apolipoprotein C2

Preferred Label : apolipoprotein C2;

Approved symbol HGNC : APOC2;

Chromosome HGNC : 19q13.32;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000234906;

Details

Origin ID

HGNC:609;

UMLS CUI

C1412477;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein C-II [NCIt concept]
- Apolipoprotein C2 Measurement [NCIt concept]
- apolipoprotein c-ii [MeSH Descriptor]
Currated CISMeF NLP mapping
- APOC2 Gene [NCIt concept]
- Apolipoprotein C-ii [OMIM gene]
- apolipoprotein C2 [ORDO Gene]
NCIt concept
- APOC2 Gene [NCIt concept]
OMIM gene
- Apolipoprotein C-ii [OMIM gene]
Orphanet gene
- apolipoprotein C2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- APOC2 Gene [NCIt concept]
- Apolipoprotein C-ii [OMIM gene]

Keyword's position in hierarchy(ies) :

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