Automated description from the Alliance of Genome Resources
Predicted to contribute to NADH dehydrogenase activity. Predicted to be involved in mitochondrial ATP synthesis coupled electron transport and response to oxidative stress. Localizes to the mitochondrion. Human ortholog(s) of this gene implicated in Leigh disease; hypertrophic cardiomyopathy; inherited metabolic disorder; mitochondrial complex I deficiency; and multiple sclerosis. Orthologous to human NDUFS2 (NADH:ubiquinone oxidoreductase core subunit S2).