{"count":220459,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=959","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=957","results":[{"created":"2022-03-01T12:43:10.307328+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Green List (High Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-03-01T12:43:06.069801+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4461","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNORD118 were changed from Leukoencephalopathy with cerebral calcification & cysts to Leukoencephalopathy, brain calcifications, and cysts, MIM# 614561","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-03-01T12:42:50.937077+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4460","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNORD118 were set to ","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-03-01T12:42:17.986725+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Many reported individuals have ID; however overall this is a progressive neurological disorder with variable onset, including in late adulthood.; to: Variable onset, including in infancy with brain abnormalities detectable by imaging.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-03-01T12:41:56.144071+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SNORD118: Changed rating: GREEN","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-03-01T11:16:01.418050+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is not part of the phenotype.; to: Megacolon is a feature.","entity_name":"RET","entity_type":"gene"},{"created":"2022-03-01T11:15:46.136747+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RET: Changed rating: GREEN","entity_name":"RET","entity_type":"gene"},{"created":"2022-03-01T11:13:14.184318+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RFX6 as ready","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:13:14.172074+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rfx6 has been classified as Green List (High Evidence).","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:13:10.427715+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4459","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RFX6 were changed from MARTINEZ-FRIAS SYNDROME to Mitchell-Riley syndrome, MIM#615710","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:12:58.139869+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4458","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RFX6 were set to ","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:12:44.548458+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RFX6: Changed publications: 20148032, 26264437","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:12:27.368653+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is not part of the phenotype.; to: Intestinal atresia.","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:11:53.308599+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RFX6: Changed rating: GREEN","entity_name":"RFX6","entity_type":"gene"},{"created":"2022-03-01T11:11:03.886987+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RIPK4 as ready","entity_name":"RIPK4","entity_type":"gene"},{"created":"2022-03-01T11:11:03.875074+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ripk4 has been classified as Green List (High Evidence).","entity_name":"RIPK4","entity_type":"gene"},{"created":"2022-03-01T11:10:59.675387+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RIPK4 were changed from POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE to Popliteal pterygium syndrome, Bartsocas-Papas type, MIM# 263650","entity_name":"RIPK4","entity_type":"gene"},{"created":"2022-03-01T11:10:37.619741+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4456","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RIPK4 were set to 28425981","entity_name":"RIPK4","entity_type":"gene"},{"created":"2022-03-01T11:09:53.483076+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4455","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RIT1 as ready","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T11:09:53.457537+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4455","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rit1 has been classified as Green List (High Evidence).","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:30:25.190131+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4455","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RIT1 were changed from NOONAN SYNDROME 8 to Noonan syndrome 8, MIM# 615355","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:30:13.419378+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4454","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RIT1 were set to 30712878; 28425981","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:29:58.430898+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4453","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RIT1 was changed from Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:29:56.994582+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4453","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RIT1 was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:29:47.492370+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4452","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RIT1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-03-01T10:29:17.479030+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4451","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2022-03-01T10:29:17.468807+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4451","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2022-03-01T10:29:11.483102+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4451","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMRP were changed from CARTILAGE-HAIR HYPOPLASIA to Anauxetic dysplasia 1, MIM#607095","entity_name":"RMRP","entity_type":"gene"},{"created":"2022-03-01T10:28:57.485683+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Affected individuals are described as having mild ID; note gene is associated with two milder phenotypes, cartilage-hair  hypoplasia and metaphyseal dysplasia without hypotrichosis, which are not associated with ID.; to: Skeletal abnormalities; note gene is associated with two milder phenotypes, cartilage-hair  hypoplasia and metaphyseal dysplasia without hypotrichosis, which are more subtle.","entity_name":"RMRP","entity_type":"gene"},{"created":"2022-03-01T10:28:36.124505+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RMRP: Changed rating: GREEN","entity_name":"RMRP","entity_type":"gene"},{"created":"2022-03-01T10:27:58.105059+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is reported as part of the phenotype. NOTE this gene codes for snRNA, not protein.; to: IUGR. NOTE this gene codes for snRNA, not protein.","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2022-03-01T10:27:46.685280+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNU4ATAC as ready","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2022-03-01T10:27:46.674137+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnu4atac has been classified as Green List (High Evidence).","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2022-03-01T10:27:42.648707+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4450","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNU4ATAC were changed from MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I to Microcephalic osteodysplastic primordial dwarfism, type I, MIM#210710; Roifman syndrome, MIM#616651","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2022-03-01T10:27:29.818074+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4449","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RNU4ATAC was changed from  to Other","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2022-03-01T10:26:58.505649+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4448","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO1 as ready","entity_name":"ROBO1","entity_type":"gene"},{"created":"2022-03-01T10:26:58.494740+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4448","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo1 has been classified as Green List (High Evidence).","entity_name":"ROBO1","entity_type":"gene"},{"created":"2022-03-01T10:26:54.460161+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4448","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ROBO1 were changed from Tetralogy of Fallot and septal defects to Tetralogy of Fallot and septal defects; Congenital heart disease, MONDO:0005453","entity_name":"ROBO1","entity_type":"gene"},{"created":"2022-03-01T10:26:14.664588+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4447","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ROBO1 were changed from tetralogy of Fallot and septal defects to Tetralogy of Fallot and septal defects","entity_name":"ROBO1","entity_type":"gene"},{"created":"2022-03-01T10:26:03.093172+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4446","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ROBO1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ROBO1","entity_type":"gene"},{"created":"2022-03-01T10:24:50.558383+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4445","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROGDI as ready","entity_name":"ROGDI","entity_type":"gene"},{"created":"2022-03-01T10:24:50.545109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4445","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rogdi has been classified as Green List (High Evidence).","entity_name":"ROGDI","entity_type":"gene"},{"created":"2022-03-01T10:24:47.006419+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4445","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ROGDI were changed from KOHLSCHAYTTER-TANZ SYNDROME to Kohlschutter-Tonz syndrome, MIM# 226750","entity_name":"ROGDI","entity_type":"gene"},{"created":"2022-03-01T10:24:32.261068+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4444","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ROGDI were set to ","entity_name":"ROGDI","entity_type":"gene"},{"created":"2022-03-01T10:24:17.864020+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4443","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Kohlschutter-Tonz syndrome (KTZS) is an autosomal recessive disorder characterized by severe global developmental delay, early-onset intractable seizures, spasticity, and amelogenesis imperfecta affecting both primary and secondary teeth and causing yellow or brown discolouration of the teeth. More than 10 families reported.; to: Kohlschutter-Tonz syndrome (KTZS) is an autosomal recessive disorder characterized by severe global developmental delay, early-onset intractable seizures, spasticity, and amelogenesis imperfecta affecting both primary and secondary teeth and causing yellow or brown discolouration of the teeth. More than 10 families reported.\r\n\r\nCerebellar hypoplasia and ventriculomegaly described.","entity_name":"ROGDI","entity_type":"gene"},{"created":"2022-03-01T10:23:12.875010+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4443","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPGRIP1L as ready","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2022-03-01T10:23:12.863885+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4443","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpgrip1l has been classified as Green List (High Evidence).","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2022-03-01T10:23:09.354825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4443","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPGRIP1L were changed from MECKEL SYNDROME TYPE 5; COACH SYNDROME; JOUBERT SYNDROME TYPE 7 to Joubert syndrome 7, MIM# 611560; Meckel syndrome 5, MIM# 611561","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2022-03-01T10:22:56.524792+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4442","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPGRIP1L were set to ","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2022-03-01T10:22:26.461454+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4441","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL11 as ready","entity_name":"RPL11","entity_type":"gene"},{"created":"2022-03-01T10:22:26.447042+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4441","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl11 has been classified as Green List (High Evidence).","entity_name":"RPL11","entity_type":"gene"},{"created":"2022-03-01T10:22:22.608412+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4441","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL11 were changed from Diamond-Blackfan anemia with cleft palate and abnormal thumbs; Diamond-Blackfan anemia 7 612562 to Diamond-Blackfan anemia with cleft palate and abnormal thumbs; Diamond-Blackfan anaemia 7, MIM# 612562; MONDO:0012938","entity_name":"RPL11","entity_type":"gene"},{"created":"2022-03-01T10:22:03.721657+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4440","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL11 were set to ","entity_name":"RPL11","entity_type":"gene"},{"created":"2022-03-01T10:21:52.436727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4439","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL11 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL11","entity_type":"gene"},{"created":"2022-03-01T10:21:21.447680+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4438","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL5 as ready","entity_name":"RPL5","entity_type":"gene"},{"created":"2022-03-01T10:21:21.434918+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4438","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl5 has been classified as Green List (High Evidence).","entity_name":"RPL5","entity_type":"gene"},{"created":"2022-03-01T10:20:50.314804+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4438","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL5 were changed from Diamond-Blackfan anemia 6 612561 to Diamond-Blackfan anaemia 6, MIM# 612561; MONDO:0012937","entity_name":"RPL5","entity_type":"gene"},{"created":"2022-03-01T10:20:35.934817+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4437","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL5 were set to ","entity_name":"RPL5","entity_type":"gene"},{"created":"2022-03-01T10:20:24.993366+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4436","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL5 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL5","entity_type":"gene"},{"created":"2022-03-01T10:19:58.707915+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4435","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS10 as ready","entity_name":"RPS10","entity_type":"gene"},{"created":"2022-03-01T10:19:58.697679+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4435","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps10 has been classified as Green List (High Evidence).","entity_name":"RPS10","entity_type":"gene"},{"created":"2022-03-01T10:19:54.257791+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4435","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS10 were changed from Diamond-Blackfan anemia 9 613308 to Diamond-Blackfan anaemia 9, MIM# 613308","entity_name":"RPS10","entity_type":"gene"},{"created":"2022-03-01T10:19:39.915956+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4434","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS10 were set to ","entity_name":"RPS10","entity_type":"gene"},{"created":"2022-03-01T10:19:02.265182+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4433","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS17 as ready","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-03-01T10:19:02.226846+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps17 has been classified as Green List (High Evidence).","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-03-01T10:18:58.509280+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4433","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4 612527 to Diamond-Blackfan anaemia 4, MIM# 