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{
"count": 220842,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1969",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}