{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0693","CREST"],"biotype":"protein_coding","hgnc_id":"HGNC:15592","gene_name":"SS18L1, nBAF chromatin remodeling complex subunit","omim_gene":["606472"],"alias_name":["calcium-responsive transactivator"],"gene_symbol":"SS18L1","hgnc_symbol":"SS18L1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:60718822-60757540","ensembl_id":"ENSG00000184402"}},"GRch38":{"90":{"location":"20:62143795-62182484","ensembl_id":"ENSG00000184402"}}},"hgnc_date_symbol_changed":"2001-04-26"},"entity_type":"gene","entity_name":"SS18L1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["23708140","24360741"],"evidence":["Expert Review Amber","NHS GMS","Yorkshire and North East GLH"],"phenotypes":["Amyotrophic lateral sclerosis 105400"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":474,"hash_id":null,"name":"Neurodegenerative disorders - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.106","version_created":"2019-09-20T16:19:10.101841Z","relevant_disorders":["R58"],"stats":{"number_of_genes":395,"number_of_strs":18,"number_of_regions":4},"types":[{"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."}]}}]}