{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=246","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=244","results":[{"created":"2025-04-30T14:15:04.676153+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.196","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLN8 as ready","entity_name":"CLN8","entity_type":"gene"},{"created":"2025-04-30T14:15:04.666758+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.196","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cln8 has been classified as Green List (High Evidence).","entity_name":"CLN8","entity_type":"gene"},{"created":"2025-04-30T14:15:02.245524+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.196","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLN8 were changed from Ceroid lipofuscinosis, neuronal, 8, 600143 (3) to Ceroid lipofuscinosis, neuronal, 8, MIM# 600143","entity_name":"CLN8","entity_type":"gene"},{"created":"2025-04-30T14:14:32.415448+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.195","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLN6 as ready","entity_name":"CLN6","entity_type":"gene"},{"created":"2025-04-30T14:14:32.405966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.195","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cln6 has been classified as Green List (High Evidence).","entity_name":"CLN6","entity_type":"gene"},{"created":"2025-04-30T14:14:30.640194+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.195","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLN6 were changed from Ceroid lipofuscinosis, neuronal 6, 601780 (3) to Ceroid lipofuscinosis, neuronal 6, MIM#601780","entity_name":"CLN6","entity_type":"gene"},{"created":"2025-04-30T14:14:21.102843+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.194","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLN6 were set to ","entity_name":"CLN6","entity_type":"gene"},{"created":"2025-04-30T14:14:05.586479+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLN5 as ready","entity_name":"CLN5","entity_type":"gene"},{"created":"2025-04-30T14:14:05.580373+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cln5 has been classified as Green List (High Evidence).","entity_name":"CLN5","entity_type":"gene"},{"created":"2025-04-30T14:14:00.261345+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.193","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLN5 were changed from Ceroid lipofuscinosis, neuronal, 5, 256731 (3) to Ceroid lipofuscinosis, neuronal, 5, MIM# 256731; MONDO:0009745","entity_name":"CLN5","entity_type":"gene"},{"created":"2025-04-30T14:13:42.388906+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.192","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLCN7 as ready","entity_name":"CLCN7","entity_type":"gene"},{"created":"2025-04-30T14:13:42.381186+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.192","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn7 has been classified as Green List (High Evidence).","entity_name":"CLCN7","entity_type":"gene"},{"created":"2025-04-30T14:13:39.125008+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.192","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLCN7 were changed from Osteopetrosis, autosomal recessive 4, 611490 (3) to Osteopetrosis, autosomal recessive 4, MIM#611490","entity_name":"CLCN7","entity_type":"gene"},{"created":"2025-04-30T14:13:28.931956+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.191","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLCN7 were set to ","entity_name":"CLCN7","entity_type":"gene"},{"created":"2025-04-30T14:13:12.798802+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.190","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLCN5 as ready","entity_name":"CLCN5","entity_type":"gene"},{"created":"2025-04-30T14:13:12.789376+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn5 has been classified as Green List (High Evidence).","entity_name":"CLCN5","entity_type":"gene"},{"created":"2025-04-30T14:13:10.337186+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.190","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLCN5 were changed from Dent disease, 300009 (3) to Dent disease, MIM#300009","entity_name":"CLCN5","entity_type":"gene"},{"created":"2025-04-30T14:12:50.814363+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.189","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CKAP2L as ready","entity_name":"CKAP2L","entity_type":"gene"},{"created":"2025-04-30T14:12:50.807497+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.189","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ckap2l has been classified as Green List (High Evidence).","entity_name":"CKAP2L","entity_type":"gene"},{"created":"2025-04-30T14:12:48.025190+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CKAP2L were changed from Filippi syndrome, 272440 (3) to Filippi syndrome MIM#272440","entity_name":"CKAP2L","entity_type":"gene"},{"created":"2025-04-30T14:12:38.248185+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.188","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CKAP2L were set to ","entity_name":"CKAP2L","entity_type":"gene"},{"created":"2025-04-30T14:12:19.346323+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.187","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CIITA as ready","entity_name":"CIITA","entity_type":"gene"},{"created":"2025-04-30T14:12:19.339970+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.187","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ciita has been classified as Green List (High Evidence).","entity_name":"CIITA","entity_type":"gene"},{"created":"2025-04-30T14:12:16.858544+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.187","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CIITA were changed from Bare lymphocyte syndrome, type II, complementation group A, 209920 (3) to MHC class II deficiency 1 MIM#209920","entity_name":"CIITA","entity_type":"gene"},{"created":"2025-04-30T14:11:54.444626+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.186","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CIITA were set to ","entity_name":"CIITA","entity_type":"gene"},{"created":"2025-04-30T14:11:09.951367+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.185","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHRNG as ready","entity_name":"CHRNG","entity_type":"gene"},{"created":"2025-04-30T14:11:09.943922+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.185","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chrng has been classified as Green List (High Evidence).","entity_name":"CHRNG","entity_type":"gene"},{"created":"2025-04-30T14:11:08.047996+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.185","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHRNG were changed from Escobar syndrome, 265000 (3) to Escobar syndrome (MIM# 265000); Multiple pterygium syndrome, lethal type, (MIM# 253290)","entity_name":"CHRNG","entity_type":"gene"},{"created":"2025-04-30T14:10:47.251698+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.184","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHRNG were set to ","entity_name":"CHRNG","entity_type":"gene"},{"created":"2025-04-30T14:10:28.934491+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.183","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHRNE as ready","entity_name":"CHRNE","entity_type":"gene"},{"created":"2025-04-30T14:10:28.924138+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.183","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chrne has been classified as Green List (High Evidence).","entity_name":"CHRNE","entity_type":"gene"},{"created":"2025-04-30T14:10:26.578373+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.183","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHRNE were changed from Myasthenic syndrome, congenital, 4A, slow-channel, 605809 (3) to Myasthenic syndrome, congenital, 4A, slow-channel MIM#605809; Myasthenic syndrome, congenital, 4B, fast-channel MIM#616324; Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency MIM#608931","entity_name":"CHRNE","entity_type":"gene"},{"created":"2025-04-30T14:10:16.131068+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.182","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHRNE were set to ","entity_name":"CHRNE","entity_type":"gene"},{"created":"2025-04-30T14:09:43.942087+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHAT as ready","entity_name":"CHAT","entity_type":"gene"},{"created":"2025-04-30T14:09:43.935285+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chat has been classified as Green List (High Evidence).","entity_name":"CHAT","entity_type":"gene"},{"created":"2025-04-30T14:09:31.907140+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.181","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHAT were changed from Myasthenic syndrome, congenital, 6, presynaptic, 254210 (3) to Myasthenic syndrome, congenital, 6, presynaptic MIM#254210","entity_name":"CHAT","entity_type":"gene"},{"created":"2025-04-30T14:08:38.933770+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.180","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHAT were set to ","entity_name":"CHAT","entity_type":"gene"},{"created":"2025-04-30T14:08:11.481795+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.179","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CFTR as ready","entity_name":"CFTR","entity_type":"gene"},{"created":"2025-04-30T14:08:11.470781+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cftr has been classified as Green List (High Evidence).","entity_name":"CFTR","entity_type":"gene"},{"created":"2025-04-30T14:08:09.337035+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.179","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CFTR were changed from Cystic fibrosis, 219700 (3) to Cystic fibrosis, MIM#219700; MONDO:0009061","entity_name":"CFTR","entity_type":"gene"},{"created":"2025-04-30T14:08:00.573790+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.178","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CFTR were set to ","entity_name":"CFTR","entity_type":"gene"},{"created":"2025-04-30T14:07:41.696139+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.177","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP41 as ready","entity_name":"CEP41","entity_type":"gene"},{"created":"2025-04-30T14:07:41.689637+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.177","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep41 has been classified as Green List (High Evidence).","entity_name":"CEP41","entity_type":"gene"},{"created":"2025-04-30T14:07:39.462963+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.177","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP41 were changed from Joubert syndrome 15, 614464 (3) to Joubert syndrome 15, MIM# 614464","entity_name":"CEP41","entity_type":"gene"},{"created":"2025-04-30T14:07:29.413813+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.176","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP41 were set to ","entity_name":"CEP41","entity_type":"gene"},{"created":"2025-04-30T14:07:13.091064+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.175","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP290 as ready","entity_name":"CEP290","entity_type":"gene"},{"created":"2025-04-30T14:07:13.083204+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep290 has been classified as Green List (High Evidence).","entity_name":"CEP290","entity_type":"gene"},{"created":"2025-04-30T14:07:10.496166+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.175","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP290 were changed from Joubert syndrome 5, 610188 (3) to CEP290-related ciliopathy MONDO:0100451; Bardet-Biedl syndrome 14, MIM# 615991; Joubert syndrome 5 610188; Leber congenital amaurosis 10, MIM# 611755; Meckel syndrome 4, MIM# 611134; Senior-Loken syndrome 6, MIM# 610189","entity_name":"CEP290","entity_type":"gene"},{"created":"2025-04-30T14:07:00.852754+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.174","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP290 were set to ","entity_name":"CEP290","entity_type":"gene"},{"created":"2025-04-30T14:06:33.811777+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.173","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP152 as ready","entity_name":"CEP152","entity_type":"gene"},{"created":"2025-04-30T14:06:33.805526+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep152 has been classified as Green List (High Evidence).","entity_name":"CEP152","entity_type":"gene"},{"created":"2025-04-30T14:06:31.185498+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.173","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP152 were changed from Seckel syndrome 5, 613823 (3) to Microcephaly 9, primary, autosomal recessive, MIM# 614852; MONDO:0013923; Seckel syndrome 5, MIM# 613823; MONDO:0013443","entity_name":"CEP152","entity_type":"gene"},{"created":"2025-04-30T14:06:22.459285+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.172","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP152 were set to ","entity_name":"CEP152","entity_type":"gene"},{"created":"2025-04-30T14:06:03.210942+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.171","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CENPJ as ready","entity_name":"CENPJ","entity_type":"gene"},{"created":"2025-04-30T14:06:03.200480+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cenpj has been classified as Green List (High Evidence).","entity_name":"CENPJ","entity_type":"gene"},{"created":"2025-04-30T14:06:00.602512+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.171","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CENPJ were changed from Microcephaly 6, primary, autosomal recessive, 608393 (3) to Microcephaly 6, primary MIM#608393; Seckel syndrome 4 MIM#613676","entity_name":"CENPJ","entity_type":"gene"},{"created":"2025-04-30T14:05:51.144644+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.170","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CENPJ were set to ","entity_name":"CENPJ","entity_type":"gene"},{"created":"2025-04-30T14:05:26.636918+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.169","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDH23 as ready","entity_name":"CDH23","entity_type":"gene"},{"created":"2025-04-30T14:05:26.630807+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.169","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdh23 has been classified as Green List (High Evidence).","entity_name":"CDH23","entity_type":"gene"},{"created":"2025-04-30T14:05:22.035455+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.169","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDH23 were changed from Usher syndrome, type 1D, 601067 (3) to Usher syndrome, type 1D (MIM#601067)","entity_name":"CDH23","entity_type":"gene"},{"created":"2025-04-30T14:05:11.419752+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.168","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CDH23 were set to ","entity_name":"CDH23","entity_type":"gene"},{"created":"2025-04-30T14:04:55.469722+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.167","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD40LG as ready","entity_name":"CD40LG","entity_type":"gene"},{"created":"2025-04-30T14:04:55.462498+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.167","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd40lg has been classified as Green List (High Evidence).","entity_name":"CD40LG","entity_type":"gene"},{"created":"2025-04-30T14:04:53.255260+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.167","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD40LG were changed from Immunodeficiency, X-linked, with hyper-IgM, 308230 (3) to Immunodeficiency, X-linked, with hyper-IgM MIM# 308230","entity_name":"CD40LG","entity_type":"gene"},{"created":"2025-04-30T14:04:44.021343+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.166","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD40LG were set to ","entity_name":"CD40LG","entity_type":"gene"},{"created":"2025-04-30T11:56:31.525249+10:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.56","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: IFT57 as ready","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:56:31.518836+10:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.56","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:56:05.969038+10:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.56","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: IFT57 as Amber List (moderate evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:56:05.958517+10:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.56","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:49.492422+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.283","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: IFT57 as Amber List (moderate evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:49.483046+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.283","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:15.936594+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"1.68","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: IFT57 as Amber List (moderate evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:15.930340+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"1.68","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:08.398124+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"1.67","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: IFT57 as ready","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:54:08.386172+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"1.67","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Red List (Low Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:46.411325+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.12","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: IFT57 as ready","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:46.404872+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.12","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:42.790077+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.12","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: IFT57 as Amber List (moderate evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:42.784093+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.12","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:10.709453+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2519","user_name":"Krithika Murali","item_type":"entity","text":"Phenotypes for gene: IFT57 were changed from Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308 to Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:53:06.857643+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2518","user_name":"Krithika Murali","item_type":"entity","text":"Phenotypes for gene: IFT57 were changed from Orofaciodigital syndrome XVIII, MIM# 617927 to Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:52:50.109385+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2517","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: IFT57 as Amber List (moderate evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:52:50.102451+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2517","user_name":"Krithika Murali","item_type":"entity","text":"Gene: ift57 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2025-04-30T11:51:36.992496+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.120","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: UGGT1 as Green List (high evidence)","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:51:36.980212+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.120","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Green List (High Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:51:28.716151+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.119","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: UGGT1 as ready","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:51:28.708655+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.119","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Red List (Low Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:50:50.478749+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.146","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: UGGT1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID:40267907; Phenotypes: Congenital disorder of glycosylation - MONDO:0015286, UGGT1-CDG; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:50:13.596350+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.146","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: UGGT1 as Green List (high evidence)","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:50:13.585677+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.146","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Green List (High Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:24.860870+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: UGGT1 as Amber List (moderate evidence)","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:24.855040+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Amber List (Moderate Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:12.123166+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: UGGT1 as ready","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:12.115103+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Amber List (Moderate Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:11.213881+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: UGGT1 as Amber List (moderate evidence)","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:49:11.202645+10:00","panel_name":"Renal Macrocystic Disease","panel_id":194,"panel_version":"0.85","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Amber List (Moderate Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:48:18.921206+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.305","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: UGGT1 as Green List (high evidence)","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:48:18.911826+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.305","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Green List (High Evidence).","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:48:12.133750+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.304","user_name":"Krithika Murali","item_type":"entity","text":"Marked gene: UGGT1 as ready","entity_name":"UGGT1","entity_type":"gene"},{"created":"2025-04-30T11:48:12.121823+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.304","user_name":"Krithika Murali","item_type":"entity","text":"Gene: uggt1 has been classified as Red List (Low Evidence).","entity_name":"UGGT1","entity_type":"gene"}]}