GRM2 (glutamate metabotropic receptor 2)

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Gene: GRM2 (glutamate metabotropic receptor 2) Homo sapiens

Analyze

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 and regulation of glutamatergic synaptic transmission. Predicted to act upstream of or within several processes, including intracellular glutamate homeostasis; long-term synaptic depression; and regulation of protein kinase B signaling. Predicted to be located in dendrite and presynaptic membrane. Predicted to be part of astrocyte projection and axon. Predicted to be active in glutamatergic synapse and plasma 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

Mouse

Rat

Chinchilla

Bonobo

Dog

Squirrel

Pig

Green Monkey

Naked Mole-Rat

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p13 Ensembl	3	51,707,068 - 51,718,613 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	51,741,084 - 51,752,629 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	51,718,004 - 51,727,669 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	51,718,037 - 51,727,168	NCBI
Celera	3	51,718,848 - 51,731,506 (+)	NCBI		Celera
Cytogenetic Map	3	p21.2	NCBI
HuRef	3	51,802,839 - 51,816,142 (+)	NCBI		HuRef
CHM1_1	3	51,693,893 - 51,705,447 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	51,738,578 - 51,751,605 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

amphetamine abuse (EXP)

Cocaine-Related Disorders (ISO)

genetic disease (IAGP)

heroin dependence (ISO)

schizophrenia (EXP)

substance-induced psychosis (EXP)

temporal lobe epilepsy (EXP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-pilocarpine (ISO)

(S)-nicotine (ISO)

17beta-estradiol (ISO)

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

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

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

4,4'-sulfonyldiphenol (ISO)

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

6-propyl-2-thiouracil (ISO)

acrylamide (EXP)

aflatoxin B1 (EXP)

amiodarone (EXP)

ammonium chloride (ISO)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (ISO)

bisphenol F (ISO)

carbamazepine (EXP)

CGP 52608 (EXP)

chaetocin (ISO)

chlordecone (ISO)

chlorpyrifos (ISO)

cocaine (ISO)

curcumin (ISO)

diazinon (ISO)

entinostat (EXP)

epoxiconazole (ISO)

ethanol (ISO)

fonofos (EXP)

haloperidol (ISO)

mescaline (ISO)

methamphetamine (EXP,ISO)

methylisothiazolinone (EXP)

N-acetyl-L-cysteine (EXP)

nicotine (ISO)

Nonylphenol (ISO)

paraquat (ISO)

parathion (EXP)

piperidines (ISO)

rotenone (EXP)

sodium arsenite (ISO)

sodium fluoride (ISO)

Soman (ISO)

terbufos (EXP)

titanium dioxide (ISO)

triclosan (EXP)

triptonide (ISO)

tunicamycin (ISO)

valproic acid (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

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

behavioral response to nicotine (IEA,ISO)

cell communication (IEA)

chemical synaptic transmission (IEA,TAS)

G protein-coupled glutamate receptor signaling pathway (IBA)

G protein-coupled receptor signaling pathway (IEA)

gene expression (IEA,ISO)

glutamate secretion (IEA)

intracellular glutamate homeostasis (IEA,ISO)

long-term synaptic depression (IEA,ISO)

negative regulation of adenylate cyclase activity (TAS)

presynaptic modulation of chemical synaptic transmission (IEA)

regulation of dopamine secretion (IEA,ISO)

regulation of glutamate secretion (IEA,ISO)

regulation of protein kinase B signaling (IEA,ISS)

regulation of response to drug (IEA,ISO)

regulation of synaptic transmission, glutamatergic (IBA)

response to cocaine (IEA,ISO)

signal transduction (IEA)

signaling (IEA)

Cellular Component

astrocyte projection (IEA,ISS)

axon (IEA,ISS)

cell projection (IEA)

dendrite (IEA)

glutamatergic synapse (IEA,ISO)

membrane (IEA)

neuron projection (IEA)

obsolete integral component of postsynaptic membrane (IEA)

plasma membrane (IBA,IEA)

plasma membrane (IEA,TAS)

plasma membrane (TAS)

presynapse (ISO)

presynaptic membrane (IEA)

synapse (IEA)

Molecular Function

adenylate cyclase inhibiting G protein-coupled glutamate receptor activity (IBA)

calcium channel regulator activity (IEA)

G protein-coupled receptor activity (IEA,TAS)

glutamate receptor activity (IEA,TAS)

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

protein binding (IPI)

scaffold protein binding (IEA,ISS)

Molecular Pathway Annotations Click to see Annotation Detail View

glutamate signaling pathway (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	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.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	Online Mendelian Inheritance in Man, OMIM (TM).	Online Mendelian Inheritance in Man, OMIM (TM).
4.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
5.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
7.	Deletion of Type 2 Metabotropic Glutamate Receptor Decreases Sensitivity to Cocaine Reward in Rats.	Yang HJ, etal., Cell Rep. 2017 Jul 11;20(2):319-332. doi: 10.1016/j.celrep.2017.06.046.

