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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1064",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1062",
"results": [
{
"created": "2022-01-04T13:11:46.464223+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GRM1 as Red List (low evidence)",
"entity_name": "GRM1",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:11:46.453059+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grm1 has been classified as Red List (Low Evidence).",
"entity_name": "GRM1",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:11:34.561998+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GRM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spinocerebellar ataxia, autosomal recessive 13 MIM#614831; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GRM1",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:09:29.591254+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GRHL2 were set to 25152456",
"entity_name": "GRHL2",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:07:52.200675+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GRHL2 as Green List (high evidence)",
"entity_name": "GRHL2",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:07:52.189945+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grhl2 has been classified as Green List (High Evidence).",
"entity_name": "GRHL2",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:07:26.171321+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GRHL2 were set to 25152456; 29499165",
"entity_name": "GRHL2",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:06:21.281076+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from Anemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950 to Anaemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:05:36.278036+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A38 were set to 19412178; 31338833",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:04:28.779453+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1784",
"user_name": "Daniel Flanagan",
"item_type": "entity",
"text": "reviewed gene: LRAT: Rating: RED; Mode of pathogenicity: None; Publications: 11381255, 18055821, 22570351, 17011878, 29973277, 24625443, 22559933, 31448181; Phenotypes: Leber congenital amaurosis 14 MIM#613341, Retinal dystrophy, early-onset severe MIM#613341, Retinitis pigmentosa, juvenile MIM#613341; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LRAT",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:03:23.822387+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC25A38 as Amber List (moderate evidence)",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:03:23.811559+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-01-04T13:03:11.674133+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: AMBER; Mode of pathogenicity: None; Publications: 34298585; Phenotypes: Anaemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:55:57.126925+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC17A5 were set to 10581036; 10947946; 33862140",
"entity_name": "SLC17A5",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:54:03.853965+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GREB1L as ready",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:54:03.844171+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: greb1l has been classified as Green List (High Evidence).",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:53:35.885183+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GREB1L were changed from Renal hypodysplasia/aplasia 3, 617805; renal agenesis to Renal hypodysplasia/aplasia 3, MIM#617805; renal agenesis",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:53:24.922698+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GREB1L were set to 29261186; 32378186; 31974414; 31424080; 29100091",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:53:04.154227+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GREB1L was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:52:55.267726+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GREB1L as Green List (high evidence)",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:52:55.258073+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: greb1l has been classified as Green List (High Evidence).",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:52:43.753671+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GREB1L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal hypodysplasia/aplasia 3, OMIM# 617805; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GREB1L",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:52:04.650636+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPX4 as ready",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:52:04.639910+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpx4 has been classified as Green List (High Evidence).",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:51:22.039196+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPX4 were changed from Spondylometaphyseal dysplasia, Sedaghatian type 250220 to Spondylometaphyseal dysplasia, Sedaghatian type MIM#250220",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:50:43.010645+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1779",
"user_name": "Daniel Flanagan",
"item_type": "entity",
"text": "reviewed gene: LIPN: Rating: RED; Mode of pathogenicity: None; Publications: 21439540; Phenotypes: Ichthyosis, congenital, autosomal recessive 8 (MIM#613943); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LIPN",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:50:37.388601+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPX4 were set to 24706940",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:49:59.388549+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPX4 as Green List (high evidence)",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:49:59.324188+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpx4 has been classified as Green List (High Evidence).",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:49:13.684761+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPX4 as ready",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:49:13.674047+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpx4 has been classified as Green List (High Evidence).",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:49:08.086941+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPX4 were changed from SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE to Spondylometaphyseal dysplasia, Sedaghatian type MIM#250220",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:48:42.243156+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPX4 were set to ",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:48:29.617734+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPX4 as Green List (high evidence)",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:48:29.606129+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpx4 has been classified as Green List (High Evidence).",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:47:53.829837+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPX4 as ready",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:47:53.820931+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpx4 has been classified as Green List (High Evidence).",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:47:46.721295+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPX4 were changed from to Spondylometaphyseal dysplasia, Sedaghatian type MIM#250220",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:46:25.786330+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10460",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPX4 were set to ",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:46:07.367783+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPX4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPX4",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:45:00.406927+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC12A6 were changed from Andermann syndrome; Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum; Intermediate CMT to Andermann syndrome; Agenesis of the corpus callosum with peripheral neuropathy, MIM#21800; Intermediate CMT",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:44:38.642009+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SLC12A6: Changed phenotypes: Andermann syndrome, Agenesis of the corpus callosum with peripheral neuropathy, MIM#21800, Intermediate CMT",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:43:29.098368+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPKOW as ready",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:43:29.082493+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpkow has been classified as Red List (Low Evidence).",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:43:22.883170+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPKOW as Red List (low evidence)",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:43:22.873567+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpkow has been classified as Red List (Low Evidence).",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:42:57.964622+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPKOW as ready",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:42:57.949050+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpkow has been classified as Red List (Low Evidence).",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:39:21.421498+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPKOW as Red List (low evidence)",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:39:21.411185+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpkow has been classified as Red List (Low Evidence).",
