| Gene Symbol | ACSF3 |
| Entrez Gene ID | 197322 |
| Full Name | acyl-CoA synthetase family member 3 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]. |
| Disorder MIM: | |
| Disorder Html: | Combined malonic and methylmalonic aciduria, 614265 (3) |









































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