|
Symbol Name ID |
Alx3
aristaless-like homeobox 3 MGI:1277097 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
Hypertelorism |
Microphthalmia |
Coloboma |
Ptosis |
| Disease(s) Associated with ALX3 | |||||
| frontonasal dysplasia 1 |
| Mouse Phenotypes | failure of eyelid fusion |
|
| Availability | Mouse Genotype | |
| Alx3tm1Hubr/Alx3tm1Hubr | ||
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 |
|
|
|
||
Analysis Tools