EC Number | Application | Comment | Organism |
---|---|---|---|
1.3.8.1 | medicine | short-chain-acyl-CoA-dehydrogenase deficiency is an inborn error of mitochondrial fatty acid metabolism caused by rare mutations as well as common susceptibility variations in the SCAD gene | Homo sapiens |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.3.8.1 | Homo sapiens | - |
- |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.3.8.1 | butyryl-CoA + electron acceptor | - |
Homo sapiens | 2-butenoyl-CoA + reduced acceptor | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.3.8.1 | SCAD | - |
Homo sapiens |
1.3.8.1 | short-chain acyl-CoA dehydrogenase | - |
Homo sapiens |