heart left ventricle outflow tract stenosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal constriction or narrowing of the portion of the left ventricle through which blood normally flows into the aorta (Mammalian Phenotype Ontology, MP_0010448)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010448
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Genes

12 gene mutations causing the heart left ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACKR3 atypical chemokine receptor 3
ADAM19 ADAM metallopeptidase domain 19
HBEGF heparin-binding EGF-like growth factor
HOXA3 homeobox A3
INVS inversin
KLF3 Kruppel-like factor 3 (basic)
MUS81 MUS81 structure-specific endonuclease subunit
NKX2-5 NK2 homeobox 5
PHC1 polyhomeotic homolog 1 (Drosophila)
PLCE1 phospholipase C, epsilon 1
SOS1 son of sevenless homolog 1 (Drosophila)
WRN Werner syndrome, RecQ helicase-like