{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1715","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1713","results":[{"created":"2020-07-23T17:41:06.926955+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3484","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RBM8A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Thrombocytopenia-absent radius syndrome, MIM# 274000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:40:30.605516+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBM8A as ready","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:40:30.592546+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbm8a has been classified as Green List (High Evidence).","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:40:28.562836+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RBM8A were changed from  to Thrombocytopenia-absent radius syndrome, MIM# 274000","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:40:03.504645+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RBM8A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:38:56.553224+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: RBM8A.","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:38:48.379771+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RBM8A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Thrombocytopenia-absent radius syndrome, MIM# 274000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:33:22.969818+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBM8A as ready","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:33:22.958249+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbm8a has been classified as Green List (High Evidence).","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:33:18.061800+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RBM8A as Green List (high evidence)","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:33:18.051269+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbm8a has been classified as Green List (High Evidence).","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:32:51.352043+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RBM8A was added\ngene: RBM8A was added to Radial Ray Abnormalities. Sources: Expert list\nSV/CNV tags were added to gene: RBM8A.\nMode of inheritance for gene: RBM8A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RBM8A were set to Thrombocytopenia-absent radius syndrome, MIM# 274000\nReview for gene: RBM8A was set to GREEN\nAdded comment: Vast majority are due to a recurrent 200kb deletion on one allele (although truncations are seen) and the presence of 1 of 2 SNPs in trans. The SNPs have a MAF of 3.05% and 0.42%. \nSources: Expert list","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:29:16.359294+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RECQL4 as ready","entity_name":"RECQL4","entity_type":"gene"},{"created":"2020-07-23T17:29:16.348963+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: recql4 has been classified as Green List (High Evidence).","entity_name":"RECQL4","entity_type":"gene"},{"created":"2020-07-23T17:29:10.530382+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RECQL4 as Green List (high evidence)","entity_name":"RECQL4","entity_type":"gene"},{"created":"2020-07-23T17:29:10.521968+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: recql4 has been classified as Green List (High Evidence).","entity_name":"RECQL4","entity_type":"gene"},{"created":"2020-07-23T17:28:48.034689+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RECQL4 was added\ngene: RECQL4 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: RECQL4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RECQL4 were set to Baller-Gerold syndrome, MIM#\t218600; RAPADILINO syndrome, MIM#\t266280; Rothmund-Thomson syndrome, type 2,MIM#\t268400\nReview for gene: RECQL4 was set to GREEN\nAdded comment: Well established gene-disease association, radial ray abnormalities are a key feature. \nSources: Expert list","entity_name":"RECQL4","entity_type":"gene"},{"created":"2020-07-23T17:23:24.276802+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3484","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL15 as ready","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:23:24.268653+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl15 has been classified as Green List (High Evidence).","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:23:04.490618+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3484","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL15 were changed from  to Diamond-Blackfan anemia 12, MIM# 615550","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:22:45.271556+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3483","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL15 were set to ","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:22:27.524400+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3482","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL15 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:22:10.077354+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3481","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPL15: Rating: GREEN; Mode of pathogenicity: None; Publications: 23812780, 29599205; Phenotypes: Diamond-Blackfan anemia 12, MIM# 615550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:49.957274+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL15 as ready","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:49.947208+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl15 has been classified as Green List (High Evidence).","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:47.295298+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL15 were changed from Diamond-Blackfan anemia 12, MIM# 615550 to Diamond-Blackfan anemia 12, MIM# 615550","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:34.249971+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL15 were changed from  to Diamond-Blackfan anemia 12, MIM# 615550","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:26.924898+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL15 as ready","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:26.914478+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl15 has been classified as Green List (High Evidence).","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:20:18.120501+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL15 were set to ","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:19:57.294355+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL15 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:19:30.642319+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPL15: Rating: GREEN; Mode of pathogenicity: None; Publications: 23812780, 29599205; Phenotypes: Diamond-Blackfan anemia 12, MIM# 615550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:19:21.298175+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPL15 as Green List (high evidence)","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:19:21.287836+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl15 has been classified as Green List (High Evidence).","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T17:18:52.732738+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPL15 was added\ngene: RPL15 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: RPL15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: RPL15 were set to 23812780; 29599205\nPhenotypes for gene: RPL15 were set to Diamond-Blackfan anemia 12, MIM#\t615550\nReview for gene: RPL15 was set to GREEN\nAdded comment: Seven unrelated individuals reported to date. \nSources: Expert list","entity_name":"RPL15","entity_type":"gene"},{"created":"2020-07-23T16:24:38.204333+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:24:38.194308+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:24:35.376231+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS28 were changed from  to Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:24:10.629349+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS28 were set to ","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:23:50.483226+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS28 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:23:29.638233+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Amber List (moderate evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:23:29.630060+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:23:05.365216+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:22:21.296912+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3481","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:22:21.245160+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3481","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:22:14.477015+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3481","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS28 were changed from  to Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:21:58.620284+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3480","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS28 were set to ","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:21:43.282201+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3479","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS28 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:21:27.715269+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3478","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Amber List (moderate evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:21:27.703589+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3478","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:21:12.520939+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3477","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:20:26.640420+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:20:26.631224+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:20:23.298322+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS28 were changed from  to Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:19:56.026016+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS28 were set to ","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:19:36.065812+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS28 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:18:50.201947+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Amber List (moderate evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:18:50.191248+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T16:18:24.596413+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:29:42.314265+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:29:42.302787+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:29:39.464842+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS28 were changed from  to Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:29:23.344247+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS28 were set to ","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:28:57.452493+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS28 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:28:37.505085+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Amber List (moderate evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:28:37.496818+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:28:15.620530+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:27:09.359690+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS28 as ready","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:27:09.350559+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Red List (Low Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:27:06.521706+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS28 were changed from  to Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:26:40.558616+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS28 were set to ","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:26:21.962037+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS28 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:25:48.747098+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS28 as Red List (low evidence)","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:25:48.735585+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps28 has been classified as Red List (Low Evidence).","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:25:21.295943+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS28: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS28","entity_type":"gene"},{"created":"2020-07-23T11:22:51.183087+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3477","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS29 as ready","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:22:51.172365+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3477","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:22:43.754659+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3477","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS29 were changed from  to Diamond-Blackfan anemia 13, MIM# 615909","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:22:24.641717+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3476","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS29 were set to ","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:22:04.779398+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3475","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS29 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:21:45.814615+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3474","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS29 as Amber List (moderate evidence)","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:21:45.805310+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3474","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:21:26.887111+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3473","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS29: Rating: AMBER; Mode of pathogenicity: None; Publications: 24829207; Phenotypes: Diamond-Blackfan anemia 13, MIM# 615909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:20:34.009138+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS29 as ready","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:20:33.997855+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:20:31.503056+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS29 were changed from  to Diamond-Blackfan anemia 13, MIM# 615909","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:20:04.057788+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS29 were set to ","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:19:41.219952+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS29 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:19:15.641025+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS29 as Amber List (moderate evidence)","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:19:15.630635+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:18:48.405055+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS29: Rating: AMBER; Mode of pathogenicity: None; Publications: 24829207; Phenotypes: Diamond-Blackfan anemia 13, MIM# 615909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:18:14.028040+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS29 as ready","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:18:14.016182+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:18:10.978152+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS29 were changed from  to Diamond-Blackfan anemia 13, MIM# 615909","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:17:44.914548+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS29 were set to ","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:17:23.282558+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS29 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:16:59.213988+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPS29 as Amber List (moderate evidence)","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:16:59.203702+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps29 has been classified as Amber List (Moderate Evidence).","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:16:33.628042+10:00","panel_name":"Diamond Blackfan anaemia","panel_id":98,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPS29: Rating: AMBER; Mode of pathogenicity: None; Publications: 24829207; Phenotypes: Diamond-Blackfan anemia 13, MIM# 615909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS29","entity_type":"gene"},{"created":"2020-07-23T11:16:19.940450+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"RPS29","entity_type":"gene"}]}