Gene Expression Literature Detail
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Symbol Name ID |
Larp7
La ribonucleoprotein 7, transcriptional regulator MGI:107634 |
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Reference
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J:190574 Alazami AM, Al-Owain M, Alzahrani F, Shuaib T, Al-Shamrani H, Al-Falki YH, Al-Qahtani SM, Alsheddi T, Colak D, Alkuraya FS, Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism. Hum Mutat. 2012 Oct;33(10):1429-34 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | P |
| 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 | |
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| 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 11/19/2024 MGI 6.24 |
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