 | Decaprenyl-diphosphate synthase subunit 1 is an enzyme that in humans is encoded by the PDSS1 gene. The protein encoded by this gene is an enzyme that elongates the prenyl... 6 KB (594 words) - 11:40, 17 October 2022 |
 | does not reduce side effects of statin medications. Genes involved include PDSS1, PDSS2, COQ2, and ADCK3 (COQ8, CABC1). Organisms other than humans produce... 48 KB (4,859 words) - 15:37, 23 April 2024 |
 | primary; ubiquinone deficiency; Coenzyme Q deficiency; CoQ deficiency) COQ2, PDSS1, PDSS2, ADCK3, COQ9, COQ4, COQ7, COQ5 AR PS607426 Mitochondrial complex... 40 KB (3,236 words) - 06:39, 15 April 2024 |
Q9NUG6 11918 PDS5A HGNC:29088 Q29RF7 11919 PDS5B HGNC:20418 Q9NTI5 11920 PDSS1 HGNC:17759 Q5T2R2 11921 PDSS2 HGNC:23041 Q86YH6 11922 PDX1 HGNC:6107 P52945... 282 KB (17 words) - 22:06, 12 April 2024 |
 | deficiency of coenzyme Q10. It can be associated with COQ2, APTX, PDSS2, PDSS1, CABC1, and COQ9. Some forms may be more treatable than other mitochondrial... 2 KB (101 words) - 11:05, 22 October 2022 |
 | I, Schlemmer D, et al. (2007). "Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency... 5 KB (632 words) - 00:50, 3 December 2023 |
Coenzyme Q10 deficiency; 607426; COQ9 Coenzyme Q10 deficiency; 607426; PDSS1 Coenzyme Q10 deficiency; 607426; PDSS2 Coffin–Lowry syndrome; 303600; RPS6KA3... 234 KB (18,877 words) - 12:36, 2 April 2024 |
 | coenzyme Q biosynthesis. It may be associated with Coenzyme Q10 deficiency. PDSS1 GRCh38: Ensembl release 89: ENSG00000164494 – Ensembl, May 2017 GRCm38:... 6 KB (732 words) - 23:29, 3 March 2023 |