{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2011","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2009","results":[{"created":"2020-01-03T14:53:08.774471+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCDC2 were set to ","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T14:50:41.166690+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DCDC2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T14:50:32.423033+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCDC2 as Amber List (moderate evidence)","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T14:50:32.411490+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcdc2 has been classified as Amber List (Moderate Evidence).","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T14:50:20.219001+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DCDC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25557784; Phenotypes: Nephronophthisis 19, MIM# 616217; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T14:49:24.953937+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.34","user_name":"chirag patel","item_type":"entity","text":"Classified gene: CEP120 as Amber List (moderate evidence)","entity_name":"CEP120","entity_type":"gene"},{"created":"2020-01-03T14:49:24.942740+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.34","user_name":"chirag patel","item_type":"entity","text":"Gene: cep120 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP120","entity_type":"gene"},{"created":"2020-01-03T14:49:11.247151+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.33","user_name":"chirag patel","item_type":"entity","text":"reviewed gene: CEP120: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 25361962; Phenotypes: Joubert syndrome 31, OMIM #617761, Short-rib thoracic dysplasia 13 with or without polydactyly, OMIM #616300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP120","entity_type":"gene"},{"created":"2020-01-03T14:42:10.765898+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.33","user_name":"chirag patel","item_type":"entity","text":"Classified gene: C2CD3 as Red List (low evidence)","entity_name":"C2CD3","entity_type":"gene"},{"created":"2020-01-03T14:42:10.754507+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.33","user_name":"chirag patel","item_type":"entity","text":"Gene: c2cd3 has been classified as Red List (Low Evidence).","entity_name":"C2CD3","entity_type":"gene"},{"created":"2020-01-03T14:42:00.174696+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.32","user_name":"chirag patel","item_type":"entity","text":"changed review comment from: Renal phenotype not commonly seen in this group.; to: Renal phenotype not commonly seen in this ciliopathy, so not a renal ciliopathy","entity_name":"C2CD3","entity_type":"gene"},{"created":"2020-01-03T14:41:33.501058+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.32","user_name":"chirag patel","item_type":"entity","text":"reviewed gene: C2CD3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"C2CD3","entity_type":"gene"},{"created":"2020-01-03T14:36:07.849981+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.32","user_name":"chirag patel","item_type":"entity","text":"Classified gene: B9D1 as Red List (low evidence)","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-01-03T14:36:07.837128+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.32","user_name":"chirag patel","item_type":"entity","text":"Gene: b9d1 has been classified as Red List (Low Evidence).","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-01-03T14:35:58.974046+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.31","user_name":"chirag patel","item_type":"entity","text":"reviewed gene: B9D1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ?Meckel syndrome 9, OMIM #614209, Joubert syndrome 27, OMIM #617120; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-01-03T13:59:49.476136+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD151 as ready","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:59:49.459190+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Red List (Low Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:59:39.946711+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD151 were changed from  to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:57:45.948065+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD151 were set to 15265795; 29138120","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:57:20.722798+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CD151 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:56:53.467474+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.11","user_name":"chirag patel","item_type":"entity","text":"Classified gene: OCRL as Red List (low evidence)","entity_name":"OCRL","entity_type":"gene"},{"created":"2020-01-03T13:56:53.443423+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.11","user_name":"chirag patel","item_type":"entity","text":"Gene: ocrl has been classified as Red List (Low Evidence).","entity_name":"OCRL","entity_type":"gene"},{"created":"2020-01-03T13:56:26.707492+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.10","user_name":"chirag patel","item_type":"entity","text":"Classified gene: OCRL as Red List (low evidence)","entity_name":"OCRL","entity_type":"gene"},{"created":"2020-01-03T13:56:26.675610+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.10","user_name":"chirag patel","item_type":"entity","text":"Gene: ocrl has been classified as Red List (Low Evidence).","entity_name":"OCRL","entity_type":"gene"},{"created":"2020-01-03T13:56:01.098575+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD151 as Red List (low evidence)","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:56:01.031574+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Red List (Low Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:55:36.843539+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD151 were set to ","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:55:09.175585+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CD151 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:54:42.652638+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD151 as Red List (low evidence)","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:54:41.995782+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Red List (Low Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2020-01-03T13:54:39.142269+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.8","user_name":"chirag patel","item_type":"entity","text":"reviewed gene: OCRL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"OCRL","entity_type":"gene"},{"created":"2020-01-03T13:48:42.228097+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGQ as ready","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:48:42.134225+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigq has been classified as Green List (High Evidence).","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:47:51.300007+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIGQ as Green List (high evidence)","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:47:51.123071+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigq has been classified as Green List (High Evidence).","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:47:25.418710+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIGQ was added\ngene: PIGQ was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: PIGQ was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGQ were set to 25558065; 24463883; 31148362\nPhenotypes for gene: PIGQ were set to Epileptic encephalopathy, early infantile, 77, MIM#\t618548\nReview for gene: PIGQ was set to GREEN\nAdded comment: Three unrelated families reported. \nSources: Expert list","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:39:45.879680+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGQ as ready","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:39:45.861745+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigq has been classified as Green List (High Evidence).","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:39:41.444893+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIGQ as Green List (high evidence)","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:39:41.426008+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigq has been classified as Green List (High Evidence).","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T13:39:08.468320+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIGQ was added\ngene: PIGQ was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: PIGQ was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGQ were set to 25558065; 24463883; 31148362\nPhenotypes for gene: PIGQ were set to Epileptic encephalopathy, early infantile, 77, MIM#\t618548\nReview for gene: PIGQ was set to GREEN\nAdded comment: Three unrelated families reported. \nSources: Expert list","entity_name":"PIGQ","entity_type":"gene"},{"created":"2020-01-03T12:49:21.130005+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTRK2 as ready","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:49:21.119110+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk2 has been classified as Green List (High Evidence).","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:49:15.439061+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NTRK2 as Green List (high evidence)","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:49:15.427872+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk2 has been classified as Green List (High Evidence).","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:49:02.374762+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1465","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NTRK2 was added\ngene: NTRK2 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Expert list\nMode of inheritance for gene: NTRK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NTRK2 were set to 15494731; 27884935; 29100083\nPhenotypes for gene: NTRK2 were set to Obesity, hyperphagia, and developmental delay, MIM# 613886\nReview for gene: NTRK2 was set to GREEN\nAdded comment: Three unrelated individuals reported with this phenotype.\r\nNote recurrent missense in this gene also causes EE. \nSources: Expert list","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:47:10.987661+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTRK2 as ready","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:47:10.976203+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk2 has been classified as Green List (High Evidence).","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:47:00.442689+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NTRK2 were changed from  to Epileptic encephalopathy, early infantile, 58, MIM# 617830; Obesity, hyperphagia, and developmental delay, MIM# 613886","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:46:57.730873+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NTRK2 were set to ","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:46:30.956057+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.566","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NTRK2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:46:11.476005+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NTRK2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29100083, 15494731, 27884935, 29100083; Phenotypes: Epileptic encephalopathy, early infantile, 58, MIM# 617830, Obesity, hyperphagia, and developmental delay, MIM# 613886; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:42:34.775197+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTRK2 as ready","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:42:34.762562+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk2 has been classified as Green List (High Evidence).","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:39:27.658503+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NTRK2 as Green List (high evidence)","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:39:27.646029+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk2 has been classified as Green List (High Evidence).","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:38:49.988353+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NTRK2 was added\ngene: NTRK2 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: NTRK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NTRK2 were set to 29100083\nPhenotypes for gene: NTRK2 were set to Epileptic encephalopathy, early infantile, 58, MIM#\t617830\nReview for gene: NTRK2 was set to GREEN\nAdded comment: Four unrelated individuals with recurrent de novo missense variant in this gene reported. \nSources: Expert list","entity_name":"NTRK2","entity_type":"gene"},{"created":"2020-01-03T12:36:14.266142+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADAM22 was added\ngene: ADAM22 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: ADAM22 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADAM22 were set to 27066583; 30237576\nPhenotypes for gene: ADAM22 were set to Epileptic encephalopathy, early infantile, 61, MIM#\t617933\nReview for gene: ADAM22 was set to AMBER\nAdded comment: Two families reported; the second one as part of a large consanguineous cohort. \nSources: Expert list","entity_name":"ADAM22","entity_type":"gene"},{"created":"2020-01-03T12:35:20.201131+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADAM22 as Amber List (moderate evidence)","entity_name":"ADAM22","entity_type":"gene"},{"created":"2020-01-03T12:35:20.187252+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adam22 has been classified as Amber List (Moderate Evidence).","entity_name":"ADAM22","entity_type":"gene"},{"created":"2020-01-03T12:34:32.387932+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADAM22 was added\ngene: ADAM22 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: ADAM22 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADAM22 were set to 27066583; 30237576\nPhenotypes for gene: ADAM22 were set to Epileptic encephalopathy, early infantile, 61, MIM#\t617933\nReview for gene: ADAM22 was set to AMBER\nAdded comment: Two families reported; the second one as part of a large consanguineous cohort. \nSources: Expert list","entity_name":"ADAM22","entity_type":"gene"},{"created":"2020-01-03T12:29:55.067928+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHACTR1 as ready","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:29:55.055662+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phactr1 has been classified as Green List (High Evidence).","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:29:13.718789+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PHACTR1 as Green List (high evidence)","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:29:13.706011+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phactr1 has been classified as Green List (High Evidence).","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:28:56.177856+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PHACTR1 was added\ngene: PHACTR1 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: PHACTR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PHACTR1 were set to 30256902\nPhenotypes for gene: PHACTR1 were set to Epileptic encephalopathy, early infantile, 70, MIM#\t618298\nReview for gene: PHACTR1 was set to GREEN\nAdded comment: Three unrelated individuals reported with de novo variants in this gene. \nSources: Expert list","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:28:54.595738+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHACTR1 as ready","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:28:54.582932+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phactr1 has been classified as Green List (High Evidence).","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:28:49.440131+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PHACTR1 as Green List (high evidence)","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:28:49.428801+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phactr1 has been classified as Green List (High Evidence).","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:27:36.676173+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PHACTR1 as Green List (high evidence)","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:27:36.663483+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phactr1 has been classified as Green List (High Evidence).","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:26:53.921085+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PHACTR1 was added\ngene: PHACTR1 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: PHACTR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PHACTR1 were set to 23033978; 30256902\nPhenotypes for gene: PHACTR1 were set to Epileptic encephalopathy, early infantile, 70, MIM#\t618298\nReview for gene: PHACTR1 was set to GREEN\nAdded comment: Three unrelated individuals reported with de novo variants in this gene. \nSources: Expert list","entity_name":"PHACTR1","entity_type":"gene"},{"created":"2020-01-03T12:24:09.930926+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRB1 as ready","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:24:09.919233+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb1 has been classified as Green List (High Evidence).","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:24:01.134953+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GABRB1 as Green List (high evidence)","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:24:01.123910+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb1 has been classified as Green List (High Evidence).","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:23:43.332318+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.561","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GABRB1 was added\ngene: GABRB1 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: GABRB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GABRB1 were set to 23934111; 27273810; 31618474\nPhenotypes for gene: GABRB1 were set to Epileptic encephalopathy, early infantile, 45, MIM#\t617153\nReview for gene: GABRB1 was set to GREEN\nAdded comment: Three individuals reported, two as part of large epilepsy cohorts. \nSources: Expert list","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:22:58.910901+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRB1 as ready","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:22:58.896243+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb1 has been classified as Green List (High Evidence).","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:22:41.632753+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GABRB1 as Green List (high evidence)","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:22:41.620485+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb1 has been classified as Green List (High Evidence).","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:21:18.786220+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GABRB1 was added\ngene: GABRB1 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: GABRB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GABRB1 were set to 23934111; 27273810; 31618474\nPhenotypes for gene: GABRB1 were set to Epileptic encephalopathy, early infantile, 45, MIM#\t617153\nReview for gene: GABRB1 was set to GREEN\nAdded comment: Three individuals reported, two as part of large epilepsy cohorts. \nSources: Expert list","entity_name":"GABRB1","entity_type":"gene"},{"created":"2020-01-03T12:15:01.964463+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.560","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRA2 as ready","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:15:01.951738+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.560","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabra2 has been classified as Green List (High Evidence).","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:14:53.676675+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.560","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GABRA2 were changed from  to Epileptic encephalopathy, early infantile, 78, MIM# 618557","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:14:38.353592+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GABRA2 were set to ","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:14:24.328689+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.558","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GABRA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:14:05.929880+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.557","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GABRA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29422393; Phenotypes: Epileptic encephalopathy, early infantile, 78, MIM# 618557; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:12:56.665287+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRA2 as ready","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:12:56.653493+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabra2 has been classified as Green List (High Evidence).","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:12:50.697133+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GABRA2 as Green List (high evidence)","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:12:50.685082+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabra2 has been classified as Green List (High Evidence).","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:11:39.688196+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GABRA2 was added\ngene: GABRA2 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: GABRA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GABRA2 were set to 29961870; 31032849; 29422393\nPhenotypes for gene: GABRA2 were set to Epileptic encephalopathy, early infantile, 78, MIM#\t618557\nReview for gene: GABRA2 was set to GREEN\nAdded comment: Five unrelated individuals reported in three publications. \nSources: Expert list","entity_name":"GABRA2","entity_type":"gene"},{"created":"2020-01-03T12:08:31.102938+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.557","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUF1 as ready","entity_name":"GUF1","entity_type":"gene"},{"created":"2020-01-03T12:08:31.090420+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.557","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: guf1 has been classified as Red List (Low Evidence).","entity_name":"GUF1","entity_type":"gene"},{"created":"2020-01-03T12:08:21.179351+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.557","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GUF1 was added\ngene: GUF1 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: GUF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GUF1 were set to 26486472\nPhenotypes for gene: GUF1 were set to Epileptic encephalopathy, early infantile, 40, MIM#\t617065\nReview for gene: GUF1 was set to RED\nAdded comment: Single family reported with homozygous missense in three sibs. \nSources: Expert list","entity_name":"GUF1","entity_type":"gene"},{"created":"2020-01-03T12:06:43.168114+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUF1 as ready","entity_name":"GUF1","entity_type":"gene"},{"created":"2020-01-03T12:06:43.155776+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: guf1 has been classified as Red List (Low Evidence).","entity_name":"GUF1","entity_type":"gene"},{"created":"2020-01-03T12:06:36.163747+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GUF1 was added\ngene: GUF1 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: GUF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GUF1 were set to 26486472\nPhenotypes for gene: GUF1 were set to Epileptic encephalopathy, early infantile, 40, MIM#\t617065\nReview for gene: GUF1 was set to RED\nAdded comment: Single family reported with homozygous missense in three sibs. \nSources: Expert list","entity_name":"GUF1","entity_type":"gene"}]}