|
Symbol Name ID |
Cenpj
centromere protein J MGI:2684927 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Ventriculomegaly |
Pachygyria |
Hypoplasia of the frontal lobes |
Small cerebral cortex |
Agenesis of corpus callosum |
Gray matter heterotopia |
Absent speech |
Intellectual disability, mild |
Intellectual disability, moderate |
Intellectual disability, severe |
Hyperreflexia |
Global developmental delay |
Seizure |
| Disease(s) Associated with CENPJ | ||||||||||||||
| primary autosomal recessive microcephaly | ||||||||||||||
| primary autosomal recessive microcephaly 6 | ||||||||||||||
| Seckel syndrome 4 |
| Mouse Phenotypes | nervous system phenotype |
decreased brain weight |
abnormal dentate gyrus morphology |
decreased neuron number |
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| Availability | Mouse Genotype | ||||
| Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi | * | ||||
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 04/23/2024 MGI 6.23 |
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