VIPR1 (vasoactive intestinal peptide receptor 1)

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Gene: VIPR1 (vasoactive intestinal peptide receptor 1) Homo sapiens

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Symbol:

VIPR1

Name:

vasoactive intestinal peptide receptor 1

RGD ID:

735637

HGNC Page

HGNC:12694

Description:

Enables peptide hormone binding activity and vasoactive intestinal polypeptide receptor activity. Involved in G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger. Part of receptor complex. Implicated in achalasia. Biomarker of Crohn's disease and ulcerative colitis.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

FLJ41949; HVR1; II; PACAP type II receptor; PACAP-R-2; PACAP-R2; pituitary adenylate cyclase activating polypeptide receptor, type II; pituitary adenylate cyclase-activating polypeptide type II receptor; RDC1; type 1 vasoactive intestinal peptide receptor; V1RG; VAPC1; vasoactive intestinal polypeptide receptor 1; VIP and PACAP receptor 1; VIP receptor, type I; VIP-R-1; VIPR; VIRG; VPAC1; VPAC1 receptor; VPAC1R; VPCAP1R

RGD Orthologs

Alliance Orthologs

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	3	42,489,299 - 42,537,568 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	42,489,299 - 42,537,573 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	42,530,791 - 42,579,060 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	42,519,121 - 42,554,064 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	42,519,120 - 42,554,064	NCBI
Celera	3	42,484,508 - 42,519,469 (+)	NCBI		Celera
Cytogenetic Map	3	p22.1	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI		HuRef
CHM1_1	3	42,481,967 - 42,530,261 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	42,507,314 - 42,555,561 (+)	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

achalasia (IAGP)

congenital muscular dystrophy-dystroglycanopathy type A8 (IAGP)

Crohn's disease (IEP)

Experimental Diabetes Mellitus (ISO)

Experimental Liver Cirrhosis (EXP)

hepatocellular carcinoma (EXP)

ulcerative colitis (IEP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

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

1,2-dichloroethane (ISO)

1,2-dimethylhydrazine (ISO)

1-naphthyl isothiocyanate (ISO)

17beta-estradiol (EXP,ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

2,4-dibromophenyl 2,4,5-tribromophenyl ether (ISO)

3,4-methylenedioxymethamphetamine (ISO)

3-methylcholanthrene (EXP)

4,4'-diaminodiphenylmethane (ISO)

4-nonylphenol (EXP)

4-tert-Octylphenol (EXP)

6-propyl-2-thiouracil (ISO)

8-Br-cAMP (EXP)

9-cis-retinoic acid (EXP)

acetamide (ISO)

afimoxifene (EXP)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

all-trans-retinoic acid (EXP,ISO)

amitrole (ISO)

amphetamine (ISO)

arsane (EXP)

arsenic atom (EXP)

arsenite(3-) (EXP,ISO)

benzo[a]pyrene (EXP)

Benzo[k]fluoranthene (ISO)

bisphenol A (ISO)

cadmium dichloride (EXP)

carbon nanotube (ISO)

chenodeoxycholic acid (EXP)

chloroacetaldehyde (EXP)

chlorpyrifos (ISO)

cidofovir anhydrous (EXP)

copper(II) sulfate (EXP)

cyclophosphamide (ISO)

dextran sulfate (ISO)

Dibutyl phosphate (EXP)

dichlorine (ISO)

dioxygen (EXP)

elemental selenium (EXP)

flutamide (ISO)

folic acid (EXP,ISO)

gallic acid (EXP)

glafenine (ISO)

glycidol (ISO)

GW 4064 (EXP)

lipopolysaccharide (EXP)

methimazole (ISO)

methotrexate (ISO)

methoxychlor (ISO)

mono(2-ethylhexyl) phthalate (ISO)

Muraglitazar (ISO)

N-nitrosodiethylamine (ISO)

N-nitrosodimethylamine (ISO)

nebivolol (EXP)

nickel atom (EXP)

nimesulide (ISO)

orphenadrine (ISO)

ozone (ISO)

p-tert-Amylphenol (EXP)

p-toluidine (ISO)

paracetamol (ISO)

PCB138 (ISO)

perfluorooctane-1-sulfonic acid (ISO)

pirinixic acid (EXP,ISO)

propanal (EXP)

quercetin (EXP)

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

selenium atom (EXP)

silicon dioxide (EXP,ISO)

sodium arsenate (EXP)

sulfadimethoxine (ISO)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

triphenyl phosphate (ISO)

troglitazone (ISO)

tunicamycin (ISO)

valproic acid (EXP)

vinclozolin (ISO)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

adenylate cyclase-activating G protein-coupled receptor signaling pathway (IDA)

adenylate cyclase-modulating G protein-coupled receptor signaling pathway (IBA)

cell surface receptor signaling pathway (IEA)

G protein-coupled receptor signaling pathway (IEA,TAS)

G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger (IDA)

positive regulation of cell population proliferation (TAS)

Cellular Component

membrane (IEA)

plasma membrane (IBA,IDA,IEA,TAS)

receptor complex (IDA)

Molecular Function

G protein-coupled peptide receptor activity (IBA)

G protein-coupled receptor activity (IEA)

peptide hormone binding (IBA,IPI)

pituitary adenylate cyclase-activating polypeptide receptor activity (IDA)

protein binding (IPI)

vasoactive intestinal polypeptide receptor activity (IBA,IDA,IEA,ISO,TAS)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Age-dependent association of idiopathic achalasia with vasoactive intestinal peptide receptor 1 gene.	Paladini F, etal., Neurogastroenterol Motil. 2009 Jun;21(6):597-602. Epub 2009 Feb 27.
3.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
5.	Anti-hyperglycemic, antioxidant and anti-inflammatory effects of VIP and a VPAC1 agonist on streptozotocin-induced diabetic mice.	Yu R, etal., Peptides. 2011 Feb;32(2):216-22. Epub 2010 Dec 1.
6.	Differential expression of vasoactive intestinal peptide receptor 1 expression in inflammatory bowel disease.	Yukawa T, etal., Int J Mol Med. 2007 Aug;20(2):161-7.

Additional References at PubMed

PMID:807467	PMID:7708752	PMID:7818527	PMID:7917790	PMID:8179610	PMID:8389448	PMID:8390245	PMID:8639654	PMID:8886855	PMID:8889548	PMID:9927997	PMID:9928020
PMID:9973484	PMID:10867004	PMID:11027527	PMID:11072126	PMID:11160313	PMID:11812005	PMID:11812772	PMID:11834941	PMID:11859927	PMID:11859928	PMID:11930171	PMID:11981043
PMID:12036966	PMID:12050216	PMID:12094871	PMID:12133828	PMID:12225791	PMID:12429744	PMID:12446722	PMID:12477932	PMID:12690118	PMID:14599709	PMID:14702039	PMID:15171718
PMID:15247290	PMID:15451021	PMID:15452121	PMID:15670850	PMID:15932876	PMID:16037943	PMID:16344560	PMID:16520374	PMID:16552823	PMID:16554109	PMID:16888162	PMID:16888167
PMID:16888206	PMID:16888207	PMID:16934434	PMID:17077178	PMID:17110338	PMID:17651798	PMID:17883247	PMID:17885205	PMID:18000164	PMID:18029348	PMID:18174366	PMID:18240029
PMID:18351280	PMID:18383379	PMID:18577758	PMID:18597186	PMID:18663606	PMID:18668120	PMID:19086053	PMID:19598235	PMID:20014941	PMID:20026142	PMID:20424473	PMID:20691743
PMID:20706588	PMID:20922191	PMID:21711977	PMID:21769421	PMID:21873635	PMID:21896307	PMID:21988832	PMID:22166542	PMID:22291440	PMID:22763881	PMID:23382219	PMID:23597562
PMID:23651810	PMID:23898208	PMID:24671823	PMID:24788249	PMID:25390694	PMID:26712708	PMID:26881970	PMID:27381006	PMID:28514442	PMID:28611215	PMID:29117863	PMID:30407703
PMID:30583864	PMID:30692637	PMID:30810849	PMID:31089161	PMID:31408534	PMID:31560089	PMID:32296183	PMID:32807782	PMID:33961781	PMID:35864952	PMID:35869757	PMID:36430275

Genomics

Comparative Map Data

VIPR1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	42,489,299 - 42,537,568 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	42,489,299 - 42,537,573 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	42,530,791 - 42,579,060 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	42,519,121 - 42,554,064 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	42,519,120 - 42,554,064	NCBI
Celera	3	42,484,508 - 42,519,469 (+)	NCBI		Celera
Cytogenetic Map	3	p22.1	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI		HuRef
CHM1_1	3	42,481,967 - 42,530,261 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	42,507,314 - 42,555,561 (+)	NCBI		T2T-CHM13v2.0

Vipr1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	121,471,782 - 121,502,020 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	121,471,782 - 121,502,020 (+)	Ensembl		GRCm39 Ensembl
GRCm38	9	121,642,716 - 121,672,954 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	121,642,716 - 121,672,954 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	121,551,834 - 121,582,072 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	121,491,414 - 121,519,332 (+)	NCBI		MGSCv36	mm8
Celera	9	122,116,040 - 122,146,512 (+)	NCBI		Celera
Cytogenetic Map	9	F4	NCBI
cM Map	9	72.5	NCBI

