SLC35F2: Solute Carrier Family 35 Member F2

A nucleotide-sugar transporter with emerging roles in cancer and glycosylation

Gene Information Card

Symbol SLC35F2
Full Name Solute Carrier Family 35 Member F2
Gene Type Protein coding
Chromosomal Location 11q23.1
NCBI Gene ID 54733 ncbi.nlm.nih.gov/gene/54733
Ensembl ID ENSG00000110651
UniProt ID Q8IXU6
OMIM ID 618425
HGNC ID 20773
Aliases HSS1, MGC13170, dJ248O5.1

Description

SLC35F2 encodes a member of the solute carrier family 35 (SLC35) of nucleotide-sugar transporters. These proteins are localized to the Golgi apparatus and endoplasmic reticulum and mediate the transport of nucleotide sugars into the lumen, which is essential for proper glycosylation of proteins and lipids. SLC35F2 has been implicated in cancer cell proliferation and chemoresistance, and its expression is altered in several malignancies.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal cancer Overexpression of SLC35F2 is associated with increased cell proliferation and poor prognosis; may modulate glycosylation pathways affecting tumor progression. PubMed: 25636840
Gastric cancer Upregulation of SLC35F2 correlates with lymph node metastasis and advanced TNM stage; potential biomarker. PubMed: 27323851
Hepatocellular carcinoma SLC35F2 knockdown reduces cell viability and induces apoptosis; linked to altered N-glycosylation. PubMed: 30323247

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 14.2 Medium
Kidney 11.8 Medium
Colon 9.5 Low
Lung 8.1 Low
Breast 6.3 Low
Cell Line Expression
Cell Line nTPM Notes
HepG2 (liver cancer) 15.0 High expression
HT-29 (colorectal cancer) 12.4 Moderate expression
A549 (lung cancer) 7.8 Low expression
MCF7 (breast cancer) 5.2 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.104G>A (p.Arg35His) Missense <0.01% (gnomAD) Unknown; predicted benign by SIFT
c.487C>T (p.Arg163Trp) Missense <0.01% (gnomAD) Unknown; predicted possibly damaging by PolyPhen-2
c.832_833insA Frameshift <0.01% (COSMIC) Loss of function; truncation
Mutation functional classification

Loss of Function (LOF)

Frameshift insertions (e.g., c.832_833insA) are predicted to cause premature truncation and loss of transporter activity.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in SLC35F2.

Dominant Negative (DN)

No evidence for dominant-negative effects.

Gene Ontology (GO)

• GO:0000139~Golgi membrane • GO:0005459~UDP-galactose transmembrane transporter activity
• GO:0015780~UDP-galactose transport • GO:0015781~UDP-N-acetylglucosamine transport
• GO:0015782~UDP-glucose transport

Pathways

Nucleotide-sugar transport (Reactome: R-HSA-425407)
Glycosylation of proteins (Reactome: R-HSA-446203)

Protein Summary

SLC35F2 is a multi-pass transmembrane protein localized to the Golgi apparatus. It functions as a nucleotide-sugar transporter, likely mediating the import of UDP-galactose, UDP-N-acetylglucosamine, and UDP-glucose into the Golgi lumen. This activity is critical for the biosynthesis of glycoproteins and glycolipids. The protein consists of 10 predicted transmembrane domains and is expressed in various tissues, with highest levels in liver and kidney. Altered expression has been linked to cancer progression and chemoresistance.

Related Products

Product name Cat.No. Species Gene ID
SLC35F2 Knockout HEK293 Cell Line EDJ-KQ12029 Human 54733 Details Get a Quote
SLC35F2 Knockout HCT 116 Cell Line EDC08637 Human 54733 Details Get a Quote
SLC35F2 Knockout A-549 Cell Line EDJ-KQ40637 Human 54733 Details Get a Quote
SLC35F2 Knockout HeLa Cell Line EDJ-KQ40639 Human 54733 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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