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Symbol
Name
ID

Fgf9
fibroblast growth factor 9
MGI:104723

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Proptosis
Disease(s) Associated with FGF9	Proptosis
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	vision/eye phenotype	abnormal retina vasculature morphology	increased eye anterior chamber depth	abnormal lens development	cataract	small lens	exophthalmos	ocular hypertelorism	abnormal vision
	Fgf9^Aca12/Fgf9^Aca12	*
	Fgf9^Eks/Fgf9^Eks
	Fgf9^Aca12/Fgf9⁺	*
	Fgf9^{tm1b(KOMP)Wtsi}/Fgf9⁺

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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