{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ACLP"],"biotype":"protein_coding","hgnc_id":"HGNC:303","gene_name":"AE binding protein 1","omim_gene":["602981"],"alias_name":["aortic carboxypeptidase-like protein","adipocyte enhancer binding protein 1"],"gene_symbol":"AEBP1","hgnc_symbol":"AEBP1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:44143960-44154161","ensembl_id":"ENSG00000106624"}},"GRch38":{"90":{"location":"7:44104361-44114562","ensembl_id":"ENSG00000106624"}}},"hgnc_date_symbol_changed":"1998-03-06"},"entity_type":"gene","entity_name":"AEBP1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["29606302"],"evidence":["NHS GMS","Expert Review Green","Literature"],"phenotypes":["Ehlers-Danlos syndrome type","EDS type","Part of the EDS spectrum"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":53,"hash_id":"588728f38f62030cf7152165","name":"Ehlers Danlos syndromes","disease_group":"Rheumatological disorders","disease_sub_group":"Connective tissues disorders","status":"public","version":"2.1","version_created":"2019-10-09T07:04:44.655768Z","relevant_disorders":["Classical Ehlers Danlos Syndrome","Classical Ehlers-Danlos Syndrome","Ehlers-Danlos Syndrome (unusual phenotypes e.g. absent pain sense)","Ehlers-Danlos syndrome type 3","Kyphoscoliotic Ehlers-Danlos syndrome","EDS","Ehlers-Danlos syndromes","R101"],"stats":{"number_of_genes":75,"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","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."}]}}]}