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Symbol Name ID |
Avp
arginine vasopressin MGI:88121 |
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Reference
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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 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E17.5 | P |
| Immunohistochemistry (section) | ![]() |
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| In situ RNA (section) | ![]() |
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| 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 09/30/2025 MGI 6.24 |
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