{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1714","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1712","results":[{"created":"2020-07-24T09:47:39.554509+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Tag refuted tag was added to gene: FANCM.","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:47:25.298216+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCM as ready","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:47:25.286853+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:47:23.278105+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCM were changed from  to Fanconi anaemia","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:46:58.305458+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCM were set to ","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:46:18.747925+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:45:58.674181+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCM as Red List (low evidence)","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:45:58.665982+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:45:36.248119+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FANCM: Rating: RED; Mode of pathogenicity: None; Publications: 28837162; Phenotypes: Fanconi anaemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:44:35.720641+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCM as ready","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:44:35.704819+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:44:32.841692+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCM were changed from  to Fanconi anaemia","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:43:58.710780+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCM were set to ","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:43:30.793542+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:43:11.202134+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCM as Red List (low evidence)","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:43:11.192259+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:42:48.345558+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FANCM: Rating: RED; Mode of pathogenicity: None; Publications: 28837162; Phenotypes: Fanconi anaemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCM","entity_type":"gene"},{"created":"2020-07-24T09:39:10.153724+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGFR2 was added\ngene: FGFR2 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: FGFR2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FGFR2 were set to LADD syndrome, MIM#149730\nReview for gene: FGFR2 was set to GREEN\nAdded comment: Well established gene-disease association. Radial ray abnormalities are a feature of LADD syndrome. \nSources: Expert list","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-07-24T09:36:13.426047+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR3 as ready","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-24T09:36:13.417204+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-24T09:36:08.899965+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGFR3 as Green List (high evidence)","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-24T09:36:08.890143+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-24T09:35:35.783412+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGFR3 was added\ngene: FGFR3 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: FGFR3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FGFR3 were set to LADD syndrome, MIM#149730\nReview for gene: FGFR3 was set to GREEN\nAdded comment: Well established gene-disease association. Variable radial ray defects (at the most severe, bilateral radial aplasia) are a feature of LADD syndrome. \nSources: Expert list","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-24T09:32:08.029034+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FIG4 as ready","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-07-24T09:32:08.019990+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Green List (High Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-07-24T09:32:03.525584+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FIG4 as Green List (high evidence)","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-07-24T09:32:03.515751+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Green List (High Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-07-24T09:31:36.871551+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FIG4 was added\ngene: FIG4 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: FIG4 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FIG4 were set to 23623387\nPhenotypes for gene: FIG4 were set to Yunis-Varon syndrome, MIM#\t216340\nReview for gene: FIG4 was set to GREEN\nAdded comment: Absent thumbs are a feature of Yunis-Varon syndrome. \nSources: Expert list","entity_name":"FIG4","entity_type":"gene"},{"created":"2020-07-24T09:28:46.877172+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLNA as ready","entity_name":"FLNA","entity_type":"gene"},{"created":"2020-07-24T09:28:46.868098+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flna has been classified as Green List (High Evidence).","entity_name":"FLNA","entity_type":"gene"},{"created":"2020-07-24T09:28:42.912229+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FLNA as Green List (high evidence)","entity_name":"FLNA","entity_type":"gene"},{"created":"2020-07-24T09:28:42.901051+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flna has been classified as Green List (High Evidence).","entity_name":"FLNA","entity_type":"gene"},{"created":"2020-07-24T09:28:16.803357+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FLNA was added\ngene: FLNA was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: FLNA was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPublications for gene: FLNA were set to 12612583\nPhenotypes for gene: FLNA were set to Melnick-Needles syndrome, 309350\nReview for gene: FLNA was set to GREEN\nAdded comment: Melnick-Needles associated with radial shortening in affected women. Male fetuses reported with absent thumbs \nSources: Expert list","entity_name":"FLNA","entity_type":"gene"},{"created":"2020-07-24T09:25:23.880803+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA1 as ready","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-07-24T09:25:23.871645+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Red List (Low Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-07-24T09:25:00.358343+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA1 as Red List (low evidence)","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-07-24T09:25:00.346777+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Red List (Low Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-07-24T09:24:33.173037+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GATA1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-07-24T09:19:58.572696+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HDAC8 as ready","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:19:58.560981+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Red List (Low Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:19:56.387406+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HDAC8 were changed from  to Cornelia de Lange syndrome 5, MIM# 300882","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:19:35.845697+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HDAC8 were set to ","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:19:15.756007+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HDAC8 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:18:56.287407+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HDAC8 as Red List (low evidence)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:18:56.277035+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Red List (Low Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:18:28.577269+10:00","panel_name":"Congenital diaphragmatic hernia","panel_id":69,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HDAC8: Rating: RED; Mode of pathogenicity: None; Publications: 30614194, 24403048; Phenotypes: Cornelia de Lange syndrome 5, MIM# 300882; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:14:44.396702+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HDAC8 as ready","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:14:44.388360+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Green List (High Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:12:31.774056+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HDAC8 were changed from  to Cornelia de Lange syndrome 5, MIM# 300882","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:12:05.760608+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HDAC8 were set to ","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:09:09.382260+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HDAC8 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:08:41.162654+10:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HDAC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 30614194, 24403048; Phenotypes: Cornelia de Lange syndrome 5, MIM# 300882; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:00:43.103364+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3489","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HDAC8 as ready","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:00:43.094809+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3489","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Green List (High Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:00:36.756206+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3489","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HDAC8 were changed from  to Cornelia de Lange syndrome 5, MIM# 300882","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:00:20.625560+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3488","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HDAC8 were set to ","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T09:00:02.149130+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3487","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HDAC8 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:59:41.359302+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HDAC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 30614194, 24403048; Phenotypes: Cornelia de Lange syndrome 5, MIM# 300882; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:57:05.632230+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HDAC8 as ready","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:57:05.623213+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Green List (High Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:56:48.762555+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HDAC8 were changed from  to Cornelia de Lange syndrome 5, MIM# 300882","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:56:18.323476+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2782","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HDAC8 were set to ","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:55:54.725038+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2781","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HDAC8 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:55:29.641889+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2780","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HDAC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 30614194, 24403048; Phenotypes: Cornelia de Lange syndrome 5, MIM# 300882; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:54:24.116739+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HDAC8 as ready","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:54:24.108055+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Green List (High Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:54:19.254290+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HDAC8 as Green List (high evidence)","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:54:19.246230+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hdac8 has been classified as Green List (High Evidence).","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-24T08:52:15.059403+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HDAC8 was added\ngene: HDAC8 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: HDAC8 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPublications for gene: HDAC8 were set to 30614194; 24403048\nPhenotypes for gene: HDAC8 were set to Cornelia de Lange syndrome 5, MIM#\t300882\nReview for gene: HDAC8 was set to GREEN\nAdded comment: Well established CdL gene. \nSources: Expert list","entity_name":"HDAC8","entity_type":"gene"},{"created":"2020-07-23T18:17:45.711121+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HOXA13 as ready","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-23T18:17:45.691360+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa13 has been classified as Green List (High Evidence).","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-23T18:17:40.934347+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HOXA13 as Green List (high evidence)","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-23T18:17:40.926391+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa13 has been classified as Green List (High Evidence).","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-23T18:17:18.278514+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HOXA13 was added\ngene: HOXA13 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: HOXA13 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: HOXA13 were set to Hand-foot-uterus syndrome, MIM# 140000\nReview for gene: HOXA13 was set to GREEN\nAdded comment: Well established gene-disease association, hypoplastic thumbs reported. \nSources: Expert list","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-23T18:12:05.096418+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMBR1 as ready","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-23T18:12:05.087280+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmbr1 has been classified as Green List (High Evidence).","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-23T18:12:00.041258+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LMBR1 as Green List (high evidence)","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-23T18:12:00.005867+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmbr1 has been classified as Green List (High Evidence).","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-23T18:11:33.688327+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LMBR1 was added\ngene: LMBR1 was added to Radial Ray Abnormalities. Sources: Expert list\nSV/CNV tags were added to gene: LMBR1.\nMode of inheritance for gene: LMBR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: LMBR1 were set to Laurin-Sandrow syndrome, MIM#\t135750\nReview for gene: LMBR1 was set to GREEN\nAdded comment: Radial aplasia but with ulnar dimelia. Reported microduplications in LMBR1 associated with Laurin-Sandrow syndrome are in the SHH regulatory element (ZRS) that resides in intron 5 of the LMBR1 gene. Duplications are >10kb. \nSources: Expert list","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-23T18:06:19.630898+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIPBL as ready","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-07-23T18:06:19.612910+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nipbl has been classified as Green List (High Evidence).","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-07-23T18:06:15.450360+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIPBL as Green List (high evidence)","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-07-23T18:06:15.442217+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nipbl has been classified as Green List (High Evidence).","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-07-23T18:05:53.842668+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NIPBL was added\ngene: NIPBL was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: NIPBL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NIPBL were set to Cornelia de Lange syndrome 1, MIM#\t122470\nReview for gene: NIPBL was set to GREEN\nAdded comment: Well established gene-disease association. Radial ray abnormalities are a key part of the phenotype. \nSources: Expert list","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-07-23T17:56:33.511372+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAD21 as ready","entity_name":"RAD21","entity_type":"gene"},{"created":"2020-07-23T17:56:33.499010+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad21 has been classified as Green List (High Evidence).","entity_name":"RAD21","entity_type":"gene"},{"created":"2020-07-23T17:56:26.583553+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAD21 as Green List (high evidence)","entity_name":"RAD21","entity_type":"gene"},{"created":"2020-07-23T17:56:26.573528+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad21 has been classified as Green List (High Evidence).","entity_name":"RAD21","entity_type":"gene"},{"created":"2020-07-23T17:56:01.382885+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RAD21 was added\ngene: RAD21 was added to Radial Ray Abnormalities. Sources: Expert list\nMode of inheritance for gene: RAD21 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: RAD21 were set to 32193685\nPhenotypes for gene: RAD21 were set to Cornelia de Lange syndrome 4, MIM# 614701\nReview for gene: RAD21 was set to GREEN\nAdded comment: Recent large series of over 40 affected individuals published. Radial ray abnormalities are part of the phenotype. \nSources: Expert list","entity_name":"RAD21","entity_type":"gene"},{"created":"2020-07-23T17:51:42.288590+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAD51C as ready","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:51:42.280262+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad51c has been classified as Green List (High Evidence).","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:51:40.071367+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAD51C were changed from  to Fanconi anemia, complementation group O, MIM# 613390","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:51:19.802892+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAD51C were set to ","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:50:53.728209+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAD51C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:50:29.682825+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAD51C: Rating: GREEN; Mode of pathogenicity: None; Publications: 29278735, 20400963; Phenotypes: Fanconi anemia, complementation group O, MIM# 613390; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAD51C","entity_type":"gene"},{"created":"2020-07-23T17:42:28.587296+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3486","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: RBM8A.","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:41:47.541236+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBM8A as ready","entity_name":"RBM8A","entity_type":"gene"},{"created":"2020-07-23T17:41:47.532282+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3486","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":"2020-07-23T17:41:40.377159+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3486","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":"2020-07-23T17:41:23.082307+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3485","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"}]}