SLC35A2

Last Update:2017-12-11

SLC35A2 encodes a UDP-galactose transporter that is localized in the Golgi membrane. It is also known as UGT1. The encoded protein has multiple membrane-spanning regions. UDP-galactose is transported into the Golgi lumen and used as a glycosyl donor for glycan synthesis. It also transports UDP-N-acetylgalactosamine in addition to UDP-galactose. Mutation of SLC35A2 is associated with congenital disorder of glycosylation type 2M.

Keyword: UDP-N-acetylgalactosamine ,  UDP-galactose ,  UGT ,  congenital disorder of glycosylation ,  nucleotide sugar transporter

Nucleotide Sugar Transporter


GGDB Symbol SLC35A2    Alias
DesignationUDP-galactose transporter
OrganismHomo sapiens
GeneID 7355
HGNC SLC35A2 (11022)
mRNA NM_005660
mapXp11.23-p11.22
Protein NP_005651
EC#    
CAZy
GlyCosmos Glycogenes SLC35A2
OMIM 314375
Disease name
GDGDB
Human Protein Atlas ENSG00000102100
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Orthologous Gene

Acceptor Substrates (Reference)

Acceptor Substrates (KEM-C)

Expression

RNA Expression from Human Protein Atlas
This RNA expression data uses "HPA data" from the Human Protein Atlas. Tissue RNA Expression

data available from v22.proteinatlas.org

Expression (Reference)

Gene Ontology

This page does not indicate all of the enzymatic reaction, and expression of "SLC35A2".