{"count":220694,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=126","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=124","results":[{"created":"2025-11-20T10:55:29.152472+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.14","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pik3ca has been classified as Red List (Low Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2025-11-20T10:55:25.308433+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.14","user_name":"Chirag Patel","item_type":"entity","text":"gene: XRCC2 was added\ngene: XRCC2 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: XRCC2.\nMode of inheritance for gene: XRCC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: XRCC2 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: XRCC2 was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"XRCC2","entity_type":"gene"},{"created":"2025-11-20T10:55:10.341306+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.13","user_name":"Chirag Patel","item_type":"entity","text":"gene: SLX4 was added\ngene: SLX4 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: SLX4.\nMode of inheritance for gene: SLX4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SLX4 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: SLX4 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"SLX4","entity_type":"gene"},{"created":"2025-11-20T10:54:51.995463+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.12","user_name":"Chirag Patel","item_type":"entity","text":"gene: RINT1 was added\ngene: RINT1 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: RINT1.\nMode of inheritance for gene: RINT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RINT1 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: RINT1 was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"RINT1","entity_type":"gene"},{"created":"2025-11-20T10:54:28.740921+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.11","user_name":"Chirag Patel","item_type":"entity","text":"gene: RAD50 was added\ngene: RAD50 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: RAD50.\nMode of inheritance for gene: RAD50 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RAD50 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: RAD50 was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"RAD50","entity_type":"gene"},{"created":"2025-11-20T10:53:54.566814+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.10","user_name":"Chirag Patel","item_type":"entity","text":"gene: PIK3CA was added\ngene: PIK3CA was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: PIK3CA.\nMode of inheritance for gene: PIK3CA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PIK3CA were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: PIK3CA was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2025-11-20T10:53:50.492255+11:00","panel_name":"Early-onset Dementia","panel_id":24,"panel_version":"1.51","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: SQSTM1 as Amber List (moderate evidence)","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2025-11-20T10:53:50.485563+11:00","panel_name":"Early-onset Dementia","panel_id":24,"panel_version":"1.51","user_name":"Krithika Murali","item_type":"entity","text":"Gene: sqstm1 has been classified as Amber List (Moderate Evidence).","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2025-11-20T10:53:26.879557+11:00","panel_name":"Early-onset Dementia","panel_id":24,"panel_version":"1.51","user_name":"Krithika Murali","item_type":"entity","text":"Classified gene: SQSTM1 as Amber List (moderate evidence)","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2025-11-20T10:53:26.870572+11:00","panel_name":"Early-onset Dementia","panel_id":24,"panel_version":"1.51","user_name":"Krithika Murali","item_type":"entity","text":"Gene: sqstm1 has been classified as Amber List (Moderate Evidence).","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2025-11-20T10:52:24.776742+11:00","panel_name":"Early-onset Dementia","panel_id":24,"panel_version":"1.50","user_name":"Krithika Murali","item_type":"entity","text":"commented on gene: SQSTM1","entity_name":"SQSTM1","entity_type":"gene"},{"created":"2025-11-20T10:51:37.257425+11:00","panel_name":"Dilated Cardiomyopathy","panel_id":95,"panel_version":"1.49","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TMPO as ready","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:51:37.250540+11:00","panel_name":"Dilated Cardiomyopathy","panel_id":95,"panel_version":"1.49","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tmpo has been classified as Red List (Low Evidence).","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:51:34.196401+11:00","panel_name":"Dilated Cardiomyopathy","panel_id":95,"panel_version":"1.49","user_name":"Chirag Patel","item_type":"entity","text":"gene: TMPO was added\ngene: TMPO was added to Dilated Cardiomyopathy. Sources: ClinGen\nrefuted tags were added to gene: TMPO.\nMode of inheritance for gene: TMPO was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: TMPO were set to Dilated cardiomyopathy, MONDO:0005021\nReview for gene: TMPO was set to RED\nAdded comment: ClinGen REFUTED - Nov 2016 \nSources: ClinGen","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:51:28.926928+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.207","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: TMPO.","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:51:22.378021+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.207","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TMPO: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dilated cardiomyopathy, MONDO:0005021; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:50:43.685918+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3582","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: TMPO.","entity_name":"TMPO","entity_type":"gene"},{"created":"2025-11-20T10:47:15.061509+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.275","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SRPX2 as ready","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:47:15.042500+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.275","user_name":"Chirag Patel","item_type":"entity","text":"Gene: srpx2 has been classified as Red List (Low Evidence).","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:46:45.736902+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.275","user_name":"Chirag Patel","item_type":"entity","text":"gene: SRPX2 was added\ngene: SRPX2 was added to Genetic Epilepsy. Sources: ClinGen\nrefuted tags were added to gene: SRPX2.\nMode of inheritance for gene: SRPX2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: SRPX2 were set to Epilepsy, MONDO:0005027\nReview for gene: SRPX2 was set to RED\nAdded comment: ClinGen REFUTED - Oct 2023 \nSources: ClinGen","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:45:41.778618+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.201","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: SRPX2.","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:45:35.868884+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.201","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:45:25.082846+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3582","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:45:13.817166+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3582","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: SRPX2.","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:44:56.910600+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.429","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: SRPX2.","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:44:47.453259+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.429","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SRPX2","entity_type":"gene"},{"created":"2025-11-20T10:43:26.451103+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: SCN9A.","entity_name":"SCN9A","entity_type":"gene"},{"created":"2025-11-20T10:42:21.676574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3582","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene RANGRF from panel Brugada syndrome","entity_name":null,"entity_type":null},{"created":"2025-11-20T10:42:21.054243+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3582","user_name":"Chirag Patel","item_type":"entity","text":"gene: RANGRF was added\ngene: RANGRF was added to Mendeliome. Sources: Expert Review Red,ClinGen\nrefuted tags were added to gene: RANGRF.\nMode of inheritance for gene: RANGRF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RANGRF were set to Brugada syndrome, MONDO:0015263","entity_name":"RANGRF","entity_type":"gene"},{"created":"2025-11-20T10:42:00.281857+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.35","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: RANGRF as ready","entity_name":"RANGRF","entity_type":"gene"},{"created":"2025-11-20T10:42:00.270683+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.35","user_name":"Chirag Patel","item_type":"entity","text":"Gene: rangrf has been classified as Red List (Low Evidence).","entity_name":"RANGRF","entity_type":"gene"},{"created":"2025-11-20T10:41:53.948502+11:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.35","user_name":"Chirag Patel","item_type":"entity","text":"gene: RANGRF was added\ngene: RANGRF was added to Brugada syndrome. Sources: ClinGen\nrefuted tags were added to gene: RANGRF.\nMode of inheritance for gene: RANGRF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RANGRF were set to Brugada syndrome, MONDO:0015263\nReview for gene: RANGRF was set to RED\nAdded comment: ClinGen REFUTED - Oct 2025 \nSources: ClinGen","entity_name":"RANGRF","entity_type":"gene"},{"created":"2025-11-20T10:39:21.221129+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3581","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene RAB40AL from panel Intellectual disability syndromic and non-syndromic","entity_name":null,"entity_type":null},{"created":"2025-11-20T10:39:20.064416+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3581","user_name":"Chirag Patel","item_type":"entity","text":"gene: RAB40AL was added\ngene: RAB40AL was added to Mendeliome. Sources: Expert Review Red,Genetic Health Queensland\nrefuted tags were added to gene: RAB40AL.\nMode of inheritance for gene: RAB40AL was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: RAB40AL were set to 25044830\nPhenotypes for gene: RAB40AL were set to MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE","entity_name":"RAB40AL","entity_type":"gene"},{"created":"2025-11-20T10:38:58.785561+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.429","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: RAB40AL.","entity_name":"RAB40AL","entity_type":"gene"},{"created":"2025-11-20T10:36:21.336002+11:00","panel_name":"Ovarian Cancer","panel_id":4374,"panel_version":"1.3","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MRE11 as ready","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:36:21.328602+11:00","panel_name":"Ovarian Cancer","panel_id":4374,"panel_version":"1.3","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mre11 has been classified as Red List (Low Evidence).","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:36:15.510833+11:00","panel_name":"Ovarian Cancer","panel_id":4374,"panel_version":"1.3","user_name":"Chirag Patel","item_type":"entity","text":"gene: MRE11 was added\ngene: MRE11 was added to Ovarian Cancer. Sources: ClinGen\nrefuted tags were added to gene: MRE11.\nMode of inheritance for gene: MRE11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MRE11 were set to Familial ovarian cancer, MONDO:0016248\nReview for gene: MRE11 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:35:27.607522+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.9","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NBN as ready","entity_name":"NBN","entity_type":"gene"},{"created":"2025-11-20T10:35:27.597844+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.9","user_name":"Chirag Patel","item_type":"entity","text":"Gene: nbn has been classified as Red List (Low Evidence).","entity_name":"NBN","entity_type":"gene"},{"created":"2025-11-20T10:35:23.069196+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.9","user_name":"Chirag Patel","item_type":"entity","text":"gene: NBN was added\ngene: NBN was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: NBN.\nMode of inheritance for gene: NBN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NBN were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: NBN was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"NBN","entity_type":"gene"},{"created":"2025-11-20T10:34:59.695445+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.8","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MUTYH as ready","entity_name":"MUTYH","entity_type":"gene"},{"created":"2025-11-20T10:34:59.685695+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.8","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mutyh has been classified as Red List (Low Evidence).","entity_name":"MUTYH","entity_type":"gene"},{"created":"2025-11-20T10:34:55.411976+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.8","user_name":"Chirag Patel","item_type":"entity","text":"gene: MUTYH was added\ngene: MUTYH was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: MUTYH.\nMode of inheritance for gene: MUTYH was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MUTYH were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: MUTYH was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"MUTYH","entity_type":"gene"},{"created":"2025-11-20T10:34:37.813098+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MSH2 as ready","entity_name":"MSH2","entity_type":"gene"},{"created":"2025-11-20T10:34:37.802865+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: msh2 has been classified as Red List (Low Evidence).","entity_name":"MSH2","entity_type":"gene"},{"created":"2025-11-20T10:34:34.249636+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.7","user_name":"Chirag Patel","item_type":"entity","text":"gene: MSH2 was added\ngene: MSH2 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: MSH2.\nMode of inheritance for gene: MSH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MSH2 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: MSH2 was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"MSH2","entity_type":"gene"},{"created":"2025-11-20T10:34:12.320434+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.6","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MRE11 as ready","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:34:12.310275+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.6","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mre11 has been classified as Red List (Low Evidence).","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:34:09.140940+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.6","user_name":"Chirag Patel","item_type":"entity","text":"gene: MRE11 was added\ngene: MRE11 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: MRE11.\nMode of inheritance for gene: MRE11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MRE11 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: MRE11 was set to RED\nAdded comment: ClinGen REFUTED - Mar 2023 \nSources: ClinGen","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-11-20T10:31:48.376380+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MLH1 as ready","entity_name":"MLH1","entity_type":"gene"},{"created":"2025-11-20T10:31:48.365221+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mlh1 has been classified as Red List (Low Evidence).","entity_name":"MLH1","entity_type":"gene"},{"created":"2025-11-20T10:31:44.612233+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"gene: MLH1 was added\ngene: MLH1 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: MLH1.\nMode of inheritance for gene: MLH1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MLH1 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: MLH1 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"MLH1","entity_type":"gene"},{"created":"2025-11-20T10:30:14.422139+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.291","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MYO1A as ready","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:30:14.414028+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.291","user_name":"Chirag Patel","item_type":"entity","text":"Gene: myo1a has been classified as Red List (Low Evidence).","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:30:08.036272+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.291","user_name":"Chirag Patel","item_type":"entity","text":"gene: MYO1A was added\ngene: MYO1A was added to Deafness_IsolatedAndComplex. Sources: ClinGen\nrefuted tags were added to gene: MYO1A.\nMode of inheritance for gene: MYO1A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1A were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: MYO1A was set to RED\nAdded comment: ClinGen REFUTED - Jan 2018 \nSources: ClinGen","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:29:04.380826+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3580","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: MYO1A as Red List (low evidence)","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:29:04.373783+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3580","user_name":"Chirag Patel","item_type":"entity","text":"Gene: myo1a has been classified as Red List (Low Evidence).","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:28:57.249702+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.30","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: MYO1A as Red List (low evidence)","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:28:57.242934+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.30","user_name":"Chirag Patel","item_type":"entity","text":"Gene: myo1a has been classified as Red List (Low Evidence).","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:28:50.131512+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: MYO1A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital diarrhea, MONDO:0000824; Mode of inheritance: None","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:28:38.238638+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.30","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: MYO1A as Red List (low evidence)","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:28:38.201112+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.30","user_name":"Chirag Patel","item_type":"entity","text":"Gene: myo1a has been classified as Red List (Low Evidence).","entity_name":"MYO1A","entity_type":"gene"},{"created":"2025-11-20T10:26:46.730156+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: MAGI2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MAGI2","entity_type":"gene"},{"created":"2025-11-20T10:26:41.627236+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their review","entity_name":"MAGI2","entity_type":"gene"},{"created":"2025-11-20T10:26:34.701686+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"commented on gene: MAGI2","entity_name":"MAGI2","entity_type":"gene"},{"created":"2025-11-20T10:26:15.641911+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: MAGI2.","entity_name":"MAGI2","entity_type":"gene"},{"created":"2025-11-20T10:25:58.510505+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.152","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: KLF11.","entity_name":"KLF11","entity_type":"gene"},{"created":"2025-11-20T10:25:40.787867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: KLF11.","entity_name":"KLF11","entity_type":"gene"},{"created":"2025-11-20T10:25:19.553697+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.234","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: HARS.","entity_name":"HARS","entity_type":"gene"},{"created":"2025-11-20T10:25:08.846718+11:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: HARS.","entity_name":"HARS","entity_type":"gene"},{"created":"2025-11-20T10:25:00.156461+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.290","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: HARS.","entity_name":"HARS","entity_type":"gene"},{"created":"2025-11-20T10:24:33.205173+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: EPCAM as ready","entity_name":"EPCAM","entity_type":"gene"},{"created":"2025-11-20T10:24:33.195795+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"Gene: epcam has been classified as Red List (Low Evidence).","entity_name":"EPCAM","entity_type":"gene"},{"created":"2025-11-20T10:24:25.511170+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GEN1 as ready","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:24:25.501072+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gen1 has been classified as Red List (Low Evidence).","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:24:15.763484+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GEN1 as ready","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:24:15.754943+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gen1 has been classified as Red List (Low Evidence).","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:21:30.826802+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GEN1 from panel Breast Cancer","entity_name":null,"entity_type":null},{"created":"2025-11-20T10:21:29.664867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3579","user_name":"Chirag Patel","item_type":"entity","text":"gene: GEN1 was added\ngene: GEN1 was added to Mendeliome. Sources: ClinGen\nrefuted tags were added to gene: GEN1.\nMode of inheritance for gene: GEN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GEN1 were set to Hereditary breast carcinoma, MONDO:0016419","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:21:00.356397+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"gene: GEN1 was added\ngene: GEN1 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: GEN1.\nMode of inheritance for gene: GEN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GEN1 were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: GEN1 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"GEN1","entity_type":"gene"},{"created":"2025-11-20T10:20:03.572813+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.470","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: FANCM.","entity_name":"FANCM","entity_type":"gene"},{"created":"2025-11-20T10:19:46.060768+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.83","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: FANCM.","entity_name":"FANCM","entity_type":"gene"},{"created":"2025-11-20T10:18:47.371356+11:00","panel_name":"Colorectal Cancer and Polyposis","panel_id":4371,"panel_version":"1.2","user_name":"Chirag Patel","item_type":"entity","text":"gene: EXO1 was added\ngene: EXO1 was added to Colorectal Cancer and Polyposis. Sources: ClinGen\nrefuted tags were added to gene: EXO1.\nMode of inheritance for gene: EXO1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: EXO1 were set to Lynch syndrome, MONDO:0005835\nReview for gene: EXO1 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"EXO1","entity_type":"gene"},{"created":"2025-11-20T10:17:10.736924+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.3","user_name":"Chirag Patel","item_type":"entity","text":"gene: EPCAM was added\ngene: EPCAM was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: EPCAM.\nMode of inheritance for gene: EPCAM was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: EPCAM were set to Hereditary breast carcinoma, MONDO:0016419\nReview for gene: EPCAM was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"EPCAM","entity_type":"gene"},{"created":"2025-11-20T10:15:35.472372+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"commented on gene: EFHC1","entity_name":"EFHC1","entity_type":"gene"},{"created":"2025-11-20T10:15:09.614469+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"Tag disputed was removed from gene: EFHC1.\nTag refuted tag was added to gene: EFHC1.","entity_name":"EFHC1","entity_type":"gene"},{"created":"2025-11-20T10:13:57.398546+11:00","panel_name":"Ovarian Cancer","panel_id":4374,"panel_version":"1.2","user_name":"Chirag Patel","item_type":"entity","text":"gene: CHEK2 was added\ngene: CHEK2 was added to Ovarian Cancer. Sources: ClinGen\nrefuted tags were added to gene: CHEK2.\nMode of inheritance for gene: CHEK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CHEK2 were set to Familial ovarian cancer, MONDO:0016248\nReview for gene: CHEK2 was set to RED\nAdded comment: ClinGen REFUTED - Apr 2024 \nSources: ClinGen","entity_name":"CHEK2","entity_type":"gene"},{"created":"2025-11-20T10:13:08.624698+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.2","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: BRIP1 as ready","entity_name":"BRIP1","entity_type":"gene"},{"created":"2025-11-20T10:13:08.616502+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.2","user_name":"Chirag Patel","item_type":"entity","text":"Gene: brip1 has been classified as Red List (Low Evidence).","entity_name":"BRIP1","entity_type":"gene"},{"created":"2025-11-20T10:13:03.191585+11:00","panel_name":"Breast Cancer","panel_id":4375,"panel_version":"1.2","user_name":"Chirag Patel","item_type":"entity","text":"gene: BRIP1 was added\ngene: BRIP1 was added to Breast Cancer. Sources: ClinGen\nrefuted tags were added to gene: BRIP1.\nMode of inheritance for gene: BRIP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: BRIP1 were set to Hereditary breast carcinoma  MONDO:0016419\nReview for gene: BRIP1 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen","entity_name":"BRIP1","entity_type":"gene"},{"created":"2025-11-20T10:10:47.107641+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: CHRNA7.","entity_name":"CHRNA7","entity_type":"gene"},{"created":"2025-11-20T10:10:35.306085+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: CHRNA7.","entity_name":"CHRNA7","entity_type":"gene"},{"created":"2025-11-20T10:08:11.605008+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.429","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: CPA6.","entity_name":"CPA6","entity_type":"gene"},{"created":"2025-11-20T10:07:46.119897+11:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"1.39","user_name":"Chirag Patel","item_type":"entity","text":"Tag refuted tag was added to gene: DAO.","entity_name":"DAO","entity_type":"gene"},{"created":"2025-11-20T10:07:28.381215+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CRH as ready","entity_name":"CRH","entity_type":"gene"},{"created":"2025-11-20T10:07:28.369994+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"Gene: crh has been classified as Red List (Low Evidence).","entity_name":"CRH","entity_type":"gene"},{"created":"2025-11-20T10:07:21.240844+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CRH from panel Genetic Epilepsy","entity_name":null,"entity_type":null},{"created":"2025-11-20T10:07:20.167222+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3578","user_name":"Chirag Patel","item_type":"entity","text":"gene: CRH was added\ngene: CRH was added to Mendeliome. Sources: Expert Review Red,ClinGen\nrefuted tags were added to gene: CRH.\nMode of inheritance for gene: CRH was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CRH were set to Epilepsy, MONDO:0005027","entity_name":"CRH","entity_type":"gene"},{"created":"2025-11-20T10:06:59.315197+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.274","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CRH as ready","entity_name":"CRH","entity_type":"gene"}]}