known as IMP dehydrogenase 2, is an enzyme that in humans is encoded by the IMPDH2 gene. IMP dehydrogenase 2 is the rate-limiting enzyme in the de novo guanine...
9 KB (1,112 words) - 06:54, 22 April 2024
two distinct isozymes of IMPDH encoded by two distinct genes, IMPDH1 and IMPDH2. Both isozymes contain 514 residues, have an 84% similarity in peptide sequence...
24 KB (2,554 words) - 03:58, 26 May 2025
CC2D2A, OFD1, TMEM138, TCTN3, ZNF423, AMRC9 Juvenile-onset dystonia ACTB, IMPDH2 dominant Juvenile primary lateral sclerosis (JPLS) ALS2 Keloid disorder...
43 KB (995 words) - 23:45, 24 May 2025
ion transporters such as CorA. lectins such as Concanavalin A IMPDH and IMPDH2 Examples of heterotetramers include haemoglobin (pictured), the NMDA receptor...
11 KB (1,224 words) - 05:47, 26 March 2025
of juvenile-onset dystonia. Another gene associated with the disorder is IMPDH2. "Dystonia, juvenile-onset". www.uniprot.org. Retrieved 2022-05-15. "Search...
6 KB (509 words) - 16:41, 30 March 2025
O14732 7650 IMPACT HGNC:20387 Q9P2X3 7651 IMPDH1 HGNC:6052 P20839 7652 IMPDH2 HGNC:6053 P12268 7653 IMPG1 HGNC:6055 Q17R60 7654 IMPG2 HGNC:18362 Q9BZV3...
277 KB (17 words) - 18:41, 6 October 2024
Sasaki T, et al. (2009). "Genetic variations in the HGPRT, ITPA, IMPDH1, IMPDH2, and GMPS genes in Japanese individuals". Drug Metab. Pharmacokinet. 24...
9 KB (1,110 words) - 14:50, 23 February 2024