Symbol Name ID |
Cdon
cell adhesion molecule-related/down-regulated by oncogenes MGI:1926387 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Agenesis of corpus callosum |
Holoprosencephaly |
Global developmental delay |
Disease(s) Associated with CDON | ||||
holoprosencephaly 11 |
Mouse Phenotypes | nervous system phenotype |
abnormal neuronal precursor proliferation |
absent lamina terminalis |
holoprosencephaly |
hydrocephaly |
abnormal brain ventricle morphology |
enlarged lateral ventricles |
abnormal forebrain morphology |
abnormal cerebral cortex morphology |
thin cerebral cortex |
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Availability | Mouse Genotype | ||||||||||
Cdontm1Aok/Cdontm1Aok | * | ||||||||||
Cdontm1Rsk/Cdontm1Rsk | |||||||||||
Cdontm2Rsk/Cdontm2Rsk |
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 05/14/2024 MGI 6.23 |
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