{"count":220377,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=943","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=941","results":[{"created":"2022-03-09T19:42:12.878789+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11246","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT18 as ready","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:42:12.867134+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11246","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt18 has been classified as Red List (Low Evidence).","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:42:04.846612+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11246","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT18 were changed from  to Cirrhosis, cryptogenic , MIM#215600","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:41:21.000243+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11245","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT18 were set to ","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:38:02.732094+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11244","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT18 as Red List (low evidence)","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:38:02.716620+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11244","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt18 has been classified as Red List (Low Evidence).","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:37:28.856765+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11243","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT18: Rating: RED; Mode of pathogenicity: None; Publications: 9011570, 27689336, 20538000; Phenotypes: Cirrhosis, cryptogenic , MIM#215600; Mode of inheritance: None","entity_name":"KRT18","entity_type":"gene"},{"created":"2022-03-09T19:33:22.144459+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11243","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT25 as ready","entity_name":"KRT25","entity_type":"gene"},{"created":"2022-03-09T19:33:22.134575+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11243","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt25 has been classified as Green List (High Evidence).","entity_name":"KRT25","entity_type":"gene"},{"created":"2022-03-09T19:33:14.242104+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11243","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT25 were changed from  to Woolly hair, autosomal recessive 3 MIM#616760","entity_name":"KRT25","entity_type":"gene"},{"created":"2022-03-09T19:32:56.793985+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11242","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT25 were set to ","entity_name":"KRT25","entity_type":"gene"},{"created":"2022-03-09T19:32:36.307892+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11241","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT25 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"KRT25","entity_type":"gene"},{"created":"2022-03-09T19:31:43.790382+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11240","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT4 as ready","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:31:43.778812+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11240","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt4 has been classified as Green List (High Evidence).","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:31:35.520242+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11240","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT4 were changed from  to White sponge naevus 1, MIM# 193900","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:28:35.705802+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11239","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT4 were set to ","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:28:13.711447+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11238","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:27:55.101355+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11237","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT4: Rating: GREEN; Mode of pathogenicity: None; Publications: 7493030, 10652003, 12828738; Phenotypes: White sponge naevus 1, MIM# 193900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT4","entity_type":"gene"},{"created":"2022-03-09T19:23:52.808243+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11237","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT74 as ready","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:23:52.798271+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11237","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Amber List (Moderate Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:15:15.119399+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11237","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT74 were changed from  to Ectodermal dysplasia 7, hair/nail type MIM#614929; Hypotrichosis 3 , MIM# 613981; Woolly hair, autosomal dominant, MIM# 194300","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:59.095692+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11236","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT74 were set to ","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:45.819721+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11235","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT74 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:26.947973+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11234","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT74 as Amber List (moderate evidence)","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:26.931911+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11234","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Amber List (Moderate Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:11.124508+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT74 as ready","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:11.113072+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Amber List (Moderate Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:09.294125+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT74 were changed from Hypotrichosis 3, 613981 to Hypotrichosis 3 , MIM# 613981; Woolly hair, autosomal dominant, MIM# 194300","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:14:02.533209+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT74 were set to ","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:13:53.509287+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT74 as Amber List (moderate evidence)","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:13:53.497992+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Amber List (Moderate Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:13:45.820177+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT74: Rating: AMBER; Mode of pathogenicity: None; Publications: 21188418, 20346438, 21188418; Phenotypes: Hypotrichosis 3 , MIM# 613981, Woolly hair, autosomal dominant, MIM# 194300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:13:02.680964+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT74 as ready","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:13:02.657440+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Red List (Low Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:12:56.366783+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT74 as Red List (low evidence)","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:12:56.354073+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt74 has been classified as Red List (Low Evidence).","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:12:44.094449+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT74: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ectodermal dysplasia 7, hair/nail type MIM#614929; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:12:19.124981+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11233","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT74: Rating: AMBER; Mode of pathogenicity: None; Publications: 24714551, 21188418, 20346438, 21188418; Phenotypes: Ectodermal dysplasia 7, hair/nail type MIM#614929, Hypotrichosis 3 , MIM# 613981, Woolly hair, autosomal dominant, MIM# 194300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"KRT74","entity_type":"gene"},{"created":"2022-03-09T19:04:49.083661+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11233","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT75 as ready","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:04:49.069086+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11233","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt75 has been classified as Red List (Low Evidence).","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:04:41.819466+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11233","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT75 were changed from  to {Pseudofolliculitis barbae, susceptibility to} 612318","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:04:18.432265+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11232","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT75 as Red List (low evidence)","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:04:18.419995+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11232","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt75 has been classified as Red List (Low Evidence).","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:04:00.951144+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11231","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT75: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Pseudofolliculitis barbae, susceptibility to} 612318; Mode of inheritance: None","entity_name":"KRT75","entity_type":"gene"},{"created":"2022-03-09T19:03:08.482982+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11231","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT81 as ready","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:03:08.468770+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11231","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt81 has been classified as Green List (High Evidence).","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:53.964631+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT81 as ready","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:53.948858+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt81 has been classified as Green List (High Evidence).","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:50.947760+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT81 were changed from Monilethrix, 158000 to Monilethrix, MIM# 