{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=363","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=361","results":[{"created":"2024-10-21T16:17:37.901116+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: KIAA0586: Rating: GREEN; Mode of pathogenicity: None; Publications: 26096313; Phenotypes: Joubert syndrome 23 MIM#616490; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2024-10-21T15:33:41.331751+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: KDM6A: Rating: GREEN; Mode of pathogenicity: None; Publications: 33674768; Phenotypes: Kabuki syndrome 2 MONDO:0010465; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"KDM6A","entity_type":"gene"},{"created":"2024-10-21T15:30:42.797759+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: KCTD7: Rating: GREEN; Mode of pathogenicity: None; Publications: 30295347, 31197948; Phenotypes: progressive myoclonus epilepsy MONDO:0020074; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KCTD7","entity_type":"gene"},{"created":"2024-10-21T11:02:38.725672+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NAXE as ready","entity_name":"NAXE","entity_type":"gene"},{"created":"2024-10-21T11:02:38.703353+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: naxe has been classified as Green List (High Evidence).","entity_name":"NAXE","entity_type":"gene"},{"created":"2024-10-21T11:02:31.712571+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NAXE as Green List (high evidence)","entity_name":"NAXE","entity_type":"gene"},{"created":"2024-10-21T11:02:31.696237+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: naxe has been classified as Green List (High Evidence).","entity_name":"NAXE","entity_type":"gene"},{"created":"2024-10-21T11:01:18.391227+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NAXE was added\ngene: NAXE was added to Regression. Sources: Expert Review\nMode of inheritance for gene: NAXE was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NAXE were set to 27122014; 27616477; 31758406\nPhenotypes for gene: NAXE were set to Encephalopathy, progressive, early-onset, with brain oedema and/or leukoencephalopathy, MIM# 617186\nReview for gene: NAXE was set to GREEN\nAdded comment: Early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy-1 (PEBEL1) is an autosomal recessive severe neurometabolic disorder characterized by rapidly progressive neurologic deterioration that is usually associated with a febrile illness. Affected infants tend to show normal early development followed by acute psychomotor regression with ataxia, hypotonia, respiratory insufficiency, and seizures, resulting in coma and death in the first years of life. Brain imaging shows multiple abnormalities, including brain edema and signal abnormalities in the cortical and subcortical regions. More than 5 unrelated families reported. \nSources: Expert Review","entity_name":"NAXE","entity_type":"gene"},{"created":"2024-10-21T09:43:15.387897+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: KCNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23086397, 24029078; Phenotypes: childhood-onset epilepsy syndrome MONDO:0020072; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KCNT1","entity_type":"gene"},{"created":"2024-10-21T08:44:13.725800+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: IVD: Rating: GREEN; Mode of pathogenicity: None; Publications: 26018748; Phenotypes: isovaleric acidemia MONDO:0009475; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IVD","entity_type":"gene"},{"created":"2024-10-21T08:39:04.569757+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"reviewed gene: ITPR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27108797, 27108798, 15623688, 22986007, 28488678; Phenotypes: aniridia-cerebellar ataxia-intellectual disability syndrome MONDO:0008795, spinocerebellar ataxia type 29 MONDO:0007298; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ITPR1","entity_type":"gene"},{"created":"2024-10-20T18:04:37.408849+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6528","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSL2 were changed from Neurodevelopmental disorder, MONDO:0700092, MSL2-related to Karayol-Borroto-Haghshenas neurodevelopmental syndrome, MIM# 620985","entity_name":"MSL2","entity_type":"gene"},{"created":"2024-10-20T18:03:52.300227+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6527","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MSL2: Changed phenotypes: Karayol-Borroto-Haghshenas neurodevelopmental syndrome, MIM# 620985","entity_name":"MSL2","entity_type":"gene"},{"created":"2024-10-20T18:03:33.368433+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2068","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSL2 were changed from Neurodevelopmental disorder, MONDO:0700092, MSL2-related to Karayol-Borroto-Haghshenas neurodevelopmental syndrome, MIM# 620985","entity_name":"MSL2","entity_type":"gene"},{"created":"2024-10-20T18:03:07.491088+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2067","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MSL2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Karayol-Borroto-Haghshenas neurodevelopmental syndrome, MIM# 620985; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSL2","entity_type":"gene"},{"created":"2024-10-20T18:02:22.149756+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WFDC2 were changed from bronchiectasis, MONDO:0004822, WFDC2-related to Bronchiectasis and nasal polyposis, MIM# 620984","entity_name":"WFDC2","entity_type":"gene"},{"created":"2024-10-20T18:01:44.194586+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WFDC2: Changed phenotypes: Bronchiectasis and nasal polyposis, MIM# 620984","entity_name":"WFDC2","entity_type":"gene"},{"created":"2024-10-20T18:01:04.285169+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2067","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WFDC2 were changed from bronchiectasis, MONDO:0004822, WFDC2-related to Bronchiectasis and nasal polyposis, MIM# 620984","entity_name":"WFDC2","entity_type":"gene"},{"created":"2024-10-20T18:00:24.871502+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2066","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WFDC2: Changed phenotypes: Bronchiectasis