{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1883","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1881","results":[{"created":"2020-04-05T15:40:18.109434+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MKL1 as Amber List (moderate evidence)","entity_name":"MKL1","entity_type":"gene"},{"created":"2020-04-05T15:40:18.095270+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mkl1 has been classified as Amber List (Moderate Evidence).","entity_name":"MKL1","entity_type":"gene"},{"created":"2020-04-05T15:39:47.366216+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MKL1 was added\ngene: MKL1 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: MKL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MKL1 were set to 32128589; 26224645\nPhenotypes for gene: MKL1 were set to Neutropaenia with combined immune deficiency\nReview for gene: MKL1 was set to AMBER\nAdded comment: Two unrelated families reported. \nSources: Expert list","entity_name":"MKL1","entity_type":"gene"},{"created":"2020-04-05T15:36:30.609432+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR1 were changed from Neutrpaenia; Poor wound healing; Severe stomatitis; Neutrophil nuclei herniate to Neutropaenia; Poor wound healing; Severe stomatitis; Neutrophil nuclei herniate","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:35:42.075634+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR1 as ready","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:35:42.062555+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr1 has been classified as Green List (High Evidence).","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:35:37.357554+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR1 were changed from  to Neutrpaenia; Poor wound healing; Severe stomatitis; Neutrophil nuclei herniate","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:34:37.221911+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WDR1 as Green List (high evidence)","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:34:37.208632+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr1 has been classified as Green List (High Evidence).","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:34:09.225483+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR1 was added\ngene: WDR1 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: WDR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WDR1 were set to 27994071; 27557945; 29751004\nReview for gene: WDR1 was set to GREEN\nAdded comment: Seven families reported with immunological phenotypes and bi-allelic variants in this gene, three of these had a predominantly phagocyte/neutrophil defects. \nSources: Expert list","entity_name":"WDR1","entity_type":"gene"},{"created":"2020-04-05T15:32:18.882252+10:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.15","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: CACNA1A as Green List (high evidence)","entity_name":"CACNA1A","entity_type":"gene"},{"created":"2020-04-05T15:32:18.868895+10:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.15","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: cacna1a has been classified as Green List (High Evidence).","entity_name":"CACNA1A","entity_type":"gene"},{"created":"2020-04-05T15:32:05.975845+10:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.14","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CACNA1A was added\ngene: CACNA1A was added to Dystonia - complex. Sources: Expert list\nMode of inheritance for gene: CACNA1A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: CACNA1A were set to 25468264; 23441182; 19232643; 18758887; 11344116\nPhenotypes for gene: CACNA1A were set to Episodic ataxia, type 2 MIM#108500; Spinocerebellar ataxia 6 MIM#183086\nReview for gene: CACNA1A was set to GREEN\nAdded comment: At least four families where dystonia is a feature of the condition (complex dystonia phenotype), and knockout mouse model also has dystonia as a feature of the phenotype. \nSources: Expert list","entity_name":"CACNA1A","entity_type":"gene"},{"created":"2020-04-05T15:26:31.584731+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAC2 as ready","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:26:31.571622+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rac2 has been classified as Green List (High Evidence).","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:22:10.994156+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAC2 were changed from  to Neutrophil immunodeficiency syndrome, MIM# 608203; Common variable immunodeficiency","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:21:44.454511+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAC2 were set to ","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:21:23.959599+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAC2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:20:46.089637+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 25512081; Phenotypes: Neutrophil immunodeficiency syndrome, MIM# 608203, Common variable immunodeficiency; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:18:59.488225+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RAC2: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAC2","entity_type":"gene"},{"created":"2020-04-05T15:15:39.487984+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SRP54 as ready","entity_name":"SRP54","entity_type":"gene"},{"created":"2020-04-05T15:15:39.475344+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: srp54 has been classified as Green List (High Evidence).","entity_name":"SRP54","entity_type":"gene"},{"created":"2020-04-05T15:15:35.351938+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SRP54 as Green List (high evidence)","entity_name":"SRP54","entity_type":"gene"},{"created":"2020-04-05T15:15:35.339046+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: srp54 has been classified as Green List (High Evidence).","entity_name":"SRP54","entity_type":"gene"},{"created":"2020-04-05T15:14:58.561307+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SRP54 was added\ngene: SRP54 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: SRP54 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SRP54 were set to 29914977; 28972538\nPhenotypes for gene: SRP54 were set to Neutropenia, severe congenital, 8, autosomal dominant, MIM#\t618752\nReview for gene: SRP54 was set to GREEN\nAdded comment: Over 25 individuals reported with Shwachman-Diamond like phenotype. \nSources: Expert list","entity_name":"SRP54","entity_type":"gene"},{"created":"2020-04-05T15:11:08.295654+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1954","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HYOU1 as ready","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:11:08.286526+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1954","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hyou1 has been classified as Red List (Low Evidence).","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:10:59.461577+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1954","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HYOU1 was added\ngene: HYOU1 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: HYOU1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HYOU1 were set to 27913302\nPhenotypes for gene: HYOU1 were set to Immunodeficiency 59 and hypoglycemia, MIM#\t233600\nReview for gene: HYOU1 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:09:37.799548+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HYOU1 as ready","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:09:37.786239+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hyou1 has been classified as Red List (Low Evidence).","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:09:32.225597+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HYOU1 was added\ngene: HYOU1 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: HYOU1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HYOU1 were set to 27913302\nPhenotypes for gene: HYOU1 were set to Immunodeficiency 59 and hypoglycemia, MIM#\t233600\nReview for gene: HYOU1 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"HYOU1","entity_type":"gene"},{"created":"2020-04-05T15:05:59.832519+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EFL1 as ready","entity_name":"EFL1","entity_type":"gene"},{"created":"2020-04-05T15:05:59.818770+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: efl1 has been classified as Green List (High Evidence).","entity_name":"EFL1","entity_type":"gene"},{"created":"2020-04-05T15:02:43.899771+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EFL1 as Green List (high evidence)","entity_name":"EFL1","entity_type":"gene"},{"created":"2020-04-05T15:02:43.891178+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: efl1 has been classified as Green List (High Evidence).","entity_name":"EFL1","entity_type":"gene"},{"created":"2020-04-05T15:02:15.872086+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EFL1 was added\ngene: EFL1 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: EFL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EFL1 were set to 28331068; 31151987\nPhenotypes for gene: EFL1 were set to Shwachman-Diamond syndrome 2, MIM#\t617941\nReview for gene: EFL1 was set to GREEN\nAdded comment: Six unrelated families reported, two had the same homozygous variant, one family single variant plus 'expression defect' identified. \nSources: Expert list","entity_name":"EFL1","entity_type":"gene"},{"created":"2020-04-05T14:57:20.437998+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC21 as ready","entity_name":"DNAJC21","entity_type":"gene"},{"created":"2020-04-05T14:57:20.428348+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc21 has been classified as Green List (High Evidence).","entity_name":"DNAJC21","entity_type":"gene"},{"created":"2020-04-05T14:57:04.179442+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJC21 as Green List (high evidence)","entity_name":"DNAJC21","entity_type":"gene"},{"created":"2020-04-05T14:57:04.170093+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc21 has been classified as Green List (High Evidence).","entity_name":"DNAJC21","entity_type":"gene"},{"created":"2020-04-05T14:56:33.365116+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJC21 was added\ngene: DNAJC21 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: DNAJC21 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DNAJC21 were set to 29700810; 28062395; 27346687\nPhenotypes for gene: DNAJC21 were set to Bone marrow failure syndrome 3, MIM#\t617052; Short stature; Exocrine pancreatic insufficiency; Pancytopaenia; Shwachman-Diamond syndrome\nReview for gene: DNAJC21 was set to GREEN\nAdded comment: Over ten unrelated families reported. \nSources: Expert list","entity_name":"DNAJC21","entity_type":"gene"},{"created":"2020-04-05T14:51:34.669102+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1953","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCD2 as ready","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:51:34.655914+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1953","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Green List (High Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:51:25.614341+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1953","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMARCD2 as Green List (high evidence)","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:51:25.598758+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1953","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Green List (High Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:51:08.142292+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1952","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMARCD2 was added\ngene: SMARCD2 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: SMARCD2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SMARCD2 were set to 28369036; 28369034\nPhenotypes for gene: SMARCD2 were set to Specific granule deficiency 2, MIM#\t617475; Neutropaenia; Neurodevelopmental abnormalities in some; Myelodysplasia\nReview for gene: SMARCD2 was set to GREEN\nAdded comment: Three unrelated families and functional data. \nSources: Expert list","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:49:22.891460+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCD2 as ready","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:49:22.877527+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Green List (High Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:49:20.043184+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMARCD2 as Green List (high evidence)","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:49:20.034301+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Green List (High Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:48:52.285800+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMARCD2 was added\ngene: SMARCD2 was added to Phagocyte Defects. Sources: Expert list\nMode of inheritance for gene: SMARCD2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SMARCD2 were set to 28369036; 28369034\nPhenotypes for gene: SMARCD2 were set to Specific granule deficiency 2, MIM#\t617475; Neutropaenia; Neurodevelopmental abnormalities in some; Myelodysplasia\nReview for gene: SMARCD2 was set to GREEN\nAdded comment: Three unrelated families and functional data. \nSources: Expert list","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-04-05T14:47:27.996622+10:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.13","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AFG3L2 was added\ngene: AFG3L2 was added to Dystonia - complex. Sources: Expert list\nMode of inheritance for gene: AFG3L2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AFG3L2 were set to 22964162; 16541453\nPhenotypes for gene: AFG3L2 were set to Spastic ataxia 5, autosomal recessive MIM#614487\nReview for gene: AFG3L2 was set to RED\nAdded comment: Dystonia is not a prominent feature of this condition. There is a single family reported with complex dystonia. Dystonia was previously observed in a family whose affected members carried an 18p chromosomal deletion that included AFG3L2. \nSources: Expert list","entity_name":"AFG3L2","entity_type":"gene"},{"created":"2020-04-05T14:41:02.678029+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Melbourne Genomics; Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-04-05T14:39:29.988749+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAGT1 as ready","entity_name":"MAGT1","entity_type":"gene"},{"created":"2020-04-05T14:39:29.978897+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: magt1 has been classified as Green List (High Evidence).","entity_name":"MAGT1","entity_type":"gene"},{"created":"2020-04-05T14:39:23.384106+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAGT1 as Green List (high evidence)","entity_name":"MAGT1","entity_type":"gene"},{"created":"2020-04-05T14:39:23.375634+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: magt1 has been classified as Green List (High Evidence).","entity_name":"MAGT1","entity_type":"gene"},{"created":"2020-04-05T14:38:47.818686+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MAGT1 was added\ngene: MAGT1 was added to Disorders of immune dysregulation. Sources: Expert list\nMode of inheritance for gene: MAGT1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: MAGT1 were set to 31036665; 25504528; 21796205; 24550228; 25956530\nPhenotypes for gene: MAGT1 were set to Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, MIM#\t300853\nReview for gene: MAGT1 was set to GREEN\nAdded comment: Multiple unrelated individuals reported, some overlap with the CDG associated with his gene. \nSources: Expert list","entity_name":"MAGT1","entity_type":"gene"},{"created":"2020-04-05T14:35:02.446684+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ITK as ready","entity_name":"ITK","entity_type":"gene"},{"created":"2020-04-05T14:35:02.437290+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: itk has been classified as Green List (High Evidence).","entity_name":"ITK","entity_type":"gene"},{"created":"2020-04-05T14:34:53.407344+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ITK as Green List (high evidence)","entity_name":"ITK","entity_type":"gene"},{"created":"2020-04-05T14:34:53.394370+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: itk has been classified as Green List (High Evidence).","entity_name":"ITK","entity_type":"gene"},{"created":"2020-04-05T14:34:24.511935+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ITK was added\ngene: ITK was added to Disorders of immune dysregulation. Sources: Expert list\nMode of inheritance for gene: ITK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ITK were set to 19425169; 22289921; 21109689\nPhenotypes for gene: ITK were set to Lymphoproliferative syndrome 1, MIM#\t613011; EBV associated B call lymphoproliferation, lymphoma\nReview for gene: ITK was set to GREEN\nAdded comment: At least three unrelated families reported. \nSources: Expert list","entity_name":"ITK","entity_type":"gene"},{"created":"2020-04-05T14:30:35.321811+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1951","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFRSF9 as ready","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:30:35.308875+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1951","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf9 has been classified as Green List (High Evidence).","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:30:13.658575+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1951","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TNFRSF9 as Green List (high evidence)","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:30:13.645305+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1951","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf9 has been classified as Green List (High Evidence).","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:29:54.673382+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1950","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNFRSF9 was added\ngene: TNFRSF9 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: TNFRSF9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TNFRSF9 were set to 30872117; 31501153\nPhenotypes for gene: TNFRSF9 were set to EBV lymphoproliferation; B-cell lymphoma; Chronic active EBV infection\nReview for gene: TNFRSF9 was set to GREEN\nAdded comment: Six unrelated individuals, two with same homozygous G109S missense variant, functional data. \nSources: Expert list","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:29:45.168211+10:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.12","user_name":"Bryony Thompson","item_type":"panel","text":"Panel name changed from Dystonia - complex_RMH to Dystonia - complex\nPanel types changed to Royal Melbourne Hospital; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-04-05T14:28:08.508305+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFRSF9 as ready","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:28:08.499327+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf9 has been classified as Green List (High Evidence).","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:28:04.535210+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TNFRSF9 as Green List (high evidence)","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:28:04.522057+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfrsf9 has been classified as Green List (High Evidence).","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:27:34.050432+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Two unrelated individuals with same homozygous G109S missense variant, some functional data. \nSources: Expert list; to: Six unrelated individuals, two with