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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=244",
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"results": [
{
"created": "2025-04-30T14:48:18.666058+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.293",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLD as ready",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:48:18.658114+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.293",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dld has been classified as Green List (High Evidence).",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:48:16.815326+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.293",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLD were changed from Dihydrolipoamide dehydrogenase deficiency, 246900 (3) to Dihydrolipoamide dehydrogenase deficiency (MIM#246900)",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:48:08.352026+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLD were set to ",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:52.850573+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DKC1 as ready",
"entity_name": "DKC1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:52.843789+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dkc1 has been classified as Green List (High Evidence).",
"entity_name": "DKC1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:50.729243+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DKC1 were changed from Dyskeratosis congenita, X-linked, 305000 (3) to Dyskeratosis congenita, X-linked MIM#305000",
"entity_name": "DKC1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:28.417037+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.290",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DKC1 were set to ",
"entity_name": "DKC1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:08.717234+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.289",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DIS3L2 as ready",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:08.710665+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.289",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dis3l2 has been classified as Green List (High Evidence).",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:47:05.762677+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.289",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DIS3L2 were changed from Perlman syndrome, 267000 (3) to Perlman syndrome MIM# 267000",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:56.615135+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DIS3L2 were set to ",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:33.104288+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.287",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DHDDS as ready",
"entity_name": "DHDDS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:33.096243+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.287",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dhdds has been classified as Green List (High Evidence).",
"entity_name": "DHDDS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:30.994955+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.287",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DHDDS were changed from Retinitis pigmentosa 59, 613861 (3) to Retinitis pigmentosa 59, MIM#613861; Congenital disorder of glycosylation, type 1bb, MIM# 613861",
"entity_name": "DHDDS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:15.197799+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.286",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DHDDS were set to ",
"entity_name": "DHDDS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:00.181956+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.285",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DHCR7 as ready",
"entity_name": "DHCR7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:46:00.175275+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.285",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dhcr7 has been classified as Green List (High Evidence).",
"entity_name": "DHCR7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:56.273852+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.285",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DHCR7 were changed from Smith-Lemli-Opitz syndrome, 270400 (3) to Smith-Lemli-Opitz syndrome (MIM#270400)",
"entity_name": "DHCR7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:46.628182+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DHCR7 were set to ",
"entity_name": "DHCR7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:28.957308+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DHCR24 as ready",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:28.946342+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dhcr24 has been classified as Green List (High Evidence).",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:26.738740+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DHCR24 were changed from Desmosterolosis, 602398 (3) to Desmosterolosis, MIM#602398",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:17.802167+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DHCR24 were set to ",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:01.736203+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DGUOK as ready",
"entity_name": "DGUOK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:45:01.729553+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dguok has been classified as Green List (High Evidence).",
"entity_name": "DGUOK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:57.920946+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DGUOK were changed from Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 (3) to Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), MIM# 251880; Portal hypertension, noncirrhotic, 1, MIM# 617068; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4, MIM# 617070",
"entity_name": "DGUOK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:41.601031+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DGUOK were set to ",
"entity_name": "DGUOK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:14.043068+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DGAT1 as ready",
"entity_name": "DGAT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:14.033731+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dgat1 has been classified as Green List (High Evidence).",
"entity_name": "DGAT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:11.452116+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DGAT1 were changed from ?Diarrhea 7, protein-losing enteropathy type to Diarrhoea 7, protein-losing enteropathy type, MIM# 615863; congenital diarrhea 7 with exudative enteropathy MONDO:0014375",
"entity_name": "DGAT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:44:01.784991+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.278",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DGAT1 were set to ",
"entity_name": "DGAT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:44.850519+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.277",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDX11 as ready",
"entity_name": "DDX11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:44.840876+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.277",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddx11 has been classified as Green List (High Evidence).",
"entity_name": "DDX11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:42.316602+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.277",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDX11 were changed from Warsaw breakage syndrome, 613398 (3) to Warsaw breakage syndrome MIM#613398",
"entity_name": "DDX11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:33.098243+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.276",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDX11 were set to ",
"entity_name": "DDX11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:15.150685+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDC as ready",
"entity_name": "DDC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:15.144269+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddc has been classified as Green List (High Evidence).",
"entity_name": "DDC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:43:12.450124+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDC were changed from Aromatic L-amino acid decarboxylase deficiency, 608643 (3) to Aromatic L-amino acid decarboxylase deficiency MIM#608643; Aromatic L-amino acid decarboxylase deficiency (MIM#608643)",
"entity_name": "DDC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:42:26.757335+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DCX as ready",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:42:26.750388+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dcx has been classified as Green List (High Evidence).",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:42:15.050209+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DCX were changed from Lissencephaly, X-linked, 300067 (3) to Lissencephaly, X-linked MIM#300067; Subcortical laminal heterotopia, X-linked MIM#300067",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:42:05.450232+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.273",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DCX were set to ",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:41:36.591155+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DCLRE1C as ready",
"entity_name": "DCLRE1C",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:41:36.585048+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dclre1c has been classified as Green List (High Evidence).",
"entity_name": "DCLRE1C",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:41:34.662258+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DCLRE1C were changed from Severe combined immunodeficiency, Athabascan type, 602450 (3) to Severe combined immunodeficiency, Athabascan type, MIM# 602450; Omenn syndrome, MIM# 603554",
"entity_name": "DCLRE1C",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:41:19.029597+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DCLRE1C were set to ",
"entity_name": "DCLRE1C",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:45.404648+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DCAF17 as ready",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:45.394917+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dcaf17 has been classified as Green List (High Evidence).",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:43.234380+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DCAF17 were changed from Woodhouse-Sakati syndrome, 241080 (3) to Woodhouse-Sakati syndrome MIM#241080",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:34.741021+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DCAF17 were set to ",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:18.717539+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DBT as ready",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:18.711442+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dbt has been classified as Green List (High Evidence).",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:40:16.326962+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DBT were changed from Maple syrup urine disease, type II, 248600 (3) to Maple syrup urine disease, type II, MIM#248600",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:58.218391+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: D2HGDH as ready",
"entity_name": "D2HGDH",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:58.210825+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: d2hgdh has been classified as Green List (High Evidence).",
"entity_name": "D2HGDH",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:55.937392+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: D2HGDH were changed from D-2-hydroxyglutaric aciduria, 600721 (3) to D-2-hydroxyglutaric aciduria, MIM#600721",
"entity_name": "D2HGDH",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:47.600166+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: D2HGDH were set to ",
"entity_name": "D2HGDH",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:28.172904+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP7B1 as ready",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:28.166676+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp7b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:39:25.322295+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP7B1 were changed from Bile acid synthesis defect, congenital, 3, 613812 (3) to Bile acid synthesis defect, congenital, 3, MIM#613812; Spastic paraplegia 5A, MIM#270800",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:59.529391+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP7B1 were set to ",
"entity_name": "CYP7B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:43.237529+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP27A1 as ready",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:43.230534+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp27a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:41.174048+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP27A1 were changed from Cerebrotendinous xanthomatosis, 213700 (3) to Cerebrotendinous xanthomatosis, MIM#213700",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:06.319209+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP1B1 as ready",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:06.312484+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp1b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:38:01.408921+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP1B1 were changed from Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3) to Anterior segment dysgenesis 6, multiple subtypes, MIM#617315",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:37:47.537258+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP1B1 were set to ",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:37:30.102936+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP17A1 as ready",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:37:30.095948+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp17a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:37:28.024410+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP17A1 were changed from 17,20-lyase deficiency, isolated, 202110 (3) to 17-alpha-hydroxylase/17,20-lyase deficiency MIM#202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:37:18.626381+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP17A1 were set to ",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:49.729449+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.258",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11B2 as ready",
"entity_name": "CYP11B2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:49.722894+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.258",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11b2 has been classified as Green List (High Evidence).",
"entity_name": "CYP11B2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:47.379551+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.258",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11B2 were changed from Hypoaldosteronism, congenital, due to CMO I deficiency, 203400 (3) to Hypoaldosteronism, congenital, due to CMO I deficiency MIM#203400; Hypoaldosteronism, congenital, due to CMO II deficiency MIM#610600",
"entity_name": "CYP11B2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:34.454971+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11B2 were set to ",
"entity_name": "CYP11B2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:18.905763+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11A1 as ready",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:18.895941+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:36:16.794937+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11A1 were changed from Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3) to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete MIM#613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:35:52.504609+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11A1 were set to ",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:35:17.614906+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYBB: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chronic granulomatous disease, X-linked, MIM#306400; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:35:02.185384+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYBB as ready",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:35:02.175393+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cybb has been classified as Green List (High Evidence).",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:34:36.405010+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYBB were changed from Chronic granulomatous disease, X-linked, 306400 (3) to Chronic granulomatous disease, X-linked, MIM#306400",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:34:17.716468+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYBB were set to ",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:51.809627+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYBA as ready",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:51.802018+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyba has been classified as Green List (High Evidence).",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:49.944673+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYBA were changed from Chronic granulomatous disease, autosomal, due to deficiency of CYBA, 233690 (3) to Chronic granulomatous disease 4 MIM#233690",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:40.850466+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYBA were set to ",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:16.517537+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CUL4B as ready",
"entity_name": "CUL4B",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:16.510849+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cul4b has been classified as Green List (High Evidence).",
"entity_name": "CUL4B",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:12.310703+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CUL4B were changed from Mental retardation, X-linked, syndromic 15 (Cabezas type), 300354 (3) to Intellectual developmental disorder, X-linked syndromic, Cabezas type, MIM#300354",
"entity_name": "CUL4B",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:33:02.478299+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CUL4B were set to ",
"entity_name": "CUL4B",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:47.294538+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTSK as ready",
"entity_name": "CTSK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:47.285290+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsk has been classified as Green List (High Evidence).",
"entity_name": "CTSK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:45.295871+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTSK were changed from Pycnodysostosis, 265800 (3) to Pycnodysostosis MIM#265800",
"entity_name": "CTSK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:36.859472+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTSK were set to ",
"entity_name": "CTSK",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:15.218714+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTSD as ready",
"entity_name": "CTSD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:32:15.212519+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsd has been classified as Green List (High Evidence).",
"entity_name": "CTSD",
"entity_type": "gene"
}
]
}