{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=593","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=591","results":[{"created":"2023-06-01T20:09:06.893461+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.168","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: PAX7 as ready","entity_name":"PAX7","entity_type":"gene"},{"created":"2023-06-01T20:09:06.877797+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.168","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pax7 has been classified as Green List (High Evidence).","entity_name":"PAX7","entity_type":"gene"},{"created":"2023-06-01T20:08:50.347713+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.168","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PAX7 as Green List (high evidence)","entity_name":"PAX7","entity_type":"gene"},{"created":"2023-06-01T20:08:50.329695+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.168","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pax7 has been classified as Green List (High Evidence).","entity_name":"PAX7","entity_type":"gene"},{"created":"2023-06-01T20:08:03.774126+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.167","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: NEB as ready","entity_name":"NEB","entity_type":"gene"},{"created":"2023-06-01T20:08:03.754889+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.167","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: neb has been classified as Green List (High Evidence).","entity_name":"NEB","entity_type":"gene"},{"created":"2023-06-01T20:07:53.683245+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.167","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: NEB as Green List (high evidence)","entity_name":"NEB","entity_type":"gene"},{"created":"2023-06-01T20:07:53.671529+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.167","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: neb has been classified as Green List (High Evidence).","entity_name":"NEB","entity_type":"gene"},{"created":"2023-06-01T20:07:16.214159+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.166","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MYPN as ready","entity_name":"MYPN","entity_type":"gene"},{"created":"2023-06-01T20:07:16.204002+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.166","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mypn has been classified as Green List (High Evidence).","entity_name":"MYPN","entity_type":"gene"},{"created":"2023-06-01T20:07:12.116061+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.166","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MYPN as Green List (high evidence)","entity_name":"MYPN","entity_type":"gene"},{"created":"2023-06-01T20:07:12.105541+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.166","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mypn has been classified as Green List (High Evidence).","entity_name":"MYPN","entity_type":"gene"},{"created":"2023-06-01T20:06:25.049238+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.165","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MYOD1 as ready","entity_name":"MYOD1","entity_type":"gene"},{"created":"2023-06-01T20:06:25.038141+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.165","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: myod1 has been classified as Green List (High Evidence).","entity_name":"MYOD1","entity_type":"gene"},{"created":"2023-06-01T20:06:01.468857+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.165","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MYOD1 as Green List (high evidence)","entity_name":"MYOD1","entity_type":"gene"},{"created":"2023-06-01T20:06:01.430459+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.165","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: myod1 has been classified as Green List (High Evidence).","entity_name":"MYOD1","entity_type":"gene"},{"created":"2023-06-01T20:04:56.491597+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.164","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MYL1 as ready","entity_name":"MYL1","entity_type":"gene"},{"created":"2023-06-01T20:04:56.479926+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.164","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: myl1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYL1","entity_type":"gene"},{"created":"2023-06-01T20:04:41.334593+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.164","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MYL1 as Amber List (moderate evidence)","entity_name":"MYL1","entity_type":"gene"},{"created":"2023-06-01T20:04:41.327102+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.164","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: myl1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYL1","entity_type":"gene"},{"created":"2023-06-01T20:03:29.158891+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.163","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: MYL1 were set to 30275711","entity_name":"MYL1","entity_type":"gene"},{"created":"2023-06-01T20:01:03.592841+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.162","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MYBPC1 as ready","entity_name":"MYBPC1","entity_type":"gene"},{"created":"2023-06-01T20:01:03.584192+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.162","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mybpc1 has been classified as Green List (High Evidence).","entity_name":"MYBPC1","entity_type":"gene"},{"created":"2023-06-01T20:00:36.583578+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.162","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MYBPC1 as Green List (high evidence)","entity_name":"MYBPC1","entity_type":"gene"},{"created":"2023-06-01T20:00:36.566349+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.162","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mybpc1 has been classified as Green List (High Evidence).","entity_name":"MYBPC1","entity_type":"gene"},{"created":"2023-06-01T19:59:41.033273+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.161","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MTMR14 as ready","entity_name":"MTMR14","entity_type":"gene"},{"created":"2023-06-01T19:59:41.022626+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.161","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mtmr14 has been classified as Amber List (Moderate Evidence).","entity_name":"MTMR14","entity_type":"gene"},{"created":"2023-06-01T19:54:39.757131+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.161","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MTMR14 as Amber List (moderate evidence)","entity_name":"MTMR14","entity_type":"gene"},{"created":"2023-06-01T19:54:39.748831+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.161","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mtmr14 has been classified as Amber List (Moderate Evidence).","entity_name":"MTMR14","entity_type":"gene"},{"created":"2023-06-01T17:37:41.394518+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.928","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFATC1 as ready","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:37:41.385449+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.928","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfatc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:37:31.815399+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.928","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFATC1 as Amber List (moderate evidence)","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:37:31.799761+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.928","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfatc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:37:12.431873+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.927","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NFATC1 was added\ngene: NFATC1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: NFATC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NFATC1 were set to 37249233\nPhenotypes for gene: NFATC1 were set to Inborn error of immunity, MONDO:0003778, NFATC1-related; Combined Immune deficiency\nReview for gene: NFATC1 was set to AMBER\nAdded comment: 3 individuals from a multigenerational consanguineous pedigree with early-onset sinopulmonary infections and bronchiectasis, recurrent viral (warts) and bacterial (folliculitis and abscesses) skin infections, hypogammaglobulinemia, lower CD4+/CD8+ T-cell ratio and lower recent thymic emigrants compared with the age-matched controls. Lymphocyte proliferation responses to PHA and CD3/CD28 stimulations were defective.