{"count":220263,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2178","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2176","results":[{"created":"2019-11-17T17:24:59.390341+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN5A was added\ngene: SCN5A was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN5A was set to Unknown","entity_name":"SCN5A","entity_type":"gene"},{"created":"2019-11-17T17:24:59.301644+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN4B was added\ngene: SCN4B was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN4B was set to Unknown","entity_name":"SCN4B","entity_type":"gene"},{"created":"2019-11-17T17:24:59.217141+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNQ1 was added\ngene: KCNQ1 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNQ1 was set to Unknown","entity_name":"KCNQ1","entity_type":"gene"},{"created":"2019-11-17T17:24:59.129364+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNJ5 was added\ngene: KCNJ5 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ5 was set to Unknown","entity_name":"KCNJ5","entity_type":"gene"},{"created":"2019-11-17T17:24:59.043559+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNJ2 was added\ngene: KCNJ2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ2 was set to Unknown","entity_name":"KCNJ2","entity_type":"gene"},{"created":"2019-11-17T17:24:58.949778+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNH2 was added\ngene: KCNH2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNH2 was set to Unknown","entity_name":"KCNH2","entity_type":"gene"},{"created":"2019-11-17T17:24:58.853870+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNE2 was added\ngene: KCNE2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNE2 was set to Unknown","entity_name":"KCNE2","entity_type":"gene"},{"created":"2019-11-17T17:24:58.756246+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNE1 was added\ngene: KCNE1 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNE1 was set to Unknown","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-11-17T17:24:58.638119+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CAV3 was added\ngene: CAV3 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAV3 was set to Unknown","entity_name":"CAV3","entity_type":"gene"},{"created":"2019-11-17T17:24:58.528678+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CACNA1C was added\ngene: CACNA1C was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNA1C was set to Unknown","entity_name":"CACNA1C","entity_type":"gene"},{"created":"2019-11-17T17:24:58.424429+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ANK2 was added\ngene: ANK2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ANK2 was set to Unknown","entity_name":"ANK2","entity_type":"gene"},{"created":"2019-11-17T17:24:58.317216+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AKAP9 was added\ngene: AKAP9 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AKAP9 was set to Unknown","entity_name":"AKAP9","entity_type":"gene"},{"created":"2019-11-17T17:24:58.247126+11:00","panel_name":"Long QT syndrome_VCGS","panel_id":131,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Long QT syndrome_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T17:24:46.624572+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZMPSTE24 was added\ngene: ZMPSTE24 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZMPSTE24 was set to Unknown","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2019-11-17T17:24:46.545118+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WRN was added\ngene: WRN was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WRN was set to Unknown","entity_name":"WRN","entity_type":"gene"},{"created":"2019-11-17T17:24:46.472000+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPRTN was added\ngene: SPRTN was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPRTN was set to Unknown","entity_name":"SPRTN","entity_type":"gene"},{"created":"2019-11-17T17:24:46.398567+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PSMB8 was added\ngene: PSMB8 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PSMB8 was set to Unknown","entity_name":"PSMB8","entity_type":"gene"},{"created":"2019-11-17T17:24:46.320557+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PPARG was added\ngene: PPARG was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PPARG was set to Unknown","entity_name":"PPARG","entity_type":"gene"},{"created":"2019-11-17T17:24:46.248019+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: POLD1 was added\ngene: POLD1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: POLD1 was set to Unknown","entity_name":"POLD1","entity_type":"gene"},{"created":"2019-11-17T17:24:46.174970+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PLIN1 was added\ngene: PLIN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PLIN1 was set to Unknown","entity_name":"PLIN1","entity_type":"gene"},{"created":"2019-11-17T17:24:46.101106+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIK3R1 was added\ngene: PIK3R1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PIK3R1 was set to Unknown","entity_name":"PIK3R1","entity_type":"gene"},{"created":"2019-11-17T17:24:46.030203+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PCYT1A was added\ngene: PCYT1A was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PCYT1A was set to Unknown","entity_name":"PCYT1A","entity_type":"gene"},{"created":"2019-11-17T17:24:45.957831+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LMNB2 was added\ngene: LMNB2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LMNB2 was set to Unknown","entity_name":"LMNB2","entity_type":"gene"},{"created":"2019-11-17T17:24:45.883880+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LMNA was added\ngene: LMNA was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LMNA was set to Unknown","entity_name":"LMNA","entity_type":"gene"},{"created":"2019-11-17T17:24:45.809858+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LIPE was added\ngene: LIPE