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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC35D3
solute carrier family 35 member D3
Chromosome 6 · 6q23.3
NCBI Gene: 340146Ensembl: ENSG00000182747.5HGNC: HGNC:15621UniProt: B7Z9Y0
8PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
UDP-glucose transmembrane transporter activityUDP-glucose transmembrane transportsynaptic vesicle membraneprotein bindingneurodegenerative diseasediverticular diseasetype 2 diabetes mellitusdiabetes mellitus
✦AI Summary

SLC35D3 is a solute carrier transporter with multiple distinct functions across different cell types and subcellular compartments. In neurons, SLC35D3 localizes to synaptic vesicles and functions as a vesicular transporter for UDP-glucose 1, suggesting a role in neurotransmission and neuromodulation. SLC35D3 also regulates dopamine signaling by controlling the plasma membrane localization of dopamine receptor D1 (D1R) through its localization to the endoplasmic reticulum and early endosomes 2. Mutations in SLC35D3 impair D1R trafficking and cause metabolic syndrome in mice, characterized by obesity and reduced dopaminergic signaling in striatal neurons; this phenotype is reversible with D1R agonist administration 2. In megakaryocytes and platelets, SLC35D3 is critical for dense granule biogenesis and hemostasis, though the precise molecular mechanism remains unclear 3, 4. Clinically, SLC35D3 mRNA expression in lymph nodes serves as a biomarker for detecting colorectal cancer metastases and predicting patient recurrence risk and prognosis 5, 6, 7. Collectively, SLC35D3 functions as both a nucleotide sugar transporter and a trafficking regulator essential for neural dopamine signaling and hematopoietic homeostasis.

Sources cited
1
SLC35D3 localizes to synaptic vesicles and functions as a vesicular transporter for UDP-glucose
PMID: 34269178
2
SLC35D3 mutations cause metabolic syndrome and impaired dopamine signaling by disrupting D1R membrane localization; phenotype is reversible with D1R agonist
PMID: 24550737
3
SLC35D3 mutations regulate platelet dense granule contents and are a cause of isolated delta-storage pool deficiency
PMID: 17062724
4
SLC35D3 is enriched in early endosomes and required for platelet dense granule biogenesis during megakaryocyte differentiation
PMID: 22611153
5
SLC35D3 mRNA analysis improves detection of colorectal cancer lymph node metastases compared with routine histopathology
PMID: 34192710
6
SLC35D3 mRNA in the ColoNode biomarker panel identifies colorectal cancer patients at high risk of recurrence, with superior performance to histopathology alone
PMID: 37700602
7
SLC35D3 is expressed in colorectal cancer epithelial tumor cells and has prognostic value when combined with other biomarkers for predicting recurrent disease
PMID: 32049988
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.32Weak
diverticular diseaseOpen Targets
0.29Weak
type 2 diabetes mellitusOpen Targets
0.27Weak
diabetes mellitusOpen Targets
0.25Weak
Abnormality of the skeletal systemOpen Targets
0.19Weak
musculoskeletal system diseaseOpen Targets
0.09Suggestive
obesityOpen Targets
0.08Suggestive
spondylolisthesisOpen Targets
0.08Suggestive
PainOpen Targets
0.07Suggestive
ThrombocytopeniaOpen Targets
0.04Suggestive
thrombocytopenia 4Open Targets
0.04Suggestive
metabolic syndromeOpen Targets
0.04Suggestive
colorectal adenocarcinomaOpen Targets
0.04Suggestive
lung carcinomaOpen Targets
0.03Suggestive
colorectal cancerOpen Targets
0.03Suggestive
neoplasmOpen Targets
0.02Suggestive
osteosarcomaOpen Targets
0.02Suggestive
cancerOpen Targets
0.01Suggestive
Colon Sessile Serrated Adenoma/PolypOpen Targets
0.01Suggestive
Hermansky-Pudlak syndromeOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC35A3Protein interaction96%SLC35B2Protein interaction92%SLC35A1Protein interaction92%SLC35B4Protein interaction89%SLC35B3Protein interaction85%SLC35B1Protein interaction80%
Tissue Expression6 tissues
Brain
100%
Bone Marrow
22%
Lung
0%
Heart
0%
Ovary
0%
Liver
0%
Gene Interaction Network
Click a node to explore
SLC35D3SLC35A3SLC35B2SLC35A1SLC35B4SLC35B3SLC35B1
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q5M8T2
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.54LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.09 [0.79–1.54]
RankingsWhere SLC35D3 stands among ~20K protein-coding genes
  • #17,708of 20,598
    Most Researched8
  • #15,416of 17,882
    Most Constrained (LOEUF)1.54
Genes detectedSLC35D3
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
CEACAM5, KLK6, SLC35D3, POSTN, and MUC2 mRNA Analysis Improves Detection and Allows Characterization of Tumor Cells in Lymph Nodes of Patients Who Have Colon Cancer.
PMID: 34192710
Dis Colon Rectum · 2021
1.00
2
Localization, proteomics, and metabolite profiling reveal a putative vesicular transporter for UDP-glucose.
PMID: 34269178
Elife · 2021
0.90
3
Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons.
PMID: 24550737
PLoS Genet · 2014
0.80
4
The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules.
PMID: 17062724
Blood · 2007
0.70
5
qRT-PCR analysis of CEACAM5, KLK6, SLC35D3, MUC2 and POSTN in colon cancer lymph nodes-An improved method for assessment of tumor stage and prognosis.
PMID: 37700602
Int J Cancer · 2024
0.60