{"count":220613,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=114","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=112","results":[{"created":"2025-11-26T15:46:07.928801+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"1.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:43:55.042407+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.445","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COQ5 were changed from Coenzyme Q10 deficiency, primary 9, MIM#619028; Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability to Coenzyme Q10 deficiency, primary, 9 MIM#619028","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:42:59.493917+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.444","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COQ5 were set to 29044765","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:42:27.601875+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.443","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ5 as Green List (high evidence)","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:42:27.591463+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.443","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:41:28.087133+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.286","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COQ5 as ready","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:41:28.078383+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.286","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:41:00.632736+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1090","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COQ5 were changed from Coenzyme Q10 deficiency, primary 9, MIM#619028; Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability to Coenzyme Q10 deficiency, primary, 9 MIM#619028","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:40:20.258499+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1089","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COQ5 were set to 29044765","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:39:43.420737+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1088","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ5 as Green List (high evidence)","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:39:43.411650+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1088","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:39:36.517838+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.286","user_name":"Zornitza Stark","item_type":"panel","text":"Copied gene COQ5 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-26T15:39:35.847524+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.286","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COQ5 was added\ngene: COQ5 was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list,Victorian Clinical Genetics Services\nMode of inheritance for gene: COQ5 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COQ5 were set to 29044765; 37599337; 21937992; 41199775; 36266294\nPhenotypes for gene: COQ5 were set to Coenzyme Q10 deficiency, primary 9, MIM#619028","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:39:24.236793+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1088","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ5 as Green List (high evidence)","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:39:24.221780+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1088","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:37:55.815203+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"1.66","user_name":"Zornitza Stark","item_type":"panel","text":"Added reviews for gene COQ5 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-26T15:34:46.585487+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3663","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ5 as Green List (high evidence)","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T15:34:46.577934+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq5 has been classified as Green List (High Evidence).","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T14:35:30.311583+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1087","user_name":"Lucy Spencer","item_type":"panel","text":"Added reviews for gene COQ5 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-26T14:34:32.366560+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.442","user_name":"Lucy Spencer","item_type":"panel","text":"Added reviews for gene COQ5 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-26T14:33:48.126996+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"1.65","user_name":"Lucy Spencer","item_type":"panel","text":"Added reviews for gene COQ5 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-26T14:32:11.590860+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3662","user_name":"Lucy Spencer","item_type":"entity","text":"Phenotypes for gene: COQ5 were changed from Coenzyme Q10 deficiency, primary 9, MIM#619028; Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability to Coenzyme Q10 deficiency, primary 9, MIM#619028","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T14:31:56.816612+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3661","user_name":"Lucy Spencer","item_type":"entity","text":"Publications for gene: COQ5 were set to 29044765","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T14:31:18.353709+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3660","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: COQ5: Rating: GREEN; Mode of pathogenicity: None; Publications: 29044765, 37599337, 21937992, 41199775, 36266294; Phenotypes: Coenzyme Q10 deficiency, primary, 9 MIM#619028; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COQ5","entity_type":"gene"},{"created":"2025-11-26T14:02:44.681498+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TYROBP as ready","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:02:44.670832+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyrobp has been classified as Red List (Low Evidence).","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:02:38.349822+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TYROBP were changed from  to polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1 MONDO:0020749","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:02:14.686075+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TYROBP were set to ","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:01:15.958104+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TYROBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:00:49.542688+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TYROBP as Red List (low evidence)","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T14:00:49.535974+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyrobp has been classified as Red List (Low Evidence).","entity_name":"TYROBP","entity_type":"gene"},{"created":"2025-11-26T13:59:15.978947+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFRSF11A as ready","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-11-26T13:59:15.967263+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf11a has been classified as Green List (High Evidence).","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-11-26T13:59:11.129106+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNFRSF11A were changed from  to Osteopetrosis, autosomal recessive 7 MIM#612301","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-11-26T13:58:42.708863+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFRSF11A were set to ","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-11-26T13:58:20.244863+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TNFRSF11A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-11-26T13:57:45.403233+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFB1 as ready","entity_name":"TGFB1","entity_type":"gene"},{"created":"2025-11-26T13:57:45.391867+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfb1 has been classified as Green List (High Evidence).","entity_name":"TGFB1","entity_type":"gene"},{"created":"2025-11-26T13:57:38.656141+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFB1 were changed from  to Camurati-Engelmann disease MONDO:0007542","entity_name":"TGFB1","entity_type":"gene"},{"created":"2025-11-26T13:57:10.879188+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFB1 were set to ","entity_name":"TGFB1","entity_type":"gene"},{"created":"2025-11-26T13:56:38.798988+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFB1","entity_type":"gene"},{"created":"2025-11-26T13:55:57.386366+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCIRG1 as ready","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2025-11-26T13:55:57.379070+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcirg1 has been classified as Green List (High Evidence).","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2025-11-26T13:55:51.858257+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCIRG1 were changed from  to Osteopetrosis, autosomal recessive 1 MIM#259700","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2025-11-26T13:55:25.422603+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCIRG1 were set to ","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2025-11-26T13:52:43.984403+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCIRG1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2025-11-26T13:51:58.022097+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SOST as ready","entity_name":"SOST","entity_type":"gene"},{"created":"2025-11-26T13:51:58.011687+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sost has been classified as Green List (High Evidence).","entity_name":"SOST","entity_type":"gene"},{"created":"2025-11-26T13:51:55.870751+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SOST were changed from  to sclerosteosis 1 MONDO:0010016","entity_name":"SOST","entity_type":"gene"},{"created":"2025-11-26T13:51:33.872466+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SOST were set to ","entity_name":"SOST","entity_type":"gene"},{"created":"2025-11-26T13:51:08.090593+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SOST was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SOST","entity_type":"gene"},{"created":"2025-11-26T13:50:18.692656+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNX10 as ready","entity_name":"SNX10","entity_type":"gene"},{"created":"2025-11-26T13:50:18.684990+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snx10 has been classified as Green List (High Evidence).","entity_name":"SNX10","entity_type":"gene"},{"created":"2025-11-26T13:50:15.700364+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNX10 were changed from  to Osteopetrosis, autosomal recessive 8 MIM#615085","entity_name":"SNX10","entity_type":"gene"},{"created":"2025-11-26T13:49:52.899524+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNX10 were set to ","entity_name":"SNX10","entity_type":"gene"},{"created":"2025-11-26T13:49:31.157993+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SNX10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNX10","entity_type":"gene"},{"created":"2025-11-26T13:48:54.116611+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTH1R as ready","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:48:54.105663+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pth1r has been classified as Green List (High Evidence).","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:48:50.637730+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTH1R were changed from  to Chondrodysplasia, Blomstrand type, MIM# 215045","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:48:27.944006+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PTH1R were set to ","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:48:02.161266+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PTH1R was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:47:37.301548+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PTH1R: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chondrodysplasia, Blomstrand type, MIM# 215045; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PTH1R","entity_type":"gene"},{"created":"2025-11-26T13:46:04.232729+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRP5 as ready","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:46:04.221004+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp5 has been classified as Green List (High Evidence).","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:46:01.494676+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP5 were changed from autosomal dominant osteopetrosis 1 MONDO:0011877 to autosomal dominant osteopetrosis 1 MONDO:0011877","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:45:43.618413+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP5 were changed from  to autosomal dominant osteopetrosis 1 MONDO:0011877","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:44:12.245368+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRP5 were set to ","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:43:48.283681+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LRP5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LRP5","entity_type":"gene"},{"created":"2025-11-26T13:34:42.994513+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IKBKG as ready","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:34:42.985505+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Green List (High Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:34:31.071380+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IKBKG were changed from  to IKBKG-related immunodeficiency with or without ectodermal dysplasia MONDO:0100162; incontinentia pigmenti MONDO:0010631","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:33:53.352359+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IKBKG were set to ","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:33:24.828251+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IKBKG was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:32:56.773377+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: IKBKG.","entity_name":"IKBKG","entity_type":"gene"},{"created":"2025-11-26T13:32:24.137494+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FERMT3 as ready","entity_name":"FERMT3","entity_type":"gene"},{"created":"2025-11-26T13:32:24.129750+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fermt3 has been classified as Green List (High Evidence).","entity_name":"FERMT3","entity_type":"gene"},{"created":"2025-11-26T13:32:20.411481+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FERMT3 were changed from  to leukocyte adhesion deficiency 3 MONDO:0013016","entity_name":"FERMT3","entity_type":"gene"},{"created":"2025-11-26T13:31:40.832741+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FERMT3 were set to ","entity_name":"FERMT3","entity_type":"gene"},{"created":"2025-11-26T13:31:13.042223+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FERMT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FERMT3","entity_type":"gene"},{"created":"2025-11-26T13:30:40.153977+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSK as ready","entity_name":"CTSK","entity_type":"gene"},{"created":"2025-11-26T13:30:40.143430+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsk has been classified as Green List (High Evidence).","entity_name":"CTSK","entity_type":"gene"},{"created":"2025-11-26T13:30:38.207025+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSK were changed from  to pycnodysostosis MONDO:0009940","entity_name":"CTSK","entity_type":"gene"},{"created":"2025-11-26T13:30:12.006395+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTSK were set to ","entity_name":"CTSK","entity_type":"gene"},{"created":"2025-11-26T13:29:48.991547+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTSK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSK","entity_type":"gene"},{"created":"2025-11-26T13:29:11.612354+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ANKH as ready","entity_name":"ANKH","entity_type":"gene"},{"created":"2025-11-26T13:29:11.599649+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ankh has been classified as Green List (High Evidence).","entity_name":"ANKH","entity_type":"gene"},{"created":"2025-11-26T13:29:09.209442+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ANKH were changed from  to craniometaphyseal dysplasia MONDO:0015465","entity_name":"ANKH","entity_type":"gene"},{"created":"2025-11-26T13:28:43.357175+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ANKH were set to ","entity_name":"ANKH","entity_type":"gene"},{"created":"2025-11-26T13:28:15.950277+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ANKH was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ANKH","entity_type":"gene"},{"created":"2025-11-26T13:25:52.717152+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AMER1 as ready","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:25:52.709306+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: amer1 has been classified as Green List (High Evidence).","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:25:48.885298+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AMER1 were changed from Osteopathia striata with cranial sclerosis\t300373; Osteopathia striata with cranial sclerosis 300373 to Osteopathia striata with cranial sclerosis, MIM# 300373","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:25:18.258871+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.358","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AMER1 were set to ","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:24:41.120308+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AMER1 as ready","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:24:41.111545+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: amer1 has been classified as Green List (High Evidence).","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:24:35.472141+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AMER1 were changed from  to Osteopathia striata with cranial sclerosis, MIM# 300373","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:23:54.333637+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AMER1 were set to ","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:23:33.307063+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AMER1 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:22:58.316458+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AMER1 as ready","entity_name":"AMER1","entity_type":"gene"},{"created":"2025-11-26T13:22:58.305835+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: amer1 has been classified as Green List (High Evidence).","entity_name":"AMER1","entity_type":"gene"}]}