{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DUP","MRP1"],"biotype":"protein_coding","hgnc_id":"HGNC:7326","gene_name":"mutS homolog 3","omim_gene":["600887"],"alias_name":["Divergent upstream protein","Mismatch repair protein 1"],"gene_symbol":"MSH3","hgnc_symbol":"MSH3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:79950467-80172279","ensembl_id":"ENSG00000113318"}},"GRch38":{"90":{"location":"5:80654648-80876460","ensembl_id":"ENSG00000113318"}}},"hgnc_date_symbol_changed":"1995-09-28"},"entity_type":"gene","entity_name":"MSH3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Research","Expert Review Red"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":254,"hash_id":"591444928f620348d4b20c16","name":"GI tract tumours","disease_group":"Tumour syndromes","disease_sub_group":"GI tract","status":"public","version":"1.18","version_created":"2019-08-05T14:17:21.117330Z","relevant_disorders":["GI tract tumours","Familial colon cancer","Multiple bowel polyps","Peutz-Jeghers syndrome","GI tract","Inherited colorectal cancer (with or without polyposis)"],"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"}]}},{"gene_data":{"alias":["DUP","MRP1"],"biotype":"protein_coding","hgnc_id":"HGNC:7326","gene_name":"mutS homolog 3","omim_gene":["600887"],"alias_name":["Divergent upstream protein","Mismatch repair protein 1"],"gene_symbol":"MSH3","hgnc_symbol":"MSH3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:79950467-80172279","ensembl_id":"ENSG00000113318"}},"GRch38":{"90":{"location":"5:80654648-80876460","ensembl_id":"ENSG00000113318"}}},"hgnc_date_symbol_changed":"1995-09-28"},"entity_type":"gene","entity_name":"MSH3","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":504,"hash_id":null,"name":"Inherited polyposis","disease_group":"","disease_sub_group":"","status":"public","version":"0.55","version_created":"2019-09-03T09:14:02.359574Z","relevant_disorders":["R211","R209"],"stats":{"number_of_genes":17,"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)"}]}}]}