{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3672","gene_name":"fibroblast growth factor 16","omim_gene":["300827"],"alias_name":null,"gene_symbol":"FGF16","hgnc_symbol":"FGF16","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:76709648-76712769","ensembl_id":"ENSG00000196468"}},"GRch38":{"90":{"location":"X:77447405-77457278","ensembl_id":"ENSG00000196468"}}},"hgnc_date_symbol_changed":"1998-12-22"},"entity_type":"gene","entity_name":"FGF16","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Expert list","Radboud University Medical Center, Nijmegen","UKGTN","Expert Review Green","London South East RGC GSTT","Viapath"],"phenotypes":["Metacarpal 4-5 fusion, 309630"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","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":[],"biotype":"protein_coding","hgnc_id":"HGNC:3672","gene_name":"fibroblast growth factor 16","omim_gene":["300827"],"alias_name":null,"gene_symbol":"FGF16","hgnc_symbol":"FGF16","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:76709648-76712769","ensembl_id":"ENSG00000196468"}},"GRch38":{"90":{"location":"X:77447405-77457278","ensembl_id":"ENSG00000196468"}}},"hgnc_date_symbol_changed":"1998-12-22"},"entity_type":"gene","entity_name":"FGF16","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Green","UKGTN","Expert list","Radboud University Medical Center, Nijmegen",""],"phenotypes":["Metacarpal 4-5 fusion 309630","Metacarpal 4-5 fusion\t309630"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","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"}]}}]}