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Symbol
Name
ID
Pcnt
pericentrin (kendrin)
MGI:102722
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Sparse scalp hair
Aplasia/Hypoplasia of the eyebrow
Fine hair
Cafe-au-lait spot
Multiple cafe-au-lait spots
Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines
Hypopigmented skin patches
Dry skin
Disease(s) Associated with PCNT
microcephalic osteodysplastic primordial dwarfism type II

Mouse Phenotypes
abnormal skin morphology
Availability Mouse Genotype
Pcntem1(IMPC)Mbp/Pcnt+

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