{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=244","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=242","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"}]}