TBL2 Polyclonal Antibody, 100ul sgRNA Oligos Mutations in this gene have

Mutations in this gene have been reported to be associated with nonsyndromic hearing loss

Some of its substrates include proparathyroid hormone

It contains a set of putative metal binding motifs with similarity to that seen in a family of membrane desaturases-hydroxylases

36) family

TBL2 Polyclonal Antibody, 100ul sgRNA Oligos Mutations in this gene haveTBL2 encodes a member of the beta transducin protein family. Most proteins of the beta transducin family are involved in regulatory functions. transducin beta like 2 is possibly involved in some intracellular signaling pathway. TBL2 is deleted in Williams Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11. 3.