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Symbol
Name
ID

Slc39a4
solute carrier family 39 (zinc transporter), member 4
MGI:1919277

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Impaired T cell function	Decreased serum zinc	Low alkaline phosphatase	Decreased serum testosterone concentration
Disease(s) Associated with SLC39A4
acrodermatitis enteropathica

Mouse Phenotypes		decreased intestinal iron level	increased fasting circulating glucose level	abnormal copper level	decreased intestine copper level	decreased liver copper level	increased liver copper level	increased liver iron level	abnormal mineral homeostasis	abnormal zinc homeostasis
Availability	Mouse Genotype	decreased intestinal iron level	increased fasting circulating glucose level	abnormal copper level	decreased intestine copper level	decreased liver copper level	increased liver copper level	increased liver iron level	abnormal mineral homeostasis	abnormal zinc homeostasis
	Slc39a4^{tm1.1(KOMP)Wtsi}/Slc39a4⁺
	Slc39a4^tm2Gka/Slc39a4^tm2Gka Tg(Vil1-cre/ERT2)23Syr/0 (conditional)

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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