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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: RT-PCR
MGI Accession ID: MGI:5613233
Gene symbol: Wdr35
Gene name: WD repeat domain 35
Results
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
tm2a/tm2a E9.5 TS15: embryo Absent Not Specified involves: C57BL/6N Wdr35tm2a(EUCOMM)Hmgu/Wdr35tm2a(EUCOMM)HmguNot Specified
tm2a/tm2a E9.5 TS15: embryo Absent Not Specified involves: C57BL/6N Wdr35tm2a(EUCOMM)Hmgu/Wdr35tm2a(EUCOMM)HmguNot Specified
+/tm2a E9.5 TS15: embryo Present Not Specified involves: C57BL/6N Wdr35tm2a(EUCOMM)Hmgu/Wdr35+Not Specified
+/+ E9.5 TS15: embryo Present Not Specified involves: C57BL/6N Not Specified
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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12/17/2024
MGI 6.24 		The Jackson Laboratory