TIMM17A (translocase of inner mitochondrial membrane 17 homolog A (yeast)) is a protein-coding gene. Diseases associated with TIMM17A include barth syndrome, and breast cancer, and among its related super-pathways are Post-translational protein modification. GO annotations related to this gene include P-P-bond-hydrolysis-driven protein transmembrane transporter activity. An important paralog of this gene is TIMM17B. Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane.
Pathway
Metabolism of proteins; Mitochondrial Protein Import;
Citations
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