cerebellar medulloblastoma Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A cerebellum cancer that begins in the lower part of the brain on the floor of the skull. (Human Disease Ontology, DOID_0060104)
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Genes

24 genes co-occuring with the disease cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
DIS3L DIS3 like exosome 3'-5' exoribonuclease 1.6624
UBE2J1 ubiquitin-conjugating enzyme E2, J1 1.65475
ZFX zinc finger protein, X-linked 0.990644
BMP2K BMP2 inducible kinase 0.887208
APC adenomatous polyposis coli 0.850764
SETD1A SET domain containing 1A 0.769618
SYP synaptophysin 0.743141
ENO2 enolase 2 (gamma, neuronal) 0.72329
GNRHR gonadotropin-releasing hormone receptor 0.693499
SAG S-antigen; retina and pineal gland (arrestin) 0.60225
RBP3 retinol binding protein 3, interstitial 0.583163
TP53 tumor protein p53 0.446182
TPM1 tropomyosin 1 (alpha) 0.42739
NGFR nerve growth factor receptor 0.417644
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae) 0.40904
MAP2 microtubule-associated protein 2 0.34384
GFAP glial fibrillary acidic protein 0.331391
GGT2 gamma-glutamyltransferase 2 0.31464
NES nestin 0.313189
PTCH1 patched 1 0.298011
FGF1 fibroblast growth factor 1 (acidic) 0.240148
PROM1 prominin 1 0.214636
CRH corticotropin releasing hormone 0.205254
MB myoglobin 0.180367