{"count":4,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0473","PARK19"],"biotype":"protein_coding","hgnc_id":"HGNC:15469","gene_name":"DnaJ heat shock protein family (Hsp40) member C6","omim_gene":["608375"],"alias_name":["auxilin"],"gene_symbol":"DNAJC6","hgnc_symbol":"DNAJC6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:65713902-65881552","ensembl_id":"ENSG00000116675"}},"GRch38":{"90":{"location":"1:65248219-65415869","ensembl_id":"ENSG00000116675"}}},"hgnc_date_symbol_changed":"2001-03-30"},"entity_type":"gene","entity_name":"DNAJC6","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26528954","27687717","26703368","22563501","23211418"],"evidence":["Expert Review Green","Radboud University Medical Center, Nijmegen"],"phenotypes":["Parkinson disease 19, juvenile-onset, 615528","Parkinson disease 19a, juvenile-onset","Parkinson disease 19b, early-onset"],"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":["KIAA0473","PARK19"],"biotype":"protein_coding","hgnc_id":"HGNC:15469","gene_name":"DnaJ heat shock protein family (Hsp40) member C6","omim_gene":["608375"],"alias_name":["auxilin"],"gene_symbol":"DNAJC6","hgnc_symbol":"DNAJC6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:65713902-65881552","ensembl_id":"ENSG00000116675"}},"GRch38":{"90":{"location":"1:65248219-65415869","ensembl_id":"ENSG00000116675"}}},"hgnc_date_symbol_changed":"2001-03-30"},"entity_type":"gene","entity_name":"DNAJC6","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["23211418","27687717","26528954","22563501","26703368"],"evidence":["Wessex and West Midlands GLH","Yorkshire and North East GLH","NHS GMS","London North GLH","Expert Review Green"],"phenotypes":["Parkinson disease 19b, early-onset","Parkinson disease 19, juvenile-onset, 615528","Parkinson disease 19a, juvenile-onset"],"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":["KIAA0473","PARK19"],"biotype":"protein_coding","hgnc_id":"HGNC:15469","gene_name":"DnaJ heat shock protein family (Hsp40) member C6","omim_gene":["608375"],"alias_name":["auxilin"],"gene_symbol":"DNAJC6","hgnc_symbol":"DNAJC6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:65713902-65881552","ensembl_id":"ENSG00000116675"}},"GRch38":{"90":{"location":"1:65248219-65415869","ensembl_id":"ENSG00000116675"}}},"hgnc_date_symbol_changed":"2001-03-30"},"entity_type":"gene","entity_name":"DNAJC6","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Amber","Victorian Clinical Genetics Services"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":402,"hash_id":null,"name":"Genetic epilepsy syndromes","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Inherited Epilepsy Syndromes","status":"public","version":"1.363","version_created":"2019-10-08T10:06:11.607307Z","relevant_disorders":["Epilepsy Plus","Epilepsy plus other features","Genetic Epilepsy Syndromes","Epileptic encephalopathy","Familial Focal Epilepsies","Familial Genetic Generalised Epilepsies","Genetic Epilepsies with Febrile Seizures Plus (GEFS+)","Genetic Epilepsies with Febrile Seizures Plus"],"stats":{"number_of_genes":614,"number_of_strs":2,"number_of_regions":13},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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":["KIAA0473","PARK19"],"biotype":"protein_coding","hgnc_id":"HGNC:15469","gene_name":"DnaJ heat shock protein family (Hsp40) member C6","omim_gene":["608375"],"alias_name":["auxilin"],"gene_symbol":"DNAJC6","hgnc_symbol":"DNAJC6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:65713902-65881552","ensembl_id":"ENSG00000116675"}},"GRch38":{"90":{"location":"1:65248219-65415869","ensembl_id":"ENSG00000116675"}}},"hgnc_date_symbol_changed":"2001-03-30"},"entity_type":"gene","entity_name":"DNAJC6","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["26528954","23211418","27687717","26703368","22563501"],"evidence":["NHS GMS","London North GLH","Expert Review Green"],"phenotypes":["Parkinson disease 19a, juvenile-onset","Parkinson disease 19, juvenile-onset, 615528","Parkinson disease 19b, early-onset"],"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)"}]}}]}