central nervous system mesenchymal non-meningothelial tumor Gene Set

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

24 genes co-occuring with the disease central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MYOD1 myogenic differentiation 1 1.19186
CD99 CD99 molecule 1.18884
PAX3 paired box 3 1.09377
MYF6 myogenic factor 6 (herculin) 1.06186
PAX7 paired box 7 1.0442
CENPV centromere protein V 1.03282
ETV1 ets variant 1 0.861818
MYOG myogenin (myogenic factor 4) 0.847078
EWSR1 EWS RNA-binding protein 1 0.830279
MYF5 myogenic factor 5 0.815514
HMGA1 high mobility group AT-hook 1 0.678701
ETV6 ets variant 6 0.546644
WT1 Wilms tumor 1 0.525746
PIDD1 p53-induced death domain protein 1 0.474877
FUS FUS RNA binding protein 0.430393
HMGA2 high mobility group AT-hook 2 0.413527
CD34 CD34 molecule 0.401945
HBA1 hemoglobin, alpha 1 0.369997
HBA2 hemoglobin, alpha 2 0.348614
LCK LCK proto-oncogene, Src family tyrosine kinase 0.305587
NPY neuropeptide Y 0.278297
KRT20 keratin 20, type I 0.240148
KRT7 keratin 7, type II 0.186811
MB myoglobin 0.185313