{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1119","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1117","results":[{"created":"2021-11-24T23:03:13.323635+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.61","user_name":"Lavvina Thiyagarajan","item_type":"entity","text":"gene: TNFAIP3 was added\ngene: TNFAIP3 was added to Inflammatory bowel disease. Sources: Literature\nMode of inheritance for gene: TNFAIP3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TNFAIP3 were set to 34030699, 33446651, 32521965, 31299923\nPhenotypes for gene: TNFAIP3 were set to Inflammatory bowel disease; Crohn's disease; Autoinflammatory syndrome, familial, Behcet-like\nPenetrance for gene: TNFAIP3 were set to unknown\nReview for gene: TNFAIP3 was set to GREEN\nAdded comment: 4 unrelated individuals with inflammatory bowel disease and variants TNFAIP3 - haploinsufficiency suggested as disease mechanism. \nSources: Literature","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-24T18:51:30.995152+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9856","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA4 as ready","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:51:30.985397+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9856","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba4 has been classified as Green List (High Evidence).","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:51:21.061307+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9856","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA4 were changed from  to Cataract 23, MIM# 610425","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:51:00.920305+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9855","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA4 were set to ","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:50:39.663993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9854","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:50:20.704179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9853","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA4: Rating: GREEN; Mode of pathogenicity: None; Publications: 16960806, 16960806, 20577656; Phenotypes: Cataract 23, MIM# 610425; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:49:41.357791+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA4 as ready","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:49:41.345232+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba4 has been classified as Green List (High Evidence).","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:49:31.842282+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA4 were changed from  to Cataract 23, MIM# 610425","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:49:04.731149+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA4 were set to ","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:48:21.909172+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.302","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:47:55.694957+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA4: Rating: GREEN; Mode of pathogenicity: None; Publications: 16960806, 16960806, 20577656; Phenotypes: Cataract 23, MIM# 610425; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:47:14.714942+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA4 as ready","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:47:14.703019+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba4 has been classified as Green List (High Evidence).","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:47:11.230188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA4 were changed from CATARACT ZONULAR TYPE 2 to Cataract 23, MIM# 610425","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:46:56.660400+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.700","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA4 were set to ","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:46:38.244628+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.699","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:46:23.684174+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA4: Rating: GREEN; Mode of pathogenicity: None; Publications: 16960806, 16960806, 20577656; Phenotypes: Cataract 23, MIM# 610425; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA4","entity_type":"gene"},{"created":"2021-11-24T18:32:30.331548+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA1 as ready","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:32:30.321226+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba1 has been classified as Green List (High Evidence).","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:32:27.954091+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA1 were changed from  to Cataract 10, multiple types, MIM# 600881","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:31:51.878801+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA1 were set to ","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:31:28.219211+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:31:03.430851+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9788845, 14598164, 34419537, 33827296, 31488069; Phenotypes: Cataract 10, multiple types, MIM# 600881; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:30:25.527109+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9853","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA1 as ready","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:30:25.511835+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9853","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba1 has been classified as Green List (High Evidence).","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:28:33.412730+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9853","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA1 were changed from  to Cataract 10, multiple types, MIM# 600881","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:28:12.764429+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9852","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA1 were set to ","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:27:56.035652+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9851","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:27:53.710880+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9851","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:27:32.633146+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9850","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9788845, 14598164, 34419537, 33827296, 31488069; Phenotypes: Cataract 10, multiple types, MIM# 600881; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:26:46.661318+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBA1 as ready","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:26:46.652520+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryba1 has been classified as Green List (High Evidence).","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:26:42.761698+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBA1 were changed from CATARACT CONGENITAL ZONULAR WITH SUTURAL OPACITIES to Cataract 10, multiple types, MIM# 600881","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:26:27.332201+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.697","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBA1 were set to ","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:26:09.415531+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.696","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBA1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:25:56.030221+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.695","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9788845, 