Gene Expression Literature Detail
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Symbol Name ID |
Prdm16
PR domain containing 16 MGI:1917923 |
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Reference
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J:206694 Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S, Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am J Hum Genet. 2013 Jul 11;93(1):67-77 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E13.5 | P |
| Immunohistochemistry (section) | |
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| In situ RNA (section) | ||
| Immunohistochemistry (whole mount) | ||
| In situ RNA (whole mount) | ||
| 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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