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Gene Expression Data
Assay Details
Assay
Reference: J:223046 Rieusset A, et al., Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences. PLoS Genet. 2013;9(9):e1003752
Assay type: Western blot
MGI Accession ID: MGI:6450155
Gene symbol: Ndn
Gene name: necdin, MAGE family member
Antibody: anti-Necdin
Detection system: Secondary antibody coupled to horseradish peroxidase
Results
Image: S1B ©

 Sample Information Bands Other Sample Information
Lane AgeStructure 37 kDa Genetic BackgroundMutant Allele(s)Sex Note
WT E12.5 TS20: embryo Present C57BL/6J Not Specified
Ndn+m/-p E12.5 TS20: embryo Absent involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p E12.5 TS20: embryo Weak (a) involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p E12.5 TS20: embryo Absent involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p E12.5 TS20: embryo Weak (a) involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
-/- E12.5 TS20: embryo Absent B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
Notes:
(a) Four out of eight mice exhibited a faint signal (10-20-fold less intense compared to WT).
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
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