{"count":221303,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=241","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=239","results":[{"created":"2025-04-30T15:56:12.083626+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.438","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCH1 were changed from Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, 128230 (3) to Dystonia, DOPA-responsive, with or without hyperphenylalaninaemia, MIM#128230","entity_name":"GCH1","entity_type":"gene"},{"created":"2025-04-30T15:55:53.171265+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.437","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCH1 were set to ","entity_name":"GCH1","entity_type":"gene"},{"created":"2025-04-30T15:55:20.812388+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.436","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCDH as ready","entity_name":"GCDH","entity_type":"gene"},{"created":"2025-04-30T15:55:20.806081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gcdh has been classified as Green List (High Evidence).","entity_name":"GCDH","entity_type":"gene"},{"created":"2025-04-30T15:55:18.140327+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.436","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCDH were changed from Glutaricaciduria, type I, 231670 (3) to Glutaric aciduria, type I, MIM#231670","entity_name":"GCDH","entity_type":"gene"},{"created":"2025-04-30T15:55:08.505526+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.435","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCDH were set to ","entity_name":"GCDH","entity_type":"gene"},{"created":"2025-04-30T15:54:45.392976+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.434","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GBE1 as ready","entity_name":"GBE1","entity_type":"gene"},{"created":"2025-04-30T15:54:45.386014+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.434","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gbe1 has been classified as Green List (High Evidence).","entity_name":"GBE1","entity_type":"gene"},{"created":"2025-04-30T15:54:43.016193+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.434","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GBE1 were changed from Glycogen storage disease IV, 232500 (3) to Glycogen storage disease IV, MIM#232500","entity_name":"GBE1","entity_type":"gene"},{"created":"2025-04-30T15:54:20.205255+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.433","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATM as ready","entity_name":"GATM","entity_type":"gene"},{"created":"2025-04-30T15:54:20.193955+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gatm has been classified as Green List (High Evidence).","entity_name":"GATM","entity_type":"gene"},{"created":"2025-04-30T15:54:17.900241+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.433","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATM were changed from Cerebral creatine deficiency syndrome 3, 612718 (3) to Cerebral creatine deficiency syndrome 3 MIM#612718; AGAT deficiency MONDO:0012996","entity_name":"GATM","entity_type":"gene"},{"created":"2025-04-30T15:54:07.011086+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.432","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GATM were set to ","entity_name":"GATM","entity_type":"gene"},{"created":"2025-04-30T15:53:43.001709+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.431","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GAMT as ready","entity_name":"GAMT","entity_type":"gene"},{"created":"2025-04-30T15:53:42.993921+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.431","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gamt has been classified as Green List (High Evidence).","entity_name":"GAMT","entity_type":"gene"},{"created":"2025-04-30T15:53:40.683526+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.431","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GAMT were changed from Cerebral creatine deficiency syndrome 2, 612736 (3) to Cerebral creatine deficiency syndrome 2 (MIM#612736)","entity_name":"GAMT","entity_type":"gene"},{"created":"2025-04-30T15:53:31.283934+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.430","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GAMT were set to ","entity_name":"GAMT","entity_type":"gene"},{"created":"2025-04-30T15:53:08.147768+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.429","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALT as ready","entity_name":"GALT","entity_type":"gene"},{"created":"2025-04-30T15:53:08.141564+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.429","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galt has been classified as Green List (High Evidence).","entity_name":"GALT","entity_type":"gene"},{"created":"2025-04-30T15:53:05.791344+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.429","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALT were changed from Galactosemia, 230400 (3) to Galactosaemia MIM# 230400","entity_name":"GALT","entity_type":"gene"},{"created":"2025-04-30T15:52:42.435887+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.428","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALNS as ready","entity_name":"GALNS","entity_type":"gene"},{"created":"2025-04-30T15:52:42.429427+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.428","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galns has been classified as Green List (High Evidence).","entity_name":"GALNS","entity_type":"gene"},{"created":"2025-04-30T15:52:40.277089+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.428","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALNS were changed from Mucopolysaccharidosis IVA, 253000 (3) to Mucopolysaccharidosis IVA, MIM#253000","entity_name":"GALNS","entity_type":"gene"},{"created":"2025-04-30T15:52:30.609792+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.427","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GALNS were set to ","entity_name":"GALNS","entity_type":"gene"},{"created":"2025-04-30T15:52:11.652083+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.426","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALC as ready","entity_name":"GALC","entity_type":"gene"},{"created":"2025-04-30T15:52:11.645606+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galc has been classified as Green List (High Evidence).","entity_name":"GALC","entity_type":"gene"},{"created":"2025-04-30T15:52:09.683144+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.426","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALC were changed from Krabbe disease, 245200 (3) to Krabbe disease, MIM# 245200; MONDO:0009499","entity_name":"GALC","entity_type":"gene"},{"created":"2025-04-30T15:52:00.147028+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.425","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GALC were set to ","entity_name":"GALC","entity_type":"gene"},{"created":"2025-04-30T15:51:39.570958+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.424","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GAA as ready","entity_name":"GAA","entity_type":"gene"},{"created":"2025-04-30T15:51:39.563736+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.424","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gaa has been classified as Green List (High Evidence).","entity_name":"GAA","entity_type":"gene"},{"created":"2025-04-30T15:51:37.115523+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.424","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GAA were changed from Glycogen storage disease II, 232300 (3) to Glycogen storage disease II, MIM#232300","entity_name":"GAA","entity_type":"gene"},{"created":"2025-04-30T15:51:27.588649+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.423","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GAA were set to ","entity_name":"GAA","entity_type":"gene"},{"created":"2025-04-30T15:51:04.755133+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.422","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: G6PC3 as ready","entity_name":"G6PC3","entity_type":"gene"},{"created":"2025-04-30T15:51:04.748632+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.422","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: g6pc3 has been classified as Green List (High Evidence).","entity_name":"G6PC3","entity_type":"gene"},{"created":"2025-04-30T15:51:01.280786+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.422","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: G6PC3 were changed from Dursun syndrome, 612541 (3) to Dursun syndrome, MIM# 612541; Neutropenia, severe congenital 4, autosomal recessive, MIM# 612541","entity_name":"G6PC3","entity_type":"gene"},{"created":"2025-04-30T15:50:40.413309+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.421","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: G6PC as ready","entity_name":"G6PC","entity_type":"gene"},{"created":"2025-04-30T15:50:40.406337+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.421","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: g6pc has been classified as Green List (High Evidence).","entity_name":"G6PC","entity_type":"gene"},{"created":"2025-04-30T15:50:38.260534+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.421","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: G6PC were changed from Glycogen storage disease Ia, 232200 (3) to Glycogen storage disease Ia (MIM# 232200)","entity_name":"G6PC","entity_type":"gene"},{"created":"2025-04-30T15:50:13.780629+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.420","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FUCA1 as ready","entity_name":"FUCA1","entity_type":"gene"},{"created":"2025-04-30T15:50:13.774562+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.420","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fuca1 has been classified as Green List (High Evidence).","entity_name":"FUCA1","entity_type":"gene"},{"created":"2025-04-30T15:50:11.345570+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.420","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FUCA1 were changed from Fucosidosis, 230000 (3) to Fucosidosis, MIM# 230000","entity_name":"FUCA1","entity_type":"gene"},{"created":"2025-04-30T15:49:50.466406+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.419","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FTSJ1 as ready","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2025-04-30T15:49:50.459410+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.419","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ftsj1 has been classified as Green List (High Evidence).","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2025-04-30T15:49:48.080793+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.419","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FTSJ1 were changed from Mental retardation, X-linked 9, 309549 (3) to Intellectual developmental disorder, X-linked 9 MIM#309549","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2025-04-30T15:49:33.278962+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.418","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FTSJ1 were set to ","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2025-04-30T15:49:10.586416+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.417","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FREM2 as ready","entity_name":"FREM2","entity_type":"gene"},{"created":"2025-04-30T15:49:10.579352+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.417","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frem2 has been classified as Green List (High Evidence).","entity_name":"FREM2","entity_type":"gene"},{"created":"2025-04-30T15:49:02.333658+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.417","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FREM2 were changed from Fraser syndrome, 219000 (3) to Fraser syndrome, MIM#219000","entity_name":"FREM2","entity_type":"gene"},{"created":"2025-04-30T15:48:49.566302+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.416","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FREM2 were set to ","entity_name":"FREM2","entity_type":"gene"},{"created":"2025-04-30T15:48:30.232933+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.415","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FRAS1 as ready","entity_name":"FRAS1","entity_type":"gene"},{"created":"2025-04-30T15:48:30.223083+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.415","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fras1 has been classified as Green List (High Evidence).","entity_name":"FRAS1","entity_type":"gene"},{"created":"2025-04-30T15:48:27.999064+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.415","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FRAS1 were changed from Fraser syndrome, 219000 (3) to Fraser syndrome 1 MIM#219000","entity_name":"FRAS1","entity_type":"gene"},{"created":"2025-04-30T15:48:17.137423+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.414","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FRAS1 were set to ","entity_name":"FRAS1","entity_type":"gene"},{"created":"2025-04-30T15:47:43.171806+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.413","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXRED1 as ready","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2025-04-30T15:47:43.165168+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.413","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxred1 has been classified as Green List (High Evidence).","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2025-04-30T15:47:40.444244+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.413","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXRED1 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 19, MIM# 618241","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2025-04-30T15:47:24.043532+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.412","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXRED1 were set to ","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2025-04-30T15:46:55.867417+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.411","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXN1 as ready","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-04-30T15:46:55.859244+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.411","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxn1 has been classified as Green List (High Evidence).","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-04-30T15:46:53.742883+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.411","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXN1 were changed from T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3) to T-cell immunodeficiency, congenital alopecia, and nail dystrophy MIM#601705","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-04-30T15:46:42.442166+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.410","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXN1 were set to ","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-04-30T15:46:06.484129+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.409","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FMR1 as ready","entity_name":"FMR1","entity_type":"gene"},{"created":"2025-04-30T15:46:06.477536+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.409","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fmr1 has been classified as Green List (High Evidence).","entity_name":"FMR1","entity_type":"gene"},{"created":"2025-04-30T15:45:57.875924+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.409","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FMR1 were changed from Fragile X syndrome to Fragile X syndrome, MIM #300624","entity_name":"FMR1","entity_type":"gene"},{"created":"2025-04-30T15:45:47.488298+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.408","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FMR1 were set to ","entity_name":"FMR1","entity_type":"gene"},{"created":"2025-04-30T15:43:25.665358+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.407","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLNA as ready","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-04-30T15:43:25.658909+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.407","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flna has been classified as Green List (High Evidence).","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-04-30T15:43:22.578054+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.407","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLNA were changed from FG syndrome 2, 300321 (3) to Frontometaphyseal dysplasia 1, MIM#305620; Heterotopia, periventricular, 1, MIM#300049; Intestinal pseudoobstruction, neuronal, MIM#300048; Melnick-Needles syndrome, MIM#309350; Otopalatodigital syndrome, type I, MIM#311300; Otopalatodigital syndrome, type II, MIM#304120; Terminal osseous dysplasia, MIM#300244","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-04-30T15:42:12.871731+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.406","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLNA were set to ","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-04-30T15:41:46.187557+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.405","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKTN as ready","entity_name":"FKTN","entity_type":"gene"},{"created":"2025-04-30T15:41:46.180706+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.405","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fktn has been classified as Green List (High Evidence).","entity_name":"FKTN","entity_type":"gene"},{"created":"2025-04-30T15:41:43.454203+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.405","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKTN were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4, 253800 (3) to Muscular dystrophy-dystroglycanopathy MONDO:0018276","entity_name":"FKTN","entity_type":"gene"},{"created":"2025-04-30T15:41:18.452114+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.404","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKTN were set to ","entity_name":"FKTN","entity_type":"gene"},{"created":"2025-04-30T15:40:48.308023+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.403","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKRP as ready","entity_name":"FKRP","entity_type":"gene"},{"created":"2025-04-30T15:40:48.298093+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.403","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkrp has been classified as Green List (High Evidence).","entity_name":"FKRP","entity_type":"gene"},{"created":"2025-04-30T15:40:37.341312+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.403","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKRP were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, 613153 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5 (MIM#613153); Muscular dystrophy-dystroglycanopathy (congenital with or without intellectual development), type B, 5 (MIM#606612); Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5 (MIM#607155)","entity_name":"FKRP","entity_type":"gene"},{"created":"2025-04-30T15:40:23.940704+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.402","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKRP were set to ","entity_name":"FKRP","entity_type":"gene"},{"created":"2025-04-30T15:40:08.464352+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.401","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKBP10 as ready","entity_name":"FKBP10","entity_type":"gene"},{"created":"2025-04-30T15:40:08.457336+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.401","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp10 has been classified as Green List (High Evidence).","entity_name":"FKBP10","entity_type":"gene"},{"created":"2025-04-30T15:40:05.861784+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.401","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKBP10 were changed from Bruck syndrome 1, 259450 (3) to Bruck syndrome 1, MIM#259450; osteogenesis imperfecta, type XI, MIM#610968","entity_name":"FKBP10","entity_type":"gene"},{"created":"2025-04-30T15:39:40.319693+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.400","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKBP10 were set to ","entity_name":"FKBP10","entity_type":"gene"},{"created":"2025-04-30T15:39:12.806582+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.399","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FHL1 as ready","entity_name":"FHL1","entity_type":"gene"},{"created":"2025-04-30T15:39:12.799095+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.399","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fhl1 has been classified as Green List (High Evidence).","entity_name":"FHL1","entity_type":"gene"},{"created":"2025-04-30T15:39:10.840501+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.399","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FHL1 were changed from Emery-Dreifuss muscular dystrophy 6, X-linked, 300696 (3) to Reducing body myopathy MONDO:0019948; X-linked Emery-Dreifuss muscular dystrophy MONDO:0010680","entity_name":"FHL1","entity_type":"gene"},{"created":"2025-04-30T15:38:59.950962+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.398","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FHL1 were set to ","entity_name":"FHL1","entity_type":"gene"},{"created":"2025-04-30T15:38:35.061708+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.397","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FH as ready","entity_name":"FH","entity_type":"gene"},{"created":"2025-04-30T15:38:35.054832+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.397","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fh has been classified as Green List (High Evidence).","entity_name":"FH","entity_type":"gene"},{"created":"2025-04-30T15:38:33.128979+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.397","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FH were changed from Fumarase deficiency, 606812 (3) to Fumarase deficiency, MIM# 606812","entity_name":"FH","entity_type":"gene"},{"created":"2025-04-30T15:38:22.680509+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.396","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FH were set to ","entity_name":"FH","entity_type":"gene"},{"created":"2025-04-30T15:37:57.874040+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.395","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FBXO7 as ready","entity_name":"FBXO7","entity_type":"gene"},{"created":"2025-04-30T15:37:57.865852+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.395","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbxo7 has been classified as Green List (High Evidence).","entity_name":"FBXO7","entity_type":"gene"},{"created":"2025-04-30T15:37:55.534352+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.395","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FBXO7 were changed from Parkinson disease 15, autosomal recessive, 260300 (3) to Parkinson disease 15, autosomal recessive, MIM#260300","entity_name":"FBXO7","entity_type":"gene"},{"created":"2025-04-30T15:37:44.210301+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.394","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FBXO7 were set to ","entity_name":"FBXO7","entity_type":"gene"},{"created":"2025-04-30T15:37:14.415921+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.393","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FBP1 as ready","entity_name":"FBP1","entity_type":"gene"},{"created":"2025-04-30T15:37:14.409392+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.393","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbp1 has been classified as Green List (High Evidence).","entity_name":"FBP1","entity_type":"gene"},{"created":"2025-04-30T15:37:11.726577+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.393","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FBP1 were changed from Fructose-1,6-bisphosphatase deficiency, 229700 (3) to Fructose-1,6-bisphosphatase deficiency, MIM#229700","entity_name":"FBP1","entity_type":"gene"},{"created":"2025-04-30T15:36:20.685056+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.392","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAT4 as ready","entity_name":"FAT4","entity_type":"gene"},{"created":"2025-04-30T15:36:20.675419+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.392","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fat4 has been classified as Green List (High Evidence).","entity_name":"FAT4","entity_type":"gene"},{"created":"2025-04-30T15:36:18.108177+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.392","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAT4 were changed from Hennekam lymphangiectasia-lymphedema syndrome 2, 616006 (3) to Hennekam lymphangiectasia-lymphedema syndrome 2 MIM#616006; Van Maldergem syndrome 2 MIM#615546","entity_name":"FAT4","entity_type":"gene"},{"created":"2025-04-30T15:36:09.027706+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.391","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAT4 were set to ","entity_name":"FAT4","entity_type":"gene"}]}