{"count":221303,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=239","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=237","results":[{"created":"2025-04-30T16:31:24.742448+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.531","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkb has been classified as Green List (High Evidence).","entity_name":"IKBKB","entity_type":"gene"},{"created":"2025-04-30T16:31:22.010039+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.531","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IKBKB were changed from Immunodeficiency 15, 615592 (3) to Immunodeficiency 15, MIM#615592","entity_name":"IKBKB","entity_type":"gene"},{"created":"2025-04-30T16:31:11.095214+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.530","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IKBKB were set to ","entity_name":"IKBKB","entity_type":"gene"},{"created":"2025-04-30T16:30:47.456919+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.529","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IGHMBP2 as ready","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-04-30T16:30:47.449837+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.529","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ighmbp2 has been classified as Green List (High Evidence).","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-04-30T16:30:45.248827+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.529","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IGHMBP2 were changed from Neuronopathy, distal hereditary motor, type VI, 604320 (3) to Neuronopathy, distal hereditary motor, autosomal recessive 1 MIM#604320; Charcot-Marie-Tooth disease, axonal, type 2S MIM#616155","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-04-30T16:30:34.662532+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.528","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IGHMBP2 were set to ","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-04-30T16:30:11.899683+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.527","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDUA as ready","entity_name":"IDUA","entity_type":"gene"},{"created":"2025-04-30T16:30:11.893028+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: idua has been classified as Green List (High Evidence).","entity_name":"IDUA","entity_type":"gene"},{"created":"2025-04-30T16:30:09.636950+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.527","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IDUA were changed from Mucopolysaccharidosis Ih, 607014 (3) to Mucopolysaccharidosis Ih, MIM#607014","entity_name":"IDUA","entity_type":"gene"},{"created":"2025-04-30T16:29:34.795775+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.526","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDS as ready","entity_name":"IDS","entity_type":"gene"},{"created":"2025-04-30T16:29:34.785469+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.526","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ids has been classified as Green List (High Evidence).","entity_name":"IDS","entity_type":"gene"},{"created":"2025-04-30T16:29:32.466204+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.526","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IDS were changed from Mucopolysaccharidosis II, 309900 (3) to Mucopolysaccharidosis II, MIM# 309900; Hunter syndrome, MONDO:0010674","entity_name":"IDS","entity_type":"gene"},{"created":"2025-04-30T16:29:23.511552+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.525","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IDS were set to ","entity_name":"IDS","entity_type":"gene"},{"created":"2025-04-30T16:29:03.652230+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.524","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HYLS1 as ready","entity_name":"HYLS1","entity_type":"gene"},{"created":"2025-04-30T16:29:03.646286+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.524","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hyls1 has been classified as Green List (High Evidence).","entity_name":"HYLS1","entity_type":"gene"},{"created":"2025-04-30T16:29:00.911979+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.524","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HYLS1 were changed from Hydrolethalus syndrome, 236680 (3) to Hydrolethalus syndrome (MIM#236680); Ciliopathy","entity_name":"HYLS1","entity_type":"gene"},{"created":"2025-04-30T16:28:51.696325+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.523","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HYLS1 were set to ","entity_name":"HYLS1","entity_type":"gene"},{"created":"2025-04-30T16:28:29.571249+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.522","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HUWE1 as ready","entity_name":"HUWE1","entity_type":"gene"},{"created":"2025-04-30T16:28:29.565419+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.522","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: huwe1 has been classified as Green List (High Evidence).","entity_name":"HUWE1","entity_type":"gene"},{"created":"2025-04-30T16:28:26.769831+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.522","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HUWE1 were changed from Mental retardation, X-linked syndromic, Turner type, 300706 (3) to Intellectual developmental disorder, X-linked syndromic, Turner type, MIM#309590","entity_name":"HUWE1","entity_type":"gene"},{"created":"2025-04-30T16:28:16.502795+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.521","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HUWE1 were set to ","entity_name":"HUWE1","entity_type":"gene"},{"created":"2025-04-30T16:27:54.943962+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.520","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD3B2 as ready","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2025-04-30T16:27:54.936743+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.520","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd3b2 has been classified as Green List (High