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 |
abnormal female meiosis |
arrest of male meiosis |
|
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 08/02/2024 MGI 6.24 |
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