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{
"count": 220437,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1509",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1507",
"results": [
{
"created": "2020-11-09T16:41:59.296106+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BRAF was added\ngene: BRAF was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRAF was set to Unknown",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.254948+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BMPR1A was added\ngene: BMPR1A was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BMPR1A was set to Unknown",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.212580+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BIRC3 was added\ngene: BIRC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BIRC3 was set to Unknown",
"entity_name": "BIRC3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.170669+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BCR was added\ngene: BCR was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCR was set to Unknown",
"entity_name": "BCR",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.129155+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BCL6 was added\ngene: BCL6 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCL6 was set to Unknown",
"entity_name": "BCL6",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.086882+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BCL2 was added\ngene: BCL2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BCL2 was set to Unknown",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.045563+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BAP1 was added\ngene: BAP1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BAP1 was set to Unknown",
"entity_name": "BAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:59.003473+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATM was added\ngene: ATM was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ATM was set to Unknown",
"entity_name": "ATM",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.963234+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARL11 was added\ngene: ARL11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ARL11 was set to Unknown",
"entity_name": "ARL11",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.922630+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: APC was added\ngene: APC was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: APC was set to Unknown",
"entity_name": "APC",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.880911+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ABL1 was added\ngene: ABL1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ABL1 was set to Unknown",
"entity_name": "ABL1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.828823+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNA1S was added\ngene: CACNA1S was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CACNA1S was set to Unknown",
"entity_name": "CACNA1S",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.785820+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RYR1 was added\ngene: RYR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RYR1 was set to Unknown",
"entity_name": "RYR1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.738804+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TGFBR1 was added\ngene: TGFBR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TGFBR1 was set to Unknown",
"entity_name": "TGFBR1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.697311+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SMAD3 was added\ngene: SMAD3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SMAD3 was set to Unknown",
"entity_name": "SMAD3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.656471+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYH11 was added\ngene: MYH11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYH11 was set to Unknown",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.613270+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FBN1 was added\ngene: FBN1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: FBN1 was set to Unknown",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.574238+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL3A1 was added\ngene: COL3A1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: COL3A1 was set to Unknown",
"entity_name": "COL3A1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.534512+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTA2 was added\ngene: ACTA2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ACTA2 was set to Unknown",
"entity_name": "ACTA2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.495329+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TPM1 was added\ngene: TPM1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TPM1 was set to Unknown",
"entity_name": "TPM1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.456036+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNNT2 was added\ngene: TNNT2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TNNT2 was set to Unknown",
"entity_name": "TNNT2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.414515+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNNI3 was added\ngene: TNNI3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TNNI3 was set to Unknown",
"entity_name": "TNNI3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.373234+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM43 was added\ngene: TMEM43 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TMEM43 was set to Unknown",
"entity_name": "TMEM43",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.334265+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN5A was added\ngene: SCN5A was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SCN5A was set to Unknown",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.295873+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RYR2 was added\ngene: RYR2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RYR2 was set to Unknown",
"entity_name": "RYR2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.257996+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRKAG2 was added\ngene: PRKAG2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PRKAG2 was set to Unknown",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.220281+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PKP2 was added\ngene: PKP2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PKP2 was set to Unknown",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.182043+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LMNA was added\ngene: LMNA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: LMNA was set to Unknown",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.143969+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYH7 was added\ngene: MYH7 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYH7 was set to Unknown",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.105190+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYL3 was added\ngene: MYL3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYL3 was set to Unknown",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.067204+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYL2 was added\ngene: MYL2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYL2 was set to Unknown",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:58.029450+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYBPC3 was added\ngene: MYBPC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MYBPC3 was set to Unknown",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.991909+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNH2 was added\ngene: KCNH2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: KCNH2 was set to Unknown",
"entity_name": "KCNH2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.955064+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNQ1 was added\ngene: KCNQ1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: KCNQ1 was set to Unknown",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.917076+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GLA was added\ngene: GLA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GLA was set to Unknown",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.880011+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DSP was added\ngene: DSP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSP was set to Unknown",
"entity_name": "DSP",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.839053+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DSG2 was added\ngene: DSG2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSG2 was set to Unknown",
"entity_name": "DSG2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.775067+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DSC2 was added\ngene: DSC2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: DSC2 was set to Unknown",
"entity_name": "DSC2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.731750+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTC1 was added\ngene: ACTC1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ACTC1 was set to Unknown",
"entity_name": "ACTC1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.693647+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WT1 was added\ngene: WT1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: WT1 was set to Unknown",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.651904+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STK11 was added\ngene: STK11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: STK11 was set to Unknown",
"entity_name": "STK11",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.610270+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RB1 was added\ngene: RB1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: RB1 was set to Unknown",
"entity_name": "RB1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.568244+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BRCA2 was added\ngene: BRCA2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRCA2 was set to Unknown",
"entity_name": "BRCA2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.530339+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BRCA1 was added\ngene: BRCA1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: BRCA1 was set to Unknown",
"entity_name": "BRCA1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.492574+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP7B was added\ngene: ATP7B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ATP7B was set to Unknown",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.447517+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GBA was added\ngene: GBA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GBA was set to Unknown",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.403921+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SNCB was added\ngene: SNCB was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SNCB was set to Unknown",
"entity_name": "SNCB",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.364385+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SNCA was added\ngene: SNCA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SNCA was set to Unknown",
"entity_name": "SNCA",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.323091+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TARDBP was added\ngene: TARDBP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TARDBP was set to Unknown",
"entity_name": "TARDBP",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.284297+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CHMP2B was added\ngene: CHMP2B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CHMP2B was set to Unknown",
"entity_name": "CHMP2B",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.245744+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: C9orf72 was added\ngene: C9orf72 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: C9orf72 was set to Unknown",
"entity_name": "C9orf72",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.205149+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GRN was added\ngene: GRN was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: GRN was set to Unknown",
"entity_name": "GRN",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.164719+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MAPT was added\ngene: MAPT was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: MAPT was set to Unknown",
"entity_name": "MAPT",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.126955+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ITM2B was added\ngene: ITM2B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ITM2B was set to Unknown",
"entity_name": "ITM2B",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.085700+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CST3 was added\ngene: CST3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: CST3 was set to Unknown",
"entity_name": "CST3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.047319+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NOTCH3 was added\ngene: NOTCH3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: NOTCH3 was set to Unknown",
"entity_name": "NOTCH3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:57.011065+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SQSTM1 was added\ngene: SQSTM1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SQSTM1 was set to Unknown",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.973503+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VCP was added\ngene: VCP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: VCP was set to Unknown",
"entity_name": "VCP",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.936051+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TYROBP was added\ngene: TYROBP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TYROBP was set to Unknown",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.899455+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TREM2 was added\ngene: TREM2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TREM2 was set to Unknown",
"entity_name": "TREM2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.853031+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSEN2 was added\ngene: PSEN2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PSEN2 was set to Unknown",
"entity_name": "PSEN2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.812414+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSEN1 was added\ngene: PSEN1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: PSEN1 was set to Unknown",
"entity_name": "PSEN1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.770279+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: APP was added\ngene: APP was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: APP was set to Unknown",
"entity_name": "APP",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:41:56.743645+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Incidentalome_NSW",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-11-07T15:31:28.703046+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATAD3A as ready",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:31:28.694147+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad3a has been classified as Green List (High Evidence).",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:31:26.373719+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATAD3A were changed from 618810 to Harel-Yoon syndrome, MIM# 617183; Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal (PHRINL SYNDROME), MIM# 618810; perinatal cardiomyopathy; cataracts; corneal clouding",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:31:14.710526+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATAD3A were set to PMID: 32004445",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:30:56.344827+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: ATAD3A.",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:30:50.583984+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATAD3A as Green List (high evidence)",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:30:50.574453+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad3a has been classified as Green List (High Evidence).",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:29:48.307598+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.38",
"user_name": "John Christodoulou",
"item_type": "entity",
"text": "reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 32004445, PMID: 27640307, PMID: 28549128, also Frazier et al, Med (in press); Phenotypes: Harel-Yoon syndrome, MIM# 617183, Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal (PHRINL SYNDROME), MIM# 618810, perinatal cardiomyopathy, cataracts, corneal clouding; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:29:37.432027+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACAD9 as ready",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:29:37.423362+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: acad9 has been classified as Green List (High Evidence).",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:29:30.229167+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ACAD9 were changed from to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:29:12.666132+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5337",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ACAD9 were set to ",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:28:54.724246+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5336",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:28:36.712718+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5335",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:27:21.964993+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5335",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CNP were changed from Hypomyelinating leukodystrophy to Leukodystrophy, hypomyelinating, 20, MIM# 619071",
"entity_name": "CNP",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:26:59.865157+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5334",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CNP: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukodystrophy, hypomyelinating, 20, MIM# 619071; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CNP",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:26:38.773455+11:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CNP were changed from Hypomyelinating leukodystrophy to Leukodystrophy, hypomyelinating, 20, MIM# 619071",
"entity_name": "CNP",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:26:20.922182+11:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CNP: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukodystrophy, hypomyelinating, 20, MIM# 619071; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CNP",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:14:56.205754+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.38",
"user_name": "John Christodoulou",
"item_type": "entity",
"text": "gene: ATAD3A was added\ngene: ATAD3A was added to Cardiomyopathy_Paediatric. Sources: Literature,Expert Review\nMode of inheritance for gene: ATAD3A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ATAD3A were set to PMID: 32004445\nPhenotypes for gene: ATAD3A were set to 618810\nPenetrance for gene: ATAD3A were set to Complete",
"entity_name": "ATAD3A",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:00:02.255159+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.553",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACAD9 as ready",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T15:00:02.235095+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.553",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: acad9 has been classified as Green List (High Evidence).",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:59:59.457122+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.553",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ACAD9 were changed from to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:59:30.353856+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.552",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ACAD9 were set to ",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:59:01.420248+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.551",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:58:32.953758+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.550",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:27:16.419688+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACAD9 as ready",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:27:16.409818+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: acad9 has been classified as Green List (High Evidence).",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:26:56.845591+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ACAD9 were changed from to Mitochondrial complex I deficiency, nuclear type 20 MIM#611126",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:26:29.807550+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ACAD9 were set to ",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:26:02.217661+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ACAD9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-07T14:25:27.945085+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ACAD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30025539; Phenotypes: Mitochondrial complex I deficiency, nuclear type 20 MIM#611126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2020-11-06T16:11:42.422916+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.47",
"user_name": "Sarah Righetti",
"item_type": "entity",
"text": "reviewed gene: NEXMIF: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 98, MIM #300912; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "NEXMIF",
"entity_type": "gene"
},
{
"created": "2020-11-06T16:06:06.433198+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.47",
"user_name": "Sarah Righetti",
"item_type": "entity",
"text": "reviewed gene: CLCN4: Rating: GREEN; Mode of pathogenicity: None; Publications: 27550844; Phenotypes: Raynaud-Claes syndrome, MIM #300114; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "CLCN4",
"entity_type": "gene"
},
{
"created": "2020-11-06T16:02:57.558091+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.47",
"user_name": "Sarah Righetti",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "NYX",
"entity_type": "gene"
},
{
"created": "2020-11-06T16:02:53.668950+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.47",
"user_name": "Sarah Righetti",
"item_type": "entity",
"text": "edited their review of gene: NYX: Added comment: Clinical summary: Function of rods disrupted - difficulty seeing in low light. Other vision problems including reduced acuity (20/30 to 20/200) which is considered mild-moderate visual impairment or reduced-low vision. 20/40 is Australian legal driving limit. Myopia - can range from low to high. May have nystagmus/strabismus. Color vision not affected. Non-progressive, present at birth.\r\n\r\nSevere end of phenoypic spectrum meets MM criteria for inclusion - GREEN; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "NYX",
"entity_type": "gene"
},
{
"created": "2020-11-06T16:02:32.042730+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.47",
"user_name": "Sarah Righetti",
"item_type": "entity",
"text": "reviewed gene: NYX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1A, X-linked, MIM #310500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NYX",
"entity_type": "gene"
}
]
}