{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["P2X1"],"biotype":"protein_coding","hgnc_id":"HGNC:8533","gene_name":"purinergic receptor P2X 1","omim_gene":["600845"],"alias_name":null,"gene_symbol":"P2RX1","hgnc_symbol":"P2RX1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:3799886-3819794","ensembl_id":"ENSG00000108405"}},"GRch38":{"90":{"location":"17:3896592-3916500","ensembl_id":"ENSG00000108405"}}},"hgnc_date_symbol_changed":"1997-01-16"},"entity_type":"gene","entity_name":"P2RX1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["10816552"],"evidence":["Expert Review Amber","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Purinergic receptor P2X, ligand-gated ion channel, 1 DEFICIENCY"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":545,"hash_id":null,"name":"Bleeding and platelet disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.78","version_created":"2019-09-23T11:07:54.788299Z","relevant_disorders":["R90"],"stats":{"number_of_genes":111,"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)"}]}}]}