bilateral retinoblastoma Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A retinoblastoma that develops in both eyes. (Human Disease Ontology, DOID_4650)
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Genes

23 genes co-occuring with the disease bilateral retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RB1 retinoblastoma 1 2.24098
DLG2 discs, large homolog 2 (Drosophila) 1.38428
ESD esterase D 1.2005
FGF3 fibroblast growth factor 3 0.698715
GREM2 gremlin 2, DAN family BMP antagonist 0.641433
FGFR3 fibroblast growth factor receptor 3 0.5645
CRYAA crystallin, alpha A 0.540442
TICAM2 toll-like receptor adaptor molecule 2 0.489691
COX5A cytochrome c oxidase subunit Va 0.463527
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 0.428891
RBP3 retinol binding protein 3, interstitial 0.422515
TP53 tumor protein p53 0.368888
SCN10A sodium channel, voltage gated, type X alpha subunit 0.362239
ARHGAP32 Rho GTPase activating protein 32 0.360026
NF1 neurofibromin 1 0.347879
MYOG myogenin (myogenic factor 4) 0.338341
ERAS ES cell expressed Ras 0.333218
KRT18 keratin 18, type I 0.318272
PIDD1 p53-induced death domain protein 1 0.312464
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.225917
SRY sex determining region Y 0.214975
FGFR2 fibroblast growth factor receptor 2 0.180084
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2 0.170544