GRM2 (glutamate metabotropic receptor 2)

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Gene: GRM2 (glutamate metabotropic receptor 2) Homo sapiens

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Symbol:

GRM2

Name:

glutamate metabotropic receptor 2

RGD ID:

732930

HGNC Page

HGNC:4594

Description:

Predicted to enable group II metabotropic glutamate receptor activity and scaffold protein binding activity. Predicted to be involved in G protein-coupled glutamate receptor signaling pathway; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and regulation of glutamatergic synaptic transmission. Predicted to act upstream of or within gene expression; intracellular glutamate homeostasis; and long-term synaptic depression. Predicted to be located in astrocyte projection; axon; and presynapse. Predicted to be active in glutamatergic synapse; postsynaptic membrane; and presynaptic membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

GLUR2; glutamate receptor homolog; glutamate receptor, metabotropic 2; GPRC1B; metabotropic glutamate receptor 2; mGlu2; MGLUR2

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	51,707,068 - 51,718,613 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	51,707,068 - 51,718,613 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	51,741,084 - 51,752,629 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	51,718,004 - 51,727,669 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	51,718,037 - 51,727,168	NCBI
Celera	3	51,718,848 - 51,731,506 (+)	NCBI		Celera
Cytogenetic Map	3	p21.2	NCBI
HuRef	3	51,802,839 - 51,816,142 (+)	NCBI		HuRef
CHM1_1	3	51,693,893 - 51,705,447 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	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

amphetamine abuse (EXP)

Binge Drinking (ISO)

Cocaine-Related Disorders (ISO)

heroin dependence (ISO)

schizophrenia (EXP,ISO)

substance-induced psychosis (EXP)

temporal lobe epilepsy (EXP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-pilocarpine (ISO)

(S)-nicotine (ISO)

17beta-estradiol (ISO)

2,3',4,4',5-Pentachlorobiphenyl (ISO)

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

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

4,4'-sulfonyldiphenol (ISO)

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

6-propyl-2-thiouracil (ISO)

acrylamide (EXP)

aflatoxin B1 (EXP)

amiodarone (EXP)

ammonium chloride (ISO)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (ISO)

bisphenol F (ISO)

carbamazepine (EXP)

CGP 52608 (EXP)

chaetocin (ISO)

chlordecone (ISO)

chlorpyrifos (ISO)

cocaine (ISO)

curcumin (ISO)

diazinon (ISO)

entinostat (EXP)

epoxiconazole (ISO)

ethanol (ISO)

ethylparaben (EXP)

fonofos (EXP)

haloperidol (ISO)

mescaline (ISO)

methamphetamine (EXP,ISO)

methylisothiazolinone (EXP)

N-acetyl-L-cysteine (EXP)

nicotine (ISO)

Nonylphenol (ISO)

paraquat (ISO)

parathion (EXP)

permethrin (EXP)

piperidines (ISO)

rotenone (EXP)

sodium arsenite (ISO)

sodium fluoride (ISO)

Soman (ISO)

terbufos (EXP)

titanium dioxide (ISO)

triclosan (EXP)

triptonide (ISO)

tunicamycin (ISO)

valproic acid (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

adenylate cyclase-inhibiting G protein-coupled glutamate receptor signaling pathway (IEA)

behavioral response to nicotine (IEA,ISO)

cellular response to stress (IEA,ISO)

chemical synaptic transmission (TAS)

G protein-coupled glutamate receptor signaling pathway (IBA)

G protein-coupled receptor signaling pathway (IEA)

gene expression (IEA,ISO)

glutamate receptor signaling pathway (IEA)

glutamate secretion (IEA)

intracellular glutamate homeostasis (IEA,ISO)

long-term synaptic depression (IEA,ISO)

negative regulation of adenylate cyclase activity (TAS)

positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction (IEA,ISS)

presynaptic modulation of chemical synaptic transmission (IEA)

regulation of dopamine secretion (IEA,ISO)

regulation of glutamate secretion (IEA,ISO)

regulation of response to drug (IEA,ISO)

regulation of synaptic transmission, glutamatergic (IBA)

response to cocaine (IEA,ISO)

Cellular Component

astrocyte projection (IEA,ISS)

axon (IEA,ISS)

cell projection (IEA)

dendrite (IEA)

glutamatergic synapse (IEA,ISO)

membrane (IEA)

neuron projection (IEA)

plasma membrane (IBA,IEA,TAS)

postsynaptic membrane (IEA,ISO)

presynaptic membrane (IEA,ISO)

synapse (IEA)

Molecular Function

calcium channel regulator activity (IEA)

G protein-coupled receptor activity (IEA,TAS)

glutamate receptor activity (IEA,TAS)

group II metabotropic glutamate receptor activity (IBA,IEA,ISO)

protein binding (IPI)

scaffold protein binding (IEA,ISS)

Molecular Pathway Annotations Click to see Annotation Detail View

glutamate signaling pathway (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	Differences in 5-HT2A and mGlu2 Receptor Expression Levels and Repressive Epigenetic Modifications at the 5-HT2A Promoter Region in the Roman Low- (RLA-I) and High- (RHA-I) Avoidance Rat Strains.	Fomsgaard L, etal., Mol Neurobiol. 2018 Mar;55(3):1998-2012. doi: 10.1007/s12035-017-0457-y. Epub 2017 Mar 6.
2.	Deletion of the type 2 metabotropic glutamate receptor increases heroin abuse vulnerability in transgenic rats.	Gao JT, etal., Neuropsychopharmacology. 2018 Dec;43(13):2615-2626. doi: 10.1038/s41386-018-0231-5. Epub 2018 Oct 3.
3.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
4.	Online Mendelian Inheritance in Man, OMIM (TM).	Online Mendelian Inheritance in Man, OMIM (TM).
5.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
6.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
8.	Ethanol concentration-dependent alterations in gene expression during acute binge drinking in the HIV-1 transgenic rat.	Sarkar S and Chang SL, Alcohol Clin Exp Res. 2013 Jul;37(7):1082-90. doi: 10.1111/acer.12077. Epub 2013 Feb 15.
9.	Deletion of Type 2 Metabotropic Glutamate Receptor Decreases Sensitivity to Cocaine Reward in Rats.	Yang HJ, etal., Cell Rep. 2017 Jul 11;20(2):319-332. doi: 10.1016/j.celrep.2017.06.046.

