The genes EPHB1, KIAA1614, SACS, SMAD4, PCDHA1, TNS1, CACNA1C, DEPDC1, PCDHGA9, LRP4, KLHL2, CDC20, ARHGEF39, CGNL1, SKIV2L2, FAM196A, IL6ST, ATP2B4, TGFBR3, TIGD3, NOS1, SRSF2, MYO9A, KIF13A, UBR3, WIF1, LRGUK, ERBB4, and NYNRIN had mutations in aggressive PCa only (Table 1). The gene discussed is INSYN2A; the disease is posterior cortical atrophy.