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Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Disproportionate short stature |
Truncal obesity |
Intrauterine growth retardation |
Postnatal growth retardation |
| Disease(s) Associated with PCNT | ||||
| microcephalic osteodysplastic primordial dwarfism type II |
| Mouse Phenotypes | cleft palate |
abnormal head shape |
embryonic growth retardation |
kidney cyst |
kidney cortex cyst |
renal glomerulus cyst |
microcephaly |
decreased body length |
prenatal growth retardation |
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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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