{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MGCR1-PEN","MGCR1"],"biotype":"protein_coding","hgnc_id":"HGNC:7180","gene_name":"MN1 proto-oncogene, transcriptional regulator","omim_gene":["156100"],"alias_name":["probable tumor suppressor protein MN1"],"gene_symbol":"MN1","hgnc_symbol":"MN1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:28144265-28197486","ensembl_id":"ENSG00000169184"}},"GRch38":{"90":{"location":"22:27748277-27801498","ensembl_id":"ENSG00000169184"}}},"hgnc_date_symbol_changed":"1998-06-08"},"entity_type":"gene","entity_name":"MN1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["21242494"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["MN1 C-terminal truncation syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}