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{
"count": 220313,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1441",
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"results": [
{
"created": "2021-01-17T21:49:54.512684+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h1e has been classified as Green List (High Evidence).",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:49:47.024383+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HIST1H1E were changed from to Rahman syndrome, MIM# 617537",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:49:12.886404+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIST1H1E were set to ",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:48:39.597674+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HIST1H1E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:48:08.027505+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HIST1H1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 28475857, 33270410, 31910894, 31400068; Phenotypes: Rahman syndrome, MIM# 617537; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:47:31.194298+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6076",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H1E as ready",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:47:31.184111+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6076",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h1e has been classified as Green List (High Evidence).",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:47:23.513838+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6076",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HIST1H1E were changed from to Rahman syndrome, MIM# 617537",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:47:20.104051+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H1E as ready",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:47:20.093360+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h1e has been classified as Green List (High Evidence).",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:46:59.844272+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6075",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIST1H1E were set to ",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:46:45.310411+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HIST1H1E were changed from to Rahman syndrome, MIM# 617537",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:46:40.583665+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6074",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HIST1H1E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:46:19.741514+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HIST1H1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 28475857, 33270410, 31910894, 31400068; Phenotypes: Rahman syndrome, MIM# 617537; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:46:13.550003+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIST1H1E were set to ",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:45:41.598904+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HIST1H1E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:45:09.447972+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HIST1H1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 28475857, 33270410, 31910894, 31400068; Phenotypes: Rahman syndrome, MIM# 617537; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HIST1H1E",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:41:28.209471+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTOR were set to ",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:40:59.765922+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MTOR: Changed publications: 27830187",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:40:09.058847+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTOR as ready",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:40:09.050208+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtor has been classified as Green List (High Evidence).",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:40:00.650450+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTOR were changed from to Smith-Kingsmore syndrome, MIM# 616638",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:39:31.862888+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MTOR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:39:02.683648+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MTOR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Smith-Kingsmore syndrome, MIM# 616638; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:37:44.552379+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTEN as ready",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:37:44.543490+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pten has been classified as Green List (High Evidence).",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:37:33.267218+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTEN were changed from to Cowden syndrome 1, MIM# 158350; Macrocephaly/autism syndrome, MIM# 605309",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:37:04.627733+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTEN were set to ",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:36:35.724906+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:36:05.958069+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTEN: Rating: GREEN; Mode of pathogenicity: None; Publications: 31433956, 31609537; Phenotypes: Cowden syndrome 1, MIM# 158350, Macrocephaly/autism syndrome, MIM# 605309; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:32:17.358029+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFIX as ready",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T21:32:17.348136+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfix has been classified as Green List (High Evidence).",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:44:07.051386+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFIX were changed from to Sotos syndrome 2, MIM# 614753; Malan syndrome",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:43:13.512567+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIX were set to 33034087; 29897170; 30548146; 25118028",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:42:53.838402+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIX were set to 33034087; 29897170; 30548146; 25118028",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:42:33.966952+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIX were set to ",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:40:44.797579+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIX was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:40:12.923849+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NFIX: Rating: GREEN; Mode of pathogenicity: None; Publications: 33034087, 29897170, 30548146, 25118028; Phenotypes: Sotos syndrome 2, MIM# 614753, Malan syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:36:04.405649+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NSD1 as ready",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:36:04.391653+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nsd1 has been classified as Green List (High Evidence).",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:36:01.222247+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NSD1 were changed from to Sotos syndrome 1, MIM# 117550",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:35:35.592537+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NSD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:35:09.613345+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: NSD1.",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:35:00.682449+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NSD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Sotos syndrome 1, MIM# 117550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NSD1",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:25:27.703907+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPC3 as ready",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:25:27.692498+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpc3 has been classified as Green List (High Evidence).",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:25:23.809347+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPC3 were changed from to Simpson-Golabi-Behmel syndrome, type 1, MIM# 312870",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:24:43.241904+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPC3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:24:15.112216+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GPC3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Simpson-Golabi-Behmel syndrome, type 1, MIM# 312870; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "GPC3",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:23:12.506210+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EED as ready",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:23:12.490127+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eed has been classified as Green List (High Evidence).",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:20:06.073906+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EED were changed from to Cohen-Gibson syndrome, MIM# 617561",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:19:42.303787+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6072",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EED were set to ",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:19:23.279781+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6071",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EED was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:19:01.078339+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6070",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EED: Rating: GREEN; Mode of pathogenicity: None; Publications: 25787343, 27193220, 27868325, 28229514; Phenotypes: Cohen-Gibson syndrome, MIM# 617561; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:18:16.148638+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EED as ready",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:18:16.140506+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eed has been classified as Green List (High Evidence).",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:18:07.739442+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EED were changed from to Cohen-Gibson syndrome, MIM# 617561",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:17:30.657004+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EED were set to ",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:16:55.620250+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EED was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:16:21.911471+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EED: Rating: GREEN; Mode of pathogenicity: None; Publications: 25787343, 27193220, 27868325, 28229514; Phenotypes: Cohen-Gibson syndrome, MIM# 617561; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:16:01.974339+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EED as ready",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:16:01.954080+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eed has been classified as Green List (High Evidence).",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:15:34.091801+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EED were changed from to Cohen-Gibson syndrome, MIM# 617561",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:15:05.266980+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EED were set to ",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:14:34.795196+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EED was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:14:05.867742+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EED: Rating: GREEN; Mode of pathogenicity: None; Publications: 25787343, 27193220, 27868325, 28229514; Phenotypes: Cohen-Gibson syndrome, MIM# 617561; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EED",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:09:19.068001+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHD8 as ready",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:09:19.057744+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd8 has been classified as Green List (High Evidence).",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:09:16.818659+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHD8 were changed from to {Autism, susceptibility to, 18} 615032; CHD8-related neurodevelopmental syndrome",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:08:52.483350+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHD8 were set to ",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:08:13.319171+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CHD8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:07:43.415496+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CHD8: Rating: GREEN; Mode of pathogenicity: None; Publications: 31980904; Phenotypes: {Autism, susceptibility to, 18} 615032, CHD8-related neurodevelopmental syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CHD8",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:02:11.028070+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDKN1C as ready",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:02:11.017117+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdkn1c has been classified as Green List (High Evidence).",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:02:08.350578+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDKN1C were changed from to Beckwith-Wiedemann syndrome, MIM# 130650",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:01:37.654672+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDKN1C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2021-01-17T18:01:03.760115+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CDKN1C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Beckwith-Wiedemann syndrome, MIM# 130650; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:58:53.709840+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BRWD3 as ready",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:58:53.701670+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: brwd3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:58:51.042091+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BRWD3 were changed from to Mental retardation, X-linked 93, MIM# 300659",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:58:23.577098+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BRWD3 were set to ",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:57:44.601019+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BRWD3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:57:17.466575+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BRWD3 as Amber List (moderate evidence)",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:57:17.456467+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: brwd3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T17:56:46.889838+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BRWD3: Rating: AMBER; Mode of pathogenicity: None; Publications: 17668385; Phenotypes: Mental retardation, X-linked 93, MIM# 300659; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BRWD3",
"entity_type": "gene"
},
{
"created": "2021-01-17T13:53:15.975460+11:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.61",
"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": "2021-01-17T13:46:43.661774+11:00",
"panel_name": "Pancreatitis",
"panel_id": 154,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-01-17T13:45:09.268820+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-01-17T10:54:37.191827+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ18 as ready",
"entity_name": "KCNJ18",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:54:37.176670+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj18 has been classified as Red List (Low Evidence).",
"entity_name": "KCNJ18",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:53:59.245036+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ2 as ready",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:53:59.233690+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj2 has been classified as Green List (High Evidence).",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:53:56.577834+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCNJ2 were changed from Hypokalemic Periodic Paralysis, Type 2; Periodic paralysis; ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS; Episodic weakness; Andersen syndrome to Hypokalemic Periodic Paralysis, Type 2; Periodic paralysis; Andersen syndrome, MIM# 170390; Episodic weakness; Andersen syndrome",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:53:34.926776+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNJ2 were set to ",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:53:24.250870+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KCNJ2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11371347, 12796536; Phenotypes: Andersen syndrome, MIM# 170390; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:51:45.485190+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNA1 as ready",
"entity_name": "KCNA1",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:51:45.474457+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcna1 has been classified as Green List (High Evidence).",
"entity_name": "KCNA1",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:51:43.212593+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KCNA1 were set to ",
"entity_name": "KCNA1",
"entity_type": "gene"
},
{
"created": "2021-01-17T10:51:34.360985+11:00",
"panel_name": "Skeletal Muscle Channelopathies",
"panel_id": 302,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: KCNA1 was changed from to Other",
"entity_name": "KCNA1",
"entity_type": "gene"
}
]
}