{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CRF","CRH1"],"biotype":"protein_coding","hgnc_id":"HGNC:2355","gene_name":"corticotropin releasing hormone","omim_gene":["122560"],"alias_name":["corticotropin-releasing factor","corticoliberin"],"gene_symbol":"CRH","hgnc_symbol":"CRH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:67088620-67090960","ensembl_id":"ENSG00000147571"}},"GRch38":{"90":{"location":"8:66176382-66178725","ensembl_id":"ENSG00000147571"}}},"hgnc_date_symbol_changed":"1988-08-31"},"entity_type":"gene","entity_name":"CRH","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Red","Expert"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":402,"hash_id":null,"name":"Genetic epilepsy syndromes","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Inherited Epilepsy Syndromes","status":"public","version":"1.363","version_created":"2019-10-08T10:06:11.607307Z","relevant_disorders":["Epilepsy Plus","Epilepsy plus other features","Genetic Epilepsy Syndromes","Epileptic encephalopathy","Familial Focal Epilepsies","Familial Genetic Generalised Epilepsies","Genetic Epilepsies with Febrile Seizures Plus (GEFS+)","Genetic Epilepsies with Febrile Seizures Plus"],"stats":{"number_of_genes":614,"number_of_strs":2,"number_of_regions":13},"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"}]}}]}