SF1 (splicing factor 1) - Rat Genome Database

Name: SF1
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: SF1 (splicing factor 1) Homo sapiens

Analyze

Symbol:

SF1

Name:

splicing factor 1

RGD ID:

1346504

HGNC Page

HGNC:12950

Description:

Enables identical protein binding activity. Predicted to be involved in regulation of mRNA splicing, via spliceosome. Predicted to act upstream of or within several processes, including Leydig cell differentiation; male sex determination; and nuclear body organization. Located in U2AF complex and nucleoplasm. Part of spliceosomal complex.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

BBP; D11S636; mammalian branch point-binding protein; MBBP; transcription factor ZFM1; ZCCHC25; ZFM1; zinc finger gene in MEN1 locus; zinc finger protein 162; ZNF162

RGD Orthologs

Alliance Genes

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):	Sf1 (splicing factor 1)	HGNC	EggNOG, Ensembl, HGNC, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Rattus norvegicus (Norway rat):	Sf1 (splicing factor 1)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Sf1 (splicing factor 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	SF1 (splicing factor 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	SF1 (splicing factor 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Sf1 (splicing factor 1)	NCBI	Ortholog
Sus scrofa (pig):	SF1 (splicing factor 1)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	SF1 (splicing factor 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Sf1 (splicing factor 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Nr4a1 (nuclear receptor subfamily 4, group A, member 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Sf1 (splicing factor 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Sf1 (splicing factor 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	sf1 (splicing factor 1)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	MSL5	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	SF1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	sfa-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	sf1.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	sf1	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

NCBI Annotation Information:

Note: SF1 (Gene ID: 7536) and NR5A1 (Gene ID: 2516) share the SF1 symbol/alias in common. SF1 is a widely used alternative name for nuclear receptor subfamily 5 group A member 1 (NR5A1), which can be confused with the official symbol for SF1 (splicing factor 1). [01 Jun 2018]

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,786 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,532,078 - 64,546,014 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	64,288,654 - 64,302,817 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	64,288,653 - 64,302,817	NCBI
Celera	11	61,858,574 - 61,872,815 (-)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,858,921 - 60,873,339 (-)	NCBI		HuRef
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	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)

genetic disease (IAGP)

glycogen storage disease V (IAGP)

high grade glioma (IAGP)

intellectual disability (IAGP)

ischemia (ISO)

leukocyte adhesion deficiency 3 (IAGP)

melanoma (EXP)

Neurodevelopmental Disorders (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (EXP)

(+)-schisandrin B (ISO)

(-)-epigallocatechin 3-gallate (EXP)

1,1,1-Trichloro-2-(o-chlorophenyl)-2-(p-chlorophenyl)ethane (ISO)

1,2-dimethylhydrazine (ISO)

14-Deoxy-11,12-didehydroandrographolide (EXP)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP)

17beta-hydroxy-5alpha-androstan-3-one (EXP)

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

2,4-dinitrotoluene (ISO)

2,6-dinitrotoluene (ISO)

2-methylcholine (EXP)

3,4-methylenedioxymethamphetamine (ISO)

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-sulfonyldiphenol (EXP,ISO)

4-amino-2,6-dinitrotoluene (ISO)

8-Br-cAMP (EXP)

acrolein (EXP)

alpha-pinene (EXP)

ammonium chloride (ISO)

benzatropine (EXP)

benzo[a]pyrene (EXP)

bis(2-chloroethyl) sulfide (EXP)

bis(2-ethylhexyl) phthalate (EXP)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

caffeine (EXP)

carmustine (EXP)

cerium trichloride (ISO)

chromium(6+) (ISO)

cisplatin (EXP)

copper(II) sulfate (EXP)

cortisol (EXP)

coumestrol (EXP)

cypermethrin (ISO)

deoxynivalenol (ISO)

dexamethasone (EXP)

dicrotophos (EXP)

dieldrin (ISO)

dihydroartemisinin (EXP)

doxorubicin (EXP)

elemental selenium (EXP)

Enterolactone (EXP)

enzyme inhibitor (EXP)

epoxiconazole (ISO)

ethanol (ISO)

flutamide (ISO)

FR900359 (EXP)

hydralazine (EXP)

hydrogen peroxide (EXP)

hydroxyflutamide (EXP)

indometacin (EXP)

inulin (ISO)

ivermectin (EXP)

methylparaben (EXP)

mifepristone (EXP)

Monobutylphthalate (ISO)

N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal (ISO)

ozone (EXP)

paracetamol (ISO)

perfluorooctane-1-sulfonic acid (ISO)

potassium chromate (EXP)

selenium atom (EXP)

silicon dioxide (EXP)

Soman (ISO)

temozolomide (EXP)

tert-butyl hydroperoxide (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

triadimefon (EXP)

trichloroethene (ISO)

triptonide (ISO)

troglitazone (ISO)

tungsten (ISO)

valproic acid (EXP,ISO)

vinclozolin (ISO)

vitamin E (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

Leydig cell differentiation (IEA,ISO)

male sex determination (IEA,ISO)

mRNA 3'-splice site recognition (TAS)

mRNA processing (IEA)

mRNA splicing, via spliceosome (IC,IEA,NAS)

negative regulation of DNA-templated transcription (IEA)

negative regulation of smooth muscle cell proliferation (IEA,ISO)

nuclear body organization (IEA,ISO)

regulation of mRNA splicing, via spliceosome (IBA,IEA)

regulation of steroid biosynthetic process (IEA,ISO)

RNA splicing (IEA)

spliceosomal complex assembly (NAS)

Cellular Component

nuclear body (IEA)

nucleoplasm (IDA,TAS)

nucleus (IBA,IEA,NAS)

ribosome (NAS)

spliceosomal complex (IDA,IEA,IPI)

U2AF complex (IPI)

Molecular Function

identical protein binding (IPI)

metal ion binding (IEA)

mRNA binding (IBA,IEA)

pre-mRNA branch point binding (IEA)

protein binding (IPI)

RNA binding (HDA,IEA,TAS)

transcription corepressor activity (TAS)

zinc ion binding (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

spliceosome 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.	OMIM Disease Annotation Pipeline	OMIM Disease Annotation Pipeline
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
3.	The spliceosome: design principles of a dynamic RNP machine.	Wahl MC, etal., Cell. 2009 Feb 20;136(4):701-18. doi: 10.1016/j.cell.2009.02.009.

Additional References at PubMed

PMID:1406644	PMID:7912130	PMID:8752089	PMID:9150140	PMID:9192847	PMID:9506990	PMID:9512519	PMID:9573336	PMID:9660765	PMID:9731529	PMID:9765201	PMID:10449420
PMID:11467860	PMID:11604498	PMID:11691992	PMID:12176931	PMID:12477932	PMID:12718882	PMID:12917325	PMID:15105431	PMID:15302935	PMID:15456888	PMID:15489334	PMID:15647371
PMID:16002533	PMID:16055720	PMID:16189514	PMID:16964243	PMID:17024186	PMID:17081983	PMID:17332742	PMID:17383426	PMID:17589525	PMID:18029348	PMID:18285458	PMID:18305892
PMID:18974054	PMID:19738201	PMID:20133449	PMID:21062807	PMID:21145461	PMID:21146534	PMID:21360626	PMID:21505248	PMID:21768215	PMID:21873635	PMID:22365833	PMID:22412018
PMID:22623428	PMID:22658674	PMID:22681889	PMID:22863883	PMID:22906951	PMID:22939629	PMID:23151878	PMID:23273425	PMID:23275563	PMID:23349634	PMID:23403292	PMID:23414517
PMID:23891004	PMID:24457600	PMID:24711643	PMID:24981860	PMID:25043850	PMID:25145264	PMID:25192599	PMID:25416956	PMID:25505242	PMID:25605964	PMID:25921289	PMID:25959826
PMID:26186194	PMID:26344197	PMID:26420826	PMID:26496610	PMID:26641092	PMID:26816005	PMID:27545878	PMID:27684187	PMID:27926873	PMID:28002734	PMID:28225217	PMID:28302793
PMID:28378594	PMID:28431233	PMID:28514442	PMID:28515276	PMID:28533407	PMID:28712289	PMID:29180619	PMID:29298432	PMID:29395067	PMID:29676528	PMID:29845934	PMID:29961565
PMID:30009671	PMID:30110629	PMID:30209976	PMID:30463901	PMID:30585729	PMID:30737378	PMID:30804502	PMID:30833792	PMID:30890647	PMID:30940648	PMID:30948266	PMID:31010829
PMID:31046837	PMID:31059266	PMID:31091453	PMID:31110137	PMID:31280863	PMID:31324722	PMID:31332168	PMID:31343991	PMID:31478661	PMID:31515488	PMID:31586073	PMID:31992135
PMID:32041737	PMID:32203420	PMID:32296183	PMID:32416067	PMID:32538781	PMID:32665550	PMID:32687490	PMID:32780723	PMID:32807901	PMID:32850835	PMID:32877691	PMID:32963011
PMID:32994395	PMID:33397691	PMID:33916271	PMID:33961781	PMID:34079125	PMID:34133714	PMID:34373451	PMID:34650049	PMID:34795231	PMID:35013218	PMID:35013556	PMID:35031058
PMID:35032548	PMID:35198878	PMID:35256949	PMID:35271311	PMID:35439318	PMID:35446349	PMID:35509820	PMID:35545047	PMID:35563538	PMID:35652658	PMID:35831314	PMID:35850772
PMID:35914814	PMID:35944360	PMID:35987950	PMID:36095012	PMID:36173164	PMID:36215168	PMID:36232890	PMID:36244648	PMID:36373674	PMID:36424410	PMID:36517590	PMID:36526897
PMID:36527092	PMID:37268858	PMID:37689310	PMID:37827155	PMID:37892191	PMID:38228887	PMID:38360978

Genomics

Comparative Map Data

SF1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,786 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,532,078 - 64,546,014 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	64,288,654 - 64,302,817 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	64,288,653 - 64,302,817	NCBI
Celera	11	61,858,574 - 61,872,815 (-)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,858,921 - 60,873,339 (-)	NCBI		HuRef
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI		T2T-CHM13v2.0

Sf1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	19	6,413,952 - 6,428,060 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	19	6,413,720 - 6,428,060 (+)	Ensembl		GRCm39 Ensembl
GRCm38	19	6,363,673 - 6,378,038 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	19	6,363,690 - 6,378,030 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	19	6,363,690 - 6,378,038 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	19	6,364,088 - 6,376,425 (+)	NCBI		MGSCv36	mm8
Celera	19	6,236,708 - 6,251,056 (+)	NCBI		Celera
Cytogenetic Map	19	A	NCBI
cM Map	19	4.48	NCBI

Sf1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	213,090,256 - 213,112,688 (+)	NCBI		GRCr8
mRatBN7.2	1	203,670,016 - 203,683,432 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	203,670,018 - 203,684,330 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	212,018,848 - 212,032,153 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	219,115,356 - 219,128,639 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	211,806,411 - 211,819,694 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	221,735,512 - 221,749,216 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	221,735,517 - 221,749,086 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	228,723,282 - 228,737,009 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	209,146,177 - 209,159,459 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	209,312,189 - 209,313,441 (+)	NCBI
Celera	1	201,203,443 - 201,216,725 (+)	NCBI		Celera
Cytogenetic Map	1	q43	NCBI

Sf1
(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	20,391,722 - 20,551,870 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	20,391,340 - 20,406,555 (+)	NCBI	ChiLan1.0	ChiLan1.0

SF1
(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	65,990,503 - 66,006,673 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	67,033,499 - 67,048,030 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	60,120,126 - 60,134,279 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	63,461,318 - 63,473,350 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	63,461,318 - 63,473,355 (-)	Ensembl	panpan1.1		panPan2

SF1
(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	52,380,058 - 52,393,833 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	52,380,211 - 52,393,048 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	50,987,426 - 51,001,160 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	53,421,292 - 53,435,068 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	53,421,043 - 53,435,063 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	52,516,258 - 52,529,989 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	52,102,165 - 52,115,924 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	52,886,303 - 52,900,036 (+)	NCBI		UU_Cfam_GSD_1.0

Sf1
(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	8,091,417 - 8,104,506 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936599	4,533,795 - 4,546,853 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936599	4,533,664 - 4,546,857 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SF1
(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	7,391,383 - 7,404,948 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	7,391,295 - 7,404,693 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	6,522,689 - 6,537,534 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SF1
(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	9,456,524 - 9,470,920 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	9,456,971 - 9,472,396 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	106,845,714 - 106,860,060 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Sf1
(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	21,606,065 - 21,621,830 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624767	21,606,059 - 21,621,831 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SF1
29 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
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
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_004630.4(SF1):c.1336C>G (p.Pro446Ala)	single nucleotide variant	Inborn genetic diseases [RCV003300049]	Chr11:64767577 [GRCh38] Chr11:64535049 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+349A>G	single nucleotide variant	Inborn genetic diseases [RCV003300168]	Chr11:64778013 [GRCh38] Chr11:64545485 [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
GRCh37/hg19 11q13.1(chr11:64396501-64883447)x3	copy number gain	not provided [RCV000848683]	Chr11:64396501..64883447 [GRCh37] Chr11:11q13.1	uncertain significance
dup(11)(q13.1q13.1)	duplication	Ependymoma [RCV000785872]	Chr11:63533279..65429676 [GRCh37] Chr11:11q13.1	likely pathogenic
GRCh37/hg19 11q13.1(chr11:64474135-64611928)x3	copy number gain	not provided [RCV000848374]	Chr11:64474135..64611928 [GRCh37] Chr11:11q13.1	uncertain significance
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
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
NM_004630.4(SF1):c.221del (p.Pro74fs)	deletion	Neurodevelopmental disorder [RCV001780022]	Chr11:64773445 [GRCh38] Chr11:64540917 [GRCh37] Chr11:11q13.1	likely pathogenic
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
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
NM_004630.4(SF1):c.1364C>T (p.Pro455Leu)	single nucleotide variant	Inborn genetic diseases [RCV002841261]	Chr11:64767230 [GRCh38] Chr11:64534702 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.1045C>T (p.Pro349Ser)	single nucleotide variant	Inborn genetic diseases [RCV002839959]	Chr11:64768129 [GRCh38] Chr11:64535601 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.1115G>T (p.Gly372Val)	single nucleotide variant	Inborn genetic diseases [RCV002779057]	Chr11:64767798 [GRCh38] Chr11:64535270 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+141G>A	single nucleotide variant	Inborn genetic diseases [RCV002684358]	Chr11:64778221 [GRCh38] Chr11:64545693 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.*348T>C	single nucleotide variant	Inborn genetic diseases [RCV002728109]	Chr11:64765470 [GRCh38] Chr11:64532942 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.*339T>A	single nucleotide variant	Inborn genetic diseases [RCV002778330]	Chr11:64765479 [GRCh38] Chr11:64532951 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+325C>T	single nucleotide variant	Inborn genetic diseases [RCV002839995]	Chr11:64778037 [GRCh38] Chr11:64545509 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+259C>T	single nucleotide variant	Inborn genetic diseases [RCV002732871]	Chr11:64778103 [GRCh38] Chr11:64545575 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+256A>G	single nucleotide variant	Inborn genetic diseases [RCV002733852]	Chr11:64778106 [GRCh38] Chr11:64545578 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.*332A>G	single nucleotide variant	Inborn genetic diseases [RCV002845863]	Chr11:64765486 [GRCh38] Chr11:64532958 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+196C>T	single nucleotide variant	Inborn genetic diseases [RCV002823503]	Chr11:64778166 [GRCh38] Chr11:64545638 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+316C>G	single nucleotide variant	Inborn genetic diseases [RCV002823531]	Chr11:64778046 [GRCh38] Chr11:64545518 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+286C>T	single nucleotide variant	Inborn genetic diseases [RCV002662130]	Chr11:64778076 [GRCh38] Chr11:64545548 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.18C>G (p.Asn6Lys)	single nucleotide variant	Inborn genetic diseases [RCV002738325]	Chr11:64778375 [GRCh38] Chr11:64545847 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+277C>T	single nucleotide variant	Inborn genetic diseases [RCV002743126]	Chr11:64778085 [GRCh38] Chr11:64545557 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+265C>T	single nucleotide variant	Inborn genetic diseases [RCV002789831]	Chr11:64778097 [GRCh38] Chr11:64545569 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.923G>A (p.Arg308Gln)	single nucleotide variant	Inborn genetic diseases [RCV002875028]	Chr11:64768251 [GRCh38] Chr11:64535723 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.1186A>G (p.Ser396Gly)	single nucleotide variant	Inborn genetic diseases [RCV002708948]	Chr11:64767727 [GRCh38] Chr11:64535199 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+285C>T	single nucleotide variant	Inborn genetic diseases [RCV003004515]	Chr11:64778077 [GRCh38] Chr11:64545549 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+139G>C	single nucleotide variant	Inborn genetic diseases [RCV002940422]	Chr11:64778223 [GRCh38] Chr11:64545695 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+240T>G	single nucleotide variant	Inborn genetic diseases [RCV003211407]	Chr11:64778122 [GRCh38] Chr11:64545594 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+339A>C	single nucleotide variant	Inborn genetic diseases [RCV003302444]	Chr11:64778023 [GRCh38] Chr11:64545495 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+358C>T	single nucleotide variant	Inborn genetic diseases [RCV003180792]	Chr11:64778004 [GRCh38] Chr11:64545476 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.18C>A (p.Asn6Lys)	single nucleotide variant	Inborn genetic diseases [RCV003188768]	Chr11:64778375 [GRCh38] Chr11:64545847 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.1439C>T (p.Pro480Leu)	single nucleotide variant	Inborn genetic diseases [RCV003287585]	Chr11:64767043 [GRCh38] Chr11:64534515 [GRCh37] Chr11:11q13.1	uncertain significance
NM_004630.4(SF1):c.31+54G>C	single nucleotide variant	Inborn genetic diseases [RCV003348175]	Chr11:64778308 [GRCh38] Chr11:64545780 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q13.1(chr11:63643711-64533636)x1	copy number loss	not provided [RCV003483125]	Chr11:63643711..64533636 [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:	6492
Count of miRNA genes:	1146
Interacting mature miRNAs:	1442
Transcripts:	ENST00000227503, ENST00000334944, ENST00000377387, ENST00000377390, ENST00000377394, ENST00000413725, ENST00000413951, ENST00000422298, ENST00000432725, ENST00000433274, ENST00000443908, ENST00000448404, ENST00000463343, ENST00000472725, ENST00000477596, ENST00000482693, ENST00000486867, ENST00000486960, ENST00000489544, ENST00000496969
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.

Markers in Region

D11S4350

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,209 - 64,532,300	UniSTS	GRCh37
Build 36	11	64,288,785 - 64,288,876	RGD	NCBI36
Celera	11	61,858,707 - 61,858,798	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,054 - 60,859,145	UniSTS
TNG Radiation Hybrid Map	11	28572.0	UniSTS
Stanford-G3 RH Map	11	2805.0	UniSTS
GeneMap99-G3 RH Map	11	2805.0	UniSTS

RH91433

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,140 - 64,532,300	UniSTS	GRCh37
Build 36	11	64,288,716 - 64,288,876	RGD	NCBI36
Celera	11	61,858,638 - 61,858,798	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,858,985 - 60,859,145	UniSTS
GeneMap99-GB4 RH Map	11	238.23	UniSTS

SHGC-35223

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,138 - 64,539,267	UniSTS	GRCh37
Build 36	11	64,295,714 - 64,295,843	RGD	NCBI36
Celera	11	61,865,636 - 61,865,765	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,160 - 60,866,289	UniSTS
Stanford-G3 RH Map	11	2816.0	UniSTS
GeneMap99-GB4 RH Map	11	247.67	UniSTS
Whitehead-RH Map	11	335.8	UniSTS
NCBI RH Map	11	573.2	UniSTS
GeneMap99-G3 RH Map	11	2816.0	UniSTS

STS-D26120

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,290 - 64,532,509	UniSTS	GRCh37
Build 36	11	64,288,866 - 64,289,085	RGD	NCBI36
Celera	11	61,858,788 - 61,859,007	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,135 - 60,859,354	UniSTS
GeneMap99-GB4 RH Map	11	236.71	UniSTS
NCBI RH Map	11	573.2	UniSTS

ECD00563

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,245 - 64,535,144	UniSTS	GRCh37
Build 36	11	64,290,821 - 64,291,720	RGD	NCBI36
Celera	11	61,860,743 - 61,861,642	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,267 - 60,862,166	UniSTS

ECD00564

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,405 - 64,544,304	UniSTS	GRCh37
Build 36	11	64,299,981 - 64,300,880	RGD	NCBI36
Celera	11	61,869,903 - 61,870,803	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,427 - 60,871,327	UniSTS

ECD00610

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,079 - 64,536,976	UniSTS	GRCh37
Build 36	11	64,292,655 - 64,293,552	RGD	NCBI36
Celera	11	61,862,577 - 61,863,474	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,863,101 - 60,863,998	UniSTS

ECD00773

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,037 - 64,537,927	UniSTS	GRCh37
Build 36	11	64,293,613 - 64,294,503	RGD	NCBI36
Celera	11	61,863,535 - 61,864,425	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,059 - 60,864,949	UniSTS

ECD00774

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,870 - 64,539,760	UniSTS	GRCh37
Build 36	11	64,295,446 - 64,296,336	RGD	NCBI36
Celera	11	61,865,368 - 61,866,258	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,892 - 60,866,782	UniSTS

ECD01224

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,542,481 - 64,543,353	UniSTS	GRCh37
Build 36	11	64,299,057 - 64,299,929	RGD	NCBI36
Celera	11	61,868,979 - 61,869,851	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,869,503 - 60,870,375	UniSTS

ECD02055

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,380 - 64,533,223	UniSTS	GRCh37
Build 36	11	64,288,956 - 64,289,799	RGD	NCBI36
Celera	11	61,858,878 - 61,859,721	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,225 - 60,860,068	UniSTS

ECD02214

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,167 - 64,536,004	UniSTS	GRCh37
Build 36	11	64,291,743 - 64,292,580	RGD	NCBI36
Celera	11	61,861,665 - 61,862,502	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,189 - 60,863,026	UniSTS

ECD02238

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,359 - 64,534,195	UniSTS	GRCh37
Build 36	11	64,289,935 - 64,290,771	RGD	NCBI36
Celera	11	61,859,857 - 61,860,693	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,860,204 - 60,861,217	UniSTS

ECD02969

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,374 - 64,545,184	UniSTS	GRCh37
Build 36	11	64,300,950 - 64,301,760	RGD	NCBI36
Celera	11	61,870,873 - 61,871,683	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,871,397 - 60,872,207	UniSTS

ECD03799

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,985 - 64,538,768	UniSTS	GRCh37
Build 36	11	64,294,561 - 64,295,344	RGD	NCBI36
Celera	11	61,864,483 - 61,865,266	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,007 - 60,865,790	UniSTS

ECD04767

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,612 - 64,541,366	UniSTS	GRCh37
Build 36	11	64,297,188 - 64,297,942	RGD	NCBI36
Celera	11	61,867,110 - 61,867,864	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,867,634 - 60,868,388	UniSTS

ECD05379

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,829 - 64,540,566	UniSTS	GRCh37
Build 36	11	64,296,405 - 64,297,142	RGD	NCBI36
Celera	11	61,866,327 - 61,867,064	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,851 - 60,867,588	UniSTS

ECD05866

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,371 - 64,542,095	UniSTS	GRCh37
Build 36	11	64,297,947 - 64,298,671	RGD	NCBI36
Celera	11	61,867,869 - 61,868,593	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,393 - 60,869,117	UniSTS

ECD10230

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,088 - 64,546,695	UniSTS	GRCh37
Build 36	11	64,302,664 - 64,303,271	RGD	NCBI36
Celera	11	61,872,587 - 61,873,194	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,873,111 - 60,873,718	UniSTS

ECD23065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,547,613 - 64,547,812	UniSTS	GRCh37
Build 36	11	64,304,189 - 64,304,388	RGD	NCBI36
Celera	11	61,874,113 - 61,874,312	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,874,639 - 60,874,838	UniSTS

REN56360

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,531,711 - 64,531,945	UniSTS	GRCh37
Build 36	11	64,288,287 - 64,288,521	RGD	NCBI36
Celera	11	61,858,209 - 61,858,443	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,858,556 - 60,858,790	UniSTS

REN56361

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,531,921 - 64,532,145	UniSTS	GRCh37
Build 36	11	64,288,497 - 64,288,721	RGD	NCBI36
Celera	11	61,858,419 - 61,858,643	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,858,766 - 60,858,990	UniSTS

REN56362

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,120 - 64,532,369	UniSTS	GRCh37
Build 36	11	64,288,696 - 64,288,945	RGD	NCBI36
Celera	11	61,858,618 - 61,858,867	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,858,965 - 60,859,214	UniSTS

REN56363

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,346 - 64,532,576	UniSTS	GRCh37
Build 36	11	64,288,922 - 64,289,152	RGD	NCBI36
Celera	11	61,858,844 - 61,859,074	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,191 - 60,859,421	UniSTS

REN56364

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,554 - 64,532,778	UniSTS	GRCh37
Build 36	11	64,289,130 - 64,289,354	RGD	NCBI36
Celera	11	61,859,052 - 61,859,276	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,399 - 60,859,623	UniSTS

