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Symbol Name ID |
Rad51c
RAD51 paralog C MGI:2150020 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chromosome breakage |
| Disease(s) Associated with RAD51C | |
| Fanconi anemia complementation group O |
| Mouse Phenotypes | oligozoospermia |
abnormal spermatocyte morphology |
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| Availability | Mouse Genotype | ||
| Rad51ctm1Sks/Rad51ctm1.1Sks | |||
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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