{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1076","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1074","results":[{"created":"2021-12-20T17:13:51.341874+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRDM6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Patent ductus arteriosus 3 - MIM#617039; Mode of inheritance: None","entity_name":"PRDM6","entity_type":"gene"},{"created":"2021-12-20T17:12:56.043128+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM126A as ready","entity_name":"FAM126A","entity_type":"gene"},{"created":"2021-12-20T17:12:56.020795+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam126a has been classified as Green List (High Evidence).","entity_name":"FAM126A","entity_type":"gene"},{"created":"2021-12-20T17:12:40.542290+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM126A were changed from LEUKODYSTROPHY HYPOMYELINATING TYPE 5 to Leukodystrophy, hypomyelinating, 5 MIM#610532","entity_name":"FAM126A","entity_type":"gene"},{"created":"2021-12-20T17:12:28.192205+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1507","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM126A were set to ","entity_name":"FAM126A","entity_type":"gene"},{"created":"2021-12-20T17:11:02.084882+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX2-6 as ready","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:11:02.073687+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-6 has been classified as Amber List (Moderate Evidence).","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:10:56.874905+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NKX2-6 were changed from  to Conotruncal heart malformations - MIM#217095; Persistent truncus arteriosus - MIM#217095","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:10:42.601175+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1505","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NKX2-6 as Amber List (moderate evidence)","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:10:42.590048+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-6 has been classified as Amber List (Moderate Evidence).","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:10:30.214999+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NKX2-6: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Conotruncal heart malformations - MIM#217095, Persistent truncus arteriosus - MIM#217095; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX2-6","entity_type":"gene"},{"created":"2021-12-20T17:09:29.886790+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT74 as ready","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:09:29.876673+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Red List (Low Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:09:25.949895+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT74 were changed from HYPOTRICHOSIS SIMPLEX OF THE SCALP 2 to Woolly hair, autosomal dominant (MIM#194300)","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:09:13.523840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT74 were set to ","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:09:02.449258+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1502","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT74 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:08:51.399295+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1501","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT74 as Red List (low evidence)","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:08:51.388188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1501","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Red List (Low Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2021-12-20T17:08:19.951714+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1500","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAH as ready","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:08:19.935916+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1500","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fah has been classified as Red List (Low Evidence).","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:08:14.285583+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1500","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: YY1 as ready","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:08:14.273297+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1500","user_name":"Alison Yeung","item_type":"entity","text":"Gene: yy1 has been classified as Green List (High Evidence).","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:08:13.442110+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1500","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAH were changed from TYROSINEMIA TYPE 1 to Tyrosinemia, type I, MIM#276700","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:08:00.747809+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1499","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAH were set to ","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:08:00.178509+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1499","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: YY1 were changed from INTELLECTUAL DISABILITY to Gabriele-de Vries syndrome, OMIM #617557","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:07:47.771811+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1498","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAH as Red List (low evidence)","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:07:47.759617+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1498","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fah has been classified as Red List (Low Evidence).","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:07:38.540103+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1497","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: YY1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:07:36.625064+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FAH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Tyrosinemia, type I, MIM#276700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAH","entity_type":"gene"},{"created":"2021-12-20T17:06:28.137489+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: YY1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575647; Phenotypes: Gabriele-de Vries syndrome, OMIM #617557; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:05:14.907226+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYBPC3 as ready","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2021-12-20T17:05:14.896203+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mybpc3 has been classified as Green List (High Evidence).","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2021-12-20T17:05:07.765515+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYBPC3 as Green List (high evidence)","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2021-12-20T17:05:07.754675+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1496","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mybpc3 has been classified as Green List (High Evidence).","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2021-12-20T17:04:11.054766+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1495","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNJ8 as ready","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2021-12-20T17:04:11.044309+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1495","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj8 has been