Parkinson Disease, NGS
Genetic diagnosis of Parkinson’s disease; inform treatment decisions and familial risk.
Genelist (116): ADAMTS13, ADH1C, ADORA1, AFG3L2, APOA1BP, APOE, APP, ATP13A2, ATP1A3, ATP6AP2, ATP7B, ATXN2, ATXN3, C19orf12, C19ORF12, CHCHD10, CHCHD2, CLN3, COASY, COMT, CP, CSF1R, CYP27A1, CYP2D6, DCAF17, DCTN1, DDC, DNAJB2, DNAJC12, DNAJC13, DNAJC5, DNAJC6, DNM1L, EIF4G1, ERCC8, FBXO7, FMR1, FTL, FUS, GBA1, GBA2, GCH1, GET3, GIGYF2, GLUD2, GRN, HTRA2, JAM2, KIF1C, KIF5A, LRP10, LRRK2, LYST, MAPT, MCCC1, MECP2, MICU1, MPV17, MYORG, NOTCH3, NPC1, NPC2, NUS1, PANK2, PARK7, PDE10A, PDE8B, PDGFB, PDGFRB, PEX1, PINK1, PITX3, PLA2G6, PODXL, POLG, POLG2, PRKAR1B, PRKN, PRKRA, PRNP, PSEN1, PSEN2, PTEN, PTRHD1, PTS, QDPR, RAB29, RAB39B, SLC20A2, SLC30A10, SLC39A14, SLC6A3, SMPD1, SNCA, SNCB, SNORD118, SPG11, SPR, STX1B, SYNJ1, TAF1, TARDBP, TBP, TENM4, TH, TMEM230, TRPM7, TWNK, UBTF, UCHL1, VPS13A, VPS13C, VPS35, WDR45, XPR1, ZFYVE26
Featured Review
Genetic diagnosis of Parkinson’s disease; inform treatment decisions and familial risk.
Genelist (116): ADAMTS13, ADH1C, ADORA1, AFG3L2, APOA1BP, APOE, APP, ATP13A2, ATP1A3, ATP6AP2, ATP7B, ATXN2, ATXN3, C19orf12, C19ORF12, CHCHD10, CHCHD2, CLN3, COASY, COMT, CP, CSF1R, CYP27A1, CYP2D6, DCAF17, DCTN1, DDC, DNAJB2, DNAJC12, DNAJC13, DNAJC5, DNAJC6, DNM1L, EIF4G1, ERCC8, FBXO7, FMR1, FTL, FUS, GBA1, GBA2, GCH1, GET3, GIGYF2, GLUD2, GRN, HTRA2, JAM2, KIF1C, KIF5A, LRP10, LRRK2, LYST, MAPT, MCCC1, MECP2, MICU1, MPV17, MYORG, NOTCH3, NPC1, NPC2, NUS1, PANK2, PARK7, PDE10A, PDE8B, PDGFB, PDGFRB, PEX1, PINK1, PITX3, PLA2G6, PODXL, POLG, POLG2, PRKAR1B, PRKN, PRKRA, PRNP, PSEN1, PSEN2, PTEN, PTRHD1, PTS, QDPR, RAB29, RAB39B, SLC20A2, SLC30A10, SLC39A14, SLC6A3, SMPD1, SNCA, SNCB, SNORD118, SPG11, SPR, STX1B, SYNJ1, TAF1, TARDBP, TBP, TENM4, TH, TMEM230, TRPM7, TWNK, UBTF, UCHL1, VPS13A, VPS13C, VPS35, WDR45, XPR1, ZFYVE26