{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MLTKalpha","MLTKbeta","ZAK","MLTK","MLK7","MRK"],"biotype":"protein_coding","hgnc_id":"HGNC:17797","gene_name":"mitogen-activated protein kinase kinase kinase 20","omim_gene":["609479"],"alias_name":["ZAK1 homolog, leucine zipper and sterile-alpha motif kinase (Dictyostelium)","mixed lineage kinase 7"],"gene_symbol":"MAP3K20","hgnc_symbol":"MAP3K20","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:173940163-174132738","ensembl_id":"ENSG00000091436"}},"GRch38":{"90":{"location":"2:173075435-173268010","ensembl_id":"ENSG00000091436"}}},"hgnc_date_symbol_changed":"2016-10-19"},"entity_type":"gene","entity_name":"MAP3K20","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["27816943"],"evidence":["Expert Review Green"],"phenotypes":["congenital myopathy with fibre type disproportion"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":465,"hash_id":null,"name":"Neuromuscular disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.11","version_created":"2019-10-09T12:42:27.875560Z","relevant_disorders":["Other rare neuromuscular disorders; R381"],"stats":{"number_of_genes":245,"number_of_strs":2,"number_of_regions":5},"types":[{"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":["MLTKalpha","MLTKbeta","ZAK","MLTK","MLK7","MRK"],"biotype":"protein_coding","hgnc_id":"HGNC:17797","gene_name":"mitogen-activated protein kinase kinase kinase 20","omim_gene":["609479"],"alias_name":["ZAK1 homolog, leucine zipper and sterile-alpha motif kinase (Dictyostelium)","mixed lineage kinase 7"],"gene_symbol":"MAP3K20","hgnc_symbol":"MAP3K20","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:173940163-174132738","ensembl_id":"ENSG00000091436"}},"GRch38":{"90":{"location":"2:173075435-173268010","ensembl_id":"ENSG00000091436"}}},"hgnc_date_symbol_changed":"2016-10-19"},"entity_type":"gene","entity_name":"MAP3K20","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27816943"],"evidence":["NHS GMS","London South GLH","Expert Review Green","UCL"],"phenotypes":["congenital myopathy with fibre type disproportion"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":225,"hash_id":"553f94b6bb5a1616e5ed459a","name":"Congenital myopathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.166","version_created":"2019-10-09T12:41:32.789611Z","relevant_disorders":["R81"],"stats":{"number_of_genes":100,"number_of_strs":2,"number_of_regions":3},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"}]}}]}