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 | Anorexia |
Abnormality of the nervous system |
Chorea |
Depression |
Irritability |
Psychosis |
Seizure |
Disease(s) Associated with VIM | |||||||
Behcet's disease | |||||||
systemic lupus erythematosus |
Mouse Phenotypes | nervous system phenotype |
abnormal cerebellum morphology |
abnormal cerebellar Purkinje cell layer |
abnormal Purkinje cell morphology |
Purkinje cell degeneration |
abnormal Purkinje cell dendrite morphology |
decreased Purkinje cell number |
abnormal astrocyte morphology |
|
Availability | Mouse Genotype | ||||||||
Vimtm1Cba/Vimtm1Cba | * |
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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