{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CD106"],"biotype":"protein_coding","hgnc_id":"HGNC:12663","gene_name":"vascular cell adhesion molecule 1","omim_gene":["192225"],"alias_name":null,"gene_symbol":"VCAM1","hgnc_symbol":"VCAM1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:101185298-101204601","ensembl_id":"ENSG00000162692"}},"GRch38":{"90":{"location":"1:100719742-100739045","ensembl_id":"ENSG00000162692"}}},"hgnc_date_symbol_changed":"1991-07-10"},"entity_type":"gene","entity_name":"VCAM1","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 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"}]}}]}