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Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retrognathia |
Microcephaly |
Full cheeks |
Microdontia |
Tooth agenesis |
Underdeveloped nasal alae |
Wide nasal bridge |
Prominent nose |
Aplasia/Hypoplasia of the eyebrow |
Narrow palpebral fissure |
Downslanted palpebral fissures |
| Disease(s) Associated with PCNT | |||||||||||
| microcephalic osteodysplastic primordial dwarfism type II |
| Mouse Phenotypes | abnormal craniofacial development |
cleft palate |
abnormal head shape |
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| Availability | Mouse Genotype | |||
| PcntGt(RRU388)Byg/PcntGt(RRU388)Byg | ||||
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 07/02/2024 MGI 6.13 |
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