BOP1 Polyclonal Antibody, 100ul sgRNA Oligos an autosomal dominant disorder characterized

an autosomal dominant disorder characterized by numerous small white flecks present in all layers of the corneal stroma

The encoded protein is a member of the FAK subfamily of protein tyrosine kinases but lacks significant sequence similarity to kinases from other subfamilies

This gene is located adjacent to a related alpha subunit gene

and changes in glycosylation of this protein have been associated with carcinomas

|subunit:Interacts with ZBTB7 and BCL6B (By similarity)

BOP1 Polyclonal Antibody, 100ul sgRNA Oligos an autosomal dominant disorder characterizedComponent of the PeBoW complex, which is required for maturation of 28S and 5. 8S ribosomal RNAs and formation of the 60S ribosome.,induction: By MYC.,Belongs to the WD repeat BOP1 ERB1 family.,Contains 7 WD repeats.,subunit: Component of the PeBoW complex, composed of bop1, pes1 and wdr12. Within the PeBoW complex bop1 interacts directly with pes1 and wdr12. The PeBoW complex also associates with the 66S pre ribosome.,