{"count":220313,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1438","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1436","results":[{"created":"2021-01-20T16:26:21.856114+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.33","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: stk11 has been classified as Amber List (Moderate Evidence).","entity_name":"STK11","entity_type":"gene"},{"created":"2021-01-20T16:25:53.517055+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.32","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: STK11: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"STK11","entity_type":"gene"},{"created":"2021-01-20T16:24:56.528582+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.32","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: SUFU as Red List (low evidence)","entity_name":"SUFU","entity_type":"gene"},{"created":"2021-01-20T16:24:56.522450+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.32","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"SUFU","entity_type":"gene"},{"created":"2021-01-20T16:24:56.498150+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.32","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: sufu has been classified as Red List (Low Evidence).","entity_name":"SUFU","entity_type":"gene"},{"created":"2021-01-20T16:24:45.178275+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.31","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: SUFU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SUFU","entity_type":"gene"},{"created":"2021-01-20T16:23:50.979982+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.31","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TACC1 as Red List (low evidence)","entity_name":"TACC1","entity_type":"gene"},{"created":"2021-01-20T16:23:50.972170+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.31","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tacc1 has been classified as Red List (Low Evidence).","entity_name":"TACC1","entity_type":"gene"},{"created":"2021-01-20T16:23:41.246422+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.30","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TACC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TACC1","entity_type":"gene"},{"created":"2021-01-20T16:23:17.724005+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.30","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TACC3 as Red List (low evidence)","entity_name":"TACC3","entity_type":"gene"},{"created":"2021-01-20T16:23:17.718881+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.30","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: not a clear cause of Mendelian disease","entity_name":"TACC3","entity_type":"gene"},{"created":"2021-01-20T16:23:17.694549+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.30","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tacc3 has been classified as Red List (Low Evidence).","entity_name":"TACC3","entity_type":"gene"},{"created":"2021-01-20T16:23:06.061305+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.29","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TACC3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TACC3","entity_type":"gene"},{"created":"2021-01-20T16:22:26.373898+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.29","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TAF15 as Red List (low evidence)","entity_name":"TAF15","entity_type":"gene"},{"created":"2021-01-20T16:22:26.368858+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.29","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: not clearly a cause of germline inherited disease","entity_name":"TAF15","entity_type":"gene"},{"created":"2021-01-20T16:22:26.329327+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.29","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: taf15 has been classified as Red List (Low Evidence).","entity_name":"TAF15","entity_type":"gene"},{"created":"2021-01-20T16:21:03.787380+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Marked gene: TARDBP as ready","entity_name":"TARDBP","entity_type":"gene"},{"created":"2021-01-20T16:21:03.784118+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment when marking as ready: Adult onset neurological condition - should be kept on this list","entity_name":"TARDBP","entity_type":"gene"},{"created":"2021-01-20T16:21:03.759182+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tardbp has been classified as Green List (High Evidence).","entity_name":"TARDBP","entity_type":"gene"},{"created":"2021-01-20T16:19:58.464256+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Marked gene: TBL1XR1 as ready","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-01-20T16:19:58.452706+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tbl1xr1 has been classified as Red List (Low Evidence).","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-01-20T16:19:54.515687+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TBL1XR1 as Red List (low evidence)","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-01-20T16:19:54.511723+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-01-20T16:19:54.481932+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.28","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tbl1xr1 has been classified as Red List (Low Evidence).","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-01-20T16:19:10.630308+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.27","user_name":"Tony Roscioli","item_type":"entity","text":"Marked gene: TFG as ready","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:19:10.625590+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.27","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment when marking as ready: may present in childhood","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:19:10.601775+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.27","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tfg has been classified as Red List (Low Evidence).","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:19:03.635800+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.27","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TFG as Red List (low evidence)","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:19:03.628081+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.27","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tfg has been classified as Red List (Low Evidence).","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:18:53.046704+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.26","user_name":"Tony Roscioli","item_type":"entity","text":"edited their review of gene: TFG: Added comment: may present in childhood; Changed rating: RED","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:18:30.054579+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.26","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TGFBR1 as Red List (low evidence)","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2021-01-20T16:18:30.049551+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.26","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2021-01-20T16:18:30.019968+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.26","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tgfbr1 has been classified as Red List (Low Evidence).","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2021-01-20T16:17:59.319782+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.25","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TGFBR2 as Red List (low