Vipr1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	130,181,219 - 130,217,098 (+)	NCBI		GRCr8
mRatBN7.2	8	121,303,739 - 121,339,587 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	121,310,248 - 121,339,585 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	126,909,204 - 126,938,516 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	125,108,275 - 125,137,587 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	122,937,779 - 122,967,104 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	130,283,453 - 130,313,431 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_5.0	8	129,467,937 - 129,496,866 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Celera	8	120,444,918 - 120,474,479 (+)	NCBI		Celera
Cytogenetic Map	8	q32	NCBI

Vipr1
(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_004955420	28,234,153 - 28,253,168 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955420	28,234,590 - 28,253,146 (-)	NCBI	ChiLan1.0	ChiLan1.0

VIPR1
(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	2	42,464,670 - 42,503,777 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	3	42,469,438 - 42,504,483 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	3	42,407,591 - 42,442,565 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	3	42,669,338 - 42,705,170 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	3	42,670,195 - 42,705,170 (+)	Ensembl	panpan1.1		panPan2

VIPR1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	23	11,635,809 - 11,666,926 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	23	11,635,394 - 11,666,936 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	23	11,609,898 - 11,641,322 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	23	11,924,939 - 11,956,370 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	23	11,924,529 - 11,957,534 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	23	11,726,543 - 11,757,961 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	23	11,868,801 - 11,900,208 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	23	11,873,062 - 11,904,503 (+)	NCBI		UU_Cfam_GSD_1.0

Vipr1
(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_024405118	200,208,554 - 200,255,619 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936695	2,564,890 - 2,607,676 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936695	2,564,917 - 2,597,009 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

VIPR1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	13	26,036,629 - 26,075,691 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	26,036,610 - 26,073,168 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	13	28,704,211 - 28,740,358 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

VIPR1
(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	22	3,950,129 - 3,984,849 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	22	3,950,193 - 3,984,948 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	163,214,473 - 163,249,573 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Vipr1
(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_004624730	77,128,649 - 77,153,750 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624730	77,128,547 - 77,155,531 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in VIPR1
41 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3p22.1(chr3:41880503-42550279)x3	copy number gain	See cases [RCV000051465]	Chr3:41880503..42550279 [GRCh38] Chr3:41921995..42591771 [GRCh37] Chr3:41896999..42566775 [NCBI36] Chr3:3p22.1	uncertain significance
NM_001251882.1(VIPR1):c.632G>A (p.Arg211Gln)	single nucleotide variant	Malignant melanoma [RCV000066067]	Chr3:42530897 [GRCh38] Chr3:42572389 [GRCh37] Chr3:42547393 [NCBI36] Chr3:3p22.1	not provided
NM_001251882.1(VIPR1):c.633G>A (p.Arg211=)	single nucleotide variant	Malignant melanoma [RCV000066068]	Chr3:42530898 [GRCh38] Chr3:42572390 [GRCh37] Chr3:42547394 [NCBI36] Chr3:3p22.1	not provided
NM_001251882.1(VIPR1):c.646G>A (p.Gly216Arg)	single nucleotide variant	Malignant melanoma [RCV000060824]	Chr3:42530911 [GRCh38] Chr3:42572403 [GRCh37] Chr3:42547407 [NCBI36] Chr3:3p22.1	not provided
GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	copy number gain	See cases [RCV000240519]	Chr3:37028313..49929220 [GRCh37] Chr3:3p22.2-21.31	likely pathogenic
GRCh37/hg19 3p22.1-21.31(chr3:41104508-44636698)x1	copy number loss	See cases [RCV000240302]	Chr3:41104508..44636698 [GRCh37] Chr3:3p22.1-21.31	pathogenic
NM_004624.4(VIPR1):c.571G>A (p.Ala191Thr)	single nucleotide variant	not specified [RCV004331068]	Chr3:42528058 [GRCh38] Chr3:42569550 [GRCh37] Chr3:3p22.1	uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	copy number gain	See cases [RCV000512358]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	copy number gain	See cases [RCV000511055]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	copy number gain	not provided [RCV000682249]	Chr3:16923595..45249923 [GRCh37] Chr3:3p24.3-21.31	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3	copy number gain	not provided [RCV000742138]	Chr3:61495..197838262 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3	copy number gain	not provided [RCV000742133]	Chr3:60174..197948027 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p22.1(chr3:42578509-42723605)x3	copy number gain	not provided [RCV000742385]	Chr3:42578509..42723605 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.1083G>A (p.Pro361=)	single nucleotide variant	not provided [RCV000895984]	Chr3:42535047 [GRCh38] Chr3:42576539 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.614C>T (p.Ser205Leu)	single nucleotide variant	not provided [RCV000946725]	Chr3:42528101 [GRCh38] Chr3:42569593 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.450C>T (p.Tyr150=)	single nucleotide variant	not provided [RCV000882368]	Chr3:42527443 [GRCh38] Chr3:42568935 [GRCh37] Chr3:3p22.1	likely benign
NM_004624.4(VIPR1):c.266T>C (p.Ile89Thr)	single nucleotide variant	not provided [RCV000943752]	Chr3:42519304 [GRCh38] Chr3:42560796 [GRCh37] Chr3:3p22.1	likely benign
NM_004624.4(VIPR1):c.1334G>T (p.Arg445Leu)	single nucleotide variant	not provided [RCV000970296]	Chr3:42536241 [GRCh38] Chr3:42577733 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.1182+9C>T	single nucleotide variant	not provided [RCV000915121]	Chr3:42535393 [GRCh38] Chr3:42576885 [GRCh37] Chr3:3p22.1	likely benign
NM_004624.4(VIPR1):c.377A>G (p.Asp126Gly)	single nucleotide variant	not provided [RCV000906822]	Chr3:42525971 [GRCh38] Chr3:42567463 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.477C>T (p.Val159=)	single nucleotide variant	not provided [RCV000908776]	Chr3:42527470 [GRCh38] Chr3:42568962 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.387G>A (p.Ala129=)	single nucleotide variant	not provided [RCV000970089]	Chr3:42525981 [GRCh38] Chr3:42567473 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.333G>A (p.Thr111=)	single nucleotide variant	not provided [RCV000946724]	Chr3:42525927 [GRCh38] Chr3:42567419 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.400-9C>T	single nucleotide variant	not provided [RCV000916841]	Chr3:42527384 [GRCh38] Chr3:42568876 [GRCh37] Chr3:3p22.1	likely benign
NM_004624.4(VIPR1):c.295C>A (p.Arg99Ser)	single nucleotide variant	not provided [RCV000967740]	Chr3:42525889 [GRCh38] Chr3:42567381 [GRCh37] Chr3:3p22.1	likely benign
NM_004624.4(VIPR1):c.1194G>A (p.Glu398=)	single nucleotide variant	not provided [RCV000894315]	Chr3:42536101 [GRCh38] Chr3:42577593 [GRCh37] Chr3:3p22.1	benign
NM_004624.4(VIPR1):c.89C>T (p.Ala30Val)	single nucleotide variant	not specified [RCV004309921]	Chr3:42513759 [GRCh38] Chr3:42555251 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1365C>T (p.Ser455=)	single nucleotide variant	not provided [RCV000911632]	Chr3:42536272 [GRCh38] Chr3:42577764 [GRCh37] Chr3:3p22.1	likely benign
GRCh37/hg19 3p22.1(chr3:42008472-42610176)x3	copy number gain	not provided [RCV001259688]	Chr3:42008472..42610176 [GRCh37] Chr3:3p22.1	uncertain significance
GRCh37/hg19 3p22.1(chr3:42566141-42673896)	copy number loss	not specified [RCV002053345]	Chr3:42566141..42673896 [GRCh37] Chr3:3p22.1	uncertain significance
NC_000003.11:g.(?_40924962)_(43760024_?)dup	duplication	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8 [RCV001979130]	Chr3:40924962..43760024 [GRCh37] Chr3:3p22.1-21.33	uncertain significance
NM_004624.4(VIPR1):c.784G>T (p.Gly262Cys)	single nucleotide variant	not specified [RCV004113781]	Chr3:42530926 [GRCh38] Chr3:42572418 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1316G>A (p.Arg439His)	single nucleotide variant	not specified [RCV004149530]	Chr3:42536223 [GRCh38] Chr3:42577715 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.130G>A (p.Glu44Lys)	single nucleotide variant	not specified [RCV004071426]	Chr3:42513800 [GRCh38] Chr3:42555292 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.224C>A (p.Ala75Asp)	single nucleotide variant	not specified [RCV004160624]	Chr3:42519262 [GRCh38] Chr3:42560754 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1030C>A (p.Leu344Ile)	single nucleotide variant	not specified [RCV004149185]	Chr3:42534994 [GRCh38] Chr3:42576486 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.406A>T (p.Thr136Ser)	single nucleotide variant	not specified [RCV004114334]	Chr3:42527399 [GRCh38] Chr3:42568891 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.161C>A (p.Ala54Asp)	single nucleotide variant	not specified [RCV004077697]	Chr3:42513831 [GRCh38] Chr3:42555323 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.844G>A (p.Asp282Asn)	single nucleotide variant	not specified [RCV004266624]	Chr3:42531524 [GRCh38] Chr3:42573016 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1082C>T (p.Pro361Leu)	single nucleotide variant	not specified [RCV004339151]	Chr3:42535046 [GRCh38] Chr3:42576538 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1067T>C (p.Met356Thr)	single nucleotide variant	not specified [RCV004356158]	Chr3:42535031 [GRCh38] Chr3:42576523 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.5G>A (p.Arg2His)	single nucleotide variant	not specified [RCV004345489]	Chr3:42502740 [GRCh38] Chr3:42544232 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.820A>T (p.Thr274Ser)	single nucleotide variant	not specified [RCV004482482]	Chr3:42531500 [GRCh38] Chr3:42572992 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.850G>A (p.Gly284Arg)	single nucleotide variant	not specified [RCV004482484]	Chr3:42531530 [GRCh38] Chr3:42573022 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.893A>G (p.Lys298Arg)	single nucleotide variant	not specified [RCV004482485]	Chr3:42531844 [GRCh38] Chr3:42573336 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1109T>C (p.Met370Thr)	single nucleotide variant	not specified [RCV004482474]	Chr3:42535073 [GRCh38] Chr3:42576565 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1190C>A (p.Ala397Glu)	single nucleotide variant	not specified [RCV004482476]	Chr3:42536097 [GRCh38] Chr3:42577589 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.233G>A (p.Arg78Gln)	single nucleotide variant	not specified [RCV004482477]	Chr3:42519271 [GRCh38] Chr3:42560763 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.260C>G (p.Pro87Arg)	single nucleotide variant	not specified [RCV004482478]	Chr3:42519298 [GRCh38] Chr3:42560790 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.433G>A (p.Gly145Ser)	single nucleotide variant	not specified [RCV004482479]	Chr3:42527426 [GRCh38] Chr3:42568918 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.53C>T (p.Ala18Val)	single nucleotide variant	not specified [RCV004482480]	Chr3:42502788 [GRCh38] Chr3:42544280 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.644G>A (p.Cys215Tyr)	single nucleotide variant	not specified [RCV004482481]	Chr3:42530786 [GRCh38] Chr3:42572278 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.821C>G (p.Thr274Ser)	single nucleotide variant	not specified [RCV004482483]	Chr3:42531501 [GRCh38] Chr3:42572993 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.754C>T (p.Arg252Trp)	single nucleotide variant	not specified [RCV004681050]	Chr3:42530896 [GRCh38] Chr3:42572388 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.1072G>A (p.Ala358Thr)	single nucleotide variant	not specified [RCV004681051]	Chr3:42535036 [GRCh38] Chr3:42576528 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.826G>T (p.Ala276Ser)	single nucleotide variant	not specified [RCV004681052]	Chr3:42531506 [GRCh38] Chr3:42572998 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.350C>T (p.Pro117Leu)	single nucleotide variant	not specified [RCV004681049]	Chr3:42525944 [GRCh38] Chr3:42567436 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.418G>C (p.Gly140Arg)	single nucleotide variant	not specified [RCV004681053]	Chr3:42527411 [GRCh38] Chr3:42568903 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.635C>T (p.Ser212Leu)	single nucleotide variant	not specified [RCV004681055]	Chr3:42528122 [GRCh38] Chr3:42569614 [GRCh37] Chr3:3p22.1	uncertain significance
NM_004624.4(VIPR1):c.55C>G (p.Leu19Val)	single nucleotide variant	not specified [RCV004681056]	Chr3:42502790 [GRCh38] Chr3:42544282 [GRCh37] Chr3:3p22.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	7279
Count of miRNA genes:	1159
Interacting mature miRNAs:	1502
Transcripts:	ENST00000325123, ENST00000433647, ENST00000436487, ENST00000438259, ENST00000439731, ENST00000439910, ENST00000443646, ENST00000446673, ENST00000450274, ENST00000465338, ENST00000473495, ENST00000473575, ENST00000487545, ENST00000490161, ENST00000495189, ENST00000498102, ENST00000543411
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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
407367191	GWAS1016167_H	blood protein measurement QTL GWAS1016167 (human)		1e-50	blood protein measurement	blood protein measurement (CMO:0000028)	3	42533316	42533317	Human
1298487	BFD1_H	Body fluid distribution QTL 1 (human)	3.94		Body fluid distribution	impedance ratio	3	36380712	62380712	Human
407365298	GWAS1014274_H	blood protein measurement QTL GWAS1014274 (human)		1e-53	blood protein measurement	blood protein measurement (CMO:0000028)	3	42533316	42533317	Human
407160563	GWAS809539_H	cerebrospinal fluid clusterin measurement QTL GWAS809539 (human)		0.000003	cerebrospinal fluid clusterin measurement		3	42530054	42530055	Human
407365296	GWAS1014272_H	blood protein measurement QTL GWAS1014272 (human)		9e-67	blood protein measurement	blood protein measurement (CMO:0000028)	3	42533316	42533317	Human
1298489	RA4_H	Rheumatoid arthritis QTL 4 (human)		0.0283	Joint/bone inflammation	rheumatoid arthritis	3	36380712	62380712	Human
1643509	BW293_H	Body Weight QTL 293 (human)	1.42		Body weight	BMI	3	36380712	62380712	Human
407417509	GWAS1066485_H	nucleotide measurement QTL GWAS1066485 (human)		0.000003	nucleotide metabolism trait (VT:0003806)		3	42531930	42531931	Human
407367194	GWAS1016170_H	blood protein measurement QTL GWAS1016170 (human)		3e-59	blood protein measurement	blood protein measurement (CMO:0000028)	3	42533316	42533317	Human
2316061	GLUCO194_H	Glucose level QTL 194 (human)		0.02	Glucose level		3	23380774	49380774	Human
2289308	BW392_H	Body weight QTL 392 (human)	1.42		Body weight	BMI	3	36380712	62380712	Human
407298617	GWAS947593_H	BMI-adjusted hip circumference QTL GWAS947593 (human)		0.000008	BMI-adjusted hip circumference	hip circumference (CMO:0000014)	3	42523132	42523133	Human

Markers in Region

SHGC-85073

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,556,410 - 42,556,680	UniSTS	GRCh37
Build 36	3	42,531,414 - 42,531,684	RGD	NCBI36
Celera	3	42,496,814 - 42,497,084	RGD
Cytogenetic Map	3	p22	UniSTS
HuRef	3	42,600,524 - 42,600,794	UniSTS
TNG Radiation Hybrid Map	3	25957.0	UniSTS

G59451

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,571,450 - 42,571,643	UniSTS	GRCh37
Build 36	3	42,546,454 - 42,546,647	RGD	NCBI36
Celera	3	42,511,854 - 42,512,048	RGD
Cytogenetic Map	3	p22	UniSTS
HuRef	3	42,615,563 - 42,615,757	UniSTS
TNG Radiation Hybrid Map	3	26006.0	UniSTS

D3S1497

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,565,072 - 42,565,188	UniSTS	GRCh37
Build 36	3	42,540,076 - 42,540,192	RGD	NCBI36
Celera	3	42,505,476 - 42,505,592	RGD
Cytogenetic Map	3	p22	UniSTS
HuRef	3	42,609,185 - 42,609,301	UniSTS

VIPR1_387

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,578,345 - 42,579,229	UniSTS	GRCh37
Build 36	3	42,553,349 - 42,554,233	RGD	NCBI36
Celera	3	42,518,749 - 42,519,633	RGD
HuRef	3	42,622,460 - 42,623,344	UniSTS

RH68684

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,578,927 - 42,579,025	UniSTS	GRCh37
Build 36	3	42,553,931 - 42,554,029	RGD	NCBI36
Celera	3	42,519,331 - 42,519,429	RGD
Cytogenetic Map	3	p22	UniSTS
HuRef	3	42,623,042 - 42,623,140	UniSTS
GeneMap99-GB4 RH Map	3	139.81	UniSTS
NCBI RH Map	3	382.4	UniSTS

SHGC-76862

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	42,578,208 - 42,578,536	UniSTS	GRCh37
Build 36	3	42,553,212 - 42,553,540	RGD	NCBI36
Celera	3	42,518,612 - 42,518,940	RGD
Cytogenetic Map	3	p22	UniSTS
HuRef	3	42,622,323 - 42,622,651	UniSTS
TNG Radiation Hybrid Map	3	26010.0	UniSTS
GeneMap99-GB4 RH Map	3	143.16	UniSTS
Whitehead-RH Map	3	171.2	UniSTS
Whitehead-YAC Contig Map	3		UniSTS

MARC_17029-17030:1023294211:1

Human Assembly	Chr	Position (strand)	Source	JBrowse
HuRef	3	42,613,031 - 42,613,696	UniSTS

GDB:455353

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	3	p22	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2430	2788	2239	4903	1715	2309	6	618	1720	459	2221	7041	6248	42	3708	1	821	1728	1581	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_030371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001251882	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001251883	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001251884	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001251885	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_004624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005265437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005265438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005265439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448850	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448851	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347746	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347748	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001740254	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001740255	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007095725	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486791	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486792	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_940500	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB065669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC092047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH005329	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ012074	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK123943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK126759	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293548	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294609	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK314334	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY077579	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC064424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU681817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA200439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF577396	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FB659868	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L13288	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L20295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X75299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000325123 ⟹ ENSP00000327246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,643 - 42,537,568 (+)	Ensembl

Ensembl Acc Id:

ENST00000433647 ⟹ ENSP00000394950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,489,299 - 42,537,567 (+)	Ensembl

Ensembl Acc Id:

ENST00000436487 ⟹ ENSP00000393215

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,612 - 42,532,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000438259 ⟹ ENSP00000415371

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,612 - 42,537,573 (+)	Ensembl

Ensembl Acc Id:

ENST00000439731 ⟹ ENSP00000403478

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,623 - 42,530,932 (+)	Ensembl

Ensembl Acc Id:

ENST00000439910 ⟹ ENSP00000403680

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,617 - 42,536,544 (+)	Ensembl

Ensembl Acc Id:

ENST00000443646 ⟹ ENSP00000388479

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,612 - 42,536,394 (+)	Ensembl

Ensembl Acc Id:

ENST00000446673 ⟹ ENSP00000396204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,664 - 42,532,333 (+)	Ensembl

Ensembl Acc Id:

ENST00000450274 ⟹ ENSP00000415013

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,501,912 - 42,527,496 (+)	Ensembl

Ensembl Acc Id:

ENST00000465338

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,529,734 - 42,531,526 (+)	Ensembl

Ensembl Acc Id:

ENST00000473495

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,489,480 - 42,500,416 (+)	Ensembl

Ensembl Acc Id:

ENST00000473575

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,513,799 - 42,527,899 (+)	Ensembl

Ensembl Acc Id:

ENST00000487545

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,489,494 - 42,519,314 (+)	Ensembl

Ensembl Acc Id:

ENST00000490161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,489,483 - 42,500,146 (+)	Ensembl

Ensembl Acc Id:

ENST00000495189

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,527,653 - 42,530,897 (+)	Ensembl

Ensembl Acc Id:

ENST00000498102

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,532,866 - 42,537,567 (+)	Ensembl

Ensembl Acc Id:

ENST00000543411 ⟹ ENSP00000445701

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	42,502,612 - 42,537,573 (+)	Ensembl

RefSeq Acc Id:

NM_001251882 ⟹ NP_001238811

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,489,299 - 42,537,568 (+)	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI
CHM1_1	3	42,481,967 - 42,530,261 (+)	NCBI
T2T-CHM13v2.0	3	42,507,314 - 42,555,561 (+)	NCBI

Sequence:

show sequence

ATTTTCCCAGCTTACTAGTGGAAAAGCAGCTTCTTTCCCACAGTTCCAGCAAAAGCCCCAGGGC
TGATGCTCATTGGCCCAGGTTGGGGCATGTGACCATTGGCAAGACTCCCATTGGCCAGGCCTGG
GGCAGGTGCTCACTACTGGAGCCAGAGCGGAGTATAAGCCCTACCCAATCACTGAACTACGTGG
GTCAAGAGTAAAGGAGCTGTGGCTTCCCCCCAATCAGAAGGGCACTGGATGATGGATGAACTCT
GTGTGGTGCGTCTTCACACTGACACCAGGAGGATAAGGAAGTGACTCCCTCAGCTGAGTGGCTG
GCATGTGCCAGGCTAGAGCAGCTTGGCTATGGCAGAACATCCAGCCCCACCGTGTGGACGGCAG
AGATGAGGAAACTGGTGTGGGGTTGCCGGGGCCAGCAACCACTTTTCTAAAGCCAAAGACGCAG
AAGGTGCTGCCAGTCCAACGCTTCCTCCATGGAGGCCTTCACCCACCCACACCCATCTAAGAGT
TCCCAAGACCTGTTTTTTCTGGCTATTCCTAGACAGCCATCACCCCCACTCACATGTCTTCCAC
AAGGGCGGCCAGGCGGCCAGGCTGCAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGC
ACAAGCAGTGCCTGGAGGAGGCCCAGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGA
CAACCTCACCTGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATC
TTCAAGCTCTTCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGA
CGCACCTGGAGCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGA
TGAGCAGCAGACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCC
CTCGCCACCCTTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGA
ACTACATCCACATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGA
CTTGGCCCTCTTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCA
GCCATGGTCTTTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCT
ACCTGTACACCCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACT
CATCGGCTGGGGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAG
GATTATGGGTGCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCA
CCTCCATCTTGGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCG
GCCCCCAGATATCAGGAAGAGTGACAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTG
CTGATCCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTG
AAGTGAAGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTA
CTGCTTCCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAG
GGCGTCCTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCA
GCACGCAGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGC
CGAAGTCTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCC
CACTCACCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGC
TCGGAGGCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAG
CCTGCCTGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTG
GAACTCAGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACA
TACTTTCATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGG
ATCCTCAAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCAC
CAACACCACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACC
ACTCAGGCATTTGACTGAAGATGCAGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGC
TTTTTAAAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCAC
CGAAGTGGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACT
CTGAAGCCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACC
TGCTCTCCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCT
CTCTGTGCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAA
CTGTTGTAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCT
GCTACACATACAGGATTTGAACTCAGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACT
GCTAACTTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATT
AATGCCATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCT
CCATCTCATGTATCATCTGGATAGGAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCC
CAGTGGCCACTCAGCTTCCTACCCACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCT
TGTGCAACAATAAATGTTGGCTTGGA

hide sequence

RefSeq Acc Id:

NM_001251883 ⟹ NP_001238812

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI
CHM1_1	3	42,495,280 - 42,530,261 (+)	NCBI
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGCTGCAGCAAGATGTGGGACA
ACCTCACCTGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTT
CAAGCTCTTCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACG
CACCTGGAGCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATG
AGGTGGGCTGTAAGGCAGCCATGGTCTTTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCT
GCTGGTGGAGGGCCTCTACCTGTACACCCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTAC
TTCTGGGGGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGAT
TATGGGTGCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCT
CCATCTTGGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCC
CCCAGATATCAGGAAGAGTGACAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCTG
ATCCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAAG
TGAAGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACTG
CTTCCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGGC
GTCCTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGCA
CGCAGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCGA
AGTCTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCAC
TCACCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTCG
GAGGCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCCT
GCCTGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGAA
CTCAGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATAC
TTTCATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGATC
CTCAAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCAA
CACCACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCACT
CAGGCATTTGACTGAAGATGCAGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTTT
TTAAAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCGA
AGTGGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCTG
AAGCCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTGC
TCTCCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCTC
TGTGCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACTG
TTGTAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGCT
ACACATACAGGATTTGAACTCAGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGCT
AACTTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAAT
GCCATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCCA
TCTCATGTATCATCTGGATAGGAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCAG
TGGCCACTCAGCTTCCTACCCACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTGT
GCAACAATAAATGTTGGCTTGGA

hide sequence

RefSeq Acc Id:

NM_001251884 ⟹ NP_001238813

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI
CHM1_1	3	42,495,280 - 42,530,261 (+)	NCBI
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGCTGCAGCAAGATGTGGGACA
ACCTCACCTGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTT
CAAGCTCTTCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACG
CACCTGGAGCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATG
AGCAGACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGC
CACCCTTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTAC
ATCCACATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGG
CCCTCTTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCAT
GGTCTTTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTG
TACACCCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCATCG
GCTGGGGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGATTA
TGGGTGCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCTCC
ATCTTGGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCCCC
CAGATATCAGGAAGAGTGACAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCTGAT
CCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAAGTG
AAGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACTGCT
TCCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGGCGT
CCTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGCACG
CAGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCGAAG
TCTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCACTC
ACCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTCGGA
GGCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCCTGC
CTGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGAACT
CAGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATACTT
TCATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGATCCT
CAAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCAACA
CCACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCACTCA
GGCATTTGACTGAAGATGCAGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTTTTT
AAAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCGAAG
TGGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCTGAA
GCCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTGCTC
TCCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCTCTG
TGCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACTGTT
GTAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGCTAC
ACATACAGGATTTGAACTCAGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGCTAA
CTTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAATGC
CATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCCATC
TCATGTATCATCTGGATAGGAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCAGTG
GCCACTCAGCTTCCTACCCACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTGTGC
AACAATAAATGTTGGCTTGGA

hide sequence

RefSeq Acc Id:

NM_001251885 ⟹ NP_001238814

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI
CHM1_1	3	42,495,280 - 42,530,261 (+)	NCBI
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCTGCAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGCACAAGC
AGTGCCTGGAGGAGGCCCAGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGACAACCT
CACCTGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTTCAAG
CTCTTCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACGCACC
TGGAGCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATGAGCA
GCAGACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGCC
ACCCTTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTACA
TCCACATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGGC
CCTCTTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCATG
GTCTTTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTGT
ACACCCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCATCGG
CTGGGGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGATTAT
GGGTGCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCTCCA
TCTTGGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCCCCC
AGATATCAGGAAGAGTGACAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCTGATC
CCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAAGTGA
AGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACTGCTT
CCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGGCGTC
CTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGCACGC
AGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCGAAGT
CTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCACTCA
CCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTCGGAG
GCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCCTGCC
TGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGAACTC
AGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATACTTT
CATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGATCCTC
AAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCAACAC
CACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCACTCAG
GCATTTGACTGAAGATGCAGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTTTTTA
AAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCGAAGT
GGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCTGAAG
CCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTGCTCT
CCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCTCTGT
GCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACTGTTG
TAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGCTACA
CATACAGGATTTGAACTCAGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGCTAAC
TTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAATGCC
ATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCCATCT
CATGTATCATCTGGATAGGAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCAGTGG
CCACTCAGCTTCCTACCCACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTGTGCA
ACAATAAATGTTGGCTTGGA

hide sequence

RefSeq Acc Id:

NM_004624 ⟹ NP_004615

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI
Build 36	3	42,519,121 - 42,554,064 (+)	NCBI Archive
HuRef	3	42,574,992 - 42,623,180 (+)	NCBI
CHM1_1	3	42,495,280 - 42,530,261 (+)	NCBI
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGGCGGCCAGGCGGCCAGGCTG
CAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGCACAAGCAGTGCCTGGAGGAGGCCC
AGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGACAACCTCACCTGCTGGCCAGCCAC
CCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTTCAAGCTCTTCTCCTCCATTCAA
GGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACGCACCTGGAGCCTGGCCCGTACC
CCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATGAGCAGCAGACCATGTTCTACGG
TTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGCCACCCTTCTGGTCGCCACA
GCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTACATCCACATGCACCTCTTCA
TATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGGCCCTCTTCGACAGCGGGGA
GTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCATGGTCTTTTTCCAATATTGT
GTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTGTACACCCTGCTTGCCGTCT
CCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCATCGGCTGGGGGGTACCCAGCAC
ATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGATTATGGGTGCTGGGACACCATC
AACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCTCCATCTTGGTAAACTTCATCC
TGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCCCCCAGATATCAGGAAGAGTGA
CAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCTGATCCCCCTGTTTGGAGTACAC
TACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAAGTGAAGATGGTCTTTGAGCTCG
TCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACTGCTTCCTCAATGGTGAGGTGCA
GGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGGCGTCCTGGGCTGGAACCCCAAA
TACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGCACGCAGGTTTCCATGCTGACCC
GCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCGAAGTCTCCCTGGTCTGACCACC
AGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCACTCACCCCGGCAGACGCCGGGG
ACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTCGGAGGCTGCCCCCGGCCCCCTG
GTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCCTGCCTGGAGCGTTTCTAGCAAG
TGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGAACTCAGTCATTAGACTCCTCCT
CCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATACTTTCATCCTGACTCTGCCCCC
TGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGATCCTCAAACAACACTGGTGTGAC
CTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCAACACCACGGTAGTGCCTGAAAT
TTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCACTCAGGCATTTGACTGAAGATGC
AGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTTTTTAAAGTGGGTTATTCTGGAG
TTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCGAAGTGGACTGGCCCCTGGGTCA
GTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCTGAAGCCTCTGGGAAATGAGAAG
GCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTGCTCTCCAAGTCTCAGTGGCTTC
ATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCTCTGTGCTGTGGAAGCAACAGGA
ATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACTGTTGTAACTAGGCTCAGAGATG
TGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGCTACACATACAGGATTTGAACTC
AGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGCTAACTTTTGTGTATCGTAACCA
GCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAATGCCATTATCCCTGAATCCCCC
TTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCCATCTCATGTATCATCTGGATAG
GAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCAGTGGCCACTCAGCTTCCTACCC
ACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTGTGCAACAATAAATGTTGGCTTG
GA

hide sequence

RefSeq Acc Id:

XM_005265437 ⟹ XP_005265494

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGGCGGCCAGGCGGCCAGGCTG
CAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGCACAAGCAGTGCCTGGAGGAGGCCC
AGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGACAACCTCACCTGCTGGCCAGCCAC
CCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTTCAAGCTCTTCTCCTCCATTCAA
GGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACGCACCTGGAGCCTGGCCCGTACC
CCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATGAGCAGACCATGTTCTACGGTTC
TGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGCCACCCTTCTGGTCGCCACAGCT
ATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTACATCCACATGCACCTCTTCATAT
CCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGGCCCTCTTCGACAGCGGGGAGTC
GGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCATGGTCTTTTTCCAATATTGTGTC
ATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTGTACACCCTGCTTGCCGTCTCCT
TCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCATCGGCTGGGGGGTACCCAGCACATT
CACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGATTATGGGTGCTGGGACACCATCAAC
TCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCTCCATCTTGGTAAACTTCATCCTGT
TTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCCCCCAGATATCAGGAAGAGTGACAG
CAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCTGATCCCCCTGTTTGGAGTACACTAC
ATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAAGTGAAGATGGTCTTTGAGCTCGTCG
TGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACTGCTTCCTCAATGGTGAGGTGCAGGC
GGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGGCGTCCTGGGCTGGAACCCCAAATAC
CGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGCACGCAGGTTTCCATGCTGACCCGCG
TCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCGAAGTCTCCCTGGTCTGACCACCAGG
ATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCACTCACCCCGGCAGACGCCGGGGACA
GAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTCGGAGGCTGCCCCCGGCCCCCTGGTC
TCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCCTGCCTGGAGCGTTTCTAGCAAGTGA
GAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGAACTCAGTCATTAGACTCCTCCTCCA
AAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATACTTTCATCCTGACTCTGCCCCCTGC
TGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGATCCTCAAACAACACTGGTGTGACCTG
AGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCAACACCACGGTAGTGCCTGAAATTTC
ACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCACTCAGGCATTTGACTGAAGATGCAGC
TCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTTTTTAAAGTGGGTTATTCTGGAGTTT
TTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCGAAGTGGACTGGCCCCTGGGTCAGTC
TGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCTGAAGCCTCTGGGAAATGAGAAGGCA
GCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTGCTCTCCAAGTCTCAGTGGCTTCATC
TGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCTCTGTGCTGTGGAAGCAACAGGAATC
AAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACTGTTGTAACTAGGCTCAGAGATGTGC
ACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGCTACACATACAGGATTTGAACTCAGA
TCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGCTAACTTTTGTGTATCGTAACCAGCC
AGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAATGCCATTATCCCTGAATCCCCCTTG
CCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCCATCTCATGTATCATCTGGATAGGAG
CCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCAGTGGCCACTCAGCTTCCTACCCACA
CCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTGTGCAACAATAAATGTTGGCTTGGAT
TGGC

hide sequence

RefSeq Acc Id:

XM_005265439 ⟹ XP_005265496

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,537,568 (+)	NCBI
GRCh37	3	42,530,791 - 42,579,065 (+)	NCBI

Sequence:

show sequence

ACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCTCTTTGCCCGCGCGG
GGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCCGCTGGCT
ATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGCTGCAGCAAGATGTGGGACA
ACCTCACCTGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTT
CAAGCTCTTCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACG
CACCTGGAGCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATG
AGCAGCAGACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCT
CGCCACCCTTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAAC
TACATCCACATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACT
TGGCCCTCTTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGC
CATGGTCTTTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTAC
CTGTACACCCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCA
TCGGCTGGGGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGA
TTATGGGTGCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACC
TCCATCTTGGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGC
CCCCAGATATCAGGAAGAGTGACAGCAGTCCATACTCAAGGCTAGCCAGGTCCACACTCCTGCT
GATCCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCCGGACAATTTTAAGCCTGAA
GTGAAGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGGGTTTTGTGGTGGCTATCCTCTACT
GCTTCCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAAGTGGCGGCGCTGGCACCTGCAGGG
CGTCCTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGAGGCAGCAACGGCGCCACGTGCAGC
ACGCAGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCCGCCGCTCCTCCAGCTTCCAAGCCG
AAGTCTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAAGGCGGCCCCTCCCGCCCCTTCCCA
CTCACCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGCGCGGCCAGCCCCGGCCCTGGGCTC
GGAGGCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACTCCTAGAGAACGCAGCCCTAGAGCC
TGCCTGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTCCTCTCCTGGAGGATTGCAGGTGGA
ACTCAGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCCAATCAAGGGCAAAAAGTCTACATA
CTTTCATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCAATTGGAGGAAAGCAACCGGTGGAT
CCTCAAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTCTGCCCGGGAAGGTCACCAGCACCA
ACACCACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAGTTCCTTTGGGTTAAGCATTACCAC
TCAGGCATTTGACTGAAGATGCAGCTCACTACCCTATTCTCTCTTTACGCTTAGTTATCAGCTT
TTTAAAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCACACCTATCTTAGTGGTTCCCCACCG
AAGTGGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGTGCAACCCAAGGACTGAGGGACTCT
GAAGCCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGCTAGGTCTCGGACTAAGCCTACCTG
CTCTCCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCTGTCACACCAGCCATACTTATCTCT
CTGTGCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCTTGTCCACCCACCTATGTGCCAACT
GTTGTAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGACAGAAAGCAGATACCTCACCCTGC
TACACATACAGGATTTGAACTCAGATCTGTCTGATAGGAATGTGAAAGCACGGACTCTTACTGC
TAACTTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTATTTGTTTACCACTTGTATTATTAA
TGCCATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCCTGGAGTGTGGCTGAGGAGGCCTCC
ATCTCATGTATCATCTGGATAGGAGCCTGCTGGTCACAGCCTCCTCTGTCTGCCCTTCACCCCA
GTGGCCACTCAGCTTCCTACCCACACCTCTGCCAGAAGATCCCCTCAGGACTGCAACAGGCTTG
TGCAACAATAAATGTTGGCTTGGATTGGC

hide sequence

RefSeq Acc Id:

XM_011534080 ⟹ XP_011532382

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,532,742 (+)	NCBI

Sequence:

show sequence

ACAGCGCCAGCGCCACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCT
CTTTGCCCGCGCGGGGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTG
CCCGCCCGCTGGCTATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGGCGGCC
AGGCGGCCAGGCTGCAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGCACAAGCAGTG
CCTGGAGGAGGCCCAGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGACAACCTCACC
TGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTTCAAGCTCT
TCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACGCACCTGGA
GCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATGAGCAGCAG
ACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGCCACCC
TTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTACATCCA
CATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGGCCCTC
TTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCATGGTCT
TTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTGTACAC
CCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGTACTTCTGGGGGTACATACTCATCGGCTGG
GGGGTACCCAGCACATTCACCATGGTGTGGACCATCGCCAGGATCCATTTTGAGGATTATGGGT
GCTGGGACACCATCAACTCCTCACTGTGGTGGATCATAAAGGGCCCCATCCTCACCTCCATCTT
GGTAAACTTCATCCTGTTTATTTGCATCATCCGAATCCTGCTTCAGAAACTGCGGCCCCCAGAT
ATCAGGAAGAGTGACAGCAGTCCATACTCGTATGCATCTGCTGCCAAGCCAGGGAGCTCAAGAG
GACACCGATGACCTGTGTCTTGTTCATACCATGTGCCCAGTCCCTGGCATGTGCCTCACATGGA
AAAAGGGTGCAATAAACACATAGTAGATGAATGCCCTGGGGGAGACCCCAGTCCACCAATGAGA
CAGCCATGTTCGGGACTCAGTATTCCTCAGTAATAATGATGACACCTGCAGTTTACATGCCAGG
CACACGCTAAGGGATTTCCATGCATCATGTCATTTCATCCACACAGTCCCCTGCAAAATTATCT
TTACTTTACAGGGAGGAAATGACATACACTCCCTTCTCCTTGAGGGTTTTGGAGCAGGTCACCA
TGGGCAGGGAGAAGGGGGCACAATGTCCATGGACCAGGGCTTGGAAAGGTGTCAGGACTGTTCC
CCCTGCTTGGGAGGACTGGAGGAAGAGGCAGGTTTTTTTGCGGGAGCAACAAGGCTTGAAGACA
GAGCTAAAGAAACATGAAAAATATGAAAAGGGAGGCTGTGGGAAGGCAAGTAGGGTCTGCATGC
TCACAGATGGGAGTAGGAGATTGAGTATCAGTGCTATTGACACAAGACAAACCTGGGACGTCCC
ACAAGGCCTTCCAGTCCTGGGATTCTTCTTGGCCTGGCTTCTCTTTGGAGAGTCTGTGCTGTGG
TTCTAAGATTCCTGGCTAGAATGTCACAGACTGCTGGATTTAGGATTCTATTCTGGAATCCTGT
GATTCTCCCTGATGAGACTAAGACTCACATTCCTGGTGTGACTGCATTCTCTCCTGCCAGGTGT
GTAGGCGGAGCTTCCCTTCCTGTCTGAGAAGGAAAGGCTGGGGGGGACGGGGGGGGCATCTGCA
GTCTGCTGAGGGGCAGCACATCGGGCCTGTGCACCCTTATCCTCTCCTTTGCCGATGGGACCTT
ATTTCCCCCAACTTACAATGGTTCAAAAGGGCCTGAATCTGAGGCAAACAGAGCTGGCCATGGT
CAGGGCCAGGTCTGTGTGGTGAGACAGAAAGGAAACAGTTGTCAGCAGGCAAAAGGGGTGGGGG
CAGTTGGAGATGAAGCTCCTCAAGGAGAAGCTGTCAGCTCCCACTCTACACCTCCCCATAAGCC
TTTGATTTAAAGAAAGCCTCCATCTGTTAGCCTCCGGTGTGTGGGATAGTTTTGCAGCCGAAGA
GGGGTGGGCATTGCTCAGGATCTTGGCATGGCTGAGAACCAGGTCCAGGAAGGAGTGGGAGGGG
CAAGGCCAGCTCCTCTGCCCCCAGCTTGCTGTGGGACCTCAGGCCTTGGGCTAGACTTCCTTGG
ACTGACTGCTAAGGCAGGAGAGACAGAGTCAGAGACCCTCCCTATCCACACCCCACCTCTCCTA
GCCAGGGAGCAATGGGTTCACACTGCCTGGATCAGCTATGAGGTCAGGTGGCTGGGAGGCCTGA
ACCAGGAAGAGCTCTGGGCCATGGGAGGCGGGTGAGCATTTAGAATGAATGCTGACCCTACTGA
GCACACAAAGCTGTGAAGAAGGAGCTGGTCCTTCAGAGCACGCTGGGAGTATATGCACTGGTGT
GGGGAGGTAGGAGGAGGGGGATGCAACCCCAGAGAAGGTGGCAACTTCTGGAGAAGCAGACACA
GCAGAAAAAACACAGATAGAGGGCGATACTGATTAATTTTGGGTTGTCCCTGGTGATCAGGTAT
GAACTTGGGTCCCCATCACCCTCCCAAGTGGCCCTGGGCATATGTGGTCAGCACCCAGTTAGAA
AGACTTGTTTCCTAGTACGTCTTCTCTCATGGTCTCTCATGGATGCACTATACTTCATAGTACC
CAAAACACTTCCAAGTTCATAGTGGGCCTCTGTTTCTATAATTTGACTATGTCGAGCATACACT
TACTGCATTATACAAATTGGAAAAACTGAGACCAGGAGAGGAGGAACCAGAATCTCTTGTTGCC
TAAGAGATTTTCTACTGCTCTTGATGGCTGAGAGCATCCTCTACTGCAATGATGAGGTAAGCCT
CTCCTAGACCAGGGGGCCCAGGCAACAGAACTCCCAATAGTGGATTTCAGCTAACATGTCCCTG
TTAGCATCATTCTCACTGGCCTCTCCTTTACCTCTTACCCTCTCTCCTCCAGAAGGGTGAGAAT
AGAGGGGGTTTCTTTCTCTCTCATGCTTCCCTCCAGGCCAGGAGGGCTGGGGGCAGAAGGGCAG
AGGCACTGCAGCTGTGGAACAGGAGCAGACAAGGGCATAATATTCAGAGGAACCTACAGTCCAT
CCTCATACTTCCTGGTCATTGTCCCCATCTTCTGTGCCTCCAGCTGCCCCCATGCCACACCCTA
TCATATCCACATGTGTGGACACACATACCCATGGCCTGTCCCTCCCCTGTCTCCAGAAGGCTAG
CCAGGTCCACACTCCTGCTGATCCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTCTTTCC
GGACAATTTTAAGCCTGAAGTG

hide sequence

RefSeq Acc Id:

XM_047448850 ⟹ XP_047304806

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,532,742 (+)	NCBI

RefSeq Acc Id:

XM_047448851 ⟹ XP_047304807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,527,426 - 42,537,568 (+)	NCBI

RefSeq Acc Id:

XM_054347745 ⟹ XP_054203720

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

RefSeq Acc Id:

XM_054347746 ⟹ XP_054203721

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,555,561 (+)	NCBI

RefSeq Acc Id:

XM_054347747 ⟹ XP_054203722

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,553,054 (+)	NCBI

RefSeq Acc Id:

XM_054347748 ⟹ XP_054203723

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,553,054 (+)	NCBI

RefSeq Acc Id:

XM_054347749 ⟹ XP_054203724

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,545,419 - 42,555,561 (+)	NCBI

RefSeq Acc Id:

XR_007095725

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,532,275 (+)	NCBI

RefSeq Acc Id:

XR_008486791

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,550,268 (+)	NCBI

RefSeq Acc Id:

XR_008486792

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	42,520,639 - 42,550,268 (+)	NCBI

RefSeq Acc Id:

XR_940500

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	42,502,643 - 42,532,275 (+)	NCBI

Sequence:

show sequence

ACAGCGCCAGCGCCACTCTGCCAGGCTCCCGGCCATCGCCCGCCTGGTGCGCCGCCCGCCAGCT
CTTTGCCCGCGCGGGGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTG
CCCGCCCGCTGGCTATGCGTGCTGGCAGGCGCCCTCGCCTGGGCCCTTGGGCCGGCGGGCGGCC
AGGCGGCCAGGCTGCAGGAGGAGTGTGACTATGTGCAGATGATCGAGGTGCAGCACAAGCAGTG
CCTGGAGGAGGCCCAGCTGGAGAATGAGACAATAGGCTGCAGCAAGATGTGGGACAACCTCACC
TGCTGGCCAGCCACCCCTCGGGGCCAGGTAGTTGTCTTGGCCTGTCCCCTCATCTTCAAGCTCT
TCTCCTCCATTCAAGGCCGCAATGTAAGCCGCAGCTGCACCGACGAAGGCTGGACGCACCTGGA
GCCTGGCCCGTACCCCATTGCCTGTGGTTTGGATGACAAGGCAGCGAGTTTGGATGAGCAGCAG
ACCATGTTCTACGGTTCTGTGAAGACCGGCTACACCATTGGCTACGGCCTGTCCCTCGCCACCC
TTCTGGTCGCCACAGCTATCCTGAGCCTGTTCAGGAAGCTCCACTGCACGCGGAACTACATCCA
CATGCACCTCTTCATATCCTTCATCCTGAGGGCTGCCGCTGTCTTCATCAAAGACTTGGCCCTC
TTCGACAGCGGGGAGTCGGACCAGTGCTCCGAGGGCTCGGTGGGCTGTAAGGCAGCCATGGTCT
TTTTCCAATATTGTGTCATGGCTAACTTCTTCTGGCTGCTGGTGGAGGGCCTCTACCTGTACAC
CCTGCTTGCCGTCTCCTTCTTCTCTGAGCGGAAGGGTACCCAGCACATTCACCATGGTGTGGAC
CATCGCCAGGATCCATTTTGAGGATTATGGGTGCTGGGACACCATCAACTCCTCACTGTGGTGG
ATCATAAAGGGCCCCATCCTCACCTCCATCTTGGTAAACTTCATCCTGTTTATTTGCATCATCC
GAATCCTGCTTCAGAAACTGCGGCCCCCAGATATCAGGAAGAGTGACAGCAGTCCATACTCAAG
GCTAGCCAGGTCCACACTCCTGCTGATCCCCCTGTTTGGAGTACACTACATCATGTTCGCCTTC
TTTCCGGACAATTTTAAGCCTGAAGTGAAGATGGTCTTTGAGCTCGTCGTGGGGTCTTTCCAGG
GTTTTGTGGTGGCTATCCTCTACTGCTTCCTCAATGGTGAGGTGCAGGCGGAGCTGAGGCGGAA
GTGGCGGCGCTGGCACCTGCAGGGCGTCCTGGGCTGGAACCCCAAATACCGGCACCCGTCGGGA
GGCAGCAACGGCGCCACGTGCAGCACGCAGGTTTCCATGCTGACCCGCGTCAGCCCAGGTGCCC
GCCGCTCCTCCAGCTTCCAAGCCGAAGTCTCCCTGGTCTGACCACCAGGATCCCAGGGGCCCAA
GGCGGCCCCTCCCGCCCCTTCCCACTCACCCCGGCAGACGCCGGGGACAGAGGCCTGCCCGGGC
GCGGCCAGCCCCGGCCCTGGGCTCGGAGGCTGCCCCCGGCCCCCTGGTCTCTGGTCCGGACACT
CCTAGAGAACGCAGCCCTAGAGCCTGCCTGGAGCGTTTCTAGCAAGTGAGAGAGATGGGAGCTC
CTCTCCTGGAGGATTGCAGGTGGAACTCAGTCATTAGACTCCTCCTCCAAAGGCCCCCTACGCC
AATCAAGGGCAAAAAGTCTACATACTTTCATCCTGACTCTGCCCCCTGCTGGCTCTTCTGCCCA
ATTGGAGGAAAGCAACCGGTGGATCCTCAAACAACACTGGTGTGACCTGAGGGCAGAAAGGTTC
TGCCCGGGAAGGTCACCAGCACCAACACCACGGTAGTGCCTGAAATTTCACCATTGCTGTCAAG
TTCCTTTGGGTTAAGCATTACCACTCAGGCATTTGACTGAAGATGCAGCTCACTACCCTATTCT
CTCTTTACGCTTAGTTATCAGCTTTTTAAAGTGGGTTATTCTGGAGTTTTTGTTTGGAGAGCAC
ACCTATCTTAGTGGTTCCCCACCGAAGTGGACTGGCCCCTGGGTCAGTCTGGTGGGAGGACGGT
GCAACCCAAGGACTGAGGGACTCTGAAGCCTCTGGGAAATGAGAAGGCAGCCACCAGCGAATGC
TAGGTCTCGGACTAAGCCTACCTGCTCTCCAAGTCTCAGTGGCTTCATCTGTCAAGTGGGATCT
GTCACACCAGCCATACTTATCTCTCTGTGCTGTGGAAGCAACAGGAATCAAGAGCTGCCCTCCT
TGTCCACCCACCTATGTGCCAACTGTTGTAACTAGGCTCAGAGATGTGCACCCATGGGCTCTGA
CAGAAAGCAGATACCTCACCCTGCTACACATACAGGATTTGAACTCAGATCTGTCTGATAGGAA
TGTGAAAGCACGGACTCTTACTGCTAACTTTTGTGTATCGTAACCAGCCAGATCCTCTTGGTTA
TTTGTTTACCACTTGTATTATTAATGCCATTATCCCTGAATCCCCCTTGCCACCCCACCCTCCC
TGGAGTGTGGCTGAGGAGGCCTCCATCTCATGTATCATCTGGATAGGAGCCTGCTGGTCACAGC
CTCCTCTGTCTGCCCTTCACCCCAGTGGCCACTCAGCTTCCTACCCACACCTCTGCCAGAAGAT
CCCCTCAGGACTGCAACAGGCTTGTGCAACAATAAATGTTGGCTTGGATTGGC

hide sequence

Protein Sequences


Protein RefSeqs	NP_001238811	(Get FASTA)	NCBI Sequence Viewer
	NP_001238812	(Get FASTA)	NCBI Sequence Viewer
	NP_001238813	(Get FASTA)	NCBI Sequence Viewer
	NP_001238814	(Get FASTA)	NCBI Sequence Viewer
	NP_004615	(Get FASTA)	NCBI Sequence Viewer
	XP_005265494	(Get FASTA)	NCBI Sequence Viewer
	XP_005265496	(Get FASTA)	NCBI Sequence Viewer
	XP_011532382	(Get FASTA)	NCBI Sequence Viewer
	XP_047304806	(Get FASTA)	NCBI Sequence Viewer
	XP_047304807	(Get FASTA)	NCBI Sequence Viewer
	XP_054203720	(Get FASTA)	NCBI Sequence Viewer
	XP_054203721	(Get FASTA)	NCBI Sequence Viewer
	XP_054203722	(Get FASTA)	NCBI Sequence Viewer
	XP_054203723	(Get FASTA)	NCBI Sequence Viewer
	XP_054203724	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA36802	(Get FASTA)	NCBI Sequence Viewer
	AAA36805	(Get FASTA)	NCBI Sequence Viewer
	AAB60362	(Get FASTA)	NCBI Sequence Viewer
	AAH64424	(Get FASTA)	NCBI Sequence Viewer
	ABQ52416	(Get FASTA)	NCBI Sequence Viewer
	BAC05895	(Get FASTA)	NCBI Sequence Viewer
	BAG36980	(Get FASTA)	NCBI Sequence Viewer
	BAG51813	(Get FASTA)	NCBI Sequence Viewer
	BAG57026	(Get FASTA)	NCBI Sequence Viewer
	BAG57795	(Get FASTA)	NCBI Sequence Viewer
	BAG60398	(Get FASTA)	NCBI Sequence Viewer
	CAA09908	(Get FASTA)	NCBI Sequence Viewer
	CAA53046	(Get FASTA)	NCBI Sequence Viewer
	CAS01788	(Get FASTA)	NCBI Sequence Viewer
	EAW64649	(Get FASTA)	NCBI Sequence Viewer
	EAW64650	(Get FASTA)	NCBI Sequence Viewer
	EAW64651	(Get FASTA)	NCBI Sequence Viewer
	EAW64652	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000327246
	ENSP00000327246.4
	ENSP00000388479.1
	ENSP00000393215.1
	ENSP00000394950
	ENSP00000394950.1
	ENSP00000396204.1
	ENSP00000403478.1
	ENSP00000403680.1
	ENSP00000415013.1
	ENSP00000415371
	ENSP00000415371.2
	ENSP00000445701
	ENSP00000445701.1
GenBank Protein	P32241	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_004615 ⟸ NM_004624
- Peptide Label:	isoform 1 precursor
- UniProtKB:	Q15871 (UniProtKB/Swiss-Prot), G3V0I1 (UniProtKB/Swiss-Prot), F5H1F5 (UniProtKB/Swiss-Prot), B4DGI4 (UniProtKB/Swiss-Prot), B4DEB5 (UniProtKB/Swiss-Prot), B3KPV1 (UniProtKB/Swiss-Prot), A5JUT9 (UniProtKB/Swiss-Prot), Q6P2M6 (UniProtKB/Swiss-Prot), P32241 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRPPSPLPARWLCVLAGALAWALGPAGGQAARLQEECDYVQMIEVQHKQCLEEAQLENETIGCS KMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSCTDEGWTHLEPGPYPIACGLDDKA ASLDEQQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRKLHCTRNYIHMHLFISFILRAAAV FIKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWLLVEGLYLYTLLAVSFFSERKYFW GYILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWIIKGPILTSILVNFILFICIIRILL QKLRPPDIRKSDSSPYSRLARSTLLLIPLFGVHYIMFAFFPDNFKPEVKMVFELVVGSFQGFVV AILYCFLNGEVQAELRRKWRRWHLQGVLGWNPKYRHPSGGSNGATCSTQVSMLTRVSPGARRSS SFQAEVSLV hide sequence

RefSeq Acc Id:

NP_001238811 ⟸ NM_001251882

- Peptide Label:

isoform 2

- Sequence:

show sequence

MIEVQHKQCLEEAQLENETIGCSKMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSC
TDEGWTHLEPGPYPIACGLDDKAASLDEQQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRK
LHCTRNYIHMHLFISFILRAAAVFIKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWL
LVEGLYLYTLLAVSFFSERKYFWGYILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWII
KGPILTSILVNFILFICIIRILLQKLRPPDIRKSDSSPYSRLARSTLLLIPLFGVHYIMFAFFP
DNFKPEVKMVFELVVGSFQGFVVAILYCFLNGEVQAELRRKWRRWHLQGVLGWNPKYRHPSGGS
NGATCSTQVSMLTRVSPGARRSSSFQAEVSLV

hide sequence

RefSeq Acc Id:	NP_001238813 ⟸ NM_001251884
- Peptide Label:	isoform 4
- UniProtKB:	P32241 (UniProtKB/Swiss-Prot), B4DNY6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRAGRRPRLGPWAGGCSKMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSCTDEGWT HLEPGPYPIACGLDDKAASLDEQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRKLHCTRNY IHMHLFISFILRAAAVFIKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWLLVEGLYL YTLLAVSFFSERKYFWGYILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWIIKGPILTS ILVNFILFICIIRILLQKLRPPDIRKSDSSPYSRLARSTLLLIPLFGVHYIMFAFFPDNFKPEV KMVFELVVGSFQGFVVAILYCFLNGEVQAELRRKWRRWHLQGVLGWNPKYRHPSGGSNGATCST QVSMLTRVSPGARRSSSFQAEVSLV hide sequence

