{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=930","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=928","results":[{"created":"2022-03-19T11:20:55.798281+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF4 were changed from  to Mitochondrial complex I deficiency, nuclear type 15 - MIM#618237","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:20:25.949252+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.390","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF4 were set to ","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:19:56.177517+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.389","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:19:26.283846+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.388","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF4 as Red List (low evidence)","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:19:26.272660+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.388","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:18:47.016345+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.730","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF4 as ready","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:18:47.006401+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.730","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Green List (High Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:18:43.428131+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.730","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF4 were changed from  to Mitochondrial complex I deficiency, nuclear type 15 - MIM#618237","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:18:04.466093+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF4 were set to ","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:17:26.987080+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:16:31.024624+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11554","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF4 as ready","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:16:31.003818+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11554","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Green List (High Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:16:23.296003+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11554","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF4 were changed from  to Mitochondrial complex I deficiency, nuclear type 15 - MIM#618237","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:16:03.681056+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11553","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF4 were set to ","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:15:42.526261+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11552","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:14:54.828909+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.425","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF3 as ready","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:14:54.803209+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.425","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf3 has been classified as Green List (High Evidence).","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:14:51.247137+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.425","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF3 were changed from  to Mitochondrial complex I deficiency, nuclear type 18 - MIM#618240","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:14:21.807256+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF3 were set to ","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:13:52.205348+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.423","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:13:09.091262+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.387","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF3 as ready","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:13:09.073866+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.387","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf3 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:13:05.636546+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.387","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF3 were changed from  to Mitochondrial complex I deficiency, nuclear type 18 - MIM#618240","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:12:34.907332+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF3 were set to ","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T11:12:01.751192+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.385","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T10:51:03.816828+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.384","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF3 as Amber List (moderate evidence)","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T10:51:03.807636+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.384","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf3 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-19T10:42:15.699135+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.21","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: EDARADD were changed from  to autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884; autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:38:24.307422+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.20","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDARADD were set to ","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:36:25.612721+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.19","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDARADD was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:35:49.218263+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.18","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: EDAR as ready","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:35:49.209108+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.18","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: edar has been classified as Green List (High Evidence).","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:35:14.263220+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.18","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: EDAR were changed from  to autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884; autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:34:39.851117+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.17","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDAR were set to 10431241; 20301291; 16435307; 20979233; 23401279; 18384562","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:34:19.999707+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.17","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDAR were set to ","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:33:51.853328+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.16","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDAR was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-19T10:33:13.036037+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.15","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: EDA as ready","entity_name":"EDA","entity_type":"gene"},{"created":"2022-03-19T10:33:13.024962+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.15","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: eda has been classified as Green List (High Evidence).","entity_name":"EDA","entity_type":"gene"},{"created":"2022-03-19T10:32:44.760760+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.15","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: EDA were changed from  to Ectodermal dysplasia 1, hypohidrotic, X-linked MIM#305100; Tooth agenesis, selective, X-linked 1 MIM#313500","entity_name":"EDA","entity_type":"gene"},{"created":"2022-03-19T10:32:15.188625+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.14","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDA were set to ","entity_name":"EDA","entity_type":"gene"},{"created":"2022-03-19T10:31:28.646802+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.13","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDA was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"EDA","entity_type":"gene"},{"created":"2022-03-19T10:30:48.975902+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.12","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: DSG1 as ready","entity_name":"DSG1","entity_type":"gene"},{"created":"2022-03-19T10:30:48.958006+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.12","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dsg1 has been classified as Green List (High Evidence).","entity_name":"DSG1","entity_type":"gene"},{"created":"2022-03-19T10:30:45.731905+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.12","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: DSG1 were changed from  to Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, AR (MIM#615508); Keratosis palmoplantaris striata I, AD (MIM# 148700)","entity_name":"DSG1","entity_type":"gene"},{"created":"2022-03-19T10:30:11.230237+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.11","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: DSG1 were set to ","entity_name":"DSG1","entity_type":"gene"},{"created":"2022-03-19T10:29:26.280897+11:00","panel_name":"Desmosomal disorders","panel_id":97,"panel_version":"0.10","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: DSG1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DSG1","entity_type":"gene"},{"created":"2022-03-19T10:22:16.997148+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11551","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: EDARADD as ready","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:22:16.986409+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11551","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: edaradd has been classified as Green List (High Evidence).","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:16:10.389117+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11551","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDARADD was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-19T10:06:58.174746+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11550","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: EDARADD: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301291, 34219261, 11780064, 26991760, 34573371, 20979233, 17354266, 26440664; Phenotypes: autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884, autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"EDARADD","entity_type":"gene"},{"created":"2022-03-18T20:44:42.831689+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11550","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: EDAR as ready","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T20:44:42.822133+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11550","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: edar has been classified as Green List (High Evidence).","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T20:40:37.017542+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11550","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: EDAR were changed from  to autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884; autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T20:38:06.022699+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11549","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDAR were set to ","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T20:29:21.082841+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11548","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDAR was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T20:26:36.615348+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11547","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: EDAR: Rating: GREEN; Mode of pathogenicity: None; Publications: 10431241, 20301291, 16435307, 20979233, 23401279, 18384562; Phenotypes: autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884, autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"EDAR","entity_type":"gene"},{"created":"2022-03-18T19:49:20.907568+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11547","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF3 as ready","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:49:20.895937+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11547","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf3 has been classified as Green List (High Evidence).","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:46:20.817367+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11547","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF3 were changed from  to Mitochondrial complex I deficiency, nuclear type 18 - MIM#618240","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:45:17.747484+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11546","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF3 were set to ","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:44:57.041901+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11545","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:42:26.430048+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.727","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF3 as ready","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T19:42:26.418426+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.727","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf3 has been classified as Green List (High Evidence).","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T18:42:15.441385+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.727","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF3 were changed from  to Mitochondrial complex I deficiency, nuclear type 18 - MIM#618240","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T18:41:44.125724+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.726","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF3 were set to ","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T18:40:12.056766+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF3","entity_type":"gene"},{"created":"2022-03-18T18:38:46.040892+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.246","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:38:46.030058+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.246","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:38:43.247552+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.246","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to ","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:38:31.222372+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from ?Mitochondrial complex I deficiency, nuclear type 13 618235; leukoencephalopathy to Mitochondrial complex I deficiency, nuclear type 13 618235; leukoencephalopathy","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:37:50.581911+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:37:50.570551+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Green List (High Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:37:47.847044+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from  to Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:37:16.901809+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to ","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:36:43.340766+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.420","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:36:05.742931+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.383","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:36:05.726251+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.383","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Green List (High Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:35:58.921700+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.383","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from  to Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:35:24.286691+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.382","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to ","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:34:47.592299+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.381","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:34:14.707144+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.380","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:33:27.079451+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.724","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:33:27.070208+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.724","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Green List (High Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:33:24.665311+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.724","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from  to Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:32:03.778946+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.723","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to ","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:31:26.322327+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:30:37.790911+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1492","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000; Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235 to Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235; Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:30:06.942600+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000 to Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000; Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:29:40.537954+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to 28857146; 18513682","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:28:48.040776+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:28:48.030260+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:28:43.424831+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA2 as Amber List (moderate evidence)","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:28:43.415020+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:27:48.315368+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11544","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA2 as ready","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:27:48.300214+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11544","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa2 has been classified as Green List (High Evidence).","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:27:20.554636+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11544","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA2 were changed from  to Mitochondrial complex I deficiency, nuclear type 13 - MIM#618235","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:26:59.923281+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11543","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA2 were set to ","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T18:26:38.805992+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11542","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA2","entity_type":"gene"},{"created":"2022-03-18T17:25:34.024156+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11541","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFB8: Rating: GREEN; Mode of pathogenicity: None; Publications: 29429571; Phenotypes: Mitochondrial complex I deficiency, nuclear type 32 - MIM#618252; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-18T17:25:30.437077+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.721","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFB8: Rating: GREEN; Mode of pathogenicity: None; Publications: 29429571; Phenotypes: Mitochondrial complex I deficiency, nuclear type 32 - MIM#618252; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFB8","entity_type":"gene"}]}