IMMD"	Coiled-coil-helix-coiled-coil-helix domain-containing protein 10	CHCHD10	400916	ENSG00000250479	mutation identified in 1 IMMD family	"Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 (3), Autosomal dominant; ?Myopathy, isolated mitochondrial, autosomal dominant, 616209 (3), Autosomal dominant; Spinal muscular atrophy, Jokela type, 615048 (3), Autosomal dominant"	Chchd10 (MGI:2143558)			
chr22	23772818	23784315	22q11.2	22q11.23		185261	"MMP11, STMY3"	Matrix metalloproteinase 11 (stromelysin 3)	MMP11	4320	ENSG00000099953			Mmp11 (MGI:97008)			
chr22	23786930	23834517	22q11	22q11.23		601607	"SMARCB1, SNF5, INI1, RDT, RTPS1, MRD15, SWNTS1, CSS3"	"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1"	SMARCB1	6598	ENSG00000099956		"Coffin-Siris syndrome 3, 614608 (3), Autosomal dominant; {Rhabdoid tumor predisposition syndrome 1}, 609322 (3), Autosomal dominant; Rhabdoid tumors, somatic, 609322 (3); {Schwannomatosis-1, susceptibility to}, 162091 (3), Autosomal dominant"	Smarcb1 (MGI:1328366)			
chr22	23834497	23839347	22q11.23	22q11.23		610305	DERL3	"DER1-like domain family, member 3"	DERL3	91319	ENSG00000099958			Derl3 (MGI:1917627)			
chr22	23856702	23886111	22q11.2	22q11.23		610367	"SLC2A11, GLUT11"	"Solute carrier family 2 (facilitated glucose transporter), member 11"	SLC2A11	66035	ENSG00000133460						
chr22	23894377	23895221	22q11.2	22q11.23		153620	MIF	Macrophage migration inhibitory factor	MIF	4282	ENSG00000240972	previously assigned to chr.19	"{Rheumatoid arthritis, systemic juvenile, susceptibility to}, 604302 (3)"	Mif (MGI:96982)			
chr22	23971364	23979827	22q11.2	22q11.23		602750	DDT	D-dopachrome tautomerase	DDT	1652	ENSG00000099977			Ddt (MGI:1298381)			
chr22	23980027	23983914	22q11.2	22q11.23		600437	GSTT2	Glutathione S-transferase theta-2	GSTT2	2953	ENSG00000099984			Gstt2 (MGI:106188)			
chr22	24011191	24178627	22q11.2	22q11.23		604251	"CABIN1, CAIN"	Calcineurin-binding protein 1	CABIN1	23523	ENSG00000099991			Cabin1 (MGI:1298375)			
chr22	24181475	24189105	22q11.23	22q11.23		615825	SUSD2	Sushi domain-containing protein 2	SUSD2	56241	ENSG00000099994			Susd2 (MGI:1918983)			
chr22	24219653	24245141	22q11.2	22q11.23		137168	GGT5	Gamma-glutamyltransferase 5	GGT5	2687	ENSG00000099998			Ggt5 (MGI:1346063)			
chr22	24270816	24417739	22q11.23	22q11.23		614140	"SPECC1L, KIAA0376, OBLFC1, GBBB2"	Sperm antigen with calponin homology and coiled-coil domains 1-like	SPECC1L	23384	ENSG00000100014	mutation identified in 1 OBLFC1 patient	"?Facial clefting, oblique, 1, 600251 (3), Autosomal dominant; Opitz GBBB syndrome, type II, 145410 (3), Autosomal dominant"	Specc1l (MGI:1921642)			
chr22	24423596	24442359	22q11.2	22q11.23		102776	ADORA2A	Adenosine A2a receptor	ADORA2A	135	ENSG00000128271	incorrectly assigned to 11q		Adora2a (MGI:99402)			
chr22	24495059	24528680	22q11.2	22q11.23		606673	"UPB1, BUP1"	Beta-ureidopropionase	UPB1	51733	ENSG00000100024		"Beta-ureidopropionase deficiency, 613161 (3), Autosomal recessive"	Upb1 (MGI:2143535)			
chr22	24555649	24574963	22q11.23	22q11.23		601062	SNRPD3	Small nuclear ribonucleoprotein polypeptide D3	SNRPD3	6634	ENSG00000100028			Snrpd3 (MGI:1914582)			
chr22	24583749	24629004	22q11.2	22q11.23		612346	"GGT1, GGT"	Gamma-glutamyltransferase 1	GGT1	2678	ENSG00000100031		"Glutathioninuria, 231950 (1), Autosomal recessive"	Ggt1 (MGI:95706)			
chr22	24719033	24774719	22q11.2	22q11.23		610314	PIWIL3	PIWI-like 3	PIWIL3	440822	ENSG00000184571						
chr22	25194243	25207616	22q11.2-q12.2	22q11.23		123630	"CRYBB3, CRYB3, CATCN2, CTRCT22"	"Crystallin, beta-B3"	CRYBB3	1417	ENSG00000100053		"Cataract 22, 609741 (3), Autosomal recessive, Autosomal dominant"	Crybb3 (MGI:102717)			
chr22	25211659	25231868	22q11.2-q12.2	22q11.23		123620	"CRYBB2, CRYB2, CTRCT3, CCA2"	"Crystallin, beta-B2"	CRYBB2	1415	ENSG00000244752	2nd CRYB2 gene in same region	"Cataract 3, multiple types, 601547 (3), Autosomal dominant"	Crybb2 (MGI:88519)			
chr22	25500000	37200000	22q12			613106	BRV2	"Vertigo, benign recurrent, 2"		100313948			"Vertigo, benign recurrent, 2, 613106 (2)"				
chr22	25500000	50818468	22q12-q13			603116	CDAGS	"Craniosynostosis, anal anomalies, and porokeratosis syndrome"		574043			"CDAGS syndrome, 603116 (2), Autosomal recessive"				
chr22	25500000	50818468	22q12-q13			613284	HCHGQ3	Hematocrit/hemoglobin quantitative trait locus 3		100381206		associated with rs855791	"[Hematocrit/hemoglobin quantitative trait locus 3], 613284 (2)"				
chr22	25500000	31800000	22q12.1-q12.2			606960	ITS	Insulinoma tumor suppressor gene locus		282551			Insulinoma (1)				
chr22	25500000	37200000	22q12			608207	KAZA1	"Kala-azar (visceral leishmaniasis), susceptibility to, 1"		387582			"{Kala-azar, susceptibility to, 1}, 608207 (2)"				
chr22	25500000	37200000	22q12			611004	SQTL2	Smoking as a quantitative trait locus 2		100188828		max lod at D22S315	"{Smoking as a quantitative trait locus 2}, 611004 (2)"				
chr22	25564893	25729293	22q11	22q12.1		109636	"ADRBK2, BARK2, GRK3"	"Adrenergic, beta, receptor kinase-2"	GRK3	157	ENSG00000100077			Grk3 (MGI:87941)			
chr22	25742132	26063846	22q12.1	22q12.1		607295	"MYO18B, KFS4"	Myosin XVIIIB	MYO18B	84700	ENSG00000133454		"Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 (3), Autosomal recessive"	Myo18b (MGI:1921626)			
chr22	26169473	26383596	22q12.1	22q12.1		607021	SEZ6L	Seizure-related 6-like	SEZ6L	23544	ENSG00000100095			Sez6l (MGI:1935121)			
chr22	26443108	26483862	22q11.2-q12.2	22q12.1		606682	HPS4	HPS gene 4	HPS4	89781	ENSG00000100099		"Hermansky-Pudlak syndrome 4, 614073 (3), Autosomal recessive"	Hps4 (MGI:2177742)			
chr22	26483866	26494619	22q12.1	22q12.1		602254	SRRD	SRR1 domain-containing protein	SRRD	402055	ENSG00000100104			Srrd (MGI:1917368)			
chr22	26491239	26513590	22q12.1	22q12.1		612747	"TFIP11, TIP39, NTR1"	Tuftelin-interacting protein 11	TFIP11	24144	ENSG00000100109			Tfip11 (MGI:1930075)			
chr22	26524081	26590140	22q12.1	22q12.1		603126	TPST2	Tyrosylprotein phosphotransferase 2	TPST2	8459	ENSG00000128294			Tpst2 (MGI:1309516)			
chr22	26599277	26618103	22q11.2-q12.1	22q12.1		600929	"CRYBB1, CATCN3, CTRCT17"	"Crystallin, beta B1"	CRYBB1	1414	ENSG00000100122		"Cataract 17, multiple types, 611544 (3), Autosomal recessive, Autosomal dominant"	Crybb1 (MGI:104992)			
chr22	26607981	26630671	22q11.2-q13.1	22q12.1		123631	"CRYBA4, CTRCT23"	"Crystallin, beta polypeptide A4"	CRYBA4	1413	ENSG00000196431		"Cataract 23, 610425 (3)"	Cryba4 (MGI:102716)			
chr22	26657481	26676477	22q12.1	22q12.1		611082	"MIAT, C22orf35"	MIAT gene	MIAT	440823			"{Myocardial infarction, susceptibility to}, 608446 (3)"				
chr22	27748276	27801497	22q12.3-qter	22q12.1		156100	"MN1, MGCR"	Meningioma chromosome region	MN1	4330	ENSG00000169184	fused with TEL in AML	"Meningioma, 607174 (3), Autosomal dominant"	Mn1 (MGI:1261813)			
chr22	27851668	27919305	22q12.1	22q12.1		606876	PITPNB	"Phosphatidylinositol transfer protein, beta"	PITPNB	23760	ENSG00000180957			Pitpnb (MGI:1927542)			
chr22	27978013	28679864	22q12.1	22q12.1		615098	"TTC28, TPRBK, KIAA1043"	Tetratricopeptide repeat domain-containing protein 28	TTC28	23331	ENSG00000100154			Ttc28 (MGI:2140873)			
chr22	28687742	28741865	22q12.1	22q12.1		604373	"CHEK2, RAD53, CHK2, CDS1, LFS2"	"Checkpoint kinase 2, S. pombe, homolog of (RAD53, S. cerevisiae, homolog of)"	CHEK2	11200	ENSG00000183765		"{Breast and colorectal cancer, susceptibility to} (3); {Breast cancer, susceptibility to}, 114480 (3), Autosomal dominant; Li-Fraumeni syndrome, 609265 (3); Osteosarcoma, somatic, 259500 (3); {Prostate cancer, familial, susceptibility to}, 176807 (3), Autosomal dominant"	Chek2 (MGI:1355321)			
chr22	28741991	28757517	22q11-q12	22q12.1		608142	"HSC20, HSCB, JAC1"	"HSC20, E. coli, homolog of"	HSCB	150274	ENSG00000100209			Hscb (MGI:2141135)			
chr22	28794559	28800571	22q12	22q12.1		194355	"XBP1, XBP2"	X-box-binding protein-1	XBP1	7494	ENSG00000100219	pseudogene on chr.5	"{Major affective disorder-7, susceptibility to}, 612371 (3)"	Xbp1 (MGI:98970)			
chr22	28800656	29057487	22q12.1	22q12.1		612062	"ZNRF3, KIAA1133"	Zinc finger and ring finger protein 3	ZNRF3	84133	ENSG00000183579			Znrf3 (MGI:3039616)			
chr22	29073077	29168332	22q12.1	22q12.1		609898	"KREMEN1, KRM1, ECTD13"	Kringle domain-containing transmembrane protein 1	KREMEN1	83999	ENSG00000183762		"Ectodermal dysplasia 13, hair/tooth type, 617392 (3), Autosomal recessive"	Kremen1 (MGI:1933988)			
chr22	29268008	29300524	22q12	22q12.2		133450	"EWSR1, EWS"	Ewing sarcoma breakpoint region-1	EWSR1	2130	ENSG00000182944	t(11;22)(q24;q12); t(21;22)(q22;q12)	"Ewing sarcoma, 612219 (3); Neuroepithelioma, 612219 (3)"				
chr22	29306649	29312788	22q12	22q12.2		602128	"GAS2L1, GAR22"	Growth arrest-specific 2 like 1	GAS2L1	10634	ENSG00000185340			Gas2l1 (MGI:1926176)			
chr22	29312932	29319617	22q12	22q12.2		602220	"RASL10A, RRP22"	"Ras-like, family 10, member A"	RASL10A	10633	ENSG00000100276			Rasl10a (MGI:1922918)			
chr22	29327679	29388582	22q12	22q12.2		600157	"AP1B1, ADTB1, BAM22, CLAPB2"	"Adaptor-related protein complex 1, beta 1 subunit (adaptin, beta)"	AP1B1	162	ENSG00000100280			Ap1b1 (MGI:1096368)			
chr22	29403030	29442489	22q12-q13	22q12.2		605968	RFPL1	RET finger protein-like 1	RFPL1	5988	ENSG00000128250						
chr22	29437014	29442128	22q12-q13	22q12.2		605972	RFPL1S	"Ret finger protein-like 1, antisense"	RFPL1S	10740							
chr22	29480191	29491289	22q12.2	22q12.2		162230	"NEFH, CMT2CC"	"Neurofilament, heavy polypeptide"	NEFH	4744	ENSG00000100285	mutation identified in 1 family with ALS susceptibility	"?{Amyotrophic lateral sclerosis, susceptibility to}, 105400 (3), Autosomal recessive, Autosomal dominant; Charcot-Marie-Tooth disease, axonal, type 2CC, 616924 (3), Autosomal dominant"	Nefh (MGI:97309)			
chr22	29508166	29553759	22q12	22q12.2		612733	"THOC5, FMIP"	THO complex 5	THOC5	8563	ENSG00000100296			Thoc5 (MGI:1351333)			
chr22	29554807	29581336	22q12	22q12.2		603249	NIPSNAP1	4-nitrophenylphosphatase domain and nonneuronal SNAP25-like 1	NIPSNAP1	8508	ENSG00000184117			Nipsnap1 (MGI:1278344)			
chr22	29603555	29698599	22q12.2	22q12.2		607379	NF2	Merlin	NF2	4771	ENSG00000186575	loss of heterozygosity	"Meningioma, NF2-related, somatic, 607174 (3); Neurofibromatosis, type 2, 101000 (3), Autosomal dominant; Schwannomatosis, somatic, 162091 (3)"	Nf2 (MGI:97307)			
chr22	29767368	29770412	22cen-q12	22q12.2		610843	UCRC	"Ubiquinol-cytochrome C reductase complex, 7.2kD subunit"	UQCR10	29796	ENSG00000184076			Uqcr10 (MGI:1913402)			
chr22	29788607	29838303	22q12.2	22q12.2		614216	"ASCC2, p100"	"Activating signal cointegrator 1 complex, subunit 2"	ASCC2	84164	ENSG00000100325			Ascc2 (MGI:1922702)			
chr22	29883164	30030867	22q12	22q12.2		603558	MTMR3	Myotubularin-related protein 3	MTMR3	8897	ENSG00000100330			Mtmr3 (MGI:1921552)			
chr22	30240446	30257486	22q12.1-q12.2	22q12.2		159540	"LIF, HILDA"	Leukemia inhibitory factor (cholinergic differentiation factor)	LIF	3976	ENSG00000128342	distal to ES		Lif (MGI:96787)			
chr22	30262827	30266842	22q12.1-q12.2	22q12.2		165095	OSM	Oncostatin M	OSM	5008	ENSG00000099985	10kb from LIF		Osm (MGI:104749)			
chr22	30285117	30289626	22q12.2	22q12.2		617034	"GATSL3, CASTOR1"	GATS protein-like 3	CASTOR1	652968	ENSG00000239282			Gatsl3 (MGI:1919212)			
chr22	30291989	30326965	22q12.1-qter	22q12.2		610020	"TBC1D10A, EPI64"	"TBC1 domain family, member 10A"	TBC1D10A	83874	ENSG00000099992			Tbc1d10a (MGI:2144164)			
chr22	30331987	30356946	22q12.2	22q12.2		605595	"SF3A1, SF3A120, SAP114, PRP21"	"Splicing factor 3A, subunit 1"	SF3A1	10291	ENSG00000099995			Sf3a1 (MGI:1914715)			
chr22	30396940	30425302	22q12.1-qter	22q12.2		607558	"SEC14L2, TAP, KIAA1186"	Sec14-like 2	SEC14L2	23541	ENSG00000100003			Sec14l2 (MGI:1915065)			
chr22	30425622	30429053	22q12.2	22q12.2		610235	MTFP1	Mitochondrial fission process 1	MTFP1	51537	ENSG00000242114			Mtfp1 (MGI:1916686)			
chr22	30447958	30472046	22q12	22q12.2		612824	"SEC14L3, TAP2"	Sec14-like 3	SEC14L3	266629	ENSG00000100012			Sec14l3 (MGI:3617848)			
chr22	30488149	30505710	22q12	22q12.2		612825	"SEC14L4, TAP3"	Sec14-like 4	SEC14L4	284904	ENSG00000133488			Sec14l4 (MGI:2144095)			
chr22	30554634	30574587	22q12.2	22q12.2		602300	"GAL3ST1, CST"	Galactose-3-O-sulfotransferase 1	GAL3ST1	9514	ENSG00000128242			Gal3st1 (MGI:1858277)			
chr22	30576624	30607012	22q12.1	22q12.2		605819	"PES1, PES"	"Pescadillo, zebrafish, homolog of, 1"	PES1	23481	ENSG00000100029			Pes1 (MGI:1890613)			
chr22	30607082	30627059	22q11.2-qter	22q12.2		613441	"TCN2, TC2"	Transcobalamin II	TCN2	6948	ENSG00000185339	linked to P1	"Transcobalamin II deficiency, 275350 (3), Autosomal recessive"	Tcn2 (MGI:98534)			
chr22	30693781	30907823	22q12	22q12.2		606729	"OSBP2, ORP4, KIAA1664"	Oxysterol-binding protein 2	OSBP2	23762	ENSG00000184792			Osbp2 (MGI:1921559)			
chr22	30925129	30968286	22q12.2	22q12.2		616661	"MORC2, ZCW3, ZCWCC1, KIAA0852, CMT2Z"	MORC family CW-type zinc finger protein 2	MORC2	22880	ENSG00000133422		"Charcot-Marie-Tooth disease, axonal, type 2Z, 616688 (3), Autosomal dominant"	Morc2a (MGI:1921772)			
chr22	30969210	30979394	22q12.2	22q12.2		614971	TUG1	"Taurine-upregulated gene 1, noncoding"	TUG1	55000							
chr22	31081295	31104623	22q12.3	22q12.2		602127	SMTN	Smoothelin	SMTN	6525	ENSG00000183963			Smtn (MGI:1354727)			
chr22	31104771	31107586	22q12.2	22q12.2		610918	"SELENOM, SELM, SEPM"	Selenoprotein M	SELENOM	140606	ENSG00000198832			Selenom (MGI:2149786)			
chr22	31107735	31134696	22q11.2-q13.2	22q12.2		606481	"INPP5J, PIB5PA, PIPP"	Inositol polyphosphate-5-phosphatase J	INPP5J	27124	ENSG00000185133			Inpp5j (MGI:2158663)			
chr22	31134806	31140606	22q11.2-q13.2	22q12.2		611651	"PLA2G3, SPLA2III"	"Phospholipase A2, group III"	PLA2G3	50487	ENSG00000100078			Pla2g3 (MGI:2444945)			
chr22	31212263	31280079	22q12.2	22q12.2		601988	LIMK2	LIM domain kinase 2	LIMK2	3985	ENSG00000182541			Limk2 (MGI:1197517)			
chr22	31325803	31346262	22q12	22q12.2		605165	"ZNF278, PATZ, MAZR"	Zinc finger protein-278	PATZ1	23598	ENSG00000100105			Patz1 (MGI:1891832)			
chr22	31434647	31489949	22q11.2	22q12.2		607445	EIF4ENIF1	Eukaryotic translation initiation factor 4E nuclear import factor 1	EIF4ENIF1	56478	ENSG00000184708			Eif4enif1 (MGI:1921453)			
chr22	31496138	31618553	22q12.2	22q12.2		612765	"SFI1, KIAA0542"	"SFI1, yeast, homolog of"	SFI1	9814	ENSG00000198089			Sfi1 (MGI:1926137)			
chr22	31618490	31662563	22q12	22q12.2		612770	"PISD, PSD, PSSC"	Phosphatidylserine decarboxylase	PISD	23761	ENSG00000241878			Pisd (MGI:2445114)			
chr22	31753950	31907033	22q12.2-q12.3	22q12.2-q12.3		614191	"DEPDC5, KIAA0645, FFEVF1"	DEP domain-containing protein 5	DEPDC5	9681	ENSG00000100150		"Epilepsy, familial focal, with variable foci 1, 604364 (3), Autosomal dominant"	Depdc5 (MGI:2141101)			
chr22	31800000	37200000	22q12.3			609558	HPC6	"Prostate cancer, hereditary, 6"		100188789		between D22S1265 and D22S277	"{Prostate cancer, susceptibility to}, 176807 (2), Autosomal dominant"				
chr22	31800000	40600000	22q12.3-q13.1			613689	MDNS	Mammary-digital-nail syndrome		100529148		"max lod at D22S277, D22S1142, D22S683, D22S283"	"Mammary-digital-nail syndrome, 613689 (2), Autosomal dominant"				
chr22	31944492	31957602	22q12	22q12.3		113508	"YWHAH, YWHA1"	"Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide 22"	YWHAH	7533	ENSG00000128245			Ywhah (MGI:109194)			
chr22	32043031	32113028	22q13.1	22q12.3		182380	"SLC5A1, SGLT1"	"Solute carrier family 5 (sodium/glucose transporter), member 1"	SLC5A1	6523	ENSG00000100170		"Glucose/galactose malabsorption, 606824 (3), Autosomal recessive"	Slc5a1 (MGI:107678)			
chr22	32190434	32204848	22q12-q13	22q12.3		605969	RFPL2	RET finger protein-like 2	RFPL2	10739	ENSG00000128253						
chr22	32354884	32361160	22q12-q13	22q12.3		605970	RFPL3	RET finger protein-like 3	RFPL3	10738	ENSG00000128276						
chr22	32359905	32371263	22q12-q13	22q12.3		605971	RFPL3S	"Ret finger protein-like 3, antisense"	RFPL3S	10737							
chr22	32387574	32412286	22q12.3	22q12.3		613901	"RTCB, C22orf28, HSPC117"	"RNA 2-prime, 3-prime cyclic phosphate and 5-prime-OH ligase"	RTCB	51493	ENSG00000100220			Rtcb (MGI:106379)			
chr22	32413844	32464464	22q13	22q12.3		614109	"BPIFC, BPIL2"	"BPI fold-containing protein, family C"	BPIFC	254240	ENSG00000184459			Bpifc (MGI:3026884)			
chr22	32474681	32498830	22q12-q13	22q12.3		605648	"FBXO7, FBX7, FBX, PKPS, PARK15"	F-box only protein 7	FBXO7	25793	ENSG00000100225		"Parkinson disease 15, autosomal recessive, 260300 (3), Autosomal recessive"	Fbxo7 (MGI:1917004)			
chr22	32507819	33058390	22q12.3	22q12.3		602705	SYN3	Synapsin III	SYN3	8224	ENSG00000185666	?relation to schizophrenia		Syn3 (MGI:1351334)			
chr22	32800815	32863040	22q12.1-q13.2	22q12.3		188826	"TIMP3, SFD"	Tissue inhibitor of metalloproteinase-3	TIMP3	7078	ENSG00000100234		"Sorsby fundus dystrophy, 136900 (3), Autosomal dominant"	Timp3 (MGI:98754)			
chr22	33162236	33922840	22q12.3-q13.1	22q12.3		603590	"LARGE, KIAA0609, MDC1D, MDDGA6, MDDGB6"	Acetylglucosaminyltransferase-like protein	LARGE1	9215	ENSG00000133424		"Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, 613154 (3), Autosomal recessive; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6, 608840 (3), Autosomal recessive"	Large1 (MGI:1342270)			
chr22	35066135	35087386	22q12.3	22q12.3		612019	"ISX, RAXLX"	Intestine-specific homeobox	ISX	91464	ENSG00000175329			Isx (MGI:1918847)			
chr22	35256696	35295806	22q13.1	22q12.3		604702	"HMGXB4, HMG2L1"	HMG box domain-containing 4	HMGXB4	10042	ENSG00000100281			Hmgxb4 (MGI:1918073)			
chr22	35299274	35347993	22q13.1	22q12.3		604700	TOM1	"Target of MYB1, chicken, homolog of"	TOM1	10043	ENSG00000100284			Tom1 (MGI:1338026)			
chr22	35381066	35394213	22q12	22q12.3		141250	"HMOX1, HMOX1D"	Heme oxygenase 1	HMOX1	3162	ENSG00000100292		"Heme oxygenase-1 deficiency, 614034 (3); {Pulmonary disease, chronic obstructive, susceptibility to}, 606963 (3)"	Hmox1 (MGI:96163)			
chr22	35400122	35454941	22q13.1	22q12.3		602696	"MCM5, CDC46, MGORS8"	"Minichromosome maintenance, S. cerevisiae, homolog of, 5"	MCM5	4174	ENSG00000100297	mutation identified in 1 MGORS8 patient	"?Meier-Gorlin syndrome 8, 617564 (3), Autosomal recessive"	Mcm5 (MGI:103197)			
chr22	35540500	35554002	22q12.3	22q12.3		612842	"RASD2, RHES, TEM2"	"RASD family, member 2"	RASD2	23551	ENSG00000100302			Rasd2 (MGI:1922391)			
chr22	35606763	35623353	22q11.2-q13	22q12.3		160000	MB	Myoglobin	MB	4151	ENSG00000198125			Mb (MGI:96922)			
chr22	35648315	35668408	22q12.3	22q12.3		607256	APOL6	Apolipoprotein L6	APOL6	80830	ENSG00000221963			Apol6 (MGI:1919189)			
chr22	35708423	35730324	22q12.3	22q12.3		607255	APOL5	Apolipoprotein L5	APOL5	80831	ENSG00000128313						
chr22	35738733	36028891	22q13.1	22q12.3		612149	"RBFOX2, RBM9, FOX2, RTA"	"RNA binding protein, fox-1 homolog 2"	RBFOX2	23543	ENSG00000100320			Rbfox2 (MGI:1933973)			
chr22	36140322	36166176	22q12.3	22q12.3		607253	APOL3	Apolipoprotein L3	APOL3	80833	ENSG00000128284						
chr22	36189127	36204832	22q12.3	22q12.3		607254	APOL4	Apolipoprotein L4	APOL4	80832	ENSG00000100336		"{Schizophrenia}, 181500 (1), Autosomal dominant"				
chr22	36226208	36239953	22q12.3	22q12.3		607252	APOL2	Apolipoprotein L2	APOL2	23780	ENSG00000128335		"{Schizophrenia}, 181500 (1), Autosomal dominant"	Apol8 (MGI:2444921)			
chr22	36253070	36267530	22q12.3	22q12.3		603743	"APOL1, FSGS4"	Apolipoprotein L1	APOL1	8542	ENSG00000100342		"{End-stage renal disease, nondiabetic, susceptibility to}, 612551 (3); {Glomerulosclerosis, focal segmental, 4, susceptibility to}, 612551 (3)"				
chr22	36281276	36388066	22q11.2	22q12.3		160775	"MYH9, MHA, FTNS, DFNA17, BDPLT6"	"Myosin, heavy polypeptide-9, nonmuscle"	MYH9	4627	ENSG00000100345		"Deafness, autosomal dominant 17, 603622 (3), Autosomal dominant; Epstein syndrome, 153650 (3), Autosomal dominant; Fechtner syndrome, 153640 (3), Autosomal dominant; Macrothrombocytopenia and progressive sensorineural deafness, 600208 (3), Autosomal dominant; May-Hegglin anomaly, 155100 (3), Autosomal dominant; Sebastian syndrome, 605249 (3), Autosomal dominant"	Myh9 (MGI:107717)			
chr22	36467035	36482024	22q12.3	22q12.3		609063	"TXN2, TRX2, MTRX, COXPD29"	Thioredoxin 2	TXN2	25828	ENSG00000100348	mutation identified in 1 COXPD29 patient	"?Combined oxidative phosphorylation deficiency 29, 616811 (3), Autosomal recessive"	Txn2 (MGI:1929468)			
chr22	36487185	36507100	22q12.3	22q12.3		613777	"FOXRED2, ERFAD"	FAD-dependent oxidoreductase domain-containing protein 2	FOXRED2	80020	ENSG00000100350			Foxred2 (MGI:106315)			
chr22	36510849	36529229	22q13.1	22q12.3		603915	"EIF3D, EIF3S7"	"Eukaryotic translation initiation factor 3, subunit D"	EIF3D	8664	ENSG00000100353			Eif3d (MGI:1933181)			
chr22	36560868	36702857	22q13.1	22q12.3		602911	"CACNG2, MRD10"	"Calcium channel, voltage-dependent, gamma-2 subunit (stargazin)"	CACNG2	10369	ENSG00000166862	mutation identified one MRD10 patient	"?Mental retardation, autosomal dominant 10, 614256 (3)"	Cacng2 (MGI:1316660)			
chr22	36758201	36776132	22q12.3	22q12.3		615870	"IFT27, RABL4, BBS19"	"Intraflagellar transport 27, Chlamydomonas, homolog of"	IFT27	11020	ENSG00000100360	mutation identified in 1 BBS19 family	"?Bardet-Biedl syndrome 19, 615996 (3), Autosomal recessive"	Ift27 (MGI:1914292)			
chr22	36800700	36819472	22q12-q13.1	22q12.3		168890	PVALB	Parvalbumin	PVALB	5816	ENSG00000100362	?role in DiGeorge syndrome		Pvalb (MGI:97821)			
chr22	36860987	36878016	22q13.1	22q12.3		601488	"NCF4, P40PHOX, CGD3"	Neutrophil cytosolic factor-4	NCF4	4689	ENSG00000100365	mutation identified in 1 CGD3 patient	"?Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III, 613960 (3), Autosomal recessive"	Ncf4 (MGI:109186)			
chr22	36913573	36940448	22q12.2-q13.1	22q12.3		138981	"CSF2RB, SMDP5"	"Colony-stimulating factor-2 receptor, beta, low-affinity"	CSF2RB	1439	ENSG00000100368		"Surfactant metabolism dysfunction, pulmonary, 5, 614370 (3), Autosomal recessive"	"Csf2rb2,Csf2rb (MGI:1339759,MGI:1339760)"			
chr22	37010858	37020182	22q11.2-qter	22q12.3		180370	"TST, RDS"	Thiosulfate sulfurtransferase (Rhodanese)	TST	7263	ENSG00000128311			Tst (MGI:98852)			
chr22	37019641	37029821	22q11.2-qter	22q12.3		602496	MPST	Mercaptopyruvate sulfurtransferase	MPST	4357	ENSG00000128309			Mpst (MGI:2179733)			
chr22	37051724	37063389	22q12.3	22q12.3		616386	KCTD17	Potassium channel tetramerization domain-containing protein 17	KCTD17	79734	ENSG00000100379		"Dystonia 26, myoclonic, 616398 (3), Autosomal dominant"	Kctd17 (MGI:1920094)			
chr22	37065435	37110624	22q12-q13	22q12.3		609862	"TMPRSS6, IRIDA"	"Transmembrane protease, serine 6 (matriptase 2)"	TMPRSS6	164656	ENSG00000187045		"Iron-refractory iron deficiency anemia, 206200 (3), Autosomal recessive"	Tmprss6 (MGI:1919003)			
chr22	37125837	37175117	22q11.2-q13	22q12.3		146710	IL2RB	"Interleukin-2 receptor, beta polypeptide"	IL2RB	3560	ENSG00000100385			Il2rb (MGI:96550)			
chr22	37180165	37199400	22q12.3	22q12.3		614910	"C1QTNF6, CTFP6"	C1q- and tumor necrosis factor-related protein 6	C1QTNF6	114904	ENSG00000133466			C1qtnf6 (MGI:1919959)			
chr22	37200000	50818468	22q13			615538	"DUP22q13, C22DUPq13"	Chromosome 22q13 duplication syndrome					"Chromosome 22q13 duplication syndrome, 615538 (4), Isolated cases"				
chr22	37200000	50818468	22q13			610873	MENAQ1	"Menarche, age at, QTL 1"		100188822		max lod at UT7136	"{Menarche, age at, QTL}, 610873 (2)"				
chr22	37200000	50818468	22q13			613282	NAFLD1	"Fatty liver disease, nonalcoholic, susceptibility to, 1"		100380876		associated with rs738409	"{Fatty liver disease, nonalcoholic, susceptibility to, 1}, 613282 (2), Multifactorial"				
chr22	37200000	50818468	22q13			612417	NRCLP4	Narcolepsy 4		100216484		associated with rs5770917	"{Narcolepsy 4}, 612417 (2)"				
chr22	37204236	37220450	22q13.1	22q13.1		182453	SSTR3	Somatostatin receptor-3	SSTR3	6753	ENSG00000278195			Sstr3 (MGI:98329)			
chr22	37225260	37244298	22q12.3-q13.2	22q13.1		602049	RAC2	"Ras-related C3 botulinum toxin substrate 3 (rho family, small GTP-binding protein Rac2)"	RAC2	5880	ENSG00000128340		"Neutrophil immunodeficiency syndrome, 608203 (3)"	Rac2 (MGI:97846)			
chr22	37282382	37315347	22q12.3-q13.1	22q13.1		606514	"CYTH4, PSCD4, CYT4"	Cytohesin 4	CYTH4	27128	ENSG00000100055			Cyth4 (MGI:2441702)			
chr22	37469062	37486439	22q12	22q13.1		602577	MFNG	Manic fringe	MFNG	4242	ENSG00000100060			Mfng (MGI:1095404)			
chr22	37490361	37519202	22q13.1	22q13.1		607209	"CARD10, CARMA3, BIMP1"	Caspase recruitment domain-containing protein 10	CARD10	29775	ENSG00000100065			Card10 (MGI:2146012)			
chr22	37559777	37569404	22q13.1	22q13.1		606084	"CDC42EP1, MSE55, BORG5, CEP1"	CDC42 effector protein 1	CDC42EP1	11135	ENSG00000128283			Cdc42ep1 (MGI:1929763)			
chr22	37570245	37580016	22q13.1	22q13.1		150571	LGALS2	"Lectin, galactoside-binding, soluble, 2"	LGALS2	3957	ENSG00000100079		"{Myocardial infarction, susceptibility to}, 608446 (3)"	Lgals2 (MGI:895068)			
chr22	37608473	37633563	22q13.31	22q13.1		606004	GGA1	"Golgi associated, gamma adaptin ear containing, ARF binding protein 1"	GGA1	26088	ENSG00000100083			Gga1 (MGI:2146207)			
chr22	37639474	37656118	22q13.1	22q13.1		617368	"SH3BP1, ARHGAP43, BGIN"	SH3 domain-binding protein 1	SH3BP1	23616	ENSG00000100092			Sh3bp1 (MGI:104603)			
chr22	37675605	37679801	22q12-q13.1	22q13.1		150570	LGALS1	"Lectin, galactose-binding, soluble, 1"	LGALS1	3956	ENSG00000100097			Lgals1 (MGI:96777)			
chr22	37696987	37776555	22q13.1	22q13.1		609761	"TRIOBP, KIAA1662"	Trio- and F-actin-binding protein	TRIOBP	11078	ENSG00000100106		"Deafness, autosomal recessive 28, 609823 (3), Autosomal recessive"	Triobp (MGI:1349410)			
chr22	37805106	37807435	22q13.1	22q13.1		142708	"H1F0, H1FV"	"H1 histone family, member 0"	H1F0	3005	ENSG00000189060			H1f0 (MGI:95893)			
chr22	37807893	37817176	22q12-q13	22q13.1		607422	"GCAT, KBL"	Glycine C-acetyltransferase	GCAT	23464	ENSG00000100116			Gcat (MGI:1349389)			
chr22	37823381	37825494	22q12.2-q13.1	22q13.1		603692	GALR3	Galanin receptor 3	GALR3	8484	ENSG00000128310			Galr3 (MGI:1329003)			
chr22	37830852	37849317	22q13.1	22q13.1		613383	"ANKRD54, LIAR"	Ankyrin repeat domain-containing protein 54	ANKRD54	129138	ENSG00000100124			Ankrd54 (MGI:2444209)			
chr22	37847677	37847773	22q13.1	22q13.1		613556	MIR659	Micro RNA 659	MIR659	724029							
chr22	37953662	38041914	22q13.1	22q13.1		604414	POLR2F	"Polymerase II, RNA, subunit F"	POLR2F	5435	ENSG00000100142			Polr2f (MGI:1349393)			
chr22	37972311	37984531	22q13	22q13.1		602229	"SOX10, WS4, WS4C, PCWH"	SRY (sex-determining region Y)-box-10	SOX10	6663	ENSG00000100146	megacolon and spotting in mice	"PCWH syndrome, 609136 (3), Autosomal dominant; Waardenburg syndrome, type 2E, with or without neurologic involvement, 611584 (3), Autosomal dominant; Waardenburg syndrome, type 4C, 613266 (3), Autosomal dominant"	Sox10 (MGI:98358)			
chr22	38056310	38075703	22q12.3-q13.2	22q13.1		605926	"PICK1, PRKCABP"	Protein interacting with C kinase 1	PICK1	9463	ENSG00000100151			Pick1 (MGI:894645)			
chr22	38078136	38083162	22q12.3-q13.2	22q13.1		610409	"SLC16A8, MCT3"	"Solute carrier family 16 (monocarboxylic acid transporter), member 8"	SLC16A8	23539	ENSG00000100156			Slc16a8 (MGI:1929519)			
chr22	38084888	38110943	22q13.1	22q13.1		617536	"BAIAP2L2, PINKBAR"	Bai1-associated protein 2-like 2	BAIAP2L2	80115	ENSG00000128298			Baiap2l2 (MGI:2652819)			
chr22	38111494	38192099	22q13.1	22q13.1		603604	"PLA2G6, IPLA2, INAD1, NBIA2B, NBIA2A, PARK14"	"Phospholipase A2, group VI"	PLA2G6	8398	ENSG00000184381		"Infantile neuroaxonal dystrophy 1, 256600 (3), Autosomal recessive; Neurodegeneration with brain iron accumulation 2B, 610217 (3), Autosomal recessive; Parkinson disease 14, autosomal recessive, 612953 (3), Autosomal recessive"	Pla2g6 (MGI:1859152)			
chr22	38201931	38216510	22q12.2-q13.2	22q13.1		604877	MAFF	"v-MAF avian musculoaponeurotic fibrosarcoma oncogene family, protein F"	MAFF	23764	ENSG00000185022			Maff (MGI:96910)			
chr22	38290690	38318083	22q12-q13	22q13.1		600863	CSNK1E	"Casein kinase-1, epsilon"	CSNK1E	1454	ENSG00000213923			Csnk1e (MGI:1351660)			
chr22	38426326	38455198	22q13.1	22q13.1		600504	"KCNJ4, HIR"	"Potassium inwardly-rectifying channel, subfamily J, member 4"	KCNJ4	3761	ENSG00000168135			Kcnj4 (MGI:104743)			
chr22	38483437	38506339	22q13.1	22q13.1		608469	"DDX17, RH70, P72"	DEAD/H box-17	DDX17	10521	ENSG00000100201			Ddx17 (MGI:1914290)			
chr22	38509153	38570285	22q13.1	22q13.1		602721	"DMC1, LIM15"	"Disrupted meiotic cDNA 1, yeast, homolog of"	DMC1	11144	ENSG00000100206			Dmc1 (MGI:105393)			
chr22	38656652	38673849	22q12-q13	22q13.1		607757	"CBY, C22orf2, HS508I15A"	Chibby	CBY1	25776	ENSG00000100211			Cby1 (MGI:1920989)			
chr22	38681948	38684759	22q12-q13	22q13.1		607046	"TOMM22, TOM22"	"Translocase of outer mitochondrial membrane 22, yeast, homolog of"	TOMM22	56993	ENSG00000100216			Tomm22 (MGI:2450248)			
chr22	38683915	38701417	22q13.1	22q13.1		615323	"JOSD1, KIAA0063"	Josephin domain-containing protein 1	JOSD1	9929	ENSG00000100221						
chr22	38704560	38738264	22q12-q13.1	22q13.1		602245	"GTPBP1, GP1"	GTP-binding protein 1	GTPBP1	9567	ENSG00000100226			Gtpbp1 (MGI:109443)			
chr22	38734713	38756018	22q12-q13	22q13.1		613569	"SUN2, UNC84B, KIAA0668"	SAD1 and UNC84 domain-containing protein 2	SUN2	25777	ENSG00000100242			Sun2 (MGI:2443011)			
chr22	38778507	38794155	22q13.1	22q13.1		610565	"DNAL4, MRMV3"	"Dynein, axonemal, light chain 4"	DNAL4	10126	ENSG00000100246	mutation identified in 1 MRMV3 family	"?Mirror movements 3, 616059 (3), Autosomal recessive"	Dnal4 (MGI:1859217)			
chr22	38861426	38872333	22q13.1	22q13.1		617438	CBX6	Chromobox homolog 6	CBX6	23466	ENSG00000183741			Cbx6 (MGI:3512628)			
chr22	38957521	38963182	22q13	22q13.1		607109	"APOBEC3A, PHRBN"	"Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A (phorbolin 1)"	APOBEC3A	200315	ENSG00000128383						
chr22	38982398	38992778	22q13	22q13.1		607110	"APOBEC3B, PHRBNL"	"Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B"	APOBEC3B	9582	ENSG00000179750			Apobec3 (MGI:1933111)			
chr22	39014235	39020351	22q13	22q13.1		607750	APOBEC3C	"Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3C"	APOBEC3C	27350	ENSG00000244509						
chr22	39019080	39055971	22q12-q13.2	22q13.1		608993	APOBEC3F	"Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3F"	APOBEC3F	200316	ENSG00000128394						
chr22	39077004	39087742	22q12-q13.2	22q13.1		607113	"APOBEC3G, MDS019, CEM15, FLJ12740"	"Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G"	APOBEC3G	60489	ENSG00000239713						
chr22	39097202	39104066	22q13.1	22q13.1		610976	"APOBEC3H, ARP10"	"Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3H"	APOBEC3H	164668	ENSG00000100298						
chr22	39130771	39152649	22q13.1	22q13.1		608457	CBX7	Chromobox homolog 7	CBX7	23492	ENSG00000100307			Cbx7 (MGI:1196439)			
chr22	39223358	39245054	22q12.3-q13.1	22q13.1		190040	"PDGFB, SIS, IBGC5"	"Platelet-derived growth factor, beta polypeptide (oncogene SIS)"	PDGFB	5155	ENSG00000100311	fused with COL1A1 in DFSP	"Basal ganglia calcification, idiopathic, 5, 615483 (3), Autosomal dominant; Dermatofibrosarcoma protuberans, 607907 (3); Meningioma, SIS-related, 607174 (3), Autosomal dominant"	Pdgfb (MGI:97528)			
chr22	39312881	39319664	22q	22q13.1		604163	RPL3	Ribosomal protein L3	RPL3	6122	ENSG00000100316			Rpl3 (MGI:1351605)			
chr22	39313818	39313910	22q13	22q13.1		611071	"SNORD83B, RNU83B"	"Small nucleolar RNA, C/D box, 83B"	SNORD83B	116938							
chr22	39315212	39315306	22q13	22q13.1		611070	"SNORD83A, RNU83A"	"Small nucleolar RNA, C/D box, 83A"	SNORD83A	116937							
chr22	39316841	39316895	22q13	22q13.1		611069	RNU86	"RNA, U86 small nucleolar"	SNORD139	116936							
chr22	39319051	39319112	22q13	22q13.1		611068	"SNORD43, RNU43"	"Small nucleolar RNA, C/D box, 43"	SNORD43	26807							
chr22	39349948	39385587	22q13	22q13.1		603925	SYNGR1	Synaptogyrin 1	SYNGR1	9145	ENSG00000100321			Syngr1 (MGI:1328323)			
chr22	39399753	39437126	22q13.1	22q13.1		602615	"TAB1, MAP3K7IP1"	Tak1 (MAP3K7) binding protein 1	TAB1	10454	ENSG00000100324			Tab1 (MGI:1913763)			
chr22	39447166	39492193	22q13.1	22q13.1		604621	"MGAT3, GNT3"	"Beta-1,4-mannosyl-glycoprotein beta-1,4-N-acetylglucosaminyltransferase"	MGAT3	4248	ENSG00000128268			Mgat3 (MGI:104532)			
chr22	39500099	39518133	22q13.1	22q13.1		615497	"MEIF1, SMCR7L, MID51"	Mitochondrial elongation factor 1	MIEF1	54471	ENSG00000100335			Mief1 (MGI:2146020)			
chr22	39514493	39522685	22q13.1	22q13.1		604064	"ATF4, CREB2, TAXREB67"	Activating transcription factor 4	ATF4	468	ENSG00000128272			Atf4 (MGI:88096)			
chr22	39529092	39532854	22q13.1	22q13.1		610225	"RPS19BP1, S19BP, MGC52010"	Ribosomal protein S19 binding protein 1	RPS19BP1	91582	ENSG00000187051			Rps19bp1 (MGI:1913788)			
chr22	39570752	39689736	22q13.1	22q13.1		608230	"CACNA1I, KIAA1120"	"Calcium channel, voltage-dependent, T type, alpha-1I subunit"	CACNA1I	8911	ENSG00000100346			Cacna1i (MGI:2178051)			
chr22	39901072	39973342	22q12-qter	22q13.1		604518	"GRAP2, GRID"	GRB2-related adaptor protein 2	GRAP2	9402	ENSG00000100351			Grap2 (MGI:1333842)			
chr22	40044816	40335807	22q13.1	22q13.1		610740	"TNRC6B, KIAA1093"	Trinucleotide repeat-containing gene 6B	TNRC6B	23112	ENSG00000100354			Tnrc6b (MGI:2443730)			
chr22	40346499	40387407	22q13.1	22q13.1		608222	ADSL	Adenylosuccinate lyase	ADSL	158	ENSG00000239900	ade(-)I; bifunctional	"Adenylosuccinase deficiency, 103050 (3), Autosomal recessive"	Adsl (MGI:103202)			
chr22	40370561	40410288	22q13.1	22q13.1		610440	"SGSM3, RUTBC3, MAP, RUSC3"	Small G protein signaling modulator 3	SGSM3	27352	ENSG00000100359			Sgsm3 (MGI:1916329)			
chr22	40410280	40636861	22q13	22q13.1-q13.2		606078	"MKL1, AMKL, MAL"	Megakaryoblastic leukemia 1 gene	MKL1	57591	ENSG00000196588	fusion with RBM15	"Megakaryoblastic leukemia, acute (3)"	Mkl1 (MGI:2384495)			
chr22	40679177	40682813	22q13.3	22q13.2		601751	"MCHR1, GPR24, SLC1"	Melanin-concentrating hormone receptor 1	MCHR1	2847	ENSG00000128285			Mchr1 (MGI:2180756)			
chr22	40769629	40819398	22q13	22q13.2		606795	"SLC25A17, PMP34"	"Solute carrier family 25 (mitochondrial carrier), member 17 (peroxisomal membrane protein, 34kD)"	SLC25A17	10478	ENSG00000100372			Slc25a17 (MGI:1342248)			
chr22	40824534	40857007	22q13	22q13.2		606796	"ST13, P48, HOP"	Suppression of tumorigenicity 13	ST13	6767	ENSG00000100380			St13 (MGI:1917606)			
chr22	40857080	40932818	22q13.31-q13.33	22q13.2		613553	"XPNPEP3, APP3, NPHPL1"	X-prolyl aminopeptidase 3	XPNPEP3	63929	ENSG00000196236		"Nephronophthisis-like nephropathy 1, 613159 (3), Autosomal recessive"				
chr22	40859548	40862125	22q13.2	22q13.2		611336	"DNAJB7, DJ5, HSC3"	"DNAJ/HSP40 homolog, subfamily B, member 7"	DNAJB7	150353	ENSG00000172404			Dnajb7 (MGI:1914012)			
chr22	40951346	40973014	22q13.2	22q13.2		603814	"RBX1, ROC1"	RING-box 1	RBX1	9978	ENSG00000100387			Rbx1-ps (MGI:3710517)			
chr22	41092585	41180076	22q13	22q13.2		602700	"EP300, RSTS2"	"E1A-binding protein, 300kD"	EP300	2033	ENSG00000100393		"Colorectal cancer, somatic, 114500 (3); Rubinstein-Taybi syndrome 2, 613684 (3), Autosomal dominant"	Ep300 (MGI:1276116)			
chr22	41205191	41231270	22q13.3	22q13.2		611865	"L3MBTL2, L3MBT"	L3MBT-like 2	L3MBTL2	83746	ENSG00000100395			L3mbtl2 (MGI:2443584)			
chr22	41229509	41241770	22q13.2	22q13.2		616236	CHADL	Chondroadherin-like	CHADL	150356	ENSG00000100399			Chadl (MGI:3036284)			
chr22	41244776	41302212	22q13.2	22q13.2		602362	RANGAP1	"GTPase-activating protein, RAN, 1"	RANGAP1	5905	ENSG00000100401			Rangap1 (MGI:103071)			
chr22	41367332	41399327	22q13	22q13.2		188595	TEF	Thyrotroph embryonic factor	TEF	7008	ENSG00000167074			Tef (MGI:98663)			
chr22	41433487	41448229	22q13.1-q13.31	22q13.2		607396	"TOB2, KIAA1663"	"Transducer of erbb2, 2"	TOB2	10766	ENSG00000183864			Tob2 (MGI:1888525)			
chr22	41459716	41468703	22q13.2	22q13.2		617846	"PHF5A, SF3B7, SF3B14B"	PHD finger protein 5A	PHF5A	84844	ENSG00000100410			Phf5a (MGI:2156864)			
chr22	41468755	41528988	22q13.2	22q13.2		100850	"ACO2, ICRD, OPA9"	"Aconitase, mitochondrial"	ACO2	50	ENSG00000100412	distal to Ph1 break; mutation identified in 1 OPA9 family	"Infantile cerebellar-retinal degeneration, 614559 (3), Autosomal recessive; ?Optic atrophy 9, 616289 (3), Autosomal recessive"	Aco2 (MGI:87880)			
chr22	41561009	41576665	22q13.2	22q13.2		617689	"CSDC2, PIPPIN"	Cold-shock domain-containing protein C2	CSDC2	27254	ENSG00000172346			Csdc2 (MGI:2146027)			
chr22	41576885	41589866	22q13.1	22q13.2		601786	PMM1	Phosphomannomutase 1	PMM1	5372	ENSG00000100417			Pmm1 (MGI:1353418)			
chr22	41598027	41621076	22q13.2	22q13.2		614637	"DESI1, PPPDE2"	Desumoylating isopeptidase 1	DESI1	27351	ENSG00000100418			Desi1 (MGI:106313)			
chr22	41621162	41664047	22q11-q13	22q13.2		152690	"XRCC6, G22P1, TLAA, Ku70"	"X-ray repair, complementing defecting, in chinese hamster, 6"	XRCC6	2547	ENSG00000196419	tight linkage to CYP2D		Xrcc6 (MGI:95606)			
chr22	41673932	41690491	22q13.2	22q13.2		601304	NHP2L1	"Non-histone chromosome protein 2, S. cerevisiae, like 1"	SNU13	4809	ENSG00000100138	previously assigned to 12q24.3 by FISH		Snu13 (MGI:893586)			
chr22	41833078	41907307	22q13	22q13.2		600481	SREBF2	Sterol regulatory element binding transcription factor 2	SREBF2	6721	ENSG00000198911			Srebf2 (MGI:107585)			
chr22	41900943	41901011	22q13.2	22q13.2		612156	"MIR33A, MIRN33A"	Micro RNA 33A	MIR33A	407039							
chr22	41906048	41915094	22q13.2	22q13.2		617329	SHISA8	"Shisa family, member 8"	SHISA8	440829	ENSG00000234965			Shisa8 (MGI:2146080)			
chr22	41925031	41926816	22q13.1-q13.31	22q13.2		606269	"TNFRSF13C, BAFFR, CVID4"	"Tumor necrosis factor receptor superfamily, member 13C"	TNFRSF13C	115650	ENSG00000159958		"Immunodeficiency, common variable, 4, 613494 (3), Autosomal recessive"	Tnfrsf13c (MGI:1919299)			
chr22	41927746	41947163	22q13.31	22q13.2		610152	"PANE1, C22orf18"	Proliferation-associated nuclear element 1	CENPM	79019	ENSG00000100162			Cenpm (MGI:1913820)			
chr22	41969454	41998220	22q13.2	22q13.2		608314	"SEPT3, SEP3"	Septin 3	3-Sep	55964	ENSG00000100167			Sept3 (MGI:1345148)			
chr22	41995102	42059401	22q13.2	22q13.2		610981	"WBP2NL, PAWP"	WWBP2 N-terminal-like protein	WBP2NL	164684	ENSG00000183066			Wbp2nl (MGI:1921966)			
chr22	42058333	42070895	22q11	22q13.2		104170	NAGA	"Acetylgalactosaminidase, alpha-N- (alpha-galactosidase B)"	NAGA	4668	ENSG00000198951	proximal to Ph1 break	"Kanzaki disease, 609242 (3), Autosomal recessive; Schindler disease, type I, 609241 (3), Autosomal recessive; Schindler disease, type III, 609241 (3), Autosomal recessive"	Naga (MGI:1261422)			
chr22	42074243	42079437	22q13.2	22q13.2		614240	"FAM109B, SES2, IPIP27B"	"Family with sequence similarity 109, member B"	PHETA2	150368	ENSG00000177096			Fam109b (MGI:2443609)			
chr22	42079690	42084283	22q13.2	22q13.2		615588	"SMDT1, EMRE, C22orf32"	Single-pass membrane protein with aspartate-rich tail 1	SMDT1	91689	ENSG00000183172			Smdt1 (MGI:1916279)			
chr22	42085525	42090954	22q13.1	22q13.2		602138	NDUFA6	"NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6"	NDUFA6	4700	ENSG00000184983	previously assigned to 21q22		Ndufa6 (MGI:1914380)			
chr22	42126498	42130880	22q13.1	22q13.2		124030	"CYP2D6, CPD6, P450DB1"	"Cytochrome P450, subfamily IID, polypeptide 6"	CYP2D6	1565	ENSG00000100197		"{Codeine sensitivity}, 608902 (3), Autosomal recessive; {Debrisoquine sensitivity}, 608902 (3), Autosomal recessive"				
chr22	42160012	42283926	22q13.3	22q13.2		603107	"TCF20, SPBP, AR1"	Transcription factor 20	TCF20	6942	ENSG00000100207			Tcf20 (MGI:108399)			
chr22	42380406	42438154	22q13.2	22q13.2		608740	"NFAM1, CNAIP"	NFAT activating protein with ITAM motif 1	NFAM1	150372	ENSG00000235568			Nfam1 (MGI:1921289)			
chr22	42500578	42512559	22q13.2	22q13.2		607979	SERHL	Serine hydrolase-like	SERHL	94009							
chr22	42583720	42614961	22q13.2	22q13.2		611520	"POLDIP3, SKAR, PDIP46"	Polymerase delta-interacting protein 3	POLDIP3	84271	ENSG00000100227			Poldip3 (MGI:1921076)			
chr22	42617839	42649398	22q13.31-qter	22q13.2		613213	"CYB5R3, DIA1, B5R"	Cytochrome b5 reductase 3	CYB5R3	1727	ENSG00000100243		"Methemoglobinemia, type I, 250800 (3), Autosomal recessive; Methemoglobinemia, type II, 250800 (3), Autosomal recessive"				
chr22	42692111	42721300	22q13.2	22q13.2		607922	"A4GALT, P1PK"	"Alpha 1,4-galactosyltransferase"	A4GALT	53947	ENSG00000128274		"[Blood group, P1Pk system, P(2) phenotype], 111400 (3); [Blood group, P1Pk system, p phenotype], 111400 (3); NOR polyagglutination syndrome, 111400 (3)"	A4galt (MGI:3512453)			
chr22	42796525	42857401	22q13.2	22q13.2		612439	ARFGAP3	ADP-ribosylation factor GTPase-activating protein 3	ARFGAP3	26286	ENSG00000242247			Arfgap3 (MGI:1913501)			
chr22	42869765	43016173	22q13.2	22q13.2		604960	PACSIN2	Protein kinase C and casein kinase substrate in neurons 2	PACSIN2	11252	ENSG00000100266			Pacsin2 (MGI:1345153)			
chr22	43039515	43089427	22q13.1	22q13.2		608955	"TTLL1, KIAA0173"	tubulin tyrosine ligase-like protein 1	TTLL1	25809	ENSG00000100271			Ttll1 (MGI:2443047)			
chr22	43110747	43129711	22q13.3	22q13.2		603392	"BIK, NBK"	Bcl2-interacting killer	BIK	638	ENSG00000100290			Bik (MGI:1206591)			
chr22	43132205	43143396	22q13.31	22q13.2		614479	MCAT	"Malonyl CoA:ACP acyltransferase, mitochondrial"	MCAT	27349	ENSG00000100294			Mcat (MGI:2388651)			
chr22	43151513	43163241	22q13.31	22q13.2		109610	"TSPO, BZRP, PBR, PBS, BPBS"	"Translocator protein, 18kD (benzodiazepine receptor, peripheral type)"	TSPO	706	ENSG00000100300			Tspo (MGI:88222)			
chr22	43203222	43343387	22q13	22q13.2		611746	SCUBE1	"Signal peptide-, CUB domain-, and EGF-like domains-containing protein 1"	SCUBE1	80274	ENSG00000159307			Scube1 (MGI:1890616)			
chr22	43412013	43507847	22q13.31	22q13.2		602112	"MPPED1, C22orf1, 239AB"	Metallophosphoesterase domain-containing protein 1	MPPED1	758	ENSG00000186732			Mpped1 (MGI:106316)			
chr22	43824506	43862497	22q13.31	22q13.31		608359	"SULT4A1, BRSTL1"	"Sulfotransferase family 4A, member 1"	SULT4A1	25830	ENSG00000130540			Sult4a1 (MGI:1888971)			
chr22	43879677	43892012	22q13.31	22q13.31		611589	"PNPLA5, GS2L"	Patatin-like phospholipase domain-containing 5	PNPLA5	150379	ENSG00000100341			Pnpla5 (MGI:1923022)			
chr22	43923738	43947567	22q13	22q13.31		609567	"PNPLA3, ADPN"	Patatin-like phospholipase domain-containing protein 3	PNPLA3	80339	ENSG00000100344			Pnpla3 (MGI:2151796)			
chr22	43955380	43996531	22q13.31	22q13.31		612058	"SAMM50, SAM50"	"Sorting and assembly machinery component 50, S. cerevisiae, homolog of"	SAMM50	25813	ENSG00000100347			Samm50 (MGI:1915903)			
chr22	43999163	44169232	22q13.31	22q13.31		608121	PARVB	"Parvin, beta"	PARVB	29780	ENSG00000188677			Parvb (MGI:2153063)			
chr22	44170227	44208468	22q13.31	22q13.31		608122	PARVG	"Parvin, gamma"	PARVG	64098	ENSG00000138964			Parvg (MGI:2158329)			
chr22	44668546	44737680	22q13.31	22q13.31		609406	"PRR5, PP610"	Proline-rich protein 5	PRR5	55615	ENSG00000186654			Prr5 (MGI:1924714)			
chr22	44752557	44862783	22q13.31	22q13.31		609405	"ARHGAP8, BPGAP1"	"GTPase-activating protein, RHO, 8"	ARHGAP8	23779	ENSG00000241484			Arhgap8 (MGI:1920417)			
chr22	44881161	45009927	22q13.31	22q13.31		616727	"PHF21B, PHF4, BHC80L"	PHD finger protein 21B	PHF21B	112885	ENSG00000056487			Phf21b (MGI:2443812)			
chr22	45163844	45188010	22q13.3	22q13.31		604646	"NUP50, NPAP60L, NPAP60"	"Nucleoporin, 50 kD"	NUP50	10762	ENSG00000093000			Nup50 (MGI:1351502)			
chr22	45284986	45295873	22q13.31	22q13.31		611559	"UPK3A, UPK3, UPIII"	Uroplakin 3A	UPK3A	7380	ENSG00000100373			Upk3a (MGI:98914)			
chr22	45502838	45601133	22q13.3	22q13.31		135820	FBLN1	Fibulin 1	FBLN1	2192	ENSG00000077942		"Synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostoses, 608180 (4), Autosomal dominant"	Fbln1 (MGI:95487)			
chr22	45671797	45845306	22q13	22q13.31		611150	"ATXN10, SCA10"	Ataxin 10	ATXN10	25814	ENSG00000130638	ATTCTn repeat in intron 9	"Spinocerebellar ataxia 10, 603516 (3), Autosomal dominant"	Atxn10 (MGI:1859293)			
chr22	45920361	45977127	22q13	22q13.31		601967	WNT7B	"Wingless-type MMTV integration site family, member-7B"	WNT7B	7477	ENSG00000188064			Wnt7b (MGI:98962)			
chr22	46112748	46112821	22q13.31	22q13.31		612143	"MIRLET7A3, LET7A3, MIRNLET7A3"	Micro RNA let7a3	MIRLET7A3	406883							
chr22	46113685	46113767	22q13	22q13.31		611249	"MIRLET7B, LET7B, MIRNLET7B"	Micro RNA Let7B	MIRLET7B	406884							
chr22	46150533	46243755	22q12-q13.1	22q13.31		170998	"PPARA, PPAR"	Peroxisome proliferator-activated receptor-alpha	PPARA	5465	ENSG00000186951		"{Hyperapobetalipoproteinemia, susceptibility to} (3)"	Ppara (MGI:104740)			
chr22	46255662	46263321	22q13.3	22q13.31		604670	PKDREJ	Polycystic kidney disease and sea urchin REJ homolog-like	PKDREJ	10343	ENSG00000130943			Pkdrej (MGI:1338786)			
chr22	46335400	46357339	22q13	22q13.31		610230	"TRMU, MTO2"	tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase	TRMU	55687	ENSG00000100416		"{Deafness, mitochondrial, modifier of}, 580000 (3), Mitochondrial; Liver failure, transient infantile, 613070 (3), Autosomal recessive"	Trmu (MGI:1919276)			
chr22	46360833	46537501	22q13.3	22q13.31		604523	CELSR1	Cadherin EGF LAG seven-pass G-type receptor 1	CELSR1	9620	ENSG00000075275			Celsr1 (MGI:1100883)			
chr22	46576016	46682754	22q13.31	22q13.31		613691	"GRAMD4, KIAA0767, DIP"	Gram domain-containing protein 4	GRAMD4	23151	ENSG00000075240			Gramd4 (MGI:2676308)			
chr22	46684409	46738254	22q13	22q13.31		610307	"CERK, KIAA1646"	Ceramide kinase	CERK	64781	ENSG00000100422			Cerk (MGI:2386052)			
chr22	46762616	47224974	22q13.31	22q13.31		616879	"TBC1D22A, C22orf4"	"TBC1 domain family, member 22A"	TBC1D22A	25771	ENSG00000054611			Tbc1d22a (MGI:1289265)			
chr22	48489459	48751934	22q13.32	22q13.32		617499	"FAM19A5, TAFA5"	"Family with sequence similarity 19, member A5, CC motif chemokine-like"	FAM19A5	25817	ENSG00000219438			Fam19a5 (MGI:2146182)			
chr22	49773277	49827926	22q13	22q13.33		604589	BRL	BR140-like gene	BRD1	23774	ENSG00000100425			Brd1 (MGI:1924161)			
chr22	49853848	49890077	22q13.33	22q13.33		612552	"ZBED4, KIAA0637"	Zinc finger BED domain-containing protein 4	ZBED4	9889	ENSG00000100426						
chr22	49860162	49918468	22q13.33	22q13.33		607144	"ALG12, CDG1G"	Dolichyl-P-mannose:Man-7-GlcNAc-2-PP-dolichyl-alpha-6- mannosyltransferase	ALG12	79087	ENSG00000182858		"Congenital disorder of glycosylation, type Ig, 607143 (3)"	Alg12 (MGI:2385025)			
chr22	49960494	49964071	22q13.33	22q13.33		610580	PIM3	Oncogene PIM3	PIM3	415116	ENSG00000198355			Pim3 (MGI:1355297)			
chr22	49993577	50013826	22q13	22q13.33		613414	IL17REL	Interleukin 17 receptor E-like	IL17REL	400935	ENSG00000188263						
chr22	50059390	50085928	22q13.33	22q13.33		605908	"MLC1, LVM, VL"	MLC1 gene	MLC1	23209	ENSG00000100427		"Megalencephalic leukoencephalopathy with subcortical cysts, 604004 (3), Autosomal recessive"	Mlc1 (MGI:2157910)			
chr22	50090005	50161704	22q13.33	22q13.33		605794	MOV10L1	Mov10-like 1	MOV10L1	54456	ENSG00000073146			Mov10l1 (MGI:1891384)			
chr22	50170730	50180294	22q13	22q13.33		608421	"PANX2, PX2"	Pannexin 2	PANX2	56666	ENSG00000073150			Panx2 (MGI:1890615)			
chr22	50200978	50217615	22q13.33	22q13.33		607917	"SELENOO, SELO"	Selenoprotein O	SELENOO	83642	ENSG00000073169			Selenoo (MGI:1919007)			
chr22	50217688	50245027	22q13.33	22q13.33		610053	"TUBGCP6, GCP6, KIAA1669, MCCRP1"	Tubulin-gamma complex-associated protein 6	TUBGCP6	85378	ENSG00000128159		"Microcephaly and chorioretinopathy, autosomal recessive, 1, 251270 (3), Autosomal recessive"	Tubgcp6 (MGI:2146071)			
chr22	50252900	50261809	22q13.3	22q13.33		602399	"MAPK12, SAPK3, ERK3"	Mitogen-activated protein kinase 12 (Stress-activated protein kinase-3)	MAPK12	6300	ENSG00000188130			Mapk12 (MGI:1353438)			
chr22	50274978	50307636	22q13.31-q13.33	22q13.33		604293	"PLXNB2, MM1"	Plexin B2	PLXNB2	23654	ENSG00000196576			Plxnb2 (MGI:2154239)			
chr22	50343316	50445089	22q13.33	22q13.33		610877	"SAPS2, PP6R2, KIAA0685"	"SAPS domain family, member 2"	PPP6R2	9701	ENSG00000100239			Ppp6r2 (MGI:1918724)			
chr22	50444999	50475070	22q13.33	22q13.33		603560	"SBF1, MTMR5, CMT4B3"	SET-binding factor 1 (myotubularin-related protein 5)	SBF1	6305	ENSG00000100241		"Charcot-Marie-Tooth disease, type 4B3, 615284 (3), Autosomal recessive"	Sbf1 (MGI:1925230)			
chr22	50508215	50524779	22q13.33	22q13.33		611230	"NCAPH2, CAPH2"	Non-SMC condensin II complex subunit H2	NCAPH2	29781	ENSG00000025770			Ncaph2 (MGI:1289164)			
chr22	50523567	50526438	22q13	22q13.33		604272	"SCO2, CEMCOX1, MYP6"	SCO2 cytochrome c oxidase assembly protein	SCO2	9997	ENSG00000130489		"Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3), Autosomal recessive; Myopia 6, 608908 (3), Autosomal dominant"	Sco2 (MGI:3818630)			
chr22	50525751	50530084	22q13.32-qter	22q13.33		131222	"TYMP, ECGF1, MNGIE, PDECGF, MEDPS1, MTDPS1"	Thymidine phosphorylase	TYMP	1890	ENSG00000025708		"Mitochondrial DNA depletion syndrome 1 (MNGIE type), 603041 (3), Autosomal recessive"	Tymp (MGI:1920212)			
chr22	50551111	50562951	22q13.33	22q13.33		615775	SYCE3	Synaptonemal complex central element protein 3	SYCE3	644186	ENSG00000217442			Syce3 (MGI:1922709)			
chr22	50568860	50578666	22q13	22q13.33		601987	CPT1B	"Carnitine palmitoyltransferase I, muscle"	CPT1B	1375	ENSG00000205560			Cpt1b (MGI:1098297)			
chr22	50578957	50582998	22q13	22q13.33		612395	"CHKB, CHKL, CKEKB, EKB, MDCMC"	"Choline kinase, beta"	CHKB	1120	ENSG00000100288		"Muscular dystrophy, congenital, megaconial type, 602541 (3), Autosomal recessive"	Chkb (MGI:1328313)			
chr22	50600684	50613980	22q13	22q13.33		607755	"MAPK8IP2, JIP2, IB2"	Mitogen-activated protein kinase 8-interacting protein 2	MAPK8IP2	23542	ENSG00000008735			Mapk8ip2 (MGI:1926555)			
chr22	50622753	50628172	22q13.31-qter	22q13.33		607574	ARSA	Arylsulfatase A	ARSA	410	ENSG00000100299		"Metachromatic leukodystrophy, 250100 (3), Autosomal recessive"	Arsa (MGI:88077)			
chr22	50674641	50733211	22q13.3	22q13.33		606230	"SHANK3, PSAP2, PROSAP2, KIAA1650, DEL22q13.3, SCZD15"	SH3 and multiple ankyrin repeat domains 3	SHANK3	85358	ENSG00000251322		"Phelan-McDermid syndrome, 606232 (3), Autosomal dominant; {Schizophrenia 15}, 613950 (3)"	Shank3 (MGI:1930016)			
chr22	50738223	50745298	22q13.33	22q13.33		102480	ACR	Acrosin	ACR	49	ENSG00000100312		"?Male infertility due to acrosin deficiency, 102480 (2)"	Acr (MGI:87884)			
chr22	50767491	50783704	22q13.3	22q13.33		605413	RABL2B	RAB-like 2B	RABL2B	11158	ENSG00000079974						
chr22	0	50818468	Chr.22			107260	MSK41	Antigen MSK41 identified by monoclonal antibody E3									
chrX	0	24900000	Xp22			300310	"AGMX2, XLA2, IMD6"	"Agammaglobulinemia, X-linked 2 (with growth hormone deficiency)"	AGMX2	179			"Agammaglobulinemia, X-linked 2, 300310 (2), X-linked"				
chrX	0	24900000	Xp22			304050	AIC	Aicardi syndrome	AIC	192		?in p22.31 with FDH as contiguous gene syndrome	"Aicardi syndrome, 304050 (2), X-linked dominant"				
chrX	0	24900000	Xp22			300870	ANIB5	"Aneurysm, intracranial berry, 5"					"Aneurysm, intracranial berry, 5, 300870 (2)"				
chrX	0	6100000	Xpter-p22.32			301780	ARSC2	"Arylsulfatase C, f form"	ARSC2	413		"probably close to STS = ARSC1, or s form"					
chrX	0	9600000	Xp22.3			300211	EMWX	"Episodic muscle weakness, X-linked"	EMWX	10118			"Episodic muscle weakness, X-linked, 300211 (2)"				
chrX	0	9600000	Xp22.3			300406	FGS3	FG syndrome 3	FGS3	93985			"FG syndrome 3, 300406 (2)"				
chrX	0	6100000	Xpter-p22.32			300221	HDPA	"Hodgkin disease, susceptibility, pseudoautosomal"		50829			"{Hodgkin disease susceptibility, pseudoautosomal}, 300221 (2)"				
chrX	0	9600000	Xp22.3			300778	LECD	"Corneal dystrophy, Lisch epithelial"		100302509		max lod between DXYS233 and DXYS228X	"Corneal dystrophy, Lisch epithelial, 300778 (2), X-linked dominant"				
chrX	0	24900000	Xp22			300273	MNG2	Multinodular goiter-2		59081			"Goiter, multinodular, 2, 300273 (2), X-linked dominant"				
chrX	0	9600000	Xp22.3			300428	MRX2	"Mental retardation, X-linked, 2"					"Mental retardation, X-linked 2, 300428 (2), X-linked"				
chrX	0	9600000	Xp22.3			300650	OASD	Ocular albinism and sensorineural deafness	OASD	4941		?allelic to OA1	"Ocular albinism with sensorineural deafness, 300650 (2), X-linked"				
chrX	0	4400000	Xp22.33			313000	VSPA	Visuospatial/perceptual abilities		59332			"Turner syndrome-associated neurocognitive phenotype, 313000 (2), ?X-linked recessive; [Visuospatial/perceptual abilities], 313000 (2), ?X-linked recessive"				
chrX	0	6100000	Xpter-p22.32			314700	XG	Xg blood group				nonlyonizing; spans pseudoautosomal boundary; XGPY on Yq11.21	"[Blood group, XG system] (3)"				
chrX	276323	303355	Xp22.33	Xp22.33		300974	PLCXD1	"Phospholipase C, phosphatidylinositol-specific, X domain-containing protein 1"	PLCXD1	55344	ENSG00000182378	in pseudoautosomal region					
chrX	303351	318818	Xp22.33	Xp22.33		300124	"GTPBP6, PGPL"	GTP-binding protein 6	GTPBP6	8225	ENSG00000178605			Gtpbp6 (MGI:1306825)			
chrX	333932	387326	Xp22.33	Xp22.33		300339	"PPP2R3B, PR48"	"Protein phosphatase 2, regulatory subunit B-double prime, beta"	PPP2R3B	28227	ENSG00000167393						
chrX	624343	659410	Xpter-p22.32	Xp22.33		312865	"SHOX, GCFX, SS, PHOG"	Short stature homeo box	SHOX	6473	ENSG00000185960	pseudoautosomal; ?gene causing short stature in Turner syndrome	"Langer mesomelic dysplasia, 249700 (3), Autosomal recessive; Leri-Weill dyschondrosteosis, 127300 (3), Autosomal dominant; Short stature, idiopathic familial, 300582 (3)"				
