Your search for "ift43" returned 259 TaqMan® SNP Genotyping Assays
intraflagellar transport 43
This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
1700019E19RIK, C14ORF179, CED3, IFT43, R75064, RGD1307392
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