Symbol Name ID |
Cenpe
centromere protein E MGI:1098230 |
Darker colors indicate more annotations |
Human Phenotypes | Nystagmus |
Disease(s) Associated with CENPE | |
primary autosomal recessive microcephaly 13 |
Mouse Phenotypes | abnormal lens morphology |
cataract |
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Availability | Mouse Genotype | ||
Cenpetm1b(EUCOMM)Hmgu/Cenpe+ |
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 09/03/2024 MGI 6.24 |
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