hydroureter Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The distention of the ureter with urine. (Human Phenotype Ontology, HP_0000072)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000072
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Genes

11 genes associated with the hydroureter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHRM3 cholinergic receptor, muscarinic 3
FLNA filamin A, alpha
FOXF1 forkhead box F1
HPSE2 heparanase 2 (inactive)
MKKS McKusick-Kaufman syndrome
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
RAB23 RAB23, member RAS oncogene family
SETBP1 SET binding protein 1
SOX17 SRY (sex determining region Y)-box 17
TP63 tumor protein p63
WFS1 Wolfram syndrome 1 (wolframin)