{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:1093","gene_name":"bisphosphoglycerate mutase","omim_gene":["613896"],"alias_name":null,"gene_symbol":"BPGM","hgnc_symbol":"BPGM","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:134331560-134364565","ensembl_id":"ENSG00000172331"}},"GRch38":{"90":{"location":"7:134646808-134679813","ensembl_id":"ENSG00000172331"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"BPGM","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27651169","25015942","5799137","1421379","15054810"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Erythrocytosis due to bisphosphoglycerate mutase deficiency"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":157,"hash_id":"58c7fba38f6203345887d4f5","name":"Hereditary Erythrocytosis","disease_group":"","disease_sub_group":"","status":"public","version":"1.1","version_created":"2017-11-05T02:37:20.137591Z","relevant_disorders":[],"stats":{"number_of_genes":13,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}