- Gene Overview
- Interaction Network
- Sequence Verification
GRIN2C, glutamate ionotropic receptor NMDA type subunit 2C
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This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D), forming a channel that is permeable to calcium, potassium, and sodium, and whose properties are determined by subunit composition. Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease, Alzheimer's disease, depression, and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]
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Gene Synonyms (glutamate receptor ionotropic, NMDA 2C, N-methyl D-aspartate receptor subtype 2C, N-methyl-D-aspartate receptor subunit 2C, glutamate [NMDA] receptor subunit epsilon-3, glutamate receptor, ionotropic, N-methyl D-aspartate 2C, GluN2C, NMDAR2C, NR2C,)
- NCBI Gene ID:
2905
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>H0Y2V8
UNIPROT ID#>>Q8IW23
UNIPROT ID#>>O15398
UNIPROT ID#>>Q14957
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
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glutamate ionotropic receptor NMDA type subunit 2C interacts with:
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this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see
how a sequence matches to an experimentally-validated ORF clone.
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