NLGN1 (Neuroligin 1) is a Protein Coding gene. Diseases associated with NLGN1 include Epilepsy, Familial Temporal Lobe, 3 and Corneal Granular Dystrophy. Among its related pathways are Ectoderm Differentiation and Cell adhesion molecules (CAMs). NLGN1 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.
