{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ14668"],"biotype":"protein_coding","hgnc_id":"HGNC:25911","gene_name":"family with sequence similarity 136 member A","omim_gene":["616275"],"alias_name":["hypothetical protein FLJ14668"],"gene_symbol":"FAM136A","hgnc_symbol":"FAM136A","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:70523107-70529222","ensembl_id":"ENSG00000035141"}},"GRch38":{"90":{"location":"2:70295975-70302090","ensembl_id":"ENSG00000035141"}}},"hgnc_date_symbol_changed":"2007-07-10"},"entity_type":"gene","entity_name":"FAM136A","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010","25305078"],"evidence":["Expert Review Amber","Literature","Other"],"phenotypes":["Meniere disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist","multifactorial"],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}