{"count":220437,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1292","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1290","results":[{"created":"2021-06-19T12:11:41.542872+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: popdc3 has been classified as Green List (High Evidence).","entity_name":"POPDC3","entity_type":"gene"},{"created":"2021-06-19T12:11:25.006807+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POPDC3 as Green List (high evidence)","entity_name":"POPDC3","entity_type":"gene"},{"created":"2021-06-19T12:11:24.996446+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: popdc3 has been classified as Green List (High Evidence).","entity_name":"POPDC3","entity_type":"gene"},{"created":"2021-06-19T12:11:12.751717+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"gene: POPDC3 was added\ngene: POPDC3 was added to Limb Girdle Muscular Dystrophy. Sources: Literature\nMode of inheritance for gene: POPDC3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POPDC3 were set to 31610034\nPhenotypes for gene: POPDC3 were set to Muscular dystrophy, limb-girdle, autosomal recessive 26, MIM#\t618848\nReview for gene: POPDC3 was set to GREEN\nAdded comment: 5 affected individuals from 3 unrelated families reported, supportive animal model data. \nSources: Literature","entity_name":"POPDC3","entity_type":"gene"},{"created":"2021-06-19T12:08:58.410445+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8077","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACD as ready","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:08:58.400948+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8077","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acd has been classified as Red List (Low Evidence).","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:08:50.319004+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8077","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACD were changed from  to Dyskeratosis congenita, MIM# 616553","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:08:29.186031+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8076","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACD were set to ","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:08:12.059157+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8075","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACD was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:07:52.195166+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8074","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACD as Red List (low evidence)","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:07:52.185706+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8074","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acd has been classified as Red List (Low Evidence).","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:06:52.667410+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8073","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACD: Rating: RED; Mode of pathogenicity: None; Publications: 25205116, 25233904; Phenotypes: Dyskeratosis congenita, MIM# 616553; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:06:29.608273+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACD as ready","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:06:29.598540+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acd has been classified as Red List (Low Evidence).","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:06:18.354843+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.313","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACD were changed from  to Dyskeratosis congenita, MIM# 616553","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:05:59.050698+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.312","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACD were set to ","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:05:28.655831+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.311","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACD was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:03:36.402670+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACD as Red List (low evidence)","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:03:36.391350+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.310","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acd has been classified as Red List (Low Evidence).","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T12:03:12.569079+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ACD: Rating: RED; Mode of pathogenicity: None; Publications: 25205116, 25233904; Phenotypes: Dyskeratosis congenita, MIM# 616553; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ACD","entity_type":"gene"},{"created":"2021-06-19T11:52:20.408324+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USB1 were changed from Poikiloderma with neutropenia (OMIM #604173) to Poikiloderma with neutropaenia, MIM# 604173; MONDO:0011405","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:52:01.094842+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USB1 were set to 25044170; 27612988","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:51:26.518431+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20004881, 20503306, 34004352, 33624217, 33111394, 32936385, 32620997, 31522452; Phenotypes: Poikiloderma with neutropaenia, MIM# 604173, MONDO:0011405; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:50:48.465161+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8073","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USB1 were changed from Poikiloderma with neutropenia (OMIM #604173) to Poikiloderma with neutropaenia, MIM# 604173; MONDO:0011405","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:50:19.808204+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8072","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USB1 were set to 25044170; 27612988","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:49:54.217867+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8071","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20004881, 20503306, 34004352, 33624217, 33111394, 32936385, 32620997, 31522452; Phenotypes: Poikiloderma with neutropaenia, MIM# 604173, MONDO:0011405; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:49:23.906039+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USB1 as ready","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:49:23.895754+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: usb1 has been classified as Green List (High Evidence).","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:48:50.452321+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.309","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USB1 were changed from  to Poikiloderma with neutropaenia, MIM# 604173; MONDO:0011405","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:48:23.064528+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.308","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USB1 were set to ","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:47:59.734366+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.307","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: USB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:47:31.332381+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20004881, 20503306, 34004352, 33624217, 33111394, 32936385, 32620997, 31522452; Phenotypes: Poikiloderma with neutropaenia, MIM# 604173, MONDO:0011405; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"USB1","entity_type":"gene"},{"created":"2021-06-19T11:43:08.246140+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WAS as ready","entity_name":"WAS","entity_type":"gene"},{"created":"2021-06-19T11:43:08.236372+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: was has been classified as Green List (High Evidence).","entity_name":"WAS","entity_type":"gene"},{"created":"2021-06-19T11:43:05.486115+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.306","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WAS were changed from  to Wiskott-Aldrich syndrome, MIM# 301000; Thrombocytopenia, X-linked, MIM# 313900","entity_name":"WAS","entity_type":"gene"},{"created":"2021-06-19T11:42:19.317375+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WAS was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"WAS","entity_type":"gene"},{"created":"2021-06-18T19:57:40.554787+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.239","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WRAP53 as ready","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:57:40.529815+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.239","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:57:31.100058+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.239","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WRAP53 were changed from Dyskeratosis congenita to Dyskeratosis congenita, autosomal recessive 3, MIM# 613988","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:57:19.036438+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WRAP53 were set to ","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:56:47.461190+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WRAP53 as Green List (high evidence)","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:56:47.448769+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:56:33.915389+10:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.236","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: None; Publications: 21205863, 32303682, 29514627; Phenotypes: Dyskeratosis congenita, autosomal recessive 3, MIM# 613988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:59.873356+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8071","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WRAP53 as ready","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:59.860557+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8071","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:51.679588+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8071","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WRAP53 were changed from  to Dyskeratosis congenita, autosomal recessive 3, MIM# 613988","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:31.341956+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8070","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WRAP53 were set to ","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:15.976894+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8069","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WRAP53 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:55:12.985011+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8069","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WRAP53 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:54:52.379804+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8068","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: None; Publications: 21205863, 32303682, 29514627; Phenotypes: Dyskeratosis congenita, autosomal recessive 3, MIM# 613988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:53:15.634733+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WRAP53 as ready","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:53:15.624561+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:53:12.493748+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WRAP53 were changed from  to Dyskeratosis congenita, autosomal recessive 3, MIM# 613988","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:52:47.966362+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.303","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WRAP53 were set to ","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:52:19.870415+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.302","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WRAP53 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:51:46.236384+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: None; Publications: 21205863, 32303682, 29514627; Phenotypes: Dyskeratosis congenita, autosomal recessive 3, MIM# 613988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-06-18T19:31:07.158739+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAZ as ready","entity_name":"TAZ","entity_type":"gene"},{"created":"2021-06-18T19:31:07.146532+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taz has been classified as Green List (High Evidence).","entity_name":"TAZ","entity_type":"gene"},{"created":"2021-06-18T19:30:31.562900+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.301","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAZ were changed from  to Barth syndrome, MIM# 302060","entity_name":"TAZ","entity_type":"gene"},{"created":"2021-06-18T19:30:04.753240+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAZ was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TAZ","entity_type":"gene"},{"created":"2021-06-18T19:29:38.353737+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Barth syndrome, MIM# 302060; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TAZ","entity_type":"gene"},{"created":"2021-06-18T19:23:03.332038+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SBDS as ready","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-06-18T19:23:03.322167+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sbds has been classified as Green List (High Evidence).","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-06-18T19:22:58.562507+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SBDS were changed from  to Shwachman-Diamond syndrome, MIM# 260400","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-06-18T19:22:27.583107+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SBDS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-06-18T19:21:52.642854+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Shwachman-Diamond syndrome, MIM# 260400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-06-18T18:41:29.078372+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RTEL1 as ready","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:41:29.067037+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rtel1 has been classified as Green List (High Evidence).","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:40:11.483593+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.297","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RTEL1 were changed from  to Dyskeratosis congenita, MIM# 615190; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3, MIM# 616373","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:39:43.191838+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.296","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RTEL1 were set to ","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:39:19.833359+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.295","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RTEL1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:38:48.076290+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RTEL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23453664, 23329068, 25848748, 25607374, 15210109; Phenotypes: Dyskeratosis congenita, MIM# 615190, Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3, MIM# 616373; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RTEL1","entity_type":"gene"},{"created":"2021-06-18T18:27:19.042634+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS10 as ready","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-06-18T18:27:19.032003+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps10 has been classified as Green List (High Evidence).","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-06-18T18:27:12.391382+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.294","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS10 were changed from  to Diamond-Blackfan anaemia 9, MIM# 613308","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-06-18T18:26:41.372035+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.293","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS10 were set to ","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-06-18T18:26:11.377796+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.292","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-06-18T18:24:57.647181+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL5 as ready","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-06-18T18:24:57.635868+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl5 has been classified as Green List (High Evidence).","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-06-18T18:24:54.436317+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.291","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL5 were changed from  to Diamond-Blackfan anaemia 6, MIM# 612561; MONDO:0012937","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-06-18T18:24:27.483477+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.290","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL5 were set to ","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-06-18T18:24:04.738942+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.289","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-06-18T18:21:20.633165+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.287","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2021-06-18T18:21:20.622030+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.287","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2021-06-18T18:21:17.870612+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.287","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMRP were changed from  to Cartilage-hair hypoplasia, MIM# 250250","entity_name":"RMRP","entity_type":"gene"},{"created":"2021-06-18T18:20:53.837496+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.286","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RMRP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RMRP","entity_type":"gene"},{"created":"2021-06-18T18:20:26.849830+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.285","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RMRP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cartilage-hair hypoplasia, MIM# 250250; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RMRP","entity_type":"gene"},{"created":"2021-06-18T18:15:09.519839+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8068","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EP300 as ready","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T18:15:09.505775+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8068","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ep300 has been classified as Green List (High Evidence).","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T18:15:00.203544+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8068","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EP300 were changed from  to Rubinstein-Taybi syndrome 2 MIM#613684; Menke-Hennekam syndrome 2 MIM#618333","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T18:14:46.088355+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8067","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EP300 were set to ","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T18:14:24.208671+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8066","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EP300 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T14:48:41.740578+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8065","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: EP300: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 29460469, 24381114; Phenotypes: Rubinstein-Taybi syndrome 2 MIM#613684, Menke-Hennekam syndrome 2 MIM#618333, Colorectal cancer, somatic MIM#114500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"EP300","entity_type":"gene"},{"created":"2021-06-18T09:28:16.970940+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8065","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PARN as ready","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:28:16.959861+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8065","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: parn has been classified as Green List (High Evidence).","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:28:09.555586+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8065","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PARN were changed from  to Dyskeratosis congenita, autosomal recessive 6, MIM# 616353; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, MIM# 616371","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:27:56.321516+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8064","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PARN were set to ","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:27:32.904822+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8063","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PARN was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:27:13.344166+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.8062","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PARN: Rating: GREEN; Mode of pathogenicity: None; Publications: 25893599, 26342108, 25848748; Phenotypes: Dyskeratosis congenita, autosomal recessive 6, MIM# 616353, Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, MIM# 616371; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PARN","entity_type":"gene"},{"created":"2021-06-18T09:27:03.604785+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.285","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PARN as ready","entity_name":"PARN","entity_type":"gene"}]}