SLC35D2
Nucleotide sugar transporter SLC35D2
Also known as: S35D2_HUMAN, SQV7L, UGTrel8
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q76EJ3
- Gene
- SLC35D2
- Ensembl
- ENSG00000130958
- Chromosome
- 9
- Canonical length
- 337 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
337 residues, UniProt reviewed canonical sequence.
>Q76EJ3|SLC35D2
1 MTAGGQAEAE GAGGEPGAAR LPSRVARLLS ALFYGTCSFL IVLVNKALLT TYGFPSPIFL
61 GIGQMAATIM ILYVSKLNKI IHFPDFDKKI PVKLFPLPLL YVGNHISGLS STSKLSLPMF
121 TVLRKFTIPL TLLLETIILG KQYSLNIILS VFAIILGAFI AAGSDLAFNL EGYIFVFLND
181 IFTAANGVYT KQKMDPKELG KYGVLFYNAC FMIIPTLIIS VSTGDLQQAT EFNQWKNVVF
241 ILQFLLSCFL GFLLMYSTVL CSYYNSALTT AVVGAIKNVS VAYIGILIGG DYIFSLLNFV
301 GLNICMAGGL RYSFLTLSSQ LKPKPVGEEN ICLDLKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC35D2 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
- 7
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 62 nTPM
- duodenum: 61 nTPM
- liver: 53 nTPM
- colon: 46 nTPM
- rectum: 44 nTPM
- stomach: 41 nTPM
Single-cell type
- oligodendrocytes: 144 nCPM
- microglia: 67 nCPM
- proximal tubule cells: 62 nCPM
- hepatocytes: 52 nCPM
- bergmann glia: 31 nCPM
- distal convoluted tubule cells: 28 nCPM
Immune cell
- T-reg: 3.9 nTPM
- memory CD8 T-cell: 2.9 nTPM
- memory CD4 T-cell: 2.1 nTPM
- non-classical monocyte: 2.1 nTPM
- NK-cell: 1.8 nTPM
- MAIT T-cell: 1.7 nTPM
Brain region
- white matter: 41 nTPM
- medulla oblongata: 39 nTPM
- pons: 31 nTPM
- thalamus: 28 nTPM
- basal ganglia: 27 nTPM
- midbrain: 25 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)
- 1.6
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.49
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- antiporter activity
- nucleotide-sugar transmembrane transporter activity
- UDP-glucuronate transmembrane transporter activity
- UDP-N-acetylgalactosamine transmembrane transporter activity
- UDP-N-acetylglucosamine transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC35D2 as an antibody target. Whether an autoantibody or antibody against SLC35D2 could matter depends on whether native SLC35D2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC35D2 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 SLC35D2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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