ORTHOLOGY: K02126 Help
Entry
Symbol
ATPeF0A, MTATP6, ATP6
Name
F-type H+-transporting ATPase subunit a
Pathway
map05022 Pathways of neurodegeneration - multiple diseases
map05208 Chemical carcinogenesis - reactive oxygen species
Module
M00158 F-type ATPase, eukaryotes
Disease
H00068 Leber hereditary optic atrophy
H01177 Infantile bilateral striatal necrosis
H01369 ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:ko00001 ]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
09150 Organismal Systems
09159 Environmental adaptation
04714 Thermogenesis
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
09164 Neurodegenerative disease
05010 Alzheimer disease
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
05012 Parkinson disease
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
05014 Amyotrophic lateral sclerosis
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
05016 Huntington disease
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
05020 Prion disease
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
05022 Pathways of neurodegeneration - multiple diseases
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
Mitochondrial biogenesis [BR:ko03029 ]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial DNA-encoded proteins
F-type ATPase
K02126 ATPeF0A, MTATP6, ATP6; F-type H+-transporting ATPase subunit a
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Genes
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Taxonomy UniProt
Reference
Authors
Burrage LC, Tang S, Wang J, Donti TR, Walkiewicz M, Luchak JM, Chen LC, Schmitt ES, Niu Z, Erana R, Hunter JV, Graham BH, Wong LJ, Scaglia F
Title
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 gene.
Journal
Sequence