About   Help   FAQ
Symbol
Name
ID
Slc2a2
solute carrier family 2 (facilitated glucose transporter), member 2
MGI:1095438
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Muscle weakness
Disease(s) Associated with SLC2A2
Fanconi syndrome

Mouse Phenotypes
increased muscle cell glucose uptake
Availability Mouse Genotype
Albtm1(cre/ERT2)Mtz/Albtm1(cre/ERT2)Mtz
Slc2a2tm2Thor/Slc2a2tm2Thor  (conditional)

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