{"count":221413,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1816","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1814","results":[{"created":"2020-04-29T15:55:23.068684+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Agree, structural brain abnormalities are a feature of more severe FKTN-associated disease, though PCH/cerebellar hypoplasia not prominent (more unusual abnormalities like cerebellar polymicrogyria described).","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-04-29T15:55:23.036168+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fktn has been classified as Amber List (Moderate Evidence).","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-04-29T15:53:59.131754+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKTN were changed from Cardiomyopathy, dilated, 1X\t611615; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4\t253800; Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4\t613152; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4\t611588; Walker-Warburg syndrome to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4\t253800; Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4\t613152; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4\t611588; Walker-Warburg syndrome","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-04-29T15:43:24.151146+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FKTN as Amber List (moderate evidence)","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-04-29T15:43:24.141635+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fktn has been classified as Amber List (Moderate Evidence).","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-04-29T15:30:39.499537+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GMPPB as ready","entity_name":"GMPPB","entity_type":"gene"},{"created":"2020-04-29T15:30:39.490317+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gmppb has been classified as Green List (High Evidence).","entity_name":"GMPPB","entity_type":"gene"},{"created":"2020-04-29T15:30:28.768885+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GMPPB as Green List (high evidence)","entity_name":"GMPPB","entity_type":"gene"},{"created":"2020-04-29T15:30:28.758196+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gmppb has been classified as Green List (High Evidence).","entity_name":"GMPPB","entity_type":"gene"},{"created":"2020-04-29T15:29:38.837084+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMT1 as ready","entity_name":"POMT1","entity_type":"gene"},{"created":"2020-04-29T15:29:38.828166+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomt1 has been classified as Green List (High Evidence).","entity_name":"POMT1","entity_type":"gene"},{"created":"2020-04-29T15:29:34.155411+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POMT1 as Green List (high evidence)","entity_name":"POMT1","entity_type":"gene"},{"created":"2020-04-29T15:29:34.141586+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomt1 has been classified as Green List (High Evidence).","entity_name":"POMT1","entity_type":"gene"},{"created":"2020-04-29T15:28:40.312524+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISPD as ready","entity_name":"ISPD","entity_type":"gene"},{"created":"2020-04-29T15:28:40.303653+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ispd has been classified as Green List (High Evidence).","entity_name":"ISPD","entity_type":"gene"},{"created":"2020-04-29T15:27:38.311043+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ISPD as Green List (high evidence)","entity_name":"ISPD","entity_type":"gene"},{"created":"2020-04-29T15:27:38.302748+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ispd has been classified as Green List (High Evidence).","entity_name":"ISPD","entity_type":"gene"},{"created":"2020-04-29T15:26:30.167198+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIAA1109 as ready","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2020-04-29T15:26:30.154720+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa1109 has been classified as Green List (High Evidence).","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2020-04-29T15:26:27.324640+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIAA1109 were changed from  to Alkuraya-Kucinskas syndrome, MIM# 617822","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2020-04-29T15:25:56.934831+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIAA1109 were set to ","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2020-04-29T15:25:25.470578+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIAA1109 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA1109","entity_type":"gene"},{"created":"2020-04-29T15:24:25.333949+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMGNT2 as ready","entity_name":"POMGNT2","entity_type":"gene"},{"created":"2020-04-29T15:24:25.324804+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomgnt2 has been classified as Green List (High Evidence).","entity_name":"POMGNT2","entity_type":"gene"},{"created":"2020-04-29T15:24:20.378393+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POMGNT2 as Green List (high evidence)","entity_name":"POMGNT2","entity_type":"gene"},{"created":"2020-04-29T15:24:20.369243+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomgnt2 has been classified as Green List (High Evidence).","entity_name":"POMGNT2","entity_type":"gene"},{"created":"2020-04-29T15:23:21.262953+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMGNT1 as ready","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2020-04-29T15:23:21.249149+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomgnt1 has been classified as Green List (High Evidence).","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2020-04-29T15:23:14.644285+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POMGNT1 as Green List (high evidence)","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2020-04-29T15:23:14.633750+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomgnt1 has been classified as Green List (High Evidence).","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2020-04-29T15:22:04.615647+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARGE1 as ready","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:22:04.603208+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: large1 has been classified as Green List (High Evidence).","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:22:00.814895+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARGE1 were set to PMID: 17878207; 19067344; PMID: 24709677","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:21:37.133771+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LARGE1 as Green List (high evidence)","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:21:37.123008+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: large1 has been classified as Green List (High Evidence).","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:20:57.152327+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: LARGE1.","entity_name":"LARGE1","entity_type":"gene"},{"created":"2020-04-29T15:16:15.545422+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MACF1 as ready","entity_name":"MACF1","entity_type":"gene"},{"created":"2020-04-29T15:16:15.536306+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Green List (High Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2020-04-29T15:16:08.814814+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MACF1 as Green List (high evidence)","entity_name":"MACF1","entity_type":"gene"},{"created":"2020-04-29T15:16:08.803290+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Green List (High Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2020-04-29T15:14:23.300680+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCOF1 as ready","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:14:23.288748+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcof1 has been classified as Green List (High Evidence).","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:14:19.034519+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCOF1 were changed from  to Treacher Collins syndrome 1, MIM# 154500","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:13:47.387591+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCOF1 were set to ","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:13:17.995736+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:12:45.250926+10:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TCOF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12444270, 15150774, 21951868; Phenotypes: Treacher Collins syndrome 1, MIM# 154500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:11:55.819566+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCOF1 as ready","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:11:55.808558+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcof1 has been classified as Green List (High Evidence).","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:11:46.924069+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCOF1 were changed from  to Treacher Collins syndrome 1, MIM# 154500","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:11:25.767497+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2657","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCOF1 were set to ","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:11:07.359441+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2656","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:10:24.516447+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2655","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TCOF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12444270, 15150774, 21951868; Phenotypes: Treacher Collins syndrome 1, MIM# 154500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:02:26.256893+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCOF1 as ready","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:02:26.238973+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcof1 has been classified as Green List (High Evidence).","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:02:23.780648+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCOF1 were changed from  to Treacher Collins syndrome 1, MIM# 154500","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:01:48.192058+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCOF1 were set to ","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T15:01:19.147601+10:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCOF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCOF1","entity_type":"gene"},{"created":"2020-04-29T14:59:55.758823+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: EMX2.","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:59:44.785921+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMX2 as ready","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:59:44.776721+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Amber List (Moderate Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:59:27.051658+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EMX2 were changed from  to Schizencephaly, MIM# 269160","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:58:53.196121+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2608","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EMX2 were set to ","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:58:17.763630+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2607","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EMX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:57:45.693609+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2606","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EMX2 as Amber List (moderate evidence)","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:57:45.684456+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2606","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Amber List (Moderate Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:57:01.306808+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2605","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EMX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:56:18.076928+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMX2 as ready","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:56:18.063825+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Red List (Low Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:56:15.071931+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EMX2 were changed from  to Schizencephaly, MIM# 269160","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:55:49.131101+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EMX2 were set to 8528262; 9359037; 9153481; 9153481; 18409201","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:55:24.004776+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EMX2 were set to ","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:55:03.956599+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EMX2 as Red List (low evidence)","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:55:03.944214+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Red List (Low Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:54:39.285606+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EMX2 as Red List (low evidence)","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:54:39.262354+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Red List (Low Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:54:07.249937+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EMX2: Rating: RED; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: None","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:52:46.968464+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EMX2 as ready","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:52:46.959174+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Amber List (Moderate Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:52:43.507609+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.689","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EMX2 were changed from  to Schizencephaly, MIM# 269160","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:52:05.496751+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: EMX2.","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:51:59.982157+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.688","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EMX2 were set to ","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:51:28.756548+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.687","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EMX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:50:59.805586+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.686","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EMX2 as Amber List (moderate evidence)","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:50:59.796526+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.686","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: emx2 has been classified as Amber List (Moderate Evidence).","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:49:53.576314+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2655","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: EMX2.","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:49:46.785314+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.685","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EMX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 8528262, 9359037, 9153481, 9153481, 18409201; Phenotypes: Schizencephaly, MIM# 269160; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EMX2","entity_type":"gene"},{"created":"2020-04-29T14:29:29.824734+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPAA1 as ready","entity_name":"GPAA1","entity_type":"gene"},{"created":"2020-04-29T14:29:29.815933+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpaa1 has been classified as Green List (High Evidence).","entity_name":"GPAA1","entity_type":"gene"},{"created":"2020-04-29T14:29:27.169497+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPAA1 were changed from  to Glycosylphosphatidylinositol biosynthesis defect 15, MIM# 617810","entity_name":"GPAA1","entity_type":"gene"},{"created":"2020-04-29T14:29:03.647100+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPAA1 were set to ","entity_name":"GPAA1","entity_type":"gene"},{"created":"2020-04-29T14:28:35.420103+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GPAA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GPAA1","entity_type":"gene"},{"created":"2020-04-29T14:26:15.392110+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPP1CB as ready","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:26:15.383095+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1cb has been classified as Red List (Low Evidence).","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:26:10.849569+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPP1CB were changed from  to Noonan syndrome-like disorder with loose anagen hair 2 (MIM#617506)","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:25:47.278614+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPP1CB were set to ","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:25:23.540643+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PPP1CB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:24:58.335954+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PPP1CB as Red List (low evidence)","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:24:58.327039+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1cb has been classified as Red List (Low Evidence).","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:24:28.726849+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PPP1CB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Noonan syndrome-like disorder with loose anagen hair 2 (MIM#617506); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PPP1CB","entity_type":"gene"},{"created":"2020-04-29T14:21:35.741255+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXP1 as ready","entity_name":"FOXP1","entity_type":"gene"}]}