{"count":220751,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=982","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=980","results":[{"created":"2022-02-21T20:39:57.405268+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3786","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PKD1 were changed from Autosomal dominant polycystic kidney disease (ADPKD); Polycystic kidney disease, 173900 to Polycystic kidney disease 1, OMIM #173900","entity_name":"PKD1","entity_type":"gene"},{"created":"2022-02-21T20:39:39.508510+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3785","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PKD1 were set to 23624871; 20558538","entity_name":"PKD1","entity_type":"gene"},{"created":"2022-02-21T20:39:02.176277+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3784","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBL1X as ready","entity_name":"TBL1X","entity_type":"gene"},{"created":"2022-02-21T20:39:02.152614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3784","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbl1x has been classified as Red List (Low Evidence).","entity_name":"TBL1X","entity_type":"gene"},{"created":"2022-02-21T20:38:55.256110+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3784","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TBL1X as Red List (low evidence)","entity_name":"TBL1X","entity_type":"gene"},{"created":"2022-02-21T20:38:55.245051+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3784","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbl1x has been classified as Red List (Low Evidence).","entity_name":"TBL1X","entity_type":"gene"},{"created":"2022-02-21T20:38:42.081202+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3783","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBL1X: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TBL1X","entity_type":"gene"},{"created":"2022-02-21T20:38:08.024565+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3783","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCB1 as ready","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-02-21T20:38:08.013008+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3783","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcb1 has been classified as Green List (High Evidence).","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-02-21T20:38:01.334210+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3783","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCB1 were changed from RHABDOID PREDISPOSITION SYNDROME 1; ?COFFIN-SIRIS SYNDROME to Coffin-Siris syndrome 3, OMIM #614608","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-02-21T20:37:48.408714+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3782","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMARCB1 were set to ","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-02-21T20:37:28.317654+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3781","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMARCB1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-02-21T20:36:37.711896+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3780","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TALDO1 as ready","entity_name":"TALDO1","entity_type":"gene"},{"created":"2022-02-21T20:36:37.699032+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3780","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taldo1 has been classified as Green List (High Evidence).","entity_name":"TALDO1","entity_type":"gene"},{"created":"2022-02-21T20:36:32.879389+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3780","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TALDO1 were set to ","entity_name":"TALDO1","entity_type":"gene"},{"created":"2022-02-21T20:35:52.523398+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3779","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLK4 as ready","entity_name":"PLK4","entity_type":"gene"},{"created":"2022-02-21T20:35:52.514292+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3779","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plk4 has been classified as Green List (High Evidence).","entity_name":"PLK4","entity_type":"gene"},{"created":"2022-02-21T20:35:48.734634+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3779","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLK4 were changed from MICROCEPHALY, GROWTH FAILURE AND RETINOPATHY to Microcephaly and chorioretinopathy, autosomal recessive, 2, OMIM #616171","entity_name":"PLK4","entity_type":"gene"},{"created":"2022-02-21T20:35:34.972694+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3778","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLK4 were set to ","entity_name":"PLK4","entity_type":"gene"},{"created":"2022-02-21T20:35:01.439217+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3777","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUCLG1 as ready","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:35:01.427197+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3777","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: suclg1 has been classified as Green List (High Evidence).","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:34:55.524377+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3777","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUCLG1 were changed from FATAL INFANTILE LACTIC ACIDOSIS to Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MIM#245400","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:34:42.125808+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3776","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUCLG1 were set to 21093335","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:33:35.986669+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SRY as ready","entity_name":"SRY","entity_type":"gene"},{"created":"2022-02-21T20:33:35.973680+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sry has been classified as Green List (High Evidence).","entity_name":"SRY","entity_type":"gene"},{"created":"2022-02-21T20:33:32.201990+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SRY were changed from 46XY SEX REVERSAL 1 to 46XY sex reversal 1, OMIM #400044; 46XX sex reversal 1, OMIM #400045","entity_name":"SRY","entity_type":"gene"},{"created":"2022-02-21T20:33:20.584063+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3774","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SRY were set to ","entity_name":"SRY","entity_type":"gene"},{"created":"2022-02-21T20:32:37.478778+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3773","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TG as ready","entity_name":"TG","entity_type":"gene"},{"created":"2022-02-21T20:32:37.466684+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3773","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tg has been classified as Green List (High Evidence).","entity_name":"TG","entity_type":"gene"},{"created":"2022-02-21T20:32:31.715137+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3773","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TG as Green List (high evidence)","entity_name":"TG","entity_type":"gene"},{"created":"2022-02-21T20:32:31.705317+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3773","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tg has been classified as Green List (High Evidence).","entity_name":"TG","entity_type":"gene"},{"created":"2022-02-21T20:32:02.150196+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC5A5 as ready","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-02-21T20:32:02.138016+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc5a5 has been classified as Green List (High Evidence).","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-02-21T20:31:56.355675+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC5A5 as Green List (high evidence)","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-02-21T20:31:56.344120+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc5a5 has been classified as Green List (High Evidence).","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-02-21T20:31:22.066469+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3771","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRPS1 as ready","entity_name":"TRPS1","entity_type":"gene"},{"created":"2022-02-21T20:31:22.057009+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3771","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trps1 has been classified as Red List (Low Evidence).","entity_name":"TRPS1","entity_type":"gene"},{"created":"2022-02-21T20:31:18.145241+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3771","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRPS1 were changed from TRICHO-RHINO-PHALANGEAL SYNDROME TYPE 1 to Trichorhinophalangeal syndrome, type I, OMIM #190350; Trichorhinophalangeal syndrome, type III, OMIM #190351","entity_name":"TRPS1","entity_type":"gene"},{"created":"2022-02-21T20:31:01.636616+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3770","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRPS1 were set to ","entity_name":"TRPS1","entity_type":"gene"},{"created":"2022-02-21T20:30:43.712220+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3769","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRPS1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRPS1","entity_type":"gene"},{"created":"2022-02-21T20:30:11.192447+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11053","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUCLG1 as ready","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:30:11.182345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11053","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: suclg1 has been classified as Green List (High Evidence).","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:30:03.542680+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11053","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUCLG1 were changed from  to Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MIM#245400","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:29:44.030937+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11052","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUCLG1 were set to ","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:29:20.080467+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11051","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUCLG1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2022-02-21T20:28:48.790982+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3768","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBCE as ready","entity_name":"TBCE","entity_type":"gene"},{"created":"2022-02-21T20:28:48.775830+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3768","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbce has been classified as Green List (High Evidence).","entity_name":"TBCE","entity_type":"gene"},{"created":"2022-02-21T20:28:43.593301+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3768","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBCE were changed from HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy; KENNY-CAFFEY SYNDROME TYPE 1 to Hypoparathyroidism-retardation-dysmorphism syndrome, OMIM #241410; Kenny-Caffey syndrome, type 1, OMIM #244460; Encephalopathy, progressive, with amyotrophy and optic atrophy OMIM #617207","entity_name":"TBCE","entity_type":"gene"},{"created":"2022-02-21T20:28:29.496048+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3767","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBCE were set to ","entity_name":"TBCE","entity_type":"gene"},{"created":"2022-02-21T20:27:51.264506+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3766","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A7 as ready","entity_name":"SLC26A7","entity_type":"gene"},{"created":"2022-02-21T20:27:51.253282+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a7 has been classified as Red List (Low Evidence).","entity_name":"SLC26A7","entity_type":"gene"},{"created":"2022-02-21T20:27:34.320875+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3766","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC26A7 as Red List (low evidence)","entity_name":"SLC26A7","entity_type":"gene"},{"created":"2022-02-21T20:27:34.311511+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a7 has been classified as Red List (Low Evidence).","entity_name":"SLC26A7","entity_type":"gene"},{"created":"2022-02-21T20:27:19.902527+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3765","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC26A7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC26A7","entity_type":"gene"},{"created":"2022-02-21T20:26:45.951417+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11050","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RUNX2 as ready","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:26:45.941798+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11050","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: runx2 has been classified as Green List (High Evidence).","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:26:37.608958+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11050","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RUNX2 were changed from  to Cleidocranial dysplasia MIM#119600; Cleidocranial dysplasia, forme fruste, dental anomalies only MIM#119600; Cleidocranial dysplasia, forme fruste, with brachydactyly MIM#119600; Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly MIM#156510","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:26:23.623854+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11049","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RUNX2 were set to ","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:26:05.309943+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11048","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RUNX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:25:31.234142+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3765","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX7 as ready","entity_name":"PEX7","entity_type":"gene"},{"created":"2022-02-21T20:25:31.222384+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3765","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex7 has been classified as Green List (High Evidence).","entity_name":"PEX7","entity_type":"gene"},{"created":"2022-02-21T20:25:24.637698+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3765","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX7 were changed from RHIZOMELIC CHONDRODYSPLASIA PUNCTATA TYPE 1; REFSUM DISEASE; PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 11 to Peroxisome biogenesis disorder 9B, OMIM# 614879; Rhizomelic chondrodysplasia punctata, type 1, OMIM# 215100","entity_name":"PEX7","entity_type":"gene"},{"created":"2022-02-21T20:25:02.294751+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3764","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX7 were set to ","entity_name":"PEX7","entity_type":"gene"},{"created":"2022-02-21T20:24:11.970205+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3763","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RUNX2 as ready","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:24:11.954102+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3763","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: runx2 has been classified as Green List (High Evidence).","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:24:07.028076+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3763","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RUNX2 were changed from CLEIDOCRANIAL DYSPLASIA to Cleidocranial dysplasia MIM#119600; Cleidocranial dysplasia, forme fruste, with brachydactyly MIM#119600","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:23:54.707345+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3762","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RUNX2 were set to ","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:23:44.696631+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3761","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RUNX2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RUNX2","entity_type":"gene"},{"created":"2022-02-21T20:23:11.176735+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3760","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A4 as ready","entity_name":"SLC26A4","entity_type":"gene"},{"created":"2022-02-21T20:23:11.163396+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a4 has been classified as Red List (Low Evidence).","entity_name":"SLC26A4","entity_type":"gene"},{"created":"2022-02-21T20:23:04.507010+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3760","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC26A4 as Red List (low evidence)","entity_name":"SLC26A4","entity_type":"gene"},{"created":"2022-02-21T20:23:04.485201+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a4 has been classified as Red List (Low Evidence).","entity_name":"SLC26A4","entity_type":"gene"},{"created":"2022-02-21T20:22:52.182059+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3759","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC26A4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC26A4","entity_type":"gene"},{"created":"2022-02-21T20:21:52.384421+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3759","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RTEL1 as ready","entity_name":"RTEL1","entity_type":"gene"},{"created":"2022-02-21T20:21:52.365801+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3759","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rtel1 has been classified as Green List (High Evidence).","entity_name":"RTEL1","entity_type":"gene"},{"created":"2022-02-21T20:21:28.860889+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3759","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RTEL1 were changed from DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4 to Dyskeratosis congenita, autosomal recessive 5 MIM#615190; Hoyeraal-Hreidarsson syndrome","entity_name":"RTEL1","entity_type":"gene"},{"created":"2022-02-21T20:21:05.718356+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3758","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RTEL1 were set to ","entity_name":"RTEL1","entity_type":"gene"},{"created":"2022-02-21T20:20:28.555071+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3757","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROP1 as ready","entity_name":"PROP1","entity_type":"gene"},{"created":"2022-02-21T20:20:28.544093+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3757","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prop1 