{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1342","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1340","results":[{"created":"2021-04-24T11:29:40.733695+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancc has been classified as Green List (High Evidence).","entity_name":"FANCC","entity_type":"gene"},{"created":"2021-04-24T11:29:30.795958+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCC were changed from  to Fanconi anaemia, complementation group C, MIM# 227645; MONDO:0009213","entity_name":"FANCC","entity_type":"gene"},{"created":"2021-04-24T11:28:59.901376+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCC were set to ","entity_name":"FANCC","entity_type":"gene"},{"created":"2021-04-24T11:28:37.909040+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCC","entity_type":"gene"},{"created":"2021-04-24T11:27:54.609507+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC4 as ready","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:27:54.598950+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc4 has been classified as Green List (High Evidence).","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:27:52.249137+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC4 were changed from  to Fanconi aanemia, complementation group Q, MIM# 615272; MONDO:0014108","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:27:29.981270+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC4 were set to ","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:27:01.499172+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:26:30.061326+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ERCC4: Changed phenotypes: Fanconi aanemia, complementation group Q, MIM# 615272, MONDO:0014108","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:26:12.372107+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:26:06.456507+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ERCC4: Added comment: Bi-allelic variants in this gene are associated with a range of phenotypes, including FA and radial ray defects.; Changed phenotypes: Fanconi anemia, complementation group Q, MIM# 615272, MONDO:0014108","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:22:49.739260+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRIP1 as ready","entity_name":"BRIP1","entity_type":"gene"},{"created":"2021-04-24T11:22:49.726582+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brip1 has been classified as Green List (High Evidence).","entity_name":"BRIP1","entity_type":"gene"},{"created":"2021-04-24T11:22:46.374774+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRIP1 were changed from  to Fanconi anaemia, complementation group J, MIM# 609054","entity_name":"BRIP1","entity_type":"gene"},{"created":"2021-04-24T11:22:14.542450+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRIP1","entity_type":"gene"},{"created":"2021-04-24T11:21:39.639642+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRCA2 as ready","entity_name":"BRCA2","entity_type":"gene"},{"created":"2021-04-24T11:21:39.628488+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brca2 has been classified as Green List (High Evidence).","entity_name":"BRCA2","entity_type":"gene"},{"created":"2021-04-24T11:21:36.449655+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRCA2 were changed from  to Fanconi anaemia, complementation group D1, MIM# 605724","entity_name":"BRCA2","entity_type":"gene"},{"created":"2021-04-24T11:20:54.639842+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRCA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRCA2","entity_type":"gene"},{"created":"2021-04-24T11:20:24.300345+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BRCA2: Changed phenotypes: Fanconi anaemia, complementation group D1, MIM# 605724","entity_name":"BRCA2","entity_type":"gene"},{"created":"2021-04-24T11:18:47.946388+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-04-24T11:17:14.932480+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPC as ready","entity_name":"XPC","entity_type":"gene"},{"created":"2021-04-24T11:17:14.912667+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpc has been classified as Green List (High Evidence).","entity_name":"XPC","entity_type":"gene"},{"created":"2021-04-24T11:17:12.072760+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPC were changed from  to Xeroderma pigmentosum, group C, MIM# 278720; MONDO:0010211","entity_name":"XPC","entity_type":"gene"},{"created":"2021-04-24T11:16:43.215073+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPC were set to ","entity_name":"XPC","entity_type":"gene"},{"created":"2021-04-24T11:16:20.014528+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPC","entity_type":"gene"},{"created":"2021-04-24T11:15:48.136967+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPA as ready","entity_name":"XPA","entity_type":"gene"},{"created":"2021-04-24T11:15:48.126851+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpa has been classified as Green List (High Evidence).","entity_name":"XPA","entity_type":"gene"},{"created":"2021-04-24T11:15:39.559045+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPA were changed from  to Xeroderma pigmentosum, group A , MIM#278700; MONDO:0010210","entity_name":"XPA","entity_type":"gene"},{"created":"2021-04-24T11:15:12.446017+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPA were set to ","entity_name":"XPA","entity_type":"gene"},{"created":"2021-04-24T11:14:44.017486+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: XPA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"XPA","entity_type":"gene"},{"created":"2021-04-24T11:13:46.793373+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TYR as ready","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:13:46.782423+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyr has been classified as Red List (Low Evidence).","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:13:43.698630+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TYR were changed from  to Albinism, oculocutaneous, type IA, MIM# 203100","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:13:18.827557+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TYR as Red List (low evidence)","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:13:18.817858+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyr has been classified as Red List (Low Evidence).","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:12:54.227465+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TYR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Albinism, oculocutaneous, type IA, MIM# 203100; Mode of inheritance: None","entity_name":"TYR","entity_type":"gene"},{"created":"2021-04-24T11:12:04.205423+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RECQL4 were set to 12838562; 10319867; 20503338; 18716613; 18616953","entity_name":"RECQL4","entity_type":"gene"},{"created":"2021-04-24T11:10:58.679536+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC8 as ready","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T11:10:58.668883+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc8 has been classified as Green List (High Evidence).","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T11:10:47.859320+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC8 were changed from  to Cockayne syndrome, type A, MIM# 216400; MONDO:0019569; UV-sensitive syndrome 2, MIM# 614621; MONDO:0013829","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T11:10:19.911716+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC8 were set to ","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T11:09:56.842064+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T11:09:21.138247+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC6 as ready","entity_name":"ERCC6","entity_type":"gene"},{"created":"2021-04-24T11:09:21.095760+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc6 has been classified as Green List (High Evidence).","entity_name":"ERCC6","entity_type":"gene"},{"created":"2021-04-24T11:09:17.797027+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC6 were changed from  to Cerebrooculofacioskeletal syndrome 1, MIM# 214150; MONDO:0008955; Cockayne syndrome, type B, MIM# 133540; MONDO:0019570; De Sanctis-Cacchione syndrome, MIM# 278800; MONDO:0010217; UV-sensitive syndrome 1, MIM# 600630; MONDO:0010909","entity_name":"ERCC6","entity_type":"gene"},{"created":"2021-04-24T11:08:48.024889+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC6","entity_type":"gene"},{"created":"2021-04-24T11:08:19.534391+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC5 as ready","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:08:19.519398+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc5 has been classified as Green List (High Evidence).","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:08:16.175908+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC5 were changed from  to Cerebrooculofacioskeletal syndrome 3, MIM# 616570; MONDO:0014696; Xeroderma pigmentosum, group G, MIM# 278780; MONDO:0010216","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:07:41.455253+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC5 were set to ","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:07:18.698748+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:06:48.839339+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association, spectrum of severity, including antenatal presentation with arthrogryposis.; to: Well established gene-disease association, spectrum of severity, photosensitivity is a feature.","entity_name":"ERCC5","entity_type":"gene"},{"created":"2021-04-24T11:06:26.052776+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC4 as ready","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:06:26.039939+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc4 has been classified as Green List (High Evidence).","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:06:22.682865+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC4 were changed from  to Fanconi anaemia, complementation group Q, MIM# 615272; MONDO:0014108; Xeroderma pigmentosum, group F, MIM# 278760; MONDO:0010215; XFE progeroid syndrome, MIM# 610965; MONDO:0012590","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:05:35.708157+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC4 were set to ","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:05:07.517579+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC4","entity_type":"gene"},{"created":"2021-04-24T11:04:28.655744+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC3 as ready","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T11:04:28.645306+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc3 has been classified as Green List (High Evidence).","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T11:04:25.703240+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC3 were changed from  to Trichothiodystrophy 2, photosensitive, MIM# 616390; Xeroderma pigmentosum, group B 61, MIM#0651","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T11:03:53.296468+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC3 were set to ","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T11:03:23.584776+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T11:02:58.743793+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Nucleotide excision repair disorder, variable severity.; to: Nucleotide excision repair disorder, variable severity, photosensitivity is a feature.","entity_name":"ERCC3","entity_type":"gene"},{"created":"2021-04-24T08:37:56.014522+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC1 as ready","entity_name":"ERCC1","entity_type":"gene"},{"created":"2021-04-24T08:37:56.004898+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc1 has been classified as Green List (High Evidence).","entity_name":"ERCC1","entity_type":"gene"},{"created":"2021-04-24T08:37:53.653134+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC1 were changed from  to Cerebrooculofacioskeletal syndrome 4, MIM# 610758","entity_name":"ERCC1","entity_type":"gene"},{"created":"2021-04-24T08:37:31.680443+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC1 were set to ","entity_name":"ERCC1","entity_type":"gene"},{"created":"2021-04-24T08:37:08.766617+10:00","panel_name":"Photosensitivity Syndromes","panel_id":156,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC1","entity_type":"gene"},{"created":"2021-04-24T08:35:15.402141+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-04-24T08:35:04.226073+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TYR from the panel","entity_name":null,"entity_type":null},{"created":"2021-04-24T08:33:57.369533+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC8 as ready","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T08:33:57.358201+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc8 has been classified as Green List (High Evidence).","entity_name":"ERCC8","entity_type":"gene"},{"created":"2021-04-24T08:31:22.045058+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNKP as ready","entity_name":"PNKP","entity_type":"gene"},{"created":"2021-04-24T08:31:22.029798+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnkp has been classified as Green List (High Evidence).","entity_name":"PNKP","entity_type":"gene"},{"created":"2021-04-24T08:31:12.360999+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PNKP as Green List (high evidence)","entity_name":"PNKP","entity_type":"gene"},{"created":"2021-04-24T08:31:12.351874+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnkp has been classified as Green List (High Evidence).","entity_name":"PNKP","entity_type":"gene"},{"created":"2021-04-24T08:30:48.677954+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PNKP was added\ngene: PNKP was added to Chromosome Breakage Disorders. Sources: Expert Review\nMode of inheritance for gene: PNKP was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PNKP were set to 20118933; 25728773\nPhenotypes for gene: PNKP were set to Ataxia-oculomotor apraxia 4, MIM#\t616267; Microcephaly, seizures, and developmental delay, MIM#\t613402\nReview for gene: PNKP was set to GREEN\nAdded comment: Enzyme involved in DNA repair.\r\n\r\nAtaxia-oculomotor apraxia 4, MIM#\t616267 typically has onset in first decade, whereas Microcephaly, seizures, and developmental delay, MIM#\t613402 is congenital. \nSources: Expert Review","entity_name":"PNKP","entity_type":"gene"},{"created":"2021-04-24T08:25:08.824283+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7317","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HELLS as ready","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:25:08.814400+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7317","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hells has been classified as Green List (High Evidence).","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:25:01.054023+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7317","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HELLS were changed from  to Immunodeficiency-centromeric instability-facial anomalies syndrome 4, MIM# 616911; MONDO:0014829","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:24:43.473265+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7316","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HELLS were set to ","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:24:26.784212+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7315","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HELLS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:24:08.879191+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7314","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HELLS: Rating: GREEN; Mode of pathogenicity: None; Publications: 26216346; Phenotypes: Immunodeficiency-centromeric instability-facial anomalies syndrome 4, MIM# 616911, MONDO:0014829; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:23:23.178786+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HELLS as ready","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:23:23.168154+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hells has been classified as Green List (High Evidence).","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:23:18.530242+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HELLS as Green List (high evidence)","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:23:18.520672+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hells has been classified as Green List (High Evidence).","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:22:49.393179+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HELLS was added\ngene: HELLS was added to Chromosome Breakage Disorders. Sources: Expert Review\nMode of inheritance for gene: HELLS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HELLS were set to 26216346\nPhenotypes for gene: HELLS were set to Immunodeficiency-centromeric instability-facial anomalies syndrome 4, MIM#\t616911; MONDO:0014829\nReview for gene: HELLS was set to GREEN\nAdded comment: Immunodeficiency-centromeric instability-facial anomalies syndrome-4 is characterized by recurrent infections in childhood and variable dysmorphic facial features. Laboratory studies show hypomethylation of certain chromosomal regions. Additional features, including delayed development, are variable.\r\n\r\nAt least 4 unrelated families reported. \nSources: Expert Review","entity_name":"HELLS","entity_type":"gene"},{"created":"2021-04-24T08:20:28.380781+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7314","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZBTB24 as ready","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:20:28.368658+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7314","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb24 has been classified as Green List (High Evidence).","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:20:14.119093+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7314","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZBTB24 were changed from  to Immunodeficiency-centromeric instability-facial anomalies syndrome 2, MIM# 614069; MONDO:0013553","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:19:51.894081+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7313","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZBTB24 were set to ","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:19:29.565887+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7312","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZBTB24 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:19:02.762566+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7311","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZBTB24: Rating: GREEN; Mode of pathogenicity: None; Publications: 21596365, 21906047, 23486536; Phenotypes: Immunodeficiency-centromeric instability-facial anomalies syndrome 2, MIM# 614069, MONDO:0013553; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:18:05.300199+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZBTB24 as ready","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:18:05.286885+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb24 has been classified as Green List (High Evidence).","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:17:31.973846+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZBTB24 as Green List (high evidence)","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2021-04-24T08:17:31.964333+10:00","panel_name":"Chromosome Breakage Disorders","panel_id":79,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb24 has been classified as Green List (High Evidence).","entity_name":"ZBTB24","entity_type":"gene"}]}