{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=243","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=241","results":[{"created":"2025-04-30T15:04:01.804876+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.343","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC2 were set to ","entity_name":"ERCC2","entity_type":"gene"},{"created":"2025-04-30T15:03:41.738333+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.342","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPG5 as ready","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-04-30T15:03:41.731959+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epg5 has been classified as Green List (High Evidence).","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-04-30T15:03:24.443437+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.342","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPG5 were changed from Vici syndrome, 242840 (3) to Vici syndrome MIM# 242840","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-04-30T15:03:12.882569+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.341","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPG5 were set to ","entity_name":"EPG5","entity_type":"gene"},{"created":"2025-04-30T15:02:49.057576+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.340","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ENPP1 as ready","entity_name":"ENPP1","entity_type":"gene"},{"created":"2025-04-30T15:02:49.047958+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.340","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: enpp1 has been classified as Green List (High Evidence).","entity_name":"ENPP1","entity_type":"gene"},{"created":"2025-04-30T15:02:46.816636+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.340","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ENPP1 were changed from Hypophosphatemic rickets, autosomal recessive, 2, 613312 (3) to Arterial calcification, generalized, of infancy, 1 MIM#208000; Hypophosphatemic rickets, autosomal recessive, 2 MIM#613312","entity_name":"ENPP1","entity_type":"gene"},{"created":"2025-04-30T15:02:37.086571+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.339","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ENPP1 were set to ","entity_name":"ENPP1","entity_type":"gene"},{"created":"2025-04-30T15:02:07.813023+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.338","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMD as ready","entity_name":"EMD","entity_type":"gene"},{"created":"2025-04-30T15:02:07.806202+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.338","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emd has been classified as Green List (High Evidence).","entity_name":"EMD","entity_type":"gene"},{"created":"2025-04-30T15:01:51.729158+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.338","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EMD were changed from Emery-Dreifuss muscular dystrophy 1, X-linked, 310300 (3) to Emery-Dreifuss muscular dystrophy 1, X-linked, MIM# 310300","entity_name":"EMD","entity_type":"gene"},{"created":"2025-04-30T15:01:35.514150+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.337","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EMD were set to ","entity_name":"EMD","entity_type":"gene"},{"created":"2025-04-30T15:01:13.446534+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.336","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ELP1 as ready","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-04-30T15:01:13.440343+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.336","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: elp1 has been classified as Green List (High Evidence).","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-04-30T15:01:11.261106+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.336","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ELP1 were changed from Dysautonomia, familial, 223900 (3) to Dysautonomia, familial MIM#223900","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-04-30T15:00:55.970245+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.335","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ELP1 were set to ","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-04-30T15:00:35.630398+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.334","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B5 as ready","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2025-04-30T15:00:35.624390+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b5 has been classified as Green List (High Evidence).","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2025-04-30T15:00:33.772347+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.334","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B5 were changed from Leukoencephalopathy with vanishing white matter, 603896 (3) to Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure (MIM#620315)","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2025-04-30T15:00:23.896713+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.333","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2B5 were set to ","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2025-04-30T15:00:02.887359+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.332","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B4 as ready","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2025-04-30T15:00:02.877352+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.332","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b4 has been classified as Green List (High Evidence).","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2025-04-30T15:00:00.797114+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.332","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B4 were changed from Leukoencephaly with vanishing white matter, 603896 (3) to Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure MIM#620314","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2025-04-30T14:59:46.743877+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.331","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2B4 were set to ","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2025-04-30T14:59:12.464047+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.330","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B3 as ready","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2025-04-30T14:59:12.457486+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.330","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b3 has been classified as Green List (High Evidence).","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2025-04-30T14:59:10.215125+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.330","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B3 were changed from Leukoencephalopathy with vanishing white matter, 603896 (3) to Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure MIM#620313","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2025-04-30T14:59:00.526291+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.329","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2B3 were set to ","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2025-04-30T14:58:38.798281+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.328","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B2 as ready","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2025-04-30T14:58:38.791815+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.328","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b2 has been classified as Green List (High Evidence).","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2025-04-30T14:58:32.992518+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.328","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B2 were changed from Leukoencephalopathy with vanishing white matter, 603896 (3) to Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure, MIM #620312","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2025-04-30T14:58:23.770986+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.327","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2B2 were set to ","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2025-04-30T14:58:04.160164+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.326","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B1 as ready","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2025-04-30T14:58:04.153401+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.326","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b1 has been classified as Green List (High Evidence).","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2025-04-30T14:58:02.174289+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.326","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B1 were changed from Leukoencephalopathy with vanishing white matter, 603896 (3) to Leukoencephalopathy with vanishing white matter 1, with or without ovarian failure MIM#603896","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2025-04-30T14:57:52.562801+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.325","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2B1 were set to ","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2025-04-30T14:57:32.773451+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.324","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2AK3 as ready","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2025-04-30T14:57:32.766943+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.324","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2ak3 has been classified as Green List (High Evidence).","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2025-04-30T14:57:09.832287+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.324","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2AK3 were changed from Wolcott-Rallison syndrome, 226980 (3) to Wolcott-Rallison syndrome MIM#226980","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2025-04-30T14:57:00.223966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.323","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2AK3 were set to ","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2025-04-30T14:56:25.622635+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.322","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDA as ready","entity_name":"EDA","entity_type":"gene"},{"created":"2025-04-30T14:56:25.615534+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.322","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eda has been classified as Green List (High Evidence).","entity_name":"EDA","entity_type":"gene"},{"created":"2025-04-30T14:56:23.657964+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.322","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EDA were changed from Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3) to Ectodermal dysplasia 1, hypohidrotic, X-linked MIM#305100; Tooth agenesis, selective, X-linked 1 MIM#313500","entity_name":"EDA","entity_type":"gene"},{"created":"2025-04-30T14:56:11.327992+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.321","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EDA were set to ","entity_name":"EDA","entity_type":"gene"},{"created":"2025-04-30T14:55:55.002870+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.320","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ECHS1 as ready","entity_name":"ECHS1","entity_type":"gene"},{"created":"2025-04-30T14:55:54.994891+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.320","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: echs1 has been classified as Green List (High Evidence).","entity_name":"ECHS1","entity_type":"gene"},{"created":"2025-04-30T14:55:52.736850+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.320","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ECHS1 were changed from Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3) to Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency MIM# 616277","entity_name":"ECHS1","entity_type":"gene"},{"created":"2025-04-30T14:55:41.796081+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.319","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ECHS1 were set to ","entity_name":"ECHS1","entity_type":"gene"},{"created":"2025-04-30T14:55:26.246015+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.318","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DYSF as ready","entity_name":"DYSF","entity_type":"gene"},{"created":"2025-04-30T14:55:26.239244+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.318","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dysf has been classified as Green List (High Evidence).","entity_name":"DYSF","entity_type":"gene"},{"created":"2025-04-30T14:55:23.820913+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.318","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DYSF were changed from Muscular dystrophy, limb-girdle, type 2B, 253601 (3) to Miyoshi muscular dystrophy 1 MIM#254130; MONDO:0024545; Muscular dystrophy, limb-girdle, autosomal recessive 2 MIM#253601; MONDO:0009676; Myopathy, distal, with anterior tibial onset MIM#606768; MONDO:0011721","entity_name":"DYSF","entity_type":"gene"},{"created":"2025-04-30T14:55:13.911643+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.317","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DYSF were set to ","entity_name":"DYSF","entity_type":"gene"},{"created":"2025-04-30T14:54:47.795489+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.316","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DYNC2H1 as ready","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2025-04-30T14:54:47.787360+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.316","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dync2h1 has been classified as Green List (High Evidence).","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2025-04-30T14:54:42.923750+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.316","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DYNC2H1 were changed from Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 (3) to Short-rib thoracic dysplasia 3 with or without polydactyly, MIM#613091","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2025-04-30T14:54:31.150214+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.315","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DYNC2H1 were set to ","entity_name":"DYNC2H1","entity_type":"gene"},{"created":"2025-04-30T14:54:13.693190+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DYM as ready","entity_name":"DYM","entity_type":"gene"},{"created":"2025-04-30T14:54:13.686396+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dym has been classified as Green List (High Evidence).","entity_name":"DYM","entity_type":"gene"},{"created":"2025-04-30T14:54:11.408594+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DYM were changed from Dyggve-Melchior-Clausen disease, 223800 (3) to Dyggve-Melchior-Clausen disease MIM#223800; Smith-McCort dysplasia MIM#607326","entity_name":"DYM","entity_type":"gene"},{"created":"2025-04-30T14:54:00.994161+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.313","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DYM were set to ","entity_name":"DYM","entity_type":"gene"},{"created":"2025-04-30T14:53:42.968175+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.312","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOK7 as ready","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-04-30T14:53:42.957997+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.312","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dok7 has been classified as Green List (High Evidence).","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-04-30T14:53:40.871894+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.312","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOK7 were changed from Myasthenic syndrome, congenital, 10, 254300 (3) to Myasthenic syndrome, congenital, 10, MIM# 254300; Fetal akinesia deformation sequence 3, MIM# 618389","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-04-30T14:53:31.459766+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.311","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DOK7 were set to ","entity_name":"DOK7","entity_type":"gene"},{"created":"2025-04-30T14:53:13.289348+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.310","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOCK6 as ready","entity_name":"DOCK6","entity_type":"gene"},{"created":"2025-04-30T14:53:13.282660+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.310","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dock6 has been classified as Green List (High