{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["GCSFR"],"biotype":"protein_coding","hgnc_id":"HGNC:2439","gene_name":"colony stimulating factor 3 receptor","omim_gene":["138971"],"alias_name":null,"gene_symbol":"CSF3R","hgnc_symbol":"CSF3R","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:36931644-36948879","ensembl_id":"ENSG00000119535"}},"GRch38":{"90":{"location":"1:36466043-36483278","ensembl_id":"ENSG00000119535"}}},"hgnc_date_symbol_changed":"1990-12-10"},"entity_type":"gene","entity_name":"CSF3R","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["24753537","26324699","29070147","19620628"],"evidence":["NHS GMS","North West GLH","London North GLH","IUIS Classification February 2018","Victorian Clinical Genetics Services","Expert Review Green","ESID Registry 20171117","GRID V2.0","Congenital neutropaenia v1.22"],"phenotypes":["Neutropenia, severe congenital, 7, autosomal recessive, 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mycobacterial infection","R15"],"stats":{"number_of_genes":395,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}},{"gene_data":{"alias":["GCSFR"],"biotype":"protein_coding","hgnc_id":"HGNC:2439","gene_name":"colony stimulating factor 3 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