{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=245","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=243","results":[{"created":"2025-04-30T14:32:11.050817+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.246","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSD were changed from Ceroid lipofuscinosis, neuronal, 10, 610127 (3) to Ceroid lipofuscinosis, neuronal, 10, MIM# 610127","entity_name":"CTSD","entity_type":"gene"},{"created":"2025-04-30T14:31:42.496104+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.245","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSC as ready","entity_name":"CTSC","entity_type":"gene"},{"created":"2025-04-30T14:31:42.486215+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.245","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsc has been classified as Green List (High Evidence).","entity_name":"CTSC","entity_type":"gene"},{"created":"2025-04-30T14:31:40.294599+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.245","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSC were changed from Papillon-Lefevre syndrome, 245000 (3) to Haim-Munk syndrome MIM#245010; Papillon-Lefevre syndrome MIM#245000","entity_name":"CTSC","entity_type":"gene"},{"created":"2025-04-30T14:31:20.396765+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.244","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSA as ready","entity_name":"CTSA","entity_type":"gene"},{"created":"2025-04-30T14:31:20.386730+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.244","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsa has been classified as Green List (High Evidence).","entity_name":"CTSA","entity_type":"gene"},{"created":"2025-04-30T14:30:53.189629+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.244","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSA were changed from Galactosialidosis, 256540 (3) to Galactosialidosis MIM#256540","entity_name":"CTSA","entity_type":"gene"},{"created":"2025-04-30T14:30:44.851451+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.243","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTSA were set to ","entity_name":"CTSA","entity_type":"gene"},{"created":"2025-04-30T14:29:47.748347+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.242","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNS as ready","entity_name":"CTNS","entity_type":"gene"},{"created":"2025-04-30T14:29:47.740354+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.242","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctns has been classified as Green List (High Evidence).","entity_name":"CTNS","entity_type":"gene"},{"created":"2025-04-30T14:29:45.296412+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.242","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNS were changed from Cystinosis, nephropathic, 219800 (3) to Cystinosis, nephropathic MIM#219800","entity_name":"CTNS","entity_type":"gene"},{"created":"2025-04-30T14:29:34.928885+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.241","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNS were set to ","entity_name":"CTNS","entity_type":"gene"},{"created":"2025-04-30T14:28:59.022994+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.240","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CSPP1 as ready","entity_name":"CSPP1","entity_type":"gene"},{"created":"2025-04-30T14:28:59.015781+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.240","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cspp1 has been classified as Green List (High Evidence).","entity_name":"CSPP1","entity_type":"gene"},{"created":"2025-04-30T14:28:56.766504+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.240","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CSPP1 were changed from Joubert syndrome 21, 615636 (3) to Joubert syndrome 21 MIM#615636; MONDO:0014288","entity_name":"CSPP1","entity_type":"gene"},{"created":"2025-04-30T14:28:48.421621+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.239","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CSPP1 were set to ","entity_name":"CSPP1","entity_type":"gene"},{"created":"2025-04-30T14:28:26.440856+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.238","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRTAP as ready","entity_name":"CRTAP","entity_type":"gene"},{"created":"2025-04-30T14:28:26.433686+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.238","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crtap has been classified as Green List (High Evidence).","entity_name":"CRTAP","entity_type":"gene"},{"created":"2025-04-30T14:28:24.194303+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.238","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRTAP were changed from Osteogenesis imperfecta, type VII, 610682 (3) to Osteogenesis imperfecta, type VII MIM#610682","entity_name":"CRTAP","entity_type":"gene"},{"created":"2025-04-30T14:28:15.953277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.237","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRTAP were set to ","entity_name":"CRTAP","entity_type":"gene"},{"created":"2025-04-30T14:27:55.099688+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.236","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRB1 as ready","entity_name":"CRB1","entity_type":"gene"},{"created":"2025-04-30T14:27:55.090302+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.236","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crb1 has been classified as Green List (High Evidence).","entity_name":"CRB1","entity_type":"gene"},{"created":"2025-04-30T14:27:52.845460+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.236","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRB1 were changed from Leber congenital amaurosis 8, 613835 (3) to Leber congenital amaurosis 