Symbol Name ID |
Fanca
Fanconi anemia, complementation group A MGI:1341823 |
! | Indicates phenotype varies with strain background. |
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 FANCA | ||||
Fanconi anemia | ||||
Fanconi anemia complementation group A |
Mouse Phenotypes | decreased germ cell number |
abnormal chromosome morphology |
abnormal cell physiology |
increased sensitivity to induced cell death |
increased male germ cell apoptosis |
chromosome breakage |
induced chromosome breakage |
spontaneous chromosome breakage |
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Availability | Mouse Genotype | ||||||||
Fancatm1.1Wong/Fancatm1.1Wong | |||||||||
Fancatm1a(EUCOMM)Wtsi/Fancatm1a(EUCOMM)Wtsi | |||||||||
Fancatm1Faw/Fancatm1Faw | |||||||||
Fancatm1Wong/Fancatm1Wong | ! | ||||||||
Fancatm1Zqw/Fancatm1Zqw | |||||||||
Fancatm1Faw/Fanca+ |
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 04/16/2024 MGI 6.23 |
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