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Gene : GRIN2C Homo sapiens

Name  ? glutamate ionotropic receptor NMDA type subunit 2C Cytological Location  17q25.1
Brief Description  glutamate ionotropic receptor NMDA type subunit 2C
Description  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]
  • synonyms:
  • NM_000835,
  • uc002jlt.3,
  • NMDAR2C,
  • NR2C,
  • glutamate receptor, ionotropic, N-methyl D-aspartate 2C,
  • HGNC:4587,
  • GRIN2C,
  • GluN2C,
  • GluN2C,
  • NMDAR2C,
  • OTTHUMG00000044524
  • identifiers:
  • 2905,
  • ENSG00000161509,
  • GRIN2C

Genome feature

Region: gene ? Length: 18823  
Location: 17:74842021-74860843 reverse strand Cyto location: 17q25.1


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3753 SN Ps

5 Cross References

16 Data Sets

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97 Rna Seq Results