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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=930",
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"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"
}
]
}