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]

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NLGN3
Identifiers
AliasesNLGN3, HNL3, neuroligin 3
External IDsOMIM: 300336; MGI: 2444609; HomoloGene: 23133; GeneCards: NLGN3; OMA:NLGN3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001166660
NM_018977
NM_181303
NM_001321276

NM_172932

RefSeq (protein)

NP_001160132
NP_001308205
NP_061850
NP_851820
NP_001160132.1

NP_766520

Location (UCSC)Chr X: 71.14 – 71.18 MbChr X: 100.34 – 100.37 Mb
PubMed search[3][4]
Wikidata
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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]

References

Further reading

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