{"count":220380,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1497","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1495","results":[{"created":"2020-11-25T18:09:30.148198+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG8 were changed from  to Congenital disorder of glycosylation, type Ih, MIM# 608104","entity_name":"ALG8","entity_type":"gene"},{"created":"2020-11-25T18:08:55.758005+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG8 were set to ","entity_name":"ALG8","entity_type":"gene"},{"created":"2020-11-25T18:08:21.999846+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG8","entity_type":"gene"},{"created":"2020-11-25T18:07:44.758590+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALG8: Rating: GREEN; Mode of pathogenicity: None; Publications: 26066342; Phenotypes: Congenital disorder of glycosylation, type Ih, MIM# 608104; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG8","entity_type":"gene"},{"created":"2020-11-25T18:01:36.879708+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3211","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALG3 as ready","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T18:01:36.862541+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3211","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alg3 has been classified as Green List (High Evidence).","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T18:01:32.750577+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3211","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG3 were changed from  to Congenital disorder of glycosylation, type Id, MIM# 601110","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T18:00:59.769611+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3210","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG3 were set to ","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T18:00:27.675327+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3209","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:59:50.733818+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3208","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31067009; Phenotypes: Congenital disorder of glycosylation, type Id, MIM# 601110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:59:14.735188+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.918","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALG3 as ready","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:59:14.724430+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.918","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alg3 has been classified as Green List (High Evidence).","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:59:11.064773+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.918","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG3 were changed from  to Congenital disorder of glycosylation, type Id, MIM# 601110","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:58:41.123602+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.917","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG3 were set to ","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:58:11.474601+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.916","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:57:40.761138+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.915","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31067009; Phenotypes: Congenital disorder of glycosylation, type Id, MIM# 601110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:56:51.287016+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5446","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALG3 as ready","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:56:51.276705+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5446","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alg3 has been classified as Green List (High Evidence).","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:56:34.829287+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5446","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG3 were changed from  to Congenital disorder of glycosylation, type Id, MIM# 601110","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:56:04.092579+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5445","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG3 were set to ","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:55:45.393314+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5444","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:55:24.942539+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5443","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31067009; Phenotypes: Congenital disorder of glycosylation, type Id, MIM# 601110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:54:18.010391+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALG3 as ready","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:54:17.997865+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alg3 has been classified as Green List (High Evidence).","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:54:14.131048+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG3 were changed from  to Congenital disorder of glycosylation, type Id, MIM# 601110","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:53:25.562115+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG3 were set to ","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:52:54.708000+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T17:52:23.904704+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"0.192","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31067009; Phenotypes: Congenital disorder of glycosylation, type Id, MIM# 601110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG3","entity_type":"gene"},{"created":"2020-11-25T15:42:48.989846+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5443","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC3A2 were changed from  to Autism","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T15:42:30.722575+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5442","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC3A2 were set to ","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T15:42:10.211829+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC3A2: Rating: RED; Mode of pathogenicity: None; Publications: 31701662; Phenotypes: Autism; Mode of inheritance: None","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T15:17:25.918433+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Naomi Baker","item_type":"entity","text":"changed review comment from: No evidence of mendelian gene-disease association reported in the literature.; to: Weak evidence of mendelian gene-disease association reported in the literature.\r\n\r\nThree monoallelic missense variants reported in patients with Autism spectrum disorder (ASD) from one publication (PMID: 31701662).","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T14:47:35.284269+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC3A2 as ready","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T14:47:35.275985+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc3a2 has been classified as Red List (Low Evidence).","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T14:47:24.516119+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC3A2 as Red List (low evidence)","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T14:47:24.500847+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc3a2 has been classified as Red List (Low Evidence).","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T14:46:49.699880+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5440","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HOXA4 as ready","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:46:49.686009+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5440","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa4 has been classified as Red List (Low Evidence).","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:46:42.477871+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5440","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HOXA4 were set to 33193662","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:46:29.508022+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5439","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HOXA4 were changed from  to Microtia-Atresia; CAKUT","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:46:13.982237+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5438","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HOXA4 were set to ","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:45:50.891194+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5437","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HOXA4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:45:33.905919+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5436","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HOXA4 as Red List (low evidence)","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:45:33.895800+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa4 has been classified as Red List (Low Evidence).","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T14:44:07.478447+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5435","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASTE1 as ready","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:44:07.439657+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5435","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aste1 has been classified as Red List (Low Evidence).","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:43:59.584845+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5435","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASTE1 were changed from  to palmar and plantar fibromatosis","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:43:29.160807+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5434","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ASTE1 were set to ","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:43:02.329566+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5433","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ASTE1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:42:44.351797+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5432","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ASTE1 as Red List (low evidence)","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T14:42:44.340715+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5432","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aste1 has been classified as Red List (Low Evidence).","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T13:53:24.524722+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: SLC3A2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC3A2","entity_type":"gene"},{"created":"2020-11-25T13:36:47.881812+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: HOXA4: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 33193662; Phenotypes: Microtia-Atresia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HOXA4","entity_type":"gene"},{"created":"2020-11-25T12:40:01.209107+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: ASTE1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29104234; Phenotypes: palmar and plantar fibromatosis; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ASTE1","entity_type":"gene"},{"created":"2020-11-25T12:22:22.269998+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCA1 as ready","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:22:22.258076+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarca1 has been classified as Red List (Low Evidence).","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:22:15.381164+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5431","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCA1 were changed from  to Intellectual disability","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:21:51.614646+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5430","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMARCA1 were set to ","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:21:33.389826+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5429","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMARCA1 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":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:21:14.772376+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5428","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMARCA1 as Red List (low evidence)","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:21:14.761618+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5428","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarca1 has been classified as Red List (Low Evidence).","entity_name":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T12:18:59.663128+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5427","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDKAL1 as ready","entity_name":"CDKAL1","entity_type":"gene"},{"created":"2020-11-25T12:18:59.652373+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5427","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdkal1 has been classified as Red List (Low Evidence).","entity_name":"CDKAL1","entity_type":"gene"},{"created":"2020-11-25T12:18:50.792954+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5427","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDKAL1 as Red List (low evidence)","entity_name":"CDKAL1","entity_type":"gene"},{"created":"2020-11-25T12:18:50.782019+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5427","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdkal1 has been classified as Red List (Low Evidence).","entity_name":"CDKAL1","entity_type":"gene"},{"created":"2020-11-25T12:18:03.338275+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5426","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCHH as ready","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:18:03.330250+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tchh has been classified as Red List (Low Evidence).","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:17:56.445083+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5426","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCHH were changed from  to Uncombable hair syndrome 3 MIM#617252","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:17:37.125080+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5425","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCHH were set to ","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:17:19.026127+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5424","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCHH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:17:02.369945+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5423","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TCHH as Red List (low evidence)","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:17:02.358913+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5423","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tchh has been classified as Red List (Low Evidence).","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:14:43.934313+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: TCHH: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 27866708; Phenotypes: Uncombable hair syndrome 3 MIM#617252; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCHH","entity_type":"gene"},{"created":"2020-11-25T12:02:30.966512+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: CDKAL1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"CDKAL1","entity_type":"gene"},{"created":"2020-11-25T11:57:49.205554+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRTAP as ready","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T11:57:49.194119+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crtap has been classified as Green List (High Evidence).","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T11:57:42.704958+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRTAP were changed from  to Osteogenesis imperfecta, type VII MIM#610682","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T11:57:11.825819+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRTAP were set to ","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T11:42:44.306319+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Naomi Baker","item_type":"entity","text":"reviewed gene: SMARCA1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 26740508, 26539891, 29249292.; Phenotypes: ; 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":"SMARCA1","entity_type":"gene"},{"created":"2020-11-25T10:00:13.491220+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRTAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:59:43.772555+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRTAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 21955071, 19846465, 17192541; Phenotypes: Osteogenesis imperfecta, type VII MIM#610682; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:58:41.627281+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRTAP as ready","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:58:41.619181+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crtap has been classified as Green List (High Evidence).","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:58:39.174926+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRTAP were changed from  to Osteogenesis imperfecta, type VII MIM#610682","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:58:09.443595+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRTAP were set to ","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:57:38.542734+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRTAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:56:48.752960+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRTAP as ready","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:56:48.742474+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crtap has been classified as Green List (High Evidence).","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:56:42.226009+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5422","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRTAP were changed from  to Osteogenesis imperfecta, type VII MIM#610682","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:56:20.739826+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5421","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRTAP were set to ","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:55:57.940908+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5420","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRTAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CRTAP","entity_type":"gene"},{"created":"2020-11-25T09:46:15.413028+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3208","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USP9X as ready","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:46:15.401844+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3208","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: usp9x has been classified as Green List (High Evidence).","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:46:00.862078+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3208","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USP9X were changed from  to Mental retardation, X-linked 99, XLR (MIM#300919) and XLD (MIM#300968)","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:45:27.699428+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3207","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USP9X were set to ","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:44:22.405663+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3206","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: USP9X 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":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:43:13.386057+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5419","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USP9X as ready","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:43:13.377964+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5419","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: usp9x has been classified as Green List (High Evidence).","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:43:04.328397+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5419","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USP9X were changed from  to Mental retardation, X-linked 99, XLR (MIM#300919) and XLD (MIM#300968)","entity_name":"USP9X","entity_type":"gene"},{"created":"2020-11-25T09:42:44.697909+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5418","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USP9X were set to ","entity_name":"USP9X","entity_type":"gene"}]}