{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NRCAML","KIAA0756","FLJ46866","NF"],"biotype":"protein_coding","hgnc_id":"HGNC:29866","gene_name":"neurofascin","omim_gene":["609145"],"alias_name":null,"gene_symbol":"NFASC","hgnc_symbol":"NFASC","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:204797779-204991950","ensembl_id":"ENSG00000163531"}},"GRch38":{"90":{"location":"1:204828651-205022822","ensembl_id":"ENSG00000163531"}}},"hgnc_date_symbol_changed":"2005-11-22"},"entity_type":"gene","entity_name":"NFASC","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["28940097","30124836","30850329"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Neurodevelopmental disorder with central and peripheral motor dysfunction 618356"],"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"}]}}]}