{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CCBP1","GPD","Dfy","CD234"],"biotype":"protein_coding","hgnc_id":"HGNC:4035","gene_name":"atypical chemokine receptor 1 (Duffy blood group)","omim_gene":["613665"],"alias_name":["atypical chemokine receptor 1"],"gene_symbol":"ACKR1","hgnc_symbol":"ACKR1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:159173097-159176290","ensembl_id":"ENSG00000213088"}},"GRch38":{"90":{"location":"1:159203307-159206500","ensembl_id":"ENSG00000213088"}}},"hgnc_date_symbol_changed":"2014-04-04"},"entity_type":"gene","entity_name":"ACKR1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","NHS GMS","London South GLH"],"phenotypes":["613665 Benign hereditary neutropenia"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":519,"hash_id":null,"name":"Cytopenia - NOT Fanconi anaemia","disease_group":"","disease_sub_group":"","status":"public","version":"0.120","version_created":"2019-09-23T10:29:43.892929Z","relevant_disorders":["R91","R258"],"stats":{"number_of_genes":84,"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)"}]}}]}