congenital syphilis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A syphilis that results_in a multisystem infection in the fetus via the placenta. (Human Disease Ontology, DOID_9856)
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18 genes co-occuring with the disease congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
EXTL3 exostosin-like glycosyltransferase 3 2.56499
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 1.05429
PRSS21 protease, serine, 21 (testisin) 0.967083
TES testin LIM domain protein 0.885979
DCPS decapping enzyme, scavenger 0.873691
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13 0.783526
GALK1 galactokinase 1 0.747204
NCR3 natural cytotoxicity triggering receptor 3 0.655254
PRRC2A proline-rich coiled-coil 2A 0.644192
SLC25A16 solute carrier family 25 (mitochondrial carrier), member 16 0.629242
RRM1 ribonucleotide reductase M1 0.476772
WDFY2 WD repeat and FYVE domain containing 2 0.465794
CXCL13 chemokine (C-X-C motif) ligand 13 0.45447
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 0.433021
IRF6 interferon regulatory factor 6 0.385936
PER1 period circadian clock 1 0.277227
LCK LCK proto-oncogene, Src family tyrosine kinase 0.218374
G6PD glucose-6-phosphate dehydrogenase 0.172291