HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=854",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=852",
"results": [
{
"created": "2022-05-05T20:13:42.313494+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP7B1 as ready",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:13:42.302376+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp7b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:13:18.416022+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP7B1 were changed from to Bile acid synthesis defect, congenital, 3 MIM#613812; Spastic paraplegia 5A, autosomal recessive MIM#270800; Disorders of bile acid biosynthesis",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:12:48.338832+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP7B1 were set to ",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:12:26.853864+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP7B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:52.670101+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CYP1A2 as ready",
"entity_name": "CYP1A2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:52.658811+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyp1a2 has been classified as Red List (Low Evidence).",
"entity_name": "CYP1A2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:44.234429+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Classified gene: CYP1A2 as Red List (low evidence)",
"entity_name": "CYP1A2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:44.223014+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyp1a2 has been classified as Red List (Low Evidence).",
"entity_name": "CYP1A2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:28.695234+10:00",
"panel_name": "Palmoplantar Keratoderma and Erythrokeratoderma",
"panel_id": 153,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KLF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KLF4",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:09:26.688370+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13835",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CYP1A2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes",
"entity_name": "CYP1A2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:08:42.607180+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KLF4 as ready",
"entity_name": "KLF4",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:08:42.596196+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: klf4 has been classified as Green List (High Evidence).",
"entity_name": "KLF4",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:08:30.059754+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KLF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KLF4",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:48.273241+10:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFV2 as ready",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:48.261473+10:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufv2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:38.379933+10:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFV2 as Green List (high evidence)",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:38.368709+10:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufv2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:27.327865+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13834",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CYP19A1 as ready",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:27.317279+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13834",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyp19a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:17.488574+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13834",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: CYP19A1.",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:16.456170+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13834",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYP19A1 were changed from to Aromatase deficiency (MIM#613546), AR; Aromatase excess syndrome (MIM#139300), AD",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:09.697090+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13833",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CYP19A1 were set to ",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:07:05.449143+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13833",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP19A1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:06:55.959715+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: P3H2 as ready",
"entity_name": "P3H2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:06:55.948037+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: p3h2 has been classified as Green List (High Evidence).",
"entity_name": "P3H2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:06:49.598181+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: P3H2 as Green List (high evidence)",
"entity_name": "P3H2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:06:49.587454+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: p3h2 has been classified as Green List (High Evidence).",
"entity_name": "P3H2",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:06:44.545163+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13832",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CYP19A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17164303, 25264451; Phenotypes: Aromatase deficiency (MIM#613546), AR, Aromatase excess syndrome (MIM#139300), AD; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:04:27.859835+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13832",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CYCS as ready",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:04:27.849795+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13832",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cycs has been classified as Green List (High Evidence).",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:04:15.083847+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13832",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYCS were changed from to Thrombocytopenia 4, MIM# 612004",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:04:11.049618+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13831",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CYCS were set to ",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:04:05.132226+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13831",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYCS was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:03:36.288762+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13830",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CYCS: Rating: GREEN; Mode of pathogenicity: None; Publications: 24326104, 18345000, 30051457; Phenotypes: Thrombocytopenia 4, MIM# 612004; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CYCS",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:03:35.271781+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4751",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYC1 were changed from Mitochondrial complex III deficiency, nuclear type 6 MIM#615453 to Mitochondrial complex III deficiency, nuclear type 6 MIM#615453",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:03:17.188695+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "1.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TULP3 as ready",
"entity_name": "TULP3",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:03:17.175756+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "1.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tulp3 has been classified as Green List (High Evidence).",
"entity_name": "TULP3",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:03:13.531982+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4749",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYC1 were changed from Mitochondrial complex III deficiency, nuclear type 6 MIM#615453 to Mitochondrial complex III deficiency, nuclear type 6 MIM#615453",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:02:50.805562+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4750",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYC1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:02:40.282432+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4750",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CYC1 as ready",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:02:40.243668+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4750",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyc1 has been classified as Red List (Low Evidence).",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:02:21.614543+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRG1 were changed from Hirschsprung disease to Hirschsprung disease, MONDO:0018309; Peripheral neuropathy MONDO:0005244",
"entity_name": "NRG1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:02:18.988837+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4750",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYC1 were changed from to Mitochondrial complex III deficiency, nuclear type 6 MIM#615453",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:01:58.654916+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4750",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CYC1 were set to 23910460; 34252606",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:01:34.291904+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4749",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CYC1 were set to ",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:01:03.530904+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4749",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:00:59.197499+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NRG1 as Amber List (moderate evidence)",
