{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FBLP-1","CAL","migfilin"],"biotype":"protein_coding","hgnc_id":"HGNC:24686","gene_name":"filamin binding LIM protein 1","omim_gene":["607747"],"alias_name":null,"gene_symbol":"FBLIM1","hgnc_symbol":"FBLIM1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:16083102-16113089","ensembl_id":"ENSG00000162458"}},"GRch38":{"90":{"location":"1:15756607-15786594","ensembl_id":"ENSG00000162458"}}},"hgnc_date_symbol_changed":"2005-06-15"},"entity_type":"gene","entity_name":"FBLIM1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["29912021"],"evidence":["NHS GMS"],"phenotypes":["Majeed syndrome (Chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia) 609628"],"mode_of_inheritance":"","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"}]}}]}