{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ11785","RINT-1"],"biotype":"protein_coding","hgnc_id":"HGNC:21876","gene_name":"RAD50 interactor 1","omim_gene":["610089"],"alias_name":null,"gene_symbol":"RINT1","hgnc_symbol":"RINT1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:105172532-105208124","ensembl_id":"ENSG00000135249"}},"GRch38":{"90":{"location":"7:105532085-105567677","ensembl_id":"ENSG00000135249"}}},"hgnc_date_symbol_changed":"2006-03-02"},"entity_type":"gene","entity_name":"RINT1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["31204009"],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities"],"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"}]}}]}