MeSH Browser

MeSH Supplementary: prenyldiphosphate synthase, subunit 1, human
Unique ID: C519259
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C519259
Entry Term(s): PDSS1 protein, human; prenyl (decaprenyl) diphosphate synthase, subunit 1, human
Registry Numbers: EC 2.5.1.-
Heading Mapped to: *Alkyl and Aryl Transferases
Frequency: 6
Note: PDSS1 mutations in ubiquinone deficiency are involved in oxidative phosphorylation disorders; RefSeq NM_014317.3; NP_055132.2
Source: J Clin Invest 2007 Mar;117(3):765-72
Date of Entry: 2007/05/02
Revision Date: 1955/01/01

prenyldiphosphate synthase, subunit 1, human MeSH Supplementary Concept Data 2025