Gene Expression Literature Detail
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Symbol Name ID |
Foxp2
forkhead box P2 MGI:2148705 |
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Reference
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J:242973 Ravindran E, Hu H, Yuzwa SA, Hernandez-Miranda LR, Kraemer N, Ninnemann O, Musante L, Boltshauser E, Schindler D, Hubner A, Reinecker HC, Ropers HH, Birchmeier C, Miller FD, Wienker TF, Hubner C, Kaindl AM, Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation. PLoS Genet. 2017 Apr;13(4):e1006746 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | P |
| 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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