{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1947","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1945","results":[{"created":"2020-02-02T14:34:20.750068+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1158","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ATAD3A.","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:29:17.246033+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1916","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATAD3A as ready","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:29:17.235465+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1916","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad3a has been classified as Green List (High Evidence).","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:29:01.308626+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1916","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATAD3A were changed from  to Harel-Yoon syndrome, MIM# 617183","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:28:29.168658+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1915","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATAD3A were set to ","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:28:20.100406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1158","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 27640307, 32004445; Phenotypes: Harel-Yoon syndrome, MIM# 617183; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:27:33.971472+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1914","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATAD3A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:26:52.914441+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1913","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ATAD3A.","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:26:24.051441+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1913","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 27640307, 32004445; Phenotypes: Harel-Yoon syndrome, MIM# 617183; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:25:50.534121+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATAD3A as ready","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:25:50.523285+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad3a has been classified as Green List (High Evidence).","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:24:56.248025+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATAD3A were changed from  to Harel-Yoon syndrome, MIM# 617183","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:24:14.691623+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATAD3A were set to ","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:23:38.275723+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATAD3A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:23:03.086893+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ATAD3A.","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:22:52.510566+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 27640307, 32004445; Phenotypes: Harel-Yoon syndrome 617183; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ATAD3A","entity_type":"gene"},{"created":"2020-02-02T14:18:56.707199+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYOM1 as ready","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:18:56.696633+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myom1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:18:31.793187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1158","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYOM1 as ready","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:18:31.782675+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1158","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myom1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:18:20.599129+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1158","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYOM1 were changed from  to Hypertrophic cardiomyopathy","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:17:58.187176+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1157","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYOM1 were set to ","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:17:05.315907+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1156","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYOM1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:16:44.887310+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1155","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYOM1 as Amber List (moderate evidence)","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:16:44.876282+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1155","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myom1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:16:38.480095+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYOM1 were changed from  to Hypertrophic cardiomyopathy","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:16:04.485746+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1154","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYOM1: Rating: AMBER; Mode of pathogenicity: None; Publications: 27600940, 26656175, 21256114; Phenotypes: Hypertrophic cardiomyopathy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:16:00.709127+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYOM1 were set to ","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:13:18.798986+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYOM1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:12:41.792359+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYOM1 as Amber List (moderate evidence)","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:12:41.782039+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myom1 has been classified as Amber List (Moderate Evidence).","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-02T14:11:58.792066+11:00","panel_name":"Hypertrophic cardiomyopathy_HCM","panel_id":111,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYOM1: Rating: AMBER; Mode of pathogenicity: None; Publications: 27600940, 26656175, 21256114; Phenotypes: Hypertrophic cardiomyopathy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOM1","entity_type":"gene"},{"created":"2020-02-01T21:33:24.946720+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1913","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPM3 as ready","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:33:24.936325+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1913","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpm3 has been classified as Red List (Low Evidence).","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:33:11.361090+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1913","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPM3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:32:41.200289+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1912","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:31:57.895695+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1911","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DPM3 were set to ","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:30:42.890869+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1910","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DPM3 were changed from  to Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15 612937","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:27:48.933357+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1909","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DPM3 as Red List (low evidence)","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:27:48.923131+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1909","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpm3 has been classified as Red List (Low Evidence).","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:26:47.015523+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1908","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPM3: Rating: RED; Mode of pathogenicity: None; Publications: 19576565, 28803818, 30931530, 31469168; Phenotypes: Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15 612937; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPM3","entity_type":"gene"},{"created":"2020-02-01T21:20:50.051441+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1908","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPM2 as ready","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:20:50.024636+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1908","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpm2 has been classified as Amber List (Moderate Evidence).","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:19:40.299313+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1908","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DPM2 were changed from  to Congenital disorder of glycosylation, type Iu, MIM#615042","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:18:41.742574+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1907","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DPM2 were set to ","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:17:20.853889+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1906","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:16:46.681532+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1905","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DPM2 as Amber List (moderate evidence)","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:16:46.670806+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1905","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpm2 has been classified as Amber List (Moderate Evidence).","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:16:05.482820+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1904","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPM2: Rating: AMBER; Mode of pathogenicity: None; Publications: 23109149; Phenotypes: Congenital disorder of glycosylation, type Iu, MIM#615042; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPM2","entity_type":"gene"},{"created":"2020-02-01T21:06:38.560586+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1904","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC3 as ready","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:06:38.550229+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1904","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc3 has been classified as Red List (Low Evidence).","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:06:17.531852+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1904","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAJC3 were changed from  to Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, MIM# 616192","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:05:37.038743+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1903","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAJC3 were set to ","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:04:56.590620+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1902","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAJC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:02:45.327603+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1901","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJC3 as Red List (low evidence)","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:02:45.316984+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1901","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc3 has been classified as Red List (Low Evidence).","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T21:02:06.800276+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1900","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAJC3: Rating: RED; Mode of pathogenicity: None; Publications: 25466870, 28940199; Phenotypes: Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, MIM# 616192; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAJC3","entity_type":"gene"},{"created":"2020-02-01T20:54:32.911836+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1900","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: DMPK.","entity_name":"DMPK","entity_type":"gene"},{"created":"2020-02-01T20:53:39.797273+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1900","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG4 as ready","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:53:39.786484+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1900","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Green List (High Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:47:43.151817+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1154","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLG4 were changed from  to Intellectual disability; Marfanoid habitus","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:47:23.090573+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1153","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLG4 were set to ","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:46:59.476148+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1152","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DLG4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:46:35.193801+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1151","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Green List (high evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:46:35.182940+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Green List (High Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:46:14.898258+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1150","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DLG4: Added comment: Four unrelated individuals reported.; Changed rating: GREEN; Changed publications: 27479843, 25123844, 19617690, 29460436, 23020937, 28135719; Changed phenotypes: Intellectual disability, Marfanoid habitus; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Set current diagnostic: yes","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:44:33.161937+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1900","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLG4 were changed from  to Intellectual disability; Marfanoid habitus","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:44:00.325124+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1899","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLG4 were set to ","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:41:08.216083+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1898","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DLG4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:39:56.525872+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1897","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Green List (high evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:39:56.515358+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1897","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Green List (High Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:37:45.426596+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1896","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DLG4: Added comment: Four unrelated individuals reported.; Changed rating: GREEN; Changed publications: 27479843, 25123844, 19617690, 29460436, 23020937, 28135719; Changed phenotypes: Intellectual disability, Marfanoid habitus; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Set current diagnostic: yes","entity_name":"DLG4","entity_type":"gene"},{"created":"2020-02-01T20:32:33.993179+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1896","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLAT as Amber List (moderate evidence)","entity_name":"DLAT","entity_type":"gene"},{"created":"2020-02-01T20:32:33.983010+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1896","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlat has been classified as Amber List (Moderate Evidence).","entity_name":"DLAT","entity_type":"gene"},{"created":"2020-02-01T20:31:52.714930+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1895","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DLAT: Added comment: Only two families with ID reported; third individual had paroxysmal dyskinesia.; Changed rating: AMBER; Changed publications: 16049940, 29093066","entity_name":"DLAT","entity_type":"gene"},{"created":"2020-02-01T20:31:26.645618+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1150","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIP2B as ready","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:31:26.635256+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dip2b has been classified as Amber List (Moderate Evidence).","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:31:13.516335+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1150","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIP2B were changed from  to Mental retardation, FRA12A type, MIM# 136630","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:30:38.551500+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1149","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIP2B were set to ","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:30:16.781153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1148","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: DIP2B was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:29:55.818841+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1147","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIP2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:29:30.778056+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1146","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DIP2B as Amber List (moderate evidence)","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:29:30.767726+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1146","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dip2b has been classified as Amber List (Moderate Evidence).","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:29:09.591830+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1145","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DIP2B: Rating: AMBER; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 17236128; Phenotypes: Mental retardation, FRA12A type, MIM# 136630; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:27:41.942884+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1895","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIP2B as ready","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:27:41.932255+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1895","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dip2b has been classified as Amber List (Moderate Evidence).","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:27:20.707793+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1895","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIP2B were changed from  to Mental retardation, FRA12A type, MIM# 136630","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:26:46.088031+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1894","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIP2B were set to ","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:26:11.487719+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1893","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: DIP2B was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:25:25.234692+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1892","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIP2B was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:22:26.338697+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1891","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIP2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:21:28.335060+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1890","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DIP2B as Amber List (moderate evidence)","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:21:28.324738+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1890","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dip2b has been classified as Amber List (Moderate Evidence).","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:20:48.825214+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Tag 5'UTR tag was added to gene: DIP2B.","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:20:38.616489+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DIP2B: Rating: AMBER; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 17236128; Phenotypes: Mental retardation, FRA12A type, MIM# 136630; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIP2B","entity_type":"gene"},{"created":"2020-02-01T20:16:56.348355+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DENND5A as ready","entity_name":"DENND5A","entity_type":"gene"},{"created":"2020-02-01T20:16:56.336022+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dennd5a has been classified as Green List (High Evidence).","entity_name":"DENND5A","entity_type":"gene"},{"created":"2020-02-01T20:16:39.479891+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DENND5A as Green List (high evidence)","entity_name":"DENND5A","entity_type":"gene"},{"created":"2020-02-01T20:16:39.455797+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dennd5a has been classified as Green List (High Evidence).","entity_name":"DENND5A","entity_type":"gene"},{"created":"2020-02-01T20:15:56.788427+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1888","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DENND5A was added\ngene: DENND5A was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: DENND5A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DENND5A were set to 27431290; 27866705\nPhenotypes for gene: DENND5A were set to Epileptic encephalopathy, early infantile, 49, MIM#\t617281\nReview for gene: DENND5A was set to GREEN\nAdded comment: Four unrelated families, ID is part of the phenotype. \nSources: Expert list","entity_name":"DENND5A","entity_type":"gene"}]}