Gene Expression Literature Detail
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Symbol Name ID |
Wdr47
WD repeat domain 47 MGI:2139593 |
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Reference
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J:360974 Bayam E, Tilly P, Collins SC, Rivera Alvarez J, Kannan M, Tonneau L, Brivio E, Rinaldi B, Lecat R, Schwaller N, Cotellessa L, Maddirevula S, Monteiro F, Guardia CM, Kitajima JP, Kok F, Kato M, Hamed AAA, Salih MA, Al Tala S, Hashem MO, Tada H, Saitsu H, Stabile M, Giacobini P, Friant S, Yuksel Z, Nakashima M, Alkuraya FS, Yalcin B, Godin JD, Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome. EMBO Mol Med. 2025 Jan;17(1):129-168 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | 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 | |
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| RT-PCR | |
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| 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 12/10/2024 MGI 6.24 |
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