Symbol Name ID |
Grhl2
grainyhead like transcription factor 2 MGI:2182543 |
Reference
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J:343442 Crane-Smith Z, De Castro SCP, Nikolopoulou E, Wolujewicz P, Smedley D, Lei Y, Mather E, Santos C, Hopkinson M, Pitsillides AA, Finnell RH, Ross ME, Copp AJ, Greene NDE, A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele. Hum Mol Genet. 2023 Aug 26;32(17):2681-2692 |
Age | E9.5 | E11.5 |
Immunohistochemistry (section) | ||
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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