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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1041",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1039",
"results": [
{
"created": "2022-01-18T19:16:10.367905+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc25 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TTC25",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:16:06.450592+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC25 were changed from Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization to Ciliary dyskinesia, primary, 35 (MIM#617092)",
"entity_name": "TTC25",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:15:31.470852+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC25 were set to ",
"entity_name": "TTC25",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:52.135210+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN34 as ready",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:52.125434+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen34 has been classified as Red List (Low Evidence).",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:46.472871+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN34 were changed from PONTOCEREBELLAR HYPOPLASIA TYPE 2 AND TYPE 4 to Pontocerebellar hypoplasia type 2C, MIM# 612390",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:32.229134+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN34 were set to ",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:20.640290+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSEN34 as Red List (low evidence)",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:13:20.631151+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen34 has been classified as Red List (Low Evidence).",
"entity_name": "TSEN34",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:29.834284+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2417",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN2 as ready",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:29.806877+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2417",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen2 has been classified as Green List (High Evidence).",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:24.955649+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2417",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN2 were changed from PONTOCEREBELLAR HYPOPLASIA TYPE 2 AND TYPE 4 to Pontocerebellar hypoplasia type 2B (MIM#612389)",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:13.268948+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN2 were set to ",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:00.563412+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2415",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSEN2 as Green List (high evidence)",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:12:00.553150+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2415",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen2 has been classified as Green List (High Evidence).",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:11:48.075444+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSEN2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pontocerebellar hypoplasia type 2B (MIM#612389); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:10:10.680451+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN15 as ready",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:10:10.667399+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen15 has been classified as Green List (High Evidence).",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:10:04.081321+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN15 were changed from Pontocerebellar Hypoplasia and Progressive Microcephaly to Pontocerebellar hypoplasia, type 2F MIM#617026",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:09:51.392381+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN15 were set to ",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:09:38.460696+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSEN15 as Green List (high evidence)",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:09:38.450589+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen15 has been classified as Green List (High Evidence).",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:08:57.273511+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRMT10A as ready",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:08:57.235418+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10a has been classified as Green List (High Evidence).",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:08:52.849475+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRMT10A as Green List (high evidence)",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:08:52.840466+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10a has been classified as Green List (High Evidence).",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:08:44.749940+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRMT10A was added\ngene: TRMT10A was added to Growth failure. Sources: Expert Review\nMode of inheritance for gene: TRMT10A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TRMT10A were set to 24204302; 25053765; 33448213; 33067246; 26535115; 26526202; 26297882\nPhenotypes for gene: TRMT10A were set to Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; MONDO:0000208\nReview for gene: TRMT10A was set to GREEN\nAdded comment: More than 5 unrelated families reported, short stature is a key feature. \nSources: Expert Review",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:07:29.327357+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRMT10A as ready",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:07:29.316232+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10a has been classified as Green List (High Evidence).",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:07:25.481969+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRMT10A were changed from Microcephaly, short stature, and impaired glucose metabolism 1 to Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; MONDO:0000208",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:55.848643+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRMT10A were set to ",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:45.682579+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRMT10A as Green List (high evidence)",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:45.671595+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10a has been classified as Green List (High Evidence).",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:34.748781+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: More than 5 unrelated families reported. ID is a feature.; to: More than 5 unrelated families reported.",
"entity_name": "TRMT10A",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:04.894751+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIO as ready",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:04.883895+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trio has been classified as Green List (High Evidence).",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:04:01.273431+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIO were changed from INTELLECTUAL DISABILITY to Mental retardation, autosomal dominant 44, MIM# 617061",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:03:47.720522+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIO were set to ",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:03:37.159274+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIO was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:03:27.755899+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIO as Green List (high evidence)",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:03:27.747432+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trio has been classified as Green List (High Evidence).",
"entity_name": "TRIO",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:01:42.871766+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from Bardet-Biedl syndrome 11, MIM# 615988 to Bardet-Biedl syndrome 11, MIM# 615988; Muscular dystrophy, limb-girdle, autosomal recessive 8, MIM# 254110",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:01:26.618471+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Single family reported in 2006.; to: BBS: Single family reported in 2006.\r\n\r\nMuscular dystrophy: onset is typically in childhood.",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:01:08.742815+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TRIM32: Changed phenotypes: Bardet-Biedl syndrome 11, MIM# 615988, Muscular dystrophy, limb-girdle, autosomal recessive 8, MIM# 254110",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:00:25.914862+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:00:25.897683+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:00:21.811894+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from BARDET-BIEDL SYNDROME TYPE 11; LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2H to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:00:06.085918+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2402",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T19:00:06.066258+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2402",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:59:21.454194+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAPPC12 as ready",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:59:21.444318+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:59:07.975311+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Green List (high evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:59:07.958478+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:58:47.346577+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TRAPPC12: Added comment: Agenesis of the corpus callosum and microcephaly.; Changed rating: GREEN",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:58:03.961130+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:57:58.803193+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:57:30.475316+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAPPC11 as ready",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:57:30.465715+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc11 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:57:23.730989+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC11 were changed from MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S to Muscular dystrophy, limb-girdle, autosomal recessive 18 MIM# 615356",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:57:10.647294+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2399",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC11 were set to ",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:56:57.849407+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC11 as Green List (high evidence)",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:56:57.838895+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc11 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:56:44.954908+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRAPPC11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Muscular dystrophy, limb-girdle, autosomal recessive 18 MIM# 615356; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:56:03.705128+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "TRAPPC11",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:55:18.983525+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAIP as ready",
"entity_name": "TRAIP",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:55:18.969738+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traip has been classified as Green List (High Evidence).",
"entity_name": "TRAIP",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:55:15.201558+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAIP were changed from Seckel syndrome 9 to Seckel syndrome 9, MIM#616777",
"entity_name": "TRAIP",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:54:33.683338+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAIP as Green List (high evidence)",
"entity_name": "TRAIP",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:54:33.670944+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traip has been classified as Green List (High Evidence).",
"entity_name": "TRAIP",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:47.930561+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAF3IP1 as ready",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:47.921112+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf3ip1 has been classified as Green List (High Evidence).",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:44.237461+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAF3IP1 were changed from Senior-Loken syndrome 9 to Senior-Loken syndrome 9, MIM# 616629; MONDO:0014712",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:35.719991+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAF3IP1 were set to 26487268; 18364699; 21945076",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:34.321127+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAF3IP1 were set to ",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:21.385823+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAF3IP1 as Green List (high evidence)",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:21.376112+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf3ip1 has been classified as Green List (High Evidence).",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:53:09.156138+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: 5 unrelated families, zebrafish and mouse models.; to: 5 unrelated families, zebrafish and mouse models.\r\n\r\nNephronophthisis is a key feature, polydactyly reported in some.",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:52:11.009050+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOR1A as ready",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:52:10.997532+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1a has been classified as Green List (High Evidence).",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:52:01.860991+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOR1A as Green List (high evidence)",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:52:01.851034+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1a has been classified as Green List (High Evidence).",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:51:27.555172+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOE1 as ready",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:51:27.544683+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: toe1 has been classified as Green List (High Evidence).",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:51:20.392060+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TOE1 were set to ",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:51:06.831343+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOE1 as Green List (high evidence)",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:51:06.820828+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: toe1 has been classified as Green List (High Evidence).",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:50:16.150454+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT3 as ready",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:50:16.140132+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Green List (High Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:50:11.694137+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT3 were set to 25337069; 32779773; 21402185; 17194691; 19142688",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:49:46.596410+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNNT3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:49:35.869131+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2387",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNNT3 as Green List (high evidence)",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:49:35.854745+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2387",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Green List (High Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:47:38.756167+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMX2 as ready",
"entity_name": "TMX2",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:47:38.745314+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmx2 has been classified as Green List (High Evidence).",
"entity_name": "TMX2",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:47:28.151732+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TMX2 as Green List (high evidence)",
"entity_name": "TMX2",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:47:28.105408+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmx2 has been classified as Green List (High Evidence).",
"entity_name": "TMX2",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:30:02.694999+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMTC3 as ready",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:30:02.679209+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmtc3 has been classified as Green List (High Evidence).",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:29:58.328468+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMTC3 were changed from Cobblestone Lissencephaly to Lissencephaly 8 (MIM#617255)",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2022-01-18T18:29:46.397464+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2384",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMTC3 were set to ",
"entity_name": "TMTC3",
"entity_type": "gene"
}
]
}