Additional References at PubMed

PMID:7620613	PMID:8824806	PMID:8863838	PMID:9651375	PMID:11317221	PMID:11641422	PMID:11840499	PMID:11850456	PMID:11891216	PMID:11897108	PMID:12477932	PMID:15035981
PMID:15246118	PMID:15330338	PMID:15489334	PMID:15837331	PMID: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

Genomics

Comparative Map Data

GRM2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	51,707,068 - 51,718,613 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p13 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

Grm2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
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_SHRSP_BbbUtx_1.0	8	111,102,213 - 111,115,309 (-)	NCBI	Rnor_SHRSP
UTH_Rnor_WKY_Bbb_1.0	8	108,944,991 - 108,958,085 (-)	NCBI	Rnor_WKY
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
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
Mhudiblu_PPA_v0	3	51,639,792 - 51,652,779 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3

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	NW_004936529	3,042,220 - 3,053,670 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

GRM2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	13	33,926,804 - 33,938,269 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	33,924,303 - 33,938,279 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	13	37,130,553 - 37,141,351 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

GRM2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	22	13,044,974 - 13,056,469 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	22	13,046,641 - 13,056,453 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	153,898,374 - 153,910,372 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Grm2
(Heterocephalus glaber - naked mole-rat)

Naked Mole-rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624730	5,419,896 - 5,431,361 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624730	5,419,892 - 5,431,268 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in GRM2
11 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3p21.31-14.3(chr3:49461000-55314500)x1	copy number loss	See cases [RCV000051511]	Chr3:49461000..55314500 [GRCh38] Chr3:49498433..55348528 [GRCh37] Chr3:49473437..55323568 [NCBI36] Chr3:3p21.31-14.3	pathogenic
NM_000839.3(GRM2):c.1297C>T (p.Arg433Cys)	single nucleotide variant	Malignant melanoma [RCV000066134]	Chr3:51715070 [GRCh38] Chr3:51749086 [GRCh37] Chr3:51724126 [NCBI36] Chr3:3p21.2	not provided
GRCh38/hg38 3p21.2-14.3(chr3:51394434-55064449)x1	copy number loss	See cases [RCV000143631]	Chr3:51394434..55064449 [GRCh38] Chr3:51431865..55098476 [GRCh37] Chr3:51406905..55073516 [NCBI36] Chr3:3p21.2-14.3	likely pathogenic
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	Inborn genetic diseases [RCV002773009]	Chr3:51715268 [GRCh38] Chr3:51749284 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.374C>A (p.Ser125Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002906267]	Chr3:51709357 [GRCh38] Chr3:51743373 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1346G>A (p.Gly449Asp)	single nucleotide variant	Inborn genetic diseases [RCV002685316]	Chr3:51715119 [GRCh38] Chr3:51749135 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.130G>A (p.Gly44Ser)	single nucleotide variant	Inborn genetic diseases [RCV002728914]	Chr3:51709113 [GRCh38] Chr3:51743129 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1394G>A (p.Arg465His)	single nucleotide variant	Inborn genetic diseases [RCV002946332]	Chr3:51715167 [GRCh38] Chr3:51749183 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1066A>G (p.Ser356Gly)	single nucleotide variant	Inborn genetic diseases [RCV002684107]	Chr3:51713088 [GRCh38] Chr3:51747104 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1037G>A (p.Arg346His)	single nucleotide variant	Inborn genetic diseases [RCV002973546]	Chr3:51713059 [GRCh38] Chr3:51747075 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2363G>A (p.Arg788Gln)	single nucleotide variant	Inborn genetic diseases [RCV002980370]	Chr3:51716136 [GRCh38] Chr3:51750152 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.842C>T (p.Ala281Val)	single nucleotide variant	Inborn genetic diseases [RCV002782933]	Chr3:51712864 [GRCh38] Chr3:51746880 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.975T>A (p.Ser325Arg)	single nucleotide variant	Inborn genetic diseases [RCV002950491]	Chr3:51712997 [GRCh38] Chr3:51747013 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1709G>A (p.Gly570Glu)	single nucleotide variant	Inborn genetic diseases [RCV002803098]	Chr3:51715482 [GRCh38] Chr3:51749498 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1399C>T (p.Arg467Cys)	single nucleotide variant	Inborn genetic diseases [RCV002987239]	Chr3:51715172 [GRCh38] Chr3:51749188 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.133G>A (p.Gly45Ser)	single nucleotide variant	Inborn genetic diseases [RCV002698352]	Chr3:51709116 [GRCh38] Chr3:51743132 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2138G>A (p.Arg713Gln)	single nucleotide variant	Inborn genetic diseases [RCV002826703]	Chr3:51715911 [GRCh38] Chr3:51749927 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2460G>T (p.Gln820His)	single nucleotide variant	Inborn genetic diseases [RCV002916481]	Chr3:51717732 [GRCh38] Chr3:51751748 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1886C>T (p.Thr629Met)	single nucleotide variant	Inborn genetic diseases [RCV002744440]	Chr3:51715659 [GRCh38] Chr3:51749675 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1469C>T (p.Pro490Leu)	single nucleotide variant	Inborn genetic diseases [RCV002984020]	Chr3:51715242 [GRCh38] Chr3:51749258 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2491C>A (p.Pro831Thr)	single nucleotide variant	Inborn genetic diseases [RCV002850138]	Chr3:51717763 [GRCh38] Chr3:51751779 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1087G>A (p.Ala363Thr)	single nucleotide variant	Inborn genetic diseases [RCV002961231]	Chr3:51713109 [GRCh38] Chr3:51747125 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.97G>A (p.Val33Met)	single nucleotide variant	Inborn genetic diseases [RCV003008867]	Chr3:51709080 [GRCh38] Chr3:51743096 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.603C>G (p.Phe201Leu)	single nucleotide variant	Inborn genetic diseases [RCV002921834]	Chr3:51712625 [GRCh38] Chr3:51746641 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1612G>A (p.Ala538Thr)	single nucleotide variant	Inborn genetic diseases [RCV002655744]	Chr3:51715385 [GRCh38] Chr3:51749401 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.2171G>A (p.Arg724His)	single nucleotide variant	Inborn genetic diseases [RCV002678826]	Chr3:51715944 [GRCh38] Chr3:51749960 [GRCh37] Chr3:3p21.2	uncertain significance
NM_000839.5(GRM2):c.1592G>A (p.Arg531Gln)	single nucleotide variant	Inborn genetic diseases [RCV002655846]	Chr3:51715365 [GRCh38] Chr3:51749381 [GRCh37] Chr3:3p21.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2573
Count of miRNA genes:	957
Interacting mature miRNAs:	1155
Transcripts:	ENST00000296479, ENST00000395052, ENST00000419928, ENST00000442933, ENST00000464585, ENST00000475478, ENST00000477330, ENST00000496661
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

WI-20087

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

RH66405

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

A002C19

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

GRM2

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

SHGC-77001

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	3	p21.2	UniSTS
TNG Radiation Hybrid Map	3	32009.0	UniSTS
GeneMap99-GB4 RH Map	3	162.92	UniSTS
NCBI RH Map	3	494.1	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

High

Medium

403

314

Low

554

776

525

504

3125

642

2673

476

641

625

1916

Below cutoff

1798

2173

1093

443

1052

351

1148

1533

635

262

621

858

574

839

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_000839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001349116	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001349117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_146059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533636	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017006271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024453490	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448048	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448049	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
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

Reference Sequences

RefSeq Acc Id:

ENST00000296479 ⟹ ENSP00000296479

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,707,088 - 51,718,112 (+)	Ensembl

RefSeq Acc Id:

ENST00000395052 ⟹ ENSP00000378492

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,707,068 - 51,718,613 (+)	Ensembl

RefSeq Acc Id:

ENST00000419928 ⟹ ENSP00000404797

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,707,411 - 51,709,193 (+)	Ensembl

RefSeq Acc Id:

ENST00000442933 ⟹ ENSP00000408906

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,708,845 - 51,718,252 (+)	Ensembl

RefSeq Acc Id:

ENST00000464585

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,707,305 - 51,718,613 (+)	Ensembl

RefSeq Acc Id:

ENST00000475478

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,707,090 - 51,718,613 (+)	Ensembl

RefSeq Acc Id:

ENST00000477330

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,711,272 - 51,712,581 (+)	Ensembl

RefSeq Acc Id:

ENST00000496661

RefSeq Status:

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p13 Ensembl	3	51,711,272 - 51,714,068 (+)	Ensembl

RefSeq Acc Id:

NM_000839 ⟹ NP_000830

RefSeq Status:

REVIEWED

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

NM_001349116 ⟹ NP_001336045

RefSeq Status:

REVIEWED

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

NM_001349117 ⟹ NP_001336046

RefSeq Status:

REVIEWED

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

NR_146059

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_011533636 ⟹ XP_011531938

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_011533637 ⟹ XP_011531939

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_011533642 ⟹ XP_011531944

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_011533643 ⟹ XP_011531945

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_017006271 ⟹ XP_016861760

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_024453490 ⟹ XP_024309258

RefSeq Status:

Type:

CODING

Position:

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

Sequence:

show sequence

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

hide sequence

RefSeq Acc Id:

XM_047448047 ⟹ XP_047304003

RefSeq Status:

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

RefSeq Status:

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

RefSeq Status:

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

RefSeq Status:

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

RefSeq Status:

Type:

CODING

Position:

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

Protein Sequences


Protein RefSeqs	NP_000830	(Get FASTA)	NCBI Sequence Viewer
	NP_001336045	(Get FASTA)	NCBI Sequence Viewer
	NP_001336046	(Get FASTA)	NCBI Sequence Viewer
	XP_011531938	(Get FASTA)	NCBI Sequence Viewer
	XP_011531939	(Get FASTA)	NCBI Sequence Viewer
	XP_011531944	(Get FASTA)	NCBI Sequence Viewer
	XP_011531945	(Get FASTA)	NCBI Sequence Viewer
	XP_016861760	(Get FASTA)	NCBI Sequence Viewer
	XP_024309258	(Get FASTA)	NCBI Sequence Viewer
	XP_047304003	(Get FASTA)	NCBI Sequence Viewer
	XP_047304004	(Get FASTA)	NCBI Sequence Viewer
	XP_047304005	(Get FASTA)	NCBI Sequence Viewer
	XP_047304006	(Get FASTA)	NCBI Sequence Viewer
	XP_047304007	(Get FASTA)	NCBI Sequence Viewer
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
	Q14416	(Get FASTA)	NCBI Sequence Viewer

Reference Sequences

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

RefSeq Acc Id:

XP_011531938 ⟸ XM_011533636

- Peptide Label:

isoform X3

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA
MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT
HGDAPTAITGVIGGSYSDVSIQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQ
ESKIMFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTH
NEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSE
PCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDA
WAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTA
VCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIV
VAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNE
AKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQ
KNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531944 ⟸ XM_011533642

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRGIQRLEA
MLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHICPDGSYAT
HGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDYFARTVPPDFFQA
KAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRA
LLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELA
SYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNA
VYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGD
GIGRYNIFTYLRAGSGRYRYQK

hide sequence

RefSeq Acc Id:

XP_011531939 ⟸ XM_011533637

- Peptide Label:

isoform X4

- Sequence:

show sequence

MAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEKVGRAMSRAAFEGVVRALL
QKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWGALESVVAGSEGAAEGAITIELASY
PISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFRQRDCAAHSLRAVPFEQESKIMFVVNAVY
AMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVRFDRFGDGI
GRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQP
GEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLG
ALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTA
FSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTG
KETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTC
IIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSR
FGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

XP_011531945 ⟸ XM_011533643

- Peptide Label:

isoform X6

- Sequence:

show sequence

MTAADHHYASGRITVGTVGDKAWKPWPRPPFAQLTPTMRSALTALVMVLAATTSSPICVQAVGA
IATRSEPCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEY
IRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFI
AKPSTAVCTLRRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALIS
GQLLIVVAWLVVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKC
PENFNEAKFIGFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHI
ILFQPQKNVVSHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

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

RefSeq Acc Id:

NP_001336046 ⟸ NM_001349117

- Peptide Label:

isoform d

- Sequence:

show sequence

MTAADHHYASGRITVGTVGDKAWKPWPRVKMKTPFRPADTHNEVRFDRFGDGIGRYNIFTYLRA
GSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQNEVKSVQPGEVCCWLCIPC
QPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLGALATLFVLGVF
VRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTLRRLGLGTAFSVCYSALLTK
TNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWLVVEAPGTGKETAPERREVV
TLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTCIIWLAFLPIFY
VTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSRFGSAAARASSS
LGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

