{"count":220488,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1533","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1531","results":[{"created":"2020-10-18T20:53:20.642248+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI2 as ready","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:53:20.634489+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai2 has been classified as Green List (High Evidence).","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:53:13.324690+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GAS8 as ready","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:53:13.314718+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gas8 has been classified as Green List (High Evidence).","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:53:10.031853+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GAS8 were changed from  to Ciliary dyskinesia, primary, 33, mIM# 616726","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:52:46.692724+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GAS8 were set to ","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:52:19.827720+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GAS8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:51:51.944659+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GAS8: Rating: GREEN; Mode of pathogenicity: None; Publications: 26387594, 27120127; Phenotypes: Ciliary dyskinesia, primary, 33, mIM# 616726; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GAS8","entity_type":"gene"},{"created":"2020-10-18T20:46:33.129709+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI2 were changed from  to Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:59.640633+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI2 were set to ","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:58.585753+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5023","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI2 as ready","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:58.571020+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5023","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai2 has been classified as Green List (High Evidence).","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:51.009367+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5023","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI2 were changed from  to Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:35.918204+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:45:24.268764+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5022","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI2 were set to ","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:44:54.267048+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:44:44.928300+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5021","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:44:12.070494+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI2 were changed from  to Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:44:05.427472+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5020","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18950741, 23261302; Phenotypes: Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:44:00.705036+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18950741, 23261302; Phenotypes: Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:43:47.063529+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI2 were set to ","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:42:49.766483+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:42:21.947372+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three unrelated families reported.; to: Four unrelated families reported.","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:42:05.347753+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18950741, 23261302; Phenotypes: Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI2","entity_type":"gene"},{"created":"2020-10-18T20:39:22.725899+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5020","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI1 as ready","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:39:22.715375+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5020","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai1 has been classified as Green List (High Evidence).","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:39:13.476262+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5020","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI1 were changed from  to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:38:55.472917+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5019","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI1 were set to ","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:38:37.102117+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5018","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:38:18.031478+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5017","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10577904, 11231901, 32502479, 31765523, 30622330; Phenotypes: Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:37:50.100453+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI1 as ready","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:37:50.092385+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai1 has been classified as Green List (High Evidence).","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:37:29.310927+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI1 were changed from  to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:37:06.882851+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI1 were set to ","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:36:40.052201+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:36:12.060835+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10577904, 11231901, 32502479, 31765523, 30622330; Phenotypes: Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:35:30.837063+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI1 as ready","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:35:30.822487+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai1 has been classified as Green List (High Evidence).","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:35:28.142825+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI1 were changed from  to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:35:00.942807+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI1 were set to ","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:34:33.423783+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:34:05.084701+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10577904, 11231901, 32502479, 31765523, 30622330; Phenotypes: Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-10-18T20:30:42.845693+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5017","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH11 were set to ","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:30:24.160796+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5016","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAH11: Rating: GREEN; Mode of pathogenicity: None; Publications: 12142464, 18022865, 22102620, 32633470, 31879361, 31765523, 31040315; Phenotypes: Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:47.929478+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH11 as ready","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:47.919220+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah11 has been classified as Green List (High Evidence).","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:44.039362+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH11 were changed from  to Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:16.639806+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH11 were set to ","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:15.366145+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH11 as ready","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:29:15.351619+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah11 has been classified as Green List (High Evidence).","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:28:57.579627+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH11 were changed from  to Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:28:51.524213+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAH11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:28:19.086969+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAH11: Rating: GREEN; Mode of pathogenicity: None; Publications: 12142464, 18022865, 22102620, 32633470, 31879361, 31765523, 31040315; Phenotypes: Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:28:12.541592+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH11 were set to ","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:27:34.265650+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAH11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:27:06.407294+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAH11: Rating: GREEN; Mode of pathogenicity: None; Publications: 12142464, 18022865, 22102620, 32633470, 31879361, 31765523, 31040315; Phenotypes: Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-10-18T20:23:57.519751+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5016","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF5 as ready","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:23:57.511534+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5016","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf5 has been classified as Green List (High Evidence).","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:23:50.604855+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5016","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF5 were changed from  to Ciliary dyskinesia, primary, 18, MIM# 614874","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:23:31.248223+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5015","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF5 were set to ","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:23:01.163656+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5014","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:22:41.881746+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5013","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23040496, 29363216, 25232951; Phenotypes: Ciliary dyskinesia, primary, 18, MIM# 614874; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:21:55.622158+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF5 as ready","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:21:55.601855+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf5 has been classified as Green List (High Evidence).","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:21:52.337577+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF5 were changed from  to Ciliary dyskinesia, primary, 18, MIM# 614874","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:21:16.377516+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF5 were set to ","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:20:48.729477+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:20:20.706887+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23040496, 29363216, 25232951; Phenotypes: Ciliary dyskinesia, primary, 18, MIM# 614874; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:18:58.678220+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF5 as ready","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:18:58.667500+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf5 has been classified as Green List (High Evidence).","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:18:55.947214+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF5 were changed from  to Ciliary dyskinesia, primary, 18, MIM# 614874","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:18:29.203443+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF5 were set to ","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:18:02.347290+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T20:17:33.063565+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23040496, 29363216, 25232951; Phenotypes: Ciliary dyskinesia, primary, 18, MIM# 614874; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF5","entity_type":"gene"},{"created":"2020-10-18T19:11:13.540002+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5013","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF3 as ready","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:11:13.529174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5013","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf3 has been classified as Green List (High Evidence).","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:11:07.119931+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5013","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF3 were changed from  to Ciliary dyskinesia, primary, 2, MIM# 606763","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:10:48.233118+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5012","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF3 were set to ","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:10:29.474244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5011","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:10:10.665596+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5010","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 22387996, 32622824, 31186518; Phenotypes: Ciliary dyskinesia, primary, 2, MIM# 606763; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:09:21.777864+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF3 as ready","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:09:21.770365+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf3 has been classified as Green List (High Evidence).","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:09:19.427937+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF3 were changed from  to Ciliary dyskinesia, primary, 2, MIM# 606763","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:08:49.267714+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF3 were set to ","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:08:21.289620+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:07:52.095956+11:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 22387996, 32622824, 31186518; Phenotypes: Ciliary dyskinesia, primary, 2, MIM# 606763; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:07:23.112605+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAAF3 as ready","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:07:23.104516+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnaaf3 has been classified as Green List (High Evidence).","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:07:01.364832+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAAF3 were changed from  to Ciliary dyskinesia, primary, 2, MIM# 606763","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:06:32.181324+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAAF3 were set to ","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:06:04.273597+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T19:05:35.555768+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAAF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 22387996, 32622824, 31186518; Phenotypes: Ciliary dyskinesia, primary, 2, MIM# 606763; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAAF3","entity_type":"gene"},{"created":"2020-10-18T17:36:53.405207+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB27A as ready","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:36:53.395196+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab27a has been classified as Green List (High Evidence).","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:36:50.785271+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB27A were changed from  to Griscelli syndrome, type 2, MIM# 607624","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:36:22.814432+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB27A were set to ","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:35:54.248791+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB27A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:35:24.371072+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB27A: Rating: GREEN; Mode of pathogenicity: None; Publications: 10835631, 10704277, 19030707, 15163896, 12058346, 10859366; Phenotypes: Griscelli syndrome, type 2, MIM# 607624; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:34:57.592153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5010","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB27A as ready","entity_name":"RAB27A","entity_type":"gene"},{"created":"2020-10-18T17:34:57.583971+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5010","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab27a has been classified as Green List (High Evidence).","entity_name":"RAB27A","entity_type":"gene"}]}