{"count":220842,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1964","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}