XB-GENEPAGE-494199
???displayGene.symbol???:
grin1
???displayGene.name???:
glutamate ionotropic receptor NMDA type subunit 1
???displayGene.synonyms???
LOC108699855
,
nmda1
,
nmdar1
(
Nomenclature history )
???displayGene.geneFunction???
glutamate receptor channel component
AI Protein Function
:
grin1 encodes the NMDA‑type glutamate receptor subunit NR1, a ligand‑gated ion channel that forms membrane‑bound receptors localized to the plasma membrane and postsynaptic density; it mediates calcium...[+]
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
autosomal dominant intellectual developmental disorder
MIM:
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES,
External Links:
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