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| Panel Name, Specifity and genes Tested/covered |
 Retinitis pigmentosa (NGS panel for 72 genes).
By CGC Genetics (Portugal).
RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, TUB, TULP1, USH2A, CLRN1, BEST1, ARL6, CA4, ADGRA3, PRPF31, KLHL7 , (...)
View the complete list with 52 more genes
RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, TUB, TULP1, USH2A, CLRN1, BEST1, ARL6, CA4, ADGRA3, PRPF31, KLHL7, PRPF6, RP1L1, ARL2BP, DHX38, PRPF8, PRPF3, PRPF4, NMNAT1, RDH11, IMPG2, RDH12, TTC8, SPATA7, DHDDS, CNGA1, CNGB1, EYS, TOPORS, CERKL, KIAA1549, GNPTG, CYP4V2, CRB1, CRX, FLVCR1, FAM161A, ZNF513, C8orf37, SNRNP200, ECM1, PRCD, ABCA4, PCARE, FSCN2, GUCA1B, IDH3B, IMPDH1, LRAT, MAK, MERTK, NEK2, NR2E3, NRL, PDE6A, PDE6B, PDE6G, PROM1, BBS1, RBP3, RBP4, PRPH2, RGR
Specificity
2 %
Genes
100 %
|
Retinitis pigmentosa, AR and X-linked (NGS panel for 53 genes).
By CGC Genetics (Portugal).
RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, BEST1, ADGRA3, RP1L1, ARL2BP, DHX38, NMNAT1, RDH11, IMPG2, RDH12, TTC8 , (...)
View the complete list with 33 more genes
RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, BEST1, ADGRA3, RP1L1, ARL2BP, DHX38, NMNAT1, RDH11, IMPG2, RDH12, TTC8, SPATA7, DHDDS, CNGA1, CNGB1, EYS, CERKL, KIAA1549, GNPTG, CYP4V2, CRB1, FLVCR1, FAM161A, ZNF513, C8orf37, EMC1, PRCD, ABCA4, PCARE, IDH3B, LRAT, MAK, MERTK, NEK2, NR2E3, NRL, PDE6A, PDE6B, PDE6G, PROM1, BBS1, RBP3, RBP4, RGR
Specificity
2 %
Genes
100 %
|
 Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1 , (...)
View the complete list with 286 more genes
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1, ACO2, TIMM8A, TIMP3, TREX1, CEP41, TTPA, TUB, TULP1, USH1C, CFAP410, USH2A, CLRN1, BEST1, WFS1, ARL6, RPGRIP1, CDH23, CA4, ADGRA3, CABP4, CACNA1F, PRDM13, IFT81, C1QTNF5, ELOVL4, TMEM237, CDHR1, PCDH15, CAPN5, OR2W3, PRPF31, KLHL7, PRPF6, KIZ, ABHD12, PANK2, RP1L1, DNAJC5, PNPLA6, USH1G, WHRN, TRIM32, TUBGCP4, ZNF423, MFN2, ADAMTS18, ARL2BP, DHX38, RIMS1, PRPF8, TRNT1, PRPF3, PRPF4, ADGRV1, CDH3, INVS, NMNAT1, RDH11, CEP83, MFRP, TUBGCP6, SLC4A5, RCBTB1, RAX2, WDR19, IMPG2, CEP250, IFT27, RTN4IP1, BBS7, CLUAP1, NPHP4, HMCN1, CHM, RD3, KCNV2, VSX2, KIAA0586, TTLL5, RDH12, ZNF408, TTC8, CACNA2D4, SPATA7, DHDDS, IFT88, TPP1, CLN3, CLN5, CLN6, CLN8, PITPNM3, INPP5E, CNGA1, CNGA3, CNGB1, CNGB3, EYS, AHI1, ADAM9, TSPAN12, TOPORS, CERKL, VPS13B, COL11A1, COL11A2, COL18A1, COL9A1, COL9A2, COL9A3, KIAA1549, PEX26, GNPTG, CYP4V2, ACBD5, CRB1, CRX, ADIPOR1, B9D1, CISD2, TCTN3, MMACHC, CIB2, VCAN, FLVCR1, LRIT3, TMEM216, CTNNA1, CTNNB1, NXNL1, SLC25A46, CTSD, TMEM126A, ARL13B, TTC21B, OFD1, CEP78, TCTN2, CPLANE1, FAM161A, TCTN1, AGBL5, CSPP1, PDZD7, BBS10, CFAP57, ZNF513, HGSNAT, BBS12, C12orf65, TMEM138, C8orf37, WDPCP, BBIP1, TMEM107, TMEM67, MFSD8, B9D2, DRAM2, IQCB1, EMC1, CEP290, IFT140, RPGRIP1L, CEP164, WDR35, CC2D2A, IFT80, SLC7A14, IFT43, BBS9, REEP6, RGS9BP, IFT172, KIF7, POC1B, SNRNP200, GPR179, MIR204, LCA5, EFEMP1, PRCD, ABCA4, PCARE, AIPL1, FBLN5, TMEM231, DTHD1, ISPD, FSCN2, FZD4, GDF6, ALMS1, GJB2, GJB6, GNAT1, GNAT2, AMACR, GRM6, GRN, GUCA1A, GUCA1B, GUCY2D, HARS, HCN1, CFH, HK1, HMX1, IDH3A, IDH3B, ABCC6, IMPDH1, IMPG1, ABCD1, ITM2B, JAG1, KCNJ13, KIF11, LAMA1, LARGE1, LRAT, LRP2, LRP5, LZTFL1, MAK, ARL3, MERTK, MKKS, MKS1, TRPM1, MTTP, MVK, MYO7A, NDP, NEK2, NEUROD1, NPHP1, NPHP3, ATF6, NR2E3, NR2F1, NRL, FRMD7, NYX, OAT, OPA1, OPA3, OTX2, PAX2, PCYT1A, PDE6A, PDE6B, PDE6C, PDE6D, PDE6G, PDE6H, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX3, PEX6, PEX7, PGK1, PHYH, PLA2G5, PPT1, PRKCG, PROM1, PRPS1, BBS1, BBS2, BBS4, BBS5, PEX19, PEX2, PEX5, RAB28, RBP3, RBP4, RDH5, PRPH2, RGR
Specificity
1 %
Genes
100 %
|
Comprehensive Monogenic Obesity Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
BDNF, SDCCAG8, SIM1, TUB, UCP3, KDM6A, ARL6, RAB23, TRIM32, PHF6, KSR2, IFT27, BBS7, TTC8, MRAP2, IFT74, VPS13B, CPE, CUL4B, BBS10 , (...)
View the complete list with 31 more genes
BDNF, SDCCAG8, SIM1, TUB, UCP3, KDM6A, ARL6, RAB23, TRIM32, PHF6, KSR2, IFT27, BBS7, TTC8, MRAP2, IFT74, VPS13B, CPE, CUL4B, BBS10, BBS12, C8orf37, WDPCP, BBIP1, TMEM67, CEP290, BBS9, SH2B1, DYRK1B, ALMS1, GNAS, MCHR1, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MKKS, MKS1, KMT2D, NR0B2, NTRK2, PCSK1, POMC, PPARG, BBS1, BBS2, BBS4, BBS5, RAI1
Specificity
2 %
Genes
100 %
|
 Retinitis pigmentosa, autosomal recessive and X-linked Panel.
By CeGaT GmbH (Germany).
RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, CLRN1, BEST1, ADGRA3, CDHR1, PRPF31, KIZ, RP1L1, ARL2BP, DHX38, NMNAT1 , (...)
View the complete list with 42 more genes
RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, CLRN1, BEST1, ADGRA3, CDHR1, PRPF31, KIZ, RP1L1, ARL2BP, DHX38, NMNAT1, RDH11, IMPG2, RDH12, ZNF408, TTC8, SPATA7, DHDDS, CNGA1, CNGB1, EYS, CERKL, KIAA1549, GNPTG, CYP4V2, CRB1, FLVCR1, FAM161A, ZNF513, HGSNAT, C8orf37, EMC1, SLC7A14, IFT172, PRCD, ABCA4, PCARE, IDH3B, LRAT, MAK, MERTK, NEK2, NR2E3, NRL, PDE6A, PDE6B, PDE6G, PROM1, BBS1, BBS2, RBP3, RBP4, RGR
Specificity
2 %
Genes
100 %
|
Retinal Dystrophy Panel.
By Molecular Vision Laboratory (United States).
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1 , (...)
View the complete list with 265 more genes
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1, ACO2, TIMM8A, TIMP3, TREX1, CEP41, TTPA, TUB, TULP1, USH1C, CFAP410, USH2A, CLRN1, BEST1, WFS1, ARL6, RPGRIP1, CDH23, CA4, ADGRA3, CABP4, CACNA1F, IFT81, C1QTNF5, ELOVL4, TMEM237, CDHR1, PCDH15, OR2W3, PRPF31, KLHL7, PRPF6, KIZ, ABHD12, PANK2, RP1L1, DNAJC5, PNPLA6, USH1G, WHRN, TRIM32, TUBGCP4, ZNF423, MFN2, ADAMTS18, ARL2BP, DHX38, RIMS1, PRPF8, TRNT1, PRPF3, PRPF4, ADGRV1, CDH3, INVS, NMNAT1, RDH11, MFRP, TUBGCP6, RAX2, WDR19, IMPG2, CEP250, IFT27, RTN4IP1, BBS7, NPHP4, HMCN1, CHM, RD3, KCNV2, TTLL5, RDH12, ZNF408, TTC8, CACNA2D4, SPATA7, DHDDS, TPP1, CLN3, CLN5, CLN6, CLN8, PITPNM3, INPP5E, CNGA1, CNGA3, CNGB1, CNGB3, EYS, AHI1, ADAM9, TSPAN12, TOPORS, CERKL, VPS13B, KCTD7, KIAA1549, PEX26, CYP4V2, ACBD5, CRB1, CRX, B9D1, CISD2, TCTN3, MMACHC, CIB2, VCAN, FLVCR1, LRIT3, TMEM216, CTNNA1, SLC25A46, CTSD, CTSF, RHEX, TMEM126A, ARL13B, TTC21B, OFD1, TCTN2, CPLANE1, FAM161A, TCTN1, CSPP1, PDZD7, BBS10, ZNF513, HGSNAT, BBS12, C12orf65, TMEM138, C8orf37, WDPCP, BBIP1, TMEM67, MFSD8, DGKQ, B9D2, DRAM2, IQCB1, EMC1, CEP290, IFT140, RPGRIP1L, CEP164, CC2D2A, SLC7A14, BBS9, RGS9BP, IFT172, KIF7, POC1B, SNRNP200, GPR179, MIR204, LCA5, EFEMP1, PRCD, ABCA4, PCARE, AIPL1, TMEM231, DTHD1, FSCN2, FZD4, OPN1MW, GDF6, ALMS1, GJB2, GJB6, GNAT1, GNAT2, AMACR, GRM6, GRN, GUCA1A, GUCA1B, GUCY2D, HARS, HCN1, CFH, HK1, HMX1, IDH3B, ABCC6, IMPDH1, IMPG1, ABCD1, ITM2B, JAG1, KCNJ13, KIF11, LAMA1, LRAT, LRP5, LZTFL1, MAK, ARL3, MERTK, MKKS, MKS1, TRPM1, MT-ND1, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MTTP, MT-TH, MT-TL1, MT-TV, MVK, MYO7A, NDP, NEK2, NEUROD1, NPHP1, NPHP3, ATF6, NR2E3, NR2F1, NRL, NYX, OAT, OPA1, OPA3, OTX2, PAX2, PDE6A, PDE6B, PDE6C, PDE6D, PDE6G, PDE6H, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX3, PEX6, PEX7, PGK1, PHYH, PLA2G5, PPT1, PROM1, PRPS1, BBS1, BBS2, BBS4, BBS5, PEX19, PEX2, PEX5, RAB28, RBP3, RBP4, OPN1LW, RDH5, PRPH2, RGR
Specificity
1 %
Genes
100 %
|
MVL Vision Panel.
By Molecular Vision Laboratory (United States).
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1 , (...)
View the complete list with 246 more genes
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1, TIMM8A, TIMP3, TREX1, CEP41, TTPA, TUB, TULP1, USH1C, CFAP410, USH2A, CLRN1, BEST1, WFS1, RPGRIP1, CDH23, CA4, ADGRA3, CABP4, CACNA1F, IFT81, C1QTNF5, ELOVL4, TMEM237, CDHR1, PCDH15, OR2W3, PRPF31, KLHL7, PRPF6, KIZ, PANK2, RP1L1, DNAJC5, PNPLA6, USH1G, WHRN, TRIM32, TUBGCP4, ZNF423, MFN2, DHX38, RIMS1, PRPF8, TRNT1, PRPF3, PRPF4, ADGRV1, CDH3, INVS, NMNAT1, RDH11, MFRP, TUBGCP6, RAX2, WDR19, IMPG2, CEP250, IFT27, RTN4IP1, BBS7, NPHP4, HMCN1, CHM, RD3, KCNV2, TTLL5, RDH12, ZNF408, TTC8, CACNA2D4, SPATA7, DHDDS, TPP1, CLN3, CLN5, CLN6, CLN8, PITPNM3, INPP5E, CNGA1, CNGA3, CNGB1, CNGB3, EYS, TSPAN12, TOPORS, CERKL, VPS13B, KCTD7, KIAA1549, PEX26, CYP4V2, CRB1, CRX, CISD2, TCTN3, MMACHC, CIB2, VCAN, FLVCR1, LRIT3, TMEM216, CTNNA1, SLC25A46, CTSD, CTSF, RHEX, TMEM126A, TTC21B, OFD1, TCTN2, CPLANE1, FAM161A, TCTN1, CSPP1, PDZD7, BBS10, ZNF513, HGSNAT, BBS12, C12orf65, TMEM138, C8orf37, WDPCP, BBIP1, TMEM67, MFSD8, DGKQ, DRAM2, IQCB1, EMC1, CEP290, IFT140, RPGRIP1L, CEP164, CC2D2A, SLC7A14, BBS9, RGS9BP, IFT172, KIF7, POC1B, SNRNP200, GPR179, MIR204, LCA5, EFEMP1, PRCD, PCARE, TMEM231, DTHD1, FSCN2, FZD4, OPN1MW, GDF6, GJB2, GJB6, GNAT1, GNAT2, GRM6, GRN, GUCA1A, GUCA1B, GUCY2D, HARS, HCN1, CFH, HK1, HMX1, IDH3B, IMPDH1, IMPG1, ITM2B, JAG1, KCNJ13, KIF11, LAMA1, LRAT, LRP5, LZTFL1, MAK, MERTK, MKKS, MKS1, TRPM1, MT-ND1, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MTTP, MT-TH, MT-TL1, MT-TV, MVK, MYO7A, NDP, NEK2, NEUROD1, NPHP1, NPHP3, NR2E3, NR2F1, NRL, NYX, OAT, OPA1, OPA3, OTX2, PAX2, PDE6A, PDE6B, PDE6C, PDE6D, PDE6G, PDE6H, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX3, PEX6, PEX7, PGK1, PHYH, PLA2G5, PPT1, PROM1, PRPS1, BBS1, BBS2, BBS4, BBS5, PEX19, PEX2, PEX5, RAB28, RBP3, RBP4, OPN1LW, RDH5, PRPH2, RGR
Specificity
1 %
Genes
100 %
|
TUB.
By Fulgent Genetics Fulgent Genetics (United States).
TUB
Specificity
100 %
Genes
100 %
|
You can check the following sources for additional information.
Retinal Dystrophy And Obesity; Rdob