embryonal renal neoplasm Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an embryonal neoplasm of the kidney that primarily affects children. (Human Phenotype Ontology, HP_0011794)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0011794
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Genes

5 genes associated with the embryonal renal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
DLG2 discs, large homolog 2 (Drosophila) 1.72215
TCN2 transcobalamin II 1.52822
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies) 1.35521
PCSK9 proprotein convertase subtilisin/kexin type 9 1.15352
DDX1 DEAD (Asp-Glu-Ala-Asp) box helicase 1 0.966449