{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["WIP"],"biotype":"protein_coding","hgnc_id":"HGNC:12736","gene_name":"WAS/WASL interacting protein family member 1","omim_gene":["602357"],"alias_name":null,"gene_symbol":"WIPF1","hgnc_symbol":"WIPF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:175424300-175547644","ensembl_id":"ENSG00000115935"}},"GRch38":{"90":{"location":"2:174559572-174682916","ensembl_id":"ENSG00000115935"}}},"hgnc_date_symbol_changed":"2006-10-12"},"entity_type":"gene","entity_name":"WIPF1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["22231303","9405671","11869681","14757742","27742395"],"evidence":["NHS GMS","North West GLH","London North GLH","Expert Review Green","IUIS Classification February 2018","Victorian Clinical Genetics Services","ESID Registry 20171117","GRID V2.0"],"phenotypes":["Wiskott-Aldrich syndrome like, WIP deficiency","WIP 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lymphohistiocytic disorders","Familial hemophagocytic lymphohistiocytic disorders","PID","Sepsis","Disseminated non-tuberculous mycobacterial infection","R15"],"stats":{"number_of_genes":395,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}},{"gene_data":{"alias":["WIP"],"biotype":"protein_coding","hgnc_id":"HGNC:12736","gene_name":"WAS/WASL interacting protein family member 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pseudoautosomal","tags":[],"panel":{"id":159,"hash_id":"58a70e858f62037e8779b2e8","name":"Cytopenias and congenital anaemias","disease_group":"Haematological disorders","disease_sub_group":"Anaemias and red cell disorders","status":"public","version":"1.73","version_created":"2019-09-23T11:25:32.403071Z","relevant_disorders":["Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria","Apparent aplastic anaemia or paroxysmal nocturnal haemoglobinuria","Congenital anaemias","Early onset pancytopenia and red cell disorders","Anaemias and red cell disorders","Cytopaenias and congenital anaemias","Cytopenia and pancytopenia"],"stats":{"number_of_genes":219,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["WIP"],"biotype":"protein_coding","hgnc_id":"HGNC:12736","gene_name":"WAS/WASL interacting protein family member 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pseudoautosomal","tags":[],"panel":{"id":519,"hash_id":null,"name":"Cytopenia - NOT Fanconi anaemia","disease_group":"","disease_sub_group":"","status":"public","version":"0.120","version_created":"2019-09-23T10:29:43.892929Z","relevant_disorders":["R91","R258"],"stats":{"number_of_genes":84,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"}]}}]}