|
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 |
|
| 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/09/2024 MGI 6.23 |
|
|
|
||
Analysis Tools