{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=223","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=221","results":[{"created":"2025-05-26T22:52:08.490316+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.928","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TTPA were set to ","entity_name":"TTPA","entity_type":"gene"},{"created":"2025-05-26T22:51:40.546980+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.927","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TULP1 as ready","entity_name":"TULP1","entity_type":"gene"},{"created":"2025-05-26T22:51:40.540262+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.927","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tulp1 has been classified as Green List (High Evidence).","entity_name":"TULP1","entity_type":"gene"},{"created":"2025-05-26T22:51:21.384032+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.927","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TULP1 were changed from Retinitis pigmentosa 14, 600132 (3) to Leber congenital amaurosis 15, MIM#613843; Retinitis pigmentosa 14, MIM#600132","entity_name":"TULP1","entity_type":"gene"},{"created":"2025-05-26T22:51:13.039920+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.926","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TULP1 were set to ","entity_name":"TULP1","entity_type":"gene"},{"created":"2025-05-26T22:50:52.852326+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.925","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TWNK as ready","entity_name":"TWNK","entity_type":"gene"},{"created":"2025-05-26T22:50:52.845707+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.925","user_name":"Seb Lunke","item_type":"entity","text":"Gene: twnk has been classified as Green List (High Evidence).","entity_name":"TWNK","entity_type":"gene"},{"created":"2025-05-26T22:50:34.707233+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.925","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TWNK were changed from Mitochondrial DNA depletion syndrome 7 (hepatocerebral type), 271245 (3) to Mitochondrial DNA depletion syndrome 7 (hepatocerebral type), MIM#271245; Perrault syndrome 5, MIM#616138","entity_name":"TWNK","entity_type":"gene"},{"created":"2025-05-26T22:50:17.890361+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.924","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TWNK were set to ","entity_name":"TWNK","entity_type":"gene"},{"created":"2025-05-26T22:49:11.445894+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.923","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TYMP as ready","entity_name":"TYMP","entity_type":"gene"},{"created":"2025-05-26T22:49:11.436427+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.923","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tymp has been classified as Green List (High Evidence).","entity_name":"TYMP","entity_type":"gene"},{"created":"2025-05-26T22:49:07.428599+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.923","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TYMP were changed from Mitochondrial DNA depletion syndrome 1 (MNGIE type), 603041 (3) to Mitochondrial DNA depletion syndrome 1 (MNGIE type), MIM#603041","entity_name":"TYMP","entity_type":"gene"},{"created":"2025-05-26T22:48:19.022362+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.922","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TYMP were set to ","entity_name":"TYMP","entity_type":"gene"},{"created":"2025-05-26T22:46:41.484429+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.921","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TYR as ready","entity_name":"TYR","entity_type":"gene"},{"created":"2025-05-26T22:46:41.477438+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.921","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tyr has been classified as Green List (High Evidence).","entity_name":"TYR","entity_type":"gene"},{"created":"2025-05-26T22:46:37.670335+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.921","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TYR were changed from Albinism, oculocutaneous, type IA, 203100 (3) to Oculocutaneous albinism type 1 (MONDO:0018135); Albinism, oculocutaneous, type IA, MIM#203100; Albinism, oculocutaneous, type IB, MIM#606952","entity_name":"TYR","entity_type":"gene"},{"created":"2025-05-26T22:46:04.202910+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.920","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TYR were set to ","entity_name":"TYR","entity_type":"gene"},{"created":"2025-05-25T23:18:24.721191+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.919","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TYRP1 as ready","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-05-25T23:18:24.714467+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.919","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tyrp1 has been classified as Green List (High Evidence).","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-05-25T23:18:19.573707+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.919","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TYRP1 were changed from Albinism, oculocutaneous, type III, 203290 (3) to Albinism, oculocutaneous, type III MIM#203290","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-05-25T23:18:09.013620+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.918","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TYRP1 were set to ","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-05-25T23:17:34.294266+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.917","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UBA5 as ready","entity_name":"UBA5","entity_type":"gene"},{"created":"2025-05-25T23:17:34.284865+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.917","user_name":"Seb Lunke","item_type":"entity","text":"Gene: uba5 has been classified as Green List (High Evidence).","entity_name":"UBA5","entity_type":"gene"},{"created":"2025-05-25T23:17:26.291696+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.917","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UBA5 were changed from Epileptic encephalopathy, early infantile, 44, 617132 (3), Autosomal recessive to Developmental and epileptic encephalopathy 44, MIM#617132","entity_name":"UBA5","entity_type":"gene"},{"created":"2025-05-25T23:17:16.230756+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.916","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UBA5 