Evidence).","entity_name":"DOCK6","entity_type":"gene"},{"created":"2025-04-30T14:53:11.069183+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.310","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOCK6 were changed from Adams-Oliver syndrome 2, 614219 (3) to Adams-Oliver syndrome 2, MIM# 614219","entity_name":"DOCK6","entity_type":"gene"},{"created":"2025-04-30T14:53:00.872453+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.309","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DOCK6 were set to ","entity_name":"DOCK6","entity_type":"gene"},{"created":"2025-04-30T14:52:43.288034+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.308","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNMT3B as ready","entity_name":"DNMT3B","entity_type":"gene"},{"created":"2025-04-30T14:52:43.281571+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.308","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnmt3b has been classified as Green List (High Evidence).","entity_name":"DNMT3B","entity_type":"gene"},{"created":"2025-04-30T14:52:41.198034+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.308","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNMT3B were changed from Immunodeficiency-centromeric instability-facial anomalies syndrome 1, 242860 (3) to Immunodeficiency-centromeric instability-facial anomalies syndrome 1 (MIM#242860)","entity_name":"DNMT3B","entity_type":"gene"},{"created":"2025-04-30T14:52:19.263444+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.307","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI2 as ready","entity_name":"DNAI2","entity_type":"gene"},{"created":"2025-04-30T14:52:19.253857+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.307","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai2 has been classified as Green List (High Evidence).","entity_name":"DNAI2","entity_type":"gene"},{"created":"2025-04-30T14:52:14.491227+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.307","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI2 were changed from Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 (3) to Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444","entity_name":"DNAI2","entity_type":"gene"},{"created":"2025-04-30T14:51:58.901419+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.306","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI2 were set to ","entity_name":"DNAI2","entity_type":"gene"},{"created":"2025-04-30T14:51:34.993463+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.305","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI1 as ready","entity_name":"DNAI1","entity_type":"gene"},{"created":"2025-04-30T14:51:34.986904+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.305","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai1 has been classified as Green List (High Evidence).","entity_name":"DNAI1","entity_type":"gene"},{"created":"2025-04-30T14:51:31.654371+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.305","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI1 were changed from Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3) to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400","entity_name":"DNAI1","entity_type":"gene"},{"created":"2025-04-30T14:51:20.075619+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.304","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI1 were set to ","entity_name":"DNAI1","entity_type":"gene"},{"created":"2025-04-30T14:50:55.277578+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.303","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH5 as ready","entity_name":"DNAH5","entity_type":"gene"},{"created":"2025-04-30T14:50:55.271430+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.303","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah5 has been classified as Green List (High Evidence).","entity_name":"DNAH5","entity_type":"gene"},{"created":"2025-04-30T14:50:52.788287+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.303","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH5 were changed from Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 (3) to Ciliary dyskinesia, primary, 3, with or without situs inversus MIM#608644","entity_name":"DNAH5","entity_type":"gene"},{"created":"2025-04-30T14:50:42.896422+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.302","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH5 were set to ","entity_name":"DNAH5","entity_type":"gene"},{"created":"2025-04-30T14:50:25.907405+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.301","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH11 as ready","entity_name":"DNAH11","entity_type":"gene"},{"created":"2025-04-30T14:50:25.901141+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.301","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah11 has been classified as Green List (High Evidence).","entity_name":"DNAH11","entity_type":"gene"},{"created":"2025-04-30T14:50:23.657366+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.301","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH11 were changed from Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3) to Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884","entity_name":"DNAH11","entity_type":"gene"},{"created":"2025-04-30T14:50:13.267257+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.300","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH11 were set to ","entity_name":"DNAH11","entity_type":"gene"},{"created":"2025-04-30T14:49:49.765783+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.299","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DMD as ready","entity_name":"DMD","entity_type":"gene"},{"created":"2025-04-30T14:49:49.748217+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.299","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmd has been classified as Green List (High Evidence).","entity_name":"DMD","entity_type":"gene"},{"created":"2025-04-30T14:49:47.281259+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.299","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DMD were changed from Duchenne muscular dystrophy, 310200 (3) to Duchenne muscular dystrophy MIM#310200","entity_name":"DMD","entity_type":"gene"},{"created":"2025-04-30T14:49:35.560266+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.298","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DMD were set to ","entity_name":"DMD","entity_type":"gene"},{"created":"2025-04-30T14:49:18.699484+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.297","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLL3 as ready","entity_name":"DLL3","entity_type":"gene"},{"created":"2025-04-30T14:49:18.691633+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.297","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dll3 has been classified as Green List (High Evidence).","entity_name":"DLL3","entity_type":"gene"},{"created":"2025-04-30T14:49:16.327761+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.297","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLL3 were changed from Spondylocostal dysostosis 1, autosomal recessive, 277300 (3) to Spondylocostal dysostosis 1, autosomal recessive, MIM# 277300; MONDO:0020692","entity_name":"DLL3","entity_type":"gene"},{"created":"2025-04-30T14:49:06.938286+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.296","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLL3 were set to ","entity_name":"DLL3","entity_type":"gene"},{"created":"2025-04-30T14:48:46.087705+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.295","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG3 as ready","entity_name":"DLG3","entity_type":"gene"},{"created":"2025-04-30T14:48:46.081636+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.295","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg3 has been classified as Green List (High Evidence).","entity_name":"DLG3","entity_type":"gene"},{"created":"2025-04-30T14:48:43.844670+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.295","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLG3 were changed from Mental retardation, X-linked 90, 300850 (3) to Intellectual developmental disorder, X-linked 90 MIM#300850","entity_name":"DLG3","entity_type":"gene"},{"created":"2025-04-30T14:48:34.888783+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.294","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLG3 were set to ","entity_name":"DLG3","entity_type":"gene"}]}