evidence)","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-01-20T16:17:59.314952+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.25","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-01-20T16:17:59.289041+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.25","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tgfbr2 has been classified as Red List (Low Evidence).","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-01-20T16:17:44.919131+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.24","user_name":"Tony Roscioli","item_type":"entity","text":"edited their review of gene: TGFBR2: Added comment: may present in childhood; Changed rating: RED","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-01-20T16:17:09.739546+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.24","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TNNI3 as Red List (low evidence)","entity_name":"TNNI3","entity_type":"gene"},{"created":"2021-01-20T16:17:09.736381+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.24","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: Disease has been observed in childhood","entity_name":"TNNI3","entity_type":"gene"},{"created":"2021-01-20T16:17:09.719267+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.24","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tnni3 has been classified as Red List (Low Evidence).","entity_name":"TNNI3","entity_type":"gene"},{"created":"2021-01-20T16:15:59.856937+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.23","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TNNT2 as Red List (low evidence)","entity_name":"TNNT2","entity_type":"gene"},{"created":"2021-01-20T16:15:59.853421+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.23","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"TNNT2","entity_type":"gene"},{"created":"2021-01-20T16:15:59.834839+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.23","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tnnt2 has been classified as Red List (Low Evidence).","entity_name":"TNNT2","entity_type":"gene"},{"created":"2021-01-20T16:14:53.759026+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.22","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TREM2 as Amber List (moderate evidence)","entity_name":"TREM2","entity_type":"gene"},{"created":"2021-01-20T16:14:53.755817+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.22","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: Neurological symptoms appear not to present in childhood - needs review for a final decision","entity_name":"TREM2","entity_type":"gene"},{"created":"2021-01-20T16:14:53.737472+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.22","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: trem2 has been classified as Amber List (Moderate Evidence).","entity_name":"TREM2","entity_type":"gene"},{"created":"2021-01-20T16:12:33.479945+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.21","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TET2 as Red List (low evidence)","entity_name":"TET2","entity_type":"gene"},{"created":"2021-01-20T16:12:33.475388+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.21","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: may present in childhood","entity_name":"TET2","entity_type":"gene"},{"created":"2021-01-20T16:12:33.450951+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.21","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tet2 has been classified as Red List (Low Evidence).","entity_name":"TET2","entity_type":"gene"},{"created":"2021-01-20T16:11:51.384031+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.20","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TCF12 as Red List (low evidence)","entity_name":"TCF12","entity_type":"gene"},{"created":"2021-01-20T16:11:51.371532+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.20","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tcf12 has been classified as Red List (Low Evidence).","entity_name":"TCF12","entity_type":"gene"},{"created":"2021-01-20T16:11:49.956984+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6101","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: ZMYND15 as ready","entity_name":"ZMYND15","entity_type":"gene"},{"created":"2021-01-20T16:11:49.949492+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6101","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: zmynd15 has been classified as Green List (High Evidence).","entity_name":"ZMYND15","entity_type":"gene"},{"created":"2021-01-20T16:11:33.651949+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TCF12: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TCF12","entity_type":"gene"},{"created":"2021-01-20T16:10:49.773512+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TET2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TET2","entity_type":"gene"},{"created":"2021-01-20T16:09:00.676823+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TFG: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TFG","entity_type":"gene"},{"created":"2021-01-20T16:08:19.044441+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TGFBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2021-01-20T16:07:46.562534+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TGFBR2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-01-20T16:06:46.426434+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TMEM43 as Amber List (moderate evidence)","entity_name":"TMEM43","entity_type":"gene"},{"created":"2021-01-20T16:06:46.419306+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: unclear whether disease presents in childhood - needs review","entity_name":"TMEM43","entity_type":"gene"},{"created":"2021-01-20T16:06:46.378767+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.19","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tmem43 has been classified as Amber List (Moderate Evidence).","entity_name":"TMEM43","entity_type":"gene"},{"created":"2021-01-20T16:05:15.256591+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6101","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: ZMYND15 as Green List (high evidence)","entity_name":"ZMYND15","entity_type":"gene"},{"created":"2021-01-20T16:05:15.248330+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6101","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: zmynd15 has been classified as Green List (High Evidence).","entity_name":"ZMYND15","entity_type":"gene"},{"created":"2021-01-20T16:04:53.863347+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.18","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TNNI3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TNNI3","entity_type":"gene"},{"created":"2021-01-20T16:04:43.775886+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6100","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ZMYND15 was added\ngene: ZMYND15 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: ZMYND15 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZMYND15 were set to 24431330; 33169450; 20675388\nPhenotypes for gene: ZMYND15 were set to Severe oligozoospermia\nReview for gene: ZMYND15 was set to GREEN\nAdded comment: 4 unrelated consanguineous cases with homozygous loss of function variants. Zmynd15-null male mice display reduced testis weight and azoospermia \nSources: Literature","entity_name":"ZMYND15","entity_type":"gene"},{"created":"2021-01-20T16:04:07.413996+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.18","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TNNT2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TNNT2","entity_type":"gene"},{"created":"2021-01-20T15:47:49.321742+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.18","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TP53 