Atp5a1 ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 [ Mus musculus (house mouse) ]
Source: NCBI Gene (ID 11946)
Source: NCBI Gene (ID 11946)
Symbol: Atp5a1
Full name: ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Mus musculus
Also known as: Atp5f1a; Atpm; D18Ertd206e; Mom2
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]
Expression: Ubiquitous expression in heart adult (RPKM 1425.7), kidney adult (RPKM 741.8) and 28 other tissues
Orthologs: human
Gene size: 9102bp
Exon count: 12