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B6.CB-Slc38a8em1Lmon/Cnbc Strain Detail
Summary
  • Strain Name
    B6.CB-Slc38a8em1Lmon/Cnbc
  • Attributes
    congenic, endonuclease-mediated mutation, mutant strain
  • MGI ID
    MGI:7618766
  • Other IDs
    EM:15349
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Mutation Carried Marker
Slc38a8em1Lmon Slc38a8
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
EM:15349 EMMA B6.CB-Slc38a8em1Lmon/Cnbc exact match to ID
References
  • Earliest
    J:343795 Guardia A, et al., A Slc38a8 Mouse Model of FHONDA Syndrome Faithfully Recapitulates the Visual Deficits of Albinism Without Pigmentation Defects. Invest Ophthalmol Vis Sci. 2023 Oct 3;64(13):32
  • 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
01/06/2026
MGI 6.24 		The Jackson Laboratory