{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1041","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}