{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["frpHE","FRP-4","FRPHE","FRZB-2"],"biotype":"protein_coding","hgnc_id":"HGNC:10778","gene_name":"secreted frizzled related protein 4","omim_gene":["606570"],"alias_name":null,"gene_symbol":"SFRP4","hgnc_symbol":"SFRP4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:37945543-38065297","ensembl_id":"ENSG00000106483"}},"GRch38":{"90":{"location":"7:37905932-38025695","ensembl_id":"ENSG00000106483"}}},"hgnc_date_symbol_changed":"1998-07-15"},"entity_type":"gene","entity_name":"SFRP4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["27355534","27117872","24096177","26273529","22965941","22387305","20174869","27117872","28100910"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Pyle disease, 265900","PYL","Metaphyseal dysplasia"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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"}]}},{"gene_data":{"alias":["frpHE","FRP-4","FRPHE","FRZB-2"],"biotype":"protein_coding","hgnc_id":"HGNC:10778","gene_name":"secreted frizzled related protein 4","omim_gene":["606570"],"alias_name":null,"gene_symbol":"SFRP4","hgnc_symbol":"SFRP4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:37945543-38065297","ensembl_id":"ENSG00000106483"}},"GRch38":{"90":{"location":"7:37905932-38025695","ensembl_id":"ENSG00000106483"}}},"hgnc_date_symbol_changed":"1998-07-15"},"entity_type":"gene","entity_name":"SFRP4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["27355534","26273529","20174869","27117872","22965941","28100910","24096177","22387305"],"evidence":["NHS GMS","Expert Review Green","Literature"],"phenotypes":["PYL","Metaphyseal dysplasia","Pyle disease 265900"],"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"}]}}]}
