Osteogenesis Imperfecta, Type Iii; Oi3

Description

Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI; see this term), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. The main signs of type III include very short stature, a triangular face, severe scoliosis, grayish sclera, and dentinogenesis imperfecta (DI; see this term).

Genes related to Osteogenesis Imperfecta, Type Iii; Oi3

FKBP10
COL1A1
COL1A2
BMP1
CREB3L1
PPIB
P3H1
CRTAP
SERPINH1
WNT1
SERPINF1

Clinical Features

Top most frequent phenotypes and symptoms related to Osteogenesis Imperfecta, Type Iii; Oi3

Hearing impairment
Scoliosis
Micrognathia
Frontal bossing
Kyphosis
Kyphoscoliosis
Abnormality of the nervous system
Triangular face
Recurrent fractures
Blue sclerae

And another 16 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Not enough data available about incidence and published cases.

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Osteogenesis Imperfecta, Type Iii; Oi3 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
FKBP10 Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. FKBP10 Specificity 100 % Genes 10 %
MitoMet®Plus aCGH Analysis. By Baylor Miraca Genetics Laboratories in United States. GSN, NEFH, SOD1, TEAD1, PHB, PLA2G2A, AKAP10, PNKD, PAX2, CPOX, ABCB7, TAZ, TIMM8A, GK, PDHA1, HCCS, NYX, FRMD7, OTC, RP2 , (...) View the complete list with 617 more genes Panel GTR000508280 complete gene list GSN, NEFH, SOD1, TEAD1, PHB, PLA2G2A, AKAP10, PNKD, PAX2, CPOX, ABCB7, TAZ, TIMM8A, GK, PDHA1, HCCS, NYX, FRMD7, OTC, RP2, PRPF8, AGPS, PRPF31, PUS1, D2HGDH, CA4, PITPNM3, ALG3, STRA6, MYO7A, RNASEL, PPARGC1B, UCP3, UCP1, GJA3, PHOX2A, SQSTM1, GUCA1A, ETHE1, MPI, EYS, TYMP, ALG6, GAD1, SLC35A1, RIMS1, SCO2, LCA5, TAP1, CISD2, C1QTNF5, DMGDH, AMT, GLDC, GCSH, PINK1, HMGCS2, PCCA, PCCB, PARK7, GLUD1, B4GALT1, ALG12, SPG7, COQ2, UCP2, NDUFA13, GRN, ALG2, FSCN2, ALG8, UNG, AP3B1, MEF2A, CERKL, RGS9, ALG1, ATIC, ALG9, COG7, PDP1, DPM1, HADHB, FLVCR1, GFM1, MPDU1, PLOD2, IQCB1, SLC25A22, TK2, SECISBP2, TOPORS, ACADSB, CTSD, POLG2, DNAJC19, REEP1, ALDH2, SEMA4A, HTRA2, KCNV2, SNRNP200, CABP4, GNAT1, CACNA2D4, MRPS16, TSFM, PRCD, RD3, TUFM, CRTAP, PNPLA2, HAX1, SLC25A3, P3H1, TUSC3, DARS2, COG8, COG1, ACAD8, RARS2, GYS1, TUBA1A, MRPS22, CYCS, RFT1, COQ8A, SUCLA2, STXBP1, SLC9A3R1, SLC39A13, SDHB, PLOD3, RPL35A, AK1, SOD2, RDH12, COX4I2, SPR, GATM, GAMT, ADAM9, ENO3, LDHA, PGM1, DPM3, KLHL7, SLC25A12, TMEM126A, TLR3, PHKG2, GFER, PDE6C, ABAT, TRPM1, TSPAN12, CAVIN1, LRAT, GRK1, PCARE, GCKR, GPI, IMPG2, CNGA1, CYP24A1, G6PC, PYGL, NUBPL, NDUFA10, TAT, FAM161A, FYCO1, XPNPEP3, MTPAP, MSRB3, GNAT2, TTC19, HSD3B2, CCDC28B, HMGCL, NDUFAF1, PCK2, FAH, PHKA2, RS1, NFU1, CNGB1, RGR, CCDC39, PDE6A, GUCA1B, SLC24A1, SARS2, SP7, DHDDS, MERTK, SERPINF1, PRPF6, HAGH, TMEM70, ACAT2, HPS3, HPS4, HPS5, HPS6, BLOC1S3, HP, CAT, ALDH6A1, PDHB, LDHB, DIABLO, GPX1, ACSF3, BOLA3, DGUOK, DNM1L, HPS1, GOT1, ALDH18A1, AGK, COX14, NDUFA9, GPD1, NDUFB3, LIAS, C8orf37, HARS, BBS1, BBS4, BBS10, BBS9, MKS1, BBS12, BBS5, BBS7, CYP4V2, PPP2R1B, PRKN, PMM2, MGAT2, SLC25A20, SLC22A5, SIX6, CYP27A1, ASS1, CNGA3, SLC3A1, COX6B1, FASTKD2, LRPPRC, GLYCTK, FXN, GALK1, GALE, GALT, GCDH, ETFDH, ETFA, ETFB, GBE1, PYGM, PFKM, CYBA, HK1, CBS, L2HGDH, NAGS, SLC25A15, TNFRSF11B, ALDH4A1, IVD, OXCT1, GALC, DLAT, SUCLG1, MLYCD, MAN2B1, MANBA, DBT, HIBCH, CYB5A, CYB5R3, MUT, MMAA, MMAB, MCEE, NDUFAF5, NDUFS2, NDUFS6, NDUFV2, NDUFV1, NDUFS1, NDUFAF4, NDUFA11, NDUFA1, NDUFAF3, SDHAF1, MOCS1, MOCS2, SGSH, NAGLU, HGSNAT, GNS, GALNS, GUSB, CHAT, CPT1A, ISCU, NDUFAF6, NDUFS3, NDUFS7, NDUFS8, SURF1, COX15, NDUFA2, CTSA, NME1, MPV17, GRM6, OAT, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, AGXT, GIF, CUBN, PAH, QDPR, PTS, PGAM2, PHKB, ACOX1, CYP27B1, CTSK, ALDH7A1, NT5C3A, SLC35C1, PHYH, AK2, LPIN1, HEXB, SARDH, ALDH3A2, ALDH5A1, SUOX, GM2A, HEXA, TCN2, ABHD5, LMBRD1, MMADHC, XDH, ABCD1, BCOR, SLC9A6, AMER1, ACSL4, PHKA1, MAOA, AIFM1, DDOST, DHODH, IDH3B, NDUFA12, ACO2, MRPL3, COQ6, PDSS1, PDSS2, COQ9, CDH23, MTO1, WHRN, SLC26A4, FBN1, CYP11B2, MECP2, SMPD1, CRB1, CRX, GUCY2D, IMPDH1, PDE6B, PROM1, RHO, RLBP1, RPE65, RPGR, RPGRIP1, SAG, TULP1, VCP, FH, OPA3, RAF1, HADHA, PANK2, SDHC, CRYAB, MFN2, SLC25A13, ALAS2, KIF1B, NDUFAF2, RRM2B, FOXRED1, CYP11B1, AFG3L2, GARS, GCK, SLC25A4, SLC25A19, HSPD1, NDUFS4, POLG, DLD, AASS, DSP, PRPH2, ME2, SHH, PCDH15, NPHP4, USH2A, TRIM32, TTC8, CLRN1, CEP290, ADGRV1, MKKS, NPHP1, NPHP3, ARL6, KCNJ13, TMEM67, NHS, HPRT1, CNGB3, CYP1B1, OTX2, NDP, MFRP, CACNA1F, JAG1, ABCA4, PITX2, ELOVL4, FOXC1, OCRL, HSD17B10, GNE, SRD5A3, ATP6V0A2, PRODH, CC2D2A, GLB1, GNPTAB, PSAP, COMT, WFS1, DTNBP1, CLCN7, PYCR1, CASP8, TRMU, ABCB6, KRT5, OPA1, CPT2, CPS1, HSD17B4, AMACR, MTRR, SLC16A1, ABCA12, INPP5E, TNFRSF11A, GPR143, OPTN, RP1, EYA4, PDZD7, SLC37A4, ELN, TYR, MC1R, RET, MTR, HNF1B, LEMD3, SDHAF2, TUBB3, PITX3, TGFBI, RILP, PSEN1, RB1, CHM, TLR4, ELAC2, ZEB1, TGFB1, PAX6, WT1, SLC45A2, AMN, SOST, APP, SLC34A1, VSX1, OCA2, PRKCG, STAT1, STAR, KRT3, KRT12, GPD2, EFEMP1, SNCB, COL5A2, COL5A1, MEN1, WWOX, FZD4, KIF21A, RDH5, TIMP3, MYOC, OGG1, STAT3, RPS14, LMX1B, SEPT9, TMEM127, PPOX, ZFHX3, FECH, RP9, SLC22A4, HESX1, ANKRD26, NCOA4, CYP17A1, OGDH, ALMS1, CLN3, TPP1, GLRX5, SLC25A38, SOX2, ASL, APTX, BBS2, PDE6G, RP1L1, SPTLC2, KARS, IDH2, CDHR1, SCP2, CYP11A1, NRL, COL3A1, COL1A2, COL1A1, COL2A1, LRP5, PPARG, EYA1, FBLN5, TYRP1, RAX, MMACHC, SPATA7, NEUROD1, OPN1LW, HBB, HNF1A, OPN1MW, INVS, FOXL2, ADSL, GAA, C12orf65, TWNK, BEST1, BCS1L, BCKDHB, BCKDHA, B4GALT7, AUH, ATPAF2, ATP8B1, ATP7B, BTD, ATP7A, FKBP10, ATP5F1E, TYROBP, HLCS, UQCRB, ANKH, ARG1, UQCRQ, USH1C, GYS2, PC, FBP1, USH1G, ALDOB, ALDOA, YARS2, AIPL1, ZNF513, ACAT1, ACADVL, AGL, ACADS, ACADM, ACAD9, ACACA, ABHD12, ABCB4, ABCB11, AARS2, MCCC2, MCCC1, TP53, MUTYH, VHL, UBE3A, MTHFR, BRCA1 Specificity 2 % Genes 64 %
FKBP10 Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. FKBP10 Specificity 100 % Genes 10 %
FKBP10 Sequence Analysis. By Baylor Miraca Genetics Laboratories in United States. FKBP10 Specificity 100 % Genes 10 %
FKBP10 Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. FKBP10 Specificity 100 % Genes 10 %
Low Bone Mass Panel (MitomeNGS). By Baylor Miraca Genetics Laboratories in United States. COL5A2, COL5A1, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1, SLC9A3R1, SLC39A13, PLOD3, SP7, SERPINF1, FBN1, TNFRSF11A, SLC34A1, COL3A1, COL1A2, COL1A1, IFITM5, B4GALT7 , (...) View the complete list with 2 more genes Panel GTR000511543 complete gene list COL5A2, COL5A1, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1, SLC9A3R1, SLC39A13, PLOD3, SP7, SERPINF1, FBN1, TNFRSF11A, SLC34A1, COL3A1, COL1A2, COL1A1, IFITM5, B4GALT7, FKBP10, ALPL Specificity 32 % Genes 64 %
Congenital Contractures Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States. MYH8, ERCC6, ERBB3, PIP5K1C, SCARF2, PSMB8, RIPK4, CHMP1A, ECEL1, ZMPSTE24, PITX1, MYBPC1, ZBTB42, CNTNAP1, ADCY6, ADGRG6, GLDN, SLC18A3, PIEZO2, MYH3 , (...) View the complete list with 37 more genes Panel GTR000558813 complete gene list MYH8, ERCC6, ERBB3, PIP5K1C, SCARF2, PSMB8, RIPK4, CHMP1A, ECEL1, ZMPSTE24, PITX1, MYBPC1, ZBTB42, CNTNAP1, ADCY6, ADGRG6, GLDN, SLC18A3, PIEZO2, MYH3, TNNT3, NEK9, SLC5A7, TNNI2, KLHL41, GLE1, CHST14, FBN2, SKI, ANTXR2, NALCN, ZC4H2, CHRNG, CHRNB1, CHRND, CHRNA1, MUSK, MYH2, TPM2, CNTN1, ACTA1, TPM3, UBA1, LMNA, DNM2, RAPSN, NEB, DOK7, CHRNE, CHAT, ALG2, PLOD2, SLC39A13, PLOD3, FBN1, COL3A1, FKBP10 Specificity 2 % Genes 10 %
Osteogenesis Imperfecta and Genetic Bone Disorders Panel. By Collagen Diagnostic Laboratory University of Washington in United States. GORAB, B3GAT3, NBAS, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, XYLT2, SPARC, TAPT1, PLS3, MBTPS2, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1 , (...) View the complete list with 10 more genes Panel GTR000525804 complete gene list GORAB, B3GAT3, NBAS, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, XYLT2, SPARC, TAPT1, PLS3, MBTPS2, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1, PLOD3, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, B4GALT7, FKBP10, ALPL Specificity 37 % Genes 100 %
Osteogenesis Imperfecta (FKBP10 gene related). By Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital in New Zealand. FKBP10 Specificity 100 % Genes 10 %
FKBP10 - Osteogenesis imperfecta type 6. By Centre of Molecular Diseases (CMM) CHUV in Switzerland. FKBP10 Specificity 100 % Genes 10 %
Skeletal Dysplasia Panel, Sequencing (39 Genes) and Deletion/Duplication (36 Genes). By ARUP Laboratories, Molecular Genetics and Genomics in United States. TRIP11, SLC35D1, LIFR, FLNB, DLL3, ARSE, NEK1, DYNC2H1, EVC2, EVC, IFT80, TTC21B, SERPINH1, GNPAT, WDR19, SOX9, COMP, POR, EBP, WDR35 , (...) View the complete list with 19 more genes Panel GTR000522271 complete gene list TRIP11, SLC35D1, LIFR, FLNB, DLL3, ARSE, NEK1, DYNC2H1, EVC2, EVC, IFT80, TTC21B, SERPINH1, GNPAT, WDR19, SOX9, COMP, POR, EBP, WDR35, LBR, FLNA, HSPG2, FGFR1, TRPV4, SLC26A2, PEX7, FGFR2, RUNX2, FGFR3, PPIB, AGPS, CRTAP, P3H1, COL1A2, COL1A1, COL2A1, FKBP10, ALPL Specificity 18 % Genes 64 %
Skeletal Dysplasia Panel, Sequencing (39 Genes) and Deletion/Duplication (36 Genes), Fetal. By ARUP Laboratories, Molecular Genetics and Genomics in United States. TRIP11, SLC35D1, LIFR, FLNB, DLL3, ARSE, NEK1, DYNC2H1, EVC2, EVC, IFT80, TTC21B, SERPINH1, GNPAT, WDR19, SOX9, COMP, POR, EBP, WDR35 , (...) View the complete list with 19 more genes Panel GTR000522272 complete gene list TRIP11, SLC35D1, LIFR, FLNB, DLL3, ARSE, NEK1, DYNC2H1, EVC2, EVC, IFT80, TTC21B, SERPINH1, GNPAT, WDR19, SOX9, COMP, POR, EBP, WDR35, LBR, FLNA, HSPG2, FGFR1, TRPV4, SLC26A2, PEX7, FGFR2, RUNX2, FGFR3, PPIB, AGPS, CRTAP, P3H1, COL1A2, COL1A1, COL2A1, FKBP10, ALPL Specificity 18 % Genes 64 %
Osteogenesis Imperfecta & Low Bone Mass Disorders Panel. By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States. DMP1, SLC34A3, ENPP1, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, FGF23, PHEX, CASR, PPIB, PLOD2, CRTAP, P3H1, SP7 , (...) View the complete list with 7 more genes Panel GTR000530009 complete gene list DMP1, SLC34A3, ENPP1, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, FGF23, PHEX, CASR, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 41 % Genes 100 %
Osteogenesis Imperfecta, autosomal recessive-Bruck syndrome 1. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-FKBP10. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis imperfecta type XI (sequence analysis of FKBP10 gene). By CGC Genetics in Portugal. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis imperfecta (NGS panel for 16 genes). By CGC Genetics in Portugal. CREB3L1, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, IFITM5, FKBP10 Specificity 69 % Genes 100 %
Osteogenesis Imperfecta via FKBP10 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. FKBP10 Specificity 100 % Genes 10 %
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics in United States. TGDS, DDX59, COL27A1, SULF1, NPPC, TXNL4A, TBX4, RASGRP2, KIF22, ADAMTS17, ACAN, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, GHSR, TBX6, XYLT1 , (...) View the complete list with 238 more genes Panel GTR000558369 complete gene list TGDS, DDX59, COL27A1, SULF1, NPPC, TXNL4A, TBX4, RASGRP2, KIF22, ADAMTS17, ACAN, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, GHSR, TBX6, XYLT1, IHH, BHLHA9, SMOC1, WNT3, BMP2, NPR2, PCYT1A, SLCO2A1, MMP9, INPPL1, SNX10, MMP13, EOGT, DDR2, TBX3, HDAC4, MEOX1, MATN3, TRAPPC2, GDF5, PTHLH, HPGD, RBPJ, DOCK6, LFNG, HES7, MMP2, MESP2, WISP3, SF3B4, DMP1, SLC34A3, ENPP1, FAM111A, CCDC8, OBSL1, ORC4, ORC6, CDT1, CDC6, ORC1, ALX3, TCF12, ERF, MEGF8, BMPER, PTDSS1, PDE4D, CUL7, LRP4, ARSE, WDR60, NEK1, IRF6, CCNQ, WNT7A, TBX15, ROR2, HOXA13, ESCO2, DYNC2H1, RIN2, WNT5A, CEP120, SRCAP, AFF4, TCTN3, SMARCAL1, MGP, EXT1, EXT2, GDF3, ALX1, FREM1, HOXA11, TBXAS1, FERMT3, DHCR24, EIF2AK3, GREM1, IFT122, B3GALT6, MYCN, EVC2, EVC, IFT80, TTC21B, GORAB, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, SH3BP2, ASXL1, EFTUD2, EFNB1, EP300, TBX5, SALL4, ALX4, LHX4, FGF10, RIPK4, ZMPSTE24, PITX1, PIEZO2, WDR19, BMPR1B, CDH3, IFT140, GDF6, TP63, GLI3, NFIX, ACVR1, ZNF469, CHST14, TNXB, FKBP14, FBN2, SKI, TGFBR2, TGFBR1, DYM, ADAMTSL2, PCNT, SOX9, COMP, TWIST1, MSX2, RAB23, NSDHL, EBP, PTH1R, CANT1, WDR35, POLR1D, CHSY1, TCOF1, POLR1C, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, SALL1, LBR, FGD1, ANKRD11, PIGV, FLNA, HSPG2, ANO5, FGF23, PHEX, PROK2, SHOX, FGFR1, TRPV4, SLC26A2, PEX7, ADAMTS2, PRKAR1A, TRPS1, ADAMTS10, RAB33B, TRIP11, SLC35D1, LIFR, FLNB, GALNT3, ARHGAP31, ACP5, DLL3, NKX3-2, IMPAD1, CHST3, HOXD13, GPC6, SBDS, GPC3, NSD1, NIPBL, SMC1A, SMC3, RAD21, HDAC8, FGFR2, VDR, RUNX2, RMRP, PLOD1, CREBBP, COL10A1, FGFR3, COL5A2, COL5A1, LMX1B, TNFRSF11B, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CYP27B1, CTSK, AMER1, AGPS, SQSTM1, PLOD2, CRTAP, P3H1, COG1, SLC39A13, SP7, SERPINF1, DHODH, FBN1, SHH, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL3A1, COL1A2, COL1A1, COL2A1, LRP5, IFITM5, B4GALT7, FKBP10, TYROBP, ANKH, ALPL, RECQL4 Specificity 4 % Genes 91 %
Osteogenesis Imperfecta and Hypophosphatasia (HPP) Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics in United States. CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 58 % Genes 100 %
Osteogenesis Imperfecta and Hypophosphatasia (HPP), and Inherited Hypophosphatemic Rickets Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics in United States. DMP1, SLC34A3, ENPP1, CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, FGF23, PHEX, PPIB, CYP27B1, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2 , (...) View the complete list with 5 more genes Panel GTR000552568 complete gene list DMP1, SLC34A3, ENPP1, CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, FGF23, PHEX, PPIB, CYP27B1, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 44 % Genes 100 %
Osteogenesis imperfecta Comprehensive panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, CREB3L1, P4HB, SEC24D , (...) View the complete list with 4 more genes Panel GTR000559322 complete gene list SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, CREB3L1, P4HB, SEC24D, LRP5, IFITM5, FKBP10, ALPL Specificity 46 % Genes 100 %
Osteogenesis imperfecta Deletion / Duplication panel - Recessive. By Connective Tissue Gene Tests in United States. CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, LRP5, FKBP10, ALPL Specificity 48 % Genes 82 %
Osteogenesis imperfecta Deletion / Duplication panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1 , (...) View the complete list with 4 more genes Panel GTR000559365 complete gene list CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 46 % Genes 100 %
Osteogenesis imperfecta NGS panel - Recessive. By Connective Tissue Gene Tests in United States. CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, LRP5, FKBP10, ALPL Specificity 48 % Genes 82 %
Osteogenesis imperfecta Comprehensive panel - Recessive. By Connective Tissue Gene Tests in United States. CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, LRP5, FKBP10, ALPL Specificity 48 % Genes 82 %
Osteogenesis imperfecta NGS panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1 , (...) View the complete list with 4 more genes Panel GTR000559438 complete gene list CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, TAPT1, PLS3, MBTPS2, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 46 % Genes 100 %
FKBP10-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis imperfecta and osteoporosis - different panels. By Institute of Human Genetics Cologne University in Germany. MMP2, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5 , (...) View the complete list with 3 more genes Panel GTR000558418 complete gene list MMP2, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 48 % Genes 100 %
Osteogenesis imperfecta panel, autosomal recessive. By Centogene AG - the Rare Disease Company in Germany. SERPINH1, BMP1, PPIB, PLOD2, CRTAP, P3H1, SP7, FKBP10 Specificity 75 % Genes 55 %
Osteogenesis imperfecta type 11. By Centogene AG - the Rare Disease Company in Germany. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis imperfecta type XI. By Centogene AG - the Rare Disease Company in Germany. FKBP10 Specificity 100 % Genes 10 %
Congenital Myasthenic Syndromes and Arthrogryposis Panel. By CeGaT GmbH in Germany. ALG14, LRP4, PREPL, SYT2, MYH8, ERBB3, PIP5K1C, ECEL1, MYBPC1, CNTNAP1, ADCY6, ADGRG6, PIEZO2, MYH3, TNNT3, TNNI2, GLE1, CHST14, FBN2, NALCN , (...) View the complete list with 24 more genes Panel GTR000522473 complete gene list ALG14, LRP4, PREPL, SYT2, MYH8, ERBB3, PIP5K1C, ECEL1, MYBPC1, CNTNAP1, ADCY6, ADGRG6, PIEZO2, MYH3, TNNT3, TNNI2, GLE1, CHST14, FBN2, NALCN, ZC4H2, CHRNG, SNAP25, CHRNB1, CHRND, CHRNA1, AGRN, GFPT1, MUSK, COLQ, PLEC, SYNE1, TPM2, LAMB2, SCN4A, DNM2, RAPSN, DOK7, CHRNE, DPAGT1, CHAT, ALG2, PLOD2, FKBP10 Specificity 3 % Genes 10 %
Chondrodysplasia punctata Panel. By CeGaT GmbH in Germany. GORAB, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, ANO5, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, ATP6V0A2, PYCR1, COL1A2, COL1A1, LRP5, IFITM5 , (...) View the complete list with 2 more genes Panel GTR000527962 complete gene list GORAB, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, ANO5, TNFRSF11B, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, ATP6V0A2, PYCR1, COL1A2, COL1A1, LRP5, IFITM5, B4GALT7, FKBP10 Specificity 46 % Genes 91 %
FKBP10 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. FKBP10 Specificity 100 % Genes 10 %
OI panel 2. By Connective Tissue Laboratory Ghent University Hospital in Belgium. B3GALT6, CREB3L1, P4HB, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, XYLT2, SPARC, TAPT1, MBTPS2, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, FKBP10 Specificity 48 % Genes 82 %
OSTEOGENESIS IMPERFECTA. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. SERPINH1, BMP1, ANO5, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10 Specificity 65 % Genes 82 %
NGS panel - Osteogenesis Imperfecta and related disorders. By Genome Diagnostics VU University Medical Center in Netherlands. CREB3L1, SERPINH1, WNT1, BMP1, TMEM38B, TAPT1, PLS3, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, FKBP10, ALPL Specificity 58 % Genes 100 %
Osteogenesis Imperfecta and Decreased Bone Density: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. MAFB, MMP2, DMP1, SLC34A3, CLCN5, ENPP1, NOTCH2, TREM2, GORAB, SERPINH1, GNAS, ZMPSTE24, ANO5, FGF23, PHEX, CASR, LMNA, PPIB, PLOD2, CRTAP , (...) View the complete list with 14 more genes Panel GTR000512609 complete gene list MAFB, MMP2, DMP1, SLC34A3, CLCN5, ENPP1, NOTCH2, TREM2, GORAB, SERPINH1, GNAS, ZMPSTE24, ANO5, FGF23, PHEX, CASR, LMNA, PPIB, PLOD2, CRTAP, P3H1, SP7, ATP6V0A2, PYCR1, TNFRSF11A, COL1A2, COL1A1, LRP5, IFITM5, B4GALT7, FKBP10, TYROBP, ANKH, ALPL Specificity 21 % Genes 64 %
Skeletal Dysplasia: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. SULF1, RASGRP2, KIF22, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, IHH, WNT3, BMP2, NPR2, MMP9, MAFB, MMP13, DLX3, DDR2, TBX3, HDAC4 , (...) View the complete list with 143 more genes Panel GTR000512649 complete gene list SULF1, RASGRP2, KIF22, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, IHH, WNT3, BMP2, NPR2, MMP9, MAFB, MMP13, DLX3, DDR2, TBX3, HDAC4, MATN3, GDF5, PTHLH, HPGD, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, GALNT3, ARHGAP31, ACP5, NKX3-2, CHST3, HOXD13, GPC6, MMP2, WISP3, DMP1, SLC34A3, CLCN5, ENPP1, TBCE, OBSL1, CUL7, LRP4, NEK1, ICK, WNT7A, TBX15, ROR2, ESCO2, DYNC2H1, WNT5A, TCTN3, NOTCH2, SMARCAL1, MGP, EXT1, EXT2, TBXAS1, FERMT3, DHCR24, EIF2AK3, GREM1, TREM2, IFT122, B3GALT6, MYCN, EVC2, EVC, IFT80, KIF7, RPGRIP1L, THPO, GORAB, SERPINH1, GNAS, TBX5, SALL4, FGF10, ZMPSTE24, PITX1, BMPR1B, SH3PXD2B, CDH3, IFT140, TP63, GLI3, CHST14, DYM, PCNT, SOX9, COMP, PTH1R, CANT1, WDR35, CHSY1, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, SALL1, PIGV, FLNA, HSPG2, ANO5, FGF23, PHEX, CASR, SHOX, FGFR1, LMNA, TRPV4, TMEM216, SLC26A2, PRKAR1A, CDKN1C, NIPBL, FGFR2, RUNX2, PTPN11, COL10A1, FGFR3, MKS1, TNFRSF11B, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, PLOD2, CRTAP, P3H1, SLC39A13, SLC25A12, SP7, FBN1, SHH, CEP290, TMEM67, ATP6V0A2, CC2D2A, CLCN7, PYCR1, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A2, COL1A1, COL2A1, LRP5, IFITM5, B4GALT7, FKBP10, TYROBP, ANKH, ALPL, RECQL4 Specificity 5 % Genes 64 %
Amelogenesis Imperfecta NGS Panel. By Fulgent Genetics Fulgent Genetics in United States. WDR72, MMP20, KLK4, ENAM, FAM83H, DLX3, AMELX, FAM20A, SERPINH1, BMP1, DSPP, PPIB, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, IFITM5, FKBP10 Specificity 45 % Genes 82 %
Skeletal Dysplasias NGS panel. By Fulgent Genetics Fulgent Genetics in United States. SULF1, RASGRP2, KIF22, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, IHH, WNT3, BMP2, NPR2, MMP9, MAFB, MMP13, DLX3, DDR2, TBX3, HDAC4 , (...) View the complete list with 141 more genes Panel GTR000515853 complete gene list SULF1, RASGRP2, KIF22, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, IHH, WNT3, BMP2, NPR2, MMP9, MAFB, MMP13, DLX3, DDR2, TBX3, HDAC4, MATN3, GDF5, PTHLH, HPGD, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, GALNT3, ARHGAP31, ACP5, NKX3-2, CHST3, HOXD13, GPC6, MMP2, WISP3, DMP1, SLC34A3, CLCN5, ENPP1, TBCE, OBSL1, CUL7, LRP4, NEK1, ICK, WNT7A, TBX15, ROR2, ESCO2, DYNC2H1, WNT5A, NOTCH2, SMARCAL1, MGP, EXT1, EXT2, TBXAS1, FERMT3, DHCR24, EIF2AK3, GREM1, TREM2, IFT122, B3GALT6, MYCN, EVC2, EVC, IFT80, KIF7, RPGRIP1L, THPO, GORAB, SERPINH1, GNAS, TBX5, SALL4, FGF10, ZMPSTE24, PITX1, BMPR1B, SH3PXD2B, CDH3, IFT140, TP63, GLI3, CHST14, DYM, PCNT, SOX9, COMP, PTH1R, CANT1, WDR35, CHSY1, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, SALL1, PIGV, FLNA, HSPG2, ANO5, FGF23, PHEX, CASR, FGFR1, LMNA, TRPV4, TMEM216, SLC26A2, PRKAR1A, CDKN1C, NIPBL, FGFR2, RUNX2, PTPN11, COL10A1, FGFR3, MKS1, TNFRSF11B, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, PLOD2, CRTAP, P3H1, SLC39A13, SLC25A12, SP7, FBN1, SHH, CEP290, TMEM67, ATP6V0A2, CC2D2A, CLCN7, PYCR1, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A2, COL1A1, COL2A1, LRP5, IFITM5, B4GALT7, FKBP10, TYROBP, ANKH, ALPL, RECQL4 Specificity 5 % Genes 64 %
FKBP10. By Fulgent Genetics Fulgent Genetics in United States. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta Panel. By Blueprint Genetics in Finland. SLC34A3, CLCN5, B3GAT3, CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, MBTPS2, FGF23, PHEX, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1 , (...) View the complete list with 7 more genes Panel GTR000552815 complete gene list SLC34A3, CLCN5, B3GAT3, CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, MBTPS2, FGF23, PHEX, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, LRP5, IFITM5, B4GALT7, FKBP10, ALPL Specificity 41 % Genes 100 %
Arthrogryposes Panel. By Blueprint Genetics in Finland. CHUK, ERCC5, VIPAS39, VPS33B, DHCR24, MYH8, ERCC6, ERBB3, RIPK4, ECEL1, MYBPC1, ZBTB42, CNTNAP1, ADGRG6, PIEZO2, MYH3, TNNT3, TNNI2, GLE1, TGFB3 , (...) View the complete list with 49 more genes Panel GTR000552659 complete gene list CHUK, ERCC5, VIPAS39, VPS33B, DHCR24, MYH8, ERCC6, ERBB3, RIPK4, ECEL1, MYBPC1, ZBTB42, CNTNAP1, ADGRG6, PIEZO2, MYH3, TNNT3, TNNI2, GLE1, TGFB3, CHST14, FBN2, FLVCR2, NALCN, TSEN2, EXOSC3, ZC4H2, CHRNG, KAT6B, CASK, TSEN54, COL6A2, CHRNB1, CHRND, CHRNA1, AGRN, GFPT1, MUSK, COLQ, VRK1, BIN1, MTM1, TNNT1, MYH2, TPM2, CFL2, ACTA1, TPM3, KLHL40, SELENON, FHL1, EGR2, MPZ, TRPV4, RAPSN, NEB, FKTN, DOK7, CHRNE, GBA, DPAGT1, PMM2, GBE1, CHAT, SCO2, PLOD2, TK2, RARS2, FKBP10 Specificity 2 % Genes 10 %
Skeletal Dysplasias Core Panel. By Blueprint Genetics in Finland. ACAN, PAPSS2, DVL1, XYLT1, IHH, NPR2, MMP9, INPPL1, MATN3, TRAPPC2, GDF5, ADAMTS10, TRIP11, LIFR, FLNB, ACP5, DLL3, CHST3, WISP3, SLC34A3 , (...) View the complete list with 91 more genes Panel GTR000558786 complete gene list ACAN, PAPSS2, DVL1, XYLT1, IHH, NPR2, MMP9, INPPL1, MATN3, TRAPPC2, GDF5, ADAMTS10, TRIP11, LIFR, FLNB, ACP5, DLL3, CHST3, WISP3, SLC34A3, ENPP1, OBSL1, RNU4ATAC, ORC4, ORC6, CDT1, CDC6, ORC1, CUL7, ARSE, NEK1, ROR2, ESCO2, DYNC2H1, WNT5A, CSPP1, IFT172, SMARCAL1, DHCR24, EIF2AK3, B3GALT6, EVC2, EVC, IFT80, TTC21B, SERPINH1, BMP1, PLS3, GNPAT, WDR19, BMPR1B, LTBP2, IFT140, DYM, ADAMTSL2, PCNT, SOX9, COMP, EBP, PTH1R, CANT1, WDR35, KAT6B, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, LBR, FLNA, HSPG2, FGF23, PHEX, SHOX, FGFR1, TRPV4, SLC26A2, PEX7, SBDS, SMAD4, CDKN1C, FGFR2, VDR, RUNX2, RMRP, COL10A1, FGFR3, LMX1B, TNFRSF11B, PPIB, TCIRG1, CA2, FAM20C, CYP27B1, CTSK, AGPS, PLOD2, CRTAP, P3H1, SLC39A13, SERPINF1, CLCN7, TNFRSF11A, TGFB1, COL1A2, COL1A1, COL2A1, LRP5, FKBP10, ANKH, ALPL Specificity 9 % Genes 82 %
Comprehensive Skeletal Dysplasias and Disorders Panel. By Blueprint Genetics in Finland. CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, BHLHA9, WDR34, FAM83H , (...) View the complete list with 226 more genes Panel GTR000558787 complete gene list CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, BHLHA9, WDR34, FAM83H, BMP2, NPR2, PCYT1A, SLCO2A1, MMP9, MAFB, INPPL1, SNX10, MMP13, DLX3, EOGT, DDR2, TBX3, MATN3, TRAPPC2, GDF5, PTHLH, RBPJ, DOCK6, TRPS1, ADAMTS10, RAB33B, TRIP11, SLC35D1, LIFR, FLNB, FAM20A, GALNT3, ARHGAP31, ACP5, DLL3, NKX3-2, IMPAD1, CHST3, HOXD13, GPC6, MMP2, MESP2, WISP3, SF3B4, DMP1, SLC34A3, CLCN5, ENPP1, FAM111A, OBSL1, ORC4, ORC6, CDT1, CDC6, ORC1, ALX3, TCF12, CDC45, BMPER, PTDSS1, PDE4D, CUL7, LRP4, ARSE, WDR60, NEK1, TBX15, ROR2, HOXA13, ESCO2, DYNC2H1, WNT5A, CSPP1, IFT172, TCTN3, PGM3, NOTCH2, SMARCAL1, MGP, EXT1, EXT2, AKT1, VIPAS39, DHCR24, EIF2AK3, IFT122, B3GALT6, MYCN, PIK3CA, EVC2, EVC, IFT80, IFT43, KIF7, TTC21B, SLC29A3, BGN, B3GAT3, SERPINH1, WNT1, BMP1, TMEM38B, PLS3, GJA1, GNAS, GNPAT, SH3BP2, EFTUD2, EFNB1, EP300, ALX4, STAMBP, KMT2A, WDR19, TGFB3, BMPR1B, SH3PXD2B, LTBP2, IFT140, TP63, GLI3, EZH2, NFIX, ACVR1, CHST14, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, DYM, ADAMTSL2, PCNT, SOX9, COMP, TWIST1, MSX2, POR, NSDHL, EBP, FANCB, PTH1R, CANT1, WDR35, KAT6B, POLR1D, CHSY1, TCOF1, POLR1C, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, LBR, SETBP1, ANKRD11, FLNA, HSPG2, ANO5, FGF23, PHEX, CASR, SHOX, FGFR1, RNU4ATAC, NF1, LMNA, TRPV4, SLC26A2, PEX7, PRKAR1A, SBDS, SMAD4, CDKN1C, NSD1, NIPBL, SMC1A, SMC3, RAD21, HDAC8, FGFR2, VDR, RUNX2, RMRP, PTPN11, IDS, CREBBP, COL10A1, FANCC, FGFR3, ARSB, LMX1B, TNFRSF11B, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CYP27B1, CTSK, AMER1, AIFM1, AGPS, PLOD2, CRTAP, P3H1, SLC39A13, SP7, SERPINF1, FBN1, ATP6V0A2, CLCN7, PYCR1, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A2, COL1A1, COL2A1, LRP5, B4GALT7, FKBP10, TYROBP, ANKH, ALPL, RECQL4 Specificity 5 % Genes 91 %
Skeletal Dysplasia with Abnormal Mineralization Panel. By Blueprint Genetics in Finland. SNX10, GALNT3, SLC34A3, CLCN5, ENPP1, PTDSS1, MGP, PLS3, SOX9, FGF23, PHEX, CASR, VDR, COL5A2, COL5A1, TNFRSF11B, PPIB, CYP27B1, PLOD2, CRTAP , (...) View the complete list with 12 more genes Panel GTR000552636 complete gene list SNX10, GALNT3, SLC34A3, CLCN5, ENPP1, PTDSS1, MGP, PLS3, SOX9, FGF23, PHEX, CASR, VDR, COL5A2, COL5A1, TNFRSF11B, PPIB, CYP27B1, PLOD2, CRTAP, P3H1, SLC39A13, SERPINF1, FBN1, TNFRSF11A, COL3A1, COL1A2, COL1A1, B4GALT7, FKBP10, ANKH, ALPL Specificity 22 % Genes 64 %
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel. By Blueprint Genetics in Finland. IRS1, CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, IGFALS, BHLHA9 , (...) View the complete list with 288 more genes Panel GTR000561533 complete gene list IRS1, CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, IGFALS, BHLHA9, WDR34, FAM83H, BMP2, NPR2, PCYT1A, SLCO2A1, MMP9, MAFB, INPPL1, SNX10, MMP13, DLX3, EOGT, DDR2, IGF1R, TBX3, MATN3, IGF1, TRAPPC2, GDF5, PTHLH, RBPJ, DOCK6, TRPS1, ADAMTS10, RAB33B, TRIP11, SLC35D1, LIFR, FLNB, FAM20A, GALNT3, ARHGAP31, DLL3, NKX3-2, IMPAD1, CHST3, HOXD13, GPC6, MMP2, MESP2, WISP3, SF3B4, DMP1, SLC34A3, CLCN5, ENPP1, FAM111A, POC1A, LARP7, CCDC8, OBSL1, XRCC4, RNU4ATAC, ORC4, ORC6, CDT1, CDC6, ORC1, ALX3, TCF12, CDC45, CEP63, BMPER, PTDSS1, PDE4D, CUL7, LRP4, ARSE, WDR60, NEK1, CCNQ, TBX15, ROR2, HOXA13, ESCO2, DYNC2H1, RTTN, WNT5A, CSPP1, SRCAP, IFT172, TCTN3, PGM3, NOTCH2, SMARCAL1, MGP, STAT5B, EXT1, EXT2, AKT1, INSR, VIPAS39, DHCR24, EIF2AK3, IFT122, B3GALT6, MYCN, RBBP8, PIK3CA, EVC2, EVC, IFT80, IFT43, KIF7, TTC21B, SLC29A3, BGN, B3GAT3, CREB3L1, SEC24D, SERPINH1, WNT1, BMP1, TMEM38B, SPARC, PLS3, GJA1, GNAS, TRIM37, GNPAT, SH3BP2, EFTUD2, EFNB1, EP300, ALX4, LHX3, LHX4, TBX19, STAMBP, KMT2A, WDR19, TGFB3, BMPR1B, SH3PXD2B, LTBP2, IFT140, TP63, GLI3, EZH2, NFIX, ACVR1, CHST14, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, DYM, ADAMTSL2, ATR, PCNT, GLI2, CEP152, RRAS, RASA2, SOX9, COMP, TWIST1, MSX2, POR, NSDHL, SOX3, EBP, FANCB, MBTPS2, PTH1R, CANT1, WDR35, KAT6B, PEX19, PEX14, LZTR1, POLR1D, CHSY1, TCOF1, POLR1C, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, ACTG1, ACTB, LBR, SETBP1, FGD1, ANKRD11, FLNA, CENPJ, HSPG2, ANO5, FGF23, PHEX, GHR, GH1, POU1F1, CASR, SHOX, FGFR1, GHRHR, NF1, LMNA, TRPV4, SLC26A2, PEX7, PROP1, PRKAR1A, ACP5, SBDS, SMAD4, CDKN1C, NSD1, NIPBL, SMC1A, SMC3, CBL, RAD21, MAP2K2, RIT1, HDAC8, FGFR2, VDR, SOS1, SHOC2, RUNX2, RMRP, PTPN11, NRAS, MAP2K1, KRAS, IDS, HRAS, DHCR7, CREBBP, COL10A1, BRAF, FANCC, FGFR3, ARSB, COL5A2, COL5A1, LMX1B, HESX1, SOX2, TNFRSF11B, PPIB, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CYP27B1, CTSK, AMER1, AIFM1, AGPS, PLOD2, CRTAP, P3H1, SLC39A13, SP7, SERPINF1, FBN1, RAF1, OTX2, PITX2, ATP6V0A2, CLCN7, PYCR1, TNFRSF11A, LEMD3, TGFB1, SOST, COL3A1, COL1A2, COL1A1, COL2A1, LRP5, IFITM5, BCS1L, B4GALT7, FKBP10, TYROBP, ANKH, ALPL, RECQL4 Specificity 4 % Genes 100 %
Combined Skeletal Dysplasia/Osteogenesis Imperfecta Panel. By Insight Medical Genetics in United States. PAM16, INPPL1, ROR2, ESCO2, DYNC2H1, EVC2, EVC, IFT80, SERPINH1, WNT1, BMP1, TMEM38B, SOX9, TWIST1, COL11A1, FGFR1, SLC26A2, PEX7, FGFR2, FGFR3 , (...) View the complete list with 13 more genes Panel GTR000518899 complete gene list PAM16, INPPL1, ROR2, ESCO2, DYNC2H1, EVC2, EVC, IFT80, SERPINH1, WNT1, BMP1, TMEM38B, SOX9, TWIST1, COL11A1, FGFR1, SLC26A2, PEX7, FGFR2, FGFR3, PPIB, AGPS, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, COL2A1, IFITM5, FKBP10, ALPL Specificity 31 % Genes 91 %
BRUCKS SYNDROME (OSTEOGENESIS IMPERFECTA-CONGENITAL JOINT CONTRACTURES). By Laboratorio de Genetica Clinica SL in Spain. PLOD2, FKBP10 Specificity 50 % Genes 10 %
OSTEOGENESIS IMPERFECTA (AUTOSOMAL RECESSIVE). By Laboratorio de Genetica Clinica SL in Spain. SERPINH1, WNT1, BMP1, PPIB, CRTAP, P3H1, SP7, SERPINF1, FKBP10 Specificity 89 % Genes 73 %
Bruck Syndrome Type 1, Sequencing FKBP10 Gene. By Reference Laboratory Genetics in Spain. FKBP10 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Panel Massive Sequencing (NGS) 12 Genes. By Reference Laboratory Genetics in Spain. SERPINH1, BMP1, PPIB, PLOD2, CRTAP, P3H1, SP7, SERPINF1, COL1A2, COL1A1, IFITM5, FKBP10 Specificity 75 % Genes 82 %
Bruck Syndrome , Panel Massive Sequencing (NGS) FKBP10, PLOD2 Genes. By Reference Laboratory Genetics in Spain. PLOD2, FKBP10 Specificity 50 % Genes 10 %
Tempus xO assay. By Tempus Labs, Inc. in United States. SETD6, PIM3, MAP3K10, PDGFA, MAP3K11, PAK2, KHSRP, WASL, CASC11, GLIS1, NRG2, SOX21, SMARCC1, CUL4A, UTY, WNT9A, TEF, CHIC1, TRIM28, CDK11B , (...) View the complete list with 1693 more genes Panel GTR000558444 complete gene list SETD6, PIM3, MAP3K10, PDGFA, MAP3K11, PAK2, KHSRP, WASL, CASC11, GLIS1, NRG2, SOX21, SMARCC1, CUL4A, UTY, WNT9A, TEF, CHIC1, TRIM28, CDK11B, JUND, CKS2, FGF21, VGLL2, MAPK11, BMX, PBX3, KDM5D, PRRX2, GFRA4, ASCL5, VEGFD, SMARCD1, EPHA6, MAPK12, HDGFL3, SMYD2, TRIM24, E2F5, CDX1, RELB, PPP6C, ZNRF3, FOXQ1, TBC1D12, YEATS4, POU2F2, PDPK1, CES1, USP9Y, ICOSLG, NKX2-8, MTCP1, HOXD11, TLX1, CCDC6, CBFA2T3, OLIG2, HLF, MLLT6, TAL2, HOXC11, LMO2, RAP1GDS1, MDS2, LYL1, SFPQ, WIF1, TRIM33, MAPK3, GID4, ZNF703, MEF2B, AURKA, TOP1, MAP3K6, FGF4, SMARCA1, SUZ12, NCOR2, FGF19, HES1, RHOA, BCL2L1, H3F3A, KLF4, CDK13, BCL11B, HLA-A, NUTM2B, NUTM2A, SSX2, ETV4, TFEB, SSX4, NR4A3, MSI2, CREB3L2, TFE3, FOXO1, ETV1, BCL3, SET, BTG1, ADGRA2, ADGRL3, AHR, AFF1, ABCC1, AATK, ACVR2A, ACSL6, ACVR1B, ADAMTS20, ADGRB3, ADGRL2, PTPN6, PTPRD, RABEP1, PSPN, PTPN2, PTPN21, PTPRK, PTPRM, PTK2B, PTK2, PTGS2, RAD51AP1, PSIP1, PTPRG, PTTG1, PTGS1, PTPRR, RAD51B, PTPRJ, RBM14, RAD52, PTK7, PRSS8, PTK6, RAB25, SETD1B, SHB, RUNX3, RPS6KB1, SKIL, SGK1, RUVBL1, RIPK2, SETDB2, SGO2, SFRP1, RHOT1, SETD7, SLC22A3, SGO1, SF1, RNF40, SF3A1, RELA, RIPK1, SLC22A2, SHC4, SHC1, SETD4, SLC22A6, SH3GL1, ROCK2, SLC22A1, SKP2, SAV1, RSPO3, RHEB, RHOB, REC8, SETMAR, ROCK1, SETDB1, REL, SLC15A2, RPS6KB2, RPA1, SETD3, SETD9, RYK, RIPK3, SKOR1, RSPO2, TAOK3, SLC47A1, SMC2, SSTR3, SLC47A2, STAT6, SUV39H1, SMAD5, SSTR1, SMC6, STK36, TCF7L1, TEC, SMYD3, STARD3, SMYD5, SMC4, SUV39H2, TAOK2, SYK, TCL1A, SPDEF, SMC1B, TAOK1, SLCO2B1, TEAD3, STK19, SMARCA5, SSTR2, TEAD4, SPOPL, SP3, TAF1L, STYK1, SPEN, SLIT2, SOCS1, SLCO1A2, SMC5, TET3, SMYD4, TENM2, TEAD2, SP140L, SPI1, TERF1, STAT5A, SPRED2, SP140, TCF7, PRDM15, E2F1, CEBPB, AREG, PRKACB, PBX4, KAT5, FGF13, NFKBIB, PGF, SRMS, BBC3, SMURF1, FOSB, GUCY1A2, PHLPP1, SSTR4, ARTN, WNK2, INSRR, BUB3, CBX7, SHC3, IL13RA1, HES4, CEBPD, NFIC, IL9R, TCL1B, IL2RB, HDAC5, FKBP9, ZNF444, FGF22, ID4, SMYD1, RBMX, PRMT2, NFATC2, ZC3H12D, VGLL3, GSTT1, SPRY3, FOSL1, RBMXL1, GSK3A, ARHGAP10, WNT9B, NTF3, SPIB, SMARCD3, TNKS2, IL15RA, FGF11, RARG, VGLL4, SPRED3, SHC2, CARM1, ALKBH6, IL3RA, MAPK13, NRG4, CBX3, PDS5A, DACH2, BTG3, NKX2-4, HES2, ASCL2, MAPK14, SPOP, TFEC, SSX1, SS18, SOX8, SP100, SULT1A1, SMURF2, KMT5C, STAT4, SRGAP3, SPIC, SSX3, TBX2, ELOC, WNT11, TLR7, NSD3, WNT2B, ZNF668, ZNF471, ZC3H7B, TLK2, TLR8, WNT2, ZMYND8, WNT5B, WNT8B, TGFA, WNT7B, WWTR1, WNT16, TLR10, ZNF607, WISP1, YWHAB, WNT6, YWHAH, ZBTB33, XIRP2, XPO1, YES1, YY1, ZNF704, ZBTB7B, ZNF217, WAPL, TLX2, VHLL, VAV2, TNFRSF17, TRAF7, UBE2D2, TXK, TNK1, TRIB3, TRAF3IP3, TYRO3, UHRF2, TP53BP1, TLR9, TRRAP, TRIB2, TNFRSF14, UBE4A, TPTE, TOP2A, UGT1A4, TRAF1, VEGFB, UBE2D1, U2AF2, VGLL1, TMPRSS2, UBE2D4, TSHZ3, VAV3, TRIM66, TOP2B, VTCN1, UHRF1, PRMT5, PIK3C2G, PRDM10, PLAG1, PLCG1, PIK3R4, PRDM4, PRMT8, PRCC, PRMT3, PIK3C2B, PNRC1, PRKCI, PRDM14, PLK2, POU6F1, PREX2, PPP1R1C, PRDM11, PRDM7, PLAGL2, PRSS3, PIK3R3, PRDM6, PPFIA1, PPARD, PRMT6, POU5F1B, PIK3C2A, POU2AF1, PLK3, POU5F2, PIM1, PMAIP1, PRDM2, PRMT1, PLK1, POU5F1, PIM2, PRDM1, PIK3C3, PHLPP2, HLTF, HEY2, HIST1H3B, HIF1AN, HDAC1, HBEGF, HDGF, HDAC3, HDAC9, HEY1, GTPBP4, HIST1H1E, HDAC10, HIST1H4E, HDAC2, HIF1A, HDAC11, HCK, HDAC7, IL18RAP, AJUBA, JADE1, HOXD3, IKZF2, ID1, JUNB, IL1R2, IQGAP3, KDM2A, IKBIP, IL5RA, PVT1, PTPRB, KDM7A, IL1RAP, HOXD4, KAT8, KDM3B, ID3, KDM2B, KDM4D, IL12RB2, JAK1, KAT2A, JUN, KLF5, KDM4C, IRAK1, HOXA10, KDM1B, KAT7, HOXC10, INTS12, KMT5A, IRS4, HSPBAP1, JMJD7, IL1R1, KDM8, MAP3K21, JMJD8, ING4, HOXA9, IL20RA, HOXB3, KDM5B, KDM4B, IL6ST, JAZF1, ING1, IQGAP2, INPP4B, IL17RB, KDM3A, KLF12, KMT2E, IL3, IQGAP1, JMJD6, IFNLR1, ID2, IL22RA2, IL22RA1, IKZF3, HSP90AB1, HSP90AA1, HNRNPA3, KDM4A, ITPKB, IL20RB, JMJD4, JARID2, ARPC1B, BAZ1B, BAG4, LTK, ASPSCR1, APEX1, LRP1B, BAZ1A, LEF1, LGR6, LGR5, APH1A, LPP, LSM1, ARNT, BAZ2A, BCL2L11, BAZ2B, BACH2, LMO7, LMTK2, ASXL2, ARHGAP35, LMTK3, ARPC1A, BACH1, ATAD2, BCL2L2, AURKB, LMO1, ATF1, LATS1, BCAR3, ASCL3, ASCL4, LDB1, ASH2L, ATAD2B, LATS2, ARFRP1, LGR4, ARHGAP26, BABAM1, BCL2A1, MPG, BIRC8, MGA, MOB1B, MLLT11, MAP2K5, MINK1, MAP2K3, MAST1, MAPK6, MAP4K2, BPTF, BUB1, MAP3K13, MAST2, MDM4, MLLT10, MAML1, MATK, MAP3K9, MAP2K4, MAGED1, MAP4K3, BCL9, MAP4K5, BRD3, BTRC, MAP2K7, MOB1A, MRTFA, BIRC2, MAPK7, BTC, MCL1, MAP3K19, MAML3, MOS, MAP3K2, MAPK15, MAP3K12, BCLAF1, BRWD1, BRD7, MED12L, BRD8, EMSY, MAML2, BIRC5, BRD9, BID, MAP4, TIE1, ZNF521, TLK1, ZBTB5, WNT3A, ZNF639, YWHAZ, TLR6, WNT8A, YWHAQ, ZC3H12A, ZCCHC7, TPTE2, TNKS, UBE2D3, TLX3, TRAF2, MAPK4, BMI1, MLST8, MAP4K4, BCL7A, MAPK9, MED29, MRTFB, MAP3K5, BRD1, BRPF3, BTG2, MAD2L1, BRPF1, MAP3K15, MAP3K4, MAP4K1, MAU2, MAP2K6, NR4A1, NUTM2F, NUTM1, CAPRIN2, CHD5, MST1R, ODC1, MST1, CMPK1, NUTM2G, CHEK1, NUMBL, CHD9, CADM2, MSH4, CARD6, CHIC2, E2F3, DVL2, ELF2, ELF3, PHF1, EPHA7, FAT3, FEV, FGR, ETV3L, FGF6, FBXO8, ESPL1, ESCO1, EREG, FBXO11, ETS2, ETV7, EZH1, FGF7, FGF1, ESRRA, ERG, ETV3, FES, FER, FHIT, FEN1, EXTL1, FAT2, TENT5C, FGF18, FGF5, ETV2, ETS1, FGF2, FOXM1, FOXA3, FOXL1, FOXN3, FOXO4, FOXP4, FRS2, GABPA, FZR1, FOSL2, FYN, FOS, FRS3, FOXO3, FRK, GAB1, FUBP1, FLT3LG, NFKBIZ, NCOA2, CD274, NCOR1, CBX1, CEBPG, CDK15, NPPB, NEK11, CDK18, NCOA1, CD86, CDH10, MTDH, CD276, NFATC3, CDK1, NAB1, CDC42, CDK8, NEK4, CCND3, CDK10, CDKN1A, CDH20, NEK6, NEK7, NFIB, NKX3-1, CD1D, CD22, CDK3, CECR2, NFATC1, NQO1, CDKN3, NCK1, NKX2-3, MYB, CBX4, CDK20, CDH11, CEBPZ, CDH5, NEK5, CDK7, CDK2, CCNL1, CCNB3, CBX6, CDK14, CES2, CD28, NFATC4, CBX5, CD80, CDX2, CDC25C, CDK17, CDK9, NCOA3, NFKBID, NOTCH4, NCK2, IKBKE, IL18R1, NPR1, CDH2, CDC25B, NOTCH2NLA, CDC25A, NEK3, CCNE2, NFKBIE, NEK10, CDC20, MYBL1, NAB2, CBX8, CBFA2T2, MYOD1, GRB2, GPS2, GRK4, GSK3B, GRM8, GRK5, GRM3, GRB7, PTGIS, RAD54B, RAD54L, SSTR5, TCF7L2, PPM1D, POU6F2, NR4A2, PRKACA, MAD1L1, ALOX5, ZNF750, EPHB2, TLR2, SMAD7, MIPOL1, IL6R, IRF5, PGR, HMGA2, IRS1, IRF4, HMGA1, IRS2, IL4R, IL23R, GLCCI1, FKBP5, CREB1, CSNK1D, CD44, CHUK, ABCG2, PAK5, BAX, HSD3B1, HTR2A, TBL1X, RBM15, FOLH1, FOXA1, FOXA2, TRAF6, PIK3CG, CRKL, PIK3CB, MAPK1, GAB2, CRK, SPRY2, DOCK2, MAP3K14, IL17RC, PAX7, SEM1, SOX1, EPHB4, TRIB1, PPARA, PERP, SMAD1, ESR2, PRDM9, RBMXL2, CHD1, PAX1, RHOH, SP110, FGF16, DRD1, PRKAR1B, TAF15, EWSR1, ELP3, UBR5, AXIN1, ADRB1, SLC19A1, MYBL2, PTPRT, EGR1, ABI1, CRLF2, MLF1, INHBA, ARNT2, IKBKB, LCK, TLR5, XBP1, YAP1, CDK11A, CYP2B6, PHIP, ADAM17, KLF6, BCL10, CYP3A5, RRM1, NTF4, ESR1, SS18L1, STAG1, CRHR1, PEAR1, KMT2C, FGFR4, NTRK3, MYCL, ROS1, RPTOR, GNA13, EML4, BRD4, ARAF, NFE2L2, KEAP1, NRG1, CCNE1, IGF2, ELK1, BRD2, GLI1, STAT2, DACH1, MXD1, PRKD1, RAC1, RICTOR, EIF1AX, NRIP1, CHD3, NRG3, CARD10, CNOT3, NUP98, NUMB, CHD6, CNTFR, CSF1, CTSL, CRTC1, CRTC3, CSNK1E, COPS3, CTSS, CSK, CREM, CREB3L4, CTCFL, CRTC2, PAK1, PARP4, DCUN1D1, DDX6, PATZ1, DDR1, PDGFC, PARP2, PAK4, PAK6, DIS3, PCBP1, CYP2J2, PAXIP1, PBX2, DDX5, DIRAS3, PDCD1, PBRM1, DDIT3, DAXX, CYP2C8, DCUN1D2, PDGFD, PDCD1LG2, EPHB1, ELK4, ELF5, E2F6, EPHA3, E2F7, EBF1, DOT1L, EPHA1, ELF1, ELK3, DYRK2, PEG3, EPHB6, EHF, EPHA5, PHF2, EHMT2, EPHA8, EPHA4, DMXL1, EPGN, EPHB3, PDS5B, DNMT3L, ECT2L, ELF4, PARP1, SETD1A, KDM5A, CNKSR1, KDM6B, TRAF3IP1, CTNND1, DVL3, EED, TBX22, NKX2-6, ERBB4, JMJD1C, PPP2R1A, HDAC6, KAT2B, KMT5B, ASH1L, TRIO, MAP3K7, CIC, MAPK8, TET1, CHD4, BRDT, CBX2, PRLR, BCL11A, SMARCD2, KDM1A, AXL, PRDM13, NRTN, NONO, PRDM12, WNT4, ROR2, DNMT3B, DHH, HOXA13, ESCO2, CCND2, ZNF423, ZBTB20, MNX1, NKX2-2, IL2RA, NFIA, WNT5A, NTRK2, PRMT7, SAMD9, CARD11, POT1, TRAF3, EPOR, NOTCH2, TYK2, PRKDC, IL10RB, ICOS, PIK3R1, VKORC1, IL10RA, CTLA4, ABCC2, NFKB2, STK4, IL12RB1, CIITA, AIP, FADD, NFKBIA, PIK3CD, BCR, PTPRC, STAT5B, RAC2, GFI1, G6PC3, ITK, FASLG, XIAP, ELANE, FAS, EXT1, EXT2, AKT1, AKT3, PIK3R2, INSR, GNA11, AXIN2, POLE, ABRAXAS1, ZAP70, IL7R, CD40LG, CD40, CBLC, BCORL1, CBLB, CSF3R, CUX1, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, EGFR, TPMT, NPM1, FLT3, RARB, GFI1B, HOXA11, TBXAS1, GNAQ, GGCX, GATA6, GLIS3, BLK, PAX4, AKT2, ABCA1, ABCG1, GREM1, POLD1, APOB, PCSK9, APOA1, ACVR2B, SLC6A3, DRD2, HMGCR, CSF1R, IL11RA, MYCN, PIK3CA, GLIS2, NEK8, USB1, THPO, ERCC4, VEGFA, DIAPH2, TLR1, BDNF, SLC6A4, STK3, CDKN1B, BAP1, XRCC2, CYP2D6, FANCD2, FANCI, FANCL, FANCM, SLX4, CYP2C19, FANCE, FANCF, FANCG, FANCA, KITLG, NOD2, SMAD2, CREB3L1, WNT1, NR3C2, GNAS, NOP10, NHP2, DBH, CALR, MGMT, SH2B3, JAK3, ASXL1, KIT, EP300, ACE, MBD1, MBD3, WNK3, PRSS1, FGF10, SH2D1A, FLT4, TEK, VEGFC, NT5C2, SMARCA2, ARID1A, SMARCB1, SMARCA4, KMT2A, HELLS, SMARCE1, ARID2, ERBB3, RIPK4, NEK9, NEK2, MYL3, MYL2, DSC2, TNNT2, TPM1, JUP, DSG2, PRKAG2, TNNI3, NKX2-5, PRDM16, ACTC1, NKX2-1, CSF2RB, CSF2RA, SMAD9, TERT, BMPR1B, TERC, MAF, CDH3, CTNNA1, TFG, KDM6A, TP63, AKAP9, KCNJ5, RYR2, MITF, PKP2, CACNB2, GLI3, EZH2, NFIX, DNMT3A, ACVR1, PRDM5, MYH11, ACTA2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, ATR, GLI2, ABCB1, MTOR, SPRED1, SOX9, TWIST1, POR, RAB23, CDK16, ZMYM3, KLF8, SOX3, TAF1, BRWD3, RBM10, USP9X, DKC1, FANCB, AFF2, PHF8, FOXP3, RASA1, RPL5, GATA1, KAT6B, FAT4, LZTR1, CTNNB1, ARID1B, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, DIAPH3, ROR1, GATA3, FGF3, CDC14A, PTPRQ, KCNQ1, SOX10, PAX3, DNMT1, DIAPH1, ERCC3, ERCC2, HGF, ZEB2, PICALM, ROBO2, IL17RA, TRAF3IP2, DEK, MSH3, PML, AURKC, MAFB, SOX17, EGF, PALLD, CTNNA2, RNF213, DDR2, MDM2, WNT10B, IGF1R, ETV5, MLH3, FBXW11, MALT1, SMAD6, IL21R, NFKB1, ABL2, DUSP22, DDB2, MTAP, CEBPE, ARID5B, PRPF40B, CDK12, TBX3, HDAC4, BCL2, SLC26A3, CCND1, IGF1, NR3C1, TWIST2, TMC8, CYP1A2, TMC6, FGF9, HR, XPC, RBPJ, MAP3K3, CDK19, HOXA3, GRB10, KAT6A, DDX3X, HOXB13, DHFR, KEL, HLA-B, HOXD10, NGF, CYP2C9, CD79B, CD79A, BLNK, VAV1, SLCO1B3, SLCO1B1, LIFR, WNK4, CUL3, GDNF, ASCL1, B2M, KDSR, GATA5, PLCG2, HTR1A, CARD8, PSENEN, LYN, NCSTN, TNFAIP3, ZNF384, WNT10A, KDR, FLT1, NLRP1, FLG, CTNNA3, CYLD, ALOX12B, NKX3-2, HOXD13, NSD2, GALNT12, BUB1B, RAD51, PRDM8, XPA, MAPK10, FGF12, ERCC5, CAMTA1, KMT2B, PDGFB, PDGFRB, DICER1, CDH7, CYP2R1, PAX8, ASXL3, PLAGL1, WRN, PLK4, CDC6, TCF12, ERF, CRBN, CTCF, CLIP1, SETD5, ZMYND11, CDK6, CENPE, FLI1, RUNX1T1, SRC, CDK5, FGF17, MAMLD1, FSHR, NEK1, ICK, IRF6, MAP3K1, WNT7A, SETBP1, CUL4B, KDM5C, PAK3, PHF6, ATRX, TCF4, TBL1XR1, SETD2, MAGI2, KMT2D, SCN5A, GRIN2A, CHD2, KCNH2, MCPH1, FGF14, MUSK, SMCHD1, TMEM43, SYNE1, MYBPC3, FUS, RYR1, CACNA1S, PDK1, MYH7, FGF23, GHR, CYP21A2, HSD11B2, FGF8, GNRHR, LHCGR, FGFR1, NR0B1, LRRK2, NF1, TBP, PPP2R2B, NOTCH3, PSEN2, WNK1, NTRK1, LMNA, DNM2, EGR2, NDRG1, DPYD, PKHD1, BTK, WAS, MPL, UGT1A1, G6PD, RAD51D, PMS1, BARD1, RAD51C, CDC73, PRKAR1A, PRF1, CEBPA, SBDS, PAX5, GATA2, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, GPC3, MET, FLCN, SDHD, CDKN1C, CDKN2A, CDK4, STK11, CDH1, SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, MRE11, ATM, ALK, NSD1, NIPBL, TSC1, SMC1A, SMC3, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, VDR, TINF2, SOS1, SHOC2, RUNX2, PTPN11, NRAS, MAP2K1, LEPR, LDLR, KRAS, HRAS, GLA, FOXG1, CREBBP, CHD7, BRAF, BLM, FANCC, ELP1, ARX, AR, FGFR3, TSHR, IL2RG, SDHA, MAK, TEAD1, PHB, PLA2G2A, PAX2, MEN1, STAT3, TMEM127, ZFHX3, NCOA4, CYP17A1, SOX2, PPP2R1B, PRKN, BCOR, AMER1, MAOA, PHOX2A, CTSD, HAX1, SDHB, IDH2, MERTK, PRPF6, GOT1, CHD1L, CD70, MAD2L2, MAP3K8, PRRX1, NUP93, FAT1, TNK2, GPC5, RXRA, CYP4F2, CYP2A6, TBX18, DVL1, RNF43, DCC, OSMR, HOXC13, IHH, IGF2R, CDKN2C, CKS1B, MECOM, RPN1, BIRC3, MYC, BCL6, LRP6, SMO, YWHAE, PTCH2, FGF20, PTPRF, CDKN2B, MLLT1, EPHA2, MLLT3, NAT2, MN1, ADRB2, NUP214, CYP3A4, AFF3, TAL1, ZBTB16, PBX1, TCF3, RARA, ERCC1, PAX9, CBFB, ERBB2, WNT3, FBN1, FH, RAF1, SDHC, KIF1B, DSP, SHH, COMT, CASP8, MC1R, RET, HNF1B, SDHAF2, PSEN1, RB1, TLR4, TGFB1, PAX6, WT1, STAT1, COL3A1, LRP5, PPARG, HNF1A, FOXL2, FKBP10, ABCB4, ABCB11, TP53, RUNX1, RECQL4, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1 Specificity 1 % Genes 28 %
COL1A1/2 Related Disorders Panel (MitomeNGS). By Baylor Miraca Genetics Laboratories in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
PreSeek Non-invasive Prenatal Gene Sequencing Screen. By Baylor Miraca Genetics Laboratories in United States. NSD1, NIPBL, TSC1, SMC1A, SMC3, SYNGAP1, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...) View the complete list with 10 more genes Panel GTR000552480 complete gene list NSD1, NIPBL, TSC1, SMC1A, SMC3, SYNGAP1, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, CHD7, CDKL5, BRAF, FGFR3, MECP2, RAF1, JAG1, COL1A2, COL1A1 Specificity 7 % Genes 19 %
Osteogenesis Imperfecta Evaluation. By Athena Diagnostics Inc in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
COL1A1 (OI) DNA Sequencing Test. By Athena Diagnostics Inc in United States. COL1A1 Specificity 100 % Genes 10 %
NGS Skeletal Dysplasia Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States. SOX9, COMP, FLNA, HSPG2, TRPV4, SLC26A2, FGFR3, COL1A2, COL1A1, COL2A1 Specificity 20 % Genes 19 %
NGS Aortic Dysfunction or Dilation and Related Disorders Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States. MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, PLOD1, COL5A2, COL5A1, CBS, FBN1, ELN, COL3A1, COL1A1, FBLN5 Specificity 5 % Genes 10 %
NGS Connective Tissue Disorders Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States. ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A1, PKD2 , (...) View the complete list with 15 more genes Panel GTR000525132 complete gene list ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ATP6V0A2, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5, ATP7A Specificity 6 % Genes 19 %
Osteogenesis Imperfecta. By Center for Human Genetics, Inc in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Connective Tissue Disorders 22-gene panel. By Center for Human Genetics, Inc in United States. NTM, TGFBR3, PRKG1, MYH11, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A2, COL11A1, FLNA, COL5A2, COL5A1, FBN1, COL3A1, COL1A2 , (...) View the complete list with 2 more genes Panel GTR000529183 complete gene list NTM, TGFBR3, PRKG1, MYH11, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A2, COL11A1, FLNA, COL5A2, COL5A1, FBN1, COL3A1, COL1A2, COL1A1, COL2A1 Specificity 10 % Genes 19 %
COL1A1/COL1A2-Related Osteogenesis Imperfecta genomic sequencing and deletion/duplication analysis. By Collagen Diagnostic Laboratory University of Washington in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Caffey disease. By Collagen Diagnostic Laboratory University of Washington in United States. COL1A1 Specificity 100 % Genes 10 %
Autosomal Dominant Osteogenesis imperfecta panel. By Collagen Diagnostic Laboratory University of Washington in United States. COL1A2, COL1A1, IFITM5 Specificity 67 % Genes 19 %
Ehlers-Danlos type VII (EDS VII) genomic sequencing and deletion/duplication analysis. By Collagen Diagnostic Laboratory University of Washington in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Comprehensive Ehlers-Danlos Syndrome Panel. By Collagen Diagnostic Laboratory University of Washington in United States. C1R, C1S, CHST14, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, ATP7A Specificity 16 % Genes 19 %
Connective Tissue Disorders Panel. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States. B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA , (...) View the complete list with 11 more genes Panel GTR000552207 complete gene list B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 7 % Genes 19 %
