{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=302","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=300","results":[{"created":"2025-01-24T11:08:45.906750+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1329","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM138 were set to ","entity_name":"TMEM138","entity_type":"gene"},{"created":"2025-01-24T11:08:17.960970+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1328","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR19 as ready","entity_name":"WDR19","entity_type":"gene"},{"created":"2025-01-24T11:08:17.940543+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1328","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr19 has been classified as Green List (High Evidence).","entity_name":"WDR19","entity_type":"gene"},{"created":"2025-01-24T11:08:14.383971+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1328","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR19 were changed from Senior-Loken syndrome 8, 616307 (3) to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378","entity_name":"WDR19","entity_type":"gene"},{"created":"2025-01-24T11:07:44.496868+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1327","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR19 were set to ","entity_name":"WDR19","entity_type":"gene"},{"created":"2025-01-24T11:07:17.032373+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1326","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL4A5 as ready","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-01-24T11:07:17.018048+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1326","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a5 has been classified as Green List (High Evidence).","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-01-24T11:07:09.130906+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1326","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL4A5 were changed from Alport syndrome 1, X-linked to Alport syndrome 1, X-linked, MIM#301050","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-01-24T11:06:56.871859+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1325","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL4A5 were set to ","entity_name":"COL4A5","entity_type":"gene"},{"created":"2025-01-24T11:06:22.397717+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1324","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM126A as ready","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-01-24T11:06:22.363065+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1324","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem126a has been classified as Green List (High Evidence).","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-01-24T11:06:18.793790+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1324","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM126A were changed from Optic atrophy 7, 612989 (3) to Optic atrophy 7 MIM#612989","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-01-24T11:06:05.456719+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1323","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM126A were set to ","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-01-24T11:05:34.295869+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1322","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM67 as ready","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-01-24T11:05:34.279553+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1322","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem67 has been classified as Green List (High Evidence).","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-01-24T11:05:30.801277+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1322","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM67 were changed from Joubert syndrome 6, 610688 (3) to COACH syndrome 1 MIM#216360; Joubert syndrome 6 MIM#610688; Meckel syndrome 3 MIM#607361; Nephronophthisis 11 MIM#613550","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-01-24T11:05:18.386638+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1321","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM67 were set to ","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-01-24T11:04:49.248323+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1320","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFRSF11A as ready","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-01-24T11:04:49.236375+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1320","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf11a has been classified as Green List (High Evidence).","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-01-24T11:04:44.919116+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1320","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNFRSF11A were changed from Osteopetrosis, autosomal recessive 7, 612301 (3) to Osteopetrosis, autosomal recessive 7, MIM#612301","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-01-24T11:04:32.818519+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1319","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFRSF11A were set to ","entity_name":"TNFRSF11A","entity_type":"gene"},{"created":"2025-01-24T11:04:05.064224+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TP53RK as ready","entity_name":"TP53RK","entity_type":"gene"},{"created":"2025-01-24T11:04:05.020465+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tp53rk has been classified as Red List (Low Evidence).","entity_name":"TP53RK","entity_type":"gene"},{"created":"2025-01-24T11:03:58.292443+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: TP53RK.","entity_name":"TP53RK","entity_type":"gene"},{"created":"2025-01-24T11:03:18.934359+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC19 as ready","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-01-24T11:03:18.921059+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc19 has been classified as Green List (High Evidence).","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-01-24T11:03:15.985920+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1318","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC19 were changed from Mitochondrial complex III deficiency, nuclear type 2, 615157 (3) to Mitochondrial complex III