abnormality of the heart valves Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a Cardiac valve. (Human Phenotype Ontology, HP_0001654)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001654
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Genes

15 genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MAML3 mastermind-like 3 (Drosophila) 0.99234
LPA lipoprotein, Lp(a) 0.909907
SLC9A3R2 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2 0.513114
HLA-B major histocompatibility complex, class I, B 0.415666
PIEZO1 piezo-type mechanosensitive ion channel component 1 0.40969
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 0.40817
ZNF385D zinc finger protein 385D 0.406502
REXO4 REX4, RNA exonuclease 4 homolog (S. cerevisiae) 0.397531
MYLK myosin light chain kinase 0.368571
ZBTB16 zinc finger and BTB domain containing 16 0.364969
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.360105
AXIN1 axin 1 0.359059
PDIA2 protein disulfide isomerase family A, member 2 0.356183
CD44 CD44 molecule (Indian blood group) 0.34482
CSF1R colony stimulating factor 1 receptor 0.344529