GRIN1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Glutamate [NMDA] receptor subunit zeta-1 is a protein that in humans is encoded by the GRIN1 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesGRIN1, GluN1, MRD8, NMDA1, NMDAR1, NR1, NMD-R1, glutamate ionotropic receptor NMDA type subunit 1, NDHMSR, NDHMSD, DEE101
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GRIN1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGRIN1, GluN1, MRD8, NMDA1, NMDAR1, NR1, NMD-R1, glutamate ionotropic receptor NMDA type subunit 1, NDHMSR, NDHMSD, DEE101
External IDsOMIM: 138249; MGI: 95819; HomoloGene: 7187; GeneCards: GRIN1; OMA:GRIN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000832
NM_001185090
NM_001185091
NM_007327
NM_021569

RefSeq (protein)

NP_000823
NP_001172019
NP_001172020
NP_015566
NP_067544

Location (UCSC)Chr 9: 137.14 – 137.17 MbChr 2: 25.18 – 25.21 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. The gene consists of 21 exons and is alternatively spliced, producing transcript variants differing in the C-terminus. The sequence of exon 5 is identical in vertebrates, with exon 5 splicing demonstrated in human, mouse and rat.[7][8][9][10] Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits.[6]

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