Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10678
Gene name Gene Name - the full gene name approved by the HGNC.
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
B3GNT2
Synonyms (NCBI Gene) Gene synonyms aliases
3-Gn-T1, 3-Gn-T2, B3GN-T2, B3GNT, B3GNT-2, B3GNT1, BETA3GNT, BGNT2, BGnT-2, beta-1, beta3Gn-T1, beta3Gn-T2
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p15
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II transmembrane protein. It prefers the substrate of lacto-N-neotetraose, and is involved in the biosynthesis of poly-N-acetyllactosamine chains. Two
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022296 hsa-miR-124-3p Microarray 18668037
MIRT023499 hsa-miR-1-3p Microarray 18668037
MIRT303046 hsa-miR-10a-3p PAR-CLIP 20371350
MIRT089117 hsa-miR-5583-3p PAR-CLIP 20371350
MIRT089105 hsa-miR-15a-5p PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane TAS
GO:0005515 Function Protein binding IPI 18826941
GO:0005794 Component Golgi apparatus IBA 21873635
GO:0006486 Process Protein glycosylation IBA 21873635
GO:0007411 Process Axon guidance IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605581 15629 ENSG00000170340
Protein
UniProt ID Q9NY97
Protein name N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 (EC 2.4.1.149) (Beta-1,3-N-acetylglucosaminyltransferase 1) (BGnT-1) (Beta-1,3-Gn-T1) (Beta3Gn-T1) (Beta-1,3-galactosyltransferase 7) (Beta-1,3-GalTase 7) (Beta3Gal-T7) (Beta3GalT7) (b3Gal-T
Protein function Beta-1,3-N-acetylglucosaminyltransferase involved in the synthesis of poly-N-acetyllactosamine. Catalyzes the initiation and elongation of poly-N-acetyllactosamine chains. Shows a marked preference for Gal(beta1-4)Glc(NAc)-based acceptors (PubMe
PDB 6WMM , 6WMN , 6WMO , 7JHK , 7JHL , 7JHM , 7JHN , 7JHO , 8SZ3 , 8TIC , 8TJC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01762 Galactosyl_T 156 351 Galactosyltransferase Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11042166}.
Sequence
MSVGRRRIKLLGILMMANVFIYFIMEVSKSSSQEKNGKGEVIIPKEKFWKISTPPEAYWN
REQEKLNRQYNPILSMLTNQTGEAGRLSNISHLNYCEPDLRVTSVVTGFNNLPDRFKDFL
LYLRCRNYSLLIDQPDKCAKKPFLLLAIKSLTPHFARRQAIRESWGQESNAGNQTVVRVF
LLGQTPPEDNHPDLSDMLKFESEKHQDILMWNYRDTFFNLSLKEVLFLRWVSTSCPDTEF
VFKGDDDVFVNTHHILNYLNSLSKTKAKDLFIGDVIHNAGPHRDKKLKYYIPEVVYSGLY
PPYAGGGGFLYSGHLALRLYHITDQVHLYPIDDVYTGMCLQKLGLVPEKHK
GFRTFDIEE
KNKNNICSYVDLMLVHSRKPQEMIDIWSQLQSAHLKC
Sequence length 397
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Glycosaminoglycan biosynthesis - keratan sulfate
Glycosphingolipid biosynthesis - lacto and neolacto series
Metabolic pathways
  Keratan sulfate biosynthesis
O-linked glycosylation of mucins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13 rs119463990, rs587777813, rs398123555, rs119463996, rs587777748, rs119463991, rs119463992, rs119464997, rs267606814, rs119463989, rs533916138, rs587777815, rs200198778, rs267606969, rs267606963
View all (138 more)
23877401
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 22446963
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
23904455
Unknown
Disease term Disease name Evidence References Source
Muscular dystrophy muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13 GenCC
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 23577190, 23904455
Autoimmune Diseases Associate 23904455
Carcinogenesis Stimulate 35073841
Carcinoma Hepatocellular Associate 25605193
Colonic Neoplasms Associate 27004849
Colorectal Neoplasms Associate 15620693, 27004849
Esophageal Neoplasms Associate 35073841
Genetic Diseases Inborn Associate 33494994
Glioblastoma Associate 27871300
Graves Disease Associate 23904455