CD105 Monoclonal Antibody, 100ul Multi-Layer Cell Culture System This gene is found within

This gene is found within an intron of another gene| bladder cancer associated protein| but on the opposite strand

Mutations in this gene cause nephronophthisis (NPHP)| an autosomal recessive kidney disease characterized by tubular basement membrane disruption| interstitial lymphohistiocytic cell infiltration| and development of cysts at the corticomedullary border of the kidneys

lymphocyte recirculation

May be involved in regulation of apoptosis

CD105 Monoclonal Antibody, 100ul Multi-Layer Cell Culture System This gene is found withinThis gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler Rendu Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be