{"count":221303,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=240","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=238","results":[{"created":"2025-04-30T16:14:30.310840+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.484","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HAMP as ready","entity_name":"HAMP","entity_type":"gene"},{"created":"2025-04-30T16:14:30.303824+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hamp has been classified as Green List (High Evidence).","entity_name":"HAMP","entity_type":"gene"},{"created":"2025-04-30T16:14:27.820100+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.484","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAMP were changed from Hemochromatosis, type 2B, 613313 (3) to Haemochromatosis, type 2B MIM#613313","entity_name":"HAMP","entity_type":"gene"},{"created":"2025-04-30T16:14:15.949376+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.483","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HAMP were set to ","entity_name":"HAMP","entity_type":"gene"},{"created":"2025-04-30T16:13:55.086517+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.482","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HADHB as ready","entity_name":"HADHB","entity_type":"gene"},{"created":"2025-04-30T16:13:55.080277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.482","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hadhb has been classified as Green List (High Evidence).","entity_name":"HADHB","entity_type":"gene"},{"created":"2025-04-30T16:13:52.577131+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.482","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HADHB were changed from Trifunctional protein deficiency, 609015 (3) to Mitochondrial trifunctional protein deficiency 2 MIM#620300","entity_name":"HADHB","entity_type":"gene"},{"created":"2025-04-30T16:13:32.279943+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.481","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HADHA as ready","entity_name":"HADHA","entity_type":"gene"},{"created":"2025-04-30T16:13:32.272643+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.481","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hadha has been classified as Green List (High Evidence).","entity_name":"HADHA","entity_type":"gene"},{"created":"2025-04-30T16:13:30.144534+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.481","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HADHA were changed from Fatty liver, acute, of pregnancy, 609016 (3) to LCHAD deficiency MIM#609016; Mitochondrial trifunctional protein deficiency 1 MIM#609015","entity_name":"HADHA","entity_type":"gene"},{"created":"2025-04-30T16:13:11.617203+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.480","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HADH as ready","entity_name":"HADH","entity_type":"gene"},{"created":"2025-04-30T16:13:11.610407+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.480","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hadh has been classified as Green List (High Evidence).","entity_name":"HADH","entity_type":"gene"},{"created":"2025-04-30T16:13:09.491257+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.480","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HADH were changed from 3-hydroxyacyl-CoA dehydrogenase deficiency, 231530 (3) to 3-hydroxyacyl-CoA dehydrogenase deficiency MIM#231530","entity_name":"HADH","entity_type":"gene"},{"created":"2025-04-30T16:12:59.894067+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.479","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HADH were set to ","entity_name":"HADH","entity_type":"gene"},{"created":"2025-04-30T16:12:36.416171+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.478","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUSB as ready","entity_name":"GUSB","entity_type":"gene"},{"created":"2025-04-30T16:12:36.409058+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.478","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gusb has been classified as Green List (High Evidence).","entity_name":"GUSB","entity_type":"gene"},{"created":"2025-04-30T16:12:33.604661+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.478","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GUSB were changed from Mucopolysaccharidosis VII, 253220 (3) to Mucopolysaccharidosis VII, MIM# 253220","entity_name":"GUSB","entity_type":"gene"},{"created":"2025-04-30T16:12:23.976366+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.477","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GUSB were set to ","entity_name":"GUSB","entity_type":"gene"},{"created":"2025-04-30T16:11:42.344846+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.476","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUCY2D as ready","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2025-04-30T16:11:42.335971+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.476","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gucy2d has been classified as Green List (High Evidence).","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2025-04-30T16:11:40.006633+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.476","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GUCY2D were changed from Leber congenital amaurosis 1, 204000 (3) to Leber congenital amaurosis 1, MIM #204000","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2025-04-30T16:11:30.341604+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.475","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GUCY2D were set to ","entity_name":"GUCY2D","entity_type":"gene"},{"created":"2025-04-30T16:11:08.875343+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.474","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GSS as ready","entity_name":"GSS","entity_type":"gene"},{"created":"2025-04-30T16:11:08.867303+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.474","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gss has been classified as Green List (High Evidence).","entity_name":"GSS","entity_type":"gene"},{"created":"2025-04-30T16:11:06.535812+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.474","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GSS were changed from Glutathione synthetase deficiency, 266130 (3) to Glutathione synthetase deficiency MIM#266130","entity_name":"GSS","entity_type":"gene"},{"created":"2025-04-30T16:10:47.869326+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.473","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPSM2 as ready","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-04-30T16:10:47.860548+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.473","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpsm2 has been classified as Green List (High Evidence).","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-04-30T16:10:45.624357+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.473","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPSM2 were changed from Chudley-McCullough syndrome, 604213 (3) to Chudley-McCullough syndrome MIM#604213","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-04-30T16:10:32.315505+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.472","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPSM2 were set to ","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-04-30T16:09:58.944809+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPR143 as ready","entity_name":"GPR143","entity_type":"gene"},{"created":"2025-04-30T16:09:58.935552+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpr143 has been classified as Green List (High Evidence).","entity_name":"GPR143","entity_type":"gene"},{"created":"2025-04-30T16:09:49.316403+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPR143 were changed from Ocular albinism, type I, Nettleship-Falls type, 300500 (3) to Nystagmus 6, congenital, X-linked, MIM#300814; Ocular albinism, type I, Nettleship-Falls type, MIM#300500","entity_name":"GPR143","entity_type":"gene"},{"created":"2025-04-30T16:09:38.199937+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.470","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPR143 were set to ","entity_name":"GPR143","entity_type":"gene"},{"created":"2025-04-30T16:09:15.349992+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.469","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPC3 as ready","entity_name":"GPC3","entity_type":"gene"},{"created":"2025-04-30T16:09:15.338584+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.469","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":"2025-04-30T16:09:13.281369+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPC3 were changed from Simpson-Golabi-Behmel syndrome, type 1, 312870 (3) to Simpson-Golabi-Behmel syndrome, type 1, MIM #312870","entity_name":"GPC3","entity_type":"gene"},{"created":"2025-04-30T16:09:03.914772+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPC3 were set to ","entity_name":"GPC3","entity_type":"gene"},{"created":"2025-04-30T16:08:39.637249+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.467","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GORAB as ready","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-04-30T16:08:39.627726+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.467","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gorab has been classified as Green List (High Evidence).","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-04-30T16:08:36.280927+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.467","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GORAB were changed from Geroderma osteodysplasticum, 231070 (3) to Geroderma osteodysplasticum, MIM#231070; MONDO:0009271","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-04-30T16:08:26.127114+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.466","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GORAB were set to ","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-04-30T16:08:04.839661+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.465","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNS as ready","entity_name":"GNS","entity_type":"gene"},{"created":"2025-04-30T16:08:04.830140+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.465","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gns has been classified as Green List (High Evidence).","entity_name":"GNS","entity_type":"gene"},{"created":"2025-04-30T16:08:02.324539+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.465","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GNS were changed from Mucopolysaccharidosis type IIID, 252940 (3) to Mucopolysaccharidosis type IIID, MIM# 252940; Sanfilippo syndrome type D, MONDO:0009658","entity_name":"GNS","entity_type":"gene"},{"created":"2025-04-30T16:07:51.579886+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.464","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GNS were set to ","entity_name":"GNS","entity_type":"gene"},{"created":"2025-04-30T16:07:30.411934+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.463","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNPTG as ready","entity_name":"GNPTG","entity_type":"gene"},{"created":"2025-04-30T16:07:30.405151+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.463","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnptg has been classified as Green List (High Evidence).","entity_name":"GNPTG","entity_type":"gene"},{"created":"2025-04-30T16:07:00.101551+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.463","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GNPTG were changed from Mucolipidosis III gamma, 252605 (3) to Mucolipidosis III gamma, MIM# 252605","entity_name":"GNPTG","entity_type":"gene"},{"created":"2025-04-30T16:06:49.559772+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.462","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GNPTG were set to ","entity_name":"GNPTG","entity_type":"gene"},{"created":"2025-04-30T16:06:27.881346+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.461","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNPTAB as ready","entity_name":"GNPTAB","entity_type":"gene"},{"created":"2025-04-30T16:06:27.871161+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnptab has been classified as Green List (High Evidence).","entity_name":"GNPTAB","entity_type":"gene"},{"created":"2025-04-30T16:06:25.760033+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.461","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GNPTAB were changed from Mucolipidosis III alpha/beta, 252600 (3) to Mucolipidosis III alpha/beta MIM#252600; Mucolipidosis II alpha/beta MIM#252500","entity_name":"GNPTAB","entity_type":"gene"},{"created":"2025-04-30T16:06:07.083231+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.460","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNPAT as ready","entity_name":"GNPAT","entity_type":"gene"},{"created":"2025-04-30T16:06:07.075832+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.460","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnpat has been classified as Green List (High Evidence).","entity_name":"GNPAT","entity_type":"gene"},{"created":"2025-04-30T16:06:04.199668+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.460","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GNPAT were changed from Chondrodysplasia punctata, rhizomelic, type 2, 222765 (3) to Rhizomelic chondrodysplasia punctata, type 2 (MIM# 222765)","entity_name":"GNPAT","entity_type":"gene"},{"created":"2025-04-30T16:05:53.875303+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.459","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GNPAT were set to ","entity_name":"GNPAT","entity_type":"gene"},{"created":"2025-04-30T16:05:14.230473+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.458","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNB5 as ready","entity_name":"GNB5","entity_type":"gene"},{"created":"2025-04-30T16:05:14.219265+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.458","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnb5 has been classified as Green List (High Evidence).","entity_name":"GNB5","entity_type":"gene"},{"created":"2025-04-30T16:05:11.752726+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.458","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GNB5 were changed from Intellectual developmental disorder with cardiac arrhythmia, 617173 (3), Autosomal recessive to Lodder-Merla syndrome, type 1, with impaired intellectual development and cardiac arrhythmia (MIM#617173); Lodder-Merla syndrome, type 2, with developmental delay and with or without cardiac arrhythmia (MIM#617182)","entity_name":"GNB5","entity_type":"gene"},{"created":"2025-04-30T16:05:00.761143+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.457","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GNB5 were set to ","entity_name":"GNB5","entity_type":"gene"},{"created":"2025-04-30T16:04:38.356002+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.456","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLE1 as ready","entity_name":"GLE1","entity_type":"gene"},{"created":"2025-04-30T16:04:38.344267+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.456","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gle1 has been classified as Green List (High Evidence).","entity_name":"GLE1","entity_type":"gene"},{"created":"2025-04-30T16:04:36.232093+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.456","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLE1 were changed from Arthrogryposis, lethal, with anterior horn cell disease, 611890 (3) to Congenital arthrogryposis with anterior horn cell disease, MIM #611890; Lethal congenital contracture syndrome 1, MIM #253310","entity_name":"GLE1","entity_type":"gene"},{"created":"2025-04-30T16:04:23.860904+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.455","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLE1 were set to ","entity_name":"GLE1","entity_type":"gene"},{"created":"2025-04-30T16:04:03.439831+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.454","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLDC as ready","entity_name":"GLDC","entity_type":"gene"},{"created":"2025-04-30T16:04:03.427266+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.454","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gldc has been classified as Green List (High Evidence).","entity_name":"GLDC","entity_type":"gene"},{"created":"2025-04-30T16:04:01.370646+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.454","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLDC were changed from Glycine encephalopathy, 605899 (3) to Glycine encephalopathy1 (MIM#605899)","entity_name":"GLDC","entity_type":"gene"},{"created":"2025-04-30T16:03:47.170769+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.453","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLDC were set to ","entity_name":"GLDC","entity_type":"gene"},{"created":"2025-04-30T16:03:22.600560+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.452","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLB1 as ready","entity_name":"GLB1","entity_type":"gene"},{"created":"2025-04-30T16:03:22.593199+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.452","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glb1 has been classified as Green List (High Evidence).","entity_name":"GLB1","entity_type":"gene"},{"created":"2025-04-30T16:03:19.287147+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.452","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLB1 were changed from Mucopolysaccharidosis type IVB (Morquio), 253010 (3) to GM1-gangliosidosis, type I MIM#230500; GM1-gangliosidosis, type II MIM#230600; GM1-gangliosidosis, type III MIM#230650; Mucopolysaccharidosis type IVB (Morquio) MIM#253010","entity_name":"GLB1","entity_type":"gene"},{"created":"2025-04-30T16:03:08.020476+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.451","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLB1 were set to ","entity_name":"GLB1","entity_type":"gene"},{"created":"2025-04-30T16:02:16.542879+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.450","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLA as ready","entity_name":"GLA","entity_type":"gene"},{"created":"2025-04-30T16:02:16.536860+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.450","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gla has been classified as Green List (High Evidence).","entity_name":"GLA","entity_type":"gene"},{"created":"2025-04-30T16:02:12.878175+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.450","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLA were set to 29649853; 20301469","entity_name":"GLA","entity_type":"gene"},{"created":"2025-04-30T16:01:52.445795+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.449","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB1 as ready","entity_name":"GJB1","entity_type":"gene"},{"created":"2025-04-30T16:01:52.434109+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.449","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb1 has been classified as Green List (High Evidence).","entity_name":"GJB1","entity_type":"gene"},{"created":"2025-04-30T16:01:49.546959+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.449","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GJB1 were changed from Charcot-Marie-Tooth neuropathy, X-linked dominant, 1\t(MIM#302800) to Charcot-Marie-Tooth neuropathy, X-linked dominant, 1, MIM#302800","entity_name":"GJB1","entity_type":"gene"},{"created":"2025-04-30T16:01:38.327175+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.448","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GJB1 were set to ","entity_name":"GJB1","entity_type":"gene"},{"created":"2025-04-30T16:01:05.630125+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.447","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GHR as ready","entity_name":"GHR","entity_type":"gene"},{"created":"2025-04-30T16:01:05.623228+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.447","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ghr has been classified as Green List (High Evidence).","entity_name":"GHR","entity_type":"gene"},{"created":"2025-04-30T15:59:27.974018+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.447","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GHR were changed from Laron dwarfism, 262500 (3) to Laron dwarfism, MIM#262500","entity_name":"GHR","entity_type":"gene"},{"created":"2025-04-30T15:59:18.245833+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.446","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GHR were set to ","entity_name":"GHR","entity_type":"gene"},{"created":"2025-04-30T15:58:51.697877+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.445","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GFM1 as ready","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-04-30T15:58:51.691295+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.445","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gfm1 has been classified as Green List (High Evidence).","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-04-30T15:58:49.485809+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.445","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GFM1 were changed from Combined oxidative phosphorylation deficiency 1, 609060 (3) to Combined oxidative phosphorylation deficiency 1, MIM#609060","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-04-30T15:58:16.976302+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.444","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDF5 as ready","entity_name":"GDF5","entity_type":"gene"},{"created":"2025-04-30T15:58:16.969109+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.444","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdf5 has been classified as Green List (High Evidence).","entity_name":"GDF5","entity_type":"gene"},{"created":"2025-04-30T15:58:13.867585+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.444","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDF5 were changed from Chondrodysplasia, Grebe type, 200700 (3) to Acromesomelic dysplasia 2A MIM#200700; Acromesomelic dysplasia 2B MIM#228900","entity_name":"GDF5","entity_type":"gene"},{"created":"2025-04-30T15:57:59.914018+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.443","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDF5 were set to ","entity_name":"GDF5","entity_type":"gene"},{"created":"2025-04-30T15:57:26.442292+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.442","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDF1 as ready","entity_name":"GDF1","entity_type":"gene"},{"created":"2025-04-30T15:57:26.435482+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.442","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdf1 has been classified as Green List (High Evidence).","entity_name":"GDF1","entity_type":"gene"},{"created":"2025-04-30T15:57:23.933084+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.442","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDF1 were changed from Right atrial isomerism, 208530 (3) to Right atrial isomerism (Ivemark), MIM #208530","entity_name":"GDF1","entity_type":"gene"},{"created":"2025-04-30T15:57:13.520911+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.441","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDF1 were set to ","entity_name":"GDF1","entity_type":"gene"},{"created":"2025-04-30T15:56:55.579104+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.440","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDAP1 as ready","entity_name":"GDAP1","entity_type":"gene"},{"created":"2025-04-30T15:56:55.572415+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.440","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdap1 has been classified as Green List (High Evidence).","entity_name":"GDAP1","entity_type":"gene"},{"created":"2025-04-30T15:56:52.619362+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.440","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDAP1 were changed from Charcot-Marie-Tooth disease, recessive intermediate, A, 608340 (3) to Charcot-Marie-Tooth disease, axonal, type 2K, MIM #607831; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, MIM #607706; Charcot-Marie-Tooth disease, recessive intermediate, A, MIM #608340; Charcot-Marie-Tooth disease, type 4A, MIM#214400","entity_name":"GDAP1","entity_type":"gene"},{"created":"2025-04-30T15:56:41.874874+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.439","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDAP1 were set to ","entity_name":"GDAP1","entity_type":"gene"},{"created":"2025-04-30T15:56:15.398357+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.438","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCH1 as ready","entity_name":"GCH1","entity_type":"gene"},{"created":"2025-04-30T15:56:15.388924+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.438","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gch1 has been classified as Green List (High Evidence).","entity_name":"GCH1","entity_type":"gene"}]}