Prenyl diphosphate synthase, subunit 1

Preferred Label : Prenyl diphosphate synthase, subunit 1;

Symbol : PDSS1;

CISMeF acronym : PDSS1;

Type : Gene;

Alternative titles and symbols : Decaprenyl diphosphate synthase; Solanesyl diphosphate synthase, mouse, homolog of; Trans-prenyltransferase; Polyprenyl pyrophosphate synthetase; Coq1, s. cerevisiae, homolog of; DPS; SPS; TPT; COQ1;

Ensembl ID : ENSG00000148459;

Prefixed ID : *607429;

Details

Origin ID

607429;

UMLS CUI

C1843919;

Automatic exact mappings (from CISMeF team)
- 9 alpha,11 alpha,15 alpha-trihydroxy-16-phenoxy-17,18,19,20-tetranorprosta-4,5,13-trienoic acid [MeSH Supplementary Concept]
- Coxopodopatellar syndrome [ORDO Disease]
- Disintegration per Second [NCIt concept]
- Planned Time Point Name [NCIt concept]
- SHH wt Allele [NCIt concept]
- Stiff person spectrum disorder [ORDO Disease]
- TBX4 wt Allele [NCIt concept]
- decaprenyl diphosphate synthase subunit 1 [ORDO Gene]
- decaprenyl diphosphate synthase subunit 1 [HGNC gene]
- decaprenyl pyrophosphate synthetase [MeSH Supplementary Concept]
- ischiocoxopodopatellar syndrome [DO Concept]
- sonic hedgehog signaling molecule [ORDO Gene]
- spermine synthase [ORDO Gene]
- sucrose-phosphate synthase activity [GO term]
- triose-phosphate:phosphate antiporter activity [GO term]
- ubiquinone Q1 [MeSH Supplementary Concept]
HGNC gene
- decaprenyl diphosphate synthase subunit 1 [HGNC gene]
ORDO concept(s)
- decaprenyl diphosphate synthase subunit 1 [ORDO Gene]
Phenotypes related
- Coenzyme q10 deficiency, primary, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- decaprenyl diphosphate synthase subunit 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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