CD238 Polyclonal Antibody, 100ul Polyclonal Antibodies Mutations in this gene have

Mutations in this gene have been associated with thrombophilia due to protein C deficiency| neonatal purpura fulminans| and recurrent venous thrombosis

FZD7 expression may downregulate APC function and enhance beta-catenin-mediated signals in poorly differentiated human esophageal carcinomas

sometimes including retinal dystrophy and renal disease

which is the major protein component of high density lipoprotein (HDL) in plasma

delta and epsilon

CD238 Polyclonal Antibody, 100ul Polyclonal Antibodies Mutations in this gene haveKEL (Kell blood group, metallo endopeptidase) encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen. The Kell glycoprotein links via a single disulfide bond to the XK membrane protein that carries the Kx antigen. The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases.