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NLGN4X gene

neuroligin 4 X-linked

Key facts

Official symbol
NLGN4X
Full name
NLGN4X
Chromosome
X
Map location
Xp22.32-p22.31
Organism
Homo sapiens
NCBI Gene ID
57502
Also known as
ASPGX2, AUTSX2, HLNX, HNL4X, NLGN4

Function summary

This gene encodes a member of the type-B carboxylesterase/lipase protein family. The encoded protein belongs to 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. The encoded protein interacts with discs large homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013].

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Data source: NCBI Gene · alsesAI Gene Library