{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HBE"],"biotype":"protein_coding","hgnc_id":"HGNC:4830","gene_name":"hemoglobin subunit epsilon 1","omim_gene":["142100"],"alias_name":null,"gene_symbol":"HBE1","hgnc_symbol":"HBE1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:5289582-5526847","ensembl_id":"ENSG00000213931"}},"GRch38":{"90":{"location":"11:5268345-5505617","ensembl_id":"ENSG00000213931"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"HBE1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["17712794"],"evidence":["Expert Review Red","NHS GMS","London South GLH"],"phenotypes":["Epsilon-gamma-delta-beta thalassaemia"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":518,"hash_id":null,"name":"Rare anaemia","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-23T14:44:13.433190Z","relevant_disorders":["R92"],"stats":{"number_of_genes":94,"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":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}