HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2107",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2105",
"results": [
{
"created": "2019-11-18T14:35:14.856794+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: MRE11 was added\ngene: MRE11 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: MRE11 was set to Unknown\nPublications for gene: MRE11 were set to PMID: 30234181",
"entity_name": "MRE11",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.785201+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: MGMT was added\ngene: MGMT was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: MGMT was set to Unknown",
"entity_name": "MGMT",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.715559+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCM was added\ngene: FANCM was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: FANCM was set to Unknown\nPublications for gene: FANCM were set to PMID: 16912188",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.645872+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCL was added\ngene: FANCL was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCL was set to Unknown\nPublications for gene: FANCL were set to PMID: 30234181",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.576584+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCG was added\ngene: FANCG was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCG was set to Unknown\nPublications for gene: FANCG were set to PMID: 30234181",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.506722+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCF was added\ngene: FANCF was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCF was set to Unknown\nPublications for gene: FANCF were set to PMID: 30234181",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.434408+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCE was added\ngene: FANCE was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: FANCE was set to Unknown",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.364711+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCD2 was added\ngene: FANCD2 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCD2 was set to Unknown\nPublications for gene: FANCD2 were set to PMID: 30234181",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.295208+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCC was added\ngene: FANCC was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCC was set to Unknown\nPublications for gene: FANCC were set to PMID: 30234181",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.222382+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FANCA was added\ngene: FANCA was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: FANCA was set to Unknown\nPublications for gene: FANCA were set to PMID: 30234181",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.152338+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FAN1 was added\ngene: FAN1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: FAN1 was set to Unknown",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.084099+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: FAAP20 was added\ngene: FAAP20 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: FAAP20 was set to Unknown",
"entity_name": "FAAP20",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:14.013781+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: CHEK2 was added\ngene: CHEK2 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CHEK2 was set to Unknown\nPublications for gene: CHEK2 were set to PMID: 30234181",
"entity_name": "CHEK2",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.941357+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: CHEK1 was added\ngene: CHEK1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CHEK1 was set to Unknown\nPublications for gene: CHEK1 were set to PMID: 30234181",
"entity_name": "CHEK1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.869820+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BRIP1 was added\ngene: BRIP1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: BRIP1 was set to Unknown\nPublications for gene: BRIP1 were set to PMID: 30234181",
"entity_name": "BRIP1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.797216+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BRCA2 was added\ngene: BRCA2 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: BRCA2 was set to Unknown\nPublications for gene: BRCA2 were set to PMID: 30234181",
"entity_name": "BRCA2",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.728261+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BRCA1 was added\ngene: BRCA1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: BRCA1 was set to Unknown\nPublications for gene: BRCA1 were set to PMID: 30234181",
"entity_name": "BRCA1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.659844+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BLM was added\ngene: BLM was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: BLM was set to Unknown\nPublications for gene: BLM were set to PMID: 30234181",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.592307+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BARD1 was added\ngene: BARD1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: BARD1 was set to Unknown\nPublications for gene: BARD1 were set to PMID: 30234181",
"entity_name": "BARD1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.522717+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: BAP1 was added\ngene: BAP1 was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: BAP1 was set to Unknown\nPublications for gene: BAP1 were set to PMID: 30234181",
"entity_name": "BAP1",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.454337+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: ATRX was added\ngene: ATRX was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ATRX was set to Unknown\nPublications for gene: ATRX were set to PMID: 30234181",
"entity_name": "ATRX",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.386579+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: ATR was added\ngene: ATR was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ATR was set to Unknown\nPublications for gene: ATR were set to PMID: 16912188",
"entity_name": "ATR",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.318187+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: ATM was added\ngene: ATM was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: ATM was set to Unknown\nPublications for gene: ATM were set to PMID: 30234181",
"entity_name": "ATM",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.249489+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "entity",
"text": "gene: ARID1A was added\ngene: ARID1A was added to Homologous recombination deficiency (HDR) for WTS report. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ARID1A was set to Unknown\nPublications for gene: ARID1A were set to PMID: 30234181",
"entity_name": "ARID1A",
"entity_type": "gene"
},
{
"created": "2019-11-18T14:35:13.207636+11:00",
"panel_name": "Homologous recombination deficiency (HDR) for WTS report",
"panel_id": 242,
"panel_version": "0.0",
"user_name": "Jacek Marzec",
"item_type": "panel",
"text": "Added panel Homologous recombination deficiency (HDR) for WTS report",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T13:00:24.946372+11:00",
"panel_name": "Immunological disorders_SuperPanel_VCGS",
"panel_id": 239,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added Panel Immunological disorders_SuperPanel_VCGS\nSet child panels to: Disorders of immune dysregulation_MelbourneGenomics_VCGS; Complement deficiencies_MelbourneGenomics_VCGS; Hereditary angioedema_MelbourneGenomics_VCGS; Hyper-IgE syndrome_MelbourneGenomics_VCGS; Mendelian susceptibility to Immune Disorders_MelbourneGenomics_VCGS; Defects of innate immunity_MelbourneGenomics_VCGS; Neutrophil defects_MelbourneGenomics_VCGS; Phagocyte defects_MelbourneGenomics_VCGS; Severe combined immunodeficiency (absent T, absent B cells)_MelbourneGenomics_VCGS; Severe combined immunodeficiency (absent T, present B cells)_MelbourneGenomics_VCGS; Susceptibility to fungal infections_MelbourneGenomics_VCGS; Susceptibility to viral infections_MelbourneGenomics_VCGS; Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_VCGS; Predominantly antibody deficiency_MelbourneGenomics_VCGS; Combined immunodeficiency_MelbourneGenomics_VCGS; Common Variable Immunodeficiency_MelbourneGenomics_VCGS\nSet panel types to: Superpanel",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T11:56:09.209283+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MECOM as Green List (high evidence)",
"entity_name": "MECOM",
"entity_type": "gene"
},
{
"created": "2019-11-18T11:56:09.197641+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mecom has been classified as Green List (High Evidence).",
"entity_name": "MECOM",
"entity_type": "gene"
},
{
"created": "2019-11-18T11:50:07.246723+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MECOM as ready",
"entity_name": "MECOM",
"entity_type": "gene"
},
{
"created": "2019-11-18T11:50:07.235705+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mecom has been classified as Red List (Low Evidence).",
"entity_name": "MECOM",
"entity_type": "gene"
},
{
"created": "2019-11-18T11:49:30.422028+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MECOM was added\ngene: MECOM was added to Bone Marrow Failure_VCGS. Sources: Expert Review\nMode of inheritance for gene: MECOM was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MECOM were set to 26581901\nPhenotypes for gene: MECOM were set to Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, MIM#616738\nReview for gene: MECOM was set to GREEN\ngene: MECOM was marked as current diagnostic\nAdded comment: Multiple affected families reported, syndromic features tend to cluster with mutations in a particular domain. Non-syndromic presentations well described. \nSources: Expert Review",
"entity_name": "MECOM",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:19:34.459559+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:18:46.772453+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS to Susceptibility to viral infections_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:17:33.608674+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MelbourneGenomics_VCGS",
"panel_id": 235,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS to Severe combined immunodeficiency (absent T, present B cells)_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:16:23.296352+11:00",
"panel_name": "Predominantly antibody deficiency_MelbourneGenomics_VCGS",
"panel_id": 222,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Predominantly antibody deficiency_MelbourneGenomics_AustralianGenomics_VCGS to Predominantly antibody deficiency_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:15:50.166917+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS to Phagocyte defects_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:13:11.164201+11:00",
"panel_name": "Hereditary angioedema_MelbourneGenomics_VCGS",
"panel_id": 226,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Hereditary angioedema_MGHA_AGHA_VCGS to Hereditary angioedema_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:10:32.760346+11:00",
"panel_name": "Disorders of immune dysregulation_MelbourneGenomics_VCGS",
"panel_id": 229,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Disorders of immune dysregulation_MGHA_AGHA_VCGS to Disorders of immune dysregulation_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:09:47.262792+11:00",
"panel_name": "Defects of innate immunity_MelbourneGenomics_VCGS",
"panel_id": 231,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Defects of innate immunity_MGHA_AGHA_VCGS to Defects of innate immunity_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:09:16.102577+11:00",
"panel_name": "Complement deficiencies_MelbourneGenomics_VCGS",
"panel_id": 224,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Complement deficiencies_MGHA_AGHA_VCGS to Complement deficiencies_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:08:13.197948+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Combined immunodeficiency_MelbourneGenomics_AustralianGenomics_VCGS to Combined immunodeficiency_MelbourneGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:03:31.708580+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRNT1 was added\ngene: TRNT1 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TRNT1 was set to Unknown",
"entity_name": "TRNT1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.628953+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNFRSF1A was added\ngene: TNFRSF1A was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TNFRSF1A was set to Unknown",
"entity_name": "TNFRSF1A",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.548583+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TNFAIP3 was added\ngene: TNFAIP3 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TNFAIP3 was set to Unknown",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.467000+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC29A3 was added\ngene: SLC29A3 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: SLC29A3 was set to Unknown",
"entity_name": "SLC29A3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.386543+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SH3BP2 was added\ngene: SH3BP2 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: SH3BP2 was set to Unknown",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.306417+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RBCK1 was added\ngene: RBCK1 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: RBCK1 was set to Unknown",
"entity_name": "RBCK1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.227243+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSTPIP1 was added\ngene: PSTPIP1 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PSTPIP1 was set to Unknown",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.146522+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSMB9 was added\ngene: PSMB9 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PSMB9 was set to Unknown",
"entity_name": "PSMB9",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:31.067844+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSMB8 was added\ngene: PSMB8 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PSMB8 was set to Unknown",
"entity_name": "PSMB8",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.987076+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSMB4 was added\ngene: PSMB4 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PSMB4 was set to Unknown",
"entity_name": "PSMB4",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.907726+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PSMA3 was added\ngene: PSMA3 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PSMA3 was set to Unknown",
"entity_name": "PSMA3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.830228+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLCG2 was added\ngene: PLCG2 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PLCG2 was set to Unknown",
"entity_name": "PLCG2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.751673+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OTULIN was added\ngene: OTULIN was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: OTULIN was set to Unknown",
"entity_name": "OTULIN",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.673294+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NOD2 was added\ngene: NOD2 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: NOD2 was set to Unknown",
"entity_name": "NOD2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.594054+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NLRP3 was added\ngene: NLRP3 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: NLRP3 was set to Unknown",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.516796+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NLRP12 was added\ngene: NLRP12 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: NLRP12 was set to Unknown",
"entity_name": "NLRP12",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.439573+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NLRC4 was added\ngene: NLRC4 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: NLRC4 was set to Unknown",
"entity_name": "NLRC4",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.360433+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MVK was added\ngene: MVK was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: MVK was set to Unknown",
"entity_name": "MVK",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.282985+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MEFV was added\ngene: MEFV was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: MEFV was set to Unknown",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.203504+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LPIN2 was added\ngene: LPIN2 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: LPIN2 was set to Unknown",
"entity_name": "LPIN2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:30.122467+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL36RN was added\ngene: IL36RN was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: IL36RN was set to Unknown",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.936946+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL1RN was added\ngene: IL1RN was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: IL1RN was set to Unknown",
"entity_name": "IL1RN",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.859859+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ELANE was added\ngene: ELANE was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: ELANE was set to Unknown",
"entity_name": "ELANE",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.780988+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COPA was added\ngene: COPA was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: COPA was set to Unknown",
"entity_name": "COPA",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.703793+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CARD14 was added\ngene: CARD14 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CARD14 was set to Unknown",
"entity_name": "CARD14",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.627105+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1S3 was added\ngene: AP1S3 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: AP1S3 was set to Unknown",
"entity_name": "AP1S3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.550265+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADAM17 was added\ngene: ADAM17 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: ADAM17 was set to Unknown",
"entity_name": "ADAM17",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.470787+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADA2 was added\ngene: ADA2 was added to Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: ADA2 was set to Unknown",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:29.419042+11:00",
"panel_name": "Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 238,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Systemic autoinflammatory disease, Periodic fever_MelbourneGenomics_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:03:08.968654+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: UNC93B1 was added\ngene: UNC93B1 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: UNC93B1 was set to Unknown",
"entity_name": "UNC93B1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.889755+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRAF3 was added\ngene: TRAF3 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TRAF3 was set to Unknown",
"entity_name": "TRAF3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.812070+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMC8 was added\ngene: TMC8 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TMC8 was set to Unknown",
