ABHD5 protein, human

Preferred Label : ABHD5 protein, human;

MeSH note : mutations in ABHD5 gene cause Chanarin-Dorfman syndrome, RefSeq NM_016006;

MeSH synonym : CGI-58 protein, human; abhydrolase domain containing 5, human;

Registry Number MeSH : EC 3.1.-; EC 2.3.1.51;

Is substance : O;

UNII : EC 2.3.1.51;

Details

Origin ID

C439972;

UMLS CUI

C1099265;

Automatic exact mappings (from CISMeF team)
- Esterase [NCIt concept]
- Protein Artemis [NCIt concept]
MeSH term(s) associated for indexing
- 1-acylglycerol-3-phosphate o-acyltransferase [MeSH Descriptor]
Record concept(s)
- ABHD5 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients