Symbol Name ID |
Pcnt
pericentrin (kendrin) MGI:102722 |
Darker colors indicate more annotations |
Human Phenotypes | Sparse scalp hair |
Retrognathia |
Large sella turcica |
Microcephaly |
Full cheeks |
Sloping forehead |
Microdontia |
Tooth agenesis |
Enamel hypoplasia |
Underdeveloped nasal alae |
Prominent nasal bridge |
Wide nasal bridge |
Prominent nose |
Aplasia/Hypoplasia of the eyebrow |
Narrow palpebral fissure |
Downslanted palpebral fissures |
Upslanted palpebral fissure |
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 03/19/2024 MGI 6.23 |
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