Symbol Name ID |
Fgf10
fibroblast growth factor 10 MGI:1099809 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Esotropia |
Alacrima |
Disease(s) Associated with FGF10 | ||
lacrimoauriculodentodigital syndrome 3 |
Mouse Phenotypes | vision/eye phenotype |
impaired pupillary reflex |
abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal retina apoptosis |
absent lacrimal glands |
abnormal optic disk morphology |
abnormal iris pigmentation |
abnormal placement of pupils |
iris synechia |
abnormal cornea morphology |
corneal opacity |
fused cornea and lens |
abnormal lens morphology |
abnormal lens epithelium morphology |
abnormal lens fiber morphology |
cataract |
persistence of hyaloid vascular system |
microphthalmia |
narrow eye opening |
eyelids open at birth |
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Availability | Mouse Genotype | |||||||||||||||||||||
Fgf10tm1Ska/Fgf10tm1Ska | ||||||||||||||||||||||
Fgf10tm1Wss/Fgf10tm1Wss | ||||||||||||||||||||||
Fgf10Mhdaaey17/Fgf10+ | * | |||||||||||||||||||||
Fgf10tm1b(EUCOMM)Wtsi/Fgf10+ |
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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