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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=932",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}