Glutamate receptor, ionotropic, n-methyl-D-aspartate, subunit 1

Preferred Label : Glutamate receptor, ionotropic, n-methyl-D-aspartate, subunit 1;

Symbol : GRIN1;

CISMeF acronym : GRIN1;

Type : Gene;

Alternative titles and symbols : N-methyl-D-aspartate receptor channel, subunit zeta-1; NMDAR1; NR1;

Ensembl ID : ENSG00000176884;

Prefixed ID : *138249;

Détails

Origin ID

138249;

UMLS CUI

C1415298;

Automatic exact mappings (from CISMeF team)
- G protein regulated inducer of neurite outgrowth 1 [HGNC gene]
- NADPH-Dependent Diflavin Oxidoreductase 1 [NCIt concept]
- NDOR1 wt Allele [NCIt concept]
- NMDA receptor A1 [MeSH Supplementary Concept]
- glutamate ionotropic receptor NMDA type subunit 1 [HGNC gene]
- glutamate ionotropic receptor NMDA type subunit 1 [ORDO Gene]
HGNC gene
- glutamate ionotropic receptor NMDA type subunit 1 [HGNC gene]
NCIt concept(s)
- GRIN1 Gene [NCIt concept]
- GRIN1 wt Allele [NCIt concept]
- Glutamate Receptor Ionotropic, NMDA 1 [NCIt concept]
ORDO concept(s)
- glutamate ionotropic receptor NMDA type subunit 1 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 101 [OMIM Phenotype]
- Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant [OMIM Phenotype]
- Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- glutamate ionotropic receptor NMDA type subunit 1 [HGNC gene]

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