NLGN4X wt Allele

Preferred Label : NLGN4X wt Allele;

NCIt synonyms : HLNX; NLGN4; AUTSX2; MGC22376; KIAA1260; ASPGX2; NLGN; HNLX; HNL4X; UNQ365/PRO701; NL4; Neuroligin 4 X-Linked wt Allele; Neuroligin 4, X-Linked Gene;

NCIt definition : Human NLGN4X wild-type allele is located within Xp22.32-p22.31 and is approximately 339 kb in length. This allele, which encodes neuroligin-4, X-linked protein, may be involved in the mediation of synapse function. Mutations in the gene are associated with X-linked autism and Asperger's syndrome.;

GenBank Accession Number : AB033086;

Details

Origin ID

C75746;

UMLS CUI

C2698413;

OMIM relation
- Neuroligin 4, X-linked [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_is_element_in_pathway
- Cell Adhesion Molecule Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Neural Development [NCIt concept]

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