Additional References at PubMed

PMID:7620613	PMID:8824806	PMID:8863838	PMID:9651375	PMID:11317221	PMID:11641422	PMID:11840499	PMID:11850456	PMID:11891216	PMID:11897108	PMID:12477932	PMID:15035981
PMID:15246118	PMID:15330338	PMID:15489334	PMID:15837331	PMID:16102532	PMID:16344560	PMID:16678921	PMID:18297054	PMID:18853337	PMID:19026996	PMID:19086053	PMID:19156168
PMID:19367581	PMID:19386277	PMID:19402024	PMID:19635471	PMID:19945495	PMID:20211215	PMID:21173788	PMID:21873635	PMID:21881873	PMID:22870276	PMID:22988116	PMID:23129762
PMID:23149219	PMID:23407939	PMID:24080311	PMID:24623722	PMID:24949866	PMID:25150943	PMID:25416956	PMID:25571949	PMID:26589404	PMID:26758213	PMID:27218869	PMID:28319085
PMID:28392297	PMID:29360159	PMID:30326345	PMID:31586073	PMID:31706572	PMID:32296183	PMID:33398167	PMID:34135509	PMID:34135510	PMID:34194039	PMID:34387961	PMID:34521824
PMID:34903715	PMID:36779763	PMID:36889432	PMID:37629122	PMID:38739800

Genomics

Comparative Map Data

GRM2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	51,707,068 - 51,718,613 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	51,741,084 - 51,752,629 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	51,718,004 - 51,727,669 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	51,718,037 - 51,727,168	NCBI
Celera	3	51,718,848 - 51,731,506 (+)	NCBI		Celera
Cytogenetic Map	3	p21.2	NCBI
HuRef	3	51,802,839 - 51,816,142 (+)	NCBI		HuRef
CHM1_1	3	51,693,893 - 51,705,447 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI		T2T-CHM13v2.0

Grm2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	106,521,733 - 106,533,308 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	106,520,294 - 106,533,281 (-)	Ensembl		GRCm39 Ensembl
GRCm38	9	106,644,534 - 106,656,109 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	106,643,095 - 106,656,082 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	106,546,865 - 106,558,440 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	106,546,755 - 106,558,434 (-)	NCBI		MGSCv36	mm8
Celera	9	106,265,562 - 106,277,130 (-)	NCBI		Celera
Cytogenetic Map	9	F1	NCBI
cM Map	9	57.98	NCBI

Grm2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	116,158,810 - 116,171,857 (-)	NCBI		GRCr8
mRatBN7.2	8	107,280,099 - 107,293,159 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	107,280,099 - 107,293,146 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	112,903,031 - 112,916,129 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	111,102,213 - 111,115,309 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	108,944,991 - 108,958,085 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	115,344,999 - 115,358,628 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	8	115,344,999 - 115,358,046 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	8	114,705,123 - 114,718,193 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	8	111,837,086 - 111,850,133 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	8	111,857,819 - 111,869,581 (-)	NCBI
Celera	8	106,592,051 - 106,605,096 (-)	NCBI		Celera
Cytogenetic Map	8	q32	NCBI

Grm2
(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_004955532	3,309,028 - 3,320,966 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955532	3,309,034 - 3,320,954 (+)	NCBI	ChiLan1.0	ChiLan1.0

GRM2
(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	51,694,559 - 51,707,434 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	3	51,699,333 - 51,712,208 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	3	51,639,792 - 51,652,779 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	3	52,873,144 - 52,884,401 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	3	52,873,144 - 52,884,395 (+)	Ensembl	panpan1.1		panPan2

GRM2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	37,915,178 - 37,926,276 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	37,915,665 - 37,924,296 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	37,895,193 - 37,906,256 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	38,264,331 - 38,275,394 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	38,264,304 - 38,275,372 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	37,627,888 - 37,638,953 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	38,036,604 - 38,047,669 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	38,321,755 - 38,332,818 (-)	NCBI		UU_Cfam_GSD_1.0

Grm2
(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	66,281,725 - 66,293,182 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936529	3,042,248 - 3,053,673 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936529	3,042,220 - 3,053,670 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

GRM2
(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	33,926,804 - 33,938,269 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	33,924,303 - 33,938,279 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	13	37,130,553 - 37,141,351 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

GRM2
(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	13,044,974 - 13,056,469 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	22	13,046,641 - 13,056,453 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	153,898,374 - 153,910,372 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Grm2
(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	5,419,896 - 5,431,361 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624730	5,419,892 - 5,431,268 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in GRM2
54 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3p21.31-14.3(chr3:49461000-55314500)x1	copy number loss	See cases [RCV000051511]	Chr3:49461000..55314500 [GRCh38] Chr3:49498433..55348528 [GRCh37] Chr3:49473437..55323568 [NCBI36] Chr3:3p21.31-14.3	pathogenic
NM_000839.3(GRM2):c.1297C>T (p.Arg433Cys)	single nucleotide variant	Malignant melanoma [RCV000066134]	Chr3:51715070 [GRCh38] Chr3:51749086 [GRCh37] Chr3:51724126 [NCBI36] Chr3:3p21.2	not provided
GRCh38/hg38 3p21.2-14.3(chr3:51394434-55064449)x1	copy number loss	See cases [RCV000143631]	Chr3:51394434..55064449 [GRCh38] Chr3:51431865..55098476 [GRCh37] Chr3:51406905..55073516 [NCBI36] Chr3:3p21.2-14.3	likely pathogenic
NM_000839.5(GRM2):c.1354C>T (p.Arg452Cys)	single nucleotide variant	not specified [RCV004315279]	Chr3:51715127 [GRCh38] Chr3:51749143 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1904G>A (p.Arg635Gln)	single nucleotide variant	not specified [RCV004307960]	Chr3:51715677 [GRCh38] Chr3:51749693 [GRCh37] Chr3:3p21.2	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 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
NM_000839.5(GRM2):c.810C>T (p.Thr270=)	single nucleotide variant	not provided [RCV000884704]	Chr3:51712832 [GRCh38] Chr3:51746848 [GRCh37] Chr3:3p21.2	benign
NM_000839.5(GRM2):c.2595G>A (p.Val865=)	single nucleotide variant	not provided [RCV000969012]	Chr3:51718088 [GRCh38] Chr3:51752104 [GRCh37] Chr3:3p21.2	benign
NM_000839.5(GRM2):c.369C>T (p.Asp123=)	single nucleotide variant	not provided [RCV000924029]	Chr3:51709352 [GRCh38] Chr3:51743368 [GRCh37] Chr3:3p21.2	likely benign
NM_000839.5(GRM2):c.1316A>G (p.Asn439Ser)	single nucleotide variant	not provided [RCV000897454]	Chr3:51715089 [GRCh38] Chr3:51749105 [GRCh37] Chr3:3p21.2	benign
NM_000839.5(GRM2):c.2074C>T (p.Leu692Phe)	single nucleotide variant	not provided [RCV000896986]	Chr3:51715847 [GRCh38] Chr3:51749863 [GRCh37] Chr3:3p21.2	likely benign
GRCh37/hg19 3p21.31-21.1(chr3:45153770-53878616)	copy number gain	not provided [RCV000767704]	Chr3:45153770..53878616 [GRCh37] Chr3:3p21.31-21.1	pathogenic
NM_000839.5(GRM2):c.2472C>T (p.Asn824=)	single nucleotide variant	not provided [RCV000962029]	Chr3:51717744 [GRCh38] Chr3:51751760 [GRCh37] Chr3:3p21.2	benign
GRCh37/hg19 3p21.2-21.1(chr3:51247306-53069942)x3	copy number gain	not provided [RCV001005434]	Chr3:51247306..53069942 [GRCh37] Chr3:3p21.2-21.1	uncertain significance
NM_000839.5(GRM2):c.420T>C (p.Ile140=)	single nucleotide variant	not provided [RCV000931551]	Chr3:51709403 [GRCh38] Chr3:51743419 [GRCh37] Chr3:3p21.2	likely benign
NM_000839.5(GRM2):c.2001T>C (p.Gly667=)	single nucleotide variant	not provided [RCV000922644]	Chr3:51715774 [GRCh38] Chr3:51749790 [GRCh37] Chr3:3p21.2	likely benign
NM_000839.5(GRM2):c.888T>C (p.Gly296=)	single nucleotide variant	not provided [RCV000937079]	Chr3:51712910 [GRCh38] Chr3:51746926 [GRCh37] Chr3:3p21.2	likely benign
NM_000839.5(GRM2):c.743C>T (p.Ala248Val)	single nucleotide variant	not provided [RCV000913640]	Chr3:51712765 [GRCh38] Chr3:51746781 [GRCh37] Chr3:3p21.2	likely benign
NM_000839.5(GRM2):c.1495C>T (p.Arg499Cys)	single nucleotide variant	not specified [RCV004117344]	Chr3:51715268 [GRCh38] Chr3:51749284 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.374C>A (p.Ser125Tyr)	single nucleotide variant	not specified [RCV004164783]	Chr3:51709357 [GRCh38] Chr3:51743373 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1346G>A (p.Gly449Asp)	single nucleotide variant	not specified [RCV004224299]	Chr3:51715119 [GRCh38] Chr3:51749135 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.130G>A (p.Gly44Ser)	single nucleotide variant	not specified [RCV004093050]	Chr3:51709113 [GRCh38] Chr3:51743129 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1394G>A (p.Arg465His)	single nucleotide variant	not specified [RCV004182294]	Chr3:51715167 [GRCh38] Chr3:51749183 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1066A>G (p.Ser356Gly)	single nucleotide variant	not specified [RCV004216369]	Chr3:51713088 [GRCh38] Chr3:51747104 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1037G>A (p.Arg346His)	single nucleotide variant	not specified [RCV004189944]	Chr3:51713059 [GRCh38] Chr3:51747075 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2363G>A (p.Arg788Gln)	single nucleotide variant	not specified [RCV004203170]	Chr3:51716136 [GRCh38] Chr3:51750152 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.842C>T (p.Ala281Val)	single nucleotide variant	not specified [RCV004112933]	Chr3:51712864 [GRCh38] Chr3:51746880 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.975T>A (p.Ser325Arg)	single nucleotide variant	not specified [RCV004185339]	Chr3:51712997 [GRCh38] Chr3:51747013 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1709G>A (p.Gly570Glu)	single nucleotide variant	not specified [RCV004119802]	Chr3:51715482 [GRCh38] Chr3:51749498 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1399C>T (p.Arg467Cys)	single nucleotide variant	not specified [RCV004206099]	Chr3:51715172 [GRCh38] Chr3:51749188 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.133G>A (p.Gly45Ser)	single nucleotide variant	not specified [RCV004219021]	Chr3:51709116 [GRCh38] Chr3:51743132 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2138G>A (p.Arg713Gln)	single nucleotide variant	not specified [RCV004128247]	Chr3:51715911 [GRCh38] Chr3:51749927 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2460G>T (p.Gln820His)	single nucleotide variant	not specified [RCV004167420]	Chr3:51717732 [GRCh38] Chr3:51751748 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1886C>T (p.Thr629Met)	single nucleotide variant	not specified [RCV004229137]	Chr3:51715659 [GRCh38] Chr3:51749675 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1469C>T (p.Pro490Leu)	single nucleotide variant	not specified [RCV004203517]	Chr3:51715242 [GRCh38] Chr3:51749258 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2491C>A (p.Pro831Thr)	single nucleotide variant	not specified [RCV004143125]	Chr3:51717763 [GRCh38] Chr3:51751779 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1087G>A (p.Ala363Thr)	single nucleotide variant	not specified [RCV004181967]	Chr3:51713109 [GRCh38] Chr3:51747125 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.97G>A (p.Val33Met)	single nucleotide variant	not specified [RCV004212439]	Chr3:51709080 [GRCh38] Chr3:51743096 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.603C>G (p.Phe201Leu)	single nucleotide variant	not specified [RCV004175686]	Chr3:51712625 [GRCh38] Chr3:51746641 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1612G>A (p.Ala538Thr)	single nucleotide variant	not specified [RCV004075350]	Chr3:51715385 [GRCh38] Chr3:51749401 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2171G>A (p.Arg724His)	single nucleotide variant	not specified [RCV004091285]	Chr3:51715944 [GRCh38] Chr3:51749960 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1592G>A (p.Arg531Gln)	single nucleotide variant	not specified [RCV004075475]	Chr3:51715365 [GRCh38] Chr3:51749381 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2432C>T (p.Ala811Val)	single nucleotide variant	not specified [RCV004261481]	Chr3:51717704 [GRCh38] Chr3:51751720 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.560C>T (p.Pro187Leu)	single nucleotide variant	not specified [RCV004271260]	Chr3:51712582 [GRCh38] Chr3:51746598 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.589G>C (p.Glu197Gln)	single nucleotide variant	not specified [RCV004269474]	Chr3:51712611 [GRCh38] Chr3:51746627 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.599G>A (p.Arg200His)	single nucleotide variant	not specified [RCV004345566]	Chr3:51712621 [GRCh38] Chr3:51746637 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1762G>A (p.Val588Ile)	single nucleotide variant	not specified [RCV004346341]	Chr3:51715535 [GRCh38] Chr3:51749551 [GRCh37] Chr3:3p21.2	uncertain significance
GRCh37/hg19 3p21.2-14.2(chr3:51149374-59265315)x1	copy number loss	not specified [RCV003986409]	Chr3:51149374..59265315 [GRCh37] Chr3:3p21.2-14.2	pathogenic
NM_000839.5(GRM2):c.1994G>A (p.Arg665Gln)	single nucleotide variant	not specified [RCV004396030]	Chr3:51715767 [GRCh38] Chr3:51749783 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2228C>T (p.Thr743Met)	single nucleotide variant	not specified [RCV004396032]	Chr3:51716001 [GRCh38] Chr3:51750017 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1907G>A (p.Arg636His)	single nucleotide variant	not specified [RCV004396029]	Chr3:51715680 [GRCh38] Chr3:51749696 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2441T>C (p.Leu814Pro)	single nucleotide variant	not specified [RCV004396033]	Chr3:51717713 [GRCh38] Chr3:51751729 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2597A>G (p.Asp866Gly)	single nucleotide variant	not specified [RCV004396035]	Chr3:51718090 [GRCh38] Chr3:51752106 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1064G>A (p.Cys355Tyr)	single nucleotide variant	not specified [RCV004396026]	Chr3:51713086 [GRCh38] Chr3:51747102 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.736A>G (p.Ser246Gly)	single nucleotide variant	not specified [RCV004396038]	Chr3:51712758 [GRCh38] Chr3:51746774 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1400G>A (p.Arg467His)	single nucleotide variant	not specified [RCV004396028]	Chr3:51715173 [GRCh38] Chr3:51749189 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1289C>T (p.Ala430Val)	single nucleotide variant	not specified [RCV004396027]	Chr3:51715062 [GRCh38] Chr3:51749078 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2080G>A (p.Val694Met)	single nucleotide variant	not specified [RCV004396031]	Chr3:51715853 [GRCh38] Chr3:51749869 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2485C>T (p.Arg829Trp)	single nucleotide variant	not specified [RCV004396034]	Chr3:51717757 [GRCh38] Chr3:51751773 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.430T>G (p.Tyr144Asp)	single nucleotide variant	not specified [RCV004396036]	Chr3:51709413 [GRCh38] Chr3:51743429 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2141G>A (p.Arg714Gln)	single nucleotide variant	not specified [RCV004634892]	Chr3:51715914 [GRCh38] Chr3:51749930 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1073G>T (p.Arg358Leu)	single nucleotide variant	not specified [RCV004624053]	Chr3:51713095 [GRCh38] Chr3:51747111 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2158C>T (p.Arg720Cys)	single nucleotide variant	not specified [RCV004624054]	Chr3:51715931 [GRCh38] Chr3:51749947 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.811C>T (p.Arg271Cys)	single nucleotide variant	not specified [RCV004624055]	Chr3:51712833 [GRCh38] Chr3:51746849 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2398C>T (p.Leu800Phe)	single nucleotide variant	not specified [RCV004634891]	Chr3:51717670 [GRCh38] Chr3:51751686 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.49G>A (p.Val17Met)	single nucleotide variant	not specified [RCV004634890]	Chr3:51709032 [GRCh38] Chr3:51743048 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.923A>T (p.Glu308Val)	single nucleotide variant	not specified [RCV004634893]	Chr3:51712945 [GRCh38] Chr3:51746961 [GRCh37] Chr3:3p21.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2573
Count of miRNA genes:	957
Interacting mature miRNAs:	1155
Transcripts:	ENST00000296479, ENST00000395052, ENST00000419928, ENST00000442933, ENST00000464585, ENST00000475478, ENST00000477330, ENST00000496661
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
406976176	GWAS625152_H	macrophage inflammatory protein 1b measurement QTL GWAS625152 (human)		5e-10	macrophage inflammatory protein 1b measurement		3	51713272	51713273	Human
1298487	BFD1_H	Body fluid distribution QTL 1 (human)	3.94		Body fluid distribution	impedance ratio	3	36380712	62380712	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
2289308	BW392_H	Body weight QTL 392 (human)	1.42		Body weight	BMI	3	36380712	62380712	Human
1331643	COPD16_H	Chronic obstructive pulmonary disease QTL 16 (human)	1.07		Chronic airflow obstruction	post-BD FEV1 minus pre-BD FEV1/pre-BD FEV1 x 100	3	49380651	75380651	Human

