{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PGT","OATP2A1"],"biotype":"protein_coding","hgnc_id":"HGNC:10955","gene_name":"solute carrier organic anion transporter family member 2A1","omim_gene":["601460"],"alias_name":null,"gene_symbol":"SLCO2A1","hgnc_symbol":"SLCO2A1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:133651540-133771028","ensembl_id":"ENSG00000174640"}},"GRch38":{"90":{"location":"3:133932696-134052184","ensembl_id":"ENSG00000174640"}}},"hgnc_date_symbol_changed":"2003-11-26"},"entity_type":"gene","entity_name":"SLCO2A1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","NHS GMS","Expert Review Green"],"phenotypes":["Hypertrophic osteoarthropathy, primary, autosomal recessive 2, 614441"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":557,"hash_id":null,"name":"Autosomal recessive primary hypertrophic osteoarthropathy","disease_group":"","disease_sub_group":"","status":"public","version":"0.11","version_created":"2019-06-20T15:14:56.570199Z","relevant_disorders":[],"stats":{"number_of_genes":3,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["PGT","OATP2A1"],"biotype":"protein_coding","hgnc_id":"HGNC:10955","gene_name":"solute carrier organic anion transporter family member 2A1","omim_gene":["601460"],"alias_name":null,"gene_symbol":"SLCO2A1","hgnc_symbol":"SLCO2A1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:133651540-133771028","ensembl_id":"ENSG00000174640"}},"GRch38":{"90":{"location":"3:133932696-134052184","ensembl_id":"ENSG00000174640"}}},"hgnc_date_symbol_changed":"2003-11-26"},"entity_type":"gene","entity_name":"SLCO2A1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Green",""],"phenotypes":["Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441","Hypertrophic osteoarthropathy, primary, autosomal recessive 2\t614441"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}