{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ39502","CAMDI"],"biotype":"protein_coding","hgnc_id":"HGNC:26821","gene_name":"coiled-coil domain containing 141","omim_gene":["616031"],"alias_name":["coiled-coil protein associated with myosin II and DISC1"],"gene_symbol":"CCDC141","hgnc_symbol":"CCDC141","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:179694484-179914813","ensembl_id":"ENSG00000163492"}},"GRch38":{"90":{"location":"2:178830269-179050086","ensembl_id":"ENSG00000163492"}}},"hgnc_date_symbol_changed":"2007-07-10"},"entity_type":"gene","entity_name":"CCDC141","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["28324054","27014940"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Normosmic IHH (no OMIM)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":92,"hash_id":"573b204d8f62030defb98057","name":"Hypogonadotropic hypogonadism","disease_group":"Endocrine disorders","disease_sub_group":"Hypothalamic and pituitary disorders","status":"public","version":"1.26","version_created":"2019-06-20T15:11:57.281996Z","relevant_disorders":["Kallmann syndrome","Kallmann syndrom","Idiopathic hypogonadotropic hypogonadism"],"stats":{"number_of_genes":46,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}