REN56365

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,532,761 - 64,533,019	UniSTS	GRCh37
Build 36	11	64,289,337 - 64,289,595	RGD	NCBI36
Celera	11	61,859,259 - 61,859,517	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,606 - 60,859,864	UniSTS

REN56366

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,016 - 64,533,241	UniSTS	GRCh37
Build 36	11	64,289,592 - 64,289,817	RGD	NCBI36
Celera	11	61,859,514 - 61,859,739	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,859,861 - 60,860,086	UniSTS

REN56367

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,169 - 64,533,396	UniSTS	GRCh37
Build 36	11	64,289,745 - 64,289,972	RGD	NCBI36
Celera	11	61,859,667 - 61,859,894	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,860,014 - 60,860,241	UniSTS

REN56368

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,368 - 64,533,629	UniSTS	GRCh37
Build 36	11	64,289,944 - 64,290,205	RGD	NCBI36
Celera	11	61,859,866 - 61,860,127	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,860,213 - 60,860,474	UniSTS

REN56369

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,621 - 64,533,858	UniSTS	GRCh37
Build 36	11	64,290,197 - 64,290,434	RGD	NCBI36
Celera	11	61,860,119 - 61,860,356	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,860,466 - 60,860,880	UniSTS

REN56370

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,827 - 64,534,061	UniSTS	GRCh37
Build 36	11	64,290,403 - 64,290,637	RGD	NCBI36
Celera	11	61,860,325 - 61,860,559	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,860,849 - 60,861,083	UniSTS

REN56371

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,058 - 64,534,317	UniSTS	GRCh37
Build 36	11	64,290,634 - 64,290,893	RGD	NCBI36
Celera	11	61,860,556 - 61,860,815	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,080 - 60,861,339	UniSTS

REN56372

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,294 - 64,534,540	UniSTS	GRCh37
Build 36	11	64,290,870 - 64,291,116	RGD	NCBI36
Celera	11	61,860,792 - 61,861,038	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,316 - 60,861,562	UniSTS

REN56373

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,520 - 64,534,769	UniSTS	GRCh37
Build 36	11	64,291,096 - 64,291,345	RGD	NCBI36
Celera	11	61,861,018 - 61,861,267	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,542 - 60,861,791	UniSTS

REN56374

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,747 - 64,535,003	UniSTS	GRCh37
Build 36	11	64,291,323 - 64,291,579	RGD	NCBI36
Celera	11	61,861,245 - 61,861,501	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,769 - 60,862,025	UniSTS

REN56375

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,953 - 64,535,202	UniSTS	GRCh37
Build 36	11	64,291,529 - 64,291,778	RGD	NCBI36
Celera	11	61,861,451 - 61,861,700	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,861,975 - 60,862,224	UniSTS

REN56376

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,181 - 64,535,421	UniSTS	GRCh37
Build 36	11	64,291,757 - 64,291,997	RGD	NCBI36
Celera	11	61,861,679 - 61,861,919	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,203 - 60,862,443	UniSTS

REN56377

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,411 - 64,535,681	UniSTS	GRCh37
Build 36	11	64,291,987 - 64,292,257	RGD	NCBI36
Celera	11	61,861,909 - 61,862,179	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,433 - 60,862,703	UniSTS

REN56378

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,671 - 64,535,903	UniSTS	GRCh37
Build 36	11	64,292,247 - 64,292,479	RGD	NCBI36
Celera	11	61,862,169 - 61,862,401	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,693 - 60,862,925	UniSTS

REN56379

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,901 - 64,536,140	UniSTS	GRCh37
Build 36	11	64,292,477 - 64,292,716	RGD	NCBI36
Celera	11	61,862,399 - 61,862,638	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,923 - 60,863,162	UniSTS

REN56380

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,136 - 64,536,367	UniSTS	GRCh37
Build 36	11	64,292,712 - 64,292,943	RGD	NCBI36
Celera	11	61,862,634 - 61,862,865	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,863,158 - 60,863,389	UniSTS

REN56381

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,351 - 64,536,601	UniSTS	GRCh37
Build 36	11	64,292,927 - 64,293,177	RGD	NCBI36
Celera	11	61,862,849 - 61,863,099	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,863,373 - 60,863,623	UniSTS

REN56382

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,556 - 64,536,807	UniSTS	GRCh37
Build 36	11	64,293,132 - 64,293,383	RGD	NCBI36
Celera	11	61,863,054 - 61,863,305	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,863,578 - 60,863,829	UniSTS

REN56383

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,784 - 64,537,023	UniSTS	GRCh37
Build 36	11	64,293,360 - 64,293,599	RGD	NCBI36
Celera	11	61,863,282 - 61,863,521	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,863,806 - 60,864,045	UniSTS

REN56384

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,536,997 - 64,537,246	UniSTS	GRCh37
Build 36	11	64,293,573 - 64,293,822	RGD	NCBI36
Celera	11	61,863,495 - 61,863,744	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,019 - 60,864,268	UniSTS

REN56385

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,223 - 64,537,482	UniSTS	GRCh37
Build 36	11	64,293,799 - 64,294,058	RGD	NCBI36
Celera	11	61,863,721 - 61,863,980	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,245 - 60,864,504	UniSTS

REN56386

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,467 - 64,537,711	UniSTS	GRCh37
Build 36	11	64,294,043 - 64,294,287	RGD	NCBI36
Celera	11	61,863,965 - 61,864,209	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,489 - 60,864,733	UniSTS

REN56387

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,678 - 64,537,927	UniSTS	GRCh37
Build 36	11	64,294,254 - 64,294,503	RGD	NCBI36
Celera	11	61,864,176 - 61,864,425	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,700 - 60,864,949	UniSTS

REN56388

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,924 - 64,538,165	UniSTS	GRCh37
Build 36	11	64,294,500 - 64,294,741	RGD	NCBI36
Celera	11	61,864,422 - 61,864,663	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,864,946 - 60,865,187	UniSTS

REN56389

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,142 - 64,538,403	UniSTS	GRCh37
Build 36	11	64,294,718 - 64,294,979	RGD	NCBI36
Celera	11	61,864,640 - 61,864,901	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,164 - 60,865,425	UniSTS

REN56390

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,382 - 64,538,642	UniSTS	GRCh37
Build 36	11	64,294,958 - 64,295,218	RGD	NCBI36
Celera	11	61,864,880 - 61,865,140	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,404 - 60,865,664	UniSTS

REN56391

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,626 - 64,538,874	UniSTS	GRCh37
Build 36	11	64,295,202 - 64,295,450	RGD	NCBI36
Celera	11	61,865,124 - 61,865,372	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,648 - 60,865,896	UniSTS

REN56392

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,849 - 64,539,098	UniSTS	GRCh37
Build 36	11	64,295,425 - 64,295,674	RGD	NCBI36
Celera	11	61,865,347 - 61,865,596	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,865,871 - 60,866,120	UniSTS

REN56393

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,087 - 64,539,326	UniSTS	GRCh37
Build 36	11	64,295,663 - 64,295,902	RGD	NCBI36
Celera	11	61,865,585 - 61,865,824	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,109 - 60,866,348	UniSTS

REN56394

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,315 - 64,539,558	UniSTS	GRCh37
Build 36	11	64,295,891 - 64,296,134	RGD	NCBI36
Celera	11	61,865,813 - 61,866,056	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,337 - 60,866,580	UniSTS

REN56395

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,554 - 64,539,781	UniSTS	GRCh37
Build 36	11	64,296,130 - 64,296,357	RGD	NCBI36
Celera	11	61,866,052 - 61,866,279	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,576 - 60,866,803	UniSTS

REN56396

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,751 - 64,539,998	UniSTS	GRCh37
Build 36	11	64,296,327 - 64,296,574	RGD	NCBI36
Celera	11	61,866,249 - 61,866,496	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,773 - 60,867,020	UniSTS

REN56397

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,975 - 64,540,233	UniSTS	GRCh37
Build 36	11	64,296,551 - 64,296,809	RGD	NCBI36
Celera	11	61,866,473 - 61,866,731	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,866,997 - 60,867,255	UniSTS

REN56398

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,208 - 64,540,454	UniSTS	GRCh37
Build 36	11	64,296,784 - 64,297,030	RGD	NCBI36
Celera	11	61,866,706 - 61,866,952	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,867,230 - 60,867,476	UniSTS

REN56399

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,449 - 64,540,687	UniSTS	GRCh37
Build 36	11	64,297,025 - 64,297,263	RGD	NCBI36
Celera	11	61,866,947 - 61,867,185	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,867,471 - 60,867,709	UniSTS

REN56400

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,658 - 64,540,908	UniSTS	GRCh37
Build 36	11	64,297,234 - 64,297,484	RGD	NCBI36
Celera	11	61,867,156 - 61,867,406	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,867,680 - 60,867,930	UniSTS

REN56401

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,899 - 64,541,156	UniSTS	GRCh37
Build 36	11	64,297,475 - 64,297,732	RGD	NCBI36
Celera	11	61,867,397 - 61,867,654	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,867,921 - 60,868,178	UniSTS

REN56402

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,133 - 64,541,373	UniSTS	GRCh37
Build 36	11	64,297,709 - 64,297,949	RGD	NCBI36
Celera	11	61,867,631 - 61,867,871	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,155 - 60,868,395	UniSTS

REN56403

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,348 - 64,541,603	UniSTS	GRCh37
Build 36	11	64,297,924 - 64,298,179	RGD	NCBI36
Celera	11	61,867,846 - 61,868,101	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,370 - 60,868,625	UniSTS

REN56404

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,593 - 64,541,836	UniSTS	GRCh37
Build 36	11	64,298,169 - 64,298,412	RGD	NCBI36
Celera	11	61,868,091 - 61,868,334	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,615 - 60,868,858	UniSTS

REN56405

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,812 - 64,542,044	UniSTS	GRCh37
Build 36	11	64,298,388 - 64,298,620	RGD	NCBI36
Celera	11	61,868,310 - 61,868,542	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,834 - 60,869,066	UniSTS

REN56406

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,922 - 64,542,155	UniSTS	GRCh37
Build 36	11	64,298,498 - 64,298,731	RGD	NCBI36
Celera	11	61,868,420 - 61,868,653	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,868,944 - 60,869,177	UniSTS

REN56407

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,542,461 - 64,542,686	UniSTS	GRCh37
Build 36	11	64,299,037 - 64,299,262	RGD	NCBI36
Celera	11	61,868,959 - 61,869,184	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,869,483 - 60,869,708	UniSTS

REN56408

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,542,682 - 64,542,935	UniSTS	GRCh37
Build 36	11	64,299,258 - 64,299,511	RGD	NCBI36
Celera	11	61,869,180 - 61,869,433	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,869,704 - 60,869,957	UniSTS

REN56409

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,542,907 - 64,543,138	UniSTS	GRCh37
Build 36	11	64,299,483 - 64,299,714	RGD	NCBI36
Celera	11	61,869,405 - 61,869,636	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,869,929 - 60,870,160	UniSTS

REN56410

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,115 - 64,543,364	UniSTS	GRCh37
Build 36	11	64,299,691 - 64,299,940	RGD	NCBI36
Celera	11	61,869,613 - 61,869,862	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,137 - 60,870,386	UniSTS

REN56411

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,335 - 64,543,602	UniSTS	GRCh37
Build 36	11	64,299,911 - 64,300,178	RGD	NCBI36
Celera	11	61,869,833 - 61,870,101	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,357 - 60,870,625	UniSTS

REN56412

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,586 - 64,543,815	UniSTS	GRCh37
Build 36	11	64,300,162 - 64,300,391	RGD	NCBI36
Celera	11	61,870,085 - 61,870,314	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,609 - 60,870,838	UniSTS

REN56413

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,780 - 64,544,051	UniSTS	GRCh37
Build 36	11	64,300,356 - 64,300,627	RGD	NCBI36
Celera	11	61,870,279 - 61,870,550	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,803 - 60,871,074	UniSTS

REN56414

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,039 - 64,544,294	UniSTS	GRCh37
Build 36	11	64,300,615 - 64,300,870	RGD	NCBI36
Celera	11	61,870,538 - 61,870,793	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,871,062 - 60,871,317	UniSTS

REN56415

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,280 - 64,544,543	UniSTS	GRCh37
Build 36	11	64,300,856 - 64,301,119	RGD	NCBI36
Celera	11	61,870,779 - 61,871,042	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,871,303 - 60,871,566	UniSTS

REN56416

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,520 - 64,544,769	UniSTS	GRCh37
Build 36	11	64,301,096 - 64,301,345	RGD	NCBI36
Celera	11	61,871,019 - 61,871,268	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,871,543 - 60,871,792	UniSTS

REN56417

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,760 - 64,545,005	UniSTS	GRCh37
Build 36	11	64,301,336 - 64,301,581	RGD	NCBI36
Celera	11	61,871,259 - 61,871,504	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,871,783 - 60,872,028	UniSTS

REN56418

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,544,983 - 64,545,212	UniSTS	GRCh37
Build 36	11	64,301,559 - 64,301,788	RGD	NCBI36
Celera	11	61,871,482 - 61,871,711	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,872,006 - 60,872,235	UniSTS

REN56419

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,545,886 - 64,546,135	UniSTS	GRCh37
Build 36	11	64,302,462 - 64,302,711	RGD	NCBI36
Celera	11	61,872,385 - 61,872,634	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,872,909 - 60,873,158	UniSTS

REN56420

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,124 - 64,546,352	UniSTS	GRCh37
Build 36	11	64,302,700 - 64,302,928	RGD	NCBI36
Celera	11	61,872,623 - 61,872,851	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,873,147 - 60,873,375	UniSTS

REN56421

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,347 - 64,546,609	UniSTS	GRCh37
Build 36	11	64,302,923 - 64,303,185	RGD	NCBI36
Celera	11	61,872,846 - 61,873,108	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,873,370 - 60,873,632	UniSTS

REN56422

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,588 - 64,546,839	UniSTS	GRCh37
Build 36	11	64,303,164 - 64,303,415	RGD	NCBI36
Celera	11	61,873,087 - 61,873,339	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,873,611 - 60,873,865	UniSTS

REN56423

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,664 - 64,546,885	UniSTS	GRCh37
Build 36	11	64,303,240 - 64,303,461	RGD	NCBI36
Celera	11	61,873,163 - 61,873,385	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,873,687 - 60,873,911	UniSTS

REN56424

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,547,088 - 64,547,318	UniSTS	GRCh37
Build 36	11	64,303,664 - 64,303,894	RGD	NCBI36
Celera	11	61,873,588 - 61,873,818	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,874,114 - 60,874,344	UniSTS

REN56425

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,547,274 - 64,547,530	UniSTS	GRCh37
Build 36	11	64,303,850 - 64,304,106	RGD	NCBI36
Celera	11	61,873,774 - 61,874,030	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,874,300 - 60,874,556	UniSTS

REN56426

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,547,614 - 64,547,848	UniSTS	GRCh37
Build 36	11	64,304,190 - 64,304,424	RGD	NCBI36
Celera	11	61,874,114 - 61,874,348	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,874,640 - 60,874,874	UniSTS

REN56427

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,547,834 - 64,548,098	UniSTS	GRCh37
Build 36	11	64,304,410 - 64,304,674	RGD	NCBI36
Celera	11	61,874,334 - 61,874,598	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,874,860 - 60,875,124	UniSTS

REN56428

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,548,046 - 64,548,294	UniSTS	GRCh37
Build 36	11	64,304,622 - 64,304,870	RGD	NCBI36
Celera	11	61,874,546 - 61,874,794	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,875,072 - 60,875,320	UniSTS

ZNF162

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,184 - 64,535,698	UniSTS	GRCh37
Build 36	11	64,291,760 - 64,292,274	RGD	NCBI36
Celera	11	61,861,682 - 61,862,196	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,206 - 60,862,720	UniSTS
GeneMap99-GB4 RH Map	11	240.19	UniSTS
NCBI RH Map	11	573.2	UniSTS

D11S4328

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,537 - 64,543,663	UniSTS	GRCh37
Build 36	11	64,300,113 - 64,300,239	RGD	NCBI36
Celera	11	61,870,036 - 61,870,162	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,870,560 - 60,870,686	UniSTS
GeneMap99-G3 RH Map	11	2809.0	UniSTS

G33087

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,897 - 64,536,015	UniSTS	GRCh37
Build 36	11	64,292,473 - 64,292,591	RGD	NCBI36
Celera	11	61,862,395 - 61,862,513	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	60,862,919 - 60,863,037	UniSTS

stSG635670

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,533,945 - 64,534,968	UniSTS	GRCh37
Build 36	11	64,290,521 - 64,291,544	RGD	NCBI36
Celera	11	61,860,443 - 61,861,466	RGD
HuRef	11	60,860,967 - 60,861,990	UniSTS

stSG635671

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,534,974 - 64,536,004	UniSTS	GRCh37
Build 36	11	64,291,550 - 64,292,580	RGD	NCBI36
Celera	11	61,861,472 - 61,862,502	RGD
HuRef	11	60,861,996 - 60,863,026	UniSTS

stSG635672

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,535,986 - 64,537,469	UniSTS	GRCh37
Build 36	11	64,292,562 - 64,294,045	RGD	NCBI36
Celera	11	61,862,484 - 61,863,967	RGD
HuRef	11	60,863,008 - 60,864,491	UniSTS

stSG635673

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,537,450 - 64,538,634	UniSTS	GRCh37
Build 36	11	64,294,026 - 64,295,210	RGD	NCBI36
Celera	11	61,863,948 - 61,865,132	RGD
HuRef	11	60,864,472 - 60,865,656	UniSTS

stSG635674

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,538,615 - 64,539,672	UniSTS	GRCh37
Build 36	11	64,295,191 - 64,296,248	RGD	NCBI36
Celera	11	61,865,113 - 61,866,170	RGD
HuRef	11	60,865,637 - 60,866,694	UniSTS

stSG635675

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,539,653 - 64,540,916	UniSTS	GRCh37
Build 36	11	64,296,229 - 64,297,492	RGD	NCBI36
Celera	11	61,866,151 - 61,867,414	RGD
HuRef	11	60,866,675 - 60,867,938	UniSTS

stSG635676

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,540,897 - 64,541,949	UniSTS	GRCh37
Build 36	11	64,297,473 - 64,298,525	RGD	NCBI36
Celera	11	61,867,395 - 61,868,447	RGD
HuRef	11	60,867,919 - 60,868,971	UniSTS

stSG635677

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,541,934 - 64,543,105	UniSTS	GRCh37
Build 36	11	64,298,510 - 64,299,681	RGD	NCBI36
Celera	11	61,868,432 - 61,869,603	RGD
HuRef	11	60,868,956 - 60,870,127	UniSTS

stSG635678

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,543,086 - 64,544,533	UniSTS	GRCh37
Build 36	11	64,299,662 - 64,301,109	RGD	NCBI36
Celera	11	61,869,584 - 61,871,032	RGD
HuRef	11	60,870,108 - 60,871,556	UniSTS

stSG635681

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,546,877 - 64,548,115	UniSTS	GRCh37
Build 36	11	64,303,453 - 64,304,691	RGD	NCBI36
Celera	11	61,873,377 - 61,874,615	RGD
HuRef	11	60,873,903 - 60,875,141	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2432

2979

1723

622

1943

464

4355

2190

3705

415

1448

1608

171

1204

2788

Low

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_021399	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001178030	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001178031	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001346363	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001346364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001346409	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001346410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_004630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_201995	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_201997	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_201998	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545246	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018246	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018249	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018250	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018251	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448679	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448680	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427549	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369864	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369865	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369867	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369868	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AI492561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ000051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ000052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK296237	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK299705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001462	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC000773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC008080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC008724	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC011657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC020217	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC032676	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC034451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC038446	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069273	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BE745705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ230035	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU624935	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX095574	(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
	D26120	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D26121	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D26122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC317188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC341853	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC368015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC370979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HF548100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L49345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L49380	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Y08765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Y08766	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000227503 ⟹ ENSP00000227503

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,747 (-)	Ensembl

RefSeq Acc Id:

ENST00000334944 ⟹ ENSP00000334414

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,786 (-)	Ensembl

RefSeq Acc Id:

ENST00000377387 ⟹ ENSP00000366604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,469 (-)	Ensembl

RefSeq Acc Id:

ENST00000377390 ⟹ ENSP00000366607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,542 (-)	Ensembl

RefSeq Acc Id:

ENST00000377394 ⟹ ENSP00000366611

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,747 (-)	Ensembl

RefSeq Acc Id:

ENST00000413725 ⟹ ENSP00000395927

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,765,604 - 64,767,617 (-)	Ensembl

RefSeq Acc Id:

ENST00000413951 ⟹ ENSP00000388470

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,770,297 - 64,778,507 (-)	Ensembl

RefSeq Acc Id:

ENST00000432725 ⟹ ENSP00000406354

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,770,380 - 64,777,761 (-)	Ensembl

RefSeq Acc Id:

ENST00000433274 ⟹ ENSP00000396793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,765,652 - 64,777,760 (-)	Ensembl

RefSeq Acc Id:

ENST00000443908 ⟹ ENSP00000391198

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,765,290 - 64,767,844 (-)	Ensembl

RefSeq Acc Id:

ENST00000448404 ⟹ ENSP00000407962

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,747 (-)	Ensembl

RefSeq Acc Id:

ENST00000463343

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,776,046 - 64,778,763 (-)	Ensembl

RefSeq Acc Id:

ENST00000472725

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,776,046 - 64,778,037 (-)	Ensembl

RefSeq Acc Id:

ENST00000477596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,766,414 - 64,767,646 (-)	Ensembl

RefSeq Acc Id:

ENST00000482693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,773,023 - 64,778,504 (-)	Ensembl

RefSeq Acc Id:

ENST00000486867 ⟹ ENSP00000419062

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,606 - 64,778,771 (-)	Ensembl

RefSeq Acc Id:

ENST00000486960

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,769,278 - 64,770,639 (-)	Ensembl

RefSeq Acc Id:

ENST00000489544

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,768,171 - 64,769,669 (-)	Ensembl

RefSeq Acc Id:

ENST00000496969

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,769,542 - 64,771,607 (-)	Ensembl

RefSeq Acc Id:

ENST00000626028 ⟹ ENSP00000486693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,770,034 - 64,778,763 (-)	Ensembl

RefSeq Acc Id:

ENST00000633899

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,770,278 - 64,778,542 (-)	Ensembl

RefSeq Acc Id:

ENST00000681407 ⟹ ENSP00000505779

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,611 - 64,778,521 (-)	Ensembl

RefSeq Acc Id:

ENST00000706684 ⟹ ENSP00000516498

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,614 - 64,778,533 (-)	Ensembl

RefSeq Acc Id:

ENST00000706685 ⟹ ENSP00000516499

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,764,809 - 64,778,528 (-)	Ensembl

RefSeq Acc Id:

ENST00000706686 ⟹ ENSP00000516500

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,767,759 - 64,778,542 (-)	Ensembl

RefSeq Acc Id:

NM_001178030 ⟹ NP_001171501

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,429,713 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGGTAAGCTGGGC
CCCCCCGGGCTGCCCCCGCTCCCCGGGCCCAAAGGAGGCTTCGAGCCGGGCCCTCCGCCTGCAC
CCGGGCCTGGGGCGGGGCTGCTGGCTCCCGGGCCGCCGCCGCCCCCGCCCGTGGGCTCGATGGG
GGCCCTGACCGCGGCCTTCCCCTTCGCGGCGCTGCCTCCGCCGCCTCCGCCGCCGCCCCCTCCG
CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGC
AGCCGCCCCCTCCGCCGCCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCC
GCCGCGTAAGGACCAGCAGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGG
AAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAG
TTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGA
CCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCT
TCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCA
AAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAA
GCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGAT
GAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACA
TAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGT
TGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCC
AATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCG
AGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGG
GACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATT
ACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCC
AAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCT
CATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACC
ACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCA
TGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCA
CGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTA
CCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCC
CTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCC
TCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAA
GGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTG
GGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCC
GCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAGATCC
CTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCT
TCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTT
ATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCT
TTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCC
GGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGA
GGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCA
AGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCC
TTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATC
CGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCC
TGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTC
CTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGG
GGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTC
TGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCT
TTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTG
TGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001178031 ⟹ NP_001171502

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,777,761 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,429,007 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,067 (-)	NCBI

