{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["GM-CSF","GMCSF"],"biotype":"protein_coding","hgnc_id":"HGNC:2434","gene_name":"colony stimulating factor 2","omim_gene":["138960"],"alias_name":["sargramostim","molgramostin","granulocyte-macrophage colony stimulating factor"],"gene_symbol":"CSF2","hgnc_symbol":"CSF2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:131409483-131411859","ensembl_id":"ENSG00000164400"}},"GRch38":{"90":{"location":"5:132073790-132076170","ensembl_id":"ENSG00000164400"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"CSF2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}