glossopharyngeal nerve disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

19 genes co-occuring with the disease glossopharyngeal nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CRLF1 cytokine receptor-like factor 1 1.25602
TCEB2 transcription elongation factor B (SIII), polypeptide 2 (18kDa, elongin B) 1.16521
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3 1.13501
SRGN serglycin 1.09671
LONP1 lon peptidase 1, mitochondrial 1.01554
PTPRN2 protein tyrosine phosphatase, receptor type, N polypeptide 2 0.97338
MRPL49 mitochondrial ribosomal protein L49 0.921736
CANX calnexin 0.773705
MPO myeloperoxidase 0.651694
XPC xeroderma pigmentosum, complementation group C 0.588612
VIM vimentin 0.547807
HNF4A hepatocyte nuclear factor 4, alpha 0.430768
PRTN3 proteinase 3 0.395235
MMP3 matrix metallopeptidase 3 0.28831
ACE angiotensin I converting enzyme 0.227642
MBP myelin basic protein 0.215314
F5 coagulation factor V (proaccelerin, labile factor) 0.187719
SST somatostatin 0.137665
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic 0.134581