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IFT88

Intraflagellar transport protein 88 homolog is a protein that is encoded by the IFT88 gene.

Function
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. == Interactions ==
Interactions
IFT88 has been shown to interact with BAT2 and WDR62. WDR62 is required for IFT88 localization to the cilia basal body and the cilia axoneme. == References ==
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