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{
"count": 220377,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=943",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=941",
"results": [
{
"created": "2022-03-09T19:42:12.878789+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT18 as ready",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:42:12.867134+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt18 has been classified as Red List (Low Evidence).",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:42:04.846612+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT18 were changed from to Cirrhosis, cryptogenic , MIM#215600",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:41:21.000243+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT18 were set to ",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:38:02.732094+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT18 as Red List (low evidence)",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:38:02.716620+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt18 has been classified as Red List (Low Evidence).",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:37:28.856765+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT18: Rating: RED; Mode of pathogenicity: None; Publications: 9011570, 27689336, 20538000; Phenotypes: Cirrhosis, cryptogenic , MIM#215600; Mode of inheritance: None",
"entity_name": "KRT18",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:33:22.144459+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT25 as ready",
"entity_name": "KRT25",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:33:22.134575+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt25 has been classified as Green List (High Evidence).",
"entity_name": "KRT25",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:33:14.242104+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT25 were changed from to Woolly hair, autosomal recessive 3 MIM#616760",
"entity_name": "KRT25",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:32:56.793985+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT25 were set to ",
"entity_name": "KRT25",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:32:36.307892+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KRT25 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "KRT25",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:31:43.790382+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT4 as ready",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:31:43.778812+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt4 has been classified as Green List (High Evidence).",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:31:35.520242+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT4 were changed from to White sponge naevus 1, MIM# 193900",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:28:35.705802+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11239",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT4 were set to ",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:28:13.711447+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KRT4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:27:55.101355+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT4: Rating: GREEN; Mode of pathogenicity: None; Publications: 7493030, 10652003, 12828738; Phenotypes: White sponge naevus 1, MIM# 193900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT4",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:23:52.808243+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT74 as ready",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:23:52.798271+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:15:15.119399+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT74 were changed from to Ectodermal dysplasia 7, hair/nail type MIM#614929; Hypotrichosis 3 , MIM# 613981; Woolly hair, autosomal dominant, MIM# 194300",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:59.095692+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT74 were set to ",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:45.819721+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KRT74 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:26.947973+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT74 as Amber List (moderate evidence)",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:26.931911+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:11.124508+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT74 as ready",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:11.113072+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:09.294125+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT74 were changed from Hypotrichosis 3, 613981 to Hypotrichosis 3 , MIM# 613981; Woolly hair, autosomal dominant, MIM# 194300",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:14:02.533209+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT74 were set to ",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:13:53.509287+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT74 as Amber List (moderate evidence)",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:13:53.497992+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:13:45.820177+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT74: Rating: AMBER; Mode of pathogenicity: None; Publications: 21188418, 20346438, 21188418; Phenotypes: Hypotrichosis 3 , MIM# 613981, Woolly hair, autosomal dominant, MIM# 194300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:13:02.680964+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT74 as ready",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:13:02.657440+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Red List (Low Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:12:56.366783+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT74 as Red List (low evidence)",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:12:56.354073+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Red List (Low Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:12:44.094449+11:00",
"panel_name": "Ectodermal Dysplasia",
"panel_id": 3089,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT74: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ectodermal dysplasia 7, hair/nail type MIM#614929; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:12:19.124981+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT74: Rating: AMBER; Mode of pathogenicity: None; Publications: 24714551, 21188418, 20346438, 21188418; Phenotypes: Ectodermal dysplasia 7, hair/nail type MIM#614929, Hypotrichosis 3 , MIM# 613981, Woolly hair, autosomal dominant, MIM# 194300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:49.083661+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT75 as ready",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:49.069086+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt75 has been classified as Red List (Low Evidence).",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:41.819466+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT75 were changed from to {Pseudofolliculitis barbae, susceptibility to} 612318",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:18.432265+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT75 as Red List (low evidence)",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:18.419995+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt75 has been classified as Red List (Low Evidence).",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:04:00.951144+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT75: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Pseudofolliculitis barbae, susceptibility to} 612318; Mode of inheritance: None",
"entity_name": "KRT75",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:03:08.482982+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT81 as ready",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:03:08.468770+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt81 has been classified as Green List (High Evidence).",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:53.964631+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT81 as ready",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:53.948858+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt81 has been classified as Green List (High Evidence).",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:50.947760+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT81 were changed from Monilethrix, 158000 to Monilethrix, MIM# 158000",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:41.755048+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT81 were set to 31332722",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:22.871540+11:00",
