TUFM Back

Tu translation elongation factor, mitochondrial

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NCBI Description of TUFM
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.

Community Annotation of TUFM Add / Edit TUFM: Annotations

No community annotations yet for TUFM.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

TUFM is highly significantly mutated in
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TUFM is significantly mutated in
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TUFM is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for TUFM