CD55 Polyclonal Antibody, 100ul[BT-AP02187] Miscellaneous and heterozygous deletion of the

and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype

CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD)

Binds phospholipid vesicles containing phosphatidylinositol 3-phosphate and participates in endosomal trafficking

This gene has also been identified as a co-activator of HIF1A (hypoxia-inducible factor 1 alpha)

CD55 Polyclonal Antibody, 100ul[BT-AP02187] Miscellaneous and heterozygous deletion of thePLA2G4E (Phospholipase A2 Group IVE) is a Protein Coding gene. Among its related pathways are Metabolism and Glycerophospholipid biosynthesis. GO annotations related to this gene include phospholipase A2 activity and phospholipase activity. An important paralog of this gene is JMJD7 PLA2G4B. alcium dependent phospholipase A2 that selectively hydrolyzes glycerophospholipids in the sn 2 position. hospholipases are a group of enzymes that hydrolyze