Frizzled-6 Polyclonal Antibody, 100ul[BT-AP03366] Syringe Filter Defects in this gene are

Defects in this gene are a cause of macular corneal dystrophy (MCD)

a disease characterized by muscular rigidity

Catalyzes the cross-linking of proteins and the conjugation of polyamines to specific proteins in the seminal tract

Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of this gene have been identified

Frizzled-6 Polyclonal Antibody, 100ul[BT-AP03366] Syringe Filter Defects in this gene areFZD6 (frizzled class receptor 6) represents a member of the frizzled gene family, which encode 7 transmembrane domain proteins that are receptors for Wnt signaling proteins. The protein encoded by this family member contains a signal peptide, a cysteine rich domain in the N terminal extracellular region, and seven transmembrane domains, but unlike other family members, this protein does not contain a C terminal PDZ domain binding motif. This protein