3-oxoacid CoA-transferase 1 (OXCT1) is an enzyme that in humans is encoded by the OXCT1 gene. It is also known as succinyl-CoA-3-oxaloacid CoA transferase...
11 KB (1,423 words) - 20:21, 6 October 2023
field of Science and Technology Studies SCOT, an enzyme encoded by the OXCT1 gene S.C.O.T., a rap album Scot (given name) Scot (surname) All pages with...
788 bytes (150 words) - 21:29, 15 August 2022
only one. The CoA-transferases have been divided into six families (Cat1, OXCT1, Gct, MdcA, Frc, CitF) based on their amino acid sequences and reactions...
10 KB (1,316 words) - 01:10, 4 September 2024
beta-oxidation, in the genes for ketogenesis (HMGCS2 and HMGCL), for ketolysis (OXCT1, ACAT1). Defects in this pathway can cause varying degrees of inability...
19 KB (2,337 words) - 16:33, 17 August 2024
Q9BRP0 11577 OVOL3 HGNC:14186 O00110 11578 OXA1L HGNC:8526 Q15070 11579 OXCT1 HGNC:8527 P55809 11580 OXCT2 HGNC:18606 Q9BYC2 11581 OXER1 HGNC:24884 Q8TDS5...
282 KB (17 words) - 08:00, 19 November 2024
succinyl-coenzyme A to acetoacetate. It can be caused by mutation in the OXCT1 gene. First described in 1972,there are 34 known people to have been reported...
2 KB (183 words) - 16:06, 25 April 2023
lead to coma and death. The deficiency is caused by mutation in the gene OXCT1. Treatments mostly rely on controlling the diet of the patient. Carnitine...
60 KB (6,229 words) - 00:37, 7 October 2024
271980; ALDH5A1 Succinyl-CoA:3-oxoacid CoA transferase deficiency; 245050; OXCT1 Sucrase-isomaltase deficiency, congenital; 222900; SI Sudden infant death...
234 KB (18,877 words) - 06:16, 6 November 2024