About   Help   FAQ
Symbol
Name
ID
Clxn
calaxin
MGI:1914043
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Morphological central nervous system abnormality
Hydrocephalus
Ventriculomegaly
Delayed speech and language development
Disease(s) Associated with CLXN
primary ciliary dyskinesia

Mouse Phenotypes
abnormal brain ependyma motile cilium physiology
hydrocephaly
enlarged brain ventricles
enlarged lateral ventricles
Availability Mouse Genotype
Clxntm1.1Osb/Clxntm1.1Osb

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory