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{
"count": 220842,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1964",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1962",
"results": [
{
"created": "2020-01-25T12:12:10.813023+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdss2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:11:57.900653+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDSS2 were changed from to Coenzyme Q10 deficiency, primary, 3, MIM#614652",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:11:22.697138+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.415",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDSS2 were set to ",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:09:12.307469+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDSS2 as Amber List (moderate evidence)",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:09:12.299548+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdss2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:08:29.727867+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDSS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 17186472, 29032433; Phenotypes: Coenzyme Q10 deficiency, primary, 3, MIM#614652; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDSS2",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:04:04.386049+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAK1 as ready",
"entity_name": "PAK1",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:04:04.378553+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pak1 has been classified as Green List (High Evidence).",
"entity_name": "PAK1",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:03:54.942437+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PAK1 as Green List (high evidence)",
"entity_name": "PAK1",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:03:54.933452+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pak1 has been classified as Green List (High Evidence).",
"entity_name": "PAK1",
"entity_type": "gene"
},
{
"created": "2020-01-25T12:02:38.290582+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PAK1 was added\ngene: PAK1 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: PAK1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PAK1 were set to 30290153; 31504246\nPhenotypes for gene: PAK1 were set to Intellectual developmental disorder with macrocephaly, seizures, and speech delay (MIM 618158)\nReview for gene: PAK1 was set to GREEN\ngene: PAK1 was marked as current diagnostic\nAdded comment: Six unrelated individuals with de novo variants int his gene reported. \nSources: Expert list",
"entity_name": "PAK1",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:06:48.408200+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTX2 as ready",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:06:48.400586+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:06:35.060705+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTX2 were changed from to Microphthalmia, syndromic 5 610125",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:06:01.008292+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTX2 were set to ",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:05:27.063208+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:04:50.632348+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: OTX2 as Amber List (moderate evidence)",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:04:50.579370+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T09:04:15.714186+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 19965921, 15846561; Phenotypes: Microphthalmia, syndromic 5 610125; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:59:31.802503+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUBPL as ready",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:59:31.794867+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Amber List (Moderate Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:59:18.629729+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:58:45.163089+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUBPL were set to ",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:58:10.727569+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:57:35.263821+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NUBPL as Amber List (moderate evidence)",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:57:35.256333+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Amber List (Moderate Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:56:50.578342+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NUBPL: Rating: AMBER; Mode of pathogenicity: None; Publications: 23553477, 20818383; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:54:41.488338+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEDD4L as ready",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:54:41.480608+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nedd4l has been classified as Green List (High Evidence).",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:54:03.227205+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEDD4L were changed from to Periventricular nodular heterotopia 7, MIM#617201",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:53:28.813717+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.402",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEDD4L were set to ",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:52:54.582823+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEDD4L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:52:08.127190+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEDD4L: Rating: GREEN; Mode of pathogenicity: None; Publications: 28515470, 23934111, 28212375, 27694961; Phenotypes: Periventricular nodular heterotopia 7, MIM#617201; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:42:53.985386+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS7 as ready",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:42:53.978502+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:42:42.951627+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS7 were changed from to Leigh syndrome, MIM#256000",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:42:08.639840+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.399",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS7 were set to ",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:41:33.515769+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:40:59.077474+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFS7 as Amber List (moderate evidence)",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:40:59.066377+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:40:18.379002+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS7: Rating: AMBER; Mode of pathogenicity: None; Publications: 17604671, 17275378, 15269216; Phenotypes: Leigh syndrome, MIM#256000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:38:02.146270+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS6 as ready",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:38:02.138913+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:37:51.669920+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS6 were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:37:10.665348+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS6 were set to ",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:36:36.154943+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:35:58.189053+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFS6 as Amber List (moderate evidence)",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:35:58.178200+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:35:16.335338+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS6: Rating: AMBER; Mode of pathogenicity: None; Publications: 15372108, 19259137, 27290639; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:31:21.827357+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS1 as ready",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:31:21.819856+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:31:12.791800+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS1 were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:30:37.914228+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:30:01.485766+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFS1 as Amber List (moderate evidence)",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:30:01.477444+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:29:17.819265+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:26:34.999635+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF4 as ready",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:26:34.992268+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:26:21.782723+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF4 were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:25:47.556911+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF4 were set to ",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:25:13.956677+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.387",
"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": "2020-01-25T08:24:37.279425+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFAF4 as Amber List (moderate evidence)",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:24:37.272128+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:23:55.754504+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF4: Rating: AMBER; Mode of pathogenicity: None; Publications: 28853723, 19463981; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:21:29.451444+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF3 as ready",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:21:29.444041+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.385",
"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": "2020-01-25T08:21:19.906872+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF3 were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2020-01-25T08:20:44.380366+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.384",
"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": "2020-01-25T08:20:12.955698+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"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": "2020-01-25T08:20:12.944251+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"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": "2020-01-25T08:19:27.616544+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF3: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:40:10.353941+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO3A as ready",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:40:10.346438+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo3a has been classified as Green List (High Evidence).",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:40:01.215742+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO3A were changed from Deafness, autosomal recessive 30, MIM# 607101 to Deafness, autosomal recessive 30, MIM# 607101",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:39:19.570602+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO3A were changed from to Deafness, autosomal recessive 30, MIM# 607101",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:38:43.583260+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO3A were set to ",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:38:09.006258+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO3A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO3A",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:35:39.473106+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ESRP1 as ready",
"entity_name": "ESRP1",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:35:39.465887+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: esrp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ESRP1",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:34:56.971148+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GRAP as ready",
"entity_name": "GRAP",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:34:56.963311+11:00",
"panel_name": "Deafness",
"panel_id": 209,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grap has been classified as Red List (Low Evidence).",
"entity_name": "GRAP",
"entity_type": "gene"
},
{
"created": "2020-01-24T22:33:26.685457+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-24T21:37:17.863102+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS2 were changed from Mitochondrial complex I deficiency, MIM#252010 to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:37:11.889092+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS2 as ready",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:37:11.880440+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:36:46.491342+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS2 were changed from to Mitochondrial complex I deficiency, MIM#252010",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:36:15.950577+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS2 were set to ",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:35:27.540421+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:34:52.772521+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFS2 as Amber List (moderate evidence)",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:34:52.765690+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:34:10.059360+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 23266820, 22036843, 20819849; Phenotypes: Mitochondrial complex I deficiency, MIM#252010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:27:52.903210+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA6 as ready",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:27:52.895909+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa6 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:27:47.207734+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA6 were changed from Mitochondrial complex I deficiency, nuclear type 33, MIM#618253 to Mitochondrial complex I deficiency, nuclear type 33, MIM#618253",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:27:06.394244+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA6 were changed from to Mitochondrial complex I deficiency, nuclear type 33, MIM#618253",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:26:31.361161+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFA6 were set to ",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:25:27.613970+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFA6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:24:51.668121+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFA6 as Red List (low evidence)",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:24:51.660882+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa6 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA6",
"entity_type": "gene"
},
{
"created": "2020-01-24T21:24:09.050030+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFA6: Rating: RED; Mode of pathogenicity: None; Publications: 30245030; Phenotypes: Mitochondrial complex I deficiency, nuclear type 33, MIM#618253; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA6",
"entity_type": "gene"
}
]
}