Your search for "cc2d2a" returned 337 TaqMan® SNP Genotyping Assays
coiled-coil and C2 domain containing 2A
This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
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