Evidence).","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2025-04-30T16:27:52.877856+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.520","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD3B2 were changed from 3-beta-hydroxysteroid dehydrogenase, type II, deficiency, 201810 (3) to Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, MIM#201810","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2025-04-30T16:27:42.449032+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.519","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSD3B2 were set to ","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2025-04-30T16:27:07.196480+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.518","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B4 as ready","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2025-04-30T16:27:07.190121+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.518","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b4 has been classified as Green List (High Evidence).","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2025-04-30T16:27:04.289832+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.518","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B4 were changed from D-bifunctional protein deficiency, 261515 (3) to D-bifunctional protein deficiency, MIM#261515","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2025-04-30T16:26:37.764553+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.517","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B10 as ready","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-04-30T16:26:37.757082+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.517","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b10 has been classified as Green List (High Evidence).","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-04-30T16:26:35.394027+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.517","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B10 were changed from HSD10 mitochondrial disease to HSD10 mitochondrial disease, MIM#300438","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-04-30T16:26:23.091599+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.516","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSD17B10 were set to ","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-04-30T16:26:02.219883+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.515","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPS6 as ready","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-04-30T16:26:02.213150+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.515","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hps6 has been classified as Green List (High Evidence).","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-04-30T16:25:52.357589+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.515","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPS6 were changed from Hermansky-Pudlak syndrome 6, 614075 (3) to Hermansky-Pudlak syndrome 6, MIM# 614075","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-04-30T16:25:43.155101+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.514","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPS6 were set to ","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-04-30T16:25:23.652523+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.513","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPS5 as ready","entity_name":"HPS5","entity_type":"gene"},{"created":"2025-04-30T16:25:23.646219+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.513","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hps5 has been classified as Green List (High Evidence).","entity_name":"HPS5","entity_type":"gene"},{"created":"2025-04-30T16:25:21.156661+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.513","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPS5 were changed from Hermansky-Pudlak syndrome 5, 614074 (3) to Hermansky-Pudlak syndrome 5 MIM#614074","entity_name":"HPS5","entity_type":"gene"},{"created":"2025-04-30T16:25:02.482945+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.512","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPS4 as ready","entity_name":"HPS4","entity_type":"gene"},{"created":"2025-04-30T16:25:02.473248+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hps4 has been classified as Green List (High Evidence).","entity_name":"HPS4","entity_type":"gene"},{"created":"2025-04-30T16:24:49.701759+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.512","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPS4 were changed from Hermansky-Pudlak syndrome 4, 614073 (3) to Hermansky-Pudlak syndrome 4, MIM #614073","entity_name":"HPS4","entity_type":"gene"},{"created":"2025-04-30T16:24:40.213899+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.511","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPS4 were set to ","entity_name":"HPS4","entity_type":"gene"},{"created":"2025-04-30T16:24:22.571203+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.510","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPS3 as ready","entity_name":"HPS3","entity_type":"gene"},{"created":"2025-04-30T16:24:22.561141+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hps3 has been classified as Green List (High Evidence).","entity_name":"HPS3","entity_type":"gene"},{"created":"2025-04-30T16:24:14.702559+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.510","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPS3 were changed from Hermansky-Pudlak syndrome 3, 614072 (3) to Hermansky-Pudlak syndrome 3 MIM#614072","entity_name":"HPS3","entity_type":"gene"},{"created":"2025-04-30T16:24:02.904448+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.509","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPS3 were set to ","entity_name":"HPS3","entity_type":"gene"},{"created":"2025-04-30T16:23:32.753403+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.508","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPS1 as ready","entity_name":"HPS1","entity_type":"gene"},{"created":"2025-04-30T16:23:32.746844+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hps1 