Panel Name, Specifity and genes Tested/covered |
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis.
By Centogene AG - the Rare Disease Company in Germany.
PI4KA
Specificity
100 %
Genes
34 %
|
PI4KA.
By Fulgent Genetics Fulgent Genetics in United States.
PI4KA
Specificity
100 %
Genes
34 %
|
Epilepsy Advanced Sequencing and CNV Evaluation - Developmental Brain Malformations.
By Athena Diagnostics Inc in United States.
PAX6, CPT2, SHH, SLC25A19, TUBA1A, FGFR3, ARX, WDR62, FKTN, PEX7, POMGNT1, DPYD, FKRP, POMT2, POMT1, LAMA2, LARGE1, MCPH1, ASPM, FOLR1 , (...)
View the complete list with 20 more genes
PAX6, CPT2, SHH, SLC25A19, TUBA1A, FGFR3, ARX, WDR62, FKTN, PEX7, POMGNT1, DPYD, FKRP, POMT2, POMT1, LAMA2, LARGE1, MCPH1, ASPM, FOLR1, COL4A1, ARFGEF2, CENPJ, DEAF1, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B
Specificity
5 %
Genes
67 %
|
Epilepsy Advanced Sequencing and CNV Evaluation.
By Athena Diagnostics Inc in United States.
UBE3A, ALPL, ADSL, PAX6, CPT2, ATP6V0A2, HSD17B10, HPRT1, ADGRV1, SHH, POLG, SLC25A19, PANK2, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, SUCLA2 , (...)
View the complete list with 214 more genes
UBE3A, ALPL, ADSL, PAX6, CPT2, ATP6V0A2, HSD17B10, HPRT1, ADGRV1, SHH, POLG, SLC25A19, PANK2, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, SUCLA2, TUBA1A, CTSD, SLC25A22, ALG9, GRN, GLDC, AMT, SLC9A6, ALDH7A1, NDUFA1, L2HGDH, CYP27A1, TPP1, CLN3, WWOX, SLC6A8, FGFR3, ARX, CDKL5, CHRNA7, FOXG1, MEF2C, PCDH19, PLP1, RAI1, SLC2A1, WDR62, TSC2, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, GPC3, CLN6, CLN8, FKTN, PPT1, PEX7, POMGNT1, CLN5, PHGDH, PLA2G6, DPYD, CSTB, SCN1A, NOTCH3, FKRP, CACNA1A, KCNJ11, CASR, DYNC1H1, POMT2, POMT1, KCNA1, CACNB4, LAMA2, LARGE1, MCPH1, ASPM, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, EFHC1, CRH, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, KCNH2, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, SYNJ1, STX1B, SLC35A2, SLC6A1, FOLR1, GABRB2, GABRD, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, KCNC1, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, HCN4, LMNB2, MBD5, KCNMA1, SCARB2, SCN5A, SLC4A10, ALG13, ASAH1, TBC1D24, PRIMA1, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, COL4A1, ARFGEF2, CENPJ, DEAF1, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, CTSF, DNAJC5, MFSD8, ATP13A2, KMT2D, CACNA2D1, RBFOX1, CACNA2D2, MAGI2, HNRNPU, SETD2, TBL1XR1, SPATA5, EEF1A2, KCNA2, DNM1, SIK1, SNAP25, PURA, KCNB1, SLC13A5, DOCK7, NR2F1, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGN, PIGV, ANKRD11, PLCB1, SPTAN1, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, KIF1BP, SERPINI1, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, VPS13A, TBX1, LBR, ATP2A2
Specificity
1 %
Genes
67 %
|
NGS Epilepsy/Seizure Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.
MTHFR, UBE3A, ADSL, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, NDUFA1, TPP1, CLN3, ARX , (...)
View the complete list with 125 more genes
MTHFR, UBE3A, ADSL, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, NDUFA1, TPP1, CLN3, ARX, CDKL5, FOXG1, MEF2C, PCDH19, SLC2A1, WDR62, TSC2, SYNGAP1, TSC1, PTCH1, CLN6, CLN8, PPT1, CLN5, CSTB, SCN1A, CACNA1A, KCNJ11, CASR, KCNA1, CACNB4, MCPH1, ASPM, ATP1A2, CHRNB2, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, ST3GAL5, SCN1B, SCN2A, SYNJ1, SLC35A2, FOLR1, GABRD, GRIN2B, KCNT1, KCNQ2, KCNQ3, PNPO, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, SCARB2, SCN5A, TBC1D24, DEPDC5, PRRT2, ARFGEF2, CENPJ, DCX, EMX2, QARS, NDE1, SIX3, RELN, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, MFSD8, CACNA2D1, MAGI2, HNRNPU, SNAP25, SLC13A5, DOCK7, SZT2, ST3GAL3, KANSL1, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, IQSEC2, PHF6, ARHGEF9, SYN1, OPHN1, ATP6AP2, CASK, ZEB2, NECAP1, CCL2, CLCN2, NEDD4L, MTOR, VANGL1, KCNAB1, EXOSC3, TSEN34, TSEN2, TUBB2A, TGIF1, ZIC2, NALCN, CEP152, ABCB1, NODAL, FOXH1, CDON, GLI2, CDK5RAP2, FLVCR2, PCNT, ATR
Specificity
1 %
Genes
34 %
|
Comprehensive Brain Malformation Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.
UBE3A, PTEN, TUBB3, CC2D2A, OTX2, TMEM67, NPHP1, CEP290, SHH, SLC25A19, MECP2, TUBA1A, RARS2, MRPS16, SLC9A6, MKS1, SOX2, HESX1, ARX, CDKL5 , (...)
View the complete list with 86 more genes
UBE3A, PTEN, TUBB3, CC2D2A, OTX2, TMEM67, NPHP1, CEP290, SHH, SLC25A19, MECP2, TUBA1A, RARS2, MRPS16, SLC9A6, MKS1, SOX2, HESX1, ARX, CDKL5, DHCR7, FOXG1, WDR62, NIPBL, NSD1, PTCH1, FKTN, POMGNT1, TMEM216, AHI1, FKRP, FGF8, L1CAM, VRK1, POMT2, POMT1, LARGE1, MCPH1, ASPM, COL4A1, ARFGEF2, CENPJ, DCX, EMX2, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, KIF1BP, OFD1, ATRX, PHF6, OPHN1, CASK, CUL4B, ZEB2, ACTB, ACTG1, MED12, LAMC3, UPF3B, EXOSC3, TSEN34, TSEN2, TGIF1, ZIC2, CEP152, NODAL, FOXH1, CDON, GLI2, CDK5RAP2, PCNT, ATR, NFIX, EZH2, GLI3, RAB3GAP2, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, DLL1, EOMES, GAS1, PIK3CA, RAB18, IER3IP1, RBBP8, MYCN, VLDLR, DISP1
Specificity
2 %
Genes
67 %
|
Epilepsy/Seizure.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.
MTHFR, UBE3A, BTD, ADSL, MMACHC, ADGRV1, POLG, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, GLDC, AMT, SLC9A6, ALDH5A1, ALDH7A1 , (...)
View the complete list with 78 more genes
MTHFR, UBE3A, BTD, ADSL, MMACHC, ADGRV1, POLG, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, GLDC, AMT, SLC9A6, ALDH5A1, ALDH7A1, PTS, QDPR, TPP1, CLN3, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, SLC2A1, WDR62, TSC2, TSC1, CLN6, CLN8, PPT1, CLN5, PHGDH, CSTB, SCN1A, CACNA1A, GCH1, CASR, CACNB4, MCPH1, ASPM, ATP1A2, CHRNB2, CPA6, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, SCN1B, SCN2A, FOLR1, KCNQ2, KCNQ3, PNPO, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, TBC1D24, PRRT2, DCX, FLNA, TSEN54, PAFAH1B1, ADGRG1, DNAJC5, MFSD8, MAGI2, WDR45, SCN8A, NRXN1, PLCB1, SPTAN1, PNKP, KCNJ10, CNTNAP2, ARHGEF9, SYN1, OPHN1, CASK, ZEB2, PCBD1, PSPH
Specificity
2 %
Genes
34 %
|
Polymicrogyria Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, TUBA1A, WDR62, NDE1, RAB3GAP1, TUBA8, ADGRG1, TUBB2B, KIF1BP, GPSM2, RAB3GAP2, RAB18, OCLN, CCND2, AKT3-IT1, TBC1D20, RTTN
Specificity
6 %
Genes
34 %
|
GPR56 sequencing.
By Genetic Services Laboratory University of Chicago in United States.
ADGRG1
Specificity
100 %
Genes
34 %
|
Cerebral Cortical Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, POMT2, POMT1, LARGE1, DCX, RAB3GAP1, RELN, TUBA8, PAFAH1B1, ADGRG1, TUBB2B, KIF1BP, ACTB, ACTG1 , (...)
View the complete list with 6 more genes
TUBB3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, POMT2, POMT1, LARGE1, DCX, RAB3GAP1, RELN, TUBA8, PAFAH1B1, ADGRG1, TUBB2B, KIF1BP, ACTB, ACTG1, LAMC3, RAB3GAP2, RAB18, VLDLR, OCLN, RTTN
Specificity
4 %
Genes
34 %
|
Cerebral Cortical Malformation Sequencing Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1 , (...)
View the complete list with 34 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1, RAB3GAP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, TUBB2B, KIF1BP, ACTB, ACTG1, LAMC3, TUBB2A, GPSM2, POMK, GMPPB, TUBB4A, RAB3GAP2, RAB18, VLDLR, AKT3, OCLN, CCND2, TBC1D20, RTTN, B3GNT2, CDK5, KATNB1, TUBG1, TUBB, KIF5C, KIF2A, ERMARD, ASNS, SNAP29
Specificity
2 %
Genes
34 %
|
Lissencephaly Sequencing Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, DCX, NDE1 , (...)
View the complete list with 16 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, DCX, NDE1, RELN, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, POMK, GMPPB, VLDLR, CDK5, KATNB1, TUBG1, TUBB, KIF5C, SNAP29, LAMB1
Specificity
3 %
Genes
34 %
|
GPR56 deletion/duplication analysis.
By Genetic Services Laboratory University of Chicago in United States.
ADGRG1
Specificity
100 %
Genes
34 %
|
Polymicrogyria Sequencing Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, TUBA1A, WDR62, NDE1, RAB3GAP1, TUBA8, ADGRG1, TUBB2B, KIF1BP, GPSM2, RAB3GAP2, RAB18, OCLN, CCND2, AKT3-IT1, TBC1D20, RTTN
Specificity
6 %
Genes
34 %
|
Comprehensive Lissencephaly Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, RXYLT1, LARGE1, B3GALNT2, DCX, RELN, PAFAH1B1 , (...)
View the complete list with 14 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, RXYLT1, LARGE1, B3GALNT2, DCX, RELN, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, POMK, GMPPB, VLDLR, CDK5, KATNB1, TUBG1, TUBB, KIF5C, SNAP29, LAMB1
Specificity
3 %
Genes
34 %
|
Cerebral Cortical Malformations Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1 , (...)
View the complete list with 34 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1, RAB3GAP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, TUBB2B, KIF1BP, ACTB, ACTG1, LAMC3, TUBB2A, GPSM2, POMK, GMPPB, TUBB4A, RAB3GAP2, RAB18, VLDLR, AKT3, OCLN, CCND2, TBC1D20, RTTN, B3GNT2, CDK5, KATNB1, TUBG1, TUBB, KIF5C, KIF2A, ERMARD, ASNS, SNAP29
Specificity
2 %
Genes
34 %
|
Ataxia Exome Panel.
By Genetic Services Laboratory University of Chicago in United States.
FMR1, TTR, UBE3A, AARS2, ABHD12, PC, UQCRQ, UQCRB, HLCS, BTD, ATP7B, ATPAF2, AUH, BCKDHA, BCKDHB, BCS1L, TWNK, C12orf65, ADSL, PRKCG , (...)
View the complete list with 460 more genes
FMR1, TTR, UBE3A, AARS2, ABHD12, PC, UQCRQ, UQCRB, HLCS, BTD, ATP7B, ATPAF2, AUH, BCKDHA, BCKDHB, BCS1L, TWNK, C12orf65, ADSL, PRKCG, PAX6, PSEN1, INPP5E, AMACR, HSD17B4, CPS1, OPA1, WFS1, PSAP, GLB1, CC2D2A, ELOVL4, TMEM67, NPHP1, CEP290, DLD, POLG, NDUFS4, HSPD1, AFG3L2, FOXRED1, RRM2B, NDUFAF2, KIF1B, PANK2, OPA3, MECP2, COQ9, PDSS2, PDSS1, COQ6, ACO2, NDUFA12, HARS, NDUFB3, NDUFA9, COX14, ALDH18A1, PDHB, TMEM70, NDUFAF1, TTC19, MTPAP, NDUFA10, NUBPL, GPI, GAMT, SPR, STXBP1, COQ8A, RFT1, TUBA1A, RARS2, DARS2, TSFM, REEP1, DNAJC19, CTSD, MPDU1, FLVCR1, DPM1, GRN, COQ2, SPG7, ALG6, TYMP, ETHE1, SQSTM1, OTC, PDHA1, ABCB7, SLC9A6, ABCD1, MMADHC, TCN2, HEXA, SUOX, ALDH5A1, HEXB, PHYH, PTS, MPV17, CTSA, NDUFA2, COX15, SURF1, NDUFS8, NDUFS7, NDUFS3, NDUFAF6, SDHAF1, NDUFAF3, NDUFA1, NDUFA11, NDUFAF4, NDUFS1, NDUFV1, NDUFV2, NDUFS6, NDUFS2, NDUFAF5, HIBCH, DBT, SUCLG1, DLAT, GALC, L2HGDH, GBE1, FXN, LRPPRC, FASTKD2, COX6B1, ASS1, CYP27A1, PMM2, MKS1, APTX, ASL, TPP1, WWOX, PNKD, SOD1, TACO1, FARS2, MTFMT, SDHA, PNP, ARSA, CDKL5, EIF2B1, FOXG1, GJC2, NPC1, NPC2, PCDH19, PLP1, SLC2A1, TINF2, WDR62, ATM, MRE11, NF2, SDHD, PRF1, CLN6, CLN8, FKTN, PEX2, PPT1, PEX7, SACS, TH, MLC1, PEX1, POMGNT1, SLC17A5, SUMF1, TTPA, CLN5, EIF2B5, PLA2G6, TMEM216, PRX, SH3TC2, MPZ, PMP22, EGR2, DNM2, GJB1, ATL1, ZFYVE26, EIF2B3, EIF2B2, EIF2B4, SPG11, CSTB, SCN1A, AHI1, FKRP, CACNA1A, GCH1, SPAST, KIF5A, L1CAM, NIPA1, SLC33A1, BSCL2, RTN2, PNPLA6, KIF1A, CYP7B1, AP5Z1, FA2H, SPART, SPG21, ALS2, SETX, DYNC1H1, VRK1, SYNE1, TRAPPC11, POMT2, POMT1, ISPD, KCNA1, CACNB4, SLC1A3, SYT14, ANO10, TDP1, SIL1, GRM1, VAMP1, EEF2, KCND3, KCNC3, ITPR1, PDYN, FGF14, TGM6, TTBK2, SPTBN2, POMGNT2, LARGE1, ATP1A2, ATP1A3, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SLC19A3, SCN2A, SLC6A1, FOLR1, HCN1, KCNQ2, KCNC1, EPM2A, LMNB2, MBD5, SCARB2, TBC1D24, PRRT2, BRAT1, DCX, RELN, TSEN54, ADGRG1, CTSF, DNAJC5, MFSD8, ATP13A2, KCNA2, SNAP25, SLC13A5, ROGDI, SCN8A, SPTAN1, PNKP, KCNJ10, TCF4, OFD1, OPHN1, CASK, CUL4B, GFAP, HTRA1, CLPP, ERCC3, POLR1C, DNMT1, SOX10, SLC19A2, PRPS1, AP1S2, KIAA0586, PEX16, PEX26, PEX10, MVK, NEU1, DKC1, SLC16A2, CLCN2, EXOSC3, TSEN34, TSEN2, NALCN, MME, LRSAM1, GAN, IFT140, CAV1, NKX2-1, FBXL4, GMPPB, PIEZO2, CHMP1A, ERCC6, ERLIN1, KIDINS220, CAPN1, HACE1, MAG, CPT1C, ENTPD1, NT5C2, KIF1C, C19orf12, UCHL1, B4GALNT1, TUBB4A, GBA2, CYP2U1, DDHD2, TECPR2, DDHD1, ERLIN2, AP4S1, AP4B1, AP4E1, AP4M1, CTDP1, PGK1, HNRNPH2, RNASET2, CTC1, GJA1, FTL, CP, ERCC4, B9D1, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, EOMES, VLDLR, MARS2, COX10, SCO1, MT-TP, COG4, PRNP, SLC46A1, TPK1, SLC20A2, APOB, ERCC8, LIG4, GCLC, GSS, SLC39A4, ADA2, SLC25A46, PGM3, TCTN3, SAMD9L, KIAA0556, CEP104, CEP120, TMEM107, PDE6D, CSPP1, HERC1, HEPACAM, DNAJC3, LRP4, TUBB, IBA57, ARL6IP1, CCDC88C, CA8, ZIC1, XRCC4, SEPSECS, TBCE, COX20, MECR, UBA5, NUP62, AAAS, NAXE, RARS, ATP8A2, ATP2B3, CTBP1, CACNA1G, CAMTA1, BEAN1, ATCAY, DOCK3, COL18A1, EBF3, SLC52A2, LAMA1, GRID2, NOL3, PIK3R5, PCNA, DMXL2, PTRH2, ELOVL5, RTN4IP1, RNASEH1, RNF216, SCYL1, ERCC5, RNF168, SLC6A19, TELO2, TRPC3, TDP2, VARS, ZIC4, NAT8L, OTUD4, PUM1, STUB1, ARV1, DGAT2, FGF12, ITM2B, LMNB1, YME1L1, MAPK10, SLC9A1, SLC52A3, COQ4, RUBCN, PMPCA, UROC1, TRNT1, XPA, ZNF592, COA5, WDR81, POLR3A, POLR3B, RNF170, PET100, PRDM8, CHCHD10, APOPT1, SNX14, TMEM240, WDR73, CWF19L1, VWA3B, THG1L, CHAMP1, PIGG
Specificity
1 %
Genes
34 %
|
GPR56.
By Institute for Human Genetics University Clinic Freiburg in Germany.
ADGRG1
Specificity
100 %
Genes
34 %
|
Comprehensive Brain Malformations Panel.
By GeneDx in United States.
TUBB3, INPP5E, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2 , (...)
View the complete list with 24 more genes
TUBB3, INPP5E, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2, DCX, NDE1, PQBP1, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, OPHN1, CASK, LAMC3, TSEN34, TSEN2, TMEM237, TMEM138, RPGRIP1L, KIF7, CEP41, EOMES, VLDLR, OCLN
Specificity
5 %
Genes
67 %
|
Cortical Brain Malformations Panel.
By GeneDx in United States.
TUBB3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, POMT2, POMT1, LARGE1, ARFGEF2, DCX, NDE1, PQBP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, SRPX2, TUBB2B , (...)
View the complete list with 4 more genes
TUBB3, TUBA1A, ARX, FKTN, POMGNT1, FKRP, POMT2, POMT1, LARGE1, ARFGEF2, DCX, NDE1, PQBP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, LAMC3, EOMES, VLDLR, OCLN
Specificity
9 %
Genes
67 %
|
GPR56. Complete sequencing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.
ADGRG1
Specificity
100 %
Genes
34 %
|
Polymicrogyria, bilateral frontoparietal (sequence analysis of GPR56 gene).
By CGC Genetics in Portugal.
ADGRG1
Specificity
100 %
Genes
34 %
|
Bilateral frontoparietal polymicrogyria (BFPP) via ADGRG1 (GPR56) Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics in United States.
ADGRG1
Specificity
100 %
Genes
34 %
|
Leukodystrophy and Leukoencephalopathy Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics in United States.
PC, TYROBP, ATP7A, ATP7B, TWNK, ADSL, HSD17B4, CPS1, PSAP, GLB1, OCRL, POLG, NDUFS4, HSPD1, SLC25A4, RRM2B, FH, COQ9, DNM1L, DGUOK , (...)
View the complete list with 134 more genes
PC, TYROBP, ATP7A, ATP7B, TWNK, ADSL, HSD17B4, CPS1, PSAP, GLB1, OCRL, POLG, NDUFS4, HSPD1, SLC25A4, RRM2B, FH, COQ9, DNM1L, DGUOK, BOLA3, NFU1, HMGCL, NUBPL, SCP2, IDH2, SLC25A12, SDHB, SUCLA2, MRPS22, DARS2, TUFM, GFM1, COQ2, SPG7, TYMP, D2HGDH, OTC, ABCD1, HEXA, ALDH5A1, ALDH3A2, ACOX1, PAH, TCIRG1, COX15, SURF1, NDUFS8, MOCS1, SDHAF1, NDUFS1, NDUFV1, NDUFS2, GALC, L2HGDH, GBE1, ETFB, ETFA, ETFDH, GCDH, GALT, CYP27A1, FARS2, MTFMT, AGA, ARSA, ASPA, EIF2B1, GJC2, GLA, IDS, IKBKG, NPC1, NPC2, PLP1, PEX2, PPT1, MLC1, MCOLN1, PEX1, SLC17A5, SUMF1, EIF2B5, GJB1, ZFYVE26, EIF2B3, EIF2B2, EIF2B4, SPG11, NOTCH3, CYP7B1, FA2H, SPART, DAG1, SLC19A3, FOLR1, COL4A1, ADGRG1, SAMHD1, RNASEH2A, RNASEH2C, RNASEH2B, TREX1, GFAP, HTRA1, CLPP, POLR1C, SOX10, PEX6, FUCA1, PEX14, PEX19, PEX13, PEX3, PEX16, PEX26, PEX10, PEX12, PEX5, SLC16A2, CLCN2, GAN, ERCC6, TUBB4A, CYP2U1, ADAR, RNASET2, CTC1, GJA1, DCAF17, MARS2, COX10, CSF1R, TREM2, EARS2, ERCC8, OCLN, HEPACAM, IBA57, SLC25A1, BCAP31, RARS, LMNB1, POLR3A, POLR3B, APOPT1, FAM126A, COL4A2, PEX11B, AIMP1, DARS, LYRM7, JAM3, ISCA2
Specificity
1 %
Genes
34 %
|
Lissencephaly and related disorders NGS test.
By Connective Tissue Gene Tests in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2 , (...)
View the complete list with 22 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, DCX, NDE1, RELN, TUBA8, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, TUBB2A, POMK, GMPPB, VLDLR, CDK5, KATNB1, TUBG1, TUBB, KIF5C, KIF2A, SNAP29, LAMB1, TMTC3
Specificity
3 %
Genes
34 %
|
Lissencephaly and related disorders Deletion / Duplication test.
By Connective Tissue Gene Tests in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2 , (...)
View the complete list with 22 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, DCX, NDE1, RELN, TUBA8, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, TUBB2A, POMK, GMPPB, VLDLR, CDK5, KATNB1, TUBG1, TUBB, KIF5C, KIF2A, SNAP29, LAMB1, TMTC3
Specificity
3 %
Genes
34 %
|
Lissencephaly and related disorders Comprehensive test.
By Connective Tissue Gene Tests in United States.
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2 , (...)
View the complete list with 22 more genes
TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, DAG1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, DCX, NDE1, RELN, TUBA8, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, TUBB2A, POMK, GMPPB, VLDLR, CDK5, KATNB1, TUBG1, TUBB, KIF5C, KIF2A, SNAP29, LAMB1, TMTC3
Specificity
3 %
Genes
34 %
|
Mental retardation - different panels.
By Institute of Human Genetics Cologne University in Germany.
FMR1, UBE3A, PTEN, MCCC1, MCCC2, ACAD9, PC, ANKH, HLCS, ATP7A, AUH, B4GALT7, BCKDHA, BCKDHB, BCS1L, C12orf65, ADSL, MMACHC, PRKCG, PAX6 , (...)
View the complete list with 847 more genes
FMR1, UBE3A, PTEN, MCCC1, MCCC2, ACAD9, PC, ANKH, HLCS, ATP7A, AUH, B4GALT7, BCKDHA, BCKDHB, BCS1L, C12orf65, ADSL, MMACHC, PRKCG, PAX6, MTR, INPP5E, MTRR, PYCR1, CC2D2A, PRODH, ATP6V0A2, SRD5A3, HSD17B10, OCRL, ELOVL4, NDP, OTX2, HPRT1, NHS, TMEM67, ARL6, NPHP1, MKKS, CEP290, TTC8, TRIM32, SHH, DLD, NDUFS4, PANK2, RAF1, FH, SMPD1, MECP2, PDSS2, PDSS1, ACO2, NDUFA12, DDOST, ALDH18A1, DNM1L, ACSF3, CCDC28B, TAT, NUBPL, DPM3, PGM1, GAMT, GATM, AK1, SDHB, STXBP1, COQ8A, RFT1, MRPS22, TUBA1A, COG1, COG8, DARS2, TUSC3, HAX1, DNAJC19, CTSD, SLC25A22, MPDU1, DPM1, COG7, ALG9, ALG1, AP3B1, ALG8, ALG2, GRN, COQ2, ALG12, B4GALT1, GCSH, GLDC, AMT, SCO2, SLC35A1, GAD1, ALG6, MPI, ETHE1, STRA6, ALG3, D2HGDH, PUS1, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, MMADHC, ABHD5, SUOX, ALDH5A1, ALDH3A2, SLC35C1, ACOX1, CA2, COX15, SURF1, NDUFS8, NDUFS7, NDUFS3, GUSB, GNS, HGSNAT, NAGLU, SGSH, MOCS2, MOCS1, NDUFA1, NDUFA11, NDUFS1, NDUFV1, NDUFS2, NDUFAF5, MMAA, MUT, CYB5R3, DBT, MANBA, MAN2B1, MLYCD, SLC25A15, L2HGDH, CBS, GALT, GALE, LRPPRC, MGAT2, PMM2, BBS7, BBS5, BBS12, MKS1, BBS9, BBS10, BBS4, BBS1, BBS2, APTX, ASL, SOX2, TPP1, CLN3, HESX1, PPOX, WWOX, FARS2, SLC6A8, PDHX, SDHA, ABCD4, AGA, AHCY, DOLK, DPAGT1, MOGS, HPD, MGME1, PNP, FGFR3, ASPA, ARX, BLM, BRAF, CDKL5, CHD7, CREBBP, DHCR7, DMD, FOXG1, GJC2, HRAS, IDS, IDUA, IKBKG, KRAS, MAP2K1, MEF2C, DMPK, NRAS, PCDH19, PLP1, PORCN, PTPN11, RAI1, RMRP, SHOC2, SLC2A1, SOS1, WDR62, FGFR2, SOS2, HDAC8, RIT1, MAP2K2, TSC2, RAD21, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, NBN, PTCH1, GPC3, SMAD4, CLN6, CLN8, FKTN, PPT1, PEX7, SLC35A3, TH, MCOLN1, PEX1, POMGNT1, SLC12A6, SLC17A5, CLN5, PHGDH, DPYD, TMEM216, FIG4, NTRK1, MT-TL1, ZFYVE26, MT-TK, MT-ATP6, SPG11, SCN1A, AHI1, FKRP, ATXN10, GCH1, NF1, FGFR1, KCNJ11, L1CAM, SLC33A1, BSCL2, WASHC5, KIF1A, SPART, CCDC78, DYNC1H1, VRK1, TRAPPC11, DAG1, POMT2, POMT1, ISPD, ANO10, SIL1, GRM1, LAMA2, DPM2, POMGNT2, CHKB, LARGE1, B3GALNT2, MCPH1, ASPM, ATP1A2, ATP1A3, GABRB3, KCTD7, ST3GAL5, SCN2A, SLC35A2, SLC6A1, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, CHD2, GABRA1, GRIN2A, MBD5, ALG13, ASAH1, TBC1D24, PRIMA1, DEPDC5, PRRT2, BRAT1, PIGO, COL4A1, ARFGEF2, CENPJ, DEAF1, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, STIL, TUBB2B, CTSF, DNAJC5, MFSD8, ATP13A2, KMT2D, CACNA2D2, SETD2, TBL1XR1, SPATA5, EEF1A2, KCNA2, DNM1, SIK1, PURA, KCNB1, SLC13A5, DOCK7, NR2F1, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGN, PIGV, ANKRD11, PLCB1, SPTAN1, PNKP, SAMHD1, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, KIF1BP, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, ATP2A2, SHANK3, SHANK2, SALL1, ACTB, ACTG1, ATP6V1B2, ERCC2, ERCC3, PNPT1, NLRP3, DIAPH1, SOX10, MT-TS1, PRPS1, PEX6, NARS2, FUCA1, PTCHD1, ADNP, MID1, MED12, LAMC3, FOXP1, EHMT1, CACNA1C, AP1S2, CHD8, HOXA1, TBR1, TMEM231, ARID1B, CTNNB1, NLGN4X, NLGN3, LZTR1, KIAA0586, PEX13, PEX26, PEX10, PEX12, PEX5, KAT6B, MVK, NEU1, CCBE1, PHF8, HUWE1, HCFC1, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, USP9X, ZC4H2, GDI1, FTSJ1, RPS6KA3, SHROOM4, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, LAS1L, EIF2S3, FRMPD4, CLCN4, CCDC22, CNKSR2, THOC2, SPRED1, NSUN2, RASA2, RRAS, NECAP1, MTOR, EXOSC3, TUBB2A, TGIF1, ZIC2, NALCN, CEP152, CDON, GLI2, CDK5RAP2, PCNT, ATR, NAGA, DYM, TGFBR1, TGFBR2, SKI, ACVR1, DNMT3A, NFIX, EZH2, GLI3, ABCC9, MAGEL2, KDM6A, DHTKD1, AARS, MED25, POC1B, MAF, SLC4A4, NKX2-1, EMC1, FBXL4, POMK, GMPPB, LZTFL1, IFT27, BBIP1, WDPCP, SDCCAG8, ERCC6, ARID2, SMARCE1, KMT2A, SMARCA4, SMARCB1, ARID1A, SMARCA2, HACE1, MAG, IFIH1, PGAP1, ENTPD1, NT5C2, B4GALNT1, TUBB4A, GBA2, CYP2U1, DDHD2, TECPR2, ADAR, VPS37A, ERLIN2, RAB3GAP2, AP4S1, AP4B1, AP4E1, AP4M1, STAMBP, KIF11, CTDP1, PGK1, MT-CO2, MT-ND5, MT-CO1, MT-CO3, DPP6, THRB, EP300, RNASET2, EFTUD2, ASXL1, GNPAT, GNAS, WNT1, FANCD2, SOX5, SATB2, KATNAL2, AUTS2, MASP1, ERCC4, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, PIK3CA, RAB18, IER3IP1, RBBP8, MYCN, VLDLR, COX10, MT-TV, COG4, ALG11, COG6, COG5, TMEM165, MAT1A, EARS2, DDC, SLC6A3, EIF2AK3, DHCR24, MYO5A, RAB27A, STIM1, RARB, B3GLCT, PIK3R2, AKT3, ERCC8, LIG4, TPI1, GSS, PRKRA, EPG5, PIK3R1, PACS1, PGM3, TCTN3, MICU1, UBR1, OCLN, KCNJ6, AGPAT2, IFT172, PRMT7, AFF4, SRCAP, KIAA0556, CEP104, PDE6D, CSPP1, KPTN, RNF125, TBC1D7, HEPACAM, TRMT10A, ZBTB20, ZNF423, CEP83, TBC1D20, RTTN, ESCO2, DNMT3B, FRAS1, CDK5, KATNB1, TUBG1, KIF5C, KIF2A, ASNS, SNAP29, PDE4D, PTDSS1, CCDC88C, MPDZ, LAMB1, SLC25A1, MED17, MFSD2A, CENPE, CDK6, CEP135, CEP63, ZMYND11, TTI2, TAF2, SLC6A17, SETD5, NDST1, MID2, METTL23, KIF4A, FMN2, FBXO31, CRADD, ADAT3, GATAD2B, CTCF, ANK3, TECR, MED23, LRP2, LINS1, C12orf57, SOBP, CDH15, ZNF526, ZC3H14, TRAPPC9, PRSS12, MAN1B1, GRIK2, CRBN, CC2D1A, CA8, DPH1, MEGF8, TCF12, ORC1, GMNN, PLK4, LARP7, POC1A, PYCR2, TUBGCP4, ASXL3, TUBGCP6, TBCE, PPP1R15B, SLC1A4, SERAC1, CLPB, KMT2B, BCAP31, ACY1, CACNA1G, COL18A1, LAMA1, PTRH2, SCYL1, ERCC5, COQ4, PMPCA, XPA, WDR81, POLR3A, POLR3B, PET100, APOPT1, SNX14, WDR73, CHAMP1, PIGG, ZSWIM6, BUB1B, AP1S1, MPLKIP, GTF2H5, CA5A, PEPD, FAM126A, DHFR, COL4A2, PEX11B, POGZ, DDX3X, KAT6A, IGF1, COLEC11, HDAC4, SLC12A5, PIGT, RBM28, GPHN, SSR4, UBE3B, AIMP1, STT3B, STT3A, TMCO1, ERCC1, FTO, CLP1, HMGB3, MAB21L2, SMOC1, RNF113A, MFF, FAR1, SC5D, UNC80, UPB1, NECTIN1, CAD, KCNH1, RLIM, KLHL15, USP27X, DARS, DDX59, KDM1A, JAM3, ISCA2, ELP2, TRIO, MED13L, MYT1L, DCPS, TRIP12, TCF20, GABBR2, PPP2R1A, FASN, SNX27, ITPA, RMND1, SFXN4, RSPRY1, GTF2E2, APC2, HNRNPK, HIST1H4B, GON4L, SLC39A6, SCAPER, ADRA2B, KRBOX4, CCNA2, KDM6B, MEIS2, PGAP3, PECR, CKAP2L, CASP2, FRMD4A, GEMIN4, INPP4A, ZCCHC8, HIKESHI, SLC25A16, RABL6, TMEM135, GPT2, ASCC3, HIST3H3, CNKSR1, WAC, KDM5A, ACBD6, CCDC88A, AHDC1, TM4SF20, HERC2, SETD1A, KCNK9, ZBTB40, RALGDS, IMPA1, TANGO2, GMPPA, PGAP2, TRMT1, SLC31A1, CAPN10, PARP1, UBR7, EEF1B2, DIP2B, WDR45B, CCDC115, ADK, COL4A3BP, RGS7, FRY, EXOSC2, PPP2R5D, PRMT9
Specificity
1 %
Genes
34 %
|
Brain Malformations / Neuronal Migration Disorders.
