{"count":6,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["26437029","27718516"],"evidence":["Expert Review Green","Other"],"phenotypes":["Short stature, brachydactyly, intellectual developmental disability, and seizures 617157","Pseudohypoparathyroidism-like disorder"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":null,"publications":[],"evidence":["NHS GMS","Expert Review Green","Other"],"phenotypes":["Short stature, brachydactyly, intellectual developmental disability, and seizures  617157"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["PAGE DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["Pseudohypoparathyroidism-like disorder"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"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":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["26437029"],"evidence":["DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["Pseudohypoparathyroidism-like disorder"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"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":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["26437029","27718516"],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Green","Expert Review"],"phenotypes":["Short stature, brachydactyly, intellectual developmental disability, and seizures 617157"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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":["FLJ10640","KIAA1933"],"biotype":"protein_coding","hgnc_id":"HGNC:25557","gene_name":"protein arginine methyltransferase 7","omim_gene":["610087"],"alias_name":null,"gene_symbol":"PRMT7","hgnc_symbol":"PRMT7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:68344877-68392466","ensembl_id":"ENSG00000132600"}},"GRch38":{"90":{"location":"16:68310974-68358563","ensembl_id":"ENSG00000132600"}}},"hgnc_date_symbol_changed":"2006-02-16"},"entity_type":"gene","entity_name":"PRMT7","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","Victorian Clinical Genetics Services","BRIDGE study SPEED NEURO Tier1 Gene"],"phenotypes":["Short stature, brachydactyly, intellectual developmental disability, and seizures\t617157"],"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"}]}}]}
