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B6.129S1-Ndntm2Stw Strain Detail
Summary
  • Strain Name
    B6.129S1-Ndntm2Stw
  • Attributes
    congenic, mutant strain, targeted mutation
  • MGI ID
    MGI:6450218
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Ndntm2Stw Ndn
References
  • Earliest
    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
  • All
    1
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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
03/24/2026
MGI 6.24 		The Jackson Laboratory