Symbol Name ID |
Cep55
centrosomal protein 55 MGI:1921357 |
Darker colors indicate more annotations |
Human Phenotypes | Microretrognathia |
Short neck |
Clinodactyly of the 5th finger |
2-3 toe syndactyly |
Brachydactyly |
Cutaneous syndactyly |
Arthrogryposis multiplex congenita |
Disease(s) Associated with CEP55 | |||||||
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly |
Mouse Phenotypes | abnormal cranium morphology |
abnormal sternum morphology |
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Availability | Mouse Genotype | ||
Cep55tm1a(EUCOMM)Hmgu/Cep55tm1a(EUCOMM)Hmgu | |||
Cep55em1(IMPC)Tcp/Cep55+ |
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 08/02/2024 MGI 6.24 |
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