{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TRM82","TRMT82"],"biotype":"protein_coding","hgnc_id":"HGNC:12756","gene_name":"WD repeat domain 4","omim_gene":["605924"],"alias_name":["TRM82 tRNA methyltransferase 82 homolog (S. cerevisiae)"],"gene_symbol":"WDR4","hgnc_symbol":"WDR4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"21:44263204-44299678","ensembl_id":"ENSG00000160193"}},"GRch38":{"90":{"location":"21:42843094-42879568","ensembl_id":"ENSG00000160193"}}},"hgnc_date_symbol_changed":"1999-07-19"},"entity_type":"gene","entity_name":"WDR4","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26416026","29597095"],"evidence":["NHS GMS","Expert Review Amber","Expert list"],"phenotypes":["MPD","microcephalic primordial dwarfism"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":162,"hash_id":"568f860222c1fc1c79ca1769","name":"Severe microcephaly","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"DNA repair disorders","status":"public","version":"1.72","version_created":"2019-08-19T16:58:29.143286Z","relevant_disorders":["Primary Microcephaly - Microcephalic Dwarfism Spectrum","Severe microcephaly"],"stats":{"number_of_genes":122,"number_of_strs":0,"number_of_regions":5},"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."}]}},{"gene_data":{"alias":["TRM82","TRMT82"],"biotype":"protein_coding","hgnc_id":"HGNC:12756","gene_name":"WD repeat domain 4","omim_gene":["605924"],"alias_name":["TRM82 tRNA methyltransferase 82 homolog (S. cerevisiae)"],"gene_symbol":"WDR4","hgnc_symbol":"WDR4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"21:44263204-44299678","ensembl_id":"ENSG00000160193"}},"GRch38":{"90":{"location":"21:42843094-42879568","ensembl_id":"ENSG00000160193"}}},"hgnc_date_symbol_changed":"1999-07-19"},"entity_type":"gene","entity_name":"WDR4","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["29597095","26416026"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Primordial dwarfism","motor and speech delay","intellectual disability","global developmental delay."],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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"}]}}]}