Symbol Name ID |
Cenpj
centromere protein J MGI:2684927 |
Darker colors indicate more annotations |
Human Phenotypes | Retrognathia |
Microcephaly |
High forehead |
Sloping forehead |
Thin upper lip vermilion |
Underdeveloped nasal alae |
Bifid nasal tip |
Upslanted palpebral fissure |
Disease(s) Associated with CENPJ | ||||||||
primary autosomal recessive microcephaly | ||||||||
primary autosomal recessive microcephaly 6 | ||||||||
Seckel syndrome 4 |
Mouse Phenotypes | abnormal cranium morphology |
decreased cranium length |
small cranium |
abnormal occipital bone morphology |
abnormal parietal bone morphology |
sloping forehead |
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Availability | Mouse Genotype | ||||||
Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi |
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 04/09/2024 MGI 6.23 |
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