Gene Expression Literature Detail
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Symbol Name ID |
Cux1
cut-like homeobox 1 MGI:88568 |
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Reference
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J:324458 Roque M, Alves Rodrigues de Souza D, Rangel-Sosa MM, Altounian M, Hocine M, Deloulme JC, Barbier EL, Mann F, Chauvet S, VPS35 deficiency in the embryonic cortex leads to prenatal cell loss and abnormal development of axonal connectivity. Mol Cell Neurosci. 2022 Mar 31;120:103726 |
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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