{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["hbet1"],"biotype":"protein_coding","hgnc_id":"HGNC:14562","gene_name":"Bet1 golgi vesicular membrane trafficking protein","omim_gene":["605456"],"alias_name":["Golgi vesicular membrane trafficking protein p18","Bet1p homolog"],"gene_symbol":"BET1","hgnc_symbol":"BET1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:93592074-93633694","ensembl_id":"ENSG00000105829"}},"GRch38":{"90":{"location":"7:93962762-94004382","ensembl_id":"ENSG00000105829"}}},"hgnc_date_symbol_changed":"2001-04-05"},"entity_type":"gene","entity_name":"BET1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","London South GLH"],"phenotypes":["Congenital muscular dystrophy with epilepsy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":207,"hash_id":"55b117c022c1fc7dd7ce411c","name":"Congenital muscular dystrophy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.62","version_created":"2019-10-09T12:19:40.245789Z","relevant_disorders":[],"stats":{"number_of_genes":53,"number_of_strs":1,"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)"}]}}]}