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Symbol
Name
ID
Fgf10
fibroblast growth factor 10
MGI:1099809
Phenotype annotations related to vision/eye
*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
Availability Mouse Genotype
Fgf10tm1Ska/Fgf10tm1Ska
Fgf10tm1Wss/Fgf10tm1Wss
Fgf10Mhdaaey17/Fgf10+ *
Fgf10tm1b(EUCOMM)Wtsi/Fgf10+

Contributing Projects:
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
The Jackson Laboratory