{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:10906","gene_name":"solute carrier family 10 member 2","omim_gene":["601295"],"alias_name":null,"gene_symbol":"SLC10A2","hgnc_symbol":"SLC10A2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:103696350-103719196","ensembl_id":"ENSG00000125255"}},"GRch38":{"90":{"location":"13:103043998-103066846","ensembl_id":"ENSG00000125255"}}},"hgnc_date_symbol_changed":"1995-10-24"},"entity_type":"gene","entity_name":"SLC10A2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["9109432"],"evidence":["Expert Review Red","Emory Genetics Laboratory"],"phenotypes":["Bile acid malabsorption, primary 613291"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":385,"hash_id":null,"name":"Neonatal cholestasis","disease_group":"Gastroenterological disorders","disease_sub_group":"Liver disease","status":"public","version":"1.4","version_created":"2019-06-20T15:13:26.764332Z","relevant_disorders":[],"stats":{"number_of_genes":90,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}