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Symbol
Name
ID

Cldn11
claudin 11
MGI:106925

Phenotype annotations related to nervous system

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

Human Phenotypes	Drooling	CNS hypomyelination	Babinski sign	Delayed speech and language development	Dysarthria	Intellectual disability, borderline	Lower limb hyperreflexia	Inability to walk	Delayed ability to sit	Delayed ability to walk
Disease(s) Associated with CLDN11
hypomyelinating leukodystrophy 22

Mouse Phenotypes		nervous system phenotype	cochlear outer hair cell degeneration	abnormal myelin sheath morphology
Availability	Mouse Genotype
	Cldn11^tm1Ral/Cldn11^tm1Ral	*

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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