{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=932","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=930","results":[{"created":"2022-03-18T07:29:03.317932+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11519","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IGLL1 were set to ","entity_name":"IGLL1","entity_type":"gene"},{"created":"2022-03-18T07:28:42.618867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11518","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IGLL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IGLL1","entity_type":"gene"},{"created":"2022-03-18T07:28:20.594086+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11517","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IGLL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9419212, 25502423, 27576013; Phenotypes: Agammaglobulinaemia 2, MIM# 613500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IGLL1","entity_type":"gene"},{"created":"2022-03-18T07:16:36.409348+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11517","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IGHMBP2 as ready","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-18T07:16:36.397196+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11517","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ighmbp2 has been classified as Green List (High Evidence).","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-18T07:16:27.402009+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11517","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IGHMBP2 were changed from  to Neuronopathy, distal hereditary motor, type VI, MIM# 604320; Charcot-Marie-Tooth disease, axonal, type 2S, MIM# 616155","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-18T07:15:59.840759+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11516","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IGHMBP2 were set to ","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-18T07:15:40.426014+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11515","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IGHMBP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-18T07:15:19.707633+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11514","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IGHMBP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neuronopathy, distal hereditary motor, type VI, MIM# 604320, Charcot-Marie-Tooth disease, axonal, type 2S, MIM# 616155; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2022-03-17T20:19:20.621761+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC134 as ready","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:19:20.609733+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc134 has been classified as Green List (High Evidence).","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:19:17.888084+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC134 were changed from  to Osteogenesis imperfecta, type XXII, MIM#619795","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:16:16.792356+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC134 as Green List (high evidence)","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:16:16.763309+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc134 has been classified as Green List (High Evidence).","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:15:33.078407+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11514","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC134 as ready","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:15:33.069065+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc134 has been classified as Green List (High Evidence).","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:15:23.689075+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11514","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC134 as Green List (high evidence)","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:15:23.680522+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc134 has been classified as Green List (High Evidence).","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:15:04.551671+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11513","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CCDC134 was added\ngene: CCDC134 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: CCDC134 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CCDC134 were set to 32181939; 34204301; 35019224\nPhenotypes for gene: CCDC134 were set to Osteogenesis imperfecta, type XXII, MIM#619795\nReview for gene: CCDC134 was set to GREEN\nAdded comment: Three unrelated families reported. \nSources: Expert list","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:14:37.014439+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CCDC134: Changed phenotypes: Osteogenesis imperfecta, type XXII, MIM#619795","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:12:36.899629+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CCDC134 was added\ngene: CCDC134 was added to Osteogenesis Imperfecta. Sources: Expert list\nMode of inheritance for gene: CCDC134 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CCDC134 were set to 32181939; 34204301; 35019224\nReview for gene: CCDC134 was set to GREEN\nAdded comment: Three unrelated families reported. \nSources: Expert list","entity_name":"CCDC134","entity_type":"gene"},{"created":"2022-03-17T20:08:59.867925+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11512","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RACGAP1 as ready","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:08:59.856323+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: racgap1 has been classified as Red List (Low Evidence).","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:07:59.564529+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11512","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RACGAP1 was added\ngene: RACGAP1 was added to Mendeliome. Sources: Expert Review\nMode of inheritance for gene: RACGAP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RACGAP1 were set to 34818416\nPhenotypes for gene: RACGAP1 were set to Anaemia, congenital dyserythropoietic, type IIIb, autosomal recessive 619789\nReview for gene: RACGAP1 was set to RED\nAdded comment: Single affected individual reported. \nSources: Expert Review","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:06:26.845546+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RACGAP1 as ready","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:06:26.833433+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: racgap1 has been classified as Red List (Low Evidence).","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:06:10.785411+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.15","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RACGAP1 was added\ngene: RACGAP1 was added to Red cell disorders. Sources: Expert list\nMode of inheritance for gene: RACGAP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RACGAP1 were set to 34818416\nPhenotypes for gene: RACGAP1 were set to Anaemia, congenital dyserythropoietic, type IIIb, autosomal recessive\t619789\nReview for gene: RACGAP1 was set to RED\nAdded comment: Single affected individual reported. \nSources: Expert list","entity_name":"RACGAP1","entity_type":"gene"},{"created":"2022-03-17T20:01:54.666268+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.14","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF23 were changed from Congenital dyserythropoietic anemia type III to Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:01:45.762084+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.13","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF23 were set to 23570799","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:01:36.478483+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF23 as Amber List (moderate evidence)","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:01:36.469196+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif23 has been classified as Amber List (Moderate Evidence).","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:01:25.263159+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.11","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KIF23: Added comment: Second individual reported, elongation variant.; Changed rating: AMBER; Changed phenotypes: Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:00:43.043325+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11511","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF23 were changed from Congenital dyserythropoietic anemia to Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T20:00:14.861129+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11510","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF23 were set to 23570799","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:59:38.679202+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11509","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF23 as Amber List (moderate evidence)","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:59:38.667733+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11509","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif23 has been classified as Amber List (Moderate Evidence).","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:59:19.762937+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11508","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KIF23: Added comment: Second individual reported, elongation variant.; Changed rating: AMBER; Changed publications: 23570799, 33159567; Changed phenotypes: Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:56:25.957990+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF23 were changed from Anaemia, congenital dyserythropoietic, type IIIA 105600 to Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:56:01.409754+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF23 were changed from Congenital