{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=916","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=914","results":[{"created":"2022-03-25T14:00:58.031659+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11912","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:00:22.293464+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMB2 as ready","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T14:00:22.281687+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamb2 has been classified as Green List (High Evidence).","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T14:00:17.850626+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMB2 were changed from  to Pierson syndrome, MIM# 609049; Nephrotic syndrome, type 5, with or without ocular abnormalities, MIM# 614199","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T13:59:45.948298+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMB2 were set to ","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T13:59:12.279020+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T13:58:38.914363+11:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 14136829, 15372515, 17256789; Phenotypes: Pierson syndrome, MIM# 609049, Nephrotic syndrome, type 5, with or without ocular abnormalities, MIM# 614199; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T11:54:39.244803+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11911","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LBR were changed from  to Greenberg skeletal dysplasia, MIM# 215140","entity_name":"LBR","entity_type":"gene"},{"created":"2022-03-25T11:54:37.741830+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11910","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LBR as ready","entity_name":"LBR","entity_type":"gene"},{"created":"2022-03-25T11:54:37.732406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11910","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lbr has been classified as Green List (High Evidence).","entity_name":"LBR","entity_type":"gene"},{"created":"2022-03-25T11:53:48.271369+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11910","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LBR were set to ","entity_name":"LBR","entity_type":"gene"},{"created":"2022-03-25T11:52:51.483318+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11909","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LBR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LBR","entity_type":"gene"},{"created":"2022-03-25T11:42:54.436108+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11908","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LAT as ready","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T11:42:54.425074+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11908","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lat has been classified as Green List (High Evidence).","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T11:41:30.238396+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11908","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T10:59:55.907517+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11907","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LAT were changed from  to Immunodeficiency 52, MIM# 617514","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T10:59:09.314926+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11906","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: LAT: Rating: GREEN; Mode of pathogenicity: None; Publications: 27522155, 27242165, 10204488; Phenotypes: Immunodeficiency 52, MIM# 617514; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T10:54:02.633776+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.232","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: EPHB4: Rating: GREEN; Mode of pathogenicity: None; Publications: 27400125, 35178555; Phenotypes: Lymphatic malformation 7 (MIM#617300), AD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T10:49:18.798267+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11906","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMB2 were changed from  to Pierson syndrome, MIM# 609049; Nephrotic syndrome, type 5, with or without ocular abnormalities, MIM# 614199","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T10:46:51.146347+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11905","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMB2 were set to ","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T10:46:30.625446+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11904","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMB2","entity_type":"gene"},{"created":"2022-03-25T10:45:46.111513+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMPD1 as ready","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:45:46.097354+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smpd1 has been classified as Green List (High Evidence).","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:45:40.959544+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMPD1 were changed from  to Niemann-Pick disease, type A, MIM# 257200; MONDO:0009756","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:45:11.498175+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.231","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMPD1 were set to ","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:44:36.347043+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: L1CAM as ready","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:44:36.333412+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: l1cam has been classified as Green List (High Evidence).","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:44:33.340950+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: L1CAM were changed from  to Hydrocephalus due to aqueductal stenosis, MIM# 307000; MASA syndrome, MIM# 303350; L1 syndrome, MONDO:0017140","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:41:58.800374+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMPD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:41:29.019527+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27928775; Phenotypes: Niemann-Pick disease, type A, MIM# 257200, MONDO:0009756; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMPD1","entity_type":"gene"},{"created":"2022-03-25T10:39:02.657611+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11903","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: L1CAM were changed from Hydrocephalus due to aqueductal stenosis, MIM# 307000; MASA syndrome, MIM# 303350; L1 syndrome, MONDO:0017140 to Hydrocephalus due to aqueductal stenosis, MIM# 307000; MASA syndrome, MIM# 303350; L1 syndrome, MONDO:0017140; Corpus callosum, partial agenesis of, MIM# 304100","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:38:30.239417+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11902","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: L1CAM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hydrocephalus due to aqueductal stenosis, MIM# 307000, Corpus callosum, partial agenesis of, MIM# 304100; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:35:26.597449+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: L1CAM were set to ","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:34:58.895709+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: L1CAM was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:34:26.119186+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: L1CAM: Rating: GREEN; Mode of pathogenicity: None; Publications: 11438988, 7920660, 8401593, 19565280; Phenotypes: Hydrocephalus due to aqueductal stenosis, MIM# 307000, MASA syndrome, MIM# 303350, L1 syndrome, MONDO:0017140; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:30:34.545674+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11902","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: L1CAM were set to ","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:30:13.098851+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11901","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: L1CAM was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"L1CAM","entity_type":"gene"},{"created":"2022-03-25T10:29:24.099039+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1507","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPRL3 as ready","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:29:24.086792+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1507","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nprl3 has been classified as Green List (High Evidence).","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:29:21.009838+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1507","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPRL3 were changed from  to Epilepsy, familial focal, with variable foci 3- MIM#617118","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:28:44.800351+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPRL3 were set to ","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:28:07.781133+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1505","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPRL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:27:17.088376+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11900","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPRL3 as ready","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:27:17.077548+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11900","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nprl3 has been classified as Green List (High Evidence).","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:27:09.383176+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11900","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPRL3 were changed from  to Epilepsy, familial focal, with variable foci 3- MIM#617118","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:26:41.613015+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11899","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPRL3 were set to ","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T10:23:21.352230+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: GUSB: Rating: GREEN; Mode of pathogenicity: None; Publications: 30442200; Phenotypes: Mucopolysaccharidosis VII, MIM# 253220, MONDO:0009662; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T10:15:50.587198+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11898","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPRL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NPRL3","entity_type":"gene"},{"created":"2022-03-25T09:15:18.802776+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11897","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPPC as ready","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:15:18.787507+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11897","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nppc has been classified as Red List (Low Evidence).","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:08:28.231630+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11897","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPPC were changed from  to short stature and non-specific skeletal anomalies - MONDO#0014551","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:08:08.862381+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11896","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPPC were set to ","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:07:47.834588+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11895","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPPC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:07:29.489432+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11894","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPPC as Red List (low evidence)","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:07:29.479239+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11894","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nppc has been classified as Red List (Low Evidence).","entity_name":"NPPC","entity_type":"gene"},{"created":"2022-03-25T09:06:29.283971+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH2 as ready","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:06:29.272000+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch2 has been classified as Green List (High Evidence).","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:06:26.849451+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from  to Alagille syndrome 2 (MIM#610205)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:05:58.632597+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.224","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH2 were set to ","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:05:29.073426+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.223","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:04:45.512676+11:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NOTCH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Alagille syndrome 2 (MIM#610205); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:04:31.644162+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from Alagille syndrome 2 (MIM#610205); Hajdu-Cheney syndrome (MIM#102500) to Hajdu-Cheney syndrome (MIM#102500)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:03:28.007062+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH2 as ready","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:03:27.992926+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch2 has been classified as Green List (High Evidence).","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:03:25.505569+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from  to Alagille syndrome 2 (MIM#610205); Hajdu-Cheney syndrome (MIM#102500)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:01:49.047488+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH2 were set to ","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:01:20.105247+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:00:22.390606+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH2 as ready","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:00:22.377574+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch2 has been classified as Green List (High Evidence).","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T09:00:19.202574+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from  to Alagille syndrome 2 (MIM#610205); Hajdu-Cheney syndrome (MIM#102500)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:58:31.598743+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH2 were set to ","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:57:58.630643+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.204","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:57:07.520295+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH2 as ready","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:57:07.508188+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch2 has been classified as Green List (High Evidence).","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:56:52.475518+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from  to Alagille syndrome 2 (MIM#610205); Hajdu-Cheney syndrome (MIM#102500)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:56:21.478361+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH2 were set to ","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:55:51.745897+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:54:59.437516+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11893","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH2 as ready","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:54:59.425384+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11893","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch2 has been classified as Green List (High Evidence).","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:54:13.174206+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11893","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH2 were changed from  to Alagille syndrome 2 (MIM#610205); Hajdu-Cheney syndrome (MIM#102500)","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:53:52.740220+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11892","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH2 were set to ","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:53:33.451834+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11891","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH2","entity_type":"gene"},{"created":"2022-03-25T08:52:44.104361+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11890","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH1 as ready","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:52:44.094799+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11890","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch1 has been classified as Green List (High Evidence).","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:49:57.624614+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11890","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH1 were changed from  to Adams-Oliver syndrome 5 (MIM#616028)","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:49:37.539196+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11889","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH1 were set to ","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:48:14.353372+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11888","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:47:25.450459+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.203","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOTCH1 as ready","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:47:25.437006+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.203","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: notch1 has been classified as Green List (High Evidence).","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:47:22.701192+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.203","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOTCH1 were changed from  to Adams-Oliver syndrome 5 (MIM#616028)","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:46:52.961396+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOTCH1 were set to ","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:42:54.813755+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOTCH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NOTCH1","entity_type":"gene"},{"created":"2022-03-25T08:42:10.928705+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11887","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NONO as ready","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:42:10.906666+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11887","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nono has been classified as Green List (High Evidence).","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:42:02.375095+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11887","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NONO were changed from  to Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:41:35.203842+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11886","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NONO were set to ","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:41:13.885430+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11885","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NONO was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:40:41.224051+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4601","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NONO as ready","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:40:41.207614+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4601","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nono has been classified as Green List (High Evidence).","entity_name":"NONO","entity_type":"gene"},{"created":"2022-03-25T08:40:37.175074+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4601","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NONO were changed from  to Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967","entity_name":"NONO","entity_type":"gene"}]}