158000","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:41.755048+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT81 were set to 31332722","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:22.871540+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT81: Rating: GREEN; Mode of pathogenicity: None; Publications: 9402962, 22628999; Phenotypes: Monilethrix, MIM# 158000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:02:17.317193+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11231","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT81 were changed from  to Monilethrix, MIM# 158000","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:01:59.196570+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11230","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT81 were set to ","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:01:40.969325+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11229","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT81 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T19:01:22.611130+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11228","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT81: Rating: GREEN; Mode of pathogenicity: None; Publications: 9402962, 22628999; Phenotypes: Monilethrix, MIM# 158000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT81","entity_type":"gene"},{"created":"2022-03-09T18:02:22.167493+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC80 were changed from Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability to Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, MIM# 616801; MONDO:0014777","entity_name":"UNC80","entity_type":"gene"},{"created":"2022-03-09T18:01:56.661635+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.8","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UNC80 as Amber List (moderate evidence)","entity_name":"UNC80","entity_type":"gene"},{"created":"2022-03-09T18:01:56.650295+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc80 has been classified as Amber List (Moderate Evidence).","entity_name":"UNC80","entity_type":"gene"},{"created":"2022-03-09T18:01:02.423515+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NARS2 as ready","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T18:01:02.408914+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars2 has been classified as Green List (High Evidence).","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T18:00:56.465848+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NARS2 were changed from  to Combined oxidative phosphorylation deficiency 24 - MIM#616239; Deafness, autosomal recessive 94 - MIM#618434","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T18:00:13.970608+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NARS2 were set to ","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:59:30.848962+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:58:41.025368+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11228","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NARS2 as ready","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:58:41.013945+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11228","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars2 has been classified as Green List (High Evidence).","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:58:32.946498+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11228","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NARS2 were changed from  to Combined oxidative phosphorylation deficiency 24 - MIM#616239; Deafness, autosomal recessive 94 - MIM#618434","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:58:05.071436+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11227","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NARS2 were set to ","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:57:43.521384+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11226","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:56:58.732914+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1469","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NARS2 as ready","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:56:58.727776+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1469","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Refractory seizures are part of the phenotype.","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:56:58.687564+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1469","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars2 has been classified as Green List (High Evidence).","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:56:55.576296+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NARS2 were changed from  to Combined oxidative phosphorylation deficiency 24 - MIM#616239","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:56:22.769863+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NARS2 were set to ","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:55:45.887788+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NARS2","entity_type":"gene"},{"created":"2022-03-09T17:54:56.986167+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11225","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNPLA3 as ready","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:54:56.972953+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11225","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnpla3 has been classified as Red List (Low Evidence).","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:54:48.025239+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11225","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PNPLA3 were changed from  to Susceptibility to nonalcoholic fatty liver disease","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:54:26.501929+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11224","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PNPLA3 were set to ","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:54:05.296997+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11223","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PNPLA3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:53:47.060396+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11222","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PNPLA3 as Red List (low evidence)","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:53:47.046520+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnpla3 has been classified as Red List (Low Evidence).","entity_name":"PNPLA3","entity_type":"gene"},{"created":"2022-03-09T17:52:32.725599+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NARS as ready","entity_name":"NARS","entity_type":"gene"},{"created":"2022-03-09T17:52:32.714271+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars has been classified as Green List (High Evidence).","entity_name":"NARS","entity_type":"gene"},{"created":"2022-03-09T17:52:27.309862+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NARS as Green List (high evidence)","entity_name":"NARS","entity_type":"gene"},{"created":"2022-03-09T17:52:27.298777+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars has been classified as Green List (High Evidence).","entity_name":"NARS","entity_type":"gene"},{"created":"2022-03-09T17:51:54.968107+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.112","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: NARS.","entity_name":"NARS","entity_type":"gene"},{"created":"2022-03-09T17:51:26.128009+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4546","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NANS as ready","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:51:26.116275+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4546","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nans has been classified as Green List (High Evidence).","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:50:52.857818+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4546","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NANS were changed from  to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type - MIM#610442","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:50:19.508449+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4545","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NANS were set to ","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:49:45.568115+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4544","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NANS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:48:32.824308+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11221","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NANS as ready","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:48:32.814805+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11221","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nans has been classified as Green List (High Evidence).","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:48:23.057038+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11221","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NANS were changed from  to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type - MIM#610442","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:48:02.914808+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11220","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NANS were set to ","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T17:47:41.877386+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11219","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NANS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NANS","entity_type":"gene"},{"created":"2022-03-09T16:44:37.096328+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.7","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: UNC80: Rating: AMBER; Mode of pathogenicity: None; Publications: 26545877; Phenotypes: Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, MIM# 616801, MONDO:0014777; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"UNC80","entity_type":"gene"},{"created":"2022-03-09T16:41:42.854382+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11218","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: S1PR2 as ready","entity_name":"S1PR2","entity_type":"gene"},{"created":"2022-03-09T16:41:42.844618+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11218","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: s1pr2 has been classified as Green List (High Evidence).","entity_name":"S1PR2","entity_type":"gene"},{"created":"2022-03-09T16:41:28.554770+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11218","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: S1PR2 were changed from  to Deafness, autosomal recessive 68, MIM# 610419","entity_name":"S1PR2","entity_type":"gene"}]}