{"count":6,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","Expert","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen",""],"phenotypes":["Parkinson disease 15, autosomal recessive, 260300","Parkinson Disease, Recessive","Early Onset Complex Disease","parkinsonian-pyramidal syndrome"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":39,"hash_id":"58078e6e8f62030e233a8157","name":"Parkinson Disease and Complex Parkinsonism","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodegenerative disorders","status":"public","version":"1.66","version_created":"2019-06-20T15:15:15.111993Z","relevant_disorders":["Complex Parkinsonism (includes pallido-pyramidal syndromes)","Early onset and familial Parkinson's Disease"],"stats":{"number_of_genes":57,"number_of_strs":9,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","Emory Genetics Laboratory"],"phenotypes":["Dystonia","juvenile parkinsonism"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":192,"hash_id":"553f95c9bb5a1616e5ed45bf","name":"Early onset dystonia","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor Disorders of the CNS","status":"public","version":"1.81","version_created":"2019-09-23T11:22:14.418180Z","relevant_disorders":[],"stats":{"number_of_genes":111,"number_of_strs":4,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green"],"phenotypes":["Dystonia","juvenile parkinsonism"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":475,"hash_id":null,"name":"Dystonia - childhood onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.8","version_created":"2019-09-09T13:17:58.240159Z","relevant_disorders":[],"stats":{"number_of_genes":176,"number_of_strs":7,"number_of_regions":1},"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["18513678","19038853"],"evidence":["Wessex and West Midlands GLH","Yorkshire and North East GLH","NHS GMS","London North GLH","Expert Review Green"],"phenotypes":["Parkinson Disease, Recessive","Dystonia","juvenile parkinsonism","parkinsonian-pyramidal syndrome","Parkinson disease 15, autosomal recessive, 260300","Early Onset Complex Disease"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":474,"hash_id":null,"name":"Neurodegenerative disorders - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.106","version_created":"2019-09-20T16:19:10.101841Z","relevant_disorders":["R58"],"stats":{"number_of_genes":395,"number_of_strs":18,"number_of_regions":4},"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":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25085748"],"evidence":["Expert Review Red","BRIDGE study SPEED NEURO Tier1 Gene"],"phenotypes":["Parkinson disease 15, autosomal recessive  260300"],"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"}]}},{"gene_data":{"alias":["FBX7","Fbx","PARK15"],"biotype":"protein_coding","hgnc_id":"HGNC:13586","gene_name":"F-box protein 7","omim_gene":["605648"],"alias_name":null,"gene_symbol":"FBXO7","hgnc_symbol":"FBXO7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:32870663-32894818","ensembl_id":"ENSG00000100225"}},"GRch38":{"90":{"location":"22:32474676-32498829","ensembl_id":"ENSG00000100225"}}},"hgnc_date_symbol_changed":"2000-09-27"},"entity_type":"gene","entity_name":"FBXO7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","London North GLH","Expert Review Green"],"phenotypes":["Parkinson disease 15, autosomal recessive, 260300","Parkinson Disease, Recessive","Early Onset Complex Disease","juvenile parkinsonism","Dystonia","parkinsonian-pyramidal syndrome"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":540,"hash_id":null,"name":"Adult onset movement disorder","disease_group":"","disease_sub_group":"","status":"public","version":"0.125","version_created":"2019-09-29T14:25:05.513850Z","relevant_disorders":["R56"],"stats":{"number_of_genes":202,"number_of_strs":11,"number_of_regions":1},"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)"}]}}]}