GRIN2A: Difference between revisions
CSV import |
CSV import |
||
| Line 25: | Line 25: | ||
{{medicine-stub}} | {{medicine-stub}} | ||
{{No image}} | {{No image}} | ||
__NOINDEX__ | |||
Latest revision as of 13:35, 17 March 2025
GRIN2A is a gene that provides instructions for making a protein that is involved in the transmission of chemical signals in the brain. This protein is a part of NMDA receptors, which play a crucial role in normal brain development, synaptic plasticity, learning, and memory.
Function[edit]
The protein produced by the GRIN2A gene is a subunit of N-methyl-D-aspartate (NMDA) receptors. These receptors are channels that allow ions to flow through the neuron's cell membrane when activated. They are essential for the proper functioning of synaptic transmission, the process by which nerve cells communicate with each other.
Clinical significance[edit]
Mutations in the GRIN2A gene have been associated with a variety of neurological disorders, including epilepsy, speech disorders, and intellectual disability. These mutations can alter the function of NMDA receptors, disrupting the normal flow of ions into neurons and affecting the normal communication between nerve cells.
Research[edit]
Research is ongoing to better understand the role of the GRIN2A gene and its associated protein in brain function and development. This research may lead to new treatments for neurological disorders associated with mutations in this gene.
See also[edit]
References[edit]
<references />

