{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HSL"],"biotype":"protein_coding","hgnc_id":"HGNC:6621","gene_name":"lipase E, hormone sensitive type","omim_gene":["151750"],"alias_name":null,"gene_symbol":"LIPE","hgnc_symbol":"LIPE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:42905659-42931578","ensembl_id":"ENSG00000079435"}},"GRch38":{"90":{"location":"19:42401507-42427426","ensembl_id":"ENSG00000079435"}}},"hgnc_date_symbol_changed":"1989-02-23"},"entity_type":"gene","entity_name":"LIPE","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["27862896","25475467","24848981"],"evidence":["Expert Review Green","Expert list"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":174,"hash_id":"55b2109c22c1fc7dd7ce411f","name":"Insulin resistance (including lipodystrophy)","disease_group":"Endocrine disorders","disease_sub_group":"Disorders of unusual phenotypes","status":"public","version":"1.11","version_created":"2019-06-20T15:15:09.915719Z","relevant_disorders":["Insulin resistance (including lipodystrophy"],"stats":{"number_of_genes":26,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["HSL"],"biotype":"protein_coding","hgnc_id":"HGNC:6621","gene_name":"lipase E, hormone sensitive type","omim_gene":["151750"],"alias_name":null,"gene_symbol":"LIPE","hgnc_symbol":"LIPE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:42905659-42931578","ensembl_id":"ENSG00000079435"}},"GRch38":{"90":{"location":"19:42401507-42427426","ensembl_id":"ENSG00000079435"}}},"hgnc_date_symbol_changed":"1989-02-23"},"entity_type":"gene","entity_name":"LIPE","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["27862896","25475467","24848981"],"evidence":["Expert Review Green","Expert Review","Expert list"],"phenotypes":["Lipodystrophy, familial partial, type 6, 615980"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":546,"hash_id":null,"name":"Lipodystrophy - childhood onset","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-07-31T14:52:46.595959Z","relevant_disorders":["R158"],"stats":{"number_of_genes":13,"number_of_strs":0,"number_of_regions":0},"types":[{"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":"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."}]}}]}
