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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACSF3-20-RE | 20 (40 μL) | 200 μL |  |
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| ACSF3-20-OR | 20 (40 μL) | 200 μL |  |
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| ACSF3-20-GO | 20 (40 μL) | 200 μL |  |
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| ACSF3-20-GR | 20 (40 μL) | 200 μL |  |
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| ACSF3-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : ACSF3
Gene Name : Acyl-CoA synthetase family member 3
Chromosome : CHR 16: 890,938,08-891,605,55
Locus : 16q24.3
Alt. Genes : ZNF263
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