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Symbol
Name
ID

Fmr1
fragile X messenger ribonucleoprotein 1
MGI:95564

Phenotype annotations related to vision/eye

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

Human Phenotypes	Strabismus	Nystagmus	Saccadic smooth pursuit
Disease(s) Associated with FMR1	Strabismus	Nystagmus	Saccadic smooth pursuit
fragile X syndrome
fragile X-associated tremor/ataxia syndrome

Mouse Phenotypes		vision/eye phenotype	abnormal retina rod cell outer segment morphology	abnormal retina morphology	decreased a-wave amplitude	decreased b-wave amplitude
Availability	Mouse Genotype
	Fmr1^tm1Cgr/Y	*

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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