HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1877",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1875",
"results": [
{
"created": "2020-04-07T19:53:47.976804+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.101",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: ZAP70: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Autoimmune disease, multisystem, infantile-onset, 2 MIM#617006, Immunodeficiency 48 MIM#269840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2020-04-07T13:45:16.110798+10:00",
"panel_name": "Usher Syndrome",
"panel_id": 3086,
"panel_version": "0.6",
"user_name": "Chern Lim",
"item_type": "entity",
"text": "reviewed gene: USH2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 26927203, 22135276; Phenotypes: Retinitis pigmentosa 39, MIM#613809, Usher syndrome, type 2A, MIM#276901; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "USH2A",
"entity_type": "gene"
},
{
"created": "2020-04-07T12:24:56.077758+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.25",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; KidGen; Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-04-07T11:28:05.545617+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2033",
"user_name": "Kristin Rigbye",
"item_type": "entity",
"text": "reviewed gene: KCNT2: Rating: GREEN; Mode of pathogenicity: Other; Publications: 29069600, 29740868, 32038177; Phenotypes: Epileptic encephalopathy, early infantile, 57, 617771, Epilepsy of infancy with migrating focal seizures (EIMFS); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNT2",
"entity_type": "gene"
},
{
"created": "2020-04-07T10:46:45.826554+10:00",
"panel_name": "Limb Girdle Muscular Dystrophy",
"panel_id": 3071,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-04-06T20:20:09.907412+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.101",
"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": "2020-04-06T20:17:19.021579+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BTK as ready",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:17:19.012631+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: btk has been classified as Red List (Low Evidence).",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:17:12.115617+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BTK were changed from to X-linked agammaglobulinemia; isolated growth hormone deficiency type III with agammaglobulinemia",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:16:48.288681+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BTK was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:16:21.144406+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BTK as Red List (low evidence)",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:16:21.119829+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: btk has been classified as Red List (Low Evidence).",
"entity_name": "BTK",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:15:36.790231+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HPS1 as ready",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:15:36.776655+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:15:33.833458+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HPS1 were changed from to Hermansky-Pudlak syndrome 1 (203300)",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:15:11.552294+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HPS1 were set to ",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:14:42.417459+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HPS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:14:14.705762+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HPS1 as Amber List (moderate evidence)",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:14:14.696657+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:13:24.351586+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HPS4 as ready",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:13:24.338183+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:13:21.012377+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HPS4 were changed from to Hermansky-Pudlak syndrome 4 (614073)",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:12:57.482543+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HPS4 were set to ",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:12:33.624868+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HPS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:12:11.327672+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HPS4 as Amber List (moderate evidence)",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:12:11.314482+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:11:21.595508+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HPS6 as ready",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:11:21.587108+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:11:18.218876+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HPS6 were changed from to Hermansky-Pudlak syndrome 6 (614075)",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:10:54.918240+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HPS6 were set to ",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:10:32.069785+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HPS6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:10:10.239062+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HPS6 as Amber List (moderate evidence)",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:10:10.230921+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hps6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:09:10.700969+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HTRA2 as ready",
"entity_name": "HTRA2",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:09:10.691848+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: htra2 has been classified as Green List (High Evidence).",
"entity_name": "HTRA2",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:09:05.694209+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HTRA2 as Green List (high evidence)",
"entity_name": "HTRA2",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:09:05.681096+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: htra2 has been classified as Green List (High Evidence).",
"entity_name": "HTRA2",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:08:08.134735+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ICOS as ready",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:08:08.121336+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: icos has been classified as Red List (Low Evidence).",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:08:04.597514+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ICOS were changed from to Common variable immunodeficiency 1 (604558)",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:07:41.488691+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ICOS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:07:15.245875+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ICOS as Red List (low evidence)",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:07:15.233193+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: icos has been classified as Red List (Low Evidence).",
"entity_name": "ICOS",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:06:28.842682+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IKBKG as ready",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:06:28.828673+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ikbkg has been classified as Amber List (Moderate Evidence).",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:06:25.249849+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IKBKG were changed from to Incontinentia pigmenti (308300); / Ectodermal dysplasia and immunodeficiency 1 (300291); Ectodermal dysplasia, anhidrotic, lymphoedema and immunodeficiency (300301); Immunodeficiency 33 (300636); Immunodeficiency, isolated (300584); Invasive pneumococcal disease, recurrent isolated 2 (300640)",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:06:02.003366+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IKBKG were set to ",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:05:24.328813+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IKBKG was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:04:54.660194+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IKBKG as Amber List (moderate evidence)",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:04:54.646933+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ikbkg has been classified as Amber List (Moderate Evidence).",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:58.704962+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL10 as ready",
"entity_name": "IL10",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:58.696072+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10 has been classified as Red List (Low Evidence).",
"entity_name": "IL10",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:54.064640+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL10 as Red List (low evidence)",
