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Table 1 The 156 retinal diseases-related genes enrolled in our targeted region sequencing

From: Identification of a novel RHO heterozygous nonsense mutation in a Chinese family with autosomal dominant retinitis pigmentosa

ABCA4, ABHD12, ADAM9, ADGRV1, AIPL1, ALMS1, ARL2BP, ARL6, BBS1, BBS2, BEST1, BMP4, C2orf71, C8orf37, CA4, CABP4, CACNA1F, CACNA2D4, CAPN5, CDH23, CEP290, CERKL, CHM, CIB2, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CNNM4, COL2A1, COL4A1, COL9A1, CRB1, CRX, CYP4V2, DHDDS, EFEMP1, ELOVL4, EMC1, ERBB3, EYS, FAM161A, FLVCR1, FSCN2, FZD4, GDF6, GNAT1, GNAT2, GPR179, GRK1, GRM6, GRN, GUCA1A, GUCA1B, GUCY2D, HARS, HGSNAT, HK1, IDH3B, IFT140, IFT172, IMPDH1, IMPG2, INPCDHR1, IQCB1, ITM2B, KCNJ13, KCNV2, KIF11, KLHL7, LCA5, LRAT, LRIT3, LRP5, MAK, MERTK, MFSD8, MVK, MYO7A, NDP, NEK2, NMNAT1, NR2E3, NRL, NYX, OFD1, OTX2, P3H2, P5E, PCDH15, PCYT1A, PDE6A, PDE6B, PDE6C, PDE6G, PDE6H, PEX1, PEX2, PEX5, PEX6, PEX10, PEX12, PEX13, PEX26, PITPNM3, PLA2G5, PNPLA6, POC1B, POMGNT1, PRCD, PROM1, PRPF3, PRPF6, PRPF8, PRPF31, PRPH2, RAB28, RAX2, RBP3, RBP4, RD3, RDH5, RDH12, RGR, RGS9, RGS9BP, RHO, RIMS1, RLBP1, RP1, RP2, RP9, RPE65, RPGR, RPGRIP1, SAG, SEMA4A, SIX6, SLC24A1, SNRNP200, SPATA7, TEAD1, TOPORS, TRNT1, TRPM1, TSPAN12, TTC8, TTLL5, TULP1, UNC119, USH1C, USH1G, USH2A, VCAN, ZNF513.