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GRIN2A gene

glutamate ionotropic receptor NMDA type subunit 2A

Key facts

Official symbol
GRIN2A
Full name
GRIN2A
Chromosome
16
Map location
16p13.2
Organism
Homo sapiens
NCBI Gene ID
2903
Also known as
EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A

Function summary

This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014].

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Data source: NCBI Gene · alsesAI Gene Library