{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:4265","gene_name":"growth hormone releasing hormone","omim_gene":["139190"],"alias_name":["sermorelin","somatocrinin","somatoliberin"],"gene_symbol":"GHRH","hgnc_symbol":"GHRH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:35879489-35890238","ensembl_id":"ENSG00000118702"}},"GRch38":{"90":{"location":"20:37251082-37261835","ensembl_id":"ENSG00000118702"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"GHRH","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["15155578"],"evidence":["Literature","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["?Isolated growth hormone deficiency due to defect in GHRF","No OMIM number"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":483,"hash_id":null,"name":"Pituitary hormone deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-07-31T14:30:21.964840Z","relevant_disorders":["R159"],"stats":{"number_of_genes":50,"number_of_strs":0,"number_of_regions":0},"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 signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}