{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:1544","gene_name":"cerebellin 2 precursor","omim_gene":["600433"],"alias_name":null,"gene_symbol":"CBLN2","hgnc_symbol":"CBLN2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"18:70203915-70305756","ensembl_id":"ENSG00000141668"}},"GRch38":{"90":{"location":"18:72536680-72638521","ensembl_id":"ENSG00000141668"}}},"hgnc_date_symbol_changed":"1995-03-06"},"entity_type":"gene","entity_name":"CBLN2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23502781"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":193,"hash_id":"58c7f8a78f62033482c42716","name":"Pulmonary arterial hypertension","disease_group":"Cardiovascular disorders","disease_sub_group":"Pulmonary heart disease","status":"public","version":"2.0","version_created":"2019-09-23T17:04:36.560383Z","relevant_disorders":["PAH","R188"],"stats":{"number_of_genes":18,"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":"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."}]}}]}