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"count": 220790,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1982",
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"results": [
{
"created": "2020-01-16T10:05:05.451206+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TET3 as Green List (high evidence)",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:05:05.443808+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tet3 has been classified as Green List (High Evidence).",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:04:44.015466+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TET3 was added\ngene: TET3 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: TET3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: TET3 were set to 31928709\nPhenotypes for gene: TET3 were set to Intellectual disability; dysmorphic features; abnormal growth; movement disorders\nReview for gene: TET3 was set to GREEN\nAdded comment: Eleven individuals from 8 families described. Mono-allelic frameshift and nonsense variants occur throughout the coding region. Mono-allelic and bi-allelic missense variants localize to conserved residues; all but one such variant occur within the catalytic domain, and most display hypomorphic function in an assay of catalytic activity. \nSources: Literature",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:02:21.598402+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.796",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T10:00:52.062059+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1599",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TET3 as ready",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:00:52.054789+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1599",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tet3 has been classified as Green List (High Evidence).",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:00:09.896912+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1599",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TET3 as Green List (high evidence)",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T10:00:09.889399+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1599",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tet3 has been classified as Green List (High Evidence).",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T09:59:32.028089+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1598",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TET3 was added\ngene: TET3 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: TET3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: TET3 were set to 31928709\nPhenotypes for gene: TET3 were set to Intellectual disability; dysmorphic features; abnormal growth; movement disorders\nReview for gene: TET3 was set to GREEN\nAdded comment: Eleven individuals from 8 families described. Mono-allelic frameshift and nonsense variants occur throughout the coding region. Mono-allelic and bi-allelic missense variants localize to conserved residues; all but one such variant occur within the catalytic domain, and most display hypomorphic function in an assay of catalytic activity. \nSources: Literature",
"entity_name": "TET3",
"entity_type": "gene"
},
{
"created": "2020-01-16T09:18:05.589475+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:15:55.746874+11:00",
"panel_name": "Channelopathy",
"panel_id": 74,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:15:07.052530+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:13:03.157128+11:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Cerebellar and Pontocerebellar hypoplasia to Cerebellar and Pontocerebellar Hypoplasia\nPanel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:12:16.597941+11:00",
"panel_name": "Central Hypoventilation",
"panel_id": 71,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:11:29.421288+11:00",
"panel_name": "Catecholaminergic Polymorphic Ventricular Tachycardia",
"panel_id": 92,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T09:10:39.618533+11:00",
"panel_name": "Cardiomyopathy_SuperPanel",
"panel_id": 253,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Superpanel; Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T07:13:14.423958+11:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Australian Genomics; Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-16T07:12:30.866627+11:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Lissencephaly and band heterotopia to Lissencephaly and Band Heterotopia",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:48:46.453233+11:00",
"panel_name": "Renal Tubulointerstitial Disease",
"panel_id": 199,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; KidGen; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:46:58.253098+11:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; KidGen; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:45:56.025292+11:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; KidGen; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:41:04.051310+11:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:40:10.847937+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:38:58.216036+11:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:36:06.878188+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Brain calcification to Brain Calcification\nPanel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:35:12.806870+11:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:34:27.473788+11:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:33:37.173646+11:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:31:42.122672+11:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:30:52.267219+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:30:10.789967+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN",
"panel_id": 211,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; KidGen; Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:28:52.039605+11:00",
"panel_name": "Atrial Fibrillation",
"panel_id": 210,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Atrial fibrillation to Atrial Fibrillation\nPanel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:17:25.197830+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:16:42.303365+11:00",
"panel_name": "Arrhythmogenic Right Ventricular Cardiomyopathy",
"panel_id": 48,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:14:06.940489+11:00",
"panel_name": "Arrhythmia_SuperPanel",
"panel_id": 254,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Superpanel; Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:12:59.720970+11:00",
"panel_name": "Aortopathy_Connective Tissue Disorders",
"panel_id": 44,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Aortopathy_Connective tissue disorders to Aortopathy_Connective Tissue Disorders\nPanel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:12:02.195671+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:10:49.345275+11:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:09:24.281697+11:00",
"panel_name": "Alternating Hemiplegia and Hemiplegic Migraine",
"panel_id": 40,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T20:05:46.295335+11:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T19:23:30.790953+11:00",
"panel_name": "Severe Combined Immunodeficiency (absent T present B cells)",
"panel_id": 235,
"panel_version": "0.6",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Severe Combined Immunodeficiency (absent T, present B cells) to Severe Combined Immunodeficiency (absent T present B cells)",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T19:22:40.632871+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1596",
"user_name": "Sebastian Lunke",
"item_type": "panel",
"text": "Panel name changed from Intellectual disability, syndromic and non-syndromic to Intellectual disability syndromic and non-syndromic",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T18:05:20.621108+11:00",
"panel_name": "Alternating Hemiplegia and Hemiplegic Migraine",
"panel_id": 40,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Alternating hemiplegia including hemiplegic migraine to Alternating Hemiplegia and Hemiplegic Migraine",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:57:35.055675+11:00",
"panel_name": "Storage Disorder",
"panel_id": 181,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Storage Disorder_VCGS to Storage Disorder\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:53:48.454235+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Skeletal dysplasia Fetal_MelbourneGenomics_VCGS to Skeletal Dysplasia_Fetal\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:51:23.516159+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:47:40.987859+11:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy",
"panel_id": 179,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS to Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:46:34.995753+11:00",
"panel_name": "Short QT syndrome",
"panel_id": 174,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Short QT syndrome_VCGS to Short QT syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:44:52.644429+11:00",
"panel_name": "Severe Combined Immunodeficiency (absent T, present B cells)",
"panel_id": 235,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Severe combined immunodeficiency (absent T, present B cells)_MelbourneGenomics_VCGS to Severe Combined Immunodeficiency (absent T, present B cells)\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:36:47.995871+11:00",
"panel_name": "Renal Tubulointerstitial Disease",
"panel_id": 199,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal tubulointerstitial disease_KidGen_VCGS to Renal Tubulointerstitial Disease\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:34:17.338315+11:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal macrocystic disease_KidGen_VCGS to Renal Macrocystic Disease\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:33:17.157719+11:00",
"panel_name": "Renal Hypertension and Disorders of Aldosterone Metabolism",
"panel_id": 190,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS to Renal Hypertension and Disorders of Aldosterone Metabolism\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:31:55.069687+11:00",
"panel_name": "Renal Glomerular Disease_SuperPanel",
"panel_id": 262,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal glomerular disease_SuperPanel_VCGS_KidGen to Renal Glomerular Disease_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:31:22.048654+11:00",
"panel_name": "Renal Cystic Disease_SuperPanel",
"panel_id": 263,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal cystic disease_SuperPanel_KidGen_VCGS to Renal Cystic Disease_SuperPanel\nPanel types changed to Superpanel; Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:31:01.060269+11:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal ciliopathies and nephronophthisis_KidGen_VCGS to Renal Ciliopathies and Nephronophthisis\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:30:03.200495+11:00",
"panel_name": "Renal Amyloidosis",
"panel_id": 191,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal amyloidosis_KidGen_VCGS to Renal Amyloidosis\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:25:11.524011+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Regression_VCGS to Regression\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:24:23.589154+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Rasopathy_VCGS to Rasopathy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:23:19.402349+11:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Radial Ray Abnormalities_VCGS to Radial Ray Abnormalities\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:22:16.925151+11:00",
"panel_name": "Pulmonary Fibrosis_Interstitial Lung Disease",
"panel_id": 162,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Pulmonary Fibrosis_VCGS to Pulmonary Fibrosis_Interstitial Lung Disease\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:21:14.855763+11:00",
"panel_name": "Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy",
"panel_id": 161,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Pseudohypoparathyroidism, Albright Hereditary Osteodystrophy_VCGS to Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:19:49.650897+11:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Proteinuria_VCGS_KidGen to Proteinuria\nPanel types changed to Victorian Clinical Genetics Services; KidGen",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:18:51.316389+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Predominantly antibody deficiency_MelbourneGenomics_VCGS to Predominantly Antibody Deficiency\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:17:09.107470+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Polymicrogyria and schizencephaly_AustralianGenomics_VCGS to Polymicrogyria and Schizencephaly\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:14:02.744036+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALMS1 as ready",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:14:02.734838+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alms1 has been classified as Red List (Low Evidence).",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:13:59.064610+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALMS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:13:27.211142+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALMS1 were changed from to Alstrom syndrome, MIM#203800",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:13:01.696124+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALMS1 as Red List (low evidence)",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:13:01.688379+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alms1 has been classified as Red List (Low Evidence).",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:12:25.332570+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ALMS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Alstrom syndrome, MIM#203800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-01-15T17:10:49.409675+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Polydactyly_VCGS to Polydactyly\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:09:28.586034+11:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Pierre Robin sequence _VCGS to Pierre Robin Sequence\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:08:34.017640+11:00",
"panel_name": "Photosensitivity Syndromes",
"panel_id": 156,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Photosensitivity syndromes_VCGS to Photosensitivity Syndromes\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:07:22.841526+11:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Phagocyte defects_MelbourneGenomics_VCGS to Phagocyte Defects\nPanel types changed to Victorian Clinical Genetics Services; Melbourne Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:06:02.912398+11:00",
"panel_name": "Peroxisomal Disorders",
"panel_id": 155,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Peroxisomal Disorders_VCGS to Peroxisomal Disorders\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:05:07.082925+11:00",
"panel_name": "Periventricular Grey Matter Heterotopia",
"panel_id": 19,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Periventricular grey matter heterotopia_AustralianGenomics_VCGS to Periventricular Grey Matter Heterotopia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:03:48.081301+11:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Paroxysmal dyskinesia_VCGS to Paroxysmal Dyskinesia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:03:02.537331+11:00",
"panel_name": "Pancreatitis",
"panel_id": 154,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Pancreatitis_VCGS to Pancreatitis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:02:17.951798+11:00",
"panel_name": "Palmoplantar Keratoderma and Erythrokeratoderma",
"panel_id": 153,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Palmoplantar keratoderma and erythrokeratoderma_VCGS to Palmoplantar Keratoderma and Erythrokeratoderma\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:01:22.380061+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Overgrowth_VCGS to Overgrowth\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T17:00:28.716547+11:00",
"panel_name": "Osteopetrosis",
"panel_id": 150,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Osteopetrosis_VCGS to Osteopetrosis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:59:42.681035+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Osteogenesis imperfecta_VCGS to Osteogenesis Imperfecta\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:58:55.223194+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Optic Atrophy_VCGS to Optic Atrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:58:10.519574+11:00",
"panel_name": "Oligodontia",
"panel_id": 148,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Oligodontia_VCGS to Oligodontia\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:57:19.197837+11:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Ocular and oculocutaneous albinism_VCGS to Ocular and Oculocutaneous Albinism\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:54:25.906484+11:00",
"panel_name": "Neurotransmitter Defects",
"panel_id": 145,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Neurotransmitter Defect_VCGS to Neurotransmitter Defects\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:53:22.741655+11:00",
"panel_name": "Motor Neuron Disease",
"panel_id": 25,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Motor neuron disease_MND to Motor Neuron Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:47:38.986506+11:00",
"panel_name": "Arrhythmogenic Right Ventricular Cardiomyopathy",
"panel_id": 48,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Arrhythmogenic right ventricular cardiomyopathy_ARVC to Arrhythmogenic Right Ventricular Cardiomyopathy",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:45:47.056461+11:00",
"panel_name": "Catecholaminergic Polymorphic Ventricular Tachycardia",
"panel_id": 92,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Catecholaminergic polymorphic ventricular tachycardia_CPVT to Catecholaminergic Polymorphic Ventricular Tachycardia",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:44:06.982938+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Dilated cardiomyopathy_DCM to Dilated Cardiomyopathy",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T16:36:44.016007+11:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Brugada syndrome_VCGS to Brugada syndrome",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:43:00.782912+11:00",
"panel_name": "Muscular dystrophy",
"panel_id": 141,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Muscular dystrophy_VCGS to Muscular dystrophy\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:42:01.922256+11:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Multiple pterygium syndromeVCGS to Multiple pterygium syndrome\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:41:19.971486+11:00",
"panel_name": "Motor neuron disease_MND",
"panel_id": 25,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Motor neuron disease MND_MelbourneGenomics_VCGS to Motor neuron disease_MND\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:40:33.792687+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Mitochondrial_AustralianGenomics_VCGS to Mitochondrial disease\nPanel types changed to Victorian Clinical Genetics Services; Australian Genomics",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:38:08.092676+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Microcephaly_VCGS to Microcephaly\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:37:30.113090+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.795",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Mendeliome_VCGS to Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:35:31.384999+11:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Mandibulofacial Acrofacial dysostosis_VCGS to Mandibulofacial Acrofacial dysostosis\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T15:34:56.943013+11:00",
"panel_name": "Macrocephaly_Megalencephaly",
"panel_id": 135,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Macrocephaly/Megalencephaly_VCGS to Macrocephaly_Megalencephaly\nPanel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
}
]
}