{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Hek8"],"biotype":"protein_coding","hgnc_id":"HGNC:3388","gene_name":"EPH receptor A4","omim_gene":["602188"],"alias_name":null,"gene_symbol":"EPHA4","hgnc_symbol":"EPHA4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:222282747-222438922","ensembl_id":"ENSG00000116106"}},"GRch38":{"90":{"location":"2:221418027-221574202","ensembl_id":"ENSG00000116106"}}},"hgnc_date_symbol_changed":"1992-10-02"},"entity_type":"gene","entity_name":"EPHA4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Expert list"],"phenotypes":[],"mode_of_inheritance":"Unknown","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"}]}}]}