{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1075","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1073","results":[{"created":"2021-12-20T17:41:55.090261+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1539","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: WNT10B as ready","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:41:55.080235+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1539","user_name":"Alison Yeung","item_type":"entity","text":"Gene: wnt10b has been classified as Green List (High Evidence).","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:41:36.163910+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1539","user_name":"Alison Yeung","item_type":"entity","text":"Classified gene: WNT10B as Green List (high evidence)","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:41:36.152196+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1539","user_name":"Alison Yeung","item_type":"entity","text":"Gene: wnt10b has been classified as Green List (High Evidence).","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:41:09.487410+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1538","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: WNT10B: Rating: GREEN; Mode of pathogenicity: None; Publications: 20635353, 24211389, 27321946; Phenotypes: Split-hand/foot malformation 6, OMIM #601906; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:36:09.592724+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: WNT10B as ready","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:36:09.582190+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Alison Yeung","item_type":"entity","text":"Gene: wnt10b has been classified as Green List (High Evidence).","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:35:32.377025+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: WNT10B: Rating: GREEN; Mode of pathogenicity: None; Publications: 20635353, 24211389, 27321946; Phenotypes: Split-hand/foot malformation 6, OMIM #601906, Tooth agenesis, selective, 8, OMIM #617073; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-12-20T17:32:27.485265+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRB2 as ready","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:32:27.473568+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb2 has been classified as Green List (High Evidence).","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:32:23.743989+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GANAB was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GANAB","entity_type":"gene"},{"created":"2021-12-20T17:32:13.289639+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GANAB as Red List (low evidence)","entity_name":"GANAB","entity_type":"gene"},{"created":"2021-12-20T17:32:13.278093+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ganab has been classified as Red List (Low Evidence).","entity_name":"GANAB","entity_type":"gene"},{"created":"2021-12-20T17:31:58.582727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1536","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GANAB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Polycystic kidney disease 3, MIM#600666; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GANAB","entity_type":"gene"},{"created":"2021-12-20T17:30:45.961462+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1536","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GABRB2 were changed from Epilepsy and intellectual disability to Developmental and epileptic encephalopathy 92 MIM#617829","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:30:12.999626+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1535","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GABRB2 were set to ","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:30:01.693273+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1534","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: GABRB2 was changed from  to Other","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:29:49.508688+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GABRB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:29:39.734670+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GABRB2 as Green List (high evidence)","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:29:39.724183+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb2 has been classified as Green List (High Evidence).","entity_name":"GABRB2","entity_type":"gene"},{"created":"2021-12-20T17:29:14.663943+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF699 as ready","entity_name":"ZNF699","entity_type":"gene"},{"created":"2021-12-20T17:29:14.652886+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf699 has been classified as Green List (High Evidence).","entity_name":"ZNF699","entity_type":"gene"},{"created":"2021-12-20T17:29:08.616257+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF699 as Green List (high evidence)","entity_name":"ZNF699","entity_type":"gene"},{"created":"2021-12-20T17:29:08.606397+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf699 has been classified as Green List (High Evidence).","entity_name":"ZNF699","entity_type":"gene"},{"created":"2021-12-20T17:28:37.457173+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZMYM2 as ready","entity_name":"ZMYM2","entity_type":"gene"},{"created":"2021-12-20T17:28:37.440416+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zmym2 has been classified as Green List (High Evidence).","entity_name":"ZMYM2","entity_type":"gene"},{"created":"2021-12-20T17:28:26.395432+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZMYM2 as Green List (high evidence)","entity_name":"ZMYM2","entity_type":"gene"},{"created":"2021-12-20T17:28:26.384718+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zmym2 has been classified as Green List (High Evidence).","entity_name":"ZMYM2","entity_type":"gene"},{"created":"2021-12-20T17:28:01.429649+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBR7 as ready","entity_name":"UBR7","entity_type":"gene"},{"created":"2021-12-20T17:28:01.420000+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ubr7 has been classified as Green List (High Evidence).","entity_name":"UBR7","entity_type":"gene"},{"created":"2021-12-20T17:27:55.785459+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UBR7 as Green List (high evidence)","entity_name":"UBR7","entity_type":"gene"},{"created":"2021-12-20T17:27:55.774864+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ubr7 has been classified as Green List (High Evidence).","entity_name":"UBR7","entity_type":"gene"},{"created":"2021-12-20T17:27:44.617844+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TLL1 were changed from  to Atrial septal defect 6 MIM#613087","entity_name":"TLL1","entity_type":"gene"},{"created":"2021-12-20T17:27:26.052630+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TLL1 as ready","entity_name":"TLL1","entity_type":"gene"},{"created":"2021-12-20T17:27:26.040445+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tll1 has been classified as Green List (High Evidence).","entity_name":"TLL1","entity_type":"gene"},{"created":"2021-12-20T17:27:04.346364+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TLL1 as Green