were set to ","entity_name":"UBA5","entity_type":"gene"},{"created":"2025-05-25T23:16:49.166205+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.915","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UBE2T as ready","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-05-25T23:16:49.159111+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.915","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ube2t has been classified as Green List (High Evidence).","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-05-25T23:16:46.000249+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.915","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UBE2T were changed from Fanconi anemia, complementation group T, 616435 (3) to Fanconi anemia, complementation group T MIM#616435","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-05-25T23:16:30.562817+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.914","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UBE2T were set to 32646888; 26119737; 26046368; 26085575","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-05-25T23:16:29.885125+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.913","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UBE2T were set to ","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-05-25T23:15:56.246748+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.912","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UBR1 as ready","entity_name":"UBR1","entity_type":"gene"},{"created":"2025-05-25T23:15:56.237024+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.912","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ubr1 has been classified as Green List (High Evidence).","entity_name":"UBR1","entity_type":"gene"},{"created":"2025-05-25T23:15:38.462722+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.912","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UBR1 were changed from Johanson-Blizzard syndrome, 243800 (3) to Johanson-Blizzard syndrome MIM#243800","entity_name":"UBR1","entity_type":"gene"},{"created":"2025-05-25T23:15:31.139157+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.911","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UBR1 were set to 24599544; 18553553; 16311597","entity_name":"UBR1","entity_type":"gene"},{"created":"2025-05-25T23:15:29.866622+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.910","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UBR1 were set to ","entity_name":"UBR1","entity_type":"gene"},{"created":"2025-05-25T23:14:39.177381+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.909","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UGT1A1 as ready","entity_name":"UGT1A1","entity_type":"gene"},{"created":"2025-05-25T23:14:39.170689+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.909","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ugt1a1 has been classified as Green List (High Evidence).","entity_name":"UGT1A1","entity_type":"gene"},{"created":"2025-05-25T23:14:33.614154+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.909","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UGT1A1 were changed from Crigler-Najjar syndrome, type I, 218800 (3) to Bilirubin UDP-glucuronosyltransferase 1 deficiency (Disorders of bile acid metabolism and transport); Crigler-Najjar syndrome, type I MIM#218800; Crigler-Najjar syndrome, type II MIM#606785","entity_name":"UGT1A1","entity_type":"gene"},{"created":"2025-05-25T23:14:20.069384+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.908","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UGT1A1 were set to ","entity_name":"UGT1A1","entity_type":"gene"},{"created":"2025-05-25T23:13:57.164631+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.907","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UNC13D as ready","entity_name":"UNC13D","entity_type":"gene"},{"created":"2025-05-25T23:13:57.158081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.907","user_name":"Seb Lunke","item_type":"entity","text":"Gene: unc13d has been classified as Green List (High Evidence).","entity_name":"UNC13D","entity_type":"gene"},{"created":"2025-05-25T23:13:49.784106+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.907","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UNC13D were changed from Hemophagocytic lymphohistiocytosis, familial, 3, 608898 (3) to Hemophagocytic lymphohistiocytosis, familial, 3, MIM#608898","entity_name":"UNC13D","entity_type":"gene"},{"created":"2025-05-25T23:13:24.955014+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.906","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UNC13D were set to ","entity_name":"UNC13D","entity_type":"gene"},{"created":"2025-05-25T23:12:52.689854+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.905","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: UPF3B as ready","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-05-25T23:12:52.683290+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.905","user_name":"Seb Lunke","item_type":"entity","text":"Gene: upf3b has been classified as Green List (High Evidence).","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-05-25T23:12:49.276284+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.905","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: UPF3B were changed from Mental retardation, X-linked, syndromic 14, 300676 (3) to Intellectual developmental disorder, X-linked syndromic 14 MIM#300676","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-05-25T23:12:42.850449+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.904","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: UPF3B were set to ","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-05-25T23:11:47.866164+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.903","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: USH1C as ready","entity_name":"USH1C","entity_type":"gene"},{"created":"2025-05-25T23:11:47.856357+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.903","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ush1c has been classified as Green List (High Evidence).","entity_name":"USH1C","entity_type":"gene"},{"created":"2025-05-25T23:11:42.761709+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.903","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: USH1C were changed from Usher syndrome, type 1C, 276904 (3) to Usher syndrome, type 1C MIM# 