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B10.C-H7b/(47N)Sn Strain Detail
Summary
  • Strain Name
    B10.C-H7b/(47N)Sn
  • Attributes
    congenic, minor histocompatibility congenic
  • MGI ID
    MGI:2160851
  • Synonyms
    B10.C(47N), B10.C/(47N)
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
H7
References
  • Earliest
    J:5170 Meier H, et al., A neurological mutation (msd) of the mouse causing a deficiency of myelin synthesis. Exp Brain Res. 1970 Jun 25;10(5):512-25
  • All
    22
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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Funding Information
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory