{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PYPAF8","MATER","PAN11","CLR19.8"],"biotype":"protein_coding","hgnc_id":"HGNC:21269","gene_name":"NLR family pyrin domain containing 5","omim_gene":["609658"],"alias_name":["nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 5","maternal antigen that embryos require"],"gene_symbol":"NLRP5","hgnc_symbol":"NLRP5","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:56511092-56573179","ensembl_id":"ENSG00000171487"}},"GRch38":{"90":{"location":"19:55999726-56061813","ensembl_id":"ENSG00000171487"}}},"hgnc_date_symbol_changed":"2006-12-08"},"entity_type":"gene","entity_name":"NLRP5","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["26323243"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["Multilocus imprinting disorder"],"mode_of_inheritance":"","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"}]}}]}