During development, CXCL12 drives migration of cells expressing CXCR4, including ECs (Li et al., 2013) and neural crest (Belmadani et al., 2005; Escot et al., 2013; Theveneau et al., 2010), while knockout studies have shown that mice lacking either CXCL12 or CXCR4 die in utero or perinatally, with identical defects in hematopoiesis and cerebellar development as well as a cardiac ventricular septal defect (VSD) (Nagasawa et al., 1996, Ma et al., 1998, Tachibana et al., 1998, Zou et al., 1998). This evidence concerns the gene CXCR4 and ventricular septal defect.