{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:7562","gene_name":"myeloid differentiation primary response 88","omim_gene":["602170"],"alias_name":null,"gene_symbol":"MYD88","hgnc_symbol":"MYD88","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:38179969-38184513","ensembl_id":"ENSG00000172936"}},"GRch38":{"90":{"location":"3:38138478-38143022","ensembl_id":"ENSG00000172936"}}},"hgnc_date_symbol_changed":"1997-12-23"},"entity_type":"gene","entity_name":"MYD88","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear 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