Ornithine aminotransferase

Preferred Label : Ornithine aminotransferase;

Symbol : OAT;

CISMeF acronym : OAT;

Type : Gene;

Alternative titles and symbols : Ornithine keto acid aminotransferase; Ornithine delta-aminotransferase; OKT;

Ensembl ID : ENSG00000065154;

Prefixed ID : *613349;

Details

Origin ID

613349;

UMLS CUI

C1417917;

Automatic exact mappings (from CISMeF team)
- Avena [MeSH Descriptor]
- Oat [NCIt concept]
- Thermoacoustic Computed Tomography [NCIt concept]
- oligoasthenoteratozoospermia [DO Concept]
- ornithine aminotransferase [ORDO Gene]
- ornithine aminotransferase [HGNC gene]
- ornithine-oxo-acid transaminase [MeSH Descriptor]
- ornithine-oxo-acid transaminase activity [GO term]
HGNC gene
- ornithine aminotransferase [HGNC gene]
NCIt concept(s)
- OAT Gene [NCIt concept]
- OAT wt Allele [NCIt concept]
- Ornithine Aminotransferase, Mitochondrial [NCIt concept]
ORDO concept(s)
- ornithine aminotransferase [ORDO Gene]
Phenotypes related
- Gyrate atrophy of choroid and retina [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OAT Gene [NCIt concept]
- ornithine aminotransferase [HGNC gene]

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