1. Gene
  2. Atp5a1 - ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 Gene

Atp5a1 - ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 Gene

Mus musculus

Also known as Atpm; Mom2; Atp5f1a; D18Ertd206e

Gene ID: 11946 | Gene type: protein coding

About Atp5a1

Summary

Enables ATP binding activity and proton-transporting ATP Synthase activity, rotational mechanism. Acts upstream of or within lipid metabolic process. Located in membrane and mitochondrion. Is expressed in several structures, including alimentary system; integumental system; nervous system; respiratory system; and sensory organ. Human ortholog(s) of this gene implicated in combined Oxidative Phosphorylation deficiency 22 and mitochondrial complex V (ATP Synthase) deficiency nuclear type 4. Orthologous to human ATP5F1A (ATP Synthase F1 subunit alpha). [provided by Alliance of Genome Resources, Apr 2022]

Atp5a1 Products(1)

mRNA Protein Name
NM_007505.2 NP_031531.1 ATP synthase subunit alpha, mitochondrial precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables ATP binding IMP
IMP: Inferred from mutant phenotype
7916601 MGI
enables protein binding IPI
IPI: Inferred from physical interaction
19941651 MGI
enables proton-transporting ATP synthase activity, rotational mechanism IMP
IMP: Inferred from mutant phenotype
17612527 MGI
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within embryo development IMP
IMP: Inferred from mutant phenotype
17387143 MGI
acts upstream of or within lipid metabolic process IMP
IMP: Inferred from mutant phenotype
17612527 MGI
Cellular Component GO Annotation Evidence Reference Source
located in membrane IMP
IMP: Inferred from mutant phenotype
20080761 MGI
located in mitochondrion IDA
IDA: Inferred from direct assay
19808025 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

ATP synthase subunit alpha, mitochondrial

ATP synthase F1 subunit alpha

modifier of Min 2