{"count":220265,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1368","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1366","results":[{"created":"2021-03-28T20:13:59.477297+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3569","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARP7 were changed from  to Alazami syndrome, MIM# 615071; Microcephalic primordial dwarfism, Alazami type MONDO:0014031","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:13:39.046732+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3568","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARP7 were set to ","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:13:06.845284+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3567","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:12:39.315703+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3566","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:11:15.144043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6953","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARP7 as ready","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:11:15.133179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6953","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: larp7 has been classified as Green List (High Evidence).","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:10:54.394597+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6953","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARP7 were changed from  to Alazami syndrome, MIM# 615071; Microcephalic primordial dwarfism, Alazami type MONDO:0014031","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:10:19.194093+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARP7 as ready","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:10:19.183234+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: larp7 has been classified as Green List (High Evidence).","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:10:12.176884+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6952","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARP7 were set to ","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:10:10.672517+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARP7 were changed from  to Alazami syndrome, MIM# 615071; Microcephalic primordial dwarfism, Alazami type MONDO:0014031","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:09:27.830377+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6951","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:09:15.158174+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARP7 were set to ","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:09:03.020356+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6950","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:08:41.280316+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARP7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:08:26.978110+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T20:07:52.147590+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARP7","entity_type":"gene"},{"created":"2021-03-28T19:58:23.808274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3566","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KNL1 as ready","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:58:23.798607+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3566","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: knl1 has been classified as Green List (High Evidence).","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:58:19.923608+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3566","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KNL1 were changed from  to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:57:53.620084+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3565","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KNL1 were set to ","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:57:28.341033+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:57:00.640904+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:56:51.272086+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KNL1 as ready","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:56:51.261367+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: knl1 has been classified as Green List (High Evidence).","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:56:16.660662+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6950","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KNL1 as ready","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:56:16.648680+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6950","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: knl1 has been classified as Green List (High Evidence).","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:56:08.864623+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6950","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KNL1 were changed from  to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:55:51.088962+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6949","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KNL1 were set to ","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:55:31.255081+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6948","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:55:20.072924+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.562","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KNL1 were changed from  to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:55:07.680163+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6947","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:54:32.799024+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.561","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KNL1 were set to ","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:54:09.053232+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.560","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:53:45.072035+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KNL1: Changed phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:53:24.203738+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KNL1","entity_type":"gene"},{"created":"2021-03-28T19:48:31.052027+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:48:05.734489+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TNRC6B: Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:47:55.322747+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6947","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:47:35.454395+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6946","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TNRC6B: Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:47:32.425290+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:46:48.980277+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3562","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TNRC6B: Changed rating: GREEN; Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNRC6B","entity_type":"gene"},{"created":"2021-03-28T19:45:19.531854+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6946","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BAAT as ready","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:45:19.522322+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6946","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: baat has been classified as Green List (High Evidence).","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:45:12.532552+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6946","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BAAT were changed from  to Bile acid conjugation defect 1, MIM# 619232","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:44:53.711599+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6945","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BAAT were set to ","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:44:33.348244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6944","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BAAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:44:15.745868+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6943","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: 12704386, 23415802; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:44:07.167882+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.191","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BAAT were changed from  to Bile acid conjugation defect 1, MIM# 619232","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:43:43.386411+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BAAT were set to ","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:38:16.198382+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.189","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BAAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:37:46.443347+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.188","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: 12704386, 23415802; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:36:54.995058+11:00","panel_name":"Miscellaneous Metabolic Disorders","panel_id":3468,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BAAT were changed from Hypercholanemia, familial MIM#607748; disorder of bile acid metabolism to Bile acid conjugation defect 1, MIM# 619232; Hypercholanemia, familial MIM#607748; disorder of bile acid metabolism","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T19:36:14.246513+11:00","panel_name":"Miscellaneous Metabolic Disorders","panel_id":3468,"panel_version":"1.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BAAT","entity_type":"gene"},{"created":"2021-03-28T18:07:31.812091+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:07:31.798882+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Green List (High Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:07:29.929938+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MIM#152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:07:18.353314+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to ","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:07:06.616925+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:06:26.650729+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3562","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:06:03.085427+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation MIM#152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:04:51.642382+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3560","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to 24281367","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:04:01.768682+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:03:49.743377+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:03:49.734240+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Green List (High Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:03:11.941713+11:00","panel_name":"Lymphoedema_syndromic","panel_id":3098,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:03:11.931807+11:00","panel_name":"Lymphoedema_syndromic","panel_id":3098,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Green List (High Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:03:09.363913+11:00","panel_name":"Lymphoedema_syndromic","panel_id":3098,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MCLMR 152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:02:58.851967+11:00","panel_name":"Lymphoedema_syndromic","panel_id":3098,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to 22284827","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T18:02:45.128825+11:00","panel_name":"Lymphoedema_syndromic","panel_id":3098,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:59:47.304089+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from  to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:58:10.204771+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:58:10.193939+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Red List (Low Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:58:07.268488+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from  to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:57:38.469527+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.267","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:57:16.635696+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.266","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF11 as Red List (low evidence)","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:57:16.622311+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.266","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Red List (Low Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:56:47.032161+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:55:37.485405+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6943","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:55:37.475431+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6943","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Green List (High Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:55:30.818570+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6943","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from  to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:55:14.009717+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6942","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to ","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:54:56.638575+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6941","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:54:40.159068+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6940","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:54:31.497275+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.558","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to ","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:53:51.555181+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.557","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:53:48.272278+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IER3IP1 as ready","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:53:48.261956+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ier3ip1 has been classified as Green List (High Evidence).","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:53:46.040122+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IER3IP1 were changed from Microcephaly, epilepsy, and diabetes syndrome to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:53:20.120577+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.556","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-03-28T17:48:08.181033+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IER3IP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21835305, 22991235, 24138066, 28711742; Phenotypes: Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231, Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:47:34.995219+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IER3IP1 as ready","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:47:34.985125+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ier3ip1 has been classified as Green List (High Evidence).","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:47:30.833018+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IER3IP1 were changed from  to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:47:03.960992+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3558","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IER3IP1 were set to ","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:46:42.951282+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3557","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IER3IP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:46:09.307252+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3556","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IER3IP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21835305, 22991235, 24138066, 28711742; Phenotypes: Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231, Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:45:39.886149+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IER3IP1 as ready","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:45:39.875578+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ier3ip1 has been classified as Green List (High Evidence).","entity_name":"IER3IP1","entity_type":"gene"},{"created":"2021-03-28T17:45:37.083684+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IER3IP1 were changed from  to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647","entity_name":"IER3IP1","entity_type":"gene"}]}