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Symbol Name ID |
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| Synonyms | CAM-related/down-regulated by oncogenes, CDO | ||||||||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||||||||
| Genetic Map | |||||||||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:22996 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 1 zebrafish Gene Tree: Cdon |
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| Human homologs |
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Alleles and phenotypes |
All alleles(8) :
Targeted(5)
Gene trapped(3)
Homozygous null mice display facial defects characteristic of microform holoprosencephaly, are runted, and are prone to death prior to weaning. Human Diseases Modeled Using Mouse Cdon (1) Alleles Annotated to Human Diseases(2) |
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Gene Ontology (GO) classifications |
All GO classifications: (39 annotations)
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| Expression |
Literature Summary: (16 records) Data Summary: Results (212) Tissues (154) Images (40) Theiler Stages: 9, 11, 13, 15, 17, 19, 20, 21, 23, 24, 25, 28
External Resources: Allen Institute GENSAT GEO ArrayExpress |
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Molecular reagents |
All nucleic(83)
cDNA(83)
Microarray probesets(3) |
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Other database links |
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| Sequences |
All sequences(51) RefSeq(2) UniProt(6) |
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| Polymorphisms | SNPs(492 from dbSNP Build 128) | ||||||||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:65661
Kang JS, et al., CDO: an oncogene-, serum-, and anchorage-regulated member of the Ig/fibronectin type III repeat family. J Cell Biol. 1997 Jul 14;138(1):203-13 (Latest) J:193728 Hong M, et al., Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice. PLoS Genet. 2012;8(10):e1002999 All references(56) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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