{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PC5","PC6","SPC6"],"biotype":"protein_coding","hgnc_id":"HGNC:8747","gene_name":"proprotein convertase subtilisin/kexin type 5","omim_gene":["600488"],"alias_name":null,"gene_symbol":"PCSK5","hgnc_symbol":"PCSK5","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"9:78505560-78977255","ensembl_id":"ENSG00000099139"}},"GRch38":{"90":{"location":"9:75890644-76362339","ensembl_id":"ENSG00000099139"}}},"hgnc_date_symbol_changed":"1993-10-19"},"entity_type":"gene","entity_name":"PCSK5","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["18519639"],"evidence":["Other"],"phenotypes":["cardiac, tracheoesophageal, anorectal, and anteroposterior patterning defects, exomphalos, hindlimb hypoplasia, presacral mass, renal and palatal agenesis, and pulmonary hypoplasia"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":5,"hash_id":"5763f3788f620350a199604a","name":"Currarino triad","disease_group":"","disease_sub_group":"","status":"public","version":"1.1","version_created":"2017-11-05T02:37:19.823394Z","relevant_disorders":[],"stats":{"number_of_genes":11,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}