About Help FAQ

Symbol
Name
ID

Slx4
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
MGI:106299

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Microcephaly
Disease(s) Associated with SLX4	Microcephaly
Fanconi anemia complementation group P

Mouse Phenotypes		nervous system phenotype	hydrocephaly	obstructive hydrocephaly	dilated lateral ventricle	abnormal third ventricle morphology	abnormal cerebral cortex morphology	thin cerebral cortex	absent optic nerve
Availability	Mouse Genotype
	Slx4^{tm1a(EUCOMM)Wtsi}/Slx4^{tm1a(EUCOMM)Wtsi}	*

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