{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2107","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}