{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2908","gene_name":"delta like canonical Notch ligand 1","omim_gene":["606582"],"alias_name":null,"gene_symbol":"DLL1","hgnc_symbol":"DLL1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:170591294-170599561","ensembl_id":"ENSG00000198719"}},"GRch38":{"90":{"location":"6:170282206-170306565","ensembl_id":"ENSG00000198719"}}},"hgnc_date_symbol_changed":"2000-02-11"},"entity_type":"gene","entity_name":"DLL1","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27363716","21196490","29771000"],"evidence":["NHS GMS","Expert Review Amber","Literature"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist"],"panel":{"id":78,"hash_id":"568e87e022c1fc1c79ca1754","name":"Holoprosencephaly","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"1.23","version_created":"2019-09-30T12:37:25.593251Z","relevant_disorders":["Rhombencephalosynapsis","Holoprosencephaly - NOT chromosomal; R85"],"stats":{"number_of_genes":18,"number_of_strs":0,"number_of_regions":0},"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"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2908","gene_name":"delta like canonical Notch ligand 1","omim_gene":["606582"],"alias_name":null,"gene_symbol":"DLL1","hgnc_symbol":"DLL1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:170591294-170599561","ensembl_id":"ENSG00000198719"}},"GRch38":{"90":{"location":"6:170282206-170306565","ensembl_id":"ENSG00000198719"}}},"hgnc_date_symbol_changed":"2000-02-11"},"entity_type":"gene","entity_name":"DLL1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["31353024"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["INTELLECTUAL DISABILITY 616579"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}