{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CCDC193"],"biotype":"protein_coding","hgnc_id":"HGNC:21460","gene_name":"mirror-image polydactyly 1","omim_gene":["606850"],"alias_name":null,"gene_symbol":"MIPOL1","hgnc_symbol":"MIPOL1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"14:37667118-38021566","ensembl_id":"ENSG00000151338"}},"GRch38":{"90":{"location":"14:37197913-37552361","ensembl_id":"ENSG00000151338"}}},"hgnc_date_symbol_changed":"2003-10-02"},"entity_type":"gene","entity_name":"MIPOL1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["11954550"],"evidence":["Expert Review Red","Other"],"phenotypes":["Mirror-image polydactyly of hands and feet"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}