"entity_name": "NRG1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:00:59.186347+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nrg1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NRG1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:00:40.821779+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4749",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Classified gene: CYC1 as Red List (low evidence)",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T20:00:40.804723+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4749",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyc1 has been classified as Red List (Low Evidence).",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:59:51.689846+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "1.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRAPPC9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Intellectual developmental disorder, autosomal recessive 13, MIM# 613192; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:59:50.845130+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4748",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CYC1: Rating: RED; Mode of pathogenicity: None; Publications: 23910460, 34252606; Phenotypes: Mitochondrial complex III deficiency, nuclear type 6 MIM#615453; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:57:44.910735+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13828",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CYC1 as ready",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:57:44.888623+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13828",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cyc1 has been classified as Green List (High Evidence).",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:57:15.391197+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTR9 were changed from Neurodevelopmental disorder (MONDO:0700092), CTR9 related; Intellectual disability (MONDO:0001071); hypotonia (HP:0001252); joint hyperlaxity (HP:0001388); speech delay; coordination problems; tremor (HP:0001337); autism spectrum disorder (MONDO:0005258) to Neurodevelopmental disorder (MONDO:0700092), CTR9 related",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:57:03.420571+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13827",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CYC1 were set to ",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:57:02.990325+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13828",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CYC1 were changed from to Mitochondrial complex III deficiency, nuclear type 6 MIM#615453",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:56:52.472888+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13827",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:56:36.829055+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTR9 as ready",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:56:36.817157+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctr9 has been classified as Green List (High Evidence).",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:56:11.535814+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13826",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CYC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23910460, 34252606; Phenotypes: Mitochondrial complex III deficiency, nuclear type 6 MIM#615453; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:56:11.183660+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTR9 were changed from Neurodevelopmental disorder (MONDO:0700092), CTR9-related; Intellectual disability (MONDO:0001071); hypotonia (HP:0001252); joint hyperlaxity (HP:0001388); speech delay; coordination problems; tremor (HP:0001337); autism spectrum disorder (MONDO:0005258) to Neurodevelopmental disorder (MONDO:0700092), CTR9-related",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:55:31.584828+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CTR9 as Green List (high evidence)",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:55:31.575311+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctr9 has been classified as Green List (High Evidence).",
"entity_name": "CTR9",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:53:17.945926+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAH14 as Green List (high evidence)",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:53:17.936866+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah14 has been classified as Green List (High Evidence).",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:52:41.830995+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH14 were changed from Neurodevelopmental disorder, DNAH14-related (MONDO#0700092) to Neurodevelopmental disorder (MONDO#0700092), DNAH14-related",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:52:40.737511+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAH14 as ready",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:52:40.722691+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah14 has been removed from the panel.",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:52:27.743955+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH14 were changed from Neurodevelopmental disorder, DNAH14-related (MONDO#0700092) to Neurodevelopmental disorder (MONDO#0700092), DNAH14-related",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:51:30.497258+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAH14 as ready",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:51:30.484232+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah14 has been classified as Green List (High Evidence).",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:51:22.305042+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH14 were changed from Neurodevelopmental disorder, DNAH14-related (MONDO#0700092) to Neurodevelopmental disorder (MONDO#0700092), DNAH14-related",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:50:10.353494+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1590",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAH14 as Green List (high evidence)",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:50:10.343498+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1590",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah14 has been classified as Green List (High Evidence).",
"entity_name": "DNAH14",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:48:32.605777+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HNRNPA2B1 were changed from Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 MIM#615422 to oculopharyngeal muscular dystrophy, MONDO:0008116; Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 MIM#615422",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:58.078707+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPA2B1 as Green List (high evidence)",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:58.065049+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpa2b1 has been classified as Green List (High Evidence).",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:32.269298+10:00",
"panel_name": "Congenital ophthalmoplegia",
"panel_id": 3379,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HNRNPA2B1 as ready",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:32.257839+10:00",
"panel_name": "Congenital ophthalmoplegia",
"panel_id": 3379,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpa2b1 has been classified as Green List (High Evidence).",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:25.583800+10:00",
"panel_name": "Congenital ophthalmoplegia",
"panel_id": 3379,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPA2B1 as Green List (high evidence)",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:47:25.574517+10:00",
"panel_name": "Congenital ophthalmoplegia",
"panel_id": 3379,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpa2b1 has been classified as Green List (High Evidence).",
"entity_name": "HNRNPA2B1",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:03:53.287035+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DTYMK as ready",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:03:53.274619+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dtymk has been classified as Green List (High Evidence).",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:03:41.042542+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DTYMK as Green List (high evidence)",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:03:41.030951+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dtymk has been classified as Green List (High Evidence).",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:02:19.006752+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DTYMK as ready",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:02:18.995104+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dtymk has been classified as Green List (High Evidence).",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:02:13.280659+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DTYMK as Green List (high evidence)",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:02:13.271743+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dtymk has been classified as Green List (High Evidence).",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:01:43.220610+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DTYMK was added\ngene: DTYMK was added to Regression. Sources: Expert Review\nMode of inheritance for gene: DTYMK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DTYMK were set to 34918187; 31271740\nPhenotypes for gene: DTYMK were set to Neurodegeneration, childhood-onset, with progressive microcephaly (MIM# 619847)\nReview for gene: DTYMK was set to GREEN\nAdded comment: Progressive neurodegenerative disorder, 3 families reported. \nSources: Expert Review",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T19:00:11.743783+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DTYMK were changed from Intellectual disability; microcephaly to Neurodegeneration, childhood-onset, with progressive microcephaly (MIM# 619847)",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:59:23.983707+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13822",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DTYMK were set to 31271740",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:59:01.877539+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DTYMK as Green List (high evidence)",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:59:01.863290+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dtymk has been classified as Green List (High Evidence).",
"entity_name": "DTYMK",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:58:07.837281+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRDM13 were changed from intellectual disability, MONDO:0001071, PRDM13-associated; ataxia with cerebellar hypoplasia, MONDO:0016054, PRDM13-associated; congenital hypogonadotropic hypogonadism, MONDO:0015770 to intellectual disability, MONDO:0001071, PRDM13-associated; Pontocerebellar hypoplasia (MONDO:0020135), PRDM13 related; congenital hypogonadotropic hypogonadism, MONDO:0015770",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:57:34.514909+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRDM13 were set to 34730112",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:56:58.739744+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRDM13 as Green List (high evidence)",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2022-05-05T18:56:58.728000+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm13 has been classified as Green List (High Evidence).",
"entity_name": "PRDM13",
"entity_type": "gene"
}
]
}