bundle branch block Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Block of conduction of electrical impulses along the Bundle of His or along one of its bundle branches. (Human Phenotype Ontology, HP_0011710)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010636
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Genes

20 gene mutations causing the bundle branch 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