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

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

Symbol : GRIN2B;

CISMeF acronym : GRIN2B;

Type : Gene;

Alternative titles and symbols : N-methyl-D-aspartate receptor channel, subunit epsilon-2; NMDAR2B; NR2B;

Ensembl ID : ENSG00000273079;

Prefixed ID : *138252;

Details

Origin ID

138252;

UMLS CUI

C1415300;

Automatic exact mappings (from CISMeF team)
- GRIN2B Gene [NCIt concept]
- GRIN2B wt Allele [NCIt concept]
- Glutamate Receptor Ionotropic, NMDA 2B [NCIt concept]
- glutamate ionotropic receptor NMDA type subunit 2B [HGNC gene]
- glutamate ionotropic receptor NMDA type subunit 2B [ORDO Gene]
HGNC gene
- glutamate ionotropic receptor NMDA type subunit 2B [HGNC gene]
NCIt concept(s)
- GRIN2B Gene [NCIt concept]
- GRIN2B wt Allele [NCIt concept]
- Glutamate Receptor Ionotropic, NMDA 2B [NCIt concept]
ORDO concept(s)
- glutamate ionotropic receptor NMDA type subunit 2B [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 27 [OMIM Phenotype]
- Intellectual developmental disorder, autosomal dominant 6, with or without seizures [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- GRIN2B Gene [NCIt concept]
- glutamate ionotropic receptor NMDA type subunit 2B [HGNC gene]

Keyword's position in hierarchy(ies) :

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