Symbol Name ID |
Cenpf
centromere protein F MGI:1313302 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Accessory spleen |
Retinal vascular tortuosity |
Disease(s) Associated with CENPF | ||
Stromme syndrome |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal myocardial fiber morphology |
abnormal intercalated disk morphology |
myocardial trabeculae hypoplasia |
abnormal heart morphology |
abnormal heart atrium morphology |
decreased heart weight |
small heart |
abnormal heart ventricle morphology |
dilated heart left ventricle |
thin ventricular wall |
abnormal epicardium morphology |
cardiac fibrosis |
dilated cardiomyopathy |
abnormal cardiovascular system physiology |
decreased fetal cardiomyocyte proliferation |
prolonged PR interval |
abnormal heart electrocardiography waveform feature |
prolonged P wave |
abnormal myocardial fiber physiology |
|
Availability | Mouse Genotype | ||||||||||||||||||||
Cenpftm1Dbdr/Cenpftm1Dbdr Tg(Tnnt2-cre)5Blh/0 (conditional) |
* |
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 05/14/2024 MGI 6.23 |
|
|