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