{"count":220249,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=887","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=885","results":[{"created":"2022-04-11T08:56:06.486188+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12830","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A15 were changed from  to Hyperornithinaemia-hyperammonaemia-homocitrullinaemia syndrome , MIM#238970","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2022-04-11T08:55:38.523122+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12829","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A15 were set to ","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2022-04-11T08:55:14.039658+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12828","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2022-04-11T08:54:15.599006+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12827","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC25A15: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369256, 19242930]; Phenotypes: Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome , MIM#238970; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2022-04-09T17:48:47.493399+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12827","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A19 as ready","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:48:47.483021+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12827","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a19 has been classified as Green List (High Evidence).","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:47:20.383646+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12827","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A19 were changed from  to Microcephaly, Amish type, MIM#607196; Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), MIM#613710","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:46:59.308461+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12826","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A19 were set to ","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:46:20.305208+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12825","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:45:59.382529+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12824","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC25A19: Rating: GREEN; Mode of pathogenicity: None; Publications: 31506564, 31295743, 12185364, 19798730; Phenotypes: Microcephaly, Amish type, MIM#607196, Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), MIM#613710; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2022-04-09T17:44:55.648133+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A22 as ready","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:44:55.634833+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a22 has been classified as Green List (High Evidence).","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:44:32.656805+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A22 were changed from  to Developmental and epileptic encephalopathy 3, MIM# 609304","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:44:00.333483+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1551","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A22 were set to ","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:43:57.641069+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12824","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A22 as ready","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:43:57.625954+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12824","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a22 has been classified as Green List (High Evidence).","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:43:49.009143+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12824","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A22 were changed from  to Developmental and epileptic encephalopathy 3, MIM# 609304","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:43:29.440493+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12823","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A22 were set to ","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:43:29.084451+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1550","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A22 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:42:50.909916+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1549","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC25A22: Rating: GREEN; Mode of pathogenicity: None; Publications: 15592994, 19780765, 24596948, 33821742, 33342683, 31285529; Phenotypes: Developmental and epileptic encephalopathy 3, MIM# 609304; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:42:40.207061+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12822","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A22 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:41:53.457529+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12821","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC25A22: Rating: GREEN; Mode of pathogenicity: None; Publications: 15592994, 19780765, 24596948, 33821742, 33342683, 31285529; Phenotypes: Developmental and epileptic encephalopathy 3, MIM# 609304; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A22","entity_type":"gene"},{"created":"2022-04-09T17:35:24.344312+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12821","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRPM1 as ready","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:35:24.309763+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12821","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trpm1 has been classified as Green List (High Evidence).","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:35:15.753512+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12821","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRPM1 were changed from  to Night blindness, congenital stationary (complete), 1C, autosomal recessive, MIM# 613216","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:34:54.739110+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12820","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRPM1 were set to ","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:34:35.837108+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12819","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRPM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:34:17.111627+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12818","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRPM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19878917, 19896113, 19896109; Phenotypes: Night blindness, congenital stationary (complete), 1C, autosomal recessive, MIM# 613216; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRPM1","entity_type":"gene"},{"created":"2022-04-09T17:32:49.565437+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.187","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRPC6 as ready","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:32:49.553738+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.187","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trpc6 has been classified as Green List (High Evidence).","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:32:47.347495+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.187","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRPC6 were changed from  to Glomerulosclerosis, focal segmental, 2, MIM# 603965","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:32:25.333226+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.186","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRPC6 were set to 15879175; 15924139; 34387384; 33918778; 32509715","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:32:04.070790+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.186","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRPC6 were set to ","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:31:49.882051+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12818","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRPC6 as ready","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:31:49.869401+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12818","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trpc6 has been classified as Green List (High Evidence).","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:31:26.464271+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.185","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRPC6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:30:54.406677+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.184","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRPC6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15879175, 15924139, 34387384, 33918778, 32509715; Phenotypes: Glomerulosclerosis, focal segmental, 2, MIM# 603965; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:30:52.262055+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12818","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRPC6 were changed from  to Glomerulosclerosis, focal segmental, 2, MIM# 603965","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:30:35.530841+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12817","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRPC6 were set to ","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:30:17.422521+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12816","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRPC6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:29:47.471759+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12815","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRPC6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15879175, 15924139, 34387384, 33918778, 32509715; Phenotypes: Glomerulosclerosis, focal segmental, 2, MIM# 603965; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRPC6","entity_type":"gene"},{"created":"2022-04-09T17:26:19.055615+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC2 as ready","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:26:19.039173+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc2 has been classified as Green List (High Evidence).","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:26:14.143200+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12815","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC2 as ready","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:26:14.127755+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12815","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc2 has been classified as Green List (High Evidence).","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:25:26.541263+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12815","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAPPC2 were changed from  to Spondyloepiphyseal dysplasia tarda, MIM# 313400","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:25:18.116836+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAPPC2 were changed from Spondyloepiphyseal dysplasia tarda 313400; Spondyloepiphyseal dysplasia tarda\t313400 to Spondyloepiphyseal dysplasia tarda, MIM# 313400","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:24:45.188639+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC2 were set to ","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:24:34.140181+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12814","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC2 were set to ","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:24:07.512153+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAPPC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10431248, 14755465, 33726005, 20301324, 32953644; Phenotypes: Spondyloepiphyseal dysplasia tarda, MIM# 313400; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:23:39.589887+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12813","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAPPC2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:23:03.129700+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAPPC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10431248, 14755465, 33726005, 20301324, 32953644; Phenotypes: Spondyloepiphyseal dysplasia tarda, MIM# 313400; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TRAPPC2","entity_type":"gene"},{"created":"2022-04-09T17:20:43.237689+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC12 as ready","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2022-04-09T17:20:43.227921+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2022-04-09T17:19:53.332353+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC11 as ready","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:19:53.318755+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc11 has been classified as Green List (High Evidence).","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:19:43.026018+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12812","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAPPC11 were changed from  to Muscular dystrophy, limb-girdle, autosomal recessive 18, MIM# 615356","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:19:17.958885+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12811","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC11 were set to ","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:18:57.442071+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12810","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAPPC11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:18:38.611968+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12809","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAPPC11: Rating: GREEN; Mode of pathogenicity: None; Publications: 23830518, 26322222, 29855340, 30105108; Phenotypes: Muscular dystrophy, limb-girdle, autosomal recessive 18, MIM# 615356; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAPPC11","entity_type":"gene"},{"created":"2022-04-09T17:17:35.308000+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAK1 as ready","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:17:35.297913+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trak1 has been classified as Green List (High Evidence).","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:17:12.531491+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAK1 were changed from  to Developmental and epileptic encephalopathy 68, MIM# 618201","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:17:07.138320+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12809","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAK1 as ready","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:17:07.126426+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12809","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trak1 has been classified as Green List (High Evidence).","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:16:47.443891+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12809","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAK1 were changed from  to Developmental and epileptic encephalopathy 68, MIM# 618201","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:16:27.969188+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1548","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAK1 were set to ","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:16:09.705836+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12808","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAK1 were set to ","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:15:52.917059+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1547","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:15:43.019399+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12807","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:15:09.360104+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12806","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28940097, 28364549, 29846532, 28924745; Phenotypes: Developmental and epileptic encephalopathy 68, MIM# 618201; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAK1","entity_type":"gene"},{"created":"2022-04-09T17:13:37.307383+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12806","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPMT as ready","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:13:37.297938+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12806","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpmt has been classified as Red List (Low Evidence).","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:13:28.054601+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12806","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TPMT were changed from  to {Thiopurines, poor metabolism of, 1} 610460","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:13:03.072409+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12805","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TPMT as Red List (low evidence)","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:13:03.057039+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12805","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpmt has been classified as Red List (Low Evidence).","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:12:43.375206+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12804","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TPMT: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Thiopurines, poor metabolism of, 1} 610460; Mode of inheritance: None","entity_name":"TPMT","entity_type":"gene"},{"created":"2022-04-09T17:11:03.833143+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12804","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRNT1 as ready","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:11:03.816631+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12804","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trnt1 has been classified as Green List (High Evidence).","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:10:54.673414+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12804","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRNT1 were changed from  to Retinitis pigmentosa and erythrocytic microcytosis, MIM# 616959; Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay, MIM# 616084","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:10:34.424710+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12803","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRNT1 were set to ","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:10:01.891599+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12802","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:09:41.656301+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12801","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25193871, 23553769, 29170023, 27389523, 26494905; Phenotypes: Retinitis pigmentosa and erythrocytic microcytosis, MIM# 616959, Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay, MIM# 616084; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRNT1","entity_type":"gene"},{"created":"2022-04-09T17:06:03.477665+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12801","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMU as ready","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:06:03.466277+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12801","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmu has been classified as Green List (High Evidence).","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:05:42.928165+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12801","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMU were changed from  to Liver failure, transient infantile, MIM# 613070","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:05:19.121898+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12800","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMU were set to ","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:04:44.625591+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12799","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:04:26.920484+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.787","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT5 as ready","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:04:26.908402+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.787","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt5 has been classified as Green List (High Evidence).","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:04:22.901955+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.787","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT5 were changed from  to Combined oxidative phosphorylation deficiency 26, MIM# 616539","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:03:46.444837+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.786","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT5 were set to ","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:03:00.348856+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12798","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRMU: Rating: GREEN; Mode of pathogenicity: None; Publications: 19732863; Phenotypes: Liver failure, transient infantile, MIM# 613070; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-04-09T17:02:19.253349+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.785","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMT5 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:01:11.985197+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.784","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMT5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:00:31.611690+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.783","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRMT5: Rating: GREEN; Mode of pathogenicity: None; Publications: 26189817, 35342985, 35109800, 29021354; Phenotypes: Combined oxidative phosphorylation deficiency 26, MIM# 616539; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:00:17.828634+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12798","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT5 as ready","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:00:17.801779+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt5 has been classified as Green List (High Evidence).","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T17:00:08.547156+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT5 were changed from  to Combined oxidative phosphorylation deficiency 26, MIM# 616539","entity_name":"TRMT5","entity_type":"gene"},{"created":"2022-04-09T16:59:41.854055+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12797","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT5 were set to ","entity_name":"TRMT5","entity_type":"gene"}]}