OnlineIMD
Sulfate transporter deficiency
Type
Disease
External link(s)
IEMbase
Gene
SLC26A2
/ Solute Carrier Family 26 Member 2
5q32
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Sulfate anion transporter
Disease group(s)
18.2.3 Disorders of glycosaminoglycan synthesis and O-xylosylation
Child entries
Multiple epiphyseal dysplasia type 4
Atelosteogenesis type 2
Achondrogenesis type 1B
Diastrophic dysplasia