CHST10
Carbohydrate sulfotransferase 10
Also known as: CHSTA_HUMAN, HNK-1ST
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43529
- Gene
- CHST10
- Ensembl
- ENSG00000115526
- Chromosome
- 2
- Canonical length
- 356 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This protein encoded by this gene transfers sulfate to the C-3 hydroxyl of terminal glucuronic acid of protein- and lipid-linked oligosaccharides. This protein was first identified as a sulfotransferase that acts on the human natural killer-1 (HNK-1) glycan; HNK-1 is a carbohydrate involved in neurodevelopment and synaptic plasticity.[provided by RefSeq, Feb 2011]
Canonical amino-acid sequenceUniProt
356 residues, UniProt reviewed canonical sequence.
>O43529|CHST10
1 MHHQWLLLAA CFWVIFMFMV ASKFITLTFK DPDVYSAKQE FLFLTTMPEV RKLPEEKHIP
61 EELKPTGKEL PDSQLVQPLV YMERLELIRN VCRDDALKNL SHTPVSKFVL DRIFVCDKHK
121 ILFCQTPKVG NTQWKKVLIV LNGAFSSIEE IPENVVHDHE KNGLPRLSSF SDAEIQKRLK
181 TYFKFFIVRD PFERLISAFK DKFVHNPRFE PWYRHEIAPG IIRKYRRNRT ETRGIQFEDF
241 VRYLGDPNHR WLDLQFGDHI IHWVTYVELC APCEIMYSVI GHHETLEDDA PYILKEAGID
301 HLVSYPTIPP GITVYNRTKV EHYFLGISKR DIRRLYARFE GDFKLFGYQK PDFLLNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHST10 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
- 1
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 29 nTPM
- basal ganglia: 24 nTPM
- amygdala: 20 nTPM
- hippocampal formation: 17 nTPM
- cerebellum: 16 nTPM
- midbrain: 13 nTPM
Single-cell type
- astrocytes: 29 nCPM
- pituicytes/fscs: 25 nCPM
- bergmann glia: 19 nCPM
- oligodendrocyte progenitor cells: 17 nCPM
- epididymal efferent duct absorptive cells: 16 nCPM
- müller glia: 16 nCPM
Immune cell
- gdT-cell: 1.3 nTPM
- plasmacytoid DC: 1.1 nTPM
- memory CD8 T-cell: 1 nTPM
- memory B-cell: 0.8 nTPM
- naive CD8 T-cell: 0.7 nTPM
- naive B-cell: 0.6 nTPM
Brain region
- cerebral cortex: 45 nTPM
- thalamus: 35 nTPM
- basal ganglia: 34 nTPM
- hippocampal formation: 31 nTPM
- midbrain: 31 nTPM
- amygdala: 31 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)
- 0.95
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.98
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- androgen metabolic process
- carbohydrate biosynthetic process
- cell adhesion
- estrogen metabolic process
- learning
- long-term memory
- protein O-linked glycosylation
- proteoglycan biosynthetic process
Molecular functions
- sulfotransferase activity
- HNK-1 sulfotransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CHST10 as an antibody target. Whether an autoantibody or antibody against CHST10 could matter depends on whether native CHST10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHST10 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 CHST10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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