Symbol Name ID |
Wdr35
WD repeat domain 35 MGI:1921932 |
Reference
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J:171617 Mill P, Lockhart PJ, Fitzpatrick E, Mountford HS, Hall EA, Reijns MA, Keighren M, Bahlo M, Bromhead CJ, Budd P, Aftimos S, Delatycki MB, Savarirayan R, Jackson IJ, Amor DJ, Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis. Am J Hum Genet. 2011 Apr 8;88(4):508-15 |
Age | E9.5 | E10.5 | E11.5 | E13.5 | E14.5 |
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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