{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["LCAD","ACAD4"],"biotype":"protein_coding","hgnc_id":"HGNC:88","gene_name":"acyl-CoA dehydrogenase long chain","omim_gene":["609576"],"alias_name":null,"gene_symbol":"ACADL","hgnc_symbol":"ACADL","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:211052663-211090215","ensembl_id":"ENSG00000115361"}},"GRch38":{"90":{"location":"2:210187939-210225491","ensembl_id":"ENSG00000115361"}}},"hgnc_date_symbol_changed":"1988-11-07"},"entity_type":"gene","entity_name":"ACADL","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["doi: 10.1038/ng.507","PMC3773904"],"evidence":["Expert Review Red","Emory Genetics Laboratory"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":267,"hash_id":"5548cc07bb5a16250cc22015","name":"Hyperammonaemia","disease_group":"Metabolic disorders","disease_sub_group":"Urea Cycle disorders","status":"public","version":"1.8","version_created":"2017-11-05T02:37:20.328985Z","relevant_disorders":[],"stats":{"number_of_genes":106,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}