List (high evidence)","entity_name":"TLL1","entity_type":"gene"},{"created":"2021-12-20T17:27:04.335210+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tll1 has been classified as Green List (High Evidence).","entity_name":"TLL1","entity_type":"gene"},{"created":"2021-12-20T17:26:28.789679+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX2 as ready","entity_name":"TBX2","entity_type":"gene"},{"created":"2021-12-20T17:26:28.778915+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx2 has been classified as Amber List (Moderate Evidence).","entity_name":"TBX2","entity_type":"gene"},{"created":"2021-12-20T17:26:20.792163+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TBX2 as Amber List (moderate evidence)","entity_name":"TBX2","entity_type":"gene"},{"created":"2021-12-20T17:26:20.782035+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx2 has been classified as Amber List (Moderate Evidence).","entity_name":"TBX2","entity_type":"gene"},{"created":"2021-12-20T17:26:08.676802+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBX2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Vertebral anomalies and variable endocrine and T-cell dysfunction - MIM#618223; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBX2","entity_type":"gene"},{"created":"2021-12-20T17:25:10.149265+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM58A as ready","entity_name":"FAM58A","entity_type":"gene"},{"created":"2021-12-20T17:25:10.139514+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam58a has been classified as Green List (High Evidence).","entity_name":"FAM58A","entity_type":"gene"},{"created":"2021-12-20T17:25:05.841326+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM58A were changed from STAR SYNDROME to STAR syndrome MIM#300707","entity_name":"FAM58A","entity_type":"gene"},{"created":"2021-12-20T17:24:53.765585+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM58A were set to ","entity_name":"FAM58A","entity_type":"gene"},{"created":"2021-12-20T17:24:50.897340+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1524","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: WRAP53 as ready","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:24:50.886767+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1524","user_name":"Alison Yeung","item_type":"entity","text":"Gene: wrap53 has been classified as Red List (Low Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:24:40.037043+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1524","user_name":"Alison Yeung","item_type":"entity","text":"Classified gene: WRAP53 as Red List (low evidence)","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:24:40.031962+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1524","user_name":"Alison Yeung","item_type":"entity","text":"Added comment: Comment on list classification: Not suitable for fetal anomalies list","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:24:39.994999+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1524","user_name":"Alison Yeung","item_type":"entity","text":"Gene: wrap53 has been classified as Red List (Low Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:24:22.879675+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STK4 as ready","entity_name":"STK4","entity_type":"gene"},{"created":"2021-12-20T17:24:22.869670+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stk4 has been classified as Green List (High Evidence).","entity_name":"STK4","entity_type":"gene"},{"created":"2021-12-20T17:24:16.671378+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: STK4 as Green List (high evidence)","entity_name":"STK4","entity_type":"gene"},{"created":"2021-12-20T17:24:16.661837+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stk4 has been classified as Green List (High Evidence).","entity_name":"STK4","entity_type":"gene"},{"created":"2021-12-20T17:23:43.272294+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPRED2 as ready","entity_name":"SPRED2","entity_type":"gene"},{"created":"2021-12-20T17:23:43.236444+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spred2 has been classified as Green List (High Evidence).","entity_name":"SPRED2","entity_type":"gene"},{"created":"2021-12-20T17:23:36.681096+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPRED2 as Green List (high evidence)","entity_name":"SPRED2","entity_type":"gene"},{"created":"2021-12-20T17:23:36.671661+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spred2 has been classified as Green List (High Evidence).","entity_name":"SPRED2","entity_type":"gene"},{"created":"2021-12-20T17:23:10.761721+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1521","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPEN as ready","entity_name":"SPEN","entity_type":"gene"},{"created":"2021-12-20T17:23:10.750372+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1521","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spen has been classified as Green List (High Evidence).","entity_name":"SPEN","entity_type":"gene"},{"created":"2021-12-20T17:23:03.728097+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1521","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPEN as Green List (high evidence)","entity_name":"SPEN","entity_type":"gene"},{"created":"2021-12-20T17:23:03.713623+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1521","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spen has been classified as Green List (High Evidence).","entity_name":"SPEN","entity_type":"gene"},{"created":"2021-12-20T17:22:34.956536+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1520","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMAD6 as ready","entity_name":"SMAD6","entity_type":"gene"},{"created":"2021-12-20T17:22:34.938658+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1520","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smad6 has been classified as Green List (High Evidence).","entity_name":"SMAD6","entity_type":"gene"},{"created":"2021-12-20T17:22:28.378271+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1520","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMAD6 as Green List (high evidence)","entity_name":"SMAD6","entity_type":"gene"},{"created":"2021-12-20T17:22:28.368176+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1520","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smad6 has been classified as Green List (High Evidence).","entity_name":"SMAD6","entity_type":"gene"},{"created":"2021-12-20T17:21:42.657651+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1519","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM20C as ready","entity_name":"FAM20C","entity_type":"gene"},{"created":"2021-12-20T17:21:42.647792+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1519","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam20c has been classified as Green List (High Evidence).","entity_name":"FAM20C","entity_type":"gene"},{"created":"2021-12-20T17:21:38.883996+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1519","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM20C were changed from RAINE SYNDROME to Raine syndrome MIM#259775","entity_name":"FAM20C","entity_type":"gene"},{"created":"2021-12-20T17:21:27.054814+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1518","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM20C