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B3GNT2
Gene Name
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Golgi Membrane
Integral Component Of Membrane
Extracellular Vesicular Exosome
Molecular Function
Galactosyltransferase Activity
N-acetyllactosaminide Beta-1,3-N-acetylglucosaminyltransferase Activity
Biological Process
Carbohydrate Metabolic Process
Protein O-linked Glycosylation
Axon Guidance
Sensory Perception Of Smell
Biological_process
Pathogenesis
O-glycan Processing
Keratan Sulfate Biosynthetic Process
Glycosaminoglycan Metabolic Process
Poly-N-acetyllactosamine Biosynthetic Process
Keratan Sulfate Metabolic Process
Post-translational Protein Modification
Cellular Protein Metabolic Process
Small Molecule Metabolic Process
Pathways
MPS IIIB - Sanfilippo syndrome B
Diseases of glycosylation
Defective B4GALT7 causes EDS, progeroid type
MPS I - Hurler syndrome
Keratan sulfate/keratin metabolism
MPS IX - Natowicz syndrome
Defective SLC26A2 causes chondrodysplasias
Glycosaminoglycan metabolism
O-linked glycosylation
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective CHST14 causes EDS, musculocontractural type
Defective PAPSS2 causes SEMD-PA
MPS IIIA - Sanfilippo syndrome A
Myoclonic epilepsy of Lafora
Glycogen storage diseases
Defective CHST6 causes MCDC1
MPS IIID - Sanfilippo syndrome D
MPS IIIC - Sanfilippo syndrome C
Keratan sulfate biosynthesis
Diseases associated with glycosaminoglycan metabolism
Mucopolysaccharidoses
Post-translational protein modification
Defective EXT2 causes exostoses 2
MPS II - Hunter syndrome
Defective B3GAT3 causes JDSSDHD
Defective CHST3 causes SEDCJD
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
MPS IV - Morquio syndrome A
MPS IV - Morquio syndrome B
Defective CHSY1 causes TPBS
Metabolism of carbohydrates
MPS VII - Sly syndrome
O-linked glycosylation of mucins
MPS VI - Maroteaux-Lamy syndrome
Drugs
Diseases
GWAS
Ankylosing spondylitis (
20062062
)
Rheumatoid arthritis (
22446963
)
Protein-protein Interactions
2 interactors:
C1GALT1C1
TMEM246
Entrez ID
10678
HPRD ID
09279
Ensembl ID
ENSG00000170340
Uniprot IDs
Q9NY97
PDB IDs
Enriched GO Terms of Interacting Partners
?
Platelet Morphogenesis
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