{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:19966","gene_name":"unc-79 homolog, NALCN channel complex subunit","omim_gene":["616884"],"alias_name":null,"gene_symbol":"UNC79","hgnc_symbol":"UNC79","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"14:93799565-94174222","ensembl_id":"ENSG00000133958"}},"GRch38":{"90":{"location":"14:93333219-93707876","ensembl_id":"ENSG00000133958"}}},"hgnc_date_symbol_changed":"2011-08-18"},"entity_type":"gene","entity_name":"UNC79","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}}]}