{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["RAP1"],"biotype":"protein_coding","hgnc_id":"HGNC:19246","gene_name":"TERF2 interacting protein","omim_gene":["605061"],"alias_name":null,"gene_symbol":"TERF2IP","hgnc_symbol":"TERF2IP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:75681684-75795770","ensembl_id":"ENSG00000166848"}},"GRch38":{"90":{"location":"16:75647786-75761872","ensembl_id":"ENSG00000166848"}}},"hgnc_date_symbol_changed":"2002-09-18"},"entity_type":"gene","entity_name":"TERF2IP","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":522,"hash_id":null,"name":"Familial melanoma","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-16T10:02:44.576997Z","relevant_disorders":["R254"],"stats":{"number_of_genes":8,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}