{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ23809","CPTIC","CPT1P"],"biotype":"protein_coding","hgnc_id":"HGNC:18540","gene_name":"carnitine palmitoyltransferase 1C","omim_gene":["608846"],"alias_name":null,"gene_symbol":"CPT1C","hgnc_symbol":"CPT1C","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:50194155-50216988","ensembl_id":"ENSG00000169169"}},"GRch38":{"90":{"location":"19:49690898-49713731","ensembl_id":"ENSG00000169169"}}},"hgnc_date_symbol_changed":"2003-11-27"},"entity_type":"gene","entity_name":"CPT1C","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["25751282","30564185"],"evidence":["Yorkshire and North East GLH","Expert Review Green","NHS GMS","London North GLH"],"phenotypes":["?Spastic paraplegia 73, autosomal dominant, 616282, AD"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":568,"hash_id":null,"name":"Hereditary spastic paraplegia - childhood onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.179","version_created":"2019-09-30T12:40:08.803161Z","relevant_disorders":["Childhood onset hereditary spastic paraplegia;R61"],"stats":{"number_of_genes":98,"number_of_strs":10,"number_of_regions":0},"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."}]}},{"gene_data":{"alias":["FLJ23809","CPTIC","CPT1P"],"biotype":"protein_coding","hgnc_id":"HGNC:18540","gene_name":"carnitine palmitoyltransferase 1C","omim_gene":["608846"],"alias_name":null,"gene_symbol":"CPT1C","hgnc_symbol":"CPT1C","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:50194155-50216988","ensembl_id":"ENSG00000169169"}},"GRch38":{"90":{"location":"19:49690898-49713731","ensembl_id":"ENSG00000169169"}}},"hgnc_date_symbol_changed":"2003-11-27"},"entity_type":"gene","entity_name":"CPT1C","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["25751282","30564185"],"evidence":["Expert Review Amber","Yorkshire and North East GLH","NHS GMS","London North GLH"],"phenotypes":["?Spastic paraplegia 73, autosomal dominant, 616282"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":567,"hash_id":null,"name":"Hereditary spastic paraplegia - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"0.156","version_created":"2019-09-30T12:38:14.427158Z","relevant_disorders":["R60"],"stats":{"number_of_genes":97,"number_of_strs":10,"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)"}]}}]}