|
Symbol Name ID |
Fgfr3
fibroblast growth factor receptor 3 MGI:95524 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Hypertelorism |
Proptosis |
Strabismus |
Visual impairment |
Inflammatory abnormality of the eye |
Ptosis |
| Disease(s) Associated with FGFR3 | |||||||
| Crouzon syndrome-acanthosis nigricans syndrome | |||||||
| Muenke Syndrome | |||||||
| thanatophoric dysplasia |
| Mouse Phenotypes | ocular hypertelorism |
|
| Availability | Mouse Genotype | |
| Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | ||
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 07/02/2024 MGI 6.13 |
|
|
|
||
Analysis Tools