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{
"count": 220751,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=749",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=747",
"results": [
{
"created": "2022-09-21T19:00:23.367742+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ank1 has been classified as Red List (Low Evidence).",
"entity_name": "ANK1",
"entity_type": "gene"
},
{
"created": "2022-09-21T19:00:03.892055+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ANK1: Changed rating: RED",
"entity_name": "ANK1",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:59:49.695398+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ANK1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spherocytosis, type 1 MIM#182900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ANK1",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:57:46.337970+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AMT as ready",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:57:46.329197+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: amt has been classified as Red List (Low Evidence).",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:57:40.948466+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AMT were changed from Hyperglycinaemia, non-ketotic to Glycine encephalopathy MIM#605899",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:48:27.012035+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AMT as Red List (low evidence)",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:48:27.000273+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: amt has been classified as Red List (Low Evidence).",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:48:02.189756+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: AMT: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Glycine encephalopathy MIM#605899; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:44:40.855713+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: AMN: Changed phenotypes: Megaloblastic anaemia-1, Norwegian type, MIM#618882",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:44:24.699848+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AMN as ready",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:44:24.688729+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: amn has been classified as Green List (High Evidence).",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:44:14.332272+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: AMN.",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:44:00.082039+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.\r\n\r\nImerslund-Grasbeck syndrome-2 (IGS2) is an autosomal recessive disorder characterized by onset of megaloblastic anaemia associated with decreased serum vitamin B12 (cobalamin, Cbl) in infancy or early childhood.; to: Well established gene-disease association.\r\n\r\nImerslund-Grasbeck syndrome-2 (IGS2) is an autosomal recessive disorder characterized by onset of megaloblastic anaemia associated with decreased serum vitamin B12 (cobalamin, Cbl) in infancy or early childhood.\r\n\r\nClinical features include failure to thrive, loss of appetite, fatigue, lethargy, and/or recurrent infections.\r\n\r\nTreatment: cobalamin.",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:43:29.264593+10:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: AMN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AMN",
"entity_type": "gene"
},
{
"created": "2022-09-21T18:42:27.864549+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.345",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Cataract, HP:0000518\nList of related panels changed from to Cataract; HP:0000518",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:41:26.349875+10:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Cardiomyopathy, HP:0001638\nList of related panels changed from to Cardiomyopathy; HP:0001638",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:40:58.522439+10:00",
"panel_name": "Cardiomyopathy_Adult_SuperPanel",
"panel_id": 253,
"panel_version": "1.39",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Cardiomyopathy, HP:0001638\nList of related panels changed from to Cardiomyopathy; HP:0001638",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:40:12.937415+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.463",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Abnormal corpus callosum morphology, HP:0001273\nList of related panels changed from to Abnormal corpus callosum morphology; HP:0001273",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:37:35.733924+10:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "1.15",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Cerebral calcification, HP:0002514\nList of related panels changed from to Cerebral calcification; HP:0002514",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:33:46.794561+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "1.20",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Abnormality of multiple cell lineages of the bone marrow, HP:0012145\nList of related panels changed from to Abnormality of multiple cell lineages of the bone marrow; HP:0012145",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:32:04.289090+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Blepharophimosis, HP:0000581\nList of related panels changed from to Blepharophimosis; HP:0000581",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T18:30:57.823180+10:00",
"panel_name": "Bleeding and Platelet Disorders",
"panel_id": 54,
"panel_version": "1.16",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Abnormal bleeding, HP:0001892;Abnormal thrombosis, HP:0001977\nList of related panels changed from to Abnormal bleeding; HP:0001892;Abnormal thrombosis; HP:0001977",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:22:16.011922+10:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Autism, HP:0000717\nList of related panels changed from to Autism; HP:0000717",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:20:31.772232+10:00",
"panel_name": "Atrial Fibrillation",
"panel_id": 210,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Atrial fibrillation, HP:0005110\nList of related panels changed from to Atrial fibrillation; HP:0005110",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:19:02.189502+10:00",
"panel_name": "Ataxia - paediatric",
"panel_id": 271,
"panel_version": "0.344",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Ataxia; HP:0001251",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:18:02.822602+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Flexion contracture; HP:0001371",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:17:10.690011+10:00",
"panel_name": "Arrhythmogenic Cardiomyopathy",
"panel_id": 48,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "HPO terms changed from to Arrhythmia, HP:0011675;Cardiomyopathy, HP:0001638\nList of related panels changed from to Arrhythmia; HP:0011675;Cardiomyopathy; HP:0001638",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:15:32.427890+10:00",
"panel_name": "Aortopathy_Connective Tissue Disorders",
"panel_id": 44,
"panel_version": "1.72",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Aortic aneurysm; HP:0004942;Joint dislocation; HP:0001373;Cutis laxa; HP:0000973; Ectopia lentis; HP:0001083;Arachnodactyly; HP:0001166",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:14:48.314137+10:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.30",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Anophthalmia; HP:0000528;Microphthalmia; HP:0000568;Coloboma; HP:0000589",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:14:04.150437+10:00",
"panel_name": "Amelogenesis imperfecta",
"panel_id": 3564,
"panel_version": "1.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Amelogenesis imperfecta; HP:0000705",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:12:48.457243+10:00",
"panel_name": "Alternating Hemiplegia and Hemiplegic Migraine",
"panel_id": 40,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Hemiplegia; HP:0002301;Migraine; HP:0002076",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T17:10:56.297254+10:00",
"panel_name": "Achromatopsia",
