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Symbol Name ID |
Slx4
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) MGI:106299 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Microcephaly |
Bulbous nose |
Blepharophimosis |
Short palpebral fissure |
| Disease(s) Associated with SLX4 | |||||
| Fanconi anemia complementation group P |
| Mouse Phenotypes | abnormal cranium morphology |
enlarged cranium |
abnormal tooth morphology |
domed cranium |
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| Availability | Mouse Genotype | ||||
| Slx4tm1a(EUCOMM)Wtsi/Slx4tm1a(EUCOMM)Wtsi | |||||
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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