276904, MONDO:0010171","entity_name":"USH1C","entity_type":"gene"},{"created":"2025-05-25T23:11:29.977634+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.902","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: USH1C were set to ","entity_name":"USH1C","entity_type":"gene"},{"created":"2025-05-25T23:11:01.206254+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.901","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: USH1G as ready","entity_name":"USH1G","entity_type":"gene"},{"created":"2025-05-25T23:11:01.198485+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.901","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ush1g has been classified as Green List (High Evidence).","entity_name":"USH1G","entity_type":"gene"},{"created":"2025-05-25T23:10:57.254389+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.901","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: USH1G were changed from Usher syndrome, type 1G, 606943 (3) to Usher syndrome, type 1G MIM#606943","entity_name":"USH1G","entity_type":"gene"},{"created":"2025-05-25T23:10:47.198529+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.900","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: USH1G were set to ","entity_name":"USH1G","entity_type":"gene"},{"created":"2025-05-25T23:10:25.666237+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.899","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: USH2A as ready","entity_name":"USH2A","entity_type":"gene"},{"created":"2025-05-25T23:10:25.657028+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.899","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ush2a has been classified as Green List (High Evidence).","entity_name":"USH2A","entity_type":"gene"},{"created":"2025-05-25T23:09:55.629768+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.899","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: USH2A were changed from Usher syndrome, type 2A, 276901 (3) to Usher syndrome, type 2A, MIM#276901","entity_name":"USH2A","entity_type":"gene"},{"created":"2025-05-25T23:09:40.771235+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.898","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: USH2A were set to ","entity_name":"USH2A","entity_type":"gene"},{"created":"2025-05-25T23:09:02.350127+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.897","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: USP9X as ready","entity_name":"USP9X","entity_type":"gene"},{"created":"2025-05-25T23:09:02.342809+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.897","user_name":"Seb Lunke","item_type":"entity","text":"Gene: usp9x has been classified as Green List (High Evidence).","entity_name":"USP9X","entity_type":"gene"},{"created":"2025-05-25T23:08:48.269168+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.897","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: USP9X were changed from Intellectual developmental disorder 99 MIM#300919; syndromic, female-restricted Intellectual developmental disorder 99 MIM#300968 to Intellectual developmental disorder, X-linked 99, MIM#300919","entity_name":"USP9X","entity_type":"gene"},{"created":"2025-05-25T23:06:04.319574+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.896","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: USP9X were set to ","entity_name":"USP9X","entity_type":"gene"},{"created":"2025-05-25T23:05:51.761619+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.895","user_name":"Seb Lunke","item_type":"entity","text":"Mode of inheritance for gene: USP9X was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"USP9X","entity_type":"gene"},{"created":"2025-05-25T23:04:45.245194+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.894","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VLDLR as ready","entity_name":"VLDLR","entity_type":"gene"},{"created":"2025-05-25T23:04:45.233472+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.894","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vldlr has been classified as Green List (High Evidence).","entity_name":"VLDLR","entity_type":"gene"},{"created":"2025-05-25T23:04:23.042155+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.894","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VLDLR were changed from Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, 224050 (3) to Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1, MIM#224050","entity_name":"VLDLR","entity_type":"gene"},{"created":"2025-05-25T23:03:54.818901+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.893","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VLDLR were set to ","entity_name":"VLDLR","entity_type":"gene"},{"created":"2025-05-25T23:03:34.067272+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.892","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VPS11 were changed from Leukodystrophy, hypomyelinating, 12 (MIM#616683) to Leukodystrophy, hypomyelinating, 12 MIM#616683","entity_name":"VPS11","entity_type":"gene"},{"created":"2025-05-25T23:03:17.712102+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.891","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VPS11 as ready","entity_name":"VPS11","entity_type":"gene"},{"created":"2025-05-25T23:03:17.702765+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.891","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vps11 has been classified as Green List (High Evidence).","entity_name":"VPS11","entity_type":"gene"},{"created":"2025-05-25T23:03:12.196657+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.891","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VPS11 were changed from Leukodystrophy, hypomyelinating, 12, 616683 (3), Autosomal recessive to Leukodystrophy, hypomyelinating, 12 (MIM#616683)","entity_name":"VPS11","entity_type":"gene"},{"created":"2025-05-25T23:02:56.270024+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.890","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VPS11 were set to 27473128; 26307567; 27120463","entity_name":"VPS11","entity_type":"gene"},{"created":"2025-05-25T23:00:54.750318+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.889","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VPS53 as ready","entity_name":"VPS53","entity_type":"gene"},{"created":"2025-05-25T23:00:54.741186+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.889","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vps53 has been classified as Green List (High Evidence).","entity_name":"VPS53","entity_type":"gene"},{"created":"2025-05-25T23:00:26.970096+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.889","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VPS13B as ready","entity_name":"VPS13B","entity_type":"gene"},{"created":"2025-05-25T23:00:26.963395+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.889","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vps13b has been classified as Green List (High Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2025-05-25T23:00:19.299381+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.889","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VPS13B were changed from Cohen syndrome, 216550 (3) to Cohen syndrome, MIM# 216550","entity_name":"VPS13B","entity_type":"gene"},{"created":"2025-05-25T23:00:10.990826+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.888","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VPS13B were set to ","entity_name":"VPS13B","entity_type":"gene"},{"created":"2025-05-25T22:59:46.538899+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.887","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VPS45 as ready","entity_name":"VPS45","entity_type":"gene"},{"created":"2025-05-25T22:59:46.531929+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.887","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vps45 has been classified as Green List (High Evidence).","entity_name":"VPS45","entity_type":"gene"},{"created":"2025-05-25T22:59:38.492155+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.887","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VPS45 were changed from Neutropenia, severe congenital, 5, autosomal recessive, 615285 (3) to Neutropaenia, severe congenital, 5, autosomal recessive, MIM# 615285","entity_name":"VPS45","entity_type":"gene"},{"created":"2025-05-25T22:59:22.400409+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.886","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VPS45 were set to ","entity_name":"VPS45","entity_type":"gene"},{"created":"2025-05-25T22:59:03.314191+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.885","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VPS53 were changed from Pontocerebellar hypoplasia, type 2E, 615851 (3) to Pontocerebellar hypoplasia, type 2E, MIM#615851","entity_name":"VPS53","entity_type":"gene"},{"created":"2025-05-25T22:58:50.177613+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.884","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VPS53 were set to ","entity_name":"VPS53","entity_type":"gene"},{"created":"2025-05-25T22:57:04.696420+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.883","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VRK1 as ready","entity_name":"VRK1","entity_type":"gene"},{"created":"2025-05-25T22:57:04.689923+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.883","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vrk1 has been classified as Green List (High Evidence).","entity_name":"VRK1","entity_type":"gene"},{"created":"2025-05-25T22:56:58.427400+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.883","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VRK1 were changed from Pontocerebellar hypoplasia type 1A, 607596 (3) to Pontocerebellar hypoplasia type 1A, MIM# 607596, MONDO:0011866; Neuronopathy, distal hereditary motor, autosomal recessive 10, MIM# 620542","entity_name":"VRK1","entity_type":"gene"},{"created":"2025-05-25T22:56:47.173190+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.882","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VRK1 were set to ","entity_name":"VRK1","entity_type":"gene"},{"created":"2025-05-25T22:56:10.966085+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.881","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: VSX2 as ready","entity_name":"VSX2","entity_type":"gene"},{"created":"2025-05-25T22:56:10.955932+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.881","user_name":"Seb Lunke","item_type":"entity","text":"Gene: vsx2 has been classified as Green List (High Evidence).","entity_name":"VSX2","entity_type":"gene"},{"created":"2025-05-25T22:56:06.375041+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.881","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: VSX2 were changed from Microphthalmia with coloboma 3, 610092 (3) to Microphthalmia with coloboma 3, MIM# 610092; Microphthalmia, isolated 2, MIM# 610093","entity_name":"VSX2","entity_type":"gene"},{"created":"2025-05-25T22:55:51.354478+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.880","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: VSX2 were set to ","entity_name":"VSX2","entity_type":"gene"},{"created":"2025-05-25T22:55:18.458665+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.879","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: WAS as ready","entity_name":"WAS","entity_type":"gene"},{"created":"2025-05-25T22:55:18.451845+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.879","user_name":"Seb Lunke","item_type":"entity","text":"Gene: was has been classified as Green List (High Evidence).","entity_name":"WAS","entity_type":"gene"},{"created":"2025-05-25T22:55:01.956511+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.879","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: WAS were changed from Wiskott-Aldrich syndrome, 301000 (3) to Neutropenia, severe congenital, X-linked, MIM#300299; Thrombocytopenia, X-linked, MIM#313900; Wiskott-Aldrich syndrome, MIM#301000","entity_name":"WAS","entity_type":"gene"},{"created":"2025-05-25T22:54:54.107533+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.878","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: WAS were set to ","entity_name":"WAS","entity_type":"gene"},{"created":"2025-05-25T22:54:02.220311+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.877","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: WDR34 as ready","entity_name":"WDR34","entity_type":"gene"},{"created":"2025-05-25T22:54:02.213675+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.877","user_name":"Seb Lunke","item_type":"entity","text":"Gene: wdr34 has been classified as Green List (High Evidence).","entity_name":"WDR34","entity_type":"gene"},{"created":"2025-05-25T22:53:57.483417+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.877","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: WDR34 were changed from Short-rib thoracic dysplasia 11 with or without polydactyly, 615633 (3) to Short-rib thoracic dysplasia 11 with or without polydactyly MIM# 615633, MONDO:0014287","entity_name":"WDR34","entity_type":"gene"}]}