PGLS Polyclonal Antibody, 100ul Modification Enzymes Defects in F12 do not

Defects in F12 do not cause any clinical symptoms and the sole effect is that whole-blood clotting time is prolonged

which regulates its rapid exchange between the plasma membrane and the Golgi apparatus

The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins

and the NF-kB precursor p105 in vitro

The protein encoded by this gene belongs to the tensin family

PGLS Polyclonal Antibody, 100ul Modification Enzymes Defects in F12 do notPGLS (6 Phosphogluconolactonase) is a Protein Coding gene. Diseases associated with PGLS include lymphatic system disease. Among its related pathways are Metabolism and Glycosaminoglycan metabolism. Gene Ontology (GO) annotations related to PGRMC2 include monosaccharide binding and 6 phosphogluconolactonase activity.