{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ20793","KIAA1830","PDIA13"],"biotype":"protein_coding","hgnc_id":"HGNC:24718","gene_name":"thioredoxin related transmembrane protein 3","omim_gene":["616102"],"alias_name":["protein disulfide isomerase family A, member 13"],"gene_symbol":"TMX3","hgnc_symbol":"TMX3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"18:66340925-66382535","ensembl_id":"ENSG00000166479"}},"GRch38":{"90":{"location":"18:68673688-68715298","ensembl_id":"ENSG00000166479"}}},"hgnc_date_symbol_changed":"2009-02-23"},"entity_type":"gene","entity_name":"TMX3","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["20485507"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Microphthalmia, coloboma, micrognathia, diaphragmatic hernia","None"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}}]}