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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 |
persistence of hyaloid vascular system |
microphthalmia |
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 04/16/2024 MGI 6.23 |
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