{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MT1-MMP"],"biotype":"protein_coding","hgnc_id":"HGNC:7160","gene_name":"matrix metallopeptidase 14","omim_gene":["600754"],"alias_name":["membrane type 1 metalloprotease"],"gene_symbol":"MMP14","hgnc_symbol":"MMP14","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"14:23305766-23318236","ensembl_id":"ENSG00000157227"}},"GRch38":{"90":{"location":"14:22836557-22849027","ensembl_id":"ENSG00000157227"}}},"hgnc_date_symbol_changed":"1994-11-20"},"entity_type":"gene","entity_name":"MMP14","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22922033"],"evidence":["Expert Review Red",""],"phenotypes":["Winchester syndrome 277950"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["MT1-MMP"],"biotype":"protein_coding","hgnc_id":"HGNC:7160","gene_name":"matrix metallopeptidase 14","omim_gene":["600754"],"alias_name":["membrane type 1 metalloprotease"],"gene_symbol":"MMP14","hgnc_symbol":"MMP14","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"14:23305766-23318236","ensembl_id":"ENSG00000157227"}},"GRch38":{"90":{"location":"14:22836557-22849027","ensembl_id":"ENSG00000157227"}}},"hgnc_date_symbol_changed":"1994-11-20"},"entity_type":"gene","entity_name":"MMP14","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["22922033"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["WINCHESTER SYNDROME"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}