tricuspid valve stenosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A tricuspid valve disease that is characterized by the narrowing of the orifice of the tricuspid valve of the heart. This causes increased resistance to blood flow through the valve. (Human Disease Ontology, DOID_4078)
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11 genes co-occuring with the disease tricuspid valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HEY2 hes-related family bHLH transcription factor with YRPW motif 2 1.57913
SNAPIN SNAP-associated protein 1.56844
SLC6A11 solute carrier family 6 (neurotransmitter transporter), member 11 1.37861
OXTR oxytocin receptor 1.02524
JAG1 jagged 1 0.765127
NOTCH1 notch 1 0.713198
CD59 CD59 molecule, complement regulatory protein 0.685491
FLNA filamin A, alpha 0.664372
GJA1 gap junction protein, alpha 1, 43kDa 0.565666
HBA2 hemoglobin, alpha 2 0.249608
SST somatostatin 0.185313