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Symbol
Name
ID

Kcnk9
potassium channel, subfamily K, member 9
MGI:3521816

Phenotype annotations related to nervous system

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

Human Phenotypes	Dysphagia	Intellectual disability	Global developmental delay
Disease(s) Associated with KCNK9
Birk-Barel syndrome

Mouse Phenotypes		nervous system phenotype	abnormal action potential
Availability	Mouse Genotype	nervous system phenotype	abnormal action potential
	Kcnk9^tm1.1Daba/Kcnk9^tm1.1Daba	*
	Kcnk9^tm1.1Fles/Kcnk9^tm1.1Fles	*

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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