renal duplication Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital anomaly of the urinary tract, in which the kidney is duplicated and is drained via two separate renal pelves and ureters. (Human Phenotype Ontology, HP_0000075)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000075
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Genes

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

Symbol Name
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CLIP2 CAP-GLY domain containing linker protein 2
ELN elastin
FOXC2 forkhead box C2
GPC3 glypican 3
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
LIMK1 LIM domain kinase 1
RFC2 replication factor C (activator 1) 2, 40kDa
ROR2 receptor tyrosine kinase-like orphan receptor 2
TBL2 transducin (beta)-like 2
WNT5A wingless-type MMTV integration site family, member 5A