14598164, 34419537, 33827296, 31488069; Phenotypes: Cataract 10, multiple types, MIM# 600881; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBA1","entity_type":"gene"},{"created":"2021-11-24T18:23:45.262776+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYAA as ready","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:23:45.252936+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryaa has been classified as Green List (High Evidence).","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:22:55.462031+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYAA were changed from  to Cataract 9, multiple types, MIM# 604219","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:22:26.946597+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYAA were set to ","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:22:03.053952+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.296","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYAA was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:21:32.138588+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.295","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYAA: Rating: GREEN; Mode of pathogenicity: None; Publications: 9467006, 11006246, 16735993, 17724170, 23255486; Phenotypes: Cataract 9, multiple types, MIM# 604219; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:20:53.012263+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9850","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYAA as ready","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:20:53.001223+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9850","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryaa has been classified as Green List (High Evidence).","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:20:42.436716+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9850","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYAA were changed from  to Cataract 9, multiple types, MIM# 604219","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:19:21.608422+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9849","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYAA were set to ","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:18:58.951259+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9848","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYAA was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:18:39.077128+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9847","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYAA: Rating: GREEN; Mode of pathogenicity: None; Publications: 9467006, 11006246, 16735993, 17724170, 23255486; Phenotypes: Cataract 9, multiple types, MIM# 604219; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:17:42.578822+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.695","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYAA as ready","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:17:42.568109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.695","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryaa has been classified as Green List (High Evidence).","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:17:38.765018+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.695","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYAA were changed from CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 1; CATARACT, NUCLEAR to Cataract 9, multiple types, MIM# 604219","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:17:12.247597+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.694","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYAA were set to ","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:16:55.704057+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.693","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYAA: Rating: GREEN; Mode of pathogenicity: None; Publications: 9467006, 11006246, 16735993, 17724170, 23255486; Phenotypes: Cataract 9, multiple types, MIM# 604219; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYAA","entity_type":"gene"},{"created":"2021-11-24T18:14:28.783369+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.693","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRTAP as ready","entity_name":"CRTAP","entity_type":"gene"},{"created":"2021-11-24T18:14:28.773544+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.693","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crtap has been classified as Green List (High Evidence).","entity_name":"CRTAP","entity_type":"gene"},{"created":"2021-11-24T18:14:24.843651+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.693","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRTAP were changed from Osteogenesis imperfecta, type VII 610682 to Osteogenesis imperfecta, type VII, MIM# 610682","entity_name":"CRTAP","entity_type":"gene"},{"created":"2021-11-24T18:14:13.832464+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.692","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRTAP were set to ","entity_name":"CRTAP","entity_type":"gene"},{"created":"2021-11-24T18:12:43.368086+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DICER1 as ready","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T18:12:43.355512+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dicer1 has been classified as Green List (High Evidence).","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T18:12:40.158874+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DICER1 were changed from GLOW syndrome, somatic mosaic - OMIM#618272; Goiter, multinodular 1, with or without Sertoli-Leydig cell tumors - OMIM#38800; Pleuropulmonary blastoma - OMIM#601200; Rhabdomyosarcoma, embryonal, 2 - #180295 to DICER1 syndrome, MONDO:0017288","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T18:10:12.438470+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DICER1 as Green List (high evidence)","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T18:10:12.428369+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dicer1 has been classified as Green List (High Evidence).","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T18:09:24.020788+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9847","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CALU as ready","entity_name":"CALU","entity_type":"gene"},{"created":"2021-11-24T18:09:24.009655+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9847","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: calu has been classified as Red List (Low Evidence).","entity_name":"CALU","entity_type":"gene"},{"created":"2021-11-24T18:09:15.796050+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9847","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CALU as Red List (low evidence)","entity_name":"CALU","entity_type":"gene"},{"created":"2021-11-24T18:09:15.784307+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9847","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: calu has been classified as Red List (Low Evidence).","entity_name":"CALU","entity_type":"gene"},{"created":"2021-11-24T14:59:45.508571+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.691","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2AK3 as ready","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-24T14:59:45.495483+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.691","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2ak3 has been classified as Green List (High Evidence).","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-24T14:59:41.836945+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.691","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2AK3 were changed from WOLCOTT-RALLISON SYNDROME to Wolcott-Rallison syndrome MIM#226980","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-24T14:44:38.419433+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.93","user_name":"Krithika Murali","item_type":"entity","text":"gene: DICER1 was added\ngene: DICER1 was added to Macrocephaly_Megalencephaly. Sources: Literature\nMode of inheritance for gene: DICER1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DICER1 were set to 27441995\nPhenotypes for gene: DICER1 were set to GLOW syndrome, somatic mosaic - OMIM#618272; Goiter, multinodular 1, with or without Sertoli-Leydig cell tumors - OMIM#38800; Pleuropulmonary blastoma - OMIM#601200; Rhabdomyosarcoma, embryonal, 2 - #180295\nReview for gene: DICER1 was set to GREEN\nAdded comment: PMID 27441995 - 28 DICER1 carriers were macrocephalic (42% of the NCI natural history cohort) versus 12% family controls [statistically significant].  Association independent of height and gender.  The authors note this is a subtle but important phenotypic feature which would allow for initiation of cancer surveillance earlier, as with PTEN carriers. \nSources: Literature","entity_name":"DICER1","entity_type":"gene"},{"created":"2021-11-24T14:30:44.672512+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.690","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2AK3 were set to ","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-24T14:30:30.924581+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2AK3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-24T10:03:38.414379+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9846","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CALU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes","entity_name":"CALU","entity_type":"gene"},{"created":"2021-11-23T18:40:14.536001+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.689","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: EIF2AK3: Rating: AMBER; Mode of pathogenicity: None; Publications: 10932183, 7551159, 16813601; Phenotypes: Wolcott-Rallison syndrome MIM#226980; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2021-11-23T18:33:38.434130+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9846","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDNRA as ready","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:33:38.422896+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9846","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ednra has been classified as Green List (High Evidence).","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:33:31.070957+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9846","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EDNRA were changed from  to Mandibulofacial dysostosis with alopecia, MIM# 616367","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:33:10.504476+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9845","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EDNRA were set to ","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:32:52.431303+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9844","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EDNRA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:32:35.485191+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9843","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EDNRA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25772936, 27671791; Phenotypes: Mandibulofacial dysostosis with alopecia, MIM# 616367; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:31:38.587721+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDNRA as ready","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:31:38.572225+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ednra has been classified as Green List (High Evidence).","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:31:34.667964+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EDNRA were changed from MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA to Mandibulofacial dysostosis with alopecia, MIM# 616367","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:31:22.064133+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.688","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EDNRA were set to ","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T18:30:51.482593+11:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNPO3 as ready","entity_name":"TNPO3","entity_type":"gene"},{"created":"2021-11-23T18:30:51.472972+11:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnpo3 has been classified as Green List (High Evidence).","entity_name":"TNPO3","entity_type":"gene"},{"created":"2021-11-23T18:30:48.101237+11:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNPO3 were set to ","entity_name":"TNPO3","entity_type":"gene"},{"created":"2021-11-23T18:30:34.014471+11:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: TNPO3 was changed from  to Other","entity_name":"TNPO3","entity_type":"gene"},{"created":"2021-11-23T18:29:57.442889+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.687","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDA as ready","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:57.432666+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.687","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eda has been classified as Red List (Low Evidence).","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:53.872391+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.687","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EDA were changed from ECTODERMAL DYSPLASIA TYPE 1; TOOTH AGENESIS SELECTIVE X-LINKED TYPE 1 to Ectodermal dysplasia 1, hypohidrotic, X-linked, MIM# 305100; MONDO:0010585","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:41.665701+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.686","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EDA were set to ","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:14.731790+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.685","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EDA as Red List (low evidence)","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:14.722052+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.685","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eda has been classified as Red List (Low Evidence).","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T18:29:02.984836+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EDA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"EDA","entity_type":"gene"},{"created":"2021-11-23T14:16:39.791231+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: EDNRA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25772936, 27671791; Phenotypes: Mandibulofacial dysostosis with alopecia, MIM# 616367; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"EDNRA","entity_type":"gene"},{"created":"2021-11-23T11:13:37.481699+11:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.59","user_name":"Teresa Zhao","item_type":"entity","text":"reviewed gene: TNPO3: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 23667635, 23543484, 31071488, 31192305; Phenotypes: Limb-girdle muscular dystrophy 2 (MIM#608423; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"TNPO3","entity_type":"gene"},{"created":"2021-11-23T10:43:53.289506+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: EDA: Rating: AMBER; Mode of pathogenicity: None; Publications: 29694819, 19921643, 18510547, 9507389; Phenotypes: Ectodermal dysplasia 1, hypohidrotic, X-linked, MIM# 305100, MONDO:0010585; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes","entity_name":"EDA","entity_type":"gene"}]}