{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1073"],"biotype":"protein_coding","hgnc_id":"HGNC:7450","gene_name":"myotubularin related protein 2","omim_gene":["603557"],"alias_name":["phosphatidylinositol-3-phosphatase","phosphoinositide-3-phosphatase"],"gene_symbol":"MTMR2","hgnc_symbol":"MTMR2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:95566046-95658479","ensembl_id":"ENSG00000087053"}},"GRch38":{"90":{"location":"11:95832882-95925315","ensembl_id":"ENSG00000087053"}}},"hgnc_date_symbol_changed":"1999-02-05"},"entity_type":"gene","entity_name":"MTMR2","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28509084","10802647"],"evidence":["South West GLH","NHS GMS","London North GLH","Expert Review Green","Emory Genetics Laboratory","UKGTN","Expert list","Radboud University Medical Center, Nijmegen","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["Charcot-Marie-Tooth disease, type 4B1, 601382"],"mode_of_inheritance":"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."}]}},{"gene_data":{"alias":["KIAA1073"],"biotype":"protein_coding","hgnc_id":"HGNC:7450","gene_name":"myotubularin related protein 2","omim_gene":["603557"],"alias_name":["phosphatidylinositol-3-phosphatase","phosphoinositide-3-phosphatase"],"gene_symbol":"MTMR2","hgnc_symbol":"MTMR2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:95566046-95658479","ensembl_id":"ENSG00000087053"}},"GRch38":{"90":{"location":"11:95832882-95925315","ensembl_id":"ENSG00000087053"}}},"hgnc_date_symbol_changed":"1999-02-05"},"entity_type":"gene","entity_name":"MTMR2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert Review Amber","BRIDGE study SPEED NEURO Tier1 Gene"],"phenotypes":["Charcot-Marie-Tooth disease, type 4B, 601382"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}