{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ZCW4","FLJ11565"],"biotype":"protein_coding","hgnc_id":"HGNC:23485","gene_name":"MORC family CW-type zinc finger 4","omim_gene":["300970"],"alias_name":null,"gene_symbol":"MORC4","hgnc_symbol":"MORC4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:106057101-106243474","ensembl_id":"ENSG00000133131"}},"GRch38":{"90":{"location":"X:106813871-107000244","ensembl_id":"ENSG00000133131"}}},"hgnc_date_symbol_changed":"2005-06-15"},"entity_type":"gene","entity_name":"MORC4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["29884332","29173301","28754779","26820620","26784911","26002935","25253127","23143602","28754779","24002981"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":386,"hash_id":null,"name":"Pancreatitis","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-09-04T09:45:14.660178Z","relevant_disorders":["R175"],"stats":{"number_of_genes":16,"number_of_strs":0,"number_of_regions":0},"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)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}},{"gene_data":{"alias":["ZCW4","FLJ11565"],"biotype":"protein_coding","hgnc_id":"HGNC:23485","gene_name":"MORC family CW-type zinc finger 4","omim_gene":["300970"],"alias_name":null,"gene_symbol":"MORC4","hgnc_symbol":"MORC4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:106057101-106243474","ensembl_id":"ENSG00000133131"}},"GRch38":{"90":{"location":"X:106813871-107000244","ensembl_id":"ENSG00000133131"}}},"hgnc_date_symbol_changed":"2005-06-15"},"entity_type":"gene","entity_name":"MORC4","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26350204"],"evidence":["Expert Review Red"],"phenotypes":[],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","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"}]}}]}