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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