by the COQ2 gene. CoQ (ubiquinone) serves as a redox carrier in the mitochondrial respiratory chain and is a lipid-soluble antioxidant. COQ2, or...
5 KB (632 words) - 00:50, 3 December 2023
side effects of statin medications. Genes involved include PDSS1, PDSS2, COQ2, and ADCK3 (COQ8, CABC1). Organisms other than humans produce the benzoquinone...
49 KB (4,946 words) - 17:51, 3 August 2024
HGNC:21314 Q8WXC6 3427 COPZ1 HGNC:2243 P61923 3428 COPZ2 HGNC:19356 Q9P299 3429 COQ2 HGNC:25223 Q96H96 3430 COQ3 HGNC:18175 Q9NZJ6 3431 COQ4 HGNC:19693 Q9Y3A0...
277 KB (17 words) - 23:17, 27 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) - 17:28, 19 September 2024
Q10 deficiency is a deficiency of coenzyme Q10. It can be associated with COQ2, APTX, PDSS2, PDSS1, CABC1, and COQ9. Some forms may be more treatable than...
2 KB (101 words) - 11:05, 22 October 2022
"Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders"...
6 KB (594 words) - 11:40, 17 October 2022
PMID 14574404. Diomedi-Camassei F, Di Giandomenico S, Santorelli FM, et al. (2007). "COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal...
6 KB (732 words) - 23:29, 3 March 2023
Coenzyme Q10 deficiency; 607426; CABC1 Coenzyme Q10 deficiency; 607426; COQ2 Coenzyme Q10 deficiency; 607426; COQ9 Coenzyme Q10 deficiency; 607426; PDSS1...
234 KB (18,877 words) - 15:43, 9 May 2024