Cripto-3 Polyclonal Antibody, 50ul Cytokines Defects in this gene are

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

Several alternatively spliced transcript variants of CEP170 have been found

They are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport

this protein forms a complex with STAT1 and IFN regulatory factor family protein p48 (ISGF3G)

It is also responsible for inducing catalase activity and therefore enhancing cell motility

Cripto-3 Polyclonal Antibody, 50ul Cytokines Defects in this gene areThe TDGF3 locus has characteristics of a retrotransposon, including lack of introns and a poly(A) sequence.