Gene Expression Literature Detail
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Symbol Name ID |
Wnt5a
wingless-type MMTV integration site family, member 5A MGI:98958 |
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Reference
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J:257510 Zhu XJ, Fang Y, Xiong Y, Wang M, Yang X, Li Y, Zhang X, Dai ZM, Qiu M, Zhang Z, Zhang Z, Disruption of Wnt production in Shh lineage causes bone malformation in mice, mimicking human Malik-Percin-type syndactyly. FEBS Lett. 2018 Feb;592(3):356-368 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E11.5 |
| Immunohistochemistry (section) | ||
| In situ RNA (section) | ||
| Immunohistochemistry (whole mount) | ||
| In situ RNA (whole mount) | |
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| In situ reporter (knock in) | ||
| Northern blot | ||
| Western blot | ||
| RT-PCR | ||
| cDNA clones | ||
| RNase protection | ||
| Nuclease S1 | ||
| Primer Extension |
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 11/12/2024 MGI 6.24 |
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