{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HBZ1","HBZ-T1"],"biotype":"protein_coding","hgnc_id":"HGNC:4835","gene_name":"hemoglobin subunit zeta","omim_gene":["142310"],"alias_name":null,"gene_symbol":"HBZ","hgnc_symbol":"HBZ","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:202686-204502","ensembl_id":"ENSG00000130656"}},"GRch38":{"90":{"location":"16:152687-154503","ensembl_id":"ENSG00000130656"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"HBZ","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["9029003"],"evidence":["Expert Review Red","Other"],"phenotypes":["HEMOGLOBIN H HYDROPS FETALIS SYNDROME"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":144,"hash_id":"5763f4868f620350a199604f","name":"Fetal hydrops","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Fetal disorders","status":"public","version":"1.16","version_created":"2018-12-05T18:38:09.145885Z","relevant_disorders":[],"stats":{"number_of_genes":67,"number_of_strs":1,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}