{"count":220842,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1610","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1608","results":[{"created":"2020-09-04T08:19:33.771465+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.231","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TDRD7 were set to 28837160; 21436445","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:19:06.134721+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TDRD7: Added comment: PMID: 32420594 (2020) - Knockout mouse model recapitulates human cataracts phenotype and provides supporting functional data.; Changed publications: 28837160, 21436445, 32420594; Changed phenotypes: Cataract 36, 613887, glaucoma, nonobstructive azoospermia, arrested spermatogenesis","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:17:54.954112+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4195","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TDRD7 as ready","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:17:54.941519+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4195","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tdrd7 has been classified as Green List (High Evidence).","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:17:47.465412+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4195","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TDRD7 were changed from Cataract 36\t613887; glaucoma; nonobstructive azoospermia; arrested spermatogenesis to Cataract 36,\t613887; glaucoma; nonobstructive azoospermia; arrested spermatogenesis","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:17:19.518388+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4194","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TDRD7 were set to 28837160; 21436445","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:15:51.731833+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4193","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TDRD7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cataract 36, MIM# 613887; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-04T08:14:16.802738+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2949","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAK3 as ready","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:14:16.791777+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2949","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pak3 has been classified as Green List (High Evidence).","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:14:12.292527+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2949","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAK3 were changed from  to Mental retardation, X-linked 30/47, MIM# 300558; Intellectual disability","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:13:36.449938+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2948","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAK3 were set to ","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:13:04.333629+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2947","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAK3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:11:07.355979+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAK3 as ready","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:11:07.345013+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pak3 has been classified as Green List (High Evidence).","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:10:58.723726+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2946","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAK3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9731525, 10946356, 12884430, 17853471, 18523455, 32050918, 32005903, 31943058, 31843706, 31678216; Phenotypes: Mental retardation, X-linked 30/47, MIM# 300558, Intellectual disability; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:10:22.303654+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4193","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAK3 were changed from  to Mental retardation, X-linked 30/47, MIM# 300558; Intellectual disability","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:09:58.804075+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4192","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAK3 were set to ","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:09:13.162200+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4191","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAK3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-04T08:08:56.295248+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAK3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9731525, 10946356, 12884430, 17853471, 18523455, 32050918, 32005903, 31943058, 31843706, 31678216; Phenotypes: Mental retardation, X-linked 30/47, MIM# 300558; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-03T22:02:34.325573+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Arina Puzriakova","item_type":"entity","text":"reviewed gene: CFL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 32160286; Phenotypes: Nemaline myopathy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CFL2","entity_type":"gene"},{"created":"2020-09-03T21:48:20.954221+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Arina Puzriakova","item_type":"entity","text":"reviewed gene: TDRD7: Rating: GREEN; Mode of pathogenicity: None; Publications: 32420594; Phenotypes: Congenital cataracts; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TDRD7","entity_type":"gene"},{"created":"2020-09-03T21:03:58.448142+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2946","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLTC as ready","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:03:58.437018+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2946","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cltc has been classified as Green List (High Evidence).","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:03:54.413141+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2946","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLTC were changed from  to Mental retardation, autosomal dominant 56, MIM# 617854","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:03:35.116405+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2945","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLTC were set to ","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:03:07.646712+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2944","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLTC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:02:39.277707+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2943","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLTC: Rating: GREEN; Mode of pathogenicity: None; Publications: 29100083, 26822784; Phenotypes: Mental retardation, autosomal dominant 56, MIM# 617854; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:02:00.543373+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLTC as ready","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:02:00.533978+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cltc has been classified as Green List (High Evidence).","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:01:57.695017+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLTC were changed from  to Mental retardation, autosomal dominant 56, MIM# 617854","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:01:34.632217+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.833","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLTC were set to ","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:01:05.957479+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.832","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLTC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T21:00:37.146405+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.831","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLTC: Rating: GREEN; Mode of pathogenicity: None; Publications: 29100083, 26822784; Phenotypes: Mental retardation, autosomal dominant 56, MIM# 617854; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:59:40.163259+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLTC as ready","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:59:40.153841+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cltc has been classified as Green List (High Evidence).","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:59:31.385925+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4190","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLTC were changed from  to Mental retardation, autosomal dominant 56, MIM# 617854","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:59:05.561623+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4189","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLTC were set to ","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:58:45.618602+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4188","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLTC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:58:27.579106+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLTC: Rating: GREEN; Mode of pathogenicity: None; Publications: 29100083, 26822784; Phenotypes: Mental retardation, autosomal dominant 56, MIM# 617854; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:56:18.428174+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.440","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLTC as ready","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:56:18.419768+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.440","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cltc has been classified as Amber List (Moderate Evidence).","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:56:13.671472+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.440","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLTC were changed from  to Mental retardation, autosomal dominant 56 (MIM#617854)","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:55:45.441233+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.439","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLTC were set to ","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:55:16.470284+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.438","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLTC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:54:59.547174+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.437","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLTC as Amber List (moderate evidence)","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:54:59.536898+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.437","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cltc has been classified as Amber List (Moderate Evidence).","entity_name":"CLTC","entity_type":"gene"},{"created":"2020-09-03T20:52:51.968363+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-09-03T20:52:51.959733+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-09-03T20:35:33.263340+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Arina Puzriakova","item_type":"entity","text":"reviewed gene: PAK3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31943058; Phenotypes: Intellectual disability; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PAK3","entity_type":"gene"},{"created":"2020-09-03T19:01:28.504024+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STAG1 as ready","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T19:01:28.493424+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stag1 has been classified as Amber List (Moderate Evidence).","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T19:01:19.585132+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.436","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STAG1 were changed from  to Mental retardation, autosomal dominant 47, MIM# 617635","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:59:56.486737+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STAG1 were set to ","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:59:27.198966+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.434","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STAG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:58:58.819997+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: STAG1 as Amber List (moderate evidence)","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:58:58.811396+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stag1 has been classified as Amber List (Moderate Evidence).","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:58:36.122539+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STAG1: Rating: AMBER; Mode of pathogenicity: None; Publications: 28119487; Phenotypes: Mental retardation, autosomal dominant 47, MIM# 617635; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STAG1","entity_type":"gene"},{"created":"2020-09-03T18:54:30.740316+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMC3 as ready","entity_name":"SMC3","entity_type":"gene"},{"created":"2020-09-03T18:54:30.728700+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc3 has been classified as Green List (High Evidence).","entity_name":"SMC3","entity_type":"gene"},{"created":"2020-09-03T18:54:24.868282+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMC3 as Green List (high evidence)","entity_name":"SMC3","entity_type":"gene"},{"created":"2020-09-03T18:54:24.859695+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc3 has been classified as Green List (High Evidence).","entity_name":"SMC3","entity_type":"gene"},{"created":"2020-09-03T18:54:01.064343+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.431","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMC3 was added\ngene: SMC3 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: SMC3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SMC3 were set to Cornelia de Lange syndrome 3, MIM#\t610759\nReview for gene: SMC3 was set to GREEN\nAdded comment: Well established gene-disease association, microcephaly is part of the phenotype. \nSources: Expert list","entity_name":"SMC3","entity_type":"gene"},{"created":"2020-09-03T18:52:19.981651+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMC1A as ready","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-09-03T18:52:19.971683+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc1a has been classified as Green List (High Evidence).","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-09-03T18:52:17.468321+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMC1A as Green List (high evidence)","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-09-03T18:52:17.457965+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc1a has been classified as Green List (High Evidence).","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-09-03T18:51:50.382152+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.429","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMC1A was added\ngene: SMC1A was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: SMC1A was set to Other\nPhenotypes for gene: SMC1A were set to Cornelia de Lange syndrome 2, MIM#\t300590\nReview for gene: SMC1A was set to GREEN\nAdded comment: XLD. Well established gene-disease association. Microcephaly is part of the phenotype. \nSources: Expert list","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-09-03T18:49:23.622510+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.428","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLX4 as ready","entity_name":"SLX4","entity_type":"gene"},{"created":"2020-09-03T18:49:23.609608+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.428","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slx4 has been classified as Green List (High Evidence).","entity_name":"SLX4","entity_type":"gene"},{"created":"2020-09-03T18:49:18.445803+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.428","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLX4 as Green List (high evidence)","entity_name":"SLX4","entity_type":"gene"},{"created":"2020-09-03T18:49:18.434965+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.428","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slx4 has been classified as Green List (High Evidence).","entity_name":"SLX4","entity_type":"gene"},{"created":"2020-09-03T18:48:37.652658+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.427","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLX4 was added\ngene: SLX4 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: SLX4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SLX4 were set to Fanconi anemia, complementation group P, MIM#613951\nReview for gene: SLX4 was set to GREEN\nAdded comment: Established gene-disease association, microcephaly is part of the phenotype. \nSources: Expert list","entity_name":"SLX4","entity_type":"gene"},{"created":"2020-09-03T18:46:31.645454+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.426","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC2A1 as ready","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2020-09-03T18:46:31.631296+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc2a1 has been classified as Green List (High Evidence).","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2020-09-03T18:46:23.413330+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.426","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC2A1 were changed from  to GLUT1 deficiency syndrome 1, infantile onset, severe, MIM# 606777","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2020-09-03T18:45:49.811790+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.425","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC2A1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2020-09-03T18:45:21.934250+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: GLUT1 deficiency syndrome 1, infantile onset, severe, MIM# 606777; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2020-09-03T18:09:59.168555+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC1A4 as ready","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:09:59.154141+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc1a4 has been classified as Green List (High Evidence).","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:09:04.081372+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC1A4 were changed from  to Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:09:02.643442+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC1A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25930971, 26138499, 26041762, 27193218, 29989513; Phenotypes: Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:08:47.649214+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.423","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC1A4 were set to ","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:08:19.913800+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: SLC1A4.","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:08:04.555196+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC1A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:07:39.265811+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC1A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25930971, 26138499, 26041762, 27193218, 29989513; Phenotypes: Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2020-09-03T18:00:46.615534+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RUSC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 27612186; Phenotypes: Mental retardation, autosomal recessive 61, MIM# 617773; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RUSC2","entity_type":"gene"},{"created":"2020-09-03T17:56:30.496713+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL10 as ready","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:56:30.485165+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl10 has been classified as Green List (High Evidence).","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:56:24.157753+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4187","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL10 were changed from  to Mental retardation, X-linked, syndromic, 35, MIM# 300998","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:56:06.452915+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4186","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL10 were set to ","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:55:47.413298+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4185","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL10 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:55:30.687637+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4184","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RPL10: Rating: GREEN; Mode of pathogenicity: None; Publications: 25316788, 25846674, 26290468; Phenotypes: Mental retardation, X-linked, syndromic, 35, MIM# 300998; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:55:18.812763+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL10 as ready","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:55:18.801004+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl10 has been classified as Green List (High Evidence).","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:54:36.025058+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPL10 as Green List (high evidence)","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:54:36.013829+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl10 has been classified as Green List (High Evidence).","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:54:13.694708+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.420","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPL10 was added\ngene: RPL10 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: RPL10 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: RPL10 were set to 25316788; 25846674; 26290468\nPhenotypes for gene: RPL10 were set to Mental retardation, X-linked, syndromic, 35, MIM#\t300998\nReview for gene: RPL10 was set to GREEN\nAdded comment: At least three families reported. Progressive microcephaly, up to -9.6 SD described. \nSources: Expert list","entity_name":"RPL10","entity_type":"gene"},{"created":"2020-09-03T17:50:16.214664+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNU4ATAC as ready","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2020-09-03T17:50:16.206052+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnu4atac has been classified as Green List (High Evidence).","entity_name":"RNU4ATAC","entity_type":"gene"},{"created":"2020-09-03T17:49:40.074560+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNU4ATAC as Green List (high evidence)","entity_name":"RNU4ATAC","entity_type":"gene"}]}