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{
"count": 221416,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=441",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=439",
"results": [
{
"created": "2024-05-30T13:16:48.027771+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TGM6 as ready",
"entity_name": "TGM6",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:16:48.011482+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgm6 has been classified as Red List (Low Evidence).",
"entity_name": "TGM6",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:16:42.208492+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TGM6 as Red List (low evidence)",
"entity_name": "TGM6",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:16:42.193977+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgm6 has been classified as Red List (Low Evidence).",
"entity_name": "TGM6",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:53.108694+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOR1A as ready",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:53.089027+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1a has been classified as Red List (Low Evidence).",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:48.252680+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOR1A as Red List (low evidence)",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:48.228278+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1a has been classified as Red List (Low Evidence).",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:00.925453+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSC2 as ready",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:15:00.904871+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsc2 has been classified as Red List (Low Evidence).",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:56.430422+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSC2 as Red List (low evidence)",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:56.408805+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsc2 has been classified as Red List (Low Evidence).",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:07.251789+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSHR as ready",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:07.236539+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tshr has been classified as Red List (Low Evidence).",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:02.196540+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSHR as Red List (low evidence)",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2024-05-30T13:14:02.164558+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tshr has been classified as Red List (Low Evidence).",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2024-05-30T12:22:45.816785+10:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: AAAS: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2024-05-30T12:22:38.549740+10:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: AAAS: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2024-05-30T12:22:17.946752+10:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: AAAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Achalasia-addisonianism-alacrimia syndrome, MIM# 231550; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:20:52.632536+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SSR4 as ready",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:20:52.618289+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ssr4 has been classified as Green List (High Evidence).",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:20:48.080869+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SSR4 were changed from to Congenital disorder of glycosylation, type Iy, MIM# 300934",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:20:13.115353+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6018",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SSR4 were set to ",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:19:35.460950+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6017",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SSR4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:18:43.800610+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SSR4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Iy, MIM# 300934; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "SSR4",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:17:09.284356+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RELN as ready",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:17:09.269748+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: reln has been classified as Green List (High Evidence).",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:17:01.601399+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RELN were set to ",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:16:12.453521+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RELN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lissencephaly 2 (Norman-Roberts type), MIM# 257320; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:15:49.595963+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RELN were changed from to Lissencephaly 2 (Norman-Roberts type), MIM# 257320",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-30T07:15:11.257010+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RELN was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-29T22:29:02.765373+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6013",
"user_name": "Anissa Johnson",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2024-05-29T20:37:25.514896+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6013",
"user_name": "Tashunka Taylor-Miller",
"item_type": "entity",
"text": "changed review comment from: 7 individuals from 4 families with biallelic variants, and 13 individuals from 7 families with monoallelic (heterozygous) variants of RELN and frontotemporal or temporal-predominant lissencephaly variant. Associated features: intellectual disability (16/20), seizures (5/20), unprovoked aggression (6/20), sleep disturbance (7/20)\r\nVariant spectrum includes: loss of function, missense, splice-site variants.\r\n\r\nMRI features include: anterior-predominant “thin”lisencephaly pachygyria with cerebellar hypoplasia\r\nBiallelic variants are associated with a severe phenotype that includes cerebellar hypoplasia. \r\nMonoallelic variants are associated with incomplete penetrance and variable expressivity (eg: one adult with abnormal MRI but normal intelligence and neurological profile).; to: 7 individuals from 4 families with biallelic variants, and 13 individuals from 7 families with monoallelic (heterozygous) variants of RELN and frontotemporal or temporal-predominant lissencephaly variant. Associated features: intellectual disability (16/20), seizures (5/20), unprovoked aggression (6/20), sleep disturbance (7/20)\r\nVariant spectrum includes: loss of function, missense, splice-site variants.\r\n\r\nMRI features include: anterior-predominant “thin” lisencephaly pachygyria with cerebellar hypoplasia.\r\nBiallelic variants are associated with a severe phenotype that includes cerebellar hypoplasia. \r\nMonoallelic variants are associated with incomplete penetrance and variable expressivity (eg: one adult with abnormal MRI but normal intelligence and neurological profile).",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-29T20:36:36.202469+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6013",
"user_name": "Tashunka Taylor-Miller",
"item_type": "entity",
"text": "edited their review of gene: RELN: Changed publications: PMID: 35769015, PMID: 29671837",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-29T20:36:10.364283+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6013",
"user_name": "Tashunka Taylor-Miller",
"item_type": "entity",
"text": "reviewed gene: RELN: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 35769015, 29671837; Phenotypes: OMIM *600514, HP:0001339, DOID:0070338; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:03:43.248375+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTCF as ready",
"entity_name": "CTCF",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:03:43.229537+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctcf has been classified as Red List (Low Evidence).",
"entity_name": "CTCF",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:03:37.579812+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CTCF as Red List (low evidence)",
"entity_name": "CTCF",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:03:37.566999+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctcf has been classified as Red List (Low Evidence).",
"entity_name": "CTCF",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:02:40.183528+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCN7 as ready",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:02:40.167483+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn7 has been classified as Red List (Low Evidence).",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:02:31.832428+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLCN7 as Red List (low evidence)",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:02:31.801006+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn7 has been classified as Red List (Low Evidence).",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:01:43.268678+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHD7 as ready",
