paralytic squint Gene Set
Genes
8 genes co-occuring with the disease paralytic squint in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
| Symbol |
Name |
Standardized Value |
|
SSNA1
|
Sjogren syndrome nuclear autoantigen 1
|
1.64487
|
|
PHOX2A
|
paired-like homeobox 2a
|
1.43683
|
|
KIF21A
|
kinesin family member 21A
|
1.28042
|
|
FUT2
|
fucosyltransferase 2 (secretor status included)
|
0.956196
|
|
PPT1
|
palmitoyl-protein thioesterase 1
|
0.826178
|
|
CADM1
|
cell adhesion molecule 1
|
0.808949
|
|
PTCH1
|
patched 1
|
0.670732
|
|
PRL
|
prolactin
|
0.373328
|
