ATP synthase F1 subunit alpha

Summary
Gene Symbol
  • ATP5F1A
Organism
Homo sapiens (human)
NCBI Gene
498
PubChem
498
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Acetylation
  • Alternative splicing
  • CF(1)
  • Cell membrane
  • Direct protein sequencing
  • Disease variant
  • Glycoprotein
  • Hydrogen ion transport
  • Membrane
  • Methylation
  • Mitochondrion inner membrane
  • Phosphoprotein
  • Primary mitochondrial disease
  • Reference proteome
  • Transit peptide
Proteins
Displaying all 2 entries
UniProt Protein Name
P25705
  • ATP synthase F1 subunit alpha
V9HW26
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 8 entries
DO ID Disease Name Source
DOID:0070461 mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
DOID:0070462 mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
DOID:0080208 metabolic dysfunction-associated steatotic liver disease
DOID:0111498 combined oxidative phosphorylation deficiency 22
DOID:10652 Alzheimer's disease
DOID:10763 hypertension
DOID:6432 pulmonary hypertension
DOID:8725 vascular dementia

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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: February 17, 2025