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{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1782",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1780",
"results": [
{
"created": "2020-06-01T14:43:15.683734+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ANK2 as ready",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:43:15.670815+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ank2 has been classified as Red List (Low Evidence).",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:42:32.251563+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ANK2 were changed from to Long QT syndrome 4, MIM#\t600919",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:42:31.834537+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2943",
"user_name": "Paul De Fazio",
"item_type": "entity",
"text": "gene: RIMS2 was added\ngene: RIMS2 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: RIMS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RIMS2 were set to 32470375\nReview for gene: RIMS2 was set to GREEN\nAdded comment: Segregates with Syndromic Congenital Cone-Rod Synaptic Disease in 7 individuals across 4 families. Some functional studies related to insulin secretion but they are non-significant. \nSources: Literature",
"entity_name": "RIMS2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:41:59.588275+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ANK2 were set to ",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:41:33.426233+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ANK2 as Red List (low evidence)",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:41:33.417138+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ank2 has been classified as Red List (Low Evidence).",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:41:00.794120+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ANK2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:40:19.759646+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.46",
"user_name": "Kristin Rigbye",
"item_type": "entity",
"text": "gene: SCYL2 was added\ngene: SCYL2 was added to Arthrogryposis. Sources: Literature\nMode of inheritance for gene: SCYL2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SCYL2 were set to 31960134; 26203146\nPhenotypes for gene: SCYL2 were set to Arthrogryposis multiplex congenita (AMC); Zain syndrome\nReview for gene: SCYL2 was set to AMBER\nAdded comment: 2 unrelated consanguineous families reported with AMC (PMID: 31960134).\r\nConstitutive mouse knockout of Scyl2 results in neonatal lethality and severe motor and sensory deficits (PMID: 26203146). \nSources: Literature",
"entity_name": "SCYL2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:40:07.508754+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: AKAP9.",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:39:51.775964+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AKAP9 as ready",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:39:51.763668+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap9 has been classified as Red List (Low Evidence).",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:39:48.987324+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AKAP9 were changed from to Long QT syndrome 11, MIM# 611820",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:39:18.118243+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: AKAP9 were set to ",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:38:50.086386+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AKAP9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:38:27.007148+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AKAP9 as Red List (low evidence)",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:38:26.993337+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap9 has been classified as Red List (Low Evidence).",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:37:54.050849+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: AKAP9: Rating: RED; Mode of pathogenicity: None; Publications: 31983240; Phenotypes: Long QT syndrome 11, MIM# 611820; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:36:35.201730+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: AKAP9.",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:36:12.342786+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AKAP9 as ready",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:36:12.321710+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap9 has been classified as Red List (Low Evidence).",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:36:07.049288+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AKAP9 were changed from to long QT syndrome",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:35:36.796124+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: AKAP9 were set to ",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:35:06.582765+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AKAP9 as Red List (low evidence)",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:35:06.573497+10:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap9 has been classified as Red List (Low Evidence).",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:34:31.936900+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2943",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: RBM7 as Amber List (moderate evidence)",
"entity_name": "RBM7",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:34:31.927473+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2943",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: rbm7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RBM7",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:34:09.964599+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2942",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: RBM7 was added\ngene: RBM7 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: RBM7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RBM7 were set to 27193168\nPhenotypes for gene: RBM7 were set to SMA-like spinal motor neuropathy; dHMN/dSMA\nReview for gene: RBM7 was set to AMBER\nAdded comment: Single case with a homozygote variant, with functional assays in patient fibroblasts. Also, supporting zebrafish model. \nSources: Expert list",
"entity_name": "RBM7",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:33:50.405813+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2941",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: SORD as ready",
"entity_name": "SORD",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:33:50.396827+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2941",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: sord has been classified as Green List (High Evidence).",
"entity_name": "SORD",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:33:35.723753+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2941",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Classified gene: SORD as Green List (high evidence)",
"entity_name": "SORD",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:33:35.709827+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2941",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: sord has been classified as Green List (High Evidence).",
"entity_name": "SORD",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:30:13.784984+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2940",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: SORD was added\ngene: SORD was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: SORD was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SORD were set to 32367058\nPhenotypes for gene: SORD were set to isolated hereditary neuropathy\nReview for gene: SORD was set to GREEN\ngene: SORD was marked as current diagnostic\nAdded comment: 45 individuals from 38 families across multiple ancestries carrying the nonsense c.757delG\r\n(p.Ala253GlnfsTer27) variant in SORD, in either a homozygous or compound heterozygous state \nSources: Literature",
"entity_name": "SORD",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:29:09.196250+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCND3 were changed from to Brugada syndrome",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:28:34.659112+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCND3.",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:28:10.927324+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CACNB2.",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:27:16.417641+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CACNA2D1.",
"entity_name": "CACNA2D1",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:26:48.471637+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CACNA1C.",
"entity_name": "CACNA1C",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:25:58.238600+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPD1L as Red List (low evidence)",
"entity_name": "GPD1L",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:25:58.229760+10:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpd1l has been classified as Red List (Low Evidence).",
