abnormal sinoatrial node conduction Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the generation or transfer of electrical impulses that trigger contraction of the atria and ventricles (Mammalian Phenotype Ontology, MP_0006142)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006142
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28 gene mutations causing the abnormal sinoatrial node conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKAP10 A kinase (PRKA) anchor protein 10
ANK2 ankyrin 2, neuronal
BVES blood vessel epicardial substance
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CAMK2D calcium/calmodulin-dependent protein kinase II delta
DMD dystrophin
GJA1 gap junction protein, alpha 1, 43kDa
GJA5 gap junction protein, alpha 5, 40kDa
GNB5 guanine nucleotide binding protein (G protein), beta 5
HCN2 hyperpolarization activated cyclic nucleotide gated potassium channel 2
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
HOPX HOP homeobox
IDUA iduronidase, alpha-L-
IGHMBP2 immunoglobulin mu binding protein 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KL klotho
LMNA lamin A/C
MIR208A microRNA 208a
MMP7 matrix metallopeptidase 7
NUP155 nucleoporin 155kDa
POPDC2 popeye domain containing 2
RGS6 regulator of G-protein signaling 6
SCN5A sodium channel, voltage gated, type V alpha subunit
SLC2A8 solute carrier family 2 (facilitated glucose transporter), member 8
SP4 Sp4 transcription factor
TBX3 T-box 3
TBX5 T-box 5