{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1779","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1777","results":[{"created":"2020-06-01T20:04:54.485831+10:00","panel_name":"Long QT Syndrome","panel_id":131,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNJ5 as Red List (low evidence)","entity_name":"KCNJ5","entity_type":"gene"},{"created":"2020-06-01T20:04:54.476755+10:00","panel_name":"Long QT Syndrome","panel_id":131,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj5 has been classified as Red List (Low Evidence).","entity_name":"KCNJ5","entity_type":"gene"},{"created":"2020-06-01T20:02:53.404391+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPHP4 as ready","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:02:53.394058+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nphp4 has been classified as Amber List (Moderate Evidence).","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:02:53.041998+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPHP4 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:02:32.646097+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPHP4 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:02:01.289733+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPHP4 as Amber List (moderate evidence)","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:02:01.276181+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nphp4 has been classified as Amber List (Moderate Evidence).","entity_name":"NPHP4","entity_type":"gene"},{"created":"2020-06-01T20:00:19.542577+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX2-5 as ready","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T20:00:19.533735+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-5 has been classified as Green List (High Evidence).","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T20:00:05.660837+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NKX2-5 were changed from  to Ventricular septal defect 3 (MIM#614432); Tetralogy of Fallot (MIM#187500)","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T19:59:17.336656+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NKX2-5 were set to ","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T19:58:54.480745+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NKX2-5 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T19:58:34.342771+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NKX2-5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2020-06-01T19:05:14.872578+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCNO as ready","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:05:14.862336+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccno has been classified as Red List (Low Evidence).","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:05:11.631823+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCNO were changed from  to Ciliary dyskinesia, primary, 29, MIM# 615872","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:04:40.300840+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCNO were set to ","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:04:11.506741+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCNO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:03:44.862715+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCNO as Red List (low evidence)","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T19:03:44.853713+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccno has been classified as Red List (Low Evidence).","entity_name":"CCNO","entity_type":"gene"},{"created":"2020-06-01T18:41:36.780163+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CRELD1 as Amber List (moderate evidence)","entity_name":"CRELD1","entity_type":"gene"},{"created":"2020-06-01T18:41:36.767285+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: creld1 has been classified as Amber List (Moderate Evidence).","entity_name":"CRELD1","entity_type":"gene"},{"created":"2020-06-01T18:41:06.044466+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three families reported with heterozygous missense variants and heterotaxy phenotype. \nSources: Expert list; to: Three families reported with heterozygous missense variants and heterotaxy phenotype. However, supporting evidence of pathogenicity for some of the variants is relatively weak.\r\nSources: Expert list","entity_name":"CRELD1","entity_type":"gene"},{"created":"2020-06-01T18:40:39.966850+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CRELD1: Changed rating: AMBER","entity_name":"CRELD1","entity_type":"gene"},{"created":"2020-06-01T18:35:47.892945+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF2 as ready","entity_name":"DNAAF2","entity_type":"gene"},{"created":"2020-06-01T18:35:47.881053+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf2 has been classified as Green List (High Evidence).","entity_name":"DNAAF2","entity_type":"gene"},{"created":"2020-06-01T18:35:44.698983+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF2 were changed from  to Ciliary dyskinesia, primary, 10 612518","entity_name":"DNAAF2","entity_type":"gene"},{"created":"2020-06-01T18:35:17.106820+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF2 were set to ","entity_name":"DNAAF2","entity_type":"gene"},{"created":"2020-06-01T18:34:54.118475+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF2","entity_type":"gene"},{"created":"2020-06-01T18:29:54.173823+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH1 as ready","entity_name":"DNAH1","entity_type":"gene"},{"created":"2020-06-01T18:29:54.163692+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah1 has been classified as Red List (Low Evidence).","entity_name":"DNAH1","entity_type":"gene"},{"created":"2020-06-01T18:29:48.608264+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAH1 as Red List (low evidence)","entity_name":"DNAH1","entity_type":"gene"},{"created":"2020-06-01T18:29:48.599245+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah1 has been classified as Red List (Low Evidence).","entity_name":"DNAH1","entity_type":"gene"},{"created":"2020-06-01T18:26:32.368163+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2985","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH6 as ready","entity_name":"DNAH6","entity_type":"gene"},{"created":"2020-06-01T18:26:32.354415+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2985","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah6 has been classified as Amber List (Moderate Evidence).","entity_name":"DNAH6","entity_type":"gene"},{"created":"2020-06-01T18:25:55.947062+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2985","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAH6 as Amber List (moderate evidence)","entity_name":"DNAH6","entity_type":"gene"},{"created":"2020-06-01T18:25:55.937628+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2985","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah6 has been classified as Amber List (Moderate Evidence).","entity_name":"DNAH6","entity_type":"gene"},{"created":"2020-06-01T18:25:10.663478+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH9 as ready","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:25:10.648764+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah9 has been classified as Green List (High Evidence).","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:25:03.168137+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH9 were changed from  to Ciliary dyskinesia, primary, 40, MIM# 618300","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:24:38.831049+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH9 were set to ","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:24:14.018183+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAH9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:23:44.082704+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAH9: Rating: GREEN; Mode of pathogenicity: None; Publications: 30471717, 30471718; Phenotypes: Ciliary dyskinesia, primary, 40, MIM# 618300; Mode of inheritance: None","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:21:57.716543+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH9 as ready","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:21:57.706106+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah9 has been classified as Green List (High Evidence).","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:21:51.844098+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAH9 as Green List (high evidence)","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:21:51.835051+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah9 has been classified as Green List (High Evidence).","entity_name":"DNAH9","entity_type":"gene"},{"created":"2020-06-01T18:18:07.570732+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2984","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DRC1 as ready","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:18:07.562084+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2984","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drc1 has been classified as Green List (High Evidence).","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:17:58.422717+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2984","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DRC1 were changed from  to Ciliary dyskinesia, primary, 21, MIM# 615294","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:17:34.348375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2983","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DRC1 were set to ","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:17:14.834847+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2982","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DRC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:16:57.005043+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2981","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: DRC1.","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:16:45.549093+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2981","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DRC1: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:16:34.038058+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2981","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DRC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 31960620; Phenotypes: Ciliary dyskinesia, primary, 21, MIM# 615294; Mode of inheritance: None","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:14:56.398728+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DRC1 as ready","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:14:56.386725+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drc1 has been classified as Red List (Low Evidence).","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:14:53.608376+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DRC1 were changed from  to Ciliary dyskinesia, primary, 21, MIM# 615294","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:13:16.081581+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DRC1 were set to ","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:12:47.103334+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DRC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:10:30.975398+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DRC1 as Red List (low evidence)","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:10:30.965820+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drc1 has been classified as Red List (Low Evidence).","entity_name":"DRC1","entity_type":"gene"},{"created":"2020-06-01T18:07:51.084397+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TLL1 as ready","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:07:51.073380+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tll1 has been classified as Green List (High Evidence).","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:07:47.953541+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TLL1 were set to ","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:06:58.779572+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TLL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:06:25.166485+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TLL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18830233, 30538173, 27418595, 31570783; Phenotypes: Atrial septal defect; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:05:29.256026+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2981","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TLL1 were changed from  to Atrial septal defect","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:05:07.571011+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2980","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TLL1 were set to ","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T18:04:05.572941+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2979","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TLL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T17:52:47.873553+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2978","user_name":"Dean Phelan","item_type":"entity","text":"reviewed gene: TLL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18830233, 30538173, 27418595, 31570783; Phenotypes: Atrial septal defect; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TLL1","entity_type":"gene"},{"created":"2020-06-01T16:58:07.821814+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2978","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HIST1H4J as ready","entity_name":"HIST1H4J","entity_type":"gene"},{"created":"2020-06-01T16:58:07.811677+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2978","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hist1h4j has been classified as Amber List (Moderate Evidence).","entity_name":"HIST1H4J","entity_type":"gene"},{"created":"2020-06-01T16:57:59.374169+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2978","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HIST1H4J as Amber List (moderate evidence)","entity_name":"HIST1H4J","entity_type":"gene"},{"created":"2020-06-01T16:57:59.360931+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2978","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hist1h4j has been classified as Amber List (Moderate Evidence).","entity_name":"HIST1H4J","entity_type":"gene"},{"created":"2020-06-01T16:57:41.431953+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2977","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HIST1H4J was added\ngene: HIST1H4J was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: HIST1H4J was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: HIST1H4J were set to 31804630\nPhenotypes for gene: HIST1H4J were set to microcephaly; intellectual disability; dysmorphic features\nReview for gene: HIST1H4J was set to AMBER\nAdded comment: Single case report but with functional evidence in zebrafish and phenotypic similarity to other HIST1H4C phenotype \nSources: Literature","entity_name":"HIST1H4J","entity_type":"gene"},{"created":"2020-06-01T16:55:13.799529+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2976","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCIDAS as ready","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:55:13.790691+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2976","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcidas has been classified as Green List (High Evidence).","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:55:06.701014+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2976","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCIDAS were changed from  to Ciliary dyskinesia, primary, 42 (MIM#618695)","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:54:44.259956+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2975","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCIDAS were set to ","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:54:07.430642+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2974","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MCIDAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:53:48.433087+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2973","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MCIDAS: Rating: GREEN; Mode of pathogenicity: None; Publications: 25048963; Phenotypes: Ciliary dyskinesia, primary, 42 (MIM#618695); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:52:39.201777+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCIDAS as ready","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:52:39.187979+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcidas has been classified as Red List (Low Evidence).","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:52:36.591888+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCIDAS were changed from  to Ciliary dyskinesia, primary, 42 (MIM#618695)","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:51:53.500041+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCIDAS were set to ","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:50:30.783165+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MCIDAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:50:02.281923+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MCIDAS as Red List (low evidence)","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:50:02.272719+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcidas has been classified as Red List (Low Evidence).","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:49:24.609961+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCIDAS as ready","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:49:24.601307+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcidas has been classified as Green List (High Evidence).","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:47:28.611180+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCIDAS were changed from  to Ciliary dyskinesia, primary, 42 (MIM#618695)","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:45:43.063023+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCIDAS were set to ","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:45:10.172810+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MCIDAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCIDAS","entity_type":"gene"},{"created":"2020-06-01T16:36:15.236372+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2973","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VWA3B as ready","entity_name":"VWA3B","entity_type":"gene"},{"created":"2020-06-01T16:36:15.225119+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2973","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vwa3b has been classified as Red List (Low Evidence).","entity_name":"VWA3B","entity_type":"gene"},{"created":"2020-06-01T16:33:07.500750+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOR1AIP1 as ready","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2020-06-01T16:33:07.491531+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1aip1 has been classified as Green List (High Evidence).","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2020-06-01T16:33:03.330980+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOR1AIP1 as Green List (high evidence)","entity_name":"TOR1AIP1","entity_type":"gene"}]}