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{
"count": 220263,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2178",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2176",
"results": [
{
"created": "2019-11-17T17:24:59.390341+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN5A was added\ngene: SCN5A was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN5A was set to Unknown",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:59.301644+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN4B was added\ngene: SCN4B was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SCN4B was set to Unknown",
"entity_name": "SCN4B",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:59.217141+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNQ1 was added\ngene: KCNQ1 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNQ1 was set to Unknown",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:59.129364+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNJ5 was added\ngene: KCNJ5 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ5 was set to Unknown",
"entity_name": "KCNJ5",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:59.043559+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNJ2 was added\ngene: KCNJ2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ2 was set to Unknown",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.949778+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNH2 was added\ngene: KCNH2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNH2 was set to Unknown",
"entity_name": "KCNH2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.853870+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNE2 was added\ngene: KCNE2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNE2 was set to Unknown",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.756246+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNE1 was added\ngene: KCNE1 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNE1 was set to Unknown",
"entity_name": "KCNE1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.638119+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CAV3 was added\ngene: CAV3 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAV3 was set to Unknown",
"entity_name": "CAV3",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.528678+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNA1C was added\ngene: CACNA1C was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNA1C was set to Unknown",
"entity_name": "CACNA1C",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.424429+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ANK2 was added\ngene: ANK2 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ANK2 was set to Unknown",
"entity_name": "ANK2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.317216+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AKAP9 was added\ngene: AKAP9 was added to Long QT syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AKAP9 was set to Unknown",
"entity_name": "AKAP9",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:58.247126+11:00",
"panel_name": "Long QT syndrome_VCGS",
"panel_id": 131,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Long QT syndrome_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T17:24:46.624572+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZMPSTE24 was added\ngene: ZMPSTE24 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZMPSTE24 was set to Unknown",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.545118+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WRN was added\ngene: WRN was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WRN was set to Unknown",
"entity_name": "WRN",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.472000+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SPRTN was added\ngene: SPRTN was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPRTN was set to Unknown",
"entity_name": "SPRTN",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.398567+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSMB8 was added\ngene: PSMB8 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PSMB8 was set to Unknown",
"entity_name": "PSMB8",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.320557+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PPARG was added\ngene: PPARG was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PPARG was set to Unknown",
"entity_name": "PPARG",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.248019+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: POLD1 was added\ngene: POLD1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: POLD1 was set to Unknown",
"entity_name": "POLD1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.174970+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLIN1 was added\ngene: PLIN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PLIN1 was set to Unknown",
"entity_name": "PLIN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.101106+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIK3R1 was added\ngene: PIK3R1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PIK3R1 was set to Unknown",
"entity_name": "PIK3R1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:46.030203+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PCYT1A was added\ngene: PCYT1A was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PCYT1A was set to Unknown",
"entity_name": "PCYT1A",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.957831+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LMNB2 was added\ngene: LMNB2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LMNB2 was set to Unknown",
"entity_name": "LMNB2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.883880+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LMNA was added\ngene: LMNA was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LMNA was set to Unknown",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.809858+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LIPE was added\ngene: LIPE was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LIPE was set to Unknown",
"entity_name": "LIPE",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.738148+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNJ6 was added\ngene: KCNJ6 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ6 was set to Unknown",
"entity_name": "KCNJ6",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.668093+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FBN1 was added\ngene: FBN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FBN1 was set to Unknown",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.595665+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ERCC8 was added\ngene: ERCC8 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ERCC8 was set to Unknown",
"entity_name": "ERCC8",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.521423+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ERCC6 was added\ngene: ERCC6 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ERCC6 was set to Unknown",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.445164+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CIDEC was added\ngene: CIDEC was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CIDEC was set to Unknown",
"entity_name": "CIDEC",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.377863+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CAVIN1 was added\ngene: CAVIN1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAVIN1 was set to Unknown",
"entity_name": "CAVIN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.308005+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CAV1 was added\ngene: CAV1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAV1 was set to Unknown",
"entity_name": "CAV1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:45.229671+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BSCL2 was added\ngene: BSCL2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BSCL2 was set to Unknown",
"entity_name": "BSCL2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:44.964609+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BLM was added\ngene: BLM was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BLM was set to Unknown",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:44.896810+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BANF1 was added\ngene: BANF1 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BANF1 was set to Unknown",
"entity_name": "BANF1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:44.830599+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AKT2 was added\ngene: AKT2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AKT2 was set to Unknown",
"entity_name": "AKT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:44.752771+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AGPAT2 was added\ngene: AGPAT2 was added to Lipodystrophy / Lipoatrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AGPAT2 was set to Unknown",
"entity_name": "AGPAT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:44.708647+11:00",
"panel_name": "Lipodystrophy / Lipoatrophy_VCGS",
"panel_id": 130,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Lipodystrophy / Lipoatrophy_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T17:24:24.285026+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZIC4 was added\ngene: ZIC4 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZIC4 was set to Unknown",
"entity_name": "ZIC4",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:24.212201+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZIC1 was added\ngene: ZIC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZIC1 was set to Unknown",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:24.139314+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WNT1 was added\ngene: WNT1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WNT1 was set to Unknown",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:24.004532+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR81 was added\ngene: WDR81 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR81 was set to Unknown",
"entity_name": "WDR81",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.925628+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VLDLR was added\ngene: VLDLR was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VLDLR was set to Unknown",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.852573+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTC21B was added\ngene: TTC21B was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TTC21B was set to Unknown",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.778650+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM67 was added\ngene: TMEM67 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM67 was set to Unknown",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.700235+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM237 was added\ngene: TMEM237 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM237 was set to Unknown",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.624030+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM231 was added\ngene: TMEM231 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM231 was set to Unknown",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.552289+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM216 was added\ngene: TMEM216 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM216 was set to Unknown",
"entity_name": "TMEM216",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.475478+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM138 was added\ngene: TMEM138 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM138 was set to Unknown",
"entity_name": "TMEM138",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.397248+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCTN3 was added\ngene: TCTN3 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN3 was set to Unknown",
"entity_name": "TCTN3",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.327894+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCTN2 was added\ngene: TCTN2 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN2 was set to Unknown",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.258877+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCTN1 was added\ngene: TCTN1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN1 was set to Unknown",
"entity_name": "TCTN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.187841+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SUFU was added\ngene: SUFU was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SUFU was set to Unknown",
"entity_name": "SUFU",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.106921+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RPGRIP1L was added\ngene: RPGRIP1L was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RPGRIP1L was set to Unknown",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:23.018163+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PDE6D was added\ngene: PDE6D was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PDE6D was set to Unknown",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.947920+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OFD1 was added\ngene: OFD1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OFD1 was set to Unknown",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.872885+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NPHP3 was added\ngene: NPHP3 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NPHP3 was set to Unknown",
"entity_name": "NPHP3",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.795363+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NPHP1 was added\ngene: NPHP1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NPHP1 was set to Unknown",
"entity_name": "NPHP1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.724392+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NID1 was added\ngene: NID1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NID1 was set to Unknown",
"entity_name": "NID1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.649071+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MKS1 was added\ngene: MKS1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MKS1 was set to Unknown",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.575740+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LAMC1 was added\ngene: LAMC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LAMC1 was set to Unknown",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.503070+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF7 was added\ngene: KIF7 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIF7 was set to Unknown",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.432513+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: INPP5E was added\ngene: INPP5E was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: INPP5E was set to Unknown",
"entity_name": "INPP5E",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.359662+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FOXC1 was added\ngene: FOXC1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FOXC1 was set to Unknown",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.289504+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CSPP1 was added\ngene: CSPP1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CSPP1 was set to Unknown",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.216723+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: C5orf42 was added\ngene: C5orf42 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: C5orf42 was set to Unknown",
"entity_name": "C5orf42",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.145584+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CEP41 was added\ngene: CEP41 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP41 was set to Unknown",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.076142+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CEP290 was added\ngene: CEP290 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CEP290 was set to Unknown",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:22.006591+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CC2D2A was added\ngene: CC2D2A was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CC2D2A was set to Unknown",
"entity_name": "CC2D2A",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.933101+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: B9D2 was added\ngene: B9D2 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: B9D2 was set to Unknown",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.864734+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: B9D1 was added\ngene: B9D1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: B9D1 was set to Unknown",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.793951+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARMC8 was added\ngene: ARMC8 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ARMC8 was set to Unknown",
"entity_name": "ARMC8",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.717927+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARL13B was added\ngene: ARL13B was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ARL13B was set to Unknown",
"entity_name": "ARL13B",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.642217+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AHI1 was added\ngene: AHI1 was added to Joubert syndrome and other cerebellar malformations_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AHI1 was set to Unknown",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:24:21.598958+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Joubert syndrome and other cerebellar malformations_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T17:22:07.729814+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: XK was added\ngene: XK was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: XK was set to Unknown",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.634363+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WT1 was added\ngene: WT1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WT1 was set to Unknown",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.543515+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VPS13A was added\ngene: VPS13A was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VPS13A was set to Unknown",
"entity_name": "VPS13A",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.458788+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VHL was added\ngene: VHL was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VHL was set to Unknown",
"entity_name": "VHL",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.372530+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VCP was added\ngene: VCP was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VCP was set to Unknown",
"entity_name": "VCP",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.285437+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VAPB was added\ngene: VAPB was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VAPB was set to Unknown",
"entity_name": "VAPB",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.196346+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: UCHL1 was added\ngene: UCHL1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: UCHL1 was set to Unknown",
"entity_name": "UCHL1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.096909+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: UBQLN2 was added\ngene: UBQLN2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: UBQLN2 was set to Unknown",
"entity_name": "UBQLN2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:07.000207+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA4A was added\ngene: TUBA4A was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TUBA4A was set to Unknown",
"entity_name": "TUBA4A",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.915129+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTN was added\ngene: TTN was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TTN was set to Unknown",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.831066+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TSC2 was added\ngene: TSC2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSC2 was set to Unknown",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.746232+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TSC1 was added\ngene: TSC1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSC1 was set to Unknown",
"entity_name": "TSC1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.658282+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TPM1 was added\ngene: TPM1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TPM1 was set to Unknown",
"entity_name": "TPM1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.564942+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TP53 was added\ngene: TP53 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TP53 was set to Unknown",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.467989+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNNT2 was added\ngene: TNNT2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TNNT2 was set to Unknown",
"entity_name": "TNNT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.365392+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNNI3 was added\ngene: TNNI3 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TNNI3 was set to Unknown",
"entity_name": "TNNI3",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.276995+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM43 was added\ngene: TMEM43 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM43 was set to Unknown",
"entity_name": "TMEM43",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:06.185433+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TH was added\ngene: TH was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TH was set to Unknown",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.987464+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TGFBR2 was added\ngene: TGFBR2 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TGFBR2 was set to Unknown",
"entity_name": "TGFBR2",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.897856+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TGFBR1 was added\ngene: TGFBR1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TGFBR1 was set to Unknown",
"entity_name": "TGFBR1",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.803392+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TARDBP was added\ngene: TARDBP was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TARDBP was set to Unknown",
"entity_name": "TARDBP",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.718144+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STK11 was added\ngene: STK11 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STK11 was set to Unknown",
"entity_name": "STK11",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.624793+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SPG11 was added\ngene: SPG11 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPG11 was set to Unknown",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.529922+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SPART was added\ngene: SPART was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SPART was set to Unknown",
"entity_name": "SPART",
"entity_type": "gene"
},
{
"created": "2019-11-17T17:22:05.441622+11:00",
"panel_name": "Incidentalome_VCGS",
"panel_id": 126,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SORL1 was added\ngene: SORL1 was added to Incidentalome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SORL1 was set to Unknown",
"entity_name": "SORL1",
"entity_type": "gene"
}
]
}