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Gene: GLP2R (glucagon like peptide 2 receptor) Homo sapiens

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Symbol:

GLP2R

Name:

glucagon like peptide 2 receptor

RGD ID:

731561

HGNC Page

HGNC:4325

Description:

Predicted to enable glucagon receptor activity and peptide hormone binding activity. Predicted to be involved in adenylate cyclase-modulating G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

GLP-2 receptor; GLP-2-R; GLP-2R; glucagon-like peptide 2 receptor

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	17	9,825,924 - 9,892,099 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	9,822,206 - 9,892,099 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	9,729,241 - 9,795,416 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	9,670,106 - 9,733,747 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	9,670,105 - 9,733,747	NCBI
Celera	17	9,760,703 - 9,824,336 (+)	NCBI		Celera
Cytogenetic Map	17	p13.1	NCBI
HuRef	17	9,629,750 - 9,693,383 (+)	NCBI		HuRef
CHM1_1	17	9,739,411 - 9,803,035 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	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

congenital myopathy 6 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

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

1,2-dichloroethane (ISO)

1,2-dimethylhydrazine (ISO)

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

ammonium chloride (ISO)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

CGP 52608 (EXP)

cisplatin (EXP)

cocaine (ISO)

crocidolite asbestos (ISO)

dexamethasone (EXP)

doxorubicin (ISO)

folic acid (ISO)

indometacin (EXP)

methotrexate (EXP)

nickel sulfate (EXP)

paracetamol (EXP)

perfluorooctane-1-sulfonic acid (ISO)

perfluorooctanoic acid (ISO)

silicon dioxide (EXP)

sodium arsenite (EXP)

titanium dioxide (ISO)

trovafloxacin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

adenylate cyclase-modulating G protein-coupled receptor signaling pathway (IBA,IEA,ISO,TAS)

cell surface receptor signaling pathway (IEA)

cellular response to glucagon stimulus (IEA)

G protein-coupled receptor signaling pathway (IEA)

positive regulation of cell population proliferation (TAS)

Cellular Component

membrane (IEA,TAS)

plasma membrane (IBA,IEA,TAS)

Molecular Function

G protein-coupled receptor activity (IEA,TAS)

glucagon receptor activity (IBA,IEA,ISO)

peptide hormone binding (IBA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Prototypic G protein-coupled receptor for the intestinotrophic factor glucagon-like peptide 2.	Munroe DG, etal., Proc Natl Acad Sci U S A 1999 Feb 16;96(4):1569-73.
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:10982769	PMID:11238747	PMID:11738243	PMID:12477932	PMID:15471943	PMID:15544847	PMID:15670850	PMID:15817468	PMID:16401478	PMID:16448646	PMID:18240029	PMID:18829546
PMID:19861958	PMID:19913121	PMID:20379614	PMID:20468064	PMID:20628086	PMID:20800603	PMID:21167157	PMID:21326311	PMID:21873635	PMID:22951144	PMID:24875097	PMID:24990862
PMID:28337026	PMID:28514806	PMID:28700943	PMID:28746825	PMID:30409537	PMID:31391242	PMID:32191643	PMID:33239759	PMID:33544567	PMID:34174312

Genomics

Comparative Map Data

GLP2R
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	9,822,206 - 9,892,099 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	9,729,241 - 9,795,416 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	9,670,106 - 9,733,747 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	9,670,105 - 9,733,747	NCBI
Celera	17	9,760,703 - 9,824,336 (+)	NCBI		Celera
Cytogenetic Map	17	p13.1	NCBI
HuRef	17	9,629,750 - 9,693,383 (+)	NCBI		HuRef
CHM1_1	17	9,739,411 - 9,803,035 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI		T2T-CHM13v2.0

Glp2r
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	67,554,877 - 67,661,979 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	67,552,328 - 67,661,979 (-)	Ensembl		GRCm39 Ensembl
GRCm38	11	67,664,156 - 67,771,184 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	67,661,502 - 67,771,153 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	67,519,932 - 67,584,655 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	67,522,625 - 67,587,348 (-)	NCBI		MGSCv36	mm8
MGSCv36	11	68,292,730 - 68,351,279 (-)	NCBI		MGSCv36	mm8
Celera	11	74,649,125 - 74,715,011 (-)	NCBI		Celera
Cytogenetic Map	11	B3	NCBI
cM Map	11	41.13	NCBI

Glp2r
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	52,901,707 - 52,964,961 (-)	NCBI		GRCr8
mRatBN7.2	10	52,402,748 - 52,466,012 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	52,402,748 - 52,466,012 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	57,060,278 - 57,128,159 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	56,549,284 - 56,617,168 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	52,059,289 - 52,122,389 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	54,260,290 - 54,323,839 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	54,260,290 - 54,323,439 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	54,006,866 - 54,070,157 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	54,423,127 - 54,487,060 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	54,436,749 - 54,500,683 (-)	NCBI
Celera	10	51,583,978 - 51,647,093 (-)	NCBI		Celera
Cytogenetic Map	10	q24	NCBI

Glp2r
(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_004955467	7,242,180 - 7,296,713 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955467	7,239,547 - 7,308,809 (-)	NCBI	ChiLan1.0	ChiLan1.0

GLP2R
(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	19	63,858,957 - 63,925,236 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	68,665,619 - 68,734,758 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	41,764,686 - 41,830,966 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	46,508,568 - 46,574,695 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	46,508,568 - 46,574,695 (-)	Ensembl	panpan1.1		panPan2

GLP2R
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	5	34,267,270 - 34,317,525 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	5	34,266,966 - 34,318,472 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	5	34,403,170 - 34,454,055 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	5	34,371,193 - 34,421,655 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	5	34,371,032 - 34,421,253 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	5	34,336,983 - 34,387,401 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	5	34,295,062 - 34,345,268 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	5	34,475,553 - 34,525,955 (+)	NCBI		UU_Cfam_GSD_1.0

Glp2r
(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_024405602	49,313,268 - 49,393,453 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936595	2,787,963 - 2,868,051 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936595	2,787,978 - 2,868,033 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

GLP2R
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	54,680,057 - 54,738,102 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	54,680,047 - 54,747,338 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	57,438,490 - 57,493,322 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

GLP2R
(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	16	9,161,241 - 9,228,965 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	9,162,107 - 9,227,581 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666059	12,112,708 - 12,181,573 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Glp2r
(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_004624786	12,260,029 - 12,324,632 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624786	12,260,029 - 12,325,838 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in GLP2R
44 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17p13.1(chr17:7750804-10112969)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052460]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052460]\|See cases [RCV000052460]	Chr17:7750804..10112969 [GRCh38] Chr17:7654122..10016286 [GRCh37] Chr17:7594847..9957011 [NCBI36] Chr17:17p13.1	pathogenic
GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3	copy number gain	See cases [RCV000134851]	Chr17:5732953..12095349 [GRCh38] Chr17:5636273..11998666 [GRCh37] Chr17:5576997..11939391 [NCBI36] Chr17:17p13.2-12	pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3	copy number gain	See cases [RCV000138531]	Chr17:162016..12343901 [GRCh38] Chr17:45835..12247218 [GRCh37] Chr17:11807..12187943 [NCBI36] Chr17:17p13.3-12	pathogenic
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	copy number gain	See cases [RCV000142236]	Chr17:150732..14764202 [GRCh38] Chr17:525..14667519 [GRCh37] Chr17:525..14608244 [NCBI36] Chr17:17p13.3-12	pathogenic
GRCh38/hg38 17p13.1-12(chr17:9701182-11983353)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207166]	Chr17:9701182..11983353 [GRCh38] Chr17:9604499..11886670 [GRCh37] Chr17:17p13.1-12	uncertain significance
Single allele	complex	Breast ductal adenocarcinoma [RCV000207129]	Chr17:9586165..16325968 [GRCh37] Chr17:17p13.1-11.2	uncertain significance
GRCh37/hg19 17p13.1(chr17:7929776-9995862)x3	copy number gain	See cases [RCV000447853]	Chr17:7929776..9995862 [GRCh37] Chr17:17p13.1	uncertain significance
GRCh37/hg19 17p13.1(chr17:9751024-9804265)x3	copy number gain	See cases [RCV000448454]	Chr17:9751024..9804265 [GRCh37] Chr17:17p13.1	uncertain significance
GRCh37/hg19 17p13.1(chr17:7431013-9868179)x3	copy number gain	See cases [RCV000511388]	Chr17:7431013..9868179 [GRCh37] Chr17:17p13.1	uncertain significance
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3	copy number gain	See cases [RCV000511786]	Chr17:525..15027737 [GRCh37] Chr17:17p13.3-12	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3	copy number gain	not provided [RCV000683866]	Chr17:525..11186432 [GRCh37] Chr17:17p13.3-12	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
NM_004246.3(GLP2R):c.764A>C (p.Glu255Ala)	single nucleotide variant	not provided [RCV000972917]	Chr17:9857575 [GRCh38] Chr17:9760892 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.291C>T (p.Asn97=)	single nucleotide variant	not provided [RCV000965369]	Chr17:9836384 [GRCh38] Chr17:9739701 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.1543G>A (p.Ala515Thr)	single nucleotide variant	not provided [RCV000973548]	Chr17:9889586 [GRCh38] Chr17:9792903 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.1568G>A (p.Arg523His)	single nucleotide variant	not provided [RCV000962467]	Chr17:9889611 [GRCh38] Chr17:9792928 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.1414C>T (p.Arg472Trp)	single nucleotide variant	not provided [RCV000967436]	Chr17:9889457 [GRCh38] Chr17:9792774 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.627G>A (p.Thr209=)	single nucleotide variant	not provided [RCV000962466]	Chr17:9857438 [GRCh38] Chr17:9760755 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.1565C>A (p.Ala522Glu)	single nucleotide variant	not specified [RCV004289289]	Chr17:9889608 [GRCh38] Chr17:9792925 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.65A>T (p.His22Leu)	single nucleotide variant	not provided [RCV000962465]	Chr17:9826128 [GRCh38] Chr17:9729445 [GRCh37] Chr17:17p13.1	benign
NM_004246.3(GLP2R):c.271C>G (p.Pro91Ala)	single nucleotide variant	not provided [RCV000910307]	Chr17:9833888 [GRCh38] Chr17:9737205 [GRCh37] Chr17:17p13.1	benign
NC_000017.11:g.(?_9794928)_(10547930_?)del	deletion	Myopathy, proximal, and ophthalmoplegia [RCV001032635]	Chr17:9698245..10451247 [GRCh37] Chr17:17p13.1	pathogenic
GRCh37/hg19 17p13.1(chr17:7929776-9995862)	copy number gain	not specified [RCV002052588]	Chr17:7929776..9995862 [GRCh37] Chr17:17p13.1	uncertain significance
GRCh37/hg19 17p13.1(chr17:9695852-10118691)x3	copy number gain	not provided [RCV002472693]	Chr17:9695852..10118691 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1358G>A (p.Arg453His)	single nucleotide variant	not specified [RCV004136728]	Chr17:9889401 [GRCh38] Chr17:9792718 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1577G>A (p.Arg526Gln)	single nucleotide variant	not specified [RCV004172889]	Chr17:9889620 [GRCh38] Chr17:9792937 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.11G>A (p.Gly4Glu)	single nucleotide variant	not specified [RCV004120339]	Chr17:9826074 [GRCh38] Chr17:9729391 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.583C>G (p.Leu195Val)	single nucleotide variant	not specified [RCV004153863]	Chr17:9854573 [GRCh38] Chr17:9757890 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1483C>A (p.Pro495Thr)	single nucleotide variant	not specified [RCV004129595]	Chr17:9889526 [GRCh38] Chr17:9792843 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1597T>A (p.Cys533Ser)	single nucleotide variant	not specified [RCV004116398]	Chr17:9889640 [GRCh38] Chr17:9792957 [GRCh37] Chr17:17p13.1	likely benign
NM_004246.3(GLP2R):c.1016T>G (p.Ile339Ser)	single nucleotide variant	not specified [RCV004205435]	Chr17:9862050 [GRCh38] Chr17:9765367 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.67G>A (p.Glu23Lys)	single nucleotide variant	not specified [RCV004241749]	Chr17:9826130 [GRCh38] Chr17:9729447 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.689T>C (p.Val230Ala)	single nucleotide variant	not specified [RCV004214179]	Chr17:9857500 [GRCh38] Chr17:9760817 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1122G>A (p.Met374Ile)	single nucleotide variant	not specified [RCV004132590]	Chr17:9870812 [GRCh38] Chr17:9774129 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.671G>A (p.Arg224Lys)	single nucleotide variant	not specified [RCV004100001]	Chr17:9857482 [GRCh38] Chr17:9760799 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.697G>A (p.Val233Ile)	single nucleotide variant	not specified [RCV004166993]	Chr17:9857508 [GRCh38] Chr17:9760825 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.985G>A (p.Gly329Arg)	single nucleotide variant	not specified [RCV004271311]	Chr17:9861198 [GRCh38] Chr17:9764515 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1117C>A (p.Gln373Lys)	single nucleotide variant	not specified [RCV004284723]	Chr17:9870807 [GRCh38] Chr17:9774124 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.964C>T (p.Arg322Cys)	single nucleotide variant	not specified [RCV004253453]	Chr17:9861177 [GRCh38] Chr17:9764494 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1372C>T (p.Arg458Cys)	single nucleotide variant	not specified [RCV004272056]	Chr17:9889415 [GRCh38] Chr17:9792732 [GRCh37] Chr17:17p13.1	uncertain significance
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3	copy number gain	Chromosome 17p13.3 duplication syndrome [RCV003327726]	Chr17:165730..11404096 [GRCh38] Chr17:17p13.3-12	pathogenic
NM_004246.3(GLP2R):c.512G>A (p.Arg171His)	single nucleotide variant	not specified [RCV004339699]	Chr17:9854502 [GRCh38] Chr17:9757819 [GRCh37] Chr17:17p13.1	likely benign
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	copy number gain	not specified [RCV003987215]	Chr17:525..21510992 [GRCh37] Chr17:17p13.3-11.2	pathogenic
NM_004246.3(GLP2R):c.31G>A (p.Gly11Arg)	single nucleotide variant	not specified [RCV004393214]	Chr17:9826094 [GRCh38] Chr17:9729411 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.449C>T (p.Thr150Met)	single nucleotide variant	not specified [RCV004393216]	Chr17:9842561 [GRCh38] Chr17:9745878 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.893G>A (p.Arg298Gln)	single nucleotide variant	not specified [RCV004393218]	Chr17:9860069 [GRCh38] Chr17:9763386 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1373G>A (p.Arg458His)	single nucleotide variant	not specified [RCV004393212]	Chr17:9889416 [GRCh38] Chr17:9792733 [GRCh37] Chr17:17p13.1	likely benign
NM_004246.3(GLP2R):c.43G>A (p.Ala15Thr)	single nucleotide variant	not specified [RCV004393215]	Chr17:9826106 [GRCh38] Chr17:9729423 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.781C>T (p.Arg261Cys)	single nucleotide variant	not specified [RCV004393217]	Chr17:9859957 [GRCh38] Chr17:9763274 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1415G>A (p.Arg472Gln)	single nucleotide variant	not specified [RCV004393213]	Chr17:9889458 [GRCh38] Chr17:9792775 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1361T>G (p.Phe454Cys)	single nucleotide variant	not specified [RCV004629757]	Chr17:9889404 [GRCh38] Chr17:9792721 [GRCh37] Chr17:17p13.1	uncertain significance
NM_004246.3(GLP2R):c.1561C>G (p.His521Asp)	single nucleotide variant	not specified [RCV004629758]	Chr17:9889604 [GRCh38] Chr17:9792921 [GRCh37] Chr17:17p13.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2420
Count of miRNA genes:	1070
Interacting mature miRNAs:	1318
Transcripts:	ENST00000262441, ENST00000304773, ENST00000458005, ENST00000574745
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

