IDE wt Allele - CISMeF

Preferred Label : IDE wt Allele;

NCIt synonyms : Insulin-Degrading Enzyme wt Allele; INSULYSIN; RP11-366I13.1;

NCIt definition : Human IDE wild-type allele is located within 10q23-q25 and is approximately 122 kb in length. This allele, which encodes insulin-degrading enzyme protein, plays a role in the degradation of insulin and other bioactive peptides.;

GenBank Accession Number : M21188;

Details

Origin ID

C112877;

UMLS CUI

C3814868;

Automatic exact mappings (from CISMeF team)
- Insulin-degrading enzyme [OMIM gene]
- Insulysin (substance) [SNOMED CT concept]
- insulin degrading enzyme [HGNC gene]
- insulysin [MeSH Descriptor]
- insulysin [MeSH concept]
OMIM relation
- Insulin-degrading enzyme [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_is_element_in_pathway
- Alzheimer's Disease Pathway KEGG [NCIt concept]
gene_plays_role_in_process
- Hydrolysis [NCIt concept]
- Peptide Metabolism [NCIt concept]
- Proteolysis [NCIt concept]
- Proteolytic Processing [NCIt concept]

Keyword's position in hierarchy(ies) :

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