{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1902","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1900","results":[{"created":"2020-03-18T12:30:32.565916+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDHB were changed from  to Complex II deficiency; mitochondrial leucoencephalopathy","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:30:05.037751+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SDHB were set to ","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:29:42.607325+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SDHB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:29:19.934779+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SDHB as Amber List (moderate evidence)","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:29:19.926391+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdhb has been classified as Amber List (Moderate Evidence).","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:28:48.971018+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SDHB: Rating: AMBER; Mode of pathogenicity: None; Publications: 22972948, 26925370; Phenotypes: Complex II deficiency, mitochondrial leucoencephalopathy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDHB","entity_type":"gene"},{"created":"2020-03-18T12:20:48.395288+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDHAF2 as ready","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:20:48.386665+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdhaf2 has been classified as Red List (Low Evidence).","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:20:42.789403+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDHAF2 were changed from  to Paragangliomas 2, MIM# 601650","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:20:20.480050+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SDHAF2 as Red List (low evidence)","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:20:20.466563+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdhaf2 has been classified as Red List (Low Evidence).","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:19:52.386187+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SDHAF2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 2, MIM# 601650; Mode of inheritance: None","entity_name":"SDHAF2","entity_type":"gene"},{"created":"2020-03-18T12:15:10.008883+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SACS as ready","entity_name":"SACS","entity_type":"gene"},{"created":"2020-03-18T12:15:09.998066+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sacs has been classified as Green List (High Evidence).","entity_name":"SACS","entity_type":"gene"},{"created":"2020-03-18T12:15:05.935621+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SACS as Green List (high evidence)","entity_name":"SACS","entity_type":"gene"},{"created":"2020-03-18T12:15:05.927476+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sacs has been classified as Green List (High Evidence).","entity_name":"SACS","entity_type":"gene"},{"created":"2020-03-18T12:14:37.582949+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SACS was added\ngene: SACS was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: SACS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SACS were set to 22307627; 20876471\nPhenotypes for gene: SACS were set to Spastic ataxia, Charlevoix-Saguenay type, MIM#\t270550\nReview for gene: SACS was set to GREEN\nAdded comment: Progressive neurological disorder, multiple families reported, mitochondrial dysfunction. \nSources: Expert list","entity_name":"SACS","entity_type":"gene"},{"created":"2020-03-18T12:06:00.355167+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDK3 as ready","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T12:06:00.346012+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdk3 has been classified as Green List (High Evidence).","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T12:05:56.800946+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDK3 were changed from  to Charcot-Marie-Tooth disease, X-linked dominant, 6, MIM# 300905","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T12:05:33.929846+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDK3 were set to ","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T12:05:11.541931+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDK3 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T12:04:41.670231+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PDK3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23297365, 28902413, 26801680; Phenotypes: Charcot-Marie-Tooth disease, X-linked dominant, 6, MIM# 300905; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"PDK3","entity_type":"gene"},{"created":"2020-03-18T11:57:34.644340+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PC as ready","entity_name":"PC","entity_type":"gene"},{"created":"2020-03-18T11:57:34.634677+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pc has been classified as Green List (High Evidence).","entity_name":"PC","entity_type":"gene"},{"created":"2020-03-18T11:57:29.987201+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PC as Green List (high evidence)","entity_name":"PC","entity_type":"gene"},{"created":"2020-03-18T11:57:29.974600+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pc has been classified as Green List (High Evidence).","entity_name":"PC","entity_type":"gene"},{"created":"2020-03-18T11:57:00.828818+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PC was added\ngene: PC was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: PC was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PC were set to Pyruvate carboxylase deficiency, MIM#\t266150\nReview for gene: PC was set to GREEN\nAdded comment: Multiple families reported. Spectrum of severity ranging from death in infancy to a relatively benign condition. Correlates with variant impact with more severely affected individuals having at least one truncating variant. \nSources: Expert list","entity_name":"PC","entity_type":"gene"},{"created":"2020-03-18T11:35:32.595878+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1743","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFS1 as ready","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:35:32.587090+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1743","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfs1 has been classified as Red List (Low Evidence).","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:34:07.554516+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1743","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFS1 were changed from  to Complex II/III deficiency; multisystem organ failure","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:33:57.440635+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFS1 as ready","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:33:57.427700+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfs1 has been classified as Red List (Low Evidence).","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:33:53.811968+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFS1 were changed from  to Complex II/III deficiency; multisystem organ failure","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:33:22.789078+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1742","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NFS1 were set to ","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:59.327085+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1741","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:44.208614+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1740","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFS1 as Red List (low evidence)","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:44.194747+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1740","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfs1 has been classified as Red List (Low Evidence).","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:37.156691+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NFS1 were set to ","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:26.386625+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1739","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NFS1: Rating: RED; Mode of pathogenicity: None; Publications: 24498631; Phenotypes: Complex II/III deficiency, multisystem organ failure; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:32:09.095068+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:31:38.729118+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFS1 as Red List (low evidence)","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:31:38.720233+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfs1 has been classified as Red List (Low Evidence).","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:31:09.742616+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NFS1: Rating: RED; Mode of pathogenicity: None; Publications: 24498631; Phenotypes: Complex II/III deficiency, multisystem organ failure; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NFS1","entity_type":"gene"},{"created":"2020-03-18T11:23:34.966267+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA6 as ready","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:23:34.957469+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa6 has been classified as Green List (High Evidence).","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:23:19.390722+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA6 were changed from  to Mitochondrial complex I deficiency, nuclear type 33, MIM# 618253","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:22:57.566370+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1738","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA6 were set to ","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:22:38.072809+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1737","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:22:18.677505+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1736","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA6: Rating: GREEN; Mode of pathogenicity: None; Publications: 30245030; Phenotypes: Mitochondrial complex I deficiency, nuclear type 33, MIM# 618253; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:21:12.486552+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA6 as ready","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:21:12.473844+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa6 has been classified as Green List (High Evidence).","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:21:08.612877+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA6 as Green List (high evidence)","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:21:08.600201+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa6 has been classified as Green List (High Evidence).","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:20:41.080078+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NDUFA6 was added\ngene: NDUFA6 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: NDUFA6 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NDUFA6 were set to 30245030\nPhenotypes for gene: NDUFA6 were set to Mitochondrial complex I deficiency, nuclear type 33, MIM#\t618253\nReview for gene: NDUFA6 was set to GREEN\ngene: NDUFA6 was marked as current diagnostic\nAdded comment: Four unrelated children reported with bi-allelic variants in this gene and delayed development and/or neurologic deterioration in the first weeks or years of life. Two individuals died in infancy; the other 2 were unable to stand, walk, or speak, and had optic atrophy. \nSources: Expert list","entity_name":"NDUFA6","entity_type":"gene"},{"created":"2020-03-18T11:17:00.666676+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA4 as ready","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:17:00.646907+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:16:51.668573+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA4 as ready","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:16:51.653308+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Red List (Low Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:16:45.782143+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA4 were changed from  to Leigh syndrome; Complex IV deficiency","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:15:25.725575+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA4 were set to ","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:15:00.744232+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA4 as Red List (low evidence)","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:15:00.732367+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Red List (Low Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:14:40.977501+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA4 were changed from  to Leigh syndrome; Complex IV deficiency","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:14:30.372963+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA4: Rating: RED; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: None","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:12:41.002066+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA4 as ready","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:12:40.992927+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:11:35.244968+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1736","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA4 were changed from  to Leigh syndrome; Complex IV deficiency","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:11:21.795732+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1735","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA4 were set to ","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:11:05.827904+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1734","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:10:42.581232+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1733","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA4 as Amber List (moderate evidence)","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:10:42.568097+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1733","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:10:19.799306+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1732","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA4: Rating: AMBER; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:10:09.195409+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA4 were set to ","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:09:36.227289+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:09:04.448830+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA4 as Amber List (moderate evidence)","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:09:04.435997+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:08:35.149746+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA4: Rating: AMBER; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA4","entity_type":"gene"},{"created":"2020-03-18T11:03:01.263318+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA13 as ready","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:03:01.249240+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa13 has been classified as Red List (Low Evidence).","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:02:47.980135+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA13 were changed from  to Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:02:28.293225+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1731","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA13 were set to ","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:02:12.918851+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1730","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:01:53.692916+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1729","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA13 as Red List (low evidence)","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:01:53.659277+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa13 has been classified as Red List (Low Evidence).","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:01:35.674656+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1728","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA13: Rating: RED; Mode of pathogenicity: None; Publications: 25901006; Phenotypes: Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:00:46.580304+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA13 as ready","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:00:46.570612+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa13 has been classified as Red List (Low Evidence).","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:00:39.971208+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA13 were changed from  to Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T11:00:11.028138+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA13 were set to ","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T10:59:48.861387+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T10:59:21.555145+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA13 as Red List (low evidence)","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T10:59:21.541756+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa13 has been classified as Red List (Low Evidence).","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T10:58:52.023588+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA13: Rating: RED; Mode of pathogenicity: None; Publications: 25901006; Phenotypes: Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA13","entity_type":"gene"},{"created":"2020-03-18T10:53:29.256167+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NADK2 as ready","entity_name":"NADK2","entity_type":"gene"},{"created":"2020-03-18T10:53:29.243181+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nadk2 has been classified as Green List (High Evidence).","entity_name":"NADK2","entity_type":"gene"},{"created":"2020-03-18T10:53:23.722372+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NADK2 as ready","entity_name":"NADK2","entity_type":"gene"},{"created":"2020-03-18T10:53:23.713751+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nadk2 has been classified as Green List (High Evidence).","entity_name":"NADK2","entity_type":"gene"},{"created":"2020-03-18T10:53:15.529318+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NADK2 as Green List (high evidence)","entity_name":"NADK2","entity_type":"gene"},{"created":"2020-03-18T10:53:15.520979+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nadk2 has been classified as Green List (High Evidence).","entity_name":"NADK2","entity_type":"gene"}]}