Survivin Monoclonal Antibody, 100ul Custom Peptide Synthesis disease:Defects in OSMR are the

disease:Defects in OSMR are the cause of amyloidosis type 9 (AMYL9)

which differ only at the 5' end

This gene encodes a coiled-coil protein that plays a role in multiple processes including cytoskeletal organization

the full-length sequence of some variants has not been determined

which may include one of several different cyclins along with cyclin-dependent kinase 9

Survivin Monoclonal Antibody, 100ul Custom Peptide Synthesis disease:Defects in OSMR are theThis gene is a member of the inhibitor of apoptosis (IAP) gene family, which encode negative regulatory proteins that prevent apoptotic cell death. IAP family members usually contain multiple baculovirus IAP repeat (BIR) domains, but this gene encodes proteins with only a single BIR domain. The encoded proteins also lack a C terminus RING finger domain. Gene expression is high during fetal development and in most tumors, yet low in adult tissues.