{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1033","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1031","results":[{"created":"2022-01-21T10:38:09.121755+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10726","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKBP10 as ready","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:38:09.104813+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10726","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp10 has been classified as Green List (High Evidence).","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:35:14.667244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10726","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKBP10 were changed from  to Bruck syndrome 1, MONDO:0009806; Osteogenesis imperfecta, type XI, OMIM:610968; Osteogenesis imperfecta type 11, MONDO:0012592; Bruck syndrome 1, OMIM:259450","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:34:55.410949+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10725","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKBP10 were set to ","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:34:37.164012+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10724","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FKBP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:33:53.211732+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10723","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FKBP10: Rating: GREEN; Mode of pathogenicity: None; Publications: 20696291, 20362275, 20839288, 21567934, 21567934, 23712425, 22718341; Phenotypes: Bruck syndrome 1, MONDO:0009806, Osteogenesis imperfecta, type XI, OMIM:610968, Osteogenesis imperfecta type 11, MONDO:0012592, Bruck syndrome 1, OMIM:259450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:33:08.873586+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2648","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKBP10 as ready","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:33:08.862962+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2648","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp10 has been classified as Green List (High Evidence).","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:32:48.922820+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2648","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKBP10 were set to ","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:28:24.694066+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2647","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FKBP10 as Green List (high evidence)","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:28:24.683576+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2647","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp10 has been classified as Green List (High Evidence).","entity_name":"FKBP10","entity_type":"gene"},{"created":"2022-01-21T10:27:27.268548+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2646","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF9 as ready","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:27:27.258842+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2646","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf9 has been classified as Green List (High Evidence).","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:27:23.458659+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2646","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGF9 were changed from MULTIPLE SYNOSTOSES SYNDROME TYPE 3 to Multiple synostoses syndrome 3, OMIM # 612961; Craniosynostosis","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:27:10.201798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2645","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGF9 were set to ","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:26:56.789421+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2644","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGF9 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:26:45.707961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2643","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGF9 as Green List (high evidence)","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:26:45.697064+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2643","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf9 has been classified as Green List (High Evidence).","entity_name":"FGF9","entity_type":"gene"},{"created":"2022-01-21T10:24:51.009265+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10723","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM46A as ready","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:24:50.990323+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10723","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam46a has been classified as Green List (High Evidence).","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:24:42.607787+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10723","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM46A were changed from  to Osteogenesis imperfecta, type XVIII MIM#617952","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:24:19.376129+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10722","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM46A were set to ","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:24:01.882564+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10721","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FAM46A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:23:42.449322+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10720","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: FAM46A.","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:23:11.275961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2642","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: FAM46A.","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:15:46.081148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2642","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM46A as ready","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:15:46.070509+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2642","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam46a has been classified as Green List (High Evidence).","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:15:40.367998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2642","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM46A were set to ","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:15:28.307419+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2641","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAM46A as Green List (high evidence)","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:15:28.296036+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2641","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam46a has been classified as Green List (High Evidence).","entity_name":"FAM46A","entity_type":"gene"},{"created":"2022-01-21T10:14:44.146890+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10720","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DYNC1I1 as ready","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:14:44.136187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10720","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dync1i1 has been classified as Green List (High Evidence).","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:14:34.775814+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10720","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DYNC1I1 as Green List (high evidence)","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:14:34.765400+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10720","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dync1i1 has been classified as Green List (High Evidence).","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:14:17.700585+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10719","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: DYNC1I1.","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:13:56.084444+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DYNC1I1 as ready","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:13:56.074491+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dync1i1 has been classified as Green List (High Evidence).","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:13:39.608664+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DYNC1I1 as Green List (high evidence)","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:13:39.596733+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dync1i1 has been classified as Green List (High Evidence).","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:13:30.171156+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2639","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: DYNC1I1.","entity_name":"DYNC1I1","entity_type":"gene"},{"created":"2022-01-21T10:12:29.572877+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10719","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA5 as ready","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:12:29.555219+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10719","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:12:21.219406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10719","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA5 were changed from  to Congenital heart defects, multiple types, 5 - #617912","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:11:56.816069+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10718","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GATA5 were set to ","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:11:37.310657+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10717","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GATA5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:11:18.336753+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10716","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA5 as Amber List (moderate evidence)","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:11:18.326185+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10716","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:10:50.790035+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA5 as ready","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:10:50.775970+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:10:46.230861+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA5 were changed from  to Congenital heart defects, multiple types, 5 - #617912","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:10:16.478526+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GATA5 were set to ","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:09:51.622423+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GATA5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:09:23.294272+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA5 as Amber List (moderate evidence)","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:09:23.284087+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:08:41.464135+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2639","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA5 