{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=667","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=665","results":[{"created":"2022-12-14T13:45:11.637344+11:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS15 as ready","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:45:11.623276+11:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15 has been classified as Red List (Low Evidence).","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:45:03.698989+11:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPS15 was added\ngene: RPS15 was added to Diamond Blackfan anaemia. Sources: Expert Review\nMode of inheritance for gene: RPS15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: RPS15 were set to 19061985\nPhenotypes for gene: RPS15 were set to Diamond-Blackfan anaemia, MONDO:0015253, RPS15-related\nReview for gene: RPS15 was set to RED\nAdded comment: Single individual reported in 2008, no reports since. \nSources: Expert Review","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:43:02.632706+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.554","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS15 as ready","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:43:02.616666+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.554","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15 has been classified as Red List (Low Evidence).","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:42:59.847227+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1401","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS15 were changed from Diamond-Blackfan anaemia to Diamond-Blackfan anaemia, MONDO:0015253, RPS15-related","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:42:33.637750+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.554","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS15 were changed from Diamond-Blackfan anaemia to Diamond-Blackfan anaemia, MONDO:0015253, RPS15-related","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:41:15.774219+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.553","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPS15 was added\ngene: RPS15 was added to Mendeliome. Sources: Expert Review\nMode of inheritance for gene: RPS15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: RPS15 were set to 19061985\nPhenotypes for gene: RPS15 were set to Diamond-Blackfan anaemia\nReview for gene: RPS15 was set to RED\nAdded comment: Single individual reported in 2008, no reports since. \nSources: Expert Review","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:40:58.313125+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1400","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS15 as ready","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:40:58.298476+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1400","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15 has been classified as Red List (Low Evidence).","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:40:45.219826+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1400","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS15 were changed from Diamond-Blackfan anemia to Diamond-Blackfan anaemia","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:40:30.439857+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1399","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS15 were set to ","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:39:21.072643+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1398","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS15 as Red List (low evidence)","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:39:21.060509+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1398","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15 has been classified as Red List (Low Evidence).","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:39:08.442011+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single individual reported.; to: Single individual reported in 2008, no reports since.","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:38:32.506532+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS15: Rating: RED; Mode of pathogenicity: None; Publications: 19061985; Phenotypes: Diamond-Blackfan anaemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS15","entity_type":"gene"},{"created":"2022-12-14T13:33:48.261880+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS15A as ready","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:33:48.250010+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15a has been classified as Red List (Low Evidence).","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:32:34.967811+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS15A as Red List (low evidence)","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:32:34.955398+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1397","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps15a has been classified as Red List (Low Evidence).","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:32:24.390065+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: RPS15A.\nTag treatable tag was added to gene: RPS15A.\nTag haematological tag was added to gene: RPS15A.","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:32:08.907939+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS15A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Diamond-Blackfan anaemia 20, MIM# 618313; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS15A","entity_type":"gene"},{"created":"2022-12-14T13:30:44.797732+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS17 as ready","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-12-14T13:30:44.785874+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps17 has been classified as Green List (High Evidence).","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-12-14T13:30:37.880866+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: RPS17.\nTag haematological tag was added to gene: RPS17.","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-12-14T13:30:20.347633+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPS17: Changed phenotypes: Diamond-Blackfan anaemia 4, MIM# 612527","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-12-14T13:29:57.914521+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS17","entity_type":"gene"},{"created":"2022-12-14T13:28:31.594235+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS19 as ready","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-12-14T13:28:31.581847+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps19 has been classified as Green List (High Evidence).","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-12-14T13:28:24.589313+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: RPS19.