{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TRKC"],"biotype":"protein_coding","hgnc_id":"HGNC:8033","gene_name":"neurotrophic receptor tyrosine kinase 3","omim_gene":["191316"],"alias_name":null,"gene_symbol":"NTRK3","hgnc_symbol":"NTRK3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"15:88418230-88799999","ensembl_id":"ENSG00000140538"}},"GRch38":{"90":{"location":"15:87859751-88256768","ensembl_id":"ENSG00000140538"}}},"hgnc_date_symbol_changed":"1991-07-18"},"entity_type":"gene","entity_name":"NTRK3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["19040714","19556619"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["monogenic-polygenic"],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["TRKC"],"biotype":"protein_coding","hgnc_id":"HGNC:8033","gene_name":"neurotrophic receptor tyrosine kinase 3","omim_gene":["191316"],"alias_name":null,"gene_symbol":"NTRK3","hgnc_symbol":"NTRK3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"15:88418230-88799999","ensembl_id":"ENSG00000140538"}},"GRch38":{"90":{"location":"15:87859751-88256768","ensembl_id":"ENSG00000140538"}}},"hgnc_date_symbol_changed":"1991-07-18"},"entity_type":"gene","entity_name":"NTRK3","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}},{"gene_data":{"alias":["TRKC"],"biotype":"protein_coding","hgnc_id":"HGNC:8033","gene_name":"neurotrophic receptor tyrosine kinase 3","omim_gene":["191316"],"alias_name":null,"gene_symbol":"NTRK3","hgnc_symbol":"NTRK3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"15:88418230-88799999","ensembl_id":"ENSG00000140538"}},"GRch38":{"90":{"location":"15:87859751-88256768","ensembl_id":"ENSG00000140538"}}},"hgnc_date_symbol_changed":"1991-07-18"},"entity_type":"gene","entity_name":"NTRK3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":126,"hash_id":"558ac48fbb5a16630dcfeaad","name":"Hearing loss","disease_group":"Hearing and ear disorders","disease_sub_group":"Non-syndromic hearing loss","status":"public","version":"2.2","version_created":"2019-09-03T14:01:56.987667Z","relevant_disorders":["Congenital hearing impairment","Autosomal dominant deafness","Congenital hearing impairment (profound/severe)","R67"],"stats":{"number_of_genes":358,"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 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":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."},{"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)"}]}}]}
