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Symbol Name ID |
Cep63
centrosomal protein 63 MGI:2158560 |
| Darker colors indicate more annotations |
| Human Phenotypes | Primary microcephaly |
Delayed speech and language development |
Intellectual disability |
| Disease(s) Associated with CEP63 | |||
| Seckel syndrome 6 |
| Mouse Phenotypes | increased forebrain apoptosis |
abnormal cortical ventricular zone morphology |
decreased forebrain size |
abnormal cerebral cortex morphology |
thin cerebral cortex |
decreased neuronal precursor cell number |
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| Availability | Mouse Genotype | ||||||
| Cep63Gt(EUCE0251h11)Hmgu/Cep63Gt(EUCE0251h11)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 04/30/2024 MGI 6.23 |
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