Gene Expression Literature Detail
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Symbol Name ID |
Gnrh1
gonadotropin releasing hormone 1 MGI:95789 |
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Reference
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J:127117 Pitteloud N, Zhang C, Pignatelli D, Li JD, Raivio T, Cole LW, Plummer L, Jacobson-Dickman EE, Mellon PL, Zhou QY, Crowley WF Jr, Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc Natl Acad Sci U S A. 2007 Oct 30;104(44):17447-52 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E13.5 | E16.5 | E18.5 | P |
| Immunohistochemistry (section) | |
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| 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 11/12/2024 MGI 6.24 |
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