{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CDHN","CD325"],"biotype":"protein_coding","hgnc_id":"HGNC:1759","gene_name":"cadherin 2","omim_gene":["114020"],"alias_name":["N-cadherin"],"gene_symbol":"CDH2","hgnc_symbol":"CDH2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"18:25530930-25757410","ensembl_id":"ENSG00000170558"}},"GRch38":{"90":{"location":"18:27950966-28177446","ensembl_id":"ENSG00000170558"}}},"hgnc_date_symbol_changed":"1991-09-13"},"entity_type":"gene","entity_name":"CDH2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["28326674","28280076","24294380"],"evidence":["Expert Review Amber","Expert list"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":134,"hash_id":"55a3876e22c1fc63fec6d0da","name":"Arrhythmogenic cardiomyopathy","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.41","version_created":"2019-10-03T13:27:28.690231Z","relevant_disorders":["Arrhythmogenic Right Ventricular Cardiomyopathy","Arrythmogenic cardiomyopathy","R133"],"stats":{"number_of_genes":19,"number_of_strs":0,"number_of_regions":0},"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)"}]}},{"gene_data":{"alias":["CDHN","CD325"],"biotype":"protein_coding","hgnc_id":"HGNC:1759","gene_name":"cadherin 2","omim_gene":["114020"],"alias_name":["N-cadherin"],"gene_symbol":"CDH2","hgnc_symbol":"CDH2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"18:25530930-25757410","ensembl_id":"ENSG00000170558"}},"GRch38":{"90":{"location":"18:27950966-28177446","ensembl_id":"ENSG00000170558"}}},"hgnc_date_symbol_changed":"1991-09-13"},"entity_type":"gene","entity_name":"CDH2","confidence_level":"0","penetrance":"unknown","mode_of_pathogenicity":null,"publications":["31585109","9015265","17222817"],"evidence":["Literature"],"phenotypes":["Abnormality of the corpus callosum","Abnormality of neuronal migration","Bimanual synkinesia","Duane anomaly","Abnormality of cardiovascular system","Abnormality of the eye","Abnormality of the genital system","Global developmental delay","Intellectual disability"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}