{"count":220486,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1279","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1277","results":[{"created":"2021-07-04T15:28:48.920694+10:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IQCB1 were set to ","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:28:37.074548+10:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254, MONDO:0012225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:28:04.215217+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQCB1 as ready","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:28:04.188885+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqcb1 has been classified as Green List (High Evidence).","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:27:56.819697+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.181","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IQCB1 were changed from  to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:27:33.044244+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.180","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IQCB1 were set to ","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:27:09.371390+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:26:38.918768+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254, MONDO:0012225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:25:48.674295+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8195","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQCB1 as ready","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:25:48.665004+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8195","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqcb1 has been classified as Green List (High Evidence).","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:25:40.375989+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8195","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IQCB1 were changed from  to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:25:23.310906+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8194","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IQCB1 were set to ","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:25:05.914014+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8193","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:24:39.348610+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8192","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254, MONDO:0012225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:24:22.054698+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.395","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IQCB1 were changed from Senior-Loken syndrome 5, MIM# 609254 to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:23:30.232107+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.394","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQCB1 as ready","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:23:30.221637+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.394","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqcb1 has been classified as Green List (High Evidence).","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:23:27.858217+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.394","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IQCB1 were changed from  to Senior-Loken syndrome 5, MIM# 609254","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:23:04.148380+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.393","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IQCB1 were set to ","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:22:46.899318+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.392","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:21:58.017509+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IQCB1","entity_type":"gene"},{"created":"2021-07-04T15:18:36.239164+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HNF1B as ready","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:18:36.229349+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnf1b has been classified as Green List (High Evidence).","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:18:32.218657+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HNF1B were changed from  to Renal cysts and diabetes syndrome, MIM# 137920","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:18:03.568376+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.390","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HNF1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:17:39.590274+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: HNF1B.","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:17:30.863542+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.389","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HNF1B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal cysts and diabetes syndrome, MIM# 137920; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HNF1B","entity_type":"gene"},{"created":"2021-07-04T15:16:20.843980+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT80 as ready","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:16:20.828840+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift80 has been classified as Green List (High Evidence).","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:16:18.573691+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT80 were changed from  to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:15:56.472316+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT80 were set to ","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:15:32.397542+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:15:06.700050+10:00","panel_name":"Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy","panel_id":179,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263, MONDO:0012644; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:14:08.175129+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8192","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT80 as ready","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:14:08.163833+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8192","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift80 has been classified as Green List (High Evidence).","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:14:00.823106+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8192","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT80 were changed from  to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:13:42.526244+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8191","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT80 were set to ","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:13:22.861320+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8190","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:13:04.970948+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8189","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: IFT80: 5 unrelated families reported.","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:12:58.390949+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8189","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263, MONDO:0012644; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:12:33.551254+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.389","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT80 were changed from Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263 to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:11:22.830708+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.388","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT80 as ready","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:11:22.818438+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.388","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift80 has been classified as Green List (High Evidence).","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:11:12.631165+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.388","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT80 were changed from  to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:10:48.128680+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.387","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT80 were set to ","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:10:20.447294+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:09:56.453749+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.385","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2021-07-04T15:00:04.414617+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8189","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T15:00:04.400689+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8189","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:59:57.334637+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from  to Bardet-Biedl syndrome 17 (MIM#615994)","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:59:39.111783+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8188","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:59:05.256004+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8187","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:54:34.594780+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LZTFL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22510444, 