{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2009","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2007","results":[{"created":"2020-01-03T19:40:29.724382+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM32 as Red List (low evidence)","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:40:29.710741+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.1","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":"2020-01-03T19:39:48.322664+11:00","panel_name":"Bardet Biedl syndrome_VCGS","panel_id":53,"panel_version":"0.0","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":"2020-01-03T19:39:09.259559+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIM32 as ready","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:39:09.245210+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.9","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":"2020-01-03T19:39:05.784727+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.9","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":"2020-01-03T19:38:39.372143+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIM32 were set to ","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:38:02.779611+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM32 as Red List (low evidence)","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:38:02.767046+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.7","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":"2020-01-03T19:37:09.966385+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.6","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":"2020-01-03T19:36:44.782704+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM32 as Red List (low evidence)","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:36:44.713743+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.6","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":"2020-01-03T19:36:08.306207+11:00","panel_name":"Polydactyly_VCGS","panel_id":159,"panel_version":"0.5","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":"2020-01-03T19:35:22.493010+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIM32 as ready","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:35:22.480794+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.24","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":"2020-01-03T19:35:19.224068+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.24","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":"2020-01-03T19:34:53.292851+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIM32 were set to ","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:34:24.132240+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.23","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":"2020-01-03T19:33:39.385899+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM32 as Red List (low evidence)","entity_name":"TRIM32","entity_type":"gene"},{"created":"2020-01-03T19:33:39.371967+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.22","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":"2020-01-03T19:33:05.123777+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.21","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":"2020-01-03T17:03:39.983402+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPNPEP3 as ready","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:03:39.972250+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:03:33.924006+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":"Marked gene: XPNPEP3 as ready","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:03:33.908457+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":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:03:27.127063+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPNPEP3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:02:57.109932+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:02:31.804221+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:02:31.742451+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:02:03.160125+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":"Phenotypes for gene: XPNPEP3 were changed from  to Nephronophthisis-like nephropathy 1, OMIM #613159","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:54.474225+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1469","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPNPEP3 were set to ","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:45.641514+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1468","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:37.850096+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:37.836005+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:26.049195+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPNPEP3 were set to ","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:01:25.247066+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:53.980839+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPNPEP3 were changed from  to Nephronophthisis-like nephropathy 1, OMIM #613159","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:32.636947+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPNPEP3 as ready","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:32.625582+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:22.524394+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:22.508202+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T17:00:14.651963+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPNPEP3 were changed from  to Nephronophthisis-like nephropathy 1, OMIM #613159","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:59:50.858330+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:59:50.795626+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:59:20.283786+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.576","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPNPEP3 were set to ","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:59:09.151232+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:58:26.497708+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPNPEP3 as ready","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:58:26.485963+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:58:14.935807+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.575","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:58:05.361536+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:57:55.318452+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:57:55.303440+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:57:23.644943+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:57:23.633643+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:57:17.052282+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.573","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:56:35.817946+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPNPEP3 were changed from  to Nephronophthisis-like nephropathy 1, OMIM #613159","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:56:09.395203+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPNPEP3 were set to ","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:55:46.259347+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPNPEP3 as Red List (low evidence)","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:55:46.218315+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpnpep3 has been classified as Red List (Low Evidence).","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:54:49.320430+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPNPEP3","entity_type":"gene"},{"created":"2020-01-03T16:51:14.674386+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.573","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF423 as ready","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:51:14.662559+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.573","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:50:46.971895+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF423 as ready","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:50:46.957826+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:50:46.310120+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.573","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF423 were changed from  to Joubert syndrome 19, OMIM# 614844","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:50:33.098933+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF423 were changed from Joubert syndrome 19, OMIM# 614844 to Joubert syndrome 19, OMIM# 614844","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:50:08.835597+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF423 were changed from Joubert syndrome 19, OMIM# 614844 to Joubert syndrome 19, OMIM# 614844","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:49:50.748816+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.572","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF423 were set to ","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:49:39.531911+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF423 were changed from  to Joubert syndrome 19, OMIM# 614844","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:49:25.114683+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.571","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:48:51.909930+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF423 were set to ","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:48:44.933525+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.570","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Red List (low evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:48:44.920071+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.570","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:48:19.743393+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:48:11.008026+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:47:15.426898+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF423 as ready","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:47:15.413552+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:47:14.940956+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Red List (low evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:47:14.929061+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:46:59.168181+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF423 were changed from  to Joubert syndrome 19, OMIM# 614844","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:46:37.742692+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:46:25.476657+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF423 were set to ","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:45:38.625494+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:45:06.380991+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Red List (low evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:45:06.366817+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Red List (Low Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:44:31.929494+11:00","panel_name":"Ciliopathies_VCGS","panel_id":84,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-01-03T16:11:01.436905+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.20","user_name":"chirag patel","item_type":"entity","text":"Classified gene: NPHS2 as Red List (low evidence)","entity_name":"NPHS2","entity_type":"gene"},{"created":"2020-01-03T16:11:01.424792+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.20","user_name":"chirag patel","item_type":"entity","text":"Gene: nphs2 has been classified as Red List (Low Evidence).","entity_name":"NPHS2","entity_type":"gene"},{"created":"2020-01-03T16:10:34.238576+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.20","user_name":"chirag patel","item_type":"entity","text":"Classified gene: NPHS2 as Red List (low evidence)","entity_name":"NPHS2","entity_type":"gene"},{"created":"2020-01-03T16:10:34.170583+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.20","user_name":"chirag patel","item_type":"entity","text":"Gene: nphs2 has been classified as Red List (Low Evidence).","entity_name":"NPHS2","entity_type":"gene"},{"created":"2020-01-03T16:10:19.890729+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FN1 as ready","entity_name":"FN1","entity_type":"gene"},{"created":"2020-01-03T16:10:19.877618+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fn1 has been classified as Green List (High Evidence).","entity_name":"FN1","entity_type":"gene"},{"created":"2020-01-03T16:10:16.626485+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FN1 as Green List (high evidence)","entity_name":"FN1","entity_type":"gene"},{"created":"2020-01-03T16:10:16.611565+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fn1 has been classified as Green List (High Evidence).","entity_name":"FN1","entity_type":"gene"},{"created":"2020-01-03T16:09:58.293165+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.19","user_name":"chirag patel","item_type":"entity","text":"Classified gene: LMX1B as Red List (low evidence)","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-01-03T16:09:58.279095+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.19","user_name":"chirag patel","item_type":"entity","text":"Gene: lmx1b has been classified as Red List (Low Evidence).","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-01-03T16:09:53.924712+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.19","user_name":"chirag patel","item_type":"entity","text":"reviewed gene: NPHS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"NPHS2","entity_type":"gene"},{"created":"2020-01-03T16:09:30.782239+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.19","user_name":"chirag patel","item_type":"entity","text":"Classified gene: CUBN as Red List (low evidence)","entity_name":"CUBN","entity_type":"gene"},{"created":"2020-01-03T16:09:30.759598+11:00","panel_name":"Haematuria_VCGS_KidGen","panel_id":39,"panel_version":"0.19","user_name":"chirag patel","item_type":"entity","text":"Gene: cubn has been classified as Red List (Low Evidence).","entity_name":"CUBN","entity_type":"gene"},{"created":"2020-01-03T16:09:13.531638+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FN1 as Green List (high evidence)","entity_name":"FN1","entity_type":"gene"}]}