Markers in Region

WI-20087

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	51,752,274 - 51,752,544	UniSTS	GRCh37
Build 36	3	51,727,314 - 51,727,584	RGD	NCBI36
Celera	3	51,731,151 - 51,731,421	RGD
Cytogenetic Map	3	p21.2	UniSTS
HuRef	3	51,815,787 - 51,816,057	UniSTS
GeneMap99-GB4 RH Map	3	160.13	UniSTS
Whitehead-RH Map	3	211.7	UniSTS

RH66405

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	51,752,321 - 51,752,463	UniSTS	GRCh37
Build 36	3	51,727,361 - 51,727,503	RGD	NCBI36
Celera	3	51,731,198 - 51,731,340	RGD
Cytogenetic Map	3	p21.2	UniSTS
HuRef	3	51,815,834 - 51,815,976	UniSTS
GeneMap99-GB4 RH Map	3	161.32	UniSTS

A002C19

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	51,752,331 - 51,752,502	UniSTS	GRCh37
Build 36	3	51,727,371 - 51,727,542	RGD	NCBI36
Celera	3	51,731,208 - 51,731,379	RGD
Cytogenetic Map	3	p21.2	UniSTS
HuRef	3	51,815,844 - 51,816,015	UniSTS
GeneMap99-GB4 RH Map	3	161.32	UniSTS

GRM2

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	51,746,554 - 51,746,750	UniSTS	GRCh37
Build 36	3	51,721,594 - 51,721,790	RGD	NCBI36
Celera	3	51,725,429 - 51,725,625	RGD
HuRef	3	51,810,065 - 51,810,261	UniSTS

SHGC-77001

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	3	p21.2	UniSTS
TNG Radiation Hybrid Map	3	32009.0	UniSTS
GeneMap99-GB4 RH Map	3	162.92	UniSTS
NCBI RH Map	3	494.1	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	visual system
1202	2352	2787	2234	4899	1619	2174	1	533	1557	372	2223	6646	6051	45	3711	752	1695	1532	170	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_000839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001349116	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001349117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_146059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533636	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017006271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024453490	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448048	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448049	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346368	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346372	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346373	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346374	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346375	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346376	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054346377	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB045011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB209164	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC099050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289984	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313056	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY999299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC041447	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC113615	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC113619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648951	(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
	DA391442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA528713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EU432122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L35318	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000296479 ⟹ ENSP00000296479

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,707,088 - 51,718,112 (+)	Ensembl

Ensembl Acc Id:

ENST00000395052 ⟹ ENSP00000378492

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,707,068 - 51,718,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000419928 ⟹ ENSP00000404797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,707,411 - 51,709,193 (+)	Ensembl

Ensembl Acc Id:

ENST00000442933 ⟹ ENSP00000408906

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,708,845 - 51,718,252 (+)	Ensembl

Ensembl Acc Id:

ENST00000464585

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,707,305 - 51,718,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000475478

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,707,090 - 51,718,613 (+)	Ensembl

Ensembl Acc Id:

ENST00000477330

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,711,272 - 51,712,581 (+)	Ensembl

Ensembl Acc Id:

ENST00000496661

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	51,711,272 - 51,714,068 (+)	Ensembl

RefSeq Acc Id:

