{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["AR"],"biotype":"protein_coding","hgnc_id":"HGNC:381","gene_name":"aldo-keto reductase family 1 member B","omim_gene":["103880"],"alias_name":["aldose reductase"],"gene_symbol":"AKR1B1","hgnc_symbol":"AKR1B1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:134127102-134144036","ensembl_id":"ENSG00000085662"}},"GRch38":{"90":{"location":"7:134442350-134459284","ensembl_id":"ENSG00000085662"}}},"hgnc_date_symbol_changed":"1991-08-07"},"entity_type":"gene","entity_name":"AKR1B1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22544659"],"evidence":["Literature"],"phenotypes":["PHACE syndrome"],"mode_of_inheritance":"","tags":["deletions"],"panel":{"id":94,"hash_id":"5763f4408f620350a22bcce1","name":"PHACE(S) syndrome","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.1","version_created":"2017-11-05T02:37:20.018813Z","relevant_disorders":[],"stats":{"number_of_genes":6,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}