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Gene: EHD1 (EH domain containing 1) Homo sapiens

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Symbol:

EHD1

Name:

EH domain containing 1

RGD ID:

1319124

HGNC Page

HGNC:3242

Description:

Enables identical protein binding activity and small GTPase binding activity. Involved in several processes, including endocytic recycling; protein homooligomerization; and protein localization to cilium. Located in ciliary pocket membrane; early endosome membrane; and recycling endosome membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

EH domain-containing protein 1; EH-domain containing 1; FLJ42622; FLJ44618; H-PAST; HPAST1; PAST; PAST homolog 1; PAST1; testilin

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Ehd1 (EH-domain containing 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Ehd1 (EH-domain containing 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ehd1 (EH domain containing 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	EHD1 (EH domain containing 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	EHD1 (EH domain containing 1)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ehd1 (EH domain containing 1)	NCBI	Ortholog
Sus scrofa (pig):	EHD1 (EH domain containing 1)	HGNC	Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	EHD1 (EH domain containing 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ehd1 (EH domain containing 1)	NCBI	Ortholog
Other homologs ²
Mus musculus (house mouse):	Ehd3 (EH-domain containing 3)	HGNC	OrthoDB, OrthoMCL
Mus musculus (house mouse):	Ehd4 (EH-domain containing 4)	HGNC	OrthoMCL
Mus musculus (house mouse):	Ehd2 (EH-domain containing 2)	HGNC	OrthoMCL
Rattus norvegicus (Norway rat):	Ehd3 (EH-domain containing 3)	HGNC	OrthoDB
Sus scrofa (pig):	EHD3 (EH domain containing 3)	HGNC	OrthoDB
Canis lupus familiaris (dog):	EHD3 (EH domain containing 3)	HGNC	OrthoDB
Rattus norvegicus (Norway rat):	Tnfrsf13c (TNF receptor superfamily member 13C)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Ehd1 (EH-domain containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Ehd1 (EH-domain containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ehd1b (EH-domain containing 1b)	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|ZFIN)
Danio rerio (zebrafish):	ehd1a (EH-domain containing 1a)	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|ZFIN)
Drosophila melanogaster (fruit fly):	Past1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	rme-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	IRS4	Alliance	DIOPT (Ensembl Compara\|PANTHER)
Saccharomyces cerevisiae (baker's yeast):	SLA1	Alliance	DIOPT (Ensembl Compara\|PANTHER)
Xenopus laevis (African clawed frog):	ehd1.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	ehd1.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	ehd1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,851,642 - 64,879,693 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,851,642 - 64,888,296 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,619,114 - 64,647,165 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	64,376,784 - 64,402,767 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	64,376,783 - 64,402,767	NCBI
Celera	11	61,946,373 - 61,972,260 (-)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,947,278 - 60,973,225 (-)	NCBI		HuRef
CHM1_1	11	64,504,028 - 64,529,958 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,844,974 - 64,872,935 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Bardet-Biedl syndrome (IAGP)

Disease Progression (EXP)

glycogen storage disease V (IAGP)

high grade glioma (EXP)

intellectual disability (IAGP)

leukocyte adhesion deficiency 3 (IAGP)

Neoplasm Recurrence, Local (EXP)

obesity (ISO)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

1,3-dinitrobenzene (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

2,4-dinitrotoluene (ISO)

2-amino-14,16-dimethyloctadecan-3-ol (EXP)

2-methylcholine (EXP)

6-propyl-2-thiouracil (ISO)

acrolein (EXP)

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP)

alpha-Zearalanol (ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

atrazine (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[a]pyrene diol epoxide I (EXP)

benzo[b]fluoranthene (ISO)

Benzo[k]fluoranthene (ISO)

bis(2-ethylhexyl) phthalate (EXP)

bisphenol A (EXP,ISO)

Bisphenol B (EXP)

bleomycin A2 (ISO)

C60 fullerene (ISO)

cadmium dichloride (EXP)

caffeine (EXP)

calcitriol (EXP)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

chrysene (ISO)

cobalt dichloride (EXP)

copper(II) chloride (EXP)

crocidolite asbestos (EXP)

cyclosporin A (EXP)

dextran sulfate (ISO)

diazinon (EXP)

Dibutyl phosphate (EXP)

dorsomorphin (EXP)

epoxiconazole (ISO)

ethanol (ISO)

folic acid (ISO)

formaldehyde (EXP)

FR900359 (EXP)

gentamycin (ISO)

ivermectin (EXP)

leflunomide (EXP)

Licochalcone B (EXP)

lipopolysaccharide (EXP,ISO)

mercury dichloride (ISO)

Mesaconitine (ISO)

methimazole (ISO)

morphine (ISO)

N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (EXP)

N-methyl-4-phenylpyridinium (ISO)

naphthalene (ISO)

nickel atom (EXP)

ozone (EXP)

paracetamol (ISO)

peptidoglycan (EXP)

perfluorohexanesulfonic acid (ISO)

perfluorooctane-1-sulfonic acid (ISO)

perfluorooctanoic acid (ISO)

phenobarbital (EXP)

phenylmercury acetate (EXP)

pirinixic acid (ISO)

potassium dichromate (EXP)

progesterone (EXP)

propiconazole (ISO)

Propiverine (ISO)

protein kinase inhibitor (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

SB 431542 (EXP)

selenomethionine (EXP)

serpentine asbestos (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

succimer (ISO)

sulfadimethoxine (ISO)

temozolomide (EXP)

tetrachloromethane (ISO)

tetraphene (ISO)

thiram (EXP)

titanium dioxide (ISO)

trichloroethene (ISO)

triphenyl phosphate (EXP)

urethane (EXP)

valproic acid (EXP,ISO)

zinc atom (EXP)

zinc sulfate (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cell projection organization (IEA)

cellular response to nerve growth factor stimulus (IEA,ISS)

cholesterol homeostasis (IEA,ISS)

cilium assembly (IBA,IDA,IEA,IMP)

endocytic recycling (IBA,IGI,IMP)

endocytosis (IBA,IEA,IMP,ISO)

endosomal transport (IEA,ISO)

intracellular protein transport (IMP)

low-density lipoprotein particle clearance (IEA,ISS)

neuron projection development (IEA,ISS)

positive regulation of cholesterol storage (IEA,ISS)

positive regulation of endocytic recycling (IEA,ISS)

positive regulation of myoblast fusion (IEA,ISS)

positive regulation of neuron projection development (IEA,ISO)

protein homooligomerization (IPI)

protein localization to cilium (IMP)

protein localization to plasma membrane (IBA)

protein transport (IEA)

Cellular Component

ciliary membrane (IEA)

ciliary pocket membrane (IDA)

cilium (IDA,IEA)

cytoplasm (IBA,IEA)

early endosome (IBA,IEA)

early endosome membrane (IDA,IEA)

endocytic vesicle (IBA,IEA)

endomembrane system (IEA)

endosome (IEA)

endosome membrane (IEA,ISS,TAS)

extracellular exosome (HDA)

glutamatergic synapse (IEA,ISO)

lipid droplet (IEA,ISS)

membrane (HDA,IEA)

perinuclear region of cytoplasm (IBA,IEA)

plasma membrane (IBA,IEA,ISS)

platelet dense tubular network membrane (IEA,ISS)

presynaptic active zone (IEA,ISO)

recycling endosome membrane (IBA,IDA,IEA)

Molecular Function

ATP binding (IEA)

cadherin binding (HDA)

calcium ion binding (IEA)

GTP binding (IEA)

identical protein binding (IPI)

metal ion binding (IEA)

protein binding (IPI,ISO)

small GTPase binding (IPI)

Molecular Pathway Annotations Click to see Annotation Detail View

endocytosis pathway (IEA)

retromer-mediated pathway (TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Ependymoma (IAGP)

Intellectual disability (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	Retromer and sorting nexins in endosomal sorting.	Gallon M and Cullen PJ, Biochem Soc Trans. 2015 Feb;43(1):33-47. doi: 10.1042/BST20140290.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	Differential expression of adipose tissue proteins between obesity-susceptible and -resistant rats fed a high-fat diet.	Joo JI, etal., Proteomics. 2011 Apr;11(8):1429-48. doi: 10.1002/pmic.201000515. Epub 2011 Feb 25.
4.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
5.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8619474	PMID:8889548	PMID:9110174	PMID:9253601	PMID:9397678	PMID:10395801	PMID:10564830	PMID:10673336	PMID:11423532	PMID:12032069	PMID:12121420	PMID:12477932
PMID:12665801	PMID:14702039	PMID:15020713	PMID:15247266	PMID:15371016	PMID:15489334	PMID:15710626	PMID:16251358	PMID:16344560	PMID:17081983	PMID:17233914	PMID:17284518
PMID:17507647	PMID:17899392	PMID:18661112	PMID:19056867	PMID:19199708	PMID:19369419	PMID:19798736	PMID:19864458	PMID:19946888	PMID:20106972	PMID:20329706	PMID:20458337
PMID:20467437	PMID:20489164	PMID:20801876	PMID:20961375	PMID:21115825	PMID:21873635	PMID:22284051	PMID:22456504	PMID:22863883	PMID:22939629	PMID:23376485	PMID:23533145
PMID:23596323	PMID:24019528	PMID:24481818	PMID:24797263	PMID:24946721	PMID:25277244	PMID:25287187	PMID:25468996	PMID:25595798	PMID:25686250	PMID:25921289	PMID:26186194
PMID:26226295	PMID:26344197	PMID:26378252	PMID:26465136	PMID:26496610	PMID:26618866	PMID:26949251	PMID:27189942	PMID:27411790	PMID:27531895	PMID:28215104	PMID:28514442
PMID:28596240	PMID:29128334	PMID:29335527	PMID:29467282	PMID:29549343	PMID:29568061	PMID:30194290	PMID:30442766	PMID:30639242	PMID:30659120	PMID:30683896	PMID:30737378
PMID:30833792	PMID:30975166	PMID:31023336	PMID:31091453	PMID:31615969	PMID:31672844	PMID:31707150	PMID:31871319	PMID:31932471	PMID:31932478	PMID:32138615	PMID:32296183
PMID:32513696	PMID:32800345	PMID:32966336	PMID:32994395	PMID:33022573	PMID:33961781	PMID:34079125	PMID:34217785	PMID:34369648	PMID:34373451	PMID:34591612	PMID:34597346
PMID:35149593	PMID:35256949	PMID:35439318	PMID:35509820	PMID:35616188	PMID:35831314	PMID:35844135	PMID:35944360	PMID:36215168	PMID:36237976	PMID:36244648	PMID:36543142
PMID:37074924	PMID:37232246	PMID:37474760	PMID:37689310	PMID:37774976	PMID:38011671	PMID:38117590	PMID:38334954	PMID:38569033	PMID:39231216

Genomics

Comparative Map Data

EHD1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,851,642 - 64,879,693 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,851,642 - 64,888,296 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,619,114 - 64,647,165 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	64,376,784 - 64,402,767 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	64,376,783 - 64,402,767	NCBI
Celera	11	61,946,373 - 61,972,260 (-)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,947,278 - 60,973,225 (-)	NCBI		HuRef
CHM1_1	11	64,504,028 - 64,529,958 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,844,974 - 64,872,935 (-)	NCBI		T2T-CHM13v2.0

Ehd1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	19	6,326,926 - 6,350,126 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	19	6,326,755 - 6,350,126 (+)	Ensembl		GRCm39 Ensembl
GRCm38	19	6,276,896 - 6,300,096 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	19	6,276,725 - 6,300,096 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	19	6,276,896 - 6,300,096 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	19	6,276,896 - 6,300,096 (+)	NCBI		MGSCv36	mm8
Celera	19	6,149,194 - 6,172,784 (+)	NCBI		Celera
Cytogenetic Map	19	A	NCBI
cM Map	19	4.4	NCBI

Ehd1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	213,009,113 - 213,031,488 (+)	NCBI		GRCr8
mRatBN7.2	1	203,579,850 - 203,602,226 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	203,579,869 - 203,602,212 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	211,928,608 - 211,950,969 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	219,025,181 - 219,047,556 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	211,716,238 - 211,738,613 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	221,644,867 - 221,667,242 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	221,644,867 - 221,667,239 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	228,632,629 - 228,655,004 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	209,055,234 - 209,077,609 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	209,213,709 - 209,234,786 (+)	NCBI
Celera	1	201,113,342 - 201,135,717 (+)	NCBI		Celera
Cytogenetic Map	1	q43	NCBI

Ehd1
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955422	20,302,655 - 20,324,591 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	20,302,409 - 20,324,591 (+)	NCBI	ChiLan1.0	ChiLan1.0

EHD1
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	66,079,274 - 66,107,007 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	67,122,242 - 67,149,976 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	60,208,840 - 60,236,513 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	63,550,258 - 63,577,252 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	63,547,286 - 63,577,252 (-)	Ensembl	panpan1.1		panPan2

EHD1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	18	52,291,304 - 52,312,787 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	52,291,327 - 52,311,526 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	50,898,642 - 50,920,115 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	53,332,471 - 53,353,954 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	53,332,477 - 53,353,942 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	52,427,459 - 52,448,913 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	52,012,970 - 52,034,432 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	52,797,390 - 52,818,875 (+)	NCBI		UU_Cfam_GSD_1.0

Ehd1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	8,007,727 - 8,029,462 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936599	4,450,188 - 4,473,738 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936599	4,451,207 - 4,473,078 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

EHD1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	7,298,208 - 7,321,576 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	7,299,295 - 7,321,580 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	6,430,635 - 6,454,134 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

EHD1
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	9,356,128 - 9,382,204 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	9,356,177 - 9,382,832 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	106,742,061 - 106,769,019 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ehd1
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624767	21,522,750 - 21,544,133 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624767	21,522,871 - 21,543,925 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in EHD1
44 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_006795.3(EHD1):c.1546G>A (p.Glu516Lys)	single nucleotide variant	Malignant melanoma [RCV000069599]	Chr11:64854392 [GRCh38] Chr11:64621864 [GRCh37] Chr11:64378440 [NCBI36] Chr11:11q13.1	not provided
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
GRCh37/hg19 11q13.1(chr11:64485197-64691737)x3	copy number gain	See cases [RCV000203413]	Chr11:64485197..64691737 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_006795.4(EHD1):c.430C>G (p.Pro144Ala)	single nucleotide variant	not specified [RCV004298641]	Chr11:64874493 [GRCh38] Chr11:64641965 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.176C>T (p.Pro59Leu)	single nucleotide variant	not specified [RCV004309585]	Chr11:64878289 [GRCh38] Chr11:64645761 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11q13.1(chr11:64544135-64622868)x3	copy number gain	not provided [RCV000750078]	Chr11:64544135..64622868 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.246C>G (p.Asp82Glu)	single nucleotide variant	not specified [RCV004296217]	Chr11:64878219 [GRCh38] Chr11:64645691 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1005= (p.Leu335=)	variation	not provided [RCV000948865]	Chr11:64855397 [GRCh38] Chr11:64622869 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.66= (p.Ala22=)	variation	not provided [RCV000948866]	Chr11:64878399 [GRCh38] Chr11:64645871 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.1119G>A (p.Ala373=)	single nucleotide variant	not provided [RCV000927298]	Chr11:64854819 [GRCh38] Chr11:64622291 [GRCh37] Chr11:11q13.1	likely benign
NM_006795.4(EHD1):c.1392C>T (p.Gly464=)	single nucleotide variant	not provided [RCV000965190]	Chr11:64854546 [GRCh38] Chr11:64622018 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.1437C>T (p.Thr479=)	single nucleotide variant	not provided [RCV000939097]	Chr11:64854501 [GRCh38] Chr11:64621973 [GRCh37] Chr11:11q13.1	likely benign
NM_006795.4(EHD1):c.342C>G (p.Leu114=)	single nucleotide variant	not provided [RCV000965840]	Chr11:64878123 [GRCh38] Chr11:64645595 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.559C>T (p.Leu187=)	single nucleotide variant	not provided [RCV000879048]	Chr11:64860280 [GRCh38] Chr11:64627752 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.1080+9G>A	single nucleotide variant	not provided [RCV000959982]	Chr11:64855313 [GRCh38] Chr11:64622785 [GRCh37] Chr11:11q13.1	benign
dup(11)(q13.1q13.1)	duplication	Ependymoma [RCV000785872]	Chr11:63533279..65429676 [GRCh37] Chr11:11q13.1	likely pathogenic
GRCh37/hg19 11q13.1-13.2(chr11:64501919-67129258)x3	copy number gain	See cases [RCV000511632]	Chr11:64501919..67129258 [GRCh37] Chr11:11q13.1-13.2	likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_006795.4(EHD1):c.819C>G (p.Ala273=)	single nucleotide variant	not provided [RCV000965191]	Chr11:64860020 [GRCh38] Chr11:64627492 [GRCh37] Chr11:11q13.1	benign
NM_006795.4(EHD1):c.1302C>T (p.Ile434=)	single nucleotide variant	not provided [RCV000924143]	Chr11:64854636 [GRCh38] Chr11:64622108 [GRCh37] Chr11:11q13.1	likely benign
NC_000011.9:g.(?_59596957)_(68707199_?)dup	duplication	Familial temporal lobe epilepsy 8 [RCV001372442]	Chr11:59596957..68707199 [GRCh37] Chr11:11q12.1-13.3	uncertain significance
NC_000011.9:g.(?_64522783)_(66283694_?)del	deletion	Bardet-Biedl syndrome [RCV002014493]\|Glycogen storage disease, type V [RCV002004587]	Chr11:64522783..66283694 [GRCh37] Chr11:11q13.1-13.2	pathogenic
NC_000011.9:g.(?_58916346)_(64972349_?)dup	duplication	Leukocyte adhesion deficiency 3 [RCV003113394]\|not provided [RCV003113393]	Chr11:58916346..64972349 [GRCh37] Chr11:11q12.1-13.1	uncertain significance\|no classifications from unflagged records
NM_006795.4(EHD1):c.115C>T (p.His39Tyr)	single nucleotide variant	not specified [RCV004306460]	Chr11:64878350 [GRCh38] Chr11:64645822 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1308C>T (p.Asp436=)	single nucleotide variant	not provided [RCV000961066]	Chr11:64854630 [GRCh38] Chr11:64622102 [GRCh37] Chr11:11q13.1	likely benign
GRCh37/hg19 11q13.1(chr11:64396501-64883447)x3	copy number gain	not provided [RCV000848683]	Chr11:64396501..64883447 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.232C>T (p.Leu78=)	single nucleotide variant	not provided [RCV000911405]	Chr11:64878233 [GRCh38] Chr11:64645705 [GRCh37] Chr11:11q13.1	likely benign
NM_006795.4(EHD1):c.1193G>A (p.Arg398Gln)	single nucleotide variant	not specified [RCV004200395]	Chr11:64854745 [GRCh38] Chr11:64622217 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.673G>A (p.Glu225Lys)	single nucleotide variant	not specified [RCV004217161]	Chr11:64860166 [GRCh38] Chr11:64627638 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1337C>T (p.Pro446Leu)	single nucleotide variant	not specified [RCV004223837]	Chr11:64854601 [GRCh38] Chr11:64622073 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1393G>A (p.Ala465Thr)	single nucleotide variant	not specified [RCV004145008]	Chr11:64854545 [GRCh38] Chr11:64622017 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1291G>A (p.Gly431Ser)	single nucleotide variant	not specified [RCV004126392]	Chr11:64854647 [GRCh38] Chr11:64622119 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.844A>G (p.Ile282Val)	single nucleotide variant	not specified [RCV004143866]	Chr11:64859995 [GRCh38] Chr11:64627467 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.227G>A (p.Arg76Gln)	single nucleotide variant	not specified [RCV004127658]	Chr11:64878238 [GRCh38] Chr11:64645710 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1576G>T (p.Val526Leu)	single nucleotide variant	not specified [RCV004095428]	Chr11:64854362 [GRCh38] Chr11:64621834 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.977G>A (p.Ser326Asn)	single nucleotide variant	not specified [RCV004217870]	Chr11:64855425 [GRCh38] Chr11:64622897 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1468G>A (p.Val490Met)	single nucleotide variant	not specified [RCV004279531]	Chr11:64854470 [GRCh38] Chr11:64621942 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.899G>A (p.Arg300Gln)	single nucleotide variant	not specified [RCV004357095]	Chr11:64859940 [GRCh38] Chr11:64627412 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q13.1(chr11:64573225-65193732)x3	copy number gain	not provided [RCV003484844]	Chr11:64573225..65193732 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1031G>A (p.Arg344His)	single nucleotide variant	not specified [RCV004377591]	Chr11:64855371 [GRCh38] Chr11:64622843 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1069C>T (p.Arg357Cys)	single nucleotide variant	not specified [RCV004377592]	Chr11:64855333 [GRCh38] Chr11:64622805 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1165G>A (p.Asp389Asn)	single nucleotide variant	not specified [RCV004377594]	Chr11:64854773 [GRCh38] Chr11:64622245 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1168A>G (p.Ile390Val)	single nucleotide variant	not specified [RCV004377596]	Chr11:64854770 [GRCh38] Chr11:64622242 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1198G>A (p.Glu400Lys)	single nucleotide variant	not specified [RCV004377597]	Chr11:64854740 [GRCh38] Chr11:64622212 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1204T>A (p.Ser402Thr)	single nucleotide variant	not specified [RCV004377598]	Chr11:64854734 [GRCh38] Chr11:64622206 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1484T>G (p.Leu495Arg)	single nucleotide variant	not specified [RCV004622491]	Chr11:64854454 [GRCh38] Chr11:64621926 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1367C>A (p.Ser456Tyr)	single nucleotide variant	not specified [RCV004622492]	Chr11:64854571 [GRCh38] Chr11:64622043 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.911C>G (p.Ala304Gly)	single nucleotide variant	not specified [RCV004622493]	Chr11:64859928 [GRCh38] Chr11:64627400 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1118C>T (p.Ala373Val)	single nucleotide variant	not specified [RCV004377593]	Chr11:64854820 [GRCh38] Chr11:64622292 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
NM_006795.4(EHD1):c.266G>A (p.Gly89Glu)	single nucleotide variant	not specified [RCV004183378]	Chr11:64878199 [GRCh38] Chr11:64645671 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.122G>A (p.Arg41His)	single nucleotide variant	not specified [RCV004071408]	Chr11:64878343 [GRCh38] Chr11:64645815 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.212A>G (p.Lys71Arg)	single nucleotide variant	not specified [RCV004073645]	Chr11:64878253 [GRCh38] Chr11:64645725 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.676A>G (p.Thr226Ala)	single nucleotide variant	not specified [RCV004225020]	Chr11:64860163 [GRCh38] Chr11:64627635 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1208T>C (p.Leu403Pro)	single nucleotide variant	not specified [RCV004344475]	Chr11:64854730 [GRCh38] Chr11:64622202 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.424C>T (p.Pro142Ser)	single nucleotide variant	not specified [RCV004362384]	Chr11:64874499 [GRCh38] Chr11:64641971 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1007G>T (p.Gly336Val)	single nucleotide variant	not specified [RCV004344125]	Chr11:64855395 [GRCh38] Chr11:64622867 [GRCh37] Chr11:11q13.1	uncertain significance
NM_006795.4(EHD1):c.1262C>T (p.Pro421Leu)	single nucleotide variant	not specified [RCV004352700]	Chr11:64854676 [GRCh38] Chr11:64622148 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q13.1(chr11:64557855-64741375)x3	copy number gain	not provided [RCV003484843]	Chr11:64557855..64741375 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3	copy number gain	not provided [RCV003484842]	Chr11:59923608..76272324 [GRCh37] Chr11:11q12.2-13.5	pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3	copy number gain	not specified [RCV003986944]	Chr11:56895955..69295402 [GRCh37] Chr11:11q12.1-13.3	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	5701
Count of miRNA genes:	1186
Interacting mature miRNAs:	1550
Transcripts:	ENST00000320631, ENST00000359393, ENST00000411683, ENST00000421510, ENST00000433803, ENST00000455148, ENST00000457202, ENST00000466015, ENST00000484846, ENST00000488711, ENST00000489379, ENST00000498472
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1357380	BW64_H	Body weight QTL 64 (human)	2.2		Body weight	percent fat after exercise training	11	60978937	86978937	Human

Markers in Region

SHGC-132442

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,331 - 64,620,617	UniSTS	GRCh37
Build 36	11	64,376,907 - 64,377,193	RGD	NCBI36
Celera	11	61,946,496 - 61,946,782	RGD
Cytogenetic Map	11	q13	UniSTS
TNG Radiation Hybrid Map	11	28606.0	UniSTS

A005R01

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,234 - 64,620,346	UniSTS	GRCh37
Build 36	11	64,376,810 - 64,376,922	RGD	NCBI36
Celera	11	61,946,399 - 61,946,511	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,304 - 60,947,416	UniSTS
GeneMap99-GB4 RH Map	11	238.17	UniSTS
NCBI RH Map	11	573.2	UniSTS

SHGC-31898

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,231 - 64,620,357	UniSTS	GRCh37
Build 36	11	64,376,807 - 64,376,933	RGD	NCBI36
Celera	11	61,946,396 - 61,946,522	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,301 - 60,947,427	UniSTS
Whitehead-RH Map	11	327.4	UniSTS
GeneMap99-G3 RH Map	11	2805.0	UniSTS

ECD00391

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,104 - 64,644,013	UniSTS	GRCh37
Build 36	11	64,399,680 - 64,400,589	RGD	NCBI36
Celera	11	61,969,173 - 61,970,082	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,970,138 - 60,971,047	UniSTS

ECD00673

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,641,808 - 64,642,702	UniSTS	GRCh37
Build 36	11	64,398,384 - 64,399,278	RGD	NCBI36
Celera	11	61,967,877 - 61,968,771	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,968,842 - 60,969,736	UniSTS

ECD01723

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,082 - 64,645,937	UniSTS	GRCh37
Build 36	11	64,401,658 - 64,402,513	RGD	NCBI36
Celera	11	61,971,151 - 61,972,006	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,116 - 60,972,971	UniSTS

ECD01882

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,755 - 64,624,604	UniSTS	GRCh37
Build 36	11	64,380,331 - 64,381,180	RGD	NCBI36
Celera	11	61,949,824 - 61,950,673	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,729 - 60,951,578	UniSTS

ECD01990

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,277 - 64,633,122	UniSTS	GRCh37
Build 36	11	64,388,853 - 64,389,698	RGD	NCBI36
Celera	11	61,958,345 - 61,959,190	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,256 - 60,960,101	UniSTS

ECD02720

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,627,018 - 64,627,837	UniSTS	GRCh37
Build 36	11	64,383,594 - 64,384,413	RGD	NCBI36
Celera	11	61,953,086 - 61,953,905	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,953,996 - 60,954,815	UniSTS

ECD03087

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,235 - 64,645,041	UniSTS	GRCh37
Build 36	11	64,400,811 - 64,401,617	RGD	NCBI36
Celera	11	61,970,304 - 61,971,110	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,269 - 60,972,075	UniSTS

ECD03554

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,630,371 - 64,631,162	UniSTS	GRCh37
Build 36	11	64,386,947 - 64,387,738	RGD	NCBI36
Celera	11	61,956,439 - 61,957,230	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,957,350 - 60,958,141	UniSTS

ECD04427

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,472 - 64,632,236	UniSTS	GRCh37
Build 36	11	64,388,048 - 64,388,812	RGD	NCBI36
Celera	11	61,957,540 - 61,958,304	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,451 - 60,959,215	UniSTS

ECD05088

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,031 - 64,638,776	UniSTS	GRCh37
Build 36	11	64,394,607 - 64,395,352	RGD	NCBI36
Celera	11	61,964,099 - 61,964,844	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,108 - 60,965,853	UniSTS

ECD05269

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,693 - 64,622,433	UniSTS	GRCh37
Build 36	11	64,378,269 - 64,379,009	RGD	NCBI36
Celera	11	61,947,858 - 61,948,598	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,763 - 60,949,503	UniSTS

ECD05595

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,871 - 64,647,602	UniSTS	GRCh37
Build 36	11	64,403,447 - 64,404,178	RGD	NCBI36
Celera	11	61,972,940 - 61,973,673	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,905 - 60,974,638	UniSTS

ECD05868

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,172 - 64,620,896	UniSTS	GRCh37
Build 36	11	64,376,748 - 64,377,472	RGD	NCBI36
Celera	11	61,946,337 - 61,947,061	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,242 - 60,947,966	UniSTS

ECD05990

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,120 - 64,646,840	UniSTS	GRCh37
Build 36	11	64,402,696 - 64,403,416	RGD	NCBI36
Celera	11	61,972,189 - 61,972,909	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,154 - 60,973,874	UniSTS

ECD06594

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,922 - 64,621,626	UniSTS	GRCh37
Build 36	11	64,377,498 - 64,378,202	RGD	NCBI36
Celera	11	61,947,087 - 61,947,791	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,992 - 60,948,696	UniSTS

ECD07777

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,635,196 - 64,635,868	UniSTS	GRCh37
Build 36	11	64,391,772 - 64,392,444	RGD	NCBI36
Celera	11	61,961,264 - 61,961,936	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,175 - 60,962,847	UniSTS

ECD08191

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,864 - 64,639,525	UniSTS	GRCh37
Build 36	11	64,395,440 - 64,396,101	RGD	NCBI36
Celera	11	61,964,932 - 61,965,593	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,941 - 60,966,602	UniSTS

ECD10749

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,637,192 - 64,637,784	UniSTS	GRCh37
Build 36	11	64,393,768 - 64,394,360	RGD	NCBI36
Celera	11	61,963,260 - 61,963,852	RGD
Cytogenetic Map	11	q13	UniSTS

ECD10815

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,626,009 - 64,626,599	UniSTS	GRCh37
Build 36	11	64,382,585 - 64,383,175	RGD	NCBI36
Celera	11	61,952,077 - 61,952,667	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,952,987 - 60,953,577	UniSTS

ECD11090

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,639,968 - 64,640,550	UniSTS	GRCh37
Build 36	11	64,396,544 - 64,397,126	RGD	NCBI36
Celera	11	61,966,036 - 61,966,618	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,045 - 60,967,627	UniSTS

ECD11872

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,624,934 - 64,625,493	UniSTS	GRCh37
Build 36	11	64,381,510 - 64,382,069	RGD	NCBI36
Celera	11	61,951,003 - 61,951,562	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,951,908 - 60,952,467	UniSTS

ECD12120

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,578 - 64,641,130	UniSTS	GRCh37
Build 36	11	64,397,154 - 64,397,706	RGD	NCBI36
Celera	11	61,966,646 - 61,967,198	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,655 - 60,968,207	UniSTS

ECD15419

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,482 - 64,636,952	UniSTS	GRCh37
Build 36	11	64,393,058 - 64,393,528	RGD	NCBI36
Celera	11	61,962,550 - 61,963,020	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,963,461 - 60,963,931	UniSTS

ECD16345

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,629,707 - 64,630,151	UniSTS	GRCh37
GRCh37	11	64,629,707 - 64,630,111	UniSTS	GRCh37
Build 36	11	64,386,283 - 64,386,687	RGD	NCBI36
Celera	11	61,955,775 - 61,956,219	UniSTS
Celera	11	61,955,775 - 61,956,179	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,956,686 - 60,957,090	UniSTS
HuRef	11	60,956,686 - 60,957,130	UniSTS

ECD19079

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,628,690 - 64,629,025	UniSTS	GRCh37
Build 36	11	64,385,266 - 64,385,601	RGD	NCBI36
Celera	11	61,954,758 - 61,955,093	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,955,669 - 60,956,004	UniSTS

REN56718

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,619,729 - 64,619,977	UniSTS	GRCh37
Build 36	11	64,376,305 - 64,376,553	RGD	NCBI36
Celera	11	61,945,893 - 61,946,142	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,946,798 - 60,947,047	UniSTS

REN56719

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,619,960 - 64,620,201	UniSTS	GRCh37
Build 36	11	64,376,536 - 64,376,777	RGD	NCBI36
Celera	11	61,946,125 - 61,946,366	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,030 - 60,947,271	UniSTS

REN56720

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,200 - 64,620,455	UniSTS	GRCh37
Build 36	11	64,376,776 - 64,377,031	RGD	NCBI36
Celera	11	61,946,365 - 61,946,620	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,270 - 60,947,525	UniSTS

REN56721

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,443 - 64,620,696	UniSTS	GRCh37
Build 36	11	64,377,019 - 64,377,272	RGD	NCBI36
Celera	11	61,946,608 - 61,946,861	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,513 - 60,947,766	UniSTS

REN56722

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,687 - 64,620,938	UniSTS	GRCh37
Build 36	11	64,377,263 - 64,377,514	RGD	NCBI36
Celera	11	61,946,852 - 61,947,103	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,757 - 60,948,008	UniSTS

REN56723

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,912 - 64,621,157	UniSTS	GRCh37
Build 36	11	64,377,488 - 64,377,733	RGD	NCBI36
Celera	11	61,947,077 - 61,947,322	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,982 - 60,948,227	UniSTS

REN56724

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,133 - 64,621,381	UniSTS	GRCh37
Build 36	11	64,377,709 - 64,377,957	RGD	NCBI36
Celera	11	61,947,298 - 61,947,546	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,203 - 60,948,451	UniSTS

REN56725

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,359 - 64,621,606	UniSTS	GRCh37
Build 36	11	64,377,935 - 64,378,182	RGD	NCBI36
Celera	11	61,947,524 - 61,947,771	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,429 - 60,948,676	UniSTS

REN56726

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,594 - 64,621,826	UniSTS	GRCh37
Build 36	11	64,378,170 - 64,378,402	RGD	NCBI36
Celera	11	61,947,759 - 61,947,991	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,664 - 60,948,896	UniSTS

REN56727

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,807 - 64,622,073	UniSTS	GRCh37
Build 36	11	64,378,383 - 64,378,649	RGD	NCBI36
Celera	11	61,947,972 - 61,948,238	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,877 - 60,949,143	UniSTS

REN56728

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,622,063 - 64,622,319	UniSTS	GRCh37
Build 36	11	64,378,639 - 64,378,895	RGD	NCBI36
Celera	11	61,948,228 - 61,948,484	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,949,133 - 60,949,389	UniSTS

REN56729

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,622,299 - 64,622,552	UniSTS	GRCh37
Build 36	11	64,378,875 - 64,379,128	RGD	NCBI36
Celera	11	61,948,464 - 61,948,717	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,949,369 - 60,949,622	UniSTS

REN56730

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,622,539 - 64,622,803	UniSTS	GRCh37
Build 36	11	64,379,115 - 64,379,379	RGD	NCBI36
Celera	11	61,948,704 - 61,948,968	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,949,609 - 60,949,873	UniSTS

REN56731

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,622,783 - 64,623,043	UniSTS	GRCh37
Build 36	11	64,379,359 - 64,379,619	RGD	NCBI36
Celera	11	61,948,948 - 61,949,208	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,949,853 - 60,950,113	UniSTS

REN56732

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,027 - 64,623,279	UniSTS	GRCh37
Build 36	11	64,379,603 - 64,379,855	RGD	NCBI36
Celera	11	61,949,192 - 61,949,444	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,097 - 60,950,349	UniSTS

REN56734

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,503 - 64,623,579	UniSTS	GRCh37
GRCh37	11	64,623,318 - 64,623,579	UniSTS	GRCh37
Build 36	11	64,379,894 - 64,380,155	RGD	NCBI36
Celera	11	61,949,572 - 61,949,648	UniSTS
Celera	11	61,949,483 - 61,949,648	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,388 - 60,950,553	UniSTS
HuRef	11	60,950,477 - 60,950,553	UniSTS

REN56735

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,561 - 64,623,796	UniSTS	GRCh37
Build 36	11	64,380,137 - 64,380,372	RGD	NCBI36
Celera	11	61,949,630 - 61,949,865	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,535 - 60,950,770	UniSTS

REN56736

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,777 - 64,624,007	UniSTS	GRCh37
Build 36	11	64,380,353 - 64,380,583	RGD	NCBI36
Celera	11	61,949,846 - 61,950,076	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,751 - 60,950,981	UniSTS

REN56737

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,623,986 - 64,624,254	UniSTS	GRCh37
Build 36	11	64,380,562 - 64,380,830	RGD	NCBI36
Celera	11	61,950,055 - 61,950,323	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,950,960 - 60,951,228	UniSTS

REN56738

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,624,235 - 64,624,474	UniSTS	GRCh37
Build 36	11	64,380,811 - 64,381,050	RGD	NCBI36
Celera	11	61,950,304 - 61,950,543	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,951,209 - 60,951,448	UniSTS

REN56739

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,624,348 - 64,624,604	UniSTS	GRCh37
Build 36	11	64,380,924 - 64,381,180	RGD	NCBI36
Celera	11	61,950,417 - 61,950,673	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,951,322 - 60,951,578	UniSTS

REN56740

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,624,937 - 64,625,164	UniSTS	GRCh37
Build 36	11	64,381,513 - 64,381,740	RGD	NCBI36
Celera	11	61,951,006 - 61,951,233	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,951,911 - 60,952,138	UniSTS

REN56741

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,625,151 - 64,625,410	UniSTS	GRCh37
Build 36	11	64,381,727 - 64,381,986	RGD	NCBI36
Celera	11	61,951,220 - 61,951,479	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,952,125 - 60,952,384	UniSTS

REN56742

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,625,320 - 64,625,548	UniSTS	GRCh37
Build 36	11	64,381,896 - 64,382,124	RGD	NCBI36
Celera	11	61,951,389 - 61,951,616	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,952,294 - 60,952,521	UniSTS

REN56743

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,625,957 - 64,626,203	UniSTS	GRCh37
Build 36	11	64,382,533 - 64,382,779	RGD	NCBI36
Celera	11	61,952,025 - 61,952,271	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,952,935 - 60,953,181	UniSTS

REN56744

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,626,193 - 64,626,429	UniSTS	GRCh37
Build 36	11	64,382,769 - 64,383,005	RGD	NCBI36
Celera	11	61,952,261 - 61,952,497	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,953,171 - 60,953,407	UniSTS

REN56745

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,626,405 - 64,626,653	UniSTS	GRCh37
Build 36	11	64,382,981 - 64,383,229	RGD	NCBI36
Celera	11	61,952,473 - 61,952,721	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,953,383 - 60,953,631	UniSTS

REN56746

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,626,517 - 64,626,749	UniSTS	GRCh37
Build 36	11	64,383,093 - 64,383,325	RGD	NCBI36
Celera	11	61,952,585 - 61,952,817	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,953,495 - 60,953,727	UniSTS

REN56747

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,626,976 - 64,627,225	UniSTS	GRCh37
Build 36	11	64,383,552 - 64,383,801	RGD	NCBI36
Celera	11	61,953,044 - 61,953,293	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,953,954 - 60,954,203	UniSTS

REN56748

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,627,189 - 64,627,440	UniSTS	GRCh37
Build 36	11	64,383,765 - 64,384,016	RGD	NCBI36
Celera	11	61,953,257 - 61,953,508	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,954,167 - 60,954,418	UniSTS

REN56749

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,627,418 - 64,627,655	UniSTS	GRCh37
Build 36	11	64,383,994 - 64,384,231	RGD	NCBI36
Celera	11	61,953,486 - 61,953,723	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,954,396 - 60,954,633	UniSTS

REN56750

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,627,634 - 64,627,878	UniSTS	GRCh37
Build 36	11	64,384,210 - 64,384,454	RGD	NCBI36
Celera	11	61,953,702 - 61,953,946	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,954,612 - 60,954,856	UniSTS

REN56751

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,627,683 - 64,627,932	UniSTS	GRCh37
Build 36	11	64,384,259 - 64,384,508	RGD	NCBI36
Celera	11	61,953,751 - 61,954,000	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,954,661 - 60,954,910	UniSTS

REN56752

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,628,681 - 64,628,908	UniSTS	GRCh37
Build 36	11	64,385,257 - 64,385,484	RGD	NCBI36
Celera	11	61,954,749 - 61,954,976	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,955,660 - 60,955,887	UniSTS

REN56753

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,628,876 - 64,629,144	UniSTS	GRCh37
Build 36	11	64,385,452 - 64,385,720	RGD	NCBI36
Celera	11	61,954,944 - 61,955,212	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,955,855 - 60,956,123	UniSTS

REN56754

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,629,110 - 64,629,357	UniSTS	GRCh37
Build 36	11	64,385,686 - 64,385,933	RGD	NCBI36
Celera	11	61,955,178 - 61,955,425	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,956,089 - 60,956,336	UniSTS

REN56755

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,629,575 - 64,629,801	UniSTS	GRCh37
Build 36	11	64,386,151 - 64,386,377	RGD	NCBI36
Celera	11	61,955,643 - 61,955,869	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,956,554 - 60,956,780	UniSTS

REN56756

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,629,785 - 64,630,022	UniSTS	GRCh37
Build 36	11	64,386,361 - 64,386,598	RGD	NCBI36
Celera	11	61,955,853 - 61,956,090	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,956,764 - 60,957,001	UniSTS

REN56757

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,629,980 - 64,630,207	UniSTS	GRCh37
Build 36	11	64,386,556 - 64,386,783	RGD	NCBI36
Celera	11	61,956,048 - 61,956,275	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,956,959 - 60,957,186	UniSTS

