{"count":220694,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=122","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=120","results":[{"created":"2025-11-20T17:16:55.284123+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.603","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RYR1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-11-20T17:16:28.040542+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Established gene-disease association, contractures reported.; to: Established gene-disease association, contractures reported, including severe fetal akinesia sequence.","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-11-20T17:16:19.728115+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SCN2B as ready","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:16:19.719131+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Gene: scn2b has been classified as Red List (Low Evidence).","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:16:17.936276+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SCN2B as ready","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:16:17.929679+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Gene: scn2b has been classified as Red List (Low Evidence).","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:16:16.045985+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RYR1: Changed publications: 38520674; Changed phenotypes: Congenital myopathy 1A, autosomal dominant, with susceptibility to malignant hyperthermia, MIM# 117000, Congenital myopathy 1B, autosomal recessive, MIM# 255320; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-11-20T17:15:54.457449+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SLMAP as ready","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:15:54.447041+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"Gene: slmap has been classified as Red List (Low Evidence).","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:15:53.476468+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SCN2B from panel Brugada syndrome","entity_name":null,"entity_type":null},{"created":"2025-11-20T17:15:52.790221+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3622","user_name":"Chirag Patel","item_type":"entity","text":"gene: SCN2B was added\ngene: SCN2B was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: SCN2B.\nMode of inheritance for gene: SCN2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SCN2B were set to Brugada syndrome, MONDO:0015263","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:15:27.665513+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SCN2B as ready","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:15:27.656791+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Gene: scn2b has been classified as Red List (Low Evidence).","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:15:17.107515+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3621","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SLMAP from panel Brugada syndrome","entity_name":null,"entity_type":null},{"created":"2025-11-20T17:15:15.991046+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3621","user_name":"Chirag Patel","item_type":"entity","text":"gene: SLMAP was added\ngene: SLMAP was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: SLMAP.\nMode of inheritance for gene: SLMAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SLMAP were set to Brugada syndrome, MONDO:0015263","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:15:07.963217+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TRPM4 as ready","entity_name":"TRPM4","entity_type":"gene"},{"created":"2025-11-20T17:15:07.955928+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Gene: trpm4 has been classified as Red List (Low Evidence).","entity_name":"TRPM4","entity_type":"gene"},{"created":"2025-11-20T17:14:50.981083+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SLMAP as ready","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:14:50.974108+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Gene: slmap has been classified as Red List (Low Evidence).","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:14:39.186034+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PKP2 as ready","entity_name":"PKP2","entity_type":"gene"},{"created":"2025-11-20T17:14:39.177825+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pkp2 has been classified as Red List (Low Evidence).","entity_name":"PKP2","entity_type":"gene"},{"created":"2025-11-20T17:14:35.553245+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RYR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital myopathy 1A, autosomal dominant, with susceptibility to malignant hyperthermia, MIM# 117000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-11-20T17:13:55.858054+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3620","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: KCNE5.","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:13:53.009311+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: KCNE5 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:13:24.971817+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their comment","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:13:17.241436+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: KCNE5: Added comment: ClinGen DISPUTED - Nov 2017; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:12:31.036444+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMT2 as ready","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:12:31.015015+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomt2 has been classified as Green List (High Evidence).","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:12:28.261589+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POMT2 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, MIM# 613150","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:12:05.012140+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3620","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE5 were changed from Atrial fibrillation to Atrial fibrillation; Brugada syndrome, MONDO:0015263","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:11:56.741023+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.601","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POMT2 