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

Mutations of this gene are associated with progressive pseudorheumatoid dysplasia

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

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

Binds to a large number of partners

Osteoglycin Polyclonal Antibody, 50ul Shaker&Mixing Mutations of 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.