SHGC-142190

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	9,768,843 - 9,769,169	UniSTS	GRCh37
Build 36	17	9,709,568 - 9,709,894	RGD	NCBI36
Celera	17	9,800,163 - 9,800,489	RGD
Cytogenetic Map	17	p13.3	UniSTS
HuRef	17	9,669,191 - 9,669,517	UniSTS
TNG Radiation Hybrid Map	17	6093.0	UniSTS

GLP2R_7942

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	9,792,696 - 9,793,191	UniSTS	GRCh37
Build 36	17	9,733,421 - 9,733,916	RGD	NCBI36
Celera	17	9,824,010 - 9,824,505	RGD
HuRef	17	9,693,057 - 9,693,552	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1204	2332	2689	2181	4485	1579	2050	3	551	883	404	1920	5791	5321	15	3571	631	1575	1397	158

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_004246	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005256861	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025340	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025341	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC026591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF105367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307283	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK314269	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC019818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC041176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC043390	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC096264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471108	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	GQ891498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000262441 ⟹ ENSP00000262441

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	9,825,924 - 9,892,099 (+)	Ensembl

Ensembl Acc Id:

ENST00000304773 ⟹ ENSP00000303605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	9,842,485 - 9,860,071 (+)	Ensembl

Ensembl Acc Id:

ENST00000458005 ⟹ ENSP00000404471

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	9,825,904 - 9,866,977 (+)	Ensembl

Ensembl Acc Id:

ENST00000574745 ⟹ ENSP00000458242

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	9,822,206 - 9,890,034 (+)	Ensembl

RefSeq Acc Id:

NM_004246 ⟹ NP_004237

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI
GRCh37	17	9,729,152 - 9,794,269 (+)	NCBI
Build 36	17	9,670,106 - 9,733,747 (+)	NCBI Archive
HuRef	17	9,629,750 - 9,693,383 (+)	ENTREZGENE
CHM1_1	17	9,738,898 - 9,805,432 (+)	NCBI
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI

Sequence:

show sequence

AGACACTCTCGGCGCAGCGTGGAGAGGATTTGTGCAAACATTTCCTCTGTGGACCAAGAGGAAT
GCAAGAGGAGGCTGCCTGCGGTGCATCTTGGACGGCTAGAGAGATGTACCCCTACTTGTGAAGG
TGCACGAGGAAGATGAAGCTGGGATCGAGCAGGGCAGGGCCTGGGAGAGGAAGCGCGGGACTCC
TGCCTGGCGTCCACGAGCTGCCCATGGGCATCCCTGCCCCCTGGGGGACCAGTCCTCTCTCCTT
CCACAGGAAGTGCTCTCTCTGGGCCCCTGGGAGGCCCTTCCTCACTCTGGTCCTGCTGGTTTCC
ATCAAGCAAGTTACAGGATCCCTCCTTGAGGAAACGACTCGGAAGTGGGCTCAGTACAAACAGG
CATGTCTGAGAGACTTACTCAAGGAACCTTCTGGCATATTTTGTAACGGGACATTTGATCAGTA
CGTGTGTTGGCCTCATTCTTCTCCTGGAAATGTCTCTGTACCCTGCCCTTCATACTTACCTTGG
TGGAGTGAAGAGAGCTCAGGAAGGGCCTACAGACACTGCTTGGCTCAGGGGACTTGGCAGACGA
TAGAGAACGCCACGGATATTTGGCAGGATGACTCCGAATGCTCCGAGAACCACAGCTTCAAGCA
AAACGTGGATCGTTATGCCTTGCTGTCAACCTTGCAGCTGATGTACACCGTGGGATACTCCTTC
TCTCTTATCTCCCTCTTCCTGGCTCTCACCCTCCTCTTGTTTCTTCGAAAACTCCACTGCACGC
GCAACTACATCCACATGAACTTGTTTGCTTCTTTCATCCTGAGAACCCTGGCTGTACTGGTGAA
GGACGTCGTCTTCTACAACTCTTACTCCAAGAGGCCTGACAATGAGAATGGGTGGATGTCCTAC
CTGTCAGAGATGTCCACCTCCTGCCGCTCAGTCCAGGTTCTCTTGCATTACTTTGTGGGTGCCA
ATTACTTATGGCTGCTGGTTGAAGGCCTCTACCTCCACACGCTGCTGGAGCCCACAGTGCTTCC
TGAGAGGCGGCTGTGGCCCAGATACCTGCTGTTGGGTTGGGCCTTCCCTGTGCTATTTGTTGTA
CCCTGGGGTTTCGCCCGTGCACACCTGGAGAACACAGGGTGCTGGACAACAAATGGGAATAAGA
AAATCTGGTGGATCATCCGAGGACCCATGATGCTCTGTGTAACAGTCAATTTCTTCATCTTCCT
GAAAATTCTCAAGCTTCTCATTTCTAAGCTCAAAGCTCATCAAATGTGCTTCAGAGATTATAAA
TACAGATTGGCAAAATCAACACTGGTCCTCATTCCTTTATTGGGCGTTCATGAGATCCTCTTCT
CTTTCATCACTGATGATCAAGTTGAAGGATTTGCAAAACTTATACGACTTTTCATTCAGTTGAC
ACTGAGCTCCTTTCATGGGTTCCTGGTGGCCTTGCAGTATGGTTTTGCCAATGGAGAGGTGAAG
GCTGAGCTGCGGAAATACTGGGTCCGCTTCTTGCTAGCCCGCCACTCAGGCTGCAGAGCCTGTG
TCCTGGGGAAGGACTTCCGGTTCCTAGGAAAATGTCCCAAGAAGCTCTCGGAAGGAGATGGCGC
TGAGAAGCTTCGGAAGCTGCAGCCCTCACTTAACAGTGGGCGGCTCCTACATCTAGCCATGCGA
GGTCTTGGGGAGCTGGGCGCCCAGCCCCAACAGGACCATGCACGCTGGCCCCGGGGCAGCAGCC
TGTCCGAGTGCAGTGAGGGGGATGTCACCATGGCCAACACCATGGAGGAGATTCTGGAAGAGAG
TGAGATCTAGGGTGGAGTTCCACCACCCTGGCTCTGCTCCCAGGGACTCTTGAGGGGGCCCAGG
AAGAGGAAGCAAAGCAGGACACACGTTGCTGGGCACGGAATCATTCTCGTTCCATTCACCATGC
CACTTTGATATGAAAGCTATCACAAGGTTCTTCAAGCTCTGTATGAAAGAGGCTGTGTGTCATG
CTCACAGCCTCTGCCTGCTCTTCTCATCCTAATAACCCCCACCAGTGTGTTTTCCACAATGCCC
ACCAGACCCTAGGGCCTGGCTCTAAATTCAAGCCAATGAAGTCCCACCATGAAGAGAGGTCTCC
TGTTATAGAGAAGCCAGCCAATATCTCTTCCTTTATCCCTTGGGGTGCATGCTTTCCATCTGAG
GTTGGGTTTAGGGTGCGTGAAAACCTCCTAGGAAGCTTTTAAAATGCAGAATCCTAGACTTGTG
GCTAAGATTCTAAGACAGTGAGTCTGGGACCATGGCCAGGAATTGGAGCTGTTTAATAAGCATC
CCAGGTAATTCTGCTGCAAGCCCACCCTTGGAGAACACTGGGCAGGGTGAGAGGGAGCTAGAAG
CGCCCCCATGTGGCCATGGCAGGATGCTGCAAGAGACAGTCTGCTCTCCCAGGTCAGCTGGGGT
GTGCCTGCCCTCCTTGGAGAGTATGTAACTCCACCCACCAGAGTGCCACTCCTCTCTGCTCTTC
CTCTCCTATCAAGTCTTGCCTCTCTCTCTCTTTGCCTCAGTTCTCTGTCCCTGCACAGCAGGAG
TTCTGCTTGATCCTCCCTTTGAGGATTGGCCCCAGTGCCTGGGGACCCTCTGAATGTCGTCTTT
GGTCTGTTCCTCTCCTTTCTGGCTCTATCTACCTTTCTGAGTTTGGCTTCTACCAGCCTGATTT
ACACTACCATTCTCTTGGGGCAAGGAATGTCCCCACCATTTTTGGTTTGCCATTGATGCATTGA
TTGTCACACCTGTTGTCCCAGGAAGTTGACCTATAACTCTCCATGGCCAGAGTCCCTGCTGATC
AGAATTCAATTTGCCCAGTGGGAATAAATACTGAAAGCAGGAGGGCCCAGGTAAAGCAATAGGA
GTTTGGCTGGATCTGGACATGCCCAGGGTGGCTCTGAGAGATCCAAGACTTTGCATCCACCAGC
CTGTGGGATCTTTCCTGCCTACTGTGACCCATGGAGGCTGAGGAGGGCCCAGGCAGTTGGGGTC
AGGCTCAATGACTGAAAGTATAGGGCAAGAGGCTGTAGGAAGATCAAGGGATGGACATCCTTTG
GAAACAGTGTGTTAATGCACAGGAGTGTCACTTTCATGGTATGTAAAATGCATGTGTACGTGGG
TGGGGTATGTTGCTATGGGACTAAATACCACCTTGTCTTCGGGGGAGTCAGTTTGATACTCCTC
AAGCAGGGCTGCCATATTTAGCAAACAAAAACAAGGTACTCAATTAAATTTGAATTTCAGACAA
ATAGTCTTCTTGTATAAGTATATCCCATGGGCATATTTAATCTGAGATTGGAATTCAATCATGC
ATCTTGTCTTTTACTGGCATCTCTGTTTTCAAGGATACTTTGCCACAGGGCTGGGACTAGGGTG
AAATAATCAAGGCACTCATCTCTAAAAAGCTCAAAGTAAATGATCAAAATAAATCATATTTTAA
TGCAATATTCTAAAAAAACAAATTAACAAACTACAGCCCATGAGCCATTTATAGAAATGAAATT
TGATTGGAGCCAGGGGCAGGATAAGGGTGAGGCAGGAGAGGCCAGCTCTTGCAAGTGCAGGCTC
TGGTCCTGACTTTCAAATGTTGTCTATGAGGGACTTTTAATGTGAATTTTTATTTTTAGACAAT
TGCATTAAAATGTTATTTATATTGACTATGGGGACTTTTGGGGCCCCCTTAAATTTTGCACTTG
AAATGGGATCCCCACTTGTGTCACCCCATAGTCCAGCCCTGGTTTTAGGATGGGGATGGAGGCA
AAGGCATCAGGCAAGTAATGAAGCAAAGGTTTATTTTTTGGTGTCCAGATTATCCATAGCTCAG
TCATGAAAATCTATGTCTTTCTATTTTTCTCCTTTCTGCAAATGTCCCTGCCTCGGCTCATCAG
CCAATTAGCTCCTAGAAAGCTGGGGTCATCTCGTATTCCCAGCAAGTACCCAGCACAGTGCCGG
TTCAGAGCAGGTGCTCCACACACATTCCTGGAATGAGACAGCACAGAAATGGCTCTCGGGAGCC
TCGGATGCTGCTGGGAGTAAGTGATCCAGGACCTTACCGCTAAGAGGAGAAACTTTTTTTCAAA
GCATTTATAAATACTCCCTCCACCCCTCACTCCACAAATGGGGTGATCAACACTTACTGCTTGC
TCTTGTTCTGCTAATGATTAAAACAAGTTTATTTAA

hide sequence

RefSeq Acc Id:

XM_011524077 ⟹ XP_011522379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI

Sequence:

show sequence

GCAACCACCTCTCCTGCAGTCTCTGCATAAACAGGACCCAGAGGAGATTTTGCCTTTGTGGTTA
GCCTCAGCCCAGCCTGGACAAGCTTAATGCCTTAGAAAGAAATACCCTGCCTCAAAAAGACACC
TGCCTCTAAACTGGCTCGAGCCCCATCGCCTTCTGCCAGCCATTCCTCTGTAGCTCGAACCCCA
GCCTGTCTCAGCCAGCTTCGTGCATTGAGCAGAACCTTCAGGGTGGAGCCCGCTGACCGCCTTG
TTCTTTCTCCTCAGCCTGTCAAGGAAGTCCCAGAAAGCACAGCTGACTTAGGGAAGGTCTGGGA
AAAATCTCCCTGCTTTTGGGGGGGCAGGGGCGGGGGATGAGCCAGGGCCGAGAAGGAACTCTGA
AGACTCCGTAGATTGCTCTAGACCGCCTCAGACACTCTCGGCGCAGCGTGGAGAGGATTTGTGC
AAACATTTCCTCTGTGGACCAAGAGGAATGCAAGAGGAGGCTGCCTGCGGTGCATCTTGGACGG
CTAGAGAGATGTACCCCTACTTGTGAAGGTGCACGAGGAAGATGAAGCTGGGATCGAGCAGGGC
AGGGCCTGGGAGAGGAAGCGCGGGACTCCTGCCTGGCGTCCACGAGCTGCCCATGGGCATCCCT
GCCCCCTGGGGGACCAGTCCTCTCTCCTTCCACAGGAAGTGCTCTCTCTGGGCCCCTGGGAGGC
CCTTCCTCACTCTGGTCCTGCTGGTTTCCATCAAGCAAGTTACAGGATCCCTCCTTGAGGAAAC
GACTCGGAAGTGGGCTCAGTACAAACAGGCATGTCTGAGAGACTTACTCAAGGAACCTTCTGGC
ATATTTTGTAACGGGACATTTGATCAGTACGTGTGTTGGCCTCATTCTTCTCCTGGAAATGTCT
CTGTACCCTGCCCTTCATACTTACCTTGGTGGAGTGAAGACCACCAGCAAATACAAGGACAACT
AAAACTGTTCTCAGGAAAGATAAGTGGTTACAAGCTCCAGGCAAAACAAGAGAGCTCAGGAAGG
GCCTACAGACACTGCTTGGCTCAGGGGACTTGGCAGACGATAGAGAACGCCACGGATATTTGGC
AGGATGACTCCGAATGCTCCGAGAACCACAGCTTCAAGCAAAACGTGGATCGTTATGCCTTGCT
GTCAACCTTGCAGCTGATGTACACCGTGGGATACTCCTTCTCTCTTATCTCCCTCTTCCTGGCT
CTCACCCTCCTCTTGTTTCTTCGAAAACTCCACTGCACGCGCAACTACATCCACATGAACTTGT
TTGCTTCTTTCATCCTGAGAACCCTGGCTGTACTGGTGAAGGACGTCGTCTTCTACAACTCTTA
CTCCAAGAGGCCTGACAATGAGAATGGGTGGATGTCCTACCTGTCAGAGATGTCCACCTCCTGC
CGCTCAGTCCAGGTTCTCTTGCATTACTTTGTGGGTGCCAATTACTTATGGCTGCTGGTTGAAG
GCCTCTACCTCCACACGCTGCTGGAGCCCACAGTGCTTCCTGAGAGGCGGCTGTGGCCCAGATA
CCTGCTGTTGGGTTGGGCCTTCCCTGTGCTATTTGTTGTACCCTGGGGTTTCGCCCGTGCACAC
CTGGAGAACACAGGGTGCTGGACAACAAATGGGAATAAGAAAATCTGGTGGATCATCCGAGGAC
CCATGATGCTCTGTGTAACAGTCAATTTCTTCATCTTCCTGAAAATTCTCAAGCTTCTCATTTC
TAAGCTCAAAGCTCATCAAATGTGCTTCAGAGATTATAAATACAGATTGGCAAAATCAACACTG
GTCCTCATTCCTTTATTGGGCGTTCATGAGATCCTCTTCTCTTTCATCACTGATGATCAAGTTG
AAGGATTTGCAAAACTTATACGACTTTTCATTCAGTTGACACTGAGCTCCTTTCATGGGTTCCT
GGTGGCCTTGCAGTATGGTTTTGCCAATGGAGAGGTGAAGGCTGAGCTGCGGAAATACTGGGTC
CGCTTCTTGCTAGCCCGCCACTCAGGCTGCAGAGCCTGTGTCCTGGGGAAGGACTTCCGGTTCC
TAGGAAAATGTCCCAAGAAGCTCTCGGAAGGAGATGGCGCTGAGAAGCTTCGGAAGCTGCAGCC
CTCACTTAACAGTGGGCGGCTCCTACATCTAGCCATGCGAGGTCTTGGGGAGCTGGGCGCCCAG
CCCCAACAGGACCATGCACGCTGGCCCCGGGGCAGCAGCCTGTCCGAGTGCAGTGAGGGGGATG
TCACCATGGCCAACACCATGGAGGAGATTCTGGAAGAGAGTGAGATCTAGGGTGGAGTTCCACC
ACCCTGGCTCTGCTCCCAGGGACTCTTGAGGGGGCCCAGGAAGAGGAAGCAAAGCAGGACACAC
GTTGCTGGGCACGGAATCATTCTCGTTCCATTCACCATGCCACTTTGATATGAAAGCTATCACA
AGGTTCTTCAAGCTCTGTATGAAAGAGGCTGTGTGTCATGCTCACAGCCTCTGCCTGCTCTTCT
CATCCTAATAACCCCCACCAGTGTGTTTTCCACAATGCCCACCAGACCCTAGGGCCTGGCTCTA
AATTCAAGCCAATGAAGTCCCACCATGAAGAGAGGTCTCCTGTTATAGAGAAGCCAGCCAATAT
CTCTTCCTTTATCCCTTGGGGTGCATGCTTTCCATCTGAGGTTGGGTTTAGGGTGCGTGAAAAC
CTCCTAGGAAGCTTTTAAAATGCAGAATCCTAGACTTGTGGCTAAGATTCTAAGACAGTGAGTC
TGGGACCATGGCCAGGAATTGGAGCTGTTTAATAAGCATCCCAGGTAATTCTGCTGCAAGCCCA
CCCTTGGAGAACACTGGGCAGGGTGAGAGGGAGCTAGAAGCGCCCCCATGTGGCCATGGCAGGA
TGCTGCAAGAGACAGTCTGCTCTCCCAGGTCAGCTGGGGTGTGCCTGCCCTCCTTGGAGAGTAT
GTAACTCCACCCACCAGAGTGCCACTCCTCTCTGCTCTTCCTCTCCTATCAAGTCTTGCCTCTC
TCTCTCTTTGCCTCAGTTCTCTGTCCCTGCACAGCAGGAGTTCTGCTTGATCCTCCCTTTGAGG
ATTGGCCCCAGTGCCTGGGGACCCTCTGAATGTCGTCTTTGGTCTGTTCCTCTCCTTTCTGGCT
CTATCTACCTTTCTGAGTTTGGCTTCTACCAGCCTGATTTACACTACCATTCTCTTGGGGCAAG
GAATGTCCCCACCATTTTTGGTTTGCCATTGATGCATTGATTGTCACACCTGTTGTCCCAGGAA
GTTGACCTATAACTCTCCATGGCCAGAGTCCCTGCTGATCAGAATTCAATTTGCCCAGTGGGAA
TAAATACTGAAAGCAGGAGGGCCCAGGTAAAGCAATAGGAGTTTGGCTGGATCTGGACATGCCC
AGGGTGGCTCTGAGAGATCCAAGACTTTGCATCCACCAGCCTGTGGGATCTTTCCTGCCTACTG
TGACCCATGGAGGCTGAGGAGGGCCCAGGCAGTTGGGGTCAGGCTCAATGACTGAAAGTATAGG
GCAAGAGGCTGTAGGAAGATCAAGGGATGGACATCCTTTGGAAACAGTGTGTTAATGCACAGGA
GTGTCACTTTCATGGTATGTAAAATGCATGTGTACGTGGGTGGGGTATGTTGCTATGGGACTAA
ATACCACCTTGTCTTCGGGGGAGTCAGTTTGATACTCCTCAAGCAGGGCTGCCATATTTAGCAA
ACAAAAACAAGGTACTCAATTAAATTTGAATTTCAGACAAATAGTCTTCTTGTATAAGTATATC
CCATGGGCATATTTAATCTGAGATTGGAATTCAATCATGCATCTTGTCTTTTACTGGCATCTCT
GTTTTCAAGGATACTTTGCCACAGGGCTGGGACTAGGGTGAAATAATCAAGGCACTCATCTCTA
AAAAGCTCAAAGTAAATGATCAAAATAAATCATATTTTAATGCAATATTCTAAAAAAACAAATT
AACAAACTACAGCCCATGAGCCATTTATAGAAATGAAATTTGATTGGAGCCAGGGGCAGGATAA
GGGTGAGGCAGGAGAGGCCAGCTCTTGCAAGTGCAGGCTCTGGTCCTGACTTTCAAATGTTGTC
TATGAGGGACTTTTAATGTGAATTTTTATTTTTAGACAATTGCATTAAAATGTTATTTATATTG
ACTATGGGGACTTTTGGGGCCCCCTTAAATTTTGCACTTGAAATGGGATCCCCACTTGTGTCAC
CCCATAGTCCAGCCCTGGTTTTAGGATGGGGATGGAGGCAAAGGCATCAGGCAAGTAATGAAGC
AAAGGTTTATTTTTTGGTGTCCAGATTATCCATAGCTCAGTCATGAAAATCTATGTCTTTCTAT
TTTTCTCCTTTCTGCAAATGTCCCTGCCTCGGCTCATCAGCCAATTAGCTCCTAGAAAGCTGGG
GTCATCTCGTATTCCCAGCAAGTACCCAGCACAGTGCCGGTTCAGAGCAGGTGCTCCACACACA
TTCCTGGAATGAGACAGCACAGAAATGGCTCTCGGGAGCCTCGGATGCTGCTGGGAGTAAGTGA
TCCAGGACCTTACCGCTAAGAGGAGAAACTTTTTTTCAAAGCATTTATAAATACTCCCTCCACC
CCTCACTCCACAAATGGGGTGATCAACACTTACTGCTTGCTCTTGTTCTGCTAATGATTAAAAC
AAGTTTATTTAATTTCA