By MGZ Medical Genetics Center in Germany.
FMR1, UBE3A, PTEN, APP, TUBB3, HSD17B10, HPRT1, PANK2, FH, MECP2, GAMT, STXBP1, TUBA1A, SLC25A22, GLDC, GK, MAOA, ACSL4, SLC9A6, ALDH7A1 , (...)
View the complete list with 246 more genes
FMR1, UBE3A, PTEN, APP, TUBB3, HSD17B10, HPRT1, PANK2, FH, MECP2, GAMT, STXBP1, TUBA1A, SLC25A22, GLDC, GK, MAOA, ACSL4, SLC9A6, ALDH7A1, HGSNAT, SGSH, GALC, CYP27A1, TPP1, CLN3, FGFR3, ASPA, ARX, ELP1, CDKL5, CHD7, FOXG1, IDS, MEF2C, PCDH19, PORCN, SLC2A1, WDR62, HDAC8, TSC2, RAD21, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, PTCH1, CDKN1C, GPC3, CLN6, DOK7, PPT1, MLC1, CLN5, EIF2B5, PHGDH, PLA2G6, EIF2B3, CSTB, SCN1A, NOTCH3, SGCE, FGF8, CASR, L1CAM, FA2H, CACNB4, ASPM, CACNA1H, CHRNB2, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN1B, SCN2A, SYNJ1, GABRD, HCN1, KCNT1, KCNQ2, KCNQ3, PNPO, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, SCARB2, ASAH1, TBC1D24, DEPDC5, PRRT2, COL4A1, ARFGEF2, CENPJ, DCX, QARS, NDE1, PQBP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, ATP13A2, SETD2, EEF1A2, NEXMIF, WDR45, SCN8A, NRXN1, DYRK1A, PLCB1, SPTAN1, PNKP, SAMHD1, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, KIF1BP, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, ZEB2, TREX1, VPS13A, HTRA1, PTCHD1, MID1, MED12, EHMT1, AP1S2, CHD8, ARID1B, NLGN4X, NLGN3, NEU1, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, EIF2S3, ZMYM3, CLCN4, THOC2, EXOSC3, TUBB2A, CEP152, NODAL, FOXH1, CDON, GLI2, CDK5RAP2, NFIX, EZH2, RNF135, GLI3, GPSM2, KDM6A, HNRNPDL, MYBPC1, SMARCE1, SMARCA4, SMARCB1, ARID1A, SMARCA2, C19orf12, TUBB4A, ADAR, PGK1, FTL, CP, DCAF17, KIF7, EOMES, PIK3CA, DISP1, GNAQ, PIK3R2, AKT3, AKT1, XK, TDGF1, ADA2, OCLN, KPTN, TBC1D7, HEPACAM, CCND2, TUBG1, TUBB, KIF5C, KIF2A, ZNF674, KCNH5, SEPSECS, NOL3, STUB1, ITM2B, POLR3A, POLR3B, COL4A2, DIS3L2, CLP1, DARS, JAM3, ARHGEF15, HERC2, NXF5
Specificity
1 %
Genes
67 %
|
Polymicrogyria.
By MGZ Medical Genetics Center in Germany.
TUBB3, FH, TUBA1A, CHD7, WDR62, NDE1, TUBA8, ADGRG1, SRPX2, TUBB2B, KIF1BP, NSDHL, GPSM2, EOMES, OCLN, TUBB, KIF5C
Specificity
12 %
Genes
67 %
|
Polymicrogyria, bilateral frontoparietal.
By Centogene AG - the Rare Disease Company in Germany.
ADGRG1
Specificity
100 %
Genes
34 %
|
AllNeuro panel.
By Centogene AG - the Rare Disease Company in Germany.
F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)
View the complete list with 1185 more genes
F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, PC, UQCRQ, ARG1, UQCRB, TYROBP, ATP5F1E, ATP7A, ATP7B, ATPAF2, BCKDHA, BCKDHB, BCS1L, BEST1, TWNK, C12orf65, GAA, ADSL, MMACHC, FBLN5, PRKCG, APP, AMN, PAX6, TGFB1, PSEN1, TUBB3, MTR, RET, OPTN, GPR143, INPP5E, MTRR, AMACR, HSD17B4, CPT2, OPA1, KRT5, DTNBP1, WFS1, PSAP, GLB1, CC2D2A, ATP6V0A2, SRD5A3, GNE, HSD17B10, OCRL, ELOVL4, NDP, HPRT1, NHS, TMEM67, ARL6, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, TTC8, TRIM32, SHH, PRPH2, AASS, DLD, POLG, NDUFS4, HSPD1, SLC25A19, SLC25A4, GARS, AFG3L2, FOXRED1, RRM2B, NDUFAF2, KIF1B, MFN2, CRYAB, PANK2, HADHA, RAF1, OPA3, FH, VCP, SMPD1, MECP2, CYP11B2, MTO1, COQ9, PDSS2, PDSS1, ACO2, NDUFA12, DDOST, NDUFB3, NDUFA9, AGK, ALDH18A1, HPS1, DNM1L, DGUOK, BOLA3, ACSF3, BLOC1S3, HPS6, HPS5, HPS4, HPS3, TMEM70, NFU1, PCK2, NDUFAF1, CCDC28B, TTC19, MTPAP, NDUFA10, NUBPL, SCP2, KARS, SPTLC2, ABAT, GFER, TLR3, TMEM126A, SLC25A12, DPM3, PGM1, LDHA, ENO3, GAMT, GATM, SPR, STXBP1, SUCLA2, COQ8A, RFT1, TUBA1A, GYS1, RARS2, COG1, COG8, DARS2, TUSC3, SLC25A3, PNPLA2, TSFM, HTRA2, REEP1, DNAJC19, POLG2, CTSD, ACADSB, TK2, SLC25A22, MPDU1, GFM1, FLVCR1, HADHB, DPM1, COG7, ALG9, ATIC, ALG1, AP3B1, ALG8, ALG2, GRN, COQ2, SPG7, ALG12, B4GALT1, PARK7, HMGCS2, PINK1, GCSH, GLDC, AMT, CISD2, SCO2, SLC35A1, GAD1, ALG6, TYMP, MPI, ETHE1, ALG3, PUS1, OTC, FRMD7, HCCS, PDHA1, GK, TIMM8A, TAZ, ABCB7, AIFM1, MAOA, PHKA1, ACSL4, SLC9A6, BCOR, ABCD1, MMADHC, LMBRD1, ABHD5, HEXA, GM2A, ALDH5A1, ALDH3A2, HEXB, LPIN1, PHYH, SLC35C1, ALDH7A1, ACOX1, PGAM2, PTS, QDPR, PAH, AGXT, MPV17, NDUFA2, COX15, SURF1, NDUFS8, NDUFS7, NDUFS3, NDUFAF6, CHAT, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, SDHAF1, NDUFAF3, NDUFA1, NDUFA11, NDUFAF4, NDUFS1, NDUFV1, NDUFV2, NDUFS6, NDUFS2, NDUFAF5, MCEE, MMAB, MMAA, MUT, DBT, SUCLG1, GALC, ALDH4A1, HK1, PFKM, PYGM, GBE1, ETFB, ETFA, ETFDH, GCDH, FXN, LRPPRC, FASTKD2, COX6B1, SLC3A1, ASS1, CYP27A1, SIX6, SLC22A5, SLC25A20, MGAT2, PMM2, PRKN, BBS7, BBS5, BBS12, MKS1, BBS9, BBS10, BBS4, BBS1, BBS2, APTX, ASL, TPP1, CLN3, ALMS1, HESX1, KIF21A, WWOX, SNCB, PNKD, SOD1, NEFH, GSN, TACO1, TMLHE, SLC6A8, MTFMT, SDHA, ABCD4, AGA, AHCY, ARSB, DOLK, DPAGT1, MOGS, HPD, TSHR, FGFR3, AR, ARSA, ASPA, ARX, ELP1, GBA, BRAF, CDKL5, CHD7, CREBBP, DHCR7, DMD, EIF2B1, FOXG1, GJC2, HRAS, IDS, IDUA, IKBKG, KRAS, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PORCN, PTPN11, RAI1, SHOC2, SLC2A1, SMN1, SOS1, WDR62, FGFR2, HDAC8, TSC2, RAD21, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, ATM, MRE11, NBN, PTCH1, PHOX2B, MET, GPC3, RAD50, CHRNE, CLN6, CLN8, DOK7, FKTN, NEB, PEX2, PROP1, PPT1, PEX7, SGCA, SGCB, SACS, TH, MLC1, PEX1, POMGNT1, SGCG, SLC12A6, SLC17A5, SUMF1, TTPA, ABCC8, CAPN3, CLN5, EIF2B5, PLA2G6, RAPSN, TMEM216, NDRG1, SBF2, PRX, FIG4, FGD4, SH3TC2, MTMR2, GDAP1, TRPV4, MPZ, PMP22, NEFL, HSPB8, LITAF, RAB7A, EGR2, HSPB1, YARS, DNM2, LMNA, GJB1, NTRK1, WNK1, SPTLC1, ATL1, ZFYVE26, EIF2B3, SMN2, EIF2B2, EIF2B4, SPG11, CSTB, SCN1A, PSEN2, MAPT, APOE, C9orf72, AHI1, NOTCH3, CLCN1, FKRP, CAV3, UBA1, CNBP, DYSF, SCN4A, ATXN3, CACNA1A, TOR1A, THAP1, GCH1, NF1, LRRK2, SGCE, SNCA, FGFR1, KCNJ11, CASR, INS, INF2, LAMB2, BSND, CLCNKB, KCNJ1, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, MATR3, SPAST, KIF5A, ATP2A1, L1CAM, NIPA1, SLC33A1, BSCL2, WASHC5, RTN2, BAG3, FHL1, SELENON, PNPLA6, KIF1A, CYP7B1, AP5Z1, FA2H, SPART, SPG21, ALS2, CACNA1S, RYR1, SIGMAR1, FUS, SETX, DCTN1, CHMP2B, TARDBP, ANG, VAPB, PFN1, UBQLN2, TPM3, ACTA1, CCDC78, KBTBD13, CNTN1, CFL2, TPM2, TNNT1, MTM1, BIN1, BICD2, DYNC1H1, HSPB3, VRK1, IGHMBP2, SYNE1, SYNE2, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, KCNA1, CACNB4, SLC1A3, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, SYT14, ANO10, TDP1, SIL1, GRM1, VAMP1, EEF2, KCND3, KCNC3, ITPR1, PDYN, FGF14, TGM6, TTBK2, SPTBN2, LAMA2, POMGNT2, COL6A2, COL6A3, LARGE1, COL6A1, MCPH1, ASPM, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, SYNJ1, SLC35A2, SLC6A1, FOLR1, GABRD, GRIN2B, KCNT1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, SCN5A, ALG13, ASAH1, TBC1D24, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, COL4A1, ARFGEF2, CENPJ, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, KRIT1, DNAJC5, MFSD8, ATP13A2, CCM2, PDCD10, KMT2D, RBFOX1, MAGI2, SETD2, TBL1XR1, SLC13A5, NEXMIF, SZT2, WDR45, ST3GAL3, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGN, PIGV, ANKRD11, PLCB1, SPTAN1, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, SERPINI1, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, VPS13A, TBX1, LBR, ATP2A2, HTRA1, SHANK3, SHANK2, ACTB, ACTG1, CACNA1D, EDN3, ERCC2, NLRP3, DNMT1, EDNRB, SOX10, PRPS1, CHSY1, GJB3, MYH14, MYH9, PEX6, TFAP2A, DIAPH3, ADNP, MID1, MED12, LAMC3, KIRREL3, FOXP2, FOXP1, EHMT1, CACNA1C, AP1S2, CHD8, HOXA1, TMEM231, ARID1B, CTNNB1, NLGN4X, NLGN3, PEX14, PEX19, PEX13, PEX3, PEX16, PEX26, PEX10, PEX12, PEX5, KAT6B, CLCNKA, MVK, FOXP3, NEU1, CHRNG, PHF8, IGBP1, HUWE1, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, FANCB, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, ZCCHC12, MSX2, TWIST1, NSUN2, CLCN2, NEDD4L, MTOR, VANGL1, EXOSC3, TSEN34, TSEN2, TGIF1, ZIC2, CEP152, CDON, GLI2, CDK5RAP2, FLVCR2, PCNT, ATR, NAGA, HYAL1, TGFB2, TGFBR1, TGFBR2, SKI, ACTA2, ABCC6, NFIX, RNF135, GLI3, TP63, MAGEL2, KDM6A, MARS, COX6A1, PLEKHG5, TRIM2, PDK3, SBF1, GNB4, DHTKD1, DNAJB2, HINT1, TFG, LRSAM1, AARS, MED25, GAN, IFT140, BLOC1S6, SLC4A4, ACVRL1, DOCK8, CSF2RB, NKX2-1, PRKAG2, AMPD1, COL12A1, LIMS2, MYF6, TNPO3, MTMR14, HNRNPDL, SLC5A7, POMK, GMPPB, LZTFL1, IFT27, BBIP1, WDPCP, SDCCAG8, PIEZO2, CHMP1A, ERCC6, KMT2A, SMARCA4, SMARCB1, ARID1A, SMARCA2, ERLIN1, REEP2, MAG, PGAP1, ENTPD1, NT5C2, KIF1C, C19orf12, UCHL1, B4GALNT1, TUBB4A, GBA2, CYP2U1, DDHD2, TECPR2, DDHD1, ADAR, VPS37A, ERLIN2, RAB3GAP2, AP4S1, AP4B1, AP4E1, AP4M1, ZFYVE27, KIF11, CTDP1, PGK1, FGF10, SLC9A9, LHX4, ACE, CD320, ALX4, EP300, RNASET2, EFTUD2, ASXL1, CCT5, GNPAT, CTC1, NOD2, FTL, CP, COASY, DCAF17, BDNF, MASP1, VEGFA, B9D1, ZIC3, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, EOMES, PIK3CA, RAB18, IER3IP1, RBBP8, MYCN, VLDLR, MARS2, COX10, SCO1, COG4, ALG11, COG6, COG5, TMEM165, IL11RA, CSF1R, TREM2, PRNP, SORL1, TPK1, SLC20A2, FBXO7, EARS2, DRD2, SLC6A3, PCBD1, APOA1, B9D2, ABCA1, PTF1A, VPS35, GP1BA, A2M, FGA, MYO5A, VIPAS39, CD36, VAX1, FREM1, ALX1, B3GLCT, PIK3R2, AKT3, AKT1, SLC4A1, RBM8A, NHEJ1, XK, LPIN2, FADD, DST, COL7A1, RANBP2, PRKRA, NOTCH2, TCTN3, UNC93B1, TRAF3, TICAM1, NLRP12, OCLN, NTRK2, PIGL, PDE6D, CSPP1, WNT5A, HEPACAM, RIN2, ZNF423, DYNC2H1, GRIP1, ESCO2, DHH, ROR2, WNT7A, ICK, ARSE, MAMLD1, PREPL, ASNS, SNAP29, CCDC88C, MPDZ, LAMB1, MED17, ZNF335, CEP135, KNL1, CEP63, TTI2, TAF2, NDST1, CRADD, EPB41L1, CACNG2, ANK3, TECR, MED23, LRP2, LINS1, C12orf57, SOBP, CDH15, TRAPPC9, PRSS12, MAN1B1, GRIK2, CRBN, CC2D1A, CA8, CD96, ALX3, ORC1, RNU4ATAC, AMPD2, SEPSECS, ASXL3, TUBGCP6, TSHB, TG, TBCE, DNAJC6, ANO3, HPCA, BCAP31, GNAL, ADCY5, SLC30A10, ACY1, AAAS, ATP8A2, ATP2B3, CAMTA1, ATCAY, COL18A1, GRID2, NOL3, PIK3R5, ELOVL5, ERCC5, NAT8L, STUB1, ITM2B, LMNB1, MAPK10, RUBCN, ZNF592, COA5, WDR81, POLR3A, POLR3B, RNF170, CHCHD10, CWF19L1, SCN10A, AP1S1, DSC3, KCNE5, WNT10A, EIF4G1, IL1RN, ARHGAP31, CERS1, ASCL1, GDNF, RETREG1, NGF, ARHGEF10, HOXD10, FAM126A, COL4A2, GYG1, PEX11B, POGZ, TRPS1, IFRD1, NOP56, UMPS, GLRB, TFAP2B, CST3, GLRA1, IGF1, SLC6A5, DRD3, TRPM6, NOS3, HDAC4, CIZ1, LYZ, PDE8B, HPSE2, PLEKHG4, EXOC8, AIMP1, IRX5, WNT3, TUBA4A, MSX1, TMCO1, GIGYF2, SNCAIP, ERCC1, ZBTB16, FTO, CHRM3, EXOSC8, TRPM7, FBXO38, YWHAE, CACNA1B, ALAD, KANK1, UPB1, NECTIN1, PRRX1, NOG, ATP2B4, ZFR, WDR48, USP8, ARSI, STRADA, RBFOX3, NDUFA4, ERBB4, WAC, HERC2, KCNK9, ADK, FLRT1, NXF5, ELK1, NRG1, VDAC1, DNAH9, FZD9, CD59, JRK, ACKR1, CD207, CR1, CNTNAP4, CDK11A, RABGGTA, TNFSF4, FRG1, TAS2R38, CISH, SNX3, ICAM1, YAP1, ADAM10, ZBTB18, EIF4E, SNIP1, AANAT, KCNK18, XBP1, NOS2, TIRAP, TLR5, PRKCH, ALOX5AP, TNF, FCGR2B
Specificity
1 %
Genes
67 %
|
GPR56.
By Amplexa Genetics Amplexa Genetics A/S in Denmark.
ADGRG1
Specificity
100 %
Genes
34 %
|
Neuronal Migration Disorders Panel.
By CeGaT GmbH in Germany.
TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1 , (...)
View the complete list with 30 more genes
TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1, ARFGEF2, DCX, EMX2, RAB3GAP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, MED12, LAMC3, FAT4, POMK, GMPPB, RAB3GAP2, EOMES, PIK3CA, RAB18, IER3IP1, VLDLR, PIK3R2, RTTN, TUBG1, KIF5C, KIF2A, SNAP29, DCHS1
Specificity
2 %
Genes
34 %
|
Neuronal Migration Disorders Panel.
By CeGaT GmbH in Germany.
TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1 , (...)
View the complete list with 30 more genes
TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1, ARFGEF2, DCX, EMX2, RAB3GAP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, TUBB2B, ACTB, ACTG1, MED12, LAMC3, FAT4, POMK, GMPPB, RAB3GAP2, EOMES, PIK3CA, RAB18, IER3IP1, VLDLR, PIK3R2, RTTN, TUBG1, KIF5C, KIF2A, SNAP29, DCHS1
Specificity
2 %
Genes
34 %
|
Ataxia and differential diagnoses Panel.
By CeGaT GmbH in Germany.
FMR1, AARS2, ABHD12, UQCRQ, BTD, ATP7B, AUH, TWNK, PRKCG, PAX6, INPP5E, AMACR, OPA1, WFS1, GLB1, CC2D2A, ELOVL4, TMEM67, NPHP1, CEP290 , (...)
View the complete list with 184 more genes
FMR1, AARS2, ABHD12, UQCRQ, BTD, ATP7B, AUH, TWNK, PRKCG, PAX6, INPP5E, AMACR, OPA1, WFS1, GLB1, CC2D2A, ELOVL4, TMEM67, NPHP1, CEP290, POLG, AFG3L2, OPA3, COQ9, PDSS2, PDSS1, ACO2, TTC19, MTPAP, NUBPL, SPR, COQ8A, DARS2, TSFM, DNAJC19, FLVCR1, PDP1, COQ2, SPG7, ALG6, ABCB7, HEXA, ALDH5A1, HEXB, PHYH, NDUFS7, NAGLU, DLAT, GALC, L2HGDH, GCDH, FXN, FASTKD2, CYP27A1, PMM2, APTX, TPP1, WWOX, PDHX, ARSA, GBA, EIF2B1, NPC1, NPC2, ATXN1, ATM, MRE11, CLN6, MTTP, PEX2, PEX7, SACS, SLC17A5, TTPA, CLN5, EIF2B5, PLA2G6, TMEM216, GJB1, EIF2B3, EIF2B2, EIF2B4, CSTB, AHI1, PPP2R2B, ATXN2, ATXN3, ATXN10, ATXN7, CACNA1A, TBP, ATN1, BSCL2, PNPLA6, SETX, VRK1, SYNE1, TRAPPC11, KCNA1, CACNB4, SLC1A3, SYT14, ANO10, TDP1, SIL1, GRM1, VAMP1, EEF2, KCND3, KCNC3, ITPR1, PDYN, FGF14, TGM6, TTBK2, SPTBN2, ATP1A3, GOSR2, NHLRC1, PRICKLE1, SLC19A3, SCN2A, SLC6A1, FOLR1, HCN1, KCNC1, EPM2A, LMNB2, PRRT2, RELN, TSEN54, ADGRG1, CTSF, DNAJC5, KCNA2, SNAP25, PNKP, KCNJ10, GFAP, ERCC2, ERCC3, POLR1C, DNMT1, PRPS1, PEX10, NEU1, CLCN2, NALCN, NKX2-1, GMPPB, ERCC6, KIF1C, UCHL1, GBA2, WNT1, CP, ERCC4, RPGRIP1L, ARL13B, VLDLR, MARS2, DNAJC3, CCDC88C, CA8, COX20, UBA5, RARS, ATP8A2, ATP2B3, CACNA1G, BEAN1, ATCAY, SLC52A2, LAMA1, GRID2, PIK3R5, PCNA, DMXL2, PTRH2, ELOVL5, RNASEH1, RNF216, SCYL1, ERCC5, STUB1, SLC9A1, RUBCN, PMPCA, TRNT1, XPA, WDR81, POLR3A, POLR3B, RNF170, CHCHD10, SNX14, TMEM240, WDR73, CWF19L1, VWA3B, XPC, NOP56, POLH, RPIA
Specificity
1 %
Genes
34 %
|
Test for Polymicrogyria.
By All Wales Genetics Laboratory Institute of Medical Genetics in United Kingdom.
ADGRG1
Specificity
100 %
Genes
34 %
|
Brain malformations.
By Asper Biogene Asper Biogene LLC in Estonia.
TUBB3, INPP5E, CC2D2A, ATP6V0A2, SRD5A3, TMEM67, NPHP1, CEP290, DLD, SLC25A19, MECP2, PDHB, TUBA1A, RARS2, PDP1, GCSH, GLDC, AMT, PDHA1, DLAT , (...)
View the complete list with 125 more genes
TUBB3, INPP5E, CC2D2A, ATP6V0A2, SRD5A3, TMEM67, NPHP1, CEP290, DLD, SLC25A19, MECP2, PDHB, TUBA1A, RARS2, PDP1, GCSH, GLDC, AMT, PDHA1, DLAT, ETFB, ETFA, ETFDH, MKS1, PDHX, ARX, CREBBP, DHCR7, WDR62, NBN, FKTN, PEX2, PEX1, POMGNT1, SLC12A6, TMEM216, AHI1, FKRP, WASHC5, DYNC1H1, VRK1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, MCPH1, ASPM, ARFGEF2, CENPJ, DCX, NDE1, PQBP1, RAB3GAP1, RELN, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, PNKP, TCF4, KIF1BP, OFD1, ATRX, OPHN1, CASK, CUL4B, ZEB2, ACTB, ACTG1, LAMC3, TMEM231, FAT4, PEX14, PEX19, PEX13, PEX3, PEX16, PEX26, PEX10, PEX12, PEX5, EXOSC3, TSEN34, TSEN2, TUBB2A, CEP152, CDK5RAP2, PCNT, ATR, GPSM2, POMK, GMPPB, PIEZO2, CHMP1A, TUBB4A, RAB3GAP2, AP4M1, KIF11, EFTUD2, B9D1, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, RAB18, IER3IP1, VLDLR, DHCR24, PIK3R2, AKT3, NHEJ1, TCTN3, OCLN, ZNF423, CCND2, TBC1D20, RTTN, TUBG1, TUBB, KIF5C, KIF2A, ERMARD, SNAP29, LAMB1, CEP135, KNL1, CEP63, AMPD2, SEPSECS, TUBGCP6, CLP1
Specificity
2 %
Genes
67 %
|
qChip.
By Quantitative Genomic Medicine Laboratories, SL in Spain.
FMR1, UBE3A, APC, PTEN, TP53, FOXL2, EYA1, COL2A1, OCA2, APP, WT1, PAX6, RB1, LEMD3, HNF1B, ELN, OCRL, PITX2, JAG1, NDP , (...)
View the complete list with 106 more genes
FMR1, UBE3A, APC, PTEN, TP53, FOXL2, EYA1, COL2A1, OCA2, APP, WT1, PAX6, RB1, LEMD3, HNF1B, ELN, OCRL, PITX2, JAG1, NDP, NPHP1, CEP290, SHH, MECP2, FBN1, RS1, OTC, HCCS, GK, TIMM8A, SOX2, LMX1B, ARX, BRAF, CDKL5, CHD7, DHCR7, KRAS, MAP2K1, PLP1, PTPN11, RAI1, RUNX2, SOS1, SRY, MAP2K2, TSC2, SMC1A, NIPBL, NSD1, PTCH1, NF2, BMPR1A, SMAD4, BTK, PMP22, SCN1A, MAPT, AHI1, NF1, NR0B1, SHOX, CASR, ANOS1, SLC12A3, BSND, CLCNKB, KCNJ1, SLC12A1, COL4A5, PKD1, DCX, EMX2, SIX3, RELN, PAFAH1B1, ADGRG1, OFD1, PAK3, ZEB2, SHANK3, SALL1, PAX3, GATA3, EHMT1, CLCNKA, SOX3, IL1RAPL1, TWIST1, SOX9, TGIF1, ZIC2, TGFBR1, TGFBR2, GLI3, SNRPN, MITF, TP63, NKX2-5, SH2D1A, NR5A1, LHX4, SALL4, TBX5, EP300, SATB2, VEGFA, ZIC3, GATA4, MYCN, DISP1, SIM1, MNX1, IRF6, MID2, LMNB1, HOXD13, STS, TRPS1, HDAC4, TBX3, FBXW11, TRAPPC10, CBFB, IGF2, SEM1
Specificity
1 %
Genes
34 %
|
Bilateral frontoparietal Polymicrogyria: GPR56 gene sequence analysis.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.
ADGRG1
Specificity
100 %
Genes
34 %
|
Epilepsy and Seizure Disorders: Sequencing Panel.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
MTHFR, UBE3A, ADSL, ADGRV1, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH5A1, ALDH7A1, NDUFA1, CYP27A1 , (...)
View the complete list with 90 more genes
MTHFR, UBE3A, ADSL, ADGRV1, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH5A1, ALDH7A1, NDUFA1, CYP27A1, TPP1, CLN3, ARX, CDKL5, FOXG1, MEF2C, PCDH19, SLC2A1, WDR62, TSC2, TSC1, CLN6, CLN8, PPT1, CLN5, CSTB, SCN1A, CACNA1A, KCNJ11, CASR, KCNA1, CACNB4, MCPH1, ASPM, ATP1A2, CHRNB2, CPA6, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, FOLR1, HCN1, KCNT1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, HCN4, MBD5, KCNMA1, SCARB2, TBC1D24, PRRT2, BCKDK, CENPJ, DCX, EMX2, NDE1, SIX3, RELN, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, DNAJC5, MFSD8, MAGI2, ST3GAL3, SCN8A, NRXN1, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, PHF6, ARHGEF9, SYN1, OPHN1, ATP6AP2, CASK, ZEB2
Specificity
2 %
Genes
67 %
|
Brain Malformations: Sequencing Panel.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
TUBB3, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, WDR62, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2 , (...)
View the complete list with 30 more genes
TUBB3, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, WDR62, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2, DCX, PQBP1, RAB3GAP1, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, KIF1BP, OPHN1, CASK, ACTB, ACTG1, LAMC3, EXOSC3, TSEN34, TSEN2, CHMP1A, RAB3GAP2, TMEM237, TMEM138, RPGRIP1L, KIF7, CEP41, EOMES, VLDLR, RTTN
Specificity
4 %
Genes
67 %
|
Neurology: Sequencing Panel.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
UBE3A, ADSL, TUBB3, CC2D2A, TMEM67, NPHP1, ADGRV1, CEP290, SHH, POLG, SLC25A19, MECP2, LIAS, GAMT, GATM, STXBP1, TUBA1A, RARS2, CTSD, SLC25A22 , (...)
View the complete list with 144 more genes
UBE3A, ADSL, TUBB3, CC2D2A, TMEM67, NPHP1, ADGRV1, CEP290, SHH, POLG, SLC25A19, MECP2, LIAS, GAMT, GATM, STXBP1, TUBA1A, RARS2, CTSD, SLC25A22, SLC9A6, ALDH7A1, MKS1, TPP1, CLN3, ARX, CDKL5, DHCR7, FOXG1, MEF2C, PCDH19, SLC2A1, WDR62, TSC2, TSC1, PTCH1, CLN6, CLN8, FKTN, PPT1, POMGNT1, CLN5, TMEM216, CSTB, SCN1A, AHI1, FKRP, FGF8, VRK1, POMT2, POMT1, CACNB4, LARGE1, MCPH1, ASPM, ATP1A2, CHRNB2, CPA6, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, FOLR1, GRIN2B, KCNT1, KCNQ2, KCNQ3, PNPO, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, TBC1D24, PRRT2, BCKDK, ARFGEF2, CENPJ, DCX, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, DNAJC5, MFSD8, MAGI2, ST3GAL3, SCN8A, NRXN1, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, KIF1BP, ATRX, ARHGEF9, SYN1, OPHN1, ATP6AP2, CASK, ZEB2, ACTB, ACTG1, LAMC3, EHMT1, EXOSC3, TSEN34, TSEN2, TGIF1, ZIC2, CEP152, NODAL, FOXH1, GLI2, CDK5RAP2, PCNT, ATR, CHMP1A, RAB3GAP2, TMEM237, TMEM138, RPGRIP1L, KIF7, CEP41, EOMES, RAB18, RBBP8, MYCN, VLDLR, DISP1, RTTN, ZNF335, CEP135, KNL1, CEP63, NIN, CDC6, CDT1, ORC6, ORC4, POC1A, MAPK10
Specificity
2 %
Genes
67 %
|
Brain Malformations: Deletion/Duplication Panel.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
TUBB3, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, WDR62, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2 , (...)
View the complete list with 30 more genes
TUBB3, CC2D2A, TMEM67, NPHP1, CEP290, TUBA1A, RARS2, MKS1, ARX, WDR62, FKTN, POMGNT1, TMEM216, AHI1, FKRP, VRK1, POMT2, POMT1, LARGE1, ARFGEF2, DCX, PQBP1, RAB3GAP1, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, KIF1BP, OPHN1, CASK, ACTB, ACTG1, LAMC3, EXOSC3, TSEN34, TSEN2, CHMP1A, RAB3GAP2, TMEM237, TMEM138, RPGRIP1L, KIF7, CEP41, EOMES, VLDLR, RTTN
Specificity
4 %
Genes
67 %
|
Epilepsy and Seizure Disorders: Deletion/Duplication Panel.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
MTHFR, UBE3A, ADSL, ADGRV1, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, NDUFA1, TPP1, CLN3 , (...)
View the complete list with 87 more genes
MTHFR, UBE3A, ADSL, ADGRV1, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, NDUFA1, TPP1, CLN3, ARX, CDKL5, FOXG1, MEF2C, PCDH19, SLC2A1, WDR62, TSC2, TSC1, CLN6, CLN8, PPT1, CLN5, CSTB, SCN1A, CACNA1A, KCNJ11, CASR, KCNA1, CACNB4, MCPH1, ASPM, ATP1A2, CHRNB2, CPA6, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, FOLR1, HCN1, KCNT1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, HCN4, MBD5, KCNMA1, SCARB2, TBC1D24, BCKDK, CENPJ, DCX, EMX2, NDE1, SIX3, RELN, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, DNAJC5, MFSD8, MAGI2, ST3GAL3, SCN8A, NRXN1, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, PHF6, ARHGEF9, SYN1, OPHN1, ATP6AP2, CASK, ZEB2
Specificity
2 %
Genes
67 %
|
Epilepsy NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, BCS1L, C12orf65, ADSL, PAX6, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2, GNE, HSD17B10, TMEM67 , (...)
View the complete list with 323 more genes
MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, BCS1L, C12orf65, ADSL, PAX6, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2, GNE, HSD17B10, TMEM67, NPHP1, ADGRV1, CEP290, SHH, DLD, POLG, NDUFS4, SLC25A19, PANK2, RAF1, FH, SMPD1, MECP2, COQ9, PDSS2, PDSS1, TMEM70, ABAT, DPM3, GAMT, GATM, STXBP1, COQ8A, RFT1, TUBA1A, RARS2, COG1, COG8, KCNV2, CTSD, SLC25A22, MPDU1, DPM1, COG7, ALG9, ATIC, ALG1, ALG8, ALG2, COQ2, ALG12, B4GALT1, GCSH, GLDC, AMT, SCO2, SLC35A1, ALG6, MPI, ALG3, PDHA1, SLC9A6, HEXA, SUOX, ALDH5A1, HEXB, SLC35C1, ALDH7A1, QDPR, CTSA, NDUFA2, COX15, NDUFS8, NDUFS7, NDUFS3, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, MOCS2, MOCS1, NDUFA1, NDUFS1, NDUFV1, GALC, ALDH4A1, SLC25A15, L2HGDH, ETFB, ETFA, ETFDH, GCDH, LRPPRC, MGAT2, PMM2, APTX, TPP1, CLN3, TACO1, SDHA, AGA, ARSB, DOLK, DPAGT1, MOGS, HPD, FGFR3, ARSA, ASPA, ARX, BRAF, CDKL5, EIF2B1, FOXG1, HRAS, IDS, IDUA, KRAS, MAP2K1, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PTPN11, RAI1, SHOC2, SLC2A1, SOS1, WDR62, MAP2K2, TSC2, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, PTCH1, GPC3, CLN6, CLN8, FKTN, PEX2, PPT1, PEX7, MLC1, MCOLN1, PEX1, POMGNT1, SLC17A5, SUMF1, ABCC8, CLN5, EIF2B5, PLA2G6, DPYD, TMEM216, EIF2B3, EIF2B2, EIF2B4, CSTB, SCN1A, AHI1, NOTCH3, FKRP, SCN4A, CACNA1A, NF1, KCNJ11, FGF8, CASR, CLCNKB, KCNJ1, VRK1, POMT2, POMT1, KCNA1, CACNB4, LAMA2, LARGE1, MCPH1, ASPM, ATP1A2, CACNA1H, CHRNB2, EFHC1, LGI1, GABRB3, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SCN1B, SCN2A, FOLR1, GABRD, GRIN2B, HCN1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, HCN4, MBD5, KCNMA1, SCARB2, SCN5A, TBC1D24, PRRT2, COL4A1, ARFGEF2, CENPJ, DCX, EMX2, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, MFSD8, KMT2D, MAGI2, SCN8A, NRXN1, GRIN1, PIGV, PLCB1, SPTAN1, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, KIF1BP, SERPINI1, OFD1, SMS, ATRX, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, VPS13A, TBX1, LBR, ATP2A2, PEX6, FUCA1, PEX14, PEX3, PEX26, PEX12, PEX5, KAT6B, CLCNKA, NEU1, SPRED1, CCL2, CLCN2, VANGL1, TSEN34, TSEN2, TGIF1, ZIC2, CEP152, ABCB1, NODAL, CDON, GLI2, CDK5RAP2, FLVCR2, PCNT, ATR, GNPTG, GLI3, SCN2B, SCN3B, SCN4B, PGK1, RPGRIP1L, ARL13B, SLC46A1, NHEJ1, LIG4, SNAP29, MED17, ACY1, COL18A1, MAPK10, BUB1B, SCN10A, GLRB, GLRA1, SLC6A5, GPHN, CELSR1, EFHC2
Specificity
1 %
Genes
67 %
|
Polymicrogyria NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
TUBB3, TUBA1A, TUBA8, ADGRG1, SRPX2, TUBB2B, KIF1BP
Specificity
29 %
Genes
67 %
|
ADGRG1.
By Fulgent Genetics Fulgent Genetics in United States.
ADGRG1
Specificity
100 %
Genes
34 %
|
Comprehensive Epilepsy NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, AUH, BCS1L, TWNK, C12orf65, ADSL, PAX6, AMACR, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2 , (...)
View the complete list with 427 more genes
MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, AUH, BCS1L, TWNK, C12orf65, ADSL, PAX6, AMACR, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2, GNE, HSD17B10, TMEM67, NPHP1, ADGRV1, CEP290, SHH, ME2, DLD, POLG, NDUFS4, SLC25A19, PANK2, RAF1, FH, SMPD1, MECP2, COQ9, PDSS2, PDSS1, LIAS, BOLA3, TMEM70, ABAT, SLC25A12, DPM3, GAMT, GATM, STXBP1, COQ8A, RFT1, TUBA1A, RARS2, COG1, COG8, KCNV2, CTSD, SLC25A22, MPDU1, DPM1, COG7, ALG9, ATIC, ALG1, ALG8, ALG2, GRN, COQ2, ALG12, B4GALT1, GLUD1, GCSH, GLDC, AMT, SCO2, SLC35A1, ALG6, MPI, ALG3, PDHA1, SLC9A6, HEXA, SUOX, ALDH5A1, HEXB, SLC35C1, ALDH7A1, QDPR, CTSA, NDUFA2, COX15, SURF1, NDUFS8, NDUFS7, NDUFS3, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, MOCS2, MOCS1, NDUFA1, NDUFS1, NDUFV1, GALC, ALDH4A1, SLC25A15, L2HGDH, ETFB, ETFA, ETFDH, GCDH, LRPPRC, MGAT2, PMM2, APTX, TPP1, CLN3, WWOX, TACO1, FARS2, SLC6A8, SDHA, AGA, ARSB, DOLK, DPAGT1, MOGS, HPD, FGFR3, ARSA, ASPA, ARX, BRAF, CDKL5, CHRNA7, DHCR7, EIF2B1, FOXG1, HRAS, IDS, IDUA, KRAS, MAP2K1, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PTPN11, RAI1, SHOC2, SLC2A1, SOS1, WDR62, MAP2K2, TSC2, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, PTCH1, GPC3, CLN6, CLN8, FKTN, PEX2, PPT1, PEX7, MLC1, MCOLN1, PEX1, POMGNT1, SLC17A5, SUMF1, ABCC8, CLN5, EIF2B5, PLA2G6, DPYD, TMEM216, EIF2B3, EIF2B2, EIF2B4, CSTB, SCN1A, AHI1, NOTCH3, FKRP, SCN4A, CACNA1A, NF1, KCNJ11, FGF8, CASR, CLCNKB, KCNJ1, DYNC1H1, VRK1, POMT2, POMT1, KCNA1, CACNB4, SLC1A3, LAMA2, DPM2, LARGE1, MCPH1, ASPM, ATP1A2, CACNA1H, CHRNB2, CPA6, EFHC1, CRH, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, KCNH2, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, STX1B, SLC35A2, SLC6A1, FOLR1, GABRB2, GABRD, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, KCNC1, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, HCN4, MBD5, KCNMA1, SCARB2, SCN5A, SLC4A10, ALG13, TBC1D24, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, COL4A1, ARFGEF2, CENPJ, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, CTSF, DNAJC5, MFSD8, ATP13A2, KMT2D, RBFOX1, CACNA2D2, MAGI2, HNRNPU, TBL1XR1, EEF1A2, KCNA2, DNM1, SIK1, SNAP25, PURA, KCNB1, SLC13A5, DOCK7, NR2F1, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGV, PLCB1, SPTAN1, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, KIF1BP, SERPINI1, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, VPS13A, TBX1, LBR, ATP2A2, PEX6, FUCA1, NTNG1, MED12, PEX14, PEX3, PEX26, PEX12, PEX5, KAT6B, CLCNKA, NEU1, UBE2A, CLCN4, SPRED1, CCL2, CLCN2, NEDD4L, MTOR, VANGL1, TSEN34, TSEN2, TUBB2A, TGIF1, ZIC2, CEP152, ABCB1, NODAL, CDON, GLI2, CDK5RAP2, FLVCR2, PCNT, ATR, GNPTG, GLI3, SCN2B, SCN3B, SCN4B, KDM6A, SMARCA2, ADAR, PGK1, RPGRIP1L, ARL13B, COX10, SLC46A1, AKT3, NHEJ1, LIG4, ASNS, SNAP29, CCDC88C, MED17, ANK3, C12orf57, KCNH5, ACY1, COL18A1, MAPK10, BUB1B, SCN10A, DHFR, GLRB, GLRA1, SLC6A5, HDAC4, SLC12A5, GPHN, SRGAP2, TNK2, HCN2, GABBR2, RYR3, FASN, PIK3AP1, ARHGEF15, CNTN2, KPNA7, RBFOX3, BRD2, VDAC1, UBR5, NIPA2, CELSR1, EFHC2, RANGAP1, KCNAB2, HNRNPH1
Specificity
1 %
Genes
67 %
|
Polymicrogyria Panel.
By Blueprint Genetics in Finland.
TUBB3, FH, TUBA1A, WDR62, NDE1, TUBA8, ADGRG1, SRPX2, TUBB2B, KIF1BP, LAMC3, NSDHL, TUBB2A, GPSM2, RAB18, AKT3, OCLN
Specificity
12 %
Genes
67 %
|
Neuronal Migration Disorder Panel.
By Blueprint Genetics in Finland.
TUBB3, ATP6V0A2, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, PHGDH, L1CAM, DYNC1H1, POMT1, ISPD, LAMA2, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1, ARFGEF2 , (...)
View the complete list with 38 more genes
TUBB3, ATP6V0A2, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, PHGDH, L1CAM, DYNC1H1, POMT1, ISPD, LAMA2, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1, ARFGEF2, DCX, EMX2, NDE1, RAB3GAP1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, KIF1BP, ACTB, ACTG1, MED12, LAMC3, FAT4, NSDHL, TUBB2A, FLVCR2, GPSM2, GMPPB, RAB3GAP2, KIF7, PIK3CA, RAB18, VLDLR, PIK3R2, AKT3, OCLN, RTTN, KATNB1, TUBG1, MPDZ, LAMB1, SEPSECS, COL4A2, YWHAE
Specificity
4 %
Genes
67 %
|
Bilateral frontoparietal polymicrogyria.
