{"count":220489,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1275","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1273","results":[{"created":"2021-07-07T18:34:30.883251+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.448","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR60 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR60","entity_type":"gene"},{"created":"2021-07-07T18:33:55.223823+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.447","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR60: Rating: GREEN; Mode of pathogenicity: None; Publications: 23910462, 29271569, 26874042; Phenotypes: Short-rib thoracic dysplasia 8 with or without polydactyly, MIM# 615503, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR60","entity_type":"gene"},{"created":"2021-07-07T18:30:45.475296+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.447","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR34 as ready","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:30:45.411518+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.447","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr34 has been classified as Green List (High Evidence).","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:27:37.323490+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.447","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR34 were changed from  to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Retinitis pigmentosa","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:27:15.838989+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR34 as ready","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:27:15.816210+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr34 has been classified as Red List (Low Evidence).","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:27:05.375955+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR34 was added\ngene: WDR34 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Literature\nMode of inheritance for gene: WDR34 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WDR34 were set to 33124039\nPhenotypes for gene: WDR34 were set to Retinitis pigmentosa\nReview for gene: WDR34 was set to RED\nAdded comment: Single case report of association with RP. Gene-disease association well established for skeletal ciliopathy. \nSources: Literature","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:25:30.434566+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR34 as ready","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:25:30.421802+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr34 has been classified as Green List (High Evidence).","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:25:28.022053+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR34 were changed from  to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:25:02.775001+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR34 were set to ","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:24:34.488374+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:24:10.910444+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:23:17.917478+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8254","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR34 as ready","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:23:17.905914+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8254","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr34 has been classified as Green List (High Evidence).","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:23:10.131608+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8254","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR34 were changed from  to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Retinitis pigmentosa","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:22:50.643954+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8253","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR34 were set to ","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:22:30.637473+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8252","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:22:12.508213+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8251","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 33124039, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:22:11.744932+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.446","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR34 were set to ","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:21:32.927156+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.445","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:21:04.256830+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.444","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 33124039, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-07-07T18:04:55.863672+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8251","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR19 as ready","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:04:55.852751+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8251","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr19 has been classified as Green List (High Evidence).","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:04:48.014915+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8251","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR19 were changed from  to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:04:30.350255+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8250","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR19 were set to ","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:04:13.186070+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8249","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:03:54.208461+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8248","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR19: Rating: GREEN; Mode of pathogenicity: None; Publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:03:04.655371+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.444","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR19 as ready","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:03:04.644836+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.444","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr19 has been classified as Green List (High Evidence).","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:02:55.242874+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.444","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR19 were changed from  to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:02:15.343779+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.443","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR19 were set to ","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:01:51.846944+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.442","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T18:01:17.393857+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.441","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR19: Rating: GREEN; Mode of pathogenicity: None; Publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-07-07T17:57:17.190486+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TXNDC15 as ready","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:57:17.181331+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: txndc15 has been classified as Green List (High Evidence).","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:57:15.042528+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TXNDC15 were changed from  to Meckel-Gruber syndrome","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:56:52.054189+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TXNDC15 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:56:33.315498+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.192","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TXNDC15 were set to ","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:56:11.860323+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.192","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TXNDC15 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:55:47.477964+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.191","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:55:43.854953+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8248","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TXNDC15 as ready","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:55:43.844319+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8248","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: txndc15 has been classified as Green List (High Evidence).","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:55:27.495606+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8248","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TXNDC15 were changed from  to Meckel-Gruber syndrome","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:54:52.225696+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TXNDC15: Rating: GREEN; Mode of pathogenicity: None; Publications: 30851085, 27894351; Phenotypes: Meckel-Gruber syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:54:43.133446+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8247","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TXNDC15 were set to ","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:53:42.258172+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8246","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:53:25.293511+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8245","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TXNDC15: Rating: GREEN; Mode of pathogenicity: None; Publications: 30851085, 27894351; Phenotypes: Meckel-Gruber syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:52:26.841645+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.441","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TXNDC15 as ready","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:52:26.829269+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.441","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: txndc15 has been classified as Green List (High Evidence).","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:52:15.352657+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.441","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TXNDC15 were changed from  to Meckel-Gruber syndrome","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:51:47.398584+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.440","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TXNDC15 were set to ","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:51:19.612715+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.439","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TXNDC15","entity_type":"gene"},{"created":"2021-07-07T17:49:54.191661+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3933","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:49:54.181531+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3933","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:49:49.246154+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3933","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from  to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:49:15.749337+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3932","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:48:49.117457+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3931","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:48:19.364255+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3930","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 14520415, 19797195; Phenotypes: Bardet-Biedl syndrome 8, MIM# 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:47:45.748621+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:47:45.734448+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:47:42.828164+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from  to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:47:18.703600+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:46:33.195831+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8245","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:46:33.183619+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8245","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:46:26.136083+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8245","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from  to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:45:58.837317+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8244","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:45:40.588095+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8243","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:45:22.711418+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8242","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 14520415, 19797195; Phenotypes: Bardet-Biedl syndrome 8, MIM# 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:44:28.196583+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.438","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:44:28.185602+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.438","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:44:25.944673+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.438","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from  to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:44:01.807657+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.437","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:43:32.325122+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-07-07T17:42:33.841474+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC21B as ready","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:42:33.831803+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Green List (High Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:42:23.111009+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC21B were changed from Bardet-Biedl syndrome to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:42:12.677153+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.249","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC21B were set to ","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:42:02.398054+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TTC21B as Green List (high evidence)","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:42:02.388201+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Green List (High Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:41:50.569933+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.247","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC21B: Rating: GREEN; Mode of pathogenicity: None; Publications: 21258341, 25492405, 18327258, 33875766; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:41:04.930655+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.355","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC21B as ready","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:41:04.912253+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.355","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Red List (Low Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:41:02.147389+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.355","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC21B were changed from  to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:40:38.073220+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.354","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:40:19.539479+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.353","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TTC21B as Red List (low evidence)","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:40:19.529323+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.353","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Red List (Low Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:39:55.977174+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.352","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC21B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819, Joubert syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:38:44.116643+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8242","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC21B as ready","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:38:44.098081+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8242","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Green List (High Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:38:28.809637+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8242","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC21B were changed from  to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:38:05.516601+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8241","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC21B were set to ","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:37:47.480877+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8240","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:37:29.786900+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8239","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC21B: Rating: GREEN; Mode of pathogenicity: None; Publications: 21258341, 25492405, 18327258, 33875766; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819, Joubert syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:36:22.621610+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC21B as ready","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:36:22.612995+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Green List (High Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:36:19.437774+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC21B were changed from  to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:35:41.338960+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.434","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC21B were set to ","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-07-07T17:35:15.245497+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"}]}