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Symbol
Name
ID

Slc39a8
solute carrier family 39 (metal ion transporter), member 8
MGI:1914797

Phenotype annotations related to cellular

Darker colors indicate more annotations

Human Phenotypes	Decreased activity of mitochondrial complex II	Decreased activity of mitochondrial complex IV	Decreased activity of the pyruvate dehydrogenase complex
Disease(s) Associated with SLC39A8
congenital disorder of glycosylation type IIn

Mouse Phenotypes		increased fetal cardiomyocyte proliferation
Availability	Mouse Genotype	increased fetal cardiomyocyte proliferation
	Slc39a8^tm1.2Mrl/Slc39a8^tm1.2Mrl

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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