{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2201","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2199","results":[{"created":"2019-11-17T16:17:54.688197+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HES7 was added\ngene: HES7 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HES7 was set to Unknown","entity_name":"HES7","entity_type":"gene"},{"created":"2019-11-17T16:17:54.608959+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GNPAT was added\ngene: GNPAT was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GNPAT was set to Unknown","entity_name":"GNPAT","entity_type":"gene"},{"created":"2019-11-17T16:17:54.532216+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GLI3 was added\ngene: GLI3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GLI3 was set to Unknown","entity_name":"GLI3","entity_type":"gene"},{"created":"2019-11-17T16:17:54.453083+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GDF5 was added\ngene: GDF5 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GDF5 was set to Unknown","entity_name":"GDF5","entity_type":"gene"},{"created":"2019-11-17T16:17:54.376177+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FLNB was added\ngene: FLNB was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FLNB was set to Unknown","entity_name":"FLNB","entity_type":"gene"},{"created":"2019-11-17T16:17:54.297336+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FLNA was added\ngene: FLNA was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FLNA was set to Unknown","entity_name":"FLNA","entity_type":"gene"},{"created":"2019-11-17T16:17:54.220886+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FKBP10 was added\ngene: FKBP10 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FKBP10 was set to Unknown","entity_name":"FKBP10","entity_type":"gene"},{"created":"2019-11-17T16:17:54.140013+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGFR3 was added\ngene: FGFR3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FGFR3 was set to Unknown","entity_name":"FGFR3","entity_type":"gene"},{"created":"2019-11-17T16:17:54.007127+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGFR2 was added\ngene: FGFR2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FGFR2 was set to Unknown","entity_name":"FGFR2","entity_type":"gene"},{"created":"2019-11-17T16:17:53.931922+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FAM20C was added\ngene: FAM20C was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FAM20C was set to Unknown","entity_name":"FAM20C","entity_type":"gene"},{"created":"2019-11-17T16:17:53.857499+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FAM111A was added\ngene: FAM111A was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FAM111A was set to Unknown","entity_name":"FAM111A","entity_type":"gene"},{"created":"2019-11-17T16:17:53.784009+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EVC2 was added\ngene: EVC2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EVC2 was set to Unknown","entity_name":"EVC2","entity_type":"gene"},{"created":"2019-11-17T16:17:53.710981+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EVC was added\ngene: EVC was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EVC was set to Unknown","entity_name":"EVC","entity_type":"gene"},{"created":"2019-11-17T16:17:53.637218+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EBP was added\ngene: EBP was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EBP was set to Unknown","entity_name":"EBP","entity_type":"gene"},{"created":"2019-11-17T16:17:53.562380+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DYNC2LI1 was added\ngene: DYNC2LI1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DYNC2LI1 was set to Unknown","entity_name":"DYNC2LI1","entity_type":"gene"},{"created":"2019-11-17T16:17:53.487913+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DYNC2H1 was added\ngene: DYNC2H1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DYNC2H1 was set to Unknown","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2019-11-17T16:17:53.413332+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DLL3 was added\ngene: DLL3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DLL3 was set to Unknown","entity_name":"DLL3","entity_type":"gene"},{"created":"2019-11-17T16:17:53.338776+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DHCR7 was added\ngene: DHCR7 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DHCR7 was set to Unknown","entity_name":"DHCR7","entity_type":"gene"},{"created":"2019-11-17T16:17:53.263615+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DDR2 was added\ngene: DDR2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DDR2 was set to Unknown","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-17T16:17:53.187965+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CSPP1 was added\ngene: CSPP1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CSPP1 was set to Unknown","entity_name":"CSPP1","entity_type":"gene"},{"created":"2019-11-17T16:17:53.110854+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CRTAP was added\ngene: CRTAP was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CRTAP was set to Unknown","entity_name":"CRTAP","entity_type":"gene"},{"created":"2019-11-17T16:17:53.037158+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CREB3L1 was added\ngene: CREB3L1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CREB3L1 was set to Unknown","entity_name":"CREB3L1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.963895+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL2A1 was added\ngene: COL2A1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL2A1 was set to Unknown","entity_name":"COL2A1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.890518+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL1A2 was added\ngene: COL1A2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL1A2 was set to Unknown","entity_name":"COL1A2","entity_type":"gene"},{"created":"2019-11-17T16:17:52.817770+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL1A1 was added\ngene: COL1A1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL1A1 was set to Unknown","entity_name":"COL1A1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.745388+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL11A2 was added\ngene: COL11A2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL11A2 was set to Unknown","entity_name":"COL11A2","entity_type":"gene"},{"created":"2019-11-17T16:17:52.672585+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL11A1 was added\ngene: COL11A1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL11A1 was set to Unknown","entity_name":"COL11A1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.599493+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C21orf2 was added\ngene: C21orf2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: C21orf2 was set to Unknown","entity_name":"C21orf2","entity_type":"gene"},{"created":"2019-11-17T16:17:52.526997+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CEP120 was added\ngene: CEP120 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP120 was set to Unknown","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-11-17T16:17:52.454310+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CANT1 was added\ngene: CANT1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CANT1 was set to Unknown","entity_name":"CANT1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.382431+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C2CD3 was added\ngene: C2CD3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: C2CD3 was set to Unknown","entity_name":"C2CD3","entity_type":"gene"},{"created":"2019-11-17T16:17:52.310306+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BMPER was added\ngene: BMPER was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BMPER was set to Unknown","entity_name":"BMPER","entity_type":"gene"},{"created":"2019-11-17T16:17:52.238472+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BMP1 was added\ngene: BMP1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BMP1 was set to Unknown","entity_name":"BMP1","entity_type":"gene"},{"created":"2019-11-17T16:17:52.165354+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ARSE was added\ngene: ARSE was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ARSE was set to Unknown","entity_name":"ARSE","entity_type":"gene"},{"created":"2019-11-17T16:17:52.088734+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ALPL was added\ngene: ALPL was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ALPL was set to Unknown","entity_name":"ALPL","entity_type":"gene"},{"created":"2019-11-17T16:17:52.014655+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AGPS was added\ngene: AGPS was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AGPS was set to Unknown","entity_name":"AGPS","entity_type":"gene"},{"created":"2019-11-17T16:17:51.967446+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:15:12.435738+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: XPR1 was added\ngene: XPR1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: XPR1 was set to Unknown","entity_name":"XPR1","entity_type":"gene"},{"created":"2019-11-17T16:15:12.351536+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR45 was added\ngene: WDR45 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: WDR45 was set to Unknown","entity_name":"WDR45","entity_type":"gene"},{"created":"2019-11-17T16:15:12.269952+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS35 was added\ngene: VPS35 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: VPS35 was set to Unknown","entity_name":"VPS35","entity_type":"gene"},{"created":"2019-11-17T16:15:12.188466+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS13A was added\ngene: VPS13A was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: VPS13A was set to Unknown","entity_name":"VPS13A","entity_type":"gene"},{"created":"2019-11-17T16:15:12.103777+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TWNK was added\ngene: TWNK was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TWNK was set to Unknown","entity_name":"TWNK","entity_type":"gene"},{"created":"2019-11-17T16:15:11.960964+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB4A was added\ngene: TUBB4A was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TUBB4A was set to Unknown","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2019-11-17T16:15:11.878541+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TH was added\ngene: TH was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TH was set to Unknown","entity_name":"TH","entity_type":"gene"},{"created":"2019-11-17T16:15:11.795135+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TAF1 was added\ngene: TAF1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TAF1 was set to Unknown","entity_name":"TAF1","entity_type":"gene"},{"created":"2019-11-17T16:15:11.710190+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SYNJ1 was added\ngene: SYNJ1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SYNJ1 was set to Unknown","entity_name":"SYNJ1","entity_type":"gene"},{"created":"2019-11-17T16:15:11.628180+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPR was added\ngene: SPR was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SPR was set to Unknown","entity_name":"SPR","entity_type":"gene"},{"created":"2019-11-17T16:15:11.546453+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPG11 was added\ngene: SPG11 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SPG11 was set to Unknown","entity_name":"SPG11","entity_type":"gene"},{"created":"2019-11-17T16:15:11.458287+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SNCA was added\ngene: SNCA was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SNCA was set to Unknown","entity_name":"SNCA","entity_type":"gene"},{"created":"2019-11-17T16:15:11.368775+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC6A3 was added\ngene: SLC6A3 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SLC6A3 was set to Unknown","entity_name":"SLC6A3","entity_type":"gene"},{"created":"2019-11-17T16:15:11.282870+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC39A14 was