chrX	1190436	1212761	Xp22.3	Xp22.33		300357	"CRLF2, CRL2"	Cytokine receptor-like factor 2	CRLF2	64109	ENSG00000205755	pseudoautosomal					
chrX	1268799	1325096	Xp22.32	Xp22.33		306250	"CSF2RA, SMDP4"	"Colony-stimulating factor-2 receptor, alpha, low-affinity, granulocyte-macrophage"	CSF2RA	1438	ENSG00000198223	order in PAR: pter-CSF2RA-IL3RA-ANT3-ASMT-MIC2-cen	"Surfactant metabolism dysfunction, pulmonary, 4, 300770 (3)"				
chrX	1336573	1382688	Xp22.3	Xp22.33		308385	IL3RA	"Interleukin-3 receptor, alpha subunit"	IL3RA	3563	ENSG00000185291	same 190kb segment as CSF2RA					
chrX	1386151	1392145	Xp22.32	Xp22.33		300151	"SLC25A6, ANT3"	"Solute carrier family 25 (mitochondrial carrier), member 6 (adenine nucleotide translocator-3, liver)"	SLC25A6	293	ENSG00000169100	1st intron ~1.3Mb from Xqter; nonlyonized					
chrX	1403138	1453793	Xpter-p22.32	Xp22.33		300162	"ASMTLX, ASTML"	Acetylserotonin methyltransferase-like	ASMTL	8623	ENSG00000169093						
chrX	1462571	1537487	Xp22.3	Xp22.33		300525	"P2RY8, P2Y8"	"Pyrimidinergic receptor P2Y, G protein-coupled, 8"	P2RY8	286530	ENSG00000182162						
chrX	1591592	1602519	Xp22.32	Xp22.33		312095	"AKAP17A, SFRS17A, DXYS155E, XE7"	A kinase (PRKA) anchor protein 17A	AKAP17A	8227	ENSG00000197976	nonlyonizing					
chrX	1595454	1643080	Xpter-p22.32	Xp22.33		300015	"ASMT, HIOMT"	Acetylserotonin methyltransferase	ASMT	438	ENSG00000196433	pseudoautosomal					
chrX	2486413	2500966	Xp22.33	Xp22.33		300178	"ZBED1, ALTE, KIAA0785, TRAMP"	Zinc finger BED domain-containing protein 1	ZBED1	9189	ENSG00000214717						
chrX	2691132	2741308	Xpter-p22.32	Xp22.33		313470	"CD99, MIC2, MIC2X"	CD99 antigen (MIC2 (monoclonal antibody 12E7))	CD99	4267	ENSG00000002586	distal to STS					
chrX	2751103	2816499	Xp22.33	Xp22.33		300879	"XG, PBDX"	XG glycoprotein	XG	7499	ENSG00000124343						
chrX	2828711	2882819	Xp22.3	Xp22.33		300198	"GYG2, GN2"	Glycogenin 2	GYG2	8908	ENSG00000056998						
chrX	2903969	2929374	Xp22.3	Xp22.33		300002	ARSD	Arylsulfatase D	ARSD	414	ENSG00000006756						
chrX	2934631	2968309	Xp22.3	Xp22.33		300180	"ARSE, CDPX1, CDPXR"	Arylsulfatase E	ARSE	415	ENSG00000157399	CDPX1 in contiguous gene syndrome with STS	"Chondrodysplasia punctata, X-linked recessive, 302950 (3), X-linked recessive"				
chrX	3006612	3033384	Xp22.3	Xp22.33		300586	ARSH	Arylsulfatase H	ARSH	347527	ENSG00000205667						
chrX	3040233	3112728	Xp22.3	Xp22.33		300003	ARSF	Arylsulfatase F	ARSF	416	ENSG00000062096						
chrX	3308564	3346642	Xp22.33	Xp22.33		300938	MXRA5	Matrix remodeling-associated protein 5	MXRA5	25878	ENSG00000101825						
chrX	3604342	3713633	Xp22.3	Xp22.33		300083	PRKX	"Protein kinase, X-linked"	PRKX	5613	ENSG00000183943			Prkx (MGI:1309999)			
chrX	4400000	6100000	Xp22.32			314705	XGR	XG/MIC2 regulator	XGR	7501		?between XG and MIC2					
chrX	5890025	6228881	Xp22.33	Xp22.32-p22.31		300427	"NLGN4, KIAA1260, AUTSX2, ASPGX2"	Neuroligin 4	NLGN4X	57502	ENSG00000146938		"{Asperger syndrome susceptibility, X-linked 2}, 300497 (3), Isolated cases, X-linked, Multifactorial; {Autism susceptibility, X-linked 2}, 300495 (3), Isolated cases, X-linked, Multifactorial; Mental retardation, X-linked, 300495 (3), Isolated cases, X-linked, Multifactorial"				
chrX	6533617	6535117	Xp22.3	Xp22.31		300533	"VCX3A, VCX8R, VCXA"	"Variably charged, X chromosome, 3A"	VCX3A	51481	ENSG00000169059						
chrX	6768839	7148189	Xp22.32	Xp22.31		306480	"HDHD1A, DXF68S1E, GS1"	Haloacid dehalogenase-like hydrolase domain-containing 1A	PUDP	8226	ENSG00000130021	escapes X-inactivation; 100kb telomeric to STS		Pudp (MGI:1914615)			
chrX	7147251	7354642	Xp22.32	Xp22.31		300747	"STS, ARSC1, ARSC, SSDD, XLI"	"Steroid sulfatase, microsomal (arylsulfatase C, isozyme S)"	STS	412	ENSG00000101846	nonlyonizing	"Ichthyosis, X-linked, 308100 (3), X-linked recessive"				
chrX	7842261	7844142	Xp22.3	Xp22.31		300229	"VCX, VCXB1, VCX10R"	"Variably charged, X chromosome"	VCX	26609	ENSG00000182583						
chrX	7898762	7928586	Xp22.3	Xp22.31		300102	DXS1283E	GS2 gene	PNPLA4	8228	ENSG00000006757						
chrX	8169943	8171266	Xp22.3	Xp22.31		300532	"VCX2, VCX2R, VCXB"	"Variably charged, X chromosome, 2"	VCX2	51480	ENSG00000177504						
chrX	8464829	8466509	Xp22.31	Xp22.31		300981	"VCS3B, VCXC"	"Variably charged, X chromosome, 3B"	VCX3B	425054	ENSG00000205642						
chrX	8528873	8732186	Xp22.3	Xp22.31		300836	"KAL1, KMS, ADMLX, HH1"	Kallmann syndrome-1 sequence (anosmin-1)	ANOS1	3730	ENSG00000011201	with ichthyosis in probable microdeletion syndrome	"Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), 308700 (3), X-linked recessive"				
chrX	8790794	8801382	Xp22.33-p22.32	Xp22.31		300477	FAM9A	"Family with sequence similarity 9, member A"	FAM9A	171482	ENSG00000183304	"pseudogene on Xq28, Yp11.31, 1p36.12, 8p11.1"					
chrX	9024231	9034126	Xp22.32	Xp22.31		300478	FAM9B	"Family with sequence similarity 9, member B"	FAM9B	171483	ENSG00000177138						
chrX	9463294	9719739	Xp22.3	Xp22.3-p22.2		300196	"TBL1X, TBL1"	"Transducin-beta-like 1, X-linked"	TBL1X	6907	ENSG00000101849			Tbl1x (MGI:1336172)			
chrX	9600000	17400000	Xp22.2			302801	CMTX2	"Charcot-Marie-Tooth disease, X-linked recessive, 2"	CMTX2	1253			"Charcot-Marie-Tooth neuropathy, X-linked recessive, 2, 302801 (2), X-linked recessive"				
chrX	9600000	17400000	Xp22.2			305435	"HBFQTL3, FCP1, FCPX, FCP"	Fetal hemoglobin quantitative trait locus 3	FCP1	2221			"Fetal hemoglobin quantitative trait locus 3, 305435 (2), X-linked"				
chrX	9600000	17400000	Xp22.2			300355	MRX73	"Mental retardation, X-linked 73"	MRX73	23694		between DXS8019 and DXS365	"Mental retardation, X-linked 73, 300355 (2), X-linked recessive"				
chrX	9725412	9786259	Xp22.3	Xp22.2		300808	"GPR143, OA1, NYS6"	G protein-coupled receptor 143	GPR143	4935	ENSG00000101850	linked to XG	"Nystagmus 6, congenital, X-linked, 300814 (3); Ocular albinism, type I, Nettleship-Falls type, 300500 (3), X-linked"	Gpr143 (MGI:107193)			
chrX	9786405	9949442	Xp22.3	Xp22.2		300103	"SHROOM2, APXL"	Shroom family member 2	SHROOM2	357	ENSG00000146950			Shroom2 (MGI:107194)			
chrX	10156944	10237659	Xp22.3	Xp22.2		302910	"CLCN4, MRX49, MRX15"	Chloride channel-4	CLCN4	1183	ENSG00000073464		"Mental retardation, X-linked 49/15, 300114 (3), X-linked recessive"	Clcn4 (MGI:104571)			
chrX	10445309	10833689	Xp22	Xp22.2		300552	"MID1, OGS1, BBBG1, FXY, OSX"	Midline-1	MID1	4281	ENSG00000101871	type II defect on chr.22	"Opitz GBBB syndrome, type I, 300000 (3), X-linked recessive"	Mid1 (MGI:1100537)			
chrX	11111285	11123085	Xp22	Xp22.2		300056	"HCCS, MCOPS7, LSDMCA1"	Holocytochrome c synthase (cytochrome c heme-lyase)	HCCS	3052	ENSG00000004961		"Linear skin defects with multiple congenital anomalies 1, 309801 (3), X-linked dominant"	Hccs (MGI:106911)			
chrX	11137542	11665700	Xp22.3	Xp22.2		300118	ARHGAP6	Rho GTPase-activating protein-6	ARHGAP6	395	ENSG00000047648			Arhgap6 (MGI:1196332)			
chrX	11293412	11304148	Xp22.3-p22.1	Xp22.2		300391	"AMELX, AMG, AIH1, AMGX, AI1E"	Amelogenin	AMELX	265	ENSG00000125363	also Y	"Amelogenesis imperfecta, type 1E, 301200 (3), X-linked dominant"				
chrX	11758158	11775752	Xp22.3	Xp22.2		300609	MSL3L1	Male-specific lethal 3-like 1	MSL3	10943	ENSG00000005302			Msl3 (MGI:1341851)			
chrX	12137328	12724522	Xp22.2	Xp22.2		300838	"FRMPD4, PRESO, KIAA0316, MRX104"	FERM and PDZ domains-containing protein 4	FRMPD4	9758	ENSG00000169933		"Mental retardation, X-linked 104, 300983 (3), X-linked recessive"	Frmpd4 (MGI:3042378)			
chrX	12791354	12824226	Xp22.3-p22.2	Xp22.2		311860	PRPS2	Phosphoribosyl pyrophosphate synthetase-2	PRPS2	5634	ENSG00000101911	between STS and ZFX		Prps2 (MGI:97776)			
chrX	12867082	12890360	Xp22.3-p22.2	Xp22.2		300365	TLR7	Toll-like receptor 7	TLR7	51284	ENSG00000196664	centromeric to TLR8		Tlr7 (MGI:2176882)			
chrX	12906619	12923168	Xp22.3-p22.2	Xp22.2		300366	TLR8	Toll-like receptor 8	TLR8	51311	ENSG00000101916	16kb telomeric to TLR7		Tlr8 (MGI:2176887)			
chrX	12975106	12977226	Xq21.3-q22	Xp22.2		300159	"TMSB4X, TMSB4, TB4X, PTMB4"	"Thymosin, beta-4, X chromosome"	TMSB4X	7114	ENSG00000205542						
chrX	13035616	13044797	Xp22.31	Xp22.2		300479	FAM9C	"Family with sequence similarity 9, member C"	FAM9C	171484	ENSG00000187268						
chrX	13318646	13320398	Xp22.2	Xp22.2		300920	ATXN3L	Ataxin 3-like	ATXN3L	92552	ENSG00000123594						
chrX	13569574	13633574	Xp22	Xp22.2		300239	EGFL6	Epidermal growth factor-like 6	EGFL6	25975	ENSG00000198759			Egfl6 (MGI:1858599)			
chrX	13689120	13709824	Xp22.2	Xp22.2		300284	RAB9	RAS-associated protein RAB9	RAB9A	9367	ENSG00000123595			Rab9 (MGI:1890695)			
chrX	13712241	13734634	Xp22.2-p22.1	Xp22.2		300202	"TRAPPC2, SEDL, SEDT"	Trafficking protein particle complex 2 (sedlin)	TRAPPC2	6399	ENSG00000196459		"Spondyloepiphyseal dysplasia tarda, 313400 (3), X-linked recessive"	Trappc2 (MGI:1913476)			
chrX	13734712	13773977	Xp22.3-p22.2	Xp22.2		300170	"OFD1, CXorf5, SGBS2, JBTS10, RP23"	OFD1 protein	OFD1	8481	ENSG00000046651	mutation identified in 1 RP23 family	"Joubert syndrome 10, 300804 (3), X-linked recessive; Orofaciodigital syndrome I, 311200 (3), X-linked dominant; ?Retinitis pigmentosa 23, 300424 (3), X-linked recessive; Simpson-Golabi-Behmel syndrome, type 2, 300209 (3), X-linked recessive"	Ofd1 (MGI:1350328)			
chrX	13770921	13938823	Xp22.2	Xp22.2		300051	"GPM6B, M6B"	Glycoprotein M6B	GPM6B	2824	ENSG00000046653			Gpm6b (MGI:107672)			
chrX	14002493	14029917	Xp22.2	Xp22.2		300962	"GEMIN8, FAM51A1"	GEM-associated protein 8	GEMIN8	54960	ENSG00000046647			Gemin8 (MGI:2384300)			
chrX	14529297	14731811	Xp22.1-p21.2	Xp22.2		305990	GLRA2	"Glycine receptor, alpha-2 polypeptide"	GLRA2	2742	ENSG00000101958			Glra2 (MGI:95748)			
chrX	14690862	14873254	Xp22.31	Xp22.2		300515	"FAAP95, FAAP90, FLJ34064, FANCB"	"Fanconi anemia-associated polypeptide, 95kD"	FANCB	2187	ENSG00000181544		"Fanconi anemia, complementation group B, 300514 (3)"	Fancb (MGI:2448558)			
chrX	15243986	15270475	Xp22.2	Xp22.2		300890	ASB9	Ankyrin repeat- and SOCS box-containing protein 9	ASB9	140462	ENSG00000102048			Asb9 (MGI:1916549)			
chrX	15281696	15315623	Xp22.31	Xp22.2		300626	ASB11	Ankyrin repeat- and SOCS box-containing protein 11	ASB11	140456	ENSG00000165192			Asb11 (MGI:1916104)			
chrX	15319450	15335553	Xp22.1	Xp22.2		311770	"PIGA, PNH1, MCAHS2"	"Phosphatidylinositol glycan, class A"	PIGA	5277	ENSG00000165195	pseudogene on chr.12	"Multiple congenital anomalies-hypotonia-seizures syndrome 2, 300868 (3), X-linked recessive; Paroxysmal nocturnal hemoglobinuria, somatic, 300818 (3)"	Piga (MGI:99461)			
chrX	15345590	15384412	Xp22.31	Xp22.2		300091	"FIGF, VEGFD"	c-fos induced growth factor (vascular endothelial growth factor D)	VEGFD	2277	ENSG00000165197			Vegfd (MGI:108037)			
chrX	15384798	15493587	Xp22.2	Xp22.2		300931	PIR	Pirin	PIR	8544	ENSG00000087842			Pir (MGI:1916906)			
chrX	15494519	15602068	Xp22	Xp22.2		300335	"ACE2, ACEH"	Angiotensin I converting enzyme 2	ACE2	59272	ENSG00000130234			Ace2 (MGI:1917258)			
chrX	15500776	15556528	Xp22.2	Xp22.2		300101	BMX	BMX non-receptor tyrosine kinase	BMX	660	ENSG00000102010			Bmx (MGI:1101778)			
chrX	15627315	15675623	Xp22	Xp22.2		300631	"TMEM27, NX17"	Transmembrane protein 27 (collectrin)	CLTRN	57393	ENSG00000147003			Tmem27 (MGI:1926234)			
chrX	15738280	15787624	Xp22.1	Xp22.2		300230	CA5B	"Carbonic anhydrase VB, mitochondrial"	CA5B	11238	ENSG00000169239			Car5b (MGI:1926249)			
chrX	15785715	15787588	Xp22.2	Xp22.2		300165	INE2	Inactivation escape 2	INE2	8551							
chrX	15790450	15826806	Xp22.1	Xp22.2		300028	"ZRSR2, U2AF1RS2"	"Zinc finger-, CCCH domain-, and RNA-binding motif-containing serine/arginine-rich protein 2"	ZRSR2	8233	ENSG00000169249			Zrsr2 (MGI:103287)			
chrX	15825805	15855013	Xp22	Xp22.2		300629	"AP1S2, MRX59, MRXSF, MRXS21, MRXS5, PGS"	"Adaptor-related protein complex 1, sigma-2 subunit"	AP1S2	8905	ENSG00000182287		"Mental retardation, X-linked syndromic 5, 304340 (3), X-linked recessive"	Ap1s2 (MGI:1889383)			
chrX	16123300	16153517	Xp22.3-p21.2	Xp22.2		305670	GRPR	Gastrin-releasing peptide receptor	GRPR	2925	ENSG00000126010			Grpr (MGI:95836)			
chrX	16167480	16172393	Xp21.3	Xp22.2		300763	MAGEB17	"Melanoma antigen, family B, 17"	MAGEB17	645864	ENSG00000182798			"Gm5071,Gm5072 (MGI:3645128,MGI:3643982)"			
chrX	16587998	16712978	Xp22	Xp22.2		300380	CTPS2	Cytidine 5-prime triphosphate synthetase 2	CTPS2	56474	ENSG00000047230			Ctps2 (MGI:1933185)			
chrX	16649786	16654673	Xp	Xp22.2		302020	"CALB3, CABP9K"	Calbindin 3 (vitamin D-dependent calcium-binding protein)	S100G	795	ENSG00000169906			S100g (MGI:104528)			
chrX	16786431	16844518	Xp22.1	Xp22.2		300677	"CXorf15, FIAT"	Chromosome X open reading frame 15	TXLNG	55787	ENSG00000086712			Txlng (MGI:3590652)			
chrX	16844649	16870410	Xp22.2	Xp22.2		300825	RBBP7	Retinoblastoma-binding protein 7	RBBP7	5931	ENSG00000102054			Rbbp7 (MGI:1194910)			
chrX	16946690	17220723	Chr.X	Xp22.2		300317	"REPS2, POB1"	RALBP1-associated EPS domain-containing protein 2	REPS2	9185	ENSG00000169891			Reps2 (MGI:2663511)			
chrX	17375419	17735993	Xp22.13	Xp22.2-p22.1		300457	"NHS, CXN, CTRCT40"	NHS gene	NHS	4810	ENSG00000188158		"Cataract 40, X-linked, 302200 (3), X-linked; Nance-Horan syndrome, 302350 (3), X-linked dominant"	Nhs (MGI:2684894)			
chrX	17400000	37800000	Xp22.13-p21.1			300148	MEHMO	"MEHMO syndrome (Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity)"					"MEHMO syndrome, 300148 (2)"				
chrX	17737448	17754987	Xp22.2-p22.1	Xp22.13		300227	SCML1	"Sex comb on midleg, Drosophila, homolog-like 1"	SCML1	6322	ENSG00000047634						
chrX	17800048	17861345	Xp22	Xp22.13		300217	RAI2	Retinoic acid-induced 2	RAI2	10742	ENSG00000131831			Rai2 (MGI:1344378)			
chrX	18239312	18355088	Xp22	Xp22.13		300208	SCML2	"Sex comb on midleg, Drosophila, homolog-like 2"	SCML2	10389	ENSG00000102098						
chrX	18425604	18653628	Xp22	Xp22.13		300203	"CDKL5, STK9, ISSX, EIEE2"	Cyclin-dependent kinase-like 5 (serine/threonine protein kinase 9)	CDKL5	6792	ENSG00000008086		"Epileptic encephalopathy, early infantile, 2, 300672 (3), X-linked dominant"	Cdkl5 (MGI:1278336)			
chrX	18639687	18672102	Xp22.2-p22.1	Xp22.13		300839	"RS1, XLRS1"	Retinoschisin	RS1	6247	ENSG00000102104	25cM from XG	"Retinoschisis, 312700 (3), X-linked recessive"	Rs1 (MGI:1336189)			
chrX	18675908	18827920	Xp22.2-p22.1	Xp22.13		300109	PPEF1	"Protein phosphatase, EF hand calcium-binding domain 1"	PPEF1	5475	ENSG00000086717			Ppef1 (MGI:1097157)			
chrX	18892297	18984361	Xp22.2-p22.1	Xp22.13		300798	"PHKA2, PHK, XLG, PYKL, GSD9A"	"Phosphorylase kinase, liver, alpha-2 subunit"	PHKA2	5256	ENSG00000044446		"Glycogen storage disease, type IXa1, 306000 (3), X-linked recessive; Glycogen storage disease, type IXa2, 306000 (3), X-linked recessive"	Phka2 (MGI:97577)			
chrX	18989306	19122955	Xp21.3	Xp22.13		300572	"ADGRG2, GPR64, HE6, CBAVDX"	Adhesion G protein-coupled receptor G2	ADGRG2	10149	ENSG00000173698		"Vas deferens, congenital bilateral aplasia of, X-linked, 300985 (3), X-linked"	Adgrg2 (MGI:2446854)			
chrX	19343892	19361706	Xp22.2-p22.1	Xp22.12		300502	"PDHA1, PHE1A, PDHAD"	"Pyruvate dehydrogenase, E1-alpha polypeptide-1"	PDHA1	5160	ENSG00000131828		"Pyruvate dehydrogenase E1-alpha deficiency, 312170 (3), X-linked dominant"	Pdha1 (MGI:97532)			
chrX	19360057	19515260	Xp22.12	Xp22.12		300820	"MAP3K15, ASK3"	Mitogen-activated protein kinase kinase kinase 15	MAP3K15	389840	ENSG00000180815			Map3k15 (MGI:2448588)			
chrX	19533964	19887625	Xp22.1-p21.3	Xp22.12		300374	"SH3KBP1, CIN85"	SH3-domain kinase-binding protein 1	SH3KBP1	30011	ENSG00000147010			Sh3kbp1 (MGI:1889583)			
chrX	20124517	20141847	Chr.X	Xp22.12		300186	"EIF1A, EIF4C, EIF1AX"	Eukaryotic translation initiation factor 1A	EIF1AX	1964	ENSG00000173674			Eif1a (MGI:95298)			
chrX	20149910	20267513	Xp22.2-p22.1	Xp22.12		300075	"RPS6KA3, RSK2, MRX19"	"Ribosomal protein S6 kinase, 90kD, polypeptide 3"	RPS6KA3	6197	ENSG00000177189		"Coffin-Lowry syndrome, 303600 (3), X-linked dominant, Isolated cases; Mental retardation, X-linked 19, 300844 (3), X-linked dominant"	Rps6ka3 (MGI:104557)			
chrX	21374297	21654694	Xp22.12	Xp22.12		300724	"CNKSR2, CNK2, KIAA0902, MRXSHG"	connector enhancer of KSR 2	CNKSR2	22866	ENSG00000149970	conflicting assignment to chr.1	"Mental retardation, X-linked, syndromic, Houge type, 301008 (3), X-linked"	Cnksr2 (MGI:2661175)			
chrX	21705971	21758159	Xp22.1	Xp22.12		300226	"SMPX, DFNX4"	"Small muscle protein, X-linked"	SMPX	23676	ENSG00000091482		"Deafness, X-linked 4, 300066 (3), X-linked dominant"				
chrX	21839537	21885422	Xp22.12-p22.11	Xp22.12		300294	"MBTPS2, S2P, IFAP, KFSDX, OLMSX"	"Membrane-bound transcription factor protease, site 2"	MBTPS2	51360	ENSG00000012174	mutation identified in 1 OLMSX family	"IFAP syndrome with or without BRESHECK syndrome, 308205 (3), X-linked recessive; Keratosis follicularis spinulosa decalvans, X-linked, 308800 (3), X-linked recessive; ?Olmsted syndrome, X-linked, 300918 (3), X-linked recessive"	Mbtps2 (MGI:2444506)			
chrX	21855986	21858726	Xp22.2-p22.1	Xp22.12		300570	"YY2, ZNF631"	Transcription factor YY2	YY2	404281	ENSG00000230797			Yy2 (MGI:3837947)			
chrX	21940572	21994836	Xp22.1	Xp22.11		300105	"SMS, SRS, MRSR"	Spermine synthase	SMS	6611	ENSG00000102172		"Mental retardation, X-linked, Snyder-Robinson type, 309583 (3), X-linked recessive"	"Sms-ps,Sms (MGI:109490,MGI:3705601)"			
chrX	22032326	22251309	Xp22.2-p22.1	Xp22.11		300550	"PHEX, HYP, HPDR1, LXHR"	"Phosphate regulating endopeptidase homolog, X-linked"	PHEX	5251	ENSG00000102174		"Hypophosphatemic rickets, X-linked dominant, 307800 (3), X-linked dominant"	Phex (MGI:107489)			
chrX	23334368	23404373	Xp22.11	Xp22.11		300828	"PTCHD1, AUTSX4"	Patched domain-containing protein 1	PTCHD1	139411	ENSG00000165186		"{Autism, susceptibility to, X-linked 4}, 300830 (3), X-linked recessive"	Ptchd1 (MGI:2685233)			
chrX	23664259	23686398	Xp22.11	Xp22.11		300927	"PRDX4, AOE372"	Peroxiredoxin 4	PRDX4	10549	ENSG00000123131			Prdx4 (MGI:1859815)			
chrX	23701054	23743289	Xp22.11	Xp22.11		300862	"ACOT9, MTACT48"	Acyl-CoA thioesterase 9	ACOT9	23597	ENSG00000123130			"Acot9,Acot10 (MGI:1928939,MGI:1928940)"			
chrX	23783157	23786222	Xp22.1	Xp22.11		313020	"SAT1, SSAT"	Spermidine/spermine N1-acetyltransferase 1	SAT1	6303	ENSG00000130066			Sat1 (MGI:98233)			
chrX	23833347	23907939	Xp22.1	Xp22.11		300753	"APOO, MYO25, FAM121B"	Apolipoprotein O	APOO	79135	ENSG00000184831			Apoo (MGI:1915566)			
chrX	23983715	24027185	Xp22.1	Xp22.11		300980	"KLHL15, KIAA1677"	Kelch-like 15	KLHL15	80311	ENSG00000174010		"Mental retardation, X-linked 103, 300982 (3), X-linked recessive"	Klhl15 (MGI:1923400)			
chrX	24054947	24078809	Xp22.2-p22.1	Xp22.11		300161	"EIF2S3, EIF2G, MEHMO, MRXSBRK"	"Eukaryotic translation initiation factor 2, subunit 3"	EIF2S3	1968	ENSG00000130741		"MEHMO syndrome, 300148 (3)"	Eif2s3x (MGI:1349431)			
chrX	24148988	24216254	Xp22.2-p21.3	Xp22.11		314980	ZFX	"Zinc finger protein, X-linked"	ZFX	7543	ENSG00000005889	nonlyonizing		Zfx (MGI:99211)			
chrX	24465226	24550465	Xp22.11	Xp22.11		300906	"PDK3, CMTX6"	"Pyruvate dehydrogenase kinase, isoenzyme 3"	PDK3	5165	ENSG00000067992	1 family identified with mutation	"?Charcot-Marie-Tooth disease, X-linked dominant, 6, 300905 (3), X-linked dominant"	Pdk3 (MGI:2384308)			
chrX	24558086	24672861	Xp22.11	Xp22.11		300948	PCYT1B	"Phosphate cytidylyltransferase 1, choline, beta isoform"	PCYT1B	9468	ENSG00000102230			Pcyt1b (MGI:2147987)			
chrX	24693832	24996985	Xp22.3-p21.1	Xp22.1-p21.3		312040	POLA1	"Polymerase, DNA, alpha-1"	POLA1	5422	ENSG00000101868		"Pigmentary disorder, reticulate, with systemic manifestations, X-linked, 301220 (3), X-linked recessive"	Pola1 (MGI:99660)			
chrX	24900000	37800000	Xp21			300679	"DELXp21, CXDELp21"	Chromosome Xp21 deletion syndrome				contiguous gene deletion syndrome	"Chromosome Xp21 deletion syndrome, 300679 (4)"				
chrX	24900000	29300000	Xp21.3			300488	MENOQ1	"Menopause, natural, age at, QTL 1"		494029			"{Menopause, natural, age at, QTL1}, 300488 (2), X-linked dominant"				
chrX	24900000	31500000	Xp21.3-p21.2			312612	RP6	"Retinitis pigmentosa-6, X-linked recessive"	RP6	6104			"?Retinitis pigmentosa, X-linked recessive, 6, 312612 (2), X-linked"				
chrX	25003693	25015947	Xp22.13	Xp21.3		300382	"ARX, ISSX, PRTS, MRXS1, MRX36, MRX54, MRX43, MRX87, MRX29, MRX32"	"Aristaless-related homeobox, X-linked"	ARX	170302	ENSG00000004848		"Epileptic encephalopathy, early infantile, 1, 308350 (3), X-linked recessive; Hydranencephaly with abnormal genitalia, 300215 (3), X-linked; Lissencephaly, X-linked 2, 300215 (3), X-linked; Mental retardation, X-linked 29 and others, 300419 (3), X-linked recessive; Partington syndrome, 309510 (3), X-linked recessive; Proud syndrome, 300004 (3), X-linked"	Arx (MGI:1097716)			
chrX	26192439	26195645	Xp22	Xp21.3		300467	MAGEB6	"Melanoma antigen, family B, 6"	MAGEB6	158809	ENSG00000176746						
chrX	26216168	26218269	Xp22	Xp21.3		300466	MAGEB5	"Melanoma antigen, family B, 5"	MAGEB5	347541	ENSG00000188408			"Gm14781,Mageb5 (MGI:2148169,MGI:3712084)"			
chrX	27807989	27823013	Xp21.3	Xp21.3		300761	MAGEB10	"Melanoma antigen, family B, 10"	MAGEB10	139422	ENSG00000177689						
chrX	28587563	29956349	Xp22.1-p21.3	Xp21.3-p21.2		300206	"IL1RAPL1, IL1R8, MRX21, MRX34"	Il-1 receptor accessory protein-like 1	IL1RAPL1	11141	ENSG00000169306		"Mental retardation, X-linked 21/34, 300143 (3), X-linked recessive"	Il1rapl1 (MGI:2687319)			
chrX	29300000	31500000	Xp21.2			300030	"DFNX3, DFN4"	"Deafness, X-linked 3"	DFNX3	1680		?same as DMD	"Deafness, X-linked 3, 300030 (2), X-linked"				
chrX	29300000	85400000	Xp21.2-q21.1			309050	"XS, LUXS"	"Lutheran suppressor, X-linked"	XS	7523							
chrX	30215557	30220088	Xp21.3	Xp21.2		300098	"MAGEB2, DAM6"	"Melanoma antigen, family B, 2"	MAGEB2	4113	ENSG00000099399			Mageb4 (MGI:2148568)			
chrX	30230435	30237492	Xp21.3	Xp21.2		300152	MAGEB3	"Melanoma antigen, family B, 3"	MAGEB3	4114	ENSG00000198798						
chrX	30241939	30244192	Xp21.3	Xp21.2		300153	MAGEB4	"Melanoma antigen, family B, 4"	MAGEB4	4115	ENSG00000120289						
chrX	30243730	30252037	Xp21.3	Xp21.2		300097	"MAGEB1, MAGEL1, DAM10"	"Melanoma antigen, family B, 1"	MAGEB1	4112	ENSG00000214107			"Mageb1,Mageb2,Mageb3 (MGI:105109,MGI:105118,MGI:105117)"			
chrX	30304421	30309377	Xp21.3-p21.2	Xp21.2		300473	"NR0B1, DAX1, AHC, AHX, SRXY2"	"Nuclear receptor subfamily 0, group B, member 1"	NR0B1	190	ENSG00000169297	distal to GK	"Adrenal hypoplasia, congenital, 300200 (3), X-linked recessive; 46XY sex reversal 2, dosage-sensitive, 300018 (3), X-linked"	Nr0b1 (MGI:1352460)			
chrX	30653347	30731461	Xp21.3-p21.2	Xp21.2		300474	GK	Glycerol kinase	GK	2710	ENSG00000198814	2Mb distal to DMD; pseudogene on 4q32	"Glycerol kinase deficiency, 307030 (3), X-linked recessive"	Gykl1 (MGI:891990)			
chrX	30827441	30889393	Xp21.2	Xp21.2		300480	TAB3	Tak1 (MAP3K7) binding protein 3	TAB3	257397	ENSG00000157625			Tab3 (MGI:1913974)			
chrX	31071240	31072052	Xp21.2	Xp21.2		300308	FTHL17	Ferritin heavy polypeptide-like 17	FTHL17	53940	ENSG00000132446						
chrX	31119218	33339608	Xp21.2	Xp21.2-p21.1		300377	"DMD, BMD, CMD3B"	Dystrophin	DMD	1756	ENSG00000198947	dystrophin gene; cen-5'-3'-pter; 2Mb; ?Xp21.13	"Becker muscular dystrophy, 300376 (3), X-linked recessive; Cardiomyopathy, dilated, 3B, 302045 (3), X-linked; Duchenne muscular dystrophy, 310200 (3), X-linked recessive"	Dmd (MGI:94909)			
chrX	31500000	50100000	Xp21.1-p11.23			300858	MRXS17	"Mental retardation, X-linked, syndromic 17"		100739996		between rs2748314 and rs5906782	"Mental retardation, X-linked, syndromic 17, 300858 (2), X-linked recessive"				
chrX	34627063	34657287	Xp11.4	Xp21.1		300698	"TMEM47, BCMP1"	Transmembrane protein 47	TMEM47	83604	ENSG00000147027			Tmem47 (MGI:2177570)			
chrX	35798310	35803771	Xp21.3	Xp21.1		300762	MAGEB16	"Melanoma antigen, family B, 16"	MAGEB16	139604	ENSG00000189023			Mageb16 (MGI:1919217)			
chrX	37349274	37457294	Xp21.1	Xp21.1		300935	"PRRG1, PRGP1"	Proline-rich gamma-carboxyglutamic acid protein 1	PRRG1	5638	ENSG00000130962			Prrg1 (MGI:1917364)			
chrX	37685685	37732129	Xp21.2-p21.1	Xp21.1		314850	"XK, MCLDS"	Kell blood group precursor	XK	7504	ENSG00000047597	~500kb distal to CGD	"McLeod syndrome with or without chronic granulomatous disease, 300842 (3), X-linked"	Xk (MGI:103569)			
chrX	37780016	37813460	Xp21.1	Xp21.1-p11.4		300481	"CYBB, CGD, AMCBX2, IMD34"	"Cytochrome b-245, beta polypeptide"	CYBB	1536	ENSG00000165168	proximal to DMD	"Chronic granulomatous disease, X-linked, 306400 (3), X-linked recessive; Immunodeficiency 34, mycobacteriosis, X-linked, 300645 (3), X-linked recessive"	Cybb (MGI:88574)			
chrX	37800000	58100000	Xp11.4-p11.2			300638	GAGE8	G antigen 8	GAGE8	100101629	ENSG00000189064						
chrX	37800000	61000000	Xp11			300351	"GRDX, GD3"	"Graves disease, susceptibility to, X-linked"		117189			"{Graves disease, susceptibility to, X-linked}, 300351 (2)"				
chrX	37800000	61000000	Xp11			300136	IDDMX	"Diabetes mellitus, insulin-dependent, X-linked, susceptibility to"		8245		only with DR3	"{Diabetes mellitus, insulin-dependent, X-linked}, 300136 (2)"				
chrX	37800000	61000000	Xp11			308905	LOAS	"Leber optic atrophy, susceptibility to"		100188775			"{Leber optic atrophy, susceptibility to}, 308905 (2), X-linked"				
chrX	37800000	99100000	Xp11-q21			300047	MRX20	"Mental retardation, X-linked-20"	MRX20	4384			"Mental retardation, X-linked 20, 300047 (2), X-linked"				
chrX	37800000	61000000	Xp11			309545	MRXS12	"Mental retardation, X-linked, syndromic 12"		8246			"?Mental retardation, X-linked, syndromic 12, 309545 (2), X-linked"				
chrX	37800000	42500000	Xp11.4			300589	NYS5	"Nystagmus 5, congenital, X-linked"		780901		max lod at DXS993	"Nystagmus 5, congenital, X-linked, 300589 (2), X-linked dominant"				
chrX	37800000	58100000	Xp11.4-p11.21			311050	OPA2	"Optic atrophy, X-linked"	OPA2	4977			"Optic atrophy 2, X-linked, 311050 (2), X-linked"				
chrX	37800000	99100000	Xp11-q21			309610	"PRS, MRXS2"	"Prieto syndrome (mental retardation, X-linked, syndromic 2, with dysmorphism and cerebral atrophy)"	PRS	5640			"Prieto syndrome, 309610 (2), X-linked recessive"				
chrX	37838835	37847635	Xp21	Xp11.4		300302	TCTE1L	T complex-associated testis-expressed 1-like	DYNLT3	6990	ENSG00000165169			Dynlt3 (MGI:1914367)			
chrX	38149334	38220923	Xp21.1	Xp11.4		300187	"SRPX, ETX1"	"Sushi-repeat-containing protein, X chromosome"	SRPX	8406	ENSG00000101955	probably between OTC and CGD		Srpx (MGI:1858306)			
chrX	38269162	38327541	Xp11.4	Xp11.4		312610	"RPGR, RP3, CRD, RP15, COD1, CORDX1"	Retinitis pigmentosa GTPase regulator	RPGR	6103	ENSG00000156313		"Cone-rod dystrophy, X-linked, 1, 304020 (3), X-linked; Macular degeneration, X-linked atrophic, 300834 (3), X-linked recessive; Retinitis pigmentosa 3, 300029 (3); Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness, 300455 (3)"	Rpgr (MGI:1344037)			
