{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ12681","JFP11","FLJ22302","TMEM112A"],"biotype":"protein_coding","hgnc_id":"HGNC:14154","gene_name":"lipase maturation factor 1","omim_gene":["611761"],"alias_name":null,"gene_symbol":"LMF1","hgnc_symbol":"LMF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:903634-1031318","ensembl_id":"ENSG00000103227"}},"GRch38":{"90":{"location":"16:853634-981318","ensembl_id":"ENSG00000103227"}}},"hgnc_date_symbol_changed":"2007-11-29"},"entity_type":"gene","entity_name":"LMF1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["17994020","19820022","30885219","30420299","29910226","22239554"],"evidence":["Expert Review Green","UKGTN","Eligibility statement prior genetic testing"],"phenotypes":["Lipase deficiency, combined, 246650"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":228,"hash_id":"57eab3658f620356ef5e4010","name":"Severe hypertriglyceridaemia","disease_group":"Cardiovascular disorders","disease_sub_group":"Arteriopathies","status":"public","version":"1.12","version_created":"2019-07-23T11:06:24.015746Z","relevant_disorders":[],"stats":{"number_of_genes":8,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["FLJ12681","JFP11","FLJ22302","TMEM112A"],"biotype":"protein_coding","hgnc_id":"HGNC:14154","gene_name":"lipase maturation factor 1","omim_gene":["611761"],"alias_name":null,"gene_symbol":"LMF1","hgnc_symbol":"LMF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:903634-1031318","ensembl_id":"ENSG00000103227"}},"GRch38":{"90":{"location":"16:853634-981318","ensembl_id":"ENSG00000103227"}}},"hgnc_date_symbol_changed":"2007-11-29"},"entity_type":"gene","entity_name":"LMF1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Emory Genetics Laboratory"],"phenotypes":["Hypercholesterolemia"],"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"}]}},{"gene_data":{"alias":["FLJ12681","JFP11","FLJ22302","TMEM112A"],"biotype":"protein_coding","hgnc_id":"HGNC:14154","gene_name":"lipase maturation factor 1","omim_gene":["611761"],"alias_name":null,"gene_symbol":"LMF1","hgnc_symbol":"LMF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:903634-1031318","ensembl_id":"ENSG00000103227"}},"GRch38":{"90":{"location":"16:853634-981318","ensembl_id":"ENSG00000103227"}}},"hgnc_date_symbol_changed":"2007-11-29"},"entity_type":"gene","entity_name":"LMF1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["17994020","19820022","30885219","30420299","29910226","22239554"],"evidence":["Expert Review Green","South West GLH","NHS GMS"],"phenotypes":["Lipase deficiency, combined 246650"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":527,"hash_id":null,"name":"Lipoprotein lipase deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-13T10:58:13.987962Z","relevant_disorders":["R324"],"stats":{"number_of_genes":10,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}