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Symbol
Name
ID

Fbn2
fibrillin 2
MGI:95490

Phenotype annotations related to vision/eye

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

Human Phenotypes	Ectopia lentis	Myopia
Disease(s) Associated with FBN2	Ectopia lentis	Myopia
congenital contractural arachnodactyly

Mouse Phenotypes		vision/eye phenotype	abnormal retina blood vessel morphology	corneal vascularization	abnormal optic disk morphology	abnormal eye morphology	abnormal placement of pupils	corneal opacity
Availability	Mouse Genotype	vision/eye phenotype	abnormal retina blood vessel morphology	corneal vascularization	abnormal optic disk morphology	abnormal eye morphology	abnormal placement of pupils	corneal opacity
	Fbn2^{em1(IMPC)Rbrc}/Fbn2^{em1(IMPC)Rbrc}
	Fbn2^fp-4J/Fbn2^fp-4J	*
	Fbn2^timon/Fbn2^timon

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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