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{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1801",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1799",
"results": [
{
"created": "2020-05-12T15:09:28.380311+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.35",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: PCCB was added\ngene: PCCB was added to Stroke. Sources: Literature\nMode of inheritance for gene: PCCB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PCCB were set to 30356112; 7769171; 6497733; 30037889; 18986243\nReview for gene: PCCB was set to GREEN\nAdded comment: Metabolic stroke can be a feature of the condition. \nSources: Literature",
"entity_name": "PCCB",
"entity_type": "gene"
},
{
"created": "2020-05-12T15:02:06.844466+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.34",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: PCCA as Green List (high evidence)",
"entity_name": "PCCA",
"entity_type": "gene"
},
{
"created": "2020-05-12T15:02:06.833281+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.34",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: pcca has been classified as Green List (High Evidence).",
"entity_name": "PCCA",
"entity_type": "gene"
},
{
"created": "2020-05-12T12:54:42.049444+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.33",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: PCCA was added\ngene: PCCA was added to Stroke. Sources: Literature\nMode of inheritance for gene: PCCA was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PCCA were set to 21986446; 18986243; 20142522\nReview for gene: PCCA was set to GREEN\nAdded comment: Metabolic stroke can be a feature of the condition. \nSources: Literature",
"entity_name": "PCCA",
"entity_type": "gene"
},
{
"created": "2020-05-12T12:09:44.388521+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.32",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: NF1 as Green List (high evidence)",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2020-05-12T12:09:44.379476+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.32",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: nf1 has been classified as Green List (High Evidence).",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2020-05-12T12:09:05.591804+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.31",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: NF1 was added\ngene: NF1 was added to Stroke. Sources: Literature\nMode of inheritance for gene: NF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NF1 were set to 31080139; 30356112; 8157015; 31279841\nPhenotypes for gene: NF1 were set to Neurofibromatosis, type 1 MIM#162200\nReview for gene: NF1 was set to GREEN\nAdded comment: Stroke can be a feature of the condition, with diolicoectasia, occlusion, and MoyaMoya-like subtypes reported. \nSources: Literature",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:30:38.881002+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALX3 as Red List (low evidence)",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:30:38.867196+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alx3 has been classified as Red List (Low Evidence).",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:30:09.721853+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ALX3: Added comment: Polydactyly not specifically associated with FND1. One family reported in 8362915, but polydactyly considered to be a separate feature.; Changed rating: RED; Changed publications: 19409524, 8362915",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:29:07.848614+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALX3 as ready",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:29:07.839529+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alx3 has been classified as Green List (High Evidence).",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:29:05.223926+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALX3 were changed from to Frontonasal dysplasia 1, MIM#136760",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:27:25.860309+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALX3 were set to ",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:23:58.264496+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:23:18.167257+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B9D2 as ready",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:23:18.156179+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b9d2 has been classified as Green List (High Evidence).",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:23:15.215645+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D2 were changed from to Joubert syndrome 34, MIM#614175; Meckel syndrome 10, MIM#614175",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:22:45.917739+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B9D2 were set to ",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2020-05-12T11:22:22.775368+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B9D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2020-05-12T09:17:39.226158+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.30",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: HBB as Green List (high evidence)",
"entity_name": "HBB",
"entity_type": "gene"
},
{
"created": "2020-05-12T09:17:39.214994+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.30",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: hbb has been classified as Green List (High Evidence).",
"entity_name": "HBB",
"entity_type": "gene"
},
{
"created": "2020-05-12T09:17:17.196844+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.29",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: HBB was added\ngene: HBB was added to Stroke. Sources: Literature\nMode of inheritance for gene: HBB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HBB were set to 30356112; 19589461; 7782612; 20301551\nPhenotypes for gene: HBB were set to Sickle cell anemia MIM#603903\nReview for gene: HBB was set to GREEN\nAdded comment: Stroke can be a feature of sickle cell anemia, with the following subtypes reported: large artery non-atherosclerosis aneurysms, venous thrombosis, and arterial thrombosis. \nSources: Literature",
"entity_name": "HBB",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:56:54.621661+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.28",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: GUCY1A3 as ready",
"entity_name": "GUCY1A3",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:56:54.612645+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.28",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gucy1a3 has been classified as Green List (High Evidence).",
"entity_name": "GUCY1A3",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:56:47.047112+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.28",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: GUCY1A3 as Green List (high evidence)",
"entity_name": "GUCY1A3",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:56:47.033959+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.28",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gucy1a3 has been classified as Green List (High Evidence).",
"entity_name": "GUCY1A3",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:56:36.326408+10:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "0.27",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GUCY1A3 was added\ngene: GUCY1A3 was added to Stroke. Sources: Literature\nMode of inheritance for gene: GUCY1A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GUCY1A3 were set to 24581742; 26777256\nPhenotypes for gene: GUCY1A3 were set to Moyamoya 6 with achalasia MIM#615750\nReview for gene: GUCY1A3 was set to GREEN\nAdded comment: Ischaemic stroke has been reported in at least one individual from five families. \nSources: Literature",
"entity_name": "GUCY1A3",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:39:17.156592+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.21",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: GFI1B as ready",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:39:17.147954+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.21",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gfi1b has been classified as Green List (High Evidence).",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:39:10.362833+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2807",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: GFI1B as ready",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:39:10.354024+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2807",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gfi1b has been classified as Green List (High Evidence).",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:37:17.320783+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2807",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: GFI1B as Green List (high evidence)",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:37:17.312056+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2807",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gfi1b has been classified as Green List (High Evidence).",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:36:49.232892+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2806",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GFI1B was added\ngene: GFI1B was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: GFI1B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GFI1B were set to 24325358; 23927492; 28041820; 11825872\nPhenotypes for gene: GFI1B were set to Bleeding disorder, platelet-type, 17 MIM#187900\nReview for gene: GFI1B was set to GREEN\nAdded comment: Three families with a heterozygous variant and one case with a homozygous variant, with supporting in vitro functional assays. A null mouse model contained erythroid and megakaryocytic precursors arrested in their development. \nSources: Literature",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:35:44.950762+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.21",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: GFI1B as Green List (high evidence)",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:35:44.940205+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.21",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gfi1b has been classified as Green List (High Evidence).",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T08:35:00.701934+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.20",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GFI1B was added\ngene: GFI1B was added to Bleeding Disorders. Sources: Literature\nMode of inheritance for gene: GFI1B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GFI1B were set to 24325358; 23927492; 28041820; 11825872\nPhenotypes for gene: GFI1B were set to Bleeding disorder, platelet-type, 17 MIM#187900\nReview for gene: GFI1B was set to GREEN\nAdded comment: Three families with a heterozygous variant and one case with a homozygous variant, with supporting in vitro functional assays. A null mouse model contained erythroid and megakaryocytic precursors arrested in their development. \nSources: Literature",
"entity_name": "GFI1B",
"entity_type": "gene"
},
{
"created": "2020-05-12T07:31:24.452163+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2805",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "reviewed gene: MOGS: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 31925597; Phenotypes: Congenital disorder of glycosylation, type IIb 606056; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MOGS",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:13:36.660086+10:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATL1 were changed from Spastic paraplegia 3A, autosomal dominant MIM#182600 to Hereditary sensory neuropathy type ID, MIM 613708; Spastic paraplegia 3A, MIM 182600; Hereditary spastic paraplegia, AR",
"entity_name": "ATL1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:13:15.153977+10:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATL1 were set to ",
"entity_name": "ATL1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:13:05.666371+10:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATL1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ATL1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:12:53.052911+10:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ATL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 16401858, 16537571, 17657515, 28396731, 24473461, 26888483; Phenotypes: Hereditary sensory neuropathy type ID, MIM 613708, Spastic paraplegia 3A, MIM 182600, Hereditary spastic paraplegia, AR; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ATL1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:08:12.457989+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2635",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKD1 as ready",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:08:12.445984+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2635",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkd1 has been classified as Green List (High Evidence).",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:08:08.201973+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2635",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKD1 were changed from to Congenital heart defects and ectodermal dysplasia, 617364",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:07:34.894162+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRKD1 were set to ",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:07:00.297779+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRKD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:06:26.396721+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRKD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27479907; Phenotypes: Congenital heart defects and ectodermal dysplasia, 617364; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:05:10.234486+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKD1 as ready",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:05:10.223789+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkd1 has been classified as Green List (High Evidence).",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:05:07.910766+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKD1 were changed from to Congenital heart defects and ectodermal dysplasia, 617364",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:04:40.266661+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRKD1 were set to ",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:04:11.932906+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRKD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:03:40.326757+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRKD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27479907; Phenotypes: Congenital heart defects and ectodermal dysplasia, 617364; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:02:26.950489+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKD1 as ready",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:02:26.941533+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkd1 has been classified as Green List (High Evidence).",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:02:19.060559+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKD1 were changed from to Congenital heart defects and ectodermal dysplasia, 617364",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:01:57.302194+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRKD1 were set to ",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:01:37.745973+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRKD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKD1",
"entity_type": "gene"
},
{
"created": "2020-05-11T21:00:18.605284+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: JPH2.",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:59:37.365921+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NODAL.",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:59:20.721216+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NODAL.",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:59:03.727099+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NODAL.",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:58:46.158176+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JPH2 as ready",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:58:46.152352+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Likely founder effect.",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:58:46.111206+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jph2 has been classified as Red List (Low Evidence).",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:58:25.890546+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: JPH2 as Red List (low evidence)",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:58:25.882046+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jph2 has been classified as Red List (Low Evidence).",
"entity_name": "JPH2",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:55:55.684075+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NODAL as ready",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:55:55.675480+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:55:41.570103+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NODAL were changed from to Heterotaxy, visceral, 5 (MIM#270100)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:55:16.409395+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NODAL were set to ",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:54:51.937077+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NODAL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:54:33.727410+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NODAL as Red List (low evidence)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:54:33.718181+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:54:14.442514+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NODAL.",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:54:00.833841+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NODAL: Rating: RED; Mode of pathogenicity: None; Publications: 9354794, 19064609; Phenotypes: Heterotaxy, visceral, 5 (MIM#270100); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:53:04.402422+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NODAL as ready",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:53:04.393951+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:53:02.013172+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NODAL were changed from to Heterotaxy, visceral, 5 (MIM#270100)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:52:32.760084+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NODAL were set to ",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:52:03.743687+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NODAL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:43:08.120960+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NODAL as Red List (low evidence)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:43:08.107844+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:42:37.310556+10:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NODAL: Rating: RED; Mode of pathogenicity: None; Publications: 9354794, 19064609; Phenotypes: Heterotaxy, visceral, 5 (MIM#270100); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:41:37.902639+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NODAL as ready",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:41:37.891876+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:41:35.213758+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NODAL were changed from to Heterotaxy, visceral, 5 (MIM#270100)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:41:03.401274+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NODAL were set to ",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:40:39.947929+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NODAL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:40:05.879611+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NODAL as Red List (low evidence)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:40:05.870813+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:39:36.876745+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NODAL: Rating: RED; Mode of pathogenicity: None; Publications: 9354794, 19064609; Phenotypes: Heterotaxy, visceral, 5 (MIM#270100); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:38:48.049364+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NODAL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:34:22.118496+10:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NODAL as ready",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:34:22.105273+10:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:33:45.394806+10:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NODAL as Red List (low evidence)",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:33:45.385999+10:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nodal has been classified as Red List (Low Evidence).",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2020-05-11T20:33:09.092446+10:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NODAL.",
"entity_name": "NODAL",
"entity_type": "gene"
}
]
}