Primary Identifier | MGI:5696519 | Allele Type | Chemically induced (ENU) |
Gene | Nat8f5 | Strain of Origin | C57BL/6J |
Is Recombinase | false | Is Wild Type | false |
Project Collection | B2B/CvDC |
description | Summative Diagnosis: Cardiovascular phenotypes: Congenital heart disease associated with with heterotaxy, including dextrocardia, double outlet right ventricle (DORV), Taussig-Bing type DORV, muscular VSD (mVSD), atrioventricular septal defects (AVSD), and coronary fistula Noncardiovascular phenotype: Dextrogastria, right lung isomerism, omphalocele, gastroschisis Phenotypic Similarity to Human Syndrome: Heterotaxy |