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Symbol Name ID |
Fancd2
Fanconi anemia, complementation group D2 MGI:2448480 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of chromosome stability |
Chromosomal breakage induced by crosslinking agents |
Deficient excision of UV-induced pyrimidine dimers in DNA |
Prolonged G2 phase of cell cycle |
| Disease(s) Associated with FANCD2 | ||||
| Fanconi anemia | ||||
| Fanconi anemia complementation group D2 |
| Mouse Phenotypes | azoospermia |
oligozoospermia |
abnormal spermatocyte morphology |
abnormal male meiosis |
increased sensitivity to induced cell death |
increased cellular sensitivity to DNA damaging agent induced cell death |
increased cellular sensitivity to ionizing radiation induced cell death |
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| Availability | Mouse Genotype | |||||||
| Fancd2em1Tzh/Fancd2em1Tzh | ||||||||
| Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex | ||||||||
| Fancd2tm1Hou/Fancd2tm1Hou | ||||||||
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 06/09/2026 MGI 6.24 |
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