{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["K-REV","RAL1B","DKFZp586H0723"],"biotype":"protein_coding","hgnc_id":"HGNC:9857","gene_name":"RAP1B, member of RAS oncogene family","omim_gene":["179530"],"alias_name":null,"gene_symbol":"RAP1B","hgnc_symbol":"RAP1B","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"12:69004619-69054372","ensembl_id":"ENSG00000127314"}},"GRch38":{"90":{"location":"12:68610839-68671901","ensembl_id":"ENSG00000127314"}}},"hgnc_date_symbol_changed":"1989-06-30"},"entity_type":"gene","entity_name":"RAP1B","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["PMID: 26280580"],"evidence":["Expert Review Red","Expert Review"],"phenotypes":["Kabuki-like syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":173,"hash_id":"5549d5c4bb5a1630f22d5886","name":"Kabuki syndrome","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Kabuki","status":"public","version":"1.2","version_created":"2017-11-05T02:37:20.165958Z","relevant_disorders":[],"stats":{"number_of_genes":4,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}