same homozygous G109S missense variant, functional data. \r\nSources: Expert list","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:27:06.582978+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TNFRSF9: Changed rating: GREEN; Changed publications: 30872117, 31501153","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:26:07.924635+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNFRSF9 was added\ngene: TNFRSF9 was added to Disorders of immune dysregulation. Sources: Expert list\nMode of inheritance for gene: TNFRSF9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TNFRSF9 were set to 30872117\nPhenotypes for gene: TNFRSF9 were set to EBV lymphoproliferation; B-cell lymphoma; Chronic active EBV infection\nReview for gene: TNFRSF9 was set to RED\nAdded comment: Two unrelated individuals with same homozygous G109S missense variant, some functional data. \nSources: Expert list","entity_name":"TNFRSF9","entity_type":"gene"},{"created":"2020-04-05T14:22:16.789423+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1949","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTPS1 as ready","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:22:16.780187+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1949","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctps1 has been classified as Green List (High Evidence).","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:22:07.959599+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1949","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTPS1 were changed from  to Immunodeficiency 24, MIM# 615897; Recurrent/chronic bacterial and viral infections (EBV, VZV); EBV lymphoproliferation; B-cell non-Hodgkin lymphoma","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:21:53.620246+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1948","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTPS1 were set to ","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:21:34.666604+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1947","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTPS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:21:13.455082+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1946","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTPS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24870241; Phenotypes: Immunodeficiency 24, MIM# 615897, Recurrent/chronic bacterial and viral infections (EBV, VZV), EBV lymphoproliferation, B-cell non-Hodgkin lymphoma; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:21:03.608302+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTPS1 as ready","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:21:03.595047+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctps1 has been classified as Green List (High Evidence).","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:20:24.900857+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTPS1 as ready","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:20:24.891780+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctps1 has been classified as Green List (High Evidence).","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:20:19.630457+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTPS1 were changed from  to Immunodeficiency 24, MIM# 615897; Recurrent/chronic bacterial and viral infections (EBV, VZV); EBV lymphoproliferation; B-cell non-Hodgkin lymphoma","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:19:56.230017+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTPS1 were set to ","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:19:30.516194+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTPS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:18:59.939668+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTPS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24870241; Phenotypes: Immunodeficiency 24, MIM# 615897, Recurrent/chronic bacterial and viral infections (EBV, VZV), EBV lymphoproliferation, B-cell non-Hodgkin lymphoma; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:18:37.014236+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTPS1 as Green List (high evidence)","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:18:37.000318+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctps1 has been classified as Green List (High Evidence).","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:18:05.117635+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CTPS1 was added\ngene: CTPS1 was added to Disorders of immune dysregulation. Sources: Expert list\nMode of inheritance for gene: CTPS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CTPS1 were set to 24870241\nPhenotypes for gene: CTPS1 were set to Immunodeficiency 24, MIM#\t615897; Recurrent/chronic bacterial and viral infections (EBV, VZV); EBV lymphoproliferation; B-cell non-Hodgkin lymphoma\nReview for gene: CTPS1 was set to GREEN\nAdded comment: At least 5 families reported. \nSources: Expert list","entity_name":"CTPS1","entity_type":"gene"},{"created":"2020-04-05T14:11:43.687792+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD27 as ready","entity_name":"CD27","entity_type":"gene"},{"created":"2020-04-05T14:11:43.674206+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd27 has been classified as Green List (High Evidence).","entity_name":"CD27","entity_type":"gene"},{"created":"2020-04-05T14:11:39.690561+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD27 as Green List (high evidence)","entity_name":"CD27","entity_type":"gene"},{"created":"2020-04-05T14:11:39.681141+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd27 has been classified as Green List (High Evidence).","entity_name":"CD27","entity_type":"gene"},{"created":"2020-04-05T14:11:06.120827+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CD27 was added\ngene: CD27 was added to Disorders of immune dysregulation. Sources: Expert list\nMode of inheritance for gene: CD27 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD27 were set to 22801960; 22197273\nPhenotypes for gene: CD27 were set to Lymphoproliferative syndrome 2, MIM#\t615122\nReview for gene: CD27 was set to GREEN\nAdded comment: At least four families reported. \nSources: Expert list","entity_name":"CD27","entity_type":"gene"},{"created":"2020-04-05T14:03:43.756070+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFB1 as ready","entity_name":"TGFB1","entity_type":"gene"},{"created":"2020-04-05T14:03:43.742251+10:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfb1 has been classified as Amber List (Moderate Evidence).","entity_name":"TGFB1","entity_type":"gene"}]}