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{
"count": 220966,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1025",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1023",
"results": [
{
"created": "2022-01-24T20:23:27.578310+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CSNK2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:22:58.639819+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CSNK2B: Rating: GREEN; Mode of pathogenicity: None; Publications: 28585349, 28762608; Phenotypes: Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:21:49.301901+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CSNK2B as ready",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:21:49.291016+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: csnk2b has been classified as Green List (High Evidence).",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:21:38.978096+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CSNK2B were changed from to Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:21:14.400189+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CSNK2B were set to ",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:20:51.201913+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CSNK2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:20:30.712090+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CSNK2B: Rating: GREEN; Mode of pathogenicity: None; Publications: 28585349, 28762608; Phenotypes: Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CSNK2B",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:54.188869+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNU4ATAC as ready",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:54.179488+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnu4atac has been classified as Green List (High Evidence).",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:53.713349+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNU4ATAC as ready",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:53.701190+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnu4atac has been classified as Green List (High Evidence).",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:39.495652+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNU4ATAC as Green List (high evidence)",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:39.484312+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnu4atac has been classified as Green List (High Evidence).",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:14:23.858615+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RNU4ATAC was added\ngene: RNU4ATAC was added to Syndromic Retinopathy. Sources: Expert Review\nMode of inheritance for gene: RNU4ATAC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RNU4ATAC were set to 2801768; 29265708; 30368667\nPhenotypes for gene: RNU4ATAC were set to Roifman syndrome, MIM#\t616651; Lowry-Wood syndrome, MIM#\t226960\nReview for gene: RNU4ATAC was set to GREEN\nAdded comment: Retinal dystrophy reported. \nSources: Expert Review",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:09:51.893235+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PACS1 as ready",
"entity_name": "PACS1",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:09:51.875750+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pacs1 has been classified as Green List (High Evidence).",
"entity_name": "PACS1",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:09:47.156170+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PACS1 were changed from 615009 to Schuurs-Hoeijmakers syndrome, MIM#\t615009",
"entity_name": "PACS1",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:08:59.599609+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PACS1 as Green List (high evidence)",
"entity_name": "PACS1",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:08:59.587361+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pacs1 has been classified as Green List (High Evidence).",
"entity_name": "PACS1",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:07:19.192054+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCAPD3 as ready",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:07:19.181901+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncapd3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:07:11.195244+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCAPD3 were changed from to Microcephaly 22, primary, autosomal recessive, MIM# 617984",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:06:51.505079+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCAPD3 were set to ",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:06:31.218403+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCAPD3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:06:11.062133+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NCAPD3 as Amber List (moderate evidence)",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:06:11.051064+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncapd3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T20:05:53.158414+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NCAPD3: Rating: AMBER; Mode of pathogenicity: None; Publications: 27737959; Phenotypes: Microcephaly 22, primary, autosomal recessive, MIM# 617984; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NCAPD3",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:06:56.305688+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC5A6 as ready",
"entity_name": "SLC5A6",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:06:56.295060+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc5a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC5A6",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:06:48.968306+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC5A6 as Green List (high evidence)",
"entity_name": "SLC5A6",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:06:48.958734+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc5a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC5A6",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:06:33.824246+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC5A6 was added\ngene: SLC5A6 was added to Hereditary Neuropathy - complex. Sources: Literature\nMode of inheritance for gene: SLC5A6 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC5A6 were set to 35013551\nPhenotypes for gene: SLC5A6 were set to Neurodegeneration, infantile-onset, biotin-responsive, MIM#\t618973\nReview for gene: SLC5A6 was set to GREEN\nAdded comment: Multi-system potentially treatable disorder.\r\n\r\nFive individuals from three families reported with motor neuropathies. \nSources: Literature",
"entity_name": "SLC5A6",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:56.927825+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP2C8 as ready",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:56.917773+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp2c8 has been classified as Red List (Low Evidence).",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:48.848929+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP2C8 were changed from to {Drug metabolism, altered, CYP2C8-related} 618018",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:30.473736+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYP2C8 as Red List (low evidence)",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:30.457780+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp2c8 has been classified as Red List (Low Evidence).",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T19:02:12.444755+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP2C8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Drug metabolism, altered, CYP2C8-related} 618018; Mode of inheritance: None",
"entity_name": "CYP2C8",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:56:29.321288+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED25 as ready",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:56:29.311409+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med25 has been classified as Green List (High Evidence).",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:56:21.576146+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MED25 as Green List (high evidence)",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:56:21.556485+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med25 has been classified as Green List (High Evidence).",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:42.941342+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SHMT2 as ready",
"entity_name": "SHMT2",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:42.931826+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: shmt2 has been classified as Green List (High Evidence).",
"entity_name": "SHMT2",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:34.570515+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SHMT2 as Green List (high evidence)",
"entity_name": "SHMT2",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:34.554763+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: shmt2 has been classified as Green List (High Evidence).",
"entity_name": "SHMT2",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:08.377044+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAST1 as ready",
"entity_name": "MAST1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:55:08.364617+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mast1 has been classified as Green List (High Evidence).",
"entity_name": "MAST1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:59.645407+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MAST1 as Green List (high evidence)",
"entity_name": "MAST1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:59.634657+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mast1 has been classified as Green List (High Evidence).",
"entity_name": "MAST1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:33.406119+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAPK8IP3 as ready",
"entity_name": "MAPK8IP3",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:33.395342+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mapk8ip3 has been classified as Green List (High Evidence).",
"entity_name": "MAPK8IP3",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:24.557728+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MAPK8IP3 as Green List (high evidence)",
"entity_name": "MAPK8IP3",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:54:24.545884+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mapk8ip3 has been classified as Green List (High Evidence).",
"entity_name": "MAPK8IP3",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:53:59.299224+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAP1B as ready",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:53:59.288793+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: map1b has been classified as Green List (High Evidence).",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:53:54.826604+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MAP1B were changed from polymicrogyria; PVNH; Periventricular nodular heterotopia 9, MIM# 618918 to Polymicrogyria; Periventricular nodular heterotopia 9, MIM# 618918",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:53:27.453038+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MAP1B as Green List (high evidence)",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:53:27.443149+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: map1b has been classified as Green List (High Evidence).",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:55.647480+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ASTN1 as ready",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:55.636950+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: astn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:51.568544+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ASTN1 were set to 29706646; 11861479",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:38.203739+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ASTN1 as Amber List (moderate evidence)",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:38.194735+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: astn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:01.699678+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE3A as ready",
"entity_name": "PDE3A",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:52:01.686896+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde3a has been classified as Green List (High Evidence).",
"entity_name": "PDE3A",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:51:56.556213+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE3A as Green List (high evidence)",
"entity_name": "PDE3A",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:51:56.542358+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde3a has been classified as Green List (High Evidence).",
"entity_name": "PDE3A",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:51:13.493922+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HYAL1 as ready",
"entity_name": "HYAL1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:51:13.483333+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hyal1 has been classified as Red List (Low Evidence).",
"entity_name": "HYAL1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:51:04.717566+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HYAL1 were changed from MUCOPOLYSACCHARIDOSIS TYPE 9 to Mucopolysaccharidosis type IX, MIM# 601492; MONDO:0011093",
"entity_name": "HYAL1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:50:51.159873+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HYAL1 were set to ",
"entity_name": "HYAL1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:50:16.370882+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FMN1 as ready",
"entity_name": "FMN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:50:16.361145+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fmn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FMN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:50:01.672355+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FMN1 as Amber List (moderate evidence)",
"entity_name": "FMN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:50:01.659172+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fmn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FMN1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:49:24.352767+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSD17B10 as ready",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:49:24.342186+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsd17b10 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:49:17.663579+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSD17B10 were changed from 2-METHYL-3-HYDROXYBUTYRYL-COA DEHYDROGENASE DEFICIENCY; MENTAL RETARDATION SYNDROMIC X-LINKED TYPE 10 to HSD10 mitochondrial disease, MIM# 300438",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:47:55.382510+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HSD17B10 as Amber List (moderate evidence)",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:47:55.371742+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsd17b10 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:47:11.225840+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HPGD as ready",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:47:11.213295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hpgd has been classified as Red List (Low Evidence).",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:47:01.967587+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HPGD were changed from CRANIOOSTEOARTHROPATHY to Hypertrophic osteoarthropathy, primary, autosomal recessive 1 MIM#259100; Cranioosteoarthropathy MIM#259100",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:46:49.492065+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HPGD were set to ",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:46:17.877110+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAT1 as ready",
"entity_name": "FAT1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:46:17.864913+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fat1 has been classified as Green List (High Evidence).",
"entity_name": "FAT1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:46:09.822493+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAT1 as Green List (high evidence)",
"entity_name": "FAT1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:46:09.812587+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fat1 has been classified as Green List (High Evidence).",
"entity_name": "FAT1",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:45:39.372518+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HPGD as ready",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:45:39.360085+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hpgd has been classified as Green List (High Evidence).",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:45:29.778048+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HPGD were changed from to Hypertrophic osteoarthropathy, primary, autosomal recessive 1 MIM#259100; Cranioosteoarthropathy MIM#259100",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:44:59.453383+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HPGD were set to ",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:44:36.887806+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HPGD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HPGD",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:43:57.405310+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLMN as ready",
"entity_name": "GLMN",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:43:57.394925+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glmn has been classified as Green List (High Evidence).",
"entity_name": "GLMN",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:43:49.326615+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLMN were changed from to Glomuvenous malformations MIM#138000",
"entity_name": "GLMN",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:43:29.218303+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLMN were set to ",
"entity_name": "GLMN",
"entity_type": "gene"
},
{
"created": "2022-01-24T18:43:10.310902+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLMN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GLMN",
"entity_type": "gene"
}
]
}