CBY1 Rabbit Polyclonal Antibody, 50ul Recombinant Protein It is also a candidate

It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome

Mutations in this gene result in autosomal dominant Char syndrome

This represents the last step in the phototransduction pathway

Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lact

CBY1 Rabbit Polyclonal Antibody, 50ul Recombinant Protein It is also a candidateBeta catenin is a transcriptional activator and oncoprotein involved in the development of several cancers. The protein encoded by this gene interacts directly with the C terminal region of beta catenin, inhibiting oncogenic beta catenin mediated transcriptional activation by competing with transcription factors for binding to beta catenin. Two transcript variants encoding different isoforms have been found for this gene.