hide sequence

RefSeq Acc Id:

XM_017025339 ⟹ XP_016880828

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI

Sequence:

show sequence

CAACCACCTCTCCTGCAGTCTCTGCATAAACAGGACCCAGAGGAGATTTTGCCTTTGTGGTTAG
CCTCAGCCCAGCCTGGACAAGCTTAATGCCTTAGAAAGAAATACCCTGCCTCAAAAAGACACCT
GCCTCTAAACTGGCTCGAGCCCCATCGCCTTCTGCCAGCCATTCCTCTGTAGCTCGAACCCCAG
CCTGTCTCAGCCAGCTTCGTGCATTGAGCAGAACCTTCAGGGTGGAGCCCGCTGACCGCCTTGT
TCTTTCTCCTCAGCCTGTCAAGGAAGTCCCAGAAAGCACAGCTGACTTAGGGAAGGTCTGGGAA
AAATCTCCCTGCTTTTGGGGGGGCAGGGGCGGGGGATGAGCCAGGGCCGAGAAGGAACTCTGAA
GACTCCGTAGATTGCTCTAGACCGCCTCAGACACTCTCGGCGCAGCGTGGAGAGGATTTGTGCA
AACATTTCCTCTGTGGACCAAGAGGAATGCAAGAGGAGGCTGCCTGCGGTGCATCTTGGACGGC
TAGAGAGATGTACCCCTACTTGTGAAGGTGCACGAGGAAGATGAAGCTGGGATCGAGCAGGGCA
GGGCCTGGGAGAGGAAGCGCGGGACTCCTGCCTGGCGTCCACGAGCTGCCCATGGGCATCCCTG
CCCCCTGGGGGACCAGTCCTCTCTCCTTCCACAGGAAGTGCTCTCTCTGGGCCCCTGGGAGGCC
CTTCCTCACTCTGGTCCTGCTGGTTTCCATCAAGCAAGTTACAGGATCCCTCCTTGAGGAAACG
ACTCGGAAGTGGGCTCAGTACAAACAGGCATGTCTGAGAGACTTACTCAAGGAACCTTCTGGCA
TATTTTGTAACGGGACATTTGATCAGTACGTGTGTTGGCCTCATTCTTCTCCTGGAAATGTCTC
TGTACCCTGCCCTTCATACTTACCTTGGTGGAGTGAAGAGCTTTGTTTACTTTCAGAGAGCTCA
GGAAGGGCCTACAGACACTGCTTGGCTCAGGGGACTTGGCAGACGATAGAGAACGCCACGGATA
TTTGGCAGGATGACTCCGAATGCTCCGAGAACCACAGCTTCAAGCAAAACGTGGATCGTTATGC
CTTGCTGTCAACCTTGCAGCTGATGTACACCGTGGGATACTCCTTCTCTCTTATCTCCCTCTTC
CTGGCTCTCACCCTCCTCTTGTTTCTTCGAAAACTCCACTGCACGCGCAACTACATCCACATGA
ACTTGTTTGCTTCTTTCATCCTGAGAACCCTGGCTGTACTGGTGAAGGACGTCGTCTTCTACAA
CTCTTACTCCAAGAGGCCTGACAATGAGAATGGGTGGATGTCCTACCTGTCAGAGATGTCCACC
TCCTGCCGCTCAGTCCAGGTTCTCTTGCATTACTTTGTGGGTGCCAATTACTTATGGCTGCTGG
TTGAAGGCCTCTACCTCCACACGCTGCTGGAGCCCACAGTGCTTCCTGAGAGGCGGCTGTGGCC
CAGATACCTGCTGTTGGGTTGGGCCTTCCCTGTGCTATTTGTTGTACCCTGGGGTTTCGCCCGT
GCACACCTGGAGAACACAGGGTGCTGGACAACAAATGGGAATAAGAAAATCTGGTGGATCATCC
GAGGACCCATGATGCTCTGTGTAACAGTCAATTTCTTCATCTTCCTGAAAATTCTCAAGCTTCT
CATTTCTAAGCTCAAAGCTCATCAAATGTGCTTCAGAGATTATAAATACAGATTGGCAAAATCA
ACACTGGTCCTCATTCCTTTATTGGGCGTTCATGAGATCCTCTTCTCTTTCATCACTGATGATC
AAGTTGAAGGATTTGCAAAACTTATACGACTTTTCATTCAGTTGACACTGAGCTCCTTTCATGG
GTTCCTGGTGGCCTTGCAGTATGGTTTTGCCAATGGAGAGGTGAAGGCTGAGCTGCGGAAATAC
TGGGTCCGCTTCTTGCTAGCCCGCCACTCAGGCTGCAGAGCCTGTGTCCTGGGGAAGGACTTCC
GGTTCCTAGGAAAATGTCCCAAGAAGCTCTCGGAAGGAGATGGCGCTGAGAAGCTTCGGAAGCT
GCAGCCCTCACTTAACAGTGGGCGGCTCCTACATCTAGCCATGCGAGGTCTTGGGGAGCTGGGC
GCCCAGCCCCAACAGGACCATGCACGCTGGCCCCGGGGCAGCAGCCTGTCCGAGTGCAGTGAGG
GGGATGTCACCATGGCCAACACCATGGAGGAGATTCTGGAAGAGAGTGAGATCTAGGGTGGAGT
TCCACCACCCTGGCTCTGCTCCCAGGGACTCTTGAGGGGGCCCAGGAAGAGGAAGCAAAGCAGG
ACACACGTTGCTGGGCACGGAATCATTCTCGTTCCATTCACCATGCCACTTTGATATGAAAGCT
ATCACAAGGTTCTTCAAGCTCTGTATGAAAGAGGCTGTGTGTCATGCTCACAGCCTCTGCCTGC
TCTTCTCATCCTAATAACCCCCACCAGTGTGTTTTCCACAATGCCCACCAGACCCTAGGGCCTG
GCTCTAAATTCAAGCCAATGAAGTCCCACCATGAAGAGAGGTCTCCTGTTATAGAGAAGCCAGC
CAATATCTCTTCCTTTATCCCTTGGGGTGCATGCTTTCCATCTGAGGTTGGGTTTAGGGTGCGT
GAAAACCTCCTAGGAAGCTTTTAAAATGCAGAATCCTAGACTTGTGGCTAAGATTCTAAGACAG
TGAGTCTGGGACCATGGCCAGGAATTGGAGCTGTTTAATAAGCATCCCAGGTAATTCTGCTGCA
AGCCCACCCTTGGAGAACACTGGGCAGGGTGAGAGGGAGCTAGAAGCGCCCCCATGTGGCCATG
GCAGGATGCTGCAAGAGACAGTCTGCTCTCCCAGGTCAGCTGGGGTGTGCCTGCCCTCCTTGGA
GAGTATGTAACTCCACCCACCAGAGTGCCACTCCTCTCTGCTCTTCCTCTCCTATCAAGTCTTG
CCTCTCTCTCTCTTTGCCTCAGTTCTCTGTCCCTGCACAGCAGGAGTTCTGCTTGATCCTCCCT
TTGAGGATTGGCCCCAGTGCCTGGGGACCCTCTGAATGTCGTCTTTGGTCTGTTCCTCTCCTTT
CTGGCTCTATCTACCTTTCTGAGTTTGGCTTCTACCAGCCTGATTTACACTACCATTCTCTTGG
GGCAAGGAATGTCCCCACCATTTTTGGTTTGCCATTGATGCATTGATTGTCACACCTGTTGTCC
CAGGAAGTTGACCTATAACTCTCCATGGCCAGAGTCCCTGCTGATCAGAATTCAATTTGCCCAG
TGGGAATAAATACTGAAAGCAGGAGGGCCCAGGTAAAGCAATAGGAGTTTGGCTGGATCTGGAC
ATGCCCAGGGTGGCTCTGAGAGATCCAAGACTTTGCATCCACCAGCCTGTGGGATCTTTCCTGC
CTACTGTGACCCATGGAGGCTGAGGAGGGCCCAGGCAGTTGGGGTCAGGCTCAATGACTGAAAG
TATAGGGCAAGAGGCTGTAGGAAGATCAAGGGATGGACATCCTTTGGAAACAGTGTGTTAATGC
ACAGGAGTGTCACTTTCATGGTATGTAAAATGCATGTGTACGTGGGTGGGGTATGTTGCTATGG
GACTAAATACCACCTTGTCTTCGGGGGAGTCAGTTTGATACTCCTCAAGCAGGGCTGCCATATT
TAGCAAACAAAAACAAGGTACTCAATTAAATTTGAATTTCAGACAAATAGTCTTCTTGTATAAG
TATATCCCATGGGCATATTTAATCTGAGATTGGAATTCAATCATGCATCTTGTCTTTTACTGGC
ATCTCTGTTTTCAAGGATACTTTGCCACAGGGCTGGGACTAGGGTGAAATAATCAAGGCACTCA
TCTCTAAAAAGCTCAAAGTAAATGATCAAAATAAATCATATTTTAATGCAATATTCTAAAAAAA
CAAATTAACAAACTACAGCCCATGAGCCATTTATAGAAATGAAATTTGATTGGAGCCAGGGGCA
GGATAAGGGTGAGGCAGGAGAGGCCAGCTCTTGCAAGTGCAGGCTCTGGTCCTGACTTTCAAAT
GTTGTCTATGAGGGACTTTTAATGTGAATTTTTATTTTTAGACAATTGCATTAAAATGTTATTT
ATATTGACTATGGGGACTTTTGGGGCCCCCTTAAATTTTGCACTTGAAATGGGATCCCCACTTG
TGTCACCCCATAGTCCAGCCCTGGTTTTAGGATGGGGATGGAGGCAAAGGCATCAGGCAAGTAA
TGAAGCAAAGGTTTATTTTTTGGTGTCCAGATTATCCATAGCTCAGTCATGAAAATCTATGTCT
TTCTATTTTTCTCCTTTCTGCAAATGTCCCTGCCTCGGCTCATCAGCCAATTAGCTCCTAGAAA
GCTGGGGTCATCTCGTATTCCCAGCAAGTACCCAGCACAGTGCCGGTTCAGAGCAGGTGCTCCA
CACACATTCCTGGAATGAGACAGCACAGAAATGGCTCTCGGGAGCCTCGGATGCTGCTGGGAGT
AAGTGATCCAGGACCTTACCGCTAAGAGGAGAAACTTTTTTTCAAAGCATTTATAAATACTCCC
TCCACCCCTCACTCCACAAATGGGGTGATCAACACTTACTGCTTGCTCTTGTTCTGCTAATGAT
TAAAACAAGTTTATTTAATTTCA