"entity_name": "TMC8",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.734607+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMC6 was added\ngene: TMC6 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TMC6 was set to Unknown",
"entity_name": "TMC6",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.657282+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TLR3 was added\ngene: TLR3 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TLR3 was set to Unknown",
"entity_name": "TLR3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.580048+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TICAM1 was added\ngene: TICAM1 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TICAM1 was set to Unknown",
"entity_name": "TICAM1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.502760+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TBK1 was added\ngene: TBK1 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TBK1 was set to Unknown",
"entity_name": "TBK1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.424407+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STAT2 was added\ngene: STAT2 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: STAT2 was set to Unknown",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.347232+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STAT1 was added\ngene: STAT1 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: STAT1 was set to Unknown",
"entity_name": "STAT1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.270525+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IRF7 was added\ngene: IRF7 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: IRF7 was set to Unknown",
"entity_name": "IRF7",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.193589+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FCGR3A was added\ngene: FCGR3A was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: FCGR3A was set to Unknown",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.114429+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CXCR4 was added\ngene: CXCR4 was added to Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CXCR4 was set to Unknown",
"entity_name": "CXCR4",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:03:08.057841+11:00",
"panel_name": "Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 237,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Susceptibility to viral infections_MelbourneGenomics_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:02:47.406406+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTPRC was added\ngene: PTPRC was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: PTPRC was set to Unknown",
"entity_name": "PTPRC",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:47.330097+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: JAK3 was added\ngene: JAK3 was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: JAK3 was set to Unknown",
"entity_name": "JAK3",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:47.253527+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL7R was added\ngene: IL7R was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: IL7R was set to Unknown",
"entity_name": "IL7R",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:47.176675+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IL2RG was added\ngene: IL2RG was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: IL2RG was set to Unknown",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:47.099783+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CORO1A was added\ngene: CORO1A was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CORO1A was set to Unknown",
"entity_name": "CORO1A",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:47.022239+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD3E was added\ngene: CD3E was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CD3E was set to Unknown",
"entity_name": "CD3E",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:46.942911+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD3D was added\ngene: CD3D was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CD3D was set to Unknown",
"entity_name": "CD3D",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:46.864316+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD247 was added\ngene: CD247 was added to Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: CD247 was set to Unknown",
"entity_name": "CD247",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:46.814130+11:00",
"panel_name": "Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"panel_id": 235,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Severe combined immunodeficiency (absent T, present B cells)_MGHA_AGHA_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-18T10:02:25.699095+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WIPF1 was added\ngene: WIPF1 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: WIPF1 was set to Unknown",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.618386+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WAS was added\ngene: WAS was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: WAS was set to Unknown",
"entity_name": "WAS",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.536996+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VPS45 was added\ngene: VPS45 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: VPS45 was set to Unknown",
"entity_name": "VPS45",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.456999+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VPS13B was added\ngene: VPS13B was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: VPS13B was set to Unknown",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.377744+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: USB1 was added\ngene: USB1 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: USB1 was set to Unknown",
"entity_name": "USB1",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.296955+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TAZ was added\ngene: TAZ was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: TAZ was set to Unknown",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.217603+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC37A4 was added\ngene: SLC37A4 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: SLC37A4 was set to Unknown",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2019-11-18T10:02:25.139481+11:00",
"panel_name": "Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS",
"panel_id": 233,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC35C1 was added\ngene: SLC35C1 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship\nMode of inheritance for gene: SLC35C1 was set to Unknown",
"entity_name": "SLC35C1",
"entity_type": "gene"
}
]
}