neuroligin 3 - CISMeF

Preferred Label : neuroligin 3;

Approved symbol HGNC : NLGN3;

Alias symbols HGNC : ASPGX1; HNL3; KIAA1480; AUTSX1;

Chromosome HGNC : Xq13.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000196338;

Details

Origin ID

HGNC:14289;

UMLS CUI

C1422546;

Automatic exact mappings (from CISMeF team)
- Asperger syndrome, X-linked, susceptibility to, 1 [OMIM Phenotype]
- Autism, susceptibility to, X-linked 1 [OMIM Phenotype]
- Neuroligin 3 [ORDO Gene]
- Neuroligin 3 [OMIM gene]
- neuroligin 3 [MeSH Supplementary Concept]
- neuroligin 3 [MeSH concept]
OMIM gene
- Neuroligin 3 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuroligin 3 [OMIM gene]

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