were set to ","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:11:35.942830+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3619","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene KCNE5 from panel Brugada syndrome","entity_name":null,"entity_type":null},{"created":"2025-11-20T17:11:28.970057+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.600","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POMT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:10:56.772456+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.599","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POMT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 19138766; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, MIM# 613150; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-11-20T17:10:50.016838+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: KCNE5 as ready","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:10:50.009854+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Gene: kcne5 has been classified as Red List (Low Evidence).","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:10:34.721447+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HCN4 as ready","entity_name":"HCN4","entity_type":"gene"},{"created":"2025-11-20T17:10:34.711314+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hcn4 has been classified as Red List (Low Evidence).","entity_name":"HCN4","entity_type":"gene"},{"created":"2025-11-20T17:10:18.061358+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ANK2 as ready","entity_name":"ANK2","entity_type":"gene"},{"created":"2025-11-20T17:10:18.054461+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ank2 has been classified as Red List (Low Evidence).","entity_name":"ANK2","entity_type":"gene"},{"created":"2025-11-20T17:09:51.578457+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"gene: PKP2 was added\ngene: PKP2 was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: PKP2.\nMode of inheritance for gene: PKP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PKP2 were set to Brugada syndrome, MONDO:0015263\nReview for gene: PKP2 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"PKP2","entity_type":"gene"},{"created":"2025-11-20T17:09:32.549433+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"gene: SLMAP was added\ngene: SLMAP was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: SLMAP.\nMode of inheritance for gene: SLMAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SLMAP were set to Brugada syndrome, MONDO:0015263\nReview for gene: SLMAP was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"SLMAP","entity_type":"gene"},{"created":"2025-11-20T17:09:12.715826+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"gene: SCN2B was added\ngene: SCN2B was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: SCN2B.\nMode of inheritance for gene: SCN2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SCN2B were set to Brugada syndrome, MONDO:0015263\nReview for gene: SCN2B was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"SCN2B","entity_type":"gene"},{"created":"2025-11-20T17:08:58.758312+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"gene: TRPM4 was added\ngene: TRPM4 was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: TRPM4.\nMode of inheritance for gene: TRPM4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: TRPM4 were set to Brugada syndrome, MONDO:0015263\nReview for gene: TRPM4 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"TRPM4","entity_type":"gene"},{"created":"2025-11-20T17:08:40.501537+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.42","user_name":"Chirag Patel","item_type":"entity","text":"gene: KCNE5 was added\ngene: KCNE5 was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: KCNE5.\nMode of inheritance for gene: KCNE5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: KCNE5 were set to Brugada syndrome, MONDO:0015263\nReview for gene: KCNE5 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"KCNE5","entity_type":"gene"},{"created":"2025-11-20T17:08:21.927940+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.42","user_name":"Chirag Patel","item_type":"entity","text":"gene: HCN4 was added\ngene: HCN4 was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: HCN4.\nMode of inheritance for gene: HCN4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HCN4 were set to Brugada syndrome, MONDO:0015263\nReview for gene: HCN4 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"HCN4","entity_type":"gene"},{"created":"2025-11-20T17:08:02.988998+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.42","user_name":"Chirag Patel","item_type":"entity","text":"gene: ANK2 was added\ngene: ANK2 was added to Brugada syndrome. Sources: ClinGen\ndisputed tags were added to gene: ANK2.\nMode of inheritance for gene: ANK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: ANK2 were set to Brugada syndrome, MONDO:0015263\nReview for gene: ANK2 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2017 \nSources: ClinGen","entity_name":"ANK2","entity_type":"gene"},{"created":"2025-11-20T17:06:15.768202+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:06:03.461671+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:05:49.397185+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:05:31.055828+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:05:19.097817+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:05:00.701547+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.41","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:04:48.765285+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.40","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:04:36.716924+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.40","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:04:22.326628+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.40","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNE3 were changed from  to Brugada syndrome, MONDO:0015263","entity_name":"KCNE3","entity_type":"gene"},{"created":"2025-11-20T17:02:56.678499+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.39","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: CACNA2D1 were changed from  to Brugada syndrome 1, MONDO:0011001","entity_name":"CACNA2D1","entity_type":"gene"},{"created":"2025-11-20T17:02:05.782494+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.38","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNJ8 were changed from Brugada syndrome 1, MONDO:0011001 to Brugada syndrome 1, MONDO:0011001","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2025-11-20T17:01:46.865483+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.38","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: KCNJ8 were changed from Brugada syndrome to Brugada syndrome 1, MONDO:0011001","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2025-11-20T17:01:21.629852+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.37","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: SCN1B were changed from Brugada syndrome 1, MONDO:0011001 to Brugada syndrome 1, MONDO:0011001","entity_name":"SCN1B","entity_type":"gene"},{"created":"2025-11-20T17:01:04.205806+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.37","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: SCN1B were changed from  to Brugada syndrome 1, MONDO:0011001","entity_name":"SCN1B","entity_type":"gene"},{"created":"2025-11-20T16:59:17.274340+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3618","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PLAT as ready","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:59:17.261802+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3618","user_name":"Chirag Patel","item_type":"entity","text":"Gene: plat has been classified as Red List (Low Evidence).","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:58:51.865546+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3618","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TP53BP2 as ready","entity_name":"TP53BP2","entity_type":"gene"},{"created":"2025-11-20T16:58:51.858716+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3618","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tp53bp2 has been classified as Red List (Low Evidence).","entity_name":"TP53BP2","entity_type":"gene"},{"created":"2025-11-20T16:58:45.632673+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3618","user_name":"Chirag Patel","item_type":"entity","text":"gene: TP53BP2 was added\ngene: TP53BP2 was added to Mendeliome. Sources: ClinGen\ndisputed tags were added to gene: TP53BP2.\nMode of inheritance for gene: TP53BP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: TP53BP2 were set to Open-angle glaucoma  MONDO:0005338\nReview for gene: TP53BP2 was set to RED\nAdded comment: ClinGen DISPUTED - May 2023 \nSources: ClinGen","entity_name":"TP53BP2","entity_type":"gene"},{"created":"2025-11-20T16:58:20.047103+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3617","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PLAT from panel Bleeding and Platelet Disorders","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:58:19.438295+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3617","user_name":"Chirag Patel","item_type":"entity","text":"gene: PLAT was added\ngene: PLAT was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: PLAT.\nMode of inheritance for gene: PLAT was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PLAT were set to Thrombophilia, familial, due to decreased release of tissue plasminogen activator  MONDO:0012872","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:57:58.420758+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.63","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PLAT as ready","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:57:58.413624+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.63","user_name":"Chirag Patel","item_type":"entity","text":"Gene: plat has been classified as Red List (Low Evidence).","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:57:51.406017+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.63","user_name":"Chirag Patel","item_type":"entity","text":"gene: PLAT was added\ngene: PLAT was added to Bleeding and Platelet Disorders. Sources: ClinGen\ndisputed tags were added to gene: PLAT.\nMode of inheritance for gene: PLAT was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PLAT were set to Thrombophilia, familial, due to decreased release of tissue plasminogen activator  MONDO:0012872\nReview for gene: PLAT was set to RED\nAdded comment: ClinGen DISPUTED - Jun 2023 \nSources: ClinGen","entity_name":"PLAT","entity_type":"gene"},{"created":"2025-11-20T16:56:18.865817+11:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.32","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: MSX1 were changed from Tooth agenesis, selective, 1, MONDO:0007129 to Tooth agenesis, selective, 1, MONDO:0007129","entity_name":"MSX1","entity_type":"gene"},{"created":"2025-11-20T16:55:59.618861+11:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.32","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: MSX1 were changed from Tooth agenesis, selective, 1, MONDO:0007129 to Tooth agenesis, selective, 1, MONDO:0007129","entity_name":"MSX1","entity_type":"gene"},{"created":"2025-11-20T16:55:38.989450+11:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.32","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: MSX1 were changed from  to Tooth agenesis, selective, 1, MONDO:0007129","entity_name":"MSX1","entity_type":"gene"},{"created":"2025-11-20T16:55:03.867562+11:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.31","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: MSX1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Tooth agenesis, selective, 1, MONDO:0007129; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSX1","entity_type":"gene"},{"created":"2025-11-20T16:52:10.534543+11:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.31","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene MSX1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:51:35.787190+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.103","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene MSX1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:51:35.607599+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.282","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene MSX1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:48:54.290736+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3616","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: ACADL were changed from Hereditary pulmonary alveoral proteinosis, MONDO:0012580, ACADL-related to Long chain acyl-CoA dehydrogenase deficiency MONDO:0020531","entity_name":"ACADL","entity_type":"gene"},{"created":"2025-11-20T16:48:47.432203+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3615","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene ACADL from panel Fatty Acid Oxidation Defects","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:48:34.654595+11:00","panel_name":"Fatty Acid Oxidation Defects","panel_id":103,"panel_version":"1.15","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: ACADL were changed from Pulmonary surfactant dysfunction to Long chain acyl-CoA dehydrogenase deficiency MONDO:0020531","entity_name":"ACADL","entity_type":"gene"},{"created":"2025-11-20T16:47:47.119571+11:00","panel_name":"Fatty Acid Oxidation Defects","panel_id":103,"panel_version":"1.14","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: ACADL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Long chain acyl-CoA dehydrogenase deficiency  MONDO:0020531; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACADL","entity_type":"gene"},{"created":"2025-11-20T16:46:56.882070+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.52","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: STEAP3 were changed from Anaemia, hypochromic microcytic, with iron overload 2 MIM# 615234 to Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:46:39.776853+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.38","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: STEAP3 were changed from Anaemia, hypochromic microcytic, with iron overload 2 MIM# 615234 to Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:46:35.952207+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3614","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: STEAP3 were changed from Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094 to Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:46:35.207831+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3614","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: STEAP3 were changed from Anaemia, hypochromic microcytic, with iron overload 2, MIM# 615234 to Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:46:10.369906+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3613","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: STEAP3.","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:46:00.829565+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.37","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene STEAP3 from panel Metal Metabolism Disorders","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:46:00.544273+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3613","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene STEAP3 from panel Metal Metabolism Disorders","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:45:58.596000+11:00","panel_name":"Red cell disorders","panel_id":3366,"panel_version":"1.36","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: STEAP3.","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:45:19.913743+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.51","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: STEAP3.","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:45:14.208777+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.51","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: STEAP3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Severe congenital hypochromic anemia with ringed sideroblasts, MONDO:0014094; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STEAP3","entity_type":"gene"},{"created":"2025-11-20T16:44:25.896817+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3612","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: FOXD3 were changed from Autoimmune disease, susceptibility to, 1 MONDO:0011919 to Autoimmune disease, susceptibility to, 1 MONDO:0011919; Aniridia, MONDO:0019172","entity_name":"FOXD3","entity_type":"gene"},{"created":"2025-11-20T16:43:55.982383+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3611","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their review","entity_name":"FOXD3","entity_type":"gene"},{"created":"2025-11-20T16:43:44.376317+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3611","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene FOXD3 from panel Eye Anterior Segment Abnormalities","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:43:27.207932+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"1.17","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FOXD3 as ready","entity_name":"FOXD3","entity_type":"gene"},{"created":"2025-11-20T16:43:27.199641+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"1.17","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxd3 has been classified as Red List (Low Evidence).","entity_name":"FOXD3","entity_type":"gene"},{"created":"2025-11-20T16:43:21.578515+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"1.17","user_name":"Chirag Patel","item_type":"entity","text":"gene: FOXD3 was added\ngene: FOXD3 was added to Eye Anterior Segment Abnormalities. Sources: ClinGen\ndisputed tags were added to gene: FOXD3.\nMode of inheritance for gene: FOXD3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FOXD3 were set to Aniridia, MONDO:0019172\nReview for gene: FOXD3 was set to RED\nAdded comment: ClinGen DISPUTED - Dec 2022 \nSources: ClinGen","entity_name":"FOXD3","entity_type":"gene"},{"created":"2025-11-20T16:41:14.671192+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3610","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene PRKACG from panel Bleeding and Platelet Disorders","entity_name":null,"entity_type":null},{"created":"2025-11-20T16:41:10.873413+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3609","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed tag was added to gene: PRKACG.","entity_name":"PRKACG","entity_type":"gene"}]}