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Symbol
Name
ID
Slc25a13
solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13
MGI:1354721
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Elevated plasma citrulline
Hypertyrosinemia
Hyperlysinemia
Hypermethioninemia
Hyperthreoninemia
Hyperargininemia
Hyperbilirubinemia
Conjugated hyperbilirubinemia
Increased serum bile acid concentration
Decreased HDL cholesterol concentration
Hypercholesterolemia
Hypertriglyceridemia
Hyperammonemia
Elevated circulating alanine aminotransferase concentration
Elevated circulating aspartate aminotransferase concentration
Elevated gamma-glutamyltransferase level
Elevated circulating alkaline phosphatase concentration
Cerebral edema
Hepatic steatosis
Macrovesicular hepatic steatosis
Microvesicular hepatic steatosis
Argininosuccinic aciduria
Disease(s) Associated with SLC25A13
adult-onset type II citrullinemia
neonatal-onset type II citrullinemia

Mouse Phenotypes
abnormal amino acid level
hypoglycemia
decreased circulating insulin level
abnormal gluconeogenesis
increased liver triglyceride level
abnormal urine homeostasis
Availability Mouse Genotype
Slc25a13tm1Lct/Slc25a13tm1Lct
Slc25a13tm1Lct/Slc25a13+

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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory