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Symbol
Name
ID
Grn
granulin
MGI:95832
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Retinal dystrophy
Optic atrophy
Visual impairment
Disease(s) Associated with GRN
neuronal ceroid lipofuscinosis 11

Mouse Phenotypes
abnormal retinal ganglion cell morphology
retinal ganglion cell degeneration
abnormal retinal nerve fiber layer morphology
decreased a wave amplitude
decreased b wave amplitude
abnormal cone electrophysiology
Availability Mouse Genotype
Grntm1.1Far/Grntm1.1Far

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
08/13/2019
MGI 6.14
The Jackson Laboratory