{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1824","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1822","results":[{"created":"2020-04-21T18:38:04.180191+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAPPC6B as Red List (low evidence)","entity_name":"TRAPPC6B","entity_type":"gene"},{"created":"2020-04-21T18:38:04.168167+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc6b has been classified as Red List (Low Evidence).","entity_name":"TRAPPC6B","entity_type":"gene"},{"created":"2020-04-21T18:37:15.174358+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP55 as ready","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:37:15.165320+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep55 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:37:12.188026+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP55 were changed from  to Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 236500","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:36:44.979040+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP55 were set to ","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:36:16.438678+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP55 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:35:49.406230+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP55 as Amber List (moderate evidence)","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:35:49.397168+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep55 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP55","entity_type":"gene"},{"created":"2020-04-21T18:34:50.954537+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM5 as ready","entity_name":"TMEM5","entity_type":"gene"},{"created":"2020-04-21T18:34:50.943449+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem5 has been classified as Green List (High Evidence).","entity_name":"TMEM5","entity_type":"gene"},{"created":"2020-04-21T18:34:44.352693+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TMEM5 as Green List (high evidence)","entity_name":"TMEM5","entity_type":"gene"},{"created":"2020-04-21T18:34:44.343225+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem5 has been classified as Green List (High Evidence).","entity_name":"TMEM5","entity_type":"gene"},{"created":"2020-04-21T18:33:47.373811+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TINF2 as ready","entity_name":"TINF2","entity_type":"gene"},{"created":"2020-04-21T18:33:47.359734+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2020-04-21T18:33:43.523880+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TINF2 as Green List (high evidence)","entity_name":"TINF2","entity_type":"gene"},{"created":"2020-04-21T18:33:43.514931+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2020-04-21T18:32:51.534772+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2565","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CWF19L1 as ready","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:32:51.525921+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2565","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cwf19l1 has been classified as Green List (High Evidence).","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:32:43.369196+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2565","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CWF19L1 were changed from  to Spinocerebellar ataxia, autosomal recessive 17, MIM#616127; intellectual disability, developmental delay","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:32:19.530226+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2564","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CWF19L1 were set to ","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:31:21.791203+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2563","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CWF19L1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:31:02.475787+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2562","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CWF19L1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25361784, 15981765, 26197978, 27016154, 30167849; Phenotypes: Spinocerebellar ataxia, autosomal recessive 17, MIM#616127, intellectual disability, developmental delay; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:28:57.905868+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CWF19L1 as ready","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:28:57.893256+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cwf19l1 has been classified as Green List (High Evidence).","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:28:52.841917+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CWF19L1 as Green List (high evidence)","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:28:52.832062+10:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cwf19l1 has been classified as Green List (High Evidence).","entity_name":"CWF19L1","entity_type":"gene"},{"created":"2020-04-21T18:24:39.354366+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AHI1 as ready","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:24:39.345494+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahi1 has been classified as Amber List (Moderate Evidence).","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:24:36.826694+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AHI1 were changed from  to Joubert syndrome 3, MIM# 608629","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:24:08.349747+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AHI1 were set to ","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:23:39.115383+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AHI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:23:16.335945+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AHI1 as Amber List (moderate evidence)","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:23:16.327189+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahi1 has been classified as Amber List (Moderate Evidence).","entity_name":"AHI1","entity_type":"gene"},{"created":"2020-04-21T18:15:02.753233+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASTN1 as ready","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:15:02.744218+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: astn1 has been classified as Amber List (Moderate Evidence).","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:14:31.015246+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASTN1 were changed from  to Polymicrogyria; hypoplastic corpus callosum","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:13:12.647229+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ASTN1 were set to ","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:12:46.306210+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ASTN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:07:53.767452+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ASTN1 as Amber List (moderate evidence)","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:07:53.757820+10:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: astn1 has been classified as Amber List (Moderate Evidence).","entity_name":"ASTN1","entity_type":"gene"},{"created":"2020-04-21T18:05:41.360441+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Green List (high evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:05:41.351969+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:05:11.750294+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Two families reported.; to: Two families reported and two animal models.","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:05:02.908645+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: B4GAT1: Changed rating: GREEN; Changed publications: 23359570, 23877401, 23359570, 23217742","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:04:19.017162+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2562","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Green List (high evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:04:19.003566+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2562","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:03:58.132375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2561","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Two families reported.; to: Two families reported and two animal models.","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:03:44.193561+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2561","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: B4GAT1: Changed rating: GREEN; Changed publications: 23359570, 23877401, 23359570, 23217742","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:00:55.340912+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: B4GAT1: Changed rating: GREEN","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T18:00:49.187704+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Two families reported.; to: Two families reported and two animal models.","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:56:44.657419+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to 23359570; 23877401; 23359570; 23217742","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:34:47.120733+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to 23359570; 23877401","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:34:16.489405+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Green List (high evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:34:16.476569+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:48.105468+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Two families reported.; to: Two families and two animal models.","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:43.433918+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to 23359570; 23877401; 23359570; 23217742","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:38.496274+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: B4GAT1: Changed rating: GREEN; Changed publications: 23359570, 23877401, 23359570, 23217742","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:22.058983+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Green List (high evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:22.028522+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:21.936170+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GAT1 as ready","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:33:21.912753+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:32:54.997452+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to 23359570; 23877401","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:32:24.557784+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to 23359570; 23877401","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:32:04.084623+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Green List (high evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:32:04.071105+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Green List (High Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:31:12.741688+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GAT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23359570, 23877401, 23359570, 23217742; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:27:05.438792+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GAT1 as ready","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:27:05.425864+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:26:59.971866+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GAT1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:26:35.434813+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to ","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:26:06.387610+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:25:34.617251+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Amber List (moderate evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:25:34.604150+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:25:04.183100+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GAT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 23359570, 23877401; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:23:51.831679+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GAT1 as ready","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:23:51.821114+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:23:04.077263+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GAT1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:22:48.086743+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GAT1 as ready","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:22:48.074609+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:22:24.297038+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to ","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:22:00.809295+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:21:37.978592+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Amber List (moderate evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:21:37.965869+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:21:15.804911+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GAT1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:21:04.632513+10:00","panel_name":"Muscular dystrophy","panel_id":141,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GAT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 23359570, 23877401; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:20:29.163822+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2561","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GAT1 as ready","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:20:29.155217+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2561","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:20:21.476161+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2561","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GAT1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:20:05.213612+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2560","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to ","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:19:45.527979+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2559","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:19:26.809071+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2558","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Amber List (moderate evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:19:26.797354+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2558","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:19:06.190365+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2557","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GAT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 23359570, 23877401; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:18:24.349326+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GAT1 were set to ","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:17:55.908663+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:17:33.088445+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GAT1 as Amber List (moderate evidence)","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:17:33.079747+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4gat1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:17:00.034939+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GAT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 23359570, 23877401; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GAT1","entity_type":"gene"},{"created":"2020-04-21T17:16:14.102468+10:00","panel_name":"Lissencephaly and Band Heterotopia","panel_id":15,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GAT1 were changed from  to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287","entity_name":"B4GAT1","entity_type":"gene"}]}