{"count":220842,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1969","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1967","results":[{"created":"2020-01-22T22:02:02.438799+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GLYCTK: Rating: GREEN; Mode of pathogenicity: None; Publications: 3588091, 30637540, 28462797, 20949620, 28190537; Phenotypes: D-glyceric aciduria, MIM# 220120; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLYCTK","entity_type":"gene"},{"created":"2020-01-22T21:43:46.888876+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FUT8 as ready","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:43:46.877089+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fut8 has been classified as Green List (High Evidence).","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:43:37.313594+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FUT8 as Green List (high evidence)","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:43:37.298899+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fut8 has been classified as Green List (High Evidence).","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:42:29.519120+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FUT8 was added\ngene: FUT8 was added to Congenital Disorders of Glycosylation. Sources: Expert list\nMode of inheritance for gene: FUT8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUT8 were set to 29304374\nPhenotypes for gene: FUT8 were set to Congenital disorder of glycosylation with defective fucosylation, 618005\nReview for gene: FUT8 was set to GREEN\ngene: FUT8 was marked as current diagnostic\nAdded comment: Three unrelated individuals reported. \nSources: Expert list","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:42:04.091174+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FUT8 as ready","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:42:03.475826+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fut8 has been classified as Green List (High Evidence).","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:41:05.784771+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FUT8 as Green List (high evidence)","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:41:05.773193+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fut8 has been classified as Green List (High Evidence).","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:40:13.033208+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.293","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FUT8 was added\ngene: FUT8 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: FUT8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUT8 were set to 29304374\nPhenotypes for gene: FUT8 were set to Congenital disorder of glycosylation with defective fucosylation, 618005\nReview for gene: FUT8 was set to GREEN\ngene: FUT8 was marked as current diagnostic\nAdded comment: Three unrelated individuals, all had seizures as part of the phenotype. \nSources: Expert list","entity_name":"FUT8","entity_type":"gene"},{"created":"2020-01-22T21:37:34.741447+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.292","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXRED1 were set to 20858599; 20818383; 31434271","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:37:15.149549+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXRED1 as ready","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:37:14.409620+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxred1 has been classified as Green List (High Evidence).","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:37:05.079161+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXRED1 were set to 20858599, 20818383; 31434271","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:36:35.081038+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXRED1 were changed from Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000 to Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:36:04.725960+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.290","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXRED1 were changed from  to Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:35:34.367833+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.290","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXRED1 were set to ","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:35:02.192931+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.289","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXRED1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:34:02.648481+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.288","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FOXRED1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20858599, 20818383, 31434271; Phenotypes: Leigh syndrome due to mitochondrial complex I deficiency, MIM#256000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FOXRED1","entity_type":"gene"},{"created":"2020-01-22T21:27:31.357362+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.288","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKRP as ready","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:27:31.345961+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.288","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkrp has been classified as Amber List (Moderate Evidence).","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:27:26.280841+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.288","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKRP were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, MIM#613153 to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, MIM#613153","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:26:58.218261+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.287","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKRP were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, MIM#613153","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:26:22.359745+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.286","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FKRP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:25:48.844739+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.285","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FKRP as Amber List (moderate evidence)","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:25:48.832261+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.285","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkrp has been classified as Amber List (Moderate Evidence).","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:25:08.513886+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.284","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FKRP: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5, MIM#613153; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-22T21:21:32.546936+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.284","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FIG4 as ready","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:21:32.533767+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.284","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Red List (Low Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:21:32.348335+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.284","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FIG4 were changed from Polymicrogyria, bilateral temporooccipital, MIM#612691 to Polymicrogyria, bilateral temporooccipital, MIM#612691","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:21:02.190716+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.283","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FIG4 were changed from  to Polymicrogyria, bilateral temporooccipital, MIM#612691","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:20:31.809114+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.283","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FIG4 were set to ","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:19:53.165170+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.282","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FIG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:19:09.526897+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.281","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FIG4 as Red List (low evidence)","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:19:09.515039+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.281","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Red List (Low Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:18:28.947831+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FIG4: Rating: RED; Mode of pathogenicity: None; Publications: 24598713; Phenotypes: Polymicrogyria, bilateral temporooccipital, MIM#612691; Mode of inheritance: None","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-01-22T21:14:16.956510+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FH as ready","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:14:16.945158+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fh has been classified as Green List (High Evidence).","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:14:11.118142+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FH were changed from Fumarase deficiency, MIM#606812 to Fumarase deficiency, MIM#606812","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:13:41.887568+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.279","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FH were changed from  to Fumarase deficiency, MIM#606812","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:13:17.328138+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.279","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FH were set to 20301679; 10805328; 20549362; 15221078; 16151915","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:12:53.704583+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FH were set to ","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:12:29.194437+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T21:11:48.137045+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FH: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301679, 10805328, 20549362, 15221078, 16151915; Phenotypes: Fumarase deficiency, MIM#606812; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FH","entity_type":"gene"},{"created":"2020-01-22T20:25:05.561013+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR3 as ready","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:25:05.548046+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:24:54.855145+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR3 were changed from Hypochondroplasia, MIM#146000 to Hypochondroplasia, MIM#146000","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:20:14.969961+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.276","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR3 were changed from Hypochondroplasia, MIM#146000 to Hypochondroplasia, MIM#146000","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:19:33.278177+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.275","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR3 were changed from  to Hypochondroplasia, MIM#146000","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:18:57.143328+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.274","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGFR3 were set to ","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:18:19.069073+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.273","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:17:36.927787+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGFR3: Rating: GREEN; Mode of pathogenicity: None; Publications: 24630288, 27485793, 23649205, 12794698; Phenotypes: Hypochondroplasia, MIM#146000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-01-22T20:14:27.668170+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FDFT1 as ready","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:14:27.662939+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two unrelated families, functional data; seizures were a presenting feature.","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:14:27.633742+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdft1 has been classified as Green List (High Evidence).","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:13:40.660971+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FDFT1 were changed from  to Squalene synthase deficiency, MIM# 618156","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:13:11.162566+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FDFT1 were set to ","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:12:40.762980+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FDFT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:12:10.745674+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FDFT1 as Green List (high evidence)","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:12:10.733432+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdft1 has been classified as Green List (High Evidence).","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:10:19.435947+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FDFT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 29909962; Phenotypes: Squalene synthase deficiency, MIM# 618156; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FDFT1","entity_type":"gene"},{"created":"2020-01-22T20:05:14.423254+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FBXO11 as ready","entity_name":"FBXO11","entity_type":"gene"},{"created":"2020-01-22T20:05:14.411723+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbxo11 has been classified as Green List (High Evidence).","entity_name":"FBXO11","entity_type":"gene"},{"created":"2020-01-22T20:05:08.536896+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FBXO11 as Green List (high evidence)","entity_name":"FBXO11","entity_type":"gene"},{"created":"2020-01-22T20:05:08.524075+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbxo11 has been classified as Green List (High Evidence).","entity_name":"FBXO11","entity_type":"gene"},{"created":"2020-01-22T20:04:11.072147+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.269","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FBXO11 was added\ngene: FBXO11 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: FBXO11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FBXO11 were set to 30057029; 29796876\nPhenotypes for gene: FBXO11 were set to Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, 618089\nReview for gene: FBXO11 was set to GREEN\ngene: FBXO11 was marked as current diagnostic\nAdded comment: Seizures are a feature of ~25% of reported individuals with this condition. \nSources: Expert list","entity_name":"FBXO11","entity_type":"gene"},{"created":"2020-01-22T20:01:00.521180+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FASTKD2 as ready","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T20:01:00.506972+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fastkd2 has been classified as Amber List (Moderate Evidence).","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T20:00:43.849137+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FASTKD2 were changed from  to Mitochondrial complex IV deficiency, MIM#220110","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T20:00:03.266159+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.267","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FASTKD2 were set to ","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T19:59:16.242562+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.266","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FASTKD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T19:58:37.063451+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FASTKD2 as Amber List (moderate evidence)","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T19:58:37.051557+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fastkd2 has been classified as Amber List (Moderate Evidence).","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T19:58:03.020807+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FASTKD2: Rating: AMBER; Mode of pathogenicity: None; Publications: 18771761, 28499982; Phenotypes: Mitochondrial complex IV deficiency, MIM#220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FASTKD2","entity_type":"gene"},{"created":"2020-01-22T18:56:57.620217+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.932","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAR1 as ready","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:56:57.608907+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.932","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:56:44.930844+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAR1 as ready","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:56:44.918947+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:56:25.348498+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.932","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAR1 were set to ","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:56:01.009577+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAR1 were changed from  to Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:55:38.605616+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.931","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAR1 were changed from  to Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:55:27.297039+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAR1 were set to ","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:55:09.519839+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.930","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FAR1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:43.360545+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1662","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FAR1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:42.827187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.929","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAR1 as Amber List (moderate evidence)","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:42.815795+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.929","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:19.452708+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAR1 as ready","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:19.439901+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:54:05.622391+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FAR1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:53:51.501080+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.928","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FAR1: Rating: AMBER; Mode of pathogenicity: None; Publications: 25439727; Phenotypes: Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:53:14.416696+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1660","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAR1 as Amber List (moderate evidence)","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:53:14.403845+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1660","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:52:37.737007+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAR1 were set to ","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:51:54.616805+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1659","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FAR1: Rating: AMBER; Mode of pathogenicity: None; Publications: 25439727; Phenotypes: Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:51:05.562887+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FAR1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:50:37.189540+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.262","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAR1 were changed from  to Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:50:02.083904+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.261","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAR1 as Amber List (moderate evidence)","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:50:02.070777+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.261","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: far1 has been classified as Amber List (Moderate Evidence).","entity_name":"FAR1","entity_type":"gene"},{"created":"2020-01-22T18:49:17.127388+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.260","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FAR1: Rating: AMBER; Mode of pathogenicity: None; Publications: 25439727; Phenotypes: Peroxisomal fatty acyl-CoA reductase 1 disorder, MIM#616154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAR1","entity_type":"gene"}]}