Sequence:

show sequence

AGACGCAGTGAGGTGGCCGGGCTGTGCGGCGCAACTGTATAGACTGGGGGCCCACTATTGCTGT
CCAGTCCGCTGGTGTCGGGAACAGGGGTGGCGGGTGTTCAGCGCTGGACGGGGTGCTAGCTGTG
AATGCCAGCAGGGCGTGAAAGCCTCACCTGATGACGTGCAGCGACTCCCTTCTGGTCTTGAGGA
ACCAGAATGGGAACCGTACCAAGGATAGCTCCTCTGCTTCTACAGCAAGGCAGGGTTTTCATCC
GGGAGAGACTTCCCAAGTAAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGA
AGACAGTGATTCCAGGAATGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGC
TTATATAGTGCAACTGCAGATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATC
CCCCCTAACCCTGAGGACAGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGC
TTAACACCCGAGAGTTCCGCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGA
GATGGTTGCACTCAATCCGGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTG
AGTGATAAAGTCATGATTCCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCG
GGCCCAGAGGGAACACCCTGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGG
GAAAGGGTCTGTGAAAGAAGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGAT
GAGCCACTTCATGCCCTGGTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGA
TAAGAAACATCCTGAAGCAGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCA
GCTTCGGGAGTTGGCTCGCTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCC
TGGCAGAGCTCAGAGACCCGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTG
GCCACATTGCTTCAGACTGTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGC
ACGGATGGATAAAGAATATTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCT
GTGGGCTCCACCTCTGGGCCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCG
CCAACAACCCACCTCCACCGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTC
TGGCCCTTCAGAGAGTCGGCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGT
GGCCCCCACAGCTTCCCACACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGC
AGCACAACCCCAATGGACCCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGG
CCCCCACCCTCCTGGGCACCATGGCCCTCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTG
GGCTCTGGGGTCTATCGCCTGCATCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGA
TGCCGCCGCCGCCGCCGCCTCCCAGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCC
ATGGCAACAACAGCAGCAGCAGCCTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGT
ACCCCCTTGCCATGGCAGCAAAATACGACGACTACCACCACGAGCGCTGGCACAGGGTCCATCC
CGCCATGGCAACAGCAGCAGGCGGCTGCCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAA
CCCCACTATGGTGCCCCTGCCCCCCGGGGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCT
CCGCCGCCTCCACCGCCTGGTTCCGCCGGCATGATGTATGCCCCGCCCCCTCCTCCTCCGCCTC
CCATGGACCCTTCTAACTTTGTCACCATGATGGGCATGGGGGTGGCGGGCATGCCGCCCTTCGG
GATGCCTCCAGCTCCCCCACCGCCTCCACCACAGAACTAGACTTGTTTTTTAAGAAAATATATA
TTATATATAGAGAGAATTGGTCTCGTTTAAACACGCCGAACCTCACCATATGGAGCCAGACATT
GGGACGCACGCATGTGATTGTGTGTGCACGCATGTGTGTGTGTGCACGCACTGGGCTGGGCCAA
GCGACTGAGGATTCGCTTGGGAACGGGCAGGTGGTAGTAGGGGCGCCAGCTTGGGCTCTCCTGG
CGCCCCGTAGCATCGAGTGTCTTCTTTGTCTTCTTTCTCTCCTCACCCAACTCCCTTTGCCTCT
CCCCAAACCGGGCCGCCAGGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGA
CTTTCCGCGCCCATTGGTGACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGA
TGGTTCGGCAAAGCAGCCTGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCG
TGAAATTTTTATTAATTTTTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGAC
TCCGTCCAAGGAGATGCTCTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCA
GTTCTCCTTCCCTTACCAAGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCAT
GTCAAGCTGGTTGTGGGTTTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGT
GGGGTTTTTTAATCTCTGCCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCA
TCTCCAGGTTTCGGGATTCCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAG
CTCCCTCGGGCTCGCCTGCCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTC
AGATTCCATTTGGTCCTCTCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATG
TCTGAATGTTTTGCAGTGTGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCC
GCTTCCCTCTCCATGAAGTGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTT
TATCTGCAGAAATTTCTCTGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGAT
GTTCCATTGAATAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001346363 ⟹ NP_001333292

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCA
TCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCC
AGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGC
CTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAA
TACGACGACTACCACCACGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGCAGGCG
GCTGCCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCTGCCCC
CCGGGGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCTGGTTC
CGCCGGCATGATGTATGCCCCGCCCCCTCCTCCTCCGCCTCCCATGGACCCTTCTAACTTTGTC
ACCATGATGGGCATGGGGGTGGCGGGCATGCCGCCCTTCGGGATGCCTCCAGCTCCCCCACCGC
CTCCACCACAGAACTAGACTTGTTTTTTAAGAAAATATATATTATATATAGAGAGAATTGGTCT
CGTTTAAACACGCCGAACCTCACCATATGGAGCCAGACATTGGGACGCACGCATGTGATTGTGT
GTGCACGCATGTGTGTGTGTGCACGCACTGGGCTGGGCCAAGCGACTGAGGATTCGCTTGGGAA
CGGGCAGGTGGTAGTAGGGGCGCCAGCTTGGGCTCTCCTGGCGCCCCGTAGCATCGAGTGTCTT
CTTTGTCTTCTTTCTCTCCTCACCCAACTCCCTTTGCCTCTCCCCAAACCGGGCCGCCAGGATC
CCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCC
TTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGT
TATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTC
TTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCC
CGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAG
AGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTC
AAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACC
CTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCAT
CCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGC
CTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTT
CCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAG
GGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATT
CTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGC
TTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGT
GTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001346364 ⟹ NP_001333293

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCA
TCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCC
AGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGC
CTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAG
ATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGA
CCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTG
AGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTT
TTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCT
CCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAG
GAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTT
TTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCC
ACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCC
CATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCC
AGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTC
CTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTG
TAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTG
ATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTG
GGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGC
AGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001346409 ⟹ NP_001333338

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGGTCCCCTTCC
CCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCAAAA
AGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAAGCC
ACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGATGAG
TACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACATAG
AGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGTTGG
GCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCCAAT
ACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCGAGA
CTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGGGAC
CCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATTACC
AACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCCAAA
GGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCAT
GGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACCACA
CCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCATGT
CTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCACGG
CATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTACCC
AGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTT
GGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCCTCC
TCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAAGGA
AAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTGGGC
AGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCCGCC
ACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAGATCCCTC
CCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCTTCC
AGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTTATT
TTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCTTTT
TCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCCGGT
CTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGAGGG
GAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCAAGG
TGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCCTTG
TCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATCCGT
CCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCCTGG
AGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTCCTG
GAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGGGGT
TTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTCTGT
TGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCTTTT
TTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTGTGG
TTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001346410 ⟹ NP_001333339

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGGTCCCCTTCC
CCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCAAAA
AGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAAGCC
ACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGATGAG
TACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACATAG
AGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGTTGG
GCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCCAAT
ACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCGAGA
CTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGGGAC
CCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATTACC
AACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCCAAA
GGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCAT
GGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACCACA
CCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCATGT
CTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCACGG
CATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTACCC
AGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTT
GGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCCTCC
TCCAATGGGTAAATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCA
AGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGT
GGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTC
CGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAGATC
CCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCC
TTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGT
TATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTC
TTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCC
CGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAG
AGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTC
AAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACC
CTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCAT
CCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGC
CTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTT
CCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAG
GGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATT
CTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGC
TTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGT
GTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001378956 ⟹ NP_001365885

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGGTAAGCTGGGC
CCCCCCGGGCTGCCCCCGCTCCCCGGGCCCAAAGGAGGCTTCGAGCCGGGCCCTCCGCCTGCAC
CCGGGCCTGGGGCGGGGCTGCTGGCTCCCGGGCCGCCGCCGCCCCCGCCCGTGGGCTCGATGGG
GGCCCTGACCGCGGCCTTCCCCTTCGCGGCGCTGCCTCCGCCGCCTCCGCCGCCGCCCCCTCCG
CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGC
AGCCGCCCCCTCCGCCGCCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCC
GCCGCGTAAGGACCAGCAGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGG
AAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAG
TTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGA
CCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCT
TCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCA
AAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAA
GCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGAT
GAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACA
TAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGT
TGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCC
AATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCG
AGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGG
GACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATT
ACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCC
AAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCT
CATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACC
ACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCA
TGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCA
CGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTA
CCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCC
CTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCC
TCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAA
GGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTG
GGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCC
GCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAATACG
ACGACTACCACCACGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGCAGGCGGCTG
CCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCTGCCCCCCGG
GGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCTGGTTCCGCC
GGCATGATGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCC
CATTGGTGACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAA
AGCAGCCTGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTA
TTAATTTTTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGG
AGATGCTCTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCC
CTTACCAAGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGT
TGTGGGTTTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTA
ATCTCTGCCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTT
CGGGATTCCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGC
TCGCCTGCCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTT
GGTCCTCTCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTT
TGCAGTGTGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTC
CATGAAGTGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAA
ATTTCTCTGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAA
TAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_001378957 ⟹ NP_001365886

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGGTAAGCTGGGC
CCCCCCGGGCTGCCCCCGCTCCCCGGGCCCAAAGGAGGCTTCGAGCCGGGCCCTCCGCCTGCAC
CCGGGCCTGGGGCGGGGCTGCTGGCTCCCGGGCCGCCGCCGCCCCCGCCCGTGGGCTCGATGGG
GGCCCTGACCGCGGCCTTCCCCTTCGCGGCGCTGCCTCCGCCGCCTCCGCCGCCGCCCCCTCCG
CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGC
AGCCGCCCCCTCCGCCGCCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCC
GCCGCGTAAGGACCAGCAGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGG
AAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAG
TTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGA
CCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCT
TCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCA
AAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAA
GCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGAT
GAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACA
TAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGT
TGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCC
AATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCG
AGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGG
GACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATT
ACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCC
AAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCT
CATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACC
ACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCA
TGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCA
CGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTA
CCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCC
CTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCC
TCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAA
GGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTG
GGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCC
GCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAATACG
ACGACTACCACCACGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGCAGGCGGCTG
CCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCTGCCCCCCGG
GGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCTGGTTCCGCC
GGCATGATGTATGCCCCGCCCCCTCCTCCTCCGCCTCCCATGGACCCTTCTAACTTTGTCACCA
TGATGGGCATGGGGGTGGCGGGCATGCCGCCCTTCGGGATGCCTCCAGCTCCCCCACCGCCTCC
ACCACAGAACTAGACTTGTTTTTTAAGAAAATATATATTATATATAGAGAGAATTGGTCTCGTT
TAAACACGCCGAACCTCACCATATGGAGCCAGACATTGGGACGCACGCATGTGATTGTGTGTGC
ACGCATGTGTGTGTGTGCACGCACTGGGCTGGGCCAAGCGACTGAGGATTCGCTTGGGAACGGG
CAGGTGGTAGTAGGGGCGCCAGCTTGGGCTCTCCTGGCGCCCCGTAGCATCGAGTGTCTTCTTT
GTCTTCTTTCTCTCCTCACCCAACTCCCTTTGCCTCTCCCCAAACCGGGCCGCCAGGATCCCTC
CCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCTTCC
AGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTTATT
TTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCTTTT
TCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCCGGT
CTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGAGGG
GAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCAAGG
TGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCCTTG
TCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATCCGT
CCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCCTGG
AGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTCCTG
GAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGGGGT
TTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTCTGT
TGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCTTTT
TTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTGTGG
TTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_004630 ⟹ NP_004621

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
Build 36	11	64,288,654 - 64,302,817 (-)	NCBI Archive
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGC
CTGCATCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGC
CTCCCAGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCA
GCAGCCTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAG
CAAAATACGACGACTACCACCACGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGC
AGGCGGCTGCCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCT
GCCCCCCGGGGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCT
GGTTCCGCCGGCATGATGTATGCCCCGCCCCCTCCTCCTCCGCCTCCCATGGACCCTTCTAACT
TTGTCACCATGATGGGCATGGGGGTGGCGGGCATGCCGCCCTTCGGGATGCCTCCAGCTCCCCC
ACCGCCTCCACCACAGAACTAGACTTGTTTTTTAAGAAAATATATATTATATATAGAGAGAATT
GGTCTCGTTTAAACACGCCGAACCTCACCATATGGAGCCAGACATTGGGACGCACGCATGTGAT
TGTGTGTGCACGCATGTGTGTGTGTGCACGCACTGGGCTGGGCCAAGCGACTGAGGATTCGCTT
GGGAACGGGCAGGTGGTAGTAGGGGCGCCAGCTTGGGCTCTCCTGGCGCCCCGTAGCATCGAGT
GTCTTCTTTGTCTTCTTTCTCTCCTCACCCAACTCCCTTTGCCTCTCCCCAAACCGGGCCGCCA
GGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGT
GACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCC
TGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTT
TTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCT
CTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCA
AGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGT
TTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTG
CCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATT
CCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTG
CCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTC
TCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTG
TGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAG
TGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTC
TGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGA
GCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_201995 ⟹ NP_973724

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
Build 36	11	64,288,654 - 64,302,817 (-)	NCBI Archive
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGC
CTGCATCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGC
CTCCCAGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCA
GCAGCCTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAG
CAAAATACGACGACTACCACCACGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGC
AGGCGGCTGCCGCAGCTTCTCCAGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCT
GCCCCCCGGGGTCCAGCCGCCTCTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCT
GGTTCCGCCGGCATGATGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACT
TTCCGCGCCCATTGGTGACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATG
GTTCGGCAAAGCAGCCTGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTG
AAATTTTTATTAATTTTTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTC
CGTCCAAGGAGATGCTCTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGT
TCTCCTTCCCTTACCAAGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGT
CAAGCTGGTTGTGGGTTTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGG
GGTTTTTTAATCTCTGCCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATC
TCCAGGTTTCGGGATTCCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCT
CCCTCGGGCTCGCCTGCCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAG
ATTCCATTTGGTCCTCTCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTC
TGAATGTTTTGCAGTGTGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGC
TTCCCTCTCCATGAAGTGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTA
TCTGCAGAAATTTCTCTGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGT
TCCATTGAATAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_201997 ⟹ NP_973726

