{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1014"],"biotype":"protein_coding","hgnc_id":"HGNC:19752","gene_name":"formin binding protein 4","omim_gene":["615265"],"alias_name":null,"gene_symbol":"FNBP4","hgnc_symbol":"FNBP4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:47738072-47788995","ensembl_id":"ENSG00000109920"}},"GRch38":{"90":{"location":"11:47716517-47767443","ensembl_id":"ENSG00000109920"}}},"hgnc_date_symbol_changed":"2002-11-25"},"entity_type":"gene","entity_name":"FNBP4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS"],"phenotypes":["Microphthalmia with Limb anomalies (Classified as variant of unknown significance on OMIM), 206920"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}}]}