"panel_name": "Hair disorders",
"panel_id": 3269,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT81: Rating: GREEN; Mode of pathogenicity: None; Publications: 9402962, 22628999; Phenotypes: Monilethrix, MIM# 158000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:02:17.317193+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT81 were changed from to Monilethrix, MIM# 158000",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:01:59.196570+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT81 were set to ",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:01:40.969325+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KRT81 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T19:01:22.611130+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT81: Rating: GREEN; Mode of pathogenicity: None; Publications: 9402962, 22628999; Phenotypes: Monilethrix, MIM# 158000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT81",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:02:22.167493+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UNC80 were changed from Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability to Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, MIM# 616801; MONDO:0014777",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:01:56.661635+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UNC80 as Amber List (moderate evidence)",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:01:56.650295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: unc80 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:01:02.423515+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS2 as ready",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:01:02.408914+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars2 has been classified as Green List (High Evidence).",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:00:56.465848+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NARS2 were changed from to Combined oxidative phosphorylation deficiency 24 - MIM#616239; Deafness, autosomal recessive 94 - MIM#618434",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T18:00:13.970608+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NARS2 were set to ",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:59:30.848962+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:58:41.025368+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS2 as ready",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:58:41.013945+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars2 has been classified as Green List (High Evidence).",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:58:32.946498+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NARS2 were changed from to Combined oxidative phosphorylation deficiency 24 - MIM#616239; Deafness, autosomal recessive 94 - MIM#618434",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:58:05.071436+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NARS2 were set to ",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:57:43.521384+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:56:58.732914+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS2 as ready",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:56:58.727776+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Refractory seizures are part of the phenotype.",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:56:58.687564+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars2 has been classified as Green List (High Evidence).",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:56:55.576296+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NARS2 were changed from to Combined oxidative phosphorylation deficiency 24 - MIM#616239",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:56:22.769863+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NARS2 were set to ",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:55:45.887788+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:54:56.986167+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PNPLA3 as ready",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:54:56.972953+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pnpla3 has been classified as Red List (Low Evidence).",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:54:48.025239+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PNPLA3 were changed from to Susceptibility to nonalcoholic fatty liver disease",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:54:26.501929+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PNPLA3 were set to ",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:54:05.296997+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PNPLA3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:53:47.060396+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PNPLA3 as Red List (low evidence)",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:53:47.046520+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pnpla3 has been classified as Red List (Low Evidence).",
"entity_name": "PNPLA3",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:52:32.725599+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS as ready",
"entity_name": "NARS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:52:32.714271+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars has been classified as Green List (High Evidence).",
"entity_name": "NARS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:52:27.309862+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NARS as Green List (high evidence)",
"entity_name": "NARS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:52:27.298777+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars has been classified as Green List (High Evidence).",
"entity_name": "NARS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:51:54.968107+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: NARS.",
"entity_name": "NARS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:51:26.128009+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NANS as ready",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:51:26.116275+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nans has been classified as Green List (High Evidence).",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:50:52.857818+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NANS were changed from to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type - MIM#610442",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:50:19.508449+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4545",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NANS were set to ",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:49:45.568115+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NANS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:48:32.824308+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NANS as ready",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:48:32.814805+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nans has been classified as Green List (High Evidence).",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:48:23.057038+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NANS were changed from to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type - MIM#610442",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:48:02.914808+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NANS were set to ",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T17:47:41.877386+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NANS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-03-09T16:44:37.096328+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.7",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: UNC80: Rating: AMBER; Mode of pathogenicity: None; Publications: 26545877; Phenotypes: Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, MIM# 616801, MONDO:0014777; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-03-09T16:41:42.854382+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: S1PR2 as ready",
"entity_name": "S1PR2",
"entity_type": "gene"
},
{
"created": "2022-03-09T16:41:42.844618+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: s1pr2 has been classified as Green List (High Evidence).",
"entity_name": "S1PR2",
"entity_type": "gene"
},
{
"created": "2022-03-09T16:41:28.554770+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: S1PR2 were changed from to Deafness, autosomal recessive 68, MIM# 610419",
"entity_name": "S1PR2",
"entity_type": "gene"
}
]
}