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ATP13A2

Exames relacionados Estratégia de Análise Gene relacionado
Parkinsonismo de Início Precoce Painel por Sequenciamento de Próxima Geração ABCD1, APP, ARSA, ATP13A2, ATP1A3, ATP7B, CHMP2B, CSF1R, CYP27A1, DCTN1, DNAJC6, EIF4G1, FBXO7, FUS, GALC, GBA, GCHI, GFAP, GLA, GRN, HEXA, HTRA2, ITM2B, LMNB1, LRRK2, MAPT, NOTCH3, NPC1, NPC2, PANK2, PARK7, PINK1, PLA2G6, PNKD, POLG, PPT1, PRKN, PRKRA, PRNP, PRRT2, PSAP, PSEN1, PSEN2, SGCE, SLC2A1, SLC6A3, SNCA, SPG11, SPR, SQSTM1, TARDBP, TH, THAP1, TOR1A, TREM2, TYROBP, UBQLN2, UCHL1, VCP, VPS35
Distonias e Neuroferritinopatias (NBIA) Painel por Sequenciamento de Próxima Geração ANO3, ATP1A3, GCH1, GNAL, PARK2, PNKD, PRKRA, PRRT2, SGCE, SLC2A1, SLC6A3, SPR, TH, THAP1, TOR1A, TUBB4A, ATP13A2, C19ORF12, COASY, CP, CRAT, DCAF17, FA2H, FTL, GTPBP2, IBA57, PANK2, PLA2G6, REPS1, WDR45
Demências Painel por Sequenciamento de Próxima Geração ABCD1, APP, ARSA, ATP13A2, ATP1A3, ATP7B, CHMP2B, CSF1R, CYP27A1, DCTN1, DNAJC6, EIF4G1, FBXO7, FUS, GALC, GBA, GCH1, GFAP, GLA, GRN, HEXA, HTRA2, ITM2B, LMNB1, LRRK2, MAPT, NOTCH3, NPC1, NPC2, PANK2, PARK2, PARK7, PINK1, PLA2G6, PNKD, POLG, PPT1, PRKRA, PRNP, PRRT2, PSAP, PSEN1, PSEN2, SGCE, SLC2A1, SLC6A3, SNCA, SPG11, SPR, SQSTM1, TARDBP, TH, THAP1, TOR1A, TREM2, TYROBP, UBQLN2, UCHL1, VCP, VPS35
Paraplegia Espástica Painel por Sequenciamento de Próxima Geração ALDH18A1, AMPD2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ARL6IP1, ATL1, ATP13A2, B4GALNT1, BSCL2, C12ORF65, C19ORF12, CAPN1, CCT5, CPT1C, CYP2U1, CYP7B1, DDHD1, DDHD2, DSTYK, ENTPD1, ERLIN1, ERLIN2, FA2H, FARS2, GBA2, GJC2, HACE1, HSPD1, IBA57, KIF1A, KIF5A, KLC2, L1CAM, MAG, NIPA1, NT5C2, PLP1, PNPLA6, REEP1, REEP2, RTN2, SLC33A1, SPAST, SPG11, SPG20, SPG7, TECPR2, TFG, UCHL1, VPS37A, WASHC5, ZFYVE26, ZFYVE27, BICD2, SOX10, KLC4
tipo 6, Parkinson Análise de Deleção/Duplicação ATP13A2, GCH1, LRRK2, PARK2, PARK7, PINK1, SNCA, UCHL1
Parkinson tipo 9 Sequenciamento Completo do Gene ATP13A2
Parkinson Hereditario Painel por Sequenciamento de Próxima Geração A2M, AAAS, ACE, ACMSD, ADH1C, APOE, APP, ATP13A2, ATP1A3, ATXN2, CHCHD2, CSF1R, DCTN1, DJ1, DNAJC6, DNMT1, EIF4G1, FBXO7, GBA, GCH1, GIGYF2, GLUD2, GRN, HTRA2, LRRK2, MAPT, MPO, PARK2, PARK7, PINK1, PLA2G6, PRKAG2, PRKRA, PRNP, PSEN1, PSEN2, SLC30A10, SLC6A3, SNCA, SNCB, SYNJ1, TAF1, TBP, TH, TREM2, TYROBP, UCHL1, VPS13C, VPS35
