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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC35B4
solute carrier family 35 member B4
Chromosome 7 · 7q33
NCBI Gene: 84912Ensembl: ENSG00000205060.12HGNC: HGNC:20584UniProt: Q969S0
29PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
UDP-N-acetylglucosamine transmembrane transporter activityUDP-xylose transmembrane transporter activityprotein bindingUDP-xylose transmembrane transportinsomniagastrointestinal diseasecorneal ulcergastric cancer
✦AI Summary

SLC35B4 (solute carrier family 35 member B4) is a bifunctional nucleotide sugar transporter localized to the endoplasmic reticulum and Golgi apparatus that mediates the transport of UDP-xylose and UDP-N-acetylglucosamine (UDP-GlcNAc) from the cytoplasm into the Golgi lumen 1. The protein contains a critical C-terminal dilysine motif at position 329 required for proper ER localization 2. SLC35B4 functions in glycoconjugate biosynthesis and is glucose-responsive, with expression increasing ~60% upon glucose stimulation in hepatocytes 3. Clinically, SLC35B4 has emerging relevance in multiple disease contexts. In influenza A virus infection, SLC35B4 promotes viral internalization by facilitating UDP-xylose-dependent heparan sulfate biosynthesis, which regulates AGRN proteoglycan homeostasis and affects endocytic machinery 4. In gastric cancer, SLC35B4 is a YAP1 downstream oncogenic target, with elevated expression associated with poor prognosis and enhanced cell proliferation 5. In prostate cancer, a regulatory SNP (rs1646724) in SLC35B4 correlates with increased recurrence and mortality risk, and SLC35B4 downregulation suppresses cancer cell proliferation and invasion 6. Additionally, SLC35B4 deletions have been identified in PHACE syndrome patients, though likely requiring additional genetic factors for disease manifestation 7.

Sources cited
1
SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-GlcNAc; localizes to Golgi apparatus
PMID: 15911612
2
SLC35B4 transports UDP-xylose to promote heparan sulfate biosynthesis and IAV internalization; deficiency reduces influenza A virus replication
PMID: 40130891
3
SLC35B4 is directly transactivated by YAP1 in gastric cancer; high expression associated with poor prognosis
PMID: 31175271
4
Regulatory SNP rs1646724 in SLC35B4 associated with increased prostate cancer recurrence and mortality; SLC35B4 knockdown suppresses cancer cell proliferation
PMID: 29682886
5
SLC35B4 expression increases ~60% upon glucose stimulation in hepatocytes; localizes to Golgi and ER
PMID: 29867058
6
Lysine at position 329 in C-terminal dilysine motif is crucial for SLC35B4 ER localization
PMID: 30458018
7
SLC35B4 deletions identified in PHACE syndrome patients, though not likely singular cause
PMID: 22544659
Disease Associationsⓘ20
insomniaOpen Targets
0.30Weak
gastrointestinal diseaseOpen Targets
0.25Weak
corneal ulcerOpen Targets
0.24Weak
gastric cancerOpen Targets
0.07Suggestive
hepatocellular carcinomaOpen Targets
0.07Suggestive
prostate cancerOpen Targets
0.06Suggestive
neural tube defects, folate-sensitiveOpen Targets
0.04Suggestive
8p23.1 microdeletion syndromeOpen Targets
0.04Suggestive
holoprosencephaly-hypokinesia-congenital contractures syndromeOpen Targets
0.04Suggestive
attention deficit hyperactivity disorderOpen Targets
0.04Suggestive
hereditary attention deficit-hyperactivity disorderOpen Targets
0.04Suggestive
Spina bifida - hypospadiasOpen Targets
0.03Suggestive
spina bifida-hypospadias syndromeOpen Targets
0.03Suggestive
anencephaly 1Open Targets
0.03Suggestive
Isolated anencephaly/exencephalyOpen Targets
0.03Suggestive
dilated cardiomyopathy 1IOpen Targets
0.03Suggestive
tropical spastic paraparesisOpen Targets
0.03Suggestive
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10Open Targets
0.03Suggestive
spina bifidaOpen Targets
0.03Suggestive
intelligenceOpen Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC35D4Shared pathway100%SLC35D3Protein interaction89%AMPD2Protein interaction82%AMPD3Protein interaction82%AMPD1Protein interaction79%SLC35D2Protein interaction76%
Tissue Expression6 tissues
Liver
100%
Brain
99%
Ovary
56%
Heart
36%
Lung
33%
Bone Marrow
32%
Gene Interaction Network
Click a node to explore
SLC35B4SLC35D4SLC35D3AMPD2AMPD3AMPD1SLC35D2
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q969S0
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.87LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.59 [0.41–0.87]
RankingsWhere SLC35B4 stands among ~20K protein-coding genes
  • #12,236of 20,598
    Most Researched29
  • #7,715of 17,882
    Most Constrained (LOEUF)0.87
Genes detectedSLC35B4
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Cellular SLC35B4 promotes internalization during influenza A virus entry.
PMID: 40130891
mBio · 2025
1.00
2
The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine.
PMID: 15911612
J Biol Chem · 2005
0.90
3
Candidate locus analysis for PHACE syndrome.
PMID: 22544659
Am J Med Genet A · 2012
0.80
4
Nucleotide Sugar Transporter SLC35 Family Structure and Function.
PMID: 31462968
Comput Struct Biotechnol J · 2019
0.70
5
A novel YAP1/SLC35B4 regulatory axis contributes to proliferation and progression of gastric carcinoma.
PMID: 31175271
Cell Death Dis · 2019
0.60