{"count":220864,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1961","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1959","results":[{"created":"2020-01-26T18:10:16.183885+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.536","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF142 as ready","entity_name":"ZNF142","entity_type":"gene"},{"created":"2020-01-26T18:10:16.176032+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.536","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf142 has been classified as Green List (High Evidence).","entity_name":"ZNF142","entity_type":"gene"},{"created":"2020-01-26T18:10:11.032721+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.536","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM#604317","entity_name":"WDR62","entity_type":"gene"},{"created":"2020-01-26T18:09:25.069721+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.535","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF142 as Green List (high evidence)","entity_name":"ZNF142","entity_type":"gene"},{"created":"2020-01-26T18:09:25.056373+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.535","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf142 has been classified as Green List (High Evidence).","entity_name":"ZNF142","entity_type":"gene"},{"created":"2020-01-26T18:08:52.292307+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.534","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2020-01-26T18:08:19.774163+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.534","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZNF142 was added\ngene: ZNF142 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: ZNF142 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZNF142 were set to 31036918\nPhenotypes for gene: ZNF142 were set to Neurodevelopmental disorder with impaired speech and hyperkinetic movements, MIM#618425\nReview for gene: ZNF142 was set to GREEN\ngene: ZNF142 was marked as current diagnostic\nAdded comment: Seven individuals from four unrelated families; 5/7 had seizures. \nSources: Expert list","entity_name":"ZNF142","entity_type":"gene"},{"created":"2020-01-26T18:06:43.030214+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.533","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2020-01-26T18:05:00.761792+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.532","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZDHHC9 as ready","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2020-01-26T18:05:00.754090+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.532","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zdhhc9 has been classified as Green List (High Evidence).","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2020-01-26T18:04:51.312270+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.532","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZDHHC9 as Green List (high evidence)","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2020-01-26T18:04:51.305631+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.532","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zdhhc9 has been classified as Green List (High Evidence).","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2020-01-26T18:03:35.202386+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.531","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZDHHC9 was added\ngene: ZDHHC9 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: ZDHHC9 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: ZDHHC9 were set to 26000327\nPhenotypes for gene: ZDHHC9 were set to Mental retardation, X-linked syndromic, Raymond type, MIM#300799\nReview for gene: ZDHHC9 was set to GREEN\ngene: ZDHHC9 was marked as current diagnostic\nAdded comment: A third of reported individuals have had seizures. \nSources: Expert list","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2020-01-26T18:01:33.070525+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR45B as ready","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T18:01:33.055469+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr45b has been classified as Green List (High Evidence).","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T18:00:06.044649+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 21834044, 20890278, 20729831; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM#604317; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2020-01-26T17:59:31.512261+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR45B were changed from  to Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures, MIM# 617977","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T17:55:06.948370+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.529","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR45B were set to ","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T17:54:21.705875+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.528","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR45B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T17:53:35.499432+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR45B: Rating: GREEN; Mode of pathogenicity: None; Publications: 21937992, 28503735, 27431290; Phenotypes: Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures, MIM# 617977; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR45B","entity_type":"gene"},{"created":"2020-01-26T17:47:11.166606+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1687","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WARS2 as Green List (high evidence)","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:47:11.159604+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1687","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wars2 has been classified as Green List (High Evidence).","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:45:56.352603+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1686","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WARS2 was added\ngene: WARS2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: WARS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WARS2 were set to 29783990; 28236339; 29120065; 28650581; 28905505\nPhenotypes for gene: WARS2 were set to Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, MIM#617710\nReview for gene: WARS2 was set to GREEN\ngene: WARS2 was marked as current diagnostic\nAdded comment: 7 unrelated families reported. \nSources: Expert list","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:45:13.056077+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WARS2 as ready","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:45:13.048188+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wars2 has been classified as Green List (High Evidence).","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:44:38.088162+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WARS2 as Green List (high evidence)","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:44:38.081291+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wars2 has been classified as Green List (High Evidence).","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:43:33.957074+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.526","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WARS2 was added\ngene: WARS2 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: WARS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WARS2 were set to 29783990; 28236339; 29120065; 28650581; 28905505\nPhenotypes for gene: WARS2 were set to Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, MIM#617710\nReview for gene: WARS2 was set to GREEN\ngene: WARS2 was marked as current diagnostic\nAdded comment: 7 unrelated families reported, most affected individuals had seizures as part of this mitochondrial disorder. \nSources: Expert list","entity_name":"WARS2","entity_type":"gene"},{"created":"2020-01-26T17:39:48.559538+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1685","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS11 as ready","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:39:48.552869+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1685","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps11 has been classified as Green List (High Evidence).","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:39:36.086028+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1685","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VPS11 as Green List (high evidence)","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:39:36.078522+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1685","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps11 has been classified as Green List (High Evidence).","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:38:39.966758+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1684","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS11 was added\ngene: VPS11 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: VPS11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS11 were set to 27120463; 26307567; 27473128\nPhenotypes for gene: VPS11 were set to Leukodystrophy, hypomyelinating, 12, MIM#616683\nReview for gene: VPS11 was set to GREEN\nAdded comment: ID, (variable) acquired microcephaly with hypomyelination; seizures in several reported individuals. 