Protein 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 encoding multiple isoforms have been observed for this gene.

Gene names and symbols associated with ACSF3

• acyl-CoA synthetase family member 3 (ACSF3) antibody
• acyl-CoA synthetase family member 3 (Acsf3) antibody

• BB101783 antibody

Protein level used designations for ACSF3

acyl-CoA synthetase family member 3, mitochondrial , malonyl-CoA synthetase