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Symbol
Name
ID
Pcnt
pericentrin (kendrin)
MGI:102722
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Attention deficit hyperactivity disorder
Hypernasal speech
Disease(s) Associated with PCNT
microcephalic osteodysplastic primordial dwarfism type II

Mouse Phenotypes
sporadic seizures
Availability Mouse Genotype
Pcntm239Asp/Pcnt+
Tg(Rr291-lacZ)#Mekk/0
Pcntm275Asp/Pcnt+
Tg(Rr291-lacZ)#Mekk/0

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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory