{"count":220423,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1507","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1505","results":[{"created":"2020-11-10T20:47:17.059734+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OCLN as ready","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:47:17.039530+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ocln has been classified as Green List (High Evidence).","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:47:13.349339+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5344","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OCLN: Rating: GREEN; Mode of pathogenicity: None; Publications: 20727516, 32240828, 29192239, 28386946; Phenotypes: Pseudo-TORCH syndrome 1, MIM#251290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:44:38.392511+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OCLN were changed from  to Pseudo-TORCH syndrome 1, MIM#251290","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:43:56.027885+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OCLN were set to ","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:43:22.766668+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OCLN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:42:50.357606+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OCLN: Rating: GREEN; Mode of pathogenicity: None; Publications: 20727516, 32240828, 29192239, 28386946; Phenotypes: Pseudo-TORCH syndrome 1, MIM#251290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OCLN","entity_type":"gene"},{"created":"2020-11-10T20:38:12.457411+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC6 as ready","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-11-10T20:38:12.446122+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc6 has been classified as Green List (High Evidence).","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-11-10T20:38:09.230647+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC6 were changed from  to Cockayne syndrome, type B, MIM#133540","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-11-10T20:37:35.487570+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-11-10T20:37:00.454956+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ERCC6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cockayne syndrome, type B, MIM#133540; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-11-10T20:33:02.378802+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JAM3 as ready","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:33:02.366882+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jam3 has been classified as Green List (High Evidence).","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:32:51.942391+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: JAM3 were changed from  to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:32:17.251706+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3186","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: JAM3 were set to ","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:31:45.908438+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3185","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:31:11.537274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:30:24.910867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5344","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JAM3 as ready","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:30:24.902703+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5344","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jam3 has been classified as Green List (High Evidence).","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:30:17.114993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5344","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: JAM3 were changed from  to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:29:58.032002+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5343","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: JAM3 were set to ","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:29:34.576674+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5342","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:29:16.174396+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5341","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:28:31.481109+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.243","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JAM3 as ready","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:28:31.470593+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.243","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jam3 has been classified as Green List (High Evidence).","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:28:28.809950+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.243","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: JAM3 were changed from  to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:28:01.599576+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.242","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: JAM3 were set to ","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:27:24.112201+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.241","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:26:49.500403+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:25:50.162538+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JAM3 as ready","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:25:50.151145+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jam3 has been classified as Green List (High Evidence).","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:25:47.267766+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: JAM3 were changed from  to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:25:15.649953+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: JAM3 were set to ","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:24:43.185163+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:24:09.773511+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"JAM3","entity_type":"gene"},{"created":"2020-11-10T20:21:11.901782+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFIH1 as ready","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:21:11.889374+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ifih1 has been classified as Green List (High Evidence).","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:21:08.075746+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFIH1 were changed from  to Aicardi-Goutieres syndrome 7, MIM#615846","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:20:35.560582+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFIH1 were set to ","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:20:06.422725+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFIH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:19:30.178069+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFIH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24686847; Phenotypes: Aicardi-Goutieres syndrome 7, MIM#615846; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IFIH1","entity_type":"gene"},{"created":"2020-11-10T20:17:18.655298+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADAR as ready","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:17:18.647135+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adar has been classified as Green List (High Evidence).","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:17:14.874266+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADAR were changed from  to Aicardi-Goutieres syndrome 6, MIM#615010","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:16:42.759748+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADAR were set to ","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:16:10.687696+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ADAR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:15:37.585094+11:00","panel_name":"Brain Calcification","panel_id":58,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ADAR: Rating: GREEN; Mode of pathogenicity: None; Publications: 23001123, 24262145; Phenotypes: Aicardi-Goutieres syndrome 6, MIM#615010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-11-10T20:07:56.698442+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2020-11-10T17:15:47.977918+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: POLE: Changed rating: GREEN","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:15:32.823019+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLE as ready","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:15:32.817742+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: The association with microcephaly relates to IMAGE-I syndrome.","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:15:32.780994+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pole has been classified as Green List (High Evidence).","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:15:03.227532+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLE were changed from FILS syndrome 615139; IMAGE-I syndrome 618336 to IMAGE-I syndrome, MIM# 618336","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:13:42.123058+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.497","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POLE as Green List (high evidence)","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T17:13:42.114044+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.497","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pole has been classified as Green List (High Evidence).","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-10T12:21:15.217384+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.496","user_name":"Elena Savva","item_type":"entity","text":"gene: POLE was added\ngene: POLE was added to Microcephaly. Sources: Literature\nMode of inheritance for gene: POLE was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POLE were set to PMID: 30503519\nPhenotypes for gene: POLE were set to FILS syndrome 615139; IMAGE-I syndrome 618336\nReview for gene: POLE was set to GREEN\nAdded comment: PMID: 30503519 - microcephaly reported in multiple patients with biallelic LOF variants \nSources: Literature","entity_name":"POLE","entity_type":"gene"},{"created":"2020-11-09T18:18:53.717867+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCKAP1 as ready","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:18:53.705769+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nckap1 has been classified as Green List (High Evidence).","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:18:50.848899+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCKAP1 were changed from  to Intellectual disability; autism","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:18:21.399475+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCKAP1 were set to ","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:17:09.207588+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:16:37.654405+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:15:55.569553+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5341","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCKAP1 as ready","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:15:55.558755+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5341","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nckap1 has been classified as Green List (High Evidence).","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:15:48.064053+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5341","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCKAP1 were changed from  to Intellectual disability; autism","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:15:24.951278+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5340","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCKAP1 were set to ","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:14:58.358643+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5339","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:14:35.916051+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5338","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:13:47.565550+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCKAP1 as ready","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:13:47.545257+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nckap1 has been classified as Green List (High Evidence).","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:13:41.866269+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCKAP1 were changed from  to Intellectual disability; autism","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:12:51.547101+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCKAP1 were set to ","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:11:15.888788+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3182","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T18:10:22.729354+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NCKAP1","entity_type":"gene"},{"created":"2020-11-09T17:14:44.280048+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to New South Wales Health Pathology","entity_name":null,"entity_type":null},{"created":"2020-11-09T16:42:05.130205+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZBTB16 was added\ngene: ZBTB16 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ZBTB16 was set to Unknown","entity_name":"ZBTB16","entity_type":"gene"},{"created":"2020-11-09T16:42:05.077410+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VHL was added\ngene: VHL was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: VHL was set to Unknown","entity_name":"VHL","entity_type":"gene"},{"created":"2020-11-09T16:42:05.012582+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIM33 was added\ngene: TRIM33 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM33 was set to Unknown","entity_name":"TRIM33","entity_type":"gene"},{"created":"2020-11-09T16:42:04.945609+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIM27 was added\ngene: TRIM27 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM27 was set to Unknown","entity_name":"TRIM27","entity_type":"gene"},{"created":"2020-11-09T16:42:04.863950+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIM24 was added\ngene: TRIM24 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM24 was set to Unknown","entity_name":"TRIM24","entity_type":"gene"},{"created":"2020-11-09T16:42:04.780045+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TPR was added\ngene: TPR was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TPR was set to Unknown","entity_name":"TPR","entity_type":"gene"},{"created":"2020-11-09T16:42:04.728023+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TP53 was added\ngene: TP53 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TP53 was set to Unknown","entity_name":"TP53","entity_type":"gene"},{"created":"2020-11-09T16:42:04.675274+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR2 was added\ngene: TGFBR2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TGFBR2 was set to Unknown","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-11-09T16:42:04.623127+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TFG was added\ngene: TFG was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TFG was set to Unknown","entity_name":"TFG","entity_type":"gene"},{"created":"2020-11-09T16:42:04.570365+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TET2 was added\ngene: TET2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TET2 was set to Unknown","entity_name":"TET2","entity_type":"gene"},{"created":"2020-11-09T16:42:04.517968+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCF12 was added\ngene: TCF12 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TCF12 was set to Unknown","entity_name":"TCF12","entity_type":"gene"},{"created":"2020-11-09T16:42:04.464123+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBL1XR1 was added\ngene: TBL1XR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TBL1XR1 was set to Unknown","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2020-11-09T16:42:04.411027+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TAF15 was added\ngene: TAF15 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TAF15 was set to Unknown","entity_name":"TAF15","entity_type":"gene"},{"created":"2020-11-09T16:42:04.360055+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TACC3 was added\ngene: TACC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TACC3 was set to Unknown","entity_name":"TACC3","entity_type":"gene"},{"created":"2020-11-09T16:42:04.307708+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TACC1 was added\ngene: TACC1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TACC1 was set to Unknown","entity_name":"TACC1","entity_type":"gene"},{"created":"2020-11-09T16:42:04.256264+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SUFU was added\ngene: SUFU was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SUFU was set to Unknown","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-11-09T16:42:04.204487+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STAT5B was added\ngene: STAT5B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: STAT5B was set to Unknown","entity_name":"STAT5B","entity_type":"gene"},{"created":"2020-11-09T16:42:04.153641+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SRD5A2 was added\ngene: SRD5A2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SRD5A2 was set to Unknown","entity_name":"SRD5A2","entity_type":"gene"},{"created":"2020-11-09T16:42:04.102152+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMAD4 was added\ngene: SMAD4 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SMAD4 was set to Unknown","entity_name":"SMAD4","entity_type":"gene"},{"created":"2020-11-09T16:42:04.042418+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SDHD was added\ngene: SDHD was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHD was set to Unknown","entity_name":"SDHD","entity_type":"gene"},{"created":"2020-11-09T16:42:03.989969+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SDHC was added\ngene: SDHC was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHC was set to Unknown","entity_name":"SDHC","entity_type":"gene"},{"created":"2020-11-09T16:42:03.933305+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SDHB was added\ngene: SDHB was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHB was set to Unknown","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-11-09T16:42:03.875822+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SDHAF2 was added\ngene: SDHAF2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHAF2 was set to Unknown","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-11-09T16:42:03.805848+11:00","panel_name":"Incidentalome_NSW","panel_id":3437,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SDHA was added\ngene: SDHA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHA was set to Unknown","entity_name":"SDHA","entity_type":"gene"}]}