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Symbol Name ID |
Fancf
Fanconi anemia, complementation group F MGI:3689889 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chromosomal breakage induced by crosslinking agents |
| Disease(s) Associated with FANCF | |
| Fanconi anemia complementation group F |
| Mouse Phenotypes | azoospermia |
polyploidy |
abnormal DNA repair |
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| Availability | Mouse Genotype | |||
| Fancftm1Nki/Fancftm1Nki | ||||
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 04/09/2024 MGI 6.23 |
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