Symbol Name ID |
Fgf9
fibroblast growth factor 9 MGI:104723 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Proptosis |
Disease(s) Associated with FGF9 | |
multiple synostoses syndrome 3 |
Mouse Phenotypes | vision/eye phenotype |
abnormal retina vasculature morphology |
increased eye anterior chamber depth |
abnormal lens development |
cataract |
small lens |
exophthalmos |
ocular hypertelorism |
abnormal vision |
|
Availability | Mouse Genotype | |||||||||
Fgf9Aca12/Fgf9Aca12 | * | |||||||||
Fgf9Eks/Fgf9Eks | ||||||||||
Fgf9Aca12/Fgf9+ | * | |||||||||
Fgf9tm1b(KOMP)Wtsi/Fgf9+ |
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 04/23/2024 MGI 6.23 |
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