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GRIN2C


Official Full Name
glutamate ionotropic receptor NMDA type subunit 2C
Organism
Homo sapiens
Gene ID
2905
Background
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
NR2C; GluN2C; NMDAR2C

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SHH104807 shRNA set against Mouse Grin2c(NM_010350.2) Inquiry
SHH104825 shRNA set against Human GRIN2C(NM_000835.3) Inquiry
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SHH307922 shRNA set against Human GRIN2C (NM_000835.3) Inquiry
SHH307926 shRNA set against Mouse GRIN2C (NM_010350.2) Inquiry
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CDFH008048 Human GRIN2C cDNA Clone(NM_000835.3) Inquiry
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MiUTR1M-05381 GRIN2C miRNA 3'UTR clone Inquiry
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CDCL114741 Human GRIN2C ORF clone (NM_000835.3) Inquiry
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