{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HVH3"],"biotype":"protein_coding","hgnc_id":"HGNC:3071","gene_name":"dual specificity phosphatase 5","omim_gene":["603069"],"alias_name":null,"gene_symbol":"DUSP5","hgnc_symbol":"DUSP5","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:112257596-112271302","ensembl_id":"ENSG00000138166"}},"GRch38":{"90":{"location":"10:110497838-110511544","ensembl_id":"ENSG00000138166"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"DUSP5","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["18927432"],"evidence":["Other"],"phenotypes":["infantile hemangioma, somatic"],"mode_of_inheritance":"","tags":[],"panel":{"id":94,"hash_id":"5763f4408f620350a22bcce1","name":"PHACE(S) syndrome","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.1","version_created":"2017-11-05T02:37:20.018813Z","relevant_disorders":[],"stats":{"number_of_genes":6,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}