{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1948","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1946","results":[{"created":"2020-02-01T19:52:50.842511+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1145","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCPS as ready","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:52:50.832379+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcps has been classified as Green List (High Evidence).","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:52:32.963671+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1145","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCPS as Green List (high evidence)","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:52:32.953473+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcps has been classified as Green List (High Evidence).","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:52:12.563418+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1144","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DCPS was added\ngene: DCPS was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: DCPS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DCPS were set to 25701870; 30289615; 25712129\nPhenotypes for gene: DCPS were set to Al-Raqad syndrome, MIM#616459\nReview for gene: DCPS was set to GREEN\ngene: DCPS was marked as current diagnostic\nAdded comment: 7 individuals from 3 families reported. \nSources: Expert list","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:50:06.943737+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1887","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCPS as ready","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:50:06.932990+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1887","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcps has been classified as Green List (High Evidence).","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:44:52.013579+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1887","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCPS as Green List (high evidence)","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:44:51.962861+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1887","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcps has been classified as Green List (High Evidence).","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:44:06.736991+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1886","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DCPS was added\ngene: DCPS was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: DCPS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DCPS were set to 25701870; 30289615; 25712129\nPhenotypes for gene: DCPS were set to Al-Raqad syndrome, MIM#616459\nReview for gene: DCPS was set to GREEN\ngene: DCPS was marked as current diagnostic\nAdded comment: 7 individuals from 3 families reported. \nSources: Expert list","entity_name":"DCPS","entity_type":"gene"},{"created":"2020-02-01T19:36:47.502136+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCC as ready","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T19:36:47.491959+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcc has been classified as Green List (High Evidence).","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T19:36:42.887137+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCC were changed from  to Agenesis of the corpus callosum","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T19:36:04.818018+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCC were set to ","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T19:35:28.883568+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DCC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T19:34:50.721264+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DCC: Rating: GREEN; Mode of pathogenicity: None; Publications: 31697046; Phenotypes: Agenesis of the corpus callosum; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCC","entity_type":"gene"},{"created":"2020-02-01T18:35:40.130764+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1885","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CWF19L1 as ready","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-02-01T18:35:40.119848+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1885","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cwf19l1 has been classified as Green List (High Evidence).","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-02-01T18:35:28.980181+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1885","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CWF19L1 as Green List (high evidence)","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-02-01T18:35:28.956162+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1885","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cwf19l1 has been classified as Green List (High Evidence).","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-02-01T18:33:59.109921+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1884","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CWF19L1 was added\ngene: CWF19L1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: CWF19L1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CWF19L1 were set to 25361784; 15981765; 26197978; 27016154; 30167849\nPhenotypes for gene: CWF19L1 were set to Spinocerebellar ataxia, autosomal recessive 17, MIM#616127; intellectual disability, developmental delay\nReview for gene: CWF19L1 was set to GREEN\ngene: CWF19L1 was marked as current diagnostic\nAdded comment: Three unrelated families reported, ID is part of the phenotype. \nSources: Expert list","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-02-01T18:28:32.446640+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1143","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CUX1 as ready","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:28:32.435983+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1143","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cux1 has been classified as Green List (High Evidence).","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:28:19.927407+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1143","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CUX1 as Green List (high evidence)","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:28:19.917347+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1143","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cux1 has been classified as Green List (High Evidence).","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:27:51.233091+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1142","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CUX1 was added\ngene: CUX1 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: CUX1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: CUX1 were set to 25059644; 20510857; 30014507\nPhenotypes for gene: CUX1 were set to Global developmental delay with or without impaired intellectual development, 618330\nReview for gene: CUX1 was set to GREEN\ngene: CUX1 was marked as current diagnostic\nAdded comment: Nine individuals from 7 families reported. Three individuals had normal intelligence at school age despite significant early developmental delay. \nSources: Expert list","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:27:24.430650+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1883","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CUX1 as ready","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:27:24.420393+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1883","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cux1 has been classified as Green List (High Evidence).","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:26:01.355361+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1883","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CUX1 as Green List (high evidence)","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:26:01.331133+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1883","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cux1 has been classified as Green List (High Evidence).","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:25:20.997310+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1882","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CUX1 was added\ngene: CUX1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: CUX1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: CUX1 were set to 25059644; 20510857; 30014507\nPhenotypes for gene: CUX1 were set to Global developmental delay with or without impaired intellectual development, MIM#618330\nReview for gene: CUX1 was set to GREEN\ngene: CUX1 was marked as current diagnostic\nAdded comment: Nine individuals from 7 families reported. Three individuals had normal intelligence at school age despite significant early developmental delay. \nSources: Expert list","entity_name":"CUX1","entity_type":"gene"},{"created":"2020-02-01T18:11:44.040677+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1881","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRBN as ready","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T18:11:44.028609+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1881","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crbn has been classified as Amber List (Moderate Evidence).","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T18:11:31.384811+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1881","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRBN were changed from  to Mental retardation, autosomal recessive 2, MIM# 607417","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T17:40:36.172948+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1880","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRBN were set to ","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T17:39:53.901591+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1879","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CRBN as Amber List (moderate evidence)","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T17:39:53.891303+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1879","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crbn has been classified as Amber List (Moderate Evidence).","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T17:39:12.763211+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1878","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRBN: Rating: AMBER; Mode of pathogenicity: None; Publications: 15557513, 28143899; Phenotypes: Mental retardation, autosomal recessive 2, MIM# 607417; Mode of inheritance: None","entity_name":"CRBN","entity_type":"gene"},{"created":"2020-02-01T17:27:45.772735+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1878","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ9 as Amber List (moderate evidence)","entity_name":"COQ9","entity_type":"gene"},{"created":"2020-02-01T17:27:45.762247+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1878","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq9 has been classified as Amber List (Moderate Evidence).","entity_name":"COQ9","entity_type":"gene"},{"created":"2020-02-01T17:27:05.594558+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1877","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: COQ9: Added comment: Reviewed again: severe neonatal presentation with metabolic decompensation, including neurological features such as abnormal tone and seizures, but not intellectual disability as such. Downgrade to Amber on this panel.; Changed rating: AMBER","entity_name":"COQ9","entity_type":"gene"},{"created":"2020-02-01T17:22:21.404826+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1877","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ2 as Amber List (moderate evidence)","entity_name":"COQ2","entity_type":"gene"},{"created":"2020-02-01T17:22:21.394243+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1877","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq2 has been classified as Amber List (Moderate Evidence).","entity_name":"COQ2","entity_type":"gene"},{"created":"2020-02-01T17:21:40.940598+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: COQ2: Added comment: On further review of the literature, there is poor documentation of intellectual disability as such in the molecularly confirmed cases. Presentation is much more commonly with renal or multi-system disease.; Changed rating: AMBER","entity_name":"COQ2","entity_type":"gene"},{"created":"2020-02-01T16:56:05.047018+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL1A2 as ready","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:56:05.036644+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col1a2 has been classified as Red List (Low Evidence).","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:55:35.647790+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COLEC10 as ready","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:55:35.637417+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: colec10 has been classified as Red List (Low Evidence).","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:55:23.242846+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1876","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COLEC10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:54:32.879426+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1875","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COLEC10 were changed from  to 3MC syndrome 3, MIM# 248340","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:53:58.688071+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1874","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COLEC10 were set to ","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:53:14.369992+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1873","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COLEC10 as Red List (low evidence)","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:53:14.359403+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1873","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: colec10 has been classified as Red List (Low Evidence).","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:52:38.027715+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1872","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COLEC10: Rating: RED; Mode of pathogenicity: None; Publications: 28301481; Phenotypes: 3MC syndrome 3, MIM# 248340; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COLEC10","entity_type":"gene"},{"created":"2020-02-01T16:48:46.454679+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1872","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL1A2 were changed from  to Ehlers-Danlos syndrome, arthrochalasia type, 2, MIM# 617821; Ehlers-Danlos syndrome, cardiac valvular type, MIM# 225320; Osteogenesis imperfecta, type II, MIM# 166210; Osteogenesis imperfecta, type III, MIM# 259420; Osteogenesis imperfecta, type IV, MIM# 166220","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:37:07.608535+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1871","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL1A2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:37:02.652890+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COA3 as ready","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:37:02.640481+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:36:23.970209+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1870","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COL1A2 as Red List (low evidence)","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:36:23.959954+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1870","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col1a2 has been classified as Red List (Low Evidence).","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:35:42.961936+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1869","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL1A2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ehlers-Danlos syndrome, arthrochalasia type, 2, MIM# 617821, Ehlers-Danlos syndrome, cardiac valvular type, MIM# 225320, Osteogenesis imperfecta, type II, MIM# 166210, Osteogenesis imperfecta, type III, MIM# 259420, Osteogenesis imperfecta, type IV, MIM# 166220; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"COL1A2","entity_type":"gene"},{"created":"2020-02-01T16:31:53.121317+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1141","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COA3 as ready","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:31:53.110967+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1141","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:24:41.321712+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COA3 were changed from  to Mitochondrial complex IV deficiency","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:24:23.529341+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1141","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COA3 were changed from  to Mitochondrial complex IV deficiency","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:23:42.834981+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1140","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COA3 were set to ","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:23:24.640264+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1139","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COA3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:23:06.838187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1138","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COA3 as Red List (low evidence)","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:23:06.817568+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1138","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:22:57.140329+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COA3 were set to ","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:22:44.382852+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1137","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COA3: Rating: RED; Mode of pathogenicity: None; Publications: 25604084; Phenotypes: Mitochondrial complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:22:11.773977+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COA3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:21:34.056012+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COA3 as Red List (low evidence)","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:21:34.045728+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:20:57.428635+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COA3: Rating: RED; Mode of pathogenicity: None; Publications: 25604084; Phenotypes: Mitochondrial complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:20:12.506422+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1869","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COA3 were changed from Mitochondrial complex IV deficiency to Mitochondrial complex IV deficiency","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:20:02.429480+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1869","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COA3 as ready","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:20:02.416914+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1869","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:19:44.637058+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1869","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COA3 were set to 25604084","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:19:18.635804+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COA3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:18:47.896056+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COA3 were changed from  to Mitochondrial complex IV deficiency","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:18:21.515872+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COA3 were set to ","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:17:59.024274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNTN3 as ready","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:17:58.948849+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntn3 has been classified as Red List (Low Evidence).","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:17:55.086554+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1868","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COA3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:17:27.264868+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1867","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COA3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:16:56.657324+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1867","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNTN3 were set to ","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:16:27.119632+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1867","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COA3 as Red List (low evidence)","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:16:27.108624+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1867","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coa3 has been classified as Red List (Low Evidence).","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:15:45.895665+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1866","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COA3: Rating: RED; Mode of pathogenicity: None; Publications: 25604084; Phenotypes: Mitochondrial complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COA3","entity_type":"gene"},{"created":"2020-02-01T16:14:02.569683+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1866","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CNTN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:10:33.923686+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1137","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNTN3 as ready","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:10:33.913123+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntn3 has been classified as Red List (Low Evidence).","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:10:22.170517+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1137","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNTN3 were changed from  to Intellectual disability","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:09:59.205886+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1136","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNTN3 were set to ","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:09:38.006704+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1135","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CNTN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:07:54.668320+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1134","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CNTN3 as Red List (low evidence)","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:07:54.657758+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntn3 has been classified as Red List (Low Evidence).","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:07:33.991072+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1133","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CNTN3: Rating: RED; Mode of pathogenicity: None; Publications: 28600779; Phenotypes: Intellectual disability; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNTN3","entity_type":"gene"},{"created":"2020-02-01T16:05:09.457883+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1865","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CNTN3 as Red List (low evidence)","entity_name":"CNTN3","entity_type":"gene"}]}