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Symbol
Name
ID

Clcn1
chloride channel, voltage-sensitive 1
MGI:88417

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Dysphagia	Abnormality of the nervous system
Disease(s) Associated with CLCN1	Dysphagia	Abnormality of the nervous system
Becker disease

Mouse Phenotypes		axon degeneration	decreased prepulse inhibition
Availability	Mouse Genotype	axon degeneration	decreased prepulse inhibition
	Clcn1^adr-mto/Clcn1^adr-mto
	Clcn1^em1(IMPC)Mbp/Clcn1^em1(IMPC)Mbp

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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