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MIRAGE
Dehydrodolichyl diphosphate synthase complex subunit NUS1

Summary
UniProt ID
Q96E22
Gene Symbol
  • C6orf68
  • NGBR
  • NUS1
Gene ID
116150
Organism
Homo sapiens (human)
GlyGen
Q96E22
PubChem
Q96E22
The Human Metabolome Database
HMDBP09222
Re-Glyco
Q96E22
Annotation
Keyword
  • 3D-structure
  • Angiogenesis
  • Congenital disorder of glycosylation
  • Developmental protein
  • Differentiation
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Intellectual disability
  • Lipid metabolism
  • Magnesium
  • Metal-binding
  • Receptor
  • Reference proteome
  • Transferase
  • Transmembrane helix
Gene Ontology (GO)
Displaying all 2 entries
GO Term
dehydrodolichyl diphosphate synthase complex
endoplasmic reticulum membrane
Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Annotation information from UniProt.
Sequence
MTGLYELVWRVLHALLCLHRTLTSWLRVRFGTWNWIWRRCCRAASAAVLAPLGFTLRKPPAVGRNRRHHRHPRGGSCLAAAHHRMRWRADGRSLEKLPVHMGLVITEVEQEPSFSDIASLVVWCMAVGISYISVYDHQGIFKRNNSRLMDEILKQQQELLGLDCSKYSPEFANSNDKDDQVLNCHLAVKVLSPEDGKADIVRAAQDFCQLVAQKQKRPTDLDVDTLASLLSSNGCPDPDLVLKFGPVDSTLGFLPWHIRLTEIVSLPSHLNISYEDFFSALRQYAACEQRLGK
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
144 N-linked (GlcNAc...) asparagine
271 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 2 entries
Pathway Name Organism
Defective DHDDS causes RP59 Homo sapiens
Synthesis of Dolichyl-phosphate Homo sapiens
Disease
Displaying all 2 entries
DO ID Disease Name Source
DOID:0080227 autosomal dominant intellectual developmental disorder 55
DOID:0080553 congenital disorder of glycosylation Iaa
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 4, 2025