{"count":221416,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=439","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=437","results":[{"created":"2024-06-04T23:29:30.874657+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPFIA3 were set to 38723631","entity_name":"PPFIA3","entity_type":"gene"},{"created":"2024-06-04T23:28:13.463591+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPFIA3 were set to 37034625","entity_name":"PPFIA3","entity_type":"gene"},{"created":"2024-06-04T23:27:12.194266+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PPFIA3: Changed publications: 38723631","entity_name":"PPFIA3","entity_type":"gene"},{"created":"2024-06-04T22:57:11.429684+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1806","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRRC23 were changed from Non-syndromic male infertility due to sperm motility disorder,  (MONDO:0017173), LRRC23-related to Spermatogenic failure 92, MIM# 620848","entity_name":"LRRC23","entity_type":"gene"},{"created":"2024-06-04T22:56:43.781916+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1805","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRRC23 were set to 37804054","entity_name":"LRRC23","entity_type":"gene"},{"created":"2024-06-04T22:56:17.720426+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1804","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LRRC23 as Amber List (moderate evidence)","entity_name":"LRRC23","entity_type":"gene"},{"created":"2024-06-04T22:56:17.698589+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1804","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrrc23 has been classified as Amber List (Moderate Evidence).","entity_name":"LRRC23","entity_type":"gene"},{"created":"2024-06-04T22:55:53.667870+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1803","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LRRC23: Rating: AMBER; Mode of pathogenicity: None; Publications: 38091523; Phenotypes: Spermatogenic failure 92, MIM# 620848; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LRRC23","entity_type":"gene"},{"created":"2024-06-03T17:26:38.490751+10:00","panel_name":"Aminoacidopathy","panel_id":3929,"panel_version":"1.47","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"gene: GCSH was added\ngene: GCSH was added to Aminoacidopathy. Sources: ClinGen\nMode of inheritance for gene: GCSH was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GCSH were set to 33890291; 36190515; 33569080\nPhenotypes for gene: GCSH were set to glycine encephalopathy MONDO:0011612\nReview for gene: GCSH was set to GREEN\nAdded comment: Classified Strong by ClinGen Aminoacidopathy GCEP on 10/02/2023 - https://search.clinicalgenome.org/CCID:004937\r\n\r\nReported in 7 individuals with abnormal biochemical metabolism. \nSources: ClinGen","entity_name":"GCSH","entity_type":"gene"},{"created":"2024-06-03T16:53:23.672967+10:00","panel_name":"Aminoacidopathy","panel_id":3929,"panel_version":"1.47","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"edited their review of gene: GCDH: Changed rating: GREEN","entity_name":"GCDH","entity_type":"gene"},{"created":"2024-06-03T16:53:14.074854+10:00","panel_name":"Aminoacidopathy","panel_id":3929,"panel_version":"1.47","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"gene: GCH1 was added\ngene: GCH1 was added to Aminoacidopathy. Sources: ClinGen\nMode of inheritance for gene: GCH1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GCH1 were set to 20301681, 9749603, 10582612, 11026444, 15303002\nPhenotypes for gene: GCH1 were set to GTP cyclohydrolase I deficiency MONDO:0100184\nReview for gene: GCH1 was set to GREEN\nAdded comment: Classified Definitive by ClinGen Aminoacidopathy GCEP on 11/12/2020 - https://search.clinicalgenome.org/CCID:004935\r\n\r\nAD individuals have less than 50% GTPCH activity suggesting a dominant negative mechanism of disease. \r\n\r\nAR individuals are shown to have severe deficiency of GTPCH activity resulting in hhyperphenylalaninemia due to secondary PAH deficiency which can be detected on NBS. \nSources: ClinGen","entity_name":"GCH1","entity_type":"gene"},{"created":"2024-06-03T16:21:06.466565+10:00","panel_name":"Aminoacidopathy","panel_id":3929,"panel_version":"1.47","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"gene: GCDH was added\ngene: GCDH was added to Aminoacidopathy. Sources: ClinGen\nMode of inheritance for gene: GCDH was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GCDH were set to 31536184, 7795610, 27476540, 31062211\nPhenotypes for gene: GCDH were set to glutaryl-CoA dehydrogenase deficiency MONDO:0009281\nAdded comment: Classified Definitive by ClinGen Aminoacidopathy GCEP on 08/11/2019 - https://search.clinicalgenome.org/CCID:004934\r\n\r\nWell established gene-disease association. \r\nAffected individuals present with abnormal glutaric acid, 3-hydroxy-glutaric acid, glutaconic acid and glutarylcarnitine.\r\nc.91+5G>T has been reported to segregate closely within closely related Native American kindreds. \nSources: ClinGen","entity_name":"GCDH","entity_type":"gene"},{"created":"2024-06-02T23:21:40.381299+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLD1 were changed from Combined immunodeficiency, MONDO:0015131, POLD1-related; Low CD4 T cells; Low B cells, normal maturation; recurrent respiratory tract infections, skin infections, warts and molluscum; short stature; intellectual disability to Immunodeficiency 120, MIM# 620836; Low CD4 T cells; Low B cells, normal maturation; recurrent respiratory tract infections, skin infections, warts and molluscum; short stature; intellectual disability","entity_name":"POLD1","entity_type":"gene"},{"created":"2024-06-02T23:20:58.496825+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.64","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: POLD1: Changed phenotypes: Immunodeficiency 120, MIM# 620836, Low CD4 T cells, Low B cells, normal maturation, recurrent respiratory tract infections, skin infections, warts and molluscum, short stature, intellectual disability","entity_name":"POLD1","entity_type":"gene"},{"created":"2024-06-02T23:20:25.089125+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1803","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLD1 were changed from Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, MIM# 615381; MONDO:0014157; Combined immunodeficiency, MONDO:0015131, POLD1-related to Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, MIM# 615381; MONDO:0014157; Immunodeficiency 120, MIM#\t620836","entity_name":"POLD1","entity_type":"gene"},{"created":"2024-06-02T23:19:46.056831+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1802","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: POLD1: Changed phenotypes: Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, MIM# 615381, MONDO:0014157, Immunodeficiency 120, MIM# 620836","entity_name":"POLD1","entity_type":"gene"},{"created":"2024-06-02T23:18:09.669013+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.64","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ICOSLG were changed from Combined immunodeficiency; recurrent bacterial and viral infections; neutropaenia to Immunodeficiency 119, MIM# 620825; Combined immunodeficiency; recurrent bacterial and viral infections; neutropaenia","entity_name":"ICOSLG","entity_type":"gene"},{"created":"2024-06-02T23:17:31.245433+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ICOSLG: Changed phenotypes: Immunodeficiency 119, MIM# 620825, Combined immunodeficiency, recurrent bacterial and viral infections, neutropaenia","entity_name":"ICOSLG","entity_type":"gene"},{"created":"2024-06-02T23:17:02.586269+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1802","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ICOSLG were changed from Combined immunodeficiency; recurrent bacterial and viral infections; neutropaenia to Immunodeficiency 119, MIM# 620825; Combined immunodeficiency; recurrent bacterial and viral infections; neutropaenia","entity_name":"ICOSLG","entity_type":"gene"},{"created":"2024-06-02T23:16:32.256939+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1801","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ICOSLG: Changed phenotypes: Immunodeficiency 119, MIM#  620825, Combined immunodeficiency, recurrent bacterial and viral infections, neutropaenia","entity_name":"ICOSLG","entity_type":"gene"},{"created":"2024-05-30T14:22:35.565811+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.326","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYCP2L were changed from Premature ovarian insufficiency to Premature ovarian failure 24, MIM# 620840","entity_name":"SYCP2L","entity_type":"gene"},{"created":"2024-05-30T14:22:07.881531+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1801","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYCP2L were changed from Premature ovarian insufficiency to Premature ovarian failure 24, MIM#\t620840","entity_name":"SYCP2L","entity_type":"gene"},{"created":"2024-05-30T14:05:04.903906+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.275","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG4 as ready","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:05:04.887825+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.275","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:05:00.877163+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.275","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Red List (low evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:05:00.860101+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.275","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:04:11.413530+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.274","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Red List (low evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:04:11.389613+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.274","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2024-05-30T14:03:19.896207+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.273","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCC as ready","entity_name":"DCC","entity_type":"gene"},{"created":"2024-05-30T14:03:19.881637+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.273","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcc has been classified as Red List (Low Evidence).","entity_name":"DCC","entity_type":"gene"},{"created":"2024-05-30T14:03:07.907601+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.273","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCC as Red List (low evidence)","entity_name":"DCC","entity_type":"gene"},{"created":"2024-05-30T14:03:07.890336+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.273","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcc has been classified as Red List (Low Evidence).","entity_name":"DCC","entity_type":"gene"},{"created":"2024-05-30T14:02:20.513885+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.272","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CUL3 as ready","entity_name":"CUL3","entity_type":"gene"},{"created":"2024-05-30T14:02:20.501095+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cul3 has been classified as Red List (Low Evidence).","entity_name":"CUL3","entity_type":"gene"},{"created":"2024-05-30T14:02:15.340104+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.272","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CUL3 as Red List (low evidence)","entity_name":"CUL3","entity_type":"gene"},{"created":"2024-05-30T14:02:15.319860+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cul3 has been classified as Red List (Low Evidence).","entity_name":"CUL3","entity_type":"gene"},{"created":"2024-05-30T14:00:00.955908+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.271","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNMT3A as ready","entity_name":"DNMT3A","entity_type":"gene"},{"created":"2024-05-30T14:00:00.938018+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.271","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnmt3a has been classified as Red List (Low Evidence).","entity_name":"DNMT3A","entity_type":"gene"},{"created":"2024-05-30T13:59:55.272366+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.271","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNMT3A as Red List (low evidence)","entity_name":"DNMT3A","entity_type":"gene"},{"created":"2024-05-30T13:59:55.258061+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.271","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnmt3a has been classified as Red List (Low Evidence).","entity_name":"DNMT3A","entity_type":"gene"},{"created":"2024-05-30T13:58:22.532306+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.270","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EHMT1 as ready","entity_name":"EHMT1","entity_type":"gene"},{"created":"2024-05-30T13:58:22.518948+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.270","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ehmt1 has been classified as Red List (Low Evidence).","entity_name":"EHMT1","entity_type":"gene"},{"created":"2024-05-30T13:58:08.639134+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.270","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EHMT1 as Red List (low evidence)","entity_name":"EHMT1","entity_type":"gene"},{"created":"2024-05-30T13:58:08.626034+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.270","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ehmt1 has been classified as Red List (Low Evidence).","entity_name":"EHMT1","entity_type":"gene"},{"created":"2024-05-30T13:57:14.595914+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.269","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EZH2 as ready","entity_name":"EZH2","entity_type":"gene"},{"created":"2024-05-30T13:57:14.564224+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.269","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ezh2 has been classified as Red List (Low Evidence).","entity_name":"EZH2","entity_type":"gene"},{"created":"2024-05-30T13:57:05.986596+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.269","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EZH2 as Red List (low evidence)","entity_name":"EZH2","entity_type":"gene"},{"created":"2024-05-30T13:57:05.972938+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.269","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ezh2 has been classified as Red List (Low Evidence).","entity_name":"EZH2","entity_type":"gene"},{"created":"2024-05-30T13:56:19.567751+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.268","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR1 as ready","entity_name":"FGFR1","entity_type":"gene"},{"created":"2024-05-30T13:56:19.554673+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.268","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr1 has been classified as Red List (Low Evidence).","entity_name":"FGFR1","entity_type":"gene"},{"created":"2024-05-30T13:56:14.703909+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.268","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGFR1 as Red List (low evidence)","entity_name":"FGFR1","entity_type":"gene"},{"created":"2024-05-30T13:56:14.689217+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.268","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr1 has been classified as Red List (Low Evidence).","entity_name":"FGFR1","entity_type":"gene"},{"created":"2024-05-30T13:55:20.922728+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.267","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FUS as ready","entity_name":"FUS","entity_type":"gene"},{"created":"2024-05-30T13:55:20.907273+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.267","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fus has been classified as Red List (Low Evidence).","entity_name":"FUS","entity_type":"gene"},{"created":"2024-05-30T13:55:15.298414+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.267","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FUS as Red List (low evidence)","entity_name":"FUS","entity_type":"gene"},{"created":"2024-05-30T13:55:15.281410+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.267","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fus has been classified as Red List (Low Evidence).","entity_name":"FUS","entity_type":"gene"},{"created":"2024-05-30T13:54:27.955429+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABBR2 as ready","entity_name":"GABBR2","entity_type":"gene"},{"created":"2024-05-30T13:54:27.936834+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabbr2 has been classified as Red List (Low Evidence).","entity_name":"GABBR2","entity_type":"gene"},{"created":"2024-05-30T13:54:21.949714+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GABBR2 as Red List (low evidence)","entity_name":"GABBR2","entity_type":"gene"},{"created":"2024-05-30T13:54:21.927915+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabbr2 has been classified as Red List (Low Evidence).","entity_name":"GABBR2","entity_type":"gene"},{"created":"2024-05-30T13:53:09.132737+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.265","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATAD2B as ready","entity_name":"GATAD2B","entity_type":"gene"},{"created":"2024-05-30T13:53:09.115465+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gatad2b has been classified as Red List (Low Evidence).","entity_name":"GATAD2B","entity_type":"gene"},{"created":"2024-05-30T13:53:05.198959+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.265","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATAD2B as Red List (low evidence)","entity_name":"GATAD2B","entity_type":"gene"},{"created":"2024-05-30T13:53:05.184630+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gatad2b has been classified as Red List (Low Evidence).","entity_name":"GATAD2B","entity_type":"gene"},{"created":"2024-05-30T13:51:57.662782+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.264","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRIN2A as ready","entity_name":"GRIN2A","entity_type":"gene"},{"created":"2024-05-30T13:51:57.640415+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.264","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grin2a has been classified as Red List (Low Evidence).","entity_name":"GRIN2A","entity_type":"gene"},{"created":"2024-05-30T13:51:53.808157+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.264","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GRIN2A as Red List (low evidence)","entity_name":"GRIN2A","entity_type":"gene"},{"created":"2024-05-30T13:51:53.795743+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.264","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grin2a has been classified as Red List (Low Evidence).","entity_name":"GRIN2A","entity_type":"gene"},{"created":"2024-05-30T13:51:04.243886+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.263","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HIVEP2 as ready","entity_name":"HIVEP2","entity_type":"gene"},{"created":"2024-05-30T13:51:04.229336+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hivep2 has been classified as Red List (Low Evidence).","entity_name":"HIVEP2","entity_type":"gene"},{"created":"2024-05-30T13:50:55.886973+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.263","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HIVEP2 as Red List (low evidence)","entity_name":"HIVEP2","entity_type":"gene"},{"created":"2024-05-30T13:50:55.873830+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hivep2 has been classified as Red List (Low Evidence).","entity_name":"HIVEP2","entity_type":"gene"},{"created":"2024-05-30T13:50:02.976581+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.262","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KAT6B as ready","entity_name":"KAT6B","entity_type":"gene"},{"created":"2024-05-30T13:50:02.959472+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.262","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat6b has been classified as Red List (Low Evidence).","entity_name":"KAT6B","entity_type":"gene"},{"created":"2024-05-30T13:49:52.161568+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.262","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KAT6B as Red List (low evidence)","entity_name":"KAT6B","entity_type":"gene"},{"created":"2024-05-30T13:49:52.132622+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.262","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat6b has been classified as Red List (Low Evidence).","entity_name":"KAT6B","entity_type":"gene"},{"created":"2024-05-30T13:49:04.797439+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.261","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNH1 as ready","entity_name":"KCNH1","entity_type":"gene"},{"created":"2024-05-30T13:49:04.778579+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.261","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnh1 