REN56758

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,630,197 - 64,630,467	UniSTS	GRCh37
Build 36	11	64,386,773 - 64,387,043	RGD	NCBI36
Celera	11	61,956,265 - 61,956,535	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,957,176 - 60,957,446	UniSTS

REN56759

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,630,459 - 64,630,685	UniSTS	GRCh37
Build 36	11	64,387,035 - 64,387,261	RGD	NCBI36
Celera	11	61,956,527 - 61,956,753	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,957,438 - 60,957,664	UniSTS

REN56760

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,630,666 - 64,630,932	UniSTS	GRCh37
Build 36	11	64,387,242 - 64,387,508	RGD	NCBI36
Celera	11	61,956,734 - 61,957,000	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,957,645 - 60,957,911	UniSTS

REN56761

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,630,914 - 64,631,162	UniSTS	GRCh37
Build 36	11	64,387,490 - 64,387,738	RGD	NCBI36
Celera	11	61,956,982 - 61,957,230	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,957,893 - 60,958,141	UniSTS

REN56762

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,145 - 64,631,410	UniSTS	GRCh37
Build 36	11	64,387,721 - 64,387,986	RGD	NCBI36
Celera	11	61,957,213 - 61,957,478	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,124 - 60,958,389	UniSTS

REN56763

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,392 - 64,631,630	UniSTS	GRCh37
Build 36	11	64,387,968 - 64,388,206	RGD	NCBI36
Celera	11	61,957,460 - 61,957,698	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,371 - 60,958,609	UniSTS

REN56764

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,599 - 64,631,848	UniSTS	GRCh37
Build 36	11	64,388,175 - 64,388,424	RGD	NCBI36
Celera	11	61,957,667 - 61,957,916	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,578 - 60,958,827	UniSTS

REN56765

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,821 - 64,632,068	UniSTS	GRCh37
Build 36	11	64,388,397 - 64,388,644	RGD	NCBI36
Celera	11	61,957,889 - 61,958,136	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,800 - 60,959,047	UniSTS

REN56766

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,065 - 64,632,297	UniSTS	GRCh37
Build 36	11	64,388,641 - 64,388,873	RGD	NCBI36
Celera	11	61,958,133 - 61,958,365	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,044 - 60,959,276	UniSTS

REN56767

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,277 - 64,632,539	UniSTS	GRCh37
Build 36	11	64,388,853 - 64,389,115	RGD	NCBI36
Celera	11	61,958,345 - 61,958,607	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,256 - 60,959,518	UniSTS

REN56768

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,519 - 64,632,768	UniSTS	GRCh37
Build 36	11	64,389,095 - 64,389,344	RGD	NCBI36
Celera	11	61,958,587 - 61,958,836	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,498 - 60,959,747	UniSTS

REN56769

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,746 - 64,633,014	UniSTS	GRCh37
Build 36	11	64,389,322 - 64,389,590	RGD	NCBI36
Celera	11	61,958,814 - 61,959,082	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,725 - 60,959,993	UniSTS

REN56770

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,632,966 - 64,633,204	UniSTS	GRCh37
Build 36	11	64,389,542 - 64,389,780	RGD	NCBI36
Celera	11	61,959,034 - 61,959,272	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,959,945 - 60,960,183	UniSTS

REN56771

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,633,182 - 64,633,438	UniSTS	GRCh37
Build 36	11	64,389,758 - 64,390,014	RGD	NCBI36
Celera	11	61,959,250 - 61,959,506	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,960,161 - 60,960,417	UniSTS

REN56772

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,633,408 - 64,633,647	UniSTS	GRCh37
Build 36	11	64,389,984 - 64,390,223	RGD	NCBI36
Celera	11	61,959,476 - 61,959,715	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,960,387 - 60,960,626	UniSTS

REN56773

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,633,625 - 64,633,872	UniSTS	GRCh37
Build 36	11	64,390,201 - 64,390,448	RGD	NCBI36
Celera	11	61,959,693 - 61,959,940	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,960,604 - 60,960,851	UniSTS

REN56774

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,633,843 - 64,634,071	UniSTS	GRCh37
Build 36	11	64,390,419 - 64,390,647	RGD	NCBI36
Celera	11	61,959,911 - 61,960,139	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,960,822 - 60,961,050	UniSTS

REN56775

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,634,044 - 64,634,268	UniSTS	GRCh37
Build 36	11	64,390,620 - 64,390,844	RGD	NCBI36
Celera	11	61,960,112 - 61,960,336	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,961,023 - 60,961,247	UniSTS

REN56776

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,634,235 - 64,634,481	UniSTS	GRCh37
Build 36	11	64,390,811 - 64,391,057	RGD	NCBI36
Celera	11	61,960,303 - 61,960,549	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,961,214 - 60,961,460	UniSTS

REN56777

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,634,384 - 64,634,612	UniSTS	GRCh37
Build 36	11	64,390,960 - 64,391,188	RGD	NCBI36
Celera	11	61,960,452 - 61,960,680	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,961,363 - 60,961,591	UniSTS

REN56778

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,634,563 - 64,634,820	UniSTS	GRCh37
Build 36	11	64,391,139 - 64,391,396	RGD	NCBI36
Celera	11	61,960,631 - 61,960,888	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,961,542 - 60,961,799	UniSTS

REN56779

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,634,921 - 64,635,158	UniSTS	GRCh37
Build 36	11	64,391,497 - 64,391,734	RGD	NCBI36
Celera	11	61,960,989 - 61,961,226	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,961,900 - 60,962,137	UniSTS

REN56780

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,635,138 - 64,635,367	UniSTS	GRCh37
Build 36	11	64,391,714 - 64,391,943	RGD	NCBI36
Celera	11	61,961,206 - 61,961,435	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,117 - 60,962,346	UniSTS

REN56781

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,635,342 - 64,635,577	UniSTS	GRCh37
Build 36	11	64,391,918 - 64,392,153	RGD	NCBI36
Celera	11	61,961,410 - 61,961,645	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,321 - 60,962,556	UniSTS

REN56782

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,635,550 - 64,635,802	UniSTS	GRCh37
Build 36	11	64,392,126 - 64,392,378	RGD	NCBI36
Celera	11	61,961,618 - 61,961,870	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,529 - 60,962,781	UniSTS

REN56783

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,635,781 - 64,636,016	UniSTS	GRCh37
Build 36	11	64,392,357 - 64,392,592	RGD	NCBI36
Celera	11	61,961,849 - 61,962,084	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,760 - 60,962,995	UniSTS

REN56784

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,012 - 64,636,263	UniSTS	GRCh37
Build 36	11	64,392,588 - 64,392,839	RGD	NCBI36
Celera	11	61,962,080 - 61,962,331	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,962,991 - 60,963,242	UniSTS

REN56785

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,255 - 64,636,500	UniSTS	GRCh37
Build 36	11	64,392,831 - 64,393,076	RGD	NCBI36
Celera	11	61,962,323 - 61,962,568	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,963,234 - 60,963,479	UniSTS

REN56786

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,483 - 64,636,726	UniSTS	GRCh37
Build 36	11	64,393,059 - 64,393,302	RGD	NCBI36
Celera	11	61,962,551 - 61,962,794	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,963,462 - 60,963,705	UniSTS

REN56787

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,706 - 64,636,951	UniSTS	GRCh37
Build 36	11	64,393,282 - 64,393,527	RGD	NCBI36
Celera	11	61,962,774 - 61,963,019	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,963,685 - 60,963,930	UniSTS

REN56788

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,636,923 - 64,637,171	UniSTS	GRCh37
Build 36	11	64,393,499 - 64,393,747	RGD	NCBI36
Celera	11	61,962,991 - 61,963,239	RGD
Cytogenetic Map	11	q13	UniSTS

REN56789

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,637,148 - 64,637,411	UniSTS	GRCh37
Build 36	11	64,393,724 - 64,393,987	RGD	NCBI36
Celera	11	61,963,216 - 61,963,479	RGD
Cytogenetic Map	11	q13	UniSTS

REN56790

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,637,391 - 64,637,640	UniSTS	GRCh37
Build 36	11	64,393,967 - 64,394,216	RGD	NCBI36
Celera	11	61,963,459 - 61,963,708	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,964,468 - 60,964,717	UniSTS

REN56791

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,637,618 - 64,637,874	UniSTS	GRCh37
Build 36	11	64,394,194 - 64,394,450	RGD	NCBI36
Celera	11	61,963,686 - 61,963,942	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,964,695 - 60,964,951	UniSTS

REN56792

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,637,873 - 64,638,116	UniSTS	GRCh37
Build 36	11	64,394,449 - 64,394,692	RGD	NCBI36
Celera	11	61,963,941 - 61,964,184	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,964,950 - 60,965,193	UniSTS

REN56793

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,093 - 64,638,353	UniSTS	GRCh37
Build 36	11	64,394,669 - 64,394,929	RGD	NCBI36
Celera	11	61,964,161 - 61,964,421	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,170 - 60,965,430	UniSTS

REN56794

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,327 - 64,638,568	UniSTS	GRCh37
Build 36	11	64,394,903 - 64,395,144	RGD	NCBI36
Celera	11	61,964,395 - 61,964,636	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,404 - 60,965,645	UniSTS

REN56795

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,524 - 64,638,751	UniSTS	GRCh37
Build 36	11	64,395,100 - 64,395,327	RGD	NCBI36
Celera	11	61,964,592 - 61,964,819	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,601 - 60,965,828	UniSTS

REN56796

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,721 - 64,638,968	UniSTS	GRCh37
Build 36	11	64,395,297 - 64,395,544	RGD	NCBI36
Celera	11	61,964,789 - 61,965,036	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,965,798 - 60,966,045	UniSTS

REN56797

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,638,955 - 64,639,203	UniSTS	GRCh37
Build 36	11	64,395,531 - 64,395,779	RGD	NCBI36
Celera	11	61,965,023 - 61,965,271	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,966,032 - 60,966,280	UniSTS

REN56798

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,639,177 - 64,639,441	UniSTS	GRCh37
Build 36	11	64,395,753 - 64,396,017	RGD	NCBI36
Celera	11	61,965,245 - 61,965,509	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,966,254 - 60,966,518	UniSTS

REN56799

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,639,432 - 64,639,689	UniSTS	GRCh37
Build 36	11	64,396,008 - 64,396,265	RGD	NCBI36
Celera	11	61,965,500 - 61,965,757	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,966,509 - 60,966,766	UniSTS

REN56800

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,639,474 - 64,639,698	UniSTS	GRCh37
Build 36	11	64,396,050 - 64,396,274	RGD	NCBI36
Celera	11	61,965,542 - 61,965,766	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,966,551 - 60,966,775	UniSTS

REN56801

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,639,857 - 64,640,104	UniSTS	GRCh37
Build 36	11	64,396,433 - 64,396,680	RGD	NCBI36
Celera	11	61,965,925 - 61,966,172	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,966,934 - 60,967,181	UniSTS

REN56802

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,103 - 64,640,328	UniSTS	GRCh37
Build 36	11	64,396,679 - 64,396,904	RGD	NCBI36
Celera	11	61,966,171 - 61,966,396	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,180 - 60,967,405	UniSTS

REN56803

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,308 - 64,640,548	UniSTS	GRCh37
Build 36	11	64,396,884 - 64,397,124	RGD	NCBI36
Celera	11	61,966,376 - 61,966,616	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,385 - 60,967,625	UniSTS

REN56804

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,509 - 64,640,767	UniSTS	GRCh37
Build 36	11	64,397,085 - 64,397,343	RGD	NCBI36
Celera	11	61,966,577 - 61,966,835	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,586 - 60,967,844	UniSTS

REN56805

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,727 - 64,640,978	UniSTS	GRCh37
Build 36	11	64,397,303 - 64,397,554	RGD	NCBI36
Celera	11	61,966,795 - 61,967,046	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,967,804 - 60,968,055	UniSTS

REN56806

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,640,928 - 64,641,155	UniSTS	GRCh37
Build 36	11	64,397,504 - 64,397,731	RGD	NCBI36
Celera	11	61,966,996 - 61,967,223	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,968,005 - 60,968,232	UniSTS

REN56807

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,641,795 - 64,642,019	UniSTS	GRCh37
Build 36	11	64,398,371 - 64,398,595	RGD	NCBI36
Celera	11	61,967,864 - 61,968,088	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,968,829 - 60,969,053	UniSTS

REN56808

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,642,010 - 64,642,257	UniSTS	GRCh37
Build 36	11	64,398,586 - 64,398,833	RGD	NCBI36
Celera	11	61,968,079 - 61,968,326	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,969,044 - 60,969,291	UniSTS

REN56809

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,642,256 - 64,642,506	UniSTS	GRCh37
Build 36	11	64,398,832 - 64,399,082	RGD	NCBI36
Celera	11	61,968,325 - 61,968,575	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,969,290 - 60,969,540	UniSTS

REN56810

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,642,497 - 64,642,746	UniSTS	GRCh37
Build 36	11	64,399,073 - 64,399,322	RGD	NCBI36
Celera	11	61,968,566 - 61,968,815	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,969,531 - 60,969,780	UniSTS

REN56811

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,642,843 - 64,643,077	UniSTS	GRCh37
Build 36	11	64,399,419 - 64,399,653	RGD	NCBI36
Celera	11	61,968,912 - 61,969,146	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,969,877 - 60,970,111	UniSTS

REN56812

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,064 - 64,643,319	UniSTS	GRCh37
Build 36	11	64,399,640 - 64,399,895	RGD	NCBI36
Celera	11	61,969,133 - 61,969,388	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,970,098 - 60,970,353	UniSTS

REN56813

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,298 - 64,643,546	UniSTS	GRCh37
Build 36	11	64,399,874 - 64,400,122	RGD	NCBI36
Celera	11	61,969,367 - 61,969,615	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,970,332 - 60,970,580	UniSTS

REN56814

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,533 - 64,643,777	UniSTS	GRCh37
Build 36	11	64,400,109 - 64,400,353	RGD	NCBI36
Celera	11	61,969,602 - 61,969,846	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,970,567 - 60,970,811	UniSTS