chrX	38352482	38421449	Xp21.1	Xp11.4		300461	OTC	Ornithine transcarbamylase	OTC	5009	ENSG00000036473	"proximal to DMD, CGD"	"Ornithine transcarbamylase deficiency, 311250 (3), X-linked recessive"	Otc (MGI:97448)			
chrX	38561477	38688917	Xq11	Xp11.4		300096	"TSPAN7, TM4SF2, MXS1, A15, MRX58"	Tetraspanin 7	TSPAN7	7102	ENSG00000156298		"Mental retardation, X-linked 58, 300210 (3), X-linked recessive"	Tspan7 (MGI:1298407)			
chrX	38801431	38806531	Xp11.4	Xp11.4		300961	"MID1IP1, MIG12"	MID1-interacting protein 1	MID1IP1	58526	ENSG00000165175			Mid1ip1 (MGI:1915291)			
chrX	40051245	40177389	Xp11.4	Xp11.4		300485	"BCOR, KIAA1575, MCOPS2, MAA2, ANOP2"	BCL6 corepressor	BCOR	54880	ENSG00000183337		"Microphthalmia, syndromic 2, 300166 (3), X-linked dominant"	Bcor (MGI:1918708)			
chrX	40580963	40606636	Xp11.4	Xp11.4		300556	"ATP6AP2, ATP6M8-9, XMRE, MRXSH, XPDS"	"ATPase, H+ transporting, lysosomal, accessory protein 2"	ATP6AP2	10159	ENSG00000182220	mutation identified in 1 XPDS family	"Mental retardation, X-linked, syndromic, Hedera type, 300423 (3), X-linked recessive; ?Parkinsonism with spasticity, X-linked, 300911 (3), X-linked recessive"	Atp6ap2 (MGI:1917745)			
chrX	40649542	40736121	Xp11.4-p11.2	Xp11.4		300182	"MED14, CRSP2, CXorf4, TRAP170, EXLM1"	Mediator complex subunit 14	MED14	9282	ENSG00000180182			Med14 (MGI:1349442)			
chrX	41085419	41236578	Xp11.4	Xp11.4		300072	"USP9X, DFFRX, MRX99, MRXS99F"	"Ubiquitin-specific protease-9, X chromosome (Drosophila fat facets related, X-linked)"	USP9X	8239	ENSG00000124486		"Mental retardation, X-linked 99, 300919 (3), X-linked recessive; Mental retardation, X-linked 99, syndromic, female-restricted, 300968 (3), X-linked dominant"	Usp9x (MGI:894681)			
chrX	41333307	41364471	Xp11.3-p11.23	Xp11.4		300160	"DDX3X, DDX3, DBX, MRX102"	"DEAD/H box-3, X-linked"	DDX3X	1654	ENSG00000215301		"Mental retardation, X-linked 102, 300958 (3), X-linked recessive, X-linked dominant"	Ddx3x (MGI:103064)			
chrX	41447459	41476413	Xp11.4	Xp11.4		300278	"NYX, CSNB1A, NBM1"	Nyctalopin	NYX	60506	ENSG00000188937		"Night blindness, congenital stationary (complete), 1A, X-linked, 310500 (3), X-linked recessive"	Nyx (MGI:2448607)			
chrX	41514933	41923524	Xp11.4	Xp11.4		300172	"CASK, MICPCH, FGS4, CMG, MRXSNA"	Calcium/calmodulin-dependent serine protein kinase	CASK	8573	ENSG00000147044		"FG syndrome 4, 300422 (3); Mental retardation and microcephaly with pontine and cerebellar hypoplasia, 300749 (3), X-linked dominant; Mental retardation, with or without nystagmus, 300422 (3)"	Cask (MGI:1309489)			
chrX	41686396	41697276	Xp11.4	Xp11.4		300241	GPR34	G protein-coupled receptor 34	GPR34	2857	ENSG00000171659			Gpr34 (MGI:1346334)			
chrX	41724154	41730134	Xp11.4	Xp11.4		300748	GPR82	G protein-coupled receptor 82	GPR82	27197	ENSG00000171657			Gpr82 (MGI:2441734)			
chrX	42500000	68500000	Xp11.3-q12			300652	AGSPX	"Angioma serptiginosum, X-linked"		100188767		between DXS8026 and DXS106	"Angio serpiginosum, 300652 (2), X-linked dominant"				
chrX	42500000	47600000	Xp11.3			300578	"DELXp11.3, CXDELp11.3"	Chromosome Xp11.3 deletion syndrome (X-linked mental retardation with retinitis pigmentosa)					"Chromosome Xp11.3 deletion syndrome, 300578 (4), X-linked recessive"				
chrX	42500000	76800000	Xp11.3-q13.3			300062	MRX14	"Mental retardation, X-linked-14"	MRX14	4378			"Mental retardation, X-linked 14, 300062 (2), X-linked"				
chrX	42500000	58100000	Xp11.3-p11.21			300498	MRX45	"Mental retardation, X-linked 45"					"Mental retardation,X-linked 45, 300498 (2), X-linked"				
chrX	42500000	58100000	Xp11.3-p11.21			300115	MRX50	"Mental retardation, X-linked nonspecific, type 50"	MRX50	4413			"Mental retardation, X-linked 50, 300115 (2), X-linked"				
chrX	42500000	109400000	Xp11.3-q22.3			300505	MRX84	"Mental retardation, X-linked 84"	MRX84	378882		29 other MRX loci in same region	"Mental retardation, X-linked 84, 300505 (2), X-linked recessive"				
chrX	42500000	47600000	Xp11.3			300848	MRX89	"Mental retardation, X-linked 89"				t(X;7)(p11.3;q11.21)	"Mental retardation, X-linked 89, 300848 (2), X-linked dominant"				
chrX	42500000	47600000	Xp11.3			300851	MRX92	"Mental retardation, X-linked 92"		102775565		previously associated with ZNF674	"Mental retardation, X-linked 92, 300851 (2), X-linked recessive"				
chrX	42500000	109400000	Xp11.3-q22			300218	MRXS7	"Mental retardation, X-linked, syndromic 7"	MRXS7	4429			"Mental retardation, X-linked syndromic 7, 300218 (2)"				
chrX	43654906	43746823	Xp11.23	Xp11.3		309850	"MAOA, BRNRS"	Monoamine oxidase A	MAOA	4128	ENSG00000189221	"NDP, MAOA, MAOB closely linked"	"{Antisocial behavior}, 300615 (3), X-linked recessive; Brunner syndrome, 300615 (3), X-linked recessive"	Maoa (MGI:96915)			
chrX	43766609	43882474	Xp11.23	Xp11.3		309860	MAOB	Monoamine oxidase B	MAOB	4129	ENSG00000069535			Maob (MGI:96916)			
chrX	43948775	43973674	Xp11.4	Xp11.3		300658	"NDP, ND, EVR2"	Norrin	NDP	4693	ENSG00000124479		"Exudative vitreoretinopathy 2, X-linked, 305390 (3); Norrie disease, 310600 (3), X-linked recessive"	Ndp (MGI:102570)			
chrX	44146253	44343676	Xp11.3	Xp11.3		300817	EFHC2	EF-hand domain (C-terminal)-containing protein 2	EFHC2	80258	ENSG00000183690			Efhc2 (MGI:1921655)			
chrX	44523638	44542974	Xp11.3	Xp11.3		300871	FUNDC1	FUN14 domain-containing protein 1	FUNDC1	139341	ENSG00000069509			Fundc1 (MGI:1919268)			
chrX	44844002	44844887	Xp11.3	Xp11.3		300678	"DUSP21, LMWDSP21"	Dual-specificity phosphatase 21	DUSP21	63904	ENSG00000189037						
chrX	44873174	45112611	Xp11.2	Xp11.3		300128	"KDM6A, UTX, KABUK2"	Lysine (K)-specific demethylase 6A	KDM6A	7403	ENSG00000147050	UTY also in mouse and man; escapes inactivation	"Kabuki syndrome 2, 300867 (3), X-linked dominant"	Kdm6a (MGI:1095419)			
chrX	45148372	45200900	Xp11.3	Xp11.3		300959	"CXorf36, DIA1R"	Chromosome X open reading frame 36	CXorf36	79742	ENSG00000147113			4930578C19Rik (MGI:1923155)			
chrX	45746156	45746265	Xp11.3	Xp11.3		300568	"MIR221, MIRN221"	Micro RNA 221	MIR221	407006		near MIRN222					
chrX	45747014	45747123	Xp11.3	Xp11.3		300569	"MIR222, MIRN222"	Micro RNA 222	MIR222	407007		near MIRN221					
chrX	46447188	46474638	Xp11.3	Xp11.3		300585	"ZNF673, FLJ20344"	Zinc finger protein 673	KRBOX4	55634	ENSG00000147121						
chrX	46497724	46545465	Xp11	Xp11.3		300573	ZNF674	Zinc finger protein 674	ZNF674	641339	ENSG00000251192						
chrX	46573686	46598495	Xp11.3	Xp11.3		300375	"CHST7, C6ST2"	Carbohydrate sulfotransferase 7	CHST7	56548	ENSG00000147119			Chst7 (MGI:1891767)			
chrX	46599250	46759171	Xp11.3	Xp11.3		300368	"SLC9A7, NHE7"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 7"	SLC9A7	84679	ENSG00000065923			Slc9a7 (MGI:2444530)			
chrX	46836911	46882357	Xp11.23	Xp11.3		300757	RP2	"Retinitis pigmentosa-2, X-linked recessive"	RP2	6102	ENSG00000102218		"Retinitis pigmentosa 2, 312600 (3), X-linked"	Rp2 (MGI:1277953)			
chrX	46912275	47061241	Xp11.23	Xp11.3		300618	"PHF16, JADE3, KIAA0215"	PHD finger protein 16	JADE3	9767	ENSG00000102221			Jade3 (MGI:2148019)			
chrX	47078354	47093313	Xp11.2-q11.2	Xp11.3		300212	"RGN, SMP30"	Regucalcin	RGN	9104	ENSG00000130988			Rgn (MGI:108024)			
chrX	47142215	47145209	Xp11.3	Xp11.3		300403	"NDUFB11, LSDMCA3"	"NADH-dehydrogenase 1 beta subcomplex, 11"	NDUFB11	54539	ENSG00000147123	mutation identified in 1 COX I deficient patient	"Linear skin defects with multiple congenital anomalies 3, 300952 (3), X-linked dominant; ?Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufb11 (MGI:1349919)			
chrX	47145195	47186814	Xp11.23	Xp11.3		300080	"RBM10, DXS8237E, KIAA0122, TARPS"	RNA-binding motif protein 10	RBM10	8241	ENSG00000182872		"TARP syndrome, 311900 (3), X-linked recessive"	Rbm10 (MGI:2384310)			
chrX	47190799	47215127	Xp11.23	Xp11.3		314370	"UBA1, UBE1, GXP1, A1ST, SMAX2, AMCX1"	Ubiquitin-like modifier-activating enzyme 1	UBA1	7317	ENSG00000130985	escapes inactivation	"Spinal muscular atrophy, X-linked 2, infantile, 301830 (3), X-linked recessive"	Uba1 (MGI:98890)			
chrX	47204847	47205860	Xp11.23	Xp11.3		300164	INE1	Inactivation escape 1	INE1	8552							
chrX	47217880	47229996	Xp11.3-p11.23	Xp11.3		311550	"CDK16, PCTK1, PCTAIRE1"	Cyclin-dependent kinase 16	CDK16	5127	ENSG00000102225			Cdk16 (MGI:97516)			
chrX	47232914	47248327	Xp21.2-p11.2	Xp11.3		300050	"USP11, UHX1"	Ubiquitin-specific protease-11 (ubiquitin carboxyl-terminal hydrolase)	USP11	8237	ENSG00000102226			Usp11 (MGI:2384312)			
chrX	47370599	47413698	Xp11.2	Xp11.3		300024	ZNF157	Zinc finger protein-157 (HZF22)	ZNF157	7712	ENSG00000147117						
chrX	47444690	47485933	Xp22.1-cen	Xp11.3		314995	ZNF41	Zinc finger protein-41	ZNF41	7592	ENSG00000147124						
chrX	47561099	47571920	Xp11.4-p11.2	Xp11.3		311010	"ARAF1, RAFA1, PKS2"	Oncogene ARAF1	ARAF	369	ENSG00000078061			Araf (MGI:88065)			
chrX	47571900	47619856	Xp11.4-p11.2	Xp11.3-p11.2		313440	SYN1	Synapsin I	SYN1	6853	ENSG00000008056	5kb from PFC	"Epilepsy, X-linked, with variable learning disabilities and behavior disorders, 300491 (3), X-linked recessive, X-linked dominant"	Syn1 (MGI:98460)			
chrX	47582290	47586790	Xp11.3-p11.23	Xp11.3		305370	"TIMP1, TIMP, EPA"	Erythroid-potentiating activity (tissue inhibitor of metalloproteinases)	TIMP1	7076	ENSG00000102265	in intron of SYN1		Timp1 (MGI:98752)			
chrX	47600000	54800000	Xp11.23-p11.22			300801	"DUPXp11.23p11.22, CXDUPp11.23p11.22"	Chromosome Xp11.23-p11.22 duplication syndrome					"Chromosome Xp11.23-p11.22 duplication syndrome, 300801 (4), X-linked dominant"				
chrX	47600000	50100000	Xp11.23			300726	GAGE2B	G antigen 2B	GAGE2B	645037	ENSG00000189064						
chrX	47600000	50100000	Xp11.23			300595	"GAGE2C, GAGE2"	G antigen 2C	GAGE2C	2574	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300735	GAGE2D	G antigen 2D	GAGE2D	729408	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300736	GAGE2E	G antigen 2E	GAGE2E	26749	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300596	GAGE3	G antigen 3									
chrX	47600000	50100000	Xp11.23			300597	GAGE4	G antigen 4	GAGE4	2576	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300598	GAGE5	G antigen 5	GAGE5	2577							
chrX	47600000	50100000	Xp11.23			300599	GAGE6	G antigen 6	GAGE6	2578	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300601	GAGE7	G antigen 7	GAGE7	2579	ENSG00000236362						
chrX	47600000	50100000	Xp11.23			300637	GAGE7B	G antigen 7B	GAGE12I	26748	ENSG00000236362						
chrX	47600000	68500000	Xp11.2-q12			300433	MRX81	"Mental retardation, X-linked 81"	MRX81	266678		between DXS1039 and DXS1216	"Mental retardation, X-linked 81, 300433 (2), X-linked recessive"				
chrX	47624212	47630304	Xp11.4-p11.23	Xp11.23		300383	"PFC, PFD"	"Properdin P factor, complement"	CFP	5199	ENSG00000126759		"Properdin deficiency, X-linked, 312060 (3), X-linked recessive"	Cfp (MGI:97545)			
chrX	47635519	47650603	Xp11.2	Xp11.23		311040	ELK1	"ELK1, member of ETS oncogene family"	ELK1	2002	ENSG00000126767	distal to OATL1		Elk1 (MGI:101833)			
chrX	47651791	47659179	Xp11.23	Xp11.23		300234	UXT	Ubiquitously expressed transcript	UXT	8409	ENSG00000126756			Uxt (MGI:1277988)			
chrX	47836863	47925625	Xp22.1-p11	Xp11.23		314998	ZNF81	Zinc finger protein-81 (HFZ20)	ZNF81	347344	ENSG00000197779						
chrX	47974850	48003994	Xp11.3	Xp11.23		314993	ZNF21	Zinc finger protein-12	ZNF182	7569	ENSG00000147118			Zfp182 (MGI:2442220)			
chrX	48004335	48009735	Xp11.23	Xp11.23		300593	"SPACA5, LOC389852"	Sperm acrosome associated 5	SPACA5	389852	ENSG00000171489			Spaca5 (MGI:2685564)			
chrX	48058177	48071657	Xp11.23	Xp11.23		300819	ZNF630	Zinc finger protein 630	ZNF630	57232	ENSG00000221994						
chrX	48107981	48120685	Xp11.23	Xp11.23		300541	SSX6	"Synovial sarcoma, X breakpoint 6"	SSX6	280657							
chrX	48177981	48196797	Xp11.23	Xp11.23		300327	SSX5	"Synovial sarcoma, X breakpoint 5"	SSX5	6758	ENSG00000165583						
chrX	48255316	48267443	Xp11.23	Xp11.23		312820	"SSX1, SSRC"	"Synovial sarcoma, X breakpoint 1"	SSX1	6756	ENSG00000126752	fused with SYT in synovial sarcoma	"?Sarcoma, synovial, 300813 (3)"				
chrX	48301549	48306178	Xp11.23	Xp11.23		300544	SSX9	"Sarcoma, synovial, X breakpoint 9"	SSX9	280660							
chrX	48346427	48356752	Xp11.23	Xp11.23		300325	SSX3	"Synovial sarcoma, X breakpoint 3"	SSX3	10214	ENSG00000165584						
chrX	48383526	48393342	Xp11.23	Xp11.23		300326	SSX4	"Synovial sarcoma, X breakpoint 4"	SSX4	6759	ENSG00000268009			Ssxb2 (MGI:2446771)			
chrX	48458536	48470255	Xp11.23	Xp11.23		300649	"SLC38A5, SN2"	"Solute carrier family 38 (amino acid transporter), member 5"	SLC38A5	92745	ENSG00000017483			Slc38a5 (MGI:2148066)			
chrX	48476020	48486363	Xp11.23	Xp11.23		300499	"FTSJ1, JM23, SPB1, MRX44, MRX9"	FTSJ homolog 1	FTSJ1	24140	ENSG00000068438		"Mental retardation, X-linked 9/44, 309549 (3), X-linked recessive"	Ftsj1 (MGI:1859648)			
chrX	48508958	48520813	Xp11.23	Xp11.23		300651	"PORCN, PORC, DHOF, FODH"	"Porcupine, Drosophila, homolog of"	PORCN	64840	ENSG00000102312		"Focal dermal hypoplasia, 305600 (3), X-linked dominant"	Porcn (MGI:1890212)			
chrX	48521775	48528715	Xp11.23-p11.22	Xp11.23		300205	"EBP, CDPX2, CPXD, CPX, MEND"	Emopamil-binding protein	EBP	10682	ENSG00000147155		"Chondrodysplasia punctata, X-linked dominant, 302960 (3), X-linked dominant; MEND syndrome, 300960 (3), X-linked recessive"	Ebp (MGI:107822)			
chrX	48539618	48562608	Xp11.3-p11.23	Xp11.23		311240	"TBC1D25, OATL1"	"TBC1 domain family, member 25"	TBC1D25	4943	ENSG00000068354			Tbc1d25 (MGI:2444862)			
chrX	48574352	48581164	Xp11.23	Xp11.23		300027	RBM3	RNA binding motif protein 3	RBM3	5935	ENSG00000102317			"Rbm3,Rbm3-ps (MGI:1099460,MGI:3642874)"			
chrX	48590052	48605193	Xp11.23	Xp11.23		300512	WDR13	WD repeat-containing protein 13	WDR13	64743	ENSG00000101940			Wdr13 (MGI:1914661)			
chrX	48683752	48691426	Xp11.23-p11.22	Xp11.23		300392	"WAS, IMD2, THC1, SCNX"	Wiskott-Aldrich syndrome gene	WAS	7454	ENSG00000015285	t(18;X)(q11.2;p11.2); distal to TIMP	"Neutropenia, severe congenital, X-linked, 300299 (3), X-linked recessive; Thrombocytopenia, X-linked, 313900 (3), X-linked recessive; Thrombocytopenia, X-linked, intermittent, 313900 (3), X-linked recessive; Wiskott-Aldrich syndrome, 301000 (3), X-linked recessive"	Was (MGI:105059)			
chrX	48695553	48709015	Xp11.23	Xp11.23		300254	SUV39H1	"Suppressor of variegation 3-9, Drosophila, homolog of, 1"	SUV39H1	6839	ENSG00000101945			Suv39h1 (MGI:1099440)			
chrX	48786539	48794310	Xp11.23	Xp11.23		305371	"GATA1, GF1, ERYF1, NFE1, XLTDA, XLTT, XLANP"	GATA-binding protein-1 (globin transcription factor-1)	GATA1	2623	ENSG00000102145		"Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835 (3), X-linked recessive; Leukemia, megakaryoblastic, with or without Down syndrome, somatic, 190685 (3); Thrombocytopenia with beta-thalassemia, X-linked, 314050 (3), X-linked recessive; Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367 (3), X-linked recessive"	Gata1 (MGI:95661)			
chrX	48801376	48824981	Xp11.23	Xp11.23		300272	"HDAC6, CPBHM"	Histone deacetylase 6	HDAC6	10013	ENSG00000094631	mutation identified in 1 CPBHM family	"?Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, 300863 (3), X-linked dominant"	Hdac6 (MGI:1333752)			
chrX	48826512	48829868	Xp11.2	Xp11.23		300437	"HRAS2, HRASP"	v-Ha-ras harvey rat sarcoma viral oncogene homolog 2	ERAS	3266	ENSG00000187682			Eras (MGI:2665023)			
chrX	48831091	48835637	Xp11.3	Xp11.23		300399	"PCSK1N, PROSAAS"	"Proprotein convertase, subtilisin/kexin-type, 1, inhibitor of"	PCSK1N	27344	ENSG00000102109			Pcsk1n (MGI:1353431)			
chrX	48893446	48898142	Xp11.2	Xp11.23		300249	"TIMM17B, TIM17B"	"Translocase of inner mitochondrial membrane 17, yeast, homolog of, B"	TIMM17B	10245	ENSG00000126768			Timm17b (MGI:1343176)			
chrX	48897861	48903144	Xp11.23	Xp11.23		300463	"PQBP1, NPW38, SHS, MRX55, MRXS3, RENS1, MRXS8"	Polyglutamine-binding protein 1	PQBP1	10084	ENSG00000102103		"Renpenning syndrome, 309500 (3), X-linked recessive"	Pqbp1 (MGI:1859638)			
chrX	48903179	48911957	Xp11.23-p11.22	Xp11.23		314375	"SLC35A2, UGALT, UGTL, UGT2, CDGX, CDG2M"	"Solute carrier family 35 (UDP-galactose transporter), member 2"	SLC35A2	7355	ENSG00000102100		"Congenital disorder of glycosylation, type IIm, 300896 (3), X-linked dominant, Somatic mosaicism"				
chrX	48913181	48919135	Chr.X	Xp11.23		300295	PIM2	Oncogene PIM2	PIM2	11040	ENSG00000102096			Pim2 (MGI:97587)			
chrX	48922023	48960782	Xp11.23	Xp11.23		300713	"OTUD5, DUBA"	OTU domain-containing protein 5	OTUD5	55593	ENSG00000068308						
chrX	48960982	48972102	Xp11.23	Xp11.23		300281	KCND1	"Potassium voltage-gated channel, SHAL-related subfamily, member 1"	KCND1	3750	ENSG00000102057			Kcnd1 (MGI:96671)			
chrX	48973719	49002263	Xp11.23	Xp11.23		300408	"GRIPAP1, GRASP1, KIAA1167"	GRIP1-associated protein 1	GRIPAP1	56850	ENSG00000068400			Gripap1 (MGI:1859616)			
chrX	49028725	49043516	Xp11.22	Xp11.23		314310	"TFE3, RCCX1"	Transcription factor for IgH enhancer	TFE3	7030	ENSG00000068323	fuses with PRCC in RCCP	"Renal cell carcinoma, papillary, 1, 300854 (3)"	Tfe3 (MGI:98511)			
chrX	49053431	49069857	Xp11.23	Xp11.23		300947	CCDC120	Coiled-coil domain-containing protein 120	CCDC120	90060	ENSG00000147144			Ccdc120 (MGI:1859619)			
chrX	49071155	49074044	Xp11.23	Xp11.23		300840	"PRAF2, JM4"	"PRA1 domain family, member 2"	PRAF2	11230	ENSG00000243279			Praf2 (MGI:1859607)			
chrX	49074432	49101120	Xp11.23	Xp11.23		300526	"WDR45, WIPI4, NBIA5"	WD repeat-containing protein 45	WDR45	11152	ENSG00000196998	?pseudogene on 4q31.3	"Neurodegeneration with brain iron accumulation 5, 300894 (3), X-linked dominant"	Wdr45 (MGI:1859606)			
chrX	49113384	49124546	Xp11.23	Xp11.23		301003	"GPKOW, GPATCH5"	G-patch domain and KO@ motifs	GPKOW	27238	ENSG00000068394			Gpkow (MGI:1859610)			
chrX	49171836	49175119	Xp11.23-p11.22	Xp11.23		300112	PLP2	Proteolipid protein 2	PLP2	5355	ENSG00000102007			Plp2 (MGI:1298382)			
chrX	49174801	49186399	Xp11.23	Xp11.23		300111	"PRICKLE3, LMO6"	"Prickle, Drosophila, homolog of, 3"	PRICKLE3	4007	ENSG00000012211			Prickle3 (MGI:1859635)			
chrX	49187811	49200201	Xp11.23-p11.22	Xp11.23		313475	"SYP, MRXSYP"	Synaptophysin	SYP	6855	ENSG00000102003		"Mental retardation, X-linked 96, 300802 (3), X-linked dominant"	Syp (MGI:98467)			
chrX	49205062	49233403	Xp11.23	Xp11.23		300110	"CACNA1F, CSNB2, CORDX3, CSNB2A, AIED, OA2"	"Calcium channel, voltage-dependent, alpha-1F subunit"	CACNA1F	778	ENSG00000102001		"Aland Island eye disease, 300600 (3), X-linked; Cone-rod dystrophy, X-linked, 3, 300476 (3), X-linked recessive; Night blindness, congenital stationary (incomplete), 2A, X-linked, 300071 (3), X-linked"	Cacna1f (MGI:1859639)			
chrX	49235466	49250525	Xp11.23	Xp11.23		300859	"CCDC22, RTSC2"	Coiled-coil domain-containing protein 22	CCDC22	28952	ENSG00000101997		"Ritscher-Schinzel syndrome 2, 300963 (3), X-linked recessive"	Ccdc22 (MGI:1859608)			
chrX	49250435	49264931	Xp11.23-q13.3	Xp11.23		300292	"FOXP3, IPEX, AIID, XPID, PIDX"	Forkhead box P3 (scurfin)	FOXP3	50943	ENSG00000049768		"{Diabetes mellitus, type I, susceptibility to}, 222100 (3), Autosomal recessive; Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 (3), X-linked recessive"	Foxp3 (MGI:1891436)			
chrX	49303645	49319843	Xp11.23	Xp11.23		300737	GAGE10	G antigen 10	GAGE10	102724473	ENSG00000215274						
chrX	49322029	49329386	Xp11.23	Xp11.23		300733	GAGE12J	G antigen 12J	GAGE12J	729396	ENSG00000224659						
chrX	49331602	49338951	Xp11.23	Xp11.23		300734	GAGE13	G antigen 13	GAGE13	645051	ENSG00000274274						
chrX	49532176	49539540	Xp11.23	Xp11.23		300727	GAGE12C	G antigen 12C	GAGE12C	729422	ENSG00000237671						
chrX	49541721	49549106	Xp11.23	Xp11.23		300728	GAGE12D	G antigen 12D	GAGE12D	100132399	ENSG00000227488						
chrX	49551288	49558648	Xp11.23	Xp11.23		300729	GAGE12E	G antigen 12E	GAGE12E	729431	ENSG00000216649						
chrX	49560807	49568207	Xp11.23	Xp11.23		300730	GAGE12F	G antigen 12F	GAGE12F	100008586	ENSG00000236362						
chrX	49570396	49577756	Xp11.23	Xp11.23		300731	GAGE12G	G antigen 12G	GAGE12G	645073	ENSG00000215269						
chrX	49579948	49587303	Xp11.23	Xp11.23		300732	GAGE12H	G antigen 12H	GAGE12H	729442	ENSG00000224902						
chrX	49589514	49596826	Xp11.23	Xp11.23		300720	GAGE2A	G antigen 2A	GAGE2A	729447	ENSG00000189064						
chrX	49598991	49608535	Xp11.23	Xp11.23		300594	GAGE1	G antigen 1	GAGE1	2543	ENSG00000205777						
chrX	49687449	49696018	Xp11.23	Xp11.23		300288	"GAGEB1, PAGE1"	"P antigen family, member 1"	PAGE1	8712	ENSG00000068985						
chrX	49829259	49834263	Xp11.23	Xp11.23		300287	"PAGE4, GAGEC1"	"P antigen family, member 4"	PAGE4	9506	ENSG00000101951						
chrX	49879866	49882564	Xp11.2	Xp11.23		300975	"USP27X, USP22L, MRX105"	"Ubiquitin-specific protease 27, X-linked"	USP27X	389856	ENSG00000273820		"Mental retardation 105, 300984 (3), X-linked recessive"	Usp27x (MGI:1859645)			
chrX	49922614	50099234	Xp11.22	Xp11.23		300008	"CLCN5, CLCK2, NPHL2, DENTS, NPHL1"	Chloride channel-5	CLCN5	1184	ENSG00000171365		"Dent disease, 300009 (3), X-linked recessive; Hypophosphatemic rickets, 300554 (3), X-linked recessive; Nephrolithiasis, type I, 310468 (3), X-linked recessive; Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis, 308990 (3), X-linked recessive"	Clcn5 (MGI:99486)			
chrX	50014597	50014682	Xp11.23	Xp11.23		300893	MIR502	Micro RNA 502	MIR502	574504							
chrX	50100000	54800000	Xp11.22			300705	"DUPXp11.22, MRX17, MRX31"	Xp11.22 microduplication syndrome				minimal duplicated region 228 kb overlapping HUWE1 and HSD17B10	"Xp11.22 microduplication syndrome, 300705 (4)"				
chrX	50100000	54800000	Xp11.22			300704	HPCX2	"Prostate cancer, hereditary, X-linked 2"		100188769		associated with rs5945572	"{Prostate cancer, hereditary, X-linked 2}, 300704 (2)"				
chrX	50100000	54800000	Xp11.22			300856	HYSP4	"Hypospadias 4, X-linked, susceptibility to"		100689214		associated with rs1934179 and rs7063116	"{Hypospadias 4, X-linked, susceptibility to}, 300856 (2)"				
chrX	50190767	50201012	Xp11.2	Xp11.22		300185	"AKAP4, AKAP82, HI, FSC1"	"A-kinase anchor protein 4, 82kD"	AKAP4	8852	ENSG00000147081			Akap4 (MGI:102794)			
chrX	50202712	50351913	Xp11.22	Xp11.22		300456	CCNB3	Cyclin B3	CCNB3	85417	ENSG00000147082			Ccnb3 (MGI:2183443)			
chrX	50365406	50470850	Xp11.22	Xp11.22		300837	DGKK	"Diacylglycerol kinase, kappa, 142kD"	DGKK	139189	ENSG00000274588			Dgkk (MGI:3580254)			
chrX	50575533	50814163	Xp11.2	Xp11.22		300579	"SHROOM4, KIAA1202, SDSX"	Shroom family member 4	SHROOM4	57477	ENSG00000158352		"Stocco dos Santos X-linked mental retardation syndrome, 300434 (3), X-linked"	Shroom4 (MGI:2685570)			
chrX	50910734	50916640	Xp11.2	Xp11.22		300247	"BMP15, GDF9B, ODG2, POF4"	Bone morphogenetic protein 15	BMP15	9210	ENSG00000130385		"Ovarian dysgenesis 2, 300510 (3), X-linked; Premature ovarian failure 4, 300510 (3), X-linked"	Bmp15 (MGI:1316745)			
chrX	51332230	51337524	Xp11.23	Xp11.22		300527	"NUDT10, DIPP3A, APS2"	Nucleoside diphosphate-linked moiety X motif 10	NUDT10	170685	ENSG00000122824						
chrX	51490010	51496606	Xp11.23	Xp11.22		300528	"NUDT11, DIPP3B, APS1"	Nucleoside diphosphate-linked moiety X motif 11	NUDT11	55190	ENSG00000196368			"Nudt11,Nudt10 (MGI:2147931,MGI:1930957)"			
chrX	51743384	51746231	Xp11.23-p11.21	Xp11.22		300418	"GSPT2, GST2, ERF3B"	G1- to S-phase transition 2	GSPT2	23708	ENSG00000189369			Gspt2 (MGI:1316727)			
chrX	51802997	51902353	Xp11.23	Xp11.22		300224	MAGED1	"Melanoma antigen, family D, 1"	MAGED1	9500	ENSG00000179222			Maged1 (MGI:1930187)			
chrX	52061826	52069271	Xp11	Xp11.22		300765	MAGED4B	"Melanoma antigen, family D, 4B"	MAGED4B	81557	ENSG00000187243						
chrX	52184822	52192267	Xp11	Xp11.22		300702	"MAGED4, MAGEE1, KIAA1859"	"Melanoma antigen, family D, 4"	MAGED4	728239	ENSG00000154545						
chrX	52368995	52375682	Xp11.22	Xp11.22		300416	"XAGE2, GAGED3"	"X antigen family, member 2"	XAGE2	9502	ENSG00000155622						
chrX	52495667	52500814	Xp11.22	Xp11.22		300742	XAGE1A	"X antigen family, member 1A"	XAGE1A	653220	ENSG00000204379						
chrX	52495667	52500814	Xp11.22	Xp11.22		300743	XAGE1B	"X antigen family, member 1B"	XAGE1A	653220	ENSG00000204379						
chrX	52512073	52517220	Xp11.22	Xp11.22		300744	XAGE1C	"X antigen family, member 1C"	XAGE1B	653067	ENSG00000204382						
chrX	52512073	52517220	Xp11.22	Xp11.22		300745	XAGE1E	"X antigen family, member 1E"	XAGE1B	653067	ENSG00000204382						
chrX	52512073	52517220	Chr.X	Xp11.22		300289	"GAGED2, XAGE1"	"G antigen, family D, 2"	XAGE1B	653067	ENSG00000204382						
chrX	52622934	52633947	Xp11.22	Xp11.22		300543	SSX8	"Sarcoma, synovial, X breakpoint 8"	SSX8	280659							
chrX	52644060	52654899	Xp11.22	Xp11.22		300542	SSX7	"Sarcoma, synovial, X breakpoint 7"	SSX7	280658	ENSG00000187754						
chrX	52696895	52707226	Xp11.22	Xp11.22		300192	SSX2	"Sarcoma, synovial, X breakpoint 2"	SSX2	6757	ENSG00000241476		"?Sarcoma, synovial, 300813 (3)"				
chrX	52796145	52797347	Xp11	Xp11.22		300668	SPANXN5	"SPANX family, member N5"	SPANXN5	494197	ENSG00000204363						
chrX	52862527	52868139	Xp11.22	Xp11.22		300740	"XAGE3, PLAC6"	"X antigen family, member 3"	XAGE3	170626	ENSG00000171402						
chrX	53049323	53080614	Xp11.22	Xp11.22		300253	"GPR173, SREB3"	G protein-coupled receptor 173	GPR173	54328	ENSG00000184194			Gpr173 (MGI:1918021)			
chrX	53082359	53088545	Xp11.2	Xp11.22		300564	"TSPYL2, CDA1, DENTT, CINAP"	TSPY-like 2	TSPYL2	64061	ENSG00000184205			Tspyl2 (MGI:106244)			
chrX	53159734	53225421	Xp11.22-p11.21	Xp11.22		314690	"KDM5C, JARID1C, SMCX, DXS1272E, XE169, MRXSCJ"	"Lysine-specific demethylase 5C (Jumonji, AT-rich interactive domain 1C)"	KDM5C	8242	ENSG00000126012	escapes inactivation	"Mental retardation, X-linked, syndromic, Claes-Jensen type, 300534 (3), X-linked recessive"	Kdm5c (MGI:99781)			
chrX	53225783	53321355	Xp11.22	Xp11.22		300522	"IQSEC2, KIAA0522, MRX1, MRX78"	IQ motif- and Sec7 domain-containing protein 2	IQSEC2	23096	ENSG00000124313		"Mental retardation, X-linked 1/78, 309530 (3), X-linked dominant"	Iqsec2 (MGI:3528396)			
chrX	53374148	53422727	Xp11.22-p11.21	Xp11.22		300040	"SMC1A, SMC1L1, SMC1, DXS423E, KIAA0178, CDLS2"	"Segregation of mitotic chromosomes 1 (SMC1, yeast, homolog of; DXS423E; SB1.8)"	SMC1A	8243	ENSG00000072501	escapes lyonization	"Cornelia de Lange syndrome 2, 300590 (3), X-linked dominant"	Smc1a (MGI:1344345)			
chrX	53431257	53434375	Xp11.2	Xp11.22		300256	"HSD17B10, HADH2, ERAB, MRXS10, HSD10MD"	17-beta-hydroxysteroid dehydrogenase X	HSD17B10	3028	ENSG00000072506		"HSD10 mitochondrial disease, 300438 (3), X-linked dominant"	Hsd17b10 (MGI:1333871)			
chrX	53532095	53686728	Xp11.2	Xp11.22		300697	"HUWE1, UREB1, KIAA0312, LASU1"	"HECT, UBA, and WWE domains-containing protein 1"	HUWE1	10075	ENSG00000086758		"Mental retardation, X-linked syndromic, Turner type, 300706 (3)"	Huwe1 (MGI:1926884)			
