Symbol Name ID |
Cep55
centrosomal protein 55 MGI:1921357 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microretrognathia |
Potter facies |
Choanal stenosis |
Anteverted nares |
Narrow nasal ridge |
Bulbous nose |
Narrow palpebral fissure |
Disease(s) Associated with CEP55 | |||||||
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly |
Mouse Phenotypes | craniofacial phenotype |
abnormal cranium morphology |
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Availability | Mouse Genotype | ||
Cep55em1.1Hyli/Cep55em1.1Hyli | * | ||
Cep55tm1a(EUCOMM)Hmgu/Cep55tm1a(EUCOMM)Hmgu |
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 |
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