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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1309",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1307",
"results": [
{
"created": "2021-06-05T17:13:26.224683+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE3B were set to ",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:13:00.956008+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBE3B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:12:27.660617+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBE3B: Rating: GREEN; Mode of pathogenicity: None; Publications: 23200864, 23200864, 34012380, 32949109; Phenotypes: Kaufman oculocerebrofacial syndrome, MIM# 244450, MONDO:0009485; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:11:46.535659+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBE3B as ready",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:11:46.525540+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ube3b has been classified as Green List (High Evidence).",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:11:44.182274+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBE3B were changed from to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:11:14.497476+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE3B were set to ",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:10:49.828386+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBE3B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T17:10:26.447605+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBE3B: Rating: GREEN; Mode of pathogenicity: None; Publications: 23200864, 23200864, 34012380, 32949109; Phenotypes: Kaufman oculocerebrofacial syndrome, MIM# 244450, MONDO:0009485; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:04:33.123121+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: KANSL1.",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:04:18.706714+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KANSL1 as ready",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:04:18.691330+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kansl1 has been classified as Green List (High Evidence).",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:04:16.149198+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KANSL1 were changed from to Koolen-De Vries syndrome, MIM# 610443; MONDO:0012496",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:03:46.845598+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KANSL1 were set to ",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:03:24.510258+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KANSL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:02:53.719946+10:00",
"panel_name": "Angelman Rett like syndromes",
"panel_id": 41,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KANSL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19447831, 22544367, 22544363; Phenotypes: Koolen-De Vries syndrome, MIM# 610443, MONDO:0012496; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:01:45.754504+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KANSL1 as ready",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:01:45.740115+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kansl1 has been classified as Green List (High Evidence).",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:01:42.182583+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: KANSL1.",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:01:34.663500+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KANSL1 were changed from Koolen-De Vries syndrome, MIM# 610443 to Koolen-De Vries syndrome, MIM# 610443; MONDO:0012496",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:00:53.888930+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KANSL1 were changed from to Koolen-De Vries syndrome, MIM# 610443",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T15:00:30.513127+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KANSL1 were set to ",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:59:53.417004+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KANSL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:59:24.062771+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KANSL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19447831, 22544367, 22544363; Phenotypes: Koolen-De Vries syndrome, MIM# 610443; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KANSL1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:51:14.423348+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HUWE1 as ready",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:51:14.412648+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: huwe1 has been classified as Green List (High Evidence).",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:51:11.757102+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HUWE1 were changed from to Mental retardation, X-linked syndromic, Turner type, MIM# 309590; MONDO:0010407",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:50:48.880746+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HUWE1 were set to ",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:50:18.201888+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HUWE1 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:49:53.109592+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HUWE1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:49:29.955757+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HUWE1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18252223, 29180823; Phenotypes: Mental retardation, X-linked syndromic, Turner type, MIM# 309590, MONDO:0010407; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "HUWE1",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:46:21.964479+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSPG2 as ready",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:46:21.955149+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspg2 has been classified as Green List (High Evidence).",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:46:19.528228+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSPG2 were changed from to Schwartz-Jampel syndrome, type 1, MIM# 255800; MONDO:0009717",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:45:54.722492+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.273",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSPG2 were set to ",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:45:28.028580+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSPG2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:45:04.400991+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HSPG2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11101850, 16927315; Phenotypes: Schwartz-Jampel syndrome, type 1, MIM# 255800, MONDO:0009717; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:43:51.361770+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7851",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSPG2 were set to 16927315",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:43:26.334224+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HSPG2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11101850, 16927315, 11279527; Phenotypes: Schwartz-Jampel syndrome, type 1, MIM# 255800, MONDO:0009717, Dyssegmental dysplasia, Silverman-Handmaker type, MIM# 224410, MONDO:0009140; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:39:53.015206+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSPG2 as ready",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:39:52.991855+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspg2 has been classified as Green List (High Evidence).",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:39:49.163699+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSPG2 were changed from to Schwartz-Jampel syndrome, type 1, MIM# 255800; MONDO:0009717",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:39:21.542262+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSPG2 were set to ",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:38:54.517371+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSPG2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T14:38:29.412522+10:00",
"panel_name": "Blepharophimosis",
"panel_id": 55,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HSPG2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11101850, 16927315; Phenotypes: Schwartz-Jampel syndrome, type 1, MIM# 255800, MONDO:0009717; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPG2",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:40:35.980336+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HLA-DRB1 as ready",
"entity_name": "HLA-DRB1",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:40:35.969847+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-drb1 has been classified as Red List (Low Evidence).",
"entity_name": "HLA-DRB1",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:40:27.416259+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HLA-DRB1 as Red List (low evidence)",
"entity_name": "HLA-DRB1",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:40:27.405374+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-drb1 has been classified as Red List (Low Evidence).",
"entity_name": "HLA-DRB1",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:40:09.590702+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HLA-DRB1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HLA-DRB1",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:39:39.547513+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HLA-DRA as ready",
"entity_name": "HLA-DRA",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:39:39.538166+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-dra has been classified as Red List (Low Evidence).",
"entity_name": "HLA-DRA",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:39:31.667233+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HLA-DRA as Red List (low evidence)",
"entity_name": "HLA-DRA",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:39:31.655528+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-dra has been classified as Red List (Low Evidence).",
"entity_name": "HLA-DRA",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:39:16.497176+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HLA-DRA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HLA-DRA",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:38:44.197309+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HLA-C as ready",
"entity_name": "HLA-C",
"entity_type": "gene"
},
{
"created": "2021-06-05T12:38:44.183050+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-c has been classified as Red List (Low Evidence).",
"entity_name": "HLA-C",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:29:05.106888+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HLA-C as Red List (low evidence)",
"entity_name": "HLA-C",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:29:05.097083+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-c has been classified as Red List (Low Evidence).",
"entity_name": "HLA-C",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:28:44.467501+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HLA-C: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HLA-C",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:28:18.853294+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HLA-B as ready",
"entity_name": "HLA-B",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:28:18.843178+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-b has been classified as Red List (Low Evidence).",
"entity_name": "HLA-B",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:28:09.868500+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HLA-B as Red List (low evidence)",
"entity_name": "HLA-B",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:28:09.858174+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-b has been classified as Red List (Low Evidence).",
"entity_name": "HLA-B",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:27:52.260352+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HLA-B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HLA-B",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:27:21.911053+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HLA-A as ready",
"entity_name": "HLA-A",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:27:21.901321+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-a has been classified as Red List (Low Evidence).",
"entity_name": "HLA-A",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:27:13.055974+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HLA-A as Red List (low evidence)",
"entity_name": "HLA-A",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:27:13.045748+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hla-a has been classified as Red List (Low Evidence).",
"entity_name": "HLA-A",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:26:56.609957+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7845",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HLA-A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HLA-A",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:26:17.792927+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7845",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAF6 as ready",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:26:17.782986+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7845",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taf6 has been classified as Green List (High Evidence).",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:26:05.357930+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7845",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAF6 were changed from to Alazami-Yuan syndrome, MIM# 617126",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:25:39.287665+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7844",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAF6 were set to ",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:24:16.142347+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAF6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:23:54.922970+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7842",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAF6: Rating: GREEN; Mode of pathogenicity: None; Publications: 25558065, 25574841, 32030742; Phenotypes: Alazami-Yuan syndrome, MIM# 617126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:22:04.036763+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAF6 as ready",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:22:04.026626+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taf6 has been classified as Green List (High Evidence).",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:21:59.177562+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAF6 were changed from Alazami-Yuan syndrome, MIM# 617126 to Alazami-Yuan syndrome, MIM# 617126",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:21:44.141069+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAF6 were changed from to Alazami-Yuan syndrome, MIM# 617126",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:21:13.833359+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAF6 were set to ",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:20:52.136588+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAF6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:19:00.873334+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAF6: Rating: GREEN; Mode of pathogenicity: None; Publications: 25558065, 25574841, 32030742; Phenotypes: Alazami-Yuan syndrome, MIM# 617126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAF6",
"entity_type": "gene"
},
{
"created": "2021-06-05T11:00:03.303942+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7842",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ANGPT2 were changed from Primary lymphoedema to Lymphatic malformation-10, MIM#619369; Primary lymphoedema",
"entity_name": "ANGPT2",
"entity_type": "gene"
},
{
"created": "2021-06-05T10:59:43.642408+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ANGPT2: Changed phenotypes: Lymphatic malformation-10, MIM#619369, Primary lymphoedema",
"entity_name": "ANGPT2",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:07:28.084646+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-06-04T20:07:08.995595+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-06-04T20:06:26.046503+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC24A5 as ready",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:06:26.035332+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc24a5 has been classified as Green List (High Evidence).",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:06:13.999233+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC24A5 were changed from to Albinism, oculocutaneous, type VI, MIM# 113750",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:55.875590+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC24A5 were set to ",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:41.336930+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC24A5 as ready",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:41.326713+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc24a5 has been classified as Green List (High Evidence).",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:36.767096+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC24A5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:19.943842+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC24A5 were changed from to Albinism, oculocutaneous, type VI, MIM# 113750",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:05:17.523402+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC24A5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23364476, 23985994, 26491832; Phenotypes: Albinism, oculocutaneous, type VI, MIM# 113750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:04:33.302659+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC24A5 were set to ",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:04:09.953574+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC24A5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:03:26.264817+10:00",
"panel_name": "Ocular and Oculocutaneous Albinism",
"panel_id": 37,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC24A5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23364476, 23985994, 26491832; Phenotypes: Albinism, oculocutaneous, type VI, MIM# 113750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2021-06-04T20:01:05.732321+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC45A2 as ready",
"entity_name": "SLC45A2",
"entity_type": "gene"
}
]
}