{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PHT1","PTR4"],"biotype":"protein_coding","hgnc_id":"HGNC:23090","gene_name":"solute carrier family 15 member 4","omim_gene":["615806"],"alias_name":null,"gene_symbol":"SLC15A4","hgnc_symbol":"SLC15A4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:129277739-129308528","ensembl_id":"ENSG00000139370"}},"GRch38":{"90":{"location":"12:128793191-128823983","ensembl_id":"ENSG00000139370"}}},"hgnc_date_symbol_changed":"2003-09-09"},"entity_type":"gene","entity_name":"SLC15A4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["29261175"],"evidence":["Literature"],"phenotypes":["No OMIM number"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":483,"hash_id":null,"name":"Pituitary hormone deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-07-31T14:30:21.964840Z","relevant_disorders":["R159"],"stats":{"number_of_genes":50,"number_of_strs":0,"number_of_regions":0},"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":"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."}]}}]}