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
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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