hide sequence

RefSeq Acc Id:

XM_017025340 ⟹ XP_016880829

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI

Sequence:

show sequence

TGAGCAACCACCTCTCCTGCAGTCTCTGCATAAACAGGACCCAGAGGAGATTTTGCCTTTGTGG
TTAGCCTCAGCCCAGCCTGGACAAGCTTAATGCCTTAGAAAGAAATACCCTGCCTCAAAAAGAC
ACCTGCCTCTAAACTGGCTCGAGCCCCATCGCCTTCTGCCAGCCATTCCTCTGTAGCTCGAACC
CCAGCCTGTCTCAGCCAGCTTCGTGCATTGAGCAGAACCTTCAGGGTGGAGCCCGCTGACCGCC
TTGTTCTTTCTCCTCAGCCTGTCAAGGAAGTCCCAGAAAGCACAGCTGACTTAGGGAAGGTCTG
GGAAAAATCTCCCTGCTTTTGGGGGGGCAGGGGCGGGGGATGAGCCAGGGCCGAGAAGGAACTC
TGAAGACTCCGTAGATTGCTCTAGACCGCCTCAGACACTCTCGGCGCAGCGTGGAGAGGATTTG
TGCAAACATTTCCTCTGTGGACCAAGAGGAATGCAAGAGGAGGCTGCCTGCGGTGCATCTTGGA
CGGCTAGAGAGATGTACCCCTACTTGTGAAGGTGCACGAGGAAGATGAAGCTGGGATCGAGCAG
GGCAGGGCCTGGGAGAGGAAGCGCGGGACTCCTGCCTGGCGTCCACGAGCTGCCCATGGGCATC
CCTGCCCCCTGGGGGACCAGTCCTCTCTCCTTCCACAGGAAGTGCTCTCTCTGGGCCCCTGGGA
GGCCCTTCCTCACTCTGGTCCTGCTGGTTTCCATCAAGCAAGCATATTTTGTAACGGGACATTT
GATCAGTACGTGTGTTGGCCTCATTCTTCTCCTGGAAATGTCTCTGTACCCTGCCCTTCATACT
TACCTTGGTGGAGTGAAGGTGGATCGTTATGCCTTGCTGTCAACCTTGCAGCTGATGTACACCG
TGGGATACTCCTTCTCTCTTATCTCCCTCTTCCTGGCTCTCACCCTCCTCTTGTTTCTTCGAAA
ACTCCACTGCACGCGCAACTACATCCACATGAACTTGTTTGCTTCTTTCATCCTGAGAACCCTG
GCTGTACTGGTGAAGGACGTCGTCTTCTACAACTCTTACTCCAAGAGGCCTGACAATGAGAATG
GGTGGATGTCCTACCTGTCAGAGATGTCCACCTCCTGCCGCTCAGTCCAGGTTCTCTTGCATTA
CTTTGTGGGTGCCAATTACTTATGGCTGCTGGTTGAAGGCCTCTACCTCCACACGCTGCTGGAG
CCCACAGTGCTTCCTGAGAGGCGGCTGTGGCCCAGATACCTGCTGTTGGGTTGGGCCTTCCCTG
TGCTATTTGTTGTACCCTGGGGTTTCGCCCGTGCACACCTGGAGAACACAGGGTGCTGGACAAC
AAATGGGAATAAGAAAATCTGGTGGATCATCCGAGGACCCATGATGCTCTGTGTAACAGTCAAT
TTCTTCATCTTCCTGAAAATTCTCAAGCTTCTCATTTCTAAGCTCAAAGCTCATCAAATGTGCT
TCAGAGATTATAAATACAGATTGGCAAAATCAACACTGGTCCTCATTCCTTTATTGGGCGTTCA
TGAGATCCTCTTCTCTTTCATCACTGATGATCAAGTTGAAGGATTTGCAAAACTTATACGACTT
TTCATTCAGTTGACACTGAGCTCCTTTCATGGGTTCCTGGTGGCCTTGCAGTATGGTTTTGCCA
ATGGAGAGGTGAAGGCTGAGCTGCGGAAATACTGGGTCCGCTTCTTGCTAGCCCGCCACTCAGG
CTGCAGAGCCTGTGTCCTGGGGAAGGACTTCCGGTTCCTAGGAAAATGTCCCAAGAAGCTCTCG
GAAGGAGATGGCGCTGAGAAGCTTCGGAAGCTGCAGCCCTCACTTAACAGTGGGCGGCTCCTAC
ATCTAGCCATGCGAGGTCTTGGGGAGCTGGGCGCCCAGCCCCAACAGGACCATGCACGCTGGCC
CCGGGGCAGCAGCCTGTCCGAGTGCAGTGAGGGGGATGTCACCATGGCCAACACCATGGAGGAG
ATTCTGGAAGAGAGTGAGATCTAGGGTGGAGTTCCACCACCCTGGCTCTGCTCCCAGGGACTCT
TGAGGGGGCCCAGGAAGAGGAAGCAAAGCAGGACACACGTTGCTGGGCACGGAATCATTCTCGT
TCCATTCACCATGCCACTTTGATATGAAAGCTATCACAAGGTTCTTCAAGCTCTGTATGAAAGA
GGCTGTGTGTCATGCTCACAGCCTCTGCCTGCTCTTCTCATCCTAATAACCCCCACCAGTGTGT
TTTCCACAATGCCCACCAGACCCTAGGGCCTGGCTCTAAATTCAAGCCAATGAAGTCCCACCAT
GAAGAGAGGTCTCCTGTTATAGAGAAGCCAGCCAATATCTCTTCCTTTATCCCTTGGGGTGCAT
GCTTTCCATCTGAGGTTGGGTTTAGGGTGCGTGAAAACCTCCTAGGAAGCTTTTAAAATGCAGA
ATCCTAGACTTGTGGCTAAGATTCTAAGACAGTGAGTCTGGGACCATGGCCAGGAATTGGAGCT
GTTTAATAAGCATCCCAGGTAATTCTGCTGCAAGCCCACCCTTGGAGAACACTGGGCAGGGTGA
GAGGGAGCTAGAAGCGCCCCCATGTGGCCATGGCAGGATGCTGCAAGAGACAGTCTGCTCTCCC
AGGTCAGCTGGGGTGTGCCTGCCCTCCTTGGAGAGTATGTAACTCCACCCACCAGAGTGCCACT
CCTCTCTGCTCTTCCTCTCCTATCAAGTCTTGCCTCTCTCTCTCTTTGCCTCAGTTCTCTGTCC
CTGCACAGCAGGAGTTCTGCTTGATCCTCCCTTTGAGGATTGGCCCCAGTGCCTGGGGACCCTC
TGAATGTCGTCTTTGGTCTGTTCCTCTCCTTTCTGGCTCTATCTACCTTTCTGAGTTTGGCTTC
TACCAGCCTGATTTACACTACCATTCTCTTGGGGCAAGGAATGTCCCCACCATTTTTGGTTTGC
CATTGATGCATTGATTGTCACACCTGTTGTCCCAGGAAGTTGACCTATAACTCTCCATGGCCAG
AGTCCCTGCTGATCAGAATTCAATTTGCCCAGTGGGAATAAATACTGAAAGCAGGAGGGCCCAG
GTAAAGCAATAGGAGTTTGGCTGGATCTGGACATGCCCAGGGTGGCTCTGAGAGATCCAAGACT
TTGCATCCACCAGCCTGTGGGATCTTTCCTGCCTACTGTGACCCATGGAGGCTGAGGAGGGCCC
AGGCAGTTGGGGTCAGGCTCAATGACTGAAAGTATAGGGCAAGAGGCTGTAGGAAGATCAAGGG
ATGGACATCCTTTGGAAACAGTGTGTTAATGCACAGGAGTGTCACTTTCATGGTATGTAAAATG
CATGTGTACGTGGGTGGGGTATGTTGCTATGGGACTAAATACCACCTTGTCTTCGGGGGAGTCA
GTTTGATACTCCTCAAGCAGGGCTGCCATATTTAGCAAACAAAAACAAGGTACTCAATTAAATT
TGAATTTCAGACAAATAGTCTTCTTGTATAAGTATATCCCATGGGCATATTTAATCTGAGATTG
GAATTCAATCATGCATCTTGTCTTTTACTGGCATCTCTGTTTTCAAGGATACTTTGCCACAGGG
CTGGGACTAGGGTGAAATAATCAAGGCACTCATCTCTAAAAAGCTCAAAGTAAATGATCAAAAT
AAATCATATTTTAATGCAATATTCTAAAAAAACAAATTAACAAACTACAGCCCATGAGCCATTT
ATAGAAATGAAATTTGATTGGAGCCAGGGGCAGGATAAGGGTGAGGCAGGAGAGGCCAGCTCTT
GCAAGTGCAGGCTCTGGTCCTGACTTTCAAATGTTGTCTATGAGGGACTTTTAATGTGAATTTT
TATTTTTAGACAATTGCATTAAAATGTTATTTATATTGACTATGGGGACTTTTGGGGCCCCCTT
AAATTTTGCACTTGAAATGGGATCCCCACTTGTGTCACCCCATAGTCCAGCCCTGGTTTTAGGA
TGGGGATGGAGGCAAAGGCATCAGGCAAGTAATGAAGCAAAGGTTTATTTTTTGGTGTCCAGAT
TATCCATAGCTCAGTCATGAAAATCTATGTCTTTCTATTTTTCTCCTTTCTGCAAATGTCCCTG
CCTCGGCTCATCAGCCAATTAGCTCCTAGAAAGCTGGGGTCATCTCGTATTCCCAGCAAGTACC
CAGCACAGTGCCGGTTCAGAGCAGGTGCTCCACACACATTCCTGGAATGAGACAGCACAGAAAT
GGCTCTCGGGAGCCTCGGATGCTGCTGGGAGTAAGTGATCCAGGACCTTACCGCTAAGAGGAGA
AACTTTTTTTCAAAGCATTTATAAATACTCCCTCCACCCCTCACTCCACAAATGGGGTGATCAA
CACTTACTGCTTGCTCTTGTTCTGCTAATGATTAAAACAAGTTTATTTAATTTCATTTGCATTT
TGTTGATTCTTTTACATTTGTCTCTCACTGGAGCTGAAGGTCTCTCCCACCCATGAAGAATGCG
ATGCACTATTCCTGGCCAGAAGTGAGGAAAAGGGCTGTGGCGTTTAGCCAGGGACCTGGGTGCT
CCAATATCTTAAATTTGGTCTTAGGGACCAGAGGAGTGGGCAGAGGGGCCGGGACCAGAAGCAG
AGGTCAGAGGTCAAAAGAATGGAAGGAGAGTGTCTCCCCTTTTATAGACCACCCCATTGGTCAC
TCAGCTTGCCTGTTGCTTTGAAGATCTAGTCTAGTGGTTCTCAATCCTCGCATTACAATCCCTT
GGGAAGCTTTTTATTTATTTTTATTTATATTTATTTATTTGAGACCCAGTCTCACTCTGTTTCC
CAGGCTGGAGTGCAGTTGCATGATCTCAACTCACTGCAACCTCCACCTCCCGGGTTCAAGCAAT
TCTCATGCTTTAGCCTCCCGAGGAGCTGGGTCTACAGGCGTGAGCCACCAGGCCCAGCTAATTT
TTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGAC
CTCAGGTGATTGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAAGTGTGAGCCACCACGCCC
AGCCCCCTGGGAAGCTTTTTTAAAAGACCAGTGACAGGGTCTGACCCCAGAGGTTCTGATTGAA
ATGGTCTTACTAGACCTGGGCATTGGGATTTTTATAAGTTCCTGAGTGATCTTTTTTAAATTGT
GGCAAAATATATATAACATAAAATTAACCATTGTAGCCATCTTTTTTTCTTTTTGTTTTTTGAG
ACAGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGCTGTGATCTCGGCTCACCGCAACCTCC
ACCTCCCAGGTTCAGGCAATTCTTCTGCCTCTGCCTCCCGAGTAGCTGGGACTACAGGCGCCTG
CCACCACTCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGTCAGGCT
GGTCTCAAACTCCTGACCCCAGGTGATCCACGCGCCTTGGCCTCCCAAAGTGCTGGGATTACAG
GCGTGAGCCACCGCGCCCGGCCAGCCATTATTAAGTGTATGGTTCAGTGGCATGAAGTACCTTC
TTACTGTTGTGCAGCCGTCACCACCATCCATCTCCAGGACTCTTTCATCTTCCTGAACTGAAAC
TCTACATCCATTAAACAATAGCCTCCCATTCTTTCCTCCCCAAGCCCCTGACAACTTCTACTTC
CTGTCTCTGTGAATTTGCTTATTCTGGATACATCAGCTATAAGTGGAACTGTATAGTATGTATC
CTTTTGTGATCAGCTTATTTCACTCCCATAGTGCCCTCAAGGATCATCCACCTTGTAGTGTGTG
TCAGAAATTCCTTTTTTAAAATGCTGAATAATATTCCATGCATACCACATTTTGTTTATCTGTT
CATCCATTGATGGACACTTGGCTTGTTTCCATGTTTGGCTATTGTGAATAATGCTGCTATTGGT
AGGGATGTATAAACATCTGGTTTCTGTTTTAAAAATTTGAGTATACCTACAAGTGGAACTGCTG
AATCATATGGTGATTCTATATTTTCCCCAACAGCTGCGCCATTTTATATTCCCACCAGCAATGC
ATGAGGATTCCAAATGCTCCATGGCCTTTGCCAACATTTATTTTCTATTTTTTTATGATAACCA
TTCCTAATGGCTGTGAAATGGTATCTCATTGTGGTTTTGATTTGCGTTTCCGGAATGACTAATG
ATGTCAAGCATCTTTTTATGTGCCTGCTGATTAGTCCTTTGTGAGTCTTCTTTAGAAAAATATC
TATTCAATTCTTGGCCCATTTTTCAATTGGATTGTTTGTTTTTTGTTGTTGAGTTGCAGGAATT
CTTTATGCATTCTGAATATGGATACCTTATCTATTATTTGCAAATATTTTCTCTCATTCTGTAG
ATTGTCTTTTTGCCTCTTGATAGTGCCCTTTTATGTAGAAAAGTTTTAAATTTTGTTGAAGTCC
AA

hide sequence

RefSeq Acc Id:

XM_017025341 ⟹ XP_016880830

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,892,099 (+)	NCBI

Sequence:

show sequence

AGCAACCACCTCTCCTGCAGTCTCTGCATAAACAGGACCCAGAGGAGATTTTGCCTTTGTGGTT
AGCCTCAGCCCAGCCTGGACAAGCTTAATGCCTTAGAAAGAAATACCCTGCCTCAAAAAGACAC
CTGCCTCTAAACTGGCTCGAGCCCCATCGCCTTCTGCCAGCCATTCCTCTGTAGCTCGAACCCC
AGCCTGTCTCAGCCAGCTTCGTGCATTGAGCAGAACCTTCAGGGTGGAGCCCGCTGACCGCCTT
GTTCTTTCTCCTCAGCCTGTCAAGGAAGTCCCAGAAAGCACAGCTGACTTAGGGAAGGTCTGGG
AAAAATCTCCCTGCTTTTGGGGGGGCAGGGGCGGGGGATGAGCCAGGGCCGAGAAGGAACTCTG
AAGACTCCGTAGATTGCTCTAGACCGCCTCAGACACTCTCGGCGCAGCGTGGAGAGGATTTGTG
CAAACATTTCCTCTGTGGACCAAGAGGAATGCAAGAGGAGGCTGCCTGCGGTGCATCTTGGACG
GCTAGAGAGATGTACCCCTACTTGTGAAGGTGCACGAGGAAGATGAAGCTGGGATCGAGCAGGG
CAGGGCCTGGGAGAGGAAGCGCGGGACTCCTGCCTGGCGTCCACGAGCTGCCCATGGGCATCCC
TGCCCCCTGGGGGACCAGTCCTCTCTCCTTCCACAGGAAGTGCTCTCTCTGGGCCCCTGGGAGG
CCCTTCCTCACTCTGGTCCTGCTGGTTTCCATCAAGCAAGTGGATCGTTATGCCTTGCTGTCAA
CCTTGCAGCTGATGTACACCGTGGGATACTCCTTCTCTCTTATCTCCCTCTTCCTGGCTCTCAC
CCTCCTCTTGTTTCTTCGAAAACTCCACTGCACGCGCAACTACATCCACATGAACTTGTTTGCT
TCTTTCATCCTGAGAACCCTGGCTGTACTGGTGAAGGACGTCGTCTTCTACAACTCTTACTCCA
AGAGGCCTGACAATGAGAATGGGTGGATGTCCTACCTGTCAGAGATGTCCACCTCCTGCCGCTC
AGTCCAGGTTCTCTTGCATTACTTTGTGGGTGCCAATTACTTATGGCTGCTGGTTGAAGGCCTC
TACCTCCACACGCTGCTGGAGCCCACAGTGCTTCCTGAGAGGCGGCTGTGGCCCAGATACCTGC
TGTTGGGTTGGGCCTTCCCTGTGCTATTTGTTGTACCCTGGGGTTTCGCCCGTGCACACCTGGA
GAACACAGGGTGCTGGACAACAAATGGGAATAAGAAAATCTGGTGGATCATCCGAGGACCCATG
ATGCTCTGTGTAACAGTCAATTTCTTCATCTTCCTGAAAATTCTCAAGCTTCTCATTTCTAAGC
TCAAAGCTCATCAAATGTGCTTCAGAGATTATAAATACAGATTGGCAAAATCAACACTGGTCCT
CATTCCTTTATTGGGCGTTCATGAGATCCTCTTCTCTTTCATCACTGATGATCAAGTTGAAGGA
TTTGCAAAACTTATACGACTTTTCATTCAGTTGACACTGAGCTCCTTTCATGGGTTCCTGGTGG
CCTTGCAGTATGGTTTTGCCAATGGAGAGGTGAAGGCTGAGCTGCGGAAATACTGGGTCCGCTT
CTTGCTAGCCCGCCACTCAGGCTGCAGAGCCTGTGTCCTGGGGAAGGACTTCCGGTTCCTAGGA
AAATGTCCCAAGAAGCTCTCGGAAGGAGATGGCGCTGAGAAGCTTCGGAAGCTGCAGCCCTCAC
TTAACAGTGGGCGGCTCCTACATCTAGCCATGCGAGGTCTTGGGGAGCTGGGCGCCCAGCCCCA
ACAGGACCATGCACGCTGGCCCCGGGGCAGCAGCCTGTCCGAGTGCAGTGAGGGGGATGTCACC
ATGGCCAACACCATGGAGGAGATTCTGGAAGAGAGTGAGATCTAGGGTGGAGTTCCACCACCCT
GGCTCTGCTCCCAGGGACTCTTGAGGGGGCCCAGGAAGAGGAAGCAAAGCAGGACACACGTTGC
TGGGCACGGAATCATTCTCGTTCCATTCACCATGCCACTTTGATATGAAAGCTATCACAAGGTT
CTTCAAGCTCTGTATGAAAGAGGCTGTGTGTCATGCTCACAGCCTCTGCCTGCTCTTCTCATCC
TAATAACCCCCACCAGTGTGTTTTCCACAATGCCCACCAGACCCTAGGGCCTGGCTCTAAATTC
AAGCCAATGAAGTCCCACCATGAAGAGAGGTCTCCTGTTATAGAGAAGCCAGCCAATATCTCTT
CCTTTATCCCTTGGGGTGCATGCTTTCCATCTGAGGTTGGGTTTAGGGTGCGTGAAAACCTCCT
AGGAAGCTTTTAAAATGCAGAATCCTAGACTTGTGGCTAAGATTCTAAGACAGTGAGTCTGGGA
CCATGGCCAGGAATTGGAGCTGTTTAATAAGCATCCCAGGTAATTCTGCTGCAAGCCCACCCTT
GGAGAACACTGGGCAGGGTGAGAGGGAGCTAGAAGCGCCCCCATGTGGCCATGGCAGGATGCTG
CAAGAGACAGTCTGCTCTCCCAGGTCAGCTGGGGTGTGCCTGCCCTCCTTGGAGAGTATGTAAC
TCCACCCACCAGAGTGCCACTCCTCTCTGCTCTTCCTCTCCTATCAAGTCTTGCCTCTCTCTCT
CTTTGCCTCAGTTCTCTGTCCCTGCACAGCAGGAGTTCTGCTTGATCCTCCCTTTGAGGATTGG
CCCCAGTGCCTGGGGACCCTCTGAATGTCGTCTTTGGTCTGTTCCTCTCCTTTCTGGCTCTATC
TACCTTTCTGAGTTTGGCTTCTACCAGCCTGATTTACACTACCATTCTCTTGGGGCAAGGAATG
TCCCCACCATTTTTGGTTTGCCATTGATGCATTGATTGTCACACCTGTTGTCCCAGGAAGTTGA
CCTATAACTCTCCATGGCCAGAGTCCCTGCTGATCAGAATTCAATTTGCCCAGTGGGAATAAAT
ACTGAAAGCAGGAGGGCCCAGGTAAAGCAATAGGAGTTTGGCTGGATCTGGACATGCCCAGGGT
GGCTCTGAGAGATCCAAGACTTTGCATCCACCAGCCTGTGGGATCTTTCCTGCCTACTGTGACC
CATGGAGGCTGAGGAGGGCCCAGGCAGTTGGGGTCAGGCTCAATGACTGAAAGTATAGGGCAAG
AGGCTGTAGGAAGATCAAGGGATGGACATCCTTTGGAAACAGTGTGTTAATGCACAGGAGTGTC
ACTTTCATGGTATGTAAAATGCATGTGTACGTGGGTGGGGTATGTTGCTATGGGACTAAATACC
ACCTTGTCTTCGGGGGAGTCAGTTTGATACTCCTCAAGCAGGGCTGCCATATTTAGCAAACAAA
AACAAGGTACTCAATTAAATTTGAATTTCAGACAAATAGTCTTCTTGTATAAGTATATCCCATG
GGCATATTTAATCTGAGATTGGAATTCAATCATGCATCTTGTCTTTTACTGGCATCTCTGTTTT
CAAGGATACTTTGCCACAGGGCTGGGACTAGGGTGAAATAATCAAGGCACTCATCTCTAAAAAG
CTCAAAGTAAATGATCAAAATAAATCATATTTTAATGCAATATTCTAAAAAAACAAATTAACAA
ACTACAGCCCATGAGCCATTTATAGAAATGAAATTTGATTGGAGCCAGGGGCAGGATAAGGGTG
AGGCAGGAGAGGCCAGCTCTTGCAAGTGCAGGCTCTGGTCCTGACTTTCAAATGTTGTCTATGA
GGGACTTTTAATGTGAATTTTTATTTTTAGACAATTGCATTAAAATGTTATTTATATTGACTAT
GGGGACTTTTGGGGCCCCCTTAAATTTTGCACTTGAAATGGGATCCCCACTTGTGTCACCCCAT
AGTCCAGCCCTGGTTTTAGGATGGGGATGGAGGCAAAGGCATCAGGCAAGTAATGAAGCAAAGG
TTTATTTTTTGGTGTCCAGATTATCCATAGCTCAGTCATGAAAATCTATGTCTTTCTATTTTTC
TCCTTTCTGCAAATGTCCCTGCCTCGGCTCATCAGCCAATTAGCTCCTAGAAAGCTGGGGTCAT
CTCGTATTCCCAGCAAGTACCCAGCACAGTGCCGGTTCAGAGCAGGTGCTCCACACACATTCCT
GGAATGAGACAGCACAGAAATGGCTCTCGGGAGCCTCGGATGCTGCTGGGAGTAAGTGATCCAG
GACCTTACCGCTAAGAGGAGAAACTTTTTTTCAAAGCATTTATAAATACTCCCTCCACCCCTCA
CTCCACAAATGGGGTGATCAACACTTACTGCTTGCTCTTGTTCTGCTAATGATTAAAACAAGTT
TATTTAATTTCATTTGCATTTTGTTGATTCTTTTACATTTGTCTCTCACTGGAGCTGAAGGTCT
CTCCCACCCATGAAGAATGCGATGCACTATTCCTGGCCAGAAGTGAGGAAAAGGGCTGTGGCGT
TTAGCCAGGGACCTGGGTGCTCCAATATCTTAAATTTGGTCTTAGGGACCAGAGGAGTGGGCAG
AGGGGCCGGGACCAGAAGCAGAGGTCAGAGGTCAAAAGAATGGAAGGAGAGTGTCTCCCCTTTT
ATAGACCACCCCATTGGTCACTCAGCTTGCCTGTTGCTTTGAAGATCTAGTCTAGTGGTTCTCA
ATCCTCGCATTACAATCCCTTGGGAAGCTTTTTATTTATTTTTATTTATATTTATTTATTTGAG
ACCCAGTCTCACTCTGTTTCCCAGGCTGGAGTGCAGTTGCATGATCTCAACTCACTGCAACCTC
CACCTCCCGGGTTCAAGCAATTCTCATGCTTTAGCCTCCCGAGGAGCTGGGTCTACAGGCGTGA
GCCACCAGGCCCAGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCA
GGCTGGTCTTGAACTCCTGACCTCAGGTGATTGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTA
CAAGTGTGAGCCACCACGCCCAGCCCCCTGGGAAGCTTTTTTAAAAGACCAGTGACAGGGTCTG
ACCCCAGAGGTTCTGATTGAAATGGTCTTACTAGACCTGGGCATTGGGATTTTTATAAGTTCCT
GAGTGATCTTTTTTAAATTGTGGCAAAATATATATAACATAAAATTAACCATTGTAGCCATCTT
TTTTTCTTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGCTGTGA
TCTCGGCTCACCGCAACCTCCACCTCCCAGGTTCAGGCAATTCTTCTGCCTCTGCCTCCCGAGT
AGCTGGGACTACAGGCGCCTGCCACCACTCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGG
TTTCACCATATTGGTCAGGCTGGTCTCAAACTCCTGACCCCAGGTGATCCACGCGCCTTGGCCT
CCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCAGCCATTATTAAGTGTATGGT
TCAGTGGCATGAAGTACCTTCTTACTGTTGTGCAGCCGTCACCACCATCCATCTCCAGGACTCT
TTCATCTTCCTGAACTGAAACTCTACATCCATTAAACAATAGCCTCCCATTCTTTCCTCCCCAA
GCCCCTGACAACTTCTACTTCCTGTCTCTGTGAATTTGCTTATTCTGGATACATCAGCTATAAG
TGGAACTGTATAGTATGTATCCTTTTGTGATCAGCTTATTTCACTCCCATAGTGCCCTCAAGGA
TCATCCACCTTGTAGTGTGTGTCAGAAATTCCTTTTTTAAAATGCTGAATAATATTCCATGCAT
ACCACATTTTGTTTATCTGTTCATCCATTGATGGACACTTGGCTTGTTTCCATGTTTGGCTATT
GTGAATAATGCTGCTATTGGTAGGGATGTATAAACATCTGGTTTCTGTTTTAAAAATTTGAGTA
TACCTACAAGTGGAACTGCTGAATCATATGGTGATTCTATATTTTCCCCAACAGCTGCGCCATT
TTATATTCCCACCAGCAATGCATGAGGATTCCAAATGCTCCATGGCCTTTGCCAACATTTATTT
TCTATTTTTTTATGATAACCATTCCTAATGGCTGTGAAATGGTATCTCATTGTGGTTTTGATTT
GCGTTTCCGGAATGACTAATGATGTCAAGCATCTTTTTATGTGCCTGCTGATTAGTCCTTTGTG
AGTCTTCTTTAGAAAAATATCTATTCAATTCTTGGCCCATTTTTCAATTGGATTGTTTGTTTTT
TGTTGTTGAGTTGCAGGAATTCTTTATGCATTCTGAATATGGATACCTTATCTATTATTTGCAA
ATATTTTCTCTCATTCTGTAGATTGTCTTTTTGCCTCTTGATAGTGCCCTTTTATGTAGAAAAG
TTTTAAATTTTGTTGAAGTCCAA

hide sequence

RefSeq Acc Id:

XM_054317814 ⟹ XP_054173789

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI

RefSeq Acc Id:

XM_054317815 ⟹ XP_054173790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI

RefSeq Acc Id:

XM_054317816 ⟹ XP_054173791

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI

RefSeq Acc Id:

XM_054317817 ⟹ XP_054173792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	9,733,669 - 9,799,834 (+)	NCBI

RefSeq Acc Id:

XM_054317818 ⟹ XP_054173793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	9,741,552 - 9,799,834 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_004237	(Get FASTA)	NCBI Sequence Viewer
	XP_011522379	(Get FASTA)	NCBI Sequence Viewer
	XP_016880828	(Get FASTA)	NCBI Sequence Viewer
	XP_016880829	(Get FASTA)	NCBI Sequence Viewer
	XP_016880830	(Get FASTA)	NCBI Sequence Viewer
	XP_054173789	(Get FASTA)	NCBI Sequence Viewer
	XP_054173790	(Get FASTA)	NCBI Sequence Viewer
	XP_054173791	(Get FASTA)	NCBI Sequence Viewer
	XP_054173792	(Get FASTA)	NCBI Sequence Viewer
	XP_054173793	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD16895	(Get FASTA)	NCBI Sequence Viewer
	AAH19818	(Get FASTA)	NCBI Sequence Viewer
	AAH41176	(Get FASTA)	NCBI Sequence Viewer
	AAH43390	(Get FASTA)	NCBI Sequence Viewer
	AAH96261	(Get FASTA)	NCBI Sequence Viewer
	AAH96262	(Get FASTA)	NCBI Sequence Viewer
	AAH96263	(Get FASTA)	NCBI Sequence Viewer
	AAH96264	(Get FASTA)	NCBI Sequence Viewer
	ADO22360	(Get FASTA)	NCBI Sequence Viewer
	BAG36931	(Get FASTA)	NCBI Sequence Viewer
	BAG58590	(Get FASTA)	NCBI Sequence Viewer
	EAW90015	(Get FASTA)	NCBI Sequence Viewer
	EAW90016	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000262441
	ENSP00000262441.5
	ENSP00000303605.5
	ENSP00000404471.3
	ENSP00000458242
	ENSP00000458242.1
GenBank Protein	O95838	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_004237 ⟸ NM_004246

- UniProtKB:

Q4VAT3 (UniProtKB/Swiss-Prot), O95838 (UniProtKB/Swiss-Prot), B2RAN4 (UniProtKB/TrEMBL), A0A384MTS7 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVSIKQV
TGSLLEETTRKWAQYKQACLRDLLKEPSGIFCNGTFDQYVCWPHSSPGNVSVPCPSYLPWWSEE
SSGRAYRHCLAQGTWQTIENATDIWQDDSECSENHSFKQNVDRYALLSTLQLMYTVGYSFSLIS
LFLALTLLLFLRKLHCTRNYIHMNLFASFILRTLAVLVKDVVFYNSYSKRPDNENGWMSYLSEM
STSCRSVQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLPERRLWPRYLLLGWAFPVLFVVPWGF
ARAHLENTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFLKILKLLISKLKAHQMCFRDYKYRLA
KSTLVLIPLLGVHEILFSFITDDQVEGFAKLIRLFIQLTLSSFHGFLVALQYGFANGEVKAELR
KYWVRFLLARHSGCRACVLGKDFRFLGKCPKKLSEGDGAEKLRKLQPSLNSGRLLHLAMRGLGE
LGAQPQQDHARWPRGSSLSECSEGDVTMANTMEEILEESEI

hide sequence

RefSeq Acc Id:	XP_011522379 ⟸ XM_011524077
- Peptide Label:	isoform X1
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVSIKQV TGSLLEETTRKWAQYKQACLRDLLKEPSGIFCNGTFDQYVCWPHSSPGNVSVPCPSYLPWWSED HQQIQGQLKLFSGKISGYKLQAKQESSGRAYRHCLAQGTWQTIENATDIWQDDSECSENHSFKQ NVDRYALLSTLQLMYTVGYSFSLISLFLALTLLLFLRKLHCTRNYIHMNLFASFILRTLAVLVK DVVFYNSYSKRPDNENGWMSYLSEMSTSCRSVQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLP ERRLWPRYLLLGWAFPVLFVVPWGFARAHLENTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFL KILKLLISKLKAHQMCFRDYKYRLAKSTLVLIPLLGVHEILFSFITDDQVEGFAKLIRLFIQLT LSSFHGFLVALQYGFANGEVKAELRKYWVRFLLARHSGCRACVLGKDFRFLGKCPKKLSEGDGA EKLRKLQPSLNSGRLLHLAMRGLGELGAQPQQDHARWPRGSSLSECSEGDVTMANTMEEILEES EI hide sequence

RefSeq Acc Id:	XP_016880829 ⟸ XM_017025340
- Peptide Label:	isoform X3
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVSIKQA YFVTGHLISTCVGLILLLEMSLYPALHTYLGGVKVDRYALLSTLQLMYTVGYSFSLISLFLALT LLLFLRKLHCTRNYIHMNLFASFILRTLAVLVKDVVFYNSYSKRPDNENGWMSYLSEMSTSCRS VQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLPERRLWPRYLLLGWAFPVLFVVPWGFARAHLE NTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFLKILKLLISKLKAHQMCFRDYKYRLAKSTLVL IPLLGVHEILFSFITDDQVEGFAKLIRLFIQLTLSSFHGFLVALQYGFANGEVKAELRKYWVRF LLARHSGCRACVLGKDFRFLGKCPKKLSEGDGAEKLRKLQPSLNSGRLLHLAMRGLGELGAQPQ QDHARWPRGSSLSECSEGDVTMANTMEEILEESEI hide sequence

RefSeq Acc Id:	XP_016880830 ⟸ XM_017025341
- Peptide Label:	isoform X4
- UniProtKB:	I3L0P5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVSIKQV DRYALLSTLQLMYTVGYSFSLISLFLALTLLLFLRKLHCTRNYIHMNLFASFILRTLAVLVKDV VFYNSYSKRPDNENGWMSYLSEMSTSCRSVQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLPER RLWPRYLLLGWAFPVLFVVPWGFARAHLENTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFLKI LKLLISKLKAHQMCFRDYKYRLAKSTLVLIPLLGVHEILFSFITDDQVEGFAKLIRLFIQLTLS SFHGFLVALQYGFANGEVKAELRKYWVRFLLARHSGCRACVLGKDFRFLGKCPKKLSEGDGAEK LRKLQPSLNSGRLLHLAMRGLGELGAQPQQDHARWPRGSSLSECSEGDVTMANTMEEILEESEI hide sequence

RefSeq Acc Id:	XP_016880828 ⟸ XM_017025339
- Peptide Label:	isoform X2
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVSIKQV TGSLLEETTRKWAQYKQACLRDLLKEPSGIFCNGTFDQYVCWPHSSPGNVSVPCPSYLPWWSEE LCLLSESSGRAYRHCLAQGTWQTIENATDIWQDDSECSENHSFKQNVDRYALLSTLQLMYTVGY SFSLISLFLALTLLLFLRKLHCTRNYIHMNLFASFILRTLAVLVKDVVFYNSYSKRPDNENGWM SYLSEMSTSCRSVQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLPERRLWPRYLLLGWAFPVLF VVPWGFARAHLENTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFLKILKLLISKLKAHQMCFRD YKYRLAKSTLVLIPLLGVHEILFSFITDDQVEGFAKLIRLFIQLTLSSFHGFLVALQYGFANGE VKAELRKYWVRFLLARHSGCRACVLGKDFRFLGKCPKKLSEGDGAEKLRKLQPSLNSGRLLHLA MRGLGELGAQPQQDHARWPRGSSLSECSEGDVTMANTMEEILEESEI hide sequence

Ensembl Acc Id:

ENSP00000458242 ⟸ ENST00000574745

Ensembl Acc Id:

ENSP00000404471 ⟸ ENST00000458005

Ensembl Acc Id:

ENSP00000262441 ⟸ ENST00000262441

Ensembl Acc Id:

ENSP00000303605 ⟸ ENST00000304773

RefSeq Acc Id:	XP_054173789 ⟸ XM_054317814
- Peptide Label:	isoform X1
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054173790 ⟸ XM_054317815
- Peptide Label:	isoform X2
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054173791 ⟸ XM_054317816
- Peptide Label:	isoform X3
- UniProtKB:	B2RAN4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054173792 ⟸ XM_054317817
- Peptide Label:	isoform X4
- UniProtKB:	I3L0P5 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054173793 ⟸ XM_054317818
- Peptide Label:	isoform X5
- UniProtKB:	I3L0P5 (UniProtKB/TrEMBL)

Protein Domains

G-protein coupled receptors family 2 profile

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O95838-F1-model_v2	AlphaFold	O95838	1-553	view protein structure

Promoters

RGD ID:

7233989

Promoter ID:

EPDNEW_H22739

Type:

initiation region

Name:

GLP2R_1

Description:

glucagon like peptide 2 receptor

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22740

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,528 - 9,825,588	EPDNEW

RGD ID:

7233987

Promoter ID:

EPDNEW_H22740

Type:

initiation region

Name:

GLP2R_2

Description:

glucagon like peptide 2 receptor

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22739

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	9,825,924 - 9,825,984	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:4325	AgrOrtholog
COSMIC	GLP2R	COSMIC
Ensembl Genes	ENSG00000065325	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000262441	ENTREZGENE
	ENST00000262441.10	UniProtKB/Swiss-Prot
	ENST00000304773.5	UniProtKB/TrEMBL
	ENST00000458005.2	UniProtKB/TrEMBL
	ENST00000574745	ENTREZGENE
	ENST00000574745.5	UniProtKB/TrEMBL
Gene3D-CATH	4.10.1240.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Rhodopsin 7-helix transmembrane proteins	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000065325	GTEx
HGNC ID	HGNC:4325	ENTREZGENE
Human Proteome Map	GLP2R	Human Proteome Map
InterPro	GLP2R	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	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
KEGG Report	hsa:9340	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	9340	ENTREZGENE
OMIM	603659	OMIM
PANTHER	PDF RECEPTOR-LIKE PROTEIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR45620:SF23	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	7tm_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HRM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA28726	PharmGKB
PRINTS	GPCRSECRETIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F2_1	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	A0A384MTS7	ENTREZGENE, UniProtKB/TrEMBL
	B2RAN4	ENTREZGENE, UniProtKB/TrEMBL
	E9PC86_HUMAN	UniProtKB/TrEMBL
	GLP2R_HUMAN	UniProtKB/Swiss-Prot
	H0Y6C2_HUMAN	UniProtKB/TrEMBL
	I3L0P5	ENTREZGENE, UniProtKB/TrEMBL
	O95838	ENTREZGENE
	Q4VAT1_HUMAN	UniProtKB/TrEMBL
	Q4VAT2_HUMAN	UniProtKB/TrEMBL
	Q4VAT3	ENTREZGENE
	Q4VAT4_HUMAN	UniProtKB/TrEMBL
	Q86XI5_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	Q4VAT3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-04-04	GLP2R	glucagon like peptide 2 receptor	GLP2R	glucagon-like peptide 2 receptor	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)

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Imported Disease Annotations - ClinVar