urinary incontinence Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Loss of the ability to control the urinary bladder leading to involuntary urination. (Human Phenotype Ontology, HP_0000020)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000020
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Genes

44 genes associated with the urinary incontinence 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
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
AP5Z1 adaptor-related protein complex 5, zeta 1 subunit
ARSA arylsulfatase A
ATL1 atlastin GTPase 1
ATXN10 ataxin 10
AUH AU RNA binding protein/enoyl-CoA hydratase
CHMP2B charged multivesicular body protein 2B
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
DDHD2 DDHD domain containing 2
FA2H fatty acid 2-hydroxylase
FAM134B family with sequence similarity 134, member B
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
FMR1 fragile X mental retardation 1
FUZ fuzzy planar cell polarity protein
GBA2 glucosidase, beta (bile acid) 2
GJC2 gap junction protein, gamma 2, 47kDa
HEXB hexosaminidase B (beta polypeptide)
HMBS hydroxymethylbilane synthase
HSPD1 heat shock 60kDa protein 1 (chaperonin)
HTRA1 HtrA serine peptidase 1
IGHMBP2 immunoglobulin mu binding protein 2
KIAA0196 KIAA0196
KIF5A kinesin family member 5A
MNX1 motor neuron and pancreas homeobox 1
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
NOTCH3 notch 3
PANK2 pantothenate kinase 2
PSAP prosaposin
RTN2 reticulon 2
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TBP TATA box binding protein
TREM2 triggering receptor expressed on myeloid cells 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTR transthyretin
TYROBP TYRO protein tyrosine kinase binding protein
VANGL1 VANGL planar cell polarity protein 1
VANGL2 VANGL planar cell polarity protein 2
ZFYVE26 zinc finger, FYVE domain containing 26
ZNF592 zinc finger protein 592