REN56815

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,749 - 64,643,980	UniSTS	GRCh37
Build 36	11	64,400,325 - 64,400,556	RGD	NCBI36
Celera	11	61,969,818 - 61,970,049	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,970,783 - 60,971,014	UniSTS

REN56816

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,643,977 - 64,644,216	UniSTS	GRCh37
Build 36	11	64,400,553 - 64,400,792	RGD	NCBI36
Celera	11	61,970,046 - 61,970,285	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,011 - 60,971,250	UniSTS

REN56817

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,194 - 64,644,445	UniSTS	GRCh37
Build 36	11	64,400,770 - 64,401,021	RGD	NCBI36
Celera	11	61,970,263 - 61,970,514	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,228 - 60,971,479	UniSTS

REN56818

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,429 - 64,644,668	UniSTS	GRCh37
Build 36	11	64,401,005 - 64,401,244	RGD	NCBI36
Celera	11	61,970,498 - 61,970,737	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,463 - 60,971,702	UniSTS

REN56819

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,660 - 64,644,909	UniSTS	GRCh37
Build 36	11	64,401,236 - 64,401,485	RGD	NCBI36
Celera	11	61,970,729 - 61,970,978	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,694 - 60,971,943	UniSTS

REN56820

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,890 - 64,645,146	UniSTS	GRCh37
Build 36	11	64,401,466 - 64,401,722	RGD	NCBI36
Celera	11	61,970,959 - 61,971,215	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,924 - 60,972,180	UniSTS

REN56821

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,096 - 64,645,354	UniSTS	GRCh37
Build 36	11	64,401,672 - 64,401,930	RGD	NCBI36
Celera	11	61,971,165 - 61,971,423	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,130 - 60,972,388	UniSTS

REN56822

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,333 - 64,645,557	UniSTS	GRCh37
Build 36	11	64,401,909 - 64,402,133	RGD	NCBI36
Celera	11	61,971,402 - 61,971,626	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,367 - 60,972,591	UniSTS

REN56823

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,524 - 64,645,780	UniSTS	GRCh37
Build 36	11	64,402,100 - 64,402,356	RGD	NCBI36
Celera	11	61,971,593 - 61,971,849	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,558 - 60,972,814	UniSTS

REN56824

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,701 - 64,645,941	UniSTS	GRCh37
Build 36	11	64,402,277 - 64,402,517	RGD	NCBI36
Celera	11	61,971,770 - 61,972,010	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,735 - 60,972,975	UniSTS

REN56825

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,645,916 - 64,646,141	UniSTS	GRCh37
Build 36	11	64,402,492 - 64,402,717	RGD	NCBI36
Celera	11	61,971,985 - 61,972,210	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,972,950 - 60,973,175	UniSTS

REN56826

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,118 - 64,646,360	UniSTS	GRCh37
Build 36	11	64,402,694 - 64,402,936	RGD	NCBI36
Celera	11	61,972,187 - 61,972,429	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,152 - 60,973,394	UniSTS

REN56827

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,350 - 64,646,612	UniSTS	GRCh37
Build 36	11	64,402,926 - 64,403,188	RGD	NCBI36
Celera	11	61,972,419 - 61,972,681	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,384 - 60,973,646	UniSTS

REN56828

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,603 - 64,646,854	UniSTS	GRCh37
Build 36	11	64,403,179 - 64,403,430	RGD	NCBI36
Celera	11	61,972,672 - 61,972,923	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,637 - 60,973,888	UniSTS

REN56829

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,646,824 - 64,647,073	UniSTS	GRCh37
Build 36	11	64,403,400 - 64,403,649	RGD	NCBI36
Celera	11	61,972,893 - 61,973,142	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,973,858 - 60,974,107	UniSTS

REN56830

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,647,050 - 64,647,297	UniSTS	GRCh37
Build 36	11	64,403,626 - 64,403,873	RGD	NCBI36
Celera	11	61,973,119 - 61,973,366	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,974,084 - 60,974,331	UniSTS

REN56831

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,647,288 - 64,647,524	UniSTS	GRCh37
Build 36	11	64,403,864 - 64,404,100	RGD	NCBI36
Celera	11	61,973,357 - 61,973,595	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,974,322 - 60,974,560	UniSTS

REN56832

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,647,492 - 64,647,724	UniSTS	GRCh37
Build 36	11	64,404,068 - 64,404,300	RGD	NCBI36
Celera	11	61,973,563 - 61,973,792	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,974,528 - 60,974,757	UniSTS

REN56833

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,647,716 - 64,647,949	UniSTS	GRCh37
Build 36	11	64,404,292 - 64,404,525	RGD	NCBI36
Celera	11	61,973,784 - 61,974,017	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,974,749 - 60,974,982	UniSTS

REN56834

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,647,908 - 64,648,152	UniSTS	GRCh37
Build 36	11	64,404,484 - 64,404,728	RGD	NCBI36
Celera	11	61,973,976 - 61,974,220	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,974,941 - 60,975,185	UniSTS

EHD1_9199

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,556 - 64,622,311	UniSTS	GRCh37
Build 36	11	64,378,132 - 64,378,887	RGD	NCBI36
Celera	11	61,947,721 - 61,948,476	RGD
HuRef	11	60,948,626 - 60,949,381	UniSTS

RH65431

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,644,470 - 64,644,610	UniSTS	GRCh37
Build 36	11	64,401,046 - 64,401,186	RGD	NCBI36
Celera	11	61,970,539 - 61,970,679	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,971,504 - 60,971,644	UniSTS
GeneMap99-GB4 RH Map	11	247.35	UniSTS
NCBI RH Map	11	573.2	UniSTS

G33088

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,631,709 - 64,631,800	UniSTS	GRCh37
Build 36	11	64,388,285 - 64,388,376	RGD	NCBI36
Celera	11	61,957,777 - 61,957,868	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,958,688 - 60,958,779	UniSTS

STS-AA040336

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,621,548 - 64,621,741	UniSTS	GRCh37
Build 36	11	64,378,124 - 64,378,317	RGD	NCBI36
Celera	11	61,947,713 - 61,947,906	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,948,618 - 60,948,811	UniSTS
GeneMap99-GB4 RH Map	11	249.75	UniSTS
NCBI RH Map	11	573.2	UniSTS

STS-W49531

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,253 - 64,620,462	UniSTS	GRCh37
Build 36	11	64,376,829 - 64,377,038	RGD	NCBI36
Celera	11	61,946,418 - 61,946,627	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,323 - 60,947,532	UniSTS
GeneMap99-GB4 RH Map	11	248.1	UniSTS
NCBI RH Map	11	573.2	UniSTS

D11S2921

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	10	q24.33	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	13	q12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	X	p11.4-p11.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	1	q24.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	18	pter-p11.3	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	4	q34.1	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	7	q21.12	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	11	p13-p12	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	5	q12-q13	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	1	p31	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	21	p11.1	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	X	q25-q26.3	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	12	q24.31-q24.32	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	12	p12.2-p11.2	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	18	p11.32	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	9	p24.1-p23	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	7	q31.1-q31.3	UniSTS
Cytogenetic Map	20	q11.21	UniSTS
Cytogenetic Map	20	q12-q13.12	UniSTS
Cytogenetic Map	1	q24-q25.3	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	12	p11.22	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	9	p11	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	15	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	15	q22-qter	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	5	p15.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	19	p13.2-cen	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	9	q33	UniSTS
Cytogenetic Map	1	p36-p35	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	X	q26.2	UniSTS
Cytogenetic Map	8	q13.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	5	p13.1-p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	6	q14.3-q16.1	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	6	q14.3	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	17	q21.1-q21.3	UniSTS
Cytogenetic Map	6	q11.1	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	12	p13.2-p12.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	10	q24-q25	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	14	q11.2-q21	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	5	p14.3	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	9	p13.1	UniSTS
Cytogenetic Map	9	q34.13	UniSTS

RH36905

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	12	q24.11	UniSTS
Cytogenetic Map	1	p21.2	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	1	p12	UniSTS
Cytogenetic Map	10	p12.33	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	18	p11.3-p11.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	3	q27-q28	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	3	q26.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	20	p11.23	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	3	q12.2-q12.3	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	18	q21	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	16	q22	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	11	q12-q13.1	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	9	q21.33	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	18	p11.2	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	9	q31.1	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	1	q25.3	UniSTS
Cytogenetic Map	6	p24-p22.3	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	2	p13	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	10	q21	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	19	p13.13	UniSTS
Cytogenetic Map	10	q26.13	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	10	q24.1	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	14	q22.3	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q12	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	15	q14	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	1	p21.3	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	10	q25-q26	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	7	p14	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS

G32275

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,620,234 - 64,620,346	UniSTS	GRCh37
Celera	11	61,946,399 - 61,946,511	UniSTS
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,947,304 - 60,947,416	UniSTS

REN56733

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	11	q13	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1204	2432	2788	2245	4943	1723	2345	4	622	1947	464	2268	7280	6453	52	3709	847	1732	1612	171

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001282444	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282445	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_006795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF001434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF099011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097842	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK098723	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK124613	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK126581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK299096	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300326	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302930	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312316	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX961798	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY007161	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC036898	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC104799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC104825	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM677440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB093699	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC397966	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC399803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF455404	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000320631 ⟹ ENSP00000320516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,851,642 - 64,878,621 (-)	Ensembl

Ensembl Acc Id:

ENST00000359393 ⟹ ENSP00000352354

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,852,731 - 64,879,677 (-)	Ensembl

Ensembl Acc Id:

ENST00000411683 ⟹ ENSP00000403830

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,874,488 - 64,879,700 (-)	Ensembl

Ensembl Acc Id:

ENST00000421510 ⟹ ENSP00000391429

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,854,612 - 64,877,917 (-)	Ensembl

Ensembl Acc Id:

ENST00000433803 ⟹ ENSP00000404944

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,855,322 - 64,879,699 (-)	Ensembl

Ensembl Acc Id:

ENST00000455148 ⟹ ENSP00000396273

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,859,945 - 64,875,666 (-)	Ensembl

Ensembl Acc Id:

ENST00000457202 ⟹ ENSP00000399022

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,874,478 - 64,888,296 (-)	Ensembl

Ensembl Acc Id:

ENST00000466015

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,859,626 - 64,878,541 (-)	Ensembl

Ensembl Acc Id:

ENST00000484846

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,852,731 - 64,856,663 (-)	Ensembl

Ensembl Acc Id:

ENST00000488711

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,854,292 - 64,855,095 (-)	Ensembl

Ensembl Acc Id:

ENST00000489379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,878,639 - 64,879,681 (-)	Ensembl

Ensembl Acc Id:

ENST00000498472

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,855,052 - 64,860,045 (-)	Ensembl

Ensembl Acc Id:

ENST00000621096 ⟹ ENSP00000479153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,852,727 - 64,879,713 (-)	Ensembl

RefSeq Acc Id:

NM_001282444 ⟹ NP_001269373

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,851,642 - 64,879,693 (-)	NCBI
HuRef	11	60,947,269 - 60,974,219 (-)	NCBI
CHM1_1	11	64,504,019 - 64,530,952 (-)	NCBI
T2T-CHM13v2.0	11	64,844,974 - 64,872,935 (-)	NCBI

Sequence:

show sequence

ACCAGCCTGGACAGCCAAAGGGGTCTGTGTGTGGCCGGGGAGGATGGCGGGGGAGTGAGCCCCA
TGGAACAGCCAGGAACTGATAAAAGATGAGGGGACAAAGACAGTGTGTGTCTGGGAAGCTGGGC
TGAGAGGAGGAGGTGCCGCCGCCTGGGGGTACTCCGATGCTTCCGGGGATTCCGAGCCAGCTGG
AGGACCGCACGTGGCGAACGGCGGGCGCGGCGCGTAGTCAGGGAACCAGGGTGCCTGACTGGGT
GTCTCGTGGAGCCATCCCGCGGGGGTGTGGGGGGGCCACGGTGCCGGAAGGCGCGCGGCCCAGA
GGCCGTCTCCGCCGAACGCCCGCTCCTCGCCTTCCTAACCGCAGCACTTTCGCGAGCCTCCCTA
CGAGGGGCGGGGCGAAACAGCAGCCAGCCCCGTGTCCGGCAGTATGTTCAGCTGGGTCAGCAAG
GATGCCCGCCGCAAGAAGGAGCCGGAGCTCTTCCAGACGGTGGCTGAGGGGCTGCGGCAGCTGT
ACGCGCAGAAGCTGCTACCCCTGGAGGAGCACTACCGCTTCCACGAGTTCCACTCGCCCGCGCT
GGAGGACGCTGACTTCGACAACAAGCCTATGGTGCTCCTCGTGGGGCAGTACAGCACGGGCAAG
ACCACCTTCATCCGACACCTGATCGAGCAGGACTTCCCGGGGATGCGCATCGGGCCCGAGCCCA
CCACCGACTCCTTCATCGCCGTCATGCACGGCCCCACTGAGGGCGTGGTGCCGGGCAACGCGCT
CGTGGTGGACCCGCGGCGCCCCTTCCGCAAGCTCAACGCGTTTGGCAACGCTTTCCTCAACAGG
TTCATGTGTGCCCAGCTGCCCAACCCCGTCCTGGACAGCATCAGCATCATCGACACCCCCGGGA
TCCTGTCTGGAGAGAAGCAGCGGATCAGCAGAGGCTATGACTTTGCAGCCGTCCTGGAGTGGTT
CGCGGAGCGTGTGGACCGCATCATCCTGCTCTTCGACGCCCACAAGCTGGACATCTCCGATGAG
TTCTCGGAAGTGATCAAGGCTCTGAAGAACCATGAGGACAAGATCCGCGTGGTGCTGAACAAGG
CAGACCAGATCGAGACGCAGCAGCTGATGCGGGTGTACGGGGCCCTCATGTGGTCCCTGGGCAA
GATCATCAACACCCCCGAGGTGGTCAGGGTCTACATCGGCTCCTTCTGGTCCCACCCGCTCCTC
ATCCCCGACAACCGCAAGCTCTTTGAGGCCGAGGAGCAGGACCTCTTCAAGGACATCCAGTCAC
TGCCCCGAAACGCCGCCCTCAGGAAGCTCAATGACCTGATCAAGCGGGCACGGCTGGCCAAGGT
TCACGCCTACATCATCAGCTCCCTCAAGAAAGAGATGCCCAATGTCTTTGGTAAAGAGAGCAAA
AAGAAAGAGCTGGTGAACAACCTCGGAGAGATCTACCAGAAGATTGAGCGCGAGCACCAGATCT
CCCCTGGGGACTTCCCGAGCCTCCGCAAGATGCAGGAACTCCTGCAGACCCAGGACTTCAGCAA
GTTCCAGGCGCTGAAGCCCAAGCTGCTGGACACGGTGGATGACATGCTGGCCAACGACATCGCG
CGGCTGATGGTGATGGTGCGGCAGGAGGAGTCCCTGATGCCTTCCCAGGTGGTCAAGGGCGGCG
CCTTTGACGGCACCATGAACGGGCCGTTCGGGCACGGCTACGGCGAGGGGGCCGGCGAGGGCAT
CGACGACGTGGAGTGGGTGGTGGGCAAGGACAAGCCCACCTACGACGAGATCTTCTACACGCTG
TCCCCTGTCAACGGCAAGATCACGGGCGCCAACGCCAAGAAGGAGATGGTGAAGTCCAAGCTCC
CCAACACCGTGCTAGGGAAGATCTGGAAGCTGGCCGACGTGGACAAGGACGGGCTGCTGGACGA
CGAGGAGTTCGCGCTGGCCAACCACCTCATCAAGGTCAAGCTGGAGGGCCACGAGCTGCCCGCC
GACCTGCCCCCGCACCTGGTGCCGCCCTCCAAGCGCAGACATGAGTGATGGCGCCCGGCCCCGC
ACCTGCCATTTGCACGCCCGGCCGGGAGGCAGAGACGGGGGGAGGGGAAGCCTCACCATTTCTC
AAGGTCCATAAAGACTGAGCGGATGTTTCCTCGCCTCTCGAAAAGGAAAACCACCATCTTTCTT
TTAAGGCTGTTCCTGGGCCTGGCGGGGGAGGCAGGGGTGAGAGGATGGAATTGTGTGCACAAGA
ACTGTGGCTATTTTAATATATAACGTTAGAGGCTGCGTTCTTTGTCGCCGCCTCCCCTGTGTGC
CAGCCCTGTGTGCACGGCCTCTGCCCCCCGGCCTTTGCTGTGGCTGGAGCTGGACAGTGCAGCG
ACTGCGACCGTGGGGGAGCCAGGTCGCCCTTTTGGCAGCTGCTAGGCTGAGGCTGCATGGACAG
GAACACCAGGCACCCTCCGTGTGCTTCTGAGCTGAGGTTGCTTCACGGGACCGTGGCTTCCTTC
CTCACCTGGCTCTGCCTCCCCCGTGCTCTCGGGCGAAGTGGGTTCTTGTGCCTTCCCCTCCCGG
GCCCAGGCTCCCCGTGCGCGGGCCCTGCCCTTTCCTCCCGCGCCCCACCGGCTCCGACGCGCAA
CCCCGCTCAGCAGTCACAGAAGCAGGGCCCAGCCACCTTGGTCTTTTTTTGGGAGTTCAGGGGA
GTAGGAGAATGTCTTCCAGAAAAATACATAAGCTAGTTTCTGTTCTGTAAAGTGATATCTTTCA
TACTTGACCAAAGTTCCCAATAACTTCCCAACCACTGTTCAAAAGCTGTGATTTTTGTCTCCCC
TTCCCACCCTCCAGCCAAGGAGCAGCCCTGCCCAGGGGGCATTAGGTGTGGGTACCCGGGGAGC
ACCCCGTTCCTGGACCCCAGTGTTGCATTTCCTGGCTGAGGAAGGGTGGTCATCCCAGCTCCTG
CCCTACCCTCTCACTTAACTGGAGCTTTGGGACGCACCCTCCACAGTGGGAGGTGGTGGTGGGT
GGCGGTGGCGGGGCCTCACGACAGCTTGGTGCTGGTAAGAGGAAGCCCGTGGTTCTGGCTAGGC
TCTCATGTCCAGACAGCGGGGACCAGGGGAAAACCCAGCCCCTTCTGTAATCCCCCTTCATTTC
CTACCTTCCTTCCTCCTCTGTTTAGCAAAGGAGGGCAGCTCACTTGGATGTCCTTACAACGCCC
CTGGCCCCCAGGTTGAGCAATAAGAAACCAGAACCTTGCGGCCCAGTGGCCCGGGCCAGTTCAG
GCCGCCTCCCCCTCCTCTGCCTGGGGCCATTGAGCCCAGCCTCCAGGGCCCGGGCGCGTTTGCA
GGCCAGTGGCCACTGTCCGGGCTGTGATGGCACCAAGGCAGGTGGAGCACCAGGTACCACACAG
CTGGGCTTCCCACCAGGCTTTCCCGCGGGGGTCTCAGGGAGCTTCTCCCCAGCGCTGCTCGGAG
TCTGCAGGAACTGGCCTTGTTCTCCTTAGCCCGTCACTCCATACAGTATTAGGTGAGGATGGAT
GCGGGCGCTGTCCTTGCCGGGAAGTCACTGTTGAAGTTGCAGTGGCTTGTTCACACCTGTGGGA
AGAGAAGTGAAGACTTTCTCCTTGCATTAAAAAGTCTGAACTGTGCGAAAGCTTCGGGTGCTTC
CTTGTCTTTTCCAGGGGCAGCAGTCCTGGGCCATCCTCCCCTGGTGTCTGAGGGGGTGATGCCA
GCAGGGACAGAGTGGCAAGGCAGCCGGGGCAAGGTGACCAACCCTGCCCAGTCCTGCTCTGCTG
GGCAGTAGCTGCCCCCTCCTACTAAGAGGGCCAGGCCTGTAGGGAAAAGGGTTTCTGGGGTGAT
GCCCCCTTCCCTGAGCAAGGTGGGAGCTGAGCAGTTCACTTGGGGTGGGGAGGGGGGAAACAGT
TGGGAGGATGTTGATAGCTGAGGCCTAGGCTGGCACCCCTCAGCCACAGACGGATGAGTGGGCA
CCTGCAGGCCCTCGGCACTGGGTGGCATCAAGTAAACAAGGGTTTCTGGGCTTTGGAGCCAGAC
TGGCTCCTTGCTAGCCCCAAGGACGGTTTAAGTACAGGGAAGCCGGGCCTCTGAAGACAAAGCA
GATAGCCTGTGACAAACATGCAACTAAGGGTGGGGCCAGTCAGGCCCAGGTGATGTCACAGATG
GGGGACTGTTTATACCAGCAGAGGGAAGGGTGACTGATTAGTGACCCTTCATAAAAGGGTGCAG
ACTTGAGGTGCCATGGGTAGAGGCTGCTCCAGCCCCTCTGGCAGAAGGCAGGACAGAAACAAGT
TCCTGAGGGTTTCAGGGACCCAGTTGTGTGCTCCGAGCCTAGCTGGTGTGGTGGTGTCTGGTCC
TATGACCAGCACTTGAGGTGCCAGTGGATGCTTCAGTTGCTGCAGGGCTGGCCGGCCCTCCCTG
CGTCACTCAGCTGCCACCTGTGGGCATTCACCCTGTGCCAGGTGGAGCTGCGCTGTCACGATCT
GAGGAAGTTCATGTTCCCCCATTTCACAGAGGGAGAGTCCGAGACTGAGGACTGCCGAAATAAC
AAAGGTGGTAGAAGCAGATGCAAACCAGGCCGTCCAACTCCAGCGTGCTTTCCATCAGGTTACT
AATCCAAAGCACACACTAAGAGGAAAAAACGGTAGATCCCCCCAACCCCACCCTTAGACTGCAG
CTGTACTCAGGGCTGAGAGACCCACATTAAAGGTTAAATGCTGTCACTCCA

hide sequence

RefSeq Acc Id:

NM_001282445 ⟹ NP_001269374

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,851,642 - 64,879,693 (-)	NCBI
HuRef	11	60,947,269 - 60,974,219 (-)	NCBI
CHM1_1	11	64,504,019 - 64,530,952 (-)	NCBI
T2T-CHM13v2.0	11	64,844,974 - 64,872,935 (-)	NCBI

Sequence:

show sequence

ACCAGCCTGGACAGCCAAAGGGGTCTGTGTGTGGCCGGGGAGGATGGCGGGGGAGTGAGCCCCA
TGGAACAGCCAGGAACTGCAGCCAGCCCCGTGTCCGGCAGTATGTTCAGCTGGGTCAGCAAGGA
TGCCCGCCGCAAGAAGGAGCCGGAGCTCTTCCAGACGGTGGCTGAGGGGCTGCGGCAGCTGTAC
GCGCAGAAGCTGCTACCCCTGGAGGAGCACTACCGCTTCCACGAGTTCCACTCGCCCGCGCTGG
AGGACGCTGACTTCGACAACAAGCCTATGGTGCTCCTCGTGGGGCAGTACAGCACGGGCAAGAC
CACCTTCATCCGACACCTGATCGAGCAGGACTTCCCGGGGATGCGCATCGGGCCCGAGCCCACC
ACCGACTCCTTCATCGCCGTCATGCACGGCCCCACTGAGGGCGTGGTGCCGGGCAACGCGCTCG
TGGTGGACCCGCGGCGCCCCTTCCGCAAGCTCAACGCGTTTGGCAACGCTTTCCTCAACAGGTT
CATGTGTGCCCAGCTGCCCAACCCCGTCCTGGACAGCATCAGCATCATCGACACCCCCGGGATC
CTGTCTGGAGAGAAGCAGCGGATCAGCAGAGGCTATGACTTTGCAGCCGTCCTGGAGTGGTTCG
CGGAGCGTGTGGACCGCATCATCCTGCTCTTCGACGCCCACAAGCTGGACATCTCCGATGAGTT
CTCGGAAGTGATCAAGGCTCTGAAGAACCATGAGGACAAGATCCGCGTGGTGCTGAACAAGGCA
GACCAGATCGAGACGCAGCAGCTGATGCGGGTGTACGGGGCCCTCATGTGGTCCCTGGGCAAGA
TCATCAACACCCCCGAGGTGGTCAGGGTCTACATCGGCTCCTTCTGGTCCCACCCGCTCCTCAT
CCCCGACAACCGCAAGCTCTTTGAGGCCGAGGAGCAGGACCTCTTCAAGGACATCCAGTCACTG
CCCCGAAACGCCGCCCTCAGGAAGCTCAATGACCTGATCAAGCGGGCACGGCTGGCCAAGGTTC
ACGCCTACATCATCAGCTCCCTCAAGAAAGAGATGCCCAATGTCTTTGGTAAAGAGAGCAAAAA
GAAAGAGCTGGTGAACAACCTCGGAGAGATCTACCAGAAGATTGAGCGCGAGCACCAGATCTCC
CCTGGGGACTTCCCGAGCCTCCGCAAGATGCAGGAACTCCTGCAGACCCAGGACTTCAGCAAGT
TCCAGGCGCTGAAGCCCAAGCTGCTGGACACGGTGGATGACATGCTGGCCAACGACATCGCGCG
GCTGATGGTGATGGTGCGGCAGGAGGAGTCCCTGATGCCTTCCCAGGTGGTCAAGGGCGGCGCC
TTTGACGGCACCATGAACGGGCCGTTCGGGCACGGCTACGGCGAGGGGGCCGGCGAGGGCATCG
ACGACGTGGAGTGGGTGGTGGGCAAGGACAAGCCCACCTACGACGAGATCTTCTACACGCTGTC
CCCTGTCAACGGCAAGATCACGGGCGCCAACGCCAAGAAGGAGATGGTGAAGTCCAAGCTCCCC
AACACCGTGCTAGGGAAGATCTGGAAGCTGGCCGACGTGGACAAGGACGGGCTGCTGGACGACG
AGGAGTTCGCGCTGGCCAACCACCTCATCAAGGTCAAGCTGGAGGGCCACGAGCTGCCCGCCGA
CCTGCCCCCGCACCTGGTGCCGCCCTCCAAGCGCAGACATGAGTGATGGCGCCCGGCCCCGCAC
CTGCCATTTGCACGCCCGGCCGGGAGGCAGAGACGGGGGGAGGGGAAGCCTCACCATTTCTCAA
GGTCCATAAAGACTGAGCGGATGTTTCCTCGCCTCTCGAAAAGGAAAACCACCATCTTTCTTTT
AAGGCTGTTCCTGGGCCTGGCGGGGGAGGCAGGGGTGAGAGGATGGAATTGTGTGCACAAGAAC
TGTGGCTATTTTAATATATAACGTTAGAGGCTGCGTTCTTTGTCGCCGCCTCCCCTGTGTGCCA
GCCCTGTGTGCACGGCCTCTGCCCCCCGGCCTTTGCTGTGGCTGGAGCTGGACAGTGCAGCGAC
TGCGACCGTGGGGGAGCCAGGTCGCCCTTTTGGCAGCTGCTAGGCTGAGGCTGCATGGACAGGA
ACACCAGGCACCCTCCGTGTGCTTCTGAGCTGAGGTTGCTTCACGGGACCGTGGCTTCCTTCCT
CACCTGGCTCTGCCTCCCCCGTGCTCTCGGGCGAAGTGGGTTCTTGTGCCTTCCCCTCCCGGGC
CCAGGCTCCCCGTGCGCGGGCCCTGCCCTTTCCTCCCGCGCCCCACCGGCTCCGACGCGCAACC
CCGCTCAGCAGTCACAGAAGCAGGGCCCAGCCACCTTGGTCTTTTTTTGGGAGTTCAGGGGAGT
AGGAGAATGTCTTCCAGAAAAATACATAAGCTAGTTTCTGTTCTGTAAAGTGATATCTTTCATA
CTTGACCAAAGTTCCCAATAACTTCCCAACCACTGTTCAAAAGCTGTGATTTTTGTCTCCCCTT
CCCACCCTCCAGCCAAGGAGCAGCCCTGCCCAGGGGGCATTAGGTGTGGGTACCCGGGGAGCAC
CCCGTTCCTGGACCCCAGTGTTGCATTTCCTGGCTGAGGAAGGGTGGTCATCCCAGCTCCTGCC
CTACCCTCTCACTTAACTGGAGCTTTGGGACGCACCCTCCACAGTGGGAGGTGGTGGTGGGTGG
CGGTGGCGGGGCCTCACGACAGCTTGGTGCTGGTAAGAGGAAGCCCGTGGTTCTGGCTAGGCTC
TCATGTCCAGACAGCGGGGACCAGGGGAAAACCCAGCCCCTTCTGTAATCCCCCTTCATTTCCT
ACCTTCCTTCCTCCTCTGTTTAGCAAAGGAGGGCAGCTCACTTGGATGTCCTTACAACGCCCCT
GGCCCCCAGGTTGAGCAATAAGAAACCAGAACCTTGCGGCCCAGTGGCCCGGGCCAGTTCAGGC
CGCCTCCCCCTCCTCTGCCTGGGGCCATTGAGCCCAGCCTCCAGGGCCCGGGCGCGTTTGCAGG
CCAGTGGCCACTGTCCGGGCTGTGATGGCACCAAGGCAGGTGGAGCACCAGGTACCACACAGCT
GGGCTTCCCACCAGGCTTTCCCGCGGGGGTCTCAGGGAGCTTCTCCCCAGCGCTGCTCGGAGTC
TGCAGGAACTGGCCTTGTTCTCCTTAGCCCGTCACTCCATACAGTATTAGGTGAGGATGGATGC
GGGCGCTGTCCTTGCCGGGAAGTCACTGTTGAAGTTGCAGTGGCTTGTTCACACCTGTGGGAAG
AGAAGTGAAGACTTTCTCCTTGCATTAAAAAGTCTGAACTGTGCGAAAGCTTCGGGTGCTTCCT
TGTCTTTTCCAGGGGCAGCAGTCCTGGGCCATCCTCCCCTGGTGTCTGAGGGGGTGATGCCAGC
AGGGACAGAGTGGCAAGGCAGCCGGGGCAAGGTGACCAACCCTGCCCAGTCCTGCTCTGCTGGG
CAGTAGCTGCCCCCTCCTACTAAGAGGGCCAGGCCTGTAGGGAAAAGGGTTTCTGGGGTGATGC
CCCCTTCCCTGAGCAAGGTGGGAGCTGAGCAGTTCACTTGGGGTGGGGAGGGGGGAAACAGTTG
GGAGGATGTTGATAGCTGAGGCCTAGGCTGGCACCCCTCAGCCACAGACGGATGAGTGGGCACC
TGCAGGCCCTCGGCACTGGGTGGCATCAAGTAAACAAGGGTTTCTGGGCTTTGGAGCCAGACTG
GCTCCTTGCTAGCCCCAAGGACGGTTTAAGTACAGGGAAGCCGGGCCTCTGAAGACAAAGCAGA
TAGCCTGTGACAAACATGCAACTAAGGGTGGGGCCAGTCAGGCCCAGGTGATGTCACAGATGGG
GGACTGTTTATACCAGCAGAGGGAAGGGTGACTGATTAGTGACCCTTCATAAAAGGGTGCAGAC
TTGAGGTGCCATGGGTAGAGGCTGCTCCAGCCCCTCTGGCAGAAGGCAGGACAGAAACAAGTTC
CTGAGGGTTTCAGGGACCCAGTTGTGTGCTCCGAGCCTAGCTGGTGTGGTGGTGTCTGGTCCTA
TGACCAGCACTTGAGGTGCCAGTGGATGCTTCAGTTGCTGCAGGGCTGGCCGGCCCTCCCTGCG
TCACTCAGCTGCCACCTGTGGGCATTCACCCTGTGCCAGGTGGAGCTGCGCTGTCACGATCTGA
GGAAGTTCATGTTCCCCCATTTCACAGAGGGAGAGTCCGAGACTGAGGACTGCCGAAATAACAA
AGGTGGTAGAAGCAGATGCAAACCAGGCCGTCCAACTCCAGCGTGCTTTCCATCAGGTTACTAA
TCCAAAGCACACACTAAGAGGAAAAAACGGTAGATCCCCCCAACCCCACCCTTAGACTGCAGCT
GTACTCAGGGCTGAGAGACCCACATTAAAGGTTAAATGCTGTCACTCCA

hide sequence

RefSeq Acc Id:

NM_006795 ⟹ NP_006786

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,851,642 - 64,878,621 (-)	NCBI
GRCh37	11	64,620,206 - 64,647,181 (-)	NCBI
Build 36	11	64,376,784 - 64,402,767 (-)	NCBI Archive
HuRef	11	60,947,269 - 60,974,219 (-)	NCBI
CHM1_1	11	64,504,019 - 64,530,007 (-)	NCBI
T2T-CHM13v2.0	11	64,844,974 - 64,871,863 (-)	NCBI

Sequence:

show sequence

ATTCGGCAGAGGGCGCTTCGACGGGCTGGGCTGTGCGCCTGCGCAGTGTGGGTCGCTCCCGATT
CCCTGCCCCGGCCGGCCCCGCCTCGGCTCCGCACCCTCGCCCCGCTCTCAGCCGCCGCTCTGCC
CCGCAGCAGCCAGCCCCGTGTCCGGCAGTATGTTCAGCTGGGTCAGCAAGGATGCCCGCCGCAA
GAAGGAGCCGGAGCTCTTCCAGACGGTGGCTGAGGGGCTGCGGCAGCTGTACGCGCAGAAGCTG
CTACCCCTGGAGGAGCACTACCGCTTCCACGAGTTCCACTCGCCCGCGCTGGAGGACGCTGACT
TCGACAACAAGCCTATGGTGCTCCTCGTGGGGCAGTACAGCACGGGCAAGACCACCTTCATCCG
ACACCTGATCGAGCAGGACTTCCCGGGGATGCGCATCGGGCCCGAGCCCACCACCGACTCCTTC
ATCGCCGTCATGCACGGCCCCACTGAGGGCGTGGTGCCGGGCAACGCGCTCGTGGTGGACCCGC
GGCGCCCCTTCCGCAAGCTCAACGCGTTTGGCAACGCTTTCCTCAACAGGTTCATGTGTGCCCA
GCTGCCCAACCCCGTCCTGGACAGCATCAGCATCATCGACACCCCCGGGATCCTGTCTGGAGAG
AAGCAGCGGATCAGCAGAGGCTATGACTTTGCAGCCGTCCTGGAGTGGTTCGCGGAGCGTGTGG
ACCGCATCATCCTGCTCTTCGACGCCCACAAGCTGGACATCTCCGATGAGTTCTCGGAAGTGAT
CAAGGCTCTGAAGAACCATGAGGACAAGATCCGCGTGGTGCTGAACAAGGCAGACCAGATCGAG
ACGCAGCAGCTGATGCGGGTGTACGGGGCCCTCATGTGGTCCCTGGGCAAGATCATCAACACCC
CCGAGGTGGTCAGGGTCTACATCGGCTCCTTCTGGTCCCACCCGCTCCTCATCCCCGACAACCG
CAAGCTCTTTGAGGCCGAGGAGCAGGACCTCTTCAAGGACATCCAGTCACTGCCCCGAAACGCC
GCCCTCAGGAAGCTCAATGACCTGATCAAGCGGGCACGGCTGGCCAAGGTTCACGCCTACATCA
TCAGCTCCCTCAAGAAAGAGATGCCCAATGTCTTTGGTAAAGAGAGCAAAAAGAAAGAGCTGGT
GAACAACCTCGGAGAGATCTACCAGAAGATTGAGCGCGAGCACCAGATCTCCCCTGGGGACTTC
CCGAGCCTCCGCAAGATGCAGGAACTCCTGCAGACCCAGGACTTCAGCAAGTTCCAGGCGCTGA
AGCCCAAGCTGCTGGACACGGTGGATGACATGCTGGCCAACGACATCGCGCGGCTGATGGTGAT
GGTGCGGCAGGAGGAGTCCCTGATGCCTTCCCAGGTGGTCAAGGGCGGCGCCTTTGACGGCACC
ATGAACGGGCCGTTCGGGCACGGCTACGGCGAGGGGGCCGGCGAGGGCATCGACGACGTGGAGT
GGGTGGTGGGCAAGGACAAGCCCACCTACGACGAGATCTTCTACACGCTGTCCCCTGTCAACGG
CAAGATCACGGGCGCCAACGCCAAGAAGGAGATGGTGAAGTCCAAGCTCCCCAACACCGTGCTA
GGGAAGATCTGGAAGCTGGCCGACGTGGACAAGGACGGGCTGCTGGACGACGAGGAGTTCGCGC
TGGCCAACCACCTCATCAAGGTCAAGCTGGAGGGCCACGAGCTGCCCGCCGACCTGCCCCCGCA
CCTGGTGCCGCCCTCCAAGCGCAGACATGAGTGATGGCGCCCGGCCCCGCACCTGCCATTTGCA
CGCCCGGCCGGGAGGCAGAGACGGGGGGAGGGGAAGCCTCACCATTTCTCAAGGTCCATAAAGA
CTGAGCGGATGTTTCCTCGCCTCTCGAAAAGGAAAACCACCATCTTTCTTTTAAGGCTGTTCCT
GGGCCTGGCGGGGGAGGCAGGGGTGAGAGGATGGAATTGTGTGCACAAGAACTGTGGCTATTTT
AATATATAACGTTAGAGGCTGCGTTCTTTGTCGCCGCCTCCCCTGTGTGCCAGCCCTGTGTGCA
CGGCCTCTGCCCCCCGGCCTTTGCTGTGGCTGGAGCTGGACAGTGCAGCGACTGCGACCGTGGG
GGAGCCAGGTCGCCCTTTTGGCAGCTGCTAGGCTGAGGCTGCATGGACAGGAACACCAGGCACC
CTCCGTGTGCTTCTGAGCTGAGGTTGCTTCACGGGACCGTGGCTTCCTTCCTCACCTGGCTCTG
CCTCCCCCGTGCTCTCGGGCGAAGTGGGTTCTTGTGCCTTCCCCTCCCGGGCCCAGGCTCCCCG
TGCGCGGGCCCTGCCCTTTCCTCCCGCGCCCCACCGGCTCCGACGCGCAACCCCGCTCAGCAGT
CACAGAAGCAGGGCCCAGCCACCTTGGTCTTTTTTTGGGAGTTCAGGGGAGTAGGAGAATGTCT
TCCAGAAAAATACATAAGCTAGTTTCTGTTCTGTAAAGTGATATCTTTCATACTTGACCAAAGT
TCCCAATAACTTCCCAACCACTGTTCAAAAGCTGTGATTTTTGTCTCCCCTTCCCACCCTCCAG
CCAAGGAGCAGCCCTGCCCAGGGGGCATTAGGTGTGGGTACCCGGGGAGCACCCCGTTCCTGGA
CCCCAGTGTTGCATTTCCTGGCTGAGGAAGGGTGGTCATCCCAGCTCCTGCCCTACCCTCTCAC
TTAACTGGAGCTTTGGGACGCACCCTCCACAGTGGGAGGTGGTGGTGGGTGGCGGTGGCGGGGC
CTCACGACAGCTTGGTGCTGGTAAGAGGAAGCCCGTGGTTCTGGCTAGGCTCTCATGTCCAGAC
AGCGGGGACCAGGGGAAAACCCAGCCCCTTCTGTAATCCCCCTTCATTTCCTACCTTCCTTCCT
CCTCTGTTTAGCAAAGGAGGGCAGCTCACTTGGATGTCCTTACAACGCCCCTGGCCCCCAGGTT
GAGCAATAAGAAACCAGAACCTTGCGGCCCAGTGGCCCGGGCCAGTTCAGGCCGCCTCCCCCTC
CTCTGCCTGGGGCCATTGAGCCCAGCCTCCAGGGCCCGGGCGCGTTTGCAGGCCAGTGGCCACT
GTCCGGGCTGTGATGGCACCAAGGCAGGTGGAGCACCAGGTACCACACAGCTGGGCTTCCCACC
AGGCTTTCCCGCGGGGGTCTCAGGGAGCTTCTCCCCAGCGCTGCTCGGAGTCTGCAGGAACTGG
CCTTGTTCTCCTTAGCCCGTCACTCCATACAGTATTAGGTGAGGATGGATGCGGGCGCTGTCCT
TGCCGGGAAGTCACTGTTGAAGTTGCAGTGGCTTGTTCACACCTGTGGGAAGAGAAGTGAAGAC
TTTCTCCTTGCATTAAAAAGTCTGAACTGTGCGAAAGCTTCGGGTGCTTCCTTGTCTTTTCCAG
GGGCAGCAGTCCTGGGCCATCCTCCCCTGGTGTCTGAGGGGGTGATGCCAGCAGGGACAGAGTG
GCAAGGCAGCCGGGGCAAGGTGACCAACCCTGCCCAGTCCTGCTCTGCTGGGCAGTAGCTGCCC
CCTCCTACTAAGAGGGCCAGGCCTGTAGGGAAAAGGGTTTCTGGGGTGATGCCCCCTTCCCTGA
GCAAGGTGGGAGCTGAGCAGTTCACTTGGGGTGGGGAGGGGGGAAACAGTTGGGAGGATGTTGA
TAGCTGAGGCCTAGGCTGGCACCCCTCAGCCACAGACGGATGAGTGGGCACCTGCAGGCCCTCG
GCACTGGGTGGCATCAAGTAAACAAGGGTTTCTGGGCTTTGGAGCCAGACTGGCTCCTTGCTAG
CCCCAAGGACGGTTTAAGTACAGGGAAGCCGGGCCTCTGAAGACAAAGCAGATAGCCTGTGACA
AACATGCAACTAAGGGTGGGGCCAGTCAGGCCCAGGTGATGTCACAGATGGGGGACTGTTTATA
CCAGCAGAGGGAAGGGTGACTGATTAGTGACCCTTCATAAAAGGGTGCAGACTTGAGGTGCCAT
GGGTAGAGGCTGCTCCAGCCCCTCTGGCAGAAGGCAGGACAGAAACAAGTTCCTGAGGGTTTCA
GGGACCCAGTTGTGTGCTCCGAGCCTAGCTGGTGTGGTGGTGTCTGGTCCTATGACCAGCACTT
GAGGTGCCAGTGGATGCTTCAGTTGCTGCAGGGCTGGCCGGCCCTCCCTGCGTCACTCAGCTGC
CACCTGTGGGCATTCACCCTGTGCCAGGTGGAGCTGCGCTGTCACGATCTGAGGAAGTTCATGT
TCCCCCATTTCACAGAGGGAGAGTCCGAGACTGAGGACTGCCGAAATAACAAAGGTGGTAGAAG
CAGATGCAAACCAGGCCGTCCAACTCCAGCGTGCTTTCCATCAGGTTACTAATCCAAAGCACAC
ACTAAGAGGAAAAAACGGTAGATCCCCCCAACCCCACCCTTAGACTGCAGCTGTACTCAGGGCT
GAGAGACCCACATTAAAGGTTAAATGCTGTCACTCCA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001269373	(Get FASTA)	NCBI Sequence Viewer
	NP_001269374	(Get FASTA)	NCBI Sequence Viewer
	NP_006786	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB81204	(Get FASTA)	NCBI Sequence Viewer
	AAD45866	(Get FASTA)	NCBI Sequence Viewer
	AAG02009	(Get FASTA)	NCBI Sequence Viewer
	AAI04800	(Get FASTA)	NCBI Sequence Viewer
	AAI04826	(Get FASTA)	NCBI Sequence Viewer
	BAG35240	(Get FASTA)	NCBI Sequence Viewer
	BAG53542	(Get FASTA)	NCBI Sequence Viewer
	BAG60021	(Get FASTA)	NCBI Sequence Viewer
	BAG61156	(Get FASTA)	NCBI Sequence Viewer
	BAG62076	(Get FASTA)	NCBI Sequence Viewer
	BAG64091	(Get FASTA)	NCBI Sequence Viewer
	CAF06408	(Get FASTA)	NCBI Sequence Viewer
	EAW74317	(Get FASTA)	NCBI Sequence Viewer
	EAW74318	(Get FASTA)	NCBI Sequence Viewer
	EAW74319	(Get FASTA)	NCBI Sequence Viewer
	EAW74320	(Get FASTA)	NCBI Sequence Viewer
	EAW74321	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000320516
	ENSP00000320516.3
	ENSP00000352354
	ENSP00000352354.2
	ENSP00000391429.1
	ENSP00000396273.1
	ENSP00000399022.1
	ENSP00000403830.1
	ENSP00000404944.1
	ENSP00000479153
	ENSP00000479153.1
GenBank Protein	Q9H4M9	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_006786 ⟸ NM_006795
- Peptide Label:	isoform 1
- UniProtKB:	Q2M3Q4 (UniProtKB/Swiss-Prot), O14611 (UniProtKB/Swiss-Prot), Q9UNR3 (UniProtKB/Swiss-Prot), Q9H4M9 (UniProtKB/Swiss-Prot), B2R5U3 (UniProtKB/TrEMBL), B4DTR4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFSWVSKDARRKKEPELFQTVAEGLRQLYAQKLLPLEEHYRFHEFHSPALEDADFDNKPMVLLV GQYSTGKTTFIRHLIEQDFPGMRIGPEPTTDSFIAVMHGPTEGVVPGNALVVDPRRPFRKLNAF GNAFLNRFMCAQLPNPVLDSISIIDTPGILSGEKQRISRGYDFAAVLEWFAERVDRIILLFDAH KLDISDEFSEVIKALKNHEDKIRVVLNKADQIETQQLMRVYGALMWSLGKIINTPEVVRVYIGS FWSHPLLIPDNRKLFEAEEQDLFKDIQSLPRNAALRKLNDLIKRARLAKVHAYIISSLKKEMPN VFGKESKKKELVNNLGEIYQKIEREHQISPGDFPSLRKMQELLQTQDFSKFQALKPKLLDTVDD MLANDIARLMVMVRQEESLMPSQVVKGGAFDGTMNGPFGHGYGEGAGEGIDDVEWVVGKDKPTY DEIFYTLSPVNGKITGANAKKEMVKSKLPNTVLGKIWKLADVDKDGLLDDEEFALANHLIKVKL EGHELPADLPPHLVPPSKRRHE hide sequence

