Your search for "ift172" returned 219 TaqMan® SNP Genotyping Assays
intraflagellar transport 172
This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]
4930553F24RIK, AVC1, BBS20, IFT172, NPHP17, OSM-1, RP71, SLB, SRTD10, WIM
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