urinary bladder sphincter dysfunction Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Abnormal function of a sphincter of the urinary bladder. (Human Phenotype Ontology, HP_0002839)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002839
Similar Terms
Downloads & Tools

Genes

16 genes associated with the urinary bladder sphincter dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ABCD1	ATP-binding cassette, sub-family D (ALD), member 1
ATL1	atlastin GTPase 1
ATXN1	ataxin 1
ATXN2	ataxin 2
ATXN3	ataxin 3
HSPD1	heat shock 60kDa protein 1 (chaperonin)
KIAA0196	KIAA0196
KIF1A	kinesin family member 1A
KIF5A	kinesin family member 5A
NIPA1	non imprinted in Prader-Willi/Angelman syndrome 1
REEP2	receptor accessory protein 2
RTN2	reticulon 2
SPAST	spastin
SPG11	spastic paraplegia 11 (autosomal recessive)
SPG7	spastic paraplegia 7 (pure and complicated autosomal recessive)
ZFYVE26	zinc finger, FYVE domain containing 26