{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1795","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1793","results":[{"created":"2020-05-21T12:51:02.418582+10:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ABCB6 was added\ngene: ABCB6 was added to Anophthalmia_Microphthalmia_Coloboma. Sources: Literature\nMode of inheritance for gene: ABCB6 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ABCB6 were set to 22226084; 24281366\nPhenotypes for gene: ABCB6 were set to Microphthalmia, isolated, with coloboma 7 MIM#614497\nReview for gene: ABCB6 was set to RED\nAdded comment: Segregation of a missense variant reported in a single Chinese family. Morpholino knockdown of abcb6 in zebrafish produces a phenotype characteristic of coloboma. The missenses p.Ala57Thr and p.Arg192Gln reported in cases with coloboma are too common in gnomAD for a dominant condition. No convincing evidence reported since the 2012 publication. \nSources: Literature","entity_name":"ABCB6","entity_type":"gene"},{"created":"2020-05-21T12:50:08.694941+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B9D1 as Amber List (moderate evidence)","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:50:08.686343+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d1 has been classified as Amber List (Moderate Evidence).","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:43:49.513731+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B9D1: Rating: AMBER; Mode of pathogenicity: None; Publications: 24886560, 21493627, 25920555; Phenotypes: Meckel syndrome 9, MIM# 614209, Joubert syndrome 27, MIM# 617120; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:40:55.444982+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B9D1 as ready","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:40:55.431306+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d1 has been classified as Amber List (Moderate Evidence).","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:40:52.704703+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B9D1 were changed from  to Meckel syndrome 9, MIM# 614209; Joubert syndrome 27, MIM# 617120","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:40:13.413033+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.178","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B9D1 were set to ","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:39:44.807657+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.177","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B9D1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:39:17.174953+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B9D1 as Amber List (moderate evidence)","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:39:17.164676+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.176","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d1 has been classified as Amber List (Moderate Evidence).","entity_name":"B9D1","entity_type":"gene"},{"created":"2020-05-21T12:17:55.904689+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.57","user_name":"Lauren Akesson","item_type":"entity","text":"reviewed gene: L1CAM: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 9926316, 27066571; Phenotypes: L1CAM-related disease; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"L1CAM","entity_type":"gene"},{"created":"2020-05-21T12:11:19.042517+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOPORS as ready","entity_name":"TOPORS","entity_type":"gene"},{"created":"2020-05-21T12:11:19.029602+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: topors has been classified as Green List (High Evidence).","entity_name":"TOPORS","entity_type":"gene"},{"created":"2020-05-21T12:11:07.242009+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOPORS as Green List (high evidence)","entity_name":"TOPORS","entity_type":"gene"},{"created":"2020-05-21T12:11:07.232861+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: topors has been classified as Green List (High Evidence).","entity_name":"TOPORS","entity_type":"gene"},{"created":"2020-05-21T12:08:15.921906+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBIP1: Changed publications: 24026985, 32055034","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:03:32.963568+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to 24026985","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:02:50.781402+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBIP1: Added comment: Additional family reported.; Changed publications: 24026985, 32055034V","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:02:18.121721+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2842","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBIP1 were changed from  to Bardet-Biedl syndrome 18, MIM#615995","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:01:58.418634+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2841","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to ","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:01:38.403594+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2840","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:01:17.086807+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2839","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: BBIP1: Added comment: Additional family reported.; Changed publications: 24026985, 32055034","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T12:00:16.127752+10:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to 24026985","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T11:59:15.165451+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to 24026985","entity_name":"BBIP1","entity_type":"gene"},{"created":"2020-05-21T11:52:02.589833+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.57","user_name":"Lauren Akesson","item_type":"entity","text":"reviewed gene: GRIN2B: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 28377535; Phenotypes: GRIN2B-related neurodevelopmental disorder; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GRIN2B","entity_type":"gene"},{"created":"2020-05-21T11:31:56.822417+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.18","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: ABCB11: Rating: GREEN; Mode of pathogenicity: None; Publications: 23141890; Phenotypes: Cholestasis, benign recurrent intrahepatic, 2 605479 AR, Cholestasis, progressive familial intrahepatic 2 601847 AR; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"ABCB11","entity_type":"gene"},{"created":"2020-05-21T11:29:55.302169+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.57","user_name":"Lauren Akesson","item_type":"entity","text":"reviewed gene: GRIN1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 29365063; Phenotypes: GRIN1-related neurodevelopmental disorder; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GRIN1","entity_type":"gene"},{"created":"2020-05-21T09:00:08.628465+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TULP1 as ready","entity_name":"TULP1","entity_type":"gene"},{"created":"2020-05-21T09:00:08.618538+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tulp1 has been classified as Green List (High Evidence).","entity_name":"TULP1","entity_type":"gene"},{"created":"2020-05-21T09:00:03.158451+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TULP1 as Green List (high evidence)","entity_name":"TULP1","entity_type":"gene"},{"created":"2020-05-21T09:00:03.146430+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tulp1 has been classified as Green List (High Evidence).","entity_name":"TULP1","entity_type":"gene"},{"created":"2020-05-20T21:47:36.234177+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Amber List (moderate evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:47:36.223436+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Amber List (Moderate Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:47:04.797707+10:00","panel_name":"Renal Ciliopathies and Nephronophthisis","panel_id":193,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ZNF423: Changed rating: AMBER","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:46:21.717953+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2839","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Amber List (moderate evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:46:21.705740+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2839","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Amber List (Moderate Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:46:00.117309+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2838","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ZNF423: Changed rating: AMBER","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:45:19.527961+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF423 as ready","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:45:19.514941+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Amber List (Moderate Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:45:14.511839+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Amber List (moderate evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:45:14.497207+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Amber List (Moderate Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:43:29.438907+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF423 as Amber List (moderate evidence)","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:43:29.426525+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf423 has been classified as Amber List (Moderate Evidence).","entity_name":"ZNF423","entity_type":"gene"},{"created":"2020-05-20T21:09:39.904475+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPD1L as ready","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:09:39.896048+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpd1l has been classified as Amber List (Moderate Evidence).","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:09:37.143866+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPD1L were changed from  to Brugada syndrome 2, MIM# 611777","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:09:13.704022+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPD1L were set to ","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:08:49.726416+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GPD1L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:08:22.878166+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GPD1L as Amber List (moderate evidence)","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:08:22.866011+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpd1l has been classified as Amber List (Moderate Evidence).","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:07:56.515238+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: GPD1L.","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:07:48.099790+10:00","panel_name":"Incidentalome","panel_id":126,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GPD1L: Rating: AMBER; Mode of pathogenicity: None; Publications: 17967977, 19666841; Phenotypes: Brugada syndrome 2, MIM# 611777; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:06:44.753923+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPD1L as ready","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:06:44.749734+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Rated as DISPUTED by ClinGen.","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:06:44.718188+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpd1l has been classified as Amber List (Moderate Evidence).","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:06:35.701372+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPD1L were changed from  to Brugada syndrome 2, MIM# 611777","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:06:10.983133+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPD1L were set to ","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:05:37.840680+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GPD1L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:05:12.503276+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: GPD1L.","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:04:53.409234+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GPD1L as Amber List (moderate evidence)","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:04:53.393194+10:00","panel_name":"Brugada syndrome","panel_id":60,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpd1l has been classified as Amber List (Moderate Evidence).","entity_name":"GPD1L","entity_type":"gene"},{"created":"2020-05-20T21:03:55.816364+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POC1B as ready","entity_name":"POC1B","entity_type":"gene"},{"created":"2020-05-20T21:03:55.807425+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: poc1b has been classified as Green List (High Evidence).","entity_name":"POC1B","entity_type":"gene"},{"created":"2020-05-20T21:03:52.931357+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POC1B were changed from  to Cone-rod dystrophy 20 (MIM#615973)","entity_name":"POC1B","entity_type":"gene"},{"created":"2020-05-20T21:03:03.290675+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POC1B were set to ","entity_name":"POC1B","entity_type":"gene"},{"created":"2020-05-20T21:02:32.870666+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POC1B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"POC1B","entity_type":"gene"},{"created":"2020-05-20T21:01:22.885859+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPGR as ready","entity_name":"RPGR","entity_type":"gene"},{"created":"2020-05-20T21:01:22.873590+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpgr has been classified as Green List (High Evidence).","entity_name":"RPGR","entity_type":"gene"},{"created":"2020-05-20T21:01:20.382520+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPGR were changed from  to Retinitis pigmentosa 3 (MIM#300029)","entity_name":"RPGR","entity_type":"gene"},{"created":"2020-05-20T21:00:52.514409+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPGR were set to ","entity_name":"RPGR","entity_type":"gene"},{"created":"2020-05-20T21:00:17.098489+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPGR was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"RPGR","entity_type":"gene"},{"created":"2020-05-20T20:58:38.227041+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PACS1 as ready","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:58:38.213370+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pacs1 has been classified as Green List (High Evidence).","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:58:33.685266+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PACS1 were changed from  to Schuurs-Hoeijmakers syndrome (MIM# 615009)","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:58:04.802183+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PACS1 were set to ","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:57:35.931646+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PACS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:57:06.218627+10:00","panel_name":"Autism","panel_id":51,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PACS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26842493, 23159249; Phenotypes: Schuurs-Hoeijmakers syndrome (MIM# 615009); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:56:25.489096+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PACS1 as ready","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:56:25.476534+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pacs1 has been classified as Green List (High Evidence).","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:56:22.483825+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PACS1 were changed from  to Schuurs-Hoeijmakers syndrome (MIM# 615009)","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:55:53.494008+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PACS1 were set to ","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:55:22.239604+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PACS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:54:46.881028+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.705","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PACS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26842493, 23159249; Phenotypes: Schuurs-Hoeijmakers syndrome (MIM# 615009); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:53:50.547881+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PACS1 as ready","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:53:50.534033+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pacs1 has been classified as Green List (High Evidence).","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:53:46.517038+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2640","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PACS1 were changed from  to Schuurs-Hoeijmakers syndrome (MIM# 615009)","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:53:14.310056+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2639","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PACS1 were set to ","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:52:40.099358+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2638","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PACS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:52:06.815961+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2637","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PACS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26842493, 23159249; Phenotypes: Schuurs-Hoeijmakers syndrome (MIM# 615009); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:50:55.419573+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2838","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PACS1 as ready","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:50:55.410745+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2838","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pacs1 has been classified as Green List (High Evidence).","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:50:48.060437+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2838","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PACS1 were changed from  to Schuurs-Hoeijmakers syndrome (MIM# 615009)","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:50:29.440456+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2837","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PACS1 were set to ","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:50:05.234786+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2836","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PACS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PACS1","entity_type":"gene"},{"created":"2020-05-20T20:49:20.786899+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2835","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC15A4 as ready","entity_name":"SLC15A4","entity_type":"gene"},{"created":"2020-05-20T20:49:20.775375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2835","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc15a4 has been classified as Red List (Low Evidence).","entity_name":"SLC15A4","entity_type":"gene"},{"created":"2020-05-20T20:49:11.875810+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2835","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC15A4 were set to ","entity_name":"SLC15A4","entity_type":"gene"},{"created":"2020-05-20T20:48:51.755599+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2834","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC15A4 as Red List (low evidence)","entity_name":"SLC15A4","entity_type":"gene"},{"created":"2020-05-20T20:48:51.740412+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2834","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc15a4 has been classified as Red List (Low Evidence).","entity_name":"SLC15A4","entity_type":"gene"}]}