Symbol Name ID |
Slc2a2
solute carrier family 2 (facilitated glucose transporter), member 2 MGI:1095438 |
Darker colors indicate more annotations |
Human Phenotypes | Muscle weakness |
Disease(s) Associated with SLC2A2 | |
Fanconi syndrome |
Mouse Phenotypes | increased muscle cell glucose uptake |
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Availability | Mouse Genotype | |
Albtm1(cre/ERT2)Mtz/Albtm1(cre/ERT2)Mtz Slc2a2tm2Thor/Slc2a2tm2Thor (conditional) |
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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last database update 04/23/2024 MGI 6.23 |
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