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Symbol
Name
ID
Slc39a4
solute carrier family 39 (zinc transporter), member 4
MGI:1919277
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Alopecia of scalp
Hypogeusia
Disease(s) Associated with SLC39A4
acrodermatitis enteropathica

Mouse Phenotypes
abnormal craniofacial development
Availability Mouse Genotype
Slc39a4tm1Gka/Slc39a4+

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
04/30/2024
MGI 6.23
The Jackson Laboratory