{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DLX8","BP1"],"biotype":"protein_coding","hgnc_id":"HGNC:2917","gene_name":"distal-less homeobox 4","omim_gene":["601911"],"alias_name":null,"gene_symbol":"DLX4","hgnc_symbol":"DLX4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:48046334-48052321","ensembl_id":"ENSG00000108813"}},"GRch38":{"90":{"location":"17:49968970-49974959","ensembl_id":"ENSG00000108813"}}},"hgnc_date_symbol_changed":"1996-08-07"},"entity_type":"gene","entity_name":"DLX4","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25954033"],"evidence":["Expert Review Amber"],"phenotypes":["?Orofacial cleft 15, 616788","nonsyndromic cleft/lip palate (CL/P)","OROFACIAL CLEFT 15","OFC15"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":81,"hash_id":"57acb8268f620364dc61afd3","name":"Clefting","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.59","version_created":"2019-09-03T09:03:20.170928Z","relevant_disorders":["Familial non-syndromic cleft lip and or familial cleft palate","Familial non-syndromic clefting","Syndromic cleft lip and or cleft palate","Syndromic clefting"],"stats":{"number_of_genes":258,"number_of_strs":0,"number_of_regions":5},"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"}]}}]}