Familial Aneurysm and Aortopathy. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States. B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA , (...) View the complete list with 11 more genes Panel GTR000552215 complete gene list B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 7 % Genes 19 %
COL1A1 Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States. COL1A1 Specificity 100 % Genes 10 %
COL1A1. By Institute for Human Genetics University Clinic Freiburg in Germany. COL1A1 Specificity 100 % Genes 10 %
Connective Tissue Disorders Panel. By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States. ADAMTS10, SMAD2, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1 , (...) View the complete list with 30 more genes Panel GTR000327667 complete gene list ADAMTS10, SMAD2, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, ADAMTSL2, MED12, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, FLNA, PKD2, ADAMTS2, SMAD4, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, ALDH18A1, FBN1, ATP6V0A2, PYCR1, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5, ATP7A Specificity 4 % Genes 19 %
Ehlers-Danlos Syndrome, Arthrochalasia Type. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis Imperfecta, autosomal dominant. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. COL1A2, COL1A1 Specificity 100 % Genes 19 %
COL2A1, FGFR3, SLC26A2, COL1A2, COL1A1, CRTAP, SOX9, ALPL, LEPRE1. NextGeneDx.Complete sequencing by NGS. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. SOX9, SLC26A2, FGFR3, CRTAP, COL1A2, COL1A1, COL2A1, ALPL Specificity 38 % Genes 28 %
COL1A1, COL1A2. NextGeneDx.Complete sequencing by NGS. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
COL1A1. MLPA testing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A1 Specificity 100 % Genes 10 %
COL1A1, COL1A2. MLPA testing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
COL1A1, COL1A2, CRTAP, LEPRE1. NextGeneDx.Complete sequencing by NGS. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. CRTAP, COL1A2, COL1A1 Specificity 100 % Genes 28 %
COL1A1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta Seq + Del/Dup Panel. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Connective Tissue Seq Analysis. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...) View the complete list with 15 more genes Panel GTR000553469 complete gene list SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, COL4A5, SMAD4, PLOD1, COL5A2, COL5A1, CBS, PLOD3, FBN1, COL3A1, COL1A2, COL1A1, FBLN5 Specificity 6 % Genes 19 %
Connective Tissue Seq + Del/Dup Panel. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...) View the complete list with 16 more genes Panel GTR000553480 complete gene list SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, COL4A5, SMAD4, PLOD1, COL5A2, COL5A1, CBS, PLOD3, FBN1, ELN, COL3A1, COL1A2, COL1A1, FBLN5 Specificity 6 % Genes 19 %
Connective Tissue Del/Dup Panel. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...) View the complete list with 16 more genes Panel GTR000553483 complete gene list SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, COL4A5, SMAD4, PLOD1, COL5A2, COL5A1, CBS, PLOD3, FBN1, ELN, COL3A1, COL1A2, COL1A1, FBLN5 Specificity 6 % Genes 19 %
Osteogenesis Imperfecta Seq Analysis. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis Imperfecta Del/Dep Panel. By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis imperfecta type 1, 2, 3, 4 (sequence analysis of COL1A1 and COL1A2 genes). By CGC Genetics in Portugal. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis Imperfecta (sequence analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome type 1 (sequence analysis of COL1A1 and COL1A2 genes). By CGC Genetics in Portugal. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers-Danlos syndrome type VII (sequence analysis of COL1A1 and COL1A2 genes). By CGC Genetics in Portugal. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis imperfecta (deletion/duplication analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome (NGS panel for 12 genes). By CGC Genetics in Portugal. CHST14, TNXB, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 17 % Genes 19 %
Skeletal dysplasia (NGS panel for 31 genes). By CGC Genetics in Portugal. MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2 , (...) View the complete list with 11 more genes Panel GTR000523894 complete gene list MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, CRTAP, P3H1, COL1A2, COL1A1, COL2A1, ALPL Specificity 13 % Genes 37 %
Ehlers-Danlos syndrome (deletion/duplication analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Caffey disease (sequence analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome (deletion/duplication analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Caffey disease (sequence analysis of COL1A1 gene). By CGC Genetics in Portugal. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndromes Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics in United States. ATP6V1E1, AEBP1, ATP6V1A, LZTS1, ATP6AP1, FLNB, DSE, CHST3, RIN2, TNFRSF1A, GGCX, B3GALT6, C1R, C1S, GORAB, B3GAT3, SPARC, COL12A1, EFEMP2, ZNF469 , (...) View the complete list with 25 more genes Panel GTR000514879 complete gene list ATP6V1E1, AEBP1, ATP6V1A, LZTS1, ATP6AP1, FLNB, DSE, CHST3, RIN2, TNFRSF1A, GGCX, B3GALT6, C1R, C1S, GORAB, B3GAT3, SPARC, COL12A1, EFEMP2, ZNF469, CHST14, TNXB, PRDM5, FKBP14, TGFBR2, TGFBR1, SMAD3, ADAMTSL2, FLNA, ADAMTS2, PLP1, PLOD1, COL5A2, COL5A1, SLC39A13, ALDH18A1, ATP6V0A2, PYCR1, ELN, COL3A1, COL1A2, COL1A1, FBLN5, B4GALT7, ATP7A Specificity 5 % Genes 19 %
Osteogenesis Imperfecta via the COL1A1 Gene. By PreventionGenetics PreventionGenetics in United States. COL1A1 Specificity 100 % Genes 10 %
Dense bone dysplasia NGS panel. By Connective Tissue Gene Tests in United States. SLCO2A1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, GJA1, TNFRSF11B, TGFB1, SOST, COL1A1, TYROBP, ANKH Specificity 8 % Genes 10 %
Ehlers-Danlos syndrome NGS panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. DSE, B3GALT6, C1R, C1S, COL12A1, ZNF469, CHST14, PRDM5, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7, ATP7A Specificity 10 % Genes 19 %
Ehlers-Danlos syndrome Comprehensive panel - Dominant. By Connective Tissue Gene Tests in United States. C1R, C1S, COL12A1, FLNA, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 23 % Genes 19 %
Ehlers-Danlos syndrome NGS panel - Dominant. By Connective Tissue Gene Tests in United States. C1R, C1S, COL12A1, FLNA, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 23 % Genes 19 %
Ehlers-Danlos syndrome Deletion / Duplication panel - Dominant. By Connective Tissue Gene Tests in United States. C1R, C1S, COL12A1, FLNA, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 23 % Genes 19 %
Ehlers-Danlos syndrome Deletion / Duplication panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. DSE, B3GALT6, C1R, C1S, COL12A1, ZNF469, CHST14, PRDM5, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7, ATP7A Specificity 10 % Genes 19 %
Dense bone dysplasia Comprehensive panel. By Connective Tissue Gene Tests in United States. SLCO2A1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, GJA1, TNFRSF11B, TGFB1, SOST, COL1A1, TYROBP, ANKH Specificity 8 % Genes 10 %
Dense bone dysplasia Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. SLCO2A1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, GJA1, TNFRSF11B, TGFB1, SOST, COL1A1, TYROBP, ANKH Specificity 8 % Genes 10 %
Ehlers-Danlos syndrome Comprehensive panel - Dominant & Recessive. By Connective Tissue Gene Tests in United States. DSE, B3GALT6, C1R, C1S, COL12A1, ZNF469, CHST14, PRDM5, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7, ATP7A Specificity 10 % Genes 19 %
Osteogenesis imperfecta COL1A1 & COL1A2 Comprehensive panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis imperfecta COL1A1 & COL1A2 NGS panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis imperfecta COL1A1 & COL1A2 Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Skeletal dysplasia core & extended Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2 , (...) View the complete list with 9 more genes Panel GTR000559336 complete gene list MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 7 % Genes 19 %
Osteogenesis imperfecta Comprehensive panel - Dominant. By Connective Tissue Gene Tests in United States. P4HB, PLS3, ANO5, COL1A2, COL1A1, IFITM5, ALPL Specificity 29 % Genes 19 %
Osteogenesis imperfecta core Comprehensive panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1, IFITM5 Specificity 67 % Genes 19 %
Skeletal dysplasia core & extended Comprehensive panel. By Connective Tissue Gene Tests in United States. MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2 , (...) View the complete list with 9 more genes Panel GTR000559351 complete gene list MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 7 % Genes 19 %
Skeletal dysplasia core Comprehensive panel. By Connective Tissue Gene Tests in United States. INPPL1, TRIP11, NKX3-2, SOX9, SLC26A2, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 20 % Genes 19 %
Skeletal dysplasia core NGS panel. By Connective Tissue Gene Tests in United States. INPPL1, TRIP11, NKX3-2, SOX9, SLC26A2, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 20 % Genes 19 %
Osteogenesis imperfecta core Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1, IFITM5 Specificity 67 % Genes 19 %
Osteopetrosis and Dense bone dysplasia Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7 , (...) View the complete list with 8 more genes Panel GTR000559382 complete gene list SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, TYROBP, ANKH Specificity 4 % Genes 10 %
Skeletal dysplasia core & extended NGS panel. By Connective Tissue Gene Tests in United States. MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2 , (...) View the complete list with 9 more genes Panel GTR000559386 complete gene list MMP9, INPPL1, MMP13, DDR2, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, ARSE, SOX9, NSDHL, EBP, PTH1R, COL11A2, COL11A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 7 % Genes 19 %
Osteogenesis imperfecta Deletion / Duplication panel - Dominant. By Connective Tissue Gene Tests in United States. P4HB, PLS3, ANO5, COL1A2, COL1A1, IFITM5, ALPL Specificity 29 % Genes 19 %
Osteopetrosis and Dense bone dysplasia NGS panel. By Connective Tissue Gene Tests in United States. SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7 , (...) View the complete list with 8 more genes Panel GTR000559412 complete gene list SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, TYROBP, ANKH Specificity 4 % Genes 10 %
Osteogenesis imperfecta NGS panel - Dominant. By Connective Tissue Gene Tests in United States. P4HB, PLS3, ANO5, COL1A2, COL1A1, IFITM5, ALPL Specificity 29 % Genes 19 %
Osteopetrosis and Dense bone dysplasia Comprehensive panel. By Connective Tissue Gene Tests in United States. SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7 , (...) View the complete list with 8 more genes Panel GTR000559422 complete gene list SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, FERMT3, GJA1, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, TYROBP, ANKH Specificity 4 % Genes 10 %
Skeletal dysplasia core Deletion / Duplication panel. By Connective Tissue Gene Tests in United States. INPPL1, TRIP11, NKX3-2, SOX9, SLC26A2, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 20 % Genes 19 %
Osteogenesis imperfecta core NGS panel. By Connective Tissue Gene Tests in United States. COL1A2, COL1A1, IFITM5 Specificity 67 % Genes 19 %
Osteogenesis imperfecta, types I, II, III & IV Comprehensive Test A. By Connective Tissue Gene Tests in United States. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, types I, II, III & IV NGS Test A. By Connective Tissue Gene Tests in United States. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, types I, II, III & IV Deletion / Duplication Test A. By Connective Tissue Gene Tests in United States. COL1A1 Specificity 100 % Genes 10 %
COL1A1/2-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. COL1A1 Specificity 100 % Genes 10 %
Marfan syndrome, EDS and other connective tissue disorders - different panels. By Institute of Human Genetics Cologne University in Germany. GATA5, DSE, B3GALT6, MAT2A, MFAP5, PRKG1, TGFB3, EFEMP2, CHST14, TNXB, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3 , (...) View the complete list with 17 more genes Panel GTR000558417 complete gene list GATA5, DSE, B3GALT6, MAT2A, MFAP5, PRKG1, TGFB3, EFEMP2, CHST14, TNXB, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, COL4A5, ADAMTS2, SMAD4, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ELN, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 6 % Genes 19 %
Ehlers-Danlos Syndrome (EDS). By MGZ Medical Genetics Center in Germany. ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 15 % Genes 19 %
Vascular and connective tissue diseases - panels. By MGZ Medical Genetics Center in Germany. JAM3, AIMP1, CST3, COL4A2, ADAMTSL4, ADA2, MAT2A, MFAP5, PRKG1, ADAR, ADCY6, TGFB3, BMPR2, EFEMP2, SMAD9, CAV1, KCNK3, BMPR1B, ACVRL1, ZNF469 , (...) View the complete list with 47 more genes Panel GTR000552434 complete gene list JAM3, AIMP1, CST3, COL4A2, ADAMTSL4, ADA2, MAT2A, MFAP5, PRKG1, ADAR, ADCY6, TGFB3, BMPR2, EFEMP2, SMAD9, CAV1, KCNK3, BMPR1B, ACVRL1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, AFF2, AGTR2, CACNA1C, HTRA1, TREX1, FLNA, COL4A1, AGRN, NOTCH3, ADAMTS2, ENG, PLOD1, GLA, COL5A2, COL5A1, CBS, AIFM1, OTC, COQ8A, SLC39A13, AGK, FBN1, AFG3L2, POLG, AMACR, COL3A1, COL1A2, COL1A1, ADSL, B4GALT7, AGL, TTR Specificity 3 % Genes 19 %
Caffey Disease. By Bioscientia GmbH Center for Human Genetics in Germany. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndrome Type VIIA. By Bioscientia GmbH Center for Human Genetics in Germany. COL1A1 Specificity 100 % Genes 10 %
COL1A1/2-Related Osteogenesis Imperfecta. By Bioscientia GmbH Center for Human Genetics in Germany. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers Danlos syndrome. By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany. PLOD1, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 34 % Genes 19 %
Osteogenesis Imperfecta. By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers-Danlos syndrome type VIIA. By Centogene AG - the Rare Disease Company in Germany. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta. By Centogene AG - the Rare Disease Company in Germany. COL1A1 Specificity 100 % Genes 10 %
