{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["RhoH","TTF"],"biotype":"protein_coding","hgnc_id":"HGNC:686","gene_name":"ras homolog family member H","omim_gene":["602037"],"alias_name":null,"gene_symbol":"RHOH","hgnc_symbol":"RHOH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:40192673-40248587","ensembl_id":"ENSG00000168421"}},"GRch38":{"90":{"location":"4:40191053-40246967","ensembl_id":"ENSG00000168421"}}},"hgnc_date_symbol_changed":"2004-03-24"},"entity_type":"gene","entity_name":"RHOH","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":562,"hash_id":null,"name":"Epidermodysplasia verruciformis","disease_group":"","disease_sub_group":"","status":"public","version":"0.9","version_created":"2019-09-09T15:38:35.409460Z","relevant_disorders":[],"stats":{"number_of_genes":7,"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["RhoH","TTF"],"biotype":"protein_coding","hgnc_id":"HGNC:686","gene_name":"ras homolog family member H","omim_gene":["602037"],"alias_name":null,"gene_symbol":"RHOH","hgnc_symbol":"RHOH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:40192673-40248587","ensembl_id":"ENSG00000168421"}},"GRch38":{"90":{"location":"4:40191053-40246967","ensembl_id":"ENSG00000168421"}}},"hgnc_date_symbol_changed":"2004-03-24"},"entity_type":"gene","entity_name":"RHOH","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["22850876","24189071"],"evidence":["Expert Review Amber","IUIS Classification February 2018","Victorian Clinical Genetics Services","ESID Registry 20171117","GRID V2.0"],"phenotypes":["RhoH deficiency","Combined immunodeficiency","Epidermodysplasia verruciformis","T cell deficiency and various infectious diseases","HPV infection, lung granulomas, molluscum contagiosum, lymphoma","Immunodeficiencies affecting cellular and humoral immunity"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":398,"hash_id":null,"name":"Primary immunodeficiency","disease_group":"","disease_sub_group":"","status":"public","version":"1.132","version_created":"2019-09-27T14:37:49.085568Z","relevant_disorders":["Primary immunodeficiency disorders","A- or hypo-gammaglobulinaemia","Congenital neutropaenia","Agranulocytosis","Combined B and T cell defect","Inherited complement deficiency","SCID","Primary immune disorder","Primary immunodeficiency","A-gammaglobulinaemia","Agammaglobulinaemia","hypo-gammaglobulinaemia","hypogammaglobulinemia","immune deficiency syndromes","Severe combined immunodeficiency","Congenital neutopenia","Familial haemophagocytic 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."}]}}]}