Symbol Name ID |
Oxt
oxytocin MGI:97453 |
Reference
|
J:178252 McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT, Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction. J Clin Endocrinol Metab. 2011 Oct;96(10):E1709-18 |
Age | E17.5 |
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) |
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last database update 11/19/2024 MGI 6.24 |
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