{"count":220842,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1966","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1964","results":[{"created":"2020-01-24T15:59:15.749225+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.345","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LYST was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LYST","entity_type":"gene"},{"created":"2020-01-24T15:58:41.915838+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LYST as Amber List (moderate evidence)","entity_name":"LYST","entity_type":"gene"},{"created":"2020-01-24T15:58:41.901986+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Amber List (Moderate Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2020-01-24T15:58:00.998777+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LYST: Rating: AMBER; Mode of pathogenicity: None; Publications: 10450360; Phenotypes: Chediak-Higashi syndrome, MIM#214500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LYST","entity_type":"gene"},{"created":"2020-01-24T15:57:06.751064+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LNPK were changed from Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum, MIM# 618090 to Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum, MIM# 618090","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:56:46.123357+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LNPK as ready","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:56:45.888989+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lnpk has been classified as Amber List (Moderate Evidence).","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:56:34.868250+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LNPK were set to 30032983","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:56:04.230596+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LNPK were changed from  to Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum, MIM# 618090","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:55:33.829667+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LNPK were set to ","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:55:03.493647+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LNPK was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:52:12.234441+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: SOX18 as Red List (low evidence)","entity_name":"SOX18","entity_type":"gene"},{"created":"2020-01-24T15:52:12.231386+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On the lymphoedema panel instead","entity_name":"SOX18","entity_type":"gene"},{"created":"2020-01-24T15:52:12.202579+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sox18 has been classified as Red List (Low Evidence).","entity_name":"SOX18","entity_type":"gene"},{"created":"2020-01-24T15:49:04.479530+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.341","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LNPK as Amber List (moderate evidence)","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:49:04.471293+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.341","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lnpk has been classified as Amber List (Moderate Evidence).","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:47:48.310324+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.340","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LNPK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:47:03.621572+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.339","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LNPK: Rating: GREEN; Mode of pathogenicity: None; Publications: 30032983; Phenotypes: Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum, MIM# 618090; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LNPK","entity_type":"gene"},{"created":"2020-01-24T15:45:03.049812+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: BMPR1B as Red List (low evidence)","entity_name":"BMPR1B","entity_type":"gene"},{"created":"2020-01-24T15:45:03.046277+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"BMPR1B","entity_type":"gene"},{"created":"2020-01-24T15:45:03.012837+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: bmpr1b has been classified as Red List (Low Evidence).","entity_name":"BMPR1B","entity_type":"gene"},{"created":"2020-01-24T15:44:17.467871+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: TBX4 as Red List (low evidence)","entity_name":"TBX4","entity_type":"gene"},{"created":"2020-01-24T15:44:17.464676+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"TBX4","entity_type":"gene"},{"created":"2020-01-24T15:44:17.436132+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: tbx4 has been classified as Red List (Low Evidence).","entity_name":"TBX4","entity_type":"gene"},{"created":"2020-01-24T15:42:09.868305+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1672","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:LNP1 from the panel","entity_name":null,"entity_type":null},{"created":"2020-01-24T15:41:13.582132+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.339","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:LNP1 from the panel","entity_name":null,"entity_type":null},{"created":"2020-01-24T15:40:50.751777+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.338","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPT2 as ready","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:40:50.742894+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.338","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt2 has been classified as Green List (High Evidence).","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:39:57.910706+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.948","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:LNP1 from the panel","entity_name":null,"entity_type":null},{"created":"2020-01-24T15:38:46.110222+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: SOX17 as Red List (low evidence)","entity_name":"SOX17","entity_type":"gene"},{"created":"2020-01-24T15:38:46.106922+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"SOX17","entity_type":"gene"},{"created":"2020-01-24T15:38:46.078944+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sox17 has been classified as Red List (Low Evidence).","entity_name":"SOX17","entity_type":"gene"},{"created":"2020-01-24T15:37:17.336423+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: SMAD9 as Red List (low evidence)","entity_name":"SMAD9","entity_type":"gene"},{"created":"2020-01-24T15:37:17.333077+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to the pulmonary arterial hypertension panel","entity_name":"SMAD9","entity_type":"gene"},{"created":"2020-01-24T15:37:17.304185+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: smad9 has been classified as Red List (Low Evidence).","entity_name":"SMAD9","entity_type":"gene"},{"created":"2020-01-24T15:36:57.338973+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.338","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPT2 were changed from Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668 to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:36:20.368794+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPT2 were changed from  to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:36:13.146809+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARGE1 as ready","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:36:13.131129+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: large1 has been classified as Amber List (Moderate Evidence).","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:35:55.176685+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPT2 were set to ","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:35:18.681709+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.336","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARGE1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, MIM#613154; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6, MIM#608840","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:34:47.442341+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.336","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LIPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:34:07.482532+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.335","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LIPT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 28757203; Phenotypes: Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPT2","entity_type":"gene"},{"created":"2020-01-24T15:32:46.173555+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.335","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARGE1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:30:24.324933+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LARGE1 as Amber List (moderate evidence)","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:30:24.316930+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: large1 has been classified as Amber List (Moderate Evidence).","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:29:46.415460+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.333","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LARGE1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, MIM#613154, Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6, MIM#608840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-01-24T15:28:44.321868+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.333","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KPTN as ready","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:28:44.314655+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.333","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kptn has been classified as Amber List (Moderate Evidence).","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:25:25.395377+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.333","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KPTN were changed from  to Mental retardation, autosomal recessive 4, MIM#1615637","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:24:51.698168+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.332","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KPTN were set to ","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:24:17.363766+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.331","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KPTN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:24:09.353318+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: PTPN14 as ready","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:24:09.342844+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: ptpn14 has been classified as Red List (Low Evidence).","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:24:01.131131+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PTPN14 as Red List (low evidence)","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:24:01.125889+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: No evidence for vascular malformations. The gene has been added to the lymphoedema panel.","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:24:01.101131+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: ptpn14 has been classified as Red List (Low Evidence).","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:23:39.980343+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.330","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KPTN as Amber List (moderate evidence)","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:23:39.972701+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.330","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kptn has been classified as Amber List (Moderate Evidence).","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:23:00.546601+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.329","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KPTN: Rating: AMBER; Mode of pathogenicity: None; Publications: 25847626, 24239382; Phenotypes: Mental retardation, autosomal recessive 4, MIM#1615637; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KPTN","entity_type":"gene"},{"created":"2020-01-24T15:22:52.223175+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: PTPN14: Rating: RED; Mode of pathogenicity: None; Publications: 22233626, 29932521; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:20:00.908083+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Deleted their review","entity_name":"PTPN14","entity_type":"gene"},{"created":"2020-01-24T15:11:51.352978+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PIEZO1 as Red List (low evidence)","entity_name":"PIEZO1","entity_type":"gene"},{"created":"2020-01-24T15:11:51.349775+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On the lymphoedema panel instead","entity_name":"PIEZO1","entity_type":"gene"},{"created":"2020-01-24T15:11:51.322776+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: piezo1 has been classified as Red List (Low Evidence).","entity_name":"PIEZO1","entity_type":"gene"},{"created":"2020-01-24T15:10:44.318158+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KIF11 as Red List (low evidence)","entity_name":"KIF11","entity_type":"gene"},{"created":"2020-01-24T15:10:44.313867+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On the lymphoedema panel instead","entity_name":"KIF11","entity_type":"gene"},{"created":"2020-01-24T15:10:44.286928+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kif11 