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{
"count": 220694,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=125",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=123",
"results": [
{
"created": "2025-11-20T12:31:49.325948+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: SEMA4A as ready",
"entity_name": "SEMA4A",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:31:49.318640+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: sema4a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA4A",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:31:46.482094+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SEMA4A was added\ngene: SEMA4A was added to Colorectal Cancer and Polyposis. Sources: ClinGen\ndisputed tags were added to gene: SEMA4A.\nMode of inheritance for gene: SEMA4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SEMA4A were set to Lynch syndrome, MONDO:0005835\nReview for gene: SEMA4A was set to RED\nAdded comment: ClinGen DISPUTED - Mar 2024 \nSources: ClinGen",
"entity_name": "SEMA4A",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:30:59.572286+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "edited their review of gene: MUTYH: Added comment: ClinGen DISPUTED (AD) - Mar 2023; Changed rating: RED; Changed phenotypes: Colorectal cancer, MONDO:0005575; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:29:44.861795+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: BARD1 as ready",
"entity_name": "BARD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:29:44.851101+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: bard1 has been classified as Red List (Low Evidence).",
"entity_name": "BARD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:29:37.932206+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: BARD1 was added\ngene: BARD1 was added to Ovarian Cancer. Sources: ClinGen\ndisputed tags were added to gene: BARD1.\nMode of inheritance for gene: BARD1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: BARD1 were set to Familial ovarian cancer, MONDO:0016248\nReview for gene: BARD1 was set to RED\nAdded comment: ClinGen DISPUTED - Aug 2024 \nSources: ClinGen",
"entity_name": "BARD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:28:38.370778+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MUTYH as ready",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:28:38.363730+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.5",
"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": "2025-11-20T12:28:34.737828+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MUTYH was added\ngene: MUTYH was added to Ovarian Cancer. Sources: ClinGen\ndisputed tags were added to gene: MUTYH.\nMode of inheritance for gene: MUTYH was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: MUTYH were set to Familial ovarian cancer, MONDO:0016248\nReview for gene: MUTYH was set to RED\nAdded comment: ClinGen DISPUTED (AR and AD) - Dec 2023 \nSources: ClinGen",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:28:08.864401+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: MUTYH was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:26:26.479156+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MUTYH.",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:26:19.721775+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:26:15.299992+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "edited their review of gene: MUTYH: Added comment: ClinGen DISPUTED (AR) and REFUTED (AD) - Dec 2023; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:21:58.830502+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3590",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MYO1F as ready",
"entity_name": "MYO1F",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:21:58.820460+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3590",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: myo1f has been classified as Red List (Low Evidence).",
"entity_name": "MYO1F",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:21:45.900492+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3590",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYO1F was added\ngene: MYO1F was added to Mendeliome. Sources: ClinGen\ndisputed tags were added to gene: MYO1F.\nMode of inheritance for gene: MYO1F was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1F were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: MYO1F was set to RED\nAdded comment: ClinGen DISPUTED - Oct 2024 \nSources: ClinGen",
"entity_name": "MYO1F",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:20:01.306298+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3589",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CEMIP as ready",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:20:01.289652+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3589",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cemip has been classified as Red List (Low Evidence).",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:19:49.146900+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3589",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CEMIP from panel Deafness_IsolatedAndComplex",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T12:19:48.030395+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3589",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CEMIP was added\ngene: CEMIP was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: CEMIP.\nMode of inheritance for gene: CEMIP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEMIP were set to Nonsyndromic genetic hearing loss, MONDO:0019497",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:19:25.169867+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CEMIP as ready",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:19:25.160433+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cemip has been classified as Red List (Low Evidence).",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:18:50.582290+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3588",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MYO1C as ready",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:18:50.561026+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3588",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: myo1c has been classified as Red List (Low Evidence).",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:17:56.366544+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: GJA1 as ready",
"entity_name": "GJA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:17:56.356488+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: gja1 has been classified as Red List (Low Evidence).",
"entity_name": "GJA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:17:38.529610+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3588",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene MYO1C from panel Deafness_IsolatedAndComplex",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T12:17:37.959476+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3588",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYO1C was added\ngene: MYO1C was added to Mendeliome. Sources: ClinGen\ndisputed tags were added to gene: MYO1C.\nMode of inheritance for gene: MYO1C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1C were set to Nonsyndromic genetic hearing loss, MONDO:0019497",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:17:31.572393+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MYO1C as ready",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:17:31.559091+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: myo1c has been classified as Red List (Low Evidence).",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:16:27.496289+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.294",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYO1F was added\ngene: MYO1F was added to Deafness_IsolatedAndComplex. Sources: ClinGen\ndisputed tags were added to gene: MYO1F.\nMode of inheritance for gene: MYO1F was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1F were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: MYO1F was set to RED\nAdded comment: ClinGen DISPUTED - Oct 2024 \nSources: ClinGen",
"entity_name": "MYO1F",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:16:09.964431+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.293",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYO1F was added\ngene: MYO1F was added to Deafness_IsolatedAndComplex. Sources: ClinGen\ndisputed tags were added to gene: MYO1F.\nMode of inheritance for gene: MYO1F was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1F were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: MYO1F was set to RED\nAdded comment: ClinGen DISPUTED - Oct 2024 \nSources: ClinGen",
"entity_name": "MYO1F",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:15:52.559257+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.293",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYO1C was added\ngene: MYO1C was added to Deafness_IsolatedAndComplex. Sources: ClinGen\ndisputed tags were added to gene: MYO1C.\nMode of inheritance for gene: MYO1C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYO1C were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: MYO1C was set to RED\nAdded comment: ClinGen DISPUTED - Jun 2018 \nSources: ClinGen",
"entity_name": "MYO1C",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:15:32.417848+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.292",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: GJA1 was added\ngene: GJA1 was added to Deafness_IsolatedAndComplex. Sources: ClinGen\ndisputed tags were added to gene: GJA1.\nMode of inheritance for gene: GJA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GJA1 were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: GJA1 was set to RED\nAdded comment: ClinGen DISPUTED - Mar 2022 \nSources: ClinGen",
"entity_name": "GJA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:15:19.926075+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.292",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CEMIP was added\ngene: CEMIP was added to Deafness_IsolatedAndComplex. Sources: ClinGen\ndisputed tags were added to gene: CEMIP.\nMode of inheritance for gene: CEMIP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEMIP were set to Nonsyndromic genetic hearing loss, MONDO:0019497\nReview for gene: CEMIP was set to RED\nAdded comment: ClinGen DISPUTED - Jul 2018 \nSources: ClinGen",
"entity_name": "CEMIP",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:10:26.200329+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.291",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: GJB3.",
"entity_name": "GJB3",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:07:44.672589+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.281",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SIX5.",
"entity_name": "SIX5",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:05:46.682405+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.291",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: TMTC2.",
"entity_name": "TMTC2",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:02:54.173618+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3587",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PDLIM3.",
"entity_name": "PDLIM3",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:02:52.287417+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3587",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: PDLIM3 were changed from Hypertrophic cardiomyopathy to Hypertrophic cardiomyopathy; Dilated cardiomyopathy, MONDO:0005021",
"entity_name": "PDLIM3",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:02:02.638226+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MYL3 as ready",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:02:02.628293+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: myl3 has been classified as Red List (Low Evidence).",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:00:14.964736+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3586",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene PDLIM3 from panel Dilated Cardiomyopathy",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T12:00:13.015572+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: PSEN1 as ready",
"entity_name": "PSEN1",
"entity_type": "gene"
},
{
"created": "2025-11-20T12:00:13.005706+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: psen1 has been classified as Red List (Low Evidence).",
"entity_name": "PSEN1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:59:57.337361+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3585",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene PKP2 from panel Dilated Cardiomyopathy",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T11:59:56.751364+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3585",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PKP2 was added\ngene: PKP2 was added to Mendeliome. Sources: Expert Review Green,Literature\nMode of inheritance for gene: PKP2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PKP2 were set to 15489853; 16567567; 30562116; 35059364; 38050058\nPhenotypes for gene: PKP2 were set to Arrhythmogenic right ventricular dysplasia 9 (MIM#609040); Dilated cardiomyopathy, MONDO:0005021, PKP2-related; hypoplastic left heart syndrome; hydrops fetalis; ventricular septal defect; left ventricular non-compaction",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:59:22.132584+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: PKP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dilated cardiomyopathy, MONDO:0005021; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:57:48.974808+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PSEN1 was added\ngene: PSEN1 was added to Dilated Cardiomyopathy. Sources: ClinGen\ndisputed tags were added to gene: PSEN1.\nMode of inheritance for gene: PSEN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PSEN1 were set to Dilated cardiomyopathy, MONDO:0005021\nReview for gene: PSEN1 was set to RED\nAdded comment: ClinGen DISPUTED - May 2025 \nSources: ClinGen",
"entity_name": "PSEN1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:57:29.488138+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.51",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: MYL3 was added\ngene: MYL3 was added to Dilated Cardiomyopathy. Sources: ClinGen\ndisputed tags were added to gene: MYL3.\nMode of inheritance for gene: MYL3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYL3 were set to Dilated cardiomyopathy, MONDO:0005021\nReview for gene: MYL3 was set to RED\nAdded comment: ClinGen DISPUTED - May 2025 \nSources: ClinGen",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:57:02.968499+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.50",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: PDLIM3 as ready",
"entity_name": "PDLIM3",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:57:02.960575+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.50",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: pdlim3 has been classified as Red List (Low Evidence).",
"entity_name": "PDLIM3",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:56:36.896651+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.50",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PDLIM3 was added\ngene: PDLIM3 was added to Dilated Cardiomyopathy. Sources: ClinGen\ndisputed tags were added to gene: PDLIM3.\nMode of inheritance for gene: PDLIM3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PDLIM3 were set to Dilated cardiomyopathy, MONDO:0005021\nReview for gene: PDLIM3 was set to RED\nAdded comment: ClinGen DISPUTED - May 2025 \nSources: ClinGen",
"entity_name": "PDLIM3",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:39:52.426604+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3584",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:39:32.587703+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.277",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:39:22.453567+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.569",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:39:06.664108+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.594",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:38:58.739779+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 disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:38:49.273138+11:00",
"panel_name": "Ataxia - paediatric",
"panel_id": 271,
"panel_version": "1.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:38:38.311594+11:00",
"panel_name": "Progressive Myoclonic Epilepsy",
"panel_id": 331,
"panel_version": "0.22",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRICKLE1.",
"entity_name": "PRICKLE1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:37:41.856948+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3584",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Source Victorian Clinical Genetics Services was removed from CPA6.\nSource ClinGen was added to CPA6.\nMode of inheritance for gene CPA6 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:37:14.032529+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.277",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Source Victorian Clinical Genetics Services was removed from CPA6.\nSource Australian Genomics Health Alliance Epilepsy Flagship was removed from CPA6.\nSource ClinGen was added to CPA6.\nMode of inheritance for gene CPA6 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:35:25.796244+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.276",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CASR as ready",
"entity_name": "CASR",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:35:25.782708+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.276",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: casr has been classified as Red List (Low Evidence).",
"entity_name": "CASR",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:35:20.071433+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.276",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CASR was added\ngene: CASR was added to Genetic Epilepsy. Sources: ClinGen\ndisputed tags were added to gene: CASR.\nMode of inheritance for gene: CASR was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CASR were set to Epilepsy, MONDO:0005027\nReview for gene: CASR was set to RED\nAdded comment: ClinGen DISPUTED - Mar 2021 \nSources: ClinGen",
"entity_name": "CASR",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:32:14.375693+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3583",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: FAAP24.",
"entity_name": "FAAP24",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:32:06.098158+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3583",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: FAAP24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "FAAP24",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:31:37.396153+11:00",
"panel_name": "Disorders of immune dysregulation",
"panel_id": 229,
"panel_version": "1.34",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: FAAP24.",
"entity_name": "FAAP24",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:31:00.254549+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3583",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: LIMS2.",
"entity_name": "LIMS2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:30:40.844109+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3583",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene LIMS2 from panel Myopathy - paediatric onset",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T11:20:39.024407+11:00",
"panel_name": "Pulmonary Arterial Hypertension",
"panel_id": 3095,
"panel_version": "1.46",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: BMPR1A as ready",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:20:39.013994+11:00",
"panel_name": "Pulmonary Arterial Hypertension",
"panel_id": 3095,
"panel_version": "1.46",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: bmpr1a has been classified as Red List (Low Evidence).",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:20:34.684685+11:00",
"panel_name": "Pulmonary Arterial Hypertension",
"panel_id": 3095,
"panel_version": "1.46",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: BMPR1A was added\ngene: BMPR1A was added to Pulmonary Arterial Hypertension. Sources: ClinGen\ndisputed tags were added to gene: BMPR1A.\nMode of inheritance for gene: BMPR1A was set to Unknown\nPhenotypes for gene: BMPR1A were set to Pulmonary arterial hypertension MONDO:0015924\nReview for gene: BMPR1A was set to RED\nAdded comment: ClinGen DISPUTED - Oct 2022 \nSources: ClinGen",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:18:08.940224+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.111",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: RASA1 as ready",
"entity_name": "RASA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:18:08.929998+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.111",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: rasa1 has been classified as Red List (Low Evidence).",
"entity_name": "RASA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:17:53.065435+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.111",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: RASA1 was added\ngene: RASA1 was added to Rasopathy. Sources: ClinGen\ndisputed tags were added to gene: RASA1.\nMode of inheritance for gene: RASA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RASA1 were set to Noonan syndrome, MONDO:0018997\nReview for gene: RASA1 was set to RED\nAdded comment: ClinGen DISPUTED - Jun 2018 \nSources: ClinGen",
"entity_name": "RASA1",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:16:14.151384+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.110",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: NSUN2 as ready",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:16:14.141171+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.110",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: nsun2 has been classified as Red List (Low Evidence).",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:16:07.695246+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.110",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NSUN2 was added\ngene: NSUN2 was added to Rasopathy. Sources: ClinGen\ndisputed tags were added to gene: NSUN2.\nMode of inheritance for gene: NSUN2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: NSUN2 were set to RASopathy, MONDO:0021060\nReview for gene: NSUN2 was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2019 \nSources: ClinGen",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:14:18.764776+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.109",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: KAT6B as ready",
"entity_name": "KAT6B",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:14:18.754719+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.109",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kat6b has been classified as Red List (Low Evidence).",
"entity_name": "KAT6B",
"entity_type": "gene"
},
{
"created": "2025-11-20T11:14:14.490678+11:00",
"panel_name": "Rasopathy",
"panel_id": 164,
"panel_version": "0.109",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KAT6B was added\ngene: KAT6B was added to Rasopathy. Sources: ClinGen\ndisputed tags were added to gene: KAT6B.\nMode of inheritance for gene: KAT6B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: KAT6B were set to RASopathy, MONDO:0021060\nReview for gene: KAT6B was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2019 \nSources: ClinGen",
"entity_name": "KAT6B",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:58:19.128134+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: PMS1 as ready",
"entity_name": "PMS1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:58:19.116970+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: pms1 has been classified as Red List (Low Evidence).",
"entity_name": "PMS1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:58:15.470421+11:00",
"panel_name": "Colorectal Cancer and Polyposis",
"panel_id": 4371,
"panel_version": "1.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PMS1 was added\ngene: PMS1 was added to Colorectal Cancer and Polyposis. Sources: ClinGen\nrefuted tags were added to gene: PMS1.\nMode of inheritance for gene: PMS1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PMS1 were set to Lynch syndrome, MONDO:0005835\nReview for gene: PMS1 was set to RED\nAdded comment: ClinGen REFUTED - Dec 2023 \nSources: ClinGen",
"entity_name": "PMS1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:57:35.086362+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: RAD50 as ready",
"entity_name": "RAD50",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:57:35.078885+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: rad50 has been classified as Red List (Low Evidence).",
"entity_name": "RAD50",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:57:32.003908+11:00",
"panel_name": "Ovarian Cancer",
"panel_id": 4374,
"panel_version": "1.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: RAD50 was added\ngene: RAD50 was added to Ovarian 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 Familial ovarian cancer, MONDO:0016248\nReview for gene: RAD50 was set to RED\nAdded comment: ClinGen REFUTED - Feb 2024 \nSources: ClinGen",
"entity_name": "RAD50",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:57:14.559167+11:00",
"panel_name": "Early-onset Dementia",
"panel_id": 24,
"panel_version": "1.52",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: SQSTM1 as Amber List (moderate evidence)",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:57:14.552651+11:00",
"panel_name": "Early-onset Dementia",
"panel_id": 24,
"panel_version": "1.52",
"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": "2025-11-20T10:55:44.933112+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: XRCC2 as ready",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:44.917339+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: xrcc2 has been classified as Red List (Low Evidence).",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:40.936095+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: SLX4 as ready",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:40.923334+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: slx4 has been classified as Red List (Low Evidence).",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:36.724192+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: RINT1 as ready",
"entity_name": "RINT1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:36.713755+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: rint1 has been classified as Red List (Low Evidence).",
"entity_name": "RINT1",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:32.646125+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: RAD50 as ready",
"entity_name": "RAD50",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:32.637999+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: rad50 has been classified as Red List (Low Evidence).",
"entity_name": "RAD50",
"entity_type": "gene"
},
{
"created": "2025-11-20T10:55:29.161126+11:00",
"panel_name": "Breast Cancer",
"panel_id": 4375,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: PIK3CA as ready",
"entity_name": "PIK3CA",
"entity_type": "gene"
}
]
}