WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in this gene result

Mutations in this gene result in one form of autosomal dominant hearing impairment

Binding to he LCK SH3 domain occurs constitutively

The encoded protein is widely distributed among animals and cleaves DNA at GC tracts

These mRNAs arise from the long MBP gene (otherwise called "Golli-MBP") that contains 3 additional exons located upstream of the classic MBP exons

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in this gene resultThis gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly his and trp asp (GH WD) which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression signal transduction apoptosis and gene regulation. This gene is highly expressed in