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Using data from mouse models where evidence for genetic variation in susceptibility to APAP DILI has also been obtained, polymorphisms in a set of candidate genes were genotyped in approximately 120 individuals for whom data on circulating ALT following APAP administration at 4 g per day for 7 days was available.67 Polymorphisms in CD44 (rs1467558), which codes for a protein involved in lymphocyte adhesion and activation, and in CAPN10 (rs3749166) which encodes a protease released following hepatocyte damage, were predictive for the extent of ALT elevation with borderline significant effects seen for those carrying rs1467558 or rs3749166