apolipoprotein C2

Summary
Gene Symbol
  • APOC2
Organism
Homo sapiens (human)
NCBI Gene
344
PubChem
344
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Chylomicron
  • Direct protein sequencing
  • Disease variant
  • HDL
  • Hyperlipidemia
  • LDL
  • Lipid degradation
  • Lipid transport
  • Lipoprotein
  • Reference proteome
  • Secreted
  • Sialic acid
  • Signal
  • VLDL
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A024R0T9
  • Apolipoprotein C2
P02655
  • Apolipoprotein C2
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
apolipoprotein C-II
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0111418 familial apolipoprotein C-II deficiency
DOID:1168 familial hyperlipidemia
DOID:2377 multiple sclerosis

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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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