venous insufficiency Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A vein disease that is characterized by impaired flow of blood through the veins. (Human Disease Ontology, DOID_10128)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0005293
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Genes

17 genes associated with the venous insufficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
GPR176 G protein-coupled receptor 176 2.22807
AGBL3 ATP/GTP binding protein-like 3 2.17907
CAMK4 calcium/calmodulin-dependent protein kinase IV 2.06104
CYP27C1 cytochrome P450, family 27, subfamily C, polypeptide 1 2.04588
SEMA3C sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C 1.96955
SCAPER S-phase cyclin A-associated protein in the ER 1.93483
ARHGAP24 Rho GTPase activating protein 24 1.92526
LTA4H leukotriene A4 hydrolase 1.92392
NKAIN2 Na+/K+ transporting ATPase interacting 2 1.9032
OSBPL3 oxysterol binding protein-like 3 1.83714
EBF1 early B-cell factor 1 1.8186
IRS1 insulin receptor substrate 1 1.74723
PBX1 pre-B-cell leukemia homeobox 1 0.840142
GADL1 glutamate decarboxylase-like 1 0.760868
BFSP2 beaded filament structural protein 2, phakinin 0.754273
ERC2 ELKS/RAB6-interacting/CAST family member 2 0.641745
NPAS3 neuronal PAS domain protein 3 0.589794