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Symbol
Name
ID

Kcnu1
potassium channel, subfamily U, member 1
MGI:1202300

Phenotype annotations related to reproductive system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Coiled sperm flagella	Reduced sperm motility	Oligozoospermia	Male infertility
Disease(s) Associated with KCNU1
spermatogenic failure 79

Mouse Phenotypes		reproductive system phenotype	decreased sperm progressive motility	asthenozoospermia	impaired sperm capacitation	male infertility	impaired acrosome reaction	impaired fertilization	abnormal sperm physiology
Availability	Mouse Genotype	reproductive system phenotype	decreased sperm progressive motility	asthenozoospermia	impaired sperm capacitation	male infertility	impaired acrosome reaction	impaired fertilization	abnormal sperm physiology
	Kcnu1^tm1.1Clin/Kcnu1^tm1.1Clin	*
	Kcnu1^tm1.2Clin/Kcnu1^tm1.2Clin
	Kcnu1^tm1Cmsa/Kcnu1^tm1Cmsa
	Kcnu1^tm1.1Clin/Kcnu1⁺	*
	Kcnu1^tm1.2Clin/Kcnu1⁺	*

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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