{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:5201","gene_name":"heparan sulfate 6-O-sulfotransferase 1","omim_gene":["604846"],"alias_name":null,"gene_symbol":"HS6ST1","hgnc_symbol":"HS6ST1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:128994290-129076151","ensembl_id":"ENSG00000136720"}},"GRch38":{"90":{"location":"2:128236716-128318577","ensembl_id":"ENSG00000136720"}}},"hgnc_date_symbol_changed":"2002-08-23"},"entity_type":"gene","entity_name":"HS6ST1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21700882","26207952","23997646"],"evidence":["Expert Review Red","OMIM"],"phenotypes":["Hypogonadotropic hypogonadism 15 with or without anosmia, 614880"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["polygenic"],"panel":{"id":92,"hash_id":"573b204d8f62030defb98057","name":"Hypogonadotropic hypogonadism","disease_group":"Endocrine disorders","disease_sub_group":"Hypothalamic and pituitary disorders","status":"public","version":"1.26","version_created":"2019-06-20T15:11:57.281996Z","relevant_disorders":["Kallmann syndrome","Kallmann syndrom","Idiopathic hypogonadotropic hypogonadism"],"stats":{"number_of_genes":46,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}