{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PARG1"],"biotype":"protein_coding","hgnc_id":"HGNC:30207","gene_name":"Rho GTPase activating protein 29","omim_gene":["610496"],"alias_name":null,"gene_symbol":"ARHGAP29","hgnc_symbol":"ARHGAP29","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:94614544-94740624","ensembl_id":"ENSG00000137962"}},"GRch38":{"90":{"location":"1:94148988-94275068","ensembl_id":"ENSG00000137962"}}},"hgnc_date_symbol_changed":"2005-04-28"},"entity_type":"gene","entity_name":"ARHGAP29","confidence_level":"1","penetrance":"Incomplete","mode_of_pathogenicity":"","publications":["23008150","25704602","27350171","27369588","27033726","25512736","27350171","28029220","27033726"],"evidence":["Victorian Clinical Genetics Services","Expert Review Red","Research"],"phenotypes":["cleft lip with or without cleft palate","Cleft palate"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":81,"hash_id":"57acb8268f620364dc61afd3","name":"Clefting","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.59","version_created":"2019-09-03T09:03:20.170928Z","relevant_disorders":["Familial non-syndromic cleft lip and or familial cleft palate","Familial non-syndromic clefting","Syndromic cleft lip and or cleft palate","Syndromic clefting"],"stats":{"number_of_genes":258,"number_of_strs":0,"number_of_regions":5},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}