tricuspid valve atresia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description congenital closure of the tricuspid valve (Mammalian Phenotype Ontology, MP_0006123)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006123
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Genes

7 gene mutations causing the tricuspid valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CC2D2A coiled-coil and C2 domain containing 2A
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
LEFTY1 left-right determination factor 1
LEFTY2 left-right determination factor 2
MMP21 matrix metallopeptidase 21
SMAD6 SMAD family member 6
ZFPM2 zinc finger protein, FOG family member 2