has been classified as Amber List (Moderate Evidence).","entity_name":"PROP1","entity_type":"gene"},{"created":"2022-02-21T20:20:21.027113+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3757","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PROP1 as Amber List (moderate evidence)","entity_name":"PROP1","entity_type":"gene"},{"created":"2022-02-21T20:20:21.013920+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3757","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prop1 has been classified as Amber List (Moderate Evidence).","entity_name":"PROP1","entity_type":"gene"},{"created":"2022-02-21T20:19:43.235522+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3756","user_name":"Krithika Murali","item_type":"entity","text":"gene: TPO was added\ngene: TPO was added to Fetal anomalies. Sources: Literature\nMode of inheritance for gene: TPO was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TPO were set to 34220711; 30662777\nPhenotypes for gene: TPO were set to Thyroid dyshormonogenesis 2A - MIM#274500\nReview for gene: TPO was set to GREEN\nAdded comment: Well-established association with thyroid dyshormonogenesis.  3 affected individuals from 2 unrelated families reported with  fetal goitre.\r\n\r\n34220711 Rodrigues et al 2021 - report 2 siblings who were diagnosed with fetal goitre on antenatal ultrasound at 26 and 32 weeks gestation. Pathogenic compound het TPO variants identified inherited from unaffected carrier parents.\r\n\r\n30662777 - report a proband diagnosed with fetal goitre at 29 weeks gestation. Compound heterozygous TPO variants identified. \nSources: Literature","entity_name":"TPO","entity_type":"gene"},{"created":"2022-02-21T20:19:16.513076+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11047","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RRM2B as ready","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:19:16.500546+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11047","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rrm2b has been classified as Green List (High Evidence).","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:19:08.032086+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11047","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RRM2B were changed from  to Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy) MIM#612075; Mitochondrial DNA depletion syndrome 8B (MNGIE type) MIM#612075","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:18:48.447171+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11046","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RRM2B were set to ","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:18:30.455049+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11045","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RRM2B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:18:02.457940+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3756","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RRM2B as ready","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:18:02.438243+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3756","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rrm2b has been classified as Red List (Low Evidence).","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:17:58.333132+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3756","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RRM2B were changed from Mitochondrial depletion syndrome to Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy) MIM#612075; Mitochondrial DNA depletion syndrome 8B (MNGIE type) MIM#612075","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:17:45.530735+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3755","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RRM2B were set to ","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:17:35.808206+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3754","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RRM2B as Red List (low evidence)","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:17:35.799371+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3754","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rrm2b has been classified as Red List (Low Evidence).","entity_name":"RRM2B","entity_type":"gene"},{"created":"2022-02-21T20:16:57.094817+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3753","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS6KA3 as ready","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2022-02-21T20:16:57.080961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3753","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps6ka3 has been classified as Green List (High Evidence).","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2022-02-21T20:16:53.261709+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3753","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS6KA3 were changed from COFFIN-LOWRY SYNDROME to Coffin-Lowry syndrome MIM#303600; Intellectual developmental disorder, X-linked 19 MIM#300844","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2022-02-21T20:16:38.747481+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3752","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS6KA3 were set to ","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2022-02-21T20:16:06.952754+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3751","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROR2 as ready","entity_name":"ROR2","entity_type":"gene"},{"created":"2022-02-21T20:16:06.943110+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3751","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ror2 has been classified as Green List (High Evidence).","entity_name":"ROR2","entity_type":"gene"},{"created":"2022-02-21T20:15:58.275160+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3751","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ROR2 were changed from BRACHYDACTYLY, TYPE B1; ROBINOW SYNDROME, AUTOSOMAL DOMINANT; ROR2-RELATED DISORDERS AR to Brachydactyly, type B1 MIM#113000; Robinow syndrome, autosomal recessive MIM#268310","entity_name":"ROR2","entity_type":"gene"}]}