{"count":220966,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1623","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1621","results":[{"created":"2020-08-31T22:08:37.795164+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: osgep has been classified as Green List (High Evidence).","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:08:08.407829+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4048","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSGEP as ready","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:08:08.397460+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4048","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: osgep has been classified as Green List (High Evidence).","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:08:02.392185+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4048","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSGEP were changed from  to Galloway-Mowat syndrome 3, MIM# 617729","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:07:46.597580+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4047","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSGEP were set to ","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:07:29.382462+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4046","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSGEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:07:14.308256+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4045","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OSGEP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828, 28272532; Phenotypes: Galloway-Mowat syndrome 3, MIM# 617729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:06:25.125466+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSGEP were changed from  to Galloway-Mowat syndrome 3, MIM# 617729","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:05:59.340388+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSGEP were set to ","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:05:24.358878+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.236","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSGEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T22:04:58.104905+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OSGEP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828, 28272532; Phenotypes: Galloway-Mowat syndrome 3, MIM# 617729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSGEP","entity_type":"gene"},{"created":"2020-08-31T21:59:24.659379+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4045","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: NUP107.","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:59:00.634783+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP107 as ready","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:59:00.615717+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup107 has been classified as Green List (High Evidence).","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:58:57.711188+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUP107 were changed from  to Galloway-Mowat syndrome 7, MIM# 618348","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:58:35.797318+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUP107 were set to ","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:58:09.318086+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUP107 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:57:48.832316+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: NUP107.","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:57:39.831879+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NUP107: Rating: GREEN; Mode of pathogenicity: None; Publications: 28280135, 28117080, 30179222, 25558065; Phenotypes: Galloway-Mowat syndrome 7, MIM# 618348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:57:04.853804+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4045","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP107 as ready","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:57:04.843292+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4045","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup107 has been classified as Green List (High Evidence).","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:56:58.864096+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4045","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUP107 were changed from  to Galloway-Mowat syndrome 7, MIM# 618348","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:56:44.382292+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4044","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUP107 were set to ","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:56:29.448895+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4043","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUP107 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:56:12.187730+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4042","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NUP107: Rating: GREEN; Mode of pathogenicity: None; Publications: 28280135, 28117080, 30179222, 25558065; Phenotypes: Galloway-Mowat syndrome 7, MIM# 618348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:55:12.561140+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP107 as ready","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:55:12.552720+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup107 has been classified as Green List (High Evidence).","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:55:08.400517+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: NUP107.","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:55:00.235624+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUP107 were changed from  to Galloway-Mowat syndrome 7, MIM# 618348","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:54:43.367473+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.234","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUP107 were set to ","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:54:06.646555+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUP107 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:53:37.232951+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NUP107: Rating: GREEN; Mode of pathogenicity: None; Publications: 28280135, 28117080, 30179222, 25558065; Phenotypes: Galloway-Mowat syndrome 7, MIM# 618348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUP107","entity_type":"gene"},{"created":"2020-08-31T21:25:02.088682+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VRK1 as ready","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T21:25:02.068922+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vrk1 has been classified as Green List (High Evidence).","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T21:24:16.821936+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VRK1 were changed from  to Pontocerebellar hypoplasia type 1A MIM#607596","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T21:23:57.950214+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.231","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VRK1 were set to ","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T21:23:25.483042+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T21:19:25.534824+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRD4 as ready","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:19:25.526301+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brd4 has been classified as Amber List (Moderate Evidence).","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:19:22.408042+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: BRD4.","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:19:15.056184+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRD4 were changed from  to Cornelia de Lange-like syndrome","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:18:52.553523+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.228","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRD4 were set to ","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:18:25.995534+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.227","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRD4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:18:05.526857+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.226","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BRD4 as Amber List (moderate evidence)","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:18:05.516184+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brd4 has been classified as Amber List (Moderate Evidence).","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T21:16:59.778762+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR4 as ready","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T21:16:59.767909+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr4 has been classified as Green List (High Evidence).","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T21:16:53.914724+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.225","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR4 were changed from  to Galloway-Mowat syndrome 6 MIM#618347","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T21:15:54.069309+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.224","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR4 were set to ","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T21:15:08.837263+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.223","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T19:05:55.729791+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2908","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSD2 as ready","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:05:55.720712+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2908","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsd2 has been classified as Green List (High Evidence).","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:05:50.966486+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2908","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSD2 were set to ","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:05:17.392096+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2907","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSD2 were changed from  to Microcephaly; intellectual disability","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:04:14.288000+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSD2 as ready","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:04:14.279118+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsd2 has been classified as Green List (High Evidence).","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:03:14.489571+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2906","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:02:47.785399+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2905","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30345613, 31171569; Phenotypes: Microcephaly, intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:56.482618+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4042","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSD2 as ready","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:56.472091+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4042","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsd2 has been classified as Green List (High Evidence).","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:49.795901+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4042","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSD2 were changed from  to Microcephaly; intellectual disability","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:34.287969+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4041","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSD2 were set to ","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:17.499338+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4040","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:01:00.724571+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4039","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Microcephaly reported in 6 of 7 individuals with LOF variants in this gene.; to: 7 individuals with LOF variants in this gene, gene thought to be responsible for key features of Wolf-Hirschorn syndrome.","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T19:00:21.420375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4039","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30345613, 31171569; Phenotypes: Microcephaly, intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T18:59:40.383518+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSD2 were changed from  to Microcephaly; intellectual disability","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T18:58:57.280394+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.221","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSD2 were set to ","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T18:58:14.979959+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.220","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T18:57:51.462503+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30345613, 31171569; Phenotypes: Microcephaly, intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD2","entity_type":"gene"},{"created":"2020-08-31T18:54:18.989675+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIPBL as ready","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-08-31T18:54:18.977948+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nipbl has been classified as Green List (High Evidence).","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-08-31T18:54:14.990865+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIPBL as Green List (high evidence)","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-08-31T18:54:14.982596+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nipbl has been classified as Green List (High Evidence).","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-08-31T18:53:58.578358+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.218","user_name":"Paul De Fazio","item_type":"entity","text":"reviewed gene: VRK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19646678, 24126608, 27281532, 31560180; Phenotypes: Pontocerebellar hypoplasia type 1A MIM#607596; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"VRK1","entity_type":"gene"},{"created":"2020-08-31T18:53:45.867525+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.218","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NIPBL was added\ngene: NIPBL was added to Microcephaly. Sources: Expert list\nMode of inheritance for gene: NIPBL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: NIPBL were set to Cornelia de Lange syndrome 1, MIM#\t122470\nReview for gene: NIPBL was set to GREEN\nAdded comment: Well established gene-disease association, microcephaly is a prominent feature of the phenotype. \nSources: Expert list","entity_name":"NIPBL","entity_type":"gene"},{"created":"2020-08-31T18:51:53.168926+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4039","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCAPH as ready","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:51:53.160034+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4039","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncaph has been classified as Red List (Low Evidence).","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:50:59.716329+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4039","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCAPH were changed from  to Microcephaly 23, primary, autosomal recessive 617985","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:50:42.252539+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4038","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCAPH were set to ","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:49:23.724584+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4037","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCAPH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:56.979130+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4036","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NCAPH as Red List (low evidence)","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:56.968034+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4036","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncaph has been classified as Red List (Low Evidence).","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:40.470559+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4035","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NCAPH: Rating: RED; Mode of pathogenicity: None; Publications: 27737959; Phenotypes: Microcephaly 23, primary, autosomal recessive 617985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:08.246538+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.217","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCAPH as ready","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:08.235530+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.217","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncaph has been classified as Red List (Low Evidence).","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:44:05.845296+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.217","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCAPH were changed from  to Microcephaly 23, primary, autosomal recessive 617985","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:43:38.421859+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.216","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCAPH were set to ","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:43:17.186309+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCAPH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:41:23.082086+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NCAPH as Red List (low evidence)","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:41:23.067049+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncaph has been classified as Red List (Low Evidence).","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T18:40:43.225480+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NCAPH: Rating: RED; Mode of pathogenicity: None; Publications: 27737959; Phenotypes: Microcephaly 23, primary, autosomal recessive 617985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCAPH","entity_type":"gene"},{"created":"2020-08-31T17:42:28.219234+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: BRD4: Rating: AMBER; Mode of pathogenicity: None; Publications: 29379197, 30302754; Phenotypes: Cornelia de Lange-like syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"BRD4","entity_type":"gene"},{"created":"2020-08-31T17:40:00.787209+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Paul De Fazio","item_type":"entity","text":"reviewed gene: WDR4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26416026, 28617965, 30079490, 29597095; Phenotypes: Galloway-Mowat syndrome 6 MIM#618347; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-08-31T17:00:44.406488+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCAPD3 as ready","entity_name":"NCAPD3","entity_type":"gene"},{"created":"2020-08-31T17:00:44.392621+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncapd3 has been classified as Amber List (Moderate Evidence).","entity_name":"NCAPD3","entity_type":"gene"},{"created":"2020-08-31T17:00:42.175704+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCAPD3 were changed from  to Microcephaly 22, primary, autosomal recessive, MIM# 617984","entity_name":"NCAPD3","entity_type":"gene"},{"created":"2020-08-31T17:00:24.910857+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCAPD3 were set to 27737959","entity_name":"NCAPD3","entity_type":"gene"},{"created":"2020-08-31T16:59:49.450236+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRCA2 as ready","entity_name":"BRCA2","entity_type":"gene"},{"created":"2020-08-31T16:59:49.438836+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brca2 has been classified as Green List (High Evidence).","entity_name":"BRCA2","entity_type":"gene"},{"created":"2020-08-31T16:59:44.632362+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BRCA2 as Green List (high evidence)","entity_name":"BRCA2","entity_type":"gene"}]}