{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MTLRP","ghrelin","obestatin"],"biotype":"protein_coding","hgnc_id":"HGNC:18129","gene_name":"ghrelin and obestatin prepropeptide","omim_gene":["605353"],"alias_name":["prepro-appetite regulatory hormone"],"gene_symbol":"GHRL","hgnc_symbol":"GHRL","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:10327359-10334631","ensembl_id":"ENSG00000157017"}},"GRch38":{"90":{"location":"3:10285675-10292947","ensembl_id":"ENSG00000157017"}}},"hgnc_date_symbol_changed":"2006-01-05"},"entity_type":"gene","entity_name":"GHRL","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26211777"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hirschsprung disease (HSCR)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}