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{
"count": 220694,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=123",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=121",
"results": [
{
"created": "2025-11-20T16:40:55.128079+11:00",
"panel_name": "Bleeding and Platelet Disorders",
"panel_id": 54,
"panel_version": "1.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: PRKACG.",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:40:50.113649+11:00",
"panel_name": "Bleeding and Platelet Disorders",
"panel_id": 54,
"panel_version": "1.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: PRKACG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:29:45.765995+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.19",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: VCL were changed from Cardiomyopathy, hypertrophic, 15, MIM# 613255 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "VCL",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:29:02.036090+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: VCL.",
"entity_name": "VCL",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:28:52.188156+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: VCL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VCL",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:28:05.244680+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "changed review comment from: ClinGen DISPUTED - Oct 2022; to: AD HCM ClinGen DISPUTED - Oct 2022",
"entity_name": "TRIM63",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:27:54.183646+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: TRIM63: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRIM63",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:26:04.189844+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:25:45.211318+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:25:36.370836+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: MYPN: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:25:33.261843+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:25:14.012553+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:24:59.984617+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:24:42.117026+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYPN were changed from Cardiomyopathy, hypertrophic, 22 (MIM#\t615248) to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:24:07.187904+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYPN.",
"entity_name": "MYPN",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:22:58.086368+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3609",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYOZ2 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:22:57.318487+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3609",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYOZ2 were changed from Cardiomyopathy, hypertrophic, 16 MIM#613838 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:22:43.089624+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3608",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYOZ2.",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:22:29.872037+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3608",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene MYOZ2 from panel Hypertrophic cardiomyopathy_HCM",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T16:20:55.471657+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: MYOZ2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:20:21.845826+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYOZ2 were changed from Cardiomyopathy, hypertrophic, 16 MIM#613838 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:20:15.989533+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYOZ2.",
"entity_name": "MYOZ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:19:18.420724+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3607",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYOM1.",
"entity_name": "MYOM1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:19:03.376843+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3607",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene MYOM1 from panel Hypertrophic cardiomyopathy_HCM",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T16:18:02.829323+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYOM1.",
"entity_name": "MYOM1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:17:56.695031+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: MYOM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYOM1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:14:38.274721+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: KCNQ1 as ready",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:14:38.267802+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcnq1 has been classified as Red List (Low Evidence).",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:14:33.365102+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KCNQ1 was added\ngene: KCNQ1 was added to Hypertrophic cardiomyopathy_HCM. Sources: ClinGen\ndisputed tags were added to gene: KCNQ1.\nMode of inheritance for gene: KCNQ1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: KCNQ1 were set to Hypertrophic cardiomyopathy, MONDO:0005045\nReview for gene: KCNQ1 was set to RED\nAdded comment: ClinGen DISPUTED - May 2022 \nSources: ClinGen",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:13:02.223660+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3606",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYLK2.",
"entity_name": "MYLK2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:12:59.579220+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3606",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene MYLK2 from panel Hypertrophic cardiomyopathy_HCM",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T16:11:57.336078+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYLK2.",
"entity_name": "MYLK2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:11:49.008395+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: MYLK2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYLK2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:10:32.922516+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYH6 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:10:18.137308+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYH6 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:09:56.923152+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYH6 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:09:41.744684+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYH6 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:09:29.490528+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MYH6 were changed from Hypertrophic cardiomyopathy to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:09:03.956892+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MYH6.",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:08:58.796247+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: MYH6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH6",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:08:05.895624+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: DSP as ready",
"entity_name": "DSP",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:08:05.885706+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: dsp has been classified as Red List (Low Evidence).",
"entity_name": "DSP",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:07:56.533431+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: DSP was added\ngene: DSP was added to Hypertrophic cardiomyopathy_HCM. Sources: ClinGen\ndisputed tags were added to gene: DSP.\nMode of inheritance for gene: DSP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DSP were set to Hypertrophic cardiomyopathy, MONDO:0005045\nReview for gene: DSP was set to RED\nAdded comment: ClinGen DISPUTED - Jun 2022 \nSources: ClinGen",
"entity_name": "DSP",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:05:42.631598+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.13",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CASQ2 as ready",
"entity_name": "CASQ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:05:42.621526+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.13",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: casq2 has been classified as Red List (Low Evidence).",
"entity_name": "CASQ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:05:33.023535+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.13",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CASQ2 was added\ngene: CASQ2 was added to Hypertrophic cardiomyopathy_HCM. Sources: ClinGen\ndisputed tags were added to gene: CASQ2.\nMode of inheritance for gene: CASQ2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CASQ2 were set to Hypertrophic cardiomyopathy, MONDO:0005045\nReview for gene: CASQ2 was set to RED\nAdded comment: ClinGen DISPUTED - May 2022 \nSources: ClinGen",
"entity_name": "CASQ2",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:02:42.781098+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3605",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from Hypertrophic cardiomyopathy to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:02:38.774238+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.12",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:02:27.704343+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3604",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag refuted was removed from gene: CALR3.\nTag disputed tag was added to gene: CALR3.",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:02:26.752981+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3604",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene CALR3 from panel Hypertrophic cardiomyopathy_HCM",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T16:02:19.212960+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.13",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:02:04.673150+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.12",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from Hypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:01:49.771345+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.12",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from d)\tHypertrophic cardiomyopathy, MONDO:0005045 to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:01:30.183803+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.12",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CALR3 were changed from Hypertrophic cardiomyopathy to d)\tHypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:01:27.724644+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.11",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag refuted was removed from gene: CALR3.\nTag disputed tag was added to gene: CALR3.",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T16:01:06.927922+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.11",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: CALR3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CALR3",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:59:47.725338+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3603",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: ANKRD1.",
"entity_name": "ANKRD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:59:17.982550+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3603",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: ANKRD1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: None",
"entity_name": "ANKRD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:58:41.368465+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.11",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: ANKRD1 were changed from hypertrophic cardiomyopathy to Hypertrophic cardiomyopathy, MONDO:0005045",
"entity_name": "ANKRD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:58:00.250004+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.10",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: ANKRD1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypertrophic cardiomyopathy, MONDO:0005045; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ANKRD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:57:20.692338+11:00",
"panel_name": "Hypertrophic cardiomyopathy_HCM",
"panel_id": 111,
"panel_version": "1.10",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: ANKRD1.",
"entity_name": "ANKRD1",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:37.019149+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:36.997884+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:22.598605+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:22.589493+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:05.659243+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:56:05.634580+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:50.457686+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:50.440089+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:31.014371+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:30.996800+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.368",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:16.870376+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:16.853316+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:01.595322+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:55:01.571359+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:54:36.275795+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:54:36.264824+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:54:13.751383+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3603",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene KCNE2 from panel Long QT Syndrome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T15:54:12.556352+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3603",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KCNE2 was added\ngene: KCNE2 was added to Mendeliome. Sources: Expert Review Red,Victorian Clinical Genetics Services\ndisputed tags were added to gene: KCNE2.\nMode of inheritance for gene: KCNE2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KCNE2 were set to 31983240; 28794082\nPhenotypes for gene: KCNE2 were set to Long QT syndrome",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:53:59.545444+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.367",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene KCNE2 from panel Long QT Syndrome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T15:53:33.117405+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.366",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCNE2.",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:53:02.594088+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:53:02.571139+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:52:45.677607+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:52:45.669390+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:52:25.755739+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:52:25.747448+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.62",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:51:59.284605+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.61",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KCNE2.",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:51:53.047884+11:00",
"panel_name": "Long QT Syndrome",
"panel_id": 131,
"panel_version": "0.61",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: KCNE2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Long QT syndrome MONDO:0002442; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:50:09.252955+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.366",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: ANK2.",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:49:41.165319+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3602",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene AKAP9 from panel Long QT Syndrome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T15:49:39.996779+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3602",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: AKAP9 was added\ngene: AKAP9 was added to Mendeliome. Sources: Expert Review Red,Victorian Clinical Genetics Services\ndisputed tags were added to gene: AKAP9.\nMode of inheritance for gene: AKAP9 was set to Unknown\nPublications for gene: AKAP9 were set to 31983240\nPhenotypes for gene: AKAP9 were set to long QT syndrome",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:47:46.833123+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3601",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:47:44.680121+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3601",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:47:00.983228+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3601",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene TUBA8 from panel Polymicrogyria and Schizencephaly",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-20T15:46:14.090034+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.470",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: TUBA8.",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:46:05.974092+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: TUBA8.",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:45:58.563954+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.470",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:45:53.300796+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: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2025-11-20T15:45:35.593418+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: TUBA8.",
"entity_name": "TUBA8",
"entity_type": "gene"
}
]
}