apolipoprotein A5

Summary
Gene Symbol
  • APOA5
Organism
Homo sapiens (human)
NCBI Gene
116519
PubChem
116519
Alliance of Genome Resources
Annotation
Keyword
  • Chylomicron
  • Coiled coil
  • Disease variant
  • Endosome
  • Golgi apparatus
  • HDL
  • Lipid transport
  • Lipoprotein
  • Phosphoprotein
  • Reference proteome
  • Secreted
  • Signal
  • VLDL
Proteins
Displaying all 2 entries
UniProt Protein Name
Q6Q788
  • Apolipoprotein A5
  • Regeneration-associated protein 3
A0A0B4RUS7
  • Apolipoprotein A5
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Apolipoprotein Eb
Functional Category
  • L: Replication, recombination and repair
  • N: Cell motility
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:0111421 familial apolipoprotein A5 deficiency
DOID:1171 hyperlipoproteinemia type V
DOID:1172 hyperlipoproteinemia type IV
DOID:1459 hypothyroidism
DOID:3393 coronary artery disease
DOID:3526 cerebral infarction
DOID:9352 type 2 diabetes mellitus

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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