Symbol Name ID |
Cdon
cell adhesion molecule-related/down-regulated by oncogenes MGI:1926387 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Disease(s) Associated with CDON | |
holoprosencephaly 11 |
Mouse Phenotypes | basisphenoid bone foramen |
small basisphenoid bone |
abnormal upper incisor morphology |
absent upper incisors |
abnormal maxilla morphology |
abnormal maxillary shelf morphology |
absent maxillary shelf |
decreased maxillary shelf size |
abnormal premaxilla morphology |
domed cranium |
absent nasal septum cartilage |
nasal septum cartilage hypoplasia |
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Availability | Mouse Genotype | ||||||||||||
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 04/30/2024 MGI 6.23 |
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