RefSeq Acc Id:	NP_001269374 ⟸ NM_001282445
- Peptide Label:	isoform 2
- UniProtKB:	A0A024R571 (UniProtKB/TrEMBL), B4DTR4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEQPGTAASPVSGSMFSWVSKDARRKKEPELFQTVAEGLRQLYAQKLLPLEEHYRFHEFHSPAL EDADFDNKPMVLLVGQYSTGKTTFIRHLIEQDFPGMRIGPEPTTDSFIAVMHGPTEGVVPGNAL VVDPRRPFRKLNAFGNAFLNRFMCAQLPNPVLDSISIIDTPGILSGEKQRISRGYDFAAVLEWF AERVDRIILLFDAHKLDISDEFSEVIKALKNHEDKIRVVLNKADQIETQQLMRVYGALMWSLGK IINTPEVVRVYIGSFWSHPLLIPDNRKLFEAEEQDLFKDIQSLPRNAALRKLNDLIKRARLAKV HAYIISSLKKEMPNVFGKESKKKELVNNLGEIYQKIEREHQISPGDFPSLRKMQELLQTQDFSK FQALKPKLLDTVDDMLANDIARLMVMVRQEESLMPSQVVKGGAFDGTMNGPFGHGYGEGAGEGI DDVEWVVGKDKPTYDEIFYTLSPVNGKITGANAKKEMVKSKLPNTVLGKIWKLADVDKDGLLDD EEFALANHLIKVKLEGHELPADLPPHLVPPSKRRHE hide sequence

RefSeq Acc Id:	NP_001269373 ⟸ NM_001282444
- Peptide Label:	isoform 1
- UniProtKB:	Q2M3Q4 (UniProtKB/Swiss-Prot), O14611 (UniProtKB/Swiss-Prot), Q9UNR3 (UniProtKB/Swiss-Prot), Q9H4M9 (UniProtKB/Swiss-Prot), B2R5U3 (UniProtKB/TrEMBL), B4DTR4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFSWVSKDARRKKEPELFQTVAEGLRQLYAQKLLPLEEHYRFHEFHSPALEDADFDNKPMVLLV GQYSTGKTTFIRHLIEQDFPGMRIGPEPTTDSFIAVMHGPTEGVVPGNALVVDPRRPFRKLNAF GNAFLNRFMCAQLPNPVLDSISIIDTPGILSGEKQRISRGYDFAAVLEWFAERVDRIILLFDAH KLDISDEFSEVIKALKNHEDKIRVVLNKADQIETQQLMRVYGALMWSLGKIINTPEVVRVYIGS FWSHPLLIPDNRKLFEAEEQDLFKDIQSLPRNAALRKLNDLIKRARLAKVHAYIISSLKKEMPN VFGKESKKKELVNNLGEIYQKIEREHQISPGDFPSLRKMQELLQTQDFSKFQALKPKLLDTVDD MLANDIARLMVMVRQEESLMPSQVVKGGAFDGTMNGPFGHGYGEGAGEGIDDVEWVVGKDKPTY DEIFYTLSPVNGKITGANAKKEMVKSKLPNTVLGKIWKLADVDKDGLLDDEEFALANHLIKVKL EGHELPADLPPHLVPPSKRRHE hide sequence

Ensembl Acc Id:

ENSP00000352354 ⟸ ENST00000359393

Ensembl Acc Id:

ENSP00000479153 ⟸ ENST00000621096

Ensembl Acc Id:

ENSP00000403830 ⟸ ENST00000411683

Ensembl Acc Id:

ENSP00000320516 ⟸ ENST00000320631

Ensembl Acc Id:

ENSP00000396273 ⟸ ENST00000455148

Ensembl Acc Id:

ENSP00000399022 ⟸ ENST00000457202

Ensembl Acc Id:

ENSP00000404944 ⟸ ENST00000433803

Ensembl Acc Id:

ENSP00000391429 ⟸ ENST00000421510

Protein Domains

Dynamin-type G EF-hand EH

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H4M9-F1-model_v2	AlphaFold	Q9H4M9	1-534	view protein structure

Promoters

RGD ID:

6814949

Promoter ID:

HG_MRA:2802

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

AF086188

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,376,801 - 64,377,301 (+)	MPROMDB

RGD ID:

6788731

Promoter ID:

HG_KWN:13274

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000143233, OTTHUMT00000143237, OTTHUMT00000315947, UC001OBT.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,379,101 - 64,381,707 (-)	MPROMDB

RGD ID:

6788732

Promoter ID:

HG_KWN:13275

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000315946

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,383,646 - 64,384,392 (-)	MPROMDB

RGD ID:

6788734

Promoter ID:

HG_KWN:13276

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000315948

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,399,751 - 64,400,657 (-)	MPROMDB

RGD ID:

6788728

Promoter ID:

HG_KWN:13277

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000143229, OTTHUMT00000143236, OTTHUMT00000156126

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,401,936 - 64,403,602 (-)	MPROMDB

RGD ID:

6852378

Promoter ID:

EP73996

Type:

initiation region

Name:

HS_EHD1

Description:

EH-domain containing 1.

SO ACC ID:

SO:0000170

Source:

EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Mammalian gene collection (MGC) full-length cDNA cloning

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,402,658 - 64,402,718	EPD

RGD ID:

6788733

Promoter ID:

HG_KWN:13278

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000359393, OTTHUMT00000143235, OTTHUMT00000315949, OTTHUMT00000315950

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,404,229 - 64,404,729 (-)	MPROMDB

RGD ID:

6788735

Promoter ID:

HG_KWN:13279

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid

Transcripts:

OTTHUMT00000315951

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,411,971 - 64,413,287 (-)	MPROMDB

RGD ID:

7220929

Promoter ID:

EPDNEW_H16210

Type:

initiation region

Name:

EHD1_1

Description:

EH domain containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H16211

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,878,621 - 64,878,681	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:3242	AgrOrtholog
COSMIC	EHD1	COSMIC
Ensembl Genes	ENSG00000110047	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000320631	ENTREZGENE
	ENST00000320631.8	UniProtKB/Swiss-Prot
	ENST00000359393	ENTREZGENE
	ENST00000359393.6	UniProtKB/Swiss-Prot
	ENST00000411683.1	UniProtKB/TrEMBL
	ENST00000421510.5	UniProtKB/TrEMBL
	ENST00000433803.1	UniProtKB/TrEMBL
	ENST00000455148.1	UniProtKB/TrEMBL
	ENST00000457202.1	UniProtKB/TrEMBL
	ENST00000621096	ENTREZGENE
	ENST00000621096.4	UniProtKB/TrEMBL
Gene3D-CATH	1.10.268.20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	3.40.50.300	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF-hand	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000110047	GTEx
HGNC ID	HGNC:3242	ENTREZGENE
Human Proteome Map	EHD1	Human Proteome Map
InterPro	DUF5600	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Dynamin_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF-hand-dom_pair	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF_Hand_1_Ca_BS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF_hand_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EH_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EHD_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_DYNAMIN_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	P-loop_NTPase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	TRAFAC_Dynamin-like_GTPase	UniProtKB/TrEMBL
KEGG Report	hsa:10938	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	10938	ENTREZGENE
OMIM	605888	OMIM
PANTHER	EH DOMAIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EPIDERMAL GROWTH FACTOR RECEPTOR PATHWAY SUBSTRATE CLONE 15, ISOFORM A	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR11216:SF127	UniProtKB/TrEMBL
	SARCALUMENIN	UniProtKB/TrEMBL
	TRANSMEMBRANE GTPASE FZO	UniProtKB/TrEMBL
Pfam	DUF5600	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Dynamin_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF-hand_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EHD_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA27677	PharmGKB
PROSITE	EF_HAND_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF_HAND_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_DYNAMIN_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PS50031	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	SM00027	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF47473	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF52540	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A024R571	ENTREZGENE, UniProtKB/TrEMBL
	B2R5U3	ENTREZGENE, UniProtKB/TrEMBL
	B4DTR4	ENTREZGENE, UniProtKB/TrEMBL
	C9IZH1_HUMAN	UniProtKB/TrEMBL
	C9J2Z4_HUMAN	UniProtKB/TrEMBL
	C9JC03_HUMAN	UniProtKB/TrEMBL
	C9JDQ8_HUMAN	UniProtKB/TrEMBL
	C9JIJ3_HUMAN	UniProtKB/TrEMBL
	EHD1_HUMAN	UniProtKB/Swiss-Prot
	O14611	ENTREZGENE
	Q2M3Q4	ENTREZGENE
	Q9H4M9	ENTREZGENE
	Q9UNR3	ENTREZGENE
UniProt Secondary	O14611	UniProtKB/Swiss-Prot
	Q2M3Q4	UniProtKB/Swiss-Prot
	Q9UNR3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-11-17	EHD1	EH domain containing 1	EHD1	EH-domain containing 1	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar