{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2008","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2006","results":[{"created":"2020-01-03T20:14:52.215043+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846; 30423442","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:14:22.579362+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Second family identified","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:14:22.547601+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:13:56.407152+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:13:56.347761+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:13:10.712010+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:13:10.706348+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Second family identified PMID 30423442","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:13:10.676165+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:12:07.816846+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":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:11:37.553715+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:11:37.542419+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:11:19.114090+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846; 30423442","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:11:03.680092+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1475","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:11:03.663661+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1475","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:10:52.364113+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:10:52.345867+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:10:24.330366+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:10:24.266607+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:09:32.690094+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:09:27.618311+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.588","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:09:27.611451+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.588","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Second family identified in the literature.","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:09:27.578802+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.588","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:09:21.460880+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.588","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from  to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:08:57.511939+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:08:57.467156+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:08:31.379089+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846; 30423442","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:08:16.600273+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:08:16.587923+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:54.724832+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:48.442025+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:48.435959+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two families; link with regression not established.","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:48.378625+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:17.497552+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.587","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:00.838332+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.586","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Amber List (moderate evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:07:00.822247+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.586","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Amber List (Moderate Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:06:20.068028+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1474","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PDE6D: Changed rating: AMBER","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:06:06.840930+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from Joubert syndrome 22, OMIM #615665 to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:05:29.808268+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:05:29.795395+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:05:28.416005+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from Joubert syndrome 22, OMIM #615665 to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:05:19.662896+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:04:53.408058+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from  to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:04:39.633766+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.585","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:04:27.839891+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to ","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:04:13.998503+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to ","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:03:45.242198+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:03:19.652414+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Red List (low evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:03:19.591612+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:02:20.867957+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:02:20.851265+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:02:20.448234+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.584","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to ","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:02:13.064169+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to 24166846","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:02:13.063390+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from  to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:01:26.769244+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to ","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:01:21.866495+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:00:25.865029+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.583","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:00:08.689367+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Red List (low evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T20:00:08.675659+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:59:53.625049+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from  to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:59:47.551738+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.581","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:58:58.082238+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:58:38.997727+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Red List (low evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:58:38.967730+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:58:25.602652+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Red List (low evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:58:25.589337+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:57:50.508358+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:56:59.536070+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:56:48.874163+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE6D as ready","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:56:48.862406+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:56:23.800495+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDE6D were changed from  to Joubert syndrome 22, OMIM #615665","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:55:51.699928+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE6D were set to ","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:54:08.393982+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:53:38.967554+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDE6D as Red List (low evidence)","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:53:38.955368+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde6d has been classified as Red List (Low Evidence).","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:53:06.162299+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDE6D","entity_type":"gene"},{"created":"2020-01-03T19:49:56.964064+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.581","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC41A1 as ready","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:56.951908+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.581","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc41a1 has been classified as Red List (Low Evidence).","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:48.211544+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.581","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC41A1 were changed from  to Nephronophthisis","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:38.261445+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.580","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC41A1 were set to ","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:29.771444+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.579","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC41A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:07.436047+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.578","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC41A1 as Red List (low evidence)","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:49:07.424905+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.578","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc41a1 has been classified as Red List (Low Evidence).","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:48:45.296036+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC41A1: Rating: RED; Mode of pathogenicity: None; Publications: 23661805; Phenotypes: Nephronophthisis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC41A1","entity_type":"gene"},{"created":"2020-01-03T19:45:39.213087+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1474","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIM32 as ready","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:39.202364+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1474","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trim32 has been classified as Red List (Low Evidence).","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:34.565582+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1474","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIM32 were changed from  to Bardet-Biedl syndrome 11, MIM# 615988","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:23.977990+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1473","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIM32 were set to ","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:14.092541+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1472","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:06.595035+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1471","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM32 as Red List (low evidence)","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:45:06.582888+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trim32 has been classified as Red List (Low Evidence).","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:44:53.030876+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1470","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: None; Publications: 16606853; Phenotypes: Bardet-Biedl syndrome 11, MIM# 615988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:43:34.203041+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIM32 were changed from Bardet-Biedl syndrome 11, MIM# 615988 to Bardet-Biedl syndrome 11, MIM# 615988","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:43:23.154058+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIM32 as ready","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:43:23.141433+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trim32 has been classified as Red List (Low Evidence).","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:43:08.299582+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIM32 were set to 16606853","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:42:42.330453+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIM32 were changed from  to Bardet-Biedl syndrome 11, MIM# 615988","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:42:16.331642+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIM32 were set to ","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:41:50.522436+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIM32 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:41:24.475911+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIM32 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:40:58.515644+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIM32","entity_type":"gene"}]}