{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ38979"],"biotype":"protein_coding","hgnc_id":"HGNC:30452","gene_name":"family with sequence similarity 92 member A","omim_gene":["617273"],"alias_name":null,"gene_symbol":"FAM92A","hgnc_symbol":"FAM92A","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:94710789-94743755","ensembl_id":"ENSG00000188343"}},"GRch38":{"90":{"location":"8:93698561-93731527","ensembl_id":"ENSG00000188343"}}},"hgnc_date_symbol_changed":"2016-09-30"},"entity_type":"gene","entity_name":"FAM92A","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["30395363"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["postaxial polydactyly type A9"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}