{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["IFPS"],"biotype":"protein_coding","hgnc_id":"HGNC:33276","gene_name":"filaggrin family member 2","omim_gene":["616284"],"alias_name":null,"gene_symbol":"FLG2","hgnc_symbol":"FLG2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:152321211-152332482","ensembl_id":"ENSG00000143520"}},"GRch38":{"90":{"location":"1:152348735-152360006","ensembl_id":"ENSG00000143520"}}},"hgnc_date_symbol_changed":"2007-08-21"},"entity_type":"gene","entity_name":"FLG2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":555,"hash_id":null,"name":"Ichthyosis and erythrokeratoderma","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-09-09T15:38:37.080974Z","relevant_disorders":[],"stats":{"number_of_genes":64,"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"}]}},{"gene_data":{"alias":["IFPS"],"biotype":"protein_coding","hgnc_id":"HGNC:33276","gene_name":"filaggrin family member 2","omim_gene":["616284"],"alias_name":null,"gene_symbol":"FLG2","hgnc_symbol":"FLG2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:152321211-152332482","ensembl_id":"ENSG00000143520"}},"GRch38":{"90":{"location":"1:152348735-152360006","ensembl_id":"ENSG00000143520"}}},"hgnc_date_symbol_changed":"2007-08-21"},"entity_type":"gene","entity_name":"FLG2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}