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Symbol
Name
ID

Slc25a21
solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21
MGI:2445059

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Elevated urinary quinolinic acid level	Lacticaciduria
Disease(s) Associated with SLC25A21	Elevated urinary quinolinic acid level	Lacticaciduria
mitochondrial DNA depletion syndrome 18

Mouse Phenotypes		decreased circulating LDL cholesterol level	decreased circulating magnesium level	decreased circulating potassium level	decreased circulating alanine transaminase level	decreased circulating aspartate transaminase level
Availability	Mouse Genotype	decreased circulating LDL cholesterol level	decreased circulating magnesium level	decreased circulating potassium level	decreased circulating alanine transaminase level	decreased circulating aspartate transaminase level
	Slc25a21^{tm1a(KOMP)Wtsi}/Slc25a21^{tm1a(KOMP)Wtsi}
	Slc25a21^{tm1d(KOMP)Wtsi}/Slc25a21^{tm1d(KOMP)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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