Symbol Name ID |
Sox2
SRY (sex determining region Y)-box 2 MGI:98364 |
Reference
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J:321206 Chen J, Lambo ME, Ge X, Dearborn JT, Liu Y, McCullough KB, Swift RG, Tabachnick DR, Tian L, Noguchi K, Garbow JR, Constantino JN, Gabel HW, Hengen KB, Maloney SE, Dougherty JD, A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation. Neuron. 2021 Dec 1;109(23):3775-3792.e14 |
Age | E14 | 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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