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Gene: GRIN2A (glutamate ionotropic receptor NMDA type subunit 2A) Homo sapiens
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Symbol: GRIN2A
Name: glutamate ionotropic receptor NMDA type subunit 2A
Description: Exhibits glutamate-gated calcium ion channel activity. Involved in calcium ion transmembrane import into cytosol and response to ethanol. Localizes to the NMDA selective glutamate receptor complex. Implicated in Huntington's disease; bipolar disorder; and schizophrenia. Biomarker of Alzheimer's disease and vascular dementia.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: EPND; FESD; GluN2A; glutamate [NMDA] receptor subunit epsilon-1; glutamate receptor ionotropic, NMDA 2A; glutamate receptor, ionotropic, N-methyl D-aspartate 2A; hNR2A; LKS; N-methyl D-aspartate receptor subtype 2A; N-methyl-D-aspartate receptor channel, subunit epsilon-1; N-methyl-D-aspartate receptor subunit 2A; NMDA receptor subtype 2A; NMDAR2A; NR2A; RP11-297M9.2
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38169,753,404 - 10,182,928 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37169,847,265 - 10,276,611 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36169,762,923 - 10,184,112 (-)NCBINCBI36hg18NCBI36
Build 34169,762,922 - 10,184,112NCBI
Celera1610,014,039 - 10,444,548 (-)NCBI
Cytogenetic Map16p13.2NCBI
HuRef1610,193,124 - 10,195,907 (-)NCBIHuRef
HuRef169,767,577 - 9,952,307 (-)NCBIHuRef
CHM1_1169,847,225 - 10,277,115 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
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