{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2083","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2081","results":[{"created":"2019-11-28T16:46:16.517575+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGFR3 as Green List (high evidence)","entity_name":"FGFR3","entity_type":"gene"},{"created":"2019-11-28T16:46:16.510075+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2019-11-28T16:45:39.784842+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGFR3 was added\ngene: FGFR3 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: FGFR3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FGFR3 were set to LADD syndrome, MIM#149730\nReview for gene: FGFR3 was set to GREEN\nAdded comment: CAKUT is a feature of LADD syndrome. \nSources: Expert list","entity_name":"FGFR3","entity_type":"gene"},{"created":"2019-11-28T16:29:03.944081+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DACT1 as ready","entity_name":"DACT1","entity_type":"gene"},{"created":"2019-11-28T16:29:03.935744+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dact1 has been classified as Amber List (Moderate Evidence).","entity_name":"DACT1","entity_type":"gene"},{"created":"2019-11-28T16:28:54.760255+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DACT1 as Amber List (moderate evidence)","entity_name":"DACT1","entity_type":"gene"},{"created":"2019-11-28T16:28:54.753223+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dact1 has been classified as Amber List (Moderate Evidence).","entity_name":"DACT1","entity_type":"gene"},{"created":"2019-11-28T16:28:25.214310+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DACT1 was added\ngene: DACT1 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: DACT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DACT1 were set to 28054444\nPhenotypes for gene: DACT1 were set to Townes-Brocks syndrome 2, MIM#617466\nReview for gene: DACT1 was set to AMBER\nAdded comment: Single multigenerational family with a heterozygous variant in this gene and features of TBS including CAKUT. \nSources: Expert list","entity_name":"DACT1","entity_type":"gene"},{"created":"2019-11-28T16:21:37.753007+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COQ7 as ready","entity_name":"COQ7","entity_type":"gene"},{"created":"2019-11-28T16:21:37.745418+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq7 has been classified as Green List (High Evidence).","entity_name":"COQ7","entity_type":"gene"},{"created":"2019-11-28T16:21:33.292882+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ7 as Green List (high evidence)","entity_name":"COQ7","entity_type":"gene"},{"created":"2019-11-28T16:21:33.284949+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq7 has been classified as Green List (High Evidence).","entity_name":"COQ7","entity_type":"gene"},{"created":"2019-11-28T16:21:05.090879+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COQ7 was added\ngene: COQ7 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: COQ7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COQ7 were set to 31240163; 28409910; 26084283\nPhenotypes for gene: COQ7 were set to Coenzyme Q10 deficiency, primary, 8, MIM#616733\nReview for gene: COQ7 was set to GREEN\nAdded comment: Three individuals described in the literature, renal disease prominent in at least two. \nSources: Expert list","entity_name":"COQ7","entity_type":"gene"},{"created":"2019-11-28T16:13:58.377725+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CENPF as ready","entity_name":"CENPF","entity_type":"gene"},{"created":"2019-11-28T16:13:58.370799+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cenpf has been classified as Green List (High Evidence).","entity_name":"CENPF","entity_type":"gene"},{"created":"2019-11-28T16:13:53.981945+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CENPF as Green List (high evidence)","entity_name":"CENPF","entity_type":"gene"},{"created":"2019-11-28T16:13:53.973411+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cenpf has been classified as Green List (High Evidence).","entity_name":"CENPF","entity_type":"gene"},{"created":"2019-11-28T16:13:27.102981+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CENPF was added\ngene: CENPF was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: CENPF was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CENPF were set to Stromme syndrome, MIM#243605\nReview for gene: CENPF was set to GREEN\nAdded comment: CAKUT is part of the phenotype. \nSources: Expert list","entity_name":"CENPF","entity_type":"gene"},{"created":"2019-11-28T14:19:51.437658+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EZH2 as ready","entity_name":"EZH2","entity_type":"gene"},{"created":"2019-11-28T14:19:51.429870+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ezh2 has been classified as Red List (Low Evidence).","entity_name":"EZH2","entity_type":"gene"},{"created":"2019-11-28T14:19:48.402376+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EZH2 as Red List (low evidence)","entity_name":"EZH2","entity_type":"gene"},{"created":"2019-11-28T14:19:48.394206+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ezh2 has been classified as Red List (Low Evidence).","entity_name":"EZH2","entity_type":"gene"},{"created":"2019-11-28T14:19:16.105223+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXC1 as ready","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-28T14:19:16.097653+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxc1 has been classified as Red List (Low Evidence).","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-28T14:19:08.488987+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXC1 as Red List (low evidence)","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-28T14:19:08.480906+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxc1 has been classified as Red List (Low Evidence).","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-28T14:18:31.423745+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEMA3A as ready","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:18:31.416603+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3a has been classified as Red List (Low Evidence).","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:18:26.831016+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3A as Red List (low evidence)","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:18:26.821003+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3a has been classified as Red List (Low Evidence).","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:18:10.426745+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3A as Red List (low evidence)","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:18:10.406595+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3a has been classified as Red List (Low Evidence).","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:17:53.336596+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3A as Red List (low evidence)","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:17:53.318651+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3a has been classified as Red List (Low Evidence).","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:17:36.944872+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3A as Red List (low evidence)","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T14:17:36.859202+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3a has been classified as Red List (Low Evidence).","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T13:48:23.421139+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ABCC6 as ready","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:48:23.417946+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"entity","text":"Added comment: Comment when marking as ready: Agree not an ID gene","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:48:23.377007+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"entity","text":"Gene: abcc6 has been classified as Red List (Low Evidence).","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:47:44.395668+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: ABCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:47:10.299001+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.17","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: ABCC6 as Red List (low evidence)","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:47:10.288253+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.17","user_name":"Chirag Patel","item_type":"entity","text":"Gene: abcc6 has been classified as Red List (Low Evidence).","entity_name":"ABCC6","entity_type":"gene"},{"created":"2019-11-28T13:45:27.990469+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHD3 as ready","entity_name":"CHD3","entity_type":"gene"},{"created":"2019-11-28T13:45:27.983379+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd3 has been classified as Green List (High Evidence).","entity_name":"CHD3","entity_type":"gene"},{"created":"2019-11-28T13:45:19.766476+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHD3 as Green List (high evidence)","entity_name":"CHD3","entity_type":"gene"},{"created":"2019-11-28T13:45:19.758032+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd3 has been classified as Green List (High Evidence).","entity_name":"CHD3","entity_type":"gene"},{"created":"2019-11-28T13:43:40.576656+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ABAT as ready","entity_name":"ABAT","entity_type":"gene"},{"created":"2019-11-28T13:43:40.568537+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: abat has been classified as Green List (High Evidence).","entity_name":"ABAT","entity_type":"gene"},{"created":"2019-11-28T13:43:36.662538+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ABAT were changed from  to GABA-transaminase deficiency, MIM#613163","entity_name":"ABAT","entity_type":"gene"},{"created":"2019-11-28T13:43:19.786860+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ABAT were set to ","entity_name":"ABAT","entity_type":"gene"},{"created":"2019-11-28T13:43:03.085822+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ABAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ABAT","entity_type":"gene"},{"created":"2019-11-28T13:41:59.549021+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AAAS as ready","entity_name":"AAAS","entity_type":"gene"},{"created":"2019-11-28T13:41:59.538448+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aaas has been classified as Green List (High Evidence).","entity_name":"AAAS","entity_type":"gene"},{"created":"2019-11-28T13:41:55.842540+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AAAS were changed from  to Achalasia-addisonianism-alacrimia syndrome, MIM#231550","entity_name":"AAAS","entity_type":"gene"},{"created":"2019-11-28T13:41:37.179014+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AAAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AAAS","entity_type":"gene"},{"created":"2019-11-28T13:37:20.130955+11:00","panel_name":"Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS","panel_id":190,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Renal hypertension and disorders of aldosterone metabolism_KidGen to Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-28T13:24:55.240800+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.8","user_name":"San Lin","item_type":"panel","text":"removed gene:DNAJB11 from the panel","entity_name":null,"entity_type":null},{"created":"2019-11-28T13:24:44.514297+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.7","user_name":"San Lin","item_type":"panel","text":"removed gene:DZIP1L from the panel","entity_name":null,"entity_type":null},{"created":"2019-11-28T13:11:12.354067+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AHI1 as ready","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T13:11:12.346658+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahi1 has been classified as Green List (High Evidence).","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T13:11:08.201118+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AHI1 were changed from Joubert syndrome 3 to Joubert syndrome 3, MIM#608629","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T13:10:31.088950+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AHI1 as Green List (high evidence)","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T13:10:31.080530+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahi1 has been classified as Green List (High Evidence).","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T10:40:58.747329+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.0","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SEMA3A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2019-11-28T10:40:25.209514+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.0","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FOXC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"FOXC1","entity_type":"gene"},{"created":"2019-11-28T10:39:46.146052+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS","panel_id":63,"panel_version":"0.0","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: EZH2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"EZH2","entity_type":"gene"},{"created":"2019-11-28T10:24:56.907404+11:00","panel_name":"Renal amyloidosis_KidGen_VCGS","panel_id":191,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Amyloidosis_KidGen_VCGS to Renal amyloidosis_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-28T10:23:19.946482+11:00","panel_name":"Amyloidosis_KidGen_VCGS","panel_id":191,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Amyloidosis_KidGen to Amyloidosis_KidGen_VCGS","entity_name":null,"entity_type":null},{"created":"2019-11-28T10:22:08.933298+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NLRP3 as ready","entity_name":"NLRP3","entity_type":"gene"},{"created":"2019-11-28T10:22:08.925993+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nlrp3 has been classified as Green List (High