Cytochrome P450 4V2 is a protein that in humans is encoded by the CYP4V2 gene. Mutations are associated with Bietti's crystalline dystrophy and retinitis...
6 KB (662 words) - 04:52, 15 December 2023
Q9HBI6 3903 CYP4F12 HGNC:18857 Q9HCS2 3904 CYP4F22 HGNC:26820 Q6NT55 3905 CYP4V2 HGNC:23198 Q6ZWL3 3906 CYP4X1 HGNC:20244 Q8N118 3907 CYP4Z1 HGNC:20583 Q86W10...
277 KB (17 words) - 23:17, 27 April 2024
signs or symptoms of the disorder. BCD is associated with mutations in the CYP4V2 gene. The nematode C. elegans has a duplicated gene (cyp31A2 and cyp31A3)...
5 KB (476 words) - 06:31, 26 July 2023
CYP4A11, CYP4A22, CYP4B1, CYP4F2, CYP4F3, CYP4F8, CYP4F11, CYP4F12, CYP4F22, CYP4V2, CYP4X1, CYP4Z1 Too many to list CYP5 thromboxane A2 synthase 1 subfamily...
42 KB (4,485 words) - 22:27, 17 July 2024
myopathy; 158810; COL6A3 Bietti crystalline corneoretinal dystrophy; 210370; CYP4V2 Bifid nose with or without anorectal and renal anomalies; 608980; FREM1...
234 KB (18,877 words) - 15:43, 9 May 2024
that are 10-16 carbons long; CYP4A11, CYP4F2, CYP4F3A, CYP4F3B, CYP4F11, CYP4V2, and CYP4Z1 also metabolize these fatty acids. Subsequent to their ω-hydroxylation...
14 KB (1,685 words) - 02:13, 17 June 2024
Other genes are also found nearby on the same chromosome, including TLR3, CYP4V2, FLJ38576, ORAOV1P1, and SORBS2. FAM149A possess one major paralog, FAM149B...
18 KB (1,841 words) - 09:07, 10 March 2024