13 individuals from 7 Ashkenazi Jewish families, homozygous for a founder mutation (NM_021729.5:c.2536T>G or p.Cys846Gly); a different variant (p.Leu387_Gly395del) reported in a consanguineous family. \nSources: Expert list","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:37:57.613516+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.525","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS11 as ready","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:37:57.605751+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.525","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps11 has been classified as Green List (High Evidence).","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:37:10.046606+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.525","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VPS11 as Green List (high evidence)","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:37:10.034020+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.525","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps11 has been classified as Green List (High Evidence).","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:35:55.992822+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.524","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS11 was added\ngene: VPS11 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: VPS11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS11 were set to 27120463; 26307567; 27473128\nPhenotypes for gene: VPS11 were set to Leukodystrophy, hypomyelinating, 12, MIM#616683\nReview for gene: VPS11 was set to GREEN\ngene: VPS11 was marked as current diagnostic\nAdded comment: ID, (variable) acquired microcephaly with hypomyelination; seizures in several reported individuals.\r\n\r\n13 individuals from 7 Ashkenazi Jewish families, homozygous for a founder mutation (NM_021729.5:c.2536T>G or p.Cys846Gly); a different variant (p.Leu387_Gly395del) reported in a consanguineous family. \nSources: Expert list","entity_name":"VPS11","entity_type":"gene"},{"created":"2020-01-26T17:35:31.679060+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.523","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VLDLR as ready","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:35:30.879050+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.523","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vldlr has been classified as Amber List (Moderate Evidence).","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:31:51.106092+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.523","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VLDLR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:30:26.840018+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.522","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VLDLR were changed from  to Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, MIM#224050","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:29:56.243612+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.522","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VLDLR were set to ","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:28:43.180268+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VLDLR as Amber List (moderate evidence)","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:28:43.172048+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vldlr has been classified as Amber List (Moderate Evidence).","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:28:01.896600+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VLDLR: Rating: AMBER; Mode of pathogenicity: None; Publications: 16174313, 18326629; Phenotypes: Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, MIM#224050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VLDLR","entity_type":"gene"},{"created":"2020-01-26T17:25:37.469221+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAMP2 as ready","entity_name":"VAMP2","entity_type":"gene"},{"created":"2020-01-26T17:25:37.461908+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vamp2 has been classified as Green List (High Evidence).","entity_name":"VAMP2","entity_type":"gene"},{"created":"2020-01-26T17:24:43.136446+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VAMP2 as Green List (high evidence)","entity_name":"VAMP2","entity_type":"gene"},{"created":"2020-01-26T17:24:43.128423+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vamp2 has been classified as Green List (High Evidence).","entity_name":"VAMP2","entity_type":"gene"},{"created":"2020-01-26T17:23:47.212196+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.519","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VAMP2 was added\ngene: VAMP2 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: VAMP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: VAMP2 were set to 30929742\nPhenotypes for gene: VAMP2 were set to Cortical visual impairment; Seizures; Stereotypic behaviour; Generalized hypotonia; Intellectual disability\nReview for gene: VAMP2 was set to GREEN\ngene: VAMP2 was marked as current diagnostic\nAdded comment: Five unrelated individuals reported, three had seizures as part of the phenotype of this neurodevelopmental condition. \nSources: Expert list","entity_name":"VAMP2","entity_type":"gene"},{"created":"2020-01-26T16:22:10.442246+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB2A as ready","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2020-01-26T16:22:10.434911+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2a has been classified as Green List (High Evidence).","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2020-01-26T16:22:00.595535+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TUBB2A as Green List (high evidence)","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2020-01-26T16:22:00.588365+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2a has been classified as Green List (High Evidence).","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2020-01-26T16:21:01.532310+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.517","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB2A was added\ngene: TUBB2A was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: TUBB2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TUBB2A were set to 24702957; 25326637\nPhenotypes for gene: TUBB2A were set to Cortical dysplasia, complex, with other brain malformations 5, MIM#615763\nReview for gene: TUBB2A was set to GREEN\ngene: TUBB2A was marked as current diagnostic\nAdded comment: Seizures are part of the phenotype of the tubulinopathies. \nSources: Expert list","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2020-01-26T15:19:08.062868+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.516","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBA8 as ready","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:19:08.053985+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.516","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tuba8 has been classified as Green List (High Evidence).","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:19:00.124718+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.516","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBA8 were changed from Cortical dysplasia, complex, with other brain malformations 8, MIM#613180 to Cortical dysplasia, complex, with other brain malformations 8, MIM#613180","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:18:25.210625+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.515","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBA8 were changed from  to Cortical dysplasia, complex, with other brain malformations 8, MIM#613180","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:17:51.796241+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.514","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBA8 were set to ","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:17:11.909635+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.513","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:16:30.950763+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBA8: Rating: GREEN; Mode of pathogenicity: None; Publications: 31481326, 19896110; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM#613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TUBA8","entity_type":"gene"},{"created":"2020-01-26T15:14:22.358853+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSFM as ready","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-26T15:14:22.351514+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsfm has been classified as Green List (High Evidence).","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-26T15:14:12.961096+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSFM were changed from  to Combined oxidative phosphorylation deficiency 3, MIM#610505","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-26T15:13:38.112593+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.511","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSFM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-26T15:12:54.672681+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSFM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Combined oxidative phosphorylation deficiency 3, MIM#610505; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-26T15:08:04.133880+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSEN2 as ready","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:08:04.123999+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsen2 has been classified as Green List (High Evidence).","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:07:52.598143+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSEN2 were changed from  to Pontocerebellar hypoplasia, type 2F, MIM#617026","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:07:18.772224+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.509","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSEN2 were set to ","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:06:41.017068+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSEN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:05:58.815689+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSEN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23562994, 18711368, 20952379; Phenotypes: Pontocerebellar hypoplasia, type 2F, MIM#617026; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSEN2","entity_type":"gene"},{"created":"2020-01-26T15:02:23.482408+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRRAP as ready","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T15:02:23.475809+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trrap has been classified as Green List (High Evidence).","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T15:02:10.806137+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRRAP were changed from  to Developmental delay with or without dysmorphic facies and autism, MIM#618454","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T15:01:35.000759+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRRAP were set to ","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T15:00:58.888125+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.505","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRRAP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T15:00:17.164304+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRRAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 30827496, 28628100; Phenotypes: Developmental delay with or without dysmorphic facies and autism, MIM#618454; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRRAP","entity_type":"gene"},{"created":"2020-01-26T14:47:05.932219+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRPM6 as ready","entity_name":"TRPM6","entity_type":"gene"},{"created":"2020-01-26T14:47:05.925224+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trpm6 has been classified as Green List (High Evidence).","entity_name":"TRPM6","entity_type":"gene"},{"created":"2020-01-26T14:46:57.235361+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRPM6 as Green List (high evidence)","entity_name":"TRPM6","entity_type":"gene"},{"created":"2020-01-26T14:46:57.228355+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trpm6 has been classified as Green List (High Evidence).","entity_name":"TRPM6","entity_type":"gene"},{"created":"2020-01-26T14:45:58.941458+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPM6 was added\ngene: TRPM6 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: TRPM6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRPM6 were set to Hypomagnesemia 1, intestinal, MIM#602014\nReview for gene: TRPM6 was set to GREEN\ngene: TRPM6 was marked as current diagnostic\nAdded comment: Can present with seizures. \nSources: Expert list","entity_name":"TRPM6","entity_type":"gene"},{"created":"2020-01-25T20:41:13.000482+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC12 as ready","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:41:12.993298+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Amber List (Moderate Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:40:25.064210+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1683","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAPPC12 as Green List (high evidence)","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:40:25.056381+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1683","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:54.234579+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Additional unpublished case reported by GEL.","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:54.204635+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC12 were set to 28777934","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:32.300840+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAPPC12 as ready","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:31.935499+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Additional unpublished case reported by GEL PanelApp.","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:30.629237+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:23.391684+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAPPC12 as Green List (high evidence)","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:39:23.360542+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:38:52.678529+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Additional unpublished case reported by GEL.","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:38:52.663510+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC12 were set to 28777934","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:38:21.115646+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAPPC12 as Green List (high evidence)","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2020-01-25T20:38:21.083649+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1682","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"}]}