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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 | 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 04/16/2024 MGI 6.23 |
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