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Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Micrognathia	Microcephaly	Absent thumb	Short thumb	Hypoplasia of the radius
Disease(s) Associated with SLX4
Fanconi anemia complementation group P

Mouse Phenotypes		abnormal cranium morphology	enlarged cranium	abnormal tooth morphology	domed cranium	increased caudal vertebrae number	abnormal spine curvature	vertebral fusion	increased bone mineral density
Availability	Mouse Genotype	abnormal cranium morphology	enlarged cranium	abnormal tooth morphology	domed cranium	increased caudal vertebrae number	abnormal spine curvature	vertebral fusion	increased bone mineral density
	Slx4^{tm1a(EUCOMM)Wtsi}/Slx4^{tm1a(EUCOMM)Wtsi}
	Slx4^{tm1a(EUCOMM)Wtsi}/Slx4⁺

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)
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