Symbol Name ID |
Clxn
calaxin MGI:1914043 |
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 |
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Availability | Mouse Genotype | ||||
Clxntm1.1Osb/Clxntm1.1Osb |
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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last database update 04/16/2024 MGI 6.23 |
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