Symbol Name ID |
Alx4
aristaless-like homeobox 4 MGI:108359 |
Darker colors indicate more annotations |
Human Phenotypes | Shallow orbits |
Optic nerve hypoplasia |
Blue sclerae |
Hypertelorism |
Hypotelorism |
Proptosis |
Microphthalmia |
Strabismus |
Horizontal nystagmus |
Rotary nystagmus |
Vertical nystagmus |
Hypermetropia |
Myopia |
Visual field defect |
Decreased lacrimation |
Ptosis |
Disease(s) Associated with ALX4 | ||||||||||||||||
craniosynostosis | ||||||||||||||||
frontonasal dysplasia 2 | ||||||||||||||||
parietal foramina |
Mouse Phenotypes | cataract |
failure of eyelid fusion |
ocular hypertelorism |
eyelids open at birth |
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Availability | Mouse Genotype | ||||
Alx4Lst-2J/Alx4Lst-2J | |||||
Alx4M1Yzcm/Alx4M1Yzcm | |||||
Alx4Lst-2J/Alx4lst-J |
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 09/03/2024 MGI 6.24 |
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