|
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 |
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| 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) |
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last database update 04/23/2024 MGI 6.23 |
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