FGR (FGR proto-oncogene, Src family tyrosine kinase)

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Gene: FGR (FGR proto-oncogene, Src family tyrosine kinase) Homo sapiens

Analyze

Symbol:

FGR

Name:

FGR proto-oncogene, Src family tyrosine kinase

RGD ID:

733253

HGNC Page

HGNC

Description:

Exhibits Fc-gamma receptor I complex binding activity; non-membrane spanning protein tyrosine kinase activity; and phosphotyrosine residue binding activity. Involved in several processes, including integrin-mediated signaling pathway; positive regulation of phosphatidylinositol 3-kinase signaling; and protein phosphorylation. Localizes to aggresome and plasma membrane. Colocalizes with cytoskeleton.

Type:

protein-coding

RefSeq Status:

REVIEWED

Also known as:

c-fgr; c-fgr protooncogene; c-src-2 proto-oncogene; c-src2; feline Gardner-Rasheed sarcoma viral oncogene homolog; FLJ43153; Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog; MGC75096; p55-c-fgr protein; p55-Fgr; p55c-fgr; p58-Fgr; p58c-fgr; proto-oncogene c-Fgr; proto-oncogene tyrosine-protein kinase FGR; SRC2; tyrosine-protein kinase Fgr; v-fgr feline Gardner-Rasheed sarcoma viral oncogene homolog

RGD Orthologs

Mouse

Rat

Chinchilla

Bonobo

Dog

Squirrel

Pig

Green Monkey

Naked Mole-Rat

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38.p13 Ensembl	1	27,612,064 - 27,635,185 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38	1	27,612,064 - 27,635,561 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh37	1	27,938,575 - 27,961,696 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	27,811,387 - 27,834,314 (-)	NCBI	NCBI36		hg18	NCBI36
Build 34	1	27,622,952 - 27,634,715	NCBI
Celera	1	26,334,465 - 26,357,390 (-)	NCBI
Cytogenetic Map	1	p35.3	NCBI
HuRef	1	26,195,016 - 26,217,930 (-)	NCBI		HuRef
CHM1_1	1	28,054,060 - 28,076,993 (-)	NCBI		CHM1_1

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Experimental Liver Cirrhosis (EXP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,1-dichloroethene (ISO)

1-naphthyl isothiocyanate (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP)

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

2,4-dinitrotoluene (ISO)

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

4,4'-diaminodiphenylmethane (ISO)

4-hydroxynon-2-enal (ISO)

6-propyl-2-thiouracil (ISO)

acetamide (ISO)

acetylsalicylic acid (EXP)

aflatoxin B1 (EXP)

aflatoxin B2 (EXP)

all-trans-retinoic acid (EXP)

ammonium chloride (ISO)

antirheumatic drug (EXP)

arsenous acid (EXP)

benzalkonium chloride (ISO)

benzo[a]pyrene (EXP,ISO)

bis(2-chloroethyl) sulfide (ISO)

bisphenol A (EXP,ISO)

bosutinib (ISO)

bromobenzene (ISO)

buta-1,3-diene (ISO)

butan-1-ol (EXP)

cadmium dichloride (EXP)

carbon nanotube (ISO)

chloroprene (ISO)

chlorpromazine (ISO)

cisplatin (EXP)

cyclosporin A (ISO)

dexamethasone (EXP)

diarsenic trioxide (EXP)

dichlorine (ISO)

diethyl maleate (ISO)

diethylstilbestrol (EXP)

endosulfan (ISO)

fenofibrate (ISO)

genistein (ISO)

hypochlorous acid (ISO)

indometacin (EXP)

leflunomide (ISO)

lipopolysaccharide (ISO)

metformin (ISO)

N-formyl-L-methionyl-L-leucyl-L-phenylalanine (EXP)

N-nitrosodimethylamine (ISO)

nickel atom (EXP)

nickel dichloride (ISO)

ozone (ISO)

paracetamol (EXP)

perfluorooctanoic acid (ISO)

phosphatidic acid (EXP)

ponatinib (EXP)

resveratrol (ISO)

SB 431542 (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

sodium fluoride (ISO)

tamibarotene (EXP)

Tesaglitazar (ISO)

titanium dioxide (ISO)

troglitazone (ISO)

tungsten (ISO)

valproic acid (EXP)

vincristine (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

bone mineralization (IEA,ISO)

cell differentiation (IBA)

defense response to Gram-positive bacterium (ISO,ISS)

Fc-gamma receptor signaling pathway involved in phagocytosis (TAS)

immune response-regulating cell surface receptor signaling pathway (TAS)

innate immune response (IBA)

integrin-mediated signaling pathway (IBA,IMP,ISO,ISS)

negative regulation of inflammatory response to antigenic stimulus (TAS)

negative regulation of natural killer cell activation (IEA,ISO)

neutrophil degranulation (TAS)

peptidyl-tyrosine phosphorylation (IDA,IEA,ISO)

positive regulation of cell migration (ISO,ISS)

positive regulation of cytokine production (ISO,ISS)

positive regulation of mast cell degranulation (ISO,ISS)

positive regulation of phosphatidylinositol 3-kinase activity (IMP)

positive regulation of phosphatidylinositol 3-kinase signaling (IMP)

protein autophosphorylation (IDA)

protein phosphorylation (TAS)

regulation of cell shape (ISO,ISS)

regulation of innate immune response (ISO,ISS)

regulation of phagocytosis (ISO,ISS)

regulation of protein kinase activity (ISO,ISS)

response to virus (TAS)

skeletal system morphogenesis (IEA,ISO)

transmembrane receptor protein tyrosine kinase signaling pathway (IBA)

Cellular Component

actin cytoskeleton (ISS)

aggresome (IDA)

cytoskeleton (IDA)

cytosol (ISO,TAS)

extracellular exosome (HDA)

extracellular region (TAS)

extrinsic component of cytoplasmic side of plasma membrane (IBA)

mitochondrial inner membrane (IEA)

mitochondrial intermembrane space (IEA)

plasma membrane (IDA,ISO,ISS)

ruffle membrane (ISS)

secretory granule lumen (TAS)

Molecular Function

ATP binding (IEA)

Fc-gamma receptor I complex binding (IDA)

immunoglobulin receptor binding (ISO,ISS)

non-membrane spanning protein tyrosine kinase activity (IBA,IDA,IEA,ISO)

phosphotyrosine residue binding (IPI,ISO,ISS)

protein binding (IPI,ISO)

protein kinase binding (ISO,ISS)

protein tyrosine kinase activity (IBA,IDA,ISO)

signaling receptor binding (IBA)

transmembrane receptor protein tyrosine kinase activity (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

eicosanoid signaling pathway (EXP)

ephrin - ephrin receptor bidirectional signaling axis (EXP)

glypican signaling pathway (EXP)

phosphatidylinositol 3-kinase class I signaling pathway (EXP)

platelet-derived growth factor signaling pathway (EXP)

References

References - curated


1.	GOA_HUMAN data from the GO Consortium
2.	Pipeline to import Pathway Interaction Database annotations from NCI into RGD
3.	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4.	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1339476	PMID:1373875	PMID:1652975	PMID:1690869	PMID:1826268	PMID:1847500	PMID:2154410	PMID:2181286	PMID:2581127	PMID:2852026	PMID:2995972	PMID:3003578
PMID:3023853	PMID:3275868	PMID:3330776	PMID:3922831	PMID:7515063	PMID:7519620	PMID:7565724	PMID:7678701	PMID:7721825	PMID:7726865	PMID:7812001	PMID:8313462
PMID:8327512	PMID:8603737	PMID:8612628	PMID:8753773	PMID:8805332	PMID:8824280	PMID:8867673	PMID:9208935	PMID:10066823	PMID:10080533	PMID:10229804	PMID:10358777
PMID:10527858	PMID:10702640	PMID:10739672	PMID:10861086	PMID:10973280	PMID:11071635	PMID:11162638	PMID:11526478	PMID:11546677	PMID:11672534	PMID:11744621	PMID:11823534
PMID:11928806	PMID:12096713	PMID:12244095	PMID:12387730	PMID:12387813	PMID:12435267	PMID:12468645	PMID:12473651	PMID:12477932	PMID:14702039	PMID:15098032	PMID:15190072
PMID:15459198	PMID:15489334	PMID:15536084	PMID:15561106	PMID:15707590	PMID:15723811	PMID:15919723	PMID:16273093	PMID:16344560	PMID:16684964	PMID:16710414	PMID:16921024
PMID:17164290	PMID:17845055	PMID:20056178	PMID:20098747	PMID:20458337	PMID:20624904	PMID:20804422	PMID:21300758	PMID:21873635	PMID:21988832	PMID:22745667	PMID:22939624
PMID:22973453	PMID:22974441	PMID:23131831	PMID:23867815	PMID:23896410	PMID:24162774	PMID:24658140	PMID:24728074	PMID:24860872	PMID:25402006	PMID:25972488	PMID:26186194
PMID:27324824	PMID:28514442	PMID:28585144	PMID:29568343	PMID:29763550	PMID:29845934	PMID:30352950	PMID:31586073	PMID:31790499	PMID:31980649

Genomics

Comparative Map Data

FGR
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38.p13 Ensembl	1	27,612,064 - 27,635,185 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38	1	27,612,064 - 27,635,561 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh37	1	27,938,575 - 27,961,696 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	27,811,387 - 27,834,314 (-)	NCBI	NCBI36		hg18	NCBI36
Build 34	1	27,622,952 - 27,634,715	NCBI
Celera	1	26,334,465 - 26,357,390 (-)	NCBI
Cytogenetic Map	1	p35.3	NCBI
HuRef	1	26,195,016 - 26,217,930 (-)	NCBI		HuRef
CHM1_1	1	28,054,060 - 28,076,993 (-)	NCBI		CHM1_1

Fgr
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	4	132,701,406 - 132,729,204 (+)	NCBI	GRCm39		mm39
GRCm39 Ensembl	4	132,701,406 - 132,729,221 (+)	Ensembl
GRCm38	4	132,974,095 - 133,001,893 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	4	132,974,095 - 133,001,910 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	4	132,530,010 - 132,557,808 (+)	NCBI	GRCm37		mm9	NCBIm37
MGSCv36	4	132,246,204 - 132,273,882 (+)	NCBI			mm8
Celera	4	131,136,566 - 131,164,622 (+)	NCBI		Celera
Cytogenetic Map	4	D2.3	NCBI
cM Map	4	66.11	NCBI

Fgr
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mRatBN7.2	5	145,189,814 - 145,219,571 (+)	NCBI
Rnor_6.0 Ensembl	5	151,172,206 - 151,199,745 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_6.0	5	151,172,189 - 151,199,746 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_5.0	5	154,839,086 - 154,866,424 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	5	152,119,455 - 152,147,057 (-)	NCBI	RGSC3.4		rn4	RGSC3.4
RGSC_v3.1	5	152,129,494 - 152,157,096 (-)	NCBI
Celera	5	143,612,003 - 143,639,441 (+)	NCBI		Celera
RH 3.4 Map	5	977.8	RGD
Cytogenetic Map	5	q36	NCBI

Fgr
(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_004955452	6,841,802 - 6,863,542 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955452	6,840,274 - 6,863,460 (-)	NCBI	ChiLan1.0	ChiLan1.0

FGR
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
PanPan1.1	1	27,918,758 - 27,941,678 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	1	27,918,758 - 27,941,678 (-)	Ensembl	panpan1.1		panPan2
Mhudiblu_PPA_v0	1	26,872,781 - 26,895,751 (-)	NCBI	Mhudiblu_PPA_v0		panPan3

FGR
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1 Ensembl	2	72,680,675 - 72,690,251 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
CanFam3.1	2	72,678,858 - 72,692,417 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1

Fgr
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
SpeTri2.0	NW_004936474	11,897,998 - 11,919,153 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

FGR
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	84,809,542 - 84,830,361 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	84,809,534 - 84,830,401 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	78,326,176 - 78,358,345 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

FGR
(Chlorocebus sabaeus - African green monkey)

Vervet Assembly	Chr	Position (strand)	Source	Genome Browsers
Vervet Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	20	105,155,223 - 105,178,813 (+)	NCBI
ChlSab1.1 Ensembl	20	105,165,043 - 105,179,067 (+)	Ensembl

Fgr
(Heterocephalus glaber - naked mole-rat)

Molerat Assembly	Chr	Position (strand)	Source	Genome Browsers
Molerat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla 1.0	NW_004624764	11,482,719 - 11,513,215 (-)	NCBI

Position Markers

SHGC-74510

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,948,252 - 27,948,501	UniSTS	GRCh37
Build 36	1	27,820,839 - 27,821,088	RGD	NCBI36
Celera	1	26,343,917 - 26,344,166	RGD
Cytogenetic Map	1	p36.2-p36.1	UniSTS
HuRef	1	26,204,459 - 26,204,708	UniSTS
TNG Radiation Hybrid Map	1	12556.0	UniSTS
GeneMap99-GB4 RH Map	1	95.57	UniSTS

SHGC-74489

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,938,871 - 27,939,058	UniSTS	GRCh37
Build 36	1	27,811,458 - 27,811,645	RGD	NCBI36
Celera	1	26,334,536 - 26,334,723	RGD
Cytogenetic Map	1	p36.2-p36.1	UniSTS
HuRef	1	26,195,087 - 26,195,274	UniSTS
TNG Radiation Hybrid Map	1	12564.0	UniSTS
GeneMap99-GB4 RH Map	1	94.47	UniSTS

GDB:549146

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,939,416 - 27,939,632	UniSTS	GRCh37
Build 36	1	27,812,003 - 27,812,219	RGD	NCBI36
Celera	1	26,335,081 - 26,335,297	RGD
Cytogenetic Map	1	p36.2-p36.1	UniSTS
HuRef	1	26,195,632 - 26,195,848	UniSTS

UniSTS:24107

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,953,861 - 27,954,165	UniSTS	GRCh37
Build 36	1	27,826,448 - 27,826,752	RGD	NCBI36
Celera	1	26,349,526 - 26,349,828	RGD
HuRef	1	26,210,068 - 26,210,370	UniSTS

SHGC-74509

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,951,792 - 27,951,985	UniSTS	GRCh37
Build 36	1	27,824,379 - 27,824,572	RGD	NCBI36
Celera	1	26,347,457 - 26,347,650	RGD
Cytogenetic Map	1	p36.2-p36.1	UniSTS
HuRef	1	26,207,999 - 26,208,192	UniSTS
TNG Radiation Hybrid Map	1	12552.0	UniSTS
GeneMap99-GB4 RH Map	1	95.57	UniSTS

SHGC-6996

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,954,970 - 27,955,106	UniSTS	GRCh37
Build 36	1	27,827,557 - 27,827,693	RGD	NCBI36
Celera	1	26,350,633 - 26,350,769	RGD
Cytogenetic Map	1	p36.2-p36.1	UniSTS
HuRef	1	26,211,175 - 26,211,311	UniSTS

FGR__5988

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	27,938,611 - 27,939,481	UniSTS	GRCh37
Build 36	1	27,811,198 - 27,812,068	RGD	NCBI36
Celera	1	26,334,276 - 26,335,146	RGD
HuRef	1	26,194,827 - 26,195,697	UniSTS

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2473
Count of miRNA genes:	692
Interacting mature miRNAs:	799
Transcripts:	ENST00000374003, ENST00000374004, ENST00000374005, ENST00000399173, ENST00000457296, ENST00000468038, ENST00000475472, ENST00000545953
Prediction methods:	Microtar, 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.

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

adipose tissue

appendage

entire extraembryonic component

High

161

Medium

627

1146

515

1566

1407

285

650

121

418

1041

1101

708

Low

1689

1671

1176

510

153

390

2733

1845

2977

255

926

358

120

103

2066

Below cutoff

148

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001042729	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001042747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_005248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006710452	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011541010	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011541011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011541012	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011541013	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011541014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017000673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017000674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_946583	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AH001461	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH002726	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK125143	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK130188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK304846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL031729	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC064382	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI771758	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ448283	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX495937	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CQ834776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA139476	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA952771	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA960178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	K03219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M19721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M19722	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M27454	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X52205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X52206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X52207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X52208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Z13983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Z13989	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Reference Sequences

RefSeq Acc Id:

ENST00000374003 ⟹ ENSP00000363115

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,612,669 - 27,626,569 (-)	Ensembl

RefSeq Acc Id:

ENST00000374004 ⟹ ENSP00000363116

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,612,300 - 27,624,062 (-)	Ensembl

RefSeq Acc Id:

ENST00000374005 ⟹ ENSP00000363117

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,612,064 - 27,635,185 (-)	Ensembl

RefSeq Acc Id:

ENST00000399173 ⟹ ENSP00000382126

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,612,292 - 27,626,240 (-)	Ensembl

RefSeq Acc Id:

ENST00000457296 ⟹ ENSP00000407670

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,615,514 - 27,626,135 (-)	Ensembl

RefSeq Acc Id:

ENST00000468038

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,623,407 - 27,626,240 (-)	Ensembl

RefSeq Acc Id:

ENST00000475472

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	1	27,623,384 - 27,635,134 (-)	Ensembl

RefSeq Acc Id:

NM_001042729 ⟹ NP_001036194

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,064 - 27,626,597 (-)	NCBI
GRCh37	1	27,938,800 - 27,961,727 (-)	ENTREZGENE
Build 36	1	27,811,387 - 27,825,693 (-)	NCBI Archive
HuRef	1	26,195,016 - 26,217,930 (-)	ENTREZGENE
CHM1_1	1	28,054,060 - 28,068,372 (-)	NCBI

Sequence:

show sequence

TACACACATGAGAGATCACTTAGAGCAAAGGGTGAGAGGGGCAGGTGGGGCTAGGGTGGAGACC
AAAGCACTGATGTGACGGAACCATCAGCCAGGCAACTGGACCTGGTGGATCCAGGAAGACTTTC
TGGAAGAGGTCTCTGACCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGC
CTAAGGGCAGGGAACCTGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGC
CAAGGAGGATGCTGGCCTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCT
GACCCCACTAAGGCCCGGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCT
CTCAGGCCATCAACCCTGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGT
GACCCTGTTCATTGCCCTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAG
GGCGAGAAGTTCCACATCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCT
CCGGAAAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGA
GTGGTACTTTGGAAAGATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCC
CAGGGGGCCTTTCTCATTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGG
ACTGGGATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGG
CTACTACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAG
GTGAATGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGG
GCCTGGCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCAC
CGGCTGCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACG
CTGAAGCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGC
GGCACGACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGA
GTTCATGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTG
CCCCAATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGAACT
ACATTCACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGC
AGACTTTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTC
CCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGT
GGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCATGAA
TAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCA
GCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCG
AGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGA
TCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCC
AGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGG
ACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCC
CAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCT
ACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTA
TAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCA
CTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAA
GTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGT
CTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGT
GTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGAATCCTCAAACCATGAAAAAAAA
AAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001042747 ⟹ NP_001036212

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,064 - 27,626,251 (-)	NCBI
GRCh37	1	27,938,800 - 27,961,727 (-)	ENTREZGENE
Build 36	1	27,811,387 - 27,825,338 (-)	NCBI Archive
HuRef	1	26,195,016 - 26,217,930 (-)	ENTREZGENE
CHM1_1	1	28,054,060 - 28,068,017 (-)	NCBI

Sequence:

show sequence

CTCTGAGTGTTGCAATGGCAATGTTTCTGGCAGGGTGTGGGGGACCCTTGCTCAATGACCTCCT
GCCCTGTTGCTCAGAGGATACCGCTGCCAGAAAAGGGTTGGCTCATTGTGGGGCTTCCCAAGGT
ACTCTGGTAGCCCCAGCTTCTGACCTGGTCCTTTCTCTGGTATGGGGATAGGAGGAGAGCTCCG
GAGGTCTCTGACCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAG
GGCAGGGAACCTGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGG
AGGATGCTGGCCTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCC
CACTAAGGCCCGGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAG
GCCATCAACCCTGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGTGACCC
TGTTCATTGCCCTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAGGGCGA
GAAGTTCCACATCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGA
AAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGGT
ACTTTGGAAAGATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGG
GGCCTTTCTCATTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGG
GATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACT
ACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAA
TGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTG
GCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCT
GCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAA
GCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCAC
GACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCA
TGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCA
ATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGAACTACATT
CACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGCAGACT
TTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTCCCCAT
CAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGTGGTCC
TTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCATGAATAAAC
GGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCAGCATC
CCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCGAGTAC
CTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGATCAGA
CATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCCAGAGC
TGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGGACGTG
GCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCCCAGAG
CTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCTACATG
CCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTATAAAA
CTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCACTCTA
GTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAAGTCAG
GAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGTCTGGG
CCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGTGTTGG
TTTATTGATTCTGTAAATAAGTAAAATGACAATATGAATCCTCAAACCATGAAAAAAAAAAAAA
AAAAA

hide sequence

RefSeq Acc Id:

NM_005248 ⟹ NP_005239

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,064 - 27,635,185 (-)	NCBI
GRCh37	1	27,938,800 - 27,961,727 (-)	ENTREZGENE
Build 36	1	27,811,387 - 27,834,314 (-)	NCBI Archive
HuRef	1	26,195,016 - 26,217,930 (-)	ENTREZGENE
CHM1_1	1	28,054,060 - 28,076,993 (-)	NCBI

Sequence:

show sequence

AATAAGAGAAGTCCGAGGCGGCTTCCTCCTCCCTGCCCAGCAGGGGCGGCGGTCAGAGGCGGGC
AGCACCCCAGTTCTCCCCGCACGCCGGCACTCGCGGCTGCTGGAGCCCCGGCTGGCTCACCCCG
GGGCCGGGCAGAATTGGGCTCCAGGTCTCTGACCCCTCCCAAGGATCATGCCGCAGCCCCACTG
ACCCAGGAGTAGGGGCCTAAGGGCAGGGAACCTGGAATGGGCTGTGTGTTCTGCAAGAAATTGG
AGCCGGTGGCCACGGCCAAGGAGGATGCTGGCCTGGAAGGGGACTTCAGAAGCTACGGGGCAGC
AGACCACTATGGGCCTGACCCCACTAAGGCCCGGCCTGCATCCTCATTTGCCCACATCCCCAAC
TACAGCAACTTCTCCTCTCAGGCCATCAACCCTGGCTTCCTTGATAGTGGCACCATCAGGGGTG
TGTCAGGGATTGGGGTGACCCTGTTCATTGCCCTGTATGACTATGAGGCTCGAACTGAGGATGA
CCTCACCTTCACCAAGGGCGAGAAGTTCCACATCCTGAACAATACTGAAGGTGACTGGTGGGAG
GCTCGGTCTCTCAGCTCCGGAAAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACT
CAATCCAAGCTGAAGAGTGGTACTTTGGAAAGATTGGGAGAAAGGATGCAGAGAGGCAGCTGCT
TTCACCAGGCAACCCCCAGGGGGCCTTTCTCATTCGGGAAAGCGAGACCACCAAAGGTGCCTAC
TCCCTGTCCATCCGGGACTGGGATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATCCGCA
AACTGGACATGGGCGGCTACTACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGCTGGT
GCAGCACTACATGGAGGTGAATGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCATCATG
AAGCCGCAGACGCTGGGCCTGGCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACGCTGG
AGCGCCGGCTGGGCACCGGCTGCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCACTAA
GGTGGCGGTGAAGACGCTGAAGCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAG
GTCATGAAGCTGCTGCGGCACGACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAGCCCA
TCTACATCGTGACCGAGTTCATGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAGAGGG
CCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGCCTAC
ATGGAACGCATGAACTACATTCACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAGCGGC
TGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACCCCTG
CCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTCACC
ATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGAATCC
CCTACCCAGGCATGAATAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGCCGTG
CCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCCGGAG
GAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAACCAC
AGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCCACCA
GTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATAGAGT
CCTAGCATCACCGAGGACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTACAGAT
GGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTTCCTT
TTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTCAGAC
CTTGTCTAGTTATTTATAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTTCCTA
CTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTCTTGT
GTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATGCAGT
GGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACCTCTC
TGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGAATCCTC
AAACCATGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_006710452 ⟹ XP_006710515

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,144 (-)	NCBI

Sequence:

show sequence

AGTTCTCCCCGCACGCCGGCACTCGCGGCTGCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGG
CAGAATTGGGCTCCAGAGACAGGGTCTTACTCTGTCTCCCAGGCTGGAGTGCAGCGGTGCAATC
ACAGCTCCTGCAGCCTCGAACTCCCAGGCTTAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGC
TGGGACTACAGGTCTCTGACCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGG
GGCCTAAGGGCAGGGAACCTGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCAC
GGCCAAGGAGGATGCTGGCCTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGG
CCTGACCCCACTAAGGCCCGGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCT
CCTCTCAGGCCATCAACCCTGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGG
GGTGACCCTGTTCATTGCCCTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACC
AAGGGCGAGAAGTTCCACATCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCA
GCTCCGGAAAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGA
AGAGTGGTACTTTGGAAAGATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAAC
CCCCAGGGGGCCTTTCTCATTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCC
GGGACTGGGATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGG
CGGCTACTACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATG
GAGGTGAATGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGC
TGGGCCTGGCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGG
CACCGGCTGCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAG
ACGCTGAAGCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGC
TGCGGCACGACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGAC
CGAGTTCATGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGG
CTGCCCCAATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGA
ACTACATTCACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGAT
CGCAGACTTTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAG
TTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACG
TGTGGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCAT
GAATAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGC
CCAGCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCT
TCGAGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGG
GGATCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATC
CCCAGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCG
AGGACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAG
GCCCAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCC
CCTACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTAT
TTATAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATC
TCACTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTAC
AAAGTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGG
GGTCTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTA
TGTGTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGAATCCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_011541010 ⟹ XP_011539312

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,561 (-)	NCBI

Sequence:

show sequence

GACAGCAGTCTGAAGTCAACTGGCTGTGAGAACTCGAGTAAGGCCAGTCCCGATCTGGTCCTCA
GTGATGGAGAAAAGCCCCTCTTAACCTCCAATTCAATGATCCTAAAAGAGCAGGTCTCTGACCC
CTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGCAGGGAACCTGG
AATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGGAGGATGCTGGCCTG
GAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCCCACTAAGGCCCGGC
CTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAGGCCATCAACCCTGG
CTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGTGACCCTGTTCATTGCCCTG
TATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAGGGCGAGAAGTTCCACATCC
TGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGAAAAACTGGCTGCAT
TCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGGTACTTTGGAAAGATT
GGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCATTC
GGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAGAGG
CGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACACGG
GTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGTGCA
ACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGCCTG
GGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGATGTG
TGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCATGT
CCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGTGCA
GCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGGCAGC
TTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGG
CAGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGAACTACATTCACCGCGACCTGAG
GGCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGT
CTCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCC
CAGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCT
CACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAA
CAGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCA
TGGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCT
GGAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGG
GCATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGC
CCCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACC
ACCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCC
GCTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCT
CACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCC
CTCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAG
AATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCT
GGACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGG
AGAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGT
AAATAAGTAAAATGACAATATGAATCCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_011541011 ⟹ XP_011539313

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,187 (-)	NCBI

Sequence:

show sequence

TCCCTGCCCAGCAGGGGCGGCGGTCAGAGGCGGGCAGCACCCCAGTTCTCCCCGCACGCCGGCA
CTCGCGGCTGCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGGCAGAATTGGGCTCCAGGTCTC
TGACCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGCAGGGA
ACCTGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGGAGGATGCT
GGCCTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCCCACTAAGG
CCCGGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAGGCCATCAA
CCCTGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGTGAAGGTGACTGGTGGGAGGCTC
GGTCTCTCAGCTCCGGAAAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACTCAAT
CCAAGCTGAAGAGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAGAGGCGATCATGT
GAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACACGGGTTCAGTTC
AACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGTGCAACCTGCTCA
TCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGCCTGGGAGATCAG
CCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGATGTGTGGCTGGGC
ACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCATGTCCCCGAAGG
CCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGTGCAGCTGTACGC
CGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGGCAGCTTGCTGGAT
TTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGCAGCCCAGG
TAGCTGAGGGCATGGCCTACATGGAACGCATGAACTACATTCACCGCGACCTGAGGGCAGCCAA
CATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGTCTCATCAAG
GACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTG
CCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTCACTGAGCT
CATCACCAAGGGCCGAATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAACAGGTGGAG
CAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCATGGAACAGA
CCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTGGAGGACTA
CTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGGCATCAACC
CTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCCCCCAGGCT
GGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACCACCTAGGGC
AACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCGCTCTGGCC
CCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTCACTCCATC
CCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCCCTCACTTCT
CTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGAATTTCCCT
TCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTGGACCCCTT
TCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGAGAAGGTTG
CAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTAAATAAGTA
AAATGACAATATGAATCCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_011541012 ⟹ XP_011539314

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,184 (-)	NCBI

Sequence:

show sequence

CTGCCCAGCAGGGGCGGCGGTCAGAGGCGGGCAGCACCCCAGTTCTCCCCGCACGCCGGCACTC
GCGGCTGCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGGCAGAATTGGGCTCCAGGTCTCTGA
CCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGCAGGGAACC
TGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGGAGGATGCTGGC
CTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCCCACTAAGGCCC
GGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAGGCCATCAACCC
TGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGTGACCCTGTTCATTGCC
CTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAGGGCGAGAAGTTCCACA
TCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGAAAAACTGGCTG
CATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGGTACTTTGGAAAG
ATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCA
TTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAG
AGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACA
CGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGT
GCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGC
CTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGAT
GTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCA
TGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGT
GCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGGC
AGCTTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACA
TGGCAGCCCAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGA
TTCACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCC
GAATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACAT
GCCGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGAC
CCGGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTG
AACCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGG
CCACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCA
TAGAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTT
ACAGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTC
TTCCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGC
TCAGACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCT
TTCCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTC
TCTTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGA
TGCAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCA
CCTCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGA
ATCCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_011541013 ⟹ XP_011539315

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,613,283 - 27,635,184 (-)	NCBI

Sequence:

show sequence

CTGCCCAGCAGGGGCGGCGGTCAGAGGCGGGCAGCACCCCAGTTCTCCCCGCACGCCGGCACTC
GCGGCTGCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGGCAGAATTGGGCTCCAGGTCTCTGA
CCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGCAGGGAACC
TGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGGAGGATGCTGGC
CTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCCCACTAAGGCCC
GGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAGGCCATCAACCC
TGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGTGACCCTGTTCATTGCC
CTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAGGGCGAGAAGTTCCACA
TCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGAAAAACTGGCTG
CATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGGTACTTTGGAAAG
ATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCA
TTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAG
AGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACA
CGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGT
GCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGC
CTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGAT
GTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCA
TGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGT
GCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGCT
TGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGC
AGCCCAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTCA
CCATCAAGTCA

hide sequence

RefSeq Acc Id:

XM_011541014 ⟹ XP_011539316

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,619,195 (-)	NCBI

Sequence:

show sequence

TAATTAAAAATTTTTAAAAAAGCTATATAGACGGTTAAGGAAGAGAGTGGAGAGTGCAAAAGGT
TGGCCCTAGGACCCCACTTTGGGGAAAGCTGCCCTCGAAGGAGAAGGAGCCATTGGAGAAGAGA
GGAAATCCAGACCAGGCCAAGTCAGAACAACCGAGAGAGCGGAGAAGCTTCAGGAAACAAGAGA
GGGCGTGTCAGAGGCTACCGCTGGATTTGGCAGTGGGGGTGACCTTGGTGGTACTTTGGAAAGA
TTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCAT
TCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAGA
GGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACAC
GGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGTG
CAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGCC
TGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGATG
TGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCAT
GTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGTG
CAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGGCA
GCTTGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACAT
GGCAGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGAACTACATTCACCGCGACCTG
AGGGCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGC
GTCTCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGC
CCCAGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTG
CTCACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGG
AACAGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGC
CATGGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTC
CTGGAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCC
GGGCATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAA
GCCCCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACA
CCACCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCAT
CCGCTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTT
CTCACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTATAAAACTGTATGTACCT
CCCTCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCA
AGAATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGG
CTGGACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAG
GGAGAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCT
GTAAATAAGTAAAATGACAATATGAATCCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_017000673 ⟹ XP_016856162

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,178 (-)	NCBI

Sequence:

show sequence

AGCAGGGGCGGCGGTCAGAGGCGGGCAGCACCCCAGTTCTCCCCGCACGCCGGCACTCGCGGCT
GCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGGCAGAATTGGGCTCCAGGTCTCTGACCCCTC
CCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGTGAAGGTGACTGGTG
GGAGGCTCGGTCTCTCAGCTCCGGAAAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTT
GACTCAATCCAAGCTGAAGAGTGGTACTTTGGAAAGATTGGGAGAAAGGATGCAGAGAGGCAGC
TGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCATTCGGGAAAGCGAGACCACCAAAGGTGC
CTACTCCCTGTCCATCCGGGACTGGGATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATC
CGCAAACTGGACATGGGCGGCTACTACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGC
TGGTGCAGCACTACATGGAGGTGAATGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCAT
CATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACG
CTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCA
CTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGC
GCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAG
CCCATCTACATCGTGACCGAGTTCATGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAG
AGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGC
CTACATGGAACGCATGAACTACATTCACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAG
CGGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACC
CCTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATT
CACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGA
ATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGC
CGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCC
GGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAA
CCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCC
ACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATA
GAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTAC
AGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTT
CCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTC
AGACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTT
CCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTC
TTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATG
CAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACC
TCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGAAT
CCTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XM_017000674 ⟹ XP_016856163

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,217 (-)	NCBI

Sequence:

show sequence

CAATAAGAGAAGTCCGAGGCGGCTTCCTCCTCCCTGCCCAGCAGGGGCGGCGGTCAGAGGCGGG
CAGCACCCCAGTTCTCCCCGCACGCCGGCACTCGCGGCTGCTGGAGCCCCGGCTGGCTCACCCC
GGGGCCGGGCAGAATTGGGCTCCAGGTCTCTGACCCCTCCCAAGGATCATGCCGCAGCCCCACT
GACCCAGGAGTAGGGGCCTAAGGGTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGA
AAAACTGGCTGCATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGCC
TACTCCCTGTCCATCCGGGACTGGGATCAGACCAGAGGCGATCATGTGAAGCATTACAAGATCC
GCAAACTGGACATGGGCGGCTACTACATCACCACACGGGTTCAGTTCAACTCGGTGCAGGAGCT
GGTGCAGCACTACATGGAGGTGAATGACGGGCTGTGCAACCTGCTCATCGCGCCCTGCACCATC
ATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGCCTGGGAGATCAGCCGCAGCTCCATCACGC
TGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGATGTGTGGCTGGGCACGTGGAACGGCAGCAC
TAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCATGTCCCCGAAGGCCTTCCTGGAGGAGGCG
CAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGTGCAGCTGTACGCCGTGGTGTCGGAGGAGC
CCATCTACATCGTGACCGAGTTCATGTGTCACGGCAGCTTGCTGGATTTTCTCAAGAACCCAGA
GGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGCAGCCCAGGTAGCTGAGGGCATGGCC
TACATGGAACGCATGAACTACATTCACCGCGACCTGAGGGCAGCCAACATCCTGGTTGGGGAGC
GGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGTCTCATCAAGGACGATGAGTACAACCC
CTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCCAGAAGCTGCCCTCTTTGGCAGATTC
ACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTCACTGAGCTCATCACCAAGGGCCGAA
TCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAACAGGTGGAGCAGGGCTACCACATGCC
GTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCATGGAACAGACCTGGCGTCTGGACCCG
GAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTGGAGGACTACTTCACCTCCGCTGAAC
CACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGGCATCAACCCTCTCTGGCGGTGGCCA
CCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCCCCCAGGCTGGCTTAGAACCCCATAG
AGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACCACCTAGGGCAACCTACTTGTTTTACA
GATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCGCTCTGGCCCCAAGCACTATTTCTTC
CTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTCACTCCATCCCCACCCAAAGTGCTCA
GACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCCCTCACTTCTCTCCTATCACTGCTTTC
CTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGAATTTCCCTTCTACCCTCTATTCTCT
TGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTGGACCCCTTTCCTGCTGGGTGGATGC
AGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGAGAAGGTTGCAGAGCACTTCCCACCT
CTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTAAATAAGTAAAATGACAATATGAATC
CTCAAACCATGAAA

hide sequence

RefSeq Acc Id:

XR_946583

RefSeq Status:

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,612,289 - 27,635,184 (-)	NCBI

Sequence:

show sequence

CTGCCCAGCAGGGGCGGCGGTCAGAGGCGGGCAGCACCCCAGTTCTCCCCGCACGCCGGCACTC
GCGGCTGCTGGAGCCCCGGCTGGCTCACCCCGGGGCCGGGCAGAATTGGGCTCCAGGTCTCTGA
CCCCTCCCAAGGATCATGCCGCAGCCCCACTGACCCAGGAGTAGGGGCCTAAGGGCAGGGAACC
TGGAATGGGCTGTGTGTTCTGCAAGAAATTGGAGCCGGTGGCCACGGCCAAGGAGGATGCTGGC
CTGGAAGGGGACTTCAGAAGCTACGGGGCAGCAGACCACTATGGGCCTGACCCCACTAAGGCCC
GGCCTGCATCCTCATTTGCCCACATCCCCAACTACAGCAACTTCTCCTCTCAGGCCATCAACCC
TGGCTTCCTTGATAGTGGCACCATCAGGGGTGTGTCAGGGATTGGGGTGACCCTGTTCATTGCC
CTGTATGACTATGAGGCTCGAACTGAGGATGACCTCACCTTCACCAAGGGCGAGAAGTTCCACA
TCCTGAACAATACTGAAGGTGACTGGTGGGAGGCTCGGTCTCTCAGCTCCGGAAAAACTGGCTG
CATTCCCAGCAACTACGTGGCCCCTGTTGACTCAATCCAAGCTGAAGAGTGGTACTTTGGAAAG
ATTGGGAGAAAGGATGCAGAGAGGCAGCTGCTTTCACCAGGCAACCCCCAGGGGGCCTTTCTCA
TTCGGGAAAGCGAGACCACCAAAGGTGCCTACTCCCTGTCCATCCGGGACTGGGATCAGACCAG
AGGCGATCATGTGAAGCATTACAAGATCCGCAAACTGGACATGGGCGGCTACTACATCACCACA
CGGGTTCAGTTCAACTCGGTGCAGGAGCTGGTGCAGCACTACATGGAGGTGAATGACGGGCTGT
GCAACCTGCTCATCGCGCCCTGCACCATCATGAAGCCGCAGACGCTGGGCCTGGCCAAGGACGC
CTGGGAGATCAGCCGCAGCTCCATCACGCTGGAGCGCCGGCTGGGCACCGGCTGCTTCGGGGAT
GTGTGGCTGGGCACGTGGAACGGCAGCACTAAGGTGGCGGTGAAGACGCTGAAGCCGGGCACCA
TGTCCCCGAAGGCCTTCCTGGAGGAGGCGCAGGTCATGAAGCTGCTGCGGCACGACAAGCTGGT
GCAGCTGTACGCCGTGGTGTCGGAGGAGCCCATCTACATCGTGACCGAGTTCATGTGTCACGCT
TGCTGGATTTTCTCAAGAACCCAGAGGGCCAGGATTTGAGGCTGCCCCAATTGGTGGACATGGC
AGCCCAGGTAGCTGAGGGCATGGCCTACATGGAACGCATGAACTACATTCACCGCGACCTGAGG
GCAGCCAACATCCTGGTTGGGGAGCGGCTGGCGTGCAAGATCGCAGACTTTGGCTTGGCGCGTC
TCATCAAGGACGATGAGTACAACCCCTGCCAAGGTTCCAAGTTCCCCATCAAGTGGACAGCCCC
AGAAGCTGCCCTCTTTGGCAGATTCACCATCAAGTCAGACGTGTGGTCCTTTGGGATCCTGCTC
ACTGAGCTCATCACCAAGGGCCGAATCCCCTACCCAGGCATGAATAAACGGGAAGTGTTGGAAC
AGGTGGAGCAGGGCTACCACATGCCGTGCCCTCCAGGCTGCCCAGCATCCCTGTACGAGGCCAT
GGAACAGACCTGGCGTCTGGACCCGGAGGAGAGGCCTACCTTCGAGTACCTGCAGTCCTTCCTG
GAGGACTACTTCACCTCCGCTGAACCACAGTACCAGCCCGGGGATCAGACATAGCCTGTCCGGG
CATCAACCCTCTCTGGCGGTGGCCACCAGTCCTTGCCAATCCCCAGAGCTGTTCTTCCAAAGCC
CCCAGGCTGGCTTAGAACCCCATAGAGTCCTAGCATCACCGAGGACGTGGCTGCTCTGACACCA
CCTAGGGCAACCTACTTGTTTTACAGATGGGGCAAAAGGAGGCCCAGAGCTGATCTCTCATCCG
CTCTGGCCCCAAGCACTATTTCTTCCTTTTCCACTTAGGCCCCTACATGCCTGTAGCCTTTCTC
ACTCCATCCCCACCCAAAGTGCTCAGACCTTGTCTAGTTATTTATAAAACTGTATGTACCTCCC
TCACTTCTCTCCTATCACTGCTTTCCTACTCTCCTTTTATCTCACTCTAGTCCAGGTGCCAAGA
ATTTCCCTTCTACCCTCTATTCTCTTGTGTCTGTAAGTTACAAAGTCAGGAAAAGTCTTGGCTG
GACCCCTTTCCTGCTGGGTGGATGCAGTGGTCCAGGACTGGGGTCTGGGCCCAGGTTTGAGGGA
GAAGGTTGCAGAGCACTTCCCACCTCTCTGAATAGTGTGTATGTGTTGGTTTATTGATTCTGTA
AATAAGTAAAATGACAATATGAATCCTCAAACCATGAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001036194	(Get FASTA)	NCBI Sequence Viewer
	NP_001036212	(Get FASTA)	NCBI Sequence Viewer
	NP_005239	(Get FASTA)	NCBI Sequence Viewer
	XP_006710515	(Get FASTA)	NCBI Sequence Viewer
	XP_011539312	(Get FASTA)	NCBI Sequence Viewer
	XP_011539313	(Get FASTA)	NCBI Sequence Viewer
	XP_011539314	(Get FASTA)	NCBI Sequence Viewer
	XP_011539315	(Get FASTA)	NCBI Sequence Viewer
	XP_011539316	(Get FASTA)	NCBI Sequence Viewer
	XP_016856162	(Get FASTA)	NCBI Sequence Viewer
	XP_016856163	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA35679	(Get FASTA)	NCBI Sequence Viewer
	AAA52451	(Get FASTA)	NCBI Sequence Viewer
	AAA52452	(Get FASTA)	NCBI Sequence Viewer
	AAA52762	(Get FASTA)	NCBI Sequence Viewer
	AAA60585	(Get FASTA)	NCBI Sequence Viewer
	AAH64382	(Get FASTA)	NCBI Sequence Viewer
	BAH13403	(Get FASTA)	NCBI Sequence Viewer
	BAH14268	(Get FASTA)	NCBI Sequence Viewer
	CAA36457	(Get FASTA)	NCBI Sequence Viewer
	CAH05603	(Get FASTA)	NCBI Sequence Viewer
	EAX07748	(Get FASTA)	NCBI Sequence Viewer
	EAX07749	(Get FASTA)	NCBI Sequence Viewer
	EAX07750	(Get FASTA)	NCBI Sequence Viewer
	P09769	(Get FASTA)	NCBI Sequence Viewer

Reference Sequences

RefSeq Acc Id:

NP_005239 ⟸ NM_005248

- UniProtKB:

P09769 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI
PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG
DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW
EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ
LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLR
AANILVGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILL
TELITKGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFL
EDYFTSAEPQYQPGDQT

hide sequence

RefSeq Acc Id:

NP_001036194 ⟸ NM_001042729

- UniProtKB:

P09769 (UniProtKB/Swiss-Prot), P78453 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI
PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG
DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW
EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ
LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLR
AANILVGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILL
TELITKGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFL
EDYFTSAEPQYQPGDQT

hide sequence

RefSeq Acc Id:

NP_001036212 ⟸ NM_001042747

- UniProtKB:

P09769 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI
PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG
DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW
EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ
LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLR
AANILVGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILL
TELITKGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFL
EDYFTSAEPQYQPGDQT

hide sequence

RefSeq Acc Id:	XP_006710515 ⟸ XM_006710452
- Peptide Label:	isoform X1
- UniProtKB:	P09769 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLR AANILVGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILL TELITKGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFL EDYFTSAEPQYQPGDQT hide sequence

RefSeq Acc Id:	XP_011539312 ⟸ XM_011541010
- Peptide Label:	isoform X1
- UniProtKB:	P09769 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLR AANILVGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILL TELITKGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFL EDYFTSAEPQYQPGDQT hide sequence

RefSeq Acc Id:

XP_011539314 ⟸ XM_011541012

- Peptide Label:

isoform X3

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI
PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG
DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW
EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ
LYAVVSEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVPSSPSSGQPQKLPSLADS
PSSQTCGPLGSCSLSSSPRAESPTQA

hide sequence

RefSeq Acc Id:

XP_011539313 ⟸ XM_011541011

- Peptide Label:

isoform X2

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSVKVTGGRLGLSAPEKLAAFPATTWPLLTQSKLKSAYSLSIRDWDQTRGDHVKH
YKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAWEISRS
SITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQLYAVV
SEEPIYIVTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLRAANIL
VGERLACKIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILLTELIT
KGRIPYPGMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFLEDYFT
SAEPQYQPGDQT

hide sequence

RefSeq Acc Id:

XP_011539316 ⟸ XM_011541014

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAWEISRSSITLERR
LGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQLYAVVSEEPIYI
VTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLRAANILVGERLAC
KIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILLTELITKGRIPYP
GMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFLEDYFTSAEPQYQ
PGDQT

hide sequence

RefSeq Acc Id:

XP_011539315 ⟸ XM_011541013

- Peptide Label:

isoform X4

- Sequence:

show sequence

MGCVFCKKLEPVATAKEDAGLEGDFRSYGAADHYGPDPTKARPASSFAHIPNYSNFSSQAINPG
FLDSGTIRGVSGIGVTLFIALYDYEARTEDDLTFTKGEKFHILNNTEGDWWEARSLSSGKTGCI
PSNYVAPVDSIQAEEWYFGKIGRKDAERQLLSPGNPQGAFLIRESETTKGAYSLSIRDWDQTRG
DHVKHYKIRKLDMGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAW
EISRSSITLERRLGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQ
LYAVVSEEPIYIVTEFMCHACWIFSRTQRARI

hide sequence

RefSeq Acc Id:

XP_016856163 ⟸ XM_017000674

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAWEISRSSITLERR
LGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQLYAVVSEEPIYI
VTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLRAANILVGERLAC
KIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILLTELITKGRIPYP
GMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFLEDYFTSAEPQYQ
PGDQT

hide sequence

RefSeq Acc Id:

XP_016856162 ⟸ XM_017000673

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGGYYITTRVQFNSVQELVQHYMEVNDGLCNLLIAPCTIMKPQTLGLAKDAWEISRSSITLERR
LGTGCFGDVWLGTWNGSTKVAVKTLKPGTMSPKAFLEEAQVMKLLRHDKLVQLYAVVSEEPIYI
VTEFMCHGSLLDFLKNPEGQDLRLPQLVDMAAQVAEGMAYMERMNYIHRDLRAANILVGERLAC
KIADFGLARLIKDDEYNPCQGSKFPIKWTAPEAALFGRFTIKSDVWSFGILLTELITKGRIPYP
GMNKREVLEQVEQGYHMPCPPGCPASLYEAMEQTWRLDPEERPTFEYLQSFLEDYFTSAEPQYQ
PGDQT

hide sequence

RefSeq Acc Id:

ENSP00000382126 ⟸ ENST00000399173

RefSeq Acc Id:

ENSP00000363116 ⟸ ENST00000374004

RefSeq Acc Id:

ENSP00000363117 ⟸ ENST00000374005

RefSeq Acc Id:

ENSP00000363115 ⟸ ENST00000374003

RefSeq Acc Id:

ENSP00000407670 ⟸ ENST00000457296

Protein Domains

Protein kinase SH2 SH3

Promoters

RGD ID:

6854688

Promoter ID:

EPDNEW_H509

Type:

initiation region

Name:

FGR_1

Description:

FGR proto-oncogene, Src family tyrosine kinase

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	27,635,143 - 27,635,203	EPDNEW

RGD ID:

6785582

Promoter ID:

HG_KWN:1583

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

UC001BOI.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,814,266 - 27,815,217 (-)	MPROMDB

RGD ID:

6785583

Promoter ID:

HG_KWN:1584

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

UC001BOJ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,822,661 - 27,823,957 (-)	MPROMDB

RGD ID:

6809548

Promoter ID:

HG_ACW:1229

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

FGR.GAPR07, FGR.KAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,824,316 - 27,824,816 (-)	MPROMDB

RGD ID:

6785584

Promoter ID:

HG_KWN:1585

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

NM_001042729, NM_001042747, OTTHUMT00000009774, OTTHUMT00000009777, OTTHUMT00000009778

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,825,341 - 27,826,467 (-)	MPROMDB

RGD ID:

6814445

Promoter ID:

HG_XEF:130

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

NM_001098991

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,829,866 - 27,830,366 (-)	MPROMDB

RGD ID:

6809550

Promoter ID:

HG_ACW:1231

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid, NB4

Transcripts:

FGR.HAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,833,299 - 27,833,799 (-)	MPROMDB

RGD ID:

6785585

Promoter ID:

HG_KWN:1586

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

OTTHUMT00000009772, OTTHUMT00000009776

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,833,961 - 27,834,461 (-)	MPROMDB

RGD ID:

6851426

Promoter ID:

EP73513

Type:

initiation region

Name:

HS_FGR

Description:

Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	27,834,242 - 27,834,302	EPD

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1p36.11-35.2(chr1:26963045-32279045)x3	copy number gain	See cases [RCV000051801]	Chr1:26963045..32279045 [GRCh38] Chr1:27289536..32744646 [GRCh37] Chr1:27162123..32517233 [NCBI36] Chr1:1p36.11-35.2	pathogenic
GRCh38/hg38 1p36.11-35.3(chr1:26807012-27685191)x1	copy number loss	See cases [RCV000053799]	Chr1:26807012..27685191 [GRCh38] Chr1:27133503..28011702 [GRCh37] Chr1:27006090..27884289 [NCBI36] Chr1:1p36.11-35.3	pathogenic
GRCh38/hg38 1p35.3(chr1:27601122-27889441)x1	copy number loss	See cases [RCV000053801]	Chr1:27601122..27889441 [GRCh38] Chr1:27927633..28215952 [GRCh37] Chr1:27800220..28088539 [NCBI36] Chr1:1p35.3	pathogenic
NM_001042729.1(FGR):c.891C>T (p.Thr297=)	single nucleotide variant	Malignant melanoma [RCV000060168]	Chr1:27615561 [GRCh38] Chr1:27942072 [GRCh37] Chr1:27814659 [NCBI36] Chr1:1p35.3	not provided
GRCh38/hg38 1p36.11-35.3(chr1:26854636-27645829)x1	copy number loss	See cases [RCV000137657]	Chr1:26854636..27645829 [GRCh38] Chr1:27181127..27972340 [GRCh37] Chr1:27053714..27844927 [NCBI36] Chr1:1p36.11-35.3	uncertain significance
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3	copy number gain	See cases [RCV000138891]	Chr1:24381206..41401517 [GRCh38] Chr1:24707696..41886350 [GRCh37] Chr1:24580283..41658937 [NCBI36] Chr1:1p36.11-34.2	pathogenic
GRCh38/hg38 1p36.11-35.3(chr1:27429343-27699564)x1	copy number loss	See cases [RCV000139133]	Chr1:27429343..27699564 [GRCh38] Chr1:27755852..28026075 [GRCh37] Chr1:27628439..27898662 [NCBI36] Chr1:1p36.11-35.3	uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3	copy number loss	not provided [RCV000762767]	Chr1:20608823..120546301 [GRCh37] Chr1:1p36.12-12	likely benign
GRCh37/hg19 1p36.11-35.3(chr1:27488298-28138628)x1	copy number loss	See cases [RCV000447976]	Chr1:27488298..28138628 [GRCh37] Chr1:1p36.11-35.3	uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	copy number gain	See cases [RCV000510383]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	copy number gain	See cases [RCV000510926]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3	copy number gain	not provided [RCV000736295]	Chr1:47851..249228449 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3	copy number gain	not provided [RCV000736305]	Chr1:82154..249218992 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3	copy number gain	Global developmental delay [RCV000787285]	Chr1:103343285..103455144 [GRCh37] Chr1:1p36.22-21.1	uncertain significance
NM_005248.3(FGR):c.533-8C>G	single nucleotide variant	not provided [RCV000948535]	Chr1:27617014 [GRCh38] Chr1:27943525 [GRCh37] Chr1:1p35.3	benign
NM_005248.3(FGR):c.366C>T (p.Ser122=)	single nucleotide variant	not provided [RCV000950364]	Chr1:27621621 [GRCh38] Chr1:27948132 [GRCh37] Chr1:1p35.3	benign
NM_005248.3(FGR):c.352C>T (p.Arg118Trp)	single nucleotide variant	not provided [RCV001263546]	Chr1:27621635 [GRCh38] Chr1:27948146 [GRCh37] Chr1:1p35.3	uncertain significance
NM_005248.3(FGR):c.1573C>T (p.Pro525Ser)	single nucleotide variant	not provided [RCV001263547]	Chr1:27612931 [GRCh38] Chr1:27939442 [GRCh37] Chr1:1p35.3	uncertain significance

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:3697	AgrOrtholog
COSMIC	FGR	COSMIC
Ensembl Genes	ENSG00000000938	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein	ENSP00000363115	ENTREZGENE, UniProtKB/Swiss-Prot
	ENSP00000363116	ENTREZGENE, UniProtKB/Swiss-Prot
	ENSP00000363117	ENTREZGENE, UniProtKB/Swiss-Prot
	ENSP00000382126	ENTREZGENE, UniProtKB/Swiss-Prot
	ENSP00000407670	ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000374003	ENTREZGENE, UniProtKB/Swiss-Prot
	ENST00000374004	ENTREZGENE, UniProtKB/Swiss-Prot
	ENST00000374005	ENTREZGENE, UniProtKB/Swiss-Prot
	ENST00000399173	ENTREZGENE, UniProtKB/Swiss-Prot
	ENST00000457296	ENTREZGENE, UniProtKB/TrEMBL
Gene3D-CATH	3.30.505.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000000938	GTEx
HGNC ID	HGNC:3697	ENTREZGENE
Human Proteome Map	FGR	Human Proteome Map
InterPro	Fgr_SH2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Kinase-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Prot_kinase_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Protein_kinase_ATP_BS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Ser-Thr/Tyr_kinase_cat_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH2_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3_domain	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Tyr_kinase_AS	UniProtKB/Swiss-Prot
	Tyr_kinase_cat_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:2268	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	2268	ENTREZGENE
OMIM	164940	OMIM
Pfam	Pkinase_Tyr	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA28135	PharmGKB
PRINTS	SH2DOMAIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3DOMAIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	TYRKINASE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	PROTEIN_KINASE_ATP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PROTEIN_KINASE_DOM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PROTEIN_KINASE_TYR	UniProtKB/Swiss-Prot
	SH2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	SH2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SH3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	TyrKc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF50044	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF55550	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF56112	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	FGR_HUMAN	UniProtKB/Swiss-Prot
	L8E733_HUMAN	UniProtKB/TrEMBL
	P09769	ENTREZGENE
	P78453	ENTREZGENE, UniProtKB/TrEMBL
	P78483_HUMAN	UniProtKB/TrEMBL
	Q5TGY6_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	D3DPL7	UniProtKB/Swiss-Prot
	Q9UIQ3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2014-07-01	FGR	FGR proto-oncogene, Src family tyrosine kinase		feline Gardner-Rasheed sarcoma viral oncogene homolog	Symbol and/or name change	5135510	APPROVED
2013-07-16	FGR	feline Gardner-Rasheed sarcoma viral oncogene homolog		Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog	Symbol and/or name change	5135510	APPROVED
2011-08-16	FGR	Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog	FGR	Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog	Symbol and/or name change	5135510	APPROVED

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

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

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

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

Imported Disease Annotations - CTD

Imported Annotations - PID (archival)