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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 and axon. 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

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	Binge Drinking		ISO	Grm2 (Rattus norvegicus)	405100715	associated with human immunodeficiency virus infectious disease more ...	RGD
GRM2	Human	Cocaine-Related Disorders		ISO	Grm2 (Rattus norvegicus)	38501064	knockout compared to wild type	RGD
GRM2	Human	heroin dependence		ISO	Grm2 (Rattus norvegicus)	38501063		RGD
GRM2	Human	schizophrenia		ISO	Grm2 (Rattus norvegicus)	401901203	mRNA:decreased expression:prefrontal cortex and striatum	RGD

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	amphetamine abuse		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:20211215
GRM2	Human	schizophrenia		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:18923069
GRM2	Human	substance-induced psychosis		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:20211215
GRM2	Human	temporal lobe epilepsy		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:18804094

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	(+)-pilocarpine	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Pilocarpine results in decreased expression of GRM2 mRNA and Pilocarpine results in decreased expression of GRM2 protein	CTD	PMID:16793029 more ...
GRM2	Human	(S)-nicotine	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	Nicotine affects the expression of GRM2 mRNA	CTD	PMID:28339662
GRM2	Human	17beta-estradiol	increases activity	ISO	Grm2 (Rattus norvegicus)	6480464	Estradiol results in increased activity of GRM2 protein	CTD	PMID:15901789
GRM2	Human	2,3',4,4',5-Pentachlorobiphenyl	increases expression	ISO	Grm2 (Mus musculus)	6480464	2 more ...	CTD	PMID:31388691
GRM2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases methylation	ISO	Grm2 (Mus musculus)	6480464	Tetrachlorodibenzodioxin results in increased methylation of GRM2 gene	CTD	PMID:21212295
GRM2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of GRM2 mRNA	CTD	PMID:33387578
GRM2	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in decreased expression of GRM2 mRNA	CTD	PMID:32109520
GRM2	Human	2,3,7,8-Tetrachlorodibenzofuran	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	2 more ...	CTD	PMID:32109520
GRM2	Human	4,4'-sulfonyldiphenol	decreases expression	ISO	Grm2 (Mus musculus)	6480464	bisphenol S results in decreased expression of GRM2 mRNA	CTD	PMID:30951980
GRM2	Human	4,4'-sulfonyldiphenol	multiple interactions	ISO	Grm2 (Rattus norvegicus)	6480464	[bisphenol A co-treated with bisphenol F co-treated with bisphenol S] results in decreased expression of GRM2 mRNA	CTD	PMID:36041667
GRM2	Human	4-amino-2,6-dinitrotoluene	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	4-amino-2 and 6-dinitrotoluene affects the expression of GRM2 mRNA	CTD	PMID:21346803
GRM2	Human	6-propyl-2-thiouracil	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Propylthiouracil results in decreased expression of GRM2 mRNA	CTD	PMID:24780913
GRM2	Human	acrylamide	decreases expression	EXP		6480464	Acrylamide results in decreased expression of GRM2 mRNA	CTD	PMID:32763439
GRM2	Human	aflatoxin B1	decreases expression	EXP		6480464	Aflatoxin B1 results in decreased expression of GRM2 mRNA	CTD	PMID:22100608
GRM2	Human	amiodarone	increases expression	EXP		6480464	Amiodarone results in increased expression of GRM2 mRNA	CTD	PMID:19774075
GRM2	Human	ammonium chloride	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	Ammonium Chloride affects the expression of GRM2 mRNA	CTD	PMID:16483693
GRM2	Human	aristolochic acid A	increases expression	EXP		6480464	aristolochic acid I results in increased expression of GRM2 mRNA	CTD	PMID:33212167
GRM2	Human	arsane	affects methylation	EXP		6480464	Arsenic affects the methylation of GRM2 gene	CTD	PMID:25304211
GRM2	Human	arsenic atom	affects methylation	EXP		6480464	Arsenic affects the methylation of GRM2 gene	CTD	PMID:25304211
GRM2	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of GRM2 5' UTR	CTD	PMID:27901495
GRM2	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of GRM2 3' UTR more ...	CTD	PMID:27901495
GRM2	Human	bis(2-ethylhexyl) phthalate	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Diethylhexyl Phthalate results in decreased expression of GRM2 mRNA	CTD	PMID:15620428
GRM2	Human	bisphenol A	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of GRM2 mRNA	CTD	PMID:25181051 more ...
GRM2	Human	bisphenol A	multiple interactions	ISO	Grm2 (Rattus norvegicus)	6480464	[bisphenol A co-treated with bisphenol F co-treated with bisphenol S] results in decreased expression of GRM2 mRNA	CTD	PMID:36041667
GRM2	Human	bisphenol A	decreases expression	ISO	Grm2 (Mus musculus)	6480464	bisphenol A results in decreased expression of GRM2 mRNA	CTD	PMID:30951980
GRM2	Human	bisphenol F	decreases expression	ISO	Grm2 (Mus musculus)	6480464	bisphenol F results in decreased expression of GRM2 mRNA	CTD	PMID:30951980 and PMID:36706583
GRM2	Human	bisphenol F	multiple interactions	ISO	Grm2 (Rattus norvegicus)	6480464	[bisphenol A co-treated with bisphenol F co-treated with bisphenol S] results in decreased expression of GRM2 mRNA	CTD	PMID:36041667
GRM2	Human	carbamazepine	affects expression	EXP		6480464	Carbamazepine affects the expression of GRM2 mRNA	CTD	PMID:25979313
GRM2	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to GRM2 gene]	CTD	PMID:28238834
GRM2	Human	chaetocin	multiple interactions	ISO	Grm2 (Rattus norvegicus)	6480464	chaetocin affects the reaction [Dronabinol affects the expression of GRM2 mRNA]	CTD	PMID:29022873 and PMID:29481316
GRM2	Human	chlordecone	multiple interactions	ISO	Grm2 (Mus musculus)	6480464	Chlordecone promotes the reaction [Biomarkers metabolite binds to GRM2 gene]	CTD	PMID:31084621
GRM2	Human	chlorpyrifos	increases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Chlorpyrifos results in increased expression of GRM2 mRNA	CTD	PMID:17452286
GRM2	Human	cocaine	increases activity	ISO	Grm2 (Rattus norvegicus)	6480464	Cocaine results in increased activity of GRM2 protein	CTD	PMID:20416862
GRM2	Human	cocaine	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	Cocaine affects the expression of GRM2 protein	CTD	PMID:19105975
GRM2	Human	cocaine	decreases activity	ISO	Grm2 (Rattus norvegicus)	6480464	Cocaine results in decreased activity of GRM2 protein	CTD	PMID:18673447
GRM2	Human	curcumin	decreases expression	ISO	Grm2 (Mus musculus)	6480464	Curcumin results in decreased expression of GRM2 protein	CTD	PMID:25406541
GRM2	Human	diazinon	increases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Diazinon results in increased expression of GRM2 mRNA	CTD	PMID:17452286
GRM2	Human	entinostat	decreases expression	EXP		6480464	entinostat results in decreased expression of GRM2 mRNA	CTD	PMID:27188386
GRM2	Human	epoxiconazole	decreases expression	ISO	Grm2 (Mus musculus)	6480464	epoxiconazole results in decreased expression of GRM2 mRNA	CTD	PMID:35436446
GRM2	Human	ethanol	affects expression	ISO	Grm2 (Mus musculus)	6480464	Ethanol affects the expression of GRM2 mRNA	CTD	PMID:30319688
GRM2	Human	ethanol	increases expression	ISO	Grm2 (Mus musculus)	6480464	Ethanol results in increased expression of GRM2 mRNA	CTD	PMID:30319688
GRM2	Human	ethylparaben	decreases expression	EXP		6480464	ethyl-p-hydroxybenzoate results in decreased expression of GRM2 mRNA	CTD	PMID:37690743
GRM2	Human	fonofos	increases methylation	EXP		6480464	Fonofos results in increased methylation of GRM2 promoter	CTD	PMID:22847954
GRM2	Human	haloperidol	increases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Haloperidol results in increased expression of GRM2 mRNA	CTD	PMID:18923069
GRM2	Human	mescaline	multiple interactions	ISO	Grm2 (Mus musculus)	6480464	[Piperidines results in increased activity of GRM2 protein] which results in decreased susceptibility to Mescaline	CTD	PMID:21366332
GRM2	Human	methamphetamine	increases response to substance	EXP		6480464	GRM2 gene SNP results in increased susceptibility to Methamphetamine	CTD	PMID:20211215
GRM2	Human	methamphetamine	multiple interactions	ISO	Grm2 (Mus musculus)	6480464	[Piperidines results in increased activity of GRM2 protein] which results in decreased susceptibility to Methamphetamine	CTD	PMID:21366332
GRM2	Human	methylisothiazolinone	increases expression	EXP		6480464	2-methyl-4-isothiazolin-3-one results in increased expression of GRM2 mRNA	CTD	PMID:31629900
GRM2	Human	N-acetyl-L-cysteine	increases activity	EXP		6480464	Acetylcysteine results in increased activity of GRM2 protein	CTD	PMID:19136971
GRM2	Human	nicotine	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	Nicotine affects the expression of GRM2 mRNA	CTD	PMID:28339662
GRM2	Human	Nonylphenol	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	nonylphenol results in decreased expression of GRM2 mRNA	CTD	PMID:15620428
GRM2	Human	paraquat	affects expression	ISO	Grm2 (Rattus norvegicus)	6480464	Paraquat affects the expression of GRM2 mRNA	CTD	PMID:15206577
GRM2	Human	parathion	increases methylation	EXP		6480464	Parathion results in increased methylation of GRM2 promoter	CTD	PMID:22847954
GRM2	Human	permethrin	increases expression	EXP		6480464	Permethrin results in increased expression of GRM2 mRNA	CTD	PMID:37047231
GRM2	Human	piperidines	multiple interactions	ISO	Grm2 (Mus musculus)	6480464	[Piperidines results in increased activity of GRM2 protein] which results in decreased susceptibility to Mescaline and [Piperidines results in increased activity of GRM2 protein] which results in decreased susceptibility to Methamphetamine	CTD	PMID:21366332
GRM2	Human	rotenone	decreases expression	EXP		6480464	Rotenone results in decreased expression of GRM2 mRNA	CTD	PMID:29955902
GRM2	Human	sodium arsenite	decreases expression	ISO	Grm2 (Mus musculus)	6480464	sodium arsenite results in decreased expression of GRM2 protein	CTD	PMID:29748927
GRM2	Human	sodium fluoride	multiple interactions	ISO	Grm2 (Mus musculus)	6480464	[Sodium Fluoride results in increased abundance of Fluorides] which results in decreased expression of GRM2 mRNA	CTD	PMID:29187078
GRM2	Human	Soman	decreases expression	ISO	Grm2 (Rattus norvegicus)	6480464	Soman results in decreased expression of GRM2 mRNA	CTD	PMID:19281266
GRM2	Human	terbufos	increases methylation	EXP		6480464	terbufos results in increased methylation of GRM2 promoter	CTD	PMID:22847954
GRM2	Human	titanium dioxide	decreases expression	ISO	Grm2 (Mus musculus)	6480464	titanium dioxide results in decreased expression of GRM2 mRNA and titanium dioxide results in decreased expression of GRM2 protein	CTD	PMID:25411160
GRM2	Human	titanium dioxide	increases methylation	ISO	Grm2 (Mus musculus)	6480464	titanium dioxide results in increased methylation of GRM2 gene	CTD	PMID:35295148
GRM2	Human	titanium dioxide	decreases methylation	ISO	Grm2 (Mus musculus)	6480464	titanium dioxide results in decreased methylation of GRM2 gene	CTD	PMID:35295148
GRM2	Human	triclosan	increases expression	EXP		6480464	Triclosan results in increased expression of GRM2 mRNA	CTD	PMID:30510588
GRM2	Human	triptonide	increases expression	ISO	Grm2 (Mus musculus)	6480464	triptonide results in increased expression of GRM2 mRNA	CTD	PMID:33045310
GRM2	Human	tunicamycin	increases expression	ISO	Grm2 (Mus musculus)	6480464	Tunicamycin results in increased expression of GRM2 mRNA	CTD	PMID:17127020
GRM2	Human	valproic acid	affects expression	ISO	Grm2 (Mus musculus)	6480464	Valproic Acid affects the expression of GRM2 mRNA	CTD	PMID:17963808