NM_000839 ⟹ NP_000830

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI
GRCh37	3	51,741,081 - 51,752,629 (+)	ENTREZGENE
Build 36	3	51,718,004 - 51,727,669 (+)	NCBI Archive
HuRef	3	51,802,839 - 51,816,142 (+)	ENTREZGENE
CHM1_1	3	51,693,893 - 51,705,447 (+)	NCBI
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI

Sequence:

show sequence

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCC
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGAGCTGGGTCCCTTCGCATCTCTCTTCT
TGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCC
CTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGCTGCTTGCGCT
CCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTG
GAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCAGCAGAGGACT
GTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCG
CATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCTCGACAGTTGC
TCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTG
CTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATGCTCCCACTGC
CATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGG
CTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCT
ATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCT
CCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGC
ATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGG
GCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGC
CCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGC
CTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAG
GCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTT
TGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTC
TGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTG
TGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGC
GCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCA
GTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCC
CAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACAT
CTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAA
GGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCT
CTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTG
CTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGT
GGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCC
GCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCT
CTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAG
CTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCA
AGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTA
CTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCC
CAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCC
AGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCC
CGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTG
GCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCG
AAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGC
ATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTG
TCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCC
TCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGC
TGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAAT
GGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACAC
AGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACT
GCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGC
TCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTG
TAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCC
CTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAG
CCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGG
TTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCT
GTAAATAAAGTGGCTTTATTTTAAAAAA

hide sequence

RefSeq Acc Id:

NM_001349116 ⟹ NP_001336045

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI

Sequence:

show sequence

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCC
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGAGCCTGGACCCTTGGAACAACAGCCGGA
ACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGC
AGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCA
GTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGC
TCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAA
GTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGAT
GGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGA
AGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTC
AGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTG
CAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACG
AATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGA
ACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGC
CTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGG
TCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCAT
GACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGC
ACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCG
GTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTG
CCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGC
ACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATG
CAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTT
CAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACC
ACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTAC
AGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGC
GCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACC
AGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGT
TTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACC
CCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGG
AGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTT
ACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCA
GTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGC
AAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAG
CAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTA
CTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTG
TGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAA

hide sequence

RefSeq Acc Id:

NM_001349117 ⟹ NP_001336046

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI

Sequence:

show sequence

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCC
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGAGCTGGGTCCCTTCGCATCTCTCTTCT
TGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCC
CTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGCTGCTTGCGCT
CCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTG
GAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCAGCAGAGGACT
GTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCG
CATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCTCGACAGTTGC
TCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTG
CTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATGCTCCCACTGC
CATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGG
CTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCT
ATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCT
CCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGC
ATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGG
GCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGC
CCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGC
CTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAG
GCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTT
TGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTC
TGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTG
TGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGC
GCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCA
GTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGGTGACCTGAAAG
TCTCCTGAAATCAAAAGTTATTTTAATAAGAGTGCCAGCTTTAAGAGAAATGACTGCTGCAGAT
CATCACTATGCTTCAGGAAGAATCACCGTGGGAACAGTGGGAGACAAAGCTTGGAAGCCCTGGC
CCAGGGTTAAGATGAAGACCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCG
CTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTAT
CGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGG
CCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGT
GAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTAC
CGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTG
GCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCAC
CATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCC
ACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCT
GCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCT
TGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCA
CGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGG
TGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGA
GGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAAC
CACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGC
TTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCAC
CATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGAC
TACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCT
GCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCG
GGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCT
GGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGC
TTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTC
CAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCC
AAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGG
AGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTC
AGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAG
TCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTT
ATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTA
GTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAA

hide sequence

RefSeq Acc Id:

NR_146059

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI

Sequence:

show sequence

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCC
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGCCCCCTTTCGCCCAGCTGACACCCACAA
TGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGT
GCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACA
CCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCC
CTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCG
TGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGC
CCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTG
GGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTC
TTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGC
TGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGT
GTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACC
AAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCA
TCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGT
CGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTG
GTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCC
TCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGC
CAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTC
TATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCG
GCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAA
GAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCC
AGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGG
ACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAAC
CTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACC
CACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAG
TCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCC
TGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCT
GAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTA
GGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGC
CCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTT
TATTTTAAAAAA

hide sequence

RefSeq Acc Id:

XM_011533636 ⟹ XP_011531938

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI

Sequence:

show sequence

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCG
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGA
GGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGC
CCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTT
CCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAA
ATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCA
GGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAA
GAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTC
ACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCT
TGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTT
GCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGC
TTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTG
GAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTT
CTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTC
CAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAG
AGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCC
CACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGA
CAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGG
CTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGG
TTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCA
TCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTA
ATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGC
TGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGT
GCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCA
GCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTG
CACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCT
CGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTC
AGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATG
CTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGAGCCTGGA
CCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGC
TTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGA
TCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCT
CTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAG
GACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCC
GCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAG
TGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTC
ATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCC
AGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCC
CTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCC
AGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGG
GACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCG
GCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGT
GTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCT
TACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAA
CCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCT
GCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGC
TGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACT
GCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCG
CTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCA
TTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCAC
CTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTG
GTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGG
TTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGG
CCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACA
ACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCA
GACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTAT
GTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGC
CTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGG
CCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGG
CAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTT
TTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCC
CTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAA
AAAATCA

hide sequence

RefSeq Acc Id:

XM_011533637 ⟹ XP_011531939

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,710,699 - 51,718,613 (+)	NCBI

Sequence:

show sequence

TGTTCAGGAGAAATGGAGCAGAAGCAGAAATCAGAGAACCCTGGAGTCAGCTACCGGCCTGAAG
TCGGGGAGGCCTGGCCACTCCATCCACTGCTGGGAGTGGATTATCTGTCCTGCTAATCCCAGAC
ACTGGAGGTGGCTAGGCAGCTGTCATGCTAGTCTCAGTCACTGGAGGTGGCTAGGCAGCTGTCC
TGCTAGTCCCAGTCACTGGAGGTGGCTAGGCAGCAGCCTGGGAAGATGTGGCTGTGCTAGCATC
TATTTCTGCAGCCCCGGGTTGGGGCAGGGATGAGTGGGCGGCCTCCTACCTGCTGCTGTCTTCC
AGGGCCTCTGCTGAAGTTTTCTCCACAGTCCTCCTTAGGGCTCATGCATTTATCTCCAGAAGTC
CAGTTACCTCCTTGCCATCCCAAGCTGCCTGCCTCCTGGATCAGGGCCCACGCCTCAGCAGTGG
TCTGCTTCTCCCTCGTCCTGATCAACACGAGGCTAGCCTGTCATCCGTAGGCTGCACCTGCCTG
TTAATATTCCCCCTCATGGCTGCTCCTTCTCTCTTGCCCATGTCCCTATCATCTTCCCTTTGCC
AGGCACTGTGGCCTCCCATGCATTATCGTTTTTATCCTCTCAGCAGCCTTGTAGGGCAGGAATG
TGAAACTGAGGCTCAGGGAGATTTGCCAACTCCAGGGGCCCAAAGGTGGCCAACCTCTTGAGGC
TATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCTA
TGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTC
CGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGCA
TTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGG
CCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGCC
CGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCC
TCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAGG
CAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTT
GCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCT
GGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGT
GCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCG
CTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAG
TTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCC
AGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATC
TTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAG
GCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTC
TCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGC
TGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTG
GCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCG
CTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTC
TTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGC
TCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAA
GCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTAC
TCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCC
AGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCA
GCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCC
GAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGG
CCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGA
AAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCA
TTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGT
CAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCT
CTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCT
GCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATG
GCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACA
GCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTG
CAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCT
CTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGT
AGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCC
TGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGC
CCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGT
TATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTG
TAAATAAAGTGGCTTTATTTTAAAAAATCA

hide sequence

RefSeq Acc Id:

