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

PTM:It is not sure whether N-glycosylation is on Asn-165 and/or Asn-166

Defects in this gene are associated with the disorder common variable immunodeficiency-8 with autoimmunity

Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor

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

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.