Symbol Name ID |
Wnt1
wingless-type MMTV integration site family, member 1 MGI:98953 |
Reference
|
J:335098 Han F, Yang B, Chen Y, Liu L, Cheng X, Huang J, Zhou K, Zhang D, Xu E, Lai M, Lv B, Cheng H, Zhang H, Loss of GLTSCR1 causes congenital heart defects by regulating NPPA transcription. Angiogenesis. 2023 May;26(2):217-232 |
Age | E11.5 | E13 | E15 | E16.5 | E18 |
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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 11/19/2024 MGI 6.24 |
|
|