skull base meningioma 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 skull base meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FOXRED1 FAD-dependent oxidoreductase domain containing 1 1.53701
OTP orthopedia homeobox 1.53128
KRT84 keratin 84, type II 1.19921
SCRT1 scratch family zinc finger 1 1.13755
KRT83 keratin 83, type II 1.03451
SLC25A16 solute carrier family 25 (mitochondrial carrier), member 16 0.885569
RICTOR RPTOR independent companion of MTOR, complex 2 0.816334
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class) 0.754527
SSTR2 somatostatin receptor 2 0.749237
SST somatostatin 0.647743
MMD monocyte to macrophage differentiation-associated 0.538118
NF2 neurofibromin 2 (merlin) 0.424014
WT1 Wilms tumor 1 0.32774
NOTCH1 notch 1 0.223165
HLA-C major histocompatibility complex, class I, C 0.16933
VWF von Willebrand factor 0.141373
FN1 fibronectin 1 0.140948
FTL ferritin, light polypeptide 0.138425
FTH1 ferritin, heavy polypeptide 1 0.138425