{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2190","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2188","results":[{"created":"2019-11-17T16:46:00.755786+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC6A5 was added\ngene: SLC6A5 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC6A5 was set to Unknown","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2019-11-17T16:46:00.684799+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC2A1 was added\ngene: SLC2A1 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC2A1 was set to Unknown","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2019-11-17T16:46:00.613673+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC1A3 was added\ngene: SLC1A3 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC1A3 was set to Unknown","entity_name":"SLC1A3","entity_type":"gene"},{"created":"2019-11-17T16:46:00.543631+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN8A was added\ngene: SCN8A was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN8A was set to Unknown","entity_name":"SCN8A","entity_type":"gene"},{"created":"2019-11-17T16:46:00.474387+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN4A was added\ngene: SCN4A was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN4A was set to Unknown","entity_name":"SCN4A","entity_type":"gene"},{"created":"2019-11-17T16:46:00.403887+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN1A was added\ngene: SCN1A was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN1A was set to Unknown","entity_name":"SCN1A","entity_type":"gene"},{"created":"2019-11-17T16:46:00.333707+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRRT2 was added\ngene: PRRT2 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PRRT2 was set to Unknown","entity_name":"PRRT2","entity_type":"gene"},{"created":"2019-11-17T16:46:00.263573+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PNKD was added\ngene: PNKD was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PNKD was set to Unknown","entity_name":"PNKD","entity_type":"gene"},{"created":"2019-11-17T16:46:00.194739+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNQ3 was added\ngene: KCNQ3 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNQ3 was set to Unknown","entity_name":"KCNQ3","entity_type":"gene"},{"created":"2019-11-17T16:46:00.126071+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNQ2 was added\ngene: KCNQ2 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNQ2 was set to Unknown","entity_name":"KCNQ2","entity_type":"gene"},{"created":"2019-11-17T16:46:00.002825+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNMA1 was added\ngene: KCNMA1 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNMA1 was set to Unknown","entity_name":"KCNMA1","entity_type":"gene"},{"created":"2019-11-17T16:45:59.932026+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNJ2 was added\ngene: KCNJ2 was added to Channelopathy_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":"2019-11-17T16:45:59.862631+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNA1 was added\ngene: KCNA1 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNA1 was set to Unknown","entity_name":"KCNA1","entity_type":"gene"},{"created":"2019-11-17T16:45:59.793778+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GLRB was added\ngene: GLRB was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GLRB was set to Unknown","entity_name":"GLRB","entity_type":"gene"},{"created":"2019-11-17T16:45:59.726134+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GLRA1 was added\ngene: GLRA1 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GLRA1 was set to Unknown","entity_name":"GLRA1","entity_type":"gene"},{"created":"2019-11-17T16:45:59.658411+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CACNB4 was added\ngene: CACNB4 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNB4 was set to Unknown","entity_name":"CACNB4","entity_type":"gene"},{"created":"2019-11-17T16:45:59.591160+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CACNA1S was added\ngene: CACNA1S was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNA1S was set to Unknown","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2019-11-17T16:45:59.524775+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CACNA1A was added\ngene: CACNA1A was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNA1A was set to Unknown","entity_name":"CACNA1A","entity_type":"gene"},{"created":"2019-11-17T16:45:59.456122+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP7B was added\ngene: ATP7B was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATP7B was set to Unknown","entity_name":"ATP7B","entity_type":"gene"},{"created":"2019-11-17T16:45:59.390182+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP1A3 was added\ngene: ATP1A3 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATP1A3 was set to Unknown","entity_name":"ATP1A3","entity_type":"gene"},{"created":"2019-11-17T16:45:59.323550+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATP1A2 was added\ngene: ATP1A2 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATP1A2 was set to Unknown","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2019-11-17T16:45:59.255620+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADCY5 was added\ngene: ADCY5 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ADCY5 was set to Unknown","entity_name":"ADCY5","entity_type":"gene"},{"created":"2019-11-17T16:45:59.213820+11:00","panel_name":"Channelopathy_VCGS","panel_id":74,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Channelopathy_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:45:42.393615+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZC4H2 was added\ngene: ZC4H2 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZC4H2 was set to Unknown","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2019-11-17T16:45:42.322417+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS13D was added\ngene: VPS13D was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VPS13D was set to