The remaining 11 genes in the region encode proteins associated with neurologic disorders (APBA2, CHRFAM7A, MTMR10, FAN1), skin and eye pigmentation or development (OCA2, HERC2, TJP1, TRPM1), nephritis (ARHGAP11B, MTMR10, FAN1), and lung disease (ENTREP2, NSMCE3). The gene discussed is ARHGAP11B; the disease is lung disorder.