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	adenylate cyclase-inhibiting G protein-coupled glutamate receptor signaling pathway	involved_in	IEA	GO:0001641	150520179		GOC	GO_REF:0000108
GRM2	Human	behavioral response to nicotine		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:28700935 and REF_RGD_ID:38501064
GRM2	Human	behavioral response to nicotine	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	cellular response to stress	acts_upstream_of_or_within	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	chemical synaptic transmission	involved_in	TAS		150520179	PMID:7620613	PINC	PMID:7620613
GRM2	Human	G protein-coupled glutamate receptor signaling pathway	involved_in	IBA	FB:FBgn0019985 more ...	150520179		GO_Central	GO_REF:0000033
GRM2	Human	G protein-coupled glutamate receptor signaling pathway	involved_in	IDA		150520179	PMID:37286794	UniProt	PMID:37286794
GRM2	Human	G protein-coupled receptor signaling pathway	involved_in	IEA	InterPro:IPR000162 more ...	150520179		InterPro	GO_REF:0000002
GRM2	Human	G protein-coupled receptor signaling pathway	involved_in	IEA	UniProtKB-KW:KW-0297	150520179		UniProt	GO_REF:0000043
GRM2	Human	gene expression	acts_upstream_of_or_within	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	glutamate receptor signaling pathway	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	glutamate secretion	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	intracellular glutamate homeostasis	acts_upstream_of_or_within	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	long-term synaptic depression	acts_upstream_of_or_within	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	negative regulation of adenylate cyclase activity	involved_in	TAS		150520179	PMID:7620613	PINC	PMID:7620613
GRM2	Human	positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction	involved_in	ISS	UniProtKB:P31421	150520179		ARUK-UCL	GO_REF:0000024
GRM2	Human	presynaptic modulation of chemical synaptic transmission	involved_in	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	regulation of dopamine secretion		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:30283001 and REF_RGD_ID:38501063
GRM2	Human	regulation of dopamine secretion	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	regulation of glutamate secretion		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:28700935 more ...
GRM2	Human	regulation of glutamate secretion	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	regulation of response to drug		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:28700935 more ...
GRM2	Human	regulation of response to drug	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	regulation of synaptic transmission, glutamatergic	involved_in	IBA	FB:FBgn0019985 more ...	150520179		GO_Central	GO_REF:0000033
GRM2	Human	response to cocaine		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:28700935 and REF_RGD_ID:38501064
GRM2	Human	response to cocaine	involved_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	signal transduction	involved_in	IEA	UniProtKB-KW:KW-0807	150520179		UniProt	GO_REF:0000043

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	astrocyte projection	located_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	astrocyte projection	located_in	ISS	UniProtKB:P31421	150520179		ARUK-UCL	GO_REF:0000024
GRM2	Human	axon	located_in	ISS	UniProtKB:P31421	150520179		ARUK-UCL	GO_REF:0000024
GRM2	Human	axon	located_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	cell projection	located_in	IEA	UniProtKB-KW:KW-0966	150520179		UniProt	GO_REF:0000043
GRM2	Human	dendrite	located_in	IEA	UniProtKB-SubCell:SL-0283	150520179		UniProt	GO_REF:0000044
GRM2	Human	glutamatergic synapse	is_active_in	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	membrane	located_in	IEA	InterPro:IPR000162 more ...	150520179		InterPro	GO_REF:0000002
GRM2	Human	membrane	located_in	IEA	UniProtKB-SubCell:SL-0162	150520179		UniProt	GO_REF:0000044
GRM2	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
GRM2	Human	neuron projection	located_in	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	plasma membrane	located_in	IEA	UniProtKB-KW:KW-1003	150520179		UniProt	GO_REF:0000043
GRM2	Human	plasma membrane	is_active_in	IDA		150520179	PMID:12011465	UniProt	PMID:12011465
GRM2	Human	plasma membrane	located_in	TAS		150520179	PMID:7620613	Reactome	PMID:7620613 more ...
GRM2	Human	plasma membrane	is_active_in	IBA	FB:FBgn0000206 more ...	150520179		GO_Central	GO_REF:0000033
GRM2	Human	plasma membrane	located_in	IEA	UniProtKB-SubCell:SL-0039	150520179		UniProt	GO_REF:0000044
GRM2	Human	postsynaptic membrane	is_active_in	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	presynaptic membrane	is_active_in	ISO	Grm2 (Rattus norvegicus)	9068941	PMID:35511883	SynGO	PMID:35511883 and REF_RGD_ID:405650215
GRM2	Human	presynaptic membrane	located_in	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	synapse	located_in	IEA	UniProtKB-KW:KW-0770	150520179		UniProt	GO_REF:0000043
GRM2	Human	synapse	located_in	IEA	UniProtKB-SubCell:SL-0258	150520179		UniProt	GO_REF:0000044

