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 | abnormal DNA repair |
increased circulating follicle stimulating hormone level |
increased circulating luteinizing hormone level |
increased physiological sensitivity to xenobiotic |
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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 09/03/2024 MGI 6.24 |
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