IFT88 Back

intraflagellar transport 88 homolog (Chlamydomonas)

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NCBI Description of IFT88

This gene encodes a member of the tetratrico peptide repeat (TPR) family. Mutations of a similar gene in mouse can cause polycystic kidney disease. Two transcript variants encoding distinct isoforms have been identified for this gene.

Community Annotation of IFT88 Add / Edit IFT88: Annotations

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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

IFT88 is highly significantly mutated in
(none)
IFT88 is significantly mutated in
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IFT88 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 IFT88