Homo sapiens Protein: B3GNT4
Summary
InnateDB Protein IDBP-62256.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol B3GNT4
Protein Name UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000319636
InnateDB Gene IDBG-62254 (B3GNT4)
Protein Structure
UniProt Annotation
Function Has a beta-1,3-N-acetylglucosaminyltransferase activity for type 2 oligosaccharides.
Subcellular Localization Golgi apparatus membrane {ECO:0000250}; Single-pass type II membrane protein {ECO:0000250}.
Disease Associations
Tissue Specificity Mainly expressed in brain tissues such as whole brain, hippocampus, amygdala, cerebellum and caudate nucleus. Also expressed in colon, esophagus and kidney. {ECO:0000269PubMed:11042166}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0008378 galactosyltransferase activity
GO:0016757 transferase activity, transferring glycosyl groups
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0006486 protein glycosylation
GO:0016266 O-glycan processing
GO:0018146 keratan sulfate biosynthetic process
GO:0030203 glycosaminoglycan metabolic process
GO:0042339 keratan sulfate metabolic process
GO:0043687 post-translational protein modification
GO:0044267 cellular protein metabolic process
GO:0044281 small molecule metabolic process
Cellular Component
GO:0000139 Golgi membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR002659 Glycosyl transferase, family 31
IPR003378 Fringe-like
PFAM PF01762
PF02434
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9C0J1
PhosphoSite PhosphoSite-Q9C0J1
TrEMBL A0A024RBT1
UniProt Splice Variant
Entrez Gene 79369
UniGene Hs.363315
RefSeq NP_110392
HUGO HGNC:15683
OMIM 605864
CCDS CCDS9227
HPRD 12058
IMGT
EMBL AB049586 AF321825 AJ130848 AJ278962 AK095746 AL834452 AY358940 BC031399 CH471054
GenPept AAH31399 AAL37219 AAQ89299 BAB21532 BAC04622 CAC45045 CAC82375 CAD39112 EAW98308 EAW98309