embryonal renal neoplasm Gene Set

Dataset HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0011794
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Genes

21 genes associated with the embryonal renal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
BRCA2 breast cancer 2, early onset
BUB1 BUB1 mitotic checkpoint serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
BUB3 BUB3 mitotic checkpoint protein
CDC73 cell division cycle 73
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEP57 centrosomal protein 57kDa
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
GPC3 glypican 3
GPC4 glypican 4
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HDAC4 histone deacetylase 4
IGF2 insulin-like growth factor 2
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
NSD1 nuclear receptor binding SET domain protein 1
PALB2 partner and localizer of BRCA2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
TP53 tumor protein p53
TRIM37 tripartite motif containing 37
WT1 Wilms tumor 1