{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ38547","PGR21"],"biotype":"protein_coding","hgnc_id":"HGNC:13839","gene_name":"adhesion G protein-coupled receptor A3","omim_gene":["612303"],"alias_name":null,"gene_symbol":"ADGRA3","hgnc_symbol":"ADGRA3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:22346694-22517677","ensembl_id":"ENSG00000152990"}},"GRch38":{"90":{"location":"4:22345071-22516054","ensembl_id":"ENSG00000152990"}}},"hgnc_date_symbol_changed":"2015-03-03"},"entity_type":"gene","entity_name":"ADGRA3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["PMID: 23105016 identified a novel missense variant in a conserved residue in a Saudi Arabian family with nonsyndromic retinal pigmentosa."],"evidence":["NHS GMS","Expert Review Red"],"phenotypes":["No OMIM phenotype"],"mode_of_inheritance":"","tags":[],"panel":{"id":307,"hash_id":"56e0238b22c1fc09c97a6e46","name":"Retinal disorders","disease_group":"Ophthalmological disorders","disease_sub_group":"Posterior segment abnormalities","status":"public","version":"1.199","version_created":"2019-10-08T09:22:18.436205Z","relevant_disorders":["Posterior segment abnormalities","Cone Dysfunction Syndrome","Developmental macular and foveal dystrophy","Inherited macular dystrophy","Leber Congenital Amaurosis Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy","Rod Dysfunction Syndrome","Rod-cone dystrophy","Familial exudative vitreoretinopathy","Familial exudative retinopathy","R32","R33","R34","R35"],"stats":{"number_of_genes":320,"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."}]}}]}