{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ANILLIN","Scraps","scra"],"biotype":"protein_coding","hgnc_id":"HGNC:14082","gene_name":"anillin actin binding protein","omim_gene":["616027"],"alias_name":null,"gene_symbol":"ANLN","hgnc_symbol":"ANLN","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:36429415-36493400","ensembl_id":"ENSG00000011426"}},"GRch38":{"90":{"location":"7:36389806-36453791","ensembl_id":"ENSG00000011426"}}},"hgnc_date_symbol_changed":"2001-01-03"},"entity_type":"gene","entity_name":"ANLN","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24676636","30002222"],"evidence":["NHS GMS","Expert Review Amber","Literature"],"phenotypes":["Focal segmental glomerulosclerosis 8\t616032"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":106,"hash_id":"55af787822c1fc78a829f89f","name":"Proteinuric renal disease","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Syndromes with prominent renal abnormalities","status":"public","version":"1.225","version_created":"2019-10-09T10:57:45.692187Z","relevant_disorders":["R195"],"stats":{"number_of_genes":95,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"}]}}]}