dyserythropoietic anemia type III to Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:55:37.188179+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF23 were set to 23570799","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:53:53.580756+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.11","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF23 as Amber List (moderate evidence)","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:53:53.569776+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif23 has been classified as Amber List (Moderate Evidence).","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T19:53:19.303078+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.10","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KIF23: Added comment: Second individual reported, elongation variant.; Changed rating: AMBER; Changed publications: 23570799, 33159567; Changed phenotypes: Anaemia, congenital dyserythropoietic, type IIIA 105600","entity_name":"KIF23","entity_type":"gene"},{"created":"2022-03-17T18:50:21.857673+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL12RB1 as ready","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:50:21.846811+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il12rb1 has been classified as Green List (High Evidence).","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:50:19.170928+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL12RB1 were changed from  to Immunodeficiency 30, MIM# 614891","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:43:01.695292+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL12RB1 were set to ","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:42:31.091239+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL12RB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:42:00.590267+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL12RB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9603733, 9603732, 12591909, 15736007, 23864330; Phenotypes: Immunodeficiency 30, MIM# 614891; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:31:36.190025+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11508","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL12RB1 as ready","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:31:36.175179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il12rb1 has been classified as Green List (High Evidence).","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:31:21.565363+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11508","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL12RB1 were changed from  to Immunodeficiency 30, MIM# 614891","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:31:01.734176+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11507","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL12RB1 were set to ","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:30:37.619855+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11506","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL12RB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:30:12.799939+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11505","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL12RB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9603733, 9603732, 12591909, 15736007, 23864330,; Phenotypes: Immunodeficiency 30, MIM# 614891; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL12RB1","entity_type":"gene"},{"created":"2022-03-17T18:27:30.304860+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11505","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL13 as ready","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:27:30.294653+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il13 has been classified as Red List (Low Evidence).","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:27:22.514448+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11505","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL13 were changed from  to {Allergic rhinitis, susceptibility to} 607154; {Asthma, susceptibility to} 600807","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:27:00.222877+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11504","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL13 as Red List (low evidence)","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:27:00.189888+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il13 has been classified as Red List (Low Evidence).","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:26:42.748041+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11503","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL13: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Allergic rhinitis, susceptibility to} 607154, {Asthma, susceptibility to} 600807; Mode of inheritance: None","entity_name":"IL13","entity_type":"gene"},{"created":"2022-03-17T18:24:46.594201+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:24:46.583163+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Green List (High Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:24:43.679365+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from  to Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:24:15.041416+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.418","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:23:45.469602+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.417","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:23:15.446758+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.416","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:22:13.689986+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:22:13.680671+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Green List (High Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:22:09.171265+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from  to Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:21:29.509702+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:20:53.170125+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:20:07.143587+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:19:00.621196+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.380","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:19:00.606106+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.380","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:16:34.293765+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.380","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from  to Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:16:05.093330+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:15:21.997242+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.378","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:14:53.888339+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.377","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF2 as Red List (low evidence)","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:14:53.874806+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.377","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:14:24.261170+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.376","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: RED; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:13:31.499786+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.721","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:13:31.487370+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.721","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Green List (High Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:13:28.799010+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.721","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from  to Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:12:50.190228+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:12:12.258341+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.719","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:11:33.844169+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:10:33.555091+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:10:33.545778+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Green List (High Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:10:26.019319+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11503","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from  to Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:09:58.700753+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11502","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:07:36.874940+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T18:07:03.960573+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.376","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF1 as ready","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:07:03.950770+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.376","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:06:54.944385+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.376","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF1 were changed from  to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:06:22.044198+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.375","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF1 were set to ","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:05:42.780183+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.374","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:05:14.444853+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.373","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF1 as Red List (low evidence)","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:05:14.434077+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.373","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:04:43.768158+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.372","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: RED; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"}]}