{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ31641","CMT2P"],"biotype":"protein_coding","hgnc_id":"HGNC:25135","gene_name":"leucine rich repeat and sterile alpha motif containing 1","omim_gene":["610933"],"alias_name":null,"gene_symbol":"LRSAM1","hgnc_symbol":"LRSAM1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"9:130213765-130265780","ensembl_id":"ENSG00000148356"}},"GRch38":{"90":{"location":"9:127451486-127503501","ensembl_id":"ENSG00000148356"}}},"hgnc_date_symbol_changed":"2003-12-19"},"entity_type":"gene","entity_name":"LRSAM1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22781092","28335037"],"evidence":["South West GLH","NHS GMS","London North GLH","Expert Review Green","Emory Genetics Laboratory","Radboud University Medical Center, Nijmegen","Expert list","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["Charcot Marie Toothe disease, axonal, type 2P, 614436","Charcot Marie Toothe disease, axonal, type 2P, 614436"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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."}]}}]}