chrX	53556222	53556340	Xp11.22	Xp11.22		300810	"MIR98, MIRN98"	Micro RNA 98	MIR98	407054							
chrX	53557191	53557273	Xp11.22	Xp11.22		300721	"MIRLET7F2, LET7F2, MIRNLET7F2"	Micro RNA Let7f2	MIRLET7F2	406889							
chrX	53936679	54048934	Xp11.2	Xp11.22		300560	"PHF8, ZNF422, KIAA1111, MRXSSD"	PHD finger protein 8	PHF8	23133	ENSG00000172943		"Mental retardation syndrome, X-linked, Siderius type, 300263 (3), X-linked recessive"	Phf8 (MGI:2444341)			
chrX	54068323	54183283	Xp11.2	Xp11.22		300741	"FAM120C, CXorf17"	"Family with sequence similarity 120, member C"	FAM120C	54954	ENSG00000184083			Fam120c (MGI:2387687)			
chrX	54192822	54358694	Xp11.2	Xp11.22		300358	"WNK3, PRKWNK3, KIAA1566"	WNK lysine deficient protein kinase 3	WNK3	65267	ENSG00000196632			Wnk3 (MGI:2652875)			
chrX	54440374	54448031	Xp11.22	Xp11.22		300945	"TSR2, WGG1, DBA14"	"TSR2, 20S rRNA accumulation, S. cerevisiae, homolog of"	TSR2	90121	ENSG00000158526	mutation identified in 1 DBA14 family	"?Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, 300946 (3), X-linked recessive"	Tsr2 (MGI:1916749)			
chrX	54445453	54496165	Xp11.21	Xp11.22		300546	"FGD1, FGDY, AAS, MRXS16"	"FYVE, RhoGEF, and PH domain-containing protein 1"	FGD1	2245	ENSG00000102302		"Aarskog-Scott syndrome, 305400 (3), X-linked recessive; Mental retardation, X-linked syndromic 16, 305400 (3), X-linked recessive"	Fgd1 (MGI:104566)			
chrX	54530210	54567286	Xp11.22	Xp11.22		300873	GNL3L	Guanine nucleotide binding protein-like 3-like protein	GNL3L	54552	ENSG00000130119			Gnl3l (MGI:2448557)			
chrX	54800000	109400000	Xp11.21-q22.3			300504	MRX52	"Mental retardation, X-linked 52"	ATRX	546	ENSG00000085224	max lod at DXS559	"Mental retardation, X-linked 52, 300504 (2), X-linked recessive"				
chrX	54807598	54816014	Xp11.2	Xp11.21		300470	"MAGED2, MAGED, BARTS5"	"Melanoma antigen, family D, 2"	MAGED2	10916	ENSG00000102316		"Bartter syndrome, type 5, antenatal, transient, 300971 (3), X-linked recessive"	Maged2 (MGI:1933391)			
chrX	54814369	54814499	Xp11.21	Xp11.21		300662	SNORA11	"Small nucleolar RNA, H/ACA box, 11"	SNORA11	677799		in intron 1 of MAGED2					
chrX	54920562	54931435	Xp11.22-p11.21	Xp11.21		300132	TRO	Trophinin	TRO	7216	ENSG00000067445			Tro (MGI:1928994)			
chrX	54933133	55000051	Xp11.21	Xp11.21		311790	"PFKFB1, PFRX"	"Fructose-2,6-bisphosphatase"	PFKFB1	5207	ENSG00000158571	?Xq27-q25; ?Xcen-q13		Pfkfb1 (MGI:107816)			
chrX	55000322	55007872	Xp11.21	Xp11.21		300773	"APEX2, APE2, XTH2, APEXL2"	APEX nuclease (apurinic/apyrimidinic endonuclease) 2	APEX2	27301	ENSG00000169188			Apex2 (MGI:1924872)			
chrX	55009054	55031063	Xp11.21	Xp11.21		301300	"ALAS2, ANH1, ASB, XLEPP, XLSA, SIDBA1"	"Aminolevulinate, delta-, synthase-2"	ALAS2	212	ENSG00000158578		"Anemia, sideroblastic, 1, 300751 (3), X-linked recessive; Protoporphyria, erythropoietic, X-linked, 300752 (3), X-linked dominant"	Alas2 (MGI:87990)			
chrX	55089051	55092835	Xp11.21	Xp11.21		300738	"PAGE2, GAGEC2"	"P antigen family, member 2"	PAGE2	203569	ENSG00000234068						
chrX	55220346	55224107	Xp11.21	Xp11.21		301009	"PAGE5, CT16, GAGEE1"	"P antigen family, member 5"	PAGE5	90737	ENSG00000158639						
chrX	55257600	55264915	Xp11.21	Xp11.21		300739	"PAGE3, GAGEC1"	"P antigen family, member 3"	PAGE3	139793	ENSG00000204279						
chrX	55452088	55453567	Xp11.21	Xp11.21		300548	"MAGEH1, MAGEH"	"Melanoma antigen, family H, 1"	MAGEH1	28986	ENSG00000187601			Mageh1 (MGI:1922875)			
chrX	55623399	55626187	Xp11.21	Xp11.21		300949	"FOXR2, FOXN6"	Forkhead box R2	FOXR2	139628	ENSG00000189299			Foxr2 (MGI:3511682)			
chrX	55717676	55760208	Xp11.21	Xp11.21		300725	"RRAGB, RAGB"	Ras-related GTP-binding protein B	RRAGB	10325	ENSG00000083750			Rragb (MGI:3038613)			
chrX	55908122	56291530	Chr.X	Xp11.21		300286	"KLF8, ZNF741, BKLF3"	Kruppel-like factor 8	KLF8	11279	ENSG00000102349			Klf8 (MGI:2442430)			
chrX	56563592	56567009	Xp11.23-p11.1	Xp11.21		300264	"UBQLN2, PLIC2, CHAP1, ALS15"	Ubiquilin 2	UBQLN2	29978	ENSG00000188021		"Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, 300857 (3), X-linked dominant"	Ubqln2 (MGI:1860283)			
chrX	56729218	56819178	Xp11.1	Xp11.21		300992	"NBDY, LINC01420, NOBODY"	Negative regulator of P-body association	NBDY	550643	ENSG00000204272						
chrX	57112141	57121904	Xp11.21	Xp11.21		300517	SPIN2	"Spindlin family, member 2"	SPIN2B	474343	ENSG00000186787			"Gm21637,Spin2e,Spin2d,Gm5923,Gm3757,Gm5926,Gm2854,Spin2-ps4,Gm2892,Spin2-ps1,Gm21466,Spin2-ps3,Spin2-ps2 (MGI:1922101,MGI:3781932,MGI:3645924,MGI:3650966,MGI:3645574,MGI:5434847,MGI:5434821,MGI:3781070,MGI:3647272,MGI:3781026,MGI:3805546,MGI:5434992,MGI:3705652)"			
chrX	57121860	57489195	Xp11	Xp11.21		300654	FAAH2	Fatty acid amide hydrolase 2	FAAH2	158584	ENSG00000165591						
chrX	57133042	57138687	Xp11.21	Xp11.21		300621	DSF34	DXF34 gene	SPIN2A	54466	ENSG00000147059			"Gm21637,Spin2e,Spin2d,Gm5923,Gm3757,Gm5926,Gm2854,Spin2-ps4,Gm2892,Spin2-ps1,Gm21466,Spin2-ps3,Spin2-ps2 (MGI:1922101,MGI:3781932,MGI:3645924,MGI:3650966,MGI:3645574,MGI:5434847,MGI:5434821,MGI:3781070,MGI:3647272,MGI:3781026,MGI:3805546,MGI:5434992,MGI:3705652)"			
chrX	57591835	57597476	Xp11.21	Xp11.21		300236	ZXDB	"Zinc finger-encoding gene, X-linked, duplicated, B"	ZXDB	158586	ENSG00000198455			Zxdb (MGI:3694898)			
chrX	57905429	57910632	Xp11.21	Xp11.21		300235	ZXDA	"Zinc finger-encoding gene, X-linked, duplicated, A"	ZXDA	7789	ENSG00000198205						
chrX	61000000	68500000	Xq11-q12			300710	AGA2	"Alopecia, androgenetic, 2"		100188771		associated with rs6152	"Alopecia, androgenetic, 2, 300710 (2)"				
chrX	61000000	156040895	Xq			300082	CGF1	"Cognitive function-1, social"	CGF1	1083		imprinted locus	"[Social cognition], 300082 (2), X-linked"				
chrX	61000000	156040895	Xq			300010	"DXS435E, A11"	A-11 gene		8248							
chrX	61000000	156040895	Xq			300125	MGR2	"Migraine, familial typical, susceptibility to, 2"		8249			"{Migraine, familial typical, susceptibility to, 2}, 300125 (2), X-linked"				
chrX	61000000	156040895	Xq			300259	MTBSX	"Mycobacterium tuberculosis, susceptibility to, X-linked"		57789			"{Mycobacterium tuberculosis, susceptibility, X-linked}, 300259 (2)"				
chrX	63634966	63785545	Xq22.1	Xq11.1		300429	"ARHGEF9, PEM2, KIAA0424, EIEE8"	Rho guanine nucleotide exchange factor 9	ARHGEF9	23229	ENSG00000131089		"Epileptic encephalopathy, early infantile, 8, 300607 (3), X-linked recessive"	Arhgef9 (MGI:2442233)			
chrX	63800000	65400000	Xq11.2			300266	SPG16	"Spastic paraplegia 16, X-linked, complicated"	SPG16	57760			"Spastic paraplegia 16, X-linked, complicated, 300266 (2), X-linked recessive"				
chrX	64185116	64205743	Xq11.1	Xq11.2		300647	"AMER1, FAM123B, WTX, OSCS"	APC membrane recruitment protein 1	AMER1	139285	ENSG00000184675		"Osteopathia striata with cranial sclerosis, 300373 (3), X-linked dominant"	Amer1 (MGI:1919595)			
chrX	64224191	64230630	Xq11.2	Xq11.2		300891	ASB12	Ankyrin repeat- and SOCS box-containing protein 12	ASB12	142689	ENSG00000198881			Asb12 (MGI:1917642)			
chrX	64915801	65034743	Xq11.2	Xq11.2		300897	"ZC4H2, KIAA1166, WRWF"	Zinc finger C4H2 domain-containing protein	ZC4H2	55906	ENSG00000126970		"Wieacker-Wolff syndrome, 314580 (3), X-linked recessive"	Zc4h2 (MGI:2679294)			
chrX	65034814	65507886	Xq12	Xq11-q12		300889	"ZC3H12B, MCPIP2"	Zinc finger CCCH domain-containing protein 12B	ZC3H12B	340554	ENSG00000102053			Zc3h12b (MGI:2442133)			
chrX	65400000	99100000	Xq12-q21.3			300454	MRX77	"Mental retardation, X-linked 77"	MRX77	93991			"Mental retardation, X-linked 77, 300454 (2), X-linked recessive"				
chrX	65400000	92700000	Xq12-q21.31			300709	MRXS9	"Mental retardation, X-linked, syndromic 9"				between DXS1111 and DXS1197	"Mental retardation, X-linked, syndromic 9, 300709 (2)"				
chrX	65512581	65534805	Xq12	Xq12		300964	"LAS1L, WTS"	Las1-like ribosome biogenesis factor	LAS1L	81887	ENSG00000001497		"Wilson-Turner syndrome, 309585 (3), X-linked recessive"	Las1l (MGI:1923380)			
chrX	65588381	65741930	Xq11.2-q12	Xq12		309845	"MSN, IMD50"	Moesin	MSN	4478	ENSG00000147065		"Immunodeficiency 50, 300988 (3), X-linked recessive"	Msn (MGI:97167)			
chrX	66018869	66018978	Xq12	Xq12		300694	"MIR223, MIRN223"	Micro RNA 223	MIR223	407008							
chrX	66021737	66040124	Xq12	Xq12		300353	Z39IG	Immunoglobulin superfamily protein Z39IG	VSIG4	11326	ENSG00000155659			Vsig4 (MGI:2679720)			
chrX	66162525	66267388	Xq11-q12	Xq12		300167	HEPH	Hephaestin	HEPH	9843	ENSG00000089472			Heph (MGI:1332240)			
chrX	66594383	66639302	Xq12	Xq12		300276	"EDAR2, XEDAR, EDAA2R"	Ectodysplasin A2 receptor	EDA2R	60401	ENSG00000131080			Eda2r (MGI:2442860)			
chrX	67544622	67730618	Xq11-q12	Xq12		313700	"AR, DHTR, TFM, SBMA, KD, SMAX1, HYSP1"	Androgen receptor (dihydrotestosterone receptor)	AR	367	ENSG00000169083		"Androgen insensitivity, 300068 (3), X-linked recessive; Androgen insensitivity, partial, with or without breast cancer, 312300 (3), X-linked recessive; Hypospadias 1, X-linked, 300633 (3), X-linked recessive; {Prostate cancer, susceptibility to}, 176807 (3), Autosomal dominant; Spinal and bulbar muscular atrophy of Kennedy, 313200 (3), X-linked recessive"	Ar (MGI:88064)			
chrX	68042343	68433840	Xq12	Xq12		300127	"OPHN1, MRX60"	Oligophrenin-1	OPHN1	4983	ENSG00000079482		"Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 (3), X-linked recessive"	Ophn1 (MGI:2151070)			
chrX	68498361	68572458	Xq12-q13.1	Xq12-q13		300996	YIPF6	"YIP1 domain family, member 6"	YIPF6	286451	ENSG00000181704			Yipf6 (MGI:1925179)			
chrX	68500000	103300000	Xq13.1-q22.1			300580	CFTDX	"Myopathy, congenital, with fiber-type disproportion, X-linked"		100188765		between DXS8019 and DXS99	"Myopathy, congenital, with fiber-type disproportion, X-linked, 300580 (2), X-linked dominant"				
chrX	68500000	109400000	Xq13-q22			309605	"MCS, MRXS4"	"Miles-Carpenter syndrome (mental retardation, X-linked, syndromic 4, with congenital contractures and low fingertip arches)"				linked to DXYS1	"Miles-Carpenter syndrome, 309605 (2)"				
chrX	68647668	68725841	Xq13.1	Xq13.1		300689	"STARD8, DLC3, STARTGAP3, KIAA0189"	START domain-containing protein 8	STARD8	9754	ENSG00000130052			Stard8 (MGI:2448556)			
chrX	68828996	68842163	Xq12	Xq13.1		300035	"EFNB1, EPLG2, CFNS, CFND"	eph-related receptor tyrosine kinase ligand 2 (ephrin B1)	EFNB1	1947	ENSG00000090776	?CFNS also on Xp22	"Craniofrontonasal dysplasia, 304110 (3), X-linked dominant"	Efnb1 (MGI:102708)			
chrX	69160737	69165521	Xq13.1	Xq13.1		300420	PJA1	Praja 1	PJA1	64219	ENSG00000181191			Pja1 (MGI:1101765)			
chrX	69616066	70039471	Xq12-q13.1	Xq13.1		300451	"EDA, ED1, ECTD1, HED1, STHAGX1"	Ectodysplasin A	EDA	1896	ENSG00000158813		"Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3), X-linked recessive; Tooth agenesis, selective, X-linked 1, 313500 (3), X-linked dominant"				
chrX	70040541	70049969	Xq13.1	Xq13.1		300925	"AWAT2, DC4, MFAT"	Acyl-CoA wax alcohol acyltransferase 2	AWAT2	158835	ENSG00000147160			Awat2 (MGI:3045345)			
chrX	70062490	70064178	Xq13.1	Xq13.1		300714	"OTUD6A, DUBA2"	OTU domain-containing protein 6A	OTUD6A	139562	ENSG00000189401			Otud6a (MGI:3644685)			
chrX	70133448	70166323	Xq13.1-q13.3	Xq13.1		300139	IGBP1	Immunoglobulin-binding protein 1	IGBP1	3476	ENSG00000089289		"Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia, 300472 (3), X-linked recessive"	Igbp1 (MGI:1346500)			
chrX	70177482	70205702	Xq13.1	Xq13.1		300926	"DGAT2L6, DC3"	Diacylglycerol O-acyltransferase 2-like 6	DGAT2L6	347516	ENSG00000184210			Dgat2l6 (MGI:3045268)			
chrX	70233488	70240660	Xq13.1	Xq13.1		300924	"AWAT1, DGA2"	Acyl-CoA wax alcohol acyltransferase 1	AWAT1	158833	ENSG00000204195			Awat1 (MGI:3588200)			
chrX	70258165	70259803	Xq13	Xq13.1		300038	"P2RY4, NRU, P2Y4"	"Pyrimidinergic receptor P2Y, G-protein coupled, 4"	P2RY4	5030	ENSG00000186912			P2ry4 (MGI:1926594)			
chrX	70268334	70281839	Xcen-q21	Xq13.1		301770	"ARR3, MYP26"	"Arrestin 3, retinal"	ARR3	407	ENSG00000120500		"Myopia 26, X-linked, female-limited, 301010 (3), X-linked"	Arr3 (MGI:2159617)			
chrX	70286360	70289957	Xq13.1	Xq13.1		300632	"PDZD11, AIPP1, PISP"	PDZ domain-containing 11	PDZD11	51248	ENSG00000120509			Pdzd11 (MGI:1919871)			
chrX	70290028	70420923	Xq13.1	Xq13.1		300521	"KIF4A, KIF4, MRX100"	Kinesin family member 4A	KIF4A	24137	ENSG00000090889	mutation identified in 1 MRX100 family	"?Mental retardation, X-linked 100, 300923 (3), X-linked recessive"	Kif4 (MGI:108389)			
chrX	70423030	70433390	Xq13.1	Xq13.1		300940	"GDPD2, GDE3"	Glycerophosphodiester phosphodiesterase domain-containing protein 2	GDPD2	54857	ENSG00000130055			Gdpd2 (MGI:1918834)			
chrX	70444849	70505489	Xq13.1	Xq13.1		300189	"DLG3, NEDLG, SAP102, MRX90"	"Discs large, Drosophila, homolog of, 3"	DLG3	1741	ENSG00000082458		"Mental retardation, X-linked 90, 300850 (3), X-linked recessive"	Dlg3 (MGI:1888986)			
chrX	70511226	70908716	Xq13.1	Xq13.1		300311	"TEX11, SPGFX2"	Testis-expressed gene 11	TEX11	56159	ENSG00000120498		"Spermatogenic failure, X-linked, 2, 309120 (3), X-linked recessive"	Tex11 (MGI:1933237)			
chrX	70925578	70931124	Xq13.1	Xq13.1		300443	"SLC7A3, CAT3"	"Solute carrier family 7 (cationic amino acid transporter, y+ system), member 3"	SLC7A3	84889	ENSG00000165349			Slc7a3 (MGI:1100521)			
chrX	71059246	71073425	Xq13.1	Xq13.1		300883	SNX12	Sorting nexin 12	SNX12	29934	ENSG00000147164			Snx12 (MGI:1919331)			
chrX	71096148	71103533	Xq13.1	Xq13.1		300033	"FOXO4, MLLT7, AFX1"	Forkhead box O4	FOXO4	4303	ENSG00000184481			Foxo4 (MGI:1891915)			
chrX	71107403	71111630	Xq13	Xq13.1		308380	"IL2RG, SCIDX1, SCIDX, IMD4"	"Interleukin-2 receptor, gamma"	IL2RG	3561	ENSG00000147168	linked to DXS159	"Combined immunodeficiency, X-linked, moderate, 312863 (3), X-linked recessive; Severe combined immunodeficiency, X-linked, 300400 (3), X-linked recessive"	Il2rg (MGI:96551)			
chrX	71118555	71142453	Xq13	Xq13.1		300188	"MED12, TNRC11, TRAP230, HOPA, KIAA0192, OKS, FGS1, OHDOX"	"Mediator of RNA polymerase II transcription, subunit 12, S. cerevisiae, homolog of"	MED12	9968	ENSG00000184634		"Lujan-Fryns syndrome, 309520 (3), X-linked recessive; Ohdo syndrome, X-linked, 300895 (3), X-linked recessive; Opitz-Kaveggia syndrome, 305450 (3), X-linked recessive"	Med12 (MGI:1926212)			
chrX	71144388	71175306	Xq13	Xq13.1		300336	"NLGN3, ASPGX1, AUTSX1"	Neuroligin 3	NLGN3	54413	ENSG00000196338		"{Asperger syndrome susceptibility, X-linked 1}, 300494 (3), Isolated cases, X-linked, Multifactorial; {Autism susceptibility, X-linked 1}, 300425 (3), Isolated cases, X-linked, Multifactorial"	Nlgn3 (MGI:2444609)			
chrX	71215211	71225214	Xq13.1	Xq13.1		304040	"GJB1, CX32, CMTX1"	"Gap junction protein, beta-1, 32kD (connexin 32)"	GJB1	2705	ENSG00000169562		"Charcot-Marie-Tooth neuropathy, X-linked dominant, 1, 302800 (3), X-linked dominant"	Gjb1 (MGI:95719)			
chrX	71239623	71255196	Xq13.1	Xq13.1		300061	"ZMYM3, ZNF261, DXS6673E"	"Zinc finger, MYM-type 3"	ZMYM3	9203	ENSG00000147130			Zmym3 (MGI:1927231)			
chrX	71283191	71301167	Xq13.1	Xq13.1		300084	"NONO, NRB54, MRXS34"	"Non-Pou domain-containing octamer (ATGCAAAT) binding protein (nuclear RNA-binding protein, 54-kD)"	NONO	4841	ENSG00000147140	2Mb proximal to PHKA1	"Mental retardation, X-linked, syndromic 34, 300967 (3), X-linked"	Nono (MGI:1855692)			
chrX	71301733	71305370	Xq12-q13	Xq13.1		300332	ITGB1BP2	"Integrin, beta-1, binding protein of, 2"	ITGB1BP2	26548	ENSG00000147166			Itgb1bp2 (MGI:1353420)			
chrX	71366219	71530524	Xq13	Xq13.1		313650	"TAF1, TAF2A, CCG1, BA2R, DYT3, MRXS33"	"TAF1 RNA polymerase II, TATA box-binding protein-associated factor, 250kD"	TAF1	6872	ENSG00000147133	SVA retrotransposon insertion	"Dystonia-Parkinsonism, X-linked, 314250 (3), X-linked recessive; Mental retardation, X-linked, syndromic 33, 300966 (3), X-linked recessive"	Taf1 (MGI:1336878)			
chrX	71491680	71492448	Xq12	Xq13.1		300452	"INGX, ING2"	"Inhibitor of growth, X-linked"	INGX	27160							
chrX	71533061	71575896	Xq13	Xq13.1		300255	"OGT, MRX106"	O-linked N-acetylglucosamine transferase	OGT	8473	ENSG00000147162		"Mental retardation, X-linked 106, 300997 (3), X-linked recessive"	Ogt (MGI:1339639)			
chrX	71578023	71613582	Xq13.1	Xq13.1		300369	ACRC	Acidic repeat-containing gene	GCNA	93953	ENSG00000147174						
chrX	71615912	71618516	Xq13	Xq13.1		300574	"CXCR3, GPR9, CD182"	"Chemokine, C-X-C motif, receptor 3 (G protein-coupled receptor-9)"	CXCR3	2833	ENSG00000186810	previously assigned to chr.8		Cxcr3 (MGI:1277207)			
chrX	72181675	72263963	Xq13	Xq13.1		300252	"PIN4, PAR14, EPVH"	"Peptidyl-prolyl cis/trans isomerase, nima-interacting, 4"	PIN4	5303	ENSG00000102309			Pin4 (MGI:1916963)			
chrX	72204654	72239046	Xq13.1	Xq13.1		300687	"ERCC6L, PICH"	ERCC6-like	ERCC6L	54821	ENSG00000186871			Ercc6l (MGI:2654144)			
chrX	72272602	72277290	Xq13.1	Xq13.1		312760	"RPS4X, CCG2, SCAR"	"Ribosomal protein S4, X-linked"	RPS4X	6191	ENSG00000198034	cen-RPS4X-PHKA1-XIST-qter in 2.6Mb					
chrX	72301637	72307186	Xq13.1	Xq13.1		300149	MSG1	Melanocyte-specific gene 1	CITED1	4435	ENSG00000125931			Cited1 (MGI:108023)			
chrX	72329515	72573102	Xq13	Xq13.1		300269	"HDAC8, MRXS6, CDLS5"	Histone deacetylase 8	HDAC8	55869	ENSG00000147099		"Cornelia de Lange syndrome 5, 300882 (3), X-linked dominant"	Hdac8 (MGI:1917565)			
chrX	72578813	72714180	Xq13	Xq13.1		311870	PHKA1	"Phosphorylase kinase, muscle, alpha polypeptide"	PHKA1	5255	ENSG00000067177	?proximal and close to PGKA;	"Muscle glycogenosis, 300559 (3), X-linked recessive"	Phka1 (MGI:97576)			
chrX	72872024	72943930	Xq13	Xq13.1		300878	DMRTC1	Doublesex- and MAB3-related transcription factor C1	DMRTC1	63947	ENSG00000269502						
chrX	73000000	74700000	Xq13.2			300262	MRXSAB	Abidi X-linked mental retardation syndrome		57792			"Mental retardation, X-linked syndromic, Abidi type, 300262 (2)"				
chrX	73212298	73214873	Xq13.2	Xq13.2		300026	"NAP1L2, BPX"	Nucleosome assembly protein 1-like 2	NAP1L2	4674	ENSG00000186462			Nap1l2 (MGI:106654)			
chrX	73447253	73454584	Xq13.2	Xq13.2		300025	CDX4	Caudal type homeo box transcription factor 4	CDX4	1046	ENSG00000131264			Cdx4 (MGI:88362)			
chrX	73563044	73687108	Xq13.2	Xq13.2		300922	"CHIC1, BRX"	Cystein-rich hydrophobic domain protein 1	CHIC1	53344	ENSG00000204116			Chic1 (MGI:1344694)			
chrX	73792204	73829230	Xq13.2	Xq13.2		300181	TSIX	X-inactivation-specific transcript-antisense	TSIX	9383							
chrX	73820650	73852752	Xq13.2	Xq13.2		314670	"XIC, XCE, XIST, SXI1"	X chromosome controlling element (X-inactivation center)	XIST	7503		"q13-q21; metaphase bend, or fold, at q13.3-q21.1"	"X-inactivation, familial skewed, 300087 (3)"				
chrX	73944323	74070383	Xq13.2	Xq13.2		300832	"NCRNA00183, JPX, ENOX"	Noncoding RNA 183	JPX	554203							
chrX	74028135	74293573	Xq13.2	Xq13.2		300936	"FTX, LINC00182"	"FTX transcript, XIST regulator, noncoding"	FTX	100302692							
chrX	74421492	74533928	Xq13.2	Xq13.2		300095	"SLC16A2, DXS128, XPCT"	"Solute carrier family 16 (monocarboxylic acid transporters), member 2"	SLC16A2	6567	ENSG00000147100		"Allan-Herndon-Dudley syndrome, 300523 (3), X-linked"	Slc16a2 (MGI:1203732)			
chrX	74582975	74614625	Xq13-q21	Xq13.2		300379	"RNF12, RLIM, MRX61"	Putative RING zinc finger protein NY-REN-43 antigen	RLIM	51132	ENSG00000131263		"Mental retardation, X-linked 61, 300978 (3), X-linked recessive"	Rlim (MGI:1342291)			
chrX	74732855	74925451	Xq13.2	Xq13.3		300524	"NEXMIF, KIAA2022, MRX98"	Neurite extension and migration factor	NEXMIF	340533	ENSG00000050030	inv(X)(q13;p22)	"Mental retardation, X-linked 98, 300912 (3), X-linked dominant"	Nexmif (MGI:2148050)			
chrX	75053279	75156339	Xq13.1-q13.3	Xq13.3		300135	"ABCB7, ABC7, ASAT"	ATP-binding cassette-7	ABCB7	22	ENSG00000131269		"Anemia, sideroblastic, with ataxia, 301310 (3), X-linked recessive"	Abcb7 (MGI:109533)			
chrX	75156378	75304896	Xq13.3	Xq13.3		300656	UPRT	"Uracil phosphoribosyltransferase, S. cerevisiae, homolog of"	UPRT	139596	ENSG00000094841			Uprt (MGI:2685620)			
chrX	75368426	75523501	Xq13.3	Xq13.3		300576	"ZDHHC15, MRX91"	Zinc finger DHHC domain-containing protein 15	ZDHHC15	158866	ENSG00000102383	disruption of ZDHHC15 identified in 1 patient	"?Mental retardation, X-linked 91, 300577 (3), X-linked dominant"	Zdhhc15 (MGI:1915336)			
chrX	75582653	75586207	Xq13.3	Xq13.3		300956	BRAFP1	BRAF pseudogene 1	BRAFP1	286494							
chrX	75782987	75785243	Xq13.1	Xq13.3		300760	MAGEE2	"Melanoma antigen, family E, 2"	MAGEE2	139599	ENSG00000186675			Magee2 (MGI:2148316)			
chrX	76427652	76431352	Xq13.1	Xq13.3		300759	"MAGEE1, DAMAGE, KIAA1587"	"Melanoma antigen, family E, 1"	MAGEE1	57692	ENSG00000198934			Magee1 (MGI:2148149)			
chrX	76800000	99100000	Xq21			303110	"DELXq21, CXDELq21"	Chromosome Xq21 deletion syndrome				at least CHM and POU3F4 deleted	"Choroideremia, deafness, and mental retardation, 303110 (4), X-linked recessive"				
chrX	76800000	129500000	Xq21-q25			300557	PARK12	Parkinson disease-12	PARK12	677662		"max lod with DXS1106, DXS8055, DXS1001"	"{Parkinson disease 12}, 300557 (2)"				
chrX	77447674	77456521	Xq21.1	Xq21.1		300827	"FGF16, MF4"	Fibroblast growth factor 16	FGF16	8823	ENSG00000196468	previously mapped to 8q21.3	"Metacarpal 4-5 fusion, 309630 (3), X-linked recessive"	Fgf16 (MGI:1931627)			
chrX	77504877	77786268	Xq13	Xq21.1		300032	"ATRX, XH2, XNP, SHS, SFM1, MRXHF1"	ATR-X gene (helicase 2; X-linked nuclear protein)	ATRX	546	ENSG00000085224		"Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3); Alpha-thalassemia/mental retardation syndrome, 301040 (3), X-linked dominant; Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3), X-linked recessive"	Atrx (MGI:103067)			
chrX	77826363	77895567	Xq13.1-q13.2	Xq21.1		300715	"MAGT1, IAP, XMEN"	Magnesium transporter 1	MAGT1	84061	ENSG00000102158		"Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, 300853 (3)"	Magt1 (MGI:1914325)			
chrX	77899463	77905383	Xq21.1	Xq21.1		300885	"COX7B, LSDMCA2"	"Cytochrome c oxidase, subunit VIIb"	COX7B	1349	ENSG00000131174		"Linear skin defects with multiple congenital anomalies 2, 300887 (3), X-linked dominant"	Cox7b (MGI:1913392)			
chrX	77910655	78050394	Xq12-q13	Xq21.1		300011	"ATP7A, MNK, MK, OHS, SMAX3"	"ATPase, Cu++ transporting, alpha polypeptide"	ATP7A	538	ENSG00000165240	"probably Xq13.2-q13.3, ~150kb prox. to PGK1"	"Menkes disease, 309400 (3), X-linked recessive; Occipital horn syndrome, 304150 (3), X-linked recessive; Spinal muscular atrophy, distal, X-linked 3, 300489 (3), X-linked recessive"	Atp7a (MGI:99400)			
chrX	77967960	77969637	Xq13.3	Xq21.1		300567	"PGAM4, PGAM3"	Phosphoglycerate mutase family member 4	PGAM4	441531	ENSG00000226784						
chrX	78104168	78126826	Xq13	Xq21.1		311800	"PGK1, PGKA"	Phosphoglycerate kinase-1	PGK1	5230	ENSG00000102144	"?Xq13.3; pseudogenes PGK1P1 on Xq, PGK1P2 on chr. 6"	"Phosphoglycerate kinase 1 deficiency, 300653 (3), X-linked recessive"	Pgk1 (MGI:97555)			
chrX	78129747	78139681	Xq13.1-q22.1	Xq21.1		300754	"TAF9B, TAF9L, TAFII31L"	"TAF9B RNA polymerase II, TATA box-binding protein-associated factor, 31kD"	TAF9B	51616	ENSG00000187325			Taf9b (MGI:3039562)			
chrX	78271467	78327690	Xq13-q21	Xq21.1		300201	"CYSLTR1, CYSLT1"	Cysteinyl leukotriene receptor 1	CYSLTR1	10800	ENSG00000173198			Cysltr1 (MGI:1926218)			
chrX	78747657	78758713	Xq13-q21.1	Xq21.1		300086	"LPAR4, LPA4, P2RY9, P2Y9, GPR23"	Lysophosphatidic acid receptor 4	LPAR4	2846	ENSG00000147145			Lpar4 (MGI:1925384)			
chrX	78945331	78963726	Xq21.1	Xq21.1		300529	"P2RY10, P2Y10"	"Purinergic receptor P2Y, G protein-coupled, 10"	P2RY10	27334	ENSG00000078589			P2ry10 (MGI:1926076)			
chrX	79170971	79172228	Xq21.1	Xq21.1		300903	"GPR174, GPCR17"	G protein-coupled receptor 174	GPR174	84636	ENSG00000147138			Gpr174 (MGI:2685222)			
chrX	79360383	79367551	Xq13.3-q21.2	Xq21.1		300222	"ITM2A, E25A"	Integral membrane protein 2A	ITM2A	9452	ENSG00000078596			Itm2a (MGI:107706)			
chrX	80014755	80031768	Xq12-q21	Xq21.1		300307	"TBX22, CPX, ABERS"	T-box 22	TBX22	50945	ENSG00000122145	1 ABERS family identified with mutation	"?Abruzzo-Erickson syndrome, 302905 (3), X-linked; Cleft palate with ankyloglossia, 303400 (3), X-linked"	Tbx22 (MGI:2389465)			
chrX	80335438	80446884	Xq21.1	Xq21.1		300976	FAM46D	"Family with sequence similarity 46, member D"	FAM46D	169966	ENSG00000174016			Fam46d (MGI:2685223)			
chrX	80669487	80809735	Xq13	Xq21.1		300553	"BRWD3, MRX93"	Bromodomain-and WD repeat-containing protein 3	BRWD3	254065	ENSG00000165288		"Mental retardation, X-linked 93, 300659 (3), X-linked recessive"	Brwd3 (MGI:3029414)			
chrX	81113700	81201941	Xq13	Xq21.1		300385	NSBP1	Nucleosomal binding protein 1	HMGN5	79366	ENSG00000198157						
chrX	81201803	81298546	Xq13.3	Xq21.1		300190	SH3BGR	SH3-binding domain glutamic acid-rich protein-like	SH3BGRL	6451	ENSG00000131171			Sh3bgrl (MGI:1930849)			
chrX	83508260	83509766	Xq21.1	Xq21.1		300039	"POU3F4, DFN3, DFNX2"	"POU domain, class 3, transcription factor 4"	POU3F4	5456	ENSG00000196767		"Deafness, X-linked 2, 304400 (3), X-linked recessive"	Pou3f4 (MGI:101894)			
chrX	83861125	83886699	Xq21.1	Xq21.1		300768	CYLC1	Cylicin 1	CYLC1	1538	ENSG00000183035						
chrX	84058345	84187934	Xq21	Xq21.1		300303	"RPS6KA6, RSK4"	"Ribosomal protein S6 kinase, 90kD, 6"	RPS6KA6	27330	ENSG00000072133			Rps6ka6 (MGI:1914321)			
chrX	84317873	84502577	Xq21.1	Xq21.1		300994	"HDX, CXorf43"	Highly divergent homeobox	HDX	139324	ENSG00000165259			Hdx (MGI:2685226)			
chrX	85003851	85093316	Xq21.2	Xq21.1		300955	"APOOL, FAM121A, Cxorf33"	Apolipoprotein O-like	APOOL	139322	ENSG00000155008			Apool (MGI:1915367)			
chrX	85243819	85273361	Xq21.1-q21.3	Xq21.1		314990	"ZNF711, ZNF6, CMPX1, MRX97"	Zinc finger protein-711	ZNF711	7552	ENSG00000147180		"Mental retardation, X-linked 97, 300803 (3), X-linked"	Zfp711 (MGI:3045342)			
chrX	85277388	85379742	Xq21	Xq21.1		300603	"FLJ22792, POF1B, POF2B"	FLJ22792 gene	POF1B	79983	ENSG00000124429	mutation identified in 1 POF2B family	"?Premature ovarian failure 2B, 300604 (3), X-linked recessive"	Pof1b (MGI:1916943)			
chrX	85861179	86047564	Xq21.2	Xq21.2		300390	"CHM, TCD"	Rab escort protein 1	CHM	1121	ENSG00000188419		"Choroideremia, 303100 (3), X-linked dominant"	Chm (MGI:892979)			
chrX	86148450	86832601	Xq21.3	Xq21.2		300608	DACH2	"Dachshund, Drosophila, homolog of, 2"	DACH2	117154	ENSG00000126733			Dach2 (MGI:1890446)			
chrX	87000000	99100000	Xq21.3			300756	AD16	Alzheimer disease 16		100271718		associated with rs5984894	"{Alzheimer disease 16}, 300756 (2)"				
chrX	87517711	87670049	Xq21.3	Xq21.31		300348	KLHL4	Kelch-like 4	KLHL4	56062	ENSG00000102271			Klhl4 (MGI:2442829)			
chrX	89921940	89922882	Xp21.3	Xq21.31		300411	"TGIF2LX, TGIFLX"	"Transforming growth factor-beta-induced factor 2-like, X-linked"	TGIF2LX	90316	ENSG00000153779			"Tgif2lx2,Tgif2lx1 (MGI:3800824,MGI:2387796)"			
chrX	91434597	91438583	Xq21.3	Xq21.31		300407	"PABPC5, PABP5"	"Polyadenylate-binding protein, cytoplasmic, 5"	PABPC5	140886	ENSG00000174740			Pabpc5 (MGI:2136401)			
chrX	91779309	92623229	Xq21.3	Xq21.31		300246	"PCDH11X, PCDH11, PCDHX"	"Protocadherin 11, X-linked"	PCDH11X	27328	ENSG00000102290			Pcdh11x (MGI:2442849)			
chrX	93670925	93673682	Xq21.3-q22	Xq21.32		300117	NAP1L3	Nucleosome assembly protein 1-like 3	NAP1L3	4675	ENSG00000186310			Nap1l3 (MGI:1859565)			
chrX	94300000	117400000	Xq21.33-q23			300861	MRXSCS	"Mental retardation, X-linked, syndromic, Chudley-Schwartz type"		100820761		max lod at DXS1120	"Mental retardation, X-linked, syndromic, Chudley-Schwartz type, 300861 (2), X-linked recessive"				
chrX	96684662	97600597	Xq22	Xq21.33		300108	"DIAPH2, DIA, POF2A"	"Diaphanous, Drosophila, homolog of, 2"	DIAPH2	1730	ENSG00000147202	mutation identified in 1 POF2A family	"?Premature ovarian failure 2A, 300511 (3), X-linked dominant"				
chrX	96883907	96885466	Xq21.33	Xq21.33		300767	RPA4	Replication protein A4	RPA4	29935	ENSG00000204086						
chrX	97528363	97564534	Xq21-q22	Xq21.33		300347	EPAG	Early lymphoid activation gene	DIAPH2-AS1	10824							
chrX	99100000	156040895	Xq22-q28			301201	"AI1E2, AIH3"	"Amelogenesis imperfecta, hypomaturation or hypoplastic type, X-linked 2"	AIH3	201			"?Amelogenesis imperfecta, type IE, X-linked 2, 301201 (2), X-linked"				
chrX	100291643	100410272	Xq22	Xq22.1		300460	"PCDH19, KIAA1313, EFMR, EIEE9"	Protocadherin 19	PCDH19	57526	ENSG00000165194		"Epileptic encephalopathy, early infantile, 9, 300088 (3), X-linked"	Pcdh19 (MGI:2685563)			
chrX	100584792	100599884	Xq22	Xq22.1		300459	"TNMD, TEM, CHM1L"	Tenomodulin	TNMD	64102	ENSG00000000005			Tnmd (MGI:1929885)			
chrX	100627107	100637103	Xq22	Xq22.1		300191	"TSPAN6, TM4SF6"	Tetraspanin 6	TSPAN6	7105	ENSG00000000003			Tspan6 (MGI:1926264)			
chrX	100644165	100671298	Xq21.33-q23	Xq22.1		300642	"SRPX2, SRPUL, RESDX"	"SUSHI repeat-containing protein, X-linked, 2"	SRPX2	27286	ENSG00000102359	mutation identified in 1 RESDX family	"?Rolandic epilepsy, mental retardation, and speech dyspraxia, 300643 (3)"	Srpx2 (MGI:1916042)			
chrX	100671963	100732147	Xq21.33	Xq22.1		300723	SYTL4	Synaptotagmin-like 4	SYTL4	94121	ENSG00000102362			Sytl4 (MGI:1351606)			
chrX	100820358	100843533	Xq22.1	Xq22.1		300907	CSTF64	"Cleavage stimulation factor, 3-prime pre-RNA, subunit 2, 64kD"	CSTF2	1478	ENSG00000101811			Cstf2 (MGI:1343054)			
chrX	100843323	100874344	Xq22	Xq22.1		300225	"NOX1, MOX1, NOH1"	NADPH oxidase 1	NOX1	27035	ENSG00000007952			Nox1 (MGI:2450016)			
chrX	100886918	100957400	Xq22.1	Xq22.1		300684	"XKRX, XPLAC, XKR2, XRG2"	"X Kell blood group precursor-related, X-linked"	XKRX	402415	ENSG00000182489			Xkrx (MGI:3584011)			
chrX	101098158	101181846	Xq22	Xq22.1		300065	"FSHPRH1, LRPR1"	"FSH primary response, rat, homolog of, 1"	CENPI	2491	ENSG00000102384			Cenpi (MGI:2147897)			
chrX	101219785	101264496	Xq22	Xq22.1		300052	DRP2	Dystrophin-related protein 2	DRP2	1821	ENSG00000102385			Drp2 (MGI:107432)			
chrX	101268252	101293070	Chr.X	Xq22.1		300314	"TAF7L, TAF2Q"	"TAF7-like RNA polymerase II, TATA box-binding protein-associated factor, 50kD"	TAF7L	54457	ENSG00000102387			Taf7l (MGI:1921719)			
chrX	101345655	101348968	Xq22	Xq22.1		300356	"TIMM8A, DFN1, DDP, MTS, DDP1"	"Translocase of inner mitochondrial membrane 8, yeast, homolog of, A"	TIMM8A	1678	ENSG00000126953		"Mohr-Tranebjaerg syndrome, 304700 (3), X-linked recessive"	Timm8a1 (MGI:1353433)			
chrX	101349446	101390795	Xq21.3-q22	Xq22.1		300300	"BTK, AGMX1, IMD1, XLA, AT"	Bruton agammaglobulinemia tyrosine kinase	BTK	695	ENSG00000010671		"Agammaglobulinemia and isolated hormone deficiency, 307200 (3), X-linked recessive; Agammaglobulinemia, X-linked 1, 300755 (3), X-linked recessive"	Btk (MGI:88216)			
chrX	101390889	101396153	Xq22.1	Xq22.1		300902	"RPL36A, RPL44"	Ribosomal protein L36A	RPL36A	6173	ENSG00000241343						
chrX	101397790	101408012	Xq22	Xq22.1		300644	GLA	"Galactosidase, alpha"	GLA	2717	ENSG00000102393		"Fabry disease, 301500 (3), X-linked; Fabry disease, cardiac variant, 301500 (3), X-linked"	Gla (MGI:1347344)			
chrX	101408132	101414139	Xq22	Xq22.1		300610	"HNRNPH2, NRPH2, MRXSB"	Heterogeneous nuclear ribonucleoprotein H2	HNRNPH2	3188	ENSG00000126945	"second signal at 6q25.3-q26, pseudogene?"	"Mental retardation, X-linked, syndromic, Bain type, 300986 (3), X-linked dominant"	Hnrnph2 (MGI:1201779)			
chrX	101550530	101554699	Xq21.33-q22.2	Xq22.1		300362	"ARMCX1, ALEX1"	"Armadillo repeat containing, X-linked 1"	ARMCX1	51309	ENSG00000126947			Armcx1 (MGI:1925498)			
chrX	101623129	101631909	Xq21.33-q22.2	Xq22.1		300364	"ARMCX3, ALEX3"	"Armadillo repeat containing, X-linked 3"	ARMCX3	51566	ENSG00000102401			Armcx3 (MGI:1918953)			
chrX	101655280	101659890	Xq21.33-q22.2	Xq22.1		300363	"ARMCX2, ALEX2, KIAA0512"	"Armadillo repeat containing, X-linked 2"	ARMCX2	9823	ENSG00000184867			Armcx2 (MGI:1914666)			
chrX	101832111	101857576	Xq22.1	Xq22.1		300319	NXF5	Nuclear RNA export factor 5	NXF5	55998	ENSG00000126952						
chrX	101882287	101932134	Xq22.1	Xq22.1		301007	"ZMAT1, KIAA1789"	"Zinc finger, matrin-type 1"	ZMAT1	84460	ENSG00000166432			Zmat1 (MGI:2442284)			
chrX	102153706	102156013	Xq22.1	Xq22.1		300693	"BEX5, NGFRAP1L1"	BEX family member 5	BEX5	340542	ENSG00000184515						
chrX	102247099	102326719	Chr.X	Xq22.1		300315	NXF2	Nuclear RNA export factor 2	NXF2	56001	ENSG00000269405			Nxf2 (MGI:1933192)			
chrX	102513681	102516770	Xq22.1	Xq22.1		300939	"TMSB15A, TMSB15, TMSNB"	"Thymosin, beta-15A"	TMSB15A	11013	ENSG00000158164						
chrX	102549964	102571692	Xq22.1-q22.3	Xq22.1		300318	NXF4	Nuclear RNA export factor 4	NXF4	55999							
chrX	102651365	102659082	Xq22	Xq22.1		300417	"GPRASP1, GASP, KIAA0443"	G protein-coupled receptor-associated sorting protein 1	GPRASP1	9737	ENSG00000198932	conflicting assignment to chr.9		Gprasp1 (MGI:1917418)			
chrX	102712175	102717732	Xq22.1	Xq22.1		300969	"GPRASP2, GASP2"	G protein-coupled receptor-associated sorting protein 2	GPRASP2	114928	ENSG00000158301						
chrX	102720713	102752440	Xq22.1	Xq22.1		300921	"BHLHB9, P60TRP, KIAA1701"	"Basic helix-loop-helix domain-containing protein, class B, 9"	BHLHB9	80823	ENSG00000198908			Bhlhb9 (MGI:1917487)			
chrX	102937271	102938299	Xq22.2	Xq22.1		300405	"RAB40AL, RLGP, MRXSMP"	"Ras-associated protein, RAB40A-like"	RAB40AL	282808	ENSG00000102128						
chrX	103062652	103064239	Xq22.1-q22.2	Xq22.1		300690	BEX1	Brain-expressed X-linked gene 1	BEX1	55859	ENSG00000133169			Bex2 (MGI:1338017)			
chrX	103075820	103093093	Xq21.3-q22.3	Xq22.1		300316	NXF3	Nuclear RNA export factor 3	NXF3	56000	ENSG00000147206			Nxf3 (MGI:2685230)			
chrX	103215091	103217199	Xq22.2	Xq22.1		300692	BEX4	BEX family member 4	BEX4	56271	ENSG00000102409			Bex4 (MGI:3606746)			
chrX	103300000	138900000	Xq22.2-q26			300324	MRX53	"Mental retardation, X-linked-53"	MRX53	4416			"Mental retardation, X-linked 53, 300324 (2), X-linked recessive"				
chrX	103309345	103311045	Xq22	Xq22.2		300691	BEX2	Brain-expressed X-linked gene 2	BEX2	84707	ENSG00000133134						
chrX	103330185	103332325	Xq22.1-q22.3	Xq22.2		300771	TCEAL7	Transcription elongation factor A-like 7	TCEAL7	56849	ENSG00000182916			Tceal7 (MGI:1915746)			
chrX	103376322	103378163	Xq22.1-q23	Xq22.2		300361	"NGFRAP1, BEX3, NADE, DXS6984E"	Nerve growth factor receptor (TNFRSF16) associated protein 1	BEX3	27018	ENSG00000166681			Bex3 (MGI:1338016)			
chrX	103628719	103630952	Xq22.1	Xq22.2		300237	"TCEAL1, P21, SIIR"	Transcription elongation factor A-like 1	TCEAL1	9338	ENSG00000172465			Tceal1 (MGI:2385317)			
chrX	103675497	103688157	Xq22	Xq22.2		300409	"MORFL2, MRGX, KIAA0026"	Mortality factor 4-like 2	MORF4L2	9643	ENSG00000123562			Morf4l2 (MGI:1927167)			
chrX	103776323	103832281	Xq22.1-q22.3	Xq22.2		300285	"RAB9B, RAB9L"	RAS-associated protein RAB9B	RAB9B	51209	ENSG00000123570			Rab9b (MGI:2442454)			
chrX	103776505	103792618	Xq22	Xq22.2		300401	"PLP1, PMD, HLD1, SPG2"	Proteolipid protein 1	PLP1	5354	ENSG00000123560		"Pelizaeus-Merzbacher disease, 312080 (3), X-linked recessive; Spastic paraplegia 2, X-linked, 312920 (3), X-linked recessive"	Plp1 (MGI:97623)			
chrX	103918895	103974425	Xq22.2	Xq22.2		301011	TMSB15B	"Thymosin, beta-15B"	TMSB15B	286527	ENSG00000158427	opposite strand relative to TMSB15A					
chrX	104011146	104013686	Xq22.2	Xq22.2		300507	H2BFWT	"H2B histone family, member W, testis-specific"	H2BFWT	158983	ENSG00000123569						
chrX	104099213	104157026	Xq22.2	Xq22.2		300941	SLC25A53	"Solute carrier family 25, member 53"	SLC25A53	401612	ENSG00000269743			Slc25a53 (MGI:1914312)			
chrX	104250037	104254917	Xq22.1-q22.3	Xq22.2		300154	"ESX1L, ESXR1"	ESX1-like protein	ESX1	80712	ENSG00000123576						
chrX	104500000	109400000	Xq22.3			300194	"AMMEC, DELXq22.3, CXDELq22.3"	"Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis (AMME complex)"				contiguous gene deletion syndrome	"Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis, 300194 (4)"				
chrX	104500000	109400000	Xq22.3			300581	FGS5	FG syndrome 5	FGS5	780900			"FG syndrome 5, 300581 (2)"				
chrX	104566314	105769728	Xq22	Xq22.3		300277	IL1RAPL2	Interleukin 1 receptor accessory protein-like 2	IL1RAPL2	26280	ENSG00000189108			Il1rapl2 (MGI:1913106)			
chrX	105218928	105220692	Chr.X	Xq22.3		300312	TEX13A	Testis-expressed gene 13A	TEX13A	56157	ENSG00000268629			Tex13a (MGI:1915194)			
chrX	105821941	105958609	Xq22.3	Xq22.3		300791	"NRK, NESK"	NIK-related kinase	NRK	203447	ENSG00000123572			Nrk (MGI:1351326)			
chrX	106032438	106038726	Xq22.2	Xq22.3		314200	"TBG, TBGQTL"	Thyroxine-binding globulin	SERPINA7	6906	ENSG00000123561		"[Thyroxine-binding globulin QTL], 300932 (3)"	Serpina7 (MGI:3041197)			
chrX	106693837	106797015	Xq22.3	Xq22.3		300439	"RNF128, GRAIL"	Ring finger protein 128	RNF128	79589	ENSG00000133135			Rnf128 (MGI:1914139)			
chrX	106900062	106903330	Xq22.3	Xq22.3		300575	RIPPLY1	"Ripply1, zebrafish, homolog of"	RIPPLY1	92129	ENSG00000147223						
chrX	106900163	106930860	Xq22.3-q23	Xq22.3		300520	CLDN2	Claudin 2	CLDN2	9075	ENSG00000165376			Cldn2 (MGI:1276110)			
chrX	106940299	107000243	Xq22.3	Xq22.3		300970	"MORC4, ZCW4, ZCWCC2"	MORC family CW-type zinc finger protein 4	MORC4	79710	ENSG00000133131			Morc4 (MGI:1922996)			
chrX	107206628	107244242	Xq22.3	Xq22.3		300933	"PIH1D3, CILD36"	PIH1 domain-containing protein 3	PIH1D3	139212	ENSG00000080572		"Ciliary dyskinesia, primary, 36, X-linked, 300991 (3), X-linked recessive"	"Pih1h3b,Pih1d3 (MGI:3607720,MGI:1921958)"			
chrX	107272463	107276558	Xq22-q23	Xq22.3		310310	MYCL2	MYCL-related processed gene	MYCLP1	4611		pseudogene on Xq27.3					
chrX	107522449	107605263	Xq22.3	Xq22.3		301005	"FRMPD3, KIAA1817"	FERM- and PDZ domain-containing protein 3	FRMPD3	84443	ENSG00000147234						
chrX	107628423	107651025	Xq22-q24	Xq22.3		311850	"PRPS1, CMTX5, DFNX1, DFN2"	Phosphoribosyl pyrophosphate synthetase-1	PRPS1	5631	ENSG00000147224		"Arts syndrome, 301835 (3), X-linked recessive; Charcot-Marie-Tooth disease, X-linked recessive, 5, 311070 (3), X-linked recessive; Deafness, X-linked 1, 304500 (3), X-linked; Gout, PRPS-related, 300661 (3), X-linked recessive; Phosphoribosylpyrophosphate synthetase superactivity, 300661 (3), X-linked recessive"	Prps1 (MGI:97775)			
chrX	107713220	107777328	Xq22.2	Xq22.3		300506	"TSC22D3, DSIPI, GILZ"	"TSC22 domain family, member 3"	TSC22D3	1831	ENSG00000157514			Tsc22d3 (MGI:1196284)			
chrX	107820452	107931636	Xq22	Xq22.3		300204	"MID2, MRX101"	Midline 2	MID2	11043	ENSG00000080561	mutation identified in 1 MRX101 family	"?Mental retardation, X-linked 101, 300928 (3), X-linked recessive"	Mid2 (MGI:1344333)			
chrX	107980863	107982369	Chr.X	Xq22.3		300313	TEX13B	Testis-expressed gene 13B	TEX13B	56156	ENSG00000170925			Tex13b (MGI:1890544)			
chrX	108018885	108079183	Xq22.1-q22.3	Xq22.3		300620	"VSIG1, GPA34"	V-set and immunoglobulin domains-containing protein 1	VSIG1	340547	ENSG00000101842			Vsig1 (MGI:1926039)			
chrX	108084204	108091643	Xq22.3	Xq22.3		300880	"PSMD10, p28"	"Proteasome 26S subunit, non-ATPase, 10"	PSMD10	5716	ENSG00000101843			Psmd10 (MGI:1858898)			
chrX	108091666	108154670	Xq22	Xq22.3		300663	"ATG4A, APG4A, AUTL2"	"Autophagy 4, S. cerevisiae, homolog of, A"	ATG4A	115201	ENSG00000101844			Atg4a (MGI:2147903)			
chrX	108155606	108439496	Xq22.3	Xq22.3		303631	"COL4A6, DELXq22.3, CXDELq22.3, DFNX6"	"Collagen IV, alpha-6 polypeptide"	COL4A6	1288	ENSG00000197565	mutation identified in 1 DFNX6 family	"?Deafness, X-linked 6, 300914 (3), X-linked recessive"	Col4a6 (MGI:2152695)			
chrX	108439843	108697544	Xq22.3	Xq22.3		303630	"COL4A5, ATS, ASLN"	"Collagen IV, alpha-5 polypeptide"	COL4A5	1287	ENSG00000188153	diffuse leiomyomatosis with Alport syndrome = contiguous gene syndrome with COL4A6	"Alport syndrome, 301050 (3), X-linked dominant"	Col4a5 (MGI:88456)			
chrX	108719948	108736583	Xq22.3	Xq22.3		300904	IRS4	Insulin receptor substrate 4	IRS4	8471	ENSG00000133124						
chrX	109372060	109482055	Xq22	Xq22-q23		300041	"GUCY2F, GUC2F"	Guanylate cyclase 2F	GUCY2F	2986	ENSG00000101890			Gucy2f (MGI:105119)			
chrX	109400000	138900000	Xq23-q26			300464	CHDS3	"Coronary heart disease, susceptibility to, 3"		387573			"{Coronary heart disease, susceptibility to, 3}, 300464 (2)"				
chrX	109400000	117400000	Xq23			300711	IHPS4	"Pyloric stenosis, infantile hypertrophic, 4"		100188772		max lod at rs3027802	"Pyloric stenosis, infantile hypertrophic, 4, 300711 (2)"				
chrX	109400000	121800000	Xq23-q24			300046	MRX23	"Mental retardation, X-linked-23"	MRX23	4387		"other MRX in same region MRX27, MRX30, MRX35, MRX47, MRX80"	"Mental retardation, X-linked 23, 300046 (2), X-linked"				
chrX	109400000	143000000	Xq23-q27.2			300613	MYP13	Myopia 13	MYP13	677764		between DXS1210 and DXS1227	"Myopia 13, 300613 (2)"				
chrX	109535780	109544697	Xq23	Xq23		300320	NXT2	NTF2-related export protein 2	NXT2	55916	ENSG00000101888			Nxt2 (MGI:2147914)			
chrX	109623699	109625167	Xq22.3	Xq23		300328	KCNE1L	"Potassium voltage-gated channel, Isk-related family, member 1-like"	KCNE5	23630	ENSG00000176076			Kcne1l (MGI:1913490)			
chrX	109641329	109733402	Xq22.3	Xq23		300157	"ACSL4, FACL4, ACS4, MRX63"	Acyl-CoA synthetase long-chain family member 4	ACSL4	2182	ENSG00000068366		"Mental retardation, X-linked 63, 300387 (3), X-linked dominant"	Acsl4 (MGI:1354713)			
chrX	110194185	110440232	Xq22.3	Xq23		300195	"AMMECR1, MFHIEN"	"Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis chromosomal region gene 1"	AMMECR1	9949	ENSG00000101935		"Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 (3), X-linked recessive"	Ammecr1 (MGI:1860206)			
chrX	110358100	110456333	Xq23	Xq23		300965	"RGAG1, MAR9, KIAA1318"	Retrotransposon GAG domain-containing protein 1	RTL9	57529	ENSG00000243978			Rtl9 (MGI:2685231)			
chrX	110673855	110796057	Xq22.1-q23	Xq23		300350	"CHRDL1, VOPT, MGC1"	Chordin-like 1	CHRDL1	91851	ENSG00000101938		"Megalocornea 1, X-linked, 309300 (3), X-linked recessive"	Chrdl1 (MGI:1933172)			
chrX	110944240	111227360	Xq23	Xq23		300142	"PAK3, MRX30, MRX47"	p21-activated kinase-3	PAK3	5063	ENSG00000077264		"Mental retardation, X-linked 30/47, 300558 (3), X-linked recessive"	Pak3 (MGI:1339656)			
chrX	111245098	111270545	Xq23	Xq23		300146	CAPN6	Calpain 6	CAPN6	827	ENSG00000077274			Capn6 (MGI:1100850)			
chrX	111293778	111412231	Xq22.3-q23	Xq23		300121	"DCX, DBCN, LISX"	Doublecortin	DCX	1641	ENSG00000077279		"Lissencephaly, X-linked, 300067 (3), X-linked; Subcortical laminal heterotopia, X-linked, 300067 (3), X-linked"	Dcx (MGI:1277171)			
chrX	111680740	111764163	Xq23	Xq23		300776	"ALG13, GLT28D1, CDG1S, EIEE36"	"Alg13, S. cerevisiae, homolog of"	ALG13	79868	ENSG00000101901	mutation identified in 1 CDG1S male patient	"?Congenital disorder of glycosylation, type Is, 300884 (3), X-linked dominant; Epileptic encephalopathy, early infantile, 36, 300884 (3), X-linked dominant"				
chrX	111774313	112082942	Xq23	Xq23		300334	"TRPC5, TRP5"	Transient receptor potential channel 5	TRPC5	7224	ENSG00000072315			Trpc5 (MGI:109524)			
chrX	112630650	112680177	Xq23	Xq23		300566	LHFPL1	LHFP-like protein 1	LHFPL1	340596	ENSG00000182508			Lhfpl1 (MGI:1891214)			
chrX	112774876	112840945	Chr.X	Xq23		300410	"AMOT, KIAA1071"	Angiomotin	AMOT	154796	ENSG00000126016			Amot (MGI:108440)			
chrX	113616299	113618152	Xq23	Xq23		300901	XACT	"Active X chromosome-coating transcript, noncoding"	XACT	105463123							
chrX	114584077	114910060	Xq24	Xq23		312861	HTR2C	5-hydroxytryptamine (serotonin) receptor-2C	HTR2C	3358	ENSG00000147246	formerly HTR1C		Htr2c (MGI:96281)			
chrX	114823453	114823563	Xq23	Xq23		300686	"MIR448, MIRN448"	Micro RNA 448	MIR448	554212							
chrX	115003974	115017643	Xq24	Xq23		300130	IL13RA2	"Interleukin-13 receptor, alpha-2"	IL13RA2	3598	ENSG00000123496			Il13ra2 (MGI:1277954)			
chrX	115289716	115307555	Xq23	Xq23		300616	LUZP4	Leucine zipper protein 4	LUZP4	51213	ENSG00000102021						
chrX	115560849	115650860	Xq23	Xq23		300131	"PLS3, BMND18"	Plastin 3	PLS3	5358	ENSG00000102024		"Bone mineral density QTL18, osteoporosis, 300910 (3), X-linked dominant"	Pls3 (MGI:104807)			
chrX	115840395	115969110	Xq23	Xq23		301004	DANT2	"DXZ4-associated noncoding transcript 2, distal"	DANT2	642776							
chrX	115840963	115905526	Xq23	Xq23		301001	DANT1	"DXZ4-associated noncoding transcript 1, proximal"	DANT1	106029310							
chrX	116170704	116174971	Xq23	Xq23		300034	AGTR2	Angiotensin receptor 2	AGTR2	186	ENSG00000180772			Agtr2 (MGI:87966)			
chrX	116436578	116461457	Xq23-q24	Xq23		300444	"SLC6A14, OBX, BMIQ11"	"Solute carrier family 6 (neurotransmitter transporter), member 14"	SLC6A14	11254	ENSG00000268104		"{Obesity, susceptibility to, BMIQ11}, 300306 (3)"	Slc6a14 (MGI:1890216)			
chrX	116461685	116463032	Xq22	Xq23		300625	"KKLC1, CXorf61"	Kita-Kyushu lung cancer antigen 1	CT83	203413	ENSG00000204019						
chrX	117400000	138900000	Xq24-q26			300700	"ADFN, ALDS"	Albinism-deafness syndrome	ADFN	122		~8cM proximal to F9	"Albinism-deafness syndrome, 300700 (2), X-linked"				
chrX	117400000	148000000	Xq24-q27			301845	BZX	Bazex syndrome		8255			"Bazex syndrome, 301845 (2), X-linked dominant"				
chrX	117400000	156040895	Xq24-qter			304730	CND	Corneal dermoids		8231			"Dermoids of cornea, 304730 (2), X-linked"				
chrX	117400000	121800000	Xq24			300360	MRSS	"Mental retardation, X-linked, with short stature"					"Mental retardation, X-linked, with short stature, 300360 (2)"				
chrX	117400000	129500000	Xq24-q25			300518	MRX82	"Mental retardation, X-linked 82"	MRX82	378484		between DXS6805 and DXS7346	"Mental retardation, X-linked 82, 300518 (2), X-linked recessive"				
chrX	117400000	121800000	Xq24			300852	MRX88	"Mental retardation, X-linked 88"		105463129			"Mental retardation, X-linked 88, 300852 (2), X-linked"				
chrX	117400000	141200000	Xq24-q27.1			300245	"PTOS2, PTOSX"	"Ptosis, hereditary congenital 2"		54115			"Ptosis, hereditary congenital 2, 300245 (2), X-linked dominant"				
chrX	117400000	129500000	Xq24-q25			300378	RRDX	Radial ray deficiency		266719			"Radial ray deficiency, 300378 (2)"				
chrX	117400000	129500000	Xq24-q25			300750	SPG34	"Spastic paraplegia 34, X-linked"	SPG34	724110		max lod at DXS8057	"Spastic paraplegia 34, X-linked, 300750 (2), X-linked recessive"				
chrX	117400000	129500000	Xq24-q25			300591	STQTL6	Stature quantitative trait locus 6		100037264		max lod at DXS8067	"{Stature QTL 6}, 300591 (2)"				
chrX	117897812	118117339	Xq24	Xq24		300655	"KLHL13, KIAA1309"	Kelch-like 13	KLHL13	90293	ENSG00000003096			Klhl13 (MGI:1914705)			
chrX	118495663	118686159	Xq24	Xq24		300681	"DOCK11, ACG, ZIZ2"	Dedicator of cytokinesis 11	DOCK11	139818	ENSG00000147251			Dock11 (MGI:1923224)			
chrX	118726953	118794532	Chr.X	Xq24		300119	IL13RA1	"Interleukin-13 receptor, alpha-1"	IL13RA1	3597	ENSG00000131724			Il13ra1 (MGI:105052)			
chrX	118823742	118826972	Xq24	Xq24		300701	"ZCCHC12, SIZN1"	Zinc finger CCHC domain-containing protein 12	ZCCHC12	170261	ENSG00000174460			Zcchc12 (MGI:1919943)			
chrX	119078634	119151082	Xq24	Xq24		300995	KIAA1210	Kiaa1210 gene	KIAA1210	57481	ENSG00000250423						
chrX	119236244	119244465	Xq22-q24	Xq24		300435	PGRMC1	Progesterone receptor membrane component 1	PGRMC1	10857	ENSG00000101856			Pgrmc1 (MGI:1858305)			
chrX	119399294	119454477	Xq24	Xq24		300641	SLC25A43	"Solute carrier family 25, member 43"	SLC25A43	203427	ENSG00000077713			Slc25a43 (MGI:2684854)			
chrX	119468399	119471395	Xq24-q26	Xq24		300150	"SLC25A5, ANT2, T3"	"Solute carrier family 25 (mitochondrial carrier), member 5 (adenine nucleotide translocator-2, fibroblast)"	SLC25A5	292	ENSG00000005022			Slc25a5 (MGI:1353496)			
chrX	119574466	119584428	Xq24	Xq24		312180	"UBE2A, RAD6A, MRXSN, MRXS30"	Ubiquitin-conjugating enzyme E2A (RAD6 homolog)	UBE2A	7319	ENSG00000077721		"Mental retardation, X-linked syndromic, Nascimento-type, 300860 (3), X-linked recessive"	Ube2a (MGI:102959)			
chrX	119588336	119606463	Xq24	Xq24		300440	"NKRF, NRF"	NFKB-repressing factor	NKRF	55922	ENSG00000186416			Nkrf (MGI:1924536)			
chrX	119615723	119693369	Xq24	Xq24		300683	"SEPT6, SEP2, KIAA0128"	Septin 6	6-Sep	23157	ENSG00000125354			Sept6 (MGI:1888939)			
chrX	119786503	119791658	Xq24	Xq24		300899	RPL39	Ribosomal protein L39	RPL39	6170	ENSG00000198918			Rpl39 (MGI:1914498)			
chrX	119805310	119853027	Xq25-q26	Xq24		300298	"UPF3B, RENT3B, MRXS14"	"UPF3 regulator of nonsense transcripts, yeast, homolog of, B"	UPF3B	65109	ENSG00000125351		"Mental retardation, X-linked, syndromic 14, 300676 (3), X-linked recessive"	Upf3b (MGI:1915384)			
chrX	119870531	119871827	Xq24	Xq24		300951	"RNF113A, ZNF183, TTD5"	RING finger protein 113A	RNF113A	7737	ENSG00000125352	mutation identified in 1 TTD5 family	"?Trichothiodystrophy 5, nonphotosensitive, 300953 (3), X-linked dominant"	Rnf113a2 (MGI:1913631)			
chrX	119871770	119876665	Xq24	Xq24		300078	"NDUFA1, MWFE"	"NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kD"	NDUFA1	4694	ENSG00000125356		"Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial"	Ndufa1 (MGI:1929511)			
chrX	119895972	119920715	Xq24	Xq24		300462	"AKAP14, AKAP28"	A-kinase anchor protein 14	AKAP14	158798	ENSG00000186471			Akap14 (MGI:3618288)			
chrX	119925049	119943771	Xq24	Xq24		300766	NKAP	NFKB-activating protein	NKAP	79576	ENSG00000101882			Nkap (MGI:1914300)			
chrX	120010716	120015550	Xq24	Xq24		300973	RHOXF1P1	"RHOX homeobox family member 1, pseudogene 1"	RHOXF1P1	101928941							
chrX	120109048	120117650	Xq24	Xq24		300446	"RHOXF1, OTEX, PEPP1"	"RHOX homeobox family, member 1"	RHOXF1	158800	ENSG00000101883						
chrX	120158534	120165625	Xq24	Xq24		300447	"RHOXF2, PEPP2"	"RHOX homeobox family, member 2"	RHOXF2	84528	ENSG00000131721						
chrX	120250751	120258395	Xq23	Xq24		300329	"ZBTB33, KAISO"	Zinc finger- and BTB domain-containing protein 33	ZBTB33	10009	ENSG00000177485			Zbtb33 (MGI:1927290)			
chrX	120426147	120469348	Xq24	Xq24		309060	"LAMP2, LAMPB, LGP110"	Lysosome-associated membrane protein-2	LAMP2	3920	ENSG00000005893		"Danon disease, 300257 (3), X-linked dominant"	Lamp2 (MGI:96748)			
chrX	120524588	120575828	Xq23	Xq24		300304	"CUL4B, MRXSC, MRXHF2, SFM2, MRXS15"	Cullin-4B	CUL4B	8450	ENSG00000158290		"Mental retardation, X-linked, syndromic 15 (Cabezas type), 300354 (3), X-linked recessive"	Cul4b (MGI:1919834)			
chrX	120603888	120621158	Xq22-q24	Xq24		300587	"MCTS1, MCT1"	Malignant T-cell amplified sequence 1	MCTS1	28985	ENSG00000232119			Mcts1 (MGI:1916245)			
chrX	120625673	120630149	Xq23	Xq24		300611	"C1GALT1C1, COSMC, C1GALT2, TNPS"	C1GALT1-specific chaperone 1	C1GALT1C1	29071	ENSG00000171155		"Tn polyagglutination syndrome, somatic, 300622 (3)"	C1galt1c1 (MGI:1913493)			
chrX	120872551	120875924	Xq24	Xq24		300790	"CT47B1, CT47A13"	"Cancer/testis antigen family 47, member B1"	CT47B1	643311	ENSG00000236446						
chrX	120933839	120937259	Xq24	Xq24		300592	"CT47A11, LOC255313"	"Cancer/testis antigen family 47, member A11"	CT47A11	255313	ENSG00000226929						
chrX	120938700	120942120	Xq24	Xq24		300789	CT47A10	"Cancer/testis antigen family 47, member A10"	CT47A10	728036	ENSG00000224089						
chrX	120943560	120946980	Xq24	Xq24		300788	CT47A9	"Cancer/testis antigen family 47, member A9"	CT47A9	728042	ENSG00000226600						
chrX	120948421	120951841	Xq24	Xq24		300787	CT47A8	"Cancer/testis antigen family 47, member A8"	CT47A8	728049	ENSG00000230347						
chrX	120953281	120956599	Xq24	Xq24		300786	CT47A7	"Cancer/testis antigen family 47, member A7"	CT47A7	653282	ENSG00000228517						
chrX	120958164	120961587	Xq24	Xq24		300785	CT47A6	"Cancer/testis antigen family 47, member A6"	CT47A6	728062	ENSG00000226023						
chrX	120963025	120966445	Xq24	Xq24		300784	CT47A5	"Cancer/testis antigen family 47, member A5"	CT47A5	728072	ENSG00000237957						
chrX	120967885	120971305	Xq24	Xq24		300783	CT47A4	"Cancer/testis antigen family 47, member A4"	CT47A4	728075	ENSG00000230594						
chrX	120972745	120976165	Xq24	Xq24		300782	CT47A3	"Cancer/testis antigen family 47, member A3"	CT47A3	728082	ENSG00000236126						
chrX	120977605	120981025	Xq24	Xq24		300781	CT47A2	"Cancer/testis antigen family 47, member A2"	CT47A2	728090	ENSG00000242362						
chrX	120982465	120985885	Xq24	Xq24		300780	CT47A1	"Cancer/testis antigen family 45, member A1"	CT47A1	728096	ENSG00000236371						
chrX	121047607	121049941	Xq25	Xq24		300144	GLUD2	Glutamate dehydrogenase-2	GLUD2	2747	ENSG00000182890		"{Parkinson disease, age of onset, modifier}, 168600 (3), Isolated cases, Multifactorial"				
chrX	121800000	129500000	Xq25			300979	DUPXq25	Xq25 duplication syndrome					"Xq25 duplication syndrome, 300979 (4), X-linked"				
chrX	121800000	148000000	Xq25-q27			300660	LKMCD	Leukoencephalopathy with metaphyseal chondrodysplasia		100302058		between DXS8093 and DXS1232	"Leukoencephalopathy with metaphyseal chondrodysplasia, 300660 (2), X-linked recessive"				
chrX	121800000	141200000	Xq25-q27.1			300703	SCAX5	"Spinocerebellar ataxia, X-linked 5"		100188768		between DXS1047 and DXS1227	"Spinocerebellar ataxia, X-linked 5, 300703 (2), X-linked recessive"				
chrX	121800000	138900000	Xq25-q26			300179	SXI2	"X inactivation, familial skewed, 2"		117237			"X inactivation, familial skewed, 2, 300179 (2)"				
chrX	121800000	131300000	Xq25-q26.1			313850	"THAS, TAS"	Thoracoabdominal syndrome	THAS	7055			"Thoracoabdominal syndrome, 313850 (2), X-linked"				
chrX	121800000	129500000	Xq25			300779	XECD	"Corneal dystrophy, endothelial, X-linked"		100302510		between DXS8057 and DXS1047	"Corneal dystrophy, endothelial, X-linked, 300779 (2), X-linked dominant"				
chrX	123184242	123490914	Xq25-q26	Xq25		305915	"GRIA3, GLUR3, MRX94"	"Glutamate receptor, ionotropic, AMPA 3"	GRIA3	2892	ENSG00000125675		"Mental retardation, X-linked 94, 300699 (3), X-linked recessive"	Gria3 (MGI:95810)			
chrX	123600560	123733053	Xq25	Xq25		300395	"THOC2, THO2, MRX12, MRX35"	"THO complex 2 (Tho2, yeast, homolog of)"	THOC2	57187	ENSG00000125676		"Mental retardation, X-linked 12/35, 300957 (3), X-linked recessive"	Thoc2 (MGI:2442413)			
chrX	123859811	123913978	Xq25	Xq25		300079	"XIAP, BIRC4, API3, XLP2"	"Inhibitor of apoptosis, X-linked"	XIAP	331	ENSG00000101966		"Lymphoproliferative syndrome, X-linked, 2, 300635 (3), X-linked recessive"	Xiap (MGI:107572)			
chrX	123960559	124102655	Xq25	Xq25		300826	"STAG2, SA2"	Stromal antigen 2	STAG2	10735	ENSG00000101972			Stag2 (MGI:1098583)			
chrX	124346281	124373159	Xq25	Xq25		300490	"SH2D1A, LYP, IMD5, XLP, XLPD1"	SH2 domain protein 1A	SH2D1A	4068	ENSG00000183918	1cM from DXS42; no recombination with DXS37	"Lymphoproliferative syndrome, X-linked, 1, 308240 (3), X-linked recessive"	Sh2d1a (MGI:1328352)			
chrX	124375902	125204380	Xq25	Xq25		300588	"TENM1, ODZ1, TNM1"	Teneurin transmembrane protein 1	TENM1	10178	ENSG00000009694			Tenm1 (MGI:1345185)			
chrX	128050961	128052402	Xq25	Xq25		300487	"ACTRT1, ARPT1"	Actin-related protein T1	ACTRT1	139741	ENSG00000123165			Actrt1 (MGI:1920610)			
chrX	129446500	129523563	Xq26.1	Xq25-q26		300012	"SMARCA1, SNF2L1"	"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1"	SMARCA1	6594	ENSG00000102038			Smarca1 (MGI:1935127)			
chrX	129500000	148000000	Xq26-q27			300712	CFSS	Craniofacioskeletal syndrome		100188773			"?Craniofacioskeletal syndrome, 300712 (2), X-linked recessive, X-linked dominant"				
chrX	129500000	138900000	Xq26			302802	CMTX3	"Charcot-Marie-Tooth neuropathy, X-linked recessive, 3"	CMTX3	1254		between DXS984 and DXS8106	"Charcot-Marie-Tooth neuropathy, X-linked recessive, 3, 302802 (2), X-linked recessive"				
chrX	129500000	138900000	Xq26			309555	GUST	"Gustavson mental retardation syndrome (with microcephaly, optic atrophy, deafness)"		8258			"Gustavson syndrome, 309555 (2), X-linked"				
chrX	129500000	148000000	Xq26-q27			307700	"HPT, HPTX, HYPX"	Hypoparathyroidism	HPT	3258		?mutations in SOX3	"Hypoparathyroidism, X-linked, 307700 (2), X-linked"				
chrX	129500000	156040895	Xq26-qter			300076	INDX	"Immunoneurologic syndrome X-linked, of Woods, Black, and Norbury"		8259			"Woods-Black-Norbury syndrome, 300076 (2), X-linked dominant"				
chrX	129500000	138900000	Xq26			300372	MRX42	"Mental retardation, X-linked nonspecific, 42"	MRX42	4406		?pericentromeric region	"Mental retardation, X-linked 42, 300372 (2)"				
chrX	129500000	148000000	Xq26-q27			300155	RP24	Retinitis pigmentosa-24	RP24	6116			"Retinitis pigmentosa 24, 300155 (2)"				
chrX	129500000	138900000	Xq26			313350	"SHFM2, SHFD2"	"Split hand/foot malformation, type (ectrodactyly) 2"	SHFM2	6463			"Split hand/foot malformation 2, 313350 (2), X-linked"				
chrX	129532735	129592560	Xq26.1	Xq26.1		300535	"OCRL, LOCR, OCRL1, NPHL2"	Phosphatidylinositol polyphosphate 5-phosphatase (OCRL gene)	OCRL	4952	ENSG00000122126		"Dent disease 2, 300555 (3), X-linked recessive; Lowe syndrome, 309000 (3), X-linked recessive"	Ocrl (MGI:109589)			
chrX	129645258	129654955	Xq25-q26.3	Xq26.1		300297	APLN	Apelin	APLN	8862	ENSG00000171388			Apln (MGI:1353624)			
chrX	129738969	129769548	Xq25	Xq26.1		300145	"XPNPEP2, AEACEI"	X-prolyl aminopeptidase 2 (aminopeptidase P)	XPNPEP2	7512	ENSG00000122121		"{Angioedema induced by ACE inhibitors, susceptibility to}, 300909 (3)"	Xpnpep2 (MGI:2180001)			
chrX	129779915	129795200	Xq26.1	Xq26.1		300441	"SASH3, HACS2, CXorf9, SLY"	SAM and SH3 domain containing 3	SASH3	54440	ENSG00000122122			Sash3 (MGI:1921381)			
chrX	129803287	129843933	Xq26.1	Xq26.1		300646	"ZDHHC9, DHHC9, MRXSZ"	Zinc finger DHHC domain-containing protein 9	ZDHHC9	51114	ENSG00000188706		"Mental retardation, X-linked syndromic, Raymond type, 300799 (3)"	Zdhhc9 (MGI:2444393)			
chrX	129906120	129929761	Xq26.1	Xq26.1		300508	UTP14A	"Utp14, S. cerevisiae, homolog of, A"	UTP14A	10813	ENSG00000156697			Utp14a (MGI:1919804)			
chrX	129980284	130058082	Xq25-q26.1	Xq26.1		300688	BCORL1	BCL6 corepressor-like 1	BCORL1	63035	ENSG00000085185			Bcorl1 (MGI:2443910)			
chrX	130064919	130110712	Xq26	Xq26.1		300775	"ELF4, MEF"	E74-like factor 4	ELF4	2000	ENSG00000102034			Elf4 (MGI:1928377)			
chrX	130129361	130165886	Xq26.1	Xq26.1		300169	"AIFM1, PDCD8, AIF, COXPD6, COWCK, CMTX4, DFNX5"	"Apoptosis-inducing factor, mitochondrion-associated, 1"	AIFM1	9131	ENSG00000156709		"Combined oxidative phosphorylation deficiency 6, 300816 (3), X-linked recessive; Cowchock syndrome, 310490 (3), X-linked recessive; Deafness, X-linked 5, 300614 (3), X-linked recessive"	Aifm1 (MGI:1349419)			
chrX	130110632	130184872	Chr.X	Xq26.1		300333	RAB33A	Ras-associated protein RAB33A	RAB33A	9363	ENSG00000134594			Rab33a (MGI:109493)			
chrX	130339887	130373360	Xq24	Xq26.1		300242	"SLC25A14, BMCP1"	"Solute carrier family 25 (mitochondrial carrier), member 14"	SLC25A14	9016	ENSG00000102078			Slc25a14 (MGI:1330823)			
chrX	130384344	130385536	Xq26.1	Xq26.1		300513	"GPR119, GPCR2"	G protein-coupled receptor 119	GPR119	139760	ENSG00000147262			Gpr119 (MGI:2668412)			
chrX	130622329	130903316	Xq25-q26.2	Xq26.1		300282	ENOX2	ECTO-NOX disulfide-thiol exchanger 2	ENOX2	10495	ENSG00000165675			Enox2 (MGI:2384799)			
chrX	131058241	131089884	Xq26.1	Xq26.1		300937	ARHGAP36	Rho GTPase-activating protein 36	ARHGAP36	158763	ENSG00000147256			Arhgap36 (MGI:1922654)			
chrX	131273505	131289456	Xq25	Xq26.1		300137	"IGSF1, IGDC1, CHTE"	"Immunoglobulin superfamily, member 1"	IGSF1	3547	ENSG00000147255		"Hypothyroidism, central, and testicular enlargement, 300888 (3), X-linked recessive"	Igsf1 (MGI:2147913)			
chrX	131691524	131830642	Xq26.1	Xq26.2		300999	"FIRRE, LINC01200"	Functional intergenic repeating RNA element	FIRRE	286467							
chrX	132023216	132075942	Xq26	Xq26.2		300547	"MASK, MST4"	MST3- and SOK1-related kinase	STK26	51765	ENSG00000134602			Stk26 (MGI:1917665)			
chrX	132074925	132128021	Xq26.2	Xq26.2		300628	"FRMD7, NYS1, XIPAN"	FERM domain-containing 7	FRMD7	90167	ENSG00000165694		"Nystagmus 1, congenital, X-linked, 310700 (3), X-linked; Nystagmus, infantile periodic alternating, X-linked, 310700 (3), X-linked"	Frmd7 (MGI:2686379)			
chrX	132369313	132490029	Xq26	Xq26.2		300413	"MBNL3, MBXL"	Muscleblind-like protein 3	MBNL3	55796	ENSG00000076770			Mbnl3 (MGI:2444912)			
chrX	132626009	132961394	Xq26.2	Xq26.2		300545	HS6ST2	Heparan sulfate 6-O-sulfotransferase 2	HS6ST2	90161	ENSG00000171004			Hs6st2 (MGI:1354959)			
chrX	133024630	133083767	Xq26.2	Xq26.2		300309	USP26	Ubiquitin-specific protease 26	USP26	83844	ENSG00000134588			Usp26 (MGI:1933247)			
chrX	133216668	133218347	Xq26.2	Xq26.2		300772	"TFDP3, HCA661, CT30, DP4"	"Transcription factor DP family, member 3"	TFDP3	51270	ENSG00000183434						
chrX	133301035	133415176	Xq26	Xq26.2		300168	GPC4	Glypican 4	GPC4	2239	ENSG00000076716	centromeric to GPC3		Gpc4 (MGI:104902)			
chrX	133535744	133985645	Xq26	Xq26.2		300037	"GPC3, SDYS, SGBS1"	Glypican 3	GPC3	2719	ENSG00000147257		"Simpson-Golabi-Behmel syndrome, type 1, 312870 (3), X-linked recessive; Wilms tumor, somatic, 194070 (3)"	Gpc3 (MGI:104903)			
chrX	134169670	134169765	Xq26.2	Xq26.2		300722	"MIR19B2, MIRN19B2"	Micro RNA 19B2	MIR19B2	406981							
chrX	134169808	134169876	Xq26.2	Xq26.2		300950	MIR20B	Micro RNA 20B	MIR20B	574032							
chrX	134170197	134170277	Xq26.2	Xq26.2		300792	"MIR106A, MIRN106A"	Micro RNA 106A	MIR106A	406899							
chrX	134373311	134428791	Xq26.3	Xq26.2		300414	"PHF6, BFLS"	PHD finger protein 6	PHF6	84295	ENSG00000156531		"Borjeson-Forssman-Lehmann syndrome, 301900 (3), X-linked recessive"	Phf6 (MGI:1918248)			
chrX	134460144	134500667	Xq26.2	Xq26.2-q26.3		308000	"HPRT1, HPRT"	Hypoxanthine phosphoribosyltransferase 1	HPRT1	3251	ENSG00000165704		"HPRT-related gout, 300323 (3), X-linked recessive; Lesch-Nyhan syndrome, 300322 (3), X-linked recessive"	Hprt (MGI:96217)			
chrX	134500000	138900000	Xq26.3			300795	"CT45A4, CT45.4"	"Cancer/testis antigen family 45, member A4"									
chrX	134500000	138900000	Xq26.3			300942	"CXDUPq26.3, DUPXq26.3, XLAG"	Chromosome Xq26.3 duplication syndrome					"Chromosome Xq26.3 duplication syndrome, 300942 (4), X-linked dominant"				
chrX	134500000	138900000	Xq26.3			300833	SRXX3	46XX sex reversal 3				due to deletion/duplication/rearrangement upstream of SOX3	"46XX sex reversal 3, 300833 (4), X-linked dominant"				
chrX	134546327	134546397	Xq26.3	Xq26.3		300865	MIR503	Micro RNA 503	MIR503	574506							
chrX	134546613	134546710	Xq26.3	Xq26.3		300682	"MIR424, MIRN424, MIR322"	Micro RNA 424	MIR424	494336							
chrX	134565837	134764321	Xq26	Xq26.3		300296	PLAC1	Placenta-specific gene 1	PLAC1	10761	ENSG00000170965			Plac1 (MGI:1926287)			
chrX	134887625	134915343	Xq26.3	Xq26.3		300674	MOSPD1	Motile sperm domain-containing protein 1	MOSPD1	56180	ENSG00000101928			Mospd1 (MGI:1917630)			
chrX	135032302	135033545	Xq26	Xq26.3		300213	CXX1	CAAX box protein 1	RTL8C	8933	ENSG00000134590			Rtl8c (MGI:1920115)			
chrX	135248588	135344628	Xq26	Xq26.3		314997	"ZNF75D, ZNF75"	Zinc finger protein-75D	ZNF75D	7626	ENSG00000186376	1Mb distal to HPRT					
chrX	135344769	135363412	Xq26.3	Xq26.3		300627	"ZNF449, ZSCAN19"	Zinc finger protein 449	ZNF449	203523	ENSG00000173275			Zfp449 (MGI:1925869)			
chrX	135708397	135723317	Xq26.3	Xq26.3		300648	"CT45A1, CT45"	"Cancer/testis antigen family 45, member A1"	CT45A1	541466	ENSG00000268940						
chrX	135760066	135768223	Xq26.3	Xq26.3		300794	"CT45A3, CT45.3"	"Cancer/testis antigen family 45, member A3"	CT45A3	441519	ENSG00000269096						
chrX	135777129	135785513	Xq26.3	Xq26.3		300796	"CT45A5, CT45.5"	"Cancer/testis antigen family 45, member A5"	CT45A5	441521	ENSG00000228836						
chrX	135794686	135802760	Xq26.3	Xq26.3		300797	"CT45A6, CT45.6"	"Cancer/testis antigen family 45, member A6"	CT45A6	541465	ENSG00000278289						
chrX	135811978	135820061	Xq26.3	Xq26.3		300793	"CT45A2, CT45.2"	"Cancer/testis antigen family 45, member A2"	CT45A2	728911	ENSG00000271449						
chrX	135893606	135913060	Xq28	Xq26.3		300359	SAGE	Sarcoma antigen	SAGE1	55511	ENSG00000181433						
chrX	135974595	136047268	Xq26.3	Xq26.3		300231	"SLC9A6, NHE6"	"Solute carrier family 9 (sodium/hydrogen exchanger), member 6"	SLC9A6	10479	ENSG00000198689		"Mental retardation, X-linked syndromic, Christianson type, 300243 (3), X-linked dominant"	Slc9a6 (MGI:2443511)			
chrX	136146701	136211358	Xq27.2	Xq26.3		300163	"FHL1, SLIM1, XMPMA, KYOT, FHL1A, FHL1B, RBMX1A, RBMX1B, FCMSU"	Four-and-a-half LIM domains 1	FHL1	2273	ENSG00000022267	mutation identified in 1 FCMSU family	"Emery-Dreifuss muscular dystrophy 6, X-linked, 300696 (3), X-linked recessive; Myopathy, X-linked, with postural muscle atrophy, 300696 (3), X-linked recessive; Reducing body myopathy, X-linked 1a, severe, infantile or early childhood onset, 300717 (3), X-linked dominant; Reducing body myopathy, X-linked 1b, with late childhood or adult onset, 300718 (3), X-linked; Scapuloperoneal myopathy, X-linked dominant, 300695 (3), X-linked dominant; ?Uruguay faciocardiomusculoskeletal syndrome, 300280 (3), X-linked recessive"	Fhl1 (MGI:1298387)			
chrX	136213219	136256481	Xq26.3	Xq26.3		300930	"MAP7D3, MDP3"	MAP7 domain-containing protein 3	MAP7D3	79649	ENSG00000129680			Map7d3 (MGI:2445051)			
chrX	136487965	136492438	Xq26-q28	Xq26.3		300107	BRS3	Bombesin-like receptor 3	BRS3	680	ENSG00000102239			Brs3 (MGI:1100501)			
chrX	136497078	136512345	Xq26.3	Xq26.3		300346	"HTATSF1, TATSF1"	HIV-1 TAT stimulatory factor 1	HTATSF1	27336	ENSG00000102241			Htatsf1 (MGI:1919709)			
chrX	136532151	136556806	Xq26.1-q27.2	Xq26.3		300583	"VGLL1, VGL1, TDU"	Vestigial-like 1	VGLL1	51442	ENSG00000102243			Vgll1 (MGI:2655768)			
chrX	136648176	136660389	Xq26	Xq26.3		300386	"TNFSF5, CD40LG, HIGM1, IGM"	"Tumor necrosis factor ligand superfamily, member 5"	CD40LG	959	ENSG00000102245	Between DSX144E and DSX300	"Immunodeficiency, X-linked, with hyper-IgM, 308230 (3), X-linked recessive"	Cd40lg (MGI:88337)			
chrX	136665546	136781343	Xq26	Xq26.3		300267	"ARHGEF6, MRX46, COOL2"	Rho guanine nucleotide exchange factor-6	ARHGEF6	9459	ENSG00000129675		"Mental retardation, X-linked 46, 300436 (3), X-linked recessive"	Arhgef6 (MGI:1920591)			
chrX	136869193	136880779	Xq26	Xq26.3		300199	"RBMX, MRXS11"	"RNA-binding motif protein, X chromosome"	RBMX	27316	ENSG00000147274	mutation identified in 1 MRXS11 family	"?Mental retardation, X-linked, syndromic 11, Shashi type, 300238 (3), X-linked recessive"	Rbmx (MGI:1343044)			
chrX	137030147	137031673	Xq26.3	Xq26.3		300393	"GPR101, PAGH2, PITA2"	G protein-coupled receptor 101	GPR101	83550	ENSG00000165370		"Pituitary adenoma 2, GH-secreting, 300943 (3)"	Gpr101 (MGI:2685211)			
chrX	137566126	137577690	Xq26.2	Xq26.3		300265	"ZIC3, HTX1, HTX, VACTERLX"	"Zic family, member 3"	ZIC3	7547	ENSG00000156925		"Congenital heart defects, nonsyndromic, 1, X-linked, 306955 (3), X-linked recessive; Heterotaxy, visceral, 1, X-linked, 306955 (3), X-linked recessive; VACTERL association, X-linked, 314390 (3), X-linked recessive"	Zic3 (MGI:106676)			
chrX	138631572	139222888	Xq26.3	Xq26.3-q27.1		300070	"FGF13, FGF2"	Fibroblast growth factor-13	FGF13	2258	ENSG00000129682			Fgf13 (MGI:109178)			
chrX	138900000	148000000	Xq27			300536	BMND4	Bone mineral density QTL 4		554316			"[Bone mineral density QTL 4], 300536 (2)"				
chrX	138900000	141200000	Xq27.1			300898	"CIRS7, CDR1AS"	Circular RNA sponge for MIR7									
chrX	138900000	148000000	Xq27			300085	COD2	"Cone dystrophy-2, X-linked"	COD2	1275			"Cone dystrophy, progressive X-linked, 2, 300085 (2), X-linked"				
chrX	138900000	156040895	Xq27-q28			300147	HPCX1	"Prostate cancer, hereditary, X-linked 1"	HPCX	9566		between D3S2390 and bG82i1.0	"{Prostate cancer, hereditary, X-linked 1}, 300147 (2)"				
chrX	138900000	141200000	Xq27.1			307150	"HTC2, HCG, CGH, CXINSq27.1"	"Hypertrichosis, congenital generalized"				palindrome-mediated interchromosomal insertion at Xq27.1	"Hypertrichosis, congenital generalized, 307150 (4), X-linked dominant"				
chrX	138900000	156040895	Xq27-q28			301590	"MCOPS4, ANOP1"	"Microphthalmia, syndromic 4"	ANOP1	289			"?Microphthalmia, syndromic 4, 301590 (2), X-linked recessive"				
chrX	138900000	148000000	Xq27			300228	TGCT1	Testicular germ cell tumor 1	TGCT1	50830			"Testicular germ cell tumor, 300228 (2)"				
chrX	139530719	139563458	Xq27.1-q27.2	Xq27.1		300746	"F9, HEMB, THPH8"	Coagulation factor IX (plasma thromboplastic component)	F9	2158	ENSG00000101981	distal to HPRT; proximal part of Xq27	"{Deep venous thrombosis, protection against}, 300807 (3); Hemophilia B, 306900 (3), X-linked recessive; Thrombophilia, X-linked, due to factor IX defect, 300807 (3); {Warfarin sensitivity}, 122700 (3), Autosomal dominant"	F9 (MGI:88384)			
chrX	139581767	139708278	Xq27	Xq27.1		311030	"MCF2, DBL"	Oncogene MCF2 (oncogene DBL)	MCF2	4168	ENSG00000101977	~60kb telomeric to F9; 5' replacement by chr.15 segment		Mcf2 (MGI:96932)			
chrX	139726345	139933082	Xq27	Xq27.1		300516	"ATP11C, ATPIQ, ATPIG"	"ATPase, class VI, type 11C"	ATP11C	286410	ENSG00000101974			Atp11c (MGI:1859661)			
chrX	140502986	140505059	Xq26.3	Xq27.1		313430	"SOX3, MRGH"	SRY (sex determining region Y)-box 3	SOX3	6658	ENSG00000134595	P mutant in BFLS	"Mental retardation, X-linked, with isolated growth hormone deficiency, 300123 (3); Panhypopituitarism, X-linked, 312000 (3), X-linked"	Sox3 (MGI:98365)			
chrX	140783259	140784557	Xq27.1-q27.2	Xq27.1		302650	"CDR1, CDR62A"	"Cerebellar degeneration-related protein-1, 34kD"	CDR1	1038	ENSG00000184258	between HPRT and F9					
chrX	141002590	141003705	Xq27.1-q27.3	Xq27.1		300669	"SPANXB1, SPANXB"	"SPANX family, member B1"	SPANXB1	728695	ENSG00000227234						
chrX	141175744	141177213	Xq27	Xq27.1		300402	LDOC1	Leucine zipper downregulated in cancer 1	LDOC1	23641	ENSG00000182195			Ldoc1 (MGI:2685212)			
chrX	141200000	156040895	Xq27.2-q28			300388	"BPP, PMGX, CBPS"	"Polymicrogyria, bilateral perisylvian"				possible genetic heterogeneity	"Polymicrogyria, bilateral perisylvian, 300388 (2), X-linked dominant"				
chrX	141241462	141242549	Xq26.3-q27.1	Xq27.2		300330	"SPANXC, CTP11"	"Sperm protein associated with the nucleus, X chromosome, family member C"	SPANXC	64663	ENSG00000198573						
chrX	141583673	141584737	Xq27.1	Xq27.2		300305	"SPANXA1, SPANX"	"Sperm protein associated with the nucleus, X chromosome, family member A1"	SPANXA1	30014	ENSG00000198021						
chrX	141589707	141590771	Xq27.2	Xq27.2		300493	SPANXA2	"Sperm protein associated with the nucleus, X chromosome, family member A2"	SPANXA2	728712	ENSG00000203926						
chrX	141697400	141698738	Xq27.1	Xq27.2		300670	SPANXD	"SPANX family, member D"	SPANXD	64648	ENSG00000196406						
chrX	141697400	141698738	Xq27.1	Xq27.2		300671	SPANXE	"SPANX family, member E"	SPANXD	64648	ENSG00000196406						
chrX	141838315	141898141	Xq27	Xq27.2		300469	MAGEC3	"Melanoma antigen, family C, 3"	MAGEC3	139081	ENSG00000165509						
chrX	141903855	141909400	Xq26	Xq27.2		300223	MAGEC1	"Melanoma antigen, family C, 1"	MAGEC1	9947	ENSG00000155495						
chrX	142202341	142205289	Xq27	Xq27.2		300468	"MAGEC2, MAGEE1, CT10, HCA587"	"Melanoma antigen, family C, 2"	MAGEC2	51438	ENSG00000046774						
chrX	143000000	156040895	Xq27.3-q28			300869	"DUPXq27.3q28, CXDUPq27.3q28"	Chromosome Xq27.3-q28 duplication syndrome					"Chromosome Xq27.3-q28 duplication syndrome, 300869 (4), X-linked recessive"				
chrX	143000000	148000000	Xq27.3			300509	DYX9	"Dyslexia, susceptibility to, 9"	DYX9	474159		max lod at DXS8043	"{Dyslexia, susceptibility to, 9}, 300509 (2)"				
chrX	143000000	156040895	Xq27.3-qter			302000	EBM	"Epidermolysis bullosa, macular type"	EBM	1881							
chrX	143025917	143038636	Xq27	Xq27.3		300667	SPANXN4	"SPANX family, member N4"	SPANXN4	441525	ENSG00000189326						
chrX	143508734	143517474	Xq27	Xq27.3		300666	SPANXN3	"SPANX family, member N3"	SPANXN3	139067	ENSG00000189252						
chrX	143622789	143636106	Xq27	Xq27.3		300562	SLITRK4	"SLIT- and NTRK-like family, member 4"	SLITRK4	139065	ENSG00000179542			Slitrk4 (MGI:2442509)			
chrX	143712034	143720667	Xq27	Xq27.3		300665	SPANXN2	"SPANX family, member N2"	SPANXN2	494119	ENSG00000268988						
chrX	145247586	145256207	Xq27	Xq27.3		300664	SPANXN1	"SPANX family, member N1"	SPANXN1	494118	ENSG00000203923						
chrX	145817828	145829855	Xq27	Xq27.3		300561	"SLITRK2, KIAA1854, CXorf1, CXorf2"	"SLIT- and NTRK-like family, member 2"	SLITRK2	84631	ENSG00000185985			Slitrk2 (MGI:2679449)			
chrX	147230719	147230842	Xq27.3	Xq27.3		300877	MIR506	Micro RNA 506	MIR506	574511							
chrX	147236912	147237026	Xq27.3	Xq27.3		300874	MIR508	Micro RNA 508	MIR508	574513							
chrX	147259651	147259725	Xq27.3	Xq27.3		300876	MIR509-3	Micro RNA 509-3	MIR509-3	100126337							
chrX	147260531	147260624	Xq27.3	Xq27.3		300875	MIR509-1	Micro RNA 509-2	MIR509-1	574514							
chrX	147272334	147272407	Xq27.3	Xq27.3		300866	MIR510	Micro RNA 510	MIR510	574515							
chrX	147909430	147911816	Xq27	Xq27.3		300805	"FMR1AS1, ASFMR1"	FMR1 antisense RNA 1	FMR1-AS1	100126270							
chrX	147911950	147951126	Xq27.3	Xq27.3		309550	"FMR1, FRAXA, POF1"	FMR1 gene	FMR1	2332	ENSG00000102081	8-8.7Mb from telomere	"Fragile X syndrome, 300624 (3), X-linked dominant; Fragile X tremor/ataxia syndrome, 300623 (3), X-linked dominant; Premature ovarian failure 1, 311360 (3), X-linked"	Fmr1 (MGI:95564)			
chrX	148000000	156040895	Xq28			300843	BED	Bornholm eye disease		100653365		linked to F8	"Bornholm eye disease, 300843 (2), X-linked recessive"				
chrX	148000000	156040895	Xq28			300815	"DUPXq28, CXq28"	Chromosome Xq28 duplication syndrome					"Chromosome Xq28 duplication syndrome, 300815 (4)"				
chrX	148000000	156040895	Xq28			305424	"DXS522E, F8B"	"DNA segment, single copy, expressed probes, intron 22 probe, F8B"									
chrX	148000000	156040895	Xq28			306995	"HMS1, GAY1"	"Homosexuality, male"					"[?Homosexuality, male], 306995 (2), X-linked"				
chrX	148000000	156040895	Xq28			309200	"MAFD2, MDX"	Major affective disorder 2	MAFD2	4096		"linkage to G6PD,CB in non-Ashkenazi Jews"	"{?Major affective disorder 2}, 309200 (2), X-linked dominant"				
chrX	148000000	156040895	Xq28			309620	"MRSD, CHRS"	Mental retardation-skeletal dysplasia	MRSD	4364			"Mental retardation-skeletal dysplasia, 309620 (2), X-linked"				
chrX	148000000	156040895	Xq28			300261	MRXSA	Armfield X-linked mental retardation syndrome		57791			"Mental retardation syndrome, X-linked, Armfield type, 300261 (2), X-linked recessive"				
chrX	148000000	156040895	Xq28			300845	"MYMY4, CXDELq38"	"Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism and facial dysmorphism"				contiguous gene deletion syndrome (3.4kb)	"Moyamoya disease 4, 300845 (4), X-linked recessive"				
chrX	148000000	156040895	Xq28			310460	MYP1	"Myopia 1, X-linked"	MYP1	4657			"Myopia-1, 310460 (2), X-linked recessive"				
chrX	148000000	156040895	Xq28			300605	RP34	Retinitis pigmentosa 34	RP34	777642			"Retinitis pigmentosa 34, 300605 (2)"				
chrX	148000000	156040895	Xq28			300809	SLEB15	"Systemic lupus erythematosus, susceptibility to, 15"		100379200		associated with rs17435	"{Systemic lupus erythematosus, susceptibility to, 15}, 300809 (2)"				
chrX	148000000	156040895	Xq28			314300	"TKCR, TKC"	"Torticollis, keloids, cryptorchidism and renal dysplasia"	TKCR	7085		distal to G6PD	"Goeminne TKCR syndrome, 314300 (2), X-linked"				
chrX	148000000	156040895	Xq28			314900	XM	Xm	XM	7506		"linked to DCB, PCB"					
chrX	148500618	149000662	Xq28	Xq28		300806	"AFF2, FMR2, FRAXE, MRX2"	"AF4/FMR2 family, member 2 (fragile site, X-linked, E)"	AFF2	2334	ENSG00000155966		"Mental retardation, X-linked, FRAXE type, 309548 (3), X-linked recessive"				
chrX	149476989	149505353	Xq28	Xq28		300823	"IDS, MPS2, SIDS"	Iduronate 2-sulfatase (Hunter syndrome)	IDS	3423	ENSG00000010404	telomeric IDS2 source of inversion in IDS	"Mucopolysaccharidosis II, 309900 (3), X-linked recessive"	Ids (MGI:96417)			
chrX	149540629	149555344	Xq27	Xq28		300954	"CXorf40A, EOLA1"	Chromosome X open reading frame 40A	CXorf40A	91966	ENSG00000197620			1110012L19Rik (MGI:1915868)			
chrX	149581652	149587467	Xq28	Xq28		300764	MAGEA9B	"Melanoma antigen, family A, 9B"	MAGEA9B	728269	ENSG00000267978						
chrX	149596555	149631911	Xq28	Xq28		300031	"FAM11A, FRAXF"	"Family with sequence similarity 11, member A"	TMEM185A	84548	ENSG00000269556			Tmem185a (MGI:2448555)			
chrX	149688201	149717267	Xq28	Xq28		300344	"MAGEA11, MAGE11"	"Melanoma antigen, family A, 11"	MAGEA11	4110	ENSG00000185247			Magea4 (MGI:1333839)			
chrX	149781875	149787736	Xq28	Xq28		300342	"MAGEA9, MAGE9"	"Melanoma antigen, family A, 9"	MAGEA9	4108	ENSG00000123584						
chrX	149825707	149879798	Xq28	Xq28		300892	"LINC00850, KUCG1"	Long intergenic noncoding RNA 850	LINC00850	101241891							
chrX	149881140	149885834	Xq28	Xq28		300341	"MAGEA8, MAGE8"	"Melanoma antigen, family A, 8"	MAGEA8	4107	ENSG00000156009						
chrX	150361563	150514177	Xq28	Xq28		300120	"MAMLD1, CXorf6, F18, HYSP2"	Mastermind-like domain containing 1	MAMLD1	10046	ENSG00000013619	near MTM1 in microdeletion	"Hypospadias 2, X-linked, 300758 (3), X-linked recessive"				
chrX	150562657	150673142	Xq28	Xq28		300415	"MTM1, MTMX"	Myotubularin	MTM1	4534	ENSG00000171100	close to F8	"Myotubular myopathy, X-linked, 310400 (3), X-linked recessive"	Mtm1 (MGI:1099452)			
chrX	150692961	150765102	Xq28	Xq28		300171	MTMR1	Myotubularin-related protein-1	MTMR1	8776	ENSG00000063601			Mtmr1 (MGI:1858271)			
chrX	150766335	150898815	Xq28	Xq28		300846	"CD99L2, CD99B"	CD99 antigen-like 2	CD99L2	83692	ENSG00000102181			Cd99l2 (MGI:2177151)			
chrX	150980507	150990774	Xq28	Xq28		300193	"HMGB3, HMG4, HMG2A, MCOPS13"	High-mobility group box 3 (high mobility group protein 4)	HMGB3	3149	ENSG00000029993	mutation identified in 1 MCOPS13 family	"?Microphthalmia, syndromic 13, 300915 (3), X-linked"				
chrX	151176583	151182854	Xq28	Xq28		300207	GPR50	G protein-coupled receptor 50	GPR50	9248	ENSG00000102195			Gpr50 (MGI:1333877)			
chrX	151396554	151409363	Xq28	Xq28		300913	"VMA21, XMEA"	"Vma21, S. cerevisiae, homolog of"	VMA21	203547	ENSG00000160131		"Myopathy, X-linked, with excessive autophagy, 310440 (3), X-linked recessive"				
chrX	151563183	151676738	Xq28	Xq28		300993	"PASD1, CT64, OXTES1"	PAS domain-containing repressor 1	PASD1	139135	ENSG00000166049						
chrX	151694605	151701590	Xq28	Xq28		300685	"PRRG3, PRGP3, TMG3"	Proline-rich gamma-carboxyglutamic acid protein 3	PRRG3	79057	ENSG00000130032			Prrg3 (MGI:2685214)			
chrX	151716035	151723193	Xq28	Xq28		300450	FATE1	Fetal and adult testis-expressed gene 1	FATE1	89885	ENSG00000147378						
chrX	151734745	151745563	Xq27	Xq28		300338	"CNGA2, CNG2, OCNC1"	"Cyclic nucleotide-gated channel, alpha-2"	CNGA2	1260	ENSG00000183862			Cnga2 (MGI:108040)			
chrX	151912888	151925169	Xq28	Xq28		300175	"MAGEA4, MAGE4A, MAGE4B"	"Melanoma antigen, family A, 4"	MAGEA4	4103	ENSG00000147381						
chrX	151953123	151974691	Xq28	Xq28		300093	GABRE	"Gamma-aminobutyric acid (GABA) A receptor, epsilon"	GABRE	2564	ENSG00000102287						
chrX	151958577	151958657	Xq28	Xq28		300769	"MIR224, MIRN224"	Micro RNA 224	MIR224	407009							
chrX	152114048	152117938	Xq28	Xq28		300340	"MAGEA5, MAGE5"	"Melanoma antigen, family A, 5"	MAGEA5	4104							
chrX	152133309	152138577	Xq28	Xq28		300343	"MAGEA10, MAGE10"	"Melanoma antigen, family A, 10"	MAGEA10	4109	ENSG00000124260			Magea10 (MGI:3588211)			
chrX	152166233	152451358	Xq28	Xq28		305660	GABRA3	"Gamma-aminobutyric acid (GABA) A receptor, alpha-3"	GABRA3	2556	ENSG00000011677	4Mb from telomere		Gabra3 (MGI:95615)			
chrX	152392218	152392298	Xq28	Xq28		300811	"MIR105-1, MIRN105-1"	Micro RNA 105-1	MIR105-1	406897							
chrX	152394411	152394491	Xq28	Xq28		300812	"MIR105-2, MIRN105-2"	Micro RNA 105-2	MIR105-2	406898							
chrX	152637894	152659827	Xq28	Xq28		300349	GABRQ	"Gamma-aminobutyric acid receptor, theta"	GABRQ	55879	ENSG00000268089			Gabrq (MGI:1888498)			
chrX	152698741	152702346	Xq28	Xq28		300174	"MAGEA3, MAGE3"	"Melanoma antigen, family A, 3"	MAGEA3	4102	ENSG00000221867						
chrX	152714527	152718606	Xq28	Xq28		300549	MAGEA2B	"Melanoma antigen, family A, 2B"	MAGEA2B	266740	ENSG00000183305						
chrX	152727483	152733735	Xq28	Xq28		300944	"CSAG1, CSAGE"	"CSAG family, member 1 `"	CSAG1	158511	ENSG00000198930						
chrX	152733778	152737668	Xq28	Xq28		300177	"MAGEA12, MAGE12"	"Melanoma antigen, family A, 12"	MAGEA12	4111	ENSG00000213401						
chrX	152749862	152753941	Xq28	Xq28		300173	"MAGEA2, MAGE2"	"Melanoma antigen, family A, 2"	MAGEA2	4101	ENSG00000268606						
chrX	152766135	152769728	Xq28	Xq28		300176	"MAGEA6, MAGE6"	"Melanoma antigen, family A, 6"	MAGEA6	4105	ENSG00000197172						
chrX	152827326	152830756	Xq28	Xq28		300006	"CETN2, CALT"	"Centrin, EF-hand protein, 2 (caltractin)"	CETN2	1069	ENSG00000147400			Cetn2 (MGI:1347085)			
chrX	152830966	152869362	Xq28	Xq28		300275	NSDHL	NAD(P)H steroid dehydrogenase-like protein	NSDHL	50814	ENSG00000147383		"CHILD syndrome, 308050 (3), X-linked dominant; CK syndrome, 300831 (3), X-linked recessive"	Nsdhl (MGI:1099438)			
chrX	152898131	152973480	Xq28	Xq28		300381	ZNF185	Zinc finger protein 185	ZNF185	7739	ENSG00000147394						
chrX	152988823	152994457	Xq28	Xq28		300916	"PNMA5, KIAA1934"	"Paraneoplastic MA antigen family, member 5"	PNMA5	114824	ENSG00000198883			Pnma5 (MGI:2180566)			
chrX	153056408	153060466	Xq28	Xq28		300675	"PNMA3, MA3"	Paraneoplastic MA antigen 3	PNMA3	29944	ENSG00000183837			Pnma3 (MGI:2180565)			
chrX	153072413	153075018	Xq28	Xq28		300917	"PNMA6A, PNMA6"	"Paraneoplastic MA antigen family, member 6A"	PNMA6A	84968	ENSG00000235961						
chrX	153179283	153183877	Xq28	Xq28		300016	MAGE1	Melanoma antigen 1 (directs expression of antigen MZ2-E)	MAGEA1	4100	ENSG00000198681	cluster of 12 genes					
chrX	153444719	153446486	Xq28	Xq28		300370	TREX2	3-prime repair exonuclease 2	TREX2	11219	ENSG00000183479			Trex2 (MGI:1346343)			
chrX	153447664	153495524	Xq28	Xq28		300540	"HAUS7, UCHL5IP, UIP1"	"HAUS augmin-like complex, subunit 7"	HAUS7	55559	ENSG00000213397			Haus7 (MGI:1920988)			
chrX	153494888	153509553	Xq28	Xq28		301870	"BGN, SEMDX, MRLS"	Biglycan	BGN	633	ENSG00000182492	proximal Xq28	"Meester-Loeys syndrome, 300989 (3), X-linked; Spondyloepimetaphyseal dysplasia, X-linked, 300106 (3), X-linked recessive"	Bgn (MGI:88158)			
chrX	153517676	153582928	Xq28	Xq28		300014	"ATP2B3, PMCA3, SCAX1"	"ATPase, Ca++ transporting, plasma membrane, 3"	ATP2B3	492	ENSG00000067842	mutation identified in 1 family	"?Spinocerebellar ataxia, X-linked 1, 302500 (3), X-linked recessive"	Atp2b3 (MGI:1347353)			
chrX	153587924	153599176	Xq28	Xq28		300708	"FAM58A, STAR"	"Family with sequence similarity 58, member A"	CCNQ	92002	ENSG00000262919		"STAR syndrome, 300707 (3), X-linked dominant"	Fam58b (MGI:1916359)			
chrX	153642442	153651325	Xq28	Xq28		300134	"DUSP9, MKP4"	Dual-specificity phosphatase 9	DUSP9	1852	ENSG00000130829			Dusp9 (MGI:2387107)			
chrX	153669722	153687567	Xq28	Xq28		300680	"PNCK, CAMK1B, BSTK3"	"Pregnancy-upregulated, nonubiquitous, CAM kinase"	PNCK	139728	ENSG00000130822			Pnck (MGI:1347357)			
chrX	153688296	153696592	Xq28	Xq28		300036	"SLC6A8, CRTR, CCDS1"	"Solute carrier family 6 (neurotransmitter transporter, creatine), member 8"	SLC6A8	6535	ENSG00000130821	distal to G6PD	"Cerebral creatine deficiency syndrome 1, 300352 (3), X-linked recessive"	Slc6a8 (MGI:2147834)			
chrX	153700491	153724745	Xq28	Xq28		300398	"BCAP31, BAP31, DXS1357E, DDCH"	B-cell receptor-associated protein 31	BCAP31	10134	ENSG00000185825		"Deafness, dystonia, and cerebral hypomyelination, 300475 (3), X-linked recessive"	Bcap31 (MGI:1350933)			
chrX	153724850	153744761	Xq28	Xq28		300371	"ABCD1, ALD, AMN"	"ATP-binding cassette, subfamily D, member 1"	ABCD1	215	ENSG00000101986	about 650kb from GCP/RCP	"Adrenoleukodystrophy, 300100 (3), X-linked recessive; Adrenomyeloneuropathy, adult, 300100 (3), X-linked recessive"	Abcd1 (MGI:1349215)			
chrX	153764195	153779345	Xq28	Xq28		300214	"PLXNB3, PLXN6"	Plexin B3	PLXNB3	5365	ENSG00000198753			Plxnb3 (MGI:2154240)			
chrX	153781000	153785731	Xq28	Xq28		301002	"SRPK3, STK23, MSSK1"	"Protein kinase, serine/arginine-specific, 3"	SRPK3	26576	ENSG00000184343			Srpk3 (MGI:1891338)			
chrX	153785765	153794522	Xq28	Xq28		300089	IDH3G	"Isocitrate dehydrogenase 3 (NAD+), gamma"	IDH3G	3421	ENSG00000067829			Idh3g (MGI:1099463)			
chrX	153794174	153798511	Xq28	Xq28		300090	"SSR4, TRAPD, CDG1Y"	"Signal sequence receptor, delta"	SSR4	6748	ENSG00000180879		"Congenital disorder of glycosylation, type Iy, 300934 (3), X-linked recessive"	Ssr4 (MGI:1099464)			
chrX	153802165	153830566	Xq28	Xq28		300634	"PDZD4, PDZK4, PDZRN4L, KIAA1444, LU1"	PDZ domain-containing 4	PDZD4	57595	ENSG00000067840			Pdzd4 (MGI:2443483)			
chrX	153861513	153886173	Xq28	Xq28		308840	"L1CAM, CAML1, HSAS1, MASA, SPG1"	L1 cell adhesion molecule	L1CAM	3897	ENSG00000198910	between RCP/GCP cluster and G6PD	"CRASH syndrome, 303350 (3), X-linked recessive; Corpus callosum, partial agenesis of, 304100 (3), X-linked recessive; Hydrocephalus due to aqueductal stenosis, 307000 (3), X-linked recessive; Hydrocephalus with Hirschsprung disease, 307000 (3), X-linked recessive; Hydrocephalus with congenital idiopathic intestinal pseudoobstruction, 307000 (3), X-linked recessive; MASA syndrome, 303350 (3), X-linked recessive"	L1cam (MGI:96721)			
chrX	153902530	153907165	Xq28	Xq28		300538	"AVPR2, DIR, DI1, ADHR"	Arginine vasopressin receptor-2	AVPR2	554	ENSG00000126895		"Diabetes insipidus, nephrogenic, 304800 (3), X-linked recessive; Nephrogenic syndrome of inappropriate antidiuresis, 300539 (3), X-linked recessive"	Avpr2 (MGI:88123)			
chrX	153907375	153926259	Xq28	Xq28		300023	RGC1	Rho-GAP hematopoietic protein C1	ARHGAP4	393	ENSG00000089820			Arhgap4 (MGI:2159577)			
chrX	153929826	153935153	Xq28	Xq28		300013	"NAA10, ARD1A, ARD1, TE2, NATD, OGDNS, MCOPS1"	"N-alpha-acetyltransferase 10, NatA catalytic subunit"	NAA10	8260	ENSG00000102030	mutation identified in 1 MCOPS1 family	"?Microphthalmia, syndromic 1, 309800 (3), X-linked; Ogden syndrome, 300855 (3), X-linked recessive, X-linked dominant"	Naa10 (MGI:1915255)			
chrX	153935262	153944779	Xq28	Xq28		312420	RENBP	Renin-binding protein	RENBP	5973	ENSG00000102032			Renbp (MGI:105940)			
chrX	153947555	153972359	Xq28	Xq28		300019	"HCFC1, HCF1, MRX3"	Host cell factor C1 (VP16-accessory protein)	HCFC1	3054	ENSG00000172534	50kb distal to V2R	"Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ), 309541 (3), X-linked recessive"	Hcfc1 (MGI:105942)			
chrX	153972539	153983194	Xq28	Xq28		300059	"TMEM187, CXorf12, DXS9878E, ITBA1 gene"	Transmembrane protein 187	TMEM187	8269	ENSG00000177854						
chrX	154010505	154019983	Xq28	Xq28		300283	IRAK1	Interleukin 1 receptor-associated kinase 1	IRAK1	3654	ENSG00000184216			Irak1 (MGI:107420)			
chrX	154019919	154019988	Xq28	Xq28		300929	MIR718	Micro RNA 718	MIR718	100313781							
chrX	154021799	154097730	Xq28	Xq28		300005	"MECP2, RTT, PPMX, MRX16, MRX79, AUTSX3, MRXSL, MRXS13"	Methyl-CpG-binding protein-2	MECP2	4204	ENSG00000169057	70kb centromeric of RCP/GCP	"{Autism susceptibility, X-linked 3}, 300496 (3), Isolated cases, X-linked, Multifactorial; Encephalopathy, neonatal severe, 300673 (3), X-linked recessive; Mental retardation, X-linked syndromic, Lubs type, 300260 (3), X-linked recessive; Mental retardation, X-linked, syndromic 13, 300055 (3), X-linked recessive; Rett syndrome, 312750 (3), X-linked dominant; Rett syndrome, atypical, 312750 (3), X-linked dominant; Rett syndrome, preserved speech variant, 312750 (3), X-linked dominant"	Mecp2 (MGI:99918)			
chrX	154137726	154144285	Xq28	Xq28		300824	OPN1C	"OPN1LW and OPN1MW genes, controller of"		107604627							
chrX	154144223	154159031	Xq28	Xq28		300822	"OPN1LW, RCP, CBP, CBBM"	"Red cone pigment (opsin 1, long-wave-sensitive)"	OPN1LW	5956	ENSG00000102076	5' to CBD	"Blue cone monochromacy, 303700 (3), X-linked recessive; Colorblindness, protan, 303900 (3), X-linked"	Opn1mw (MGI:1097692)			
chrX	154182595	154196860	Xq28	Xq28		300821	"OPN1MW, GCP, CBD, CBBM"	"Green cone pigment (opsin 1, medium-wave-sensitive)"	OPN1MW	2652	ENSG00000268221	linked to G6PD; multiple genes	"Blue cone monochromacy, 303700 (3), X-linked recessive; Colorblindness, deutan, 303800 (3), X-linked"				
chrX	154271264	154295355	Xq28	Xq28		300092	TEX28	Testis-expressed gene on Xq28	TEX28	1527	ENSG00000278057			Tex28 (MGI:2686384)			
chrX	154295673	154330362	Xq28	Xq28		300044	"TKTL1, TKT2, TKR"	Transketolase-like 1	TKTL1	8277	ENSG00000007350	between GCP and FLN1		Tktl1 (MGI:1933244)			
chrX	154348531	154374637	Xq28	Xq28		300017	"FLNA, FLN1, NHBP, OPD1, OPD2, FMD, MNS, CVD1, CSBS, FGS2"	"Filamin A, alpha (actin-binding protein-280)"	FLNA	2316	ENSG00000196924	mutation identified in 1 FGS2 patient	"Cardiac valvular dysplasia, X-linked, 314400 (3), X-linked recessive; Congenital short bowel syndrome, 300048 (3), X-linked recessive; ?FG syndrome 2, 300321 (3), X-linked; Frontometaphyseal dysplasia 1, 305620 (3), X-linked recessive; Heterotopia, periventricular, 300049 (3), X-linked dominant; Intestinal pseudoobstruction, neuronal, 300048 (3), X-linked recessive; Melnick-Needles syndrome, 309350 (3), X-linked dominant; Otopalatodigital syndrome, type I, 311300 (3), X-linked dominant; Otopalatodigital syndrome, type II, 304120 (3), X-linked dominant; Terminal osseous dysplasia, 300244 (3), X-linked dominant"	Flna (MGI:95556)			
chrX	154379235	154381522	Xq28	Xq28		300384	"EMD, EDMD, STA"	Emerin	EMD	2010	ENSG00000102119	in distal Xq28	"Emery-Dreifuss muscular dystrophy 1, X-linked, 310300 (3), X-linked recessive"	Emd (MGI:108117)			
chrX	154398064	154402338	Xq28	Xq28		312173	"RPL10, DXS648, QM, AUTSX5, MRXS35"	Ribosomal protein L10	RPL10	6134	ENSG00000147403		"{Autism, susceptibility to, X-linked 5}, 300847 (3); Mental retardation, X-linked, syndromic, 35, 300998 (3), X-linked recessive"	Rpl10 (MGI:105943)			
chrX	154401235	154412100	Xq28	Xq28		300081	"DNASE1L1, DNL1L"	Deoxyribonuclease I-like 1	DNASE1L1	1774	ENSG00000013563	between QM and DXS1010E		Dnase1l1 (MGI:109628)			
chrX	154411517	154421725	Xq28	Xq28		300394	"TAZ, EFE2, BTHS, CMD3A, LVNCX"	Tafazzin	TAZ	6901	ENSG00000102125		"Barth syndrome, 302060 (3), X-linked recessive"	Taz (MGI:109626)			
chrX	154428631	154436516	Xq28	Xq28		300197	"ATP6AP1, ATP6IP1, ATP6S1, VATPS1"	"ATPase, H+ transporting, lysosomal, accessory protein 1"	ATP6AP1	537	ENSG00000071553		"Immunodeficiency 47, 300972 (3), X-linked recessive"	Atp6ap1 (MGI:109629)			
chrX	154436912	154443466	Xq28	Xq28		300104	"GDI1, RABGD1A, MRX41, MRX48"	GDP dissociation inhibitor 1	GDI1	2664	ENSG00000203879		"Mental retardation, X-linked 41, 300849 (3), X-linked dominant"	Gdi1 (MGI:99846)			
chrX	154444125	154450653	Xq28	Xq28		300453	"FAM50A, DXS9928E, HXC26"	"Family with sequence similarity 50, member A"	FAM50A	9130	ENSG00000071859			Fam50a (MGI:1351626)			
chrX	154458280	154473645	Xq28	Xq28		300022	SEX	Sex chromosome X transmembrane protein of HGF receptor family 3	PLXNA3	55558	ENSG00000130827			Plxna3 (MGI:107683)			
chrX	154477768	154479256	Xq28	Xq28		300060	"LAGE3, ITBA2, GAMOS2"	L antigen family member 3	LAGE3	8270	ENSG00000196976		"Galloway-Mowat syndrome 2, X-linked, 301006 (3), X-linked recessive"				
chrX	154483716	154486669	Xq28	Xq28		312070	"UBL4A, GDX, UBL4, DX254E"	Ubiquitin-like 4A	UBL4A	8266	ENSG00000102178	40kb 3' to G6PD		"Ubl4a,Gm44504 (MGI:95049,MGI:5621304)"			
chrX	154487305	154490689	Xq28	Xq28		312090	"SLC10A3, P3"	Solute carrier family 10 (sodium/bile acid cotransporter family) member 3 (protein p3)	SLC10A3	8273	ENSG00000126903	order: G6PD-3'-(7kb)-5'-P3-3'-(0.5kb)-5'-GDX		Slc10a3 (MGI:95048)			
chrX	154506158	154516256	Xq28	Xq28		300492	FAM3A	"Family with sequence similarity 3, member A"	FAM3A	60343	ENSG00000071889			Fam3a (MGI:1913544)			
chrX	154531389	154547585	Xq28	Xq28		305900	"G6PD, G6PD1"	Glucose-6-phosphate dehydrogenase	G6PD	2539	ENSG00000160211		"Hemolytic anemia, G6PD deficient (favism), 300908 (3), X-linked dominant; {Resistance to malaria due to G6PD deficiency}, 611162 (3)"	G6pdx (MGI:105979)			
chrX	154542239	154565045	Xq28	Xq28		300248	"IKBKG, NEMO, FIP3, IP, IPD2, AMCBX1, IMD33"	"Inhibitor of kappa light polypeptide gene enhancer in B cells, kinase of, gamma (NF-kappa-B essential modulator)"	IKBKG	8517	ENSG00000269335		"Ectodermal dysplasia, hypohidrotic, with immune deficiency, 300291 (3); Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301 (3); Immunodeficiency 33, 300636 (3), X-linked recessive; Immunodeficiency, isolated, 300584 (3); Incontinentia pigmenti, 308300 (3), X-linked dominant; Invasive pneumococcal disease, recurrent isolated, 2, 300640 (3)"	Ikbkg (MGI:1338074)			
chrX	154585153	154586815	Xq28	Xq28		300657	"CTAG1A, LAGE2A"	Cancer/testis antigen 1A	CTAG1A	246100	ENSG00000268651						
chrX	154617608	154619270	Xq28	Xq28		300156	"CTAG1B, CTAG1"	Cancer/testis antigen 1B	CTAG1B	1485	ENSG00000184033						
chrX	154651971	154653578	Xq28	Xq28		300396	"CTAG2, LAGE1, CAMEL"	Cancer/testis antigen 2	CTAG2	30848	ENSG00000126890						
chrX	154675248	154751582	Xq28	Xq28		300482	GAB3	GRB2-associated binding protein 3	GAB3	139716	ENSG00000160219			Gab3 (MGI:2387324)			
chrX	154762741	154777688	Xq28	Xq28		300126	"DKC1, DKCX"	Dyskerin	DKC1	1736	ENSG00000130826		"Dyskeratosis congenita, X-linked, 305000 (3), X-linked recessive"	Dkc1 (MGI:1861727)			
chrX	154778683	154805526	Xq28	Xq28		305360	"MPP1, PEMP, EMP55"	"Membrane protein, palmitoylated-1, 55kD"	MPP1	4354	ENSG00000130830	~30kb 3' and centromeric to F8		Mpp1 (MGI:105941)			
chrX	154835787	155022722	Xq28	Xq28		300841	"F8, F8C, HEMA"	"Coagulation factor VIII, procoagulant component"	F8	2157	ENSG00000185010	cen-G6PD-3' end of F8C-5'-ter; 1.1Mb from telomere	"Hemophilia A, 306700 (3), X-linked recessive"	F8 (MGI:88383)			
chrX	154886359	154888060	Xq28	Xq28		305423	"F8A, DXS522E, HAP40"	Factor VIII associated gene 1	F8A1	8263	ENSG00000277203	"3 copies, 1 in intron 22 of F8C"		F8a (MGI:95474)			
chrX	155064033	155071271	Xq28	Xq28		300116	MTCP1	Mature T-cell proliferation 1	MTCP1	4515	ENSG00000214827						
chrX	155071402	155126765	Xq28	Xq28		300617	"BRCC3, BRCC36"	"BRCA1/BRCA2-containing complex, subunit 3"	BRCC3	79184	ENSG00000185515			Brcc3 (MGI:2389572)			
chrX	155197006	155239840	Xq28	Xq28		300133	VBP1	Von Hippel-Lindau binding protein-1	VBP1	7411	ENSG00000155959			Vbp1 (MGI:1333804)			
chrX	155258233	155264588	Xq28	Xq28		300774	"RAB39B, MRX72, WSMN"	Ras-associated protein RAB39B	RAB39B	116442	ENSG00000155961	mutation identified in 1 WSMN family	"Mental retardation, X-linked 72, 300271 (3), X-linked recessive; ?Waisman syndrome, 311510 (3), X-linked recessive"	Rab39b (MGI:1915040)			
chrX	155276206	155334680	Xq28	Xq28		300138	"CLIC2, XAP121, MRXS32"	Chloride intracellular channel 2	CLIC2	1193	ENSG00000155962	mutation identified in 1 MRXS32 family	"?Mental retardation, X-linked, syndromic 32, 300886 (3), X-linked recessive"				
chrX	155459418	155459934	Xq28	Xq28		300445	"H2AFB, H2ABBD"	"H2A histone family, member B"	H2AFB3	83740	ENSG00000277745			"H2afb2,H2afb1,H2afb3 (MGI:3644875,MGI:3644980,MGI:3642445)"			
chrX	155489010	155612960	Xq28	Xq28		300777	"TMLHE, BBOX2, TMLH, TMLHED, AUTSX6"	Epsilon-trimethyllysine hydroxylase	TMLHE	55217	ENSG00000185973		"{Autism, susceptibility to, X-linked 6}, 300872 (3), X-linked recessive"	Tmlhe (MGI:2180203)			
chrX	155612564	155782458	Xq28	Xq28		300531	SPRY3	"Sprouty, Drosophila, homolog of, 3"	SPRY3	10251	ENSG00000168939	in pseudoautosomal region PAR2		Spry3 (MGI:1345188)			
chrX	155881279	155943768	Xq28	Xq28		300053	"VAMP7, SYBL1, TIVAMP"	Vesicle-associated membrane protein 7	VAMP7	6845	ENSG00000124333			Vamp7 (MGI:1096399)			
chrX	155997580	156013016	Xq28	Xq28		300007	IL9R	Interleukin-9 receptor	IL9R	3581	ENSG00000124334	in PAR2 pseudoautosomal region		Il9r (MGI:96564)			
chrX	0	156040895	Chr.X			300864	CCCSX	"Cerebral-cerebellar-coloboma syndrome, X-linked"		100820758			"Cerebral-cerebellar-coloboma syndrome, X-linked, 300864 (2), X-linked recessive"				
chrX	0	156040895	Chr.X			300471	CVMRF	Cubitus valgus with mental retardation and unusual facies		494028			"Cubitus valgus with mental retardation and unusual facies, 300471 (2), X-linked recessive"				
chrX	0	156040895	Chr.X			300719	DFCTRPS	"Deafness, cataract, retinitis pigmentosa, and sperm abnormalities"		100188774			"Deafness, cataract, retinitis pigmentosa, and sperm abnormalities, 300719 (2), X-linked recessive"				
chrX	0	156040895	Chr.X			300345	MCOPCB1	"Microphthalmia, isolated, with coloboma 1"		85503			"Microphthalmia with coloboma 1, 300345 (2)"				
chrX	0	156040895	Chr.X			300716	MRX95	"Mental retardation, X-linked 95"		102775568			"Mental retardation, X-linked 95, 300716 (2), X-linked dominant"				
chrX	0	156040895	Chr.X			300612	MRXSBWB	Brooks-Wisniewski-Brown syndrome		105463128			"Brooks-Wisniewski-Brown syndrome, 300612 (2), X-linked recessive"				
chrX	0	156040895	Chr.X			300519	MRXSMP	"Mental retardation, X-linked, syndromic, Martin-Probst type"		574047			"Mental retardation, X-linked, syndromic, Martin-Probst type, 300519 (2), X-linked recessive"				
chrX	0	156040895	Chr.X			300331	THCYTX	"Thrombocythemia, X-linked"		84434			"Thrombocythemia, X-linked, 300331 (2), X-linked recessive"				
chrY	0	300000	Yp11.32			400046	PLCXD1Y	"Phospholipase C, phosphatidylinositol-specific, X domain-containing protein 1"				in pseudoautosomal region					
chrY	0	10400000	Yp11			489500	XGR	XG regulator	XGR	7501		in pseudoautosomal region					
chrY	624343	659410	Ypter-p11.2	Yp11.2		400020	SHOXY	"Short stature homeo box, Y-linked"	SHOX	6473	ENSG00000185960	pseudoautosomal	"Langer mesomelic dysplasia, 249700 (3), Autosomal recessive; Leri-Weill dyschondrosteosis, 127300 (3), Autosomal dominant; Short stature, idiopathic familial, 300582 (3)"				
chrY	1190436	1212761	Yp11.3	Yp11.2		400023	CRLF2Y	"Cytokine receptor-like factor 2, Y-linked"	CRLF2	64109	ENSG00000205755	pseudoautosomal		Crlf2 (MGI:1889506)			
chrY	1268799	1325096	Yp11	Yp11.2		425000	CSF2RY	"Granulocyte-macrophage colony-stimulating factor receptor, alpha subunit (Y chromosome)"	CSF2RA	1438	ENSG00000198223	306250 = X homolog; distal to MIC2Y		Csf2ra (MGI:1339754)			
chrY	1336573	1382688	Yp11.3	Yp11.2		430000	"IL3RA, IL3RY, IL3RAY"	Interleukin-3 receptor (Y chromosome)	IL3RA	3563	ENSG00000185291	308385 = X homolog; pseudoautosomal		Il3ra (MGI:96553)			
chrY	1386151	1392145	Yp	Yp11.2		403000	ANT3Y	Adenine nucleotide translocator-3 (Y chromosome)	SLC25A6	293	ENSG00000169100	300151 = X homolog; proximal to CSF2RY					
chrY	1403138	1453793	Ypter-p11.2	Yp11.2		400011	ASMTLY	"Acetylserotonin methyltransferase-like, Y-linked"	ASMTL	8623	ENSG00000169093						
chrY	1591592	1602519	Ypter-p11.2	Yp11.2		465000	"AKAP17A, SFRS17A, XE7Y"	A kinase (PRKA) anchor protein 17A	AKAP17A	8227	ENSG00000197976	see 300015 locus					
chrY	1595454	1643080	Ypter-p11.2	Yp11.2		402500	ASMTY	Acetylserotonin methyltransferase (Y chromosome)	ASMT	438	ENSG00000196433	pseudoautosomal					
chrY	2691132	2741308	Ypter-p11.2	Yp11.2		450000	MIC2Y	"Antigen identified by monoclonal 12E7, Y homolog"	CD99	4267	ENSG00000002586	pseudoautosomal					
chrY	2786854	2787740	Yp11.3	Yp11.2		480000	"SRY, TDF, TDY, SRXX1, SRXY1"	Sex-determining region Y (testis determining factor)	SRY	6736	ENSG00000184895		"46XX sex reversal 1, 400045 (3); 46XY sex reversal 1, 400044 (3)"				
chrY	2841581	2866955	Yp11.3	Yp11.2		470000	RPS4Y1	"Ribosomal protein S4, Y-linked, 1"	RPS4Y1	6192	ENSG00000129824			Rps4x (MGI:98158)			
chrY	2934401	2982507	Yp11.3	Yp11.2		490000	ZFY	"Zinc finger protein, Y-linked"	ZFY	7544	ENSG00000067646						
chrY	3579084	3580040	Yp11.2	Yp11.2		400025	"TGIF2LY, TGIFLY"	"Transforming growth factor-beta-induced factor 2-like, Y-linked"	TGIF2LY	90655	ENSG00000176679						
chrY	5000043	5742227	Yp11.2	Yp11.2		400022	"PCDH11Y, PCDH22, PCDHY"	Protocadherin 22	PCDH11Y	83259	ENSG00000099715						
chrY	6865917	6874055	Yp11	Yp11.2		410000	"AMELY, AMGL"	Amelogenin (Y chromosome)	AMELY	266	ENSG00000099721	301200 = X homolog		Amelx (MGI:88005)			
chrY	6908593	7107153	Yp11.2	Yp11.2		400033	TBL1Y	"Transducin-beta-like 1, Y-linked"	TBL1Y	90665	ENSG00000092377						
chrY	7273971	7381546	Yp11.2	Yp11.2		400008	PRKY	"Protein kinase, Y-linked"	PRKY	5616							
chrY	9466954	9469755	Ypter-p11.2	Yp11.2		480100	"TSPY1, TSPY"	"Testis-specific protein, Y-linked, 1"	TSPY1	7258	ENSG00000258992						
chrY	10400000	26600000	Yq11			400042	"DELYq11, CYDELq11, SPGFY1"	Chromosome Yq11 interstitial deletion syndrome				contiguous gene deletion syndrome	"Spermatogenic failure, Y-linked, 1, 400042 (4)"				
chrY	10400000	57227415	Yq			425500	HEY	"Hairy ears, Y-linked"		100188776			"?Hairy ears, Y-linked, 425500 (2), Y-linked"				
chrY	10600000	26600000	Yq11.2			400032	CYorf15B	Chromosome Y open reading frame 15B									
chrY	12701230	12860842	Yq11.2	Yq11.221		400005	"USP9Y, DFFRY, SPGFY2"	"Ubiquitin-specific protease-9, Y chromosome (Drosophila fat facets related, Y-linked)"	USP9Y	8287	ENSG00000114374		"Spermatogenic failure, Y-linked, 2, 415000 (3), Y-linked"	Usp9y (MGI:1313274)			
chrY	12903998	12920477	Yq11	Yq11.221		400010	"DDX3Y, DBY"	"DEAD/H box-3, Y-linked"	DDX3Y	8653	ENSG00000067048			Ddx3y (MGI:1349406)			
chrY	13231826	13480669	Yq11	Yq11.221		400009	UTY	Ubiquitously transcribed TPR gene on Y chromosome	UTY	7404	ENSG00000183878						
chrY	13703566	13706023	Yq11.221	Yq11.221		400017	TMSB4Y	"Thymosin, beta-4, Y chromosome"	TMSB4Y	9087	ENSG00000154620						
chrY	13985771	13986511	Yq11.221	Yq11.221		400012	"VCY, BPY1"	"Variably charged, Y chromosome"	VCY	9084	ENSG00000129864						
chrY	14522577	14845646	Yq11.2	Yq11.221		400028	"NLGN4Y, KIAA0951"	"Neuroligin 4, Y-linked"	NLGN4Y	22829	ENSG00000165246						
chrY	17768979	17770559	Yq11.222	Yq11.222		400015	XKRY	XK-related protein on Y chromosome	XKRY	9082	ENSG00000250868						
chrY	18025786	18027745	Yq11.221	Yq11.222		400018	CDY2	"Chromodomain protein, Y chromosome, 2"	CDY2A	9426	ENSG00000182415						
chrY	18529677	18588962	Yq11.2	Yq11.222		400029	HSFY	"Heat shock transcription factor, Y-linked"	HSFY1	86614	ENSG00000172468			Hsfy2 (MGI:1918316)			
chrY	19567357	19607169	Yq11.2	Yq11.222-q11.223		400031	CYorf15A	Chromosome Y open reading frame 15A	TXLNGY	246126							
chrY	19705414	19745340	Yq11	Yq11.223		426000	"KDM5D, JARID1D, SMCY, HYA"	Lysine-specific demethylase 5D	KDM5D	8284	ENSG00000012817	encodes H-Y epitope in mouse		Kdm5d (MGI:99780)			
chrY	20575710	20593153	Yq11.223	Yq11.223		400014	EIF1AY	"Eukaryotic translation initiation factor 1A, Y isoform"	EIF1AY	9086	ENSG00000198692			Eif1ax (MGI:1913485)			
chrY	20756067	20781031	Yq11.2	Yq11.223		400030	RPS4Y2	"Ribosomal protein S4, Y-linked"	RPS4Y2	140032	ENSG00000280969						
chrY	21534878	21559682	Yq11	Yq11.223		400006	"RBMY1A1, RBM1, YRRM1, RBM2"	"RNA binding motif protein, Y chromosome, family 1, member A1"	RBMY1A1	5940	ENSG00000234414						
chrY	22071755	22096006	Yq11.2	Yq11.223		400041	PRY2	"PTPBL-related gene on Y, 2"	PRY2	442862	ENSG00000169807						
chrY	22296797	22298875	Yq11.223	Yq11.223		400038	TTTY5	"Testis-specific transcript, Y-linked, 5"	TTTY5	83863							
chrY	22439592	22441458	Yq11.223	Yq11.223		400039	TTTY6	"Testis-specific transcript, Y-linked, 6"	TTTY6	84672							
chrY	22490290	22516302	Yq11.223	Yq11.223		400019	PRY	"PTPN13-like, Y-linked"	PRY	9081	ENSG00000169789						
chrY	22851583	22852714	Yq11.223	Yq11.223		400040	TTY17	"Testis-specific transcript, Y-linked, 17"	TTTY17A	252949							
chrY	22936454	22973283	Yq11.223	Yq11.223		400037	TTTY4	"Testis-specific transcript, Y-linked, 4"	TTTY4	114761							
chrY	22984262	23005464	Yq	Yq11.223		400013	BPY2	"Basic protein on Y chromosome, 2"	BPY2	9083	ENSG00000183753						
chrY	23129354	23199116	Yq11	Yq11.223		400003	DAZ	Deleted in azoospermia	DAZ1	1617	ENSG00000188120	?same as AZF	?Sertoli-cell-only syndrome (1)				
chrY	23219456	23291355	Yq11.2	Yq11.223		400026	DAZ2	Deleted in azoospermia 2	DAZ2	57055	ENSG00000205944			Dazl (MGI:1342328)			
chrY	24209966	24214830	Yq11.23	Yq11.23		400035	GOLGA2LY	"Golgi autoantigen, golgin subfamily A, 2-like, Y-linked"	GOLGA2P2Y	84559							
chrY	24763068	24813491	Yq11.2	Yq11.23		400027	DAZ3	Deleted in azoospermia 3	DAZ3	57054	ENSG00000187191						
chrY	25482907	25486704	Yq11.23	Yq11.23		400034	"CSPG4P1Y, CSPG4LY"	"Chondroitin sulfate proteoglycan 4 pseudogene 1, Y-linked"	CSPG4P1Y	114758							
chrY	25622094	25625510	Yq11.23	Yq11.23		400016	"CDY1, CDY"	"Chromodomain protein, Y chromosome"	CDY1	9085	ENSG00000172288						
chrY	25728489	25733387	Yq11.23	Yq11.23		400036	TTTY3	"Testis-specific transcript, Y-linked, 3"	TTTY3	114760							
chrY	26600000	57227415	Yq12			475000	"GCY, TSY, STA"	"Growth control, Y-chromosome influenced"	GCY	2656							
chrY	0	57227415	Chr.Y			400043	DFNY1	"Deafness, Y-linked 1"	DFNY1	724074			"Deafness, Y-linked 1 (1)"				
chrY	0	57227415	Chr.Y			400004	RPY	"Retinitis pigmentosa, Y-linked"		79051			"Retinitis pigmentosa, Y-linked, 400004 (2), Y-linked"				
#																	
#																	
#																	
#																	
# Source of data in fields are as follows:																	
# -------------------------------																	
#																	
# Chromosome (NCBI)																	
# Genomic position start * (NCBI)																	
# Genomic position end (NCBI)																	
# Cyto location (OMIM)																	
# Computed cyto location (UCSC)																	
# MIM Number for Gene/Locus (OMIM)																	
# Gene symbols (OMIM)																	
# Gene name (OMIM)																	
# Approved gene symbol (HGNC)																	
# Entrez gene ID (NCBI)																	
# Ensembl gene ID (Ensembl)																	
# Comments (OMIM)																	
# Phenotype(s) (OMIM)																	
# Mouse gene symbol & ID (MGI)																	
#																	
# * for phenotypes with mapping key of (2) or genes not found in NCBI																	
"# data, genomic coordinates are derived from OMIM's cyto location mapped"																	
# to genomic using UCSC table.																	
#																	
#																	
# OMIM Phenotype field is nested:																	
# -------------------------------																	
#																	
"# Each Phenotype is followed by its MIM number, if different from"																	
"# that of the locus, preceded by a comma"																	
# Phenotype mapping key in parentheses follows the phenotype MIM																	
# number (explanation below).																	
# Allelic disorders are separated by a semi-colon following the																	
# phenotype mapping key.																	
# Inheritance for the phenotype follows the phenotype mapping key																	
"# preceded by a ,<space>"																	
#																	
#																	
# Phenotype Mapping Method - Appears in parentheses after a disorder :																	
# --------------------------------------------------------------------																	
# 1 - the disorder is placed on the map based on its association with																	
"# a gene, but the underlying defect is not known."																	
# 2 - the disorder has been placed on the map by linkage; no mutation has																	
# been found.																	
# 3 - the molecular basis for the disorder is known; a mutation has been																	
# found in the gene.																	
"# 4 - a contiguous gene deletion or duplication syndrome, multiple genes"																	
# are deleted or duplicated causing the phenotype.																	
#																	