was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LIPE was set to Unknown","entity_name":"LIPE","entity_type":"gene"},{"created":"2019-11-17T17:24:45.738148+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNJ6 was added\ngene: KCNJ6 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ6 was set to Unknown","entity_name":"KCNJ6","entity_type":"gene"},{"created":"2019-11-17T17:24:45.668093+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FBN1 was added\ngene: FBN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FBN1 was set to Unknown","entity_name":"FBN1","entity_type":"gene"},{"created":"2019-11-17T17:24:45.595665+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ERCC8 was added\ngene: ERCC8 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ERCC8 was set to Unknown","entity_name":"ERCC8","entity_type":"gene"},{"created":"2019-11-17T17:24:45.521423+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ERCC6 was added\ngene: ERCC6 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ERCC6 was set to Unknown","entity_name":"ERCC6","entity_type":"gene"},{"created":"2019-11-17T17:24:45.445164+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CIDEC was added\ngene: CIDEC was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CIDEC was set to Unknown","entity_name":"CIDEC","entity_type":"gene"},{"created":"2019-11-17T17:24:45.377863+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CAVIN1 was added\ngene: CAVIN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAVIN1 was set to Unknown","entity_name":"CAVIN1","entity_type":"gene"},{"created":"2019-11-17T17:24:45.308005+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CAV1 was added\ngene: CAV1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAV1 was set to Unknown","entity_name":"CAV1","entity_type":"gene"},{"created":"2019-11-17T17:24:45.229671+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BSCL2 was added\ngene: BSCL2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BSCL2 was set to Unknown","entity_name":"BSCL2","entity_type":"gene"},{"created":"2019-11-17T17:24:44.964609+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BLM was added\ngene: BLM was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BLM was set to Unknown","entity_name":"BLM","entity_type":"gene"},{"created":"2019-11-17T17:24:44.896810+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BANF1 was added\ngene: BANF1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BANF1 was set to Unknown","entity_name":"BANF1","entity_type":"gene"},{"created":"2019-11-17T17:24:44.830599+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AKT2 was added\ngene: AKT2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AKT2 was set to Unknown","entity_name":"AKT2","entity_type":"gene"},{"created":"2019-11-17T17:24:44.752771+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AGPAT2 was added\ngene: AGPAT2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AGPAT2 was set to Unknown","entity_name":"AGPAT2","entity_type":"gene"},{"created":"2019-11-17T17:24:44.708647+11:00","panel_name":"Lipodystrophy / Lipoatrophy_VCGS","panel_id":130,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Lipodystrophy / Lipoatrophy_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T17:24:24.285026+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZIC4 was added\ngene: ZIC4 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZIC4 was set to Unknown","entity_name":"ZIC4","entity_type":"gene"},{"created":"2019-11-17T17:24:24.212201+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZIC1 was added\ngene: ZIC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZIC1 was set to Unknown","entity_name":"ZIC1","entity_type":"gene"},{"created":"2019-11-17T17:24:24.139314+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNT1 was added\ngene: WNT1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WNT1 was set to Unknown","entity_name":"WNT1","entity_type":"gene"},{"created":"2019-11-17T17:24:24.004532+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR81 was added\ngene: WDR81 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR81 was set to Unknown","entity_name":"WDR81","entity_type":"gene"},{"created":"2019-11-17T17:24:23.925628+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VLDLR was added\ngene: VLDLR was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VLDLR was set to Unknown","entity_name":"VLDLR","entity_type":"gene"},{"created":"2019-11-17T17:24:23.852573+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC21B was added\ngene: TTC21B was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TTC21B was set to Unknown","entity_name":"TTC21B","entity_type":"gene"},{"created":"2019-11-17T17:24:23.778650+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM67 was added\ngene: TMEM67 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM67 was set to Unknown","entity_name":"TMEM67","entity_type":"gene"},{"created":"2019-11-17T17:24:23.700235+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM237 was added\ngene: TMEM237 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM237 was set to Unknown","entity_name":"TMEM237","entity_type":"gene"},{"created":"2019-11-17T17:24:23.624030+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM231 was added\ngene: TMEM231 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM231 was set to Unknown","entity_name":"TMEM231","entity_type":"gene"},{"created":"2019-11-17T17:24:23.552289+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM216 was added\ngene: TMEM216 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM216 was set to Unknown","entity_name":"TMEM216","entity_type":"gene"},{"created":"2019-11-17T17:24:23.475478+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM138 was added\ngene: TMEM138 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM138 was set to Unknown","entity_name":"TMEM138","entity_type":"gene"},{"created":"2019-11-17T17:24:23.397248+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN3 was added\ngene: TCTN3 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN3 