Unknown","entity_name":"VPS13D","entity_type":"gene"},{"created":"2019-11-17T16:45:42.254861+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA1A was added\ngene: TUBA1A was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBA1A was set to Unknown","entity_name":"TUBA1A","entity_type":"gene"},{"created":"2019-11-17T16:45:42.186767+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TENM1 was added\ngene: TENM1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TENM1 was set to Unknown","entity_name":"TENM1","entity_type":"gene"},{"created":"2019-11-17T16:45:42.118158+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN8A was added\ngene: SCN8A was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN8A was set to Unknown","entity_name":"SCN8A","entity_type":"gene"},{"created":"2019-11-17T16:45:41.989094+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PCYT2 was added\ngene: PCYT2 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PCYT2 was set to Unknown","entity_name":"PCYT2","entity_type":"gene"},{"created":"2019-11-17T16:45:41.920515+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PAK3 was added\ngene: PAK3 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PAK3 was set to Unknown","entity_name":"PAK3","entity_type":"gene"},{"created":"2019-11-17T16:45:41.849620+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NKX2-1 was added\ngene: NKX2-1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NKX2-1 was set to Unknown","entity_name":"NKX2-1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.780058+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: L1CAM was added\ngene: L1CAM was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: L1CAM was set to Unknown","entity_name":"L1CAM","entity_type":"gene"},{"created":"2019-11-17T16:45:41.712769+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KDM5C was added\ngene: KDM5C was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KDM5C was set to Unknown","entity_name":"KDM5C","entity_type":"gene"},{"created":"2019-11-17T16:45:41.646242+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KANK1 was added\ngene: KANK1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KANK1 was set to Unknown","entity_name":"KANK1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.578452+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GAD1 was added\ngene: GAD1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GAD1 was set to Unknown","entity_name":"GAD1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.512849+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP4S1 was added\ngene: AP4S1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP4S1 was set to Unknown","entity_name":"AP4S1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.446733+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP4M1 was added\ngene: AP4M1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP4M1 was set to Unknown","entity_name":"AP4M1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.379440+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP4E1 was added\ngene: AP4E1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP4E1 was set to Unknown","entity_name":"AP4E1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.311427+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP4B1 was added\ngene: AP4B1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP4B1 was set to Unknown","entity_name":"AP4B1","entity_type":"gene"},{"created":"2019-11-17T16:45:41.269512+11:00","panel_name":"Cerebral Palsy_VCGS","panel_id":73,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Cerebral Palsy_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:45:25.685743+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR91 was added\ngene: WDR91 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR91 was set to Unknown","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-11-17T16:45:25.612226+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR37 was added\ngene: WDR37 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR37 was set to Unknown","entity_name":"WDR37","entity_type":"gene"},{"created":"2019-11-17T16:45:25.536762+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VRK1 was added\ngene: VRK1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VRK1 was set to Unknown","entity_name":"VRK1","entity_type":"gene"},{"created":"2019-11-17T16:45:25.463498+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS53 was added\ngene: VPS53 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VPS53 was set to Unknown","entity_name":"VPS53","entity_type":"gene"},{"created":"2019-11-17T16:45:25.390367+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VLDLR was added\ngene: VLDLR was added to Cerebellar and Pontocerebellar hypoplasia_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":"2019-11-17T16:45:25.315800+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UFM1 was added\ngene: UFM1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: UFM1 was set to Unknown","entity_name":"UFM1","entity_type":"gene"},{"created":"2019-11-17T16:45:25.240856+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB3 was added\ngene: TUBB3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBB3 was set to Unknown","entity_name":"TUBB3","entity_type":"gene"},{"created":"2019-11-17T16:45:25.167814+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB2B was added\ngene: TUBB2B was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBB2B was set to Unknown","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2019-11-17T16:45:24.991380+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA8 was added\ngene: TUBA8 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBA8 was set to Unknown","entity_name":"TUBA8","entity_type":"gene"},{"created":"2019-11-17T16:45:24.920516+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA1A was added\ngene: TUBA1A was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBA1A was set to Unknown","entity_name":"TUBA1A","entity_type":"gene"},{"created":"2019-11-17T16:45:24.848262+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSEN54 was added\ngene: TSEN54 