8, MIM#613835","entity_name":"CRB1","entity_type":"gene"},{"created":"2025-04-30T14:27:41.063586+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.235","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRB1 were set to ","entity_name":"CRB1","entity_type":"gene"},{"created":"2025-04-30T14:27:14.179905+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.234","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CPT2 as ready","entity_name":"CPT2","entity_type":"gene"},{"created":"2025-04-30T14:27:14.173497+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.234","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cpt2 has been classified as Green List (High Evidence).","entity_name":"CPT2","entity_type":"gene"},{"created":"2025-04-30T14:27:12.122438+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.234","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPT2 were changed from CPT II deficiency, lethal neonatal, 608836 (3) to CPT II deficiency, infantile MIM#600649; CPT II deficiency, lethal neonatal MIM#608836","entity_name":"CPT2","entity_type":"gene"},{"created":"2025-04-30T14:26:59.343875+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.233","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CPT2 were set to ","entity_name":"CPT2","entity_type":"gene"},{"created":"2025-04-30T14:26:40.514114+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.232","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CPT1A as ready","entity_name":"CPT1A","entity_type":"gene"},{"created":"2025-04-30T14:26:40.506950+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.232","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cpt1a has been classified as Green List (High Evidence).","entity_name":"CPT1A","entity_type":"gene"},{"created":"2025-04-30T14:26:11.996888+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.232","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPT1A were changed from CPT deficiency, hepatic, type IA, 255120 (3) to CPT deficiency, hepatic, type IA, MIM#255120","entity_name":"CPT1A","entity_type":"gene"},{"created":"2025-04-30T14:26:01.531872+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.231","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CPT1A were set to ","entity_name":"CPT1A","entity_type":"gene"},{"created":"2025-04-30T14:25:42.201687+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CPS1 as ready","entity_name":"CPS1","entity_type":"gene"},{"created":"2025-04-30T14:25:42.195347+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cps1 has been classified as Green List (High Evidence).","entity_name":"CPS1","entity_type":"gene"},{"created":"2025-04-30T14:25:39.881727+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPS1 were changed from Carbamoylphosphate synthetase I deficiency, 237300 (3) to Carbamoylphosphate synthetase I deficiency MIM#237300","entity_name":"CPS1","entity_type":"gene"},{"created":"2025-04-30T14:25:29.270797+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.229","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CPS1 were set to ","entity_name":"CPS1","entity_type":"gene"},{"created":"2025-04-30T14:24:45.632505+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COX15 as ready","entity_name":"COX15","entity_type":"gene"},{"created":"2025-04-30T14:24:45.624872+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cox15 has been classified as Green List (High Evidence).","entity_name":"COX15","entity_type":"gene"},{"created":"2025-04-30T14:24:43.018044+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COX15 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 (3) to Mitochondrial complex IV deficiency, nuclear type 6, MIM #615119","entity_name":"COX15","entity_type":"gene"},{"created":"2025-04-30T14:24:32.034059+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.227","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COX15 were set to ","entity_name":"COX15","entity_type":"gene"},{"created":"2025-04-30T14:24:13.880704+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COLQ as ready","entity_name":"COLQ","entity_type":"gene"},{"created":"2025-04-30T14:24:13.873862+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: colq has been classified as Green List (High Evidence).","entity_name":"COLQ","entity_type":"gene"},{"created":"2025-04-30T14:24:07.475498+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COLQ were changed from Myasthenic syndrome, congenital, 5, 603034 (3) to Myasthenic syndrome, congenital, 5 MIM#603034; MONDO:0011281","entity_name":"COLQ","entity_type":"gene"},{"created":"2025-04-30T14:23:57.397572+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.225","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COLQ were set to ","entity_name":"COLQ","entity_type":"gene"},{"created":"2025-04-30T14:23:39.233732+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COLEC11 as ready","entity_name":"COLEC11","entity_type":"gene"},{"created":"2025-04-30T14:23:39.226092+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: colec11 has been classified as Green List (High Evidence).","entity_name":"COLEC11","entity_type":"gene"},{"created":"2025-04-30T14:23:37.003198+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COLEC11 were changed from 3MC syndrome 2, 265050 (3) to 3MC syndrome 2, MIM# 265050; MONDO:0009927","entity_name":"COLEC11","entity_type":"gene"},{"created":"2025-04-30T14:23:27.591331+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.223","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COLEC11 were set to ","entity_name":"COLEC11","entity_type":"gene"},{"created":"2025-04-30T14:23:10.031360+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL7A1 as ready","entity_name":"COL7A1","entity_type":"gene"},{"created":"2025-04-30T14:23:10.024663+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col7a1 has been classified as Green List (High Evidence).","entity_name":"COL7A1","entity_type":"gene"},{"created":"2025-04-30T14:23:00.213876+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL7A1 were changed from Epidermolysis bullosa dystrophica, AR, 226600 (3) to Epidermolysis bullosa dystrophica inversa MIM#226600; Epidermolysis bullosa dystrophica, autosomal recessive MIM#226600; Epidermolysis bullosa dystrophica, localisata variant MIM#226600; Epidermolysis bullosa pruriginosa MIM#604129","entity_name":"COL7A1","entity_type":"gene"},{"created":"2025-04-30T14:22:29.466889+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.221","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL7A1 were set to ","entity_name":"COL7A1","entity_type":"gene"},{"created":"2025-04-30T14:22:10.737784+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL6A1 as ready","entity_name":"COL6A1","entity_type":"gene"},{"created":"2025-04-30T14:22:10.726971+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col6a1 has been classified as Green List (High Evidence).","entity_name":"COL6A1","entity_type":"gene"},{"created":"2025-04-30T14:22:07.749894+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL6A1 were changed from Ullrich congenital muscular dystrophy 1, 254090 (3) to Ullrich congenital muscular dystrophy 1A MIM#254090","entity_name":"COL6A1","entity_type":"gene"},{"created":"2025-04-30T14:21:57.585237+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.219","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL6A1 were set to ","entity_name":"COL6A1","entity_type":"gene"},{"created":"2025-04-30T14:21:15.112689+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL4A5 as ready","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-04-30T14:21:15.104831+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a5 has been classified as Green List (High Evidence).","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-04-30T14:21:12.649398+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL4A5 were changed from Alport syndrome 1, X-linked to Alport syndrome 1, X-linked, MIM#301050","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-04-30T14:20:59.074928+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.217","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL4A5 were set to ","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-04-30T14:20:41.338049+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL4A4 as ready","entity_name":"COL4A4","entity_type":"gene"},{"created":"2025-04-30T14:20:41.331004+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a4 has been classified as Green List (High Evidence).","entity_name":"COL4A4","entity_type":"gene"},{"created":"2025-04-30T14:20:36.493409+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL4A4 were changed from Alport syndrome, autosomal recessive, 203780 (3) to Alport syndrome 2, autosomal recessive MIM# 203780","entity_name":"COL4A4","entity_type":"gene"},{"created":"2025-04-30T14:20:26.107863+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.215","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL4A4 were set to ","entity_name":"COL4A4","entity_type":"gene"},{"created":"2025-04-30T14:20:10.555236+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL4A3 as ready","entity_name":"COL4A3","entity_type":"gene"},{"created":"2025-04-30T14:20:10.547796+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a3 has been classified as Green List (High Evidence).","entity_name":"COL4A3","entity_type":"gene"},{"created":"2025-04-30T14:20:08.224293+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL4A3 were changed from Alport syndrome, autosomal recessive, 203780 (3) to Alport syndrome 3b, autosomal recessive MIM#620536; MONDO:0957811","entity_name":"COL4A3","entity_type":"gene"},{"created":"2025-04-30T14:19:58.479966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.213","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL4A3 were set to ","entity_name":"COL4A3","entity_type":"gene"},{"created":"2025-04-30T14:19:39.710388+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL27A1 as ready","entity_name":"COL27A1","entity_type":"gene"},{"created":"2025-04-30T14:19:39.704203+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col27a1 has been classified as Green List (High Evidence).","entity_name":"COL27A1","entity_type":"gene"},{"created":"2025-04-30T14:19:36.725886+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL27A1 were changed from Steel Syndrome to Steel syndrome (MIM#615155)","entity_name":"COL27A1","entity_type":"gene"},{"created":"2025-04-30T14:19:26.915300+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.211","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL27A1 were set to ","entity_name":"COL27A1","entity_type":"gene"},{"created":"2025-04-30T14:19:10.609378+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL18A1 as ready","entity_name":"COL18A1","entity_type":"gene"},{"created":"2025-04-30T14:19:10.603135+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col18a1 has been classified as Green List (High Evidence).","entity_name":"COL18A1","entity_type":"gene"},{"created":"2025-04-30T14:19:08.601111+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL18A1 were changed from Knobloch syndrome, type 1, 267750 (3) to Knobloch syndrome, type 1 MIM#267750","entity_name":"COL18A1","entity_type":"gene"},{"created":"2025-04-30T14:18:58.138140+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.209","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL18A1 were set to ","entity_name":"COL18A1","entity_type":"gene"},{"created":"2025-04-30T14:18:37.301390+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.208","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL17A1 as