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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1671",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1669",
"results": [
{
"created": "2020-08-16T13:54:54.807167+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTPRJ was added\ngene: PTPRJ was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: PTPRJ was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PTPRJ were set to 30591527\nPhenotypes for gene: PTPRJ were set to Thrombocytopaenia\nReview for gene: PTPRJ was set to AMBER\nAdded comment: Two siblings reported with nonsyndromic thrombocytopenia characterised by spontaneous bleeding, small-sized platelets, and impaired platelet responses to the GPVI agonists collagen and convulxin. Supportive zebrafish model. \nSources: Expert list",
"entity_name": "PTPRJ",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:54:45.098838+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTPRJ were changed from Thrombocytopania to Thrombocytopaenia",
"entity_name": "PTPRJ",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:53:44.934123+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PTPRJ as Amber List (moderate evidence)",
"entity_name": "PTPRJ",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:53:44.926132+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptprj has been classified as Amber List (Moderate Evidence).",
"entity_name": "PTPRJ",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:53:22.905715+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTPRJ was added\ngene: PTPRJ was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PTPRJ was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PTPRJ were set to 30591527\nPhenotypes for gene: PTPRJ were set to Thrombocytopania\nReview for gene: PTPRJ was set to AMBER\nAdded comment: Two siblings reported with nonsyndromic thrombocytopenia characterised by spontaneous bleeding, small-sized platelets, and impaired platelet responses to the GPVI agonists collagen and convulxin. Supportive zebrafish model. \nSources: Expert list",
"entity_name": "PTPRJ",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:49:10.824644+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTPN11 as ready",
"entity_name": "PTPN11",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:49:10.816527+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptpn11 has been classified as Green List (High Evidence).",
"entity_name": "PTPN11",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:49:06.598020+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PTPN11 as Green List (high evidence)",
"entity_name": "PTPN11",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:49:06.588595+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptpn11 has been classified as Green List (High Evidence).",
"entity_name": "PTPN11",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:48:40.345619+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTPN11 was added\ngene: PTPN11 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PTPN11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PTPN11 were set to Noonan syndrome 1, MIM#\t163950\nMode of pathogenicity for gene: PTPN11 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments\nReview for gene: PTPN11 was set to GREEN\nAdded comment: Thrombocytopaenia and bleeding tendency are common features of PTPN11-associated Noonan syndrome. \nSources: Expert list",
"entity_name": "PTPN11",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:48.564373+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTGS1 as ready",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:48.554043+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:40.907494+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PTGS1 as Amber List (moderate evidence)",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:40.889641+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:24.743765+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTGS1 was added\ngene: PTGS1 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: PTGS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PTGS1 were set to 32299908; 11442478; 27629384; 8562397\nPhenotypes for gene: PTGS1 were set to Platelet dysfunction; bleeding\nReview for gene: PTGS1 was set to AMBER\nAdded comment: Single molecularly characterised family reported. However, note at least two previous older reports where deficiency was identified at protein rather than gene level. \nSources: Expert list",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:44:17.622670+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTGS1 were set to 32299908; 11442478; 27629384 8562397",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:42:25.498570+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTGS1 as ready",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:42:25.488064+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:42:20.841647+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PTGS1 as Amber List (moderate evidence)",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:42:20.831733+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgs1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:41:51.347465+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PTGS1: Changed publications: 32299908, 11442478, 27629384, 8562397",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:41:44.052060+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTGS1 was added\ngene: PTGS1 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PTGS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PTGS1 were set to 32299908; 11442478; 27629384 8562397\nPhenotypes for gene: PTGS1 were set to Platelet dysfunction; bleeding\nReview for gene: PTGS1 was set to AMBER\nAdded comment: Single molecularly characterised family reported. However, note at least two previous older reports where deficiency was identified at protein rather than gene level. \nSources: Expert list",
"entity_name": "PTGS1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:32:22.073390+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKG1 as ready",
"entity_name": "PRKG1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:32:22.062035+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkg1 has been classified as Green List (High Evidence).",
"entity_name": "PRKG1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:32:19.048821+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKG1 were changed from to Aortic aneurysm, familial thoracic 8, MIM# 615436",
"entity_name": "PRKG1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:31:53.107605+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRKG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKG1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:31:30.435063+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRKG1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 8, MIM# 615436; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKG1",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:29:59.147472+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKACG as ready",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:29:59.136172+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkacg has been classified as Red List (Low Evidence).",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:29:49.450452+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRKACG was added\ngene: PRKACG was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: PRKACG was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PRKACG were set to 25061177; 30819905\nPhenotypes for gene: PRKACG were set to Bleeding disorder, platelet-type, 19, MIM# 616176\nReview for gene: PRKACG was set to RED\nAdded comment: Single family reported only. A heterozygous VOUS reported in another individual in PMID 30819905 together with several other VOUS in same individual. \nSources: Expert list",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:28:29.665580+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKACG as ready",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:28:29.656889+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkacg has been classified as Red List (Low Evidence).",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:28:23.466460+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRKACG was added\ngene: PRKACG was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PRKACG was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PRKACG were set to 25061177; 30819905\nPhenotypes for gene: PRKACG were set to Bleeding disorder, platelet-type, 19, MIM# 616176\nReview for gene: PRKACG was set to RED\nAdded comment: Single family reported only. A heterozygous VOUS reported in another individual in PMID 30819905 together with several other VOUS in same individual. \nSources: Expert list",
"entity_name": "PRKACG",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:58.547445+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLAU as ready",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:58.539002+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plau has been classified as Green List (High Evidence).",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:45.855308+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PLAU as Green List (high evidence)",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:45.845249+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plau has been classified as Green List (High Evidence).",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:29.687646+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: PLAU.",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-16T13:19:19.350610+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLAU was added\ngene: PLAU was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: PLAU was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLAU were set to 20007542\nPhenotypes for gene: PLAU were set to Quebec platelet disorder, MIM#\t601709\nReview for gene: PLAU was set to GREEN\nAdded comment: Note this is a tandem 78kb duplication of the gene, multiple families reported. \nSources: Expert list",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T19:44:17.664569+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLAU as ready",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T19:44:17.653319+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plau has been classified as Green List (High Evidence).",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:54:01.181656+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PLAU as Green List (high evidence)",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:54:01.172042+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plau has been classified as Green List (High Evidence).",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:53:21.646429+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLAU was added\ngene: PLAU was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PLAU was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLAU were set to 20007542\nPhenotypes for gene: PLAU were set to Quebec platelet disorder, MIM#\t601709\nReview for gene: PLAU was set to GREEN\nAdded comment: Note this is a tandem 78kb duplication of the gene. \nSources: Expert list",
"entity_name": "PLAU",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:48:33.567716+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLA2G4A as ready",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:48:33.559192+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pla2g4a has been classified as Green List (High Evidence).",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:48:25.392914+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PLA2G4A as Green List (high evidence)",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:48:25.382911+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pla2g4a has been classified as Green List (High Evidence).",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:48:09.470464+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLA2G4A was added\ngene: PLA2G4A was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: PLA2G4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLA2G4A were set to 18451993; 25102815; 23268370\nPhenotypes for gene: PLA2G4A were set to Gastrointestinal ulceration, recurrent, with dysfunctional platelets, MIM# 618372\nReview for gene: PLA2G4A was set to GREEN\nAdded comment: At least three unrelated individuals reported. \nSources: Expert list",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:46:08.487018+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLA2G4A as ready",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:46:08.475867+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pla2g4a has been classified as Green List (High Evidence).",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:46:02.799840+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PLA2G4A as Green List (high evidence)",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:46:02.791982+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pla2g4a has been classified as Green List (High Evidence).",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:45:39.511880+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLA2G4A was added\ngene: PLA2G4A was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: PLA2G4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLA2G4A were set to 18451993; 25102815; 23268370\nPhenotypes for gene: PLA2G4A were set to Gastrointestinal ulceration, recurrent, with dysfunctional platelets, MIM#\t618372\nReview for gene: PLA2G4A was set to GREEN\nAdded comment: Sources: Expert list",
"entity_name": "PLA2G4A",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:42:53.710345+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOTCH1 as ready",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:42:53.699297+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: notch1 has been classified as Green List (High Evidence).",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:42:51.093801+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOTCH1 were changed from to Aortic aneurysm",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:42:24.775819+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOTCH1 were set to ",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:41:58.124100+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOTCH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:41:34.581831+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NOTCH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 16729972, 26820064, 16025100, 25963545; Phenotypes: Aortic aneurysm; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NOTCH1",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:39:12.725688+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NBEAL2 were set to ",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:38:48.873135+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: NBEAL2: Changed publications: 21765412, 21765411, 21765413; Changed phenotypes: Gray platelet syndrome, MIM# 139090",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:37:26.555544+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBEAL2 as ready",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:37:26.544863+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbeal2 has been classified as Green List (High Evidence).",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:37:20.970988+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NBEAL2 as Green List (high evidence)",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:37:20.961389+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbeal2 has been classified as Green List (High Evidence).",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:36:51.138144+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NBEAL2 was added\ngene: NBEAL2 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: NBEAL2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: NBEAL2 were set to Gray platelet syndrome, MIM#\t139090\nReview for gene: NBEAL2 was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list",