"panel_id": 3149,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "List of related panels changed from to Achromatopsia; HP:0011516",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:58:42.488065+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TRPS1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:58:05.301418+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TTC8 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:54:08.727149+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TYROBP from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:53:40.074342+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:USP9X from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:51:49.442577+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TWIST1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:51:17.918447+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:UBA2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:50:44.516661+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TNFSF11 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:50:16.496337+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TNFRSF11B from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:49:49.859717+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TONSL from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:49:24.757990+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TP63 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:48:45.230936+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT5A as ready",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:48:45.218518+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt5a has been classified as Green List (High Evidence).",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:48:39.654339+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WNT5A as Green List (high evidence)",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:48:39.646040+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt5a has been classified as Green List (High Evidence).",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:48:03.089327+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:WNT10B from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:47:22.201648+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:VDR from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:46:31.934459+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:WISP3 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:46:03.912122+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:WNT7A from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:43:56.179069+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:XRCC4 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:43:06.845614+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XYLT1 as ready",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:43:06.835607+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xylt1 has been classified as Green List (High Evidence).",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:43:02.575411+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XYLT1 as Green List (high evidence)",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:43:02.567069+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xylt1 has been classified as Green List (High Evidence).",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:42:23.621163+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:XYLT2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:41:51.468177+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:YY1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:34:23.938686+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZMPSTE24 as ready",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:34:23.927275+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmpste24 has been classified as Green List (High Evidence).",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:34:18.845702+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZMPSTE24 as Green List (high evidence)",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:34:18.836388+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmpste24 has been classified as Green List (High Evidence).",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:33:15.289501+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZSWIM6 as ready",
"entity_name": "ZSWIM6",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:33:15.275367+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zswim6 has been classified as Green List (High Evidence).",
"entity_name": "ZSWIM6",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:33:05.643252+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZSWIM6 as Green List (high evidence)",
"entity_name": "ZSWIM6",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:33:05.633588+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zswim6 has been classified as Green List (High Evidence).",
"entity_name": "ZSWIM6",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:32:11.143701+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:WDPCP from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:31:34.582887+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:UFSP2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:30:58.110400+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TRAPPC2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:30:33.797868+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TREM2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-09-21T16:28:22.313388+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPS1 as ready",
"entity_name": "TRPS1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:28:22.304519+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trps1 has been classified as Red List (Low Evidence).",
"entity_name": "TRPS1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:28:18.385806+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRPS1 as Red List (low evidence)",
"entity_name": "TRPS1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:28:18.375993+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trps1 has been classified as Red List (Low Evidence).",
"entity_name": "TRPS1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:27:47.013001+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRPS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TRPS1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:26:57.206986+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:26:57.187085+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Red List (Low Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:26:35.065402+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC8 as Red List (low evidence)",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:26:35.056594+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Red List (Low Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:26:07.705366+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:24:41.782004+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TWIST1 as ready",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:24:41.772753+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: twist1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:24:14.053664+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TWIST1 as Amber List (moderate evidence)",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:24:14.045997+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: twist1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:23:51.070633+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: TWIST1.",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:23:42.362689+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TWIST1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:22:41.055082+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TYROBP as ready",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:22:41.046418+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tyrobp has been classified as Red List (Low Evidence).",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:21:01.501674+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TYROBP as Red List (low evidence)",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-09-21T16:21:01.492291+10:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tyrobp has been classified as Red List (Low Evidence).",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:36:02.705154+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ALPL: Rating: GREEN; Mode of pathogenicity: None; Publications: 31413732, 30811537; Phenotypes: Hypophosphatasia, adult 146300 (AD, AR), Hypophosphatasia, childhood 241510 AR, Hypophosphatasia, infantile 241500 AR, Odontohypophosphatasia 146300 AD, AR; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:35:31.626091+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALPL as ready",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:35:31.616603+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alpl has been classified as Green List (High Evidence).",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:35:21.230557+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALPL were changed from hypophosphatasia; Osteogenesis Imperfecta and Decreased Bone Density; skeletal dysplasias to Hypophosphatasia, adult 146300 (AD, AR); Hypophosphatasia, childhood 241510 AR; Hypophosphatasia, infantile 241500 AR; Odontohypophosphatasia 146300 AD, AR",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:34:52.874724+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALPL were set to ",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:34:00.651378+10:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ALPL.",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:33:20.966031+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ALPL.",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:32:54.197152+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ALPL.",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:32:27.477849+10:00",
"panel_name": "Hypophosphataemic Rickets",
"panel_id": 122,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ALPL.",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2022-09-21T11:32:01.327551+10:00",
"panel_name": "Craniosynostosis",
"panel_id": 93,
"panel_version": "1.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ALPL.",
"entity_name": "ALPL",
"entity_type": "gene"
}
]
}