TGFB1 and coronary artery disorder: Li et al. [47] identified 61 CHD recessive genes from a global mouse mutagenesis screen and consistently found half of them to be involved in cilia-related structures or pathways, such as IFT transport, cilia assembly, ciliary pocket, basal body, outer dynein arm, inversin compartment and transition zone, SHH signaling, WNT/planar cell polarity signaling, TGF-β/BMP signaling, and calcium signaling [47].