Symbol Name ID |
Hoxd12
homeobox D12 MGI:96204 |
Reference
|
J:71694 Bruneau S, Johnson KR, Yamamoto M, Kuroiwa A, Duboule D, The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type ii synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes. Dev Biol. 2001 Sep 15;237(2):345-53 |
Age | 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 12/10/2024 MGI 6.24 |
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