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NLGN3 gene

neuroligin 3

Key facts

Official symbol
NLGN3
Full name
NLGN3
Chromosome
X
Map location
Xq13.1
Organism
Homo sapiens
NCBI Gene ID
54413
Also known as
HNL3

Function summary

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. [provided by RefSeq, Oct 2009].

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Data source: NCBI Gene · alsesAI Gene Library