Homo sapiens Gene: GRIN2C | |||||||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||||||
InnateDB Gene | IDBG-67631.6 | ||||||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||||||
Gene Symbol | GRIN2C | ||||||||||||||||||||||||||||
Gene Name | glutamate receptor, ionotropic, N-methyl D-aspartate 2C | ||||||||||||||||||||||||||||
Synonyms | GluN2C; NMDAR2C; NR2C | ||||||||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||||||||
Ensembl Gene | ENSG00000161509 | ||||||||||||||||||||||||||||
Encoded Proteins |
glutamate receptor, ionotropic, N-methyl D-aspartate 2C
glutamate receptor, ionotropic, N-methyl D-aspartate 2C
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Protein Structure | |||||||||||||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||||||||
Entrez Gene | |||||||||||||||||||||||||||||
Summary |
N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. NMDA channel has been shown to be involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDA receptor channels are heteromers composed of the key receptor subunit NMDAR1 (GRIN1) and 1 or more of the 4 NMDAR2 subunits: NMDAR2A (GRIN2A), NMDAR2B (GRIN2B), NMDAR2C (GRIN2C), and NMDAR2D (GRIN2D). [provided by RefSeq, Mar 2010] 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 Information | |||||||||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||||||||
Genomic Location | Chromosome 17:74842023-74861504 | ||||||||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||||||||
Band | q25.1 | ||||||||||||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||||||||
REACTOME |
Ras activation uopn Ca2+ infux through NMDA receptor pathway
CREB phosphorylation through the activation of Ras pathway
CREB phosphorylation through the activation of CaMKII pathway
Unblocking of NMDA receptor, glutamate binding and activation pathway
Neuronal System pathway
Post NMDA receptor activation events pathway
Activation of NMDA receptor upon glutamate binding and postsynaptic events pathway
Transmission across Chemical Synapses pathway
Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell pathway
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KEGG |
Neuroactive ligand-receptor interaction pathway
Long-term potentiation pathway
Alzheimer's disease pathway
Calcium signaling pathway pathway
Amyotrophic lateral sclerosis (ALS) pathway
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INOH |
GPCR Dopamine D1like receptor signaling pathway pathway
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PID NCI | |||||||||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||||||||
SwissProt | |||||||||||||||||||||||||||||
TrEMBL | H0Y2V8 Q8IW23 | ||||||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||||||
Entrez Gene | 2905 | ||||||||||||||||||||||||||||
UniGene | Hs.436980 | ||||||||||||||||||||||||||||
RefSeq | NM_001278553 NM_000835 XM_006721845 XM_006721846 XM_006721847 | ||||||||||||||||||||||||||||
HUGO | HGNC:4587 | ||||||||||||||||||||||||||||
OMIM | 138254 | ||||||||||||||||||||||||||||
CCDS | CCDS62330 CCDS32724 | ||||||||||||||||||||||||||||
HPRD | 00699 | ||||||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||||||
EMBL | AC068874 BC041128 CH471099 | ||||||||||||||||||||||||||||
GenPept | AAH41128 EAW89202 | ||||||||||||||||||||||||||||
RNA Seq Atlas | 2905 | ||||||||||||||||||||||||||||