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{
"count": 220451,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1525",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1523",
"results": [
{
"created": "2020-10-25T20:34:52.573542+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apopt1 has been classified as Green List (High Evidence).",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:34:49.093723+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: APOPT1 were changed from to Mitochondrial complex IV deficiency, nuclear type 17, MIM#619061",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:34:45.248773+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: APOPT1 were changed from to Mitochondrial complex IV deficiency, nuclear type 17, MIM#619061",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:34:25.732852+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: APOPT1 were set to ",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:34:20.635259+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.543",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: APOPT1 were set to 25175347",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:34:00.096547+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: APOPT1 were set to 25175347]",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:33:43.637456+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: APOPT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:33:40.588738+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: APOPT1 were set to 25175347]",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:33:13.605214+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: APOPT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25175347]; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 17, MIM#619061; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:33:05.043567+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.541",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: APOPT1 were set to ",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:32:46.035846+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: APOPT1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:32:27.431282+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: APOPT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:31:59.348752+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: APOPT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25175347]; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 17, MIM#619061; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APOPT1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:29:33.200593+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX4I1 as ready",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:29:33.185117+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:29:27.982296+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX4I1 as Amber List (moderate evidence)",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:29:27.972122+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:28:59.809385+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COX4I1 was added\ngene: COX4I1 was added to Regression. Sources: Expert list\nMode of inheritance for gene: COX4I1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COX4I1 were set to 28766551; 22592081; 31290619\nPhenotypes for gene: COX4I1 were set to Mitochondrial complex IV deficiency, nuclear type 16, MIM#619060\nReview for gene: COX4I1 was set to AMBER\nAdded comment: Two unrelated families reported, regression was a feature in both. \nSources: Expert list",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:28:22.456065+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX4I1 as ready",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:28:22.445632+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:28:05.784746+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX4I1 as Amber List (moderate evidence)",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:28:05.776155+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:27:11.768166+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COX4I1 was added\ngene: COX4I1 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: COX4I1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COX4I1 were set to 28766551; 22592081; 31290619\nPhenotypes for gene: COX4I1 were set to Mitochondrial complex IV deficiency, nuclear type 16, MIM#619060\nReview for gene: COX4I1 was set to AMBER\nAdded comment: Two unrelated families reported.\r\n\r\nTwo more variants reported in PMID: 22592081: one is non-coding and the other rare missense, appear to have been identified in separate individuals, i.e. heterozygous in each individual. \nSources: Expert list",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:26:42.569712+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX4I1 were changed from short stature; mild dysmorphic features; Fanconi anemia to Mitochondrial complex IV deficiency, nuclear type 16, MIM#619060; regression; seizures; short stature; mild dysmorphic features; Fanconi anemia",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:26:17.581928+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX4I1 were set to 28766551; 22592081",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:25:04.995487+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX4I1 as Amber List (moderate evidence)",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:25:04.987716+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:24:35.295372+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX4I1: Added comment: Further family with two affected sibs reported in PMID 31290619, upgrade to Amber.; Changed rating: AMBER; Changed publications: 28766551, 22592081, 31290619; Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 16, MIM#619060",
"entity_name": "COX4I1",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:22:43.148250+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX8A were changed from Mitochondrial complex IV deficiency, MIM# 220110 to Mitochondrial complex IV deficiency, nuclear type 15, MIM#619059",
"entity_name": "COX8A",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:22:24.599213+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX8A: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 15, MIM#619059",
"entity_name": "COX8A",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:22:05.562300+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX8A were changed from Mitochondrial complex IV deficiency, MIM# 220110 to Mitochondrial complex IV deficiency, nuclear type 15, MIM#619059",
"entity_name": "COX8A",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:21:33.924780+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX8A: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 15, MIM#619059",
"entity_name": "COX8A",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:20:55.329309+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COA3 were changed from Mitochondrial complex IV deficiency to Mitochondrial complex IV deficiency, nuclear type 14, MIM# 619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:20:24.076129+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COA3: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 14, MIM# 619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:20:07.237391+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COA3 were changed from Mitochondrial complex IV deficiency to Mitochondrial complex IV deficiency, nuclear type 14, MIM# 619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:19:49.113488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COA3: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 14, MIM# 619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:19:40.321598+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COA3 were changed from Mitochondrial complex IV deficiency to Mitochondrial complex IV deficiency, nuclear type 14, MIM#619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:19:03.384066+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COA3: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 14, MIM# 619058",