was set to Unknown","entity_name":"TCTN3","entity_type":"gene"},{"created":"2019-11-17T17:24:23.327894+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN2 was added\ngene: TCTN2 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN2 was set to Unknown","entity_name":"TCTN2","entity_type":"gene"},{"created":"2019-11-17T17:24:23.258877+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN1 was added\ngene: TCTN1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN1 was set to Unknown","entity_name":"TCTN1","entity_type":"gene"},{"created":"2019-11-17T17:24:23.187841+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SUFU was added\ngene: SUFU was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SUFU was set to Unknown","entity_name":"SUFU","entity_type":"gene"},{"created":"2019-11-17T17:24:23.106921+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPGRIP1L was added\ngene: RPGRIP1L was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RPGRIP1L was set to Unknown","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2019-11-17T17:24:23.018163+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PDE6D was added\ngene: PDE6D was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PDE6D was set to Unknown","entity_name":"PDE6D","entity_type":"gene"},{"created":"2019-11-17T17:24:22.947920+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: OFD1 was added\ngene: OFD1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OFD1 was set to Unknown","entity_name":"OFD1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.872885+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NPHP3 was added\ngene: NPHP3 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NPHP3 was set to Unknown","entity_name":"NPHP3","entity_type":"gene"},{"created":"2019-11-17T17:24:22.795363+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NPHP1 was added\ngene: NPHP1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NPHP1 was set to Unknown","entity_name":"NPHP1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.724392+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NID1 was added\ngene: NID1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NID1 was set to Unknown","entity_name":"NID1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.649071+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MKS1 was added\ngene: MKS1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MKS1 was set to Unknown","entity_name":"MKS1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.575740+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LAMC1 was added\ngene: LAMC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LAMC1 was set to Unknown","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.503070+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KIF7 was added\ngene: KIF7 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIF7 was set to Unknown","entity_name":"KIF7","entity_type":"gene"},{"created":"2019-11-17T17:24:22.432513+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: INPP5E was added\ngene: INPP5E was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: INPP5E was set to Unknown","entity_name":"INPP5E","entity_type":"gene"},{"created":"2019-11-17T17:24:22.359662+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FOXC1 was added\ngene: FOXC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FOXC1 was set to Unknown","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.289504+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CSPP1 was added\ngene: CSPP1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CSPP1 was set to Unknown","entity_name":"CSPP1","entity_type":"gene"},{"created":"2019-11-17T17:24:22.216723+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C5orf42 was added\ngene: C5orf42 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: C5orf42 was set to Unknown","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-11-17T17:24:22.145584+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CEP41 was added\ngene: CEP41 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP41 was set to Unknown","entity_name":"CEP41","entity_type":"gene"},{"created":"2019-11-17T17:24:22.076142+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CEP290 was added\ngene: CEP290 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP290 was set to Unknown","entity_name":"CEP290","entity_type":"gene"},{"created":"2019-11-17T17:24:22.006591+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CC2D2A was added\ngene: CC2D2A was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CC2D2A was set to Unknown","entity_name":"CC2D2A","entity_type":"gene"},{"created":"2019-11-17T17:24:21.933101+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: B9D2 was added\ngene: B9D2 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: B9D2 was set to Unknown","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-11-17T17:24:21.864734+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: B9D1 was added\ngene: B9D1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: B9D1 was set to Unknown","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-11-17T17:24:21.793951+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ARMC8 was added\ngene: ARMC8 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ARMC8 was set to Unknown","entity_name":"ARMC8","entity_type":"gene"},{"created":"2019-11-17T17:24:21.717927+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ARL13B was added\ngene: ARL13B was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ARL13B was set to Unknown","entity_name":"ARL13B","entity_type":"gene"},{"created":"2019-11-17T17:24:21.642217+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AHI1 was added\ngene: AHI1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AHI1 was set to Unknown","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-17T17:24:21.598958+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Joubert syndrome and other cerebellar malformations_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T17:22:07.729814+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: XK was added\ngene: XK was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: XK was set to Unknown","entity_name":"XK","entity_type":"gene"},{"created":"2019-11-17T17:22:07.634363+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WT1 was added\ngene: WT1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WT1 was set to Unknown","entity_name":"WT1","entity_type":"gene"},{"created":"2019-11-17T17:22:07.543515+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS13A was added\ngene: VPS13A was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VPS13A was set to Unknown","entity_name":"VPS13A","entity_type":"gene"},{"created":"2019-11-17T17:22:07.458788+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VHL was added\ngene: VHL was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VHL was set to Unknown","entity_name":"VHL","entity_type":"gene"},{"created":"2019-11-17T17:22:07.372530+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VCP was added\ngene: VCP was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VCP was set to Unknown","entity_name":"VCP","entity_type":"gene"},{"created":"2019-11-17T17:22:07.285437+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VAPB was added\ngene: VAPB was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VAPB was set to Unknown","entity_name":"VAPB","entity_type":"gene"},{"created":"2019-11-17T17:22:07.196346+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UCHL1 was added\ngene: UCHL1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: UCHL1 was set to Unknown","entity_name":"UCHL1","entity_type":"gene"},{"created":"2019-11-17T17:22:07.096909+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBQLN2 was added\ngene: UBQLN2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: UBQLN2 was set to Unknown","entity_name":"UBQLN2","entity_type":"gene"},{"created":"2019-11-17T17:22:07.000207+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA4A was added\ngene: TUBA4A was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBA4A was set to Unknown","entity_name":"TUBA4A","entity_type":"gene"},{"created":"2019-11-17T17:22:06.915129+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTN was added\ngene: TTN was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TTN was set to Unknown","entity_name":"TTN","entity_type":"gene"},{"created":"2019-11-17T17:22:06.831066+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSC2 was added\ngene: TSC2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSC2 was set to Unknown","entity_name":"TSC2","entity_type":"gene"},{"created":"2019-11-17T17:22:06.746232+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSC1 was added\ngene: TSC1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSC1 was set to Unknown","entity_name":"TSC1","entity_type":"gene"},{"created":"2019-11-17T17:22:06.658282+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TPM1 was added\ngene: TPM1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TPM1 was set to Unknown","entity_name":"TPM1","entity_type":"gene"},{"created":"2019-11-17T17:22:06.564942+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TP53 was added\ngene: TP53 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TP53 was set to Unknown","entity_name":"TP53","entity_type":"gene"},{"created":"2019-11-17T17:22:06.467989+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNT2 was added\ngene: TNNT2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TNNT2 was set to Unknown","entity_name":"TNNT2","entity_type":"gene"},{"created":"2019-11-17T17:22:06.365392+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNI3 was added\ngene: TNNI3 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TNNI3 was set to Unknown","entity_name":"TNNI3","entity_type":"gene"},{"created":"2019-11-17T17:22:06.276995+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM43 was added\ngene: TMEM43 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM43 was set to Unknown","entity_name":"TMEM43","entity_type":"gene"},{"created":"2019-11-17T17:22:06.185433+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TH was added\ngene: TH was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TH was set to Unknown","entity_name":"TH","entity_type":"gene"},{"created":"2019-11-17T17:22:05.987464+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR2 was added\ngene: TGFBR2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TGFBR2 was set to Unknown","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2019-11-17T17:22:05.897856+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR1 was added\ngene: TGFBR1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TGFBR1 was set to Unknown","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2019-11-17T17:22:05.803392+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TARDBP was added\ngene: TARDBP was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TARDBP was set to Unknown","entity_name":"TARDBP","entity_type":"gene"},{"created":"2019-11-17T17:22:05.718144+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STK11 was added\ngene: STK11 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STK11 was set to Unknown","entity_name":"STK11","entity_type":"gene"},{"created":"2019-11-17T17:22:05.624793+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPG11 was added\ngene: SPG11 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPG11 was set to Unknown","entity_name":"SPG11","entity_type":"gene"},{"created":"2019-11-17T17:22:05.529922+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPART was added\ngene: SPART was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPART was set to Unknown","entity_name":"SPART","entity_type":"gene"},{"created":"2019-11-17T17:22:05.441622+11:00","panel_name":"Incidentalome_VCGS","panel_id":126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SORL1 was added\ngene: SORL1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SORL1 was set to Unknown","entity_name":"SORL1","entity_type":"gene"}]}