23692385, 27312011, 22072986; Phenotypes: Bardet-Biedl syndrome 17 (MIM#615994); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:53:27.921815+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.385","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:53:27.911416+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.385","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:53:25.528101+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.385","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from  to Bardet-Biedl syndrome 17 (MIM#615994)","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:52:58.973934+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.384","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:52:35.515043+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.383","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2021-07-04T14:50:42.950040+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.382","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LBR as ready","entity_name":"LBR","entity_type":"gene"},{"created":"2021-07-04T14:50:42.937208+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.382","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lbr has been classified as Green List (High Evidence).","entity_name":"LBR","entity_type":"gene"},{"created":"2021-07-04T14:50:40.622288+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.382","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LBR were changed from  to Greenberg skeletal dysplasia, MIM#215140","entity_name":"LBR","entity_type":"gene"},{"created":"2021-07-04T14:50:16.056098+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.381","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LBR were set to ","entity_name":"LBR","entity_type":"gene"},{"created":"2021-07-04T14:49:56.477808+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.380","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LBR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LBR","entity_type":"gene"},{"created":"2021-07-04T14:47:23.747097+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Seven families and functional data including zebrafish model. \r\nSources: Literature; to: Nine families and functional data including zebrafish model. \r\nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:47:10.643222+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three unrelated families and functional data including zebrafish model. \nSources: Literature; to: Seven families and functional data including zebrafish model. \r\nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:46:48.389440+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three unrelated families and functional data including zebrafish model. Cholestasis prominent. \nSources: Literature; to: 7 families and functional data including zebrafish model. Cholestasis prominent. \r\nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:46:37.827953+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC26 as ready","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:46:37.818390+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:46:26.063550+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three unrelated families and functional data including zebrafish model. \nSources: Literature; to: 9 families and functional data including zebrafish model. \r\nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:44:56.101466+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TTC26 as Green List (high evidence)","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:44:56.092364+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:44:24.300854+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC26 was added\ngene: TTC26 was added to Cholestasis. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. Cholestasis prominent. \nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:43:04.754704+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC26 as ready","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:43:04.741943+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:42:56.205108+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TTC26 as Green List (high evidence)","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:42:56.195342+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8186","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:42:23.738061+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8185","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC26 was added\ngene: TTC26 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. \nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:40:43.360012+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC26 as ready","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:40:43.349887+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:40:37.880010+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TTC26 as Green List (high evidence)","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:40:37.870659+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.379","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc26 has been classified as Green List (High Evidence).","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:39:25.535777+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.378","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC26 was added\ngene: TTC26 was added to Ciliopathies. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. \nSources: Literature","entity_name":"TTC26","entity_type":"gene"},{"created":"2021-07-04T14:34:16.051207+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.377","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF7 as ready","entity_name":"KIF7","entity_type":"gene"},{"created":"2021-07-04T14:34:16.008657+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.377","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif7 has been classified as Green List (High Evidence).","entity_name":"KIF7","entity_type":"gene"},{"created":"2021-07-04T14:34:12.916994+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.377","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF7 were changed from  to Joubert syndrome 12, MIM# 200990; Acrocallosal syndrome, MIM# 200990; MONDO:0008708; Hydrolethalus syndrome 2, MIM# 614120","entity_name":"KIF7","entity_type":"gene"},{"created":"2021-07-04T14:33:38.634072+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.376","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF7 were set to ","entity_name":"KIF7","entity_type":"gene"},{"created":"2021-07-04T14:33:16.722538+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.375","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIF7","entity_type":"gene"},{"created":"2021-07-04T14:32:04.840370+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.374","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIAA0753 as ready","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:32:04.828496+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.374","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa0753 has been classified as Green List (High Evidence).","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:32:01.690075+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.374","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIAA0753 were changed from  to Orofaciodigital syndrome XV 617127; Joubert syndrome","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:31:36.998270+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.373","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIAA0753 were set to ","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:31:07.754396+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.372","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIAA0753 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:30:40.223785+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"KIAA0753","entity_type":"gene"},{"created":"2021-07-04T14:29:51.881583+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIAA0586 as ready","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:29:51.871914+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa0586 has been classified as Green List (High Evidence).","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:29:49.180712+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIAA0586 were changed from  to Joubert syndrome 23 616490; Short-rib thoracic dysplasia 14 with polydactyly 616546","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:29:19.885170+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.370","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIAA0586 were set to ","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:28:50.031604+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.369","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KIAA0586: Changed rating: GREEN; Changed publications: 26166481; Changed phenotypes: Short-rib thoracic dysplasia 14 with polydactyly, MIM# 616546; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:27:38.231214+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.369","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIAA0586 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2021-07-04T14:27:16.367493+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: KIAA0586.","entity_name":"KIAA0586","entity_type":"gene"}]}