{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PMX2A","CFEOM2"],"biotype":"protein_coding","hgnc_id":"HGNC:691","gene_name":"paired like homeobox 2a","omim_gene":["602753"],"alias_name":null,"gene_symbol":"PHOX2A","hgnc_symbol":"PHOX2A","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:71950121-71956708","ensembl_id":"ENSG00000165462"}},"GRch38":{"90":{"location":"11:72239077-72245664","ensembl_id":"ENSG00000165462"}}},"hgnc_date_symbol_changed":"2003-02-14"},"entity_type":"gene","entity_name":"PHOX2A","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["11600883","14597037","22311481"],"evidence":["Expert Review Green","Wessex and West Midlands GLH","Literature"],"phenotypes":["Fibrosis of extraocular muscles, congenital, 2 602078","Fibrosis of extraocular muscles, congenital, 2"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":512,"hash_id":null,"name":"Congenital fibrosis of the extraocular muscles","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-01T09:34:29.773019Z","relevant_disorders":["R46"],"stats":{"number_of_genes":6,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}