{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NNT1","BSF3","CLC","NR6","CISS2","BSF-3","NNT-1"],"biotype":"protein_coding","hgnc_id":"HGNC:17412","gene_name":"cardiotrophin like cytokine factor 1","omim_gene":["607672"],"alias_name":["B-cell stimulating factor 3","cold-induced sweating syndrome 2","novel neurotrophin-1"],"gene_symbol":"CLCF1","hgnc_symbol":"CLCF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:67131639-67141648","ensembl_id":"ENSG00000175505"}},"GRch38":{"90":{"location":"11:67364168-67374177","ensembl_id":"ENSG00000175505"}}},"hgnc_date_symbol_changed":"2005-02-22"},"entity_type":"gene","entity_name":"CLCF1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert list"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":258,"hash_id":"55b75d5b22c1fc05fd2345c9","name":"Arthrogryposis","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"2.45","version_created":"2019-10-07T10:19:07.721001Z","relevant_disorders":["Arthrogrythsis"],"stats":{"number_of_genes":246,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}