{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DISPA","MGC13130","DKFZP434I0428","MGC16796"],"biotype":"protein_coding","hgnc_id":"HGNC:19711","gene_name":"dispatched RND transporter family member 1","omim_gene":["607502"],"alias_name":null,"gene_symbol":"DISP1","hgnc_symbol":"DISP1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:222988406-223179337","ensembl_id":"ENSG00000154309"}},"GRch38":{"90":{"location":"1:222872271-223005995","ensembl_id":"ENSG00000154309"}}},"hgnc_date_symbol_changed":"2003-12-12"},"entity_type":"gene","entity_name":"DISP1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Craniofacial and neuro-developmental abnormalities (Roessler (2009) Hum Genet125,393)","Diaphragmatic hernia, congenital (Kantarci (2010) Am J Med Genet A 152A,2493)","Tetralogy of Fallot (Silversides (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"}]}},{"gene_data":{"alias":["DISPA","MGC13130","DKFZP434I0428","MGC16796"],"biotype":"protein_coding","hgnc_id":"HGNC:19711","gene_name":"dispatched RND transporter family member 1","omim_gene":["607502"],"alias_name":null,"gene_symbol":"DISP1","hgnc_symbol":"DISP1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:222988406-223179337","ensembl_id":"ENSG00000154309"}},"GRch38":{"90":{"location":"1:222872271-223005995","ensembl_id":"ENSG00000154309"}}},"hgnc_date_symbol_changed":"2003-12-12"},"entity_type":"gene","entity_name":"DISP1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27363716"],"evidence":["NHS GMS","Expert Review Green","Expert list"],"phenotypes":["Holoprosencephaly"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":78,"hash_id":"568e87e022c1fc1c79ca1754","name":"Holoprosencephaly","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"1.23","version_created":"2019-09-30T12:37:25.593251Z","relevant_disorders":["Rhombencephalosynapsis","Holoprosencephaly - NOT chromosomal; R85"],"stats":{"number_of_genes":18,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}