Evidence).","entity_name":"NLRP3","entity_type":"gene"},{"created":"2019-11-28T10:22:05.823305+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NLRP3 were changed from Muckle-Wells syndrome to Muckle-Wells syndrome, MIM#191900","entity_name":"NLRP3","entity_type":"gene"},{"created":"2019-11-28T10:21:51.142354+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NLRP3 as Green List (high evidence)","entity_name":"NLRP3","entity_type":"gene"},{"created":"2019-11-28T10:21:51.134968+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nlrp3 has been classified as Green List (High Evidence).","entity_name":"NLRP3","entity_type":"gene"},{"created":"2019-11-28T10:20:58.638809+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LYZ as ready","entity_name":"LYZ","entity_type":"gene"},{"created":"2019-11-28T10:20:58.630948+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyz has been classified as Green List (High Evidence).","entity_name":"LYZ","entity_type":"gene"},{"created":"2019-11-28T10:20:55.507048+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LYZ were changed from Amyloidosis, renal to Amyloidosis, renal, MIM#105200","entity_name":"LYZ","entity_type":"gene"},{"created":"2019-11-28T10:20:44.326347+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LYZ as Green List (high evidence)","entity_name":"LYZ","entity_type":"gene"},{"created":"2019-11-28T10:20:44.319107+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyz has been classified as Green List (High Evidence).","entity_name":"LYZ","entity_type":"gene"},{"created":"2019-11-28T10:20:15.237473+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GSN as ready","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:20:15.230077+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gsn has been classified as Green List (High Evidence).","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:20:11.442613+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GSN were changed from Amyloidosis, Finnish type to Amyloidosis, Finnish type, MIM#105200","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:19:58.584250+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GSN as Green List (high evidence)","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:19:58.576427+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gsn has been classified as Green List (High Evidence).","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:19:16.068555+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGA as ready","entity_name":"FGA","entity_type":"gene"},{"created":"2019-11-28T10:19:16.061339+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fga has been classified as Green List (High Evidence).","entity_name":"FGA","entity_type":"gene"},{"created":"2019-11-28T10:19:13.165582+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGA were changed from Amyloidosis, familial visceral to Amyloidosis, familial visceral, MIM#105200","entity_name":"FGA","entity_type":"gene"},{"created":"2019-11-28T10:18:56.440149+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGA as Green List (high evidence)","entity_name":"FGA","entity_type":"gene"},{"created":"2019-11-28T10:18:56.432501+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fga has been classified as Green List (High Evidence).","entity_name":"FGA","entity_type":"gene"},{"created":"2019-11-28T10:18:12.768317+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: APOA1 as ready","entity_name":"APOA1","entity_type":"gene"},{"created":"2019-11-28T10:18:12.760334+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: apoa1 has been classified as Green List (High Evidence).","entity_name":"APOA1","entity_type":"gene"},{"created":"2019-11-28T10:18:09.909169+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: APOA1 were changed from Amyloidosis, 3 or more types to Amyloidosis, 3 or more types, MIM#105200","entity_name":"APOA1","entity_type":"gene"},{"created":"2019-11-28T10:17:55.630231+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: APOA1 as Green List (high evidence)","entity_name":"APOA1","entity_type":"gene"},{"created":"2019-11-28T10:17:55.622762+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: apoa1 has been classified as Green List (High Evidence).","entity_name":"APOA1","entity_type":"gene"},{"created":"2019-11-28T10:17:44.256519+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.3","user_name":"Chirag Patel","item_type":"entity","text":"gene: FAN1 was added\ngene: FAN1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert list\nMode of inheritance for gene: FAN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FAN1 were set to PubMed: 22772369; 16678356; 7847351; 8546134\nPhenotypes for gene: FAN1 were set to Interstitial nephritis, karyomegalic\nReview for gene: FAN1 was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"FAN1","entity_type":"gene"},{"created":"2019-11-28T10:15:06.798151+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.1","user_name":"Chirag Patel","item_type":"entity","text":"gene: AHI1 was added\ngene: AHI1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert list\nMode of inheritance for gene: AHI1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AHI1 were set to PubMed: 15322546; 15467982; 16453322; 29146704\nPhenotypes for gene: AHI1 were set to Joubert syndrome 3\nReview for gene: AHI1 was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-11-28T10:12:57.259849+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.0","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: DZIP1L: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DZIP1L","entity_type":"gene"},{"created":"2019-11-28T10:12:43.249631+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen","panel_id":193,"panel_version":"0.0","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: DNAJB11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DNAJB11","entity_type":"gene"},{"created":"2019-11-28T10:01:04.413294+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene GSN were changed from PubMed: 8395367; 2176164; 8684801; 6975851; 29167514 to PubMed: 8395367; 2176164; 8684801; 6975851; 29167514","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T10:00:55.659360+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: GSN: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 8395367, 2176164, 8684801, 6975851, 29167514; Phenotypes: Amyloidosis, Finnish type; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GSN","entity_type":"gene"},{"created":"2019-11-28T09:59:58.875578+11:00","panel_name":"Amyloidosis_KidGen","panel_id":191,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"entity","text":"Source KidGen_Amyloidosis v38.1.0 was removed from GSN.\nSource Expert list was added to GSN.\nMode of inheritance for gene GSN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GSN were changed from  to Amyloidosis, Finnish type\nPublications for gene GSN were changed from PubMed: 8395367; 2176164; 8684801; 6975851 to PubMed: 8395367; 2176164; 8684801; 6975851","entity_name":"GSN","entity_type":"gene"}]}