{"count":220437,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1509","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1507","results":[{"created":"2020-11-09T16:41:59.296106+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BRAF was added\ngene: BRAF was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRAF was set to Unknown","entity_name":"BRAF","entity_type":"gene"},{"created":"2020-11-09T16:41:59.254948+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BMPR1A was added\ngene: BMPR1A was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BMPR1A was set to Unknown","entity_name":"BMPR1A","entity_type":"gene"},{"created":"2020-11-09T16:41:59.212580+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BIRC3 was added\ngene: BIRC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BIRC3 was set to Unknown","entity_name":"BIRC3","entity_type":"gene"},{"created":"2020-11-09T16:41:59.170669+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BCR was added\ngene: BCR was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCR was set to Unknown","entity_name":"BCR","entity_type":"gene"},{"created":"2020-11-09T16:41:59.129155+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BCL6 was added\ngene: BCL6 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCL6 was set to Unknown","entity_name":"BCL6","entity_type":"gene"},{"created":"2020-11-09T16:41:59.086882+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BCL2 was added\ngene: BCL2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCL2 was set to Unknown","entity_name":"BCL2","entity_type":"gene"},{"created":"2020-11-09T16:41:59.045563+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BAP1 was added\ngene: BAP1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BAP1 was set to Unknown","entity_name":"BAP1","entity_type":"gene"},{"created":"2020-11-09T16:41:59.003473+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATM was added\ngene: ATM was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ATM was set to Unknown","entity_name":"ATM","entity_type":"gene"},{"created":"2020-11-09T16:41:58.963234+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ARL11 was added\ngene: ARL11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ARL11 was set to Unknown","entity_name":"ARL11","entity_type":"gene"},{"created":"2020-11-09T16:41:58.922630+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: APC was added\ngene: APC was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: APC was set to Unknown","entity_name":"APC","entity_type":"gene"},{"created":"2020-11-09T16:41:58.880911+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ABL1 was added\ngene: ABL1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ABL1 was set to Unknown","entity_name":"ABL1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.828823+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CACNA1S was added\ngene: CACNA1S was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CACNA1S was set to Unknown","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2020-11-09T16:41:58.785820+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RYR1 was added\ngene: RYR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RYR1 was set to Unknown","entity_name":"RYR1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.738804+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR1 was added\ngene: TGFBR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TGFBR1 was set to Unknown","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.697311+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMAD3 was added\ngene: SMAD3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SMAD3 was set to Unknown","entity_name":"SMAD3","entity_type":"gene"},{"created":"2020-11-09T16:41:58.656471+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYH11 was added\ngene: MYH11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYH11 was set to Unknown","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-11-09T16:41:58.613270+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FBN1 was added\ngene: FBN1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: FBN1 was set to Unknown","entity_name":"FBN1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.574238+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL3A1 was added\ngene: COL3A1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: COL3A1 was set to Unknown","entity_name":"COL3A1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.534512+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ACTA2 was added\ngene: ACTA2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ACTA2 was set to Unknown","entity_name":"ACTA2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.495329+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TPM1 was added\ngene: TPM1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TPM1 was set to Unknown","entity_name":"TPM1","entity_type":"gene"},{"created":"2020-11-09T16:41:58.456036+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNT2 was added\ngene: TNNT2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TNNT2 was set to Unknown","entity_name":"TNNT2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.414515+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNI3 was added\ngene: TNNI3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TNNI3 was set to Unknown","entity_name":"TNNI3","entity_type":"gene"},{"created":"2020-11-09T16:41:58.373234+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM43 was added\ngene: TMEM43 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TMEM43 was set to Unknown","entity_name":"TMEM43","entity_type":"gene"},{"created":"2020-11-09T16:41:58.334265+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN5A was added\ngene: SCN5A was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SCN5A was set to Unknown","entity_name":"SCN5A","entity_type":"gene"},{"created":"2020-11-09T16:41:58.295873+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RYR2 was added\ngene: RYR2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RYR2 was set to Unknown","entity_name":"RYR2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.257996+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRKAG2 was added\ngene: PRKAG2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PRKAG2 was set to Unknown","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.220281+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PKP2 was added\ngene: PKP2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PKP2 was set to Unknown","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.182043+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LMNA was added\ngene: LMNA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: LMNA was set to Unknown","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-11-09T16:41:58.143969+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYH7 was added\ngene: MYH7 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYH7 was set to Unknown","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-11-09T16:41:58.105190+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYL3 was added\ngene: MYL3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYL3 was set to Unknown","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-11-09T16:41:58.067204+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYL2 was added\ngene: MYL2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYL2 was set to Unknown","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-11-09T16:41:58.029450+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYBPC3 was added\ngene: MYBPC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYBPC3 was set to Unknown","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-11-09T16:41:57.991909+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNH2 was added\ngene: KCNH2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: KCNH2 was set to Unknown","entity_name":"KCNH2","entity_type":"gene"},{"created":"2020-11-09T16:41:57.955064+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNQ1 was added\ngene: KCNQ1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: KCNQ1 was set to Unknown","entity_name":"KCNQ1","entity_type":"gene"},{"created":"2020-11-09T16:41:57.917076+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GLA was added\ngene: GLA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GLA was set to Unknown","entity_name":"GLA","entity_type":"gene"},{"created":"2020-11-09T16:41:57.880011+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DSP was added\ngene: DSP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSP was set to Unknown","entity_name":"DSP","entity_type":"gene"},{"created":"2020-11-09T16:41:57.839053+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DSG2 was added\ngene: DSG2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSG2 was set to Unknown","entity_name":"DSG2","entity_type":"gene"},{"created":"2020-11-09T16:41:57.775067+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DSC2 was added\ngene: DSC2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSC2 was set to Unknown","entity_name":"DSC2","entity_type":"gene"},{"created":"2020-11-09T16:41:57.731750+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ACTC1 was added\ngene: ACTC1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ACTC1 was set to Unknown","entity_name":"ACTC1","entity_type":"gene"},{"created":"2020-11-09T16:41:57.693647+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WT1 was added\ngene: WT1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: WT1 was set to Unknown","entity_name":"WT1","entity_type":"gene"},{"created":"2020-11-09T16:41:57.651904+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STK11 was added\ngene: STK11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: STK11 was set to Unknown","entity_name":"STK11","entity_type":"gene"},{"created":"2020-11-09T16:41:57.610270+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RB1 was added\ngene: RB1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RB1 was set to Unknown","entity_name":"RB1","entity_type":"gene"},{"created":"2020-11-09T16:41:57.568244+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BRCA2 was added\ngene: BRCA2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRCA2 was set to Unknown","entity_name":"BRCA2","entity_type":"gene"},{"created":"2020-11-09T16:41:57.530339+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BRCA1 was added\ngene: BRCA1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRCA1 was set to Unknown","entity_name":"BRCA1","entity_type":"gene"},{"created":"2020-11-09T16:41:57.492574+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP7B was added\ngene: ATP7B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ATP7B was set to Unknown","entity_name":"ATP7B","entity_type":"gene"},{"created":"2020-11-09T16:41:57.447517+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GBA was added\ngene: GBA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GBA was set to Unknown","entity_name":"GBA","entity_type":"gene"},{"created":"2020-11-09T16:41:57.403921+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SNCB was added\ngene: SNCB was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SNCB was set to Unknown","entity_name":"SNCB","entity_type":"gene"},{"created":"2020-11-09T16:41:57.364385+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SNCA was added\ngene: SNCA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SNCA was set to Unknown","entity_name":"SNCA","entity_type":"gene"},{"created":"2020-11-09T16:41:57.323091+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TARDBP was added\ngene: TARDBP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TARDBP was set to Unknown","entity_name":"TARDBP","entity_type":"gene"},{"created":"2020-11-09T16:41:57.284297+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CHMP2B was added\ngene: CHMP2B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CHMP2B was set to Unknown","entity_name":"CHMP2B","entity_type":"gene"},{"created":"2020-11-09T16:41:57.245744+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: C9orf72 was added\ngene: C9orf72 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: C9orf72 was set to Unknown","entity_name":"C9orf72","entity_type":"gene"},{"created":"2020-11-09T16:41:57.205149+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GRN was added\ngene: GRN was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GRN was set to Unknown","entity_name":"GRN","entity_type":"gene"},{"created":"2020-11-09T16:41:57.164719+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MAPT was added\ngene: MAPT was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MAPT was set to Unknown","entity_name":"MAPT","entity_type":"gene"},{"created":"2020-11-09T16:41:57.126955+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ITM2B was added\ngene: ITM2B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ITM2B was set to Unknown","entity_name":"ITM2B","entity_type":"gene"},{"created":"2020-11-09T16:41:57.085700+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CST3 was added\ngene: CST3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CST3 was set to Unknown","entity_name":"CST3","entity_type":"gene"},{"created":"2020-11-09T16:41:57.047319+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NOTCH3 was added\ngene: NOTCH3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: NOTCH3 was set to Unknown","entity_name":"NOTCH3","entity_type":"gene"},{"created":"2020-11-09T16:41:57.011065+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SQSTM1 was added\ngene: SQSTM1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SQSTM1 was set to Unknown","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2020-11-09T16:41:56.973503+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VCP was added\ngene: VCP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: VCP was set to Unknown","entity_name":"VCP","entity_type":"gene"},{"created":"2020-11-09T16:41:56.936051+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TYROBP was added\ngene: TYROBP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TYROBP was set to Unknown","entity_name":"TYROBP","entity_type":"gene"},{"created":"2020-11-09T16:41:56.899455+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TREM2 was added\ngene: TREM2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TREM2 was set to Unknown","entity_name":"TREM2","entity_type":"gene"},{"created":"2020-11-09T16:41:56.853031+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PSEN2 was added\ngene: PSEN2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PSEN2 was set to Unknown","entity_name":"PSEN2","entity_type":"gene"},{"created":"2020-11-09T16:41:56.812414+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PSEN1 was added\ngene: PSEN1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PSEN1 was set to Unknown","entity_name":"PSEN1","entity_type":"gene"},{"created":"2020-11-09T16:41:56.770279+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: APP was added\ngene: APP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: APP was set to Unknown","entity_name":"APP","entity_type":"gene"},{"created":"2020-11-09T16:41:56.743645+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Incidentalome_NSW","entity_name":null,"entity_type":null},{"created":"2020-11-07T15:31:28.703046+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATAD3A as ready","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:31:28.694147+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad3a has been classified as Green List (High Evidence).","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:31:26.373719+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATAD3A were changed from 618810 to Harel-Yoon syndrome, MIM# 617183; Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal (PHRINL SYNDROME), MIM# 618810; perinatal