Wiki-Pi
Answer Survey
Home
About
Help
Advanced Search
B4GALT3 and ARL15
Number of citations of the paper that reports this interaction (PMID
16169070
)
531
Data Source:
BioGRID
(two hybrid)
HPRD
(two hybrid)
B4GALT3
ARL15
Gene Name
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 3
ADP-ribosylation factor-like 15
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Golgi Membrane
Cytoplasm
Golgi Apparatus
Integral Component Of Membrane
Golgi Cisterna Membrane
Extracellular Vesicular Exosome
Intracellular
Extracellular Vesicular Exosome
Molecular Function
Beta-N-acetylglucosaminylglycopeptide Beta-1,4-galactosyltransferase Activity
N-acetyllactosamine Synthase Activity
Galactosyltransferase Activity
Metal Ion Binding
Molecular_function
GTP 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
Small GTPase Mediated Signal Transduction
Biological_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
Adiponectin levels (
20011104
22479202
)
HDL cholesterol (
20686565
)
Protein-Protein Interactions
3 interactors:
ARL15
SAT1
SURF2
13 interactors:
B4GALT3
CCDC90B
CRMP1
FUNDC2
GAPDH
GRIPAP1
PDE6D
PTN
RPL8
TFG
TUBB2A
UBR1
UNC119
Entrez ID
8703
54622
HPRD ID
04929
12471
Ensembl ID
ENSG00000158850
ENSG00000185305
Uniprot IDs
A8K5Z0
O60512
Q9NXU5
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
Tagcloud
?
Tagcloud (Difference)
?
Tagcloud (Intersection)
?