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Symbol Name ID |
Fanci
Fanconi anemia, complementation group I MGI:2384790 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of chromosome stability |
Chromosomal breakage induced by crosslinking agents |
| Disease(s) Associated with FANCI | ||
| Fanconi anemia | ||
| Fanconi anemia complementation group I |
| Mouse Phenotypes | absent gametes |
azoospermia |
oligozoospermia |
decreased male germ cell number |
increased cellular sensitivity to DNA damaging agents |
increased male germ cell apoptosis |
early cellular replicative senescence |
abnormal DNA methylation during gametogenesis |
abnormal fibroblast physiology |
induced chromosome breakage |
spontaneous chromosome breakage |
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| Availability | Mouse Genotype | |||||||||||
| Fanciem2Szh/Fanciem2Szh | ||||||||||||
| Fancitm1.1Itl/Fancitm1.1Itl | ||||||||||||
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 04/30/2024 MGI 6.23 |
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