alanine--glyoxylate aminotransferase

Preferred Label : alanine--glyoxylate aminotransferase;

Approved symbol HGNC : AGXT;

Name synonyms HGNC : L-alanine: glyoxylate aminotransferase 1; glycolicaciduria; primary hyperoxaluria type 1; oxalosis I;

Alias symbols HGNC : SPT; PH1; AGXT1; AGT1; AGT; Ser-PyrAT; TLH6;

Chromosome HGNC : 2q37.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000172482;

Details

Origin ID

HGNC:341;

UMLS CUI

C1412290;

Automatic exact mappings (from CISMeF team)
- Alanine-glyoxylate aminotransferase [OMIM gene]
- Angiotensinogen [OMIM Phenotype]
- Hyperoxaluria, primary, type I [OMIM Phenotype]
- Primary hyperoxaluria type 1 [ICD-11 Sub-sub category]
- Primary hyperoxaluria type 1 [ORDO Disease]
- Primary hyperoxaluria type 1 [MeSH concept]
- alanine--glyoxylate aminotransferase [ORDO Gene]
- primary hyperoxaluria type 1 [MeSH Supplementary Concept]
- primary hyperoxaluria type 1 [DO Concept]
OMIM gene
- Alanine-glyoxylate aminotransferase [OMIM gene]
Orphanet gene
- alanine--glyoxylate aminotransferase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- AGXT gene [LOINC component]
- Alanine-glyoxylate aminotransferase [OMIM gene]

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