{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["IL-7"],"biotype":"protein_coding","hgnc_id":"HGNC:6023","gene_name":"interleukin 7","omim_gene":["146660"],"alias_name":null,"gene_symbol":"IL7","hgnc_symbol":"IL7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:79587978-79717758","ensembl_id":"ENSG00000104432"}},"GRch38":{"90":{"location":"8:78675743-78805523","ensembl_id":"ENSG00000104432"}}},"hgnc_date_symbol_changed":"1989-10-12"},"entity_type":"gene","entity_name":"IL7","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"}]}}]}