"entity_name": "COA3",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:18:06.671143+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PET100 as ready",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:18:06.660365+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pet100 has been classified as Red List (Low Evidence).",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:18:00.477158+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PET100 were changed from to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:17:41.531803+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PET100 were set to 24462369; 25293719; 31406627",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:17:22.178441+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PET100 were set to ",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:17:00.231804+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PET100 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:15:57.535602+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PET100 as Red List (low evidence)",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:15:57.528279+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pet100 has been classified as Red List (Low Evidence).",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:15:29.744148+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PET100: Rating: RED; Mode of pathogenicity: None; Publications: 24462369, 25293719, 31406627; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:14:14.693269+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.893",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PET100 as ready",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:14:14.681298+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.893",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pet100 has been classified as Green List (High Evidence).",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:14:11.870367+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.893",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PET100 were changed from to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:13:42.902163+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.892",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PET100 were set to ",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:13:15.223980+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.891",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PET100 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:12:46.661673+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.890",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: PET100.",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:12:37.420943+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.890",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PET100: Rating: GREEN; Mode of pathogenicity: None; Publications: 24462369, 25293719, 31406627; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:11:31.661290+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PET100 were changed from Mitochondrial complex IV deficiency, MIM# 220110 to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:11:01.919940+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: PET100.",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:10:46.225041+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PET100: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:10:26.207226+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PET100 as ready",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:10:26.189700+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pet100 has been classified as Green List (High Evidence).",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:10:13.900275+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PET100 were changed from to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:09:53.685126+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PET100 were set to ",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:09:35.667149+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PET100 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:09:19.170073+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: PET100.",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:09:07.830317+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PET100: Rating: GREEN; Mode of pathogenicity: None; Publications: 24462369, 25293719, 31406627; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:08:45.687553+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PET100 as ready",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:08:45.675085+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pet100 has been classified as Green List (High Evidence).",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:08:23.194760+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PET100 were changed from to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:07:31.900460+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PET100 were set to ",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:07:03.488911+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PET100 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:06:36.787567+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: PET100.",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:06:28.273344+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PET100: Rating: GREEN; Mode of pathogenicity: None; Publications: 24462369, 25293719, 31406627; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PET100",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:02:01.369304+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX20 as ready",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:02:01.347171+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox20 has been classified as Green List (High Evidence).",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:01:54.470493+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX20 were changed from to Mitochondrial complex IV deficiency, nuclear type 11, MIM#619054",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:01:32.290832+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX20 were set to ",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:01:14.428295+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COX20 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:00:56.404956+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX20: Rating: GREEN; Mode of pathogenicity: None; Publications: 24202787, 31079202, 30656193, 23125284, 32606554; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 11, MIM#619054; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:00:30.319715+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX20 as ready",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:00:30.307532+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox20 has been classified as Green List (High Evidence).",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T20:00:23.396507+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX20 were changed from to Mitochondrial complex IV deficiency, nuclear type 11, MIM#619054",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:59:50.367388+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX20 were set to ",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:59:21.121861+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COX20 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:58:51.925748+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX20: Rating: GREEN; Mode of pathogenicity: None; Publications: 24202787, 31079202, 30656193, 23125284, 32606554; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 11, MIM#619054; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:49:12.621238+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX14 as ready",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:49:12.611075+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox14 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:49:07.751466+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from ?Mitochondrial complex IV deficiency, 220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM# 619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:48:48.853857+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX14 were set to ",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:48:34.602253+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX14 as Amber List (moderate evidence)",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:48:34.594387+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox14 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:48:24.881689+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX14: Rating: AMBER; Mode of pathogenicity: None; Publications: 22243966; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM# 619053; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:47:36.076248+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from Mitochondrial complex IV deficiency, MIM#220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:47:02.566774+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX14: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:46:39.789940+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from Mitochondrial complex IV deficiency, MIM#220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:46:09.616031+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX14: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:45:51.767497+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from Mitochondrial complex IV deficiency, MIM#220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:45:29.530870+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX14: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:45:06.995610+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from Mitochondrial complex IV deficiency, MIM#220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM#\t619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:44:31.760851+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: COX14: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM# 619053",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:43:20.342490+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TACO1 as ready",
"entity_name": "TACO1",
"entity_type": "gene"
},
{
"created": "2020-10-25T19:43:20.334346+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taco1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TACO1",
"entity_type": "gene"
}
]
}