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UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Summary
- UniProt ID
- Q9H3H5
- Gene Symbol
-
- DPAGT1
- DPAGT2
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9H3H5
- PubChem
- Q9H3H5
- The Human Metabolome Database
- HMDBP01096
- The O-GlcNAc Database
- Q9H3H5
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Congenital disorder of glycosylation
- Congenital myasthenic syndrome
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Glycosyltransferase
- Magnesium
- Metal-binding
- Reference proteome
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| protein N-linked glycosylation |
| UDP-N-acetylglucosamine metabolic process |
| dolichol-linked oligosaccharide biosynthetic process |
| GO Term |
|---|
| membrane |
| intracellular membrane-bounded organelle |
| endoplasmic reticulum membrane |
Sequence
MWAFSELPMPLLINLIVSLLGFVATVTLIPAFRGHFIAARLCGQDLNKTSRQQIPESQGVISGAVFLIILFCFIPFPFLNCFVKEQCKAFPHHEFVALIGALLAICCMIFLGFADDVLNLRWRHKLLLPTAASLPLLMVYFTNFGNTTIVVPKPFRPILGLHLDLGILYYVYMGLLAVFCTNAINILAGINGLEAGQSLVISASIIVFNLVELEGDCRDDHVFSLYFMIPFFFTTLGLLYHNWYPSRVFVGDTFCYFAGMTFAVVGILGHFSKTMLLFFMPQVFNFLYSLPQLLHIIPCPRHRIPRLNIKTGKLEMSYSKFKTKSLSFLGTFILKVAESLQLVTVHQSETEDGEFTECNNMTLINLLLKVLGPIHERNLTLLLLLLQILGSAITFSIRYQLVRLFYDV
Glycosylation Sites
G83460ZZ
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | Homo sapiens |
| Defective DPAGT1 causes CDG-1j, CMSTA2 | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080470 | developmental and epileptic encephalopathy 36 | |
| DOID:0080562 | congenital disorder of glycosylation Ij | |
| DOID:0110676 | congenital myasthenic syndrome 13 | |
| DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
| DOID:0111375 | fetal akinesia deformation sequence syndrome | |
| DOID:0111377 | fetal akinesia deformation sequence syndrome 1 | |
| DOID:1029 | familial periodic paralysis | |
| DOID:10534 | stomach cancer | |
| DOID:1059 | intellectual disability |
