urinary incontinence Gene Set

Dataset	MPO Gene-Phenotype 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://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003280
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Genes

7 gene mutations causing the urinary incontinence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CHRNA3	cholinergic receptor, nicotinic, alpha 3 (neuronal)
DST	dystonin
HTR3A	5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
KCNMA1	potassium channel, calcium activated large conductance subfamily M alpha, member 1
PI4K2A	phosphatidylinositol 4-kinase type 2 alpha
TAC1	tachykinin, precursor 1
TRPV4	transient receptor potential cation channel, subfamily V, member 4