CD168 Polyclonal Antibody, 100ul[BT-AP01380] Miscellaneous Type II hyperoxaluria is caused

Type II hyperoxaluria is caused by mutations in this gene

and cleft lip/palate syndrome 3 (EEC3)

Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to TGF-beta signaling

This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly

It is also found in abundance in the germ cells of testis and ovary

CD168 Polyclonal Antibody, 100ul[BT-AP01380] Miscellaneous Type II hyperoxaluria is causedThe hyaluronan mediated motility receptor encoded by HMMR is involved in cell motility. It is expressed in breast tissue and together with other proteins, it forms a complex with BRCA1 and BRCA2, thus is potentially associated with higher risk of breast cancer. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.