FOXP1 and posterior cortical atrophy: 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).