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Symbol Name ID |
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| Synonyms | CCN6, LOC327743 | ||||||||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||||||||
| Genetic Map | |||||||||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:77038 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 chicken; 1 zebrafish Protein SuperFamily: IGFBP-related protein, CNN type Gene Tree: Wisp3 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(4) :
Targeted(4)
Homozygous null mice are viable and fertile with no obvious abnormalities in size, weight, skeletal development, ossification, or the occurrence of joint disease. |
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Gene Ontology (GO) classifications |
All GO classifications: (7 annotations)
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| Expression |
Literature Summary: (3 records) Data Summary: Results (8) Tissues (6) Images (7) Theiler Stages: 11, 17, 19, 20, 21, 23
External Resources: GEO ArrayExpress |
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Molecular reagents |
All nucleic(3)
cDNA(1)
Primer pair(2)
Microarray probesets(1) |
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Other database links |
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| Sequences |
All sequences(8) RefSeq(3) UniProt(1) |
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Protein-related information |
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| References |
(Earliest) J:94500
Kutz WE, et al., WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice. Mol Cell Biol. 2005 Jan;25(1):414-21 (Latest) J:165751 Du J, et al., O-fucosylation of thrombospondin type 1 repeats restricts epithelial to mesenchymal transition (EMT) and maintains epiblast pluripotency during mouse gastrulation. Dev Biol. 2010 Oct 1;346(1):25-38 All references(21) |
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Other accession IDs |
MGI:3641683 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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