{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ32099"],"biotype":"protein_coding","hgnc_id":"HGNC:29122","gene_name":"VPS8, CORVET complex subunit","omim_gene":null,"alias_name":null,"gene_symbol":"VPS8","hgnc_symbol":"VPS8","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:184529931-184770402","ensembl_id":"ENSG00000156931"}},"GRch38":{"90":{"location":"3:184812143-185052614","ensembl_id":"ENSG00000156931"}}},"hgnc_date_symbol_changed":"2006-07-07"},"entity_type":"gene","entity_name":"VPS8","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26752647","8969229","23840658"],"evidence":["Expert Review Red","ClinGen"],"phenotypes":["Arthrogryposis","OrphaNet ORPHA1037","OMIM108120"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":64,"hash_id":"58ee38f88f62033bda307d54","name":"ClinGen Gene Validity Curations","disease_group":"","disease_sub_group":"","status":"public","version":"0.64","version_created":"2019-06-20T15:10:34.572009Z","relevant_disorders":[],"stats":{"number_of_genes":47,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"ClinGen Curated genes","slug":"clingen-curated-genes","description":"ClinGen Curated genes"}]}},{"gene_data":{"alias":["FLJ32099"],"biotype":"protein_coding","hgnc_id":"HGNC:29122","gene_name":"VPS8, CORVET complex subunit","omim_gene":null,"alias_name":null,"gene_symbol":"VPS8","hgnc_symbol":"VPS8","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:184529931-184770402","ensembl_id":"ENSG00000156931"}},"GRch38":{"90":{"location":"3:184812143-185052614","ensembl_id":"ENSG00000156931"}}},"hgnc_date_symbol_changed":"2006-07-07"},"entity_type":"gene","entity_name":"VPS8","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26752647","8969229","23840658"],"evidence":["Expert Review Red","Other"],"phenotypes":["Arthrogryposis","OrphaNet ORPHA1037","OMIM108120"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":258,"hash_id":"55b75d5b22c1fc05fd2345c9","name":"Arthrogryposis","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"2.45","version_created":"2019-10-07T10:19:07.721001Z","relevant_disorders":["Arthrogrythsis"],"stats":{"number_of_genes":246,"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}