ATG16L1 wt Allele

Preferred Label : ATG16L1 wt Allele;

NCIt synonyms : APG16L; FLJ10035; UNQ9393/PRO34307; Autophagy Related 16-Like 1 (S. cerevisiae) wt Allele; ATG16L; hCG_1817841; ATG16 Autophagy Related 16-Like (S. cerevisiae) Gene; APG16L Beta; WDR30; APG16 Autophagy 16-Like (S. cerevisiae) Gene; ATG16A; IBD10; ATG16 Autophagy Related 16-Like 1 (S. cerevisiae) Gene;

NCIt definition : Human ATG16L1 wild-type allele is located in the vicinity of 2q37.1 and is approximately 86 kb in length. This allele, which encodes autophagy-related protein 16-1, is involved in the formation of autophagosomes. Mutation of the gene is associated with Crohn disease (inflammatory bowel disease 10).;

GenBank Accession Number : AK000897;

Details

Origin ID

C119724;

UMLS CUI

C3890435;

Automatic exact mappings (from CISMeF team)
- ATG16 autophagy related 16-like 1 (S. cerevisiae) [ORDO Gene]
- Autophagy 16-like 1 [OMIM gene]
- Inflammatory bowel disease (crohn disease) 10 [OMIM Phenotype]
- inflammatory bowel disease 10 [DO Concept]
OMIM relation
- Autophagy 16-like 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2q37.1 [NCIt concept]
gene_is_element_in_pathway
- Autophagy Regulation Pathway [NCIt concept]
gene_plays_role_in_process
- Autophagy [NCIt concept]
- Homodimerization [NCIt concept]

Keyword's position in hierarchy(ies) :

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