Osteoglycin Polyclonal Antibody, 50ul Shaker&Mixing Mutations in this gene are

Mutations in this gene are associated with the congenital disorder of glycosylation type IIe

Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy

which are typical of the ADAMTS family

DQX1 is encoded by a gene that maps to human chomosome 2

These carbonic anhydrases are a class of metalloenzymes that catalyze the reversible hydration of carbon dioxide and are differentially expressed in a number of cell types

Osteoglycin Polyclonal Antibody, 50ul Shaker&Mixing Mutations in this gene areOGN encodes a member of the small leucine rich proteoglycan (SLRP) family of proteins. The osteoglycin induces ectopic bone formation in conjunction with transforming growth factor beta and may regulate osteoblast differentiation. High expression of the encoded protein may be associated with elevated heart left ventricular mass. Alternative splicing results in multiple transcript variants.