In their paper, Vishnolia et al. exploited the possibilities of this model to highlight that two genes, CNNM2 and NT5C2, identified by GWAS at the human 10q24.32 locus, among other putative genes (CYP17A1, BORCS7, AS3MT, CNNM2, and NT5C2), predispose to hypertension (25). Here, CYP17A1 is linked to hypertensive disorder.