{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ10540","CT111"],"biotype":"protein_coding","hgnc_id":"HGNC:1161","gene_name":"centrosomal protein 55","omim_gene":["610000"],"alias_name":["cancer/testis antigen 111"],"gene_symbol":"CEP55","hgnc_symbol":"CEP55","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:95256389-95288849","ensembl_id":"ENSG00000138180"}},"GRch38":{"90":{"location":"10:93496632-93529092","ensembl_id":"ENSG00000138180"}}},"hgnc_date_symbol_changed":"2005-12-01"},"entity_type":"gene","entity_name":"CEP55","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28295209"],"evidence":["Literature"],"phenotypes":["Meckel-like syndrome"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":178,"hash_id":"55a76be222c1fc6710839b9f","name":"Primary ciliary disorders","disease_group":"Ciliopathies","disease_sub_group":"Respiratory ciliopathies","status":"public","version":"1.19","version_created":"2019-06-20T15:15:15.426107Z","relevant_disorders":["Primary ciliary dyskinesia"],"stats":{"number_of_genes":140,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}