HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220842,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1966",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}