"entity_name": "GPKOW",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:38:25.881316+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: GPC6.",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:38:04.529715+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPC6 as ready",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:38:04.510140+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpc6 has been classified as Green List (High Evidence).",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:37:56.091526+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPC6 were set to ",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:37:41.603489+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GPC6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Omodysplasia 1, MIM#258315; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:37:11.417366+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPC6 as Green List (high evidence)",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:37:11.389813+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpc6 has been classified as Green List (High Evidence).",
"entity_name": "GPC6",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:36:21.979767+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GNA11 as ready",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:36:21.969736+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gna11 has been classified as Red List (Low Evidence).",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:36:17.067518+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GNA11 were changed from Congenital Hemangioma to Hypocalcemia, autosomal dominant 2 MIM#615361; Hypocalciuric hypercalcemia, type II MIM#145981; Congenital Haemangioma",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:36:01.253755+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GNA11 were set to 23802536; 23802516; 24823460; 26818911; 27334330",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:35:41.097897+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Post-natal presentation.; to: Post-natal presentation for calcium disorders.\r\n\r\nSomatic variants present in cutaneous haemangiomas, which can be of perinatal onset.",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:35:05.323408+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: GNA11: Changed publications: 34040639",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:32:05.032205+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GNA11 were set to ",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:31:53.583317+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: GNA11 was changed from to Other",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:31:42.112934+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GNA11 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:31:32.083536+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GNA11 as Red List (low evidence)",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:31:32.067516+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gna11 has been classified as Red List (Low Evidence).",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:31:20.013245+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GNA11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypocalcemia, autosomal dominant 2 MIM#615361, Hypocalciuric hypercalcemia, type II MIM#145981; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:30:21.593487+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GNA11 as ready",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:30:21.582287+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gna11 has been classified as Green List (High Evidence).",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:30:13.170597+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GNA11 were changed from to Hypocalcemia, autosomal dominant 2 MIM#615361; Hypocalciuric hypercalcemia, type II MIM#145981",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:29:45.130381+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GNA11 were set to ",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:26:02.404638+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: GNA11 was changed from to Other",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:25:44.961375+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GNA11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:24:33.016127+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXC2 as ready",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:24:33.005283+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc2 has been classified as Green List (High Evidence).",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:24:24.424318+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FOXC2 were changed from LYMPHEDEMA-DISTICHIASIS SYNDROME; HEREDITARY LYMPHEDEMA II to Lymphoedema-distichiasis syndrome, MIM# 153400",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:24:09.448515+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FOXC2 were set to ",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:23:55.608062+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Single individual reported with CDH, some supportive functional data. \nSources: Literature; to: Lymphoedema-distichiasis is an autosomal dominant disorder that classically presents as lymphoedema of the limbs and double rows of eyelashes (distichiasis). Other features that may present antenatally include cardiac defects, cleft palate, spinal extradural cysts, and CDH. Well established gene-disease association, multiple families reported.\r\nSources: Literature",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:23:01.164807+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: FOXC2: Changed rating: GREEN; Changed publications: 33461977, 27663689, 11078474, 11694548, 11371511; Changed phenotypes: Lymphoedema-distichiasis syndrome, MIM# 153400",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T12:01:37.692101+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GZF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33009817, 28475863; Phenotypes: Joint laxity, short stature, and myopia, MIM# 617662, Larsen-like syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GZF1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:56:59.546994+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GSC: Rating: GREEN; Mode of pathogenicity: None; Publications: 24290375; Phenotypes: Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities, MIM# 602471; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GSC",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:54:23.430189+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXC2 as ready",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:54:23.413294+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc2 has been classified as Green List (High Evidence).",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:54:15.782888+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FOXC2 were changed from to Lymphoedema-distichiasis syndrome, MIM# 153400",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:53:56.088613+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FOXC2 were set to ",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:53:36.993517+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FOXC2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:53:19.021185+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FOXC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11078474, 11694548, 11371511; Phenotypes: Lymphoedema-distichiasis syndrome, MIM# 153400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:46:42.541453+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10449",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GRM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22901947, 26308914, 31319223; Phenotypes: Spinocerebellar ataxia 44 MIM#617691, Spinocerebellar ataxia, autosomal recessive 13 MIM#614831; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GRM1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:38:59.192354+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GRM1: Rating: RED; Mode of pathogenicity: None; Publications: 22901947, 26308914; Phenotypes: Spinocerebellar ataxia, autosomal recessive 13 MIM#614831; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GRM1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:16:37.386954+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXC1 as ready",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:16:37.376236+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc1 has been classified as Green List (High Evidence).",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:16:29.599502+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FOXC1 were changed from AXENFELD-RIEGER SYNDROME TYPE 3; IRIDOGONIODYSGENESIS ANOMALY; PETERS ANOMALY to Axenfeld-Rieger syndrome, type 3, MIM# 602482",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:16:17.467505+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FOXC1 were set to 32720677",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:16:04.385317+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FOXC1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:15:50.424324+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: FOXC1: Added comment: ARS can present antenatally with congenital heart disease and umbilical defects.; Changed rating: GREEN; Changed publications: 30255586; Changed phenotypes: Axenfeld-Rieger syndrome, type 3, MIM# 602482; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:14:50.105739+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1762",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GRHL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27612988, 19415813, 25152456; Phenotypes: Ectodermal dysplasia/short stature syndrome MIM#616029; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GRHL2",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:13:56.133776+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2022-01-04T11:13:23.186360+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOLR1 as ready",
"entity_name": "FOLR1",
"entity_type": "gene"
}
]
}