Symbol Name ID |
Sox21
SRY (sex determining region Y)-box 21 MGI:2654070 |
Reference
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J:355488 Erjavec E, Angee C, Hadjadj D, Passet B, David P, Kostic C, Dode E, Zanlonghi X, Cagnard N, Nedelec B, Crippa SV, Bole-Feysot C, Zarhrate M, Creuzet S, Castille J, Vilotte JL, Calvas P, Plaisancie J, Chassaing N, Kaplan J, Rozet JM, Taie LF, Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia. Am J Hum Genet. 2024 Oct 3;111(10):2265-2282 |
Age | E10 | E10.5 | E11 | E11.5 | E12.5 | E13.5 | E15.5 | E17.5 | E18.5 | 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 12/10/2024 MGI 6.24 |
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