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MONB 8, MONB 15 Primer Detail
Primers
  • Name
    MONB 8, MONB 15
  • ID
    MGI:1329489
  • Region Covered
    coding region
Genes
Slc22a5 solute carrier family 22 (organic cation transporter), member 5
Polymorphisms
J:51918 Nezu J, et al., Nat Genet. 1999 Jan;21(1):91-4
Endonuclease Gene Allele Fragments Strains
CfrI3I Slc22a5 a one band C3.OH-H2o2, C57BL/6
j two bands C3.OH-H2o2 Slc22a5jvs, C57BL/6-Slc22a5jvs
References
J:51918 Nezu J, et al., Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter. Nat Genet. 1999 Jan;21(1):91-4
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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11/05/2024
MGI 6.24 		The Jackson Laboratory