Symbol Name ID |
Vim
vimentin MGI:98932 |
Darker colors indicate more annotations |
Human Phenotypes | Keratoconjunctivitis sicca |
Hypopyon |
Posterior polar cataract |
Diffuse nuclear cataract |
Pulverulent cataract |
Iritis |
Chorioretinitis |
Retinopathy |
Iridocyclitis |
Disease(s) Associated with VIM | |||||||||
Behcet's disease | |||||||||
cataract 30 | |||||||||
Sjogren's syndrome | |||||||||
systemic lupus erythematosus |
Mouse Phenotypes | ruptured lens capsule |
abnormal lens fiber morphology |
disorganized secondary lens fibers |
cataract |
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Availability | Mouse Genotype | ||||
Tg(Vim*R113C)1Tmm/0 |
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 05/14/2024 MGI 6.23 |
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