{"count":220751,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2007","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2005","results":[{"created":"2020-01-04T08:38:17.885941+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: got2 has been classified as Green List (High Evidence).","entity_name":"GOT2","entity_type":"gene"},{"created":"2020-01-04T08:37:37.907438+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GOT2 was added\ngene: GOT2 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: GOT2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GOT2 were set to 31422819\nPhenotypes for gene: GOT2 were set to Epileptic encephalopathy, early infantile, 82, MIM#\t618721\nReview for gene: GOT2 was set to GREEN\nAdded comment: Four individuals from three unrelated families reported. Treatment with pyridoxine and serine ameliorated the phenotype. \nSources: Expert list","entity_name":"GOT2","entity_type":"gene"},{"created":"2020-01-03T21:20:44.052794+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCDC2 were changed from Nephronophthisis 19, MIM# 616217 to Nephronophthisis 19, MIM# 616217","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:20:41.552150+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCDC2 as ready","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:20:41.538839+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.44","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":"2020-01-03T21:20:17.235402+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCDC2 were changed from  to Nephronophthisis 19, MIM# 616217","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:19:50.531689+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCDC2 were set to ","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:18:26.802043+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.43","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":"2020-01-03T21:17:51.507410+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCDC2 as Amber List (moderate evidence)","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:17:51.494787+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.42","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":"2020-01-03T21:17:16.674587+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.41","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: None","entity_name":"DCDC2","entity_type":"gene"},{"created":"2020-01-03T21:13:58.913863+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXC1 as ready","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-01-03T21:13:58.901901+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxc1 has been classified as Red List (Low Evidence).","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-01-03T21:13:40.997199+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXC1 as Red List (low evidence)","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-01-03T21:13:40.981469+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxc1 has been classified as Red List (Low Evidence).","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-01-03T21:13:05.448361+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FOXC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-01-03T21:07:35.081040+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.605","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLIS2 as ready","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:07:35.063606+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.605","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glis2 has been classified as Amber List (Moderate Evidence).","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:07:19.859046+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.605","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLIS2 were set to 17618285, 23559409","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:07:09.941556+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.604","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLIS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:07:00.435437+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.603","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLIS2 were set to ","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:06:43.794206+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLIS2 as ready","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:06:43.783733+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glis2 has been classified as Amber List (Moderate Evidence).","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:06:31.801358+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLIS2 were changed from  to Nephronophthisis 7, OMIM#611498","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:06:26.119876+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.602","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLIS2 were changed from  to Nephronophthisis 7, OMIM#611498","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:05:36.720564+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.601","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GLIS2 as Amber List (moderate evidence)","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:05:36.706575+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.601","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glis2 has been classified as Amber List (Moderate Evidence).","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:05:32.020473+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLIS2 were set to ","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:05:15.223604+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.600","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GLIS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 17618285, 23559409; Phenotypes: Nephronophthisis 7, OMIM#611498; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:04:55.383003+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLIS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:04:23.944514+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GLIS2 as Amber List (moderate evidence)","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:04:23.928207+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glis2 has been classified as Amber List (Moderate Evidence).","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:03:49.207817+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GLIS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 17618285, 23559409; Phenotypes: Nephronophthisis 7, OMIM#611498; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLIS2","entity_type":"gene"},{"created":"2020-01-03T21:00:34.229105+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.600","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT57 as ready","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T21:00:34.217580+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.600","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift57 has been classified as Red List (Low Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T21:00:05.549234+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.600","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT57 were changed from  to Orofaciodigital syndrome XVIII, MIM# 617927","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:59:48.349227+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.599","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT57 were set to ","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:59:31.563291+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.598","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT57 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:58:46.602691+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.597","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT57 as Red List (low evidence)","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:58:46.590682+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.597","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift57 has been classified as Red List (Low Evidence).","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:58:28.290313+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.596","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT57: Rating: RED; Mode of pathogenicity: None; Publications: 27060890; Phenotypes: Orofaciodigital syndrome XVIII, MIM# 617927; Mode of inheritance: None","entity_name":"IFT57","entity_type":"gene"},{"created":"2020-01-03T20:56:09.393326+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.596","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT74 as ready","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:56:09.382400+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift74 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:58.528241+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT74 as ready","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:58.514708+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift74 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:56.665986+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.596","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT74 as Amber List (moderate evidence)","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:56.652773+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift74 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:37.433541+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.595","user_name":"Zornitza Stark","item_type":"entity","text":"gene: IFT74 was added\ngene: IFT74 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: IFT74 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IFT74 were set to 27486776\nPhenotypes for gene: IFT74 were set to Bardet-Biedl syndrome 20, MIM# 617119\nReview for gene: IFT74 was set to AMBER\nAdded comment: Single family and functional data. \nSources: Expert list","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:26.592076+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT74 as Amber List (moderate evidence)","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:55:26.581216+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift74 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:54:22.748337+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT74 as Amber List (moderate evidence)","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:54:22.735246+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift74 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:53:21.475092+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"gene: IFT74 was added\ngene: IFT74 was added to Bardet Biedl syndrome_VCGS. Sources: Expert list\nMode of inheritance for gene: IFT74 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IFT74 were set to 27486776\nPhenotypes for gene: IFT74 were set to Bardet-Biedl syndrome 20, MIM# 617119\nReview for gene: IFT74 was set to AMBER\nAdded comment: Single family plus functional data. \nSources: Expert list","entity_name":"IFT74","entity_type":"gene"},{"created":"2020-01-03T20:49:21.218416+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT81 as ready","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:49:21.213197+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Three families with skeletal dysplasia, one with nephronophthisis, one with eye phenotype.","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:49:21.182866+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:49:11.106934+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Amber List (moderate evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:49:11.095944+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:48:42.134446+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Amber List (moderate evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:48:42.121475+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:47:48.138929+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:47:22.895350+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:46:57.427391+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:46:49.508182+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT81 were changed from  to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:45:49.268153+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:45:49.257077+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:45:11.564279+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.593","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:44:36.496264+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822; 30080953","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:44:17.418673+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:44:17.398305+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:43:55.831018+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:43:29.403127+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:43:28.997318+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:43:00.387558+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:42:21.600522+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:42:21.587047+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:41:33.493601+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT81 as ready","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:41:33.487624+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Single family with renal phenotype.","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:41:33.440708+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Red List (Low Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:41:23.532240+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:41:09.194565+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.592","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:39:08.995770+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to ","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:39:03.249253+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT81 were changed from  to Short-rib thoracic dysplasia 19 with or without polydactyly; OMIM #617895","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:37:47.328666+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.591","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:37:47.314669+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.591","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:37:41.389806+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822; 26275418","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:36:55.742153+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Third report identified.","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:36:55.712618+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to 27666822","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:36:30.135361+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Green List (high evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:36:30.015872+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Green List (High Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:34:25.370224+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Amber List (moderate evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:34:25.353639+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:34:08.058303+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.590","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT81 were set to ","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:33:53.659356+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.589","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IFT81 as Amber List (moderate evidence)","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:33:53.644524+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.589","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:33:33.891597+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.588","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:33:24.121300+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:31:49.417353+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT81 as ready","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:31:49.404248+11:00","panel_name":"Skeletal dysplasia Fetal_MelbourneGenomics_VCGS","panel_id":28,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift81 has been classified as Amber List (Moderate Evidence).","entity_name":"IFT81","entity_type":"gene"},{"created":"2020-01-03T20:31:36.214797+11:00","panel_name":"Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS","panel_id":179,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT81 as ready","entity_name":"IFT81","entity_type":"gene"}]}