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Symbol Name ID |
Caprin2
caprin family member 2 MGI:2448541 |
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Reference
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J:225905 Dash S, Dang CA, Beebe DC, Lachke SA, Deficiency of the RNA binding protein caprin2 causes lens defects and features of peters anomaly. Dev Dyn. 2015 Oct;244(10):1313-27 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E12.5 | E13.5 | E14.5 | E15.5 | E19.5 | P |
| Immunohistochemistry (section) | ![]() |
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| In situ RNA (section) | ![]() |
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| Immunohistochemistry (whole mount) | |||||||
| In situ RNA (whole mount) | |||||||
| In situ reporter (knock in) | |||||||
| Northern blot | |||||||
| Western blot | ![]() |
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| RT-PCR | ![]() |
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| 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 09/30/2025 MGI 6.24 |
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