{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3011","gene_name":"dermatopontin","omim_gene":["125597"],"alias_name":null,"gene_symbol":"DPT","hgnc_symbol":"DPT","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:168664697-168698502","ensembl_id":"ENSG00000143196"}},"GRch38":{"90":{"location":"1:168695459-168729264","ensembl_id":"ENSG00000143196"}}},"hgnc_date_symbol_changed":"1993-08-24"},"entity_type":"gene","entity_name":"DPT","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["29095749","27876815"],"evidence":["Expert Review Amber","Literature"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["watchlist"],"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"}]}}]}