{"count":220465,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1285","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1283","results":[{"created":"2021-06-26T12:54:11.910680+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS7 as ready","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:54:11.898334+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs7 has been classified as Green List (High Evidence).","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:54:09.356229+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS7 were changed from  to Bardet-Biedl syndrome 7, MIM# 615984; MONDO:0014435","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:53:43.909521+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.317","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS7 were set to ","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:53:20.534890+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:52:53.294479+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBS7: Changed phenotypes: Bardet-Biedl syndrome 7, MIM# 615984, MONDO:0014435","entity_name":"BBS7","entity_type":"gene"},{"created":"2021-06-26T12:51:53.794183+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.204","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS5 as ready","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:51:53.784225+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.204","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs5 has been classified as Green List (High Evidence).","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:51:50.872873+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.204","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from  to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:51:26.626807+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.203","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS5 were set to ","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:50:52.641130+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, polydactyly is a feature.","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:50:29.616200+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, renal abnormalities are a feature.","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:49:53.226085+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS5 as ready","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:49:53.216792+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs5 has been classified as Green List (High Evidence).","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:49:50.578297+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from  to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:49:27.624760+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS5 were set to ","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:48:58.018930+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:48:33.885650+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:48:01.122168+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3901","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS5 as ready","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:48:01.112669+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3901","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs5 has been classified as Green List (High Evidence).","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:47:57.447056+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3901","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from  to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:47:33.180564+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3900","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS5 were set to ","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:47:00.278717+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3899","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-26T12:46:19.918474+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3898","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:27:02.612905+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8121","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS5 as ready","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:27:02.603359+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8121","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs5 has been classified as Green List (High Evidence).","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:26:55.238138+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from  to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:26:35.555556+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8120","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS5 were set to ","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:26:15.228631+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8119","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:25:57.587276+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8118","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:25:12.299122+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.3","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from Bardet-Biedl syndrome 5, MIM#615983 to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:24:38.809605+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBS5: Changed phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:24:12.181815+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS5 as ready","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:24:12.168140+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs5 has been classified as Green List (High Evidence).","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:24:08.288554+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS5 were changed from  to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:23:38.574462+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.314","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS5 were set to ","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:23:02.384181+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:22:32.277268+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBS5: Changed phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434","entity_name":"BBS5","entity_type":"gene"},{"created":"2021-06-25T19:17:38.946428+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3898","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS4 as ready","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:17:38.932992+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3898","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs4 has been classified as Green List (High Evidence).","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:17:34.318467+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3898","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from  to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:17:06.614350+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3897","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS4 were set to ","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:16:45.886552+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3896","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:15:45.308510+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3895","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:14:58.093857+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS4 as ready","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:14:58.081528+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs4 has been classified as Green List (High Evidence).","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:14:55.420478+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from  to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:14:26.913899+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS4 were set to ","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:14:07.979234+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:13:36.268612+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:12:23.236428+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS4 as