RefSeq Acc Id:

NP_001336045 ⟸ NM_001349116

- Peptide Label:

isoform c

- Sequence:

show sequence

MFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRLYKDFVLNVKFDAPFRPADTHNEVR
FDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTLDTSLIPWASPSAGPLPASRCSEPCLQ
NEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADCGLGYWPNASLTGCFELPQEYIRWGDAWAVG
PVTIACLGALATLFVLGVFVRHNATPVVKASGRELCYILLGGVFLCYCMTFIFIAKPSTAVCTL
RRLGLGTAFSVCYSALLTKTNRIARIFGGAREGAQRPRFISPASQVAICLALISGQLLIVVAWL
VVEAPGTGKETAPERREVVTLRCNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFI
GFTMYTTCIIWLAFLPIFYVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVV
SHRAPTSRFGSAAARASSSLGQGSGSQFVPTVCNGREVVDSTTSSL

hide sequence

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

RefSeq Acc Id:

ENSP00000296479 ⟸ ENST00000296479

RefSeq Acc Id:

ENSP00000408906 ⟸ ENST00000442933

RefSeq Acc Id:

ENSP00000404797 ⟸ ENST00000419928

RefSeq Acc Id:

ENSP00000378492 ⟸ ENST00000395052

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

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

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

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

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

Protein Domains

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

Protein Structures

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

Promoters

RGD ID:

6864566

Promoter ID:

EPDNEW_H5448

Type:

initiation region

Name:

GRM2_1

Description:

glutamate metabotropic receptor 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H5449

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

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

RGD ID:

6864568

Promoter ID:

EPDNEW_H5449

Type:

multiple initiation site

Name:

GRM2_2

Description:

glutamate metabotropic receptor 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H5448

Experiment Methods:

Single-end sequencing.

Position:

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

RGD ID:

6801106

Promoter ID:

HG_KWN:45181

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

NB4

Transcripts:

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

Position:

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

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:4594	AgrOrtholog
COSMIC	GRM2	COSMIC
Ensembl Genes	ENSG00000164082	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein	ENSP00000296479	ENTREZGENE
	ENSP00000296479.5	UniProtKB/TrEMBL
	ENSP00000378492	ENTREZGENE
	ENSP00000378492.3	UniProtKB/Swiss-Prot
	ENSP00000404797.1	UniProtKB/TrEMBL
	ENSP00000408906.2	UniProtKB/TrEMBL
Ensembl Transcript	ENST00000296479	ENTREZGENE
	ENST00000296479.9	UniProtKB/TrEMBL
	ENST00000395052	ENTREZGENE
	ENST00000395052.8	UniProtKB/Swiss-Prot
	ENST00000419928.1	UniProtKB/TrEMBL
	ENST00000442933.2	UniProtKB/TrEMBL
	ENST00000475478	ENTREZGENE
Gene3D-CATH	2.10.50.30	UniProtKB/Swiss-Prot
	3.40.50.2300	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000164082	GTEx
HGNC ID	HGNC:4594	ENTREZGENE
Human Proteome Map	GRM2	Human Proteome Map
InterPro	ANF_lig-bd_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_9-Cys_dom	UniProtKB/Swiss-Prot
	GPCR_3_9-Cys_sf	UniProtKB/Swiss-Prot
	GPCR_3_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_mtglu_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_3_mtglu_rcpt_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Peripla_BP_I	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:2912	UniProtKB/Swiss-Prot
NCBI Gene	2912	ENTREZGENE
OMIM	604099	OMIM
PANTHER	METABOTROPIC GLUTAMATE RECEPTOR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	METABOTROPIC GLUTAMATE RECEPTOR 2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	7tm_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ANF_receptor	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NCD3G	UniProtKB/Swiss-Prot
PharmGKB	PA28991	PharmGKB
PRINTS	GPCRMGR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MTABOTROPC2R	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MTABOTROPICR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F3_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F3_2	UniProtKB/Swiss-Prot
	G_PROTEIN_RECEP_F3_3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F3_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF53822	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	C9JD41_HUMAN	UniProtKB/TrEMBL
	C9JL63_HUMAN	UniProtKB/TrEMBL
	GRM2_HUMAN	UniProtKB/Swiss-Prot
	H7BXL3	ENTREZGENE, UniProtKB/TrEMBL
	Q14416	ENTREZGENE
	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

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

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Imported Annotations - KEGG (archival)