TIMM17A (Translocase Of Inner Mitochondrial Membrane 17A) is a Protein Coding gene. Diseases associated with TIMM17A include Barth Syndrome and Mohr-Tranebjaerg Syndrome. Among its related pathways are Metabolism of proteins and Mitochondrial protein import. Gene Ontology (GO) annotations related to this gene include P-P-bond-hydrolysis-driven protein transmembrane transporter activity. An important paralog of this gene is TIMM17B.