{"count":220293,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1364","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1362","results":[{"created":"2021-04-02T18:40:41.239636+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BCS1L as ready","entity_name":"BCS1L","entity_type":"gene"},{"created":"2021-04-02T18:40:41.230223+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bcs1l has been classified as Green List (High Evidence).","entity_name":"BCS1L","entity_type":"gene"},{"created":"2021-04-02T18:40:36.254844+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BCS1L were changed from Bjornstad syndrome, GRACILE syndrome, Leigh syndrome, Mitochondrial complex III deficiency, nuclear type 1 to Bjornstad syndrome MIM#262000","entity_name":"BCS1L","entity_type":"gene"},{"created":"2021-04-02T18:40:22.266371+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BCS1L were set to ","entity_name":"BCS1L","entity_type":"gene"},{"created":"2021-04-02T18:01:04.494252+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCM10 as ready","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T18:01:04.483236+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm10 has been classified as Red List (Low Evidence).","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T18:00:57.412427+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MCM10 was added\ngene: MCM10 was added to Cardiomyopathy_Paediatric. Sources: Literature\nMode of inheritance for gene: MCM10 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MCM10 were set to 32865517; 33712616\nPhenotypes for gene: MCM10 were set to Restrictive cardiomyopathy\nReview for gene: MCM10 was set to RED\nAdded comment: PMID 33712616: three affected sibs with restrictive cardiomyopathy and hypoplasia of the spleen and thymus. Functional data suggested that MCM10 deficiency causes chronic replication stress that reduces cell viability due to increased genomic instability and telomere erosion. \nSources: Literature","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T17:59:41.244721+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7000","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCM10 were changed from Susceptibility to CMV to Susceptibility to CMV; Restrictive cardiomyopathy","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T17:59:29.317704+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6999","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCM10 were set to 32865517","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T17:59:07.973033+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6998","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MCM10: Added comment: PMID 33712616: second family reported, three affected sibs with restrictive cardiomyopathy and hypoplasia of the spleen and thymus. Functional data suggested that MCM10 deficiency causes chronic replication stress that reduces cell viability due to increased genomic instability and telomere erosion.; Changed publications: 32865517, 33712616; Changed phenotypes: Susceptibility to CMV, Restrictive cardiomyopathy","entity_name":"MCM10","entity_type":"gene"},{"created":"2021-04-02T17:51:05.951319+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6998","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYBA as ready","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:51:05.940536+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6998","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyba has been classified as Green List (High Evidence).","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:50:58.312725+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6998","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYBA were changed from  to Chronic granulomatous disease 4, autosomal recessive, MIM# 233690; MONDO:0009308","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:50:34.101551+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6997","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYBA were set to ","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:50:17.838067+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6996","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CYBA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:50:00.145187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6995","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CYBA: Rating: GREEN; Mode of pathogenicity: None; Publications: 2770793; Phenotypes: Chronic granulomatous disease 4, autosomal recessive, MIM# 233690, MONDO:0009308; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:49:45.256402+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYBA as ready","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:49:45.245641+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyba has been classified as Green List (High Evidence).","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:49:01.840311+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYBA were set to ","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:48:51.181816+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CYBA: Rating: GREEN; Mode of pathogenicity: None; Publications: 2770793; Phenotypes: Chronic granulomatous disease 4, autosomal recessive, MIM# 233690, MONDO:0009308; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYBA","entity_type":"gene"},{"created":"2021-04-02T17:47:18.421510+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C17orf62 as ready","entity_name":"C17orf62","entity_type":"gene"},{"created":"2021-04-02T17:47:18.411100+11:00","panel_name":"Chronic granulomatous disease","panel_id":3159,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c17orf62 has been classified as Green List (High Evidence).","entity_name":"C17orf62","entity_type":"gene"},{"created":"2021-04-02T17:43:29.798431+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.636","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP37 as ready","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:43:29.788800+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.636","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup37 has been classified as Red List (Low Evidence).","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:43:22.037902+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.636","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NUP37 was added\ngene: NUP37 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: NUP37 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NUP37 were set to 30179222\nPhenotypes for gene: NUP37 were set to Microcephaly 24, primary, autosomal recessive, MIM# 618179\nReview for gene: NUP37 was set to RED\nAdded comment: Single family reported with nephrotic syndrome and microcephaly. \nSources: Expert list","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:42:32.126857+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6995","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUP37 were changed from Nephrotic syndrome to Nephrotic syndrome; Microcephaly 24, primary, autosomal recessive, MIM#\t618179","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:41:53.899647+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6994","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single family reported with nephrotic syndrome. \nSources: Literature; to: Single family reported with nephrotic syndrome and microcephaly.