By Bioarray in Spain.
ADGRG1
Specificity
100 %
Genes
34 %
|
Rapid microarray (CGH and SNP).
By Allele Diagnostics Allele Diagnostics in United States.
FMR1, UBE3A, VHL, APC, PTEN, TP53, USH1C, ATP7A, FOXL2, HBB, EYA1, OCA2, WT1, PAX6, CHM, RB1, HNF1B, RET, ELN, OCRL , (...)
View the complete list with 153 more genes
FMR1, UBE3A, VHL, APC, PTEN, TP53, USH1C, ATP7A, FOXL2, HBB, EYA1, OCA2, WT1, PAX6, CHM, RB1, HNF1B, RET, ELN, OCRL, PITX2, JAG1, NDP, HPRT1, NPHP1, ADGRV1, SHH, MECP2, FBN1, SDHB, STXBP1, TUSC3, OTC, HCCS, GK, TIMM8A, AMER1, BCOR, SLC3A1, APTX, SOX2, LMX1B, AR, ARSA, CDKL5, CHD7, CREBBP, DMD, FOXG1, GJB6, MEF2C, PCDH19, PLP1, PORCN, RAI1, RPS19, RUNX2, SLC2A1, SRY, TSC2, SYNGAP1, TSC1, NIPBL, NSD1, PTCH1, NF2, STK11, SDHD, GPC3, BMPR1A, SMAD4, ENG, CTNS, CYBB, ABCC8, BTK, PMP22, SCN1A, GCH1, NF1, SGCE, NR0B1, SHOX, ANOS1, GHR, COL4A5, PKD1, MTM1, EMD, LARGE1, SCN2A, KCNQ2, MBD5, DCX, SIX3, PAFAH1B1, ADGRG1, KRIT1, CCM2, PDCD10, MAGI2, NRXN1, TCF4, CNTNAP2, FGD1, GRIA3, OPHN1, CASK, ZEB2, VPS13B, TBX1, SHANK2, SALL1, COL4A6, PAX3, EDNRB, SOX10, FGF3, GATA3, OTOA, MID1, FOXP2, FOXP1, EHMT1, PHF8, FTSJ1, SOX3, NSDHL, IL1RAPL1, MSX2, TWIST1, SOX9, TGIF1, ZIC2, GLI3, MITF, ACVRL1, DOCK8, NKX2-5, SH2D1A, NR5A1, KCNQ1OT1, LHX4, ALX4, SALL4, TBX5, EFNB1, F9, F8, ZIC3, MYCN, VLDLR, EXT2, XK, EDA, NFIA, MNX1, CCNQ, IRF6, ARSE, MAMLD1, PREPL, FLI1, GRIK2, STS, TRPS1, HDAC4, TBX3, YWHAE, FBXW4, IGF2, SEM1, CRK
Specificity
1 %
Genes
34 %
|
High-Resolution Rapid Microarray (CGH and SNP).
By Allele Diagnostics Allele Diagnostics in United States.
FMR1, UBE3A, VHL, APC, PTEN, TP53, USH1C, ATP7A, FOXL2, HBB, EYA1, OCA2, WT1, PAX6, CHM, RB1, HNF1B, RET, ELN, OCRL , (...)
View the complete list with 153 more genes
FMR1, UBE3A, VHL, APC, PTEN, TP53, USH1C, ATP7A, FOXL2, HBB, EYA1, OCA2, WT1, PAX6, CHM, RB1, HNF1B, RET, ELN, OCRL, PITX2, JAG1, NDP, HPRT1, NPHP1, ADGRV1, SHH, MECP2, FBN1, SDHB, STXBP1, TUSC3, OTC, HCCS, GK, TIMM8A, AMER1, BCOR, SLC3A1, APTX, SOX2, LMX1B, AR, ARSA, CDKL5, CHD7, CREBBP, DMD, FOXG1, GJB6, MEF2C, PCDH19, PLP1, PORCN, RAI1, RPS19, RUNX2, SLC2A1, SRY, TSC2, SYNGAP1, TSC1, NIPBL, NSD1, PTCH1, NF2, STK11, SDHD, GPC3, BMPR1A, SMAD4, ENG, CTNS, CYBB, ABCC8, BTK, PMP22, SCN1A, GCH1, NF1, SGCE, NR0B1, SHOX, ANOS1, GHR, COL4A5, PKD1, MTM1, EMD, LARGE1, SCN2A, KCNQ2, MBD5, DCX, SIX3, PAFAH1B1, ADGRG1, KRIT1, CCM2, PDCD10, MAGI2, NRXN1, TCF4, CNTNAP2, FGD1, GRIA3, OPHN1, CASK, ZEB2, VPS13B, TBX1, SHANK2, SALL1, COL4A6, PAX3, EDNRB, SOX10, FGF3, GATA3, OTOA, MID1, FOXP2, FOXP1, EHMT1, PHF8, FTSJ1, SOX3, NSDHL, IL1RAPL1, MSX2, TWIST1, SOX9, TGIF1, ZIC2, GLI3, MITF, ACVRL1, DOCK8, NKX2-5, SH2D1A, NR5A1, KCNQ1OT1, LHX4, ALX4, SALL4, TBX5, EFNB1, F9, F8, ZIC3, MYCN, VLDLR, EXT2, XK, EDA, NFIA, MNX1, CCNQ, IRF6, ARSE, MAMLD1, PREPL, FLI1, GRIK2, STS, TRPS1, HDAC4, TBX3, YWHAE, FBXW4, IGF2, SEM1, CRK
Specificity
1 %
Genes
34 %
|
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL.
By Laboratorio de Genetica Clinica SL in Spain.
ADGRG1
Specificity
100 %
Genes
34 %
|
Bilateral Frontoparietal Polymicrogyria , Sequencing GPR56 Gene.
By Reference Laboratory Genetics in Spain.
ADGRG1
Specificity
100 %
Genes
34 %
|
Polymicrogyria , Panel Massive Sequencing (NGS) 10 Genes.
By Reference Laboratory Genetics in Spain.
TUBB3, TUBA1A, FIG4, TUBA8, ADGRG1, SRPX2, TUBB2B, PIK3R2, AKT3, OCLN
Specificity
20 %
Genes
67 %
|
Malformations of Cortical Development , Panel Massive Sequencing (NGS) 38 Genes.
By Reference Laboratory Genetics in Spain.
TUBB3, TUBA1A, ARX, FOXG1, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, LARGE1, ASPM, COL4A1, ARFGEF2, DCX, NDE1, RELN, TUBA8 , (...)
View the complete list with 18 more genes
TUBB3, TUBA1A, ARX, FOXG1, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, LARGE1, ASPM, COL4A1, ARFGEF2, DCX, NDE1, RELN, TUBA8, FLNA, PAFAH1B1, ADGRG1, SRPX2, TUBB2B, KIF1BP, OPHN1, CASK, ACTB, ACTG1, LAMC3, GPSM2, PIK3CA, VLDLR, PIK3R2, AKT3, OCLN, LAMB1
Specificity
6 %
Genes
67 %
|
Polymicrogyria: gene sequencing.
By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.
ADGRG1
Specificity
100 %
Genes
34 %
|
Epilepsy Advanced Sequencing and CNV Evaluation - Intellectual Disability.
By Athena Diagnostics Inc in United States.
ADSL, HSD17B10, MECP2, ABAT, GAMT, GATM, ALG9, SLC9A6, SLC6A8, ARX, CDKL5, CHRNA7, PCDH19, PLP1, SMC1A, GPC3, DPYD, SLC35A2, FOLR1, GABRB2 , (...)
View the complete list with 36 more genes
ADSL, HSD17B10, MECP2, ABAT, GAMT, GATM, ALG9, SLC9A6, SLC6A8, ARX, CDKL5, CHRNA7, PCDH19, PLP1, SMC1A, GPC3, DPYD, SLC35A2, FOLR1, GABRB2, GRIN2B, ALG13, BCKDK, DEAF1, DCX, PQBP1, SRPX2, CACNA2D1, RBFOX1, HNRNPU, SETD2, SPATA5, EEF1A2, SNAP25, PURA, NEXMIF, WDR45, DYRK1A, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, GFAP
Specificity
2 %
Genes
34 %
|
NGS XLID Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, ARX , (...)
View the complete list with 94 more genes
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, ARX, CDKL5, DMD, IDS, PCDH19, PLP1, PORCN, HDAC8, SMC1A, GPC3, L1CAM, MTM1, DCX, PQBP1, FLNA, SRPX2, NEXMIF, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, OGT, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, ZC4H2, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, GSPT2, LAS1L, EIF2S3, FAAH2, WDR13, ZCCHC12, ZMYM3, FRMPD4, CLCN4, CCDC22, CDK16, CNKSR2, THOC2
Specificity
1 %
Genes
34 %
|
Non-Specific Intellectual Disability Panel.
By Genetic Services Laboratory University of Chicago in United States.
FMR1, UBE3A, HSD17B10, OCRL, HPRT1, NHS, MECP2, IDH2, STXBP1, TUBA1A, TUSC3, ALG6, D2HGDH, PDHA1, MAOA, ACSL4, SLC9A6, BCOR, ALDH5A1, L2HGDH , (...)
View the complete list with 153 more genes
FMR1, UBE3A, HSD17B10, OCRL, HPRT1, NHS, MECP2, IDH2, STXBP1, TUBA1A, TUSC3, ALG6, D2HGDH, PDHA1, MAOA, ACSL4, SLC9A6, BCOR, ALDH5A1, L2HGDH, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, PCDH19, PLP1, RAI1, SYNGAP1, SMC1A, L1CAM, KIF1A, DYNC1H1, SCN2A, GRIN2B, GRIN2A, MBD5, DEAF1, DCX, PQBP1, FLNA, SRPX2, PURA, NEXMIF, ST3GAL3, NRXN1, GRIN1, DYRK1A, KCNJ10, TCF4, CNTNAP2, OFD1, SMS, ATRX, IQSEC2, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, ZEB2, VPS13B, SHANK3, SHANK2, PRPS1, PTCHD1, ADNP, MID1, MED12, KIRREL3, FOXP1, EHMT1, AP1S2, ARID1B, CTNNB1, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MAGT1, ZNF711, ZNF41, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, ZDHHC9, BRWD3, CLIC2, SLC16A2, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, EIF2S3, FRMPD4, CCDC22, NSUN2, PCNT, DNMT3A, SOX11, SMARCA4, SMARCB1, ARID1A, PGAP1, DDHD2, ERLIN2, AP4S1, AP4B1, AP4E1, AP4M1, NRXN2, VLDLR, PACS1, KPTN, SLC25A1, ZMYND11, TTI2, TAF2, SLC6A17, SETD5, NDST1, MID2, METTL23, KIF4A, WASHC4, FMN2, FBXO31, EZR, CRADD, CLIP1, ADAT3, ZNF407, GATAD2B, EPB41L1, CTCF, CACNG2, ANK3, TECR, MED23, LRP2, LINS1, C12orf57, SOBP, CDH15, ZNF674, ZNF526, ZC3H14, TRAPPC9, PRSS12, MAN1B1, GRIK2, CRBN, CC2D1A, CA8
Specificity
1 %
Genes
34 %
|
X-linked Non-Specific Intellectual Disability Panel.
By Genetic Services Laboratory University of Chicago in United States.
FMR1, HSD17B10, OCRL, HPRT1, NHS, MECP2, PDHA1, MAOA, ACSL4, SLC9A6, BCOR, SLC6A8, ARX, CDKL5, PCDH19, PLP1, SMC1A, L1CAM, DCX, PQBP1 , (...)
View the complete list with 59 more genes
FMR1, HSD17B10, OCRL, HPRT1, NHS, MECP2, PDHA1, MAOA, ACSL4, SLC9A6, BCOR, SLC6A8, ARX, CDKL5, PCDH19, PLP1, SMC1A, L1CAM, DCX, PQBP1, FLNA, SRPX2, NEXMIF, OFD1, SMS, ATRX, IQSEC2, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MAGT1, ZNF711, ZNF41, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RPL10, ZDHHC9, BRWD3, CLIC2, SLC16A2, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, EIF2S3, FRMPD4, CCDC22, ZNF674
Specificity
2 %
Genes
34 %
|
Comprehensive Epilepsy Panel.
By GeneDx in United States.
UBE3A, ADSL, POLG, MECP2, LIAS, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, ARX, CDKL5, CHRNA7, FOXG1, MEF2C, PCDH19 , (...)
View the complete list with 50 more genes
UBE3A, ADSL, POLG, MECP2, LIAS, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, ARX, CDKL5, CHRNA7, FOXG1, MEF2C, PCDH19, SLC2A1, TSC2, TSC1, CLN6, CLN8, PPT1, CLN5, CSTB, SCN1A, CACNB4, ATP1A2, CHRNB2, EFHC1, LGI1, GOSR2, NHLRC1, KCTD7, PRICKLE1, SCN1B, SCN2A, FOLR1, GRIN2B, KCNQ2, KCNQ3, PNPO, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, SCARB2, TBC1D24, PRRT2, SRPX2, DNAJC5, MFSD8, MAGI2, KANSL1, SCN8A, NRXN1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, SYN1, ATP6AP2, ZEB2
Specificity
2 %
Genes
34 %
|
MECP2, SCN1B, GABRG2, LGI1, POLG, POLG2, SLC25A22, SPTAN1, SRPX2. NextGeneDx.Complete sequencing by NGS.
By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.
POLG, MECP2, POLG2, SLC25A22, LGI1, SCN1B, GABRG2, SRPX2, SPTAN1
Specificity
12 %
Genes
34 %
|
Rolandic Epilepsy - SRPX2 Sequence Analysis.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.
SRPX2
Specificity
100 %
Genes
34 %
|
Rolandic Epilepsy - SRPX2 Known Point Mutation Analysis.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.
SRPX2
Specificity
100 %
Genes
34 %
|
Rolandic epilepsy, mental retardation and speech dyspraxia (sequence analysis of SRPX2 gene).
By CGC Genetics in Portugal.
SRPX2
Specificity
100 %
Genes
34 %
|
Mental retardation, X-linked (NGS panel for 89 genes).
By CGC Genetics in Portugal.
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, SLC6A8 , (...)
View the complete list with 69 more genes
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, SLC6A8, ARX, CDKL5, DMD, IDS, PCDH19, PLP1, PORCN, HDAC8, SMC1A, GPC3, L1CAM, DCX, PQBP1, FLNA, SRPX2, NEXMIF, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, MID1, MED12, AP1S2, NLGN4X, PHF8, IGBP1, HUWE1, HCFC1, AFF2, MBTPS2, LAMP2, ZNF711, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, USP9X, GDI1, FTSJ1, RPS6KA3, SHROOM4, ZDHHC9, BRWD3, CLIC2, SLC16A2, SOX3, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, PGK1, MID2, KIF4A
Specificity
2 %
Genes
34 %
|
Comprehensive Epilepsy and Seizure Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics in United States.
UBE3A, ADSL, TUBB3, POLG, MECP2, GAMT, STXBP1, TUBA1A, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, WWOX, FARS2, ARX, CDKL5, FOXG1, MEF2C , (...)
View the complete list with 133 more genes
UBE3A, ADSL, TUBB3, POLG, MECP2, GAMT, STXBP1, TUBA1A, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, WWOX, FARS2, ARX, CDKL5, FOXG1, MEF2C, PCDH19, SLC2A1, TSC2, SYNGAP1, SMC1A, TSC1, CLN6, CLN8, PPT1, SLC17A5, CLN5, CSTB, SCN1A, CACNA1A, CACNB4, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, CRH, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, STX1B, SLC35A2, SLC6A1, FOLR1, GABRB2, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, KCNC1, PNPO, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, LMNB2, MBD5, KCNMA1, SCARB2, ALG13, TBC1D24, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, ARFGEF2, DCX, QARS, RELN, TUBA8, SRPX2, TUBB2B, CTSF, MFSD8, HNRNPU, SPATA5, EEF1A2, KCNA2, DNM1, SNAP25, PURA, KCNB1, SLC13A5, DOCK7, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGV, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, IQSEC2, ARHGEF9, SYN1, ATP6AP2, CASK, ZEB2, GFAP, NECAP1, CLCN2, NEDD4L, MTOR, TUBB2A, AARS, SMARCA2, IER3IP1, TUBG1, GNB1, ACY1, PIGG, SCN10A, NPRL3, NPRL2, TNK2, NACC1, CAD, FRRS1L, GRIN2D, HCN2, RORB, SON, PLPBP, SLC1A2, KCNH1, CARS2
Specificity
1 %
Genes
34 %
|
X-Linked Intellectual Disability Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics in United States.
FMR1, HSD17B10, NDP, HPRT1, NHS, MECP2, OTC, PDHA1, GK, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, TMLHE, SLC6A8, ARX, CDKL5, IDS , (...)
View the complete list with 108 more genes
FMR1, HSD17B10, NDP, HPRT1, NHS, MECP2, OTC, PDHA1, GK, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, TMLHE, SLC6A8, ARX, CDKL5, IDS, PCDH19, PLP1, HDAC8, SMC1A, GPC3, L1CAM, SLC35A2, ALG13, DCX, PQBP1, FLNA, SRPX2, NEXMIF, WDR45, PIGA, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, ZNF711, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, ZC4H2, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, IL1RAPL1, LAS1L, EIF2S3, FAAH2, ZCCHC12, ZMYM3, FRMPD4, CLCN4, CCDC22, CDK16, CNKSR2, THOC2, KDM6A, PGK1, HNRNPH2, BCORL1, ARSE, MID2, KIF4A, BCAP31, KCNE5, POLA1, DDX3X, SSR4, HMGB3, RNF113A, ARSF, H2BFWT, NONO, MSL3, DRP2, RLIM, MAGEA11, SLC7A3, MAP7D3, KLHL15, SYTL5, USP27X
Specificity
1 %
Genes
34 %
|
Epilepsy and Seizure Plus Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics in United States.
UBE3A, PTEN, ADSL, POLG, MECP2, LIAS, DHDDS, ABAT, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, GCSH, GLDC, AMT, SLC9A6, ALDH5A1, ALDH7A1 , (...)
View the complete list with 202 more genes
UBE3A, PTEN, ADSL, POLG, MECP2, LIAS, DHDDS, ABAT, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, GCSH, GLDC, AMT, SLC9A6, ALDH5A1, ALDH7A1, TPP1, CLN3, WWOX, PNKD, FARS2, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, PCDH19, SLC2A1, TSC2, CBL, SYNGAP1, SMC1A, TSC1, CLN6, CLN8, PPT1, SLC35A3, CLN5, CSTB, SCN1A, CACNA1A, NF1, SGCE, CASR, KCNA1, CACNB4, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, KCNH2, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, SYNJ1, STX1B, SLC35A2, SLC6A1, FOLR1, GABRB2, GABRD, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, KCNC1, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, LMNB2, MBD5, KCNMA1, SCARB2, SCN5A, ALG13, TBC1D24, PRIMA1, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, COL4A1, QARS, RELN, FLNA, SRPX2, DNAJC5, MFSD8, RBFOX1, CACNA2D2, HNRNPU, SETD2, TBL1XR1, SPATA5, EEF1A2, KCNA2, DNM1, SNAP25, PURA, KCNB1, SLC13A5, DOCK7, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGN, ANKRD11, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, SERPINI1, ATRX, IQSEC2, ARHGEF9, SYN1, ATP6AP2, CASK, ZEB2, DIAPH1, EHMT1, ARID1B, ZDHHC9, CLCN4, NECAP1, NEDD4L, MTOR, NAGA, DNMT3A, SATB2, IER3IP1, TPK1, RANBP2, PACS1, NTRK2, C12orf57, KCNH5, MDH2, UBA5, HIVEP2, ARV1, FGF12, COQ4, PRDM8, PIGG, CERS1, DDX3X, GLRA1, SLC12A5, GPHN, NGLY1, NPRL3, NPRL2, CAD, FRRS1L, GRIN2D, HCN2, RORB, PLPBP, KCNH1, CARS2, CLTC, GAL, GABBR2, GABRB1, PIGQ, PPP2R1A, PIGP, RYR3, KCND2, YWHAG, FASN, AP3B2, JMJD1C, PIK3AP1, PPP3CA, ARHGEF15, SNX27, CNTN2, ITPA, NUS1, RAB11A, STRADA, KPNA7, GUF1, HECW2, RBFOX3, DENND5A
Specificity
1 %
Genes
34 %
|
Mental Retardation and Dysmorphology - panels.
By MGZ Medical Genetics Center in Germany.
FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2 , (...)
View the complete list with 323 more genes
FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2, DHODH, PHKA2, PYGL, G6PC, IDH2, PHKG2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, PHKA1, ACSL4, SLC9A6, BCOR, HEXA, HEXB, PHKB, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, NDUFA1, MANBA, MAN2B1, CBS, PYGM, GBE1, SLC6A8, FGFR3, ASPA, ARX, GBA, BRAF, CDKL5, CHD7, CHRNA7, CREBBP, DHCR7, DMD, FOXG1, HRAS, IDS, IDUA, IKBKG, KRAS, MAP2K1, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PORCN, PTPN11, RAI1, SHOC2, SOS1, FGFR2, SOS2, HDAC8, RIT1, MAP2K2, TSC2, RAD21, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, PTCH1, CDKN1C, GPC3, PEX2, MLC1, MCOLN1, PEX1, SUMF1, EIF2B5, NF1, FGFR1, MYH7, L1CAM, WASHC5, FHL1, KIF1A, MTM1, EMD, GRIN2B, GRIN2A, MBD5, DCX, PQBP1, FLNA, SRPX2, KMT2D, SETD2, NEXMIF, WDR45, ST3GAL3, KANSL1, NRXN1, GRIN1, DYRK1A, ANKRD11, KCNJ10, TCF4, CNTNAP2, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, VPS13B, GFAP, SALL1, ACTB, ACTG1, EDN3, POLR1C, PAX3, EDNRA, EDNRB, SNAI2, SOX10, TCOF1, PRPS1, PEX6, TFAP2A, POLR1D, FUCA1, PTCHD1, MID1, MED12, FOXP2, FOXP1, EHMT1, AP1S2, CHD8, ARID1B, CTNNB1, NLGN4X, NLGN3, LZTR1, FAT4, PEX26, PEX10, PEX12, RASA1, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, LAS1L, EIF2S3, ZMYM3, CLCN4, CCDC22, THOC2, RAB23, POR, TWIST1, SPRED1, NSUN2, RASA2, RRAS, A2ML1, ABCC6, GNPTG, DNMT3A, NFIX, EZH2, RNF135, GLI3, ABCC9, GPSM2, MITF, TP63, MAGEL2, KDM6A, PITX1, ERCC6, SMARCE1, KMT2A, SMARCA4, SMARCB1, ARID1A, SMARCA2, PGK1, ALX4, SALL4, TBX5, EP300, EFNB1, EFTUD2, CTC1, TRIM37, GNAS, KIF7, CPLANE1, PIK3CA, GNAQ, ALX1, IDH1, INSR, PIK3R2, AKT3, AKT1, ERCC8, EPG5, PACS1, NOTCH2, TCTN3, C2CD3, UBR1, SRCAP, WNT5A, KPTN, TBC1D7, HEPACAM, CCND2, ROR2, CCNQ, IRF6, SPECC1L, CUL7, GATAD2B, EPB41L1, CTCF, CACNG2, ANK3, TECR, MED23, C12orf57, CDH15, ZNF674, TRAPPC9, GRIK2, CRBN, CC2D1A, ALX3, OBSL1, CCDC8, SNX14, SF3B4, HOXD13, ARHGAP31, FLNB, DDX3X, KAT6A, TRPS1, DOCK6, RBPJ, TBX3, DIS3L2, EOGT, DVL1, DCHS1, NOG, LMBR1, TXNL4A, DLL4, BCL11A, MED13L, STRADA, WAC, HERC2, NXF5, REV3L, PLXND1, NFATC2IP
Specificity
1 %
Genes
34 %
|
Syndromal Diseases - panels.
By MGZ Medical Genetics Center in Germany.
FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2 , (...)
View the complete list with 322 more genes
FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2, DHODH, PHKA2, PYGL, G6PC, IDH2, PHKG2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, PHKA1, ACSL4, SLC9A6, BCOR, HEXA, HEXB, PHKB, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, NDUFA1, MANBA, MAN2B1, CBS, PYGM, GBE1, SLC6A8, FGFR3, ASPA, ARX, GBA, BRAF, CDKL5, CHD7, CHRNA7, CREBBP, DHCR7, DMD, FOXG1, HRAS, IDS, IDUA, IKBKG, KRAS, MAP2K1, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PORCN, PTPN11, RAI1, SHOC2, SOS1, FGFR2, SOS2, HDAC8, RIT1, MAP2K2, TSC2, RAD21, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, PTCH1, CDKN1C, GPC3, PEX2, MLC1, MCOLN1, PEX1, SUMF1, EIF2B5, NF1, FGFR1, MYH7, L1CAM, WASHC5, FHL1, KIF1A, MTM1, EMD, GRIN2B, GRIN2A, MBD5, DCX, PQBP1, FLNA, SRPX2, KMT2D, SETD2, NEXMIF, WDR45, ST3GAL3, KANSL1, NRXN1, GRIN1, DYRK1A, ANKRD11, KCNJ10, TCF4, CNTNAP2, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, VPS13B, GFAP, SALL1, ACTB, ACTG1, EDN3, POLR1C, PAX3, EDNRA, EDNRB, SNAI2, SOX10, TCOF1, PRPS1, PEX6, TFAP2A, POLR1D, FUCA1, PTCHD1, MID1, MED12, FOXP2, FOXP1, EHMT1, AP1S2, CHD8, ARID1B, CTNNB1, NLGN4X, NLGN3, LZTR1, FAT4, PEX26, PEX10, PEX12, RASA1, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, LAS1L, EIF2S3, ZMYM3, CLCN4, CCDC22, THOC2, RAB23, POR, TWIST1, SPRED1, NSUN2, RASA2, RRAS, A2ML1, ABCC6, GNPTG, DNMT3A, NFIX, EZH2, RNF135, GLI3, ABCC9, GPSM2, MITF, TP63, MAGEL2, KDM6A, PITX1, ERCC6, SMARCE1, KMT2A, SMARCA4, SMARCB1, ARID1A, SMARCA2, PGK1, ALX4, SALL4, TBX5, EP300, EFNB1, EFTUD2, TRIM37, GNAS, KIF7, CPLANE1, PIK3CA, GNAQ, ALX1, IDH1, INSR, PIK3R2, AKT3, AKT1, ERCC8, EPG5, PACS1, NOTCH2, TCTN3, C2CD3, UBR1, SRCAP, WNT5A, KPTN, TBC1D7, HEPACAM, CCND2, ROR2, CCNQ, IRF6, SPECC1L, CUL7, GATAD2B, EPB41L1, CTCF, CACNG2, ANK3, TECR, MED23, C12orf57, CDH15, ZNF674, TRAPPC9, GRIK2, CRBN, CC2D1A, ALX3, OBSL1, CCDC8, SNX14, SF3B4, HOXD13, ARHGAP31, FLNB, DDX3X, KAT6A, TRPS1, DOCK6, RBPJ, TBX3, DIS3L2, EOGT, DVL1, DCHS1, NOG, LMBR1, TXNL4A, DLL4, BCL11A, MED13L, STRADA, WAC, HERC2, NXF5, REV3L, PLXND1, NFATC2IP
Specificity
1 %
Genes
34 %
|
X-Linked Mental Retardation.
By MGZ Medical Genetics Center in Germany.
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, NDUFA1, SLC6A8 , (...)
View the complete list with 93 more genes
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, NDUFA1, SLC6A8, ARX, CDKL5, DMD, IDS, IKBKG, PCDH19, PLP1, PORCN, HDAC8, SMC1A, GPC3, SLC12A6, L1CAM, FHL1, MTM1, EMD, DCX, PQBP1, FLNA, SRPX2, NEXMIF, WDR45, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, LAS1L, EIF2S3, ZMYM3, CLCN4, THOC2, KDM6A, GAN, CTDP1, PGK1, ZNF674, FAM126A, NXF5
Specificity
1 %
Genes
34 %
|
SRPX2.
By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.
SRPX2
Specificity
100 %
Genes
34 %
|
Epileptic syndromes with epilepsy and intellectual disability panel.
By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.
UBE3A, HSD17B10, MECP2, STXBP1, SLC9A6, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, PLP1, SYNGAP1, SMC1A, GPC3, GRIN2B, GRIN2A, MBD5, TBC1D24, DCX, PQBP1 , (...)
View the complete list with 30 more genes
UBE3A, HSD17B10, MECP2, STXBP1, SLC9A6, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, PLP1, SYNGAP1, SMC1A, GPC3, GRIN2B, GRIN2A, MBD5, TBC1D24, DCX, PQBP1, SRPX2, NRXN1, DYRK1A, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, OFD1, SMS, ATRX, FGD1, PHF6, SYP, GRIA3, PAK3, KDM5C, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, ZEB2, TREX1, MED12, CNKSR2, AUTS2
Specificity
2 %
Genes
34 %
|
Focal epilepsy panel.
By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.
CHRNB2, LGI1, KCNT1, CHRNA2, CHRNA4, GRIN2A, SRPX2, SYN1, ELP4
Specificity
12 %
Genes
34 %
|
Rolandic epilepsy, mental retardation, and speech dyspraxia.
By Centogene AG - the Rare Disease Company in Germany.
SRPX2
Specificity
100 %
Genes
34 %
|
Single gene testing SRPX2.
By CeGaT GmbH in Germany.
SRPX2
Specificity
100 %
Genes
34 %
|
Epilepsy.
By Asper Biogene Asper Biogene LLC in Estonia.
UBE3A, MCCC1, ADSL, TUBB3, POLG, MECP2, GAMT, GATM, STXBP1, SLC25A22, ALG3, SLC9A6, ALDH7A1, MOCS2, MOCS1, WWOX, SLC6A8, ARX, CDKL5, FOXG1 , (...)
View the complete list with 104 more genes
UBE3A, MCCC1, ADSL, TUBB3, POLG, MECP2, GAMT, GATM, STXBP1, SLC25A22, ALG3, SLC9A6, ALDH7A1, MOCS2, MOCS1, WWOX, SLC6A8, ARX, CDKL5, FOXG1, MEF2C, PCDH19, TSC2, SYNGAP1, TSC1, SLC35A3, CSTB, SCN1A, CACNA1A, KIF1A, DYNC1H1, KCNA1, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, ST3GAL5, SCN1B, SCN2A, STX1B, SLC35A2, SLC6A1, GABRD, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, KCNC1, PNPO, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, ALG13, TBC1D24, DEPDC5, PRRT2, BRAT1, PIGO, DCX, RELN, FLNA, SRPX2, SPATA5, EEF1A2, KCNA2, DNM1, SIK1, PURA, KCNB1, SLC13A5, DOCK7, NEXMIF, SZT2, GNAO1, WDR45, ST3GAL3, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, PLCB1, SPTAN1, PNKP, TCF4, SERPINI1, ATRX, IQSEC2, SYP, ARHGEF9, SYN1, ATP6AP2, CASK, CACNA1D, HUWE1, ZDHHC9, NECAP1, MTOR, AARS, SMARCA2, ADAR, KIF5C, FGF12, CERS1, SLC12A5, PIGT, GPHN, ITPA, SNIP1
Specificity
1 %
Genes
34 %
|
EPILEPSY HEREDITARY PANEL.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.
