{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MIR","IDOL"],"biotype":"protein_coding","hgnc_id":"HGNC:21155","gene_name":"myosin regulatory light chain interacting protein","omim_gene":["610082"],"alias_name":["E3 ubiquitin ligase-inducible degrader of the low density lipoprotein receptor"],"gene_symbol":"MYLIP","hgnc_symbol":"MYLIP","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:16129356-16148479","ensembl_id":"ENSG00000007944"}},"GRch38":{"90":{"location":"6:16129125-16148248","ensembl_id":"ENSG00000007944"}}},"hgnc_date_symbol_changed":"2003-11-26"},"entity_type":"gene","entity_name":"MYLIP","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["PMID: 23433581"],"evidence":["Eligibility statement prior genetic testing"],"phenotypes":["Gene part of the Global Lipid Genetic Consortium 12-SNP LDL-C gene score calculation (Talmud et al, 2013)"],"mode_of_inheritance":"","tags":[],"panel":{"id":6,"hash_id":"561518be22c1fc212900fb84","name":"Familial hypercholesterolaemia","disease_group":"Cardiovascular disorders","disease_sub_group":"Arteriopathies","status":"public","version":"1.26","version_created":"2019-10-07T15:50:14.542064Z","relevant_disorders":["Familial Hypercholesterolaemia","Familial Hypercholesterolemia"],"stats":{"number_of_genes":43,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}