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
Build 36	11	64,300,082 - 64,302,817 (-)	NCBI Archive
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGGTAAATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTA
TCGCCTGCATCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCG
CCGCCTCCCAGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGC
AGCAGCAGCCTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATG
GCAGCAAAGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCC
CATTGGTGACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAA
AGCAGCCTGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTA
TTAATTTTTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGG
AGATGCTCTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCC
CTTACCAAGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGT
TGTGGGTTTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTA
ATCTCTGCCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTT
CGGGATTCCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGC
TCGCCTGCCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTT
GGTCCTCTCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTT
TGCAGTGTGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTC
CATGAAGTGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAA
ATTTCTCTGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAA
TAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

NM_201998 ⟹ NP_973727

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI
GRCh37	11	64,532,076 - 64,546,515 (-)	NCBI
Build 36	11	64,288,654 - 64,302,817 (-)	NCBI Archive
HuRef	11	60,858,921 - 60,873,339 (-)	ENTREZGENE
CHM1_1	11	64,415,846 - 64,430,091 (-)	NCBI
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Sequence:

show sequence

GTGCGTCTCGCGCCGCCGCCGCCCGCCGCGTGAGAGGACGGGCTCCGCGCGCTCCGGCAGCGCA
TTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCC
GGTGCCTGTCCCCGGGGGCGCCATGGCGACCGGAGCGAACGCCACGCCGTTGGACTTCCCAAGT
AAGAAGCGGAAGAGGAGCCGCTGGAACCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAA
TGCCTACAGTTATTCCCCCTGGACTTACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCA
GATAGAAGACCTGACTCGTAAACTGCGCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGAC
AGGTCCCCTTCCCCTGAGCCCATCTACAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCC
GCACCCGCAAAAAGCTGGAAGAGGAGCGGCACAACCTCATCACAGAGATGGTTGCACTCAATCC
GGATTTCAAGCCACCTGCAGATTACAAACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATT
CCACAAGATGAGTACCCAGAAATCAACTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCC
TGAAGAACATAGAGAAGGAGTGCAATGCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGA
AGGGAAGGTTGGGCGCAAAGATGGCCAGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTG
GTTACTGCCAATACAATGGAGAACGTCAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGC
AGGGTATCGAGACTCCAGAGGACCAGAATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCG
CTTAAATGGGACCCTTCGGGAAGACGATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACC
CGCAGCATTACCAACACCACAGTGTGTACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACT
GTAAATTCCAAAGGCCTGGTGATCCTCAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATA
TTTGTCCCTCATGGCTGAACTGGGTGAAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGG
CCTGCCACCACACCCCTGGCCAGCGCACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCAC
CGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG
GCCCTACCACGGCATGCATGGAGGTGGTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCA
CACCCATTACCCAGCCTGACAGGTGGGCATGGTGGACATCCCATGCAGCACAACCCCAATGGAC
CCCCACCCCCTTGGATGCAGCCACCACCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCA
CCATGGCCCTCCTCCAATGGATCAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGC
CTGCATCAAGGAAAAGGTATGATGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGC
CTCCCAGTGGGCAGCCCCCACCCCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCA
GCAGCCTCCGCCACCCCCTCCGCCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAG
CAAAGATCCCTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATT
GGTGACCCTTCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCA
GCCTGAGTTATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAA
TTTTTTTCTTTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGAT
GCTCTCCCCGGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTA
CCAAGGAGAGGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTG
GGTTTTTCAAGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCT
CTGCCACCCTTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGG
ATTCCCATCCGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGC
CTGCCAGCCTGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTC
CTCTCCTTCCTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCA
GTGTGTAGGGGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATG
AAGTGATTCTGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTT
CTCTGGGCTTTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAA
AGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

XM_011545247 ⟹ XP_011543549

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

Sequence:

show sequence

GCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCAGCCGCCCCCTCCGCCG
CCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCCGCCGCGTAAGGACCAGC
AGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGGAAGAGGAGCCGCTGGAA
CCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAGTTATTCCCCCTGGACTT
ACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGACCTGACTCGTAAACTGC
GCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCTTCCCCTGAGCCCATCTA
CAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCAAAAAGCTGGAAGAGGAG
CGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAAGCCACCTGCAGATTACA
AACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGATGAGTACCCAGAAATCAA
CTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACATAGAGAAGGAGTGCAAT
GCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGTTGGGCGCAAAGATGGCC
AGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCCAATACAATGGAGAACGT
CAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCGAGACTCCAGAGGACCAG
AATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGGGACCCTTCGGGAAGACG
ATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATTACCAACACCACAGTGTG
TACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCCAAAGGCCTGGTGATCCT
CAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCATGGCTGAACTGGGTG
AAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACCACACCCCTGGCCAGCGC
ACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCATGTCTACCACCCAGAGC
CGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCACGGCATGCATGGAGGTG
GTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTACCCAGCCTGACAGGTGG
GCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTTGGATGCAGCCACCA
CCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCCTCCTCCAATGGGTAAAT
CAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAAGGAAAAGGTATGA
TGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTGGGCAGCCCCCACC
CCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCCGCCACCCCCTCCG
CCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAATACGACGACTACCACCA
CGAGCGCTGGCACAGGGTCCATCCCGCCATGGCAACAGCAGCAGGCGGCTGCCGCAGCTTCTCC
AGGAGCCCCTCAGATGCAAGGCAACCCCACTATGGTGCCCCTGCCCCCCGGGGTCCAGCCGCCT
CTGCCGCCTGGGGCCCCTCCCCCTCCGCCGCCTCCACCGCCTGGTTCCGCCGGCATGATGATCC
CTCCCCGCGGCGGCGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCT
TCCAGGCAGACAGCCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTT
ATTTTTGTGGACGGAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCT
TTTTCCTTTGTTACTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCC
GGTCTTCTGCTGCAATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGA
GGGGAGCAAATGGTTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCA
AGGTGCCATAGCCACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCC
TTGTCAAGGGAGTCTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATC
CGTCCTGGCGATCCTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCC
TGGAGTTCTTCCTGTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTC
CTGGAAGGCTTCCTTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGG
GGTTTGAGCCCCTTGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTC
TGTTGACAATAATGTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCT
TTTTTCGGTGTTAGATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTG
TGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

XM_011545248 ⟹ XP_011543550

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

Sequence:

show sequence

GCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCAGCCGCCCCCTCCGCCG
CCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCCGCCGCGTAAGGACCAGC
AGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGGAAGAGGAGCCGCTGGAA
CCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAGTTATTCCCCCTGGACTT
ACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGACCTGACTCGTAAACTGC
GCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCTTCCCCTGAGCCCATCTA
CAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCAAAAAGCTGGAAGAGGAG
CGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAAGCCACCTGCAGATTACA
AACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGATGAGTACCCAGAAATCAA
CTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACATAGAGAAGGAGTGCAAT
GCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGTTGGGCGCAAAGATGGCC
AGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCCAATACAATGGAGAACGT
CAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCGAGACTCCAGAGGACCAG
AATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGGGACCCTTCGGGAAGACG
ATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATTACCAACACCACAGTGTG
TACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCCAAAGGCCTGGTGATCCT
CAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCATGGCTGAACTGGGTG
AAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACCACACCCCTGGCCAGCGC
ACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCATGTCTACCACCCAGAGC
CGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCACGGCATGCATGGAGGTG
GTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTACCCAGCCTGACAGGTGG
GCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTTGGATGCAGCCACCA
CCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCCTCCTCCAATGGGTAAAT
CAGTACCTGGGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAAGGAAAAGGTATGA
TGCCGCCACCACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTGGGCAGCCCCCACC
CCCTCCCTCTGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCCGCCACCCCCTCCG
CCCAGCAGCAGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAGATCCCTCCCCGCGGCGG
CGATGGCCCGAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCTTCCAGGCAGACAG
CCTCAGCAACGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTTATTTTTGTGGACG
GAATCGGAACACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCTTTTTCCTTTGTTA
CTTCTTTATCTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCCGGTCTTCTGCTGC
AATTTAGATTCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGAGGGGAGCAAATGG
TTTTGGGCAAGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCAAGGTGCCATAGCC
ACCCCCAAAGATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCCTTGTCAAGGGAGT
CTTGTAAAGTTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATCCGTCCTGGCGATC
CTGCCAGCAGTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCCTGGAGTTCTTCCT
GTGCTCCTTGATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTCCTGGAAGGCTTCC
TTTTATGTTTTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGGGGTTTGAGCCCCT
TGTTCATTCTCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTCTGTTGACAATAAT
GTATACTGCGCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCTTTTTTCGGTGTTA
GATTCAACACTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

XM_017018246 ⟹ XP_016873735

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

Sequence:

show sequence

GCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCAGCCGCCCCCTCCGCCG
CCGCTCTACCAGCGCGTGTCGCCGCCGCAGCCGCCGCCACCCCAGCCGCCGCGTAAGGACCAGC
AGCCGGGCCCGGCCGGCGGCGGAGGAGACTTCCCAAGTAAGAAGCGGAAGAGGAGCCGCTGGAA
CCAAGACACAATGGAACAGAAGACAGTGATTCCAGGAATGCCTACAGTTATTCCCCCTGGACTT
ACTCGAGAACAAGAAAGAGCTTATATAGTGCAACTGCAGATAGAAGACCTGACTCGTAAACTGC
GCACAGGAGACCTGGGCATCCCCCCTAACCCTGAGGACAGGTCCCCTTCCCCTGAGCCCATCTA
CAATAGCGAGGGGAAGCGGCTTAACACCCGAGAGTTCCGCACCCGCAAAAAGCTGGAAGAGGAG
CGGCACAACCTCATCACAGAGATGGTTGCACTCAATCCGGATTTCAAGCCACCTGCAGATTACA
AACCTCCAGCAACACGTGTGAGTGATAAAGTCATGATTCCACAAGATGAGTACCCAGAAATCAA
CTTTGTGGGGCTGCTCATCGGGCCCAGAGGGAACACCCTGAAGAACATAGAGAAGGAGTGCAAT
GCCAAGATTATGATCCGGGGGAAAGGGTCTGTGAAAGAAGGGAAGGTTGGGCGCAAAGATGGCC
AGATGTTGCCAGGAGAAGATGAGCCACTTCATGCCCTGGTTACTGCCAATACAATGGAGAACGT
CAAAAAGGCAGTGGAACAGATAAGAAACATCCTGAAGCAGGGTATCGAGACTCCAGAGGACCAG
AATGATCTACGGAAGATGCAGCTTCGGGAGTTGGCTCGCTTAAATGGGACCCTTCGGGAAGACG
ATAACAGGATCTTAAGACCCTGGCAGAGCTCAGAGACCCGCAGCATTACCAACACCACAGTGTG
TACCAAGTGTGGAGGGGCTGGCCACATTGCTTCAGACTGTAAATTCCAAAGGCCTGGTGATCCT
CAGTCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCATGGCTGAACTGGGTG
AAGCACCTGTCCCAGCATCTGTGGGCTCCACCTCTGGGCCTGCCACCACACCCCTGGCCAGCGC
ACCTCGTCCTGCTGCTCCCGCCAACAACCCACCTCCACCGTCTCTCATGTCTACCACCCAGAGC
CGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCGGCCCTACCACGGCATGCATGGAGGTG
GTCCTGGTGGGCCCGGAGGTGGCCCCCACAGCTTCCCACACCCATTACCCAGCCTGACAGGTGG
GCATGGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTTGGATGCAGCCACCA
CCACCACCGATGAACCAGGGCCCCCACCCTCCTGGGCACCATGGCCCTCCTCCAATGGTACCTG
GGAAGTACGCCTGTGGGCTCTGGGGTCTATCGCCTGCATCAAGGAAAAGGTATGATGCCGCCAC
CACCTATGGGCATGATGCCGCCGCCGCCGCCGCCTCCCAGTGGGCAGCCCCCACCCCCTCCCTC
TGGTCCTCTTCCCCCATGGCAACAACAGCAGCAGCAGCCTCCGCCACCCCCTCCGCCCAGCAGC
AGTATGGCTTCCAGTACCCCCTTGCCATGGCAGCAAAGATCCCTCCCCGCGGCGGCGATGGCCC
GAGCCATGAGAGTGAGGACTTTCCGCGCCCATTGGTGACCCTTCCAGGCAGACAGCCTCAGCAA
CGCCCCTGGTGGACAGGATGGTTCGGCAAAGCAGCCTGAGTTATTTTTGTGGACGGAATCGGAA
CACGCTGGCTCCATATCGTGAAATTTTTATTAATTTTTTTCTTTTTCCTTTGTTACTTCTTTAT
CTTTTCCTTTCTTCAGACTCCGTCCAAGGAGATGCTCTCCCCGGTCTTCTGCTGCAATTTAGAT
TCCTTTCCCTTCTCTCCAGTTCTCCTTCCCTTACCAAGGAGAGGGGAGCAAATGGTTTTGGGCA
AGGGCTTTGGCCATTCATGTCAAGCTGGTTGTGGGTTTTTCAAGGTGCCATAGCCACCCCCAAA
GATGTTTGTTTAAAGCGTGGGGTTTTTTAATCTCTGCCACCCTTGTCAAGGGAGTCTTGTAAAG
TTGCCGAGGGTAGGTTCATCTCCAGGTTTCGGGATTCCCATCCGTCCTGGCGATCCTGCCAGCA
GTGGGTGGGCAGCCTGAGCTCCCTCGGGCTCGCCTGCCAGCCTGGAGTTCTTCCTGTGCTCCTT
GATCACCTGAGCTGCCTCAGATTCCATTTGGTCCTCTCCTTCCTGGAAGGCTTCCTTTTATGTT
TTGTTTTAATCCCAAATGTCTGAATGTTTTGCAGTGTGTAGGGGTTTGAGCCCCTTGTTCATTC
TCCTTCCTTTTTCCTCCCGCTTCCCTCTCCATGAAGTGATTCTGTTGACAATAATGTATACTGC
GCGTTCTCTTCACTGGTTTATCTGCAGAAATTTCTCTGGGCTTTTTTCGGTGTTAGATTCAACA
CTGCGCTAAAGCGGGGATGTTCCATTGAATAAAAGAGCAGTGTGGTTTTCTGGG

hide sequence

RefSeq Acc Id:

XM_047427549 ⟹ XP_047283505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

RefSeq Acc Id:

XM_047427550 ⟹ XP_047283506

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

RefSeq Acc Id:

XM_047427551 ⟹ XP_047283507

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,764,606 - 64,778,542 (-)	NCBI

RefSeq Acc Id:

XM_054369864 ⟹ XP_054225839

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

RefSeq Acc Id:

XM_054369865 ⟹ XP_054225840

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

RefSeq Acc Id:

XM_054369866 ⟹ XP_054225841

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

RefSeq Acc Id:

XM_054369867 ⟹ XP_054225842

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

RefSeq Acc Id:

XM_054369868 ⟹ XP_054225843

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

RefSeq Acc Id:

XM_054369869 ⟹ XP_054225844

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,757,911 - 64,771,848 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001171501	(Get FASTA)	NCBI Sequence Viewer
	NP_001171502	(Get FASTA)	NCBI Sequence Viewer
	NP_001333292	(Get FASTA)	NCBI Sequence Viewer
	NP_001333293	(Get FASTA)	NCBI Sequence Viewer
	NP_001333338	(Get FASTA)	NCBI Sequence Viewer
	NP_001333339	(Get FASTA)	NCBI Sequence Viewer
	NP_001365885	(Get FASTA)	NCBI Sequence Viewer
	NP_001365886	(Get FASTA)	NCBI Sequence Viewer
	NP_004621	(Get FASTA)	NCBI Sequence Viewer
	NP_973724	(Get FASTA)	NCBI Sequence Viewer
	NP_973726	(Get FASTA)	NCBI Sequence Viewer
	NP_973727	(Get FASTA)	NCBI Sequence Viewer
	XP_011543549	(Get FASTA)	NCBI Sequence Viewer
	XP_011543550	(Get FASTA)	NCBI Sequence Viewer
	XP_016873735	(Get FASTA)	NCBI Sequence Viewer
	XP_047283505	(Get FASTA)	NCBI Sequence Viewer
	XP_047283506	(Get FASTA)	NCBI Sequence Viewer
	XP_047283507	(Get FASTA)	NCBI Sequence Viewer
	XP_054225839	(Get FASTA)	NCBI Sequence Viewer
	XP_054225840	(Get FASTA)	NCBI Sequence Viewer
	XP_054225841	(Get FASTA)	NCBI Sequence Viewer
	XP_054225842	(Get FASTA)	NCBI Sequence Viewer
	XP_054225843	(Get FASTA)	NCBI Sequence Viewer
	XP_054225844	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB03514	(Get FASTA)	NCBI Sequence Viewer
	AAB04033	(Get FASTA)	NCBI Sequence Viewer
	AAH00773	(Get FASTA)	NCBI Sequence Viewer
	AAH08080	(Get FASTA)	NCBI Sequence Viewer
	AAH08724	(Get FASTA)	NCBI Sequence Viewer
	AAH20217	(Get FASTA)	NCBI Sequence Viewer
	AAH38446	(Get FASTA)	NCBI Sequence Viewer
	BAA05116	(Get FASTA)	NCBI Sequence Viewer
	BAA05117	(Get FASTA)	NCBI Sequence Viewer
	BAA05118	(Get FASTA)	NCBI Sequence Viewer
	BAA05119	(Get FASTA)	NCBI Sequence Viewer
	BAG58956	(Get FASTA)	NCBI Sequence Viewer
	BAG61606	(Get FASTA)	NCBI Sequence Viewer
	BAG63254	(Get FASTA)	NCBI Sequence Viewer
	BAH11587	(Get FASTA)	NCBI Sequence Viewer
	CAA03883	(Get FASTA)	NCBI Sequence Viewer
	CAA70018	(Get FASTA)	NCBI Sequence Viewer
	CAA70019	(Get FASTA)	NCBI Sequence Viewer
	CCO13811	(Get FASTA)	NCBI Sequence Viewer
	EAW74286	(Get FASTA)	NCBI Sequence Viewer
	EAW74287	(Get FASTA)	NCBI Sequence Viewer
	EAW74288	(Get FASTA)	NCBI Sequence Viewer
	EAW74289	(Get FASTA)	NCBI Sequence Viewer
	EAW74290	(Get FASTA)	NCBI Sequence Viewer
	EAW74291	(Get FASTA)	NCBI Sequence Viewer
	EAW74292	(Get FASTA)	NCBI Sequence Viewer
	EAW74293	(Get FASTA)	NCBI Sequence Viewer
	EAW74294	(Get FASTA)	NCBI Sequence Viewer
	EAW74295	(Get FASTA)	NCBI Sequence Viewer
	EAW74296	(Get FASTA)	NCBI Sequence Viewer
	EAW74297	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000227503
	ENSP00000227503.9
	ENSP00000334414
	ENSP00000334414.5
	ENSP00000366604
	ENSP00000366604.1
	ENSP00000366607
	ENSP00000366607.3
	ENSP00000366611
	ENSP00000366611.3
	ENSP00000388470.1
	ENSP00000391198.1
	ENSP00000395927.1
	ENSP00000396793
	ENSP00000396793.2
	ENSP00000406354.1
	ENSP00000407962.1
	ENSP00000419062
	ENSP00000419062.2
	ENSP00000505779
	ENSP00000505779.1
	ENSP00000516498
	ENSP00000516498.1
	ENSP00000516499.1
	ENSP00000516500.1
GenBank Protein	Q15637	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_973727 ⟸ NM_201998
- Peptide Label:	isoform 3
- UniProtKB:	B4DSE4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMD QYLGSTPVGSGVYRLHQGKGMMPPPPMGMMPPPPPPPSGQPPPPPSGPLPPWQQQQQQPPPPPP PSSSMASSTPLPWQQRSLPAAAMARAMRVRTFRAHW hide sequence

RefSeq Acc Id:	NP_973724 ⟸ NM_201995
- Peptide Label:	isoform 2
- UniProtKB:	B4DJU4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMD QYLGSTPVGSGVYRLHQGKGMMPPPPMGMMPPPPPPPSGQPPPPPSGPLPPWQQQQQQPPPPPP PSSSMASSTPLPWQQNTTTTTTSAGTGSIPPWQQQQAAAAASPGAPQMQGNPTMVPLPPGVQPP LPPGAPPPPPPPPPGSAGMMIPPRGGDGPSHESEDFPRPLVTLPGRQPQQRPWWTGWFGKAA hide sequence

RefSeq Acc Id:	NP_004621 ⟸ NM_004630
- Peptide Label:	isoform 1
- UniProtKB:	Q9BW01 (UniProtKB/Swiss-Prot), Q969H7 (UniProtKB/Swiss-Prot), Q92745 (UniProtKB/Swiss-Prot), Q92744 (UniProtKB/Swiss-Prot), Q8IY00 (UniProtKB/Swiss-Prot), Q15913 (UniProtKB/Swiss-Prot), Q14819 (UniProtKB/Swiss-Prot), Q14818 (UniProtKB/Swiss-Prot), C9JJE2 (UniProtKB/Swiss-Prot), B7Z1Q1 (UniProtKB/Swiss-Prot), Q9UEI0 (UniProtKB/Swiss-Prot), Q15637 (UniProtKB/Swiss-Prot), B4DJU4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMD QYLGSTPVGSGVYRLHQGKGMMPPPPMGMMPPPPPPPSGQPPPPPSGPLPPWQQQQQQPPPPPP PSSSMASSTPLPWQQNTTTTTTSAGTGSIPPWQQQQAAAAASPGAPQMQGNPTMVPLPPGVQPP LPPGAPPPPPPPPPGSAGMMYAPPPPPPPPMDPSNFVTMMGMGVAGMPPFGMPPAPPPPPPQN hide sequence

RefSeq Acc Id:	NP_973726 ⟸ NM_201997
- Peptide Label:	isoform 4
- UniProtKB:	A0A9L9PXR5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMG KSVPGKYACGLWGLSPASRKRYDAATTYGHDAAAAAASQWAAPTPSLWSSSPMATTAAAASATP SAQQQYGFQYPLAMAAKIPPRGGDGPSHESEDFPRPLVTLPGRQPQQRPWWTGWFGKAA hide sequence

RefSeq Acc Id:	NP_001171501 ⟸ NM_001178030
- Peptide Label:	isoform 6
- UniProtKB:	Q15637 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MATGANATPLGKLGPPGLPPLPGPKGGFEPGPPPAPGPGAGLLAPGPPPPPPVGSMGALTAAFP FAALPPPPPPPPPPPPQQPPPPPPPPSPGASYPPPQPPPPPPLYQRVSPPQPPPPQPPRKDQQP GPAGGGGDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRKLRT GDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPADYKP PATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKDGQM LPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLREDDN RILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAELGEA PVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHGGGP GGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMDQYL GSTPVGSGVYRLHQGKGMMPPPPMGMMPPPPPPPSGQPPPPPSGPLPPWQQQQQQPPPPPPPSS SMASSTPLPWQQRSLPAAAMARAMRVRTFRAHW hide sequence

RefSeq Acc Id:	NP_001171502 ⟸ NM_001178031
- Peptide Label:	isoform 5
- UniProtKB:	B4DJU4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRKLRTGDLGIPPNPEDRSPSPEPIYNSE GKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVG LLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKA VEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKC GGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRP AAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGG HPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMDQYLGSTPVGSGVYRLHQGKGMMPPPP MGMMPPPPPPPSGQPPPPPSGPLPPWQQQQQQPPPPPPPSSSMASSTPLPWQQNTTTTTTSAGT GSIPPWQQQQAAAAASPGAPQMQGNPTMVPLPPGVQPPLPPGAPPPPPPPPPGSAGMMYAPPPP PPPPMDPSNFVTMMGMGVAGMPPFGMPPAPPPPPPQN hide sequence

RefSeq Acc Id:

XP_011543550 ⟸ XM_011545248

- Peptide Label:

isoform X4

- Sequence:

show sequence

MEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRKLRTGDLGIPPNPEDRSPSPEPIYNSE
GKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVG
LLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKA
VEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKC
GGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRP
AAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGG
HPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMGKSVPGKYACGLWGLSPASRKRYDAAT
TYGHDAAAAAASQWAAPTPSLWSSSPMATTAAAASATPSAQQQYGFQYPLAMAAKIPPRGGDGP
SHESEDFPRPLVTLPGRQPQQRPWWTGWFGKAA

hide sequence

RefSeq Acc Id:

XP_011543549 ⟸ XM_011545247

- Peptide Label:

isoform X3

- Sequence:

show sequence

MEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRKLRTGDLGIPPNPEDRSPSPEPIYNSE
GKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVG
LLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKA
VEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKC
GGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRP
AAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGG
HPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMGKSVPGKYACGLWGLSPASRKRYDAAT
TYGHDAAAAAASQWAAPTPSLWSSSPMATTAAAASATPSAQQQYGFQYPLAMAAKYDDYHHERW
HRVHPAMATAAGGCRSFSRSPSDARQPHYGAPAPRGPAASAAWGPSPSAASTAWFRRHDDPSPR
RRWPEP

hide sequence

RefSeq Acc Id:

XP_016873735 ⟸ XM_017018246

- Peptide Label:

isoform X2

- Sequence:

show sequence

MEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRKLRTGDLGIPPNPEDRSPSPEPIYNSE
GKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVG
LLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKA
VEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKC
GGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRP
AAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGG
HPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMVPGKYACGLWGLSPASRKRYDAATTYG
HDAAAAAASQWAAPTPSLWSSSPMATTAAAASATPSAQQQYGFQYPLAMAAKIPPRGGDGPSHE
SEDFPRPLVTLPGRQPQQRPWWTGWFGKAA

hide sequence

RefSeq Acc Id:	NP_001333338 ⟸ NM_001346409
- Peptide Label:	isoform 7
- UniProtKB:	B4DX42 (UniProtKB/TrEMBL), E7ESU3 (UniProtKB/TrEMBL), B4DSE4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRG KGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQ LRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKA RMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNS GPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQG PHPPGHHGPPPMDQYLGSTPVGSGVYRLHQGKGMMPPPPMGMMPPPPPPPSGQPPPPPSGPLPP WQQQQQQPPPPPPPSSSMASSTPLPWQQRSLPAAAMARAMRVRTFRAHW hide sequence

RefSeq Acc Id:

NP_001333339 ⟸ NM_001346410

- Peptide Label:

isoform 8

- Sequence:

show sequence

MVALNPDFKPPADYKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRG
KGSVKEGKVGRKDGQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQ
LRELARLNGTLREDDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKA
RMDKEYLSLMAELGEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNS
GPSESRPYHGMHGGGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQG
PHPPGHHGPPPMGKSVPGKYACGLWGLSPASRKRYDAATTYGHDAAAAAASQWAAPTPSLWSSS
PMATTAAAASATPSAQQQYGFQYPLAMAAKIPPRGGDGPSHESEDFPRPLVTLPGRQPQQRPWW
TGWFGKAA

hide sequence

RefSeq Acc Id:	NP_001333293 ⟸ NM_001346364
- Peptide Label:	isoform 10
- UniProtKB:	A0A9L9PXR5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMV PGKYACGLWGLSPASRKRYDAATTYGHDAAAAAASQWAAPTPSLWSSSPMATTAAAASATPSAQ QQYGFQYPLAMAAKIPPRGGDGPSHESEDFPRPLVTLPGRQPQQRPWWTGWFGKAA hide sequence

RefSeq Acc Id:	NP_001333292 ⟸ NM_001346363
- Peptide Label:	isoform 9
- UniProtKB:	A0A9L9PXR5 (UniProtKB/TrEMBL), H7C561 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATGANATPLDFPSKKRKRSRWNQDTMEQKTVIPGMPTVIPPGLTREQERAYIVQLQIEDLTRK LRTGDLGIPPNPEDRSPSPEPIYNSEGKRLNTREFRTRKKLEEERHNLITEMVALNPDFKPPAD YKPPATRVSDKVMIPQDEYPEINFVGLLIGPRGNTLKNIEKECNAKIMIRGKGSVKEGKVGRKD GQMLPGEDEPLHALVTANTMENVKKAVEQIRNILKQGIETPEDQNDLRKMQLRELARLNGTLRE DDNRILRPWQSSETRSITNTTVCTKCGGAGHIASDCKFQRPGDPQSAQDKARMDKEYLSLMAEL GEAPVPASVGSTSGPATTPLASAPRPAAPANNPPPPSLMSTTQSRPPWMNSGPSESRPYHGMHG GGPGGPGGGPHSFPHPLPSLTGGHGGHPMQHNPNGPPPPWMQPPPPPMNQGPHPPGHHGPPPMV PGKYACGLWGLSPASRKRYDAATTYGHDAAAAAASQWAAPTPSLWSSSPMATTAAAASATPSAQ QQYGFQYPLAMAAKYDDYHHERWHRVHPAMATAAGGCRSFSRSPSDARQPHYGAPAPRGPAASA AWGPSPSAASTAWFRRHDVCPAPSSSASHGPF hide sequence

RefSeq Acc Id:	NP_001365885 ⟸ NM_001378956
- Peptide Label:	isoform 11
- UniProtKB:	A0A9L9PXE4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	NP_001365886 ⟸ NM_001378957
- Peptide Label:	isoform 12
- UniProtKB:	A0A7P0T9U7 (UniProtKB/TrEMBL), B4DJU4 (UniProtKB/TrEMBL)

RefSeq Acc Id:

ENSP00000227503 ⟸ ENST00000227503

RefSeq Acc Id:

ENSP00000334414 ⟸ ENST00000334944

RefSeq Acc Id:

ENSP00000388470 ⟸ ENST00000413951

RefSeq Acc Id:

ENSP00000395927 ⟸ ENST00000413725

RefSeq Acc Id:

ENSP00000486693 ⟸ ENST00000626028

RefSeq Acc Id:

ENSP00000366611 ⟸ ENST00000377394

RefSeq Acc Id:

ENSP00000366604 ⟸ ENST00000377387

RefSeq Acc Id:

ENSP00000366607 ⟸ ENST00000377390

RefSeq Acc Id:

ENSP00000391198 ⟸ ENST00000443908

RefSeq Acc Id:

ENSP00000406354 ⟸ ENST00000432725

RefSeq Acc Id:

ENSP00000396793 ⟸ ENST00000433274

RefSeq Acc Id:

ENSP00000419062 ⟸ ENST00000486867

RefSeq Acc Id:

ENSP00000407962 ⟸ ENST00000448404

RefSeq Acc Id:

ENSP00000505779 ⟸ ENST00000681407

RefSeq Acc Id:	XP_047283507 ⟸ XM_047427551
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047283506 ⟸ XM_047427550
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047283505 ⟸ XM_047427549
- Peptide Label:	isoform X1

RefSeq Acc Id:

ENSP00000516500 ⟸ ENST00000706686

RefSeq Acc Id:

ENSP00000516498 ⟸ ENST00000706684

RefSeq Acc Id:

ENSP00000516499 ⟸ ENST00000706685

RefSeq Acc Id:	XP_054225844 ⟸ XM_054369869
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054225843 ⟸ XM_054369868
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054225840 ⟸ XM_054369865
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054225839 ⟸ XM_054369864
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054225842 ⟸ XM_054369867
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054225841 ⟸ XM_054369866
- Peptide Label:	isoform X3

Protein Domains

CCHC-type KH Splicing factor 1 helix-hairpin

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q15637-F1-model_v2	AlphaFold	Q15637	1-639	view protein structure

Promoters

RGD ID:

6789354

Promoter ID:

HG_KWN:13258

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000143251, OTTHUMT00000143252, OTTHUMT00000343496

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,291,411 - 64,292,882 (-)	MPROMDB

RGD ID:

6789353

Promoter ID:

HG_KWN:13259

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000315957

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,293,221 - 64,294,282 (-)	MPROMDB

RGD ID:

6789349

Promoter ID:

HG_KWN:13260

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000143246

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,294,311 - 64,295,662 (-)	MPROMDB

RGD ID:

6789351

Promoter ID:

HG_KWN:13261

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000143250

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,295,571 - 64,296,212 (-)	MPROMDB

RGD ID:

6789352

Promoter ID:

HG_KWN:13262

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:

ENST00000377387, NM_001178031, NM_004630, NM_201995, NM_201997, NM_201998, NR_033649, NR_033650, OTTHUMT00000143247, OTTHUMT00000143248, OTTHUMT00000143249, OTTHUMT00000157360, OTTHUMT00000331962, UC001OBF.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	64,301,621 - 64,303,272 (-)	MPROMDB

RGD ID:

7220919

Promoter ID:

EPDNEW_H16204

Type:

initiation region

Name:

SF1_2

Description:

splicing factor 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16205

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,778,531 - 64,778,591	EPDNEW

RGD ID:

7220917

Promoter ID:

EPDNEW_H16205

Type:

initiation region

Name:

SF1_1

Description:

splicing factor 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16204

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,778,769 - 64,778,829	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12950	AgrOrtholog
COSMIC	SF1	COSMIC
Ensembl Genes	ENSG00000168066	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000227503	ENTREZGENE
	ENST00000227503.13	UniProtKB/Swiss-Prot
	ENST00000334944	ENTREZGENE
	ENST00000334944.9	UniProtKB/Swiss-Prot
	ENST00000377387	ENTREZGENE
	ENST00000377387.5	UniProtKB/Swiss-Prot
	ENST00000377390	ENTREZGENE
	ENST00000377390.8	UniProtKB/Swiss-Prot
	ENST00000377394	ENTREZGENE
	ENST00000377394.7	UniProtKB/Swiss-Prot
	ENST00000413725.5	UniProtKB/TrEMBL
	ENST00000413951.5	UniProtKB/TrEMBL
	ENST00000432725.1	UniProtKB/TrEMBL
	ENST00000433274	ENTREZGENE
	ENST00000433274.6	UniProtKB/Swiss-Prot
	ENST00000443908.5	UniProtKB/TrEMBL
	ENST00000448404.5	UniProtKB/TrEMBL
	ENST00000486867	ENTREZGENE
	ENST00000486867.2	UniProtKB/TrEMBL
	ENST00000681407	ENTREZGENE
	ENST00000681407.1	UniProtKB/TrEMBL
	ENST00000706684	ENTREZGENE
	ENST00000706684.1	UniProtKB/TrEMBL
	ENST00000706685.1	UniProtKB/TrEMBL
	ENST00000706686.1	UniProtKB/TrEMBL
Gene3D-CATH	3.30.1370.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	6.10.140.1790	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000168066	GTEx
HGNC ID	HGNC:12950	ENTREZGENE
Human Proteome Map	SF1	Human Proteome Map
InterPro	BBP-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	KH_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	KH_dom_type_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	KH_dom_type_1_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SF1-HH	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SF1-HH_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_CCHC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7536	UniProtKB/Swiss-Prot
NCBI Gene	7536	ENTREZGENE
OMIM	601516	OMIM
PANTHER	PTHR11208	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR11208:SF45	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	KH_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SF1-HH	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-CCHC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37533	PharmGKB
PRINTS	PRICHEXTENSN	UniProtKB/TrEMBL
PROSITE	KH_TYPE_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZF_CCHC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	SM00322	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_C2HC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF54791	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A7P0T9U7	ENTREZGENE, UniProtKB/TrEMBL
	A0A9L9PXE4	ENTREZGENE, UniProtKB/TrEMBL
	A0A9L9PXR5	ENTREZGENE, UniProtKB/TrEMBL
	A0A9L9PXU0_HUMAN	UniProtKB/TrEMBL
	B4DJU4	ENTREZGENE, UniProtKB/TrEMBL
	B4DSE4	ENTREZGENE, UniProtKB/TrEMBL
	B4DX42	ENTREZGENE, UniProtKB/TrEMBL
	B7Z1Q1	ENTREZGENE
	C9J792_HUMAN	UniProtKB/TrEMBL
	C9JJE2	ENTREZGENE
	E7ESU3	ENTREZGENE
	F8WEG7_HUMAN	UniProtKB/TrEMBL
	F8WEV5_HUMAN	UniProtKB/TrEMBL
	H7BZT1_HUMAN	UniProtKB/TrEMBL
	H7C0N4_HUMAN	UniProtKB/TrEMBL
	H7C561	ENTREZGENE, UniProtKB/TrEMBL
	L0R8E5_HUMAN	UniProtKB/TrEMBL
	Q14818	ENTREZGENE
	Q14819	ENTREZGENE
	Q14820_HUMAN	UniProtKB/TrEMBL
	Q15637	ENTREZGENE
	Q15913	ENTREZGENE
	Q8IY00	ENTREZGENE
	Q92744	ENTREZGENE
	Q92745	ENTREZGENE
	Q969H7	ENTREZGENE
	Q9BW01	ENTREZGENE
	Q9UEI0	ENTREZGENE
	SF01_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B7Z1Q1	UniProtKB/Swiss-Prot
	C9JJE2	UniProtKB/Swiss-Prot
	E7ESU3	UniProtKB/TrEMBL
	Q14818	UniProtKB/Swiss-Prot
	Q14819	UniProtKB/Swiss-Prot
	Q15913	UniProtKB/Swiss-Prot
	Q8IY00	UniProtKB/Swiss-Prot
	Q92744	UniProtKB/Swiss-Prot
	Q92745	UniProtKB/Swiss-Prot
	Q969H7	UniProtKB/Swiss-Prot
	Q9BW01	UniProtKB/Swiss-Prot
	Q9UEI0	UniProtKB/Swiss-Prot

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 Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

RGD Manual Annotations

Imported Human Phenotype Annotations - ClinVar