exostosin glycosyltransferase 2

Summary
Gene Symbol
  • EXT2
Aliases
  • Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase
  • N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase
  • SOTV
Organism
Homo sapiens (human)
NCBI Gene
2132
GGDB ID
HGNC
3513
mRNA
map
  • 11p12-p11
Protein
OMIM
KEGG Gene ID
hsa:2132
PubChem
2132
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Disease variant
  • Disulfide bond
  • Endoplasmic reticulum
  • Epilepsy
  • Glycoprotein
  • Glycosyltransferase
  • Golgi apparatus
  • Hereditary multiple exostoses
  • Intellectual disability
  • Manganese
  • Metal-binding
  • Reference proteome
  • Secreted
  • Signal-anchor
  • Transmembrane helix
  • Tumor suppressor
Proteins
Displaying 1 entry
UniProt Protein Name
Q93063
  • Exostosin glycosyltransferase 2
  • Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase
  • Heparan sulfate co-polymerase subunit EXT1
  • Multiple exostoses protein 2
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
exostosin
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
GlycoGene Database (GGDB)
GGDB ID
gg159
Gene Symbol
  • EXT2
Reactions
Displaying entries 1 - 5 of 20 in total
Donor Acceptor Reducing terminal(Acceptor) Reference
UDP-GalNAc
G14371GV
O-(Gly)Ser-Glu mixture of EXT1 and EXT2
UDP-GalNAc
G99041PQ
O-C2H4NHCbz mixture of EXT1 and EXT2
UDP-GalNAc
G14371GV
O-Ser mixture of EXT1 and EXT2
UDP-GalNAc
G14371GV
O-Ser-Gly-Typ-Pro-Asp-Gly mixture of EXT1 and EXT2
UDP-GalNAc
G99041PQ
O-C2H4NHCbz
Orthologous Gene
KEGG BRITE Database
Orthology
K02367
Name
glucuronyl/N-acetylglucosaminyl transferase EXT2 [EC:2.4.1.224 2.4.1.225]
References
Reactions
Displaying all 2 entries
KEGG Reaction Enzyme Acceptor Product
R05935
R10138
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:206 hereditary multiple exostoses
The Human Phenotype Ontology
Displaying entries 1 - 10 of 132 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0000016 Urinary retention
HP:0000028 Cryptorchidism
HP:0000054 Micropenis
HP:0000077 Abnormality of the kidney
HP:0000093 Proteinuria
HP:0000248 Brachycephaly
HP:0000252 Microcephaly
HP:0000256 Macrocephaly
Displaying all 5 entries
Disease ID Disease Name
ORPHA:52022
  • Potocki-Shaffer syndrome
OMIM:616682
  • seizures-scoliosis-macrocephaly syndrome
ORPHA:466926
  • seizures-scoliosis-macrocephaly syndrome
ORPHA:321
  • hereditary multiple osteochondromas
OMIM:133701
  • exostoses, multiple, type 2
Ortholog
Displaying entries 81 - 83 of 83 in total
Species Gene ID OrthoDB Alliance of Genome Resources Orthologous MAtrix
122201128 PANLE14332
123799595 URSAM08630
129007272 9600_0:002ccd

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024