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 agents |
increased cellular sensitivity to ionizing radiation |
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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 08/02/2024 MGI 6.24 |
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