Malformações Cerebrais / Transtorno de Migração Neuronal, Painel Expandido Painel por Sequenciamento de Próxima Geração ACTB, ACTG1, ADAR, ADGRG1, AFF2, AGTR2, AKT1, AKT3, ALDH7A1, AP1S2, ARFGEF2, ARHGEF15, ARHGEF6, ARX, ASAH1, ASPA, ASPM, ATP13A2, ATP6AP2, BRWD3, C19ORF12, CACNA1H, CACNB4, CASK, CASR, CCND2, CDK5, CDK5RAP2, CDKL5, CDON, CECR1, CENPJ, CEP152, CHD2, CHD8, CHRNA2, CHRNA4, CHRNB2, CLCN4, CLN3, CLN5, CLN6, CLP1, CNTNAP2, COL4A1, COL4A2, CP, CSTB, CUL4B, CYP27A1, DARS, DCAF17, DCX, DEPDC5, DIS3L2, DISP1, DKC1, DLG3, DLL1, DOK7, DYRK1A, EEF1A2, EFHC1, EIF2B3, EIF2B5, EIF2S3, EMX2, EOMES, EPM2A, EXOSC3, EZH2, FA2H, FGD1, FGF8, FGFR3, FLNA, FOXG1, FOXH1, FTL, FTSJ1, GABRA1, GABRD, GABRG2, GALC, GAMT, GAS1, GDI1, GK, GLDC, GLI2, GLI3, GNAQ, GOSR2, GPC3, GPSM2, GRIA3, GRIN2A, HCFC1, HCN1, HDAC8, HEPACAM, HERC2, HGSNAT, HNRNPDL, HPRT1, HSD17B10, HTRA1, HUWE1, IDS, IFIH1, IGBP1, IKBKAP, IL1RAPL1, IQSEC2, ITM2B, JAM3, KATNB1, KCNH5, KCNQ2, KCNQ3, KCNT1, KCTD7, KDM5C, KIAA2022, KIF1BP, KIF2A, KIF5C, KIF7, KLF8, KPTN, L1CAM, LAMB1, LGI1, MAGT1, MAOA, MBD5, MBTPS2, MCPH1, MECP2, MED12, MEF2C, MID1, MLC1, MYBPC1, NAA10, NDE1
Lipofuscinose Ceróide Neuronal Infantil Painel por Sequenciamento de Próxima Geração ATP13A2, CLN3, CLN5, CLN6, CLN8, CTSD, CTSF, DNAJC5, GRN, KCTD7, MFSD8, PPT1, TPP1
Distonia, Isolada Painel por Sequenciamento de Próxima Geração ATP13A2, ATP1A3, GCH1, PLA2G6, PRKRA, SLC30A10, SLC6A3, SPR, TAF1, TH
Neurodegeneração com Acúmulo de Ferro no Cérebro Painel por Sequenciamento de Próxima Geração ATP13A2, C19ORF12, COASY, CP, CRAT, DCAF17, FA2H, FTL, GTPBP2, IBA57, PANK2, PLA2G6, REPS1, SCP2, WDR45
Encefalopatias (Mitocondrial/Epiléptico) Painel por Sequenciamento de Próxima Geração AARS2, ABCB7, ABCD1, ABHD5, ACAD9, ACADM, ACADS, ACADVL, ACOX1, ACTG2, ADAR, ADCK3, ADCK4, AFG3L2, AGK, AGL, AGRN, AIFM1, AIMP1, ALAS2, ALDH3A2, ALDH7A1, ALG14, ALG2, AMACR, ANO10, APOPT1, APTX, ARG1, ARHGEF15, ARHGEF9, ARSA, ARX, ASAH1, ASPA, ATP13A2, ATP1A2, ATP1A3, ATP5A1, ATP5E, ATP7B, ATPAF2, AUH, BCS1L, BOLA3, C10ORF2, C12ORF65, C19ORF12, CACNA1A, CACNA1H, CACNB4, CAD, CARS2, CASR, CCDC115, CDKL5, CHAT, CHCHD10, CHD2, CHD8, CHKB, CHRNA1, CHRNA2, CHRNA4, CHRNB1, CHRNB2, CHRND, CHRNE, CLCN4, CLN3, CLN5, CLN6, CLP1, CLPB, CLPP, COL4A1, COL4A2, COLQ, COQ2, COQ4, COQ6, COQ7, COQ9, COX10, COX14, COX15, COX4I2, COX6B1, COX8A, CP, CPT1A, CPT2, CSF1R, CSTB, CYP27A1, DARS2, DCAF17, DEPDC5, DGUOK, DLAT, DLD, DNA2, DNAJC19, DNAJC3, DNM2, DOCK7, DOK7, DPAGT1, DPM2, DYRK1A, EARS2, ECHS1, EEF1A2, EFHC1, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EPG5, EPM2A, ETFA, ETFB, ETFDH, ETHE1, EXOSC8, FA2H, FAM126A, FARS2, FASTKD2, FBXL4, FDX2, FLAD1, FOLR1, FOXG1, FOXRED1, FTL, FUCA1, GABRA1, GABRD, GABRG2, GALC, GAMT
Distonia, Discinesia Painel por Sequenciamento de Próxima Geração ACY1, ADCY5, ANO3, ATM, ATP13A2, ATP1A3, CACNA1B, CIZ1, COL6A3, DLAT, GCDH, GCH1, GNAL, HPCA, KCNMA1, KCTD17, MR1, PDHA1, PDHX, PLA2G6, PNKD, PRKRA, PRRT2, RELN, SCN8A, SGCE, SLC16A2, SLC2A1, SLC30A10, SLC6A3, SPR, SUCLA2, TAF1, TH, THAP1, TOR1A, TUBB4A
Distonia, Responsiva a Dopa e/ou Parkinsonismo Painel por Sequenciamento de Próxima Geração ATP13A2, ATP1A3, GCH1, PLA2G6, PRKRA, SLC30A10, SLC6A3, SPR, TAF1, TH
Subscrever ATP13A2