"entity_name": "IL10",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:54.050874+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10 has been classified as Red List (Low Evidence).",
"entity_name": "IL10",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:00.345092+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL10RA as ready",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:03:00.336844+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10ra has been classified as Red List (Low Evidence).",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:02:56.687454+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL10RA were changed from to Inflammatory bowel disease 28, early onset (613148)",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:02:33.533799+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL10RA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:02:10.786125+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL10RA as Red List (low evidence)",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T20:02:10.777204+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10ra has been classified as Red List (Low Evidence).",
"entity_name": "IL10RA",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:57:28.292251+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIEZO1 as ready",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:57:28.283430+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: piezo1 has been classified as Green List (High Evidence).",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:57:17.333128+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIEZO1 were set to ",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:56:32.980537+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIEZO1 were changed from to Lymphatic malformation 6, 616843; Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema, 194380",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:56:18.594086+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: PIEZO1 was changed from to Other",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:56:01.099364+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIEZO1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:54:49.928119+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX19 as ready",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:54:49.919592+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx19 has been classified as Green List (High Evidence).",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:54:41.619456+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX19 were changed from to Adrenocorticotropic hormone deficiency, 201400",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:54:24.186668+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX19 were set to ",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:54:01.760578+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:52:42.472784+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL10RB as ready",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:52:42.456534+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10rb has been classified as Red List (Low Evidence).",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:52:39.465264+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL10RB were changed from to Inflammatory bowel disease 25, early onset (612567)",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:51:55.350018+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL10RB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:51:32.739160+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL10RB as Red List (low evidence)",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:51:32.726351+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il10rb has been classified as Red List (Low Evidence).",
"entity_name": "IL10RB",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:50:38.415830+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL2RG as ready",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:50:38.402267+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il2rg has been classified as Red List (Low Evidence).",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:50:35.645754+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL2RG were changed from to Severe combined immunodeficiency, X-linked (300400); Moderate combined immunodeficiency, X-linked (312863)",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:50:11.649228+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL2RG was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:49:37.259287+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL2RG as Red List (low evidence)",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:49:37.250972+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il2rg has been classified as Red List (Low Evidence).",
"entity_name": "IL2RG",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:48:23.241460+10:00",
"panel_name": "Porphyria",
"panel_id": 3077,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Panel name changed from Porphyria_RMH to Porphyria\nPanel status changed from internal to public\nPanel types changed to Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-04-06T19:47:49.868258+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCF20 as ready",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:47:49.854882+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcf20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:47:46.919879+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCF20 were changed from to Developmental delay with variable intellectual impairment and behavioral abnormalities, AD, MIM#618430",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:47:17.372127+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCF20 were set to ",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:46:49.374058+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCF20 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:45:41.686307+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TCF20 as Amber List (moderate evidence)",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:45:41.673118+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcf20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:45:13.108660+10:00",
"panel_name": "Overgrowth",
"panel_id": 151,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TCF20: Rating: AMBER; Mode of pathogenicity: None; Publications: 30739909, 30819258, 25228304; Phenotypes: Developmental delay with variable intellectual impairment and behavioral abnormalities, AD, MIM#618430; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:43:24.090442+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCF20 as ready",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:43:24.077014+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcf20 has been classified as Green List (High Evidence).",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:41:03.818256+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.57",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: XK as ready",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:41:03.808847+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.57",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: xk has been classified as Green List (High Evidence).",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:40:57.054775+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.57",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: XK as Green List (high evidence)",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:40:57.046193+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.57",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: xk has been classified as Green List (High Evidence).",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:40:44.045951+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.56",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: XK was added\ngene: XK was added to Dystonia - complex. Sources: Expert list\nMode of inheritance for gene: XK was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPublications for gene: XK were set to 11761473\nPhenotypes for gene: XK were set to McLeod syndrome with or without chronic granulomatous disease MIM#300842\nReview for gene: XK was set to GREEN\nAdded comment: 5 out of 13 cases had dystonia as a feature of the condition. \nSources: Expert list",
"entity_name": "XK",
"entity_type": "gene"
},
{
"created": "2020-04-06T19:25:33.379937+10:00",
"panel_name": "Dystonia - complex",
"panel_id": 290,
"panel_version": "0.55",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: VPS37A was added\ngene: VPS37A was added to Dystonia - complex. Sources: Expert list\nMode of inheritance for gene: VPS37A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS37A were set to 22717650\nPhenotypes for gene: VPS37A were set to Spastic paraplegia 53, autosomal recessive MIM#614898\nReview for gene: VPS37A was set to RED\nAdded comment: Single consanguineous Arab Moslem kindred with dystonia as a feature of the condition. \nSources: Expert list",
"entity_name": "VPS37A",
"entity_type": "gene"
}
]
}