GSG1L
Description
The GSG1L (GSG1 like) is a protein-coding gene located on chromosome 16.
GSG1L is a subunit of the AMPA receptor (AMPAR) complex, specifically within the inner core. It plays a role in modifying the gating of AMPARs, influencing how these receptors open and close in response to neurotransmitters.
GSG1L is also known as PRO19651.
Associated Diseases
- schizophrenia 15
- Phelan-McDermid syndrome
- Potocki-Lupski syndrome
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- cancer
- joint contractures, osteochondromas, and B-cell lymphoma
- immunodeficiency 75
