{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ASP"],"biotype":"protein_coding","hgnc_id":"HGNC:745","gene_name":"agouti signaling protein","omim_gene":["600201"],"alias_name":["nonagouti homolog (mouse)"],"gene_symbol":"ASIP","hgnc_symbol":"ASIP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:32782375-32857150","ensembl_id":"ENSG00000101440"}},"GRch38":{"90":{"location":"20:34194569-34269344","ensembl_id":"ENSG00000101440"}}},"hgnc_date_symbol_changed":"1995-01-03"},"entity_type":"gene","entity_name":"ASIP","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","Expert Review Red","NHS GMS"],"phenotypes":["Pigmentation, susceptibility to facial pigmented spots"],"mode_of_inheritance":"","tags":[],"panel":{"id":559,"hash_id":null,"name":"Pigmentary skin disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-09-17T17:51:23.014209Z","relevant_disorders":[],"stats":{"number_of_genes":102,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}