exostosin glycosyltransferase 2
| UniProt | Protein Name |
|---|---|
| Q93063 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| polysaccharide biosynthetic process | ||
| ossification | ||
| mesoderm formation | ||
| chondrocyte differentiation | ||
| glycosaminoglycan biosynthetic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi membrane | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum | ||
| Golgi apparatus | ||
| Golgi apparatus |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| acetylglucosaminyltransferase activity | ||
| glucuronosyltransferase activity | ||
| glycosyltransferase activity | ||
| glycosyltransferase activity |
| Gene Ontology |
|---|
| heparan sulfate proteoglycan biosynthetic process |
| transferase activity |
| InterPro |
|---|
| Exostosin, GT47 domain |
| Exostosin-like |
| Glycosyl transferase 64 domain |
| Nucleotide-diphospho-sugar transferases |
| 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 |
| Disease ID | Disease Name |
|---|---|
| ORPHA:52022 |
|
| ORPHA:466926 |
|
| ORPHA:321 |
|
| OMIM:616682 |
|
| OMIM:133701 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: December 8, 2025