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Symbol
Name
ID
Slc39a8
solute carrier family 39 (metal ion transporter), member 8
MGI:1914797
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Knee flexion contracture
Elbow flexion contracture
Hypotonia
Severe muscular hypotonia
Poor head control
Disease(s) Associated with SLC39A8
congenital disorder of glycosylation type IIn

Mouse Phenotypes
abnormal myocardial trabeculae morphology
thin myocardium compact layer
increased fetal cardiomyocyte proliferation
Availability Mouse Genotype
Slc39a8tm1.2Mrl/Slc39a8tm1.2Mrl

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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory