{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HIGM2","CDA2","ARP2","AID"],"biotype":"protein_coding","hgnc_id":"HGNC:13203","gene_name":"activation induced cytidine deaminase","omim_gene":["605257"],"alias_name":null,"gene_symbol":"AICDA","hgnc_symbol":"AICDA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"12:8754762-8765467","ensembl_id":"ENSG00000111732"}},"GRch38":{"90":{"location":"12:8602166-8612871","ensembl_id":"ENSG00000111732"}}},"hgnc_date_symbol_changed":"2000-09-19"},"entity_type":"gene","entity_name":"AICDA","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","UKGTN","Radboud University Medical Center, Nijmegen","Illumina TruGenome Clinical Sequencing Services","Emory Genetics Laboratory","Expert list"],"phenotypes":["Immunodeficiency with hyper-IgM, type 2\t605258"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":176,"hash_id":"56ba026c22c1fc5025762b50","name":"Infantile enterocolitis & monogenic inflammatory bowel disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.16","version_created":"2017-11-05T02:37:20.171671Z","relevant_disorders":["Infantile enterocolitis and monogenic inflammatory bowel disease"],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["HIGM2","CDA2","ARP2","AID"],"biotype":"protein_coding","hgnc_id":"HGNC:13203","gene_name":"activation induced cytidine deaminase","omim_gene":["605257"],"alias_name":null,"gene_symbol":"AICDA","hgnc_symbol":"AICDA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:8754762-8765467","ensembl_id":"ENSG00000111732"}},"GRch38":{"90":{"location":"12:8602166-8612871","ensembl_id":"ENSG00000111732"}}},"hgnc_date_symbol_changed":"2000-09-19"},"entity_type":"gene","entity_name":"AICDA","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Emory Genetics Laboratory"],"phenotypes":["Early Onset Inflammatory Bowel Disease","Immunodeficiency with hyper-IgM, type 2 605258"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":33,"hash_id":"56ba026422c1fc5025762b4f","name":"Gastrointestinal epithelial barrier disorders","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.59","version_created":"2019-06-20T15:11:44.535737Z","relevant_disorders":[],"stats":{"number_of_genes":82,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["HIGM2","CDA2","ARP2","AID"],"biotype":"protein_coding","hgnc_id":"HGNC:13203","gene_name":"activation induced cytidine deaminase","omim_gene":["605257"],"alias_name":null,"gene_symbol":"AICDA","hgnc_symbol":"AICDA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:8754762-8765467","ensembl_id":"ENSG00000111732"}},"GRch38":{"90":{"location":"12:8602166-8612871","ensembl_id":"ENSG00000111732"}}},"hgnc_date_symbol_changed":"2000-09-19"},"entity_type":"gene","entity_name":"AICDA","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["12958596","21700883","27701145"],"evidence":["NHS GMS","North West GLH","London North GLH","IUIS Classification February 2018","Victorian Clinical Genetics Services","Expert Review Green","ESID Registry 20171117","GRID V2.0","GOSH PID v.8.0","A- or hypo-gammaglobulinaemia v1.25"],"phenotypes":["Immunodeficiency with hyper-IgM, type 2","Hyper IgM syndrome with lymphoid hyperplasia","Immunodeficiency with hyper-IgM, type 2, 605258","Primary Immune Deficiencies","CSR defects and Hyper IgM (HIGM) syndromes","Bacterial infections, enlarged lymph nodes and germinal centers","Predominantly Antibody Deficiencies"],"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."}]}}]}