{"count":221277,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=228","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=226","results":[{"created":"2025-05-09T16:35:45.634570+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGM1 as ready","entity_name":"PGM1","entity_type":"gene"},{"created":"2025-05-09T16:35:45.626861+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgm1 has been classified as Green List (High Evidence).","entity_name":"PGM1","entity_type":"gene"},{"created":"2025-05-09T16:35:43.895176+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PGM1 were changed from Congenital disorder of glycosylation, type It, 614921 (3) to Congenital disorder of glycosylation, type It (MIM#614921)","entity_name":"PGM1","entity_type":"gene"},{"created":"2025-05-09T16:35:34.294229+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.793","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PGM1 were set to ","entity_name":"PGM1","entity_type":"gene"},{"created":"2025-05-09T16:35:14.902485+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGK1 as ready","entity_name":"PGK1","entity_type":"gene"},{"created":"2025-05-09T16:35:14.895210+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgk1 has been classified as Green List (High Evidence).","entity_name":"PGK1","entity_type":"gene"},{"created":"2025-05-09T16:35:12.474387+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PGK1 were changed from Phosphoglycerate kinase 1 deficiency, 300653 (3) to Phosphoglycerate kinase 1 deficiency (MIM#300653)","entity_name":"PGK1","entity_type":"gene"},{"created":"2025-05-09T16:34:48.343509+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.791","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGAP2 as ready","entity_name":"PGAP2","entity_type":"gene"},{"created":"2025-05-09T16:34:48.333177+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.791","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgap2 has been classified as Green List (High Evidence).","entity_name":"PGAP2","entity_type":"gene"},{"created":"2025-05-09T16:34:46.102817+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.791","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PGAP2 were changed from Hyperphosphatasia with mental retardation syndrome 3, 614207 (3) to Hyperphosphatasia with impaired intellectual development syndrome 3, MIM#614207","entity_name":"PGAP2","entity_type":"gene"},{"created":"2025-05-09T16:34:36.297019+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.790","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PGAP2 were set to ","entity_name":"PGAP2","entity_type":"gene"},{"created":"2025-05-09T16:34:15.567763+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.789","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PFKM as ready","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-05-09T16:34:15.560568+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.789","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pfkm has been classified as Green List (High Evidence).","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-05-09T16:34:13.502935+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.789","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PFKM were changed from Glycogen storage disease VII, 232800 (3) to Glycogen storage disease VII MIM#232800","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-05-09T16:34:04.640435+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.788","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PFKM were set to ","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-05-09T16:33:44.359675+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.787","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX7 as ready","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-05-09T16:33:44.350144+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.787","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex7 has been classified as Green List (High Evidence).","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-05-09T16:33:42.041714+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.787","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX7 were changed from Chondrodysplasia punctata, rhizomelic, type 1, 215100 (3) to Peroxisome biogenesis disorder 9B, MIM# 614879; Rhizomelic chondrodysplasia punctata, type 1, MIM# 215100","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-05-09T16:33:32.483244+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.786","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX7 were set to ","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-05-09T16:32:55.580589+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.785","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX6 as ready","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-05-09T16:32:55.570844+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.785","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex6 has been classified as Green List (High Evidence).","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-05-09T16:32:53.572966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.785","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX6 were changed from Peroxisome biogenesis disorder 4A (Zellweger), 614862 to Peroxisome biogenesis disorder 4A (Zellweger), MIM# 614862; Peroxisome biogenesis disorder-4B, MIM# 614863","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-05-09T16:32:44.191346+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.784","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX6 were set to ","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-05-09T16:13:54.305115+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.783","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX5 as ready","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-05-09T16:13:54.295164+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.783","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex5 has been classified as Green List (High Evidence).","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-05-09T16:13:51.679719+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.783","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX5 were changed from Peroxisome biogenesis disorder 2A (Zellweger), 214110 to Peroxisome biogenesis disorder 2A (Zellweger), MIM#214110","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-05-09T16:13:43.271764+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.782","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX5 were set to ","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-05-09T16:13:22.328606+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.781","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX26 as ready","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-05-09T16:13:22.321476+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.781","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex26 has been classified as Green List (High Evidence).","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-05-09T16:13:20.072518+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.781","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX26 were changed from Peroxisome biogenesis disorder 7A (Zellweger), 614872 to Peroxisome biogenesis disorder 7A (Zellweger) - MIM#614872, MONDO:0013938; Peroxisome biogenesis disorder 7B - MIM#614873, MONDO:0013939","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-05-09T16:13:09.474786+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.780","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX26 were set to ","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-05-09T16:12:48.469073+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.779","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX2 as ready","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-05-09T16:12:48.459516+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.779","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex2 has been classified as Green List (High Evidence).","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-05-09T16:12:46.421891+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.779","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX2 were changed from Peroxisome biogenesis disorder 5A (Zellweger), 614866 to Peroxisome biogenesis disorder 5A (Zellweger), MIM#614866; Peroxisome biogenesis disorder 5B, MIM#614867","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-05-09T16:12:36.743284+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.778","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX2 were set to ","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-05-09T16:12:16.087341+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.777","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX16 as ready","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-05-09T16:12:16.077790+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.777","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex16 has been classified as Green List (High Evidence).","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-05-09T16:12:14.404824+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.777","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX16 were changed from Peroxisome biogenesis disorder 8A, (Zellweger), 614876 to Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876; Peroxisome biogenesis disorder 8B MIM#614877","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-05-09T16:12:04.514057+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.776","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX16 were set to ","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-05-09T16:11:39.806886+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.775","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX13 as ready","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-05-09T16:11:39.800160+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.775","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Green List (High Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-05-09T16:11:36.755929+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.775","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX13 were changed from Peroxisome biogenesis disorder 11A (Zellweger), 614883 to Peroxisome biogenesis disorder 11A (Zellweger), MIM#614883; Peroxisome biogenesis disorder 11B, MIM#614885","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-05-09T16:10:17.957125+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.774","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX12 as ready","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-05-09T16:10:17.945089+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.774","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex12 has been classified as Green List (High Evidence).","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-05-09T16:10:15.736601+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.774","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX12 were changed from Peroxisome biogenesis disorder 3A (Zellweger), 614859 to Peroxisome biogenesis disorder 3A (Zellweger), MIM#614859; Peroxisome biogenesis disorder 3B, MIM#266510","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-05-09T16:09:55.258321+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.773","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX10 as ready","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-05-09T16:09:55.248860+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.773","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex10 has been classified as Green List (High Evidence).","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-05-09T16:09:53.038865+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.773","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX10 were changed from Peroxisome biogenesis disorder 6A (Zellweger), 614870 to Peroxisome biogenesis disorder 6A (Zellweger) MIM#614870; Peroxisome biogenesis disorder 6B MIM#614871","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-05-09T16:09:42.324043+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.772","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX10 were set to ","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-05-09T16:09:21.534888+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.771","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX1 as ready","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-05-09T16:09:21.528021+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.771","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-05-09T16:09:18.593085+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.771","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX1 were changed from Peroxisome biogenesis disorder 1A (Zellweger), 214100 to Peroxisome biogenesis disorder 1A (Zellweger), MIM #214100; Heimler syndrome 1, MIM #234580; Peroxisome biogenesis disorder 1B (NALD/IRD), MIM #601539; MONDO:0100259","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-05-09T16:09:07.881452+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.770","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX1 were set to ","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-05-09T16:07:20.600047+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.769","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PET100 as ready","entity_name":"PET100","entity_type":"gene"},{"created":"2025-05-09T16:07:20.590441+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.769","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pet100 has been classified as Green List (High Evidence).","entity_name":"PET100","entity_type":"gene"},{"created":"2025-05-09T16:07:17.625388+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.769","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PET100 were changed from Mitochondrial complex IV deficiency, 220110 (3) to Mitochondrial complex IV deficiency, nuclear type 12, MIM# 619055","entity_name":"PET100","entity_type":"gene"},{"created":"2025-05-09T16:06:55.983397+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.768","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEPD as ready","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-05-09T16:06:55.976745+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.768","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pepd has been classified as Green List (High Evidence).","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-05-09T16:06:53.537035+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.768","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEPD were changed from Prolidase deficiency, 170100 (3) to Prolidase deficiency, MIM# 170100","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-05-09T16:06:44.772059+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.767","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEPD were set to ","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-05-09T16:06:24.687035+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.766","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDHB as ready","entity_name":"PDHB","entity_type":"gene"},{"created":"2025-05-09T16:06:24.679687+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdhb has been classified as Green List (High Evidence).","entity_name":"PDHB","entity_type":"gene"},{"created":"2025-05-09T16:06:21.855101+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.766","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDHB were changed from Pyruvate dehydrogenase E1-beta deficiency, 614111 (3) to Pyruvate dehydrogenase E1-beta deficiency, MIM #614111","entity_name":"PDHB","entity_type":"gene"},{"created":"2025-05-09T16:06:12.623647+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.765","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDHB were set to ","entity_name":"PDHB","entity_type":"gene"},{"created":"2025-05-09T16:01:51.908913+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.764","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDHA1 as ready","entity_name":"PDHA1","entity_type":"gene"},{"created":"2025-05-09T16:01:51.899081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.764","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdha1 has been classified as Green List (High Evidence).","entity_name":"PDHA1","entity_type":"gene"},{"created":"2025-05-09T16:01:14.852269+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.764","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCNT as ready","entity_name":"PCNT","entity_type":"gene"},{"created":"2025-05-09T16:01:14.845760+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.764","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcnt has been classified as Green List (High Evidence).","entity_name":"PCNT","entity_type":"gene"},{"created":"2025-05-09T16:01:12.209152+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.764","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II, 210720 (3) to Microcephalic osteodysplastic primordial dwarfism, type II, MIM# 210720; MONDO:0008872","entity_name":"PCNT","entity_type":"gene"},{"created":"2025-05-09T16:01:01.528747+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.763","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCNT were set to ","entity_name":"PCNT","entity_type":"gene"},{"created":"2025-05-09T16:00:26.912671+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Severe condition meets criteria for screening. Note it needs special filtering.; to: Severe condition meets criteria for screening. Note it needs special filtering to detect male carriers at risk of having affected female children.","entity_name":"PCDH19","entity_type":"gene"},{"created":"2025-05-09T15:59:35.205157+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCDH19 as ready","entity_name":"PCDH19","entity_type":"gene"},{"created":"2025-05-09T15:59:35.197315+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcdh19 has been classified as Green List (High Evidence).","entity_name":"PCDH19","entity_type":"gene"},{"created":"2025-05-09T15:58:51.924341+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCDH15 as ready","entity_name":"PCDH15","entity_type":"gene"},{"created":"2025-05-09T15:58:51.914823+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcdh15 has been classified as Green List (High Evidence).","entity_name":"PCDH15","entity_type":"gene"},{"created":"2025-05-09T15:58:49.283712+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.762","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCDH15 were changed from Usher syndrome, type 1F, 602083 (3) to Usher syndrome, type 1F, MIM# 602083","entity_name":"PCDH15","entity_type":"gene"},{"created":"2025-05-09T15:58:39.937692+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.761","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCDH15 were set to ","entity_name":"PCDH15","entity_type":"gene"},{"created":"2025-05-09T15:58:20.065034+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.760","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCCB as ready","entity_name":"PCCB","entity_type":"gene"},{"created":"2025-05-09T15:58:20.054371+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pccb has been classified as Green List (High Evidence).","entity_name":"PCCB","entity_type":"gene"},{"created":"2025-05-09T15:58:17.915473+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.760","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCCB were changed from Propionicacidemia, 606054 (3) to Propionicacidemia MIM#606054; propionic acidemia MONDO:0011628","entity_name":"PCCB","entity_type":"gene"},{"created":"2025-05-09T15:58:07.769698+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.759","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCCB were set to ","entity_name":"PCCB","entity_type":"gene"},{"created":"2025-05-09T15:57:46.433559+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.758","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCCA as ready","entity_name":"PCCA","entity_type":"gene"},{"created":"2025-05-09T15:57:46.423634+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.758","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcca has been classified as Green List (High Evidence).","entity_name":"PCCA","entity_type":"gene"},{"created":"2025-05-09T15:57:44.212337+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.758","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCCA were changed from Propionicacidemia, MIM#606054 to Propionicacidaemia, MIM#606054","entity_name":"PCCA","entity_type":"gene"},{"created":"2025-05-09T15:57:36.864086+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.757","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCCA were changed from Propionicacidemia, 606054 (3) to Propionicacidemia, MIM#606054","entity_name":"PCCA","entity_type":"gene"},{"created":"2025-05-09T15:57:27.389963+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.756","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCCA were set to ","entity_name":"PCCA","entity_type":"gene"},{"created":"2025-05-09T15:57:04.742632+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.755","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PC as ready","entity_name":"PC","entity_type":"gene"},{"created":"2025-05-09T15:57:04.733072+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.755","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pc has been classified as Green List (High Evidence).","entity_name":"PC","entity_type":"gene"},{"created":"2025-05-09T15:57:02.814569+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.755","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PC were changed from Pyruvate carboxylase deficiency, 266150 (3) to Pyruvate carboxylase deficiency (MIM#266150)","entity_name":"PC","entity_type":"gene"},{"created":"2025-05-09T15:56:53.054016+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.754","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PC were set to ","entity_name":"PC","entity_type":"gene"},{"created":"2025-05-09T15:56:31.861298+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.753","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PANK2 as ready","entity_name":"PANK2","entity_type":"gene"},{"created":"2025-05-09T15:56:31.851117+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.753","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pank2 has been classified as Green List (High Evidence).","entity_name":"PANK2","entity_type":"gene"},{"created":"2025-05-09T15:56:29.269332+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.753","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PANK2 were changed from Neurodegeneration with brain iron accumulation 1, MIM#234200 to HARP syndrome (MIM#607236); Neurodegeneration with brain iron accumulation 1 (MIM#234200)","entity_name":"PANK2","entity_type":"gene"},{"created":"2025-05-09T15:56:04.093340+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.752","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAK3 as ready","entity_name":"PAK3","entity_type":"gene"},{"created":"2025-05-09T15:56:04.083289+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.752","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pak3 has been classified as Green List (High Evidence).","entity_name":"PAK3","entity_type":"gene"},{"created":"2025-05-09T15:56:01.470457+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.752","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAK3 were changed from Mental retardation, X-linked 30/47, 300558 (3) to Intellectual developmental disorder, X-linked 30 MIM#300558","entity_name":"PAK3","entity_type":"gene"},{"created":"2025-05-09T15:55:52.105132+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.751","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAK3 were set to ","entity_name":"PAK3","entity_type":"gene"},{"created":"2025-05-09T15:55:30.973669+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.750","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAH as ready","entity_name":"PAH","entity_type":"gene"},{"created":"2025-05-09T15:55:30.966292+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.750","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pah has been classified as Green List (High Evidence).","entity_name":"PAH","entity_type":"gene"},{"created":"2025-05-09T15:55:28.866038+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.750","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAH were changed from Phenylketonuria,MIM#261600 to Phenylketonuria, MIM#261600","entity_name":"PAH","entity_type":"gene"}]}