SLC35D3
Solute carrier family 35 member D3
Also known as: FRCL1, S35D3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5M8T2
- Gene
- SLC35D3
- Ensembl
- ENSG00000182747
- Chromosome
- 6
- Canonical length
- 416 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Centriolar satellite
OverviewNCBI Gene
Enables UDP-glucose transmembrane transporter activity. Involved in UDP-glucose transmembrane transport. Is active in synaptic vesicle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
416 residues, UniProt reviewed canonical sequence.
>Q5M8T2|SLC35D3
1 MRQLCRGRVL GISVAIAHGV FSGSLNILLK FLISRYQFSF LTLVQCLTSS TAALSLELLR
61 RLGLIAVPPF GLSLARSFAG VAVLSTLQSS LTLWSLRGLS LPMYVVFKRC LPLVTMLIGV
121 LVLKNGAPSP GVLAAVLITT CGAALAGAGD LTGDPIGYVT GVLAVLVHAA YLVLIQKASA
181 DTEHGPLTAQ YVIAVSATPL LVICSFASTD SIHAWTFPGW KDPAMVCIFV ACILIGCAMN
241 FTTLHCTYIN SAVTTSFVGV VKSIATITVG MVAFSDVEPT SLFIAGVVVN TLGSIIYCVA
301 KFMETRKQSN YEDLEAQPRG EEAQLSGDQL PFVMEELPGE GGNGRSEGGE AAGGPAQESR
361 QEVRGSPRGV PLVAGSSEEG SRRSLKDAYL EVWRLVRGTR YMKKDYLIEN EELPSPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC35D3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 10
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 5.7 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 5.7 nTPM
- hypothalamus: 3 nTPM
- midbrain: 1.2 nTPM
- adrenal gland: 0.9 nTPM
- stomach: 0.5 nTPM
- colon: 0.4 nTPM
Single-cell type
- megakaryocytes: 50 nCPM
- platelets: 18 nCPM
- other brain neurons: 4.8 nCPM
- pancreatic islet cells: 3.1 nCPM
- brain inhibitory neurons: 2.5 nCPM
- megakaryocyte progenitors: 2.4 nCPM
Immune cell
- total PBMC: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- hypothalamus: 13 nTPM
- thalamus: 12 nTPM
- basal ganglia: 7.9 nTPM
- midbrain: 4.7 nTPM
- medulla oblongata: 1.2 nTPM
- amygdala: 0.9 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.87
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 1.07
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- energy homeostasis
- platelet dense granule organization
- positive regulation of autophagy
- positive regulation of protein exit from endoplasmic reticulum
- protein exit from endoplasmic reticulum
- transmembrane transport
- UDP-glucose transmembrane transport
Molecular functions
- antiporter activity
- protein-macromolecule adaptor activity
- UDP-glucose transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC35D3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC35D3 as an antibody target. Whether an autoantibody or antibody against SLC35D3 could matter depends on whether native SLC35D3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC35D3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SLC35D3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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