were set to ","entity_name":"FAM20C","entity_type":"gene"},{"created":"2021-12-20T17:20:46.747465+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1517","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO4 as ready","entity_name":"ROBO4","entity_type":"gene"},{"created":"2021-12-20T17:20:46.735689+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1517","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Amber List (Moderate Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2021-12-20T17:20:39.395252+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1517","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ROBO4 as Amber List (moderate evidence)","entity_name":"ROBO4","entity_type":"gene"},{"created":"2021-12-20T17:20:39.384171+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1517","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Amber List (Moderate Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2021-12-20T17:20:26.554939+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1516","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ROBO4: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ROBO4","entity_type":"gene"},{"created":"2021-12-20T17:18:51.741695+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1516","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKACB as ready","entity_name":"PRKACB","entity_type":"gene"},{"created":"2021-12-20T17:18:51.732217+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1516","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkacb has been classified as Green List (High Evidence).","entity_name":"PRKACB","entity_type":"gene"},{"created":"2021-12-20T17:18:46.281318+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1516","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRKACB as Green List (high evidence)","entity_name":"PRKACB","entity_type":"gene"},{"created":"2021-12-20T17:18:46.267696+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1516","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkacb has been classified as Green List (High Evidence).","entity_name":"PRKACB","entity_type":"gene"},{"created":"2021-12-20T17:18:23.750804+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1515","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKACA as ready","entity_name":"PRKACA","entity_type":"gene"},{"created":"2021-12-20T17:18:23.740216+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1515","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkaca has been classified as Green List (High Evidence).","entity_name":"PRKACA","entity_type":"gene"},{"created":"2021-12-20T17:18:19.344149+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1515","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: WRAP53: Rating: RED; Mode of pathogenicity: None; Publications: 21205863, 32303682, 29514627; Phenotypes: Dyskeratosis congenita, autosomal recessive 3, OMIM #613988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-12-20T17:18:16.078219+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1515","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRKACA as Green List (high evidence)","entity_name":"PRKACA","entity_type":"gene"},{"created":"2021-12-20T17:18:16.064538+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1515","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkaca has been classified as Green List (High Evidence).","entity_name":"PRKACA","entity_type":"gene"},{"created":"2021-12-20T17:17:43.746407+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1514","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM20A as ready","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:17:43.732951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam20a has been classified as Red List (Low Evidence).","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:17:39.371496+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1514","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM20A were changed from AMELOGENESIS IMPERFECTA AND GINGIVAL FIBROMATOSIS SYNDROME to Amelogenesis imperfecta, type IG (enamel-renal syndrome) 204690","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:17:26.057522+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1513","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM20A were set to ","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:17:13.480025+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1512","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAM20A as Red List (low evidence)","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:17:13.466519+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam20a has been classified as Red List (Low Evidence).","entity_name":"FAM20A","entity_type":"gene"},{"created":"2021-12-20T17:16:06.800841+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10312","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: FAM126A: Rating: GREEN; Mode of pathogenicity: None; Publications: 21911699, 17928815, 17683097, 16951682; Phenotypes: Leukodystrophy, hypomyelinating, 5 MIM#610532; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"FAM126A","entity_type":"gene"},{"created":"2021-12-20T17:15:51.352880+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1511","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LINS1 as ready","entity_name":"LINS1","entity_type":"gene"},{"created":"2021-12-20T17:15:51.343615+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1511","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lins1 has been classified as Amber List (Moderate Evidence).","entity_name":"LINS1","entity_type":"gene"},{"created":"2021-12-20T17:15:45.793788+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1511","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LINS1 were changed from AUTOSOMAL RECESSIVE MENTAL RETARDATION to Mental retardation, autosomal recessive 27 (MIM#614340); autosomal recessive intellectual disability (MIM#614340)","entity_name":"LINS1","entity_type":"gene"},{"created":"2021-12-20T17:15:33.734617+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1510","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LINS1 were set to ","entity_name":"LINS1","entity_type":"gene"},{"created":"2021-12-20T17:14:12.694435+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1509","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRDM6 as ready","entity_name":"PRDM6","entity_type":"gene"},{"created":"2021-12-20T17:14:12.683242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1509","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prdm6 has been classified as Red List (Low Evidence).","entity_name":"PRDM6","entity_type":"gene"},{"created":"2021-12-20T17:14:04.850716+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1509","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRDM6 as Red List (low evidence)","entity_name":"PRDM6","entity_type":"gene"},{"created":"2021-12-20T17:14:04.832065+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1509","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prdm6 has been classified as Red List (Low Evidence).","entity_name":"PRDM6","entity_type":"gene"}]}