as Amber List (moderate evidence)","entity_name":"TP53","entity_type":"gene"},{"created":"2021-01-20T15:47:49.317065+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.18","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: Needs discussion - could be removed as early age of onset possible","entity_name":"TP53","entity_type":"gene"},{"created":"2021-01-20T15:47:49.279953+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.18","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tp53 has been classified as Amber List (Moderate Evidence).","entity_name":"TP53","entity_type":"gene"},{"created":"2021-01-20T15:46:36.382475+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.17","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TPM1 as Amber List (moderate evidence)","entity_name":"TPM1","entity_type":"gene"},{"created":"2021-01-20T15:46:36.378610+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.17","user_name":"Tony Roscioli","item_type":"entity","text":"Added comment: Comment on list classification: May cause a treatable cardiomyopathy - should be reviewed for exclusion","entity_name":"TPM1","entity_type":"gene"},{"created":"2021-01-20T15:46:36.349907+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.17","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tpm1 has been classified as Amber List (Moderate Evidence).","entity_name":"TPM1","entity_type":"gene"},{"created":"2021-01-20T15:44:38.070404+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.16","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TPR as Red List (low evidence)","entity_name":"TPR","entity_type":"gene"},{"created":"2021-01-20T15:44:38.061941+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.16","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: tpr has been classified as Red List (Low Evidence).","entity_name":"TPR","entity_type":"gene"},{"created":"2021-01-20T15:44:07.392933+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.15","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TPR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TPR","entity_type":"gene"},{"created":"2021-01-20T15:42:11.140706+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.15","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TREM2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TREM2","entity_type":"gene"},{"created":"2021-01-20T15:40:19.512206+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.15","user_name":"Tony Roscioli","item_type":"entity","text":"Classified gene: TRIM24 as Red List (low evidence)","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T15:40:19.500343+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.15","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: trim24 has been classified as Red List (Low Evidence).","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T15:39:56.091262+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.14","user_name":"Tony Roscioli","item_type":"entity","text":"Marked gene: TRIM24 as ready","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T15:39:56.078915+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.14","user_name":"Tony Roscioli","item_type":"entity","text":"Gene: trim24 has been classified as Green List (High Evidence).","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T15:39:07.877786+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.14","user_name":"Tony Roscioli","item_type":"entity","text":"changed review comment from: Not a known Mendelian disease gene; to: Not a known Mendelian disease gene","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T15:36:34.641916+11:00","panel_name":"Incidentalome_PREGEN_DRAFT","panel_id":3437,"panel_version":"0.14","user_name":"Tony Roscioli","item_type":"entity","text":"reviewed gene: TRIM24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TRIM24","entity_type":"gene"},{"created":"2021-01-20T11:52:17.133728+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-01-20T11:51:14.672915+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6099","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNPLA1 as ready","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:51:14.662738+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6099","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnpla1 has been classified as Green List (High Evidence).","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:51:04.591828+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6099","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PNPLA1 were changed from  to Ichthyosis, congenital, autosomal recessive 10, MIM# 615024","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:50:41.408857+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6098","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PNPLA1 were set to ","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:50:19.772340+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6097","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PNPLA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:50:01.951292+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6096","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PNPLA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22246504, 24344921, 26691440; Phenotypes: Ichthyosis, congenital, autosomal recessive 10, MIM# 615024; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:49:11.957119+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNPLA1 as ready","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:49:11.949932+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnpla1 has been classified as Green List (High Evidence).","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:49:08.967228+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PNPLA1 were changed from  to Ichthyosis, congenital, autosomal recessive 10, MIM# 615024","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:48:36.456562+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PNPLA1 were set to ","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:48:07.059948+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PNPLA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:47:38.079190+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PNPLA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22246504, 24344921, 26691440; Phenotypes: Ichthyosis, congenital, autosomal recessive 10, MIM# 615024; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA1","entity_type":"gene"},{"created":"2021-01-20T11:45:43.444103+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: STS: Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"STS","entity_type":"gene"},{"created":"2021-01-20T11:45:35.428381+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STS as ready","entity_name":"STS","entity_type":"gene"},{"created":"2021-01-20T11:45:35.420042+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sts has been classified as Green List (High Evidence).","entity_name":"STS","entity_type":"gene"},{"created":"2021-01-20T11:45:32.725713+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STS were changed from  to Ichthyosis, X-linked, MIM# 308100","entity_name":"STS","entity_type":"gene"},{"created":"2021-01-20T11:45:03.042940+11:00","panel_name":"Ichthyosis","panel_id":124,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STS was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"STS","entity_type":"gene"}]}