NCBI Description of NLGN3
|This gene encodes a member of a family of neuronal cell surface proteins. Members of this family 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 and Asperger syndrome. Multiple transcript variants encoding distinct isoforms have been identified for this gene.|
Community Annotation of NLGN3 Add / Edit NLGN3: Annotations
No community annotations yet for NLGN3.
• "Mouse over" a mutation to see details.
Click on a tumor type to see its full list of significant genes.