{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1517","MGC4322","MGC2695","Dhr1"],"biotype":"protein_coding","hgnc_id":"HGNC:17210","gene_name":"DEAH-box helicase 37","omim_gene":["617362"],"alias_name":null,"gene_symbol":"DHX37","hgnc_symbol":"DHX37","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:125431371-125473668","ensembl_id":"ENSG00000150990"}},"GRch38":{"90":{"location":"12:124946825-124989122","ensembl_id":"ENSG00000150990"}}},"hgnc_date_symbol_changed":"2003-06-20"},"entity_type":"gene","entity_name":"DHX37","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["31256877"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["Intellectual Disability and Central Nervous System anomalies"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"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"}]}}]}