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Symbol Name ID |
Rad51
RAD51 recombinase MGI:97890 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chromosomal breakage induced by crosslinking agents |
| Disease(s) Associated with RAD51 | |
| Fanconi anemia complementation group R |
| Mouse Phenotypes | abnormal spermatocyte morphology |
abnormal spermatogonia morphology |
decreased male germ cell number |
abnormal male meiosis |
increased cellular sensitivity to gamma-irradiation |
increased embryonic epiblast cell apoptosis |
increased male germ cell apoptosis |
absent inner cell mass proliferation |
decreased cell proliferation |
abnormal double-strand DNA break repair |
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| Availability | Mouse Genotype | ||||||||||
| Rad51tm1Hst/Rad51tm1Hst | |||||||||||
| Rad51tm1Csha/Rad51tm1Csha Tg(Ddx4-cre)1Dcas/0 (conditional) |
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| Rad51tm1Csha/Rad51tm1Csha Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ (conditional) |
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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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