{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["B-50","PP46"],"biotype":"protein_coding","hgnc_id":"HGNC:4140","gene_name":"growth associated protein 43","omim_gene":["162060"],"alias_name":["neuron growth-associated protein 43","neuromodulin","nerve growth-related peptide GAP43","axonal membrane protein GAP-43","protein F1","calmodulin-binding protein P-57","neural phosphoprotein B-50"],"gene_symbol":"GAP43","hgnc_symbol":"GAP43","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:115342171-115440337","ensembl_id":"ENSG00000172020"}},"GRch38":{"90":{"location":"3:115623324-115721490","ensembl_id":"ENSG00000172020"}}},"hgnc_date_symbol_changed":"1990-07-10"},"entity_type":"gene","entity_name":"GAP43","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22325380"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hirschsprung disease","HD"],"mode_of_inheritance":"Unknown","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"}]}}]}