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Test Catalog ( 15 Results )
  • Custom Arrhythmia Panel *

    Test Code: 695C
    Genes: ABCC9, AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, DES, DSC2, DSG2, DSP, GPD1L, HCN4, HERG, JUP, KCND3, KCNE1, KCNE1L, KCNE2, KCNE3, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LMNA, NKX2-5, PKP2, PLN, RANGRF, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SNTA1, TGFB3, TMEM43, TRDN, TRPM4, TTN
    Disorders: Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Long QT Syndrome (LQTS), Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Short QT Syndrome (SQTS), Brugada Syndrome (BrS)

  • Custom ARVC Panel *

    Test Code: 483C
    Genes: DES, DSC2, DSG2, DSP, JUP, LMNA, PKP2, PLN, RYR2, SCN5A, TGFB3, TMEM43, TTN
    Disorders: Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

  • Custom Brugada Syndrome (BrS) Panel *

    Test Code: 481C
    Genes: ABCC9, CACNA1C, CACNB2, GPD1L, KCND3, KCNE3, KCNJ8, PKP2, SCN10A, SCN1B, SCN2B, SCN3B, SCN5A, TRPM4
    Disorders: Brugada Syndrome (BrS)

  • Custom Cardiology Panel *

    Test Code: J779
    Genes:
    Disorders: Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Cutis Laxa, Autosomal Dominant, Danon Disease, Dilated Cardiomyopathy (DCM), Ehlers-Danlos Syndrome, Fabry Disease, Familial Hypercholesterolemia, Homocystinuria due to Cystathionine Beta-Synthase Deficiency, Hypertrophic Cardiomyopathy (HCM), Left Ventricular Noncompaction (LVNC), Loeys-Dietz syndrome (LDS), Long QT Syndrome (LQTS), Marfan Syndrome/LDS/Related Disorders, Noonan Syndrome, Occipital Horn Disease, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Arterial Tortuosity syndrome, Short QT Syndrome (SQTS), Stickler syndrome, Sudden Cardiac Arrest, Sudden Unexplained Death, Thoracic Aortic Aneurysm and Dissection (TAAD) and Related Disorders, Transthyretin Amyloidosis, Wolff-Parkinson-White Syndrome, Brittle Cornea syndrome, Brugada Syndrome (BrS)

  • Custom Cardiomyopathy Panel *

    Test Code: 694C
    Genes: ABCC9, ACTC1, ACTN2, ALMS1, ALPK3, ANKRD1, BAG3, BRAF, CAV3, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, FHL1, FKRP, FKTN, GATAD1, GLA, HCN4, HRAS, ILK, JPH2, JUP, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MIB1, MTND1, MTND5, MTND6, MTTD, MTTG, MTTH, MTTI, MTTK, MTTL1, MTTL2, MTTM, MTTQ, MTTS1, MTTS2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NKX2-5, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN5A, SGCD, SOS1, TAZ, TCAP, TGFB3, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, TXNRD2, VCL
    Disorders: Dilated Cardiomyopathy (DCM), Hypertrophic Cardiomyopathy (HCM), Left Ventricular Noncompaction (LVNC), Noonan Syndrome, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

  • Custom Combined Cardiac Panel *

    Test Code: 935C
    Genes: ABCC9, ACTC1, ACTN2, AKAP9, ALMS1, ALPK3, ANK2, ANKRD1, BAG3, BRAF, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, FHL1, FKRP, FKTN, GATAD1, GLA, GPD1L, HCN4, HERG, HRAS, ILK, JPH2, JUP, KCND3, KCNE1, KCNE1L, KCNE2, KCNE3, KCNJ2, KCNJ5, KCNJ8, KCNQ1, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MIB1, MTND1, MTND5, MTND6, MTTD, MTTG, MTTH, MTTI, MTTK, MTTL1, MTTL2, MTTM, MTTQ, MTTS1, MTTS2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NKX2-5, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PTPN11, RAF1, RANGRF, RBM20, RIT1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SGCD, SNTA1, SOS1, TAZ, TCAP, TGFB3, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, TXNRD2, VCL
    Disorders: Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Dilated Cardiomyopathy (DCM), Hypertrophic Cardiomyopathy (HCM), Left Ventricular Noncompaction (LVNC), Long QT Syndrome (LQTS), Noonan Syndrome, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Short QT Syndrome (SQTS), Sudden Cardiac Arrest, Brugada Syndrome (BrS)

  • Custom CPVT Panel *

    Test Code: 482C
    Genes: CALM1, CALM2, CALM3, CASQ2, KCNJ2, RYR2, TRDN
    Disorders: Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

  • Custom DCM/LVNC Panel *

    Test Code: J554C
    Genes: ABCC9, ACTC1, ACTN2, ALMS1, ANKRD1, BAG3, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, FKTN, GATAD1, ILK, LAMA4, LAMP2, LDB3, LMNA, MIB1, MTND1, MTND5, MTND6, MTTD, MTTH, MTTI, MTTK, MTTL1, MTTL2, MTTM, MTTQ, MTTS1, MTTS2, MYBPC3, MYH6, MYH7, MYPN, NEBL, NEXN, PLN, PRDM16, RAF1, RBM20, SCN5A, SGCD, TAZ, TCAP, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, TXNRD2, VCL
    Disorders: Danon Disease, Dilated Cardiomyopathy (DCM), Left Ventricular Noncompaction (LVNC), Transthyretin Amyloidosis

  • Custom Familial Hypercholesterolemia (FH) Panel *

    Test Code: J556C
    Genes: APOB, LDLR, LDLRAP1, PCSK9
    Disorders: Familial Hypercholesterolemia

  • Custom HCM Panel *

    Test Code: J553C
    Genes: ACTC1, ACTN2, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, MTTG, MTTI, MTTK, MTTQ, MYBPC3, MYH7, MYL2, MYL3, PLN, PRKAG2, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTR, VCL
    Disorders: Danon Disease, Fabry Disease, Hypertrophic Cardiomyopathy (HCM), Transthyretin Amyloidosis, Wolff-Parkinson-White Syndrome

  • Custom HDCT Panel *

    Test Code: J555C
    Genes: ACTA2, ADAMTS2, ALDH18A1, ATP6V0A2, ATP7A, B3GALT6, B4GALT7, CBS, CHST14, COL11A1, COL11A2, COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A2, COL9A1, COL9A2, DSE, EFEMP2, ELN, FBLN5, FBN1, FBN2, FKBP14, FLNA, LTBP4, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, PLOD1, PRDM5, PRKG1, PYCR1, RIN2, SKI, SLC2A10, SLC39A13, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2, ZNF469
    Disorders: Congenital Contractural Arachnodactyly, Cutis Laxa, Autosomal Dominant, Ehlers-Danlos Syndrome, Homocystinuria due to Cystathionine Beta-Synthase Deficiency, Loeys-Dietz syndrome (LDS), Marfan Syndrome/LDS/Related Disorders, Occipital Horn Disease, Arterial Tortuosity syndrome, Shprintzen-Goldberg syndrome, Stickler syndrome, Thoracic Aortic Aneurysm and Dissection (TAAD) and Related Disorders, Brittle Cornea syndrome

  • Custom LQTS Panel *

    Test Code: 727C
    Genes: AKAP9, ANK2, CACNA1C, CALM1, CALM2, CALM3, CAV3, HERG, KCNE1, KCNE2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1, TRDN
    Disorders: Long QT Syndrome (LQTS)

  • Custom Marfan/TAAD & Related Disorders Panel *

    Test Code: 883C
    Genes: ACTA2, CBS, COL3A1, COL5A1, COL5A2, FBN1, FBN2, FLNA, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, PRKG1, SKI, SLC2A10, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2
    Disorders: Marfan Syndrome/LDS/Related Disorders, Thoracic Aortic Aneurysm and Dissection (TAAD) and Related Disorders

  • Custom SCA Arrhythmia Panel *

    Test Code: J552C
    Genes: ANK2, CALM1, CALM2, CALM3, CASQ2, CAV3, HERG, KCNE1, KCNE2, KCNJ2, KCNQ1, RYR2, SCN5A
    Disorders: Sudden Cardiac Arrest, Sudden Unexplained Death

  • Custom SQTS Panel *

    Test Code: J551C
    Genes: CACNA1C, CACNB2, HERG, KCNJ2, KCNQ1
    Disorders: Short QT Syndrome (SQTS)