{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CAP-H","hCAP-H"],"biotype":"protein_coding","hgnc_id":"HGNC:1112","gene_name":"non-SMC condensin I complex subunit H","omim_gene":["602332"],"alias_name":null,"gene_symbol":"NCAPH","hgnc_symbol":"NCAPH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:97001525-97039583","ensembl_id":"ENSG00000121152"}},"GRch38":{"90":{"location":"2:96335787-96373845","ensembl_id":"ENSG00000121152"}}},"hgnc_date_symbol_changed":"2006-09-04"},"entity_type":"gene","entity_name":"NCAPH","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["27737959"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["microcephaly"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}