Full name: solute carrier family 35 member D1

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: SHNKND; UGTREL7

Summary: Glycosylation of cellular glycoconjugates occurs in the endoplasmic reticulum (ER) and Golgi compartment, and requires transport of nucleotide sugars from the cytosol into the lumen of the ER and Golgi by specific transporters. The protein encoded by this gene resides in the ER, and transports both UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylgalactosamine (UDP-GalNAc) from the cytoplasm to the ER lumen. It may participate in glucuronidation and/or chondroitin sulfate biosynthesis. Mutations in this gene are associated with Schneckenbecken dysplasia.[provided by RefSeq, Sep 2009]

Expression: Ubiquitous expression in liver (RPKM 14.1), colon (RPKM 11.9) and 24 other tissues

Gene size: 81173bp

Exon count: 19