{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIF10","PPP1R61"],"biotype":"protein_coding","hgnc_id":"HGNC:1856","gene_name":"centromere protein E","omim_gene":["117143"],"alias_name":["protein phosphatase 1, regulatory subunit 61"],"gene_symbol":"CENPE","hgnc_symbol":"CENPE","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:104026963-104119566","ensembl_id":"ENSG00000138778"}},"GRch38":{"90":{"location":"4:103105806-103198409","ensembl_id":"ENSG00000138778"}}},"hgnc_date_symbol_changed":"1994-07-04"},"entity_type":"gene","entity_name":"CENPE","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert list","Other"],"phenotypes":["?Microcephaly 13, primary, autosomal recessive, 616051","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."}]}}]}