intraventricular block Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absent or delayed conduction within the ventricular conducting system or in the ventricular myocardium (Mammalian Phenotype Ontology, MP_0010560)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010560
Similar Terms
Downloads & Tools

Genes

20 gene mutations causing the intraventricular block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DMD dystrophin
ESRRG estrogen-related receptor gamma
GJA1 gap junction protein, alpha 1, 43kDa
GJA5 gap junction protein, alpha 5, 40kDa
HOPX HOP homeobox
IDUA iduronidase, alpha-L-
IRX3 iroquois homeobox 3
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LMNA lamin A/C
MYLK3 myosin light chain kinase 3
NKX2-5 NK2 homeobox 5
PITX2 paired-like homeodomain 2
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SYNE1 spectrin repeat containing, nuclear envelope 1
TBX3 T-box 3
TBX5 T-box 5
THRA thyroid hormone receptor, alpha
VCL vinculin
VEGFA vascular endothelial growth factor A