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	calcium channel regulator activity	enables	IEA	UniProtKB:Q14BI2 and ensembl:ENSMUSP00000023959	150520179		Ensembl	GO_REF:0000107
GRM2	Human	G protein-coupled receptor activity	enables	TAS		150520179	PMID:7620613	UniProt	PMID:7620613
GRM2	Human	G protein-coupled receptor activity	enables	IEA	ARBA:ARBA00029151	150520179		UniProt	GO_REF:0000117
GRM2	Human	G protein-coupled receptor activity	enables	IEA	UniProtKB-KW:KW-0297	150520179		UniProt	GO_REF:0000043
GRM2	Human	G protein-coupled receptor activity	enables	IEA	InterPro:IPR000337 more ...	150520179		InterPro	GO_REF:0000002
GRM2	Human	glutamate receptor activity	enables	TAS		150520179	PMID:7620613	UniProt	PMID:7620613
GRM2	Human	glutamate receptor activity	enables	IDA		150520179	PMID:37286794	UniProt	PMID:37286794
GRM2	Human	glutamate receptor activity	enables	IEA	ARBA:ARBA00029160	150520179		UniProt	GO_REF:0000117
GRM2	Human	group II metabotropic glutamate receptor activity		ISO	Grm2 (Rattus norvegicus)	9068941		RGD	PMID:12837619 and REF_RGD_ID:1298933
GRM2	Human	group II metabotropic glutamate receptor activity	enables	IBA	FB:FBgn0019985 more ...	150520179		GO_Central	GO_REF:0000033
GRM2	Human	group II metabotropic glutamate receptor activity	enables	IEA	UniProtKB:P31421 more ...	150520179		Ensembl	GO_REF:0000107
GRM2	Human	protein binding	enables	IPI	UniProtKB:P28223-1	150520179	PMID:18297054	IntAct	PMID:18297054
GRM2	Human	protein binding	enables	IPI	UniProtKB:P0DTC2 more ...	150520179	PMID:34903715	IntAct	PMID:34903715
GRM2	Human	protein binding	enables	IPI	UniProtKB:Q58DX5 and UniProtKB:Q9UMX0-2	150520179	PMID:25416956	IntAct	PMID:25416956
GRM2	Human	protein binding	enables	IPI	UniProtKB:O14880 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
GRM2	Human	scaffold protein binding	enables	IEA	UniProtKB:P31421 and ensembl:ENSRNOP00000017607	150520179		Ensembl	GO_REF:0000107
GRM2	Human	scaffold protein binding	enables	ISS	UniProtKB:P31421	150520179		ARUK-UCL	GO_REF:0000024

Imported Annotations - KEGG (archival)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
GRM2	Human	glutamate signaling pathway		IEA		6907045		KEGG	hsa:04724

#	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.

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

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 in GRM2
74 total 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
NM_000839.5(GRM2):c.643G>A (p.Asp215Asn)	single nucleotide variant	not specified [RCV004924773]	Chr3:51712665 [GRCh38] Chr3:51746681 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2006A>C (p.Gln669Pro)	single nucleotide variant	not specified [RCV004928402]	Chr3:51715779 [GRCh38] Chr3:51749795 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.817G>A (p.Glu273Lys)	single nucleotide variant	not specified [RCV004928403]	Chr3:51712839 [GRCh38] Chr3:51746855 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2080G>T (p.Val694Leu)	single nucleotide variant	not specified [RCV004928404]	Chr3:51715853 [GRCh38] Chr3:51749869 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1438C>G (p.Leu480Val)	single nucleotide variant	not specified [RCV004928405]	Chr3:51715211 [GRCh38] Chr3:51749227 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1684C>T (p.Arg562Cys)	single nucleotide variant	not specified [RCV004924774]	Chr3:51715457 [GRCh38] Chr3:51749473 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.781C>G (p.Pro261Ala)	single nucleotide variant	not specified [RCV004924776]	Chr3:51712803 [GRCh38] Chr3:51746819 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1727G>C (p.Cys576Ser)	single nucleotide variant	not specified [RCV004924777]	Chr3:51715500 [GRCh38] Chr3:51749516 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.289C>T (p.His97Tyr)	single nucleotide variant	not specified [RCV004928401]	Chr3:51709272 [GRCh38] Chr3:51743288 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1928T>C (p.Phe643Ser)	single nucleotide variant	not specified [RCV004928406]	Chr3:51715701 [GRCh38] Chr3:51749717 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1189C>T (p.Arg397Cys)	single nucleotide variant	not specified [RCV004924775]	Chr3:51713211 [GRCh38] Chr3:51747227 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2029G>A (p.Ala677Thr)	single nucleotide variant	not specified [RCV004928399]	Chr3:51715802 [GRCh38] Chr3:51749818 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.824C>T (p.Ala275Val)	single nucleotide variant	not specified [RCV004928400]	Chr3:51712846 [GRCh38] Chr3:51746862 [GRCh37] Chr3:3p21.2	uncertain significance

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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
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
597022473	GWAS1118547_H	macrophage inflammatory protein 1b measurement QTL GWAS1118547 (human)		5e-10	chemokine amount (VT:0008721)		3	51713272	51713273	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

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

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


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

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGAGCTGGGTCCCTTCGCATCTCTCTTCT
TGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGCTGCTTGCGCT
CCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCAGCAGAGGACT
GTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCTCGACAGTTGC
TCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATGCTCCCACTGC
CATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCT
ATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGC
ATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGC
CCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAG
GCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTC
TGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGC
GCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCC
CAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAA
GGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTG
CTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCC
GCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAG
CTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTA
CTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCC
AGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTG
GCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGC
ATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCC
TCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAAT
GGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACT
GCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTG
TAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAG
CCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCT
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
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGC
AGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGC
TCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGAT
GGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTC
AGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACG
AATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGC
CTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCAT
GACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCG
GTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGC
ACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTT
CAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTAC
AGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACC
AGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACC
CCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTT
ACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGC
AAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTA
CTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAA

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

GAGCGCAGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGAGCTGGGTCCCTTCGCATCTCTCTTCT
TGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGCTGCTTGCGCT
CCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCAGCAGAGGACT
GTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCTCGACAGTTGC
TCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATGCTCCCACTGC
CATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCT
ATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGC
ATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGC
CCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAG
GCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTC
TGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGC
GCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGGTGACCTGAAAG
TCTCCTGAAATCAAAAGTTATTTTAATAAGAGTGCCAGCTTTAAGAGAAATGACTGCTGCAGATCATCACTATGCTTCAGGAAGAATCACCGTGGGAACAGTGGGAGACAAAGCTTGGAAGCCCTGGC
CCAGGGTTAAGATGAAGACCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTAT
CGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGT
GAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTG
GCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCC
ACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCT
TGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGG
TGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAAC
CACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCAC
CATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCT
GCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCT
GGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTC
CAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGG
AGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAG
TCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTA
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
ACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGT
GCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCC
CTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGC
CCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTC
TTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGT
GTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCA
TCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTG
GTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGC
CAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCG
GCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCC
AGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAAC
CTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAG
TCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCT
GAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGC
CCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAA

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

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCGCCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCCAGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTCCTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTGCCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGA
GGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGCCCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTT
CCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAAATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCA
GGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAAGAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTC
ACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCTTGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTT
GCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGCTTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTG
GAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTTCTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTC
CAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAGAGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCC
CACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGACAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGG
CTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGGTTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCA
TCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGC
TGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCA
GCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCT
CGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATG
CTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGC
TTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCT
CTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCC
GCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTC
ATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCC
CTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGG
GACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGT
GTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAA
CCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGC
TGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCG
CTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCAC
CTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGG
TTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACA
ACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTAT
GTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGG
CCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTT
TTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAA
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
TCGGGGAGGCCTGGCCACTCCATCCACTGCTGGGAGTGGATTATCTGTCCTGCTAATCCCAGACACTGGAGGTGGCTAGGCAGCTGTCATGCTAGTCTCAGTCACTGGAGGTGGCTAGGCAGCTGTCC
TGCTAGTCCCAGTCACTGGAGGTGGCTAGGCAGCAGCCTGGGAAGATGTGGCTGTGCTAGCATCTATTTCTGCAGCCCCGGGTTGGGGCAGGGATGAGTGGGCGGCCTCCTACCTGCTGCTGTCTTCC
AGGGCCTCTGCTGAAGTTTTCTCCACAGTCCTCCTTAGGGCTCATGCATTTATCTCCAGAAGTCCAGTTACCTCCTTGCCATCCCAAGCTGCCTGCCTCCTGGATCAGGGCCCACGCCTCAGCAGTGG
TCTGCTTCTCCCTCGTCCTGATCAACACGAGGCTAGCCTGTCATCCGTAGGCTGCACCTGCCTGTTAATATTCCCCCTCATGGCTGCTCCTTCTCTCTTGCCCATGTCCCTATCATCTTCCCTTTGCC
AGGCACTGTGGCCTCCCATGCATTATCGTTTTTATCCTCTCAGCAGCCTTGTAGGGCAGGAATGTGAAACTGAGGCTCAGGGAGATTTGCCAACTCCAGGGGCCCAAAGGTGGCCAACCTCTTGAGGC
TATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTC
CGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGG
CCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCC
TCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTT
GCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGT
GCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAG
TTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATC
TTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTC
TCGCTGCAGTGAGCCCTGCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTG
GCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTC
TTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAA
GCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCC
AGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCC
GAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGA
AAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGT
CAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCT
GCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACA
GCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCT
CTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCC
TGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGT
TATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTGTCCTGTGGTTTATTTTGTATTACCTGTAAATAAAGTGGCTTTATTTTAAAAAATCA

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

AGAGCCAGCGAGCCAGCGAGCGAGCGAGCGGGAGCCGGAGCCTCGCGCCCCCCGCTCCACTCCGATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCG
CTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCGCCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGG
CGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCCAGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTC
GCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTCCTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTT
CAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTGCCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGA
GGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGCCCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTT
CCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAAATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCA
GGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAAGAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTC
ACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCTTGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTT
GCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGCTTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTG
GAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTTCTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTC
CAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAGAGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCC
CACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGACAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGG
CTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGGTTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCA
TCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGC
TGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCA
GCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCT
CGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATG
CTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGAC
AAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGG
CGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGA
AGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGT
GTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTT
CCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCA
TGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGCC
CCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGTGAGCCCT
GCCTCCAGAATGAGGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGAT

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

CCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGGTGACCTGAAAGTCTCCTGAAATCAAAAGTTATTTTAATA
AGAGTGCCAGCTTTAAGAGAAATGACTGCTGCAGATCATCACTATGCTTCAGGAAGAATCACCGTGGGAACAGTGGGAGACAAAGCTTGGAAGCCCTGGCCCAGGCCCCCTTTCGCCCAGCTGACACC
CACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGAAGTGAGCCCTGCCTCCAGAATGAGGTGAAGA
GTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGACTGGCTGC
TTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAATGCCACACC
AGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCGTCTTGGTT
TGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCACAGGTGGCC
ATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGCAACCACCG
CGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTTCACCATGT
ACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTGGCTGCCTC
TTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGGTCTGGCTC
CCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCACGTCCAGGG
CCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCCAGGAGCCT
CTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCCCAGTCCTA
ACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACAGTAGTTTG
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
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCGCTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGGCGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTCGCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTTCAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGAGCTGGGTCCCTTCGCATCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTAATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCAT
CCCCTTTGGGGCCATGGGATCGCTGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGTGCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCC
CAGTGCACCAGAAGGGCGGCCCAGCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTGCACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGC
GTGCGCCTGGGTGCACACATCCTCGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTCAGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGG
CTCTTATGCGACCCATGGTGATGCTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAACCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCT
CTACCAGTGCCAAGCTGAGTGACAAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGGCTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACT
GTGGCGTCTGAGGGCGACTATGGCGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCGGAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGG
TGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGCCAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTG
ATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCATCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGG
AACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCTCTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTT
TGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGCGATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTG
TGCTCAACGTCAAGTTTGATGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGC
TATCGCTACCAGAAGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTCGCTGCAGTGAGCCCTGCCTCCAGAATGA
GGTGAAGAGTGTGCAGCCGGGCGAAGTCTGCTGCTGGCTCTGCATTCCGTGCCAGCCCTATGAGTACCGATTGGACGAATTCACTTGCGCTGATTGTGGCCTGGGCTACTGGCCCAATGCCAGCCTGA
CTGGCTGCTTCGAACTGCCCCAGGAGTACATCCGCTGGGGCGATGCCTGGGCTGTGGGACCTGTCACCATCGCCTGCCTCGGTGCCCTGGCCACCCTCTTTGTGCTGGGTGTCTTTGTGCGGCACAAT
GCCACACCAGTGGTCAAGGCCTCAGGTCGGGAGCTCTGCTACATCCTGCTGGGTGGTGTCTTCCTCTGCTACTGCATGACCTTCATCTTCATTGCCAAGCCATCCACGGCAGTGTGTACCTTACGGCG
TCTTGGTTTGGGCACTGCCTTCTCTGTCTGCTACTCAGCCCTGCTCACCAAGACCAACCGCATTGCACGCATCTTCGGTGGGGCCCGGGAGGGTGCCCAGCGGCCACGCTTCATCAGTCCTGCCTCAC
AGGTGGCCATCTGCCTGGCACTTATCTCGGGCCAGCTGCTCATCGTGGTCGCCTGGCTGGTGGTGGAGGCACCGGGCACAGGCAAGGAGACAGCCCCCGAACGGCGGGAGGTGGTGACACTGCGCTGC
AACCACCGCGATGCAAGTATGTTGGGCTCGCTGGCCTACAATGTGCTCCTCATCGCGCTCTGCACGCTTTATGCCTTCAAGACTCGCAAGTGCCCCGAAAACTTCAACGAGGCCAAGTTCATTGGCTT
CACCATGTACACCACCTGCATCATCTGGCTGGCATTCCTGCCCATCTTCTATGTCACCTCCAGTGACTACCGGGTACAGACCACCACCATGTGCGTGTCAGTCAGCCTCAGCGGCTCCGTGGTGCTTG
GCTGCCTCTTTGCGCCCAAGCTGCACATCATCCTCTTCCAGCCGCAGAAGAACGTGGTTAGCCACCGGGCACCCACCAGCCGCTTTGGCAGTGCTGCTGCCAGGGCCAGCTCCAGCCTTGGCCAAGGG
TCTGGCTCCCAGTTTGTCCCCACTGTTTGCAATGGCCGTGAGGTGGTGGACTCGACAACGTCATCGCTTTGAAGACCCCATACTCCCGCCCTGACACAGCTGCTCCTGGGAACCTAGTGCAGACCCAC
GTCCAGGGCCAGGAGGAAGTTGGCTGGAGCACTGCAATAATTTATTACCCACCCTATGTCTGCCCCCAAAGTCACTTACCCACCTCCTTACCCCAGCTCTTCAGACTCAGAAGTCAGGAGCCTTGGCC
AGGAGCCTCTGCAGTGGCCACTAACTGCCCTTGTAGCTGTGTTTCCTCCTGGCCAGGCCCAGGGCTCAGAGAGGAGCAAGCCAGGGTTCACTCTGCCCTGGACCCGGGTGGCTGAGGACGGCAGGCCC
CAGTCCTAACCAGCAAAGGTGCTTCCAGCCCAGCCCCTCCCCCCAACTAGGGCCTTTTTTATTTTTTATATAAGTTACTCTGGGATGGGGAGGGTGGTTATTGTGGGGGCTGCCCCTCCCCCTGCACA
