GSHB Polyclonal Antibody, 50ul sgRNA Oligos Mutations in this gene cause

Mutations in this gene cause Omenn syndrome

Matrix metallopeptidase 17 is unique among the membrane-type matrix metalloproteinases in that it is anchored to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor

BCL2L2 encodes a member (BCL2 like 2)of the BCL-2 protein family

|PTM:Ubiquitinated

Vasodilator-stimulated phosphoprotein (VASP) is a member of the Ena-VASP protein family

GSHB Polyclonal Antibody, 50ul sgRNA Oligos Mutations in this gene causeGlutathione is important for a variety of biological functions, including protection of cells from oxidative damage by free radicals, detoxification of xenobiotics, and membrane transport. The protein encoded by this gene functions as a homodimer to catalyze the second step of glutathione biosynthesis, which is the ATP dependent conversion of gamma L glutamyl L cysteine to glutathione. Defects in this gene are a cause of glutathione synthetase