prenyldiphosphate synthase, subunit 1, human

Preferred Label : prenyldiphosphate synthase, subunit 1, human;

MeSH note : PDSS1 mutations in ubiquinone deficiency are involved in oxidative phosphorylation disorders; RefSeq NM_014317.3; NP_055132.2;

MeSH synonym : PDSS1 protein, human; prenyl (decaprenyl) diphosphate synthase, subunit 1, human;

Registry Number MeSH : EC 2.5.1.-;

Is substance : O;

Details

Origin ID

C519259;

UMLS CUI

C1956528;

MeSH term(s) associated for indexing
- alkyl and aryl transferases [MeSH Descriptor]
Record concept(s)
- prenyldiphosphate synthase, subunit 1, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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