{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=919","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=917","results":[{"created":"2022-03-23T18:13:56.627096+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11836","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NLGN3 were set to ","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:11:49.165070+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11835","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NLGN3 were changed from  to X-linked complex neurodevelopmental disorder MONDO:0100148; {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:11:06.995938+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NLGN3 as ready","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:11:06.985722+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nlgn3 has been classified as Green List (High Evidence).","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:11:04.063746+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NLGN3 were changed from {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425 to X-linked complex neurodevelopmental disorder MONDO:0100148; {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:10:04.033662+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11834","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NLRC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25217959, 25385754, 25217960; Phenotypes: ?Familial cold autoinflammatory syndrome 4 - MIM#616115, Autoinflammation with infantile enterocolitis - MIM#616050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NLRC4","entity_type":"gene"},{"created":"2022-03-23T18:10:00.370538+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.134","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NLRC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25217959, 25385754, 25217960; Phenotypes: ?Familial cold autoinflammatory syndrome 4 - MIM#616115, Autoinflammation with infantile enterocolitis - MIM#616050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NLRC4","entity_type":"gene"},{"created":"2022-03-23T18:09:47.809394+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NLGN3 were changed from  to {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:09:16.584818+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NLGN3 were set to ","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:08:41.492696+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NLGN3 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T18:08:22.128299+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NLGN3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T17:35:45.623674+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11834","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX3-2 as ready","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:35:45.609830+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11834","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx3-2 has been classified as Green List (High Evidence).","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:35:36.668753+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11834","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NKX3-2 were changed from  to Spondylo-megaepiphyseal-metaphyseal dysplasia - MIM#613330","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:35:13.514761+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11833","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NKX3-2 were set to ","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:32:57.435651+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11832","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NKX3-2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:30:50.895338+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX3-2 as ready","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:30:50.883151+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx3-2 has been classified as Green List (High Evidence).","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:30:48.523136+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NKX3-2 were changed from  to Spondylo-megaepiphyseal-metaphyseal dysplasia (MIM#613330)","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:29:57.173746+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NKX3-2 were set to ","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:29:23.345998+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NKX3-2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T17:28:16.880141+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11831","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIPAL4 as ready","entity_name":"NIPAL4","entity_type":"gene"},{"created":"2022-03-23T17:28:16.871102+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11831","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nipal4 has been classified as Green List (High Evidence).","entity_name":"NIPAL4","entity_type":"gene"},{"created":"2022-03-23T17:26:49.160097+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11831","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NIPAL4 were changed from  to Ichthyosis, congenital, autosomal recessive 6 - MIM#612281","entity_name":"NIPAL4","entity_type":"gene"},{"created":"2022-03-23T17:26:29.363531+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11830","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NIPAL4 were set to ","entity_name":"NIPAL4","entity_type":"gene"},{"created":"2022-03-23T17:26:09.556679+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11829","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NIPAL4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIPAL4","entity_type":"gene"},{"created":"2022-03-23T17:17:09.482597+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4589","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NHS as ready","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:17:09.472683+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4589","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhs has been classified as Green List (High Evidence).","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:16:45.372228+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4589","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NHS were changed from  to Nance-Horan syndrome - MIM#302350; Cataract 40, X-linked - MIM#302200","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:14:18.018667+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4588","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NHS were set to ","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:13:43.912647+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4587","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NHS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:12:51.730313+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11828","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NHS as ready","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:12:51.719103+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11828","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhs has been classified as Green List (High Evidence).","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:12:44.182246+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11828","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NHS were changed from  to Nance-Horan syndrome - MIM#302350; Cataract 40, X-linked - MIM#302200","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:12:20.713472+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11827","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NHS were set to ","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:11:57.117704+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11826","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NHS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"NHS","entity_type":"gene"},{"created":"2022-03-23T17:11:11.599851+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11825","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFKBIL1 as ready","entity_name":"NFKBIL1","entity_type":"gene"},{"created":"2022-03-23T17:11:11.590456+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11825","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfkbil1 has been classified as Red List (Low Evidence).","entity_name":"NFKBIL1","entity_type":"gene"},{"created":"2022-03-23T17:11:02.347891+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11825","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFKBIL1 were changed from  to {Rheumatoid arthritis, susceptibility to} - MIM#180300","entity_name":"NFKBIL1","entity_type":"gene"},{"created":"2022-03-23T17:09:35.629751+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11824","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFKBIL1 as Red List (low evidence)","entity_name":"NFKBIL1","entity_type":"gene"},{"created":"2022-03-23T17:09:35.620130+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11824","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfkbil1 has been classified as Red List (Low Evidence).","entity_name":"NFKBIL1","entity_type":"gene"},{"created":"2022-03-23T17:08:42.133419+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFIA as ready","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:08:42.124311+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfia has been classified as Green List (High Evidence).","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:08:39.426167+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.424","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFIA were changed from  to Brain malformations with or without urinary tract defects - MIM#613735","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:08:10.071229+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.423","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NFIA were set to ","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:07:39.971703+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.422","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:06:53.693373+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11823","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFIA as ready","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:06:53.681569+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11823","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfia has been classified as Green List (High Evidence).","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:06:45.317322+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11823","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFIA were changed from  to Brain malformations with or without urinary tract defects - MIM#613735","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:06:00.798181+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11822","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NFIA were set to ","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:05:39.800115+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11821","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFIA was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:03:37.797662+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFIA as Green List (high evidence)","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:03:37.759901+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfia has been classified as Green List (High Evidence).","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:03:36.242044+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11820","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:01:01.743545+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NFIA was added\ngene: NFIA was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic. Sources: Expert Review\nMode of inheritance for gene: NFIA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NFIA were set to 35018717; 33973697; 32926563\nPhenotypes for gene: NFIA were set to Brain malformations with or without urinary tract defects - MIM#613735\nReview for gene: NFIA was set to GREEN\nAdded comment: Haploinsufficiency of the NFIA gene causes NFIA-related disorder, which includes brain abnormalities and intellectual disability, with or without urinary tract defects. \nSources: Expert Review","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T17:00:47.782602+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4586","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NFIA were changed from  to Brain malformations with or without urinary tract defects - MIM#613735","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T16:59:15.557900+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4585","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NFIA were set to ","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T16:58:26.295660+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4584","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFIA was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T16:58:02.175045+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4584","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NFIA","entity_type":"gene"},{"created":"2022-03-23T16:57:04.787043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11819","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:57:04.775033+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11819","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:56:56.803459+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11819","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEXN were changed from  to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:54:06.600691+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11818","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEXN were set to ","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:53:27.597426+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11817","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:53.414002+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:53.402448+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Red List (Low Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:50.478389+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEXN were changed from  to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:21.435638+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.420","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEXN were set to ","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:45.469792+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:16.994774+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.418","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Red List (low evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:16.983706+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.418","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Red List (Low Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:36.713164+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:36.704067+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:00.886021+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Green List (high evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:00.874130+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:49:29.448770+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:49:29.430173+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:48:28.217587+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Green List (high evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:48:28.207055+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:42:03.273703+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:42:03.260274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:41:56.457137+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:41:24.062098+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4582","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:40:49.147959+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4581","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:40:12.963676+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4580","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:54.186283+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:54.172574+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:50.550648+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:05.805595+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1502","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:37:14.340271+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:36:21.043760+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1500","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:58.914387+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: STX1B: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:26.595099+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:26.583406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:17.344578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:34:55.740042+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11815","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:32:28.567712+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11814","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:32:09.403488+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: None","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:28:50.949819+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX2 as ready","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:28:50.938421+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx2 has been classified as Red List (Low Evidence).","entity_name":"STX2","entity_type":"gene"}]}