Gene Review:
MTO1 - mitochondrial tRNA translation optimization 1
Homo sapiens
Synonyms:
CGI-02, COXPD10, Protein MTO1 homolog, mitochondrial
- Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation. Li, X., Li, R., Lin, X., Guan, M.X. J. Biol. Chem. (2002)
- Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3. Bykhovskaya, Y., Mengesha, E., Wang, D., Yang, H., Estivill, X., Shohat, M., Fischel-Ghodsian, N. Mol. Genet. Metab. (2004)