{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CT-1","CT1"],"biotype":"protein_coding","hgnc_id":"HGNC:2499","gene_name":"cardiotrophin 1","omim_gene":["600435"],"alias_name":null,"gene_symbol":"CTF1","hgnc_symbol":"CTF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:30907928-30914881","ensembl_id":"ENSG00000150281"}},"GRch38":{"90":{"location":"16:30896607-30903560","ensembl_id":"ENSG00000150281"}}},"hgnc_date_symbol_changed":"1995-05-01"},"entity_type":"gene","entity_name":"CTF1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","Expert list","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":47,"hash_id":"55a4d99022c1fc6710839b84","name":"Dilated Cardiomyopathy and conduction defects","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.63","version_created":"2019-09-30T12:02:00.646768Z","relevant_disorders":["Dilated Cardiomyopathy","Dilated Cardiomyopathy (DCM)","Dilated cardiomyopathy - teen and adult"],"stats":{"number_of_genes":84,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CT-1","CT1"],"biotype":"protein_coding","hgnc_id":"HGNC:2499","gene_name":"cardiotrophin 1","omim_gene":["600435"],"alias_name":null,"gene_symbol":"CTF1","hgnc_symbol":"CTF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:30907928-30914881","ensembl_id":"ENSG00000150281"}},"GRch38":{"90":{"location":"16:30896607-30903560","ensembl_id":"ENSG00000150281"}}},"hgnc_date_symbol_changed":"1995-05-01"},"entity_type":"gene","entity_name":"CTF1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","Expert Review Red"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":749,"hash_id":null,"name":"Cardiomyopathies - including childhood onset","disease_group":"","disease_sub_group":"","status":"public","version":"0.13","version_created":"2019-09-16T12:01:25.928956Z","relevant_disorders":["Paediatric or syndromic cardiomyopathy","R135"],"stats":{"number_of_genes":180,"number_of_strs":0,"number_of_regions":1},"types":[{"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":"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)"}]}}]}