{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CANP3","p94","nCL-1"],"biotype":"protein_coding","hgnc_id":"HGNC:1480","gene_name":"calpain 3","omim_gene":["114240"],"alias_name":null,"gene_symbol":"CAPN3","hgnc_symbol":"CAPN3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"15:42640301-42704516","ensembl_id":"ENSG00000092529"}},"GRch38":{"90":{"location":"15:42359500-42412318","ensembl_id":"ENSG00000092529"}}},"hgnc_date_symbol_changed":"1989-06-30"},"entity_type":"gene","entity_name":"CAPN3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["http://www.ncbi.nlm.nih.gov/books/NBK1408/"],"evidence":["Expert Review Green"],"phenotypes":["Muscular dystrophy, limb-girdle, type 2A, 253600","Limb-girdle muscular dystrophy","Limb-Girdle Muscular Dystrophy, Recessive"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":465,"hash_id":null,"name":"Neuromuscular disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.11","version_created":"2019-10-09T12:42:27.875560Z","relevant_disorders":["Other rare neuromuscular disorders; R381"],"stats":{"number_of_genes":245,"number_of_strs":2,"number_of_regions":5},"types":[{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["CANP3","p94","nCL-1"],"biotype":"protein_coding","hgnc_id":"HGNC:1480","gene_name":"calpain 3","omim_gene":["114240"],"alias_name":null,"gene_symbol":"CAPN3","hgnc_symbol":"CAPN3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"15:42640301-42704516","ensembl_id":"ENSG00000092529"}},"GRch38":{"90":{"location":"15:42359500-42412318","ensembl_id":"ENSG00000092529"}}},"hgnc_date_symbol_changed":"1989-06-30"},"entity_type":"gene","entity_name":"CAPN3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert list"],"phenotypes":[],"mode_of_inheritance":"","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"}]}},{"gene_data":{"alias":["CANP3","p94","nCL-1"],"biotype":"protein_coding","hgnc_id":"HGNC:1480","gene_name":"calpain 3","omim_gene":["114240"],"alias_name":null,"gene_symbol":"CAPN3","hgnc_symbol":"CAPN3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"15:42640301-42704516","ensembl_id":"ENSG00000092529"}},"GRch38":{"90":{"location":"15:42359500-42412318","ensembl_id":"ENSG00000092529"}}},"hgnc_date_symbol_changed":"1989-06-30"},"entity_type":"gene","entity_name":"CAPN3","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["http://www.ncbi.nlm.nih.gov/books/NBK1408/"],"evidence":["Expert Review Green","Eligibility statement prior genetic testing","Illumina TruGenome Clinical Sequencing Services","","Emory Genetics Laboratory","Radboud University Medical Center, Nijmegen"],"phenotypes":["Muscular dystrophy, limb-girdle, type 2A, 253600","Limb-Girdle Muscular Dystrophy, Recessive","Limb-girdle muscular dystrophy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":185,"hash_id":"55b7a65322c1fc05fc7a1869","name":"Limb girdle muscular dystrophy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.89","version_created":"2019-06-20T15:15:12.994579Z","relevant_disorders":[],"stats":{"number_of_genes":84,"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)"}]}}]}
