Samiksha Jaiswal (Editor)

TIMM8A

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Species
  
Human

Entrez
  
1678

Human
  
Mouse

Ensembl
  
ENSG00000126953

TIMM8A

Aliases
  
TIMM8A, DDP, DDP1, DFN1, MTS, TIM8, translocase of inner mitochondrial membrane 8 homolog A (yeast)

External IDs
  
MGI: 1353433 HomoloGene: 37878 GeneCards: TIMM8A

Mitochondrial import inner membrane translocase subunit Tim8 A is an enzyme that in humans is encoded by the TIMM8A gene.

Contents

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.

Alternative names

  • Deafness-dystonia peptide
  • Deafness-dystonia protein
  • Interactions

    TIMM8A has been shown to interact with Signal transducing adaptor molecule and TIMM13.

    References

    TIMM8A Wikipedia