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSEN54 was set to Unknown","entity_name":"TSEN54","entity_type":"gene"},{"created":"2019-11-17T16:45:24.774092+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSEN34 was added\ngene: TSEN34 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSEN34 was set to Unknown","entity_name":"TSEN34","entity_type":"gene"},{"created":"2019-11-17T16:45:24.700336+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSEN2 was added\ngene: TSEN2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSEN2 was set to Unknown","entity_name":"TSEN2","entity_type":"gene"},{"created":"2019-11-17T16:45:24.629622+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSEN15 was added\ngene: TSEN15 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSEN15 was set to Unknown","entity_name":"TSEN15","entity_type":"gene"},{"created":"2019-11-17T16:45:24.556938+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRAPPC6B was added\ngene: TRAPPC6B was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TRAPPC6B was set to Unknown","entity_name":"TRAPPC6B","entity_type":"gene"},{"created":"2019-11-17T16:45:24.483008+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TOE1 was added\ngene: TOE1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TOE1 was set to Unknown","entity_name":"TOE1","entity_type":"gene"},{"created":"2019-11-17T16:45:24.411007+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBCK was added\ngene: TBCK was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TBCK was set to Unknown","entity_name":"TBCK","entity_type":"gene"},{"created":"2019-11-17T16:45:24.340251+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBC1D23 was added\ngene: TBC1D23 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TBC1D23 was set to Unknown","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2019-11-17T16:45:24.270031+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPTBN2 was added\ngene: SPTBN2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPTBN2 was set to Unknown","entity_name":"SPTBN2","entity_type":"gene"},{"created":"2019-11-17T16:45:24.200130+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC25A46 was added\ngene: SLC25A46 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC25A46 was set to Unknown","entity_name":"SLC25A46","entity_type":"gene"},{"created":"2019-11-17T16:45:24.129664+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SETD2 was added\ngene: SETD2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SETD2 was set to Unknown","entity_name":"SETD2","entity_type":"gene"},{"created":"2019-11-17T16:45:23.997056+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SEPSECS was added\ngene: SEPSECS was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SEPSECS was set to Unknown","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2019-11-17T16:45:23.926518+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RELN was added\ngene: RELN was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RELN was set to Unknown","entity_name":"RELN","entity_type":"gene"},{"created":"2019-11-17T16:45:23.855996+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RARS2 was added\ngene: RARS2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RARS2 was set to Unknown","entity_name":"RARS2","entity_type":"gene"},{"created":"2019-11-17T16:45:23.784303+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RAB11B was added\ngene: RAB11B was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RAB11B was set to Unknown","entity_name":"RAB11B","entity_type":"gene"},{"created":"2019-11-17T16:45:23.713236+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PUS3 was added\ngene: PUS3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PUS3 was set to Unknown","entity_name":"PUS3","entity_type":"gene"},{"created":"2019-11-17T16:45:23.642614+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PPP1CB was added\ngene: PPP1CB was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PPP1CB was set to Unknown","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2019-11-17T16:45:23.572921+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PCLO was added\ngene: PCLO was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PCLO was set to Unknown","entity_name":"PCLO","entity_type":"gene"},{"created":"2019-11-17T16:45:23.503207+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: OPHN1 was added\ngene: OPHN1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OPHN1 was set to Unknown","entity_name":"OPHN1","entity_type":"gene"},{"created":"2019-11-17T16:45:23.433855+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KIAA1109 was added\ngene: KIAA1109 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIAA1109 was set to Unknown","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2019-11-17T16:45:23.364245+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KCNC3 was added\ngene: KCNC3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNC3 was set to Unknown","entity_name":"KCNC3","entity_type":"gene"},{"created":"2019-11-17T16:45:23.294638+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KAT5 was added\ngene: KAT5 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KAT5 was set to Unknown","entity_name":"KAT5","entity_type":"gene"},{"created":"2019-11-17T16:45:23.225633+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ITPR1 was added\ngene: ITPR1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ITPR1 was set to Unknown","entity_name":"ITPR1","entity_type":"gene"},{"created":"2019-11-17T16:45:23.156327+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: INTS8 was added\ngene: INTS8 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: INTS8 was set to Unknown","entity_name":"INTS8","entity_type":"gene"},{"created":"2019-11-17T16:45:23.087162+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GPAA1 was added\ngene: GPAA1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GPAA1 was set to Unknown","entity_name":"GPAA1","entity_type":"gene"},{"created":"2019-11-17T16:45:23.001072+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FZD3 