The ATP-binding cassette 6 transporter (ABCC6), one of the ABCC subfamily members, is mainly known because gene mutations are responsible for pseudoxanthoma elasticum (PXE), a rare autosomal recessive disease characterized by a progressive ectopic calcification of elastic fibers in dermal, ocular, and vascular tissues [1,2,3]. The gene discussed is ABCA3; the disease is Pseudoxanthoma elasticum.