Symbol Name ID |
Dennd2b
DENN domain containing 2B MGI:108517 |
Reference
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J:157306 Gohring I, Tagariello A, Endele S, Stolt CC, Ghassibe M, Fisher M, Thiel CT, Trautmann U, Vikkula M, Winterpacht A, FitzPatrick DR, Rauch A, Disruption of ST5 is associated with mental retardation and multiple congenital anomalies. J Med Genet. 2010 Feb;47(2):91-8 |
Age | E8.5 | E9.5 | E11.5 | E13.5 | E15 | E15.5 | P |
Immunohistochemistry (section) | |||||||
In situ RNA (section) | ![]() |
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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 12/10/2024 MGI 6.24 |
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