\nTag haematological tag was added to gene: RPS19.","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-12-14T13:28:10.818621+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPS19: Changed phenotypes: Diamond-Blackfan anaemia 1, MIM# 105650","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-12-14T13:27:53.587030+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS19: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS19","entity_type":"gene"},{"created":"2022-12-14T13:26:48.068327+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS24 as ready","entity_name":"RPS24","entity_type":"gene"},{"created":"2022-12-14T13:26:48.045004+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps24 has been classified as Green List (High Evidence).","entity_name":"RPS24","entity_type":"gene"},{"created":"2022-12-14T13:26:42.083705+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: RPS24.\nTag haematological tag was added to gene: RPS24.","entity_name":"RPS24","entity_type":"gene"},{"created":"2022-12-14T13:26:27.848131+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPS24: Changed phenotypes: Diamond-blackfan anaemia 3, MIM# 610629","entity_name":"RPS24","entity_type":"gene"},{"created":"2022-12-14T13:26:12.280787+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS24: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS24","entity_type":"gene"},{"created":"2022-12-14T13:25:15.702613+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS26 as ready","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-12-14T13:25:15.688825+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps26 has been classified as Green List (High Evidence).","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-12-14T13:25:10.173318+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: RPS26.\nTag haematological tag was added to gene: RPS26.","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-12-14T13:24:51.989884+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS26: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Diamond-Blackfan anaemia 10, MIM# 613309; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS26","entity_type":"gene"},{"created":"2022-12-14T12:39:38.760493+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: SMARCAL1 as ready","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:39:38.748480+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Seb Lunke","item_type":"entity","text":"Gene: smarcal1 has been classified as Amber List (Moderate Evidence).","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:39:33.888798+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1396","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: SMARCAL1 were changed from Schimke immunoosseous dysplasia to Schimke immune-osseous dysplasia MIM# 242900","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:39:11.118177+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1395","user_name":"Seb Lunke","item_type":"entity","text":"Classified gene: SMARCAL1 as Amber List (moderate evidence)","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:39:11.106881+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1395","user_name":"Seb Lunke","item_type":"entity","text":"Gene: smarcal1 has been classified as Amber List (Moderate Evidence).","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:39:00.821941+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1394","user_name":"Seb Lunke","item_type":"entity","text":"Tag for review tag was added to gene: SMARCAL1.","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:38:48.672779+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1394","user_name":"Seb Lunke","item_type":"entity","text":"reviewed gene: SMARCAL1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Schimke immune-osseous dysplasia MIM# 242900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2022-12-14T12:31:28.209238+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1394","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: SMAD4 as ready","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:31:28.175456+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1394","user_name":"Seb Lunke","item_type":"entity","text":"Gene: smad4 has been classified as Red List (Low Evidence).","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:31:20.939330+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1394","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: SMAD4 were changed from Juvenile polyposis syndrome to Polyposis, juvenile intestinal, MIM# 174900; Myhre syndrome, MIM# 139210","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:31:07.945174+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1393","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: SMAD4 were set to ","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:30:58.235296+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1392","user_name":"Seb Lunke","item_type":"entity","text":"Classified gene: SMAD4 as Red List (low evidence)","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:30:58.217189+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1392","user_name":"Seb Lunke","item_type":"entity","text":"Gene: smad4 has been classified as Red List (Low Evidence).","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:29:31.270796+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1391","user_name":"Seb Lunke","item_type":"entity","text":"reviewed gene: SMAD4: Rating: RED; Mode of pathogenicity: None; Publications: 20301642; Phenotypes: Polyposis, juvenile intestinal, MIM# 174900, Myhre syndrome, MIM# 139210; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMAD4","entity_type":"gene"},{"created":"2022-12-14T12:15:05.281491+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1391","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: SMAD3 as ready","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T12:15:05.268997+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1391","user_name":"Seb Lunke","item_type":"entity","text":"Gene: smad3 has been classified as Green List (High Evidence).","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T12:14:46.638577+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1391","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: SMAD3 were changed from Loeys-Dietz syndrome to Loeys-Dietz syndrome 3, MIM# 613795","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T12:14:33.560717+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1390","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: SMAD3 were set to ","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T12:14:19.965931+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Seb Lunke","item_type":"entity","text":"Tag for review tag was added to gene: SMAD3.","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T12:14:05.814503+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Seb Lunke","item_type":"entity","text":"reviewed gene: SMAD3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301312; Phenotypes: Loeys-Dietz syndrome 3, MIM# 613795; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMAD3","entity_type":"gene"},{"created":"2022-12-14T10:01:48.782823+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC4A1.\nTag renal tag was added to gene: SLC4A1.","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2022-12-14T09:54:45.212853+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC52A2.\nTag metabolic tag was added to gene: SLC52A2.","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2022-12-14T09:54:17.078004+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC52A3.\nTag metabolic tag was added to gene: SLC52A3.","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2022-12-14T09:53:41.945971+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC5A1.\nTag gastrointestinal tag was added to gene: SLC5A1.","entity_name":"SLC5A1","entity_type":"gene"},{"created":"2022-12-14T09:53:03.922119+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC5A5.\nTag endocrine tag was added to gene: SLC5A5.","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-12-14T09:52:50.258117+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC5A5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC5A5","entity_type":"gene"},{"created":"2022-12-14T09:51:03.454312+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC6A8 as ready","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:51:03.441661+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a8 has been classified as Amber List (Moderate Evidence).","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:50:59.150003+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1389","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC6A8 were set to ","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:50:49.267636+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1388","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC6A8 as Amber List (moderate evidence)","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:50:49.256111+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1388","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a8 has been classified as Amber List (Moderate Evidence).","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:50:37.954449+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1387","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: SLC6A8.\nTag metabolic tag was added to gene: SLC6A8.","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:50:24.610328+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1387","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC6A8: Rating: AMBER; Mode of pathogenicity: None; Publications: 24953403; Phenotypes: Cerebral creatine deficiency syndrome 1, MIM# 300352; Mode of inheritance: None","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2022-12-14T09:47:40.553397+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1387","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLC7A7.\nTag metabolic tag was added to gene: SLC7A7.","entity_name":"SLC7A7","entity_type":"gene"},{"created":"2022-12-14T09:46:57.888266+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1387","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC7A9 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC7A9","entity_type":"gene"},{"created":"2022-12-14T09:46:45.537214+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: SLC7A9.","entity_name":"SLC7A9","entity_type":"gene"},{"created":"2022-12-14T09:46:35.398913+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC7A9: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cystinuria, MIM# 220100; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC7A9","entity_type":"gene"},{"created":"2022-12-14T09:43:26.403005+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: SLX4.\nTag haematological tag was added to gene: SLX4.","entity_name":"SLX4","entity_type":"gene"},{"created":"2022-12-14T09:41:56.951055+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS27 as ready","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:41:56.938733+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps27 has been classified as Red List (Low Evidence).","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:41:51.416529+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS27 as Red List (low evidence)","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:41:51.404388+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps27 has been classified as Red List (Low Evidence).","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:41:41.972227+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: RPS27.\nTag treatable tag was added to gene: RPS27.\nTag haematological tag was added to gene: RPS27.","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:41:26.460905+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS27: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Diamond-Blackfan anemia 17, MIM# 617409; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS27","entity_type":"gene"},{"created":"2022-12-14T09:40:11.504945+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:40:11.491078+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Red List (Low Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:40:06.710638+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Red List (low evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:40:06.697691+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1385","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Red List (Low Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:39:56.787813+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: RPS28.\nTag treatable tag was added to gene: RPS28.\nTag haematological tag was added to gene: RPS28.","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:39:41.926239+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Congenital onset.\r\n\r\nDBA is a treatable disorder: corticosteroids, red blood cell transfusion, BMT.; to: Two individuals reported in 2014, none since.\r\n\r\nCongenital onset.\r\n\r\nDBA is a treatable disorder: corticosteroids, red blood cell transfusion, BMT.","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:39:26.686021+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPS28: Changed rating: RED; Changed phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:38:57.120422+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: RPS28","entity_name":"RPS28","entity_type":"gene"},{"created":"2022-12-14T09:38:26.908008+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS29 as ready","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:38:26.888169+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Red List (Low Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:38:21.439254+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS29 as Red List (low evidence)","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:38:21.425529+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1384","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Red List (Low Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:37:30.985844+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1383","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: RPS29.\nTag treatable tag was added to gene: RPS29.\nTag haematological tag was added to gene: RPS29.","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:37:14.755556+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1383","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS29: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Diamond-Blackfan anemia 13, MIM# 615909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2022-12-14T09:35:38.798833+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1383","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS6KA3 as ready","entity_name":"RPS6KA3","entity_type":"gene"}]}