Glutamate receptor, ionotropic, n-methyl-D-aspartate, subunit 2a

Preferred Label : Glutamate receptor, ionotropic, n-methyl-D-aspartate, subunit 2a;

Symbol : GRIN2A;

CISMeF acronym : GRIN2A;

Type : Gene;

Alternative titles and symbols : N-methyl-D-aspartate receptor channel, subunit epsilon-1; NMDAR2A; NR2A;

Ensembl ID : ENSG00000183454;

Prefixed ID : *138253;

Details

Origin ID

138253;

UMLS CUI

C1415299;

Automatic exact mappings (from CISMeF team)
- GRIN2A Gene [NCIt concept]
- GRIN2A wt Allele [NCIt concept]
- Glutamate Receptor Ionotropic, NMDA 2A [NCIt concept]
- glutamate ionotropic receptor NMDA type subunit 2A [HGNC gene]
- glutamate ionotropic receptor NMDA type subunit 2A [ORDO Gene]
HGNC gene
- glutamate ionotropic receptor NMDA type subunit 2A [HGNC gene]
NCIt concept(s)
- GRIN2A Gene [NCIt concept]
- GRIN2A wt Allele [NCIt concept]
- Glutamate Receptor Ionotropic, NMDA 2A [NCIt concept]
ORDO concept(s)
- glutamate ionotropic receptor NMDA type subunit 2A [ORDO Gene]
Phenotypes related
- Epilepsy, focal, with speech disorder and with or without impaired intellectual development [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- GRIN2A Gene [NCIt concept]
- glutamate ionotropic receptor NMDA type subunit 2A [HGNC gene]

Keyword's position in hierarchy(ies) :

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