{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ14697","YEA4"],"biotype":"protein_coding","hgnc_id":"HGNC:20584","gene_name":"solute carrier family 35 member B4","omim_gene":["610923"],"alias_name":null,"gene_symbol":"SLC35B4","hgnc_symbol":"SLC35B4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:133974084-134001803","ensembl_id":"ENSG00000205060"}},"GRch38":{"90":{"location":"7:134289332-134317051","ensembl_id":"ENSG00000205060"}}},"hgnc_date_symbol_changed":"2003-09-09"},"entity_type":"gene","entity_name":"SLC35B4","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"}]}}]}