irregular astigmatism Gene Set

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

20 genes co-occuring with the disease irregular astigmatism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
VSX1 visual system homeobox 1 1.59296
NYX nyctalopin 1.38428
MATK megakaryocyte-associated tyrosine kinase 1.30226
DDT D-dopachrome tautomerase 1.25733
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6 1.09419
FBXO7 F-box protein 7 1.08999
DCLRE1C DNA cross-link repair 1C 1.06144
TGFBI transforming growth factor, beta-induced, 68kDa 1.03788
STAP2 signal transducing adaptor family member 2 1.03493
C5ORF38 chromosome 5 open reading frame 38 1.02819
IFITM2 interferon induced transmembrane protein 2 0.915551
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9 0.903621
NMT1 N-myristoyltransferase 1 0.856087
LCK LCK proto-oncogene, Src family tyrosine kinase 0.769618
HSPG2 heparan sulfate proteoglycan 2 0.660008
ZEB1 zinc finger E-box binding homeobox 1 0.643009
FLNA filamin A, alpha 0.529608
DPT dermatopontin 0.519575
CD59 CD59 molecule, complement regulatory protein 0.481705
CD68 CD68 molecule 0.164571