The genes FOXP1, PAPPA, FLRT2, LMO7, DPYSL3, RAI14, SIK3, DAAM2, MYOM1, SLIT1, MOAP1, MAML3, NES, CBX4, and METTL3 had mutations in indolent PCa only (Table 1). The gene discussed is SIK3; the disease is posterior cortical atrophy.