GEL complex subunit OPTI

Summary
UniProt ID
Q9BUV8
Gene Symbol
  • C20orf24
  • OPTI
  • PNAS-11
  • RAB5IF
  • RCAF1
Gene ID
55969
Organism
Homo sapiens (human)
GlyGen
Q9BUV8
PubChem
Q9BUV8
The O-GlcNAc Database
Q9BUV8
O-GlcNAcAtlas
Q9BUV8
Re-Glyco
Q9BUV8
Annotation
Keyword
  • Alternative splicing
  • Disease variant
  • Endoplasmic reticulum
  • Intellectual disability
  • Mitochondrion inner membrane
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Gene Ontology (GO)
Subcellular Location(GO Annotation)

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

Sequence
MSGGRRKEEPPQPQLANGALKVSVWSKVLRSDAAWEDKDEFLDVIYWFRQIIAVVLGVIWGVLPLRGFLGIAGFCLINAGVLYLYFSNYLQIDEEEYGGTWELTKEGFMTSFALFMVCVADSFTTGHLDHLLHCHPL
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
26
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Complex IV assembly Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:0081125 craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2

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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: April 6, 2026