"entity_name": "GPD1L",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:24:26.988930+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPD1L were set to 17967977; 19666841",
"entity_name": "GPD1L",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:23:51.349689+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GPD1L as Red List (low evidence)",
"entity_name": "GPD1L",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:23:51.336113+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpd1l has been classified as Red List (Low Evidence).",
"entity_name": "GPD1L",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:22:00.715806+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCN1B as ready",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:22:00.706320+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn1b has been classified as Red List (Low Evidence).",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:21:53.157035+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SCN1B were set to ",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:21:11.901207+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCN1B as Red List (low evidence)",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:21:11.891719+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn1b has been classified as Red List (Low Evidence).",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:20:44.516087+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SCN1B.",
"entity_name": "SCN1B",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:20:09.697188+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCN10A as ready",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:20:09.684879+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn10a has been classified as Red List (Low Evidence).",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:18:53.390262+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCN10A were changed from to Brugada syndrome",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:18:19.000547+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SCN10A were set to ",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:17:48.822097+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCN10A as Red List (low evidence)",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:17:48.808079+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn10a has been classified as Red List (Low Evidence).",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:17:21.290259+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SCN10A.",
"entity_name": "SCN10A",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:16:44.505417+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ8 as ready",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:16:44.496112+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:16:31.711028+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCNJ8 were changed from to Brugada syndrome",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:16:12.424635+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNJ8 were set to ",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:15:54.279840+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KCNJ8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:15:35.891500+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2937",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNJ8 as Red List (low evidence)",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:15:35.882740+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2937",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:15:16.829543+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCNJ8.",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:14:04.033119+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KCNJ8: Rating: RED; Mode of pathogenicity: None; Publications: 29959160; Phenotypes: Brugada syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:12:39.155493+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCNJ8 were changed from to Brugada syndrome",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:12:02.637803+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ8 as ready",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:12:02.628684+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:11:58.671256+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCNJ8.",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:11:26.677137+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNE3 as ready",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:11:26.668308+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne3 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:11:11.994588+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCNE3 were changed from to Brugada syndrome",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:10:49.674619+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNE3 were set to ",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:10:31.778778+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2934",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KCNE3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:10:09.495323+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNJ8 were set to ",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:09:36.866700+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNJ8 as Red List (low evidence)",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:09:36.853208+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:56.765562+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNE3 as ready",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:56.756802+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne3 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:48.303545+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCNE3.",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:29.668436+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNE3 as Red List (low evidence)",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:29.655117+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne3 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:08:00.906028+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KCNE3: Rating: RED; Mode of pathogenicity: None; Publications: 29959160; Phenotypes: Brugada syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:07:58.633659+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNE3 were set to ",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:07:01.151678+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNE3 as Red List (low evidence)",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:07:01.138766+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne3 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:06:21.114468+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCND3 as ready",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:06:21.102703+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnd3 has been classified as Red List (Low Evidence).",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:06:17.019973+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCND3 were set to ",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:05:47.562288+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCND3 as Red List (low evidence)",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:05:47.548919+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnd3 has been classified as Red List (Low Evidence).",
"entity_name": "KCND3",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:05:10.520623+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNB2 as ready",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:05:10.508234+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacnb2 has been classified as Red List (Low Evidence).",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:05:08.243998+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CACNB2 were set to ",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:04:38.558644+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CACNB2 as Red List (low evidence)",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:04:38.548938+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacnb2 has been classified as Red List (Low Evidence).",
"entity_name": "CACNB2",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:03:49.225904+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNA2D1 as ready",
"entity_name": "CACNA2D1",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:03:49.212876+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna2d1 has been classified as Red List (Low Evidence).",
"entity_name": "CACNA2D1",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:03:38.614428+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CACNA2D1 were set to ",
"entity_name": "CACNA2D1",
"entity_type": "gene"
},
{
"created": "2020-06-01T14:03:08.719340+10:00",
"panel_name": "Brugada syndrome",
"panel_id": 60,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CACNA2D1 as Red List (low evidence)",
"entity_name": "CACNA2D1",
"entity_type": "gene"
}
]
}