{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2104","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2102","results":[{"created":"2019-11-20T21:13:38.919605+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryl1 has been classified as Red List (Low Evidence).","entity_name":"CRYL1","entity_type":"gene"},{"created":"2019-11-20T21:13:24.634031+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CRYL1 as Red List (low evidence)","entity_name":"CRYL1","entity_type":"gene"},{"created":"2019-11-20T21:13:24.614868+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cryl1 has been classified as Red List (Low Evidence).","entity_name":"CRYL1","entity_type":"gene"},{"created":"2019-11-20T21:13:01.654529+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYL1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"CRYL1","entity_type":"gene"},{"created":"2019-11-20T21:11:23.595742+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQCG as ready","entity_name":"IQCG","entity_type":"gene"},{"created":"2019-11-20T21:11:23.584634+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqcg has been classified as Red List (Low Evidence).","entity_name":"IQCG","entity_type":"gene"},{"created":"2019-11-20T21:11:13.028108+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IQCG as Red List (low evidence)","entity_name":"IQCG","entity_type":"gene"},{"created":"2019-11-20T21:11:13.016436+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqcg has been classified as Red List (Low Evidence).","entity_name":"IQCG","entity_type":"gene"},{"created":"2019-11-20T21:10:52.016381+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IQCG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"IQCG","entity_type":"gene"},{"created":"2019-11-20T16:39:16.877451+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_VCGS","panel_id":211,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: VTN: Added comment: Over-representation in cases vs controls but no functional data and mechanism unclear at present.; Changed phenotypes: Atypical haemolytic uraemic syndrome","entity_name":"VTN","entity_type":"gene"},{"created":"2019-11-20T15:53:11.975252+11:00","panel_name":"Renal cystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Renal cystic disease_KidGen to Renal cystic disease_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-20T15:51:23.544159+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DZIP1L as ready","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-20T15:51:23.533008+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dzip1l has been classified as Green List (High Evidence).","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-20T15:51:17.464917+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DZIP1L as Green List (high evidence)","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-20T15:51:17.453610+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dzip1l has been classified as Green List (High Evidence).","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-20T15:51:00.215919+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DZIP1L was added\ngene: DZIP1L was added to Renal cystic disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DZIP1L was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DZIP1L were set to 28530676\nPhenotypes for gene: DZIP1L were set to Polycystic kidney disease 5, MIM#617610\nReview for gene: DZIP1L was set to GREEN\ngene: DZIP1L was marked as current diagnostic\nAdded comment: 7 individuals from 4 unrelated families with bi-allelic variants in this gene. \nSources: Expert list","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-20T15:48:32.970095+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJB11 as ready","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:48:32.958869+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajb11 has been classified as Green List (High Evidence).","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:48:27.784269+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJB11 as Green List (high evidence)","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:48:27.772905+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajb11 has been classified as Green List (High Evidence).","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:48:15.507165+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJB11 was added\ngene: DNAJB11 was added to Renal cystic disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DNAJB11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DNAJB11 were set to 29706351; 29777155\nPhenotypes for gene: DNAJB11 were set to Polycystic kidney disease 6 with or without polycystic liver disease, MIM#618061\nReview for gene: DNAJB11 was set to GREEN\ngene: DNAJB11 was marked as current diagnostic\nAdded comment: Seven families described with phenotypes overlapping ADTKD and ADPKD. \nSources: Expert list","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:46:01.313628+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALMS1 as ready","entity_name":"ALMS1","entity_type":"gene"},{"created":"2019-11-20T15:46:01.301979+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alms1 has been classified as Red List (Low Evidence).","entity_name":"ALMS1","entity_type":"gene"},{"created":"2019-11-20T15:45:57.912589+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ALMS1 as Red List (low evidence)","entity_name":"ALMS1","entity_type":"gene"},{"created":"2019-11-20T15:45:57.900760+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alms1 has been classified as Red List (Low Evidence).","entity_name":"ALMS1","entity_type":"gene"},{"created":"2019-11-20T15:45:43.055841+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALMS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ALMS1","entity_type":"gene"},{"created":"2019-11-20T15:45:22.145448+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTN4 as ready","entity_name":"ACTN4","entity_type":"gene"},{"created":"2019-11-20T15:45:22.134247+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actn4 has been classified as Red List (Low Evidence).","entity_name":"ACTN4","entity_type":"gene"},{"created":"2019-11-20T15:45:18.315175+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACTN4 as Red List (low evidence)","entity_name":"ACTN4","entity_type":"gene"},{"created":"2019-11-20T15:45:18.303699+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actn4 has been classified as Red List (Low Evidence).","entity_name":"ACTN4","entity_type":"gene"},{"created":"2019-11-20T15:45:05.984854+11:00","panel_name":"Renal cystic disease_KidGen","panel_id":194,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACTN4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ACTN4","entity_type":"gene"},{"created":"2019-11-20T15:39:48.777811+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS","panel_id":211,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Atypical Haemolytic Uraemic Syndrome_VCGS to Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-20T15:38:45.313595+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_VCGS","panel_id":211,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VTN as ready","entity_name":"VTN","entity_type":"gene"},{"created":"2019-11-20T15:38:45.302153+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_VCGS","panel_id":211,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vtn has been classified as Amber List (Moderate Evidence).","entity_name":"VTN","entity_type":"gene"},{"created":"2019-11-20T15:38:35.464348+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_VCGS","panel_id":211,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VTN as Amber List (moderate evidence)","entity_name":"VTN","entity_type":"gene"},{"created":"2019-11-20T15:38:35.442740+11:00","panel_name":"Atypical Haemolytic Uraemic Syndrome_VCGS","panel_id":211,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vtn has been classified as Amber List (Moderate Evidence).","entity_name":"VTN","entity_type":"gene"},{"created":"2019-11-20T15:30:58.388229+11:00","panel_name":"Renal tubulointerstitial disease_KidGen_VCGS","panel_id":199,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Renal tubulointerstitial disease_KidGen to Renal tubulointerstitial disease_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-20T15:27:13.377590+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJB11 as ready","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:27:13.366456+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajb11 has been classified as Green List (High Evidence).","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:27:08.666350+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJB11 as Green List (high evidence)","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:27:08.655474+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajb11 has been classified as Green List (High Evidence).","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:26:51.276537+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJB11 was added\ngene: DNAJB11 was added to Renal tubulointerstitial disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DNAJB11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DNAJB11 were set to 29706351; 29777155\nPhenotypes for gene: DNAJB11 were set to Polycystic kidney disease 6 with or without polycystic liver disease, MIM#618061\nReview for gene: DNAJB11 was set to GREEN\ngene: DNAJB11 was marked as current diagnostic\nAdded comment: At least 7 unrelated families with variants reported in this gene; variable presentation including tubulointerstitial disease (histologically) in addition to polycystic disease (hybrid between PKD and ADTKD). \nSources: Expert list","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-20T15:22:06.225190+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP6V0A4 as ready","entity_name":"ATP6V0A4","entity_type":"gene"},{"created":"2019-11-20T15:22:06.213589+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp6v0a4 has been classified as Red List (Low Evidence).","entity_name":"ATP6V0A4","entity_type":"gene"},{"created":"2019-11-20T15:22:01.191214+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATP6V0A4 as Red List (low evidence)","entity_name":"ATP6V0A4","entity_type":"gene"},{"created":"2019-11-20T15:22:01.179488+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp6v0a4 has been classified as Red List (Low Evidence).","entity_name":"ATP6V0A4","entity_type":"gene"},{"created":"2019-11-20T15:21:50.885678+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATP6V0A4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal tubular acidosis, distal, autosomal recessive, MIM#602722; Mode of inheritance: None","entity_name":"ATP6V0A4","entity_type":"gene"},{"created":"2019-11-20T15:20:11.285683+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AQP2 as ready","entity_name":"AQP2","entity_type":"gene"},{"created":"2019-11-20T15:20:11.274276+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aqp2 has been classified as Red List (Low Evidence).","entity_name":"AQP2","entity_type":"gene"},{"created":"2019-11-20T15:20:08.010763+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AQP2 as Red List (low evidence)","entity_name":"AQP2","entity_type":"gene"},{"created":"2019-11-20T15:20:07.997891+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aqp2 has been classified as Red List (Low Evidence).","entity_name":"AQP2","entity_type":"gene"},{"created":"2019-11-20T15:19:51.212843+11:00","panel_name":"Renal tubulointerstitial disease_KidGen","panel_id":199,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AQP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Diabetes insipidus, nephrogenic, MIM#125800; Mode of inheritance: None","entity_name":"AQP2","entity_type":"gene"},{"created":"2019-11-20T15:01:03.944706+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FBF1 as ready","entity_name":"FBF1","entity_type":"gene"},{"created":"2019-11-20T15:01:03.933498+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbf1 has been classified as Red List (Low Evidence).","entity_name":"FBF1","entity_type":"gene"},{"created":"2019-11-20T15:00:55.363971+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FBF1 as Red List (low evidence)","entity_name":"FBF1","entity_type":"gene"},{"created":"2019-11-20T15:00:55.351893+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fbf1 has been classified as Red List (Low Evidence).","entity_name":"FBF1","entity_type":"gene"},{"created":"2019-11-20T15:00:12.569545+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FBF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"FBF1","entity_type":"gene"},{"created":"2019-11-20T14:56:14.969750+11:00","panel_name":"Overgrowth_VCGS","panel_id":151,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF135 as ready","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:56:14.958724+11:00","panel_name":"Overgrowth_VCGS","panel_id":151,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:56:10.499493+11:00","panel_name":"Overgrowth_VCGS","panel_id":151,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF135 as Red List (low evidence)","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:56:10.487989+11:00","panel_name":"Overgrowth_VCGS","panel_id":151,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:55:24.552643+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF135 as ready","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:55:24.541562+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:55:16.213637+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF135 as Red List (low evidence)","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:55:16.202381+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:54:43.240267+11:00","panel_name":"Macrocephaly/Megalencephaly_VCGS","panel_id":135,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF135 as ready","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:54:43.228614+11:00","panel_name":"Macrocephaly/Megalencephaly_VCGS","panel_id":135,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:54:35.883889+11:00","panel_name":"Macrocephaly/Megalencephaly_VCGS","panel_id":135,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF135 as Red List (low evidence)","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:54:35.872416+11:00","panel_name":"Macrocephaly/Megalencephaly_VCGS","panel_id":135,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:53:50.276195+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF135 as ready","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:53:50.265104+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:53:46.289980+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF135 as Red List (low evidence)","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:53:46.276847+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf135 has been classified as Red List (Low Evidence).","entity_name":"RNF135","entity_type":"gene"},{"created":"2019-11-20T14:42:12.191006+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC1 as ready","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:42:12.179505+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:42:03.611638+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LAMC1 as Red List (low evidence)","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:42:03.600575+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:41:44.263582+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:41:08.298988+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC1 as ready","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:41:08.287815+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:41:03.851042+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LAMC1 as Red List (low evidence)","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:41:03.839437+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:40:28.671517+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:39:49.705563+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC1 as ready","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:39:49.694384+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:39:43.622635+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LAMC1 as Red List (low evidence)","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:39:43.605557+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc1 has been classified as Red List (Low Evidence).","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:39:14.036444+11:00","panel_name":"Joubert syndrome and other cerebellar malformations_VCGS","panel_id":129,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"LAMC1","entity_type":"gene"},{"created":"2019-11-20T14:35:55.463110+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCN2 as ready","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:35:55.450932+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn2 has been classified as Amber List (Moderate Evidence).","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:35:44.749220+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HCN2 as Amber List (moderate evidence)","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:35:44.736894+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn2 has been classified as Amber List (Moderate Evidence).","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:33:11.368247+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCN2 as ready","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:33:11.357038+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn2 has been classified as Amber List (Moderate Evidence).","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:33:05.737008+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HCN2 as Amber List (moderate evidence)","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:33:05.725154+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn2 has been classified as Amber List (Moderate Evidence).","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:32:36.751531+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HCN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 22131395, 30986657; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HCN2","entity_type":"gene"},{"created":"2019-11-20T14:24:57.175462+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B3GNT2 as ready","entity_name":"B3GNT2","entity_type":"gene"},{"created":"2019-11-20T14:24:57.164181+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3gnt2 has been classified as Red List (Low Evidence).","entity_name":"B3GNT2","entity_type":"gene"},{"created":"2019-11-20T14:24:53.129830+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B3GNT2 as Red List (low evidence)","entity_name":"B3GNT2","entity_type":"gene"}]}