has been classified as Red List (Low Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2020-01-24T15:10:04.303365+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KCNK3 as Red List (low evidence)","entity_name":"KCNK3","entity_type":"gene"},{"created":"2020-01-24T15:10:04.300191+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to the Pulmonary arterial hypertension panel","entity_name":"KCNK3","entity_type":"gene"},{"created":"2020-01-24T15:10:04.269771+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kcnk3 has been classified as Red List (Low Evidence).","entity_name":"KCNK3","entity_type":"gene"},{"created":"2020-01-24T15:00:10.850164+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: GJC2 as Red List (low evidence)","entity_name":"GJC2","entity_type":"gene"},{"created":"2020-01-24T15:00:10.846888+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"GJC2","entity_type":"gene"},{"created":"2020-01-24T15:00:10.815782+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: gjc2 has been classified as Red List (Low Evidence).","entity_name":"GJC2","entity_type":"gene"},{"created":"2020-01-24T14:59:15.417861+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: GATA2 as Red List (low evidence)","entity_name":"GATA2","entity_type":"gene"},{"created":"2020-01-24T14:59:15.414587+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"GATA2","entity_type":"gene"},{"created":"2020-01-24T14:59:15.383206+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: gata2 has been classified as Red List (Low Evidence).","entity_name":"GATA2","entity_type":"gene"},{"created":"2020-01-24T14:58:33.040303+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.49","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: FOXC2 as Red List (low evidence)","entity_name":"FOXC2","entity_type":"gene"},{"created":"2020-01-24T14:58:33.037114+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.49","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"FOXC2","entity_type":"gene"},{"created":"2020-01-24T14:58:33.007159+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.49","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: foxc2 has been classified as Red List (Low Evidence).","entity_name":"FOXC2","entity_type":"gene"},{"created":"2020-01-24T14:57:52.264739+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.48","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: FLT4 as Red List (low evidence)","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-01-24T14:57:52.261495+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.48","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-01-24T14:57:52.234726+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.48","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: flt4 has been classified as Red List (Low Evidence).","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-01-24T14:57:19.671581+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.47","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: FAT4 as Red List (low evidence)","entity_name":"FAT4","entity_type":"gene"},{"created":"2020-01-24T14:57:19.667831+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.47","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"FAT4","entity_type":"gene"},{"created":"2020-01-24T14:57:19.636950+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.47","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: fat4 has been classified as Red List (Low Evidence).","entity_name":"FAT4","entity_type":"gene"},{"created":"2020-01-24T14:56:25.863686+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.46","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: EIF2AK4 as Red List (low evidence)","entity_name":"EIF2AK4","entity_type":"gene"},{"created":"2020-01-24T14:56:25.860567+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.46","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"EIF2AK4","entity_type":"gene"},{"created":"2020-01-24T14:56:25.831916+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.46","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: eif2ak4 has been classified as Red List (Low Evidence).","entity_name":"EIF2AK4","entity_type":"gene"},{"created":"2020-01-24T14:55:38.562706+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.45","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: CCBE1 as Red List (low evidence)","entity_name":"CCBE1","entity_type":"gene"},{"created":"2020-01-24T14:55:38.558625+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.45","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: On lymphoedema panel instead","entity_name":"CCBE1","entity_type":"gene"},{"created":"2020-01-24T14:55:38.529385+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.45","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: ccbe1 has been classified as Red List (Low Evidence).","entity_name":"CCBE1","entity_type":"gene"},{"created":"2020-01-24T14:54:38.225987+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.44","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: CAV1 as Red List (low evidence)","entity_name":"CAV1","entity_type":"gene"},{"created":"2020-01-24T14:54:38.222314+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.44","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"CAV1","entity_type":"gene"},{"created":"2020-01-24T14:54:38.194311+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.44","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: cav1 has been classified as Red List (Low Evidence).","entity_name":"CAV1","entity_type":"gene"},{"created":"2020-01-24T14:54:13.501208+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.43","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: BMPR2 as Red List (low evidence)","entity_name":"BMPR2","entity_type":"gene"},{"created":"2020-01-24T14:54:13.498065+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.43","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"BMPR2","entity_type":"gene"},{"created":"2020-01-24T14:54:13.468308+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.43","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: bmpr2 has been classified as Red List (Low Evidence).","entity_name":"BMPR2","entity_type":"gene"},{"created":"2020-01-24T14:53:07.345414+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.42","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: ATP13A3 as Red List (low evidence)","entity_name":"ATP13A3","entity_type":"gene"},{"created":"2020-01-24T14:53:07.342159+11:00","panel_name":"Inherited Vascular Malformations","panel_id":300,"panel_version":"0.42","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Moved to pulmonary arterial hypertension panel","entity_name":"ATP13A3","entity_type":"gene"}]}