NLGN3
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Neuroligin-3 is a protein that in humans is encoded by the NLGN3 gene.[5][6][7]
External IDsOMIM: 300336; MGI: 2444609; HomoloGene: 23133; GeneCards: NLGN3; OMA:NLGN3 - orthologs
This gene encodes a member of the neuroligin family of neuronal cell surface proteins. Neuroligins may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. Mutations in this gene may be associated with autism spectrum disorders (ASDs).[8][9] Multiple transcript variants encoding distinct isoforms have been identified for this gene, but their full length sequences have not been determined.[7]