CHRFAM7A and lung disorder: 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).