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GRIN2A, glutamate ionotropic receptor NMDA type subunit 2A

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GRIN2A, glutamate ionotropic receptor NMDA type subunit 2A

  • 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]

  • Gene Synonyms (glutamate receptor ionotropic, NMDA 2A, N-methyl D-aspartate receptor subtype 2A, N-methyl-D-aspartate receptor channel, subunit epsilon-1, N-methyl-D-aspartate receptor subunit 2A, glutamate receptor, ionotropic, N-methyl D-aspartate 2A, EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A,)
  • NCBI Gene ID: 2903
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q12879
    UNIPROT ID#>>Q547U9
    UNIPROT ID#>>Q59EW6
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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