CentoICU platinum plus. By Centogene AG - the Rare Disease Company in Germany. OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN , (...) View the complete list with 494 more genes Panel GTR000530427 complete gene list OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN, IGF1R, MALT1, IL21R, PCK1, IGF1, HGD, UMPS, TRHR, SLC52A1, SERPINC1, PEPD, GP9, ACTN1, ASNS, FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4, PROS1, LRBA, PIK3CD, C15orf41, GSS, EPB42, ANK1, SPTA1, SPTB, PTPRC, LIG4, NHEJ1, RAC2, LAMTOR2, RBM8A, ELANE, SLC4A1, INSR, GNA11, ZAP70, RAG1, RAG2, IL7R, CD3D, CD3E, CD40LG, CD40, AICDA, TNFRSF13B, MASTL, ITGA2B, ITGB3, GFI1B, STIM1, P2RY12, P2RX1, FGG, FGB, FGA, GP1BA, EIF2AK3, PTF1A, GLIS3, AKT2, APOC2, HADH, PSPH, PCBD1, DDC, MAT1A, SLC46A1, MYCN, RBBP8, IER3IP1, RAB18, EVC2, EVC, AKR1D1, BDNF, FANCD2, FANCA, ADAMTS13, F8, F9, GNAS, JAK3, TBX5, SALL4, CD320, LHX3, LHX4, TBX19, SPINK1, F11, RAB3GAP2, DNA2, PRKAG2, SFTPB, SFTPC, ABCA3, DOCK8, SFTPD, KDM6A, AKAP9, CALM1, MITF, GPSM2, CACNB2, ATR, PCNT, CDK5RAP2, CEP152, SPRED1, COMP, NAA10, RPS6KA3, FANCB, MAGT1, CDAN1, NEU1, UROS, PKLR, MVK, KLF1, GATA1, GATA3, SIX1, KCNQ1, KCNE1, PRPS1, SIX5, KCNQ4, PAX3, PNPT1, COL11A1, EDN3, CACNA1D, ATP6V1B1, SALL1, ZEB2, CASK, ATRX, TCF4, KCNJ10, SPTAN1, KMT2D, STIL, RAB3GAP1, CENPJ, BCKDK, EPM2A, PNPO, KCNQ3, KCNQ2, SCN2A, ST3GAL5, KCNH2, NHLRC1, ASPM, MCPH1, LAMA2, POMT1, POMT2, PLEC, PKD2, BSND, POU1F1, HNF4A, PDX1, INS, CASR, KCNJ11, NR0B1, GCH1, SCN1A, CSTB, WNK1, EGR2, PMP22, TGM1, PKHD1, PHGDH, LAMC2, BTK, ABCC8, WAS, SUMF1, LAMA3, UGT1A1, SLC26A2, SLC7A7, SERPINA1, DCLRE1C, PROP1, CTNS, G6PD, FKTN, LAMB3, SBDS, GPC3, PHOX2B, NSD1, NIPBL, TSC1, TSC2, MAP2K2, FGFR2, WDR62, SOS1, SLC2A1, SHOC2, RPS19, RMRP, NRAS, NPC2, NPC1, MEF2C, MAP2K1, LIPA, KRAS, HRAS, GLA, GJB2, FOXG1, DHCR7, CHD7, CDKL5, BRAF, F13A1, CD79B, IGLL1, CD79A, BLNK, LRRC8A, SLCO1B3, SLCO1B1, PSAT1, LIPN, CYP4F22, PNPLA1, ALOXE3, STS, CERS3, NIPAL4, ALOX12B, SERPING1, F10, PET100, COA5, SERAC1, TG, TPO, SLC5A5, DUOX2, DUOXA2, THRA, TSHB, PAX8, SLC25A1, CACNA1C, FUCA1, TJP2, FANCC, CFTR, ASPA, ARSA, TSHR, PNP, IL2RG, HPD, GNMT, DOLK, SUGCT, ARSB, AHCY, AGA, ADA, ABCD4, PDHX, PAX2, HESX1, ANKRD26, CYP17A1, OGDH, ALMS1, SOX2, ASL, PMM2, SLC25A20, SLC22A5, ASS1, SLC3A1, LRPPRC, GLYCTK, GALK1, GALE, GALT, GCDH, ETFDH, ETFA, ETFB, GBE1, CBS, NAGS, IVD, OXCT1, GALC, DLAT, SUCLG1, MLYCD, MAN2B1, DBT, HIBCH, MUT, MMAA, MMAB, NDUFAF5, NDUFS2, NDUFV2, NDUFA11, SDHAF1, MOCS1, MOCS2, GALNS, GUSB, CPT1A, NDUFAF6, NDUFS7, COX15, NDUFA2, CTSA, OAT, AGXT, ACOX1, ALDH7A1, HEXB, ALDH3A2, ALDH5A1, SUOX, HEXA, TCN2, LMBRD1, MMADHC, SLC9A6, AIFM1, TAZ, GK, PDHA1, OTC, D2HGDH, ETHE1, AMT, GLDC, HMGCS2, PCCA, COQ2, UCP2, UNG, PDP1, HADHB, ACADSB, CTSD, DNAJC19, CRTAP, P3H1, ACAD8, SUCLA2, STXBP1, SPR, GATM, GAMT, ABAT, TAT, HSD3B2, HMGCL, NDUFAF1, FAH, NFU1, ALDH6A1, PDHB, ACSF3, LIAS, PDSS1, PDSS2, COQ9, FBN1, CYP11B2, MECP2, SMPD1, FH, OPA3, RAF1, HADHA, SLC25A13, ALAS2, NDUFAF2, FOXRED1, CYP11B1, GCK, SLC25A19, NDUFS4, POLG, DLD, AASS, CEP290, ADGRV1, MKKS, HPRT1, JAG1, HSD17B10, GNE, PRODH, GLB1, GNPTAB, PSAP, COMT, PTPN11, POMC, PLOD1, PAH, QDPR, PTS, WFS1, TRMU, KRT5, CPT2, CPS1, HSD17B4, MTRR, SLC16A1, ABCA12, EYA4, SLC37A4, RET, MTR, HNF1B, PSEN1, RB1, WT1, STAR, COL1A2, COL1A1, EYA1, MMACHC, HBB, HNF1A, ADSL, GAA, C12orf65, BCS1L, BCKDHB, BCKDHA, AUH, ATP8B1, ATP7B, BTD, ATP7A, HLCS, ARG1, ALPL, GYS2, PC, FBP1, ALDOB, ALDOA, ACAT1, ACADVL, AGL, ACADS, ACADM, ACADL, ACAD9, AARS2, MCCC2, MCCC1, UBE3A, MTHFR, F5, F2, BRCA2 Specificity 1 % Genes 37 %
CentoICU platinum. By Centogene AG - the Rare Disease Company in Germany. FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4 , (...) View the complete list with 494 more genes Panel GTR000530428 complete gene list FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4, PROS1, LRBA, PIK3CD, C15orf41, GSS, EPB42, ANK1, SPTA1, SPTB, PTPRC, LIG4, NHEJ1, RAC2, LAMTOR2, RBM8A, ELANE, SLC4A1, INSR, GNA11, ZAP70, RAG1, RAG2, IL7R, CD3D, CD3E, CD40LG, CD40, AICDA, TNFRSF13B, MASTL, ITGA2B, ITGB3, GFI1B, STIM1, P2RY12, P2RX1, FGG, FGB, FGA, GP1BA, EIF2AK3, PTF1A, GLIS3, AKT2, APOC2, HADH, PSPH, PCBD1, DDC, MAT1A, SLC46A1, MYCN, RBBP8, IER3IP1, RAB18, EVC2, EVC, AKR1D1, BDNF, FANCD2, FANCA, ADAMTS13, F8, F9, GNAS, JAK3, TBX5, SALL4, CD320, LHX3, LHX4, TBX19, SPINK1, F11, RAB3GAP2, DNA2, PRKAG2, SFTPB, SFTPC, ABCA3, DOCK8, SFTPD, KDM6A, AKAP9, CALM1, MITF, GPSM2, CACNB2, ATR, PCNT, CDK5RAP2, CEP152, SPRED1, COMP, NAA10, RPS6KA3, FANCB, MAGT1, CDAN1, NEU1, UROS, PKLR, MVK, KLF1, GATA1, CACNA1C, FUCA1, TJP2, GATA3, SIX1, KCNQ1, KCNE1, PRPS1, SIX5, KCNQ4, PAX3, PNPT1, COL11A1, EDN3, CACNA1D, ATP6V1B1, SALL1, ZEB2, CASK, ATRX, TCF4, KCNJ10, SPTAN1, KMT2D, STIL, RAB3GAP1, CENPJ, BCKDK, EPM2A, EGR2, PMP22, TGM1, PKHD1, PHGDH, LAMC2, BTK, ABCC8, WAS, SUMF1, LAMA3, UGT1A1, SLC26A2, SLC7A7, SERPINA1, DCLRE1C, PROP1, CTNS, G6PD, FKTN, LAMB3, SBDS, GPC3, PHOX2B, NSD1, NIPBL, TSC1, TSC2, MAP2K2, FGFR2, WDR62, SOS1, SLC2A1, SHOC2, RPS19, RMRP, PTPN11, POMC, PLOD1, NRAS, NPC2, NPC1, MEF2C, MAP2K1, LIPA, KRAS, HRAS, GLA, GJB2, FOXG1, DHCR7, CHD7, CDKL5, BRAF, FANCC, CFTR, ASPA, ARSA, TSHR, PNP, IL2RG, HPD, GNMT, DOLK, SUGCT, ARSB, AHCY, AGA, ADA, ABCD4, PDHX, PAX2, OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN, IGF1R, MALT1, IL21R, PCK1, IGF1, HGD, UMPS, TRHR, SLC52A1, SERPINC1, PEPD, F13A1, CD79B, IGLL1, CD79A, BLNK, LRRC8A, SLCO1B3, SLCO1B1, PSAT1, LIPN, CYP4F22, PNPLA1, ALOXE3, STS, CERS3, NIPAL4, ALOX12B, SERPING1, F10, PET100, COA5, SERAC1, TG, TPO, SLC5A5, DUOX2, DUOXA2, THRA, TSHB, PAX8, SLC25A1, GP9, ACTN1, ASNS, HESX1, ANKRD26, CYP17A1, OGDH, ALMS1, SOX2, ASL, PMM2, SLC25A20, SLC22A5, ASS1, SLC3A1, LRPPRC, GLYCTK, GALK1, GALE, GALT, GCDH, ETFDH, ETFA, ETFB, GBE1, CBS, NAGS, IVD, OXCT1, GALC, DLAT, SUCLG1, MLYCD, MAN2B1, DBT, HIBCH, MUT, MMAA, MMAB, NDUFAF5, NDUFS2, NDUFV2, NDUFA11, SDHAF1, MOCS1, MOCS2, GALNS, GUSB, CPT1A, NDUFAF6, NDUFS7, COX15, NDUFA2, CTSA, OAT, AGXT, PAH, QDPR, PTS, ACOX1, ALDH7A1, HEXB, ALDH3A2, ALDH5A1, SUOX, HEXA, TCN2, LMBRD1, MMADHC, SLC9A6, AIFM1, TAZ, GK, PDHA1, OTC, D2HGDH, ETHE1, AMT, GLDC, HMGCS2, PCCA, COQ2, UCP2, UNG, PDP1, HADHB, ACADSB, CTSD, DNAJC19, CRTAP, P3H1, ACAD8, SUCLA2, STXBP1, SPR, GATM, GAMT, ABAT, TAT, HSD3B2, HMGCL, NDUFAF1, FAH, NFU1, ALDH6A1, PDHB, ACSF3, LIAS, PDSS1, PDSS2, COQ9, FBN1, CYP11B2, MECP2, SMPD1, FH, OPA3, RAF1, HADHA, SLC25A13, ALAS2, NDUFAF2, FOXRED1, CYP11B1, GCK, SLC25A19, NDUFS4, POLG, DLD, AASS, CEP290, ADGRV1, MKKS, HPRT1, JAG1, HSD17B10, GNE, PRODH, GLB1, GNPTAB, PSAP, COMT, WFS1, TRMU, KRT5, CPT2, CPS1, HSD17B4, MTRR, SLC16A1, ABCA12, EYA4, SLC37A4, RET, MTR, HNF1B, PSEN1, PNPO, KCNQ3, KCNQ2, SCN2A, ST3GAL5, KCNH2, NHLRC1, ASPM, MCPH1, LAMA2, POMT1, POMT2, PLEC, PKD2, BSND, POU1F1, HNF4A, PDX1, INS, CASR, KCNJ11, NR0B1, GCH1, SCN1A, CSTB, WNK1, RB1, WT1, STAR, COL1A2, COL1A1, EYA1, MMACHC, HBB, HNF1A, ADSL, GAA, C12orf65, BCS1L, BCKDHB, BCKDHA, AUH, ATP8B1, ATP7B, BTD, ATP7A, HLCS, ARG1, ALPL, GYS2, PC, FBP1, ALDOB, ALDOA, ACAT1, ACADVL, AGL, ACADS, ACADM, ACADL, ACAD9, AARS2, MCCC2, MCCC1, UBE3A, MTHFR, F5, F2, BRCA2 Specificity 1 % Genes 37 %
COL1A1/2-Related Osteogenesis Imperfecta. By bio.logis Center for Human Genetics Diagnosticum in Germany. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers-Danlos Syndrome Type VIIA. By bio.logis Center for Human Genetics Diagnosticum in Germany. COL1A1 Specificity 100 % Genes 10 %
Connective tissue disorders - Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, Aortic Aneurysm. By CeGaT GmbH in Germany. DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...) View the complete list with 24 more genes Panel GTR000522392 complete gene list DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, COL4A1, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, ALDH18A1, FBN1, ATP6V0A2, PYCR1, ELN, COL3A1, COL1A2, COL1A1, FBLN5, B4GALT7, ATP7A Specificity 5 % Genes 19 %
Connective tissue disorders - Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, Aortic Aneurysm. By CeGaT GmbH in Germany. DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...) View the complete list with 24 more genes Panel GTR000522401 complete gene list DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, COL4A1, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, ALDH18A1, FBN1, ATP6V0A2, PYCR1, ELN, COL3A1, COL1A2, COL1A1, FBLN5, B4GALT7, ATP7A Specificity 5 % Genes 19 %
Potentially lethal skeletal disorders Panel. By CeGaT GmbH in Germany. WDR34, INPPL1, GDF5, TRIP11, SLC35D1, LIFR, FLNB, DLL3, FAM111A, RNU4ATAC, BMPER, ARSE, NEK1, WNT7A, DYNC2H1, TCTN3, IFT80, GNPAT, GLI3, SOX9 , (...) View the complete list with 24 more genes Panel GTR000527958 complete gene list WDR34, INPPL1, GDF5, TRIP11, SLC35D1, LIFR, FLNB, DLL3, FAM111A, RNU4ATAC, BMPER, ARSE, NEK1, WNT7A, DYNC2H1, TCTN3, IFT80, GNPAT, GLI3, SOX9, NSDHL, EBP, PTH1R, CANT1, COL11A2, COL11A1, LBR, OFD1, FLNA, TRPV4, SLC26A2, PEX7, FGFR2, DHCR7, FGFR3, PPIB, FAM20C, AGPS, CRTAP, P3H1, COL1A2, COL1A1, COL2A1, ALPL Specificity 12 % Genes 46 %
Skeletal dysplasia with increased bone density Panel. By CeGaT GmbH in Germany. SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, DHCR24, GJA1, PTH1R, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1 , (...) View the complete list with 8 more genes Panel GTR000527963 complete gene list SLCO2A1, SNX10, PLEKHM1, DLX3, MTAP, HPGD, PTDSS1, LRP4, TBXAS1, DHCR24, GJA1, PTH1R, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, ANKH Specificity 4 % Genes 10 %
Osteogenesis imperfecta. By Laboratory of Human Genetics GENOMED Health Care Center in Poland. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers-Danlos Syndrome. By Laboratory of Human Genetics GENOMED Health Care Center in Poland. PLOD1, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 34 % Genes 19 %
COL1A1/2-Related Osteogenesis Imperfecta. By Innovagenomics Innovagenomics S.L in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Caffey Disease, COL1A1. By GGA - Galil Genetic Analysis in Israel. COL1A1 Specificity 100 % Genes 10 %
COL1A1/2-Related Osteogenesis Imperfecta. By MVZ Dortmund Dr. Eberhard & Partner in Germany. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Ehlers-Danlos Syndrome, Arthrochalasia Type (EDS VIIA/VIIB). By MVZ Dortmund Dr. Eberhard & Partner in Germany. COL1A2, COL1A1 Specificity 100 % Genes 19 %
OI panel 1. By Connective Tissue Laboratory Ghent University Hospital in Belgium. COL1A2, COL1A1, IFITM5 Specificity 67 % Genes 19 %
COL1A1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. COL1A1 Specificity 100 % Genes 10 %
Caffey disease, COL1A1, R836C sequencing. By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta (OI), COL1A1/COL1A2 sequencing. By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Inherited Cardiovascular Diseases and Sudden Death Panel. By Health in Code in Spain. FHOD3, FOXD4, SMAD1, TRIM63, KLF10, LRP6, CALR3, MIB1, TBX20, CAVIN4, APOC3, ADAMTSL4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA , (...) View the complete list with 193 more genes Panel GTR000521465 complete gene list FHOD3, FOXD4, SMAD1, TRIM63, KLF10, LRP6, CALR3, MIB1, TBX20, CAVIN4, APOC3, ADAMTSL4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA, GATA6, APOA5, APOB, PCSK9, CETP, CRELD1, GATA4, TMPO, TXNRD2, FHL2, CTF1, GJA1, TBX5, PRKG1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, PRDM16, LAMA4, TGFB3, MYLK2, ACTC1, NEBL, PDLIM3, BMPR2, KCNA5, SMAD9, CAV1, KCNK3, GDF2, BMPR1B, ACVRL1, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, SPRED1, LAMP2, CACNA1C, KCNQ1, KCNE1, CACNA1D, TBX1, CACNA2D1, FLNA, SCN5A, HCN4, SCN1B, KCNH2, LAMA2, KCND3, KCNJ2, SGCD, TCAP, EMD, TMEM43, ACTA1, MYBPC3, FHL1, BAG3, BSCL2, LDB3, MYOT, FLNC, MYH7, DES, TTN, CAV3, FKRP, NOTCH3, PSEN2, LMNA, CAPN3, SGCB, SGCA, FKTN, ENG, SMAD4, CBL, MAP2K2, SOS1, SHOC2, PTPN11, PLOD1, NRAS, MAP2K1, LDLR, KRAS, HRAS, GLA, DMD, BRAF, DOLK, COL5A2, COL5A1, ALMS1, PMM2, SLC22A5, COX6B1, CBS, MLYCD, GUSB, SURF1, COX15, PHKA1, TAZ, PDHA1, COQ2, GFM1, DNAJC19, TSFM, MRPS22, FAH, TMEM70, AGK, LIAS, MRPL3, MTO1, FBN1, RAF1, CRYAB, SLC25A4, DLD, DSP, JAG1, PITX2, GLB1, GNPTAB, EYA4, ELN, PSEN1, COL3A1, COL1A2, COL1A1, GAA, ATPAF2, ACADVL, AGL, ACADM, ACAD9, AARS2, TTR, HFE Specificity 1 % Genes 19 %
Aortic Valvular Diseases Panel. By Health in Code in Spain. ADAMTSL4, PRKG1, NKX2-5, TGFB3, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, SMAD4, PTPN11, PLOD1 , (...) View the complete list with 10 more genes Panel GTR000521466 complete gene list ADAMTSL4, PRKG1, NKX2-5, TGFB3, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, SMAD4, PTPN11, PLOD1, HRAS, COL5A2, COL5A1, CBS, FBN1, ELN, COL3A1, COL1A2, COL1A1, GAA Specificity 7 % Genes 19 %
Cardiovascular Diseases_General Panel. By Health in Code in Spain. CH25H, BMP10, TRIB1, TOPBP1, ISL1, GREM2, HAND2, SLC25A40, NNT, PPARA, MYOM1, LPA, SLC22A8, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, SMAD1 , (...) View the complete list with 360 more genes Panel GTR000530651 complete gene list CH25H, BMP10, TRIB1, TOPBP1, ISL1, GREM2, HAND2, SLC25A40, NNT, PPARA, MYOM1, LPA, SLC22A8, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, SMAD1, IRX4, MCTP2, CYP3A5, NKX2-6, MRPL44, KCND2, MED13L, COA6, TRIM63, KLF10, PKP4, LRP6, INSIG2, CYP3A4, TNNI3K, TAB2, SMAD6, TFAP2B, SAR1B, MYLIP, CALM3, ASPH, CALR3, MIB1, TBX20, EIF2AK4, SLCO1B1, CAVIN4, CHRM2, PLTP, LIPC, APOC3, GATA5, ADAMTSL4, KCNE5, CTNNA3, SCN10A, COA5, FGF12, OBSL1, ANK3, ZFPM2, AGPAT2, PLIN1, CIDEC, TBC1D4, NOTCH2, GJA5, NPPA, COL7A1, TDGF1, XK, CFC1, INSR, PDGFRA, EIF2AK3, GATA6, PTF1A, NEUROG3, GLIS3, BLK, KLF11, PAX4, RFX6, AKT2, SLC2A2, ABCA1, LCAT, ABCG1, ANGPTL3, GPIHBP1, APOC2, LMF1, LPL, APOA5, APOB, LDLRAP1, PCSK9, APOA1, SCARB1, CETP, ACVR2B, CRELD1, LEFTY2, CITED2, NPC1L1, IER3IP1, EVC, GATA4, GDF1, ZIC3, TMPO, TXNRD2, OBSCN, CYP2D6, ABCG8, ABCG5, B3GAT3, FHL2, GJA1, EP300, TBX5, SALL4, NOS1AP, MFAP5, PRKG1, ZMPSTE24, SPEG, TOR1AIP1, AMPD1, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, PRDM16, LAMA4, TGFB3, MYLK2, ACTC1, NEBL, ILK, PDLIM3, BMPR2, KCNA5, EFEMP2, SMAD9, CAV1, KCNK3, GDF2, BMPR1B, ACVRL1, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, ACVR1, CHST14, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FOXH1, NODAL, ABCB1, A2ML1, RRAS, RASA2, SPRED1, ZDHHC9, UPF3B, LAMP2, FOXP3, RASA1, LZTR1, CTNNB1, CACNA1C, EHMT1, FOXP1, VCL, MED12, KCNQ1, KCNE1, CACNA1D, TBX1, KANSL1, CACNA2D1, KMT2D, FLNA, SCN5A, HCN4, SCN1B, KCNH2, LAMA2, KCND3, KCNJ2, SGCD, TCAP, EMD, SYNE2, TMEM43, SYNE1, ACTA1, MYBPC3, RYR1, FHL1, BAG3, BSCL2, LDB3, MYOT, ANO5, FLNC, MYH7, DES, TTN, PDX1, INS, KCNJ11, CEL, NF1, CAV3, FKRP, NOTCH3, APOE, PSEN2, LMNA, CAPN3, SGCB, SGCA, MTTP, FKTN, ADAMTS2, ENG, SMAD4, BMPR1A, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, PLOD1, NRAS, MAP2K1, LIPA, LEP, LDLR, KRAS, HRAS, GLA, FOXF1, DMD, CREBBP, CHD7, BRAF, DOLK, SDHA, COL5A2, COL5A1, ZFHX3, ALMS1, PMM2, SLC22A5, COX6B1, FXN, PYGM, CBS, MLYCD, GUSB, SURF1, COX15, PHKA1, TAZ, PDHA1, SCO2, COQ2, MEF2A, GFM1, DNAJC19, TSFM, PNPLA2, SLC25A3, MRPS22, SLC39A13, CAVIN1, IDH2, FAH, TMEM70, DNM1L, AGK, GPD1, LIAS, MRPL3, MTO1, FBN1, OPA3, RAF1, CRYAB, FOXRED1, GCK, SLC25A4, DLD, DSP, PCDH15, NPHP4, JAG1, PITX2, FOXC1, GLB1, GNPTAB, WFS1, CPT2, EYA4, ELN, HNF1B, PSEN1, ELAC2, COL3A1, COL1A2, COL1A1, PPARG, NEUROD1, HNF1A, GAA, B4GALT7, ATPAF2, ATP7A, ATP5F1E, ACADVL, AGL, ACAD9, AARS2, TTR, HNF4A, HFE Specificity 1 % Genes 19 %
Aortic diseases Panel. By Health in Code in Spain. GATA5, ADAMTSL4, B3GAT3, PRKG1, NKX2-5, TGFB3, EFEMP2, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, ZDHHC9 , (...) View the complete list with 15 more genes Panel GTR000530671 complete gene list GATA5, ADAMTSL4, B3GAT3, PRKG1, NKX2-5, TGFB3, EFEMP2, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, ZDHHC9, MED12, FLNA, SMAD4, PTPN11, PLOD1, HRAS, COL5A2, COL5A1, CBS, FBN1, ELN, COL3A1, COL1A2, COL1A1, GAA Specificity 6 % Genes 19 %
Osteogenesis Imperfecta. By Molecular Vision Laboratory in United States. P3H1, COL1A2, COL1A1 Specificity 100 % Genes 28 %
COL1A1. By Molecular Vision Laboratory in United States. COL1A1 Specificity 100 % Genes 10 %
aCGH Deletion/Duplication Analysis. By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States. SERPIND1, HRG, PLA2G4A, C4BPB, C4BPA, LMAN1, SERPINC1, F13A1, F10, GP9, ACTN1, CFHR4, F7, VKORC1, PROC, RBM8A, G6PC3, STXBP2, ELANE, GP1BB , (...) View the complete list with 45 more genes Panel GTR000523364 complete gene list SERPIND1, HRG, PLA2G4A, C4BPB, C4BPA, LMAN1, SERPINC1, F13A1, F10, GP9, ACTN1, CFHR4, F7, VKORC1, PROC, RBM8A, G6PC3, STXBP2, ELANE, GP1BB, MASTL, HOXA11, PLAU, FGG, TBXA2R, GGCX, FGB, FGA, GP6, GP1BA, ADAMTS13, DGKE, CFHR3, CFHR1, F8, F9, THBD, C3, CD46, CFHR5, CFH, CFI, CFB, VWF, F11, ACVRL1, BLOC1S6, GATA1, MYH9, LMNA, WAS, MPL, ENG, HAX1, CYCS, HPS3, HPS4, HPS5, HPS6, BLOC1S3, HPS1, COL1A1, RUNX1, F5, F2 Specificity 2 % Genes 10 %
Caffey disease. By Praxis fuer Humangenetik Wien in Austria. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome I. By Praxis fuer Humangenetik Wien in Austria. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome VIIA. By Praxis fuer Humangenetik Wien in Austria. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta I. By Praxis fuer Humangenetik Wien in Austria. COL1A1 Specificity 100 % Genes 10 %
Caffey disease. By MedGene in Slovakia. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome I. By MedGene in Slovakia. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome VIIA. By MedGene in Slovakia. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta I. By MedGene in Slovakia. COL1A1 Specificity 100 % Genes 10 %
Invitae Osteogenesis Imperfecta Panel. By Invitae in United States. CRTAP, P3H1, COL1A2, COL1A1 Specificity 100 % Genes 37 %
Invitae Ehlers-Danlos Syndrome Panel. By Invitae in United States. CHST14, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CRTAP, P3H1, SLC39A13, COL3A1, COL1A2, COL1A1, ATP7A Specificity 29 % Genes 37 %
Osteogenesis imperfecta: COL1A1 gene sequence analysis. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta: COL1A1 and COL1A2 genes sequence analysis.. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
EHLERS-DANLOS, SYNDROME. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. CHST14, TNXB, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 19 % Genes 19 %
Skeletal dysplasias. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. MMP9, MMP13, DDR2, MATN3, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, WISP3, ARSE, EVC2, EVC, SOX9, COMP, NSDHL, EBP, PTH1R, COL11A2, COL11A1 , (...) View the complete list with 16 more genes Panel GTR000531666 complete gene list MMP9, MMP13, DDR2, MATN3, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, WISP3, ARSE, EVC2, EVC, SOX9, COMP, NSDHL, EBP, PTH1R, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 6 % Genes 19 %
NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded). By Genome Diagnostics VU University Medical Center in Netherlands. FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL1A2, COL1A1, B4GALT7 Specificity 10 % Genes 19 %
NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + FN1. By Genome Diagnostics VU University Medical Center in Netherlands. FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, FBN1, COL1A2, COL1A1 , (...) View the complete list with 1 more genes Panel GTR000529240 complete gene list FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, FBN1, COL1A2, COL1A1, B4GALT7 Specificity 10 % Genes 19 %
NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded). By Genome Diagnostics VU University Medical Center in Netherlands. FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL1A2, COL1A1, B4GALT7 Specificity 10 % Genes 19 %
NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + COL3A1. By Genome Diagnostics VU University Medical Center in Netherlands. FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL3A1, COL1A2, COL1A1 , (...) View the complete list with 1 more genes Panel GTR000529253 complete gene list FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 10 % Genes 19 %
COL1A1 - Gene Sequencing & Del/Dup analysis. By Genome Diagnostics VU University Medical Center in Netherlands. COL1A1 Specificity 100 % Genes 10 %
NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + FLNA. By Genome Diagnostics VU University Medical Center in Netherlands. FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL1A2, COL1A1 , (...) View the complete list with 1 more genes Panel GTR000529270 complete gene list FLNB, DSE, CHST3, B3GALT6, B3GAT3, COL12A1, ZNF469, CHST14, TNXB, PRDM5, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, PLOD3, COL1A2, COL1A1, B4GALT7 Specificity 10 % Genes 19 %
Connective Tissue Disorders: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS , (...) View the complete list with 9 more genes Panel GTR000512594 complete gene list ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ATP6V0A2, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5 Specificity 7 % Genes 19 %
Disproportionate Short Stature: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. SULF1, KIF22, ACAN, PAPSS2, TBX6, IHH, NPR2, MMP9, MMP13, DDR2, MATN3, GDF5, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, ACP5, DLL3, NKX3-2 , (...) View the complete list with 65 more genes Panel GTR000512595 complete gene list SULF1, KIF22, ACAN, PAPSS2, TBX6, IHH, NPR2, MMP9, MMP13, DDR2, MATN3, GDF5, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, ACP5, DLL3, NKX3-2, CHST3, GPC6, LFNG, HES7, MESP2, TBCE, OBSL1, CUL7, ARSE, NEK1, ICK, ROR2, DYNC2H1, WNT5A, TCTN3, SMARCAL1, EXT1, EXT2, DHCR24, EIF2AK3, IFT122, B3GALT6, EVC2, EVC, IFT80, BMPR1B, SH3PXD2B, IFT140, GLI3, CHST14, DYM, PCNT, SOX9, COMP, EBP, PTH1R, CANT1, WDR35, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, FLNA, HSPG2, ANO5, SHOX, FGFR1, TRPV4, SLC26A2, PRKAR1A, CDKN1C, FGFR2, RUNX2, PTPN11, COL10A1, FGFR3, FAM20C, CTSK, AGPS, SLC39A13, FBN1, COL1A1, COL2A1, ANKH Specificity 2 % Genes 10 %
Skeletal Dysplasia With Increased Bone Density: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. RASGRP2, DLX3, HPGD, GALNT3, LRP4, TBXAS1, FERMT3, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, CTSK, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5 , (...) View the complete list with 2 more genes Panel GTR000512614 complete gene list RASGRP2, DLX3, HPGD, GALNT3, LRP4, TBXAS1, FERMT3, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, CTSK, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, TYROBP, ANKH Specificity 5 % Genes 10 %
Connective Tissue Disorders: Deletion/Duplication Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS , (...) View the complete list with 9 more genes Panel GTR000558816 complete gene list ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ATP6V0A2, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5 Specificity 7 % Genes 19 %
Disproportionate Short Stature: Deletion/Duplication Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. SULF1, KIF22, PAPSS2, IHH, NPR2, MMP9, MMP13, DDR2, MATN3, GDF5, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, ACP5, NKX3-2, CHST3, GPC6, TBCE , (...) View the complete list with 56 more genes Panel GTR000558820 complete gene list SULF1, KIF22, PAPSS2, IHH, NPR2, MMP9, MMP13, DDR2, MATN3, GDF5, TRPS1, TRIP11, SLC35D1, LIFR, FLNB, ACP5, NKX3-2, CHST3, GPC6, TBCE, OBSL1, CUL7, NEK1, ICK, ROR2, DYNC2H1, WNT5A, TCTN3, SMARCAL1, EXT1, EXT2, DHCR24, EIF2AK3, IFT122, B3GALT6, EVC2, EVC, IFT80, BMPR1B, SH3PXD2B, IFT140, GLI3, CHST14, DYM, PCNT, SOX9, COMP, PTH1R, CANT1, WDR35, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, FLNA, HSPG2, ANO5, SHOX, FGFR1, TRPV4, SLC26A2, PRKAR1A, CDKN1C, FGFR2, RUNX2, PTPN11, COL10A1, FGFR3, FAM20C, CTSK, SLC39A13, FBN1, COL1A1, COL2A1, ANKH Specificity 2 % Genes 10 %
Connective Tissue NGS Panel. By Fulgent Genetics Fulgent Genetics in United States. ACVR1, ZNF469, ABCC6, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, COL4A1, PKD2, ADAMTS2, PLOD1, COL5A2 , (...) View the complete list with 11 more genes Panel GTR000509372 complete gene list ACVR1, ZNF469, ABCC6, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, COL4A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ATP6V0A2, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5 Specificity 7 % Genes 19 %
Osteogenesis Imperfecta NGS Panel. By Fulgent Genetics Fulgent Genetics in United States. COL1A2, COL1A1 Specificity 100 % Genes 19 %
COL1A1. By Fulgent Genetics Fulgent Genetics in United States. COL1A1 Specificity 100 % Genes 10 %
OSTEOGENON. By PentaCoreLab in Hungary. CRTAP, P3H1, COL1A2, COL1A1 Specificity 100 % Genes 37 %
Ehlers-Danlos. By PentaCoreLab in Hungary. TNXB, ADAMTS2, PLOD1, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 25 % Genes 19 %
Hemato-oncology chromosomal microarray. By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States. NUTM2B, NUTM2A, SSX2, MALAT1, ETV4, TFEB, SSX4, NR4A3, MSI2, CREB3L2, TFE3, FOXO1, ETV1, ACSL3, RABEP1, SSX1, SS18, POU5F1, HEY1, JUN , (...) View the complete list with 72 more genes Panel GTR000527837 complete gene list NUTM2B, NUTM2A, SSX2, MALAT1, ETV4, TFEB, SSX4, NR4A3, MSI2, CREB3L2, TFE3, FOXO1, ETV1, ACSL3, RABEP1, SSX1, SS18, POU5F1, HEY1, JUN, ASPSCR1, LMO1, MAP2K4, PATZ1, PBRM1, DDIT3, FEV, ERG, NCOA2, NCOA1, HIP1, CREB1, FOXA1, PAX7, TAF15, EWSR1, ABI1, SS18L1, NTRK3, CCNE1, PPP2R1A, CIC, SMO, YWHAE, PTCH2, ERBB2, CHN1, CDK12, CCND1, KDR, DICER1, TCF12, FLI1, PIK3R1, STAT5B, EXT1, EXT2, AKT1, ETV6, STAG2, HOXA11, AKT2, MYCN, PIK3CA, BAP1, CREB3L1, DUX4, EP300, SMARCB1, TERT, CTNNB1, GATA3, PAX3, KDM5C, SETD2, FUS, CDH1, SUFU, PHOX2B, PTCH1, ALK, HRAS, BRAF, BLM, RB1, COL1A1, TP53, MLH1, MSH2, APC, BRCA2, BRCA1 Specificity 3 % Genes 19 %
Osteopetrosis and Dense Bone Dysplasia Panel. By Blueprint Genetics in Finland. SLCO2A1, SNX10, DLX3, PTDSS1, LRP4, SLC29A3, GJA1, PTH1R, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1 , (...) View the complete list with 5 more genes Panel GTR000552716 complete gene list SLCO2A1, SNX10, DLX3, PTDSS1, LRP4, SLC29A3, GJA1, PTH1R, TNFRSF11B, TCIRG1, TNFSF11, OSTM1, CA2, FAM20C, CTSK, AMER1, CLCN7, TNFRSF11A, LEMD3, TGFB1, SOST, COL1A1, LRP5, TYROBP, ANKH Specificity 4 % Genes 10 %
Marfan Syndrome Panel. By Blueprint Genetics in Finland. ADAMTS17, VCAN, SMAD6, ADAMTS10, ADAMTSL4, ABL1, BGN, MAT2A, TGFB3, EFEMP2, SLC2A10, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, UPF3B, MED12, COL11A2 , (...) View the complete list with 10 more genes Panel GTR000552717 complete gene list ADAMTS17, VCAN, SMAD6, ADAMTS10, ADAMTSL4, ABL1, BGN, MAT2A, TGFB3, EFEMP2, SLC2A10, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, UPF3B, MED12, COL11A2, COL11A1, PLOD1, COL5A2, COL5A1, CBS, FBN1, COL3A1, COL1A2, COL1A1, COL2A1 Specificity 7 % Genes 19 %
Aorta Panel. By Blueprint Genetics in Finland. ADAMTS17, SMAD6, ADAMTS10, GATA5, ADAMTSL4, ENPP1, ABL1, BGN, SMAD2, MAT2A, MFAP5, TGFB3, EFEMP2, ZNF469, ABCC6, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...) View the complete list with 21 more genes Panel GTR000552671 complete gene list ADAMTS17, SMAD6, ADAMTS10, GATA5, ADAMTSL4, ENPP1, ABL1, BGN, SMAD2, MAT2A, MFAP5, TGFB3, EFEMP2, ZNF469, ABCC6, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, ALDH18A1, FBN1, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5 Specificity 5 % Genes 19 %
Ehlers-Danlos Syndrome Panel. By Blueprint Genetics in Finland. DSE, BGN, EFEMP2, ZNF469, ABCC6, CHST14, FKBP14, FBN2, TGFBR2, TGFBR1, SMAD3, TGFB2, COL11A1, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13 , (...) View the complete list with 12 more genes Panel GTR000552678 complete gene list DSE, BGN, EFEMP2, ZNF469, ABCC6, CHST14, FKBP14, FBN2, TGFBR2, TGFBR1, SMAD3, TGFB2, COL11A1, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, ALDH18A1, FBN1, ATP6V0A2, PYCR1, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5, B4GALT7, ATP7A Specificity 7 % Genes 19 %
Osteogenesis Imperfecta type II. By Bioarray in Spain. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome, arthrochalasic type. By Bioarray in Spain. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta. By Bioarray in Spain. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta type I. By Bioarray in Spain. COL1A1 Specificity 100 % Genes 10 %
Exome. By DNA CONSULT GENETICA E BIOTECNOLOGIA LTDA. in Brazil. IPW, SMNDC1, GEMIN2, HERC2, ATXN8, CYP2C9, IL1RN, CCDC88C, VKORC1, CYP2D6, CYP2C19, F8, F9, MAGEL2, SOX9, RPL10, PTCHD1, SEMA3E, SHANK2, KCND3 , (...) View the complete list with 46 more genes Panel GTR000530118 complete gene list IPW, SMNDC1, GEMIN2, HERC2, ATXN8, CYP2C9, IL1RN, CCDC88C, VKORC1, CYP2D6, CYP2C19, F8, F9, MAGEL2, SOX9, RPL10, PTCHD1, SEMA3E, SHANK2, KCND3, ATXN8OS, TBP, ATXN2, SERPINA1, CDH1, TSC1, ATXN1, PTPN11, NRAS, DMPK, MAP2K1, KRAS, IDS, DMD, CHD7, CDKL5, BRAF, CFTR, FGFR3, COL5A2, COL5A1, MEN1, FXN, ABCD1, FBN1, MECP2, AFG3L2, RET, TGFB1, PRKCG, COL3A1, COL1A2, COL1A1, COL2A1, ALPL, TP53, PTEN, MUTYH, APC, UBE3A, TTR, HFE, HTT, FMR1, BRCA2, BRCA1 Specificity 4 % Genes 19 %
Ehlers-Danlos Syndrome, Type I Panel by NGS. By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada. COL5A2, COL5A1, COL1A1 Specificity 34 % Genes 10 %
COL1A1 Gene, entire coding region or targeted variant. By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada. COL1A1 Specificity 100 % Genes 10 %
Caris MI TumorSeek 592-Gene NGS Panel. By Caris Life Sciences in United States. ETV1, BCL3, SET, ELL, BTG1, ADGRA2, ACSL3, AFF1, ACSL6, ACKR3, RABEP1, PSIP1, RANBP17, RAD51B, RPL22, SDC4, SH3GL1, REL, SLC45A3, SYK , (...) View the complete list with 571 more genes Panel GTR000560898 complete gene list ETV1, BCL3, SET, ELL, BTG1, ADGRA2, ACSL3, AFF1, ACSL6, ACKR3, RABEP1, PSIP1, RANBP17, RAD51B, RPL22, SDC4, SH3GL1, REL, SLC45A3, SYK, TCL1A, SPECC1, SPEN, SNX29, SOCS1, SPOP, SSX1, SS18, STAT4, SRGAP3, TCEA1, SRSF3, ZNF331, THRAP3, NSD3, TFRC, SEPT5, TFPT, WWTR1, XPO1, ZNF217, ZNF521, ZMYM2, TRIM27, TLX3, TNFRSF17, TTL, TPR, TRAF7, TRRAP, TNFRSF14, TRIM26, VEGFB, USP6, TMPRSS2, VTI1A, PLAG1, PRCC, POU2AF1, PIM1, POU5F1, PRDM1, HERPUD1, HIST1H3B, HEY1, JAK1, JUN, HOOK3, HOXA9, KLHL6, IL6ST, JAZF1, IKBKE, HSP90AB1, HSP90AA1, KLK2, ASPSCR1, LRP1B, LCP1, LGR5, LPP, ARNT, BCL2L11, ARHGEF12, BCL2L2, AURKB, LMO1, KTN1, ATF1, LRIG3, LASP1, ARFRP1, ARHGAP26, LHFPL6, AFDN, MLLT11, MDM4, MLLT10, MAP2K4, BCL9, BRD3, MRTFA, MCL1, EMSY, MAML2, WDCP, BCL7A, MSN, NUTM1, CARS, CHCHD7, CHEK1, CHIC2, CNOT3, NUP98, OMD, CRTC1, CRTC3, COPB1, CNTRL, PDE4DIP, DDX6, PATZ1, PCSK7, DDX5, PDCD1, PBRM1, DDIT3, DAXX, PAFAH1B2, DDX10, PDCD1LG2, EPHB1, ELK4, PER1, EIF4A2, EPHA3, EBF1, DOT1L, EPHA5, EPS15, ECT2L, ELF4, FEV, FGF6, FCRL4, ERC1, FBXO11, ERG, FHIT, TENT5C, FOXO4, FOXO3, MTCP1, HOXD11, HIST1H4I, TLX1, CCDC6, CBFA2T3, FSTL3, RMI2, TPM4, C15orf65, OLIG2, COX6C, HLF, MLLT6, SEPT6, TAL2, HOXC11, LMO2, FNBP1, RAP1GDS1, FGFR1OP, MDS2, LYL1, SFPQ, GMPS, WIF1, TRIM33, H3F3B, GID4, ZNF703, MEF2B, AURKA, TOP1, P2RY8, FGF4, SUZ12, FGF19, H3F3A, KLF4, BCL11B, NUTM2B, ETV4, TFEB, NR4A3, MSI2, CREB3L2, TFE3, FOXO1, CD74, RAC1, RICTOR, RALGDS, KDM5A, ATP1A1, ERBB4, PPP2R1A, CLTC, SLC34A2, CIC, TET1, BCL11A, AXL, NONO, CLTCL1, PRRX1, NUP93, RNF43, HOXC13, CDKN2C, MECOM, RPN1, BIRC3, MYC, BCL6, SMO, YWHAE, CDKN2B, MLLT1, CLP1, MLLT3, MN1, NUP214, AFF3, TAL1, ZBTB16, FIP1L1, PBX1, TCF3, RARA, ERCC1, CBFB, ERBB2, HNRNPA2B1, PICALM, NUMA1, DEK, PML, CHN1, MAFB, RNF213, GPHN, DDR2, MDM2, IGF1R, ETV5, MALT1, IL21R, ABL2, DDB2, CDK12, BCL2, CCND1, XPC, KAT6A, CD79B, CD79A, TRIP11, LIFR, KIAA1549, KDSR, TNFAIP3, ZNF384, KDR, FLT1, CYLD, HOXD13, WISP3, NSD2, BUB1B, RAD51, XPA, ERCC5, CAMTA1, ATP2B3, PDGFB, PDGFRB, DICER1, PAX8, WRN, TCF12, NIN, CTCF, EZR, KNL1, CDK6, MUC1, FLI1, RUNX1T1, SRC, MAP3K1, HOXA13, CCND2, MNX1, NTRK2, AFF4, CARD11, POT1, NOTCH2, PRKDC, PIK3R1, CTLA4, NFKB2, CIITA, NFKBIA, BCR, PTPRC, STAT5B, ITK, FAS, EXT1, EXT2, AKT1, AKT3, PIK3R2, GNA11, IL7R, CBLC, BCORL1, CBLB, CSF3R, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, EGFR, NPM1, FLT3, HOXA11, GNAQ, AKT2, CSF1R, GAS7, FUBP1, NCOA2, CD274, NCOA1, CDK8, CCND3, NFIB, MYB, CDH11, CCNB1IP1, CDX2, NACA, NCKIPSD, GOPC, GSK3B, TCF7L2, GOLGA5, HIP1, HMGA2, IRF4, HMGA1, PCM1, IRS2, CREB1, RBM15, FOXA1, PIK3CG, CRKL, PAX7, RHOH, TAF15, EWSR1, UBR5, AXIN1, ABI1, CRLF2, MLF1, INHBA, LCK, IL2, BCL10, ESR1, SS18L1, KMT2C, FGFR4, NTRK3, MYCL, ROS1, RPTOR, KIF5B, GNA13, EML4, BRD4, ARAF, NFE2L2, KEAP1, CCNE1, MYCN, PIK3CA, ERCC4, VEGFA, CDKN1B, BAP1, CYP2D6, FANCD2, FANCL, FANCE, FANCF, FANCG, FANCA, SMAD2, CREB3L1, GNAS, CALR, SH2B3, JAK3, ASXL1, KIT, EP300, FGF10, FLT4, NT5C2, ARID1A, SMARCB1, SMARCA4, KMT2A, SMARCE1, ARID2, ERBB3, PRDM16, NKX2-1, TERT, MAF, CTNNA1, TFG, KDM6A, AKAP9, KCNJ5, MITF, EZH2, DNMT3A, MYH11, TGFBR2, NOTCH1, ATR, MTOR, RPL10, CANT1, RPL5, GATA1, KAT6B, CTNNB1, FOXP1, MED12, MYH9, GATA3, FGF3, SOX10, PAX3, ERCC3, ERCC2, HGF, CACNA1D, SETBP1, KDM5C, PAK3, PHF6, ATRX, TBL1XR1, SETD2, KMT2D, STIL, GRIN2A, FGF14, TPM3, FUS, PDK1, FGF23, FGFR1, NF1, CNBP, NTRK1, DNM2, NDRG1, BTK, WAS, MPL, PMS1, BARD1, CDC73, PRKAR1A, PRF1, CEBPA, SBDS, PAX5, GATA2, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, GPC3, MET, FLCN, SDHD, CDKN2A, CDK4, STK11, CDH1, SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, MRE11, ATM, ALK, NSD1, TSC1, CBL, RAD21, TSC2, MAP2K2, FGFR2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, CREBBP, BRAF, BLM, FANCC, AR, FGFR3, TSHR, MEN1, STAT3, SEPT9, NCOA4, SOX2, BCOR, AMER1, ATIC, ALDH2, SDHB, IDH2, FH, RAF1, POLE, SDHC, CASP8, ELN, RET, SDHAF2, RB1, WT1, COL1A1, PPARG, HNF1A, FOXL2, TP53, RUNX1, RECQL4, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC, VHL, BRCA2, BRCA1 Specificity 1 % Genes 19 %
OSTEOGENESIS IMPERFECTA (AUTOSOMAL DOMINANT). By Laboratorio de Genetica Clinica SL in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
EHLERS-DANLOS SYNDROME, ARTROCALASIA, TYPE 7A & 7B. By Laboratorio de Genetica Clinica SL in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
EHLERS-DANLOS SYNDROME: NGS PANEL-1. By Laboratorio de Genetica Clinica SL in Spain. TNXB, PLOD1, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 29 % Genes 19 %
EHLERS-DANLOS SYNDROME: NGS PANEL-2. By Laboratorio de Genetica Clinica SL in Spain. DSE, B3GALT6, CHST14, TNXB, FKBP14, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 14 % Genes 19 %
Ehlers-Danlos syndrome and related disorders panel. By LifeLabs Genetics in Canada. FKBP14, PLOD1, COL5A2, COL5A1, COL3A1, COL1A2, COL1A1 Specificity 29 % Genes 19 %
Osteogenesis Imperfecta , Deletions-Duplications (MLPA) COL1A1 Gene. By Reference Laboratory Genetics in Spain. COL1A1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Panel massive Sequencing (NGS) (COL1A1,COL1A2) Genes. By Reference Laboratory Genetics in Spain. COL1A2, COL1A1 Specificity 100 % Genes 19 %
Osteogenesis Imperfecta , Massive Sequencing COL1A1 Gene. By Reference Laboratory Genetics in Spain. COL1A1 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndrome , Panel Massive Sequencing (NGS) 13 Genes. By Reference Laboratory Genetics in Spain. B3GALT6, CHST14, TNXB, FKBP14, ADAMTS2, PLOD1, COL5A2, COL5A1, SLC39A13, COL3A1, COL1A2, COL1A1, B4GALT7 Specificity 16 % Genes 19 %
Conective Tissue Related Disorders , Panel Massive Sequencing (NGS) 39 Genes. By Reference Laboratory Genetics in Spain. ADAMTS10, TGFB3, EFEMP2, ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2 , (...) View the complete list with 19 more genes Panel GTR000559846 complete gene list ADAMTS10, TGFB3, EFEMP2, ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A2, COL11A1, COL9A2, COL9A1, ADAMTS2, SMAD4, PLOD1, COL5A2, COL5A1, CBS, SLC39A13, FBN1, ATP6V0A2, ELN, COL3A1, COL1A2, COL1A1, COL2A1, FBLN5 Specificity 6 % Genes 19 %
Skeletal Dysplasias , Panel Massive Sequencing (NGS) 36 Genes. By Reference Laboratory Genetics in Spain. MMP9, MMP13, DDR2, MATN3, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, WISP3, ARSE, EVC2, EVC, SOX9, COMP, NSDHL, EBP, PTH1R, COL11A2, COL11A1 , (...) View the complete list with 16 more genes Panel GTR000559863 complete gene list MMP9, MMP13, DDR2, MATN3, TRIP11, SLC35D1, LIFR, FLNB, NKX3-2, WISP3, ARSE, EVC2, EVC, SOX9, COMP, NSDHL, EBP, PTH1R, COL11A2, COL11A1, COL9A2, COL9A3, COL9A1, LBR, HSPG2, TRPV4, SLC26A2, PEX7, SBDS, RMRP, COL10A1, FGFR3, COL1A2, COL1A1, COL2A1, ALPL Specificity 6 % Genes 19 %
Osteoporosis Susceptibility to , Panel Massive Sequencing (NGS) 5 Genes. By Reference Laboratory Genetics in Spain. CALCR, VDR, COL1A2, COL1A1, LRP5 Specificity 40 % Genes 19 %
COL1A2 Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. COL1A2 Specificity 100 % Genes 10 %
COL1A2 Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. COL1A2 Specificity 100 % Genes 10 %
COL1A2 Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. COL1A2 Specificity 100 % Genes 10 %
COL1A2 (OI) DNA Sequencing Test. By Athena Diagnostics Inc in United States. COL1A2 Specificity 100 % Genes 10 %
COL1A2 Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States. COL1A2 Specificity 100 % Genes 10 %
COL1A2. By Institute for Human Genetics University Clinic Freiburg in Germany. COL1A2 Specificity 100 % Genes 10 %
COL1A2. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A2 Specificity 100 % Genes 10 %
COL1A2. MLPA testing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta (sequence analysis of COL1A2 gene). By CGC Genetics in Portugal. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome type VIIB (sequence analysis of COL1A2 gene). By CGC Genetics in Portugal. COL1A2 Specificity 100 % Genes 10 %
Deletion/duplication analysis of COL1A2 gene. By CGC Genetics in Portugal. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome (deletion/duplication analysis of COL1A2 gene). By CGC Genetics in Portugal. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome (deletion/duplication analysis of COL1A2 gene). By CGC Genetics in Portugal. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via the COL1A2 Gene. By PreventionGenetics PreventionGenetics in United States. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, types I, II, III & IV NGS Test B. By Connective Tissue Gene Tests in United States. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, types I, II, III & IV Comprehensive Test B. By Connective Tissue Gene Tests in United States. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, types I, II, III & IV Deletion / Duplication Test B. By Connective Tissue Gene Tests in United States. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndrome Type VIIB. By Bioscientia GmbH Center for Human Genetics in Germany. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome type VIIC. By Centogene AG - the Rare Disease Company in Germany. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta. By Centogene AG - the Rare Disease Company in Germany. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndrome Type VIIB. By bio.logis Center for Human Genetics Diagnosticum in Germany. COL1A2 Specificity 100 % Genes 10 %
COL1A2 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. COL1A2 Specificity 100 % Genes 10 %
COL1A2 single gene sequencing. By Molecular Vision Laboratory in United States. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome VIIB. By Praxis fuer Humangenetik Wien in Austria. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta III. By Praxis fuer Humangenetik Wien in Austria. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta II. By Praxis fuer Humangenetik Wien in Austria. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta IV. By Praxis fuer Humangenetik Wien in Austria. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome VIIB. By MedGene in Slovakia. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta II. By MedGene in Slovakia. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta III. By MedGene in Slovakia. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta IV. By MedGene in Slovakia. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta: COL1A2 gene sequence analysis. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. COL1A2 Specificity 100 % Genes 10 %
COL1A2 - Gene Sequencing & Del/Dup analysis. By Genome Diagnostics VU University Medical Center in Netherlands. COL1A2 Specificity 100 % Genes 10 %
Intellectual Disability NGS Panel. By Fulgent Genetics Fulgent Genetics in United States. AQP7, TPH2, AFP, XIST, SNIP1, ZBTB24, GLUL, DIP2B, KCNK9, UPB1, CEP57, FTO, ZBTB16, TMCO1, IRX5, AGT, IGF1R, MRAP, HDAC4, IGF1 , (...) View the complete list with 372 more genes Panel GTR000509442 complete gene list AQP7, TPH2, AFP, XIST, SNIP1, ZBTB24, GLUL, DIP2B, KCNK9, UPB1, CEP57, FTO, ZBTB16, TMCO1, IRX5, AGT, IGF1R, MRAP, HDAC4, IGF1, GLRA1, SLC5A2, TRHR, FAM126A, HOXD10, NGF, AVP, AP1S1, BUB1B, WDR81, UROC1, ERCC5, CAMTA1, CEP41, KIF7, RPGRIP1L, SLC6A4, SATB2, CP, SLX4, ABCG5, FANCG, GNAS, NHP2, CTC1, GNPAT, EFNB1, ALX4, THRB, LHX3, PGK1, KIF11, AP4M1, AP4E1, AP4B1, AP4S1, ADAR, ARID1A, SMARCB1, SMARCA4, ERCC6, SDCCAG8, SLC4A4, LYST, GAN, GLI3, GNPTG, ABCC6, FBN2, NAGA, PCNT, ZIC2, TGIF1, NSUN2, TWIST1, IL1RAPL1, ARHGEF6, NSDHL, SOX3, SLC16A2, BRWD3, ZDHHC9, RAB40AL, RBM10, SHROOM4, RPS6KA3, FTSJ1, GDI1, USP9X, UPF3B, UBE2A, TSPAN7, EBP, DLG3, MAGT1, LAMP2, MBTPS2, AFF2, AGTR2, HUWE1, IGBP1, PHF8, CANT1, NLGN3, CTNNB1, ARID1B, AP1S2, EHMT1, FOXP1, KIRREL3, SOX10, ERCC3, ERCC2, SHANK2, SHANK3, LBR, TBX1, GFAP, VPS13B, ZEB2, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, KDM5C, PAK3, GRIA3, SYP, FGD1, IQSEC2, ATRX, SMS, OFD1, CNTNAP2, KCNJ10, SAMHD1, SPTAN1, PIGV, DYRK1A, GRIN1, NRXN1, SCN8A, ST3GAL3, ATP13A2, MFSD8, TUBB2B, SRPX2, PAFAH1B1, TUBA8, PQBP1, PIGO, TBC1D24, MBD5, GRIN2A, GABRG2, CHRNA4, KCNQ2, GRIN2B, PRICKLE1, KCTD7, CPA6, ATP1A2, ASPM, MCPH1, ITGA7, LARGE1, LAMA2, FGF14, GRM1, SIL1, SYT14, POMT1, POMT2, DYNC1H1, BIN1, KIF1A, L1CAM, KIF5A, AVPR2, GHR, POU1F1, KCNJ11, FGFR1, NF1, FKRP, AHI1, MAPT, SCN1A, ZFYVE26, ATL1, SPTLC1, MPZ, TMEM216, DPYD, RAPSN, PLA2G6, POMGNT1, MCOLN1, TH, SACS, SLC7A7, SGCA, PEX7, FKTN, PRKAR1A, BRIP1, CDKN1C, NBN, ATM, NIPBL, TSC1, SMC1A, SYNGAP1, TSC2, HDAC8, FGFR2, WDR62, TINF2, SLC2A1, RAI1, PTPN11, PLP1, PCDH19, NPC2, NPC1, MEF2C, KRAS, IDS, FOXG1, DMD, DHCR7, CHD7, CDKL5, GBA, ARX, AR, FGFR3, TSHR, HPD, PDHX, MTFMT, SLC6A8, KIF21A, PPOX, CLN3, SOX2, BBS9, MGAT2, CYP27A1, ASS1, GLYCTK, GALE, GBE1, CBS, SLC25A15, ALDH4A1, SUCLG1, MAN2B1, MANBA, DBT, CYB5R3, NDUFAF5, NDUFS1, NDUFA1, MOCS2, SGSH, GUSB, CTSA, PAH, ACOX1, SLC35C1, HEXB, GM2A, LMBRD1, MMADHC, ABCD1, SLC9A6, AMER1, ACSL4, AIFM1, D2HGDH, STRA6, MYO7A, MPI, ALG6, ALG12, AP3B1, COG7, GFM1, HAX1, TUSC3, DARS2, TUBA1A, STXBP1, SPR, GAMT, SLC25A12, PHKG2, PYGL, XPNPEP3, PHKA2, TMEM70, ALDH18A1, PDSS1, FBN1, MECP2, SLC25A13, GCK, HSPD1, CEP290, MKKS, NPHP3, TMEM67, NDP, ELOVL4, HSD17B10, SRD5A3, CC2D2A, GNPTAB, PYCR1, ACY1, TBCE, SLC5A5, WRN, ORC1, CC2D1A, CRBN, GRIK2, MAN1B1, PRSS12, TRAPPC9, CDH15, SOBP, MED23, TECR, CACNG2, CRADD, MED17, CCDC88C, PDE4D, ZFP57, HEPACAM, PIGL, TTC37, GSS, STAT5B, LIG4, NHEJ1, G6PC3, STX11, ERCC8, INSR, MYO5A, DHCR24, RFX6, SLC2A2, APOB, MAT1A, SLC20A2, TPK1, SLC46A1, TMEM165, COG5, ALG11, VLDLR, MYCN, RBBP8, CPS1, MTR, TUBB3, PAX6, COL1A2, LRP5, FBLN5, ADSL, BCS1L, AUH, ATP7A, ARG1, GYS2, ACAT1, AGL, MCCC2, MCCC1, PTEN, UBE3A, TTR, MTHFR, FMR1, F5, BRCA2 Specificity 1 % Genes 10 %
COL1A2. By Fulgent Genetics Fulgent Genetics in United States. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta type III. By Bioarray in Spain. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos syndrome, arthrochalasic type. By Bioarray in Spain. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta. By Bioarray in Spain. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Deletions-Duplications (MLPA) COL1A2 Gene. By Reference Laboratory Genetics in Spain. COL1A2 Specificity 100 % Genes 10 %
Ehlers-Danlos Syndrome Type VIIB , Sequencing COL1A2 Gene. By Reference Laboratory Genetics in Spain. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Massive Sequencing COL1A2 Gene. By Reference Laboratory Genetics in Spain. COL1A2 Specificity 100 % Genes 10 %
Osteogenesis imperfecta type XIII (sequence analysis of BMP1 gene). By CGC Genetics in Portugal. BMP1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via BMP1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. BMP1 Specificity 100 % Genes 10 %
BMP1-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. BMP1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, type XIII. By Centogene AG - the Rare Disease Company in Germany. BMP1 Specificity 100 % Genes 10 %
BMP1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. BMP1 Specificity 100 % Genes 10 %
BMP1. By Fulgent Genetics Fulgent Genetics in United States. BMP1 Specificity 100 % Genes 10 %
CREB3L1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. CREB3L1 Specificity 100 % Genes 10 %
CREB3L1. By Fulgent Genetics Fulgent Genetics in United States. CREB3L1 Specificity 100 % Genes 10 %
PPIB Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. PPIB Specificity 100 % Genes 10 %
PPIB Sequence Analysis. By Baylor Miraca Genetics Laboratories in United States. PPIB Specificity 100 % Genes 10 %
PPIB Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. PPIB Specificity 100 % Genes 10 %
PPIB Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. PPIB Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-PPIB. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. PPIB Specificity 100 % Genes 10 %
PPIB. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. PPIB Specificity 100 % Genes 10 %
Osteogenesis imperfecta type IX (sequence analysis of PPIB gene). By CGC Genetics in Portugal. PPIB Specificity 100 % Genes 10 %
PPIB-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. PPIB Specificity 100 % Genes 10 %
Osteogenesis imperfecta type IX. By Centogene AG - the Rare Disease Company in Germany. PPIB Specificity 100 % Genes 10 %
PPIB mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. PPIB Specificity 100 % Genes 10 %
PPIB. By Fulgent Genetics Fulgent Genetics in United States. PPIB Specificity 100 % Genes 10 %
Osteogenesis Imperfecta type IX. By Bioarray in Spain. PPIB Specificity 100 % Genes 10 %
LEPRE1 Sequence Analysis. By Baylor Miraca Genetics Laboratories in United States. P3H1 Specificity 100 % Genes 10 %
LEPRE1 Sequence Analysis (Familial Mutation/Variant Analysis). By Baylor Miraca Genetics Laboratories in United States. P3H1 Specificity 100 % Genes 10 %
LEPRE1 Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. P3H1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-LEPRE1. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. P3H1 Specificity 100 % Genes 10 %
LEPRE 1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. P3H1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta type VIII (sequence analysis of LEPRE1 gene). By CGC Genetics in Portugal. P3H1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via P3H1 / LEPRE1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. P3H1 Specificity 100 % Genes 10 %
LEPRE1-related osteogenesis omperfecta. By Institute of Human Genetics Cologne University in Germany. P3H1 Specificity 100 % Genes 10 %
Cole-Carpenter Syndrome. By Institute of Human Genetics Cologne University in Germany. SEC24D, P3H1 Specificity 50 % Genes 10 %
Osteogenesis imperfecta type VIII. By Centogene AG - the Rare Disease Company in Germany. P3H1 Specificity 100 % Genes 10 %
LEPRE1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. P3H1 Specificity 100 % Genes 10 %
