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Symbol
Name
ID
Magt1
magnesium transporter 1
MGI:1914325
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Mediastinal lymphadenopathy
Splenomegaly
Hepatomegaly
Disease(s) Associated with MAGT1
congenital disorder of glycosylation Icc
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia


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
04/09/2024
MGI 6.23
The Jackson Laboratory