Symbol Name ID |
Wnt1
wingless-type MMTV integration site family, member 1 MGI:98953 |
Reference
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J:203641 Keupp K, Beleggia F, Kayserili H, Barnes AM, Steiner M, Semler O, Fischer B, Yigit G, Janda CY, Becker J, Breer S, Altunoglu U, Grunhagen J, Krawitz P, Hecht J, Schinke T, Makareeva E, Lausch E, Cankaya T, Caparros-Martin JA, Lapunzina P, Temtamy S, Aglan M, Zabel B, Eysel P, Koerber F, Leikin S, Garcia KC, Netzer C, Schonau E, Ruiz-Perez VL, Mundlos S, Amling M, Kornak U, Marini J, Wollnik B, Mutations in WNT1 cause different forms of bone fragility. Am J Hum Genet. 2013 Apr 4;92(4):565-74 |
Age | E14.5 | 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 11/19/2024 MGI 6.24 |
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