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Symbol Name ID |
Hmx1
H6 homeobox 1 MGI:107178 |
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Reference
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J:139285 Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL, Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome. Am J Hum Genet. 2008 May;82(5):1178-84 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E13.5 | E18.5 | E | P |
| Immunohistochemistry (section) | |||||
| In situ RNA (section) | ![]() |
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| 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 12/30/2025 MGI 6.24 |
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