Symbol Name ID |
Clxn
calaxin MGI:1914043 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Ectopic pregnancy |
Abnormal sperm motility |
Female infertility |
Male infertility |
Disease(s) Associated with CLXN | ||||
primary ciliary dyskinesia |
Mouse Phenotypes | reproductive system phenotype |
asthenozoospermia |
decreased litter size |
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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 08/02/2024 MGI 6.24 |
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