urinary urgency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Urge incontinence is the strong, sudden need to urinate. (Human Phenotype Ontology, HP_0000012)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000012
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Genes

18 genes associated with the urinary urgency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL1 atlastin GTPase 1
ATXN10 ataxin 10
B4GALNT1 beta-1,4-N-acetyl-galactosaminyl transferase 1
FA2H fatty acid 2-hydroxylase
HSPD1 heat shock 60kDa protein 1 (chaperonin)
KIAA0196 KIAA0196
KIF5A kinesin family member 5A
MARS2 methionyl-tRNA synthetase 2, mitochondrial
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
PINK1 PTEN induced putative kinase 1
REEP1 receptor accessory protein 1
RTN2 reticulon 2
SACS sacsin molecular chaperone
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TRPV4 transient receptor potential cation channel, subfamily V, member 4
ZFYVE26 zinc finger, FYVE domain containing 26