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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: RT-PCR
MGI Accession ID: MGI:6450177
Gene symbol: Ndn
Gene name: necdin, MAGE family member
Probe: Ndn-pA, Ndn-pB
Assay notes: Quantitative RT-PCR. For each sample, the number of Ndn cDNA copies was normalized according to relative efficiency of RT determined by the standard cDNA quantification. These data are described in the text.
Results
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
E12.5 E12.5 TS20: embryo Absent 1 µg; total RNA B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
P1 Brain P1 TS27: brain Absent 1 µg; total RNA B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
P1 Hypoth P1 TS27: hypothalamus Absent 1 µg; total RNA B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
P1 Pons P1 TS27: pons Absent 1 µg; total RNA B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
Adult Hypoth P adult TS28: hypothalamus Absent 1 µg; total RNA B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot 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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03/25/2025
MGI 6.24 		The Jackson Laboratory