deficiency, nuclear type 2 MIM#615157","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-01-24T11:03:02.862095+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1317","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC19 were set to ","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-01-24T11:02:34.912432+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1316","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPE65 as ready","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-01-24T11:02:34.900285+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1316","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpe65 has been classified as Green List (High Evidence).","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-01-24T11:02:31.340912+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1316","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPE65 were changed from Leber congenital amaurosis 2, 204100 (3) to Retinitis pigmentosa 20, MIM#613794; Leber congenital amaurosis 2, MIM#204100","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-01-24T11:01:41.222500+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1315","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TYRP1 as ready","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-01-24T11:01:41.201125+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1315","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyrp1 has been classified as Green List (High Evidence).","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-01-24T11:01:30.891904+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1315","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TYRP1 were set to ","entity_name":"TYRP1","entity_type":"gene"},{"created":"2025-01-23T19:10:07.635952+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.295","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR1 were changed from neurodevelopmental disorder MONDO:0700092, FLVCR1-related to Neurodevelopmental disorder with microcephaly, absent speech, and hypotonia, MIM#621060","entity_name":"FLVCR1","entity_type":"gene"},{"created":"2025-01-23T19:09:27.688723+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.294","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLVCR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, absent speech, and hypotonia, MIM#621060; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR1","entity_type":"gene"},{"created":"2025-01-23T19:09:05.126949+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2270","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR1 were changed from posterior column ataxia-retinitis pigmentosa syndrome MONDO:0012177; neurodevelopmental disorder MONDO:0700092, FLVCR1-related to posterior column ataxia-retinitis pigmentosa syndrome MONDO:0012177; Neurodevelopmental disorder with microcephaly, absent speech, and hypotonia, MIM#621060","entity_name":"FLVCR1","entity_type":"gene"},{"created":"2025-01-23T19:06:06.912585+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2269","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLVCR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, absent speech, and hypotonia, MIM#621060; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR1","entity_type":"gene"},{"created":"2025-01-23T18:45:22.782057+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1314","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POMP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Keratosis linearis with ichthyosis congenita and sclerosing keratoderma MIM#601952; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"POMP","entity_type":"gene"},{"created":"2025-01-23T16:50:24.835420+11:00","panel_name":"Cardiac conduction disease","panel_id":4422,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added Panel Cardiac conduction disease\nSet list of related panels to Cardiac conduction abnormality; HP:0031546\nSet panel types to: Victorian Clinical Genetics Services; Royal Melbourne Hospital","entity_name":null,"entity_type":null},{"created":"2025-01-23T15:55:31.971024+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1314","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS6KA3 as ready","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-01-23T15:55:31.957510+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1314","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":"2025-01-23T15:55:25.809635+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1314","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":"2025-01-23T15:54:40.134413+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1313","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS6KA3 were set to ","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-01-23T14:31:08.263307+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1312","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USB1 as ready","entity_name":"USB1","entity_type":"gene"},{"created":"2025-01-23T14:31:08.250878+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1312","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: usb1 has been classified as Green List (High Evidence).","entity_name":"USB1","entity_type":"gene"},{"created":"2025-01-23T14:30:53.854431+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1312","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USB1 were changed from Poikiloderma with neutropenia, 604173 (3) to Poikiloderma with neutropenia MIM#604173","entity_name":"USB1","entity_type":"gene"},{"created":"2025-01-23T14:28:58.901671+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1311","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USB1 were set to ","entity_name":"USB1","entity_type":"gene"},{"created":"2025-01-23T14:28:15.621466+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1310","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HESX1 as ready","entity_name":"HESX1","entity_type":"gene"},{"created":"2025-01-23T14:28:15.611571+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1310","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hesx1 has been classified as Green List (High Evidence).","entity_name":"HESX1","entity_type":"gene"},{"created":"2025-01-23T14:28:11.995437+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1310","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HESX1 were changed from Septooptic dysplasia, 182230 (3) to Septooptic dysplasia, MIM#182230; Pituitary hormone deficiency, combined, 5 MIM#182230; Growth hormone deficiency with pituitary anomalies, MIM#182230","entity_name":"HESX1","entity_type":"gene"},{"created":"2025-01-23T14:28:00.451761+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1309","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HESX1 were set to ","entity_name":"HESX1","entity_type":"gene"},{"created":"2025-01-23T14:27:33.023905+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1308","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VMA21 as ready","entity_name":"VMA21","entity_type":"gene"},{"created":"2025-01-23T14:27:33.012052+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1308","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vma21 has been classified as Green List (High Evidence).","entity_name":"VMA21","entity_type":"gene"},{"created":"2025-01-23T14:27:29.310396+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1308","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VMA21 were changed from Myopathy, X-linked, with excessive autophagy, 310440 (3), X-linked recessive to Myopathy, X-linked, with excessive autophagy MIM#310440","entity_name":"VMA21","entity_type":"gene"},{"created":"2025-01-23T14:27:14.423299+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1307","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VMA21 were set to ","entity_name":"VMA21","entity_type":"gene"},{"created":"2025-01-23T14:26:37.146960+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1306","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GHR as ready","entity_name":"GHR","entity_type":"gene"},{"created":"2025-01-23T14:26:37.134721+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1306","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ghr has been classified as Green List (High Evidence).","entity_name":"GHR","entity_type":"gene"},{"created":"2025-01-23T14:26:32.607469+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1306","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GHR were changed from Laron dwarfism, 262500 (3) to Laron dwarfism, MIM#262500","entity_name":"GHR","entity_type":"gene"},{"created":"2025-01-23T14:26:20.148102+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1305","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GHR were set to ","entity_name":"GHR","entity_type":"gene"},{"created":"2025-01-23T14:25:49.198726+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1304","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WARS2 as ready","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-01-23T14:25:49.187018+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1304","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wars2 has been classified as Green List (High Evidence).","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-01-23T14:25:45.457373+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1304","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WARS2 were changed from Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, 617710 (3), Autosomal recessive to Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures MIM#617710; Parkinsonism-dystonia 3, childhood-onset MIM#619738","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-01-23T14:25:30.051069+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1303","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WARS2 were set to ","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-01-23T14:25:03.223031+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1302","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTS as ready","entity_name":"PTS","entity_type":"gene"},{"created":"2025-01-23T14:25:03.208097+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1302","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pts has been classified as Green List (High Evidence).","entity_name":"PTS","entity_type":"gene"},{"created":"2025-01-23T14:24:57.028551+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1302","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTS were changed from Hyperphenylalaninemia, BH4-deficient, A, 261640 (3) to Hyperphenylalaninemia, BH4-deficient, A, MIM# 261640","entity_name":"PTS","entity_type":"gene"},{"created":"2025-01-23T14:24:44.081381+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1301","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PTS were set to ","entity_name":"PTS","entity_type":"gene"},{"created":"2025-01-23T14:24:16.590662+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1300","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHDDS as ready","entity_name":"DHDDS","entity_type":"gene"},{"created":"2025-01-23T14:24:16.568470+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1300","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhdds has been classified as Green List (High Evidence).","entity_name":"DHDDS","entity_type":"gene"},{"created":"2025-01-23T14:24:13.120133+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1300","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHDDS were changed from Retinitis pigmentosa 59, 613861 (3) to Retinitis pigmentosa 59, MIM#613861; Congenital disorder of glycosylation, type 1bb, MIM# 613861","entity_name":"DHDDS","entity_type":"gene"},{"created":"2025-01-23T14:24:00.723127+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1299","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHDDS were set to ","entity_name":"DHDDS","entity_type":"gene"},{"created":"2025-01-23T14:23:30.901135+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1298","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WFS1 as ready","entity_name":"WFS1","entity_type":"gene"},{"created":"2025-01-23T14:23:30.887271+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1298","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wfs1 has been classified as Green List (High Evidence).","entity_name":"WFS1","entity_type":"gene"},{"created":"2025-01-23T14:23:25.333818+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1298","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WFS1 were changed from Wolfram syndrome, 222300 (3) to Wolfram syndrome 1 