Beta-1,3-galactosyltransferase 6

Summary
UniProt ID
Q96L58
Gene Symbol
  • B3GALT6
Organism
Homo sapiens (human)
External Links
GlyConnect
GlyGen
Q96L58
PubChem
Q96L58
The Human Metabolome Database
HMDBP03281
Annotation
Keyword
  • Disease variant
  • Dwarfism
  • Ehlers-Danlos syndrome
  • Glycoprotein
  • Glycosyltransferase
  • Golgi apparatus
  • Manganese
  • Reference proteome
  • Signal-anchor
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MKLLRRAWRRRAALGLGTLALCGAALLYLARCAAEPGDPRAMSGRSPPPPAPARAAAFLAVLVASAPRAAERRSVIRSTWLARRGAPGDVWARFAVGTAGLGAEERRALEREQARHGDLLLLPALRDAYENLTAKVLAMLAWLDEHVAFEFVLKADDDSFARLDALLAELRAREPARRRRLYWGFFSGRGRVKPGGRWREAAWQLCDYYLPYALGGGYVLSADLVHYLRLSRDYLRAWHSEDVSLGAWLAPVDVQREHDPRFDTEYRSRGCSNQYLVTHKQSLEDMLEKHATLAREGRLCKREVQLRLSYVYDWSAPPSQCCQRREGIP
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
131 N-linked (GlcNAc...) asparagine
308
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 2 entries
Pathway Name Organism
A tetrasaccharide linker sequence is required for GAG synthesis Homo sapiens
Defective B3GALT6 causes EDSP2 and SEMDJL1 Homo sapiens
Disease
Displaying entries 21 - 30 of 76 in total
DO ID Disease Name Source
DOID:0080332 bicuspid aortic valve disease
DOID:0080333 aortic valve disease 1
DOID:0080334 aortic valve disease 2
DOID:0110106 atrial heart septal defect 1
DOID:0110107 atrial heart septal defect 2
DOID:0110108 atrial heart septal defect 3
DOID:0110109 atrial heart septal defect 4
DOID:0110110 atrial heart septal defect 5
DOID:0110111 atrial heart septal defect 6
DOID:0110112 atrial heart septal defect 7

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024