Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
heparan sulfate-glucosamine 3-sulfotransferase 6

Summary
Gene Symbol
  • HS3ST6
Organism
Homo sapiens (human)
External Links
NCBI Gene
64711
GGDB ID
HGNC
14178
map
  • 16p13.3
OMIM
KEGG Gene ID
hsa:64711
PubChem
64711
Alliance of Genome Resources
Annotation
Keyword
  • Disulfide bond
  • Glycoprotein
  • Golgi apparatus
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q96QI5
  • Heparan sulfate D-glucosaminyl 3-O-sulfotransferase 6
Annotation information from UniProt.
Gene Ontology (GO)
Displaying all 2 entries
GO Term Evidence Code PMID
blastocyst hatching
heparan sulfate proteoglycan biosynthetic process, enzymatic modification
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
GlycoGene Database (GGDB)
GGDB ID
gg237
Gene Symbol
  • HS3ST6
KEGG BRITE Database
Orthology
K09679
Name
[heparan sulfate]-glucosamine 3-sulfotransferase 6 [EC:2.8.2.-]
References
Rhea

RHEA:15461

3'-phosphoadenylyl sulfate
H+ + adenosine 3',5'-bisphosphate
Enzyme
PMID
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:10316 pneumoconiosis
DOID:10320 asbestosis
DOID:10324 anthracosilicosis
DOID:10328 siderosis
DOID:12522 bagassosis
DOID:14735 hereditary angioedema
DOID:8566 herpes simplex
The Human Phenotype Ontology
Displaying all 8 entries
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000282 Facial edema
HP:0002014 Diarrhea
HP:0002027 Abdominal pain
HP:0002572 Episodic vomiting
HP:0007514 Edema of the dorsum of hands
HP:0012027 Laryngeal edema
HP:0100665 Angioedema
Displaying 1 entry
Disease ID Disease Name
OMIM:619367
  • angioedema, hereditary, 8
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying entries 1 - 10 of 52 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
3564879 WB:WBGene00044303
32918 FB:FBgn0031005
102366195 LATCH08486
797517 ZFIN:ZDB-GENE-090312-176 DANRE17817
103030517 ASTMX11890
108254972 ICTPU24929
108258330 ICTPU21104
113573247 ELEEL12809
106589565 SALSA98663
106609741 SALSA65511
About Release Notes Help Feedback

Click here to visit the beta site.

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.0.0

Last updated: August 19, 2024