Automated description from the Alliance of Genome Resources
Predicted to have 3-hydroxyacyl-CoA dehydrogenase activity and enzyme binding activity. Involved in fatty acid beta-oxidation. Localizes to the mitochondrion. Human ortholog(s) of this gene implicated in Fanconi syndrome. Is expressed in several structures, including alimentary system; liver; nervous system; respiratory system; and sensory organ. Orthologous to human EHHADH (enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase).