{"count":220599,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=112","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=110","results":[{"created":"2025-11-27T10:58:08.335717+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.498","user_name":"Chirag Patel","item_type":"entity","text":"gene: NFATC2 was added\ngene: NFATC2 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: NFATC2.\nMode of inheritance for gene: NFATC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NFATC2 were set to Congenital heart disease, MONDO:0005453\nReview for gene: NFATC2 was set to RED\nAdded comment: ClinGen DISPUTED - Mar 2024 \nSources: ClinGen","entity_name":"NFATC2","entity_type":"gene"},{"created":"2025-11-27T10:57:54.088044+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.498","user_name":"Chirag Patel","item_type":"entity","text":"gene: UGDH was added\ngene: UGDH was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: UGDH.\nMode of inheritance for gene: UGDH was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: UGDH were set to Congenital heart disease, MONDO:0005453\nReview for gene: UGDH was set to RED\nAdded comment: ClinGen DISPUTED - Jun 2024 \nSources: ClinGen","entity_name":"UGDH","entity_type":"gene"},{"created":"2025-11-27T10:56:13.161477+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3683","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene RAI2 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:56:12.554468+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3683","user_name":"Chirag Patel","item_type":"entity","text":"gene: RAI2 was added\ngene: RAI2 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: RAI2.\nMode of inheritance for gene: RAI2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RAI2 were set to Congenital heart disease, MONDO:0005453","entity_name":"RAI2","entity_type":"gene"},{"created":"2025-11-27T10:55:55.528412+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3682","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene NFATC1 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:55:53.042424+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.497","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: RAI2 as ready","entity_name":"RAI2","entity_type":"gene"},{"created":"2025-11-27T10:55:53.035619+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.497","user_name":"Chirag Patel","item_type":"entity","text":"Gene: rai2 has been classified as Red List (Low Evidence).","entity_name":"RAI2","entity_type":"gene"},{"created":"2025-11-27T10:55:49.847263+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.497","user_name":"Chirag Patel","item_type":"entity","text":"gene: RAI2 was added\ngene: RAI2 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: RAI2.\nMode of inheritance for gene: RAI2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RAI2 were set to Congenital heart disease, MONDO:0005453\nReview for gene: RAI2 was set to RED\nAdded comment: ClinGen DISPUTED - Apr 2024 \nSources: ClinGen","entity_name":"RAI2","entity_type":"gene"},{"created":"2025-11-27T10:55:38.527170+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.496","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NFATC1 as ready","entity_name":"NFATC1","entity_type":"gene"},{"created":"2025-11-27T10:55:38.519327+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.496","user_name":"Chirag Patel","item_type":"entity","text":"Gene: nfatc1 has been classified as Red List (Low Evidence).","entity_name":"NFATC1","entity_type":"gene"},{"created":"2025-11-27T10:55:01.402141+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.496","user_name":"Chirag Patel","item_type":"entity","text":"gene: NFATC1 was added\ngene: NFATC1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: NFATC1.\nMode of inheritance for gene: NFATC1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NFATC1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: NFATC1 was set to RED\nAdded comment: ClinGen DISPUTED - Jul 2023 \nSources: ClinGen","entity_name":"NFATC1","entity_type":"gene"},{"created":"2025-11-27T10:54:03.089875+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3681","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene CTNNA3 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:53:45.509515+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.495","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CTNNA3 as ready","entity_name":"CTNNA3","entity_type":"gene"},{"created":"2025-11-27T10:53:45.499483+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.495","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ctnna3 has been classified as Red List (Low Evidence).","entity_name":"CTNNA3","entity_type":"gene"},{"created":"2025-11-27T10:53:41.054631+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.495","user_name":"Chirag Patel","item_type":"entity","text":"gene: CTNNA3 was added\ngene: CTNNA3 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: CTNNA3.\nMode of inheritance for gene: CTNNA3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CTNNA3 were set to Congenital heart disease, MONDO:0005453\nReview for gene: CTNNA3 was set to RED\nAdded comment: ClinGen DISPUTED - Oct 2023 \nSources: ClinGen","entity_name":"CTNNA3","entity_type":"gene"},{"created":"2025-11-27T10:51:49.756205+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3680","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NTRK3 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:51:49.106868+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3680","user_name":"Chirag Patel","item_type":"entity","text":"gene: NTRK3 was added\ngene: NTRK3 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: NTRK3.\nMode of inheritance for gene: NTRK3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NTRK3 were set to Congenital heart disease, MONDO:0005453","entity_name":"NTRK3","entity_type":"gene"},{"created":"2025-11-27T10:51:40.436168+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3680","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HEY1 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:51:38.749621+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3680","user_name":"Chirag Patel","item_type":"entity","text":"gene: HEY1 was added\ngene: HEY1 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: HEY1.\nMode of inheritance for gene: HEY1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HEY1 were set to Congenital heart disease, MONDO:0005453","entity_name":"HEY1","entity_type":"gene"},{"created":"2025-11-27T10:51:15.313380+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HEY1 as ready","entity_name":"HEY1","entity_type":"gene"},{"created":"2025-11-27T10:51:15.306479+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hey1 has been classified as Red List (Low Evidence).","entity_name":"HEY1","entity_type":"gene"},{"created":"2025-11-27T10:51:00.423623+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NTRK3 as ready","entity_name":"NTRK3","entity_type":"gene"},{"created":"2025-11-27T10:51:00.415285+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ntrk3 has been classified as Red List (Low Evidence).","entity_name":"NTRK3","entity_type":"gene"},{"created":"2025-11-27T10:50:24.621683+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"gene: NTRK3 was added\ngene: NTRK3 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: NTRK3.\nMode of inheritance for gene: NTRK3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NTRK3 were set to Congenital heart disease, MONDO:0005453\nReview for gene: NTRK3 was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2024 \nSources: ClinGen","entity_name":"NTRK3","entity_type":"gene"},{"created":"2025-11-27T10:50:07.505757+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.494","user_name":"Chirag Patel","item_type":"entity","text":"gene: HEY1 was added\ngene: HEY1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: HEY1.\nMode of inheritance for gene: HEY1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HEY1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: HEY1 was set to RED\nAdded comment: ClinGen DISPUTED - Aug 2024 \nSources: ClinGen","entity_name":"HEY1","entity_type":"gene"},{"created":"2025-11-27T10:48:56.025133+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.493","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: OSR1 as ready","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:48:56.017985+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.493","user_name":"Chirag Patel","item_type":"entity","text":"Gene: osr1 has been classified as Red List (Low Evidence).","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:48:51.567299+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3679","user_name":"Chirag Patel","item_type":"entity","text":"changed review comment from: ClinGen DISPUTED - Aug 2024; to: ClinGen DISPUTED - Apr 2024","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:48:51.438196+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.493","user_name":"Chirag Patel","item_type":"entity","text":"gene: OSR1 was added\ngene: OSR1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: OSR1.\nMode of inheritance for gene: OSR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: OSR1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: OSR1 was set to RED\nAdded comment: ClinGen DISPUTED - Apr 2024 \nSources: ClinGen","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:47:48.487279+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3679","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: OSR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:47:33.642212+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3679","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: OSR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:47:31.963885+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3679","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: OSR1 were changed from  to Congenital heart disease, MONDO:0005453","entity_name":"OSR1","entity_type":"gene"},{"created":"2025-11-27T10:46:48.978425+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3678","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene LEFTY2 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:46:31.750880+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.492","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: LEFTY2 as ready","entity_name":"LEFTY2","entity_type":"gene"},{"created":"2025-11-27T10:46:31.743156+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.492","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lefty2 has been classified as Red List (Low Evidence).","entity_name":"LEFTY2","entity_type":"gene"},{"created":"2025-11-27T10:46:27.048206+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.492","user_name":"Chirag Patel","item_type":"entity","text":"gene: LEFTY2 was added\ngene: LEFTY2 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: LEFTY2.\nMode of inheritance for gene: LEFTY2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: LEFTY2 were set to Congenital heart disease, MONDO:0005453\nReview for gene: LEFTY2 was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2024 \nSources: ClinGen","entity_name":"LEFTY2","entity_type":"gene"},{"created":"2025-11-27T10:45:38.740909+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3677","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CSRP1 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:45:38.097282+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3677","user_name":"Chirag Patel","item_type":"entity","text":"gene: CSRP1 was added\ngene: CSRP1 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: CSRP1.\nMode of inheritance for gene: CSRP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CSRP1 were set to Congenital heart disease, MONDO:0005453","entity_name":"CSRP1","entity_type":"gene"},{"created":"2025-11-27T10:45:27.546433+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3677","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ATE1 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:45:25.040387+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3677","user_name":"Chirag Patel","item_type":"entity","text":"gene: ATE1 was added\ngene: ATE1 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: ATE1.\nMode of inheritance for gene: ATE1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATE1 were set to Congenital heart disease, MONDO:0005453","entity_name":"ATE1","entity_type":"gene"},{"created":"2025-11-27T10:45:18.657323+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.491","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CSRP1 as ready","entity_name":"CSRP1","entity_type":"gene"},{"created":"2025-11-27T10:45:18.645804+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.491","user_name":"Chirag Patel","item_type":"entity","text":"Gene: csrp1 has been classified as Red List (Low Evidence).","entity_name":"CSRP1","entity_type":"gene"},{"created":"2025-11-27T10:45:15.488633+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.491","user_name":"Chirag Patel","item_type":"entity","text":"gene: CSRP1 was added\ngene: CSRP1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: CSRP1.\nMode of inheritance for gene: CSRP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CSRP1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: CSRP1 was set to RED\nAdded comment: ClinGen DISPUTED - Jul 2024 \nSources: ClinGen","entity_name":"CSRP1","entity_type":"gene"},{"created":"2025-11-27T10:45:06.013505+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.490","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ATE1 as ready","entity_name":"ATE1","entity_type":"gene"},{"created":"2025-11-27T10:45:05.998086+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.490","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ate1 has been classified as Red List (Low Evidence).","entity_name":"ATE1","entity_type":"gene"},{"created":"2025-11-27T10:44:44.223865+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.490","user_name":"Chirag Patel","item_type":"entity","text":"gene: ATE1 was added\ngene: ATE1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: ATE1.\nMode of inheritance for gene: ATE1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATE1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: ATE1 was set to RED\nAdded comment: ClinGen DISPUTED - Aug 2023 \nSources: ClinGen","entity_name":"ATE1","entity_type":"gene"},{"created":"2025-11-27T10:43:23.536753+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.489","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: DCHS1 as ready","entity_name":"DCHS1","entity_type":"gene"},{"created":"2025-11-27T10:43:23.529801+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.489","user_name":"Chirag Patel","item_type":"entity","text":"Gene: dchs1 has been classified as Red List (Low Evidence).","entity_name":"DCHS1","entity_type":"gene"},{"created":"2025-11-27T10:43:11.732183+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3676","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: FOXL1 were changed from Otosclerosis 11 #MIM620576 to Otosclerosis 11 #MIM620576; Congenital heart disease, MONDO:0005453","entity_name":"FOXL1","entity_type":"gene"},{"created":"2025-11-27T10:42:55.865080+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.489","user_name":"Chirag Patel","item_type":"entity","text":"gene: DCHS1 was added\ngene: DCHS1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: DCHS1.\nMode of inheritance for gene: DCHS1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DCHS1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: DCHS1 was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2024 \nSources: ClinGen","entity_name":"DCHS1","entity_type":"gene"},{"created":"2025-11-27T10:41:52.688453+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3675","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene FOXL1 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:41:33.844584+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.488","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FOXL1 as ready","entity_name":"FOXL1","entity_type":"gene"},{"created":"2025-11-27T10:41:33.833679+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.488","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxl1 has been classified as Red List (Low Evidence).","entity_name":"FOXL1","entity_type":"gene"},{"created":"2025-11-27T10:41:24.066504+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.488","user_name":"Chirag Patel","item_type":"entity","text":"gene: FOXL1 was added\ngene: FOXL1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: FOXL1.\nMode of inheritance for gene: FOXL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FOXL1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: FOXL1 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2023 \nSources: ClinGen","entity_name":"FOXL1","entity_type":"gene"},{"created":"2025-11-27T10:40:36.210047+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3674","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FMO5 from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:40:34.946832+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3674","user_name":"Chirag Patel","item_type":"entity","text":"gene: FMO5 was added\ngene: FMO5 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: FMO5.\nMode of inheritance for gene: FMO5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FMO5 were set to Congenital heart disease, MONDO:0005453","entity_name":"FMO5","entity_type":"gene"},{"created":"2025-11-27T10:40:14.676624+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.487","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FMO5 as ready","entity_name":"FMO5","entity_type":"gene"},{"created":"2025-11-27T10:40:14.668897+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.487","user_name":"Chirag Patel","item_type":"entity","text":"Gene: fmo5 has been classified as Red List (Low Evidence).","entity_name":"FMO5","entity_type":"gene"},{"created":"2025-11-27T10:40:00.211886+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.487","user_name":"Chirag Patel","item_type":"entity","text":"gene: FMO5 was added\ngene: FMO5 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: FMO5.\nMode of inheritance for gene: FMO5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FMO5 were set to Congenital heart disease, MONDO:0005453\nReview for gene: FMO5 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2023 \nSources: ClinGen","entity_name":"FMO5","entity_type":"gene"},{"created":"2025-11-27T10:39:52.513130+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.486","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: DTNA as ready","entity_name":"DTNA","entity_type":"gene"},{"created":"2025-11-27T10:39:52.501908+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.486","user_name":"Chirag Patel","item_type":"entity","text":"Gene: dtna has been classified as Red List (Low Evidence).","entity_name":"DTNA","entity_type":"gene"},{"created":"2025-11-27T10:39:06.662305+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3673","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene DTNA from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:36:26.937933+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3672","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene DTNA from panel Congenital Heart Defect","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:35:42.115833+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.486","user_name":"Chirag Patel","item_type":"entity","text":"gene: DTNA was added\ngene: DTNA was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: DTNA.\nMode of inheritance for gene: DTNA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DTNA were set to Congenital heart disease, MONDO:0005453\nReview for gene: DTNA was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2024 \nSources: ClinGen","entity_name":"DTNA","entity_type":"gene"},{"created":"2025-11-27T10:32:16.015685+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.485","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: FOXP1 as Red List (low evidence)","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:32:15.999784+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.485","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxp1 has been classified as Red List (Low Evidence).","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:31:58.444759+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.485","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: FOXP1 as Red List (low evidence)","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:31:58.428529+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.485","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxp1 has been classified as Red List (Low Evidence).","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:31:37.385515+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.484","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: FOXP1.","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:31:30.658354+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.484","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FOXP1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: congenital heart disease, MONDO:0005453; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-11-27T10:19:26.943809+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.286","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: ZDHHC15.","entity_name":"ZDHHC15","entity_type":"gene"},{"created":"2025-11-27T10:18:17.429048+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.573","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: LAMC3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:18:04.224044+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.573","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: LAMC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:17:51.184800+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.572","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:17:30.998506+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.572","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:17:13.123990+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.571","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:16:59.849692+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.571","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from  to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:16:30.207528+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their comment","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:16:25.935383+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: LAMC3: Added comment: Occipital cortical malformations not corpus callosum; Changed phenotypes: Cortical malformations, occipital, MIM#614115; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:15:59.868471+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: LAMC3 as Red List (low evidence)","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:15:59.837163+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lamc3 has been classified as Red List (Low Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:15:57.099468+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: LAMC3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:15:46.194567+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: LAMC3 as Red List (low evidence)","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:15:46.184437+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.570","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lamc3 has been classified as Red List (Low Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:14:20.808275+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.230","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: MET were changed from ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278 to complex neurodevelopmental disorder, MONDO:0100038","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:13:47.841546+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.229","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: MET.","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:13:42.162003+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.229","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: MET: Added comment: ClinGen DISPUTED - Jan 2021; Changed phenotypes: complex neurodevelopmental disorder, MONDO:0100038; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:13:11.686274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.455","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: LAMC3 as Green List (high evidence)","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:13:11.674040+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.455","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lamc3 has been classified as Green List (High Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:12:58.110746+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.455","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: LAMC3 as Green List (high evidence)","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:12:58.100993+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.455","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lamc3 has been classified as Green List (High Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2025-11-27T10:11:38.346447+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.454","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: MET were changed from ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278 to complex neurodevelopmental disorder, MONDO:0100038","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:11:24.419084+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.454","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: MET was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:10:58.630724+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.453","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: MET.","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:10:51.707779+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.453","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: MET: Added comment: ClinGen DISPUTED - Jan 2021; Changed phenotypes: complex neurodevelopmental disorder, MONDO:0100038; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MET","entity_type":"gene"},{"created":"2025-11-27T10:08:14.698252+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.229","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: RELN.","entity_name":"RELN","entity_type":"gene"},{"created":"2025-11-27T10:08:14.068805+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.453","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene FAAH2 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:06:36.533786+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3671","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: CLIC2.","entity_name":"CLIC2","entity_type":"gene"},{"created":"2025-11-27T10:05:23.855104+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3671","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene EN2 from panel Intellectual disability syndromic and non-syndromic","entity_name":null,"entity_type":null},{"created":"2025-11-27T10:05:22.708837+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3671","user_name":"Chirag Patel","item_type":"entity","text":"gene: EN2 was added\ngene: EN2 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: EN2.\nMode of inheritance for gene: EN2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: EN2 were set to Complex neurodevelopmental disorder,  MONDO:0100038","entity_name":"EN2","entity_type":"gene"}]}