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IFT80

Official Full Name
intraflagellar transport 80
Organism
Homo sapiens
GeneID
57560
Background
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.[provided by RefSeq, Jun 2010]
Synonyms
ATD2; SRTD2; WDR56; FAP167; CFAP167;

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