{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["rootletin","ROLT"],"biotype":"protein_coding","hgnc_id":"HGNC:21299","gene_name":"ciliary rootlet coiled-coil, rootletin","omim_gene":["615776"],"alias_name":["rootletin, ciliary rootlet protein"],"gene_symbol":"CROCC","hgnc_symbol":"CROCC","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:17066768-17299474","ensembl_id":"ENSG00000058453"}},"GRch38":{"90":{"location":"1:16740273-16972979","ensembl_id":"ENSG00000058453"}}},"hgnc_date_symbol_changed":"2009-03-04"},"entity_type":"gene","entity_name":"CROCC","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28041643"],"evidence":["NHS GMS","Literature"],"phenotypes":["Retinitis pigmentosa"],"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."}]}}]}