{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["RHOIP3","M-RIP","p116Rip"],"biotype":"protein_coding","hgnc_id":"HGNC:30321","gene_name":"myosin phosphatase Rho interacting protein","omim_gene":["612935"],"alias_name":["Rho interacting protein 3"],"gene_symbol":"MPRIP","hgnc_symbol":"MPRIP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:16945859-17120993","ensembl_id":"ENSG00000133030"}},"GRch38":{"90":{"location":"17:17042545-17217679","ensembl_id":"ENSG00000133030"}}},"hgnc_date_symbol_changed":"2008-06-02"},"entity_type":"gene","entity_name":"MPRIP","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"}]}}]}