as ready","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:08:41.452125+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2639","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:08:36.565926+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2639","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA5 were changed from Congenital heart defects, multiple types, 5 - #617912 to Congenital heart defects, multiple types, 5 - MIM#617912","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:08:25.870156+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2638","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GATA5 were set to 27066509; 23289003; 22961344; 23031282","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:07:57.470782+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2637","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA5 as Amber List (moderate evidence)","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:07:57.444409+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2637","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata5 has been classified as Amber List (Moderate Evidence).","entity_name":"GATA5","entity_type":"gene"},{"created":"2022-01-21T10:06:22.617366+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2636","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYPN as ready","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:06:22.606887+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2636","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mypn has been classified as Red List (Low Evidence).","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:06:18.890828+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2636","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYPN were changed from Nemaline myopathy 11, autosomal recessive, 617336 to Nemaline myopathy 11, autosomal recessive, MIM# 617336","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:06:03.366121+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2635","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYPN were set to ","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:05:50.102543+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2634","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYPN as Red List (low evidence)","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:05:50.093535+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2634","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mypn has been classified as Red List (Low Evidence).","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:05:36.580676+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2633","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYPN: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 11, autosomal recessive MIM#617336; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:04:20.305900+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.685","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: UQCRC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33865955; Phenotypes: motor delay, developmental delay, symmetric necrotic lesions in the brain stem suggesting Leigh-like syndrome, strabismus, cerebellar signs, lactic academia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UQCRC2","entity_type":"gene"},{"created":"2022-01-21T10:04:18.304550+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10715","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYPN as ready","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:04:18.287219+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10715","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mypn has been classified as Green List (High Evidence).","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:04:10.737804+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10715","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYPN were changed from  to Nemaline myopathy 11, autosomal recessive MIM#617336 AR; cardiomyopathy MIM#615248 AD","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:03:48.166410+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10714","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYPN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MYPN","entity_type":"gene"},{"created":"2022-01-21T10:02:56.707262+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2633","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYOD1 as ready","entity_name":"MYOD1","entity_type":"gene"},{"created":"2022-01-21T10:02:56.697102+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2633","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myod1 has been classified as Green List (High Evidence).","entity_name":"MYOD1","entity_type":"gene"},{"created":"2022-01-21T10:02:48.125916+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2633","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYOD1 as Green List (high evidence)","entity_name":"MYOD1","entity_type":"gene"},{"created":"2022-01-21T10:02:48.113530+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2633","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myod1 has been classified as Green List (High Evidence).","entity_name":"MYOD1","entity_type":"gene"},{"created":"2022-01-21T10:02:16.714018+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2632","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO18B as ready","entity_name":"MYO18B","entity_type":"gene"},{"created":"2022-01-21T10:02:16.701884+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2632","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo18b has been classified as Green List (High Evidence).","entity_name":"MYO18B","entity_type":"gene"},{"created":"2022-01-21T10:02:12.165125+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2632","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO18B were set to 27858739; 25748484; 27879346","entity_name":"MYO18B","entity_type":"gene"},{"created":"2022-01-21T10:01:11.822516+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2631","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYO18B as Green List (high evidence)","entity_name":"MYO18B","entity_type":"gene"},{"created":"2022-01-21T10:01:11.812902+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2631","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo18b has been classified as Green List (High Evidence).","entity_name":"MYO18B","entity_type":"gene"},{"created":"2022-01-21T10:00:05.311100+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2630","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYLK as ready","entity_name":"MYLK","entity_type":"gene"},{"created":"2022-01-21T10:00:05.296903+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2630","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mylk has been classified as Amber List (Moderate Evidence).","entity_name":"MYLK","entity_type":"gene"},{"created":"2022-01-21T09:59:58.524044+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2630","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYLK were changed from MMIH; Megacystis Microcolon Intestinal Hypoperistalsis Syndrome to Megacystis-microcolon-intestinal hypoperistalsis syndrome 1 MIM#249210","entity_name":"MYLK","entity_type":"gene"},{"created":"2022-01-21T09:53:13.686183+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2629","user_name":"Ain Roesley","item_type":"entity","text":"edited their review of gene: MECR: Changed phenotypes: Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities MIM#617282","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:28:47.458211+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2629","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYL9 as ready","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:28:47.446347+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2629","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl9 has been classified as Green List (High Evidence).","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:28:42.144492+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2629","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYL9 were changed from Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIH) to Megacystis-microcolon-intestinal hypoperistalsis syndrome, MIM#619365","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:28:29.345743+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2628","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYL9 were set to 29453416; 33031641","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:28:15.784109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2627","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYL9 as Green List (high evidence)","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:28:15.765494+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2627","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl9 has been classified as Green List (High Evidence).","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:27:53.656751+11:00","panel_name":"Gastrointestinal neuromuscular disease","panel_id":3087,"panel_version":"1.17","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYL9 were set to 29453416; 33031641","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:27:42.300757+11:00","panel_name":"Gastrointestinal neuromuscular disease","panel_id":3087,"panel_version":"1.16","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYL9 as Green List (high evidence)","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:27:42.289747+11:00","panel_name":"Gastrointestinal neuromuscular disease","panel_id":3087,"panel_version":"1.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl9 has been classified as Green List (High Evidence).","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:27:27.793598+11:00","panel_name":"Gastrointestinal neuromuscular disease","panel_id":3087,"panel_version":"1.15","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MYL9: Added comment: PMID:32621347; 3rd family with non-consanguineous parents and 3 TOPs.; Changed rating: GREEN; Changed publications: 33031641, 32621347","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:23:14.730966+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10713","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYL9 were set to 29453416; 33031641","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:22:39.909885+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10712","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYL9 as Green List (high evidence)","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:22:39.898958+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10712","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl9 has been classified as Green List (High Evidence).","entity_name":"MYL9","entity_type":"gene"},{"created":"2022-01-21T09:20:48.175876+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10711","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSTO1 as ready","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:20:48.166548+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10711","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msto1 has been classified as Green List (High Evidence).","entity_name":"MSTO1","entity_type":"gene"}]}