IFT80 Back

intraflagellar transport 80 homolog (Chlamydomonas)

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NCBI Description of IFT80

The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.

Community Annotation of IFT80 Add / Edit IFT80: Annotations

No community annotations yet for IFT80.
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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).


IFT80 is highly significantly mutated in
IFT80 is significantly mutated in
IFT80 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for IFT80