TIMM8A
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Mitochondrial import inner membrane translocase subunit Tim8 A is an enzyme that in humans is encoded by the TIMM8A gene.[1][2][3]
This translocase has similarity to yeast mitochondrial proteins that are involved in the import of metabolite transporters from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Deafness-dystonia syndrome (or Mohr-Tranebjaerg syndrome; MTS/DFN-1) and it is postulated that MTS/DFN-1 is a mitochondrial disease caused by a defective mitochondrial protein import system.[3]
Alternative names
- Deafness-dystonia peptide
- Deafness-dystonia protein
Interactions
TIMM8A has been shown to interact with Signal transducing adaptor molecule[4] and TIMM13.[5][6]
References
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External links
- The Deafness Dystonia Protein DDP and Mitochondrial Division - a free videolecture by Craig Blackstone, 2002.
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