has been classified as Red List (Low Evidence).","entity_name":"KCNH1","entity_type":"gene"},{"created":"2024-05-30T13:48:58.207541+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.261","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNH1 as Red List (low evidence)","entity_name":"KCNH1","entity_type":"gene"},{"created":"2024-05-30T13:48:58.193040+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.261","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnh1 has been classified as Red List (Low Evidence).","entity_name":"KCNH1","entity_type":"gene"},{"created":"2024-05-30T13:46:57.653204+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.260","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNQ3 as ready","entity_name":"KCNQ3","entity_type":"gene"},{"created":"2024-05-30T13:46:57.633746+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.260","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnq3 has been classified as Red List (Low Evidence).","entity_name":"KCNQ3","entity_type":"gene"},{"created":"2024-05-30T13:46:51.486756+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.260","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNQ3 as Red List (low evidence)","entity_name":"KCNQ3","entity_type":"gene"},{"created":"2024-05-30T13:46:51.471368+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.260","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnq3 has been classified as Red List (Low Evidence).","entity_name":"KCNQ3","entity_type":"gene"},{"created":"2024-05-30T13:45:52.623834+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.259","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNQ5 as ready","entity_name":"KCNQ5","entity_type":"gene"},{"created":"2024-05-30T13:45:52.601556+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.259","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnq5 has been classified as Red List (Low Evidence).","entity_name":"KCNQ5","entity_type":"gene"},{"created":"2024-05-30T13:45:34.476541+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.259","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNQ5 as Red List (low evidence)","entity_name":"KCNQ5","entity_type":"gene"},{"created":"2024-05-30T13:45:34.461306+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.259","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnq5 has been classified as Red List (Low Evidence).","entity_name":"KCNQ5","entity_type":"gene"},{"created":"2024-05-30T13:44:36.065606+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.258","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KMT2D as ready","entity_name":"KMT2D","entity_type":"gene"},{"created":"2024-05-30T13:44:36.047922+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.258","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kmt2d has been classified as Red List (Low Evidence).","entity_name":"KMT2D","entity_type":"gene"},{"created":"2024-05-30T13:44:14.770303+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.258","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KMT2D as Red List (low evidence)","entity_name":"KMT2D","entity_type":"gene"},{"created":"2024-05-30T13:44:14.757639+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.258","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kmt2d has been classified as Red List (Low Evidence).","entity_name":"KMT2D","entity_type":"gene"},{"created":"2024-05-30T13:43:11.772239+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.257","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MACF1 as ready","entity_name":"MACF1","entity_type":"gene"},{"created":"2024-05-30T13:43:11.758850+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.257","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Red List (Low Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2024-05-30T13:43:06.601132+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.257","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MACF1 as Red List (low evidence)","entity_name":"MACF1","entity_type":"gene"},{"created":"2024-05-30T13:43:06.584044+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.257","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Red List (Low Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2024-05-30T13:42:17.441819+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.256","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MBD5 as ready","entity_name":"MBD5","entity_type":"gene"},{"created":"2024-05-30T13:42:17.401199+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.256","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mbd5 has been classified as Red List (Low Evidence).","entity_name":"MBD5","entity_type":"gene"},{"created":"2024-05-30T13:42:12.373884+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.256","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MBD5 as Red List (low evidence)","entity_name":"MBD5","entity_type":"gene"},{"created":"2024-05-30T13:42:12.358510+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.256","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mbd5 has been classified as Red List (Low Evidence).","entity_name":"MBD5","entity_type":"gene"}]}