HS6ST3
Heparan-sulfate 6-O-sulfotransferase 3
Also known as: H6ST3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IZP7
- Gene
- HS6ST3
- Ensembl
- ENSG00000185352
- Chromosome
- 13
- Canonical length
- 471 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear membrane,Plasma membrane,Actin filaments
OverviewNCBI Gene
Heparan sulfate (HS) sulfotransferases, such as HS6ST3, modify HS to generate structures required for interactions between HS and a variety of proteins. These interactions are implicated in proliferation and differentiation, adhesion, migration, inflammation, blood coagulation, and other diverse processes (Habuchi et al., 2000 [PubMed 10644753]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
471 residues, UniProt reviewed canonical sequence.
>Q8IZP7|HS6ST3
1 MDERFNKWLL TPVLTLLFVV IMYQYVSPSC TSSCTNFGEQ PRAGEAGPPA VPGPARRAQA
61 PPEEWERRPQ LPPPPRGPPE GPRGAAAPEE EDEEPGDPRE GEEEEEEDEP DPEAPENGSL
121 PRFVPRFNFS LKDLTRFVDF NIKGRDVIVF LHIQKTGGTT FGRHLVKNIR LEQPCSCKAG
181 QKKCTCHRPG KKETWLFSRF STGWSCGLHA DWTELTNCVP AIMEKKDCPR NHSHTRNFYY
241 ITMLRDPVSR YLSEWKHVQR GATWKTSLHM CDGRSPTPDE LPTCYPGDDW SGVSLREFMD
301 CTYNLANNRQ VRMLADLSLV GCYNLTFMNE SERNTILLQS AKNNLKNMAF FGLTEFQRKT
361 QFLFERTFNL KFISPFTQFN ITRASNVEIN EGARQRIEDL NFLDMQLYEY AKDLFQQRYH
421 HTKQLEHQRD RQKRREERRL QREHRDHQWP KEDGAAEGTV TEDYNSQVVR WLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HS6ST3 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 16 nTPM
- hippocampal formation: 10 nTPM
- hypothalamus: 6.6 nTPM
- blood vessel: 6.1 nTPM
- basal ganglia: 5.4 nTPM
- amygdala: 5 nTPM
Single-cell type
- oligodendrocyte progenitor cells: 1,363 nCPM
- adrenal medulla cells: 1,362 nCPM
- retinal ganglion cells: 1,317 nCPM
- brain excitatory neurons: 1,267 nCPM
- pancreatic islet cells: 1,236 nCPM
- bergmann glia: 1,233 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hippocampal formation: 45 nTPM
- cerebral cortex: 38 nTPM
- hypothalamus: 32 nTPM
- midbrain: 30 nTPM
- thalamus: 23 nTPM
- basal ganglia: 22 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)
- 0.22
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.19
- DepMap mean gene effect
- 0.09
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HS6ST3 as an antibody target. Whether an autoantibody or antibody against HS6ST3 could matter depends on whether native HS6ST3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HS6ST3 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 HS6ST3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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