cardiomyopathy; cataracts; corneal clouding","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:31:14.710526+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATAD3A were set to PMID: 32004445","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:30:56.344827+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ATAD3A.","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:30:50.583984+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATAD3A as Green List (high evidence)","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:30:50.574453+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad3a has been classified as Green List (High Evidence).","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:29:48.307598+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.38","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 32004445, PMID: 27640307, PMID: 28549128, also Frazier et al, Med (in press); Phenotypes: Harel-Yoon syndrome, MIM# 617183, Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal (PHRINL SYNDROME), MIM# 618810, perinatal cardiomyopathy, cataracts, corneal clouding; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:29:37.432027+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5338","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACAD9 as ready","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:29:37.423362+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5338","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acad9 has been classified as Green List (High Evidence).","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:29:30.229167+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5338","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACAD9 were changed from  to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:29:12.666132+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5337","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACAD9 were set to ","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:28:54.724246+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5336","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:28:36.712718+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5335","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:27:21.964993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5335","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNP were changed from Hypomyelinating leukodystrophy to Leukodystrophy, hypomyelinating, 20, MIM# 619071","entity_name":"CNP","entity_type":"gene"},{"created":"2020-11-07T15:26:59.865157+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5334","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CNP: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukodystrophy, hypomyelinating, 20, MIM# 619071; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNP","entity_type":"gene"},{"created":"2020-11-07T15:26:38.773455+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNP were changed from Hypomyelinating leukodystrophy to Leukodystrophy, hypomyelinating, 20, MIM# 619071","entity_name":"CNP","entity_type":"gene"},{"created":"2020-11-07T15:26:20.922182+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CNP: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukodystrophy, hypomyelinating, 20, MIM# 619071; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNP","entity_type":"gene"},{"created":"2020-11-07T15:14:56.205754+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.38","user_name":"John Christodoulou","item_type":"entity","text":"gene: ATAD3A was added\ngene: ATAD3A was added to Cardiomyopathy_Paediatric. Sources: Literature,Expert Review\nMode of inheritance for gene: ATAD3A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ATAD3A were set to PMID: 32004445\nPhenotypes for gene: ATAD3A were set to 618810\nPenetrance for gene: ATAD3A were set to Complete","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-11-07T15:00:02.255159+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.553","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACAD9 as ready","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T15:00:02.235095+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.553","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acad9 has been classified as Green List (High Evidence).","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:59:59.457122+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.553","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACAD9 were changed from  to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:59:30.353856+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.552","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACAD9 were set to ","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:59:01.420248+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.551","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:58:32.953758+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.550","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:27:16.419688+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACAD9 as ready","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:27:16.409818+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acad9 has been classified as Green List (High Evidence).","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:26:56.845591+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACAD9 were changed from  to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:26:29.807550+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3180","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACAD9 were set to ","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:26:02.217661+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3179","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-07T14:25:27.945085+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3178","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-11-06T16:11:42.422916+11:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.47","user_name":"Sarah Righetti","item_type":"entity","text":"reviewed gene: NEXMIF: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 98, MIM #300912; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"NEXMIF","entity_type":"gene"},{"created":"2020-11-06T16:06:06.433198+11:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.47","user_name":"Sarah Righetti","item_type":"entity","text":"reviewed gene: CLCN4: Rating: GREEN; Mode of pathogenicity: None; Publications: 27550844; Phenotypes: Raynaud-Claes syndrome, MIM #300114; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"CLCN4","entity_type":"gene"},{"created":"2020-11-06T16:02:57.558091+11:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.47","user_name":"Sarah Righetti","item_type":"entity","text":"Deleted their comment","entity_name":"NYX","entity_type":"gene"},{"created":"2020-11-06T16:02:53.668950+11:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.47","user_name":"Sarah Righetti","item_type":"entity","text":"edited their review of gene: NYX: Added comment: Clinical summary: Function of rods disrupted - difficulty seeing in low light. Other vision problems including reduced acuity (20/30 to 20/200) which is considered mild-moderate visual impairment or reduced-low vision. 20/40 is Australian legal driving limit. Myopia - can range from low to high. May have nystagmus/strabismus. Color vision not affected. Non-progressive, present at birth.\r\n\r\nSevere end of phenoypic spectrum meets MM criteria for inclusion - GREEN; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NYX","entity_type":"gene"},{"created":"2020-11-06T16:02:32.042730+11:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.47","user_name":"Sarah Righetti","item_type":"entity","text":"reviewed gene: NYX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1A, X-linked, MIM #310500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NYX","entity_type":"gene"}]}