{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:9998","gene_name":"regulator of G protein signaling 2","omim_gene":["600861"],"alias_name":null,"gene_symbol":"RGS2","hgnc_symbol":"RGS2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:192778169-192781403","ensembl_id":"ENSG00000116741"}},"GRch38":{"90":{"location":"1:192809039-192812283","ensembl_id":"ENSG00000116741"}}},"hgnc_date_symbol_changed":"1994-11-01"},"entity_type":"gene","entity_name":"RGS2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["20403096","28784619"],"evidence":["Expert Review Amber","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":545,"hash_id":null,"name":"Bleeding and platelet disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.78","version_created":"2019-09-23T11:07:54.788299Z","relevant_disorders":["R90"],"stats":{"number_of_genes":111,"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)"}]}}]}