STXBP1, ALDH7A1, ARX, CDKL5, PCDH19, SLC2A1, MT-ATP6, SCN1A, CACNA1A, KCNA1, CACNB4, ATP1A2, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, NHLRC1, SCN9A , (...)
View the complete list with 17 more genes
STXBP1, ALDH7A1, ARX, CDKL5, PCDH19, SLC2A1, MT-ATP6, SCN1A, CACNA1A, KCNA1, CACNB4, ATP1A2, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, NHLRC1, SCN9A, SCN1B, SCN2A, GABRD, KCNQ2, KCNQ3, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, KCNMA1, DEPDC5, PRRT2, SRPX2, SCN8A, CLCN2, JRK
Specificity
3 %
Genes
34 %
|
Epileptic encephalopathies.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.
MECP2, STXBP1, SLC25A22, GCSH, GLDC, AMT, WWOX, ARX, CDKL5, PCDH19, SLC2A1, SCN1A, SCN2A, GRIN2B, HCN1, KCNQ2, CHD2, GABRA1, GRIN2A, MBD5 , (...)
View the complete list with 15 more genes
MECP2, STXBP1, SLC25A22, GCSH, GLDC, AMT, WWOX, ARX, CDKL5, PCDH19, SLC2A1, SCN1A, SCN2A, GRIN2B, HCN1, KCNQ2, CHD2, GABRA1, GRIN2A, MBD5, TBC1D24, DCX, SRPX2, DNM1, ST3GAL3, SCN8A, PIGA, PLCB1, SPTAN1, PNKP, ARHGEF9, CASK, TREX1, AARS, MAPK10
Specificity
3 %
Genes
34 %
|
XLMR with Rolandic Epilepsy and Speech Dyspraxia: SRPX2 Full Gene Sequencing.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
SRPX2
Specificity
100 %
Genes
34 %
|
XLMR with Rolandic Epilepsy and Speech Dyspraxia: SRPX2 Gene Deletion/Duplication.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
SRPX2
Specificity
100 %
Genes
34 %
|
Intellectual Disability NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
BRCA2, F5, FMR1, MTHFR, TTR, UBE3A, PTEN, MCCC1, MCCC2, AGL, ACAT1, GYS2, ARG1, ATP7A, AUH, BCS1L, ADSL, FBLN5, LRP5, COL1A2 , (...)
View the complete list with 372 more genes
BRCA2, F5, FMR1, MTHFR, TTR, UBE3A, PTEN, MCCC1, MCCC2, AGL, ACAT1, GYS2, ARG1, ATP7A, AUH, BCS1L, ADSL, FBLN5, LRP5, COL1A2, PAX6, TUBB3, MTR, CPS1, PYCR1, GNPTAB, CC2D2A, SRD5A3, HSD17B10, ELOVL4, NDP, TMEM67, NPHP3, MKKS, CEP290, HSPD1, GCK, SLC25A13, MECP2, FBN1, PDSS1, ALDH18A1, TMEM70, PHKA2, XPNPEP3, PYGL, PHKG2, SLC25A12, GAMT, SPR, STXBP1, TUBA1A, DARS2, TUSC3, HAX1, GFM1, COG7, AP3B1, ALG12, ALG6, MPI, MYO7A, STRA6, D2HGDH, AIFM1, ACSL4, AMER1, SLC9A6, ABCD1, MMADHC, LMBRD1, GM2A, HEXB, SLC35C1, ACOX1, PAH, CTSA, GUSB, SGSH, MOCS2, NDUFA1, NDUFS1, NDUFAF5, CYB5R3, DBT, MANBA, MAN2B1, SUCLG1, ALDH4A1, SLC25A15, CBS, GBE1, GALE, GLYCTK, ASS1, CYP27A1, MGAT2, BBS9, SOX2, CLN3, PPOX, KIF21A, SLC6A8, MTFMT, PDHX, HPD, TSHR, FGFR3, AR, ARX, GBA, CDKL5, CHD7, DHCR7, DMD, FOXG1, IDS, KRAS, MEF2C, NPC1, NPC2, PCDH19, PLP1, PTPN11, RAI1, SLC2A1, TINF2, WDR62, FGFR2, HDAC8, TSC2, SYNGAP1, SMC1A, TSC1, NIPBL, ATM, NBN, CDKN1C, BRIP1, PRKAR1A, FKTN, PEX7, SGCA, SLC7A7, SACS, TH, MCOLN1, POMGNT1, PLA2G6, RAPSN, DPYD, TMEM216, MPZ, SPTLC1, ATL1, ZFYVE26, SCN1A, MAPT, AHI1, FKRP, NF1, FGFR1, KCNJ11, POU1F1, GHR, AVPR2, KIF5A, L1CAM, KIF1A, BIN1, DYNC1H1, POMT2, POMT1, SYT14, SIL1, GRM1, FGF14, LAMA2, LARGE1, ITGA7, MCPH1, ASPM, ATP1A2, CPA6, KCTD7, PRICKLE1, GRIN2B, KCNQ2, CHRNA4, GABRG2, GRIN2A, MBD5, TBC1D24, PIGO, PQBP1, TUBA8, PAFAH1B1, SRPX2, TUBB2B, MFSD8, ATP13A2, ST3GAL3, SCN8A, NRXN1, GRIN1, DYRK1A, PIGV, SPTAN1, SAMHD1, KCNJ10, CNTNAP2, OFD1, SMS, ATRX, IQSEC2, FGD1, SYP, GRIA3, PAK3, KDM5C, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, ZEB2, VPS13B, GFAP, TBX1, LBR, SHANK3, SHANK2, ERCC2, ERCC3, SOX10, KIRREL3, FOXP1, EHMT1, AP1S2, ARID1B, CTNNB1, NLGN3, CANT1, PHF8, IGBP1, HUWE1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RAB40AL, ZDHHC9, BRWD3, SLC16A2, SOX3, NSDHL, ARHGEF6, IL1RAPL1, TWIST1, NSUN2, TGIF1, ZIC2, PCNT, NAGA, FBN2, ABCC6, GNPTG, GLI3, GAN, LYST, SLC4A4, SDCCAG8, ERCC6, SMARCA4, SMARCB1, ARID1A, ADAR, AP4S1, AP4B1, AP4E1, AP4M1, KIF11, PGK1, LHX3, THRB, ALX4, EFNB1, GNPAT, CTC1, NHP2, GNAS, FANCG, ABCG5, SLX4, CP, SATB2, SLC6A4, RPGRIP1L, KIF7, CEP41, RBBP8, MYCN, VLDLR, ALG11, COG5, TMEM165, SLC46A1, TPK1, SLC20A2, MAT1A, APOB, SLC2A2, RFX6, DHCR24, MYO5A, INSR, ERCC8, STX11, G6PC3, NHEJ1, LIG4, STAT5B, GSS, TTC37, PIGL, HEPACAM, ZFP57, PDE4D, CCDC88C, MED17, CRADD, CACNG2, TECR, MED23, SOBP, CDH15, TRAPPC9, PRSS12, MAN1B1, GRIK2, CRBN, CC2D1A, ORC1, WRN, SLC5A5, TBCE, ACY1, CAMTA1, ERCC5, UROC1, WDR81, BUB1B, AP1S1, AVP, NGF, HOXD10, FAM126A, TRHR, SLC5A2, GLRA1, IGF1, HDAC4, MRAP, IGF1R, AGT, IRX5, TMCO1, ZBTB16, FTO, CEP57, UPB1, KCNK9, DIP2B, GLUL, ZBTB24, SNIP1, XIST, AFP, TPH2, AQP7
Specificity
1 %
Genes
34 %
|
XLID NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1 , (...)
View the complete list with 87 more genes
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, AIFM1, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, ARX, CDKL5, DMD, IDS, PCDH19, PLP1, PORCN, HDAC8, SMC1A, GPC3, L1CAM, MTM1, DCX, PQBP1, FLNA, SRPX2, NEXMIF, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, GSPT2, FAAH2, WDR13, ZCCHC12, FRMPD4, CCDC22, CNKSR2, PGK1, ZNF674
Specificity
1 %
Genes
34 %
|
SRPX2.
By Fulgent Genetics Fulgent Genetics in United States.
SRPX2
Specificity
100 %
Genes
34 %
|
Idiopathic Generalized Epilepsy NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
UBE3A, ADSL, HSD17B10, ME2, MECP2, STXBP1, SLC9A6, ALDH7A1, ARX, CDKL5, FOXG1, MEF2C, PCDH19, PLP1, SLC2A1, SYNGAP1, SMC1A, GPC3, CSTB, SCN1A , (...)
View the complete list with 69 more genes
UBE3A, ADSL, HSD17B10, ME2, MECP2, STXBP1, SLC9A6, ALDH7A1, ARX, CDKL5, FOXG1, MEF2C, PCDH19, PLP1, SLC2A1, SYNGAP1, SMC1A, GPC3, CSTB, SCN1A, CACNA1A, CASR, DYNC1H1, CACNB4, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SCN1B, SCN2A, STX1B, GABRD, KCNT1, KCNQ2, KCNQ3, KCNC1, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, TBC1D24, DEPDC5, PRRT2, DCX, PQBP1, SRPX2, DNAJC5, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, KCNJ10, TCF4, CNTNAP2, OFD1, ATRX, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, ZEB2, CLCN2, DHFR, CNTN2, NIPA2
Specificity
2 %
Genes
34 %
|
Early-Onset Epileptic Encephalopathy NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
UBE3A, AUH, ADSL, ADGRV1, POLG, MECP2, LIAS, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, WWOX, FARS2, SLC6A8 , (...)
View the complete list with 113 more genes
UBE3A, AUH, ADSL, ADGRV1, POLG, MECP2, LIAS, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, WWOX, FARS2, SLC6A8, ARX, CDKL5, CHRNA7, FOXG1, MEF2C, PCDH19, SLC2A1, TSC2, SYNGAP1, TSC1, CLN6, CLN8, PPT1, CLN5, CSTB, SCN1A, CACNA1A, DYNC1H1, CACNB4, ATP1A2, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, KCNH2, PRICKLE1, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, STX1B, SLC35A2, FOLR1, GABRB2, GABRD, GRIN2B, HCN1, KCNT1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, SCARB2, SCN5A, ALG13, TBC1D24, DEPDC5, PRRT2, PIGO, BCKDK, ARFGEF2, QARS, SRPX2, CTSF, DNAJC5, MFSD8, RBFOX1, CACNA2D2, MAGI2, HNRNPU, EEF1A2, DNM1, SIK1, KCNB1, SLC13A5, NR2F1, SZT2, GNAO1, WDR45, ST3GAL3, KANSL1, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGV, PLCB1, SPTAN1, PNKP, KCNJ10, TCF4, CNTNAP2, IQSEC2, ARHGEF9, SYN1, ATP6AP2, ZEB2, CLCN4, NEDD4L, MTOR, KCNH5, ACY1, SLC12A5, TNK2, HCN2, ARHGEF15, KPNA7, RBFOX3
Specificity
1 %
Genes
34 %
|
X-chromosome High Resolution microarray analysis.
By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.
ATP7A, OPN1MW, CHM, GPR143, HSD17B10, OCRL, CACNA1F, NDP, HPRT1, NHS, ALAS2, RPGR, MECP2, RS1, PHKA2, RP2, OTC, HCCS, PDHA1, GK , (...)
View the complete list with 140 more genes
ATP7A, OPN1MW, CHM, GPR143, HSD17B10, OCRL, CACNA1F, NDP, HPRT1, NHS, ALAS2, RPGR, MECP2, RS1, PHKA2, RP2, OTC, HCCS, PDHA1, GK, TIMM8A, TAZ, ABCB7, AIFM1, MAOA, PHKA1, ACSL4, AMER1, SLC9A6, BCOR, ABCD1, TMLHE, SLC6A8, IL2RG, AR, ARX, CDKL5, DMD, GLA, IDS, IKBKG, PCDH19, PLP1, PORCN, POU3F4, SRY, HDAC8, G6PD, CYBB, WAS, BTK, GJB1, UBA1, NR0B1, SHOX, ANOS1, AVPR2, COL4A5, L1CAM, FHL1, UBQLN2, MTM1, EMD, SLC35A2, ALG13, DCX, PQBP1, FLNA, SRPX2, WDR45, PIGA, OFD1, SMS, ATRX, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, RAB39B, PRPS1, SMPX, MID1, MED12, AP1S2, NLGN4X, NLGN3, GATA1, PHF8, IGBP1, HCFC1, AGTR2, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, ZC4H2, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KDM6A, CSF2RA, PGK1, SH2D1A, EFNB1, F9, F8, ZIC3, XIAP, XK, EDA, CCNQ, ARSE, MAMLD1, ZNF674, IGSF1, CLCN5, ATP2B3, STS, POLA1, CFP, AMELX, TRAPPC2, VMA21, CHRDL1, COX7B, TBX22, SLC6A14, SAT1, SERPINA7
Specificity
1 %
Genes
34 %
|
X-linked Intellectual Disability Panel.
By Blueprint Genetics in Finland.
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, SLC6A8 , (...)
View the complete list with 79 more genes
FMR1, ATP7A, HSD17B10, OCRL, NDP, HPRT1, NHS, MECP2, OTC, HCCS, PDHA1, GK, TIMM8A, MAOA, ACSL4, SLC9A6, BCOR, ABCD1, NDUFA1, SLC6A8, ARX, CDKL5, IDS, PCDH19, PLP1, PORCN, SMC1A, GPC3, L1CAM, MTM1, DCX, PQBP1, FLNA, SRPX2, NEXMIF, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, PRPS1, PTCHD1, MID1, MED12, AP1S2, NLGN4X, NLGN3, PHF8, IGBP1, HUWE1, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, ZNF41, FANCB, DKC1, DLG3, TSPAN7, UBE2A, UPF3B, USP9X, ZC4H2, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, ZDHHC9, BRWD3, TAF1, SLC16A2, SOX3, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, ZCCHC12, CLCN4, PGK1, ZNF674, DDX3X, NXF5, ELK1
Specificity
2 %
Genes
34 %
|
Familial Epilepsy and Related Disorders , Panel Massive Sequencing (NGS) 34 Genes.
By Reference Laboratory Genetics in Spain.
STXBP1, ALDH7A1, ARX, CDKL5, PCDH19, SLC2A1, SCN1A, CACNA1A, KCNA1, CACNB4, ATP1A2, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, NHLRC1, SCN9A, SCN1B , (...)
View the complete list with 14 more genes
STXBP1, ALDH7A1, ARX, CDKL5, PCDH19, SLC2A1, SCN1A, CACNA1A, KCNA1, CACNB4, ATP1A2, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, NHLRC1, SCN9A, SCN1B, SCN2A, GABRD, KCNQ2, KCNQ3, CHRNA2, CHRNA4, EPM2A, GABRA1, GABRG2, KCNMA1, PRRT2, SRPX2, SCN8A, CLCN2
Specificity
3 %
Genes
34 %
|