hypovolemia Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An decrease in the amount of intravascular fluid, particularly in the volume of the circulating blood. (Human Phenotype Ontology, HP_0011106)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0011106
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Genes

14 genes associated with the hypovolemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MICB MHC class I polypeptide-related sequence B 1.46277
PLCE1 phospholipase C, epsilon 1 1.40061
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1 1.12851
CCHCR1 coiled-coil alpha-helical rod protein 1 0.951856
COL9A3 collagen, type IX, alpha 3 0.823019
CPEB4 cytoplasmic polyadenylation element binding protein 4 0.819829
PIGN phosphatidylinositol glycan anchor biosynthesis, class N 0.789787
GRK6 G protein-coupled receptor kinase 6 0.742794
AKAP1 A kinase (PRKA) anchor protein 1 0.724474
GABRB1 gamma-aminobutyric acid (GABA) A receptor, beta 1 0.701779
DBN1 drebrin 1 0.683684
GPM6A glycoprotein M6A 0.667695
STK24 serine/threonine kinase 24 0.599613
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box) 0.580093