{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ32752","FLJ46184","FLJ35709","DKFZp686J0796"],"biotype":"protein_coding","hgnc_id":"HGNC:26532","gene_name":"dynein heavy chain domain 1","omim_gene":["617277"],"alias_name":null,"gene_symbol":"DNHD1","hgnc_symbol":"DNHD1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:6518490-6614988","ensembl_id":"ENSG00000179532"}},"GRch38":{"90":{"location":"11:6497260-6593758","ensembl_id":"ENSG00000179532"}}},"hgnc_date_symbol_changed":"2005-11-28"},"entity_type":"gene","entity_name":"DNHD1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["No OMIM phenotype"],"mode_of_inheritance":"","tags":[],"panel":{"id":150,"hash_id":"568ea01e22c1fc1c78b6715d","name":"Rare multisystem ciliopathy disorders","disease_group":"Ciliopathies","disease_sub_group":"Congenital malformations caused by ciliopathies","status":"public","version":"1.121","version_created":"2019-09-26T13:15:06.802957Z","relevant_disorders":["Joubert syndrome","Bardet-Biedl Syndrome"],"stats":{"number_of_genes":201,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}