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Symbol
Name
ID
Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
MGI:1928738
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Decreased circulating carnitine concentration
Elevated circulating acylcarnitine concentration
Hyperammonemia
Elevated circulating creatine kinase concentration
Elevated creatine kinase after exercise
Elevated circulating hepatic transaminase concentration
Hypoglycemia
Fasting hypoglycemia
Hypoketotic hypoglycemia
Neonatal hypoglycemia
Hypothermia
Hepatic steatosis
Dicarboxylic aciduria
Disease(s) Associated with SLC25A20
carnitine-acylcarnitine translocase deficiency

Mouse Phenotypes
edema
retropleural edema
Availability Mouse Genotype
Slc25a20tm1a(EUCOMM)Wtsi/Slc25a20tm1a(EUCOMM)Wtsi

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
03/19/2024
MGI 6.23
The Jackson Laboratory