Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
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 |
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Availability | Mouse Genotype | |
Pcntem1(IMPC)Mbp/Pcnt+ |
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 09/03/2024 MGI 6.24 |
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