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Symbol
Name
ID
Pcnt
pericentrin (kendrin)
MGI:102722
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Sparse scalp hair
Retrognathia
Large sella turcica
Microcephaly
Full cheeks
Sloping forehead
Microdontia
Tooth agenesis
Enamel hypoplasia
Underdeveloped nasal alae
Prominent nasal bridge
Wide nasal bridge
Prominent nose
Aplasia/Hypoplasia of the eyebrow
Narrow palpebral fissure
Downslanted palpebral fissures
Upslanted palpebral fissure
Disease(s) Associated with PCNT
microcephalic osteodysplastic primordial dwarfism type II

Mouse Phenotypes
abnormal craniofacial development
cleft palate
abnormal head shape
Availability Mouse Genotype
PcntGt(RRU388)Byg/PcntGt(RRU388)Byg

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
03/19/2024
MGI 6.23
The Jackson Laboratory