GRID1: Difference between revisions
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Latest revision as of 13:16, 17 March 2025
GRID1 or Glutamate Ionotropic Receptor Delta Type Subunit 1 is a protein that in humans is encoded by the GRID1 gene. It is a member of the glutamate receptor family, which plays an essential role in human neurological functions.
Function[edit]
GRID1 is a subunit of glutamate receptors, which are the predominant excitatory neurotransmitter receptors in the mammalian brain. These receptors are activated in a variety of normal neurophysiologic processes. This gene product belongs to the delta family of ionotropic glutamate receptors, which are sensitive to amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and to a lesser extent to kainate.
Clinical Significance[edit]
Mutations in the GRID1 gene have been associated with several neurological disorders, including schizophrenia and bipolar disorder. Studies have also suggested a potential link between GRID1 and susceptibility to epilepsy and Alzheimer's disease.
Structure[edit]
The GRID1 protein is a large, multi-domain protein that forms a tetramer to function as a glutamate receptor. It is composed of an extracellular N-terminal domain, a transmembrane domain, and an intracellular C-terminal domain. The N-terminal domain is responsible for ligand binding, while the transmembrane domain forms the ion channel.
See Also[edit]
References[edit]
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