ureteral duplication Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A developmental anomaly characterized by the presence of two, instead of one, ureter connecting a kidney to the bladder. (Human Phenotype Ontology, HP_0000073)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000073
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Genes

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

Symbol	Name
AXIN1	axin 1
B3GALTL	beta 1,3-galactosyltransferase-like
CPT2	carnitine palmitoyltransferase 2
FANCA	Fanconi anemia, complementation group A
FANCC	Fanconi anemia, complementation group C
FANCD2	Fanconi anemia, complementation group D2
FANCE	Fanconi anemia, complementation group E
GATA6	GATA binding protein 6
LMNA	lamin A/C
PIGA	phosphatidylinositol glycan anchor biosynthesis, class A
PIGL	phosphatidylinositol glycan anchor biosynthesis, class L
PORCN	porcupine homolog (Drosophila)
TNXB	tenascin XB
TP63	tumor protein p63
ZMPSTE24	zinc metallopeptidase STE24