612527","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-03-01T10:18:44.255451+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4432","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS17 were set to ","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-03-01T10:18:32.850841+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4431","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS17 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-03-01T10:18:08.367290+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4430","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS19 as ready","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-03-01T10:18:08.355515+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps19 has been classified as Green List (High Evidence).","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-03-01T10:18:04.796978+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4430","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS19 were changed from RPS19-RELATED DIAMOND-BLACKFAN ANEMIA to Diamond-Blackfan anaemia 1, MIM# 105650; MONDO:0007110","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-03-01T10:17:47.535851+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4429","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS19 were set to ","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-03-01T10:17:32.306779+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4428","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS19 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-03-01T10:16:41.677840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4427","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS26 as ready","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-03-01T10:16:41.667581+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4427","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps26 has been classified as Green List (High Evidence).","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-03-01T10:16:38.055020+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4427","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS26 were changed from Diamond-Blackfan anemia 10 613309 to Diamond-Blackfan anemia 10, MIM# 613309; MONDO:0013217","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-03-01T10:16:26.092206+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4426","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS26 were set to ","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-03-01T10:16:12.252578+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4425","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS26 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-03-01T10:15:09.735424+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4424","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RTTN as ready","entity_name":"RTTN","entity_type":"gene"},{"created":"2022-03-01T10:15:09.724593+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4424","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rttn has been classified as Green List (High Evidence).","entity_name":"RTTN","entity_type":"gene"},{"created":"2022-03-01T10:15:06.201385+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4424","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RTTN were changed from BILATERAL DIFFUSE POLYMICROGYRIA to Microcephaly, short stature, and polymicrogyria with seizures, MIM# 614833; Microcephalic primordial dwarfism due to RTTN deficiency MONDO:0018764","entity_name":"RTTN","entity_type":"gene"},{"created":"2022-03-01T10:14:52.600051+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4423","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RTTN were set to ","entity_name":"RTTN","entity_type":"gene"},{"created":"2022-03-01T10:14:39.098259+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4422","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: More than 10 unrelated families reported, severe microcephaly, ID.; to: More than 10 unrelated families reported, severe microcephaly, PMG.","entity_name":"RTTN","entity_type":"gene"},{"created":"2022-03-01T10:13:19.119853+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4422","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RYR1 as ready","entity_name":"RYR1","entity_type":"gene"},{"created":"2022-03-01T10:13:19.109942+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4422","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ryr1 has been classified as Green List (High Evidence).","entity_name":"RYR1","entity_type":"gene"},{"created":"2022-03-01T10:13:15.540505+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4422","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RYR1 were changed from MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA to Fetal akinesia sequence","entity_name":"RYR1","entity_type":"gene"},{"created":"2022-03-01T10:13:03.058256+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4421","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RYR1 were set to ","entity_name":"RYR1","entity_type":"gene"},{"created":"2022-03-01T10:12:32.718145+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4420","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL1 as ready","entity_name":"SALL1","entity_type":"gene"},{"created":"2022-03-01T10:12:32.706188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4420","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall1 has been classified as Green List (High Evidence).","entity_name":"SALL1","entity_type":"gene"},{"created":"2022-03-01T10:12:28.724247+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4420","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL1 were changed from TOWNES-BROCKS SYNDROME to Townes-Brocks syndrome 1, MIM#107480; MONDO:0054581","entity_name":"SALL1","entity_type":"gene"},{"created":"2022-03-01T10:12:15.199591+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4419","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2022-03-01T10:12:03.399874+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4418","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, limb and other congenital anomalies.","entity_name":"SALL1","entity_type":"gene"},{"created":"2022-03-01T10:11:29.994638+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4418","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL4 as ready","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-01T10:11:29.981247+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4418","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall4 has been classified as Green List (High Evidence).","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-01T10:11:24.147313+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4418","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL4 were changed from ACRO-RENAL-OCULAR SYNDROME; DUANE-RADIAL RAY SYNDROME to Duane-radial ray syndrome, MIM# 607323; MONDO:0011812; IVIC syndrome, MIM# 147750; MONDO:0007836","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-01T10:11:07.265350+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4417","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-01T10:10:34.628055+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4416","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SATB2 as ready","entity_name":"SATB2","entity_type":"gene"},{"created":"2022-03-01T10:10:34.617143+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4416","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: satb2 has been classified as Green List (High Evidence).","entity_name":"SATB2","entity_type":"gene"},{"created":"2022-03-01T10:10:31.059018+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4416","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SATB2 were changed from NONSPECIFIC SEVERE ID; SYNDROMAL PIERRE ROBIN SEQUENCE; CLEFT PALATE ISOLATED to Glass syndrome, MIM# 612313; MONDO:0100147","entity_name":"SATB2","entity_type":"gene"},{"created":"2022-03-01T10:10:17.402023+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4415","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SATB2 were set to ","entity_name":"SATB2","entity_type":"gene"}]}