prolonged pr interval Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Increased time for the PR interval (beginning of the P wave to the beginning of the QRS complex). (Human Phenotype Ontology, HP_0012248)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0012248
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Genes

16 genes associated with the prolonged pr interval phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
SCN10A sodium channel, voltage gated, type X alpha subunit 2.8278
SCN5A sodium channel, voltage gated, type V alpha subunit 2.48731
CAV1 caveolin 1, caveolae protein, 22kDa 2.17537
ARHGAP24 Rho GTPase activating protein 24 1.94622
TBX5 T-box 5 1.93708
MEIS1 Meis homeobox 1 1.51005
ITGA9 integrin, alpha 9 1.46277
WNT11 wingless-type MMTV integration site family, member 11 1.19958
NKX2-5 NK2 homeobox 5 1.02042
SAMD3 sterile alpha motif domain containing 3 1.00059
MICAL2 microtubule associated monooxygenase, calponin and LIM domain containing 2 1.00059
MYO3A myosin IIIA 0.942765
VWC2L von Willebrand factor C domain containing protein 2-like 0.919744
BCL6 B-cell CLL/lymphoma 6 0.899912
MAGI1 membrane associated guanylate kinase, WW and PDZ domain containing 1 0.868241
MFSD2A major facilitator superfamily domain containing 2A 0.855449