"entity_name": "CHD7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:01:43.253307+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CHD7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:01:34.322962+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHD7 as Amber List (moderate evidence)",
"entity_name": "CHD7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:01:34.309473+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CHD7",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:00:48.353920+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHD4 as ready",
"entity_name": "CHD4",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:00:48.337424+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd4 has been classified as Red List (Low Evidence).",
"entity_name": "CHD4",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:00:43.882507+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHD4 as Red List (low evidence)",
"entity_name": "CHD4",
"entity_type": "gene"
},
{
"created": "2024-05-29T18:00:43.869109+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd4 has been classified as Red List (Low Evidence).",
"entity_name": "CHD4",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:57.426692+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHCHD10 as ready",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:57.403247+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chchd10 has been classified as Red List (Low Evidence).",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:52.148554+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHCHD10 as Red List (low evidence)",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:52.134578+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chchd10 has been classified as Red List (Low Evidence).",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:06.102977+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CAMK2G as ready",
"entity_name": "CAMK2G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:06.090933+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: camk2g has been classified as Red List (Low Evidence).",
"entity_name": "CAMK2G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:01.601145+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CAMK2G as Red List (low evidence)",
"entity_name": "CAMK2G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:59:01.586302+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: camk2g has been classified as Red List (Low Evidence).",
"entity_name": "CAMK2G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:58:16.552323+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CAMK2B as ready",
"entity_name": "CAMK2B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:58:16.538786+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: camk2b has been classified as Red List (Low Evidence).",
"entity_name": "CAMK2B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:58:11.532395+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CAMK2B as Red List (low evidence)",
"entity_name": "CAMK2B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:58:11.507375+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: camk2b has been classified as Red List (Low Evidence).",
"entity_name": "CAMK2B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:57:28.678095+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNA1G as ready",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:57:28.665492+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1g has been classified as Green List (High Evidence).",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:57:14.650254+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CACNA1G as Green List (high evidence)",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:57:14.613295+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1g has been classified as Green List (High Evidence).",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:56:31.479151+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNA1D as ready",
"entity_name": "CACNA1D",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:56:31.464465+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1d has been classified as Amber List (Moderate Evidence).",
"entity_name": "CACNA1D",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:56:26.077735+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CACNA1D as Amber List (moderate evidence)",
"entity_name": "CACNA1D",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:56:26.063628+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1d has been classified as Amber List (Moderate Evidence).",
"entity_name": "CACNA1D",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:55:35.707384+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP6V1A as ready",
"entity_name": "ATP6V1A",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:55:35.694968+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp6v1a has been classified as Red List (Low Evidence).",
"entity_name": "ATP6V1A",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:55:31.188695+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP6V1A as Red List (low evidence)",
"entity_name": "ATP6V1A",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:55:31.171194+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp6v1a has been classified as Red List (Low Evidence).",
"entity_name": "ATP6V1A",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:54:40.603872+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP1A2 as ready",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:54:40.592110+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp1a2 has been classified as Red List (Low Evidence).",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:54:36.035025+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP1A2 as Red List (low evidence)",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:54:36.019260+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp1a2 has been classified as Red List (Low Evidence).",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:53:55.465278+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARID1B as ready",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:53:55.452453+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arid1b has been classified as Red List (Low Evidence).",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:53:48.380261+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ARID1B as Red List (low evidence)",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2024-05-29T17:53:48.369081+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arid1b has been classified as Red List (Low Evidence).",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:58:25.607642+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNM2 as ready",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:58:25.593548+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnm2 has been classified as Red List (Low Evidence).",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:58:17.938399+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNM2 as Red List (low evidence)",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:58:17.922475+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnm2 has been classified as Red List (Low Evidence).",
"entity_name": "DNM2",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:44:16.911848+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.213",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB4A were set to 34531397; 33528536",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:43:29.901310+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBG1 as ready",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:43:29.888185+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubg1 has been classified as Red List (Low Evidence).",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:43:24.668407+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TUBG1 as Red List (low evidence)",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:43:24.652607+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubg1 has been classified as Red List (Low Evidence).",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:42:40.763058+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE3A were set to PMID: 33528536",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:41:53.327916+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB18 as ready",
"entity_name": "ZBTB18",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:41:53.310767+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb18 has been classified as Red List (Low Evidence).",
"entity_name": "ZBTB18",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:41:47.257217+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZBTB18 as Red List (low evidence)",
"entity_name": "ZBTB18",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:41:47.233413+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb18 has been classified as Red List (Low Evidence).",
"entity_name": "ZBTB18",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:40:58.124655+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZEB2 were set to 33528536; 33098801",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:40:07.291849+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ITPR1 were set to 28826917; 25981959; 22986007",
"entity_name": "ITPR1",
"entity_type": "gene"
},
{
"created": "2024-05-29T16:39:14.042124+10:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPTBN2 were set to 31066025; 25981959; 31721007",
"entity_name": "SPTBN2",
"entity_type": "gene"
}
]
}