Symbol Name ID |
Slc22a5
solute carrier family 22 (organic cation transporter), member 5 MGI:1329012 |
Darker colors indicate more annotations |
Human Phenotypes | Dicarboxylic aciduria |
Disease(s) Associated with SLC22A5 | |
systemic primary carnitine deficiency disease |
Mouse Phenotypes | aminoaciduria |
abnormal renal reabsorption |
|
Availability | Mouse Genotype | ||
Slc22a5jvs/Slc22a5jvs |
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 07/05/2024 MGI 6.24 |
|
|