coenzyme Q2, polyprenyltransferase

Summary
Gene Symbol
  • COQ2
Organism
Homo sapiens (human)
NCBI Gene
27235
PubChem
27235
Alliance of Genome Resources
Annotation
Keyword
  • Alternative initiation
  • Alternative splicing
  • Disease variant
  • Isoprene biosynthesis
  • Mitochondrion inner membrane
  • Neurodegeneration
  • Parkinsonism
  • Primary mitochondrial disease
  • Reference proteome
  • Transferase
  • Transit peptide
  • Transmembrane helix
  • Ubiquinone biosynthesis
Proteins
Displaying 1 entry
UniProt Protein Name
Q96H96
  • 4-hydroxybenzoate decaprenyltransferase
  • COQ2 homolog
  • Para-hydroxybenzoate--polyprenyltransferase
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
4-hydroxybenzoate
Functional Category
  • C: Energy production and conversion
  • G: Carbohydrate transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0050730 coenzyme Q10 deficiency disease
DOID:0070238 primary coenzyme Q10 deficiency 1
DOID:10603 glucose intolerance
DOID:1184 nephrotic syndrome
DOID:4752 multiple system atrophy

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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