|
Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Patent ductus arteriosus |
Dilatation of the cerebral artery |
Moyamoya phenomenon |
Arterial stenosis |
Vascular dilatation |
Abnormal cerebral vascular morphology |
Stroke |
| Disease(s) Associated with PCNT | ||||||||
| microcephalic osteodysplastic primordial dwarfism type II |
| Mouse Phenotypes | abnormal vascular development |
abnormal heart morphology |
overriding aortic valve |
atrial septal defect |
abnormal heart septum morphology |
atrioventricular septal defect |
ventricular septal defect |
increased heart ventricle size |
hemorrhage |
intracranial hemorrhage |
mitral valve regurgitation |
aortic valve regurgitation |
congestive heart failure |
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| Availability | Mouse Genotype | |||||||||||||
| PcntGt(RRU388)Byg/PcntGt(RRU388)Byg | ||||||||||||||
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 04/16/2024 MGI 6.23 |
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