“…In mice, ENPP1 is expressed in plasma cells, on hepatocytes, renal tubules, salivary duct epithelium, epididymis, capillary endothelium in the brain, and chondrocytes (Harahap and Goding 1988). In man it has been shown that ENPP1 is expressed in liver, cartilage and bone, and is thought to regulate physiological mineralization processes and pathological chondrocalcinosis (Huang, Rosenbach et al 1994). Homozygous mutations in ENPP1 are known to cause generalized arterial calcifications of infancy (GACI) (Rutsch, Vaingankar et al 2001;Rutsch, Ruf et al 2003).…”