Symbol Name ID |
Hey1
hairy/enhancer-of-split related with YRPW motif 1 MGI:1341800 |
Reference
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J:133699 Fischer A, Steidl C, Wagner TU, Lang E, Jakob PM, Friedl P, Knobeloch KP, Gessler M, Combined loss of Hey1 and HeyL causes congenital heart defects because of impaired epithelial to mesenchymal transition. Circ Res. 2007 Mar 30;100(6):856-63 |
Age | E9.5 | E10.5 | E12.5 | E |
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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