MIM#222300","entity_name":"WFS1","entity_type":"gene"},{"created":"2025-01-23T14:23:12.923391+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1297","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WFS1 were set to ","entity_name":"WFS1","entity_type":"gene"},{"created":"2025-01-23T14:22:42.743787+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1296","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RETREG1 as ready","entity_name":"RETREG1","entity_type":"gene"},{"created":"2025-01-23T14:22:42.728573+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1296","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: retreg1 has been classified as Green List (High Evidence).","entity_name":"RETREG1","entity_type":"gene"},{"created":"2025-01-23T14:22:34.526586+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1296","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RETREG1 were changed from Neuropathy, hereditary sensory and autonomic, type IIB, 613115 (3) to Neuropathy, hereditary sensory and autonomic, type IIB, MIM# 613115; MONDO:0013142","entity_name":"RETREG1","entity_type":"gene"},{"created":"2025-01-23T14:22:18.268052+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1295","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RETREG1 were set to ","entity_name":"RETREG1","entity_type":"gene"},{"created":"2025-01-23T14:20:57.590417+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1294","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLNA as ready","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-01-23T14:20:57.574673+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1294","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flna has been classified as Green List (High Evidence).","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-01-23T14:20:50.872394+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1294","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLNA were changed from FG syndrome 2, 300321 (3) to FG syndrome 2, MIM#300321; Frontometaphyseal dysplasia 1, MIM#305620; Heterotopia, periventricular, 1, MIM#300049; Intestinal pseudoobstruction, neuronal, MIM#300048; Melnick-Needles syndrome, MIM#309350; Otopalatodigital syndrome, type I, MIM#311300; Otopalatodigital syndrome, type II, MIM#304120; Terminal osseous dysplasia, MIM#300244","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-01-23T14:19:34.917031+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1293","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLNA were set to ","entity_name":"FLNA","entity_type":"gene"},{"created":"2025-01-23T14:15:46.638132+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1292","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLA1 as ready","entity_name":"POLA1","entity_type":"gene"},{"created":"2025-01-23T14:15:46.616739+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1292","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pola1 has been classified as Amber List (Moderate Evidence).","entity_name":"POLA1","entity_type":"gene"},{"created":"2025-01-23T14:15:42.079589+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1292","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POLA1 were set to ","entity_name":"POLA1","entity_type":"gene"},{"created":"2025-01-23T14:15:27.491542+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1291","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: POLA1.","entity_name":"POLA1","entity_type":"gene"},{"created":"2025-01-23T14:13:15.847749+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1291","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOK7 as ready","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-01-23T14:13:15.831877+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1291","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dok7 has been classified as Green List (High Evidence).","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-01-23T14:13:12.909370+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1291","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOK7 were changed from Myasthenic syndrome, congenital, 10, 254300 (3) to Myasthenic syndrome, congenital, 10, MIM# 254300; Fetal akinesia deformation sequence 3, MIM# 618389","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-01-23T14:12:58.800127+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1290","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DOK7 were set to ","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-01-23T14:12:31.213786+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1289","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDA as ready","entity_name":"EDA","entity_type":"gene"},{"created":"2025-01-23T14:12:31.203162+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1289","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eda has been classified as Green List (High Evidence).","entity_name":"EDA","entity_type":"gene"},{"created":"2025-01-23T14:12:25.934573+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1289","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EDA were changed from Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3) to Ectodermal dysplasia 1, hypohidrotic, X-linked MIM#305100","entity_name":"EDA","entity_type":"gene"},{"created":"2025-01-23T14:12:11.774726+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1288","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EDA were set to ","entity_name":"EDA","entity_type":"gene"},{"created":"2025-01-23T14:02:06.006171+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1287","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPG5 as ready","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-01-23T14:02:05.989801+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1287","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epg5 has been classified as Green List (High Evidence).","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-01-23T14:01:59.732667+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1287","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPG5 were changed from Vici syndrome, 242840 (3) to Vici syndrome MIM# 242840","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-01-23T14:01:43.260551+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1286","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPG5 were set to ","entity_name":"EPG5","entity_type":"gene"}]}