About   Help   FAQ
Symbol
Name
ID
Vwf
Von Willebrand factor
MGI:98941
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Gastrointestinal hemorrhage
Hematemesis
Joint hemorrhage
Bruising susceptibility
Purpura
Petechiae
Spontaneous hematomas
Mitral valve prolapse
Peripheral arterial stenosis
Abnormal cerebral vascular morphology
Ischemic stroke
Transient ischemic attack
Gastrointestinal angiodysplasia
Aortic valve stenosis
Raynaud phenomenon
Cerebral ischemia
Pulmonary arterial hypertension
Myocardial infarction
Syncope
Splenomegaly
Erythema
Disease(s) Associated with VWF
Behcet's disease
Bernard-Soulier syndrome
essential thrombocythemia
von Willebrand's disease 1
von Willebrand's disease 2
von Willebrand's disease 3

Mouse Phenotypes
internal hemorrhage
decreased myocardial infarct size
impaired blood-brain barrier function
Availability Mouse Genotype
Vwftm1Wgr/Vwftm1Wgr

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory