CD63 Polyclonal Antibody, 100ul[BT-AP01939] Cell Labeling & Imaging Mutations in this gene have

Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

subunit:Binds to actin

This gene encodes a seven-transmembrane protein that belongs to the family 1 of G-protein coupled receptors

This gene lies in close proximity to

This gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins and sequestering them in latent complexes

CD63 Polyclonal Antibody, 100ul[BT-AP01939] Cell Labeling & Imaging Mutations in this gene haveKallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. KLK8 is one of the fifteen kallikrein subfamily members located in tandem in a gene cluster on chromosome 19. Kallikrein related peptidase 8 may be involved in proteolytic cascade in the skin and may serve as a