{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KCa3.1","hSK4","hKCa4","hIKCa1","IK"],"biotype":"protein_coding","hgnc_id":"HGNC:6293","gene_name":"potassium calcium-activated channel subfamily N member 4","omim_gene":["602754"],"alias_name":["small conductance calcium-activated potassium channel 4","intermediate conductance calcium-activated potassium channel"],"gene_symbol":"KCNN4","hgnc_symbol":"KCNN4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:44270685-44285409","ensembl_id":"ENSG00000104783"}},"GRch38":{"90":{"location":"19:43766533-43781257","ensembl_id":"ENSG00000104783"}}},"hgnc_date_symbol_changed":"1998-04-07"},"entity_type":"gene","entity_name":"KCNN4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["26178367","26148990"],"evidence":["North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Expert Review Green","Wessex and West Midlands GLH"],"phenotypes":["616689 Dehydrated hereditary stomatocytosis 2","Hereditary Xerocytosis"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":518,"hash_id":null,"name":"Rare anaemia","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-23T14:44:13.433190Z","relevant_disorders":["R92"],"stats":{"number_of_genes":94,"number_of_strs":0,"number_of_regions":0},"types":[{"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)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}