{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:9839","gene_name":"RAS like proto-oncogene A","omim_gene":["179550"],"alias_name":["RAS-like protein A","Ras-related protein Ral-A","Ras family small GTP binding protein RALA","ras related GTP binding protein A"],"gene_symbol":"RALA","hgnc_symbol":"RALA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:39663082-39747723","ensembl_id":"ENSG00000006451"}},"GRch38":{"90":{"location":"7:39623483-39708124","ensembl_id":"ENSG00000006451"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"RALA","confidence_level":"3","penetrance":"unknown","mode_of_pathogenicity":"Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","publications":["30500825"],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Green","Literature"],"phenotypes":["Global developmental delay","Intellectual disability","Seizures","Abnormality of nervous system morphology"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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":[],"biotype":"protein_coding","hgnc_id":"HGNC:9839","gene_name":"RAS like proto-oncogene A","omim_gene":["179550"],"alias_name":["RAS-like protein A","Ras-related protein Ral-A","Ras family small GTP binding protein RALA","ras related GTP binding protein A"],"gene_symbol":"RALA","hgnc_symbol":"RALA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:39663082-39747723","ensembl_id":"ENSG00000006451"}},"GRch38":{"90":{"location":"7:39623483-39708124","ensembl_id":"ENSG00000006451"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"RALA","confidence_level":"3","penetrance":"unknown","mode_of_pathogenicity":"Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","publications":["30500825"],"evidence":["Expert Review","Expert Review Green","Expert Review","Literature"],"phenotypes":["Global developmental delay","Seizures","Abnormality of nervous system morphology","Global developmental delay, Intellectual disability, Seizures, Abnormality of nervous system morphology","Intellectual disability"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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"}]}}]}