About   Help   FAQ
Symbol
Name
ID
Slx4
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
MGI:106299
Phenotype annotations related to cellular
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
Availability Mouse Genotype
Slx4tm1.2Jrou/Slx4tm1.2Jrou
Slx4tm1a(EUCOMM)Wtsi/Slx4tm1a(EUCOMM)Wtsi
Slx4tm1Jrou/Slx4tm1Jrou

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory