Symbol Name ID |
Vcp
valosin containing protein MGI:99919 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Back pain |
Depression |
Emotional lability |
Atypical behavior |
Personality changes |
Hip pain |
Myalgia |
Disease(s) Associated with VCP | ||||||||
Charcot-Marie-Tooth disease type 2Y | ||||||||
frontotemporal dementia and/or amyotrophic lateral sclerosis 6 | ||||||||
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 | ||||||||
inclusion body myositis |
Mouse Phenotypes | behavior/neurological phenotype |
impaired spatial learning |
increased anxiety-related response |
fast extinction of fear memory |
impaired coordination |
decreased grip strength |
seizures |
tonic-clonic seizures |
|
Availability | Mouse Genotype | ||||||||
Vcptm1Itl/Vcptm1Itl | |||||||||
Vcptm1.1Hiok/Vcp+ | |||||||||
Vcptm1Itl/Vcp+ | * |
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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