FOG16283
EOG88SF9M

sce:MRX10

Genes: 29

SGD Description
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


AspGD Description
Ortholog(s) have role in cellular response to biotic stimulus, cellular response to starvation and filamentous growth of a population of unicellular organisms in response to biotic stimulus, more


References

Garcia-Diaz B, et al. (2012 Oct 5). Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation.

Kehrein K, et al. (2015 Feb 12). Organization of Mitochondrial Gene Expression in Two Distinct Ribosome-Containing Assemblies.

Mitochondrial localization predictions
Predotar	TargetP	MitoProt
Raw data
Phobius transmembrane predictions 29 genes with posterior transmembrane prediction > 50%