{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SRm300","SRL300","KIAA0324","Cwc21"],"biotype":"protein_coding","hgnc_id":"HGNC:16639","gene_name":"serine/arginine repetitive matrix 2","omim_gene":["606032"],"alias_name":null,"gene_symbol":"SRRM2","hgnc_symbol":"SRRM2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:2802330-2822539","ensembl_id":"ENSG00000167978"}},"GRch38":{"90":{"location":"16:2752329-2772538","ensembl_id":"ENSG00000167978"}}},"hgnc_date_symbol_changed":"2001-09-24"},"entity_type":"gene","entity_name":"SRRM2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26135620"],"evidence":["Expert Review Red","Literature"],"phenotypes":["predisposition papillary thyroid carcinoma"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":171,"hash_id":"576cd7ca8f6203609632be82","name":"Inherited non-medullary thyroid cancer","disease_group":"Tumour syndromes","disease_sub_group":"Breast and endocrine","status":"public","version":"1.4","version_created":"2017-11-05T02:37:20.162547Z","relevant_disorders":[],"stats":{"number_of_genes":30,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}