GSG1L

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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