XM_011533642 ⟹ XP_011531944

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,715,367 (+)	NCBI

Sequence:

show sequence

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCG
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGA
GGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGC
CCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTT
CCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAA
ATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCA
GGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAA
GAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTC
ACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCT
TGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTT
GCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGC
TTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTG
GAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTT
CTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTC
CAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAG
AGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCC
CACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGA
CAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGG
CTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGG
TTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCA
TCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTA
ATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGC
TGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGT
GCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCA
GCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTG
CACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCT
CGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTC
AGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATG
CTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAA
CCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGAC
AAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGG
CTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGG
CGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCG
GAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGA
AGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGC
CAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGT
GTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCA
TCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTT
CCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCT
CTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCA
TGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGC
GATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCC
CCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCC
GCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGTGAGCCCT
GCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTG
CCAGCCCTATGAGTACCGAT

hide sequence

RefSeq Acc Id:

XM_011533643 ⟹ XP_011531945

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,713,223 - 51,718,613 (+)	NCBI

Sequence:

show sequence

CCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACT
TTGTGCTCAACGTCAAGTTTGATGGTGACCTGAAAGTCTCCTGAAATCAAAAGTTATTTTAATA
AGAGTGCCAGCTTTAAGAGAAATGACTGCTGCAGATCATCACTATGCTTCAGGAAGAATCACCG
TGGGAACAGTGGGAGACAAAGCTTGGAAGCCCTGGCCCAGGCCCCCTTTCGCCCAGCTGACACC
CACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATC
TGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGTGAGCCCTGCCTCCAGAATGAGGTGAAGA
GTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATT
GGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGC
TTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCG
CCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACC
AGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTAC
TGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTT
TGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCAT
CTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCC
ATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCAC
CGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCG
CGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTAT
GCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGT
ACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCG
GGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTC
TTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCAC
CCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTC
CCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGA
AGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGG
CCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGT
CACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCT
CTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGA
GGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTA
ACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATA
AGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTG
TCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAATCA

hide sequence

RefSeq Acc Id:

XM_017006271 ⟹ XP_016861760

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI

Sequence:

show sequence

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCG
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGAGCTGGGTCCCTTCGCATCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCC
TCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCAT
CCCCTTTGGGGCCATGGGATCGCTGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTG
GCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCC
CAGTGCACCAGAAGGGCGGCCCAGCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCA
GCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGC
GTGCGCCTGGGTGCACACATCCTCGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCAC
TGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGG
CTCTTATGCGACCCATGGTGATGCTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGT
GATGTCTCCATCCAGGTGGCCAACCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCT
CTACCAGTGCCAAGCTGAGTGACAAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGA
CTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACT
GTGGCGTCTGAGGGCGACTATGGCGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCC
GCAACATCTGTGTGGCCACCTCGGAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGG
TGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAG
GATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTG
ATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCAC
CATCGAGCTGGCCTCCTACCCCATCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGG
AACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGC
AGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTT
TGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCC
AACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTG
TGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGA
CCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGC
TATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCAT
GGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGA
GGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAG
TACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGA
CTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGT
CACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAAT
GCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCC
TCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCG
TCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATT
GCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCAC
AGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGT
GGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGC
AACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCA
CGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTT
CACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGT
GACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTG
GCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCA
CCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGG
TCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCAT
CGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCAC
GTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCC
CCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCC
AGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGG
CTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCC
CAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTT
TTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACA
GTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAATCA

hide sequence

RefSeq Acc Id:

XM_024453490 ⟹ XP_024309258

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,715,268 (+)	NCBI

Sequence:

show sequence

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCG
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGA
GGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGC
CCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTT
CCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAA
ATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCA
GGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAA
GAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTC
ACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCT
TGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTT
GCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGC
TTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTG
GAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTT
CTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTC
CAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAG
AGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCC
CACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGA
CAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGG
CTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGG
TTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCA
TCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTA
ATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGC
TGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGT
GCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCA
GCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTG
CACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCT
CGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTC
AGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATG
CTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAA
CCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGAC
AAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGG
CTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGG
CGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCG
GAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGA
AGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGC
CAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGT
GTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCA
TCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTT
CCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCT
CTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCA
TGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGC
GATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGGT
GACCTGAAAGTCTCCTGAAATCAAAAGTTATTTTAATAAGAGTGCCAGCTTTAAGAGAAATGAC
TGCTGCAGATCATCACTATGCTTCAGGAAGAATCACCGTGGGAACAGTGGGAGACAAAGCTTGG
AAGCCCTGGCCCAGGGTTAAGATGAAGAGTACTTCCAATAGAACTGACATTCAGAGTTAGCTAC
AATCAGTGTAGGGGTTAGGGTTGGAATCTGGGGTCCGATTTGGTTGATGTTAGAGCAAGGCTAA
ATTCAGCATGTTTGGCTTGGGTGGAATTTATGGTAGGGCTAGAGTTGGATTTTGAGAACTTTTA
GGCTGAGTAGAAAGAGTAGGTGCTTGAGGGGACCTGGGTTTGAATCTAGGCTGCACTATTCACT
CATGGGGCCTTAAGCATGTCTTCTGCTTTCTTGAACCCTGATTTCTCACTGGGGCCAGGGATGG
CTGTAAATCCTGGCTAGAGCCTGGCTGGGAGATGTGAGGTTTACAGGGGATGAAGTGGGGGTGG
AGAGAGGAAGTGATTTTCCAGCCACTGACCACATTCTGGTGAATGGCAGTGGTTGCAGGTGACC
AGTGAGGTTGGGATTCAGTTTGCACCAGGATGACTGTTAGGACTAGGGGTGCTGGAGCTGGGGT
TGTTGTTAGGATTAGTGGGGACAGGATTGGAGCTGAGACTGGGTTTAGCCTTAGCATTGAGTTT
GGGGAGAGGGCTGTAGTGTATGTTTCGATGAAGTTGGGATTTGGAGCCTGGGTTGGAAAGTGTT
GGATAGTACTAAAGTTGAATTTGGGGAGTCATGGTTGGGGATTGATGTGGGCATTAGGTTTTTG
GAGATGTCTGGGCTTTAAGGCTGGGATTACATTTGGCATTTAGGGTTGGGGTTTGATGTTGGAG
TTTAGGAGTAAGACTTTGTTGTCATCTCTCATTTAGAAAAATGATTGGGGTCAAGGCAGGATTT
AGTATTGGGTTAAGGATTGGAAGGGCTAATGGTGGTCTTAGCTCTGGCATTTGGGTTCCATGTT
AGGGTGAATGTTGAGGTCACATCAGGGTAACACACTAGTCCAACCTTCTCTTCCTTCCCTCCCC
CATCCTAGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGAT
GGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGA
AGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTC
AGCCGGCCCCCTGCCCGCCTCTC

hide sequence

RefSeq Acc Id:

XM_047448047 ⟹ XP_047304003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI

RefSeq Acc Id:

XM_047448048 ⟹ XP_047304004

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,709,373 - 51,718,613 (+)	NCBI

RefSeq Acc Id:

XM_047448049 ⟹ XP_047304005

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,709,399 - 51,718,613 (+)	NCBI

RefSeq Acc Id:

XM_047448050 ⟹ XP_047304006

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,709,406 - 51,718,613 (+)	NCBI

RefSeq Acc Id:

XM_047448051 ⟹ XP_047304007

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,709,369 - 51,718,613 (+)	NCBI

RefSeq Acc Id:

XM_054346367 ⟹ XP_054202342

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,738,584 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346368 ⟹ XP_054202343

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346369 ⟹ XP_054202344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,738,584 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346370 ⟹ XP_054202345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,743,691 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346371 ⟹ XP_054202346

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,740,883 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346372 ⟹ XP_054202347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,740,909 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346373 ⟹ XP_054202348

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,740,916 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346374 ⟹ XP_054202349

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,740,879 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346375 ⟹ XP_054202350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,738,584 - 51,748,359 (+)	NCBI

RefSeq Acc Id:

XM_054346376 ⟹ XP_054202351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,746,215 - 51,751,605 (+)	NCBI

RefSeq Acc Id:

XM_054346377 ⟹ XP_054202352

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	51,738,584 - 51,748,260 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_000830	(Get FASTA)	NCBI Sequence Viewer
	NP_001336045	(Get FASTA)	NCBI Sequence Viewer
	NP_001336046	(Get FASTA)	NCBI Sequence Viewer
	XP_011531938	(Get FASTA)	NCBI Sequence Viewer
	XP_011531939	(Get FASTA)	NCBI Sequence Viewer
	XP_011531944	(Get FASTA)	NCBI Sequence Viewer
	XP_011531945	(Get FASTA)	NCBI Sequence Viewer
	XP_016861760	(Get FASTA)	NCBI Sequence Viewer
	XP_024309258	(Get FASTA)	NCBI Sequence Viewer
	XP_047304003	(Get FASTA)	NCBI Sequence Viewer
	XP_047304004	(Get FASTA)	NCBI Sequence Viewer
	XP_047304005	(Get FASTA)	NCBI Sequence Viewer
	XP_047304006	(Get FASTA)	NCBI Sequence Viewer
	XP_047304007	(Get FASTA)	NCBI Sequence Viewer
	XP_054202342	(Get FASTA)	NCBI Sequence Viewer
	XP_054202343	(Get FASTA)	NCBI Sequence Viewer
	XP_054202344	(Get FASTA)	NCBI Sequence Viewer
	XP_054202345	(Get FASTA)	NCBI Sequence Viewer
	XP_054202346	(Get FASTA)	NCBI Sequence Viewer
	XP_054202347	(Get FASTA)	NCBI Sequence Viewer
	XP_054202348	(Get FASTA)	NCBI Sequence Viewer
	XP_054202349	(Get FASTA)	NCBI Sequence Viewer
	XP_054202350	(Get FASTA)	NCBI Sequence Viewer
	XP_054202351	(Get FASTA)	NCBI Sequence Viewer
	XP_054202352	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA76855	(Get FASTA)	NCBI Sequence Viewer
	AAH41447	(Get FASTA)	NCBI Sequence Viewer
	AAI13616	(Get FASTA)	NCBI Sequence Viewer
	AAI13620	(Get FASTA)	NCBI Sequence Viewer
	AAY14640	(Get FASTA)	NCBI Sequence Viewer
	ABY87921	(Get FASTA)	NCBI Sequence Viewer
	BAB19817	(Get FASTA)	NCBI Sequence Viewer
	BAD92401	(Get FASTA)	NCBI Sequence Viewer
	BAF82673	(Get FASTA)	NCBI Sequence Viewer
	BAF98707	(Get FASTA)	NCBI Sequence Viewer
	BAG63904	(Get FASTA)	NCBI Sequence Viewer
	EAW65150	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000296479
	ENSP00000296479.5
	ENSP00000378492
	ENSP00000378492.3
	ENSP00000404797.1
	ENSP00000408906.2
GenBank Protein	Q14416	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_000830 ⟸ NM_000839
- Peptide Label:	isoform a precursor
- UniProtKB:	Q52MC6 (UniProtKB/Swiss-Prot), Q14CU5 (UniProtKB/Swiss-Prot), B0M0K7 (UniProtKB/Swiss-Prot), Q9H3N6 (UniProtKB/Swiss-Prot), Q14416 (UniProtKB/Swiss-Prot), A8K1R9 (UniProtKB/TrEMBL), B0AZM5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGD GIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSV QPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIAC LGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLG TAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPG TGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYT TCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPT SRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL hide sequence

RefSeq Acc Id:

XP_011531938 ⟸ XM_011533636

- Peptide Label:

isoform X3

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA
MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT
HGDAPTAITGVIGGSYSDVSIQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQ
ESKIMFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTH
NEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSE
PCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDA
WAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTA
VCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIV
VAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNE
AKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQ
KNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531944 ⟸ XM_011533642

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA
MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT
HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA
KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA
LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA
SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA
VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGD
GIGRYNIFTYLRAGSGRYRYQK

hide sequence

RefSeq Acc Id:

XP_011531939 ⟸ XM_011533637

- Peptide Label:

isoform X4

- Sequence:

show sequence

MAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRALL
QKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELASY
PISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNAVY
AMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGDGI
GRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQP
GEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLG
ALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTA
FSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTG
KETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTC
IIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSR
FGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531945 ⟸ XM_011533643

- Peptide Label:

isoform X6

- Sequence:

show sequence

MTAADHHYASGRITVGTVGDKAWKPWPRPPFAQLTPTMRSALTALVMVLAATTSSPICVQAVGA
IATRSEPCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEY
IRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFI
AKPSTAVCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALIS
GQLLIVVAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKC
PENFNEAKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHI
ILFQPQKNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:	XP_016861760 ⟸ XM_017006271
- Peptide Label:	isoform X1
- UniProtKB:	Q52MC6 (UniProtKB/Swiss-Prot), Q14CU5 (UniProtKB/Swiss-Prot), B0M0K7 (UniProtKB/Swiss-Prot), Q9H3N6 (UniProtKB/Swiss-Prot), Q14416 (UniProtKB/Swiss-Prot), A8K1R9 (UniProtKB/TrEMBL), B0AZM5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGD GIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSV QPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIAC LGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLG TAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPG TGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYT TCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPT SRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL hide sequence

RefSeq Acc Id:	NP_001336046 ⟸ NM_001349117
- Peptide Label:	isoform d
- UniProtKB:	Q86YG3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTAADHHYASGRITVGTVGDKAWKPWPRVKMKTPFRPADTHNEVRFDRFGDGIGRYNIFTYLRA GSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQPGEVCCWLCIPC QPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLGALATLFVLGVF VRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTAFSVCYSALLTK TNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTGKETAPERREVV TLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTCIIWLAFLPIFY VTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSRFGSAAARASSS LGQGSGSQFVPTVCNGREVVDSTTSSL hide sequence

RefSeq Acc Id:	NP_001336045 ⟸ NM_001349116
- Peptide Label:	isoform c
- UniProtKB:	Q86YG3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVR FDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQ NEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVG PVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTL RRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWL VVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFI GFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVV SHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL hide sequence

RefSeq Acc Id:	XP_024309258 ⟸ XM_024453490
- Peptide Label:	isoform X7
- UniProtKB:	H7BXL3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDGDLKVS hide sequence

Ensembl Acc Id:

ENSP00000296479 ⟸ ENST00000296479

Ensembl Acc Id:

ENSP00000408906 ⟸ ENST00000442933

Ensembl Acc Id:

ENSP00000404797 ⟸ ENST00000419928

Ensembl Acc Id:

ENSP00000378492 ⟸ ENST00000395052

RefSeq Acc Id:	XP_047304003 ⟸ XM_047448047
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047304007 ⟸ XM_047448051
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047304004 ⟸ XM_047448048
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047304005 ⟸ XM_047448049
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047304006 ⟸ XM_047448050
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202343 ⟸ XM_054346368
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054202344 ⟸ XM_054346369
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054202342 ⟸ XM_054346367
- Peptide Label:	isoform X1
- UniProtKB:	Q9H3N6 (UniProtKB/Swiss-Prot), Q52MC6 (UniProtKB/Swiss-Prot), Q14CU5 (UniProtKB/Swiss-Prot), Q14416 (UniProtKB/Swiss-Prot), B0M0K7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054202350 ⟸ XM_054346375
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054202352 ⟸ XM_054346377
- Peptide Label:	isoform X7
- UniProtKB:	H7BXL3 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054202349 ⟸ XM_054346374
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202346 ⟸ XM_054346371
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202347 ⟸ XM_054346372
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202348 ⟸ XM_054346373
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202345 ⟸ XM_054346370
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054202351 ⟸ XM_054346376
- Peptide Label:	isoform X6

Protein Domains

G-protein coupled receptors family 3 profile Receptor ligand binding region

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q14416-F1-model_v2	AlphaFold	Q14416	1-872	view protein structure

Promoters

RGD ID:

6864566

Promoter ID:

EPDNEW_H5448

Type:

initiation region

Name:

GRM2_1

Description:

glutamate metabotropic receptor 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H5449

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,067 - 51,707,127	EPDNEW

RGD ID:

6864568

Promoter ID:

EPDNEW_H5449

Type:

multiple initiation site

Name:

GRM2_2

Description:

glutamate metabotropic receptor 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H5448

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	51,707,249 - 51,707,309	EPDNEW

RGD ID:

6801106

Promoter ID:

HG_KWN:45181

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

NB4

Transcripts:

ENST00000296479, NM_000839, OTTHUMT00000346544, OTTHUMT00000346545, OTTHUMT00000346546, OTTHUMT00000346548, UC003DBP.1, UC010HLU.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	3	51,718,041 - 51,718,541 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:4594	AgrOrtholog
COSMIC	GRM2	COSMIC
Ensembl Genes	ENSG00000164082	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000296479	ENTREZGENE
	ENST00000296479.9	UniProtKB/TrEMBL
	ENST00000395052	ENTREZGENE
	ENST00000395052.8	UniProtKB/Swiss-Prot
	ENST00000419928.1	UniProtKB/TrEMBL
	ENST00000442933.2	UniProtKB/TrEMBL
	ENST00000475478	ENTREZGENE
Gene3D-CATH	2.10.50.30	UniProtKB/Swiss-Prot
	3.40.50.2300	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR, family 3, nine cysteines domain	UniProtKB/TrEMBL
GTEx	ENSG00000164082	GTEx
HGNC ID	HGNC:4594	ENTREZGENE
Human Proteome Map	GRM2	Human Proteome Map
InterPro	ANF_lig-bd_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_9-Cys_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_9-Cys_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_mtglu_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_mtglu_rcpt_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	mGluR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Peripla_BP_I	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:2912	UniProtKB/Swiss-Prot
NCBI Gene	2912	ENTREZGENE
OMIM	604099	OMIM
PANTHER	METABOTROPIC GLUTAMATE RECEPTOR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	METABOTROPIC GLUTAMATE RECEPTOR 2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	7tm_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ANF_receptor	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NCD3G	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA28991	PharmGKB
PRINTS	GPCRMGR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MTABOTROPC2R	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MTABOTROPICR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F3_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F3_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F3_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F3_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF53822	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A8K1R9	ENTREZGENE, UniProtKB/TrEMBL
	B0AZM5	ENTREZGENE, UniProtKB/TrEMBL
	B0M0K7	ENTREZGENE
	C9JD41_HUMAN	UniProtKB/TrEMBL
	C9JL63_HUMAN	UniProtKB/TrEMBL
	GRM2_HUMAN	UniProtKB/Swiss-Prot
	H7BXL3	ENTREZGENE, UniProtKB/TrEMBL
	Q14416	ENTREZGENE
	Q14CU5	ENTREZGENE
	Q52MC6	ENTREZGENE
	Q86YG3	ENTREZGENE, UniProtKB/TrEMBL
	Q9H3N6	ENTREZGENE
UniProt Secondary	B0M0K7	UniProtKB/Swiss-Prot
	Q14CU5	UniProtKB/Swiss-Prot
	Q52MC6	UniProtKB/Swiss-Prot
	Q9H3N6	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-04-12	GRM2	glutamate metabotropic receptor 2	GRM2	glutamate receptor, metabotropic 2	Symbol and/or name change	5135510	APPROVED

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

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

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

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

Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)

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Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)