OAT wt Allele - CISMeF

Preferred Label : OAT wt Allele;

NCIt synonyms : OATASE; Gyrate Atrophy Gene; OKT; Ornithine Aminotransferase wt Allele; Ornithine Aminotransferase Precursor Gene; HOGA; GACR;

NCIt definition : Human OAT wild-type allele is located in the vicinity of 10q26.13 and is approximately 22 kb in length. This allele, which encodes ornithine aminotransferase, mitochondrial protein, is involved in the reversible transamination of ornithine to glutamate semialdehyde. Mutations in the gene are associated with gyrate atrophy.;

NCI Metathesaurus CUI : CL1926376;

GenBank Accession Number : BC016928;

Details

Origin ID

C204105;

UMLS CUI

C5890969;

OMIM relation
- Ornithine aminotransferase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 10q26.13 [NCIt concept]
gene_is_element_in_pathway
- Arginine and Proline Metabolism Pathway [NCIt concept]
gene_plays_role_in_process
- Amino Acid Biosynthesis [NCIt concept]
- Biogenic Amine Metabolic Process [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients