From 3′→5′, they are ERCC2/XPD (excision repair cross-complementing rodent repair deficiency, complementation group 2/xeroderma pigmentosum complementary group D), PPP1R13L/IASPP/RAI [protein phosphatase 1, regulatory (inhibitor) subunit 13 like/Inhibitory member of the ASPP family/RelA-associated inhibitor], CD3EAP/ASE-1 [CD3e molecule, epsilon-associated protein/antisense to ERCC1)], and ERCC1 (excision repair cross-complementing rodent repair deficiency, complementation group 1) (Figure 1). The gene discussed is PPP1R13L; the disease is xeroderma pigmentosum.