{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=220","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=218","results":[{"created":"2025-05-27T21:32:55.608856+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1073","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC52A3 were set to ","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2025-05-27T21:32:15.180752+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1072","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC52A2 as ready","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-05-27T21:32:15.173810+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1072","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc52a2 has been classified as Green List (High Evidence).","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-05-27T21:32:07.493898+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1072","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC52A2 were changed from Brown-Vialetto-Van Laere syndrome 2, 614707 (3) to Brown-Vialetto-Van Laere syndrome 2, MIM# 614707","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-05-27T21:31:17.497419+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1071","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC52A2 were set to ","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-05-27T21:30:45.180539+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1070","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC46A1 as ready","entity_name":"SLC46A1","entity_type":"gene"},{"created":"2025-05-27T21:30:45.160762+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1070","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc46a1 has been classified as Green List (High Evidence).","entity_name":"SLC46A1","entity_type":"gene"},{"created":"2025-05-27T21:30:32.203627+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1070","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC46A1 were changed from Folate malabsorption, hereditary, 229050 (3) to Folate malabsorption, hereditary, MIM# 229050","entity_name":"SLC46A1","entity_type":"gene"},{"created":"2025-05-27T21:30:15.240727+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1069","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC46A1 were set to ","entity_name":"SLC46A1","entity_type":"gene"},{"created":"2025-05-27T21:29:36.565472+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1068","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC45A2 as ready","entity_name":"SLC45A2","entity_type":"gene"},{"created":"2025-05-27T21:29:36.558330+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1068","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc45a2 has been classified as Green List (High Evidence).","entity_name":"SLC45A2","entity_type":"gene"},{"created":"2025-05-27T21:28:55.839345+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1068","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC45A2 were changed from Albinism, oculocutaneous, type IV, 606574 (3) to Albinism, oculocutaneous, type IV MIM#606574","entity_name":"SLC45A2","entity_type":"gene"},{"created":"2025-05-27T21:28:42.692590+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1067","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC45A2 were set to ","entity_name":"SLC45A2","entity_type":"gene"},{"created":"2025-05-27T21:23:25.192289+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1066","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC39A4 as ready","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2025-05-27T21:23:25.182976+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1066","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc39a4 has been classified as Green List (High Evidence).","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2025-05-27T21:23:19.364937+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1066","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC39A4 were changed from Acrodermatitis enteropathica, 201100 (3) to Acrodermatitis enteropathica, MIM# 201100","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2025-05-27T21:23:08.803709+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1065","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC39A4 were set to ","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2025-05-27T21:22:33.231734+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC38A8 as ready","entity_name":"SLC38A8","entity_type":"gene"},{"created":"2025-05-27T21:22:33.224777+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc38a8 has been classified as Green List (High Evidence).","entity_name":"SLC38A8","entity_type":"gene"},{"created":"2025-05-27T21:22:22.559481+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC38A8 were changed from Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3) to Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis (MIM#609218)","entity_name":"SLC38A8","entity_type":"gene"},{"created":"2025-05-27T21:22:04.959004+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1063","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC38A8 were set to ","entity_name":"SLC38A8","entity_type":"gene"},{"created":"2025-05-27T21:21:05.086355+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC37A4 as ready","entity_name":"SLC37A4","entity_type":"gene"},{"created":"2025-05-27T21:21:05.078090+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc37a4 has been classified as Green List (High Evidence).","entity_name":"SLC37A4","entity_type":"gene"},{"created":"2025-05-27T21:20:57.332381+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC37A4 were changed from Glycogen storage disease Ib, 232220 (3) to Glycogen storage disease Ib MIM#232220; Glycogen storage disease Ic MIM#232240; Glycogen Storage Disease I MONDO:0002413","entity_name":"SLC37A4","entity_type":"gene"},{"created":"2025-05-27T21:20:44.151247+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1061","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC37A4 were set to ","entity_name":"SLC37A4","entity_type":"gene"},{"created":"2025-05-27T21:19:07.940324+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC35A3 as ready","entity_name":"SLC35A3","entity_type":"gene"},{"created":"2025-05-27T21:19:07.933840+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc35a3 has been classified as Green List (High Evidence).","entity_name":"SLC35A3","entity_type":"gene"},{"created":"2025-05-27T21:18:50.765588+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC35A3 were changed from Arthrogryposis, mental retardation, and seizures (MIM615553) to Arthrogryposis, impaired intellectual development, and seizures MIM#615553","entity_name":"SLC35A3","entity_type":"gene"},{"created":"2025-05-27T21:18:00.754295+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1059","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A3 as ready","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-05-27T21:18:00.748010+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1059","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a3 has been classified as Green List (High Evidence).","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-05-27T21:17:44.698679+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1059","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC26A3 were set to ","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-05-27T21:16:51.505465+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A2 as ready","entity_name":"SLC26A2","entity_type":"gene"},{"created":"2025-05-27T21:16:51.499204+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a2 has been classified as Green List (High Evidence).","entity_name":"SLC26A2","entity_type":"gene"},{"created":"2025-05-27T21:16:40.608036+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC26A2 were changed from Achondrogenesis Ib, 600972 (3) to Achondrogenesis Ib MIM#600972; Atelosteogenesis, type II MIM#256050; De la Chapelle dysplasia MIM#256050; Diastrophic dysplasia MIM#222600; Diastrophic dysplasia, broad bone-platyspondylic variant MIM#222600; Epiphyseal dysplasia, multiple, 4 MIM#226900","entity_name":"SLC26A2","entity_type":"gene"},{"created":"2025-05-27T21:16:25.122169+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1057","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC26A2 were set to ","entity_name":"SLC26A2","entity_type":"gene"},{"created":"2025-05-27T21:15:55.531910+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A15 as ready","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2025-05-27T21:15:55.516257+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a15 has been classified as Green List (High Evidence).","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2025-05-27T21:15:50.474496+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A15 were changed from Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3) to Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome MIM#238970","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2025-05-27T21:15:36.068819+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1055","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A15 were set to ","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2025-05-27T21:14:17.429293+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A13 as ready","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-05-27T21:14:17.420359+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a13 has been classified as Green List (High Evidence).","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-05-27T21:14:00.291641+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A13 were changed from Citrullinemia, type II, neonatal-onset, 605814 (3) to Citrullinemia, type II, neonatal-onset, MIM#605814","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-05-27T21:13:36.984527+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1053","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A13 were set to ","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-05-27T21:13:12.970901+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A1 as ready","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-05-27T21:13:12.963546+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a1 has been classified as Green List (High Evidence).","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-05-27T21:13:08.674494+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A1 were changed from Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3) to Combined D-2- and L-2-hydroxyglutaric aciduria, MIM#615182; Myasthenic syndrome, congenital, 23, presynaptic, MIM#618197","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-05-27T21:12:44.431533+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1051","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A1 were set to ","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-05-27T21:12:19.715254+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1050","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC22A5 as ready","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2025-05-27T21:12:19.708444+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1050","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc22a5 has been classified as Green List (High Evidence).","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2025-05-27T21:12:15.458643+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1050","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC22A5 were changed from Carnitine deficiency, systemic primary, 212140 (3) to Carnitine deficiency, systemic primary, MIM# 212140, MONDO:0008919","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2025-05-27T21:12:04.440980+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC22A5 were set to ","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2025-05-27T20:28:16.844613+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1048","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC1A4 as ready","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2025-05-27T20:28:16.835216+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1048","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc1a4 has been classified as Green List (High Evidence).","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2025-05-27T20:28:11.039427+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1048","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC1A4 were changed from Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 (3) to Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2025-05-27T20:27:58.185790+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1047","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC1A4 were set to ","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2025-05-27T20:27:31.341495+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC19A3 as ready","entity_name":"SLC19A3","entity_type":"gene"},{"created":"2025-05-27T20:27:31.331696+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc19a3 has been classified as Green List (High Evidence).","entity_name":"SLC19A3","entity_type":"gene"},{"created":"2025-05-27T20:27:27.148962+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC19A3 were changed from Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 (3) to Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), MIM# 607483","entity_name":"SLC19A3","entity_type":"gene"},{"created":"2025-05-27T20:27:14.815211+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1045","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC19A3 were set to ","entity_name":"SLC19A3","entity_type":"gene"},{"created":"2025-05-27T20:26:36.758489+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC19A2 as ready","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2025-05-27T20:26:36.749896+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc19a2 has been classified as Green List (High Evidence).","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2025-05-27T20:26:33.107533+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC19A2 were changed from Thiamine-responsive megaloblastic anemia syndrome, 249270 (3) to Thiamine-responsive megaloblastic anemia syndrome, MIM#249270","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2025-05-27T20:26:22.114646+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1043","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC19A2 were set to ","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2025-05-27T20:25:31.212605+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1042","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC17A5 as ready","entity_name":"SLC17A5","entity_type":"gene"},{"created":"2025-05-27T20:25:31.204511+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1042","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc17a5 has been classified as Green List (High Evidence).","entity_name":"SLC17A5","entity_type":"gene"},{"created":"2025-05-27T20:25:27.307816+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1042","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC17A5 were changed from Sialic acid storage disorder, infantile, 269920 (3) to Sialic acid storage disorder, infantile (MIM#269920)","entity_name":"SLC17A5","entity_type":"gene"},{"created":"2025-05-27T20:25:16.516126+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1041","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC17A5 were set to ","entity_name":"SLC17A5","entity_type":"gene"},{"created":"2025-05-27T20:24:52.598720+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1040","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC16A2 as ready","entity_name":"SLC16A2","entity_type":"gene"},{"created":"2025-05-27T20:24:52.590917+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1040","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc16a2 has been classified as Green List (High Evidence).","entity_name":"SLC16A2","entity_type":"gene"},{"created":"2025-05-27T20:24:48.686831+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1040","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC16A2 were changed from Allan-Herndon-Dudley syndrome to Allan-Herndon-Dudley syndrome, MIM #300523","entity_name":"SLC16A2","entity_type":"gene"},{"created":"2025-05-27T20:24:37.295883+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1039","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC16A2 were set to ","entity_name":"SLC16A2","entity_type":"gene"},{"created":"2025-05-27T20:24:13.732031+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1038","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC12A1 as ready","entity_name":"SLC12A1","entity_type":"gene"},{"created":"2025-05-27T20:24:13.722492+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1038","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc12a1 has been classified as Green List (High Evidence).","entity_name":"SLC12A1","entity_type":"gene"},{"created":"2025-05-27T20:24:09.729993+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1038","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC12A1 were changed from Bartter syndrome, type 1, 601678 (3) to Bartter syndrome, type 1, MIM#601678","entity_name":"SLC12A1","entity_type":"gene"},{"created":"2025-05-27T20:23:55.728310+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1037","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC12A1 were set to ","entity_name":"SLC12A1","entity_type":"gene"},{"created":"2025-05-27T20:23:33.100031+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1036","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SKIV2L as ready","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-05-27T20:23:33.093524+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1036","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: skiv2l has been classified as Green List (High Evidence).","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-05-27T20:23:24.934906+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1036","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SKIV2L were changed from Trichohepatoenteric syndrome 2, 614602 (3) to Trichohepatoenteric syndrome 2, MIM# 614602","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-05-27T20:23:13.524529+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1035","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SKIV2L were set to ","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-05-27T20:16:26.903342+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1034","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SH3TC2 as ready","entity_name":"SH3TC2","entity_type":"gene"},{"created":"2025-05-27T20:16:26.896745+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1034","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sh3tc2 has been classified as Green List (High Evidence).","entity_name":"SH3TC2","entity_type":"gene"},{"created":"2025-05-27T20:16:16.913843+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1034","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SH3TC2 were changed from Charcot-Marie-Tooth disease, type 4C, 601596 (3) to Charcot-Marie-Tooth disease, type 4C MIM#601596","entity_name":"SH3TC2","entity_type":"gene"},{"created":"2025-05-27T20:15:36.244575+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGSH as ready","entity_name":"SGSH","entity_type":"gene"},{"created":"2025-05-27T20:15:36.235028+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgsh has been classified as Green List (High Evidence).","entity_name":"SGSH","entity_type":"gene"},{"created":"2025-05-27T20:15:22.107260+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGSH were changed from Mucopolysaccharidisis type IIIA (Sanfilippo A), 252900 (3) to Mucopolysaccharidosis type IIIA (Sanfilippo A), MIM# 252900; MONDO:0009655","entity_name":"SGSH","entity_type":"gene"},{"created":"2025-05-27T20:15:11.564296+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1032","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGSH were set to ","entity_name":"SGSH","entity_type":"gene"},{"created":"2025-05-27T20:14:45.745370+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCG as ready","entity_name":"SGCG","entity_type":"gene"},{"created":"2025-05-27T20:14:45.735886+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcg has been classified as Green List (High Evidence).","entity_name":"SGCG","entity_type":"gene"},{"created":"2025-05-27T20:14:41.340865+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCG were changed from Muscular dystrophy, limb-girdle, type 2C, 253700 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 5 MIM#253700","entity_name":"SGCG","entity_type":"gene"},{"created":"2025-05-27T20:14:12.283063+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1030","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCD as ready","entity_name":"SGCD","entity_type":"gene"},{"created":"2025-05-27T20:14:12.274316+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1030","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcd has been classified as Green List (High Evidence).","entity_name":"SGCD","entity_type":"gene"},{"created":"2025-05-27T20:14:06.210960+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1030","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCD were changed from Muscular dystrophy, limb-girdle, type 2F, 601287 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 6, MIM# 601287","entity_name":"SGCD","entity_type":"gene"},{"created":"2025-05-27T20:13:49.461553+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1029","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCD were set to ","entity_name":"SGCD","entity_type":"gene"},{"created":"2025-05-27T20:13:24.053021+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1028","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCB as ready","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-05-27T20:13:24.045245+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1028","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcb has been classified as Green List (High Evidence).","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-05-27T20:13:19.456451+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1028","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCB were changed from Muscular dystrophy, limb-girdle, type 2E, 604286 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 4 MIM#604286","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-05-27T20:12:53.229108+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1027","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCA as ready","entity_name":"SGCA","entity_type":"gene"},{"created":"2025-05-27T20:12:53.221904+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1027","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgca has been classified as Green List (High Evidence).","entity_name":"SGCA","entity_type":"gene"},{"created":"2025-05-27T20:12:49.081167+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1027","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCA were changed from Muscular dystrophy, limb-girdle, type 2D, 608099 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 3 MIM#608099; autosomal recessive limb-girdle muscular dystrophy type 2D, MONDO:0011968","entity_name":"SGCA","entity_type":"gene"},{"created":"2025-05-27T20:05:24.655494+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1026","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCA were set to ","entity_name":"SGCA","entity_type":"gene"}]}