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{
"count": 220497,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1550",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1548",
"results": [
{
"created": "2020-10-07T21:50:46.022050+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FKTN as ready",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:50:46.006759+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fktn has been classified as Red List (Low Evidence).",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:50:07.575926+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ11 as ready",
"entity_name": "KCNJ11",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:50:07.563805+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj11 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ11",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:41:57.575352+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH3 as ready",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:41:57.559504+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh3 has been classified as Red List (Low Evidence).",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:41:38.457609+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHKB as ready",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:41:38.446028+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phkb has been classified as Red List (Low Evidence).",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:04:00.273447+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHKB were set to ",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:03:31.520812+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKAG2 as ready",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:03:31.510607+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkag2 has been classified as Red List (Low Evidence).",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:03:09.496279+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A20 as ready",
"entity_name": "SLC25A20",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:03:09.485788+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a20 has been classified as Red List (Low Evidence).",
"entity_name": "SLC25A20",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:02:41.368053+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SUCLA2 as ready",
"entity_name": "SUCLA2",
"entity_type": "gene"
},
{
"created": "2020-10-07T21:02:41.357475+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sucla2 has been classified as Red List (Low Evidence).",
"entity_name": "SUCLA2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:59:49.713404+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN54 as ready",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:59:49.701638+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen54 has been classified as Red List (Low Evidence).",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:59:39.341930+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN54 were set to ",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:59:16.641406+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSFM as ready",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:59:16.633553+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsfm has been classified as Red List (Low Evidence).",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:58:56.379321+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSFM were set to ",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:58:19.905339+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTN as ready",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:58:19.896579+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttn has been classified as Red List (Low Evidence).",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:57:52.701786+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TYMP as ready",
"entity_name": "TYMP",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:57:52.691502+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tymp has been classified as Red List (Low Evidence).",
"entity_name": "TYMP",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:57:43.421815+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TYMP were set to ",
"entity_name": "TYMP",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:56:57.161281+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGM1 as ready",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:56:57.152122+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgm1 has been classified as Green List (High Evidence).",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:56:48.730276+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGM1 were changed from Congenital disorder of glycosylation, type It 614921 to Congenital disorder of glycosylation, type It, MIM# 614921",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:56:23.411290+11:00",
"panel_name": "Rhabdomyolysis RMH",
"panel_id": 3084,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGM1 were set to ",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:41:29.820493+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPC3 as ready",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:41:29.805975+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:40:51.362517+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TWIST1 as ready",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:40:51.353527+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: twist1 has been classified as Green List (High Evidence).",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:40:48.874108+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TWIST1 were changed from to Craniosynostosis 1, MIM# 123100; Saethre-Chotzen syndrome with or without eyelid anomalies, MIM# 101400",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:40:22.305167+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TWIST1 were set to ",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:39:55.005719+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TWIST1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:39:28.859224+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: TWIST1.\nTag 5'UTR tag was added to gene: TWIST1.",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:39:17.630281+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TWIST1: Changed publications: 17343269, 9585583, 12116251, 31299755, 30040876",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:37:26.108421+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TWIST1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17343269, 9585583, 12116251; Phenotypes: Craniosynostosis 1, MIM# 123100, Saethre-Chotzen syndrome with or without eyelid anomalies, MIM# 101400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:34:45.487370+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RUNX2 as ready",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:34:45.476407+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: runx2 has been classified as Green List (High Evidence).",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:34:42.974786+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RUNX2 were changed from to Craniosynostosis",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:33:01.887623+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RUNX2 were set to ",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:32:32.679967+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: RUNX2.",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:32:27.341164+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RUNX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:31:58.507796+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RUNX2: Rating: GREEN; Mode of pathogenicity: Other; Publications: 32360898, 23348268, 23307468; Phenotypes: Craniosynostosis; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:28:38.803216+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RECQL4 as ready",
"entity_name": "RECQL4",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:28:38.792404+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: recql4 has been classified as Green List (High Evidence).",
"entity_name": "RECQL4",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:28:35.971436+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RECQL4 were changed from to Baller-Gerold syndrome, MIM# 218600",
