PROM1 and cone-rod dystrophy: Indeed, in the hCOR list (excluding shared genes), 7 genes (AHI1, ATXN7, KCNV2, PROM1, RD3, RPGRIP1) have been linked to human CRD or Leber’s congenital amaurosis (LCA) diseases, while mCOR list only contains one such gene (GUCA1A).