was added\ngene: FZD3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FZD3 was set to Unknown","entity_name":"FZD3","entity_type":"gene"},{"created":"2019-11-17T16:45:22.932110+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FOXP1 was added\ngene: FOXP1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FOXP1 was set to Unknown","entity_name":"FOXP1","entity_type":"gene"},{"created":"2019-11-17T16:45:22.862385+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EXOSC9 was added\ngene: EXOSC9 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EXOSC9 was set to Unknown","entity_name":"EXOSC9","entity_type":"gene"},{"created":"2019-11-17T16:45:22.793807+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EXOSC8 was added\ngene: EXOSC8 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EXOSC8 was set to Unknown","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2019-11-17T16:45:22.724413+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EXOSC5 was added\ngene: EXOSC5 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EXOSC5 was set to Unknown","entity_name":"EXOSC5","entity_type":"gene"},{"created":"2019-11-17T16:45:22.656396+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EXOSC3 was added\ngene: EXOSC3 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EXOSC3 was set to Unknown","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2019-11-17T16:45:22.588494+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DDX3X was added\ngene: DDX3X was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DDX3X was set to Unknown","entity_name":"DDX3X","entity_type":"gene"},{"created":"2019-11-17T16:45:22.519251+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLP1 was added\ngene: CLP1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CLP1 was set to Unknown","entity_name":"CLP1","entity_type":"gene"},{"created":"2019-11-17T16:45:22.450705+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CHMP1A was added\ngene: CHMP1A was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CHMP1A was set to Unknown","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2019-11-17T16:45:22.382178+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CEP55 was added\ngene: CEP55 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP55 was set to Unknown","entity_name":"CEP55","entity_type":"gene"},{"created":"2019-11-17T16:45:22.314889+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CASK was added\ngene: CASK was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CASK was set to Unknown","entity_name":"CASK","entity_type":"gene"},{"created":"2019-11-17T16:45:22.247602+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BRF1 was added\ngene: BRF1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BRF1 was set to Unknown","entity_name":"BRF1","entity_type":"gene"},{"created":"2019-11-17T16:45:22.180193+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BCL11A was added\ngene: BCL11A was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BCL11A was set to Unknown","entity_name":"BCL11A","entity_type":"gene"},{"created":"2019-11-17T16:45:22.113692+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AUTS2 was added\ngene: AUTS2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AUTS2 was set to Unknown","entity_name":"AUTS2","entity_type":"gene"},{"created":"2019-11-17T16:45:22.045936+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AMPD2 was added\ngene: AMPD2 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AMPD2 was set to Unknown","entity_name":"AMPD2","entity_type":"gene"},{"created":"2019-11-17T16:45:22.002265+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Cerebellar and Pontocerebellar hypoplasia_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:45:02.172483+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RET was added\ngene: RET was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RET was set to Unknown","entity_name":"RET","entity_type":"gene"},{"created":"2019-11-17T16:45:02.089417+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PHOX2B was added\ngene: PHOX2B was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PHOX2B was set to Unknown","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2019-11-17T16:45:01.999826+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GDNF was added\ngene: GDNF was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GDNF was set to Unknown","entity_name":"GDNF","entity_type":"gene"},{"created":"2019-11-17T16:45:01.928683+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EDN3 was added\ngene: EDN3 was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: EDN3 was set to Unknown","entity_name":"EDN3","entity_type":"gene"},{"created":"2019-11-17T16:45:01.858197+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BDNF was added\ngene: BDNF was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BDNF was set to Unknown","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-11-17T16:45:01.783546+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ASCL1 was added\ngene: ASCL1 was added to Central Hypoventilation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ASCL1 was set to Unknown","entity_name":"ASCL1","entity_type":"gene"},{"created":"2019-11-17T16:45:01.735241+11:00","panel_name":"Central Hypoventilation_VCGS","panel_id":71,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Central Hypoventilation_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-17T16:44:25.990869+11:00","panel_name":"Congenital diaphragmatic hernia, CDH_VCGS","panel_id":69,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WT1 was added\ngene: WT1 was added to Congenital diaphragmatic hernia, CDH_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":"2019-11-17T16:44:25.920614+11:00","panel_name":"Congenital diaphragmatic hernia, CDH_VCGS","panel_id":69,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STRA6 was added\ngene: STRA6 was added to Congenital diaphragmatic hernia, CDH_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STRA6 was set to Unknown","entity_name":"STRA6","entity_type":"gene"}]}