Gene Expression Literature Detail
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Symbol Name ID |
Foxa2
forkhead box A2 MGI:1347476 |
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Reference
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J:249891 Giri D, Vignola ML, Gualtieri A, Scagliotti V, McNamara P, Peak M, Didi M, Gaston-Massuet C, Senniappan S, Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities. Hum Mol Genet. 2017 Nov 15;26(22):4315-4326 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E11.5 | E12.5 | E13.5 | E15.5 | E18.5 |
| 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 09/30/2025 MGI 6.24 |
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