{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SUT2"],"biotype":"protein_coding","hgnc_id":"HGNC:14467","gene_name":"solute carrier family 26 member 7","omim_gene":["608479"],"alias_name":["Anion exchange transporter"],"gene_symbol":"SLC26A7","hgnc_symbol":"SLC26A7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:92221722-92410378","ensembl_id":"ENSG00000147606"}},"GRch38":{"90":{"location":"8:91209494-91398152","ensembl_id":"ENSG00000147606"}}},"hgnc_date_symbol_changed":"2001-01-25"},"entity_type":"gene","entity_name":"SLC26A7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["29546359","30333321"],"evidence":["Expert Review Green","East of England GLH"],"phenotypes":["Primary congenital hypothyroidism (dyshormonogenesis)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":31,"hash_id":"5763f2938f620350a1996046","name":"Congenital hypothyroidism","disease_group":"Endocrine disorders","disease_sub_group":"Thyroid disorders","status":"public","version":"2.0","version_created":"2019-07-31T13:52:41.584963Z","relevant_disorders":["Congenital hypothyroidism or thyroid agenesis","R145"],"stats":{"number_of_genes":34,"number_of_strs":0,"number_of_regions":2},"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."},{"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."}]}}]}