\r\nSources: Literature","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:41:43.488763+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6994","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NUP37: Changed phenotypes: Nephrotic syndrome, Microcephaly 24, primary, autosomal recessive, MIM# 618179","entity_name":"NUP37","entity_type":"gene"},{"created":"2021-04-02T17:38:39.882601+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C7orf43 as ready","entity_name":"C7orf43","entity_type":"gene"},{"created":"2021-04-02T17:38:39.875585+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name TRAPPC14","entity_name":"C7orf43","entity_type":"gene"},{"created":"2021-04-02T17:38:39.852266+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c7orf43 has been classified as Amber List (Moderate Evidence).","entity_name":"C7orf43","entity_type":"gene"},{"created":"2021-04-02T17:38:16.357405+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"C7orf43","entity_type":"gene"},{"created":"2021-04-02T17:38:05.300316+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C7orf43.","entity_name":"C7orf43","entity_type":"gene"},{"created":"2021-04-02T17:36:18.090092+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDFY3 as ready","entity_name":"WDFY3","entity_type":"gene"},{"created":"2021-04-02T17:36:18.080090+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdfy3 has been classified as Green List (High Evidence).","entity_name":"WDFY3","entity_type":"gene"},{"created":"2021-04-02T17:36:11.068127+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WDFY3 as Green List (high evidence)","entity_name":"WDFY3","entity_type":"gene"},{"created":"2021-04-02T17:36:11.059214+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.635","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdfy3 has been classified as Green List (High Evidence).","entity_name":"WDFY3","entity_type":"gene"},{"created":"2021-04-02T17:35:40.651213+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.634","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDFY3 was added\ngene: WDFY3 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: WDFY3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: WDFY3 were set to 31327001; 27008544\nPhenotypes for gene: WDFY3 were set to Microcephaly 18, primary, autosomal dominant, MIM#617520\nReview for gene: WDFY3 was set to GREEN\nAdded comment: >10 individuals with heterozygous variants in this gene and mild/moderate intellectual disability now described in the literature. Some evidence for opposing effects on brain size depending on variant location. \nSources: Expert list","entity_name":"WDFY3","entity_type":"gene"},{"created":"2021-04-02T17:33:18.363965+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6994","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COPB2 as ready","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:33:18.354575+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6994","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: copb2 has been classified as Red List (Low Evidence).","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:33:07.493878+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6994","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COPB2 was added\ngene: COPB2 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: COPB2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COPB2 were set to 29036432\nPhenotypes for gene: COPB2 were set to Microcephaly 19, primary, autosomal recessive, MIM# 617800\nReview for gene: COPB2 was set to RED\nAdded comment: Two sibs with homozygous missense variant in this gene, mice homozygous for this variant had normal brain size however. Mice compound het for null allele and missense variant had some brain features, suggesting the missense variant is hypomorphic. \nSources: Expert list","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:31:41.868108+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.633","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COPB2 as ready","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:31:41.857724+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.633","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: copb2 has been classified as Red List (Low Evidence).","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:31:34.408973+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.633","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: COPB2: Changed rating: RED; Changed phenotypes: Microcephaly 19, primary, autosomal recessive, MIM# 617800","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:31:25.312858+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.633","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COPB2 was added\ngene: COPB2 was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: COPB2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COPB2 were set to 29036432\nPhenotypes for gene: COPB2 were set to Microcephaly 19, primary, autosomal recessive, MIM#\t617800\nReview for gene: COPB2 was set to GREEN\nAdded comment: Two sibs with homozygous missense variant in this gene, mice homozygous for this variant had normal brain size however. Mice compound het for null allele and missense variant had some brain features, suggesting the missense variant is hypomorphic. \nSources: Expert list","entity_name":"COPB2","entity_type":"gene"},{"created":"2021-04-02T17:27:26.061912+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.632","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STIL as ready","entity_name":"STIL","entity_type":"gene"},{"created":"2021-04-02T17:27:26.050708+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.632","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stil has been classified as Green List (High Evidence).","entity_name":"STIL","entity_type":"gene"},{"created":"2021-04-02T17:24:57.763335+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR62 as ready","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:24:57.746265+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr62 has been classified as Green List (High Evidence).","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:24:55.221233+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:24:32.334561+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.276","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:24:09.393858+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.275","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:23:44.212611+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.274","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 20890279, 20729831, 20890278, 21496009, 21834044, 22775483, 32677750, 31788460; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:22:32.351715+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1053","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435 to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:22:12.406922+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1053","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM#604317 to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:21:43.267791+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1052","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WDR62: Changed phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:21:22.324958+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3595","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR62 as ready","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:21:22.315408+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3595","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr62 has been classified as Green List (High Evidence).","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:21:16.369914+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3595","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:20:44.964400+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3594","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:19:46.738345+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3593","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:19:17.648058+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3592","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 20890279, 20729831, 20890278, 21496009, 21834044, 22775483, 32677750, 31788460; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:18:40.966612+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6993","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR62 as ready","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:18:40.956721+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6993","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr62 has been classified as Green List (High Evidence).","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:18:32.305632+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6993","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:17:46.153003+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6992","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:17:27.815351+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6991","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:17:09.940426+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6990","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 20890279, 20729831, 20890278, 21496009, 21834044, 22775483, 32677750, 31788460; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:16:37.107414+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR62 as ready","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:16:37.096333+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr62 has been classified as Green List (High Evidence).","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:16:34.548114+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:16:10.322486+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:15:33.550659+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:15:04.524678+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 20890279, 20729831, 20890278, 21496009, 21834044, 22775483, 32677750, 31788460; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:14:43.386564+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.632","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR62 as ready","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:14:43.376543+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.632","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr62 has been classified as Green List (High Evidence).","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:14:22.346372+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.632","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR62 were changed from  to Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:13:57.220179+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.631","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR62 were set to ","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:13:28.097294+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.630","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR62 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:13:03.093756+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.629","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WDR62: Changed phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317, MONDO:0011435","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:12:38.416818+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.629","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR62: Rating: GREEN; Mode of pathogenicity: None; Publications: 20890279, 20729831, 20890278, 21496009, 21834044, 22775483, 32677750, 31788460; Phenotypes: Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-04-02T17:09:27.208247+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3592","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT10A as ready","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:09:27.198137+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3592","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt10a has been classified as Green List (High Evidence).","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:09:20.220656+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3592","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT10A were changed from  to Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; MONDO:0000208","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:08:56.695746+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3591","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT10A were set to ","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:08:23.896952+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3590","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMT10A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:07:22.398423+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3589","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRMT10A: Rating: GREEN; Mode of pathogenicity: None; Publications: 24204302, 25053765, 33448213, 33067246, 26535115, 26526202, 26297882; Phenotypes: Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033, MONDO:0000208; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:06:30.973034+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6990","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT10A as ready","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:06:30.963977+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6990","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt10a has been classified as Green List (High Evidence).","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:06:12.839044+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6990","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT10A were changed from  to Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; MONDO:0000208","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:05:55.831321+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6989","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT10A were set to ","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:05:29.378445+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6988","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMT10A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:04:25.603797+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6987","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRMT10A: Rating: GREEN; Mode of pathogenicity: None; Publications: 24204302, 25053765, 33448213, 33067246, 26535115, 26526202, 26297882; Phenotypes: Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033, MONDO:0000208; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:03:24.516865+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.629","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT10A as ready","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:03:24.506415+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.629","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt10a has been classified as Green List (High Evidence).","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:03:22.199926+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.629","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT10A were changed from  to Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; MONDO:0000208","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:02:59.313704+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.628","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT10A were set to ","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:02:28.122201+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.627","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMT10A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:01:55.487348+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.626","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TRMT10A: Changed phenotypes: Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033, MONDO:0000208","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2021-04-02T17:01:12.314868+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.626","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRMT10A: Rating: GREEN; Mode of pathogenicity: None; Publications: 24204302, 25053765, 33448213, 33067246, 26535115, 26526202, 26297882; Phenotypes: Microcephaly, short stature, and impaired glucose metabolism 1, MIM# 616033; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMT10A","entity_type":"gene"}]}