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Symbol
Name
ID
Cep55
centrosomal protein 55
MGI:1921357
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Oligohydramnios
Disease(s) Associated with CEP55
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly

Mouse Phenotypes
abnormal embryonic neuroepithelium primary cilium morphology
Availability Mouse Genotype
Cep55em1.1Hyli/Cep55em1.1Hyli

Contributing Projects:
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
The Jackson Laboratory