RefSeq Acc Id:	NP_001238812 ⟸ NM_001251883
- Peptide Label:	isoform 3
- UniProtKB:	P32241 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTRQRVWMRWAVRQPWSFSNIVSWLTSSGCWWRASTCTPCLPSPSSLSGSTSGGVPSTFTMVWT IARIHFEDYGCWDTINSSLWWIIKGPILTSILVNFILFICIIRILLQKLRPPDIRKSDSSPYSR LARSTLLLIPLFGVHYIMFAFFPDNFKPEVKMVFELVVGSFQGFVVAILYCFLNGEVQAELRRK WRRWHLQGVLGWNPKYRHPSGGSNGATCSTQVSMLTRVSPGARRSSSFQAEVSLV hide sequence

RefSeq Acc Id:	NP_001238814 ⟸ NM_001251885
- Peptide Label:	isoform 5
- UniProtKB:	B4DNY6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRAGRLQEECDYVQMIEVQHKQCLEEAQLENETIGCSKMWDNLTCWPATPRGQVVVLACPLIFK LFSSIQGRNVSRSCTDEGWTHLEPGPYPIACGLDDKAASLDEQQTMFYGSVKTGYTIGYGLSLA TLLVATAILSLFRKLHCTRNYIHMHLFISFILRAAAVFIKDLALFDSGESDQCSEGSVGCKAAM VFFQYCVMANFFWLLVEGLYLYTLLAVSFFSERKYFWGYILIGWGVPSTFTMVWTIARIHFEDY GCWDTINSSLWWIIKGPILTSILVNFILFICIIRILLQKLRPPDIRKSDSSPYSRLARSTLLLI PLFGVHYIMFAFFPDNFKPEVKMVFELVVGSFQGFVVAILYCFLNGEVQAELRRKWRRWHLQGV LGWNPKYRHPSGGSNGATCSTQVSMLTRVSPGARRSSSFQAEVSLV hide sequence

RefSeq Acc Id:

XP_005265494 ⟸ XM_005265437

- Peptide Label:

isoform X1

- Sequence:

show sequence

MRPPSPLPARWLCVLAGALAWALGPAGGQAARLQEECDYVQMIEVQHKQCLEEAQLENETIGCS
KMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSCTDEGWTHLEPGPYPIACGLDDKA
ASLDEQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRKLHCTRNYIHMHLFISFILRAAAVF
IKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWLLVEGLYLYTLLAVSFFSERKYFWG
YILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWIIKGPILTSILVNFILFICIIRILLQ
KLRPPDIRKSDSSPYSRLARSTLLLIPLFGVHYIMFAFFPDNFKPEVKMVFELVVGSFQGFVVA
ILYCFLNGEVQAELRRKWRRWHLQGVLGWNPKYRHPSGGSNGATCSTQVSMLTRVSPGARRSSS
FQAEVSLV

hide sequence

RefSeq Acc Id:

XP_005265496 ⟸ XM_005265439

- Peptide Label:

isoform X2

- Sequence:

show sequence

MRAGRRPRLGPWAGGCSKMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSCTDEGWT
HLEPGPYPIACGLDDKAASLDEQQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRKLHCTRN
YIHMHLFISFILRAAAVFIKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWLLVEGLY
LYTLLAVSFFSERKYFWGYILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWIIKGPILT
SILVNFILFICIIRILLQKLRPPDIRKSDSSPYSRLARSTLLLIPLFGVHYIMFAFFPDNFKPE
VKMVFELVVGSFQGFVVAILYCFLNGEVQAELRRKWRRWHLQGVLGWNPKYRHPSGGSNGATCS
TQVSMLTRVSPGARRSSSFQAEVSLV

hide sequence

RefSeq Acc Id:

XP_011532382 ⟸ XM_011534080

- Peptide Label:

isoform X3

- Sequence:

show sequence

MRPPSPLPARWLCVLAGALAWALGPAGGQAARLQEECDYVQMIEVQHKQCLEEAQLENETIGCS
KMWDNLTCWPATPRGQVVVLACPLIFKLFSSIQGRNVSRSCTDEGWTHLEPGPYPIACGLDDKA
ASLDEQQTMFYGSVKTGYTIGYGLSLATLLVATAILSLFRKLHCTRNYIHMHLFISFILRAAAV
FIKDLALFDSGESDQCSEGSVGCKAAMVFFQYCVMANFFWLLVEGLYLYTLLAVSFFSERKYFW
GYILIGWGVPSTFTMVWTIARIHFEDYGCWDTINSSLWWIIKGPILTSILVNFILFICIIRILL
QKLRPPDIRKSDSSPYSYASAAKPGSSRGHR

hide sequence

Ensembl Acc Id:

ENSP00000415371 ⟸ ENST00000438259

Ensembl Acc Id:

ENSP00000403478 ⟸ ENST00000439731

Ensembl Acc Id:

ENSP00000415013 ⟸ ENST00000450274

Ensembl Acc Id:

ENSP00000403680 ⟸ ENST00000439910

Ensembl Acc Id:

ENSP00000445701 ⟸ ENST00000543411

Ensembl Acc Id:

ENSP00000327246 ⟸ ENST00000325123

Ensembl Acc Id:

ENSP00000388479 ⟸ ENST00000443646

Ensembl Acc Id:

ENSP00000396204 ⟸ ENST00000446673

Ensembl Acc Id:

ENSP00000394950 ⟸ ENST00000433647

Ensembl Acc Id:

ENSP00000393215 ⟸ ENST00000436487

RefSeq Acc Id:	XP_047304806 ⟸ XM_047448850
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047304807 ⟸ XM_047448851
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054203720 ⟸ XM_054347745
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054203721 ⟸ XM_054347746
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054203722 ⟸ XM_054347747
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054203723 ⟸ XM_054347748
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054203724 ⟸ XM_054347749
- Peptide Label:	isoform X5

Protein Domains

G-protein coupled receptors family 2 profile

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P32241-F1-model_v2	AlphaFold	P32241	1-457	view protein structure

Promoters

RGD ID:

6864052

Promoter ID:

EPDNEW_H5191

Type:

initiation region

Name:

VIPR1_1

Description:

vasoactive intestinal peptide receptor 1

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	3	42,502,643 - 42,502,703	EPDNEW

RGD ID:

6801937

Promoter ID:

HG_KWN:44575

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_004624, OTTHUMT00000343239, OTTHUMT00000343240, OTTHUMT00000343242, OTTHUMT00000343322, OTTHUMT00000343323, OTTHUMT00000343324, OTTHUMT00000343328

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	3	42,518,776 - 42,519,276 (+)	MPROMDB

RGD ID:

6801936

Promoter ID:

HG_KWN:44577

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

NB4

Transcripts:

OTTHUMT00000343417

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	3	42,543,311 - 42,543,811 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12694	AgrOrtholog
COSMIC	VIPR1	COSMIC
Ensembl Genes	ENSG00000114812	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000325123	ENTREZGENE
	ENST00000325123.5	UniProtKB/Swiss-Prot
	ENST00000433647	ENTREZGENE
	ENST00000433647.5	UniProtKB/Swiss-Prot
	ENST00000436487	ENTREZGENE
	ENST00000436487.5	UniProtKB/TrEMBL
	ENST00000438259	ENTREZGENE
	ENST00000438259.6	UniProtKB/Swiss-Prot
	ENST00000439731.5	UniProtKB/TrEMBL
	ENST00000439910.5	UniProtKB/TrEMBL
	ENST00000443646.5	UniProtKB/TrEMBL
	ENST00000446673.5	UniProtKB/TrEMBL
	ENST00000450274.5	UniProtKB/TrEMBL
	ENST00000543411	ENTREZGENE
	ENST00000543411.5	UniProtKB/Swiss-Prot
Gene3D-CATH	4.10.1240.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Rhodopsin 7-helix transmembrane proteins	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000114812	GTEx
HGNC ID	HGNC:12694	ENTREZGENE
Human Proteome Map	VIPR1	Human Proteome Map
InterPro	GPCR_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_extracell_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_extracellular_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_secretin-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_secretin-like_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_VIP_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_2_VIP_rcpt_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7433	UniProtKB/Swiss-Prot
NCBI Gene	7433	ENTREZGENE
OMIM	192321	OMIM
PANTHER	PDF RECEPTOR-LIKE PROTEIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VASOACTIVE INTESTINAL POLYPEPTIDE RECEPTOR 1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	7tm_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HRM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37313	PharmGKB
PRINTS	GPCRSECRETIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VASOACTVEIPR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VIP1RECEPTOR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F2_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	HormR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Family A G protein-coupled receptor-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF111418	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A5JUT9	ENTREZGENE
	B3KPV1	ENTREZGENE
	B4DEB5	ENTREZGENE
	B4DGI4	ENTREZGENE
	B4DNY6	ENTREZGENE, UniProtKB/TrEMBL
	C9JDT8_HUMAN	UniProtKB/TrEMBL
	C9JH33_HUMAN	UniProtKB/TrEMBL
	F2Z2U6_HUMAN	UniProtKB/TrEMBL
	F5H1F5	ENTREZGENE
	G3V0I1	ENTREZGENE
	P32241	ENTREZGENE
	Q15871	ENTREZGENE
	Q6P2M6	ENTREZGENE
	VIPR1_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A5JUT9	UniProtKB/Swiss-Prot
	B3KPV1	UniProtKB/Swiss-Prot
	B4DEB5	UniProtKB/Swiss-Prot
	B4DGI4	UniProtKB/Swiss-Prot
	F5H1F5	UniProtKB/Swiss-Prot
	G3V0I1	UniProtKB/Swiss-Prot
	Q15871	UniProtKB/Swiss-Prot
	Q6P2M6	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)

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