Symbol Name ID |
Slx4
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) MGI:106299 |
Darker colors indicate more annotations |
Human Phenotypes | Chromosomal breakage induced by crosslinking agents |
Disease(s) Associated with SLX4 | |
Fanconi anemia complementation group P |
Mouse Phenotypes | absent oocytes |
azoospermia |
oligozoospermia |
abnormal primordial germ cell morphology |
abnormal telomere morphology |
increased sensitivity to induced cell death |
abnormal male germ cell apoptosis |
early cellular replicative senescence |
abnormal DNA repair |
chromosomal instability |
induced chromosome breakage |
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Availability | Mouse Genotype | |||||||||||
Slx4tm1.2Jrou/Slx4tm1.2Jrou | ||||||||||||
Slx4tm1a(EUCOMM)Wtsi/Slx4tm1a(EUCOMM)Wtsi | ||||||||||||
Slx4tm1Jrou/Slx4tm1Jrou |
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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