{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1866","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1864","results":[{"created":"2020-04-12T21:49:19.941506+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2198","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBCD as ready","entity_name":"TBCD","entity_type":"gene"},{"created":"2020-04-12T21:49:19.932657+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2198","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbcd has been classified as Green List (High Evidence).","entity_name":"TBCD","entity_type":"gene"},{"created":"2020-04-12T21:49:09.748184+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2198","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBCD were changed from  to Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum, MIM#617193","entity_name":"TBCD","entity_type":"gene"},{"created":"2020-04-12T21:48:55.735044+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2197","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBCD were set to ","entity_name":"TBCD","entity_type":"gene"},{"created":"2020-04-12T21:48:23.513552+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2196","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBCD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBCD","entity_type":"gene"},{"created":"2020-04-12T21:47:31.790314+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2195","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMTC2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TMTC2","entity_type":"gene"},{"created":"2020-04-12T21:46:35.056683+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2194","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TMTC2 as Amber List (moderate evidence)","entity_name":"TMTC2","entity_type":"gene"},{"created":"2020-04-12T21:46:35.043332+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2194","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmtc2 has been classified as Amber List (Moderate Evidence).","entity_name":"TMTC2","entity_type":"gene"},{"created":"2020-04-12T21:45:39.869200+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UMOD as ready","entity_name":"UMOD","entity_type":"gene"},{"created":"2020-04-12T21:45:39.859272+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","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":"2020-04-12T21:45:25.129957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOR1AIP1 as ready","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2020-04-12T21:45:25.116401+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1aip1 has been classified as Green List (High Evidence).","entity_name":"TOR1AIP1","entity_type":"gene"},{"created":"2020-04-12T21:44:33.321172+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UPK3A as ready","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:44:33.307930+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: upk3a has been classified as Red List (Low Evidence).","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:44:32.422993+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2193","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UMOD were changed from  to Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886; Hyperuricemic nephropathy, familial juvenile 1 162000; Medullary cystic kidney disease 2 603860","entity_name":"UMOD","entity_type":"gene"},{"created":"2020-04-12T21:44:06.543286+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2192","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UMOD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886, Hyperuricemic nephropathy, familial juvenile 1 162000, Medullary cystic kidney disease 2 603860; Mode of inheritance: None","entity_name":"UMOD","entity_type":"gene"},{"created":"2020-04-12T21:42:30.916844+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2192","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UPK3A were changed from  to CAKUT","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:42:08.618846+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2191","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UPK3A were set to ","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:41:37.808089+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2190","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UPK3A as Red List (low evidence)","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:41:37.799624+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: upk3a has been classified as Red List (Low Evidence).","entity_name":"UPK3A","entity_type":"gene"},{"created":"2020-04-12T21:40:50.188361+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2189","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VARS as ready","entity_name":"VARS","entity_type":"gene"},{"created":"2020-04-12T21:40:50.175396+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2189","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vars has been classified as Green List (High Evidence).","entity_name":"VARS","entity_type":"gene"},{"created":"2020-04-12T21:40:41.478090+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VARS were changed from  to Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy; OMIM #617802","entity_name":"VARS","entity_type":"gene"},{"created":"2020-04-12T21:39:54.935286+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2188","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNT10A as ready","entity_name":"WNT10A","entity_type":"gene"},{"created":"2020-04-12T21:39:54.926004+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2188","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt10a has been classified as Green List (High Evidence).","entity_name":"WNT10A","entity_type":"gene"},{"created":"2020-04-12T21:39:50.333019+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF592 as ready","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:39:50.319065+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf592 has been classified as Red List (Low Evidence).","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:39:44.100098+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2188","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT10A were changed from  to Odontoonychodermal dysplasia; Schopf-Schulz-Passarge syndrome; Tooth agenesis, selective, 4","entity_name":"WNT10A","entity_type":"gene"},{"created":"2020-04-12T21:39:27.212100+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2187","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT10A were set to ","entity_name":"WNT10A","entity_type":"gene"},{"created":"2020-04-12T21:39:11.274722+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2186","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNT10A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WNT10A","entity_type":"gene"},{"created":"2020-04-12T21:38:16.825415+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF592 were changed from  to SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:37:52.914209+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF592 were set to ","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:37:27.778006+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF592 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:36:52.285712+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF592 as Red List (low evidence)","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:36:52.272502+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf592 has been classified as Red List (Low Evidence).","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:36:19.625498+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2185","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF592 as ready","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:36:19.616906+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2185","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf592 has been classified as Red List (Low Evidence).","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:36:11.485452+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF592: Rating: RED; Mode of pathogenicity: None; Publications: 20531441, 26123727; Phenotypes: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:35:42.649730+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2185","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF592 were changed from  to SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:34:42.877957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2184","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF592 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:33:51.940629+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2183","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF592 were set to ","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:33:37.776973+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2182","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF592 as Red List (low evidence)","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:33:37.763650+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2182","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf592 has been classified as Red List (Low Evidence).","entity_name":"ZNF592","entity_type":"gene"},{"created":"2020-04-12T21:32:29.657813+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLIC5 as ready","entity_name":"CLIC5","entity_type":"gene"},{"created":"2020-04-12T21:32:29.644683+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clic5 has been classified as Amber List (Moderate Evidence).","entity_name":"CLIC5","entity_type":"gene"},{"created":"2020-04-12T21:31:40.302415+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNB2 as ready","entity_name":"GNB2","entity_type":"gene"},{"created":"2020-04-12T21:31:40.293123+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnb2 has been classified as Amber List (Moderate Evidence).","entity_name":"GNB2","entity_type":"gene"},{"created":"2020-04-12T21:30:58.302396+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR96 as ready","entity_name":"MIR96","entity_type":"gene"},{"created":"2020-04-12T21:30:58.289099+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir96 has been classified as Amber List (Moderate Evidence).","entity_name":"MIR96","entity_type":"gene"},{"created":"2020-04-12T21:30:28.835126+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYL1 as ready","entity_name":"MYL1","entity_type":"gene"},{"created":"2020-04-12T21:30:28.826553+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYL1","entity_type":"gene"},{"created":"2020-04-12T21:29:19.145159+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: APOL1 as ready","entity_name":"APOL1","entity_type":"gene"},{"created":"2020-04-12T21:29:19.131974+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: apol1 has been classified as Red List (Low Evidence).","entity_name":"APOL1","entity_type":"gene"},{"created":"2020-04-12T21:28:41.015872+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARHGEF6 as ready","entity_name":"ARHGEF6","entity_type":"gene"},{"created":"2020-04-12T21:28:41.007402+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arhgef6 has been classified as Red List (Low Evidence).","entity_name":"ARHGEF6","entity_type":"gene"},{"created":"2020-04-12T21:27:55.564104+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP85L as ready","entity_name":"CEP85L","entity_type":"gene"},{"created":"2020-04-12T21:27:55.550891+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep85l has been classified as Green List (High Evidence).","entity_name":"CEP85L","entity_type":"gene"},{"created":"2020-04-12T21:27:46.374899+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP85L as Green List (high evidence)","entity_name":"CEP85L","entity_type":"gene"},{"created":"2020-04-12T21:27:46.365836+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep85l has been classified as Green List (High Evidence).","entity_name":"CEP85L","entity_type":"gene"},{"created":"2020-04-12T21:26:27.601001+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIEF2 as ready","entity_name":"MIEF2","entity_type":"gene"},{"created":"2020-04-12T21:26:27.587819+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mief2 has been classified as Red List (Low Evidence).","entity_name":"MIEF2","entity_type":"gene"},{"created":"2020-04-12T21:25:48.534344+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLE2 as ready","entity_name":"POLE2","entity_type":"gene"},{"created":"2020-04-12T21:25:48.525617+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pole2 has been classified as Red List (Low Evidence).","entity_name":"POLE2","entity_type":"gene"},{"created":"2020-04-12T21:25:19.581205+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTCD1 as ready","entity_name":"PTCD1","entity_type":"gene"},{"created":"2020-04-12T21:25:19.567575+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ptcd1 has been classified as Red List (Low Evidence).","entity_name":"PTCD1","entity_type":"gene"},{"created":"2020-04-12T21:24:39.473389+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TFAM as ready","entity_name":"TFAM","entity_type":"gene"},{"created":"2020-04-12T21:24:39.461917+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfam has been classified as Amber List (Moderate Evidence).","entity_name":"TFAM","entity_type":"gene"},{"created":"2020-04-12T21:24:30.451604+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TFAM as Amber List (moderate evidence)","entity_name":"TFAM","entity_type":"gene"},{"created":"2020-04-12T21:24:30.438782+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfam has been classified as Amber List (Moderate Evidence).","entity_name":"TFAM","entity_type":"gene"},{"created":"2020-04-12T21:22:38.680842+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2179","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NME3 as ready","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T21:22:38.671531+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nme3 has been classified as Red List (Low Evidence).","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T21:22:27.943706+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2179","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NME3 was added\ngene: NME3 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: NME3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NME3 were set to 30587587\nPhenotypes for gene: NME3 were set to Hypotonia; Neurodegeneration; Abnormal mitochondrial dynamics\nReview for gene: NME3 was set to RED\nAdded comment: Single individual reported. NME3 is a mitochondrial outer-membrane protein capable of interacting with MFN1/2, and its depletion causes dysfunction in mitochondrial dynamics \nSources: Expert list","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T21:20:48.440100+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.348","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NME3 as ready","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T21:20:48.431029+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.348","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nme3 has been classified as Red List (Low Evidence).","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T18:31:15.548457+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.348","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NME3 was added\ngene: NME3 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: NME3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NME3 were set to 30587587\nPhenotypes for gene: NME3 were set to Hypotonia; Neurodegeneration; Abnormal mitochondrial dynamics\nReview for gene: NME3 was set to RED\nAdded comment: Single individual reported. NME3 is a mitochondrial outer-membrane protein capable of interacting with MFN1/2, and its depletion causes dysfunction in mitochondrial dynamics. \nSources: Expert list","entity_name":"NME3","entity_type":"gene"},{"created":"2020-04-12T18:22:11.135948+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2178","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRPS28 as ready","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:22:11.122799+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2178","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps28 has been classified as Red List (Low Evidence).","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:21:57.674974+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2178","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MRPS28 was added\ngene: MRPS28 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MRPS28 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS28 were set to 30566640\nPhenotypes for gene: MRPS28 were set to Intrauterine growth retardation; developmental delay; dysmorphism\nReview for gene: MRPS28 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:20:22.917608+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRPS28 as ready","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:20:22.904332+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps28 has been classified as Red List (Low Evidence).","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:20:13.814639+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MRPS28 was added\ngene: MRPS28 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: MRPS28 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS28 were set to 30566640\nPhenotypes for gene: MRPS28 were set to Intrauterine growth retardation; developmental delay; dysmorphism\nReview for gene: MRPS28 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"MRPS28","entity_type":"gene"},{"created":"2020-04-12T18:17:15.012306+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2177","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRPS25 as ready","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:17:14.996221+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2177","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps25 has been classified as Red List (Low Evidence).","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:17:05.497475+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2177","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MRPS25 was added\ngene: MRPS25 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MRPS25 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS25 were set to 31039582\nPhenotypes for gene: MRPS25 were set to Dyskinetic cerebral palsy; Mitochondrial myopathy; Partial agenesis of the corpus callosum\nReview for gene: MRPS25 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:15:34.327173+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.346","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRPS25 as ready","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:15:34.314390+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.346","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps25 has been classified as Red List (Low Evidence).","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:15:26.892004+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.346","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MRPS25 was added\ngene: MRPS25 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: MRPS25 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS25 were set to 31039582\nPhenotypes for gene: MRPS25 were set to Dyskinetic cerebral palsy; Mitochondrial myopathy; Partial agenesis of the corpus callosum\nReview for gene: MRPS25 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list","entity_name":"MRPS25","entity_type":"gene"},{"created":"2020-04-12T18:12:09.823358+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2176","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MRPS23 were changed from Hepatic disease; Combined respiratory chain complex deficiencies to Hepatic disease; Combined respiratory chain complex deficienciesHepatic disease; Combined respiratory chain complex deficiencies; Cardiomyopathy; Tubulopathy; Lactic acidosis; Structural brain abnormalities","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:11:49.060993+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2175","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MRPS23 were set to 26741492","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:11:21.062911+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2174","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MRPS23 as Green List (high evidence)","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:11:21.049881+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2174","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps23 has been classified as Green List (High Evidence).","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:11:00.551586+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2173","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:10:52.822127+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2173","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MRPS23: Added comment: Four families reported.; Changed rating: GREEN; Changed publications: 26741492, 17873122, 25663021, 28752220; Changed phenotypes: Hepatic disease, Combined respiratory chain complex deficiencies, Cardiomyopathy, Tubulopathy, Lactic acidosis, Structural brain abnormalities","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:09:54.863181+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.345","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MRPS23 were changed from Hepatic disease; Combined respiratory chain complex deficiencies to Hepatic disease; Combined respiratory chain complex deficiencies; Cardiomyopathy; Tubulopathy; Lactic acidosis; Structural brain abnormalities","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:09:02.989477+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MRPS23 were set to 26741492","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:08:30.196675+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MRPS23 as Green List (high evidence)","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:08:30.188055+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps23 has been classified as Green List (High Evidence).","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:07:50.949729+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MRPS23: Changed rating: GREEN","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:07:43.256384+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single family reported.; to: Four families reported.","entity_name":"MRPS23","entity_type":"gene"},{"created":"2020-04-12T18:07:32.976850+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MRPS23: Changed publications: 26741492, 17873122, 25663021, 28752220; Changed phenotypes: Hepatic disease, Combined respiratory chain complex deficiencies, Cardiomyopathy, Tubulopathy, Lactic acidosis, Structural brain abnormalities","entity_name":"MRPS23","entity_type":"gene"}]}