{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["coll-2","Sema-Z2"],"biotype":"protein_coding","hgnc_id":"HGNC:10726","gene_name":"semaphorin 3D","omim_gene":["609907"],"alias_name":null,"gene_symbol":"SEMA3D","hgnc_symbol":"SEMA3D","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:84624869-84816171","ensembl_id":"ENSG00000153993"}},"GRch38":{"90":{"location":"7:84995553-85186855","ensembl_id":"ENSG00000153993"}}},"hgnc_date_symbol_changed":"1999-06-25"},"entity_type":"gene","entity_name":"SEMA3D","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23372769","25839327"],"evidence":["Expert Review Amber","Alder Hey - Erasmus MC"],"phenotypes":["susceptibility to Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist"],"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":["coll-2","Sema-Z2"],"biotype":"protein_coding","hgnc_id":"HGNC:10726","gene_name":"semaphorin 3D","omim_gene":["609907"],"alias_name":null,"gene_symbol":"SEMA3D","hgnc_symbol":"SEMA3D","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:84624869-84816171","ensembl_id":"ENSG00000153993"}},"GRch38":{"90":{"location":"7:84995553-85186855","ensembl_id":"ENSG00000153993"}}},"hgnc_date_symbol_changed":"1999-06-25"},"entity_type":"gene","entity_name":"SEMA3D","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["29095749","27876815"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["coll-2","Sema-Z2"],"biotype":"protein_coding","hgnc_id":"HGNC:10726","gene_name":"semaphorin 3D","omim_gene":["609907"],"alias_name":null,"gene_symbol":"SEMA3D","hgnc_symbol":"SEMA3D","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:84624869-84816171","ensembl_id":"ENSG00000153993"}},"GRch38":{"90":{"location":"7:84995553-85186855","ensembl_id":"ENSG00000153993"}}},"hgnc_date_symbol_changed":"1999-06-25"},"entity_type":"gene","entity_name":"SEMA3D","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["http://dx.doi.org/10.1371/journal.pgen.1002843"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Tetralogy of Fallot (Siversides (2012) PLoS Genet 8,e1002843)"],"mode_of_inheritance":"","tags":[],"panel":{"id":212,"hash_id":"583c128f8f62036f70db8d29","name":"Familial non syndromic congenital heart disease","disease_group":"Cardiovascular disorders","disease_sub_group":"Congenital heart disease","status":"public","version":"1.49","version_created":"2019-08-07T15:17:24.060112Z","relevant_disorders":["Fallots tetralogy","Hypoplastic Left Heart Syndrome","Left Ventricular Outflow Tract obstruction disorders","Pulmonary atresia","Transposition of the great vessels","Familial non-syndromic congenital heart disease","Familial congenital heart disease","Congenital heart disease","Syndromic congenital heart disease","Isomerism and laterality disorders"],"stats":{"number_of_genes":47,"number_of_strs":0,"number_of_regions":8},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}