"entity_name": "RECQL4",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:28:07.661787+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RECQL4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RECQL4",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:27:38.856754+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RECQL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Baller-Gerold syndrome, MIM# 218600; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RECQL4",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:18:12.645760+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POR as ready",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:18:12.636326+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: por has been classified as Green List (High Evidence).",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:18:07.489802+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POR were changed from to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM# 201750",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:17:36.927403+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POR were set to ",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:17:09.885675+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: POR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:16:41.636904+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: POR: Rating: GREEN; Mode of pathogenicity: None; Publications: 26969897, 26670660, 18259105; Phenotypes: Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM# 201750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:13:30.520118+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MSX2 as ready",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:13:30.510303+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: msx2 has been classified as Green List (High Evidence).",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:13:27.456839+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MSX2 were changed from to Craniosynostosis 2, MIM# 604757",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:13:00.716204+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MSX2 were set to ",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:12:30.339943+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MSX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:12:00.274743+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MSX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23949913, 27884935, 23918290, 2359311, 22948472, 19533795; Phenotypes: Craniosynostosis 2, MIM# 604757; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSX2",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:07:40.514617+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL11RA as ready",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:07:40.504398+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il11ra has been classified as Green List (High Evidence).",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:07:31.218723+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL11RA were changed from to Craniosynostosis and dental anomalies, MIM# 614188",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:07:13.480342+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL11RA were set to ",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:06:44.489533+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL11RA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:06:27.340157+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL11RA: Rating: GREEN; Mode of pathogenicity: None; Publications: 21741611, 32277509, 30811827, 29926465, 24498618; Phenotypes: Craniosynostosis and dental anomalies, MIM# 614188; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:05:19.547388+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL11RA as ready",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:05:19.537225+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il11ra has been classified as Green List (High Evidence).",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:05:12.856789+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL11RA were changed from to Craniosynostosis and dental anomalies, MIM# 614188",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:04:45.357520+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL11RA were set to ",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:04:15.606174+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL11RA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T20:03:45.356209+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL11RA: Rating: GREEN; Mode of pathogenicity: None; Publications: 21741611, 32277509, 30811827, 29926465, 24498618; Phenotypes: Craniosynostosis and dental anomalies, MIM# 614188; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL11RA",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:56:23.012120+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGFR3 as ready",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:56:23.003222+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr3 has been classified as Green List (High Evidence).",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:08:46.969762+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGFR3 were changed from to Crouzon syndrome with acanthosis nigricans, MIM# 612247; Muenke syndrome, MIM# 602849",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:08:20.889807+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: FGFR3 was changed from to Other",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:07:52.234848+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGFR3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:07:25.719090+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGFR3: Rating: GREEN; Mode of pathogenicity: Other; Publications: ; Phenotypes: Crouzon syndrome with acanthosis nigricans, MIM# 612247, Muenke syndrome, MIM# 602849; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:05:48.758372+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGFR2 as ready",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:05:48.747770+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr2 has been classified as Green List (High Evidence).",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:05:34.322934+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGFR2 were changed from to Apert syndrome, MIM# 101200; Crouzon syndrome, MIM# 123500; Pfeiffer syndrome, MIM# 101600; Saethre-Chotzen syndrome, MIM# 101400",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:05:06.721000+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: FGFR2 was changed from to Other",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:04:06.537036+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGFR2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T19:03:38.321475+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGFR2: Rating: GREEN; Mode of pathogenicity: Other; Publications: ; Phenotypes: Apert syndrome, MIM# 101200, Crouzon syndrome, MIM# 123500, Pfeiffer syndrome, MIM# 101600, Saethre-Chotzen syndrome, MIM# 101400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:51:52.782988+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZIC1 as ready",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:51:52.775499+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zic1 has been classified as Green List (High Evidence).",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:51:34.030807+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC1 were changed from to Structural brain anomalies with impaired intellectual development and craniosynostosis, MIM# 618736; Craniosynostosis 6, MIM# 616602",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:51:07.433611+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZIC1 were set to ",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:50:45.911969+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZIC1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:50:14.873713+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZIC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26340333, 32975022, 27884935; Phenotypes: Structural brain anomalies with impaired intellectual development and craniosynostosis, MIM# 618736, Craniosynostosis 6, MIM# 616602; Mode of inheritance: None",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:47:09.949221+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGFR1 as ready",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:47:09.940252+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr1 has been classified as Green List (High Evidence).",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:47:07.415480+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGFR1 were changed from to Pfeiffer syndrome, MIM# 101600; Jackson-Weiss syndrome 123150",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:46:39.342156+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: FGFR1 was changed from to Other",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:46:12.782087+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGFR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2020-10-07T17:45:44.402352+11:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGFR1: Rating: GREEN; Mode of pathogenicity: Other; Publications: ; Phenotypes: Pfeiffer syndrome, MIM# 101600, Jackson-Weiss syndrome 123150; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR1",
"entity_type": "gene"
}
]
}