{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["P31","Vma4","ATP6E2"],"biotype":"protein_coding","hgnc_id":"HGNC:857","gene_name":"ATPase H+ transporting V1 subunit E1","omim_gene":["108746"],"alias_name":null,"gene_symbol":"ATP6V1E1","hgnc_symbol":"ATP6V1E1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:18074902-18111584","ensembl_id":"ENSG00000131100"}},"GRch38":{"90":{"location":"22:17592136-17628818","ensembl_id":"ENSG00000131100"}}},"hgnc_date_symbol_changed":"2002-06-21"},"entity_type":"gene","entity_name":"ATP6V1E1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["28065471"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal Recessive Cutis Laxa"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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"}]}}]}