Automated description from the Alliance of Genome Resources
Predicted to have lipid binding activity and protein homodimerization activity. Involved in mitochondrial electron transport, NADH to ubiquinone and ubiquinone biosynthetic process. Localizes to the mitochondrion. Used to study coenzyme Q10 deficiency disease. Human ortholog(s) of this gene implicated in primary coenzyme Q10 deficiency 5. Orthologous to human COQ9 (coenzyme Q9).