{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1120","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1118","results":[{"created":"2021-11-22T21:26:16.088164+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9843","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DVL3 as ready","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:26:16.077295+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9843","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dvl3 has been classified as Green List (High Evidence).","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:26:08.706194+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9843","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DVL3 were changed from  to Robinow syndrome, autosomal dominant 3 MIM#616894","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:25:47.904657+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9842","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DVL3 were set to ","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:25:25.948096+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9841","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DVL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:25:07.891042+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9840","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DVL3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26924530; Phenotypes: Robinow syndrome, autosomal dominant 3 MIM#616894; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:24:56.089837+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DVL3 as ready","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:24:56.080030+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dvl3 has been classified as Green List (High Evidence).","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:24:52.212611+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.684","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DVL3 were changed from AUTOSOMAL-DOMINANT ROBINOW SYNDROME to Robinow syndrome, autosomal dominant 3 MIM#616894","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:24:39.660317+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.683","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DVL3 were set to ","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:24:11.934728+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.682","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DVL3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DVL3","entity_type":"gene"},{"created":"2021-11-22T21:23:19.809837+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.681","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EN1 as ready","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:23:19.799625+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.681","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: en1 has been classified as Green List (High Evidence).","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:23:14.919283+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.681","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: EN1.\nTag 5'UTR tag was added to gene: EN1.","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:22:49.546275+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.681","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EN1 were changed from ?ENDOVE syndrome, limb-brain type - OMIM#619218 to ENDOVE syndrome, limb-brain type - OMIM#619218","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:22:37.626881+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.680","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EN1 as Green List (high evidence)","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:22:37.615825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.680","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: en1 has been classified as Green List (High Evidence).","entity_name":"EN1","entity_type":"gene"},{"created":"2021-11-22T21:21:58.233572+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.679","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC30A5 as ready","entity_name":"SLC30A5","entity_type":"gene"},{"created":"2021-11-22T21:21:58.223380+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.679","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc30a5 has been classified as Amber List (Moderate Evidence).","entity_name":"SLC30A5","entity_type":"gene"},{"created":"2021-11-22T21:21:51.208502+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.679","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC30A5 as Amber List (moderate evidence)","entity_name":"SLC30A5","entity_type":"gene"},{"created":"2021-11-22T21:21:51.195443+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.679","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc30a5 has been classified as Amber List (Moderate Evidence).","entity_name":"SLC30A5","entity_type":"gene"},{"created":"2021-11-22T21:21:13.744830+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.678","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SCN5A as ready","entity_name":"SCN5A","entity_type":"gene"},{"created":"2021-11-22T21:21:13.726343+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.678","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: scn5a has been classified as Green List (High Evidence).","entity_name":"SCN5A","entity_type":"gene"},{"created":"2021-11-22T21:21:07.403718+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.678","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SCN5A as Green List (high evidence)","entity_name":"SCN5A","entity_type":"gene"},{"created":"2021-11-22T21:21:07.393060+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.678","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: scn5a has been classified as Green List (High Evidence).","entity_name":"SCN5A","entity_type":"gene"},{"created":"2021-11-22T21:20:42.720127+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.677","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRF1 as ready","entity_name":"PRF1","entity_type":"gene"},{"created":"2021-11-22T21:20:42.708418+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.677","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prf1 has been classified as Green List (High Evidence).","entity_name":"PRF1","entity_type":"gene"},{"created":"2021-11-22T21:20:39.096880+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.677","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRF1 were changed from Aplastic anemia - #609135; Hemophagocytic lymphohistiocytosis, familial, 2 - #603553 to Aplastic anaemia - #609135; Haemophagocytic lymphohistiocytosis, familial, 2 - #603553","entity_name":"PRF1","entity_type":"gene"},{"created":"2021-11-22T21:20:21.411273+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.676","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRF1 as Green List (high evidence)","entity_name":"PRF1","entity_type":"gene"},{"created":"2021-11-22T21:20:21.402386+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.676","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prf1 has been classified as Green List (High Evidence).","entity_name":"PRF1","entity_type":"gene"},{"created":"2021-11-22T21:19:51.396160+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.675","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA1 as ready","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:19:51.384815+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.675","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Green List (High Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:19:46.699302+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.675","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA1 were changed from Anaemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835 to Anaemia, X-linked, with/without neutropaenia and/or platelet abnormalities, MIM#300835","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:19:35.837484+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.674","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA1 were changed from Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835 to Anaemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:19:19.964141+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.673","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA1 as Green List (high evidence)","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:19:19.953363+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.673","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Green List (High Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2021-11-22T21:18:45.352606+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.672","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALPK3 as ready","entity_name":"ALPK3","entity_type":"gene"},{"created":"2021-11-22T21:18:45.342820+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.672","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alpk3 has been classified as Green List (High Evidence).","entity_name":"ALPK3","entity_type":"gene"},{"created":"2021-11-22T21:18:39.802897+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.672","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ALPK3 as Green List (high evidence)","entity_name":"ALPK3","entity_type":"gene"},{"created":"2021-11-22T21:18:39.792396+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.672","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alpk3 has been classified as Green List (High Evidence).","entity_name":"ALPK3","entity_type":"gene"},{"created":"2021-11-22T21:18:13.503380+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.671","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZBTB42 as ready","entity_name":"ZBTB42","entity_type":"gene"},{"created":"2021-11-22T21:18:13.491363+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.671","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb42 has been classified as Amber List (Moderate Evidence).","entity_name":"ZBTB42","entity_type":"gene"},{"created":"2021-11-22T21:18:09.553279+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.671","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZBTB42 were changed from ?Lethal congenital contracture syndrome 6- #616248 to Lethal congenital contracture syndrome 6- #616248","entity_name":"ZBTB42","entity_type":"gene"},{"created":"2021-11-22T21:17:58.043469+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.670","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZBTB42 as Amber List (moderate evidence)","entity_name":"ZBTB42","entity_type":"gene"},{"created":"2021-11-22T21:17:58.033267+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.670","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb42 has been classified as Amber List (Moderate Evidence).","entity_name":"ZBTB42","entity_type":"gene"},{"created":"2021-11-22T21:17:25.789523+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.669","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UNC50 as ready","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:17:25.778777+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.669","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc50 has been classified as Amber List (Moderate Evidence).","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:17:22.289929+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.669","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC50 were changed from  to Arthrogryposis multiplex congenita","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:17:09.370936+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.668","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UNC50 as Amber List (moderate evidence)","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:17:09.358807+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.668","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc50 has been classified as Amber List (Moderate Evidence).","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:16:57.700982+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.667","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: UNC50: Added comment: Supportive functional data.; Changed rating: AMBER","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:16:14.819901+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.667","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UNC50: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"UNC50","entity_type":"gene"},{"created":"2021-11-22T21:15:45.357350+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.667","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOR1AIP1 as ready","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:15:45.347299+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.667","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1aip1 has been classified as Green List (High Evidence).","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:15:42.066497+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.667","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TOR1AIP1 were changed from ?Muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures - #61707; congenital myasthenic syndrome to Muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures - #61707; congenital myasthenic syndrome","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:15:29.595324+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.666","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOR1AIP1 as Green List (high evidence)","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:15:29.585241+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.666","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1aip1 has been classified as Green List (High Evidence).","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:15:15.175019+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.665","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TOR1AIP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2021-11-22T21:14:23.884215+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.665","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STIM1 as ready","entity_name":"STIM1","entity_type":"gene"},{"created":"2021-11-22T21:14:23.873571+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.665","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stim1 has been classified as Green List (High Evidence).","entity_name":"STIM1","entity_type":"gene"},{"created":"2021-11-22T21:14:18.785739+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.665","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: STIM1 as Green List (high evidence)","entity_name":"STIM1","entity_type":"gene"},{"created":"2021-11-22T21:14:18.776635+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.665","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stim1 has been classified as Green List (High Evidence).","entity_name":"STIM1","entity_type":"gene"},{"created":"2021-11-22T21:13:23.768697+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.664","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SCYL2 as ready","entity_name":"SCYL2","entity_type":"gene"},{"created":"2021-11-22T21:13:23.757828+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.664","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: scyl2 has been classified as Amber List (Moderate Evidence).","entity_name":"SCYL2","entity_type":"gene"},{"created":"2021-11-22T21:13:18.389307+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.664","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SCYL2 as Amber List (moderate evidence)","entity_name":"SCYL2","entity_type":"gene"},{"created":"2021-11-22T21:13:18.370865+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.664","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: scyl2 has been classified as Amber List (Moderate Evidence).","entity_name":"SCYL2","entity_type":"gene"},{"created":"2021-11-22T20:11:40.711225+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.663","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIP5K1C as ready","entity_name":"PIP5K1C","entity_type":"gene"},{"created":"2021-11-22T20:11:40.699772+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pip5k1c has been classified as Amber List (Moderate Evidence).","entity_name":"PIP5K1C","entity_type":"gene"},{"created":"2021-11-22T20:11:19.726847+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.663","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIP5K1C as Amber List (moderate evidence)","entity_name":"PIP5K1C","entity_type":"gene"},{"created":"2021-11-22T20:11:19.700607+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pip5k1c has been classified as Amber List (Moderate Evidence).","entity_name":"PIP5K1C","entity_type":"gene"},{"created":"2021-11-22T20:10:44.964244+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.662","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ORAI1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ORAI1","entity_type":"gene"},{"created":"2021-11-22T20:09:51.226790+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.662","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ORAI1 as ready","entity_name":"ORAI1","entity_type":"gene"},{"created":"2021-11-22T20:09:51.212215+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orai1 has been classified as Green List (High Evidence).","entity_name":"ORAI1","entity_type":"gene"},{"created":"2021-11-22T20:09:39.588569+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.662","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ORAI1 as Green List (high evidence)","entity_name":"ORAI1","entity_type":"gene"},{"created":"2021-11-22T20:09:39.577717+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orai1 has been classified as Green List (High Evidence).","entity_name":"ORAI1","entity_type":"gene"},{"created":"2021-11-22T20:08:50.792031+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.661","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYLPF as ready","entity_name":"MYLPF","entity_type":"gene"},{"created":"2021-11-22T20:08:50.776106+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.661","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mylpf has been classified as Amber List (Moderate Evidence).","entity_name":"MYLPF","entity_type":"gene"},{"created":"2021-11-22T20:08:41.750111+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.661","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYLPF as Amber List (moderate evidence)","entity_name":"MYLPF","entity_type":"gene"},{"created":"2021-11-22T20:08:41.739598+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.661","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mylpf has been classified as Amber List (Moderate Evidence).","entity_name":"MYLPF","entity_type":"gene"},{"created":"2021-11-22T20:08:28.958475+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.660","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYLPF: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MYLPF","entity_type":"gene"},{"created":"2021-11-22T20:07:06.670043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9840","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF6 as ready","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:07:06.659010+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9840","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf6 has been classified as Green List (High Evidence).","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:06:58.723451+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9840","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRF6 were changed from Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300 to Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:06:40.265449+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9839","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRF6 were set to 20301581","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:06:25.091103+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9838","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF6 as ready","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:06:25.080831+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9838","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf6 has been classified as Green List (High Evidence).","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:06:16.916488+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9838","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRF6 were changed from  to Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:05:57.463301+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9837","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRF6 were set to ","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:05:30.528610+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9836","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IRF6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IRF6","entity_type":"gene"},{"created":"2021-11-22T20:04:21.029160+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9835","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MATN3 as ready","entity_name":"MATN3","entity_type":"gene"},{"created":"2021-11-22T20:04:21.017893+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9835","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: matn3 has been classified as Green List (High Evidence).","entity_name":"MATN3","entity_type":"gene"},{"created":"2021-11-22T20:04:13.226737+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9835","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MATN3 were changed from  to Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type (MIM#608728); Epiphyseal dysplasia, multiple, 5 (MIM#607078)","entity_name":"MATN3","entity_type":"gene"},{"created":"2021-11-22T20:03:49.808271+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9834","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MATN3 were set to ","entity_name":"MATN3","entity_type":"gene"},{"created":"2021-11-22T20:02:11.639736+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9833","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MATN3 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MATN3","entity_type":"gene"},{"created":"2021-11-22T20:01:02.273775+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9832","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INPPL1 as ready","entity_name":"INPPL1","entity_type":"gene"},{"created":"2021-11-22T20:01:02.243075+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9832","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: inppl1 has been classified as Green List (High Evidence).","entity_name":"INPPL1","entity_type":"gene"},{"created":"2021-11-22T18:45:03.546898+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9832","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INPPL1 were changed from  to Opsismodysplasia MIM#258480","entity_name":"INPPL1","entity_type":"gene"},{"created":"2021-11-22T18:44:41.984163+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9831","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INPPL1 were set to ","entity_name":"INPPL1","entity_type":"gene"},{"created":"2021-11-22T18:44:23.097362+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9830","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INPPL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"INPPL1","entity_type":"gene"},{"created":"2021-11-22T18:43:54.400976+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9829","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INPPL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"INPPL1","entity_type":"gene"}]}