{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CKR-5","CC-CKR-5","CKR5","CD195","IDDM22"],"biotype":"protein_coding","hgnc_id":"HGNC:1606","gene_name":"C-C motif chemokine receptor 5 (gene/pseudogene)","omim_gene":["601373"],"alias_name":null,"gene_symbol":"CCR5","hgnc_symbol":"CCR5","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:46411633-46417697","ensembl_id":"ENSG00000160791"}},"GRch38":{"90":{"location":"3:46370854-46376206","ensembl_id":"ENSG00000160791"}}},"hgnc_date_symbol_changed":"1996-05-15"},"entity_type":"gene","entity_name":"CCR5","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"}]}}]}