qCarrier Plus. By Quantitative Genomic Medicine Laboratories, SL in Spain. MPP3, FTCD, ADK, CTH, HAL, HGD, WNT10A, SLC6A19, TPO, SLC5A5, DUOX2, DUOXA2, PAX8, HJV, HOGA1, TFR2, COL7A1, SLC39A4, ARL13B, FANCA , (...) View the complete list with 280 more genes Panel GTR000552567 complete gene list MPP3, FTCD, ADK, CTH, HAL, HGD, WNT10A, SLC6A19, TPO, SLC5A5, DUOX2, DUOXA2, PAX8, HJV, HOGA1, TFR2, COL7A1, SLC39A4, ARL13B, FANCA, F8, F9, JAK3, THRB, F11, PGK1, DNAH5, CHST6, CASQ2, TRDN, THOC2, IL1RAPL1, SLC16A2, BRWD3, RPS6KA3, FTSJ1, GDI1, USP9X, UPF3B, AFF2, HUWE1, PHF8, MVK, PEX10, NLGN4X, AP1S2, TPRN, TRIOBP, TMIE, PEX6, GJB3, TMC1, PRPS1, TMPRSS3, SLC4A11, STRC, POLR1C, OTOF, CUL4B, CASK, OPHN1, SYN1, KDM5C, PAK3, GRIA3, FGD1, IQSEC2, ATRX, MFSD8, PQBP1, DCX, POMT1, POMT2, TNNT1, SPART, L1CAM, BSND, COL4A4, CYP21A2, GNRHR, KCNJ11, DYSF, FKRP, CLCN1, AHI1, SPG11, ZFYVE26, GDAP1, MTMR2, SH3TC2, NDRG1, TMEM216, PKHD1, LAMC2, CLN5, CAPN3, TTPA, PEX1, MPL, MCOLN1, GRHPR, TH, UGT1A1, SLC26A2, SACS, SERPINA1, SGCB, SGCA, PEX7, PPT1, NPHS1, PROP1, CTNS, NEB, G6PD, FKTN, LAMB3, HBA1, CLN8, CLN6, NBN, ATM, SMN1, RMRP, POU3F4, PLP1, PLOD1, NPC2, NPC1, LIPA, LDLR, IDUA, IDS, GLA, GJB2, DMD, DHCR7, GBA, FANCC, CFTR, ARX, ASPA, ARSA, AR, AIRE, IL2RG, GNMT, ARSB, AHCY, AGA, ADA, ABCD4, NR2E3, SLC6A8, CYP17A1, CLN3, TPP1, ASL, BBS2, BBS1, BBS10, MKS1, PMM2, SLC25A20, SLC22A5, CYP27A1, ASS1, SLC3A1, LRPPRC, FXN, GALK1, GALE, GALT, GCDH, ETFDH, ETFA, ETFB, GBE1, ALDH4A1, IVD, GALC, SUCLG1, MLYCD, MAN2B1, DBT, MUT, MMAB, MCEE, SGSH, NAGLU, HGSNAT, GNS, GALNS, CPT1A, SURF1, AGXT, PAH, PTS, ACOX1, HEXB, HEXA, LMBRD1, MMADHC, ABCD1, ACSL4, OTC, RP2, AGPS, MYO7A, ETHE1, EYS, AMT, GLDC, PCCB, SPG7, CERKL, ACADSB, CTSD, TSFM, TUFM, HAX1, P3H1, SUCLA2, RDH12, CNGA1, G6PC, TAT, HMGCL, FAH, RS1, CNGB1, PDE6A, DHDDS, PDHB, ACSF3, IDH3B, CDH23, WHRN, SLC26A4, MECP2, CRB1, GUCY2D, RPE65, RPGR, TULP1, FH, HADHA, PANK2, SLC25A13, DLD, PCDH15, USH2A, CLRN1, CEP290, NPHP1, TMEM67, CNGB3, NDP, ABCA4, OCRL, GLB1, GNPTAB, CPT2, CPS1, MTRR, GPR143, TYR, SLC45A2, TYRP1, RAX, HBB, GAA, BCKDHB, BCKDHA, ATP7B, BTD, HLCS, ARG1, USH1C, PC, USH1G, ALDOB, AIPL1, ACAT1, ACADVL, AGL, ACADS, ACADM, CD40LG, LDLRAP1, PCBD1, SLC46A1, EVC2, ABCB11, MCCC2, MCCC1, MTHFR, FMR1, F5, F2 Specificity 1 % Genes 10 %
LEPRE1. By Fulgent Genetics Fulgent Genetics in United States. P3H1 Specificity 100 % Genes 10 %
P3H1. By Fulgent Genetics Fulgent Genetics in United States. P3H1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta type VIII. By Bioarray in Spain. P3H1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Sequencing LEPRE1 Gene. By Reference Laboratory Genetics in Spain. P3H1 Specificity 100 % Genes 10 %
CRTAP Sequence Analysis. By Baylor Miraca Genetics Laboratories in United States. CRTAP Specificity 100 % Genes 10 %
CRTAP Sequence Analysis (Familial Mutation/Variant Analysis). By Baylor Miraca Genetics Laboratories in United States. CRTAP Specificity 100 % Genes 10 %
CRTAP Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. CRTAP Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-CRTAP. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. CRTAP Specificity 100 % Genes 10 %
CRTAP. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain. CRTAP Specificity 100 % Genes 10 %
Osteogenesis imperfecta type VII (sequence analysis of CRTAP gene). By CGC Genetics in Portugal. CRTAP Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via CRTAP Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. CRTAP Specificity 100 % Genes 10 %
CRTAP-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. CRTAP Specificity 100 % Genes 10 %
Osteogenesis imperfecta type VII. By Centogene AG - the Rare Disease Company in Germany. CRTAP Specificity 100 % Genes 10 %
CRTAP mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. CRTAP Specificity 100 % Genes 10 %
Osteogenesis imperfecta: CRTAP gene sequence analysis. By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. CRTAP Specificity 100 % Genes 10 %
CRTAP. By Fulgent Genetics Fulgent Genetics in United States. CRTAP Specificity 100 % Genes 10 %
Osteogenesis Imperfecta type VII. By Bioarray in Spain. CRTAP Specificity 100 % Genes 10 %
Osteogenesis Imperfecta , Sequencing CRTAP Gene. By Reference Laboratory Genetics in Spain. CRTAP Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-SERPINH1. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. SERPINH1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta type X (sequence analysis of SERPINH1 gene). By CGC Genetics in Portugal. SERPINH1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via SERPINH1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. SERPINH1 Specificity 100 % Genes 10 %
SERPINH1-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. SERPINH1 Specificity 100 % Genes 10 %
Osteogenesis imperfecta, type 10. By Centogene AG - the Rare Disease Company in Germany. SERPINH1 Specificity 100 % Genes 10 %
SERPINH1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. SERPINH1 Specificity 100 % Genes 10 %
SERPINH1. By Fulgent Genetics Fulgent Genetics in United States. SERPINH1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via WNT1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. WNT1 Specificity 100 % Genes 10 %
WNT1-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. WNT1 Specificity 100 % Genes 10 %
Mental retardation - different panels. By Institute of Human Genetics Cologne University in Germany. EEF1B2, UBR7, PARP1, CAPN10, SLC31A1, TRMT1, PGAP2, GMPPA, TANGO2, IMPA1, RALGDS, ZBTB40, KCNK9, SETD1A, HERC2, TM4SF20, AHDC1, CCDC88A, ACBD6, KDM5A , (...) View the complete list with 847 more genes Panel GTR000558415 complete gene list EEF1B2, UBR7, PARP1, CAPN10, SLC31A1, TRMT1, PGAP2, GMPPA, TANGO2, IMPA1, RALGDS, ZBTB40, KCNK9, SETD1A, HERC2, TM4SF20, AHDC1, CCDC88A, ACBD6, KDM5A, WAC, CNKSR1, HIST3H3, ASCC3, GPT2, TMEM135, RABL6, SLC25A16, HIKESHI, ZCCHC8, INPP4A, GEMIN4, FRMD4A, CASP2, CKAP2L, PECR, PGAP3, MEIS2, KDM6B, CCNA2, KRBOX4, ADRA2B, SCAPER, SLC39A6, GON4L, HIST1H4B, HNRNPK, APC2, GTF2E2, RSPRY1, SFXN4, RMND1, ITPA, SNX27, FASN, PPP2R1A, GABBR2, TCF20, TRIP12, DCPS, MYT1L, MED13L, TRIO, ELP2, ISCA2, JAM3, KDM1A, DDX59, DARS, USP27X, KLHL15, RLIM, KCNH1, CAD, NECTIN1, UPB1, UNC80, SC5D, FAR1, MFF, RNF113A, SMOC1, MAB21L2, HMGB3, CLP1, FTO, ERCC1, TMCO1, STT3A, STT3B, AIMP1, UBE3B, SSR4, GPHN, RBM28, PIGT, SLC12A5, HDAC4, COLEC11, IGF1, KAT6A, DDX3X, POGZ, PEX11B, COL4A2, DHFR, FAM126A, PEPD, CA5A, GTF2H5, MPLKIP, AP1S1, BUB1B, ZSWIM6, PIGG, CHAMP1, WDR73, SNX14, APOPT1, PET100, POLR3B, POLR3A, WDR81, XPA, PMPCA, COQ4, ERCC5, SCYL1, PTRH2, LAMA1, COL18A1, CACNA1G, ACY1, BCAP31, KMT2B, CLPB, SERAC1, SLC1A4, PPP1R15B, TBCE, TUBGCP6, ASXL3, TUBGCP4, PYCR2, POC1A, LARP7, PLK4, GMNN, ORC1, TCF12, MEGF8, DPH1, CA8, CC2D1A, ANK3, CTCF, GATAD2B, ADAT3, CRADD, FBXO31, FMN2, KIF4A, METTL23, MID2, NDST1, SETD5, SLC6A17, TAF2, TTI2, ZMYND11, CEP63, CEP135, CDK6, CENPE, MFSD2A, MED17, SLC25A1, LAMB1, MPDZ, CCDC88C, PTDSS1, PDE4D, SNAP29, ASNS, KIF2A, KIF5C, TUBG1, KATNB1, CDK5, FRAS1, DNMT3B, ESCO2, RTTN, TBC1D20, CEP83, ZNF423, ZBTB20, TRMT10A, HEPACAM, TBC1D7, RNF125, KPTN, CSPP1, PDE6D, CEP104, KIAA0556, SRCAP, AFF4, PRMT7, IFT172, AGPAT2, KCNJ6, OCLN, UBR1, MICU1, TCTN3, PGM3, PACS1, PIK3R1, EPG5, PRKRA, GSS, TPI1, LIG4, ERCC8, AKT3, PIK3R2, B3GLCT, RARB, STIM1, RAB27A, MYO5A, DHCR24, EIF2AK3, SLC6A3, DDC, EARS2, MAT1A, TMEM165, COG5, COG6, ALG11, COG4, MT-TV, COX10, VLDLR, MYCN, RBBP8, IER3IP1, RAB18, PIK3CA, ARL13B, CPLANE1, CEP41, KIF7, RPGRIP1L, TCTN1, TCTN2, TMEM138, TMEM237, TTC21B, ERCC4, MASP1, AUTS2, KATNAL2, SATB2, SOX5, FANCD2, WNT1, GNAS, GNPAT, ASXL1, EFTUD2, RNASET2, EP300, THRB, DPP6, MT-CO3, MT-CO1, MT-ND5, MT-CO2, PGK1, CTDP1, KIF11, PRMT9, PPP2R5D, EXOSC2, FRY, RGS7, COL4A3BP, ADK, CCDC115, WDR45B, DIP2B, STAMBP, AP4M1, AP4E1, AP4B1, AP4S1, RAB3GAP2, ERLIN2, VPS37A, ADAR, TECPR2, DDHD2, CYP2U1, GBA2, TUBB4A, B4GALNT1, NT5C2, ENTPD1, PGAP1, IFIH1, MAG, HACE1, SMARCA2, ARID1A, SMARCB1, RRAS, RASA2, NSUN2, SPRED1, THOC2, CNKSR2, CCDC22, CLCN4, FRMPD4, EIF2S3, LAS1L, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, NAA10, SOX3, SLC16A2, TAF1, CLIC2, BRWD3, ZDHHC9, RAB40AL, RPL10, SHROOM4, RPS6KA3, FTSJ1, GDI1, ZC4H2, USP9X, UPF3B, UBE2A, TSPAN7, DLG3, DKC1, ZNF711, MAGT1, LAMP2, MBTPS2, AFF2, HCFC1, HUWE1, PHF8, CCBE1, NEU1, MVK, KAT6B, PEX5, PEX12, PEX10, PEX26, PEX13, KIAA0586, LZTR1, NLGN3, NLGN4X, CTNNB1, ARID1B, TMEM231, TBR1, HOXA1, CHD8, AP1S2, CACNA1C, EHMT1, FOXP1, LAMC3, MED12, MID1, ADNP, PTCHD1, FUCA1, NARS2, PEX6, PRPS1, MT-TS1, SOX10, DIAPH1, NLRP3, PNPT1, ERCC3, ERCC2, ATP6V1B2, ACTG1, ACTB, SALL1, SHANK2, SHANK3, ATP2A2, GFAP, VPS13B, TREX1, ZEB2, SETBP1, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, SYN1, KDM5C, PAK3, ARHGEF9, GRIA3, SYP, PHF6, FGD1, IQSEC2, ATRX, SMS, OFD1, KIF1BP, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, SAMHD1, PNKP, SPTAN1, PLCB1, ANKRD11, PIGV, PIGN, DYRK1A, GRIN1, NRXN1, PIGA, SCN8A, ROGDI, CRBN, GRIK2, MAN1B1, PRSS12, TRAPPC9, ZC3H14, ZNF526, CDH15, SOBP, C12orf57, LINS1, LRP2, MED23, TECR, KANSL1, ST3GAL3, WDR45, GNAO1, SZT2, NEXMIF, NR2F1, DOCK7, SLC13A5, KCNB1, PURA, SIK1, DNM1, KCNA2, EEF1A2, SPATA5, TBL1XR1, SETD2, CACNA2D2, KMT2D, ATP13A2, KCNT1, HCN1, GRIN2B, SLC6A1, SLC35A2, SCN2A, ST3GAL5, KCTD7, GABRB3, ATP1A3, ATP1A2, ASPM, MCPH1, B3GALNT2, LARGE1, CHKB, POMGNT2, DPM2, LAMA2, GRM1, SIL1, ANO10, ISPD, POMT1, POMT2, DAG1, TRAPPC11, VRK1, DYNC1H1, CCDC78, SPART, KIF1A, WASHC5, BSCL2, SLC33A1, L1CAM, KCNJ11, FGFR1, NF1, GCH1, ATXN10, FKRP, AHI1, SCN1A, SPG11, MT-ATP6, MT-TK, ZFYVE26, MT-TL1, NTRK1, FIG4, TMEM216, DPYD, PHGDH, CLN5, SLC17A5, SLC12A6, POMGNT1, PEX1, MCOLN1, TH, SLC35A3, PEX7, PPT1, FKTN, CLN8, CLN6, SMAD4, GPC3, PTCH1, NBN, NSD1, NIPBL, TSC1, SMC1A, SMC3, SYNGAP1, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, WDR62, SOS1, SLC2A1, SHOC2, RMRP, RAI1, PTPN11, PORCN, PLP1, PCDH19, NRAS, DMPK, MEF2C, MAP2K1, KRAS, IKBKG, IDUA, IDS, HRAS, GJC2, FOXG1, DMD, DHCR7, CREBBP, CHD7, CDKL5, BRAF, BLM, ARX, ASPA, FGFR3, PNP, MGME1, HPD, MOGS, DPAGT1, DOLK, AHCY, AGA, ABCD4, SDHA, PDHX, SLC6A8, FARS2, WWOX, PPOX, HESX1, CLN3, SMARCA4, KMT2A, SMARCE1, ARID2, ERCC6, SDCCAG8, WDPCP, BBIP1, IFT27, LZTFL1, GMPPB, POMK, FBXL4, EMC1, NKX2-1, SLC4A4, MAF, POC1B, MED25, AARS, DHTKD1, KDM6A, MAGEL2, ABCC9, GLI3, EZH2, NFIX, DNMT3A, ACVR1, SKI, TGFBR2, TGFBR1, DYM, NAGA, ATR, PCNT, CDK5RAP2, GLI2, CDON, CEP152, NALCN, ZIC2, TGIF1, TUBB2A, EXOSC3, MTOR, NECAP1, TPP1, SOX2, ASL, APTX, BBS2, BBS1, BBS4, BBS10, BBS9, MKS1, BBS12, BBS5, BBS7, PMM2, MGAT2, LRPPRC, GALE, GALT, CBS, L2HGDH, SLC25A15, MLYCD, MAN2B1, MANBA, DBT, CYB5R3, MUT, MMAA, NDUFAF5, NDUFS2, NDUFV1, NDUFS1, NDUFA11, NDUFA1, MOCS1, MOCS2, SGSH, NAGLU, HGSNAT, GNS, GUSB, NDUFS3, NDUFS7, NDUFS8, SURF1, COX15, CA2, ACOX1, SLC35C1, ALDH3A2, ALDH5A1, SUOX, ABHD5, MMADHC, ABCD1, BCOR, SLC9A6, ACSL4, MAOA, AIFM1, TIMM8A, GK, PDHA1, HCCS, PUS1, D2HGDH, ALG3, STRA6, ETHE1, MPI, ALG6, GAD1, SLC35A1, SCO2, AMT, GLDC, GCSH, B4GALT1, ALG12, COQ2, GRN, ALG2, ALG8, AP3B1, ALG1, ALG9, COG7, DPM1, MPDU1, SLC25A22, CTSD, DNAJC19, HAX1, TUSC3, DARS2, COG8, COG1, TUBA1A, MRPS22, RFT1, COQ8A, STXBP1, SDHB, AK1, GATM, GAMT, PGM1, DPM3, NUBPL, TAT, CCDC28B, ACSF3, DNM1L, ALDH18A1, DDOST, NDUFA12, ACO2, PDSS1, PDSS2, MECP2, SMPD1, FH, RAF1, PANK2, NDUFS4, DLD, SHH, TRIM32, TTC8, CEP290, MKKS, NPHP1, ARL6, TMEM67, NHS, HPRT1, OTX2, NDP, ELOVL4, OCRL, HSD17B10, SRD5A3, ATP6V0A2, PRODH, CC2D2A, PYCR1, MTRR, INPP5E, MTR, PAX6, PRKCG, MMACHC, ADSL, C12orf65, MFSD8, DNAJC5, CTSF, TUBB2B, STIL, ADGRG1, PAFAH1B1, FLNA, TUBA8, RELN, SIX3, RAB3GAP1, PQBP1, NDE1, QARS, EMX2, DCX, DEAF1, CENPJ, ARFGEF2, COL4A1, PIGO, BRAT1, PRRT2, DEPDC5, PRIMA1, TBC1D24, ASAH1, ALG13, MBD5, GRIN2A, GABRA1, CHD2, KCNQ3, KCNQ2, BCS1L, BCKDHB, BCKDHA, B4GALT7, AUH, ATP7A, HLCS, ANKH, PC, ACAD9, MCCC2, MCCC1, PTEN, UBE3A, FMR1 Specificity 1 % Genes 10 %
Ataxia and differential diagnoses Panel. By CeGaT GmbH in Germany. RPIA, POLH, NOP56, XPC, VWA3B, CWF19L1, WDR73, TMEM240, SNX14, CHCHD10, RNF170, POLR3B, POLR3A, WDR81, XPA, TRNT1, PMPCA, RUBCN, SLC9A1, STUB1 , (...) View the complete list with 184 more genes Panel GTR000522481 complete gene list RPIA, POLH, NOP56, XPC, VWA3B, CWF19L1, WDR73, TMEM240, SNX14, CHCHD10, RNF170, POLR3B, POLR3A, WDR81, XPA, TRNT1, PMPCA, RUBCN, SLC9A1, STUB1, ERCC5, SCYL1, RNF216, RNASEH1, ELOVL5, PTRH2, DMXL2, PCNA, PIK3R5, GRID2, LAMA1, SLC52A2, ATCAY, BEAN1, CACNA1G, ATP2B3, ATP8A2, RARS, UBA5, COX20, CA8, CCDC88C, DNAJC3, MARS2, VLDLR, ARL13B, RPGRIP1L, ERCC4, CP, WNT1, GBA2, UCHL1, KIF1C, ERCC6, GMPPB, NKX2-1, NALCN, CLCN2, NEU1, PEX10, PRPS1, DNMT1, POLR1C, ERCC3, ERCC2, GFAP, KCNJ10, PNKP, SNAP25, KCNA2, DNAJC5, CTSF, ADGRG1, TSEN54, RELN, PRRT2, LMNB2, EPM2A, KCNC1, HCN1, FOLR1, SLC6A1, SCN2A, SLC19A3, PRICKLE1, NHLRC1, GOSR2, ATP1A3, SPTBN2, TTBK2, TGM6, FGF14, PDYN, ITPR1, KCNC3, KCND3, EEF2, VAMP1, GRM1, SIL1, TDP1, ANO10, SYT14, SLC1A3, CACNB4, KCNA1, TRAPPC11, SYNE1, VRK1, SETX, PNPLA6, BSCL2, ATN1, TBP, CACNA1A, ATXN7, ATXN10, ATXN3, ATXN2, PPP2R2B, AHI1, CSTB, EIF2B4, EIF2B2, EIF2B3, GJB1, TMEM216, PLA2G6, EIF2B5, CLN5, TTPA, SLC17A5, SACS, PEX7, PEX2, MTTP, CLN6, MRE11, ATM, ATXN1, NPC2, NPC1, EIF2B1, GBA, ARSA, PDHX, WWOX, TPP1, APTX, PMM2, CYP27A1, FASTKD2, FXN, GCDH, L2HGDH, GALC, DLAT, NAGLU, NDUFS7, PHYH, HEXB, ALDH5A1, HEXA, ABCB7, ALG6, SPG7, COQ2, PDP1, FLVCR1, DNAJC19, TSFM, DARS2, COQ8A, SPR, NUBPL, MTPAP, TTC19, ACO2, PDSS1, PDSS2, COQ9, OPA3, AFG3L2, POLG, CEP290, NPHP1, TMEM67, ELOVL4, CC2D2A, GLB1, WFS1, OPA1, AMACR, INPP5E, PAX6, PRKCG, TWNK, AUH, ATP7B, BTD, UQCRQ, ABHD12, AARS2, FMR1 Specificity 1 % Genes 10 %
WNT1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. WNT1 Specificity 100 % Genes 10 %
WNT1. By Fulgent Genetics Fulgent Genetics in United States. WNT1 Specificity 100 % Genes 10 %
CNS Tumor Gene Set. By Genomics and Pathology Services Washington University in St. Louis in United States. H3F3A, KLF4, TRAF7, HIST1H3B, DAXX, FUBP1, MYB, MYBL1, CIC, MYC, SMO, MN1, ERBB2, NTRK2, PIK3R1, AKT1, IDH1, PDGFRA, EGFR, PIK3CA , (...) View the complete list with 28 more genes Panel GTR000522547 complete gene list H3F3A, KLF4, TRAF7, HIST1H3B, DAXX, FUBP1, MYB, MYBL1, CIC, MYC, SMO, MN1, ERBB2, NTRK2, PIK3R1, AKT1, IDH1, PDGFRA, EGFR, PIK3CA, WNT1, SMARCB1, SMARCA4, TERT, DNMT3A, NOTCH1, MTOR, CTNNB1, MED12, ATRX, SETD2, FGFR1, NF1, NTRK1, MET, CDKN2A, SUFU, NF2, PTCH1, FGFR2, KRAS, BRAF, IDH2, SHH, RB1, WT1, TP53, PTEN Specificity 3 % Genes 10 %
Osteogenesis Imperfecta Type XV , Sequencing WNT1 Gene. By Reference Laboratory Genetics in Spain. WNT1 Specificity 100 % Genes 10 %
SERPINF1 Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1 Sequence Analysis. By Baylor Miraca Genetics Laboratories in United States. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1 Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories in United States. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1 Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories in United States. SERPINF1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta, autosomal recessive-SERPINF1. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom. SERPINF1 Specificity 100 % Genes 10 %
Osteogenesis Imperfecta via SERPINF1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics in United States. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1-related osteogenesis imperfecta. By Institute of Human Genetics Cologne University in Germany. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1 mutational analysis. By Connective Tissue Laboratory Ghent University Hospital in Belgium. SERPINF1 Specificity 100 % Genes 10 %
SERPINF1. By Fulgent Genetics Fulgent Genetics in United States. SERPINF1 Specificity 100 % Genes 10 %

Alternate names

Osteogenesis Imperfecta, Type Iii; Oi3 Is also known as oi, type iii, osteogenesis imperfecta, progressively deforming, with normal sclerae;oi type 3; progressive deforming osteogenesis imperfecta; severe osteogenesis imperfecta.

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