double outlet right ventricle with atrioventricular septal defect Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a form of DORV in which there is also a complete atrioventricular canal (Mammalian Phenotype Ontology, MP_0011667)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011667
Similar Terms
Downloads & Tools

Genes

11 gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS6 ADAM metallopeptidase with thrombospondin type 1 motif, 6
AP2B1 adaptor-related protein complex 2, beta 1 subunit
CC2D2A coiled-coil and C2 domain containing 2A
CCDC39 coiled-coil domain containing 39
DNAH5 dynein, axonemal, heavy chain 5
DYX1C1 dyslexia susceptibility 1 candidate 1
IFT27 intraflagellar transport 27
IFT74 intraflagellar transport 74
MYH10 myosin, heavy chain 10, non-muscle
PCSK5 proprotein convertase subtilisin/kexin type 5
PITX2 paired-like homeodomain 2