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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1902",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}