Symbol Name ID |
Vim
vimentin MGI:98932 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Keratoconjunctivitis sicca |
Pericarditis |
Vasculitis |
Hypertension |
Raynaud phenomenon |
Lymphadenopathy |
Erythema |
Disease(s) Associated with VIM | |||||||
Behcet's disease | |||||||
rheumatoid arthritis | |||||||
Sjogren's syndrome | |||||||
systemic lupus erythematosus |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal blood vessel morphology |
abnormal angiogenesis |
decreased mean systemic arterial blood pressure |
abnormal vasoconstriction |
abnormal vasodilation |
|
Availability | Mouse Genotype | ||||||
Vimtm1Cba/Vimtm1Cba | * | ||||||
Vimtm2Cba/Vimtm2Cba |
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 04/23/2024 MGI 6.23 |
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