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Symbol Name ID |
Mlc1
megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) MGI:2157910 |
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Reference
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J:377054 Hinckelmann MV, Dubos A, Artot V, Rudolf G, Nguyen TL, Tilly P, Nalesso V, Muniz Moreno MDM, Birling MC, Godin JD, Brault V, Herault Y, Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis. Mol Psychiatry. 2025 Nov;30(11):5227-5244 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E14.5 |
| 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 01/13/2026 MGI 6.24 |
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