NTNG1 wt Allele

Preferred Label : NTNG1 wt Allele;

NCIt synonyms : UNQ571/PRO1133; YLSR571; LMNT1; Netrin G1 wt Allele; Axon Guidance Molecule Gene; KIAA0976;

NCIt definition : Human NTNG1 wild-type allele is located in the vicinity of 1p13.3 and is approximately 343 kb in length. This allele, which encodes netrin-G1 protein, plays a role in neurite outgrowth.;

NCIt note : Mutation of the NTNG1 gene may be associated with autism. (Nature. 2012; 485:246-250.);

GenBank Accession Number : AB023193;

Details

Origin ID

C102456;

UMLS CUI

C3539669;

Automatic exact mappings (from CISMeF team)
- Netrin g1 [OMIM gene]
- netrin G1 [ORDO Gene]
OMIM relation
- Netrin g1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 1p13.3 [NCIt concept]
gene_is_element_in_pathway
- Axon Guidance Pathway [NCIt concept]
- Cell Adhesion Molecule Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Neural Development [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

Keyword's position in hierarchy(ies) :

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