{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1946","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1944","results":[{"created":"2020-02-03T12:31:45.374256+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHST8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHST8","entity_type":"gene"},{"created":"2020-02-03T12:31:08.537783+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHST8 as Red List (low evidence)","entity_name":"CHST8","entity_type":"gene"},{"created":"2020-02-03T12:31:08.527082+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chst8 has been classified as Red List (Low Evidence).","entity_name":"CHST8","entity_type":"gene"},{"created":"2020-02-03T12:01:59.609721+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.29","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: CHST8: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 22289416, 28204496; Phenotypes: Peeling Skin Syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHST8","entity_type":"gene"},{"created":"2020-02-03T10:39:58.605008+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1177","user_name":"Sebastian Lunke","item_type":"entity","text":"Marked gene: RASA2 as ready","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:39:58.595034+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1177","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:39:33.124332+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1177","user_name":"Sebastian Lunke","item_type":"entity","text":"Mode of inheritance for gene: RASA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:39:01.420801+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.14","user_name":"Sebastian Lunke","item_type":"entity","text":"Marked gene: RASA2 as ready","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:39:01.402657+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.14","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Red List (Low Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:38:53.723393+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1176","user_name":"Sebastian Lunke","item_type":"entity","text":"Classified gene: RASA2 as Amber List (moderate evidence)","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:38:53.712164+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1176","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:38:39.023089+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.14","user_name":"Sebastian Lunke","item_type":"entity","text":"Publications for gene: RASA2 were set to ","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:38:24.391731+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.11","user_name":"Sebastian Lunke","item_type":"entity","text":"Publications for gene: RASA2 were set to 25049390; 25049390","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:38:18.596985+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1175","user_name":"Sebastian Lunke","item_type":"entity","text":"reviewed gene: RASA2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25049390, 30311384; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:37:21.647982+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.13","user_name":"Sebastian Lunke","item_type":"entity","text":"Classified gene: RASA2 as Red List (low evidence)","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:37:21.637304+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.13","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Red List (Low Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:36:25.958803+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.12","user_name":"Sebastian Lunke","item_type":"entity","text":"reviewed gene: RASA2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:35:21.182731+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.10","user_name":"Sebastian Lunke","item_type":"entity","text":"Marked gene: RASA2 as ready","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:35:21.172310+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.10","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:34:55.709432+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.10","user_name":"Sebastian Lunke","item_type":"entity","text":"Publications for gene: RASA2 were set to ","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:34:27.303746+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.9","user_name":"Sebastian Lunke","item_type":"entity","text":"Mode of inheritance for gene: RASA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:33:56.610165+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.8","user_name":"Sebastian Lunke","item_type":"entity","text":"Classified gene: RASA2 as Amber List (moderate evidence)","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:33:56.599156+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.8","user_name":"Sebastian Lunke","item_type":"entity","text":"Gene: rasa2 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T10:33:05.184240+11:00","panel_name":"Rasopathy","panel_id":164,"panel_version":"0.7","user_name":"Sebastian Lunke","item_type":"entity","text":"reviewed gene: RASA2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25049390, 25049390; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RASA2","entity_type":"gene"},{"created":"2020-02-03T09:32:04.369029+11:00","panel_name":"Long QT Syndrome","panel_id":131,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Both mono allelic and biallelic variants cause disease, no evidence for imprinting.; to: Both mono allelic and biallelic variants cause disease; excess of maternally inherited variants observed in LongQT syndrome likely linked to imprinting at this locus.","entity_name":"KCNQ1","entity_type":"gene"},{"created":"2020-02-02T22:14:23.930208+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1175","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TKFC as ready","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:14:23.920274+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:14:09.953620+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1175","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TKFC as Amber List (moderate evidence)","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:14:09.943443+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:13:48.281512+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1174","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TKFC was added\ngene: TKFC was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: TKFC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TKFC were set to 32004446\nPhenotypes for gene: TKFC were set to Developmental delay; cataracts; liver dysfunction\nReview for gene: TKFC was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:13:43.796225+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1940","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TKFC as ready","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:13:43.784416+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1940","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:11:53.671943+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TKFC as ready","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:11:53.661490+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:11:48.172819+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TKFC as Amber List (moderate evidence)","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:11:48.162971+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:11:10.576417+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TKFC was added\ngene: TKFC was added to Cataract. Sources: Literature\nMode of inheritance for gene: TKFC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TKFC were set to 32004446\nPhenotypes for gene: TKFC were set to Developmental delay; cataracts; liver dysfunction\nReview for gene: TKFC was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:10:50.437462+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1940","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TKFC as Amber List (moderate evidence)","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:10:50.425678+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1940","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tkfc has been classified as Amber List (Moderate Evidence).","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:09:51.104809+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1939","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TKFC was added\ngene: TKFC was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: TKFC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TKFC were set to 32004446\nPhenotypes for gene: TKFC were set to Developmental delay; cataracts; liver dysfunction\nReview for gene: TKFC was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature","entity_name":"TKFC","entity_type":"gene"},{"created":"2020-02-02T22:02:46.916932+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RALGAPA1 as ready","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T22:02:46.906663+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T22:02:41.490489+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RALGAPA1 as Green List (high evidence)","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T22:02:41.466320+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.559","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T22:02:03.634555+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.558","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RALGAPA1 was added\ngene: RALGAPA1 was added to Genetic Epilepsy. Sources: Literature\nMode of inheritance for gene: RALGAPA1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RALGAPA1 were set to 32004447\nPhenotypes for gene: RALGAPA1 were set to Intellectual disability; hypotonia; infantile spasms.\nReview for gene: RALGAPA1 was set to GREEN\nAdded comment: Four unrelated individuals reported. \nSources: Literature","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:59:29.510748+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1173","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RALGAPA1 as ready","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:59:29.500434+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:59:18.766941+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1173","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RALGAPA1 as Green List (high evidence)","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:59:18.756699+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:58:57.371418+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1172","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RALGAPA1 was added\ngene: RALGAPA1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: RALGAPA1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RALGAPA1 were set to 32004447\nPhenotypes for gene: RALGAPA1 were set to Intellectual disability; hypotonia; infantile spasms.\nReview for gene: RALGAPA1 was set to GREEN\nAdded comment: Four unrelated individuals reported. \nSources: Literature","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:58:34.093813+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1938","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RALGAPA1 as ready","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:58:34.083341+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1938","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:57:26.343784+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1938","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RALGAPA1 as Green List (high evidence)","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:57:26.319979+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1938","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ralgapa1 has been classified as Green List (High Evidence).","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T21:55:13.837103+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1937","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RALGAPA1 was added\ngene: RALGAPA1 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: RALGAPA1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RALGAPA1 were set to 32004447\nPhenotypes for gene: RALGAPA1 were set to Intellectual disability; hypotonia; infantile spasms.\nReview for gene: RALGAPA1 was set to GREEN\nAdded comment: Four unrelated individuals reported. \nSources: Literature","entity_name":"RALGAPA1","entity_type":"gene"},{"created":"2020-02-02T20:06:33.170287+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1936","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FDXR as ready","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T20:06:33.159959+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1936","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdxr has been classified as Red List (Low Evidence).","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T20:06:16.696351+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1936","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FDXR were changed from  to Auditory neuropathy and optic atrophy, MIM# 617717","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T20:05:34.902014+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1935","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FDXR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T20:04:35.701463+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1934","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FDXR as Red List (low evidence)","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T20:04:35.690122+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1934","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdxr has been classified as Red List (Low Evidence).","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T19:57:38.077280+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1933","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGF14: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spinocerebellar ataxia 27, MIM# 609307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF14","entity_type":"gene"},{"created":"2020-02-02T19:52:43.023797+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1933","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FDXR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Auditory neuropathy and optic atrophy, MIM# 617717; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FDXR","entity_type":"gene"},{"created":"2020-02-02T19:28:13.911549+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1933","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCG as ready","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:28:13.901268+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1933","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancg has been classified as Amber List (Moderate Evidence).","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:27:25.337467+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1933","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCG were changed from  to Fanconi anemia, complementation group G, MIM# 614082","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:26:18.439484+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1932","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCB as ready","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:26:18.429033+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1932","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancb has been classified as Amber List (Moderate Evidence).","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:26:15.222948+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1932","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:25:50.335140+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1931","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCB were changed from  to Fanconi anemia, complementation group B, MIM# 300514","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:25:21.245699+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1931","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCG as Amber List (moderate evidence)","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:25:21.234943+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1931","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancg has been classified as Amber List (Moderate Evidence).","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:24:38.329427+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1930","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FANCG: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anemia, complementation group G, MIM# 614082; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-02-02T19:23:18.825398+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1930","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:22:45.366470+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1929","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCD2 as Amber List (moderate evidence)","entity_name":"FANCD2","entity_type":"gene"},{"created":"2020-02-02T19:22:45.356363+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1929","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancd2 has been classified as Amber List (Moderate Evidence).","entity_name":"FANCD2","entity_type":"gene"},{"created":"2020-02-02T19:21:55.860742+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1928","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FANCD2: Added comment: Clinical presentation is typically with congenital abnormalities/BMF. Only ~10% have ID as part of the phenotype.; Changed rating: AMBER","entity_name":"FANCD2","entity_type":"gene"},{"created":"2020-02-02T19:21:03.533731+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1928","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCB as Amber List (moderate evidence)","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:21:03.523455+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1928","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancb has been classified as Amber List (Moderate Evidence).","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T19:20:22.605515+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1927","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FANCB: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anemia, complementation group B, MIM# 300514; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-02-02T15:50:59.397796+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1927","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Intellect normal in xeroderma pigmentosum; mild learning difficulties described in XFE progressed syndrome.; to: Intellect normal in xeroderma pigmentosum; mild learning difficulties described in XFE progeroid syndrome.","entity_name":"ERCC4","entity_type":"gene"},{"created":"2020-02-02T15:49:34.766154+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1927","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPB41L1 as ready","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:49:34.755378+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1927","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epb41l1 has been classified as Red List (Low Evidence).","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:49:09.639319+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1171","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPB41L1 as ready","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:49:09.629206+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epb41l1 has been classified as Red List (Low Evidence).","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:48:55.470979+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1171","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPB41L1 were changed from  to Mental retardation, autosomal dominant 11, MIM# 614257","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:48:36.305492+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1170","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPB41L1 were set to ","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:48:14.279523+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1927","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPB41L1 were changed from  to Mental retardation, autosomal dominant 11, MIM# 614257","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:47:57.495328+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1169","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPB41L1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:47:35.740699+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1168","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EPB41L1 as Red List (low evidence)","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:47:35.730507+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1168","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epb41l1 has been classified as Red List (Low Evidence).","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:47:15.536929+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1167","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EPB41L1: Rating: RED; Mode of pathogenicity: None; Publications: 21376300, 26539891, 25961944; Phenotypes: Mental retardation, autosomal dominant 11, MIM# 614257; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:47:03.687179+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1926","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPB41L1 were set to ","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:46:21.067212+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1925","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPB41L1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:45:31.275556+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1924","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EPB41L1 as Red List (low evidence)","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:45:31.265341+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1924","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epb41l1 has been classified as Red List (Low Evidence).","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:44:44.845989+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1923","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EPB41L1: Rating: RED; Mode of pathogenicity: None; Publications: 21376300, 26539891, 25961944; Phenotypes: Mental retardation, autosomal dominant 11 614257; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPB41L1","entity_type":"gene"},{"created":"2020-02-02T15:16:20.630495+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1167","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMC1 as ready","entity_name":"EMC1","entity_type":"gene"},{"created":"2020-02-02T15:16:20.619934+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1167","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emc1 has been classified as Green List (High Evidence).","entity_name":"EMC1","entity_type":"gene"},{"created":"2020-02-02T15:15:08.887944+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1923","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMG1 as ready","entity_name":"EMG1","entity_type":"gene"}]}