ready","entity_name":"COL17A1","entity_type":"gene"},{"created":"2025-04-30T14:18:37.294678+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.208","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col17a1 has been classified as Green List (High Evidence).","entity_name":"COL17A1","entity_type":"gene"},{"created":"2025-04-30T14:18:35.504836+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.208","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL17A1 were changed from Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3) to Epidermolysis bullosa, junctional 4, intermediate, MIM# 619787","entity_name":"COL17A1","entity_type":"gene"},{"created":"2025-04-30T14:18:23.544536+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.207","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL17A1 were set to ","entity_name":"COL17A1","entity_type":"gene"},{"created":"2025-04-30T14:18:05.361472+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.206","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL11A2 as ready","entity_name":"COL11A2","entity_type":"gene"},{"created":"2025-04-30T14:18:05.354486+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.206","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col11a2 has been classified as Green List (High Evidence).","entity_name":"COL11A2","entity_type":"gene"},{"created":"2025-04-30T14:18:02.348712+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.206","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL11A2 were changed from Fibrochondrogenesis 2, 614524 (3) to Deafness, autosomal recessive 53 MIM#609706; Fibrochondrogenesis 2 MIM#614524; Otospondylomegaepiphyseal dysplasia, autosomal recessive MIM#215150","entity_name":"COL11A2","entity_type":"gene"},{"created":"2025-04-30T14:17:49.175019+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.205","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL11A2 were set to ","entity_name":"COL11A2","entity_type":"gene"},{"created":"2025-04-30T14:17:28.954150+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.204","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNGB3 as ready","entity_name":"CNGB3","entity_type":"gene"},{"created":"2025-04-30T14:17:28.942543+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.204","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cngb3 has been classified as Green List (High Evidence).","entity_name":"CNGB3","entity_type":"gene"},{"created":"2025-04-30T14:17:26.753593+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.204","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNGB3 were changed from Macular degeneration, juvenile, 248200 (3) to Achromatopsia 3 MIM#262300","entity_name":"CNGB3","entity_type":"gene"},{"created":"2025-04-30T14:17:19.237846+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.203","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNGB3 were set to ","entity_name":"CNGB3","entity_type":"gene"},{"created":"2025-04-30T14:16:53.329580+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.202","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLRN1 as ready","entity_name":"CLRN1","entity_type":"gene"},{"created":"2025-04-30T14:16:53.322725+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.202","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clrn1 has been classified as Green List (High Evidence).","entity_name":"CLRN1","entity_type":"gene"},{"created":"2025-04-30T14:16:51.560765+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.202","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLRN1 were changed from Usher syndrome, type 3A, 276902 (3) to Usher syndrome, type 3A, MIM#276902","entity_name":"CLRN1","entity_type":"gene"},{"created":"2025-04-30T14:16:42.405757+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.201","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLRN1 were set to ","entity_name":"CLRN1","entity_type":"gene"},{"created":"2025-04-30T14:16:23.766284+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.200","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLPB as ready","entity_name":"CLPB","entity_type":"gene"},{"created":"2025-04-30T14:16:23.759048+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.200","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clpb has been classified as Green List (High Evidence).","entity_name":"CLPB","entity_type":"gene"},{"created":"2025-04-30T14:16:21.194762+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.200","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 (3) to 3-methylglutaconic aciduria, type VIIB, autosomal recessive (MIM#616271)","entity_name":"CLPB","entity_type":"gene"},{"created":"2025-04-30T14:16:08.464705+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.199","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLPB were set to ","entity_name":"CLPB","entity_type":"gene"},{"created":"2025-04-30T14:15:54.189389+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.198","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLP1 as ready","entity_name":"CLP1","entity_type":"gene"},{"created":"2025-04-30T14:15:54.182378+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.198","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clp1 has been classified as Green List (High Evidence).","entity_name":"CLP1","entity_type":"gene"},{"created":"2025-04-30T14:15:52.406573+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.198","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLP1 were changed from Pontocerebellar hypoplasia, type 10, 615803 (3) to Pontocerebellar hypoplasia, type 10 MIM#615803","entity_name":"CLP1","entity_type":"gene"},{"created":"2025-04-30T14:15:42.220535+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.197","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLP1 were set to ","entity_name":"CLP1","entity_type":"gene"}]}