abnormal pr interval Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the length of time between the beginning of atrial depolarization and the beginning of ventricular depolarization, measured by the interval from the beginning of the P wave to the beginning of the QRS complex (Mammalian Phenotype Ontology, MP_0003901)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003901
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Genes

22 gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
DMPK dystrophia myotonica-protein kinase
EGFR epidermal growth factor receptor
EMD emerin
EPHA3 EPH receptor A3
EYA3 EYA transcriptional coactivator and phosphatase 3
GJA1 gap junction protein, alpha 1, 43kDa
GJA5 gap junction protein, alpha 5, 40kDa
GJD3 gap junction protein, delta 3, 31.9kDa
HADHB hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
IGHMBP2 immunoglobulin mu binding protein 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KEL Kell blood group, metallo-endopeptidase
LMNA lamin A/C
MIR208A microRNA 208a
MMP7 matrix metallopeptidase 7
NKX2-5 NK2 homeobox 5
SCN5A sodium channel, voltage gated, type V alpha subunit
SYNE1 spectrin repeat containing, nuclear envelope 1
TBX3 T-box 3
TBX5 T-box 5
VEGFB vascular endothelial growth factor B
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