About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory