B4GT6 Polyclonal Antibody, 20ul Plates & Dishes Mutations in this gene have

Mutations in this gene have been associated with the Proteus syndrome

Loss of expression of the related gene in mouse affects coat and eye pigmentation

CBFA2T3 (CBFA2/RUNX1 translocation partner 3) encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression

5-trisphosphate 3-kinase is responsible for regulating the levels of a large number of inositol polyphosphates that are important in cellular signaling

Mutations causing Bloom syndrome delete or alter helicase motifs and may disable the 3'-5' helicase activity

B4GT6 Polyclonal Antibody, 20ul Plates & Dishes Mutations in this gene haveThis gene is one of seven beta 1,4 galactosyltransferase (beta4GalT) genes. They encode type II membrane bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have