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Symbol
Name
ID

Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
MGI:1928738

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Hepatomegaly
Disease(s) Associated with SLC25A20	Hepatomegaly
carnitine-acylcarnitine translocase deficiency

Mouse Phenotypes		embryo cyst
Availability	Mouse Genotype	embryo cyst
	Slc25a20^{tm1a(EUCOMM)Wtsi}/Slc25a20^{tm1a(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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