Automated description from the Alliance of Genome Resources (Release 7.5.0)
Predicted to enable identical protein binding activity and tRNA binding activity. Predicted to be involved in RNA processing and positive regulation of mitochondrial translation. Located in mitochondrion. Is expressed in several structures, including central nervous system; metanephros; phalanx; skin; and tooth. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 30. Orthologous to human TRMT10C (tRNA methyltransferase 10C, mitochondrial RNase P subunit).
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