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Gene Expression Data
Assay Details
Assay
Reference: J:272435 Hunter RW, et al., Loss of Dis3l2 partially phenocopies Perlman syndrome in mice and results in up-regulation of Igf2 in nephron progenitor cells. Genes Dev. 2018 Jul 1;32(13-14):903-908
Assay type: RT-PCR
MGI Accession ID: MGI:6507193
Gene symbol: Dis3l2
Gene name: DIS3 like 3'-5' exoribonuclease 2
Probe: Dis3l2-pA, Dis3l2-pB
Assay notes: Assay is quantitative RT-PCR.
Results Image: S6A
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex Note
Wt1 +/+; Dis3.2 11fl/11fl E18.5 TS26: metanephros Strong Not Specified involves: C57BL/6J Dis3l2em2Jtm/Dis3l2em2JtmNot Specified
Dis3.2 +/delta11 E18.5 TS26: metanephros Present Not Specified involves: C57BL/6J Dis3l2em1Jtm/Dis3l2+Not Specified
Dis3.2 delta11/delta11 E18.5 TS26: metanephros Absent Not Specified C57BL/6J-Dis3l2em1Jtm Dis3l2em1Jtm/Dis3l2em1JtmNot Specified
Wt1 Cre/+; Dis3.2 11fl/11fl E18.5 TS26: metanephros Trace Not Specified involves: 129S4/SvJae * C57BL/6J Dis3l2em2Jtm/Dis3l2em2Jtm, Wt1tm1(EGFP/cre)Wtp/Wt1+Not Specified Conditional mutant.
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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04/23/2024
MGI 6.23 		The Jackson Laboratory