Symbol Name ID

Wdr35 WD repeat domain 35 MGI:1921932

Reference

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

Detailed expression data for these assays: 46 results

Indicates gene expression was analyzed but not necessarily detected.

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

Comments: Some of the results are in the supplementary material.