intraocular retinoblastoma Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A retinoblastoma that is located_in the eye and has not spread to other parts of the body. (Human Disease Ontology, DOID_4653)
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Genes

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

Symbol Name Standardized Value
RB1 retinoblastoma 1 1.31799
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2 1.04672
PIDD1 p53-induced death domain protein 1 0.988535
GREM2 gremlin 2, DAN family BMP antagonist 0.950769
ASS1 argininosuccinate synthase 1 0.866321
PVALB parvalbumin 0.646559
MLX MLX, MAX dimerization protein 0.626888
BPIFA1 BPI fold containing family A, member 1 0.581606
MMD monocyte to macrophage differentiation-associated 0.513802
DHFR dihydrofolate reductase 0.512264
LCK LCK proto-oncogene, Src family tyrosine kinase 0.458241
ENO2 enolase 2 (gamma, neuronal) 0.35082
SYP synaptophysin 0.304142
CRX cone-rod homeobox 0.25207