{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1442","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1440","results":[{"created":"2021-01-17T10:51:34.360985+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: KCNA1 was changed from  to Other","entity_name":"KCNA1","entity_type":"gene"},{"created":"2021-01-17T10:51:27.589779+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KCNA1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KCNA1","entity_type":"gene"},{"created":"2021-01-17T10:50:52.644624+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6070","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLCN1 as ready","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:50:52.635431+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6070","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn1 has been classified as Green List (High Evidence).","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:50:44.992170+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6070","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLCN1 were changed from  to Myotonia congenita, dominant 160800; Myotonia congenita, recessive 255700","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:50:27.416961+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6069","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLCN1 were set to ","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:50:07.913564+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6068","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLCN1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:49:07.684717+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6067","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLCN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 1379744, 7981750, 8533761; Phenotypes: Myotonia congenita, dominant 160800, Myotonia congenita, recessive 255700; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:47:51.888593+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLCN1 as ready","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:47:51.877464+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn1 has been classified as Green List (High Evidence).","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:47:45.596742+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLCN1 were set to ","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:47:32.661129+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLCN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 1379744, 7981750, 8533761; Phenotypes: Myotonia congenita, dominant 160800, Myotonia congenita, recessive 255700; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CLCN1","entity_type":"gene"},{"created":"2021-01-17T10:45:14.743022+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CACNA1S as ready","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2021-01-17T10:45:14.733065+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1s has been classified as Green List (High Evidence).","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2021-01-17T10:45:11.191384+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CACNA1S were set to ","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2021-01-17T10:44:57.939461+11:00","panel_name":"Skeletal Muscle Channelopathies","panel_id":302,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CACNA1S: Rating: GREEN; Mode of pathogenicity: None; Publications: 8004673, 11591859; Phenotypes: Hypokalemic periodic paralysis, type 1, MIM# 170400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2021-01-17T10:41:09.011084+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"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":"2021-01-17T10:35:05.344833+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL9A2 as ready","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:35:05.334667+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col9a2 has been classified as Green List (High Evidence).","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:35:03.298406+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL9A2 were changed from  to Stickler syndrome, type V, MIM# 614284","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:34:53.861448+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL9A2 were set to ","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:34:44.285532+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL9A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:34:30.604299+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL9A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 21671392, 31090205, 33356723; Phenotypes: Stickler syndrome, type V, MIM# 614284; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL9A2","entity_type":"gene"},{"created":"2021-01-17T10:27:50.401709+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL9A1 as ready","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:27:50.393536+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col9a1 has been classified as Green List (High Evidence).","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:27:48.329942+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL9A1 were changed from  to Stickler syndrome, type IV, MIM# 614134","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:27:37.461536+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL9A1 were set to ","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:27:25.098956+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL9A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:27:13.783148+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL9A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 16909383, 21421862, 31090205; Phenotypes: Stickler syndrome, type IV, MIM# 614134; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL9A1","entity_type":"gene"},{"created":"2021-01-17T10:25:15.327293+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL2A1 as ready","entity_name":"COL2A1","entity_type":"gene"},{"created":"2021-01-17T10:25:15.315201+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col2a1 has been classified as Green List (High Evidence).","entity_name":"COL2A1","entity_type":"gene"},{"created":"2021-01-17T10:25:09.208221+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL2A1 were changed from  to Stickler syndrome, type I, MIM# 108300","entity_name":"COL2A1","entity_type":"gene"},{"created":"2021-01-17T10:24:59.958480+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL2A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL2A1","entity_type":"gene"},{"created":"2021-01-17T10:24:48.963120+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Stickler syndrome, type I, MIM# 108300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL2A1","entity_type":"gene"},{"created":"2021-01-17T10:24:06.415255+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL11A2 as ready","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:24:06.406731+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col11a2 has been classified as Green List (High Evidence).","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:24:03.804049+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL11A2 were changed from  to Stickler syndrome type 3","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:23:55.504999+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL11A2 were set to ","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:23:41.957192+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL11A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:23:31.992460+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL11A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 25240749, 22796475, 20112039; Phenotypes: Stickler syndrome type 3; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL11A2","entity_type":"gene"},{"created":"2021-01-17T10:18:25.933214+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL11A1 as ready","entity_name":"COL11A1","entity_type":"gene"},{"created":"2021-01-17T10:18:25.922888+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col11a1 has been classified as Green List (High Evidence).","entity_name":"COL11A1","entity_type":"gene"},{"created":"2021-01-17T10:18:22.926507+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL11A1 were changed from  to Stickler syndrome, type II, MIM# 604841, MONDO:0011493","entity_name":"COL11A1","entity_type":"gene"},{"created":"2021-01-17T10:18:04.642231+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL11A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL11A1","entity_type":"gene"},{"created":"2021-01-17T10:17:53.455264+11:00","panel_name":"Stickler Syndrome","panel_id":3114,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL11A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Stickler syndrome, type II, MIM# 604841, MONDO:0011493; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL11A1","entity_type":"gene"},{"created":"2021-01-16T22:32:11.420075+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"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":"2021-01-16T22:31:42.371941+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UMOD as ready","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:31:42.360145+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: umod has been classified as Green List (High Evidence).","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:31:38.877354+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UMOD were changed from  to Autosomal Dominant Tubulointerstitial disease (ADTKD-UMOD); Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886; Medullary cystic kidney disease 2, MIM# 603860","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:31:09.479033+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UMOD were set to ","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:30:34.062487+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UMOD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:30:02.024837+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UMOD: Rating: GREEN; Mode of pathogenicity: None; Publications: 32954071, 32847529, 32450155; Phenotypes: Autosomal Dominant Tubulointerstitial disease (ADTKD-UMOD), Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886, Medullary cystic kidney disease 2, MIM# 603860; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UMOD","entity_type":"gene"},{"created":"2021-01-16T22:19:59.907043+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTOR as ready","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:19:59.898211+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtor has been classified as Green List (High Evidence).","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:19:56.379005+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTOR were changed from  to Smith-Kingsmore syndrome, MIM# 616638","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:19:29.538799+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTOR were set to ","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:18:26.307270+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MTOR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:17:56.845767+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MTOR: Rating: GREEN; Mode of pathogenicity: None; Publications: 28892148; Phenotypes: Smith-Kingsmore syndrome, MIM# 616638; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-01-16T22:14:15.993920+11:00","panel_name":"Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly to Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly","entity_name":null,"entity_type":null},{"created":"2021-01-16T22:13:26.070632+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AKT3 as ready","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:13:26.061873+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Green List (High Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:13:22.274099+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AKT3 were changed from  to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:11:28.259617+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: AKT3 was changed from  to Other","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:11:03.912939+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AKT3 were set to ","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:10:30.416759+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AKT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:09:58.870903+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AKT3: Rating: GREEN; Mode of pathogenicity: Other; Publications: 22729224, 22729223, 32446860, 31441589; Phenotypes: Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-01-16T22:06:04.257691+11:00","panel_name":"Tuberous Sclerosis_Cortical Dysplasia_Hemimegalencephaly","panel_id":20,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Australian Genomics; Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2021-01-16T22:02:46.596420+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6067","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBG1 as ready","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:02:46.586202+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6067","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubg1 has been classified as Green List (High Evidence).","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:02:34.797070+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6067","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBG1 were changed from  to Cortical dysplasia, complex, with other brain malformations 4, MIM# 615412","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:02:10.032031+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6066","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBG1 were set to ","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:01:45.816246+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6065","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:01:27.480760+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6064","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 31086189; Phenotypes: Cortical dysplasia, complex, with other brain malformations 4, MIM# 615412; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T22:00:12.682298+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6064","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB3 as ready","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T22:00:12.672119+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6064","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb3 has been classified as Green List (High Evidence).","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T22:00:01.393629+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6064","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB3 were changed from  to Cortical dysplasia, complex, with other brain malformations 1, MIM# 614039; Fibrosis of extraocular muscles, congenital, 3A, MIM# 600638","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:59:42.479661+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6063","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB3 were set to ","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:59:16.139930+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6062","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:58:58.385981+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6061","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20829227, 25059107, 33318778, 20074521; Phenotypes: Cortical dysplasia, complex, with other brain malformations 1, MIM# 614039, Fibrosis of extraocular muscles, congenital, 3A, MIM# 600638; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:54:52.880778+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6061","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB2B as ready","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:54:52.871541+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6061","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2b has been classified as Green List (High Evidence).","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:54:44.546088+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6061","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB2B were changed from  to Cortical dysplasia, complex, with other brain malformations 7, MIM# 610031","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:54:26.646786+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6060","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB2B were set to ","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:54:05.297176+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6059","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:53:45.353240+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6058","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB2B: Rating: GREEN; Mode of pathogenicity: None; Publications: 19465910, 22333901, 26732629, 33082561; Phenotypes: Cortical dysplasia, complex, with other brain malformations 7, MIM# 610031; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:52:08.027868+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6058","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB as ready","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:52:08.019480+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6058","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb has been classified as Green List (High Evidence).","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:51:59.850904+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6058","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB were changed from  to Cortical dysplasia, complex, with other brain malformations 6, MIM# 615771","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:51:40.573632+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6057","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB were set to ","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:51:22.643001+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6056","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:51:04.321381+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6055","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB: Rating: GREEN; Mode of pathogenicity: None; Publications: 23246003, 32085672; Phenotypes: Cortical dysplasia, complex, with other brain malformations 6, MIM# 615771; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T21:10:49.667826+11:00","panel_name":"Tubulinopathies","panel_id":21,"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":"2021-01-16T21:10:34.882678+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBG1 as ready","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:10:34.874917+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubg1 has been classified as Green List (High Evidence).","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:10:31.989639+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBG1 were changed from  to Cortical dysplasia, complex, with other brain malformations 4, MIM# 615412","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:10:09.560039+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBG1 were set to ","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:09:38.576016+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:09:08.743514+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 31086189; Phenotypes: Cortical dysplasia, complex, with other brain malformations 4, MIM# 615412; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBG1","entity_type":"gene"},{"created":"2021-01-16T21:07:49.779085+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB3 as ready","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:07:49.771601+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb3 has been classified as Green List (High Evidence).","entity_name":"TUBB3","entity_type":"gene"}]}