Automated description from the Alliance of Genome Resources (Release 7.0.0)
Predicted to be involved in positive regulation of mitochondrial translation. Predicted to act upstream of or within translation. Located in mitochondrion. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 11. Orthologous to human RMND1 (required for meiotic nuclear division 1 homolog).