Symbol Name ID |
Cav1
caveolin 1, caveolae protein MGI:102709 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of chromosome stability |
Chromosome breakage |
Disease(s) Associated with CAV1 | ||
systemic scleroderma |
Mouse Phenotypes | cellular phenotype |
abnormal cell morphology |
abnormal cell cytoskeleton morphology |
abnormal actin cytoskeleton morphology |
abnormal microtubule organizing center morphology |
absent caveolae |
abnormal fibroblast chemotaxis |
decreased fibroblast chemotaxis |
increased lung endothelial cell proliferation |
decreased hepatocyte proliferation |
abnormal cellular cholesterol metabolism |
abnormal cellular respiration |
abnormal respiratory electron transport chain |
abnormal vesicle-mediated transport |
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Availability | Mouse Genotype | ||||||||||||||
Cav1tm1Krc/Cav1tm1Krc | |||||||||||||||
Cav1tm1Kur/Cav1tm1Kur | * | ||||||||||||||
Cav1tm1Mls/Cav1tm1Mls |
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 04/09/2024 MGI 6.23 |
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