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Symbol
Name
ID 		Slc26a2
solute carrier family 26 (sulfate transporter), member 2
MGI:892977
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Edema
Hydrops fetalis
Costal cartilage calcification
Disease(s) Associated with SLC26A2
achondrogenesis type IB
diastrophic dysplasia

Mouse Phenotypes
impaired glucose tolerance
Availability Mouse Genotype
Slc26a2em1(IMPC)Bay/Slc26a2+
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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Funding Information
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Send questions and comments to User Support. 		last database update
03/24/2026
MGI 6.24 		The Jackson Laboratory