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Gene Expression Data
Assay Details
Assay
Reference: J:300837 Martin EMMA, et al., Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Hum Mol Genet. 2021 Jan 21;29(22):3662-3678
Assay type: RT-PCR
MGI Accession ID: MGI:6712475
Gene symbol: Wbp11
Gene name: WW domain binding protein 11
Probe: Wbp11-pA, Wbp11-pB
Assay notes: Quantitative RT-PCR. Relative expression is shown normalized to Hprt expression.
Results Image: S4B
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
Wbp11+/+ E10.5 TS17: embryo Present 0.025 µg; total RNA involves: C57BL/6J * FVB/N Not Specified
Wbp11+/- E10.5 TS17: embryo Present (a) 0.025 µg; total RNA involves: C57BL/6J * FVB/N Wbp11em1Gcha/Wbp11+Not Specified
Notes:
(a) Expression in this heterozygote was approximately half (0.53) of that of wild-type littermates.
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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05/14/2024
MGI 6.23 		The Jackson Laboratory