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Gene Expression Data
Assay Details
Assay
Reference: J:171617 Mill P, et al., 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
Assay type: RNA in situ
MGI Accession ID: MGI:5613225
Gene symbol: Wdr35
Gene name: WD repeat domain 35
Probe: Wdr35 5' probe
Probe preparation: Antisense RNA
Assay notes: The authors did not specify which probe was used, either this 5' or a 3' probe: MGI:5613224.
Results
Specimen 1M wild-type: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: embryo Present 1M Wdr35+/+

Specimen 1M yeti: embryonic day 10.5; Wdr35yeti/Wdr35yeti (more )
Structure Level Pattern Image Note
TS17: embryo Present 1M Wdr35yet/yet The authors state that the mutant transcripts were subject to nonsense-mediated decay.


Contributing Projects:
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
03/25/2025
MGI 6.24
The Jackson Laboratory