added\ngene: SLC39A14 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SLC39A14 was set to Unknown","entity_name":"SLC39A14","entity_type":"gene"},{"created":"2019-11-17T16:15:11.200774+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC30A10 was added\ngene: SLC30A10 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SLC30A10 was set to Unknown","entity_name":"SLC30A10","entity_type":"gene"},{"created":"2019-11-17T16:15:11.116638+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC20A2 was added\ngene: SLC20A2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: SLC20A2 was set to Unknown","entity_name":"SLC20A2","entity_type":"gene"},{"created":"2019-11-17T16:15:11.032230+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RAB39B was added\ngene: RAB39B was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: RAB39B was set to Unknown","entity_name":"RAB39B","entity_type":"gene"},{"created":"2019-11-17T16:15:10.946395+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PTS was added\ngene: PTS was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PTS was set to Unknown","entity_name":"PTS","entity_type":"gene"},{"created":"2019-11-17T16:15:10.863043+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PSEN1 was added\ngene: PSEN1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PSEN1 was set to Unknown","entity_name":"PSEN1","entity_type":"gene"},{"created":"2019-11-17T16:15:10.776369+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRNP was added\ngene: PRNP was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PRNP was set to Unknown","entity_name":"PRNP","entity_type":"gene"},{"created":"2019-11-17T16:15:10.695855+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRKRA was added\ngene: PRKRA was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PRKRA was set to Unknown","entity_name":"PRKRA","entity_type":"gene"},{"created":"2019-11-17T16:15:10.614264+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRKN was added\ngene: PRKN was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PRKN was set to Unknown","entity_name":"PRKN","entity_type":"gene"},{"created":"2019-11-17T16:15:10.532967+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: POLG was added\ngene: POLG was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: POLG was set to Unknown","entity_name":"POLG","entity_type":"gene"},{"created":"2019-11-17T16:15:10.450357+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PLA2G6 was added\ngene: PLA2G6 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PLA2G6 was set to Unknown","entity_name":"PLA2G6","entity_type":"gene"},{"created":"2019-11-17T16:15:10.363338+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PINK1 was added\ngene: PINK1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PINK1 was set to Unknown","entity_name":"PINK1","entity_type":"gene"},{"created":"2019-11-17T16:15:10.283945+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PDGFRB was added\ngene: PDGFRB was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PDGFRB was set to Unknown","entity_name":"PDGFRB","entity_type":"gene"},{"created":"2019-11-17T16:15:10.202995+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PDGFB was added\ngene: PDGFB was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PDGFB was set to Unknown","entity_name":"PDGFB","entity_type":"gene"},{"created":"2019-11-17T16:15:10.118355+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PARK7 was added\ngene: PARK7 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PARK7 was set to Unknown","entity_name":"PARK7","entity_type":"gene"},{"created":"2019-11-17T16:15:09.990216+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PANK2 was added\ngene: PANK2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: PANK2 was set to Unknown","entity_name":"PANK2","entity_type":"gene"},{"created":"2019-11-17T16:15:09.907092+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: OPA3 was added\ngene: OPA3 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: OPA3 was set to Unknown","entity_name":"OPA3","entity_type":"gene"},{"created":"2019-11-17T16:15:09.821394+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MECP2 was added\ngene: MECP2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: MECP2 was set to Unknown","entity_name":"MECP2","entity_type":"gene"},{"created":"2019-11-17T16:15:09.740122+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MAPT was added\ngene: MAPT was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: MAPT was set to Unknown","entity_name":"MAPT","entity_type":"gene"},{"created":"2019-11-17T16:15:09.660751+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LYST was added\ngene: LYST was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: LYST was set to Unknown","entity_name":"LYST","entity_type":"gene"},{"created":"2019-11-17T16:15:09.580580+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LRRK2 was added\ngene: LRRK2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: LRRK2 was set to Unknown","entity_name":"LRRK2","entity_type":"gene"},{"created":"2019-11-17T16:15:09.500575+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KIF5A was added\ngene: KIF5A was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: KIF5A was set to Unknown","entity_name":"KIF5A","entity_type":"gene"},{"created":"2019-11-17T16:15:09.416788+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HTT was added\ngene: HTT was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: HTT was set to Unknown","entity_name":"HTT","entity_type":"gene"},{"created":"2019-11-17T16:15:09.335570+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GRN was added\ngene: GRN was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: GRN was set to Unknown","entity_name":"GRN","entity_type":"gene"},{"created":"2019-11-17T16:15:09.255526+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GCH1 was added\ngene: GCH1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: GCH1 was set to Unknown","entity_name":"GCH1","entity_type":"gene"},{"created":"2019-11-17T16:15:09.172275+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FTL was added\ngene: FTL was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: FTL was set to Unknown","entity_name":"FTL","entity_type":"gene"},{"created":"2019-11-17T16:15:09.088860+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FMR1 was added\ngene: FMR1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: FMR1 was set to Unknown","entity_name":"FMR1","entity_type":"gene"},{"created":"2019-11-17T16:15:08.951814+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FBXO7 was added\ngene: FBXO7 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: FBXO7 was set to Unknown","entity_name":"FBXO7","entity_type":"gene"},{"created":"2019-11-17T16:15:08.874298+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJC6 was added\ngene: DNAJC6 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: DNAJC6 was set to Unknown","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-11-17T16:15:08.794317+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJC5 was added\ngene: DNAJC5 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: DNAJC5 was set to Unknown","entity_name":"DNAJC5","entity_type":"gene"},{"created":"2019-11-17T16:15:08.715135+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DCTN1 was added\ngene: DCTN1 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: DCTN1 was set to Unknown","entity_name":"DCTN1","entity_type":"gene"},{"created":"2019-11-17T16:15:08.638469+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DCAF17 was added\ngene: DCAF17 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: DCAF17 was set to Unknown","entity_name":"DCAF17","entity_type":"gene"},{"created":"2019-11-17T16:15:08.560678+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CSF1R was added\ngene: CSF1R was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: CSF1R was set to Unknown","entity_name":"CSF1R","entity_type":"gene"},{"created":"2019-11-17T16:15:08.480973+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CP was added\ngene: CP was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: CP was set to Unknown","entity_name":"CP","entity_type":"gene"},{"created":"2019-11-17T16:15:08.403030+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COASY was added\ngene: COASY was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: COASY was set to Unknown","entity_name":"COASY","entity_type":"gene"},{"created":"2019-11-17T16:15:08.321692+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLN3 was added\ngene: CLN3 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: CLN3 was set to Unknown","entity_name":"CLN3","entity_type":"gene"},{"created":"2019-11-17T16:15:08.242378+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C9orf72 was added\ngene: C9orf72 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: C9orf72 was set to Unknown","entity_name":"C9orf72","entity_type":"gene"},{"created":"2019-11-17T16:15:08.164244+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C19orf12 was added\ngene: C19orf12 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: C19orf12 was set to Unknown","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-11-17T16:15:08.086641+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP1A3 was added\ngene: ATP1A3 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: ATP1A3 was set to Unknown","entity_name":"ATP1A3","entity_type":"gene"},{"created":"2019-11-17T16:15:08.006560+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP13A2 was added\ngene: ATP13A2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: ATP13A2 was set to Unknown","entity_name":"ATP13A2","entity_type":"gene"},{"created":"2019-11-17T16:15:07.925911+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: APP was added\ngene: APP was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: APP was set to Unknown","entity_name":"APP","entity_type":"gene"},{"created":"2019-11-17T16:15:07.845732+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AFG3L2 was added\ngene: AFG3L2 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: AFG3L2 was set to Unknown","entity_name":"AFG3L2","entity_type":"gene"},{"created":"2019-11-17T16:15:07.792691+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Early onset Parkinson disease_MelbourneGenomics_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:14:27.599360+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VRK1 was added\ngene: VRK1 was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: VRK1 was set to Unknown","entity_name":"VRK1","entity_type":"gene"},{"created":"2019-11-17T16:14:27.516674+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VCP was added\ngene: VCP was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: VCP was set to Unknown","entity_name":"VCP","entity_type":"gene"},{"created":"2019-11-17T16:14:27.434231+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VAPB was added\ngene: VAPB was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: VAPB was set to Unknown","entity_name":"VAPB","entity_type":"gene"},{"created":"2019-11-17T16:14:27.352752+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBQLN2 was added\ngene: UBQLN2 was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: UBQLN2 was set to Unknown","entity_name":"UBQLN2","entity_type":"gene"},{"created":"2019-11-17T16:14:27.270685+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBA1 was added\ngene: UBA1 was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: UBA1 was set to Unknown","entity_name":"UBA1","entity_type":"gene"},{"created":"2019-11-17T16:14:27.189244+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA4A was added\ngene: TUBA4A was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TUBA4A was set to Unknown","entity_name":"TUBA4A","entity_type":"gene"},{"created":"2019-11-17T16:14:27.104337+11:00","panel_name":"Motor neuron disease MND_MelbourneGenomics_VCGS","panel_id":25,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPV4 was added\ngene: TRPV4 was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship\nMode of inheritance for gene: TRPV4 was set to Unknown","entity_name":"TRPV4","entity_type":"gene"}]}