ready","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:12:23.226628+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs4 has been classified as Green List (High Evidence).","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:12:11.701183+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from  to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:11:34.496145+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS4 were set to ","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:01:33.958918+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS4 as ready","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:01:33.947881+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs4 has been classified as Green List (High Evidence).","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:00:40.056290+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from  to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T19:00:16.857119+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8117","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS4 were set to ","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:59:55.294109+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:59:35.751701+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8115","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:58:57.280529+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from Bardet-Biedl syndrome 4, MIM#615982 to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:58:13.084203+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS4 as ready","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:58:13.073724+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs4 has been classified as Green List (High Evidence).","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:58:08.991501+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS4 were changed from  to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:57:38.816260+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.311","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS4 were set to ","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:57:10.127729+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T18:56:41.057181+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBS4: Changed phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433","entity_name":"BBS4","entity_type":"gene"},{"created":"2021-06-25T17:59:31.004429+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS2 as ready","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:59:30.991365+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs2 has been classified as Green List (High Evidence).","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:58:53.625640+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS2 were changed from  to Bardet-Biedl syndrome 2, MIM# 615981; Retinitis pigmentosa 74, MIM# 616562","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:56:45.159558+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.308","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS2 were set to ","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:56:18.682367+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:55:49.202417+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association. Limited number of families also reported with isolated RP.","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:55:32.910643+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBS2: Changed publications: 11567139, 16823392, 28143435, 31960602, 25541840; Changed phenotypes: Bardet-Biedl syndrome 2, MIM# 615981, Retinitis pigmentosa 74, MIM# 616562","entity_name":"BBS2","entity_type":"gene"},{"created":"2021-06-25T17:53:27.948690+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS12 as ready","entity_name":"BBS12","entity_type":"gene"},{"created":"2021-06-25T17:53:27.936812+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs12 has been classified as Green List (High Evidence).","entity_name":"BBS12","entity_type":"gene"},{"created":"2021-06-25T17:52:57.414853+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS12 were changed from  to Bardet-Biedl syndrome 12, MIM# 615989","entity_name":"BBS12","entity_type":"gene"},{"created":"2021-06-25T17:52:33.171996+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS12 were set to ","entity_name":"BBS12","entity_type":"gene"},{"created":"2021-06-25T17:52:04.198951+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS12","entity_type":"gene"},{"created":"2021-06-25T17:51:26.797193+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARL6 as ready","entity_name":"ARL6","entity_type":"gene"},{"created":"2021-06-25T17:51:26.787083+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arl6 has been classified as Green List (High Evidence).","entity_name":"ARL6","entity_type":"gene"},{"created":"2021-06-25T15:04:22.591586+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS10 as ready","entity_name":"BBS10","entity_type":"gene"},{"created":"2021-06-25T15:04:22.580527+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs10 has been classified as Green List (High Evidence).","entity_name":"BBS10","entity_type":"gene"},{"created":"2021-06-25T14:55:39.108966+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS10 were changed from  to Bardet-Biedl syndrome 10, MIM# 615987","entity_name":"BBS10","entity_type":"gene"},{"created":"2021-06-25T14:55:14.508417+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.302","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS10 were set to ","entity_name":"BBS10","entity_type":"gene"},{"created":"2021-06-25T14:54:43.100416+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS10","entity_type":"gene"},{"created":"2021-06-25T14:54:06.236747+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS1 as ready","entity_name":"BBS1","entity_type":"gene"},{"created":"2021-06-25T14:54:06.224602+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs1 has been classified as Green List (High Evidence).","entity_name":"BBS1","entity_type":"gene"},{"created":"2021-06-25T14:54:02.500805+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS1 were changed from  to Bardet-Biedl syndrome 1, MIM# 209900","entity_name":"BBS1","entity_type":"gene"},{"created":"2021-06-25T14:53:29.342336+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS1 were set to ","entity_name":"BBS1","entity_type":"gene"},{"created":"2021-06-25T14:52:25.727303+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS1","entity_type":"gene"},{"created":"2021-06-25T14:51:41.484879+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B9D2 as ready","entity_name":"B9D2","entity_type":"gene"},{"created":"2021-06-25T14:51:41.470288+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d2 has been classified as Green List (High Evidence).","entity_name":"B9D2","entity_type":"gene"},{"created":"2021-06-25T14:51:38.472541+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B9D2 were changed from  to Joubert syndrome 34, MIM# 614175; Meckel syndrome 10, MIM# 614175","entity_name":"B9D2","entity_type":"gene"},{"created":"2021-06-25T14:51:08.399371+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.296","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B9D2 were set to ","entity_name":"B9D2","entity_type":"gene"},{"created":"2021-06-25T14:50:51.125877+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.295","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B9D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D2","entity_type":"gene"},{"created":"2021-06-25T14:48:15.960626+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARL6 as ready","entity_name":"ARL6","entity_type":"gene"},{"created":"2021-06-25T14:48:15.950014+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arl6 has been classified as Green List (High Evidence).","entity_name":"ARL6","entity_type":"gene"},{"created":"2021-06-25T14:48:13.581956+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARL6 were changed from  to Bardet-Biedl syndrome 3, MIM# 600151","entity_name":"ARL6","entity_type":"gene"},{"created":"2021-06-25T14:47:42.437173+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARL6 were set to ","entity_name":"ARL6","entity_type":"gene"}]}