{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MTMR5","DENND7A"],"biotype":"protein_coding","hgnc_id":"HGNC:10542","gene_name":"SET binding factor 1","omim_gene":["603560"],"alias_name":["myotubularin related 5","DENN/MADD domain containing 7A"],"gene_symbol":"SBF1","hgnc_symbol":"SBF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:50883429-50913454","ensembl_id":"ENSG00000100241"}},"GRch38":{"90":{"location":"22:50445000-50475024","ensembl_id":"ENSG00000100241"}}},"hgnc_date_symbol_changed":"1998-07-28"},"entity_type":"gene","entity_name":"SBF1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}},{"gene_data":{"alias":["MTMR5","DENND7A"],"biotype":"protein_coding","hgnc_id":"HGNC:10542","gene_name":"SET binding factor 1","omim_gene":["603560"],"alias_name":["myotubularin related 5","DENN/MADD domain containing 7A"],"gene_symbol":"SBF1","hgnc_symbol":"SBF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:50883429-50913454","ensembl_id":"ENSG00000100241"}},"GRch38":{"90":{"location":"22:50445000-50475024","ensembl_id":"ENSG00000100241"}}},"hgnc_date_symbol_changed":"1998-07-28"},"entity_type":"gene","entity_name":"SBF1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28005197","23749797","21210780","24799518"],"evidence":["South West GLH","NHS GMS","London North GLH","Expert Review Red","Expert Review"],"phenotypes":["Charcot-Marie-Tooth disease, type 4B3, 615284"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["watchlist"],"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."}]}}]}
