{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1347","ATP2C1A","PMR1","SPCA1"],"biotype":"protein_coding","hgnc_id":"HGNC:13211","gene_name":"ATPase secretory pathway Ca2+ transporting 1","omim_gene":["604384"],"alias_name":["secretory pathway Ca2+/Mn2+ ATPase 1","calcium-transporting ATPase type 2C member 1"],"gene_symbol":"ATP2C1","hgnc_symbol":"ATP2C1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:130569439-130735556","ensembl_id":"ENSG00000017260"}},"GRch38":{"90":{"location":"3:130850595-131016712","ensembl_id":"ENSG00000017260"}}},"hgnc_date_symbol_changed":"2000-09-19"},"entity_type":"gene","entity_name":"ATP2C1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":554,"hash_id":null,"name":"Epidermolysis bullosa and congenital skin fragility","disease_group":"","disease_sub_group":"","status":"public","version":"0.16","version_created":"2019-09-17T18:43:54.606444Z","relevant_disorders":[],"stats":{"number_of_genes":46,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}