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{
"count": 221413,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1816",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1814",
"results": [
{
"created": "2020-04-29T15:55:23.068684+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Agree, structural brain abnormalities are a feature of more severe FKTN-associated disease, though PCH/cerebellar hypoplasia not prominent (more unusual abnormalities like cerebellar polymicrogyria described).",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:55:23.036168+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fktn has been classified as Amber List (Moderate Evidence).",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:53:59.131754+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FKTN were changed from Cardiomyopathy, dilated, 1X\t611615; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4\t253800; Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4\t613152; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4\t611588; Walker-Warburg syndrome to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4\t253800; Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4\t613152; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4\t611588; Walker-Warburg syndrome",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:43:24.151146+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FKTN as Amber List (moderate evidence)",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:43:24.141635+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fktn has been classified as Amber List (Moderate Evidence).",
"entity_name": "FKTN",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:30:39.499537+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GMPPB as ready",
"entity_name": "GMPPB",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:30:39.490317+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gmppb has been classified as Green List (High Evidence).",
"entity_name": "GMPPB",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:30:28.768885+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GMPPB as Green List (high evidence)",
"entity_name": "GMPPB",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:30:28.758196+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gmppb has been classified as Green List (High Evidence).",
"entity_name": "GMPPB",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:29:38.837084+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMT1 as ready",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:29:38.828166+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomt1 has been classified as Green List (High Evidence).",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:29:34.155411+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: POMT1 as Green List (high evidence)",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:29:34.141586+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomt1 has been classified as Green List (High Evidence).",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:28:40.312524+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISPD as ready",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:28:40.303653+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ispd has been classified as Green List (High Evidence).",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:27:38.311043+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ISPD as Green List (high evidence)",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:27:38.302748+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ispd has been classified as Green List (High Evidence).",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:26:30.167198+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIAA1109 as ready",
"entity_name": "KIAA1109",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:26:30.154720+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa1109 has been classified as Green List (High Evidence).",
"entity_name": "KIAA1109",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:26:27.324640+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIAA1109 were changed from to Alkuraya-Kucinskas syndrome, MIM# 617822",
"entity_name": "KIAA1109",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:25:56.934831+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIAA1109 were set to ",
"entity_name": "KIAA1109",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:25:25.470578+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIAA1109 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIAA1109",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:24:25.333949+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMGNT2 as ready",
"entity_name": "POMGNT2",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:24:25.324804+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomgnt2 has been classified as Green List (High Evidence).",
"entity_name": "POMGNT2",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:24:20.378393+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: POMGNT2 as Green List (high evidence)",
"entity_name": "POMGNT2",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:24:20.369243+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomgnt2 has been classified as Green List (High Evidence).",
"entity_name": "POMGNT2",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:23:21.262953+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMGNT1 as ready",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:23:21.249149+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomgnt1 has been classified as Green List (High Evidence).",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:23:14.644285+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: POMGNT1 as Green List (high evidence)",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:23:14.633750+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomgnt1 has been classified as Green List (High Evidence).",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:22:04.615647+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LARGE1 as ready",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:22:04.603208+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: large1 has been classified as Green List (High Evidence).",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:22:00.814895+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LARGE1 were set to PMID: 17878207; 19067344; PMID: 24709677",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:21:37.133771+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LARGE1 as Green List (high evidence)",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:21:37.123008+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: large1 has been classified as Green List (High Evidence).",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:20:57.152327+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: LARGE1.",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:16:15.545422+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MACF1 as ready",
"entity_name": "MACF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:16:15.536306+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: macf1 has been classified as Green List (High Evidence).",
"entity_name": "MACF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:16:08.814814+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MACF1 as Green List (high evidence)",
"entity_name": "MACF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:16:08.803290+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: macf1 has been classified as Green List (High Evidence).",
"entity_name": "MACF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:14:23.300680+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCOF1 as ready",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:14:23.288748+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcof1 has been classified as Green List (High Evidence).",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:14:19.034519+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCOF1 were changed from to Treacher Collins syndrome 1, MIM# 154500",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:13:47.387591+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCOF1 were set to ",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:13:17.995736+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:12:45.250926+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TCOF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12444270, 15150774, 21951868; Phenotypes: Treacher Collins syndrome 1, MIM# 154500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:11:55.819566+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCOF1 as ready",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:11:55.808558+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcof1 has been classified as Green List (High Evidence).",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:11:46.924069+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCOF1 were changed from to Treacher Collins syndrome 1, MIM# 154500",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:11:25.767497+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2657",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCOF1 were set to ",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:11:07.359441+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:10:24.516447+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TCOF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12444270, 15150774, 21951868; Phenotypes: Treacher Collins syndrome 1, MIM# 154500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:02:26.256893+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCOF1 as ready",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:02:26.238973+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcof1 has been classified as Green List (High Evidence).",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:02:23.780648+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCOF1 were changed from to Treacher Collins syndrome 1, MIM# 154500",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:01:48.192058+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCOF1 were set to ",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T15:01:19.147601+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCOF1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:59:55.758823+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: EMX2.",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:59:44.785921+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EMX2 as ready",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:59:44.776721+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:59:27.051658+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EMX2 were changed from to Schizencephaly, MIM# 269160",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:58:53.196121+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2608",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EMX2 were set to ",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:58:17.763630+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EMX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:57:45.693609+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EMX2 as Amber List (moderate evidence)",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:57:45.684456+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:57:01.306808+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2605",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EMX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:56:18.076928+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EMX2 as ready",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:56:18.063825+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Red List (Low Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:56:15.071931+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EMX2 were changed from to Schizencephaly, MIM# 269160",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:55:49.131101+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EMX2 were set to 8528262; 9359037; 9153481; 9153481; 18409201",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:55:24.004776+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EMX2 were set to ",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:55:03.956599+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EMX2 as Red List (low evidence)",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:55:03.944214+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Red List (Low Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:54:39.285606+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EMX2 as Red List (low evidence)",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:54:39.262354+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Red List (Low Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:54:07.249937+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EMX2: Rating: RED; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: None",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:52:46.968464+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EMX2 as ready",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:52:46.959174+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:52:43.507609+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EMX2 were changed from to Schizencephaly, MIM# 269160",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:52:05.496751+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: EMX2.",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:51:59.982157+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EMX2 were set to ",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:51:28.756548+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.687",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EMX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:50:59.805586+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EMX2 as Amber List (moderate evidence)",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:50:59.796526+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: emx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:49:53.576314+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: EMX2.",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:49:46.785314+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EMX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:29:29.824734+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPAA1 as ready",
"entity_name": "GPAA1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:29:29.815933+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpaa1 has been classified as Green List (High Evidence).",
"entity_name": "GPAA1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:29:27.169497+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPAA1 were changed from to Glycosylphosphatidylinositol biosynthesis defect 15, MIM# 617810",
"entity_name": "GPAA1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:29:03.647100+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPAA1 were set to ",
"entity_name": "GPAA1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:28:35.420103+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPAA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPAA1",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:26:15.392110+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PPP1CB as ready",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:26:15.383095+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ppp1cb has been classified as Red List (Low Evidence).",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:26:10.849569+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPP1CB were changed from to Noonan syndrome-like disorder with loose anagen hair 2 (MIM#617506)",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:25:47.278614+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PPP1CB were set to ",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:25:23.540643+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PPP1CB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:24:58.335954+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PPP1CB as Red List (low evidence)",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:24:58.327039+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ppp1cb has been classified as Red List (Low Evidence).",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:24:28.726849+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PPP1CB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Noonan syndrome-like disorder with loose anagen hair 2 (MIM#617506); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PPP1CB",
"entity_type": "gene"
},
{
"created": "2020-04-29T14:21:35.741255+10:00",
"panel_name": "Cerebellar and Pontocerebellar Hypoplasia",
"panel_id": 72,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXP1 as ready",
"entity_name": "FOXP1",
"entity_type": "gene"
}
]
}