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Symbol Name ID |
Copb2
COPI coat complex subunit beta 2 MGI:1354962 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Delayed CNS myelination |
Ventriculomegaly |
Simplified gyral pattern |
Hypoplasia of the corpus callosum |
Extra-axial cerebrospinal fluid accumulation |
Severe global developmental delay |
| Disease(s) Associated with COPB2 | ||||||||
| primary autosomal recessive microcephaly 19 |
| Mouse Phenotypes | increased neuron apoptosis |
abnormal neuron proliferation |
increased neuronal precursor proliferation |
decreased brain weight |
abnormal cerebral cortex morphology |
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| Availability | Mouse Genotype | |||||
| Copb2em1Rstot/Copb2em2Rstot | ||||||
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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