{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["dJ310O13.1"],"biotype":"protein_coding","hgnc_id":"HGNC:16118","gene_name":"tubulin tyrosine ligase like 9","omim_gene":null,"alias_name":null,"gene_symbol":"TTLL9","hgnc_symbol":"TTLL9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:30458505-30532764","ensembl_id":"ENSG00000131044"}},"GRch38":{"90":{"location":"20:31870702-31944963","ensembl_id":"ENSG00000131044"}}},"hgnc_date_symbol_changed":"2005-07-28"},"entity_type":"gene","entity_name":"TTLL9","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["23936318"],"evidence":["Literature"],"phenotypes":["anorectal malformation"],"mode_of_inheritance":"","tags":[],"panel":{"id":253,"hash_id":"576cd7e38f62036097d6cc9c","name":"Non-syndromic familial congenital anorectal malformations","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.5","version_created":"2019-06-20T15:15:14.416374Z","relevant_disorders":[],"stats":{"number_of_genes":51,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}