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{
"count": 220549,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=112",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=110",
"results": [
{
"created": "2025-11-27T10:41:52.688453+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3675",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene FOXL1 from panel Congenital Heart Defect",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:41:33.844584+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.488",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: FOXL1 as ready",
"entity_name": "FOXL1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:41:33.833679+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.488",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: foxl1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXL1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:41:24.066504+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.488",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FOXL1 was added\ngene: FOXL1 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: FOXL1.\nMode of inheritance for gene: FOXL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FOXL1 were set to Congenital heart disease, MONDO:0005453\nReview for gene: FOXL1 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2023 \nSources: ClinGen",
"entity_name": "FOXL1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:40:36.210047+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3674",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FMO5 from panel Congenital Heart Defect",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:40:34.946832+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3674",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FMO5 was added\ngene: FMO5 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: FMO5.\nMode of inheritance for gene: FMO5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FMO5 were set to Congenital heart disease, MONDO:0005453",
"entity_name": "FMO5",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:40:14.676624+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.487",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: FMO5 as ready",
"entity_name": "FMO5",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:40:14.668897+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.487",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: fmo5 has been classified as Red List (Low Evidence).",
"entity_name": "FMO5",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:40:00.211886+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.487",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FMO5 was added\ngene: FMO5 was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: FMO5.\nMode of inheritance for gene: FMO5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FMO5 were set to Congenital heart disease, MONDO:0005453\nReview for gene: FMO5 was set to RED\nAdded comment: ClinGen DISPUTED - Nov 2023 \nSources: ClinGen",
"entity_name": "FMO5",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:39:52.513130+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.486",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: DTNA as ready",
"entity_name": "DTNA",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:39:52.501908+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.486",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: dtna has been classified as Red List (Low Evidence).",
"entity_name": "DTNA",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:39:06.662305+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3673",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene DTNA from panel Congenital Heart Defect",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:36:26.937933+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3672",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene DTNA from panel Congenital Heart Defect",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:35:42.115833+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.486",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: DTNA was added\ngene: DTNA was added to Congenital Heart Defect. Sources: ClinGen\ndisputed tags were added to gene: DTNA.\nMode of inheritance for gene: DTNA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DTNA were set to Congenital heart disease, MONDO:0005453\nReview for gene: DTNA was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2024 \nSources: ClinGen",
"entity_name": "DTNA",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:32:16.015685+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.485",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: FOXP1 as Red List (low evidence)",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:32:15.999784+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.485",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: foxp1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:31:58.444759+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.485",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: FOXP1 as Red List (low evidence)",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:31:58.428529+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.485",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: foxp1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:31:37.385515+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.484",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: FOXP1.",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:31:30.658354+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.484",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: FOXP1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: congenital heart disease, MONDO:0005453; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXP1",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:19:26.943809+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.286",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: ZDHHC15.",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:18:17.429048+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.573",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMC3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:18:04.224044+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.573",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:17:51.184800+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.572",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:17:30.998506+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.572",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:17:13.123990+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.571",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from Cortical malformations, occipital, MIM#614115 to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:16:59.849692+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.571",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:16:30.207528+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:16:25.935383+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "edited their review of gene: LAMC3: Added comment: Occipital cortical malformations not corpus callosum; Changed phenotypes: Cortical malformations, occipital, MIM#614115; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:15:59.868471+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: LAMC3 as Red List (low evidence)",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:15:59.837163+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:15:57.099468+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: LAMC3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:15:46.194567+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: LAMC3 as Red List (low evidence)",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:15:46.184437+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.570",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:14:20.808275+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.230",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MET were changed from ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:13:47.841546+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MET.",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:13:42.162003+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "edited their review of gene: MET: Added comment: ClinGen DISPUTED - Jan 2021; Changed phenotypes: complex neurodevelopmental disorder, MONDO:0100038; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:13:11.686274+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.455",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: LAMC3 as Green List (high evidence)",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:13:11.674040+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.455",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Green List (High Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:12:58.110746+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.455",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: LAMC3 as Green List (high evidence)",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:12:58.100993+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.455",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Green List (High Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:11:38.346447+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.454",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: MET were changed from ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:11:24.419084+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.454",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: MET was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:10:58.630724+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.453",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: MET.",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:10:51.707779+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.453",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "edited their review of gene: MET: Added comment: ClinGen DISPUTED - Jan 2021; Changed phenotypes: complex neurodevelopmental disorder, MONDO:0100038; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:08:14.698252+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: RELN.",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:08:14.068805+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.453",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene FAAH2 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:06:36.533786+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3671",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CLIC2.",
"entity_name": "CLIC2",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:05:23.855104+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3671",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene EN2 from panel Intellectual disability syndromic and non-syndromic",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T10:05:22.708837+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3671",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: EN2 was added\ngene: EN2 was added to Mendeliome. Sources: Expert Review Red,ClinGen\ndisputed tags were added to gene: EN2.\nMode of inheritance for gene: EN2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: EN2 were set to Complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "EN2",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:05:01.531575+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.452",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: EN2 as ready",
"entity_name": "EN2",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:05:01.523618+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.452",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: en2 has been classified as Red List (Low Evidence).",
"entity_name": "EN2",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:04:53.901258+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.452",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: EN2 was added\ngene: EN2 was added to Intellectual disability syndromic and non-syndromic. Sources: ClinGen\ndisputed tags were added to gene: EN2.\nMode of inheritance for gene: EN2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: EN2 were set to Complex neurodevelopmental disorder, MONDO:0100038\nReview for gene: EN2 was set to RED\nAdded comment: ClinGen DISPUTED - Feb 2021\r\n\r\nhttps://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_91eb2fc6-864c-4a4a-9b2d-0b2bdd695999-2021-02-16T170000.000Z?page=1&size=25&search= \nSources: ClinGen",
"entity_name": "EN2",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:01:35.987875+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3670",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: CNTN4 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:01:35.058251+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3670",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: CNTN4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:00:38.712680+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:00:24.869222+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.230",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:00:12.148507+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.230",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T10:00:08.242656+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: KATNAL2.",
"entity_name": "KATNAL2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:56.638889+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.230",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:38.317622+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.230",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:33.337605+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: KIRREL3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "KIRREL3",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:23.558724+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:10.079561+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag refuted was removed from gene: KIRREL3.\nTag disputed tag was added to gene: KIRREL3.",
"entity_name": "KIRREL3",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:59:02.167165+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:58:56.835243+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag refuted was removed from gene: KIRREL3.\nTag disputed tag was added to gene: KIRREL3.",
"entity_name": "KIRREL3",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:58:44.329496+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:58:30.532604+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:58:16.855863+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:58:02.919152+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.229",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from Intellectual disability; SCA to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:52.883466+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.228",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CNTN4.",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:47.118016+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:46.628554+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:46.610895+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:45.993054+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:45.722075+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:44.686067+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:43.579397+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3669",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:35.331877+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3668",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:15.397156+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3667",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CNTN4.",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:57:00.246079+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3667",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene CNTN4 from panel Intellectual disability syndromic and non-syndromic",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T09:56:47.225815+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.228",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene CNTN4 from panel Intellectual disability syndromic and non-syndromic",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-11-27T09:56:42.521252+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:56:25.274486+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:56:15.802179+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3666",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CNTNAP5 as ready",
"entity_name": "CNTNAP5",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:56:15.789655+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3666",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cntnap5 has been classified as Red List (Low Evidence).",
"entity_name": "CNTNAP5",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:56:11.648571+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:56:09.258280+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.228",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:55:55.274921+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.227",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:55:53.115732+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from complex neurodevelopmental disorder, MONDO:0100038 to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:55:40.189975+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.451",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from Intellectual disability; SCA to complex neurodevelopmental disorder, MONDO:0100038",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:55:35.874283+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.226",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:55:05.578931+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.227",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:55.350960+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.450",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: CNTN4.",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:51.274282+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.227",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:47.523751+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.450",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: CNTN4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: complex neurodevelopmental disorder, MONDO:0100038; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:36.285727+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.227",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:22.732212+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.226",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from Cortical dysplasia-focal epilepsy syndrome, MIM# 610042 to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:54:04.964778+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.226",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: CNTNAP2 were changed from to Cortical dysplasia-focal epilepsy syndrome, MIM# 610042",
"entity_name": "CNTNAP2",
"entity_type": "gene"
},
{
"created": "2025-11-27T09:53:51.323822+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.226",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: CNTNAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CNTNAP2",
"entity_type": "gene"
}
]
}