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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: Immunohistochemistry
MGI Accession ID: MGI:5613237
Gene symbol: Wdr35
Gene name: WD repeat domain 35
Antibody: Wdr35 085
Detection system: Secondary antibody coupled to Alexa Fluor 594
Results
Specimen 2E: embryonic day 13.5 (more )
Note: Double labeled with acetylated alpha-Tubulin (green).
Structure Level Pattern Image Note
TS21: metanephros Present 2E
Specimen 2F: embryonic day 13.5 (more )
Note: Double labeled with acetylated alpha-Tubulin (green).
Structure Level Pattern Image Note
TS21: choroid plexus Present 2F
Specimen 2G: embryonic day 11.5 (more )
Note: Confocal image. Double labeled with acetylated alpha-Tubulin (green).
Structure Level Pattern Image Note
TS19: limb mesenchyme Present 2G
Specimen 2H: embryonic day 11.5; Wdr35yeti/Wdr35yeti (more )
Note: Confocal image. Double labeled with acetylated alpha-Tubulin (green).
Structure Level Pattern Image Note
TS19: limb mesenchyme Absent 2H
Specimen S4 D: embryonic day 14.5 (more )
Note: Confocal image. Double labeled with acetylated alpha-Tubulin (green). E,F are higher magnifications.
Structure Level Pattern Image Note
TS22: lobar bronchus epithelium Present S4F , S4D , S4E
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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03/25/2025
MGI 6.24 		The Jackson Laboratory