Mitochondrial inner membrane protein of unknown function; associates with mitochondrial ribosome; localizes to the inner membrane with the C terminus facing the intermembrane space; ortholog of human RMND1, mutation in which is implicated in infantile encephaloneuromyopathy and defective mitochondrial translation [Source:SGD;Acc:S000002690]

Chromosome IV: 1,023,511-1,024,755 reverse strand.

R64-1-1:BK006938.2

This gene has 1 transcript (splice variant), 222 orthologues, 2 paralogues and is a member of 1 Ensembl protein family.

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