Symbol Name ID |
Wrn
Werner syndrome RecQ like helicase MGI:109635 |
Darker colors indicate more annotations |
Human Phenotypes | Pulmonary artery stenosis |
Atherosclerosis |
Abnormal cerebral vascular morphology |
Hypertension |
Myocardial infarction |
Congestive heart failure |
Telangiectasia of the skin |
Disease(s) Associated with WRN | |||||||
Werner syndrome |
Mouse Phenotypes | abnormal cardiovascular development |
bicuspid aortic valve |
aortic valve stenosis |
bicuspid pulmonary valve |
cardiac interstitial fibrosis |
increased left ventricle systolic pressure |
decreased systemic arterial diastolic blood pressure |
heart inflammation |
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Availability | Mouse Genotype | ||||||||
Wrnb2b3121.1Clo/Wrnb2b3121.1Clo | |||||||||
Wrntm1Led/Wrntm1Led | |||||||||
Wrntm1Led/Wrn+ |
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 06/12/2024 MGI 6.13 |
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