has been classified as Green List (High Evidence).","entity_name":"HPS1","entity_type":"gene"},{"created":"2025-04-30T16:23:27.388738+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.508","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPS1 were changed from Hermansky-Pudlak syndrome 1, 203300 (3) to Hermansky-Pudlak syndrome 1, MIM#203300","entity_name":"HPS1","entity_type":"gene"},{"created":"2025-04-30T16:23:15.130999+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.507","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPS1 were set to ","entity_name":"HPS1","entity_type":"gene"},{"created":"2025-04-30T16:22:50.156853+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPRT1 as ready","entity_name":"HPRT1","entity_type":"gene"},{"created":"2025-04-30T16:22:50.150769+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hprt1 has been classified as Green List (High Evidence).","entity_name":"HPRT1","entity_type":"gene"},{"created":"2025-04-30T16:22:44.027471+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.506","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPRT1 were changed from Lesch-Nyhan syndrome, 300322 (3) to Lesch-Nyhan syndrome (MIM#300322)","entity_name":"HPRT1","entity_type":"gene"},{"created":"2025-04-30T16:22:34.807342+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.505","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPRT1 were set to ","entity_name":"HPRT1","entity_type":"gene"},{"created":"2025-04-30T16:22:04.077631+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.504","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPD as ready","entity_name":"HPD","entity_type":"gene"},{"created":"2025-04-30T16:22:04.070740+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hpd has been classified as Green List (High Evidence).","entity_name":"HPD","entity_type":"gene"},{"created":"2025-04-30T16:22:02.025676+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.504","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPD were changed from Tyrosinemia, type III, 276710 (3) to Tyrosinaemia, type III, MIM#276710","entity_name":"HPD","entity_type":"gene"},{"created":"2025-04-30T16:21:46.686398+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.503","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPD were set to ","entity_name":"HPD","entity_type":"gene"},{"created":"2025-04-30T16:21:14.501048+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.502","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HMGCS2 as ready","entity_name":"HMGCS2","entity_type":"gene"},{"created":"2025-04-30T16:21:14.494583+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.502","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hmgcs2 has been classified as Green List (High Evidence).","entity_name":"HMGCS2","entity_type":"gene"},{"created":"2025-04-30T16:21:11.494204+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.502","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HMGCS2 were changed from HMG-CoA synthase-2 deficiency, 605911 (3) to HMG-CoA synthase-2 deficiency, MIM#605911","entity_name":"HMGCS2","entity_type":"gene"},{"created":"2025-04-30T16:20:58.839776+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.501","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HMGCS2 were set to ","entity_name":"HMGCS2","entity_type":"gene"},{"created":"2025-04-30T16:20:35.189535+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.500","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HMGCL as ready","entity_name":"HMGCL","entity_type":"gene"},{"created":"2025-04-30T16:20:35.183165+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.500","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hmgcl has been classified as Green List (High Evidence).","entity_name":"HMGCL","entity_type":"gene"},{"created":"2025-04-30T16:20:32.575112+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.500","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HMGCL were changed from HMG-CoA lyase deficiency, 246450 (3) to HMG-CoA lyase deficiency, MIM# 246450","entity_name":"HMGCL","entity_type":"gene"},{"created":"2025-04-30T16:19:57.658322+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.499","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HLCS as ready","entity_name":"HLCS","entity_type":"gene"},{"created":"2025-04-30T16:19:57.651904+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.499","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hlcs has been classified as Green List (High Evidence).","entity_name":"HLCS","entity_type":"gene"},{"created":"2025-04-30T16:19:55.517268+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.499","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HLCS were changed from Holocarboxylase synthetase deficiency, 253270 (3) to Holocarboxylase synthetase deficiency MIM#253270","entity_name":"HLCS","entity_type":"gene"},{"created":"2025-04-30T16:19:23.321321+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.498","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HIBCH as ready","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-04-30T16:19:23.311587+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.498","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hibch has been classified as Green List (High Evidence).","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-04-30T16:19:20.239470+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.498","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HIBCH were changed from 3-hydroxyisobutryl-CoA hydrolase deficiency, 250620 (3) to 3-hydroxyisobutryl-CoA hydrolase deficiency, MIM#250620","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-04-30T16:19:11.658411+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.497","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HIBCH were set to ","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-04-30T16:18:37.016245+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.496","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HGSNAT as ready","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2025-04-30T16:18:37.006151+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.496","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hgsnat has been classified as Green List (High Evidence).","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2025-04-30T16:18:34.829466+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.496","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HGSNAT were changed from Mucopolysaccharidosis type IIIC (Sanfilippo C), 252930 (3) to Mucopolysaccharidosis type IIIC (Sanfilippo C), MIM#252930; Retinitis pigmentosa 73, MIM#616544","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2025-04-30T16:18:23.065259+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.495","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HGSNAT were set to ","entity_name":"HGSNAT","entity_type":"gene"},{"created":"2025-04-30T16:18:04.141532+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.494","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HFE2 as ready","entity_name":"HFE2","entity_type":"gene"},{"created":"2025-04-30T16:18:04.133808+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hfe2 has been classified as Green List (High Evidence).","entity_name":"HFE2","entity_type":"gene"},{"created":"2025-04-30T16:18:02.307815+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.494","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HFE2 were changed from Hemochromatosis, type 2A, 602390 (3) to Haemochromatosis, type 2A, MIM#602390","entity_name":"HFE2","entity_type":"gene"},{"created":"2025-04-30T16:17:30.737687+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.493","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HEXB as ready","entity_name":"HEXB","entity_type":"gene"},{"created":"2025-04-30T16:17:30.731345+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.493","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexb has been classified as Green List (High Evidence).","entity_name":"HEXB","entity_type":"gene"},{"created":"2025-04-30T16:17:23.780754+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.493","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HEXB were changed from Sandhoff disease, infantile, juvenile, and adult forms, 268800 (3) to Sandhoff disease, infantile, juvenile, and adult forms, MIM#268800","entity_name":"HEXB","entity_type":"gene"},{"created":"2025-04-30T16:17:14.304697+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.492","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HEXB were set to ","entity_name":"HEXB","entity_type":"gene"},{"created":"2025-04-30T16:16:55.032081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.491","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HEXA as ready","entity_name":"HEXA","entity_type":"gene"},{"created":"2025-04-30T16:16:55.020595+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexa has been classified as Green List (High Evidence).","entity_name":"HEXA","entity_type":"gene"},{"created":"2025-04-30T16:16:53.087921+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.491","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HEXA were changed from Tay-Sachs disease, 272800 (3) to Tay-Sachs disease, MIM#272800","entity_name":"HEXA","entity_type":"gene"},{"created":"2025-04-30T16:16:37.294592+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.490","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HEXA were set to ","entity_name":"HEXA","entity_type":"gene"},{"created":"2025-04-30T16:16:16.759884+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.489","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCFC1 as ready","entity_name":"HCFC1","entity_type":"gene"},{"created":"2025-04-30T16:16:16.749468+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.489","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcfc1 has been classified as Green List (High Evidence).","entity_name":"HCFC1","entity_type":"gene"},{"created":"2025-04-30T16:16:14.896213+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.489","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCFC1 were changed from Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ), 309541 (3) to Methylmalonic aciduria and homocysteinemia, cblX type, MIM#309541","entity_name":"HCFC1","entity_type":"gene"},{"created":"2025-04-30T16:15:59.409209+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.488","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCFC1 were set to ","entity_name":"HCFC1","entity_type":"gene"},{"created":"2025-04-30T16:15:35.793885+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.487","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HBB as ready","entity_name":"HBB","entity_type":"gene"},{"created":"2025-04-30T16:15:35.787349+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.487","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hbb has been classified as Green List (High Evidence).","entity_name":"HBB","entity_type":"gene"},{"created":"2025-04-30T16:15:34.022058+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.487","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HBB were changed from Thalassemias, beta-, 613985 (3) to Sickle cell anaemia, MIM# 603903","entity_name":"HBB","entity_type":"gene"},{"created":"2025-04-30T16:15:04.446917+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HAX1 as ready","entity_name":"HAX1","entity_type":"gene"},{"created":"2025-04-30T16:15:04.436640+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hax1 has been classified as Green List (High Evidence).","entity_name":"HAX1","entity_type":"gene"},{"created":"2025-04-30T16:15:02.637081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAX1 were changed from Neutropenia, severe congenital 3, autosomal recessive, 610738 (3) to Neutropenia, severe congenital 3, autosomal recessive, MIM#610738","entity_name":"HAX1","entity_type":"gene"},{"created":"2025-04-30T16:14:49.736964+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.485","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HAX1 were set to ","entity_name":"HAX1","entity_type":"gene"}]}