Your search for "ift80" returned 255 TaqMan® SNP Genotyping Assays
intraflagellar transport 80
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]
4921524P20RIK, ATD2, IFT80, MKIAA1374, RGD1312006, SRTD2, WDR56
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