DVL1 and coronary artery disorder: Genes that may contribute to the development of CHD and CMP associated with 1p36 deletions are DVL1, SKI, RERE, PDPN, SPEN, CLCNKA, ECE1, HSPG2, LUZP1, WASPF2, SKI, PRKCZ, PRDM16, RERE, UBE4B, and MASP2.