"entity_name": "NBEAL2",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:13:27.027085+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYLK as ready",
"entity_name": "MYLK",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:13:27.013500+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mylk has been classified as Green List (High Evidence).",
"entity_name": "MYLK",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:13:24.714815+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYLK were changed from to Aortic aneurysm, familial thoracic 7, MIM# 613780",
"entity_name": "MYLK",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:12:58.749411+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYLK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYLK",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:12:30.553453+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYLK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 7, MIM# 613780; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYLK",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:10:42.041066+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH9 as ready",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:10:42.027309+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh9 has been classified as Green List (High Evidence).",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:10:35.742256+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MYH9 as Green List (high evidence)",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:10:35.732181+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh9 has been classified as Green List (High Evidence).",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:10:07.624821+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYH9 was added\ngene: MYH9 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: MYH9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MYH9 were set to Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss, MIM#\t155100\nReview for gene: MYH9 was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:08:07.582918+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH11 as ready",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:08:07.570498+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh11 has been classified as Green List (High Evidence).",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:08:04.751842+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYH11 were changed from to Aortic aneurysm, familial thoracic 4, MIM# 132900",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:07:42.264925+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYH11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:07:19.702821+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYH11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 4, MIM# 132900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:05:20.756036+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPL as ready",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:05:20.745400+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpl has been classified as Green List (High Evidence).",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:05:10.631348+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MPL as Green List (high evidence)",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:05:10.621864+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpl has been classified as Green List (High Evidence).",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2020-08-15T18:04:48.752743+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MPL was added\ngene: MPL was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: MPL was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MPL were set to 11133753\nPhenotypes for gene: MPL were set to Thrombocytopenia, congenital amegakaryocytic, MIM#\t604498\nReview for gene: MPL was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:18:58.330747+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPIG6B as ready",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:18:58.319410+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpig6b has been classified as Green List (High Evidence).",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:18:50.466882+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MPIG6B as Green List (high evidence)",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:18:50.457037+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpig6b has been classified as Green List (High Evidence).",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:18:33.809270+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MPIG6B was added\ngene: MPIG6B was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MPIG6B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MPIG6B were set to 31276734; 29898956; 27743390\nPhenotypes for gene: MPIG6B were set to Thrombocytopenia, anemia, and myelofibrosis, MIM#\t617441\nReview for gene: MPIG6B was set to GREEN\nAdded comment: Six families reported. \nSources: Expert list",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:17:02.113410+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPIG6B as ready",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:17:02.086404+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpig6b has been classified as Green List (High Evidence).",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:16:50.601506+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MPIG6B as Green List (high evidence)",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:16:50.593497+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpig6b has been classified as Green List (High Evidence).",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T17:16:27.139672+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MPIG6B was added\ngene: MPIG6B was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: MPIG6B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MPIG6B were set to 31276734; 29898956; 27743390\nPhenotypes for gene: MPIG6B were set to Thrombocytopenia, anemia, and myelofibrosis, MIM#\t617441\nReview for gene: MPIG6B was set to GREEN\nAdded comment: Six families reported. \nSources: Expert list",
"entity_name": "MPIG6B",
"entity_type": "gene"
},
{
"created": "2020-08-15T16:40:15.462333+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MFAP5 as ready",
"entity_name": "MFAP5",
"entity_type": "gene"
},
{
"created": "2020-08-15T16:40:15.453658+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mfap5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MFAP5",
"entity_type": "gene"
},
{
"created": "2020-08-15T16:40:12.502054+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MFAP5 were changed from to Aortic aneurysm, familial thoracic MIM# 616166",
"entity_name": "MFAP5",
"entity_type": "gene"
}
]
}