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
ATTCTCTCCGCGCCAGAGCCAGCGCGCCAGGTAGGGTGAGCCGGTGGTGGTGGTGCCGCTGCCGCTGCCGACCTTTTTGGCCCTTACCTCACGTCCCAGGGTCCTGCGGGCCCTCAAGTTGTGGGGCG
CCCGCGCTGCTGTGTCCAGACAGCGTTCCCTGAGAGCTCCGGGAAGCGGGAAGACAGCCCCGGGCGTCCCGCCTTTCTTCTCCAGAAAACGCACGCCCCACATCGCACTCCCCCGTTCCTCCTGCTCC
AGCGTCCTCTGGTCCTTCTTTCTGTCTGTGCCTCCGTCTTTGTCTCAACCTCTCAGGCTTGCTCGCTCCCTGCCCAGATTTTGTGGCCCAGGCTCCTGGCTGTCTGACTCCGGGTTTCTGTCCCCTTC
CTGCCTCTGAGCTTCCGTCTGGGCCTCCCCTCTGGGAGACTTGCGACTTGACCAGTTTTGGCTTCAGCCCCCATCTGGGTCCCTGTCTCCATCTGTGCTGGTCTTCCTCCCTGCTTCTCCCTCGCTTG
CCTGGGTAAGCTGCTGCTTTCCTGATCCCCAGAGGAGCCCAGTGCCCCTGCCCTGGGGAGCTGAGGGGGCAAAATGAAGAGGCTCAGCCTCCGTGGCCAGCACATGGGGTCCTTGAGTTAGTTGCTGC
CCTTCTTCAAACTCAGTTTCCTTTCCTGTTCTGAGGAAAGAGGTATGTCCCTCTCCCAGCCTTTCCAAGCCTGTGTGATTGTGAGAGCCTTTGTGGGGTGTGTGTTTGGGAAGGCAACTGGGGTACAA
ATGATTGGACGCAGTGGGGAAGAGACAGGGAGGGGGTCTCTGAGGGCCATGGCTAGGGTGGGCAGGGCCCTGAAGCTGAGGATGGGGAGATTGGAAATGGTGACTTTCTCTGCTGGGTCGGGAGTGAA
GAGAAAACAGAGGCACAAAATCTCAAGCAGTGTTCTACACAGAGCTAGAGAGTCCCGCACTCTCACCCTCAGCACTGTTTGGAGACTCTAGCCCCCAACCCTGACACACACATACGTGAACATCTGCT
TGCCCTGTTGACTTAGGACCTTGAGCCACTTGGGTACCCTCCCTGAGGCCAGCCATTCCACCTTGCTGTCTCATTCCCAGGGCTTAGTGTCTCTATTCCTTCCTCAGTCAGCAAACTGTGGGGATGGC
TTTTTAAGAACCAAAGGTTAGAACCCTTGGGTGTTCACATGGGCTCCAGTCTCCCCACGGGTTGGAGACTGTCCCTTAGAGATGCTTCCCTTCCTCTTCCCTGGTGGGTCCTGAGACAGCAGTTCCTT
CTCTCTGGAAATCCAAGGCTCAGGATGGGGACCTCTGAGTTTGTGACTGTGACATAGTCTGTTCCAAAGGTATTGACCTCGGGGTCCTGGGAGGTTTGTGCTGTTCTTGGACACCCTTTGAATTACAG
AGGGGTCAGCATTGGCTGGGGTCTCCTGTCCTCTGCCTGGGACTTCACTGCTTGCATCTCTCCCCACTGCTGAGTTTGGTAGGGGAATATGGCCCATCTCTCACCAAGCTGAGGCCAGGGCTGAGAGA
CAGGTCCAGGGGAGTCCCAGGAGCTTCTCAACCTACTTAATGACACCATCCTGTCCCTCCCTGGCTTTTGAGTACCTAGGAAAGGGGCTCGTGGGGAGGCAGAGTCAGAAGGGGCAGCTGCTCTCAGG
TTCCACTTTTCCTGGTCTGTTTTTCTGTCTTTCTATCTCTCTGCAGGAGCTGGGTCCCTTCGCATCTCTCTTCTTGTCTGTCCTTTCCTGGTCCCTGTTTCCTCCTCTCTTTGCCTTCGCTGCTTCTA
ATCTCATCCCCTGGAGACCCAGGTCTGCGGGACCCATCCATCCCCTTTGGGGCCATGGGATCGCTGCTTGCGCTCCTGGCACTGCTGCTGCTGTGGGGTGCTGTGGCTGAGGGCCCAGCCAAGAAGGT
GCTGACCCTGGAGGGAGACTTGGTGCTGGGTGGGCTGTTCCCAGTGCACCAGAAGGGCGGCCCAGCAGAGGACTGTGGTCCTGTCAATGAGCACCGTGGCATCCAGCGCCTGGAGGCCATGCTTTTTG
CACTGGACCGCATCAACCGTGACCCGCACCTGCTGCCTGGCGTGCGCCTGGGTGCACACATCCTCGACAGTTGCTCCAAGGACACACATGCGCTGGAGCAGGCACTGGACTTTGTGCGTGCCTCACTC
AGCCGTGGTGCTGATGGCTCACGCCACATCTGCCCCGACGGCTCTTATGCGACCCATGGTGATGCTCCCACTGCCATCACTGGTGTTATTGGCGGTTCCTACAGTGATGTCTCCATCCAGGTGGCCAA
CCTCTTGAGGCTATTTCAGATCCCACAGATTAGCTACGCCTCTACCAGTGCCAAGCTGAGTGACAAGTCCCGCTATGACTACTTTGCCCGCACAGTGCCTCCTGACTTCTTCCAAGCCAAGGCCATGG
CTGAGATTCTCCGCTTCTTCAACTGGACCTATGTGTCCACTGTGGCGTCTGAGGGCGACTATGGCGAGACAGGCATTGAGGCCTTTGAGCTAGAGGCTCGTGCCCGCAACATCTGTGTGGCCACCTCG
GAGAAAGTGGGCCGTGCCATGAGCCGCGCGGCCTTTGAGGGTGTGGTGCGAGCCCTGCTGCAGAAGCCCAGTGCCCGCGTGGCTGTCCTGTTCACCCGTTCTGAGGATGCCCGGGAGCTGCTTGCTGC
CAGCCAGCGCCTCAATGCCAGCTTCACCTGGGTGGCCAGTGATGGTTGGGGGGCCCTGGAGAGTGTGGTGGCAGGCAGTGAGGGGGCTGCTGAGGGTGCTATCACCATCGAGCTGGCCTCCTACCCCA
TCAGTGACTTTGCCTCCTACTTCCAGAGCCTGGACCCTTGGAACAACAGCCGGAACCCCTGGTTCCGTGAATTCTGGGAGCAGAGGTTCCGCTGCAGCTTCCGGCAGCGAGACTGCGCAGCCCACTCT
CTCCGGGCTGTGCCCTTTGAGCAGGAGTCCAAGATCATGTTTGTGGTCAATGCAGTGTACGCCATGGCCCATGCGCTCCACAACATGCACCGTGCCCTCTGCCCCAACACCACCCGGCTCTGTGACGC
GATGCGGCCAGTTAACGGGCGCCGCCTCTACAAGGACTTTGTGCTCAACGTCAAGTTTGATGGTGACCTGAAAGTCTCCTGAAATCAAAAGTTATTTTAATAAGAGTGCCAGCTTTAAGAGAAATGAC
TGCTGCAGATCATCACTATGCTTCAGGAAGAATCACCGTGGGAACAGTGGGAGACAAAGCTTGGAAGCCCTGGCCCAGGGTTAAGATGAAGAGTACTTCCAATAGAACTGACATTCAGAGTTAGCTAC
AATCAGTGTAGGGGTTAGGGTTGGAATCTGGGGTCCGATTTGGTTGATGTTAGAGCAAGGCTAAATTCAGCATGTTTGGCTTGGGTGGAATTTATGGTAGGGCTAGAGTTGGATTTTGAGAACTTTTA
GGCTGAGTAGAAAGAGTAGGTGCTTGAGGGGACCTGGGTTTGAATCTAGGCTGCACTATTCACTCATGGGGCCTTAAGCATGTCTTCTGCTTTCTTGAACCCTGATTTCTCACTGGGGCCAGGGATGG
CTGTAAATCCTGGCTAGAGCCTGGCTGGGAGATGTGAGGTTTACAGGGGATGAAGTGGGGGTGGAGAGAGGAAGTGATTTTCCAGCCACTGACCACATTCTGGTGAATGGCAGTGGTTGCAGGTGACC
AGTGAGGTTGGGATTCAGTTTGCACCAGGATGACTGTTAGGACTAGGGGTGCTGGAGCTGGGGTTGTTGTTAGGATTAGTGGGGACAGGATTGGAGCTGAGACTGGGTTTAGCCTTAGCATTGAGTTT
GGGGAGAGGGCTGTAGTGTATGTTTCGATGAAGTTGGGATTTGGAGCCTGGGTTGGAAAGTGTTGGATAGTACTAAAGTTGAATTTGGGGAGTCATGGTTGGGGATTGATGTGGGCATTAGGTTTTTG
GAGATGTCTGGGCTTTAAGGCTGGGATTACATTTGGCATTTAGGGTTGGGGTTTGATGTTGGAGTTTAGGAGTAAGACTTTGTTGTCATCTCTCATTTAGAAAAATGATTGGGGTCAAGGCAGGATTT
AGTATTGGGTTAAGGATTGGAAGGGCTAATGGTGGTCTTAGCTCTGGCATTTGGGTTCCATGTTAGGGTGAATGTTGAGGTCACATCAGGGTAACACACTAGTCCAACCTTCTCTTCCTTCCCTCCCC
CATCCTAGCCCCCTTTCGCCCAGCTGACACCCACAATGAGGTCCGCTTTGACCGCTTTGGTGATGGTATTGGCCGCTACAACATCTTCACCTATCTGCGTGCAGGCAGTGGGCGCTATCGCTACCAGA
AGGTGGGCTACTGGGCAGAAGGCTTGACTCTGGACACCAGCCTCATCCCATGGGCCTCACCCTCAGCCGGCCCCCTGCCCGCCTCTC