and nasal polyposis, MIM# 620984","entity_name":"WFDC2","entity_type":"gene"},{"created":"2024-10-20T17:56:39.085473+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BORCS8 were changed from Neurodevelopmental disorder (MONDO#0700092), BORCS8-related to Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:56:20.142356+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.314","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BORCS8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:56:00.615360+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6527","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BORCS8 were changed from Neurodevelopmental disorder (MONDO#0700092), BORCS8-related to Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:55:15.025493+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6526","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BORCS8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:52:53.091823+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.566","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BORCS8 were changed from Neurodevelopmental disorder (MONDO#0700092), BORCS8-related to Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:52:09.158193+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BORCS8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:51:50.823790+11:00","panel_name":"Optic Atrophy","panel_id":149,"panel_version":"1.43","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BORCS8 were changed from Neurodevelopmental disorder (MONDO#0700092), BORCS8-related to Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:51:09.302057+11:00","panel_name":"Optic Atrophy","panel_id":149,"panel_version":"1.42","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BORCS8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:50:09.149029+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2066","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BORCS8 were changed from Neurodevelopmental disorder (MONDO#0700092), BORCS8-related to Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:49:42.317334+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2065","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BORCS8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities, MIM# 620987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BORCS8","entity_type":"gene"},{"created":"2024-10-20T17:48:33.851122+11:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.76","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COPG1 were changed from Combined immunodeficiency MONDO:0015131, COPG1-related to Immunodeficiency 128, MIM# 620983","entity_name":"COPG1","entity_type":"gene"},{"created":"2024-10-20T17:47:51.493153+11:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.75","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: COPG1: Changed phenotypes: Immunodeficiency 128, MIM# 620983","entity_name":"COPG1","entity_type":"gene"},{"created":"2024-10-20T17:47:32.127228+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2065","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COPG1 were changed from Combined immunodeficiency MONDO:0015131, COPG1-related to Immunodeficiency 128, MIM# 620983","entity_name":"COPG1","entity_type":"gene"},{"created":"2024-10-20T17:47:02.559815+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2064","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: COPG1: Changed phenotypes: Immunodeficiency 128, MIM#  620983","entity_name":"COPG1","entity_type":"gene"},{"created":"2024-10-20T17:33:22.459257+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.470","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: WDR60 as ready","entity_name":"WDR60","entity_type":"gene"},{"created":"2024-10-20T17:33:22.443741+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.470","user_name":"Lilian Downie","item_type":"entity","text":"Gene: wdr60 has been classified as Green List (High Evidence).","entity_name":"WDR60","entity_type":"gene"},{"created":"2024-10-20T17:33:15.512406+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.470","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: WDR60 were set to ","entity_name":"WDR60","entity_type":"gene"},{"created":"2024-10-20T17:32:21.937151+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.469","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: YARS2 as ready","entity_name":"YARS2","entity_type":"gene"},{"created":"2024-10-20T17:32:21.927550+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.469","user_name":"Lilian Downie","item_type":"entity","text":"Gene: yars2 has been classified as Green List (High Evidence).","entity_name":"YARS2","entity_type":"gene"},{"created":"2024-10-20T17:32:13.523656+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.469","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: YARS2 were set to ","entity_name":"YARS2","entity_type":"gene"},{"created":"2024-10-20T17:23:58.102905+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.468","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ZFYVE26 as ready","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2024-10-20T17:23:58.085375+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.468","user_name":"Lilian Downie","item_type":"entity","text":"Gene: zfyve26 has been classified as Green List (High Evidence).","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2024-10-20T17:23:52.416500+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.468","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ZFYVE26 were set to ","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2024-10-20T17:22:55.340336+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.467","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: AGBL5 as ready","entity_name":"AGBL5","entity_type":"gene"},{"created":"2024-10-20T17:22:55.322329+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.467","user_name":"Lilian Downie","item_type":"entity","text":"Gene: agbl5 has been classified as Green List (High Evidence).","entity_name":"AGBL5","entity_type":"gene"},{"created":"2024-10-20T17:22:51.059007+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.467","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: AGBL5 were changed from Retinitis pigmentosa 75, 617023 (3), Autosomal recessive to Retinitis pigmentosa 75, 617023","entity_name":"AGBL5","entity_type":"gene"},{"created":"2024-10-20T17:22:38.837789+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.466","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: AGBL5 were set to ","entity_name":"AGBL5","entity_type":"gene"},{"created":"2024-10-20T17:21:30.506290+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.465","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: AGT as ready","entity_name":"AGT","entity_type":"gene"},{"created":"2024-10-20T17:21:30.495036+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.465","user_name":"Lilian Downie","item_type":"entity","text":"Gene: agt has been classified as Green List (High Evidence).","entity_name":"AGT","entity_type":"gene"},{"created":"2024-10-20T17:21:25.409871+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.465","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: AGT were set to ","entity_name":"AGT","entity_type":"gene"},{"created":"2024-10-20T17:20:22.030546+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.464","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: AIMP1 as ready","entity_name":"AIMP1","entity_type":"gene"},{"created":"2024-10-20T17:20:22.017947+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.464","user_name":"Lilian Downie","item_type":"entity","text":"Gene: aimp1 has been classified as Green List (High Evidence).","entity_name":"AIMP1","entity_type":"gene"},{"created":"2024-10-20T17:20:16.535944+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.464","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: AIMP1 were set to ","entity_name":"AIMP1","entity_type":"gene"},{"created":"2024-10-20T17:19:17.868881+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.463","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ASL as ready","entity_name":"ASL","entity_type":"gene"},{"created":"2024-10-20T17:19:17.851090+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.463","user_name":"Lilian Downie","item_type":"entity","text":"Gene: asl has been classified as Green List (High Evidence).","entity_name":"ASL","entity_type":"gene"},{"created":"2024-10-20T17:19:12.977285+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.463","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ASL were set to ","entity_name":"ASL","entity_type":"gene"},{"created":"2024-10-20T17:18:20.734895+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.462","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ATCAY as ready","entity_name":"ATCAY","entity_type":"gene"},{"created":"2024-10-20T17:18:20.723714+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.462","user_name":"Lilian Downie","item_type":"entity","text":"Gene: atcay has been classified as Green List (High Evidence).","entity_name":"ATCAY","entity_type":"gene"},{"created":"2024-10-20T17:18:14.184165+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.462","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ATCAY were set to ","entity_name":"ATCAY","entity_type":"gene"},{"created":"2024-10-20T17:16:41.820677+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.461","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CDC45 as ready","entity_name":"CDC45","entity_type":"gene"},{"created":"2024-10-20T17:16:41.807807+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.461","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cdc45 has been classified as Green List (High Evidence).","entity_name":"CDC45","entity_type":"gene"},{"created":"2024-10-20T17:16:37.817413+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.461","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: CDC45 were changed from Meier-Gorlin syndrome 7, 617063 (3), Autosomal recessive to Meier-Gorlin syndrome 7, 617063","entity_name":"CDC45","entity_type":"gene"},{"created":"2024-10-20T17:16:22.502059+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.460","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CDC45 were set to ","entity_name":"CDC45","entity_type":"gene"},{"created":"2024-10-20T17:15:09.931185+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.459","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CHAT as ready","entity_name":"CHAT","entity_type":"gene"},{"created":"2024-10-20T17:15:09.906915+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.459","user_name":"Lilian Downie","item_type":"entity","text":"Gene: chat has been classified as Green List (High Evidence).","entity_name":"CHAT","entity_type":"gene"},{"created":"2024-10-20T17:15:04.679226+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.459","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CHAT were set to ","entity_name":"CHAT","entity_type":"gene"},{"created":"2024-10-20T17:14:03.797650+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.458","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CIT as ready","entity_name":"CIT","entity_type":"gene"},{"created":"2024-10-20T17:14:03.782127+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.458","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cit has been classified as Green List (High Evidence).","entity_name":"CIT","entity_type":"gene"},{"created":"2024-10-20T17:13:58.233826+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.458","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CIT were set to ","entity_name":"CIT","entity_type":"gene"},{"created":"2024-10-20T17:13:04.691793+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.457","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CNTNAP2 as ready","entity_name":"CNTNAP2","entity_type":"gene"},{"created":"2024-10-20T17:13:04.677174+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.457","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cntnap2 has been classified as Green List (High Evidence).","entity_name":"CNTNAP2","entity_type":"gene"},{"created":"2024-10-20T17:13:00.723989+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.457","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, 610042 (3) to Pitt-Hopkins like syndrome 1 MIM#610042","entity_name":"CNTNAP2","entity_type":"gene"},{"created":"2024-10-20T17:12:32.074879+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.456","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CNTNAP2 were set to ","entity_name":"CNTNAP2","entity_type":"gene"},{"created":"2024-10-20T17:11:33.869190+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: COG5 as ready","entity_name":"COG5","entity_type":"gene"},{"created":"2024-10-20T17:11:33.864523+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Added comment: Comment when marking as ready: Upgrade to green","entity_name":"COG5","entity_type":"gene"},{"created":"2024-10-20T17:11:33.822548+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cog5 has been classified as Red List (Low Evidence).","entity_name":"COG5","entity_type":"gene"},{"created":"2024-10-20T17:11:22.544313+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Tag for review tag was added to gene: COG5.","entity_name":"COG5","entity_type":"gene"},{"created":"2024-10-20T17:09:20.476904+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CABP4 as ready","entity_name":"CABP4","entity_type":"gene"},{"created":"2024-10-20T17:09:20.462024+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cabp4 has been classified as Green List (High Evidence).","entity_name":"CABP4","entity_type":"gene"},{"created":"2024-10-20T17:07:22.158626+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CABP4 were set to 16960802; 19074807; 20157620","entity_name":"CABP4","entity_type":"gene"},{"created":"2024-10-20T17:07:19.595901+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.455","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CABP4 were set to ","entity_name":"CABP4","entity_type":"gene"},{"created":"2024-10-20T17:06:30.438959+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.454","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CAPN3 as ready","entity_name":"CAPN3","entity_type":"gene"},{"created":"2024-10-20T17:06:30.422275+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.454","user_name":"Lilian Downie","item_type":"entity","text":"Gene: capn3 has been classified as Green List (High Evidence).","entity_name":"CAPN3","entity_type":"gene"},{"created":"2024-10-20T17:06:20.466783+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.454","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CAPN3 were set to ","entity_name":"CAPN3","entity_type":"gene"},{"created":"2024-10-20T17:05:09.305564+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.453","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CLPP as ready","entity_name":"CLPP","entity_type":"gene"},{"created":"2024-10-20T17:05:09.293333+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.453","user_name":"Lilian Downie","item_type":"entity","text":"Gene: clpp has been classified as Green List (High Evidence).","entity_name":"CLPP","entity_type":"gene"},{"created":"2024-10-20T17:05:04.372198+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.453","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CLPP were set to ","entity_name":"CLPP","entity_type":"gene"},{"created":"2024-10-20T17:03:29.523777+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.452","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: DNAAF5 as ready","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2024-10-20T17:03:29.478196+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.452","user_name":"Lilian Downie","item_type":"entity","text":"Gene: dnaaf5 has been classified as Green List (High Evidence).","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2024-10-20T17:03:23.229268+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.452","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: DNAAF5 were set to ","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2024-10-20T17:02:36.621498+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.451","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: COL11A1 as ready","entity_name":"COL11A1","entity_type":"gene"},{"created":"2024-10-20T17:02:36.605005+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.451","user_name":"Lilian Downie","item_type":"entity","text":"Gene: col11a1 has been classified as Green List (High Evidence).","entity_name":"COL11A1","entity_type":"gene"},{"created":"2024-10-20T17:02:21.766240+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.451","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: COL11A1 were set to ","entity_name":"COL11A1","entity_type":"gene"},{"created":"2024-10-20T17:01:27.838231+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.450","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CRLF1 as ready","entity_name":"CRLF1","entity_type":"gene"},{"created":"2024-10-20T17:01:27.822463+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.450","user_name":"Lilian Downie","item_type":"entity","text":"Gene: crlf1 has been classified as Green List (High Evidence).","entity_name":"CRLF1","entity_type":"gene"},{"created":"2024-10-20T17:01:25.214541+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.450","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CRLF1 were set to 12509788; 17436251; 17436252","entity_name":"CRLF1","entity_type":"gene"},{"created":"2024-10-20T17:01:24.945720+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.450","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CRLF1 were set to 12509788; 17436251; 17436252","entity_name":"CRLF1","entity_type":"gene"},{"created":"2024-10-20T17:01:18.898752+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.449","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CRLF1 were set to ","entity_name":"CRLF1","entity_type":"gene"},{"created":"2024-10-20T17:00:20.697166+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.448","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CTC1 as ready","entity_name":"CTC1","entity_type":"gene"},{"created":"2024-10-20T17:00:20.685046+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.448","user_name":"Lilian Downie","item_type":"entity","text":"Gene: ctc1 has been classified as Green List (High Evidence).","entity_name":"CTC1","entity_type":"gene"},{"created":"2024-10-20T17:00:09.734489+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.448","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CTC1 were set to ","entity_name":"CTC1","entity_type":"gene"}]}