GRIK2: Difference between revisions
CSV import |
CSV import |
||
| Line 25: | Line 25: | ||
{{medicine-stub}} | {{medicine-stub}} | ||
{{No image}} | {{No image}} | ||
__NOINDEX__ | |||
Latest revision as of 13:17, 17 March 2025
GRIK2 or Glutamate Ionotropic Receptor Kainate Type Subunit 2 is a protein that in humans is encoded by the GRIK2 gene. It is a member of the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels.
Function[edit]
The protein encoded by the GRIK2 gene is a subunit of a kainate glutamate receptor. Glutamate receptors mediate the majority of excitatory neurotransmission in the brain. This receptor may have a role in synaptic plasticity, a process that underlies learning and memory. It is thought to interact with other proteins, like Neto1 and Neto2, to regulate kainate receptor function.
Clinical significance[edit]
Mutations in the GRIK2 gene have been associated with several neurological disorders, including autism, schizophrenia, and bipolar disorder. Studies have also suggested a potential role in the development and progression of Parkinson's disease.
Structure[edit]
The GRIK2 protein is a transmembrane protein, meaning it spans the membrane of the cells in which it is expressed. It is composed of several domains, including an extracellular domain, a transmembrane domain, and an intracellular domain. The extracellular domain is responsible for binding to glutamate, while the transmembrane domain forms the ion channel.
See also[edit]
References[edit]
<references />