Symbol Name ID |
Six2
sine oculis-related homeobox 2 MGI:102778 |
Reference
|
J:326010 Kanda S, Ohmuraya M, Akagawa H, Horita S, Yoshida Y, Kaneko N, Sugawara N, Ishizuka K, Miura K, Harita Y, Yamamoto T, Oka A, Araki K, Furukawa T, Hattori M, Deletion in the Cobalamin Synthetase W Domain-Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract. J Am Soc Nephrol. 2020 Jan;31(1):139-147 |
Age | E11.5 | E12.5 | E13.5 | E16.5 |
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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/21/2024 MGI 6.24 |
![]() |
|