{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1441","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1439","results":[{"created":"2021-01-17T21:49:54.525939+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":"Marked gene: HIST1H1E as ready","entity_name":"HIST1H1E","entity_type":"gene"},{"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"}]}