{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CHAK1","LTRPC7","TRP-PLIK"],"biotype":"protein_coding","hgnc_id":"HGNC:17994","gene_name":"transient receptor potential cation channel subfamily M member 7","omim_gene":["605692"],"alias_name":null,"gene_symbol":"TRPM7","hgnc_symbol":"TRPM7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"15:50844670-50979012","ensembl_id":"ENSG00000092439"}},"GRch38":{"90":{"location":"15:50552473-50686815","ensembl_id":"ENSG00000092439"}}},"hgnc_date_symbol_changed":"2002-01-11"},"entity_type":"gene","entity_name":"TRPM7","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["27020697"],"evidence":["Expert Review Amber","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["macrothrombocytopenia"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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)"}]}}]}