{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1118","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1116","results":[{"created":"2021-11-25T18:09:14.824310+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.314","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:08:49.718455+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:08:11.962086+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9877","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGC as ready","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:08:11.953390+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9877","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygc has been classified as Green List (High Evidence).","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:08:04.104894+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9877","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGC were changed from  to Cataract 2, multiple types, MIM# 604307","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:07:42.777138+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9876","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGC were set to ","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:07:19.210720+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9875","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:07:01.962808+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9874","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:06:06.853987+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGC as ready","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:06:06.844348+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygc has been classified as Green List (High Evidence).","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:06:02.412595+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGC were changed from CATARACT AUTOSOMAL DOMINANT to Cataract 2, multiple types, MIM# 604307","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:05:48.815717+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.711","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGC were set to ","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:05:34.383433+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.710","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGC was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:05:21.498976+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.709","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:02:28.727603+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB3 as ready","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:02:28.718772+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb3 has been classified as Green List (High Evidence).","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:02:25.876223+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB3 were changed from  to Cataract 22, MIM# 609741","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:01:55.815663+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB3 were set to ","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:01:25.346691+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.311","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:00:57.648163+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:00:15.828168+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9874","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB3 as ready","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:00:15.793144+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9874","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb3 has been classified as Green List (High Evidence).","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T18:00:02.378631+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9874","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB3 were changed from  to Cataract 22, MIM# 609741","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:59:40.808412+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9873","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB3 were set to ","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:56:02.499114+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9872","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:55:42.982690+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9871","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:54:56.024846+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.709","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB3 as ready","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:54:56.015327+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.709","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb3 has been classified as Green List (High Evidence).","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:54:52.531278+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.709","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB3 were changed from CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 2 to Cataract 22, MIM# 609741","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:51:19.755713+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB3 were set to ","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:51:08.146823+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.707","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB3 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:50:54.723980+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB3","entity_type":"gene"},{"created":"2021-11-25T17:48:23.582147+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB2 as ready","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:48:23.571867+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb2 has been classified as Green List (High Evidence).","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:47:43.043675+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB2 were changed from  to Cataract 3, multiple types, MIM# 601547","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:47:12.252828+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB2 were set to ","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:46:47.984807+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.308","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:46:17.744148+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:45:40.720780+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9871","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB2 as ready","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:45:40.710166+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9871","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb2 has been classified as Green List (High Evidence).","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:45:28.412090+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9871","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB2 were changed from  to Cataract 3, multiple types, MIM# 601547","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:45:11.462542+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9870","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB2 were set to ","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:44:52.612270+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9869","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:44:19.374034+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9868","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:43:34.052532+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB2 as ready","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:43:34.041662+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb2 has been classified as Green List (High Evidence).","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:43:30.587932+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB2 were changed from CATARACT, COPPOCK-LIKE; CATARACT, CONGENITAL, CERULEAN TYPE, 2 to Cataract 3, multiple types, MIM# 601547","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:43:10.614955+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.705","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB2 were set to ","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:42:59.033193+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.704","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:42:46.521845+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.703","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYBB2","entity_type":"gene"},{"created":"2021-11-25T17:40:23.711017+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB1 as ready","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:40:23.702041+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb1 has been classified as Green List (High Evidence).","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:34:32.370111+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB1 were changed from  to Cataract 17, multiple types, MIM# 611544","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:34:01.188896+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB1 were set to ","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:33:33.115544+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:33:05.399013+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:32:27.150215+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9868","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB1 as ready","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:32:27.141420+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9868","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb1 has been classified as Green List (High Evidence).","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:32:20.332901+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9868","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB1 were changed from  to Cataract 17, multiple types, MIM# 611544","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:32:02.041363+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9867","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB1 were set to ","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:31:40.977780+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9866","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYBB1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:31:22.893822+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9865","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:30:27.716797+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.703","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYBB1 as ready","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:30:27.707759+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.703","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crybb1 has been classified as Green List (High Evidence).","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:30:16.932414+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.703","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYBB1 were changed from CATARACT 17, MULTIPLE TYPES, MONOALLELIC; CATARACT 17, MULTIPLE TYPES; CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 3 to Cataract 17, multiple types, MIM# 611544","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:30:04.871871+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.702","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYBB1 were set to ","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T17:29:50.194166+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CRYBB1","entity_type":"gene"},{"created":"2021-11-25T12:38:48.616451+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9865","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFAIP3 as ready","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:38:48.602085+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9865","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfaip3 has been classified as Green List (High Evidence).","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:38:15.676891+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9865","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNFAIP3 were changed from  to Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744; Inflammatory bowel disease","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:37:53.277078+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9864","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFAIP3 were set to ","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:37:30.297439+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9863","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TNFAIP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:37:09.641038+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9862","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TNFAIP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26642243, 34030699, 33446651, 32521965, 31299923; Phenotypes: Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744, Inflammatory bowel disease; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:34:52.405154+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFAIP3 as ready","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:34:52.395537+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfaip3 has been classified as Green List (High Evidence).","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:34:49.815181+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNFAIP3 were changed from  to Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:34:25.022155+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFAIP3 were set to ","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:34:00.857516+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TNFAIP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:33:26.849894+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TNFAIP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26642243; Phenotypes: Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744; Mode of inheritance: None","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:27:03.967471+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFAIP3 as ready","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:27:03.956774+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfaip3 has been classified as Green List (High Evidence).","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:26:31.929996+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFAIP3 were set to 34030699, 33446651, 32521965, 31299923","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:25:59.386126+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TNFAIP3 as Green List (high evidence)","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T12:25:59.376747+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfaip3 has been classified as Green List (High Evidence).","entity_name":"TNFAIP3","entity_type":"gene"},{"created":"2021-11-25T11:54:15.370932+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9862","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SFTPA1 were changed from Idiopathic pulmonary fibrosis to Idiopathic pulmonary fibrosis; Interstitial lung disease 1, MIM#\t619611","entity_name":"SFTPA1","entity_type":"gene"},{"created":"2021-11-25T11:53:56.442274+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9861","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SFTPA1: Changed phenotypes: Idiopathic pulmonary fibrosis, Interstitial lung disease 1, MIM# 619611","entity_name":"SFTPA1","entity_type":"gene"},{"created":"2021-11-25T11:53:37.230166+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SFTPA1 were changed from Idiopathic pulmonary fibrosis to Idiopathic pulmonary fibrosis; Interstitial lung disease 1, MIM#\t619611","entity_name":"SFTPA1","entity_type":"gene"},{"created":"2021-11-25T11:53:02.311013+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SFTPA1: Changed phenotypes: Idiopathic pulmonary fibrosis, Interstitial lung disease 1, MIM# 619611","entity_name":"SFTPA1","entity_type":"gene"},{"created":"2021-11-25T11:51:34.350563+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9861","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PI4KA were changed from Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531; Neurodevelopmental syndrome with hypomyelinating leukodystrophy to Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531; Neurodevelopmental syndrome with hypomyelinating leukodystrophy; Spastic paraplegia 84, autosomal recessive, MIM# 619621","entity_name":"PI4KA","entity_type":"gene"},{"created":"2021-11-25T11:51:01.937024+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9860","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PI4KA: Changed phenotypes: Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531, Neurodevelopmental syndrome with hypomyelinating leukodystrophy, Spastic paraplegia 84, autosomal recessive, MIM# 619621","entity_name":"PI4KA","entity_type":"gene"},{"created":"2021-11-25T11:50:27.114220+11:00","panel_name":"Hereditary Spastic Paraplegia - paediatric","panel_id":317,"panel_version":"1.21","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PI4KA were changed from Neurodevelopmental syndrome with hypomyelinating leukodystrophy to Neurodevelopmental syndrome with hypomyelinating leukodystrophy; Spastic paraplegia 84, autosomal recessive, MIM# 619621","entity_name":"PI4KA","entity_type":"gene"},{"created":"2021-11-25T11:50:06.443189+11:00","panel_name":"Hereditary Spastic Paraplegia - paediatric","panel_id":317,"panel_version":"1.20","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PI4KA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 84, autosomal recessive, MIM# 619621; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PI4KA","entity_type":"gene"},{"created":"2021-11-25T11:47:57.031721+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9860","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UCP2 as ready","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:47:57.015561+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9860","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ucp2 has been classified as Amber List (Moderate Evidence).","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:47:31.691466+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9860","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UCP2 were changed from  to {Obesity, susceptibility to, BMIQ4} 607447; Hyperinsulinism","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:47:12.396974+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9859","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UCP2 were set to ","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:46:49.438196+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9858","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UCP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:46:29.149831+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9857","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UCP2 as Amber List (moderate evidence)","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:46:29.140141+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9857","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ucp2 has been classified as Amber List (Moderate Evidence).","entity_name":"UCP2","entity_type":"gene"},{"created":"2021-11-25T11:46:12.675538+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9856","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UCP2: Rating: AMBER; Mode of pathogenicity: None; Publications: 19065272, 11381268; Phenotypes: {Obesity, susceptibility to, BMIQ4} 607447, Hyperinsulinism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UCP2","entity_type":"gene"}]}