Symbol Name ID |
Grn
granulin MGI:95832 |
Darker colors indicate more annotations |
Human Phenotypes | Optic atrophy |
Retinal dystrophy |
Visual impairment |
Disease(s) Associated with GRN | |||
neuronal ceroid lipofuscinosis 11 |
Mouse Phenotypes | abnormal retina ganglion cell morphology |
retina ganglion cell degeneration |
abnormal retina nerve fiber layer morphology |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal cone electrophysiology |
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Availability | Mouse Genotype | ||||||
Grntm1.1Far/Grntm1.1Far |
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 05/28/2024 MGI 6.13 |
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