{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:497","gene_name":"transient receptor potential cation channel subfamily A member 1","omim_gene":["604775"],"alias_name":null,"gene_symbol":"TRPA1","hgnc_symbol":"TRPA1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"8:72932152-72987852","ensembl_id":"ENSG00000104321"}},"GRch38":{"90":{"location":"8:72019917-72075617","ensembl_id":"ENSG00000104321"}}},"hgnc_date_symbol_changed":"2003-11-20"},"entity_type":"gene","entity_name":"TRPA1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["20547126","16564016","21468319","28314413","24778270","24564660","20718100","28436534"],"evidence":["Expert Review Green","Review","Literaure"],"phenotypes":["Episodic pain syndrome, familial,  615040","Familial episodic pain syndrome type I"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":288,"hash_id":"59621a1c8f62036f45d561a3","name":"Pain syndromes","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Channelopathies","status":"public","version":"1.8","version_created":"2019-10-08T10:46:35.875259Z","relevant_disorders":["neuropathic pain","Pain channelopathies"],"stats":{"number_of_genes":26,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:497","gene_name":"transient receptor potential cation channel subfamily A member 1","omim_gene":["604775"],"alias_name":null,"gene_symbol":"TRPA1","hgnc_symbol":"TRPA1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:72932152-72987852","ensembl_id":"ENSG00000104321"}},"GRch38":{"90":{"location":"8:72019917-72075617","ensembl_id":"ENSG00000104321"}}},"hgnc_date_symbol_changed":"2003-11-20"},"entity_type":"gene","entity_name":"TRPA1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["28314413","20718100","28436534","24778270","16564016","20547126","24564660","21468319"],"evidence":["Expert Review Red","NHS GMS","London North GLH","Wessex and West Midlands GLH"],"phenotypes":["?Episodic pain syndrome, familial, 1, 615040","Familial episodic pain syndrome type I"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":541,"hash_id":null,"name":"Paroxysmal central nervous system disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.168","version_created":"2019-10-01T13:39:46.962209Z","relevant_disorders":["Paroxysmal neurological disorders","pain disorders and sleep disorders"],"stats":{"number_of_genes":83,"number_of_strs":5,"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)"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:497","gene_name":"transient receptor potential cation channel subfamily A member 1","omim_gene":["604775"],"alias_name":null,"gene_symbol":"TRPA1","hgnc_symbol":"TRPA1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:72932152-72987852","ensembl_id":"ENSG00000104321"}},"GRch38":{"90":{"location":"8:72019917-72075617","ensembl_id":"ENSG00000104321"}}},"hgnc_date_symbol_changed":"2003-11-20"},"entity_type":"gene","entity_name":"TRPA1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","London North GLH"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"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."}]}}]}