|
Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Dilatation of the cerebral artery |
Moyamoya phenomenon |
Abnormal cerebral vascular morphology |
Stroke |
Ventriculomegaly |
Hypoplasia of the corpus callosum |
High pitched voice |
Attention deficit hyperactivity disorder |
Intellectual disability |
Global developmental delay |
Seizure |
| Disease(s) Associated with PCNT | ||||||||||||
| microcephalic osteodysplastic primordial dwarfism type II |
| Mouse Phenotypes | sporadic seizures |
intracranial hemorrhage |
abnormal neuron differentiation |
abnormal embryonic neuroepithelium morphology |
abnormal brain development |
thin cortical plate |
abnormal cortical ventricular zone morphology |
decreased brain size |
enlarged brain ventricles |
abnormal hippocampus morphology |
abnormal cerebral cortex morphology |
thin cerebral cortex |
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| Availability | Mouse Genotype | ||||||||||||
| PcntGt(RRU388)Byg/PcntGt(RRU388)Byg | |||||||||||||
| Pcntm239Asp/Pcntm239Asp Tg(Rr291-lacZ)#Mekk/0 |
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| Pcntm275Asp/Pcntm275Asp Tg(Rr291-lacZ)#Mekk/0 |
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| Pcntm239Asp/Pcnt+ Tg(Rr291-lacZ)#Mekk/0 |
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| Pcntm275Asp/Pcnt+ Tg(Rr291-lacZ)#Mekk/0 |
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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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