|
Symbol Name ID |
Ccin
calicin MGI:3045316 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Globozoospermia |
Irregularly shaped sperm tail |
Reduced progressive sperm motility |
Reduced sperm motility |
Oligozoospermia |
Male infertility |
| Disease(s) Associated with CCIN | ||||||
| spermatogenic failure 91 |
| Mouse Phenotypes | reproductive system phenotype |
oligozoospermia |
abnormal sperm head morphology |
abnormal acrosome morphology |
increased male germ cell apoptosis |
asthenozoospermia |
male infertility |
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| Availability | Mouse Genotype | |||||||
| Ccinem2Gpt/Ccinem2Gpt | * | |||||||
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 03/25/2025 MGI 6.24 |
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