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{
"count": 220694,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=126",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}