Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
Darker colors indicate more annotations |
Human Phenotypes | Hypermetropia |
Disease(s) Associated with PCNT | |
microcephalic osteodysplastic primordial dwarfism type II |
Mouse Phenotypes | abnormal eye morphology |
cataract |
persistence of hyaloid vascular system |
microphthalmia |
abnormal vitreous body morphology |
anophthalmia |
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Availability | Mouse Genotype | ||||||
Pcntem1(IMPC)Mbp/Pcntem1(IMPC)Mbp | |||||||
PcntGt(RRU388)Byg/PcntGt(RRU388)Byg | |||||||
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 08/02/2024 MGI 6.24 |
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