{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0172"],"biotype":"protein_coding","hgnc_id":"HGNC:27263","gene_name":"KN motif and ankyrin repeat domains 4","omim_gene":["614612"],"alias_name":null,"gene_symbol":"KANK4","hgnc_symbol":"KANK4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:62702651-62785085","ensembl_id":"ENSG00000132854"}},"GRch38":{"90":{"location":"1:62236979-62319414","ensembl_id":"ENSG00000132854"}}},"hgnc_date_symbol_changed":"2008-01-29"},"entity_type":"gene","entity_name":"KANK4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["25961457"],"evidence":["NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":106,"hash_id":"55af787822c1fc78a829f89f","name":"Proteinuric renal disease","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Syndromes with prominent renal abnormalities","status":"public","version":"1.225","version_created":"2019-10-09T10:57:45.692187Z","relevant_disorders":["R195"],"stats":{"number_of_genes":95,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"}]}}]}