classified as Green List (High Evidence).","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2021-12-20T17:04:03.144798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1495","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KCNJ8 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2021-12-20T17:03:20.656960+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: YY1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575647; Phenotypes: Gabriele-de Vries syndrome, OMIM #617557; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"YY1","entity_type":"gene"},{"created":"2021-12-20T17:02:33.011455+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1494","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNJ8 as Green List (high evidence)","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2021-12-20T17:02:32.993987+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj8 has been classified as Green List (High Evidence).","entity_name":"KCNJ8","entity_type":"gene"},{"created":"2021-12-20T17:00:58.548777+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1493","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MMP15 as ready","entity_name":"MMP15","entity_type":"gene"},{"created":"2021-12-20T17:00:58.537662+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1493","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mmp15 has been classified as Amber List (Moderate Evidence).","entity_name":"MMP15","entity_type":"gene"},{"created":"2021-12-20T17:00:51.700906+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1493","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MMP15 as Amber List (moderate evidence)","entity_name":"MMP15","entity_type":"gene"},{"created":"2021-12-20T17:00:51.691108+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1493","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mmp15 has been classified as Amber List (Moderate Evidence).","entity_name":"MMP15","entity_type":"gene"},{"created":"2021-12-20T17:00:21.087718+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1492","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIB1 as ready","entity_name":"MIB1","entity_type":"gene"},{"created":"2021-12-20T17:00:21.077422+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1492","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mib1 has been classified as Amber List (Moderate Evidence).","entity_name":"MIB1","entity_type":"gene"},{"created":"2021-12-20T17:00:14.037788+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1492","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIB1 as Amber List (moderate evidence)","entity_name":"MIB1","entity_type":"gene"},{"created":"2021-12-20T17:00:14.023937+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1492","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mib1 has been classified as Amber List (Moderate Evidence).","entity_name":"MIB1","entity_type":"gene"},{"created":"2021-12-20T16:59:39.307995+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MESP1 as ready","entity_name":"MESP1","entity_type":"gene"},{"created":"2021-12-20T16:59:39.289014+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mesp1 has been classified as Amber List (Moderate Evidence).","entity_name":"MESP1","entity_type":"gene"},{"created":"2021-12-20T16:59:33.300233+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MESP1 as Amber List (moderate evidence)","entity_name":"MESP1","entity_type":"gene"},{"created":"2021-12-20T16:59:33.290681+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mesp1 has been classified as Amber List (Moderate Evidence).","entity_name":"MESP1","entity_type":"gene"},{"created":"2021-12-20T16:58:38.398677+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSPA9 as ready","entity_name":"HSPA9","entity_type":"gene"},{"created":"2021-12-20T16:58:38.388832+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspa9 has been classified as Green List (High Evidence).","entity_name":"HSPA9","entity_type":"gene"},{"created":"2021-12-20T16:58:29.264090+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HSPA9 as Green List (high evidence)","entity_name":"HSPA9","entity_type":"gene"},{"created":"2021-12-20T16:58:29.252130+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspa9 has been classified as Green List (High Evidence).","entity_name":"HSPA9","entity_type":"gene"},{"created":"2021-12-20T16:54:12.371219+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: GM2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 28417072, 28192816, 27402091; Phenotypes: GM2-gangliosidosis, AB variant MIM#272750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"GM2A","entity_type":"gene"},{"created":"2021-12-20T16:53:49.446651+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FOXH1: Rating: RED; Mode of pathogenicity: None; Publications: 32003456; Phenotypes: Congenital heart disease; Mode of inheritance: None","entity_name":"FOXH1","entity_type":"gene"},{"created":"2021-12-20T16:52:18.887270+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: GM2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 28417072, 28192816, 27402091, 33819415; Phenotypes: GM2-gangliosidosis, AB variant MIM#272750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"GM2A","entity_type":"gene"},{"created":"2021-12-20T16:45:41.283045+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FBRSL1 as ready","entity_name":"FBRSL1","entity_type":"gene"},{"created":"2021-12-20T16:45:41.272515+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbrsl1 has been classified as Green List (High Evidence).","entity_name":"FBRSL1","entity_type":"gene"},{"created":"2021-12-20T16:45:34.284959+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FBRSL1 as Green List (high evidence)","entity_name":"FBRSL1","entity_type":"gene"},{"created":"2021-12-20T16:45:34.272614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1489","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbrsl1 has been classified as Green List (High Evidence).","entity_name":"FBRSL1","entity_type":"gene"},{"created":"2021-12-20T16:45:03.431773+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSTM1 as ready","entity_name":"OSTM1","entity_type":"gene"},{"created":"2021-12-20T16:45:03.409000+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ostm1 has been classified as Green List (High Evidence).","entity_name":"OSTM1","entity_type":"gene"},{"created":"2021-12-20T16:44:18.577586+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CITED2 as ready","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:44:18.568364+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cited2 has been classified as Green List (High Evidence).","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:44:12.773869+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1488","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CITED2 were set to 11694877; 16287139","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:43:58.020354+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CITED2 as Green List (high evidence)","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:43:58.009995+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cited2 has been classified as Green List (High Evidence).","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:43:37.721725+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CITED2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33706167, 33439552, 31515672, 29536580; Phenotypes: Atrial septal defect 8 - MIM#614433, Ventricular septal defect 2 - MIM#614431; Mode of inheritance: None","entity_name":"CITED2","entity_type":"gene"},{"created":"2021-12-20T16:40:19.179748+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BMPR2 as ready","entity_name":"BMPR2","entity_type":"gene"},{"created":"2021-12-20T16:40:19.169364+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bmpr2 has been classified as Red List (Low Evidence).","entity_name":"BMPR2","entity_type":"gene"},{"created":"2021-12-20T16:40:11.103403+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BMPR2 as Red List (low evidence)","entity_name":"BMPR2","entity_type":"gene"},{"created":"2021-12-20T16:40:11.091975+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bmpr2 has been classified as Red List (Low Evidence).","entity_name":"BMPR2","entity_type":"gene"},{"created":"2021-12-20T16:39:56.975226+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1485","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BMPR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"BMPR2","entity_type":"gene"},{"created":"2021-12-20T16:38:44.845806+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1485","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OPHN1 as ready","entity_name":"OPHN1","entity_type":"gene"},{"created":"2021-12-20T16:38:44.834968+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1485","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ophn1 has been classified as Green List (High Evidence).","entity_name":"OPHN1","entity_type":"gene"},{"created":"2021-12-20T16:38:44.365522+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1485","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSTM1 were changed from Osteopetrosis 259720 to Osteopetrosis, autosomal recessive 5 (MIM#259720)","entity_name":"OSTM1","entity_type":"gene"},{"created":"2021-12-20T16:38:32.592621+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1484","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSTM1 were set to ","entity_name":"OSTM1","entity_type":"gene"},{"created":"2021-12-20T16:37:54.738742+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OCLN as ready","entity_name":"OCLN","entity_type":"gene"},{"created":"2021-12-20T16:37:54.728920+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ocln has been classified as Green List (High Evidence).","entity_name":"OCLN","entity_type":"gene"},{"created":"2021-12-20T16:37:52.540642+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OPHN1 were changed from Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 to Intellectual developmental disorder, X-linked syndromic, Billuart type (MIM#300486)","entity_name":"OPHN1","entity_type":"gene"},{"created":"2021-12-20T16:37:38.863851+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1482","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OPHN1 were set to ","entity_name":"OPHN1","entity_type":"gene"},{"created":"2021-12-20T16:36:55.902708+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1481","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OBSL1 as ready","entity_name":"OBSL1","entity_type":"gene"},{"created":"2021-12-20T16:36:55.887098+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1481","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: obsl1 has been classified as Green List (High Evidence).","entity_name":"OBSL1","entity_type":"gene"},{"created":"2021-12-20T16:36:53.887945+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1481","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OCLN were changed from Band-like calcification with simplified gyration and polymicrogyria 251290 to Pseudo-TORCH syndrome 1 (MIM#251290)","entity_name":"OCLN","entity_type":"gene"},{"created":"2021-12-20T16:36:40.181579+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1480","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OCLN were set to ","entity_name":"OCLN","entity_type":"gene"},{"created":"2021-12-20T16:36:09.947110+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1479","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OBSL1 were changed from 3-M SYNDROME 2 to 3-M syndrome 2 (MIM#612921)","entity_name":"OBSL1","entity_type":"gene"},{"created":"2021-12-20T16:36:01.538837+11:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.243","user_name":"Ain Roesley","item_type":"entity","text":"gene: GLI1 was added\ngene: GLI1 was added to Polydactyly. Sources: Literature\nMode of inheritance for gene: GLI1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GLI1 were set to 34721536; 31621941; 31549748; 30620395\nPhenotypes for gene: GLI1 were set to Polydactyly, postaxial, type A8 MIM#618123; Polydactyly, preaxial I MIM#174400\nPenetrance for gene: GLI1 were set to unknown\nReview for gene: GLI1 was set to GREEN\ngene: GLI1 was marked as current diagnostic\nAdded comment: >10 unrelated probands reported, both AD and AR reported \nSources: Literature","entity_name":"GLI1","entity_type":"gene"},{"created":"2021-12-20T16:36:00.925987+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1478","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OBSL1 were set to ","entity_name":"OBSL1","entity_type":"gene"},{"created":"2021-12-20T16:35:18.158690+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NR0B1 as ready","entity_name":"NR0B1","entity_type":"gene"},{"created":"2021-12-20T16:35:18.144236+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nr0b1 has been classified as Amber List (Moderate Evidence).","entity_name":"NR0B1","entity_type":"gene"},{"created":"2021-12-20T16:35:17.943969+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: GLI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 34721536, 31621941, 31549748, 30620395; Phenotypes: Polydactyly, postaxial, type A8 MIM#618123, Polydactyly, preaxial I MIM#174400; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"GLI1","entity_type":"gene"},{"created":"2021-12-20T16:35:14.838181+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUBPL as ready","entity_name":"NUBPL","entity_type":"gene"},{"created":"2021-12-20T16:35:14.809153+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nubpl has been classified as Green List (High Evidence).","entity_name":"NUBPL","entity_type":"gene"},{"created":"2021-12-20T16:35:13.804074+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Ain Roesley","item_type":"entity","text":"gene: GLI1 was added\ngene: GLI1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: GLI1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GLI1 were set to 34721536; 31621941; 31549748; 30620395\nPhenotypes for gene: GLI1 were set to Polydactyly, postaxial, type A8\tMIM#618123; Polydactyly, preaxial I\tMIM#174400\nPenetrance for gene: GLI1 were set to unknown\nReview for gene: GLI1 was set to GREEN\ngene: GLI1 was marked as current diagnostic\nAdded comment: >10 unrelated probands reported, both AD and AR reported \nSources: Literature","entity_name":"GLI1","entity_type":"gene"},{"created":"2021-12-20T16:35:07.860148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1477","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUBPL were changed from MITOCHONDRIAL COMPLEX I DEFICIENCY to Mitochondrial complex I deficiency, nuclear type 21 (MIM#618242)","entity_name":"NUBPL","entity_type":"gene"},{"created":"2021-12-20T16:34:55.343998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1476","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUBPL were set to ","entity_name":"NUBPL","entity_type":"gene"},{"created":"2021-12-20T16:34:23.806985+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1475","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NR5A1 as ready","entity_name":"NR5A1","entity_type":"gene"}]}