malignant ependymoma Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A malignant glioma that is derived from ependymal cells, a type of glial cell, located_in ventricle lining within the central part of the brain. (Human Disease Ontology, DOID_5074)
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Genes

59 genes co-occuring with the disease malignant ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
EPB41L2 erythrocyte membrane protein band 4.1-like 2 1.28872
NF2 neurofibromin 2 (merlin) 1.27344
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome 1.04209
BCAT1 branched chain amino-acid transaminase 1, cytosolic 1.00921
AES amino-terminal enhancer of split 1.00414
CBX7 chromobox homolog 7 0.985164
CLDN6 claudin 6 0.888848
GNB1L guanine nucleotide binding protein (G protein), beta polypeptide 1-like 0.867959
SOX6 SRY (sex determining region Y)-box 6 0.856497
EPB41 erythrocyte membrane protein band 4.1 0.856087
SOX11 SRY (sex determining region Y)-box 11 0.681894
PDGFA platelet-derived growth factor alpha polypeptide 0.678701
HEY2 hes-related family bHLH transcription factor with YRPW motif 2 0.65763
SOX4 SRY (sex determining region Y)-box 4 0.638676
EPHB2 EPH receptor B2 0.578883
SYP synaptophysin 0.566443
TGFB2 transforming growth factor, beta 2 0.554791
FANCL Fanconi anemia, complementation group L 0.551686
HMOX2 heme oxygenase 2 0.529222
FAM195A family with sequence similarity 195, member A 0.526518
TNC tenascin C 0.520346
FBXW7 F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase 0.514186
GCLC glutamate-cysteine ligase, catalytic subunit 0.489311
ROS1 ROS proto-oncogene 1 , receptor tyrosine kinase 0.482844
TERT telomerase reverse transcriptase 0.467306
E2F1 E2F transcription factor 1 0.464283
AQP1 aquaporin 1 (Colton blood group) 0.460506
TP53 tumor protein p53 0.457487
NOTCH1 notch 1 0.456355
ATRX alpha thalassemia/mental retardation syndrome X-linked 0.44129
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 0.424765
WNT5A wingless-type MMTV integration site family, member 5A 0.409414
PRDX5 peroxiredoxin 5 0.395608
ANXA1 annexin A1 0.389653
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7 0.355235
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase 0.353763
TGFB3 transforming growth factor, beta 3 0.344574
EGFR epidermal growth factor receptor 0.336144
SOX9 SRY (sex determining region Y)-box 9 0.294413
LGALS1 lectin, galactoside-binding, soluble, 1 0.284371
RBFOX3 RNA binding protein, fox-1 homolog (C. elegans) 3 0.280439
GFAP glial fibrillary acidic protein 0.271886
ERBB4 erb-b2 receptor tyrosine kinase 4 0.261952
PTER phosphotriesterase related 0.246799
NKX2-1 NK2 homeobox 1 0.229024
CDKN2A cyclin-dependent kinase inhibitor 2A 0.218374
PTEN phosphatase and tensin homolog 0.218034
MAP2 microtubule-associated protein 2 0.207245
ERBB3 erb-b2 receptor tyrosine kinase 3 0.190786
EWSR1 EWS RNA-binding protein 1 0.18591
AKT1 v-akt murine thymoma viral oncogene homolog 1 0.175411
TXN thioredoxin 0.165217
MAPK3 mitogen-activated protein kinase 3 0.161331
NES nestin 0.160021
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha 0.144715
IGF1R insulin-like growth factor 1 receptor 0.143915
MEN1 multiple endocrine neoplasia I 0.143693
PROM1 prominin 1 0.143558
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 0.142234