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Symbol Name ID |
Msx2
msh homeobox 2 MGI:97169 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Optic nerve hypoplasia |
Blue sclerae |
Hypertelorism |
Hypotelorism |
Proptosis |
Strabismus |
Hypermetropia |
Myopia |
Visual field defect |
Ptosis |
| Disease(s) Associated with MSX2 | |||||||||||
| craniosynostosis | |||||||||||
| parietal foramina |
| Mouse Phenotypes | abnormal retina pigment epithelium morphology |
abnormal eye morphology |
iris hyperplasia |
anterior iris synechia |
abnormal cornea morphology |
increased cornea thickness |
decreased corneal epithelium thickness |
increased corneal stroma thickness |
corneal opacity |
abnormal lens morphology |
abnormal lens vesicle development |
small lens |
abnormal eye development |
abnormal optic vesicle formation |
microphthalmia |
narrow eye opening |
retina fold |
vitreous body deposition |
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| Availability | Mouse Genotype | ||||||||||||||||||
| Msx2m1Btlr/Msx2m1Btlr | |||||||||||||||||||
| Msx2tm1Rilm/Msx2tm1Rilm | |||||||||||||||||||
| Tg(Msx2)1Rem/0 | |||||||||||||||||||
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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