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 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
	ENSP00000378492
	ENSP00000378492.3
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 MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEAMLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQAKAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELASYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSV QPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLG TAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYT TCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL hide sequence

RefSeq Acc Id:

XP_011531938 ⟸ XM_011533636

- Peptide Label:

isoform X3

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEAMLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT
HGDAPTAITGVIGGSYSDVSIQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTH
NEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDA
WAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIV
VAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQ
KNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531944 ⟸ XM_011533642

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA
MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYATHGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA
KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRALLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA
SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGD
GIGRYNIFTYLRAGSGRYRYQK

hide sequence

RefSeq Acc Id:

XP_011531939 ⟸ XM_011533637

- Peptide Label:

isoform X4

- Sequence:

show sequence

MAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRALL
QKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELASYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNAVY
AMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQP
GEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTA
FSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTC
IIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531945 ⟸ XM_011533643

- Peptide Label:

isoform X6

- Sequence:

show sequence

MTAADHHYASGRITVGTVGDKAWKPWPRPPFAQLTPTMRSALTALVMVLAATTSSPICVQAVGAIATRSEPCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEY
IRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALIS
GQLLIVVAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHI
ILFQPQKNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

Protein Domains

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

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

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

Database	Acc Id	Source(s)
COSMIC	GRM2	COSMIC
Ensembl Genes	ENSG00000164082	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000296479	ENTREZGENE
	ENST00000395052	ENTREZGENE
	ENST00000395052.8	UniProtKB/Swiss-Prot
	ENST00000475478	ENTREZGENE
Gene3D-CATH	2.10.50.30	UniProtKB/Swiss-Prot
	3.40.50.2300	UniProtKB/Swiss-Prot
GTEx	ENSG00000164082	GTEx
HGNC ID	HGNC:4594	ENTREZGENE
Human Proteome Map	GRM2	Human Proteome Map
InterPro	ANF_lig-bd_rcpt	UniProtKB/Swiss-Prot
	GPCR_3	UniProtKB/Swiss-Prot
	GPCR_3_9-Cys_dom	UniProtKB/Swiss-Prot
	GPCR_3_9-Cys_sf	UniProtKB/Swiss-Prot
	GPCR_3_C	UniProtKB/Swiss-Prot
	GPCR_3_CS	UniProtKB/Swiss-Prot
	GPCR_3_mtglu_rcpt	UniProtKB/Swiss-Prot
	GPCR_3_mtglu_rcpt_2	UniProtKB/Swiss-Prot
	mGluR	UniProtKB/Swiss-Prot
	Peripla_BP_I	UniProtKB/Swiss-Prot
KEGG Report	hsa:2912	UniProtKB/Swiss-Prot
NCBI Gene	2912	ENTREZGENE
OMIM	604099	OMIM
PANTHER	METABOTROPIC GLUTAMATE RECEPTOR	UniProtKB/Swiss-Prot
Pfam	7tm_3	UniProtKB/Swiss-Prot
	ANF_receptor	UniProtKB/Swiss-Prot
	NCD3G	UniProtKB/Swiss-Prot
PharmGKB	PA28991	PharmGKB
PRINTS	GPCRMGR	UniProtKB/Swiss-Prot
	MTABOTROPC2R	UniProtKB/Swiss-Prot
	MTABOTROPICR	UniProtKB/Swiss-Prot
PROSITE	G_PROTEIN_RECEP_F3_1	UniProtKB/Swiss-Prot
	G_PROTEIN_RECEP_F3_2	UniProtKB/Swiss-Prot
	G_PROTEIN_RECEP_F3_3	UniProtKB/Swiss-Prot
	G_PROTEIN_RECEP_F3_4	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF53822	UniProtKB/Swiss-Prot
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) unavailable


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)