{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CD49b"],"biotype":"protein_coding","hgnc_id":"HGNC:6137","gene_name":"integrin subunit alpha 2","omim_gene":["192974"],"alias_name":["alpha 2 subunit of VLA-2 receptor"],"gene_symbol":"ITGA2","hgnc_symbol":"ITGA2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:52285156-52390609","ensembl_id":"ENSG00000164171"}},"GRch38":{"90":{"location":"5:52989326-53094779","ensembl_id":"ENSG00000164171"}}},"hgnc_date_symbol_changed":"1991-08-06"},"entity_type":"gene","entity_name":"ITGA2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["10590055"],"evidence":["Expert Review Red","North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["614200 ?Glycoprotein Ia deficiency"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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)"}]}}]}