\r\n\r\nSingle pedigree with supportive functional studies. \nSources: Literature","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:34:29.954601+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFATC1 as ready","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:34:29.946196+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfatc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:34:23.330736+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.39","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFATC1 were changed from Combined Immune deficiency to Inborn error of immunity, MONDO:0003778, NFATC1-related; Combined Immune deficiency","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:32:56.848753+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFATC1 as Amber List (moderate evidence)","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T17:32:56.836605+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfatc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NFATC1","entity_type":"gene"},{"created":"2023-06-01T16:36:39.827637+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.160","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MAP3K20 as ready","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2023-06-01T16:36:39.801906+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.160","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: map3k20 has been classified as Green List (High Evidence).","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2023-06-01T16:36:36.578817+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.160","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MAP3K20 as Green List (high evidence)","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2023-06-01T16:36:36.568144+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.160","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: map3k20 has been classified as Green List (High Evidence).","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2023-06-01T16:35:29.165084+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.159","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: LMOD3 as ready","entity_name":"LMOD3","entity_type":"gene"},{"created":"2023-06-01T16:35:29.154685+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.159","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: lmod3 has been classified as Green List (High Evidence).","entity_name":"LMOD3","entity_type":"gene"},{"created":"2023-06-01T16:35:23.455145+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.159","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: LMOD3 as Green List (high evidence)","entity_name":"LMOD3","entity_type":"gene"},{"created":"2023-06-01T16:35:23.444417+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.159","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: lmod3 has been classified as Green List (High Evidence).","entity_name":"LMOD3","entity_type":"gene"},{"created":"2023-06-01T16:34:36.180780+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.158","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KLHL41 as ready","entity_name":"KLHL41","entity_type":"gene"},{"created":"2023-06-01T16:34:36.167733+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.158","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: klhl41 has been classified as Green List (High Evidence).","entity_name":"KLHL41","entity_type":"gene"},{"created":"2023-06-01T16:33:30.812294+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.158","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KLHL41 as Green List (high evidence)","entity_name":"KLHL41","entity_type":"gene"},{"created":"2023-06-01T16:33:30.804283+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.158","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: klhl41 has been classified as Green List (High Evidence).","entity_name":"KLHL41","entity_type":"gene"},{"created":"2023-06-01T16:32:42.404214+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.157","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KLHL40 as ready","entity_name":"KLHL40","entity_type":"gene"},{"created":"2023-06-01T16:32:42.393628+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.157","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: klhl40 has been classified as Green List (High Evidence).","entity_name":"KLHL40","entity_type":"gene"},{"created":"2023-06-01T16:32:29.239846+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.157","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KLHL40 as Green List (high evidence)","entity_name":"KLHL40","entity_type":"gene"},{"created":"2023-06-01T16:32:29.216279+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.157","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: klhl40 has been classified as Green List (High Evidence).","entity_name":"KLHL40","entity_type":"gene"},{"created":"2023-06-01T16:31:32.267622+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.156","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KBTBD13 as ready","entity_name":"KBTBD13","entity_type":"gene"},{"created":"2023-06-01T16:31:32.233938+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.156","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kbtbd13 has been classified as Green List (High Evidence).","entity_name":"KBTBD13","entity_type":"gene"},{"created":"2023-06-01T16:31:23.884575+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.156","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KBTBD13 as Green List (high evidence)","entity_name":"KBTBD13","entity_type":"gene"},{"created":"2023-06-01T16:31:23.864631+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.156","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kbtbd13 has been classified as Green List (High Evidence).","entity_name":"KBTBD13","entity_type":"gene"},{"created":"2023-06-01T16:30:42.558056+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.155","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: HRAS as ready","entity_name":"HRAS","entity_type":"gene"},{"created":"2023-06-01T16:30:42.543963+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.155","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: hras has been classified as Amber List (Moderate Evidence).","entity_name":"HRAS","entity_type":"gene"},{"created":"2023-06-01T16:30:39.061617+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.155","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: HRAS as Amber List (moderate evidence)","entity_name":"HRAS","entity_type":"gene"},{"created":"2023-06-01T16:30:39.050055+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.155","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: hras has been classified as Amber List (Moderate Evidence).","entity_name":"HRAS","entity_type":"gene"},{"created":"2023-06-01T16:28:48.741836+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.154","user_name":"Sangavi Sivagnanasundram","item_type":"entity","text":"edited their review of gene: EPG5: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:28:23.782920+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.154","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: HACD1 as ready","entity_name":"HACD1","entity_type":"gene"},{"created":"2023-06-01T16:28:23.760379+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.154","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: hacd1 has been classified as Green List (High Evidence).","entity_name":"HACD1","entity_type":"gene"},{"created":"2023-06-01T16:28:17.746551+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.154","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: HACD1 as Green List (high evidence)","entity_name":"HACD1","entity_type":"gene"},{"created":"2023-06-01T16:28:17.735389+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.154","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: hacd1 has been classified as Green List (High Evidence).","entity_name":"HACD1","entity_type":"gene"},{"created":"2023-06-01T16:27:18.502105+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.153","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: FXR1 as ready","entity_name":"FXR1","entity_type":"gene"},{"created":"2023-06-01T16:27:18.488711+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.153","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: fxr1 has been classified as Green List (High Evidence).","entity_name":"FXR1","entity_type":"gene"},{"created":"2023-06-01T16:26:42.405476+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.153","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: FXR1 as Green List (high evidence)","entity_name":"FXR1","entity_type":"gene"},{"created":"2023-06-01T16:26:42.397632+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.153","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: fxr1 has been classified as Green List (High Evidence).","entity_name":"FXR1","entity_type":"gene"},{"created":"2023-06-01T16:25:50.230291+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.152","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: EPG5 as ready","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:25:50.220233+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.152","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: epg5 has been classified as Green List (High Evidence).","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:24:36.146174+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.152","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: EPG5 as Green List (high evidence)","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:24:36.135880+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.152","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: epg5 has been classified as Green List (High Evidence).","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:24:02.747896+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.151","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EPG5 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPG5","entity_type":"gene"},{"created":"2023-06-01T16:16:27.088505+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.150","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: DYNC1H1 as ready","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2023-06-01T16:16:27.077871+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.150","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dync1h1 has been classified as Green List (High Evidence).","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2023-06-01T16:16:19.097457+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.150","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: DYNC1H1 as Green List (high evidence)","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2023-06-01T16:16:19.090016+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.150","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dync1h1 has been classified as Green List (High Evidence).","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2023-06-01T16:15:28.861387+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.149","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: DNM2 as ready","entity_name":"DNM2","entity_type":"gene"},{"created":"2023-06-01T16:15:28.847953+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.149","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dnm2 has been classified as Green List (High Evidence).","entity_name":"DNM2","entity_type":"gene"},{"created":"2023-06-01T16:14:53.075502+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.149","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: DNM2 as Green List (high evidence)","entity_name":"DNM2","entity_type":"gene"},{"created":"2023-06-01T16:14:53.066267+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.149","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dnm2 has been classified as Green List (High Evidence).","entity_name":"DNM2","entity_type":"gene"},{"created":"2023-06-01T16:14:14.485888+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.148","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: DHX16 as ready","entity_name":"DHX16","entity_type":"gene"},{"created":"2023-06-01T16:14:14.468963+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.148","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dhx16 has been classified as Red List (Low Evidence).","entity_name":"DHX16","entity_type":"gene"},{"created":"2023-06-01T16:14:07.235444+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.148","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: DHX16 as Red List (low evidence)","entity_name":"DHX16","entity_type":"gene"},{"created":"2023-06-01T16:14:07.207571+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.148","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dhx16 has been classified as Red List (Low Evidence).","entity_name":"DHX16","entity_type":"gene"},{"created":"2023-06-01T16:10:32.917588+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.926","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: CNTN1 were changed from Myopathy, congenital, Compton-North 612540 to Compton-North congenital myopathy MONDO:0012929; fetal akinesia deformation sequence MONDO:0008824","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:10:31.228333+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.147","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: CNTN1 as ready","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:10:31.184756+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.147","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: cntn1 has been classified as Amber List (Moderate Evidence).","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:10:30.897163+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.147","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: CNTN1 as Amber List (moderate evidence)","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:10:30.887872+10:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.147","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: cntn1 has been classified as Amber List (Moderate Evidence).","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:09:59.003693+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.925","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: CNTN1 were set to 19026398","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:09:43.719443+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.924","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: CNTN1 as Green List (high evidence)","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:09:43.701982+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.924","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: cntn1 has been classified as Green List (High Evidence).","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T16:09:23.944142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.923","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: CNTN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19026398, 10595523, 22242131, 32779773; Phenotypes: Compton-North congenital myopathy MONDO:0012929, fetal akinesia deformation sequence MONDO:0008824; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNTN1","entity_type":"gene"},{"created":"2023-06-01T15:09:01.930858+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2175","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDP1 as ready","entity_name":"PDP1","entity_type":"gene"},{"created":"2023-06-01T15:09:01.917670+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdp1 has been classified as Green List (High Evidence).","entity_name":"PDP1","entity_type":"gene"}]}