NeoPainel para Miocardiopatias

Investigação genética de Miocardiopatias por NeoPainel, com análise direcionada baseada em exoma.

Aplicações

Doenças raras e hereditárias

Amostras aceitas

Sangue periférico (preferencial), Swab bucal, DNA extraído

Prazo estimado

Tradicional · 30 dias corridos, após a confirmação do pedido Rápido · 15 dias corridos, após a confirmação do pedido

Método-base

Exoma

Escopo analítico

Análise dos genes listados conforme a base exômica e os critérios técnicos validados pelo laboratório.

Genes analisados

347 genes analisados.

Ver conteúdo completo +

AARS2, ABCC6, ABCC9, ACAD9, ACADVL, ACTA1, ACTC1, ACTN2, ADCY5, AGK, AGL, AGPAT2, AHCY, ALG1, ALG12, ALMS1, ALPK3, ANK2, ANKRD1, ANKS6, ARSB, ATAD3A, ATP5F1E, ATPAF2, BAG3, BCS1L, BMP2, BOLA3, BRAF, BSCL2, C1QBP, C1QTNF5, CACNA1C, CACNB2, CALM1, CALM2, CALM3, CALR3, CAP2, CASQ2, CAV3, CAVIN1, CBL, CDH2, CENPE, CEP19, CHKB, CLIC2, CLN3, CNBP, COA5, COA6, COA8, COQ2, COQ4, COX10, COX14, COX15, COX20, COX6B1, COX7B, CPT1A, CPT2, CRYAB, CSRP3, CTNNA3, D2HGDH, DCAF8, DES, DLD, DMD, DMPK, DNAJC19, DNM1L, DOLK, DPM3, DPP6, DSC2, DSG2, DSP, DTNA, ECHS1, ELAC2, EMD, EPG5, ERBB3, EYA4, FAH, FASTKD2, FBXL4, FBXO32, FHL1, FHOD3, FIG4, FKRP, FKTN, FLAD1, FLNC, FNIP1, FOXRED1, FTO, FUCA1, FXN, GAA, GATA6, GATAD1, GBE1, GJA5, GLA, GLB1, GMPPB, GNAI2, GNB5, GNPTAB, GNS, GPC3, GPD1L, GSN, GTPBP3, GYG1, GYS1, HADH, HADHA, HADHB, HCCS, HCN4, HFE, HGSNAT, HPS1, HRAS, HSD17B10, IDH2, IDUA, ITPA, JPH2, JUP, KAT6B, KCNA5, KCND3, KCNE2, KCNE3, KCNH1, KCNH2, KCNJ2, KCNJ5, KCNQ1, KIF20A, KLF10, KLHL24, KRAS, LAMA2, LAMA4, LAMP2, LDB3, LIAS, LMNA, LMOD2, LZTR1, MAP2K1, MAP2K2, MCCC2, MCM10, MGME1, MIB1, MLYCD, MMUT, MRAS, MRPL3, MRPL44, MRPS22, MRPS7, MTFMT, MTO1, MT-TI, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYL4, MYLK2, MYLK3, MYO6, MYOT, MYOZ2, MYPN, NAGLU, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA6, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFB10, NDUFB11, NDUFB3, NDUFB8, NDUFB9, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NEBL, NEU1, NEXN, NF1, NKX2-5, NONO, NPPA, NRAP, NRAS, NUBPL, NUP155, PAM16, PCCA, PCCB, PDLIM3, PET100, PGM1, PHYH, PIGT, PKP2, PLEKHM2, PLN, PMM2, PNPLA2, POLG, POMT1, PPA2, PPCS, PPP1CB, PPP1R13L, PRDM16, PRG4, PRKAG2, PRKAR1A, PSEN1, PSEN2, PSMB4, PSMB8, PSMB9, PTPN11, QRSL1, RAB3GAP2, RAF1, RASA1, RBCK1, RBM20, RIT1, RMND1, RPL3L, RPSA, RRAGD, RRAS, RYR2, SCN1B, SCN2B, SCN3B, SCN5A, SCO1, SCO2, SDHA, SDHAF1, SDHD, SELENON, SGCA, SGCB, SGCD, SGCG, SGSH, SHMT2, SHOC2, SLC19A2, SLC22A5, SLC25A20, SLC25A26, SLC25A3, SLC25A4, SLC30A5, SLC6A6, SOD2, SOS1, SOS2, SPEG, SPRED1, SURF1, SYNE1, SYNE2, TACO1, TAF1A, TAFAZZIN, TANGO2, TAPT1, TBX1, TBX20, TBX3, TBX5, TCAP, TECRL, TFR2, TGFB3, TIMMDC1, TMEM126A, TMEM126B, TMEM43, TMEM70, TMPO, TNNC1, TNNI3, TNNI3K, TNNT2, TOP3A, TOR1AIP1, TPM1, TPM3, TRDN, TRIM63, TRIT1, TRMT5, TRNT1, TRPM7, TSC1, TSFM, TTN, TTR, TWNK, TXNRD2, UBR1, UQCRFS1, VCL, VPS33A, WFS1, XPNPEP3, YARS2, YWHAE

Solicitação médica

Necessária