{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:6485","gene_name":"laminin subunit alpha 5","omim_gene":["601033"],"alias_name":null,"gene_symbol":"LAMA5","hgnc_symbol":"LAMA5","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:60883011-60942368","ensembl_id":"ENSG00000130702"}},"GRch38":{"90":{"location":"20:62307955-62367312","ensembl_id":"ENSG00000130702"}}},"hgnc_date_symbol_changed":"1997-10-30"},"entity_type":"gene","entity_name":"LAMA5","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["28544784"],"evidence":["NHS GMS","Wessex and West Midlands GLH"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":232,"hash_id":"553f94c2bb5a1616e5ed459c","name":"Congenital myaesthenic syndrome","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.52","version_created":"2019-08-07T14:24:09.650638Z","relevant_disorders":["Congenital myaesthenia","Congenital myasthenia"],"stats":{"number_of_genes":35,"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)"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:6485","gene_name":"laminin subunit alpha 5","omim_gene":["601033"],"alias_name":null,"gene_symbol":"LAMA5","hgnc_symbol":"LAMA5","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:60883011-60942368","ensembl_id":"ENSG00000130702"}},"GRch38":{"90":{"location":"20:62307955-62367312","ensembl_id":"ENSG00000130702"}}},"hgnc_date_symbol_changed":"1997-10-30"},"entity_type":"gene","entity_name":"LAMA5","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["29534211"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Nephrotic syndrome"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":106,"hash_id":"55af787822c1fc78a829f89f","name":"Proteinuric renal disease","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Syndromes with prominent renal abnormalities","status":"public","version":"1.225","version_created":"2019-10-09T10:57:45.692187Z","relevant_disorders":["R195"],"stats":{"number_of_genes":95,"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)"}]}}]}