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Symbol Name ID |
Slc22a5
solute carrier family 22 (organic cation transporter), member 5 MGI:1329012 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased circulating carnitine concentration |
Hyperammonemia |
Elevated circulating creatine kinase concentration |
Elevated circulating alanine aminotransferase concentration |
Elevated circulating aspartate aminotransferase concentration |
Recurrent hypoglycemia |
Impaired gluconeogenesis |
Dehydration |
Decreased carnitine level in liver |
Microvesicular hepatic steatosis |
Reduced muscle carnitine level |
Dicarboxylic aciduria |
Ketosis |
| Disease(s) Associated with SLC22A5 | |||||||||||||
| systemic primary carnitine deficiency disease |
| Mouse Phenotypes | decreased circulating carnitine level |
aminoaciduria |
increased circulating ammonia level |
hypoglycemia |
abnormal glucose homeostasis |
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| 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) |
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last database update 04/30/2024 MGI 6.23 |
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