|
Symbol Name ID |
Fgfr3
fibroblast growth factor receptor 3 MGI:95524 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Conjunctivitis |
Cataract |
Optic atrophy |
Optic nerve hypoplasia |
Hypertelorism |
Hypotelorism |
Proptosis |
Strabismus |
Exotropia |
Hypermetropia |
Myopia |
High myopia |
Visual impairment |
Amblyopia |
Visual field defect |
Inflammatory abnormality of the eye |
Alacrima |
Ptosis |
| Disease(s) Associated with FGFR3 | |||||||||||||||||||
| craniosynostosis | |||||||||||||||||||
| Crouzon syndrome-acanthosis nigricans syndrome | |||||||||||||||||||
| lacrimoauriculodentodigital syndrome 2 | |||||||||||||||||||
| Muenke Syndrome | |||||||||||||||||||
| SADDAN | |||||||||||||||||||
| thanatophoric dysplasia |
| Mouse Phenotypes | ocular hypertelorism |
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| 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) |
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last database update 04/30/2024 MGI 6.23 |
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