{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:14376","gene_name":"acid phosphatase 4","omim_gene":["606362"],"alias_name":["testicular acid phosphatase"],"gene_symbol":"ACP4","hgnc_symbol":"ACP4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:51293672-51298481","ensembl_id":"ENSG00000142513"}},"GRch38":{"90":{"location":"19:50790415-50795224","ensembl_id":"ENSG00000142513"}}},"hgnc_date_symbol_changed":"2017-06-23"},"entity_type":"gene","entity_name":"ACP4","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28513613","27843125"],"evidence":["Expert Review Green","Other"],"phenotypes":["Amelogenesis imperfecta, type IJ,  617297","hypoplastic amelogenesis imperfecta"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":269,"hash_id":"58c7f3c78f620328d77ce70e","name":"Amelogenesis imperfecta","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"2.0","version_created":"2019-09-04T13:55:51.137280Z","relevant_disorders":["Amelogenesis Imperfecta","R340"],"stats":{"number_of_genes":39,"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."}]}}]}