{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PAFAH","LDL-PLA2"],"biotype":"protein_coding","hgnc_id":"HGNC:9040","gene_name":"phospholipase A2 group VII","omim_gene":["601690"],"alias_name":null,"gene_symbol":"PLA2G7","hgnc_symbol":"PLA2G7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:46671938-46703430","ensembl_id":"ENSG00000146070"}},"GRch38":{"90":{"location":"6:46704201-46735693","ensembl_id":"ENSG00000146070"}}},"hgnc_date_symbol_changed":"1999-09-20"},"entity_type":"gene","entity_name":"PLA2G7","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Radboud University Medical Center, Nijmegen"],"phenotypes":["Platelet-activating factor acetylhydrolase deficiency, 614278{Asthma, susceptibility to}, 600807{Atopy, susceptibility to}, 147050"],"mode_of_inheritance":"","tags":[],"panel":{"id":62,"hash_id":"553f95d0bb5a1616e5ed45c1","name":"Severe multi-system atopic disease with high IgE","disease_group":"Dermatological disorders","disease_sub_group":"Atopy","status":"public","version":"1.7","version_created":"2017-11-05T02:37:19.949470Z","relevant_disorders":[],"stats":{"number_of_genes":8,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}