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B4GALT3
Gene Name
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 3
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Golgi Membrane
Cytoplasm
Golgi Apparatus
Integral Component Of Membrane
Golgi Cisterna Membrane
Extracellular Vesicular Exosome
Molecular Function
Beta-N-acetylglucosaminylglycopeptide Beta-1,4-galactosyltransferase Activity
N-acetyllactosamine Synthase Activity
Galactosyltransferase Activity
Metal Ion Binding
Biological Process
Carbohydrate Metabolic Process
Pathogenesis
Keratan Sulfate Biosynthetic Process
Protein N-linked Glycosylation Via Asparagine
Glycosaminoglycan Metabolic Process
Keratan Sulfate Metabolic Process
Post-translational Protein Modification
Cellular Protein Metabolic Process
Small Molecule Metabolic Process
Pathways
Keratan sulfate/keratin metabolism
MPS I - Hurler syndrome
MPS IX - Natowicz syndrome
Glycosaminoglycan metabolism
Defective MGAT2 causes MGAT2-CDG (CDG-2a)
N-Glycan antennae elongation
Defective CHST14 causes EDS, musculocontractural type
N-glycan antennae elongation in the medial/trans-Golgi
Myoclonic epilepsy of Lafora
MPS IIID - Sanfilippo syndrome D
Defective CHST6 causes MCDC1
Glycogen storage diseases
Keratan sulfate biosynthesis
Defective ALG2 causes ALG2-CDG (CDG-1i)
Diseases associated with glycosaminoglycan metabolism
Mucopolysaccharidoses
Defective ALG3 causes ALG3-CDG (CDG-1d)
Post-translational protein modification
Defective EXT2 causes exostoses 2
Asparagine N-linked glycosylation
MPS IV - Morquio syndrome A
Defective MPDU1 causes MPDU1-CDG (CDG-1f)
Metabolism of carbohydrates
Diseases associated with N-glycosylation of proteins
MPS VI - Maroteaux-Lamy syndrome
MPS IIIB - Sanfilippo syndrome B
Diseases of glycosylation
Defective B4GALT7 causes EDS, progeroid type
Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS)
Defective SLC26A2 causes chondrodysplasias
Transport to the Golgi and subsequent modification
Defective ALG1 causes ALG1-CDG (CDG-1k)
Defective MOGS causes MOGS-CDG (CDG-2b)
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective ALG9 causes ALG9-CDG (CDG-1l)
Defective PAPSS2 causes SEMD-PA
Defective MAN1B1 causes MRT15
MPS IIIA - Sanfilippo syndrome A
Defective ALG11 causes ALG11-CDG (CDG-1p)
MPS IIIC - Sanfilippo syndrome C
Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2
MPS II - Hunter syndrome
Defective CHST3 causes SEDCJD
Defective B3GAT3 causes JDSSDHD
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective RFT1 causes RFT1-CDG (CDG-1n)
Defective ALG6 causes ALG6-CDG (CDG-1c)
Defective ALG8 causes ALG8-CDG (CDG-1h)
Defective ALG12 causes ALG12-CDG (CDG-1g)
Defective CHSY1 causes TPBS
MPS IV - Morquio syndrome B
MPS VII - Sly syndrome
Drugs
Diseases
GWAS
Protein-protein Interactions
3 interactors:
ARL15
SAT1
SURF2
Entrez ID
8703
HPRD ID
04929
Ensembl ID
ENSG00000158850
Uniprot IDs
A8K5Z0
O60512
PDB IDs
Enriched GO Terms of Interacting Partners
?
Spermidine Acetylation
Putrescine Catabolic Process
Oxalate Transport
3'-phosphoadenosine 5'-phosphosulfate Biosynthetic Process
Polyamine Catabolic Process
Neurotransmitter Uptake
3'-phosphoadenosine 5'-phosphosulfate Metabolic Process
Polyamine Biosynthetic Process
Amine Biosynthetic Process
Polyamine Metabolic Process
Sulfate Transmembrane Transport
Sulfate Transport
Neutral Amino Acid Transport
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