{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NMB","HGFIN"],"biotype":"protein_coding","hgnc_id":"HGNC:4462","gene_name":"glycoprotein nmb","omim_gene":["604368"],"alias_name":["transmembrane glycoprotein","glycoprotein NMB","glycoprotein nmb-like protein","osteoactivin","hematopoietic growth factor inducible neurokinin-1","glycoprotein nonmetastatic melanoma protein B"],"gene_symbol":"GPNMB","hgnc_symbol":"GPNMB","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:23275586-23314727","ensembl_id":"ENSG00000136235"}},"GRch38":{"90":{"location":"7:23235967-23275108","ensembl_id":"ENSG00000136235"}}},"hgnc_date_symbol_changed":"1999-10-26"},"entity_type":"gene","entity_name":"GPNMB","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","NHS GMS","Expert Review Green"],"phenotypes":["AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3, 617920"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":559,"hash_id":null,"name":"Pigmentary skin disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-09-17T17:51:23.014209Z","relevant_disorders":[],"stats":{"number_of_genes":102,"number_of_strs":0,"number_of_regions":1},"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"}]}}]}