phospholipase A2 group VI

Preferred Label : phospholipase A2 group VI;

Approved symbol HGNC : PLA2G6;

Name synonyms HGNC : neurodegeneration with brain iron accumulation 2;

Alias symbols HGNC : PARK14; iPLA2beta; PNPLA9; iPLA2; NBIA2;

Chromosome HGNC : 22q13.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000184381;

Details

Origin ID

HGNC:9039;

UMLS CUI

C1418624;

Automatic exact mappings (from CISMeF team)
- 85 kDa Calcium-Independent Phospholipase A2 [NCIt concept]
- Parkinson disease 14, autosomal recessive [OMIM Phenotype]
- Phospholipase a2, group VI [OMIM gene]
- group VI phospholipases A2 [MeSH Descriptor]
- group VI phospholipases A2 [MeSH concept]
- phospholipase A2 group VI [ORDO Gene]
NCIt concept
- PLA2G6 Gene [NCIt concept]
OMIM gene
- Phospholipase a2, group VI [OMIM gene]
Orphanet gene
- phospholipase A2 group VI [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PLA2G6 Gene [NCIt concept]
- Phospholipase a2, group VI [OMIM gene]

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