{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["H-Sema-L","CD108"],"biotype":"protein_coding","hgnc_id":"HGNC:10741","gene_name":"semaphorin 7A (John Milton Hagen blood group)","omim_gene":["607961"],"alias_name":["John Milton Hagen blood group","H-Sema K1"],"gene_symbol":"SEMA7A","hgnc_symbol":"SEMA7A","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"15:74701630-74726808","ensembl_id":"ENSG00000138623"}},"GRch38":{"90":{"location":"15:74409289-74434467","ensembl_id":"ENSG00000138623"}}},"hgnc_date_symbol_changed":"1999-06-25"},"entity_type":"gene","entity_name":"SEMA7A","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24522099"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Congenital hypogonadotropic hypogonadism"],"mode_of_inheritance":"Unknown","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"}]}}]}